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% al VOLUME 66
Number 1
Journal of the MARCH, 1976
ASHINGTON
ACADEMY... SCIENCES
Issued Quarterly
at Washington, D.C.
Symposium
Issue
MAY 2 1 1876
LIBRARIES
CONTENTS
Symposium — Energy Recovery from Solid Waste
Editorial . . 195
MAURICE J. WILSON aaa DAVID W. SWINDLE, ie : The Markets aS
and the Economics of Heat Energy from Solid Waste Incineration . 197
G.M. MALLAN and E.I. TITLOW: Energy and Resource Recovery from
Solid Wastes . - (207
B. VINCENT VISCOMI: Bee elie Study foe Burning BefiseWecived
Fuel in the District of Columbia by Potomaé Electric Power Company 217
DAVID KLUMB: Union Electric Company’s Solid Waste Utilization
System .. 225
WALTER K. MACADAM: Desens pad Polos Cantenl Features of ihe
Saugus, Massachusetts Steam Generating Refuse — Energy Plant . . 235
R.G. KISPERT, S.E. SADEK and D.L. WISE: An Evaluation of Methane
Production from Solid Waste. . . 245
R.C. RIGHELATO, F.K.E. IMRIE and " J. VLITOS: Production of
Single Cell Protein from Agricultural and Food Processing Wastes . 257
CHARLES J. ROGERS: Problems and Potential Associated with the
Production of Protein from Cellulosic Wastes . . 271
L.A. SPANO, J. MEDEIROS and M. MANDELS: Bieymatic Hydrolysis
of Polelocie Wastes to Glucose . . sane
JOHN T. PFEFFER and JON C. LIEBMAN: Beery oa Retace by
Bioconversion, Fermentation and Residue Disposal Processes . . . 295
E.R. MOATS: Goodyear Tire-Fired Boiler bie Rese ae ae Vea fs. RUN ee * ears
Book reviews . Sees ee
a - a A a a a -
Previously Published in Resource Recovery and Conservation
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Filer fe ear 9
ENERGY FROM WASTE BY
USING PYROLYSIS
Use our experience. We design and supply.
PYROLYSIS PLANTS:
e for the production of diesel fuel or heating oil
from old tyres and rubber waste
e for the recovery of metal from old cables using
minimal energy
e for the purification and safe reuse of sludge and
mixed polymers
Demonstrations using your own samples are given
in our plants.
=RBOLD PYROLYSE GMBH & Co, RECYCLING KG, Griiner Weg 5, 75 KARLSRUHE, G.F.R.
=
Now available, thoroughly rewritten and up-dated:
NORGANIC CHEMISTRY
A GUIDE TO ADVANCED STUDY
|
_ COMPLETELY REVISED SUCCESSOR TO HESLOP/ROBINSON, INORGANIC CHEMISTRY
|y R.B. HESLOP, Senior Lecturer in Chemistry and K. JONES, Lecturer
ly Chemistry, The University of Manchester institute of Science and
Technology
176. viii + 830 pages. £ 8.90/US $17.95/ Comments and Reviews
| 1. 49.00. ISBN 0-444-41426-6 Inorganic Chemistry, Heslop/Robinson:
find this a superb book and “This top-notch text is now even better!”’
‘7 only highly recommend it Prof. J.H. Day, Ohio University
use.” “An excellent book - indeed | found it so eee
/(of. Oliver Carrier Jr.,
|| Aversity of Mississippi, Prof. Kurt Niedenzu,
that | immediately adopted it as aclass text...
\dical Center
University of Kentucky
he amount of information presented i in readable form in this volume is astonishing...... certain to remain a
i indard text for many years.’ Talanta
b
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| AIMS AND SCOPE
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Resource Recovery and Conservation, 1 (1976) 195 195
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
Editorial
This issue is the Proceedings of a symposium, “‘Energy Recovery from Solid
Wastes’”’ held at the University of Maryland, March 13, 14, 1975. It was the
fourth in a series entitled, ‘““Science and the Environment”’ organized by the
Washington Academy of Sciences. The symposium was sponsored by the
Academy, the Chemical Society of Washington (the Washington, D.C. Section
of the American Chemical Society), the National Center for Resource Re-
covery, Inc. and Committee K-38, Resource Recovery, of the American Society
for Testing and Materials.
The utilization of solid wastes as a source of energy, particularly in storable
and transportable forms, can supply a portion of a nation’s energy needs. This
proportion may appear to be small, of the order of say two percent of U.S.
daily needs, but even this order of magnitude is large when compared with
some other alternative sources which are perhaps less readily available for
development and exploitation.
The purpose of the symposium was to review the state of the art and
practice of energy recovery from the organic portion of a variety of solid
wastes. The emphasis was on processing wastes to some other forms of energy
storage, ranging from solid fuel substitutes for coal to gaseous mixtures for
fuel to chemicals and proteins. This emphasis did not ignore the direct burning
of wastes to raise steam, which is less common in the U.S. than in Europe and
Japan. However, the current research interest in the U.S. (and elsewhere) is
toward fuels (and other products) prepared to a specification, rather than the
utilization of unprocessed mixed wastes in an incinerator. Energy conservation
possibly accruing from utilization of recovered materials (e.g., metals, glass,
paper and plastics) was not addressed.
This proceedings is simultaneously published as an issue of Resource
Recovery and Conservation and of the Journal of the Washington Academy of
Sciences. The editors wish to thank Dr. Richard H. Foote, editor of the
Journal for his assistance. The three editors thank the authors and organizers
for making the symposium possible.
J.G.A.
H.A.
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Resource Recovery and Conservation, 1 (1976) 197—206 197
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
THE MARKETS FOR AND THE ECONOMICS OF HEAT ENERGY FROM
SOLID WASTE INCINERATION*
MAURICE J. WILSON and DAVID W. SWINDLE, JR.
I.C. Thomasson & Associates, Inc., Nashville, Tenn. 37204 (U.S.A.)
(Received 24th March, 1975)
ABSTRACT
This study reviews the disposal and composition of solid waste with respect to its
material and energy resources. It evaluates the economics of front-end materials resource
recovery and the fluctuating markets for specific components, the energy extraction by
conventional incineration, and steam production not only for process needs but also for
coolant and/or heating. It touches briefly on energy recovery in the form of off-gas and
liquids from pyrolyzers, shredding to provide “‘fluff’’, and pelletizing.
MAXIMIZING RESOURCE RECOVERY FROM SOLID WASTE
The term “‘recycling”’ is used often these days, usually in the context which
leads one to believe that recycling of products has been going on for a long
time, wherever and whenever an economic incentive exists.
Today, we frequently hear words or expressions such as pollution, pollution
abatement, “‘urban ore’’, “‘cash for trash’’, solid waste, material resource recovery,
landfills, dumps, etc. Some undoubtedly will prove to be ephemeral; others
will live as long as our society demands.
We cannot engage in rancid rationalization. When we discuss solid waste
management, we should examine and evaluate the economic advantages of
material and energy resource recovery. Market strategies of consumer-oriented
companies have contributed to the amount of solid waste, perhaps excessively
at times with the no deposit—no return throwaways, individual packaging, etc.,
but the consumer is usually delighted with these innovative packaging methods
and the conveniences associated with them. He perhaps does not realize that
it may add to the price which he pays for the particular item.
We generate an ever-increasing quantity of solid waste. Approximately one-
half by weight is a renewable resource such as paper with a relatively high
calorific content. If all the 113,375,000 metric tons of residential and
commercial waste disposed of yearly were incinerated and the heat recovered,
* Paper presented at the Symposium “‘Energy Recovery from Solid Waste”, March 13—14,
1975.
198
this would amount to less than 2 percent of our total prime energy needs or
less than 6 percent of the heat energy required for heating and cooling our
residential and commercial buildings. Incineration of solid waste alleviates
the disposal problem. It has several advantages when compared with landfill
disposal. These are: (1) volume reduction by approximately 90 percent; (2)
sterile residue (ash) for which several uses exist; (3) recovery of heat which can
be used to produce steam at lower cost than any of the fossil fuels available
at today’s prices; and (4) air pollution can be reduced to the level required by
federal, state and local laws through the use of wet scrubbers or electrostatic
precipitators, usually more economically than in individual plants which are
replaced. In addition, front-end recovery of certain material resources such
as aluminum, copper, steel, etc., may be realized if the secondary materials
markets warrant. The reclaim value of some of the materials in our solid waste
varies significantly. Situations have developed in which the cost of separation
has been greater than the sales value.
The calorific energy resource continues to increase in value and is one of the
solid waste ‘“‘components”’ for which there is a profitable and growing market.
The heat energy may be extracted from ‘“‘solid waste fuel’’ in several different
forms: (1) shredded to produce “‘fluff’’, (2) pelletized, (8) gas, and (4) liquid
or incinerated to produce steam for process use, etc. This analysis will
evaluate the market for the heat energy when extracted in a conventional
incineration process to produce steam for use in cooling, heating, or certain
process requirements.
There are several markets or uses for the recovered heat. As examples:
(1) Process needs in manufacturing facilities.
(2) Industrial parks in which process and/or factory comfort cooling or
heating is required.
(3) Metropolitan urban or commercial areas where new as well as existing
offices, stores, banks, hotels, etc., require year-round climate control.
(4) College and university campuses with existing central heating and
cooling plants serving academic, dormitory, administration, student union,
library and other areas on campus.
(5) Medical centers with diverse usage such as laboratory, research, surgery,
patient and administrative areas.
(6) Airport complexes where central heating and cooling facilities provide
environmental control for each building.
(7) Shopping centers where sales areas, malls and miscellaneous spaces
are supplied with coolant and medium-temperature water for control of
temperature and humidity.
(8) Apartment complexes with several high-rise facilities as part of an urban
development program. |
(9) Power generation where solid waste heat energy may serve as supplement |
to the prime energy for base load or peak shaving usage. |
Kach of these applications or markets requires a different amount of coolant |
and heat per unit of demand. In other words, each will have a different load
factor. Reference to “load factor”’ throughout this paper refers to the ratio
of yearly unit sales or usage to the yearly production.
Potential yearly production must allow for the scheduled and unscheduled
outages of the incineration equipment. Expressed more succinctly, load factor
is the steam sales and/or equivalent metric ton-hours per year divided by steam
produced. In-plant usage, line losses and miscellaneous losses therefore are
excluded.
The load factor range for each of these applications as derived from ASHRAE
studies is shown on Table 1. Specifically, a manufacturing process which re-
quires a fixed quantity of steam each operating hour will have the highest
load factor of any of the markets analyzed. The demand is affected solely by
the production process. It is not dependent upon the weather or outside
conditions which affect transmission and ventilation air heating.
TABLE 1
Load factors
Applications (markets )
(1) Manufacturing facility
(process use only) 0.70—0.80
(2) Industrial park
(heating only ) 0.25—0.35
(heating and cooling) 0.50—0.60
(3) Metro urban area
(heating and cooling) 0.60—0.70
(4) University campus
(heating and cooling) 0.40—0.50
(5) Medical center
(heating and cooling) 0.47—0.57
(6) Airport complex
(heating and cooling) 0.55—0.65
(7) Shopping center
(heating and cooling) 0.85—0.45
(8) Apartment complex
(heating and cooling) 0.37—0.47
The second market of Table 1 has one condition — that when only building
heating is required, the consumption will be minimal. If heating and cooling
of the facilities in an industrial park are provided, this year-round need for
steam improves the load factor. However, the consumption in spring and fall
is quite low. During these periods, excess steam is condensed unless another
use is available.
The remainder of the markets listed in Table 1 in which the cooling and
heating needs are influenced primarily by the weather all have substantially
:
200 |
|
the same seasonal demands and yearly load factor. In some instances the t
internal feature of the cooling load has a noticeable impact on the consumption. |
The load factor has a significant impact on production cost, since it affects }
the revenue available from either steam, medium- or high-temperature water, |
or coolant. It is axiomatic that the higher the load factor the lower the pro-
duction cost; therefore, applications such as manufacturing with a daily and
year-round demand for heat energy will have the lowest production cost.
Initial investment for a solid waste incinerator facility with heat recovery
and pollution control equipment will be affected by several different factors;
specifically:
(1) Plant capacity.
(2) Type of pollution control equipment.
(3) Type of solid waste preparation and handling system.
(4) Type and quality of heat energy produced together with type of fluid
used for transfer from plant to point of usage.
(5) Area of country (i.e., Northeast, Southeast, West, etc.).
Some of these data may be incorporated in curves such as shown in Fig. 1.
From previous studies the data developed have been collected and interrelated
for budget cost estimates for a typical incinerator design. These curves apply
only to the Southeast area of the United States. Specifically, the heat recovery
equipment consisting of water wall furnace, main heat exchanger, superheater
and economizer section. A moving grate assembly, which provides “‘turnover”’
and mixing to obtain more complete combustion, would also be incorporated
in the overall design and operation of the incinerator.
The building is of standard industrial type construction with solid waste
storage pits sized for at least three full days of operation. Also included are
auxiliary oil burners and forced and induced draft fan assemblies. The stack
gas pollution control equipment is for both particulate and gaseous pollutants.
The piping, wiring, controls, on-site labor, and site preparation are included
in the budget curve. Also included are fees for financing, design, legal work,
and cost of money during the constructing period. These items are shown
under A in the figure.
When initial investment for the basic plant has been determined from
Fig. 1 and distribution system(s) type and length have been established, these
budget costs may be added to the basic plant cost and a total or new budget
cost per metric ton determined. This new cost may be used to calculate fixed charges
The distribution system(s) costs will vary depending on the type of fluid;
namely, steam or hot water and chilled water for service to an industrial park,
medical center, airport, urban development, etc. Assuming a representative
length for the distribution (namely, comparatively short run for only steam
to a manufacturing plant and an extensive “‘finger’’type distribution system
for the two commodities to serve an urban development project), the types
of piping and insulation excavation, filling, and resurfacing as required, a
budget cost for this portion of the project can be established and then added
to the base costs obtained from Fig. 1 to obtain a complete financial analysis.
j
201
>
Lo)
a |
INITIAL INVESTMENT ($ x103/ DAILY. TONNE ) i
o (00) Co) oO = pe)
OWNING & OPERATING COST ($/IOOOKG STEAM)
——————— eee eee eH
NMYNO WoO aw bp
BO MON SF, © Of
>
i | STEAM (MKG/HR. DEMAND) 7
00 400 600 800 1000 1200 1400 1600 1800
200 00 1000 =. 1200 1400
400 600 8
SIZE (DAILY TONNES DEMAND)
Fig. 1. Budget cost for incinerators applicable to southeast area U.S. and
adjusted to 1975 level. (A) Initial investment includes incinerator unit with waste heat
recovery, pollution control equipment, stack and breeching, building with solid waste
storage, piping, wiring, controls, charging system, on site labor, fees, supplementary fuel
facilities, financing cost during construction. (B) Owning and operating cost includes
fixed charges based on 20 year depreciation, 7% interest, taxes, insurance, operating
personnel, electricity, supplementary fuel, water, chemicals, routine maintenance, service
contracts and with yearly load factor = 0.50.
“Based on 2500 kcal/kg solid waste 65% conversion efficiency.
The incremental costs for the distribution system and complementary
changes in the incineration plant are shown in Table 2.
The cost additions are expressed as multipliers on the base cost of a con-
ventional incinerator plant. As an example, to provide 150 psi (1.03X 10° Pa)
steam to a manufacturer as shown by line A-2, base cost will be increased by
6 percent. This presumes a close coupled arrangement with plant on the
manufacturing site and the steam and condensate routed for minimum inter-
ference.
Should both coolant and steam be provided to several manufacturers in
an industrial park as shown by line B-2, the base cost will increase 56 percent.
202
TABLE 2
Initial investment multiplier (for use with Fig. 1 curve A)
Invest. multiplier
(A) Manufacturing (process use only )
(a-1) Steam at 15 p.s.i. (1.05 kg/cm? ) 1.080
(a-2) Steam at 150 p.s.i. (10.55 kg/cm? ) 1.060
(a-3) Steam at 265 p.s.i. (18.6 kg/cm? )
and 38°C superheat 1.050
(a-4) Steam at 400 p.s.i. (28.1 kg/cm? )
and 66°C superheat 1.045
(B) Industrial park
(b-1) Steam at 150 p.s.i. (10.55 kg/cm? ) 1.060
(b-2) Steam at 150 p.s.i. (10.55 kg/cm? ) 1.560
(C) Metro urban complex
(c-1) Steam at 150 p.s.i. (10.55 kg/cm? )
coolant at 5°C 2.050
(c-2) Water at 143°C, coolant at 5°C 2.000
(D) University campus
(d-1) Water at 143°C, coolant at 5°C 224.0
(d-2) Steam at 150 p.s.i. (10.55 kg/cm? )
coolant at 5°C 2.260
(E) Medical center
(e-1) Steam at 150 p.s.i. (10.55 kg/cm? )
coolant at 5°C PASLFED)
(F) Airport complex
(f-1) Water at 143°C, coolant at 5°C 2130
(G) Shopping center
(g-1) Water at 143°C, coolant at 5°C 2.120
(H) Apartment complex
(h-1) Water at 143°C, coolant at 5°C 2.100
In this instance, a chilling plant is required and the facility will be located on
the complex. Two distribution systems with laterals are required, hence
approximately a 50-percent increase over the basic cost.
The metro urban complex, (market C), university campus (market D) and
the remaining markets analyzed require heating either in the form of medium-
temperature water or steam and coolant at about 5°C.
The increase in initial investment over that for the base plant is about 100
percent. This includes the chilling plant with auxiliaries such as heat rejection
equipment, low head and primary pumping equipment, piping, service valves,
etc., and building. The incinerator facility would be remote and the services
may be in the street, therefore an additional premium for the distribution
systems would be added.
The data gathered from various feasibility studies prepared during the past
several years have served as a basis for the design and description of the solid
waste facility referred to in the preceding paragraphs. Total initial investment,
:
|
|
|
203
thus determined, can be used for budgeting purposes. Also, fixed charges may
be readily calculated. Included, however in Fig. 1, curve B, are owning and
operating cost data for the basic plant when operated at a load factor of 0.50.
Bases for depreciation, value of money, etc., are indicated.
The owning and operating cost correction factors used for the different type
distribution systems and plant modifications for the different applications
are shown in Table 3. This multiplier, when used with curve B, will provide
for budgetary purposes the cost of steam production when the plant load
factor is 0.50. As an example, assume owning and operating costs for an in-
cinerator plant serving a metro urban complex are required. This figure must
include increased fixed charges for plant modification and for the distribution
systems over and above those indicated by curve B. With load factor of 0.50
and with steam at 150 p.s.i. (1.03X 10° Pa) for heating and coolant at 5°C for
cooling and dehumidifying, the multiplier for ‘“‘C-1”’ is 1.714 — in other words,
71.4 percent more than indicated by curve B. This presumes the load factor
is 0.50. .
TABLE 3
Owning and operating cost multiplier (for use with Fig. 1 curve B)
Fixed charge
multiplier
(A) Manufacturing (process use only )
(a-1) Steam at 15 p.s.i. (1.05 kg/cm? ) 1.055
(a-2) Steam at 150 p.s.i. (10.55 kg/cm? ) 1.041
(a-3) Steam at 265 p.s.i. (18.6 kg/cm? )
and 38°C superheat 1.034
(a-4) Steam at 400 p.s.i. (28.1 kg/cm? )
and 66°C superheat 1.034
(B) Industrial park
(b-1) Steam at 150 p.s.i. (10.55 kg/cm? ) 1.041
(b-2) Steam at 150 p.s.i. (10.55 kg/cm? )
coolant at 5°C 1381
(C) Metro urban complex
(c-1) Steam at 150 p.s.i. (10.55 kg/cm? )
coolant at 5°C Wii
(c-2) Water at 143°C, coolant at 5°C 1.680
(D) University campus
(d-1) Water at 143°C, coolant at 5°C 1.823
(d-2) Steam at 150 p.s.i. (10.55 kg/cm? )
coolant at 5°C 1.857
(E) Medical center
(e-1) Steam at 150 p.s.i. (10.55 kg/cm? )
coolant at 5°C 1.796
(F) Airport complex
(f-1) Water at 143°C, coolant at 5°C 1.768
(G) Shopping center
(g-1) Water at 143°C, coolant at 5°C 1.762
(H) Apartment complex
(h-1) Water at 143°C, coolant at 5°C 1.748
204
Table 1 indicates the load factor range for different applications. Corrected
production costs due to deviation from the base load factor of 0.50 to that
applicable to the application under consideration may be obtained from Table
4. For a metro urban complex C a multiplier of 0.843 is used to correct from
0.50, the basic load factor used for curve B in Figure 1, to 0.65, the average
for such applications. The net correction, therefore, is 1.714X 0.843 = 1.445.
Subsequent calculation will amplify on this correction procedure. These multi-
pliers take into account the relative impact of owning as well as all operating
costs.
TABLE 4
Load factor multiplier (for use with Fig. 1)
Application (market) Load factor
multiplier
(A) Manufacturing (process use only ) 0.816
(B) Industrial park
(heating only) 1.445
(heating and cooling) 0.936
(C) Metro urban complex 0.843
(D) University complex 1.081
(E) Medical center : 0.976
(F) Airport complex 0.883
(G) Shopping center 1.187
(H) Apartment complex 1.141
Generally speaking, the fixed charges for the incinerator facility with heat
recovery, proper pollution control for both gas and liquid effluent, chilling
plant, distribution system, etc., will be approximately 65 to 68 percent of
the overall owning and operating costs. Of the remaining 32 to 35 percent,
about 18 to 20 percent of owning and operating costs (that is, 55 percent of
operating costs) is independent of plant output. This segment of costs includes
operating personnel management, and general administrative expense. Other
operating costs such as electricity, water, chemicals, supplementary fuel, and
routine maintenance and service vary with steam production. This segment is
approximately 45 percent of operating costs or about 15 percent of owning
and operating expenses. As a result, the higher the load factor and yearly pro-
duction, the lower the production costs. Expressed in another manner, if the
system load factor were increased from the base factor of 0.50 to 0.60 (an
increase of 20 percent), the total costs would increase only about 3 percent.
In addition, if there were a 20-percent increase in gross income with only a
3-percent increase in owning and operating costs, the unit selling prices could
be reduced if it were a “not-for-profit” operation or the profit picture would
be enhanced if a profit-making corporation.
205
As an example of the foregoing, assume that budget costs are required for
(1) initial investment; (2) fixed charges; (3) owning and operating costs; and
(4) production costs for a 1,000 ton per day (907 metric ton) solid waste
capacity plant with chilling plant sized for a heating to cooling demand ratio
of 1.0 and serving an urban area with new and existing offices, stores, banks,
hotels, etc.
Table 1 indicates that the load factor for metro urban areas will vary be-
tween 0.60 and 0.70. This information will be used later.
Figure 1, curve A, indicates that initial investment for a 1,000 ton per day
(907 metric ton) basic plant is $ 8,000 per ton ($ 8,820 per metric ton) or
$ 8,000,000. Included in this figure are costs as listed in Fig. 1, item A.
Table 2 shows the multiplier for addition of distribution system and chilling
plant. For application to market C, “‘metro urban complex” (using steam at
150 psi [1.03X 10° Pa] for heating and 5°C coolant), the indicated correction
factor is 2.050. The revised investment figure is $ 8,000,000 X 2.05 =
$ 16,400,000. |
Fig. 1, curve B, indicates the overall owning and operating costs for a base
plant when operated at a load factor of 0.50. From curve B, the owning and
operating costs or production costs are $ 1.79 per 1,000 kilograms of steam.
Table 3 shows adjustment in owning and operating costs (production costs)
because of the additional expense of distribution system and chilling plant.
This correction multiplier for C (metro urban complex), with steam for heating
and water for the coolant is 1.714; therefore, production cost is $ 1.79 X 1.714
= $ 3.07 per 1,000 kilograms of steam. This is the cost if the load factor were
0.50.
Table 4 shows the correction due to the metro urban complex load factor of
0.60—0.70 (use 0.65) instead of the 0.50 which is the basis for curve B in
Figure 1. This correction factor is 0.843. Therefore, production costs are
$ 3.07 X 0.843 = $ 2.59 per 1,000 kilograms of steam.
The result of the above exercise is:
(1) In-place cost for plant with distribution system is $ 16,400,000.
(2) Production cost for services to the metro urban complex having a load
factor of 0.65 is $ 2.59 per 1,000 kilograms of steam.
Information such as this may be used during the preliminary stages of
discussion and before the feasibility study is complete.
Should there be interest in return on investment at this preliminary stage,
it is approximately 5 percent based on sales at $ 3.86 per 1,000 kilograms of
steam, initial investment of $ 16,400,00 per metric ton capacity, and conversion
efficiencies which provide 2,470 kilograms of steam per metric ton (103
kilograms of steam per hour per metric ton of waste). However, if the munici-
pality pays a nominal amount for incineration in lieu of landfill (namely, $ 2.72
per metric ton), the return on investment will be approximately 11 percent.
In time, economical techniques for recycling of certain components and
markets should develop which will provide additional income. Supplementary
income for paving base or building block can be obtained from the residue
after separation.
206
In conclusion, there will be an ever-increasing amount of solid waste. Dis-
posal will surely utilize the most economical techniques consistent with the
air, water, and land pollution constraints. Conventional incineration and
pyrolysis — processes in which the energy may be recovered and put to an
economical and useful purpose — are disposal methods which appear to have
merit.
Engineers are frequently called upon to evaluate the economics of the many
different disposal methods for our ever-increasing amounts of solid waste.
After a comprehensive study, they can recommend to the municipality the
best solution to the disposal problem. Some sections of our country do not
have sufficient amounts of certain low-cost convenience fossil fuels to serve
the needs of all industries in their area. The heat energy in our solid waste may
be a partial answer to this problem. |
This study may be helpful in analyzing problems and provide preliminary
information for budgeting purposes. The data could be used for preliminary
discussion prior to a more comprehensive study.
Resource Recovery and Conservation, 1 (1976) 207—216 207
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
ENERGY AND RESOURCE RECOVERY FROM SOLID WASTES*
G.M. MALLAN and E.I. TITLOW
Occidental Research Corporation, La Verne, Calif. 91750 (U.S.A.)
(Received 19th March 1975)
INTRODUCTION
In 1969, long before the present awareness of energy shortages and depleted
resources, the Occidental Research Corp. (formerly Garrett Research and
Development Company, Inc.), a subsidiary of Occidental Petroleum Corpo-
ration, set out to develop a process that would recover oil and other resources
from municipal refuse. A basic decision was made initially — the object of
the research was not to produce the least cost waste disposal system, but
rather to produce grades of recovered material which could find a ready and
high value market. The results of this research and marketing are summarized
here.
PROCESS DESCRIPTION
A simplified flow diagram of the Occidental Energy and Resource Re-
covery process is shown in Fig.1 and incorporates the following operations:
(1) Primary shredding of the raw refuse to smaller than 7.6 cm (3 in.).
(2) Magnetic separation of ferrous metals.
(3) Air classification to remove most of the inorganic material from the
pyrolysis feed.
(4) Drying of the shredded refuse to about 3 percent moisture.
(5) Screening of the dry material to reduce the content of free inorganic
material to below 4 percent by weight.
(6) Recovery of aluminum, and a clean glass product.
(7) Secondary shredding of the organic material to pieces smaller than
1.168 mm (14 mesh).
(8) Flash pyrolysis of the organics.
(9) Collection of the pyrolytic products under rigid pollution control con-
ditions.
All of these operations, except primary shredding which was conducted
under contract elsewhere, were studied in detail, both individually and in
various combinations. They may be grouped and evaluated as two distinct
*Paper presented at the Symposium “‘Energy Recovery from Solid Waste”, March 13—14,
1975.
208
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209
subsystems — feed preparation, including recovery of metals and glass; and
pyrolysis, including the recovery of salable fuels.
Feed preparation. The primary purpose of the feed preparation subsystem is
to deliver dry, finely divided, essentially inorganic-free feed material to the
pyrolysis reactor. An important secondary purpose is to allow the economic
recovery of magnetic metals, aluminum and clean glass. During investigations
of this subsystem, several combinations of the various unit operations were
evaluated in order to develop the most efficient process with respect to product
quality and operating costs.
One of the more important functions of the feed preparation subsystem
is to minimize the content of the inorganic materials in the pyrolysis feed
material. While the pyrolysis process itself is virtually unaffected by the in-
organics, these materials degrade the quality of the residual char and in-
crease maintenance costs for secondary shredding. During the early phases
of the pilot plant program, it was thought that the free inorganic content
of primary shredded wastes could be reduced to less than 4 percent by merely
drying the refuse before air classification; however, it was determined that
air classification must precede the drying step and air classifiers are now a
standard item in the process chain.
Separating ferrous metals from refuse is relatively simple and is done mag-
netically. This is a well established process. However, it was found that re-
covery of glass and aluminum required development of entirely new tech-
niques.
Glass recovery process. The glass recovery process developed uses froth flo-
tation (a process well-known in minerals beneficiation). An innovation was
a new selective chemical reagent to cause the previously classified and ground
glass to attach itself to the air bubbles generated in a froth flotation cell,
leaving non-glass impurities behind. The process is shown schematically in
Fig.2. About 70 percent of the glass contained in the as-received refuse can
be recovered as a 99.7 percent pure product which, we have found, can com-
mand a good price in the glass container manufacturing market.
Aluminum recovery (““RECYC-AL’’). In mid-1972, an assessment of non-
ferrous metal recovery technology was made as part of our resource recovery
effort. At that time, heavy media separation, and screening or hand sorting
seemed to be the only processes under active investigation for treating muni-
cipal refuse. Upon consideration of markets for scrap aluminum, it became
obvious that secondary metal processors would pay a high price for recovered
metal only if it meets rather rigid specifications. Occidental thus decided
upon a dry separation process using linear induction motors (LIM) to recover
selectively electrically conductive metals from the shredded, air classified
refuse.
210
OVERHEAD TO PYROLYSIS
MUNICIPAL
REFUSE
rr
PRIMARY :
SHREDDED
a.
——> + |.9cm(3/4") METALS, ORGANICS
CLASSIFIER =| - 71 +0.074mm
(-24 + 200 MESH)
FLOTATION
CELLS
=H
INORGANIC REJECTS
-0.074mm
(-200 MESH)
TO WASTE
PRODUCT GLASS
(99.7% PURE)
Fig.2. Occidental glass recovery process.
In the Occidental RECYC-AL process, shown schematically in Fig.3, one
or more LIMs are positioned just beneath a non-conductive conveyor belt
which is driven by a variable speed drive. Refuse that has been previously
air classified and processed to remove magnetic metals is fed from a hopper
onto the conveyor belt. The linear induction motors operate on an alter-
nating current, variable-frequency power source. As the refuse containing
aluminum passes over the LIM, eddy currents are induced in the pieces of
aluminum, producing a magnetic field of opposite polarity to that field pro-
duced by the LIM. Because magnetic fields of the same polarity will repel
each other, the resulting magnetic force causes the aluminum pieces to
change direction rapidly toward the edge of the conveyor belt. A baffle
positioned at the edge of the belt traps the aluminum, which then flows to
LINEAR MOTORS
/ VIBRATING
OSCILLATING
FEEDER
NONCONDUCTIVE CONVEYOR
1.82 METERS
(6 FEET)
3.04 METERS
(lO FEET)
COLLECTION BIN
Fig.3. Occidental “‘RECYC-AL” aluminum separator process.
211
a product bin. The remaining refuse, which is essentially free of glass and
metals, is then recycled back into the process. Nearly 60 percent of the
aluminum present in the as-received refuse was recovered in experimental
trials. The capacity of the pilot machine developed to date is 1.8 to 3.6 t
(2 to 4 U.S. tons) per hour, of air-classified, screened rubbish usually con-
taining from 7 to 20 percent aluminum. The particle size of the metal that
can be recovered can be as small as 2.5 cm (1 in.) in the longest direction.
Secondary shredding. The heart of the Occidental feed preparation subsystem
lies in the secondary shredding operation. A finely divided organic feed to
the pyrolysis reactor is desirable if high oil yields at atmospheric pressure
are to be achieved. Extensive vendor testing was conducted on five different
units before a 40 hp, 454 kg (1000 pound per hour) hammer mill was in-
stalled for the pilot plant program. Prolonged testing over many months has
shown that power requirements and maintenance costs using dry, essentially
inorganic-free material from municipal refuse will result in acceptable oper-
ating costs.
Pyrolysis process. The Occidental pyrolysis process involves the rapid heating
of finely shredded organic materials in the absence of air using a proprietary
heat-exchange system. This technique was developed to maximize liquid fuel
yields, thus generating the maximum income per ton of wastes. There are a
number of solid waste pyrolysis processes under development today which
maximize gas yields rather than liquids. However, pyrolysis of cellulosic feed
stocks at gasification temperatures is usually endothermic by about 1400 to
1860 J/g (600 to 800 Btu/lb.), while the same reaction at 480°C (900°F) is
slightly exothermic. Liquefaction is thus a more efficient conversion process
and it also produces a more easily stored product which can be sold on the
basis of its heating value.
During laboratory pyrolysis studies using a small continuous 2.26 kg (5 |b.)
per hour reactor, oil yields of about 40 weight percent were obtained with
dried municipal wastes from which about 90 percent of the inorganic mate-
rial had been removed. These oil yields have now been confirmed on a larger
scale using 3,628 kg (4 ton) per day pilot plant. Pyrolysis of cellulosic mate-
rials also produces a residual char, combustible gases, as well as by-product
water. The distribution of these products has a significant effect upon the
economics of the overall process. The gas produced under optimum lique-
faction conditions has a moderate heating value of about 18.6 X 10° J/m°
(500 Btu/ft?) at the outlet of the reactor. This fuel is burned on-site for
process heat and a portion of the char is also used for the same purpose.
212
DESCRIPTION OF RECOVERED PRODUCTS
Perhaps the most important aspect of any resource recovery system is the
quality of the products to be returned to the economy. A great deal of nega-
tive comment has been generated during the past few years about the lack of
suitable markets for recycled materials. In reality, the problem is not so much
the markets but the quality of the recovered products. Magnetic metals
heavily contaminated with organic material and non-ferrous metals will not
find ready outlets, nor will any other contaminated commodity. A consider-
able amount of effort was thus spent on upgrading the quality of recovered
materials.
Glass
The effort to produce high purity recycled products from municipal re-
fuse is most graphically illustrated by the glass recovery process described
earlier. More than 70 percent of the glass contained in packer truck waste
can be recovered as a sand-sized, mixed-color product of greater than 99.7
percent purity. About two-thirds of the remaining impurities are carbonaceous,
and these present little or no problem upon remelting for the manufacture
of new containers. |
Laboratory melt studies conducted by Owens-Illinois on sample cruets
made from 100 percent recovered glass from the Occidental process have
shown none of the normal imperfections often found in reclaimed glass.
These imperfections are cords, stones, blisters or seeds, and none could be
found at 10—power magnification.
Aluminum
Although the “‘separating”’ action of the RECYC-AL machine affects all
conducting materials, there are considerable differences among various metals
and configurations. It has been found that the RECYC-AL process minimizes
the occurrence of such undesirable materials as stainless steel, lead and bismuth |
in the product stream. Because of the extreme qualitative variability in com- |
position of the input of municipal waste, it is difficult to produce a
standardized product. However, in experimental trials the RECYC-AL pro-
cess has been found to reduce greatly the incidence of undesirable compo-
nents in the product metal. At this stage in its development the process is
not expected to produce aluminum consisting almost entirely of aluminum
cans, but the product metal is expected to be composed of more than 90
percent by weight aluminum with small quantities of contaminant.
Markets for the recovered aluminum have been determined throughout
the U.S. and many secondary metal processors are willing to make long term
purchase commitments because of the consistent quality of the product
that can be attained.
213
Pyrolytic oil
The Occidental system employs a pyrolysis process which converts the or-
ganic portion of municipal waste to usable synthetic fuel oil. The pyrolytic
oil is, in fact, the single most important product obtained. As might be ex-
pected from its genesis, pyrolytic oil differs in many important respects
from fuel oil derived from petroleum. The synthetic product is a highly
complex, oxygenated, organic fluid rather than a hydrocarbon. The sulfur
content is from 0.1 to 0.2 percent by weight, far lower than most petroleum
based fuel oils. Because it is lower in both carbon and hydrogen than the
latter, the average calorific value of the synthetic oil is about 24400 J/g
(10,500 Btu/lb.) compared to 42,300 J/g (18,200 Btu/lb.) for a typical resi-
dual oil. However, since the densities of pyrolytic oil and typical No. 6 are
1.30 and 0.98 respectively, the fuel oils are generally sold by volume rather
than by weight; a comparison of heating values is much more favorable to
pyrolytic oil when expressed on a volumetric basis. Oil derived from the
pyrolysis of municipal waste contains some 76 percent of the heat energy
available from No. 6 oil.
It has been observed that pyrolytic oil is a good deal more viscous than a
typical residual oil. This means, of course, that it must be stored, pumped
and atomized at somewhat higher temperatures. Combustion tests with some
870 liters (230 gallons) of oil at the research facilities of a large manufacturer
of power plant equipment have shown that the pyrolytic oil could be pumped
without trouble at 71°C (160° F), and that satisfactory atomization was
achieved with 0.3 X 10° Pa (50 psi) steam when 37,85 liters (10 gallons) per
hour of oil was delivered to the burner tip at 0.2 X 10° Pa (25 psi) and 115°C
(240°F). Atomization with cold compressed air at 0.7 X 10° Pa (100 psi) re-
sulted in the formation of a much coarser droplet spray, and it is probable
that preheating would be needed.
It was also found that pyrolytic oil can be compatibly mixed with most
No.6 fuel oils. Laboratory tests have shown that equal quantities of each
can be blended together to produce a relatively easy-to-handle two-phase
mixture. This had not been anticipated. It was known that the heavier tar
fuels obtained from the carbonization of coal cannot be mixed with
petroleum oil fuels because of the precipitation of a gelatinous bituminous
material, and it was feared that pyrolytic oil might also exhibit the same be-
havior. Further studies are planned on the storage, handling and combustion
properties of blends of No.6 and pyrolytic oil. If further work confirms the
compatability of the two fuels, blends can be tailored to take advantage of ~
the superior properties of each. Thus, the high sulfur content of a residual
petroleum-based oil can be reduced by the low sulfur pyrolytic oil, which
in turn will have its viscosity lowered.
214
ECONOMICS OF THE OCCIDENTAL PROCESS
The Occidental pyrolysis process is designed as a flexible, pollution-free
system which requires relatively low capital costs per ton of installed capa-
city. However, since there are a number of distinct feed preparation opera-
tions required, the process will be fairly labor-intensive until a semi-auto-
mated system can be developed. For this reason, the economics of scale
currently have an appreciable effect upon operating costs. A summary of
the estimated economics for a 2,000 ton/day plant is shown in Table 1.
These operating costs include provision for a complete administrative staff
of 13 people, from plant manager to clerks and secretaries. The plant itself
will require nearly 60 operators for 24 hours per day, seven days per week
— this labor has been estimated at $50,000 per year, per shift-job.
TABLE 1
Estimated economics of 1,816 t/day (2,000 U.S. ton/day) solid waste pyrolysis plant
Total plant capital (excludes land) $ 32,800,000
Working capital 800,000
Annual op. cost (amortization, 20 yrs. at 6%) 11,600,000
Annual net revenue from sales 13,600,000
Annual profit : 2,000,000
Cost per ton (350 days per year) 16,57
Net revenue per ton (350 days per year) 19,44
Net profit per ton 2:87
In addition to these attractive economics, the Occidental process is also
thermodynamically efficient. The net thermal output of the plant, expressed
in electrical terms, is developed in Table 2.
TABLE 2
Overall energy balance of 1,816 t/day (2,000 U.S. ton/day) Occidental solid waste
pyrolysis process
Total energy in one ton as-received refuse” 10.548 GJ
~ (10 MM Btu)
Energy in 1.1 bbl of oil per ton refuse 5.569 GJ
(5.28 MM Btu)
or 1,547 kWh
At a power plant conversion efficiency of 34%
Recovered electric power per ton refuse 530 kWh
Consumed electric power per ton refuse 140 kWh
Net recovered electric power per ton refuse 390 kWh
7 Assumes 25% moisture
215
The pyrolysis process has been shown to be an attractive alternative for
recycling tires, tree bark, rice hulls, and other waste products in experimental
trials. Thus, the prospects for widespread utilization appear to be quite
promising.
SOLID FUEL AS A PRODUCT
This paper has described the Occidental Resource Recovery System that
produces, in addition to high grades of minerals, energy in the form of a
pyrolytic oil. To prove the technical viability of the flash pyrolysis process
on acommercial scale, a 181.5 t/day (200 U.S. ton/day) demonstration is
presently being built in San Diego County, California,with funding by the
Environmental Protection Agency. This technology will not be offered
commercially until this demonstration is successful. The “‘front end”’ of this
technology, however, is available with energy recovered as a dry fibrous solid
fuel.
Bridgeport, Connecticut
After many months of extremely complex negotiations, a contract has
recently been executed between the Connecticut Resources Recovery
Authority and Occidental. Under the terms of this contract, Occidental will
design, build and operate a 1,360 t (1,500 U.S. ton) per day facility in
Bridgeport to serve a large part of Southwestern Connecticut. Virtually all
of the municipal waste from the specified area will be disposed of by the
Occidental plant and its associated transfer stations under a 22% year
contract. In addition to the innovative technology that will be used, the
contract is a novel and remarkable example of successful cooperation be-
tween the public and private sectors.
Dry, fibrous fuel. The Occidental Resource Recovery System that will be in-
stalled in Bridgeport is schematically identical with the process described in
the paper up to the stage of secondary shredding. In the Bridgeport process
TABLE 3
Estimated economics of 1,816 t/day (2,000 U.S. ton/day) resource recovery plant
(solid fuel)
Total plant capital (excluding land) $26,000,000
Working capital 650,000
Annual operating cost (amortization, 20 yrs at 6%) 9,500,000
Annual net revenue from sales [fuel at $1.00/1.054 GJ ($1.00/MM Btu) ] 9,750,000
Annual profit ~ 250,000
Cost/ton (350 days/yr.) 13.57
Net revenue/ton (350 days/yr. ) 13.93
Net revenue/ton — 0.36
216
line, the secondary shredder reduces the material only to a nominal 1.2 cm
(44 in.) size, and the material will be then sent to a local utility for burning
in conjunction with heavy oil. This fuel can be utilized only in boilers
equipped with ash handling and “back end”’ cleaning equipment, or perhaps
in cement kilns.
The economics of a full line resource recovery plant that will produce such
a solid fuel are given in Table 3. 7
BIBLIOGRAPHY
1 Morey, B.T., 1974. Inorganic resource and solid fuel preparation from municipal trash.
In E.E. Aleshin (Ed.), Proc. Fourth Mineral Waste Utilization Symp., Bu. Mines and IIT
Res. Inst., Chicago, pp. 85—94.
2 Bauer, H.F., 1975. Preliminary Hydrogenation of Pyrolytic Oil from Municipal Refuse,
March, Occidental Research Corp.
3 Morey, B.T., Griffin, T.D. and Cummings, J.P., 1975. Recovery of small metal particles
from nonmetals using an eddy current separator — Experience at Franklin, Ohio. In:
Proceedings, 104th Annual Meeting, American Institute of Mining Metallurgical and
Petroleum Engineers, New York City, Feb. 16—20.
4 Morey, B.T. and Rudy, S., 1975. Aluminum recovery from municipal trash by linear
induction motors. In: Proceedings, 78th National Meeting, American Institute of
Chemical Engineers, Salt Lake City, Utah, Aug. 18—21.
5 Morey, B.T. and Cummings, J.P., 1972. Glass recovery from municipal trash by froth
flotation. In M.A. Schwartz (Ed.), Proc. Third Mineral Waste Utilization Symp., Bu.
Mines and IIT Res. Inst., Chicago, pp. 311—322..
6 Bauer, H.F., 1974. Corrosion Studies of Pyrolytic Oil from Solid Waste. Aug., Occi-
dental Research Corp. :
Resource Recovery and Conservation, 1 (1976) 217—224
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
FEASIBILITY STUDY FOR BURNING REFUSE-DERIVED FUEL IN THE
DISTRICT OF COLUMBIA BY POTOMAC ELECTRIC POWER COMPANY*
B. VINCENT VISCOMI**
Lafayette College, Easton, Pa. 18042 (U.S.A.)
(Received 19th March 1975)
ABSTRACT
This paper describes a study conducted to determine the economic feasibility of a
project for producing and burning refuse-derived fuel RDF in the District of Columbia.
Alternate modes of processing,transporting, handling and burning RDF were considered.
The study concluded that it is economically feasible to implement the project and
identifies the most cost-effective approach for utilization of existing capital facilities. The
study can possibly serve as a model for implementation of this form of energy recovery
elsewhere.
INTRODUCTION
In May of 1974, a task force committee, consisting of representatives of
the District of Columbia’s Department of Environmental Services (DES), the
Potomac Electric Power Company (PEPCO) and the National Center for
Resource Recovery, Inc. (NCRR) was established to investigate the feasibility
of a refuse energy recovery project in the District of Columbia. Specifically,
the study was to consider the economic and design alternatives involved in
the preparation of RDF at the DES Solid Waste Reduction Center Number 1
(SW RC-1), transportation to the adjoining PEPCO Benning Generating Station
and firing of RDF in one of the boilers.
The District of Columbia generates in excess of 635,000 tons of solid waste
annually. This refuse is collected by three classes of collectors; the District’s
Department of Environmental Services, the Federal Government, and by private
commercial collectors. The collected refuse is disposed of by one of three
methods: direct disposal at landfills operated by DES; delivery to one of three
DKS transfer stations, and after reloading, disposal at the landfill sites; and
incineration of solid wastes followed by disposal of residues by landfill. The
District presently operates three landfill sites, three transfer stations and one
incinerator.
The Potomac Electric Power Company is an investor-owned utility serving
449,000 customers in a service area of 1.7 X 10? m? including Washington
. Paper presented at the Symposium ‘“‘Energy Recovery from Solid Waste’’, March 13—14,
197.5:
a Faculty Participation Research Fellow, National Science Foundation, Summer, 1974,
at the National Center for Resource Recovery, Inc.
218
D.C., a portion of suburban Montgomery and Prince Georges Counties in
Maryland and a small commercial area in Arlington County, Virginia. PEPCO’s
current generating capacity is from fossil-fueled facilities; however, two
1100-MW nuclear plants are scheduled to be added to the system.
The Benning Generating Station is located on a 186,000 m? site on the east
bank of the Anocostia River in the District of Columbia and has seven gener-
ating units with a total capability of 751MW. Solid Waste Reduction Center
Number 1 is located adjacent to the Benning Station and consists of six
refractory-type refuse burning furnaces with a total capacity of 1500 tons/day.
Incorporated in the design of SWRC-1 is a shredding facility and magnetic
separator to shred oversize bulky waste prior to burning in the incinerator
furnaces.
In March, 1974, NCRR entered into an agreement with DES to conduct a
resource recovery test and demonstration program at SWRC-1. The resource
recovery system utilizes the large (1000 hp = 746 KW) shredder, a suitable air
classifier, and other equipment. For the NCRR program, the shredder is
operated on household and commercial refuse. Considering the close proximity
of the Benning Station and SWRC-1, it should surprise no one that, in a short
period of time, a task force to study energy recovery was underway.
PROJECT CONSIDERATIONS
The project, as envisioned by the task force at its inception, was to consist
of two, or possibly three phases. Each phase would be concerned with the
evaluation of alternative modes of processing, transporting, handling and
burning refuse-derived fuel. The primary purpose of the project, if implemented, |
was to develop firsthand information and experience in the following areas:
(1) processing of solid waste and production of RDF at SWRC-1 by DES,
(2) transportation of RDF by DES to Benning Station on a mutually
agreeable schedule, and
(3) feeding and firing of RDF as supplemental fuel in a Benning Station
boiler by PEPCO (Boiler No. 26 was selected on the basis of size and its
capability for both oil and coal firing).
The benefits accruing to PEPCO and DES would include information and
experience useful in determining the relative economics and benefits of the
process, the evaluation of potential technical problems, and the development
of new working relationships between the parties. All of the above would
contribute to the determination of this form of resource recovery to DES as
a significant means of disposal of solid waste and to PEPCO as a significant
supply of an economical supplemental fuel. |
Originally, the studies were to concentrate on achieving the project |
objectives at minimum cost and modification of existing facilities. For example,
early in the study some of the possible RDF firing techniques which were 1
considered included injection of RDF into the bunker, or the pulverizer, or the |
existing distribution piping. Subsequent investigations and conversations with |
|
!
|
i
\
219
equipment suppliers indicated that injection into a separate distribution system
is preferred. Many technical ideas were pursued; most were abandoned early
in their life. The final result was a detailed consideration of a two-phase program
with several technical alternatives as described below.
Under both phases, RDF would be produced at SWRC-1 by primary and
secondary shredding to a nominal particle size of less than 4 cm. Under Phase
I, the RDF would be transported by DES to a receiving facility at Benning
Station. DES would be responsible for the unloading of the vehicles and the
transfer of RDF to the PEPCO receiving bin. From the bin, PEPCO would be
responsible for pneumatically transporting the RDF to two corners of Boiler
No. 26. If two corner burning was found to be unacceptable, the system would
be modified to permit burning at four corners. Phase I includes testing, as
described later.
Phase II differs from Phase I only in that truck transport of RDF is replaced
by pneumatic conveying of the RDF directly from SWRC-1 to the PEPCO bin.
The testing and evaluation for each phase are outlined below:
Phase I
(1) For PEPCO:
a. Evaluate the RDF conveying and injection system as provided by
the equipment supplier to include erosion effects.
b. Perform fuel analyses of RDF as received.
c. Evaluate effect of RDF burning on boiler performance-efficiency,
slagging, corrosion, particulates, etc.
d. Determine impact of RDF burning on air pollution control equip-
ment and emissions.
e. Evaluate the effect of RDF burning on the bottom ash handling
system.
f. Determine operating and maintenance costs.
(2) For DES:
a. Modify existing equipment and install materials handling and
separation equipment at the SWRC-1 as necessary.
b. Determine operating and maintenance costs.
Phase II
(1) For PEPCO:
a. Continue Phase I program to identify and resolve problems asso-
ciated with RDF burning.
(2) For DES:
a. Install and evaluate pneumatic transport line to PEPCO receiving bin.
b. Develop design parameters and estimate capital and operating costs
for a continuous full-scale system.
220
SYSTEM ALTERNATIVES
For each phase, the task force considered various alternatives for delivering
RDF to Benning Boiler No. 26. In Phase I, four system alternatives were
studied and are described below (see Figs. 1—4).
Option A — This system involves the trucking of RDF to a location south of
SWRC-1 on DES property. The fuel would be loaded into a feed
hopper and conveyed to a bin on PEPCO property in the vicinity
of Boiler No. 28 cooling tower. From the discharge valve of the
bin, RDF would be pneumatically conveyed to Boiler No. 26.
Option B — This option replaces the long conveyor between the feed hopper
and bin of Option A with truck delivery to the bin located on
PEPCO property as described above. The remainder of the
system is unchanged.
Option C — This system involves the trucking of RDF to the east side of
Boiler No. 26 where the feed hopper and bin would be located.
This option reduces the length of the pneumatic conveyor of
options A and B but requires truck unloading operations in
this cramped and congested area.
Option D — For this option, RDF is trucked to the west side of Boiler No.
26. The PEPCO fence must be moved to accomodate a truck
and the feed hopper. The bin, also located on the west side of
Boiler No. 26, would be adjacent to the feed hopper but on
the PEPCO side of the fence. |
The equipment requirements common to all options, specific to each
alternative, and the advantages and disadvantages of each system were identified
and evaluated. Option D was selected as the Phase I system for detailed
analysis and further study. The primary reason for the selection of this option
is that it is the one of minimum interference with normal PEPCO operations —
it does not require an additional gate or guard and also does not require that
DES trucks enter PEPCO property. In addition, this option requires the
shortest lengths of pipe from the bin to the boiler and, hence, lowest installed
cost as compared to the other options.
For Phase II operations, the ideal location for the storage bin is the yard
area at the east side of the unit to provide the shortest pipe route from SWRC-1
to the bin. It is not anticipated that the bin would be moved to this location
after Phase I because the cost of moving, providing new foundations, and
rerouting the feed pipes to the boiler would exceed the cost of a few hundred
feet of additional pipe. However, if a decision should be made to bypass
Phase I and start with Phase II, consideration would be given to locating the
bin as mentioned above.
Costs for the installation and operation of equipment for the project were
estimated for DES and PEPCO in three categories: (a) general project costs,
(b) Phase I costs, and (c) Phase II costs.
7
>
5
224
——
| O SWRC NO.1 o |
TRUCK ROUTE —+»+ —» —>6§FEED HOPPER
COOLING TOWER
yt COOLING TOWER
re | SWITCHYARD
a Ke) = Pneumatic or belt
BLR.NO. 27 ie O conveyor
a Pneumatic ~~ J
== eee ay conveyor ne BIN
e BLR.
LR.NO. 2
a) 8 " ,
As) COAL bs
STORAGE
= Hate NO. 25 ee
O ey ena a,
a
OLD PLANT
: <a
im
—\ Zz
Fig. 1. Site plan of PEPCO Benning Generating Station indicating operational features
of option A.
RECOMMENDATIONS AND CONCLUSIONS
The task force committee concluded that it is economically feasible to
implement a pilot project for the production of RDF at SWRC-1 and its
utilization in Benning Boiler No. 26. The most cost-effective approach to this
project is to bypass the Phase I operations and to adopt the Phase II program.
The costs and benefits utilized to arrive at the above conclusion are based on
a facility processing 20 tons per hour of refuse and producing 14 tons per
hour of RDF for 12 hours per day and 260 days per year.
The task force recommendations are:
(1) PEPCO modify boiler No. 26 to burn RDF using a system recom-
mended by Combustion Engineering, Inc.
(2) DES modify its refuse processing facility to produce RDF ona
continuous basis and of quality acceptable to PEPCO.
(3) DES construct a pneumatic transport system capable of delivering
up to 20 tons per hour of RDF to PEPCO. The pneumatic piping
extending within PEPCO’s property should be donated or leased at
a nominal fee to PEPCO and maintained by PEPCO.
222
M { © SWRCNOA ©
NEW GATE AND ROAD SECTION
COOLING TOWER | |COOLING TOWER |||
TRUCK ROUTE
SWITCHYARD
: oe)
Pneumatic ~~_ BIN
conveyor
COAL
: STORAGE
eWesigyt E We) | Sy
so
(ie
LOO
———————
ley (alert to] fete
)
Fig. 2. Site plan of PEPCO Benning Generating Station indicating operational features
of option B. |
© swrc NOG
N TRUCK ROUTE i!
=:
— <4 —_— <= so a *‘
[a=]
f
1O).~e= OPPER a
Dee
ire : N
OBLR.NO.26 Fr Oy
O}pneumatic O/
conveyor 9 COAL
\ STORAGE
BLR. NO. 25 \
N
~=———--—
sotre TRUCK ROUTE
Se
Fig. 3. Site plan of PEPCO Benning Generating Station indicating operational features
of option C.
“5 O SWRC NO. 1 @
TRUCK ROUTE
eS SS SS
ge
| COOLING TOWER COOLING TOWER
i=] es]
vy Eves] ] (ees
y BLR. 28 | =
Fence to be ES
relocated BLR. NO. 27 cS a
HOPPER 8 Pneumatic Pag ae
BIN—= conveyor Srey, TELE ~—
& BLR. NO. 26 =
‘a COAL
; STORAGE
H |BLR. NO.25 \
SS
7 = je= Tape) &
OLD PLANT |
Die Cleric
Fig. 4. Site plan of PEPCO Benning Generating Station indicating operational features
of option D.
Ezz
a
SWRC NO.1
Pneumatic O ©)
conveyor
peed is
|| COOLING TOWER
sa
aed
a
=
cate
= BLR. NO. 26
CF COAL
4 ; STORAGE
A | BLR.NO.25 f IS
ple ee ince? Fy ©.
OLD PLANT |g
“
\
\
1
U
Jo Ooovoo
Fig. 5. Site plan of PEPCO Benning Generating Station indicating operational features
of phase II.
224
(4) An agreement between PEPCO and DES for a pilot project of five
operating years be executed.
(5) RDF be delivered at no charge to PEPCO during the first operating
year.
(6) Benefits to be shared equally during the remaining four years of
the initial agreement. 3
(7) The agreement be renegotiated at the end of the fifth operating year.
To avoid entagling this project in the larger and more complicated issue
of fuel pricing, it was reeommended that the net benefits be equalized. The
net benefit for each party would be based on benefits for four years less
capital costs and operating costs for five years. A benefit accrues to DES by
not having to incinerate or transport to landfill the weight of material sent
to PEPCO as fuel and PEPCO benefits by the savings in fuel costs from
substitution of coal with RDF.
The average net benefit is obtained by summing the DES and PEPCO net
benefits and dividing by two. The party with the highest net benefit then pays
the difference between its net benefit and the average benefit to the other
party.
The task force committee concludes that the project is an extremely
advantageous undertaking from both the DES and PEPCO standpoints and
offers a partial solution to the solid waste disposal problem within the District
of Columbia. ‘
During the planning process, the U.S. Environmental Protection Agency
expressed interest in the project as an opportunity to investigate the co-firing
of RDF with oil at low investment and within a relatively short time schedule.
Encouraged by EPA, in April, 1975, DES submitted a grant application for
partial federal funding of a greatly expanded project, with the remainder of
funding from DES and PEPCO.
The project submitted for partial federal funding is a different one. The
mutual benefit sharing aspects are not included; there is no payment for the
fuel during the grant period. The fuel acceptance provisions do not interfere
with the experimental nature of the project. First firing is planned approxi-
mately 16 months after grant award. Co-firing oil with secondary shredding
of RDF will be investigated first, before co-firing with coal without secondary
shredding. Plans include extensive monitoring of air emissions, including
analyses of heavy metals and various organic compounds. Project funding
and implementation are pending.
Resource Recovery and Conservation, 1 (1976) 225—233 225
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
UNION ELECTRIC COMPANY’S SOLID WASTE UTILIZATION SYSTEM”
DAVID KLUMB
Union Electric Company, St. Louis, Mo. 63166 (U.S.A.)
(Received 19th March 1975)
INTRODUCTION
Full scale testing to determine the feasibility of burning suitably prepared
solid waste in an existing pulverized coal fired utility boiler has been under-
way by the U.S. Environmental Protection Agency, the City of St. Louis,
and Union Electric Company since April 1972. Approximately 45,400
metric tons of St. Louis residential solid waste has been processed, providing
a burnable supplementary boiler fuel of approximately 36,000 metric tons.
On February 28, 1974 the Union Electric Company announced that it
would build, own, and operate a 7,300 metric tons per day solid waste utili-
zation system (SWUS) capable of utilizing essentially all of the solid waste
generated in the 1.2 X 10'°m? St. Louis metropolitan region with a popu-
lation of about 2.5 million. The SWUS is scheduled for full operation on
June 1, 1977.
The SWUS, estimated to cost $70 million, will be built with private funds.
Revenue to support the investment and to cover operating costs will be
generated by dumping fees, sale of recovered metals, and sale of the burnable
fraction of the solid waste. The Union Colliery Company, a wholly owned
subsidiary of Union Electric, will build, own, and operate the system and no
monies to finance the system will come from the parent Company’s elec-
tricity customers.
GENERAL DESCRIPTION
The St. Louis region covers 1.2 X 10'° m? and includes two states and
seven counties in addition to the City of St. Louis. The region includes more
than 150 governmental units and 150 public and private waste haulers. Cur-
rent solid waste practices include landfill, incineration, and roadside and
promiscuous dumps. Current solid waste generation including residential,
commercial, and industrial waste is estimated to be approximately 7,300
metric tons (mt) per day. The projection for 1980 is 9,000 mt per day.
*Paper presented at the Symposium ‘“‘Energy Recovery from Solid Waste’’, March 13—14,
197 5.
226
Union Electric Company is an investor-owned electric utility franchised
to generate and distribute electricity in the eastern portion of Missouri and
small areas in Illinois and Iowa. More than 90 percent of the Company’s
electricity is generated at pulverized coal-fueled steam-electric generating
plants. The two power plants of particular interest to SWUS are the 2,400
MW Labadie Plant 60 km west of St. Louis and the 900 MW Meramec Plant
about 32 km south of St. Louis. Coal consumption at Labadie is about 900
mt per hour and at Meramec about 360 mt per hour.
The St. Louis region is provided with railroads which radiate from the
center of St. Louis like spokes in a wheel. Interstate highways and four-lane
arterial roads also radiate from the core city and also encircle the metro-
politan area. This railroad and road network, along with the remote location
of the coal-fired power plants, provides for the efficient truck collection and
rail transport of solid wastes to the isolated power plants.
Figure 1 is a diagramatic representation of the Solid Waste Utilization
System. The previous arrangement for burning the refuse-derived fuel with
coal (now operating under an EPA demonstration grant to the City of St.
Louis) has been described [1].
Collection Truck
Collection
and transfer ?
station
Boiler/Furnace
| | pel Storage Bin
Packer ‘Container
2 Containers per Flat Car Air Classifier
Rail transit
Power plant li
Fig.1. Flow chart of Union Electric Company’s planned solid waste utilization system.
Union Colliery Co., a wholly owned subsidiary, will build, own, and operate the S.W.U.S.
Glass & Non-
Magnetic Materials 4
Coal
€ Precipilator
Ash to Storage Pond
COLLECTION AND TRANSPORT
A totally owned subsidiary, the Union Colliery Company, will operate
the SWUS but will not collect the solid waste where it is generated. Public
and private trash haulers will be offered disposal service at five truck-to-rail
transfer stations. These transfer stations will be located on arterial highways
and/or interstate highways to preclude heavy truck traffic in or near residen-
tial areas.
A typical truck-to-rail transfer station will have a capacity of from about
1,300 to 1,800 mt per day. The smaller station can be expanded to the lar-
ger capacity. Residential, commercial, selected industrial, and selected demo-
lition solid wastes will be accepted at transfer stations. Tires, appliances,
demolition lumber, yard wastes, and size-reduced trees and trimmings will
be accepted. Those wastes determined to be physically detrimental to the
SWUS or classified to be hazardous to be handled in the SWUS by govern-
mental agencies will be excluded. Only licensed trash haulers will be allowed
to dump.
Trucks will be weighed before entering the totally enclosed transfer station
building. A plan of a typical transfer station in shown in Fig.2. The trucks
will enter the building and be directed to dump in conveyor dumping pits or
on the floor, depending upon truck flow. All sizes of commercially available
trash trucks will be able to use the facility including large (75 yard? = 57m?)
transfer trailer trucks.
Front-end loaders will lead the solid waste from the tipping floor to the
stationary compactor conveyor. The front end loaders will also be able to
tow a stalled trash truck if it breaks down in the building or on building
BH ep
mae &
"aN 9 Zui, - ees — - =
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eee ss EE REE: Pag (4 > gh
Pre a Or 7 ‘ne y 3 (ag
2 ZB
Ze
2 ae
"7, FOXY, bd Ts ie
=
Fig.2. Typical transfer station plan. Site area approx. 90 X 10° m’.
228
access roads. Present plans are to accept waste 16 hours per day, six days
per week. Hours of operation will be scheduled to meet the demands of the
haulers.
The solid waste will be loaded into 76 m? (100 yard? ) containers by con-
ventional stationary packers having a nominal capacity of about 8m°. No
solid waste storage will be provided for in the stationary compactor con-
veying pit and there will be only peak dumping storage on the tipping floor.
Sufficient packer capacity is being provided to handle normal delivery, with
only 2 to 3h of peak delivery capacity being provided on the tipping floor.
The solid waste shipping containers are designed for a nominal capacity
of about 69m°. The design is similar to conventional end-loading solid waste
transfer trailer bodies. Two containers will be loaded on a conventional con-
tainer on flat car. With a tare weight of about 9,000 kg (20,000 lb.) the con-
tainer will carry a net solid waste payload of from 32 to 36 mt (35 to 40
tons).
The containers will be built to ISO and AAR standards for ship-board
containers and can be carried on conventional ship container truck trailers.
The 12m (40 ft.) long containers will be equipped with a telescoping cylinder-
operated ejection blade and a guillotine loading door.
The container will be set on a movable steel framework which will lock
the container to the stationary packer. The loading door will be operated
by hydraulic cylinders. Load cells in the container positioning frame will cut-
off the packer when the container is full.
The containers will be handled by conventional container handling vehicles.
For short-term storage the containers can be stacked two high when full and
three high when empty. Normal operation will provide for loading 36 to 50
containers on 18 to 25 rail cars per transfer station per day.
Two solid waste unit trains per day will deliver up to 5,500 mt per day to
the Labadie processing plant via two different railroads. Approximately
900 mt per day will be delivered to the Meramec process plant on a single
unit train by one railroad.
PROCESSING FACILITIES
The SWUS is being designed to provide a nominal processing capacity of
6,000 tons (approximately 5,500 mt) per day at the West (Labadie) facility
and 2,000 tons (approximately 1,800 mt) per day at the South (Meramec)
facility. Maximum peak processing capability will be 9,600 tons per day
(8,700 mt) at the west facility and 3,600 tons per day (3,300 mt) at the
south facility. Both processing facilities will be able to accept truck-delivered
solid waste. |
Containers at the processing plants will be handled by container handling
vehicles. Placed on container unloading frames, the containers will be un-
loaded by ground mounted telescoping cylinders which will operate the con-
tainer ejection blade.
229
The west processing facility will include four processing lines, each having
a capacity of 100 tons (90 mt) per hour. The south facility will include
three lines. Each facility will have a redundant processing line to provide
for hammermill maintenance. Figure 3 is the preliminary process flow dia-
gram for the west facility.
PRIMARY SECONDARY
SHREDDERS MAGNETIC GLASS SHREDDERS AIR STORAGE
6” SIZE GRIND SEPARATORS SEPARATORS 3/4” GRIND SIZE CLASSIFIER
5 TPH
2 rie TO UNIT 1and/OR 2
PROCESSING el 100 TPH (MAX)
LINE -1 .
25 TPH/ BURNER
TO UNIT/2and OR1
TOO TPH (MAX)
25 TPH BURNER
5TPH
as
> > can
PROCESSING
LINE-2
1 160 TONS
*{3WAY) (80 FT. DIA.)
ee
6.000 TPD . Ky
1.800.000 TPY C7
172 CONTAINERS
86 RAIL CARS
PROCESSING
LINE-3
100 TPH (MAX)
it
25 TPH/BURNER
ONE SPARE PROCESSING LINE
PROCESSING
LINE-4
TO UNIT 4 and OR 3
100 TPH (MAX)
25 TPH/ BURNER
|
160 TONS
*(oway) | (@OFT.DIA.)
N
x
<==
THREE LINES IN SERVICE
24 HOURS PER DAY BURN
6 DAYS PER WEEK
3 UNIT TRAINS PER DAY
NORMAL PLANT BURN -200 TPH
ORGANIC
HEAVES
PROCESSING
TO STORAGE
115 TPH
, BINS
PROCESSING
PRIMARY AND SECONDARY
SHREDDERS FOR LABADIE AND
MERAMEC OF SAME SIZE, BUT
DIFFERENT MOTOR SIZE
2.5 TPH
FUEL
4800 TPD, 1.440.000
MAG NETICS
500 TPD, 150000 TPY
p--&-----e--4
'TO FILL 30 TPH
i mee ie in
ROCK, ETC.
TO
=
500 TPD
O O
MAGNETICS BULK SOLID WASTE
RAIL CARS 6.000 TPD, 1.800.000 TPY
(= 750.000 TPY COAL)
2.5 TPH
MAGNETIC
SEPARATORS)
GLASS
NON-FERROUS
METALS
GLASS
600 TPD. 180.000 TPY
BOTTOM ASH, 150 TPD
(-45 TPD COAL ASH)
ROCK. ETC
SO TPD,15.000 TPY
FLY ASH, 600 TPD
(- 210 TPD COAL ASH)
Fig.3. Preliminary flow diagram for west process facility.
The first stage, reversible, auto shredder type, horizontal shaft hammer-
mill will reduce the solid waste to a nominal 6-in. size. The first stage will be
2,000 hp (1.5 MW).
The first stage mill product will be conveyed to magnets for separation of
magnetic metals. Both belt and drum magnets are being investigated.
The magnetic metals will be sold to a secondary metal processor for de-
tinning and production of tin and No.1 bundle steel scrap.
The coarse milled waste, including less magnetic metals, will be conveyed
to a glass removal device. This device has not yet been selected. Investiga-
tions have been underway for the past few months to develop a conveyor
and sizing device. Such a device appears to be commercially available; it is
230
expected to remove about 50 percent of the glass and grit.
The 1250 hp (0.9 MW) second stage, horizontal shaft hammermills will
produce a 3/4 to 1 in. (1.9 to 2.5cm) product size. The mill discharge will
be conveyed to air density separators for classification into burnable and
unburnable fractions.
At the west facility, there will be two air classifiers for each of the four
second stage mills, each with a capacity of 50 tons (45mt) per hour. The
south facility second stage mills will each feed a single 50 tons per day air
classifier.
The burnable fraction from the air classifier will be air transported to live
bottom surge bins. At the west facility there will be 4 bins each with an out-
feed capacity of 100 tons (91 mt) per hour via four outfeed chutes, as shown
in Fig.3.
The west facility surge bins will be equipped with 4 outfeed systems. Each
outfeed system will include two drag chain conveyors set into the circular
floor on 45° centers. The two conveyors feed into a common chute which
feeds the solid waste into a pneumatic, boiler charging system.
The surge bins provide only limited storage. At a boiler firing rate of from
80 to 100 tons (73 to 90 mt) per hour there will be only from 1/2 to 1 hour
storage in each bin.
At the south facility, the existing experimental prototype bin that has
been in service three years will.be modified to provide for higher capacity
and will be direct current powered. A new four conveyor bin will be used to
provide firing tc the two boilers at Meramec that were not used in the proto-
type. The south facility bins will be equipped with 4 outfeed conveyors and
the new bin will have a capacity of about 60 tons (54 mt) per hour.
BOILER CHARGING SYSTEMS
The boilers at the south facility Meramec Power Plant include: two
140 MW, combustion engineering (CE), tangentially fired units; a 250 MW,
Foster Wheeler , front-fired boiler; a 300 MW Foster Wheeler front fired
boiler. All are fired with pulverized coal and are equipped with electrostatic
precipitators.
The Meramec unit 1 and 2, CE boilers are presently equipped with 4 solid
waste (SW) burners per boiler. These will be relocated to deliver the refuse-
derived fuel just above the top level of coal burners. One SW burner will be
located in each corner of the boiler furnace at the top of the coal burner
assembly.
The SW burners for Meramec units 3 and 4 will be installed in the front
wall of the furnace above the top row of coal burners. There will be four
burners in unit 3 and four burners in unit 4.
The boilers at the west facility Labadie Plant include 4,600 MW, CE,
tangentially fired, pulverized coal boilers. All are essentially identical. Each
boiler will be equipped with 4 SW burners, one per corner. The burners will
be installed just above the top coal burner in the coal burner assembly.
The boiler charging system for each burner consists of one rotary air
feeder, positive displacement blower, and piping from the feeder to the boiler
burner. The infeed chute to the rotary air lock feeder is fed from one or
more surge bin conveyors.
Because the SW will contain residual ground glass and some metals the
SW piping will be installed with removable wear-back elbows. Ceramic lined
fiberglass pipe is currently being investigated for the straight sections of the
transport piping. The ceramic lined pipe is considerably lighter than plain
carbon steel pipe and appears to have good anti-abrasion characteristics.
The boiler charging system is being designed to provide up to 20 percent
of the full load heat input requirement of each boiler. The 8,000 tons per
day (7,300 mt) SWUS processing capacity can provide full firing at 10 per-
cent of full load heat input. Thus, there is redundant boiler capacity.
SOLID WASTE CHARACTERISTICS
Table 1 gives the analyses for 380 samples of air-classified solid waste.
Note that the figure for NaCl should be subtracted from the figure for total
chlorides to give an analysis for organic chlorides. It is apparent that the re-
fuse-derived fuel does not contain critical levels of organic chlorine (mea-
sured this way) which will be released during combustion (NaCl decomposes
at 1650° C; furnace temperatures are of the order of 1370° to 1480°C). More
than 75 percent of the chlorine in refuse-derived fuel can be accounted for
as NaCl. The analytical methods have been described [2].
The density of the refuse-derived fuel after milling to 1.9 cm varies from
64 to 112 kg/m? (4 to 7 lb./ft.3), loose. However, when placed in storage
to depths of from 9 to 12 m (380 to 40 ft.), the density increases to as high
as 400 kg/m? (25 lb./ft.? ). Moisture content and particle size have a signifi-
cant effect on density and flow characteristics and these characteristics vary
from day to day and through the system.
ENVIRONMENTAL IMPACT
Careful evaluation of the environmental impact of the SWUS has been
underway since initial operation of the prototype. Boiler gas emission tests
conducted independently by the U.S. Environmental Protection Agency and
Union Electric during November and December of 1973 disclosed no serious
emission problems.
Certainly when compared to disposal by landfill or incineration the SWUS
appears to offer significant advantages. Conservation by recycling metal re-
sources such as tin, steel, copper, and aluminum offers a significant environ-
mental advantage over disposal.
232
TABLE 1
Air-classified refuse analyses”
380 samples taken November 9, 1973 through December 10, 1974
As fired basis
Moisture Ash Sulfur Total Nacl? J/kg
(wt %) (wt %) (wt%) chlorides (wt%) x10°°
(wt %)
Average Dae) 18.5 0.11 0.34 Or 11.6
Maximum 63.0 53.8 0.31 0.94 0759 ow
Minimum 3.0 7.6 0.02 0.13 0.10 513
Air-classified refuse ash (wt %)
Average Maximum Minimum
PO: 1B 2.04 0.41
siO, 52.8 66.6 39.9
Al,O, a 26.90 3.43
TiO, 0.89 eS) 0.07
Fe,0, 6.40 Dee US Dsi5yi}
CaO 12.06 16.50 6.92
MgO 1.48 3.17 0.22
so, IS) 3.75 0.54
K,O 1.68 2.91 0.89
Na,O S22 19.20 Seti
SnO, 0.034 0.10 0.001
CuO 0.21 1.74 0.03
ZnO 0.34 DPS 0.09
PbO O19 0.73 0.04
a
piinalyses by “Research 900” Division of Ralston Purina Company, St. Louis, Mo.
NaCl percentage is subtractable from total chlorides.
ECONOMICS
The SWUS is being built as a free enterprise, profit making venture. The
risk capital to build the system will come from private investors. The SWUS
must attract the public and private haulers by offering a dumping service at
lower overall cost than any competing service.
The economics of scale, low unit train point-to-point rail transport costs,
sale of metals, and the sale of the burnable fraction of the solid waste will
provide the revenue to support the investment.
CONCLUSION |
The SWUS is expected to provide an environmentally sound economic
—_
or
system to utilize the materials available in the solid waste stream. It will
significantly reduce the water, air, and esthetic degradation of the environment
which is too often a product of poorly managed landfills. SWUS will provide
for conservation of irreplaceable fossil fuels and metals, and it will provide
these benefits within the framework of the free enterprise system.
REFERENCES
1 Dille, E.K., Klumb, D.L. and Sutterfield, G.W., 1973. Recycling Solid Waste for Utility
Fuel and Recovery of Other Resources, .In: Frontiers of Power Technology, Oklahoma
State University, October 10—11.
2 Lowe, R.A., 1973. Energy Recovery From Waste, U.S. Environmental Protection
Agency, Washington, D.C.
3 Klumb, D.L., 1974. Solid Waste Prototype for Recovery of Utility Fuel and Other Re-
sources, Air Pollution Control Association, Denver, Colo.
4 Klumb, D.L. and Brendel, P.R., 1974. Union Electric’s Solid Waste Utilization System,
American Society of Chemical Engineers, Salt Lake City, Utah.
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Resource Recovery and Conservation, 1 (1976) 235—243
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
DESIGN AND POLLUTION CONTROL FEATURES OF THE SAUGUS,
MASSACHUSETTS STEAM GENERATING REFUSE--ENERGY PLANT *
WALTER K. MACADAM
Wheelabrator-Frye Inc., New York, New York 10017 (U.S.A.)
(Received 24th March 1975)
INTRODUCTION
A steam generating plant using refuse for fuel is being constructed at
Saugus, Massachusetts which, on completion, will dispose of an average of
1,089 metric tons (1,200 tons) of refuse a day from some 16 communities
north of Boston and provide energy to a nearby industrial plant for electric
power generation and process steam. The system is an application of the
Von Roll type water tube cooled boiler system with stepped grates, firing
refuse essentially as received without the use of auxiliary fuel. Several recent-
ly developed features are incorporated in the design to improve reliability
and availability under the relatively high steam temperatures involved. The
plant is constructed to meet stringent pollution control standards for odor,
particulates, gas, noise and water emission, and will provide essentially com-
plete refuse combustion without the need for auxiliary fuels. Clean metals
and sterile ash suitable for road fill will be recovered initially and provision
is being made for expansion of materials recovery sub-systems in the future
as markets and technology make them economically viable. The design also
contemplates future doubling of all plant capacity to 2,177 metric tons
(2,400 tons) per day.
An unusual feature of the plant is that it is privately financed, owned and
operated and will pay real estate and income taxes. Severe requirements for
continuity and reliability of refuse acceptance have been imposed, since the
landfill currently available to the communities will be permanently closed
for environmental reasons as soon as the plant goes into operation. In addi-
tion, the demand for continuity of steam generating capability emphasizes
reliability in the system design and calls for the provisions of adequate stand-
by facilities. |
Ground was broken for the Saugus refuse energy plant in June 1973, with
initial operation scheduled for mid-1975. The 16 communities, with a com-
*Paper presented at the Symposium “Energy Recovery from Solid Waste’”’, March 13—14,
1975.
bined population of approximately 500,000, are expected to make their
own arrangements for refuse delivery to the plant weighing station and will
pay a tonnage fee for disposal. Complete and sanitary combustion of the
refuse will produce more than 900,000 metric ton of steam a year for sale to
the General Electric Company (GE) manufacturing plant at Lynn, Massa-
chusetts, across the Saugus River. This energy sale will help reduce disposal
charges to the communities and at the same time reduce fuel oil requirements
by approximately 260,000 liters (70,000 gallons) a day. It is significant that
a net improvement in air pollution conditions will result, since the sulfur and
particulate emission from the refuse plant will be even lower than for the
facilities being replaced which burn low sulfur fuel oil.
BACKGROUND
The need to provide a modern and clean refuse disposal system became
apparent in the Boston North Shore area when state environmental and
other requirements resulted in a court order to close down a large sanitary
landfill operation in the tidelands at Saugus, Massachusetts serving the area
communities.
The project is privately financed, owned and to be operated by the Refuse
Energy Systems Company (RESCO), a joint venture of Wheelabrator-Frye
Inc. and M. DeMatteo Construction. The system design and construction
management is being carried out by Rust Engineering Company of Birming-
ham, Alabama, a subsidiary of Wheelabrator-Frye, and construction is being
undertaken by DeMatteo Construction. The plant design concept is based on
Wheelabrator’s exclusive license with Von Roll, Limited of Switzerland and
is an updated version of, and similar in operation to other Von Roll refuse-
energy plants in Europe, Australia, Japan and Canada. In the Saugus situation,
however, it meets generally more severe environmental requirements, makes
use of several new features involving advanced technology, and meets a num-
ber of specialized demands imposed by site conditions and unusual require-
ments for reliability and continuity of refuse acceptance and steam produc-
tioned.
Low operating cost over the life of the plant is considered essential as a
protection against inflation. The estimated total initial capital cost of approx-
imately $30 million for the plant recognizes these requirements and special
conditions and includes land, maintenance shops, roads, weighing stations,
vehicles, spare parts, utilities bridge and a 0.8 kilometer pipe line system ex-
tending across the Saugus River for steam delivery, condensate return and
electric power.
SPECIAL REQUIREMENTS
As noted previously, there are a number of unusual conditions and require-
ments placed on the design of the plant and reflected in the cost. These can
be summarized as follows:
— The present landfill site has been ordered closed and cannot continue in
operation after plant completion. For this reason an unusually large storage
pit (6,100 metric tons capacity) is provided to accumulate refuse during shut-
down of a boiler for maintenance or repairs.
— Since the plant is constructed on the landfill, the site conditions are poor,
requiring all major structures to be supported by piles driven to bedrock,
some 24 meters below.
— The communities prefer a single type of collection as a cost saving
measure. As a result, minimum selectivity will be exercised at the plant in
accepting refuse and garbage, provided it has domestic or commercial origin.
Stoves, tires, mufflers, furniture, auto wheels, pipes, etc. will be taken as
normally present in municipal refuse.
— The steam delivery contract to GE requires not only standby oil jets in
the main boilers, but also two auxiliary standby oil fired boilers.
— No intake or discharge is permitted to the river.
— A utility bridge and pipe line system is required to transmit steam across
the Saugus River.
— Local air pollution control requirements are more stringent than Federal
standards.
BASIC REQUIREMENTS
The basic requirements are to accept an average of 1,089 metric tons per
day of domestic and commercial refuse and provide steam to the General
Electric Company at 4,309 kPa (625 psig) and 418—441°C (785—825°F).
These steam conditions were selected to coordinate with the output of
existing boilers in the GE plant [2]. Operation is 24 hours a day, 7 days a
week. Peak steam delivery is 159 metric tons per hour and not les than 29.5
metric tons per hour. A minimum of 90,000 metric tons of steam will be
delivered annually.
A dump charge will be made with escalation corresponding to half the
change in the local labor wage index. Steam charges are based on providing
somewhat lower energy cost to GE than would be involved if oil were used
as a fuel. Steam charges will escalate with oil price increases.
SYSTEM DESCRIPTION
The physical layout of the plant and its geographical proximity to the
steam customer is illustrated in Fig. 1. Refuse trucks will pass a weighing
station and move up a paved earthfill ramp to a receiving area. Here the
trucks are backed to the plant entrance doors and refuse is deposited in the
6,100 metric ton-capacity pit.
A simplified cross section of the plant is shown in Fig. 2. In general con-
figuration this is similar to other refuse boiler plants except for the stepped
grates and the pendant, vertically oriented tubes in the convection section.
238
UTILITIES BRIDGE
ee 1. TRANSFERS STEAM TO GE
2. TRANSFERS FUEL OIL, BOILER
af FEEDWATER, AND ELECTRICAL
ra, POWER TO RESCO
ee AC
RIVER
Fig. 1. Physical layout of RESCO.
ee F ct F
-s
=: Se On SSS
Fig. 2. Wheelabrator-Von Roll refuse—energy system.
The pit is served by a traveling crane system which serves the furnace feed
hoppers and also permits mixing refuse as required to promote uniformity.
Some unusually bulky refuse, such as furniture, will be transported by crane
to a 895 kilowatt (1,200 horsepower) fragmentizing hammermill which will
239
reduce the largest dimension to about 0.3 meters and discharge tne frag-
ments back into the pit.
Two steam generators are provided initially, with a maximum capacity of
680 metric tons per day each, for refuse with a heat value of 10.5 MJ/kg
(4,500 BTU/Ib.), Lower Heating Value. Provision is made for the addition of
two similar boilers at a later date. Two oil fired package boilers are also
provided as standby units with a total capacity of 108.9 metric tons per hour.
In each furnace, refuse is burned on a Wheelabrator/Von Roll reciprocating
grate system without the use of an auxiliary fuel. This consists of three grates
separated by steps over which refuse tumbles to provide complete combustion.
Combustion gas temperatures are in the range of 540—980°C. Under-fire and
over-fire air volume and temperature as well as individual grate operating
speeds are controlled to suit conditions and assure complete burnout. Much
of this control is automatic.
The flue gas and furnace radiation heats the water walls of the boiler.
Heated flue gases then pass through the convection section and come in con-
tact with pendant boiler tubes. Dust and scale buildup is controlled by a
specially designed boiler tube rapping mechanism. The system involves
periodic striking of the lower side of vertical boiler tube sections with a
hammer mechanism. Such operation dislodges dust buildup on the tubes
without disturbing the protective oxide coating on the tube exterior. This
recent development eliminates corrosion problems from soot blowers and
makes it unnecessary to shut down the boilers for periodic tube cleaning.
The cooled gases pass to two Wheelabrator-Lurgi electrostatic precipitators
[3], operating at approximately 99 percent efficiency, designed to reduce
the particulate emission to 5.7 X 107* kg/m? (0.025 grams/standard cubic
foot) corrected to 12 percent CO, (0.05 required). These are described in
more detail later in the section covering pollution control. Cleaned exit flue
gas is discharged to the atmosphere through a concrete stack 54.3 meters
(178 feet) above grade.
Fly ash collected by the precipitators, riddlings and clinkers are water
quenched and passed by conveyor to a rotating screen. Bulky metals are
separated for sale and the bottom ash screenings are further subjected to mag-
netic separation. This permits sale of the remaining ferrous metals. The resid-
ual ash (about 160 metric tons per day) will be sold or used as road fill or
deposited in a specially designated disposal area nearby. Quench water is dis-
charged in wet ash or evaporated. Blowdown water is almost entirely con-
sumed by transfer to the quench tanks.
FINANCING
Initial financing was arranged through Wheelabrator Financial Corporation,
a subsidiary of Wheelabrator-Frye. This financing of the plant construction
is not contingent on any signing of refuse disposal contracts with the munic-
ipalities. Subsequent debt financing is being arranged through tax exempt
industrial revenue bonds.
240
ESTABLISHMENT OF DUMP CHARGES
Dump charges, or so-called tipping fees, are based on individual agreements
with municipalities. It is contemplated that initial charges will be lower for
longer term contracts and that escalation of rates will be based on one half
the rate of change in the local labor rate index. RESCO has joined a number
of the communities in obtaining the services of the Mitre Corporation, a not-
for-profit corporation headquartered at Bedford, Massachusetts, to examine
the costs of the project and to determine the appropriateness of the proposed
charges, considering costs and risks. This has resulted in a contract structure
and pricing schedule adjudged fair to all concerned.
TECHNOLOGY
The RESCO project is designed to make use of updated technology applied
to established concepts proven by full scale experience in similar situations.
The importance of reliability, continuity in refuse disposal, pollution control
and steam generation were the principal factors in utilizing the total com-
bustion system concept supported by substantial experience in Europe,
Canada and Japan. No wholesale shredding of refuse is required, thus saving
shredding costs estimated in excess of $3.00 per ton and eliminating fire and
explosion problems [4—6].
The 5.3-hectare (13-acre) site and plant layout has been arranged for
maximum flexibility and to permit future construction of additional resource
recovery subsystems, either at the front end or back end of the energy recov-
ery unit when and if the technology, economics, experience and market
shows this to be a viable and reliable operation.
POLLUTION CONTROL DESIGN
Odor control
Odor control was an important consideration in both the construction and
operation of the Saugus plant. Since the facility is being built on a sanitary
landfill site covered by a layer of deposited refuse approximately 3.7 meters
(12 feet) thick, unusual measures had to be adopted during excavation for
the plant foundations and truck receiving area. A total of approximately
46,000 cubic meters of refuse material had to be removed to another area in
the existing landfill and covered daily with a layer of earth. Deodorizing
units, consisting of 19 liter (5 gallon) pails equipped with wicks and filled
with Air Kem water soluble deodorizing fluid, were placed at intervals of
about 15 meters to the windward side of the removal operation. Earth fill
was placed in the excavation in a concurrent operation to minimize exposure.
These procedures were carried out under permission and inspection of the
Massachusetts Bureau of Air Quality Control.
Refuse odors during plant operations will be closely controlled by dumping
all refuse into the indoor storage pit. A system of negative pressure will draw
fresh air through the entrance into the pit enclosure from which it is drawn
into the furnaces for use as combustion air. Furnace gas temperatures are
maintained in the range of approximately 540—980°C, destroying odors in
the combustion air and those emitted by burning refuse. The main control
room, administrative space and crane operator consoles are enclosed and air
conditioned to produce a temperature and odor controlled environment.
Control of particulates
Fly ash and particulates in the flue gas will be reduced well below levels
specified by federal, state and local requirements. This is accomplished by
means of collection hoppers under the boiler convection sections, followed by
Wheelabrator-Lurgi electrostatic precipitators. Precipitators were chosen in
place of wet scrubbers for reliability and to minimize generation of a steam
plume from the stack caused by introduction of additional moisture. An
individual, dry bottom precipitator is provided for each steam generating
unit. Each will handle 6,800 cubic meters per minute of flue gas at 220°C to
surpass the stringent Metropolitan Boston Air Pollution Control District
requirements of 11.4 X 10°* kg/m? (0.05 gr/scf), corrected to 12 percent CO,.
The precipitators are designed to control particulates to 5.7 X 10™* kg/m?
(0.025 gr/scf) and, therefore, are sized to operate at an efficiency of approx-
imately 99 percent.
The reliability and continuous availability of the precipitator units are en-
hanced by employing discharge electrode rods welded into rectangular pipe
frames in such a manner that the electrodes are firmly attached at points
separated by no more than 1.5 meters. The rigid support system was con-
sidered to offer advantages over a system using weighted hanging wires by
providing improved strength and controlling electrode failure due to mate-
rial fatigue, corrosion or oscillation. Any additional cost was considered to
be outweighed by advantages from the standpoint of maintenance and con-
tinuity of operation.
Air quality
Since refuse is a low sulfur fuel, typically with only about 0.1 percent
sulfur content, no special measures will be required to remove this component.
To fully disperse the exit gases, which consist almost entirely of nitrogen,
carbon dioxide and water vapor, a 54 meter (178 foot) concrete stack is being
employed, 2.7 meters (9 feet) in diameter at the top. No problems with
chloride emission are foreseen, based on experience with similar installations
[7]. Flame temperatures are kept below the level at which nitrogen oxides
would be produced in any significant quantity. Based on experience with
similar installations, these emissions are expected to be much lower than the
242
0.13 kg/10? J (0.3 pound/10° BTU) input permissible for liquid fossil fuel
fired systems. Because the standby oil fired boilers are planned to be operated
on low sulfur oil when no refuse is available, and will meet emission require-
ments, permission has been obtained to exhaust through smaller stacks ex-
tending over the roof, approximately 38 meters above ground level. Smoke
density requirement of less than Ringelmann No. 1 will be met.
Ambient particulate levels have been calculated using Weather Bureau data
and predicted emissions from the stack, using a computer program developed
by Rust Engineering on the basis of ASME procedures. Predictions for one-
hour concentrations under least favorable conditions indicated that the addi-
tion of the stack emissions to existing annual averages would not exceed the
allowable value of 75 micrograms per cubic meter. Actually, operation of the
refuse-energy plant should produce no net impairment to the average ambient
level since this includes the GE plant present emissions, which will be reduced
when the refuse plant becomes operational.
Water quality
Water for steam production, cooling, and ash quenching will be obtained
from the municipal supply in addition to that needed for the sanitary system.
Some steam condensate is to be returned over the utility bridge and optimum
recirculation and treatment is provided to minimize input water requirements
and effluent discharge. No river water will be circulated or used.
Waste water sources are the sanitary system, boiler blowdown, demineralizer
backwash, and quench channel overflow. All blowdown and backwash,
neutralized as required, is pumped to a holding tank which feeds the ash
quench conveyor channels. No ash quench water is recirculated since it is
progressively removed in the wet ash with overflow to the sewer. Under
operating conditions, total flow to the sewer is expected to consist primarily
of the sanitary system discharge.
Noise control
Most of the machinery that would make any appreciable contribution to
the noise level in the area of the plant is housed within the plant buildings.
The exceptions are the refuse boiler I.D. fans which are located between the
precipitators and the stack and the trommel screens located in the ash handling
system.
An ambient noise level survey was performed prior to the start of construc-
tion, and calculations have been prepared to show anticipated noise levels
when the plant is in operation. Application for permits have been filed, and
it is anticipated that the plant will meet all necessary requirements.
CONCLUSION
Unusual construction conditions and the need to provide essentially un-
243
interrupted availability of refuse reception, control of pollution and steam
generating capacity has resulted in specialized adaptations in the design and
pollution control measures for the Saugus Refuse Energy System. It should
provide an example of a multi-community refuse disposal service operated in
an environmentally sound manner on a private enterprise basis and privately
financed. Significant and important elements of the system plan included the
cooperation of a large industrial energy user and the decision to employ a
design based on demonstrated concepts with minimum preprocessing and
selectivity of refuse input.
REFERENCES
1 MacAdam, W.K. and Standrod, Jr.,S.E., 1975. Design and operational considerations
of a plant extracting energy from solid waste for industrial use. Presented at ASME
Industrial Power Conference, Pittsburgh, Pennsylvania, May 19—20. Copies available
from ASME Order Department, United Engineering Center, 345 E. 47th St., New York,
N.Y. 10017 (paper no. 75-IPWR-3).
2 Howard, A.H., 1975. The use of solid waste as a fuel to generate steam for an industrial
plant. Presented at ASME Industrial Power Conference, Pittsburgh, Pennsylvania, May
19—20. Copies available from ASME Order Department, United Engineering Center,
345 KE. 47th St., New York, N.Y. 10017 (paper no. 75-IPWR-11).
3 Engelbrecht, H.L. and Graves, N.D., 1975. Electrostatic precipitator installation for a
low-odor recovery boiler. Presented at the 68th APCA Annual Meeting, Boston,
Massachusetts, June 15—20. Copies available from APCA Order Department, 4400 Fifth
Avenue, Pittsburgh, Pennsylvania 15213 (paper no. 75-662).
4 U.S. Environmental Protection Agency, 1974. Second report to Congress — Resource
Recovery and Source Reduction. U.S. Government Printing Office, Washington, D.C.
5 Hughes, O.G., 1974. The Cringle Dock pulverisation and transfer station, London.
The 1974 Australian Waste Management and Control Conference: The Conference
Papers, Department of Fuel Technology, University of New South Wales, Sydney,
Australia.
6 Fales, E., 1974. Now giant grinders gobble our waste problems. Popular Science,
February.
7 Vaughan, D.A., Miller, P.D. and Boyd, W.K., 1974. Fireside corrosion in municipal
incinerators versus PVC content of the refuse. Proceedings of 1974 National Incinerator
Conference: Resource Recovery Thru Incineration, The American Society of Mechanical
Engineers, New York, N.Y. 10017.
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Resource Recovery and Conservation, 1 (1976) 245—255 245
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
AN EVALUATION OF METHANE PRODUCTION FROM SOLID WASTE*
R.G. KISPERT, S.E. SADEK and D.L. WISE
Dynatech R/D Company, A Division of Dynatech Corporation, Cambridge, Mass. 02139
(U.S.A.)
(Received 19th March 1975)
ABSTRACT
A technical and economic evaluation of a process to convert municipal solid waste to a
pipeline quality gas has been carried out, based upon a previously reported conceptual de-
sign for a 907 metric ton/day (1000 tpd) facility. The process design is shown to be tech-
nically within the state of the art, although economically acceptable operating parameters
are at the upper limit of today’s technology. The calculated baseline gas cost of $0.074/m?
($2.09/mcf) is economically acceptable when compared with projected costs of synthetic
gas or alternative fuels. Experimental priorities to demonstrate the commercial feasibility
of the process are established.
INTRODUCTION
Because of the two problems of need for supplemental sources of fuel gas
and concern about municipal waste disposal, considerable interest has recent-
ly been shown in the related solution of applying anaerobic digestion to muni-
cipal solid wastes. The digestion of the organic matter in municipal refuse can
be carried out much as the digestion of sewage sludge is done. The organic
matter in typical solid waste is observed to be predominantly cellulose; there-
fore, the chemical conversion and stoichiometry of concern may be repre-
sented by
C;H,,»O; +H,O > 3 CO, +3 CH, (1)
In the process for preparing methane from municipal waste, the organic mate-
rial is slurried with water and inoculated with the proper microorganisms. This
inoculation is spontaneous in an operating digester since organisms are already
present. The organic matter is partially solubilized or digested and then fer-
mented, forming methane gas, carbon dioxide and a residue of undigested
material. Under these circumstances 1 kg of chemically convertible waste will
yield 0.41 m® (1 lb > 6.65 ft.*) of methane at standard conditions of tem-
perature and pressure [1]. The methane will be accompanied by an equal
volume of carbon dioxide. The methane is scrubbed free of carbon dioxide
*Paper presented at the Symposium “Energy Recovery from Solid Waste’’, March 13—14,
OTD:
246
and traces of hydrogen sulfide, then dried. The undigested residue is disposed
of by incineration or landfill. Ferrous and non-ferrous metals and glass may
be recovered prior to digestion, if that is economical.
Previous studies have focused attention on the scientific and the economic
feasibility of the process, and the conceptual design of a 907 metric ton/day
(1000 tpd) facility [2—8]. It is presently projected that pipeline-quality gas
can be produced commercially with a selling price of $0.074/m? ($2.09/mcf),
based on an American Gas Association public utility financing scheme
(Table 1) [9,10]. An evaluation of the energy balance indicates that oper-
ating energy requirements consume the equivalent of only 37.5 percent of the
gas produced [2].
TABLE 1
Summary of base-line gas cost items
$/m* $/mef
Contribution of capital costs to gas cost $ 0.076 S 2aud
Contribution of operating costs to gas cost 0.069 2
Penalties:
Filter cake ($30/dry ton) 0.055 1.55
Waste water from filter
($1.00/1000 gallons) ; 0.001 0.03
Waste rejected by trommel screen and
air classifier ($3.50/ton) 0.009 0.26
Credits:
Fresh waste ($10.65/ton) (0.102) 2.87
Sewage sludge ($50/dry ton) (0.018) 0.51
Scrap iron ($25/ton) (0.016) 0.46
$ 0.074/m?* $ 2.09/mef
EVALUATION OF THE PROCESS
There can be little doubt that the investigation of fuel gas production from
solid waste is both timely and significant. Fuel gas production from solid
waste appears to offer at least a partial solution to the search for alternative
energy sources, particularly for natural gas. In addition, the technology and
operating experience gained from this process have direct application to
other promising bioconversion concepts.
Process design
The conceptual process design proposed for fuel gas production from solid
waste, Fig.1, does not appear to require the development of any new tech-
nology to construct a commercial-scale facility. On the other hand, an ex-
tensive background of bench- and pilot-scale data which would permit the
247
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confident design and prediction of performance of a full-scale operating
plant is presently unavailable.
The design of the feed preparation system is based upon the current state-
of-the-art of commercially available equipment. Most of the components
selected have had previous application in mineral processing or pulp and
paper manufacture. The mechanical performance and reliability of each
component has been extensively proven in these fields, but application to
solid waste is somewhat limited. For example, production-scale air classifi-
cation of shredded municipal waste has only recently been accomplished. As
more facilities come on-line, additional operating data will become available
which will permit an optimization of the feed preparation system design.
Fifteen major resource recovery plants are expected to be on-line throughout
the United States by 1976 [11]. In addition, numerous publicly and private-
ly funded research projects are underway which should provide valuable
operating data for further optimization of the feed preparation design. How-
ever, few of these projects may be expected to concentrate on the preparation
of a high-purity cellulosic fraction suitable for anaerobic digestion, and none
will examine the interface between the feed preparation and digestion systems.
Many questions remain to be answered with respect to the design of the
backend of the system. The most important question pertains to the maxi-
mum permissible volatile solids loading for the anaerobic digesters. The vola-
tile solids feed concentration and the solids retention time selected by anal-
ysis to produce a minimum gas cost result in a volatile solids loading to the
digesters near the upper limit of that normally encountered in sewage sludge
digesters. None of the experimental data published to date for solid waste
digesters deals with performance under these operating conditions. Discus-
sions with equipment manufacturers indicate that the assumed solids con-
centrations in the digester feed and effluent are also near the upper limit of
that normally handled with the type of equipment proposed for pumping,
mixing and dewatering. As is the case for the feed preparation equipment,
process operating data are currently not available relating to various perfor-
mance characteristics in such a manner as to permit optimization of the pro-
cess. Experiments to date have not been run at a sufficiently large scale to
gather the type of data necessary.
Process ecnomics
The projected economics for the 907 metric ton/day fuel gas from solid
waste facility should be evaluated from two standpoints. First of all, do the
projected economics accurately represent those to be expected from a com-
mercial facility? Secondly, are the projected economics acceptable to the
user community and the gas consumer?
The projected economics are judged to be representative. Capital costs
have been determined from equipment manufacturer’s quotations, from en-
gineering estimates developed by consulting.engineering firms for similar in-
249
stallations, and from published, historical data. Where multiple quotes were
available, capital costs were chosen to represent what was judged to be the
best available equipment from the standpoint of performance. Capital costs,
therefore, tend towards the conservative side. All costs have been escalated to
uniform (June, 1974) construction costs using the Engineering News Record
(ENR) Construction Cost Index. Costs of installation and auxilliary equip-
ment have been included. The American Gas Association public utility cost
accounting structure used considers the associated costs of debt and equity
capital as well as operating costs [9]. It must be emphasized that while the
economics are representative of those realistically expected from a commercial-
scale facility, performance at the levels required has not yet been consistent-
ly demonstrated in the laboratory.
The projected net gas cost is judged to be acceptable. The economic anal-
ysis indicates that, under baseline operating conditions, the net cost of gas
will be in the range of $0.028 to $0.097/m? ($0.75—$2.75/mcf), depending
upon the ownership option selected for the plant and the cost of debt and
equity capital. Based upon figures published in the latest edition of Brown’s
Directory of North American Gas Companies, the average revenue for inter-
state gas sales was $0.028/m? ($0.75/mcf)[12]. At that time, the average
price paid producers was $0.007/m? ($0.21/mcf) at the well head. The
Federal Power Commission (FPC) has proposed an increase to $0.009/m?
($0.245/mcf) for ‘“‘old” gas [13]. ““New”’ gas, from wells commenced on or
after January 1, 1973, has recently been priced at $0.018/m? ($0.50/mcf)
by the FPC, with annual increases of $0.0035/m? ($0.01/mcf) allowed [14].
Intrastate gas sales, which are not regulated by the FPC, have reached
$0.057/m? ($1.60/mcf) or more [15]. Prices for other supplemental sources
of natural gas are even higher. Imported natural gas from British Columbia
is presently set at $0.035/m? ($1.00/mcf) with annual. $0.007/m? ($0.20/mcf)
increases set for each of the next three years [16]. Imported liquefied natural
gas from Algeria is estimated to have a landed cost of $0.07/m? ($2.00/mcf)
[17]. Synthetic natural gas from naphtha and coal is estimated at $0.070—
$0.088/m? ($2.00—$2.50/mcf)[18]. To each of these prices, an increment
equivalent to the pipeline transmission cost must be added to yield a cost
equivalent to the bioconversion process.
An appropriate comparison may be made with other energy sources. A
study conducted by the FPC showed that steam electric generating plants were
paying $0.412/G J ($0.436/MM Btu) for natural gas, $0.61/G J ($0.64/MM
Btu) for coal and $0.76/G J ($1.87/MM Btu) for oil, based on April 1974
prices [19]. A further evaluation of current oil prices is revealing. ‘“Old”’
oil is priced by the Federal Energy Administration at $4.25/bbl (1 bbl = 159
liters), or $0.825/GJ ($0.875/MM Btu) [20]. ‘““New’’ domestic oil may fol-
_ low the market and is priced at $10—12/bbl. Imported crude oil from the
Middle East is currently priced at $11.63/bbl and crude from Venezuela is
priced at $14.43/bbl [13]. Methane produced from solid waste appears to
be competitive with these prices. The gas produced from a privately owned
250
and financed fuel gas from solid waste facility at $0.075/m? ($2.09/mcf) has
an energy equivalent price of approximately $11.00/bbl of crude oil.
Potential impact
The potential for a process which converts refuse to methane is significant.
Residential and commercial refuse is produced at a rate of 1.4—2.3 kg
(8—5 lb.) per person per day. At 4 lb./person/day, a 907 metric ton/day
facility would service a population of approximately 500,000 people. Ac-
cording to the 1970 U.S. Census, there were 26 cities in the country with
populations in excess of 500,000. More significantly, there are 65 Standard
Metropolitan Statistical Areas (SMSA’s) in the U.S. with populations in ex-
cess of 500,000. The aggregate population of these SMSA’s is in excess of q
100,000,000 — half of the nation’s population. In terms of a 907 metric ton/day}
solid waste to methane facility, there is a potential market for over 200 plants |
in the urban areas of the United States.
A 907 metric ton/day bioconversion facility will produce approximately
105,000 m? (3.7 million ft.° ) of methane per day, or 0.21 m?(7.4 ft.? ) of
methane per person. The 65 SMSA’s with populations in excess of 500,000
have a potential for gas production from waste in excess of 21,225,000 m°
(750,000,000 ft.° ) per day. Based on published figures [21], this process, if
implemented in these 65 SMSA’s, could produce approximately 1.5% of the
total natural gas consumed in the United States. In order to identify further
those regions of the country in which fuel gas production from solid waste
could have significant impact, this study has been extended to each of these
major SMSA’s. The population of each was determined from the latest U.S.
Census (1970). Potential gas production from each SMSA was determined
based on an average daily production of 0.21 m? of methane per person. Ac-
tual gas consumption in each SMSA was estimated based upon figures
published in Brown’s Directory of North American Gas Companies [22]. Be-
cause gas-consumption figures were not usually broken down by SMSA, |
estimates were developed based upon the ratio of customers within the SMSA |
to the total number of customers served by each gas company within the
SMSA. On average, approximately 9 percent of the gas consumed in these
SMSA’s could potentially be produced by the municipal solid waste generated §
by their residents. The median ratio of potential production to estimated
consumption was 4 percent. A geographic evaluation of these results shows |
that these plants would have the greatest impact along the Boston-Washington |
corridor, an area highly dependent upon imported energy (Fig.2).
Figure 3 depicts the dramatic need for the additional fuel gas which could
be produced from solid waste. Interstate pipeline curtailments for firm con-
tract gas have been estimated for the five winter months — November, 1974
to March, 1975 — by the Federal Power Commission and the American Gas
Association. The potential gas production from these 65 major SMSA’s
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251
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253
TABLE 2
Experimental matrix — program priorities
Necessary to Necessary Priority
prove concept to prepare rank
Tinayiekt See un oo eotulleseale
Technical Economics design
Feed preparation
Demonstrate capability to provide required x x x 9
digester feed
Determine sequence of operations x 13
Determine primary shredder output size x x 15
Determine secondary shredder output size x x 16
Determine trommel screen opening x x 14
Confirm separation efficiencies X x 10
Establish character of daily and seasonal x x LT,
variations
Determine properties of residual materials x x 19
Digestion
Confirm and demonstrate digester performance X x x 1
Obtain continuous operating data at highest
possible total volatile solids feed x xX Wk
Demonstrate effective digester performance x x x 2
when solids retention time is optimized
with respect to over-all process efficiency
Evaluate thermophilic and mesophilic modes xX x Xx 6
of operation
Evaluate effect of particle size on digester x Xx 12
performance
Evaluate effect of mixing power and mode x x x a
on digester performance ~
Evaluate effect of filtrate recycle on x X x 8
digester performance
Evaluate effect of solids recycle on x x 20
digester performance
Evaluate effect of various sewage sludge/ x x 18
solid waste ratios
Dewatering and residual materials disposal
Evaluate suitability of alternative dewatering xX x xX 3
equipment over range of potential operating
conditions
Evaluate cake produced by alternative x x x 4
dewatering equipment for different dis-
posal schemes
Evaluate the filtrate produced by alternative xX X x a)
dewatering equipment for different disposal
schemes
254
during these months is equivalent to 12 percent of the projected curtailment.
Over a full 12 months, fuel gas production from solid waste in the major
SMSA’s could provide almost 30 percent of the projected national curtail-
ment of interstate gas supplies.
Necessity for further work
A proof-of-concept experimental program has been developed to fill in
the gaps of knowledge in order to permit a confident design of a full-scale
processing facility for the production of fuel gas from solid waste. Table 2
has been prepared as a guide to the relative priorities of various elements of
the experimental program. Each experiment has been classified with respect
to its significance in proving the technical and economic feasibility of fuel
gas production from solid waste and the necessity to conduct the experi-
ment in order to prepare the full-scale facility design.
In January, 1975, the methane production from solid waste program was
transfered to the Energy Research and Development Administration (ERDA).
ERDA has recently announced that a 45,000—90,000 kg/day (50—100 tpd)
experimental facility will be constructed in Pompano Beach, Florida to
prove the concept of methane production from urban waste.
CONCLUSIONS
The above projections show that methane produced from municipal waste
can have significant impact as a supplemental source of pipeline quality gas.
The conclusions come at a time when energy shortfalls and rising costs of
refuse disposal are forcing many major communities to reevaluate their refuse
disposal practices. Anaerobic digestion of the organic portion of municipal
refuse is presently the only known process which will return the energy value
of refuse in the form of pipeline-quality gas.
|
|
ACKNOWLEDGEMENTS
The assistance of Ms. Lynne C. Anderson in developing the economic model
and sensitivity analysis and Mr. David H. Walker in preparing the performance
and cost data is gratefully acknowledged. Mr. Ralph L. Wentworth has provided |
over-all management and technical direction of this program since its incep- |
tion at Dynatech R/D Company.
This work was carried out under National Science Foundation Contract
C-827. The cooperation of Dr. Richard H. Bogan, Program Manager and Dr.
Lloyd O. Herwig, Director, Advanced Solar Energy Research and Technology
of NSF/RANN, is appreciated. We also wish to acknowledge the support of
Consolidated Natural Gas Service Company, Inc., and especially to give recog-
nition to the assistance of Dr. Robert C. Weast, Vice President, Research, and
Mr. Howard W. Scott, Research Engineer.
255
REFERENCES
1
Wise, D.L., Sadek, S.E. and Kispert, R.G., 1974. Fuel Gas Production from Solid
Waste. Progress Report NSF/RANN/SE/C-827/PR/73/4, Dynatech R/D Company,
Cambridge, Mass., Rpt. No. 1151.
Kispert, R.G., Anderson, L.C., Walker, D.H., Sadek, S.E. and Wise, D.L., 1974. Fuel
Gas Production from Solid Waste. Progress Report NSF/RANN/SE/C-827/PR/74/2,
Dynatech R/D Company, Cambridge, Mass. Rpt. No. 1207.
Wise, D.L., Sadek, S.E., Wentworth, R.L. and Kispert, R.G., 1973. Fuel Gas Produc-
tion from Solid Waste. Progress Report NSF/RANN/SE/C-827/PR/73/3, Dynatech
R/D Company, Cambridge, Mass., Rpt. No. 1127.
Pfeffer, J.T., 1973. Reclamation of Energy from Organic Refuse. Final Report Grant
No. EPA-R-08876, Dept. of Civil Engr., Univ. of Ill., Urbana.
Pfeffer, J.T. and Liebman, J.C., 1973. Biological Conversion of Organic Refuse to
Methane. Progress Report NSF/RANN/SE/GI-39191/PR/73/4, Dept. of Civil Engr.,
Univ. of Ill., Urbana, Rpt. No. UILU-ENG-73-2022.
Pfeffer, J.T. and Liebman, J.C., 1974. Biological Conversion of Organic Refuse to
Methane. Annual Report NSF/RANN/SE/GI-39191/PR/74/2, Dept. of Civil Engr.,
Univ. of Ill., Urbana, Rpt. No. UILU-ENG-74-2019.
Kispert, R.G., Sadek, S.E. and Wise, D.L., 1975. An economic analysis of fuel gas
production from solid waste, Resource Recovery and Conservation, 1: 95.
Cooney, C.L. and Wise, D.L., 1975. Thermophilic Anaerobic Digestion of Solid
Waste for Fuel Gas Production, to be published.
Kavanagh, J.F., 1961. General Accounting Procedures to be Used for Large Scale
Production of Gas from Coal and Oil Shale, Memorandum, American Gas Association
General Accounting Committee.
J.R. Schomaker, personal communication, 1971.
Anon., 1974. Resource recovery, NCRR Bulletin, 4(4): 8.
Hedin, D.G., Ed., 1974. Brown’s Directory of North American Gas Companies, 88 edn.,
Moore Publishing Co., Deluth, Minn.
Anon., 1974. Energy world news. Pipeline and Gas Journal, 201(12): 102.
Anon., 1975. Newsreel. Pipeline and Gas Journal, 202(1): 1. 3
Anon., 1974. Newsreel. Pipeline and Gas Journal, 201(14): 2.
Anon., 1974. Newsreel. Pipeline and Gas Journal, 201(13): 4.
Hale, D., 1974. Point of view. Pipeline and Gas Journal, 201(12): 6.
W.F. Morse, persona! communication, 1974.
Anon., 1974. Newsreel. Pipeline and Gas Journal, 201(14): 2.
Anon., 1974. Energy management report. Pipeline and Gas Journal, 201(13): 838.
Hedin, D.G., Ed., 1973. Brown’s Directory of North American Gas Companies, 87
edn., Moore Publishing Co., Deluth, Minn.
Hedin, D.G., Ed., 1971. Brown’s Directory of North American Gas Companies, 85 edn.,
Moore Publishing Co., Deluth, Minn.
Resource Recovery and Conservation, 1 (1976) 257—269
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
PRODUCTION OF SINGLE CELL PROTEIN FROM AGRICULTURAL
AND FOOD PROCESSING WASTES*
R.C. RIGHELATO, F.K.E. IMRIE and A.J. VLITOS
Tate & Lyle Ltd., Philip Lyle Memorial Research Laboratory, Reading, RG6 2BX (England)
(Received 19th March 1975)
ABSTRACT
A process has been developed in which carbohydrate wastes are fermented to produce
microbial protein suitable for animal feeds. The process consists of (i) a waste preparation
step, (ii) growth of a filamentous mould in submerged culture at a low pH (iii) recovery of
the mould by filtration (iv) drying and bagging. It is estimated that operating scales as low
as five hundred tons/annum can be made economic if the process can be used for most of
the year and labour costs are low.
INTRODUCTION
| Most crops are grown for only a small part of their bulk, so during harvesting
and processing various parts of the plants are discarded. Part is simply ploughed
back into the land and makes a valuable contribution to the structure and
fertility of the soil. Another part, notably straw and dry leaves, is sometimes
burned on the fields because collection and redistribution is too costly. There
remains, collected at farms and food processing plants, many hundred of
millions of tons per annum of very low value material. Steffgen [1] quoted
400 million tons per annum of solid waste from agricultural and allied in-
dustries for the U.S.A. alone. To this must be added many millions of tons
of BOD in liquid effluents, so for every ton of food produced a similar
quantity of carbohydrate waste is collected and subsequently disposed of,
often by burning or oxidation in effluent treatment plants.
The production of microbial protein from wastes of agricultural industries
has received attention in recent years with two main objectives in view — up-
grading the feed value of solid wastes and removing the BOD from liquid
wastes with a bonus in the form of high protein animal feed supplement.
| These processes face a number of economic and technical problems. The
| economic problems stem from the distribution of agricultural wastes. They
are produced worldwide but in relatively small quantities at individual sites
*Paper presented at the Symposium ‘‘Energy Recovery from Solid Waste’’, March 13—14,
1975.
258
and often for only a small part of the year (Table 1). A processing plant built
to take advantage of a fruit cull, for instance, would have a throughput of at
best a few tens of thousands of tons of fruit, yielding probably less than a
thousand tons of single cell protein (SCP). The factory would be inoperative
TABLE 1
Scale and seasonality of waste production
Papaya Olive Palm oil
Average processing plant waste, t/a dry solids 2,000 300 5,000
Season LOV1 4/12 1itfAg
Estimate of SCP production, t/a 500 100 1,500
for part of the year or would have to operate on a different waste; effluents
from e.g. olive processing plants pose similar problems of low throughput
and seasonality. These factors make for high amortisation costs, so the tech-
nology must be such that the capital cost of plant is minimised for an
economically viable operation. Plants that operate year round and ona
larger scale, such as those that process corn and palm oil, present less of a
problem but still require a simple technology to be commercially viable.
The technical problems of microbial protein production stem from the
chemical composition and physical form of the wastes. In general the solid
organic material is mostly carbohydrate, at least half of which is cellulose
(Table 2). Starches, pectins and sugars form the remainder. If the sugars of
TABLE 2
Composition of agricultural wastes
Bagasse Papaya Palm Potato
oil process
sludge water
Total solids,% 49 13 J a
Carbohydrate % of dry solids 82 80 60 75
Fibre 94 9 30 20
Pectins 0 a NT? NT
Starches 0 NT NT 60
Oligosaccharides and
monosaccharides 4.5 67 NT NT
Protein 0 5 0.4 8
Lipid 0 5 10 NT
Ash OF 6 NT NT
“NT = not tested.
the carbohydrate polymers can be mobilised, they can form the basis of
processes such as recovery of sugars or fermentation for ethanol or single cell
protein production. In recent years Tate & Lyle, along with other groups
[2—6], have developed processes for non-cellulosic carbohydrate mixtures. It
has been our intention to use as simple a technology as possible to enable
application to small quantities of material, particularly in developing countries.
The basis of the processes is the fermentation of the carbohydrate or other
organic materials to yield single cell protein (SCP) or in special circumstances
ethanol plus SCP.
GENERAL FEATURES OF LOW-TECHNOLOGY SCP FERMENTATIONS
The organisms used for simple recovery of biomass from wastes must have
a number of special properties (Table 3) — they must be capable of growth
TABLE 3
Properties of microbes for waste utilisation
Broad substrate specificity
High growth rate
High carbohydrate conversion efficiency
Growth at high temperatures (>35°C)
Growth at extremes of pH
Simple recovery from fermentation
High protein content
Non toxic
on a wide range of carbon sources, preferably simultaneously and they must
have a high efficiency of conversion of the substrate to biomass. The last
point restricts the choice to aerobic microbes, since in anaerobic growth
several times more carbohydrate is consumed to obtain the necessary energy.
The organisms that grow on waste in nature may fulfil these criteria and
could be used for SCP production. However, they present certain drawbacks —
they are usually mixed cultures of a wide range of microbes whose ratios may
vary widely with small changes in waste composition or the physical environ-
ment. Therefore, the organisms may vary seasonally or be influenced by small
upstream process changes, possibly resulting in harvesting problems and con-
siderable variability in the product specification.
An alternative approach is to use a microorganism which has the required
characters grown under conditions that favour its growth against that of other
microbes. Filamentous moulds have been used because they can be harvested
easily by filtration and some species can be grown at low pH and high tem-
peratures that inhibit the growth of contaminating bacteria and yeasts.
A strain of Aspergillus niger designated M1 has been isolated from naturally
rotting material and found to conform to most of the criteria listed above
[3,4]. More recently, a Fusarium sp. studied in our laboratories has been
260
found to have an unusually high protein content. Both species grow on a wide
range of carbohydrate-containing substrates (Table 4). Glucose, the most
common constituent of carbohydrates, is rapidly assimilated by most mi-
crobes. The glucose dimer maltose and the polymer amylose were almost as
TABLE 4
Growth of Aspergillus niger (M1) and Fusarium sp. (M4) on single carbon sources
The carbon source was added at 2 g/] to an inorganic salts agar medium in petri-dishes.
The plates were inoculated with a small amount of mycelium and conidia. +, growth;
—, no growth
Substrate M1 M4
Glucose + +
Maltose + ==
Lactose = ="
Cellulose (Whatman Cellulose powder CC41) — -
Rhamnose + +
Cellobiose + +
Xylose + +
Glycerol + +
Pullulan + +
Galacturonic acid + +
Soya oil — i
Pectin (apple) + #
Glutamic acid = +
Casein + +
Acetic acid — =
None po wi
readily utilized by both the Aspergillus and the Fusarium. Growth on
pullulan indicates the ability to cleave the a(1—6) glycosidic links that form
the branch points in starches. Pectin is a polygalacturonic acid present in
many fruits and pectinolytic activity was found in both strains. However,
neither were able to use cellulose as the carbon source. Amino acids, proteins
and lipids which are present in small amounts in most biological waste mate-
rials were used by the Fusarium. Clearly these mould strains, whose natural
habitat is rotting fruit, etc., have a very broad substrate specificity. In nature
substrates are normally found in complex mixtures which may also contain
compounds inhibitory to microbial growth. Growth tests using a wide range
of waste materials showed that in most cases the moulds grow well (Table 5).
Having established that the moulds were capable of growth on a wide range
of substrates, fermentation conditions were devised under which high yields
of protein could be obtained. The carbohydrate conversion efficiencies and
the growth rates were measured in 5 1 batch cultures in aseptic laboratory
261
TABLE 5
Growth of two moulds on agricultural wastes?
Scoring refers to a combination of colony radial growth rate and density on agar plates
Substrate A. niger (M1) Fusarium sp. (M4)
Carob extract ++ ++
Sulphite waste liquor + NT
Molasses cats ++
Olive blackwater ++ ++
Cassava flour NT ++
Papaya slurry tt Tot
Citrus waste te +
++ good growth; + poor growth; — no growth; NT not tested.
fermenters. Oxygen was supplied in excess as measured by in situ membrane
electrode, i.e. the oxygen concentration was greater than 2 X 10* Pa. The pH
was controlled to + 0.2 unit by automatic addition of sodium hydroxide or
hydrochloric acid. Temperature was controlled to within 0.5°C of the set
value. The basal salts medium contained (g/l), (NH4).SO.,, 7.0; NaH,POu,, 2.0;
MgSO, °7H,0O, 0.3; CaCl, -6H,0O, 0.3; KCl, 0.1; Zn Cl,, 0.2; FeSO, -°7H,0,
0.005; Difco yeast extract, 2.5.
The pH had little effect on the conversion efficiency or growth rate over
the range 3.0—6.0 (Fig.1). Below pH 4.0, the growth rate fell but the con-
version efficiency was almost unchanged. The ability to grow at pH 2—3 isa
valuable feature, since most saprophytic bacteria and yeasts grow poorly or
not at all at acid pH. Repeated open cultures in the pH range 2—4 have not
shown gross contamination by extraneous microorganisms. Aseptic precau-
tions, which are expensive on a production scale, are therefore unnecessary.
1.0
0.8
pH
Fig. 1. Carbohydrate conversion efficiency (Y) and specific growth rate (u) of Fusarium sp.
(M4) in batch cultures: effect of pH. Carbohydrate: sucrose, 40 g/l; temperature 30°C.
262
The optimum growth temperature for Fusarium sp. (M4) was 35°C (Fig. 2),
growth almost stopping at 40°C at pH 4. At lower pH the growth rate was
higher at 40°C but stopped at 42°C. The ability to grow over a wide range of
temperatures is important since heating and cooling facilities must be avoided
to minimise the cost of fermentation. The conversion efficiencies found here
are close to the maximum growth efficiencies reported for filamentous
moulds [7,8].
1.0
0.8
0.6 .
0.4
0.2
0
0.2
@<
0.1
0
20 25 30 35 40 45
Temperature°C
Fig. 2. Carbohydrate conversion efficiency (Y) and specific growth rate (u) of Fusarium sp.
(M4) in batch cultures: effect of temperature. Carbohydrate: sucrose, 40 g/l; pH 4.0.
The effects of pH and temperature on growth rates and carbohydrate con-
version efficiencies were established in the presence of excess oxygen. The
oxygen demand of rapidly growing cultures of a mould at 10—20 g/l dry
weight is in the range 100—200 mmoles/1/h. To satisfy this demand requires
the use of high-powered aeration and mixing systems. But to install such
systems would be inefficient since the peak oxygen demand occurs for only
a few hours in a batch fermentation cycle of 20 h. Lower power inputs which
would cause oxygen-limitation of growth would extend the fermentation
cycle but would consume less power overall. However, during oxygen-limited
growth, many organisms exhibit mechanisms for gaining energy which give a
low conversion efficiency of carbohydrate to biomass and leave a residue of
organic material in the process water. When the Fusarium sp. (M4) was grown
under oxygen-limited growth conditions the growth rate was lower, but the
oxygen respired and carbohydrate efficiency was unchanged and extracellular _
organic compounds did not accumulate (Table 6). Thus, oxygen-limited growth |
conditions may be used to control the rate of growth and to save power costs.
The product of this fermentation is a mass of fine filaments, or hyphae,
which make up the fungal mycelium. The crude protein content of the dry
mycelium was in the range 25—85 percent for A. niger (M1) and 41—51 per-
cent for Fusarium sp. (M4). The actual protein content calculated from the
amino acid composition was 70 percent of the crude protein for A. niger (M1)
and from 80 to 90 percent of the crude protein for Fusarium sp. (M4). The
263
TABLE 6
Effect of oxygen-limitation of growth on carbohydrate conversion efficiency of Fusarium
sp. (M4)
Inoculum, 2 g biomass/1; pH 4.0; temperature 35°C; 40 g/l sucrose.
Oxygen excess Oxygen-limited
Maximum O, transfer rate, 0.100 0.025
mole/1/h
Oxygen consumed, 0.56 0.53
moles/1
Biomass produced, iy 16.3
g/l
Carbohydrate yield constant 0.43 0.41
Time to reach max. biomass, h. 12 20
amino acid profiles (Figs.3 and 4) are similar to soya meal. Feeding trials with
chickens and pigs have shown the material for strain M1 to be non-toxic. It
was a good substitute for part or all of the soya bean meal in feeds for pigs.
The results of chick growth trials varied with the waste used for the prepara-
tion of the SCP and further tests are to progress to elaborate upon the results.
Aspergillus niger M1. Crude Protein content 31%
16 True ” ” 21/70
Ml Soya bean meal .
g/16g N.
Fig. 3. Amino acid content of mycelium.
18 Fusarium M4. Crude Protein content 47%
16 True» ” 46%
Gl Soya bean meal
g/16g N.
Met Cys Lys Arg ile Leu PA. Tyr Thr Val His Ala Glu Gly Pro Ser Asp
Fig. 4. Amino acid content of mycelium.
264
PROCESS DESCRIPTION
Waste materials suitable for the growth of the microbes described above
can be classified broadly into two categories. These are the solid or semi-solid
wastes such as spoiled fruit, carob pods, date waste and molasses, and low con-
centration wastes which are usually pollution hazards, such as olive and palm
oil process water, corn steep water and canning wastewater. Carob pods and
spoiled papaya have been studied in our laboratories (Table 7). The carob tree
is found in the Mediterranean countries. Its bean is collected for a valuable
gum. The pod has a high sucrose content and has long been used in cottage
industries for making syrup and sweets. The papaya is a soft-fleshed tropical
fruit which has a substantial local consumption and is also packed for ex-
pensive markets in the U.S.A. and Carribean.
TABLE 7
Analysis of carob and papaya waste
Waste Carob pod Papaya cull
% dry matter 70 13
Composition % of dry matter
Fibre eee) 9
Sugars 54.9 67
Pectin = i
Protein 4.5 5
Lipid 0.5 =
Ash 3.0 6
kg dry SCP production per ton
fresh waste 250 60
A waste such as papaya cullage may be slurried with water or in the case of
the carob pod a hot water extract may be made. The concentration is adjusted
to give approximately 4 percent fermentable carbohydrate and the medium is
fermented to give approximately 2 percent fungal biomass. Slurrying and fer-
menting the entire waste results in an increase in protein content of dry mate-
rial of from 15 to 25 percent. If an extract of fermentable carbohydrates is
made, the dry product contains from 30 to 50 percent protein, depending
upon the fungus used.
The simplest apparatus for treatment of solid wastes consists of a tank in
which the slurry or extract is prepared, a fermenter equipped with a stirrer
and an air compressor, and a rotary vacuum filter. The total power consump-
tion is about 1.0 kwh/kg biomass at 25 percent solids. A plant of this type will
be installed in Belize in the near future. It will produce about 100 ton/year of
single cell protein from a variety of waste materials. For plants much larger
than 100 ton/year, a cooling system is required to remove the heat of fermen-
ee
tation. If possible, the wet cake should be fed, after pasteurisation, directly
to animals, thereby avoiding the expensive drying step. If dried, the material
can be bagged and is stable for months.
Microbiologically, the process is a simple batch fermentation. The waste is
prepared and a small quantity of diammonium phosphate, or other ammo-
nium salt, is added to give sufficient anions to produce a low pH as the am-
monium ion is assimilated. The fermenter is inoculated with a large number
of spores of the mould which germinate and grow as long branched filaments.
During growth the pH falls rapidly and the growth of contaminant microbes
is inhibited. After about 20 h the fermentable carbohydrate is exhausted and
growth stops. About 90 percent of the culture is harvested by filtration and
the remaining 10 percent is left as inoculum for the next batch of medium.
The capital cost of equipment is low, $56,000 for the smallest plant en-
visaged, 100 ton/year (Table 8). However, the operating costs per ton of
product are high on such a small scale (Table 9). In this example, the cost of
TABLE 8
Microbial protein production from solid agricultural waste — Capital costs
SCP production (300 day operation) 100 ton/year 500 ton/year
$ 000 $ 000
Material preparation 7 Uy
Fermenter 5 14
Aeration 6 16
Cooling = 6
Filtration 11 Al
Water filters 2 9
Installation 9 23
Buildings 5 14
Dryer 10 30
Total 56 165
TABLE 9
Microbial protein production from solid agricultural waste — Operating costs
SCP production (300 day operation) 100 ton/year 500 ton/year
$ 000 $ 000
Raw materials 2.7 13
Power (150 MWh/700 MWh) 3.0 15
Labour 20.0 30
Direct cost yaaa | 58
Amortisation (10 year) 5.6 16.5
Finance (10% interest ) 5.6 16.5
Total 36.9 93
Unit cost $ 369/ton $ 188/ton
266
skilled labour in Belize, and an arbitrarily chosen 10 year amortisation
period were used. The process could be economic on the 100 ton/year scale
only in countries with cheap labour since labour contributes over half of the
cost. As the scale of operation is increased, the unit price decreases.
The treatment of watery effluents from agricultural processing plants
differs in several respects from that of solid wastes. Effluents are often pro-
duced 24 hours per day and for much of the year. The concentration of sub-
strates for fermentation is low — no more than 25 g/1 for palm oil process
water and more normally less than 5 g/l for wastes from the canning industry
and from starch processing (Table 10). In these cases, the reduction of the
TABLE 10
Analysis of potato and palm oil process effluents
Potato Palm oil
process process
water? water
Solids, % 0.7 5.0
Carbohydrate, % dry solids 80 60
Fibre 20 30
Pectin + +
Reducing sugars reser +
Starches 60 N.T.
Protein 8 0.4
Lipid + 10
Ash <10 ca. 5
BOD., mg/1 400 22000 |
Volume of effluent 80 m?/h 20 m*/h
Potential SCP production 180 ton/year ca. 3000 ton/year
*+ present as minor component; NT not tested.
biological oxygen demand (BOD) may be more important than the produc-
tion of SCP. At least three fungal processes are already in operation for simul-
taneous BOD reduction and SCP production. The ‘“‘“Symba”’ process using an
Endomycopsis to hydrolyse starch in wastes followed by yeast growth on the
sugar was developed in Sweden many years ago [6]. The Pekilo process for
starch wastes and sulphite waste liquor uses conventional aseptic continuous
culture in stirred fermenters [5]. The lagooning process described by Church
et al. [2] for corn processing wastes is reported to have turned effluent treat-
ment into a profitable operation. Work in our own laboratories, and in con-
junction with Dr. R.N. Greenshields at Aston University, has centred on the
use of unstirred tower fermenters [9]. The process water, after addition of
inorganic salts, is percolated up a column-shaped fermenter. Aeration is
accomplished by sparging air through a perforated base plate. The mould
grows in this column and is retained in the fermenter by means of a stagnant
zone at the top which causes the mycelium to settle back into the fermenter
whilst the water flows off. Thus, high concentrations of mould are held in
the fermenter to permit rapid processing of the waste in relatively low fer-
menter capacities. The form of the mycelium is important in such fermenters;:
it must be as tightly-branched tiny pellets, giving a macroscopic appearance
of sandgrains, to enable efficient aeration and sedimentation. In other aspects
the process is similar to that for solid wastes. Costings made on the basis of
a very high BOD material — palm oil waste from a typical factory — show the
process to have a capital cost of less than $250,000 for a plant processing
over 500 m?/day (Table 11). The process appears to be profitable using U.K.
labour costs when the product is sold at the U.K. soya meal price (Table 12).
TABLE 11
Microbial protein production from process effluents — Capital cost
$ 000
Fermenters, 4 X 10 m? 55
Air compressor, 20 m?/min 18
Filtration 46
Dryer and bagger 60
Installation 30
Buildings 25
Total 234
Land area required approx. 280 m?; Effluent: 20 m?/h; 22000 mg/l BOD, ; 300 day/year;
1500 ton/year SCP.
TABLE 12
Microbial protein production from process effluents — Operating cost
$ 000
Raw materials per annum 40
Power (1200 MWh) 24
Labour 125
Direct cost 189
Amottisation (10 years) 23
Finance (10% interest) 23
Total 235
BOD cost 7.4 ct/kg
SCP cost 16.0 ct/kg
SCP sale at U.K. soya price 20.0 ct/kg
Net profit 2.0 ct/kg BOD
268
MASS AND ENERGY BALANCE
It can be argued that in a world with limited material resources, in particular
energy, processes should be subjected to analyses of conservation mass and
energy as well as conventional costing procedures. The process can then be
compared with others which use the same raw material or produce the same
product and an assessment made of its relative efficiency. The practical value
of such analyses depends upon a knowledge of the factor limiting agricultural
productivity, e.g., supply of energy or provision of protein or of calorific
food intake. This value in turn depends on the social and political priorities
set by the community. Here we have made a restricted analysis of the mass
and energy balances for SCP production from wastes without the knowledge
of what limits overall agricultural productivity.
The substrate mass balances for SCP production (Table 13), show that
TABLE 13
Carbon and nitrogen balance
Carbohydrate is Oxygen SCP CoO,
——— 3.1 MJ
1 kg carbon 1.3 kg 0.5 kg carbon ¥ 1.8 kg ss
(NH,),HPO, SCP re Effluent
1kgN 0.9 kgN 0.1 kg N
most of the nitrogen is retained in the product, but half of the carbohydrate
is lost, used for energy for the synthesis of the highly ordered biological
macromolecules. However, if the materials would otherwise be burnt, buried
or discharged to the rivers and seas, the recovery of 50 percent of the carbon
represents a net increase in carbon available to the food system, gained at the
expense of a small quantity of fixed nitrogen. Similarly, a summation of the
energy inputs to the process can be made and compared with the energy con-
tent of the SCP recovered. The power consumption of the plant plus the
energy content of the ammonium salt is the input, equivalent to c 3.5 MJ/kg
dry SCP. The energy recovered as SCP is c 6.4 MJ/kg [10]. Thus, ignoring the
energy tied up as plant and the energy used as manual labour, there is a net
gain of 2.9 MJ/kg.
CONCLUSION
The partial recovery of agricultural wastes as single cell protein could make
a contribution to conservation of the fixed carbon resources produced on the
land. In certain circumstances, wastes can be recovered by commercially
viable processes, particularly where an expensive alternative disposal method
is necessary. Even operating scales as low as a few hundred tons/year can be
made economic if the process can be used for most of the year and labour
costs are low, conditions which can be met in many developing countries.
269
ACKNOWLEDGEMENTS
Our thanks are due to Dr. G.G. Morris and Mr. S.A. Campbell who did
much of the laboratory work on which the processes are based.
REFERENCES
1
2
~1 ©
10
———————
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tenance energy and growth rate on the metabolic activity, morphology and conidiation
of Penicillium chrysogenum. J. Gen. Microbiol., 50: 399.
Carter, B.L.A., Bull, A.T., Pirt, S.J. and Rowley, B.I., 1971. Relationships between
energy substrate utilisation and specific growth rate in Aspergillus nidulans. J. Bacteriol.,
108: 309.
Imrie, F.K.E. and Greenshields, R.N., 1973. The tubular reactor as a simplified fer-
menter. Proceedings of 4th Intl. Conf. in Global Impacts of Applied Microbiology.
Sao Paulo, Brazil, 23rd—28th July.
Prochazka, G.J., Payne, W.J. and Mayberry, W.R., 1973. Calorific contents of micro-
organisms. Biotech. Bioeng., 15: 1007.
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Resource Recovery and Conservation, 1 (1976) 271—277
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
PROBLEMS AND POTENTIAL ASSOCIATED WITH THE PRODUCTION
OF PROTEIN FROM CELLULOSIC WASTES *
CHARLES J. ROGERS
Solid & Hazardous Waste Research Laboratory, United States Environmental Protection
Agency, Cincinnati, Ohio 45268 (U.S.A.)
(Received 15th April 1975)
ABSTRACT
Annually, billions of tons of cellulose are included in agricultural and municipal waste
streams. This cellulose could be the feedstock for biological and chemical conversion to
useful and valuable products. Bioconversion could add to the world’s protein supplies as
well as supply a variety of chemicals. There still remain technical constraints hindering
development of viable bioconversion processes utilizing these wastes. The cellulose is
resistant to rapid assimilation by microorganisms because of its semicrystalline nature.
One way to overcome this resistance is to pre-treat the cellulose photochemically, followed
by a novel acid hydrolysis. Such processing yields a cellulose to glucose conversion of from
40 to 50 percent per pass through the reactor.
INTRODUCTION
The prevalence of poverty and pressure of population growth in various
parts of the world, especially in less developed areas, have made it difficult
to provide many peoples with an adequate nutritional diet, particularly with
respect to protein content. This problem, which may become even more
serious in time, is due, in part, to an inefficient world food distribution sys-
tem, a world shortage of fertilizers and energy, and climatological conditions
that have produced droughts and flooding in many parts of the world. Devel-
opment of technology for the conversion of renewable organic materials
(i.e., agricultural crop residues and the organic fraction from municipal and
industrial waste streams) could potentially have a profound impact on both
fuel and protein shortages throughout the world.
Historically, as early as 1883, Hoppe-Seyler recognized the decomposition
of organic matter under natural conditions [1]. Omelionski [2] pioneered
much of the early work on the fermentation of cellulose by microorganisms
to form gases, fluids, and humus. Many papers and patents have been published
*Paper presented at the Symposium ‘“‘Energy Recovery from Solid Waste”, March 13—14,
1975.
272
on the possibility of producing organic acids, alcohols, and methane through
fermentations of cellulose by microorganisms. Unfortunately, progress over
the last 100 years on the utilization of cellulose as a feedstock has not been
impressive nor has the use of organic waste fulfilled its potential as an inex-
pensive feedstock to produce food and energy products through fermentation
technology.
BIOCONVERSION PROCESSES
Although bioconversion processes have been extensively researched with
some success as a mechanism for utilizing organic waste, there appears to be
a growing, new interest in the process prompted by:
— the recent 300 percent increase in crude oil prices which improves the
competitiveness of processes considered marginal in the past,
— increased freakish weather patterns causing droughts in some parts of
the world and floods in others, resulting in unpredictable annual crop yields,
— costs of food, fertilizer, and fuel that have sharply increased in price,
and
— world food reserves that have now dropped to less than a 30-day supply,
with the United States and Canada no longer having substantial reserve food
stock to respond to world emergencies.
The sources of organic wastes for use in bioconversion processes include
agricultural crop residues, waste paper from domestic refuse, sewage, animal
wastes, paper mill sulfite liquor, and food processing waste.
Technical constraints that hinder development of viable bioconversion
processes
Cellulose is the major constituent of organic feedstocks. It occurs in the
presence of hemicellulose, a related structure, and with lignin, a nonpoly-
saccharide.
The cellulose molecule is a polymer with molecular weight generally in the
range of 600,000 to 1,500,000. Its degree of polymerization (DP) ranges
from approximately 3,000 to 10,000. Glucose, as well as cellobiose, cello-
triose, and cellotetrose, can be isolated when cellulose is hydrolyzed. Com-
plete hydrolysis by acid yields D-(+)-glucose as the only monosaccharide.
Other polysaccharides can also occur in the presence of cellulose. For example, |
cereal straws and bran contain pentosans (most commonly xylan, which is
built up from d-xylose units), which yield pentoses on hydrolysis, rather than
glucose. Starch is present in the majority of plants, and this material is syn-
thesized from glucose units.
Cellulose in organic materials occurs in two forms — the amorphous, which
is susceptible to enzyme and acid hydrolysis, and a much less susceptible
crystalline form. In crystalline or native form, the cellulose molecules are
stabilized laterally by hydrogen bonding between hydroxyl groups of adjacent |
i
273
molecules. Hydrogen bonding and the arrangement of the cellulose molecules
in native cellulose has been described by Liang and Marchessault [3]. An
excellent discussion and bibliography of review articles on this subject is
provided by Ward [4]. He points out that the consequence of the high degree
of order in native cellulose is that not even water molecules, let alone enzymes,
can enter the structure. Consequently, native cellulose is essentially inert in
the biological and chemical processes.
Pretreatment processes
Before agricultural crop residues and other cellulosic solid wastes can ef-
ficiently and economically be used as substrates for bioconversion processes
to produce energy and microbial protein, an inexpensive way must be found
to modify this material so that it can be consumed easily and quickly. A
number of physical and chemical processes with the potential for enhancing
fungal digestion of waste cellulose have been evaluated and reported on in an
earlier publication [5|. The treatment processes evaluated included alkali,
electron irradiation, microwave, laser, viscose, and photodegradation. Al-
though significant structural changes occurred in pretreated cellulosics, these
changes were not translated into dramatic improvements in the conversion
rates of waste to desired products. One of the cellulose pretreatment tech-
niques that appeared promising, inexpensive, and practical for conditioning
large quantities of waste was sensitized photodegradation.
Rader and Schwartz [6] revealed that polysaccharides such as starch and
cellulosic materials, in the presence of a water-soluble metal or nitrogen-base
salt of nitrous or hyponitic acid, are converted to saccharides of lower molec-
ular weight by irradiation with light that is rich in frequencies in the neighbor-
hood of 355 nm. On the basis of this information, Fookson and Frohnsdorff
[7] conducted a study to evaluate the technical and economic feasibility of
using the sensitized photodegradation process to increase the use of waste
cellulose in bioconversion processes.
Cellulose (Eaton-Dikeman cotton linter papers) was irradiated in a reactor
at varying wave lengths and intensities. The optimum NaNO, concentration
required to decrease the degree of polymerization (DP) was determined. The
cotton linter papers were subjected to 0, 0.1, 1.0 and 10 percent NaNO,
additions. The results of this experiment (Fig. 1) suggest, for the 253.7 nm
lamps and within the range of conditions used, that 1 percent by weight
NaNO, could reduce the DP of cellulose containing materials.
Test for fungal growth response
The samples of cellulose treated with NaNO, and irradiated to reduce the
DP were tested for their ability to be utilized by fungi. With reduced DP, in
addition to no significant increase in carboxyl or carbonyl groups, the rate of
cellulose degradation should have increased significantly.
274
1000 |
DEGREE OF POLYMERIZATION, DP
600 No. of
lamps
8
400 16
16
200 8,16
16
TIME, hrs
Fig. 1. Effect of 253.7 nm radiation on NaNo,-treated Eaton-Dikeman cotton linters paper.
One gram of each cellulose sample was placed in 100 ml of a mineral salts
medium and inoculated with a selected fungus as described by Rogers and
Coleman [5]. The reduction of the DP did not improve the digestion rate of
cellulose as expected. Future plans, however, call for studies to determine if
photodegradation can be implemented to improve the yield of glucose by
subsequent high temperature/high pressure acid hydrolysis.
Unlike conventional acid hydrolysis processes, a novel process will be in-
vestigated that brings an acid-treated waste cellulose at ambient temperatures
almost instantaneously to the optimal hydrolysis reaction temperature by |
contact with superheated water or steam. Preliminary data suggest that acom- |
bination of photochemical treatment and this method of acid hydrolysis could |
give a cellulose—glucose conversion of from 40 to 50 percent per pass through»
the reactor [8].
PROTEIN PRODUCTION PROCESS
The basic processing scheme for producing protein from organic waste is
outlined in Fig. 2. After separation from the inorganic materials, the organic
waste is ground and physically or chemically pretreated. For direct use of
cellulose, the pretreatment may involve the use of a swelling agent or hydrol-
ysis to glucose. The feedstock is passed into the fermenter, which contains
the growth nutrients dissolved (containing K, N, P trace elements) in water.
The microbes utilize the carbohydrates and nutrients to produce a biomass
which is recovered as protein (single-cell protein).
Feedstock
Sterilization
Organic
Waste
Grinder
Chem./Physical
Pretreatment
Recovery
Filter |
Unit
Fermenter
Dried
Protein
Product
Liquor to Fermenter
Fig. 2. Conversion of organic material to fungal protein.
Fermentation technology has been advanced to maximize microbial protein
production to the point that a highly instrumented fermenter can be coupled
to a digital computer for control [9]. Using this device, a “‘dose response”’
technique can be used to determine the optimum carbon to nitrogen ratio.
For example, yeast cells (7.5 g/l) were grown to a density of 105 g/l (dry
weight) in 14 hrs fermentation at a growth rate of 7.5 g/l/hr. This is reported
to be the highest yield ever reported for the yeast Candida utilis. The industrial
average is approximately 25 g/l dry weight [9]. Protein yields can further be
increased up to 15 percent by adding compounds such as indole-3-acetic acid
or 2,4-dichlorophenoxyacetic acid in concentrations of parts per million to
the growth media [10].
The production of microbial protein from organic wastes has already been
demonstrated on a small scale; what is lacking is information on the economic
feasibility and future markets for the protein product produced in this
country.
Potential advantages of using microbial production processes
A number of factors weigh heavily in favor of developing microbial protein
production processes to augment conventional protein deficits. Microbial
protein offers the following possible advantages over conventional processes:
276
— Greater feedstock conversion to protein (for cattle, 3.6 kg grain yields
0.453 kg beef on a feed lot; for single cell protein (SCP), 3.6 kg feed
yields 1.45 kg/SCP, dry weight.
— Prevents loss of nutrients such as N, P, K compared to the uncontrollable
loss with conventional farming methods.
— Is not influenced by freakish weather patterns (i.e., flooding, frost,
droughts, etc.). |
— Is produced from renewable resources without interfering with primary
productivity of agricultural land.
— Is less energy intensive than some conventional farming methods [11,12].
USE OF MICROBIAL PROTEIN
Tortula yeast grown on molasses or sulphite liquor has long been used in
food in small quantities, primarily as a vitamin source. There is a limitation
on the amount of microbial protein that can be used directly in human diets
since rapidly growing cells have a high nucleic acid content which man would
convert to uric acid. Too much uric acid may lead to its deposition in joints
where it causes gout, or in the kidneys where it may lead to stone formation.
As an alternative to direct human use of fungal protein, a short-term prelim-
inary trial of feeding fungal protein to rainbow trout was conducted at
Oregon State University Food Science and Technology Laboratory [13]. The
fungal protein was 25 percent of the total diet and fed to young rainbow trout
over a 2 month period. This fungal protein was substituted for fish meal and
the trout grew as well on this diet as they did on the control feed. The feeding
enthusiasm was excellent and the animals exhibited no signs of toxicity.
Presently, more extensive fungal protein feeding studies with chicks are being
conducted at Tennessee State University.
MARKETS AND FUTURE MARKETS VALUE OF SINGLE CELL PROTEIN
Many chemical specialists believe that single cell protein will become a
world commodity [12]. First, it is apt to be included in small tonnages in
specialty markets, such as milk powder replacements. Within 10 years, the
larger commodity class tonnage is likely, if a number of variables in world
protein production — such as soybean price level, weather, international
agricultural and monetary policies and sociological and psychological reactions
to eating microbial protein — permit. The potential market value of various
sources of single cell protein has been given [12].
CONCLUSIONS
The general consensus is that the malnutrition crisis in the world today is
largely a protein shortage [14,15]. Current research and development efforts
to obtain protein by growing microorganisms on hydrocarbon and waste
277
organics should be intensified to help provide protein to millions of people
suffering from starvation.
Because of the chemical and physical properties of cellulosic materials that
slow its microbial conversion to protein, new conceptual approaches should
be researched and developed to improve rates of conclusion and product yields.
Utilizing organic waste in biological systems is greatly simplified if the feed-
stocks are transformed to a more enzymatic active form or are hydrolyzed to
glucose. Until pretreatment technology for cellulose is developed to increase
rates and yields, the prospects of using organic wastes as feedstock in econom-
ically viable fermentation processes are not optimistic.
REFERENCES
1 Hoppe-Seyler, F., 1883. Ber., 16: 122.
2 Omelionski, W., 1902. Centr. Baktriol. Parasitenk, Abt. II, 8: 1938, 225.
3 Liang, C.Y. and Marchessault, R.H., 1959. Infrared spectra of crystalline polysaccharides.
I. Hydrogen bonds in native cellulose. Journal of Polymer Science, 37: 385.
_4 Ward, K., 1969. Symposium on Foods: Carbohydrates and Their Roles. In: H.W. Schultz,
R.J. Chain and R.W. Wrolstead (Eds.), Cellulose. Westport Avi Publishing Company,
Connecticut, p. 55—72.
5 Rogers, C.J. and Coleman, E., 1972. Production of fungal protein from cellulose and
waste cellulosics. Environmental Science and Technology, 6: 715.
6 Rader, C.A. and Schwartz, A.M., 1967. Method of degrading polysaccharides using
light radiation and a water-soluble metal or nitrogen base salt of nitrous or hyponitic
acid. U.S. Patent 3,352,777.
7 Fookson, A. and Frohnsdorff, G., 1973. The nitrite-accelerated photochemical degra-
dation of cellulose as a pretreatment for microbial conversion to protein. EPA-670/2-
73-052. NERC, Cincinnati, Ohio, NTIS No. 222 115.
8 Walter G. Brenner, Senior Research Scientist, New York University, personal commu-
nication.
9 Nyini, L.K. and Krishnaswami, C.S., 1974. Fermentation process analysis modeling
and optimization. New Brunswick Scientific Company, New Brunswick, N.J.
10 Szabo, M., Scarpino, P.V. and Rogers, C., 1975. Effect of auzins and herbicides on
enhancement of protein synthesis in fungi. J. Agr. Food Chem., 23, No. 2.
11 Gunkel, W.W., Cosher, G.L. and Erickson, J.H., 1974. Energy Requirements for New
York State Agriculture (part 1: food production). New York State College of Agri-
culture and Life Sciences, Cornell University, Ithaca, New York.
12 Wolfson Laboratory for Biology of Industry in Conjunction with Peter Ward Associates
(Interplan) Ltd. of Craydon, London (Five Volume Report published Sept. 1974).
13 R.D. Sinnhuber, Oregon State University, Corvallis, Ore., personal communication,
OW.
14 Crossland, J., 1974. Ferment in technology. Environment, 16, No. 10: 17.
15 Scrimshaw, N., 1974. The world-wide confrontation of population and food supply.
Technology Review, p. 18.
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Resource Recovery and Conservation, 1 (1976) 279—294 ae
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
ENZYMATIC HYDROLYSIS OF CELLULOSIC WASTES TO GLUCOSE*
L.A. SPANO, J. MEDEIROS and M. MANDELS
U.S. Army Natick Laboratories, Natick, Mass. 01760 (U.S.A.)
(Received 19th March 1975)
ABSTRACT
Conversion of cellulose to glucose for the production of food, fuel, and chemicals can
be accomplished by acid hydrolysis or by enzymatic processes. Enzyme complexes derived
from the fungus Trichoderma viride have been found effective in the conversion of cellulosic
wastes into glucose syrups. Trichoderma viride, a fungus found in nature, is the only fungus
known that produces a specific enzyme which is capable of reacting with the crystalline
- fraction of the cellulose molecule.
This paper discusses the production and mode of action of the cellulase complex pro-
duced during the growth of Trichoderma viride, and the application of such enzymes for
the conversion of various municipal, agricultural and industrial cellulosic wastes to glucose
sugar. Included in the discussion are process variables, such as substrate pretreatment,
slurry concentration and enzyme activity, as they affect process conversion rates.
Cellulose is the most abundant organic material which can be used as a
source of food, fuel and chemicals. The net world-wide production of cellulose
is estimated at 90,718 Tg (one hundred billion tons) per year. This is approxi-
mately 68.04 kg (150 Ibs.) of cellulose per day for each and every one of the
earth’s 3.9 billion people. The energy to produce this vast quantity of cellulose
comes from the sun and is fixed by photosynthesis.
Since cellulose is the only organic material that is annually replenishable in
very large quantities, ways must be explored to utilize it as a source of energy,
food, or chemicals (Fig. 1). Cellulose can be converted to glucose by either
acid hydrolysis or enzymatic processes [1,2]. The use of enzymes is more ad-
vantageous. When using acid, expensive corrosion-proof equipment is required.
Moreover, the crystalline structure of cellulose makes it resistant to acid, there-
fore the temperature and acid concentrations needed to achieve hydrolysis
also cause decomposition of the resulting sugars. Consequently, the process
must be balanced so that the rate of hydrolysis is high enough to compensate
for decomposition of the desired products. Glucose yields of approximately
50 percent of the weight of cellulose used have been obtained [3]. Waste
cellulose invariably contains impurities which will react with the acid, thereby
producing other unwanted by-products and reversion compounds.
On the other hand, the Natick Development Center has developed an
enzymatic process which is specific for cellulose and does not involve reactions
*Paper presented at the Symposium ‘‘Energy Recovery from Solid Waste”, March 13—14,
1975.
280
Enzyme Hydrolysis
Animal Food = = Human Food
; o
x c - ‘
“ Microbial Conversion
Chemical Single Cell Protein Fuel (Ethanol)
Raw Materials Solvents (Acetone)
Chemical
Antibiotics
Enzymes
Fig. 1. Cellulose — A chemical and energy resource.
with impurities that may be present in the waste. Moreover, reactions take
place under moderate conditions so that the glucose yield is 111 percent of
the weight of cellulose used. The glucose syrups produced enzymatically are
fairly pure and constant in composition. This enzymatic process is based on
the use of the cellulase derived from mutant strains of the fungus Trichoderma
viride. A schematic diagram of this process is shown in Fig. 2. The first step is
the production of the enzyme. This is accomplished by growing the fungus
Trichoderma viride in a culture medium containing shredded cellulose and
various nutrient salts. Following its growth, the fungus culture is filtered and
the solids discarded. The clear straw colored filtrate is the enzyme solution
that is used in the saccharification reactor. Priot to its introduction into the
reactor, the enzyme broth is assayed for cellulase activity and its acidity is
adjusted to a pH of 4.8. Milled cellulose is then introduced into the enzyme
solution and allowed to react with the cellulase to produce glucose sugar.
Note that saccharification takes place at atmospheric pressure and at a temper-
ature of 50°C. The unreacted cellulose and enzyme is recycled back into the
reactor, and the crude glucose syrup is filtered for use in chemical or microbial
fermentation processes to produce chemical feedstocks, single-cell proteins,
fuels, solvents, etc.
The key to this process is production of a high quality cellulase enzyme
complex from Trichoderma viride capable of hydrolyzing insoluble crystalline
cellulose. This enzyme complex consists of two major components, C,; and Cx.
The Cy component consists of exo- and endo-6-1,4-glucanases. These enzymes
281
RECYCLE
ENZYME AND
UNREACTED
CELLULOSE
> 4 FILTER
&
&
REACTOR SYRUP |= ALCOHOL
in % FERMENTATION
4
ENZYME
(BROTH)
GLUCOSE
TRICHODERMA
VIRIDE
MUTANT
Fig. 2. Enzymatic conversion of waste cellulose to glucose sugar.
are very common and they rapidly attack amorphous cellulose or soluble
derivatives such as carboxymethy] cellulose (CMC) producing glucose and
cellobiose.
The C, is an enzyme required along with C,, for the hydrolysis of insoluble
and particularly crystalline cellulose. The action of C,; is not yet clear although
it has been separated from C, and it is a protein [4]. The simplest explanation,
and the one held by E.T. Reese, is that it is a prehydrolytic enzyme, i.e., it
decrystallizes or hydrates cellulose chains so the C,, can catalyze their hydrolysis
to glucose [5].
C, enzymes are fairly common but C,; enzymes are quite rare. The best
source known is Trichoderma viride [4]. When considering large-scale hydrol-
ysis of cellulose, C, is the limiting factor, consequently, it is essential to use
cellulases containing both C, and C, for effective saccharification. Most com-
with only traces of C,. The cellulase produced by Trichoderma viride is rich
in C, and endo-$-1,4-glucanase. It also contains lower levels of exo-6-1,4-
glucanase and £-glucosidase.
For twenty years, extensive studies of Trichoderma viride and its enzyme
have been made at the Natick Development Center in connection with the
prevention of deterioration of cellulosic materials. The conditions needed to
produce the enzyme in quantity have been defined, and mutant strains have
been developed that produce 2 to 4 times as much cellulase as the wild strain.
It is believed that the upper limit has not yet been reached.
As indicated earlier, the insolubility and crystallinity of pure cellulose and
the presence of lignin in waste cellulose make it a most resistant substrate.
The most satisfactory pretreatment found is ball milling. This reduces the
crystallinity and particle size of the cellulose [4], and increases its bulk density,
making it more reactive for saccharification.
282
mercial cellulases are obtained from Aspergillus niger and contain chiefly C,
j
}
METHODS
Methods used in this paper are described in ref. 4. The Filter Paper Cellulase
Unit equals micromoles of glucose produced per minute from 50 mg of What-
man No. 1 paper incubated with cellulase at a pH of 4.8 at 50°C for one hour,
and is based on the enzyme dilution to give 2.0 mg of reducing sugar as glucose.
The CMC (Cx) cellulase unit equals micromoles of glucose produced per minute
when the enzyme is incubated with 0.5% carboxymethy] cellulose (D.S. 0.50
manufactured by Hercules Powder Co.) at a pH of 4.8 at 50°C for 30 minutes,
and is based on the enzyme dilution to give 0.05 mg of glucose.
EXPERIMENTAL RESULTS
Pestalotiopsis westerdijkii QM 381 (PW) produces a cellulase containing
largely Cy [4]. Consequently, culture filtrates from this organism can hydrolyze
only the amorphous or available portions of the cellulose. Figure 3 shows
several substrates which have been hydrolyzed by broth containing C,.. From
Fig. 3 the information shown in Table 1 is obtained. The data in Table 1
show the positive effect that ball milling has on increasing cellulase activity.
When these same substrates were hydrolyzed by the cellulase broth con-
taining C, and C, produced by Trichoderma viride QM 9414 (TV), the avail-
able or amorphous portion of the cellulose was hydrolyzed very rapidly [4].
Hydrolysis of the crystalline region followed at a less rapid rate. From Fig. 4
the information in Table 2 is obtained.
Total hydrolysis in 48 hours ranged from about 6 percent for fibrous cotton |
to over 90 percent for milled pulp, Sweco 270 [6]. Milled newspaper was 70
percent hydrolyzed. Since newspaper is 30 percent lignin [4], the 70 percent
hydrolysis represents total hydrolysis of the cellulose content of the news-
paper [4]. It is thus apparent that the rate and extent of hydrolysis depends
283
both on the quality of the enzyme used, and the nature and the pretreatment
of the substrate.
More conclusive evidence as to the significant effect C, has on the hydrol-
ysis reaction is shown in Fig. 5. Using filter paper as the substrate and enzyme
solutions with equal C, activity as adjusted on carboxymethyl cellulose (CMC),
NP-M 9425
__—— ~ Sweco 270
Oo ote
12 <
BW2
Cotton-M ieee
2
Glucose mg/ml
% Saccharification
24
/ TIME in HOURS 50°
Fig. 3. Hydrolysis of insoluble cellulose by a C,, cellulase from Pestalotiopsis westerdijkii.
(co) Newspaper, ground in a Sweco ball mill; (4) pure cellulose pulp, ground to 270 mesh in
a Sweco ball mill; (=) ball milled absorbent cotton; (4) BW 200, a ball milled pulp prepared
from SW40, 200 mesh, Brown Co., Berlin, N.H.; (©) Whatman No. 1 filter paper; (4) Avicel,
microcrystalline cellulose, American Viscose Co.; (¢) NEP 40, hammer milled uninked
newsprint, 40 mesh; (4) SW40, hammer milled sulfite pulp, 40 mesh; (2) absorbent cotton,
fibrous.
TABLE 1
Substrate Available cellulose Saccharification
after 1 hour (%) after 48 hours (%)
Absorbent cotton, fibrous 0.7 1.3
Pure cellulose pulp SW 40 1.6 ead
Hammer milled newsprint NEP 40 2.5 6.5
Whatman No. 1 filter paper 2.9 12
Avicel pH 105, microcrystalline 3.8 6.8
cellulose
Ball milled absorbent cotton 4.7 10.6
Ball milled pure cellulose pulp 3.8 11.5
— BW 200
Pure cellulose pulp Sweco 270 10.4 23.8
Ball milled newspaper NP-M 10.4 24.9
284
Sweco 270, ~ +
a
a
ae a
a
Glucose mg/ml
% Saccharification
Fig. 4. Hydrolysis of insoluble cellulose by a complete cellulase from Trichoderma viride.
(co) Newspaper, ground in a Sweco ball mill; (4) pure cellulose pulp, ground to 270 mesh
in a Sweco ball mill; (=) ball milled absorbent cotton; (4) BW 200, a ball milled pulp
prepared from SW40, 200 mesh, Brown Co., Berlin, N.H.;( ) Whatman No. 1 filter paper; (a)
Avicel, microcrystalline cellulose, American Viscose Co.; (¢) NEP 40, hammer milled
uninked newsprint, 40 mesh; (4) SW40, hammer milled sulfite pulp, 40 mesh; (°c) absorbent
cotton, fibrous.
TABLE 2
Substrate Available cellulose Saccharification
after 1 hour (%) after 48 hours (%)
Absorbent cotton, fibrous 1.4 6.0
Pure cellulose pulp SW 40 4.7 37.4
Hammer milled newsprint NEP 40 _ 6.8 28.8
Whatman No. 1 filter paper Oh 59.4
Avicel pH 105, microcrystalline 7.0 39.6
cellulose
Ball milled absorbent cotton 13.5 54.9
Ball milled pure cellulose pulp 12.6 62.1
BW 200
Pure cellulose pulp Sweco 270 23.4 91.8
Ball milled newspaper NP-M 18.0 70.0
285
3.0
Glucose - mg
i)
re)
TIME in HOURS
Fig. 5. Hydrolysis of filter paper by cellulase preparations from Trichoderma viride and
Pestalotiopsis westerdijkii adjusted to equal activities on carboxy methyl cellulose (19 C,
units/ml). (4) Tv QM 9123 culture filtrate; (°c) Tv QM 9414 culture filtrate; (4) Pw QM
381 culture filtrate.
the concentration of glucose produced as a function of time was determined.
The results show that the enzyme solution containing both C, and C, pro-
duced 5 to 6 times more glucose than the enzyme solution containing only the
C,. component. The C, (PW) enzyme rapidly hydrolyzes the limited amorphous
portion of the substrate, after which the hydrolysis stops since it cannot attack
the crystalline portion of the substrate. The C; + C, (TV) cellulase attacks the
amorphous portion rapidly and then continues to hydrolyze the crystalline
cellulose at a slower rate.
Table 3 shows the hydrolysis of a number of pure and waste celluloses by
the culture filtrate of Trichoderma viride. Saccharification is slow for crystalline
cellulose such as cotton, untreated rice hulls or bagasse but milling will greatly
increase their reactivity. Shredded or milled papers also make good substrates.
The fiber fraction separated by the Black-Clawson hydropulping operation of
municipal trash [4] is an excellent substrate material, especially after milling.
The same is true for the shredded cellulose fraction of municipal trash which
is separated by air classification, using the Bureau of Mines resources recovery
process [4]. Waste cellulose from municipal trash is of particular interest
because such waste will be increasingly available in large quantity.
Pretreatment of the substrate is an important variable which will affect not
only the degree of saccharification, but also the economics of the process.
Using newspaper as a model substrate, various substrate treatments were tried.
The results are shown in Table 4. It should be noted from these studies that
milling the substrate gave the best results.
286
TABLE 3
Hydrolysis of cellulose by Trichoderma viride cellulase
Substrate % Saccharification
1 hr 4 hr 24hr 48hr
Pure cellulose
Cotton — fibrous 7 1 Qe 6 10
Cotton — pot milled 14 26 49 55
Cellulose pulp SW40 5 13 26 37
Milled pulp Sweco 270 23 44 74 o2
Waste cellulose
Bagasse 1 3 6 6
Bagasse — pot milled 14 29 42 48
Corrugated fibreboard Mighty Mac 11 DAT 43 55
Corrugated fibreboard pot milled 17 38 66 78
Black Clawson fibers oy 1a 32 36
Black Clawson pot milled 13 28 53 56
Bureau of Mines cellulose a 16 25 30
Bureau Mines pot milled 13 31 43 57
TABLE 4
Pretreatment of newspaper
% Saccharification
1 hr 4 hr 24 hr 48 hr
Boiled in water 4 9 zal 26
Cuprammonium 18 35 52 58
Fitzpatrick (hammer mill) 10 16 25 28
Gaulin (colloid mill) 9 dey PATI 31
Granulator-comminutor 96 14 24 26
Jay Bee-paper shredder 6 12 24 yal
Majac (jet pulverizer) 11 15 26 29
Mighty Mac-Mulcher 10 24 31 42
Pot mill 18 49 65 70
Soaked in water 7 13 24 28
Sweco mill 16 32 48 56
Treated 2% NaOH 8 14 28 35
Viscose 15 30 44 51
i
Because of its specificity, the cellulase enzyme reacts solely with the cellulose |
and does not react with other materials or impurities present in the waste.
Table 5 shows the results achieved with milled newspaper digested in a stirred
tank reactor. Glucose syrups of 2 to 10 percent concentrations were obtained.
The ink, lignin, and other impurities present did not cause any problems [7].
ee _
287
TABLE 5
Hydrolysis of milled newspaper in stirred reactors
Reactor volume 1 liter, stirred 60 rpm, pH 4.8.
Enzyme Newspaper Temp Glucose Saccharification
protein (%) (°C) (%)
(mg/ml) 1 hr 4 hr 24 hr 48hr
(%) (%) (%) (%)
0.7 5 50 0 2.0 2.8 a 50
0.7 5 50 1.0 2.0 As) = 42
1.0 10 50 Diadk 3.1 5:5 hes 66
1.6 10 45 2.0 3.6 5.4 6.5 59
1.6 10 50 223 4.2 6.4 6.3 57
0.8 15 45 ss) 2.8 5.3 (ed 46
0.8 15 50 0.8 2.8 6.1 6.3 38
1.8 10) 50 3.2 6.0 8.6 10.0 60
The residue after hydrolysis was a black sticky material that dried to a hard
nonwettable cake. This material is chiefly lignin which can be burned as a fuel
or\used as a source of chemicals [4].
Results achieved with newspaper show that it is technically feasible to
produce glucose syrups in good yield (40—50 percent) and at a practical rate
from waste cellulose. Newspapers were selected as the model substrate since
such waste is representative of most cellulosic waste present in municipal trash.
In addition to those wastes shown in Table 38, several other industrial and
agricultural wastes have been evaluated and classified as potential substrates
for hydrolysis [7]. Using ball milled newspaper as representative of all wastes
that could be used in the process, the degree of saccharification of other wastes
tested relative to ball milled newspapers are listed in Tables 6 and 7. Substrates
whose relative value is 1.0 or better are considered good substrates for hydroly-
sis.
Milling of the substrate to reduce its crystallinity is an energy-intensive and
costly process. Consequently, an intensive search for other physical, chemical
or combinations of both treatments must be explored to optimize the econom-
ics of the overall process.
A potential approach to reducing the cost of substrate pretreatment may be
the substitution of other pulp refining methods for the ball milling operation.
Preliminary studies with pulped government documents show that pulping
may be very effective as a substrate pretreatment. Saccharification studies
using hydropulped substrates at three cellulose slurry concentrations and at
three enzyme activity levels were conducted, and the results are shown in
Table 8. The weight of glucose and percent saccharification realized as a func-
288
TABLE 6
Wastes for conversion
Saccharified at 50°C, pH 4.8, with T. viride QM 9414 cellulase 1.2 units/ml.
Substrate Relative % saccharification 24 hours?
5%
dry wt. As rec’d As rec’d Ball
wet dry milled
Pure
Cotton = 0.1 0.9
Filter paper aa 0.8 a.
Cellulose pulp = 0.5 1.4
Agricultural
Rice hulls == 0.03 0.4
Bagasse (sugar cane) ae 0.09 0.9
Rumen fibers (manure) 0.2 0.3 126
Paper
Corrugated fibreboard = O98 jal
Computer print out = 0.9 1.4
Key punch holes = 0.8 ae
Milk carton (polyethylene coat) a 130 dt
Newspaper a 0.6 1.0
Municipal trash fractions
Black Clawson 0.7 On 2
Bureau Mines = 0.6 0.9
Relative to ball milled newspaper (56% sacch.) = 1.0. Substrates whose relative value is
1.0 or better are considered good substrates for hydrolysis.
tion of reaction time at three enzyme activity levels are shown in Figs. 6, 7,
and 8. Figure 9 shows the weight of glucose produced and percent saccharifica-
tion realized as a function of enzyme activity level for a fixed reaction time of
twenty-four hours. Final glucose concentrations ranged between 1.6 to 4.6
percent and increased with either enzyme activity or substrate concentration.
Final saccharification ranged from 33 to 77 percent and increased with enzyme
activity, but decreased as the substrate concentration increased.
Milling, rather than chemical pretreatment, is preferred by the authors for
increasing the reactivity of the raw materials. The costs of milling and chemi-
cal pretreatment are approximately the same. The encouraging results ob-
tained with hydropulped substrates may prove to be most significant in cutting
substrate pretreatment costs, thereby improving the overall economics of the
process.
Having proved that this process is technically feasible, the Natick Develop-
ment Center is conducting an intensive pre-pilot plant study to optimize all
variables and to obtain the engineering and economic data needed for the
design of a demonstration plant. The pre-pilot plant was engineered in collab-
289
TABLE 7
Industrial wastes for conversion
Saccharified at 50°C, pH 4.8 with T. viride QM 9414; cellulase 0.08—1.5 w/ml (ave. 1.0).
Substrate Relative % saccharification 24 hours?
5%
dry wt. As rec’d As rec’d Ball
wet dry milled
Percent saccharification > 1 as received
22 Nicolet sulfite pulp if. 2 0.8 ib 7/
15 Hydropulped Govt. documents 1.3 123 5
16 Hydropulped Govt. documents cael 0.9 1605)
21 Nicolet kraft pulp = 0.8 1.5
12 Kimberly Clark tissue mill waste 1.0 1.0 steal
! 1 St. Regis paper mill sludge 1.0 0.9 0.9
| 2 St. Regis glassine (PVD) waste = 0.8 0.9
3 St. Regis glassine (wax) waste — 0.8 0.6
Percent saccharification > 1 if ball milled
13 Cotton linters (miles) aa 0.2 ee)
18 Corey paper mill waste 0.5 0.3 2,
14 Extracted oat hulls (Hoffman La Roche) = 0.1 te
20 Nicolet waste filler 0.6 0.5 iLaal
23 Rye grass straw (Miles) = 0.3 elk
17 Covey paper mill waste 0.6 0.5 120
26 Hercules wood chips = 0.1 1.0
25 Welches seedless grape pomace = 0.6 0.9
19 Stuley corn fiber = 0.3 0.8
24 Welches grape pomace = 0.5 0.7
“Relative to ball milled newspaper (ave. 42% sacch.) = 1.0.
TABLE 8
Hydrolysis of hydropulped Government documents in 1 liter Str, 50°C, pH 4.8
Sample Enz. conc. S conc. Hydrolysis at 24 hrs
No. (u/ml) % dry wt.
Glucose Saccharification
(mg/ml) (%)
15 0.5 2.3 16 64
, 16 0.5 4.8 23 43
16 0.5 wa ies | 26 30
1) 16 1.0 2.3 20 77
16 1.0 5.0 33 59
16 1.0 7.5 39 47
16 5 2.4 21 79
16 1.5 5.2 39 67
16 1.5 eS 46 53
Enz. = cellulase of T. viride QM 9414; S = pulped documents as rec’d, wet;
glucose mg/ml xX 0.9 100
% Saccharification = ae
5 mg/ml (original)
290
z
se O
E <
fe?) U
E ve
ws <
O r
Og U
= <
S) ry,
SS
0 5 10 15 20 25
TIME (hrs.)
80
2.5% S
60
°
40 5.0% S$
7.5%S
20
0
0 5 10 15 20 25
TIME (hrs.)
Fig. 6. Hydrolysis of hydropulped Gov’t documents by Trichoderma viride cellulase.
[E] = 0.5 units/ml (FP).
40 7.5%S
5.0% S
Ee. 30
SS
0)
E
w 20 2.5% §
VW)
O
O
=
10
©)
0
0 5 10 15 20 25
TIME (hrs.)
SACCHARIFICATION
Yo
80 2.5% §
60 5.0% S
7.5%S§
40
20
0
0 5 10 15 20 25
TIME (hrs.)
Fig. 7. Hydrolysis of hydropulped Gov’t documents by Trichoderma viride cellulase.
[£] = 1.0 units/ml (FP).
i)
Me)
Je
50
7.5% S
Of 5.0% § 5 80 2.5%S
2 x 5.0% S
2 30 = 60
ow 7.5%S
oT
O 25%S
oO 20 ; U 40
> O
= <
O Y,)
10 5° 20
0 0
0 5 10 15 20 25 0 5 10 15 20 25
TIME (hrs.) TIME (hrs.)
Fig. 8. Hydrolysis of hydropulped Gov’t documents by Trichoderma viride cellulase.
[E] = 1.5 units/ml (FP).
50 | 7.5%S 100
Ww
- = 80 0
= O 2.5 ‘° S
N =
ne <I 50%5
ce 60
a 7.5% §
D <
E Za
© 40
bhi we)
a <
O os
S 20
= os
rb)
; 0
0 0.5 1.0 1.5 0 0.5 1.0 1.5
ENZYME CONC. units/ml (FP) ENZYME CONC. units/ml! (FP)
Fig. 9 Relationship of T. viride cellulase activity level to 24 hour glucose yield and percent
. Saccharification in the hydrolysis of hydropulped Gov’t documents.
292
oration with Fermentation Design, Inc. of Bethlehem, Pa., and comprises the
following equipment:
(1) Fermenters
(2) Enzyme reactors
(8) Holding tanks and auxiliary vessels
(4) Instrumentation modules
(5) Substrate handling and preparation equipment
(6) Enzyme recovery and concentration equipment
The design and construction is such that the most sophisticated fermentation
techniques including batch, continuous, and semi-continuous processes can
be studied (Fig. 10).
ENZYME CELLULOSE
RECOVERY NUTRIENTS
AIR
WASTE CELLULOSE
ENZYME
STORAGE
T. VIRIDE
FERMENTATION
ENZYME I.
ENZYME tank “SOLID
REACTOR RECOVERY WASTE
GLUCOSE SYRUP
GLUCOSE © SCP ETHANOL CHEMICAL
RECOVERY FEED STOCKS
Fig. 10. Enzymatic conversion of waste cellulose.
Because of the sophistication of the monitoring and control instrumenta-
tion, both fermentation and enzyme hydrolyses are continuously monitored
and controlled to optimize the output of the individual processes.
The initial capacity of this equipment is 1000 lbs. of cellulose per month.
With minor modifications the capacity may be increased possibly four-fold.
This equipment is now operational at the Natick Development Center.
The potential world-wide impact of this process on the food, energy and
ecology problems has been recognized both nationally and internationally.
Upon completion of these studies, it will be possible to engineer larger pilot
demonstration plants and possibly full scale plants with confidence. Many
national and international chemical companies, pulp and paper mills, processors
of agriculture products and various governments have shown definitive interest
in the exploitation of this process. Because of this interest, the U.S. Army
Natick Development Center is working very closely with several industrial
firms to assure the transfer of this new technology to commercial scale as soon
as practicable for the benefit of the nation and mankind.
CONCLUSIONS
(1) The enzymatic hydrolysis of cellulose is technically feasible and practi-
cally achievable on a large scale by 1980. The glucose produced can be con-
verted to food products, fuel and chemical feedstocks.
(2) The exploitation of our fossil fuel reserves — coal, oil shale, etc. — may
satisfy our energy demands for the next five to ten decades. However, the
ultimate long-range solution to the world’s energy problem may well be the
development of practical and economical processes to harness the inexhaustible
energy of the sun.
REFERENCES
1 Reese, E.T., Mandels, M. and Weiss, A.N., 1972. Cellulose as a novel energy source. In:
T.K. Ghose, A. Fiechter and N. Blackbrough (Editors), Advances in Bioengineering.
Springer Verlag, Berlin, 2nd edn., p. 181—200.
2 Mandels, M. and Kostick, J., 1973. Enzymatic hydrolysis of cellulose to soluble sugars.
U.S. Patent 3,764,475. —
3 Goldstein, I.S., 1974. The potential for converting wood into plastics and polymers or
into chemicals for the production of these materials. NSF-RANN Report, Dept. Wood
_ and Paper Science, School of Forest Resources, North Carolina State at Raleigh, N.C.
4 Mandels, M., Hontz, L. and Nystrom, J., 1974. Enzymatic hydrolysis of waste cellulose.
Biotech. Eng., 16: 1471.
Reese, E.T., personal communications.
Mandels, M., 1975. Microbial sources of cellulase. Biotech. Eng., in press.
Brandt, D., Hontz, L. and Mandels, M., 1973. Engineering Aspects of the Enzymatic
Conversion of Waste Cellulose to Glucose. AIChE Symposium Series 69, No. 133,
py i 27133.
AD oO
SUPPLEMENTAL BIBLIOGRAPHY
1 Ghose, T.K., 1969. Continuous enzymatic saccharification of cellulose with culture
filtrates of Trichoderma viride QM6a. Biotech. Bioeng., XI: 239.
2 Ghose, T.K., 1972. Enzymatic saccharification of cellulose. U.S. Patent 3,642,580.
3 Ghose, T.K. and Kostick, J., 1969. Enzymatic saccharification of cellulose in semi
and continuously agitated systems. Ad. Chem. Ser., 95: 415.
4 Ghose, T.K. and Kostick, J., 1970. A model for continuous enzymatic saccharification
of cellulose with simultaneous removal of glucose syrup. Biotech. Bioeng., XII: 921.
5 Hottel, H.C. and Howard, J.B., 1971. New Energy Technology. MIT Press, Cambridge,
Mass., p. 4.
6 Katz, M. and Reese, E.T., 1968. Production of glucose by enzymatic hydrolysis of
cellulose. Applied Microbiol., 16: 419.
294
7 Mandels, M., Hontz, L. and Brandt, D., 1972. Disposal of cellulosic waste materials by
enzymatic hydrolysis. Army Science Conference Proceedings, Vol. 3, AD 750. 351:
L6—o4.
8 Mandels, M., Kostick, J. and Parizek, R., 1971. The use of adsorbed cellulase in the
continuous conversion of cellulose to glucose. J. Polymer Sci., Part C., 36: 445.
9 Mandels, M. and Weber, J., 1969. The production of cellulases. Adv. Chem. Ser.,
95: 391.
10 Mandels, M., Weber, J. and Parizek, R., 1971. Enhanced cellulase production by a
mutant of Trichoderma viride. Applied Microbiol., 21: 152.
11 Andren, R.K., Mandels, M. and Medeiros, J., 1975. Production of sugars from waste
cellulose by enzymatic hydrolysis. In preparation.
Ce)
Resource Recovery and Conservation, 1 (1976) 295—313
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
ENERGY FROM REFUSE BY BIOCONVERSION, FERMENTATION AND
RESIDUE DISPOSAL PROCESSES*:**
JOHN T. PFEFFER and JON C. LIEBMAN
Department of Civil Engineering, University of Illinois, Urbana, Ill. 61801 (U.S.A.)
(Received 19th March 1975)
ABSTRACT
Biological conversion of organic refuse to methane by anaerobic fermentation is one
mechanism by. which the energy in urban waste can be reclaimed. Laboratory studies have
been used to determine the rate and quantity of gas production at various operating tem-
peratures. The dewatering characteristics of the spent fermentation slurry have been
evaluated. The spent solids can be dewatered to a sufficiently low moisture content such
that incineration is selfsustaining. The incineration system has been evaluated to determine
the possible energy recovery from the spent cake. A process for treating the liquid blow-
down from the system has been developed.
A mathematical simulation of the total system has been constructed to evaluate per-
formance under various Operating conditions. The operating cost of the system can be ob-
tained. A plant processing 908 metric tons of refuse per day will produce 3905 m? of
methane per hour. If the methane is marketed for $3.53/100 m’, the system will require
a dump fee for refuse disposal in excess of $5.34/metric ton. Sale of recovered steam from
the incineration of the spent cake can reduce the dump fee by about $3.00. Recovery of
just methane provides an efficiency of energy recovery of 32.6 percent. This efficiency can
be increased to 63.4 percent if the steam from the incinerator can be sold.
INTRODUCTION
Among the many challenges confronting the world as a whole, and the
United States in particular, are two seemingly unrelated problems. The first
and perhaps the more obvious of the two is the problem of solid waste dispos-
al. The second is the decline in certain energy resources as evidenced by the
increasing shortage in natural gas reserves. The development of a process to
convert organic refuse to methane would provide at least a partial solution to
both of these problems.
Anaerobic digestion has been used for decades in wastewater treatment to
*This research was supported by the National Science Foundation, Research Applied to
National Needs under Grant No GI-39191
**Paper presented at the Symposium ‘‘Energy Recovery from Solid Waste”, March 13--14,
O75:
296
effectively reduce the quantity of organic sludges and to transform them
into stable, more easily dewatered residues. The reduction is accomplished by
the biological conversion of the organic solids to methane and carbon dioxide.
Since anaerobic processes have a very low efficiency of biological energy con-
version, most of the energy of the substrate is lost. The gas produced has a
high energy content and is a valuable end product with potential for reclama-
tion.
Various studies have demonstrated that organic refuse, in particular garbage,
is amenable to anaerobic decomposition. Organic refuse is composed basically
of the same compounds (carbohydrates, proteins and fats) as sewage sludge,
though in different relative proportions. There appears to be no reason why
refuse cannot undergo adequate anaerobic decomposition. Proper environ-
mental conditions must be maintained, the deficient nutrients supplied and
potential toxicity problems controlled.
Using existing technologies developed for producing refuse derived fuel
(RDF), it is possible to produce a light fraction that can be used as substrate
for the anaerobic fermentation process. Laboratory studies were conducted to
evaluate the quantity and rate of gas production, reactor slurry dewatering
characteristics, and residue disposal. Data obtained from these studies, plus
those available in the literature, were used to construct a mathematical simu-
lator of the entire process. This simulator was used to evaluate the performance
of the system under various operating conditions.
QUANTITY AND RATE OF GAS PRODUCTION
To determine if a biological process could be developed that would effec-
tively convert municipal refuse to methane, a series of laboratory studies was
undertaken to establish the kinetic relationships at various operating tempera-
tures. This work is discussed in detail elsewhere [1—3]. The pertinent results
are shown in Fig.1 and Table 1. Figure 1 shows the gas production (dry gas
TABLE 1
Volatile solids destruction (percent )*
Temperature Retention time (days)
(°C)
4 6 8 10 15 20 30
35 16.5 26.4 28.6 29.8 32.0 32.7 34.0
40 31.0 33.6 35.7 36.8 39.0 39.9 40.7
45 26.7 29.0 31.2 32.3 34.1 35.4 36.4
50 34.9 38.6 41.0 42.2 44,2 45.4 46.1
55 40.4 42.6 44.5 45.2 47.2 48.2 49.1
60 “ar 46.6 48.3 49.6 50.8 51.8 52.4
“Percentage of organic material in the raw refuse that is converted to gas.
i)
ie)
~]
0.45
0.30
0.25
TOTAL GAS PRODUCTION _m?/ kg V.S. ADDED
0.20
0 5 10 15 20 25 30
REACTOR RETENTION TIME - DAYS
Fig. 1. Gas production obtained from the digestion of municipal refuse (dry gas at 0°C and
atmospheric pressure).
at O°C and atmospheric pressure) obtained at various temperatures and reten-
tion times. The substrate used in these studies was shredded refuse obtained
from the USEPA Center Hill Laboratory in Cincinnati, Ohio. The volatile
solids destruction in Table 1 was calculated from the gas production. Because
of the characteristics of the substrate and the laboratory reactors employed,
it was not possible to obtain the solids balance necessary to measure volatile
298
solids destruction accurately. It is important to note that the maximum
volatile solids destruction was only 52.4 percent. A significant portion of the
material added to the fermenter remains for final disposal.
The original laboratory studies used completely mixed digesters having an
operating volume of 15 liters. Additional data were collected from a 400-liter
digester that was operated at a 10-day retention time and at 60°C. When
refuse obtained from a local landfill was used as substrate for the larger unit,
gas production was 0.39 m°/kg (6.3 scf/lb) volatile solids added as compared
to gas production of 0.40 m°/kg (6.55 scf/Ib) for the 15 liter units operating
at 60°C and a 10-day retention time (see Fig.1). However, when the large
digester received refuse obtained from the Madison, Wisconsin shredding
facility, the gas production was only 0.32 m?/kg (5.22 scf/lb) of volatile
solids added. The gas yield was 18 percent lower than that previously obtained
from the large reactor. When refuse obtained from the St. Louis-Union Electric
project was used, the gas production was only 0.31 m*/kg (5.0 scf/lb) of
volatile solids added. This low gas production apparently resulted from aerobic
composting that occurred while the wet refuse was being transported and dried
for storage. While gas production may vary with feed stock, the variation will
not be excessive.
The effect of temperature on gas production is pronounced. The optimum
mesophilic temperature was found to be about 40°C. At 43°C, inhibition of
gas production was significant. Gas production at 45°C was only slightly
greater than at 835°C. The maximum gas yield in the mesophilic temperature
range was 0.29 m?/kg (4.65 scf/lb) of volatile solids added. The gas yield was
substantially greater in the thermophilic temperature range, with the maximum
being 0.45 m?/kg (7.25 scf/lb) of volatile solids added.
The rate of gas production is much greater in the thermophilic temperature
range. At 60°C the gas yield from a system operating at a 4-day liquid retention |
time was about 85 percent of that obtained at a 30-day retention time. The |
gas production at the 4-day retention time (60°C) was greater than that ob-
tained from digesters operating at 40°C temperature and 30-day retention
time.
SLURRY DEWATERING—VACUUM FILTRATION
The characteristics of the digester slurry, in particular the dewaterability,
were investigated. Laboratory evaluation of the vacuum filtration system was
conducted using the filter test leaf technique. The results of these studies are
shown in Fig.2. A coarse weave filter cloth was employed. No chemicals were
used to condition the slurry before dewatering. Solids capture was not high,
but since a major portion of this filtrate is expected to be recycled, high solids |
capture was not considered to be important. !
Exceptionally high filter cake yields can be obtained from vacuum filters if |
the solids concentration in the feed slurry is high and a dry cake is not required’
However, if it is necessary to produce cake with a low moisture content, the |
!
299
5.0 CAKE SOLIDS
4.0
<
=
aot
E
o +-3.0
S
t)
a
im
= 2.0
[a4
ey)
=
—
i
1.0
1 2 3 4 5 6 7 8 9
FEED SOLIDS CONCENTRATION PERCENT
Fig. 2. The effect of feed solids concentration and cake solids on filter yield, no chemical
conditioning.
loading on the filter is greatly reduced. The addition of a polymer (Nalco
73C32) significantly improved the dewatering characteristics. These results
are shown in Fig. 3. With unconditioned slurry at 3 percent feed solids, filter
yields of 48.8 and 97.6 kg/m?-hr (10 and 20 lbs/ft?-hr) resulted in a cake with
a solids content of 24 and 20 percent, respectively. With conditioned slurry
at the same feed concentration, a filter yield of 48.8 kg/m?-hr was achieved
with a cake containing 30 percent solids, and a filter yield of 97.6 kg/m?-hr
was achieved with a cake containing 27.5 percent solids, both substantial in-
creases over the unconditioned slurries.
The polymer dosages used in the first series of test runs were based on the
fine suspended solids in the feed and these dosages were chosen on the basis
of specific resistance values determined in preliminary work [4]. The dosages
used were not necessarily optimum. To determine the approximate optimum
dosage, a series of tests was run with 3.3 percent feed solids using a 30-second
form time and 3-minute dry time, and varying the polymer dosage from 0 to
5.4 percent. The results of these tests are given in Table 2. From these data it
would seem that the optimum dosage at 3-percent feed solids was about
2 percent. There was no substantial improvement in filtrate suspended solids
or cake solids as higher dosages were used.
While the results clearly show the advantages of using polymers to improve
vacuum filtration results, the costs associated with polymer use must be con-
300
CAKE SOLIDS -
FILTER YIELD - 100 kg/m--hr
3 4 Se, 6 7 8 9 10
FEED SOLIDS CONCENTRATION - PERCENT
Fig. 3. The effect of feed solids concentration and cake solids on filter yield when slurry
was conditioned with polymer (Nalco 73C32).
TABLE 2
Optimization of polymer dose for 3.3% feed solids?
Polymer Form rate Filter yield Cake Filtrate solids (g/l)
dose (kg/m?-hr) (kg/m?-hr) solids
(% of FSS) (%) TS SS DS
0.00 WPA ee 27.8 10.05 6.42 3.63
1.09 163 23.3 29.3 6.05) 0 270 Sea |
DAT 169 24.2 31.1 3.79 0.55 3.24
3.26 185 26.4 31.6 3.385 ~ 0.14 PE |
4.35 166 23.8 33.0 3.76 0.65 See
5.43 161 23.0 33.6 3.24 0.23 3.01
“FSS = feed suspended solids, TS = total solids, SS = suspended solids, DS = dissolved solids.
sidered. Since vacuum filtration is only one step in the total system, the
impact of this process on the remaining processes must be considered. High
filter cake solids will reduce the cost of auxiliary fuel for residue incineration,
or the haul and landfill costs if the residue goes directly to a landfill. Also,
an increase in filter yield will reduce vacuum filter costs. The cost of the
polymer must be offset by the cost reductions.
|
The following conditions were assumed in evaluating the cost of polymer
conditioning of the slurry prior to vacuum filtration. With a feed slurry of
6 percent, a filter yield of 56.1 kg/m?-hr (11.5 lbs/ft?-hr) at 25 percent cake
solids would be expected with unconditioned slurry. Conditioning the slurry
with polymer (1.25 percent of feed suspended solids) would increase the cake
solids to 30 percent at a filter yield of 56.1 kg/m?-hr. With polymer priced at
$0.66/kg ($0.30 per lb), the polymer cost alone would be $2.30 per metric
ton of refuse received or $87.30 per hour for a 908 metric-tons-per day sys-
tem. The savings possible in the downstream process do not warrant such cost.
This will be discussed later in more detail.
SLURRY DEWATERING — CENTRIFUGATION
Dewatering tests were conducted using a solid bowl conveyor (model P-600
Super-D-Canter) centrifuge unit obtained on loan from the Sharples Division,
Pennwalt Corporation. This unit was tested using the slurry from the 400 liter
reactor. The slurry was pumped from a mixed storage tank to the centrifuge
at a constant rate with a Moyno positive displacement pump. The centrifuge
was operated for one to two minutes at each test condition prior to sampling
the cake and the centrate. The machine was operated at 5700 rpm, producing
a centrifugal force of approximately 3200 X g. The results are shown in
Table 3 and Fig. 4.
' Based on these data, a full scale machine of similar characteristics could
process a maximum flow of 0.85 m?/min (226 gpm), or a maximum solids
loading ranging from 1476 kg/hr (3251 lbs/hr) per machine for a cake solids
of 38.3 percent to 2099 kg/hr (4624 lbs/hr) per machine for a cake solids of
27 percent. -As can be seen from Fig.4, the conveyor speed relative to the
centrifuge bowl speed was the major factor in determining the cake solids.
An increase in the flow rate had little or no effect on the cake solids ata
conveyor speed of 10 rpm. However, the solids loading does play a major role
as the solids-flow rate approaches the machine capacity. From these observa-
tions, it appears that the solids-handling capacity of the machine limits the
concentration of solids in the cake, particularly when the reactor slurry con-
tained 5 percent or more solids.
Solids capture was not high in these tests, ranging from a low of 63 percent
to a high of 90 percent. This high carry-over was a result of the presence of a
substantial concentration of fine solids present in the slurry as well as poor
capture of the fibers under certain test conditions. Chemical conditioning
would improve this capture, but at a cost. Since this liquid is expected to be
recycled back into the fermentor, solids capture is of limited significance.
RESIDUE INCINERATION
The ability to produce a cake with solids concentrations of 30 percent or
greater with the centrifuge system has substantially improved the economics
302
TABLE 3
Sharples P-600 centrifuge results
Flow Conveyor speed Cake solids Centrate solids (g/1) Suspended solids
(lpm) (rpm) (%) capture (%)
Total Suspended
Pond setting 3%, feed total solids 28.3 g/l
4.9 10 38.5 aj 7 a
22 34.9 — = +
36 32.8 ori a a
53 30.6 = = <a
10.0 10 39.4 = 2 i
22 39.9 8.26 5.06 80.6
36 33.8 9.45 5.94 77.6
53 30.3 8216-26 80.0
Feed total solids 28.6 g/l
18.5 10 37.6 EOS 17203 72.7
16 32.7 11.10 6.93 73.3
27.6 10 38.3 ihietor St al 7 Tig
16 29.1 LAAOL EDS 72.3
Feed total solids 21.4 g/l
958 16 32.5 9.50 5.20 70.4
13.2 16 30.3 9.86 5.51 68.7
16.7 16 31.2 11.22 6.44 63.5 :
20.1 16 33.6 ft-20 “6.50 62.8 |
Feed total solids 43.8 g/l
20.1 10 No separation, solids overload
16 34.2 12.44 7.40 82.6
28 27.0 10.01 4.54 89.9
Pond setting 3, feed total solids 25.7 g/l
13.6 10 36.3 9.78 spats? 16:8
16 36.2 10:19.5 5.95 73.8
32 34.4 9.27 5.66 75.2
53 32.7 9.20" D399 74.0
associated with the incineration of the dewatered residue. There are two
major gains associated with incineration. First, disposal by landfill of the large
quantities of organic residue represents a substantial cost in urban areas. The
costs of hauling to acceptable landfill sites would greatly influence the econ-
omics of this system. Secondly, the installation of a waste heat boiler in the
incineration system would provide more than enough steam to satisfy the |
process heating requirements and would improve the energy recovery efficiency,
even if the excess steam energy could not marketed.
40
py ee te
x<
30 path ik req uastzeae
LiJ
co
uJ
Qa
J
2 FLOW FEED SOLIDS
= 20 o 4.8 gpm 2.83%
m x 10.0 &pm 2.83%
¥ O 18.4 2pm 2.86%
om © 27.6 &pm 2.86%
10 ® 20.0 2pm 4.38%
0
0 10 20 30 40 50 60
CONVEYOR SPEED - RPM
Fig. 4. Cake solids produced by a Sharpless P-600 centrifuge under various operating
conditions.
A total energy balance was made for the incineration system. The basis
for this balance was the energy input from the organic residue. Initial bomb
calorimeter data showed a calorific value for the residue of 17 X 10° J/kg
(7334 BTU per lb) of dry solids or 22.7 X 10° J/kg (9734 BTU per lb) of
volatile solids. These data were for refuse from Madison, Wisconsin. Calorific
values for the air classified light fraction from St. Louis are listed in Table 4.
TABLE 4
Calorific values for St. Louis refuse and residue
Volatile J J
solids eee ea tee reren ru AS acd a 2
(%) __ kg total solids kg volatile solids
Air classifier
light fraction 66.4 14 x 10° 21.6 xX 10°
Digester residue Ta 18.5 x 10° 24 x 10°
304
140
50% EXCESS AIR 120
100
25% EXCESS AIR
t.
=
™s
x
wo
oO
. =
= '
™
=) >
~ 80 &
Ss aS
a re
1 ce
QO -
= =
Si a
= =
~—
— r <4
Li uJ
iz =
a.
40
20
25% EXCESS
AIR 50% EXCESS
AIR ' 0
24 | 28 32 36 40
CAKE SOLIDS - PERCENT
Fig. 5. Auxiliary fuel requirements and heat recovery potential for incineration of the
digester residue.
The digester residue has the higher energy value in terms of both total dry
solids and volatile solids. This is expected since cellulose is the primary
material being fermented. Lignin, which is relatively non-biodegradable, has
a higher energy value than cellulose. Therefore, the higher lignin content in
the residue will cause an increase in the heating value.
An equal, if not more important, factor in this increased energy value is
the higher proportion of plastics in the residue than in the raw refuse, since
plastics do not degrade in the fermentation process. With as much as one-half
of the organic material being converted to gas, the plastic content in the
residue would be nearly twice the raw refuse content. Plastics have a very
high calorific value.
Based on a carbon, hydrogen and oxygen + Gale the chemical composition
of the residue was estimated from measured compositions of raw refuse. This
composition was used to calculate the theoretical air requirements at 9.76 kg
of air per kg of volatile solids. By performing a heat balance on the incinerator,
Fig.5 was constructed. This figure shows the auxiliary fuel requirements and
potential heat recovery for incineration of cake with various moisture con-
tents. With 50 percent excess air and a furnace temperature of 760°C (1400°F),
the cake solids must be about 35 percent for combustion to be self-sustaining.
Reducing the excess air to 25 percent reduces the required cake solids to
about 30 percent. Cake solids below these values will require auxiliary fuel.
Heat recovery from the incineration of the residue is desirable. The process
heat required for maintaining the digestion temperature and for mono-ethanol
amine (MEA) regeneration from the carbon dioxide scrubber is significant.
The potential heat recovery in cooling the stack gas from 760°C to 315°C
(1400°F to 600°F) is shown in the upper curves in Fig.5. At a cake solids
content of 30 percent and 25 percent excess air, approximately 90 X 10? J/hr
(85 X 10° BTU/hr) can be recovered from a 908 metric ton (1000 ton) per
day plant with the digestion system operating at 60°C and a 10-day retention
time.
Additional heat can be recovered if the stack gases are cooled to a lower
temperature. The installation of an appropriate preheater or economizer could
recover an additional 26 to 32 X 10° J/hr (25 to 30 X 10° BTU/hr) by cooling
these gases to 150°C (300°F). The availability of a market for this steam will
determine how efficient the recovery system should be.
TREATMENT OF FILTRATE—CENTRATE
The liquid generated from the residue dewatering process is of very poor
quality: dissolved solids range from 4 to 5 g/l, increasing with increasing re-
cycle of this liquid to the fermentation system; suspended solids range from
4 to 6 g/l or higher, depending upon the dewatering process (see Table 5).
A number of processes have been screened as candidate systems for treating
this liquid. The only process that appears to have potential for reducing the
pollution potential of this stream is chemical coagulation. The results of
preliminary jar tests showed that iron salts can coagulate the fine solids and
produce a supernatant that is low in suspended solids.
A series of tests was conducted to evaluate the use of ferric sulfate with
and without organic polymers (Nalco 73C32) as coagulants for this liquid.
When ferric sulfate only was used as a coagulant for the liquid prior to
306
a
initiating centrate recycle, the data listed in Table 6 were obtained. A
standard jar test procedure was employed in these tests. The pH was adjusted
to the values shown in the table prior to coagulant addition. At reduced pH
levels, lower iron dosages were required to achieve a substantial reduction in
COD and suspended solids. Since ferric ion reacts with hydroxide, the higher
iron requirements at the higher pH levels were probably required to reduce
the pH to an optimum level.
TABLE 5
Filtrate-centrate characteristics
Recycle ratio
0 0.5
Total solids 8350 mg/l 10507 mg/l
Suspended solids 4600 mg/1 5930 mg/l :
Volatile solids 4340 mg/1 6093 mg/l
COD 7057 mg/l mg
TABLE 6
Filtrate coagulation with ferric sulfate
Filtrate pH Fe,(SO,), X H,O Supernatant (g/1)
tot. solids dose
(g/l) (g/l) Tot. solids Dis. solids Sus. solids COD
10.795 6.0 1.5 5.482 5.015 0.467 2.347)
1.6 5.059 5.058 0.001 1.1089
dey, 5.058 5.008 0.050 1.22
O275 6.5 a 5.713 4.840 0.873 3.40 ©
222 4.800 4.732 0.068 1.346)
2.3 5.640 5.547 0.093 1.750
9.329 7.0 2.6 5.058 4.654 0.404 2.45
7 | 4.848 4.850 0.008 1.153)
2.8 5.180 4.740 0.440 2.394
Additional studies were conducted on the centrate from the 400 liter
reactor operating with a 50 percent recycle. These data (see Table 7) show
that the pH had a very pronounced effect on the clarification efficiency of
the coagulant. The pH shown in this table is the adjusted pH after coagulant
addition. A final pH of 4.2 provided very good suspended solids removal even
with ferric sulfate dosages as low as 0.9 g/l. At the higher chemical dosage,
the supernatant was very clear at the lower pH. However, high dosages of iron
and polymer did not achieve a clear supernatant at a pH of 6.2.
307
TABLE 7
Effect of pH and chemical dose on clarification
Fe,(SO,), X H,O Polymer __ Final Suspended solids (mg/1)
(g/1) (mg/1) pH
Centrate Centrate Supernatant
and chem.
1:5 100 6.2 4930 6693 102
iS) 100 4.5 5581 6087 3 Oe
ales) 50 4.5 5581 5844 16
dhe 100 6.2 4930 6240 135
0.9 100 4.5 6776 7620 50
0.9 50 4.5 6776 7640 50
These data also show that the polymer dosage was of little significance in
the efficiency of solids removal. The results were not affected at either the
50 or 100 mg/l dosage. The polymer was more important in determining the
character of the sludge produced. Not only clarification efficiency, but also
the settling velocity and final volume of the resulting sludge are important.
The settling characteristics of the resulting sludges were evaluated using
small laboratory settling columns. These columns were one-liter graduated
cylinders fitted with a stirrer mechanism operating at a speed of approximately
2 rpm. These data are shown in Table 8 for various coagulant dosages and at
a pH of 6.2 and 4.5. C, is the initial concentration of suspended solids in the
coagulated centrate; and C,, is the suspended solids concentration obtained
in the sludge after 3 hours of settling. Iron dosages of 1.5 g/l and polymer
dosages of 100 mg/l] gave the highest settling velocity (V;) and highest sludge
solids concentration. The pH was highly significant with this coagulant dose.
A pH of 4.5 produced a reasonable settling velocity and sludge concentration.
Because of the small settling columns, caution must be exercised in extra-
polating these data to large-scale systems. One can expect the sludge to settle
but at a rather low velocity. Consideration should be given to an alternate
TABLE 8
Settling characteristics of centrate sludges
Iron Polymer pH Cy V. Cu
s
(g/l) = (mg/l) (g/l) (cm/sec) (g/1)
1.5 100 6.2 6.24 2.8x107° 12.0
12 100 6.2 6.69 2.800 * 12.0
0.9 50 4.5 TCR es AES atO. 9.8
0.9 100 4.5 7-62 0) De x0"? tt .O
1.5 50 4.5 BrO9n ETO" Or* seul
1.5 100 4.5 5.84 Oe! a Gol Oa 15.8
308
dewatering system such as a centrifuge. The large volume occupied by the
settled sludge will require treatment of approximately twice the volume of
water needed for blowdown. This will substantially increase both capital and
operating costs for treatment of this water. Based on observations of the
ability of a solid bowl basket centrifuge to concentrate these solids, it is
probable that a solids concentration of 10 percent could be obtained. This
concentration would greatly reduce the volume of water to be treated for
blowdown purposes. Data have not been obtained to substantiate this observa-
tion, but the prospect appears promising.
The use of a centrifuge also has significance in dewatering the resulting
sludge. The specific resistance of the settled sludge was measured to determine
its dewatering characteristics. The specific resistance, r, was found to be
5.66 X 10° sec*/g for the highest coagulant dose at a pH of 4.5. For the lowest
coagulant dose, r was 1.65 X 10!° sec?/g. These are both. very high specific
resistance values. Low filter yields would be obtained if a vacuum filter were
used for dewatering of this sludge. The low volume of water — 0.378 m?/min
(100 gpm) — expected to be processed suggests that it would be more practi-
cal to take the flocculated slurry directly to a solid bowl centrifuge for both
clarification and dewatering of the cludge.
COMPUTER ECONOMIC STUDY
In order to explore the economic implications of the process, a computer
simulation was constructed. This program permitted investigation of the ef-
fects of changes in operating parameters and system designs on the overall
process. The process flow sheet shown in Fig.6 is one of the systems that was
simulated.
The program consists of individual subroutines for each unit process from
receipt of raw refuse to disposal of the dewatered residue. Each subroutine
receives information from the preceding routines on the quantity and quality
of the material entering the simulated process. Empirical design and cost
relationships are used to determine design parameters for the process and to
calculate mass, energy, and cost balances. The subroutines are designed to be
independent of one another so that alternate unit process steps may be inter-
changed. For example, subroutines for dewatering by centrifugation and
vacuum filtration are interchangeable in the program.
The capital cost routine for the simulator is not complete. It includes only
the installed costs for the various processes. Such items as land, site prepara-
tion, engineering, legal, fiscal, interest during construction etc. have not been
included. The data presented are for the purpose of comparing alternate
schemes for the process and do not represent total costs. Therefore, these
data must be used accordingly.
Table 9 shows selected results from runs of the entire process with in-
cineration of the cake and landfilling of the ash and heavy fraction. This
system was sized for 908 metric tons (1000 tons) per day of refuse. Run 1
Tromme]
Unload
Sirota
Storage shred Inert
Fines
Gas
Light
5 a
Raw Sev'age
Sludge 1
Fermentor
(60°C)
a
Tank
Liquid Recycle
Fig. 6. Schematic of proposed system.
TABLE 9
Results of simulation
Run number iL
Digester temp. (°C) 60
Detention time (days) 6
Digester feed conc. (%) 10
Digester volume (1000 m*) 30.3
Centrifuges req’d (No.) 9
Digester costs ($/hr) Fig eS)
Centrifuge costs ($/hr) 48.50
Incinerator cost ($/hr) 63.35
Methane (m?*/hr) 3905
Construction costs ($1,000,000) 14.29
Capital costs ($/hr) 185.50
x costs ($/hr) - 405.67
215.33
Net income ($/hr)
Magnetic
Separation
Ferrous
(Salvage)
; CH,
E 560
A f “
309
Air Separate
| '
Heavy Light
Inert Organics
(to energy
recovery)
Combustion
Products
Dewater
ae
Ash
Blowdown Incinerator
(Treat)
2 3 4 5
60 60 50 40
8 6 8 8
10 15 10 10
40.4 20.0 20.1 40.4
9 9 10 11
80.90 64.70 81.41 ro er a (
48.50 48.50 53.95 59.39
61.92 63.64 67.99 12.28
4045 3877 3424 3000
14.90 3.56 i> ou 16.18
190.87 179.02 199.73 207.03
412.60 398.75 425.26 2 ies 5)
213.40 2IV25 178.74 153.65
310
serves as a base run; the other runs demonstrate the effect on the process of
variations in design parameters. Run 2 shows the relative insensitivity of the
process to digester retention time. The higher construction cost for the di-
gester is offset by a lower incinerator construction cost and a higher gas in-
come. Capital is assumed to be available at 6 percent; a higher interest would
slightly increase the cost of the system in Run 2. Using these cost relation-
ships, the cost of gas at higher retention times needed to have a net income
equivalent to the 6-day retention time would be $3.58 and $3.67 per 100 m?
($1.014 and $1.04 per 1000 scf) at 8-day and 10-day retention times, respec-
tively.
Run 3 shows a substantial savings due to a much lower construction cost
for the digester when a higher feed-solids concentration is employed. Runs
4 and 5 show added costs associated with the lower temperature of digestion
due to an increase in the cost of residue dewatering and incineration. Also,
the gas income is lower.
The system shown in Figure 6 can be priced for 908 metric tons per day
(1000 ton/day). The construction costs are shown in Table 10. These cost
TABLE 10
Construction costs
Shredder? 1,375,000
Separation? 592,000
Storage? 950,000
Fermentation? 2,230,000
Centrifuge ° 2,050,000
Incineration? 5,060,000
Gas purification? 2,032,000
Total 14,289,000
7Cost data from Wise et al. (1974) [5].
°Cost data from Patterson and Banker (1971) [6].
“Cost data from manufacturer [7 ].
data have been adjusted to July 1973. This analysis shows that approximately
65 percent of the construction cost is associated with the fermentation and
residue disposal processes. The centrifuge system and incineration accounts
for 50 percent of the construction costs.
The economic justification for this added investment is shown in Table 11.
Residue disposal by sanitary landfill after vacuum filtration has a low capital
requirement. However, with a haul and disposal cost of $3.30/metric ton
($3.00/ton) of wet cake, an operating cost of $153.72/hr is added to this
system, giving a total dewatering and disposal cost of $192.18/hr. Substitu-
tion of the centrifuge for vacuum filtration adds a higher capital and operating
|
|
311
TABLE 11
Residue disposal versus costs
Temp. 60°C, feed solids 10%, 90% volatile, time 6 days
Construction Total cost ($/hr)
Vacuum filter 1,315,000 23.01
Cake (25% solids) p< 153.72
Inorganics a 15.45
Total 1,315,000 1G zgilys
Centrifuge 2,048,000 48.50
Cake (35% solids) ae 109.67
Inorganics ad 15.45
Total 2,048,000 173.62
Centrifuge 2,048,000 48.50
Incineration 5,058,000 63.35
Credit for process heat = —36.01
Ash ae 3.00
Inorganics ra 15.45
Total 7,106,000 94.29
costs for dewatering. The cost savings in residue disposal due to a drier cake
compensates for this higher dewatering cost. The total residue dewatering
and disposal cost is only $173.62/hr. This system will probably still cost less
than the vacuum filtration system when the total capital requirements are
considered.
Incineration of centrifuge cake with landfill of the ash yields a total cost
for residue dewatering and disposal of only $94.29/hr. In addition to a very
substantial cost reduction in haul and landfill costs, recovery of heat for
heating of the digesters and regeneration of MEA gives a credit of $36.01/hr.
Even with a greatly increased capital cost, this system has a much lower cost
than either of the two previously discussed systems. Of course, haul and
disposal costs greater than $3.30/metric ton will only increase the cost reduc-
tion due to incineration.
A detailed analysis of the costs for the base run is shown in Table 12. The
shredding and separation processes have a relatively low construction cost.
The shredder has a high power and maintenance cost. The cost of shredding,
separation and storage, exclusive of operating labor, is $92.26/hr or $2.43/
metric ton ($2.21/ton) of refuse processed. The fermentation process has a
significant construction cost plus a high cost for heating and chemicals. The
chemical cost results from the large quantities of nutrients required. With
nitrogen priced at $330/metric ton, this cost becomes significant. If adequate
sewage sludge were available, the nitrogen in this sludge could be used to
reduce the nutrient cost.
35 LA :
TABLE 12
Cost analysis (37.9 metric tons/hr)
Const. cost Operating cost ($/hr) Maint. cost Total
($/hr) Fig A ee a ER OS ae a eh ($/hr) ($/hr)
Chem. Power Heat
Shredder Dede a 14.26 = 22.13 58.11
Separation 9.31 7 3.27 3.43 16.01 9§
Storage 14.94 == 2eL0) = 1.16 18.14 ©
Fermentation ZO AT 45.96 3.19 21.38 2.58 93.28 ©
Centrifuge 32.20 = 4.45 = 1V8S 48.50 ©
Incineration 55.16 — ~ — 8.20 63.36 —
Gas processing 32.00 0.30 1.55 14.63 2.35 50.83
Total 185.50 46.26 28.82 36.01 51.64 348.23
Construction cost is the major cost in the remaining processes. The centri-
fuge system does have a significant maintenance cost and a significant quan-
tity of heat is required for the regeneration of the MEA. There are additional
minor costs associated with the above processes that have not been identified.
Table 12 includes only the major cost items.
The efficiency of energy recovery is dependent upon the type of system
employed. An energy balance is presented in Table 13. The recovery efficiency
in a system solely producing methane is only 32.6 percent. Because of the
large amount of organic material remaining, a significant increase in efficiency
can be obtained by incinerating the organic residues. If a market for this
TABLE 13
System energy balance (10° J/hr)
Energy available 378.3
Refuse 358.3
Sludge 20.0
Energy consumed 70.0
Power (2780 HP, 30% Eff.) 25.0
Heat (85% Eff.) 45.0
Total energy input 448.3
Energy produced 284.1
Methane 146.3
Heat (incineration) 137.8
Recovery efficiency
Methane only 32.6%
Actual eT Pe fe
Potential 63.4%
313
steam could be obtained, 63.4 percent of the energy input possibly could be
recovered. There is a use for part of the recovered steam in the process. By
using incinerator heat for the process requirements, 42.7 percent of the input
energy can be recovered in the form of methane.
REFERENCES
1 Pfeffer, J.T., 1968. Increased loadings on digesters with recycle of digested solids.
Journal of Water Pollution Control Federation, 40: 1920.
2 Pfeffer, J.T., 1973. Processing organic solids by anaerobic fermentation. Proc. Inter-
national Biomass Energy Conf., The Biomass Energy Institute, Winnipeg, Canada,
p56.
3 Pfeffer, J.T., 1974. Reclamation of energy from organic refuse. EPA 670/2-74-016,
National Environmental Research Center, Office of Research and Development, U.S.
Environmental Protection Agency, Cincinnati, Ohio.
4 Pfeffer, J.T. and Liebman, J.C., 1974. Biological conversion of organic refuse to
methane. Annual Report NSF/RANN Grant No. GI-39191, Dept. Civil Engineering,
University of Illinois, Urbana, Ill., Report UIUL-ENG-74- 2019.
5 Wise, D.L., Sadek, S.E. and iene R.G., 1974. Fuel gas production from solid wastes.
Deena Bee No. 1207, Dynatech R/D Co., Cambridge, Mass.
6 Patterson, W.L. and Banker, RBs, VO. Bermetine costs and manpower requirements
for conventional wastewater treatment facilities. Water Poll. Control Res. Series
17090DAN 10/71, U.S. Environmental Protection Agency, Washington, D.C.
7 Personal communication, 1974. Sharples Division, Pennwalt Corp., Oak Brook, Ill.
“Sg eae to aes] Fe } dimometinpyieasoog ant ar ee 10:
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Resource Recovery and Conservation, 1 (1976) 315
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
Short communication
GOODYEAR TIRE-FIRED BOILER*
E.R. MOATS
The Goodyear Tire & Rubber Co., Akron, Ohio 44316 (U.S.A.)
(Received 19th March 1975)
Recognizing the potential energy source of the 165-million tires discarded
annually in the United States, The Goodyear Tire & Rubber Company is
testing a method of heat generating from whole tire combustion in a tire-
fired boiler at its Jackson, Michigan, tire plant.
This furnace, originally designed by Lucas American Recyclers, was chosen
after an investigation of tire-fired boiler equipment suppliers by Goodyear’s
Corporate Engineering Department in 1971. The basic furnace design was
developed by Lucas Furnace Development, Ltd., of England with the engi-
neering design and construction being rendered by Lucas American Recyclers
and Fluor Utah. The design included a furnace with the design capability of
burning 32.7 metric tons (36 tons) of scrap tires per day and a boiler to
generate 11,338 kg (25,000 pounds) of steam at 1.7 X 10° Pa (250 psi) per
hour. Stack gas cleaning equipment was incorporated as a contingency to
reduce particulate and SO, emissions (though tires contain less than one
percent sulfur) to comply with possible air pollution standards.
The furnace operates continually without supplementary fuel at a tem-
perature high enough (1093°C at the center) to melt all the non-combustible
material such as bead wire and fiber glass. It utilizes a rotary hearth which is
sloped to a central ash discharge port. This hearth is refractory lined and
water cooled around the center to protect its metallic body from the high
temperatures developed inside the furnace.
Gases rise in a vortex that causes smoke and odor molecules to be con-
sumed. An inert ash is all that remains after the whole tires complete the
burning cycle. |
Tires are fed onto the hearth from a vestibule by means of a pusher ram.
Tires enter the vestibule through a door which closes as the furnace door
opens to receive the tires. The hearth can revolve at rates of from 1/4 to 8-1/2
revolutions per hour with its rate set manually so that the tires are completely
consumed in two revolutions. (In normal burning, hearth rates are in the
range of 2.7 to 6.0 revolutions per hour.)
The tire-fired boiler thus meets the needs of the American society today;
it generates cheap steam at no drain on fossil fuel sources while contributing
a viable solution to the disposition of a troublesome solid waste component.
*Paper presented at the Symposium ‘‘Energy Recovery from Solid Waste”, March 13—14,
1975.
Resource, Recovery and Conservation, 1 (1976) 316—318
© Elsevier Scientific Publishing Company, Amsterdam — Printed in The Netherlands
Book review
Resource Recovery and Utilization. Edited by H. Alter and E. Horowitz,
American Society for Testing and Materials, 1975, 200 pages, price $20.
This book is the proceedings of the National Materials Conservation Sym-
posium and Workshop on Resource Recovery and Utilization held in April/
May 1974 at the National Bureau of Standards in Gaithersburg, Md., U.S.A.
The objective of the meeting was to bring together the technology and im-
plementation of conservation, which is reflected in the content and layout
of the book. This is a particularly helpful approach with the current state of
the art and political attitudes.
The book is divided into five parts of approximately equal length, of which
the first introduces the subject and sets the scene with U.S. trade data and
reactions of a major industry to the problems and possibilities of conserva-
tion. This is followed by two interesting papers on what might be called the
business aspects. These include discussions on the problems of placing con-
tracts for recovery systems with local government and providing the neces-
sary financing.
The third part reviews the technology currently available for solid waste
recovery. Included here are descriptions of demonstration systems in current
operation or planned; a more detailed examination of one system; and a dis-
cussion of the range of unit operations available for recovering non-ferrous
metals. Five significant materials are singled out for more in-depth study in
the fourth part which considers ferrous metals, aluminium to represent non-
ferrous metals, glass, plastics and paper. All are examined from the positive
approach of practical recovery and provide useful up to date information.
These are followed by reports from workshops on each of these five mate-
rials recovery areas. While maximum benefit was no doubt obtained from
those attending the sessions, the reports are very valuable in that they pro-
vide a topical and practical assessment of the situation for each materials
followed by specific recommendations for encouraging and implementing
recovery schemes.
The book provides an interesting and valuable picture of current techno-
logy, practice, and attitudes to conservation in the United States, although
most of the content is equally valid in any industrialised area of the world.
It is therefore recommended as a concise statement of current thinking on
solid waste recovery.
A.V. Bridgwater
University of Aston in Birmingham
enti
Book review
The Energy Conservation Papers. Edited by Robert H. Williams, Ballinger,
Cambridge, 1975, 377 pages, price $ 17.50 cloth bound, $ 8.95 paperback.
The Energy Policy Project — a study which concluded that the ‘‘best’’
national energy policy was that which would encourage energy conservation
used this collection of commissioned research papers, in part, as source
material. The consequent occasional duplication and overlap, nonunitormity
of terms and other minor evidences of independently working contributors
is more than compensated by the sustained quality of presentation of widely
ranging but related information — and setting it into a framework for useful
application.
Two of the six contributed chapters directly address energy substitution/
recovery from wastes; a third deals with energy impacts/requirements of
specific pollution (waste) control strategies; and a fourth chapter on econom-
ic impacts is closely supportive. Two remaining contributed chapters discuss
transportation options and impacts. These chapters are supported by 15 ap-
pendices, extensive chapter notes, and thoroughly referenced sources. A
somewhat disjunctive but nevertheless valuable bibliography is included. An
unfortunately inadequate index (and a table of contents occasionally omit-
\ting titles) leaves the reader rather on his own. But it is clear that this com-
pact collection will — or ought to — soon become an often reached for and
well thumbed reference, particularly suited to two purposes: to provide
systems planning (but not actual design) information; and as an heuristic tool
for creative insight and idea production leading to waste and transportation
management solutions which satisfy the complex technological and econom-
ic ramifications which underly conventionally-approached solutions, There
are more than enough updates and new tabulations to motive the reader-user
to throw away his carefully garnered files and folders — at least of aggregate-
level data.
The chapter on metals recycling is illustrative of the general format. In
this instance, three metals: iron, aluminum, and copper, are depicted as com-
modity flow systems; with their relationships among sectors and markets
quantified. Energy demands, primary and recycled, are developed: carried
back to major system components, e.g., coal mining for iron production;
waste shredding. A realistic total conservation potential of about 0.4 quads
can result by utilizing these metals in U.S. urban waste. The chapter on
organic wastes (it includes feedlot and crop residues) which concentrates
(but not exclusively) on methane production concludes with a current net
energy potential of about 3.6 quads for the U.S. The chapters on transporta-
tion policy and consumer options/impacts are equally extensive, thorough,
and wonderfully illuminating.
318
These papers may be regarded as a concise source book — not complete,
to be sure — but invaluable for comprehensive systems analysis and design
of waste-to-energy management programs and transportation systems.
Jerome F. Collins
JOURNAL OF THE WASHINGTON ACADEMY OF SCIENCES
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VOLUME 66
Number 2
Jour nal of the JUNE, 1976
WASHINGTON
ACADEMY ..SCIENCES
‘Issued Quarterly
a), Washington, D.C.
CONTENTS
Features
H. GUYFORD STEVER: Science, Engineering and Social Change ........
J. PHIL CAMPBELL: The Role of Research in Agriculture............... 131
CAROL J. LEHTOLA: Experiences of an Engineer, Who Happens To
BS BV OITIEIN Sol diale ee ee cle & hicks tte elke Sia nie cloner ciorated aslo cece cee et otic oe
Profile
RAYMOND J. SEEGER: Benjamin Franklin, American Physicist .........
: Research Reports
KINGSOLVER, J. M.: The Correct Identity of Stator bixae (Drapiez)
With Lectotype Designation (Coleoptera: Bruchidae) ................. 147
KINGSOLVER, J. M.: A New Species of Amblycerus from Panama
(Coleoptera: Brachidae) ih ..< 5.5 aise. Sooke wien wae w ece eine ee ag eee ele as
Academy Affairs
The Awards Program of the Academy and Recent Honorees ..............
ING WRLC HO SUSE sett tat iam rier ie Ss ant nd Soe ateeni eacteat wince rb eyeing ea, ae 156
SclemistscmutheNOWS) «sh on ks dcrkeieic sou eS ses ode b ne walle dw Pane dein eles 158
Obituaries
Norman H. C. Griffiths .... »<oarias\pipemmec 162
Marjorie Hooker ....... MOON i oekaki ha |, aR oe nae 162
: A F
Washington Academp of Sciences
EXECUTIVE COMMITTEE
President
Florence H. Forziati
President-Elect
Richard H. Foote
Secretary
Alfred Weissler
Treasurer
Richard: H. Foote
Members at Large
Norman H. C. Griffiths
Patricia Sarvella
BOARD OF MANAGERS
All delegates of affiliated
Societies (see facing page)
EDITOR
Richard H. Foote
EDITORIAL ASSISTANT
Elizabeth Ostaggi
ACADEMY OFFICE
9650 Rockville Pike (Bethesda)
Washington, D.C. 20014
Telephone (301) 530-1402
Founded in 1898
The Journal
This journal, the official organ of the Washington Aca-
demy of Sciences, publishes historical articles, critical
reviews, and scholarly scientific articles; proceedings
of meetings of the Academy and its Board of Mana-
gers; and other items of interest to Academy members.
The Journal appears four times a year (March, June,
September, and December) — the September issue
contains a directory of the Academy membership.
Subscription Rates
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Single Copy Price....... 4.00
Single-copy price for Vol. 66, No. 1 (March, 1976)
is $15.00.
Back Issues
Obtainable from the Academy office (address at bot-
tom of opposite column): Proceedings: Vols. 1-13
(1898-1910) Index: To Vols. 1-13 of the Proceedings
and Vols. 1-40 of the Journal Journal: Back issues,
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Published quarterly in March, June, September, and December of each year by the
Washington Academy of Sciences, 9650 Rockville Pike, Washington, D.C. Second class
postage paid at Washington, D.C. and additional mailing offices.
DELEGATES TO THE WASHINGTON ACADEMY OF SCIENCES,
REPRESENTING THE LOCAL AFFILIATED SOCIETIES
Binlaseaphical Society of WaSniMOton. .. 65 = 26.6 v2 ois 6 Sees cos ve ne eld oe chee es Ralph P. Hudson
Panurepolorical Society OF Washington ... 5.22.2. 00s fede cee oe ee ee cee ee ecg ees Jean K. Boek
EMPTIES OCIClV Ole WV ASHMMPLON s.55-2)) el iy ors bl ees ee ee tee ce ead Slee whales wh ds Inactive
ae TE SOCICHY OF NV ASMINGTON: seiere 6 os was cid ols Ose ee are Sine ww a sed aes ak b eh vod ee eell David Venezky
Pemeiarical’ Socicty Of Washington 3. 2. os5065 okks eee eee wees aoe be abe ane eu oes Maynard Ramsay
MER GCE AIC SOCIGLY 6.64. Giese ba cross Saye es dre be ole oo eS v ea slsa Se aes 4 Alexander Wetmore
PEILD ISS SOG CORA ENS NTT) 00) gen ee Charles Milton
Memeaesecic yor the District of Columbia... ce. 0 sete s fe be Rhos ewe be ds teehee ee Inactive
Sea aT AM AOS 90K CAN SOC ICE Var fsa. ays eh coe sais ca neds Sgn a Da ae Un ole A DIRE a bua weeds Paul H. Oehser
Pee eMMESRCICI VEO WASHINGTON) 65). 6s. 5s cic oo a cee Rl OS 8's Hab RO ASHE eee EOS Conrad B. Link
SE TLEEY Cif ANTRSVETORT IT BCT Pot 5 ee saa ea ee Alfred A. Wiener
Seat RE SOCICHY, Ol PNGIMCEIS:.¢ | .e c.2 ce con oa schwis ehe eee cles eacs cess Seeetes George Abraham
insarurcon Electrical and Blectronics Engineers... .. 4.5.2. 2s nee ee eee George Abraham
PmbHeanesectcty of Mechanical ENgineers .... 60s) os sad eee ee cde cde sae eee de Michael Chi
Hemmunhological Society of Washington 2... 2.0560 2000.0. sie ce cece ee eee eee James H. Turner
Pee HE SOCICLY. 10f MICTODIOIORY 5 sei ots «oc code ne ees sis Bee ws eas a else Sadree ess Thomas Cook
Parmer merican Military ENSINCEDs ..6 o..ce se cos ok wed cs cece cess ee eesacaucees H.P. Demuth
American Society of Civil Engineers .............. Peete SPIE arate ens ade Ores ovei cise: ts Shou Shan Fan
ReMicuvaieiee xpenmental Biology and MeGICINE . . 2.6.2.5 6.06. ccs ceeds eee e eee ena wde Donald Flick
A SRE ESTP SDGTS RY LEOTe I ISTE SR GS oe Glen W. Wensch
MaectinatienaleAssociation Of Dental Research... ..... 0)... osc ce ee cee ew eee e eae nes No delegate
American Institute of Aeronautics and Astronautics ............. 0. ccc cece cece eens Franklin Ross
Pe ERE (COLOlOPICal SOCICLY ~.. «Susi so ceceicice cs Wok vise b's Sie owls c ea ee oa ele 6 wbaes A. James Wagner
MP eMIMCESEEICUVL OF VVASHINETON < 5.5. < snes Oc kon ie ce Unio beide wc oe ewig le elde ses Robert J. Argauer
AE DLS ST SDCTE ECT IMA U1 11S (C2 ne gr Gerald J. Franz
Ee TMI Ae SOCICLY go ee ok EE ee oe eS IE Le UE she Bde eee Dick Duffey
ame EOIOOM, TECHNOIOGISES, 220.5 5 sicca oS ned oats we ewe doe Salado blenlew waa Fs William Sulzbacher
A CUEFIOED CSAUCITC SIUC Te 0s lense re ein Ue, aS a RPC Po Ap ie ene A Inactive
eee PMC TRANS CU SOCIOL Yoo test Cara sna toaesod oe AEN oe SiS La EO eS Hae Delegate not appointed
DC Pane TISE OLY “Ol. SCIENCE GIUD 35 fog. ic. 0 scare sv uw so 8 Ree RES Ok bce 6 Mek ads Inactive
Pmencanesssociation Of Physics Teachers ii. 0.0 0s... 2256 2s NSN ee bs eh ea ee Bernard B. Watson
ees ENP IN AOL AGHCLICD 5: 5..o ssi Ne Sin Fok oh hina bw traces Neraleteleiaeta aie Ronald W. Weynant
PEMchicanE Society. of Plant PhySiOlOgistS: «6. acs Soc ice os ek news eee owen wees caw Walter Shropshire
Piauaeren) Operations: Research Counell .. 2.5.6.5 5. 56a ce se ede ont ode T a wee de ss John G. Honig
a AES OCC TY “Ole ATTIOHI CAN coo oir Nie uses nha cue tts sae ene MV SIS Ls RR OG wa as Clee Inactive
American Institute of Mining, Metallurgical
aE UEC TIE PARE CUS ee. oye, eee sy he ic ce oars ces ee Aten ie Lae 2s Carl H. Cotterill
Cen Ee AIM Ol ANS TF OMGOTMENS 156 i Sate se Cees sees GAY aS OE Saks aa SO eee John A. Eisele
Bee BCA ASSOCIILION, OL PAMICIICA® 2 h.00c.c 0k ahs's 0295 oie akg vk oo Oke os eae se Patrick Hayes
eS AIOE CLICHHSES Cte re oe cs Bein ik Caan ds sha woe & eRe Ln Miloslav Recheigl, Jr.
BEES CUOIOCICAl ASSOCTALIOIN 2 2.0 wi ils'c se. ciel eke beidrece'e. odode moeke Bok. bine OLA w wee BRR John O’ Hare
Delegates continue in office until new selections are made by the representative societies.
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976 125
— 126
Ie
FEATURES
Science, Engineering, and Social Change!
H. Guyford Stever
Director, National Science Foundation and Science Advisor to the President,
Washington, D. C. 20550
The role of the after-dinner speaker
seems to be growing more difficult each
year. Today’s speaker is expected to
address the serious issues of our time
and come up with answers. At the same
time, he is expected to be entertaining,
and to keep in mind such things as the
high cost of babysitting, and the desire
of some of his audience to get home on
time to catch the 11 o’clock TV news.
The worst fate is to be speaking on a
Monday evening, knowing that all the
men in your audience are silently cursing
you for each play and instant replay of
Monday night football they miss.
Fortunately, this is not Monday night.
Nevertheless, Ill try to take the other
factors into consideration. I want to
speak broadly, and briefly, on a subject
that I think is of importance to us not
only as members of the engineering
community but also as citizens —citizens
of arather problem-filled, perplexed, and
impatient world.
There are a number of reasons why it
is such a world. Two of them are science
and engineering, and their offspring,
technology. I am not blaming science or
technology for our current predicament.
Others have made this a pastime and a
profession by attempting to prove that
science and technology have somewhat
‘ Presented at the Annual Banquet, Washington
Society of Engineers, Nov. 21, 1975, National
Aviation Club, Washington, D. C.
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
obtained a life of their own and taken
us in directions we did not want to go.
I do not believe this. Science and tech-
nology have given us, at each point in
history, what we wanted or thought we
wanted. They have been among our prin-
cipal forces for social and environmental
change, and will continue to be. It is only
today — within recent years—that we are
beginning to realize the extent to which
this process, with both its good and bad
effects, has been taking place, and the
consequences it holds for the future. In
short, we have gained an important new
insight into the relationship of science
and technology to social and environ-
mental change. And this insight, as evi-
denced by the great surge of public in-
terest and participation in the direction
and management of technological change,
indicates what may be the beginning of
a new maturity and wisdom on the part
of society in dealing with its future.
That technology has been a major initi-
ator of social change can be seen every-
where in the past. This is true, for ex-
ample, in the role it has played in changing
the condition of women in society. Take
the matter of Women’s Lib. With all due
respect to the present influence of the
Betty Friedans, Gloria Steinems, and
Germaine Greers in influencing the activi-
ties and outlooks of women today, there
were others over the years whose work
changed women’s lives, and sometimes
quite radically. Unfortunately, they were
127
all men, with such names as Elias Howe,
Alexander Graham Bell, C. L. Sholes,
Gail Borden, Clarence Birdseye, and
Charles Kettering. It was their innova-
tions which changed the conditions and
positions of women in society as much
if not more than the social champions of
their era. Take for example, the invention
of Elias Howe—the sewing machine.
Before this invention, four-fifths of all
clothing in America was made in the
home. The sewing machine moved most
of that activity out of the home and into
the factory, and with it, both for better
and worse, came changes in the lives of
millions of women.
Bell’s invention of the telephone and
Sholes invention of the typewriter had
similar effects. They literally helped
create the working girl, and the condi-
tions that led to women’s suffrage. At
the same time the innovations of men like
Borden in canning and later Birdseye in
frozen foods changed the work of women
in the home. And I mentioned Charles
Kettering of General Motors because it
has been said that his invention of the
automatic starter put women in the
driver’s seat in more ways than one, and
perhaps liberated women more at the
time than the work of Susan B. Anthony
and her suffragettes.
Just so I may give equal time to the men
in this audience, let me mention that there
were a number of inventions that changed
the lives of men too. Many of these were
what we might consider today simple
innovations, yet they changed the course
of history and the face of continents. One
was the invention of the stirrup, which
placed the knight on horseback and
allowed the growth of the feudal system.
Another was the invention of barbed
wire, which opened the western United
States to ranching and farming.
These may seem like small, inconse-
quential changes alongside those taking
place today. Yet they are the kind of tech-
nological influences that continue to grow
and have implications, both predictable
and unknown, for the future. For example,
no one would have considered a few
years ago that today’s refrigerants and
128
aerosol propellants might pose a future
threat to the environment and human
health. But there is mounting evidence
that this may be the case.
At the same time the continuing revolu-
tion in food processing raises some inter-
esting questions related to our eating
habits and our future nutrition. One
reason for this is because two-thirds of
today’s meals are now eaten away from
the home, and the percentage is growing.
The result is that the control of our nutri-
tion is going more into the hands of the
food processing and food service indus-
tries, with many scientific and regulatory
implications. (I learned this, by the way,
at an NSF seminar recently conducted
entirely by women nutrition experts.)
As I mentioned before, it is very
significant that we have now begun to
question and seek better control over the
relationship between our scientific and
technological changes and their effects
on society. And I would like to spend
the balance of my remarks on a few
aspects of this situation—what it means
for science and engineering, the Govern-
ment, and the public.
This new awareness of the large-scale
social and environmental effects of
science and technology adds a substantial
number of new responsibilities and diffi-
culties to those already borne by the
science and engineering communities.
For those of us on the optimistic side
we prefer to call them challenges and
opportunities. Nevertheless, they will
make great demands on us in terms of
calling for more and better basic research,
greater ingenuity and innovation in
applying what we learn so that it can
serve the best interest of society, and
efforts to establish a closer working
relationship with that society. This last
demand must include a strong move to
improve public understanding of science
and technology. It must particularly
convey a better knowledge of their limita-
tions as well as their potentials, and an
understanding of the costs, risks, and
benefits involved in the technological and
social alternatives being offered to
society by science and engineering. This
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
is an especially important matter in the
kind of participatory and activist society
evolving today. Unless we can improve
the lines of communication and the
dialogue between the expert and the
citizen, we are going to be a society that
is neither technologically sound nor polit-
ically satisfied—one in which we will
not have the best technologies available;
one of public confusion, distrust, and lack
of support.
In all cases involving scientific and
technological knowledge and innovations
the public has a right to know—and
should know—what these are, how they
work, and how they can affect its future.
There are a great many ways that this is
being done today, particularly through
public hearings involving environmental
matters such as the siting of powerplants
and other public engineering projects
which come under Federal regulation and
are subject to NEPA—the National
Environmental Policy Act. Most of you
are quite familiar with this so I won’t
go into detail on it. The National Science
Foundation, however, is now expanding
on this concept of involving the public
in scientific and technological affairs
through new programs we are consid-
ering in our Science Education Direc-
torate. One of these—called Science and
the Citizen—will seek to bring the
experts and the average citizen closer
together. It will support a program that
will allow scientists and engineers on
university faculties, and their graduate
and undergraduate students, to meet with
citizens’ groups to discuss and advise
them on matters of public decisions
involving complex scientific and tech-
nical knowledge. Beginning the first of
next month, we are going to hold a series
of regional meetings in seven major cities
to get the public’s reaction and input to
this proposed program.
On a broader scale we are supporting
Science education programs in our
schools and universities that should lead
to improved science literacy on the part
of all our future citizens. We hope this
will facilitate the process of making wise
choices when it comes to choosing among
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
complex technological options in the
years ahead.
Up to this point I have been empha-
sizing the roles of the experts and the
public in the discussion of technological
assessment and alternatives. Let me say
a few words about the Government’s role.
That role is critical for a number of
reasons. One of these is that the Federal
Government supports about 60% of the
Nation’s research and development, and
particularly the R & D which determines
long-term trends in technology. This, of
course, does not preempt private in-
dustry from research that will lead to
important breakthroughs, but it does
make it more likely that industry will
get much of its impetus for innovation
through Federally supported work. We
are, therefore, concentrating a great deal
of effort these days on making the
research results that come out of this
work available to industry and to State
and local government. This effort goes
under the name of ‘resource utili-
zation’’—the resource being chiefly
knowledge—which is going to have an
increasing influence on how well we use
all our material and energy resources
in the years ahead.
Another way that the Federal Govern-
ment influences the flow of the best
research and technologies into public
use is through its regulatory powers, and
through the incentives and disincentives
it can create through legislation, taxes,
subsidies, and so forth. We are very
interested in and concerned about this
matter today, and trying to come up with
more and better ways to get new and
advanced ideas into public use so that
they can be accepted and take hold
economically. This includes such con-
cepts as the solar heating of buildings.
As I’m sure you know, Federal
agencies and the Congress are strongly
involved in the matter of technology
assessment—examining the possible
long-range environmental and _ social
effects of proposed technologies and new
technological and social systems. The
Congress has its new Office of Tech-
nology Assessment, and we at NSF have
129
an Office of Exploratory Research and
Systems Analysis (ERSA), responsible
for supporting research in this field.
Technology assessment is a relatively
new field and is considered by many at
this point to be as much an art as ascience.
With this in mind, and interested in
finding out what people in Government,
the universities, industry, and various
professions thought about the matter,
NSF a few years ago sponsored an
extensive survey, part of which was
devoted to finding out what subjects these
people thought would be important candi-
dates for an assessment. More than 600
experts were polled and they came up
with some 188 technologies. The list
holds a great variety of concepts, some
quite possible to implement today or in
a few years, others requiring probably
years of work before they could be
adopted. And they deal with social as
well as technological concepts. Here are
a few examples from that list:
e Fabricated foods using soy and other
protein bases properly textured and
flavored.
e Bacterial and viral substitutes for
chemical pesticides.
e Electrical power generation using
nuclear breeder reactors.
e Government data bank recording
social security, tax, medical, mili-
tary service, criminal, educational,
and other information on nearly
everyone.
e Automated hog farming.
Sperm and ova banks.
e A national population dispersion
policy leading to the creation of new
towns.
e Chromosome typing for abnormali-
ties in humans within weeks of
conception.
e Accredited TV colleges and univer-
sities.
e High speed trains (200 miles per
hour) connecting large cities.
e Limited weather control.
e Alimony insurance.
Those are a small number—a rather
random sampling—of the 188 tech-
130
nologies suggested for assessment. I
chose those particular examples because
they include some ideas that are essen-
tially here and in use today, others
possible soon and already being debated,
and a few that are still only remote
possibilities. For example, we already
see in our supermarkets a few food items
fabricated from protein bases that have
been accepted by the consumer. But this
is On a very small scale. If this were to
be developed extensively, and we as a
nation began to switch largely to soybean
and alfalfa-based foods in place of meats
for our protein, the changes in our agri-
cultural economy as well as those of
other nations could be very significant.
Such changes would have their effect
on our land and water management, our
energy use, employment, and many other
situations. And we don’t know how
strong these effects would be.
In the case of the adoption of the
breeder reactor, there is already a
national assessment taking place on
several levels—within the Government
and by public interest groups—with the
outcome perhaps several years off.
We have seen a few small examples
of population dispersion to new towns
such as Reston and Columbia. But what
would happen if a national decision was
made to do this on a very large scale
throughout the country?
We know the dangers of using chemical
pesticides, but also their advantages.
What would a shift to bacterial and viral
pesticides mean? How would it affect
agricultural productivity? What would its
long-range implications be for wildlife
and human health?
And as far as tampering with human
conception, genes or even matters related
to marriage and divorce, these also have
complex and far-reaching consequences,
many of which are already being debated.
I have intentionally mixed technical
and social innovations in my list because
I think we are going to find them increas-
ingly overlapping in their activities and
influences. Hence, we are going to find
assessment a field growing in its inter-
disciplinary aspects and in the need for
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
people of widely different interests and
disciplines to cooperate closely. This
means that, perhaps, physicists and
psychologists, seismologists and social
scientists, and even engineers and ento-
mologists may find themselves working
together in ways they never imagined.
Of course, there will be a great number
of us in science and engineering who will
not be involved in this way, but will
remain concerned primarily with ad-
vancing our own fields, broadening the
base of knowledge, refining existing
technologies, and innovating in familiar
areas. In this way we will be laying the
groundwork for our incremental progress
and the development of alternatives to
those new ideas which go through the
mill of assessment and are found wanting.
Now that we are so acutely aware of
the possible environmental and social
implications of our new technologies we
will need more than ever enough alter-
natives and new ideas to be flexible and
avoid the crises that come from de-
pending too heavily on any one break-
through or purported panacea. I think
we are slowly beginning to see that we
live in a world where the only permanent
thing is change, and where even con-
ditions of stability are dynamic. This does
not mean we cannot pursue a utopian
vision or hold on to and live by long-
cherished values. It does mean we have
to grow in our knowledge and under-
standing, and in our science and tech-
nology, to control and direct the changes
they can bring. If we do this it is possible
to build a society and a world that, if not
perfect, is at least free from many of the
problems and fears we face today. And
that, I believe, is a very worthwhile— and
obtainable — goal.
The Role of Research in Agriculture’
J. Phil Campbell
Under Secretary of Agriculture, Washington, D. C. (retired).
Of all the modern miracles fashioned
and achieved by man—from television
to atomic energy and space exploration—
none has proved more beneficial to
mankind than American agriculture. Yet,
fortunately for the world, the dimensions
of its future have not yet been discovered.
Granted, we have been blessed with
hundreds of millions of acres of fertile
land in the United States and a climate
ideally suited to continuing bountiful
' Presented at a joint meeting of the Washington
Academy of Sciences and the Helminthological
Society of Washington, November 20, 1975,
Cosmos Club, Washington, D.C.
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
agricultural production. Still, there are
other countries which have not yet begun
to match our agricultural production,
even though they, too, possess quantities
of arable land.
There are good reasons American
agriculture leads the. world.
First, we inherited and nurture a
politico-economic system that encourages
farmers to produce. No other political
system has ever provided so well for a
nation as the continuing American
Experiment. At the same time, no other
economic system can coax so much
efficient productivity from the farmer and
his coworkers in the food chain as
131
America’s capitalistic free enterprise
system.
Secondly, our American agricultural
miracle springs from a unique system of
scientific discovery and information dis-
semination that invariably meets and
usually surpasses the needs of its time.
It is a system that is supported by the
American people through all levels of
their government, as well as through
private enterprise, the scientific com-
munity, the educational system and the
farmer themselves.
Our winning combination is incom-
parable. Yet we want to share the pro-
duction that flows from our labor and
genius as well as the know-how that
produced our success. Practical as well
as generous, Americans know they can-
not feed all the world today, much less
the world of tomorrow, and that the more
nations which benefit from adoption of
our successful methods, the better.
Millions in the underdeveloped world
need the kind of productivity that science
and the farmer have achieved in America.
Consider:
e The time required to produce 100
bushels of corn in America has
dropped from 135 hours to just 6
hours in 60 years.
e The number of man-hours required
to produce 100 bushels of wheat
dropped from 106 to 9 in the same
period.
e In 1970-74, it took somewhat less
than 1 American man-hour to pro-
duce 100 lbs. of turkey. In 1910-14,
it took nearly 4 working days (31.4
man-hours).
e One hour’s farm labor now produces
nearly 9 times more than it did in
192%.
e In 50 years, U. S. crop productivity
per acre has more than doubled.
e The average farm worker in the
United States today supplies food
and fiber for 52 persons. Just 10 years
ago he was producing enough for
29. By comparison, a farm worker in
the Soviet Union today produces
enough for only 8 persons, while
132
a farm worker in France produces
enough for only 14.
e While an estimated one-third of the
work force in the Soviet Union is
engaged in agriculture, only 5% of
the work force in America is em-
ployed on farms. The other 95% is
free to produce such consumer
goods as refrigerators and auto-
mobiles, and to provide such needed
services as medical care.
e There were 242 times as many
farmers in America in 1950 as there
are today, yet agricultural output in
this country last year was twice what
it was 20 years ago. Obviously, we
must be doing something right.
Frankly, it is time the world recognizes
and applauds those scientists—past and
present—who have painstakingly per-
severed throughout the years to provide
our farmers with the keys that unlocked
such productivity.
Consider, for instance, the men and
women through the years who made it
possible for the United States to produce
half of the world’s corn in today’s market.
The development of hybrid corn and its
utilization in the United States has
become a classic example of the team-
work between scientist and farmer which
made the American agricultural miracle
possible. In the 1930s, 22 bushels per
acre was the average corn yield in the
United States. Today, the average is
about 95 bushels per acre. In 1973, one
farmer actually produced 306 bushels per
acre. And we’re still working with corn,
changing its color, its growing habits and
its nutritional content. ~
The number of our successes is
virtually endless, and the range is equally
impressive. Not only do we breed leaner
hogs to meet changing consumer pref-
erences, but we feed them better and
keep them healthier. Scientists and
farmers and those who help them have
practically eliminated hog cholera and
cattle brucellosis, two deadly livestock
killers, in this country.
It is the genius of man which stands out
when we look closely at the miracle of
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
American agriculture. The golden soy-
bean, said to be the world’s most effec-
tive producer of protein per acre, has a
history in the Orient that goes back more
than 3,000 years, yet it achieved its
present great stature as a hunger fighter
in the United States. Even the chicken
is not anative American bird, but a jungle
fowl of India and the Far East, brought
to this country by the first European
settlers. Which nation coverted the
Sunday special dinner into an everyday
feast at the dinner tables of millions of
people? You guessed it. America.
The economic benefits of such scientific
progress are immeasurable. Marek’s dis-
ease in poultry, for instance, was costing
the United States more than $200 million a
year until an effective vaccine was devel-
oped. Now losses have been cut by more
than 70%. Sometimes our successes
sound like the alchemy of changing lead
into gold. Scientists in my native state of
Georgia, for example, converted one of
nature’s peskiest grasses, common ber-
mudagrass, into an outstanding forage
plant by cross-breeding it with grasses
from South Africa.
I could go on and on. Each of you could
think of a dozen great scientific break-
throughs in agriculture that I have not
mentioned, discoveries that helped
change the course of history at least to
some extent. We who are close to Amer-
ican agriculture know the value of our
scientific accomplishments and it is only
human if we should wish that our work
be more appreciated. Beyond a doubt,
the delicately balanced forces of our
world are more stable today because
American agriculture is producing
enough to export $20 billion worth of
urgently needed farm products in the
world markets. That alone should
generate appreciation from the _ pre-
dominantly nonfarm-oriented segment of
our society. I can’t help wondering if the
Same stabilizing effect would result if
some other country were supplying these
femeeds.
Still, we do not seek appreciation so
that we may hear praise. We seek it,
_ father, so that when Americans assess
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
the role that they must play in solving
the problems of tomorrow, they will
realize the full worth of the tools they
already possess. Certainly, the miracle of
American agriculture is among America’s
and the world’s most potent implements
for good.
We in America cannot begin to absorb
the full productivity of our agriculture.
American farmers now are setting pro-
duction records in nearly every major
crop almost routinely. Yet consumers in
the United States, on an annual basis,
use only 40% of the wheat, less than half
the rice, one-half the soybeans, 60% of
the tobacco, two-thirds of the cotton and
three-fourths of the corn the American
farmers produce. Our successful agricul-
tural system demands markets beyond our
borders. That part of our production
which is not used at home is exported
for cash to meet the needs of customers
abroad, rather than being stored as
surplus, which was the unfortunate dis-
position of much of our production in
years past. Today, the markets are there
and I am convinced they will expand,
with fluctuations, in the years ahead.
American agriculture is a miracle today
because the scientists and farmers of
yesterday found the answers to yester-
day’s problems and more. There was a
time, in the early years of this nation,
when “‘going west’’ solved the problem
of infertile soil. When the white man first
came to this land of promise, he cleared
land and worked it until he had drained
it of its nutrients. As productivity de-
clined, he moved on. Then he cleared
more land or plowed up the native grass
and started farming in his new location.
Americans repeated this process until
finally there were no new lands left to
settle. Yields per acre sank lower and
lower as fertility declined. As they faced
an ever-growing population, Americans
saw their geographical frontiers suddenly
restricted by two oceans and the borders
of Mexico and Canada.
They turned to the new frontiers of
increased production. With the intro-
duction of the cotton gin, cotton produc-
tion in the South soared from 10,500 bales
133
in 1793 to 4% million bales in 1861. Steel
and polished iron plowshares were de-
veloped to open the heavy, sticky soils
of the prairie. The mechanical grain
reaper multiplied the harvests. A revolu-
tion was underway on American farms
in the 1800s, just decades after the politi-
cal revolution freed us as a Nation to
pursue our own destiny. It was the
beginning of the modern miracle of
American agriculture.
In their wisdom, our leaders in 1862
created the U. S. Department of Agricul-
ture, ‘‘the general designs and duties of
which shall be to acquire and to diffuse
among the people of the United States
useful information on subjects connected
with agriculture in the most general and
comprehensive sense of that word, and
to procure, propagate, and distribute
among the people new and valuable seeds
and plants.’’ The same year, the Congress
passed the Morrill Act, which established
our uniquely successful Land Grant
University system. A hundred years ago
this year, another significant step was
taken in Connecticut—the first State
Agricultural Experiment Station was
opened.
At this point, nearly all of the ingre-
dients of the miracle were in place. Later
(in 1887), the Hatch Act provided for a
nationwide system of State Experiment
Stations, and (in 1914), the Smith-Lever
Act created the Cooperative Extension
Service. Both moves were immeasurably
successful and key contributors to the
American agricultural miracle. Then and
later, farmers found they needed all the
help they could get just to stay even in
the face of world surpluses, depressed
prices and competition. Now, a more
demanding (though no less competitive)
world benefits from the successes of the
system we created.
From the beginning, the challenges to
our system have been real. But we grew
stronger, rather than weaker, as we met
them. As recently as in 1970, our agricul-
tural science community was tried and
proven strong. That was the year the
corn blight Helminthosporium maydis
struck the corn crop of the United States
134
and reduced it 20-25%. But we had a
scientific team put together that could
stop the blight in its tracks within a short
period of time. Within 24 months we had
a bountiful supply of blight resistant corn
seed. The episode, however, gave us a
warning. It reminded us—scientists,
farmers, and government employees
alike—of the danger of widespread
dependence upon plants which are genet-
ically uniform. Find a disease that can
kill one such plant and you could wipe
out the entire crop of a nation, we were
reminded.
Our American agricultural system is the
miracle of the modern world, but it is
not without problems. When the scientist
brings a new and shiny tool of production
to the farmer, for instance, there have
been times when the farmer felt he could
not afford to employ it. With the scien-
tist’s previous help the farmer may have
produced a record crop, but the prices
he received for that production may have
been discouragingly low. Fortunately,
with new and expanded markets at home
and abroad today, the prices of farm
products have brought returns that cover ~
the cost of modern agricultural tech-
nology. Traditionally, farmers have been
limited in the use of new technology by
low prices.
The American farmer has entered into
a new day of well-being, with all-time
highs set in net income—$29¥% billion in
1973; $27.7 billion in 1974 and an esti-
mated $25 billion this year. With this has
come a great surge in crop production
per acre and more efficient production
of livestock and livestock products.
Previously, for several years, farm
income in the United States fluctuated
between $11 billion and $17 billion, and
$2 to $4 billion of that came out of the
pockets of American taxpayers as a
subsidy.
Because of today’s favorable climate
and an encouraging outlook for marketing
in the future, most of the fruits of research
available today have been adopted by
farmers. It is imperative that new tech-
nology be developed for ready use when
the marketplace demands it. What are
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976 |
some of those needs, as we see them
today?
A meeting of scientists, farm leaders
and interested others in Kansas City,
Mo. in July indicated which direction
we must take. Energy is the field which
should claim our first priority in research,
the conference decided. The agricultural
scientist’s interest in energy spans a wide
area, from strip mining to photosynthesis,
from reduced tillage to frozen foods.
Farming uses only 2.8 percent of the total
fuel consumption in the United States,
but there is always room for improvement
in efficiency. The science-farmer team
has already made fuel savings on reduced
or no-tillage operations common through-
out the United States. But a further 20%
reduction in tillage by 1980 could reduce
fuel requirements for tractors by about
425 million gallons that year alone. Partly
offsetting this, of course, might be the
increased use of energy to produce more
pesticides and more _ reduced-tillage
equipment.
Strip mining could become a major
problem in the northern Great Plains as
the Nation strives to find substitutes for
foreign-produced oil. About 45% of the
Nation’s coal reserves are in the Dakotas,
-Montana and Wyoming and the terrain
invites intensive strip mining. But unlike
the East, where the mine spoil material
is highly acidic, a big problem in the West
is the high concentration of salts in the
spoil material. Research findings so far
are beginning to form the basis of a
technology for returning vast areas of the
northern plains to productive agriculture
after coal extraction. Researchers, for
instance, believe that the four-wing
saltbush may be a promising native
browse plant economically useful for
Teclamation of spoil surfaces. Sheep,
cattle, antelope and deer like it, too.
The second highest priority for re-
_ Search assigned by the Working Con-
ference to Meet U.S. and World Food
~ Needs was increased soybean produc-
_ tion. Soybeans, one of our most important
crops, have stubbornly resisted research
efforts to increase yields. The average
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
yield per acre was 20.1 bushels in 1955
while this year it is an estimated 28.4
bushels. Soybean research has taken
many approaches to the problem already,
with physiologists probing the photosyn-
thesis route and nutritionists seeking
ways to make the plant use fertilizer
nitrogen more efficiently. Other re-
searchers are seeking clues by studying
the overall relationship between plant
and nematodes, one of the great natural
enemies of soybean production.
The third priority area for research
assigned by the conference was the more
efficient use of water for agricultural
production. The problem is as old as
agriculture itself and promises no let-up
in the future. For one thing, if the coal
mined in low rainfall regions of the West
were to be processed there, considerable
quantities of water might be required,
perhaps competing with agricultural
needs in some localized areas.
The conference decided the fourth
priority should be assigned to research
on basic problems in plant growth and
production, while fifth priority should go
to the determination of the nutrient re-
quirements of people. Beyond those, a
wide range of other potential research
subjects were listed in descending order
of priority. These weren’t the decisions
of scientists alone or of farmers alone or
of consumers alone. Spokesmen for
farmers, ranchers, food processors, con-
sumers, marketing firms, nutritionists,
farm organizations, labor unions, inter-
national development experts, environ-
mentalists and federal and state re-
searchers attended that conference.
The setting of priorities on such a scope
shows us surely that the miracle of
American agriculture continues to thrive
and grow strong.
American agriculture continues to
meet its challenges. Farmers can look
forward to continuing good years ahead,
though occasional bad years will creep in
because of poor weather or low prices.
More than ever, successful farmers will
continue to need the fruits of research. I
am confident they will get them.
135
Experiences of an Engineer,
Who Happens To Be a Woman
Carol J. Lehtola
Agricultural Engineer, University of Maryland, College Park, Md. 20742
ABSTRACT
The Equal Employment Opportunity laws see to it that women can get employment
in the engineering field; however, getting a job is only a small part of it. Women in
engineering face several problems and challenges—some subtle, some blatant—that
are discussed.
General Attitudes
‘‘Engineers who are women’’ and
‘‘women engineers”’ are not one and the
same. Therein lies the key to the biggest
problem and challenge facing women in
the engineering field today.
An engineer is a person who applies
scientific principles to practical ends as
the design, construction, and operation
of efficient and economical structures,
equipment, and systems to solve the prob-
lems of our time and improve our stand-
ard of living. Engineers have several
traits in common, among which are: The
ability to solve problems, an interest in
mathematics and science, and an urge to
make creative use of their intelligence. Is
it necessary to mention that these traits
cannot be defined as either masculine or
feminine, but rather as ‘‘personine’’?
However, society presents these as
masculine traits and discourages women
from using their intelligence by expecting
them to avoid responsibility, decision
making, and competition, and by under-
rating their ability. This was expertly
summed up in the February issue of the
Reader’s Digest in Dr. David Reuben’s
article, ‘‘The Marriage Game.’’ Dr.
Reuben states, ‘‘A whole mythology has
been developed; through endless jokes
and cartoons, about women who crumple
fenders, burn dinners, can’t balance the
checkbook and spend all their time play-
ing bridge with the girls. There are, un-
136
fortunately, no cartoons or jokes featur-
ing the women who don’t do these
things, but who hold down full-time jobs,
create gourmet meals and when the day is
over, become provocative companions.”’
Thirty-three percent of Russia’s en-
gineers are women, 1% of America’s
engineers are women. Are American fe-
males less intelligent than Russia’s, or is
it due to the fact that in Russia, a woman’s
intelligence is accepted and utilized? It
is unfortunate that this country continues
placing numerous social stigmas on the
intelligence of women rather than utilizing
this vast intellectual potential.
When a man makes a career choice of
engineering, choosing a career for which
he is suited is the only thing he must
resolve. However, a woman is faced with
two items of concern—that of choosing a
career (which in itself goes against the
norm of society); and that of resolving
the inner conflict of doing something that
is considered masculine and consequently
the fear of not being accepted in the career
for which one’s abilities are best suited.
Women who are in engineering are usually
of strong character, tend to be more stub-
born, and are not afraid of going against
the accepted norm of society.
Once a woman is in the engineering
profession she may encounter some ob-
stacles. These obstacles are a result of
the attitudes—some subtle, some bla-
tant—that have developed from the
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
:
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:
}
mythology about women. Engineers who
are women are too often looked upon as
women engineers, thus all the social stig-
mas are attached. Consequently, we have
an intelligent person who is fully capable
of solving problems, being creative and
dedicated; however, she cannot be given
full responsibility and a decision-making
position, since she is a woman.
Let us examine some of these myths,
connotations, and prejudices:
Longevity in the Work Force
Many employers feel that it’s not worth
the cost and investment of training, etc.
for a woman since she will drop out of the
work force in a short time to raise a family.
Isn’t that a decision to be made by the
woman, not her employer? When an em-
ployer hires a man he has no guarantee
as to how long he will stay there. If a
woman has made it through engineering
school and into the business world,
chances are pretty good she’s not going
to give up her career too easily.
It is also said that a woman will put her
family first; certainly a man should too!
Many women successfully combine
career and family. An excellent example
of this was Dr. Lillian Moller Gilbreth,
a very prominent woman in the field of
industrial engineering and management.
She also happened to be the mother of
twelve children—which is recounted in
the book, ‘‘Cheaper By the Dozen.”’
Travel |
Many women are denied the travel
which may be necessary for their job
or for their career development since it is
felt they may not be able to fend for them-
selves. Anybody who can get through
engineering school is perfectly capable
of riding on an airplane, renting a car,
following directions, and carrying a suit-
_ case. Any person who can drive in the
rush-hour traffic of our asphalt jungles
to work every day should be just as safe
attending an engineering conference in
Chicago or Los Angeles.
Travel is even more frowned upon if a
_man from the office must also go on the
_ J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
trip. In this situation a woman takes with
her a suitcase containing the taboos and
fears of society which are amplified by the
attitudes of co-workers and wives.
Influence
It is frequently stated that ‘‘women
subtly influence men.’’ The irony of this
statement is that for a woman this is con-
sidered to be a bad characteristic and is
detrimental; whereas if a man has this
trait, it is known as leadership.
Women are having an influence on the
engineering field as a whole by ‘‘soften-
ing’’ its image. People are beginning to
realize that engineers work in decent en-
vironments and solve challenging prob-
lems rather than just tramping around at
construction sites in hip boots and hard
hats.
Management
It is usually stated that women can’t
be promoted to management since men
won’t work for women. This goes back to
society’s stigma of men being superior
and women inferior. People work for
people and engineers work for engineers.
To be a manager one must be competent
in the profession, have self-confidence,
and be able to cooperate with others. One
must also be compassionate, under-
standing, and tactful. These are traits
which, again, can’t be attributed as
specifically masculine or feminine, but
personine.
Personal Experiences
An agricultural engineer is an engineer
who applies the principles of engineering
to agricultural problems such as soil and
water conservation, waste management,
power and machinery, food processing,
farm structures, and energy conservation.
The combination of growing up on a
farm, being interested in soil conserva-
tion, and liking math and science led me
to select agricultural engineering as my
career. During the summers (between
college terms) I gained work experience
by working as a student trainee engineer
with the USDA-Soil Conservation Serv-
137
ice. I was fortunate in that they did not
deprive me of field work (one of the
reasons I chose agricultural engineering
was to be able to work outside); however,
they did ask if I wanted to do field work,
whereas for a man this is taken for
granted.
Being an engineer who happens to be
a woman has at times had its problems.
Such things as convincing the profes-
sional societies’ mailing lists that it’s
Mrs., not Mr.; thatif I am to be an officer,
if I’m good enough to be a secretary, why
not president?; when surveying in the field
and climbing up and down gullies, pants
will split; yes, Ican carry my own transit;
and yes, I can change a flat tire!
A frequent problem is that the people
with whom I work will tend to assume
what I want to do, rather than let me make
my own decisions, especially when it
comes to achoice between desk work and
field work. They will assume (rather than
ask) that I’d prefer to do the desk or lab
work. ,
I worked in industry for a year and en-
countered a major obstacle. My manager
refused to give me any challenging work
or anything that may require training since
he had the attitude that “‘women only
have a career of about seven years.”’
He also was the very protective father
image and wouldn’t let me stand on
my own two feet, lest I fall. Needless
was that his manager was a very compe-
tent engineer who happened to be a
woman.
Fortunately, I find the engineer just out
of college is more capable of compre-
hending working with or for an engineer
who is a woman, than does a man who has
been on the job for 40 years. The younger
engineer is more likely to have had girls
in his engineering classes and after awhile
just takes it for granted that women can
138
be engineers. For example, if a female
told my husband she was an engineer
he’d probably just say, ‘“what’s unusual
about that?’’ Considering only 1% of
America’s engineers are women, he is
in a unique position—he is married to an
engineer, and in the group of six engineers
with whom he works, two are women.
Personally, I think engineering is a
good field for a woman. I am satisfied
with the career I selected and find it
challenging and rewarding. It’s a career
that trains a person to think and reason
things out. This aspect of engineering is
important, no matter where you are or
what you do.
Conclusion
Recruiting efforts, etc. are beginning
to make an impact, and girls with an in-
terest in math and science are starting
to consider engineering as a career choice.
In 1975 about 820 women were obtaining
engineering degrees in the U. S. and
about 1,000 are anticipated for the cur-
rent year.
As more women become successful in |
the engineering field, the stigmas should
gradually ebb away. The challenges and
problems faced by women in the profes-
sional fields are dynamic—they are con-
stantly changing. The law protects
women as far as employment goes— only
time, patience, competence, and success
will be able to fully remove the myths
and ‘‘old husband’s tales’’ that go with ©
being a woman. |
Let us stress the term good engineer, |
regardless whether man or woman. |
The most important thing that can be
done for women in engineering is to
emphasize the fact that they are engineers
who happen to be women, rather than
emphasizing women engineers.
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
PROFILE
Benjamin Franklin, American Physicist*
Raymond J. Seeger
National Science Foundation (Retired), 4507 Wetherill Road, Bethesda, MD 20016.
Benjamin Franklin, called the first true
American, was born on January 17th
(NS) 270 years ago in the seaport town of
Boston, soon to become the cradle of
American liberty. His father, a tallow
chandler, was an emigré from England;
his mother, a Folger from Nantucket. He
was baptized across the street from his
home in the puritanical Old South meet-
ing house, where colonial patriots would
later congregate; a pragmatic freethinker,
a deist, he would be buried alongside his
Anglican common-law wife, Deborah
Read, in the Christ Church burial ground
in Philadelphia. Despite his inability to
marry his landlady’s daughter, owing to
the disappearance of her husband, and
her desire not to accompany him on his
sojourns abroad, he had a strong sense of
family ties and obligations, verging on —
nepotism; he early acknowledged publicly
his premarital illegitimate son William and
included him in his household.
When eight years old he entered the
one-room grammar school that later be-
came the Boston Latin School; two years
later he became its most famous dropout.
Self-educated, he received at 47 an
honorary M.A. from Harvard and from
Yale, at SO one from William and Mary,
‘Based on ‘‘Benjamin Franklin: New World
Physicist’’ by Raymond J. Seeger (Pergamon,
Oxford, 1973). This paper is written to celebrate
Franklin’s birthday in the Bicentennial year.
__ J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
at 53 an honorary LL.D from St.
Andrews (hence the appellation doctor)
and at 56 an honorary D.C.L. from
Oxford.
At twelve he was apprenticed to his
brother James, who published one of the
two Boston journals. Five years later he
ran away from Boston, which now boasts
a statue in his honor in front of its City
Hall, to metropolis Philadelphia, later to
become the capital of a new nation.
Penniless, he entered this city, which
now has a commemorative statue atop
its postoffice center. He worked there
and temporarily in London as a journey-
man printer. At 22 he opened his own
printing shop; two years later he became
the official printer for the Pennsylvania
Assembly. Personally ambitious, indus-
trious, and shrewd, he was able to retire
wealthy at 42 from active service. On a
statue in Washington, D.C., the front
bears the inscription Printer; his will
began, ‘‘I, Benjamin Franklin, Printer.’’
On the right side is inscribed Philan-
thropist, on the left Philosopher, and on
the back Patriot. A many-sided person-
ality, nevertheless he was an integrated
person.
At 16 he wrote letters under the
pseudonym of Silence Dogood for his
brother’s newspaper; seven years later he
himself started publishing the ‘‘Pennsyl-
vania Gazette’’ (later named the ‘‘Satur-
day Evening Post’’) and at 27 the annual
139
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ee
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Fig. 1. Benjamin Franklin at 56 (M. Chamber-
lain, Metropolitan Museum of Art).
39
‘Poor Richard: an Almanack,’’ written
by a fictitious Richard Saunders. At 65,
during a week’s stay at the Twyford home
of his friend Jonathan Shipley, Bishop of
St. Asaph, he wrote Part I of a literary
classic for his son, his celebrated ‘**‘Auto-
biography’’ (Part II was begun at the age
of 78, Part III completed at 82, Part IV
unfinished). He wrote simply about the
daily concerns and intimate thoughts of
the first fifty years of the life of a self-
made man; it was not published until
1868. Later he was regarded as the best
writer in 18th-century America; some
even claim that he established the so-
called style of American literature.
A city man of affairs, he was active in
promoting the public welfare; he him-
self had a flare for organizing. He seemed
to be guided by Poor Richard’s apothegm
of 1857. *‘The noblest question in the
world is, ‘What good may I do with it?’ ”’
With nine leather-apron companions at 21
he formed the Junto, a society for mutual
improvement. To facilitate its activities
he organized four years later a Library
Co. (at the time of his death he had the
140
best and largest (4,000 volumes) private
library in the colonies); he himself was an
avid reader. At 30 he helped to form the
voluntary Union Fire Co.; in 1752 he was
instrumental in organizing a Fire Insur-
ance Co. At 31 he was appointed
Philadelphia postmaster; sixteen years
later he became a royal-appointed deputy
postmaster general of North America and
at 69 was elected the first postmaster
general by Congress. At 37 he proposed a
society for promoting useful knowledge,
which led to the founding of the American
Philosophical Society; upon its reor-
ganization in 1769 he became the first
president of this prestigious national
group. At 43 he became president of the
public Academy of Philadelphia (for —
practical education) which developed
subsequently into the University of
Pennsylvania. At 49 he assisted the ill-
equipped forces of General Edward
Braddock in procuring transportation and
helped to organize defense against
marauding Indians who were wont to
prey upon the peace-loving Quakers and
German settlers. The following year he
promoted the formation of a volunteer
Philadelphia militia. At 81 he was still
busy with organizations—for example,
he then helped form a Society for Political
Enquiries and was elected president of a
Society for the Abolition of Slavery. A
common man, he remained a man of the
people throughout his whole life; he was a
true philanthropist, a lover of man and a
promoter of the general welfare. No
wonder he was affectionately called *‘the
sage of Philadelphia,’’ a modern wise
man.
Franklin’s industry was productive not
only in his professional trade and in his
social philanthropy but also in his
amateur science. The generic term philo-
sophy at that period included natural
philosophy, what we nowadays call
physical science. Franklin had a per-
sistent curiosity about such natural
phenomena; he had an innate desire to
understand them and an ingenious ability
to ferret out their secrets as well as to
make use of their properties. He did not,
however, have sufficient leisure to enjoy
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
a -
performing experiments until he retired at
41, when he became inquisitive about
electrostatic phenomena, which were
popular as fashionable demonstrations at
that time. His own observations over the
next four years were compiled as an
English book on *‘Experiments and Ob-
servations on Electricity’’ (no American
edition was published until 1941).
Up to that time only four basic facts
were known about electricity; one theory
had been proposed to explain them. In the
first place, as early as the 6th century
B.C. the attraction of amber for light
materials had been recorded by Thales,
one of the seven wise men of Greece.
Other substances with the same property
were noted through the ages; they were
said to be electric, i.e., like amber (Greek
electron), as distinct from non-electrics
which did not exhibit such a condition
when rubbed. Early in the 17th century a
second fact was discovered, namely, the
repulsion of light objects after making
contact with an electrified body; it was
observed by the Italian Jesuit Nicolo
Cabeo. The French scientist Charles F.
de C. du Fay inferred in 1733 that there
are two electric fluids contained in each
body (like water in a sponge) that would
be released by friction; one resinous (like
rubbed amber), the other vitreous (like
rubbed glass). In the 17th century Otto
von Guericke, a German physicist, was
the first to note that such an electric effect
could be transmitted to some degree by a
linen thread. This third property, the
conduction of electricity (a term intro-
duced about 1646 by the English phy-
sician Sir Thomas Browne), was investi-
gated by the Charterhouse pensioner
Stephen Gray: conductors turned out to
be the non-electrics; insulators, electrics.
Electricity did behave like a fluid. One of
his spectacular experiments (1730) was
repeated in 1744 at Philadelphia by a
lecturer, Archibald Spencer: an electric
Spark was drawn from the nose of a sus-
pended boy whose feet had been rubbed
with a piece of glass. The fourth fact was
the possibility of storing electricity. The
Dutch natural philosopher Pieter van
Musschenbroek, who in 1750 advised
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
Franklin ‘‘to study nature, not books,’’
was shocked in 1746 when he tried to
store some electric charge in a phial con-
taining a gun barrel in water (he had
grasped the gunbarrel with one hand and
the phial with the other). The resulting
Leyden jar (partly coated on the inside
and on the outside with tin foil) became
popular for demonstrating electric dis-
charges—a glorious entertainment, as
when in Paris a charge was passed
through Carthusian monks, lined up
hand-in-hand 900 feet. It is not surprising
that at this very time Franklin became
fascinated by these new electric phe-
nomena. Fortunately, the field was un-
cultivated and could be made productive
with simple experimental techniques
(mathematics, a Franklin weakness, was
not then a prerequisite). It should be
borne in mind that Franklin himself was a
skilled craftsman, adept at handiwork.
Probably his greatest scientific contribu-
tion was his design of crucial experiments
for testing hypotheses.
In 1746 the Library Co. had received a
greenish glass tube for electric use from
its London agent, Peter Collinson, a
Quaker mercer and botanist. Franklin re-
ported his own findings, beginning in
1747, to Collinson in letters. The very
first one begins with the following
experiment. Two persons each stand ona
cake of wax (an insulator). The first
person rubs a glass tube which causes a
spark to jump (no contact) to the second.
Both appear electrically charged to a
third person standing nearby on the floor.
If the first two persons touch each other,
neither will be finally electrified. Franklin
offered a simple explanation. Assume
that the rubbed glass has an excess of a
single electric fluid and then some of it is
transferred by a spark to the second
person. The net result is a deficiency of
the electric fluid for the first person, an
excess for the second; contact neutralizes
their differences—an implicit assump-
tion of the conservation of electric
charge. The normal amount of electric
fluid is an uncharged body is neutral in its
electric effect. Franklin designated an
excess as a positive electric charge, a
141
Fig. 2. Franklin electric machine (American
Philosophical Society).
deficiency as a negative one. This one-
fluid theory requires only electricity and
matter, not two kinds of electricity and
matter. An unresolved problem, how-
ever, was the apparent repulsion of
matter without electric fluid (i.e., nega-
tively charged), whereas matter per se
exhibits only gravitational attraction.
Both theories were then adequate to
explain known electric phenomena—a
dilemma arising from the study of the
conduction of electricity in metals. A
second dilemma arose later through
Michael Faraday’s investigation of the
conduction of electricity in certain
liquids. . Electrolytic results could be
simply explained by the supposition of
atomic ionic carriers each with an integral
number of positive or negative charges.
Were there discrete units of electric
charges or were the carriers themselves
limited to integral capacities? Was
electricity a continuous fluid or essen-
tially atomic in structure? The answer to
both these dilemmas was latent in the
neglected field of the conduction of
electricity in gases. It had to await the
1897 discovery of the negative electron
by Sir Joseph J. Thomson, who regarded
142
Franklin as ‘‘a physicist of the first rank.”’
Both theories were partly right and partly
wrong; there are two electric charges,
but only one moves in a metal, the nega-
tive electrons. (The generally accepted
direction of an electric current is that of
the motion of the positive charge, oppo-
site the actual motion of the electron
current—linguistically confusing, but no
more so than speaking of the rising and
setting sun.)
Franklin found that a conductor could
be given a permanent charge (opposite)
by induction (no contact) and then
grounding it. He was thus enabled to
explain the behavior of a Leyden jar,
which was found to have equal but
opposite charges inside and outside, 1.e.,
a condenser. In 1755 he observed that a
cork suspended in an electrified silver can
was neither attracted nor repelled by the
walls (cf. Faraday’s famous _ice-pail
experiment in 1843). Later his friend the
Unitarian minister and chemist, Joseph
Priestley, who came to Northumberland,
Pennsylvania, in 1794, correctly inferred
(1766) from this fact the existence of an
inverse-square law of force between
relatively small electrified bodies—the
beginning of a quantitative outlook in
electricity.
Undoubtedly Franklin’s most spec-
tacular scientific success was his experi-
mental confirmation of the hitherto
speculation about the relation of electric
sparks to atmospheric lightning. The
basis for his thinking was his recognition
of the peculiar discharge by pointed
conductors, called to his attention by his
coworker, the lawyer Thomas Hopkin-
son. Franklin compared the two phe-
nomena: in twelve respects they were
similar. Accordingly he designed a criti-
cal test; in 1749 he was satisfied and
wrote in his notebook, ‘‘Let the experi-
ment be made!’’ Some members of the
Royal Society of London laughed at his
notion when it was reported by Collin-
son (1750). The French, however, took
the idea seriously. At the suggestion of
the naturalist George L. le Clerc, Comte
de Buffon, the botanist Thomas F.
Dalibard succeeded on May 16, 1752, in
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
drawing electricity from a (charged)
cloud during a clap of thunder by means
of a 40-foot iron rod erected vertically in
a Marly-la- Ville garden just outside Paris.
The experiment was successfully re-
peated the following week in Paris by
M. Delor. Meanwhile, apparently waiting
for the completion of Christ Church
steeple and unaware of the European
work, Franklin performed a modified
experiment with a kite flying on a wet
string, probably with his 21-year old son
on the outskirts of Philadelphia, away
from any skeptical spectators. Electricity
was induced by a nearby (charged) cloud
on a metal point protruding from the
kite; it was conducted by the string to a
key attached to the end. Here Franklin
was able to produce a spark when his
knuckle was brought near it—obviously
not a lightning bolt, otherwise he would
have been killed as was the less fortunate
Swedish physicist, George W. Richmann,
who was struck dead in experimenting
Fig. 3. Franklin electric machine (Franklin
Institute of Philadelphia).
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
" \
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ANN |
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Fig. 4. Franklin spark demonstration models.
with a rod at St. Petersburg the year
following. A modern Prometheus, he had
truly stolen fire from the heavens. As the
French finance minister and physiocrat,
Anne R. J. Turgot, stated in a Latin
epigram in 1776, ‘‘Eripuit coelo fulmen
sceptrumque tyrannis’’ (he snatched
lightning from the sky and the scepter
from the tyrant).
A friend of the best scholars in
America, he proved to be a vital link of
communication between the new world
and the old world. In 1753 he became the
first foreigner to receive the coveted
Copley medal awarded by the Royal
Society for the “‘most important scientific
discovery.’ Three years later he was
made a Fellow of that society. In 1772 he
was elected one of the eight foreign
associates of the French Académie
Royale des Sciences (it was 100 years
before another American was so
honored).
Franklin’s curiosity about nature was
not restricted to electrical phenomena.
He was interested in the German pulse
glass, in the variation of thermal absorp-
tion by differently colored fabrics, in the
use of some oils to calm water waves, in
the dependence of the fluid drag of a boat
upon the depth of a canal. He pursued a
funnel-shaped whirlwind of dust in the
Maryland countryside; he associated the
wind blowing from the northeast with a
storm following a path from the south-
west; he ascribed a constant European
‘‘dry fog’’ to volcanic smoke; he identi-
fied the Gulf stream by his daily measure-
ment of ocean temperatures during his
eight month-long trans-Atlantic voyages.
143
Fig. 5. Franklin stove (1795 model—Metro-
politan Museum of Art).
Franklin is more commonly remem-
bered for his practical interests and
utilitarian concerns epitomized in his
1761 comment to his London landlady’s
daughter, Mary Stevenson—‘*What
signifies philosophy that does not apply to
some use?’’—and in his sententious
retort to a disparaging remark about the
Montgolfier brothers’ hot-air balloon
flights — **What is the use of a new-born
baby?’’ We recall his many inventions,
his household gadgets: a flexible catheter
for his ailing brother, bifocal spectacles
for himself, a mahogany armchair con-
vertible into a ladder, a ‘‘long arm’’ for
reaching books on high shelves, a closed
cast-iron stove in lieu of the open-stove
Fig. 6. Armonica (1762).
144
2
seat) (1785— American Philosophical Society).
fireplace, a musical armonica with 37
revolving glass hemispheres—not to
mention his pointed lightning rod, which
George the 3rd regarded as a Whig plot to
attract lightning to government buildings
for their destruction.
Franklin is known most widely for his
successful venture into international
affairs. A colonial patriot, he truly served
his country unstintingly. He began at the
age of 30, when he was appointed clerk
(for 15 years) of the Philadelphia
Assembly. Twelve years later he was
elected to the Philadelphia Council
and within three years an Alderman and
Philadelphia member of the Assembly.
He participated in the Carlisle Pow-wows
(1753) with representatives of the Indian
Confederation of Six Nations—his first
diplomatic mission. The following year
he proposed a similar plan of union at the
Albany Congress. In 1757, at 51, he sailed
to England as a special Assembly agent to
seek military defense and tax relief. Five
years later he returned, only to be sent
back to England within two years. He be-
came an important factor in the defeat of
the Stamp Act in 1766 when, as the voice
of America, he made a major address
Gx
OX—w"Vv—w
Fig. 7. Leather armchair (note folded ladder under
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
during the 11-hour debate by the House of
Commons. Franklin has been regarded
by some as “‘‘one of history’s pre-
eminent diplomats.’’ In addition to his
urbanity and versatility, Franklin found
doors opened to him by virtue of his
scientific prestige, which had preceded
him. Five times he was elected to the
Royal Society Council. On the other
hand, he was persona non grata to
George the 3rd, whose coronation he
attended in 1761; the king, being indif-
ferent to both science and trade, learned
to dislike this colonial patriot more and
more. A political storm arose when
certain letters containing inflammatory
comments by Thomas Hutchison, Gov-
ernor of Massachusetts, were indis-
creetly used by colonial agitators as
evidence for having the governor de-
posed. Franklin publicly admitted on
Christmas day 1773 that he had sent them
to Boston for private circulation. He was
summoned to appear before the Privy
Council two weeks later, when he was
summarily dismissed as deputy post-
master general; the petition for deposal
was rejected. He departed from England
in disgrace on May Sth, 1775, a trip
saddened by news of his wife’s death.
Franklin’s dual role (royal appointee and
colonial agent) had raised doubts on both
sides of the Atlantic as to his true loyalty.
Until the Revolution to be sure, he was a
moderate, attempting reconciliation, but
thereafter there was no question as to his
colonial patriotism.
The day after his arrival, he was elected
a Pennsylvania delegate (its oldest mem-
ber) to the Second Continental Congress.
A year later he was a member of the Com-
mittee that drafted the Declaration of
Independence. He was elected a Pennsy]l-
vania delegate to the Constitutional Con-
vention. At 70 he was appointed one of
the three Commissioners to negotiate
treaties of amity and commerce abroad,
particularly at the French court of the
22-year-old Louis the 16th and the 21-
year-old Marie Antoinette. As he had
been accompanied to London by his son
William, so he now went with the latter’s
illegitimate son, William Temple.
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
‘*A Genie D. Franklin’’
J. Fragonard).
Bigs. 8: (1778—
He received personal acclaim by the
French as a philosopher of the En-
lightenment, due primarily to his scien-
tific achievement. He was more or less
the official representative of American
learning abroad. His reception was
greater than that for any other American
before or after him. He was, indeed, the
first American to attain a truly inter-
national reputation; his scientific prestige
was America’s greatest asset abroad. The
simplicity of his sober attire (wigless, fur
cap) in the country of the romantic J. J.
Rouseau and his ready wit in the city of
the satirist Voltaire endeared him to the
populace. Despite his old age, Franklin
was welcomed also by a galaxy of
intelligent women; in the prevailing
French mood of flirtation he charmed
them with his almost Parisian gallantries
and bons mots. At the same time he
sought to promote the public understand-
ing of remote America. (He never could
refrain from hoaxes; the French novelist
H. de Balzac remarked that Franklin was
the inventor of the lightning rod, the
hoax, and the republic.) The 1777
Saratoga defeat of the English com-
145
mander (and dramatist) J. Burgoyne
turned the tide of French sympathy
toward America. Among his many duties
Franklin recommended various indi-
viduals to Congress; among them were
the 20-year old Marquis de Lafayette and
the Prussian Baron von Steuben, both of
whom became major generals in the
colonial army. Franklin, together with
commissioners John Adams and John
Jay, signed the 1783 peace treaty in Paris.
At 75, Franklin submitted his resignation
but was not permitted to do so by Con-
gress until four years later. Before he
left Paris he served on a French Com-
mission with the physician J. I. Guillotin;
the chemist, A. L. Lavoisier, et al. to
evaluate the claims of the Austran
charlatan physician F. A. Mesmer.
In 1787 he was a member (its oldest) of
the Constitutional Convention. His com-
promise of a bicameral Congress satisfied
both the proponents of equal state repre-
sentation and their opponents, who de-
manded proportionate population con-
sideration—adopted 17 September
146
(Constitution Day) 1787. On September
16, 1788, at the age of 82, Franklin
resigned his presidency of the special
Pennsylvania Convention for ratification
of the Constitution—the last Colony
had approved it. His political career was
ended; two years later he signed a
memorial about slavery, his last act of
public service.
Ever curious and industrious, Franklin
had wistfully hoped to devote his retire-
ment to scientific pursuits, but gout,
bladder stone, and failing eyesight com-
bined to produce a lingering painful ill-
ness. He died April 7, 1790. Four days
later a cortege of 20,000 persons followed
him mournfully from the State House
(later Independence Hall) to the burial
ground.
Our Franklin heritage is his full life as a
wholesome person, who walked rever-
ently in this wonder-full universe, and
who touched his fellow sojourners with a
loving heart and uplifting hands. He had
personal integrity.
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
;
:
:
.
RESEARCH REPORTS
The Correct Identity of Stator bixae (Drapiez)
with Lectotype Designation (Coleoptera: Bruchidae)
John M. Kingsolver
Systematic Entomology Laboratory, LIIBIII, Agr. Res. Serv., USDA. Mail address:
clo U. §. National Museum, Washington, D. C. 20560.
ABSTRACT
Two species of Bruchidae, Stator bixae (Drapiez) from Brazil and French Guiana,
and §. championi (Sharp) found from Costa Rica to Brazil, have been treated as 1 species.
Both breed in seeds of Bixa orellana L. The 2 species are differentiated, and the lectotype
of S. bixae is designated.
An examination of the type-specimens
of Stator bixae (Drapiez) has revealed a
misapplication of the name to a species
now known as Stator championi (Sharp)
described from Panama. A redescription
of the true bixae and designation of the
lectotype is presented, and characters
distinguishing it from championi are
given.
A number of references concerning the
biology of *“‘Bruchus bixae’’ appear in the
literature, and these are discussed at the
end of this paper.
Stator bixae Drapiez
_ Bruchus bixae Drapiez, 1820, p. 120; Gyllenhal
in Schoenh. 1833, p. 32; Pic, 1913, p. 19; Everts,
1923, p. 199.
Bruchidius bixae: Herford, 1935, p. 16.
Acanthoscelides bixae: Blackwelder, 1946, p. 759.
Body length—2.5-2.75 mm; width—1.6-1.8
mm. Integument red to piceous, eyes black;
vestiture of gray, golden, and dark brown fine
setae in variable pattern (Figs. 1, 2).
Body subovate. Head subtriangular, eyes pro-
truding, ocular sinus about one-third length of
eye; frontal carina prominent, frons and clypeus
finely punctate, frontoclypeal suture angulate;
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
segments 4-11 of antenna slightly eccentric.
Postocular fringe narrow, postocular patch of
setae present. Pronotum subconical, lateral margins
straight, disk evenly convex, finely, evenly,
punctate, slightly depressed basally on each side of
and at middle of basal lobe, lateral carina present
only in basal one-third, nearly hidden by vestiture.
Scutellum subquadrate, emarginate apically. Elytra
as long as wide; striae not distorted, shallowly
sulcate, only 2nd and 6th reaching basal margin,
3rd, 4th and Sth beginning basally on a level with
base of scutellum, striae not coalescent apically.
Pygidium in both sexes subtriangular, with 3 large
subbasal yellow-gray spots, vestiture between spots
sparse, becoming denser toward apex. Front and
middle legs unmodified; entire hind coxal face
densely, finely punctate; hind femur bicarinate on
ventral margin, sulcate between carinae, mesal
carina with acute subapical spine preceded by 2 or
3 setose notches, lateral carina sinuate sub-
apically; hind tibia stout, ventral carina ending in
short, acute mucro, lateral carina ending in short
spine, lateroventral carina ending in sinus between
mucro and lateral spine.
Male genitalia (Figs. 3, 4): median lobe broad;
ventral valve triangular, ending in small tubercle;
internal sac armed with acute, flat denticles in
basal 12, with slender spicules in 2 membranous
lateral sacs, and scattered short denticles in apical
half; apex cylindrical, armed with many fine
spicules. Lateral lobes arcuate, flattened, expanded
then attenuated apically.
147
thee tend
2 NEE
< ; <e ;
an BSS tai .
a aS pat 5 a oe
Stator bixae: Fig. 1, dorsal habitus, fully developed pattern; fig. 2, dorsal habitus, teneral pattern;
fig. 3, ¢ genitalia, median lobe, ventral view; fig. 4, ¢ genitalia, lateral lobes, ventral view.
148 J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
Type-locality.—‘‘Bresil.’’ Type-
series (3) in the Institut Royal des
Sciences Naturelles de Belgique, Brus-
sels. Lectotype ¢ here designated with
labels ‘‘Bresil,’’ ‘“‘coll. Dejean, Coll.
Roelofs,’ “‘Bixae Hoffmansegg’’ agree-
ing with original description. My label
‘‘Lectotype, Bruchus bixae Drapiez, by
Kingsolver’’ is attached to this specimen.
Paralectotypes: 2 2 2, same data as for
lectotype, and my labels indicating their
designation are attached.
Stator bixae is known only from
Brazil and French Guiana, but championi
is found from Brazil to Costa Rica. Both
species apparently breed only in the
seeds of Bixa orellana L. (Bixaceae), a
dye and drug-producing plant locally
called annatto, which has a geographical
distribution (probably artificial) from
Mexico to Brazil. Standley (1923) in-
cludes a discussion of the various uses of
its vegetative parts. Bridwell’s biological
notes (1923) apply to championi as deter-
mined by examination of his material in
the United States National Museum of
Natural History; and Champion’s notes
(1923) probably pertain to championi;
but Evert’s description (1923) indicates
that he likely had bixae. Kingsolver
(1970), in transferring the name bixae to
Stator, used specimens now known to
belong to championi, but the placement
of both specific names in Stator is
correct.
Stator championi can be distinguished
from bixae by the broad, dark stripe
bisecting the pronotal disk; the basal
pygidial ornamentation of 3 white patches
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
of setae set in a yellow, transverse band;
and the apical two-thirds of the pygidium
being nearly glabrous except for a very
narrow medial line of setae. The male
genitalia are also distinctive.
I have examined 2 series of S. bixae. In
both series, 2 patterns of dorsal markings
appeared: 1 with an abbreviated elytral
pattern combined with a large basal
thoracic spot (Fig. 2), 2 with a more
developed elytral pattern associated with
paired thoracic spots (Fig. 1), as illus-
trated from the lectotype.
References Cited
Blackwelder, R. E. 1946. Checklist of the coleop-
terous insects of Mexico, Central America, the
West Indies and South America. U. S. Nat. Mus.
Bull. No. 185, part 4: 551-763.
Bridwell, J. C. 1923. The habits of Bruchus
bixae. J. Wash. Acad. Sci. 13: 261-62.
Champion, G. C. 1923. An American Bruchus
introduced in seeds of Bixa orellana. Entomol.
Mo. Mag. 59: 257-258.
Drapiez, M. 1820. Description de huit especes
d’insectes nouveaux. Ann. Gen. Sci. Physiq.
5: 117-123.
Everts, E. 1923. Bruchus bixae Drapiez. Entomol.
Bericht. 9(no. 133): 199-201.
Gyllenhal, L. 1833. In Schoenherr, C. J. Genera
et species curculionidum, cum synonymia hujus
Familiae. Paris 1: 1-681.
Herford, G. M. 1935. A key to the members of the
family Bruchidae (Col.) of economic importance
in Europe. Trans. Soc. Brit. Entomol. 2: 1-32.
Kingsolver, J. M. 1970. A new combination in the
genus Stator Bridwell. Proc. Entomol. Soc.
Wash. 72: 472.
Pic, M. 1913. Coleopterorum Catalogus, Pars 55,
Bruchidae. Junk, Berlin, 74 p.
Standley, P. C. 1923. Trees and shrubs of Mexico.
Contrib. U. S. Nat. Herbar. 23: 517-848.
149
A New Species of Amblycerus from Panama
(Coleoptera: Bruchidae)
John M. Kingsolver
Systematic Entomology Laboratory, IIBII, Agr. Res. Serv., USDA. Mail address:
clo U. §. National Museum, Washington, D. C. 20560.
ABSTRACT
A new species of seed beetle, Amblycerus tachygaliae, destroys seeds of Tachygalia
versicolor Standley and Williams, a large leguminous tree growing on Barro Colorado I.,
Panama. A. tachygaliae is described and figured, and A. subflavidus (Pic) is designated as
a new synonym of A. pollens (Sharp).
Tachigalia versicolor Standley and
Williams is a caesalpinoid leguminous
tree 75—100 feet in height found in rain
forests from Costa Rica to Panama. It
produces great quantities of large, flat,
single-seeded samaras each 6 to 7 cm
long. From fruits collected on Barro
Colorado I., the following new species of
bruchid was reared.
Amblycerus tachigaliae Kingsolver
(Figs. 1—4)
Body length—9.5 mm. Body width—S5.5 mm.
Pronotal length—2.5 mm. Pronotal width—
4.5 mm.
Color.—Integument orange red in following
areas: base of head, apex of clypeus, labrum,
pronotum, elytra, abdomen, calcaria. Piceous
suffused with reddish: prosternum, mesopleura,
anterior portion of metepisternum, fore legs,
antennae. Piceous: mesosternum, metasternum,
middle and hind legs. Vestiture of very fine
grayish hairs evenly distributed over body, those
on orange red portions with golden sheen; pygidium
with faint median line of closely spaced hairs.
Body elliptical, broad, somewhat depressed
above. Head broad, short; eyes strongly pro-
tuberant, moderately incised at antennal insertion,
postocular fringe of hair transverse; frons convex,
vertex and frons finely punctate except along
median; clypeus slightly depressed basally, finely
punctate except on apical margin; labrum impunc-
tate except for basal row of setae; antennal length
equal to width of pronotal base, moderately serrate.
Pronotum trapezoidal, lateral margins moderately
arcuate, apex subtruncate; basal lobe broad,
shallow; fine submarginal sulcus visible for nearly
entire basal margin, in basal third of lateral
margin, and on apical margin except for middle
150
third, this sulcus hooked laterally around insertion
of the 3 acromial setae on antero-lateral angle;
disk finely punctulate with coarser punctures on
slightly flattened lateral thirds of disk. Scutellum
(Fig. 4) quadrate, slightly longer than wide,
trilobed apically. Elytra somewhat depressed
medially, intervals flat, all striae except 6 and 7
free apically. Pygidium nearly flat, oblique,
slightly emarginate in male, evenly rounded in
female. Prosternum narrow before coxae; inter-
coxal process narrow, apex slightly expanded,
contiguous with vertical face of mesosternal lobe,
hypomeron strongly concave, limited laterally by
shiny sulcus. Metasternum slightly depressed along
midline on posterior margin; postcoxal sulcus
complete across midline, continuous with para-
sutural sulcus which extends to posterior margin;
metepisternal sulcus right angled, extending half-
way along pleural suture. Face of hind coxa
densely covered with fine hairs in lateral three-
fourths, sparsely, finely punctate; polished circular
area surrounding trochanteral articulation with
cluster of fine punctures. Hind femur relatively
slender, ventral margin only slightly sinuate; hind
tibia elliptical in cross section, ventral margin not
flattened; outer calcar four-fifths as long as basi-
tarsus, inner calcar half as long as outer calcar.
Abdomen unmodified except last ventral sternum
broadly emarginate in male, truncate in female.
Male genitalia.—Median lobe (Fig. 2) short,
rather broad; ventral valve broadly triangular,
lateral margins emarginate, dorsal valve semi-
circular apically, narrower at base than ventral
valve; internal sac near apical orifice with paired
lunate sclerites each with a coarse, granular
posterolateral facet, middle of sac with an elongate,
forked sclerite, and a pair of flat, serrate,
curved blades. Lateral lobes as in Fig. 3.
Holotype. — 6, Panama: Barro Colo-
rado I., Feb. 1975, Robin Foster, coll.,
reared from seeds of Tachigalia versicolor
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
Amblycerus tachygalia. Fig. 1, habitus, dorsal view; fig. 2, ¢ genitalia, median lobe, ventral view, with
dorsal view of forked sclerite; fig. 3, ¢ genitalia, lateral lobes, ventral view; fig. 4, scutellum.
Standley & Williams.
#72813.
Allotype.— 2, Panama: Barro Colo-
rado I., 24-II-1975, T. L. Erwin, coll., at
light. In USNMNH Collection.
Paratype.— 6, Panama: Barro Colo-
rado I., 10-III-1961, J. M. Campbell,
coll., at light. In Canadian National
Collection, Ottawa.
USNM Type
Amblycerus tachygaliae is most
Closely related to A. pollens (Sharp)
(=A. subflavidus (Pic), NEW SYN-
ONYMY). The abdomen in A. pollens is
entirely black (red in A. tachygaliae), the
hind femur is lobed on the medioventral
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
carina (straight in A. tachygaliae), the
ventral margin of the metepisternum has
a fusiform, polished, finely ribbed boss
(absent in A. tachygaliae), and marked
differences are present in the ¢ genitalia.
The two species are of comparable size
and are the largest species in Amblycerus
I have seen. The host plant of A. pollens
is not known.
References Cited
Pic, M. 1902. Description de coléoptéres nouveaux.
Bruchidae de |’Amerique meridionale. Natura-
liste 24: 172.
Sharp, D. 1885. Biologia Centralia-Americana,
Insecta, Coleoptera, Bruchidae 5: 437-504.
151
ACADEMY AFFAIRS
THE AWARDS PROGRAM OF THE ACADEMY
AND RECENT HONOREES
Five research scientists and two
science teachers were recipients in the
Spring of the Academy’s awards for out-
standing scientific achievement. The pre-
sentations were made at the Annual
Awards Dinner meeting of the Academy
on Thursday, March 18, 1976, at the
Cosmos Club.
The following research investigators
were honored: Dr. Julius E. Uhlaner
(U. S. Army Research Institute for the
Behavioral and Social Sciences) for Be-
havioral Sciences; Dr. Wayne A. Hend-
rickson (U. S. Naval Research Labora-
tory), for Biological Sciences; Dr. Gerard
V. Trunk (U. S. Naval Research Labora-
tory) for Engineering Sciences; Dr.
Charles H. Johnson (University of Mary-
Julius E. Uhlaner
152
land), for Mathematics; and Dr. William
K. Rose (University of Maryland), for
Physical Sciences.
In the area of Teaching of Science,
the Awardee at the college level was Dr.
Peggy Dixon of the Montgomery College
Faculty. The recipient of the Berenice
G. Lamberton Award for the Teaching of
High School Science was Ms. Edith G.
Durie of the West Springfield High School
faculty.
Behavioral Sciences
Dr. Julius E. Uhlaner, - Chief Psy-
chologist of the U. S. Army and Tech-
nical Director of the Army Research
Institute for the Behavioral and Social
Sciences, and Adjunct Professor of Psy-
chology at George Washington Univer-
sity, was cited for ‘‘his outstanding tech-
nical direction and leadership in Applied
Psychology.’’ As a psychologist, he is
best known for contributions to military
psychology, having spent the major part
of his career as a civilian research
psychologist in the Army. However, he
also kept closely in touch with academia
and industry. He is best known for some
of his innovative contributions to the
Army, having developed the first psy-
chological military qualifications test
legislated by Congress; introduced the
use of the computer as a major tool and
partner in Behavioral Science research;
pioneered night vision testing research
and driver research; introduced the first
differential classification system based on
psychological aptitude testing anywhere
in the military services; pioneered the
‘*system measurement bed,’ a method-
ology which influenced the field of in-
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
dustrial psychology; and fostered the
interdisciplinary approach to much of
his research. Also, he has exhibited very
active professionalism, including the
holding of elective offices in divisions of
the American Psychological Association.
His awards in the Federal service in-
clude the Citation for Meritorious Civilian
Service, 1960; Citation for Exceptional
Civilian Service, 1969; and Citation for
Outstanding Performance, 1972.
Dr. Uhlaner pursued a course of train-
ing and education in science, statistics,
and graduate psychology. While earning
his doctorate at New York University,
he established a driver research labor-
atory. Later, he became associated with
industry. It is this combination of
experience and education which has led
to his trademark for the conduct of re-
search in the Behavioral Sciences—an
interdisciplinary approach, systems or-
iented, and the utilization of research
products.
In addition to his having been elected
a Fellow of the Washington Academy of
Sciences in 1963, he is also a Fellow of
the American Psychological Association.
Also, he is a Fellow of the Human Fac-
tors Society and the Iowa Academy of
Sciences. Other learned societies of
which he is a member are Operations
Research Society of America, Interna-
tional Association of Applied Psychology,
Psychonomics Society, and District of
Columbia Psychological Association.
Biological Sciences
Dr. Wayne A. Hendrickson, Labor-
atory for the Structure of Matter, U. S.
Naval Research Laboratory, was cited
for ‘‘his significant contributions to
knowledge of the structure of the active
sites of oxygen-carrying molecules.’’ He
was born in Spring Valley, Wisconsin.
His B.A. degree was completed in 1963
at the University of Wisconsin (River
Falls). His Ph.D. degree in Biophysics
was conferred by The Johns Hopkins
University in 1968. Dr. Hendrickson was
a postdoctoral fellow at Johns Hopkins
for another year before being awarded
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
Wayne A. Hendrickson
an NRC Postdoctoral Research Associ-
ateship at the Naval Research Labora-
tory in 1969. Professional societies to
which he belongs include the American
Crystallographic Association and the
American Society of Biological Chemists.
His research interests are concerned with
the structure and function of biological
macromolecules as revealed by X-ray
crystallography. Since 1971, Dr. Hend-
rickson has been a Research Biophysicist
in the Laboratory for the Structure of
Matter at the Naval Research Labora-
tory, Washington, D. C.
Engineering Sciences
Dr. Gerard V. Trunk, U. S. Naval Re-
search Laboratory, was cited for ‘‘his
contributions to theory and practice of
processing radar signals in clutter.”
Dr. Trunk was born in Baltimore, Mary-
land on May 9, 1942. He received the
B.E.S. and Ph.D. degrees from The Johns
Hopkins University in 1963 and 1967,
respectively. Since his graduation in 1967,
he has been employed by the Radar
Division of the Naval Research Labora-
tory, Washington, D. C. During the 1974
—1975 academic year, he was on sab-
batical leave and taught at The Johns
Hopkins University.
His research areas are signal detection,
153
Gerard V. Trunk
estimation theory, and pattern recogni-
tion. He has done considerable work in
the area Of sea clutter return from high-
resolution radars. This work entailed
understanding the basic nature of high-
resolution sea clutter, finding a statistical
description of it, and of generating an
optimal detector. At the present time,
he is involved in developing tracking
systems for radar data supplied by mul-
tiple radars located either on the same
ship or on different ships.
Dr. Trunk is a member of Sigma Xi,
Tau Beta Pi, and Eta Kappa Nu.
Mathematics
Dr. Charles H. Johnson, University of
Maryland, was cited for ‘“‘his outstanding
contributions in matrix theory, stability
and eigenvalue location.’’ The theory of
matrices, or linear transformations, is a
field of broad applicability within mathe-
matics as well as to the sciences gen-
erally. Dr. Johnson’s primary interests
within matrix theory include eigenvalue
location, stability matrices and the
numerical range, entry-wise nonnegative
and stochastic matrices, and Hadamard
products. The numerical range is the set
of all values taken on over the surface
154
of the unit ball by the quadratic form of a
matrix. Dr. Johnson is also interested in
the relation of such aspects of matrix
theory to mathematical economics and
modelling, discrete dynamical systems
such as those of demography, and to
combinatorial mathematics.
He was born in Elkhart, Indiana on
January 28, 1948. Dr. Johnson received
his B.A. degree from Northwestern Uni-
versity in 1969 and his Ph.D. in mathe-
matics and economics from the California
Institute of Technology in 1972. From
1972 to 1974, he was an NAS—NRC post-
doctoral research fellow in the Applied
Mathematics Division at the National
Bureau of Standards. In 1974, he came
to the University of Maryland, where he
is now an Assistant Professor. Also, he
serves as a Consultant at the National
Bureau of Standards and as a Visiting
Staff Member at the Los Alamos Scientific
Laboratories. He has served as a Visiting
Lecturer for the Society of Industrial and
Applied Mathematics and also as an in-
vited speaker at meetings of the Amer-
ican Mathematical Society and Mathe-
matical Association of America. He is the
author of more than 40 research papers.
Charles H. Johnson
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
Physical Sciences
Dr. William K. Rose, University of
Maryland, was cited for his *‘important
contributions to our understanding of
highly evolved stars.’’ He was born in
Ossining, New York on August 30, 1935.
Dr. Rose received the A.B. and Ph.D.
degrees from Columbia University in
1957 and 1963, respectively. He was a
research scientist at the U. S. Naval Re-
search Laboratory from 1961 to 1962 and
at the Department of Astrophysical Sci-
ences at Princeton University from 1963
to 1967. In 1957, he joined the M.I.T.
Physics Department, where he held the
positions of Assistant Professor and of
Associate Professor. Since 1971, Dr.
Rose has been an Associate Professor in
the Department of Physics and Astron-
omy at the University of Maryland.
Dr. Rose’s research has included early
work on masers, radio astronomy, and
infrared astronomy from balloons. Since
1965, he has worked on a number of prob-
lems in theoretical astrophysics. Most of
his theoretical research has been con-
cerned with the physical properties and
evolution of stars. Dr. Rose has de-
veloped theories relating to the evolu-
William K. Rose
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
Peggy Dixon
tion of the sun, the origin of planetary
nebulae and novae, X-ray emission
from compact objects, pulsar radiation,
and the physical state of the in-
teriors of red giants and neutron stars.
Recently, Dr. Rose has investigated
several problems in the field of plasma
astrophysics.
Teaching of Science
(College Level)
Dr. Peggy Dixon, Montgomery College,
was cited for “‘improving, and gaining
recognition for, local and national com-
munity college science teaching.’’ She re-
ceived her A.B. degree from Western
Reserve University and her M.S. and
Ph.D. degrees in Physics from the Uni-
versity of Maryland. Memberships in
scientific organizations include the fol-
lowing: American Association of Physics
Teachers (Member-at-large of Executive
Board, 1973-1976; Vice-President of
Chesapeake Section, 1976— ; Represen-
tative to Metric Education Committees,
1974— ; Chairman, Panel on Physics in
Two-year Colleges (PPT YC) of the Com-
mission on College Physics, 1968-1970);
National Science Teachers Association;
155
Edith G. Durie
American Association for the Advance-
ment of Science; American Association
of University Professors; Sigma Xi; and
Sigma Pi Sigma.
Her professional experience includes
three years as Research Associate,
University of Maryland, and fifteen years
at Montgomery College, teaching Mathe-
matics and Geology as well as Physics
and Physical Science.
Some significant educational projects
with which she has been associated are
the following: Resource Packet Project of
PPTYC; NSF—COSIP Grant, Co-Direc-
tor, for articulation in all sciences be-
tween the University of Maryland and all
Maryland Community Colleges, 1970
— 1974; development and teaching of two
honors courses at Montgomery College
(as a member of the Honors Program
Committee over a period of ten years).
Teaching of Science
(High School Level)
(The Berenice G. Lamberton Award)
Ms. Edythe G. Durie, West Springfield
High School, was cited for ‘‘being an out-
standing science teacher who is suppor-
tive of the student on and off the campus.”’
She was born June 3, 1915 in Hellier,
Kentucky. Ms. Durie received her A.B.
degree from Marshall University in 1937
and her M.S. degree from the Graduate
School of Medicine, University of Penn-
sylvania, 1942. She has also done graduate
study at the University of Kentucky and
at the University of California.
From 1942 to 1952, she was supervising
bacteriologist for the Virginia Depart-
ment of Agriculture. Later, she taught
at Hopewell High School, Hopewell,
Virginia, and at the Orleans American
High School in Orleans, France. In
1961, she came to Fairfax County and
taught at Robert E. Lee High School in
Springfield, Virginia. She transferred to
West Springfield High School when it
opened in 1966. She has been Science
Department Chairman there since 1967.
Professional organizations with which
she has been associated are the following:
National Science Teachers Association;
Virginia Academy of Science; W. S.
Junior Academy of Sciences, Wash-
ington Academy of Sciences; and Joint
Board on Science and Engineering
Education (currently serving as Chairman
of the group.—
Kelso B. Morris, General Chairman
NEW FELLOWS
William W. Cantelo, Research Entomolo-
gist, USDA, in recognition of his contri-
butions to entomology, especially to
insect behavior in response to blacklight
traps and to pheromones. Sponsors:
Floyd L. Smith, Richard H. Foote.
156
Lowell E. Campbell, Project Engineer,
USDA, in recognition of science educa-
tion activities on JBSEE, 1960-65, and
professional contributions to electrical
equipment performance and utilization in
agriculture, including recent establish-
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
ment with Dr. H. M. Cathey, USDA,
that vegetative growth in plants is de-
pendent on level and duration of ra-
diation in the 400 to 850 nm region
without spectral preference. Sponsors:
Hajime Ota, Henry M. Cathey, Milton
S. Schechter.
Satya D. Dubey, Chief, Statistical Eval-
uation Branch, Bureau of Drugs, Food &
Drug Adm., in recognition of his contri-
butions to mathematical statistics and in
particular to his publications on Weibull
and other distributions. Sponsors:
Grover C. Sherlin, Joan R. Rosenblatt,
Nelson W. Rupp.
Alan O. Plait, Principal Staff Engineer,
Computer Sciences Corp., in recognition
of his extensive educational programs in
training persons in the mathematical arts
and sciences for application to engineer-
ing and quality assurance problems and
for his work in transfering the technology
of the assurance sciences to new fields
such as housing and environmental
problems. Sponsors: Grover C. Sherlin,
Joan R. Rosenblatt, Nelson W. Rupp.
James M. Schalk, Research Entomolo-
gist, USDA, in recognition of contribu-
tions in entomology, particularly on
developing host plants resistant lines of
forage and vegetable crops to arthropod
pests. Sponsors: Floyd L. Smith, Richard
H. Foote.
Herbert H. Snyder, Prof. Mathematics,
Southern Ill. Univ. at Carbondale, in
recognition of his contributions to elec-
tromagnetic theory and in particular
to the mathematical theory of propaga-
tion of electromagnetic waves in periodic
_ Structures and the interactions of such
waves with beams of charged particles;
and for his contribution to the theory of
regular functions on linear associative
algebras. Sponsors: Joan R. Rosenblatt,
_ Florence H. Forziati.
_Manya B. Stoetzel, Research Entomolo-
_ gist, USDA, in recognition of her contri-
bution to the biosystematics of scale
insects, and in particular to her studies
on the life histories and the adult male
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
and immature stages of the aspidiotine
scales. Sponsors: Richard H. Foote,
Louise M. Russell, R. R. Colwell.
Howard E. Waterworth, Research Plant
Pathologist, US Plant Introduction Sta-
tion, Glenn Dale, Md., in recognition of
his contributions to Plant Pathology,
especially in the field of virology and
serology. Sponsors: Floyd L. Smith,
H. Ota, Richard H. Foote.
Sajjad H. Durrani, Senior Engineer,
Goddard Space Flight Ctr., in recognition
of his contributions to the conceptual
design and analysis of space communica-
tion systems. Sponsors: Edward Wolff,
George Abraham, Emanuel Brancato.
Lloyd Knutson, Chairman, Insect Iden-
tification and Beneficial Insect Intro-
duction Institute, ARS, USDA, in rec-
ognition of his outstanding research
contributions to the systematics and
taxonomy of snail-killing flies and his
leadership as Chairman of ARS’s Insect
Identification & Beneficial Insect Intro-
duction Institute at Beltsville. Sponsors:
Richard H. Foote, Louise M. Russell,
Ashley H. Gurney.
Kendall G. Powers, Research Parasitolo-
gist, NIH, in recognition of his contribu-
tions in the field of chemotherapy and
immunology of parasitic diseases; par-
ticularly malaria and schistosomiasis.
Sponsor: James H. Turner.
Roger H. Lawson, Research Pathologist,
USDA, in recognition of his contribu-
tions to an understanding of viral cause
and identity of diseases of orchids and
chrysanthemums, and of his studies on
ultrastructural cytology and the develop-
ment of inclusion bodies associated with
plant virus infection. Sponsors: Henry
M. Cathey, Lloyd F. Smith.
Ralph E. Webb, Research Entomolo-
gist, USDA, in recognition of his contn-
butions in entomology, especially his
research on the biology and control of
insect pests of ornamentals and vegetable
crops, also induced and natural resist-
ance of plants to insect attack. Sponsors:
Floyd L. Smith, Richard H. Fooie.
157
Armand B. Weiss, Director, Systems
Integration, Federal Energy Adm., in
recognition of his contribution to opera-
tions research, in particular his research
on quantitative aspects of policy level
decision making, his research leading to
improved economic models of logistic
support processes, and his significant
contributions to modelling the national
energy needs, distribution and resources.
Sponsors: John Honig, Jean K. Boek.
Robert L. Gluckstern, Chancellor, Uni-
versity of Maryland, in recognition of
his scientific contributions to high energy
physics and his design of cyclotrons.
Sponsors: Joseph M. Marchello, S. N.
Foner.
SCIENTISTS IN THE NEWS
Contributions in this section of your Journal are earnestly solicited.
They should be typed double-spaced and sent to the Editor three
months preceeding the issue for which they are intended.
HARRY DIAMOND LABORATORIES
Frank Reggia has received an Army
R & D achievement award for his pi-
oneering efforts and outstanding accom-
plishments in the design, development
158
and demonstrated use of a novel group of
conformal antennas for military systems.
These high performance antenna designs
are capable of eliminating many mechan-
ical and electrical problems while en-
hancing overall system performance. The
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976 |
antennas are constructed as an integral
part of a body, at any position along its
length and flush with the surface.
Born in Northumberland, PA, Frank
married the former Betty Jo Patterson of
Clarksville, Arkansas in 1945. The couple
| have two sons James Allen, 26, and Daniel
Lee, 22, and currently reside in Bethesda,
MD. Frank has attended George Wash-
ington University and the University of
Maryland majoring in Engineering and
Physics. In 1970 he earned a BS (cum
laude) and in 1971 a MS from Bucknell
University, both in electrical engineering.
He isa member of Tau Beta Pi, a National
| Engineering Honor Society; a Fellow,
Institute of Electrical and Electronic
Engineers; a Fellow, American Associ-
| ation for Advancement of Science; and a
| Fellow, Washington Academy of Scien-
ces. In addition, he is the author of 50
_ technical articles in the microwave field,
and holds 16 patents on microwave ferrites
and acoustic components.
NATIONAL BUREAU OF STANDARDS
|
| Dr. Florence Forziati, President-Elect,
_Washington Academy of Sciences, pre-
sented a scroll commemorating the 75th
anniversary of NBS to Dr. Ernest Ambler,
Acting Director, NBS, on March 4, 1976.
Dr. Ambler’s acknowledgment follows:
Dear Dr. Forziati:
|
I wish to express my appreciation to you for
the beautiful commemorative scroll from the
Washington Academy of Sciences which you
_ presented to the Bureau yesterday, on the oc-
_ casion of our 75th birthday.
I am sure that the Bureau and its staff members
will continue in the future, the close relationship
with the Academy which has existed so many
years in the past.
I think it was especially appropriate that the
__ presentation be made by you, because of your
employment for so many years at the Bureau
as a scientist.
_ Sincerely,
Ernest Ambler
Acting Director
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
NATIONAL INSTITUTES OF HEALTH
David B. Scott has been named Direc-
tor of the National Institute of Dental
Research. Dr. Scott was dean of the
School of Dentistry, Case Western Re-
serve University.
‘Dr. Scott . . . brings to this post an
outstanding background in dental re-
search, education, and administration,”’
said Dr. Donald S. Fredrickson, NIH
Director.
The new NIDR Director joined the fac-
ulty of Western Reserve University in
1965 as the Thomas J. Hill Distinguished
Professor of Physical Biology in the
School of Dentistry and was jointly ap-
pointed as professor of anatomy in the
School of Medicine. Following the feder-
ation of the University with the Case
Institute of Technology to form Case
Western Reserve University, Dr. Scott
became dean of the School of Dentistry
in 1969.
Dr. Scott, whose appointment was ef-
fective Jan. 1, has returned to NIH,
where he served from 1944 to 1965.
He was with the Dental Section,
Division of Physiology, Experimental
Biology and Medicine from 1944 until
1948, when the NIDR was established,
and he served as chief of the Institute’s
Laboratory of Histology and Pathology
from 1956 to 1965.
Dr. Scott received the B.A. degree in
physical biology from Brown University
in 1939 and his D.D.S. from the Baltimore
College of Dental Surgery, University of
Maryland, in 1943. The next year he was
awarded the M.S. degree from the Uni-
versity of Rochester where he was a
Carnegie Fellow. In 1956, he received
one of the awards given the 10 most out-
standing young men in Government serv-
ice by the Arthur S. Flemming Awards
Commission.
Dr. Scott was cited for his develop-
ment of new methods for applying the
electron microscope to the study of en-
amel and dentin, and the development of
new techniques for studying the structure
of teeth. Other awards accorded Dr.
Scott include: honorary membership,
159
Finnish Dental Association; honorary
lecturer, Tokyo Dental College, and the
International Association for Dental
Research Award for Research in Miner-
alization, 1968. 7
Dr. Scott is a Fellow, American
Association for the Advancement of
Science, a Fellow, the American College
of Dentists and the International College
of Dentists; and a Fellow, Washington
Academy of Sciences.
He has served in scientific posts
with the Federation Dentaire Interna-
tionale.
He is a member of the Electron Micro-
scope Society of America, the American
Dental Association, and is president of
the International Association for Dental
Research.
NATIONAL OCEAN SURVEY
Hyman Orlin, author, teacher, mathe-
matician, and geodesist, has retired after
more than 33 years of service with the
Federal government. Orlin, who leaves
the post of Chief Scientist of the National
Oceanic and Atmospheric Administra-
Hyman Orlin
160
tion’s National Ocean Survey, will be-
come Senior Scientist with the National
Academy of Sciences in Washington,
D. C., later this month.
————
A recognized authority in the field of ©
geodesy, Orlin has been with NOAA’s
National Ocean Survey and its pred-
ecessor, the Coast and Geodetic Survey,
since 1947 when he was employed as
mathematician. In 1969, he was ap-
pointed Special Assistant to the Director
for Earth Science Activities as the prin-
cipal advisor in geophysical matters.
Orlin has represented NOAA at Inter-
national Astronomical Union Symposia,
since 1958. He has served as Co-Chair-
man of the Sea Bottom Surveys Panel of
the U. S.-Japan Natural Resources
Committee, and has held discussions ©
with Japanese officials on international
cooperative programs and the exchange
of scientists. He is an authority on the
geodetic aspects of offshore boundaries
and Law of the Sea and serves as advisor
to and member of the U. S. Interagency
Committee on Law of the Sea.
Orlin has taken an active role in inter-
governmental agency efforts which have ~
resulted in improved services and prod-
ucts for the general public. He has served
as president of the Geodesy Section of the
American Geophysical Union, and has
received the coveted Silver Beaver
Award for his contribution to Boy Scout-
ing. In 1970, he was presented the
Heiskanen Geodesy Award from Ohio
State University where he had received
his doctorate in geodetic science in 1962.
As an author, Orlin has published num-
erous scientific articles on his gravity
observations, geodetic astronomy, geo-
physics, law of the sea and the earth’s
external gravity field. He has taught grad-
uate and undergraduate courses in geo-
detic sciences at George Washington
University and is coordinator for the
Geodetic and Cartographic Science and
the Oceanographic Science programs at
the University.
A native of New York City, Orlin has |
received degrees from the City College
of New York, George Washington Uni-
versity, and Ohio State University. He |
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
and his wife, the former Lenore Driller .
of Bronx, N. Y., live in Silver Spring, Md.
He is a member of Sigma Xi and the Inter-
national Astronomical Union and a Fel-
low of the American Geophysical Union
and the Washington Academy of
‘Sciences.
NAVAL RESEARCH LABORATORY
Dr. Isabella L. Karle received the
American Chemical Society’s 1976 Gar-
van medal and $2,000 on April 5 during
the Society’s Centennial meeting in New
York City.
Dr. Karle was named to present the
award address this year on April 8 at a
symposium arranged by the Biochem-
istry Division of the ACS. Among the
speakers at this symposium was _ her
daughter, Dr. Louise Karle Hanson, a
spectroscopist at the National Institute
of Health. Coincidentally, Dr. Karle,
who is also president of the American
Crystallographic Association, presented
greetings from that society to the ACS
at a ceremonial session, along with the
presidents of many other scientific
societies from the United States and
around the world. .
An authority in x-ray crystallography,
Dr. Karle has developed a practical pro-
cedure to determine molecular structures
of complex substances, including mate-
rials of biological and medical interest,
that previously could not be studied by
x-ray techniques. Before she introduced
her method, the direct method of phase
determination, scientists were limited to
restricted types of compounds that could
be examined by x-ray crystallography
-—the best technique to determine the
three-dimensional atomic arrangement in
a molecule. In particular, compounds of
biological interest, because they are
composed of lightweight elements, were
not amenable to the x-ray technique. Dr.
Karle’s method changed that.
_ Dr. Karle is recognized for her struc-
tural investigations employing the new
method. She has elucidated structural
features in antibiotics; radiation damage
to genetic material; heart drugs; drug
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
antagonists; frog venoms; compounds
induced by ultraviolet radiation and
associated with primary visual response;
and ion-transport in biological systems.
A native of Detroit, she received the
B.S. in 1941, the M.S. in 1942, and the
Ph.D. in 1944 at the University of
Michigan, completing the doctorate at the
age of 22. She remained at the Uni-
versity of Michigan as an instructor in
chemistry until 1946, when she joined the
Naval Research Laboratory as aresearch
physicist. Author of more than 100
papers on electron and x-ray diffraction
studies of crystal and molecular struc-
tures, Dr. Karle has supervised several
programs of postdoctrol research and
maintains collaborative research proj-
ects with government laboratories and
research institutions throughout the
world.
Honors accorded Dr. Karle are the
Navy Superior Civilian Service Award
(1965), the Naval Research Laboratory’s
Scientific Research Society of American
Applied Science Award (1967), the
Society of Women Engineers Annual
Achievement Award (1968), the Hille-
brand Award of the American Chemical
Society’s Washington section (1969), the
Federal Woman’s Award (1973), and
membership in Phi Beta Kappa and
Sigma Xi.
She is a fellow of the Washington
Academy of Sciences, an honorary life
member of the Society of Women
Engineers, and a member of the U. S. A.
National Committee for Crystallography,
the American Crystallographic Associa-
tion, the American Physical Society,
the American Chemical Society, the
American Association for the Advance-
ment of Science, the Biophysical Society,
the Research Society of America, and the
Advisory Board of the publication
Biopolymers, an international journal
of research on biological molecules.
In addition to the honorarium and the
gold Garvan Medal, Dr. Karle received
a bronze replica of the medal. The award
was established in 1936 through a dona-
tion from Francis P. Garvan and is sup-
ported by a fund set up at that time.
161
OBITUARIES
Norman H. C. Griffiths
Norman H. C. Griffiths throughout
his professional career served his family,
Howard University, and the world. He
was a Skilled prosthodontist, educator,
researcher, and humanitarian. Dr. Grif-
fiths passed away quietly on June 22,
1976 in the Howard University Hospital
after a lengthy illness. He would have
retired from his faculty position at the
University on June 30, 1976 after 28 years
of full-time service.
Dr. Griffiths graduated from the
Howard University College of Dentistry
in 1947 with honors. He received his
graduate education at Northwestern Uni-
versity, where he earned the M.S.D.
Degree in 1948 and at the University of
Pennsylvania where he received his
diploma in Prosthetic Dentistry in 1953
and the Doctor of Science Degree in
1957. He was first appointed to the
dental faculty of Howard University in
1948 as an Assistant Professor.
During his very active career in teach-
ing and dental practice, he spent many
hours devoting his professional services
to hospitals in the Washington area and
lecturing to state, national, and local
dental societies throughout the United
States.
Dr. Griffiths has been an ambassador
of health and the College’s international
faculty member. He taught and provided
dental health care in India, Africa,
Egypt, Ceylon, the West Indies and
Europe. He spent 2 tours of duty on the
S. S. Hope—the American Hospital
Ship—where he provided dental serv-
ices in Guinea, West Africa. He subse-
quently served as a consultant and ad-
visor to the Hope staff.
His long list of honors and service
include (President of the Caribbean
American Intercultural Organization;
Visiting Professor, University of Ceylon;
Visiting Professor in India and Egypt on
a U.S. State Department grant; member,
Washington Academy of Sciences; Past
President, Chi Delta Mu fraternity;
162
Past State Vice President, National
Dental Association; Past President, Pi Pi
Chapter, Omicron Kappa Upsilon, the
dental honor society; and the American
Cleft Palate Association. |
Professor Griffiths has made numerous
contributions to the dental literature in
his field of removable prosthodontics.
His articles appear in the Journal of
Dental Research; the Bulletin of the Na-
tional Dental Association; Journal of
Dental Education; Journal of the Ameri-
can Dental Association; Journal of the
D. C. Dental Society, and the Egyptian
Dental Journal.
His scholarly lectures and clinical
expertise in the treatment of patients
with missing teeth and other oral dis-
orders will be missed by his professional
colleagues, the faculty, staff, and stu-
dents of the College of Dentistry. He
has made special contributions to the field
of prosthodontics through advances in
technical and clinical diagnostic pro-
cedures for patients with missing teeth.
Dr. Griffiths is survived by his devoted —
wife Peggy S. and six children: Stephanie
Denise, Dwight Norman, Michael Craig,
Arthur Alexander, Peggy Manel, and
Jacqueline Deneen; one sister, Stephanie
G. Brown; and a host of relatives,
colleagues, and friends.
Marjorie Hooker
Marjorie Hooker, 67, a geologist with
the U. S. Geological Survey for nearly
30 years, died of cancer May 4, 1976.
With the Survey since 1947, she was
responsible for abstracting geological
literature, compiling data on the composi- |
tion of igneous and metamorphic rocks of |
the world, and for international correla- |
tion of chemical data on granitic rocks.
Miss Hooker had received worldwide |
recognition for her work in scientific |
bibliography and for her activities with |
international scientific societies. |
Born in Flushing, N.Y., she was a |
graduate of Hunter College and received
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
a master’s degree in geology from Syra-
cuse University. She took graduate
work at Columbia University.
She worked for 4 years as a mineral
resource analyst with the State Depart-
ment before joining the Geological
Survey.
As organizer of abstracts from Amer-
ica for ‘‘Mineralogical Abstracts’’ since
1969, Miss Hooker had published 64
papers and was an adviser on chemical
data.
She helped organize conferences for
international societies, developed new
programs in mineralogical and petrologic
studies, and corresponded extensively
with geologists all over the world. Miss
Hooker had been a delegate to 4 interna-
tional geological congresses, including
the one in Prague in 1968 that was in-
terrupted by the Soviet invasion.
She was a fellow of the Mineralogical
J. WASH. ACAD. SCI., VOL. 66, NO. 2, 1976
Society of America, the Geological
Society of London and the American
Association for the Advancement of
Science. She also was a member of
the American Geophysical Union, the
American Institute of Mining Engineers,
the Association of Earth Science Editors
and the mineralogical societies of Great
Britain, France, Canada, Switzerland
and Japan.
Miss Hooker, who lived at 2018
Luzerne Ave., Silver Spring, had served
as a judge at area science fairs. She
had been active in the North Woodside—
Montgomery Hills Citizens Association
for 22 years and had served as a trustee
of the Woodlin Elementary School PTA
in Silver Spring.
She is survived by two sisters, Elsie
A. Hooker, of Flushing, and Vera H.
Heidrick, of Addison, N. Y.
163
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VOLUME 66
Number 3
| J Our nal of the SEPTEMBER, 1976
WASHINGTON
ACADEMY... SCIENCES
Issued Quarterly
—, at Washington, DC.
Directory Issue
CONTENTS
Directory, 1976:
Directory of The PNCAGC INNS. Sete sk oe akon s Pa Seren
MIME IICAMOISUINO Meee 2 os ceca we se we eee bbs ae ee
Order form for Tape Cassettes from
Symposium—Energy Recovery from Solid Wastes ...
Washington Academy of Sciences
Founded in 1898
EXECUTIVE COMMITTEE
President
Florence H. Forziati
President-Elect
Richard H. Foote
Secretary a
Nelson W. Rupp
Sa
Treasurer
Mary H. Aldridge
Members at Large
George Abraham
Grover C. Sherlin
BOARD OF MANAGERS
All delegates of affiliated
Societies (see facing page)
EDITOR
Richard H. Foote
EDITORIAL ASSISTANT
Elizabeth Ostaggi
ACADEMY OFFICE
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Washington, D.C. 20014
Telephone (301) 530-1402
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September, and December)—the September issue
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Back Issues
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tom of opposite column): Proceedings: Vols. 1-13 |
(1898-1910) Index: To Vols. 1-13 of the Proceedings |
and Vols. 1-40 of the Journal Journal: Back issues,
volumes, and sets (Vols. 1-62, 1911-1972) and all cur-
rent issues.
Claims for Missing Numbers
Claims will not be allowed if received more than 60 |
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for postal delivery and claim. No claims will be al- |
lowed because of failure to notify the Academy of a
change in address. .
Change of Address
Address changes should be sent promptly to the Aca- |
demy office. Such notification should show both old t |
and new addresses and zip number.
Published quarterly in March, June, September, and December of each year by the
Washington Academy of Sciences, 9650 Rockville Pike, Washington, D.C. Second class
postage paid at Washington, D.C. and additional mailing offices.
DELEGATES TO THE WASHINGTON ACADEMY OF SCIENCES,
REPRESENTING THE LOCAL AFFILIATED SOCIETIES
ERAacapiiicdls SOCIElY Of WaASMIMSTOM ao. c eo ..6 ole Pe nah eee age ee ees ob eee James F. Goff
Paine polorcical Society o£ Washimpstont ee... loess. fee. ee ee ce ee ee ee ee Jean K. Boek
Seee CAMS OCICS VOR VAS MIN GCOMs, cr). cs. cece hee oe wee eidi es sue ele sun cege ces tae seh ess be has Inactive
Me AmSOCICLYy, Ol Washimetones! «tn! 2k seca as «leas LaGas dwindles Delegate not appointed
Eeamalseicalesociety of Washington), 2-252... 02s. osc eee ce eee bbe este cence Maynard Ramsay
eh ee OO LAPIN CLS OCIC UN ns Ce eo. es as ye. has ae ee ee ee T. Dale Stewart
PmMeone ae SOCIcty ol WashingtOM 2... 2.0.50. 6 sce cee Jee eee cs ceee ee Marian M. Schnepfe
MemeEsocienzo the Distictior Columbia”... . 0.2.00 62. cose en eet ptm ence e sens cseeeues Inactive
PNA DH CAM HISTORIC SOCICUY = oie coe) o cerc ist as te ses b gid viele to Wael wie Sl viale aug eis Slee bres Paul H. Oehser
Pec ESOcictyeoO! WashimetOn, ... 06.6 access qmes sees ot woe ete Sp ea mec e ew dese snes Conrad B. Link
PeecmmOle Mine miCan FOLESUCTS).. 2225.5. .6 ekeG eh lelds bia ea dlba as oe ee cas we lees Thomas B. Glazebrook
ESPERO TOMESOCICIV TON MH MOINGCES . <2. 20 eke aces eet) et wef ee we dees cae core Oo ele George Abraham
Pmunteeoielectiical and Electronics Engimeers ................00.00 0 PBR ees wees George Abraham
PinMcMtcanmSOcieny on Mechanical BNOMEES 45.65. 6 ccc es tee eee bene sees usaweus Michael Chi
Ammo occa Society Of WaShiNgtOMi ... 4.26. oid cue ce ens oe eee ve wee eee Robert S. Isenstein
PieMecanESOciety 1OL, Microbiology tsa le. Weed One Tk eh le lo Se ee a als Delegate not appointed
Meroe AMeM cam Military EMPITCENS, .....6 00 onda ec 6 aes gba ys ves ns oe ee cae eae eee H.P. Demuth
AUSSI SOGISIY Cie Crk IN Bo (2410 Vee) he eee ee Shou Shan Fan
Seicw mone xpenmental Biology and Medicine ..........5 60.0.0. c0ccscnesscgectess Donald Flick
-SPERISAMD SOCISIN] TON G1 I ee ere er ee en ee Glen W. Wensch
International Association of Dental Research nies A RA ae Aatieel base ead Raeaa ener RERE William V. Loebenstein
eimemean Institute of Aeronautics and Astronautics .............. 000 00c cece e cent ees Franklin Ross
aca Met COrOlogzical SOCICLY 65... «<5 net cee OMe ce a eae He ee he le ds A. James Wagner
Reel CESOCIehy Ol WASMINGTON 3 ieee oe ch ce ss oles evens saws agsecseuces Robert J. Argauer
PRUE TESOCICNyCOL AINGIICA 2.5. acer fe tac secu sca ce sent sceeswuss Delegate not appointed
ECL CRIT: INIIGCISRIE SCENE Re else Ae en Dick Duffey
PereMecrOnmsOodmlcchnologists: 012-4. syenuies. Bead aces ed wees Jes Vode William Sulzbacher
Pete AMMO CHANITICESOCCIY er ee ee ee ss de ie inde en eee e eek a vawoe tees Inactive
2 LE SURDELNSIITCall SCTE See ee te Ae tee a Pana Onn ne ane PR Delegate not appointed
DEAGEStOM) TEISUD ROE SCTE ere CUT oes te rite sea Inactive
PeienICAneNSSOCIAtION Ol-Physics: TeaGhers . 2.0.60. 6 cca ee eee bbe ee eee Bernard B. Watson
DCMS OCI OlONINCIIC Aen cere oar ok eset oe bot vs tees hese Gewese ewbieas Ronald W. Waynant
PneMcAnSOciciyaor Plant Physiologists 4 4.h. 226. leds ves see wekdew ose ees Chae Walter Shropshire
PemnooniO perations Research Council) 2). oo5 5)... ee eee ee ke. John G. Honig
PeMMUMCHIASOCICMYAOIO ANI CIRCA EE 6 the a. io 2) pee as hen eat aa en Rie eww eee ee ae ODS Inactive
American Institute of Mining, Metallurgical
ane MOL SUM I OMNIS CTS Memento sae aye eves, AYe¥s esos dc, J) cane dee.) = kos Sets nd ae ewe Carl H. Cotterill
Beeson CapilolvNstonomers: 24098008 .o.. c hee x. eae SPOR UA Delegate not appointed
REMC MICMICAIUNSSOCIANOMOL AMENCA 0.022.206 o0. snc se cae seca eee teceecccvescacce Patrick Hayes
2: LRSEMUIS CHGS ee eR es ee Miloslav Recheigl, Jr.
PS Chol OorcalmASSOCIIEOM A!) as ace be ites ve cet MG bbe be bible sdb be'eee eee eeene John O’ Hare
Peay ashineton) Pant LechmicaliGnroupltcic... 5... 0s. 0 se eee ee cee eee cence nes Paul G. Campbell
Delegates continue in office until new selections are made by the representative societies.
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976 165
us ’ , ‘ en oe i
> — |
_- |
se i Agee
166 J. WASH.
THE DIRECTORY OF THE ACADEMY FOR 1976
Foreword
The present, 51st issue of the Academy’s direc-
tory is again this year issued as part of the Septem-
ber number of the Journal. As in previous years,
the alphabetical listing is based on a postcard
questionnaire sent to the Academy membership.
Members were asked to update the data concerning
address and membership in affiliated societies by
June 30, 1976. In cases in which cards were not
received by that date, the address appears as it was
used during 1976, and the remaining data were
taken from the directory for 1975. Corrections
should be called to the attention of the Academy
office.
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
Code for Affiliated Societies, and Society Officers
The Philosophical Society of Washington (1898)
President: Robert J. Rubin, 3308 McKinley St., N.W., Washington, D.C. 20015
Vice-President: Paul A. Willis, 2824 W. George Mason Rd., Falls Church, Va. 22042
Secretary: James F. Goff, 3405 34th Pl., N.W., Washington, D.C. 20016
Delegate: James F. Goff
Anthropological Society of Washington (1898)
President: Robert Humphrey, George Washington Univ., Washington, D.C. 20037
President-elect: Priscilla Reining, Catholic Univ. of America, Washington, D.C. 20064
Secretary: Mary F. Gallager, American Univ., Washington, D.C. 20016
Delegate: Jean K. Boek, National Graduate Univ., 3408 Wisconsin Ave., N.W.,
Washington, D.C. 20016
Biological Society of Washington (1898)
President: Joseph Rosewater, Smithsonian Institution, Washington, D.C. 20560
Secretary: Richard C. Banks, Smithsonian Institution, Washington, D.C. 20560
Chemical Society of Washington (1898)
President: Robert F. Cozzens, George Mason Univ., Fairfax, Va. 22030
President-elect: David Venezky, Naval Res. Lab., Washington, D.C. 20375
Secretary: John Moody, NBS, Chemistry, Bldg. 222, Washington, D.C. 20234
Delegate: None appointed
Entomological Society of Washington (1898)
President: H. Ivan Rainwater, Rm. 635, Federal Bldg., Hyattsville, Md. 20782
President-elect: George C. Steyskal, W-617, NMNH, Washington, D.C. 20560
Secretary: Theodore J. Spilman, W-605, NMNH, Washington, D.C. 20560
Delegate: Maynard J. Ramsay, Rm. 660, Federal Bldg., Hyattsville, Md. 20782
National Geographic Society (1898)
President: Robert E. Doyle, National Geographic Society, Washington, D.C. 20036
Chairman: Melvin M. Payne, National Geographic Society, Washington, D.C. 20036
Secretary: Owen R. Anderson, National Geographic Society, Washington, D.C. 20036
Delegate: T. Dale Stewart, Smithsonian Institution, Museum of Natural History,
Washington, D.C. 20560
Geological Society of Washington (1898)
President: Joshua I. Tracey, Jr., U.S. Geological Survey, Reston, Va. 22092
Vice-President: Dallas L. Peck, U.S. Geological Survey, Reston, Va. 22092
Secretary: Penelope M. Hanshaw, U.S. Geological Survey, Reston, Va. 22092
Delegate: Marian M. Schnepfe, 2019 Eye St. N.W. #402, Washington, D.C. 20006
Medical Society of the District of Columbia (1898)
President: William S. McCune
President-elect: Frank S. Bacon
Secretary: Thomas Sadler
Delegate: Not appointed
167
9 Columbia Historical Society (1899)
President: Hemer T. Rosenberger, 1307 New Hampshire Ave., N.W., Washington,
D.C. 20036
Vice-President: Wilcomb E. Washburn, Smithsonian Institution, Washington, D.C. 20560
Secretary: Edward F. Gerber, 1233 30th St., N.W., Washington, D.C. 20007
Delegate: Paul H. Oehser, National Geographic Society, Washington, D.C. 20036
10 Botanical Society of Washington (1902)
President: Peter M. Mazzeo, U.S. National Arboretum, 28th & M Sts., N.E.,
Washington, D.C. 20002
Vice-President: Laurence E. Skog, Smithsonian Institution, Dept. of Botany, Washington,
D.C. 20560
Secretary: Erik A. Neumann, U.S. National Arboretum, 28th & M Sts., N.W.,
Washington, D.C. 20002
Delegate: Conrad B. Link, Univ. of Md., Dept. of Horticulture, College Park,
Md. 20742
11 Society of American Foresters, Washington, Section (1904)
President: Thomas B. Glazebrook, 7809 Bristow Dr., Annandale, Va. 22003
President-elect: Arthur H. Smith, 3301 Wessynton Way, Alexandria, Va. 22309
Secretary: George Cheek, American Forest Institute, 1619 Mass. Ave., N.W.,
Washington, D.C. 20036
Delegate: T. B. Glazebrook
12 Washington Society of Engineers (1907)
President: Joseph H. Seelinger, 5367 28th St., N.W., Washington, D.C. 20015
Vice-President: Dean Harold Liebowitz, Sch. of Engineering, George Washington Univ.,
Washington, D.C. 20052
Secretary: Guy S. Hammer, II, 1526 17th St., N.W., #107, Washington, D.C. 20036
Delegate: George Abraham, 3107 Westover Dr., S.E., Washington, D.C. 20020
13 Institute of Electrical & Electronics Engineers, Washington Section (1912)
Chairman: Alvin Reiner, 11243 Bybee St., Silver Spring, Md. 20902
Vice-Chairman: Dennis Bodson, 233 North Columbus St., Arlington, Va. 22203
Secretary: C. David Crandall, 12214 Old Colony Dr., Upper Marlboro, Md. 20870
Delegate: George Abraham, 3107 Westover Dr., S.E., Washington, D.C. 20020
14 American Society of Mechanical Engineers, Washington Section (1923)
Chairman: Darnley Howard, Postal Service Research Institute, Rockville, Md.
Vice-Chairman: Michael Chi, 2721 24th St. N., Arlington, Va. 22207
Secretary: Robert L. Hershey, Booz-Allen Applied Res., Bethesda, Md. 20014
Delegate: Michael Chi
15 Helminthological Society of Washington (1923)
President: Robert S. Isenstein, Animal Parasitology Inst., BARC-East, Beltsville,
Md. 20705
Vice-President: A. Morgan Golden, Nematology Lab., Plant Protection Inst., BARC-
West, Beltsville, Md. 20705
Secretary: William R. Nickle, Nematology Lab., Plant Protection Inst., BARC-
West, Beltsville, Md. 20705
Delegate: James H. Turner, Division of Res. Grants, NIH, Westwood Bldg.,
Rm. A25, Bethesda, Md. 20014
16 American Society for Microbiology, Washington Branch (1923)
President: Joseph C. Olson, Jr., Food & Drug Adm., Washington, D.C.
Vice-President: Charles H. Zierdt, NIH, Bethesda, Md. 20014
Secretary: June W. Bradlaw, Food & Drug Adm., Washington, D.C.
Delegate: None appointed
17 Society of American Military Engineers, Washington Post (1927)
President: Lt. Col. Elton D. Scheideman, HQ USAF/P REN, Washington, D.C. 20330
Vice-President: Capt. Clayman C. Meyers, OICC Bethesda, 200 Stovall St., Naval
Facilities Engrg. Command, Alexandria, Va. 22332
Secretary: Capt. Terry M. Fenstad, HQ USAF/PREV, Washington, D.C. 20330
Delegate: Hal P. Demuth, 4025 Pine Brook Rd., Alexandria, Va. 22310
168 J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
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American Society of Civil Engineers, National Capital Section (1942)
President: L. Gary Byrd, 2921 Telester Ct., Falls Church, Va. 22042
Vice-President: James W. Harland, 1511 K St., N.W., Suite 337, Washington, D.C. 20005
Secretary: John J. Duffy, American Concrete Pipe Assoc., 8320 Old Court House Rd.,
Vienna, Va. 22180
Delegate: Shou-shan Fan, 2313 Glenallen Ave., #202, Silver Spring, Md. 20906
Society for Experimental Biology & Medicine, D.C. Section (1952)
President: Juan C. Penhos, Dept. of Physiology & Biophysics, Georgetown Univ.
School of Med. & Dentistry, Washington, D.C. 20007
President-elect: Cyrus R. Creveling, 4516 Amherst Lane, Bethesda, Md. 20014
Secretary: Marvin Bleiberg, 3613 Old Post Rd., Fairfax, Va. 22030
Delegate: Donald F. Flick, 930 19th St., So., Arlington, Va. 22202
American Society for Metals, Washington Chapter (1953)
Chairman: Klaus M. Zwilsky, U.S. Atomic Energy Comm., Washington, D.C. 20545
Vice-chairman: Alan H. Rosenstein, Air Force Office of Scientific Res., 1400 Wilson Blvd.,
Arlington, Va. 22209
Secretary: Joseph Malz, NASA, Code RWM, Washington, D.C. 20546
Delegate: Glen W. Wensch, U.S. Atomic Energy Comm., Washington, D.C. 20545
International Association for Dental Research, Washington Section (1953)
President: Robert W. Longton, Dental Sciences Dept., Naval Med. Res. Inst.,
NNMC, Bethesda, Md. 20014
Vice-President: Nelson W. Rupp, Dental Res., NBS, Washington, D.C. 20234
Secretary: Donald W. Turner, Dental Sciences Dept., Naval Med. Res. Inst.,
NNMC, Bethesda, Md. 20014
Delegate: William V. Loebenstein, 8501 Sundale Dr., Silver Spring, Md. 20910
American Institute of Aeronautics and Astronautics, National Capital Section (1953)
President: Philip R. Compton, 6303 Mori St., McLean, Va. 22101
Vice-President: Jack Suddreth, Code RLC/Aero. Prop. Div., NASA Headquarters,
Washington, D.C. 20546
Secretary: Paul M. Burris, The Boeing Co., 955 L’Enfant Plaza North, S.W.,
Washington, D.C. 20024
Delegate: Frank J. Ross, Deputy for Rqmts., Off. Asst. Sec. of A.F., The Pentagon,
Rm. 4E973, Washington, D.C. 20330
American Meteorological Society, D.C. Chapter (1954)
Chairman: G. Stanley Doore, NOAA/NWS/TPB/WIIX2, 1302 Gramax Bldg.,
8060 13th St., Silver Spring, Md. 20910
Vice-Chairman: Robert Ellingson, IFDAM, Space Services Bldg., Univ. of Md., College
Park, Md. 20742
Secretary: H. Michael Magil, NOAA/NWS/PSB/WII2X3, 1425 Gramax Bldg.,
8060 13th St., Silver Spring, Md. 20910
Delegate: A. James Wagner, NOAA/NWS/NMC W31, 604 World Weather Bldg.,
5200 Auth Rd., Washington, D.C. 20233
Insecticide Society of Washington (1959)
President: Richard Back, Union Carbide, 1730 Pa. Ave., N.E., Suite 1250,
Washington, D.C. 20006
President-elect: John W. Kennedy, APHIS, USDA, Hyattsville, Md.
Secretary: John Neal, ARS, ARC, Bldg. 467, Beltsville, Md. 20705
Delegate: Robert Argauer, ARS, ARC, Bldg. 309, Beltsville, Md. 20705
Acoustical Society of America (1959)
Chairman: John A. Molino, Sound Section, NBS, Washington, D.C. 20234
Vice-chairman: Charles T. Molloy, 2400 Claremont Dr., Falls Church, Va. 22043
Secretary: William K. Blake, Naval Ship R & D Ctr., Bethesda, Md. 20034
Delegate: None appointed
American Nuclear Society, Washington Section (1960)
President: Andre Gage, Potomac Electric Power Co., 1900 Penn. Ave., N.W.,
Washington, D.C.
Vice-President: B. E. Leonard, Institute for Resource Management, 4948 St. Elmo Ave.
Bethesda, Md. 20014
Secretary: S. Bassett, NUS Corp., Rockville, Md. 20852
Delegate: Dick Duffy, Nuclear Engineering, Univ. of Md., College Park, Md.
20742
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976 169
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Institute of Food Technologists, Washington Section (1961)
Chairman: Tannous Khalil, Giant Foods, Inc., Landover, Md. 20785
Vice-chairman: Florian C. Majorack, Food & Drug Adm., Washington, D.C.
Secretary: Glenn V. Brauner, National Canners Assoc., Washington, D.C. 20036
Delegate: William Sulzbacher, 8527 Clarkson Dr., Fulton, Md. 20759
American Ceramic Society, Baltimore-Washington Section (1962)
Chairman: W. T. Bakker, General Refractories Co., P.O. Box 1673, Md. 21203
Chairman-elect: L. Biller, Glidden-Dirkee Div., SCM Corp., 3901 Hawkins Point Rd.,
Baltimore, Md. 21226
Secretary: Edwin E. Childs, J. E. Baker Co., 232 E. Market St., York, Pa. 17405
Delegate: None appointed
Electrochemical Society, National Capital Section (1963)
Chairman: Judith Ambrus, Naval Surface Weapons Ctr., White Oak, Md. 20910
Vice-chairman: John B. O’Sullivan, 7724 Glenister Dr., Springfield, Va. 22152
Secretary: John Ambrose, NBS, Washington, D.C. 20234
Delegate: None appointed
Washington History of Science Club (1965)
Chairman: Richard G.Hewlett, Atomic Energy Comm.
Vice-chairman: Deborah Warner, Smithsonian Institution
Secretary: Dean C. Allard
Delegate: None appointed
American Association of Physics Teachers, Chesapeake Section (1965)
President: William Logan, D.C. Teachers College, 2565 Georgia Ave., Washington,
D.C. 20001
Vice-President: Eugenie V. Mielczarek, George Mason Univ., 4400 University Dr.,
Fairfax, Va. 22030
Secretary: John B. Newman, Towson State College, Towson, Md. 21204
Delegate: Bernard B. Watson, 6108 London Lane, Bethesda, Md. 20034
Optical Society of America, National Capital Section (1966)
President: James B. Heaney, NASA, Goddard Space Flight Ctr., Greenbelt, Md. 20770
Vice-President: Diane Prinz, Naval Research Lab., Washington, D.C. 20375
Secretary: Marilyn J. Dodge, National Bureau of Standards, A-251, Physics Bldg.,
Washington, D.C. 20234
Delegate: James B. Heaney
American Society of Plant Physiologists, Washington Section (1966)
President: Aref Abdul-Baki, USDA, ARCW, Beltsville, Md. 20705
Vice-President: Dale G. Blevins, Dept. of Botany, Univ. of Md., College Park, Md. 20742
Secretary: Anne H. Datko, NIMH Bldg. 32A, Rm. 101, Bethesda, Md. 20014
Delegate: W. Shropshire, Jr., Smithsonian Institution, 12441 Parklawn Dr.,
Rockville, Md. 20852
Washington Operations Research Council (1966)
President: Frank T. Trippi, 5809 Clermont Dr., Alexandria, Va. 22310
President-elect: Craig C. Sherbrooke, 8513 Kingsgate Rd., Potomac, Md. 20854
Secretary: Neal D. Glassman, 1 Paddock Ct., Potomac, Md. 20854
Delegate: John G. Honig, 7701 Glenmore Spring Way, Bethesda, Md. 20034
Instrument Society of America, Washington Section (1967)
President: Francis C. Quinn
President-elect: John I. Peterson
Secretary: Frank L. Carou
Delegate: None appointed
American Institute of Mining, Metallurgical & Petroleum Engineers (1968)
Chairman: Phil W. Guild, U.S. Geological Survey, Natl. Ctr., Mail Stop 952,
12201 Sunrise Valley Dr., Reston, Va. 22092
Vice-Chairman: Gus H. Goudarzi, U.S. Geological Survey, Natl. Ctr., Mail Stop 920,
12201 Sunrise Valley Dr., Reston, Va. 22092
Secretary: John Patterson, Energy Res. & Dev. Adm., Washington, D.C. 20545
Delegate: Carl H. Cotterill, Bureau of Mines, U.S. Dept. of the Interior, 2401 E St.,
N.W., Washington, D.C. 20241
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
Si)
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National Capital Astronomers (1969)
President: Benson J. Simon
Vice-President: Geoffrey P. Hornseth
Secretary: William R. Winkler
Delegate: None appointed
Maryland-District of Columbia and Virginia Section of Mathematical Assoc. of America (1971)
Chairman: Geraldine A. Coon, Goucher College, Baltimore, Md.
Secretary: John Smith, George Mason University, Fairfax, Va.
Delegate: Patrick Hayes, 5565 Columbia Pike #812, Arlington, Va 22204
D.C. Institute of Chemists (1973)
President: Kelso B. Morris, 1448 Leegate Rd., N.W., Washington, D.C. 20012
President-elect: Leo Schubert, 8521 Beech Tree Rd., Bethesda, Md. 20034
Secretary: Fred D. Ordway, 2816 Fall Jax Dr., Falls Church, Va. 22042
Delegate: Miloslav Rechcigl, Jr., 1703 Mark Lane, Rockville, Md. 20852
The D.C. Psychological Association (1975)
President: Lee Gurel, 2723 Woodley Pl., N.W., Washington, D.C. 20008
President-elect: Richard P. Youniss, 6111 43rd Ave., Hyattsville, Md. 20781
Secretary: Eugene Stammeyer, 419 Timber Branch Parkway, Alexandria, Va. 22302
Delegate: John J. O’Hare, 301 G St., S.W., #824, Washington, D.C. 20024
The Washington Paint Technical Group (1976)
President: Rufus F. Wint, Hercules, Inc., 910 Market St., Wilmington, Delaware 19899
Vice-President: William Georgov, J. M. Huber Corp., P.O. Box 310, Havre de Grace,
Md. 21078
Secretary: Robert F.Brady, Jr., General Services Adm. (FMBP), Washington, D.C.
20406
Delegate: Paul G. Campbell, National Bureau of Standards, B-348 Br., Washington,
D.C. 20234
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976 171
Alphabetical List of Members
M = Member; F = Fellow; E = Emeritus member L = Life Fellow. Numbers in parentheses refer to
numerical code in foregoing list of affiliated societies.
A
ABELSON, PHILIP H., Ph.D., Carnegie Inst. of
Washington, Carnegie Institution of Washing-
ton, 1530 P St., N.W., Washington D.C. 20005
(F-1, 4, 7, 16)
ABRAHAM, GEORGE, M.S., Ph.D., 3107 West-
over Dr., S.E., Washington, D.C. 20020 (F-1,
Gril alaot. Se)
ACHTER, M. R., Code 6416, U.S. Naval Research
Lab., Washington, D.C. 20375 (F-20, 36)
ADAMS, CAROLINE L., 242 North Granada St.,
Arlington, Va. 22203 (E-10)
ADLER, SANFORD C., 14238 Briarwood Terr.,
Rockville, Md. 20853 (M-1)
ADLER, VICTOR E., 8540 Pineway Ct., Laurel,
Md. 20810 (F-5, 24)
ADRIAN, FRANK J., Applied Phys. Lab., Johns
Hopkins Univ., 8621 Georgia Ave., Silver
Spring, Md. 20910 (F)
AFFRONTI, LEWIS, Ph.D., Dept. of Microbiology,
George Washington Univ. Sch. of Med., 2300
Eye St., N.W., Washington, D.C. 20037 (F-16)
AHEARN, ARTHUR J., Ph.D., 9621 East Bexhill
Dr., Box 294, Kensington, Md. 20795 (F-16)
AKERS, ROBERT P., Ph.D., 9912 Silverbrook Dr.,
Rockville, Md. 20850 (F-6)
ALBUS, JAMES S., 6100 Westchester, 1406, Col-
lege Park, Md. 20740 (F)
ALDRICH, JOHN W., Ph.D., 6324 Lakeview Dr.,
Falls Church, Va. 22041 (F-3)
ALDRIDGE, MARY H., Ph.D., Dept. of Chemistry,
American University, Washington, D.C. 20016
(F-4)
ALEXANDER, ALLEN L., Ph.D., 4216 Sleepy
Hollow Rd., Annandale, Va. 22003 (F-4)
ALEXANDER, BENJAMIN, Ph.D., Pres., Chicago
State Univ., 95th St. at King Dr. Chicago Ill.
(F)
ALGERMISSEN, S. T., 5079 Holmes PI., Boulder,
Colo. 80303 (F)
ALLEN, ANTON M., D.V.M., Ph.D., 11718 Lake-
way Dr., Manassas, Va. 22110 (F)
ALLEN, FRANCES, Ph.D. 7507 23rd Ave.,
Hyattsville, Md. 20783 (F)
ALTER, HARVEY, Ph.D., Nat. Center for
Resource Recovery, Inc., 1211 Connecticut
Ave., N.W., Washington, D.C. 20036 (F-4)
ALTMAN, PHILIP L., 9206 Ewing Dr., Bethesda,
Md. 20034 (M)
ANDERSON, JOHN D., Jr., Ph.D., Dept. Aerospace
Eng., Univ. Maryland, College Park, Md.
20742 (F-6, 22)
ANDERSON, MYRON S., Ph.D., 1433 Manchester
Lane, N.W., Washington, D.C. 20011 (F-4)
ANDERSON, WENDELLL., Rural Rt. 4, Box 4172,
La Plata, Md. 20646 (F-4)
ANDREWS, JOHN S., Sc.D., Animal Parasitology
172
Inst., Agr. Res. Cent. (E), USDA, Beltsville,
Md. 20705 (F-15)
ANDRUS, EDWARD D., BS., 1600 Rhode Island
Ave., N.W., Washington, D.C. 20036 (M-7, 25)
APOSTOLOU, Mrs. GEORGIA L., 1001 Rockville
Pike, #424, Rockville, Md. 20852 (M)
APPEL, WILLIAM D., B.S., 12416 Regent Ave.,
N.E., Albuquerque, N. Mex. 87112 (E-6)
APSTEIN, MAURICE, Ph.D., 4611 Maple Ave.,
Bethesda, Md., 20014 (F-13)
ARGAUER, ROBERT J., Ph.D., 4208 Everett St.,
Kensington, Md. 20795 (F-24)
ARMSTRONG, GEORGE T., Ph.D., 1401 Dale Dr.,
Silver Spring, Md. 20910 (F-1, 4)
ARONSON, C. J., 3401 Oberon St., Kensington,
Md. 20910 (M-1, 32)
ARSEM, COLLINS, 10821 Admirals Way,
Potomac, Md. 20854 (M-1, 6, 13)
ASLAKSON, CARL I., 5707 Wilson Lane, Be-
thesda, Md. 20014 (E)
ASTIN, ALLEN V., Ph.D., 5008 Battery Lane,
Bethesda, Md. 20014 (E-1, 13, 22, 31, 35)
AXILROD, BENJAMIN M., 9915 Marquette Dr.,
Bethesda, Md. 20034 (E-1)
AYENSU, EDWARD, Ph.D., 510 H. St., N.W.,
Washington, D.C. 20024
BAKER, ARTHUR A., Ph.D., 5201 Westwood Dr.,
N.W., Washington, D.C. 20016 (E-7)
BAKER, LOUIS C.W., Ph.D., Dept of Chemistry,
Georgetown University, N.W., Washington,
D.C. 20007 (F-4)
BALLARD, LOWELL D., 722 So. Colonial, Ster-
ling, Va. 22170 (F-1, 6, 13, 32)
BARBROW, LOUIS E., Natl. Bureau of Standards,
Washington, D.C. 20234 (F-1, 13, 32)
BARGER, GERALD L., Ph.D., 17 West Blvd. N.,
Columbia, Mo. 65201 (F-23)
BARNHART, CLYDE S., Sr., Rt. 4, Box 207A,
Athens, Ohio 45701 (F)
BARRETT, MORRIS K., Mrs., Ph.D. 5528
Johnson Ave., Bethesda, Md. 20034 (F-7)
BEACH, LOUIS A., Ph.D., 1200 Waynewood
Blvd., Alexandria, Va. 22308 (F-1, 6)
BEASLEY, EDWARD E., Ph.D., Physics Dept.,
Gallaudet College, Washington, D.C. 20002
(F-1)
BECKER, EDWIN D., Ph.D., Inst. Arthritis & Meta-
bolic Dis., Bldg. 2 Rm. 122, National Institutes
of Health, Bethesda, Md. 20014 (F-4)
BECKETT, CHARLES W., 5624 Madison St.,
Bethesda, Md. 20014 (F-1, 4)
BECKMANN, ROBERT B., Dean, College of
Engineering, Univ. of Md., College Park, Md.
20742 (F-4)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
BEIJ, HILDING, K., 69 Morningside Dr., Laconia,
NH. 03246 (L)
BEKKEDAHL, NORMAN, Ph.D., 405 N. Ocean
Blvd., Apt. 1001, Pompano Beach, Fla. 33062
BELLANTI, JOSEPH A., Ph. D., 6007 Carewood
Lane Bethesda, Md. 20016 (F-6, 10)
BELSHEIM, ROBERT, Ph.D., 2475 Virginia Ave.
#514, Washington, D.C. 20037 (F-1, 12, 14)
BENDER, MAURICE, Ph.D., 621 W. Mallon, Suite
201, Spokane, Wa. 99201 (F)
BENESCH, WILLIAM, Inst. for Molecular Physics,
Univ. of Maryland, College Park, Md. 20742
(F-1, 32)
BENJAMIN, C. R., Ph.D., IPD/ARS, USDA, Rm.
459, Federal Bg., Hyattsville, Md. 20782
(F-6, 10)
BENNETT, BRADLEY F., 3301 Macomb St., N.W.,
Washington, D.C. 20008 (F-1, 20)
BENNETT, JOHN A., 7405 Denton Rd., Bethesda
Md. 20014 (F, 20)
BENNETT, MARTIN TOSCAN, Ch.E., 3700 Mt.
Vernon Ave., Rm. 605, Alexandria, Va. 22305
(F-4, 6)
BENNETT, WILLARD H., Dept. of Physics, North
Carolina State Univ., Raleigh, N.C. 27607 (E, 1)
BENSON, WILLIAM, Ph.D., 2101 Constitution
Ave., N.W., Washington, D.C. 20418 (M-32)
BERGMANN, OTTO, Ph.D., Dept. Physics,
George Washington Univ., Washington, D.C.
20006 (F-1)
BERLINER, ROBERT W., M.D., Dean, Yale
School of Medicine, New Haven, Conn. 06510
(F)
BERNSTEIN, BERNARD, M. S., 11404 Rouen Dr.,
Potomac, Md. 20854 (M-25)
BERNTON, HARRY S., 4000 Cathedral Ave.,
N.W., Washington, D.C. 20016 (F-8)
BERRY, Miss ARNEICE O., 5108 Hayes St.,
N.E., Washington, D.C. 20019 (M)
BESTUL, ALDEN B., 9400 Overlea Ave., Rock-
ville, Md. 20850 (F-1, 6)
BICKLEY, WILLIAM E., Ph.D., Dept. of
Entomology, Univ. of Md., College Park,
Md. 20742 (F-5, 24)
BIRD, H. R., Animal Science Bg., Univ. of Wis-
consin, Madison, Wisc. 53706 (F)
BIRKS, L. S., Code 6480, U.S. Naval Research
Lab., Washington, D.C. 20375 (F)
BLAKE, DORIS H., A.M., 3416 Glebe Rd., North
Arlington, Va. 22207 (E-5)
BLANK, CHARLES A., Ph.D., 5110 Sideburn Rad.,
Fairfax, Va. 22030 (M-4, 6, 39)
BLOCK, STANLEY, Ph.D., National Bureau of
Standards, Washington, D.C. 20234 (F-4)
BLOOM, FLOYD E., M.D., Div. Spec. Mental
Health Res., NIH, St. Elizabeth’s Hospital,
Washington, D.C. 20032 (F)
BLUNT, ROBERT F., 5411 Moorland Lane,
Bethesda, Md. 20014 (F)
BOEK, JEAN K., Ph.D., Natl. Graduate Univ., 3408
Wisconsin Ave., N.W., Washington, D.C.
20016 (F-2)
BOGLE, ROBERT W., Code 53071, Naval Res.
Lab., 991 Skylark Dr., La Jolla, Cal. 92037
(F)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
BONDELID, ROLLON O., Ph.D., Code 6640, Naval
Research Lab., Washington, D.C. 20375 (F)
BORTHWICK, HARRY A., 13700 Creekside Dr.,
Silver Spring, Md. 20901 (E)
BOTBOL, J. M., 2301 November Lane, Reston,
Va. 22901 (F)
BOWLES, ROMALD E., Ph.D., 2105 Sondra Ct.,
Silver Spring, Md. 20904 (F-6, 14, 22, 35)
BOWMAN, PAUL W., 3114 5th St. N., Arlington,
Va. 22201 (F)
BOWMAN, THOMAS E., Ph.D., Dept. Invert.
Zoology, Smithsonian Inst., Washington,
D.C. 20560 (F-3)
BOZEMAN, F. MARILYN, Div. Virol., Bur.
Biologics, FDA, 8800 Rockville Pike, Rock-
ville, Md. 20014 (F-16, 19)
BRADY, ROBERT F., Jr., Ph.D., 706 Hope Lane,
Gaithersburg, Md. 20760 (F-4, 41)
BRANCATO, E. L., Code 4004, U.S. Naval Re-
search Lab., Washington, D.C. 20390 (F-4, 41)
BRANDEWIE, DONALD F., 6811 Field Master Dr.,
Springfield Va. 22153 (F)
BRAUER, G. M., Dental Research A-123 Polymer,
Natl. Bureau of Standards, Washington, D.C.
20234 (F-4, 21)
BREGER, IRVING A., Ph.D., 212 Hillsboro Dr.,
Silver Spring, Md. 20902 (F-4, 6, 7, 39)
BREIT, GREGORY, 73 Allenhurst Rd., Buffalo,
N.Y. 14214 (E-13)
BRENNER, ABNER, Ph.D., 7204 Pomander Lane,
Chevy Chase, Md. 20015 (F-4, 6, 29)
BREWER, CARL R., Ph.D., 8113 Lilly Stone Dr.,
Bethesda, Md. 20034 (F)
BRICKWEDDE, F. G., 104 Davey Lab., Dept. of
Physics, Pennsylvania State Univ., University
Park, Pa. 16802 (F-1)
BRIER, GLENN W., M.A., Dept. Atmosph. Sci.,
Colorado State Univ., Ft. Collins, Colo.
80523 (F-23)
BROADHURST, MARTIN G., 504 Blandford St.,
Apt. 4, Rockville, Md. 20850 (F)
BROMBACHER, W. G., 6914 Ridgewood Ave.,
Chevy Chase, Md. 20015 (E-1)
BROOKS, RICHARD C., Ph.D., 6221 N. 12th St.,
Arlington, Va. 22205 (M-13, 34)
BROWN, RUSSELL G., Ph.D., Dept. of Botany,
Univ. of Maryland College Park, Md. (F)
BROWN, THOMAS, McP., S. 25th St. and Army-
Navy Dr., Arlington, Va. 22206 (F)
BRUCK, STEPHEN D., Ph.D., 1113 Pipestem PI.,
Rockville, Md. 20854 (F-4, 6, 39)
BRYAN, MILTON M., 3322 N. Glebe Rad.,
Arlington, Va. 22207 (M-11)
BURAS, EDMUND M., Jr., M.S., Gillette Research
Inst., 1413 Research Blvd., Rockville, Md.
20850 (F-4, 6, 39)
BURGER, ROBERT J., (COL. M.S.) 5307 Chester-
field Dr., Camp Springs, Md. 20031 (F-6, 22)
BURGERS, J. M., Prof., 4622 Knox Road, Apt. 7,
College Park, Md. 20740 (F-1)
BURK, DEAN, Ph.D., 4719 44th St.,
Washington, D.C. 20016 (E-4, 19, 33)
BURNETT, H. C., Metallurgy Division, Natl.
Bureau of Standards, Washington, D.C.
20234 (F)
N.W.,
173
BYERLY, PERRY, Ph.D., 5340 Broadway Terr.,
#401, Oakland, Calif. 94618 (F)
BYERLY, T. C., 6-J Ridge Rd., Greenbelt, Md.
20770 (F)
C
CALDWELL, FRANK R., 4821 47th St., N.W.,
Washington, D.C. 20016 (E-1, 6)
CALDWELL, JOSEPH M., 2732 N. Kensington St.,
Arlington, Va. 22207 (E-18)
CAMERON, JOSEPH M., A345 Physics Bldg.,
Natl. Bureau of Standards, Washington, D.C.
20234 (F-1)
CAMPAGNONE, ALFRED F., P.E., 9321 Warfield
Rd., Gaithersburg, Md. 20760 (F)
CAMPBELL, LOWELL E., B.S., 10100 Riggs Rd.,
Adelphi, Md. 20783 (F-12, 13)
CANNON, E. W., Ph.D., 5 Vassar Cir., Glen Echo,
Md. 20768 (F-1, 6)
CANTELO, WILLIAM W., Ph.D., 11702 Wayneridge
St., Fulton, Md. 20759 (F-24, 6)
CARNS, HARRY R., Bg. 001, Agr. Res. Cent. (W.),
USDA, Beltsville, Md. 20705 (M-10, 33)
CARROLL, Miss KAREN E., 11565 N. Shore Dr.,
#21A, Reston, Va. 22090 (M)
CARROLL, WILLIAM R., 4802 Broad Brook Dr.,
Bethesda, Md. 20014 (F)
CARTER, HUGH, 2039 New Hampshire Ave.,
N.W., Washington, D.C. 20009 (F)
CASH, EDITH K., 505 Clubhouse Rd., Bingham-
ton, N.Y. 13903 (E-10)
CASSEL, JAMES M., Ph.D., 12205 Sunnyview Dr.,
Germantown, Md. 20767 (F-4, 21)
CHANEY, JAMES G., Rt. 2, Box 232L, Sotterley
Hghts., Hollywood, Md. 20636 (M)
CHAPLIN, HARVEY P., Jr., 1561 Forest Villa
Lane, McLean, Va. 22101 (F-22)
CHAPLINE, W. R., 4225. 43nd. ‘St.,
Washington, D.C. 20016 (E-6, 10, 11)
CHERTOK, BENSON T., Ph.D., Dept. of Physics,
American Univ., Wash. D.C. 20016 (M)
CHEZEM, CURTIS G., Ph.D., Middle South Serv.
Inc., P.O. Box 61000, New Orleans, La. 70161
(F)
CHI, MICHAEL, Sc.D., Civil-Mech. Engr. Dept.,
Catholic Univ., Washington, D.C. 20064
(F-6, 14)
CHOPER, JORDAN J., 121 Northway, Greenbelt,
Md. 20770 (M)
CHRISTIAN, ERMINE A., 7802 Lakecrest Dr.,
Greenbelt, Md. 20770 (M-1, 25)
CHRISTIANSEN, MERYL N., Ph.D., Chief Plant
Stress Lab. USDA ARS, Beltsville, Md.
20705 (F-6, 33)
CHURCH, LLOYD E., D. D. S., Ph.D., 8218 Wis-
consin Ave., Bethesda, Md. 20014 (F-1, 9, 19,
21)
CLAIRE, CHARLES N., 4403 14th St., N.W.,
Washington, D.C. 20011 (F-1, 12)
CLARK, FRANCIS E., ARS Research Lab., P.O.
Box E, Ft. Collins, Colo. 80521 (F)
N.W.,
174
CLARK, GEORGE E., Jr., 4022 North Stafford
St., Arlington, Va. 22207 (F)
CLARK, JOAN ROBINSON, Ph.D., U.S. Geologi-
cal Survey, 345 Middlefield Rd., Menlo Park,
Calif. 94025 (F-7)
CLAUSEN, CURTIS P., 2541 Northwest 58th,
Oklahoma City, Okla. 73113 (E-5)
CLEEK, GIVEN W., 5512N. 24th St., Arlington, Va.
22205 (M-4, 28, 32)
CLEMENT, J. REID, Jr., 3410 Weltham St.,
Suitland, Md. 20023 (F)
CLEVEN, GALE W., Ph.D., RD. 4, Box 334B,
Lewistown, Pa. 17044 (F-1)
COATES, JOSEPH F., Off. of Tech Assessment
U.S. Congress Wash. D.C. 20510 (F)
COHN, ROBERT, M.D., 7221 Pyle Road, Be-
thesda, Md. 20034 (F-1)
COLE, KENNETH S., Ph.D., National Institutes
of Health, Bethesda, Md. 20014 (F-1)
COLE, RALPH I|., 3431 Blair Rd., Falls Church,
Va. 22041 (F-13)
COLLINS, HENRY B., Dept. Anthropology,
Smithsonian Inst., Washington, D.C. 20560
(E-2)
COLWELL, R. R., Ph.D., Dept. of Microbiology,
Univ. of Maryland, College Park, Md. 20742
(F-6, 16)
COMPTON, W. DALE, Sci. Res. Staff, Ford
Motor Co., P.O. Box 1603, Dearborn,
Mich. 48121 (F)
CONGER, PAUL S., M.S., U.S. National Museum,
Washington, D.C. 20560 (E)
CONNORS, PHILIP I., 12909 Two Farm Dr.,
Silver Spring, Md. 20904 (F)
COOK, HAROLD T., Ph.D., 1513 Londontown Ct.,
Edgewater, Md. 21037 (E-10)
COOK, RICHARD K., Ph.D., 8517 Milford Ave.
Silver Spring, Md. 20910 (F-1, 25)
COONS, GEORGE H., Ph.D., 7415 Oak Lane,
Chevy Chase, Md., 20015 (E-10)
COOPER, KENNETH W., Ph.D. Dept. Biol., Univ.
of California, Riverside, Cal. 92502 (F-5)
CORLIS, EDITH L. R., Mrs., 2955 Albemarle
St. N.W., Washington, D.C. 20008 (F)
CORLISS, JOHN O., Ph.D., 9512 E. Stanhope
Rd., Kensington, Md. 20795 (F)
CORLISS, JOSEPH J., 6618 Bellview Dr., Colum-
bia, Md. 21046 (M)
CORNFIELD, JEROME, G.W.V. Biostat-Ctr., 7979
Old Georgetown Rd., Bethesda, Md. 20014
F)
Sec LOUIS, Chief 241. 02, Natl. Bureau
of Standards, Washington, D.C. 20234 (F)
COTTERILL, CARL H., M.S., U.S. Bureau of Mines
2401, E. St., N.W., Washington, D.C. 20241
(F-36)
COX, EDWIN L., NAL, Room 013, Beltsville,
Md. 20705 (F-6)
COYLE, THOMAS D., National Bureau of Stand-
ards, Washington, D.C. 20234 (F-4, 6)
CRAFTON, PAUL A., P.O. Box 454, Rockville,
Md. 20850 (F)
CRAGOE, CARL S., 6206 Singleton Place,
Bethesda, Md. 20034 (E-1)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
CRANE, LANGDON T., Jr., 7103 Oakridge Ave.,
Chevy Chase, Md. 20015 (F-1, 6)
CREITZ, E. CARROLL, 10145 Cedar Lane, Ken-
sington, Md. 20795 (E-32)
CROSSETTE, GEORGE, 4217 Glenrose St., Ken-
sington, Md. 20795 (M-6, 17)
CULBERT, DOROTHY K., 812 A St., S.E., Wash-
ington, D.C. 20003 (M-6)
CULLINAN, FRANK P., 4402 Beechwood Rad.,
Hyattsville, Md. 20782 (E-6, 10, 33)
CULVER, WILLIAM H., Ph.D., 2841 Chesapeake
St., N.W., Washington, D.C. 20008 (M)
CURRAN, HAROLD R., Ph.D., 3431 N. Randolph
St., Arlington, Va. 22207 (E-6, 16)
CURRIE, CHARLES L., S.J., President, Wheeling
College, Wheeling, W.Va. 26003 (F-4)
CURTIS, ROGER, W., Ph.D., 6308 Valley Rd.,
Bethesda, Md. 20034 (F)
CURTISS, LEON F., 1690 Bayshore Drive, Eng-
lewood, Fla. 33533 (E-1)
CUTHILL, JOHN R., Ph.D., 12700 River Rad.,
Potomac, Md. 20854 (F-20, 36)
CUTKOSKY, ROBERT D., 19150 Roman Way,
Gaithersburg, Md. 20760 (F)
D
DARRACOTT, HALVOR T., M.S., 3325 Mansfield
Rd., Falls Church, Va. 22041 (F-13, 34, 38)
DAVIS, CHARLES M., Jr., Ph.D., 8458 Portland
Pl., McLean, Va. 22101
DAVIS, R. F., Ph.D., Chairman, Dept. of Dairy
Science, Univ. of Maryland, College Park,
Md. 20742 (F)
DAVISSON, JAMES W., Ph.D., 400 Cedar Ridge
Dr., Oxon Hill, Md. 20021 (F-1)
DAWSON, ROY C., 7002 Chansory Lane, Hyatts-
ville, Md. 20782 (E-16)
DAWSON, VICTOR C. D., 9406 Curran Rd., Silver
Spring, Md. 20901 (F)
DE BERRY, MARIAN B., 3608 17th St., N.E.,
Washington, D.C. 20018 (M)
BEDRICK, R. L., Bg. 13, Rm. 3W13, NIH,
Bethesda, Md. 20014 (F-1)
DEITZ, VICTOR R., Ph.D., 3310 Winnett Rd.,
Chevy Chase, Md. 20015 (F)
DE PUE, LELAND A., Ph.D., 9710 Dilston St.,
Silver Spring, Md. 20903 (F-6, 20)
DE VOE, JAMES R., 17708 Parkridge Dr., Gai-
thersburg, Md. 20760 (F-4, 6)
DE WIT, ROLAND, Metallurgy Division, Natl.
Bureau of Standards, Washington, D.C.
20234 (F-1, 6, 36)
DELANEY, WAYNE R., The Wyoming Apts., 111,
2022 Columbia Rd., N.W., Washington, D.C.
20009 (M-6, 20, 22, 32)
DEMUTH, HAL P., MSEE, 4025 Pinebrook Rad.,
Alexandria, Va. 22310 (F-13, 17)
DENNIS, BERNARD K., 915 Country Club Dr.,
Vienna, Va. 22180 (F)
DERMEN, HAIG, Ph.D., Plant Industry Station,
Beltsville, Md. 21250 (F)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
DESLATTES, RICHARD D., Jr., 610 Aster Blvd.,
Rockville, Md. 20850 (F)
DETWILER, SAMUEL B., Jr., 631 S. Walter Reed
Dr., Arlington, Va. 22204 (F-4, 39)
DEVIN, CHARLES, 629 Blossom Dr., Rockville,
Md. 20850 (M)
DI MARZIO, E. A., 14205 Parkvale Rd., Rockville,
Md. 20853 (F)
DIAMOND, J. J., Physics B-150, Natl. Bureau of
Standards, Washington, D.C. 20234 (F-1, 4,
6, 28)
DIAMOND, PAULINE, Ph.D., 6436 Bannockburn
Dr., Bethesda, Md. 20034
DICKSON, GEORGE, M.A., Dental and Med.
Materials Sect., National Bureau of Stand-
ards, Washington, D.C. 20234 (F-6, 21)
DIEHL, WALTER S., 4501 Lowell St., N.W.,
Washington, D.C. 20016 (E-22)
DIEHL, WILLIAM W., Ph.D., 4435 N. Pershing Dr.
Arlington, Va. 22203 (E-3, 10)
DIGGES, THOMAS G., 3900 N. Albemarie St.,
Arlington, Va. 22207 (E-20)
DIMOCK, DAVID A., 4800 Barwyn House Rad.,
#114, College Park, Md. 20740 (M-13)
DIXON, PEGGY A., Ph.D., 422 Hillsboro Dr., Silver
Spring, Md. 20902 (F)
DOCTOR NORMAN, B.S., 3814 Littleton St.,
Wheaton, Md. 20906 (F-13)
DOFT, FLOYD S., Ph.D., 6416 Garnett Drive, Ken-
wood, Chevy Chase, Md. 20015 (E-4, 6, 19)
DONNERT, HERMANN J., Ph.D., RFD 4, Box 136,
Terra Heights, Manhattan Ks. 66502 (F)
DONOVICK, RICHARD, Ph.D., 16405 Alden Ave.,
Gaithersburg, Md. 20760 (F-4, 6, 16, 19)
DOUGLAS, CHARLES A., Sec. 221.12, Natl.
Bureau of Standards, Washington, D.C.
20234 (F-1, 6, 32)
DOUGLAS, THOMAS B., Ph.D., 3031 Sedgwick
St., N.W., Washington, D.C. 20008 (F-4)
DRAEGER, R. HAROLD, M.D., 1201 N. 4th Ave.,
Tucson, Ariz. 85705 (E-32)
DRECHSLER, CHARLES, Ph.D., 6915 Oakridge
Rd., University Park (Hyattsville), Md. 20782
(E-6, 10)
DUBEY, SATYA D., Ph.D., 7712 Groton Rd.,
Bethesda, Md. 20034 (F)
DUERKSEN, J. A., 3134 Monroe St., N.E. Wash-
ington, D.C. 20018 (E-1, 6)
DUFFEY, DICK, Ph.D., Nuclear Engineering,
Univ. Maryland, College Park, Md. 20742 (F-1,
26)
DUNCOMBE, RAYNOR L., Ph.D., 1804 Vance
Circle, Austin, Tx. 78701 (F-1, 22)
DUNKUM, WILLIAM W., M.S., 3503 Old Dominion
Blvd., Alexandria, Va. 22305 (F-31)
DUNN, JOSEPH P., 14721 Flintstone La., Silver
Spring, Md. 20904 (M)
DUNNING, K. L., Ph.D., Code 6603D, Naval Res.
Lab., Washington, D.C. 20390 (F-1)
DU PONT, JOHN ELEUTHERE, P.O. Box 358,
Newtown Square, Pa. 19073 (M)
DUPRE, ELSIE, Mrs., Code 5536A, Optical Sci.
Div., Naval Res. Lab., Washington, D.C. 20390
(F-32)
175
DURIE, EDYTHE G., 5011 Larno Dr., Alexandria,
Va. 22310 (F)
DURRANI, S. H., Ph.D., 17513 Lafayette Dr.,
Olney, Md. 20832 (F)
DURST, RICHARD A., Ph.D., Chemistry Bldg. Rm.
A 221, Natl. Bur. of Standards, Washington,
D.C. 20234 (F-4, 6)
DYKE, E. D., 173 Northdown Rd., Margate, Kent,
England (M)
E
EASTER, DONALD, Inst. Gas Technology, 1825
K St., N.W., Washington, D.C. 20006 (M)
EDDY, BERNICE E., Ph.D., 6722 Selkirk Ct.,
Bethesda, Md. 20034 (E)
EDMUNDS, LAFE R., Ph.D., 6003 Leewood Dr.,
Alexandria, Va. 22310 (F-5)
EGOLF, DONALD R., 3600 Cambridge Court,
Upper Marlboro, Md. 20870 (F-10)
EISELE, JOHN A., 3310 Curtis Dr., #202, Hillcrest
Hghts., Md. 20023 (F)
EISENBERG, PHILLIP, C.E., 6402 Tulsa Lane,
Bethesda, Md. 20034 (M-14, 22, 25)
EISENHART, CHURCHILL, Ph.D., Met B-268,
National Bureau of Standards, Washington,
D.C. 20234 (F-1, 30, 38)
EL-BISI, HAMED M., Ph.D., 135 Forest Rd., Millis,
Ma. 02054 (M-16)
ELLINGER, GEORGE A., 739 Kelly Dr., York, Pa.
17404 (E-6)
ELLIOT, F. E., 7507 Grange Hall Dr., Oxon Hill,
Md. 20022 (E)
EMERSON, K. C., Ph.D., 2704 Kensington St.,
Arlington, Va. 22207 (F)
EMERSON, W. B., 415 Aspen St., N.W., Wash-
ington, D.C. 20012 (E)
ENNIS, W. B., Jr., Ph.D., Agricultural Res. Ctr.
U. of Florida, 3205 S.W. 70th Ave., Ft. Lauder-
dale, Fl. 33314 (F-6)
ETZEL, HOWARD W., Ph.D., 7304 River Hill Rd.,
Oxon Hill, Md. 20021 (F-6)
EWERS, JOHN C., 4432 26th Rd., N, Arlington,
Va. 22207 (F-2)
F
FAHEY, JOSEPH J., U.S. Geological Survey,
Washington, D.C. 20242 (E-4, 6, 7)
FALLON, ROBERT, 8251 Toll House Rd., Annan-
dale, Va. 22003 (F)
FAN, SHOU SHAN, 2313 Glenallen Ave., Apt. 202,
Silver Spring, Md. 20906 (F-18)
FARROW, RICHARD P., National Canners Assn.,
1950 6th St., Berkeley, Calif. 94710 (F-4, 6, 27)
FATTAH, JERRY, 3451 S. Wakefield St., Arling-
ton, Va. 22206 (M-4, 39)
176
FAULKNER, JOSEPH A., 1007 Sligo Creek Pky.,
Takoma Park, Md. 20012 (F-6)
FAUST, GEORGE T., Ph.D., 9907 Capitol View
Ave., Silver Spring, Md. 20910 (F-7, 31)
FAUST, WILLIAM R., Ph.D., 5907 Walnut St.,
Temple Hills, Md. 20031 (F-1, 6)
FAYER, RONALD, Ph.D., USDA ARS Animal Para-
sitology |, Beltsville, Md. 20705 (M-15)
FEARN, JAMES E., Ph.D., Materials and Com-
posites Sect., Natl. Bureau of Standards,
Washington, D.C. 20234 (F-4)
FELDMAN, SAMUEL, NKF Engr. Associates,
Inc., 8720 Georgia Ave., Silver Spring, Md.
20910 (M-25)
FELSHER, MURRAY, Ph.D., NASA Cocle Ek.,
Wash. D.C. 20546 (M-1, 7)
FERRELL, RICHARD A., Ph.D., Dept. of Physics,
University of Maryland, College Park, Md.
20742 (F-6, 31)
FIFE, EARL H., Jr., Box 122, Royal Oak, Md.
21662 (E)
FILIPESCU, NICOLAE, M.D., Ph.D., 4836 S. 7th
St., Arlington, Va. 22204 (F)
FINN, EDWARD J., 4211 Oakridge La., Chevy
Chase, Md. 20015 (F-1, 31)
FLETCHER, DONALD G., Natl. Bureau of Stand-
ards, Rm. A102, Bldg. 231-IND, Washington,
D.C. 20234 (M-4)
FLICK, DONALD F., 930 19th St. So., Arlington,
Va. 22202 (F-19)
FLINN, DAVID R., 8104 Bernard Dr., Oxon Hill,
Md. 20022 (F)
FLORIN, ROLAND E., Ph.D., Polymer Stab. and
React. Sect., B-324, National Bureau of
Standards, Washington, D.C. 20234 (F-4, 6)
FLYNN, DANIEL R., 17500 Ira Court, Derwood,
Md. 20855 (F)
FLYNN, JOSEPH H., Ph.D., 5309 Iroquois Rd.,
Bethesda, Md. 20016 (F-4)
FONER, S. N., Applied Physics Lab., The Johns
Hopkins University, 11100 Johns Hopkins
Rd., Laurel, Md. 20810 (F-1)
FOOTE, RICHARD H., Sc.D., 8807 Victoria Road,
Springfield, Va. 22151 (F-5, 6)
FORSYTHE, ALLAN L., Boher Bridge Rd., RFD. 3,
Lincoln, Ma. 01773 (F)
FORZIATI, ALPHONSE F., Ph.D., 9812 Dameron
Dr., Silver Spring, Md. 20902 (F-1, 4, 29)
FORZIATI, FLORENCE H., Ph.D., 9812 Dameron
Dr., Silver Spring, Md. 20902 (F-4)
FOSTER, AUREL O., 4613 Drexel Rd., College
Park, Md. 20740 (E-15, 24)
FOURNIER, ROBERT O., 108 Paloma Rad., Por-
tola Valley, Calif. 94025 (F-6, 7)
FOWELLS, H. A., Ph.D., 10217 Green Forest,
Silver Spring, Md. 20903 (E-11)
FOWLER, EUGENE, Int. Atomic Energy Agency,
Kartner Ring 11, A-1011, Vienna, Austria
(M-26)
FOWLER, WALTER B., M.A., Code 673, Goddard
Space Flight Center, Greenbelt, Md. 20771
(M-32)
FOX, DAVID W., The Johns Hopkins Univ.,
Applied Physics Lab., Laurel, Md. 20810 (F)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
FOX, WILLIAM B., 1813 Edgehill Dr., Alexandria,
Va. 22307 (F-4)
FRANKLIN, PHILIP J., 5907 Massachusetts Ave.
Extended, Washington, D.C. 20016 (F-4, 13,
39)
FRANZ, GERALD J., M.S., Box 695, Bayview,
Id. 83803 (F-6, 25)
FREEMAN, ANDREW F., 5012 N. 33rd. St., Arling-
ton, Va. 22207 (M)
FREDERIKSE, H. P. R., Ph.D., 9625 Dewmar
Lane, Kensington, Md. 20795 (F)
FRENKIEL, FRANCOIS N., Applied Math. Lab.,
Naval Ship Res. & Develop. Ctr., Bethesda,
Md. 20034 (F-1, 22, 23)
FRIEDMAN, MOSHE, 3850 Tunlaw Rd., Washing-
ton, D.C. 20007 (F)
FRIESS, S. L., Ph.D., Environmental Biosciences
Dept., Naval Med. Res. Inst. NNMC, Bethesda,
Md. 20014 (F-4, 39)
FRUSH, HARRIET L., 4912 New Hampshire Ave.,
N.W., Apt. 104, Washington, D.C. 20011
(F-4, 6)
FULLMER, IRVIN H., Lakeview Terrace Retire-
ment Center, P.O. Box 116, Altoona, Fla.
32702 (E-1, 6, 14)
FULTON, ROBERT A., 530 Merrie Dr., Corvallis,
Oregon 97330 (E-1, 4, 6)
FURUKAWA, GEORGE T., Ph.D. National Bureau
of Standards, Washington, D.C. 20234 (F-1,
4, 6)
FUSILLO, MATTHEW H., VA Hospital, 50 Irving
St., N.W. Wash. D.C. 20422 (M)
G
GAFAFER, WILLIAM M., 133 Cunningham Dr.,
New Smyrna Beach, Fla. 32069 (E)
GAGE, WILLIAM, Ph.D., 2146 Florida Ave., N.W.,
Washington, D.C. 20008 (F-2)
GALLER, SIDNEY, 6242 Woodcrest Ave., Balti-
more, Md. 21209 (F-6)
GALTSOFF, PAUL S., Ph.D., Morgan Rad.,
Woods Hole, Mass. 20543 (E-3)
GALVIN, CYRIL J., Jr., 7728 Brandeis Way,
Springfield, Va. 22153 (F-7, 18, 30)
GANT, JAMES O., Jr., M.D., 4349 Klingle St., N.W.
Wash. D.C. 20016 (M)
GARNER, C. L., The Garfield, 5410 Connecticut
Ave., N.W., Washington, D.C. 20015 (E-1, 4,
i272 18)
GARVIN, DAVID, Ph.D., 18700 Walker's Choice
Rd., Apt. 519, Gaithersburg, Md. 20760 (F-4)
GAUM, CARL H., 9609 Carriage Rd., Kensington,
Md. 20795 (F-18)
GUANAURD, GUILLERMO C., Ph.D., 4807 Macon
Rd., Rockville, Md. 20852 (M-6, 14, 25)
GHAFFARI, ABOLGHASSEN, Ph.D., D.Sc., 7109
Connecticut Ave., N.W., Washington, D.C.
20015 (L-1, 38)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
GHOSE, RABINDRA N., 8167 Mulholland Terr.,
Los Angeles Hill, Calif. 90046 (F)
GIACCHETTI, ATHOS, Dept. Sci. Affairs, OAS,
1735 Eye St., N.W., Washington, D.C. 20006
(M-32)
GIBSON, JOHN E., Box 96, Gibson, N.C. 28343
(E)
GIBSON, KASSON S., 4817 Cumberland St.,
Chevy Chase, Md. 20015 (E)
GINTHER, ROBERT J., Code 6445, U.S. Naval
Res. Lab., Washington, D.C. 20390 (F-28, 29)
GISH, OLIVER H., 7107 S. Indian River Dr., Fort
Pierce, Fla. 33450 (E-1, 23)
GIWER, MATTHIAS M., 204-206 S. St. Asaph St.,
Alexandria, Va. 22314 (M)
GLADSTONE, VIC S., 8200 Andes Ct., Baltimore,
Md. 21208 (M-6, 25)
GLASGOW, A. R., Jr., Ph.D., 4116 Hamilton St.,
Hyattsville, Md. 20781 (F-4, 6)
GLICKSMAN, MARTIN E., 8 Via Maria Scotia, N.Y.
12302 (F-20, 36)
GLUCKSTERN, ROBERT L., Ph.D., Chancellor
Univ. of Md., College Park, Md. 20742 (F)
GODFREY, THEODORE B., 7508 Old Chester
Rd., Bethesda, Md. 20034 (E)
GOFF, JAMES F., Ph.D., 3405 34th Pl., N.W.,
Washington, D.C. 20016 (F-1)
GOLDBERG, MICHAEL, 5823 Potomac Ave.,
N.W., Washington, D.C. 20016 (F-1, 38)
GOLDBERG, ROBERT N., Ph.D., 19610 Brassie
Pl., Gaithersburg, Md. 20760 (F)
GOLDMAN, ALAN J., Ph.D., Applied Math. Div.
Inst. for Basic Standards, Natl. Bureau of
Standards, Washington, D.C. 20234 (F-34, 38)
GOLDSMITH, HERBERT, 238 Congressional
Lane, Rockville, Md. 20852 (M)
GOLUMBIC, CALVIN, 6000 Highboro Dr.,
Bethesda, Md. 20034 (F)
GONET, FRANK, 4007 N. Woodstock St., Arling-
ton, Va. 22207 (F-4)
GOODE, ROBERT J., B.S., Strength of Metals
Br., Code 6380, Metallurgy Div., U.S.N.R.L.,
Washington, D.C 20390 (F-6, 20)
GORDON, CHARLES L., 5512 Charles St.,
Bethesda, Md. 20014 (E-1, 4, 6)
GORDON RUTH E., Ph.D., Waksman Inst. of
Microbiology, Rutgers Univer., New Bruns-
wick, N.J. 08903 (F-16)
GRAHN, Mrs. ANN, M.A., 849 So. La Grange Rd.,
La Grange, Ill. 60525 (M)
GRAMANN, RICHARD H., 1613 Rosemont CT,
McLean, Va. 22101 (M)
GRAY, ALFRED, Dept. Math., Univ. of Maryland,
College Park, Md. 20742 (F)
GRAY, IRVING, Ph.D., Georgetown Univ., Wash-
ington, D.C. 20007 (F-19)
GREENOUGH, M. L., M.S., Greenough Data
Assoc., 616 Aster Blvd., Rockville, Md. 20850
(F)
GREENSPAN, MARTIN, 12 Granville Dr., Silver
Spring, Md. 20902 (F-1, 25)
GRISAMORE, NELSON T., Nat. Acad. Sci., 2101
Constitution Ave., N.W., Washington, D.C.
20418 (F)
177
GRISCOM, DAVID L., Ph.D., Material Sci. Div.,
Naval Res. Lab., Washington, D.C. 20375
(F-6, 28)
GROSSLING, BERNARDO F., Rm. 7213, USGS
Nat. Ctr., 12201 Sunrise Valley Dr., Reston,
Va. 22092 (F)
GURNEY, ASHLEY B., Ph.D., Systematic Ento-
mology Laboratory, USDA, % U.S. National
Museum, NHB-105, Washington, D.C. 20560
(F-3, 5, 6)
GUTTMAN, CHARLES M., 9510 Fern Hollow Way
Gaithersburg, Md. 20760 (F)
[-f
HAAR, JAMES W., 9503 Nordic Dr., Lanham,
Md. 20801 (M)
HACSKAYLO, EDWARD, Ph.D., Agr. Res. Ctr.,
West, Beltsville, Md. 20705 (F-7, 10, 11, 33)
HAENNI, EDWARD O., Ph.D., 7907 Glenbrook
Rd., Bethesda, Md. 20014 (F-4, 39)
HAGAN, LUCY B., Ph.D., Natl. Bur. Stds., Rm.
A155, Bg. 221, Washington, D.C. 20234 (M-4,
32)
HAINES, KENNETH A., M.S., ARS, USDA, Federal
Center Bldg., Hyattsville, Md. 20781 (F-5, 24)
HAKALA, REINO W., Ph.D., 707 Prospect St.,
Sault Ste. Marie, Mi. 49783 (F)
HALL, E. RAYMOND, Museum of Natural History,
Univ. of Kansas, Lawrence, Kans. 66044 (E-3,
6)
HALL, R. CLIFFORD, M.F., 316 Mansion Drive,
Alexandria, Va. 22302 (E-11)
HALL, STANLEY A., 9109 No. Branch Dr.,
Bethesda, Md. 20034 (F-24)
HALL, WAYNE C., Ph.D., 557 Lindley Dr.,
Lawrence, Kans. 66044 (E-6, 13)
HALLER, WOLFGANG, Ph.D., National Bureau
of Standards, Washington, D.C. 20234 (F)
HAMBLETON, EDSON J., 5140 Worthington Dr.,
Washington, D.C. 20016 (E-3, 5, 6)
HAMER, WALTER J., Ph.D., 3028 Dogwood St.,
N.W., Washington, D.C. 20015 (F-6, 13, 29)
HAMMER, GUYS, Il, 4626 River Rd., Chevy Chase,
Md. 20015 (M-12, 13)
HAMMERSCHMIDT, W. W., Ph.D., 7818 Holmes
Run Dr., Falls Church, Va. 22042 (M)
HAMMOND, DAVID H., 14 Chappel St., Brock-
port, N.Y. 14420 (M-10)
HAMPP, EDWARD G., D.D.S., National Institutes
of Health, Bethesda, Md. 20014 (F-21)
HANCOCK, JUDITH M., Biol. Dept., St. Joseph’s
College, North Windham, Me. 04062 (F)
HAND, CADET H., Jr., Bodega Marine Lab.,
Bodega Bay, Calif. 94923 (F-6)
HANSEN, LOUIS S., D.D.S., School of Dentistry,
San Francisco, Med. Center, Univ. of Calif.,
San Francisco, Calif. 94122 (F-21)
HANSEN, MORRIS, H., M.A., Westat Research,
Inc., 11600 Nebel St., Rockville, Md. 20852
(F)
178
HARDENBURG, ROBERT E., Ph.D., Agr. Mktg.
Inst., Agr. Res. Ctr (W), Beltsville, Md. 20705
(F-6) 7
HARRINGTON, FRANCIS D., Ph.D., 4600 Ocean
Beach Blvd., #204, Cocoa Beach, Fla.
32931 (F)
HARRINGTON, M. C., Ph.D., 4545 Connecticut
Ave., N.W., Apt. 334, Washington, D.C. 20008
(E-1, 22, 32)
HARRIS, MILTON, Ph.D., 3300 Whitehaven St.,
N.W., Suite 500, Washington, D.C. 20007 (F)
HARRISON, W. N., 3734 Windom PI., N.W.,
Washington, D.C. 20008 (F)
HARTLEY, JANET W., Ph.D., National Inst. of
Allergy & Infectious Diseases, National In-
stitutes of Health, Bethesda, Md. 20014 (F)
HARTMANN, GREGORY K., 10701 Keswick St.,
Garrett Park, Md. 20766 (F-1, 25)
HARTZLER, MARY P., 3326 Hartwell Ct., Falls
Church, Va. 22042 (M-6)
HASKINS, C. P., Ph.D., 2100 M St., N.W., Suite
600 Washington, D.C. 20037 (F)
HASS, GEORG H., 7728 Lee Avenue, Alexandria,
Va. 22308 (F-32)
HAUPTMAN, HERBERT Ph.D., Med. Fndn. of
Buffalo, 73 High St., Buffalo, N.Y. 14203
(F-1, 6, 38)
HAYDEN, GEORGE A., 1312 Juniper St. N.W.,
Washington, D.C. 20012 (M)
HAYES, PATRICK, Ph.D., 5565 Columbia Pike,
#812, Arlington, Va. 22204 (F-38)
HEADLEY, ANNE R., Ph.D., Ms., 2500 Virginia
Ave., N.W., Washington, D.C. 20037 (F)
HEANEY, JAMES B., 6 Olivewood Ct., Greenbelt,
Md. 20770 (F)
HEIFFER, M. H., Whitehall, #701, 4977 Battery
La., Bethesda, Md. 20014 (F)
HEINRICH, KURT F., 804 Blossom Dr., Woodley
Gardens, Rockville, Md. 20850 (F)
HENDERSON, E. P., Div. of Meteorites, U.S. Na-
tional Museum, Washington, D.C. 20560 (E-7)
HENDRICKSON, WAYNE A., M.D., Ph.D., Lab. for
the Structure of Matter, Naval Res. Lab. Code
6030, Washington, D.C. 20375 (F)
HENNEBERRY, THOMAS J., 1409 E. North
Share, Temple, Ariz. 85282 (F)
HENVIS, BERTHA W., Code 5277, Naval Res.
Lab., Washington, D.C. 20375 (M)
HERBERMAN, RONALD B., 8528 Atwell Rd.,
Potomac, Md. 20854 (F)
HERMACH, FRANCIS L., 2415 Eccleston St.,
Silver Spring, Md. 20902 (F-1, 6, 13, 25)
HERMAN, ROBERT, Ph.D., Traffic Sci. Dept.,
General Motors Res. Lab., 12 Mi & Mound
Rds., Warren, Mich. 48090 (F)
HERSCHMAN, HARRY K., 4701 Willard Ave.,
Chevy Chase, Md. 20015 (E)
HERSEY, JOHN B., 923 Harriman St., Great Falls,
Va. 22066 (M-25)
HERSEY, MAYO D., M.A., Div. of Engineering,
Brown Univ., Providence, R.|. 02912 (E-1)
HERZFELD, KARL F., Dept. of Physics, Catholic
Univ., Washington, D.C. 20017 (E-1)
HESS, WALTER, C., 3607 Chesapeake St., N.W.,
Washington, D.C. 20008 (E-4, 6, 19, 21)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
HEWSTON, ELIZABETH, Felicity Cove, Shady
Side, Md. 20867 (F)
HEYDEN, FR. FRANCIS, Ph.D., Manila Observa-
tory, P.O. Box 1231, Manila, Philippines D-404
(E-32)
HIATT, CASPAR W., Ph.D., Univ. of Texas Health
Science Center, 7703 Floyd Curl Dr., San
Antonio, Texas 78284 (F)
HICKLEY, THOMAS J., 626 Binnacle Dr., Naples,
Fla. 33940 (F-13)
HICKOX, GEORGE H., Ph.D., 9310 Allwood Ct.,
Alexandria, Va. 22309 (E-6, 14, 18)
HILDEBRAND, EARL M., 11092 Timberline Dr.,
Sun City, Ariz. 85351 (E)
HILL, FREEMAN K., 12408 Hall’s Shop Rad.,
Fulton, Md. 20759 (F-1, 6, 22)
HILLABRANT, WALTER, Ph.D., Dept. Psychol-
ogy, Howard Univ., Washington, D.C. 20059
(M-40)
HILSENRATH, JOSEPH, 9603 Brunett Ave., Silver
Spring, Md. 20901 (F-1, 38)
HILTON, JAMES L., Ph.D. Agr. Res. Ctr. (W),
USDA, ARS, Beltsville, Md. 20705 (F-33)
HOBBS, ROBERT B., 7715 Old Chester Rad.,
Bethesda, Md. 20034 (F-1, 4, 39)
HOERING, THOMAS C., Carnegie Inst. of Wash-
ington, Geophysical Lab., 2801 Upton St.,
N.W. Washington, D.C. 20008 (F-4, 7)
HOFFMANN, C. H., Ph.D., 6906 40th Ave., Univer-
sity Park, Hyattsville, Md. 20782 (E-5, 11, 24)
HOGE, HAROLD J., Ph.D., 5 Rice Spring Lane,
Wayland, Me. 01778 (F-1)
HOLLIES, NORMAN R. S., Gillette Research
Institute, 1413 Research Blvd., Rockville, Md.
20850 (F-4)
HOLMGREN, HARRY D., Ph.D., P.O. Box 391,
College Park, Md. 20740 (F-1)
HOLSHOUSER, WILLIAM L., 513 N. Oxford St.,
Arlington, Va. 22203 (F-6, 20)
HONIG, JOHN G., Office, Dep. Chief of Staff
for Res., Dev. and Acquis., Army, The Penta-
gon, Washington, D.C. 20310 (F-1, 4, 34)
HOOD, KENNETH J., 2000 Huntington Ave.,
#1118, Alexandria, Va. 22303 (M-6, 33)
HOOVER, JOHN I., 5313 Briley Place, Washing-
ton, D.C. 20016 (F-1)
HOPP, HENRY, Ph.D., 7604 Winterberry Place
Bethesda, Md. 20034 (F-11)
HOPPS, HOPE E., Mrs., 1762 Overlook Dr., Silver
Spring, Md. 20903 (F-16, 19)
HORNSTEIN, IRWIN, Ph.D., 5920 Bryn Mawr Rd.,
College Park, Md. 20740 (F-4, 27)
HOROWITZ, E., Asst. Deputy Director, Institute
for Materials Res., National Bureau of Stand-
ards, Washington, D.C. 20234 (F)
HORTON, BILLY M., 14250 Larchmere Blvd.,
Shaker Heights, Ohio 44120 (F-1, 6, 13)
HUANG, KUN-YEN, M.D., Ph.D., 1445 Laurel
Hill Rd., Vienna, Va. 22180 (F)
HUBBARD, DONALD, 4807 Chevy Chase Dr.,
Chevy Chase, Md. 20015 (F-4, 6, 32)
HUBERT, LESTER F., 4704 Mangum Rad., College
Park, Md. 20740 (F-23)
HUDSON, COLIN M., Ph.D., Chief Scientist, U.S.
Army Armament Command, Rock Island, Ill.
61201 (F-22)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
HUDSON, GEORGE E., Code 026, Naval Surface
Weapons Ctr., White Oak, Silver Spring, Md.
20910 (F-1)
HUDSON, RALPH P., Ph.D., National Bureau of
Standards, Washington, D.C. 20234 (F-1)
HUGH, RUDOLPH, Ph.D., George Washington
Univ. Sch. of Med., Dept. of Microbiology,
2300 Eye St. N.W., Washington, D.C. 20037
(F-16)
HUNT, W. HAWARD, 11712 Roby Ave., Beltsville,
Md. 20705 (M-6)
HUNTER, RICHARD S., 9529 Lee Highway,
Fairfax, Va. 22030 (F-6, 27, 32)
HUNTER, WILLIAM R., M.S., Code 7143, U.S.
Naval Research Lab., Washington, D.C. 20390
(F-1, 32)
HUNTOON, R. D., Ph.D., 7901 40th Ave. N.,
#122, St. Petersburg, Fla. 33709 (F-1, 13)
HURDLE, BURTON G., 6222 Berkeley Rd., Alex-
andria, Va. 22307 (F-25)
HURTT, WOODLAND, Ph.D., ARS-USDA, P.O.
Box 1209, Frederick, Md. 21701 (M-33)
HUTCHINS, LEE M., Ph.D., Cacao Ctr., Institute of
Agriculture, Turrialba, Costa Rica (E-6, 10, 11)
HUTTON, GEORGE L., 809 Avondale Dr., W.
Lafayette, Ind. 47906 (F)
INSLEY, HERBERT, Ph.D., 5219 Farrington Rd.,
Washington, D.C. 20016 (E-1, 7)
IRVING, GEORGE W., Jr., Ph.D. 4836 Langdrum
Lane, Chevy Chase, Md. 20015 (F-4, 27)
IRWIN, GEORGE R., Ph.D., 7306 Edmonston Rad.,
College Park, Md. 20740 (F-1)
ISBELL, H. S., 4704 Blagden Ave.,
Washington, D.C. 20011 (F-4)
ISENSTEIN, Robert S., Animal Parasitology Inst.
Barc-East, USDA, Beltsville, Md. 20705 (M)
N.W.,
J
JACKSON, H. H. T., Ph.D., 122 Pinecrest Rd.,
Durham, N.C. (E-3)
JACKSON, PATRICIA C., Ms., Rm. 207, Bg. 001,
Agr. Res. Ctr. (W), ARS, USDA, Beltsville,
Md. 20705 (M)
JACOBS, WOODROW C., Ph.D., 6309 Bradley
Blvd., Bethesda, Md. 20034 (F-23)
JACOBSON, MARTIN, U.S. Dept. of Agriculture,
Agr. Res. Center (E) Beltsville, Md. 20705
(F-4, 24)
JACOX, MARILYN E., Ph.D., National Bureau of
Standards, Washington, D.C. 20234 (F-4)
JAFFE, LOUIS S., M.A., 1001 Highland Dr.,
Silver Spring, Md. 20910 (F-4)
JAMES, MAURICE T., Ph.D., Dept. of Ento-
mology, Washington State University, Pull-
man, Washington 99163 (E-5)
179
JANI, LORRAINE L., P.O. Box 898, Lutz, FI.
33549 (M)
JAROSEWICH, EUGENE, NMNH, Smithsonian
Inst., Washington, D.C. 20560 (M-4)
JEN, C. K., Applied Physics Lab., 8621 Georgia
Ave., Silver Spring, Md. 20910 (E)
JENSON, ARTHUR S., Ph.D., Westinghouse
Defense & Electronic Systems Ctr., Box 1521,
Baltimore, Md. 21203 (F-13, 31, 32)
JESSUP, R. S., 7001 W. Greenvale Pkwy., Chevy
Chase, Md. 20015 (F-1, 6)
JOHANNESEN, ROLF B., Ph.D., National Bureau
of Standards, Washington, D.C. 20234 (F-4, 6)
JOHNSON, CHARLES, Ph.D., Inst. for Fluid Dy-
namics & App. Math. Univ. of Md., College
Park, Md. 20850 (F)
JOHNSON, DANIEL P., 9222 Columbia Blvd.,
Silver Spring, Md. 20910 (F-1)
JOHNSON, KEITH C., 4422 Davenport St., N.W.,
Washington, D.C. 20016 (F)
JOHNSON, PHILLIS T., Ph.D., Nat. Marine
Fisheries Serv., Oxford Lab., Oxford, Md.
21654 (F-5, 6)
JOHNSTON, FRANCIS E., Ph.D., 307 W. Mont-
gomery Ave., Rockville, Md. 20850 (E-1)
JONES, HENRY A., 1115 South 7th St., El Centro,
Calif. 92243 (E)
JONES, HOWARD S., 6200 Sligo Mill Rd., N.E.,
Washington, D.C. 20011 (F-6, 13)
JORDAN, GARY BLAKE, 1012 Olmo Ct., San
Jose; Calif. 95129 (M-6, 13)
JUDD, NEIL M., Georgian Towers, Apt. 120-C,
8715 First Ave., Silver Spring, Md. 20910 (E-2,
6)
K
KABLER, MILTON N., Ph.D., 3109 Cunningham
Dr., Alexandria, Va. 22309 (F)
KAISER, HANS E., 433 South West Dr., Silver
Spring, Md. 20901 (M-6)
KALLBOM, CLAES, Box 13017, 58320, Link-
oping, 13, Sweden (M)
KARLE, ISABELLA, Code 6030, U.S. Naval Res.
Lab., Washington, D.C. 20375 (F-4, 6)
KARLE, JEROME, Code 6030, U.S. Naval Re-
search Lab., Washington, D.C. 20375
(F-1, 4)
KARR, PHILIP R., 5507 Calle de Arboles, Tor-
rance, Calif. 90505 (F-13)
KARRER, ANNIE M. H., Ph.D., Port Republic,
Md. 20676 (E-6)
KAUFMAN, H. P., Box 1135, Apt. 461, Fedhaven,
Fla. 33854 (F-12)
KEARNEY, PHILIP C., Ph.D., 13021 Blairmore St.,
Beltsville, Md. 20705 (F-4)
KEGELES, GERSON, RFD 2, Stafford Springs,
Conn. 06076 (F)
KENNARD, RALPH B., Ph.D., 3017 Military Rd.,
N.W., Washington, D.C. 20015 (E-1, 6, 31, 32)
KESSLER, KARL G., Ph.D., Optical Physics Div.,
Natl. Bureau of Standards, Washington, D.C.
20234 (F-1, 6, 32)
180
KEULEGAN, GARBIS H., Ph.D., 215 Buena Vista
Dr., Vicksburg, Miss. 39180 (F-1, 6)
KLEBANOFF, PHILIP S., Aerodynamics Sect.,
National Bureau of Standards, Washington,
D.C. 20234 (F-1, 22)
KLINGSBERG, CYRUS, Springs, Apt. 322, 303
Gage Blvd., Richland, Wash. 99352 (F-26, 28)
KLUTE, CHARLES H., Ph.D., Apt. 118, 4545 Con-
necticut Ave., N.W., Washington, D.C. 20008
(F-1, 4)
KNAPP, DAVID C., 4695 Osage Dr., Boulder, Colo.
80303 (F)
KNOBLOCK, EDWARD C., 12002 Greenleaf Ave.,
Rockville, Md. 20854 (F-4, 19)
KNOWLTON, KATHRYN, Apt. 837, 2122 Massa-
chusetts Ave., N.W., Washington, D.C. 20008
(F-4, 19)
KNOX, ARTHUR S., M.A., M.Ed., 2006 Columbia
Rd., N.W., Washington, D.C. 20009 (M-6, 7)
KNUTSON, LLOYD V., Ph.D., Systematic Ento-
mology Lab., ARS, USDA, Bg. 003, ARC (W),
Beltsville, Md. 20705 (F-5)
KRUGER, JEROME, Ph.D., Rm B254, Materials
Bldg., Natl. Bur. of Standards, Washington,
D.C. 20234 (F-4, 29)
KRUL, WILLIAM R., 13814 Sloan St., Rockville,
Md. 20853 (F)
KURTZ, FLOYD E., 8005 Custer Rd., Bethesda,
Md. 20014 (E-4)
KUSHNER, LAWRENCE M., Ph.D., Commis-
sioner, Consumer Product Safety Commis-
sion, Washington, D.C. 20207 (F-36)
L
LABENZ, PAUL J., 9504 Kingsley Ave., Bethesda,
Md. 20014
LADO, ROBERT, Ph.D., Georgetown Univ., Wash-
ington, D.C. 20007 (F)
LAKI, KOLOMAN, Ph.D., Bldg. 4, Natl. Inst. of
Health, Bethesda, Md. 20014 (F)
LANDIS, PAUL E., 6304 Landon Lane, Bethesda,
Md. 20034 (F-6)
LANDSBERG, H. E., 5116 Yorkville Rd., Temple
Hills, Md. 20031 (F-1, 23)
LANG, MARTHA E. C., B.S., Connecticut Ave.,
N.W., Washington, D.C. 20008 (F-6, 7)
LANGFORD, GEORGE S., Ph.D., 4606 Hartwick
Rd., College Park, Md. 20740 (E-5, 24)
LAPHAM, EVAN G., 5340 Cortez Ct., Cape Coral,
Fla. 33904 (E)
LARMORE, LEWIS, Off. of Naval Res., 800 N.
Quincey St., Arlington, Va. 22217 (M)
LASHOF, THEODORE W., 10125 Ashburton
Lane, Bethesda, Md. 20034 (F)
LASTER, HOWARD J., Ph.D., Dept. of Physics
& Astron., Univ. of Maryland, College Park,
Md. 20742 (F-1, 31)
LAWSON, ROGER H., 4912 Ridge View Lane,
Bowie, Md. 20715 (F)
LE CLERG, ERWIN L., 14620 Deerhurst Terrace,
Silver Spring, Md. 20906 (E-10)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
LEE, RICHARD H., RD 2, Box 143E, Lewes Del.
19958 (E)
LEINER, ALAN L., 580 Arastradero Rd., #804,
Palo Alto, Calif. 94306 (F)
LEJINS, PETER P., Univ. of Maryland, Inst.
Crim. Justice and Criminology, College Park,
Md. 20742 (F-10)
LENTZ, PAUL LEWIS, 5 Orange Ct., Greenbelt,
Md. 20770 (F-6, 10)
LEVY, SAMUEL, 2279 Preisman Dr., Schenec-
tady, N.Y. 12309 (F)
LIDDEL, URNER, 2939 Van Ness St. N.W., Apt.
1135, Washington, D.C. 20008 (E-1)
LIEBLEIN, JULIUS, 1621 E. Jefferson St., Rock-
vile, Md. 20852 (F-34)
LIERS, HENRY S., Intertechnology Corp., Box
340, Warrenton, Va. 22186 (F)
LINDQUIST, ARTHUR W., Rte. 1, Bridgeport,
Kans. 67424 (E-6)
LINDSEY, IRVING, M.A., 202 E. Alexandria Ave.,
Alexandria, Va. 22301 (E)
LING, LEE, 1608 Belvoir Dr., Los Altos, Calif.
94022 (E)
LINK, CONRAD B., Dept. of Horticulture, Univ.
of Maryland, College Park, Md. 20742 (F-6,
10)
LINNENBOM, VICTOR J., Ph.D., Code 8300,
Naval Res. Lab., Washington, D.C. 20390
(F-4)
LIPKIN, LEWIS E., Bg. 36, Rm. 40-25, NIH,
Bethesda, Md. 20014 (M)
LIST, ROBERT J., 1123 Hammond Pkwy., Alex-
andria, Va. 22302 (F-23)
LITTLE, ELBERT L., Jr., Ph.D., U.S. Forest Serv-
ice, Washington, D.C. 20250 (F-10, 11)
LOCKARD, J. DAVID, Ph.D., Botany Dept., Univ.
of Maryland, College Park, Md. 20742 (M-33)
LOEBENSTEIN, WILLIAM V., Ph.D., 8501 Sun-
dale Dr., Silver Spring, Md. 20910 (F-4, 21)
LONG, B. J. B., Mrs., 416 Riverbend Rd., Oxon
Hill, Md. 20022 (M)
LORING, BLAKE M., Sc.D., Rt. 2, Laconia, N.H.
03246 (F-20, 36)
LOTT, GEORGE A., 1812 Queens Lane, Apt. 218,
Arlington, Va. 22201 (M-1, 37)
LUSTIG, ERNEST, Ph.D., GMBF, D3301 Stock-
heim/Braunschweig, Mascheroder Weg 1, W.
Germany (F-4)
LYNCH, Mrs. THOMAS J., 4960 Butterworth PI.,
N.W., Washington, D.C. 20016 (M)
LYONS, JOHN W., Rte. 4, Box 261, Mount Airy,
Md. 21771 (F-4)
MA, TE-HSIU, Dept. of Biological Science, West-
ern Illinois Univ. Macomb, Ill. 61455 (F-3)
MADDEN, ROBERT P., A251 Physics Bldg., Natl.
Bureau of Standards, Washington, D.C.
20234 (F-32)
MAENGWYN-DAVIES, G. D., Ph.D., 15205 Totten-
ham Terr., Silver Spring, Md. 20206 (F-19)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
MAGIN, GEORGE B., Jr., 7412 Ridgewood Ave.,
Chevy Chase, Md. 20015 (F-6, 7, 26)
MAHAN, A. |., Ph. D., 10 Millgrove Place, Ednor,
Md. 20904 (F-1, 32)
MAIENTHAL, MILLARD, 10116 Bevern Lane,
Potomac, Md. 20854 (F-4)
MALITSON, IRVING, Physics, A251, Nat. Bureau
Standards, Washington, D.C. 20234 (F)
MALONEY, CLIFFORD J., Div. Biol. Standards,
Nat. Insts. Health, Bethesda, Md. 20014 (F)
MANDEL, H. GEORGE, Ph.D., Dept. of Phar-
macology, George Washington Univ. Sch. of
Med., Washington, D.C. 20037 (F-1)
MANDEL, JOHN, Ph.D., A345 Chem. Bg., Natl.
Bur. of Standards, Washington, D.C. 20234
(Fa)
MANDERSCHEID, RONALD W., Ph.D., 202
Montgomery Ave., 1, Rockville, Md. 20854 (M)
MANGUS, JOHN D., 6019 Berwyn Rd., College
Park, Md. 20740 (F)
MANNING, JOHN R., Ph.D., Metallurgy Div.,
Natl. Bur. of Standards, Washington, D.C.
20234 (F-20)
MARCHELLO, JOSEPH M., Ph.D., 3624 Marl-
borough Way, College Park, Md. 20742 (F)
MARCUS, MARVIN, Ph.D., Dept. Math., Univ. of
California, Santa Barbara, Calif. 93106 (F-6)
MARGOSHES, MARVIN, Ph.D., 69 Midland Ave.,
Tarrytown, N.Y. 10591 (F)
MARTIN, BRUCE D., P.O. Box 234, Leonardtown,
Md. 20650 (F-7)
MARTIN, JOHN H., Ph.D., 124 N.W. 7th St., Apt.
303, Corvallis, Oregon 97330 (E-6)
MARTIN, ROBERT H., 2257 N. Nottingham St.,
Arlington, Va. 22205 (M-23)
MARTON, L., Ph.D., Editorial Office, 4515 Lin-
nean Ave., N.W., Washington, D.C. 20008 (E-
Up us)
MARVIN, ROBERT S., 11700 Stony Creek Rad.,
Potomac, Md. 20854 (F-1, 4, 6)
MARYOTT, ARTHUR A., Natl. Bur. of Standards,
Washington, D.C. 20234 (F-4, 6)
MASON, HENRY LEA, Sc.D., 7008 Meadow Lane,
Chevy Chase, Md. 20015 (F-1, 6, 14, 35)
MASSEY, JOE T., Ph.D., 10111 Parkwood Dr.,
Bethesda, Md. 20014 (F-1, 13)
MATLACK, MARION, Ph.D., 2700 N. 25th St.,
Arlington, Va. 22207 (E)
MAUSS, BESSE D., Rural Rt. 1, New Oxford, Pa.
17350 (F)
MAXWELL, LOUIS R., Ph.D., 3506 Leland St.,
Chevy Chase, Md. 20015 (F)
MAY, DONALD C., Jr., Ph.D., 5931 Oakdale Rd.,
McLean, Va. 22101 (F)
MAY, IRVING, M.S., U.S. Geological Survey,
National Ctr. 923, Reston, Va. 22092 (F-4, 6, 7)
MAYOR, JOHN R., Francis Scott Key Hall, Rm.
1120H, Univ. Maryland, College Park, Md.
20742 (F)
MC BRIDE, GORDON W., Ch.E.,3323 Stuyvesant
PI. N.W., Chevy Chase, D.C. 20015 (F)
MC CAMY, CALVIN S., 54 All Angels Hitl Rd.,
Wappingers Falls, N.Y. 12590 (F-32)
MC CULLOUGH, JAMES M., Ph.D., 6209 Apache
St., Springfield, Va. 22150 (M)
181
MC CULLOUGH, N. B., Ph.D., M.D., Dept. of
Microbiology & Public Health, Michigan State
Univ., East Lansing, Mich. 48823 (F-6, 8)
MC ELHINNEY, JOHN, Ph.D., 11601 Stephen Rad.,
Silver Spring, Md. 20904 (F-1)
MC GUNIGAL, THOMAS E., J.D., 13013 Ingleside
Dr., Beltsville, Md. 20705 (F-1, 13)
MC INTOSH, ALLEN, 4606 Clemson Rd., College
Park, Md. 20740 (E-6, 15)
MC KELVEY, VINCENT E., Ph.D., 6601 Broxburn
Dr., Bethesda, Md. 20034 (F-7)
MC KINNEY, HAROLD H., 1620 N. Edgewood St.,
Arlington, Va. 22201 (E-6, 10, 16, 33)
MC KENZIE, LAWSON W., 5311 West Pathway,
Washington, D.C. 20016 (F)
MC NESBY, JAMES R.., Chief, Off. Air and Water
Measurement, Natl. Bur. of Standards, Wash-
ington, D.C. 20234 (F)
MC NICHOLAS, JOHN V., Ph.D., 1107 Nelson St.,
Rockville, Md. 20850 (M)
MC PHEE, HUGH C., 3450 Toledo Terrace, Apt.
425, Hyattsville, Md. 20782 (E-6)
MC PHERSON, ARCHIBALD T., Ph.D., 4005
Cleveland St., Kensington, Md. 20795 (F-1,
4, 6, 27)
MC WRIGHT, CORNELIUS G., 7409 Estaban PI.,
Springfield, Va. 22151 (M)
MEADE, BUFORD K., 5516 Bradley Blvd., Alex-
andria, Va. 22311 (F-17)
MEARS, FLORENCE, M. Ph.D., 8004 Hampden
Lane, Bethesda, Md. 20014 (F)
MEARS, THOMAS W., B.S., 2809 Hathaway Ter-
race, Wheaton, Md. 20906 (F-1, 4, 6)
MEBS, RUSSELL W., Ph.D., 6620 32nd St., N.,
Arlington, Va. 22213 (F-12, 20)
MELMED, ALLAN J., 732 Tiffany Court, Gaithers-
burg, Md. 20760 (F)
MELOY, THOMAS P., Ph.D., 5124 Baltan Rad.,
Sumner, Md. 20016 (F-14)
MENDELSOHN, MARK B., Psychology Dept.,
George Mason Univ., 4400 University Dr.,
Fairfax Va. 22030 (F-40)
MENIS, OSCAR, Analytical Chem. Div., Natl.
Bureau of Standards, Washington, D.C.
20234 (F)
MENZER, ROBERT E., Ph.D., 7203 Wells Pkwy.,
Hyattsville, Md. 20782 (F-4, 24)
MERRIAM, CARROLL F., Prospect Harbor,
Maine 04669 (F-6)
MESSINA, CARLA G., M.S., 9916 Montauk Ave.,
Bethesda, Md. 20034 (F)
MEYERHOFF, HOWARD A., Ph.D., 3625 S. Flor-
ence PI., Tulsa, Okla. 74105 (F-7)
MEYERSON, MELVIN R., Ph.D., A347, Polymer
Bg., National Bureau of Standards, Wash-
ington, D.C. 20234 (F-20)
MEYROWITZ, ROBERT, 1946 Overland Ave.,
#306, Los Angeles, Calif. 90025 (F)
MICHAEL, A. S., B.S., 7215 N. Magic Pl., Casas
Adobes W., Tucson, Ariz. 85704 (M-5, 6, 16,
24)
MICHAELIS, ROBERT E., National Bureau of
Standards, Chemistry Bldg., Rm. B316,
Washington, D.C. 20234 (F-20)
182
MIDDLETON, H. E., Ph.D., 430 E. Packwood, Apt.
H-108, Maitland, Fla. 32751 (E)
MIDER, G. BURROUGHS, M.D., Exec. Off., Amer.
Soc. Exper. Path. & Univ. Assoc. Res. & Educ.
Pathol., 9650 Rockville Pike, Bethesda, Md.
20014 (F)
MILLAR, DAVID B., NMRI, NNMC, Stop 36,
Physical Biochemistry Div., Washington,
D.C. 20014 (F)
MILLER, CARL F., P.O. Box 127, Gretna, Va.
24557 (E-6)
MILLER, CLEM O., Ph.D., 6343 Nicholson St.,
Falls Church, Va. 22044 (F-4, 6, 39)
MILLER, J. CHARLES, Ph.D., 10600 Eastborne
Ave., Apt. 7, W. Los Angeles, California 90024
(E-7, 36)
MILLER, PAUL R., Ph.D., ARS, USDA, Beltsville,
Md. 20705 (E-10)
MILLER, RALPH L., Ph.D., 5215 Abington Rd.,
Washington, D.C. 20016 (F-7)
MILLER, ROMAN R., 1232 Pinecrest Circle, Silver
Spring, Md. 20910 (F-4, 6, 28)
MILLIKEN, LEWIS T., SSL Res. Inst. 43-20,
NHTSA, 400 7th St., S.W., Washington, D.C.
20590 (M-1, 4, 6, 7)
MITCHELL, J. MURRAY, Jr., Ph.D., 1106 Dog-
wood Dr., McLean, Va. 22101 (F-6, 23)
MITCHELL, JOHN W., 9007 Flower Ave., Silver
Spring, Md. 20901 (F)
MITTLEMAN, DON, 80 Parkwood Lane, Oberlin,
Ohio 44074 (F-1)
MIZELL, LOUIS R., 108 Sharon Lane, Greenlawn,
N.Y. 11740 (F)
MOLINO, JOHN A., Ph.D., Sound Section, Nat.
Bureau Standards, Washington, D.C. 20234
(M-25)
MOLLARI, MARIO, 4527 45th St., N.W., Washing-
ton, D.C. 20016 (E-3, 5, 15)
MOLLER, RAYMOND W., Ph.D., Catholic Univ.
of America, Washington, D.C. 20017 (F-38)
MOORE, GEORGE A., Ph.D., Natl. Bur. of Stand-
ards 312.03, Washington, D.C. 20234 (F-6,
20, 29, 36)
MORRIS, J. A., 23-E Ridge Rd., Greenbelt, Md.
20770 (M-6, 15, 16)
MORRIS, JOSEPH BURTON, Chemistry Dept.
Howard Univ., Washington, D.C. 20001 (F)
MORRIS, KELSO B., Howard Univ., Washington,
D.C. 20059 (F-4, 39)
MORRISS, DONALD J., 102 Baldwin Ct., Pt. Char-
lotte, Fla. 33950 (E-11)
MOSTOFI, F. K., M.D., Armed Forces Inst. of
Pathology, Washington, D.C. 20306 (F)
MOUNTAIN, RAYMOND D., B318 Physics Bg.,
Nat. Bureau of Standards, Washington, D.C.
20234 (F)
MUEHLHAUSE, C. O., Ph.D., 9105 Seven Locks
Rd., Bethesda, Md. 20034 (F-1, 26)
MUELLER, H. J., 4801 Kenmore Ave., Alexandria,
Va. 22304 (F)
MUESEBECK, CARL F. W., U.S. Natl. Museum
of Nat. Hist., Washington, D.C. 20560 (E-3, 5)
MULLIGAN, JAMES H., Ph.D., 12121 Sky Lane,
Santa Ana, Calif. 92705 (F-13)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
MURDOCH, WALLACE P., Ph.D., Rt. 2, Gettys-
burg, Pa. 17325 (F-5, 24)
MURRAY, THOMAS H., 2915 27th St., N. Arling-
ton, Va. 22207 (M)
MURRAY, WILLIAM S., 1281 Bartonshire Way,
Potomac Woods, Rockville, Md. 20854 (F-5)
MYERS, ALFRED T., 11675 West 31st PI., Lake-
wood, Colo. 80215 (E-4, 6)
MYERS, RALPH D., Physics Dept., Univ. of Mary-
land, College Park, Md. 20740 (F-1)
N
NAESER, CHARLES R., Ph.D., 6654 Van Winkle
Dr., Falls Church, Va. 22044 (F-4, 7, 39)
NAMIAS, JEROME, Sc.D., 2251 Sverdrup Hall,
Scripps Institution of Oceanography, La
Jolla, Calif. 92037 (F-23)
NELSON, R. H., 7309 Finns Lane, Lanham, Md.
20801 (E-5, 6, 24)
NEPOMUCENE, SR. ST. JOHN, Villa Julie, Valley
Rd., Stevenson, Md. 21153 (E-4)
NEUENDORFFER, J. A., 911 Allison St., Alex-
andria, Va. 22302 (F-6, 34)
NEUSCHEL, SHERMAN K., 7501 Democracy
Blvd., Bethesda, Md. 20034 (F-7)
NEWMAN, MORRIS, Natl. Bur. of Standards,
.Washington, D.C. 20234 (F)
NEWTON, CLARENCE J., Ph.D., 1504S. 2nd Ave.,
Edinburg, Texas 78539 (E)
NICKERSON, DOROTHY, 4800 Fillmore Ave., Apt.
450 Alexandria, Va. 22311 (E-6, 32)
NIKIFOROFF, C. C., 4309 Van Buren St., Univer-
sity Park, Hyattsville, Md. 20782 (E)
NOFFSINGER, TERRELL L., Spec. Weather Serv.
Br., NOAA/NWS, Gramax Bldg., Silver Spring,
Md. 20910 (F-23)
NORRIS, KARL H., 11204 Montgomery Rad.,
Beltsville, Md. 20705 (F-27)
NOYES, HOWARD E., Ph.D., Assoc. Dir. Res.
Mgmt., WRAIR, Walter Reed Army Med. Ctr.,
Washington, D.C. 20012 (F-16, 19)
O
O’BRIEN, JOHN A., Ph.D., Dept. of Biology,
Catholic Univ. of America, Washington, D.C.
20064 (F-10)
O’CONNOR, JAMES V., 10108 Haywood Cir.,
Silver Spring, Md. 20902 (M-6, 7)
O’HARE, JOHN, Ph.D., 301 G St. S.W., Washing-
ton, D.C. 20024 (F-40)
O’HERN, ELIZABETH M., Ph.D., 633 G St., S.W.,
Washington, D.C. 20024 (M-16)
O’KEEFE, JOHN A., Code 640, Goddard Space
Flight Ctr., Greenbelt, Md. 20770 (F-1)
OEHSER, PAUL H., 9012 Old Dominion Dr.,
McLean, Va. 22101 (F-1, 3, 9, 30)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
OKABE, HIDEO, Ph.D., Rm. A-243, Bg. 222, Natl.
Bur. of Standards, Washington, D.C. 20234
(F-4)
OLIPHANT, MALCOLM W., Ph.D., Hawaii Loa
Coll., P.O. Box 764, Kaneohe, Oahu, Haw.
96744 (F)
ORDWAY, FRED, Ph.D., 5205 Elsmere Ave.,
Bethesda, Md. 20014 (F-4, 6, 28, 39)
ORLIN, HYMAN, Ph.D., Natl. Academy of Sci-
ences, 2101 Constitution Ave N.W., Wash-
ington, D.C. 20418 (F-17)
OSER, HANS J., Ph.D., 8810 Quiet Stream Ct.,
Potomac, Md. 20854 (F-6)
OSGOOD, WILLIAM R., Ph.D., 5101 Ridgefield
Rd., Rm. 108, Bethesda, Md. 20016 (E-14, 18)
OTA, HAJIME, M.S., 5708 64th Ave., E. Riverdale,
Md. 20840 (F)
OWENS, JAMES P., M.A., 14528 Bauer Dr., Rock-
ville, Md. 20853 (F-7)
)
PACK, DONALD H., 1826 Opalocka Dr., McLean,
Va. 22101 (F-23)
PAFFENBARGER, GEORGE C., D.D.S., ADA Res.
Unit, Natl. Bur. of Standards, Washington,
D.C. 20234 (F-21)
PAGE, BENJAMIN L., B.S., 1340 Locust Rd.,
Washington, D.C. 20012 (E-1, 6)
PARKER, KENNETH W., 6014 Kirby Rd.,
Bethesda, Md. 20034 (E-3, 10, 11)
PARKER, ROBERT L., Ph.D., Metallurgy Div.,
‘ Natl. Bur. of Standards, Washington, D.C.
20234 (F)
PARMAN, GEORGE K., 8054 Fairfax Rd., Alex-
andria, Va. 22308 (F-4, 27)
PARRY-HILL, JEAN, Ms., 3803 Military Rd.,
N.W., Washington, D.C. 20015 (M)
PATTI, JOGESH C., 8604 Saffron Dr., Lanham,
Md. 20801 (F)
PAYNE, FAITH N., 1745 Hobart St. N.W., Wash-
ington, D.C. 20009 (M-7)
PELCZAR, MICHAEL J., Jr., Vice Pres. for Grad.
Studies & Research, Univ. of Maryland, Col-
lege Park, Md. 20742 (F-16)
PEROS, THEODORE P., Ph.D., Dept of Chem-
istry, George Washington Univ., Washington,
D.C. 20006 (F-1, 4)
PETERLIN, ANTON, Polymers Div., Inst. Ma-
terials Res., Nat. Bureau Standards, Wash-
ington, D.C. 20234 (F)
PHAIR, GEORGE, Ph.D., 14700 River Rad.,
Potomac, Md. 20854 (F-7)
PHILLIPS, Mrs. M. LINDEMAN, M.S., 2510
Virginia Ave., N.W., #507N, Washington, D.C.
20037 (F-1,.6, 13,25)
PIKL, JOSEF, 211 Dickinson Rd., Glassboro, N.J.
08028 (E)
PITTMAN, MARGARET, Ph.D., 3133 Connecticut
Ave., N.W., Washington, D.C. 20008 (E)
PLAIT, ALAN O., M.S., 5402 Yorkshire St.,
Springfield, Va. 22151 (F-13)
183
POLACHEK, HARRY, 11801 Rockville Pike
Rd., Rockville, Md. 20852 (E)
POOS, F. W., Ph.D., 5100 Fillmore Ave.,
Alexandria, Va. 22311 (E-5, 6, 26)
POLLACK, Mrs. FLORA G., Mycology Lab., Rm.
11 North Bldg., Beltsville Ars. Ctr. W. Belts-
ville, Md. 20705 (F-10)
POPENOE, WILSON, Antigua, Guatemala, Cen-
tral America (E)
POWERS, KENDALL, Ph.D., 6311 Alcott Rd.,
Bethesda, Md. 20034 (F-15)
PRESLEY, JOHN T., 3811 Courtney Circle,
Bryan, Tx. 77801 (E)
PRESTON, MALCOLM 6&., 10 Kilkea Ct., Balti-
more, Md. 21236 (M)
PRINZ, DIANNE K., Ph.D., Code 7121.5, Naval
Res. Lab., Washington, D.C. 20375 (M-32)
PRO, MAYNARD J., 7904 Falstaff Rd., McLean,
Va. 22101 (F-26)
PRYOR, C. NICHOLAS, Ph.D., Naval Underwater
Systems Citr., Newport, RI. 02840 (F)
PURCELL, ROBERT H., 17517 White Grounds
Rd., Boyds, Md. 20720 (F)
PYKE, THOMAS N., Jr., Techn. Bg. A231, Nat.
Bur. Standards, Washington, D.C. 20234 (F)
R
RABINOW, JACOB, E. E., 6920 Selkirk Dr.,
Bethesda, Md. 20034 (F-1, 13)
RADER, CHARLES A., Gillette Res. Inst., 1413
Research Blvd., Rockville, Md. 20850 (F-4)
RADO, GEORGE T., Ph.D., 818 Carrie Court,
McLean, Va. 22101 (F-1)
RAINWATER, H. IVAN, Plant Protect. & Quaran-
tine Programs, APHIS, Fed. Center Bg. #1,
Hyattsville, Md. 20782 (E-5, 6, 24)
RAMIREZ-FRANKLIN, LOUISE, 2501 N. Florida
St., Arlington, Va. 22207 (M)
RAMSAY, MAYNARD, Plant Prot. Quar., APHIS,
USDA, Hyattsville, Md. 20780 (F)
RANEY, WILLIAM P., Code 102, Office of Naval
Research, Arlington, Va. 22217 (M)
RAUSCH, ROBERT, Dept. Microbiol., Western
College of Veterinary Medicine, U. of Sas-
katchewan, Saskatoon, Sask., Canada 57N
OWO (F-3, 15, 16)
RAVITSKY, CHARLES, M.S., 1808 Metzerott Rd.,
Adelphi, Md. 20783 (F-32)
READING, O. S., 6 N. Howells Point Rd., Bellport
Suffolk County, New York, N.Y. 11713 (E-1)
REAM, DONALD F., Holavallagata 9, Reykjavik,
Iceland (F)
RECHCIGL, MILOSLAV, Jr., Ph.D., 1703 Mark
Lane, Rockville, Md. 20852 (F-3, 4, 19)
REED, WILLIAM D., 3609 Military Rd., N.W.,
Washington, D.C. 20015 (F-5, 6)
REEVE, WILKINS, Ph.D., 4708 Harvard Rad.,
College Park, Md. 20740 (F-4)
REEVES, ROBERT G., Ph.D., U.S. Geol. Surv.,
EROS Data Ctr., Sioux Falls, So. Dak. 57198
(F-7, 36)
184
REGGIA, FRANK, MSEE, 6207 Kirby Rad.,
Bethesda, Md. 20034 (F-6, 13)
REHDER, HARALD A., Ph.D., U.S. Natl. Museum
of Nat. Hist., Washington, D.C. 20560 (F-3, 6)
REINER, ALVIN, B.S., 11243 Bybee St., Silver
Spring, Md. 20902 (M-6, 12, 13, 22)
REINHART, FRANK W., 9918 Sutherland Rd.,
Silver Spring, Md. 20901 (F-4, 6)
REINHART, FRED M., M.S., P.O. Box 591, Oak
View, Calif. 93022 (F-20)
REINING, PRISCILLA, Ph.D., 3601 Rittenhouse
St., N.W., Washington, D.C. 20015 (F-2)
REMMERS, GENE M., 7322 Craftown Rd., Fairfax
Station, Va. 22039 (M)
REVEAL, JAMES L., Ph.D., Dept. Botany, Univ.
of Maryland, College Park, Md. 20742 (F)
REYNOLDS, ORR E., Ph.D., Amer. Physiol. Soc.,
9650 Rockville Pike, Bethesda, Md. 20014 (F)
RHODES, IDA, Mrs., 6676 Georgia Ave., N.W.,
Washington, D.C. 20012 (F)
RHYNE, JAMES J., Ph.D., 15012 Butterchurn La.,
Silver Spring, Md. 20904 (F)
RICE, FREDERICK A., 8005 Carita Court,
Bethesda, Md. 20034 (F-4, 6, 16, 19)
RIOCH, DAVID McK., M.D., 2429 Linden Lane,
Silver Spring, Md. 20910 (F-3, 8)
RITT, P. E., Ph.D., GIE-Labs2 ing Sa sua
Rd., Waltham, Mass. 02154 (F-6, 13, 23, 29)
RIVLIN, RONALD S., Lehigh University, Bethle-
hem, Pa. 18015 (F)
ROBBINS, MARY LOUISE, Ph.D., George Wash-
ington Univ. Med. Ctr., 2300 Eye St. N.W.,
Washington, D.C. 20037 (F-6, 16, 19)
ROBERTS, ELLIOT B., 4500 Wetherill
Washington, D.C. 20016 (E-1, 6, 18)
ROBERTS, RICHARD B., Ph.D., Dept. Terrestrial
Mag., 5241 Broad Branch Rd., N.W., Wash-
ington, D.C. 20015 (F)
ROBERTS, RICHARD C., 5170 Phantom Court,
Columbia, Md. 21044 (F-6)
ROBERTSON, A. F., Ph.D., 4228 Butterworth PI.,
N.W., Washington, D.C. 20016 (F)
ROBERTSON, RANDAL M., Ph.D., 1404 Highland
Circle, S.E., Blacksburg, Va. 24060 (F-6)
ROCK, GEORGE D., Ph.D., The Kennedy Warren,
3133 Conn. Ave., N.W., Washington, D.C.
20008 (E)
RODNEY, WILLIAM S., 8112 Whites Ford Way,
Rockville, Md. 20854 (F-1, 32)
RODRIGUEZ, RAUL, 254 Torrs Sato, Baldrich,
Hato Rey, PR. 00918 (F-17)
ROLLER, PAUL S., 1440 N St., N.W., Apt. 208,
Washington, D.C. 20005 (E)
ROSADO JOHN A., 1709 Great Falls St., McLean,
Va. 22101 (F)
ROSE, WILLIAM K., Ph.D., 10916 Picasso Ln.,
Potomac, Md. 20854 (F)
ROSENBLATT, DAVID, 2939 Van Ness St., N.W.,
Apt. 702, Washington, D.C. 20008 (F-1)
ROSENBLATT, JOAN R., 2939 Van Ness St.,
N.W., Apt. 702, Washington, D.C. 20008 (F-1)
ROSENTHAL, JENNY E., 7124 Strathmore St.,
Falls Church, Va. 22042 (F-13, 32)
ROSENTHAL, SANFORD M., Bldg. 4, Rm. 122,
National Insts. of Health, Bethesda, Md.
20014 (E)
Rd.,
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
ROSS, FRANKLIN, Off. of Asst. Secy. of the Air
Force, The Pentagon, Rm. 4E973, Washing-
ton, D.C. 20330 (F-22)
ROSS, SHERMAN, National Research Council,
2101 Constitution Ave., N.W., Washington,
D.C. 20418 (F-40)
ROSSINI, FREDERICK D., Ph.D., Dept. Chemis-
try, Rice Univ., Houston, Tex. 77001 (F-1)
ROTH, FRANK L., M.Sc., 200 E. 22nd St., #33
(Roswell, NM. 88201 (E-6)
ROTH, ROBERT S., Solid State Chem. Sect.,
National Bureau of Standards, Washington,
D.C. 20234 (F)
ROTKIN, ISRAEL, 11504 Regnid Dr., Wheaton,
Md. 20902 (F-1, 13, 34)
ROWEN, JOHN W., Washington Towers #2407,
9701 Fields Rd., Gaithersburg, Md. 20760 (F)
RUBIN, MORTON J., M.Sc., World Meterol. Org.,
Casa Postale #5, CH-1211, Geneva 20,
Switzerland (F-23)
RUDOLPH, MICHAEL, 4521 Bennion Rad., Silver
Spring, Md. 20906 (M)
RUPP, N. W., D.D.S., American Dental Assoc.,
Research Division, National Bureau of Stand-
ards, Washington, D.C. 20234 (F-21)
RUSSELL, LOUISE M., Bg. 004, Agr. Res. Center
(West), USDA, Beltsville, Md. 20705 (F-5)
RYALL, A. LLOYD, Route 2, Box 216, Las Cruces,
N. Mex. 88001 (E-6, 10, 27)
RYERSON, KNOWLES A., M.S., Dean Emeritus,
15 Arlmonte Dr., Berkeley, Calif. 94707 (E-6)
S
SAALFIELD, FRED E., Naval Res. Lab., Code
6110, Washington, D.C. 20375
SAENZ, ALBERT W., Ph.D., Radiation Techn.
Div., Naval Research Laboratory, Code
66035, Washington, D.C. 20375 (F)
SAILER, R. I., Ph.D., 3847 S.W. 6TH PI., Gaines-
ville, Fla. 32607 (F-5)
SALLET, DIRSE W., 12440 Old Fletchertown Rd.,
Bowie, Md. 20715 (M-1, 14)
SANDERSON, JOHNA., Ph.D., 303 High St., Alex-
andria, Va. 22203 (F-1, 32)
SARIMENTO, RAFAEL, % UNDP, P.O. Box 400
GPO, Kaduna, Nigera (F)
SARVELLA, PATRICIA A., Ph.D., 12104 Dove
Cir., Laurel, Md. 20811 (F-6)
SASMOR, ROBERT M., 4408 N. 20th. Rd. Arling-
ton, Va. 22207 (F)
SAULMON, E. E., 202 North Edgewood St.,
Arlington, Va. 22201 (M)
SAVILLE, THORNDIKE, Jr., M.S., 5601 Albia Rd.,
Washington, D.C. 20016 (F-6, 18)
SAYLOR, CHARLES P., 10001 Riggs Rad.,
Adelphi, Md. 20783 (F-1, 4, 32)
SCHALK, JAMES M., Ph.D., 4600 Barbara Dr.,
Beltsville, Md. 20705 (F)
SCHECHTER, MILTON S., 10909 Hannes Court,
Silver Spring, Md. 20901 (F-4, 5, 24)
SCHINDLER, ALBERT I., Sc.D., Code 6000, U.S.
Naval Res. Lab., Washington, D.C. 20375
(F-1)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
SCHLAIN, DAVID, Ph.D., P.O. Box 348, College
Park, Md. 20740 (F-4, 20, 29, 36)
SCHMIDT, CLAUDE H., Ph.D., 1827 No. 3rd St.,
Fargo, No. Dak. 58102 (F-5)
SCHMITT, WALDO L., Ph.D., U.S. National
Museum, Washington, D.C. 20560 (E-3)
SCHNEIDER, SIDNEY, 239 N. Granada St.,
Arlington, Va. 22203 (E)
SCHNEPFE, MARIAN M., Ph.D., 2019 Eye St.,
N.W., #402, Washington, D.C. 20006 (F-4, 7)
SCHOEN, LOUIS J., Ph.D., 8605 Springdell PI.,
Chevy Chase, Md. 20015 (F)
SCHOENEMAN, ROBERT LEE, 9602 Ponca PI.,
Oxon Hill, Md. 20022 (F)
SCHOOLEY, ALLEN H., 6113 Cloud Dr., Spring-
field, Va. 22150 (F-1, 13, 23, 31)
SCHOOLEY, JAMES F., 13700 Darnestown Rad.,
Gaithersburg, Md. 20760 (F-1, 35)
SCHUBAUER, G. B., Ph.D., 5609 Gloster Rd.,
Washington, D.C. 20016 (F-1, 22)
SCHUBERT, LEO, Ph.D., The American Univ.,
Washington, D.C. 20016 (F-1, 4, 30)
SCHULMAN, FRED, Ph.D., 11115 Markwood Dr.,
Silver Spring, Md. 20902 (F-4)
SCHULMAN, JAMES H., Ph.D., U.S. Off. Naval
Res., Branch Off., 223 Old Marylebone
Rd., London, England NW1, 5TH (F-1, 32)
SCHWARTZ, ANTHONY M., Ph.D., 2260 Glen-
more Terr., Rockville, Md. 20850 (F-4)
SCHWARTZ, BENJAMIN, Ph.D., 888 Mont-
gomery St., Brooklyn, N.Y. 11213 (E)
SCHWARTZ, MANUEL, 321-322 Med. Arts Bg.,
Baltimore, Md. 21201 (M)
SCOTT, DAVID B., D.D.S., Dean, Case Western
Reserve Univ., Sch. of Dentistry, 2123 Abing-
ton Rd., Cleveland, Ohio 44106 (F-21)
SCRIBNER, BOURDON F., National Bureau of
Standards, Washington, D.C. 20234 (F-4, 32)
SEABORG, GLENN T., Ph.D., Lawrence Berkeley
Lab., Univ. of California, Berkeley, Caiif.
94720 (F-26)
SEEGER, RAYMOND J., Ph.D., 4507 Wetherill
Rd., Bethesda, Md. 20016 (E-1, 6, 30, 31)
SEITZ, FREDERICK, Rockefeller University, New
York, N.Y. 10021 (F-36)
SERVICE, JERRY H., Ph.D., Cascade Manor, 65
W. 30th Ave., Eugene, Oreg. 97405 (E)
SHAFRIN, ELAINE G., M.S., Apt. N-702, 800 4th
St., S.W., Washington, D.C. 20024 (F-4)
SHAPIRA, NORMAN, 86 Oakwood Dr., Dunkirk,
Md. 20810 (M)
SHAPIRO, GUSTAVE, 3704 Munsey St., Silver
Spring, Md. 20906 (F-13)
SHELTON, EMMA, National Cancer Institute,
Bldg. 37, Rm. 4C-06, Bethesda, Md. 20014 (F)
SHEPARD, HAROLD H., Ph.D., 2701 S. June St.,
Arlington, Va. 22202 (F-5, 24)
SHERESHEFSKY, J. LEON, Ph.D., 9023 Jones
Mill Rd., Chevy Chase, Md. 20015 (E)
SHERLIN, GROVER C., 4024 Hamilton St.,
Hyattsville, Md. 20781 (L-1, 6, 13, 31)
SHIELDS, WILLIAM ROY, A.M.S.S., 1 Deauville
Ct., Pikesville, Md. 21208 (F)
SHMUKLER, LEON, 817 Valley Forge Towers,
1000 Valley Forge Circle, King of Prussia, Pa.
19404 (F)
185
SHNEIDEROV, A. J., 1673 Columbia Rd., N.W.,
#309, Washington, D.C. 20009 (M-1, 22)
SHOTLAND, EDWIN, 418 E. Indian Spring Dr.,
Silver Spring, Md. 20901 (M-1)
SHROPSHIRE, W.,Jr., Ph.D., Radiation Bio. Lab.,
12441 Parklawn Dr., Rockville, Md. 20852
(F-6, 10, 33)
SHUBIN, LESTER D., Proj. Mgr. for Standards,
NILECJ/LEAA, U.S. Dept. Justice, Washing-
ton, D.C. 20530 (F)
SIEGLER, EDOUARD HORACE, Ph.D., 201 Tulip
Ave., Takoma Park, Md. 20012 (E-5, 24)
SILVER, DAVID M., Ph.D., Applied Physics Lab.,
Johns Hopkins Univ., Silver Spring, Md.
20910 (M-4, 6) ;
SIMHA, ROBERT, Ph.D., Case Western Reserve
Univ., Cleveland, Ohio 44106 (F)
SIMMONS, LANSING G., 3800 N. Fairfax Dr.,
Villa 809, Arlington, Va. 22203 (F-18)
SITTERLY, BANCROFT W., Ph.D., 3711 Brandy-
wine St., N.W., Washington, D.C. 20016
(E-d,.01, S2)
SITTERLY, CHARLOTTE M., Ph.D., 3711 Brandy-
wine St., N.W., Washington, D.C. 20016
(E-1, 6, 32)
SLACK, LEWIS, 106 Garden Rd., Scarsdale, N.Y.
10583 (F)
SLAWSKY, MILTON M., Ph.D., 8803 Lanier Dr.,
Silver Spring, Md. 20910 (F-6, 12, 22, 31)
SLAWSKY, ZAKA I., Ph.D., 9813 Belhaven Rad.,
Bethesda, Md. 20034 (F)
SLEEMAN, H. KENNETH, Ph.D., Div. Biochem.
WRAIR. Washington, D.C. 20012 (F)
SLOCUM, GLENN G., 4204 Dresden St., Ken-
sington, Md. 20795 (E-16, 27)
SMILEY, ROBERT L., 1444 Primrose Rd., N.W.,
Washington, D.C. 20012 (M-5)
SMITH, BLANCHARD DRAKE, M.S., 5265 Port
Royal Road, Springfield, Va. 22151
SMITH, DAYNA, 1745 Pimmit Dr., Falls Church
Va. 22043 (M)
SMITH, FLOYD F., Ph.D., 9022 Fairview Rad.,
Silver Spring, Md. 20910 (F-5, 24)
SMITH, FRANCIS A., Ph.D., 1023 55th Ave.,
South, St. Petersburg, Fla. 33705 (E-6)
SMITH, JACK C., 3708 Manor Rd., Apt. 3, Chevy
Chase, Md. 20015 (F)
SMITH, PAUL A., 4714 26th St., N., Arlington,
Va. 22207 (F-6, 7, 18, 22)
SMITH, ROBERT C., Jr., %Versar, Inc., 6621
Electronic Dr., Springfield, Va. 22151 (F-4, 22)
SNAVELY, BENJAMIN L., Ph.D., 721 Springloch
Rd., Silver Spring, Md. 20904 (F-6, 25, 32)
SNAY, HANS G., Ph.D., 17613 Treelawn Dr.,
Ashton, Md. 20702 (F-25)
SNOW, C. EDWIN, 14317 Chesterfield Rd., Rock-
ville, Md. 20853 (M-32)
SNYDER, HERBERT H., Ph.D., RFD. 1, Cobden,
IL. 62920 (F)
SOKOLOVE, FRANK L., 2546 Chain Bridge Rd.,
Vienna, Va. 22180 (M)
SOMERS, IRA I., 1511 Woodacre Dr., McLean,
Va. 22101 (M-4, 6, 27)
SOMMER, HELMUT, 9502 Hollins Ct., Bethesda,
Md. 20034 (F-1, 13)
186
SORROWS, H. E., Ph.D., 8820 Maxwell Dr.,
Potomac, Md. 20854 (F)
SPALDING, DONALD H., Ph.D., 17500 S.W. 89th
Ct., Miami, Fla. 33157 (F-6, 10)
SPECHT, HEINZ, Ph.D., 4229 Franklin St., Ken-
sington, Md. 20795 (E-1, 6)
SPENCER, LEWIS V., Box 206, Gaithersburg,
Md. 20760 (F)
SPERLING, FREDERICK, 1131 University Blvd.,
W., #1807, Silver Spring, Md. 20902 (F-19)
SPIES, JOSEPH R., 507 N. Monroe St., Arlington,
Va. 22201 (F-4, 19)
SPOONER, CHARLES S., Jr., M.F., 346 Spring-
vale Rd., Great Falls, Va. 22066 (F-1, 13, 25)
SPOONER, RONALD L., Ph.D., Planning Sys-
tems, Inc., 7900 Westpark Dr., McLean, Va.
22101 (M-25)
SPRAGUE, G. F., Ph.D., Dept. Agronomy, Univ. of
Illinois, Urbana, III. 61801 (E-33)
ST. GEORGE, R. A., 3305 Powder Mill Rd.,
Adelphi Station, Hyattsville, Md. 20783 (F-3,
5, 11, 24)
STAIR, RALPH, 1686 Joplin St. S., Salem, Ore.
97302 (E-6)
STAKMAN, E. C., Univ. of Minnesota, Inst. of
Agric., St. Paul, Minn. 55108 (E)
STALLARD, JOHN M., Ph.D., Hdgtrs., Naval
Material Command, MAT-035, Washington,
D.C. 20360 (F-6, 25)
STAUSS, HENRY E., Ph.D., 8005 Washington
Ave., Alexandria, Va. 22308 (F-20)
STEARN, JOSEPH L., 3511 Inverrary Dr., #108,
Lauderville, Fl. 33319 (E)
STEELE, LENDELL E., 7624 Highlange soc,
Springfield, Va. 22150 (F-20, 26)
STEERE, RUSSELL L., Ph.D., 6207 Carrollton
Ter., Hyattsville, Md. 20781 (F-6, 10, 19)
STEGUN, IRENE A., National Bureau of Stand-
ards, Washington, D.C. 20234 (F)
STEIDLE, WALTER E., 2439 Flint Hill Rd., Vienna,
Va. 22180 (F)
STEINER, BRUCE W., 6624 Barnaby St., N.W.,
Washington, D.C. 20015 (M)
STEINER, ROBERT F., Ph.D., 2609 Turf Valley
Rd., Ellicott City, Md. 21043 (F-4)
STEINHARDT, JACINTO, Ph.D., Georgetown
Univ., Washington, D.C. 20057 (F-4)
STEPHENS, ROBERT E., Ph.D., 4301 39th St.,
N.W., Washington, D.C. 20016 (E-1, 32)
STERN, KURT H., Ph.D., Naval Res. Lab., Code
6160, Washington, D.C. 20375 (F-4, 29, 30)
STEVENS, HENRY, 5116 Brookview Dr., Wash-
ington, D.C. 20016 (E)
STEVENS, RUSSELL B., Ph.D., Div. of Biological
Sciences, N.R.C., 2101 Constitution Ave.,
Washington, D.C. 20418 (F-10)
STEVENSON, JOHN A., 3256 Branoy Ct., Falls
Church, Va. 22042 (E-6, 10)
STEWART, KENNETH R., 12907 Crookston La.,
#16, Rockville, Md. 20851 (M-25)
STEWART, T. DALE, M.D., 1191 Crest Lane,
McLean, Va. 22101 (F-2, 6)
STIEBELING, HAZEL, K., 4000 Cathedral Ave.,
Washington, D.C. 20016 (E)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
STIEF, LOUIS J., Ph.D., Code 691, NASA God-
dard Space Flight Ctr., Greenbelt, Md. 20771
(F-4, 39)
STIEHLER, ROBERT D., Ph.D., Natl. Bur. of
Standards, Washington, D.C. 20234 (F-1, 4,
14, 39)
STILL, JOSEPH W., M.D., M.P.H., 1408 Edge-
cliff Lane, Pasadena, Calif. 91107 (E)
STILLER, BERTRAM, 1870 Wyoming Ave., N.W.
#604, Washington, D.C. 20009 (F-1)
STIMSON, H. F., 2920 Brandywine St., N.W.,
Washington, D.C. 20008 (E-1, 6)
STIRLING, MATHEW W., Mrs., 3311 Rowland PI.,
N.W., Washington, D.C. 20008 (F-2)
STOETZEL, MANYAB., Ph.D., 2600 Millvale Ave.,
North Forestville, Md. 20028 (F)
STRAUSS, SIMON W., Ph.D., 4506 Cedell PI.,
Camp Springs, Md. 20031 (F-4)
STRIMPLE, HARRELL, L., Dept. of Geology, The
Univ. of lowa, lowa City, IA. 52242 (M)
STUART, NEIL W., 1341 Chilton Dr.,
Spring, Md. 20904 (F-10)
SULZBACHER, WILLIAM L., 8527 Clarkson Dr.,
Fulton, Md. 20759 (F-16, 27)
SWICK, CLARENCE H., 5514 Brenner St., Capitol
Heights, Md. 20027 (F-1, 6, 12)
SWINGLE, CHARLES F., Ph.D., 431 Humboldt
St., Manhattan, Kans. 66502 (E-6, 10, 11, 33)
SYKES, ALAN O., 304 Mashie Dr., S.E., Vienna,
Va. 22180 (M-25)
Silver
+
TALBERT, PRESTON T., Dept. of Chem., Howard
Univ., Washington, D.C. 20059 (F)
TALBOTT, F. LEO, R.D. #4, Bethlehem, Pa.
18015 (F-1, 6)
TASAKI, ICHIJI, M.D., Ph.D., Lab. of Neuro-
biology, Natl. Inst. of Mental Health,
Bethesda, Md. 20014 (F)
TATE, DOUGLAS R., B.A., 11415 Farmland Dr.,
Rockville, Md. 20852 (F-1)
TAYLOR, ALBERT L., 2620 S.W. 14th Dr., Gaines-
ville, Fla. 32608 (E-15)
TAYLOR, B.N., Bg. 220, Rm. B258, Nat. Bureau
Standards, Washington, D.C. 20234 (F)
TAYLOR, JOHN K., Ph.D., Chemistry Bldg., Rm.
B-326, Natl. Bur. of Standards, Washington,
D.C. 20234 (F-4, 29)
~ TAYLOR, LAURISTON S., 7407 Denton Rad.,
Bethesda, Md. 20014 (E)
TAYLOR, LEONARD S., 706 Apple Grove Rad.,
Silver Spring, Md. 20904 (M)
TAYLOR, MODDIE D., Ph.D., 4560 Argyle Ter-
race, N.W., Washington, D.C. 20011 (F-4)
TCHEN, CHAN-MOU, City College of the City
Univ. of New York, New York, N.Y. 10031 (F)
TEAL, GORDON K., Ph.D., 5222 Park Lane,
Dallas, Tex. 75220 (F-6, 13, 29)
TEITLER, S., Code 4105, Naval Res. Lab.,
Washington, D.C. 20375 (F)
THAYER, T. P., Ph.D., U.S. Geological Surv.,
Mail Stop 954, Reston, Va. 22092 (F-7)
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
THEUS, RICHARD B., 8612 Van Buren Dr., Oxon
Hill, Md. 20022 (F)
THURMAN-SCHWARTZWELDER, E. B., 30 Ver-
sailles Blvd., New Orleans, La. 70125 (E)
TILDEN, EVELYN B., Ph.D., Calu Retirement
Dept., 12101 Lomas Blvd. N.E., #319, Albu-
querque, NM. 87112 (E)
TITUS, HARRY W., 7 Lakeview Ave., Andover,
N.J. 07821 (E-6)
TODD, MARGARET RUTH, Miss, P.O. Box 902,
Vineyard Haven, Mass. 02568 (F-7)
TOLHURST, GILBERT, Ph.D., 7 Red Fox Lane,
Amherst, Mass. 01002 (F-25, 40)
TOLL, JOHN S., Ph.D., Pres., State Univ. of New
York, Stony Brook, L.I., N.Y. 11794 (F-31)
TORRESON, OSCAR W., 4317 Maple Ave.,
Bethesda, Md. 20014 (E-6)
TOUSEY, RICHARD, Ph.D., Code 7140, Naval
Res. Lab., Washington, D.C. 20375 (F-1, 32)
TOWNSEND, MARJORIE R., B.E.E., 3529 Tilden
St., N.W., Washington, D.C. 20008 (F-6, 13, 22)
TRAUB, ROBERT, Ph.D., 5702 Bradley Blvd.,
Bethesda, Md. 20014 (F-5)
TREADWELL, CARLETON R., Ph.D., Dept. of
Biochemistry, George Washington Uhniv.,
2300 Eye St., N.W., Washington, D.C. 20037
(F-4, 19)
TRENT, EVAN M., Mrs., P.O. Box 1425, Front
Royal, Va. 22630 (M)
TRUEBLOOD, EMILY E., Ph.D., 7100 Armat
Dr., Bethesda, Md. 20034 (E-19)
TRUNK, GERALD, Ph.D., 503 Tolna St., Balti-
more, Md. 21224 (F)
TRYON, MAX, 6008 Namakagan Rd., Washing-
ton, D.C. 20016 (F-4, 6)
TUNELL, GEORGE, Ph.D., Dept. of Geol. Sci.,
Univ. of California, Santa Barbara, Calif.
93106 (E-7)
TURNER, JAMES H., Ph.D., 11902 Falkirk Dr.,
Potomac, Md. 20854 (F)
U
UHLANER, J. E., Ph.D., U.S. Army Res. Inst. for
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Arlington, Va. 22209 (F-40)
V
VACHER, HERBERT C., 19225 N. Cave Creek
Rd., No. 89, Phoenix, Arizona, 85024 (E)
VAN DERSAL, WILLIAM R., Ph.D., 6 S. Kensing-
ton St., Arlington, Va. 22204 (F-6)
VAN TUYL, ANDREW H., Ph.D., 1000 W. Nolcrest
Dr., Silver Spring, Md. 20903 (F-1, 6, 22)
VERGE} EFEIGHER- Ps re “PhD, Dept. ot
Chemistry, Univ. of Maryland, College Park,
Md. 20742 (F-4)
VIGUE, KENNETH J., Dir., Internatl. Projects, ITT
Corp., ITT Bldg., 1707 L St., N.W., Washing-
ton, D.C. 20036 (M-13, 31)
187
VINCENT, ROBERT C., Dept. Chem., George
Washington Univ., Washington, D.C. 20006
(F)
VINTI, JOHN P., Sc.D., 44 Quint Ave. 8, Allston,
MA. 02134 (F, 1, 6)
VISCO, EUGENE P., B.S., 2100 Washington
Ave., Silver Spring, Md. 20910 (M-1, 34)
VON BRAND, THEODOR C., M.D., Ph.D., 8606
Hempstead Ave., Bethesda, Md. 20034 (E-15)
VON HIPPEL, ARTHUR, 265 Glen Rd., Weston,
Mass. 02193 (E)
W
WACHTMAN, J. B., Jr., B. 306, Matls. Bldg.,
National Bureau of Standards, Washington,
D.C. 20234 (F)
WAGMAN, DONALD D., 7104 Wilson Lane,
Bethesda, Md. 20034 (F-4)
WAGNER, A. JAMES, NOAA Nat. Weather Serv.,
Nat. Meteorol. Ctr., W31, World Weather Bg.,
Washington, D.C. 20233 (F-23)
WALKER, E. H., Ph.D., 7413 Holly Ave., Takoma
Park, Md. 20012 (E-10)
WALTHER, CARL H., Ph.D., 1337 27th St., N.W.,
Washington, D.C. 20007 (F-6, 18)
WALTON, W. W., Sr., 1705 Edgewater Pkwy.,
Silver Spring, Md. 20903 (F-4, 6, 41)
WARGA, MARY E., 2475 Virginia Ave., N.W.,
Washington, D.C. 20037 (F-32)
WARING, JOHN A., 8502 Flower Ave., Takoma
Park, Md. 20012 (M-12, 30)
WATERWORTH, HOWARD E., Ph.D., 10001
Franklin Ave., Seabrook, Md. 20801 (F)
WATSON, BERNARD B., Ph.D., 6108 Landon La.,
Bethesda, Md. 20034 (F-6, 31)
WATSON, ROBERT B., 1167 Wimbledon Dr.,
McLean, Va. 22101 (M-13, 25, 31, 32)
WAYNANT, RONALD W., Ph.D., 13101 Claxton
Dr., Laurel Md. 20811 (F-6, 13, 32)
WEAVER, E. R., 6815 Connecticut Ave., Chevy
Chase, Md. 20015 (E-4, 6)
WEBB, HAMILTON B., Chief, Health Services,
Library Congress, Washington, D.C. 20540
(M-6)
WEBS; RAEPH ES Ph.D: 21\P* ‘Ridge “Ad:
Greenbelt, Md. 20770 (F-5, 24)
WEBB, RAYMON E., Agr. Res. Center, USDA,
Beltsville, Md. 20705 (M)
WEBER, EUGENE W., B.C.E., 2700 Virginia Ave.,
N.W., Washington, D.C. 20037 (F-6, 12, 17, 18)
WEBER, ROBERT S., Box 142, Harlingen, TX.
78550 (M-6, 13, 17)
WEIDA, FRANK, 19 Scientists Cliff, Port Repub-
lic, Calvert County, Md. 20676 (E-1)
WEIDLEIN, E. R., Weidacres, P.O. Box 445,
Rector, Pa. 15677 (E)
WEIHE, WERNER K.,2103 Basset St., Alexandria,
Va. 22308 (F-32)
WEINBERG, HAROLD P., B.S., 1507 Sanford Rad.,
Silver Spring, Md. 20902 (F-20)
188
WEINTRAUB, ROBERT L., 305 Fleming Ave.,
Frederick, Md. 21701 (F-4, 10, 16, 33)
WEIR, CHARLES E., Rt. 3, Box 260B, San Louis
Obispo, Calif. 93401 (F)
WEISS, ARMAND B., D.B.A., 6516 Truman Lane,
Falls Church, Va. 22043 (F-34)
WEISS, MICHAEL S., 17609 Cashell Rd., Rock-
ville, Md. 20853 (M-25)
WEISSBERG, SAMUEL, 14 Granville Dr., Silver
Spring, Md. 20901 (F-1, 4)
WEISSLER, ALFRED, Ph.D., 5510 Uppingham
St., Chevy Chase, Md. 20015 (F-1, 4, 25)
WELLMAN, FREDERICK L., Dept. of Plant
Pathology, North Carolina State Univ.,
Raleigh, N.C. 27607 (E)
WENSCH, GLEN W., Esworthy Rd., Rt. 2, Ger-
mantown, Md. 20767 (F-6, 20, 26)
WEST, WILLIAM L., Dept. of Pharmacology,
College of Medicine, Howard Univ., Washing-
ton, D.C. 20059 (M-19, 26, 39)
WETMORE, ALEXANDER, Ph.D., Smithsonian
Inst., Washington, D.C. 20560 (F-3, 6)
WEXLER, ARNOLD, Phys. B 328, Natl. Bur. of
Standards, Washington, D.C. 20234 (F-1, 35)
WHERRY, EDGAR T., Ph.D., 41 W. Allens La.,
Philadelphia, Pa. 19119 (E)
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WHITTEN, CHARLES A., 9606 Sutherland Rd.,
Silver Spring, Md. 20901 (F-1, 6)
WICHERS, EDWARD, 9601 Kingston Rd., Kens-
ington, Md. 20795 (E)
WIENER, ALFRED, B.S., USDA Forest Service,
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D.C. 20250 (F-11)
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Va. 22203 (F-1, 22, 31, 35)
WILHELM, PETER G., 6710 Elroy Pl., Oxon Hill,
Md. 20021 (F)
WILLENBROCK, F. KARL, Director, Inst. for Appl.
Tech., Natl. Bur. Standards, Washington
D.C. 20234 (F)
WILLIAMS, DONALD H., 4112 Everett St., Kens-
ington, Md. 20795 (M)
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204, Tucson, Ariz. 85711 (F-1, 6)
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McLean, Va. 22101 (F-4)
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WOLFF, EDWARD A., 1021 Cresthaven Dr., Silver
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Affairs, University of Washington, Seaittle,
Washington 98195 (F)
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_ Potomac, Md. 20854 (M)
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Silver Spring, Md. 20902 (F-4, 19)
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Standards, Washington, D.C. 20234 (E-1, 4)
WOOD, MARSHALL K., M.P.H., P.O. Box 27,
Castine, Me. 04421 (F)
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Arlington, Va. 22201 (F-4, 29)
WORKMAN, WILLIAM G., M.D., 5221 42nd St.,
N.W., Washington, D.C. 20015 (E-6, 8)
WULF, OLIVER R., Noyes Lab. of Chem. Phys.,
Calif. Inst. of Tech., Pasadena, Calif. 91125
(E)
Y
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Rd., Oxon Hill, Md. 20022 (M-23)
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J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
YODER, HATTEN S., Jr., Geophysical Lab., 2801
Upton St., N.W., Washington, D.C. 20008
(F-4, 7)
YOLKEN, H. T., 8205 Bondage Dr., Laytonsville,
Md. 20760 (F-29)
YOUNG, BOBBY G., Dept. of Microbiology, Univ.
of Maryland, College Park, Md. 20742 (M-16)
YOUNG, DAVID A., Jr., Ph.D., 612 Buck Jones
Rd., Raleigh, N.C. 27606 (F-5)
YOUNG, M. WHARTON, 3230 Park PI., Washing-
ton, D.C. 20010 (F)
YUILL, J. S., M.S., 4807-A Hartwick Rd., College
Park, Md. 20740 (E-5, 6, 24)
Z
ZELENY, LAWRENCE, Ph.D., 4312 Van Buren
St., University Park, Hyattsville, Md. 20782 (E)
ZIES, EMANUEL G., 3803 Blackthorne St., Chevy
Chase, Md. 20015 (E-4, 6, 7)
ZOCH, RICHMOND T., 12642 Craft Lane, Bowie,
Md. 20715 (F)
ZON, GERALD, Dept. Chemistry, Catholic Univ.
of America, Washington, D.C. 20064 (M)
ZWEMER, RAYMOND L., Ph.D. 3600 Chorley
Woods Way Silver Spring, Md. 20906 (E)
189
—NOTICE—
Tape cassettes of the Symposium are still available. The cost is $10.00 per hour. Minimum
order 30 minutes. Use this form to order. Cassettes will be made and mailed to you in
2 weeks from receipt of this form. Note: Not all of these papers are available in published
form.
ORDER FORM FOR TAPE CASSETTES
Symposium—Energy Recovery from Solid Wastes
Approx No.
Keynote Session of Minutes
ey a HARVEY ALTER: Introduction to the Symposium....... 15
_ ay ee RIGHARD Ll. EESHER= Keynote address -2)..'...-.-..... 30
Session 1—Refuse Derived Fuel
ee 3 DAVID L. KLUMB: Union Electric’s Solid Waste Utilization
S\ASIIGIG) Gio 5 68 as cea ech penn nC 30
my 4 DR. NATE SNYDER: Fuel From Refuse for Utilities .. 30
ae |} VISCOMI, ET AL.: Feasibility Study for Burning RDF in
Dl Ca tO IPE PAG ©) actly secrete zara an Temaelanir a ak ee ava 30
a 6 WILLIAM DELL: The CPU-400 Gas Turbine System ..... 30
Session 2— Steam Generation from Waste
a W. K. MACADAM: The Design and Pollution Control
Peas OlmeMesNES CO ee 8k a) succeed este aes gene 30
pe #8 MAURICE J. WILSON: The Markets for and the Economics
Crile AMEN CLOVE catia seco ie cuss 5 Aone eee acs mo mieus 2'@ 000s Gree a 30
ay 9 BRUCE PYEE: Akron s Recycle Energy system ......... - 30
#F 10 JACK ADAMS: Red Lion Energy Recovery Project ...... 30
Session 3—Biological Conversion
ee 11 LOUIS SPANO: Enzymatic Conversion of Cellulosic Wastes
WOK GIN COS SUSE Es ct Oe ee tea era ae eer 30
me Ff 12 KISPERT, ET AL.: An Evaluation of Methane Production
PROMMOO MCR ASIC Rowe rc sty ccs cone a a see oe ek es 30
mos 13 PFEFFER, ET AL.: Energy From Refuse by Bioconversion-
ReMMeMUAMOMN eee cee re tae ee eke lees enw eia las 30
oe # 14 DISCWSSION re ee os. et eee Su teen 45
Session 4—After Dinner Address
a #15 ORs ALERTED) 1 Cl GEL Gos | ipa ere ar are ee 45
Session 5—Pyrolysis of Wastes to Oils and Gases
= # 16 T. DONEGAN: A Summary of the Performance of the
PUROXDemonstration Plant .5-)2.55-26.2.+- 62.6.2 30
ee 17 JOHN STOIA: TORRAX—A Slagging Pyrolysis System for
| COMMUN Sse Rete on Sak a oe dG t 30
ma * 18 EDSEL STEWART: Landgard System for Energy Re-
COWEN cia. eig hc ee APO eS Agi eee eae ee 30
= # 19 GEORGE MALLAN: Garret Oil Conversion Pyrolysis
SV GUST Sa ene re ne er nae 30
mo #F 20 DiS CW SSION re eto e eae caves eee ea ebot etme = 30
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976 191
Session 6—Conversion of Wastes to Protein
chee Ha? | CHARLES ROGERS: Problems and Potentials Associated
withthe: Productionins: webs We eee ee Sek ene 30
me R.C. RIGHELATO: Microbial Protein from Agricultural
Wastes- ooo sie occ ho eid oe wake «ot ais os seem eee ee 30
ee GENE WEISBERG, ET AL.: Engineering Design and Eco-
nomic Feasibility of a Feedlot Waste Bio-Conversion
SVSICIN «cafe cueg oe be pin, oe eaves cate esl ee 30
Session 7—Specialized Wastes and Energy Recovery
ee sw GEORGE INGLE: Energy Recovery From Paint Sludges
and Miaste: Plasticsy:a20-s(cte sens h «SEU oh, Ate 30
Peg 5 HENRY JOHNSON: Wastes as Fuel for Industry ....... 30
Ae 26 ERWIN C. MOATS: Operation of the Goodyear Tire
Fired Oiler 025: deadt ducobsailt ee eee a0 eee 30
saree awd DISCUSSION coe Ova besae @ nas ated nen 45
NAME:
ADDRESS FOR MAIL:
ADDRESS FOR BILLING:
)
192 J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
|
:
:
Acknowledgments for Symposium
The publication costs of this issue were met in
part through grants supplied by the Environmen-
tal Protection Agency and the Federal Highway
Administration of the Department of Transpor-
tation.
For recording the Symposium we acknowledge
the assistance of David S. Garber, a specialist in
corporate life development recording. As an in-
dustrial personnel specialist he has had wide ex-
perience recording and communicating every
J. WASH. ACAD. SCI., VOL. 66, NO. 3, 1976
: Energy Recovery from Solid Wastes
phase of corporate life from human _ factor
changes in top management personnel to produc-
ing, indexing and editing minute-by-minute
archival recordings of important meetings and
symposia.
Richard H. Foote, Editor
Elizabeth Ostaggi, Editorial Assistant
193
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NAN PED)
Women
Chemists
NATIONAL SCIENCE
FOUNDATION PROGRAM
The National Science Foundation in an attempt to
tap the underutilized resource which women repre-
sent has funded a series of projects under their
Women in Science Program, whose objective is to
develop and test methods to attract and retain
women in scientific careers.
The Science Career Facilitation Project grants
are aimed at women who received bachelor’s or
master’s degrees in science between 2 and 15 years
ago and who are not presently employed in the fields
for which they were trained. The women selected
to participate in the project will be provided with an
educational experience designed to increase their
level of knowledge to that expected of a current
graduate at the same degree level. Participants se-
lected for these projects will be expected to be pre-
pared, at the end of their training to enter directly
into graduate training or employment.
These grants provide funding for educational
costs only; no funds are provided for stipends or
travel.
THE AMERICAN UNIVERSITY
PROGRAM
The American University Chemistry Program will
be current topics from organic, physical, analytical
and biochemistry with approximately seven weeks
in each area. The topics will be taught by the faculty
of The American University assisted by outside con-
sultants in selected areas.
The program will include both theoretical and
experimental developments of the last fifteen years
designed to bring the participants up-to-date on
current thinking in each area. The heavy emphasis
on laboratory skills should provide substantial ex-
perience whether the individual takes a job in gov-
ernment or industry or enters graduate school.
The American University Program will be a
twenty-eight week program beginning October 5,
1976 and ending May 13, 1977. The program will
meet five days a week Monday through Friday from
10:00 a.m. until 2:00 p.m. and will normally be one
hour of lecture and three hours of laboratory per day.
COSTS
The costs for the faculty and supplies are covered
by the grant from the National Science Foundation.
Therefore there is no charge for the program to the
participants.
There is no university course credit for the pro-
gram. However each participant will receive a cer-
tificate and letter indicating the topics covered and
the numbers of hours completed in the program.
APPLICATION DEADLINE
Twenty participants will be selected for the pro-
gram on the basis of the applications submitted no
later than September 3. Participants selected will be
notified by September 15. An application form is
enclosed.
Application forms and transcripts should be sent
to:
Dr. Nina M. Roscher
Women in Science Program
Department of Chemistry
The American University
Washington, D. C. 20016
WOMEN IN CHEMISTRY PROGRAM
Project Director: Dr. Nina M. Roscher
Associate Professor of Chemistry
B.S. University of Delaware
Ph.D. Purdue University
Faculty
Dr. Mary Aldridge
Professor of Chemistry
B.S. University of Georgia
M.A. Duke University
Ph.D. Georgetown University
Dr. Frederick W. Carson
Associate Professor of Chemistry
B.S. Massachusetts Institute of Technology
M.A. Washington University
Ph.D. University of Chicago
Dr. Paul F. Waters
Professor of Chemistry
B.S. University of Scranton
Ph.D. Rutgers, The State University
Dr. Thomas Cantrell
Associate Professor of Chemistry
B.S. University of Southern California
M.S. University of Southern California
Ph.D. Ohio State University
For information call the Project Director at
202 —686-2445
(94
yen) ae
ant mdi) ray)
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Pp2W22
VOLUME 66
Number 4
Journal of the DECEMBER, 1976
WASHINGTON
ACADEMY .. SCIENCES
Issued Quarterly
at Washington, D.C.
CONTENTS
Feature:
EDWARD S. AYENSU: Alternatives for Biological Resources in Africa ...
Profile:
ASHLEY B. GURNEY: A Polish Naturalist in Peru: The Life and Work
lM e USAW ONIUKOMISIG oe core eee ls eae tan vnle sc) wale a obamae aie led ianiue
Research Reports:
T. J. FREST, H. L. STRIMPLE, and M. R. McGINNIS: A New Species
of Platycystites (Echinodermata: Paracrinoidea) From the Middle
Ordovician of Oklahoma
T. J. FREST and H. L. STRIMPLE: Evolutionary and Paleoecologic Signifi-
-eance of Abnormal Platycystites cristatus Bassler (Echinodermata:
AAC TER ONG CAN sh es eee AE A aot 2 gear Tae, a Jem OM slap 221
L. C. KNORR, H. C. PHATAK, and H. H. KEIFER: Web-Spinning Erio-
(LAG. YORUMCIES pa a se NS ay ts rem on ene rer ef, ee SO DR 228
W. R. HEYER and M. H. MUEDEKING: Notes on Tadpoles as Prey for
INeticigl smc pslitnithe Sos ies, torte een amen te te clin aN ata wee mayen dred tyes 235
P. WILLEY and D. H. UBELAKER: Notched Teeth from the Texas
JP evra ey gi Nee ea allo Metab eae he ESTE 4 AO tt nD aI eo 0 ge CP CEP ne ORO a Rene
Academy Affairs:
Board of Managers Meeting Notes—February 25, 1976...................
INSERTION ttle Rae ie ie eae ay tp et gee aie nee Mage ae "ce ne ee 248
Selene’ Ae te NEWS ache ees owed ores ya "e aoe oe ONDA ae 249
FAAMNOUNCEMENtS 0.5. cache ke bce cee es ff cht lene oe Mant Oa ee tet ores 196, 246
SS L/BRARIES
Washington Academy of Sciences
EXECUTIVE COMMITTEE
President
Florence H. Forziati
President-Elect
Riciu.ard H. Foote
Secretary
Nelson W. Rupp
Treasurer
Mary H. Aldridge
Members at Large
George Abraham
Grover C. Sherlin
BOARD OF MANAGERS
All delegates of affiliated
Societies (see facing page)
EDITOR
Richard H. Foote
EDITORIAL ASSISTANT
Elizabeth Ostaggi
ACADEMY OFFICE
9650 Rockville Pike (Bethesda)
Washington, D.C. 20014
Telephone (301) 530-1402
Published quarterly in March, June, September, and December of each year by the
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postage paid at Washington, D.C. and additional mailing offices.
Founded in 1898
The Journal
This journal, the official organ of the Washington Aca-
demy of Sciences, publishes historical articles, critical
reviews, and scholarly scientific articles; proceedings
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The Journal appears four times a year (March, June,
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Back Issues
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(1898-1910) Index: To Vols. 1-13 of the Proceedings
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DELEGATES TO THE WASHINGTON ACADEMY OF SCIENCES,
REPRESENTING THE LOCAL AFFILIATED SOCIETIES
Biivimsap ical: SOCiety Of WashiMgtOMl (5.62645 t05 6h cee ocd aie se ey ms ae oes oe wo Me James F. Goff
Panag aocical Society Of WasDINGlON: 2. 2.2.5 6.2 ts o be dds se Ee See koe owe ee oe Jean K. Boek
een ee MES OCICIVTOr WASMINCLOME re a6. 2. ses ec lec oes Pee ee ee ae Ba ewe Inactive
enEMmie AESOCIeDY Ol WASHINGTON. . ss... oshcc os... eee es ee ee de ee eaves Delegate not appointed
Emmonmarocical Society Of Washington .....:.<...s2--5 62 eee e eb eb ba hese eee ee eee Maynard Ramsay
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Delegates continue in office until new selections are made by the representative societies.
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976 195
ANNOUNCEMENT
BELTSVILLE SYMPOSIUM II: BIOSYSTEMATICS IN AGRICULTURE
BELTSVILLE AGRICULTURAL RESEARCH CENTER
BELTSVILLE, MARYLAND
MAY 9-11, 1977
In 5 symposium sessions leading investigators will lecture or engage
in panel discussions on the role that biosystematics has in agriculture.
Main topics will include new techniques, taxonomic theories, uses of
taxonomic and biosystematic data, especially predictive applications,
and the planning and direction of biosystematic research. In addition,
a poster session and mixer is scheduled for the evening of May 9.
Manned displays at the mixer should generate valuable discussion.
For further information, send lower portion of this notice to:
Dr. James A. Duke
Publicity Committee, BARC Symposium II
Plant Taxonomy Laboratory
Room 117, Bldg. 001, BARC West, USDA
Beltsville, Maryland 20705 U.S.A.
BELTSVILLE SYMPOSIUM II: BIOSYSTEMATICS
IN AGRICULTURE
Please send further information on the Symposium to:
NAME
ADDRESS
196 J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
FEATURE
Alternatives for Biological Resources in Africa’
Edward S. Ayensu
Director, Endangered Species Program, National Museum of Natural History,
ABSTRACT
This paper calls attention to the fact that most of the current basic food items that
feature in the diets of African homes were historically recent introductions to that
continent. Attention is directed to the need for the development of the underexploited
plants and animals that seem to have economic potential. The local sources of plant
and animal proteins including fish proteins are discussed. Observations are made on
the changing food habits of the people on the African continent. The need for sub-
stantial research in the biological resources of the continent are discussed.
Over the years I have become painfully
aware of the fact that we in Africa
have been making very little use of the
biological resources available on our con-
tinent. In fact, the current use of only
a few of the many biological resources
with which Africa is endowed is a re-
flection of our inactivity in exploring
the new and alternative resources of this
magnificent part of the world. I would
venture to say that since the Neolithic
practically no new major food item
emanating from the African flora has
been added to the diet of the people.
I had the good fortune of being ap-
pointed the Co-Chairman of the U. S.
Academy of Science’s panel on ‘‘Under-
exploited Tropical Plants of Promising
Economic Value’’ in March 1974. The
work of the panel culminated in the
gathering of an unbelievable amount of
information on the many plants that
people in the third world have not been
‘Paper presented at the Seminar for African
Alternatives at the National Assembly, Senegal,
from 4—6 February 1976.
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
using to their best advantage. The panel
was charged with three main objectives:
to identify neglected but seemingly useful
tropical plants, both wild and domesti-
cated, that have economic potential; to
select the plants that showed the most
promise for wider exploitation through-
out the tropics; and to indicate the
requirements and avenues for research
that will ensure that selected plants
reach their fullest potential.
I offer these same objectives to African
scientists as a basis for seeking alterna-
tives for the judicious exploitation of our
biological resources.
Of the approximately 40,000 species of
plants that occur in Africa, only a small
number have been used throughout
human history. Furthermore, of the
handful of crops that form the bulk
staples, a significant portion consists of
plants that are not native to Africa.
For example, the tropical root crop
cassava (Manihot esculenta), an im-
portant carbohydrate source in the diet
of many African people today, is a native
of Brazil, from whence it spread to other
197
parts of Latin America and the rest of
the tropical areas of the world. The
groundnut (Arachis hypogaea), which is
rich in non-drying oil and protein as well
as vitamins B and E, is also a native
of South America. It was the Portuguese
who introduced the plant from Brazil
to West Africa in the 16th Century. The
sweet potato (Ipomoea batatas), with
its edible tubers and tender leaves, is
likewise a native of tropical America.
Ethnobotanical records show that the
sweet potato was grown in Mexico and
many parts of Central and South America
during pre-Columbian times but was
unknown in Africa, Asia, and Europe
during the same period. The cocoyam
(Zanthosoma sagittifolium) is a native of
tropical America. Although the Portu-
guese and the Spanish had known about
this plant, it was not until 1841 that
missionaries from the West Indies intro-
duced it to Ghana. Rice (Oryza sativa),
which plays a very important role in the
diet of Africa, traces its origin to south-
east Asia. Once again it was the Portu-
guese who introduced rice into Brazil
and West Africa. Maize (Zea mays) is
undoubtedly one of the most important
cereals in the African diet today. Like
most of the above-mentioned cultivated
plants, maize is not native to Africa. The
plant was in cultivation in the New World
during pre-Columbian times. Maize in its
present form has never been found grow-
ing in a wild state anywhere. There is
very reliable evidence that maize did not
reach the Old World (including Africa)
before 1492.
Of the commercially) important cash
crops that are grown in Africa, cocoa
(Theobroma cacao) is perhaps the most
important— certainly for Ghana, Nigeria
and the Ivory Coast. I hope you will not
be too surprised to learn that, again,
the cocoa tree is a native of tropical
South America. The plant was introduced
to the islands in the Gulf of Guinea in
the 17th Century by the Spanish and
Portuguese. A few cocoa pods of the
Amelonado variety were taken to Ghana
in 1879 from Fernando Po and, as you
are all aware, these few pods gave rise
198
to a very important industry in a major
portion of West Africa. Another cash
crop that features prominently in the
industrial activity of some African coun-
tries is para rubber (Hevea brasiliensis).
As its scientific name suggests, this plant
originated in the tropical rain forests of
the Amazon basin in South America.
I could go on and on citing examples
of a number of other crops that are
currently used in Africa but have their
origins elsewhere. I do not want to leave
you with the impression that Africa has
not contributed something to other coun-
tries. For example, sorghum, which is of
African origin, was introduced to China
early in human history. This crop is now
widely distributed in China because of
the development of several local varieties.
Nevertheless it is a sobering feeling to
visualize what our dietary situation might
have been on this continent if all the
foreign crops I have mentioned were not
available to us today. I feel uncomforta-
ble even to think of the striking readjust-
ments in our lives that would be neces-
sary if we had not been exposed to all
these introductions.
Why is it that throughout our history
we have made but little use of our bio-
logical resources? The answer to this
loaded question should be viewed from
an historical perspective. During the
colonial era very little attention was
given to scientific research on the many
indigenous plant and animal species that
may be of promising economic value,
because the consumer demands of the
metropolitan countries of Europe were
the principal determinants of the agrarian
practices encouraged in the colonies.
The scientific research institutes that
were established in a number of African
countries during the colonial era were
slanted to fulfill specific missions. For
example, many of the research organisa-
tions established by the British and the
French in West Africa were mainly con-
cerned with problems connected with the
production of raw materials for export
to the colonial and other European and
North American markets. As I pointed
out during my presentation to the West
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
African Science Association Conference
here in Dakar some two years ago, the
research efforts of the science institutes
in Africa have not changed materially
since the attainment of independence.
The same mentality that guided research
activities in Africa before political inde-
pendence is being perpetuated today.
Furthermore, several food items that
were featured in the diets of Africans
before the coming of the Europeans
have been discarded gradually and
replaced by kinds of foods that are
readily acceptable to Europeans. It is
only in relatively recent years that
Africans have become proud to present
indigenous dishes to their foreign visitors.
Apart from the colonial influence on
agricultural research priorities in Africa,
there is a fundamental attitude towards
agriculture that separates, for example,
the American Indian farmer from the
African farmer. Historically the Central
and South Americans of Mexico and
Peru (to mention but two countries)
were more interested in developing dif-
ferent strains of crops while their African
counterparts were interested in the
domestication of animals. And, as Afri-
can civilization progressed, animals often
became the equivalent of money, e.g.
cattle culture in Rwanda.
Another limiting factor in the proper
exploitation of our plant resources has
been the quality of African soils. By and
large, the soils of Africa are poor. You
are all familiar with the typical weather-
ing processes of our soils that often
result in the formation of hard, reddish
clay soils commonly known as laterite.
Lateritic soils develop when the fertile
topsoil is eroded away by the intensive
rainstorms that expose the red clay soils
underneath to the high solar radiation
that often follows a big downpour of rain
in the tropics. In the arid regions of
Africa, wind erosion results in the re-
moval of the fertile topsoil and renders
the land unsuitable for efficient agricul-
tural use. Over-grazing in certain parts of
Africa has resulted in more serious abuse
of the land than have other causes of
soil erosion. The browsing habits of
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
goats, for example, are very familiar
to many of you. Until marked soil con-
servation measures are taken to safe-
guard the land, we cannot begin to think
seriously about the efficient use of the
limited suitable farmlands that are still
available in Africa.
I think it is very important for us to
understand that soil biology is a crucial
component in the assessment of our
biological resources because it is the
basis of virtually all plant life, and hence
all faunal elements depend on it as well.
In a sense the soil is the most important
biological medium since its composition
includes both organic and inorganic sub-
stances. I need not remind you that our
lack of knowledge of tropical soil was
the principal reason for the Groundnut
Scheme failure. It is, therefore, important
that throughout our assessment of the
biological resources of Africa, we bear in
mind the state of our soils.
Plant Protein Production
When I began to reflect on the alterna-
tives for biological resources in Africa,
my mind immediately centered around
the problems of protein production for
food. Of all the possible sources for
protein, I consider plants the most
important. Plant proteins are basically
cheaper than animal proteins. Let us
first consider edible leaves of tropical
origin. Proteins are first created in leaves.
The process of photosynthesis is prin-
cipally responsible for the creation of
many intermediate reactions such as the
production of keto acids. Briefly, soluble
nitrogenous compounds and minerals are
brought to the leaves where the ammonia
portion is combined directly with the keto
acids to form amino acids, which lead to
the process of building-up of protein
aggregates. From the standpoint of nu-
trition, there is no excuse for the diet
of the African people to be short of pro-
teins, because edible green leaves are
abundant on the continent. The green
leaves are rich in proteins but, in addi-
tion, they are physiologically important
as regulators of the digestive tract. The
green leaves also contain important
199
vitamin and mineral components that
offer further enrichment to diets that
are basically starch-based. Vitamin A is
often found in large quantities in dark
green leaves and is often resistant to
the effects of cooking. Vitamin C, which
is also present in leaves in appreciable
quantities, often tends to be destroyed
by cooking. Vitamin B, which is soluble
in water, tends to be lost when cooking
water is discarded. Other ingredients
such as riboflavin and thiamine occur in
reasonable quantities in leaves.
If I may digress a moment, just before
I visited the People’s Republic of China
in July 1975, I was invited to dinner by
the Chinese Ambassador in Ghana. At
dinner several delicious dishes were
served, including a wide assortment of
green vegetables. The delectable quali-
ties of the greens were so distinctive
that I naturally paid the Ambassador a
special compliment on them. The Am-
bassador quickly made the point that the
green vegetables were all from Ghana. I
was somewhat embarassed because I be-
came distinctly aware of the lack of
imagination that has surrounded our use
of the vegetables that are readily avail-
able. I hasten to add that throughout my
travels in Africa and other parts of the
world, I have encountered a number of
plant species whose leaves are accepted
as edible. My plea is that a number of
these green-leafed plants may be high
protein sources, and therefore it is our
responsibility as research scientists to
investigate these plants for their nutri-
tional importance both for human food
and for animal feed.
In addition to the native plants that
should be reviewed for their possible
use, there are some important tropical
plants that can be introduced to Africa
which could assume the importance that,
for example, maize, rice, cassava and
groundnuts have achieved. The winged
bean (Psophocarpus tetragonolobus) is a
legume of far-eastern tropical origin with
tremendous nutritional possibilities. In
the recent report *‘Underexploited Trop-
ical Plants with Promising Economic
200
Value,’ it was described as follows:
‘‘The winged bean is a tropical legume
with a multitude of exceptionally large
nitrogen-fixing nodules. It produces
seeds, pods, and leaves (all edible by
humans and livestock) with unusually
high protein levels; tuberous roots with
exceptional amounts of protein; and an
edible seed oil.”’
The winged bean has important poten-
tial for small-scale farmers. It is a fast-
growing perennial that is particularly
valuable because it grows in the wet
tropics where protein deficiency in
human diets is not only great but difficult
to remedy. Winged bean seeds rival soya
beans (Glycine soja) in oil and protein
content, and the plant has the added
advantages of protein-rich roots and
edible foliage.
Though relatively unknown, this multi-
purpose legume appears to meet many
dietary needs of the tropics.
I can forsee this legume assuming the
same importance as soya beans in the
very near future. After all, it was only
fifty years ago that the soya bean became
a prominent Asian crop, especially in
China and Japan. Today, because of in-
tensive agronomic research on the soya
bean, it has become one of the principal
crop plants in the world. When I visited
Sri Lanka in June 1975 as a member of
the U. S. Academy of Science’s team
that participated in a workshop on
‘‘Natural Products for Sri Lanka’s
Future,’ I discovered that the tender
pods of the winged bean plant are
delicious and heavily consumed in that
country. The flowers, leaves, and shoots
are eaten as vegetables. The stem of the
plant serves as animal feed. Some vari-
eties of this plant produce a fleshy tuber
similar to the potato. It tastes very
much like potato, and it contains 20%
more protein. Its protein content is there-
fore 20 times that of cassava and certainly
10 times more than yams and other
edible root crops.
I am delighted to inform you that to
my knowledge the Agricultural Research
Station of the University of Ghana and
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
the International Institute of Tropical
Agriculture in Nigeria are already doing
some work on this highly promising plant.
In addition to looking for new crop
plants, it is essential that we do not
lose sight of the limited uses to which
we are currently putting the existing
crops that feature in our diets. For
example, a substantial portion of the
cassava harvest in Africa is eaten boiled,
roasted, or in the form of Gari. A certain
amount of bulk cassava is used in pre-
paring tapioca and starch. The potential
for world market uses for cassava
products is substantial. Apart from grow-
ing cassava for human consumption,
two major markets have not been ex-
ploited to the fullest. The industrial
starch market is still open. People often
forget that cassava starch has found
application in the manufacture of food-
stuffs, textiles, and adhesives for stamps
and envelopes, as well as newsprint,
cardboard, gelling agents, fillings and
munitions. The major markets for indus-
trial starch include Japan, the United
States and Canada. Because of the erratic
supply of cassava starch from many
developing countries (and this includes
those in South America) the developed
countries have been using only a small
percentage of cassava starch in their
manufacturing industries. If we can
prove to prospective buyers that we are
able to supply this needed raw material
on a sustained basis and at competitive
prices, I have no doubt that we can be
assured of handsome financial returns.
The other use for cassava requires
substantial quantities of pellets for the
animal feed market. Several European
countries are now using large quantities
of cassava as a cheap source of carbo-
hydrate for livestock. Many livestock
production concerns have realised that
it is relatively cheaper to prepare feed
from cassava and soya beans than to use
cereals. In fact it has been shown that
an equal mix of cassava and soya beans
is a feed superior to an equal mix of
soya beans and maize. To my knowledge,
Thailand is shipping large quantities of
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
cassava chips to Europe. Obviously,
because of our proximity to Europe and
because of the large amount of marginal
land available to grow cassava, the West
African countries can develop a sub-
stantial market for this product.
Several other plants of tropical origin
have been identified in the report on
‘‘Underexploited Tropical Plants of
Promising Economic Value.’’ I urge you
all to take a look at the report and make
use of as many of the recommended
plants as possible.
Plants Containing Special Qualities
The exploitation of our biological
resources should not be confined to only
those plants and animals that feature in
our daily diet. Some plants can indeed be
exploited in external markets for sorely
needed foreign exchange. In recent years
it became obvious that the cyclamates
used as a sweetening agent in a number
of baby foods as well as soft drinks have
some deleterious effects on man. It,
therefore, became necessary to seek a
sweetening substitute. After much exper-
imentation in the United States and
Europe, special interest was centered on
the Miracle Berry (Synsepalum dulcifi-
cum), a West African plant. The pulp of
its fruit obscures the sour taste of various
food substances. As I pointed out in an
earlier publication, Ghanian children
often show great delight in impressing
their friends that they can consume sour
fruits such as lemon, lime, and grapefruit
without expressing any distaste. This
plant soon became a subject of intensive
research in a number of American and
European laboratories. The amino acid
composition of the protein of this berry
was soon worked out. The active princi-
ple of the berry was found to be a glyco-
protein with a molecular weight of about
44,000. Soon after the labile glycoprotein
was Stabilized, and this enabled its use
in a pill form as a sweetening agent. I
must add that its use has not been con-
fined to sweetening ordinary foods and
drinks; it has also been used as a
sweetener for diabetics. Imaginative
201
individuals in America and in Europe
have taken advantage of the natural
chemical properties of the berry only to
enjoy vaginal secretions that change in
taste from sour to sweet as part of their
sexual amusement. The pills manufac-
tured from this plant are known as the
‘‘Miracle Fruit Drops.’ The Miracle
Berry plant is an economically important
biological resource that should be ex-
ploited further. The plant grows in the
wild in West Africa. It could easily be
brought into cultivation and the harvest
exported to pharmaceutical companies
that manufacture the pills.
Medicinal Plants
Historically, plant-derived drugs have
featured prominently in the treatment of
all kinds of disease in Africa. The admin-
istration of the drugs has been in the
hands of native herbalists. Plant species
have been variously used to arrest con-
vulsions, stop natural habitual abortions,
cure syphilis, suppress chronic ulcers,
remove warts on the sole of the foot,
de-worm the afflicted, arrest asthma,
serve aS mosquito repellent, induce the
flow of breast milk, etc. Over the years
I have accumulated information on the
uses of over 200 plant species from
Ghana alone. No doubt several impres-
sive lists could be obtained for other
African countries.
Throughout the world today there is a
serious shortage of supply of plant-
derived drugs. Several of the drug-
producing plants available in Africa can
be developed into the basis of a highly
sophisticated natural products industry.
Some of the plants could be cultivated
for the manfacture of end-product drugs
or processed to yield compounds that,
on chemical modification, can yield
additional drugs. In some cases extrac-
tions could be made for use as primary
Starting material for the synthesis of
several drugs. My own studies of yams
(Dioscorea sp.) over the years have
shown that the active principle diosgenin
is not a useful drug by itself, but it is a
starting material for the synthesis of most
of the oral contraceptives on the market
202
today. In recent years the plant Fagara
xanthoxyloides has become a very im-
portant material in the cancer research
programs in the United States. Other
plants such as Griffonia simplicifolia,
Fagara macrophylla and Rauwolfia
vomitoria are being collected from the
wild in large quantities for shipment
abroad. The financial possibilities are
endless. I will only remind you that, for
example, in 1974 the United States of
America produced great quantities of
drugs derived directly from plants and
sold them to the consumer to the tune
of three billion dollars. This figure does
not include the sales of antibiotics. I
wish to emphasize again that a carefully
planned screening program of the drug-
producing plants will yield fantastic
financial results for Africa.
Animal Protein Production
Throughout the history of Africa, the
utilization of wildlife as a major source
of meat protein has been significant.
However, traditional hunting practice
has led to a decrease in the populations
of some of the choice game meats. In
Ghana, for example, meat of the grass-
cutter (Thryonomys swinderianus) seems
to get more and more expensive in the
local open markets even if its availability
seems to be quite normal. In fact, it has
been observed that the more the supply
of the grasscutter meat in the city markets,
the higher the price. This observation
simply means that the supply of this
particular bushmeat is not meeting con-
sumer demand.
There are several species of game
animals that have proven to be good
protein sources. In East Africa game
animals such as the eland, impala, zebra,
wildebeest, giraffe, duiker, warthog,
steenbuck, waterbuck, buffalo, bush pig,
elephant and kudu feature daily in the
diets of many people. One of the game
reserves I am familiar with is the Mole
National Park in Ghana. The game ani-
mals I encountered there include harte-
beest, buffalo, waterbuck, roan antelope,
kob, bushbuck, oribi, duiker, warthog,
baboon, patas monkey and green mon-
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
key. All these animals constitute sub-
stantial sources of protein if their num-
bers are allowed to swell and then
cropped. Unfortunately, very few sys-
tematic attempts have been made to
establish game ranches in order to
maximize their production. From the
few studies that have compared cattle
and game animals, it is evident that the
production of game animals generally
outstrips that of cattle on all counts,
especially if we take into consideration
the marginal status of the available land
and the carrying capacities of the various
habitats for the two groups of animals.
It is now a well-known fact that the
effects of domesticated game animal
grazing pressure on natural vegetation
are less harmful than those of cattle
and certainly more favorable than those
of goats. Several detailed studies con-
ducted on game ranches in East and
South Africa have demonstrated that
game animals can be supported without
damage to grass cover and without any
serious destruction of the soil. On the
other hand, lands used for cattle ranching
are almost invariably rendered useless
because of the serious damage to the
soil and vegetation. Different species
of game animals graze and browse on
different plant species within a habitat.
Hence the presence of a variety of dif-
ferent game animals within one particular
vegetation-type should not give cause for
much concern. In a recent study con-
ducted in the Serengeti-Mara Game Re-
serves, it has been shown that the two
most abundant grazers in the reserves,
the wildebeest and the Thomson’s gazelle,
manage to co-exist instead of competing
for food. The wildebeest is a heavy
grazer, and as it migrates across the
Serengeti Plains it somehow stimulates
the growth of the plant species that
are exploited by the gazelle in the dry
season. This clearly shows a co-existence
between two heavy grazers which depend
upon the same habitat for their survival.
Another important factor to consider
is the fact that the total biomass of
game animals living on low quality land
is about equal the total biomass of cattle
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
on a much better quality land. Further-
more, and perhaps most important, is the
quality of protein produced by game
animals as against that produced by
cattle. Various studies on the nutritional
value of bushmeat have shown that the
quality of protein is at least as high as
that of cattle. In addition, the vitamin
content of bushmeat is much higher than
that of beef, mutton, or pork.
Another advantage in favour of game
animals, as a source of protein, is that
less food energy is needed to bring
their weight up before cropping. The
amount of grain used in feeding cattle,
sheep and pigs before they are slaughtered
is being questioned by energy conserva-
tion minded persons all over the world
today. It is, therefore, important that we
seriously consider the feeding require-
ments of the conventional domesticated
animals as against the natural feeding
habits of game animals.
There is no doubt that the demand for
bushmeat is increasing in many parts of
Africa. It is, therefore, necessary that
proper investments are made to infuse
sophisticated management into game
ranches so that those establishments
can be self-sustaining and yet produce
a greater quantity of protein.
As I intimated earlier, East and South
Africa have had more experience in game
ranching than has West Africa. In
Botswana, for example, a number of
game farms manage wildlife along with
cattle on a sustained-yield basis. The
Galana Game Ranch Research Project
in Kenya was started in 1970 to explore
the best methods for exploiting domes-
ticated game. One of the Project’s activi-
ties is the management of both game and
conventional livestock under identical
ranching conditions. In a screening pro-
gramme, game animals such as the
fringe-eared oryx, eland, buffalo, ostrich,
and the Peters’ race of Grant’s gazelle
have been herded with Boran cattle,
small East African goats and crossbred
Dorper, Masai, and Merino sheep. I
have no doubt that this project is going
to be successful in view of the quality of
203
the scientific manpower and institutions
involved in the entire programme.
I also have learned that a proposed
Nazinga Game Ranch Project for Upper
Volta is being planned at the moment by
the African Wildlife Husbandry Develop-
ment Association of Canada and various
agencies of the Upper Volta Govern-
ment. If this project becomes a reality
it will be the first well-planned game
ranching project for West Africa. The
practical information that will be derived
from the proposed project undoubtedly
will be of tremendous benefit to other
West African countries contemplating
similar projects.
In addition to bushmeat production,
properly managed industries can be
developed to handle the production of
processed animal skins and trophies for
sale. It seems logical that we can combine
game ranching and sport hunting in our
quest to seek substantial alternatives
for the biological resources of Africa.
Fish Protein Production
No discussion of the biological re-
sources of Africa can be complete
without careful consideration of the fish
fauna of the continent. We are all aware
that fish is abundantly rich in high quality
protein in addition to fat, minerals and
vitamins. It is well known also that the
nutritive value of fish is, in many cases,
superior to that of beef and that it also
is readily digestible and not easily
denatured by cooking. For centuries our
fishermen have exploited both marine
and fresh waters. Based on earlier
figures, I estimate that nearly 3.5 million
metric tons of fish are currently harvested
annually in Africa. Unfortunately, a sub-
stantial proportion of the catch is spoiled
because of the lack of refrigeration
facilities in most homes. Furthermore,
because of the fish preferences of our
people, several perfectly nutritious spe-
cies of fish are not eaten. It seems ob-
vious that with current techniques
available in Africa, many of the unpopu-
lar fish, as well as the large quantities of
204
perfectly desirable fish that are lost by
spoilage, can be used in preparing fish
protein concentrates for direct consump-
tion by humans as well as in the prepara-
tion of fish meal for cattle and poultry
feed:
In recent years a number of our coastal
countries have been engaging in deep-sea
fishing on a commercial basis. While on
a recent visit to Japan, I was gratified to
eat some prawns and shrimp that were
of West African origin. However, certain
foreign fishing fleets have been invading
the territorial waters of Africa to the
extent that if international agreements
are not concluded soon most of the choice
fish will be overexploited before Africa
is ready to embark on a full-scale fishing
industry.
In the case of fresh-water or inland
fishing practices, many changes are
necessary. In most cases, the fishing
techniques of the Neolithic have not
been improved upon. In areas where
fishing techniques have improved, very
little study has gone into the assessment
of the fish populations in rivers, lagoons
and lakes. As a result of our lack of
knowledge of the breeding systems of
the various species of fish in African
inland waters, certain fish populations are
being overly exploited. In a number of
cases we do not know the species com-
position of many of the inland waters on
the continent. I need not emphasize that
a number of the natural and man-made
lakes in Africa have tremendous potential
for the production of fish protein if
proper management principles are fol-
lowed. Most of us are familiar with the
importance of species of Tilapia in the
diet of many peoples of East and West
Africa. Unfortunately, our enthusiasm
for eating this delicious fish has not
been matched by our desire to study in
detail all aspects of the biology of this
fish, particularly its adaptation to pond
culture. It is essential that if we want
to derive maximum financial benefit from
our fish resources, we must encourage
systematic scientific research in all areas
of fish biology.
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Changing Food Habits
Seeking alternative biological resources
for food, especiaily for home consump-
tion, presupposes that the dietary habits
of our people are not static, but are
dynamic. Every society’s food habits
are governed to some extent by customs,
traditions, and cultural beliefs. In some
societies the taboos against certain food-
stuffs are so rigid that even in the case
of acute famine, the overly zealous would
rather die than eat “‘forbidden’’ foods.
Fortunately, most African societies are
more flexible and capable of practical
considerations in their eating habits than
some of their Asian counterparts.
As I have indicated earlier, most of
the major food items that feature con-
stantly in our diets have been introduced
into Africa. There are many Africans
who cannot even accept the fact that
plants such as cassava, corn, groundnuts
and rice are foreign foods. On the basis
of our past history, we already have the
propensity to adapt to new food items.
In 1968 a book entitled ‘‘Food Com-
position Table for Use in Africa,’’ was
published jointly by the United States
Department of Health, Education and
Welfare (HEW) and the Food and Agri-
culture Organization of the United Na-
tions (FAO). As its name implies, this
work contains information on the protein,
carbohydrate, mineral, vitamin and mois-
ture content and the food energy value
of many of the biological resources of
Africa. The nutritive value of many
plant and animal species has not been
studied as yet. Nevertheless, this book
is a good starting point from whence
we could begin to take a hard look at
the nutritive potential inherent in our
biological resources.
Many of the food items discussed in the
book are already being utilized in various
sections of our societies. What is needed
is the popularization of many of the foods
not being utilized by introducing them
into the commercial markets.
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Summary
It is interesting to note that of the
continents composed of developing coun-
tries, Africa is certainly the one in which
most is known of its flora and fauna. The
plant resources of Africa are certainly
better known than those of South Amer-
ica. What is lacking is a rational asess-
ment and utilization of the botanical
resources of Africa. This is equally true
of the level of our knowledge of the
major faunal elements. Much work is
needed to improve our knowledge of the
biology of the small mammals and the
lower plants.
Be that as it may, a number of our
scientists (both pure and applied) and
their administrative superiors are not
even aware of the magnitude of and the
potential inherent in our biological
resources. [t seems obvious that for
African governments to obtain maximum
utility from their biological resources,
a concerted effort should be made to
review the existing structures of scien-
tific and technical organisations and to
intensively review the native flora and
fauna, so that their facility for solving
problems and applying imaginative think-
ing to their research efforts can be
realised to the fullest extent.
Bibliography
Ayensu, Edward S. 1972. Morphology and Anatomy
of Synsepalum dulcificum (Sapotaceae). Bot.
Jour. Linn. Soc. 65(2): 179-187.
. 1975. Science and Technology in Black
Africa, pp. 306-317. In World Encyclopedia
of Black Peoples, Vol. 1. Scholarly Press, Inc.
St. Clair Shores, Michigan.
Dasmann, Raymond F. 1964. African Game Ranch-
ing. Pergamon Press. London.
National Academy of Sciences. 1975. The Winged
Bean—A High-Protein Crop for the Tropics.
National Research Council, Washington, D. C.
. 1976. Underexploited Tropical Plants of
Promising Economic Value. National Research
Council, Washington, D. C.
Purseglove, John W. 1972. Tropical Crops, Vol. 1
and 2. Wiley Inter-Science, New York.
United States Department of Health, Education and
Welfare and Food and Agriculture Organization
of the United Nations. 1968. Food Composition
Table for Use in Africa. Maryland and Rome.
205
PROFILE
A Polish Naturalist in Peru:
The Life and Work of Felix Woytkowski
Ashley B. Gurney
Collaborating Scientist, Systematic Entomology Laboratory, IIBII, ARS, USDA.
Mail address: clo U. S. National Museum, Washington, D. C. 20560.
Museums of natural history throughout
the world are filled with specimens of
animals and plants which bear labels
telling where they originated, and when
and by whom they were collected. Other
label information may explain field con-
ditions, abundance, and local importance
where found. The names on labels of
collecting localities and of collectors are
necessary for adequate documentation
and may be of much special importance
if it is desired to revisit the locale for
more material or to clarify some obscure
aspects of the original collection. Apart
from practical considerations, however,
the student, whether expert or novice,
using preserved specimens often develops
a personal interest in a collector, whom
at first he may know only as a name on
labels. If those of us handling specimens
do not Know the collector’s background,
we often wonder what kind of person he
was and whether his label data reflect
accurate observations. Why did he de-
vote time to such a pursuit in those
perhaps long-past years? What were his
life-style, his aspirations, and the nature
of his family?
In future years, many scientists may
wonder about Felix Woytkowski, whose
name appears on the labels of thousands
of insects and plants which he collected
in Peru during 1929-64. This large body
206
of material, located in numerous museums
in the U. S. and elsewhere, is of so much
importance, and Woytkowski’s life was
of such dedication to energetic collecting
and the accumulation of accurate field
data, that a short review of his career
is timely because of an extensive recent
biography (1, 2).
In 1929, at the age of 37, Felix Woyt-
kowski arrived in Peru with his wife and
4-year old son; he left in broken health
in 1965 to return to Poland, where he
died in April 1966. For most of 35
years he actively studied the plant and
insect life of Peru, chiefly as a collector
who took pride in gathering specimens
for leading professional botanists and
entomologists who benefited from the
carefully recorded information which
accompanied the material. He travelled
throughout most of Peru (his expedition
itineraries list 16 Departments in which
he collected) and noted the altitudes
and zonal regions in which the various
species occurred. Much of the country
had never been examined with equal
thoroughness by earlier collectors, so
hundreds of species were new to science,
and the information gathered about
plants and insects as a whole was tremen-
dous. Naturally, not all of the specimens
added to museums or the data already
published in basic descriptive papers
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
have yet been synthesized in final form
for biologists. In addition to collecting
museum specimens, which he sometimes
did on a part-time basis, he was asso-
ciated for several years with San Marcos
University in Lima, especially with the
Botanical Garden there. Also, for 7 years
he was employed by the Swiss firm,
CIBA, in the search for plants of medici-
nal value. Thus, we see that Woyt-
kowski’s life was one of solid achieve-
ment on the frontier of science in the
natural history studies of his adopted
country.
Though for years Woytkowski con-
templated writing a book about his work
in Peru, was encouraged by many
friends to do so, and took 3 chests of
records (in Spanish and English) when
he returned to Poland, he did not live to
sort out the material. Later, his niece,
Dr. M. Salomea Wielopolska, arranged
and translated much of the material into
Polish and assembled the manuscript of
this book which, together with other
information, is the basis for my brief
biographical account. She then donated
the Woytkowski records to the Polish
Academy of Sciences in Warsaw (3).
Felix Woytkowski was born May 20,
1892 at Grzymaloéw in eastern Galicia,
near the Zbrucz River which at that time
was the boundary between Russia and
Austria. In Poland of Pre-World War I,
the Woytkowski family was one of com-
fortable financial position and social
Standing. Felix’s father was a physician
with a large practice who _ habitually
treated those who were poor on a “‘gratis’’
basis, and Felix’s grandfather had a large
farm which included cultivated fruit
trees from abroad, a botanical garden
and heated greenhouses. In fact, the
family had owned several estates and
there was a tradition of pursuing agricul-
ture and horticulture on a scientific
basis. With this sort of background,
Felix began when 12 years old, together
with his brother Tadeuza, to collect
insects and plants. An experienced
botanist gave them guidance, and they
made a large herbarium collection from
local wooded hills which later was pre-
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Fig. 1.—Felix Woytkowski at about 35.
sented to the University of Lemberg
(Lwow). The family could afford visits
to other European countries, and the
boys grew up familiar with libraries
and museums, and they had an apprecia-
tion of cultural and scientific values.
Felix enjoyed music, painting, and
literature, and the latter had a deep
influence on him. This influence, as well
as his command of the English language,
is shown by sentiments later expressed
in various letters and notes relative to
his rich and varied experiences in Peru,
for instance a paragraph quoted by Good-
speed (4): ‘‘The Andean heights, their
utter wildness, their vast and _ silent
alpine plateaus, their sheer descents
into the Amazonian jungle, their moun-
tain folk and the malignant spirits which
for them haunt the high altitudes, create
something which ever beckons anew.
Within them there are glorious moments
to live; there the air is freer and strangely
inspiring; there one can learn some of the
207
Fig. 2.—Felix Woytkowski after returning to
Poland.
elsewhere forgotten lore of ancient
peoples; there plants and animals as well
as air, sky and thoughts differ from
anything we know here below. There we
learn to conquer fear and suffering and
satisfy our scientific curiosity in a vast
kingdom of alluring adventure.’’
After completing secondary school in
Lwow in 1911, Felix spent a year at
Liege, Belgium at the “Ecole des Hautes
Etudes de Sciences Commerciales et
Consulaires.’’ Later, he studied at Ox-
ford University, England, where he took
economics and political sciences pri-
marily, though he had a tutor to help
perfect his English. With the outbreak
of World War I, money from his parents
was discontinued and he secured work
in several grammar schools as a teacher
of chemistry, Latin, Greek and other
subjects. At Huddersfield he was a textile
worker for a while and he became in-
terested in the new ideas of Sir Sidney
Webb concerning trade-unionism.
In 1918 a Polish army was organized
in France by the Pole, General Joseph
Heller, and Felix went there and en-
listed as a volunteer, being assigned to
the General’s staff as an interpreter
with the rank of Second Lieutenant.
After the war he returned to Poland,
where he first worked as the secretary
of the Mayor of Warsaw. Later, in
Graudenz, he was the foreign corre-
spondent for the largest Polish foundry
208
and enamel works. In 1923 he turned to
agriculture and worked as an apprentice
on 2 large estates. The war and the
ensuing inflation created upset and im-
poverished conditions which, after he
married and had the welfare of a wife
and son to think of, led him to consider
going abroad, first to Canada. However,
he decided on Peru.
Felix and his family joined a group of
Polish emigrants who arrived in Lima
June 26, 1929, but he soon left the group
in favor of aGerman colony at Villa Rica,
Province of Tarma. Relating his experi-
ences to C. P. Alexander in 1944, he
wrote of soon finding it more difficult to
make a living in Peru than in Europe.
He also was attracted to the wooded
surroundings and opportunities for natu-
ral history studies, then largely neglected
in Peru. Woytkowski was a close friend
of Pedro Paprzycki, another Pole who
collected insects in Peru. After con-
tacting specialists in the U. S., he found
a ready market for specimens and for
many years some of the same ento-
mologists and botanists continued to
receive material from him. Dr. Alexan-
der, the veteran student of crane flies,
H. B. Hungerford (Hemiptera), J. D.
Hood (thrips), Leonora Gloyd (dragon-
flies), and F. M. Brown (butterflies)
were among the entomologists who
regularly received much useful material
from him. T. H. Goodspeed (tobacco
relatives and other plants), Charles
Schweinfurth (orchids), and J. F. Mac-
bride (Flora of Peru) were among the
botanists for whom he worked especially.
Through John D. Dwyer, a large collec-
tion of plants was acquired by the Mis-
sour! Botanical Garden, St. Louis,
Missouri (5).
The itineraries of collecting trips
presented in chart form on pp. 289-298
of the book are arranged by years and
show altitude, the type of terrain, also
the Province and Department of each
locality where collecting occurred. Six
folding maps held looseleaf inside the
back cover show collecting localities,
other place names and various routes
traveled. The charts also indicate the
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
chief periods of involvement at the
Botanical Garden and with CIBA.
Throughout Woytkowski’s book there
are frequent references to Callanga, a
Peruvian locality apparently first brought
to his attention by Professor Hungerford
who in 1929 had described an interesting
new species of water-strider, Velia
helenae, from there (6). A single female
specimen of it, labelled ‘‘Callanga,
Peru,’’ without data or collector’s name,
had been found in the Riksmuseum,
Stockholm, Sweden. Many insect speci-
mens similarly labeled occur in several
European and U. S. museums, and the
abundance of unnamed species among
them gave the impression of rich ende-
micity. Woytkowski has written that as
early as 1935 he thought of going to
Callanga to get more of the Velia as well
as other hoped-for rarities, but he had
difficulty in clarifying its exact location
and in accumulating adequate funds to
support the effort. Finally, after periods
of great enthusiasm for doing so, as well
as discouragement, he carried out ex-
plorations to Cuzco and nearby areas of
southeastern Peru in 1951—53, including
an early 1953 visit to Callanga, in
southern Madre de Dios. He described
going there, far down into a deep valley
surrounded by steep hillsides, but he did
not find Velia helenae and was much
disappointed (7). There was some un-
certainty whether the name Callanga
represented a village or a river of the
same name, and as a whole he felt
that his Callanga trip was a failure (8).
It is sad to report that in spite of Woyt-
kowski’s skill as a collector he often
was barely able by this occupation to
support his family and his collecting
trips, frequently away from home for
many weeks. During 1946-55, when I
purchased insect specimens from him, his
letters often told of the urgent need for
funds. On June 10, 1951 he wrote me of
working a year in northwestern Peru for
a petroleum company in order to finance
a trip to southern Peru, ‘‘toiling daily
within this vast corporation and living in
the company’s camp upon the barren
desert of the tropical Pacific coast, so
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
far north and so far from the Peruvian
capital Lima.’’ Later, near the end of his
Peruvian work when afflicted by failing
health, including angina pectoris , he was
forced to sell his camera and equipment
and was assisted by loyal friends in ob-
taining funds for the return to Poland.
He had been divorced earlier, his only
son George had died in 1952, and a
grandson and two granddaughters ap-
parently remained in Peru.
During Felix Woytkowski’s life, warm
appreciation for his work was expressed
by various scientists (4, 9).Yet, in his
final period of poor health and financial
difficulty he may have wondered if his
somewhat lonely life in Peru had been
worthwhile. For many naturalists whose
main work has been the collecting of
specimens in places far from their
original homes, life has brought relative
obscurity, a precarious livelihood, dan-
gers, sickness, and sometimes crushing
disappointment when large collections
were lost by shipwreck or deterioration
from weather. Of course, it is different
only in kind from the frustrations of
innumerable human lives. In the case of
Woytkowski, we have the published
record of a very talented and dedicated
naturalist, and he has left thousands of
well preserved and carefully documented
specimens which continue to enlarge the
scientific studies of numerous other
workers, improving the basic knowledge
of South America. He will not be for-
gotten.
References and Notes
1. Peru-moja ziemia niebiecana (Peru-my un-
promised land). 1974. by Felix Woytkowski.
Translated into Polish and arranged by
M. Salomea Wielopolska. 304 pp., 105
photos, 6 separate folded maps. Ossolineum
(publisher), Wroclaw. Polish distributor: ARS
Polona, Warsaw, Krakowskie Przedmiescie 7,
Poland. Available in U. S. from International
University Booksellers, 101 Fifth Ave., New
York, N. Y. 10003. Paperback, $16.25. (The
book may be translated into English.)
2. For generous assistance during the preparation
of this biographical review I am indebted to
numerous persons. George W. Byers and Peter
D. Ashlock (University of Kansas) advised me
about Woytkowski specimens obtained by
209
Dr. Hungerford. C. P. Alexander (Amherst,
Massachusetts) opened up a large amount of
information based on his long-term corre-
spondence and put me in touch with Maria
Salomea Wielopolska, who sent a copy of the
book and enthusiastically answered numerous
detailed questions. The Polish Academy of
Sciences kindly furnished photographs. Several
local friends and colleagues have been helpful,
particularly Eugene Jarosewich (Mineral Sci-
ences, U. S. National Museum of Natural
History) and my neighbors Frank and Gene
Gonet, who translated paragraphs of Polish for
me. John J. Wurdack (Botany, U.S.N.M.N.H.)
has been especially helpful with references to
Woytkowski’s botanical work. Finally, Gerardo
Lamas of Lima, Peru, a visiting entomologist,
gave me a clearer insight into Woytkowski’s
collecting localities.
. Dr. Wielopolska, now retired and occupied
with writing tasks, was for 25 years the Chief
Librarian at the Technical University in
Szczecin. She has always been interested in
natural history and early began the serious
study of forestry, which, however, was in-
terrupted by World War II, after which she
pursued a career in liberal arts and library
science.
. Goodspeed, T. H. Plant Hunters in the Andes
(2nd Ed.) 378 pp., Univ. of California Press
(1961).
. Dwyer, J. D. A preliminary report on Woyt-
kowski’s last Peruvian collection. Phytologia,
vol. 15: 458-461 (1968); La coleccion de
plantas peruanas de Felix Woytkowski en el
Missouri Botanical Garden (1958-1962). Ray-
mondiana, vol. 4: 5—71 (1971). (The second
paper is nearly identical to the first one
except that a large list of plants, some 2,000
species in number, is included).
. Hungerford, H. B. A new Velia from Peru
(Homoptera, Veliidae). Entomol. Tidskrift
(Stockholm), vol. 50: 146-147 (1929).
7. Additional Peruvian specimens of helenae
have since been reported from the Department
of Junin. Polhemus, J. T. A new Velia from
Peru, and the description of the male of Velia
helenae Hungerford. Proc. Entomol. Soc.
Washington, vol. 71: 55—S9 (1969).
. One of the folding maps accompanying the
book was prepared by Prof. Hungerford to
show the supposed location of Callanga, and
it probably was based on data sent to him
by Woytkowski. The map was sent to
Woytkowski with a letter dated March 31, 1953.
after the expedition was completed, but neither
of them was certain of the significance of
‘*Callanga.’’ From Gerardo Lamas of Lima I
have now learned that Callanga was a hacienda
which was visited much earlier by one or
more individual collectors, chiefly Gustav
Garlepp (1862-1907), a German who made
4 South American trips between 1883 and 1907,
when he died in Paraguay by a ‘“‘treacherous
murder.’’ Garlepp, sometimes aided by his
brother Otto, collected actively and specimens
were distributed widely, mainly through the
firm of Staudinger and Bang-Haas of Dresden.
He probably was in Callanga about 1890.
Accounts of the Garlepps were written by
Niethammer (Bonner Zoologische Beitrage,
vol. 4: 195-303, 1953) and Papavero (Essays
on the History of Neotropical Dipterology,
vol. 2: 293-295, 1973). Callanga was destroyed
by Indians in this century, perhaps about 1940,
according to Dr. Lamas’ information, and at
the time of Woytkowski’s visit remnants of
the single hacienda (farm) were all that
remained. It was located at about 12.59 S. Lat.,
71.13 W. Long., at an altitude of about
1500 m. Some collections from ‘‘Callanga”’
may have been taken at different elevations
in the neighborhood of the hacienda.
. Soukup, J. Felix Woytkowski, veinticinco
anos dedicados a biologia. Biota, vol. 1:
30-33, 1 fig. (1954); Felix Woytkowski
(1892-1966). Biota, vol. 6: 150-153, 1 fig.
(1966).
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
RESEARCH REPORTS
A New Species of Platycystites (Echinodermata:
Paracrinoidea) From the Middle Ordovician of Oklahoma
T. J. Frest, H. L. Strimple, and M. R. McGinnis
The first two authors are affiliated with the Department of Geology, University of
Iowa, Iowa City 52242; the last-named with the Department of Bacteriology &
Immunology, University of North Carolina, Chapel Hill 27514.
ABSTRACT
The paracrinoid Platycystites infundus, new species, from the Bromide Formation
(Middle Ordovician) of Oklahoma provides additional evidence that at least some
paracrinoids lay upon the substrate or partially embedded on it. The inferred mode of
life, based on stem attachment and thecal morphology, of the 3 species now ascribed to
Platycystites suggests that only 1 (P. faberi Miller) was held erect above the sea bottom
by its column.
The rare paracrinoid genus Platycys-
tites (Order Platycystitida Parsley and
Mintz, 1975) is presently known only
from southwest Virgina, northeast Ten-
nessee, and southern Oklahoma. Like
most other paracrinoids it is restricted
to rocks of Middle Ordovician (Black-
riverian) age. P. faberi, type species of
the genus, was inadequately described
and illustrated by Miller (1889), who also
presented incorrect occurrence data for
the species. No further species were
added to the genus until Bassler (1943)
proposed several new species (P. bromi-
densis, P. cristatus, P. fimbriatus, P.
levatus), all from the Bromide Formation
(?Chazyan-Blackriverian) of Oklahoma.
Another Bromide species (P. bassleri)
was added by Sinclair (1945).
Though the distinctness of the genera
now grouped in the Paracrinoidea had
long been recognized, the group was
not raised to class status until 1945
(Regnell, 1945). By far the most com-
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
prehensive treatment of the paracrinoids
is that of Parsley and Mintz (1975). In
their paper they redescribed and reillus-
trated P. faberi and reduced all of the
Bromide species into synonymy with
P. cristatus Bassler. Apparently all of
the Bromide specimens studied by Bassler
and Parsley and Mintz came from the
lower echinoderm zone (informally desig-
nated the ‘‘Platycystites zone’’) of the
Mountain Lake Member, in which Platy-
cystites is prolific. The total thickness of
the beds through which P. cristatus
ranges is about 65 ft, but all are from the
lower part of the Mountain Lake (Parsley
and Mintz, 1975: 74). The single speci-
men described herein as Platycystites in-
fundus, n. sp., was collected by McGin-
nis from an exposure of the upper echino-
derm zone (of Fay and Graffham, 1969:
37-42) which occurs at the top of the
Mountain Lake, considerably above the
‘*Platycystites zone.’’ The echinoderm
fauna of this unit (informally termed the
211
Figs. 1-6.— Plate diagrams of Platycystites. 1, 2, Anterior and posterior views of P. cristatus (modified
from Parsley and Mintz, 1975, text-fig. 3); 3-6, anterior, posterior, left, and right views of holotype of
P. infundus. A-anterior plates; AB anterior basal; L, left plates; P, posterior plates; PB, posterior basal;
R, right plates; RB, right basal. Periproct black; positions of gonopore and hydropore indicated by
light lines.
212 J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
‘‘Oklahomacystis zone’’) differs con-
siderably from that lower in the Mountain
Lake. The paracrinoid genera Okla-
homacystis and Sinclairocystis have not
been found outside the zone and appear
to be endemic to this unit. A single
specimen of Platycystites has been col-
lected from the Oklahomacystis zone at
a locality near Sulphur, Oklahoma; the
specimen lacks the arms and stem but
it is preserved as well as are most para-
crinoids. This part of the Bromide is
not well exposed and the source exposure
is no longer collectible: J. Sprinkle
(pers. comm., 1976) reports that around
45 specimens, possibly referable to P.
faberi, have been collected from this
zone in the western Arburckle Mts.
(Oklahoma). None of these apparently
are referable to either P. cristatus or
P. infundus, n. sp.; hence it is unlikely
that any additional specimens of P. in-
fundus will be discovered in the near
future. Despite its imperfections, the
specimen preserves most important mor-
phological features and is clearly a dis-
tinct species.
The addition of a third species to
Platycystites necessitates some reevalua-
tion of the functional morphology of the
genus. In particular the thecal shape
and position of the stem facet of P.
infundus, n. sp., support the contention
of Durham (in Parsley and Mintz, p. 69,
figure 6) that at least some species of
this genus were recumbent upon or partly
buried in the substrate with the stem
acting as an anchor or as a tether rather
than serving to elevate the theca above
the sea bottom as Parsley and Mintz
(op. cit.) envision it. Nevertheless, we
have used Parsley and Mintz’s descrip-
tive terminology and orientations which
are partly predicated on the assumption
that their reconstruction of the living
position of Platycystites is correct. The
system they employ facilitates homolo-
gous comparisons between the genus and
other paracrinoids, particularly within
the Platycystitida. It can be applied with
little modification to P. infundus. Its use
does not, however, imply acceptance of
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
their interpretation of the genus’ mode of
life.
Higher classification of many of the
poorly known fossil echinoderm classes
is currently in a state of flux. As regards
the Paracrinoidea we have followed the
taxonomy of Parsley and Mintz through
the ordinal and class levels but refrain
from assignment of the class to a sub-
phylum. Parsley and Mintz (1975: 5-7,
25—26) erected the subphylum Paracrino-
zoa, with the single class Paracrinoidea,
for this distinctive group of echinoderms
because, according to these authors, the
paracrinoids cannot be placed in either
the Crinozoa (Matsumoto, 1929) or
Blastozoa (Sprinkle, 1973). Briefly the
justification for this action is that the
Paracrinoidea “‘have characteristics that
fit into both subphyla mentioned above
and they also have traits which are
peculiar to their own subphylum, e.g.
internally opening transutural slits, left
lateral offset peristome relative to the
column, along with a pronounced plate
increase in the right lateral margin and
bilateral symmetry defined by the G
plane’ (op. cit., p. 26). While these
characters collectively discriminate the
Paracrinoidea from other echinoderm
classes, none of them individually are
unique to it. Some features of the para-
crinoid thecal plate pore system are
strikingly reminiscent of those of eocri-
noids; more detailed analysis of it is
required to establish its uniqueness,
particularly since one order of Para-
crinoidea (Platycystitida) totally lacks a
pore system. Bilateral symmetry defined
by the G plane is also developed in some
Rhombifera (e.g. Pseudocrinites; see
Paul, 1967 and Kesling, 1968 for dis-
cussion). Lateral offset of the peristome
also occurs in other groups; examples
include Columbocystis (uncertain affini-
ties) and the diploporid cystoid Allocy-
stites (Parsley, 1975: 356-357).
The validity of the subphylum Blasto-
zoa Sprinkle has recently been ques-
tioned by Breimer and Ubaghs (1974a),
and Breimer and Macurda (1972) and
Macurda (1973) have presented mor-
213
phologic data indicating the presence
of tube feet in the Blastoidea, contra
Sprinkle. Without attempting to evaluate
the merits of the various points raised
by these authors, it is fair to say that a
consensus has not yet emerged. The
basic data required to establish which
characters are of importance at the
highest levels of echinoderm taxonomy
are still largely lacking. While quite
recently major essentially solid taxonomic
contributions such as those of Parsley
and Mintz (1975) and Sprinkle (1973)
have greatly clarified the status of a
number of puzzling fossil echinoderms,
it seems reasonable to expect that the
current information explosion in the
study of primitive echinoderms will con-
tinue for some time. Consequently we
feel that large scale rearrangements of
the echinoderm clases and, particularly,
a proliferation of subphyla are prema-
ture. We follow Parsley and Mintz (1975)
and Breimer and Ubaghs (1974b) in re-
moving the Paracrinoidea from the
Crinozoa, but like the latter authors do
not place it in a subphylum. We admit
the strong possibility that the Para-
crinozoa of Parsley and Mintz may even-
tually prove fully acceptable to most
workers.
Systematic Description
Class PARACRINOIDEA
Regnell, 1945
Order PLATYCYSTITIDA
Parsley and Mintz, 1975
Diagnosis. —‘‘Paracrinoids without sutural
pores; arms epithecal, typically branched; thecal
plates generally smooth with pustulose prosopon”’
(Parsley and Mintz, 1975: 57).
Family PLATYCYSTITIDAE
Parsley and Mintz, 1975
Diagnosis. —Theca ovoid to amygdaloid in
shape with approximately 27 plates identifiable
in juveniles, plus a variable number of intercalates
along the right side (some are generally present).
Arms 2, transverse, primarily epithecal (adopted
from Parsley and Mintz, 1975: 58).
214
Genus PLATYCYSTITES Miller, 1889
1889. Platycystites Miller, North American Geol-
ogy and Paleontology, p. 272.
Platycystis Miller, Bather, in Lankester
(ed.) Treatise on Zoology. III, Echino-
derma, p. 51.
Platycystis Miller, Kirk, U. S. Nat. Mus.
Proc. 41: 19.
Platycystites Miller, Bather, Roy. Soc.
Edinburgh, Trans. 49 (pt. 2) (6): 371.
Anomalocystites Hall, Springer, in Zittel-
Eastman, Textbook of Paleontology,
vol, lps 150:
Platycystites Miller, Bassler, Amer. Jour.
Sci. 241: 669-697.
Platycystites Miller, Regnéll, Lunds Geol.
Min. Inst., Medd., No. 188, p. 39.
Platycystites Miller, Sinclair, Amer. Mid-
land Nat. 34(3): 707.
Platycystites Miller, Kesling, Treatise on
Invertebrate Paleontology Part 5. (Echino-
dermata 3) 1: 288.
1975. Platycystites Miller, Parsley and Mintz,
Bull. Amer. Pal. 68(288): 59.
1900.
19 e
Wise
SS:
1943.
1945.
1945.
1968.
Diagnosis. —Theca amygdaloidal, compressed
to broadly oval and inflated in cross section, with
27 to 29 identifiable plates; some species with
additional intercalates along right lateral margin;
maximum number of plates about 47. Peristome
usually only slightly offset to left, periproct on
posterior face near upper margin. Arms 2,
epithecal, extending varying distances along the
lateral margins (modified from Parsley and Mintz,
p. 59).
Type species.—FPlatycystites faberi
Miller, 1889.
Range.—Middle Ordovician (Black-
riverian); Bromide Formation, Okla-
homa; Ottosee-Benbolt, Virginia and
Tennessee.
Remarks.—Our generic diagnosis dif-
fers only slightly from that of Parsley
and Mintz; the main difference is that
we do not recognize the presence of
intercalates in the type species. Our
interpretation of thecal plating in P.
faberi will be presented in a forthcoming
paper. For convenience the theca is
oriented in the plate diagrams with the
periproct uppermost and the stem roughly
opposite the periproct defining a vertical
longitudinal axis. This orientation is not
identical, in the opinion of the authors,
to that of the whole animal in life position
except possibly in P. faberi. Thecal
plate nomenclature and face terminologies
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Figs. 7-11.—Holotype of Platycystites infundus, n. sp.; 7-10, views of right, left, posterior, anterior
sides, all magnified x2.7 (9 and 10 are side views in presumed life orientation); 11, top view, centered on
peristome in presumed life orientation, x4.0.
are those of Parsley and Mintz as sum-
marized in their text-figure 3 (ibid, p. 60;
compare the explanation of our figs. 1—6)
except in minor details. The terms right
and left are defined relative to the
posterior face when the theca is viewed
in anterior-posterior profile as in fig. 2
and 4.
Platycystites infundus, n. sp.
Figures 3-11
Diagnosis.—Theca with about 33 plates, few
intercalates, not strongly inflated. Arm calluses
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
prominently developed, left arm nearly reaching
column. Theca strongly asymmetric, right side
flattened. Stem facet directed toward right.
Material. —One specimen, holotype SUI 39513,
from the ‘‘Oklahomacystis zone,’ top of the
Bromide Formation, Mountain Lake Member,
1.8 mi. Sulphur, Oklahoma.
Description. —Theca unevenly rounded in an-
terior-posterior profile; largest dimensions subequal,
length of holotype 22.0 mm; maximum width of
holotype 21.7 mm. Total number of thecal plates
about 33; few of these are intercalates (3 on
holotype). Theca flattened along right side, evenly
oval in outline when viewed along a plane normal
215
to axis through gonopore and hydropore and
center of right side (fig. 11). Stem facet elliptical,
not crenulate, narrow, width 2.1 x 2.0mm, oriented
parallel to proximal distal axis. Lumen small,
round, diameter 0.7 mm.
Basals 3, unequal; PB and AB large, equal in
area, developed on posterior and anterior faces
and left margin of theca. RB short, much smaller
in area than PB or AB, making up less than
one-third of column attachment facet. Left plates
3: L1 and L2 crossing thecal margin; L1 situated
immediately above PB and AB, hexagonal, crossed
transversely by left arm, developed more on an-
terior face; L2 above L1, 6-sided, arm callus
traversing the plate along its long axis, most of
plate area on posterior side. L3 to left of other left
plates, pentagonal, wholly on anterior face.
The 10 anterior plates plus the left plates make
up most of the anterior thecal face (figs. 3 and 9).
Subcentral on the anterior face is the large A2,
bordered by 8 plates. Immediately beneath A2 is
Al, a heptagonal plate that frequently is the
largest anterior thecal element in P. cristatus
(Parsley and Mintz, p. 62) but in this species is
considerably smaller than A2. A6 and A7, sub-
equal in area, border A2 on the left; A6 is nearly
equally 5-sided; A7 is irregularly hexagonal.
Most of the left anterior border is made up of
3 small plates (A10, All, A8—9) which do not
extend more than half way around the left side
of the theca. Al0 and All are small and un-
equally pentagonal; the single plate presumed to
represent A8 and AQ in P. cristatus (fig. 1) is
heptagonal and adjoins All and RB laterally
along the lower left anterior margin. Adoral to
A10 is R4, a small hexagonal element visible
on both sides of the theca and bisected by the
right arm seat which terminates on this plate
(figs. 6 and 7). No plate corresponding to R5 of
P. cristatus is present on the holotype of P.
infundus. R2, plus anteriors A3, A4, and AS fill
out the upper margin of the anterior face. These
plates are quite small in P. cristatus; they are
larger in area in this species, presumably because
of the more extensively protruded arm tracks.
A2 and A3 are pentagonal; their upper edges
terminate on the anterior face, as does that of
the small 4-sided A4. A5 is equally developed on
both faces; this plate forms the northwest quadrant
of the periproct border on the posterior face.
The periproct, located near the upper margin on
the posterior face, is surrounded by 4 plates,
each of which subtends an equal area of its border.
The right half of the periproct border is formed
by R3, which is bipartite; A5 and PS also con-
tribute to the periproct border. The periproct
opening itself is raised slightly and circular
(diameter 2.2 mm). A presumed hydropore is
located at the junction of PS, P6, and P7; the
opening itself cannot be seen, but it is likely
situated on the small raised triangular platform
visible where these 3 plates meet (figs. 4, 10). A
small round pore (gonopore), central on a raised
216
tubercle, occurs on P7. All plates along the upper
margin of the posterior face are elongated parallel
to the thecal margin. Between R3 and PB the
right posterior margin is made up of R4 and 3
small intercalates. Distal to P7 the left posterior
margin is defined by L2, L1, and PB. L2 passes
over onto the anterior face but is mostly posterior
in position. The central area of the face is occupied
by relatively few, large plates, i.e., PI—P5 and
P8-9. P1, the largest posterior plate, and P4 are
hexagonal; the pentagonal P2 and P3 are subordinate
in size to Pl and P8—9 in this species (compare
P. cristatus, fig. 2). The elongate irregular shape
of P8—9 is unusual; this plate may be abnormal
in this specimen and more usually 2 discrete
elements may be present as in P. cristatus.
Calluses for the epithecal arms are narrow
(average width 1.1 mm) but prominently extended
out from the theca throughout their length (figs.
9-11). The left arm extends around the theca
to about the midheight of PB before becoming
exothecal or terminating. The right arm callus
does not extend below R4. None of the arm
plates themselves are retained. The proximal part
of the left arm callus, and nearly all of the right
arm, is invaginated into the theca, forming a
trough. Proximal to the oral opening the troughs
appear to penetrate the bottom of the callus,
which is thus open to the interior. The thecal
plates, except in the areas making up the arm
calluses, are covered with a fine pustulose
prosopon. The column is unknown.
Derivation of name.—The specific
epithet refers to the presumed life
habit of the species (infundus, laid out
upon, spread on).
Remarks.—Platycystites infundus, Nn.
sp., differs from P. cristatus in a number
of ways as noted above; but given the
limited material on which P. infundus is
based and the small number of described
Platycystites species, the value of many
of the noted features of the holotype as
taxobases on the specific level is uncer-
tain. Only P. cristatus is known from a
reasonably large number of specimens
and has been described at length. A
definitive plate diagram of P. faberi,
together with detailed descriptions of
thecal plate identities and locations based
on a large series of specimens, would
facilitate platycystitid taxonomy but such
a series in unlikely to be available in
the near future. In their absence the fol-
lowing discussion is based primarily on
P. cristatus.
Some degree of variation in thecal plate
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
number has been noted by Parsley and
Mintz (ibid., p. 73) in P. cristatus; most
variable is the number of intercalates,
which can range between 2 and 17 in this
species. The other thecal plates are less
variable; their number is largely inde-
pendent of thecal size (height), they are
in more or less fixed position, and, though
their outline may vary, they are readily
identifiable from specimen to specimen
(ibid., p. 60). It is hence possible that
many of the deviations from P. cristatus
noted in the description of P. infundus
(e.g. bipartite R3, combined A8-—9 and
P8-—9, R5 missing or combined with
R4) may be significant at the specific
level. On the other hand, some of these
variations could also occur on an ab-
normal specimen, but when combined
with other noted differences they may
be utilized with more confidence. Pos-
sibly some of these features are related
to life habit. Paired small plates (i.e.,
Al10 and All, A8 and A9, P8 and P9 in
P. cristatus) may have originated through
bisection of what was originally a single
element. Replacement of a single plate
(normal condition for the population) by
2 elements in some individuals is known
in some Rhombifera: Paul (1966, 1968)
figures 2 examples of such arrangements
in Glansicystis baccata (Forbes). A
specimen of P. faberi in the University
of Iowa collection (SUI 39514) also has
combined A10—11 and A8—9 into single
plates. If P. faberi represents the more
primitive platycystitid form, then the
apparent increase in number of major
thecal elements in P. cristatus and
P. infundus may be both a phenotypic
and genotypic response to a changed life
habit (i.e. recumbent versus erect theca).
In the 3 known species of Platycystites
there is a direct correlation between the
number of thecal plates and the degree
of thecal inflation; the highly inflated
P. cristatus has the largest number
of regular and intercalate plates while
the compressed P. faberi has the least
of both. As might be expected P. infundus
has intermediate numbers of both plate
types.
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Many of the differences in plate pro-
portions between the 2 species may
similarly be interpreted as due to indi-
vidual variation rather than as valid
specific features. Some undoubtedly
result from unlike thecal outlines. Gross
shape varies somewhat from individual
to individual in P. cristatus but is a
useful taxobasis if used cautiously. The
holotype of P. infundus falls outside
the normal range of variation of P.
cristatus as regards thecal shape. Prob-
ably the greater area of the upper marginal
plates in P. infundus, which is related
to the degree of extension of the arm
tracks, is also not simply a feature of
this particular specimen. The flattening
of the right side of the holotype of P.
infundus is not due to distortion but
appears to be an original feature. We
believe that it served to stabilize a theca
which was recumbent on the sea bottom;
in fact the fossil specimen is stable at
rest in the position illustrated in figs. 9
and 10. The orientation of the stem facet,
which is diametrically opposite to that
of P. cristatus, (compare figs. 2 and 4)
is consistent with this interpretation.
Other points of difference between the
2 are likely of minor importance or
cannot be evaluated on the basis of
present material. P. infundus has a
coarser pustulate prosopon on the plate
surfaces than typical P. cristatus; but
similar specimens of the latter have been
observed. The small number of inter-
calates in P. infundus could be an artifact
of limited material; we believe, however,
that this feature is specific to the species.
With its flat right side and less expanded
theca (P. cristatus is greatly inflated in
this area) there is less need for extra
thecal elements.
Altogether we feel that there are
enough points of difference of signif-
icance to justify the separation of the
‘‘Oklahomacystis zone’? specimen from
Pcristatusat the specific Jevel.<in
spite of the lack of a large group of
similar specimens. In terms of gross
thecal morphology and plate arrange-
ment, P. infundus is closer to P. cristatus
217
than to P. faberi and has most likely
evolved from the former species.
Functional Morphology
Two current interpretations of the
life habit of Paracrinoidea (and Platycys-
tites) have the theca strongly canted to
the right, with the peristome uppermost
and the tips of the epithecal arms de-
fining a plane parallel to the substrate
surface. Parsley and Mintz (ibid, p. 22)
believed that the theca was raised off
the sea bottom by the stem, which would
have been relatively rigid. Conversely,
Durham would place the near horizontal
arm termination plane at the sediment-
water interface. In this model the theca
would be partly buried with the possibly
distally flexible stem serving as a sub-
surface anchor (ibid, p. 22, test-fig. 6).
A third possibility is that the paracrinoid
stems were ‘“‘runners’’ somewhat in the
manner of calceocrinids with the theca
lying on the substrate surface, peristome
uppermost, tethered by its stem. Parsley
and Mintz’s interpretation is most plausi-
ble for the majority of paracrinoids which
are not strongly asymmetric. For genera
like Platycystites we believe that Dur-
ham’s hypothesis is more plausible. The
addition of P. infundus to the genus
provides some additional information
on Platycystites mode of life.
In their discussion of Platycystites
Parsley and Mintz (ibid., p. 69) con-
sidered P. faberi and P. cristatus col-
lectively, as though both were func-
tionally and morphologically identical:
actually they have quite different morpho-
logical features. The restoration of
P. cristatus which they illustrate (ibid. ,
text-fig. 6), reflecting the opinion of J.
Wyatt Durham on its living position, is
probably most nearly correct for this
species and for P. infundus, but it very
likely does not apply to P. faberi. The
situation in Platycystites might be more
complex than visualized by previous
authors.
P. faberi has a thin compressed pear-
Shaped theca with the peristome and
columnar attachment area forming a
218
vertical axis. Both the right and left
epithecal arms extend from the mouth to,
or nearly to, the column. The animal
was almost perfectly bilaterally sym-
metrical and was no doubt held above
the substrate on a column. No complete
specimens are known; hence it is not
possible to determine with certainty
whether or not the theca was canted by
a flexure of the proximal column as
Parsley and Mintz (ibid., text-fig. 1)
illustrate for Amygdalocystites florealis
and infer for most paracrinoids. We
believe that the horizontal plane defined
by the arm terminations reflects the
living orientation in all paracrinoids;
we suspect that the theca of P. faberi
was not canted and that the supporting
column continued from its junction with
the theca, unbent proximally and aligned
with the longitudinal axis of the theca.
Like the theca, the column of P. faberi
was probably usually upright and verti-
cal. In this position the periproct would
be offset slightly to the right of the
peristome while the peristome, gono-
pore, and hydropore would be upper-
most. The periproct would thus be at a
slightly lower level than the peristome
and associated thecal openings, thus
tending to remove anal wastes from its
vicinity. It is difficult to conceive of
any manner in which fouling of the
subvective appendages could be avoided
if the theca of P. faberi were in contact
with or partly buried in the substrate.
P. cristatus and P. infundus have modi-
fied the theca to a strongly asymmetric
shape. P. cristatus is greatly inflated on
the right side proximal to the column;
this area of the theca is broadly rounded.
The equivalent thecal surface in P.
infundus is flattened and the theca is not
as rounded in profile. As noted by
Durham (in Parsley and Mintz) the right
arm of P. cristatus is always short
and does not extend into the expanded
area proximal to the column which is
presumed to contact the sea floor; the
right arm track of P. infundus is similarly
limited. Conversely, in both species the
left arm, which would be above the sea
floor in Durham’s and our reconstruc-
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
tion, extends nearly the full length of the
left side of the theca; in some specimens
it may even extend onto the column.
These features are shared with Amyg-
dalocystites florealis, which also may
have had the theca in contact with the
substrate. Possibly the same 2 modes of
living postulated for Platycystites had
their equivalents in Amygdalocystites:
most species, like A. florealis, have a
bend in the column proximal to the theca,
but the poorly known A. radiatus appears
to lack it (Parsley and Mintz, p. 51).
An undescribed species of Amygdalo-
cystites from the Dunleith (Middle
Ordovician) of northern Iowa, currently
being studied by T. W. Broadhead
(University of Iowa), has a proximally
unflexed column and 2 long equal
epithecal arms. Its thecal shape is similar
to that of P. faberi and its life habitus
was probably comparable. If the erect
life orientation suggested by Parsley
and Mintz were correct and universal
within these 2 genera we see no reason
why both arms in all species should not
be equal in length. It is probable, in our
opinion, that major differences in thecal
symmetry within a genus reflect differing
life habits, especially if modifications of
symmetry correlate with other morpho-
logical changes. A thecal morphology
and arm arrangement comparable to that
of P. faberi is present in other echino-
derm classes; at least | similarly-shaped
rhombiferan (Pseudocrinites) has 2 re-
cumbent ambulacra extending down the
theca onto the column. The Parsley and
Mintz model would, we feel, require
the column to be strong and relatively
rigid throughout its length; however
complete columns are exceedingly rare.
Not uncommonly specimens of A.
florealis and P. cristatus do retain the
proximal flexed, presumably ankylosed,
part of the column. This is more con-
sonant, in our opinion, with Durham’s
model or with a bottom-runner life habit.
Pronounced asymmetry of the theca
accompanied by a small column which
may be bent abruptly backward next to
the theca is not uncommon in other
paracrinoids. According to Hudson
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
(1905) the stem of Canadocystis emmonsi
‘“‘appears to have been short and used
perhaps for an anchor, but not for com-
plete support.’’ Hudson further suggests
that the ancestors of these paracrinoids
*“were once supported by the stem alone
and had their arms in a normal position,
but that descendants with weak stems
often found themselves let down to the
ocean floor and had to make shift to
live under adverse conditions. Increased
growth of the posterior side or de-
creased growth of the anterior plates
would have brought the arms again
uppermost to a form like that shown
here.’ Allowing for differences in termi-
nology and emphasis the theme of
Hudson’s observations is not far removed
from our conclusions herein.
Durham (in Parsley and Mintz) be-
lieved that there was a discernable
difference in prosopon below the sup-
posed termination plane in some speci-
mens of P. cristatus. We, like Parsley
and Mintz, have been unable to detect
this difference on the specimens we
have examined; but this does not in our
opinion weaken Durham’s argument in
any way. Other counterarguments ad-
vanced by Parsley and Mintz (p. 22)
also do not seem compelling. Preserved
columns of Amygdalocystites and Platy-
cystites with the cited morphological
features (proximal flexure and ankylosis)
are quite short, and it is not surprising
that they do not show a distal taper.
Comarocystites undoubtedly has a hold-
fast and relatively long straight column
and almost certainly was held erect; but
this genus does not show pronounced
thecal asymmetry or a differential expan-
sion of one side of the theca. Holdfasts
and lengthy stems have not been reported
for Platycystites or Amygdalocystites.
We do not believe that either Durham’s
model or that of Parsley and Mintz
apply to all paracrinoids. If the Para-
crinoidea is a valid taxon of class rank
it would be surprising if one mode of
living was adopted by all members;
considering the morphologic diversity of
the known paracrinoids this possibility
becomes vanishingly small. Investigation
219
of each paracrinoid genus individually
might yield more accurate information
about the class’ paleoecology than does
the attempt to apply a single over-
extended, albeit useful, model to the
class in toto.
Information about the length of the
entire column and the nature of the
adult attachment device, if any, in
Platycystites is lacking. It is worth
noting, however, that a possible future
find of a long column and holdfast in a
species like P. cristatus would not
necessarily invalidate Durham’s hypoth-
esis. The reconstruction in Parsley and
Mintz shows an abrupt stem termination,
but it is possible that the species was
attached when young and lost the stem
terminus as it approached maturity.
Alternatively it is also possible that the
theca merely lay on the surface of, rather
than partly embedded in, the substrate.
If such were the case the largely flexible
stem, doubled back under the theca,
would have served as a tether of a theca
which could adjust its living position in
a manner analogous to that suggested by
Kesling and Sigler (1969) for the Calceo-
crinidae: in this model the length of the
stem is irrelevant, and in fact calceocrinid
stems shorter than the crown or many
times its length have both been reported
(Brower, 1966). Like Parsley and Mintz
we postulate that many paracrinoids were
rheophilic; our model, or a modification
of Durham’s, would give the animal a
greater ability to adjust to a changing
current regimen than would that of
Parsley and Mintz. In either case the
streamlined bilaterally symmetrical theca
and concomitantly reduced subvective
system are supportive of a rheophilic
habit. Definitive evidence allowing the
elimination of one or the other major
alternative interpretations of living posi-
tion has not yet appeared.
Acknowledgments
This manuscript has benefited from
criticisms and suggestions by Thomas W.
Broadhead (University of Iowa). We
220
thank James Sprinkle (University of
Texas at Austin) for reviewing an earlier
draft.
References Cited
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echinoderms from Oklahoma. American Jour.
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Bather, F. A. 1900. The Echinoderma. Treatise
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Breimer, A., and D. B. Macurda, Jr. 1972. The
phylogeny of the fissiculate blastoids. Koninkl.
Nederl. Akademie van Wetenschappen Amster-
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Breimer, A., and G. Ubaghs. 1974a. A critical
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. 1974b. A critical comment on the classi-
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Brower, J. C. 1966. Functional morphology of
Calceocrinidae with description of some new
species. Jour. Pal., 40(3): 613-634.
Fay, R. O., and A. A. Graffham. 1969. Bromide
Formation on Tulip Creek and in the Arbuckle
Mountains Region. Regional Geology of the
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Hudson, G. H. 1905. Contributions to the fauna
of the Chazy Limestone on Valcour Island,
Lake Champlain. New York St. Museum, Bull.
80: 270—295, illus.
Kesling, R. V. 1968. Paracrinoids, in Moore, R. C.
(ed.) Treatise on Invertebrate Paleontology,
Part S. Geol. Soc. Amer. & Univ. Kansas
Press: pp. 268-288, illus.
Kesling, R. V., and J. P. Sigler. 1969. Cunctocrinus ,
a new Middle Devonian calceocrinoid from
the Silica Shale of Ohio. Univ. Michigan Mus.
Pal., Contr., 22(24): 339-360, illus.
Kirk, E. 1911. The structure and relationships of
certain eleutherozoic Pelmatozoa. U. S. Nat.
Mus. Proc. 41, 137 p., illus.
Macurda, D. B., Jr. 1973. The stereomic micro-
structure of the blastoid endoskeleton. Univ.
Michigan Mus. Pal., Contr., 24(8): 69-83, illus.
Matsumoto, H. 1929. Outline of a classification of
Echinodermata. Sci. Repts. Tohoku Univ.
Sendai, 2nd ser. (Geol.) 13(2): 27-33.
Miller, S. A. 1889. North American palaeontology
for the use of amateurs, students, and scientists.
Cincinnati, Ohio, 664 p.
Parsley, R. L. 1975. Systematics and functional
morphology of Columbocystis, a Middle Ordovi-
cian ‘‘Cystidean’’ (Echinodermata) of uncertain
affinities. Bull. Amer. Pal., 67(287): 394-361,
illus.
Parsley, R. L., and L. W. Mintz. 1975. North
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American Paracrinoidea: (Ordovician: Para-
crinozoa, new, Echinodermata). Bull. Amer. Pal.
68(288), 113 p., illus.
Paul, C. R. C. 1967. The British Silurian Cystoids.
British Mus. (Nat. Hist.), ser. A (geol.) 13:
297-356, illus.
-- 1968. Notes on cystoids. 2. An unusual
arrangement of thecal plates in Glansicystis
baccata (Forbes).Geol. Magazine, 105(4): 416-
417.
Regnell, G. 1945. Non-crinoid Pelmatozoa from
the Paleozoic of Sweden. Lunds Geol.-Min.
Inst., Medd. 108, 25S p., illus.
Sinclair, G. W. 1945. Some Ordovician echinoderms
from Oklahoma. Amer. Midland Nat., 34(3):
7077 low illus:
Springer, F. 1913. Cystoidea. In Zittel-Eastman,
Text-book of Paleontology, 1: 145-160, Mac-
millan, London.
Sprinkle, J. 1973. Morphology and Evolution of
Blastozoan Echinoderms. Harvard Univ., Mus.
Comp, Zools ‘Spee. Pub:, 283 p:
Evolutionary and Paleoecologic Significance
of Abnormal Platycystites cristatus Bassler
(Echinodermata: Paracrinoidea)
T. J. Frest and H. L. Strimple
Department of Geology, University of Iowa, Iowa City, Iowa 52242
ABSTRACT
Two specimens of the common Bromide Formation (Middle Ordovician; Oklahoma)
paracrinoid Platycystites cristatus Bassler have 3 epithecal arms instead of the normal
2. Analysis of the location and mode of branching of these specimens supports the
suggestion of Parsley & Mintz (1975) that the paracrinoid ancestor had 2 epithecal arms.
One specimen also has a portion of a column embedded in its right side; the column
location and thecal shape indicate that the life position of the animal was with the theca
recumbent on the sea floor.
Three-Armed Platycystites cristatus
The rare fossil echinoderm class Para-
crinoidea (Regnéll, 1945) exhibits con-
siderable morphologic diversity despite
its restricted range and distribution
(Middle-Upper Ordovician, almost ex-
clusively North American) and the small
number of member taxa (9 genera) as
presently known. Only 2 species, Platy-
cySstites cristatus Bassler and Oklahoma-
cystis tribrachiatus (Bassler), are repre-
sented by large numbers of individuals.
The class recently has been monographed
comprehensively by Parsley & Mintz
(1975). While their work was primarily a
taxonomic treatment of North American
paracrinoids they also briefly present
some data bearing on the phylogeny of
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
the group (Parsley and Mintz, 1975:
11-15). Their tentative comments are
based on the assumption that the so-
called cystidean transverse arm pair is
more primitive than the triradiate con-
dition favored by some authors (Parsley
and Mintz, 1975: 12, footnote). More
particularly they infer that the primitive
subvective condition in paracrinoids was
also a primary transverse pair of epithecal
arms, and that the exothecal, more-than-
2-armed condition present in some genera
of both paracrinoid orders is more ad-
vanced. Those genera which have more
than 2 arms (e.g. Oklahomacystis) are
believed to have acquired the extra
subvective elements by branching of | or
both members of the primary pair
(Parsley and Mintz, 1975: 11).
221
The acquisition of an extra arm
probably is a solution to the problem
of increasing the proportion of subvective
area relative to the total thecal volume:
this would increase food gathering
capacity and hence make the species a
more effective competitor with other
echinoderms. Secondarily, an absolute
increase in surface area devoted to food
gathering could presumably support a
larger theca. Development of additional
arms could come about in two ways:
bifurcation of the primary pair distal to
the peristome or addition of wholly new
arms at the peristome. In the latter case
extra arms extending anteriorly are more
probable since the external and internal
water-vascular system, gonopore, and
anus frequently are all posterior in
position. The pentaradiate condition
would originate from utilization of both
alternatives; this would explain the
bipentaradiate (2-1-2) appearance of
the ambulacra of many echinoderms
(Sprinkle, 1973: 42-43).
The Paracrinoidea exhibit a range of
arm conditions demonstrating independ-
ent use of both mechanisms of arm
increase. Two-armed genera (Sinclairo-
cystis, Amygdalocystites, Platycystites ,
Canadocystis, and Malocystites) may
have the arms either transversely or
sigmoidally arranged; invariably they are
dominantly or completely epithecal.
The minority of genera with 3 or more
arms (Comarocystites , Oklahomacystis ,
Achradocystites, and Wellerocystis) are
evenly split between epithecal and exo-
thecal forms. Three of the 4 definitely
dichotomize 1 or both primary arms;
Achradocystites apparently bifurcates
the left arm, but so near to the peristome
that the branch can be regarded as an
independent third arm (Parsley & Mintz,
op. cit., p. 15). Oklahomacystis also
normally has 3 arms; the third results
from a division of the left primary near
the peristome.
Primacy in the Paracrinoidea of the
transverse pair over a triradiate con-
dition has not been conclusively estab-
lished, largely due to the limited strati-
graphic range and size of the class. How-
222
ever, the earliest paracrinoids, Chazyan
in age, do possess only 2 arms. Neither
Chazyan genus is likely to resemble
closely the paracrinoid ancestor; Malocy-
stites is ‘“‘morphologically the most
specialized genus the Paracrinoidea’’
(Parsley and Mintz, op. cit., p. 90) and
the thecal plates of Canadocystis , which
lack a sutural pore system, are probably
secondarily specialized (Parsley and
Mintz, op. cit., p. 57). In the absence
of a lengthy geologic record other lines
of evidence can be developed to recon-
struct the class phylogeny. Study of
morphological variants in large popula-
tions may be of use in this connection.
If the overall trend in the Paracrinoidea
was toward increased subvective effi-
ciency, occasional 3-armed variant indi-
viduals in characteristically 2-armed
species might be expected. The position
of the third arm could provide data
indicating either the biradiate or tri-
radiate condition as ancestral. In the
former case one would expect the addi-
tional arm to be anterior for the reasons
cited above, but constancy of either
position or point of origin is unlikely.
If the triradiate condition were primitive,
the third arm is not additional but re-
capitulates the ancestral condition. In
this case the third arm should also be
anterior in position but most likely would
originate at the peristome rather than as
a branch of one or the other transverse
arms, and laterally it should be equidis-
tant from both transverse members.
One 3-armed specimen of the usually
2-armed Sinclairocystis praedicta Bassler
was mentioned by Parsley and Mintz
(op. cit., p. 43, pl. 3, figse9>i0) aie
left arm of this specimen bifurcates near
the peristome and the anterior branch of
this arm is also divided near its end.
Three-armed Platycystites cristatus Bass-
ler have not been reported previously:
the 2 specimens described below are in
the collections of the Department of
Geology, University of Iowa (SUI).
SUI 39518 is a large (diameter 32 mm)
well-preserved specimen typical in all
respects except in the possession of an
extra arm (figs. 3-6). The third arm
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Figs. 1-6.—Photographs of abnormal Platycystites cristatus. 1-2, basal and top views of SUI 39517
showing embedded stem and third arm, X2.7. 3-6, anterior, top, basal, and posterior views of SUI 39518,
showing thecal morphology and arm configuration, X2.7.
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976 223
arises from a bifurcation of the right
primary near the peristome (fig. 4). Its
length is approximately equal to that
of the transverse right arm (17.8 mm).
Calluses for all 3 arms are well developed
and subequal in average width (fig. 3).
The lumen is prominent in the vicinity
of the peristome along the primary pair
but does not extend into the third arm
(fig. 4). From its origin immediately to
the right of the peristome the third arm
traverses AS and A2 before curving onto
A7, where it terminates. The point of
termination is abrupt and lies just above
the termination plane defined by the pri-
mary pair (fig. 7). A smaller specimen
(SUI 39517: diameter 16 mm) also has
a thecal plating arrangement within the
normal range of variation for the species.
Thecal shape in this specimen is some-
what distorted from the norm by the
presence of part of an echinoderm column
embedded in its right side (figs. 1, 8).
A third arm results from a bifurcation
of the left member of the primary pair
on the anterior face. As in SUI 39518
the extra arm does not extend below the
termination plane defined by the primary
arms and is short, but well developed.
The point where arm division occurs in
this specimen is also near the peristome.
An extension of the lumen into the
third arm is present but is narrower and
shorter than those in the other two arms
(fig. 2). Beginning on A4 the anomalous
arm intersects A3 and extends across
L3 nearly to the A1l-L3 junction before
terminating (fig. 7).
Despite the small number of three-
armed P. cristatus some reasonable
inferences about the phylogenetic signif-
icance of the extra arm can be made.
Both hypotheses (i.e biradiate vs. tri-
radiate class radical) suggest that the
third arm should be developed on the
anterior face; this is the case for both
P. cristatus and S. praedicta. Most of
the evidence, however, is more in accord
with Parsley and Mintz’ hypothesized
biradiate ancestor than with a triradiate
one. The position of the extra arm is not
fixed, it arises from a division of either
224
member of the primary pair rather than
from the peristome border, and it is not
equidistant from the other arms. A well-
developed lumen is not present; this is
more consonant with the position that
the third arm is additional, rather than
a retained archaic feature. We concur
with the suggestion of Parsley and Mintz
that the need for a greater amount of
subvective surface area leads to the
acquisition of more than 2 arms in many
paracrinoids. The paleoecology of P.
cristatus 1s also supportive of this inter-
pretation. Like Durham (in Parsley and
Mintz, op. cit.) we believe that at least
some species of Platycystites had the
theca in contact with the substrate (Frest
et al., 1976). P. faberi Miller, which
most likely was elevated above the sea
bottom by its column, has both transverse
arms nearly or exactly equal in length
and extending nearly to, or even onto,
the column. If the subvective system’s
area is closely related to arm length,
P. faberi would have been more effi-
cient in food gathering than P. cristatus
due to its longer arms relative to thecal
volume. The right arm of both P. crista-
tus and P. infundus is much shorter
than the left. These 2 species are also
more inflated in cross section than the
laterally compressed P. faberi. We have
suggested elsewhere (Frest et al., op.
cit.) that thecal asymmetry and broader
thecas in some paracrinoids are adapta-
tions to arecumbent habit (with peristome
uppermost) and that shortening of the
right arm in such forms is a mechanism
to avoid fouling of the arm by sediment.
The 2 genera in which 3-armed specimens
have been reported both display this
plexus of features. The advantages of a
recumbent habit, especially less com-
petition from other echinoderms, may
have outweighed the disadvantages of a
reduction subvective area; but it is
probable, in our opinion, that the addi-
tion of a third arm was in part com-
pensatory for the length loss suffered by
the right arm in adaptation to a spe-
cialized environment. The recumbent
habitus of some species may have en-
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Figs. 7-9.—Plate diagrams of Platycystites cristatus. 7, composite showing positions of thecal
plates and paths of epithecal arms (black). 8, right view of SUI 39517, showing thecal plate configuration
and embedded column. 9, right view of typical specimen of P. cristatus, showing usual thecal plate
pattern.
couraged arm incrementation over and
above the general trend in the Para-
crinoidea and other classes.
If the case presented herein for a
primitive biradiate condition in the
Paracrinoidea is far from conclusive, it
is nonetheless suggestive. Demonstra-
tion of the phylogenetic antiquity of the
‘“‘cystidean’’ transverse arm pair in at
least 1 primitive echinoderm class (or
subphylum, according to Parsley and
Mintz) is strongly supportive of Ubaghs’
postulated bilaterally symmetrical motile
Precambrian ancestor for the Echino-
dermata (Ubaghs, 1968: S47) and further
Suggests that the primitive bilateral
condition may have been maintained un-
altered in some echinoderm classes,
which would not have passed through a
triradiate stage, as hypothesized by
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Caster (in Ubaghs and Caster, 1968;
1971). Both views assume an originally
bilateral motile primordial form gave rise
to all subsequent classes monophyletically
some time before the beginning of the
Paleozoic, but they diverge strongly on
the origins and universality of the
radially symmetrical strategy adopted
by most later echinoderms.
Thus far most attention in attempts to
resolve this problem has been focused
on the ‘‘carpoid’’ classes (Subphylum
Homalozoa), whose apparent bilateral
symmetry, or asymmetry, has long been
recognized. Ubaghs (op. cit., 1969)
believes that the primordial bilateral
symmetry persists in the Homalozoa
while Caster has argued that the carpoids
are ‘‘bilateralized derivatives of a hypo-
thetical tri-radiate (presumably sessile)
225
ancestor’ (Caster, 1971: 919). Most
echinoderm classes have yet to be as
thoroughly examined. Some classes un-
doubtedly do exhibit primitive triradiate
symmetry (e.g. Edrioasteroidea: Bell,
1976).
Sprinkle (op. cit., p. 42—43) has specu-
lated that the change to a triradiate con-
dition in the echinoderms was brought
about by the development of a means of
attachment and a plated subvective sys-
tem early in the phylum’s history. These
2 developments would also, according to
Sprinkle, engender a modification of the
subvective system toward radial sym-
metry, primarily as a response to the
acquisition of a filter-feeding habit.
Since the most fundamental adaptation
was related to feeding, the subvective
system would probably be the first to
adopt the new pattern of symmetry.
While this reasoning is plausible for
most echinoderm groups it may not be
applicable to all. Some paracrinoids (e.g.
Comarocystites) were certainly attached
to the bottom by a column and a stem
facet, as contrasted with a holdfast
(sensu Sprinkle, 1969: see also Sprinkle,
1973: 36-40), is present in all known
species; but both Parsley and Mintz and
we have presented evidence for the per-
sistence in the Paracrinoidea of a bi-
laterally symmetrical transversely ar-
ranged subvective system in animals
which had thoroughly adopted them-
selves to an attached, filter-feeding habit.
If, as we suspect, the sessile Para-
crinoidea are fundamentally bilaterally
symmetrical and have not passed through —
a radially symmetrical stage, it becomes
more plausible that the triradiate stage
is lacking in the ancestry of the Homalo-
zoa as well. The existence of both
sessile and motile non-radiate echino-
derm classes indicates that the primordial
condition may be more persistent than
formerly believed, and perhaps is more
widespread than currently accepted.
Studies of symmetry patterns and devia-
tions from them are lacking for most
echinoderm classes, so that the func-
tional and phylogenetic significance of
226
both patterns cannot yet be adequately
evaluated.
Paleoecology of Platycystites cristatus
Available evidence concerning the
life-habits of Platycystites has recently
been reviewed by Frest et al., (op. cit.),
who argue for a recumbent habit for
P. cristatus and P. infundus but an erect
habit for P. faberi. A single abnormal
specimen of P. cristatus with an em-
bedded echinoderm column provides
additional evidence for a recumbent habit
in this species. This specimen (SUI
39517) is also triradiate, as described
above. The column fragment is embedded
along the right side of the theca (figs. 1, 8)
extending from RB onto the intercalate
proximal to RB. The shape of the theca
has been distorted somewhat in this area,
presumably a response of the living ani-
mal to the column, but the plate con-
figuration of the specimen is within the
normal limits of variation in P. cristatus;
a plate diagram of the equivalent area
on a normal specimen (SUI 39516)
is included for comparison (fig. 9).
Several features of the specimen indicate
that the stem became lodged in the
theca during life. The column does not
lie on the plates’ surface, but is incised
partly into the theca. During growth it
has been laterally encroached upon and
partly overgrown by the surrounding
plates; the diameter at the best exposed
end is greater than the exposed width of
the column measured normal to its long
axis. The involved plates are well-
preserved, floor the groove underneath
the stem as well as making up its walls,
are clearly not fractured or broken, and
appear to have been thickened proximal
to the stem by secretion of secondary
stereom. Plates of Platycystites are
typically very thin and, one would sup-
pose, not very resistant to deformation
after death or during the fossilization
process. The column itself is not as well
preserved, and its identity cannot be
established with certainty from its mor-
phology as now known. Its position,
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
nearly astride a line passing from the
stem facet to the base of the right arm
and upward to the peristome, may be
taken to indicate that the column is that
of the animal in which it is now em-
bedded, but several lines of evidence
militate against this conclusion. The stem
portion is not precisely aligned as would
be expected; an irregular flexure of the
stem proximal to the facet would be re-
quired to connect the retained portion to
the stem facet. The end most distant from
the stem facet terminates in the theca and
is poorly exposed. Proceeding from the
stem facet, the embedded fragment be-
comes more deeply ‘‘buried.’’ Platy-
cystites cristatus columnals are generally
much narrower than those of the em-
bedded specimen (fig. 1). All 3 current
interpretations of Platycystites’ living
position presuppose that at least the
proximal part of the stem is functional
throughout life; hence it should be as
well-preserved as the adjacent, much
thinner, thecal plates. We believe that the
stem is a foreign object and not that of
Platycystites; the alternative cannot,
however, be categorically rejected on
present evidence.
Review of the previously suggested
paleoecologic interpretations in relation
to this specimen allows a choice to be
made among them regardless of the
specific identity of the stem. Were the
theca held erect (Parsley and Mintz
model) a foreign object is unlikely to
have become lodged in the theca’s right
side, which would be the exposed “‘bot-
tom’’ (Parsley and Mintz, text-fig. 1),
i.e. lowermost, but still considerably
above the sediment-water interface. If
the stem belongs to the specimen, the
theca could not have been erect through-
out its life span; one end appears to
terminate in the theca. Even if the
column did not terminate in such a man-
ner, embedment would considerably im-
pair the ability of the theca to adjust its
position in this model and the animal
would effectively have been fixed in a
single position. Fixation of this part of
the animal’s stem would not greatly
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
impede its operation if it functioned as
an anchor (Durham model) or as a tether
(our model). If the stem belongs to the
theca and does normally terminate near
the point exhibited by this specimen,
function as an anchor is most probable
among the three models. However
Parsley and Mintz (op. cit., pl. 8, figs.
1-3) do illustrate 1 specimen with a
longer column. Alternatively it is possi-
ble that the stem became non-functional
as the animal matured and the unattached
negatively bouyant adult theca lay on or
partly buried in the substrate, with the
peristome uppermost. Assuming that the
stem is a foreign object, the tether model
becomes most likely true. A theca buried
in a soft substrate is less likely to en-
counter or be damaged by a hard object
than is a theca in contact with the
substrate surface and perhaps capable
of being moved over it by currents; but
the point is not particularly telling.
Overall inferences based on this speci-
men are supportive of either the anchor
or tether hypotheses, but weigh heavily
against the assumption of an erect habit
in P. cristatus.
James Sprinkle (pers. comm., 1976)
has suggested that the deposition of
secondary stereom could indicate
secondary repair of damage to an
originally erect theca that has been
‘tipped over and injured . . . hanging
on for dear life.’’ While it is difficult
to imagine how an accident with the
observed results could happen to an erect
theca, the possibility cannot be disre-
garded totally. Minimally, however, it
suggests to us that a paracrinoid could
survive recumbent on the sea bottom
for a lengthy period of time—sufficient
to allow extensive secondary secretion
of stereom. Since the thecal shape has
been influenced and there is no sign of
plate fracturing around the embedded
column we suspect that the column may
have been encountered early in the ani-
mal’s growth and did not greatly impede
later growth or cause the animal’s
demise.
227
References Cited
Bell, B. N. 1976. A study of North American
Edrioasteroidea, N. Y. State Mus. Sci. Service,
Mem. 21, 447 p.
Caster, K. E. 1971. Review of Les Echinodermes
Carpoides de l’Ordovicien Inferieur de la Mon-
tagne Noire (France), by G. Ubaghs, Jour.
Pal., 45: 919-920.
Frest, T. J., H. L. Strimple, and M. R. McGinnis.
1976. A new species of Platycystites (Echino-
dermata: Paracrinoidea) from the Middle Ordo-
vician of Oklahoma. Washington Acad. Sci.
Jour., 66: 211—220.
Parsley, R. L., and L. W. Mintz. 1975. North
American Paracrinoidea: (Ordovician: Para-
crinozoa, new, Echinodermata). Bull. Amer.
Pal., 68 (288), 115 p.
Regnell, G. 1945. Non-crinoid Pelmatozoa from
the Paleozoic of Sweden. Lunds Geol.-Min.
Inst., Medd., 108, 255 p.
Sprinkle, J. 1969. The early evolution of crinozoan
and blastozoan echinoderms (abst.). Geol. Soc.
Amer., Spec. Pap., 121: 287-288.
1973. Morphology and Evolution of
Blastozoan Echinoderms. Harvard Univ., Mus.
Comp. Zool., Spec. Pub., 283 p.
Ubaghs, G. 1968. General characters of Echino-
dermata. In Moore, R. C. (ed), Treatise on
Invertebrate Paleontology, Part 5, Echino-
dermata I (1), Geol. Soc. Amer. and Univ. of
Kansas Press: p. S4—SS9.
. 1969. Les Echinodermes Carpoides de
VOrdovicien Inferieur de la Montagne Noire
(France). Cahiers de Paleontologie, 112 p.
jand K. E. Caster. 1968. Homalozoa. In
Moore, R. C. (ed.), Treatise on Invertebrate
Paleontology, Part S, Echinodermata 1 (2),
Geol. Soc. Amer. and Univ. of Kansas Press:
p. S495—S634.
Web-spinning eriophyid mites!
L. C. Knorr, H. C. Phatak, and H. H. Keifer
Project Manager, UNDP/FAO Plant Protection Service, clo UNDP, GPO Box 618,
Bangkok 5, Thailand; Virologist, Danish International Development Agency,
clo Department of Agriculture, Ministry of Agriculture and Cooperatives, P. O.
Box 10, Bangkhen, Bangkok 9, Thailand; and Collaborator, USDA Agricultural
Research Service, c/o California Department of Agriculture, Sacramento, CA 95814,
U.S.A., respectively.
ABSTRACT
The literature contains no mention of spinning among the Eriophyoidea; neither do
anatomical studies suggest the presence of spinneretlike organs in this group of
microscopic 4-legged mites.
Large colonies of an eriophyid mite, newly described as Aculops knorri Keifer,
were encountered under weblike coatings on leaves of Lepisanthes (= Erioglossum)
rubiginosa (Roxb.) Leenth. Attempts were made to determine whether the coatings
are a host response to mite feeding or whether they consist of silklike strands
emanating from the mite itself. Serological indications are that the strands, 0.3-0.6 uw
wide, are proteinaceous in nature and are antigenically closely related to the mite.
As far as known, these findings constitute the first report of spinning among the
Eriophyoidea.
Although web spinning is common
among many spiders and spider mites,
it has not been recorded to occur among
1 Contribution No. 1 of UNDP/FAO Plant Pro-
tection Project THA 74/019.
228
eriophyid mites. Neither have spinneret-
like structures been detected in anatomi-
cal studies of these microscopic worm-
like mites (Keifer, 1976).
Recently a report from the Sudan
(Hassan and Keifer, in press) described
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
a coating on mango leaves infested with
the eriophyid Cisaberoptus kenyae Kei-
fer. Incidentally, the same coating and
mites are also found on mango in Thai-
land and the Indonesian island of Bali
(Knorr, unpublished information). The
- coating is characterized as weblike, but
the Sudanese report does not undertake
to show that the covering is spun by the
eriophyid.
The following account offers evidence
that such webbing is not only associated
with, but is the silklike product of, an
eriophyid mite. This would thus con-
stitute the first report of spinning among
the Eriophyoidea.
On 16 April 1975, the first author en-
countered a sapindaceous fruit tree,
Lepisanthes (= Erioglossum) rubiginosa
(Roxb.) Leenth., at Bangkhen, Thailand
with leaves exhibiting weblike patches
(Plate II, figs. 1, 2, 3). Similar patches
were later found in foliage of the same
host at Hua Hin, 170 km to the south.
A mango tree adjacent to the Bangkhen
tree showed no webbing, although
branches were intertwined with those
of the web-bearing Lepisanthes.
Under the patches, but seldom outside
of them, were large numbers of active
eriophyids (Plate III, fig. 1), subse-
quently identified by Keifer (1976) as a
new species, Aculops knorri. The only
unusual feature found to distinguish the
mite from others in this ‘‘wastebasket’’
genus was a thickening of the legs with
most of the increased size on the femora
(Plate I). No structures were seen that
might suggest web-spinning organs.
Web Morphology
The weblike patches occur almost
invariably on the adaxial surfaces of
Lepisanthes leaflets. Patches are at first
dull grayish white, resembling powdery
mildew. In later stages, the webbing
_ becomes shiny. The earliest visible trace
of webbing approximates the size of a
small pinhead; the largest expanse covers
nearly the entire leaflet (Plate II, fig. 2).
Elongate patches commonly border the
Main and lateral veins (Plate II, fig. 1).
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
~ a EEE i
WGP I
BEE aise
Tp
c a>
PLATE I: Aculops knorri Keifer, a web-
spinning eriophyid mite. Length of female from
anterior end of frontal shield lobe to end of
terminal lobes, 128-148 wp.
Incipient, pinhead-sized._ webs are often
disposed without relation to veins.
Webbing occurs throughout the canopy
of this 25-ft tree with approximately 5%
of the leaves affected.
Under 40x magnification and reflected
light, the patches seem to be amorphous
films although a suggestion of linearity
appears at higher magnifications. With
1000 magnification provided by a
scanning electron microscope, the films
are clearly disclosed to be made up of
fine criss-crossing filaments measuring
0.3 to 0.6 w in breadth (Plate III, figs. 4,
5). Adjacent to this tangle of loose
filaments, there is a consolidation of
threads to produce what appears to be a
woven or polymerized fabric (Plate III,
fear)
Between the patches and the leaf
surface, the stereomicroscope at 40x
reveals the presence of pale reddish-
brown adults, water-white nymphs, and
eggs of a homogenous population of
eriophyid mites that are disposed uni-
formly beneath the webbing (Plate III,
fig. 1). The occasional patch encountered
on the underside of leaves contains the
same mites, but even in old abaxial
patches mites remain water-white in
color. Mites are not particularly con-
centrated at, or aligned with, the periph-
eries of the patches. A young colony
0.5 mm in diameter generally contains
4 live mites. Larger concentrations of
mites under the upper-surface webs can
be made out with the naked eye as
reddish-brown dots. Peak infestations
and web formation occur from April to
the beginning of the monsoon rains in
229
PLATE II: Figs. 1-4: 1. Entire leaf of Lepisanthes rubiginosa with eriophyid webbing. 2. Leaflet
magnified. 3. Close-up of webbing. 4. Serological agar double-diffusion test for web antigens. Central
well (S) in agar charged with antiweb rabbit serum; peripheral wells charged with: A and B, mite
bodies in SDS-saline; C, D, and E, mite webbing in SDS-saline; F and H, host leaf scrapings in SDS-
saline; and G, purified host leaf proteins in SDS-saline. Note opaque, white precipitation bands
opposite all excepting the last 3 peripheral wells. The bands opposite B and C have fused (arrow)
without spur formation.
230 J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
PLATE III: Figs. 1-5: 1. Increased magnification showing eriophyids underneath webbing (black
arrow). Note reweaving of tear in original web (white arrow). 2. Webbing removed to show eriophyids
in contact with leaf surface. 3. A scotch-tape water mount of eriophyids from Fig. 2. 4 and 5. Scanning
electron micrographs of eriophyid and unconsolidated strands. In Fig. 5, note woven or polymerized
strands (arrow) that form the fabric of the webbing. (SEMs courtesy of the Danish Technological In-
stitute, Laboratory for Scanning-Electronmicroscopy, Copenhagen).
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976 231
June. New leaves that flush after the
start of the rainy season are apparently
free of webbing, even after 1 month.
Though no systematic counts were
made, there does not appear to be pre-
mature drop of affected leaves, nor do
leaflets heavily coated with patches show
any differences in growth when com-
pared with adjacent uncoated leaflets.
Under old patches, particularly alongside
midribs and lateral veins, there is a
slight russeting or necrosis of host
epidermal tissues.
Web Composition
In the absence of any information in
the literature that eriophyids spin, the
weblike patches were first thought to
represent a host response to feeding of
the mites. A second possibility con-
sidered was that the Aculops mites on
leaves of L. rubiginosa might inhabit
webs spun by other mites, but whereas
periodic observations over a year’s time
revealed the presence of Brevipalpus
phoenicis , Hemicheyletia sp. near bakeri,
Cunaxa sp., and Phytoseius spp., ‘‘none
of these mites could cause the spinning
associated with A. knorri’’ (E. W. Baker,
in correspondence). Furthermore, at no
time thoughout the year were webs found
that were unoccupied by the spinning
eriophyid. Two other eriophyids were
found (Acarhis lepisanthis Keifer and
Hyboderus roseus Keifer), but neither of
these new species occurred on the upper
sides of Lepisanthes leaves and neither
was associated with webbing (Keifer,
1975). Consideration was also given to the
possibility that the webbing might consist
of waxy filaments, since it is known that
certain eriophyids extrude wax.
A serological approach was taken to
determine whether the webbing was a
host artifact, a waxy secretion of the
eriophyid, or a mite-secreted silk similar
to the scleroproteinaceous filaments that
make up the webs of spiders.
Serological Methods and Materials
Production of web immunogen. — Host
leaves with apparently fresh webs and no
232
other contaminants were collected on
various occasions. They were washed
with slow-running tap water to remove
dust and debris, blotted gently with
filter paper, and stored in a moist
chamber until use the same day. Leaves
infested with spider mites were rejected.
Leaflets with typical webs were exam-
ined under alow power stereomicroscope,
and webs containing the fewest possible
eriophyids were carefully teased free of
adhering mites with a slightly blunted
stainless-steel needle cleaned in 90%
ethanol between use. In addition to ex-
cluding mites, care was also taken not to
scratch the leaf surface so as to prevent
contamination with host proteins. Several
hours of work were required to obtain suf-
ficiently concentrated web suspensions.
The mite-free webbing was placed in a
small volume of sterile distilled water.
Although desirable, a photometric deter-
mination of web concentration was not
made. The suspension was then poured
into dialysis tubing, gently squeezed to
break up the webbing, and dialized over-
night against normal saline (0.85% NaCl
in distilled water) in a refrigerator for the
removal of any toxic substances. Dialysis
was carried out for only the first injection
into rabbits.
Production of antiweb serum.—A 2-
year-old rabbit, weighing about 2.5 kg and
reared under laboratory conditions, was
used. Normal serum was collected a week
before the first injection. The animal re-
ceived 3.0 ml of the web suspension by
the intravenous route on 31 October, 1975.
It was followed by three injections of 2.0,
2.3, and 1.5 ml suspensions respectively,
on 4, 5 and 6 November. Four more intra-
venous injections of 1.2, 2.2, 2.0, and 2.0
ml were given to the same animal on 10,
12, 13, and 14 November, respectively.
Thus, 16.2 ml of web suspension were
injected in 8 instalments within 15 days.
The animal was bled 4 days after the last
injection and a 20 ml sample of blood was
collected. The blood was allowed to clot
for 2 hours at room temperature followed
by refrigeration overnight. The clot was
broken with a glass rod, the serum de-
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
canted and then centrifuged for 15 min
at 3000 rpm to remove corpuscular matter.
Sodium azide was added to the antiweb
serum as a preservative at final concen-
tration of 0.03% and the serum stored
at about — 15°C.
Serological tests.—A gel of 0.8%
Ionagar No. 2 (Colab, USA) containing
0.5% sodium dodecyl sulphate-SDS
(Sigma, USA) was made in normal saline
solution by autoclaving at 120°C, 15 psi
pressure, for 10 min. Sterile petri dishes
(100 mm diameter) were poured with 10 ml
hot agar containing 0.02% sodium azide,
which was allowed to solidify. Using a
flame-sterilised cork borer (No. 2, 4 mm),
test patterns were cut in agar in the form
of 6 or 8 peripheral wells around a slightly
larger (S mm) central well cut with No. 1
cork borer. Distance between closest
edges of the central and the peripheral
wells was 5—7 mm. Agar plugs were re-
moved with a pipette connected to a
vacuum line. Generally, 3 sets of 7 or 9
wells each were produced in 100-mm
petri dishes. Undiluted antiweb serum
was placed in the central well while
peripheral wells were charged with (1)
pure web suspension in saline, with or
withoutl, 2, or 3% SDS, (2) eriophyid
mite bodies in saline, with or without
SDS, (3) scrapings from the upper sur-
face of host leaves in saline, with or
without SDS. Controls were of normal
saline and SDS at the 3 concentrations,
and normal serum against all above treat-
ments. After charging the wells, the petri
dishes were maintained in a humid
chamber at room temperature up to
several days and observed daily in
transmitted, oblique lighting.
Results.—Positive reactions in the
form of characteristic white, opaque pre-
cipitation bands were observed within
48 hr between the antiserum-containing
central well and the peripheral wells
carrying web suspension with SDS, as
well as those charged with mite bodies
with SDS, but not the wells containing
host scrapings with or without SDS, even
after several days of incubation (Plate IJ,
fig. 4). Also, there were no reactions
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
with any controls. Precipitation bands
were absent when normal serum was
tested against any of the treatments—
web, mite, or host scrapings. The extent
of positive reactions of the antiweb
serum with webs and mite bodies was
comparable.
Discussion
Since utmost precaution had been
taken to avoid contamination of the web
preparations used for immunization, the
positive serological reaction of mite
bodies with antiweb serum indicates
relationship between the web and the
mite. Also, the immunogenicity of the
web is evident. The similarity of the
positive reaction of the web and the mite
bodies suggests that the latter share all
or nearly all antigen species with the
former. Absence of reaction with host
scrapings at the same time indicates
lack of any such relationship between
the web and the host leaf.
An alternate hypothesis was that the
webbing might consist of mite-secreted
wax. On the basis of serological evi-
dence, this now appears untenable since
waxes are not known to be immunogenic.
In order to confirm nonexistence of a
host relationship, it was considered
advisable to repeat the test with con-
centrated proteins from the host foliage.
The work was conducted following the
method of Shepard (1972). Young as well
as mature green leaves of L. rubiginosa
were collected free from mite infestation
and macerated in a Waring blender with
ice-cold 0.5 M borate buffer, pH 8.2,
containing 1% sodium sulfite and 0.01 M
magnesium acetate at the rate of 3 ml
buffer/g of foliage. The macerate was
filtered through a layer of cheesecloth
and shaken with cold chloroform (1:1 by
volume) for 30 min. The preparation was
centrifuged at 10,000 g for 10 min and
the aqueous phase recentrifuged at
80,000 g for 90 min. After discarding
the supernatant, the pellets were sus-
pended overnight in 1/30th the original
volume of 0.05 M Tris buffered-saline,
pH 7.2, containing 0.01 M magnesium
233
acetate. The protein preparation ob-
tained by this method was tested, with
and without dilution and SDS, against
the antiweb serum, but there was no
reaction.
It appeared that soluble protein species
are either lacking or are in too low con-
centrations to be detected by the gel dif-
fusion test, in web suspension as well as
in mite-body suspensions. Perhaps that
is why there was no reaction when SDS
was not used. There have been reports
on the use of SDS for degrading filamen-
tous plant virus particles for easier dif-
fusion in agar gel (Gooding and Bing,
1970; Purcifull et al., 1973, 1975). In the
present work, 3% SDS tended to produce
nonspecific turbidity in agar, and sub-
sequently only 1% SDS was used for
degrading presumably large molecules of
web proteins as well as mite-body pro-
teins into diffusable antigens.
The similarity in the extent of positive
reaction of web suspension and mite-
body suspension against antiweb serum is
not surprising if we accept that the mite
produced the webs. In that case the web
antiserum would be expected to have
antibodies against antigen species com-
mon to the web and the mite. On the
other hand, an antimite serum would
have given different qualitative as well
aS quantitative responses against the
mite and the web. Reciprocal testing
with antisera against mite-body proteins
and against normal host proteins would
have been desirable but has--not been
done. Nevertheless, there is a strong
indication that the eriophyid mite on
L. rubiginosa is involved in the produc-
tion of proteinaceous webs associated
with it.
Ultimate proof that the mite actually
234
spins must come from direct observation.
Efforts to demonstrate this have so far
not succeeded owing to the difficulty of
visualizing in situ the emanation of
strands only % uw wide. Neither have
attempts yet succeeded in transferring
mites to clean leaf surfaces in order to
observe web construction. There is, how-
ever, evidence of reconstruction in Plate
III, fig. 1, where tears in the original web
have been rewoven. Repair takes place
only when the mites are present.
The function of the webbing may con-
ceivably be to afford protection to the
spinning eriophyids. Though several
species of predaceous mites were found
in conjunction with the webbing, no
predation of Aculops mites happened to
be observed. Protection is more likely
against the washing effects of rains. The
anchoring function seems borne out by
the virtual non-establishment of webs on
leaves emerging after onset of the mon-
soon rains.
References Cited
Gooding, G. V., Jr., and W. W. Bing. 1970.
Serological identification of potato virus Y and
tobacco etch virus using immunodiffusion plates
containing sodium dodecyl sulfate. Phyto-
pathology 60: 1293 (Abstr.).
Keifer, H. H. 1975. Eriophyid Studies C-11.
California Dept. Agric., Bur. Entom., 24 pp.
. 1976. Eriophyid Studies C-12. California
Dept. Agric., Bur. Entom., 24 pp.
Purcifull, D. E., E. Hiebert, and J. G. McDonald.
1973. Immunochemical specificity of cytoplasmic
inclusions induced by viruses in the potato Y
group. Virology 55: 275-279.
Purcifull, D. E., T. A. Zitter, and E. Hiebert. 1975.
Morphology, host range, and serological relation-
ships of pepper mottle virus. Phytopathology
65: 559-562.
Shepard, J. F. 1972. Gel-diffusion methods for
the serological detection of potato viruses X, S,
and M. Montana Agric. Exp. Sta. Bulletin 662,
72 pp.
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Notes on Tadpoles as Prey for Naiads and Turtles
W. Ronald Heyer and Miriam H. Muedeking
Amphibians and Reptiles, Smithsonian Institution, Washington, D. C. 20560
Although there is a large literature on
predator-prey interaction theory, there
are still some specific interactions for
which there is little or no information.
Naiads and turtles are known predators
on tadpoles, but nothing is known con-
cerning feeding rates involved. In order
to gather some basic information on these
specific interactions, we ran some simple,
straightforward experiments while on
Barro Colorado Island, Canal Zone, in
July 1975.
Naiad-Tadpole Experiments
The purpose of the experiments was
to determine the maximum feeding rate
of naiads, using tadpoles as prey. All
experimental animals, plants and water
came from a cement pond in the living
compound built by A. S. Rand for his
studies on Physalaemus pustulosus.
Holding and experimental containers
were square or round plastic containers
approximately 9 cm across, filled with
pond water 4 cm deep. Large naiads
(Family Libellulidae, Orthemis sp. prob.
ferruginea) were isolated for 1 or 2 days
prior to introducing them to the prey.
Each experimental tray had | naiad, some
water weed (Hydrella), and a super-
abundance of prey, either 30 or SO indi-
viduals, depending on prey type. Three
types of prey were used: 30 small
Agalychnis callidryas tadpoles, 50 small
Physalaemus pustulosus tadpoles, or 30
large Physalaemus pustulosus tadpoles.
Experiments were run from 22-%4 to
26-%hr. Other projects did not allow
exact 24-hr experimental runs in all
cases. All tadpole larvae were well
within the size range on which the naiads
could feed. At the end of each experi-
ment, the naiad and remaining prey were
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
preserved together in a vial containing
10% formalin. Five replicates of small
Agalychnis, 10 replicates of small Phy-
salaemus, and 12 replicates of large
Physalaemus were run. In one of the
small Agalychnis runs, several tadpoles
died in handling; the results of this
particular run are not included in the
analyses.
In the laboratory, the following data
were taken from specimens in each
experimental vial: 1) the number of
tadpoles left after the experiment; 2) the
volume of the tadpoles left after the
experiment, 3) the volume of the naiad.
Volumes were determined by formalin
displacement in a 10-ml graduated cylin-
der. Excess surface moisture was re-
moved by paper towelling before volume
determination. From these data, the
following were determined: 1) the num-
ber of tadpoles consumed during the
experiment (initial number minus number
left), 2) the volume of tadpoles eaten per
predator adjusted to 24 h. The assump-
tion used in determing this last value
is that the sizes of the tadpoles consumed
were the same as the sizes of the tadpoles
left in each experiment. As post-hatch-
ling Agalychnia and large premeta-
morphic Physalaemus were used, the
size variances in experiments using these
prey were not great. The greatest size
variance was in the experiments run with
small Physalaemus as prey.
The data were analyzed using the
UCLA Biomedical 10V program (Dixon,
1974), general linear hypothesis without
and with a covariate, testing numbers
of prey and volumes of prey consumed
separately.
The results of the analysis testing kinds
of prey based on numbers of prey eaten
are presented in Table 1. There is a signif-
235
TABLE 1.—Analysis of number of prey types eaten with no covariate. Pl = Agal-
ychnis, P2 = Small Physalaemus, P3 = Large Physalaemus. SS = sums of squares,
DF = degrees of freedom, MS = mean squares, * = significant at the 5% level,
** — significant at the 1% level.
Source SS DF
Prey 221.86145 D,
Pil = ew 31.77779 1
IP = 15) SSA 1
PD = 13 221.79206 1
Error $17.94317 28
icant difference in the number eaten
among the 3 prey types and the difference
is between the number of small Physalae-
mus VS. large Physalaemus eaten.
The results of the analysis testing kinds
of prey based on volumes of prey eaten
are presented in Table 2. There are no
significant differences among the volumes
eaten of the 3 prey types.
Large naiads were purposely chosen to
minimize the variation in the experiments
due to predator differences. Predator-
prey size relationships are very important,
however (e.g. Heyer et al., 1975), so
the data were tested to see if the results
were affected by differences in sizes
among the predators. To test, volume of
predator was used as the size factor and
included as a covariate with the data as
analyzed in Tables 1 and 2. The results
with the covariate added are presented in
Tables 3 and 4. The results are exactly
the same as in Tables 1 and 2; size dif-
ferences among the predators used had
no effect on the experiments.
The average number of Agalychnis
consumed per naiad over 24 h is 5.7 with
an average volume of 0.038 ml/tadpole.
The average number of small Physalae-
mus consumed per naiad over 24h is
9.0 with an average volume of 0.027 ml/
tadpole. The average number of large
Physalaemus consumed per naiad over
24h is 2.63 with an average volume of
0.109 ml/tadpole. An individual naiad
consumed 0.77 of its volume in prey
tadpoles per 24-h on the average.
Turtle-Tadpole Experiment
A single 49.5-mm-carapace-length ju-
venile turtle, Chrysemys scripta, was
236
MS F
110.93072 4.92604*
ala) 1.41114
Pe S74 1eZS2on
221.79206 9.84900**
22.51926
found in Rand’s pond. After isolating
the turtle for 24h, it was placed in a
plastic container of the same size as used
in the naiad experiments, without water
weed, and with 30 large Physalaemus.
After 26-*%4 h, all of the tadpoles had been
killed and at least partially consumed.
The water was turbid. After isolating the
turtle for 24 h, it was placed in the bottom
of a plastic Chlorox bottle from which the
top half had been cut off. The bottle was
15 cm in diameter and water was placed
4 cm deep. Some Hydrella was added
along with 30 large Physalaemus. We
were interested in knowing if giving the
prey a better opportunity to hide from —
the predator would make a difference in
the results. After 26.5 h, only 1 tadpole
was left alive. The water was clear. The
turtle was isolated for another 24 h. The
experimental setup was the same as the
previous run except 100 large Physalae-
mus were added. After 27 h, 1 Physalae-
mus was left alive. The water was rela-
tively clear. The turtle was isolated for
48 h. The next experiment differed only
in adding 200 large Physalaemus. After
25-44 h, 71 Physalaemus were alive, but
the water was dark brown as in the first
run. As turtles are largely visual feeders,
TABLE 2.—Analysis of volume of prey types
eaten with no covariate. See Table 1 for explanation
of abbreviations.
Source SS DF MS F
Prey 0.08021 D. 0.04011 0.63027
Riese? 0.07498 1 0.07498 1.17833
Ei— P83 0.06235 1 0.06235 0.97984
[PD 128} 0.00173 1 0.00173 0.02726
Error 1.46360 23 0.06363
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
TABLE 3.—Analysis of number of prey types eaten with naiad volume as a covari-
ate. See Table 1 for explanation of abbreviations.
Source SS
Prey 211.99865
Ei 2 32.594 13
Pie P3 29.91784
Pa —P3 211.99650
Covariate 2.35026
Error $15.59291
the limits of the experimental design had
been reached.
Discussion
A model has been proposed recently
which attributed a limiting factor of tad-
pole diversity to fish predation (Heyer
et al., 1975). The same authors com-
mented that other vertebrate predators
may also control tadpole diversity through
completely eliminating tadpole popula-
tions in given ponds. Such invertebrate
predators as dragonfly larvae were con-
sidered not to be able to eliminate tadpole
populations, although tadpole popula-
tions could be markedly reduced. The
critical aspect is elimination, not reduc-
tion of tadpole populations.
Although Rand’s pond from which all
experimental animals were taken is
artificial, the assemblage of species in it
probably is not. For purposes of discus-
sion, then, only the species populations
in this pond will be examined. There are
two aspects to eliminating tadpole popu-
lations; eliminating the tadpoles from a
single clutch of eggs and eliminating the
total tadpole population, which would
result from 1 or more clutches of eggs.
The average of 16 Agalychnis egg clutches
TABLE 4.—Analysis of volume of prey types
eaten with naiad volume as a covariate. See Table 1
for explanation of abbreviations.
Source SS DF MS F
Prey 0.08164 y 0.04082 0.63759
mie= P2 0.08159 1 0.08159 1.27454
P= P3 0.03877 1 0.03877 0.60558
Er? = P3 0.01371 1 0.01371 0.21413
Covariate 0.05517 1 0.05517 0.86185
Error 1.40843 2D 0.06402
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
DF
N
MS F
M, 105 .99932 4.52292*
l 32.594 13 S907)
1 29.91784 1.27657
l 211.99650 9.04575**
1 2.35026 0.10028
2 23.43604
counted was 53.4; of 3 Physalaemus
nests counted, 216.7.
The turtle, Chrysemys scripta, could
possibly eliminate the tadpoles from a
clutch of Agalychnis eggs in about 0.5
day, and the tadpoles of a Physalaemus
clutch in somewhat more than 1 day. By
remaining in a pond for a few days,
Chrysemys scripta could theoretically
eliminate the tadpole population from the
pond, assuming moderate anuran repro-
ductive output. Whether turtles remove
entire tadpole populations in nature
remains to be determined, however.
There is at least one reason to believe
that turtles would not eliminate tadpoles.
Turtles are mobile feeders; as the tadpole
population is reduced, the energy spent
in capture becomes greater. There is
likely a point where the energy expendi-
ture per capture becomes so great that
the turtle switches to another prey, if
available. The experimental evidence
presented here suggests that turtles can
be effective tadpole predators, even if
turtles do not completely eliminate tad-
pole populations.
If the average consumption rates of the
large naiads are used together with aver-
age clutch size, it takes A) 9.4 large
naiad days to consume the small tadpoles
from a single Agalychnis clutch; B) 24.1
large naiad days to consume the tadpoles
from a single Physalaemus clutch if the
tadpoles are consumed when small; C)
82.4 large naiad days to consume the
tadpoles from a single Physalaemus
clutch if the tadpoles are consumed when
large. These are probably maximal rates,
as the experiments were designed to
saturate the predators with prey.
From these data, it would appear that
237
a small population of large naiads could
eliminate Agalychnis tadpoles from a
pond. The experiments did not take
habitat differences into account, how-
ever. The experimental trays were small
enough that the naiad could sample tad-
poles from the entire water volume, as
there was enough Hydrella in the trays
to allow this. In the pond from which
the experimental animals were taken,
the naiads were either sitting camouflaged
on the cement edge or in Hydrella mats.
The Agalychnis were in the open water;
the Physalaemus appeared to be every-
where. Thus, the naiads and Agalychnis
tadpoles were effectively spatially iso-
lated. Another factor contributing to the
likelihood that naiads would not eliminate
Agalychnis tadpoles from ponds relates
to size. Agalychnis hatchlings are large
and the tadpoles become much larger than
Physalaemus tadpoles. Large Agalychnis
tadpoles are too large for the size naiads
used in the experiments to feed upon
(also see Heyer et al., 1975). Thus, in
nature, we would not expect naiads to
regularly eliminate Agalychnis tadpoles
from ponds.
The Physalaemus larvae are always
within the size range of prey items for
the size of naiad used in the experiments,
and the tadpoles and naiads occur in the
same pond habitats. The ingestion rates
suggest that the Physalaemus tadpoles
would not be eliminated by naiads, how-
ever. The duration of the Physalaemus
larval stage probably does not exceed 30
days and small Physalaemus larvae
would grow to large larvae within 2 to 3
weeks. In terms of a clutch, then, even
with maximum naiad predation, some lar-
vae would avoid predation and become
large larvae; once the Physalaemus \ar-
vae are large, the rate of predation falls
markedly, such that some larvae would
make it through to metamorphosis.
The naiad evidence presented here,
while not conclusive, is consistent with
the hypothesis that under usual condi-
tions, naiads will reduce—not eliminate
—tadpole populations. This was cer-
tainly true in the pond from which the
experimental animals were taken. There
238
was a noticeably present naiad popula-
tion, many Agalychnis tadpoles and an
abundance of Physalaemus tadpoles.
Assuming that naiads were consuming
tadpoles in the pond, the tadpoles were
not eliminated; many made it through to
metamorphosis during the time we ob-
served the pond.
Under unusual conditions, when the
numbers of naiads per volume water is
greater than usual, and pond microhabitat
differences disappear, the data presented
here suggest that naiads could eliminate
tadpole populations. Such conditions
can occur when temporary ponds dry up
as have been reported from field situa-
tions (Heyer, 1973).
Another important factor to consider
is the nutritive value of tadpoles. Tad-
poles are feeding machines, and an un-
usually large part of the volume of a
tadpole is gut. The gut contents, usually
algae and diatoms, are not digestible by
many tadpole predators, so the total food
value of a tadpole to its predator is
effectively much less than of a similar
sized fish, for example (R. T. Lovell, |
pers. comm.). Thus, particularly for |
vertebrate predators, tadpoles may be
consumed only when they are very
abundant relative to other prey items.
The avoidance of tadpoles as prey
might involve a tast preference as the
gut contents of the tadpole may be
distasteful.
One aspect of the experiments invites
speculation. The results indicate that
naiads feed until they are full, irrespective
of the number of prey items it takes to
fill them. It would be interesting to know
the relative energy costs of naiads catch-
ing 9 small Physalaemus vs. 3 large
Physalaemus per day. There are two
energy costs to a naiad in consuming
prey: 1) the cost of discharing the catch-
ing apparatus and trapping the prey (fixed
energy cost due to the mechanism in-
volved), 2) the cost of manipulating the
struggling prey back into the mouth to
be eaten (variable cost). If the latter |
energy cost is the same for small and
large Physalaemus, then a naiad would |
clearly benefit energywise by concen-
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
trating on larger prey items. If large
struggling tadpoles take much more
energy to manipulate into the mouth than
small tadpoles, then a naiad would benefit
in an energy budget by concentrating on
smaller prey items. To our knowledge,
the relative energy budgets involved
in prey capture by naiads are unknown.
Acknowledgments
Oliver S. Flint and George R. Zug,
Smithsonian Institution, carefully read
the manuscript. Dr. Flint also identified
the naiads. Charles D. Roberts, Smith-
sonian Institution, provided statistical
analyses and interpretations of the data.
Susan Arnold took the laboratory data
and prepared the data for statistical
analysis. George Folkerts, Auburn Uni-
versity, discussed some of the results
with us and told us of the work of R. T.
Lovell. Laura and Elena Heyer assisted
with the experiments. Financial support
from the Environmental Sciences Pro-
gram, Smithsonian Institution, made the
study possible.
References Cited
Dixon, W. J. [ed.]. 1974. BMD Biomedical Com-
puter Programs. Univ. California Press, Berkeley.
773 pp.
Heyer, W. R. 1973. Ecological interactions of frog
larvae at a seasonal tropical location in Thailand.
J. Herpetology 7: 337-361.
,» R. W. McDiarmid, and D. L. Weigmann.
1975. Tadpoles, predation and pond habitats in
the tropics. Biotropica 7: 100-111.
Notched Teeth from the Texas Panhandle
P. Willey and D. H. Ubelaker
Department of Anthropology, University of Tennessee, Knoxville, 37916;
and Department of Anthropology, Smithsonian Institution,
Washington, D. C. 20560, respectively.
ABSTRACT
Mutilated human teeth from prehistoric North America have previously been
reported from relatively late prehistoric sites in areas of well-known Mesoamerican
influence. Recently 2 examples of probably filed teeth have been found in sites from
the Texas Panhandle, an area not known for Mesoamerican influence. In addition, the
skeletons could be considerably older than those previously reported, perhaps from
the Archaic period.
The presence in prehistoric Meso-
america of a wide-spread custom of tooth
mutilation involving various types of
notches and grooves has been known for
a long time and now is well documented
(Romero, 1970). However, not until
1944, when a series of 4 articles began
appearing in this Journal, was clear
evidence presented that the custom had
made its way into prehistoric America
north of Mexico. Although there was
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
an early mention of the finding of notched
teeth at Sikyatki Pueblo, Arizona (Saville
1913: 378, footnote 1), Campbell (1944)
was the first to describe the teeth in full.
The same year Stewart and Titterington
reported 1 labially grooved and several
occlusally notched teeth from Cahokia
and vicinity in Illinois. Additional exam-
ples were described later from Macon,
Georgia (Stewart and Titterington, 1946:
259—260), the Dickson Mound in Illinois
239
OKLAHOMA
NEW MEXICO
Lf
Gun Sight
ter *
Fig. 1.—Texas Panhandle showing the locations
of the Taylor Ranch Site and Gun Sight Shelter.
(Stewart and Titterington, 1946: 260-
261), the Rees Site near Cahokia, Illinois
(Holder and Stewart, 1958: 349-356),
and from Cahokia itself (Holder and
Stewart, 1958: 356). Stewart summarized
all these finds in his book (1973: 193),
noting that they all came from archeologi-
cal contexts, suggesting a late prehistoric
time period and substantial Mesoameri-
can influence.
As one might expect, the highly visible
anterior teeth are those most often modi-
fied. Among the specimens described in
the publications mentioned, the central
incisors are most common, the lateral
incisors next most common, and the
canines least common (actually only 1
has been reported). The mutilations thus
far reported are of the simplest of forms:
1 or more V-shaped notches filed into
the occlusal surface and/or a transverse
labial groove. The labial groove is easily
confused with defective enamel resulting
from hypoplasia.
Recently 2 Indian skeletons with
notched teeth were recovered through
the careful excavation of 2 different
burials in the Texas Panhandle, an area
with no other evidence of direct Meso-
american influence. In addition, both
discovery sites possibly date from the
Archaic Period, which, if confirmed,
240
would add considerably to the known
antiquity of the custom in North America.
Our purpose here is to present the
provenience, description, and implica-
tions of the new finds.
Taylor Ranch Burial
The Taylor Ranch Burial (Panhandle-
Plains Historical Museum Site A-1063;
Burial 1) was found about Christmas 1972
by the ranch-owner, Walter Taylor, 6 air
mi southwest of Quitaque, Texas (Fig.
1). Taylor and his daughter partially
excavated the burial in July 1973 and
then notified Dr. Jack T. Hughes, De-
partment of Geology and Anthropology,
West Texas State University, Canyon,
and Mr. Billy R. Harrison, Panhandle-
Plains Historical Museum. On July 27,
1973, Hughes and Harrison (Hughes’
field notes for that date filed with the
Panhandle-Plains Historical Museum)
were given the bones already removed
(left arm, leg, innominate, and scapula),
were guided to the burial location, and
were allowed to expose and remove the
rest of the burial. The bones were re-
moved in clumps which included the
dirt matrix and were transferred to West
Texas State University, where in No-
vember of 1974 they were processed by
a field archeology class under the direc-
tion of the first author. It was then that
the notched incisors were discovered by
Mr. Billy Pat Newman, a student in the
class. The skull and mandible were
shipped to the second author for inspec-
tion but were later returned and are now
housed in the Panhandle-Plains Historical
Museum.
According to Hughes (field notes),
the burial was exposed in the side of
a deep sinkhole (Fig. 2) in a colluvial
bench of North Pole Creek. The sinkhole
occurred where the colluvial bench
joined a bedrock cliff at the neck of a
long narrow meander, and in all proba-
bility the 40-yard-long sinkhole was
caused by underground drainage across
the neck of land. The bench consisted
of a compact light pink sand colluvium
which, as indicated by the sinkhole’s
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
profile, was at least 24.5 ft thick. The
skeleton was exposed in a vertical side
of the sink 12.5 ft from the bottom of
the hole, 12 ft from the top, and al-
though the pit was not clearly delineated,
the skeleton was most likely buried from
a surface 2.5 ft above the bottom of the
grave. Above the pit bottom 1.9 ft were
two large sandstone slabs, the most com-
mon rock in the area (Fig. 3), and at 2.5 ft
a smaller sandstone rock seemingly in-
dicated the surface from which the grave
was dug. The surface was vaguely
marked there and elsewhere in the
exposure by a line of differential erosion.
Both below and above the old surface,
the colluvium was massive, suggesting
rapid accumulation both before and after
the formation of the old, weathered
surface. However, this rapidly accumu-
lated colluvium does not rule out con-
siderable antiquity of the burial. Hughes
(personal communication) believes the
burial is probably Archaic, although this
Fig. 2.—Partially excavated Taylor Ranch
Burial in side of sinkhole. The skeleton is
approximately 12 ft from the top and 12 ft from the
bottom of the sink. View is to the southwest.
Photograph courtesy of Jack T. Hughes.
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Fig. 3.—Taylor Ranch Burial. Note the 2 large
sandstone slabs above the skeleton and above them
a line of differential erosion which apparently
indicates the surface from which the grave was
dug. View is south. Photograph courtesy of
Jack T. Hughes.
antiquity is difficult to prove due to the
lack of associated artifacts.
The skeleton was apparently placed in
a small oval-shaped, shallow pit, meas-
uring 2.25 ft east-west, at least 1.25 ft
north-south, and as noted above, probably
2.5 ft deep. The individual was lying
on its back, legs tightly flexed upward
and to the left, arms semi-flexed with the
hands near the pelvic region, head to the
west but facing southeast (Fig. 4). In
addition to the 3 sandstone rocks men-
tioned above, 5 burned sandstone cobbles
were on top of the chest and pelvis, a
Tecovas jasper flake was south (right) of
the pelvis, and several small shells
(Succinea?) and scattered charcoal flecks
occurred throughout the pit-fill. The
sandstone cobbles were likely intention-
ally interred with the person; the flake,
Shells, and charcoal may have been there
fortuitously. Other than the depth below
ground level, the burial is like many
other Indian interments from the area.
The bones of the Taylor Ranch Burial
are in a fair state of preservation; most
of the bone shafts are intact, but the
ends are commonly missing and none—
even those reconstructed—is complete.
241
Fig. 4.—Close-up of the Taylor Ranch Burial in situ. The skeleton is lying on its back, leg flexed
upward and to the left, head to the west but facing southeast. View is to the south. Photograph courtesy
of Jack T. Hughes.
All bones are stained pink, typical of
the effects of extended contact with the
red Triassic or Permian soils or soils
derived from either of these. Isolated
charcoal stains occur on 2 cervical
vertebrae, the greater trochanter of the
left femur, and the left fifth metatarsal.
Rather than being the marks of in situ
burning, the charcoal stains appear to
represent sites of contact with small char-
coal pieces in the soil since the marks
are small, homogeneously colored, and
do not penetrate to the interior can-
cellous bone.
The skull was recovered intact but
came apart during cleaning. It was
easily repaired with minimum warpage.
In addition to the skull and mandible,
most of the other major bones are
represented including parts of all major
limb bones (except the left humerus)
as well as many bones of the hands, feet,
chest, and pelvis. There are no indica-
tions that more than | person is present.
The skeletal remains suggest a female.
The pubic region, sciatic notch, femur
242
head diameter, and the general lack of
robusticity all support this identification.
There can also be little doubt con-
cerning the race of the individual. The
shovel-shaped incisors and flat face sug-
gest that the person was Mongoloid.
These morphological observations coupled
with inferences made from the archeo-
logic and geologic contexts indicate the
person was American Indian.
Age was estimated from the degree of
epiphyseal union, suture closure, pubic
symphysis change, and tooth wear. All
of the criteria indicate a person in the
16 to 22 yr age range with the exception
of Gilbert and McKern’s method for
female pubic symphysis aging, which
suggested a greater range but include the
years mentioned above. This last method
is most appropriate for aging older
females.
All teeth are present except the left
maxillary third molar and both mandibu-
lar third molars which appear to be con-
genitally missing. All teeth display some
crown loss due to attrition, especially the
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
first molars. Notches occur in the center
of the labial incisal edge of the mandibular
and maxillary central incisors (Figs. 5,
6). The notches are V-shaped, located
centrally in the maxillary incisors and
slightly right of center in the mandibular
incisors. In all cases the borders of the
notches are clear-cut and sharply defined.
The notches on the mandibular teeth are
slightly closer together than on the
maxillary teeth. Thus with the mandible
and maxilla in occlusion, the notches
do not exactly match. Also the paired
notches themselves do not correspond
in size. Both maxillary notches are
much wider than those of the mandible.
Originally the notches may have been
more apparent since the incisor crowns
have been reduced at least 1 millimeter
by attrition.
Burial From The Gun Sight Shelter
The Gun Sight Shelter, (Panhandle-
Plains Historical Museum Site A-1203),
located near Vega, Texas (Fig. 1), was
excavated by Mr. Billy Ray Thompson
of Amarillo, Texas. He is affiliated with
the Panhandle-Plains Historical Museum
in Canyon, Texas, and performed most
of the work with volunteer amateur
archeologists during the spring and
summer of 1974. The artifacts he col-
lected have been processed, and a report
is being prepared which will describe
the burial and its context more fully.
However, preliminary information indi-
cates that the shelter contains mostly
Archaic and NeolIndian cultural remains
and was inhabited between 1500 B.C. and
1400 A.D.
The skeletal parts were badly disturbed
by burrowing animals, with most of the
bones badly fragmented, but nearly all
major bones are present. From initial
impressions, the individual appears to be
an adult male.
Teeth present include from the mandi-
ble: incisors (4), right canine (1), right
premolars (2), and right molars (3); from
the maxilla: a central incisor (1), lateral
incisors (2), left canine (1), premolars (2),
and both first molars (2), for a total of
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Fig. 5.—Front view of the Taylor Ranch skull
and mandible showing the notched teeth. The
skull is not oriented in the Frankfort Plane.
18 teeth. Notches occur on the mandibu-
lar central incisors and right lateral in-
cisor (Fig. 7). The left central incisor
has the most pronounced notch, which is
V-shaped and extends from the labial
margin of the occlusal surface lingually
four-fifths of the diameter of the crown;
the notch is deepest on the labial aspect
from where it tapers lingually. The altera-
tion on each of the other 2 mandibular
incisors consists of little more than a
slight groove in the middle of the labial
half of the occlusal surface.Similarly, a
slight indentation occurs on the left
labial edge of the occlusal surface of
what may be a left lateral maxillary
incisor.
All of the teeth display extensive
crown reduction due to attrition. In
particular the mandibular teeth display-
ing the grooves have no crowns remain-
ing whatsoever, which is not uncommon
in middle-aged adult Indians from the
region. The grooves occur in the
secondary dentine and root stumps.
Another sort of alteration occurs on
243
Fig. 6.—Close-up of the notched teeth of the Taylor Ranch Burial. Note that only 1 set of notches
can match when held in a single position and that the maxillary notches are wider than those of the
mandible.
the right first maxillary molar, which
has an interproximal groove on the
buccal-distal corner at the junction of
the crown and root.
As in the case of the Taylor Ranch
specimen, the mandible and teeth of the
Gun Sight Shelter specimen were shipped
to the second author and subsequently
returned to the Panhandle-Plains Histori-
cal Museum.
Discussion
As mentioned before, there have been
less than a dozen mutilated or possibly
mutilated teeth reported from North
244
America. These teeth come from archeo-
logical contexts suggesting late time
periods and areas of considerable Meso-
american influence—late Puebloan from
Arizona and Mississippian from Illinois
and Georgia. The tooth modifications re-
ported fall into 2 categories: namely,
labial grooves and occlusal notches.
Putting aside the question of the labial
grooves and their possibly hypoplastic
origins, the notched teeth can be divided
into those with single notching and those
with multiple. The Texas examples, of
course, fall in the former category and
are most similar to those from the Sikyatki
Site in Arizona, which, perhaps signif-
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Fig. 7.—Gun Sight Shelter mandibular fragment with 3 notched teeth: namely, right
lateral and both central incisors. The mandible has been oriented to emphasize the notches.
icantly, is the geographically closest of
the sites with reported mutilations.
There are essentially 2 methods by
which the notched teeth from the Texas
Panhandle could have been produced.
One way is by purposeful filing pre-
sumably to alter the tooth form in a
culturally prescribed manner. The other
way is by accident. In this latter process,
the teeth may have been used as tools,
perhaps as a vise, to modify other objects
that in turn altered the teeth themselves.
The notched teeth from the Texas
Panhandle appear to result from inten-
‘tional mutilation rather than the use of
teeth as tools. In the case of the Taylor
Ranch Burial, the sharp, clear-cut borders
of the notches as well as the lack of
_ juxtaposition between the mandibular
- and maxillary notches argue for mutila-
tion. Although the Gun Sight Shelter
notches are rounded and more groove-
like than those of the Taylor Ranch
Burial, these modifications can be ex-
of what was formerly a much larger notch
before attrition destroyed the crown.
Mike the) notched teeth irom the
Sikyatki Site, the Texas examples are
much less elaborate than most examples
reported by Romero (1970) from Mexico
or even the few reported examples from
the eastern U. S. Some of the other U. S.
examples involve mutiple notches accom-
panied by labial grooves. Of course, the
Texas examples once may have been
more elaborate, before attrition de-
stroyed most of the crowns.
The Texas examples appear to expand
both the documented geographical and
temporal ranges of notching in the
United States. The geographical occur-
rence is somewhat surprising, since the
Texas Panhandle lacks other evidence
of significant direct Mesoamerican con-
tact, although Southwestern influences
may be present. The temporal extension
is even more surprising, since all other
examples of notching in the United
_ plained by marked attrition. The notches
_ probably represent the most apical aspect
States occur relatively late. The eastern
examples are all from Mississippian sites,
__ J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976 245
dating no earlier than A.D. 700 and
probably much later. The Arizona speci-
men dates very late, possibly into the
historic period. As stated earlier, the
Texas examples may be considerably
earlier, possibly even Archaic. This new
evidence suggests that the practice of
notching in prehistoric North America
may have had a considerably greater
geographical and temporal range than
previously suspected.
Acknowledgements
We wish to thank Billy R. Harrison,
Jack T. Hughes, and Billy Ray Thomp-
son for making their unpublished data
available; Jack T. Hughes and David
Hughes for the field photographs of the
Taylor Ranch Burial; Waldo R. Wedel
and T. D. Stewart for encouraging our
efforts; Stella Willey for the map and
paste-up work; and Becky Tarwater for
typing one of the manuscript drafts.
References Cited
Campbell, T. D. 1944. The dental condition of a
skull from the Sikyatki Site, Arizona. J. Wash.
Acad. Sci. 34(10): 321-322.
Holder, Preston, and T. D. Stewart. 1958. A
complete find of filed teeth from the Cahokia
Mounds in Illinois. J. Wash. Acad. Sci. 48(11):
349-357.
Romero, Javier. 1970. Dental mutilation,trephina-
tion and cranial deformation. In T. D. Stewart
(ed.), Handbook of Middle American Indians:
Vol. 9 Physical Anthropology, pp. 50-67.
University of Texas Press, Austin.
Saville, Marshall H. 1913. Precolumbian decoration
of the teeth in Ecuador with some account of
the occurrence of the custom in other parts
of North and South America. Amer. Anthropol.
15: 377-394.
Stewart T. D. 1946. More filed teeth from the
United States. J. Wash. Acad. Sci. 36(8):
259-261.
. 1973. The People of America. Scribner’s
Sons, 261 pp.
Stewart, T. D., and P. F. Titterington. 1944.
Filed Indian teeth from Illinois. J. Wash.
Acad. Sci. 34(10): 317-321.
ANNOUNCEMENT
WASHINGTON OPERATIONS RESEARCH COUNCIL
Wednesday, Jan. 19, 1977
‘*Planning and Evaluation in the Consumer
Product Safety Commission.’’ Joann Langston, Consumer Product
Safety Comm.
Wednesday, Feb. 9, 1977
Wednesday, March 9, 1977
‘*Social Science Directions in the Current
Administration.’ Arthur Spindler.
‘‘Analysis of the Paperwork Flow in the
Government.’’ Warren Buhler, Staff Director, President’s Commission
to Reduce the Flow of Paperwork.
April 18-19, 1977 Annual Symposium. ‘‘Natural Resources Policy.”’
Wednesday, May 11, 1977 Annual Banquet.
All meetings will be held at the Center for Naval Analyses, 7th floor
auditorium, 1401 Wilson Blvd., Arlington (Rosslyn) at 8:00 p.m.
246
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
ACADEMY AFFAIRS
BOARD OF MANAGERS MEETING NOTES
February 25, 1976
The 630th Meeting was called to order
at 8:10 p.m. by President Abraham in
the Conference Room of the Lee Build-
ing at FASEB. He introduced the officers
for 1975-76: Dr. Florence H. Forziati,
President-elect; Dr. Alfred Weissler,
Secretary; and Dr. Richard H. Foote,
Treasurer.
Treasurer.—Dr. Foote presented the
Treasurer's report for 1975, which
showed that income was about $6000
greater than expenditures. Although the
investment income was lower than in
1974, the value of capital assets at
year-end was $59,934.15, a substantial
increase from $43,810.85 in 1974. The
1975 report was accepted on a motion
by Dr. Robbins, seconded by Dr.
Weissler. Treasurer Foote also presented
the proposed budget for 1976, which esti-
mates income at $34,319 and expendi-
tures at $33,815. The budget was ap-
proved unanimously, on a motion by
Dr. Morris, seconded by Dr. Rowen.
Investments.—The possibility of in-
creasing the Academy’s investment in-
come was discussed in a presentation by
Mr. George Mitchell of the Washington
office of Moseley, Hallgarten and Esta-
brook, Inc. Mr. Mitchell noted that our
current return is less than 4% on our
investments in stock mutual funds; this
could be more than doubled by switching
into a capital bond fund. After a general
discussion on the need for balancing cur-
rent income against capital appreciation
prospects, President Abraham appointed
an ad hoc Committee, with Dr. Foote as
chairman, to consider the matter further.
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Divisional Structure. —President
Abraham pointed out the need to activate
the new divisional structure of the
Academy by having the appropriate
society delegates meet to elect a chair-
man for each Division. In order to ac-
complish this, he appointed the following
temporary chairmen: Dr. James F. Goff
for Physical Sciences and Mathematics,
Dr. Mary Louise Robbins for Life
Sciences, and Grover C. Sherlin for
Engineering.
Journal.—Dr. Foote reported that it
has finally become unavoidable to levy a
page charge of $25, which is modest as
compared with other journals. Sym-
posium IV will be published as the March
1976 issue of the Journal.
Policy Planning.—Dr. Alphonse
Forziati presented a written committee
report, and discussed one of the items
relating to a change of the Academy’s
name to ‘‘Washington Academy of Sci-
ences and Engineering.’’ The Board ex-
pressed favorable sentiment towards
such a change, by a straw vote of 9 to 4.
The Bylaws committee will be asked to
prepare the necessary amendments to
charter and Bylaws, which will then be
submitted to the Academy membership
for a vote.
Meetings. —Dr. Goff reported that the
average attendance at the montly meet-
ings this year has been 64. He attributed
this success to the selection of a good
variety of topics.
Public Information. Dr. Rowen ex-
pressed the hope that the new Divisions
247
will help in publicizing the meetings and
other activities of the Academy. He
also reported on recent discussions
of the societal interactions with science
and engineering, which were held by
the Science, Engineering, and Society
Committee.
Grants-in-Aid. An announcement was
made of the availability of approximately
$639 to aid student projects in mathe-
matics and science. It was also noted that
the JBSEE is preparing a new list of
ideas for student science projects.
Membership. Dr. Florence Forziati
presented 4 nominees for fellowship: Dr.
S. H. Durrani, Dr. Lloyd Knutson, Dr.
K. G. Powers, and Dr. Rogert H. Law-
son. All 4, plus Dr. William K. Blake who
is the new delegate of the D. C. Chapter
of the Acoustical Society of America,
were unanimously approved as Fellows.
Scientific Achievement.—Dr. Kelso
B. Morris thanked Ms. Ostaggi and the
panel chairpersons for their labors in
selecting the 1975 Scientific Achievement
Award winners: Biological Sciences,
Wayne A. Hendrickson, NRL; Engineer-
ing Sciences, Gerard V. Trunk, NRL;
Behavioral Sciences, Julius E. Uhlaner,
US Army Res. Inst.; Mathematics,
Charles R. Johnson, Univ. of Md.; Physi-
cal Sciences, William K. Rose; Teaching
of Science, Peggy Dixon, Montgomery
College; Lamberton Award for Teaching
of High School Science, Edythe G.
Durie. The report was approved on a
motion by Dr. Alphonse Forziati,
seconded by Dr. Robbins. (See JWAS,
Vol. 66, No. 2, pp. 152=—156. ==Ba))
Tellers. —Mr. Buras reported the re-
sults of the recent election for 1976—77
officers, as follows: Richard H. Foote,
President-elect; Nelson W. Rupp, Secre-
tary; Mary H. Aldridge, Treasurer; Rita
R. Colwell and Grover C. Sherlin,
Managers-at-Large.
In addition, the change in bylaws and
the affiliation of the Washington Paint
Technical Group were approved by a
large majority. Mr. Buras recommended
that future ballots use a simple plurality
system, and also only one side of the
paper because some members fail to turn
it over. The report was approved unani-
mously, upon a motion by Dr. Franz,
and seconded by Dr. Robbins.
New Business.—Photographs of past
presidents of the Academy should be
preserved for the future, Dr. Robbins
suggested. It was decided at least to main-
tain a file of such photographs, with con-
sideration later on a public display.
Dr. Wagner advocated a greater ex-
change of meeting notices among the
Academy’s affiliated societies.
Dr. Argauer noted that the Insecticide
Society of Washington had recently held
its 300th meeting, and suggested that
brief historical accounts of the affiliated
societies are suitable for publication in
the Journal of the Academy.
The meeting was adjourned at 10:35
p.m.—Alfred Weissler, Secretary.
NEW FELLOWS
Paul G. Campbell, National Bureau of
Standards, Sup. Res. Chemist, in recog-
nition of his contributions to organic
chemistry and in particular to his publi-
cations on the photo-oxidation of asphalt
and organic coatings. Sponsors: Florence
H. Forziati, Alphonse F. Forziati.
Shung-Chang Jong, Head, Mycology
Dept., American Type Culture Collec-
248
tion, Rockville, Md., in recognition of his
outstanding work in mycology. Spon-
sors: Rita R. Colwell, Richard H. Foote.
Robert B. Leachman, Special As-
sistant, Nuclear Regulatory Commission,
Wash., D. C., in recognition of his con-
tribution to physics, and in particular
his researches in nuclear fission and
heavy-ion physics, and on safegards
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
ee EEE
against misuse of nuclear materials.
Sponsors: George Abraham, Florence
H. Forziati.
Howard Lessoff, Branch Head, Naval
Res. Lab., in recognition of his activities
in solid state materials including magnetic
memory materials, basic spin wave
spectra interpretation and fundamental
understanding of electronic materials.
Sponsors: George Abraham, Emanuel
Brancato.
Cyril Ponnamperuma, Professor of
Chemistry; Director, Lab. of Chemical
Evolution, Univ. of Md., in recognition
of his extensive research on the chem-
istry of the origins of life. Sponsors:
James F. Goff, Bradley F. Bennett.
Harrell Leroy Strimple, Curator & Re-
search Investigator, Geology Dept.,
Univ. of Iowa, in recognition of his con-
tributions to invertebrate paleontology,
chiefly the Crinoidea. Sponsors: Flor-
ence H. Forziati, Alphonse F. Forziati.
John D. Walker, Microbial Ecologist,
Environmental Technology Ctr., Balti-
more, Md., in recognition of his outstand-
ing scientific work in microbial ecology.
Sponsors: R. R. Colwell, Richard H.
Foote.
Marvin H. White, Advisory Engineer,
Westinghouse Electric Corp., Baltimore,
Md., in recognition of pioneering contri-
butions to the theory and experimental
development of charge coupled electron
devices and imaging sensors. Sponsors:
Arthur S. Jensen, George Abraham.
Sanford C. Adler, President, Manage-
ment Factors Organization, McLean,
VA., in recognition of his contribution to
operations research, and in particular the
application of governmental resources in
the solution of problems relating to health
and safety. Sponsors: Jean K. Boek,
Joan R. Rosenblatt.
George E. Deal, NBS Operations Re-
search analyst, in recognition of his
contributions to the field of operations
research and of his research, leadership,
practice, and teaching in the area of
management. Sponsors: John W. Rowen,
James E. Fearn, Grover C. Sherlin.
SCIENTISTS IN THE NEWS
Contributions in this section of your Journal are earnestly solicited.
They should be typed double-spaced and sent to the Editor three
months preceeding the issue for which they are intended.
NATIONAL BUREAU OF STANDARDS
J. J. Diamond, Chief, Law Enforce-
ment Standards Laboratory, NBS, has
received the Department of Commerce
Silver Medal Award for valuable contri-
butions to the Nation’s law enforcement
officials by developing law enforcement
equipment standards. He is a 1937
graduate of Brooklyn College, Brooklyn,
NY.
DEPARTMENT OF THE ARMY
Howard S. Jones, Jr. has been given
a Meritorious Civilian Service Award
for his productive microwave antenna re-
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
search. This second highest civilian
award was presented to him for his im-
portant technical accomplishments and
major improvements in a variety of
Army weapon antennas for radar re-
lated systems.
Dr. Jones is the Chief of the Micro-
wave Branch 150, at the US Army Harry
Diamond Laboratories (HDL) Adelphi,
MD. He is recognized nationally and
internationally as an expert in the micro-
wave field specializing in microwave
devices and antenna arrays. His educa-
tional background includes B.S. and
D. Sc. degrees from Va. Union Uni-
versity, Richmond, VA, certificate in
249
Howard S. Jones, Jr.
Engineering, Howard University,
M.S.E.E. Buchnell University, Lewis-
burg, PA, plus other graduate work in
Math, Physics and Engineering. He also
completed the residential Executive
Education program at the Federal Execu-
tive Institute, Charlottesville, VA.
In 1972 he was the recipient of the
Secretary of the Army’s Research and
Study Fellowship award, and the inven-
tor of the year (HDL) award, cited for
his numerous contributions that have
advanced the antenna state-of-the-art
while providing solutions to critical
antenna problem areas of modern
weapon systems. He has also received
several other awards and citations dur-
ing his career, among which is included
the Army Research and Development
Achievement Award in 1975.
Early this year Dr. Jones was named
to the Thirty-Ninth Edition of Who’s
Who in America for his microwave con-
tributions that have bettered contem-
porary society.
He has served as a technical Consul-
tant to government agencies and private
industry, and was an assistant professor
at Howard University’s School of En-
250
gineering for several years. Other ac-
complishments include more than 30
technical reports, numerous oral presen-
tations and publications in the Scientific
Literature. He has received 24 US
patents relating to microwave antennas,
devices and design techniques.
Dr. Jones holds FELLOW status in the
Institute of Electrical and Electronic
Engineers (IEEE), American Associa-
tion for the Advancement of Science
(AAAS), and the Washington Academy
of Sciences (WAS). He is a member of
the Antenna and Propagation Society,
the Microwave Theory and Techniques
Society, and a registered professional
engineer in the District of Columbia.
IEEE
F. L. Hermach of the Electricity Divi-
sion has received the 1976 Morris E.
Leeds Awards of the IEEE for outstand-
ing contributions to the field of electrical
measurements. The award, consisting of
a certificate and $1,000., was presented
on June 28, 1976 at the Conference. on
Precision Electromagnetic Measure-
ments in Boulder, Colorado.
The award, one of the most prestigious
in its field, was given in recognition
of Mr. Hermach’s research and develop-
ment of extremely accurate ac-dc trans-
fer standards and for his outstanding
services on standards committees. All ac
voltage and current measurements de-
pend on these transfer standards or
comparators, which relate the ac quantity
to the basic dc standards at NBS. In his
37 years at the Bureau Mr. Hermach has
developed and verified new forms of
comparators, with greatly increased ac-
curacy and range. He has also repre-
sented NBS on major standards-writing
committees on electrical measurements
and on hazards from electricity.
SOCIETY OF COSMETIC CHEMISTS
Alfred Weissler of Chevy Chase, Md.
has been installed as president of the
Mid-Atlantic chapter of the Society of
Cosmetic Chemists for 1977. He has
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
served previously as president of the
Chemical Society of Washington and
president of the Washington chapter of
the Acoustical Society of America.
NAVAL RESEARCH LABORATORY
Jerome Karle, Chief Scientist of the
Laboratory for Structure of Matter at the
Naval Research Laboratory (NRL) here,
has been elected a member of the Na-
tional Academy of Sciences (NAS) and
also was named recipient of the 1976
Captain Dexter Conrad Award for Scien-
tific Achievement . . . both within one
week.
Dr. Karle is the fourth NRL member to
be elected to the NAS, considered one
of the highest honors that can be ac-
corded to an American scientist or
engineer. The other NRL members are:
Drs. Herbert Friedman, Richard Tousey,
and Samuel Collins.
NAS elected Dr. Karle and 74 other
new members to the society last month
in recognition of their distinguished and
continuing achievements in original re-
search. Their names were announced at
the business session of the 133rd annual
meeting of NAS April 27.
The Academy, a private organization
established in 1863 by a Congressional
Act of Incorporation signed by President
Lincoln, serves as official advisor to the
federal government, upon request, in any
matter of science or technology.
The Captain Robert Dexter Conrad
Award for Scientific Achievement is con-
sidered the highest recognition the De-
partment of the Navy can bestow on any
of its scientists engaged in research and
development for the Department.
The Chief of Naval Research, Rear
Admiral R. K. Geiger, in a letter to Dr.
Karle concerning the award, said *‘ Your
distinguished contributions in the study
of the structure of matter in vapor,
crystalline and amorphous states fully
merit this recognition. Your pioneering
efforts have advanced the scientific pres-
tige of the Navy and the Nation.”’
Dr. Karle received the Navy’s Dis-
tinguished Civilian Service Award, the
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Dr. Jerome Karle
highest Navy award available to civilian
employees, in 1968 for his ‘‘pioneering
advances, both theoretical and experi-
mental, and for his leadership in the
fields of the structure analysis of matter
by electron, x-ray, and neutron diffrac-
tion.’’ His work made it possible to study
the structures of a large variety of ma-
terials of interest to the Navy.
For the past 34 years, including almost
32 at NRL, Dr. Karle has conducted theo-
retical and experimental research in elec-
tron diffraction, x-ray diffraction, and
neutron diffraction as they pertain to
structural analysis of matter. With these
three distinct but related methods, scien-
tists delve into the infinitesimal world of
molecules and crystals in search of inter-
atomic distances and atomic arrange-
ments. This knowledge contributes to
fundamental progress in science in such
fields as organic and biological chemistry,
geology,and solid state physics.
An occasional collaborator in Dr.
Karle’s work is his wife, Dr. Isabella
Karle, also a noted scientist, recently
251
honored with the Garvan Medal of the
American Chemical Society and an
honorary Doctor of Science degree from
the University of Michigan. They have
collaborated on identifying the chemical
nature and solving the three-dimensional
structures of a number of highly active
substances of interest to physiology and
medicine.
A native of New York City, Dr. Karle
holds degrees from City College of New
York (BS—1937), Harvard University
(MA— 1938), and the University of
Michigan (MS and PhD— 1944). Before
joining the NRL staff in 1944, he had been
associated with the Manhattan Project
and had done contract work for NRL at
the University of Michigan, where he also
taught.
In 1968, Dr. Karle was named to the
Chair of Science for the Structure of
Matter at NRL, which was created in
recognition of his distinguished scientific
service. In 1970 he and his wife shared
the Hillebrand Award of the Chemical
Society of Washington.
252
Dr. Karle has authored or coauthored
over 150 manuscripts for technical
journals. He is a Fellow of the American
Physical Society and the Washington
Academy of Sciences. His membership in
professional societies includes the
American Mathematical Society, Amer-
ican Chemical Society, American Asso-
ciation for the Advancement of Science,
American Crystallographic Association,
and the Philosophical Society of Wash-
ington. He is a past-president of the
American Crystallographic Association
and is currently a consultant to the Na-
tional Science Foundation. He is also a
member of the American Heritage
Society and the National Society of
Literature and the Arts.
The Karles live in Falls Church, VA.
They have three daughters, Madeleine,
Jean, and Louise. Madeleine is a geology
major at Virginia Polytechnic Institute
and State University, and Jean, Louise
and Louise’s husband, Jonathan Hanson,
all have earned PhD degrees in chemis-
try.
J. WASH. ACAD. SCI., VOL. 66, NO. 4, 1976
Cte, ae RD
He
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D2w23
VOLUME 67
Number 1
| J Our nal of the MARCH, 1977
WASHINGTON
ACADEMY .-.SCIENCES
Issued Quarterly
at Washington, D.C.
=U
CONTENTS
Features:
DAVID M. SMITH: The Scientific Basis for Timber Harvesting Practices . 3
ELAINE G. SHAFRIN, et al.: Washington Junior Academy of Sciences—
ShiistinaswCOnVenmlOnm 1976) iia. once ee loess cece cee webs ee wees 12
Review:
MAY INSCOE: Chemical Communication in Insects .................05. 16
Research Reports:
JOHN M. HACKNEY and EDWARD M. BARROWS: Biological Notes on
Stenodynerus microstictus (Hymenoptera: Eumenidae) .............. 34
EDSON J. HAMBLETON: A Review of Pseudorhizoecus Green, With a
Description of a Related New Genus (Homoptera: Pseudococcidae) ... 38
ROBERT D. GORDON and O. L. CARTWRIGHT: Four New Species of
Aegialia (Coleoptera: Scarabaeidae) From California and Nevada Sand
IDUANES 5 co bo 6 Hels casi Oo FIGARO) OUI NES CoCin at sania tar 42
Academy Affairs:
he IPSIIOWYS ua 6 ga ob Sih tea eS REDE nS, ler Suen a en a oe 49
RePOmeoleme lens OmmMiltee . . 5 vances ccc ca eee se behea se cece ee ee bw eles ee 49
SEEMS. UMS Sa ee a eae 50
Obituary
Derik: G., RD oo oko ee ee ee 51
a menees, Ammouncements ...............0.. foc cece cee eee eee eee eee D5?
Washington Academy of Sciences
EXECUTIVE COMMITTEE
President
Florence H. Forziati
President-Elect
Richard H. Foote
Secretary
Nelson W. Rupp
a .
Treasurer
Mary H. Aldridge
Members at Large
a a
Founded in 1898
The Journal
This journal, the official organ of the Washington Aca-
demy of Sciences, publishes historical articles, critical
reviews, and scholarly scientific articles; proceedings
of meetings of the Academy and its Board of Mana-
gers; and other items of interest to Academy members.
The Journal appears four times a year (March, June,
September, and December)—the September issue
contains a directory of the Academy membership.
Subscription Rates
Members, fellows, and patrons in good standing re-
ceive the Journal without charge. Subscriptions are ~
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vance. Payment must be made in U.S. currency at the
following rates:
George Abraham U.S. and Canada....... $15.00
. Foreign ....354.-ee 16.50
Grover C. Sherlin Single Copy Price ...... 5.00 |
Single-copy price for Vol. 66, No. 1 (March, 1976) |
BOARD OF MANAGERS is $15.00.
All delegates of affiliated Back Issues
Societies (see facing page) Obtainable from the Academy office (address at bot-
tom of opposite column): Proceedings: Vols. 1-13
(1898-1910) Index: To Vols. 1-13 of the Proceedings
EDITOR and Vols. 1-40 of the Journal Journal: Back issues,
volumes, and sets (Vols. 1-62, 1911-1972) and all cur- |
Richard H. Foote rent issues.
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lowed because of failure to notify the Academy of a |
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Published quarterly in March, June, September, and December of each year by the
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DELEGATES TO THE WASHINGTON ACADEMY OF SCIENCES,
REPRESENTING THE LOCAL AFFILIATED SOCIETIES
Peep nied; SOCIeLy (Of WASMINGLOM 5. oe ei ots ste Sdlo.6 Sis Abi S 4 Os doa abla Se ooo owas James F. Goff
Peeepelnnicall Socicty of Washington ...).5.55..6se.cdve vedas bei wec bats ews snes Jean K. Boek
MRR SO CICIV Ol VV ASIMNOLONE 6.2) as fants Oh) So Sx nara Sai ds esis ab ods bea ell ooee euc eboe Inactive
ie eee USO GCICEV Ol VV ASMINOTON) | 2. hor. s hae dene s 22 Fas vie boa Sosee ease eee scene Mary H. Aldridge
EemnaiGeieal Society Of WaSRINGION . 2 66. os bk oe sce seen dc see deeeetuewsas Maynard Ramsay
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Bemncion electrical and Electronics Engineers ........7....5..0..00cbeeecseccces George Abraham
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(9 SESE EEE DCC WSU? LOIRE 1 SNS SO ee re Pe ere ee Glen W. Wensch
imemational Association of Dental Research ...:...5....0.00ccc ccc eceeeece William V. Loebenstein
mmerican Institute of Aeronautics and Astronautics ........0. 0.2.2 e cece cee eeees Franklin Ross
Eee tee IE OTOOPICA eSOCICLY: 6.) lo. oe Dee ic sec were he oUt BW ode Denese e's A. James Wagner
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Delegates continue in office until new selections are made by the representative societies.
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977 1
ANNOUNCEMENT
BELTSVILLE SYMPOSIUM II: BIOSYSTEMATICS IN AGRICULTURE
BELTSVILLE AGRICULTURAL RESEARCH CENTER
BELTSVILLE, MARYLAND
MAY 9-11, 1977
In 5 symposium sessions leading investigators will lecture or engage
in panel discussions on the role that biosystematics has in agriculture.
Main topics will include new techniques, taxonomic theories, uses of
taxonomic and biosystematic data, especially predictive applications,
and the planning and direction of biosystematic research. In addition,
a poster session and mixer is scheduled for the evening of May 9.
Manned displays at the mixer should generate valuable discussion.
For further information, send lower portion of this notice to:
Dr. James A. Duke
Publicity Committee, BARC Symposium II
Plant Taxonomy Laboratory
Room 117, Bldg. 001, BARC West, USDA
Beltsville, Maryland 20705 U.S.A.
BELTSVILLE SYMPOSIUM II: BIOSYSTEMATICS
IN AGRICULTURE
Please send further information on the Symposium to:
NAME
ADDRESS
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
Oe Ne ees
FEATURES
The Scientific Basis for Timber Harvesting Practices!
David M. Smith
Professor of Silviculture, Yale University School of Forestry
and Environmental Studies, New Haven, Connecticut 06511
ABSTRACT
Silviculture, the applied ecology of forestry, is fundamentally a planned simulation
of the seemingly destructive disturbances, small or large, gentle or severe, which have in
nature created kinds of forest vegetation now regarded as desirable for human needs.
Silviculture is the part of forestry that is
the applied science of growing stands of
trees. Trees have to live outdoors
through winter and summer, during dry
years and wet, usually on poor land
unsuitable for agriculture; society also
prices wood and other benefits at a low
rate; therefore, it has always been neces-
sary for foresters to work very closely
with rather than against natural proc-
esses. As a result, silviculture became a
form of applied ecology even before the
word was coined by a German scientist
during the last century.
The basic objective of silviculture,
in any given place, is to create a certain
desirable kind of vegetational develop-
ment. The fundamental analytical proce-
dure is to determine the processes that
created this in nature and then to sim-
ulate them directly or indirectly. The
astonishingly paradoxical point of all this
is that the ultimately constructive guiding
_ force in replacing old with new or even
_ with steering the development of estab-
' Presented at a joint meeting of the Washington
Academy of Sciences and the Washington Section,
Society of American Foresters, Arlington, Va.
_ November 18, 1976.
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
lished vegetation is lethally destructive
disturbance.
It was said long ago and probably ina
language other than English that the
forest is built with the wise use of the axe,
the same tool with which it can be wit-
lessly destroyed. This remains at least
figuratively true even though the number
of lethal constructive weapons has
increased. Fire (Fig. 1) and grazing ani-
mals probably came before the stone axe
in human manipulation of forest vege-
tation.
Let me attempt to indicate to you why
the silvicultural guidance of the estab-
lishment and growth of forests has to de-
pend on the judicious killing of trees and
other components of the vegetation. The
killing may be of single individuals or of
both large and small patches thereof.
In a certain, somewhat academic sense,
the question of whether the killing is or is
not done by harvesting trees for useful
products is rather incidental. The fact
that this mode of tree killing can pay the
costs and yield a profit is immensely
advantageous; however, the wise long-
term management of a picnic grove would
necessitate killing some trees. We might
well do it whether anyone ever used
3
wood or not. If we can sell the wood, the
net cost can be very substantially re-
duced.
Tree killing is the main silvicultural
tool because forest vegetation typically
fills all of the available growing space and
cannot be changed or guided in its de-
velopment without creating vacancies.
Vegetation in general, and that of woody
perennials in particular, hungrily expands
its foliar cover and roots to fill all of the
physiologically inhabitable space above
and below ground. The occupancy soon
becomes so complete that nothing new
can be added unless some growing
space is made vacant by killing some-
thing. Ina more subtle way, the growth of
one established plant can be enhanced by
killing a competing neighbor. This kind of
partial disturbance would merely speed
natural development if the favored plant
would have ultimately overgrown and
shaded out the one that’s artificially
killed; however, if nature would have
caused an opposite outcome, the partial
disturbance could somewhat alter the
course of development.
Any kind of vegetation tends to fill the
growing space. With forests, it is simply
more complete and more obvious. The
phenomenon of the perennial woody
stem is the most efficient terrestrial de-
vice for arranging energy-gathering
foliage such that it is dispersed in depth in
a transparent medium. Suspensions of
floating algae waste little or nothing on
supportive stems, but the medium is less
translucent and there is no vertical
conductive mechanism to take care of
moving chemical nutrients upward.
Water supply is something of a problem
on land. In fact, forests with a closed
foliar canopy exist only where there is
plenty of water. Where water is in short
supply but still sufficient for some trees to
exist, their root systems often fill the
whole soil stratum but the water that they
pick up is sufficient to support only an
incomplete foliar canopy.
I should underscore the point that the
trees grow to fill the available growing
space but not to use up all the growth-
- supporting factors. If they used all the
4
growth factors, there would be no water
left for stream flow; everything but the
green light would be used and things
beneath the forest would all look green.
Absolute shortages of a given essential
factor or seasonal shortages limit the
capacity to use others. A phosphorus
shortage might limit the amount of leafy
photosynthetic apparatus and thus the
amount of leaf tissue to transpire water;
this would in turn release more water to
stream flow. One manifestation of sea-
sonal shortages with temporary surpluses
is the development of understory vege-
tation with short annual cycles of active
growth.
The beautiful spring flora of the eastern
deciduous or hardwood forest is one of
the classic manifestations of this; the
spring flowers can burgeon to take advan-
tage of heat, light, and water faster than
the trees can. One might speculate that
the microclimate near the ground beneath
the cover of tree stems was less subject
to frost than unshaded shoots at the top of
the crown canopy. In any event, there is
obviously a temporarily productive and
reasonably secure niche at the forest
floor in which the handsome plants can
quickly grow and flower.
In silvicultural practice, we distinguish
between two different kinds of lethal
disturbance. Those intended to replace
old stands with new ones are called re-
generation cuttings; most of the rest of
this talk will be about them. These cut-
tings have to be comparatively large in
areal extent or at least large enough
that new seedlings or small, young trees
rather than old, adjacent ones fill the
vacated growing space.
The other kinds of disturbance, tradi-
tionally called ‘‘intermediate cutting’’,
are those in which scattered individual
trees or, at most, offending vertical strata
of trees, are removed or eliminated to
favor other existing trees. Since cutting is
not always involved, especially with
modern development of tree-killing
chemicals and more purposeful use of
fire, the term ‘‘tending’’ is probably more
appropriate. Anyhow, tending opera-
tions are aimed at guiding or accelerat-
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
Fig. 1.—Typical surface fire burning the grassy forest floor beneath a western
ponderosa pine forest. This common natural phenomenon will kill some of the trees and
pine seedlings will colonize the resulting vacancies. ( U. S. Forest Service photo.)
ing development of established vegeta-
tion rather than its replacement. Such
cuttings, “‘intermediate’’ in time between
the regeneration cuttings, are almost
always in the nature of partial removals.
Stands of forest trees can live so long
and be so infrequently subjected to
disturbance that it is hard to convince
anyone that they are ever disturbed at
all. Many forests owe their present char-
acteristics to rare events which are not
necessarily always destructive. The
forst fire or windstorm of an hour’s
duration once every two or three cen-
turies can govern the vegetational de-
_velopments of the intervening time. In
fact, it is either such events or attacks
by fungal or insect pests which have been
the initiating events of just about all of
our natural forests. Most of the excep-
tions simply involve some less common
kind of lethal disturbance such as land-
slides or volcanic eruptions.
The natural vegetation of any locality is
a kind of repertory of species collectively
adapted to fill virtually any kind of
vacancy or new ecological niche that has
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
come into existence as a result of natural
disturbances (Fig. 2). There are plants
that can claim the minimal growing space
afforded by a rotten knot hole high up
on a tree as well as lichens, algae, and
mosses that colonize the surfaces of
rocks and tree bark. Part of the solution
to silvicultural regeneration problems is
determining the kind of vacancy that
favors the desired species (plural or
singular) more than unwanted competi-
tors.
It is not enough that they be able to get
established; sooner or later, the desirable
trees must be in an environment in
which they can grow faster in height than
the undesirable. Although one can strive
to create the right conditions at the time
new forest vegetation is established,
some sort of corrective action is often
necessary later on.
Some species are adapted to colonize
severely exposed areas, especially those
created by hot forest fires (Fig. 3). These
species, aptly termed pioneers, can en-
dure wide extremes of temperature and
grow fast enough to push their roots
Fig. 2.—Newly germinated conifer seedling;
survival at this stage depends on microclimatic
factors which can be deliberately predetermined
by cutting patterns. (U. S. Forest Service photo.)
quickly below the surface inch or two that
is subject to severe desiccation. They
must grow fast if they are to survive
and require lots of light to support their
rapid growth and high respiration rates.
Among the natural fire-following species
that fall in this category are jack and
lodgepole pines as well as the aspen pop-
lars and certain birches. In silvicultural
practice, the regeneration of such species
usually requires the complete removal of
the old forest in clearcutting; however,
certain other effects of the fires have to be
simulated as well.
In a certain sense, fires kill forests
from the bottom up because the heat is
generated mainly by the burning of the
litter of the forest floor. Some mineral
soil may have to be exposed through
such litter destruction if the seeds of the
pioneers, which are often small and wind-
dispersed, are to have satisfactory con-
tact with the stable moisture supply of
firm soil. It can also be very important
to get the effect of killing of the sub-
ordinate vegetation which often includes
tree species that started under the old
stand but are not necessarily desirable
or well-adapted to the soil conditions.
At the other extreme are the so-called
Sshade-tolerant species that not only
endure shade but also tend to require it
in the early stages of development. These
species have characteristics such as low
respiration rates, high chlorophyll con-
tent, and efficient leaf arrangement that
enable them to stay alive at low light
intensity. Their seedlings do not grow
rapidly in height simply because there
has never been any survival value in
doing so just as they have also sacrificed
much ability to endure exposure.
These species include certain spruces,
most true firs, hemlocks, and most
maples and oaks. They are generally
adapted to persist for many years beneath
old stands of trees but to retain the
capacity for initiating rapid height growth
when released by lethal disturbances that
kill forests from the top downward.
The natural disturbances to which they
are adapted are windstorms (Fig. 4), the
lethal effects of defoliating insects, and
fungi or other pests that weaken tree
stems enough to cause them to break.
Once these so-called ‘“‘advance growth”’
species are established as seedlings or
small saplings, it is possible to release
them in any pattern of space and time
that is appropriate for other management
purposes; however, their regeneration
fails if major removal cuttings take place
Fig. 3.— Very hot crown fire in western conifer
stand. A new natural stand dominated by pioneer
tree species would follow this severe disturbance.
Clearcutting simulates this kind of disturbance
but without certain baneful effects of such highly
dangerous fires. (U. S. Forest Service photo.)
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
ee ee
Fic. 4.—Severe blowdown in a west coast forest. If there is no subsequent
fire (which would be very hot), the new
already present or from progeny of the
Service photo.)
before the seedlings are adequately estab-
lished.
As is usually the case in such matters,
there are lots of species that represent
adaptations to microenvironment that are
intermediate between the extremes just
described. Actually, there is a grada-
tional series of adaptations from one end
to the other. Many of our most important
species fall into this broad intermediate
category. They may individually have
some special ecological requirements
that must be met but they are generally
flexible enough that a variety of regenera-
tion cutting patterns and _ silvicultural
techniques can be applied. Among the
species in this group are Douglas-fir
and such important pines as loblolly,
slash, ponderosa, red, and the five-
needled whites. In nature, most such
species regenerated after fires that killed
many trees but not all of them; however,
it is not wise to generalize much about
this point because windstorms and other
kinds of disturbance were also commonly
involved.
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
forest will develop from advance growth
scattered remaining trees. (U. S. Forest
Much of what I have just said relates
to the applied ecology of securing re-
generation from seeds applied naturally
or artificially out in the forest. While the
silvicultural techniques that closely simu-
late nature often work and have such
advantages as low out-of-pocket cost, it
would be wrong to leave the impression
that they always work or work well when
they do. The numbers of seedlings are
often either too many or too few, some-
times within the same acre. Furthermore,
most trees do not bear seeds every year,
nor does the rain always fall at the nght
time after the seeds fall.
The planting of nursery-grown seed-
lings is a way of by-passing many of
these problems of timing and stand
density. It is also coming to be increas-
ingly prominent as a means of estab-
lishing stands of the progeny of
selected trees.
There are considerations in addition to
the ecological adaptations of young trees
that govern the cutting patterns chosen
to replace forests. All things have to be
7
conducted in the context of economics,
both that of the human needs of the next
century and the frantic concerns of the
present. The society of the day is con-
cerned about its posterity but seldom to
the extent of investing lavishly in it.
A dollar spent on regeneration now is
often required to hold promise of a re-
turn of $46.90 at 8% compound interest
50 years hence. Since society seems to
expect wood to be cheap, harvesting
costs are continually scrutinized and
usually trimmed to the lowest level that
law and prudence will allow.
Logging costs tend to weigh in favor
of clearcutting in large units of area
where the timber is large and on rugged
terrain (Fig. 5). This is because pon-
derous machinery and expensive roads
are required. The costs of roads and of
moving in machinery are fixed costs and
it is desirable to spread them over as
much harvested product as possible.
If the terrain is easy and the trees
smaller, the fixed costs are less signifi-
cant, so more attention is paid to the vari-
able costs. These are basically those of
handling trees one by one and are in-
versely related to tree size. If it costs
more to harvest a unit of produce from
small trees than large, loggers would,
if left to their own devices, cut only the
larger ones.
It would be a remarkable coincidence
if the short-term economic logic involved
in minimizing the costs of one logging
operation also optimized the long-term
net benefit sought in managing a stand of
trees through one rotation from birth to
replacement. Some sort of compromise
must be sought not only between long-
and short-term financial considerations,
but also among all the objectives and
limiting factors involved in forest
management.
One of the key decisions in forest
management and silviculture involves the
question of which parts of a whole forest
should be composed of even-aged stands
and which, if any, of uneven-aged stands.
There are many factors which weigh in
favor of having stands even-aged, or per-
haps more precisely, more nearly even-
aged than otherwise. The reasons why
foresters the world over keep coming
back to policies of even-aged manage-
Fig. 5.—Clearcut patches in Pacific Coast Douglas-fir; the nursery-grown seedlings
that have been planted after the slash burning are too small to be visible. (Photo
by author.)
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
ment are many and variable, although
not of universal validity.
Before proceeding further, it is perhaps
well to point out that even-aged manage-
ment does not require clearcutting. The
technique called shelterwood cutting, in
which a new stand is started under an old
one, is a method of even-aged manage-
ment which becomes prominent when
good forests have been developed (Fig. 6).
Matters of economy in administration,
harvesting, and silvicultural treatment
are certainly factors which favor even-
aged management. It does help and save
money to be able to conduct one kind of
operation at a time over areas some acres
in extent. It becomes both confusing and
costly if one is simultaneously doing all
things appropriate to all stages of stand
age within a patch-work of sub-stands of
differing age.
The alternative policy of uneven-aged
management often requires that the entire
road network of aforest be almost equally
and continuously used. With even-aged
management, operations are more con-
centrated in space, so parts of the road
system can be left out of use for long
periods. This not only saves money but
reduces the amount of erosion-prone
road surface; this is very crucial because
nearly all of the soil and water damage
that can be charged against timber-
production forestry comes from roads.
Another common reason for even-aged
management is simply that most stands
are even-aged already and are difficult to
change. In nature, many stands arise
from the kinds of catastrophic distur-
bance that create even-aged stands. The
very heavy cuttings, with or without ill-
controlled fires, that characterized
logging done without conscious intent of
future management, often left even-aged
Stands. In fact, there are large areas of
the country where the liquidation of old
forests proceeded so rapidly that most of
‘the stands are of nearly the same age;
this creates a situation very difficult for
securing the distribution of age classes
necessary for sustained yield. It is not
possible to change an existing pattern
of age-class distribution in forests with-
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
%
Fig. 6.—Shelterwood cutting in Pacific Coast
Douglas-fir with seedlings about 8 years old that
naturally established themselves in the new en-
vironment created by heavy, partial cutting. (Photo
by author.)
out replacing some trees prematurely or
holding some beyond maturity.
True uneven-aged management, in
which distinctly different age classes
are maintained within a stand, is ap-
propriate to somewhat less common cir-
cumstances. The simplest are where
there are already at least two immature
age classes and it would be wasteful to
liquidate them prematurely. The other is
where there is some reason to want to
have fairly large trees on the ground at
all times. This is logical in certain recrea-
tion or scenic areas and where there is
risk of land-slides. This kind of man-
agement is also useful on small holdings
on which the growing timber is handled
as a kind of fluctuating bank account
with limited silvicultural investment.
Uneven-aged management or the so-
called selection system of silviculture
(Fig. 7) is very difficult to apply if the
goal is to make each small stand a perfect,
self-contained, sustained-yield unit. The
methods for regulating harvests under
9
Fig. 7.—An uneven-aged stand of mixed coni-
fers created by a series of selection cuttings con-
ducted over a 30-year period along a scenic high-
way in a national forest near Crater Lake,
Oregon. (Photo by author.)
such management are both complicated
and highly unreliable. The advocates of
the selection system and of uneven-
aged management often destroy their
case by doctrinaire insistence on making
stands into sustained-yield units. There is
plenty of room for incomplete applica-
tions of the selection system, but it is
better to employ them only where real
reasons exist for doing so and not merely
because of whim or naturalistic mystique.
Nature can create large even-aged
stands and also those with several irregu-
larly distributed age-classes; however,
the theoretical all-aged stand with all age-
classes equally represented would be just
as much of an artificial creation as a
1,000-acre plantation of loblolly pine, and
so much harder to create that none are
known to exist.
In considering some aspects of recent
American silvicultural practice, it is
necessary to point out that it is all still
10
very new as far as the long time-
scale of forestry is concerned. The whole
idea of growing trees consciously really
did not take hold to any significant ex-
tent in this country until the time of
World War II. Most forestry on industrial
holdings started about then. Before that
time, most public forests were regarded
as economically inaccessible so they
were protected, but little was harvested
from them.
Part of the reason why there is so
much clearcutting now is that foresters
of today have inherited a large backlog
of stands in need of replacement. Some
of these are the rather degraded kinds of
vegetation left over from decades or from
centuries of reckless cutting and inade-
quate protection. Others may be tottery
old-growth stands that do not stand up
well under partial cutting and consist
largely of over-mature trees. Stands of
this kind must generally either be re-
served as museum pieces or replaced by
clearcutting. It is very probable that there
are lots of sites on which clearcutting
will be a one-time-only operation as a
stage-setting device and that subsequent
stands will be handled by some variant
of the shelterwood method. This method
provides plenty of ways of getting the ad-
vantages of partial cutting under even-
aged management, but it is hard to apply
unless one has already created a good,
vigorous and accessible forest.
Clearcutting is also involved in the
quasi-agricultural kinds of silviculture
aimed at intensive timber production.
If thorough-going treatments with
machinery or fire precede planting and if
no reliance is placed on natural seeding,
then it is expedient to employ clear-
cutting and planting. At present, one of
the chief reasons for doing this is the
attempt to establish genetically superior
forests. This approach is_ especially
fashionable on industrial holdings. Pre-
vious experience makes it logical to
anticipate that it will work well with
some species and on some soils, but that
it will fall victim to insects, fungi,
wind and other damaging agencies else-
where. In some instances, the high ex-
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
pense will prove richly rewarding but in
others there will be disappointment. The
important thing is that this technique
cannot be embraced as a universal solu-
tion nor condemned out of hand as a
violation of nature; however, it does
work best on somewhat dry sites where
fire has been common in nature and has
also produced rather simple stands of
fast-growing pioneers.
There is no one best way of treating
all forests; they are simply too variable
in their natural behavior and in the socio-
economic circumstances that affect their
management. The forests of this country
are not only vast in extent but they in-
clude just about every kind of forest
that might be found outside the tropics
and even some of those. Furthermore,
the silviculture that was best for the forest
of a paper company on one side of a
fence would differ from that of a bank
teller on the other side.
The best decisions about silviculture
practice are made by experienced, ob-
servant foresters on the ground who have
the capacity, responsibility and authority
for the necessary analytical thought. At-
tempts to dictate silvicultural decisions
from distant points are inevitably based
on sweeping, simplistic generalizations.
Even if the prescriptions from distant
sources fit 80% of the cases well, some
disastrous failures can result from the
20% that do not fit. It matters not
whether the distant source of authority
is a legislature, the headquarters of either
a government bureau or a corporation, or
some university ivory-tower.
It has recently become fashionable to
decry the techniques of silvicultural
practice as a kind of ecological desecra-
tion. This is almost as far from the truth
as one can get. Even the most artificial
kind of forest must be quite close to
a state of nature; if it isn’t, it does not
endure anyhow. It is logical to be con-
cerned about the erosion which roads
and other soil disturbance can induce.
Much of this can be prevented. Never-
theless, it is perhaps often overlooked
that the worst forestry causes far less
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
erosion than the best of clean-cultivation
agriculture. All living resources are re-
newable and there appear to be none
more infinitely renewable than those of
the forest. Furthermore, of all of the
structural substances used by our civi-
lization, there is none which can be
produced and used with less input of
energy than wood. Provided that efforts
to clean up pollution from wood-pulp
mills continue, it can also be said that
none give less output of pollutants.
This country has a lion’s share of the
world’s productive forest land. It is no
recommendation for our past per-
formance that we are net importers of
timber and will probably remain so into
the next century even if we start even
greater intensification of forestry now.
The question of whether we can put
American forestry into the same key role
as American agriculture depends on what
is done in managing the myriad of small
ownerships. These include not only the
majority of the forest area but also a
very high proportion of the most produc-
tive and accessible land. The contribu-
tion from public and industrial forests
can certainly help, especially in the near
term, but it cannot be enough to carry
all the burden. ©
Our best hope for indefinite economic
survival may lie in nuclear power; our
surest hope is in protecting and using the
productive capacity of our field and forest
soil.
Bibliography
Hermann, R. K., and D. P. Lavender (Ed.) 1973.
Even-age management, proceedings of a sym-
posium held August 1, 1972. Oregon State
University, School of Forestry Paper 848. 250 p.
President’s Advisory Panel on Timber and the
Environment. 1973. Report. U. S. Government
Printing Office, Washington. 541 p.
Smith, D. M. 1962. The practice of silvicul-
ture. 7th ed. Wiley, New York. 578 p.
Spurr, S. H., and B. V. Barnes. 1973. Forest
ecology. 2nd ed. Ronald, New York. 571 p.
U. S. Forest Service. 1973. Silvicultural systems
for the major forest types of the United States.
U. S. D. A., Agric. Hbk. 445. 114 p.
11
Washington Junior Academy of Sciences
Christmas Convention, 1976
Elaine G. Shafrin, e¢ al.
Washington Academy of Sciences Committee on Encouragement of Science Talent
Each year the WJAS sponsors a Christ-
mas Convention at which high school
students have the opportunity to present
their research in a format similar to that
of professional society meetings. A call
for papers is issued to all public, pri-
vate, and parochial high schools in the
Greater Washington Metropolitan Area;
participation is not limited to WJAS
members. From the written theses re-
ceived in response, a panel of adult
scientists and educators selects a limited
number for oral presentation by the
student author in an auditorium before
the Convention audience of WJAS mem-
bers and interested adults. Provisions
are made for a question period fol-
lowing each presentation. A second
panel of judges then evaluates the
presentations. Modest monetary awards
(from $5.00 to $20.00) are presented for
the highest ranked papers. Additionally,
the student winning the first prize is
sent to represent the WJAS at the Na-
tional Meeting of the Association of
Academies of Sciences, held in con-
junction with the AAAS Meeting.
The 1976 Convention was held on
Saturday, Dec. 18, at the NASA-God-
dard Space Flight Center. The program
was organized and chaired by Gary
Neben, WJAS Vice-President and a
senior at Herndon High School. The
morning session was devoted to the
student presentation of the eight papers
for which the abstracts appear below.
The papers were judged by a panel
recruited by Dr. Russell W. Mebs, a
Senior Advisor to the WJAS. In addi-
tion to Dr. Mebs (physicist, retired
from NBS), the panel comprised Mr.
Alfred Gunnersen, Jr. (mathematician,
TRW), Dr. Peter H. Heinze (plant
12
physiologist and biochemist, retired from
USDA Agriculture Research Center),
Dr. Jay Lee Mead (astronomer, NASA),
and Mr. Joseph Pearlstein (technical
writer, retired from the Harry Diamond
Laboratories). Following a brown-bag
lunch there was a tour of the NASA
facility, conducted by Mr. Elva Bailey of
the NASA staff. Highlights of the tour
were the visit to the Master Control
Room and Communications Center. The
Convention then reconvened for the pre-
sentation of Certificates of Commenda-
tion to the student authors, the judges,
and Mr. Bailey. After presentation of
cash prizes to the authors of the four
papers ranked highest by the judges for
this year’s Convention, the announce-
ment was made that the winner of the
1975 Convention, Miss Allison Stark,
would be attending the AAAS Meeting
in Denver, Colorado in February, 1977.
Appreciation was then expressed to Mrs.
Dayna Smith, Senior Advisor to the
WJAS, for her efforts in coordinating
the meeting and to the ,TRW Company
which had donated the money which
made possible the granting of financial
awards.
Abstracts of the papers are presented
here. The first four projects won first,
second, third, and fourth places in the
order in which they appear.
THEOREM OF THE CARDINALITY OF
INFINITE PERMUTATION SETS
Dwight Barkley
Crossland High School, Camp Springs, Md.
The theorem presented in this paper
states that the cardinality of an infinite
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
ordered set, S, is transcended by the
cardinality of the permutation set (the
set of all possible permutations) of S. The
proof makes use of the indirect method
by assuming that there exists a one-to-
one correspondence between S and the
permutation set of S. This is then re-
duced to a contradiction by finding a per-
mutation of the elements in the set S that
could not be in the range of any one-to-
one mapping of S onto the permutation
set of S. The proof of the theorem
then follows immediately from the fact
that S is a subset of the permutation
set of S.
Throughout the proof of the theorem
no inferences have been made as to the
kind of infinite ordered sets involved.
This permits this theorem to be appli-
cable to any kind of infinite ordered
set, numerical or abstract, and so other
infinite sets may be constructed from
pre-existing sets. Also, this theorem
provides a direct way of comparing
the cardinality of certain known sets.
Thus the theorem developed in this
paper provides the field of mathematics
with another theorem, which adds to its
ever growing structure.
ENZYME KINETICS— POSITIONAL EFFECT
OF AN ORGANIC GROUP ON INHIBITIONS
Lawrence R. Weatherford
West Springfield High School, Springfield, Va.
Indole is known to be a competitive
inhibitor of alpha-chymotrypsin. A proj-
ect was undertaken on the hypothesis
that each time methyl groups were
attached to various positions on indole,
a unique effect on inhibition of the
enzyme would result. Kinetic rate con-
stants were determined for 4 different
methyl analogs. Using this data, an ex-
planation of the observed effect in terms
of a bonding analysis was determined.
Project results revealed that there are
varied effects among the methyl analogs
and that there are 3 prominent factors
which determine the unique effect which
the inhibitor has upon the enzyme.
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
THE DIFFERENTIAL EFFECT OF SILVER
NITRATE SOLUTIONS ON Herpes simplex
VIRUS
Kenneth Johnson
Sidwell Friends School, Washington, D. C.
The antiviral capabilities of varying
silver nitrate (AgNO,) solutions was
tested on Herpes simplex virus types 1
and 2 in Vero cell cultures, using a plaque
neutralization assay.
The stock virus suspensions were di-
luted to contain the desired number of
plaque forming units. The virus titrations
and dilutions of silver nitrate were car-
ried out, using 10-fold dilutions. The 2
diluents used for silver nitrate were
lactalbumin hydrolysate (LAH) and
12.5% ethyl alcohol. Equal volumes of
silver nitrate and the diluted test virus
were combined. LAH and ethyl alcohol
controls were used as a test for tissue
toxicity.
Falcon flasks containing Vero cells
were inoculated with the test virus dilu-
tions. The flasks were incubated for 1 hr
at 37C. After the incubation period,
nutrient agar overlay was applied to the
cell cultures. The flasks were then in-
cubated for 5° days’ at 37 €. The test
was stained on day 5 using a similar
agar overlay containing neutral red. The
flasks were incubated for 24 hr at 37 C;
after the incubation period, all viral
plaques were recorded.
The experiment verifies the fact that
silver nitrate solutions effectively in-
activate both strains of Herpes viruses.
Silver nitrate solutions exhibit greater
effectiveness against type 1 HSV than
against type 2 HSV. Herpes type | shows
greater sensitivity to both forms of
silver nitrate solutions. Type 2 viral
activity is greatly reduced in solutions
of silver nitrate containing ethyl alcohol.
It is believed that ethyl alcohol aids
in virus inactivation by eliminating the
lipoprotein envelope surrounding the
virion. The antiviral effects of silver
nitrate may be due to the concentra-
tions of silver ions held in the final
13
solution. It is possible that the silver ions
may bond to the lipoprotein envelope,
altering the viral receptor sites. Since the
virus can no longer attach itself ef-
fectively to the cell surface, it loses its
potential for infectivity.
This experiment might prove useful as
a simple, effective laboratory method to
differentiate between Herpes type 1 and
type 2 strains due to the 2 different
rates of viral inactivation.
ANALYSIS OF DATA DESCRIBING GAMMA
RADIATION PRODUCTION FROM
POSITRONEUM DECAY IN
VARIOUS SOLIDS
Bruce Reynolds
West Springfield High School, Springfield, Va.
When high-energy positrons interact
with a metal or crystal, a stable atom
called positroneum is formed. This atom
consists of a positron and an electron
circling each other. Eventually, the two
particles will circle into each other
(attracted by opposite charge), and an-
nihilate. The 2 gamma rays that are
created will be expelled at an angle of
about 180°. The extra momentum car-
ried by each particle in the positroneum,
however, will be transferred to the
gamma radiation, where it will manifest
itself in the shrinking of the 180 degree
angle to 179 or 178 degrees. By measuring
this angle we can calculate the mo-
mentum distribution of the electrons in
the positroneum. Because these elec-
trons are selected randomly from the
free electrons in the target, they are
completely representative of these free
electrons.
Analysis of this data is useful in a
number of different areas: first, Fermi
levels, knowledge of which is in de-
mand now for studies of magnetism of
alloys, can be calculated. Second, the
free electron theory of metal can be
verified. Third, positroneum can be used
to study electron vacancies in semi-
conductors and crystal imperfections.
14
THE EFFECTS OF PHOSPHATE DETERGENTS
ON THE RESPIRATORY AND EXCRETORY
RATES OF Carcinus maenas
John Ross
Sidwell Friends School, Washington, D. C.
The effects of different concentrations
of phosphates on the respiratory and
excretory rates of the green crab,
Carcinus maenas , were analyzed at mean
summer temperatures. Household deter-
gent was used because of its prevalence
and its importance as a major form of
phosphate pollution found today.
Results support the theory that phos-
phate detergents at high concentrations
produce a greater strain on the me-
tabolism of C. maenas than pure phos-
phates at the same concentration. At
low concentrations pure phosphates have
a greater effect on C. maenas’s metab-
olism than the low concentration, low
phosphate detergent.
WHAT ARE THE EFFECTS OF THE OCEAN
ON THE TOPOGRAPHY OF AN ESTUARINE
ENVIRONMENT— THE MAIDFORD RIVER
Gary Smith
McKinley High School, Washington, D. C.
In the past several years the Maid-
ford River has been of great interest
to SPSO students. My problem was to
study the effects the ocean had on the
topography of the Maidford. Profiling
was the technique used to study the
topography. By contouring the results,
the mouth of the Maidford appeared to
fluctuate, while the river itself seemed
to remain unchanged.
METALLURGY: THE GROWING OF THE
CRYSTAL
Mary Drennan
West Springfield High School, Springfield, Va.
Metallurgy is the art and science
which is concerned with metals and their
alloys. It deals mainly with the recovery
of the metal from its ore, its refining,
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
alloying with other metals, forming, fab-
ricating and testing, and a study of the
relation of alloy constitution and struc-
ture to mechanical properties.
The major aspect dealt with here is
the formation of metal crystals through 1
of 3 methods. Although the Czochralski
and horizontal methods are discussed,
it is the Bridgman technique that is
of the greatest importance because of its
simplicity. The metal lead was used be-
cause of its low melting point.
Even though seeds of lead crystals
were formed, it can clearly be seen that
the technique used in this paper needs
to be refined. Some of these adjustments
are that the metal needs to be melted
and the crucible should be a sealed
one. A clear crucible would be helpful.
Being able to recrystallize metal is a
basis for the hot and cold workings in
industry. When the technique is carried
out correctly it is a useful tool for
mankind and industry.
MODULATION OF HUMAN LECTIN-INDUCED
LYMPHOCYTOTOXICITY
Alexander Zaras
Washington-Lee High School, Arlington, Va.
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
The effects of EDTA, cold, colchicine,
cytochalasin B, and trypsin were studied
on an autologous lectin-induced lympho-
cytotoxicity system. The various agents
were added to an in vitro system con-
taining °!Cr-labeled target red blood cells,
effector peripheral human blood lympho-
cytes, and a lectin. The degree of
cytotoxicity was determined by the
amount of °'Cr release.
We found that cold, by lowering the
metabolic activity of the cell, inhibited
cytotoxicity. EDTA inhibited cytotox-
icity due to disruption of cell-to-cell
contact. Both colchicine, which disrupts
microtubules, and cytochalasin B, which
disrupts microfilaments, were observed
to inhibit cytotoxicity. The addition of
trypsin resulted in increased cytotox-
icity, presumably due to the uncovering
of new receptor sites on the cell
surface.
These experiments indicate that neces-
sary requirements for autologous lectin-
induced lymphocytotoxicity include a
metabolically active cell, cell-to-cell
contact, intact microtubular and micro-
filament systems, and adequate numbers
of appropriate surface receptors for the
inducing agent.
15
REVIEW
Chemical Communication in Insects!
May Inscoe
Organic Chemical Synthesis Laboratory, Agricultural Environmental
Quality Institute, Beltsville Agricultural Research Center, ARS,
USDA, Beltsville, Maryland 20705
ABSTRACT
Many aspects of insect behavior are regulated by minute amounts of chemicals
with highly specific action. Insects may use such compounds in finding mates, locat-
ing food or suitable sites of oviposition, recruiting workers, warning others of attack,
and driving off enemies. As research on the nature and mode of action of these
materials progresses, applications in insect pest management programs will increase.
Insects are greatly dependent on
chemical signals throughout their lives.
They find food and mates and suitable
locations for oviposition by following
chemical cues from other insects and
from their surroundings. We can think of
numerous examples. For instance, a
column of ants carrying crumbs from a
picnic table back to the ant hill is guided
by the chemical trail laid down by the for-
aging ants that first discovered the food
supply. When a swarm of honey bees,
Apis mellifera L., is ready to move to a
new nesting location, scouts are sent out
first. When they return, the swarm sub-
sequently follows these scouts to the new
site, depending for guidance on chemicals
the scouts give off. Unless the swarm
senses the presence of the queen through
her scent, however, many of the bees
turn back (Morse, 1963). The presence of
"A talk presented at the 559th meeting of the
Washington Academy of Sciences on February 19,
1976;
16
a worker bee which has been treated with
a queen bee extract fools the swarm
enough that most of the bees will fly to the
new site without a queen (Avitabile et al.,
1975); several different chemicals may be
involved in this swarming behavior.
Mosquitoes use chemical cues to find
humans to bite and suitable waters for
egg-laying. Perhaps the most dramatic
examples of chemical communication are
found in the various steps in insect mat-
ing. In this area the chemicals can be ex-
tremely effective in minute amounts. It
has been reported that a single female
introduced pine sawfly, Diprion similis
(Hartig), in the five days of her adult life,
was responsible for attracting the 11,000
males that were caught on the sticky
board surrounding her cage (Coppel et
al., 1960).
It may be argued that such uses of
chemical cues do not constitute com-
munication in the strictest sense. Never-
theless, for want of a better term,
‘‘chemical communication’ has become
fairly standard usage. In a developing
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
field of interest such as this, many terms
are coined to convey specific meanings
and those that are found useful by others
eventually gain acceptance. ‘‘Semio-
chemical’’ is such a term, meaning a
chemical that carries a message (Law
and Regnier, 1971). Originally this term
referred only to naturally-occurring sub-
stances, but chemicals from other
sources are now often included.
Natural semiochemicals may be phero-
mones, allomones, or kairomones, three
other recently-coined words. A phero-
mone (Karlson and Liischer, 1959) is a
substance secreted or emitted by one
member of species that brings about a re-
sponse in another member of the same
species. The attractant emitted by that
female sawfly I mentioned is a sex
pheromone. Pheromones are intraspe-
cific semiochemicals, acting within a
species, affecting members of the same
species. Allomones and kairomones, on
the other hand, are transspecific (or inter-
specific); the emitter and the receiver be-
long to different species; transspecific
semiochemicals have been called allelo-
chemics (Whittaker, 1970; Whittaker and
Feeny, 1971). An allomone is ‘‘a chemi-
cal substance, produced or acquired by
an organism, which, when it contacts an
individual of another species in the
natural context, evokes in the receiver a
behavioral or physiological reaction
adaptively favorable to the emitter’
(Brown, 1969). The reaction produced by
a kairomone benefits the recipient of the
message rather than the emitter (Brown
et al., 1970). Thus, the scent of a skunk
would be considered an allomone, since
it repels the skunk’s enemies, while the
rabbit odor that enables a fox to locate
its prey is a kairomone, since the re-
ceiver (the fox) is benefitted by the mes-
sage. These terms are not mutually ex-
clusive. A bark beetle sex pheromone,
frontalin, is used by some bark beetle
predators to-locate their prey (Vité and
Williamson, 1970); thus, it is both a
pheromone and a kairomone.
Insect hormones, which act internally
within a single insect, do not fit into the
scope of this discussion.
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
Examples of Non-Chemical Communication
I do not want to give the impression
that all insect communication involves
semiochemicals, for this is far from being
the case. Chemicals are probably the
most widely used means of insect com-
munication, but many other methods are
also known. Firefly lights, for example,
can be mating signals. The males fly
about, flashing in a pattern characteristic
for their species, and females on the
ground or on low perches flash answers
back. A male receiving a correct answer
to his flashed message, with the appropri-
ate flash length and delay, comes closer
and repeats his pattern. This dialogue
continues until the male reaches the fe-
male. There is not always a happy ending,
however, for some predatory females
seem to have broken the code used by
other species and have been observed
to attract males of other species by
mimicking the appropriate female re-
sponse and then to devour the male when
he gets within range (Lloyd, 1975).
Both a rat mite, Laelaps echidnina
Berlese, (Bruce, 1974) and a bark beetle
parasite (Richerson and Borden, 1972)
have been reported to find their hosts by
sensing the emitted infrared radiation.
Some planthoppers find their mates by
means of vibrations. Females on a rice
stem vibrate their abdomens, and males
elsewhere on the plant sense the vibra-
tions and respond if the frequency is right
(Ichikawa et al., 1975).
Some male cicadas attract females by
their stridulation, or singing. This can be
unfortunate for them, for one parasitic
fly locates cicadas by means of this song,
with the result that males are more fre-
quently parasitized than females (Soper
et al., 1976).
Perhaps the best known non-chemical
means of communication is the honey bee
waggle dance which foraging workers
use to inform other workers of the loca-
tion of a food source. The straight-line
portion of the dance pattern indicates the
direction, while the waggle frequency
shows the distance (von Frisch, 1946,
1974). Odors are also involved in relaying
this information (Gould, 1975).
17
Many other examples of non-chemical
means of communication could be cited,
but that would be beyond the scope of this
paper. My purpose is to outline some of
the many roles semiochemicals play in
the lives of insects and in their interac-
tions with other insects and with their
environment. More detailed information
can be obtained from some of the
numerous comprehensive reviews on
various aspects of the subject, as, for
example, Birch, 1974a; Eisner, 1970;
Jacobson, 1972. Although a goodly num-
ber of these chemicals have been identi-
fied, many others are recognized only
through their action. Our information in
this area is far from complete.
Insect Olfaction
To receive the messages carried by
these chemicals, insects must have some
means of detecting them. Although a few
pheromones seem to be detected by tast-
ing, in most cases the detectors, or
chemoreceptors, are found on the an-
tennae (Schneider, 1974). Since it ap-
pears that the process of chemorecep-
tion by insect antennae is comparable to
that whereby odors are detected by the
human nose, the process is often referred
to as insect olfaction (Schneider, 1969).
Hopefully, studies of insect responses to
semiochemicals will lead to increased
understanding of how we detect and dis-
criminate between various odors. Con-
versely, progress in mammalian olfaction
and gustation may contribute to the
understanding of insect chemoreception.
Studies of insect olfaction rely greatly
on the electroantennogram (EAG)
(Schneider, 1957), which is a measure-
ment of the electrical response of an
antenna to a chemical stimulus. EAGs
have great utility in studies on the nature
and mechanism of action of pheromones
and in the identification of pheromonal
components (Arn et al., 1975).
Insects also have chemoreceptors
that correspond to our taste buds, but
gustation and general food attractants are
not considered here.
18
Sex Pheromones
Up to now, insect sex pheromones are
the insect semiochemicals that have re-
ceived the most intensive study. Natural-
ists have believed for a long time that
scents were responsible for mate-finding
by various moths. As long ago as 1690,
for example, John Ray, a biologist, noted
several male moths, Biston betularia (L.),
fluttering around a cage in which a fe-
male of the species had just emerged
from her chrysallis; in reporting this, he
suggested that the scent of the female
had attracted the males from outside
(Mickel, 1973). Early collectors added
rare specimens to their collections by
using caged females as lures. The French
naturalist Fabre (1900) published ob-
servations on various male moths at-
tracted through open windows by caged
female moths; one species of moth re-
sponding in this way had not been found
in the area in twenty years.
By the early 1900’s, then, it was well
known that attractive materials given off
by female moths of many species attract
males and that these materials are very
specific in their action. In moths, this
material is usually produced by glands in
the female abdominal tip, and females
emitting the attractant lift the tips in a
characteristic position referred to as
‘‘calling’’. The gypsy moth, Lymantria
dispar (L.), is one insect that has received
intensive study. Even in 1914, traps
baited with live female gypsy moths
were being used to locate new infesta-
tions of this forest defoliator and to
delineate the extent of existing infesta-
tions (Collins and Potts, 1932). However,
all females are not equally attractive,
they live only a few days, and they are
available for only a short time, so there
are many factors limiting the utility of live
female gypsy moth traps. In addition,
there is always the possibility that a live
female could escape and start a new in-
festation. By 1920 it had been found that
extracts of female abdominal tips could
be used in place of the live females,
thus overcoming many of these ob-
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
ee SSeS
stacles. The discovery in 1944 (Haller et
al., 1944) that hydrogenation of the ex-
tract increased its stability and attractive-
ness was another forward step. Never-
theless, without a knowledge of the
chemical composition of the attractant,
entomologists were dependent upon live
insects to obtain the lure extracts for
gypsy moth survey traps. The supply of
these insects in the USA is very erratic;
for several years, moths were collected
in Spain to prepare extracts for USDA
survey traps.
Widespread attempts at identifying the
attractant pheromones of different in-
sects continued, but it was not until 1959
that the identification of a sex phero-
mone, that of the silkworm moth, Bom-
byx mori (L.), was reported (Butenandt
et al., 1959). This accomplishment had
required 20 years of careful experimenta-
tion, and half-a-million female phero-
mone glands were used. By an involved
series of separation steps about 6 mg of
pure substance was isolated from the
extract of these glands. Microchemical
studies (hydrogenation and permanga-
nate oxidation) and synthesis showed
this pheromone to be (£,Z)-10,12-hex-
adecadien-1-ol, called bombykol.
One requirement in pheromone iden-
tification studies is an adequate sup-
ply of insects, both as a source of phero-
mone and also as test subjects for use in
following the isolation and purification
steps. Butenandt and his group had in-
sects readily available—silkworms have
been ‘‘domesticated’’ for 4000 years at
least. With other insects this has been a
severe limitation. Unless a successful
method for rearing has been developed,
wild insects must be used and these
may be available only for a limited time—
sometimes not more than a week or two
each year. Rearing insects is no easy
task. Problems with diet and disease
are but two of the many difficulties en-
countered. _
Another requirement for successful
pheromone identification is a good
method of bioassay. Insects, like all liv-
ing things, are extremely complex mix-
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
tures of chemicals, and to sort out the
minute amount of unknown material from
the relatively massive amounts of other
similar and dissimilar chemicals, it is
necessary to have some means of moni-
toring each step in a separation to lo-
cate the fraction containing the active
material. The product of the pheromone
gland of the female silkworm moth at-
tracts males and causes intense excita-
tion, with wing vibration and a circling
sort of dance. Butenandt used the wing
vibration in his bioassay, and his ‘‘unit
of attraction’’ was defined on the basis of
the concentration of material that would
cause at least 50% of the males in a cage
to start this vibration when a glass rod
dipped into the solution was introduced.
We now know that the attractive com-
_ponent (or components) in the phero-
monal emission of a female moth is not
necessarily the same as that causing
stimulation, and the search for attractant
pheromones cannot depend exclusively
on a stimulatory response as a method of
bioassay. The ultimate test of an at-
tractant is a field test, and thus far there
have been no reports of field tests with
bombykol. After all, the silkworm is not
a pest insect, so bombykol has not
been needed for survey trapping, which is
the means by which other pheromones
have received the most extensive testing.
It seems probable that bombykol is in-
deed an attractant as well as a stimulant,
but this point needs clarification.
In the sixteen years since the discovery
of bombykol was announced, many other
attractant pheromones have been identi-
fied. This has been accomplished largely
through advances in analytical methodol-
ogy, such as microchemical techniques
and instrumentation for chromatographic
separations and spectrophotometric
measurements. By now, more than 70
compounds have been identified as at-
tractant pheromones, and several other
compounds that are attractive seem to be
pheromones but have not been rigorously
proven to be present in the insect (Inscoe
and Beroza, 1976).
Since the response of male moths to
19
‘‘calling’’ females is generally very spe-
cific, it had been thought that attractant
pheromones would be species— specific.
This is not necessarily so. (Z)-11-Tetra-
decen-1-ol acetate, for example, has been
identified in the attractant pheromone of
10 different moth species and is attractive
in the field to males of 12 other species,
making 22 species in all thus far. In 13
of these 22 species, another compound
is also needed for maximum attractancy.
This requirement of more than one
compound for attraction is rather typical
of the complexities we are encountering
as we learn more about the sex phero-
mones (Silverstein and Young, 1976).
Very often, precise ratios of two or more
components are found to be needed.
With many moths that require two
pheromonal components, the compounds
are closely related chemically. For ex-
ample, they may be opposite geometric
isomers, differing only in the arrange-
ment of atoms around a double bond
(Berozaet al., 1973a); positional isomers,
having double bonds in different posi-
tions on the carbon chain (Meijer et al.,
1972; Tamaki et al., 1971); homologues
(Nesbitt et al., 1975); or compounds with
different functional groups, such as an al-
cohol and the corresponding acetate
(Roelofs et al., 1975), or an aldehyde
and an acetate (Kochansky et al., 1975Sb).
The European corn borer, Ostrinia
nubilalis (Hiibner), provides an interest-
ing example. This insect was introduced
into North America from Europe in
broom corn shipments two or three dif-
ferent times between 1909 and 1914 and
was first established in areas where
brooms were manufactured. It spread
fairly rapidly, though, and now it is a
pest in most of the major corn-producing
regions east of the Rocky Mountains.
In the early 1970’s scientists in Iowa
reported that male moths responded to
(Z)-11-tetradecen-l-ol acetate found in
the female pheromonal emission and
that the opposite isomer, (£)-11-tetrade-
cen-l-ol acetate, inhibits this response;
so that in the presence of more than 15%
E isomer, no moths are attracted by the
Z isomer (Klun and Robinson, 1971).
20
Despite this inhibition, it was soon
found that small amounts (about 3%) of
the E isomer are needed for attraction
(Klun et al., 1973). In New York, on
the other hand, it was found that it is
the E isomer that is attractive to the
males and is the major component of
the female pheromone (Roelofs and
Comeau, 1971; Kochansky et al., 197Sa).
Cooperative trapping studies (Klun and
Cooperators, 1975) have recently shown
that in most of Europe (Austria, Ger-
many, Roumania, Poland, France,
Spain, and Switzerland) and of North
America (lowa, Missouri, Minnesota,
Nebraska, Georgia, Wisconsin, and
several Canadian provinces), males re-
spond to the Z isomer containing small
amounts of the E, while in Italy, Nether-
lands, and New York, males prefer the
other blend—E with a little Z. In Penn-
sylvania and New Jersey both kinds of
response are found. This seems to indi-
cate that the New York strain was
brought to North America in a shipment
from Italy and for some reason has not
spread very far, while the major strain
in North America came from elsewhere
in Europe. Where the habitats of the two
strains overlap, there seems to be practi-
cally no hybridization.
In addition to the attractant phero-
mones, other compounds may have a
marked effect on the number of insects
caught in attractant traps. I have al-
ready mentioned the inhibitory effect of
large amounts of the minor isomer of
the European corn borer pheromone.
Other compounds drastically reduce trap
catches of other insects, sometimes com-
pletely eliminating the attractancy even
when present only in trace amounts.
Compounds of this type have been called
inhibitors or masking agents. Other
compounds have been found that do not
appear to be attractive in themselves
but increase the effectiveness of a lure;
these have been referred to as synergists.
Compounds of both types have been
found in pheromonal emissions.
Now we are finding that the terminol-
ogy we have been using may be mis-
leading (Kennedy, 1972). It is possible
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
that some of the compounds we consider
attractant pheromones because they en-
able males coming from a distance to lo-
cate the females may not be attractants
at all but may be acting as stimulants,
activating the males to fly up-wind and
search for the females; those that blunder
into the traps in the course of their
searching get caught. Other compounds
seem to be true attractants, causing
direct orientation to the source of emis-
sion. We are also finding that some of the
so-called synergists do not act merely to
increase the effectiveness of an attractant
but play a definite role in the response
of male moths, such as increasing the
frequency of alighting (and thus increas-
ing the probability of being caught in a
trap) (Cardé et al., 1975). Similarly, a
compound that reduces trap catches
when it is exposed in a trap with a lure
and is therefore classed as an inhibitor
may actually increase trap catches when
disseminated over the surrounding area
(Mitchell et al., 1974; Rothschild, 1974).
It is obvious that we know very little
of how the sex pheromones work, and
more behavioral studies are needed to
clarify the function of various pheromone
components and the point in the mating
sequence at which each acts.
In most moth species that have been
studied, the female attracts the male for
mating. In fact, in some species the
females have no wings (Tvermyr, 1969)
and must rely completely on their at-
tractant pheromone to bring males to
them. Attractant pheromones may act
over long distances. In one instance, a
marked male moth was recaptured in a
trap, baited with synthetic pheromone,
7.5 km from where he had been re-
leased the previous day (Kochansky et
al., 1975b). Lepidopteran attractants that
have been identified thus far have been
long-chain (10-18 carbon atoms) com-
pounds of relatively simple structure,
usually with one or two double bonds.
Acetates are the compounds reported
most frequently; numerous alcohols and
aldehydes are also active. A ketone, (Z)-
6-heneicosen-11-one (Smith et al., 1975),
a hydrocarbon, 2-methylheptadecane
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
(Roelofs and Cardé, 1971), and an epox-
ide, cis-7,8-epoxy-2-methyloctadecane
(the gypsy moth pheromone, called dis-
parlure) (Bierl et al., 1970), have also
been identified as lepidopteran phero-
mones. In insect orders other than the
Lepidoptera, the situation seems more
complex. Attractant pheromones are
produced sometimes by the male, some-
times by the female, and a wide variety
of structures have been found.
In the boll weevil, Anthonomus
grandis Boheman (a coleopteran), for
example, the male produces a pheromone
that is attractive to females but that also
attracts other males early and late in the
season. It may therefore also be regarded
aS an aggregation pheromone, bringing
insects of both sexes together. Four
components, all having cyclic structures,
have been identified, and some combina-
tion of at least three of these is necessary
for attraction (Tumlinson et al., 1969).
Bark beetles, which are very destruc-
tive in evergreen forests, also emit ag-
gregating pheromones (Borden, 1974).
In various species of Dendroctonus, in
which the male is monogamous, a female
finding a suitable tree starts boring a mat-
ing chamber and emits a pheromone,
which, in combination with volatile ma-
terials from the tree, is very attractive
to males, as well as being an aggregating
pheromone (Renwick and Vité, 1969;
Wood, 1970). InJps spp. the polygamous
male is the one that starts boring into the
tree and gives off a pheromone advertis-
ing for mates as well as attracting other
males to attack the tree (Wood, 1970).
This is a great oversimplification, for
bark beetles of both sexes emit a variety
of pheromones.
The sex pheromones I have mentioned
thus far have served to bring insects to-
gether for mating. Other sex pheromones
may act to make the female more recep-
tive. Some male butterflies have complex
glands (‘‘brushes”’ or ‘‘hairpencils’’) that
are the source of aphrodisiac phero-
mones that release mating behavior in the
female (Birch, 1974b). Male queen but-
terflies, Danaus gilippus berenice
(Cramer), brush “‘hairpencil dust’’ onto
21
flying females to induce them to alight
(Pliske and Eisner, 1969). Certain male
cockroaches give off ‘‘seducin,”’ a vola-
tile substance that has not been identi-
fied, which induces the female to feed
on a liquid oozing from the male tergal
glands and makes her receptive to mating
(Roth and Dateo, 1966).
Trail Pheromones
Pheromones other than sex phero-
mones are also known and are particu-
larly important in the lives of social
insects. Among these are the trail phero-
mones, which are used by ant or termite
foragers returning to the nest with food.
Ants heading home extrude their sting
and deposit streaks of chemical on the
path. Other workers following the trail
reinforce it as long as food is found, but
workers returning empty-handed no
longer deposit the pheromone and the
trail soon fades away. Ants will follow
an artificial trail drawn with contents
of the pheromone gland from a single
ant and mill around in confusion at the
end of the trail (Wilson, 1963). Up to
now, very few trail pheromones have
been isolated and identified, although
many insects have been shown to use
such pheromones. Of the ten compounds
that have been reported, six are used by
one ant species; these are fatty acids
with 6 to 12 carbon atoms (Huwyler
et al., 1973). The other four known trail
compounds are an alcohol, (Z,Z,E)-
3,6,8-dodecatrien-1-ol (Matsumara et al.,
1968), an ester, methyl 4-methylpyrrole-
2-carboxylate (attalure) (Tumlinson ef
al., 1972), a macrocyclic hydrocarbon,
12-isopropenyl-1,5,9-trimethyl-1,5,9-
cyclotetradecatriene (Birch et al., 1972),
and a heterocyclic compound, 3-butyl-
octahydro-5-methylindolizine (Ritter et
al., 1973). All together, four ant and
eight termite species have been found to
use one or another of these ten compounds.
Alarm Pheromones
These trail pheromones recruit work-
ers for food-gathering. Other phero-
mones may recruit for defense; some of
22
the alarm pheromones have this function
(Wilson, 1975b). Alarm pheromones
(alerting pheromones) are wide-spread in
the social insects and elicit a variety of
responses, such as excitement, flight,
attraction, and attack. Probably more
of these compounds have been identified
than of any other type of pheromone,
but in many cases the function of the
individual compounds has not been
elucidated, and all the components found
in an alarm secretion may not necessarily
be pheromones. Like most trail phero-
mones, alarm pheromones are short-
lasting in their effects and act only over
short distances. These properties are
reflected in their molecular size. To act
rapidly and be dissipated equally rapidly,
these compounds must be relatively vola-
tile, and most alarm pheromones have
molecular weights between 100 and 200
(Wilson, 1970), with 5—12 carbon atoms;
they include hydrocarbons, ketones,
aldehydes, and esters. There is much
less species specificity in alarm phero-
mones than in other pheromones and
sometimes several species respond to the
same alarm pheromone. This is not sur-
prising, for a threat to one insect often
threatens others also. Unlike other
pheromones, which are usually present
only in trace amounts, alarm phero-
mones are often present in fairly high
concentrations.
Responses to alarm pheromones are
many and varied. Often insects are at-
tracted by low concentrations. At higher
concentrations, response is related in
large part to the organization of the
colony. With semisocial insects such as
the bed bug, Cimex lectularius L.,
(Levinson et al., 1974) or with ants that
live in small, loosely-organized colonies
(Regnier and Wilson, 1969) in places
like rotting logs, the alarm pheromones
act as an early warning signal for evacua-
tion and they scatter in all directions.
These insects are not well-equipped for
defense, and flight is the only practical
strategy for them. For other ants in
tightly organized colonies, increasing
concentrations of the alarm pheromone
stimulate the insects to attack. The red
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
harvester ant, Pogonomyrmex barbatus
(F. Smith), is one of these. Workers of
this species will attack a wad of cotton
treated with 4-methyl-3-heptanone, a
component of its alarm pheromone, and
when a small drop of this compound
was placed on one of the ants, it was
immediately chased and attacked by
near-by nest mates (McGurk ef al.,
1966). Longer exposure to this phero-
mone brings on still another reaction, that
of digging and carrying away pebbles.
It has been suggested, but not proven,
that this is because the pheromone also
acts as a signal to rescue nest mates
buried in a cave-in.
The pheromones I have discussed so
far—sex pheromones, trail pheromones,
and alarm pheromones—are the ones
with which we are most familiar, but
pheromones with many other actions are
known.
Miscellaneous Pheromones
There are oviposition pheromones, for
example. Some mosquito larvae give off a
substance stimulating oviposition by
the adult females (Kalpage and Brust,
1973). The advantage of this is clear; a
location where eggs have successfully
hatched has proven its suitability, while
an untried pool may be only temporary
and may dry up before eggs laid there
can hatch. This pheromone would be
an example of an oviposition-stimulat-
ing pheromone. Oviposition-deterrent
pheromones are also known. After laying
an egg, female black cherry fruit flies,
Rhagoletis fausta (Osten Sacken), or
apple maggot flies, Rhagoletis pomonella
(Walsh), drag their ovipositors about the
fruit and deposit a substance that dis-
courages other females from laying in
the same fruit (Prokopy, 1972, 1975).
Some parasitic wasps similarly mark
host eggs or larvae in which they have
laid eggs (Vinson and Guillot, 1972;
Guillot et al., 1974). By preventing over-
parasitization, this gives the parasite
larvae a chance to develop without com-
petition.
The mixture of fatty acids given off
by some dead ants can also be regarded
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
as a pheromone (Wilson et al., 1958).
These fatty acids act as a signal to the
workers to carry the dead ant out of the
nest and put it onto the refuse pile. A
live ant that has been daubed with some
of these chemicals receives exactly the
same treatment. No matter how often it
returns to its nest, it gets carried back to
the dump; the process is repeated over
and over, and the hapless ant isn’t
allowed to remain in its nest until the
‘‘odor of death’’ finally wears off.
Other pheromones are involved in nest
and colony recognition (Hubbard, 1974),
brood tending (Glancey et al., 1970;
Bigley and Vinson, 1975), thermoregula-
tion (Ishay, 1972), and a host of other
phases of insect life.
There is even evidence for a ‘‘canni-
balism pheromone’’ that causes diploid
honey bee larvae to be eaten by the
workers (Dietz and Lovins, 1975). The
pheromones considered thus far have all
been ‘‘releaser’’ pheromones—they
bring about an immediate release of some
action in the receiver. Another group of
pheromones are the ‘“‘primer’’ phero-
mones that trigger a physiological change
in the receiving insect. The result of such
a change is particularly noticeable in the
desert locust, Schistocerca gregaria
(Forskal), and other locusts. In dry years
these insects resemble ordinary green
grasshoppers and tend to remain solitary,
poking around for food by themselves.
The rains of wet years, however, stimu-
late hatching of eggs in large numbers,
and it seems (Gillett, 1975; Nolte et al.,
1973) that a gregarization pheromone
excreted by the young hoppers accumu-
lates in large enough quantities to stimu-
late a color change from green to yellow
and black and a change in habit from
preferring a solitary existence to be-
coming part of a devasting swarm.
Among other primer pheromones are
ones that control caste changes in ter-
mites (Liischer, 1961; Nagin, 1972) or pre-
vent development of a new queen bee as
long as there is an active queen in the
hive (Butler et al., 1961). Some of the
various functions of pheromones are
summarized in Table I.
23
Table I.—Insect pheromones.
Sex Pheromones
Attractants
Inhibitors
Stimulants
Aphrodisiacs
Aggregation Pheromones
Trail Pheromones
Alarm Pheromones
Others
Oviposition stimulant
Oviposition deterrent
Territorial marking
Brood tending
Necrophoric
Colony recognition
Thermoregulation
Caste determination
Inhibition of queen rearing
Allelochemics
Up to this point we have been con-
sidering pheromones—chemicals used
by insects for communication with other
members of their own species. Insects
also employ other semiochemicals, the
allomones and the kairomones. With
these materials, communication is inter-
specific—between members of different
species. It should be remembered that
these classifications are for convenience
and are not exclusive. A pheromone can
also be an allomone or a kairomone.
Allomones
Allomones, by definition, are interspe-
cific semiochemicals that evoke a reaction
that benefits the emitting organism in
some way. By way of illustration, let
us consider some slave-maker ants. At
least thirty-five species of ant are known
to depend to some extent on slave labor
by other ants (Wilson, 1975a). Slave-
maker workers raid a nest of another
species and capture worker pupae, which
they carry back to their own nest.
When adults emerge from these captured
pupae, they accept their new home and
instinctively carry on the necessary
housekeeping tasks—foraging for food,
tidying the nest, and caring for the eggs
and larvae of their captors. Some slave-
makers rely on brute force in their raids
and kill resisting workers to capture the
24
pupae they are after. A few species
have been found to be more subtle. Work-
ers of Formica subintegra Emery and F.
pergandei Emery have enlarged glands
that contain relatively enormous amounts
(up to 10% of the entire body weight) of
three esters—decy]l acetate, dodecyl ace-
tate, and tetradecyl acetate (Regnier
and Wilson, 1971). These compounds are
effective alarm pheromones. A_ small
amount of an applicator stick poked into
the edge of a nest of this species caused
the entire colony to become highly ex-
cited and attracted most of the workers,
who tried to attack the stick. These same
esters also cause alarm in the nests of
ants that are used as slaves. In this case,
however, the result is panic; when the
raider ants discharge these compounds,
the excited workers run about aimlessly
and scatter in all directions, leaving the
nest free for the raiders to get the pupae
they are seeking. The scattered ants do
not return to their nest, probably because
the odors of these esters, which are
less volatile that most alarm substances,
remain around the area for a long time.
These three esters, then, act both as
alarm pheromones, summoning raiding
workers to the attack, and also as allo-
mones, producing a reaction of panic in
the attacked species that aids the at-
tackers.
Many of the defensive secretions used
by insects for their protection can be
regarded as allomones. These secretions,
which an insect emits when it is dis-
turbed, to protect itself from predators,
come in many forms—a fine spray or
jet, a slow ooze, or even a foam (Eisner,
1970). A great variety of chemicals have
been identified as defensive compounds
(Weatherston and Percy, 1970), includ-
ing aliphatic acids, esters, aldehydes,
ketones, hydrocarbons, quinones, ster-
oids, and terpenoid compounds. Most
defensive secretions contain several dif-
ferent compounds; analysis of the secre-
tion from a tenebrionid beetle showed the
presence of more than fifty compounds
(Tschinkel, 1975). Some compounds are
irritants or repellents, others are dis-
tasteful to attackers, and others appear
J. WASH. ACAD. SCI., VOL. 67, NO. 1, -1977
to make the secretion more effective by
increasing spreading or penetration.
(Venoms and other toxicants from insect
stings or bites are not generally classed
as defensive secretions.) Defensive ma-
terials may act as repellents or irritants,
or they may set up into a sticky material
that interferes with the predator’s ac-
tions. Some bombardier beetles use a
reaction much like that involved in an
aerosol can of hot shaving lather (Ane-
shansley et al., 1969). A hydroquinone
reacts with hydrogen peroxide and the
hot reaction products are sprayed out asa
fine mist that reaches temperatures of
100°C. The benzoquinones in the reac-
tion mixture are strong irritants, so the
result is both chemical and thermal heat.
A well-known defensive secretion is
formic acid, which gets its name from its
occurrence in a number of formicine ants,
where it was first reported (though mis-
identified) in 1670 (Wray, 1670). It is
found in many insect species; in some it
may also serve as an alarm pheromone.
Many other alarm secretions are also
defensive secretions, rallying attackers
as well as acting as a repellent to in-
vaders.
Some predators have learned to cir-
cumvent the defensive spray of their in-
sect prey. Grasshopper mice have been
observed to subdue beetles that spray
irritating quinones from a gland in the
abdominal tip by holding them head-up
so all the secretion is ejected onto the
ground (Eisner et al., 1963). The mouse
can then eat the beetle with impunity.
The defensive spray of some insects
contains hydrocarbons such as undecane
that may function by interfering with
chemoreceptors on the predators’ an-
tennae (Blum and Brand, 1972). Insects
often rely on their antennae to locate
their prey, and if the prey insect can
disable these antennae, it has a good
change of getting away.
A defensive chemical need not be
aimed at the predator directly. A Brazil-
lan wasp suspends its small paper nest
by a narrow stem, 2—3 cm. long. Wasp
larvae are very attractive to ants, but the
adult wasps smear the suspending stem
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
of the nest with a repellent substance
that foraging ants will not pass (Jeanne,
1970). With this protective barrier, the
larvae are safe in the nest, and the adults
need not leave a wasp on guard while
they are away.
Although the viscous or sticky ma-
terials in defensive secretions might be
regarded as being a mechanical rather
than a chemical defense, the repellent
and irritant components are clearly allo-
mones; they are chemicals conveying a
message that is of benefit to the emitter.
Flower scents may attract insects in
search of nectar. In gathering the
nectar, the insect picks up pollen, which
it then brushes off onto other flowers.
The flower scents are therefore allo-
mones, because the action elicited by the
scent results in pollination of the flowers.
Some Mediterranean orchids have a
different twist (Kullenberg, 1961, 1973).
Their scent appears to contain some of
the same compounds that are in the fe-
male sex pheromone of certain wasps.
The flowers themselves look enough like
wasps to fool males attracted and stimu-
lated by the scent, and in attempting to
mate, the males are brushed by the
pollinia and unwittingly act as pollen
Carriers.
Kairomones
Unlike the allomones, kairomones
carry a message that results in benefit to
the receiver of the message, rather than
the emitter. Often these are scents used
by parasites or predators to find suitable
prey (Vinson, 1976). Relatively few in-
sect kairomones have been identified
thus far; these include a number of hydro-
carbons that stimulate host-seeking be-
havior by various parasites of the corn
earworm, Heliothis zea (Boddie) (Jones
et al., 1971, 1973). Heptanoic acid in the
frass from potato tuberworm, Phthori-
maea operculella (Zeller), larvae is
another; it elicits heightened searching
behavior by a parasitic wasp (Hendry
et al., 1973).
Lactic acid in human sweat is one of
the cues used by some mosquitoes to
locate someone to bite (Acree et al.,
25
1968). It therefore would also be con-
sidered a kairomone.
Codling moth, Laspeyresia pomonella
(L.), larvae are attracted by a substance
found in apple skins, a-farnesene (3,7,11-
trimethyl - 1,3,6,10 - dodecatetraene)
(Sutherland and Hutchins, 1972). This
same compound stimulates oviposition
by adult female codling moths (Wearing
and Hutchins, 1973). Thus, it seems to
ensure that eggs are laid where the
hatching larvae will find suitable food.
Other oviposition stimulants in plants are
known. Allyl isothiocyanate, found in
cabbages and similar plants, stimulates.
oviposition by some insects (Gupta and
Thorsteinson, 1960; Traynier, 1965).
Certain glucosides from olives stimulate
oviposition by the olive fruit fly, Dacus
oleae (Gmelin) (Girolami et al., 1975),
but if the olives are damaged, a sub-
stance in the olive juice acts as a re-
pellent, thus preventing eggs from being
laid where chances of hatching are re-
duced. The glucosides can stimulate the
females to lay eggs in molded paper
mounds where they are easily accessible;
they may thus simplify mass rearing of
the fly.
Another substance of plant origin, not
yet identified, aids a larval parasite of
the artichoke plume moth, Platyptilia
carduidactyla (Riley), (Bragg, 1974) in lo-
cating its host. A substance in the sap
of artichoke plants that have fresh
wounds such as might be made by the
moth larvae attracts this parasitic wasp
and stimulates it in its search for its larval
host. This material illustrates again the
overlapping that may be encountered in
classification. Since the artichoke plants
are benefitted by parasitization of the
larvae feeding on them, the material is
an allomone. On the other hand, it aids
a parasite in locating its prey and acts
as a kairomone.
Polyphemus moths, Antheraea poly-
phemus (Cramer), will not mate unless
oak leaves are present. The reason for
this puzzling observation was traced
to a volatile compound, (£)-2-hexenal,
given off by the leaves (Riddiford, 1967).
Female moths will not ‘‘call’ and release
26
their attractant pheromone in the ab-
sence of this compound, and males will
not mate unless the females ‘‘call’’. Ac-
cordingly, there is no mating unless suit-
able larval food is available in the form
of oak leaves. (£)-2-Hexenal is therefore
a kairomone. Interestingly, this aldehyde
is found in the defensive secretions of a
number of insects; in the secretion of
some cockroaches, the compound is suf-
ficiently pure to induce moth mating even
in the absence of oak leaves (Riddiford,
1967).
Up to this point I have given a brief
run-down on a few of the myriad ways
in which chemicals are involved in the
interaction of insects with their sur-
roundings. In interactions between in-
sects and man, man often comes out
the loser. Insects are often vectors of
disease. Besides being painful, some in-
sect stings can cause dangerous allergic
reactions. Insects can destroy valuable
trees, make damaging inroads on farm-
ers’ crops, and consume a large por-
tion of the harvest when it is in storage.
To cut down on insect depredations, man
uses a varied arsenal of weapons, among
which are the semiochemicals. As we
reduce our reliance on pesticides, we will
have to rely more on alternative methods
of control and find new ways of using
non-toxic chemicals such as these chemi-
cal messengers.
Synthetic Materials
One approach has been to search
for effective repellents and attractants
by empirical screening of chemicals
(Beroza, 1970). A large number of com-
pounds are tested for activity; other com-
pounds related to those showing some ac-
tivity are then synthesized and tested.
By following leads in this way, we
eventually may come across a compound
with sufficient activity to have practical
applications. Deet, N,N-diethyl-m-tolu-
amide, the most effective repellent for
mosquitoes and biting flies that we have
up to now, was found in this way (Mc-
Cabe et al., 1954). Effective attractants
for a number of insects, including the
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
Japanese beetle, Popillia japonica New-
man (McGovern et al., 1970), the Medi-
terranean fruit fly, Ceratitis capitata
(Wiedemann) (Beroza et al., 1961), and
some yellowjacket wasps (Davis et al.,
1972), have also been developed by this
route. These synthetic attractants do
not occur naturally in the insects, al-
though methyl eugenol, the oriental fruit
fly, Dacus dorsalis Hendel, attractant
(Steiner, 1952), has been found in some
leaves and flowers (Kawano, 1968; Flet-
cher et al., 1975). Concentrations of these
synthetic lures that are needed for attrac-
tion are much greater than those for the
attractant pheromones. For example,
traps for the Mediterranean fruit fly
are usually baited with over a gram of
trimedlure (tert-butyl 4(or 5)-chloro-2-
methylcyclohexanecarboxylate) (Howell
et al., 1975), while amounts of the gypsy
moth pheromone used in survey traps
have ranged from 10 wg to 10 mg, and
traps baited with 1 ng of this pheromone
have caught moths even after 3 months
exposure (Beroza et al., 1971).
Applications
As we have seen, chemicals that affect
insect behavior at many stages in their
development are now known, and as
analytical methodology improves, addi-
tional compounds are being reported with
increasing frequency. The question now
is, “How can we use these compounds?”’
An obvious use of attractants is in
traps, which I have mentioned already.
Baited with attractant pheromones or
synthetic lures, these have become an
indispensable tool in surveys to locate
new insect infestations, to estimate the
size of existing infestations, to determine
the most effective timing for application
of control measures, and to check on the
effectiveness of these controls. Last
year, for example, 17,000 traps baited
with attractants for three fruit flies were
deployed around various southern ports
of entry to guard against importation of
these flies. Last fall a few Mediterranean
fruit flies were found in these traps in
one county in California (Anon., 1975),
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
and control measures were quickly in-
itiated to prevent the spread of the in-
cipient infestation. Thousands of other
traps for the gypsy moth, the Japanese
beetle, pink bollworm, Pectinophora
gossypiella (Saunders), and other insects
are being used similarly in surveys for
these pests.
Design of an effective trap is a research
project in itself (e.g., Kennedy, 1975).
Each insect has its own behavioral idio-
syncracies that must be taken into ac-
count. Factors such as trap color, trap
height, trap shape, size and position of
trap entrance, and location of lure must
all be considered. The trapping agents
may be mechanical baffles or sticky
materials that prevent escape, water or
another liquid that drowns the insects, a
toxicant, or an electrocutor grid. All in
all, traps come in a bewildering array of
sizes and shapes.
Theoretically, it should be possible to
control small insect infestations by put-
ting out traps in sufficient numbers. Up to
now, however, this has not proved practi-
cal. With the sex attractant traps, for
example, only adults, and only those of
one sex, are caught. (Boll weevil phero-
mone traps are exceptions, since the sex
pheromone also acts as an aggregation
pheromone and males as well as females
are trapped.) Since it is usually the larvae
that do the damage to the crops, reliance
on these traps for immediate crop pro-
tection would be something like locking
the barn door after the horse had been
stolen. Nevertheless, trapping of adults
will cause a reduction in the next genera-
tion, provided that there is no migration
into the area. Promising results have been
obtained in some trapping tests (e.g.,
Berozaet al., 1973b; Trammel et al., 1974)
and mass trapping may eventually de-
velop into a feasible procedure. Tests are
now underway with several insects.
A related application is the use of
pheromones to attract insects to insecti-
cide-treated trap crop plots; this proce-
dure was effective in tests against the
boll weevil (Scott et al., 1974; Hardee et
als, 1975).
At the present it appears that mating
27
disruption by general dissemination of a
sex pheromone thoughout an area will be
developed into a practical means of con-
trol more rapidly than trapping methods.
Results in tests with a number of insects
have been promising (e.g., Beroza, 1976;
Roelofs et al., 1976; Shorey et al., 1976;
Tumlinson et al., 1976; Rothschild,
1975). Last summer, for example, a
microencapsulated formulation of the
gypsy moth pheromone was sprayed over
75 square miles in northeastern Maryland
at a rate of 6 g/acre, with the result
that mating of female gypsy moths was
reduced by about 70% in the treated area.
The mechanism behind such mating dis-
ruption is not yet clear. Perhaps the per-
vasive pheromone overloads the chemo-
receptors in the males’ antennae so that
they no longer detect the females’ phero-
mone; perhaps the concentration of the
synthetic pheromone is high enough to
mask the odor trails leading to individual
females. It is quite possible that different
mechanisms may be involved with differ-
ent species. Pheromones affecting other
phases of the mating process may be
even more effective than the attractant
pheromones with some insects, and in
some cases compounds that are not
pheromones may also act as mating dis-
ruptants. Air permeation with attractant
inhibitors has disrupted mating of the
European corn borer (Klun et al., 1975)
and the redbanded leafroller, Argyro-
taenia velutinana (Walker), but dis-
semination of inhibitors has been in-
effective with several other insects. This
is an area where we have much to learn.
Trapping and mating disruption are but
two potential applications of phero-
mones. As our knowledge increases, we
should expect to find other ways of
manipulating insects with their own
chemical communication systems. For
example, the aphid alarm pheromone,
B-farnesene (7,11-dimethyl-3-methylene-
1,6,10-dodecatriene), which is given off
when an aphid is attacked, causes other
aphids feeding nearby to drop off the
plants as a way of rapid escape; it has
been suggested that this behavior might
be utilized for aphid control (Bowers
28
et al., 1972). Another type of pheromone
with potential utility for insect manage-
ment is the oviposition marking phero-
mone that deters repeated oviposition
(Prokopy, 1972: Yamamoto, 1975); field
application of partially purified phero-
mone produced by female Rhagoletis
cerasi (L.) reduced infestation of treated
cherries by nearly 80% (Katsoyannos and
Boller, 1976). The brood-tending phero-
mone of the imported fire ant, Solenopsis
invicta Buren, is still another prospect
for use in control. Filter paper discs
treated with the pheromone were rapidly
carried into the nest by workers and
treated as pupae; the pheromone may
thus provide a means of introducing and
localizing insecticide treatments within
a colony (Bigley and Vinson, 1975).
Applications of other semiochemicals
are also being explored. Release of para-
sitic wasps is proving to be one way of
reducing corn earworm, Heliothis zea
(Boddie) populations; in small field
tests, distribution of kairomones of the
corn earworm that stimulate host search-
ing by Trichogramma spp. resulted in
more even distribution of the released
parasites and less dispersal away from
the treated area (Lewis et al., 1975;
Jones et al., 1976).
From all appearances, semiochemicals
will prove to be most effective in com-
bination with other methods of insect
control. Attractants may be used to
bring insects to an area where they can
be killed with a toxicant or treated with a
pathogen or a chemosterilant. Destruc-
tion of palm trees in Samoa was reduced
by infecting the coconut rhinoceros
beetle, Oryctes rhinoceros (L.) popula-
tion with a virus with the aid of traps
baited with a synthetic lure (P. A. Maddi-
son, personal communication), and some
beetles infesting granaries have been
inoculated with a protozoan infection by
means of a pheromone-baited device
(Schwalbe et al., 1974).
A pilot test against the boll weevil
has demonstrated the potential of inte-
grated insect management through co-
ordination of various suppression tech-
niques, including the use of pheromones
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
(Hedin et al., 1976). Late season insecti-
cide treatments were used to reduce
overwintering weevil populations. Re-
moval of cotton plants after harvest
destroyed food and shelter to cut down
chances of survival of weevils that es-
caped the insecticide. Pheromone traps
were used for monitoring throughout the
test and were set out in the spring to
catch emerging weevils. The release of
male weevils treated with a chemo-
sterilant dealt the final blow by ensuring
that any surviving females would pro-
duce only infertile eggs. Despite some
migration of weevils into the treated
area from infested fields outside, the two-
year program effectively eliminated the
weevil from two-thirds of the experi-
mental area.
As we learn more about insect semio-
chemicals and their behavioral effects,
we can expect to find many new and
imaginative ways of using them in insect
management programs.
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33
RESEARCH REPORTS
Biological Notes on Stenodynerus microstictus
(Hymenoptera: Eumenidae)
John M. Hackney and Edward M. Barrows!
Department of Zoology, University of Queensland, St. Lucia, Brisbane, Australia
4067; and Department of Biology, Georgetown University, 37th & O Streets, N.W..,
Washington, D. C. 20057, respectively
ABSTRACT
The turret-building wasp, Stenodynerus microstictus, is active from May to October
in northeastern Kansas and has aggregated nests in vertical river banks. Nests
contain 1 to 17 brood cells provisioned with noctuid and gelechiid larvae. S.
microstictus, reared in the laboratory, developed from an egg to an adult in about
19 days. Trypoxylon sp. (Sphecidae) uses abandoned nests of this eumenid as nesting
sites.
Stenodynerus microstictus (Viereck),
which constructs a ‘“‘lacelike’’ nest turret
(Fig. 1), has received limited treatment
in the literature. Evans (1956) briefly ex-
amined its nest architecture and provi-
sions in Pottawatomie County, Kansas,
citing similarities to Isley’s (1914) ob-
servations of the related species S. papa-
gorum (Viereck). We relate further
aspects of the biology of S. microstictus.
Methods
Observations were made from May to
September, 1974, on the banks of the
Kansas River, 14.5 km east of Lawrence,
Douglas County, Kansas. In most cases,
nests in lumps of soil were examined in
the laboratory. Bleached flour was
squeezed from a plastic bottle into nests
to facilitate finding burrows in soil and
cell provisions were preserved in
1 Reprint requests should be sent to E. M.
Barrows, Georgetown University.
34
Dietrich’s (Kahle’s) solution. Immature
wasps selected for rearing were placed
with cell provisions in vials closed with
cotton plugs and held in darkness at
room temperature.
Results
S. microstictus is active about nests
from early May to early October (W. A.
Hawkins, pers. comm.). Wasps begin
leaving nests when direct sunlight first
illuminates nesting sites (0900, August).
One wasp observed during the entire
period of activity outside the nest, left
and returned to her nest 5S times in 1
day. She stayed away from her nest from
85 sec to several hours and her activity
outside the nest ceased just before sun-
set, 1850.
The 19 nests which were studied were
‘loosely aggregated’’ in about 10 m? of
vertical river bank 2.5 m high that faced
northwest. A 50-cm bank overhang shel-
tered the nests, the burrow entrance of
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
Fig. 1. Nest turret of Stenodynerus microstictus. Fig. 2. Female S. microstictus constructing
a nest turret (photograph from a color slide taken by W. A. Hawkins).
each being within an indentation in the
bank’s hard, sandy soil. Nest entrances
averaged 1.0 m below the top of the bank
(range, 0.3 to 2.0 m; n = 12); the mean
distance between nests was 12.5 cm
(range, 2 to 100 cm; n = 12). Eight of the
19 nests were actively inhabited. The
nearest other aggregation was about 40 m
upstream. Nests of S. microstictus were
dispersed among nests of other hymenop-
terans including Lasioglossum (Dialic-
tus) zephyrum (Smith) (Halictidae), Phi-
lanthus gibbosus (Fabricius) (Spheci-
dae), and Hylaeus binsinuatus (Forster)
(Colletidae) (Barrows, 1975).
Aspects of nest construction by 3
wasps nesting within 1 m? were ob-
served. In constructing her nest, a wasp
Carries small bits of moistened soil with
both her mouthparts and forelegs as she
backs out of her burrow. She affixes
soil to the rim of the burrow entrance
with mouthparts alone, her legs sup-
porting her at first on the bank and later
on a lengthening turret (Fig. 2). As turret
construction progresses, her abdomen
curves up and behind the wall of the turret
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
as a support against which soil bits are
tamped into a rough lacework. During
construction the wasp periodically
backed into the turret and appeared to
rest there for about 40 sec, entered the
burrow for an average of 15 sec (range
5 to 20 sec; n= 27), or cleaned her-
self before flying towards the river (possi-
bly to collect water), remaining away an
average of 8 min (range, 2 to 10 min;
n= 5). We observed that all excavated
soil was used in turret construction;
however, some soil which S. microstictus
removes in digging burrows might be
simply dumped out of the nest. Turrets
are too short to be composed of all the
soil excavated from nests.
Twice, other conspecific wasps _at-
tempted entering nests while wasps con-
structed turrets. This resulted in heated
battles; the wasps fell to the foot of the
bank biting and attempting to sting one
another.
Provisions from 7 cells are listed in
Table 1. About 35% of the provisions
were desiccated. Larval miltogrammine
sarcophagid flies were found among wasp
35
Table I.—Contents of cells of Stenodynerus microstictus.
Cell No. Contents
1 Diptera: Calliphoridae: possibly Phaenicia sericata (Mg.)', 1 larva
Hymenoptera’, 1 egg
Hymenoptera: Aculeata: probably Sphecidae?, 2 larvae
Lepidoptera: Noctuidae: Charcoma nilotica (Rogenhofer)*, 2 larvae
Lepidoptera’, 4 eggs
2 Lepidoptera: Noctuidae: C. nilotica, 5 larvae
3 Lepidoptera: Noctuidae: C. nilotica, 3 larvae, 1 prepupa, 1 pupa
4 Hymenoptera: probably Sphecidae?, 11 larvae
Lepidoptera: Noctuidae: C. nilotica, 7 larvae, 1 prepupa
>) Hymenoptera’, 1 prepupa
6 Lepidoptera: Noctuidae: C. nilotica, 6 larvae
i Coleoptera: Curculionidae: Ceuterhychinae: near Auleutes*, 3 larvae
Lepidoptera: Gelechiidae’, 2 larvae
1 Determined by R.J. Gagné
2 Determined by A.S. Menke
3 Determined by D.M. Weisman
* Determined by D.M. Anderson
provisions. It is unclear whether these
flies were parasites of the wasps or of
the provisions and why calliphorids,
sphecids, and curculionids were found in
cells of S. microstictus.
Life cycle information is limited due to
63% mortality of S. microstictus im-
matures. Five were reared from larvae,
with a maximum of 7 days spent in that
life stage. The pupal stage lasted an
average of 11.8 days (range, 9 to 14
days; n= 6). One male wasp was reared
to adulthood from an egg of unknown
age. It was an egg for 1 day; a larva,
6 days; a prepupa, | day; and a pupa,
11 days.
Some nests were more complex than
those examined by Evans, although many
had only 1 or 2 cells (Figs. 3, 4). On
the average there were 4 cells per nest
(range, | to 17 cells; n = 20 nests), with
a mean cell length of 1.3 cm (range, 0.7 to
lS em; n= s80cells) and 0.5 cm in
greatest diameter (range, 0.45 to 0.50
cm), tapering to 0.4 cm at either end.
Most cell walls were coated with a thin,
‘‘silky,’’ shiny substance. Cells were
separated by thin soil partitions and were
often in a series of 2 or 3. In the more
complex “nests” (Fig. 5), ‘cells™ were
36
bunched along either side of the burrow,
while simpler nests had them gathered
only at the burrow’s distal end. Distance
from nest entrance to cells ranged from
0.5 to 12.0 cm. Burrow length averaged
5.7 cm (range, 2.0 to 12.0 cm, n= 20),
the mean diameter being 0.4 cm (range,
0.35 to 0.4 cm). Burrows penetrated the
bank more or less perpendicularly. The
turrets shared the burrows’ average diam-
eter of 0.4 cm (range, 0.4 to 0.5 cm,
n= 16) with mean length of 1.5 cm
(range, 0.3 to 4.0 cm). Erosion probably
decreased turret lengths because many
had jagged ends. Two inhabited nests
completely lost turrets.
Nest provisioning was observed at
1130. A female flew towards a nest
entrance clenching an 8-mm caterpillar
with her forelegs. After landing upon the
turret, she used her fore- and middle
legs to push the prey ahead as she ad-
vanced into the nest, bracing herself with
her hind legs pressed against the turret’s
interior.
A Trypoxylon wasp landed upon a tur-
ret at 1530, August 20, chewed its outer
surface near the proximal end for 30 min,
and gained an opening large enough for
entrance. The wasp was active inside
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
the nest from 1630 to 1930 (dusk),
frequently returning to the new opening
to dump soil bits or make short flights.
Excavation of this abandoned S. micro-
stictus nest made 2 days later revealed
that 1 cell contained an egg and 23
spiders. The egg was reared until death
at the prepupal stage, which prevented
a species identification. Hawkins (pers.
comm.) reared Trypoxylon sp. from nests
of S. microstictus at the same site.
Olberg (1959) disclaims a hypothesis of
turret building as a deterrent to parasites
or “‘invaders’’, citing the frequent oc-
currence of both in the turreted euminine
nests of his studies. The evidence here
indicates the turret posed a barrier for
the invading Trypoxylon, although
further work is needed to evaluate ef-
fectiveness in this or other capacities.
Acknowledgments
We thank W. A. Hawkins and C. D.
Michener (University of Kansas), G.
Gordh (Syst. Entomol. Lab., Agr. Res.
Serv., USDA) and Jai Guru Dev (Uni-
versity of Queensland) for their construc-
tive advice. Identifications were grate-
fully received from D. M. Anderson,
R. J. Gagné, A. S. Menke, and D. M.
Weisman (Syst. Entomol. Lab., Agr.
Res. Serv., USDA). R. M. Bohart
(University of California at Davis) identi-
fied Stenodynerus microstictus. This
study was made when both authors were
at the University of Kansas and is in
part a byproduct of National Science
Foundation Grant GB-38502 (W. J. Bell
and C. D. Michener, Coprincipal in-
vestigators).
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
’ ae
eae I
Bee !
ae 1
.
PES -
3
ij A
\
\
\ HW Ache
\ ’ \
\ 1 \
> N
4 A ~
mod S-
\
! \
\
\ y
\ 1
\ ! 1
SS) meee ene
Figs. 3-5. Side views of nests of Stenodynerus
microstictus: B, burrow; C, cell; P, plug of soil;
S, surface of vertical river bank; T, turret.
References Cited
Barrows, E. M. 1975. Occupancy by Aylaeus
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Olberg, von G. 1959. Das Verhalten Der
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Verlag Der Wissenschaften, Berlin. 402 pp.
37
A Review of Pseudorhizoecus Green, with a Description
of a Related New Genus (Homoptera: Pseudococcidae)
Edson J. Hambleton
Cooperating Scientist, Systematic Entomology Laboratory, IIBIII, ARS, USDA.
Mail Address: 5140 Worthington Dr., Washington, D. C. 20016
ABSTRACT
The genus Pseudorhizoecus Green and its type-species proximus are redescribed;
a lectotype is designated, and the diagnostic characters of P. proximus are figured.
A new genus Capitisetella is proposed for Pseudorhizoecus migrans Green because
the species has several features not known on P. proximus. A redescription of C.
migrans is given and its diagnostic characters are illustrated.
Green (1933) described the genus
Pseudorhizoecus for the new species
proximus and migrans from Surinam
(Dutch Guiana). Green considered the
genus to be assignable to the Pseudo-
coccidae and characterized it by the ab-
sence of both anal-ring setae and *‘beaded
or areolated’’ structures present on the
anal ring of related genera. After careful
examination of all available material of
P. proximus and P. migrans, including
the types, I have found that both species
have anal-ring setae. In the type-species,
P. proximus, the anal ring has an incon-
sistent number of small setae and many
isolated protuberances, many of which
have apical spicules. In P. migrans the
anal ring is very different; it has 6 ob-
vious setae that are relatively consistent
in size and location, and it lacks the
protuberances found on P. proximus.
Based on these differences and on char-
acteristics of the antennae, leg spines,
and body setae it is evident that proximus
and migrans should be placed in different
genera.
Genus Pseudorhizoecus Green
Pseudorhizoecus Green, 1933:55. Type-species:
Pseudorhizoecus proximus Green, by original
designation.
Body of female robust, about 1 mm. long. An-
tennae 5-segmented, weakly geniculate, terminal
segment with slender, curved sensory setae. Eyes
absent. Anal-lobe area undeveloped, without dif-
38
ferentiating setae or sclerotization. Anal ring with
few indiscriminately placed small setae, several
cells and many oval protuberances. Legs with
characteristic tibial and tarsal spines. Derm with
crowded, slender, apically acute setae arranged in
bands across segments, with few trilocular pores.
Adult male apterous, with 5-segmented antennae
similar to female. Eyes absent. Legs well de-
veloped. Penial sheath and aedeagus strongly
sclerotized, superficially resembling Rhizoecus.
Derm with setae crowded in bands across seg-
ments as in female.
Discussion.—For a comparison of
Pseudorhizoecus with the new genus
Capitisetella see ‘Discussion’? under
that genus.
Pseudcrhizoecus proximus Green
Fig. 1-3
Pseudorhizoecus proximus Green, 1933:55.
Adult female: Broadly ovate. Length, 0.85—95
mm; width, 0.75—0.88 mm. Antennae closely
spaced, moderately short, stout, tapering toward
apex, average length of segments in microns: I,
28; II, 17; III, 14; IV, 11; V, 46; apical segment
about 2 times as long as wide, with 4 very slender
and 2 short sensory setae; all segments with
numerous long, apically acute setae. Interantennal
space less than width of segment I. Rostrum
moderately stout, averaging 8lu long, 55u wide;
rostral loop reaching to or slightly beyond 2nd
coxae. Cephalic plate and dorsal ostioles absent.
Legs well developed, fairly stout, elongate,
with numerous setae, average length of segments of
hind pair in microns: Trochanter, 51; femur, 111;
tibia, 99; tarsus, 45; claw, 32; tibiae each with 1
pair stout spines on ventral surface near distal
extremity; tarsi each with 2 pairs of elongate
spines on ventral surface, the distal pair more
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
Fig. 1-3, Pseudorhizoecus proximus, &:
and claw of left hind leg; 3, anal ring.
setose, reaching beyond base of claw; digitules
short, setose, not reaching half length of elongate,
weakly curved claws.
Anal ring irregularly outlined, broader than
long, about 52u wide, strongly sclerotized, without
elongate anal-ring setae but with 2—5 short setae
about 15-17 long, few cells, and 25—30 small oval
protuberances, most with short, stout spicules.
Derm without circuli, cerores, tubular ducts or
disk pores; trilocular pores more numerous on
venter of posterior abdominal segments and dor-
sally along borders of setal bands. Body setae
slender, apically acute, 15—20u long, crowded,
some longer setae occurring ventrally.
Material examined. —Five slides con-
taining 8 adult females, 2 adult males,
14 immature females, including the type
female and cotype male, all from Surinam
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
1, antennal segment V; 2, tibia, tarsus
(Dutch Guiana), on Coffea liberica,
1931-33, G. Bunzli. In British Museum
(Nat. Hist.). Since the type slide con-
tains 3 females, and no type specimen
was indicated by Mr. Green, I am desig-
nating the one ringed with ink on right
side of slide as the lectotype.
Thirty-three additional specimens in
the U. S. National Museum Collection
represent new host and distribution
records: Colombia: On Coffea arabica,
10-X-56, S. E. Flanders. Costa Rica: On
Musa paradisiaca var. sapientum, 10-V-
57, E. B. Dixon: Palmar, 24-VIII-60,
L. Roth; Turrialba, on Theobroma ca-
cao, 29-VII-56, Neal Weber. Ecuador:
39
Fig. 4-6, Capitisetella migrans, 2°: 4, terminal portion of antennal segment III; 5,
anal ring; 6, tibia, tarsus and claw of left hind leg.
Pichilingue, on coffee, 1-X-44, E. J.
Hambleton. Guatemala: Retalhulew, on
coffee, 16-V-45, E. J. Hambleton.
Capitisetella Hambleton, new genus
Type-species: Pseudorhizoecus migrans Green.
Body of female weakly pyriform, averaging
1 mm. long. Antennae 3-segmented, terminal seg-
ment with slender sensory setae. Eyes absent.
40
Anal-lobe area simple, undeveloped without dif-
ferentiating setae or sclerotization. Anal ring at
posterior apex, strongly sclerotized, with 6 regu-
larly placed, slender setae and few elongate cells.
Legs stout, with long, capitate setae but without
tarsal or tibial spines. Derm with scattered,
stout capitate setae and trilocular pores.
Adult male apterous with 3-segmented antennae
similar to female; apical segment with 20-25
slender sensory setae of different sizes, and about
as many capitate setae. Eyes absent. Legs well
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
developed. Penial sheath and aedeagus heavily
sclerotized, similar in general conformation to that
of Pseudorhizoecus. Derm with few trilocular
pores and capitate setae across segments.
Discussion. —Capitisetella, with anal-
ring setae, 3-segmented antennae, capi-
tate setae and without leg spines is easily
separated from Pseudorhizoecus. Capi-
tisetella and Pseudorhizoecus are similar
to Brevicoccus Hambleton from Brazil,
but Brevicoccus differs by having 4-seg-
mented antennae, 12—15 anal-ring setae
and multilocular disk pores. The struc-
tural arrangement of the anal ring in
Brevicoccus is similar to Rhizoecus.
The striking morphological differences
in Brevicoccus, Capitisetella and Pseu-
dorhizoecus indicate a departure from the
more characteristic rhizoecine form.
Capitisetella migrans (Green), new combination
Fig. 4-6
Pseudorhizoecus migrans Green, 193356.
Adult female: Ovate, posterior area slightly
produced. Length, 0.97—1.25 mm; width, 0.63—0.72
mm. Antennae widely spaced, average length of
segments in microns: I, 50; II, 23: III, 105;
apical segment about 3 times as long as wide,
with S—7 slender, variable, weakly falcate sensory
setae, all segments with capitate setae. Interan-
tennal space about equal to length of segment III.
Rostrum stout, about 105 long, 91 wide; rostral
loop reaching to 2nd coxae. Cephalic plate and dor-
sal ostioles apparently absent.
Legs well developed, robust, elongate, length of
segments of hind pair in microns: Trochanter,
62; femur, 116; tibia, 82; tarsus, 71; claw, 44;
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
tibiae and tarsi without spines, with capitate setae;
claws narrow, weakly curved; digitules very short,
setose, not reaching half length of claw.
Posterior abdominal area narrowed toward apex,
with no anal-lobe development or differentiating
setae. Anal ring simple, wider than long, about
504 wide with 6 slender setae about 25—28u
long; cellular structure indistinct, in preadult female
few cells visible below anterior pair of setae.
Derm setae variable in size, longest about 45y,
more abundant ventrally. Circulus, disk pores and
tubular ducts absent. Trilocular pores almost
circular in outline, more numerous than body setae,
sparse ventrally between legs and intersegmentally.
Material examined. —Holotype adult
female, 1 adult male, 8 additional fe-
males, 24 immature females, from roots
of Coffea liberica and grasses, Surinam,
1931-45, G. Bunzli. In British Museum
(Nat. Hist.). Ten additional specimens
including 2 males in process of moulting
recorded from roots of grass, Guyana
(British Guiana), R. Mazaruni, 31-VIII-
35, N. A. Weber. Colombia: On coffee,
10-X-56, S. E. Flanders; Cucuta, on
Panicum maximum, 10-VI-75, Jenner.
In U. S. National Museum.
Acknowledgment
I thank Dr. D. J. Williams, British
Museum (Natural History), London, for
the loan of type material.
Reference Cited
Green, E. E. 1933. Notes on some Coccidae from
Surinam, Dutch Guiana, with description of new
species. Stylops 2(3): 49-58.
41
Four New Species of Aegialia (s. str.) (Coleoptera:
Scarabaeidae) From California and Nevada Sand Dunes >
Robert D. Gordon and O. L. Cartwright
Systematic Entomology Laboratory, IIBITI, Agric. Res. Serv., USDA,
% U. §. National Museum, Washington, D. C. 20560; and Emeritus
Entomologist, Department of Entomology, U. S. National Museum,
Smithsonian Institution, Washington, D. C. 20560, respectively
ABSTRACT
Four new species of North American Aegialia (magnifica, crescenta, hardyi, and
concinna) are described. A key to the North American species of Aegialia (s. str.) and
illustrations of habitus, genitalia, and other morphological details are presented.
Current research on the ecology of
sand dune areas in the western United
States (principally in California and
Nevada) is being conducted by Dr. Alan
Hardy, California Department of Agri-
culture, Sacramento, and several co-
workers. Members of the Scarabaeidae
form a large segment of the beetles
associated with sand dunes; several un-
described species have been collected
including the four new Aegialia species
described here.
Many of the dune systems being stud-
ied are under pressure from recreational
and commercial interests, and the result-
ing use of the dunes often destroys
them from the natural history point of
view. Attempts are being made to have
at least some areas of these dune sys-
tems preserved, and the presence of en-
demic species is one lever that can be
used toward this end. For that reason
we are describing these 4 species of
Aegialia, each of which is apparently
restricted to a particular set of dunes.
The North American species of Aegialia
have not been studied as a whole
since Brown’s 1931 revision of the genus.
We have modified Brown’s key to spe-
cies of Aegialia (s. str.) to include the
new species described here. Brown did
not illustrate male genitalia. We have
examined the male genitalia of all de-
scribed species of Aegialia (where males
are available) and include illustrations
of those of the new species.
Brown’s (1931) classification of the
North American members of the Aegialiini
resulted in the establishment of 2 genera,
Aegialia Latreille and Micraegialia
Brown. Aegialia is divided into 4 sub-
genera: Leptaegialia Brown, Anomalae-
gialia Brown, Psammoporus Thomson,
and Aegialia (s. str.). The 4 species
described here all belong to the latter
subgenus.
All illustrations presented in this paper
were prepared by Michael Druckenbrod,
Smithsonian Staff Artist. The scanning
electron microscope time for this paper
was supported in part by the University
of Maryland Center of Materials Re-
search, Department of Mechanical En-
gineering and Electron Microscope Cen-
tral Facility, College Park, Maryland.
Key to species of North American Aegialia (s. str.)
1. Pronotum with basal marginal line strong, entirely visible (fig. 1) ............ 2
Pronotum with basal marginal line absent or interrupted (fig. 2) ............. 9
2: Hind tibial spurs:short, broad; foltaceous (fies 11). 2). 30.224. 0n ee eee 3
Hind tibial spurs slender, somewhat spatulate (fig. 9) ...............00 eee ee 6
3. Elytral striae feebly impressed, indistinct; apex of body extremely broad,
42
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
convex; hind tibia with single, longitudinal row of tubercles on inner margin;
SOUCM CMEC ANLOWMAZe Ur Mole) ciate haste eects eats oe bv oe Oe es eaee eA convexa Fall
Elytral striae distinctly impressed; apex of body not extremely broad or convex;
hind tibia with double row of tubercles; most of U. S. and southern Canada 4
4. Color pale brown to medium reddish brown ............. conferta conferta Horn
Color dank OLOWNLOMMeably DIACKS |... 5. oe Aue s ce ew ven ene bhse a ceed 5
5. Pronotum finely, sparsely punctured; length 3.4 to 3.6mm .................
I a Pe AE aie eA ac atch cn ule aes aunties nats Sa conferta nigrella Brown
Pronotum with strongly impressed, coarse punctures; length 3.6 to 4.2
EVIE Pere ha Core er UA 5 Sos seat Meas si ee RG conferta punctata Brown
6. Hind tibia without complete obliquely transverse ridges, a single longitudinal
row of small tubercles present on inner margin, outer margin with irregular,
LARC e Rt ERGleS: (iO! Oye 2 er vcs Sua se nc Rion geueleate ne Sate dws blanchardi Horn -
Hind tibia with at least one complete obliquely transverse ridge, tubercles
enimerylackine or only one or 2 present (fig. 12) ...2.... 0. nce Sete es oh
7. Color pale red; head smooth, lacking tubercles, granules or coarse punctures
CED 1) ose eas Rika ele Sar State ES ee a ORE ie eee ane e magnifica, n. sp.
Color dark brown to nearly black (except concinna); head rough, with either
caszisaapumeiiies, OF Pranules. OF DOEM...: 0.cas sees sda an sews bee seen: 8
8. Length less than 3.6 mm; color pale brownish yellow; head granulate with
Sone coarse punctures (Ne. 4) 56. Secs cee alo dase osu ce des concinna, nN. sp.
Length more than 3.7 mm; color dark brown to nearly black; head coarsely
pounced. not pranulate (ig. 2)... .. iwc ew Sue ch eee ses crescenta, N. sp.
9. Hind tibial spurs foliaceous; length 3.0 to 3.7 mm.................. opifex Horn
Hind tibial spurs slender, somewhat spatulate (fig. 13)
10. Pronotum nearly impunctate, some fine, indistinct punctures on disc
Be ss RM oe ue MOR ot oh se arenaria (F.)
eee es eee ee ee ee eee ww eee eee ee ee ee ew
We aGanct cis: d.ubewaaic eee S 10
ELOnOWMmCOAESCLY PUNCUITER 222. 6.55605 «cece ees dew ed ahve cue eens dee ue 11
11. Hind tibia with a complete, strong ridge at apical 2/3 (fig. 16) ...... hardyi, n. sp.
Hind tibia without a complete ridge, sometimes without a partial ridge....... 12
12. Pronotum densely, coarsely punctured throughout ............ latispina LeConte
Pronotum lacking punctures anteriorly and laterally, or punctures, if present,
FINALS MUICIMIMIELES INCE iia fn ee, Saou cee Sak ce tls kt aie as phos ete e ye 13
13. Pronotal punctures coarse basally, fine and indistinct apically and laterally ...
Ce
eae Meat eee crassa crassa LeConte
Pronotal punctures fine basally, apical and lateral areas impunctate..........
i
Aegialia (Aegialia) magnifica, new species
Holotype.—¢, length 5.40 mm, greatest width
2.85 mm. Form convex, oval, very broad pos-
teriorly (fig. 1). Pale red; mouthparts and ventral
surface yellowish red. Head smooth, shiny, finely
alutaceous, fine punctures separated by a diameter
or less, becoming coarser and denser at antero-
lateral angle; clypeus very feebly emarginate
medially, anterior margin evenly reflexed. Pro-
notum smooth, shiny, surface barely perceptibly
alutaceous, fine punctures separated by less than
to 3 times a diameter, lateral fovea absent;
base with marginal line distinct, entire. Elytron
smooth, shiny, punctures on intervals very fine,
separated by 2 to 5 times a diameter, intervals
flat; striae feebly impressed, finely punctured,
punctures separated by 2 times a diameter. Meta-
sternum shiny medially, becoming densely punc-
tured with intermixed fine and coarse punctures
laterally. Functional wings absent. Abdominal
Sterna densely, coarsely punctured, punctures
separated by less than a diameter; apical sternum
with elongate, median depression. Middle tibia
smooth with strong, complete ridge at basal 14, and
strong, complete ridge present medially; hind tibia
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
caper eet ee Nese scan 8 crassa insularis Brown
broad apically, with incomplete ridge at basal %,
strong, complete ridge present at apical %, sur-
face smooth with fine, indistinct punctures (fig. 12);
tibial spurs weakly spatulate (fig. 13); tarsus about
% as long as tibia. Genitalia as in fig. 5.
Allotype.—?, length 5.55 mm, greatest width
3.0 mm. Similar to holotype except apical ab-
dominal sterna without median impression.
Type-material.— Holotype, Nevada, Nye Co.,
‘*Big Dune’’, Amargosa Desert, 2500’, IV-29-1974,
Hardy & Eichlin (at light) (USNM 73838). Allo-
type, same data as for holotype (USNM). Para-
types, 348, locality same as for holotype, dates
are as follows; 12-I-1972, 11-X-1972, 17-X-1972,
20-XI-1972, 19-XII-1972, 15-I-1973, 29-III-1974,
19-IX-1974, 28-IV-1975; collectors are as follows;
F. G. Andrews and A. R. Hardy, Derham Giuliani,
Neal Rulien: ecological data available is ‘‘sifting
sand.’’ Paratypes in collection of USNM, Cali-
fornia Academy of Sciences, Alan Hardy, Neal
Rulien and Henry Howden.
Variation.— Length ranges from 4.40 to 5.90 mm,
width from 2.48 to 3.25 mm.
43
Figs. 1-4, habitus of Aegialia species. Fig. 1, A. magnifica; fig. 2, A. crescenta; fig. 3, A. hardyi;
fig. 4, A. concinna.
44 J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
Figs. 5-7, male genitalia of Aegialia species. Fig. 5, A. magnifica; fig. 6, A. crescenta; fig. 7, A. hardyi.
Remarks .—A. magnifica is the most
distinctive species of North American
Aegialia (s. str.) presently known. The
red color, usually large size, and smooth
dorsal surface are very characteristic,
and even small examples are not easily
confused with any other species. The
presence of a distinct marginal line on the
pronotal base causes magnifica to go to
the blanchardi section of the key, but
the male genitalia and hind tibiae indi-
cate a close relationship to crescenta, n.
sp., and hardyi, n. sp.
Aegialia (Aegialia) crescenta, new species
Holotype.— 6, length 4.25 mm, greatest width
2.40 mm. Form convex, oval (fig. 2). Dark reddish
brown; ventral surface, legs and mouthparts pale
yellowish brown. Head shiny, with band of coarse,
nearly contiguous punctures from basal portion of
clypeus to vertex; apical portion of clypeus less
coarsely punctured, apical margin feebly emargi-
nate medially, feebly reflexed. Pronotum smooth,
shiny, disc with indistinct, feebly impressed
furrow extending from base nearly to anterior
margin, midline narrowly impunctate, rest of pro-
notum with coarse, sparse punctures separated
by less than 1 to 3 times a diameter, feeble
lateral fovea present; base with marginal line
distinct, entire. Elytron smooth, shiny, intervals
flat, punctures on intervals in single, slightly
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
irregular, median row, separated by less than to
3 times a diameter; striae distinctly impressed,
coarsely punctured, punctures separated by a diam-
eter. Metasternum densely, finely punctured
medially, intermixed fine and coarse punctures
present laterally. Functional wings absent. Ab-
dominal sterna strongly alutaceous, densely punc-
tured; apical abdominal sternum with oval, median
depression. Middle and hind tibiae and apical
spurs as in figs. 14, 15. Genitalia as in fig. 6.
Allotype.—@, length 4.60 mm, greatest width
2.55 mm. Similar to holotype except apical ab-
dominal sternum without median depression.
Type-material.— Holotype, Nevada, Nye Co.,
Crescent Dune, 12-IJ-1976, Fred G. Andrews and
Alan R. Hardy (USNM 73839). Allotype, same
data as for holotype except date IV-24-1975
(USNM). Paratypes, 187, locality same as for
holotype, dates differ as follows; 10-II-74, v-IV-75,
24-IV-75: some collected by Derham Giuliani.
Paratypes in collections of USNM, California
Academy of Sciences, Alan Hardy, and Henry
Howden.
Variation.—Length ranges from 3.75 to 5.00
mm, width from 2.05 to 2.70 mm. The dorsal
surface is somewhat alutaceous in some specimens,
and the midline of the pronotum sometimes
lacks any trace of a longitudinal furrow and
may be sparsely punctured.
Remarks.—A. crescenta most nearly
resembles hardyi, n. sp., and it is pos-
sible that these are merely disjunct
45
Figs. 8-13, hind tibiae and spurs of Aegialia species. Figs. 8 and 9, A. blanchardi; figs. 10 and 11,
A. conferta; figs. 12, and 13, A. magnifica.
populations of a single species. However, ences (figs. 6, 7), we prefer to consider
because of the presence of a distinct them as distinct species despite the ab-
marginal line on the pronotal base of sence of intermediate populations. Of the
crescenta, the sparse pronotal punctation previously described species, latispina is
of that species, and the genitalic differ- most similar in appearance, but the hind
46 J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
Figs. 14-17, hind tibiae and spurs of Aegialia species. Figs. 14 and 15, A. crescenta; figs. 16 and
17, A. hardyi.
tibia of Jatispina is of a completely
different type than that of crescenta, as
are the male genitalia.
The specific name is a neolatin noun
referring to the type locality.
Aegialia (Aegialia) hardyi, new species
Holotype.—<¢, length 4.50 mm, greatest width
2.38 mm. Description as for crescenta except
differences noted as follows: head with vertex
punctured; pronotal punctures coarse, dense, sepa-
rated by a diameter or less, punctures present
on midline, basal marginal line not visible in dorsal
view (fig. 3), hind tibia and spurs as in figs. 16, 17:
male genitalia as in fig. 7.
Allotype.—@, length 5.10 mm, greatest width
2.60 mm. Similar to male except apical abdominal
sternum without median depression.
Type-material.— Holotype, Nevada, Churchill
Co., Sand Mountain Dunes, 16-[X-1974, Fred G.
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
Andrews and A. R. Hardy (USNM 73840).
Allotype, Nevada, Churchill Co., Sand Mountain,
13-II-1973, Derham Giuliani (CAS). Paratypes, 16,
same data as for holotype and allotype except
as follows; Nevada, Churchill Co., Sand Moun-
tain, 12 mi. S., 20 mi. E. Fallon, 28-II-1974.
Paratypes in collections of USNM, California
Academy of Sciences, and Alan Hardy.
Variation.— Length ranges from 4.33 to5.10mm,
width from 2.25 to 2.60 mm.
Remarks .—See comments under de-
scription of crescenta. A. hardyi re-
sembles latispina LeConte but the hind
tibiae of latispina are tuberculate and
lack any complete ridges. We take pleas-
ure in naming this species for Alan Hardy
in view of his active interest in the
ecology of sand dunes and his efforts
toward preserving this habitat.
47
Aegialia (Aegialia) concinna, new species
Holotype.— 2, length 3.52 mm, greatest width
1.80 mm. Form convex, elongate (fig. 4). Pale
brownish yellow, ventral surface mostly paler
than dorsum. Head mostly granulate with some
close, coarse punctures, vertex smooth; apical
margin of clypeus reflexed, barely perceptibly
emarginate medially. Pronotum smooth, shiny,
coarsely punctured, punctures separated by a di-
ameter or less; base with distinctly visible marginal
line. Elytron smooth, shiny, punctures on intervals
nearly invisible, arranged in a single irregular row;
striae deeply impressed, coarsely punctured, punc-
tures separated by twice a diameter. Metasternum
smooth, shiny medially, alutaceous with coarse punc-
tures laterally. Functional wings absent. Abdominal
sterna shiny, faintly alutaceous, finely punctured;
apical and preapical sterna fused medially. Middle
tibia slender, with a weak, incomplete ridge at
basal % and strong, complete ridge at middle;
hind tibia slender, with incomplete ridge at basal
14 and incomplete ridge at apical %4, surface
smooth, lacking punctures; tibial spurs slender,
feebly spatulate.
Type-material.— Holotype, California, Fresno
Co., 18 mi. SW Mendota, Sec. 15 T16S RI13E,
48
27-II-1975, G. Andrews, E. L. Paddock and A. J.
Gilbert collectors (USNM 73841). Paratypes, 3,
same data as for holotype. Paratypes in collec-
tions of USNM and Alan Hardy.
Variation.— Length ranges from 3.33 to 3.52 mm,
width from 1.75 to 1.80 mm.
Remarks .— The small size, pale color,
and slender, smooth hind tibiae distin-
guish concinna. No close relationship
with any known species of Aegialia
(s. str.) is apparent, and the lack of
males makes genitalic comparisons im-
possible. The presence of a completely
visible basal marginal line on the pro-
notum places concinna in the blanchardi
section of the key but there is no
phyletic significance to this association.
Reference Cited
Brown, W. J. 1931. Revision of the North
American Aegialiinae (Coleoptera). Canadian
Entomol. 63: 9-19, 42-49.
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
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Secretary:
Treasurer:
Managers-at-Large:
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
Potomac Division, American Phytopath-
ological Society ELECTED
Metropolitan Washington Chapter of the
Society for General Systems Res.
ELECTED
Potomac Chapter, Human Factors So-
ciety ELECTED
49
SCIENTISTS IN THE NEWS
Contributions in this section of your Journal are earnestly solicited.
They should be typed double-spaced and sent to the Editor three
months preceeding the issue for which they are intended.
DEPARTMENT OF THE ARMY
Helmut Sommer has received the
Army’s Meritorius Civilian Service
Award. This second highest award that
a civilian employee can receive is the
second one for Dr. Sommer. His first
came 24 years ago from the Depart-
ment of Commerce.
Dr. Sommer, Chief Scientist and As-
sociate Technical Director, Harry Dia-
mond Laboratories (HDL) Adelphi,
Maryland, was recognized for his out-
standing technical management leader-
ship in providing direction to a large
number of complex electronic research
and development programs. His contri- .
butions to proximity fuzing and nuclear
radiation effects has improved the
Army’s capability in many fields of
ordnance and electronics.
Dr. Sommer received all his degrees
majoring in electrical engineering from
Texas A&M University—BS in 1944,
MS in 1947 and PhD in 1950. In
addition he earned some graduate credits
from Massachusetts Institute of Tech-
nology during World War II. After
completing his academic requirements,
he did his thesis research at the Na-
tional Bureau of Standards in electrical
engineering and physics.
Dr. Sommer served as a radar officer
in the Signal Corps from 1943 to 1946.
He joined the Atomic Physics Section
of the National Bureau of Standards in
1949 and transferred to HDL (then the
Diamond Ordnance Fuze Laboratory)
in 1953. In 1957 he left HDL on a leave
of absence to join the staff of the
University of Florida as a research
professor in its Electronics Laboratory.
Dr. Sommer returned to HDL in 1958
and has subsequently served as Chief
of the Radio Systems Branch, Chief of
the Microwave Branch, and, finally,
Chief of the Systems Research Labora-
50
tory, where he planned, directed and
administered scientific programs involv-
ing more than a hundred engineers,
technicians and administrative person-
nel.
Dr. Sommer has authored numerous
technical publications, and is a mem-
ber of several professional societies
including the Philosophical Society of
Washington, the Washington Academy
of Sciences, the Institute of Electronic
and Electrical Engineers, and two pro-
fessional fraternities, Tau Beta Pi and
Sigma Xi.
A native of Geislingen, Wurttemberg,
Germany, Dr. Sommer came to this
country at an early age and attended
public schools in Dickinson, Texas. In
1946 Dr. Sommer married Ethel K.
Benoist, whom he began dating in col-
lege, although they are both from the
same town. The Sommers have six
children, Richard J., Kathryn T., John R.,
Stephen A., Michael T., and Michele
M.., and they live in Bethesda, Maryland.
NAVAL RESEARCH LABORATORY
Lendell E. Steele of the Naval Research
Laboratory (NRL) was presented with
the Navy Superior Civilian Service
Award for outstanding research ac-
complishments in special ceremonies on
December 9, 1976. Rear Admiral R. K.
Geiger, Chief of Naval Research, pre-
sented the award, second highest honor
that can be bestowed on civilian em-
ployees by the Navy, and the highest
honorary award given by the Chief of
Naval Research.
Mr. Steele, Head of the Thermostruc-
tural Materials Branch in the Engineer-
ing Materials Division, was honored for
his outstanding contributions to the
understanding of radiation damage to
metals. His personal contributions and
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
those under his research leadership re-
sulted in detailed understanding of radi-
ation damage effects and the influence of
these on the integrity of nuclear reactor
structures, the development of the pro-
cedures for reducing such effects and
criteria for producing metals resistant
to neutron damage for future reactor
structures.
The NRL scientist pioneered in the
development of design, fabrication and
surveillance criteria and standards which
have helped to assure the safety and
reliability of power reactors—of partic-
ular importance today because of the
increased use of nuclear reactors for
electric power production. Admiral Gei-
ger stressed that the work of Mr. Steele
and his co-workers over the past sixteen
years has produced a collective scien-
tific and engineering knowledge of major
import to nuclear reactor safety.
A native of North Carolina, Mr.
Steele began his career at NRL in 1951.
Prior to that he had been a chemist
at the Department of Agriculture, a
scientific aid at the Department of In-
terior, a physical science aid at the
Department of Commerce, and a labora-
tory assistant at Furman University. Mr.
Steele holds an MA in Economics from
the American University and a BS in
Chemistry from George Washington Uni-
versity. He resides at 7624 Highland
Street, Springfield, Virginia, with his
wife, Rowena, and two daughters,
Pamela and Linda. Two other daughters,
Joyce (Mrs. Brian McCartney) and
Carol (Mrs. Ismael Gonzalez) currently
reside in Ft. Worth, Texas.
OBITUARY
David G. Knapp
David G. Knapp, geophysicist, died
February 8, 1977, in Boulder, Colorado
following a short illness.
Born in Indianapolis, July 20, 1907,
he worked for the National Bureau of
Standards in Washington from 1926-28.
While attending Butler University he
worked for the Indianapolis Power and
Light Company, 1928—36. He obtained a
B. S. degree and in 1936 returned to
Washington for employment as a mathe-
matician in the Coast and Geodetic
Survey. This was the beginning of a
lifetime affiliation with the science of
geomagnetism. He was an internationally
known author of many scientific and
technical papers dealing with geomag-
netism and had represented his office
at many national and _ international
scientific assemblies. His principal in-
terests were mathematical modeling of
the earth’s magnetic field, in particular
for the polar areas and for location
of the dip poles, and the history of
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
geomagnetism. Most recently he had
been working on a new model of the
main field using multipoles. A book on
the history of geomagnetism, co-au-
thored with the late Sidney Chapman,
remains nearly completed. He was a
member of the American Geophysical
Union, Sigmi Xi-The Scientific Re-
search Society of North America, and
the Washington Academy of Sciences.
In the American Geophysical Union
he served as secretary of the section
of terrestrial magnetism and electricity
from 1945-50 and as a member of the
editorial and publication committee from
1950-58. He served on several com-
mittees of the International Association
of Geomagnetism and Aeronomy and was
currently chairman of a working group
on history. In 1971, along with other
geophysicists in the National Ocean
Survey of NOAA, he was transferred
to the Environmental Research Labor-
atories in Boulder, Colorado. In 1973,
again as part of a major transfer of
programs, he moved to the U. S.
$1
Geological Survey in Denver. He retired
December 31, 1974 but had continued
in USGS as a rehired annuitant. He
also retained a desk in the NOAA Na-
tional Geophysical and Solar-Terrestrial
Data Center, where he contributed his
expertise as an occasional ‘‘guest
worker.”’
He is survived by his wife Doris,
who resides at 4695 Osage Drive,
Boulder, Colorado 80303. He is also
survived by two sons, Barry and Allen,
and two daughters, Louise and Emily.
Barry and Louise reside in Boulder;
Allen in Washington, D. C.; and Emily
in Redwood City, California.
—K. L. Svendsen
NOAA/NGSDC
Boulder, CO 80302
NOTICE
Annual Meeting— Association of Official Analytical Chemists
91st Annual Meeting of the Association of Official Analytical
Papers and symposia on methods of analysis for materials and
products important to the environment, health, and agriculture, i.e.,
drugs, pesticides, food, beverages, food additives, cosmetics, feed,
fertilizers, microbiological contamination of foods, forensic materials,
L. G. Ensminger, Executive Secretary, AOAC, Box 540, Benjamin
Date: October 17 to 20, 1977
Where: Marriott Hotel, Twin Bridges, Washington, DC 20001
Type of
Meeting: Chemists
Theme:
environmental pollutants, and related subjects.
Contact:
Franklin Station, Washington, DC 20044
52
J. WASH. ACAD. SCI., VOL. 67, NO. 1, 1977
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VOLUME 67
) Number 2
Jour nal of the JUNE, 1977
WASHINGTON
ACADEMY., SCIENCES
Issued Quarterly
at Washington, D.C.
CONTENTS
Feature:
SIMON W. STRAUSS: L’Hopital’s Rule as a Chemist’s Tool ........
Review:
WILLIS W. WIRTH: A Review of the Pathogens and Parasites of
the Biting Midges (Diptera: Ceratopogonidae)................... 60
Research Reports:
CONRAD P. HEINS: Wheel Load Distribution on Steel Bridge
Raia; Kale Leslaiie) ene) wim lala a) eite)\'s, was el elie (e «0! \«, ‘« \«) (6 ‘aie -e .= e/: #6 |e) e: ene 6),@| a) .8))'s eye 6, 6 se
DOUGLAS H. UBELAKER: Drilled Human Teeth from the Coast
SORE PEA SA Oe ra. Neco: ee oe are ie he ot EO UIE ARS
Academy Affairs:
The Awards Program of the Academy and Recent Honorees .........
RR me RRS Nn enn a, ee Penpals, yan tec hos oak «la Pele ay ese
Obituaries 66.2 98.2: Scr ales hk kat ten eo ete ee
Washington Academy of Sciences
EXECUTIVE COMMITTEE
President
‘Richaia H. Foote
President-Elect
Mary H. Aldridge
Secretary
Kelso B. Morris
Treasurer
Alfred Weissler
Members at Large
George Abraham
Grover C. Sherlin
BOARD OF MANAGERS
All delegates of affiliated
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EDITOR
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ACADEMY OFFICE
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Founded in 1898
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DELEGATES TO THE WASHINGTON ACADEMY OF SCIENCES,
REPRESENTING THE LOCAL AFFILIATED SOCIETIES
Eimerscrilical: SOCIetYy Of WaShiINPTON (25 oie Ne ie ale eet nce a ce ereoesteveleus James F. Goff
Parnemerical Society Of WaSHinGiONn 2.23.5 oe )cie cles wee hele oe Selene owes sew eeecwcoed Jean K. Boek
Pepe te SOCIETY Of. WaASMINGION: <.. 26 .so0 cen Sis ead ew diedele s Seve Ube aul cebiacee ees William R. Heyer
tee CISL Ok WW ASHINIP LOM oc. 0 5 aos ic ke a his esa weblale Grae 6 ois dd od wae sib bidwd lee ve = David H. Freeman
Pmmmamericdl Society Of WaShiNStON 05 666.0856. Melee kc wee cence cde e eee awenees Maynard Ramsay
MEME MEE MOEA HIC SOCICIY er) is tS os A caek asc womee oabercs cles T. Dale Stewart
Pe mipmic ae SOCIeLy Of. WASHINGION «2.55 ccc ee daa ee ce ene ces cece re sauleuswsads Marian M. Schnepfe
nae temcicty Of the District of Columbia 2.05... 00s Se ce eect be ce ecw ecco cueeeusus Inactive
pena PEL ISO OIC A SOCIEOY 4c © soles foes hoses die esas 4 sacle ade ae Ue seee hse bees accace wos Paul H. Oehser
eC MESORICEYNOL VWVASMINIQUON: 656.5060. -. plays ce cercle a edie ele Peiaiele cS ocisla iow baie ogra oe beens Conrad B. Link
Se mm ATMERICAN: POFESLETS. bac «6. 5 adic oc sod ess vee se whew cen viva euneds Thomas B. Glazebrook
PaO CICLY Ol MPINCEIS) -)oisirsice ya os Keele wb mae as Gea Vek ese ideedaecaieads George Abraham
fase of Electrical and Electronics Engineers ....2.........050000csceeeececeuscs George Abraham
Pumienicam Society Of Mechanical Engineers «...6. ccc ce cee lec ce ee cede nwt ecceeenvoes Michael Chi
Hetmintholopical Society.of Washington «<.:.............cescceeccsctacccccences Robert S. Isenstein
PaMCEeam SOCIeLy 10M MICFODIOIORY ©. 2.6. eels ee ea he ee ee Se ee ec ee cess eaeee Michael Pelzcar
Pee IMeNICAT MINitATY ENPINCEIS . 2... 5c. cc ee ce cee eee ence eee eeas H. P. Demuth
Punciveanesociety Of Civil ENGINEEIS .. 2... 255.6 eee ee lee kee cee ete acenenes Robert Sorenson
Sorcwior expermental Biology and Medicine ..............0.56. 0c cece cee ee ees Donald Flick
SA SETI SATE SVGIE STO? CCTM [ot LSP IN Ne ee Glen W. Wensch
international Association of Dental Research ........6.....2.0.00ccee cee enone William V. Loebenstein
American Institute of Aeronautics and Astronautics .............. cece eee eee eee eee George J. Vila
Pe ne anen eC OLOlGeiCal SOCICLY © 2 5.<.. seis dis)oihs Scie pln old ale she We eee dla deena dee ele A. James Wagner
ec ereimeOClety Or VV ASNINGTOM |. 1-6. fe eed cela sabe kee ce seb yp eeceaees Robert J. Argauer
See SOCIOL OL AMICKIC A. Heli -16 fa dos clase edad oe ee cee a robe we We en Delegate not appointed
Ree ACT CIC ATH OOCICLY Seen tes Mine Me alee cin oe Kee ks bind a wie Y se kb Chee ee ee gaa ee Dick Duffey
tn eCTOMEOOd VECHMOIOCIS(S” 26... 1 bce l cc eic cae Ses cheese nbaeeceeneeseceta William Sulzbacher
ee th CRAM COON a re Or eteinc 2 oie rs ue ok ial aie sie Eels a a Sie o's Pakere a ieee oe oid SRN es ave Inactive
Pr IPCTILC ANS OC ICLV Te og esis) ae ee oleh fae ce ae wh he nie eo are wale bse sense Delegate not appointed
SNP CUMIN ORIOL SCIENCE CUD, es ys, c ici slave cui cre oie G58 sinie Fe.aine dh ales able 6 64-6 0's wince oo e Inactive
Pameie ane ASSOciationiof Physics, TEaCHEFS ..22 4. be sce hice sense n cee om Seles eben dees To be appointed
Ee ESPINER CTE A sete als) 2, os) eas elie ch noses Sle Fear a Riavacone) 0 ae 48) eos «platen ple dfalds Lucy B. Hagan
mimemean Society Of Plant Physiologists... :<s0).-4. ses ec ec cee ec eee se a weenie ees Walter Shropshire
asmincion Operations Research Council. ..:... 2.2 bos See kek cas a cede ewes eeeee John G. Honig
Peenye He SOCIEC VION AINEHCAW). dis. s c)o0 s Obes twee be bwla sed Deega dee oelaee Saves cewbee aces Inactive
American Institute of Mining, Metallurgical
CIRCLE MIM ENGINEERS: | Ao) ci58 os ate cele iv vies acto ee es We ds els pels e siiels ep elec bce t's Philip W. Guild
Ma MMOAGIION ASERONOMENS soe c 6c kc kb oO cstse's see c ce tcws euavseeee@dvseccecene Benson J. Simon
edema SSOCIAMON Ol AMECIICA foe. ci ce he de nec cets ey enc bens e ween ae enenccrneas Patrick Hayes
SIASTIBIME Wl CHEMISES. ae)o 8 alin cs beolew ae a cso tie Seles s aiiee ce oe eed aise se oni eee Miloslav Recheigl, Jr.
Pee BESVECHOIOPICAIVASSOCIALION 6 ....65 65.2 se wee nie ones se bad enene denise teen ee seen es John O’ Hare
Siew vashineton Paint echnical Group... 2. i os... eeciee ek cow ee cen ee cows eceeees Paul G. Campbell
Pacmean EnvtOpatnological SOGICLY® 25540 .K uses ce cee ete wee casio eee gensee ss aen Tom van der Zwet
Bucieny tov General Systems Research «2.2... oi5 22. eee cee cece nee Ronald W. Manderscheid
Rae TRIES TE LOE SS OCICUN Mes os 2 ye )es uel ete lo De adie sided We a p's ade 's oe dew a Sah Olle oa’ H. McIlvaine Parsons
Delegates continue in office until new selections are made by the representative societies.
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977 53
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FEATURE
L’Hopital’s Rule As A Chemist's Tool
Simon W. Strauss
Directorate of Science, Director of Science and Technology, HQ Air Force Systems
Command, Andrews Air Force Base, Maryland, 20334
ABSTRACT
The usefulness of L’Hopital’s rule as a practical alternative method for the
evaluation of chemically oriented indeterminate forms is illustrated with examples
chosen from chemical kinetics, solid state theory, chemical engineering, and
thermodynamics.
Physical chemistry textbooks use 2
general approaches for dealing with those
special cases where rate equations be-
come indeterminate. The one most fre-
quently used involves imposing on the
original differential equation the same
condition that made the integrated rate
equation one of indeterminate form. Inte-
gration of the modified differential equa-
tion yields the desired rate equation (see,
for example, Moore (1)). An interesting
variation of this procedure is given by
Rose (2). The second approach involves
the use of series to evaluate the indeter-
minate forms (see, for example, Glas-
stone (3)).
An alternative method to the above
(not discussed in physical chemistry
textbooks) which can be used simply
and effectively to evaluate indeterminate
rate equations as well as other indeter-
minate expressions arising in chemistry
and elsewhere, involves the application
of the so-called L’ H6pital’s (also spelled
L’H6spital’s) rule. In this connection, it
appears befitting to point out that Mellor’s
Higher Mathematics for Students of
Chemistry and Physics, the fourth edition
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
of which was published over 60 years ago,
contains a student exercise requiring the
use of L’H6pital’s rule to evaluate a
second order rate equation of indeter-
minate form (4). The purpose of the
present paper is to illustrate the useful-
ness of L’H6pital’s rule as a practical
alternative method for the evaluation of
some indeterminate forms which may be
of interest to chemists and chemical
engineers as well as to some physicists.
A number of mathematical theorems,
usually referred to collectively as
L’ Hopital’s rule (to be referred to hence-
forth as L. R.), provide an important
technique for finding the limit of a
quotient of 2 functions in circumstances
such that the limit cannot be found
directly by the rule that the limit of a
quotient is the quotient of the limits (5,6).
For the purpose of the present paper,
L. R. may be stated as follows: If the
quotient f(x)/g(x) assumes an indeter-
minate form 0/0 or ~/o when x = u,
where u may be finite or infinite, then
lim fix)
l
zu g(x) o
55
will be equal to the first of the following
expressions which is not indeterminate
provided this expression exists; and if it
fails to exist, the limit sought also fails
to exist:
_ (d/a)E FON), (2 /axL FO],
ru (d/dx)[g(x)] 2» (d?/dx*)[g(x)]
mm FL A2 LLC)
@/deMe@)]
In the above notation, f(x) and g(x) are
functions of x which tend to zero or
infinity as x tends to vu. We are now ready
to apply L. R. to some chemically
oriented indeterminate forms selected
from the areas of chemical kinetics,
solid state theory, chemical engineering,
and thermodynamics.
(2)
Second Order Rate Equation (7)
For the reaction represented by the
equation
k
— Products
A B
2 mG)
(b — x) x
the integrated form of the rate equation
may be expressed as
(ag x)
x _ kt(a—b)
ic aioe serie ’ (4)
a 1 —- aekta b)
where a and b are the initial concentra-
tions of the reactants A and B, respec-
tively, a = a/b; x is the concentration
of the products at time f; and k is the
specific rate constant. At b =a; the
Qi ek.
(b ~ c) In|
kt =
(Gap) Dt
)+ (ea) n{ e
right hand side quotient of equation (4),
designated for convenience by m/v
(m = numerator; v = denominator) be-
comes indeterminate, 0/0, and is, there-
fore, an obvious candidate for application
of L. R. We wish to find the limit of m/v as
b approach a, that is, lim bo
boa V
We proceed as follows:
dm dv
ala) ©
db db
Performing and simplifying the indicated
differentiation yields
io
b—a
2
2 2 im ae
a ba a(l + bkt)
akt
= ee 7
l ae @)
or,
x
kt = ————__,, 8
| a(a — x) .
which is the desired equation.
Third Order Rate Equation (8)
For the reaction
A + 8B
(ay ND = a)
k
+ ~C -—> Products
yt?)
(e— 2) x
the specific rate constant is given by the
equation
Cae
7
Tee
)+(@- 6 n(
ENG =a)
, (10)
where c is the initial concentration of the reactant C. When c = J, the quotient, r/w,
becomes indeterminate, 0/0. Applying L. R., gives
kt = lim
c—b
alae
56
(11)
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
(ai D)
ra fee]
yt HG. s) Dia — x)
LE Ap = 9S OS cor Iie a
x(a — b) fi In| aa
co: x) gloat
= a= pe me (13)
Let us now consider equation (13) for the
special case where b = a. The quotient,
y/z, becomes 0/0. Applying L. R. to
equation (13),
d d
kt = lim m | o/s. (14)
ba | db db
which, after differentiation, followed by
simplification in a manner such as that
discussed by Thomas (9), gives
2D x) |
iia
ba | 2b7(b — x)?
2a — 2X)
2a2(a — x)?
Equation (16), is, of course, also ob-
tainable by putting a = b=c in the
kt
(15)
(16)
original differential equation and then:
integrating it.
General Case of A Rate Equation (10)
The integrated rate equation for a re-
action of the nth order, all the initial
concentrations being the same, is
ns
kt = (17)
At n= 1, qg/s becomes 0/0. Applying
oD.
kt = im | a9 /<| (18)
n—>1| dn dn
= lim
n—1
x In(a — x)] (19)
= In| oa ie
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
(20)
By letting x = a/2 in equation (17), the
general equation for the half-life, t,,., is
qin 2@a-b) — 1] h
1/2 DE : (21)
Atn = 1,h/e becomes 0/0. Applying L. R.
dh de
(on = ig) Sea 22
= tim | / =| (22)
gD)
ol e3S
= lim patios Sie ot awe (23)
n—1 k
In2
miele (24)
k
which is also obtainable by putting
x = a/2 in equation (20).
Consecutive Reactions (11)
The simplest case arises when there are
two consecutive stages of the first order,
ViZ.5
ee Be
Ment Neh iiNe
where the initial concentration of A is No;
the concentrations of A, B and C, respec-
tively, at time ¢ are N,, N. and N3; and k,
and k, are the 2 specific rate constants. It
is also assumed that att = 0, No. = Nz = 0.
The following expressions for N,, No,
and N, may be readily derived (11):
(25)
N, = Noe **, (26)
—kit — ,7-—ket
pee ee) (27)
ky ra ky
Niki es kl ey)
N; = ———__
k, i k, (28)
57
If k, = k, (12), the quotients of equations
(27) and (28) would become indeter-
minate, 0/0. Applying L.R. to each of 2
quotients in the manner illustrated in pre-
vious examples, we get the following:
No = lim Nok,te* (29)
K2—k1
= Nok,te~* (30)
NE = lin ING ee ee || (Bi)
kok
= Nil he]. (32)
Equation (32) could also have been
readily obtained by simple algebraic
means using equations (26), (30) plus the
fact that No = N, + No + Ns.
Einstein Specific Heat Equation (13, 14)
This equation may be written as
where C, is the molar heat capacity of
a solid at constant volume, R is the gas
constant, h is Planck’s constant, v is the
frequency of vibration of a particle in the
lattice, k is Boltzmann’s constant, and T
is the Kelvin Temperature. At high tem-
peratures (or more correctly as T — ©),
the quotient becomes 0/0. Applying L. R.,
gives
which is still of the form 0/0 (as T— ©);
hence we can apply L. R. again and get
3R
C, = lim
T—0
(oS)
cosh ae
kT
58
An alternative method, using series, for
obtaining equation (35) from an ex-
ponentially equivalent form of equation
(33) is given by Mandl (15).
Example from Chemical Engineering (16)
An equation encountered in absorption,
distillation, extraction and leaching is of
the form
y= ae ce)
In gas absorption, with systems where
Henry’s law applies to the gas-liquid
equilibrium, y represents the fraction of
solute in the inlet gas that is absorbed
in a tower of n perfect plates, and x is the
ratio of solute-free liquor rate to gas rate,
divided by Henry’s law constant. When
x= 1, the quotient in equation (36)
becomes 0/0. Applying L. R.,
y = lim eae = | (37)
x1 (n + 1)x”
"7 n : 1 ay
which is the desired value for y at
x = 1 (16).
Example from Thermodynamics (17)
A polytropic process is one for which
the pressure-volume relation is given by
PV" = constant, (39)
where P is the pressure; V is the volume;
and n is a constant (17). Assuming a
perfect gas, the work, W, done by the
system is
P, \e in
rv: |
Py
n—
W= . (40)
where the subscripts 1 and 2 refer to
initial and final states. At n = 1, the
quotient in equation (40) becomes 0/0.
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
Applying L. R., we obtain, after
simplification,
P, \(n—1In) P
12 P,
m eo EEEoeeorae
W i lim n2
(41)
P,
By in| 72 42
AV, in (| (42)
P
= RTIn( = (43)
P,
since for 1 mole of an ideal gas PV = RT.
Equation (43), the well known expression
for the maximum work in an isothermal
reversible expansion of an ideal gas, may
also be readily obtained by other means
(18).
Concluding Remarks
As illustrated with a number of ex-
amples in the present paper, L. R. can
indeed be used as a chemist’s tool. Per-
haps some students reading this paper
might be sufficiently stimulated to search
for applications of L. R. to some other
indeterminate forms of interest to the
scientist and engineer in general and to
the chemist in particular. To those
students, the following words of caution
might be in order: to preclude the pos-
sibility of obtaining absurd results, we
must satisfy ourselves that we are indeed
dealing with an indeterminate form 0/0
of ~/o before applying L. R. Finally,
whereas a limit that can be obtained by
L.R. can also be evaluated by elementary
methods, the use of L. R. makes the work
in general much easier (19).
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
References Cited
(1) Moore, Walter J., ‘‘Physical Chemistry,”’
4th ed. Prentice-Hall, Inc., New Jersey, 1972,
p. 336.
(2) Rose, J., ‘‘Dynamic Physical Chemistry.”’
John Wiley & Sons, Inc., New York, 1961,
p. 731.
(3) Glasstone, Samuel, ‘‘Text-Book of Physical
Chemistry,’ Ist ed. D. Van Nostrand, Co.,
Inc., New York, 1940, p. 1035.
(4) Mellor, J. W., ‘‘Higher Mathematics for
Students of Chemistry and Physics,’’ 4th ed.
Longmans, Green and Company, New York,
1912 (reprinted by Dover Publications, New
York, 1946, p. 307).
(5) Sherwood, G. F. E., and Taylor, Angus E.,
‘“‘Calculus,”’ 3rd ed. Prentice Hall, Inc., New
Jersey, 1954, p. 177.
(6) Crowell, Richard H., and Slesnick, William E.,
‘Calculus With Analytic Geometry,’ 3rd ed.
W. W. Norton & Co., Inc., New York (1968),
fo, 4,
(7) Moelwyn-Hughes, E. A., ‘‘Physical Chemistry,”
Ist ed. Pergamon Press, New York, 1957,
p. 1088.
(8) Ibid., p. 1089.
(9) Thomas, George B., Jr., ‘‘Calculus and
Analytic Geometry,’’ 3rd ed. Addison-Wesley
Publishing Co., Massachusetts, 1960, p. 42.
(10) Moelwyn-Hughes, op. cit., p. 1090.
(11) Ibid., p. 1098.
(12) Kelly, F. H. C., ‘‘Practical Mathematics for
Chemists.’ Butterworth & Co., (publishers)
Ltd., London, 1963, p. 101.
(13) Rose, J., op. cit., p. 1095.
(14) Dence, Joseph B., *‘Mathematical Techniques
in Chemistry.”’ John Wiley & Sons, New
York, 11975;/p.. 52.
(15) Mandl, F., ‘‘Statistical Physics.’’ John Wiley
& Sons, Ltd., London, 1971, p. 155.
(16) Sherwood, Thomas K., and Reed, Charles E.,
‘‘Applied Mathematics in Chemical Engineer-
ing,’ Ist ed. McGraw-Hill Book Co., Inc.,
New York, 1939, p. 21.
(17) Keenan, Joseph H., ‘‘Thermodynamics.”’
John Wiley & Sons, Inc., 1941, p. 103.
(18) Rose, J., op. cit., p. 34.
(19) Ginzburg, A., ‘Calculus,’ (Problems and
Solutions). Holden-Day Inc., San Francisco,
1963, vol. 1, p. 66.
59
REVIEW
A Review of the Pathogens and Parasites
of the Biting Midges (Diptera: Ceratopogonidae)
Willis W. Wirth
Systematic Entomology Laboratory, IIBIIT, Agr. Res. Serv., USDA,
clo U. S. National Museum, Washington, D. C. 20560
ABSTRACT
A review is presented of all published information on parasites and pathogens of
biting midges of the dipterous family Ceratopogonidae. Viruses furnished two records;
Rickettsiae 1; Bacteria 6; Fungi 8; Protozoa 23; Nematoda 21; Acarina 18; and Insecta
Hymenoptera 4. A bibliography of 90 titles is given. It is believed that mermithid
nematode parasites offer some promise in biological control of Culicoides disease vectors.
The literature on natural enemies of
biting midges is not extensive. Helpful
reviews were published by Weiser (1963a,
1975), Jenkins (1964), and Bacon (1970).
This review has been prompted by my
involvement in 3 related review projects:
1) a compilation of a complete bibliog-
raphy and a key-word in-context index
to the published literature on the Cerato-
pogonidae (Atchley, Wirth, and Gaskins,
1975); 2) preparation of introductory
chapters on ceratopogonid biology for
a manual to the genera of the Ceratopo-
gonidae (Wirth, Ratanaworabhan, and
Blanton, in preparation); and 3) prepara-
tion of a chapter on parasites and
pathogens of biting midges for a revision
of Jenkins’ World Health Organization
bulletin (1964). In each of these activities
different emphasis has been placed on
content and organization of the informa-
tion to be included, depending on the
primary purpose of the review. I am here
choosing a format to bring to the attention
of workers interested in the control of
biting midges a resumé of the known
60
pathogens and parasites offering the most
promise in biological control.
For brevity a decision was made,
perhaps too arbitrarily, to exclude, or to
mention only briefly, references to several
groups of parasites of ceratopogonids
that probably would have little signif-
icance in biological control. These in-
clude protozoan and nematode parasites
pathogenic to birds and mammals for
which ceratopogonids are known to be
alternate hosts without suffering known
adverse effects from the parasitism.
Examples are bluetongue virus and the
filarial parasites just mentioned, and
Haemoproteus, Hepatocystis, and Leu-
cocytozoon protozoans. Some of these
organisms have considerable medical or
veterinary literature concerned with dis-
ease transmission in vertebrate hosts.
A discussion of predators of Cerato-
pogonidae would be too long and involved
to include here and should be the subject
of a separate review. The prey habits of
predators tend to be less specific, and
preliminary studies of predation tend to
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
include more fortuitous records than
studies of parasites and pathogens. Our
interest and knowledge of the possibilities
_ of biological control of biting midges are
still in such an early stage that a mean-
ingful review cannot be made. Yaseen
(1974) searched for natural enemies of
West Indian ceratopogonids for nearly a
year without finding any parasites or
pathogens. The only natural enemies
found were adults of a tiger-beetle,
Cicindela suturalis F., which fed on
pupae and adults of Culicoides phle-
botomus (Williston).
Insect resistance to pesticides and
environmental concerns about long-range
effects of repeated applications of pesti-
cides have led to emphasis on alternative
methods of control. Integrated control,
which calls for the timely and frugal
application of pesticides while exploiting
every possibility for the use of natural
enemies and habitat management, offers
the maximum promise for relief from
damage and annoyance caused by insect
problems. A detailed knowledge of the
ecology of insect pests and their natural
enemies is essential for effective control.
Compared with mosquitoes, lice, fleas,
and some other bloodsucking pests of
man and domestic animals, research on
the biology and natural enemies of biting
midges (Ceratopogonidae) has received
little emphasis. Because of their small
size and difficulty of colonization com-
paratively little work has been done in
determining ceratopogonid vectors of
disease organisms of medical and vet-
erinary importance. Lacking a proven
basis as disease vectors, the study of
ceratopogonids has been further neg-
lected. Our knowledge of natural enemies
_ of biting midges is in an early embryonic
stage, compared with what is known, for
instance, for mosquitoes.
Viruses
Chapman et al. (1968) and Chapman
(1973) reported the first pathogenic virus
in a biting midge. Over an 11-month
period in Louisiana they found nearly
50% of the larvae of Culicoides arboricola
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
Root and Hoffman from 3 tree holes
infected with an iridescent virus (CulV).
Infection caused death of the larvae.
Infected dead larvae placed in several
other tree holes eventually produced some
infected Culicoides larvae.
Clark and O’Grady (1975) collected
larvae of Culicoides cavaticus Wirth and
Jones from tree holes in California that
exhibited symptoms of a disease similar
to that caused by the ‘‘tetragonal virus’’
reported by Kellen et al. (1963), Clark
and Chapman (1969), and Stoltz et al.
(1974) in mosquitoes in California and
Louisiana. ‘‘Infected larvae were easily
identified by their sluggish activity, which
contrasted sharply with their normally
rapid swimming movements. As the
disease progressed, the body of the larva
stiffened, first in the middle segments and
then toward both extremities. Heart
pulsations could be detected after the
extremities ceased movement. After
death, the body remained rigid and
straight until post-mortem changes re-
sulted in the dissolution of larval tissues
. In the original collection, all of the
Culicoides larvae eventually died with
the symptoms just described. In subse-
quent collections, the mortality rate
ranged from about 70 to 90%’’. Non-
occluded viruslike particles from various
tissues of the larvae were observed with
the aid of an electron microscope.
Apparently normal larvae usually died
about 3 days after exposure to water
contaminated with the remains of larvae
killed by the disease. Attempts to infect
Culex and Aedes mosquito larvae and
Musca domestica larvae by feeding them
infected Culicoides tissues were negative.
Rickettsiae
Hertig and Wolbach (1924) found tiny,
rickettsia-like cocci, diplococci, and
short rods in smears of the bodies of
adults of Culicoides sanguisuga (Co-
quillett) from Massachusetts. Nine out
of 27 individuals were infected, the
rickettsiae occurring free in smears of the
abdomen, although greater numbers were
seen in lobes of the fat body.
61
Fig. 1. Mycetome of bacteria in thorax and anterior abdominal segments of Dasyhelea imago (after
Buchner, 1930). Fig. 2. Stages in budding cells and spore formation of the fungus Monosporella
unicuspidata in Dasyhelea obscura (after Keilin, 1920); a, ascus; sp, ascospore. Fig. 3. Different aspects
of the diaspores of Carouxella scalaris in Dasyhelea lithotelmatica after their liberation, showing the
stout protoconidia and slender conidia (after Manier et al., 1961). Fig. 4. Adherent mycelium of
Rubettella inopinata in Dasyhelea lithotelmatica (after Manier et al., 1961).
62 J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
Bacteria
Keilin (1921a, 1927) found 2 pairs of
masses of bacteria present in the body
cavity of the thorax of Dasyhelea
obscura (Winnertz) in England. These
organisms, which he termed “‘hereditary
bacterian symbionts,’’ pass from stage to
stage in these masses and appear in the
egg stage. Stammer (in Buchner, 1930)
reported similar bacteria forming a
syncytium in mycetomes in the thorax
of Dasyhelea versicolor (Winnertz) in
Germany (fig. 1). Mayer (1934) observed
similar mycetomes in larvae of Cu-
licoides species in Germany. Lawson
(1951) found bi-refringent, non-fluo-
rescent, minute, motile particles in cells
of the fat bodies of Culicoides nubeculosus
(Meigen) in Britain, that he speculated
may be symbionts of the type found by
Keilin. Becker (1958) identified as Pseu-
domonas sp. fluorescent bacteria isolated
from larvae of Culicoides salinarius
Kieffer in Scotland. He presumed that
these bacteria were also symbiotic.
Fungi
Keilin (1920a, 1921a, 1927) described
an Ascomycete fungus, Monosporella
unicuspidata, from the body cavity of
larvae of Dasyhelea obscura (Winnertz)
in England (fig. 2). Infected larvae could
be recognized by their milky appearance.
The fungus is pathogenic to the larvae,
which die with the body cavity com-
pletely filled with the spores of the
fungus.
Ciferri (1929) grew cultures of Gruby-
ella ochoterenai, a fungus parasite orig-
inally collected in Mexico from dead
bodies of Simulium larvae, in the lab-
oratory in the Dominican Republic on
adults of Culicoides phlebotomus (Wil-
liston). Mayer (1934) reported finding
Ascomycete fungi of the group Laboul-
beniales on Forcipomyia sp. in Germany.
According to Steinhaus (1949) these fungi
are usually harmless commensals.
Manier et al. (1961) described 2 new
Trichomycete fungi from Dasyhelea
lithotelmatica Strenzke in France: Rube-
tella inopinata (fig. 4) and Carouxella
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
scalaris (fig. 3). The first develops in the
anterior part of the hind gut and the
second in the rectal ampullae of the
Dasyhelea larvae. Gol’berg (1969) re-
ported an epizootic among ceratopogonid
midges in a water reservoir in the filtra-
tion fields of a village near Moscow
caused by Entomophthora_ ovispora
Nowak.
Megahed (1956) found ‘‘fungal hyphae’”’
in the lumen of the oesophageal diverti-
culum of Culicoides nubeculosus
(Meigen) in laboratory colonies in Britain
and speculated that the spores must have
been ingested with raisin sap and have
developed within the diverticulum. Lewis
(1958) found fungal hyphae in the duct of
the crop of a dissected female of Culi-
coides furens (Poey) in Jamaica.
Protozoa
Weiser (1963a) stated that while mem-
bers of every protozoan class parasitize
insects, the important pathogens belong
to the Gregarina, Coccidia, Microspor-
idia, and Haplosporidia. Most species
found in the intestinal tract are harmless
commensals, whereas those living in the
gut walls may cause tissue destruction
and death of the host.
Ciliata
Ghosh (1925) described a ciliate,
Balantidium knowlesii (fig. 5), from the
coelomic cavity of Culicoides peregrinus
Kieffer (stage not given) in India.
According to Jenkins (1964) this species
is a synonym of Tetrahymena pyriformis
(Ehrenberg). Laird (1960) stated that
Tetrahymena ciliates are normally free-
living but may invade wounded or
moribund larvae of mosquitoes, and
sometimes even healthy ones. In 1959
Laird reported that T. pyriformis is a
well-known facultative parasite of vari-
ous mosquitoes and other aquatic insects.
Chapman et al. (1969) reported a ciliate
identified as Tetrahymena sp. from
larvae of Culicoides probably nanus
Root and Hoffman in Louisiana. Sharp
(1928) reported unidentified ciliates from
the dissected bodies of 3 out of 540
63
Fig. 5. Balantidium knowlesii from the coelomic cavity of Culicoides peregrinus (after Ghosh, 1925).
Fig. 6. Taeniocystis parva, a gregarine from the larva of Forcipomyia sp. (after Foerster, 1938). Fig. 7.
Stylocystis riouxi, an eugregarine parasite from the larva of Dasyhelea lithotelmatica (after Tuzet and
Ormiéres, 1964). Fig. 8. Life cycle of Helicosporidium parasiticum from Dasyhelea obscura; a,
schizogonic multiplication; b, formation of morula; c, spore formation; d, stages in opening of
sporocyst, unrolling of spiral filament, and liberation of sporozoite (after Keilin, 1921).
64 J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
a
mT oe |
wild-caught females of Culicoides austeni
Carter, Ingram, and Macfie in the
Cameroons.
Becker (1958) reported ciliates iden-
tified as Perezella sp. (Perezellidae,
Astomata) living in the haemocoeles of
Culicoides larvae in Scotland. Up to 20%
of the larvae in various samples were
parasitized, and the number of parasites
per larva varied from a few until they
became closely packed in the haemocoel.
Culicoides salinarius Kieffer, odibilis
Austen, and riethi Kieffer were para-
sitized. Becker quoted unpublished ob-
servations of Kettle in Scotland of these
parasites in a larva of C. pulicaris (L.),
and of ectoparasitic cysts, presumably
also of Perezella, occurring frequently
near Glasgow on larvae of C. cubitalis
Edwards and pallidicornis Kieffer. Kettle
and Lawson (1952, plate 17a) illustrated
these ‘‘ectoparasites’’ on the head and
neck of a C. pallidicornis larva.
Mastigophora
Weiser (1963a) believes that gut flagel-
lates found in the intestinal tract of
insects are harmless commensals. Sharp
(1928) reported, for example, that flagel-
lates of the leptomonas type were seen
on a number of occasions in dissections
of females of Culicoides austeni Carter,
Ingram, and Macfie in the Cameroons.
Kremer et al. (1961) observed that a
large proportion of the larvae of Cu-
licoides salinarius Kieffer had in their
digestive tube a smal! flagellate similar
to but smaller than the Strigomonas
found in Culex.
Recently Hommel and Croft (1975)
discovered a flagellate which they placed
in the genus Herpetomonas Kent infect-
me 2 to 5% of the adults in the
laboratory colony of Culicoides varii-
pennis (Coquillett) at Pirbright, England.
The parasites were always localized in
the Malpighian tubules and sometimes in
the midgut and hindgut of the adult
midges, and occurred in either opistho-
mastigote or promastigote stages with a
long flagellum. In culture on 4N medium
the parasites transformed into aflagellar
multiplicative stages with a high degree
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
of polymorphism. The forms with long
flagella reappeared in culture after 6 to
8 days. The life cycle was not worked
out, but the authors believed that probably
early stage midge larvae were infected
by forms released by the adult midges.
This was the first record of a Herpeto-
monas in the family Ceratopogonidae.
Gregarinida
According to Weiser (1963b) the greg-
arines parasitic in insects fall in two
main classes: (1) Eugregarina, most of
which are harmless gut-inhabiting com-
mensals, rarely invading the epithelial
tissues, and have lost the schizogonous
part of their life cycle. (2) Neogregarina
(or Schizogregarina) which invade and
undergo schizogony in the gut wall or
other tissues and often cause death or
serious harm to their host. Tuzet and
Rioux (1965) reviewed the classifica-
tion and life cycles of the gregarines
of Ceratopogonidae and other biting
Nematocera including the species dis-
cussed below.
Schizocystis gregarinoides Léger (1900)
is a neogregarine parasite in the gut
wall of Ceratopogon sp. (Léger, 1900)
and Bezzia solstitialis (Winnertz) (Léger,
1906) in Europe, parasitizing up to 50%
of the larvae sampled and causing the
death of the host during metamorphosis.
On the other hand the eugregarine
Taeniocystis mira which Léger (1906)
described from B. solstitialis in France
is less common, infecting up to 20% of
the larvae observed, with only 1 to 4
parasites in each larva, and causing little
pathological damage to its host. Foerster
(1938) described a second TJaeniocystis
species, 7. parva (fig. 6), from larvae of
Forcipomyia sp. in Germany.
Keilin (1920b, 1927) described an
eugregarine, Allantocystis dasyhelei, from
larvae of Dasyhelea obscura (Winnertz),
which lives in decomposed sap in wounds
of trees in England. These parasites
were rare, and the hosts were never
heavily infected; all stages of the greg-
arine live in the midgut of the insect
larva between the intestinal epithelium
and the peritrophic tube. A fourth
65
eugregarine ceratopogonid parasite, Sty-
locystis riouxi (fig. 7), was described by
Tuzet and Ormiéres (1964) from larvae
of Dasyhelea lithotelmatica Strenzke
in France.
Microsporidia
According to Weiser (1963a) the Micro-
sporidia are the commonest parasites of
medically important insects. Infected
hosts are not easily detected unless their
bodies are transparent enough to dis-
tinguish the opaque-white tissues packed
with masses of spores. Microsporidia are
pathogenic to some insects while having
little pathogenicity to others, having
reached a suitable equilibrium with their
host.
Léger and Hesse (1922) described 2
microsporidians from the fat bodies of the
larvae of Ceratopogon sp. in France:
Spironema octospora and Toxonema
vibrio. According to Jirovec (1937) and
Weiser (1963b) the correct names for
these parasites are now Spiroglugea
octospora (Léger and Hesse) and Tox-
oglugea vibrio (Léger and Hesse). Keilin
(1927) also mentioned a parasite which
he stated was probably a Glugea sp.,
invading the fat body and salivary glands
of Dasyhelea larvae in England.
Weiser (1957, 1961, 1963b) described
Nosema sphaeromiadis from a larva of
Sphaeromias sp. in Czechoslovakia. The
parasites were found in the fat body
of the larva. Chapman et al. (1967, 1968,
1969) reported 2 species of Plistophora
(also nosematids) from at least 2 species
of Culicoides in Louisiana. One species
was observed in Culicoides larvae from a
shaded woodland pool. A second species
in larvae of Culicoides nanus Root and
Hoffman from tree holes caused death
just before pupation. In 1969 Plistophora
sp. was found in Culicoides arboricola
Root and Hoffman. Chapman (1973)
later reported another parasite of C.
nanus, an unnamed new species of
Nosema, from another tree hole at his
laboratory. He stated that the levels of
infection in these field populations were
always less than 1% and that attempts
66
to transmit these parasites to mosquitoes
were unsuccessful.
Helicosporidia
Some workers consider this group is
closely related to the Microsporidia,
but with a peculiar sporogony in which
the sporoblast (fig. 8) divides into 4
cells included in a spherical spore. Three
of these cells develop into sporozoites,
but the fourth changes into a long
nucleated filament which apparently
functions in opening the spore like an
uncoiling spring. The only named species
is Helicosporidium parasiticum Keilin
(1921a), described from larvae of Dasy-
helea obscura (Winnertz) in England.
Later this parasite was reported from a
wide range of insect hosts in Europe
and North and South America (Weiser,
1970; Kellen and Lindegren, 1973).
Weiser considered Helicosporidium more
likely to be a primitive Ascomycete
fungus related to the Nematosporoideae
of the Saccharomycetaeae, but Lindegren
and Hoffman (1976) suggested that the
spore structure showed more affinity with
the Protozoa than with the Ascomycete
fungi. Most recently Fukuda et al. (1976)
were of the opinion that the Helico-
sporidium infecting beetles and mos-
quitoes were 2 distinct species differing
from H. parasiticum. They indicated
that these parasites showed considerable
promise as biological control agents
against mosquitoes, but that this is
dependent upon further testing for safety
to mammals and other non-target or-
ganisms.
Haemosporidia
Several Haemosporidia are found in
ceratopogonid adults but will only be
mentioned briefly here because of their
minor pathogenicity to the insect hosts.
Their primary interest as parasites con-
cerns their pathogenicity to their verte-
brate hosts. Fallis and Bennett (1961)
and Bennett et al. (1965) have reviewed
this group, which includes such genera
as Parahaemoproteus which undergoes
part of its life cycle in various birds and
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
—_—— Be ee ee
part in Culicoides midges; Akiba caulleryi
(Mathis and Léger), a pathogenic par-
asite of poultry in Japan transmitted by
Culicoides arakawai (Arakawa); and
Hepatocystis kochi (Laveran), a malaria
parasite of Cercopithecus monkeys in
Kenya transmitted by Culicoides adersi
Ingram and Macfie.
Nematodes
The nematode parasites of biting
midges offering the most promise in
biological control belong in the super-
family Mermithoidea, family Mermithidae
(Nickle, 1972, 1973). However, mention
should be made of several filarial par-
asites of vertebrates that use Cerato-
pogonidae as their alternate hosts.
Filarioidea
Many important mosquito-borne filarial
parasites of man and domestic animals
are well known, for example Wuchereria
bancrofti (Cobbold) causing elephanti-
asis in man over much of the tropics, and
Dirofilaria immitis (Leidy) causing heat-
worm of dogs and cats. Onchocerca
volvulus (Leuckart), causing blindness
in man in Africa and Central America,
is transmitted by Simuliidae. It has been
shown that Dirofilaria infections may
produce heavy mortalities in Aedes
aegypti (Linnaeus) vectors and _ that
Simulium mortality increases with heavy
infections of O. volvulus. It could also
be expected that ceratopogonids, being
much smaller insects than mosquitoes or
blackflies, would suffer heavy mortality
from filarial parasitism. Schacher (1973)
gave a comprehensive review of filarial
life-cycle patterns and a synopsis of life
cycles including insect vectors.
Acanthocheilonema perstans Manson,
a non-pathogenic parasite of man in
Africa, is transmitted by several Cu-
licoides species, notably C. austeni
Carter, Ingram, and Macfie, and C. inor-
natipennis Carter, Ingram, and Macfie
(Sharp, 1928; Hopkins and Nicholas,
1952; Duke, 1954, 1956). Another human
filaria in Africa, Dipetalonema strepto-
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
cerca Macfie and Corson, is transmitted
by Culicoides grahamii Austen (Henrard
and Peel, 1949; Duke, 1954). A non-
pathogenic human filaria, Mansonella
ozzardi Manson, was found to be
transmitted by Culicoides furens (Poey)
by Buckley (1934) in the West Indies,
and Romana and Wygodzinsky (1950)
infected C. paraensis (Goeldi) with this
parasite in Argentina.
Filarias of the genus Onchocerca are
transmitted by Culicoides species as well
as by blackflies. Steward (1933) infected
C. obsoletus (Meigen) and C. nubecu-
losus (Meigen) with Onchocerca reticu-
lata Diesing, the filaria that causes
fistulous withers in horses in Europe and
North America.
Bergner and Jachowski (1968) traced
the development of Macacanema for-
mosana Schad and Anderson, a filarial
parasite of Taiwan monkeys, in Cu-
licoides amamiensis Tokunaga in Taiwan.
Robinson (1961) reported early develop-
ment of microfilaria in Culicoides crepus-
cularis Malloch that had fed on an
infected starling, and in 1971 found that
C. crepuscularis was the vector of
Chandlerella quiscali (von Linstow),
a filarial parasite of grackles. Forcipomyia
(Lasiohelea) velox (Winnertz) was found
by Desportes (1941, 1942) to transmit
a filarial worm Icosiella neglecta Diesing,
in frogs in France.
Mermithoidea
According to reviews by Welch (1963),
Bacon (1970), and Nickle (1972, 1973)
most of the mermithoid parasites of
Ceratopogonidae fall in the family Mer-
mithidae. In this family only the larval
stages of the worm are found in the body
of the insect host. In a typical life
cycle of Mermithidae the second stage
juvenile nematode, armed with an odonto-
‘style, penetrates the host cuticle and
enters the haemocoel. The mermithid
feeds on the haemolymph, grows, molts
through a number of larval stages, and
when approaching maturity, exits through
the host cuticle. Mermithids usually
select an early instar larva to parasitize;
67
those that parasitize aquatic insects may
be host specific or have a wide range of
related host species.
There are 2 types of life cycles in
aquatic mermithids. In the first, illustrated
by the mosquito parasite, Romano-
mermis culicivorax Ross and Smith, the
mermithid eggs are laid in the bottom
of a mosquito pool. After hatching the
mermithid larva penetrates an early instar
mosquito larva, often migrating to the
thorax, grows quickly, and emerges from
the fourth instar mosquito larva which
is killed before pupation. Within 2 or 3
weeks the nematode molts, mates, and
lays up to 3000 eggs in the bottom of the
pool. This type of mermithid life cycle
offers great promise in biological control,
and the laboratory culture and release of
mermithid eggs is now being undertaken
on a large scale over the world. The
Romanomermis parasite of Culicoides
nanus Root and Hoffman reported by
Chapman et al. (1968) and Chapman
(1973) has this type of life cycle (Chap-
man, pers. com.).
In the second type of life cycle,
illustrated by Perutilimermis culicis (Stiles)
from the saltmarsh mosquito, the mermi-
thid eggs are also laid in the bottom of
a mosquito pool. The mermithid larva
hatches and enters an early instar
mosquito larva, remaining in the head of
thorax and not growing at this time. When
the mosquito pupates, the mermithid
moves to the abdomen but does not
enlarge until the mosquito reaches the
adult stage and after it has had a blood
meal. The mermithid grows rapidly and
sterilizes the mosquito, then leaves the
host, killing it in the process, while still
a larva. The mermithid then enters the
pond, molts, mates, and lays thousands
of eggs to complete the cycle. Probably
most mermithid parasites of aquatic
ceratopogonids will have this type of life
cycle, although none has yet been worked
out in biting midges.
Most of the records of mermithid
parasitism in ceratopogonids have to
do with the formation of intersexes. In
chironomids, which have been investi-
gated in detail, Wulker (1961) found that
68
both sexes were equally parasitized by
mermithids and that intersexes had the
same cytological sex chromosomes as the
sex indicated by their external genitalia.
The physiological nature of intersex
formation remains poorly understood and
urgently needs investigation. Apparently
parasite damage to the hormonal system
is the most important factor in intersex
formation, and anatomic damage and
metabolic disturbance are secondary.
In the family Tetradonematidae the
adult stages of the worm are also found
in the body cavity of the insect host
(figs. 9-13). In Aproctonema chapmani
Nickle (1969), described from Culicoides
arboricola Root and Hoffman from
Louisiana, the nematode passes through
its larval stages in the host larvae, which
breed in water-filled tree holes. Late
instar Culicoides larvae may have 1 or
more male and female adult worms nearly
filling their body cavity. After mating
the male nematode dies, and the female,
filled with eggs, exits from the midge
larva, causing its death. The nematode
eggs are laid in the tree hole, and after
hatching the infective nematode larvae
parasitize other sand fly larvae.
Rubzov (1971, 1972) described a very
unusual mermithid from larvae of Cu-
licoides nubeculosus (Meigen) and C.
stigma (Meigen) in Siberian U.S.S.R. as
Heleidomermis vivipara. Apparently after
the adults mate the eggs of this parasite
develop within the female worm which
remains within the host larva, and the
hatched mermithid larvae escape directly
from the dead Culicoides into the
habitat. Further comment on the life
cycle must await translation of the
original reports in Russian. Additional
study of this mermithid is very badly
needed to determine its potential useful-
ness in biological control of Culicoides
variipennis (Coquillett), the vector of the
virus bluetongue disease of sheep and
cattle in North America. These Culicoides
are all closely related, falling within
the subgenus Monoculicoides, and C.
variipennis is likely to be susceptible to
infection with this nematode. Chemical
control of C. variipennis associated with
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
Figs. 9-13. Aproctonema chapmani from Culicoides arboricola: 9, parasitized Culicoides larva
containing a large female and small male nematode; 10, female nematode, anterior end; 11, male
nematode; 12, female nematode, vulval area; 13, female nematode, posterior end (from Nickle, 1969).
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977 69
livestock has been impossible because
the larvae usually breed in water-filled
hoofprints and the margins of ponds or
watering places contaminated with feces
of the animals. Because the animals use
this water for drinking, larvicides pose
a toxicity problem, and some form of
management or biological control is
urgently needed. Control of the disease
is presently based on expensive and
inconvenient immunization measures.
In 1974 Rubzov described 4 additional
new mermithid species from cerato-
pogonid larvae in the USSR: Agamo-
mermis gluchovae, Gastromermis bezzii,
Spiculimermis mirzajevae, and Heleido-
mermis ovipara. In contrast to dH.
vivipara, the female worm of H. ovipara,
which develops in older instars of the
Culicoides host larvae, is oviparous. In
some populations 60% of the host larvae
are infected with H. ovipara.
Except for the species mentioned
above, very few mermithid parasites of
ceratopogonids have been identified to
genus, to say nothing of species. It should
be noted that Agamomermis is an eclectic
genus serving as a repository for species
described from immature stages, since
the generic classification is dependent
on characters of the adult worm. Rubzov
(1967) described Agamomermis heleis
from an adult Culicoides pulicaris (L.) in
the Kazakhstan SSR. Callot (1959)
described an intersex adult of Culicoides
albicans (Winnertz) in France caused by
parasitism by an Agamomermis sp. Sen
and Das Gupta (1964) reported an inter-
sex of Culicoides alatus Sen and Das
Gupta in India caused by Mermis sp., and
Das Gupta (1964) reported a Mermis sp.
causing an intersex in Atrichopogon sp.
Parasitism of ceratopogonid adults by
undetermined mermithids has been re-
ported also by Kieffer (1914) in Forci-
pomyia, by Keilin (1921a) in Dasyhelea,
by Whitsel (1965) and Glukhova (1967)
in Leptoconops, and by Buckley (1938),
Beck (1958), Smith (1966), Smith and
Perry (1967), Glukhova (1967), Chapman
et al. (1968), Boorman and Goddard
(1970), Mirzaeva (1971), and Service
(1974) in Culicoides.
70
Acarina
In view of their conspicuous pink or
reddish color and their common occur-
rence on adult ceratopogonids, it is
surprising that so few published records
exist of the association of mites with
biting midges.
Trombidiiformes
Becker (1958) reported larval trombi-
diid mites, which were described by
Vercammen-Grandjean (1957) as Evan-
siella culicoides, parasitizing adults of 4
species of Culicoides in Scotland. He also
found larvae of another species identified
as Allothrombium on the abdomen of a
female Culicoides heliophilus Edwards.
According to Vercammen-Grandjean and
Feider (1973), Evansiella Vercammen-
Grandjean is a synonym of Centro-
trombidium Kramer and the correct name
of the Culicoides parasite is Centro-
trombidium culicoides (V.-G.). Vercam-
men-Grandjean and Cochrane (1974)
described 3 new species of trombidiiform
mites parasitizing adults of 10 Culicoides
species in New York: Atractothrombium
dictyostracum, Centrotrombidium dicho-
tomicoxala, and Feiderium culicoidium.
Whitsel and Schoeppner (1967) reported
another trombidiid mite belonging to the
genus Valgothrombium parasitizing a
male of Dasyhelea mutabilis (Coquillett)
in California, and quoted another report
of this genus on a species of Culicoides.
These authors quote correspondence
with I. M. Newell to the effect that the
mites frequent moist situations where
they crawl over the substrate in search
of prey. Presumably the mites locate the
ceratopogonid pupae and attach them-
selves to the adult as soon as it emerges
from the pupa. Mites have also been
recorded parasitizing 4 species of ‘‘Cer-
atopogon’’ in the Sunda Islands by Salm
(1914), Culicoides austeni Carter, Ingram
and Macfie in Africa by Sharp (1928), a
species of Dasyhelea in Argentina by
Cavalieri (1968), and Leptoconops kerteszi
Kieffer in California by Foulk (1969).
In her account of the biology of
Forcipomyia inornatipennis (Austen) in
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
Ghana, Kaufmann (1974) described at-
tacks by mites on pupae of the cerato-
pogonid. She stated, ‘“The ever-present
_ red mites do not normally attack moving
prey but do so when movement ceases.”’
Pupae attacked by mites frequently
twisted themselves out of their larval
exuviae fastened to the substrate and in
so doing lost their fastening, and the
adults were unable to emerge.
Parasitiformes
Grogan and Navai (1975) reported
adult mites of the genus Amblyseius
(family Phytoseiidae) attached to females
of Culicoides schultzei (Enderlein) from
Nepal. Grogan (1977) recorded a second
adult parasitiform mite, Macrocheles
insignitus Berlese (family Macrochelidae)
parasitizing an adult female of Nilobezzia
schwarzii (Coquillett) in Maryland.
Hydracarina
Smith and Oliver (1976) reviewed the
parasitic associations of water mites with
imaginal aquatic insects, and summarized
the known records of Hydracarina from
ceratopogonids. The typical life history
pattern is as follows: The adult female
mite deposits her eggs on the substrate in
the aquatic habitat. Within several days
the active hexapod larva hatches and
seeks a suitable insect host on the surface
film, in the water, or on the substrate.
In any case the mite larva attaches to the
adult insect at the water surface or when
it emerges from the pupa at ecdysis. The
mite engorges on haemolymph from the
host and remains attached until the host
returns to the water. With short-lived
dipterous hosts, the engorged mite larva
then detaches from the host, re-enters the
water and seeks a place to attach its
chelicerae, form a nymphochrysalis, and
emerge as an active octopod nymph
closely resembling the adult mite. After a
variable period of maturation the nymph
attaches its chelicerae to the substrate,
forms an imagochrysalis and transforms
to a sexually mature adult. After mating
the male mites soon die but the females
go on to oviposition, completing the cycle.
Munchberg (1934) reported HAHydro-
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
droma descipiens (Miller) parasitizing
Mallochohelea inermis (Kieffer), appar-
ently the first record of a water mite
on ceratopogonids. Grogan and Navai
(1975) reported larval aquatic mites of
the genus Tyrellia (family Limnesiidae)
parasitizing species of Atrichopogon,
Bezzia, Culicoides, and Dasyhelea in
Maryland. Smith and Oliver (1976)
reported larvae of limnesiid mites, prob-
ably of a species of Tyrellia, parasitizing
Dasyhelea in Canada. The same authors
reported larval mites of the genus
Arrenurus (family Arrenuridae) on adults
of Bezzia and Sphaeromias in Canada.
Insects
Only 4 species of insects parasitic
on ceratopogonids have been recorded,
all in 2 closely related families of
parasitic Hymenoptera, and all parasitic
on the immature stages of the terrestrial
and semi-aquatic genus Forcipomyia:
Family Diapriidae: Entomacis longii
(Ashmead) on F. wheeleri (Long) in
Texas (Long, 1902), and E. californica
(Ashmead) on Forcipomyia sp. in Wash-
ington (Bedard, 1938).
Family Encyrtidae: Forcipestricis
gazeaui Burks on F. picea (Winnertz)
in Maryland (Burks, 1968; Wirth, 1975),
and F. portoricensis Gordh on F.
fuliginosa (Meigen) in Puerto Rico (Gordh,
1975). Apparently these parasites de-
velop in the larvae of Forcipomyia and
emerge from the larva or pupa, killing
the host.
Acknowledgments
I am greatly indebted to the following individuals
for advice and criticism of my manuscript con-
cerning their special fields of interest: H. C.
Chapman, U. S. Department of Agriculture, Lake
Charles, Louisiana; W. R. Nickle, U. S. Depart-
ment of Agriculture, Beltsville, Maryland; and
P. H. Vercammen-Grandjean, San Francisco, Cal-
ifornia. Linda Heath assisted with the illustrations.
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75
RESEARCH REPORTS
Wheel Load Distribution on Steel Bridge Planks
Conrad P. Heins
Professor of Civil Engineering, University of Maryland, College Park, MD 20742
ABSTRACT
The evaluation of concentrated (wheel) load effects on a continuous orthotropic
plate supported on flexible supports is predicted by plate theory. In conjunction with
experimental tests, the results are applied in the development of a proposed design
criteria.
Introduction
During the past several years many
counties in the D. C. area were subjected
to severe flood damage. These floods
caused many bridge structures to be
washed out, subsequently creating a need
for the construction of bridges. In many
instances, the county highway people did
not want temporary structures. They
desired permanent structures, which
would be inexpensive and easily and
quickly erected by their personnel. Such
criteria can be met by using steel
I-girders in conjunction with steel bridge
planking, as shown in Fig. 1. In using
such planking the designer is faced with
a major design problem; that is, the
determination of the load distribution
factor for proper design of the longitudinal
girders. It is, therefore, the intention
of this paper to present a design recom-
mendation for such a factor by means
of analytical and experimental studies.
Present Criteria
At present the AASHO Specification
(1) does not identify the load distribution
factor for steel planking. In Section 1.3.1
76
of the Specification, reference is made
to a ‘‘Steel Grid’’ floor and states that
for two or more traffic lanes and the deck
thickness t < 4.0 inches, the distribution
factor is S/4.0. This specification would
probably be the most relevant; however,
a ‘‘Steel Grid’? does not resemble the
planking and may not give the same
distribution factor (S/4.0) as will be seen.
Analytical Studies
General
A bridge plank deck, as shown in Fig.
1, with typical details given in Fig. 2,
when interacting with longitudinal flex-
ible girders, can be considered an ortho-
tropic deck. The interaction of an
orthotropic deck with longitudinal girders
has been studied by Heins and Perry (3).
However, in their study, the main girders
were positioned transverse to the direc-
tion of traffic. The computer program
used in this study (3) can, however, be
readily applied in establishing the be-
havior of bridge planking and longitudinal
girders.
The analytical model is shown in Fig. 3,
with the planking spanning in the strong
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
direction between the girders. The model
will have two traffic lanes, span lengths
L = 10’, 20’, 30’, 40’, and S50’, and girder
spacing between 20” and 40”, as recom-
mended by a manufacturer of planking (2).
The selection of the girder stiffness was
obtained by first evaluating the induced
moment on one girder due to a set of truck
wheels, and evaluating the section modu-
lus. Also examined was the limiting
deflection (L/800) induced by a set of
wheels and determining the required stiff-
ness. This preliminary study resulted in
the girder sizes given in Table 1. Also
included in this table are the girder
spacings that were used as a function of
the bridge plank gage.
Bridge Plank Properties
1. Primary Stiffness D,
The primary moment of inertia stiff-
ness I, of a single cell, as shown in Fig.
4, is computed as a function of gage
thickness t and equals I, = 2.725t. The
inertia per unit of length for the
complete deck shown in Fig. 2 is
I, = 1.04 t/inch. The stiffness is, there-
ioe, equal to D, = El = E x 1.04t,
where B-— 29 x 10° ksi.
2. Minor Stiffness D,
The minor moment inertia I, was
evaluated considering two methods.
The first was to consider only a single
plate of thickness t, which gives I, = t?/
12(1 — yw”). If one considers the cor-
rugation to be sinusoidal, the stiffness
I, = .67t7/12(1 — pw”), as determined
by expressions given by Timoshenko
(4). The minimum value of I, will be
used in this study, thus the required
D, = Et?/1201 — p’).
2-3/8"
et ft .
Fig. 1. Bridge planking construction.
3. Torsional Stiffness H
The torsional stiffness of the plank-
ing can also be estimated by two
methods. The first is to assume the
stiffness equals the minor stiffness D,,
or to use the equation given by
Timoshenko (4), which gives H
= E(1.5)t?/12(1 — pw?). The minimum
value of H = D, will be used in this
study.
4. Final Stiffness
The resulting bridge plank stiff-
nesses for various gages are given in
Table 2. The parameter a and B, which
equal a — Hiv DID, GB = H/D,, ave
tabulated values required for the
computer input.
Girder Moments
Using the orthotropic computer pro-
gram (3), the behavior of the bridge
system consisting of the various girder
spacings, planking stiffness, and span
lengths subjected to two AASHO trucks
(1) was determined. The resulting maxi-
oa
a 24 5/8" ee
Cover Width
Fig. 2. Bridge plank section.
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
77
Siete 2 Lanes = 20' petite
Fig. 3. Bridge loading arrangement.
ment induced girder moments (M) were
then compared to the girder moment
induced in an isolated girder (Mgg)
subjected to a single set of truck wheels.
The ratio of M/Mg, to girder spacing were
then plotted, as shown in Fig. 5.
Distribution Factor
The plot of data shown in Fig. 5
actually represents the distribution factor
as used in the AASHO Specification (1).
The AASHO Specifications do not give
a distribution factor for planking; how-
ever, a D.F. for grid flooring is given
as S/4.0. Evaluating the D.F. for the
plot of data given in Fig. 5 is D.F.
= S/5S.0, which is not as restrictive as
S/4.0.
Table 1.—Bridge parameters.
Gage— Planking
7 Gage 10 Gage 12 Gage
Girder Girder Girder
Spacing Spacing Spacing Girder
Length S (in.) S (in.) S (in.) Size
10’ 34 29 26 Wi12 x 22
20’ 37 a2 29 W16 x 40
30’ 39 34 31 Wi18 x 85
40’ 43 38 35 W21 x 127
50’ 44 39 36 W24 x 180
78
Experiments
As described in the previous section
on ‘‘Bridge Plant Properties,’’ several
values for the stiffnesses can be com-
puted. In order to obtain some guidance
relative to the proper stiffness values, a
series of plate stiffness tests were con-
ducted.
The test specimens were cut from
typical planking samples of seven and
twelve gages. Three specimens of each
gage were tested in order to determine
the respective rigidities D,, D,, and H.
The test specimens are shown in Figs.
6 and 7 for each test configuration.
Similar tests on ribbed plates have
previously been described by Heins and
Hails (5) (6).
Primary Stiffness D,
As shown in Fig. 6(a) and 7(a), the
corrugation is positioned longitudinally
and loaded such that primary beam
bending moments are developed. In
the pure moment region a series of
deflectometers spaced at 6” were posi-
tioned beneath the specimen. Deflections
were recorded for each increment of
loading. The resulting plate stiffness
can then be readily determined by
applying the general difference equation:
M
—=y" =(y,-, — 2Y, bye ee
El y (Var y View (
where
dh = Longitudinal spacing between de-
flection points
n = Deflection point
Fig. 4. Typical plank cell.
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
M = Induced moment
EI = Plate stiffness
For the plate model shown in Fig. 6(a),
M =P x 24, ’} = 6”, Width = 24”, thus;
24P x 36
D, = EI/Width = —————_—_——___
(nei ae IA ae Yn+1)24
D, = EI/Width
fp 36P
(Vaan ah 2Yn “lis Yn+)
For each increment of load P up to
Prax = /000# (7 gage) and P,,, = 3000#
(12 gage), the y deflections were deter-
mined and the subsequent D, stiffness
determined as listed in Table 3 for the
7 and 12 gage specimens.
(2)
A
M/Mog
lio
Table 2.— Bridge plank stiffness.
Gage
Stiffness 7 Gage 10 Gage 12 Gage
D, 15.58 6.68 3.08
D,; 5100. 4070. 3162.
H 15.58 6.68 3.08
a 055 .0405 .03 1
B .003 1 .0016 .00097
Secondary Stiffness D,,
Shown in Figs. 6(b) and 7(b), the
corrugations are positioned transverse
to the supports. This type of arrangement
provides minimal stiffness and thus only
the dead load response was measured.
An equation similar to equation (1) was
2.0 3.0
Girder Spacing S-Ft.
Fig. 5. M./Mgg vs. girder spacing S.
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
79
Dd, Test Model
eae
=
Dy Test Model
H Test Model
Fig. 6. Test model details.
(c)
used in addition to the relationship
between load and deformation;
W/EI = y'’ = (Yn-2 — 4Yn-1
+ 6Yn a 4Ynt1 ag Yn+2)/r4 (3)
where W = Load per unit of length and
the other terms as previously described.
The total dead load of each specimen
was W,, = .172* (7 gage) and W,, = .102*
(12 gage). The deflection spacing was
equal to A = 6.0”. Applying Equation (1)
where M = WL?/8 and/or Equation (3),
the resulting stiffnesses were computed
as given in Table 3.
Torsion Stiffness H
Figs. 6(c) and 7(c) show the test
arrangement for subjecting a plate to pure
torsional moments. The relationship
between the induced moments and
distortion is given by;
4 O*w
OxOy
= H[(Var 7 Yor) va (Yai ra Yop /4n4 (4)
where the deflections y are measured
along the diagonal lines of the plate
referenced to the center at distances 6”
horizontal — 6” vertical, as shown in
Fig. 6(c). The induced moment (per
unit length) M,, = P/2, in which P,,,x
= 600# for 7 gage and P,,,, = 1004
for 12 gage.
The resulting torsional stiffness for
each model was computed and is given
in Table 3.
M,, =
Comparison
Table 3, in addition to listing the
experimental results, gives the theoretical
values as determined from expressions
given by Timoshenko (4) assuming a
sinusoidal corrugation and those selected
for the parametric study. In general,
the calculated primary stiffnesses D,
agree with the test data. The secondary
stiffnesses D, are off by a factor of
three and the torsional stiffnesses by a
factor of two. However, the important
parameters in conducting the computer
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
Fig. 7. Test model photograph.
study are a and B. As shown by Heins
and Perry (3), it is desirable to use a
minimum value of B, which was used.
Also a variation of a is not significant
providing the stiffness D, is in agreement
with the actual tests. Thus, the values
of a and B used in the parametric
81
Table 3.—Test results and theory.
7 Gage 12 Gage
Computer Computer
Stiffness Test Ref. (4) Value Test Ref. (4) Value
D, 5.46 10.50 15.58 1.03 2.06 3.08
D, 4545.0 5100. 5100. 2934. 3162. 3162.
H 31.65 23.40 15.58 8.07 4.6 3.08
a .202 101 .055 147 0595 .031
B .00696 .00459 .003 1 .00157 .00152 .00097
Zimmerman of Armco Steel Corporation,
who donated their time and material
relative to the test models.
study to develop the distribution factors
are valid.
Summary
The load distribution of steel bridge
planking over flexible girders, when
subjected to a series of AASHO wheel
loads, has been established as (S/5.0)
from a series of analytical studies. tion, Metals Product Division, Middletown,
A series of model tests was also Ohio, 1967.
conducted to determine the plate (3) C. P. Heins, P. Perry, “‘The Design of Floor
rigidity (D,, D,, and H) of 7 and 12 gage Beams in Orthotropic Bridge Floor Beams,”’
. a red Ty we eee Preprint ASCE National Structural Engr.
planking. Meeting, San Francisco, California, April,
1973.
S. Timoshenko, Theory of Plates and Shells ,
McGraw-Hill Publishing Company, New York,
References
(1) Standard Specifications for Highway Bridges,
AASHO, 11th Edition, Washington, D. C.,
1973.
(2) Armco Bridge Plank, Armco Steel Corpora-
Acknowledgments (4
—
The author wishes to express his
thanks to Graduate Students Mr. A.
Kurzwell, Mr. J. Oleinik, Mr. R. Krueger,
and Mr. K. Mantro, who performed, in
part, the analytical and experimental
studies; and also to Messrs. J. H.
Boynton, T. C. Phillips, and J. A.
82
(5)
~—
New York, 1955.
C. P. Heins, ‘“‘Behavior of a Stiffened Curved
Plate Model,’’ Preprint ASCE National Struc-
tural Engr. Meeting, Pittsburg, Pennsylvania,
April 1968.
(6) C. P. Heins, ‘‘Applied Plate Theory for the
Engineer,’ WLexington Books, Lexington,
Mass. 1976.
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
Drilled Human Teeth from the Coast of Ecuador
Douglas H. Ubelaker
Department of Anthropology, NUNH 342, Smithsonian Institution,
Washington, D. C. 20560
ABSTRACT
Dental mutilation of prehistoric human teeth is rare in Ecuador and confined to several
examples of gold inlays in young adults from the coastal provinces of Esmeraldas and
Guayas. A new example has now been found from the province of Los Rios which
further extends the geographic distribution of this custom. The example is the first
reported from an old adult and from a new location on the teeth.
The prehistoric aboriginal practice of
mutilation of the occlusal and _ labial
surfaces of anterior teeth apparently for
esthetic purposes is best known from
Middle America, where Romero (1970)
has identified over 1,000 examples. These
represent 7 distinct types ranging from
incisions and notches to drilled perfora-
tions with stone inlays. Farther south
in Ecuador, reported examples of pre-
historic dental mutilations are rare and
restricted to drilled perforations inlaid
with gold, all found on the coast in the
provinces of Guayas and Esmeraldas and
dating from the relatively recent Late
Integration period.
As early as 1913, Saville summarized
all known aboriginal dental inlays from
Ecuador: 3 poorly documented examples
from the area of Esmeraldas. He reported
perforations filled with gold discs on the
labial surfaces of the central maxillary
incisors of a skeleton from Atacames.
The skeleton was found in a ‘‘burial
tube’’ on the mght bank of the Rio
Atacames, just north of the town of that
name. The discs are located in the center
of the crowns’ labial surfaces and meas-
ure 6.5 and 5.0 mm in diameter.
Saville (1913:383) cites a second ex-
ample from the Esmeraldas area contain-
ing eight gold inlays in the maxillary
incisors and canines. His illustration of
the maxilla shows small circular inlays
near the occlusal edge of the labial
surface.
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
Saville’s final example from the Es-
meraldas area consists of gold inlays on
6 maxillary incisors and canines on an
isolated skull and mandible found at La
Piedra on the bank of the Esmeraldas
river at its junction with San Mateo
Bay. The teeth contain wide plates of
gold, measuring 5 x 8 mm, set into the
labial surface 1 mm or more.
More recently, Evans and Meggers
(1966:262) have reported an additional
example from a chimney-urn burial
within an artificial mound farther south,
in Guayas Province, Site G-M-S, Elisita
(Estrada, 1957:23; fig. 11-A). They illus-
trate small gold pegs with expanded
heads inserted into perforations of 2
incisors and a canine.
Recent examination of human remains
excavated by Meggers and Evans in 1961
from Guayas Province has revealed an
additional example. Fragmentary human
skeletal remains were recovered from a
mound urn burial, field cat. no. 1244,
La Compania Site (R-B-3), mound B, on
Rio Babahoyo, hacienda La Compania,
coastal Ecuador (unpublished). Associ-
ated artifacts suggest the site represents
the Milagro phase, Late Integration
period (Meggers, 1966:131—142). The
presence of European-manufactured arti-
facts in other areas of the site also
suggests alate date, perhaps 16th century
A. D. The urn burial producing the human
remains contained a considerable quantity
of gold, silver, copper, wood and textile
83
Fig. 1. Drilled teeth (in anatomical order) from La Compania Site, coastal Ecuador.
artifacts. Contact of the skeletal remains
with the copper artifacts produced con-
siderable copper staining on the bone.
The fragmentary skeletal remains rep-
resent at least 2 individuals: an adolescent
(10 to 15 years) and an adult (35 years+),
both of unknown sex. The adult is
represented only by 2 cervical vertebrae,
the left acromial process of a scapula
and 5 teeth. Both vertebrae display
osteophytic development corresponding
to Stewart’s (1958) stage two. The teeth
display extensive occlusal wear, with loss
of most of the crown and exposure of
the pulp cavity. In addition, all teeth
but the right lateral incisor display
circular, drilled perforations about 2.3
mm in diameter in the center of the
buccal surface of the crown, just above
the junction of the crown and root (fig. 1).
The perforations are about 2 mm deep.
Those on the central and right lateral
incisors are evenly drilled with sharp
borders. The perforation on the canine
is more irregular, with a sharp incisal
border but a roughened apical border.
In addition, a slight indentation occurs
84
at the same location on the left lateral,
just below an area where enamel has
been chipped away on the labial, occlusal
edge of the tooth.
It appears that this adult once had
drilled perforations on at least the 4
maxillary incisors and right maxillary
canine, probably for the purpose of
displaying inlays. The form of the per-
foration corresponds best with Romero’s
(1970:51) type El, although due to exten-
sive crown destruction, the possibility
of a more elaborate mutilation cannot
be ruled out.
The perforations are similar in size to
the circular inlays reported by Saville
(second example) and by Evans and
Meggers, except that the La Compania
perforations are located nearer the crown
root junction. In fact, this location
distinguishes the new example from
possibly all others reported in the New
World. Also, as Romero (1970:55) has
pointed out, nearly all other examples
occur on young adults, with minimal
dental attrition. This example is obviously
from a much older person, in which
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
attrition has destroyed nearly the entire
crown. It is quite possible that the
individual once displayed inlays located
more occlusally on the crown surface,
but lost them with advancing attrition,
and subsequently reperforated the teeth
on the remaining tooth stump. The con-
tinued display of the inlays may have
symbolized the status, which the exten-
sive and exotic accompanying grave
offerings strongly suggest this individual
enjoyed.
Acknowledgments
I thank Betty J. Meggers and Clifford
Evans for allowing me to document
this example prior to their publication
of the final site report. The specimens
discussed were collected by them in
August 1961, under Project J of the
Institute of Andean Research, supported
by a grant from the National Science
Foundation.
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
The photograph was prepared by
Victor Krantz of the Smithsonian Divi-
sion of Photographic Services.
References Cited
Estrada, Emilio. 1957. Ultimas Civilizaciones pre-
historicas de la Cuenca del Rio Guayas.
Museo Victor Emilio Estrada, No. 2.
Evans, Clifford, and Betty J. Meggers. 1966.
Mesoamerica and Ecuador. Handbook of Middle
American Indians 4(12): 243-264.
Meggers, Betty J. 1966. Ecuador. Praeger Pub-
lishers, New York.
Romero, Javier. 1970. Dental Mutilation, Trephina-
tion, and Cranial Deformation. Handbook of
Middle American Indians, R. Wauchope (Editor)
9(4): 50-67. University of Texas Press, Austin.
Saville, M. H. 1913. Pre-Columbian decoration of
the teeth in Ecuador with some account of the
occurrence of the custom in other parts of North
and South America. American Anthropologist
15: 377-394.
Stewart, T. D. 1958. The rate of development of
vertebral osteoarthritis in American whites
and its significance in skeletal age identification.
The Leech 28: 144-151.
85
ACADEMY AFFAIRS
THE AWARDS PROGRAM OF THE ACADEMY
AND RECENT HONOREES
The Annual Awards Dinner meeting of
the Academy was held on Thursday,
March 17, 1977 at the Cosmos Club. Four
research scientists and two _ science
teachers were recipients this Spring of
the Academy’s awards for outstanding
scientific achievement. A Special Award
was presented to Dr. Mary Louise
Robbins of the faculty at George Wash-
ington University.
In the area of research, the persons
honored were the following: Dr. James
H. Howard (Catholic University) for
Behavioral Sciences; Dr. Peter H. Fish-
man (National Institute of Neurological
and Communicative Diseases, NIH) for
Biological Sciences; Dr. Conrad P. Heins
(University of Maryland) for Engineering
Sciences; and Dr. Ming-Chang Lin
(Naval Research Laboratory) for Physical
Sciences.
For the area of Teaching of Science,
the Awardee at the college or university
level was Dr. J. David Lockard of the
Science Teaching Center and Botany
Department at the University of Mary-
land. The recipient of the Berenice G.
Lamberton Award for the Teaching of
High School Science was Mrs. Johanna
B. Donaldson, McLean High School,
McLean, Virginia.
The recipient of a Special Award of
the Academy was Dr. Mary Louise
Robbins, Professor of Microbiology in
the George Washington University. This
Special Award is a very broad one that
includes not only excellence and dedica-
tion to teaching, as adjudged by her
peers, but also meritorious public service
to science in the Washington Area and,
in this case, three foreign countries
(Egypt, Iraq, and Japan). According to
86
the records of the General Chairman of
the Awards Program (Dr. Kelso B.
Morris, who made the recommendation),
only two other persons in the past 25
years have been given this special
recognition. The six awards, as recom-
mended to the General Chairman by the
usual Panel Chairmen, and the Special
Award, were approved unanimously and
with deep appreciation by the Academy’s
Board of Managers.
Behavioral Sciences
Dr. James H. Howard, Associate
Professor of Psychology at The Catholic
University of America, was cited for
James H. Howard
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
‘‘his skillful experimentation on auditory
information processing and its cognitive
mechanisms.”’
He was born in Winchester, Mass.
In 1969, he completed the B.A. degree
magna cum laude with a Major in
Psychology from Providence College.
His Ph.D. in Psychology was completed
at Brown University in 1974. Member-
ships in professional and scientific soci-
eties include the American Psychological
Association, AAAS, Delta Epsilon Sigma,
and Sigma Xi.
The general area of Dr. Howard’s
work has been the analysis of cognitive
functioning within an information proc-
essing perspective. Dr. Howard’s ultimate
goal, as a target for a life’s work, is to
outline a theory of auditory pattern
recognition that would apply generally
to complex speech and non-speech
sounds. More immediately, he has con-
centrated on developing methods to
determine the psychologically important
characteristics for features of complex
non-speech sounds. In his view, until
such methods are outlined and tested,
we cannot hope to understand the proc-
esses involved in auditory recognition.
Biological Sciences
Dr. Peter H. Fishman, Research
Biochemist, NINCDS, National Institutes
of Health, was cited for “‘his contribu-
tions to the elucidation of gangliosides
as biotransducers of membrane-mediated
information.”’
He was born in Boston, Mass. He
completed the B.S. degree at Mas-
sachusetts Institute of Technology in
1961. His M.S. and Ph.D. degrees were
both earned at George Washington
University during the period 1965-1970.
Special honors held by him include mem-
bership in Sigma Xi and the Saunders
Teaching Fellowship at George Wash-
ington University.
In the six years since Dr. Fishman
joined the National Institutes of Health,
he has become a world-recognized au-
thority on the mechanism by which
environmental messages are received and
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
Peter H. Fishman
encoded into the functioning cells. This
signaling system involves the interaction
of circulating compounds in body fluids
such as thyroid-stimulating hormone,
chorionic gonadotropin, and luteinizing
hormone with specific substances on the
surface of cells known as gangliosides.
These specific substances were first
described over forty years ago. However,
only recently has significant progress
been made in understanding the function
of gangliosides, much of which is attrib-
utable to Dr. Fishman’s accomplish-
ments.
Engineering Sciences
Dr. Conrad P. Heins, Professor of
Civil Engineering at the University of
Maryland, was cited for ‘‘the develop-
ment of analytical or design specifications
for bridge structures.”’
He was born in Philadelphia, Penn-
sylvania. Earned degrees completed by
him are the following: BSCE, Drexel
Institute (June 1960); MSCE, Lehigh
University (June 1962); and Ph.D. Uni-
87
Conrad P. Heins
versity of Maryland, June 1967. Some
professional and scientific societies of
which he is a member are the ASCE,
ACI, SESA, IABSE, ASEE, Sigma Xi,
and Chi Epsilon.
Analytical techniques for use in the
study of complex bridge systems have
been developed by Dr. Heins. These
techniques have been used successfully
by engineers throughout the country, as
well as in England, Germany, Japan,
Iran, Spain, Brazil, Wales, Formosa,
Africa, Italy, Switzerland, France, Bel-
gium, Poland, and in other parts of
the world. He has just published two
textbooks, namely, ‘‘Bending and Tor-
sional Design in Structural Members”’
(1975) and ‘‘Applied Plate Theory for the
Engineer’ (1976). Both of these texts
incorporate original material developed
by Professor Heins. The torsion book
has received international acclaim. More-
Over, it was selected for the McGraw-
Hill BOOK-OF-THE-MONTH-CLUB.
Physical Sciences
Dr. Ming-Chang Lin, Head of the
Chemical Kinetics Section at the Naval
Research Laboratory, was cited for ‘‘the
discovery of new chemical lasers and the
outstanding application of lasers to
chemical problems.”’
88
Ming-Chang Lin
He was born in Hsinchu, Taiwan. His
B.S. degree was earned at National
Taiwan Normal University in 1959, and
his Ph.D. degree was earned at Ottawa
University in 1965. Dr. Lin is the author
of more than ninety (90) scientific papers
and talks in the areas of chemical kinetics
and chemical lasers. He was one of the
first scientists to recognize the great
potential of lasers in synthetic chemistry.
He suggested using a laser to activate a
specific chemical bond so that the reac-
tion would take place at that position.
Dr. Lin’s pioneering study in this area
involved the reaction of ozone and nitric
oxide.
For the years 1971 and 1974, he re-
ceived NRL’s Chemistry Division Award
for the best research papers originating
in that laboratory. In 1975, Dr. Lin was
the recipient of the Hillebrand Award
from the Chemical Society of Washington.
Teaching of Science
(College Level)
Dr. J. David Lockard, a Professor in
the Science Teaching Center and De-
partment of Botany at the University of
Maryland, was cited for his ‘‘outstanding
state, national, and international leader-
ship in science education.”’
He was born in Renovo, Pennsylvania.
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
|
J. David Lockard
At the Pennsylvania State University he
earned a B.S. degree in 1951; a M.Ed.
degree in 1955, and a Ph.D. (Botany) in
1962. Dr. Lockard has held the position
of Director of the Science Teaching
Center & the International Clearing
House on Science and Mathematics at
the University of Maryland since 1962.
Professional and scientific societies in
which he holds membership include the
following: AAAS (Fellow); Botanical
Society of America; Maryland Associa-
tion of Science Teachers; NSTA; Wash-
ington Academy of Sciences; and Sigma
Xi. In 1974, the National Science
Teachers Association awarded him a
citation for Distinguished Service to
Science Education.
Teaching of Science
(High School Level)
(The Berenice G. Lamberton Award)
Mrs. Johanna Bernice Donaldson, of
McLean High School (A Fairfax County,
Va., school) was cited as ‘‘an outstanding
teacher in earth sciences and pioneer
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
Johanna Bernice Donaldson
Mary Louise Robbins
89
in oceanic studies.’’ In May 1976, the
Joint Board on Science and Engineering
Education of the Greater Washington
Area honored Mrs. Donaldson with their
‘“Excellence in Teaching of Science’’
Award. On November 10, 1976, she
presented to all Fairfax County Area III
Principals a program on ‘‘The Importance
of Oceanic Studies and Implementing
Courses in Secondary Schools.”’
Public Service and Teaching of Science
Special Award
Dr. Mary Louise Robbins, Professor
of Microbiology in the George Washing-
ton University School of Medicine, was
cited for her intense dedication as a
superior teacher in the field of virology
at local, national, and _ international
levels and as one whose students are
carrying the torch of true science into
new and varied fields.
She was born in St. Paul, Minnesota.
Her training in science was received at
the following institutions: B.A. with
Major in Biology at The American
University, 1934; M.A. in Bacteriology
at the George Washington University,
1940; and Ph.D. in Bacteriology at The
George Washington University, 1944. In
1949, she received personal training in
virology at the Harvard Medical School,
Boston, Mass. under Monroe D. Eaton
and John F. Enders. For the period
1971-1972, she served as President of the
Washington Academy of Sciences. One
scientist has observed that it is amazing
that Dr. Robbins has found the time to
publish 52 research papers (including 17
abstracts) and still enrich her courses
with materials from most of those articles.
Among her students, one can list the
following who found her to be a most
inspiring teacher: Dr. Anne Bourke; Dr.
Kenneth Takamoto; Dr. Janet Hartley;
Dr. Ariel Hollingshead; and Dr. Daniel
Kundin. Dr. Robbins holds membership
in ten professional organizations and is
listed in nine biographical publications.
NEW FELLOWS
Ronald W. Manderscheid, Research
Sociologist, National Institute of Mental
Health, HEW., in recognition of his work
in social psychology, and in particular
his theoretical work on the social and
psychological effects of micro-physical
environments, his research on alienation,
and his contribution to empirical assess-
ments of mental health interventions.
Sponsor: Richard H. Foote.
Phillip E. Sokol, President, Gillette
Res. Institute, in recognition of his
contribution to cosmetic science, in
90
particular his studies of keratin chemistry,
polymer syntheses and application, and
novel dye syntheses and application.
Sponsors: Charles A. Rader, Norman
R. Hollies.
F. Christian Thompson, Research
Entomologist, USDA., in recognition of
his studies on the biogeography of
insects, and in particular his research
on the taxonomy and systematics of the
fly family Syrphidae. Sponsors: Richard
H. Foote, Ashley B. Gurney.
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
|
OBITUARIES
Patricia A. Sarvella
Dr. Patricia A. Sarvella, 50, a research
geneticist for the Agricultural Research
_ Service in Beltsville, died on March 8,
1977, of cancer in Prince Georges County
Hospital. She lived on Dove Circle in
Laurel, Md.
Dr. Sarvella was executive vice pres-
ident of the Organization of Professional
Employes of the Department of Agricul-
ture, associate director and awards
chairman of the Prince Georges Science
Fair Association, lieutenant governor of
District 16 of Pilot Club International and
a former president of the American
Association of University Women’s med-
ical division. She was program chairman
of the Washington Academy of Sciences.
A native of Waukeegan, Ill., Dr.
J. WASH. ACAD. SCI., VOL. 67, NO. 2, 1977
Sarvella held a B.S. degree from Case-
Western University and a Ph.D. in
genetics from North Carolina State
University. She also studied in Sweden
and Washington State University and
taught at Mississippi State University.
She leaves a brother, John R., of
Alexandria.
L. Edwin Yocum
Dr. L. Edwin Yocum, 86, died at his
home in Clearwater, Florida on 23.
February 1977. A plant physiologist, he
taught botany at George Washington
University for 25 years and was head of
the Botany Department there for 8 years.
He had been retired for 25 years at the
time of his death. Interment was in
Pennsylvania.
91
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paw
| VOLUME 67
| Journal of the serteninl Ge
WASHINGTON
ACADEMY. SCIENCES
Issued Quarterly
at Washington, D.C.
Diréctory sue
CONTENTS
Directory, 1977:
Directory of The NC AG SUN ete iets OE, | ie hae cae
PuphHabenical WiStiNe) ”.ol..-b ites ee ves Se Ga ee oe
Information on the Newly Affiliated Societies ...........
Washington Academy of Sciences
EXECUTIVE COMMITTEE
President
Richard H. Foote
President-Elect
Mary H. Aldridge
Secretary
Kelso B. Morris
a
Treasurer
Alfred Weissler
Members at Large
George Abraham
Grover C. Sherlin
BOARD OF MANAGERS
All delegates of affiliated
Societies (see facing page)
EDITOR
Richard H. Foote
EDITORIAL ASSISTANT
Elizabeth Ostaggi
ACADEMY OFFICE
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Telephone: (301) 530-1402
Founded in 1898
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|
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SeaLAME TATE NCES Ol: VV ASHIIPLOM) a. open Goss cic a 2S ee wo 5014 de ies © Wis weele ee eens caw eens Conrad B. Link
PSM AIMETICAN POFEStEES. 6.052665 os Sek cb ecu eek owe eh e ee wesc wees Thomas B. Glazebrook
Um aMIIMEIC LY (OMENPINECES 00 ck ec alee ee ae ee gece ek eee nee Fede eevee’ George Abraham
Menmermenicetncal and EIECtrOMmicS MMBINCETS. 62... 205 oy sec de eee eee ew shoes nd George Abraham
Pence meseciciyion Mechanical EPNQMee:rs 22... ek ce ee cee cece esc wcensvaas Michael Chi
Paaannmomcical SOcIety Of WaSDINSION 2... 2... ee ee oi caw ace c estan cvees Robert S. Isenstein
eee NCIC ETO MICTODIONOLY , 222 oaks oe Sos etn on tes eMac bo ec ec eee ne eon eei™ Michael Pelzcar
Mae GEermMeCtHCAn WVinkitary ENPINGEIS 2... oa ec ee ce ke ew a ee wees cet ececeees H. P. Demuth
Pe ICH, Oliv EP MPINCELS, 2625.25 .iik noi cbt s oe ce ee oe lene Dace cena cwes Robert Sorenson
faacwionexpenmental Biology and Medicine ....:2.5........ 500. c cece cece cee ceene Donald Flick
Se ARMS OTE EN ERE WIENS 66 2 cos hc cs ok ng hc o's 6 oo OS dis be via alee wleW vyis agivaad wed Glen W. Wensch
Meciiaional Association of Dental Research ..........60.00c0se cs ercccceeee William V. Loebenstein
POmenican imstituce of Acronautics‘and Astronautics ..2.......2.0.0. cece cece cece cnnee George J. Vila
ee UA PICAL SOLICLY | aoc) ki cic soe scl eo vin oe Oe Crp te Gidle.n cfs cielo ee eee e es A. James Wagner
ee ere te EEC Or WaASMINGTON 9.6 2 eel cc oie cece ese dee ed eeseaseccasvuseer Robert J. Argauer
See MEIC NY Ol ATMCTICA: 25. o.5.2 aor Sac jaurienw seo sre di ob an oad ewes ee es ee bbe ee Delegate not appointed
EGE UU SRST SSVCCCt es NA ME AL er eee CPM ine Ois ane ica aa a) Dick Duffey
eee OEOADETCCHIIOIOLIS(S . 5... sc ss ss oe wiclsie he sides es See bubee ccc e se ceeses William Sulzbacher
ee eee CE SOIC EM ec aria ee ee tien eA Stones alceteer ce cS SEY Wieters «0. a wirdane se BONES © Inactive
en aM ESSENCE LP he ee sees 3 Seale nels mines Sek © a ee Bale ko 0's Delegate not appointed
i PPMeE MSN I SCICNCe. CMID 0.2 onc x asctiha sie Gad, 2 nse a eS Beeb d eee ee ewe we Inactive
mei ssacianon of Physics Teachers. 2.20.1 2.54 Aisles. aes Peete eee ee eee To be appointed
eee PTE SXMECRE VT CUNC Dw ees so ee cal es oa Svan ala ew ie BU & eco wm NOIR Grand 6 aaa eos Lucy B. Hagan
Pian sOcicey Of Plant Physiologists’ so... ocs% ces eee eed salen ee eee ee eee eee ne Walter Shropshire
Serenerusn Operations mesearcn COUNCIL 2.2. 50.65 bee ee Cee ee tcl tesa eens John G. Honig
Pee MEIBLICM LG AMeCICd: if). coc faa Secs Seis se sgt ole sere Walls Wale le aw sale ees va ee eS Inactive
American Institute of Mining, Metallurgical
SEE PEI Sry Tid By EYE TST a ld i lg aml lt te ta eh i Ne a Philip W. Guild
eT DUEGIVASELOMOUICES, i) iciofiseis slevs s lesors te als SGN anki cate ae wie BEN ew ee oe Benson J. Simon
EMAC AMASSOCIGHON OF ATNEMCA Gear es foes Seb cbs cae ole d sce ee eae eee eeecs cen Patrick Hayes
SHALE OIC NERUSIS, Yoh ic 3b GS). oe eteain a aye oa wi ale ele ek de we eee Miloslav Recheigl, Jr.
DEES ENGIOOICAl ASSOCIANION re bo ee FP ode Bee ee ee Pot Ce ease eenben ees John O’ Hare
Re ASMInPioOnveaiit LeGhnical Group), nj. ..c.- + ies 0 0% 0: 6'5j0 0 rece opwinice coe be eeeeie eee’ Paul G. Campbell
Pee Mey OpAthOlGPiCal SOCIELY. ..cd06's)oha Su a Es Palen ele wee Rcjelale Slay iele nig ea sa Tom van der Zwet
Peerionyerr GencraliSyStemis RESCarCh” 12.56... 6. ee ace cet eee eens Ronald W. Manderscheid
cam NAM SEL PUNE SS AE PBN 5 ea ae nh ote yee, bin, snl dnd ns was nase x R'm we Hele Sl Ope). H. McIlvaine Parsons
Delegates continue in office until new selections are made by the representative societies.
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977 93
THE DIRECTORY OF THE ACADEMY FOR 1977
Foreword
The present, 52nd issue of the Academy’s direc-
tory is again this year issued as part of the Septem-
ber number of the Journal. As in previous years,
the alphabetical listing is based on a postcard
questionnaire sent to the Academy membership.
Members were asked to update the data concerning
address and membership in affiliated societies by
June 30, 1977. In cases in which cards were not
received by that date, the address appears as it was
used during 1977, and the remaining data were
taken from the directory for 1976. Corrections
should be called to the attention of the Academy
office.
Code for Affiliated Societies, and Society Officers
1 The Philosophical Society of Washington (1898)
Harold Glaser, 312 Chartwell Dr., Silver Spring, MD. 20904
George T. Armstrong, 1401 Dale Dr., Silver Spring, MD. 20910
James F. Goff, 3405 34th Pl., N.W., Washington, D.C. 20016
President:
Vice-President:
Secretary:
Delegate: James F. Goff
2 Anthropological Society of Washington (1898)
President:
President-elect:
20016
Secretary:
Delegate:
Priscilla Reining, 3601 Rittenhouse St., N.W. Washington, D.C. 20016
Ruth Lardman, Dept. of Anthropology, American Univ., Washington, D.C.
Mary F. Gallager, Montgomery College, Rockville, MD. 20853
Jean K. Boek, National Graduate Univ., 3408 Wisconsin Ave., N.W.,
Washington, D.C. 20016
3 Biological Society of Washington (1898)
W. Duane Hope, Dept. of Invertebrate Zoology, National Museum of
Natural History, Smithsonian Institutions, Washington, D.C. 20560
President: Richard S. Cowan
Vice-President: Clyde F. E. Roper
Secretary:
Delegate:
William R. Heyer, Amphibian & Reptiles, Nat. History Bldg., Smithsonian
Institution, Washington, D.C. 20560
4 Chemical Society of Washington (1898)
President:
Vice-President:
Secretary:
Delegate: David H. Freeman
5 Entomological Society of Washington (1898)
President:
President-elect:
Secretary:
John R. Moody, NBS, Chem. Bldg., 222, Washington, D.C. 20375
David H. Freeman. Univ. of Md. College Park, MD. 20742
George Mushrush, George Mason Univ. Fairfax, VA. 22030
Maynard J. Ransay, Rm. 660, Federal Bldg., Hyattsville, MD. 20782
Douglas W. S. Sutherland, 125 Lakeside Dr. Greenbelt, MD. 20770
Donald R. Whitehead, Rm. W-619, U.S. National Museum of Natural
History, Washington, D.C. 20560
Delegate: Maynard J. Ramsay
6 National Geographic Society (1898)
President:
Chairman:
Secretary:
Delegate:
Robert E. Doyle, National Geographic Society, Washington, D.C. 20036
Melvin M. Payne, National Geographic Society, Washington, D.C. 20036
Owen R. Anderson, National Geographic Society, Washington, D.C. 20036
T. Dale Stewart, Smithsonian Institution, Museum of Natural History,
Washington, D.C. 20560
7 Geological Society of Washington (1898)
President: _
Francis R. Boyd, Jr., Carnegie Institution of Washington, Geophysical
Lab., 2801 Upton St., N.W., Washington, D.C. 20008
Vice-President:
J. Thomas Dutro, U.S. Geological Survey, Branch of Paleontology and
Stratigraphy, U.S. National Museum, Washington, D.C. 20560
Secretary:
Stop 973
Delegate:
94
William E. Davies, U.S. Geological Survey, Reston, Va. 22092, Mail
Marian M. Schnepfe, 2019 Eye St. N.W. #402, Washington, D.C. 20006
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
8 Medical Society of the District of Columbia (1898)
President: William S. McCune
President-elect: Frank S. Bacon
Secretary: Thomas Sadler
Delegate: Not appointed
9 Columbia Historical Society (1899)
President: Wilcomb E. Washburn, Amer. Studies, S.I., Washington, D.C. 20560
Vice-President: William H. Press, 1511 K St., N.W., Washington, D.C. 20005
Secretary: Marcellina Hummer, 2006 Columbia Rd., N.W., Washington, D.C. 20009
Delegate: Paul H. Oehser, National Geographic Society, Washington, D.C. 20036
10 Botanical Society of Washington (1902)
President: Laurence E. Skog, Smithsonian Institution, Dept. of Botany, Washington,
D.C. 20560
Vice-President: Erik A. Neumann, U.S. National Arboretum, 28th & M Sts., N.W.,
Washington, D.C. 20002
Secretary: James J. White, Dept. of Botany, Smithsonian Institution, Washington,
D.C. 20560
Delegate: Conrad B. Link, Univ. of Md., Dept. of Horticulture, College Park,
Md. 20742
11 Society of American Foresters, Washington, Section (1904)
Chairman: Arthur V. Smith, 3301 Wessynton Way, Alexandria, Va. 22309
Chairman-elect: Richard T. Marks, Rte. 2, Warrenton, Va. 22186
Secretary: Ann E. Carey, 3620 Suitland Rd., Washington, D.C. 20020
Delegate: T. B. Glazebrook, 7809 Bristow Dr., Annandale, Va. 27007
12 Washington Society of Engineers (1907)
President: Dean Harold Liebowitz, Sch. of Engineering, George Washington Univ.,
Washington, D.C. 20052
Vice-President: Jeffrey H. Rumbaugh, Potomac Electric Power Co., 1900 Pennsylvania
Ave., N.W., Washington, D.C. 20068
Secretary: John A. Waring, 8502 Flower Ave., Takoma Park, Md. 20012
Delegate: George Abraham, 3107 Westover Dr., S.E., Washington, D.C. 20020
13 Institute of Electrical & Electronics Engineers, Washington Section (1912)
Chairman: _Dennis Bodson, 233 North Columbus St., Arlington, Va. 22203
Vice-Chairman: Horst W. A. Gerlach, 4521 Cheltenham Dr., Bethesda, Md. 20014
Secretary: Sajjad Durrani, 175 Lafayette Dr., Olney, Md. 20832
Delegate: George Abraham, 3107 Westover Dr., S.E., Washington, D.C. 20020
14 American Society of Mechanical Engineers, Washington Section (1923)
Chairman: Michael Chi, 2721 24th St. N., Arlington, Va. 22207
Vice-Chairman: Robert L. Hershey, 1255 New Hampshire Ave., N.W., Apt. 433,
Washington, D.C. 20036
Secretary: Ron Niebo, 8587 Brae Brook Dr., Lanham, Md. 20801
Delegate: Michael Chi
15 Helminthological Society of Washington (1923)
President: Kendall G. Powers, Food & Drug Adm., Bldg. 320-A, BARC-East,
Beltsville, Md. 20705
Vice-President: Harley G. Sheffield, Lab. of Parasitic Diseases, NIH, NOAID, Bldg. 5,
Bethesda, Md. 20014
Secretary: J. Ralph Lichtenfels, Animal Parasitology Inst., Bldg. 1080, BARC-East,
Beltsville, Md. 20705
Delegate: Robert S. Isenstein, Animal Patasitology Inst., Bldg. 1040, BARC-East,
Beltsville, Md. 20705
16 American Society for Microbiology, Washington Branch (1923)
President: June A. Bradlaw, Food & Drug Adm., Genetic Toxicology Branch,
; HFF-156, Washington, D.C.20204
Vice-President: Irvin C. Mohler, The George Washington University School of Medicine,
Dept. of Medical & Public Affairs, Washington, D.C. 20037
Secretary: Phyllis D. Kind, The George Washington University School of Medicine,
Dept. of Microbiology, Washington, D.C. 20037
Delegate: Michael J. Pelczar, Jr., Vice President for Graduate Studies & Research,
University of Md., College Park, Md. 20742
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977 95
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19
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21
22
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25
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Society of American Military Engineers, Washington Post (1927)
President: Capt. Thomas F. Stallman, Code 04, NAVFAC Hdatrs., 200 Stovall St.,
Alexandria, Va. 22332
Vice-President: Col. Rodney Cox, DAEN-FEZ-B, Washington, D.C. 20314
Secretary: Lt. Jim Delkar, Code 0632, NAVFAC Hdatrs., 200 Stovall St., Alex-
andria, Va. 22310
Delegate: Hal P. Demuth, 4025 Pine Brook Rd., Alexandria, Va. 22310
American Society of Civil Engineers, National Capital Section (1942)
President: James W. Harland, 1511 K St., N.W., Suite 337, Washington, D.C. 20005
Vice-President: Norman L. Cooper, Dept. of Transportation, 400 7th St., Rm. 9422, Washing-
ton, D.C. 20590
Secretary: Robert Efimba, Dept. of Civil Engineering, Howard University,
Washington, D.C. 20059
Delegate: Robert Sorenson, Coastal Engineering Research Ctr., Kingman Bldg.,
Ft. Belvoir, Va. 22060
Society for Experimental Biology & Medicine, D.C. Section (1952)
President: Juan C. Penhos, Dept. of Physiology & Biophysics, Georgetown Univ.
School of Med. & Dentistry, Washington, D.C. 20007
President-elect: Cyrus R. Creveling, 4516 Amherst Lane, Bethesda, Md. 20014
Secretary: Marvin Bleiberg, 3613 Old Post Rd., Fairfax, Va. 22030
Delegate: Donald F. Flick, 930 19th St., So., Arlington, Va. 22202
American Society for Metals, Washington Chapter (1953)
Chairman: Klaus M. Zwilsky, U.S. Atomic Energy Comm., Washington, D.C. 20545
Vice-Chairman: Alan H. Rosenstein, Air Force Office of Scientific Res., 1400 Wilson Blvd.,
Arlington, Va. 22209
Secretary: Joseph Malz, NASA, Code RWM, Washington, D.C. 20546
Delegate: Glen W. Wensch, U.S. Atomic Energy Comm., Washington, D.C. 20545
International Association for Dental Research, Washington Section (1953) '
President: Donald W. Turner, Dental Sciences Dept., Naval Med. Res. Inst., NNMC,
Bethesda, Md. 20014
Vice-President: John D. Termine, Natl. Institute of Dental Research, Bethesda, Md. 20014
Secretary: William R. Cotton, Naval Medical Research Institute, Bethesda, Md. 20014
Delegate: William V. Loebenstein, National Bureau of Standards, Washington, D.C.
20234
American Institute of Aeronautics and Astronautics, National Capital Section (1953)
Chairman: Paul J. Waltrup, John Hopkins University, Applied Physics Lab., Johns
Hopkins Rd., Laurel, Md. 20810
Vice-Chairman: Robert O. Bartlett, Goddard Space Flight Ctr., Greenbelt, Md. 20771
Secretary: George J. Vila, General Dynamics, 1025 Conn. Ave., N.W., Washington,
D.C. 20036
Delegate: George J. Vila
American Meteorological Society, D.C. Chapter (1954)
Chairman: Thomas D. Potter, Environmental Data Serv. DXI, Page Bldg. No. 2,
Washington, D.C. 20235
Vice-Chairman: Celso Barrientos, Natl. Weather Serv. W427, 821 Gramax Bldg., 8060
13th St., Silver Spring, Md. 20910
Secretary: Richardson Decker, SPO/Natl. Weather Serv., Gramax Bldg., 8060 13th
St., Silver Spring, Md. 20910
Delegate: A. James Wagner, National Weather Service, World Weather Bldg.,
5200 Auth Rd., Washington, D.C. 20233
Insecticide Society of Washington (1959)
Chairman: Neal O. Morgan, USDA, ARS, Bldg. 476, Rm. 100, BARC-East, Belts-
ville, Md. 20705
Chairman-elect: Jack R. Plimmer, USDA, ARS, Bldg. 306, Rm. 313, BARC-East, Belts-
ville, Md. 20705
Secretary: ~ John Neal, ARS, ARC, Bldg. 467, Beltsville, Md. 20705
Delegate: Robert Argauer, ARS, ARC, Bldg. 309, Beltsville, Md. 20705
Acoustical Society of America (1959)
Chairman: John A. Molino, Sound Section, NBS, Washington, D.C. 20234
Vice-Chairman: Charles T. Molloy, 2400 Claremont Dr., Falls Church, Va. 22043
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
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Secretary: William K. Blake, Naval Ship R & D Ctr., Bethesda, Md. 20034
Delegate: None appointed
American Nuclear Society, Washington Section (1960)
President: B. E. Leonard, Institute for Resource Management, 4948 St. Elmo Ave.
Bethesda, Md. 20014
Vice-President: Ray Durante, Westinghouse Electric, 1801 K St., N.W., Washington,
D.C. 20006
Secretary: S. Bassett, NUS Corp., Rockville, Md. 20852
Delegate: Dick Duffy, Nuclear Engineering, Univ. of Md., College Park, Md. 20742
Institute of Food Technologists, Washington Section (1961)
Chairman: Tannous Khalil, Giant Foods, Inc., Landover, Md. 20785
Vice-Chairman: Florian C. Majorack, Food & Drug Adm., Washington, D.C.
Secretary: Glenn V. Brauner, National Canners Assoc., Washington, D.C. 20036
Delegate: William Sulzbacher, 8527 Clarkson Dr., Fulton, Md. 20759
American Ceramic Society, Baltimore-Washington Section (1962)
Chairman: W. T. Bakker, General Refractories Co., P.O. Box 1673, Md. 21203
Chairman-elect: L. Biller, Glidden-Dirkee Div., SCM Corp., 3901 Hawkins Point Rd.,
Baltimore, Md. 21226
Secretary: Edwin E. Childs, J. E. Baker Co., 232 E. Market St., York, Pa. 17405
Delegate: None appointed
Electrochemical Society, National Capital Section (1963)
Chairman: Judith Ambrus, Naval Surface Weapons Ctr., White Oak, Md. 20910
Vice-Chairman: John B. O’Sullivan, 7724 Glenister Dr., Springfield, Va. 22152
Secretary: John Ambrose, NBS, Washington, D.C. 20234
Delegate: None appointed
Washington History of Science Club (1965)
Chairman: Richard G. Hewlett, Atomic Energy Comm.
Vice-Chairman: Deborah Warner, Smithsonian Institution
Secretary: Dean C. Allard
Delegate: None appointed
American Association of Physics Teachers, Chesapeake Section (1965)
President: William Logan, D.C. Teachers College, 2565 Georgia Ave., Washington,
D.C. 20001
Vice-President: Eugenie V. Mielczarek, George Mason Univ., 4400 University Dr.,
Fairfax, Va. 22030
Secretary: John B. Newman, Towson State College, Towson, Md. 21204
Delegate: None appointed
Optical Society of America, National Capital Section (1966)
President: Lucy B. Hagan, National Bureau of Standards, Rm. B360, Physics Bldg.,
Washington, D.C. 20234
Vice-President: M. Kent Wilson, 1800 G. St., N.W., Rm. 518, Washington, D.C. 20006
Secretary: L. Douglas Ballard, Bldg. 226, Rm. 317, National Bureau of Standards,
Washington, D.C. 20234
Delegate: Lucy B. Hagan
American Society of Plant Physiologists, Washington Section (1966)
President: Dale G. Blevins, Dept. of Botany, Univ. of Md., College Park, Md. 20742
Vice-President: Anne H. Datko, NIMH Bldg. 32A, Rm. 101, Bethesda, Md. 20014
Secretary: Werner J. Meudt, USDA, ARS, Beltsville, Md. 20705
Delegate: W. Shropshire, Jr., Smithsonian Institution, 12441 Parklawn Dr., Rockville,
Md. 20852
Washington Operations Research Council (1966)
President: Gerald R. McNichols, 8101 Rondelay Lane, Fairfax Station, Va. 22039
Vice-President: Charles Tiplitz, 8809 Bells Mills Rd., Potomac, Md. 20854
Secretary: Thomas Sicilia
Delegate: John G. Honig, 7701 Glenmore Spring Way, Bethesda, Md. 20034
Instrument Society of America, Washington Section (1967)
President: Francis C. Quinn
President-elect: John I. Peterson
Secretary: Frank L. Carou
Delegate: None appointed
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977 97
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American Institute of Mining, Metallurgical & Petroleum Engineers (1968)
Chairman: Gus H. Goudarzi, U.S. Geological Survey, Natl. Ctr., Mail Stop 920.
Reston, Va. 22092
Vice-Chairman: Garrett R. Hyde, U.S. Bureau of Mines, College Park Metallurgy Res.
Ctr., College Park, Md. 20740
Secretary: Ronald A. Munson, U.S. Bureau of Mines, Division of Metallurgy, 2401 E.
St., N.W., Washington, D.C. 20241
Delegate: Phil W. Guild, U.S. Geological Survey, Natl. Ctr., Mail Stop 952,
Reston, Va. 22092
National Capital Astronomers (1969)
President: Benson J. Simon, 8704 Royal Ridge Lane, Laurel, Md. 20811
Vice-President: Geoffrey Hornseth, 8806 W. Fort Foote Terrace, Oxon Hill, Md. 20022
Secretary: William R. Winkler, 15804 Pinecroft Lane, Bowie, Md. 20716
Delegate: _ Benson J. Simon
Maryland-District of Columbia and Virginia Section of Mathematical Assoc. of America (1971)
President: Orville Thomas, 110 McKendoce Ave., Annapolis, Md. 21401
Secretary: Reuben Drake, 3701 Connecticut Ave., N.W., Washington, D.C. 20008
Delegate: Patrick Hayes, 950 25th St. N.W., Washington, D.C. 20037
D.C. Institute of Chemists (1973)
President: Kelso B. Morris, 1448 Leegate Rd., N.W., Washington, D.C. 20012
President-elect: Leo Schubert, 8521 Beech Tree Rd., Bethesda, Md. 20034
Secretary: Fred D. Ordway, 2816 Fall Jax Dr., Falls Church, Va. 22042
Delegate: Milosiav Rechcigl, Jr., 1703 Mark Lane, Rockville, Md. 20852
The D.C. Psychological Association (1975)
President: Richard P. Youniss, Dept. of Psychology, Catholic Univ., Washington,
D.C. 20064
Vice-President: John F. Borriello, St. Elizabeth’s Hospital, Overholser Division,
Washington, D.C. 20032
Secretary: Eugene Stammeyer, St. Elizabeth’s Hospital, Overholser Division,
Washington, D.C. 20032
Delegate: John J. O’ Hare, Office of Naval Research, 800 N. Quincy St., Arlington, Va.
22017)
The Washington Paint Technical Group (1976)
President: David T. Bloodgood, Bethlehem Steel Corp., CTD Shipbuilding, Sparrows
Point, Md. 21219
Vice-President: Leon S. Birnbaum, 5117 Kenwood Dr., Annandale, Va. 22003
Secretary: Mildred A. Post, National Bureau of Standards, Bldg. 226, Rm. B-348
Washington, D.C. 20234
Delegate: Paul G. Campbell, National Bureau of Standards, B-348 Br., Washington,
D.C. 20234
Potomac Division, American Phytopathological Society (1977)
President: F. M. Latterell, Plant Disease Lab., USDA, P.O. Box 1209, Frederick, Md.
21701
Vice-President: C. W. Roane, Dept. of Plant Path., Va. Polytech. Inst., Blacksburg, Va. 24061
Secretary: J. R. Stavely, Tobacco Lab., USDA, BARC-West, Beltsville, Md. 20705
Delegate: Tom van der Zwet, USDA, Fruit Lab., Rm. 12, Bldg. 004, BARC-West,
Beltsville, Md. 20705
Metropolitan Washington Chapter of the Society for General Systems Research (1977)
Chairman: Ronald W. Manderscheid, 212 West Montgomery Ave., Rockville, Md.
20850
Delegate: Ronald W. Manderscheid
Potomac Chapter, Human Factors Society (1977)
President: Harry J. Older, 3527 Saylor Place, Alexandria, Va. 22304
President-elect: Dean M. Havron, Human Sciences Research Inc., 7710 Old Springhouse
Rd., McLean, Va. 22101
Secretary: Marshall A. Narva, 2 Infield Court, South, Rockville, Md. 20854
Delegate: H. Mcllvaine Parsons, Institute for Behavioral Res., Inc., Silver Spring,
Md. 20910
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
Alphabetical List of Members
M = Member; F = Fellow; E = Emeritus member L = Life Fellow. Numbers in parentheses refer to
numerical code in foregoing list of affiliated societies.
A
ABELSON, PHILIP H., Ph.D., Carnegie Inst. of
Washington, Carnegie Institution of Washing-
ton, 1530 P St., N.W., Washington D.C. 20005
(F-1, 4, 7, 16)
ABRAHAM, GEORGE, M.S., Ph.D., 3107 West-
over Dr., S.E., Washington, D.C. 20020 (F-1,
Bi2, 13, 31, 32)
ACHTER, M. R., Code 6416, U.S. Naval Research
Lab., Washington, D.C. 20375 (F-20, 36)
ADAMS, CAROLINE L., 242 North Granada St.,
Arlington, Va. 22203 (E-10)
ADLER, SANFORD C., 14238 Briarwood Terr.,
Rockville, Md. 20853 (F-1)
ADLER, VICTOR E., 8540 Pineway Ct., Laurel,
Md. 20810 (F-5, 24)
ADRIAN, FRANK J., Applied Phys. Lab., Johns
Hopkins Univ., Laurel, Md. 20810 (F)
AFFRONTI, LEWIS, Ph.D., Dept. of Microbiology,
George Washington Univ. Sch. of Med., 2300
Eye St., N.W., Washington, D.C. 20037
(F-16, 19)
AHEARN, ARTHUR J., Ph.D., 9621 East Bexhill
Dr., Box 294, Kensington, Md. 20795 (F-16)
AKERS, ROBERT P., Ph.D., 9912 Silverbrook Dr.,
Rockville, Md. 20850 (F-6)
ALBUS, JAMES S., 4515 Saul Rd., Kensington,
Md. 20014 (F)
ALDRICH, JOHN W., Ph.D., 6324 Lakeview Dr.,
Falls Church, Va. 22041 (F)
ALDRIDGE, MARY H., Ph.D., Dept. of Chemistry,
American University, Washington, D.C. 20016
4)
ALEXANDER, ALLEN L., Ph.D., 4216 Sleepy
Hollow Rd., Annandale, Va. 22003 (F-4)
ALEXANDER, BENJAMIN, Ph.D., Pres., Chicago
State Univ., 95th St. at King Dr. Chicago Ill.
(F)
ALGERMISSEN, S. T., 5079 Holmes PI., Boulder,
Colo. 80303 (F)
ALLEN, ANTON M., D.V.M., Ph.D., 11718 Lake-
way Dr., Manassas, Va. 22110 (F)
ALLEN, FRANCES J., Ph.D. 7507 23rd Ave.,
Hyattsville, Md. 20783 (F)
ALTER, HARVEY, Ph.D., Nat. Center for
Resource Recovery, Inc., 1211 Connecticut
Ave., N.W., Washington, D.C. 20036 (F-4)
ANDERSON, JOHN D., Jr., Ph.D., Dept. Aerospace
Eng., Univ. Maryland, College Park, Md.
20742 (F-6, 22)
ANDERSON, MYRON S., Ph.D., 1433 Manchester
Lane, N.W., Washington, D.C. 20011 (F-4)
ANDERSON, WENDELL L., Rural Rt. 4, Box 4172,
La Plata, Md. 20646 (F-4)
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
ANDREWS, JOHN S., Sc.D., 10314 Naglee Rd.,
Silver Spring, Md. 20903 (F-15)
ANDRUS, EDWARD D., BS., 1600 Rhode Island
Ave., N.W., Washington, D.C. 20036 (M-7, 25)
APOSTOLOU, Mrs. GEORGIA L., B.A. 1001
Rockville Pike, #424, Rockville, Md. 20852
(M-4)
APSTEIN, MAURICE, Ph.D., 4611 Maple Ave.,
Bethesda, Md., 20014 (F-1, 6, 13)
ARGAUER, ROBERT J., Ph.D., 4208 Everett St.,
Kensington, Md. 20795 (F-24)
ARMSTRONG, GEORGE T., Ph.D., 1401 Dale Dr.,
Silver Spring, Md. 20910 (F-1, 4)
ARONSON, C. J., 3401 Oberon St., Kensington,
Md. 20910 (M-1, 32)
ARSEM, COLLINS, 10821 Admirals Way,
Potomac, Md. 20854 (M-1, 6, 13)
ASLAKSON, CARL I., 5707 Wilson Lane, Be-
thesda, Md. 20014 (E)
ASTIN, ALLEN V., Ph.D., 5008 Battery Lane,
Bethesda, Md. 20014 (E-1, 13, 22, 35)
AXILROD, BENJAMIN M., Ph.D. 9915 Marquette
Dr., Bethesda, Md. 20034 (E-1)
AYENSU, EDWARD, Ph.D., 510 H. St., N.W.,
Washington, D.C. 20024 (F-3, 6, 10)
BAILEY, R. CLIFTON, Ph.D., 6507 Divine St.,
McLean, Va. 22101 (F)
BAKER, ARTHUR A., Ph.D., 5201 Westwood Dr.,
N.W., Washington, D.C. 20016 (E-7)
BAKER, LOUIS C. W., Ph.D., Dept. of Chemistry,
Georgetown University, N.W., Washington,
D.C. 20007 (F-4)
BALLARD, LOWELL D., 722 So. Colonial, Ster-
ling, Va. 22170 (F-1, 6, 13, 32)
BARBROW, LOUIS E., Natl. Bureau of Standards,
Washington, D.C. 20234 (F-1, 13, 32)
BARGER, GERALD L., Ph.D., 17 West Blvd. N.,
Columbia, Mo. 65201 (F-23)
BARNHART, CLYDE S., Sr., Rt. 4, Box 207A,
Athens, Ohio 45701 (F)
BEACH, LOUIS A., Ph.D., 1200 Waynewood
Blvd., Alexandria, Va. 22308 (F-1, 6)
BECKER, EDWIN D., Ph.D., Inst. Arthritis & Meta-
bolic Dis., Bldg. 2 Rm. 122, National Institutes
of Health, Bethesda, Md. 20014 (F-4)
BECKETT, CHARLES W., 5624 Madison St.,
Bethesda, Md. 20014 (F-1, 4)
BECKMANN, ROBERT B., Ph.D., Dept. of Chem.
Engineering, Univ. of Md., College Park, Md.
20742 (F-4)
99
BElJ, HILDING, K., 69 Morningside Dr., Laconia,
NH 03246 (L-1)
BEKKEDAHL, NORMAN, Ph.D., 405 N. Ocean
Blvd., Apt. 1001, Pompano Beach, Fla. (E)
33062 (E)
BELLANTI, JOSEPH A., Ph. D., 6007 Carewood
Lane Bethesda, Md. 20016 (F-6, 10)
BELSHEIM, ROBERT, Ph.D., 2475 Virginia Ave.
#514, Washington, D.C. 20037 (F-1, 12, 14,
25)
BENDER, MAURICE, Ph.D., 1303 22nd Ave., Rock
island, Il. 61201 (F)
BENESCH, WILLIAM, Inst. for Molecular Physics,
Univ. of Maryland, College Park, Md. 20742
(F-1, 32)
BENJAMIN, C. R., Ph.D., IPD/ARS, USDA, Rm.
459, Federal Bg., Hyattsville, Md. 20782
(F-6, 10, 42)
BENNETT, BRADLEY F., 3301 Macomb St., N.W.,
Washington, D.C. 20008 (F-1, 20)
BENNETT, JOHN A., 7405 Denton Rd., Bethesda
Md. 20014 (F, 20)
BENNETT, MARTIN TOSCAN, Ch.E., 3700 Mt.
Vernon Ave., Rm. 605, Alexandria, Va. 22305
(F-4, 6)
BENNETT, WILLARD H., Box 5342, North
Carolina State Univ., Raleigh, N.C. 27607 (E)
BENSON, WILLIAM, Ph.D., 618 Constitution
Ave., N.E., Washington, D.C. 20002 (M-32, 44)
BERGMANN, OTTO, Ph.D., Dept. Physics, George
Washington Univ., Washington, D.C. 20052
(F-1)
BERLINER, ROBERT W., M.D., Dean, Yale
School of Medicine, New Haven, Conn. 06510
(F)
BERNETT, MARIANNE K., Code 6170, Naval Res.
Lab., Washington, D.C. 20375 (M-4)
BERNSTEIN, BERNARD, M.S., 7420 Westlake
Terr., #608, Bethesda, Md. 20034 (M-25)
BERNTON, HARRY S., 4000 Cathedral Ave.,
N.W., Washington, D.C. 20016 (F-8)
BERRY, Miss ARNEICE O., 5108 Hayes St.,
N.E., Washington, D.C. 20019 (M)
BESTUL, ALDEN B., 9400 Overlea Ave., Rock-
ville, Md. 20850 (F-1, 6)
BICKLEY, WILLIAM E., Ph.D., Dept. of
Entomology, Univ. of Md., College Park,
Md. 20742 (F-5, 24)
BIRD, H. R., Animal Science Bg., Univ. of Wis-
consin, Madison, Wisc. 53706 (F)
BIRKS, L. S., Code 6480, U.S. Naval Research
Lab., Washington, D.C. 20375 (F)
BLAKE, DORIS H., A.M., 3416 Glebe Rd., North
Arlington, Va. 22207 (E-5)
BLANK, CHARLES A., Ph.D., 5110 Sideburn Rad.,
Fairfax, Va. 22030 (M-4, 7, 39)
BLOCK, STANLEY, Ph.D., National Bureau of
Standards, Washington, D.C. 20234 (F-4)
BLUNT, ROBERT F., 5411 Moorland Lane,
Bethesda, Md. 20014 (F)
BOEK, JEAN K., Ph.D., Natl. Graduate Univ., 3408
Wisconsin Ave., N.W., Washington, D.C.
20016 (F-2)
BOGLE, ROBERT W., Code 53071, Naval Res.
100
Lab., 991 Skylark Dr., La Jolla, Cal. 92037
(F)
BONDELID, ROLLON O., Ph.D., Code 6640, Naval
Research Lab., Washington, D.C. 20375 (F)
BORGESEN, KENNETH G., M.A., 3212 Chillum
Rd. #302, Mt. Rainier, Md. 20822 (M)
BOTBOL, J. M., 2301 November Lane, Reston,
Va. 22901 (F)
BOWLES, R. E., Ph.D., 2105 Sondra Ct., Silver
Spring, Md. 20904 (F-6, 14, 22, 35)
BOWMAN, THOMAS E., Ph.D., Dept. Invert.
Zoology, Smithsonian Inst., Washington,
D.C. 20560 (F-3)
BOZEMAN, F. MARILYN, Div. Virol., Bur.
Biologics, FDA, 8800 Rockville Pike, Rock-
ville, Md. 20014 (F-16, 19)
BRADY, ROBERT F., Jr., Ph.D., 706 Hope Lane,
Gaithersburg, Md. 20760 (F-4, 41)
BRANCATO, E. L., M.S., Code 4004, U.S. Naval
Research Lab., Washington, D.C. 20390 (F-6,
13)
BRANDEWIE, DONALD F., 6811 Field Master Dr.,
Springfield Va. 22153 (F)
BRAUER, G. M., Dental Research A-123 Polymer,
Natl. Bureau of Standards, Washington, D.C.
20234 (F-4, 21)
BREGER, IRVING A., Ph.D., 212 Hillsboro Dr.,
Silver Spring, Md. 20902 (F-4, 6, 7, 39)
BREIT, GREGORY, Ph.D., 73 Allenhurst Rd.,
Buffalo, N.Y. 14214 (E-13)
BRENNER, ABNER, Ph.D., 7204 Pomander Lane,
Chevy Chase, Md. 20015 (F-4, 6, 29)
BRICKWEDDE, F. G., 104 Davey Lab., Dept. of
Physics, Pennsylvania State Univ., University
Park, Pa. 16802 (L-1)
BRIER, GLENN W., A.M., Dept. Atmosph. Sci.,
Colorado State Univ., Ft. Collins, Colo.
80523 (F-23)
BROADHURST, MARTIN G., 504 Blandford St.,
Apt. 4, Rockville, Md. 20850 (F)
BROMBACHER, W. G., 17 Pine Run Community,
Doylestown, Pa. 18901 (E-1, 35)
BROOKS, RICHARD C., Ph.D., 6221 N. 12th St.,
Arlington, Va. 22205 (M-13, 34)
BROWN, RUSSELL G., Ph.D., Dept. of Botany,
Univ. of Maryland College Park, Md. (F)
BROWN, THOMAS, McP., 2465 Army-Navy
Dr., Arlington, Va. 22206 (F-8, 16)
BRUCK, STEPHEN D., Ph.D., 1113 Pipestem PI.,
Rockville, Md. 20854 (F-4, 6, 39)
BURAS, EDMUND M.., Jr., M.S., Gillette Research
Inst., 1413 Research Blvd., Rockville, Md.
20850 (F-4, 6, 39)
BURGER, ROBERT J., (COL. M.S.) 5307 Chester-
field Dr., Camp Springs, Md. 20031 (F-6, 22)
BURGERS, J. M., Prof. D.Sc., 4622 Knox Road,
Apt. 7, College Park, Md. 20740 (F-1)
BURK, DEAN, Ph.D., 4719 44th St.,
Washington, D.C. 20016 (E-4, 19, 33)
BURNETT, H. C., Metallurgy Division, Natl.
Bureau of Standards, Washington, D.C.
20234 (F)
BYERLY, PERRY, Ph.D., 5340 Broadway Terr.,
#401, Oakland, Calif. 94618 (F)
N.W.,
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
BYERLY, T. C., Ph.D., 6-J Ridge Rd., Greenbelt,
Md. 20770 (F-6, 19)
C
CALDWELL, FRANK R., 4821 47th St., N.W.,
Washington, D.C. 20016 (E-1, 6)
CALDWELL, JOSEPH M., 2732 N. Kensington St.,
Arlington, Va. 22207 (E-18)
CAMERON, JOSEPH M., A345 Physics Bldg.,
Natl. Bureau of Standards, Washington, D.C.
20234 (F-1)
CAMPAGNONE, ALFRED F., P.E., 9321 Warfield
Rd., Gaithersburg, Md. 20760 (F)
CAMPBELL, LOWELL E., B.S., 10100 Riggs Rd.,
Adelphi, Md. 20783 (F-12, 13)
CAMPBELL, PAUL G., Ph.D., 3106 Kingtree St.,
Silver Spring, Md. 20902 (F-4, 41)
CANNON, E. W., Ph.D., 5 Vassar Cir., Glen Echo,
Md. 20768 (F-1, 6)
CANTELO, WILLIAM W., Ph.D., 11702 Wayneridge
St., Fulton, Md. 20759 (F-6, 24)
CARNS, HARRY R., Bg. 001, Agr. Res. Cent. (W.),
USDA, Beltsville, Md. 20705 (M-10, 33)
CARROLL, Miss KAREN E., 11565 N. Shore Dr.,
#21A, Reston, Va. 22090 (M)
CARROLL, WILLIAM R., 4802 Broad Brook Dr.,
Bethesda, Md. 20014 (F)
CARTER, HUGH, 2039 New Hampshire Ave.,
N.W., Washington, D.C. 20009 (E)
CASH, EDITH K., 505 Clubhouse Rd., Bingham-
ton, N.Y. 13903 (E-10)
CASSEL, JAMES M., Ph.D., 12205 Sunnyview Dr.,
Germantown, Md. 20767 (F-4, 21)
CHANEY, JAMES G., Rt. 2, Box 232L, Sotterley
Hghts., Hollywood, Md. 20636 (M)
CHAPLIN, HARVEY P., Jr., 1561 Forest Villa
Lane, McLean, Va. 22101 (F-22)
CHAPLINE, W. R., 4225 43rd St.,
Washington, D.C. 20016 (E-6, 10, 11)
CHEEK, CONRAD H., Ph.D., Code 8330, U.S.
Naval Res. Lab., Washington, D.C. 20375 (F-4)
CHERTOK, BENSON T., Ph.D., Dept. of Physics,
American Univ., Wash. D.C. 20016 (M-1)
CHEZEM, CURTIS G., Ph.D., 3295 River Rd.,
Eugene, Oregon 97404 (F)
CHI, MICHAEL, Sc.D., Civil-Mech. Engr. Dept.,
Catholic Univ., Washington, D.C. 20064
(F-14)
CHOPER, JORDAN J., 121 Northway, Greenbelt,
Md. 20770 (M)
CHRISTIANSEN, MERYL N., Ph.D., Chief Plant
Stress Lab. USDA ARS, Beltsville, Md.
20705 (F-6, 33)
CHURCH, LLOYD E., D. D. S., Ph.D., 8218 Wis-
consin Ave., Bethesda, Md. 20014 (F-1, 6, 9,
1955211)
CLAIRE, CHARLES N., 4403 14th St., N.W.,
Washington, D.C. 20011 (F-1, 12)
CLARK, FRANCIS E., ARS Research Lab., P.O.
Box E, Ft. Collins, Colo. 80521 (F)
N.W.,
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
CLARK, GEORGE E., Jr., 4022 North Stafford
St., Arlington, Va. 22207 (F)
CLARK, JOAN ROBINSON, Ph.D., U.S. Geologi-
cal Survey, 345 Middlefield Rd., Menlo Park,
Calif. 94025 (F-7)
CLEEK, GIVEN W., 5512N. 24th St., Arlington, Va.
22205 (M-4, 28, 32)
CLEMENT, J. REID, Jr., 3410 Weltham St.,
Suitland, Md. 20023 (F)
CLEVEN, GALE W., Ph.D., RD. 4, Box 334B,
Lewistown, Pa. 17044 (F-1)
COATES, JOSEPH F., Off. of Tech Assessment
U.S. Congress Wash. D.C. 20510 (F-1, 2, 4)
COHN, ROBERT, M.D., 7221 Pyle Road, Be-
thesda, Md. 20034 (F-1)
COLE, KENNETH S., Ph.D., National Institutes
of Health, Bethesda, Md. 20014 (F-1)
COLE, RALPH I., 3431 Blair Rd., Falls Church,
Va. 22041 (F-12, 13, 22)
COLLINS, HENRY B., Dept. Anthropology,
Smithsonian Inst., Washington, D.C. 20560
(E-2)
COLWELL, R. R., Ph.D., Dept. of Microbiology,
Univ. of Maryland, College Park, Md. 20742
(F-1, 16)
COMPTON, W. DALE, Ford Motor Co., P.O.
Box 1603, Dearborn, Mich. 48121 (F)
CONGER, PAUL S., M.S., Dept. of Botany, U.S.
National Museum, Washington, D.C. 20560
(E)
CONNORS, PHILIP I., 12909 Two Farm Dr.,
Silver Spring, Md. 20904 (F-6, 31)
COOK, RICHARD K., Ph.D., 8517 Milford Ave.,
Silver Spring, Md. 20910 (F-1, 25)
COONS, GEORGE H., Ph.D., % Dr. J. E. Dees,
413 Carolina Circle, Durham, N.C. 27707
(E-10)
COOPER, KENNETH W., Ph.D. Dept. Biol., Univ.
of California, Riverside, Cal. 92521 (F-5)
CORLIS, EDITH L. R., Mrs., 2955 Albemarle
St. N.W., Washington, D.C. 20008 (F)
CORLISS, JOHN O., Ph.D., 9512 E. Stanhope
Rd., Kensington, Md. 20795 (F-6)
CORNFIELD, JEROME, G.W.V. Biostat-Ctr., 7979
Old Georgetown Rd., Bethesda, Md. 20014
(F)
COSTRELL, LOUIS, Chief 240. 03, Natl. Bureau
of Standards, Washington, D.C. 20234 (F)
COTTERILL, CARL H., M.S., U.S. Bureau of Mines
2401, E. St., N.W., Washington, D.C. 20241
(F-36)
COYLE, THOMAS D., National Bureau of Stand-
ards, Washington, D.C. 20234 (F-4, 6)
CRAFTON, PAUL A., P.O. Box 454, Rockville,
Md. 20850 (F)
CRAGOE, CARL S., 6206 Singleton Place,
Bethesda, Md. 20034 (E-1)
CRANE, LANGDON T., Jr., 7103 Oakridge Ave.,
Chevy Chase, Md. 20015 (F-1, 6)
CREITZ, E. CARROLL, 10145 Cedar Lane, Ken-
sington, Md. 20795 (E-32)
CROSSETTE, GEORGE, 4217 Glenrose St., Ken-
sington, Md. 20795 (M-6, 17)
101
CULBERT, DOROTHY K., 812 A St., S.E., Wash-
ington, D.C. 20003 (M-6)
CULLINAN, FRANK P., 4402 Beechwood Rad.,
Hyattsville, Md. 20782 (E-6, 10, 33, 42)
CULVER, WILLIAM H., Ph.D., 2841 Chesapeake
St., N.W., Washington, D.C. 20008 (M-1, 32)
CURRAN, HAROLD R., Ph.D., 3431 N. Randolph
St., Arlington, Va. 22207 (E-16)
CURRIE, CHARLES L., S.J., President, Wheeling
College, Wheeling, W.Va. 26003 (F)
CURTIS, ROGER, W., Ph.D., 6308 Valley Rd.,
Bethesda, Md. 20034 (F)
CURTISS, LEON F., 1690 Bayshore Drive, Eng-
lewood, Fla. 33533 (E-1)
CUTHILL, JOHN R., Ph.D., 12700 River Rd.,
Potomac, Md. 20854 (F-20, 36)
CUTKOSKY, ROBERT D., 19150 Roman Way,
Gaithersburg, Md. 20760 (F-13)
D
DARRACOTT, HALVOR T., M.S., 3325 Mansfield
Rd., Falls Church, Va. 22041 (F-13, 34, 38)
DAVIS, CHARLES M., Jr., Ph.D., 8458 Portland
Pl., McLean, Va. 22101 (M-1, 6, 25)
DAVIS, MARION MACLEAN, Ph.D., Apt. 100,
Crosslands, Kennett Square, Pa. 19348
(L-4, 6)
DAVIS, R. F., Ph.D., Chairman, Dept. of Dairy
Science, Univ. of Maryland, College Park,
Md. 20742 (F)
DAVISSON, JAMES W., Ph.D., 400 Cedar Ridge
Dr., Oxon Hill, Md. 20021 (F-1)
DAWSON, ROY C., Ph.D., 7002 Chansory Lane,
Hyattsville, Md. 20782 (E-16)
DAWSON, VICTOR C. D., 9406 Curran Rd., Silver
Spring, Md. 20901 (F)
DEAL, GEORGE E., D.B.A., 6245 Park Road,
McLean, Va. 22101 (F-34)
DE BERRY, MARIAN B., 3608 17th St., N.E.,
Washington, D.C. 20018 (M)
DEDRICK, R. L., Bg. 13, Rm. 3W13, NIH,
Bethesda, Md. 20014 (F-1)
DE VOE, JAMES R., 17708 Parkridge Dr., Gai-
thersburg, Md. 20760 (F-4, 6)
DE WIT, ROLAND, Metallurgy Division, Natl.
Bureau of Standards, Washington, D.C.
20234 (F-1, 6, 36)
DELANEY, WAYNE R., The Wyoming Apts., 111,
2022 Columbia Rd., N.W., Washington, D.C.
20009 (M-6, 9, 32)
DEMUTH, HAL P., MSEE, 4025 Pinebrook Rad.,
Alexandria, Va. 22310 (F-13, 17)
DENNIS, BERNARD K., 915 Country Club Dr.,
Vienna, Va. 22180 (F)
DERMEN, HAIG, Ph.D., Plant Industry Station,
Beltsville, Md. 21250 (F)
DESLATTES, RICHARD D., Jr., 610 Aster Blvd.,
Rockville, Md. 20850 (F)
DETWILER, SAMUEL B., Jr., 631 S. Walter Reed
Dr., Arlington, Va. 22204 (F-4, 39)
DEVIN, CHARLES, Ph.D., 629 Blossom Dr.,
Rockville, Md. 20850 (M-25, 31)
102
DI MARZIO, E. A., 14205 Parkvale Rd., Rockville,
Md. 20853 (F)
DIAMOND, J. J., Physics B-150, Natl. Bureau of
Standards, Washington, D.C. 20234 (F-4, 28)
DICKSON, GEORGE, M.A., Dental and Med.
Materials Sect., National Bureau of Stand-
ards, Washington, D.C. 20234 (F-6, 21)
DIEHL, WILLIAM W., Ph.D., 200 Maple Ave., Falls
Church, Va. 22046 (E-3, 4)
DIGGES, THOMAS G., 3900 N. Albemarle St.,
Arlington, Va. 22207 (E-20)
DIMOCK, DAVID A., 4800 Barwyn House Rad.,
#114, College Park, Md. 20740 (M-13)
DIXON, PEGGY A., Ph.D., 422 Hillsboro Dr., Silver
Spring, Md. 20902 (F)
DOCTOR NORMAN, B.S., 3814 Littleton St.,
Wheaton, Md. 20906 (F-13)
DOFT, FLOYD S., Ph.D., 6416 Garnett Drive, Ken-
wood, Chevy Chase, Md. 20015 (E-4, 6, 19)
DONALDSON, JOHANNA B., Mrs., 3020 North
Edison St., Arlington, Va. 22207 (F)
DONNERT, HERMANN J., Ph.D., RFD 4, Box 136,
Terra Heights, Manhattan Ks. 66502 (F)
DONOVICK, RICHARD, Ph.D., 16405 Alden Ave.,
Gaithersburg, Md. 20760 (F-6, 16, 19)
DOUGLAS, CHARLES A., Ph.D., Sec. 221.12,
Natl. Bureau of Standards, Washington, D.C.
20234 (F-4)
DOUGLAS, THOMAS B., Ph.D., 3031 Sedgwick
St., N.W., Washington, D.C. 20008 (F-4)
DRAEGER, R. HAROLD, M.D., 1201 N. 4th Ave.,
Tucson, Ariz. 85705 (E-32)
DRECHSLER, CHARLES, Ph.D., 6915 Oakridge
Rd., University Park (Hyattsville), Md. 20782
(E-6, 10)
DUBEY, SATYA D., Ph.D., 7712 Groton Rd.,
Bethesda, Md. 20034 (F)
DUERKSEN, J. A., B.A., 3134 Monroe St., N.E.
Washington, D.C. 20018 (E-1, 6, 38)
DUFFEY, DICK, Ph.D., Nuclear Engineering,
Univ. Maryland, College Park, M.D. 20742
(F-26)
DUNKUM, WILLIAM W., M.S., 3503 Old Dominion
Bivd., Alexandria, Va. 22305 (F-31)
DU PONT, JOHN ELEUTHERE, P.O. Box 358,
Newtown Square, Pa. 19073 (M)
DUPRE, ELSIE, Mrs., Code 5536A, Optical Sci.
Div., Naval Res. Lab., Washington, D.C. 20390
(F-32)
DURIE, EDYTHE G., 5011 Larno Dr., Alexandria,
Va. 22310 (F)
DURRANI, S. H., Sc.D., 17513 Lafayette Dr.,
Olney, Md. 20832 (F-13, 22)
DURST, RICHARD A., Ph.D., Chemistry Bldg. Rm.
A 221, Natl. Bur. of Standards, Washington,
D.C. 20234 (F-4, 6)
DYKE, E. D., 173 Northdown Rd., Margate, Kent,
England (M)
E
EASTER, DONALD, Inst. Gas Technology, 1825
K St., N.W., Washington, D.C. 20006 (M)
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
EDDY, BERNICE E., Ph.D., 6722 Selkirk Ct.,
Bethesda, Md. 20034 (E-6, 16)
EGOLF, DONALD R., 3600 Cambridge Court,
Upper Marlboro, Md. 20870 (F-10)
EISENBERG, PHILLIP, C.E., 6402 Tulsa Lane,
Bethesda, Md. 20034 (M-14, 22, 25)
EISENHART, CHURCHILL, Ph.D., Met B-268,
National Bureau of Standards, Washington,
D.C. 20234 (F-1, 30, 38)
EL-BISI, HAMED M., Ph.D., 135 Forest Rd., Millis,
Ma. 02054 (M-16)
ELLINGER, GEORGE A., 739 Kelly Dr., York, Pa.
17404 (E-6)
ELLIOTT, F. E., 7507 Grange Hall Dr., Oxon Hill,
Md. 20022 (E)
EMERSON, K. C., Ph.D., 2704 Kensington St.,
Arlington, Va. 22207 (F)
EMERSON, W. B., 415 Aspen St., N.W., Wash-
ington, D.C. 20012 (E)
ENNIS, W. B., Jr., Ph.D., Agricultural Res. Ctr.
U. of Florida, 3205 S.W. 70th Ave., Ft. Lauder-
dale, Fl. 33314 (F-6)
ETZEL, HOWARD W., Ph.D., 7304 Riverhill Rd.,
Oxon Hill, Md. 20021 (F-6)
EWERS, JOHN C., 4432 26th Rd., N, Arlington,
Va. 22207 (F-2, 6)
i
FAHEY, JOSEPH J., U.S. Geological Survey,
Washington, D.C. 20242 (E-4, 6, 7)
FAN, SHOU SHAN, 20427 Aspenwood Lane,
Gaithersburg, Md. 20760 (F-18)
FARROW, RICHARD P., 2911 Northwood Dr.,
Alameda, Ca. 94501 (F-4, 6, 27)
FATTAH, JERRY, 3451 S. Wakefield St., Arling-
ton, Va. 22206 (M-4, 39)
FAULKNER, JOSEPH A., 1007 Sligo Creek Pky.,
Takoma Park, Md. 20012 (F-6)
FAUST, GEORGE 1T., Ph.D., P.O. Box 411,
Basking Ridge, NJ 07920 (F-9)
FAUST, WILLIAM R., Ph.D., 5907 Walnut St.,
Temple Hills, Md. 20031 (F-1, 6)
FAYER, RONALD, Ph.D., USDA ARS Animal Para-
sitology |, Beltsville, Md. 20705 (M-15)
FEARN, JAMES E., Ph.D., Materials and Com-
posites Sect., Natl. Bureau of Standards,
Washington, D.C. 20234 (F-4, 6)
FELDMAN, SAMUEL, NKF Engr. Associates,
Inc., 8720 Georgia Ave., Silver Spring, Md.
20910 (M-6, 25)
FELSHER, MURRAY, Ph.D., NASA Code Ek.,
Wash. D.C. 20546 (M-1, 7)
FERRELL, RICHARD A., Ph.D., Dept. of Physics,
University of Maryland, College Park, Md.
20742 (F-6, 31)
FIFE, EARLH., Jr., M.S., Box 122, Royal Oak, Md.
21662 (E-6, 16, 19)
FILIPESCU, NICOLAE, M.D., Ph.D., 4836 S. 7th
St., Arlington, Va. 22204 (F-4)
FINN, EDWARD J., Ph.D., 4211 Oakridge La.,
Chevy Chase, Md. 20015 (F-1, 6, 31)
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
FISHER, JOEL L., 5602 Asbury Ct., Alexandria,
Va. 22313 (M)
FISHMAN, PETER H., Ph.D., 3333 University
Blvd. West, Kensington, Md. 20795 (F)
FLETCHER, DONALD G., Natl. Bureau of Stand-
ards, Rm. A102, Bldg. 231-IND, Washington,
D.C. 20234 (M-4)
FLICK, DONALD F., 930 19th St. So., Arlington,
Va. 22202 (F-4, 19, 39)
FLINN, DAVID R., 8104 Bernard Dr., Ft. Washing-
ton, Md. 20022 (F-4, 29)
FLORIN, ROLAND E., Ph.D., Polymer Stab. and
React. Sect., B-318, National Bureau of
Standards, Washington, D.C. 20234 (F-4, 7)
FLYNN, DANIEL R., Ph.D., 17500 Ira Court,
Derwood, Md. 20855 (F-4)
FLYNN, JOSEPH H., Ph.D., 5309 Iroquois Rd.,
Bethesda, Md. 20016 (F-4)
FOEKLER, HERBERT, MSLS., 10710 Lorain
Ave., Silver Spring, Md. 20901 (M-22, 43)
FONER, S. N., Applied Physics Lab., The Johns
Hopkins University, 11100 Johns Hopkins
Rd., Laurel, Md. 20810 (F-1)
FOOTE, RICHARD H., Sc.D., 8807 Victoria Road,
Springfield, Va. 22151 (F-5, 6)
FORZIATI, ALPHONSE F., Ph.D., 9812 Dameron
Dr., Silver Spring, Md. 20902 (F-1, 4, 29)
FORZIATI, FLORENCE H., Ph.D., 9812 Dameron
Dr., Silver Spring, Md. 20902 (F-4)
FOSTER, AUREL O., 4613 Drexel Rd., College
Park, Md. 20740 (E-15, 24)
FOURNIER, ROBERT O., 108 Paloma Rd., Por-
tola Valley, Calif. 94025 (F-6, 7)
FOWELLS, H. A., Ph.D., 3858 N. Hemlock PI.,
Oak Harbor, Wa. 98277 (E-6, 11)
FOWLER, EUGENE, Int. Atomic Energy Agency,
Kartner Ring 11, A-1011, Vienna, Austria
(M-26)
FOWLER, WALTER B., M.A., Code 673, Goddard
Space Flight Center, Greenbelt, Md. 20771
(M-32)
FOX, DAVID W., The Johns Hopkins Univ.,
Applied Physics Lab., Laurel, Md. 20810 (F)
FOX, WILLIAM B., 1813 Edgehill Dr., Alexandria,
Va. 22307 (F-4)
FRANKLIN, PHILIP J., 5907 Massachusetts Ave.
Extended, Washington, D.C. 20016 (F-4, 13,
39)
FRANZ, GERALD J., M.S., Box 695, Bayview,
Id. 83803 (F-6, 25)
FREEMAN, ANDREW F., 5012 N. 33rd. St., Arling-
ton, Va. 22207 (M)
FREDERIKSE, H. P. R., Ph.D., 9625 Dewmar
Lane, Kensington, Md. 20795 (F)
FRENKIEL, FRANCOIS N., Code 1801.2, Naval
Ship Res. & Develop. Ctr., Bethesda, Md.
20084 (F-1, 22, 23)
FRIEDMAN, MOSHE, 4511 Yuma St., Washing-
ington, D.C. 20016 (F)
FRIESS, S.L., Ph.D., Environmental Biosciences
Dept., Naval Med. Res. Inst. NNMC, Bethesda,
Md. 20014 (F-4, 39)
FRUSH, HARRIET L., 4912 New Hampshire Ave.,
103
N.W., Apt. 104, Washington, D.C. 20011
(F-4, 6)
FULLMER, IRVIN H., Lakeview Terrace, P.O. Box
100, Altoona, Fla. 32702 (E-1, 6, 14)
FULTON, ROBERT A., 530 Merrie Dr., Corvallis,
Oregon 97330 (E-4, 5, 24)
FURUKAWA, GEORGE T., Ph.D. National Bureau
of Standards, Washington, D.C. 20234 (F-1,
4, 6)
FUSILLO, MATTHEW H., 2600 Brinkley Rd., Oxon
Hill, Md. 20022 (M)
G
GAFAFER, WILLIAM M., 133 Cunningham Dr.,
New Smyrna Beach, Fla. 32069 (E)
GAGE, WILLIAM, Ph.D., 2146 Florida Ave., N.W.,
Washington, D.C. 20008 (F-2)
GALLER, SIDNEY, 6242 Woodcrest Ave., Balti-
more, Md. 21209 (F)
GALTSOFF, PAUL S., Ph.D., 15 Jacque Loeb
Rd., Woods Hole, Mass. 02543 (E)
GALVIN, CYRIL J., Jr., 7728 Brandeis Way,
Springfield, Va. 22153 (F-7, 18, 30)
GANT, JAMES O., Jr., M.D., 4349 Klingle St., N.W.
Wash. D.C. 20016 (M)
GARNER, C. L., The Garfield, 5410 Connecticut
Ave., N.W., Washington, D.C. 20015 (E-1, 4,
12, 17, 18)
GARVIN, DAVID, Ph.D., 18700 Walker’s Choice
Rd., Apt. 519, Gaithersburg, Md. 20760 (F-4)
GUANAURD, GUILLERMO C., Ph.D., 4807 Macon
Rd., Rockville, Md. 20852 (M-6, 25)
GHAFFARI, ABOLGHASSEN, Ph.D., D.Sc., 5420
Goldsboro Rd., Bethesda, Md. 20034 (L-1,
38)
GHOSE, RABINDRA N., Ph.D., LL.B., 8167 Mul-
holland Terr., Los Angeles Hill, Calif. 90046
(F-13, 22)
GIACCHETTI, ATHOS, Dept. Sci. Affairs, OAS,
1735 Eye St., N.W., Washington, D.C. 20006
(M-32)
GIBSON, JOHN E., Box 96, Gibson, N.C. 28343
(E)
GIBSON, KASSON S., 4817 Cumberland St.,
Chevy Chase, Md. 20015 (E)
GINTHER, ROBERT J., Code 6445, U.S. Naval
Res. Lab., Washington, D.C. 20390 (F-28, 29)
GIST, LEWIS A., Ph.D., Science Manpower
Improvement, National Science Foundation,
Washington, D.C. 20550 (F)
GIWER, MATTHIAS M., 3922 Millcreek Dr.,
Annandale, Va. 22003 (M)
GLADSTONE, VIC S., Ph.D., 8200 Andes Ct.,
Baltimore, Md. 21208 (M-6, 25)
GLASGOW, Augustus R., Jr., Ph.D., 4116 Hamil-
ton St., Hyattsville, Md. 20781 (F-4, 6)
GLAZEBROOK, THOMAS B., 7809 Bristow Dr.,
Annandale, Va. 22003 (F-11)
GLICKSMAN, MARTIN E., Ph.D., 8 Via Maria,
Scotia, N.Y. 12302 (F-20, 36)
104
GLUCKSTERN, ROBERT L., Ph.D., Chancellor
Univ. of Md., College Park, Md. 20742 (F-31)
GODFREY, THEODORE B., 7508 Old Chester
Rd., Bethesda, Md. 20034 (E)
GOFF, JAMES F., Ph.D., 3405 34th Pl., N.W.,
Washington, D.C. 20016 (F-1)
GOLDBERG, MICHAEL, 5823 Potomac Ave.,
N.W., Washington, D.C. 20016 (F-1, 38)
GOLDBERG, ROBERT N., Ph.D., 19610 Brassie
P!., Gaithersburg, Md. 20760 (F-39)
GOLDMAN, ALAN J., Ph.D., Applied Math. Div.
Inst. for Basic Standards, Natl. Bureau of
Standards, Washington, D.C. 20234 (F-34, 38)
GOLDSMITH, HERBERT, 238 Congressional
Lane, Rockville, Md. 20852 (M-32, 35)
GOLUMBIC, CALVIN, 6000 Highboro Dr.,
Bethesda, Md. 20034 (F)
GONET, FRANK, 4007 N. Woodstock St., Arling-
ton, Va. 22207 (F-4, 39)
GOODE, ROBERT J., B.S., Strength of Metals
Br., Code 6380, Metallurgy Div., U.S.N.R.L.,
Washington, D.C 20390 (F-6, 20)
GORDH, GORDON, Systematic Entomology Lab.
11B111, U.S. National Museum, Washington,
D.C. (M)
GORDON, CHARLES L., 5512 Charles St.,
Bethesda, Md. 20014 (E-1, 4, 6)
GORDON RUTH E., Ph.D., Waksman Inst. of
Microbiology, Rutgers Univer., P.O. Box
759, Piscataway, N.J. 08854 (F-16)
GRAHN, Mrs. ANN, M.A., 849 So. La Grange Rd.,
La Grange, Ill. 60525 (M)
GRAMANN, RICHARD H., 1613 Rosemont CT,
McLean, Va. 22101 (M)
GRAY, ALFRED, Dept. Math., Univ. of Maryland,
College Park, Md. 20742 (F)
GRAY, IRVING, Ph.D., Georgetown Univ., Wash-
ington, D.C. 20007 (F-19)
GREENOUGH, M. L., M.S., Greenough Data
Assoc., 616 Aster Blvd., Rockville, Md. 20850
(F)
GREENSPAN, MARTIN, B.S., 12 Granville Dr.,
Silver Spring, Md. 20902 (F-1, 25)
GRISAMORE, NELSON T., Nat. Acad. Sci., 2101
Constitution Ave., N.W., Washington, D.C.
20418 (F)
GRISCOM, DAVID L., Ph.D., Material Sci. Div.,
Naval Res. Lab., Washington, D.C. 20375
(F-6, 28)
GROSSLING, BERNARDO F., Rm. 4B102, USGS
Nat. Ctr., 12201 Sunrise Valley Dr., Reston,
Va. 22092 (F-7)
GURNEY, ASHLEY B., Ph.D., Systematic Ento-
mology Laboratory, USDA, % U.S. National
Museum, NHB-105, Washington, D.C. 20560
(F-3, 5, 6)
GUTTMAN, CHARLES M., 9510 Fern Hollow Way,
Gaithersburg, Md. 20760 (F)
H
HACSKAYLO, EDWARD, Ph.D., Agr. Res. Ctr.,
West, Beltsville, Md. 20705 (F-6, 10, 11, 33)
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
HAENNI, EDWARD O., Ph.D., 7907 Glenbrook
Rd., Bethesda, Md. 20014 (F-4, 39)
HAGAN, LUCY B., Ph.D., Natl. Bur. Stds., Rm.
A155, Bg. 221, Washington, D.C. 20234 (M-4,
32)
HAINES, KENNETH A., M.S., ARS, 3542 N. Dela-
ware St., Arlington, Va. 22207 (F-5, 24)
HALL, E. RAYMOND, Ph.D., Museum of Natural
History, Univ. of Kansas, Lawrence, Kans.
66044 (E-3, 6)
HALL, R. CLIFFORD, M.F., 316 Mansion Drive,
Alexandria, Va. 22302 (E-11)
HALL, STANLEY A., M.S., 9109 No. Branch Dr.,
Bethesda, Md. 20034 (F-4, 24)
HALL, WAYNE C., Ph.D., 557 Lindley Dr.,
Lawrence, Kans. 66044 (E-6, 13)
HALLER, WOLFGANG, Ph.D., National Bureau
of Standards, Washington, D.C. 20234 (F)
HAMBLETON, EDSON J., 5140 Worthington Dr.,
Washington, D.C. 20016 (E-3, 5, 6)
HAMER, WALTER J., Ph.D., 3028 Dogwood St.,
N.W., Washington, D.C. 20015 (F-4, 13, 29, 39)
HAMMER, GUYS, II, 8902 Ewing Dr., Bethesda,
Md. 20034 (M-12, 13)
HAMMOND, DAVID H., 14 Chappel St., Brock-
port, N.Y. 14420 (M-10)
HAMPP, EDWARD G., D.D.S., National Institutes
of Health, Bethesda, Md. 20014 (F-21)
HAND, CADET H., Jr., Bodega Marine Lab.,
Bodega Bay, Calif. 94923 (F-6)
HANSEN, LOUIS S., D.D.S., School of Dentistry,
San Francisco, Med. Center, Univ. of Calif.,
San Francisco, Calif. 94122 (F-21)
HANSEN, MORRIS, H., M.A., Westat Research,
Inc., 11600 Nebel St., Rockville, Md. 20852
(F)
HARDENBURG, ROBERT E., Ph.D., Agr. Mktg.
Inst., Agr. Res. Ctr (W), Beltsville, Md. 20705
(F-6)
HARR, JAMES W., M.A., 9503 Nordic Dr.,
Lanham, Md. 20801 (M-6)
HARRINGTON, FRANCIS D., Ph.D., 4600 Ocean
Beach Blvd., #204, Cocoa Beach, Fla.
32931 (F)
HARRINGTON, M. C., Ph.D., 4545 Connecticut
Ave., N.W., Apt. 334, Washington, D.C. 20008
(E-1,/22; 31, 32)
HARRIS, MILTON, Ph.D., 3300 Whitehaven St.,
N.W., Suite 500, Washington, D.C. 20007 (F)
HARRISON, W. N., 3734 Windom PI., N.W.,
Washington, D.C. 20016 (F-1, 6, 25)
HARTLEY, JANET W., Ph.D., National Inst. of
Allergy & Infectious Diseases, National In-
stitutes of Health, Bethesda, Md. 20014 (F)
HARTMANN, GREGORY K., Ph.D.,10701 Keswick
St., Garrett Park, Md. 20766 (F-1, 25)
HARTZLER, MARY P., 3326 Hartwell Ct., Falls
Church, Va. 22042 (M-6)
HASKINS, C. P., Ph.D., 2100 M St., N.W., Suite
600 Washington. D.C. 20037 (F)
HAS, GEORG H., 7728 Lee Avenue, Alexandria,
Va. 22308 (F-32)
HAUPTMAN, HERBERT, Ph.D., Med. Fndn. of
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
Buffalo, 73 High St., Buffalo, N.Y. 14203
(F-1, 6, 38)
HAYDEN, GEORGE A., 1312 Juniper St. N.W.,
Washington, D.C. 20012 (M)
HAYES, PATRICK, Ph.D., 950 25th St., Apt. 707,
Washington, D.C. 20037 (F)
HEADLEY, ANNE R., Ph.D., Ms., 2500 Virginia
Ave., N.W., Washington, D.C. 20037 (F)
HEANEY, JAMES B., 6 Olivewood Ct., Greenbelt,
Md. 20770 (F)
HEIFFER, M. H., Whitehall, #701, 4977 Battery
La., Bethesda, Md. 20014 (F-6, 19)
HEINRICH, KURT F., 804 Blossom Dr., Woodley
Gardens, Rockville, Md. 20850 (F)
HEINS, CONRAD P., Ph.D., 4919 Powder Mill
Rd., Beltsville, Md. 20742 (F-6, 18)
HENDERSON, E. P., Div. of Meteorites, U.S. Na-
tional Museum, Washington, D.C. 20560 (E-7)
HENDRICKSON, WAYNE A., M.D., Ph.D., Lab. for
the Structure of Matter, Naval Res. Lab.
Code 6030, Washington, D.C. 20375 (F)
HENNEBERRY, THOMAS J., 1409 E. North
Share, Temple, Ariz. 85282 (F)
HENRY, WARREN E., Ph.D., Howard Univ.,
P.O. Box 761, Washington, D.C. 20059 (F)
HENVIS, BERTHA W., Code 5277, Naval Res.
Lab., Washington, D.C. 20375 (M)
HERBERMAN, RONALD B., 8528 Atwell Rd.,
Potomac, Md. 20854 (F)
HERMACH, FRANCIS L., 2415 Eccleston St.,
Silver Spring, Md. 20902 (F-1, 6, 13, 25)
HERMAN, ROBERT, Ph.D., Traffic Sci. Dept.,
General Motors Res. Lab., 12 Mi & Mound
Rds., Warren, Mich. 48090 (F-1)
HERSCHMAN, HARRY K., 4701 Willard Ave.,
Chevy Chase, Md. 20015 (E)
HERSEY, JOHN B., 923 Harriman St., Great Falls,
Va. 22066 (M-25)
HERSEY, MAYO D., M.A., Div. of Engineering,
Brown Univ., Providence, R.I. 02912 (E-1)
HERZFELD, KARL F., Dept. of Physics, Catholic
Univ., Washington, D.C. 20017 (E-1)
HESS, WALTER, C., 3607 Chesapeake St., N.W.,
Washington, D.C. 20008 (E-4, 6, 19, 21)
HEWSTON, ELIZABETH, Felicity Cove, Shady
Side, Md. 20867 (F-39)
HEYDEN, FR. FRANCIS, Ph.D., Manila Observa-
tory, P.O. Box 1231, Manila, Philippines D-404
(E-32)
HEYER, W. R., Ph.D., Amphibians & Reptiles,
Natural History Bldg., Smithsonian Inst.,
Washington, D.C. 20560 (F-3)
HIATT, CASPAR W., Ph.D., Univ. of Texas Health
Science Center, 7703 Floyd Curl Dr., San
Antonio, Texas 78284 (F)
HICKLEY, THOMAS J., 626 Binnacle Dr., Naples,
Fla. 33940 (F-13)
HICKOX, GEORGE H., Ph.D., 9310 Allwood Ct.,
Alexandria, Va. 22309 (E-6, 14, 18)
HILDEBRAND, EARL M., 11092 Timberline Dr.,
Sun City, Ariz. 85351 (E-10, 16, 27, 42)
HILL, FREEMAN K., Ph.D., 12408 Hall’s Shop Rd.,
Fulton, Md. 20759 (F-1, 6, 22)
HILLABRANT, WALTER, Ph.D., Dept. Psychol-
105
ogy, Howard Univ., Washington, D.C. 20059
(M-40)
HILSENRATH, JOSEPH, 9603 Bruneit Ave., Silver
Spring, Md. 20901 (F-1, 38)
HILTON, JAMES L., Ph.D., Agr. Res. Ctr. (W),
USDA, ARS, Beltsville, Md. 20705 (F-33)
HOBBS, ROBERT B., 7715 Old Chester Rd.,
Bethesda, Md. 20034 (F-1, 4, 39)
HOFFMANN, C. H., Ph.D., 6906 40th Ave., Univer-
sity Park, Hyattsville, Md. 20782 (E-5, 11, 24)
HOGE, HAROLD J., Ph.D., 5 Rice Spring Lane,
Wayland, Me. 01778 (F-1)
HOLLIES, NORMAN R. S., Gillette Research
Institute, 1413 Research Blvd., Rockville, Md.
20850 (F-4)
HOLMGREN, HARRY D., Ph.D., 3044-3 R St.,
N.W., Washington, D.C. 20007 (F-1)
HOLSHOUSER, WILLIAM L., 513 N. Oxford St.,
Arlington, Va. 22203 (F-6, 20)
HONIG, JOHN G., Office, Dep. Chief of Staff
for Res., Dev. and Acquis., Army, The Penta-
gon, Washington, D.C. 20310 (F-34)
HOOD, KENNETH J., 2000 Huntington Ave.,
#1118, Alexandria, Va. 22303 (M-6, 33)
HOOVER, JOHN |., B.A., 5313 Briley Place, Wash-
ington, D.C. 20016 (F-1)
HOPP, HENRY, Ph.D., 7604 Winterberry Place,
Bethesda, Md. 20034 (F-11)
HOPPS, HOPE E., Mrs., 1762 Overlook Dr., Silver
Spring, Md. 20903 (F-19)
HORNSTEIN, IRWIN, Ph.D., 5920 Bryn Mawr Rad.,
College Park, Md. 20740 (F-4, 27)
HOROWITZ, E., Asst. Deputy Director, Institute
for Materials Res., National Bureau of Stand-
ards, Washington, D.C. 20234 (F)
HORTON, BILLY M., 14250 Larchmere Blvd.,
Shaker Heights, Ohio 44120 (F-1, 6, 13)
HOWARD, JAMES H., Ph.D., 3822 Albemarle St.,
N.W., Washington, D.C. 20016 (F)
HUANG, KUN-YEN, M.D., Ph.D., 1445 Laurel
Hill Rd., Vienna, Va. 22180 (F-16)
HUBBARD, DONALD, PH.D., 4807 Chevy Chase
Dr., Chevy Chase, Md. 20015 (F-4, 6, 32)
HUBERT, LESTER F., 4704 Mangum Rad., College
Park, Md. 20740 (F-23)
HUDSON, COLIN M., Ph.D., Product Planning
Dept., Deere & Co., John Deere Rd., Mocine,
Il. 61265 (F-6, 17, 22)
HUDSON, GEORGE E., Code WR 4, Naval Surface
Weapons Ctr., White Oak, Silver Spring, Md.
20910 (F-1, 6)
HUDSON, RALPH P., Ph.D., National Bureau of
Standards, Washington, D.C. 20234 (F-1)
HUGH, RUDOLPH, Ph.D., George Washington
Univ. Sch. of Med., Dept. of Microbiology,
2300 Eye St. N.W., Washington, D.C. 20037
(F-16, 19)
HUNT, W. HAWARD, B.A., 11712 Roby Ave.,
Beltsville, Md. 20705 (M-6)
HUNTER, RICHARD S., 9529 Lee Highway,
Fairfax, Va. 22030 (F-6, 27, 32)
HUNTER, WILLIAM R., M.S., Code 7143, U.S.
Naval Research Lab., Washington, D.C. 20375
(F-1, 6, 32)
106
HURDLE, BURTON G., 6222 Berkeley Rd., Alex-
andria, Va. 22307 (F-25)
HURTT, WOODLAND, Ph.D., ARS-USDA, P.O.
Box 1209, Frederick, Md. 21701 (M-33)
HUTCHINS, LEE M., Ph.D., Apartado 5202, San
Jose, Costa Rica (E-6, 10, 11)
HUTTON, GEORGE L., 809 Avondale Dr., W.
Lafayette, Ind. 47906 (F)
INSLEY, HERBERT, Ph.D., 5 Ground Place,
Albany, N.Y. 12205 (E-1, 7)
IRVING, GEORGE W., Jr., Ph.D., 4836 Langdrum
Lane, Chevy Chase, Md. 20015 (F-4, 27, 39)
IRWIN, GEORGE R., Ph.D., 7306 Edmonston Rad.,
College Park, Md. 20740 (F-1, 6)
ISBELL, H. S., 4704 Blagden Ave.,
Washington, D.C. 20011 (F-4)
ISENSTEIN, Robert S., Animal Parasitology Inst.
Barc-East, USDA, Beltsville, Md. 20705 (M)
N.W.,
J
JACKSON, H. H. T., Ph.D., 122 Pinecrest Rd.,
Durham, N.C. (E-3)
JACKSON, PATRICIA C., Ms., Rm. 207, Bg. 001,
Agr. Res. Ctr. (W), ARS, USDA, Beltsville,
Md. 20705 (M-4, 6, 33)
JACOBS, WOODROW C., Ph.D., 6309 Bradley
Bivd., Bethesda, Md. 20034 (F-23)
JACOBSON, MARTIN, U.S. Dept. of Agriculture,
Agr. Res. Center (E) Beltsville, Md. 20705
(F-4, 7, 24)
JACOX, MARILYN E., Ph.D., National Bureau of
Standards, Washington, D.C. 20234 (F-4)
JAFFE, LOUIS S., M.A., 1001 Highland Dr.,
Silver Spring, Md. 20910 (F-4)
JAMES, MAURICE T., Ph.D., Dept. of Ento-
mology, Washington State University, Pull-
man, Washington 99163 (E-5)
JANI, LORRAINE L., P.O. Box 898, Lutz, FI.
33549 (M)
JAROSEWICH, EUGENE, NMNH, Smithsonian
Inst., Washington, D.C. 20560 (M-4, 6)
JEN, C. K., Applied Physics Lab., John Hopkins
Rd., Laurel, Md. 20810 (E)
JENSON, ARTHUR S., Ph.D., Westinghouse
Defense & Electronic Systems Ctr., Box 1521,
Baltimore, Md. 21203 (F-13, 31, 32)
JESSUP, R. S., 7001 W. Greenvale Pkwy., Chevy
Chase, Md. 20015 (F-1, 6)
JOHANNESEN, ROLF B., Ph.D., National Bureau
of Standards, Washington, D.C. 20234 (F-4, 6)
JOHNSON, CHARLES, Ph.D., Inst. for Fluid Dy-
namics & App. Math. Univ. of Md., College
Park, Md. 20850 (F)
JOHNSON, DANIEL P., Ph.D., Rt. 1, Box 156,
Bonita, La. 71223 (E-1, 35)
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
JOHNSON, KEITH C., 4422 Davenport St., N.W.,
Washington, D.C. 20016 (F)
JOHNSON, PHILLIS T., Ph.D., Nat. Marine
Fisheries Serv., Oxford Lab., Oxford, Md.
21654 (F-5, 6)
JOHNSTON, FRANCIS E., Ph.D., 307 W. Mont-
gomery Ave., Rockville, Md. 20850 (E-1)
JONES, HENRY A., 1115 South 7th St., El Centro,
Calif. 92243 (E)
JONES, HOWARD S., 6200 Sligo Mill Rd., N.E.,
Washington, D.C. 20011 (F-6, 13)
JONG, SHUNG-CHANG, Ph.D., Amer. Type Cul-
ture Collection, 12301 Parkland Dr., Rock-
ville, Md. 20852 (F)
JORDAN, GARY BLAKE, 1012 Olmo Ct., San
Jose, Calif. 95129 (M-6, 13)
JUDD, NEIL M., % C. A. McCary, 5311 Acacia
Ave., Bethesda, Md. 20014 (E-2, 6)
K
KABLER, MILTON N., Ph.D., 3109 Cunningham
Dr., Alexandria, Va. 22309 (F)
KAISER, HANS E., 433 South West Dr., Silver
Spring, Md. 20901 (M-6)
KARLE, ISABELLA, Code 6030, U.S. Naval Res.
Lab., Washington, D.C. 20375 (F-4, 6)
KARLE, JEROME, Code 6030, U.S. Naval Re-
search Lab., Washington, D.C. 20375
(F-1, 4)
KARR, PHILIP R., 5507 Calle de Arboles, Tor-
rance, Calif. 90505 (F-13)
KARRER, ANNIE M. H., Ph.D., Port Republic,
Md. 20676 (E-6) ;
KAUFMAN, H. P., M.P.L., Box 1135, Fedhaven,
Fla. 33854 (F-12)
KEARNEY, PHILIP C., Ph.D., 13021 Blairmore St.,
Beltsville, Md. 20705 (F-4)
KEGELES, GERSON, RFD 2, Stafford Springs,
Conn. 06076 (F)
KENNARD, RALPH B., Ph.D., Apt., 1207 Ross-
moor Tower |, Leisure World, Laguna Hills,
Calif. 92653 (E-1, 6, 31, 32)
KESSLER, KARL G., Ph.D., Optical Physics Div.,
Natl. Bureau of Standards, Washington, D.C.
20234 (F-1, 6, 32)
KEULEGAN, GARBIS H., Ph.D., 215 Buena Vista
Dr., Vicksburg, Miss. 39180 (F-1, 6)
KLEBANOFF, PHILIP S., Fluid Dynamics Sect.,
National Bureau of Standards, Washington,
D.C. 20234 (F-1, 22)
KLINGSBERG, CYRUS, % Solar, 624 Arbor Rd.,
Cheltenham, Pa. 19012 (F-26, 28)
KLUTE, CHARLES H., Ph.D., Apt. 118, 4545 Con-
necticut Ave., N.W., Washington, D.C. 20008
(F-1, 4, 39).
KNOBLOCK, EDWARD C., RD 4, Box 332;
Mt. Airy, Md. 21771 (F-4, 19)
KNOWLTON, KATHRYN, Ph.D., Apt. 837, 2122
Massachusetts Ave., N.W., Washington, D.C.
20008 (F-4, 19)
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
KNOX, ARTHUR S., M.A., M.Ed., 2006 Columbia
Rd., N.W., Washington, D.C. 20009 (M-6, 7)
KNUTSON, LLOYD V., Ph.D., Insect Introduction
Inst., USDA, Beltsville, Md. 20705 (F-5)
KRUGER, JEROME, Ph.D., Rm B254, Materials
Bldg., Natl. Bur. of Standards, Washington,
D.C. 20234 (F-4, 29, 36)
KURTZ, FLOYD E., 8005 Custer Rd., Bethesda,
Md. 20014 (E-4)
KUSHNER, LAWRENCE M., Ph.D., Commis-
sioner, Consumer Product Safety Commis-
sion, Washington, D.C. 20207 (F)
5
LABENZ, PAUL J., P.O. Box 30198, Bethesda,
Md. 20014
LADO, ROBERT, Ph.D., Georgetown Univ., Wash-
ington, D.C. 20007 (F)
LAKI, KOLOMAN, Ph.D., Bldg. 4, Natl. Inst. of
Health, Bethesda, Md. 20014 (F)
LANDSBERG, H. E., 5116 Yorkville Rd., Temple
Hills, Md. 20031 (F-1, 23)
LANG, MARTHA E. C., B.S., Connecticut Ave.,
N.W., Washington, D.C. 20008 (F-6, 7)
LANGFORD, GEORGE S., Ph.D., 4606 Hartwick
Rd., College Park, Md. 20740 (E-5, 24)
LAPHAM, EVAN G., 2242 S.E. 28th St., Cape
Coral, Fla. 33904 (E)
LARMORE, LEWIS, Off. of Naval Res., 800 N.
Quincey St., Arlington, Va. 22217 (M-6, 32)
LASHOF, THEODORE W., 10125 Ashburton
Lane, Bethesda, Md. 20034 (F)
LASTER, HOWARD J., Ph.D., Dean, College of
Liberal Arts, Univ. of lowa, lowa City,
lowa 52242 (F-1, 31)
LAWSON, ROGER H., 4912 Ridge View Lane,
Bowie, Md. 20715 (F-6, 42)
LEACHMAN, ROBERT B., Ph.D., 5315 Wapako-
neta Rd., Bethesda, Md. 20016 (F-1, 26)
LE CLERG, ERWIN L., 14620 Deerhurst Terrace,
Silver Spring, Md. 20906 (E-10, 42)
LEE, RICHARD H., RD 2, Box 143E, Lewes, Del.
19958 (E)
LEIBOWITZ, JACK R., 12608 Davan Dr., Silver
Spring, Md. 20904 (F)
LEINER, ALAN L., 580 Arastradero Rd., #804,
Palo Alto, Calif. 94306 (F)
LEJINS, PETER P., Univ. of Maryland, Inst.
Crim. Justice and Criminology, College Park,
Md. 20742 (F-10)
LENTZ, PAUL LEWIS, Ph.D., 5 Orange Ct.,
Greenbelt, Md. 20770 (F-6, 10)
LESSOFF, HOWARD, Code 5220, Naval Res. Lab..,
Washington, D.C. 20375 (F)
LEVY, SAMUEL, 2279 Preisman Dr., Schenec-
tady, N.Y. 12309 (F)
LIDDEL, URNER, 2939 Van Ness St. N.W., Apt.
1135, Washington, D.C. 20008 (E-1)
LIEBLEIN, JULIUS, 1621 E. Jefferson St., Rock-
ville, Md. 20852 (F-34)
107
LIN, MING CHANG, Ph.D., 9513 Fort Foote Rd.,
Oxon Hill, Md. 20022 (F-4, 32)
LINDQUIST, A. W., Rt. 1, Box 36, Lindsberg,
Kansas 67456 (E)
LINDSEY, IRVING, M.A., 202 E. Alexandria Ave.,
Alexandria, Va. 22301 (E)
LING, LEE, 1608 Belvoir Dr., Los Altos, Calif.
94022 (E)
LINK, CONRAD B., Dept. of Horticulture, Univ.
of Maryland, College Park, Md. 20742 (F-6,
10)
LINNENBOM, VICTOR J., Ph.D., Code 8300,
Naval Res. Lab., Washington, D.C. 20390
(G4) |
LIST, ROBERT J., 1123 Hammond Pkwy., Alex-
andria, Va. 22302 (F-23)
LITTLE, “ELBERT -L Jr;. Ph:b., 924. 20th St:
S. Arlington, Va. 22202 (F-10, 11)
LOCKARD, J. DAVID, Ph.D., Botany Dept., Univ.
of Maryland, College Park, Md. 20742 (F-33)
LOEBENSTEIN, WILLIAM V., Ph.D., 8501 Sun-
dale Dr., Silver Spring, Md. 20910 (F-4, 21)
LONG, B. J. B., Mrs., 416 Riverbend Rd., Oxon
Hill, Md. 20022 (M)
LORING, BLAKE M., Sc.D., Rt. 2, Laconia, N.H.
03246 (F-6, 20, 36)
LUSTIG, ERNEST, Ph.D., Ges Biotechnol Forsch
Mascheroder Weg 1, 3300 Braunschweig 66,
W. Germany (F-4)
LYNCH, Mrs. THOMAS J., 1062 Harriman St.,
Great Falls, Va. 22066 (M)
LYONS, JOHN W., Rte. 4, Box 261, Mount Airy,
Md. 21771 (F-4)
MA, TE-HSIU, Dept. of Biological Science, West-
ern Illinois Univ., Macomb, Ill. 61455 (F-10, 19)
MADDEN, ROBERT P., A251 Physics Bldg., Natl.
Bureau of Standards, Washington, D.C.
20234 (F-32)
MAENGWYN-DAVIES, G. D., Ph.D., 15205 Totten-
ham Terr., Silver Spring, Md. 20206 (F-6, 19)
MAGIN, GEORGE B., Jr., 7412 Ridgewood Ave.,
Chevy Chase, Md. 20015 (F-6, 7, 26)
MAHAN, A. I., Ph.D., 10 Millgrove Place, Ednor,
Md. 20904 (E-1, 32)
MAIENTHAL, MILLARD, 10116 Bevern Lane,
Potomac, Md. 20854 (F-4)
MANDEL, JOHN, Ph.D., B356 Chem. Bg., Natl.
Bur. of Standards, Washington, D.C. 20234
(F-1)
MANDERSCHEID, RONALD W., Ph.D., 202
Montgomery Ave., 1, Rockville, Md. 20854
(F-43)
MANGUS, JOHN D., 6019 Berwyn Rd., College
Park, Md. 20740 (F)
MANNING, JOHN R., Ph.D., Metallurgy Div.,
Natl. Bur. of Standards, Washington, D.C.
20234 (F-20)
MARCHELLO, JOSEPH M., Ph.D., 3624 Marl-
borough Way, College Park, Md. 20742 (F)
108
MARCUS, MARVIN, Ph.D., Dept. Math., Univ. of .
California, Santa Barbara, Calif. 93106
(F-6, 38)
MARGOSHES, MARVIN, Ph.D., 69 Midland Ave.,
Tarrytown, N.Y. 10591 (F)
MARTIN, BRUCE D., P.O. Box 234, Leonardtown,
Md. 20650 (E-7)
MARTIN, JOHN H., Ph.D., 124 N.W. 7th St., Apt.
303, Corvallis, Oregon 97330 (E-6)
MARTIN, ROBERT H., 2257 N. Nottingham St.,
Arlington, Va. 22205 (M-23)
MARTON, L., Ph.D., Editorial Office, 4515 Lin-
nean Ave., N.W., Washington, D.C. 20008 (E-
113, 31)
MARVIN, ROBERT S., 11700 Stony Creek Rd.,
Potomac, Md. 20854 (E-1, 4, 6)
MARYOTT, ARTHUR A., 4404 Maple Ave.,
Bethesda, Md. 20014 (E)
MASON, HENRY LEA, Sc.D., 7008 Meadow Lane,
Chevy Chase, Md. 20015 (F-6, 14, 35)
MASSEY, JOE T., Ph.D., 10111 Parkwood Dr.,
Bethesda, Md. 20014 (F-1, 13)
MATLACK, MARION, Ph.D., 2700 N. 25th St.,
Arlington, Va. 22207 (E-4, 6)
MAUSS, BESSE D., Rural Rt. 1, New Oxford, Pa.
17350 (F) :
MAXWELL, LOUIS R., Ph.D., 3506 Leland St.,
Chevy Chase, Md. 20015 (F-1)
MAY, DONALD C., Jr., Ph.D., 5931 Oakdale Rd.,
McLean, Va. 22101 (F)
MAY, IRVING, M.S., U.S. Geological Survey,
National Ctr. 912, Reston, Va. 22092 (F-4, 6, 7)
MAYOR, JOHN R., Asst. Provost for Res.,
1120H, Univ. Maryland, College Park, Md.
Univ. Maryland, College Park, Md. 20742 (F)
MC BRIDE, GORDON W., Ch.E., 3323 Stuyvesant
Pl. N.W., Chevy Chase, D.C. 20015 (E-4)
MC CAMY, CALVIN S., M.S., 54 All Angels Hill
Rd., Wappingers Falls, N.Y. 12590 (F-32)
MC CULLOUGH, JAMES M., Ph.D., 6209 Apache
St., Springfield, Va. 22150 (M)
MC CULLOUGH, N. B., Ph.D., M.D., Dept. of
Microbiology & Public Health, Michigan State
Univ., East Lansing, Mich. 48823 (F-6, 8)
MC ELHINNEY, JOHN, Ph.D., 11601 Stephen Rad.,
Silver Spring, Md. 20904 (F-1, 13, 26)
MC GUNIGAL, THOMAS E., J.D., 13613 Highland
Rd., Clarksville, Md. 21029 (F-1, 13)
MC INTOSH, ALLEN, 4606 Clemson Rad., College
Park, Md. 20740 (E-6, 15)
MC KELVEY, VINCENT E., Ph.D., 6601 Broxburn
Dr., Bethesda, Md. 20034 (F-7)
MC KENZIE, LAWSON W., A.M., 5311 West
Pathway, Washington, D.C. 20016 (F-1)
MC NESBY, JAMES R., Dept. of Chemistry,
Univ. of Md., College Park, Md. 20742 (F-1, 4)
MC PHEE, HUGH C., 3450 Toledo Terrace, Apt.
425, Hyattsville, Md. 20782 (E-6) i
MC PHERSON, ARCHIBALD T., Ph.D., 403
Russell Ave., Apt. 804, Gaithersburg, Md.
20760 (L-1, 4, 6, 27)
MC WRIGHT, CORNELIUS G., 7409 Estaban PI.,
Springfield, Va. 22151 (M)
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
MEADE, BUFORD K., 5516 Bradley Blvd., Alex-
andria, Va. 22311 (F-17)
MEARS, FLORENCE, M., Ph.D., 8004 Hampden
Lane, Bethesda, Md. 20014 (E)
MEARS, THOMAS W., B.S., 2809 Hathaway Ter-
race, Wheaton, Md. 20906 (F-1, 4, 6)
MEBS, RUSSELL W., Ph.D., 6620 32nd St., N.,
Arlington, Va. 22213 (F-12, 20)
MELMED, ALLAN J., 732 Tiffany Court, Gaithers-
burg, Md. 20760 (F)
MENDELSOHN, MARK B., Psychology Dept.,
George Mason Univ., 4400 University Dr.,
Fairfax Va. 22030 (F-40)
MENIS, OSCAR, Analytical Chem. Div., Natl.
Bureau of Standards, Washington, D.C.
20234 (F)
MENZER, ROBERT E., Ph.D., 7203 Wells Pkwy.,
Hyattsville, Md. 20782 (F-4, 24)
MERRIAM, CARROLL F., Prospect Harbor,
Maine 04669 (F-6) -
MESSINA, CARLA G., M.S., 9916 Montauk Ave.,
Bethesda, Md. 20034 (F)
MEYERHOFF, HOWARD A., Ph.D., 3625 S. Flor-
ence PI., Tulsa, Okla. 74105 (F-6, 7)
MEYERSON, MELVIN R., Ph.D., A347, Polymer
Bg., National Bureau of Standards, Wash-
ington, D.C. 20234 (F-20)
MICHAELIS, ROBERT E., National Bureau of
Standards, Chemistry Bldg., Rm. B314,
Washington, D.C. 20234 (F-20)
MIDDLETON, H. E., Ph.D., 302 Maple Ave.,
Richmond, Va. 23226 (E)
MILLAR, DAVID B., NMRI, NNMC, Stop 36,
Physical Biochemistry Div., Washington,
D.C. 20014 (F)
MILLER, CARL F., M.A., P.O..Box 127, Gretna, Va.
24557 (E-2, 7)
MILLER, CLEM O., Ph.D., 6343 Nicholson St.,
Falls Church, Va. 22044 (F-4, 6, 39)
MILLER, J. CHARLES, Ph.D., 10600 Eastborne
Ave., Apt. 7, W. Los Angeles, California 90024
(E-7, 36)
MILLER, PAUL R., Ph.D., 207 S. Pebble Beach
Blvd., Sun City Ctr., Fla. 33570 (E-10, 42)
MILLER, RALPH L., Ph.D., 5215 Abington Rd.,
Washington, D.C. 20016 (F-7)
MILLER, W. ROBERT, Mrs., 11632 Deborah Dr.,
Potomac, Md. 20854 (F-6)
MILLER, ROMAN R., 1232 Pinecrest Circle, Silver
Spring, Md. 20910 (F-4, 6, 28)
MILLIKEN, LEWIS T., SSL Res. Inst. 43-20,
NHTSA, 400 7th St., S.W., Washington, D.C.
20590 (M-1, 4, 6, 7)
MITCHELL, J. MURRAY, Jr., Ph.D., 1106 Dog-
wood Dr., McLean, Va. 22101 (F-6, 23)
MITCHELL, JOHN W., 9007 Flower Ave., Silver
Spring, Md. 20901 (F)
MITTLEMAN, DON, Ph.D., 80 Parkwood Lane,
Oberlin, Ohio 44074 (F-1)
MIZELL, LOUIS R., 108 Sharon Lane, Greenlawn,
N.Y. 11740 (F)
MOLINO, JOHN A., Ph.D., Sound Bldg., Nat.
Bureau Standards, Washington, D.C. 20234
(M-25)
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
MOLLARI, MARIO, 4527 45th St., N.W., Washing-
ton, D.C. 20016 (E-3, 5, 15)
MOORE, GEORGE A., Ph.D., Natl. Bur. of Stand-
ards 312.03, Washington, D.C. 20234 (F-6,
20, 29, 36)
MORRIS, J. A., 23-E Ridge Rd., Greenbelt, Md.
20770 (M-6, 15, 16)
MORRIS, JOSEPH BURTON, Ph.D., Chemistry
Dept. Howard Univ., Washington, D.C. 20059
(F-4)
MORRIS, KELSO B., Howard Univ., Washington,
D.C. 20059 (F-4, 39)
MORRISS, DONALD J., 102 Baldwin Ct., Pt. Char-
lotte, Fla. 33950 (E-11)
MOSTOFI, F. K., M.D., Armed Forces Inst. of
Pathology, Washington, D.C. 20306 (F)
MOUNTAIN, RAYMOND D., B216 Physics Bg.,
Nat. Bureau of Standards, Washington, D.C.
20234 (F)
MUEHLHAUSE, C. O., Ph.D., 9105 Seven Locks
Rd., Bethesda, Md. 20034 (F-1, 26)
MUELLER, H. J., 4801 Kenmore Ave., Alexandria,
Va. 22304 (F)
MUESEBECK, CARL F. W., U.S. Natl. Museum
of Nat. Hist., Washington, D.C. 20560 (E-3, 5)
MULLIGAN, JAMES H., Ph.D., 12121 Sky Lane,
Santa Ana, Calif. 92705 (F-12, 13, 38)
MURDOCH, WALLACE P., Ph.D., Rt. 2, Gettys-
burg, Pa. 17325 (F-5, 6, 24)
MURRAY, THOMAS H., 2915 27th St., N. Arling-
ton, Va. 22207 (M)
MURRAY, WILLIAM S., Ph.D., 1281 Bartonshire
Way, Potomac Woods, Rockville, Md. 20854
(F-5)
MYERS, RALPH D., Physics Dept., Univ. of Mary-
land, College Park, Md. 20740 (F-1)
N
NAESER, CHARLES R., Ph.D., 6654 Van Winkle
Dr., Falls Church, Va. 22044 (F-4, 7, 39)
NAMIAS, JEROME, Sc.D., 2251 Sverdrup Hall,
Scripps Institution of Oceanography, La
Jolla, Calif. 92037 (F-23)
NELSON, R. H., 7309 Finns Lane, Lanham, Md.
20801 (E-5, 6, 24)
NEPOMUCENE, SR. ST. JOHN, Villa Julie, Valley
Rd., Stevenson, Md. 21153 (E-4) .
NEUENDORFFER, J. A., 911 Allison St., Alex-
andria, Va. 22302 (F-6, 34)
NEUSCHEL, SHERMAN K., 7501 Democracy
Blvd., Bethesda, Md. 20034 (F-7)
NEWMAN, MORRIS, Dept. of Mathematics, Univ.
of Calif., Santa Barbara, Calif. 93106 (F)
NICKERSON, DOROTHY, 4800 Fillmore Ave., Apt.
450, Alexandria, Va. 22311 (E-6, 32)
NIKIFOROFF, C. C., 4309 Van Buren St., Univer-
sity Park, Hyattsville, Md. 20782 (E)
NOFFSINGER, TERRELL L., 9623 Sutherland
Rd., Silver Spring, Md. 20901 (F-6, 23)
NORRIS, KARL H., 11204 Montgomery Rad.,
Beltsville, Md. 20705 (F-27)
109
NOYES, HOWARD E., Ph.D., 4807 Aspen Hill
Rd., Rockville, Md. 20853 (F-16, 19)
O
O’BRIEN, JOHN A., Ph.D., Dept. of Biology,
Catholic Univ. of America, Washington, D.C.
20064 (F-10)
OEHSER, PAUL H., 9012 Old Dominion Dr.,
McLean, Va. 22101 (F-1, 3, 9, 30)
O’CONNOR, JAMES V., 10108 Haywood Cir.,
Silver Spring, Md. 20902 (M-6, 7)
O’HARE, JOHN, Ph.D., 301 G St. S.W., Washing-
ton, D.C. 20024 (F-40, 44)
O’HERN, ELIZABETH M., Ph.D., 633 G St., S.W.,
Washington, D.C. 20024 (M-16)
O’KEEFE, JOHN A., Code 680, Goddard Space
Flight Ctr., Greenbelt, Md. 20770 (F-1, 6)
OKABE, HIDEO, Ph.D., Rm. A-243, Bg. 222, Natl.
Bur. of Standards, Washington, D.C. 20234
(F-4)
OLIPHANT, MALCOLM W., Ph.D., 1606 Ulupii
St., Kailua, H! 96734 (F)
ORDWAY, FRED, Ph.D., 5205 Elsmere Ave.,
Bethesda, Md. 20014 (F-4, 6, 28, 39)
ORLIN, HYMAN, Ph.D., Natl. Academy of Sci-
ences, 2101 Constitution Ave N.W., Wash-
ington, D.C. 20418 (F-17)
OSER, HANS J., Ph.D., 8810 Quiet Stream Ct.,
Potomac, Md. 20854 (F-6)
OSGOOD, WILLIAM R., Ph.D., 6530 Democracy
Blvd., Bethesda, Md. 20034 (E-14, 18)
OTA, HAJIME, M.S., 5708 64th Ave., E. Riverdale,
Md. 20840 (F-12)
OWENS, JAMES P., M.A., 14528 Bauer Dr., Rock-
ville, Md. 20853 (F-7)
p
PAFFENBARGER, GEORGE C., D.D.S., ADA Res.
Unit, Natl. Bur. of Standards, Washington,
D.C. 20234 (F-21)
PAGE, BENJAMIN L., B.S., 1340 Locust Rd.,
Washington, D.C. 20012 (E-1, 6)
PARKER, KENNETH W., 6014 Kirby Rd.,
Bethesda, Md. 20034 (E-3, 10, 11)
PARKER, ROBERT L., Ph.D., Metallurgy Div.,
Natl. Bur. of Standards, Washington, D.C.
20234 (F)
PARMAN, GEORGE K., 8054 Fairfax Rd., Alex-
andria, Va. 22308 (F-4, 27)
PARRY-HILL, JEAN, Ms., 3803 Military Rd.,
N.W., Washington, D.C. 20015 (M)
PAYNE, FAITH N., 1745 Hobart St. N.W., Wash-
ington, D.C. 20009 (M-7)
PELCZAR, MICHAEL J., Jr., Vice Pres. for Grad.
Studies & Research, Univ. of Maryland, Col-
lege Park, Md. 20742 (F-16)
PEROS, THEODORE P., Ph.D., Dept of Chem-
110
istry, George Washington Univ., Washington,
D.C. 20006 (F-1, 4, 39)
PETERLIN, ANTON, Polymers Div., Inst. Ma-
terials Res., Nat. Bureau Standards, Wash-
ington, D.C. 20234 (F)
PHAIR, GEORGE, Ph.D., 14700 River Rd.,
Potomac, Md. 20854 (F-7)
PHILLIPS, Mrs. M. LINDEMAN, M.S., 2510
Virginia Ave., N.W., #507N, Washington, D.C.
20037 (F-1, 6, 13, 25)
PIKL, JOSEF, 211 Dickinson Rd., Glassboro, N.J.
08028 (E)
PITTMAN, MARGARET, Ph.D., 3133 Connecticut
Ave., N.W., Washington, D.C. 20008 (E)
PLAIT, ALAN O., M.S., 5402 Yorkshire St.,
Springfield, Va. 22151 (F-13)
POLACHEK, HARRY, 11801 Rockville Pike
Rd., Rockville, Md. 20852 (E)
POOS, F. W., Ph.D., 5100 Fillmore Ave.,
Alexandria, Va. 22311 (E-5, 6)
POLLACK, Mrs. FLORA G., Mycology Lab., Rm.
11 North Bldg., Beltsville Ars. Ctr. W. Belts-
ville, Md. 20705 (F-10)
PONNAMPERUMA, CYRIL, Ph.D., Lab. of Chemi-
cal Evolution, U. of Maryland Dept. of Chem.,
College Park, Md. 20742 (F-4, 7)
POWERS, KENDALL, Ph.D., 6311 Alcott Rd.,
Bethesda, Md. 20034 (F-6, 15)
PRESLEY, JOHN T., 3811 Courtney Circle,
Bryan, Tx. 77801 (E)
PRESTON, MALCOLM S., 10 Kilkea Ct., Balti-
more, Md. 21236 (M)
PRINZ, DIANNE K., Ph.D., Code 7121.5, Naval
Res. Lab., Washington, D.C. 20375 (M-32)
PRO, MAYNARD J., 7904 Falstaff Rd., McLean,
Va. 22101 (F-26)
PRYOR, C. NICHOLAS, Ph.D., Naval Underwater
Systems Ctr., Newport, Rl. 02840 (F-137)
PURCELL, ROBERT H., 17517 White Grounds
Rd., Boyds, Md. 20720 (F-6, 16)
PYKE, THOMAS N,., Jr., M.S., Techn. Bg. A231,
Nat. Bur. Standards, Washington, D.C. 20234
(F-6, 13)
R
RABINOW, JACOB, E. E., 6920 Selkirk Dr.,
Bethesda, Md. 20034 (F-1, 13)
RADER, CHARLES A., Gillette Res. Inst., 1413
Research Blvd., Rockville, Md. 20850 (F-4, 39)
RADO, GEORGE T., Ph.D., 818 Carrie Court,
McLean, Va. 22101 (F-1)
RAINWATER, H. IVAN, Plant Protect. & Quaran-
tine Programs, APHIS, Fed. Center Bg. #1,
Hyattsville, Md. 20782 (E-5, 6, 24)
RAMIREZ-FRANKLIN, LOUISE, 2501 N. Florida
St., Arlington, Va. 22207 (M)
RAMSAY, MAYNARD, Ph.D., Plant Prot. Quar.,
APHIS, Rm. 660, FB PPQ, USDA, Hyattsville,
Md. 20780 (F-5, 24)
RANEY, WILLIAM P., Ph.D., Office of Science
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
and Technology Policy, New Executive Office
Bldg., Washington, D.C. 20500 (M-25)
RAUSCH, ROBERT, Dept. Microbiol., Western
College of Veterinary Medicine, U. of Sas-
katchewan, Saskatoon, Sask., Canada 57N
OWO (F-3, 15, 16)
RAVITSKY, CHARLES, M.S., 1505 Drexel St.,
Takoma Park, Md. 20012 (E-32)
READING, O. S., 6 N. Howells Point Rd., Bellport
Suffolk County, New York, N.Y. 11713 (E-1)
REAM, DONALD F., Holavallagata 9, Reykjavik,
Iceland (F)
RECHCIGL, MILOSLAV, Jr., Ph.D., 1703 Mark
Lane, Rockville, Md. 20852 (F-4, 19, 27, 39)
REED, WILLIAM D., 3609 Military Rd., N.W.,
Washington, D.C. 20015 (F-5, 6)
REEVE, WILKINS, Ph.D., 4708 Harvard Rad.,
College Park, Md. 20740 (F-4)
REEVES, ROBERT G., Ph.D., U.S. Geol. Surv.,
EROS Data Ctr., Sioux Falls, So. Dak. 57198
(F-7, 36)
REGGIA, FRANK, MSEE, 6207 Kirby Rd.,
Bethesda, Md. 20034 (F-6, 12, 13)
REHDER, HARALD A., Ph.D., U.S. Natl. Museum
of Nat. Hist., Washington, D.C. 20560 (F-3, 6)
REINER, ALVIN, B.S., 11243 Bybee St., Silver
Spring, Md. 20902 (M-6, 12, 13, 22)
REINHART, FRANK W., 9918 Sutherland Rad.,
Silver Spring, Md. 20901 (F-4, 6, 39)
REINHART, FRED M., M.S., P.O. Box 591, Oak
View, Calif. 93022 (F-6, 20)
REINING, PRISCILLA, Ph.D., 3601 Rittenhouse
St., N.W., Washington, D.C. 20015 (F-2)
REMMERS, GENE M., 7322 Craftown Rd., Fairfax
Station, Va. 22039 (M)
REYNOLDS, ORR E., Ph.D., Amer. Physiol. Soc.,
9650 Rockville Pike, Bethesda, Md. 20014 (F)
RHODES, IDA, Mrs., 6676 Georgia Ave., N.W.,
Washington, D.C. 20012 (E)
RHYNE, JAMES J., Ph.D., 15012 Butterchurn La.,
Silver Spring, Md. 20904 (F)
RICE, FREDERICK A., 8005 Carita Court,
Bethesda, Md. 20034 (F-4, 6, 16, 19)
RIOCH, DAVID MckK., M.D., 2429 Linden Lane,
Silver Spring, Md. 20910 (F-3, 6)
RITT, P. E., Ph.D., GTE Labs., Inc., 40 Sylvan
Rd., Waltham, Mass. 02154 (F-6, 13, 23, 29)
RIVLIN, RONALD S., Ctr. for Application of
Math, 203 E. Packer Ave., Bethlehem, Pa.
18015 (F)
ROBBINS, MARY LOUISE, Ph.D., George Wash-
ington Univ. Med. Ctr., 2300 Eye St. N.W.,
Washington, D.C. 20037 (F-6, 16, 19)
ROBERTS, ELLIOT B., 4500 Wetherill
Washington, D.C. 20016 (E-1, 6, 18)
ROBERTS, RICHARD B., Ph.D., Dept. Terrestrial
Mag., 5241 Broad Branch Rd., N.W., Wash-
ington, D.C. 20015 (F)
ROBERTS, RICHARD C., 5170 Phantom Court,
Columbia, Md. 21044 (F-6, 38)
ROBERTSON, A. F., Ph.D., 4228 Butterworth PI.,
N.W., Washington, D.C. 20016 (F)
ROBERTSON, RANDAL M., Ph.D., 1404 Highland
Circle, S.E., Blacksburg, Va. 24060 (E-6)
Rd.,
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
ROCK, GEORGE D., Ph.D., The Kennedy Warren,
3133 Conn. Ave., N.W., Washington, D.C.
20008 (E)
RODNEY, WILLIAM S., 8112 Whites Ford Way,
Rockville, Md. 20854 (F-1, 32)
RODRIGUEZ, RAUL, 254 Torrs Sato, Baldrich,
Hato Rey, PR. 00918 (F-17)
ROLLER, PAUL S., 1440 N St., N.W., Apt. 1011,
Washington, D.C. 20005 (E)
ROSADO JOHN A., 1709 Great Falls St., McLean,
Va. 22101 (F-13)
ROSE, WILLIAM K., Ph.D., 10916 Picasso Ln.,
Potomac, Md. 20854 (F)
ROSENBLATT, DAVID, 2939 Van Ness St., N.W.,
Apt. 702, Washington, D.C. 20008 (F-1)
ROSENBLATT, JOAN R., 2939 Van Ness St.,
N.W., Apt. 702, Washington, D.C. 20008 (F-1)
ROSENTHAL, JENNY E., 7124 Strathmore St.,
Falls Church, Va. 22042 (F-13, 32)
ROSENTHAL, SANFORD M., Bidg. 4, Rm. 122,
National Insts. of Health, Bethesda, Md.
20014 (E)
ROSS, FRANKLIN, Off. of Asst. Secy. of the Air
Force, The Pentagon, Rm. 4E973, Washing-
ton, D.C. 20330 (F-22)
ROSS, SHERMAN, 24 Wessex Rd., Silver Spring,
Md. 20910 (F-40)
ROSSINI, FREDERICK D., Ph.D., Dept. Chemis-
try, Rice Univ., Houston, Tex. 77001 (F-1)
ROTH, FRANK L., M.Sc., 200 E. 22nd St., #33
Roswell, NM. 88201 (E-6)
ROTH, ROBERT S., Solid State Chem. Sect.,
National Bureau of Standards, Washington,
D.C. 20234 (F)
ROTKIN, ISRAEL, M.A., 11504 Regnid Dr.,
Wheaton, Md. 20902 (F-1, 13, 34)
ROWEN, JOHN W., Washington Towers #2407,
9701 Fields Rd., Gaithersburg, Md. 20760 (F)
RUBIN, MORTON J., M.Sc., World Meterol. Org..,
Casa Postale #5, CH-1211, Geneva 20,
Switzerland (F-23)
RUDOLPH, MICHAEL, 4521 Bennion Rd., Silver
Spring, Md. 20906 (M)
RUPP, N. W., D.D.S., American Dental Assoc.,
Research Division, Rm. A157, Bldg. 224,
National Bureau of Standards, Washington,
D.C. 20234 (F-21)
RUSSELL, LOUISE M., M.S., Bg. 004, Agr. Res.
Center (West), USDA, Beltsville, Md. 20705
(F-5, 6)
RYERSON, KNOWLES A., M.S., Dean Emeritus,
15 Arlmonte Dr., Berkeley, Calif. 94707 (E-6)
S
SAALFIELD, FRED E., Naval Res. Lab., Code
6110, Washington, D.C. 20375
SAENZ, ALBERT W., Ph.D., Radiation Techn.
Div., Naval Research Laboratory, Code
6603S, Washington, D.C. 20375 (F)
SAILER, R. I., Ph.D., 3847 S.W. 6TH PI., Gaines-
ville, Fla. 32607 (F-5, 6)
111
SALLET, DIRSE W., Ph.D., 12440 Old Fletcher-
town Rd., Bowie, Md. 20715 (M-1, 14)
SANDERSON, JOHNA., Ph.D., 303 High St., Alex-
andria, Va. 22203 (F-1, 32)
SARIMENTO, RAFAEL, Ph.D., % UNDP, Lagos
Nigeria, Box 20, Grand Central Post Office,
New York, N.Y. 10017 (F-4, 5, 24, 39)
SASMOR, ROBERT M., 4408 N. 20th. Rd. Arling-
ton, Va. 22207 (F)
SAULMON, E. E., 202 North Edgewood St.,
Arlington, Va. 22201 (M)
SAVILLE, THORNDIKE, Jr., M.S., 5601 Albia Ra.,
Washington, D.C. 20016 (F-6, 18)
SAYLOR, CHARLES P., Ph.D.,10001 Riggs Rad.,
Adelphi, Md. 20783 (F-1, 4, 32)
SCHALK, JAMES M., Ph.D., U.S. Vegetable
Lab., Highway 17 South, P.O. Box 3107,
Charleston, South CA 29407 (F)
SCHECHTER, MILTON S., 10909 Hannes Court,
Silver Spring, Md. 20901 (E-4, 6, 24)
SCHINDLER, ALBERT I., Sc.D., Code 6000, U.S.
Naval Res. Lab., Washington, D.C. 20375
(F-1)
SCHLAIN, DAVID, Ph.D., P.O. Box 348, College
Park, Md. 20740 (F-4, 20, 29, 36)
SCHMIDT, CLAUDE H., Ph.D., 1827 No. 3rd St.,
Fargo, No. Dak. 58102 (F-5)
SCHMITT, WALDO L., Ph.D., U.S. National
Museum, Washington, D.C. 20560 (E-3)
SCHNEIDER, SIDNEY, 239 N. Granada St.,
Arlington, Va. 22203 (E)
SCHNEPFE, MARIAN M., Ph.D., 2019 Eye St.,
N.W., #402, Washington, D.C. 20006 (F-4, 7)
SCHOENEMAN, ROBERT LEE, 9602 Ponca PI.,
Oxon Hill, Md. 20022 (F)
SCHOOLEY, ALLEN H., 6113 Cloud Dr., Spring-
field, Va. 22150 (F-6, 13, 23, 31)
SCHOOLEY, JAMES F., 13700 Darnestown Rad.,
Gaithersburg, Md. 20760 (F-35)
SCHUBAUER, G. B., Ph.D., 5609 Gloster Rd.,
Washington, D.C. 20016 (F-1, 22)
SCHUBERT, LEO, Ph.D., The American Univ.,
Washington, D.C. 20016 (F-1, 4, 30, 39)
SCHULMAN, FRED, Ph.D., 11115 Markwood Dr.,
Silver Spring, Md. 20902 (F-4)
SCHULMAN, JAMES H., Ph.D., U.S. Off. Naval
Res., Branch Off., 223 Old Marylebone
Rd., London, England NW1, 5TH (F-1, 32)
SCHWARTZ, ANTHONY M., Ph.D., 2260 Glen-
more Terr., Rockville, Md. 20850 (F-4, 39)
SCHWARTZ, MANUEL, 321-322 Med. Arts Bg.,
Baltimore, Md. 21201 (M)
SCOTT, DAVID B., D.D.S., 15C-1, 2 North Dr.,
Bethesda, Md. 20014 (F-21)
SCRIBNER, BOURDON F., 123 Peppercorn PI.,
Edgewater, Md. 21037 (3)
SEABORG, GLENN T., Ph.D., Lawrence Berkeley
Lab., Univ. of California, Berkeley, Calif.
94720 (F-26) ;
SEEGER, RAYMOND J., Ph.D., 4507 Wetherill
Rd., Bethesda, Md. 20016 (E-1, 6, 30, 31)
SEITZ, FREDERICK, Rockefeller University, New
York, N.Y. 10021 (F-36)
112
SERVICE, JERRY H., Ph.D., Cascade Manor, 65
W. 30th Ave., Eugene, Oreg. 97405 (E)
SHAFRIN, ELAINE G., M.S., Apt. N-702, 800 4th
St., S.W., Washington, D.C. 20024 (F-4)
SHAPIRA, NORMAN, 86 Oakwood Dr., Dunkirk,
Md. 20754 (M)
SHAPIRO, GUSTAVE, B.S., 3704 Munsey St.,
Silver Spring, Md. 20906 (F-13)
SHELTON, EMMA, National Cancer Institute,
Bldg. 37, Rm. 4C-06, Bethesda, Md. 20014 (F)
SHEPARD, HAROLD H., Ph.D., 2701 S. June St.,
Arlington, Va. 22202 (E-5, 24)
SHERESHEFSKY, J. LEON, Ph.D., 9023 Jones
Mill Rd., Chevy Chase, Md. 20015 (E-4)
SHERLIN, GROVER C., 4024 Hamilton St.,
Hyattsville, Md. 20781 (L-1, 6, 13, 31)
SHIELDS, WILLIAM ROY, A.M.S.S., 55 San
Juan, Los Alamos, NM 87544 (F)
SHMUKLER, LEON, 817 Valley Forge Towers,
1000 Valley Forge Circle, King of Prussia, Pa.
19404 (F)
SHNEIDEROV, A. J., M.M.E., 1673 Columbia Rd.,
N.W.,#309, Washington, D.C. 20009 (M-1, 22)
SHOTLAND, EDWIN, 418 E. Indian Spring Dr.,
Silver Spring, Md. 20901 (M-1)
SHROPSHIRE, W., Jr., Ph.D., Radiation Bio. Lab.,
12441 Parklawn Dr., Rockville, Md. 20852
(F-6, 10, 33)
SHUBIN, LESTER D., Proj. Mgr. for Standards,
NILECJ/LEAA, U.S. Dept. Justice, Washing-
ton, D.C. 20531 (F-4)
SIEGLER, EDOUARD HORACE, Ph.D., 201 Tulip
Ave., Takoma Park, Md. 20012 (E-5, 24)
SILVER, DAVID M., Ph.D., Applied Physics Lab.,
Johns Hopkins Univ., Laurel, Md. 20810
(M-4, 6)
SIMHA, ROBERT, Ph.D., Case Western Reserve
Univ., Cleveland, Ohio 44106 (F)
SIMMONS, LANSING G., 3800 N. Fairfax Dr.,
Villa 809, Arlington, Va. 22203 (F-18)
SIMON, BENSON J., M.B.A., 8704 Royal Ridge
Lane, Laurel, Md. 20811 (M-37)
SITTERLY, CHARLOTTE M., Ph.D., 3711 Brandy-
wine St., N.W., Washington, D.C. 20016
(E-1, 6, 32)
SLACK, LEWIS, 106 Garden Rd., Scarsdale, N.Y.
10583 (F)
SLAWSKY, MILTON M., Ph.D., 8803 Lanier Dr.,
Silver Spring, Md. 20910 (F-6, 12, 22, 31)
SLAWSKY, ZAKA I., Ph.D., 9813 Belhaven Rd.,
Bethesda, Md. 20034 (F)
SLEEMAN, H. KENNETH, Ph.D., Div. Biochem.
WRAIR, Washington, D.C. 20012 (F)
SLOCUM, GLENN G., 4204 Dresden St., Ken-
sington, Md. 20795 (E-16, 27)
SMILEY, ROBERT L., 1444 Primrose Rd., N.W.,
Washington, D.C. 20012 (M-5)
SMITH, BLANCHARD DRAKE, M.S., 5265 Port
Royal Road, Springfield, Va. 22151
SMITH, DAYNA, 1745 Pimmit Dr., Falls Church,
Va. 22043 (M)
SMITH, FLOYD F., Ph.D., 9022 Fairview Rd.,
Silver Spring, Md. 20910 (E-5, 24, 42)
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
SMITH, FRANCIS A., Ph.D., 1023 55th Ave.,
South, St. Petersburg, Fla. 33705 (E-6)
SMITH, JACK C., 3708 Manor Rd., Apt. 3, Chevy
Chase, Md. 20015 (F)
SMITH, PAUL A., 4714 26th St., N., Arlington,
Va. 22207 (F-6, 7, 18, 22)
SMITH, ROBERT C., Jr., %Versar, Inc., 6621
Electronic Dr., Springfield, Va. 22151 (F-4, 31)
SNAVELY, BENJAMIN L., Ph.D., 721 Springloch
Rd., Silver Spring, Md. 20904 (F-6, 25, 31, 32)
SNAY, HANS G., Ph.D., 17613 Treelawn Dr.,
Ashton, Md. 20702 (F-25)
SNOW, C. EDWIN, 12715 Layhill Rd., Silver
Spring, Md. 20906 (M-32)
SNYDER, HERBERT H., Ph.D., RFD. A-1, Box 7,
Cobden, IL 62920 (F)
SOKOL, PHILLIP E., Ph.D., 4704 Flower
Valley Dr., Rockville, Md. 20853 (F-4, 6, 39)
SOKOLOVE, FRANK L., 3015 Graham Rad., Falls
Church, Va. 22042 (M)
SOLOMON, EDWIN M., 5225 Pooks Hill Rd.,
Bethesda, Md. 20014 (M-4)
SOMERS, IRA I., 1511 Woodacre Dr., McLean,
Va. 22101 (M-4, 6, 27)
SOMMER, HELMUT, 9502 Hollins Ct., Bethesda,
Md. 20034 (F-1, 13)
SORROWS, H. E., Ph.D., 8820 Maxwell Dr.,
Potomac, Md. 20854 (F)
SPALDING, DONALD H., Ph.D., 17500 S.W. 89th
Ct., Miami, Fla. 33157 (F-6, 10)
SPECHT, HEINZ, Ph.D., 311 Oakridge Dr.,
Schenectady, N.Y. 12306 (E-1, 6)
SPENCER, LEWIS V., Box 206, Gaithersburg,
Md. 20760 (F)
SPERLING, FREDERICK, 1131 University Blvd.,
W., #1807, Silver Spring, Md. 20902 (F-19)
SPIES, JOSEPH R., 507 N. Monroe St., Arlington,
Va. 22201 (F-4, 19)
SPOONER, CHARLES S., Jr., M.F., 346 Spring-
vale Rd., Great Falls, Va. 22066 (F-1, 13, 25)
SPOONER, RONALD L., Ph.D., Planning Sys-
tems, Inc., 7900 Westpark Dr., McLean, Va.
22101 (M-13, 25)
SPRAGUE, G. F., Ph.D., Dept. Agronomy, Univ. of
Illinois, Urbana, III. 61801 (E-33)
ST. GEORGE, R. A., 3305 Powder Mill Rd.,
Adelphi Station, Hyattsville, Md. 20783 (F-3,
5, 11, 24)
STAIR, RALPH, 1686 Joplin St. S., Salem, Ore.
97302 (E-6)
STAKMAN, E. C., Univ. of Minnesota, Inst. of
Agric., St. Paul, Minn. 55108 (E)
STALLARD, JOHN M., Ph.D., Hdatrs., Naval
Material Command, MAT-035, Washington,
D.C. 20360 (F-6, 25)
STAUSS, HENRY E., Ph.D., 8005 Washington
Ave., Alexandria, Va. 22308 (F-20)
STEARN, JOSEPH L., 3511 Inverrary Dr., #108,
Lauderville, Fl. 33319 (E)
SmEELE; LENDELL €E.; 7624 Highland St.,
Springfield, Va. 22150 (F-20, 26)
STEERE, RUSSELL L., Ph.D., 6207 Carrollton
Ter., Hyattsville, Md. 20781 (F-6, 10, 16, 42)
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
STEGUN, IRENE A., National Bureau of Stand-
ards, Washington, D.C. 20234 (F)
STEIDLE, WALTER E., 2439 Flint Hill Rd., Vienna,
Va. 22180 (F)
STEINER, ROBERT F., Ph.D., 2609 Turf Valley
Rd., Ellicott City, Md. 21043 (F-4)
STEINHARDT, JACINTO, Ph.D., Georgetown
Univ., Washington, D.C. 20057 (F-4)
STEPHENS, ROBERT E., Ph.D., 4301 39th St.,
N.W., Washington, D.C. 20016 (E-1, 32)
STERN, KURT H., Ph.D., Naval Res. Lab., Code
6130, Washington, D.C. 20375 (F-4, 29)
STEVENS, RUSSELL B., Ph.D., Div. of Biological
Sciences, N.R.C., 2101 Constitution Ave.,
Washington, D.C. 20418 (F-10, 42)
STEVENSON, JOHN A., 3256 Brandy Ct., Falls
Church, Va. 22042 (E-6, 10)
STEWART, KENNETH R., 12907 Crookston La.,
#16, Rockville, Md. 20851 (M-25)
STEWART, T. DALE, M.D., 1191 Crest Lane,
McLean, Va. 22101 (E-2, 6)
STIEF, LOUIS J., Ph.D., Code 691, NASA God-
dard Space Flight Ctr., Greenbelt, Md. 20771
(F-4)
STIEHLER, ROBERT D., Ph.D., 3234 Quesada
St. N.W., Washington, D.C. 20015 (F-1, 4,
14, 39)
STILL, JOSEPH W., M.D., M.P.H., 1408 Edge-
cliff Lane, Pasadena, Calif. 91107 (E)
STIMSON, H. F., 2920 Brandywine St., N.W.,
Washington, D.C. 20008 (E-1, 6)
STIRLING, MATHEW W., Mrs., 3311 Rowland PI.,
N.W., Washington, D.C. 20008 (F-2)
STOETZEL, MANYAB., Ph.D., 2600 Millvale Ave.,
North Forestville, Md. 20028 (F-5)
STRAUSS, SIMON W., Ph.D., 4506 Cedell PI.,
Camp Springs, Md. 20031 (F-4)
STRIMPLE, HARRELL, L., Dept. of Geology, The
Univ. of lowa, lowa City, IA. 52242 (F)
STUART, NEIL W., Ph.D., 1341 Chilton Dr., Silver
Spring, Md. 20904 (F-10, 33)
SULZBACHER, WILLIAM L., 8527 Clarkson Dr.,
Fulton, Md. 20759 (F-16, 27)
SWICK, CLARENCE H., 5514 Brenner St., Capitol
Heights, Md. 20027 (F-1, 6, 7)
SWINGLE, CHARLES F., Ph.D., 431 Humboldt
St., Manhattan, Kans. 66502 (E-10, 11, 33)
SYKES, ALAN O., 304 Mashie Dr., S.E., Vienna,
Va. 22180 (M-25)
+
TALBERT, PRESTON T., Ph.D., Dept. of Chem.,
Howard Univ., Washington, D.C. 20059 (F-4,
39)
TALBOTT, F. LEO, R.D. #4, Bethlehem, Pa.
18015 (F-1, 6)
TASAKI, ICHIJI, M.D., Ph.D., Lab. of Neuro-
biology, Natl. Inst. of Mental Health,
Bethesda, Md. 20014 (F)
TATE, DOUGLAS R., B.A., 11415 Farmland Dr.,
Rockville, Md. 20852 (F-1)
113
TAYLOR, ALBERT L., % J. N. Sasser, Box 5397,
Raleigh, N.C. 27607 (E-15)
TAYLOR, B. N., Ph.D., Bg. 220, Rm. B258, Nat.
Bureau Standards, Washington, D.C. 20234
(F-6, 13)
TAYLOR, JOHN K., Ph.D., Chemistry Bldg., Rm.
B-326, Natl. Bur. of Standards, Washington,
D.C. 20234 (F-4, 29)
TAYLOR, LAURISTON S., 7407 Denton Rad.,
Bethesda, Md. 20014 (E)
TCHEN, CHAN-MOU, City College of New York,
Mechanical Engr. Dept., New York, N.Y.
10031 (F)
TEAL, GORDON K., Ph.D., 5222 Park Lane,
Dallas, Tex. 75220 (F-13, 29)
TEITLER, S., Code 4105, Naval
Washington, D.C. 20375 (F)
THAYER, T. P., Ph.D., U.S. Geological Surv.,
Mail Stop 954, Reston, Va. 22092 (F-7)
THEUS, RICHARD B., 8612 Van Buren Dr., Oxon
Hill, Md. 20022 (F)
THOMPSON, F. CHRISTIAN, Ph.D., 4255 S. 35th
St., Arlington, Va. 22206 (F-3, 5)
THURMAN-SCHWARTZWELDER, E. B., 30 Ver-
sailles Blvd., New Orleans, La. 70125 (E-5, 6)
TILDEN, EVELYN B., Ph.D., 1100 Alvarado S.E.
#304, Albuquerque, NM 87108 (E)
TITUS, HARRY W., 7 Lakeview Ave., Andover,
N.J. 07821 (E-6)
TODD, MARGARET RUTH, Miss, P.O. Box 687,
Vineyard Haven, Mass. 02568 (F-7)
TOLHURST, GILBERT, Ph.D., 7 Red Fox Lane,
Amherst, Mass. 01002 (F-25, 40)
TOLL, JOHN S., Ph.D., Pres., State Univ. of New
York, Stony Brook, L.I., N.Y. 11794 (F-31)
TORRESON, OSCAR W., 4317 Maple Ave.,
Bethesda, Md. 20014 (E-6)
TOUSEY, RICHARD, Ph.D., Code 7140, Naval
Res. Lab., Washington, D.C. 20375 (F-1, 32)
TOWNSEND, MARJORIE R., B.E.E., 3529 Tilden
St., N.W., Washington, D.C. 20008 (F-13, 22)
TRAUB, ROBERT, Ph.D., 5702 Bradley Blvd.,
Bethesda, Md. 20014 (F-5)
TREADWELL, CARLETON R., Ph.D., Dept. of
Biochemistry, George Washington Univ.,
2300 Eye St., N.W., Washington, D.C. 20037
(F-4, 19)
TRENT, EVAN M., Mrs., P.O. Box 1425, Front
Royal, Va. 22630 (M)
TRUEBLOOD, EMILY E., Ph.D., 7100 Armat
Dr., Bethesda, Md. 20034 (E-6, 19)
TRUNK, GERALD, Ph.D., 503 Tolna St., Balti-
more, Md. 21224 (F)
TUNELL, GEORGE, Ph.D., Dept. of Geol. Sci.,
Univ. of California, Santa Barbara, Calif.
93106 (E-7)
TURNER, JAMES H., Ph.D., 11902 Falkirk Dr.,
Potomac, Md. 20854 (F)
UHLANER, J. E., Ph.D., U.S. Army Res. Inst. for
' Behavioral and Soc. Sci., 5001 Eisenhower
Ave., Alexandria, Va. 22333 (F-40, 44)
Res. Lab.,
114
V
VACHER, HERBERT C., 19225 N. Cave Creek
Rd., No. 89, Phoenix, Arizona, 85024 (E)
VAN DERSAL, WILLIAM R., Ph.D., 6 S. Kensing-
ton St., Arlington, Va. 22204 (F-6)
VAN TUYL, ANDREW H., Ph.D., 1000 W. Nolcrest
Dr., Silver Spring, Md. 20903 (F-1, 6, 22)
VEITCH, FLETCHER P., Jr., Ph.D., Dept. of
Chemistry, Univ. of Maryland, College Park,
Md. 20742 (F-4)
VIGUE, KENNETH J., Dir., Internatl. Projects, ITT
Corp., ITT Bldg., 1707 L St., N.W., Washing-
ton, D.C. 20036 (M-13, 31)
VINCENT, ROBERT C., Dept. Chem., George
Washington Univ., Washington, D.C. 20006
(F)
VINTI, JOHN P., Sc.D., M.I.T. Bldg., W91-202,
Cambridge, MA 02139 (F-1, 6)
VISCO, EUGENE P., B.S., 2100 Washington
Ave., Silver Spring, Md. 20910 (M-1, 34)
VON BRAND, THEODOR C., M.D., Ph.D., 8606
Hempstead Ave., Bethesda, Md. 20034 (E-15)
VON HIPPEL, ARTHUR, Ph.D., 265 Glen Rad.,
Weston, Mass. 02193 (E-6)
W
WACHTMAN, J. B., Jr., B. 306, Matls. Blidg.,
National Bureau of Standards, Washington,
D.C. 20234 (F)
WAGMAN, DONALD D., 7104 Wilson Lane,
Bethesda, Md. 20034 (F-4)
WAGNER, A. JAMES, NOAA Nat. Weather Serv.,
Nat. Meteorol. Ctr., W31, World Weather Bg.,
Washington, D.C. 20233 (F-6, 23)
WALKER, E. H., Ph.D., Friends House, 17330
Quaker Lane, Sandy Spring, Md. 20860 (E-10)
WALKER, JOHN D., Martin Marietta Corp., 1450
S. Rolling Rd., Baltimore, Md. 21227 (F)
WALTHER, CARL H., Ph.D., 1337 27th St., N.W.,
Washington, D.C. 20007 (F-6, 18)
WALTON, W. W., Sr., 1705 Edgewater Pkwy.,
Silver Spring, Md. 20903 (F-4, 6, 41)
WARGA, MARY E., 2475 Virginia Ave., N.W.,
Washington, D.C. 20037 (F-32)
WARING, JOHN A., 8502 Flower Ave., Takoma
Park, Md. 20012 (M-12, 30)
WARSHAW, STANLEY I., 1519 West Kersey Lane,
Potomac, Md. 20854 (F-6, 28, 36)
WATERWORTH, HOWARD E., Ph.D., 10001
Franklin Ave., Seabrook, Md. 20801 (F-6, 42)
WATSON, ROBERT B., 1167 Wimbledon Dr.,
McLean, Va. 22101 (E-6, 13, 25, 31)
WAYNANT, RONALD W., Ph.D., 13101 Claxton
Dr., Laurel, Md. 20811 (F13, 32)
WEAVER, E. R., 6815 Connecticut Ave., Chevy
Chase, Md. 20015 (E-4, 6)
WEBB, HAMILTON B., 4701 Willard Ave., Apt.
1406, Chevy Chase, Md. 20015 (M-6)
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
WEBB, RALPH E., Ph.D., 21P Ridge Rad.,
Greenbelt, Md. 20770 (F-5, 24)
WEBB, RAYMON E., Ph.D., Agr. Res. Center,
Vegetable Lab., Bldg. 004, Rm. 220, Belts-
ville, Md. 20705 (M-6, 10, 42)
WEBER, EUGENE W., B.C.E., 2700 Virginia Ave.,
N.W., Washington, D.C. 20037 (F-6, 12, 17, 18)
WEBER, ROBERT S., Box 142, Harlingen, TX.
78550 (M-6, 13, 17)
WEIDA, FRANK, 19 Scientists Cliff, Port Repub-
lic, Calvert County, Md. 20676 (E-1)
WEIDLEIN, E. R., Weidacres, P.O. Box 445,
Rector, Pa. 15677 (E)
WEIHE, WERNER K., 2103 Basset St., Alexandria,
Va. 22308 (E-32)
WEINBERG, HAROLD P., B.S., 1507 Sanford Rd.,
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WEINTRAUB, ROBERT L., 305 Fleming Ave.,
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WEIR, CHARLES E., Rt. 3, Box 260B, San Louis
Obispo, Calif. 93401 (F)
WEISS, ARMAND B., D.B.A., 6516 Truman Lane,
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WEISSLER, ALFRED, Ph.D., 5510 Uppingham
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WELLMAN, FREDERICK L., Dept. of Plant
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mantown, Md. 20767 (F-6, 20, 26)
WEST, WILLIAM L., Dept. of Pharmacology,
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ton, D.C. 20059 (M-19, 26, 39)
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J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
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115
INFORMATION ON THE NEWLY AFFILIATED SOCIETIES
Potomac Division, American
Phytopathological Society
Objectives: To bring together plant
pathologists to discuss research in plant
pathology and other problems of general
interest and to stimulate understanding
with other sciences concerned with the
general problem of crop improvement.
Members: Active members must be
members of the American Phytopatho-
logical Society. Persons who are not
members of the APS but are interested in
plant pathology are eligible for Associate
Membership. Retired plant pathologists
are considered honorary members.
There are 238 members (from D.C.,
Md. -Va., Del, NeJ.; N-G., & Yonkers,
N.Y.) in the Division.
Meetings: One principal meeting is held
each year with formal programs of
scientific interest. At the 1976 meeting
held at the Univ. of Delaware on March
17-19, a total of 50 papers were pre-
sented before various groups.
Metropolitan Washington Chapter of the
Society for General Systems Research
Objectives: (1) To investigate the
isomorphy of concepts, laws and models
from various fields, and to help in useful
transfers from one field to another: (2)
to encourage development of adequate
theoretical models in fields which lack
them: (3) to minimize the duplication of
theoretical effort in different fields: and
(4) to promote the unity of sciences
through improving communication among
specialists.
Members: The membership is composed
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people whose interests are broader than a
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suing the systems point of view for
116
dealing with complex problems. There
are now 100 members in the Washington
Chapter.
Meetings: The chapter sponsors an
annual meeting at which papers are pre-
sented and research areas discussed. The
1975 meeting held Sept. 19-20 was con-
cerned with ‘‘Systems Science and the
Future of Health.’’ The topic of the 1976
meeting is to be ‘‘Complexity: A
Challenge to the Adaptive Capacity of
American Society.”’
Potomac Chapter, Human
Factors Society
Objectives: To (1) provide a professional
forum for the exchange of multidis-
ciplinary ideas and information about
man and his environment: (2) encourage
a social relationship where members can
meet and communicate freely with others
who have a wide variety of viewpoints
and backgrounds: (3) establish a point of
contact for persons and organizations in
the Potomac Chapter area who are
interested in or have a need for human
factors research and technology.
Members: Must be members of the
National Society. Individuals not qualify-
ing for the election to the grade of mem-
ber who are interested or active in the
field may become associate members.
Such members may not vote or become
officers. The chapter consists of 181
members.
Meetings: Not less than one regular
meeting is held each year. Special meet-
ings may be called on request of 15
members. The principal 1975 meeting
was a one day symposium on ‘‘Advance
Technologies in Systems Operation and
Control.’’ In 1976 there was a one-day
symposium on ‘“‘Training: Technology to
Policy.”
J. WASH. ACAD. SCI., VOL. 67, NO. 3, 1977
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VOLUME 67
Number 4
Jour nal of the DECEMBER, 1977
WASHINGTON
ACADEMY... SCIENCES
Issued Quarterly
at Washington, D.C.
CONTENTS
Features:
Rae EODSON: A Century of Cryogenics 2... 22 fee hh i es
RICHARD H. McCUEN: Polynomial Regression Analysis Using a Principal
GomponentsyRotation’: 2 uh sac os shaw.e fee ins weigh sie ew Oe aide rate aoe
Research Reports:
K. N. DERUCHER: Microcracking of Concrete .................00. eee eee 135
T. J. FREST and H. L. STRIMPLE: Prokopicrinidae, New Family of
?Camerate Crinoids, Silurian (Wenlockian-Ludlovian), Tennessee and
OKANO are oy ent een neat rele eye niecasene Senne eh ceotici tenn chads Ua
JAY ABERCROMBIE: Mryiasis in the Eastern Box Turtle Caused by
Phaenicia coeruleiviridis (Diptera: Calliphoridae)......................
OWEN DEVER SHOLES: Parasitism of Trirhabda_ virgata WLeConte
-(Coleoptera: Chrysomelidae) by a Species of Aplomyiopsis Villeneuve
(Dipterasmachimidae) tec netomat cts cc ous Gatto eh et tite: She cea ac atye 2
Academy Affairs:
INRA BELONG ER SIS ls ete RT Oe Ce an aR MCR SOU! A
Information on Societies Recently Affiliated .....................0 000 eee ise)
SCIENUISESEITIELNE ENEWS) oc seus ee We Sins. Se natn See ad orale s bene nne: thetene Bp 160
Obituary:
WAAR OS ROOGE 1. eh aidinc ues sexe aacee ucore Wises giuliani atta an adage culeoer wcste
Washington Academy of Sciences
EXECUTIVE COMMITTEE
President
Richard H. Foote
President-Elect
Mary H. Aldridge
Secretary
Kelso B. Morris
Treasurer
Alfred Weissler
Members at Large
George Abraham
Grover C. Sherlin
BOARD OF MANAGERS
All delegates of affiliated
Societies (see facing page)
EDITOR
Richard H. Foote
EDITORIAL ASSISTANT
Elizabeth Ostaggi
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Founded in 1898
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This journal, the official organ of the Washington Aca- i
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is $15.00.
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_ Washington Academy of Sciences, 9650 Rockville Pike, Washington, D.C. Second class
postage paid at Washington, D.C. and additional mailing offices.
DELEGATES TO THE WASHINGTON ACADEMY OF SCIENCES,
REPRESENTING THE LOCAL AFFILIATED SOCIETIES
BuEMNBpiical Society Of WashingtOM (2)... 2626s 2 ee wee gia ce a lee oe Wyape a Gee HE Ed lee we James F. Goff
Peininemolarical Society ‘of Washington: oo: 2.0205. 0.4 cb ed ee cee t eee eee tewnes Jean K. Boek
Peimricatayaciety Of WaShINB(ON |... o5..5.552 steko tk eee eee eh eae cae sn odes William R. Heyer
PEUEMMMTIENGCICLY OF VWASMINGCON, 2: < 5462.6 ols foc one wice Ub dic oe be bnew eu wnpewmeecann David H. Freeman
Panmaiaimetcal Society Of Washington .. 22... 2.26 ee Se ce cede ween ewes Maynard Ramsay
Me ES COCEADING SOCICLY ia. cic Nie nial hors sield ote mine bie wee eid aie Sis bee Hb aledde Food wielhbe T. Dale Stewart
Pmmriemesgcicty, Of Washington: . 2... 2.62265. cc ee cee ce Sete cess beaeenes Marian M. Schnepfe
memedmancicty of the District of Columbia~ ...... 2... 62 Succ wc ce meee eee eeececenend Inactive
DE MBIBIAISIOLICAl SOGICLY 222.2 <5 21s ool. vine ke obs a vhelee we ce ees eae caus Senuweuen ded Paul H. Oehser
PEG AIESOCIety. Of WASMIMGLONM. .. 5.6.2 cca ete cee ec ce eee ceed eee uneivesenens Conrad B. Link
EMMI AIMCHICAN POFESICTS. 5.622665 she eccw cee s sa eke teed ene Ac ew auc e swe es Thomas B. Glazebrook
eM MES OCICLY OMMENOINCEES) 20 oe on se ee Mie ein inls eda ae ee wee ke ee hws George Abraham
insumnerorbiectrical and Electronics Engineers ........ 4.0006 0/2226 cect ee eee George Abraham
Pomtemeanasociety of Mechanical Engineers ......-.. 2.20500. cc ccc cece cece we eceueesces Michael Chi
emninoopical Society of Washington. ..........0.0.. 0.5 cece ceca ccc eee eeeee Robert S. Isenstein
ReICMeAIESOCICLY TON MICFODIOIOPY =... 28 es. fine ce eee eke ee elects Michael Pelzcar
Society of American Military Engineers ..................002ceceees ee te eee H. P. Demuth
PeuChie ME SOCIOL Ol Civil ENEMEETS 6). 6 ses ee ew ee eee eevee Robert Sorenson
Bociernyior experimental Biology and Medicine ....2...........56.0050 0005 ccc eeeeees Donald Flick
PERG SOLET STAVE Oy 14 (11 TNS ee Glen W. Wensch
intermmational Association of Dental Research ...........0..2..0000 cee e ee enaes William V. Loebenstein
American Institute of Aeronautics and Astronautics ... 2.2... 6.066. c eee ees George J. Vila
Panencan Meteorological SOCIeLy 2... 6c. hs. hes cc ee ee ees cn ete ee hea eeuevbes A. James Wagner
MSCeHcIgeMOClety OF WaShINGtON ©. i... 625. c eee ne ede ees ose deve w ee saeeues Robert J. Argauer
PeaustcealeSociety Of America... 2.5.25... leleec cc bese ccc cess uasaceredeevas Delegate not appointed
Pathe INC LE ATO OGICUY, [ere ose ts ion ate oats fe wide eo telgpd aie eee a Stews wis eels ae ba boewlas Dick Duffey
Eastiiieron Food LechnolopistS .. 0... 5.0.6. wb we ces chon c sees cule beuwsreen William Sulzbacher
2 ATUS TILES, (CGIPLTENIS. SOITTS NF REE oe ol ee Per aA oe er dose Cg ee Pee ra Inactive
LE CBEUPTIS WERE SL SSOLCU ELI aioe OPE DE ee cee cc a Delegate not appointed
Se SMBCIOnpLIStOny Ot SCIeENnce CIUD <6... 623 ccc sesh ence oes nde usin s ofits cece ceviewmee Inactive
paneteanvassociation Of Physics Teachers. 12... 24. .ecs esis cee tates ec eee ce ee beac To be appointed
lie OCIC VE OlVATME TIC A har ea iin sc oes eae ected wo Sideacln cy sic it dock dhal pally 4. 0! serie! wis Lucy B. Hagan
Puneticanesociery Of Plant Physiologists = 2.22052. 5 sees elec eee de see ka ws esas Walter Shropshire
Pvashimeton Operations Research Council ...:). 250.62 622d see eee eee ee eee ees John G. Honig
ISR ETHASOCICU Ol AMCEIGAs a hs ihie ic tn ew hive sO lee cee ss Ses « Sled ve PRM wa a Sb a ew ae Inactive
American Institute of Mining, Metallurgical
AMEECHO UME MPINCENSE Maer a aes shia, fen. ck wale Cae oe chad e Mekmel ge Gk ee Ss Philip W. Guild
Ravicnal meapiOlAStTONOMENS: 45 v4. oslo = cess serene s SS ee se a oa ace ane vee s Benson J. Simon
Riathiematical ASSOCiation Of AMERICA) 2.06.6 os oe eee Wee ca ce eyo ce anes d eae Patrick Hayes
ie Orman Stititie "Or CMEMMISUS. 92) capes aye oily eke, cies le saath oR os este ls teen lin pee oo 8 Miloslav Recheigl, Jr.
MMO ESVCHOIOLICAlPASSOCIALI OM co5 55 ofvse cc o0% wheels, ete npege tim dass e aya ecPaave Wee yreleis » wLele ae Gon «peal eee John O’ Hare
ihe Washington Paint Technical Group ...2......6 2. cmc. de cows bee dete neerewuees Paul G. Campbell
Amencan ehytopathological Society: =... 4 s52 es onl oe cee dee eee wee eee Tom van der Zwet
Society for General Systems Research ... 2... ... 0.002020 cece bee wee cw cwews Ronald W. Manderscheid
PARTUM CLOSES OCICUN al tie souk Br cir Geo acs afrapel zie, sid N ee ate Slama sw Sieh a Cran RE ante o H. Mcllvaine Parsons
Delegates continue in office until new selections are made by the representative societies.
f. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977 117
A Century of Cryogenics’
R. P. Hudson
FEATURE
Chief, Heat Division, National Bureau of Standards, Washington, D. C. 20234
Bicentennial themes being in vogue
these days, something of that nature
might be expected of me on this occasion.
In the case of cryogenics, the topic
of my choice, there is an obvious and
insuperable problem, however. Facing
facts, therefore, and with the thought
that ‘‘half a loaf is better than none,”’
we must settle for a single century!
I propose to give you a rapid, not
heavily technical survey of the major
developments in the history of low
temperature physics. Given the com-
plexity of the subject and the short time
available, the treatment must be ex-
tremely superficial but perhaps, in its
variety, you will find it interesting.
The phrase low temperature means
quite different things to the layman and
the physicist. The latter is talking about
the region near absolute zero—perhaps
a few words here about temperature itself
will be helpful. Scientists measure tem-
perature upward from absolute zero,
avoiding negative numbers, thus the term
absolute temperature. Apart from this,
the scientific (or thermodynamic, or
Kelvin) scale is the same as the Celsius
scale. In Table 1 is a chart of equivalent
temperatures on the most familiar and
widely used scales.
' Address of the retiring president, Philosophical
Society of Washington, January 16, 1976. Many
illustrations used in the course of the oral pre-
sentation have been omitted from this printed
version.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
A very great part of low temperature
research is carried out between 0 and 1K.
The question naturally arises, ‘‘What is
So interesting about that last one degree?’’
Here, it helps to think in terms of energy
—the quantity kT (where k is the Boltz-
mann constant, equal to 1.38 x 107%
erg K~!), which can be considered as the
quantum of thermal energy, expresses
the “‘shaking up effect’’ of the tempera-
ture, T. Whether a particular temperature,
T, can cause any significant excitation
within a system will depend upon what
system we are talking about—i.e., upon
the relative size of the thermal energy,
kT, and that of the dominant energy
States of the system.
Different physical phenomena occur in
different regions of the temperature
scale because the pertinent, allowed
energy states are of tremendously vary-
ing energy magnitude. So we must purge
our thoughts of this everyday, humanistic
concept that one degree is always ‘‘small
beans,’ although it certainly is in a 300°
world. Let us look at the diagram of
Fig. 1. Here the temperature scale is
depicted logarithmically. Life on earth
dwells within a small part of a single
decade and all major industrial activities
span less than two decades. ‘‘Cryo-
genics’’ is 100K on down, and “‘‘cryo-
physics’’ 4K on down, in usual parlance.
As a final introductory remark, I shall
now and again use the term entropy,
which is one of the thermal state de-
119
Table 1.—Temperature equivalents.
ae ; 5/9 of #
Spt Eh ‘Fahrenheit # of °F in preced- Celsius Kelvin
. Descriptor - temperature above 32°F ing column temperature temperature
Melting point of gold 1947.97°F TOS 97 1064.43 1064.43°C 1337.58K
Melting point of lead 621.504°F 589.504 327.502 327.502°C 600.652K
Boiling point of water 212° 180 100 100°C 373219 K
Typical summer day
temperature 86°F 54 30 30°C 303.15K
Typical winter day i
temperature 41°F 9 5) ae 278.15K
Freezing point of water 32°F 0 0 WE 273.15K
‘‘Forty below” —40°F = 1/2 —40 —40°C 233.15K
Boiling point of oxygen —297).532) = SS — 182.962 —182.962°C 90.188K
— 452.067 — 484.067 —268.926°C
Boiling point of helium
scriptors of a system and which is fre-
quently much more revealing than T. In
Fig. 2 I present some definitions, within
the language of thermodynamics. [From
a Statistical mechanics point of view
we know that S is a measure of disorder.]|
Certain commonly encountered experi-
mental manipulations at low temperatures
are most perspicuously diagrammed on
an entropy plot.
Early Developments
The history of the development of
low-temperature physics is intimately
bound with the liquefaction of gases,
especially the so-called ‘‘permanent
gases.”
At the end of 1877 (note the desirable
century span!) a permanent gas was first
liquefied, by expansion from high pres-
sure. This was achieved almost simul-
taneously, for air (as a fog) by Cailletet
in France and for oxygen (as a liquid jet)
by Pictet in Switzerland. In April
1883, in Cracow, the Polish scientists
Wroblewski and Olzewski convincingly
liquefied (i.e., collected) oxygen, and
then nitrogen.
Hydrogen remained obdurate until
1898 when Dewar succeeded, using the
expansion-plus-regenerative-cooling tech-
nique (below). In the meantime, Ramsey
had, in 1895, isolated the elemental
substance helium, but this was to remain
unliquefiable for another decade.
120
— 268.926 4.224K
The Liquefaction Process
The diagram in Fig. 3 represents a
hypothetical fluid on an S-T chart. The
curve is a line of fixed pressure, say, 1
atmosphere. Consider a simple expan-
sion of a compressed, thermally-isolated
gas at some starting temperature, T):
reduction of the pressure, P, causes an
excursion from right to left on a horizontal
(constant entropy) path and expansion to
1 atmosphere brings the system to the
1 atmosphere line CDA. If the section
CD is encountered, we shall have reached
the normal boiling point, T,, and have
produced liquid. However, if this graph
represents nitrogen, for instance, and T)
represents room temperature, one would
require a pressure of 10° atmospheres
to reach point B!
The heat exchanger, or heat regenera-
tor, principle enables one to use much
smaller pressure ratios:- the expanded
gas is used to precool incoming gas,
which starts its expansion at a lower
temperature and hence cooling is pro-
gressive.
The lower the boiling point, the harder
it is to make the liquefaction process
work without excellent thermal insula-
tion. The necessary insulation is fur-
nished by a container which is common to
the domestic scene and familiar to us all
as the thermos or vacuum flask. It was
first used in this connection by Dewar in
1892; scientists today call them dewar
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
TEMPERATURE PHENOMENON
Tungsten boils (6200 K)
Tungsten melts (3650 K)
Gold melts (1337 K)
10° a irom Curie point (1043 K)
Mu metal Curie point (673 K)
Water boils (1 atm.)
eee Ce Me Tes
Baie it M40 ‘bedow’
as ~DyCo> Curie point (154 K)
10”
Oxygen normal boiling
point (90.2 K)
as Oxygen solidifies (54.4 K)
NdN Curie point (35 K)
ee Hydrogen normal boiling point
ee ~Hydrogen solidifies (14 K)
10
4He normal boiling point (4.2 K)
——————————! ‘He superfluid transition
ees Cadmium superconducting transition (0.515 K)
|
0.1
ae Beryllium superconducting transition
0.024 K
0,01 Sem TAL Curie point
CMN Curie point
0.001
Fig. 1. Temperatures of occurrence of representative physical phenomena.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977 121
ENTROPY
IRREVERSIBLE AQ
AS 2 T
REVERSIBLE
ANS = AQ
Q
i : pu aa oa
AT AT
HEAT
CAPACITY
Fig. 2. Definition of entropy, S, and its rela-
tionships with heat energy, Q, heat capacity,
C, and temperature, T.
vessels, or dewars. It may not be an
exaggeration to assert that this device is
the single most important technological
advance for the field of low temperature
physics. The lowest boiling point fluids
require double (i.e., nested) dewars for
efficient liquefaction and for economical
storage. In 1908, helium was first lique-
fied, at Leiden where Kamerlingh Onnes
had for 20 years been building up the
world’s leading low-temperature labora-
tory. The boiling point was measured
to be 4.2K. At that time only 12 cubic
feet of gas were available, painstakingly
extracted from monazite sand, and the
yield was about one pint of liquid.
Why, one might ask, are low tempera-
ture liquids in general important for
cryogenic research? The main reasons
are 4-fold: by reason of their latent heat
of evaporation, they absorb heat from
the surroundings at constant temperature
and permit one to maintain a low
temperature; the temperature is readily
controllable by controlled pumping; the
temperature can be further reduced by
pumping; and, finally, the temperature
can be measured in terms of the vapor
pressure. Subjected to vigorous pumping
(forced evaporation), most liquids even-
tually cool to a point where they become
solid, i.e., freeze. But not helium!
122
Kamerlingh Onnes discovered early on
that it was still liquid when cooled to
0.7K. Today we know that, unless it is
subjected to pressures in excess of 25
atmospheres, helium will remain liquid all
the way down to absolute zero.
Metals and Superconductors
Around the turn of this century, it
was known that the electrical resistivity
of metals decreased with falling tempera-
ture. The question remained: What
happened at very low temperatures?
There were various theories: a) the re-
sistivity would fall continuously, b) the
resistivity would pass through a minimum
and then rise again, c) the resistivity
would ‘‘flatten out’’ to a steady value! In
1911 Kamerlingh Onnes undertook to find
out. He discovered that the resistance
of platinum became constant but, also,
that constant value was dependent upon
the purity of the specimen. Next, for a
metal of the highest then-achievable
purity Kamerlingh Onnes selected mer-
Fig. 3. Entropy vs. temperature curve (schematic)
of a hypothetical fluid under constant pressure,
say, 1 atmosphere; then Ty, is the normal boiling
point.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
cury. The results were as shown in
Fig. 4—at a temperature close to the
normal boiling point of helium, the re-
sistance dropped to an immeasurably
small value. The phenomenon was at
first attributed to a short-circuit de-
veloping somewhere in the cumbersome
measurement system and much fruitless
effort was expended to locate and cure
‘“‘the fault.”” Kamerlingh Onnes found
this breakdown very disagreeable and, in
the Dutch phrase of a Leiden worker’
in the early years, zat en zak en as! With
such disbelief was made one of the
greatest scientific discoveries of the ages!
Many years later it became possible
to demonstrate that this extremely small
resistivity was, in fact, zero to a very high
order of accuracy. Obviously, metals
with zero resistance offer great electrical
engineering advantage, but such a prop-
erty was of great interest to physicists
as their thoughts ran on, first to enormous
electric currents and then to very intense
magnetic fields —all for free, so to speak.
This naive hope was soon dashed by the
further researches of Kamerlingh Onnes
and his associates in the period 1913-
1914, into the effect on this super-
conductivity of the size of the current
being carried and also of an external
magnetic field. In brief, they found that
superconductivity was readily suppressed;
Silsbee of NBS showed in 1916 that it
was the magnetic field at the surface of
the conductor (whether generated ex-
ternally or produced by a current within
the conductor) that was the behavior-
determining factor.
The lowest value of H which could
suppress superconductivity was termed
the critical field, H,. This was found to
vary from zero at a certain temperature
termed the transition temperature, T.,
in parabolic fashion to a value Hp at
the absolute zero (by extrapolation, of
course). Some representative curves are
shown in Fig. 5. In general, a substance
exhibiting a high value for T, has a high
H,, and vice versa. Thus, the values of
2 J. A. Kok: Literal translation: . . . sat in sack-
cloth and ashes. .. .
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
R/Roeo
0-02
Pt
0-01
Hg
ee ee) Sra EES 2 ee ee beer td
10 20° KR:
Fig. 4. Resistivity ratio (for a normalization
temperature of 0°C) for platinum and for mercury
(by Kamerlingh Onnes; after D. Shoenberg, Super-
conductivity [Cambridge University Press, 1952],
pe 2).
these quantities are: for lead, 7K and 800
gauss; and for tungsten, 15 mK and 1.2
gauss.
Meissner and Ochsenfeld discovered in
1933 that a metal, upon being cooled to
the superconducting state, expels all
magnetic flux from itself. This is actually
a much more ‘“‘restrictive’’ property than
would be required simply as a conse-
quence of electrical resistance (or electric
field within) being equal to zero. In the
terminology of electromagnetic theory,
B = O rather than merely dB/dt = 0.
As, up to a limit, a magnetic field
cannot penetrate a superconductor, the
latter may be used to repel a solid
magnet (or a coil which is generating a
magnetic field). For years, the only con-
sequence of this was the fascinating
laboratory demonstration of the ‘‘floating
magnet’’ but, as we shall see later, even
more striking applications of this prop-
erty, and of possibly great practical
value, are at hand.
With the passage of time, more and
more elements were discovered to be-
come superconductors if they were
cooled to sufficiently low temperatures.
Compounds and alloys are continually
being added to the list. Approximately
123
oersted
., 500
H
4..§ .- 6 «
Fig. 5. Temperature dependence of the critical magnetic field; H,, for selected
superconductors (after H. M. Rosenberg, Low Temperature Solid State Physics
[Clarendon Press, Oxford, 1965], p. 150).
One quarter of the known chemical ele-
ments are superconductors at low tem-
perature, although a few of these, it is
true, are only so when subjected to very
high pressure.
Magnetism
This subject also fascinated the Leiden
physicists. Very many substances are
paramagnetic (i.e. demonstrating mag-
netic properties when ‘‘encouraged’’ by
an applied magnetic field. The latter is
124
unnecessary in the case of the magnetic
substances most familiar to the layman,
which are termed ferromagnets.). The
paramagnetism arises because the constit-
uent atoms are little permanent magnets
(magnetic ‘‘moments’’ in the technical
jargon, symbol 2). An external magnetic
field lines up the atomic magnets and the
thermal energy opposes this. There en-
sues a struggle for supremacy between
the energies wH and kT. Their ratio,
wH/kKT, inserted into a simple theory,
with mathematics the same as for the
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
molecular gas, went a long way to
explaining the early observations, made
upon numerous substances. In particular,
this theory yielded the Curie Law
(magnetic susceptibility inversely pro-
portional to temperature) and did rea-
sonably well in describing the departures
therefrom (saturation effects) in high
magnetic fields.
Kamerlingh Onnes wanted to probe
more deeply, to look for surprises (like
superconductivity), and to see how and
where the new-fangled quantum theory
entered the picture. He also felt that
magnetic saturation and superconduc-
tivity must have acommon basis. A great
deal of research on magnetism was
carried out in Leiden just before and after
World War I. The laboratory fell behind
in this particular field for a time in the
mid-1920’s but had come back to the
forefront by 1933, just in time to miss the
Nobel Prize! This reference is to the
magnetic method of producing tempera-
tures far below those achievable with
liquid helium alone, about which we shall
now say a few words.
Magnetic Cooling
A cursory thermodynamic treatment of
this topic had long been available and
Kuenen laid it out in detail in 1922.
The essence is as follows:
Starting from the ‘‘Maxwell relation’’
OT OM
(oa), ~~ Gas)
one derives
OT T (OM
laa), ~ lar),
cH
Bcur
if M = cH/T, the Curie Law. Here c is
the ‘“‘Curie constant,’ C, is the heat
capacity at constant magnetic field and
M is the magnetic moment.
The equation enables us to calculate
the rise in temperature occasioned by
application of a magnetic field under
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
conditions of isolation from the surround-
ings (constant entropy, S). The reverse
‘of this procedure is the process of
magnetic cooling. The effect is small
except at low temperatures where, as
scientists Debye and Giauque independ-
ently concluded in 1926, it would con-
stitute a useful process for further re-
frigeration. Seven years later, the first
experimental demonstration was achieved
by Giauque himself, pipping Leiden by
2% weeks!
In the early 1930’s, Hitlerism was the
direct cause of the establishment of a
very productive low temperature labora-
tory in Oxford—the Clarendon—with
the influx of physicists to England from
Germany and elsewhere. Much of the
work in Oxford, over a long period, was
aimed at the refinement and utilization
of magnetic cooling. Again, we may
advantageously refer to an entropy
diagram, Fig. 6. This is similar to the
one employed earlier for fluids but now,
instead of liquefaction, the ‘‘condensa-
tion’? phenomenon is one of magnetic
ordering. At a low starting temperature
(say, IK or 2K), Tj, the entropy of a
paramagnet, is essentially just that arising
from the atomic magnets, the lattice
entropy having all but vanished. A mag-
netic field is applied isothermally, lower-
ing the entropy and bringing the system
from point A to point B. The para-
magnetic ‘“‘working substance’ is now
isolated from the surroundings (which
remain at temperature T,) and the
magnetic field is reduced to zero. The
system thereupon moves along a line of
constant entropy to reach the zero-field
curve at point C. The temperature has
thus fallen dramatically, to T;.
The weaker the paramagnetism (smaller
ju, few magnetic atoms per unit volume
of substance) the lower will be the
temperature region in which the S curve
falls off, i.e., the lower T;. There are,
however, compensating disadvantages
such as reduced heat content (enthalpy),
or ability to absorb heat leakage from
the surroundings. What magnitude of
heat leak can be tolerated? In a typical
experimental arrangement, a convenient
125
Rin(2J+1)
ENTROPY
Tr
LATTICE
TEMPERATURE Tj
Fig. 6. Entropy vs. temperature curve for a low-temperature paramagnet (schematic).
level is 1 erg per second, enough to
bring a cup of water to the boil in 25,000
years or boil it all away in 200,000 years!
The constraint which brings about the
fall in entropy at very low temperatures
is the interaction between the atomic
moments themselves. This may be
thought of as an equivalent molecular
field, h. Considering, again, the system
in terms of its entropy, we have
Initial conditions S, = f(uwH/kT;)
Final conditions S; ~ f(uh/kT;)
and, equating these (constant entropy
process),
HH ph
kik? OKT,
or
ili h
TH
This analysis, which is very approxi-
mate, gives one a fair estimate of the
T; to be expected using a starting field,
H, up to about 20,000 gauss. Internal
molecular fields are usually of the order
126
of 100 gauss and set a practical low
temperature limit of about 1 mK.
Nuclear Cooling
Atomic nuclei also possess magnetic
moments but about 1000 times smaller
than the electronic moments we have
been discussing up to this point. Their
interaction is very feeble indeed: a typical
‘‘internal field’’ is of the order of 1 gauss,
and the steep entropy drop (Fig. 6)
should occur in the neighborhood of
10-7 K. Unfortunately, this nuclear
magnetism is difficult to utilize effectively.
One needs a very intense magnetic field,
or a very low initial temperature, T;, or
some compromise combination in order
to achieve the requisite large value of
H/T.
In practice, these considerations have
necessitated employment of a 2-stage
process, again reminiscent of the gas
liquefaction process. Using such an
approach, Kurti and colleagues carried
out, at the Clarendon Laboratory in 1956,
the first nuclear cooling experiment. The
working substance was metallic copper
and the copper nuclei were cooled to
about 10~° K. Today, twenty years later
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
eee
and after numerous undertakings in
several laboratories, it is fair to conclude
that major operational difficulties still lie
in the way of applying such refrigera-
tion to extend scientific investigations.
By now we have lost sight of liquid
helium itself, so let us return to say a
few words about its own remarkable
properties.
Superfluidity
Highly startling properties set in at
2.2K for liquid helium, although 20 years
of continual usage followed the first
production in 1908 before they began to
be noticed! All appearance of boiling
ceases. The specific heat shows a very
sharp maximum. Density and dielectric
constant each shows a maximum. The
liquid becomes a fantastically good con-
ductor of heat. The liquid exhibits super-
fluidity, i.e., it spreads unrestrainedly
Over surfaces and cannot be contained in
a vessel unless the latter’s walls extend
into a region of temperature above 2.2K;
it will leak without evident impediment
through passages as small as micropores
in special glass (diameter ~107* cm).
The surface mobility occurs through
what came to be termed the creeping film
or Rollin film (after its discoverer). It
was this phenomenon which had be-
devilled Kamerlingh Onnes’ attempts to
force-evaporate liquid helium below a
temperature of 0.7K. We also now know
that solid helium cannot exist at pressures
less than 25 bar.
The peculiar properties of liquid helium
mentioned above, plus many related un-
usual phenomena, opened up an enormous
area of research which is still under
study today in many laboratories through-
out the world. It is,however, a difficult
subject to say just a little about and I now
therefore set it aside.
Nuclear Orientation
This is closely allied to the subject
of nuclear cooling. The spatial orientation
of nuclei is only the first stage in the
latter process, but it is of intrinsic
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
interest if the nuclei are radioactive. The
emitting nuclei are like little radio an-
tennae and, similarly, the emissions have
directional characteristics, the precise
features of which depend on nuclear
physics details. At ‘‘high’’ temperatures,
all these directional effects are smeared
out. ,
In order to interpret the emission
pattern, one needs to know the facts
concerning two out of the three of the
nuclear physics, the solid state physics,
and the temperature. Hence three en-
tirely distinct fields of research are avail-
able here. The most famous nuclear
physics research was the demonstration
of parity-nonconservation in beta decay,
at NBS in 1956. Also made possible is
a very useful thermometer, the merits of
which are now becoming widely recog-
nized.
Thermometry
Thermometry in low temperature re-
search is important and, as might be
anticipated from the remarks just con-
cluded, highly specialized. In addition to
the anisotropic-gamma-emission-from-
oriented-nuclei thermometer already
mentioned, several different kinds are in
use, a choice always having to be made
to best fit the experimental circum-
stances. Commonest are the magnetic
thermometer, employing paramagnetic
susceptibility and sometimes (where the
approximation suffices) assuming the
Curie Law for simplicity; and certain
kinds of resistance thermometer, both
metallic and semiconducting types. And
just recently, as the new superconducting
measurement technology has made pos-
sible greatly enhanced sensitivity for the
measurement of (among other properties)
magnetic susceptibility, so we may now
use the nuclear magnetic susceptibility
for a temperature indication.
The y-ray thermometer indicates
temperature by our relying on a knowl-
edge of physics and constants of nature;
it is therefore a primary thermometer.
Other low-temperature sensors in this
category are the acoustic (speed of sound
127
in helium gas) thermometer, though this
is not suitable for temperatures below
2K, and a low temperature version of the
Johnson noise thermometer invented by
Kamper. These two devices are playing
their part in establishing a temperature
scale for the cryogenic region but they
are not suitable as practical thermome-
ters for use in everyday experimental
application.
A part of this scale-development work
entails accurately determining the tem-
perature of sharply-defined physical phe-
nomena for use as thermometric fixed
points, so that reliable temperature
references are available for all laboratories
which have such a need. To this end,
NBS is developing superconducting fixed
points which make use of the steep fall
to zero of the electrical resistance of
certain metals, as described above with
reference to Kamerlingh Onnes pioneer-
ing discovery. At present, pure metal
superconductors are available covering
the range from 15 mK (tungsten) to
7K (lead) and others are under investiga-
tion which, it is hoped, will soon extend
the range up to about 20K.
Superconductivity in General
In the late 1940’s and early 1950’s,
theoretical ideas on the origins of super-
conductivity began to take shape. The
early work of Frohlich and Bardeen
led in 1957 to the Bardeen-Cooper-
Schrieffer (BCS) theory which for the
first time gave a Satisfactory, micro-
scopic explanation of the basic phe-
nomenon. In the mid-1950’s, too, Russian
physicists, notably Landau and Ginsburg
and, subsequently, Abrikosov and Gor-
kov, concentrated theoretical efforts on
the inhomogeneous features of the super-
conducting state and thence predicted
the possibility of a new class of super-
conductors. :
The theoretically-anticipated ‘‘Type II
superconductors’” appeared on the ex-
perimental scene around 1960. Their
dominant features are an ability to handle
high current densities and to withstand
intense magnetic fields. Electromagnets
128
producing fields of 100,000 gauss and
more were built and today these are
readily available commercially. [Com-
parable conventional electromagnets have
also been built during the last 25 years
but these require several megawatts of
electric power and vast cooling arrange-
ments. Superconducting magnets, on the
other hand, require no continuous power;
a circulating current, once initiated, will
flow as long as the liquid helium lasts].
Research is being pursued for alloys or
compounds which show superconduc--
tivity up to even higher temperatures.
Transition temperatures higher than 20K
have been achieved, but only in systems
which, for the moment, have to be
classified as laboratory curiosities.
In 1962, Josephson developed the
theory of the weak-link superconducting
circuit, for which work he subsequently
received the Nobel prize. Experimenta-
lists almost ignored the subject for a year
or two, whereafter took place a very
rapid build-up of related research and
development of devices in the world’s
cryogenic laboratories. The basic equa-
tion }
j = Josin 6
is, with only a modicum of exaggera-
tion, reminiscent of E = mc? in that it
is ludricously simple in appearance,
summarizes a wealth of physics impos-
sible to explain in a mere couple of
sentences, and leads to quite extra-
ordinary practical consequences. Making
an artifact out of the basic idea led to
something termed a Superconducting
Quantum Interference Device, or SQUID,
which is also ludicrously simple in
essence. Already, this type of device has
been employed to develop a) a new
international standard for the volt, b) a
new primary low temperature thermome-
ter (above), c) voltage, current, and
magnetic field measuring devices of
extraordinary sensitivity, not least of
which is d) a magnetocardiograph.
This superficial, rapid and perhaps
bewildering romp through 100 years of
endeavour will not be complete without
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
a gg een nerds
33
d
32
a
eS
= 3!
<
Q=
30
29
Ore Ol, OSE BOS cy NO4). OF. 06: OF,
T( K)
Fig. 7. Melting pressure of *He vs. temperature (after R. A. Scribner, M. F. Panczyk,
ind E. D. Adams, J. Low Temp. Phys. 1, 313 [1969}).
a word or two about industrial applica-
tions and at least a nod in the direction
of the light isotope of helium.
3He
This rare substance, of relative (to
*He) abundance 10°° in atmospheric
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
helium and 1077 in oil-well helium, has
recently become available to researchers
in quite generous quantity thanks to the
nuclear weapons industry. When com-
pared with its heavier relative, it has
quite different bulk properties. These are
of great intrinsic interest to the scientist
129
while some, in particular, have con-
siderable practical importance in cryo-
genic research.
First, when lowered in temperature
below 0.3K, the melting curve (Fig. 7)
passes through a minimum and rises
again. This results in a correspondingly
unusual entropy behavior, and one finds
that compressing the liquid isentropically
causes a cooling (called Pomeranchuk
cooling after the inventor). A tempera-
ture of 1 mK has been reached in this
way; the method entails compression to
30 atmospheres.
Second, in the liquid state >He—*He
mixtures separate into 2 phases at very
low temperatures, the one richer in *He
being uppermost. By forced evaporation
one may disturb the equilibrium and cause
3He atoms to move accross the phase
boundary. The process is analogous to
volume expansion and the temperature
falls, a refrigeration process first en-
visaged by H. London in 1951 and put
into practice by him and co-workers in
1962. From about 1966 on, the pace of
development picked up rapidly and soon
commercial versions became available.
With such equipment the cryophysicist
can now have at his disposal continuous
refrigeration for the millikelvin region,
a most important research tool. Recent
advances in this area include the dis-
covery of superfluidity in liquid *He at
2 mK (contrast this with the transition
in *He at 2.2K).
Industrial Developments
A few items, briefly mentioned, will
serve to impress one with the giant
strides made in cryotechnology over the
past century, most of them coming in the
130
last decade or two. Today in the United
States, there is a $300M annual produc-
tion of liquid oxygen, 50% for the steel
industry and 20% in the chemical
industry. Annual sales of liquid nitrogen
are about $150M with more than one-
third used for freezing food. By 1985,
about 10% of our natural gas will be
imported in the liquid state. This activity
requires the provision of very large
storage tanks, some 10 stories high!
Liquid hydrogen is used as a fuel in space
rockets (it is also being tested for an
alternative to gasoline in automobiles)
and is stored in containers of 1 million
gallons capacity. The U.S. Navy is build-
ing 3000 H.P. superconductive motors
and generators and has design work
under way for 30,000 H.P. Supercon-
ductive cable for power transmission is
being developed, and Japan has a super-
conductive motor-driven and levitated
train.
Helium is even exported today in the
liquid state, 6000 gallons at a time by
ocean transport. This brings me to end
on a pessimistic note: for decades helium ~
was just allowed to escape into the
atmosphere; then for a time it was
separated from the natural gas and re-
stored underground; a few years ago this
federally-sponsored program was. ter-
minated in an economy move. It is there-
fore possible that just as this country
is prepared to move forward into a major
national exploitation of low temperature
technology we shall reap our reward for
the profligate waste of this precious,
irreplaceable resource that has been
going on for many decades, i.e., we shall
run out of helium. But that is another
entire lecture!
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
Polynomial Regression Analysis Using a Principal
Components Rotation
Richard H. McCuen
Associate Professor, Department of Civil Engineering,
University of Maryland, College Park, Md. 20742
ABSTRACT
Fitting nonlinear relationships using a polynomial calibrated with multiple regression
usually leads to irrational coefficients. However, by using a principal components
rotation of the correlation matrix prior to regression, a set of rational coefficients may
be obtained for polynomials. An analysis of daily pan evaporation and mean air tempera-
ture is used to illustrate the value of fitting polynomials using a_ principal
components analysis.
Regression techniques are used for pre-
diction in engineering and the physical
sciences as well as in the behavioral
sciences. While linear regression is the
most frequently used technique, bi-
variate relationships that exhibit non-
linear trends are not uncommon. For
nonlinear relationships, the least squares
criterion is frequently used to obtain
a polynomial equation to represent the
relationship between the two random
variables.
The method of regression that is used in
polynomial analyses makes the critical as-
sumption that the variables used for pre-
diction are independent. In polynomial
analyses the predictor (independent)
variable and powers of it are used as the
predictors. But the predictor variable and
its powers are never independent and
they are usually very highly correlated.
This violates the basic assumption of the
least squares criterion and often results
in irrational coefficients in the polynomial
equation. The irrational coefficients often
result in irrational predictions, especially
for values of the predictor variable that
are outside the range of the data used
for calibrating the polynomial.
This paper presents a technique that
circumvents the intercorrelation problem
without an appreciable loss in accuracy
of prediction. The calibration algorithm
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
is based on a principal components
rotation of the correlation matrix. By
circumventing the intercorrelation prob-
lem, a polynomial with rational coef-
ficients can be obtained.
Eigenstructure Analysis
The least squares solution for poly-
nomial analysis requires the inversion of
the correlation matrix. When high inter-
correlation exists between the predictor
variable and powers of it, then the
correlation matrix may be singular or
near-singular. In such cases, the ac-
cumulation of round-off error becomes
appreciable and irrational coefficients
are the result.
Principal components analysis pro-
vides an alternative solution. By rotating
the correlation matrix prior to using the
least squares criterion, a set of orthogonal
vectors that can be used to obtain the
regression coefficients are provided. The
orthogonal vectors are obtained using a
principal components analysis of the cor-
relation matrix.
A principal components analysis of a
correlation matrix R is based on the
solution of the simultaneous equations,
expressed in matrix form as:
RV =)V (1)
131
where R is an (n X n) matrix of bivariate
correlation coefficients, V is a (n xX 1)
vector of unknowns, and AJ is a scalar.
A solution of equation 1 provides values
for the constant A, which is called the
eigenvalue, and the vector V, which is
the eigenvector. For a matrix R of rank
m (m = n) there will be m solutions to
equation 1. The resulting eigenvalues and
eigenvectors represent the eigenstructure
of the correlation matrix.
While a geometric interpretation of
the eigenstructure analysis is informative
(Cooley and Lohnes, 1971), it may suffice
here to provide interpretations of the
eigenvalues. The eigenvalue divided by
the rank of the matrix represents the
proportion of variance in the correlation
matrix that is extracted by the cor-
responding principal component. Be-
cause not all of the variance is meaningful
(i.e., a portion of the variance represents
random error), not all of the eigenvalues
and eigenvectors are statistically signif-
icant. A regression analysis that is
based only on the significant eigenvalues
and eigenvectors will usually produce a
rational prediction model. By eliminating
the unwanted random or error variance,
the coefficients will remain rational.
While many criteria have been pro-
posed for identifying the significant
eigenvalues, Kaiser’s rule-of-thumb
(Kaiser, 1960) is generally recognized as
the most reliable. Kaiser’s rule states
that for samples of small or moderate
size, all eigenvalues greater than one are
Statistically significant.
Polynomial Analysis with Principal Components
A computer program was developed
that permitted the calibration of poly-
nomials using a regression based on a
principal components analysis of the cor-
relation matrix. While the criterion
variable is regressed on a linear function
of the principal components rather than
the predictor variable and its powers, the
resulting prediction equation does not re-
quire the evaluation of the eigenstructure
when determining a predicted value of the
criterion variable.
132
The solution is an iterative process in
which a prediction equation is calibrated
for the analysis based on the sequential
addition of eigenvalues. And because
some of the variation in the correlation
matrix is considered to be error varia-
tion, the total explained variation (i.e.,
the square of the correlation coefficient)
for the principal components model may
be smaller than that explained by the
polynomial model calibrated using the
standard regression analysis technique.
The method will be illustrated using a
data set that consists of the daily pan
evaporation (inches/day) and the average
daily air temperature (°F). Three hundred
fifty-four observations were obtained
from a site near Tifton, Ga. The following
linear regression equation was derived:
E, = —.114 + 0.00383T (2)
where E is the pan evaporation in
inches per day, and T is the daily mean
air temperature (°F). The equation pro-
vided a correlation coefficient of 0.581.
Table 1 gives predicted values of evapora-
tion for selected values of T. While
the true values are not known, the esti-
mate for a temperature of 100°F was
considered to be about 10% low; other-
wise, the model provides reasonably
good estimates.
Using the multiple regression tech-
nique with temperature and its powers
as predictor variables, the following
quadratic and cubic polynomials were
evaluated:
E, = 0.425 — 0.0142T + .000143T? (3)
and
E, = —0.239 + 0.0205T
— 0.000439T? + 0.00000314T? (4)
Equations 3 and 4 resulted in correla-
tion coefficients of 0.648 and 0.654,
respectively. These represent an increase
in the explained variation of approximately
8% and 9%, respectively, in comparison
with the linear model. The computed
values of Table 1 and the graphical
representation of the equations in Fig. 1
indicate that the models are not rational.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
Table 1.—Predicted Values of Pan Evaporation for Selected Air Temperatures.
Predicted pan evaporation (inches/day) with:
Linear
Temperature (°F) model
32 .009
50 .078
His US)
100 .269
Both models have irrational values at
temperatures of 32° F and at 100° F.
Furthermore, the quadratic equation
shows a noticeable downward trend that
extends even above temperatures of
50° F, which is within the range of the
data used for calibrating the models.
Thus, the nonlinear models are not
rational when calibrated using polynomial
fitting with multiple regression, which
is the traditional method of analysis.
A cubic equation was calibrated using
the polynomial analysis with a principal
components rotation of the correlation
matrix. The eigenstructure analysis re-
sulted in 3 eigenvalues, with the first
eigenvalue equal to 2.981 and each of the
other 2 eigenvalues less than 0.015. Thus,
according to Kaiser’s rule-of-thumb there
is only 1 significant eigenvalue and eigen-
vector. The cubic polynomial resulting
from a regression on this eigenvector
produced the following equation:
E, = —0.0324 + 0.00134T
+ 0.0000106T? + 0.00000011T? (5)
A correlation coefficient of 0.607 re-
sulted. This is noticeably larger than that
for the linear model and only slightly
less than those for the quadratic and cubic
equations derived from multiple regres-
sion. However, equation 5 provides more
rational predictions than any of the equa-
tions derived using the traditional method
of analysis. ©
While only 1 eigenvalue was found to
be significant, this represented 99.4%
(2.981/3) of the variation in the correla-
tion matrix. The remaining 0.6% of the
variation is considered to be error varia-
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
Principal
Quadratic Cubic components
model model model
ot 7 .070 .025
.073 081 .075
.164 .154 .174
.435 561 S17
tion. But by including this in the analysis,
the irrational model of equation 4 results.
By eliminating this error variation, equa-
tion 5 produced more rational estimates.
Discussion and Conclusions
Nonlinear trends are often identified in
data sets from many physical systems.
Such nonlinearity may result because of
nonlinear processes that govern the
response of the system or because of the
large variation in the data used to
establish the relationship and the change
in the importance of the various processes
within the system. Many researchers have
attempted to circumvent this nonlinearity
by transforming the data; a logarithmic
transformation is very common. However,
principal components model
.60 — — linear model
quadratic model
i Cuptlcemoded /
Lake Evaporation (inches/day)
Air Temperature (°F)
Fig. 1.—Comparison of prediction models.
133
data transformations results in the violation
of theoretical considerations that form
the basis for the regression technique.
Specifically, when data are transformed
the distribution of the residuals is rarely
normal. Thus, polynomial fitting using a
principal components rotation provides
an alternative to data transformations.
Model selection from among alterna-
tives is often based on statistical criteria;
for example, the model producing the
highest correlation coefficient is often
selected. While statistical criteria, such
as the goodness-of-fit criteria of the cor-
relation coefficient and the standard error
of estimate, are useful indices of the fit
between observed and predicted values,
they may not be a reliable index for
the accuracy of future predictions with
the model, especially when the sample
size 1s small. Thus, criteria other than
134
Statistical goodness-of-fit criteria are just
as important, and probably more im-
portant. The rationality of the coefficients
and the distribution of the errors are two
criteria that should always be assessed
when developing a model. The regression
technique that includes a principal com-
ponent rotation appears to provide
rational coefficients for N™ order poly-
nomials and thus is a valid alternative to
the frequently used multiple regression
technique for polynomial analyses.
References Cited
Cooley, W. W., and P. R. Lohnes. 1971. Multi-
variate Data Analysis, John Wiley and Sons, Inc.,
New York.
Kaiser, H. F. 1960. Comments on Commonalities
and the Number of Factors. Read at an informal
conference, ‘‘The Communality Problem in
Factor Analysis,’ St. Louis: Washington Uni-
versity (dittoed).
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
RESEARCH REPORTS
Microcracking of Concrete
K. N. Derucher
Department of Civil Engineering, University of Maryland,
College Park, Maryland 20742
ABSTRACT
The major objective of this investigation was to directly observe the formation
and/or propagation of microcracks in concrete both before and after application of
compressive stress fields.
Concrete, under compression, fails when microcracks have propagated to the extent
that the concrete will not support the applied loads. Many investigators have implied
that the failure mechanism of concrete is related to internal microcracking. However,
due to the limitations in the techniques employed, the detection of microcracks was
somewhat uncertain.
The scanning electron microscope (SEM) was chosen as the viewing apparatus because
of its distinct advantages to directly observe the formation and/or propagation of
microcracks.
Microcracks were found to exist in concrete prior to application of compressive
stress fields in the form of shrinkage microcracks (initial bond microcracks). As
the compressive stress field is increased, these microcracks wide and propagate until
failure occurs.
Many investigators have implied that
the failure mechanism of concrete is
associated with internal microcracking
(1-6). The formation and propagation
of such microcracks have been studied
indirectly by sonic velocity, acoustic
methods, and by the observation of
macrocracks on the surface of the
models. Robinson (7) and Hsu et al. (8)
have directly observed the formation and
propagation of microcracks by x-ray
analysis. Due to the limitations in the
technique employed, the detection of
microcracks was somewhat uncertain.
In addition, Hsu et al. used a light
microscope at 40x magnification to
verify the results of the x-ray analysis.
They examined cross sections of con-
crete (0.15 inches thick) both before and
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
after application of compressive stress
fields. In those concrete models which
were examined after application of com-
pressive stress fields, the concrete was
sliced perpendicular to the direction of
the applied load. Prior to slicing and
examination of the concrete models, they
were subjected to various compressive
stress fields and the loads were subse-
quently removed.
According to Hsu et al., 3 types of
microcracks were identified: bond, ma-
trix, and aggregate microcracks. Further,
bond microcracks (microcracks between
the cement mortar matrix and aggregate
particles) exist in the form of shrinkage
microcracks prior to application of com-
pressive stress fields. These initial micro-
cracks begin to propagate at approxi-
135
mately 30—40% of the ultimate strength.
The stress-strain curve deviates from
linearity at this point, and there is an
increase in the lateral expansion of the
concrete. Matrix microcracks (micro-
cracks in the cement mortar matrix) are
formed by propagating bond micro-
cracks at about 70-90% of the ultimate
strength. Aggregate microcracks occur
just before failure.
Hansen (9), in an attempt to verify
the conclusions of Hsu et al., disagreed
on some aspects of their findings. Hansen
also tried to observe microcracks in
concrete both before and after applica-
tion of compressive stress fields, but the
compressive stress fields were not re-
moved prior to observation. Hansen ap-
plied a purely axial compressive stress
field to the concrete models and observed
(using a light microscope at 50X mag-
nification) the formation and propagation
of surface microcracks. Under a purely
axial load, microcracks are believed to
originate in the center of the concrete
and propagate to the outer surface.
Hansen, however, did not find bond
microcracks in the form of shrinkage
microcracks prior to application of
compressive stress fields under magni-
fications as high as 1000 with the light
microscope. Hansen discovered that
bond microcracks (under a magnification
of 50x) occurred at about 45% of the
ultimate strength unlike the 30-40%
figure found by Hsu et al. He agreed
that matrix microcracks occur between
70 and 90% of the ultimate strength, and
that aggregate microcracks occur just
before failure.
It is apparent from the differences
Table 1.— Parameters considered.
Parameters
Ultimate Strength
Coarse Aggregate Shape
Fine Aggregate Shape
Top Size of Coarse Aggregate
Curing Time
Curing Temperature
Curing Relative Humidity 29 + 2%
Number of Samples 4
Rounded
Rounded
28 days
136
Model 1
3000 Ibs/in? (211 kg/cm?)
0.50 in. (1.27 cm)
70°F (21°C)
in the data received and the techniques
employed by Hsu et al. and Hansen that
further basic research is needed in the
field of concrete microcracking. A better
understanding of the failure mechanism
of concrete (at the microlevel) may pro-
vide a more knowledgeable understand-
ing of the engineering properties of
concrete, possibly leading to develop-
ments for improving these properties and
subsequently improved use of concrete
materials.
The major objective of this investiga-
tion was to observe directly the forma-
tion and/or propagation of microcracks
in concrete both before and after the
application of compressive stress fields.
The compressive stress fields selected
were 15, 45, and 75% of the ultimate
strength of concrete.
It was not known what effect, if any,
aggregate shape would have on the
formation and/or propagation of micro-
cracks in concrete. As a result, 2
distinct concrete models were used with
the following parameters (Table 1).
Design of Experimental Investigation
It was decided to use the scanning
electron microscope (SEM), model AMR
900 as the viewing apparatus (to observe
microcracks in concrete directly) be-
cause of its unique capabilities and its
distinct advantages over other viewing
apparatus such as the light microscope
and the transmission electron micro-
scope. With the SEM it is possible to
scan a 1 in? area, to magnify the same
area 100,000, and to obtain a relatively
clear, sharp photograph.
Model 2
3000 Ibs/in? (211 kg/cm?)
Angular
Angular
0.50 in. (1.27 cm)
28 days
70°F (21°C)
98 + 2%
4
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
(a) Ix 2-1/8"x 1/8" BRASS PLATE (F) 2"x 4"x I" CONCRETE MODEL
@
~
Pa)
no (yt
ii Na
I"x 1" VIEWING AREA
() I"x 3-3/4" 3/8" STEEL PLATE (x) 1/8" STEEL ROD
(0) LUBRICATED O-RINGS
() 1/2" DIAMETER STEEL BOLT
(6) SR-4 STRAIN GAGES
C) TEFLON SHEET
p
P = CONCENTRATED LINE LOAD
e = ECCENTRICITY VALUE
SECTION A-A
Fig. 1. Loading apparatus.
Two SEM limitations were encountered
in this type of investigation. First, there
mas only a 5S’ x 7” x 1-44" (12.7 cm.
x 17.8 cm. X 3.8 cm.) usable space in
the high-vacuum (10°° torr) chamber.
Since the major objective of this in-
vestigation was to observe microcracks
directly in concrete under application of
compressive stress fields, a loading ap-
paratus (Fig. 1) had to be designed which
would allow for the maximum size model
possible (Fig. 2) and still be placed in
the SEM vacuum-chamber in its entirety.
The loading apparatus had to be designed
to allow for the direct observation of
microcracks when they form and/or
propagate; this necessitated the eccentric
loading of the concrete models. Thus, the
size of the SEM vacuum-chamber con-
trolled the size of the loading apparatus
as well as the size of the concrete
models.
The second limitation of the SEM was
that in a high vacuum the concrete models
must be relatively free of moisture; other-
wise, due to the moisture in the concrete
models, optimum operation cannot be
reached. The models may contain molec-
ular moisture; any moisture in excess
of this amount cannot be tolerated. This
limitation required developing a delicate
4-cycle drying process that would not
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
include microcracking. The 4-cycle dry-
ing process consisted of: air drying,
desiccator drying (with silica gel as the
desicant), vacuum-desiccator drying, and
oven drying. In each cycle the models
were dried to constant weight (as deter-
mined by daily weighing) before ad-
vancing to the next cycle. The entire
process lasted approximately 25 days. To
ou
fs |
EWA
é
Fig. 2. Concrete shape and size (Model).
7A
137
Fig. 3 (top left), shrinkage microcrack prior to application of 4-cycle drying process.
Fig. 4 (middle left), shrinkage microcrack after application of 4-cycle drying process.
Fig. 5 (bottom left), scanning area of the concrete model containing rounded aggregate.
Fig. 6 (top right), scanning area shown in Fig. 4 magnified to illustrate existence of shrinkage micro-
cracks in concrete containing rounded aggregate.
Fig. 7 (middle right), microcracks in concrete containing rounded aggregate under application of a
compressive stress field of 15% of the ultimate strength.
Fig. 8 (bottom right), microcracks in concrete containing rounded aggregate under application of a
compressive stress field of 45% of the ultimate strength.
confirm the fact that the drying process Results
would not induce microcracking, a pro- Shrinkage Microcracks.—The results
cedure was established with the use of indicate the existence of shrinkage mi-
the light microscope. crocracks both in concrete containing
138 J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
Fig. 9 (top left), scanning area of the concrete model containing angular aggregate.
Fig. 10 (middle left), scanning area shown in Fig. 8 magnified to illustrate existence of shrinkage
microcracks in concrete containing angular aggregate.
Fig. 11 (top right), microcracks in concrete containing angular aggregate under application of a com-
pressive stress field of 15% of the ultimate strength.
Fig. 12 (middle right), microcracks in concrete containing angular aggregate under application of a
compressive stress field of 45% of the ultimate strength.
Fig. 13 (bottom), microcracks in concrete containing angular aggregate under application of a com-
pressive stress field of 75% of the ultimate strength.
rounded aggregate and in concrete con- propagated, or widened these shrinkage
taining angular aggregate. Neither the microcracks. Many shrinkage micro-
delicate 4-cycle drying process nor the cracks were encountered in the concrete
SEM in obtaining a high-vacuum created, models, though only a few photographs
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977 139
will be shown. Fig. 3, obtained with the
light microscope at an original magni-
fication of 200, is a typical shrinkage
microcrack, in concrete containing
rounded aggregate, prior to the applica-
tion of the 4-cycle drying process.
Similar shrinkage microcracks were en-
countered in concrete containing angular
aggregate. These shrinkage microcracks
are known as initial bond microcracks.
It was concluded from Fig. 3 and similar
photographs that microcracks exist in
concrete prior to application of compres-
sive stress fields.
Fig. 4, also obtained with the light
microscope at an original magnification of
200, is the same shrinkage microcrack
shown in Fig. 3, but after the 4-cycle
drying process. In a comparison of Figs.
3 and 4, there do not appear to be any
differences, nor was there any change in
the existing microcracks or development
of new ones. As a result, it was con-
cluded that the 4-cycle drying process did
not create, propagate, or widen shrinkage
microcracks.
Microcracks in Concrete Containing
Rounded Aggregate .—Figs. 5 through 8
are photographs of microcracks obtained
with the SEM in concrete containing
rounded aggregate both before and
after application of compressive stress
fields. Fig. 5 is a photograph of the
scanning area of the concrete model prior
to application of compressive stress
fields: shrinkage microcracks are not
obvious at this magnification. By mag-
nifying and photographing the encircled
area, Fig. 6 is obtained.
It is apparent from viewing Fig. 6 that
shrinkage microcracks exist in concrete
containing rounded aggregate. This
shrinkage microcrack is not merely an
initial bond microcrack (as described by
Hsu et al.) but has matrix microcrack
extensions. The average width of the
microcrack in Fig. 6 is approximately
3 microns.
Applying a compressive stress field of
15% of the ultimate strength, a value
within the straight line portion of the
stress-strain curve, and viewing the en-
circled areas of Fig. 6 results in Fig. 7.
140
It would appear that the microcracks
have doubled in size (6 microns) and the
matrix microcrack in the upper right hand
corner of Fig. 6 has propagated.
By increasing the compressive stress
field further to 45% of the ultimate
strength and viewing the same area as in
Figs. 6 and 7 results in Fig. 8. The
microcracks have widened considerably,
approximately 8 times (21 microns) their
original width.
Microcracks in Concrete Containing
Angular Aggregate. — Figs. 9 through 13
are photographs of microcracks, observed
with the SEM, in concrete containing
augular aggregate both before and after
application of compressive stress fields.
Fig. 9 is a photograph of the scanning
area of the concrete model prior to ap-
plication of compressive stress fields.
Again shrinkage microcracks are not ob-
vious at such a low magnification.
However, if the encircled area is mag-
nified and photographed, Fig. 10 results.
It is obvious, from viewing Fig. 10, that
shrinkage microcracks exist in concrete
containing angular aggregate. This shrink-
age microcrack is not merely an -initial
bond microcrack (as described by Hsu
et al.) but deviates from the aggregate-
matrix interface (bond) into the matrix.
The average width of the microcrack in
Fig. 10 is approximately 2 microns.
Applying a compressive stress field of
15% of the ultimate strength and viewing
the encircled area of Fig. 10 yields Fig.
11. The bond portion of the microcrack
has increased in width approximately
5 times and the matrix microcrack
extensions have become much more pro-
nounced.
Increasing the compressive stress field
to 45% of the ultimate strength and
viewing the same encircled area as in
Figs. 10 and 11 results in Fig. 12. At
this point, matrix microcracks begin to
bridge bond microcracks with no notice-
able increase in width, and the matrix
microcracks become much more pro-
nounced.
With a further increase of the com-
pressive stress field to 75% of the ultimate
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
strength, Fig. 13 results. There appears
to have been a shifting of the aggregate
particle and a widening of the microcrack.
Discussion of the Results
Shrinkage Microcracks.—This_in-
vestigation supports the results of Hsu,
Slate, Sturman, and Winter in their study
of shrinkage microcracks: microcracks
exist in concrete prior to application of
compressive stress fields. The results
further show that shrinkage microcracks
exist both in concrete containing rounded
ageregate and in concrete containing
angular aggregate. These shrinkage mi-
crocracks were not just initial bond
microcrack extensions at right angles.
Sturman (10) suggested that shrinkage
microcracks may be formed by variety of
processes, including carbonation shrink-
age, hydration shrinkage, segregation
due to settlement, and drying shrinkage.
It is hypothesized that the shrinkage
microcracks encountered in this in-
vestigation resulted from segregation due
to settlement and, to some extent,
hydration shrinkage.
Carbonation shrinkage occurs when
any cement compound is stored in air
and decomposed by carbon dioxide. The
portland cement used in this investigation
was of good quality and had just been
manufactured and purchased. It had very
little time to be exposed to air. Therefore,
it does not seem likely that shrinkage
microcracks were formed by carbonation
shrinkage.
Hydration shrinkage occurs when the
primary cement-paste volume decreases
its volume during hydration, resulting in
the formation of microcracks. This is said
to be controlled by expansive cements.
Since Type III-A cement (used in this
investigation) is not an expansive cement,
microcracks are possible.
According to Sturman, the influence of
segregation due to settlement on the
formation of microcracks may be analyzed
by applying Stoke’s law to the viscous
material first formed when sand, cement,
and water are mixed to form mortar.
Stokes found that for very small solid
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
particles suspended in a viscous fluid,
the steady state or terminal velocity
acquired by the larger and denser
particles is greater than that of the
smaller, less dense particles. Thus, in the
sand-cement-water mixture the large
sand particles will settle first, the fines
next, and the extremely fine, flocculated
particles last. This leads to a condition
in which there is, adjacent to the ag-
gregate, a thin film of fluid with an
extremely high water to solids ratio.
Eventually this water is absorbed by
the adjoining cement paste which hy-
drates continuously and a thin space is
left at this point on the aggregate.
When this sedimentation occurs at the
exposed horizontal surface of freshly
poured concrete, it is referred to as
bleeding. This phenomenon is likely the
cause of shrinkage microcracks in con-
crete and is probably the major cause
of shrinkage microcracks in this in-
vestigation.
The final possibility is drying shrink-
age. Drying shrinkage occurs in plastic
concrete if the rate of evaporation ex-
ceeds 0.1 Ibs/ft.? of surface area/hr. In
other words, hydrostatic tension is
present, resulting in shrinkage micro-
cracks. If the concrete were cured in a
water-saturated atmosphere, as it was in
this investigation, shrinkage microcracks
do not develop. Therefore, this possibility
was ruled out.
It was not known why Hansen did not
encounter shrinkage microcracks, be-
cause there was no information avail-
able as to the concrete materials and
curing procedures used.
Concrete Containing Rounded Ag-
gregate and Concrete Containing An-
gular Aggregate.—Hsu et al. stated that
bond microcracks (which exist prior to
the application of compressive stress
fields) propagated at 30-40% of the
ultimate strength. Hansen found that
bond microcracks did not originate un-
til 45% of the ultimate strength. In
this investigation, bond microcracks
(which exist prior to the application of
compressive stress fields) did not propa-
141
gate at all but merely widened under
increasing compressive stress fields. The
propagation of microcracks occurred
only to the matrix extensions.
Both Hsu et al. and Hansen further
agree that matrix microcracks occurred
between 70 and 90% of the ultimate
strength. In this investigation, matrix
microcracks were extensions of bond
microcracks and existed prior to appli-
cation of compressive stress fields. These
matrix microcracks were at right angles
to the bond microcracks. Under in-
creasing compressive stress fields (as
low as 15% of the ultimate strength)
matrix microcracks widen and propagate
to the point that they begin to bridge
bond microcracks.
This investigation further shows that
at 45% of the ultimate strength the
bridging of bond microcracks is about
completed. At 75% of the ultimate
strength the matrix microcracks start to
bridge one another.
The differences between the results
obtained in this investigation and those
of previous investigations are easily
explained. The depth of field and scan-
ning ability are the 2 features that make
the SEM particularly well suited for
fractography. Its depth of field is many
times greater than that provided by the
light microscope (such as that used by
Hsu et al. and Hansen) for equiva-
lent magnifications. This feature permits
both the peaks and valleys normally
encountered on rough fractured surfaces
to be imaged in focus, even at rela-
tively high magnifications. The light
microscope used in previous investiga-
tions had poor depth of field at 40X and
50X magnification. This poor depth made
it difficult to distinguish between ac-
tual microcracks in the matrix and very
porous mortar. Even the use of the
light microscope in this investigation
presented doubt as to the existence of
an actual microcrack. At lower com-
pressive stress fields Hsu et al. and
Hansen may have mistaken the micro-
cracks to be very porous mortar (since
the microcracks were only 3 or 4 microns
wide) and only when the microcracks
142
reached a proportional size could a differ-
ence be made. This may account in
part for the higher values received by Hsu
et al. and Hansen in their investiga-
tion of matrix microcracks.
In addition, Hsu et al. removed the
compressive stress fields prior to ob-
servation of microcracks. Many micro-
cracks which formed may have gone
unnoticed, because they may have closed
due to the relief in stress. Again, this
may account for in part the high values
received by Hsu et al.
In Hansen’s investigation, surface
microcracks were observed. Hansen ap-
plied a purely axial compressive stress
field to the concrete models. Under an
axial load microcracks are believed to
originate in the center of the concrete
models and then propagate to the outer
surface. Under this assumption, micro-
cracks would not be noticed on the
surface of the models until higher com-
pressive stress fields were reached. This
may account for the differences received
by Hsu et al. and Hansen as far as
bond microcracks are concerned.
Conclusions
The following are some of the con-
clusions drawn from this investigation:
1. Procedures, techniques, and appara-
tus were developed and/or modified
for the study of concrete fracture
utilizing the SEM.
2. Microcracks were found to exist in
concrete prior to application of com-
pressive stress fields. These initial
microcracks are shrinkage micro-
cracks. These shrinkage microcracks
were in the form of bond micro-
cracks (microcracks at the interface
between the aggregate and the matrix)
with matric microcrack extensions
(microcracks in the paste).
3. Shrinkage microcracks (initial bond
microcracks) propagate into the
matrix and widen under an increasing
compressive stress field. As the com-
pressive stress field approaches the
ultimate strength of concrete these
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
microcracks become macrocracks and
with time will fail the member.
4. Under increasing compressive stress
fields (as low as 15% of the ultimate
strength) matrix microcracks widen
and propagate to the point they begin
to bridge bond microcracks.
5. At 45% of the ultimate strength of
concrete the bridging of the bond
microcracks is about complete.
6. At 75% of the ultimate strength of
concrete the bridging of the matrix
microcracks begins and as the com-
pressive stress field is further in-
creased it is conjectured that these
microcracks will continue to widen
and propagate until failure occurs.
References Cited
(1) Brandtzaeg, A., ‘“‘Study of the Failure of
Concrete Under Combined Compressive
Stresses,’’ UIEES Bulletin No. 185, Novem-
ber 1928.
(2) Berg, O., “‘The Factors Controlling the
Strength of Concrete,’’ Constructional Re-
view, Vol. 33, No. 11, p. 19, November
1950.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
(3) Jones, R., ““A Method of Studying the Forma-
tion of Cracks in a Material Subjected to
Stress,’ British Journal of Applied Physics,
Vol. 3. p,, 229, 1952:
(4) L’Hermite, J., ‘“Present Day Ideas on Con-
crete Technology,’ 3rd Part, The Failure
of Concrete, Union of Testing and Re-
search Laboratories for Materials and Struc-
tures, Bulletin No. 18, pp. 27-39, June
1954.
(5) Hognestad, E., ‘“‘Concrete Stress Distribution
in Ultimate Strength Design,’’ Journal of
American Concrete Institute, Vol. 27, No. 4,
December 1955.
(6) Rusch, H., ‘‘Physical Problems in the Test-
ing of Concrete,’’ Cement-Chalk, V.12, No.
1, pp. 1-9, 1959.
(7) Robinson, J., ‘X-Ray Analysis of Concrete
Fracture,’ Journal of the American Concrete
Institute, Vol. 50, No. 8, Feb. 1959.
(3) Gosuya te... -Slate; .G. “Stugman, and .G.
Winter, ‘‘Microcracking of Plain Concrete
and the Shape of the Stress-Strain Curve,”’
Journal of the ACI, Vol. 60, No. 2, pp.
209-224, Feb. 1963.
(9) Hansen, T. C., ‘‘Microcracking of Concrete,”
Journal of the ACI, Vol. 64, No. 2, pp.
9-12, March 1968.
(10) Sturman, G., *‘Shrinkage Microcracks in Con-
crete,’ Ph.D. Dissertation, Cornell Univer-
sity, June 1969.
143
Prokopicrinidae, New Family of ?Camerate Crinoids,
Silurian (Wenlockian-Ludlovian), Tennessee
and Oklahoma
T. J. Frest and H. L. Strimple
Department of Geology, University of Iowa, Iowa City 52242
ABSTRACT
The new Silurian platycrinitacean crinoid genus Prokopicrinus represents an extreme
in calyx simplification among camerates. Perfectly pentamerously symmetrical aside
from the tripartite base, these diminutive (width 1.4—1.8 mm) monocyclic crinoids
lack interradials and anal plates or other indicators of the position of the anal opening
and can be oriented only by reference to the azygous basal (located in EA interray?).
The family Prokopicrinidae (nov.) probably are descended from the Hirneacrinidae,
culminating a trend in the superfamily Platycrinitacea toward expulsion of the inter-
radials (including the primanal) from the cup.
The Prokopicrinidae differ from the Hirneacrinidae and Hapalocrinidae in their
small size, and lack of both a differentiated CD interray and of interradials (IRR)
participating in the calyx; hence these crinoids cannot be assigned to existing
families. Parallel evolutionary trends in the inadunate orders Disparida (monocyclic;
microcrinoids and an undescribed hapalocrinitid) and Cladida (dicyclic; Elicrinus Prokop,
1973) produced similar-appearing genera; assignment of the family to the Camerata is
not indubitable.
Three new species are placed in Prokopicrinus: P. tuberculatus, the type species,
is a depressed bowl-shaped form with tumid plates, impressed plate sutures, and
irregularly developed tuberculate surface. P. laevis is characterized by a deeply bowIl-
shaped cup and smooth plates without impressed sutures. These 2 species are from
the Henryhouse Formation (Ludlovian), Oklahoma. P. barricki (Wenlockian; Waldron
Shale, Tennessee) has a basal flange, pentalobate calyx, and unevenly pitted
ornamentation (prosopon). All 3 were members of a sparse, relatively deep-water
crinoid assemblage typified by an abundance of Pisocrinus, Lecanocrinus and other
flexibles, calceocrinids, and microcrinoids. The small size of Prokopicrinus and
associated taxa, plus preservational factors, suggest a soft-bottom habitat with a slow
or moderate sedimentation rate and weak currents. The assemblage is possibly
analogous to the Dicoelosia-Skenidioides Community of Benthic Assemblage 4 of
Boucot (1975).
The echinoderm fauna of the classic
Waldron Shale (Wenlockian) localities
in Indiana has been fairly well known
for almost a century (Hall, 1879); not so
the echinoderms of equivalent strata in
Tennessee. An analogous situation ob-
tains for the Henryhouse Formation
(Ludlovian) of Oklahoma; the crinoids of
the typical facies were monographed by
Strimple (1963), but those from what we
interpret as a deeper water facies have
been neglected. Crinoids recovered re-
cently from some Waldron and Henry-
house shale samples are significantly
different from those of well-known locali-
144
ties. Common to both formations are
abundant pisocrinids and calceocrinids,
microcrinoids, and Lecanocrinus. Rare
are the large camerates normally quite
common in both. The Henryhouse
sample has abundant Gissocrinus; this
genus has not been found in the Waldron,
but small Stephanocrinus is exceedingly
abundant.
Brachiopods and ostracods are the
only other common invertebrate groups.
Fewer than the usual complement of
brachiopod genera are present; Dico-
elosia is quite abundant. Almost all the
crinoids and brachiopods are _ small;
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
many of the crinoids fall into the micro-
crinoid and minicrinoid (term defined
herein) size ranges, being less than 5 mm
in width. The crinoids described below
exemplify this observation; though fully
adult. none exceed 2 mm in diameter.
This has unfortunately precluded photo-
graphic illustration of the new taxa,
and camera lucida sketches are used
instead. Also hampering taxonomic treat-
ment is the rarity of complete calices
(isolated radials are common) and the
simple structure of many of the new
crinoids. Large-scale bulk processing has
not been attempted; though shaley, the
samples can be only partially disag-
gregated by standard procedures. No
crowns have yet been recovered, and
isolated skeletal elements are many
times more abundant than articulated
calices.
The extremely simple nature of the
calyx plate configuration of the crinoids
herein named Prokopicrinus makes it im-
possible to assign them unequivocably
even to subclass level. Nevertheless,
recent work on the early history of
the divergent camerate superfamilies
Patelliocrinacea and Platycrinitacea al-
lows placement of the new genus and
family in the latter with some confidence.
Well known phylogenetic trends within
the two superfamilies (Brower, 1973;
Frest and Strimple, 1977) reach their
apogee in the Prokopicrinidae; the exist-
ence of such forms could easily have
been predicted from previously known
information. Convergent evolution pro-
duced similar forms in the Inadunata at
about the same time; these crinoids
are, fortunately, not perfect homeo-
morphs of the Prokopicrinidae and can
be separated from the camerates on
‘various grounds.
All specimens have been placed in
the Repository, Department of Geology,
University of Iowa.
Systematic Descriptions
Class CRINOIDEA Miller, 1821
Subclass CAMERATA Wachsmuth
and Springer, 1885
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
Order DIPLOBATHRIDA Moore and
Laudon, 1943
Superfamily PLATYCRINITACEA Austin and
Austin, 1842
Diagnosis.—Calyx tending to be confined to
lowermost 2 plate circlets (patina); basals (BB) 3,
unequal (small one normally in AE interray) or
fused; brachials and interbrachials generally little
or not at all represented in calyx. Proximal
brachials tending to stand out clearly from radials
(RR) although joined firmly to calyx, tegmen, or
both by interradially situated plates in primitive
members; interradials absent in advanced mem-
bers; posterior side slightly or not differentiated
in calyx (adapted from Ubaghs, 1978).
Range.—U. Ordovician— Permian,
worldwide.
Included families.—Platycrinitidae
Austin and Austin, 1842; Hapalocrinidae
Jaekel, 1895; Hirneacrinidae Frest and
Strimple, 1977; Prokopicrinidae (nov.).
Remarks .—Our concept of the Platy-
crinitacea is essentially identical to that
promulgated by Ubaghs (1978) except
for a few points. We place the Mar-
supiocrinidae in the Patelliocrinacea,
rather than the Platycrinitacea; the ra-
tionale for our preference is given in
Frest and Strimple (1978). Addition of
the Hirneacrinidae and Prokopicrinidae
to the superfamily since Ubaghs’ work
was written necessitates minor emenda-
tion of his superfamilial diagnosis. The
additional two families represent the
culmination of certain phylogenetic trends
first recognized by Brower (1973) but
implicit in Ubaghs’ diagnosis within the
closely related Patelliocrinacea and Platy-
crinitacea. Most important is a tendency
to reduce the calyx to a patina of BB
and RR; concomitantly the IRR and
anals disappear or are expelled from the
calyx onto the tegmen, the arms may be-
come completely free at the RR, and near
perfect pentameral symmetry is achieved.
None of the half dozen Prokopicrinus
specimens thus far recovered preserve
the tegmen; this is analogous to the
situation in the Hirneacrinidae (Frest
and Strimple, 1977). Its lack of promi-
nence can be inferred readily from the
observation that the edges of the RR
extend onto the oral surface, covering
145
much) of it) (igs: 3) °6; 79). This’ ar-
rangement is also duplicated in the
Hirnecrinidae and suggests that only a
small number of plates constituted the
tegmen and that the structure was loosely
sutured. If so, this contrasts strongly
with the multi-plated, prominent, and
rugged tegmen characteristic of the Platy-
crinitidae and militates against that
family as ancestral to the Prokopi-
crinidae.
Family PROKOPICRINIDAE, new family
Diagnosis.—Calyx diminutive, pentagonally
symmetrical, bowl-shaped, confined to patina of 5
RR and three unequal BB, small B in AE inter-
ray; posterior side not differentiated, tegmen
not prominent. Column round, homeomorphic.
Arms and tegminal plating unknown.
Included genus.—Prokopicrinus , new
genus.
Range and _ distribution.—M.—U.
Silurian (Wenlockian-Ludlovian), Ten-
nessee and Oklahoma.
Remarks.—The Prokopicrinidae is
closely related to at least 2 platy-
crinitacean families. It differs from the
Hirneacrinidae in that the latter still
has IRR notching the RR and a dif-
ferentiated CD (posterior) interray. Cri-
noids of the Platycrinitidae are gen-
erally large, have a prominent dome-
shaped tegmen, and possess elliptical
and twisted synarthrially articulated
columns (Lane, 1978; Broadhead and
Strimple, 1977). Such features as strati-
graphic range, reduced tegmen and IRR,
plus the infolded tops of the RR sup-
port direct descent from the Hirne-
acrinidae, rather than either independent
origin from the Hapalocrinidae or deriva-
tion from supposed early platycrinitids.
Though quite small, these crinoids are
adults; no larger calices or isolated
plates have been found despite pro-
tracted search. We do not consider
Prokopicrinus a microcrinoid. Though
the term ‘‘microcrinoid’”’ (sensu lato) can
embrace a fairly wide size range (Arendt,
1970) we prefer to restrict it to those
crinoids having a considerable part of
their potentially preservable ontogenetic
146
development taking place at sizes below
1 mm: such crinoids, we believe, con-
stitute a homogenous group unrelated
to the presently considered forms. For
those macrocrinoids that are unusually
small we propose the term minicrinoid.
Arbitrarily a maximum adult “‘size”’
(A ray-CD interray width at tops of RR)
of 5 mm is a convenient breaking point
while a minimum in excess of | mm (for
the youngest calcified stages) can be
used to delimit the lower end of the
minicrinoid size range. This small size
very probably has functional conse-
quences. Many, if not all, minicrinoids
may have been competing primarily with
microcrinoids and may have been ca-
pable only of tentacular or limited
mucus-net feeding, analogous to the
pentacrinoid larval stage of modern
Articulata.
The simple structure of the calyx
and, especially, the lack of a differ-
entiated anal side makes orientation
difficult. Lacking morphologic criteria
we fall back on phylogeny. The system
adapted here (figs. 1, 12) is based on
the assumption that the genus is a platy-
crinitacean and hence has the small basal
in the AE interray—a defensible but
hard to prove contention.
Genus Prokopicrinus, new genus
Figures 1, 12
Diagnosis, range, and distribution are
the same as those given for the family.
Type species.—Prokopicrinus tuber-
culatus, n. sp., Henryhouse Formation
(Ludlovian).
Derivation of name.—We take con-
siderable pleasure in naming this genus
after Rudolph J. Prokop, Narodni Mu-
seum, Czechoslovakia.
Prokopicrinus tuberculatus, new species
Figures 9-11
Diagnosis.—Calyx depressed, much wider than
high; BB barely visible in side view; plates tumid,
irregularly tuberculate, sutures deeply impressed;
prosopon consists of numerous small tubercles,
irregular in size and arrangement; no basal flange.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
inl
LG
2Po@
oly
2
Fig. 1-2. Plate diagrams: 1, Prokopicrinus; 2, Elicrinus. Infrabasals white, basals
dotted, radials obliquely lined. Presumed A ray uppermost.
Material.—A single specimen, the holotype
(SUI 44341), recovered from weathered material
derived from the upper part of the Henryhouse
Formation, NW 1/4 NW 1/4 SW 1/4 sec. 33, T3 N,
R 6 E, Ahloso quadrangle, Pontotoc County,
Oklahoma.
Description.—Calyx outline rounded to pentag-
_ onal due to slight protrusion of R arm facets
and tumid plate centers; calyx small (see in
Table 1), depressed bowl-shaped. BB 3; 2 equal,
5 sided in plan view (fig. 11), centered in B and
D rays; smaller B (in AE interray) 4 sided in
bottom view; B circlet small, about 4% maximum
calyx diameter, pentagonal, barely visible in side
view (fig. 10). Stem facet protruded slightly,
circular, % width of B circlet; lumen small,
circular. RR 5, equal, making up most of calyx
height, upper edges extending onto oral surface
and covering approximately ¥5 of its area. Arm
facets semicircular, peneplenary, declivate, sur-
rounded by indistinct rim; axial canal not sepa-
rate. Arms and tegmen unknown. Plates thick,
tumid, with moderately impressed sutures; outer
plate surfaces covered irregularly with variously
sized, low rounded tubercles. The tumidity of
the BB gives the impression of an insignificant
basal flange.
Derivation of name.—Suggested by
plate ornament.
Remarks. —P. tuberculatus somewhat
resembles P. barricki in calyx shape
but the details of plate thickness. orna-
ment, and other characters are distinc-
tive. From P. laevis the species can
be differentiated by the less prominent
BB as well as the surficial differences
indicated by the trivial names. The calyx
shape and large arm facets are super-
ficially similar to those of Hirneacrinus.
The species is much larger than the re-
maining 2 (Table 1).
Prokopicrinus laevis, new species
Figures 6—8
Diagnosis.—Prokopicrinus with only slightly
wider than high, bowl-shaped calyx having promi-
nent (in lateral view: fig. 7) BB and smooth
plates without impressed sutures. No B concavity
or flange.
Material.—An isolated calyx lacking the teg-
men; one radial fractured. Provenance same as
preceding species; holotype SUI 44340.
Description.—Calyx outline subcircular except
for barely perceptible protrusion of R arm facets
(figs. 6, 8); diminutive (see Table 1), only slightly
Table 1.— Measurements of Prokopicrinus species (holotypes).
Name A-CD Width Height
_P. tuberculatus 1.83 mm 1.07 mm
P. laevis 1.56 mm 1.10 mm
P barricki 1.43 mm 0.57 mm
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
Calyx
Diameter of width/column
column facet H/Wratio facet width
0.50 mm 0.55 3.66
0.40 mm 0.71 1.42
0.47 mm 0.40 ZO
147
Figs. 3-11. Camera lucida drawings of holotypes of Prokopicrinus species: 3-5, P.
barricki, n.sp. (SUI 44338); 6-8, P. laevis, n.sp. (SUI 44340); 9-11, P. tuberculatus,
n.sp. (SUI 44341). Each set consists of a top, side, and bottom view; all drawings x25.
wider than high. B circlet roughly pentagonal;
B shapes and orientation as in P. tuberculatus;
circlet wide (2 calyx width as viewed from
below), distally protruded from calyx into stem
facet, making up about % of total calyx height
(fig. 7). Stem facet circular, narrow (less than %4
greatest calyx diameter); holotype retains a single
narrow cylindrical columnal with small circular
lumen and crenularium not prominent; 5 equal RR
infolded onto the oral surface in a manner and
degree comparable to P. tuberculatus (fig. 6); arm
facets semielliptical, declivate, much wider than
148
high, approaching full width of RR, notched
proximally by combined axial canal and ambulacral
tract; subdued rim around distal perimeter. Plates
smooth, thick but not tumid, sutures not im-
pressed. No suggestion of basal flange. Arms
and tegmen unknown; latter would roof less than
half of the flattened oral surface.
Derivation of name.—The specific
epithet refers to the unornamented
plates.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
Remarks. —P. laevis is most compara-
ble to P. tuberculatus; specific differ-
ences have been noted under the latter’s
description.
Prokopicrinus barricki, new species
Figures 3—5
_ Diagnosis.—A species of Prokopicrinus charac-
terized by its pentalobate calyx (figs. 4, 6), basal
flange and accompanying narrow basal concavity,
and pitted plate surfaces.
Material.—Three calices (holotype SUI 44338;
unfigured paratypes SUI 44339), from a sample
of Waldron Shale collected by James Barrick,
University of Iowa. The sample was obtained
from an 8 cm thick shale bed immediately
above the Waldron-Laurel contact in the aban-
doned Franklin Limestone Company quarry north
of Clifton, Wayne County, Tennessee (Clifton 714’
quadrangle: Tennessee coordinates 378,000N,
1,412,250E).
Description.—Calyx smail (less than 1.5 mm
wide: see Table 1), pentalobate in plan view, wider
than high; holotype more flat based and de-
pressed than paratypes. Outline of B circlet
rounded, only faintly pentagonal (fig. 5). BB
prominent in side view (fig. 4), distally pro-
duced into basal flange surrounding compara-
tively wide (4% calyx diameter) column facet.
The circular stem facet is impressed into BB; B
concavity has narrow periphery separating stem
facet from basal flange. RR 5, large, much
wider than high, onlapping oral surface less than
in other Prokopicrinus species (fig. 3), produced
into broad lobes strongest near center of upper
edges. Arm facets narrow, almost quadrangular
in shape, not exceeding % greatest R_ width;
orientation nearly horizontal. Facets on lobate
portion of RR, notched by axial canal-ambulacral
tract. All calyx plates with coalescing, irregularly
polygonal, shallow pits; plate sutures not im-
pressed. Proximal columnals (removed in cleaning)
short cylinders with tiny circular lumen; crenu-
larium distinct, simple, narrow. Arms and tegmen
not preserved.
Derivation of name.—The_ species
name honors the collector, James Bar-
rick.
Remarks.—Calyx shape, atypically
wide tegminal region, and narrow arm
facets suggest that P. barricki is more
distantly related to P. laevis and P.
tuberculatus than the 2 latter species
are to each other. Too little is known
about the phylogenetic significance of
specific taxobases in Prokopicrinus to
permit evaluation of interrelationships
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
at the species level. The peculiar surface
features, reminiscent of the outside sur-
face of hammered aluminum kitchen
ware, are rare among crinoids; the un-
related disparid inadunate Apodasmo-
crinus punctatus (Brower and Veinus,
1974) is the closest parallel.
Paleoecology
Boucot (1975: 206) interprets the
Henryhouse and Waldron brachiopods
as quiet water communities. Supporting
this assessment are the fine-grained
matrix and the abundance of unusually
small brachiopod taxa. The suite of
genera found in the Waldron sample best
fits the Dicoelosia-Skenidioides Com-
munity of Benthic Assemblage 4 (Boucot,
op. cit.: fig. 4 and p. 247) and may
represent a deeper environment of dep-
osition than does the typical Waldron.
All brachiopods recovered are small,
Sphaerirhynchus is absent and Atrypa
is rare, while Dicoelosia, Nucleospira,
Coelospira, and Skenidioides are un-
usually abundant. Dalejina, Reserella,
Isorthis, and MHowellela are equally
represented in both areas. Pelecypods
are extremely rare, and few corals are
present. Ostracods and bryozoa are
most conspicuous in abundance after
brachiopods and echinoderms, but
sponges are also present. Conodonts
are exceedingly rare. Echinoderm genera
include common Stephanocrinus, Le-
canocrinus pusillus, *‘Deltacrinus’’ stig-
matus, and Pisocrinus s. 1. The last
has not previously been found in the
Waldron; other such genera (besides
Prokopicrinus) include Zophocrinus, an
undescribed pygmaeocrinid, and Thala-
mocrinus. Many forms common in the
typical Waldron are rare or absent here
(e.g., Eucalyptocrinites, Macrostylo-
crinus, and Lyriocrinus) while others
which are normally uncommon become
relatively abundant (calceocrinids, mi-
crocrinoids). Other echinoderms, includ-
ing Decaschisma (Blastoidea) and cyclo-
cystoids, are present in about equal
numbers in both.
The Henryhouse Prokopicrinus-yield-
149
ing sample is quite similar. The flexible
crinoid Lecanocrinus and some inadu-
nates (Pisocrinus , Gissocrinus) are com-
mon, while large camerates are rela-
tively rare. As in the Waldron sample,
microcrinoids’ and calceocrinids are
abundant. Zophocrinus is among the
characteristic genera, while some forms
not previously reported from the Henry-
house (undescribed pisocrinid, Hexa-
crinites sp.) are also present. The
brachiopod fauna of the Henryhouse
wuwue &
constitutes the only cited example of
the Dicoelosia—Orthostrophella Com-
munity (Benthic Assemblage 3) of Bou-
cot (1975: 249) (=Henryhouse Com-
munity of Boucot, 1970). Those in our
sample show a generic composition and
relative abundances much like those
in the Waldron sample, from which
we have not yet recovered Ortho-
strophella.
The value of the echinoderm taxa as
environmental indicators is not well
o° Oo
@owwewe
(2
“eo eZ oo” w
| >
oe
Figs. 12-14. Plate diagrams showing presumed evolution of the Prokopicrinidae:
12, Hagnocrinus (Hirneacrinidae); first interradials (including larger primanal) still
notching radials; 13, hypothetical intermediate form with primanal only still in cup;
14, Prokopicrinus. Rays lettered according to Carpenter system; basals white, radials
black, lateral first interradials stippled; primanal scored obliquely.
150
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
established. Pisocrinus s.1. occurs in a
variety of habitats (Ausich, 1977) but is
perhaps most characteristic of moder-
ately deep and quiet water and soft
bottoms: Ausich (1977: 684) interprets
it as a low-energy rheophile. Gisso-
crinus was found by Lowenstam (1957)
to be restricted to less turbulent en-
vironments in the northeastern Illinois
Silurian. The genus is abundant in the
Laurel, the echinoderm-bearing part of
which may have been deposited in
moderately deep water with relatively
weak currents and a slow sedimenta-
tion rate (Frest, 1975). It is absent from
the Racine reefs but flourishes in the
non-reefal Brownsport (Springer, 1926).
Certainly its bizarre arm morphology
(Springer, 1926: 135-137) is unlikely
to be competitive in turbulent environ-
ments. Similar conclusions can be drawn
from the small inadunates. Breimer and
Macurda (1972: 300) suggest that piso-
crinids and microcrinoids formed a rheo-
phobic understory in crinoid communi-
ties with abundant large rheophiles.
Whether these crinoids are termed low-
energy rheophiles or rheophobes is pri-
marily semantic; a relatively quiet en-
vironment is suggested.
A small sized brachiopod assemblage
suggests a soft-bottom, quiet water
habitat (Boucot, 1975). Brower (1975)
and Watkins and Hurst (1977) interpret
Silurian small-sized crinoid assemblages
similarly. The latter authors emphasize
the soft bottom aspect as the controlling
factor (Watkins and Hurst, 1977: 213-
216). This is certainly not always the
case, as some large camerates like the
Silurian-Devonian Eucalyptocrinites
thrived equally well on soft or hard
substrates (Halleck, 1973 and personal
observation), while, as acknowledged
by Watkins and Hurst (1977: 216),
such diverse assemblages as that at
Crawfordsville (Lane, 1973) belie the pre-
sumed connection between substrate and
crinoid size and diversity in the later
Paleozoic. Combined with some other
factors (mentioned above) the sugges-
tion may have merit.
In the present examples other lines
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
of evidence can be cited aside from
size and substrate. Some of the brachio-
pods and most echinoderms are dis-
articulated. No crowns have been re-
covered and there is little indication
that either brachiopods or echinoderms
are in life position. This is consistent
with a low or moderate rate of sedi-
mentation; transport is here not plausibly
a factor of importance. Overall, the
evidence suggests a relatively quiet
water, soft bottom environment, with
sediment accumulation taking place at a
moderate depth and at a comparatively
slow rate. The similarities between the
two faunas (abundant Pisocrinus , micro-
crinoids, and calceocrinids, similar ge-
neric composition, with common inadu-
nates and flexibles and scarce camerates;
small individuals) may indicate the exist-
ence of a discrete assemblage that is a
parallel to the brachiopod-based Benthic
Assemblage 4 of Boucot; this possi-
bility requires further investigation,
however.
Affinities
A crinoid with a plate configuration
like that of Prokopicrinus could be either
an inadunate or camerate. Our choice
of the latter, as discussed above, is
based in part on the morphology of the
basal circlet and even more on the
overall resemblance of the genus to some
definite camerates (platycrinitaceans,
noteably the hirneacrinids) and on the
reconstruction of phylogenetic trends
within the Platycrinitacea. As these have
been the subject of 2 recent papers
(Brower, 1973; Frest and Strimple, 1977)
as well as having been outlined above,
the arguments will not be recapitulated
here. A tentative phylogeny of the rele-
vant families is presented as Figure 15.
The addition of the Hirneacrinidae
and Prokopicrinidae to the picture serves
mainly to emphasize the distinctness of
the Platycrinitacea from the Patellio-
crinacea. The former, including some
of the most morphologically specialized
(evolutionarily advanced?) camerates,
shows a conspicuous tendency toward
151
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Fig. 15. Possible phylogeny of the patelliocrinacean and platycrinitacean families.
Superfamily Patelliocrinacea dotted; Platycrinitacea crosshatched.
acquisition of inadunate-like cup [here
better termed calyx (Ubaghs, 1978)]
features. This divergence from main
camerate lines (i.e., crinoids with a
many-plated dorsal cup including fixed
brachials and numerous plates in inter-
radial position) was evidently only par-
tially successful. The early platycrini-
tacean families (Hapalocrinidae, Hirnea-
crinidae, and Prokopicrinidae) are, with
few exceptions, not particularly diverse
or numerous, but the Platycrinitidae are
sometimes spectacularly abundant in
upper Paleozoic rocks and include many
of the last surviving camerates. The
superfamily combines the advantages of
the inadunate cup (smaller and mechani-
cally more rugged than the typical came-
rate calyx) with the advanced arm fea-
tures characteristic of the camerates
from their earliest appearance. Once
the transition from uniserial or cuneate
pinnulate arms to totally biserial was
made (in Silurian hapalocrinids) there
is little further arm evolution in the
superfamily, but the calyx becomes
progressively more inadunate-like.
The earliest Patelliocrinacea (e.g.,
Eopatelliocrinus) resemble other con-
temporary camerates, but trends toward
152
reduction in number of calyx plates
and simplification to a patina were ini-
tiated very early in the superfamily’s
history. They are already evident, for
example, in the Upper Ordovician
Macrostylocrinus pristinus (Brower,
1973). Within the Patelliocrinacea these
tendencies are accentuated in the short-
lived Marsupiocrinidae and Stelidiocrini-
dae; both of these groups, however,
retain some fixed IRR and arm brachials,
and the marsupiocrinid tegmen is many-
plated and without distinguishable orals.
Exacerbation of the trend toward expul-
sion of the IRR led to the develop-
ment of the Hapalocrinidae, members of
which still have one IR series and
proximally fixed arms. The hapalocrinid
tegmen, while simple in comparison to
that of patelliocrinids, is many-plated
and includes both ambulacrals and inter-
ambulacrals, as well as distinct orals
and the so-called axillary ambulacrals
(Breimer, 1962) in some genera. Con-
tinued evolution along the same lines
resulted in 2 separate lineages. The
hirneacrinid lineage, which includes the
Prokopicrinidae, rapidly acquired totally
free arms and eventually completely
eliminated interradially situated plates
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
from the calyx. The resultant calyx is
fully pentagonally symmetrical and there
is no differentiation of the posterior
interray. Body volume is reduced, and
the tegmen dwindles in size.
In the platycrinitid line the tegmen
continues to serve a major role. In
many Permian and Carboniferous species
it is dome-like and rigid, apparently
housing part of the body mass as well
as the organ systems closely clustered
about the mouth. Most platycrinitids
were robust animals obviously capable
of full mucus-net feeding. Some genera
and species ultimately considerably sim-
plified the tegmen (e.g., Broadhead &
Strimple’s [1977] species) but others
either retained unchanged or secondarily
acquired a hapalocrinid-like tegmen
(Breimer, 1962). In contrast to the short-
lived specialized Silurian families the
Platycrinitidae probably represent the
main line of evolution in the super-
family and are very likely direct lineal
descendants of early Devonian hapalo-
crinids. Reduction in calyx size, the
noted tegmen modifications, and expul-
sion or elimination of fixed IRR in the
Marsupiocrinidae could have produced a
form like Prokopicrinus , but no connect-
ing links are known and the hirneacrinid
antecendents of the genus can be derived
more readily from the Hapalocrinidae.
Even fewer steps could produce an iden-
tical form from platycrinitid predecessors
but again no intermediates are presently
available: additionally, the oldest un-
doubted platycrinitids are Devonian in
age (Oenochoacrinus). Derivation of the
prokopicrinids from the hirneacrinids
would require only continued upward
migration of the first IRR, already barely
participating in the cup in Hagnocrinus.
An intermediate step, as yet undis-
covered, with only the CD IR (primanal)
notching the calyx, is probable (see
Figures 12-14).
Similar-appearing forms have been
reported among the Inadunata. Some
microcrinoids (e.g., Amphipsalidocrinus)
have comparable plate arrangements,
and an Amphipsalidocrinus-like form
(undescribed) does occur in the Waldron.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
However, the microcrinoids, aside from
their smaller size, typically have orals
that are very prominent and essentially
a part of the calyx. Radials are seldom
as well developed, many genera are
partly or wholly abrachiate, and most
have an anal opening in the side of the
cup; ontogenies and detailed descriptions
of the relevant taxa are in Arendt’s (1970)
comprehensive monograph. The oldest
documented true microcrinoid occur-
rences are Devonian, but the group is
now known to range down into the
Ordovician (C. R. C. Paul, personal
communication, 1977) and we have
Silurian forms from several horizons.
Small Devonian crinoids originally re-
ported as juveniles of the camerate
(hapalocrinid) Cyttarocrinus eriensis
(Hall) by Koenig (1965) have a plate
arrangement identical to that of Pro-
kopicrinus. However, the type B (of
Ausich, 1977) pisocrinid-like arm facets
and fixed orals of these crinoids suggest
that they are disparid inadunates related
to Haplocrinites; this interpretation will
be documented in a later paper. These
specialized features are not present in
the Prokopicrinidae, thus removing them
from consideration as possible ante-
cedents to the Silurian group.
An even more remarkable example of
parallel evolution is afforded by the
cladid Elicrinus (Prokop, 1973) from the
Lower Devonian of Bohemia. Elicrinus
is perfectly pentagonal, has no anal
plates, and has a restricted tegmen and
prokopicrinid-like radial arm facets. If
the calyx is viewed from above the
resemblance to Prokopicrinus is perfect
(Prokop, 1973: plate 1, fig. 3). However,
Elicrinus is dicyclic and cone-shaped
(compare figs. 1 and 2); accepting the
fundamental nature of the monocyclic-
dicyclic ‘‘schism’’ (Warn, 1975) the two
cannot be closely related. The prob-
lematical nature of any effort to ac-
comodate such superficially simple forms
in the present classificatory system is
well demonstrated by Elicrinus: no
evolutionary intermediates are known
and the same crinoid could have equally
well derived from half a dozen cladid
153
families. Prokop wisely chose to leave
the genus unassigned as to family (1973:
221). Our own procedure here is perhaps
rash, but we believe that our case is solid
enough to justify more complete treat-
ment than was possible with the dicyclic
form.
Yet another possibility is that the
known Prokopicrinus species are young
representatives of an as yet largely un-
discovered lineage of true inadunates.
Any number of disparid families with
documented records extending into the
Ordovician or Silurian could have given
rise to a prokopicrinid-like form (e.g.,
the Homocrinidae, Synbathocrinidae, or
Ramacrinidae). Again, the problem of
missing intermediates prevents resolu-
tion of the family’s phylogenetic rela-
tionships. Whatever the eventual dis-
position of the group on available evi-
dence, differentiation as a distinct family-
level taxon seems inevitable regardless
of which alternative progenitor is se-
lected.
Acknowledgements
We thank Thomas W. Broadhead and
Brian J. Witzke (University of Iowa)
for helpful criticism of an earlier draft.
References Cited
Arendt, Y. A. 1970. Morskie lilii hipokrinidy,
Akad. Nauk USSR, Trudy Paleontologicheskogo
Inst., 128, 220 p., illus.
Ausich, W. I. 1977. The functional morphology and
evolution of Pisocrinus (Crinoidea: Silurian).
Jour. Pal., 51(4): 672-686, illus.
Boucot, A. J. 1970. Practical taxonomy, zoo-
geography, paleoecology, paleogeography and
stratigraphy for Silurian and Devonian brachio-
pods. Proc. N. American Pal. Convention I,
F: 566-611.
1975. Evolution and Extinction Rate
Controls. Elsevier, Amsterdam, 427 p., illus.
Breimer, A. 1962. A monograph on Spanish
Palaeozoic Crinoidea. Leidse Geol. Medede-
lingen, Overdruk 27, 190 p.
, and D. B. Macurda, Jr. 1972. The phylogeny
154
of the fissiculate blastoids. Koninkl. Nederl.
Akademie van Wetenschappen Amsterdam,
Verh., Afdel. Naturkunde, erste reeks, 26(3),
390 p., illus.
Broadhead, T. W., and H. L. Strimple. 1977.
Permian platycrinitid crinoids from Arctic North
America. Canadian Jour. Earth Sci., 14(5):
1166-1175, illus.
Brower, J. C. 1973. Crinoids from the Girardeau
Limestone (Ordovician). Palaeontographica
Americana 7: 263—499. hee
. 1975. Silurian crinoids from the Pentland
Hills, Scotland. Palaeontology, 18: 631-656,
illus.
, and J. Veinus. 1974. Middle Ordovician
crinoids from southwestern Virginia and eastern
Tennessee. Bull. Amer. Pal., 66(283), 125 p.,
illus.
Frest, T. J. 1975. Caryocrinitidae (Echinodermata:
Rhombifera) of the Laurel Limestone of south-
eastern Indiana. Fieldiana: Geol., 30: 81-106.
, and H. L. Strimple. 1977. Hirneacrinidae
(new), simple Silurian camerate crinoids from the
North American Continental Interior. Jour.
Pal., 51: 1181-1200.
Hall, J. 1878. The fauna of the Niagara Group
in Central Indiana. N. Y. State Mus., Ann.
Rept., 28: 99-204.
Halleck, M. S. 1973. Crinoids, hardgrounds, and
community succession: The Silurian Laurel-
Waldron contact in southern Indiana. Lethaia,
6: 239-252, illus.
Koenig, J. W. 1965. Ontogeny of two Devonian
crinoids. Jour. Pal., 39(3): 398-413.
Lane, N. G. 1978. Family Platycrinitidae. Jn
Treatise on invertebrate paleontology, part T
(Echinodermata 2). Lawrence, Kansas (in press).
Lowenstam, H. A. 1957. Niagaran reefs of the Great
Lakes area. Jn H. S. Ladd (ed.), Treatise on
marine ecology and paleoecology. Geol. Soc.
Amer., Mem., 67(2): 215-248.
Prokop, R. J. 1973. Elicrinus.n. gen. from the
Lower Devonian of Bohemia (Crinoidea). Vest-
nik Ustredniko ustavu geologickeho, 48: 221-
224, illus.
Springer, F. 1926. American Silurian crinoids.
Smithsonian Inst. Pub. 2871, 239 p., illus.
Strimple, H. L. 1963. Crinoids of the Hunton
Group (Devonian-Silurian) of Oklahoma. Okla-
homa Geol. sur. Bull. 100, 169 p., illus.
Ubaghs, G. 1978. Camerata. In Treatise on In-
vertebrate paleontology, part T (Echinodermata
2). Lawrence, Kansas (in press).
Warn, J. M. 1975. Monocyclism vs. dicyclism:
a primary schism in crinoid phylogeny? Bull.
Amer. Pal., 67(287): 423-441.
Watkins, R., and J. M. Hurst. 1977. Community
relations of Silurian crinoids at Dudley, England.
Paleobiology, 3(2): 207-217.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
Myliasis in the Eastern Box Turtle Caused
by Phaenicia coeruleiviridis (Diptera: Calliphoridae)!
Jay Abercrombie’
U. S. Army Environmental Hygiene Agency, Regional Division—North,
Fort George G. Meade, Maryland 20755
ABSTRACT
Larvae of Phaenicia coeruleiviridis (Macquart) (Diptera:
Calliphoridae) were
discovered causing facultative wound myiasis in the eastern box turtle, Terrapene
carolina carolina (L.) (Testudines: Emydidae), in Maryland. Eight larvae were recovered
from a puncture wound in the turtle’s body wall near the head. Adult flies emerged
after a pupal period of 7 days. The turtle subsequently died.
Larvae of certain flies commonly infest
wounds or traumatized tissues of man
and animals. Often the larvae confine
their feeding or scavenging to necrotic
tissues at the site of a wound or some
other lesion on the skin. Occasionally
these secondary larval invaders continue
to burrow beneath the dead flesh into
healthy tissues or organs, resulting in
serious injury or even death to the host.
Such an infestation generally is termed
facultative myiasis.
This paper reports a case of facultative
wound myiasis caused by larvae of
Phaenicia coeruleiviridis (Macquart) (Dip-
tera: Calliphoridae) in the eastern box
turtle, Terrapene carolina carolina (L.)
(Testudines: Emydidae). Eight mature,
third-instar larvae of P. coeruleiviridis
were obtained from a suppurating wound
in a turtle collected 2 September 1976 in
Millersville, Maryland.
The infected turtle was about 10 cm
long and 7.5 cm wide. It appeared lethargic
and weak; the front hinge of the plastron
could be pried open with an index finger.
The turtle had suffered a puncture wound
1 The opinions or assertions contained herein are
‘the private views of the author and are not to be
construed as reflecting the views of the Department
of the Army or the Department of Defense.
2 Present address: Chemical Systems Laboratory,
Ecology Branch, Aberdeen Proving Ground, Mary-
land 21010.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
in the body wall dorsolaterad to the head
and ventrad to the carapace. The opening
formed by the wound was about 6 mm in
diameter and over 20 mm deep, extending
well into the body cavity. The wound was
festered and was oozing a malodorous
brown fluid. Several dipterous larvae
were observed crawling in the wound
cavity and making their way to the
opening where they extruded their pos-
terior spiracles in order to obtain oxygen.
The turtle was transported to the lab-
oratory and placed in a cage for ob-
servation.
Four larvae were plucked from the
opening with forceps as they surfaced
for air. These specimens were killed
and preserved. On 3 September, two ad-
ditional larvae were removed and placed
in sand at room temperature so that they
would pupate. A seventh larva was
found crawling across the floor of the
cage on 4 September; it was collected
and placed in a separate jar of sand. On
5 September, an eighth and final larva
was pulled from the wound and set up
in another jar of sand. While probing with
forceps, small pieces of loose, fiat,
calcified tissue also were removed from
the turtle’s body cavity.
None of the four larvae in sand had
pupated by 8 September so they were
placed in an environmental chamber at
13°C. The larvae pupated on 10 Septem-
155
ber. The pupae were set up in separate,
stoppered vials and retained at room
temperature. Adults emerged from two of
the puparia on 17 September after a pupal
period of 7 days; the other pupae failed
to produce adults.
The flies were identified by R. J. Gagné,
Systematic Entomology Laboratory,
U. S. Department of Agriculture, Wash-
ington, D. C., as P. coeruleiviridis. This
species is common in woods and fields
where it has been collected upon human
excrement and decaying meats (Hall,
1948). Phaenicia coeruleiviridis also has
been reared from nests of starlings
(McAtee, 1929), and females were ob-
served ovipositing upon the fur of a thin
and emaciated kitten by Davis (1928).
The animal was weak and ill but sup-
posedly was not wounded.
The present paper is the first apparent
report of larvae of P. coeruleiviridis
causing myiasis in a vertebrate and the
first recorded association between calli-
phorids and turtles. Cistudinomyia cis-
tudinis (Aldrich), a sarcophagid fly, has
been bred from sores in box turtles
(Aldrich, 1916; Knipling, 1937), but this
Species is apparently an obligate parasite,
156
not a facultative producer of myiasis as
P. coeruleiviridis .
The turtle’s wound remained fetid and
suppurative even after the last calliphorid
larva had been removed. The turtle
continued to be very weak and inactive.
It never drank or ate while in the labora-
tory, and seldom moved about the cage.
It died on 30 September, 28 days after
capture, probably as a result of the
fly infestation.
All specimens of P. coeruleiviridis
were deposited in the U. S. National
Museum.
References Cited
Aldrich, J. M. 1916. Sarcophaga and allies in
North America. [Vol. 1], 301 pp., 16 pls.
Entomol. Soc. Amer., Thomas Say Foundation,
Lafayette.
Davis, W. T. 1928. Lucilia flies anticipating death.
Bull. Brook. Entomol. Soc. 23: 118.
Hall, D. G. 1948. The blowflies of North America.
[Vol. 4], 477 pp., 5 pls. Entomol. Soc. Amer.,
Thomas Say Foundation, Baltimore.
Knipling, E. F. 1937. The biology of Sarcophaga
cistudinis Aldrich (Diptera), a species of Sarco-
phagidae parasitic on turtles and tortoises. Proc.
Entomol. Soc. Wash. 39: 91-101.
McAtee, W. L. 1929. Further notes on insect
inhabitants of bird houses. Proc. Entomol. Soc.
Wash. 31: 105-111.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
Parasitism of Trirhabda virgata LeConte
(Coleoptera: Chrysomelidae)
by a species of Aplomyiopsis Villenueve
(Diptera: Tachinidae)
Owen DeVer Sholes
Section of Ecology and Systematics, Cornell University,
Ithaca, New York 14853
ABSTRACT
Of 69 larvae of Trirhabda virgata reared in the laboratory, 2 yielded tachinids
of the genus Aplomyiopsis.
As part of a project concerning the
arthropod fauna of Solidago Linnaeus
in old fields near Ithaca, New York,
phytophagous insect larvae found on or
near goldenrods were reared in the lab
for identification, and to see whether the
larvae were targets of parasitoids fre-
quenting goldenrod inflorescences later
in the season. One such culture consisted
of larvae of the chrysomelid Trirhabda
virgata LeConte, abundant on Solidago
altissima Linnaeus, and occasionally on
other Solidago species.
On May 30, 1977, I collected numerous
larvae, mostly last instar, and placed
them in a glass quart jar with fine-mesh
Dacron organdy stretched tightly over
the mouth. Room temperature varied be-
tween 20° and 24°C. Fresh S. altissima
leaves were added and old leaves were
removed at least every other day. By
June 13, 1977, the larvae had stopped
feeding and most had curled up on the
bottom of the jar. Two larvae did not
curl, and each appeared to have a fly
puparium inside the larval skin. On June
8, 11, and 13, 1977, all 69 larvae in the
culture were transferred to the surface
of a dampened peat moss-vermiculite
mixture, partitioned in four cylindrical
glass dishes (2.7 cm high, 5.4 cm inside
diameter) with glass covers. One larva
appeared to be diseased, being almost
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
entirely covered with a white, velvety,
probably fungal coating.
The 2 larvae containing puparia each
yielded a tachinid of the genus Aplomyi-
opsis Villenueve (they may belong to an
undescribed species (C. W. Sabrosky,
personal communication); both specimens
are in the U. S. National Museum). One
emerged on June 11, 1977, and the other
on June 16, 1977. Both flies emerged
from the posterior end of the old larval
skin. The remaining ‘‘undiseased’”’ larvae
eclosed between June 18 and July 1, 1977.
Thus, of the 69 larvae, 1.4% were ‘‘dis-
eased’’, 2.9% were parasitized by
Aplomyiopsis sp., and 95.7% survived to
eclosion.
According to Clausen (1940, Entomoph-
agous Insects, McGraw Hill, New York,
p. 430) and Sabrosky and Arnaud in
Stone et al. (1965, A Catalog of the
Diptera of America North of Mexico,
U2-S) Dept. Agr., Agr..Res. Serv.,
Agricultural Handbook No. 276), the
species of Aplomyiopsis attack larvae
of Chrysomelidae and phytophagous
Coccinellidae. This report of Aplomyi-
opsis sp. attacking the larvae of T.
virgata is further documentation of the
parasitism of chrysomelid larvae by the
genus Aplomyiopsis and is the first
record of a tachinid parasite attacking
the genus Trirhabda.
Parasitism of 2.9% of the T. virgata
larvae seems to be quite low for an
abundant, externally-feeding herbivore.
By contrast, 16-90% of Mexican bean
beetle larvae, Epilachna varivestis Mul-
sant, were parasitized by Aplomyiopsis
epilachnae (Aldrich) in Mexico and the
United States (Landis and Howard,
1940, Paradexodes epilachnae , atachinid
parasite of the Mexican bean beetle,
U: S.. Dept, Agr. Tech--Bul. Noy 722:
1-—31.). Of course, the 7. virgata larvae
in this culture were not exposed for
158
their entire larval lives, nor during their
pupal period, which may also be vulner-
able (Clausen, 1940 ibid.). However, now
that Aplomyiopsis sp. has been identified
as a parasite of T. virgata, its impact
on T. virgata can be more precisely
assessed in future work.
Acknowledgments
I want to thank C. W. Sabrosky for identifying
the 2 Aplomyiopsis, and E. R. Hoebeke for
identifying several T. virgata adults. E. R.
Hoebeke, C. R. Sholes, and R. H. Whittaker
provided many helpful comments.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
ACADEMY AFFAIRS
NEW FELLOWS
Henry Parsons, Executive Director,
Institute for Behavioral Res., Inc., Silver
Spring, Md., in recognition of his con-
tributions to human factors/engineering
psychology and to behavioral psychology
(operant conditioning), in particular his
work in man-machine systems and their
training and experimental evaluation.
Sponsors: John O’ Hare, Sherman Ross,
J. E. Uhlaner.
Tom van der Zwet, Research Plant
Pathologist, USDA, in recognition of his
research in fire blight of apple and
pear, and in particular his contributions
to breeding for blight resistance in pear.
Sponsors: R. R. Colwell, Richard H.
Foote.
INFORMATION ON SOCIETIES RECENTLY AFFILIATED
Potomac Division, American
Phytopathological Society
Objectives: To bring together plant
pathologists to discuss research in plant
pathology and other problems of general
interest and to stimulate understanding
with other sciences concerned with the
general problem of crop improvement.
Members: Active members must be
members of the American Phytopatho-
logical Society. Persons who are not
members of the APS but are interested
in plant pathology are eligible for
Associate Membership. Retired plant
pathologists are considered honorary
members. There are 238 members (from
DW @. Md... Va, Del.,, N..J., N. C.,-&
Yonkers, N. Y.) in the Division.
Meetings: One principal meeting is held
each year with formal programs of
scientific interest. At the 1976 meeting
held at the Univ. of Delaware on
March 17-19, a total of 50 papers were
presented before various groups.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
Metropolitan Washington Chapter of the
Society for General Systems Research
Objectives: (1) To investigate the iso-
morphy of concepts, laws and models
from various fields, and to help in useful
transfers from one field to another: (2)
to encourage development of adequate
theoretical models in fields which lack
them: (3) to minimize the duplication of
theoretical effort in different fields: and
(4) to promote the unity of sciences
through improving communication
among specialists.
Members: The membership is composed
of professional, scientific, and academic
people whose interests are broader than
a particular discipline and who are pur-
suing the systems point of view for deal-
ing with complex problems. There are
now 100 members in the Washington
Chapter.
Meetings: The chapter sponsors an
annual meeting at which papers are
presented and research areas discussed.
159
The 1975 meeting held Sept. 19-20
was concerned with ‘‘Systems Science
and the Future of Health.’’ The topic of
the 1976 meeting is to be ‘‘Complexity:
A Challenge to the Adaptive Capacity of
American Society.”’
Potomac Chapter, Human Factors Society
Objectives: To (1) provide a professional
forum for the exchange of multi-dis-
ciplinary ideas and information about
man and his environment: (2) encourage
a social relationship where members can
meet and communicate freely with others
who have a wide variety of viewpoints
and backgrounds: (3) establish a point of
contact for persons and organizations in
the Potomac Chapter area who are in-
terested in or have a need for human
factors research and technology. == =
Members: Must be members of the —
National Society. Individuals not qualify- —
ing for the election to the grade of
member who are interested or active in
the field may become associate members.
Such members may not vote or become
officers. The chapter consists of 181
members.
Meetings: Not less than one regular
meeting is held each year. Special meet-
ings may be called on request of 15
members. The principal 1975 meeting
was a one day symposium on ‘‘Advance
Technologies in Systems Operation and
Control.’’ In 1976 there was a one-day
symposium on ‘Training: Technology to
Policy.”’
SCIENTISTS IN THE NEWS
NATIONAL COUNCIL OF
ASSOCIATIONS FOR POLICY
SCIENCES
John G. Honig was elected to be president
of NCAPS at arecent election. Dr. Honig
is associated with the Office of the Chief
of Research, Development and Acquisi-
tion, Department of the Army, and has
received wide recognition in the profes-
sional community. He is a founding
member and past president of the
Washington Operations Research Society
and a Past President of the Military
Operations Research Society. He is
also a co-recipient of its David A.
Rist prize for the best paper given at a
symposium. Dr. Honig is also past chair-
man of the Military Applications Section
of the Operations Research Society of
America, a past treasurer and member of
the board of directors of the Washington
Academy of Sciences. He is a member of
the Governor’s (Maryland) Science Ad-
visory Council and a Fellow of the
American Association for the Advance-
ment of Science. In recognition for his
many achievements he was elected to
the Cosmos Club.
160
AMERICAN SOCIETY OF
CIVIL ENGINEERS
Eugene W. Weber, Washington, D. C.,
consulting engineer, today received the
Julian Hinds Award from the American
Society of Civil Engineers. The award
was presented at the Society’s 125th
Annual Convention which is being held
here this week.
The Award was endowed in 1974 in
recognition of the outstanding profes-
sional contributions of Julian Hinds,
Honorary Member of ASCE. The Award
is made annually to the author of that
paper which is judged to be the most
meritorious contribution to the field of
water resources development.
Mr. Weber receives this award for
‘‘distinguished service in planning water
resources for the U. S. Corps of
Engineers and the International Joint
Commission; in particular for leader-
ship in reorienting planning concepts in
the Corps toward socio-environmental
goals, public participation, and greater
consideration of alternatives.’’
From 1931 to 1965 he was in the career
civil service of the Corps of Engineers,
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
Department of the Army engaged in
water resource development, planning
and policy. His responsibilities’ cul-
minated in assignments with the Corps of
Engineers in Washington, D. C. ‘as
Special Assistant to the Director of Civil
Works, Chief of the Civil Works Planning
Division, and Deputy Director of Civil
Works for Policy. For these efforts, Mr.
Weber received the Rockefeller Public
Service Award in 1963, and the Defense
Department Distinguished Civilian Serv-
ice Award in 1963, and the Defense
Department Distinguished Civilian Serv-
ice Award in 1963. In 1963 he also
received the Army’s Exceptional Civilian
Service Decoration, the highest award
that can be given by the Army to a
civilian employee. He retired from
Federal civil service in 1965.
During World War II, Mr. Weber
entered into active Army service from
his reserve status as a Captain, served
in Washington, London, Normandy, and
Paris and returned to civilian status as a
reserve Colonel.
In 1948, Mr. Weber was appointed by
President Truman to serve as a Com-
missioner on the United States Section of
the International Joint Commission,
United States and Canada. He continued
in this position after his civil service
retirement in 1965 and until President
Nixon accepted his resignation in July
1973. During that period of nearly 25
years under five Presidents, he was
heavily involved in the problems of
the Columbia River, Passamaquoddy
Tidal Power, the St. Lawrence Project,
and the air and water pollution studies
in the Great Lakes which are currently a
major concern of the Commission.
Since 1965, Mr. Weber has served as a
consultant to the Organization for Eco-
nomic Cooperation and Development
(OECD) and for several Federal, state
and private agencies.
OBITUARY
William R. Osgood
Dr. William Ruprecht Osgood, 82 died
Sunday, September 25, 1977, at Holy
Cross Hospital in Silver Spring, Md.,
after a brief illness. William Osgood, the
oldest of three children of Professor
William Fogg Osgood and Theresa
Ruprecht Osgood, was born in Cam-
bridge, Mass., on April 17, 1895. He was
a great, great grandson of Dr. George
Osgood and Elizabeth Otis, a daughter of
General Joseph Otis, brother of the
patriot James Otis.
Osgood attended Cambridge High and
Latin School before entering Harvard
College from which he graduated in 1917.
He continued his education at the Massa-
chusetts Institute of Technology and at
the University of Illinois, where he was
awarded an S.M. in engineering in 1924
and a Ph.D. in 1933.
Osgood’s professional career in en-
gineering extended over fifty years and
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
was divided between teaching and
research. His first position was as an
aeronautical engineer in the Research
Department at McCook Field in Dayton,
Ohio, during World War I. After receiv-
ing an S.B. in Mechanical Engineering
from MIT in 1919, he became an assistant
in mechanical engineering there and later
an instructor in theoretical and applied
mechanics in the College of Engineering
of the University of Illinois. From
1926-29 he was assistant professor of
structural engineering at Cornell Univer-
sity. In 1929 he joined the staff of the
National Bureau of Standards as a
Materials Engineer where he worked on
research problems in the Engineering
Mechanics Section and conducted theo-
retical and experimental investigations in
engineering materials and _ structures.
From 1946-50 he worked on structural
research problems of interest to the
Navy’s Bureau of Ships at the David
Taylor Model Basin. At the Model Basin
161
he planned and supervised research pro-
grams on structural problems involving
elasticity and plasticity of materials used
in the design of ships.
In 1950 Dr. Osgood returned to the
academic world as Professor and Chair-
man of the Department of Mechanics at
the Illinois Institute of Technology,
where he administered the department
and taught courses in mechanics. From
1955 to 1960 he was Head of the Depart-
ment of Mechanics at Rensselaer Poly-
technic Institute in Troy, New York.
Having reached the age of 65, he retired
in June 1960 as Professor Emeritus of
Mechanics. His teaching and writing
career was not yet over, however, and
for the next nine years he was a lecturer
and professor of civil engineering at the
Catholic University of America in Wash-
ington where he contributed to the
scientific and educational development of
the engineering school and helped to
build it into an important center in the
field of mechanics. During his career
Osgood published nearly 70 technical
papers and was editor for the National
Research Council of Residual Stresses
in Metals and Metal Construction.
162
Osgood was a Member of the Society
for Experimental Stress Analysis and the
Society of Sigma Xi and a Fellow of the
American Society of Mechanical En-
gineers, the American Society of Civil
Engineers, the Washington Academy of
Sciences and the American Association
for the Advancement of Science. He also
belonged to the Philosophical Society of
Washington, the Harvard Club of Wash-
ington and the Cosmos Club. In 1970 he
was awarded the Technical Achievement
Certificate of the Washington, D.C.
Section of the American Society of
Mechanical Engineers. He was active in
several committees of various profes-
sional societies and served on two
advisory committees of the National
Research Council.
Osgood married the late Albertine
Walther in 1922. They were divorced in
1939; there were no children. He is sur-
vived by a sister-in-law, Margaret
Osgood, of Norton, Mass., and a
nephew, Theodore Osgood, of Chevy
Chase. William Osgood joined the Re-
ligious Society of Friends in 1923 and
since that time maintained membership
in the Swarthmore Monthly Meeting.
J. WASH. ACAD. SCI., VOL. 67, NO. 4, 1977
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