TRANSACTIONS
OF THE
WISCONSIN ACADEMY
OF
SCIENCES, ARTS AND LETTERS
VOL. XXXVI
NATURAE SPECIES RATIOQUE
MADISON, WISCONSIN
1944
TRANSACTIONS
OF THE
WISCONSIN ACADEMY
OF
SCIENCES, ARTS AND LETTERS
VOL. XXXVI
NATURAE SPEC5ES RATIQQUE
MADISON, WISCONSIN
1944
OFFICERS OF THE WISCONSIN ACADEMY OF SCIENCES,
ARTS AND LETTERS
President
H. A. Schuette, University oj Wisconsin
Vice Presidents
In Science: Ruth Walker, Milwaukee
In Arts: Walter Bubbert, Milwaukee
In Letters: Helen White, University of Wisconsin
Secretary-Treasurer
Banner Bill Morgan, University of Wisco7ist7i
Librarian
Halvor O. Teisberg, University of Wisconsin
Curator
Edward P. Alexander, State Historical Museum
Council
The President
The Vice-Presidents
The Secretary-Treasurer
The Librarian
E. A. Birge, past president
Charles S. Slichter, past president
L. J. Cole, past president
Charles E. Allen, past president
Rufus M. Bag g, past president
Paul W. Boutwell, past president
A. W. Schorger, past president
Committee on Publications
The President
The Secretary-Treasurer
Philo M. Buck, Jr., University of Wisconsin
Committee on Library
The Librarian
O. L. Kowalke, University of Wisconsin
Ruth Marshall, Wisconsin Dells
James F. Groves, Ripon College
W. N. Steil, Marquette University
Committee on Membership
The Secretary -Treasurer
E. F. Bean, Wisconsin Geological Survey
P. W. Boutwell, Beloit College
W. E. Rogers, Lawrence College
A. W. Schorger, Madison
TABLE OF CONTENTS
Page
Brule River Survey: Introduction. E. Schneberger and A. D. Hasler . „ 1
Topography and Geology of the Brule River Basin. E. F. Bean and
John W. Thomson, Jr . . . . . . . 7
A History of Fishing in the Brule River. D. John O’Donnell . . . 19
Vegetation of the Brule Basin, Past and Present. Norman C. Fas sett . . 33
A Survey of the Larger Aquatic Plants and Bank Flora of the Brule
River. John W. Thomson, Jr . . . 57
The Quail in Early Wisconsin. A. W. Schorger . . . 77
Small Mammal Censuses Near Prairie Du Sac, Wisconsin. Harold C.
Hanson . . . .105
The Lake Sturgeon, Acipenser Fulvescens Rafinesque, in Lake Winne¬
bago, Wisconsin. Edw. Schnebergkr and Lowell A. Woodbury . . . . .131
The Bur Oak Openings in Southern Wisconsin. A. B. Stout . . . .141
Some Aquatic and Sub-Aquatic Plants from the Region of Glacial
Lake Wisconsin. John Catenhusen . . . . . . .163
The Mosses of Wisconsin. L. S. Cheney and Richard Evans . . . . . .171
Notes on Wisconsin Parasitic Fungi. V. H. C. Greene . . . . , .225
Notes on Wisconsin Parasitic Fungi. VI. H. C. Greene . . . . . . 245
Preliminary Reports on the Flora of Wisconsin. XXXI. Boraginaceae.
Emil P. Kruschke . . . . . . . .273
Parasites of Northern Wisconsin Fish. Ralph V. Bangham ...... _ _ _ _ _ .291
Syrphid Flies of the Genus Cheilosia, Subgenus Chilomyia , in North.
America (Part II). C. L. Fluke and F. M. Hull . . ,327
Preliminary List of the Hydracarina of Wisconsin. Ruth Marshall, . . „B49
The Physaloptera (Nematoda) of Carnivores. Banner Bill Morgan . . .375
Winter Oxygen Content and Biochemical Oxygen Demand in a Wis¬
consin Artificial Lake. Charles H. Lewis and Neil E. Stevens . . . 389
Further Observations on Alkaline Flooding Water in Cranberry
Growing. Neil E. Stevens . . . .395
Studies of Silurian Fossils in the Thomas A. Greene Collection at
Milwaukee -Downer College. Katherine F. Greacen and John R. Bali,. ,415
Boron Deficiency in Beets as Correlated with Yields and Available
Boron. K. C. Berger and E. Truog . . . . .421
The Acidity of Honey. H. A. Schuette and Frank J. Schubert . . . . „ .427
Gasogens. C. V. Sweet . . . . . . .435
Professor Beatty’s Interpretation of Shakespeare. Julia Grace Wells . . 441
Racial Classifications of the Seventeenth and Eighteenth Centuries.
J. S. Slotkxn . . . . .459
List of Publications Dealing with Wisconsin Limnology, 1871-1945,
Chancey Juday and Arthur D. Hasler . . . . .469
Proceedings of the Academy . . . . . 491
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Doe, J. H. 1934. The ecology of Wisconsin. Trans. Wisconsin Acad. Sci.
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the Academy should be sent directly to the Librarian, Halvor O. Teisberg,
120 State Historical Building, Madison, Wisconsin.
iv
BRULE RIVER SURVEY: INTRODUCTION*
Brule River Survey: Paper No, 1
E. SCHNEBERGER
Biology Division , Wisconsin Conservation Department
A. D. Hasler
Department of Zoology , University of Wisconsin
The Brule River in Douglas County is one of Wisconsin’s
largest and most scenic streams. Its past fame as a trout stream
does not need elaboration as it suffices to state that even presi¬
dents of the United States were attracted to the stream to try
their luck. However, during the past few years the fishing has
declined even though heavily stocked and “improved” by the
installation of a large number of stream improvement struc¬
tures.
The need for an intensive study on this stream became evi¬
dent when it was realized that during a five-year period extend¬
ing from 1937 to 1941, a total of $34,247.67 was expended for
the planting of fish and that stocking was not bringing about
the desired results of maintaining or improving fishing.
It naturally follows that a well-balanced management plan
cannot be developed without knowing the factors which govern
the fish producing capacity of the stream. The purpose and ob¬
jective of the Brule River Survey may, therefore, be stated as
“the evaluation of the physical, biological, and chemical charac¬
teristics of the Brule River and its watershed so that an efficient
and well-balanced fish management plan might be developed
and placed into operation.” To this end the Conservation Com¬
mission sought the services of the scientists from the University
of Wisconsin and a co-operative research project was evolved.
A fund of $9,000 for a two-year study was established by the
* A co-operative project sponsored by the Wisconsin Conservation Deparmtent and the Uni¬
versity of Wisconsin. The results of the survey will appear in a series of papers that will be'
printed in the Trans. Wis. Acad. Sex. Arts & Let. Reprints of these articles will be made
available to interested parties upon application to the Wisconsin Conservation Dept., Madison 2.
1
2
Wisconsin Academy of Sciences , Arts and Letters
Conservation Commission and work began in September, 1942,
Owing to wartime difficulties — manpower shortage and travel
restrictions — many phases of the original plan could not be car¬
ried out in the expected detail. Nevertheless, the important
basic items have been subjected to analysis. The technical re¬
sults of the studies will be published in the Transactions of the
Wisconsin Academy of Sciences, Arts and Letters with a popu¬
lar interpretation of the results appearing in the Wisconsin
Conservation Bulletin. Publication will be in a series of scien¬
tific papers issued as rapidly as the studies warrant. Several
appear in this issue.
The Brule River is in many ways an ideal stream upon which
to conduct a broad detailed study. It is one of the few larger
streams that has not been altered by dams. It does not receive
sewage from industry or a municipality. It contains a variety of
ecological conditions. The upper section of the stream lies in a
boggy, marshy area and then broadens out into widespreads
approaching lake conditions. The middle section immediately
below the widespreads is a stretch of “fast” water containing
many rapids. The lower section continues as a stretch of rather
flat, quiet water and empties into Lake Superior. On the other
hand, the stream is too large for a complete study to be con¬
ducted during a two-year period with a limited personnel.
Some of the problems of general interest undertaken in this
study are as follows :
To determine the number of fish reaching the anglers" creel
a census was begun with the opening of the season, May 1, 1943.
Census clerks were stationed at the points where the concentra¬
tion of fishermen was the greatest. These individuals procured!
from the angler the number and species of fish caught, the
length, weight, and sex of each. Scale samples were collected!
which are later used to determine the age and rate of growth.
To interpret the efficiency of plantings of hatchery raised trout,
5,000 legal sized trout (brook and rainbow) were marked and!
placed into the Brule during the summer of 1943 and 7,00©
(brook trout only) in 1944. All fish planted during the course of
the study were marked and only trout of legal size were used.
The clerks recorded the marked trout in the creels and the data
from such returns will be compared with the original plant t©
determine the contribution to the creel. Recapture of marked!
Schneberger and Hosier— Brule River Survey: Introduction 3
trout in experiments conducted by the Conservation Department
and other states indicate that approximately 20 to 75 per cent
of spring and summer planted legal size fish are caught by the
anglers. In such studies it has been found that recaptures from
fall plantings are appreciably lower.
Rainbow and brown trout are exotic species while brook
trout were the original inhabitants of the Brule. Each of these
species has definite optimum requirements; therefore, a knowl¬
edge of their suitability to the stream must be the guiding factor
in its management. Consequently, this association was a case for
study. The rainbow trout in particular present some interesting
problems. It is apparent that most of the adults inhabit Lake
Superior, migrating up the Brule River in the spring to spawn.
Angling for the migrating fish furnishes the fisherman a great
amount of sport. It would be well then to learn more about the
life history of this species in the Brule.
To shed light on some of these questions, a weir has been
constructed at Stone's Bridge. This weir has a two-way trap
which is inspected daily by an attendant. The fish entering the
trap from upstream are fin clipped or tagged and transferred
over the weir and released downstream. Likewise, the fish enter¬
ing from downstream are also fin clipped or tagged and released
in the direction in which they were going. Information gathered
at this weir will provide data on brook trout biology. Recapture
of trout through this station will answer some of the questions
listed above. In addition, this trap will enable the biologists to
determine the number of other species (suckers, northern pike
and walleyed pike) that spawn or migrate in the Brule. An
experiment was also initiated to test the ability of brown trout
to maintain themselves without stocking.
As a trout stream, the Brule is peculiar because of the two
large “widespreads” (lakes) which are well suited for northern
pike. It is hoped that the findings will give a clue to the extent
that northern pike prey upon or are injurious to the trout popu¬
lation. These widespreads expose a greater surface of quiet
water to the warming rays of the sun, resulting in a higher
temperature in that area, consequently its effect on fish must be
studied.
The severe winter of 1942-43 created a problem because of
the formation of “anchor ice” on the bottom of the stream. It
4 Wisconsin Academy of Sciences , Arts and Letters
forms on the bottom during cold clear nights and rises subse¬
quently in the day because of the warming of the sun. It is pro¬
posed to learn the effect of this ice on the trout habitat because
it was noted that considerable quantities of rocks and debris,
in addition to the organisms attached to them, were lifted and
carried downstream.
In order to study the amount of fish that a stream will sup¬
port and at the same time yield a moderate crop to the angler,
estimates are being made of the quantity of food organisms
found on various types of bottom in the Brule. Because trout
feed extensively in the summer on terrestrial insects (those
which have fallen in from overhanging vegetation), the biolo¬
gists are measuring the value of streamside cover in fish food!
production. These findings will be correlated with the variety
of organisms found in the stomachs of fish which the creel cen¬
sus clerks procured from the angler's creel. The rate of growth
of resident and marked trout will also be correlated. In addition,
density of trout population in various sections of the stream will
be measured by means of electrical anesthesia. The population
density can be then correlated with the success of the creel and
with the chemical and biological conditions.
Historical records and accounts of residents of the Brule
emphasize the detrimental effect of denuding the cover. Through
an intensive study of the cover of the watershed the plan is to
quantitate this effect. One of the co-operators compiled maps
based upon records of surveyors who tramped the section lines
of the Brule watershed in 1840. These maps will give an esti¬
mate of the concentration of timber of that period which can
then be compared with the present stand. Another compiled!
figures of the measurements of timber from aerial photographs
and corroborated these by observations in the field. This study
converts the impression of the lay observer into definite num¬
bers. Because the cover of a watershed influences the conditions
of erosion and the amount of water flow by springs and runoff,
it is felt that this information will give data which will be an aid!
in recommending procedures for improved cover conditions on
the watershed. Still other investigators are studying the erosion
on the river banks, from the many highways and roads and!
from farm land.
The general overall supervision and planning of the project
Schneberger and Hosier — Brule River Survey: Introduction 5
was the responsibility of the authors. D. John O’Donnell, biolo¬
gist of the Wisconsin Conservation Department operating from
the Conservation Department Biology Laboratory at Spooner
and the Brule Ranger Station, was in charge of all field opera¬
tions with W. S. Churchill and J. R. Jacobson as permanent
assistants. Temporary assistants were L. D. Prey, Helen Hall,
and Curtis Austin. Wholehearted and unselfish aid and coopera¬
tion have been received from many sources and the authors take
this opportunity to express their thanks to the multitude of
persons who in one way or another assisted in the project.
Thanks are especially due to N. C. Fassett, Professor of Botany,
University of Wisconsin, and John W. Thomson, Superior State
Teachers College, and now of the University of Wisconsin, who
conducted studies on the vegetation in the stream and on the
watershed; R. I. Evans, Department of Botany, University of
Wisconsin, who made studies of the origin of the bottom sedi¬
ments of plant nature ; F. C. Christopherson, Keith S. Brigham
and Robert H. Brigham, U. S. Geological Survey, who offered
important aid in the construction of instruments to measure
stream flow and their maintenance ; and E. F. Bean, State Geolo¬
gist, who restudied the geology of the Brule, in addition to organ¬
izing a soil erosion team (M. F. Schweers, Soil Conservation
Service and 0. R. Zeasman, University of Wisconsin) to study
the erosion problems arising from the stream banks, roads and
farmland.
Others who gave conspicuous service and who helped un¬
selfishly were J. E. Hanson, in charge of the Brule Ranger Sta¬
tion, and his dispatcher, Wm. Johnson ; J. W. McNaughton, con¬
servation warden, E. Lambert, H. Swanson, J. G. Ordway of
Cedar Island, and L. P. Jerrard who explored the Brule and
drafted a map valuable to the study.
E. J. Vanderwall, Conservation Director, Ernest F. Swift,
Assistant Conservation Director, and H. L. Russell, Chairman
of the University of Wisconsin Lakes and Streams Committee,
helped extensively in the arrangements for procuring services
and materials from experts and departments of their respective
organizations. Without their insight and willingness to act
promptly, the project would have lacked many of its broad
aspects.
TOPOGRAPHY AND GEOLOGY OF THE BRULE
RIVER BASIN
Bride River Survey: Paper No. 2
E. F. Bean and John W. Thomson, Jr.
Geological and Natural History Survey; Department of Botany ,
University of Wisconsin
As is the ease with several other streams rising in northern
Wisconsin the Brule River does not have the profile character¬
istic of a stream in a semi-mountainous region. Instead of a
curve which is flat near the mouth and steeper toward the source
the gradient is very gentle in its upper reaches and steeper
down stream. (Fig. 1) It rises in the boggy bottom of a mile¬
wide trench one hundred feet below the level of the sandy Bar¬
rens. The bog is so flat that the divide between the Brule and
the St. Croix is indistinguishable.* Rising at an elevation of
* Following are approximate elevations of the river: ,
1. Stesne’s Club House, Sec. 36, T.46N., R.11W . 1016
2. St. Louis Club House, Sec. 18. T.46N., K.10W . . 1013
3. McDougal’s Club, Sec. 3, T.46N., R.10W . 995
4. River at USH 2 at Brule . . . 941
5. Near center of Sec. 26, T.48N., R.10W . . 917
6. Near NV4 comer of Sec. 26. T.48N., R.10W . 895
1. SEy4 NEy4 22, T.48N., R.10W . 845
8. Johnson’s Bridge . 817
9. 100 feet N of S line of Sec. 10, T.48N., R.10W . 765
Lake Superior . . 602
Nos. 1-3 House Executive Document 330, 54th Congress, 1896.
Nos. 4, 5, 7 and 8 Wisconsin Geological Survey.
Nos. 6 and 9 House Document 227, 72nd Congress, 1st Session, 1930.
7
8
Wisconsin Academy of Sciences , Arts and Letters
Figure 2. Geological map of the Brule River drainage area.
Bean and Thomson — Topography of the Brule River Basin 9
1,022 feet the stream flows northward to Lake Superior. The
Copper Range (Fig. 2) which rises to a height of over 600 feet
above the lake is the most conspicuous feature of the drainage
basin.
The total fall of 420 feet in the air-line stream length of SO
miles can be divided as follows :
Fall in ft. per ■ mile
3
17
17
Fall in feet
Miles
30
5
14
92
85
243
Source to Copper Range
Copper Range
Sandstone
The actual length of the stream is increased by the numerous
incised meanders from an air-line length of 30 miles to 49 miles.
In the upper section much of the fall is in the Dalles in section
15, T.46N., R.10W. and in the rapids above the mouth of Ne-
bagamon Creek. Much of the descent across the trap series is in
the lower mile. In the sandstone section there are numerous
small falls and rapids. The descent in the first 2% miles below
the Copper Range is 80 feet.
With a drainage area of 190 square miles, the average width
is a little over 6 miles. At the Copper Range the width is but
4 miles. Near Lake Superior the width of the drainage area is
less than one mile. Some of the higher elevations are: on the
Copper Range near Maple, 1,240 feet; glacial hills southwest of
Lake Minnesuing, 1,280 feet ; and southeast of Brule, 1,260 feet.
The divide south of the Range has a maximum elevation of 1,280
feet and an average, except for the col near St. Croix Lake, of at
least 1,150. The average descent from the divide to the river
is about 200 feet. The river flows in a deep valley ; hence much
of the descent is near the stream. At the Range, the trap rises
220 feet in three-fourths of a mile. Near Brule, the valley depth
is about 100 feet.
Having such a narrow drainage area, it is not to be expected
that the Brule should have either long or numerous tributaries.
The Little Brule rises less than a half mile from the Brule and
flows northerly in what may have been a former channel ©f the
main stream to join the Brule near Brule village. Nebagamon
Creek rises a short distance northwest of the Brule-St. Croix
col and flows north and northeasterly to join the Brule near
Winneboujou. It drains Minnesuing, Steele, and Nebagamon
lakes, as well as large areas of swamp. North of the Range, the
lake clay plain slopes northward at the rate of about 40 feet per
mile. It is deeply dissected by small tributary streams.
10 Wisconsin Academy of Sciences , Arts and Letters
Geology
Two geological systems are found in the basin — Keweenawan
and Pleistocene. There is no evidence of the existence of any
rocks belonging to the intervening period of about a half billion
years,.
Keweenawan
This period began with the deposition of sediments, inter¬
rupted by the outpouring of lavas from extensive fissures. These
lavas flowed southward over parts of Wisconsin and Michigan
and northward over parts of Ontario and Minnesota, indicating
that the highest part of the region and the source of the lavas
were located near the present center of Lake Superior. The
total thickness of these flows exceeded 20,000 feet. As thousands
of cubic miles of molten material were withdrawn, there was
downwarping forming a structural basin or syncline. In this
basin there was accumulated a great thickness of sediments
derived from the upturned margins of the syncline. The most
conspicuous of these was the Great Conglomerate. Following
this was the last of the lavas known as the Lake Shore Traps.
Upon the Lake Shore Traps were deposited upper Keweenawan
shale, conglomerate and sandstone.
The only rocks outcropping in the Brule basin are Middle
Keweenawan traps and the Upper Keweenawan sandstone (Fig.
2) , which occupy the north limb of the northeast-pitching syn¬
cline whose axis extends southwesterly from Chequamegon Bay.
The lava flows vary in thickness from a few inches to several
feet. Trap is the name used for a dark igneous rock. Basalt is a
dark colored, fine grained trap rock. Diabase is a dark rock,
coarser in texture than a basalt. From the exposures on the
Amnicon and Middle rivers, it is inferred that the contact on the
Brule is a thrust fault which resulted in bringing of the older
igneous rocks up over the younger nearly horizontal sandstone,
with the plane of the fault dipping about 38° to the south (Fig.
3) . The flows strike N.65° E. and dip SE 40°.
Thwaites estimates that the displacement along the fault
plane was from 6 to 12 miles. No rock exposures along the Brule
show the fault contact between the sandstone and trap, but mag¬
netic readings and outcrops of sandstone to the north and of
trap to the south show that the fault is about one-half mile south
Bean and Thomson — Topography of the Brule River Basin 11
Vertical scale -feet
Figure 3. Cross-section of the Brule River drainage area.
of Johnson's Bridge in section 22, T.48N., R.1GW. Topographi¬
cally, the fault can be identified by the steep 200 to 800 foot rise
of the north face of the trap ridge from the plain to the north.
Magnetic readings indicate that the trap is from 8 to 4 miles in
width (Fig. 2). With but one exception the outcrops are con¬
fined to the ridge, about a mile in width, south of the fault. The
only outcrops in the river are in the SW1/^ of Section 28, T.48N.,
It. 10W. This ridge is called the Copper Range because both
native copper and copper sulphides have been found along this
entire range. The Percival location in section 27 is the best
known prospect. In section 31, T.46N., R.11W., there are two
outcrops of diabase dipping southward about 15°.
Sandstone exposures are numerous along the Brule River
from about % mile south of Johnson's Bridge to Lake Superior.
The sandstone is flat-lying, the dip to the south varying from
0° to 3°, except near the fault, where some beds dip north at an
angle of 20°. These beds are probably upturned slightly by the
thrust faulting. Although no rock is exposed in the basin south
of the Copper Range, it is certain that the underlying rock is
upper Keweenawan sandstone dipping southerly at a low angle.
The upper nine miles of the Brule's course is parallel to the trend
of the syncline.
The relief prior to glaciation was much sharper than at pres¬
ent, due both to the degradational effect of the ice and to the
mantle of glacial drift which tended to fill depressions. The
Copper Range was even more conspicuous than at present. To
the north and south were Keweenawan sandstone lowlands.
12 Wisconsin Academy of Sciences, Arts and Letters
Pleistocene
There were probably several invasions of ice, the latest of
which moved in a general southerly direction and is responsible
for the soils of the area. The ice sheet must have reached a con¬
siderable thickness before it overrode the Copper Range and
moved on southward. It was, therefore, able to erode the sand¬
stones and to do a considerable amount of smoothing and pluck¬
ing of the trap ridges. At the time of maximum advance, the ice
was thinnest over the Range and thicker both to the north and
south. As a result of this, when forward movement of the ice
ceased, the Range was the first to emerge, leaving stagnant ice
masses to the south and the large Superior lobe of ice in the low¬
land to the north.
When the ice finally disappeared, there were left in the drain¬
age basin four types of glacial deposits: (1) terminal moraine,
(2) outwash, (3) glacial drift modified by lake action, and (4)
lake clay. (Fig. 4)
1. Terminal Moraine . There is no continuous belt within the
drainage area that might be classed as recessional or terminal
moraine built at the stationary front of the ice sheet. Instead
there are isolated areas with considerable local relief and knob
and sag topography. The occurrence of boulders in the channels
of the Brule indicates that ground or terminal moraine deposits
were buried by outwash sand and gravel and later exposed and
concentrated to a boulder pavement by stream erosion. The
larger boulders which cover the valley floor at Cedar Island indi¬
cate that the area of terminal moraine around the fire tower in
section 13, T.46N., R.10W. was originally connected with the
terminal moraine across Brule Valley to the west. Terminal
moraine belts together with stagnant ice masses constituted the
southern border of Glacial Lake Duluth.
2. Outwash. Extending southwesterly from northern Bay-
field County for over one hundred miles is a sandy belt from
5 to 15 miles in width, which has long been called “the Barrens.”
Much of the Barrens should be classified as pitted outwash, the
pits being formed by the burial and subsequent melting of ice
blocks. That these pitted areas are outwash rather than termi¬
nal moraine is shown by the fact that the summit levels are
relatively uniform, that boulders are not numerous, and that
Bean and Thomson— Topography of the Brule River Basin 13
Terminal Moraine
P^lOutwash
Ev^LakeClay
■Rock Controlled Highlands
I _ Idacial LakeDuluth and
outlets
T.49N
T.48N.
Outlet
_Lake
Ashland
T.47N.
T.46N,
T.45N.
R.IIW. R.IOW.
Figure 4. Glacial geology of the Brule River drainage area.
14 Wisconsin Academy of Sciences , Arts and Letters
cuts show well-stratified sand and gravel. Much of this material
came from the interlobate moraine to the northeast. It is nat¬
ural in an area so largely underlain by friable sandstone that
the glacial drift should be sandy and that the glacial streams
should build sandy outwash plains. The general level of “the
Barrens” is about 1,180 feet. Along the Brule there are terraces,
indicating that sand and gravel was deposited by streams flow¬
ing away from the melting ice and later dissected by outwash
streams or by outflow from the glacial lakes. Near the source
of the river, in section 34, T.46N., R.11W., the first bench, which
is about 100 feet above the swampy valley floor, is at 1,120 feet
and is less than one-half mile wide. The second bench is also a
little less than one-half mile wide, has an elevation of 1,160 feet*
and ends in a steep terrace which rises about 20 feet to a third
bench at 1,180 feet, which is not so well defined.
3. Glacial Drift Modified by Lake Action . A guess can be
made as to the landscape prior to the development of the first
glacial lake. Ice blocks may have still filled depressions now
occupied by lakes. Water from the melting ice accumulated be¬
tween the margin of the ice lobe in the Lake Superior basin and
the divide to the south, forming glacial lakes, with levels de¬
termined by the elevation of low points in the surrounding high¬
land. It is probable that stagnant ice masses as well as land may
have formed part of the barrier. Glacial Lake Duluth began as
a string of small marginal lakes on the border of the ice lobe.
Upon further shrinkage of the ice, these lakes became confluent.
This lake stood at three different levels, the highest being 1,160)
feet, and the lower ones, in order 1,120 and 1,060 feet. These
lake levels are reflected in (1) large flat areas produced by the
erosion and deposition of relatively shallow water; (2) beach
lines; (3) wave-cut cliffs; and (4) terraces cut by outlet streams.
It is quite likely that outwash streams continued to deliver sedi¬
ments to “the Barrens” while the glacial lakes were in existence.
At the 1,160 level, an arm of the lake covered the area now occu¬
pied by Lake Nebagamon and Lake Minnesuing, with drainage
south from the latter lake. That such a course was possible is
indicated by (1) the present level of Lake Minnesuing, about
1,132, draining by sluggish Minnesuing Creek to Lake Nebaga¬
mon; (2) a valley extending southward from the south end of
Lake Minnesuing to the present Brule valley drained for all but
Bean and Thomson — Topography of the Bride River Basin 15
a mile of its length by Wilson creek. The topography indicates
that another arm of the lake extended south past Winneboujou
and drained to the southwest, leaving the intervening higher
land as an island.
Due to the cutting down of the outlet, or retreat of the ice,
the lake level fell to 1,120 feet, and later to 1,060 feet. At each
of the new levels the Brule adjusted its channel and developed a
terrace faced by a steep slope. There is an abandoned tributary
stream channel in sections 25 and 26, southeast of Brule, that
formerly drained northwest. Its banks are very steep and ex¬
pose sand and gravel. It probably received drainage from melt¬
ing ice to the east. The channel at the mouth is at the 1,060 foot
level, suggesting that it flowed into Lake Duluth at that level.
Similar channels enter the valley from the east in T.46N., R.10W.
It is difficult to determine the exact outlines of the lake at the
various stages because topographic maps are lacking for critical
areas, and because the amount of post-glacial uplift has not been
determined. Leverett states that “the head of the outlet now
stands about 250 feet higher than at the time when the lake dis¬
charged through it.” Hansell, using more complete information,
has estimated the uplift of the head of the valley to be between
50 and 60 feet. Using his data, the uplift at the mouth of Brule
was only 20 feet more than at its source. If this is true, tilting
is not of importance in consideration of Brule River history.
When the level of the glacial lake dropped below 1,022 feet,
the direction of flow of the Brule was reversed and the stream
flowed north into the glacial lake instead of draining it. This is
supported by the fact that the stratified deposits in the river
above that level dip south, while the bedding dips north in de¬
posits below the 1,020 foot level. With flow to the north, in spite
of greatly reduced volume, the Brule River was able to incise its
channel and cut a gorge in lake deposits below 1,020 feet.
On the north side of the Copper Range, there is a 980 foot
bench. Below 980 feet to the present lake shore the soil is domi¬
nantly red clay deposited in the bottom of the glacial lake.
The transition from Lake Duluth to Lake Algonquin was
probably a gradual one as lower and lower passages for drain¬
age across the Upper Peninsula of Michigan were opened by the
melting away of the ice in the eastern part of the Lake Superior
basin. There was a brief period when the flow of Glacial Lake
16 Wisconsin Academy of Sciences , Arts and Letters
Duluth was southward through the Au Train-Whitefish Valley
to Glacial Lake Chicago. The Lake Algonquin beaches are weak
and widely spaced. As a result of the successive lake levels, a
great deal of the drainage basin south of the red clay belt has a
greatly modified topography. Glacial lake beaches and wave-cut
cliffs are striking features but cover a relatively small area.
The effect of the glacial lake was to subdue the topography.
Depressions were filled and elevations planed down. The coarser
material was shifted the least ; hence boulder concentrates char¬
acterize the flat uplands, sand lies on the slopes, clay was moved
farther and deposited along the foot of slopes and in depressions.
Ground moraine, with little initial relief, was smoothed to a fiat
or swamp area. Terminal moraine below lake level was smoothed
but retained some of its original knobs and sags. Outwash
plains, if not pitted or dissected, exhibit little change.
4. Lake Clay. Heavy red lake soil extends from the Copper
Range north to Lake Superior. Along the Brule valley, the clay
extends four miles further south to Brule. Well records indicate
lenses of sand and gravel extending northward, dipping at a low
angle and separating beds of clay. These water-bearing lenses
are at shallow depths near the Copper Range, but several miles
farther north are at a depth of one or two hundred feet.
Post Glacial Changes
The clay belt has been deeply trenched by narrow, steep¬
sided valleys which range from a few feet to over a hundred
feet in depth. This is in marked contrast to sandy Barrens farth¬
er south, where the water sinks into the sand and erodes but
little. In the areas of terminal moraine and of drift modified by
glacial lake action, there is some gullying on the steeper slopes.
Ground Water
In the clay belt, direct runoff is heavy because the clay is
relatively impervious and the swamps provide relatively little
surface storage. The conditions in the drainage area above the
clay belt are favorable to uniform stream flow. The Barrens are
a perfect source of stream supply because the sand acts as a
sponge, absorbing a high percentage of the rainfall, and de¬
livering it to the stream in numerous springs at a uniform rate.
We believe that the springs are due to boulder clay covered by
Bean and Thomson — Topography of the Brule River Basin 1.7
sand and gravel. Water falling upon the surface descends to the
more imprevious material which it follows until an outlet is
found. The headwaters, therefore, have a relatively constant
flow. The glacial drift, modified by lake action, has large areas
of swamp which serve as reservoirs. Runoff is retarded on the
extensive flat areas. In the terminal moraine much of the rain¬
fall is held temporarily in the kettles. The lakes also serve to
retard runoff. Precipitation in the winter months generally falls
in the form of snow and usually has slight effect on stream flow
during that period.
“Effect of ground storage and springs on stream flow . The
flow of the Brule River is subject to less fluctuation than that of
any other stream in this district, the lowest observed flow being
118 second-feet and the highest, 1,490 second-feet. The natural
regulation is due primarily to the yield from a number of large
springs situated along the south branch or Upper Brule River.
These springs vary in area from one-quarter of an acre to three
acres, and are about 5 or 6 feet in depth. In the bottom of most
of the lakes or springs there may be seen, boiling up through the
sand gravel, jets of water varying from one inch to as much as
10 feet in diameter. The water flows are remarkably high for
this district.”*
House Document 227, 72nd Congress, 1st Session, 1930, p. 16.
A HISTORY OF FISHING IN THE BRULE RIVER
Bnde River Survey: Paper No. 8
D. John O’Donnell
Wisconsin Conservation Department
Biology Division
The famous Brule River, located approximately 30 miles
east of the city of Superior, in the northwestern part of Wis¬
consin, is one of the better known of the important trout streams
in the United States. Owing to the fact that the trout popula¬
tions have apparently declined since the days of lumbering op¬
erations, it was deemed desirable to make a complete physical,
chemical and biological investigation of the Brule River, with
the aim of establishing a stream management program for the
river. The investigational work started in October of 1942 as a
cooperative project between the Wisconsin Conservation Com¬
mission and the University of Wisconsin. It was first necessary
to review the literature and determine the known facts concern¬
ing past conditions in the river. The present report is a short
resume of the history of the Brule River valley, with the stress
placed principally upon the fish and fishing conditions.
The very earliest history concerns the changes in the river
during geological times. Since any geological history is con¬
cerned primarily with physical changes, these aspects are
omitted and will be covered in a subsequent report on the geology
of the Brule River valley.
The more recent history of the Brule River valley begins
necessarily with the story of the Indian. The earliest record is
that of the Mound Builders, who apparently had an advanced
type of culture and were proficient in the metal arts. They mined
copper in what is now known as the Minong Range and at Mani-
tou Falls on Black River, and used both fire and water in mining
the metal. The copper was worked into various weapons, imple¬
ments and ornaments and when one of their number died, vari¬
ous copper pieces were placed in the mound with the body. These
19
20 Wisconsin Academy of Sciences , Arts and Letters
Mound Builders vanished completely before the year 1400 A. D.
The next group of Indians, of which we have any knowledge,
were the Mascoutins, “People of the Fire,” a branch of the Pota-
watomi, who lived by trapping beaver, harvesting the wild rice,
spearing whitefish and hunting deer. About 1400, the Dacotah,
“The Seven Council Fires,” left their homes in what are now
known as Virginia and North Carolina, and trailed the bison
westward and came to Wees-kon-san. The Dacotah drove out the
peace-loving Mascoutins. The next large tribes were the O-dug-
am-eeg (Outagamie), and the O-saug-eeg (Sauk) tribes which
were forced westward by the Iroquois. These three tribes shared
the wild rice lakes around the the Bois Brule-St. Croix head¬
waters. They also trapped beaver and other small animals.
About 1400 A. D. the Ojibwa Indians migrated westward,
being forced out by the Iroquois. They moved very slowly but
eventually reached what is now known as Sault Sainte Marie,
where they established their principal village. Even here they
were attacked by the Iroquois so they continued to move west¬
ward. In 1492 they reached Shan-ah-waum-ik-ong (Chequa-
megon Bay) where they engaged in battle with the Dacotah and
Outagamie tribes, who forced them to move off the mainland
and withdraw to Mo-nung-wah-na-can-ing (now Madeline Is¬
land). They built a village on the island and planted maize and
pumpkins. All of their hunting for game was done on the main¬
land. These hunting excursions into their own territory so
alarmed the Dacotah and Outagamie tribes that they engaged
the Ojibwa tribe in an immense battle during the year 1612.
The Ojibwa, however, won the battle and gained a foothold on
the mainland, thereafter spreading to the south and west. As
they moved westward they again fought the Dacotahs for control
of the rice lakes and the small game hunting about the Bois
Brule, which they called the Wa-sah-que-da-ce-be, “Burnt
River.” This peculiar name, “Burnt River,” must have been used
because of some notable forest fire or fires in its valley, before
the day of the white man.
By 1620, the Ojibwa tribe had control of most of the territory
but about this time the Sioux tribe moved into the area and many
fierce battles were fought, until a truce was effected in 1671.
After 1671, the two tribes collaborated in their hunting of small
animals and in the harvesting of wild rice from the lakes. The
O'Donnell — Fishing in the Brule River
21
Ojibwas carried furs from the Brule valley to the French on the
St. Lawrence in eastern Canada.
An account of the discovery of the Brule River has been given
by Francis Parkman, who was called by Eancroft “the greatest
American historian.” He narrated that, “Daniel Greysolon Du-
Lhut, in June 1680 while Hennepin was in the Sioux villages,
set out from the head of Lake Superior, with two canoes, four
Frenchmen and an Indian, to continue his explorations. He
ascended a river, apparently the Burntwood and reached from
thence a branch of the Mississippi which seems to have been the
St. Croix.”
In DuLhut’s own words he recorded in his journal in June,
1680, “not being satisfied with my explorations by land, I took
two canoes with a savage who was my interpreter, and with four
Frenchmen, to seek the means of making it by water. [Referring
to a trade route into the Northwest]. For this purpose I entered
into a river which has its mouth eight leagues from the ex¬
tremity of Lake Superior on the south side, where after having
cut down some trees and broken through about 100 beaver dams,
I went up the said river, and then made a carry of half a league
to reach a lake which emptied into a fine river which brought me
up to the Mississippi.”
In 1698, Pierre LeSueur was dispatched by authorities of
New France to keep open and protect the old route through the
Brule and St. Croix Rivers. He built a fort on Madeline Island
to guard the north approach and another on an island in the
Mississippi, below the mouth of the St. Croix and near the town
of Red Wing, Minnesota, to guard the southern approach.
Jonathan Carver, the first English traveler in Wisconsin,
portaged from the St. Croix to the Brule River and descended to
Lake Superior. He reported a number of beaver dams. How¬
ever, in another period of his travels he says “this river was so
scant of water we were obliged to raise it with dams for pas¬
sage.” His trip was made in July, 1767. Incidentally Carver re¬
named the river Goddard’s River for an early fur trader.
In 1782, Jean Cadotte used the Brule-St. Croix route. The
stream was hard to navigate owing to the beaver dams.
In 1808-04 Michel Curot, a fur trader, established trading
along the Brule and St. Croix Rivers. He carried on intensive
trapping of beaver and the river was cleaned of beaver and many
22 Wisconsin Academy of Sciences t Arts and Letters
dams were destroyed. No mention was made of seeing any fish.
His first trip up the Brule River started on August 23, 1803 and
the first day he traveled as far as the end of the first decharge.1
The next five days were spent in navigating the first three
decharges. During the next three days, travel was much easier
and the party reached a point which they called La Grande
Prairie.2 3 The next day the party continued and passed what they
called the first rapid. They moved through an area of quick
water but no rapids and passed what is now known as Little Joe
Rapids. Two days later they had arrived at a place which Curot
called the “Rapide a Vassel.,,3 During the next day rapid pro¬
gress was made in the flat quiet water and a point was reached
a league and one-half below the St. Croix portage. On Septem¬
ber 5, the passage up the Brule had been completed and the party
started the portage over into the St. Croix. A total of twelve
days was required for the trip from the mouth of the Brule to
the point of portage into the St. Croix.
One of the first Americans to visit the stream was Henry
Rowe Schoolcraft, who was an Indian agent at Sault Sainte
Marie. In 1831, his party came to the Brule and was guarded by
Lieutenant James Allen of the Fifth United States Infantry
with a number of troops. Schoolcraft speaks of moose hunting
on the Burntwood River, while Allen says 'The river is exceed¬
ingly cold and clear and is filled with thousands of real mountain
brook trout/' Allen had hard work descending the stream with
awkward soldiers who were unaccustomed to guiding canoes in
strong water. “Often,” says Schoolcraft, “on looking down its
channel there are wreaths of foam constituting a brilliant vista.
This stream might appropriately be called Rapid or Mad River.”
Schoolcraft made no mention of beaver dams and apparently
they had disappeared because of the thorough trapping of Michel
Curot. Schoolcraft was the first to mention trout in the river.
According to the records of the earlier explorers the river con-
1 A decfaarge indicates a place where it is necessary to portage. The first decharge was about
three miles above the mouth of the Brule. The bed of the river at this point was solid brown
sandstone and the place is now known as Gregory Falls.
3 Properly speaking there are no prairies on the Brule. This camping area is supposed to have
been on the eastern bank above the mouth of the Little Brule River where the banks are somewhat
fiat.
3 Above what is now known as Nebagamon Rapids, the river expands into a number of lakes.
Cochran’s, Spring, Lucius, Big and Sucker. Falls Rapids, above Sucker Lake, although very short,
are considered the hardest on the upper river, and these are probably what Curot called “Rapide
a Vassel.”
O'Donnell— -Fishing in the Brule River
28
tained hundreds of beaver dams but no fish, although most of
them referred to fish in the St. Croix waters, especially in Lake
St. Croix.
From the time of the earliest Indians to the period of School¬
craft the river had been called by many names : Nemitsakouat,
Wisakoda, Bois Brule, Burntwood, Goddard, Brule and Mad
River.
In 1846, John R. St. John was charting the country in the
interest of mining companies and wrote a report on “A True
Description of the Lake Superior Country.” He writes of the
Bois Brule : 'The shore of the river is a sandy alluvium, as the
rivers Montreal and Ontonagon, with the red sand rock, and the
country of the Brule has the same general characteristics after
leaving Great Lake Point, that marks the country of the Ontona¬
gon, and the river itself, after leaving Keweenaw Point. Its
mouth is thirty to fifty feet wide, sandy, and five feet of water
on the bar. It surpasses all other streams in its brook trout,
some of them, I have the assurance of Mr. Jacob, weighing ten
pounds. Its waters colder and clearer, if possible than any other
river.”
In 1874, a Mr. R. P. Petre of Baltimore with his party,
fishing the Brule, removed the barbs from their hooks because
the trout were so easily taken that the time spent in removing
the hooks from the mouth of the fish was considered time wasted.
Mr. John Bardon of Superior, in the winter of 1877, saw “mil¬
lions” of trout swimming under the clear ice of the Brule. He
cut a hole through the ice and netted 1,500 pounds of trout with¬
out seemingly depleting their numbers. In 1878, “Long John”
Murphy and his companion reported catching 500 trout by hook
and line in three days.
In 1880, a prominent manufacturer, Samuel Budgett of Bris¬
tol, England, conceived the idea of improving the condition of
some of his better employees. He purchased a large area .of land
at and near the mouth of the Brule River. He then selected
approximately thirty families, representing various trades,
brought them from England and started the first white settle¬
ment at the mouth of the Brule. He named the colony “Cl eve-
don.” The harbor at the mouth of the river was improved and
fishing boats, nets, cooperage equipment and a sawmill were
provided. Small farms were opened up and although the settlers
24
Wisconsin Academy of Sciences, Arts and Letters
were a sturdy lot they were not successful and after a number
of years a great many left and the colony disintegrated.
In a report by E. T. Sweet on the Geology of the Western
Lake Superior District, published in 1880, the following descrip¬
tion is given of the upper part of the Brule River :
^About four or five miles above the dalles on Sec. 30,
commence the Upper Spring lakes. These lakes extend to
within a mile of the dalles, and are usually merely former
channels of the river. There are somewhat more than a
dozen of them, each covering from three acres to a quar¬
ter of an acre. They are usually parallel to, and on the
east side of, the main channel. They are not often more
than five or six feet deep, but the water is very clear, and
in the bottom of most may be seen jets of sand and fine
gravel continually boiling up, varying in size from an
inch to five or even ten feet in diameter. In passing over
the surface of some of the larger lakes in a canoe, from
fifty to a hundred of these springs may be counted. In
these lakes are the breeding grounds of the vast numbers
of brook trout that inhabit the upper waters of the Brule.
I have seen them, upon a clear day, in these lakes, as
thick as minnows in a common pond. The bottom of the
stream above these lakes, and of the much larger lakes
immediately below them, contain a deep, loose black mud,
filled with insects and worms, the favorite food of the
trout. It has been aptly said that this is the angler’s para¬
dise. One may capture in a short time all that he can
carry. Joseph Gheen, a half-breed Indian, has recently
built a cabin upon Sec. 21, near the lakes, from which
point he takes the fish during the winter months to Du¬
luth and Ashland. About a mile below the Spring lakes,
swift rapids are found about two hundred yards in length,
and near the termination the river is only seven or eight
yards wide. The fall of the river here is about fifteen feet,
and the place is known as the Dalles of the Brule. The
banks are of clay and boulders only, and seven or eight
feet high. At the foot of these rapids is the third Puc-
wagawong [Chippewa Indian— a place where reeds or
flags grow] or Flag lake. It is only 250 yards in length
and perhaps 150 in width. From the foot of the third to
the head of the second Flag lake there are rapids of not
more than a hundred yards in length. The latter lake is
a mile in length and from two to four hundred yards in
width, with a depth of three or four feet. The bottom is
very muddy, and it is said that during the summer, reeds,
grasses, and moss form an almost complete mat over the
surface of the water.”
O'Donnell — Fishing in the Brule River
25
The lakes referred to as having boiling springs and as being
the breeding grounds of the brook trout consist of the spring
ponds which were bought by Henry Clay Pierce and fenced off
from the river proper some time shortly after 1905. It is inter¬
esting to note that the widespreads which are now known as Big
Lake and Lucius Lake were reported as having a mud bottom
and becoming choked with aquatic vegetation during the summer
months.
About 1880, the Brule River valley was opened for travel.
Railroads and wagon roads were built and the river was becom¬
ing known as an excellent fishing area. Trout were reported as
plentiful, and all fishing was done from canoes and boats. About
this time articles began to appear occasionally in the Superior
papers with reference to the Brule River and the trout.
In June, 1884, it was reported that the trout fishing in the
Brule River was excellent. In May, 1885, there appeared an
article which stated that no finer trout fishing can be found any¬
where than can be found in the Brule. Speckled trout twenty-
four inches in length have been taken from this stream. The
principal fishing grounds, from the town of Brule, were up the
river about five miles by road, and about eight by river. These
grounds are above the lower rapids and extend about six miles
to the upper rapids. This is considered the best fishing area on
the river, although there are trout in all parts. The bottom is
sandy and rocky and the water is clear, cool and sparkling. The
banks rise gradually from the river and are covered with gigan¬
tic pine trees. In one report of a party of three fishermen they
state that in one day's fishing they caught 100 speckled trout and
that on the next day they caught an additional seventy-four, one
of which was sixteen inches in length. The trout were jumping
out of the water in all directions.
In 1892 the village of the town of Brule was platted. The
iownsite was owned by a group of central and southern Wis¬
consin lumber operators. The business and other activities of
the town were controlled by the Brule Lumber Company, whose
holdings consisted of over 3,000 acres in the Brule valley, which
was considered the richest and most dense timber district of
northern Wisconsin. It was estimated that the company cut ap¬
proximately fifty million feet of logs as a minimum. In the win¬
ter of 1892 about four million feet of logs were cut.
26 Wisconsin Academy of Sciences , Arts and Letters
In an article dated 1893 it was stated that, “along the Brule
River which flows through the Town of Brule, the timber is very
heavy and is of a very superior quality. The Brule River is a
beautiful stream and is celebrated for its trout fishing. Some of
the finest specimens of trout ever hooked in the Northwest have
been taken from these waters and as a result the river has
gained a general celebrity for its beauty and limitless fishing re¬
sources.”
In October of 1894 an article was "written giving a resume of
the season, as follows :
“The steamer North West has brought many eastern
people to the Brule, and has largely increased the number
of campers. It is estimated that nearly a thousand people
have encamped on the upper Brule this summer. Taking
the clubhouses in their order, going up the river to-wit:
St. Paul or Winneboujou clubhouse, 50; Milwaukee or
Gitche Gurnee clubhouse, 30; Ashland or Missishin, 50;
Lucius (public clubhouse on McDougalPs land), 300; Tib-
bits camp (public), 60; Kline’s of Duluth, 10; St. Louis,
22 ; White Birch, 50. This range of clubhouses extending
along the river, from the St. Paul clubhouse on the north
near the D. S. S. & A. tracks, south fifteen miles to the
White Birch clubhouse near the Omaha railroad, covers
practically, the fishing grounds of the Brule. The fishing
laws ought to be further modified to prevent shipping at
any season. One party shipped over 2,700 trout to Su¬
perior this summer, supplying three restaurants. Over
sixty campers were on the grounds as early as May.”
In 1895 the following notes were published with reference to
the Brule. “The primeval forest overhangs the river on both
sides and the picture as nature originally painted it remains
intact. The rustic furniture and other handiwork of nature are
the same today as they were when the red man alone paddled his
canoe upon its waters”. “The public and the clubhouse people on
the Brule do not get on well together. The latter own a great
deal of the land on the river and their enjoyment would be
unalloyed if they could keep all other persons from fishing in the
waters of the Brule. They will not let a person erect a tent on
their lands.” The record of one party of four men staying at Joe
Lucius clubhouse was as follows : “Captain McDougall caught a
fine string and some of them were big fellows. G. L. Rice caught
74, McHugh and Monson each caught as many as their con-
O'Donnell — Fishing in the Brule River
27
sciences would permit of.” "Mr. A. W. Shaver caught 100 trout
and then quit when they were biting the best, remarking to his
guide: ‘Bill, this is too much like club fishing; guess I'll quit/”
The lumber interests started cutting in 1892 and had all of
the virgin timber cut by about 1909. During this period, when
the logging dams were in the river, the catch of speckled trout
continued to decline. By 1906 many complaints were being made
that something had to be done to save the trout. About 1905,
Henry Clay Pierce started to build his estate and one of the fea¬
tures was a large fish hatchery where he produced speckled
trout. "It is stated that in his ponds at the present time (1908)
there are enough trout to put the Brule back in the class of the
best streams in the entire country. They are of all kinds and
sizes.”
In 1906 an article was written on "The Boise Brule” in which
are given many statements in regard to the fishing.
"It is the real and ideal home of the trout. In the days
before logging dams were built it was filled with brook
trout. An ordinary fisherman might catch a hundred fish
a day with hook and line, old fishermen tell you. The
upper river is surrounded by innumerable springs which
form a natural home for trout. The logging dams have
created great havoc among the fish during the past few
years, as they interfere with the yearly migration of the
trout, these fish following the habits of the salmon. The
dams almost depleted the stream for the reason that there
was no fish way and the mature trout could run out but
could not return the next year. A few years ago rainbow
trout were planted in the river, and these have grown and
multiplied very rapidly. The fish do not migrate to and
from the lake as do the brook trout (the present stock of
rainbow' trout in the Brule River migrate to and from
Lake Superior) . To a certain extent this drawback of the
dams has been remedied, as most of the lumber is cut. It
has been proposed and in fact is being strongly urged by
a number of prominent people (notably Hon. C. D. O’¬
Brien and Mr. Weyerhouser) that the state of Wisconsin
take steps declaring the Brule River and its valley for a
mile on either side a state park forest and fishing pre¬
serve. This would give to the people of the state, and
country generally, one of the most beautiful resorts in the
northwest, wTould prevent for all time the building of
dams and cause the removal of present obstructions, and
bring back to its original conditions the fairest river of
the northwest, the Bois Brule.”
28 Wisconsin Academy of Sciences , Arts and Letters
In 1909, during the last part of July, the floods on the Brule
were reported as follows : “The rain Tuesday started the floods
which are reported to have destroyed some of Cedar Island.
Last night the river was more unruly than ever and the waters
were inundating the surrounding country. The loss to the Pierce
estate alone is estimated at many thousands of dollars and other
lodges and cottages along the shore have been wrecked by the
rioting river.”
Among the notables to visit the Brule was General Grant,
who came here in the 70’s on a fishing trip. Grover Cleveland
was the guest of Senator Vilas at his lodge on the Brule in the
80’s and Calvin Coolidge spent the summer of 1928 on the Brule
and was entertained by Henry Clay Pierce.
In 1936, with the use of WPA labor, a project of “stream im¬
provement” was started on the river. In that year a total of 232
structures, such as deflectors, bend covers and other “stream
improvement” devices, were installed in the stream. In addition
13 beaver dams were removed. In 1937, the work was continued
and 36 structures were placed in the river with 17 additional
structures being installed in 1938, plus 1,829 yards of dredging
in Big Lake and Lucius Lake. The cost of the “improvement”
work was approximately $40,000. In addition to the WPA pro¬
gram, a vast amount of work was done by the CCC, such as
installing structures, planting willows and cleaning out large
amounts of down trees and other materials in the river which
provide cover for trout. The particular stress at this time was
to convert the river into a comparatively “easy” canoe stream.
On January 12, 1938, the Conservation Commission issued!
an order, F-309, which prohibited all forms of fishing except
flyfishing on the Brule river between Stone's Bridge and Winne-
boujou. This order had been issued as a result of a petition con¬
taining 83 names of property owners. Of the signers, 19 were
from St. Paul, 9 from Minneapolis, 19 from Duluth, 4 from Lake
Forest, Illinois, 1 from Washington, D.C., 10 from Milwaukee,
1 from Superior, and 20 from Brule. The order, however, caused
such a storm of protest that on April 12, 1938, the Commission
issued order F-317 which rescinded order F-309.
For quite a number of years complaints have been made
almost yearly to the Conservation Department that something
should be done to improve the fishing. As a result of a com-
O'Donnell — Fishing in the Brule River
29
plaint made in December, 1941, that certain species of fish other
than trout be removed from the waters of the Brule River, a
check of the available information on the Brule River was made
at that time. It was found that the Conservation Department
possessed very little factual data on the physical, chemical, and
biological characteristics of the river; information which is
absolutely necessary in order to set up and execute an intelligent
and successful fish management program on any stream. It was
also found that although a number of cursory examinations had
been made of the liver, no management program had been or
even could have been made from these investigations. The usual
result was to increase the number of fish planted. In order to
determine the financial extent of the stocking, the plantings of
trout during the peiiod of 1937 through 1941 were checked. It
was found that a total of 616,850 brook trout, 150,175 brown
trout, and 464,850 rainbow trout had been planted. This amounts
to a grand total of 1,231,701 trout of all species which consisted
of 4,717 adults, 73,929 yearlings, 1,137,055 fingerlings and 16,000
fry. Based upon accumulative rearing costs a total of $34,247.67
had been expended in rearing the trout planted in the Brule
River over a five-year period. Thus a considerable expenditure
of funds was made with indeteiminate results and very limited
information was collected as a basis for a stream management
program.
As a result, it was recommended that a complete investiga¬
tion be made of the Brule River with the aim of establishing a
stream management program for the river. The Fisheries Foard
of the Conservation Department accepted these recommenda¬
tions and submitted a resolution to the Conservation Commis¬
sion requesting the creation .of a fund of $9,000 to permit a two-
year survey of the Brule River to determine the present existing
conditions and to then formulate a future fish management pro¬
gram.
The Conservation Commission acted upon the above resolu¬
tions at their July meeting, 1942. At that time they created a
fund of $9,000 to be used for a two-year study of the Brule
River. Also, to aid in the execution of this study, the Conserva¬
tion Commission asked the University of Wisconsin to assist in
the undertaking. As a result of the above actions a co-operative
agreement was completed in August, 1942, between the Wis-
30
Wisconsin Academy of Sciences , Arts and Letters
consin Conservation Commission and the University of Wiscon¬
sin for the detailed survey of the Brule River. The actual in¬
vestigation started on October 1, 1942, and will continue for a
period of two years, after which time, a tentative fish manage¬
ment program will be formulated for the Brule River based upon
the critical examination of the results obtained from the surveys.
Literature Cited
Andrus- Juneau, Isura
1941. The Brule-St. Croix Portage. Douglas County Historical Museum
Collections. Superior, Wisconsin.
Carver, Jonathan
1838. Travels in Wisconsin. Harper & Brothers.
Curot, Michel
1803. A Wisconsin fur- trader’s journal. Wisconsin Historical Collections,
20, 1911.
Doty, James Duane
1895. Expedition with Cass and Schoolcraft, 1820. Papers of James Duane
Doty. Wisconsin Historical Collections, 13.
Kellog, Louise Phelps
1928. The Historic Brule. The Wisconsin Archeologist, 8: 1.
Lucius, Jos. and Charles E. Brown
1941. The Blue Springs Indian Shrine. Trans. Wise. Acad. Sci. Arts
and Letters, April, 1941.
McManus, James H.
1920. The trails of Northern Wisconsin. The Wisconsin Magazine of His¬
tory, 4: 125-140.
Pickering, H. G.
1933. The Brule. The Anglers’ Club Bulletin, 12: 1, New York.
Schoolcraft. Henry Powe
1834. An exploratory trip through the St. Croix and Bumtwood (or
Broule) rivers in 1832. Harper & Brothers.
1851. Personal memoirs of a residence of thirty years with the Indian
tribes on the American frontiers. Lippincott.
St. John, John R.
1846. A true description of the Lake Superior country. New York.
Sweet, E. T.
1880. Geology of the Western Lake Superior District. Geology of Wis¬
consin, 3: 321-322.
Turner, Frederick J.
1889. The character and influence of the fur trade in Wisconsin. Proc.
36th Ann. Meet. State Hist. Soc. of Wisconsin-
Wilson, Leonard R.
1938. The postglacial history of vegetation in northwestern Wisconsin.
Rhodora, 40: No. 472.
The Superior Evening Telegram:
June 21, 1884; May 23, 1885; March 4, 1892; March 5, 1892; Oc¬
tober 14, 1893; October 5, 1894; April 11, 1895; April 27, 1895; Feb-
O'Donnell — Fishing in the Brule River 31
ruary 3, 1904; June 26, 1905; May 5, 1906; October 22, 1908; July 22,
1809; July 15, 1910; September 4, 1911; July 15, 1912; August 7,
1915; November 27, 1915; June 26, 1928; March 18, 1931; January 7,
1938; January 21, 1938; April 20, 1938; May 2, 1938; July 5, 1938;
October 13, 1938; October 24, 1939; June 11, 1940; February 2, 1941;
May 14, 1941.
The Wisconsin State Journal:
January 7, 1938; February 4, 1938; February 11, 1938.
' 1 ' \ ' - ,
'
- '
.
.
‘ !•' !
N ' V
,
'
V'L.
VEGETATION OF THE BRULE BASIN,
PAST AND PRESENT
Brule River Survey: Paper No. 4
Norman C. Fassett
The Brule River flows northward in eastern Douglas County,
Wisconsin, to Lake Superior (Map 1). It is notable to geologists
in that it occupies the valley carved by the outlet of the Glacial
Lake Duluth, which was in the western end of what is now Lake
Superior, during the recession of the Superior lobe of Substage
4 of Wisconsin glaciation. It has long been notable to sportsmen
as a trout stream ; indeed, this study was initiated for the pur¬
pose of determining whether there have been changes in the
vegetation of the drainage basin which might be responsible for
changes in the environment of the fish.
Map 2 was derived from a study of the notes of the govern¬
ment surveyors who laid out the section lines in the region in
1852-56. Map 3 was derived largely from the survey in 1932 by
the Wisconsin Land Economic Inventory, somewhat modified by
notes of the Wisconsin Geological Survey in 1925 and by per¬
sonal observation in 1942-43. Details of the methods of deriving
these maps will be discussed later.
The Brule Basin may be conveniently divided into four gen¬
eral areas, (1) the gorge of the upper Brule, shown by the brown
band along the river on Maps 2 and 3, (2) the sand barrens,
shown mainly by the stippled red on both sides of the upper
Brule on Map 2, (3) the valley of Nebagamon Creek, the largest
tributary, entering the Brule in T.47, R.10W., and (4) the lower
Brule basin, embracing essentially the area in solid pink and
solid orange on the northern third of Map 2.
The Bog
The upper Brule is remarkable in that it flows northeastward
in the ancient channel of a much larger stream, the outlet of
Lake Duluth (which occupied what is now the west end of Lake
Superior) in early post-glacial times, and floored southwestward
S3
84 Wisconsin Academy of Sciences , Arts and Letters
to what is now the St. Croix River and eventually to the Missis¬
sippi. The route of this outlet, south and southwest through
what is now the Brule, past Solon Springs and down the St.
Croix, may be easily traced on Map 1. This channel was cut
through sand, and is now occupied by a continuous bog (brown
on both maps). On every section line crossing the river in this
region the surveyors of 1852-56 recorded the fact that they
entered a bog, covered largely with White Cedar, Tamarack, and
Black Spruce. Their descriptions are quite consistent with that
of Owen,1 who wrote: “The whole country has a very singular
aspect, with lakes [several lakes, represented as one continuous
lake in the northern part of T.46N., R.10W. on Maps 2 and 3]
of still water, connected by short and swift rapids, that meander
through a dense growth of cedar and tamarack. . . . After navi¬
gating four lakes [Owen is traveling up-stream] . . . the Brule
meanders through a series of cedar swamps, separating into
several channels, the main one being sixty or seventy yards
wide. . . . The river now very soon contracts its dimensions to a
mere creek, just wide enough to float a canoe between the bushes
that overhang its banks.” In 1880, Sweet2 wrote : “The head of
the Brule is less than two miles from the Upper St. Croix lake
[the head of the St. Croix River, which still flows to the Missis¬
sippi]. Several small spring branches unite with the main chan¬
nel in the northern part of T.45N., R.11W., and the exceedingly
sluggish stream winds through dense cedar, tamarac and alder
swamps, for a distance of eight or ten miles.”
These descriptions, some nearly a century old, are just as
applicable today. Nearly all of the long narrow bog shown in
brown on Map 1 is duplicated on Map 3. Plates 1-3 show various
places along this bog as they now appear. In a few places
(Plate 4) the trees have been cut and the land probably burned
over; here the bog is quite spoiled and has gone to grass or
sedge-meadow.
The Barrens
The Barrens, developed chiefly on an outwash sand plain,
are shown on the maps by red stippled areas, and originally
1 David Dale Owen, Report of a geological reconnaissance of the Chippewa Land District.
Senate Executive Document 57; 58-61. 1848.
2 E. T. Sweet. Geology of the western Lake Superior district. Geology of Wisconsin, 3:321*322.
1S80.
Fas sett — V eg elation of the Brule River Basin 35
(Map 2) extended for several miles on each side of the upper
Brule. The appearance of this region three-quarters of a century
ago can be best portrayed by a few verbatim excerpts from the
notes of the surveyors.
On the line between T.45 and 46N., R.10W., in May, 1855.
Travelling west between Sections 3 and 34:
“40 :00* 3 set % section Post
Black Pine 5 N 28 W 45 links4
Black Pine 5 S 58 W 32 links
“80:00 Set corner to Sections 3, 4, 33 and 34
Black Pine 5 N 54 W 28 links
Black Pine 5 N 80 E 28 links
Black Pine 5 S 5 E 51 links
Elack Pine 5 S 20 W 61 links
“Surface rolling.
“Pine barrens.”
A little calculation will show that these 5-inch Jack Pines,
presumably the largest trees at that location, were spaced ap¬
proximately 80 feet apart.
On the same line, west between Sections 5 and 32 :
“40:00 Set % Section Post
Dead Black Pine 8 S 49 W 40 links
Dead Black Pine 9 N 28 E 50 links
“80:00 Set corner to Sections 5, 6, 31 and 32
Dead Black Pine 10 N 45 W 53 links
Dead Black Pine 10 N 66 E 59 links
Dead Black Pine 10 S 50 E 31 links
Dead Black Pine 10 S 25 W 36 links
Black Pine 5 N 28 W 45 links
“Black Pine Brush from 4 to 8 feet high as thick as it can
stand. No green timber in sight.”
After surveying a township (36 square miles) each sur¬
veyor wrote a brief description of it. The one for T.46N., R.9W.,
written in September, 1856, is characteristic of the regions
shown as stippled red on Maps 2 and 3 : “This is a Township of
barrens that is almost worthless for agricultural purposes, or
anything else, as there is but very little Timber in it, and that is
scrubby Black Pine; and there is hardly a drop of water in the
Township, in fact notv, except [for?] small ponds in the South
“These figures indicate chains from the section comer at which the surveyor commenced;
there are eighty chains to a mile.
4 Black Pine is . Jack Pine. Pinus Banksiana. The “5” indicates diameter at breast height,
in inches. This tree was 45 links from the corner post, and the direction was 28 degrees west -of
north; a link is 7.92 inches.
36 Wisconsin Academy of Sciences , Arts and Letters
end of it [outside the Brule basin] , the Prairie that I have note#
on the West side; can hardly be called a Prairie, as no very great
time has elapsed since it was covered with small Pine which has
been blown down, and burned up, remnants of which still lie on
the ground.” (Some of these surveyors may have been weak in
the rules of punctuation, but they could write a vivid descrip¬
tion.)
In the township just described there were occasionally no
witness trees at all ; for example, at the quarter-section between
sections 18 and 19, the surveyor “Set quarter Section post in a
Mound of earth and sod, drove charred stick 10 inches long.”
Not even a stick of uncharred wood was to be found 1
The monotony of small Jack Pines was occasionally broken
by a few scattered large Norway Pines ( Finns resinosa, called
“Yellow Pine” by many surveyors). In T.46N., R.10W., going
north between Sections 22 and 23, in August, 1854, the record
runs:
“40:00 Set quarter Section Post
Black Pine 6 N 34 E 22 links
Black Pine 6 S 43 W 6 links
“80:00 Set post corner to Sections 14, 15, 22 and 23
Black Pine 10 N 45 W 1.40 links
Yellow Pine 20 S 40 E 180 links
“Surface rolling. Soil 3d rate
“Timber Pine — brush.”
In T.45N., R.10W., at the quarter-section post between sec¬
tions 6 and 7, the record is: “Yellow Pine 20 S 35 E 1080 links.
No other near.” The nearest tree at this point was therefore
more than 700 feet away, a large Norway Pine towering over
the brush.
Description of T.46N., R.10W. as of 1856: “This is one of
those barren Townships that is almost worthless for agricul¬
tural purposes. The Surface is rolling excepting that portion
adjoining the Brula, which is very broken; the Brula River flows
through a valley that is 150 or 200 feet below the general level
of the country ; on the east side of the River the Bluffs are steep,
but on the West side the land rises gradually from the River
bottom, so that the top of the Bluff cannot well be defined ; the
River bottom is one continuous Cedar Swamp that is miry and
unfit for cultivation. The timber on the entire Township is
worthless.”
Fassett— Vegetation of the Brule River Basin 87
On Map 4 the figures indicate the diameter at breast height,
m inches, of Jack Pines used as witness trees. A dot on a section
line indicates that the species was recorded as present, but not
used as witness trees. The significant thing about these trees as
recorded on the map is the uniformity of size in many regions.
There is a large area, for example, in T.45N., R.10W., where
nearly all the trees are five inches in diameter. In southeastern
T.46N., R.10W. there is another area of uniformity, the trees
here being six inches. These large areas of trees of uniform size,
and therefore uniform age, are without doubt due to the ability
of this species to repopulate an area after a fire. Near the
Brule River, and along the northwestern border of the range of
the tree in this area, fires were not quite so frequent and wide¬
spread, and the Jack Pines were less uniform and reached a
larger size.
Next to Jack Pine, the most abundant trees on the Barrens
were Oaks. Occasionally an Oak reached a diameter of ten
inches, but most of them were described as Oak Brush.
The barrens of 90 years ago, then, were a region of frequent
fires, covered with small Jack Pine of a uniform size in each
area, the size dependent upon the elapsed time since the last
severe fire; occasionally a few large scattered Norway Pines
were present. Oak trees and Oak Brush often accompanied and
sometimes replaced the Pines.
The barrens as they appeared in 1942 are shown in Plates 5
to 7. They are frequently burned and nearly treeless; Plate 7
Is in the area of the great fire of 1936. Often they are covered
with small Jack Pine of a uniform size in each area (Plate 5).
Occasionally a few large scattered Norway Pines are present
(Plate 6). Oak trees and Oak Brush often accompany and some¬
times replace the Pines.
The Valley of Nebagamon Creek
The surveyor’s description of T.46N., R.11W. is short but
brings out a significant point. “This Township is heavily tim¬
bered with Oak Maple Sugar,3 Aspen and Pine: and a dense
undergrowth of Hazel and Aspen. The surface is rolling: and
covered with rock: = trap rock. The soil is of the poorest
quality. A great deal of the timber is down, patches of windfall
*The “Maple” of the surveyors is Red Maple; Sugar Maple is almost invariably called
“Sugar.”
38 Wisconsin Academy of Sciences , Arts and Letters
thickly scattered over the entire Township.” This description
indicates diversity in forest cover, for Sugar Maple is a climax
tree in this region, while Hazel and Aspen are usually the result
of fairly recent burning. An expression of this diversity, as well
as some indication of the reason, may be seen on Map 2. The
valley of the Nebagamon occupies the western part of T.47N.,
R.10W., the southeastern part of T.47N., R.11W., and the north¬
western half of T.46N., R.11W. This area is dissected by num¬
berless bogs of various sizes (in brown on Map 2) and lakes.
Under these conditions, fires, which seem to have been the major
factor in setting back the ecological succession, would have been
much less widespread than on the broad flat sandy barrens.
Much of the region suffered from fire and was largely in Aspen
(stippled orange on Map 2). But where somewhat protected
from the spread of fires, in the neighborhood of lakes and bogs,
mixed pine-hardwoods developed (orange on Map 2), or the
succession even went to climax forest (yellow on Map 2).
Most of the soil in the valley of the Nebagamon is loam, but
along its northwestern border, and thence running northeast¬
ward across the Brule valley, is the Copper Range, a ridge of
trap rock (Map 11). Conditions on the Copper Range appear to
have favored the development of climax forest; most of this
forest was just outside the Brule Basin paralleling its north¬
western border, but the strip of yellow northwest of the large
bog in T.47N., R.11W. is the edge of this forest. Just northwest
of this strip of yellow on Map 2, about a mile outside the Brule
Basin, is the present-day town of Maple6 (Map 12).
Maps 9 and 10 show the locations of trees .of five species,
taken as indicators of climax forest.
When compared with Map 2, Map 3 shows considerable
change in the land cover of this area. Much of the land is
cleared, particularly in the vicinity of the larger lakes. Con¬
siderable portions of the bogs seem to have had their flora
altered, so that some parts are now better classed as Black Ash,
Red Maple and Elm (olive-green on Map 3) or Tagalder, Willow
and Dogwood (stippled olive-green on Map 3) than as Tam¬
arack. This is however a difficult point to judge, for all of these
species were doubtless present on the bogs when the surveyors
traversed them, and all are now present. Close study of the
9 “Maple,” in this case, is without doubt Sugar Maple.
Fassett— Vegetation of the Brule River Basin 39
surveyors* notes, and then of the Land Economic Inventory maps
and of the areas themselves, indicates that there have been in
some areas changes in the proportions of each species, from a
predominance of bog conifers to a predominance of broad-leaved
species. But certainly Maps 2 and 3 cannot be interpreted liter¬
ally to the extent of stating that any particular acre of ground
has undergone a specified qualitative or quantitative change.
Comparison of bog areas on these maps also shows that much
of what the surveyors indicated as bog is now covered with
aspen.
Besides the possible destruction of much of the bog area,
another result of the occupation of this region for about a cen¬
tury has been the degradation of the forests, so that most of
what was mixed pine-hardwoods or climax forest on Map 2 is
now Aspen scrub (Plate 8). Close inspection of Map 3 will show
a few small remaining stands of White Pine (Plate 9), mixed
forest, and even Sugar Maple.
The Lower Brule Basin
The soil in the lower Brule Basin is red clay, deposited under
the waters of Glacial Lakes Duluth and Algonquin. The areas of
red clay are shown approximately on Map 11. This clay has
great water-holding capacity ; it dried out much less easily than
did the sand and the loam, and so was less subject to fires. This
region was therefore the most heavily wooded of all the Brule
Basin, and here grew the largest individuals of White Pine (Map
5), Fir (Map 7), and Aspen (Map 8). 7
In September, 1852, T.49N., R.10W. was described as fol¬
lows:
“This township has a clay soil. The surface is gen¬
erally level back from the streams. The Streams except
Brule River fail during the dry season but during the
spring and fore part of the Summer offered plenty of
water, running as they do through a clay formation. The
valleys are narrow gullys or ravines.
“It is well timbered with White Pine in every part and
Brule River offers every facility for a lumbering business.
This stream rises in the small lakes south of the Summit ;
through which it breaks and discharges its self into the
Lake after [falling?] over 100 distinct rapids in its de-
7 This probably includes both the Trembling Aspen and the Large-toothed Aspen. Perhaps Hhe
larger Aspens of the clay region were mostly the latter species.
40 Wisconsm Academy of Sciences, Arts and Letters
scent. Every bend has its rapids through this township
until it [flows?] into Section 10 [at the mouth of the
stream] where the water becomes sluggish and deep.
“During the months of April and May the Indians and
Trappers carry on a successful fishing business along the
lake shore. Trout Whitefish and Siskowet being the prin¬
cipal kinds packed for the market.
“The waters of the small streams are so strongly
chalybeate that the leaves turn them black in the fallp?
The witness trees were, in order of frequency: White Pine*
up to 30 inches and averaging 18 inches; Spruce (doubtless
White Spruce), up to 16 inches and averaging 11 inches; White
Birch, up to 19 inches and averaging 11 inches; Black Ash up to
16 inches; White Cedar up to 14 inches; Yellow Pine up to 20
inches; Fir up to 12 inches; Tamarack up to 16 inches (appar¬
ently growing larger on the clay than in the bogs) ; Red Maple
up to 12 inches; Aspen up to 22 inches; and Black Oak. The
trees most frequently mentioned in the summaries of each mile*
were, in order, Spruce, Fir, Birch, Pine, Aspen, White Cedar*
Tamarack, Ash and Red Maple, while the undergrowth was
almost always described as Alder, Hazel and Green Ozier, some¬
times Maple (probably the Mountain Maple, Acer spicatum ).
This mixture is shown on Map 2 as Spruce-Fir. Woods of
this type were seen in 1942-43 only on the high ground near the
abandoned house on the west side of the river near its mouth
(Plate 10). Elsewhere the forest has been destroyed by lumber¬
ing, fires, and agriculture, so that much of the area is now
cleared land (Plates 11 and 13) and the rest has a scrubby
growth of Alders, Willow and Red-osier Dogwood (stippled
olive-green on Map 3), grading to Aspen and small Firs on the
higher ground (stippled pink on Map 3; Plate 12). A few areas
are shown on Map 3 as mixed Pine-hardwood (orange) and as
Aspen (stippled orange), but actually these four types grade
into each other and the boundaries must not be interpreted to©
strictly.
The description of T.48N., R.10W., written in August, 1852.
reads as follows :
“This Township is well watered and well timbered.
The Streams get low during the dry season but do not dry
up entirely. The surface is gently rolling and hilly. The
soil clay and sand, wet, adapted to the raising of Grass.
The timber is large and valuable.
Fassett — Vegetation of the Brule River Basin 41
“Bois Brule River runs through the center of the
township, is a rapid durable stream affording every fa¬
cility for a Lumbering business. Mines are reported to
have been worked in this Township on Section 18 or 19
but were not found by me. On Section 23 overlooking the
river the Amygdaloid Trap Rock is Magnetic and re¬
sembles cast iron in lustre when broken. Traces of copper
were found on Section 27.
“The local attraction of the needle was so great that
the plain compass could not be used in the vicinity of hill
extending across the Township.”
The Copper Range (Map 11) was well forested; between
Sections 22 and 27 the summary reads “Black Oak, Sugar, White
Fine, Yellow Birch, Lind [— Basswood], Elm, Aspen, White
Cedar, Fir, Spruce and Tamarac.” The Sugar Maple, Basswood
and Yellow Birch may be taken as indicators of climax forest.
This hill (Plate 13) still shows the species which were origi¬
nally listed; but the woods have been cut and burned, and the
hardwoods are sprouting from the stumps (Plates 15 and 16).
As compared with the uniformity of the township directly
to the north, this showed a smaller number of species on each
mile, but greater variation between miles. Pines were general
throughout the township, but where they were accompanied by
Spruce and Fir the land has been shown on Map 2 as “Spruce-Fir
forest,” and where they were mixed with Oaks, Linden, Maple,
etc. “mixed hardwood” has been the designation. Now, of course,
the big pines are cut, and their charred stumps are in a dense
growth of Aspen (Plate 16). A few good stands of forest re¬
main along the River (Plate 14).
An area of about 8 square miles in the northwestern part of
T.47N., R.10W. and the southwestern part of T.48N., R.10W. is
shown as Alder-Dogwood- Willow on the recent map and as mixed
hardwoods on the old map. This is a poorly drained area which
seems to have a very mixed vegetation. The surveyors recorded
Tamarack in every mile traversed (even excluding those re¬
ported in swamps), White Pine in every mile, the largest being
20 and 26 inches, Aspen, Birch, Spruce, Fir and White Cedar
almost always, Maple and Yellow Pine often, and occasionally
Yellow Birch, Black Ash, Sugar Maple and Elm. The under¬
growth was usually described as Elder, Hazel, Green Ozier and
Maple. Excluding the larger trees, this is much as the area is
(today ; it is mostly covered with swamp shrubs, with a few trees
42
Wisconsin Academy of Sciences , Arts and Letters
©n the better-drained locations. Geologists Emrich and Schafer,
in 1925, recorded T.47N., R.10W., between 7 and 8, as Alder,
Maple, Ash, Birch, Cedar and Spruce. The Land Economic Sur¬
vey, in 1933, recorded it as recently burned. The original vegeta¬
tion of this area seems to have been much like that in T.49N.,
R.10W. shown as Spruce-Fir on the map, except that here the
proportions of these two species are much lower.
Sources for Data
The exterior lines, which are those forming the boundaries
of the township, were surveyed by the following deputy survey¬
ors, in the following years :
These surveys were conducted from June to November; each
township took a week or ten days. For each section corner and
quarter-section (one in the middle of each mile) two witness
trees were recorded ; for section corners on exterior lines there
were four witness trees. At the end of each mile the principal
trees seen along that mile were listed. For each township there
was a general summary.
Fassett — Vegetation of the Brule River Basin 4S
These records were studied by Dr. John T. Curtis and the
writer in the fall of 1942 and a map of the vegetation as of
1852-56 was drawn. When Dr. Curtis was called to conduct some
work in Haiti the writer continued alone, later revising this
map. In some cases, determining the vegetation of a section line
has been easy. If only small Jack Pine of uniform diameter is
listed, it is pine barrens, and if only small Aspen is listed, it is
as obviously Aspen thicket. Bogs are easy, particularly since
the surveyors made up maps showing the outlines of the bogs.
It must be noted, however, on Map 2, that small bogs are shown
only on section lines, since those in the interior of the sections
were not seen by the surveyors.
Some sections have been very difficult to classify, and a few
examples will be given to show the method of interpreting the
meagre data.
T.47N., R.10W., west between sections 28 & 33. At the quar¬
ter-section post were recorded an Aspen 8 inches D.B.H., 35 feet
from the post, and a Black Pine 6 inches D.B.H., 40 feet from
the post. The summary of the mile was: Timber Pine Birch
Aspen and Lind. Undergrowth Alder & Hazel, woods very thick.
Seldom can you see more than 2 chains.” Here the Basswood
(“Lind”) would suggest that the forest was developing toward
dimax, but it is listed last and was probably the least abundant ;
also, Basswood is so rare in the region that any occurrance would
be noted. The witness trees are Jack Pine and Aspen, both some
distance from the post, so the trees were not very closely spaced.
Visibility is low due to density of growth, but this dense under¬
growth is Alder and Hazel. The picture develops, therefore, as
a sparse growth of medium-sized but fast-growing trees, prob¬
ably not over 20 years old, with a dense scrubby undergrowth.
This is recorded on Map 2 as Aspen scrub (stippled orange).
T.47N., R.10W., north between sections 1 & 12. At the quar¬
ter-section post were recorded a White Cedar 10 inches D.B.H.
and a Yellow Birch 9 inches D.B.H. The summary was : “Spruce
Yellow Birch Tamarack White Pine Aspen & Black Oak. Under¬
growth Birch & Fir.” The southern half of this section line was
recorded as bog, which accounts for the Tamarack and the White
Cedar; the latter was south of the quarter-section post and so
located in the bog. The higher ground had Yellow Birch which
is ordinarily taken as indicating climax forest, but here it was
44 Wisconsin Academy of Sciences , Arts and Letters
mixed, not with Sugar Maple, but with Pine, Spruce, Oak and
Aspen. This section line is therefore recorded on Map 2 as
Mixed Pine and Hardwoods (orange).
These examples are given to show that there may be some
question regarding the type of vegetation on any particular mile.
However, it is the opinion of the writer that the generalizations
drawn from these records are reliable; while Map 2 may not
represent accurately each individual mile, it is correct in show¬
ing that the region southeast of the upper Brule was in Barrens,
and that the regions about Lakes Nebagamon and Minnesuing
were a mixture of bog, Aspen thicket, mixed forest, and Maple
forest.
Map 3 was made up primarily from the Land Economic In¬
ventory maps of Douglas County, published in 1933, and of Bay-
field County, published in 1928. The classification of land cover
used on these maps differs in some respects from that used on
Map 3, so that there was in some cases a question of interpreta¬
tion. A preliminary map made up from the Inventory maps was
used in the field, and checked with conditions as observed in 1942
and 1943 by the writer, with the help and advice of Dr. John W.
Thomson and Mr. E. F. Bean. While not assuming to make cor¬
rections on the Inventory maps, the writer has taken the privi¬
lege of making his own interpretation both of the Inventory
maps and of the observed land cover. In many cases changes
were necessary due to actual changes in cover since the Inven¬
tory surveys. Some of this area was surveyed by a party of the
Wisconsin Geological Survey, and notes on the vegetation made
by Geologists D. G. Emrich and Sidney Schafer. Again, their
classification of land cover was different from those used by the
Inventory survey and by the writer, but their notes have proved
useful in several areas.
Maps 4-10, showing the ranges of individual species of trees,
are compiled entirely from the surveyors’ reports. The figures
represent D.B.H., and each is placed near its appropriate section
or quarter-section corner, in the direction, but not at the dis¬
tance from the corner, in which the tree was recorded. A dot on
a section line means that the species was mentioned in the sum¬
mary of that mile.
The data concerning soils on Map 11 are from the General
Soil Map of Wisconsin by A. R. Whitson and others, published
Fassett— -Vegetation of the Brule River Basin 45
in 1926 by the Wisconsin Geological and Natural History Sur¬
vey. Since the soils boundaries on this map were very general,
and are moreover transferred to a larger scale by their use on
Map 11, they must not be regarded as accurate within the Brule
Basin, but rather to indicate broadly the areas of different soils.
The rock outcrops on Map 11 are from the Land Economic Sur¬
vey, and the location, but not necessarily the exact boundaries,
of the Copper Range are sketched in from field observation.
Vegetation and Water Flow
While the Brule Bog remains undamaged, the upper Brule
River will continue to be as it is now ; cutting the trees or burn¬
ing the bog would reduce the Brule River to a warm-water
stream, probably to one devoid of trout. In the Barrens, water
seeps into the sand and enters the Brule River as springs, in
spite of the fact that the vegetation of the barrens has been
burned since time immemorial; future burning will therefore
do no damage. Much of the Nebagamon River Basin is now less
heavily forested than it was in the past; partial restoration of
the forests should be effected. The area of Red Clay along Lake
Superior presents a complex problem: the forest has been very
largely destroyed and the water-holding capacity of the upper
soil levels doubtless reduced, but erosion on farm lands and road¬
sides, and the slumping of clay banks, probably present the most
serious problems.
Summary
The vegetation of the drainage basin of the Brule River,
which enters Lake Superior in northwestern Wisconsin, has been
determined, as of 1852-56, by a study of witness trees and field
notes recorded by the government surveyors of those dates, and
as of 1932-48 by study of the Land Economic Survey maps of
1933 and by direct observations in the region. The bog, about a
mile wide and ten miles long, which borders the upper Brule is in
nearly its original condition, except for the removal of scattered
large pines and the complete cutting and burning of a few small
portions. The sandy Barrens, mostly southeast but also to some
extent on the northwestern side of the upper Brule, is frequently
burned over, with a usually sparse ground cover of small Jack
Pines and scrub oaks, just as it was a century ago. The valley
of the principal tributary, Nebagamon Creek, originally had a
46 Wisconsin Academy of Sciences , Arts and Letters
land cover varying from pine barrens and Aspen scrub to mixed
pine and hardwoods and Maple forest. This was because it was
so dissected by lakes and bogs that fires were local, rather than
widespread as in the Barrens. Much of this area is now cleared,
the patches of maple and of pine are much reduced, and aspen
scrub has largely replaced the better types of forest. The Copper
Range, a ridge of trap rock crossing the Brule valley parallel to
and about nine miles south of the Lake Superior shore, origi¬
nally had a good growth of Maple- Yellow Birch forest, now early
destroyed and represented by local areas of maple coppice. The
red clay, bordering Lake Superior for about ten miles in this
region, was covered with dense forest of White Pine, Spruce,
Fir, White Birch, Black Ash, White Cedar, Yellow Pine, Aspen,
etc., with an undergrowth of Alder, Hazel, Red Maple, Osier and
Willow. The cutting, burning and pasturing has left most of this
area with a shrubby growth of Alder, Hazel, Osier, and Willow,
with some patches of Aspen and little Fir trees.
47
Fassett— Vegetation of the Brule River Basin
Map 1. From the House of Representatives Document No. 227, 72nd Congress, first session.
48 Wisconsin Academy of Sciences, Arts and Letters
R.IIW.
mow
1852-56
□ Mapfe —Yellow Birch
0 Maple Coppice
H Pine -Hardwood
M Aspen
B Pine Forest
H Pine Barrens
0 Spruce-Fir Forest
m Small Fir and Aspen
SS Lowland Hardwoods
§1 Willow, Alder, etc.
HI Bog Conifers
H Cleared
SB Marsh
T.49N.
T.48N.
T.46N.
T.45N.
R.IIW. R.IOW.
MAP 2
1932-43
T.45N.
T.46N.
□ Maple -Yellow Birch
H Maple Coppice
■ Pine - Hardwoods
11 Aspen
Pine Forest
H Pine Barrens
0 Spruce- Fir Forest
El Small Fir and Aspen
■ Lowland Hardwoods
■ Willow, Alder, etc-
■ Bog Conifers
11 Gleared
S3 Marsh
T.48N.
T.49N.
RHW. R.IOW.
MAP 3
Fassett — Vegetation of the Brule River Basin 49
R.IIW.
R.IOW.
§0 Wisconsin Academy of Sciences, Arts and Letters
RJIW.
Fassett—V eg elation of the Brule River Basil} 51
RJIW
R.IOW,
52 Wisconsin Academy of Sciences , Arts and Letters
R.IIW.
R.10W
Fassett — Vegetation of the Brule River Basin 53
R.IIW.
R.iOW
54 Wisconsin Academy of Sciences , Arts and Letters
Map 10-
CLIMAX
FOREST SPECIES
1852 - 56
L= Linden
Y s Yellow Birch
H = Hemlock
I = ironwood
T.49N
T.48N.
T.47N.
T.46N
T.45N
R It W
R.IOW
Fassett — Vegetation of the Brule River Basin 55
R.IIW.
R.iovv.
Wisconsin Academy of Sciences , Arts and Letters
TOWNS HIGHWAYS and BRIDGES LAKES
Mapl2.
Plate 1. Looking eastward across Brule Bog. Sec. 3, T.45N.,
R.11W. Photograph by Dr. J. W. Thomson.
Plate 2. The Brule Bog near Cedar Island. Sec. 21, T.46N., R.10W.
Plate 3. The Brule Bog near Stones Bridge. Sec. 30, T.46N., R.10W.
Plate 4. The Brule Bog at Highway P. Sec. 8, T.45N., R.11W.
Ml*
Plate 6. The Barrens. Sec. 32, T.48N., R.10W.
Plate 7. The Barrens. Sec. 35, T.46N.. R.10W.
Plate 8. Aspen scrub. Sec. 5, T.45N., R.11W.
Plate 10. Fir forest at the mouth of the Brule River. Sec. 10, T.49N., R.10W.
Plate 11. On the red clay, looking north. Sec. 23 and 24. T.48N., R.10W.
Plate 13. Cleared land on the red clay, looking southward to the Copper
Range. Sec. 15, T.48N., R.10W.
Plate 14. Fir, Pine, Birch, etc., at N. P. Johnson Bridge. Sec. 15, T.48N.
R.10W.
A SURVEY OF THE LARGER AQUATIC PLANTS AND
BANK FLORA OF THE BRULE RIVER
Bride River Survey: Paper No. 5
John W. Thomson, Jr.
This report is a result of a reconnaissance survey of the Brule
River from the headwaters to the mouth during 1943. Two full
sets of specimens substantiating the observations were collected.
One set is deposited in the Herbarium of the University of Wis¬
consin; the second set is in the Herbarium at Superior State
Teachers College. These specimens are designated by special
labels. No attempt was made at this time to obtain quantitative
data other than general observations on the abundance of the
aquatics. These data are expected to be obtained during the sum¬
mer of 1944.
Funds making possible the field work were supplied by the
Wisconsin Conservation Commission from funds allotted to the
Brule River Survey in cooperation with the University of Wis¬
consin. Grateful acknowledgement is made to Dr. N. C. Fassett
of the Department of Botany of the University of Wisconsin and
to Mr. J. R. Jacobson of Superior, Wisconsin for assistance dur¬
ing the project.
Major Divisions of the Stream
The Brule River may be divided into three major ecological
regions. The upper section extending downstream to the mouth
of Nebagamon Creek is dominated by the headwaters coniferous
swamp. It is a comparatively unspoiled section of the stream.
The lower section of this major region is divided into the upper
rapids or Dalles and the “lakes.” In this section is the greatest
abundance and variety of species of higher aquatic plants. The
middle section of the Brule, from the mouth of Nebagamon
Creek to the beginning of the rapids above Co op Park is a slug¬
gish, meandering stream flowing through bottomlands with large
hardwood trees, mainly elm and ash. Comparatively few aquat¬
ics are found in this section. The lower course of the stream,
57
58 W'isconsin Academy of Sciences , Arts and Letters
from the beginning of the rapids to the mouth, is a series of short
rapids and falls alternating with pools of quieter water. Except
at the mouth, the higher aquatic plants are extremely rare in
this lower section. The alga, Cladophoraf is the most abundant
macroscopic plant in the lower stream. The dominant bank
plants throughout the course of the river are the hoary or tag
alder and the red-osier dogwood. Other associations of plants
approach the river and contribute their effects upon it. These
associations are discussed in the appropriate stream sections.
The Upper Brule
If appears that the greatest factor in the maintenance of the
river as a suitable habitat for trout is the coniferous forest
swamp which occupies the upper valley. The numerous springs
in this region, and the large swampy area with an abundance of
absorbent humus make this stream unusual among most streams
in this area of northern Wisconsin and are good combinations
for maintaining a very even flow of water.
The Coniferous Swamp Association ( Thuja Association)
The white cedar, Thuja occidentalisf or Thuja association of
F. C. Gates is the dominant one of the upper valley. White cedar
and black spruce, Picea mariana , are the dominant trees. Tam¬
arack, Larix laricina, and balsam, Abies balsamea , are common
subdominants. Occasional deciduous trees occur. These are
mainly white birch, Betula papyri! era; black ash, Fraxinus
nigra ; and mountain ash, Sorbus americana. Where the associa¬
tion extends along the river, the same shrubs characteristic of
the alder swamp association occur in addition: honeysuckles,
Lonicera oblongifolia, L. caerulea var. villosa, L. canadensis ;
mountain holly, Nemopanthus mucronata ; mountain maple, Acer
spicatum ; and leather leaf, Chamaedaphne calyculata. The shade
of the dominants is not so unbroken but to allow a large number
of secondary species characteristic of the association to thrive.
They include: crested shield fern, Dryopteris cristata; rattle¬
snake fern, Botrychium virginianum; club mosses, Lycopodium
lucidulum and L. annotinum; yew, Taxus canadensis; cotton
grass, Eriophorum viridi-carinatum; sedges, Car ex laxiflora, C.
tenelia , C. trisperma , C. intumescens var. Fernaldii; china-
berry, Clintonia borealis ; three-leaved Solomon's seal, Smilacina
trifolia; blunt-leaf orchid, Habenaria obtusata; leafy orchid, Ha-
Thomson — Aquatic Plants and Flora of the Brule River 59
benaria dilatata var. media ; dwarf rattlesnake plantain. Good-
yera repens var. ophioides ; goldthread, Coptis trifolia ; bishop's
cap, Mitella nuda ; strawberry, Fragaria vesca ; fringed polygala,
Poly gala pauciflora ; enchanters nightshade, Circaea alpina ; one-
Howered pyrola, Moneses uniflora ; shinleaf, pyrola chlorantka
and P. secunda var. ohtusata ; snowberry, Chiogenes hispidula;
ibedstraw, Galium triflorum ; twinflower, Linnaea borealis var.
ameHcana ; bog goldenrod, Solidago uliginosa ; and aster, Aster
puniceus .
A thick mat of mosses principally composed of species of
Sphagnum , Thuidium , Brachythecium, Anomodon , Mnium , and
Dicranum carpets the ground and fallen logs. Lichens are nu¬
merous, including Cladonia rangiferina (classified in the narrow
sense) as the most abundant. Luxuriant thalli of Peltigera
aphthosa, P . horizontal is, P. polydactylaf and P. canina are abun¬
dant. Cladoniae are frequent. Cladonia cenotea , C . gracilis , C.
Morophaea , C. crispata , C. cristatella and C . nemoxyna are per¬
haps those most frequently seen. In open spaces where wind¬
falls expose the area to increased sunshine, labrador tea, Ledum
groenlandicum ; cranberry, Vaccinium oxy coccus; fireweed, Epi-
lobium angusti folium ; crested fern, Dryopteris cristata ; bunch-
berry, Comus canadensis ; and sundew, Drosera rotundifolia are
typical.
Bog acids which hinder decay and the coldness of the water-
soaked organic soil below the surface account for the accumula¬
tion of material in the valley. If this material is exposed to heat
and drying, the organic matter oxidizes, runs off via the stream,
and the soil disappears. Mr. J. R. Jacobson of Superior, Wis¬
consin, suggests that this may be occurring slowly due to the
©verbr.owsing of the white cedar association by deer with con¬
sequent more rapid evaporation from the soil. This hypothesis
seems reasonable and should be checked carefully in the field.
Forest removal, through fencepost and pulpwood cutting, will of
course vastly accelerate the destruction. Unfortunately certain
areas within this coniferous swamp (near Highway P crossing
in T.45N., R.11W., S.9,4) are being cut for pulpwood. Conse¬
quently the cut-over areas are drying out and the humus is de¬
teriorating. The destruction of the swamp by such a process will
lead to a lessened and more uneven flow of water by removal of
the organic matter and raising of water temperatures by ex-
80 Wisconsin Academy of Sciences , Arts and Letters
posure of the black stream bottom to the full sunlight. If the
stream is to be maintained at or near its present condition, all
cutting of trees from the headwaters swamp area should be
stopped.
Springs and spring-fed brooks are common in this region.
Brook trout have been observed to be very common in these
small brooks. No submerged aquatics, but semi-aquatic emergent
plants have been observed along the headwater brooks.
Principal plants of the headwaters brooks and springs in¬
clude: beaked willow, Salix Bebbiana ; bog willow, Salix pedi -
cellaris ; watercress, Radicula N asturtium-aquaticum (rather
rare in the valley) ; water horehound, Ly copus uniflorus ; speed¬
well, Veronica americana; tag alder, Alnus incana; true forget-
me-not, Myosotis scorpioides ; golden saxifrage, Chrysosplenium
americanum ; water hemlock, Cicuta bulbifera ; jewel weed, Zm-
patiens biflora ; and willow-herb, Epilobium adenocaulon .
Alder Swamp Association
In the upper region the Prule River meanders through the
white cedar and spruce bog with a zone of alder swamp associa¬
tion fringing it and varying in width from almost lacking, so
that the conifers come to the waters edge, to several rods. A
few meadows are located in this region. These are mainly domi¬
nated by bluejoint, Calamagrostis canadensis . Tag alder, Alnm
incanaf is the dominant plant of the alder swamp association
and covers the stream in the narrow places making it difficult
to get a boat through. Other shrubs which occur frequently are
highbush cranberry, Viburnum opulus var. americanum ; buck¬
thorn, Rhamnus alnifolia ; and red-osier dogwood, Comus sto -
lonifera . Other plants observed in the alder swamp zone in¬
clude : water hemlock, Cicuta bulbifera ; water arum, Calla pains-
tris ; and golden saxifrage, Chrysosplenium americanum on ex¬
posed mud banks at the base of the alders. In more open spots
with greater exposure to the sun, especially in such places as
along the edge of the meadows, several additional species of
plants are observable along the banks. These are termed the
Myrica Gale association in F. C. Gates9 paper on the bogs of
northern lower Michigan but are too limited in extent here to be
more than components of the alder swamp association. These
plants include: sweet gale, Myrica Gale; meadow-sweet, Spiraea
Thomson— Aquatic Plants and Flora of the Brule River 61
mlicifolia ; dock, Rumex Britannica ; meadow-rue, Thalictrum
dasycarpum ; crested fern, Dryopteris cristata ; jewel weed, im-
patiens biflora; bedstraw, Galium Glaytoni ; water horehound,
Ly copus americanus ; mint, Mentha arvensis var. lanata ; and
Iris, Iris versicolor .
Bluejoxnt Meadow Association
( Galamagrostis Association)
The “meadows'1 or open grassy places in the upper Brule
valley are in openings near the stream and vary from very small
areas to several acres in extent. The dominant plant in most of
these is blue joint, Galamagrostis canadensis , but other species of
plants may locally dominate. In one such area near County
Highway P crossing of the Brule, T.45N., R.11W., S.9, the domi¬
nant is fowl bluegrass, Poa palustris . Other plants character¬
istic of the Galamagrostis meadow association are niggerhead
sedge, Carex stricta ; chickweed Stellaria longifolia ; tufted loo¬
sestrife, Lysimachia thyrisifolia ; marsh harebell, Campanula
aparinoides ; tearthumb, Polygonum sagittatum , great St.
John's-wort, Hypericum Asycion ; marsh St. John's wort, Hyper¬
icum virginicum var. Fraseri ; water horehound, Ly copus ameri¬
canus; and mint, Mentha arvensis var. lanata. Gates ( loc . cit.)
suggests that such meadows are due to burning. It has not been
ascertained whether or not this is the case along the Brule. No
stumps were observed in the “meadows" such as would be ex¬
pected following fires.
Aquatic Plants in Upper Brule
Aquatics in the upper section of the stream which run
through the alder and white cedar associations are few in num¬
ber. Wild celery, Vallisneria amsricana , and bur-reed, Spargan-
ium angustifolium are the most abundant. The bottom in this
section Is mainly covered with a black organic mud largely com¬
posed of remains of diatoms and higher plants (material ex¬
amined by N. C. Fassett and R. I. Evans). In the broader pools
at the turns in the stream the higher aquatics are more common
than in the narrow stretches between the meander curves, where
the alders overhang the stream and a passageway for boats is
maintained only by cutting. Probably shading by the alders and
the dark color of the water limits the aquatics in such sections
of the stream. Watermoss, Fontinalis antipyretica var. gigantea ,
Table I. Brule aquatics.
62 Wisconsin Academy of Sciences , Arts and Letters
Thomson — Aquatic Plants arid Flora of the Brule River 63
Spargqnium fluctuans
Spirodela polyrhiza
Ty^ha latifolia
ValHsneria ameWcana
Zizania aquatica
64 Wisconsin Academy of Sciences , Arts and Letters
is frequent in small clumps on rocks or, more often, on the sub¬
merged lower parts of the branches of the alder. A few plants
of pondweeds, Potamogeton tenuifolius and P. obtusifolius , were
seen. At one place where beaver had erected a dam and the
bottom was sandy a few plants of water starwort, Callit riche
palustris were observed. Duckweed, Lemna minor , is repre¬
sented as scattered plants, mainly in the slow waters along the
edges of the stream.
From the bend just above the Stone cabin above Stone’s
Bridge to the confluence of Nebagamon Creek with the Brule
River is the section of the river with the greatest abundance of
the higher aquatic plants. This region has been cleared out for
the most part so that there is little obstruction of the stream by
the alder swamp association or by fallen white cedar or spruce
from the swamp conifer association. Artificial obstructions have
been placed in the stream in the form of deflectors, wing dams
and structures of like nature for the purpose of improving the
stream for fishing. The stream is exposed for the most part and
does not have the cover and shade of the upper section from the
crossing of County Highway P to the crossing of County High¬
way S. Greater velocity in some sections gives sandy bottom and
boulders in the rapids but there are also large stretches, par¬
ticularly at the spreads called Big and Lucius Lakes in which the
river is dropping muck, largely of organic nature. Conditions in
this section of the stream seem, on the whole, to be excellent
although a certain amount of cover might be desirable to reduce
the insolation of the dark colored bottom which raises stream
temperatures on clear days. The “spreads” or lakes are an es¬
pecial problem. If it is desired to reduce the area of bottom
exposed to direct sunlight it is possible that the planting of wild
rice would be successful. Owen, in 1848, reported wild rice in
abundance in “First and Second Flag Lakes” or Big and Lucius
Lakes. None was observed to be at present growing in these
lakes. Wild rice was observed only in the slough at the mouth
of the Brule. Apparently dredging operations eradicated the
wild rice formerly growing in these lakes. The conditions seem
especially favorable for such an establishment.
In the section of the stream from the big bend just above
Stone’s Fridge to Big Lake the higher aquatics are abundant.
Above Stone’s Bridge the dominants are bur-reed, Sparganium
T hO'Mson—. Aquatic Plants and Flora of the Brule River 65
angusti folium; pondweed, Potamogeton obtusifolius , P. ienui-
folius and water crowfoot, Ranunculus longirostris. Arum,
Ccdla palustris, is frequent along the border of the stream. Just
below the bridge at Stone's Bridge there may be added to these
species the following: water crowfoot, Ranunculus trichop hyU
lus ; waterweed, Anacharis canadensis; watermoss, Font mails
antipyretica var. gigantea , and a very considerable amount of
Spirogyra and Hydrodictyon of the algae. In August and Sep¬
tember the filamentous algae appeared in great abundance, long
streamers extending downstream, some of them being many
yards in length. The condition of these algae in a considerable
portion of the stream did not appear healthy to the casual ob¬
server. Some investigation of the abundance of these algae, the
reasons for it, the poor appearance, and the possible effect on the
fish and other life in the river ought to be initiated. Richardson's
pondweed, Potamogeton Richardsonii , appears in the river in
abundance fairly far down near McDougal's Springs. The domi¬
nant aquatic in this section of the stream is the Anacharis . It is
in great abundance, usually over sand or sand and muck bottom.
At McDougal's Springs, the river widens somewhat and the
slower current drops a quantity of organic material as wTell as
sand. In this broader stretch in the river, sago pondweed, Pota¬
mogeton pectinatusy and floating-leaf pondweed, P. natans , are
abundant.
Potamogeton natans persists down the river to the Pierce
Estate bridge then reoccurs in the slough in an old oxbow at the
mouth of the river. Just above the boathouse of the Pierce Es¬
tate there is an extensive bed of Potamogeton Berchtoldi var.
mucronatus (P. pusillus of most manuals) on a sandy bottom.
This is the only place in which it occurs in the river.
In the broad stretch recently called “Sucker Lake", but
known as the third Flag Lake in early reports on the region, the
stream widens out into a shallow stretch flowing over sand con¬
taining a small percentage of organic material. In this section
Richardson's pondweed is the dominant and there is a little each
of sago pondweed; pondweed, P. oblongifolius ; and water mil¬
foil, Myriophyllum exalbescens.
Big Lake and Lucius Lake have very similar aquatic floras.
In Big Lake there appears to be a zonation based upon depth of
wafer. At the head of the lake is a sandy stretch with shallow
66 Wisconsin Academy of Sciences , Arts and Letters
water. Here the principal aquatics are: water weed, Anacharis
canadensis ; Richardson's pondweed ; sago pondweed ; and water
crowfoot, Ranunculus trickophyllus. Water star wort, Callitriche
hermaphroditica (C. autumnalis) is not noticeable in the sum¬
mer, but in September and October appears in abundance in the
sandy area at the head of Eig Lake, preferably in slower moving
water where a little organic matter has settled in the irregular
depressions of the bottom. Deer were observed to browse on the
aquatics in the shallow water at this end of the lake. It is not
certain what influence they may have on the ecology of the
aquatic plants in this section of the stream.
In Big Lake the water slows up so that there is almost no
current. The deeper portion appears to be toward the east shore
and the shallow water is on the west shore over a broad, gradu¬
ally deepening bank of largely organic mud. In the shallow
water, up to two feet in depth, the dominant aquatic is leafy
pondweed, Potamogeton foliosus var. macellus. From this depth
to about six to eight feet there is an abundance of a large num¬
ber of species: Richardson’s pondweed, Potamogeton Richard-
sonii ; Muskie weed, P. praelongus ; pondweed, P. tenuifolius;
pondweed, P. obtusifolius ; sago pondweed; flat-stemmed pond¬
weed, P. zosteriformis ; waterweed, Anacharis canadensis ; horn-
wort or coontail, Ceratophyllum demersum ; water milfoil, Myr-
iophyllum exalbescens ; and water crowfoot, Ranunculus longi -
rostris.
Lucius Lake has a very similar flora to that in Big Lake and
the conditions are very similar, with a sandy shallows at the
head of the lake, grading into soft organic mud in the major
portion of the lake. Aquatics collected or observed here include :
Potamogeton Richardsonii, P. praelongus , P. obtusifolius , P.
pectinatus , P. zosteriformis , Ceratophyllum demersum , Ana¬
charis canadensis and Myriophyllum exalbescens . In the shallow
water over the mud bottom, Potamogeton foliosus var. macellus
is again dominant.
The banks of Big and Lucius Lakes are lined at each end by
narrow strips of the white cedar association, similar to the
swamp above the lakes. The white cedar shows excessive brows¬
ing by deer, the browse line being very evident (Fig. 5). The
major portion of the bank is approached by the white birch and
aspen association but here, as along the rest of the river, a nar-
Thomson — Aquatic Plants and Flora of the Brule River 67
row fringe of the alder swamp association grows at the water's
edge.
From Winneboujou to the mouth .of Nebagamon Creek the
stream is fairly uniform in character, a series of rapids over
bouldery bottom alternating with the sandy stretches. Higher
aquatic plants are confined to the sandy areas. Richardson's
pondweed, Potamogeton Richardsonii ; water crowfoot, Ranun¬
culus trichophyllus ; and waterweed, Anacharis canadensis are
the principal species present. Smaller quantities of water mil¬
foil, Myriophyllum exalhescens; Potamogeton tenuifolius ; and
sago pondweed, P. pectinatus were observed. In the fourth pool
below Winneboujou a small amount of starwort, Callitriche her-
maphroditica , the second station in the river, was observed. The
banks through this section have a complex flora but the dominant
plant along the river bank is the tag alder. An abundant herb,
forget-me-not, Myosotis scorpioides , lines the bank especially in
springy spots. Black ash and American elm are abundant along
the bank. Other trees overhanging the water include white
birch, Norway and white pines, white spruce, balsam fir and
small-toothed aspen.
i
Aquatic and Bank Flora in Middle Brule
Below the junction with Nebagamon Creek the stream as¬
sumes a placid, winding character as far as the head of Little
Joe Falls above the Ranger Station. Here very few aquatics
were to be found. The bottom was heavily silted, but even in the
sandy stretches only small colonies of aquatic plants were ob¬
served. In this section of the stream Potamogeton tenuifolius ;
sago pondweed, P. pectinatus ; water milfoil, Myriophyllum ex¬
alhescens ; waterweed, Anacharis canadensis ; and water crow¬
foot, Ranunculus trichophyllus were observed. The dominant
bank plant is the tag alder. Elms of large size and black ash
are also very common here. A small bluejoint, Calamagrostis
canadensis , meadow is along the stream bank. St. John's wort,
Hypericum Ascyron ; tearthumb, Polygonum sagittatum ; hore-
hound, Ly copus americanus ; and mint, Mentha arvensis var. la-
nata were collected in this meadow but are probably of no im¬
portance to the stream life as they are insignificant in number.
No aquatics were noted in the rapids past the Ranger Station.
Below the Ranger Station the Brule becomes a sluggish
stream, meandering through muddy bottoms from T.47N.,
€8 Wisconsin Academy of Sciences , Arts and Letters
R.10W., Sec. 23 to just above Co-op Park, T.48N., R.10W.,
See. 26. Silting is very heavy in this section as it is in the clay
belt. With this heavy silting and a fine clay-silt bottom, aquatic
plants and probably also many forms of animal life find condi¬
tions very unfavorable. The principal aquatics in this section,
Richardson’s pondweed, Potamogeton Richardsonii; waterweed,
Anacharis canadensis; and water crowfoot, Ranunculus tricho-
phyllus , grow only in a narrow strip toward the edges of the
stream. No aquatics were observed in the center. In shallow
water on mud banks, arrowheads, Sagittaria rigida and S. lati-
folia /. hastata are common. One mud bank with a foot of water
over it, a short distance below the weir at the Ranger Station,
had a few plants of a pondweed, Potamogeton obtusifolius var.
rutiloides growing on it, associated with the ribbon-leaved sub¬
merged form of Sagittaria rigida . Along the banks the ubiqui¬
tous alder swamp association is dominant next to the water, but
the river bottoms are dominated by large American elm and
black ash trees. Many of these overhang the stream and may
contribute insects and other fish foods to the water below. Wil¬
lows are comparatively uncommon along the Brule and are in-
sigificant as bank plants. Slender willow, Salix petiolaris ; shin¬
ing willow, S. lucida ; white willow, S. alba ; sandbar willow, S .
interior; and near cottages, golden osier; S. viminalis are the
common willow species along the lower reaches of the Brule.
The shrubby species, shining willow, S. lucida , has much to re¬
commend it for bank erosion prevention in the clay soil area. It
grows at the very edge of the water, leaning over the stream,
and produces an abundance of water roots which help prevent
stream erosion of the banks. It appeared to grow best in the
heavy clay soil. None of the other species of willow observed in
the lower reaches of the Brule approached as far into the stream
nor showed such root development as this species. The tag alder
and red-osier dogwood are the dominant bank species.
Aquatics and Bank Flora in Lower Section of the Brule
A short distance above Co-op Park, T.48N., R.10W., Sec. 26,
the stream begins the series of rapids which, alternating with
short, quiet pools, continues to about three-quarters of a mile
from the mouth of the river. Except for a very few places be¬
tween Co-op Park and Highway 13 bridge there are no higher
aquatic plants in the river. One small patch of waterweed, Ana-
Thomson^— Aquatic Plants and Flora of the Brule River 69
dmris canadensis , and a patch each of pondweeds, Potamogeton
tenuifolius , P. epihydrus , and P. obtusifodus were all that were
observed. They were in eddies in the stream on a muck bottom,
six inches to a foot under water. The filamentous algae, Clado -
phora and Oedogoniumf clinging to the rocks in the rapids where
the velocity of the stream was such as to prevent deposition of
the silt burden, were the only conspicuous plants. The stream
is yellow with silt and erosion of the vegetation by the silt in
suspension in the water must be a considerable factor in the
ecology. The banks in this section are dominated by alder but
many other plants contribute to the cover for fish food in the
stream.
The most abundant bank cover plants in addition to the alder
are: balsam poplar, Populus Tacamahacca ; white birch, Betula
papyrifera ; white spruce, Picea canadensis ; white pine, Pinus
strobus ; willows, Salix sp. ; red-osier dogwood, Cornus stoloni-
fera; white cedar or arbor vitae, Thuja occidentals ; red maple,
Acer rubrum ; elm, Ulmus americana ; balsam, Abies balsamea;
and black ash, Fraxinus nigra . Also observed in minor amounts
along the banks were : shadbush, Amelanchier canadensis ; high-
bush cranberry, Viburnum opulus var. americanum ; and Vir¬
ginia creeper, Parthenocissus vitacea . Numerous small grassy
patches, largely Calamagrostis canadensis and Glyceria grandis ,
were interspersed with the alder. These were often bordering
the water and may influence the insect food supply falling into
the stream.
The banks all through this clay soil country show evidences
of slumping into the stream. Apparently the bank is undercut
by the stream and seeping water above the bank causes a large
landslide to slump down, gradually losing its base by stream
erosion, the trees often remaining upright on the slumping sur¬
face. There are numerous examples of all stages of this slump¬
ing along the lower course of the Brule from Co-op Park to the
mouth.
The activity of these banks seems to have been accelerated in
recent years, possibly due to removal of the forest cover by
pulpwood cuttings and lumbering. David Dale Owen, passing
through this territory in 1848, made especial note of a landslide
of twenty to twenty-five feet in depth at a distance of about
fourteen miles from the mouth of the river. If his observations
70 Wisconsin Academy of Sciences , Arts and Letters
were accurate, it would be supposed that the slumps are much
more common now. (Table 3.) If there are lenses of water¬
bearing gravels in the clay soil at the head of these slumps, a
possibility suggested by Mr. E. F. Bean, State Geologist, it may
be difficult to stop the slumping. Diversion channels or drains
may be necessary to divert these waters. Piles of green white
cedar driven into the slumping mass near the base may hold it.
Willows, such as shining willow, Salix lucida , may help in slow¬
ing the undercutting of the stream edge. Some of these banks
are undercutting rapidly enough to show a yellowing of the
stream below the bank as it removes the clay. The banks below
N. P. Johnson bridge and the Highway 13 bridge are of this
rapidly slumping character. On the watershed above the stream
it will be necessary to institute soil erosion control practices,
particularly on the cultivated soils and along the roadsides, the
chief contributors of the silt and colloidal clays which are so
detrimental to the lower course of the Brule.
At the mouth of the Brule and extending a short distance
upstream there is an abundance of a few species of higher
aquatic plants. These mainly are located on the shallow silt and
clay bottom on the stream side of the bar across the mouth and
extend in distribution up along the sides of the stream much in
the way in which these same species, which can apparently sur¬
vive heavy silting, extend along the sides of the stream below the
weir and down toward Co-op Park.
The abundant aquatics in the stream near the mouth include :
pondweed, Potamogeton obtusifolius ; Richardson’s pondweed, P.
Richardsonii ; waterweed, Anacharis canadensis ; and water mil¬
foil, Myriophyllum exalbescens . One specimen of yellow water
lily, Nuphar variegatum , was observed just above the bar at the
mouth. At the entrance to an abandoned oxbow slough upstream
from the mouth a large colony of sweet flag, Acorus calamus , is
growing together with cattail, Typha latifolia ; arrowhead, Sagit -
taria latifolia; great bulrush, Scirpus validus ; reed meadow
grass, Glyceria grandis; marsh cinquefoil, Potentilla palustris ;
and willow-herb, Epilobium adenocaulon.
The bank plants, here as along most of the river, are mainly
tag alder and red-osier dogwood. Slender willow, Salix petiolaris
and shining willow, S. lucida are frequent. A few trees of haw¬
thorn, Crataegus succulenta ; white willow, Salix alba ; and red
Thomson — Aquatic Plants and Flora of the Brule River 71
ash, Fraxinus pennsylvanica were mixed with the usual white
birch, balsam fir, white spruce, American elm, black ash, and
small toothed aspen. Smaller plants along the bank included
meadow rue, Thalictrum dasycarpum ; curly dock, Rumex cris-
pus ; swamp milkweed, Asclepias incamata; Joe-Py e-weed,
Eupatorium maculatum ; Aster lateriflorus ; blue joint, Calama-
grostis canadensis; nettle, JJrtica procera; and blackberry, Ru-
bus nigrohaccus . A large colony of sandbar willow, Salix inte¬
rior , exists about a quarter of a mile up the river but it is on an
old terrace rather than on the banks of the present course.
Ostrich fern, Pteretis nodulosat is common in an abandoned,
filled in slough in similar situations as it is found along the
stretch from Highway 2 to Co-op Park.
A stagnant slough exists in an abandoned oxbow at the
mouth of the Brule River. This slough is rich in aquatics, in¬
cluding a number of species not observed elsewhere along the
river. Wild rice, Zizania aquatica , and floating-leaf pondweed,
Potamogeton natans , are abundant. Other common aquatics in¬
clude: large-leaf pondweed, Potamogeton amplifolius ; coontail,
Ceratophyllum demersum; milfoil, Myriophyllum exalbescens ;
bur-reeds, Sparganium eurycarpum; S. fluctuans; S . chlorocar -
pum ; water marigold, Megalodonta Beckii; yellow water lily,
Nuphar variegatum ; marsh cinquefoil, Potentilla palustris ; cat¬
tail, Typha latifolia; and softstem bulrush, Scirpus validus . An
abundance of purple-fringed Riccia, Ricciocarpus natans , floats
on the water between the stems of the emergent aquatics. The
common duckweeds, Lemna minor and Spirodela polyrhiza , are
much less common in this slough. During periods of high water,
the river may partially drain through the slough, giving a light
flow through and across the bar, opening a second mouth to the
west of the major mouth of the stream. This second mouth was
being used in the fall of 1942 by the river, a shallow flow cross¬
ing the bar near the high western bank at the mouth.
Mud Bank Associations
No one species of plant seems to be especially characteristic
of the mud banks along the river. In the upper Brule, above
Stone’s Bridge, there are a few species growing sparsely inter¬
spersed among the alders in the alder swamp association. These
are golden saxifrage, Chrysosplenium americanum ; water hem¬
lock, Cicuta bidbifera ; water starwort, Callitriche palustris ; and
72 Wisconsin Academy of Sciences , Arts and Letters
Table II. Mud bank association.
willow-herb, Epilobium adenocaulon. Farther downstream be¬
tween Stone's Bridge and the Pierce Estate bridge the same
species exist ; but on two different mud banks, in the channel but
located to one side of the main water flow, are fair-sized colonies
.of cattail, Typha latifolia, and bur-reed, Sparganium chloro -
carpum var. acaule . In Big Lake, or second Flag Lake, along the
west side there are several grassy “islands" some of them being
solid enough to stand on. These latter have a sandy soil mixed
with a large percentage of organic muck. On these are the great¬
er number of the species included in Table 2. Other “islands"
are based on the soft organic sediments in the lake. The plants*
Thomson — Aquatic Plants and Flora of the Brule River 73
mainly rice, cut-grass, Leersia oryzoidesf compose an almost
floating mat. Tickseed, Bidens cemua , is included in the same
habitats. Farther down the river in the sluggish sections below
the mouth of Nebagamon Creek and down almost to Co-op Park
there are numerous muck and clay banks deposited along the
shores of the stream and in the mouths of abandoned oxbows.
The most characteristic plants of these habitats are the arrow¬
heads, Sagittaria species, but others listed in Table 2 are also
common. The vervain, Verbena hastata, and lovegrass, Eragros -
tis hypnoides, seems to prefer sandier banks and shores than the
other species. Mud banks are scarce through the section of the
Brule which descends the lower rapids to the mouth. Near the
mouth, mud banks reoccur and a few species were observed.
These were: cattail, sweet flag, softstem bulrush, and willow-
herb.
Table III.
Conspicuously eroded banks along the river
(determined by photo examination)
T.49N., R.10W., Sec. 15-SE corner of NWy4 — back from river a little vegeta¬
tion on top of west bank.
-center of SW corner of NE1/^— -narrow slip-bank; vege-
tion on top near base.
West bank.
-SW corner of NWY4 of SEy*, — very large, directly on
river. Along west bank.
-South side of Ny> of SEy*— long slip bank on N side
of river. (Tlv's is gener¬
ally east shore.)
Sec. 22-SE comer of NE% of NW*4 — small incipient slump be¬
gun.
-NW Y4 and NE14 of SEVi — 2 small eroded faces along
river.
-SWV4 of SEH — one long slumo.
Sec. 27 — NWy4 of NE*4 — no slumping but bad wash near cul¬
tivation on top of both banks. There
is very bad erosion observed from
ground along the road cuts on both
sides of the river.
Sec. 34-West side of NEV4 of NEV4 — bad slump.
-East side of NWV4 of NEy4 — bad slump.
-NE corner of SWV4 of NE14— ’ncipient slump.
-East side of NE!4 of SE% — 2 bad slumps just below
Hwy. 13 bridge. The south
one is very severe.
74 Wisconsin Academy of Sciences, Arts and Letters
T.4SN., R.10W., Sec. 3-NW comer of SE% — Large slump. West side river.
Sec. IO-NE14 of SEy4 — incipient slump. East side river.
-NWV4 of SEV4 — very bad slump. West side river.
-SWy4 of SE1/4 — severe slump.
Sec. 15-NWV4 of NEy4 — west bank — slump.
-SWy4 of NEy4 — west bank small slump.
-NWy4 of SEy4— west bank — very large slump.
-SE corner of SW^4 of SE% — very severe slump just
below N.F. Johnson’s
Bridge. West bank.
Sec. 23-NWyj of SWy4 — incipient slump. Vegetation near river.
West bank.
-SEJ/4 of SW% — slump bank, vegetation line along
river. East bank.
Sec. 26-NE comer of NEy4 of NWy4 — Slump with line of veg-
etat.on along river. East
bank. *
Sec. 35-South side of NW% of SEy2 — slump bank.
T.47N., R.10W., Sec. 2-SW14 of NE% — 2 very large slumps.
Sec. 14-SEy4of SWy4 — by Yale’s cottage. (Does not show from
air.)
-East side of NEy4 of NWy4 — large severe slump.
Recommendations
In the management of the Brule River as a trout stream it
appears that the following recommendations would help in main¬
taining the present condition of the stream and in improving it
somewhat :
1. Stop all cutting of timber in the headwaters swamp area.
Allow no cutting from crest to crest of the valley and from
St. Croix Lake to Winnebou.iou.
2. Allow alder swamp association cover to resume growth over
the upper section of the stream from Stone's Bridge to the
Pierce Estate bridge.
3. Do not remove fallen timber from the headwaters swamp
area. It is an essential part of the forest floor, going to form
the five to six feet thick layer of woody peat which overlies
the outwash sands of the valley floor. In addition it becomes
the habitat of many species of plants as it decays. The snags
falling in the stream should not be removed more than neces¬
sary to allow a narrow passage for boats.
4. Refrain from placing “improvements” in the headwaters
swamp area. These are certain to react detrimentally upon
the forest by drying and deterioration of the organic soil.
Thomson — Aquatic Plants and Flora of the Bride River 75
5. If it is desired to narrow the expanse of Big and Lucius Lakes
which is exposed to direct insolation, the planting of vegeta¬
tion such as wild rice, and yellow water lily may assist in
accomplishing this aim. Native species .of plants should be
used rather than exotics.
6. Control of pulpwood lumbering appears to be necessary on
the slopes in the lower valley to reduce the heavy silting of
the river and slumping of the banks. A wide belt extending
back from the stream edge, somewhat further than the edge
of the incised recent erosion banks, should be left entirely un¬
disturbed by unwise roadside maintenance, cultivation, or
lumbering.
Erosion control practices are necessary in the Lake Nebaga-
mon-Nebagamon Creek drainage section and the lower valley
from the region of the mouth of Nebagamon Creek north¬
wards.
8. Anchorage of the slipping and badly eroding banks in the clay
belt area is necessary to reduce the silting of the lower river
which suffocates and erodes aquatic life. This may be done in
part by living white cedar or arbor vitae stakes, willow plant¬
ing (preferably using native species), and slight diversion of
the stream. No major alteration of the course of the stream
is recommended.
i. Control erosion from the highway ditches and banks draining
Into the river.
Summary
In a reconnaissance survey of the larger aquatic plants and
bank flora of the Brule River it was found that there are three
major ecological sections of the stream. The upper section has as
Its dominant bank associations the alder swamp and coniferous
swamp associations. Few aquatic plants are found in the un¬
changed portion of the stream; many are listed for the altered
portion through the coniferous swamp and for the two large
spreads or “lakes.” The middle section bank flora is mainly
alder and a bottomland flora of elm and ash. The aspen associa¬
tion is characteristic of the uplands in the middle section. Few
higher aquatic plants are found in the middle section of the
river. The lower section, largely flowing through a clay-soil belt,
has very few aquatic plants, probably because of the heavy bur¬
den of silt in the water. The bank flora of the lower section of
•76
Wisconsin Academy of Sciences , Arts and Letters
the river is varied and includes a mixture of conifers and de¬
ciduous trees as well as the abundant alder. The lower course
of the river is in the worst condition. Recommendations for im¬
proving the stream condition to maintain a trout population are
made.
Literature Cited
Bean, E. F.
1945. Topography and Geology of the Brule River Basin. Trans. Wis.
Acad. Sci. 36:7-17.
Bordner, J. S.
1933. Land Economic Inventory of Douglas Co., Wis. Forest and Generali
Cover Map.
Fassett, N. C.
1940- Manual of Aquatic Plants. McGraw Hill.
Gates, F. C.
1942. The Bogs of Northern Lower Michigan. Ecological Monographs 12:
213-254.
Owen, David Dale.
1848. Geological Reconnaissance of the Chippews Land District Senate
Executive Doc. 57:58-61.
Plate 2. Bluejoint, Calamagrostis canadensis, meadow on upper Brule. Sec. 2,
T.45N, R.11W.
Plate 1. Looking eastward across the upper Brule valley. Pin Cherry and
Aspen association in front. White Cedar, Black Spruce and Balsam in the
Thuja association in the valley. Sec. 3, T.46N., R.11W.
Plate 3. Vegetation along a tributary of the upper Plate 4. Alder swamp association in the upper
Brule. Salix bebhiana on the left, Calamagrostis Brule valley. Sec. 3, T.46N., R.11W,
canadensis on the right, Alnus incana in the back.
Wilson’s Fork, Sec. 33, T.46N., R.11W.
Plate 5. Browse line in Thuja association at the upper end of Big Lake.
Sec. 15, T.46N., R.10W.
Plate 6. The west shore of Big Lake. Note the very narrow fringe of Thuja
association with Spruce. Aspen and White Birch approach close to the lake
Sec. 10, T.46N., R.10W.
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Plate 9. Rapids west of Waino. Sec. 15. T.48N., R.10W. Forest of mixed
Birch. Balsam. White Pine. Elm Poplars. Alder along stream edge. April.
1944.
Plate 10. Eroding bank below N. P. Johnson Bridge. Sec. 15, T.48N., R.10W.
Popple-Birch association on hillslope. April, 1944.
Plate 11. Section of slumping bank below N. P. Johnson Bridge showing
large mass moving down into stream. Recent drop of more than a foot
showed along the line where the man is standing.
Plate 12. Aspen-Birch association. Brule River, looking north or downstream
from Highway 13 bridge. Sec. 34, T.49N., R.10W.
Plate 13. The lower Brule Vs mile above the mouth, Alder swamp and
“meadows” fringe the stream. Sec. 10, T.49N., R.10W.
Plate 14. The mouth of the Brule from the stream side. Note the sandbar
almost closing the mouth. Alder, Dogwood and Willow border.
Plate 15. The mouth of the Brule from the high east bank, Aspen in the fore¬
ground. Note the stagnant slough against the west bank in the left of the
photo.
THE QUAIL IN EARLY WISCONSIN
A. W. SCHORGER
The quail ( Colinus v. virginianus) has always been the most
popular of American gamebirds. On autumn days, its rapid
flight, preceded by an explosive rise, invokes the skill of the
sportsman. The quail’s gentle, confiding habits appeal to the
layman, and the flavor of its flesh to the epicure. The name,
bob-white, used by scientists has not gained headway with the
masses who are the final arbiters in terminology.
The quail within a period of ten years, 1845-1854, became
extraordinarily abundant in Wisconsin. It then declined in num¬
bers so rapidly that during the past 75 years the most that can
be said for the species is that it has maintained its existence.
There is a fascination in the study of wildlife populations when
inquiry is directed to final causes. Taking into consideration all
the known influential factors, a decade of favorable winter
weather seems to have been of the most importance in producing
the peak in the population. Unless we assume that weather has
continued to be the important factor, the question of why the
quail refuses to undergo more than a sporadic increase remains
unanswered. The one certainty is that the factors controlling
the quail population are more subtle than was suspected for¬
merly.
Original Range
Among the bones recovered from the Indian village site at
Aztalan, Jefferson County, Somers (1) reported those of the
quail. The identification should be checked by a competent oste¬
ologist. Theodore Rodolf (2) and Charles Rodolf (3) came to
Lafayette County in 1834, when it was in a primitive condition,
and both have stated that quail were abundant at that time.
Three years later Gen. Smith (4) travelled in southwestern Wis¬
consin and wrote: “. . . the partridge or quail is not often met
with. I saw three or four near some farms and as this bird
always follows and attends cultivation, the flocks will certainly
increase with the opening of farms and the raising of grain.”
77
78 Wisconsin Academy of Sciences, Arts and Letters
The quail at times must have been distributed widely
throughout the open areas of the state. (Fig. 1.) Featherston-
haugh (5) ascended the Fox River in 1835 and found the “plain¬
tive quail” in the southwestern corner of what is now Winnebago
County. Hank Tourtolatt, an Indian trader, in the spring of
1849, made a claim at Weyauwega, the first for the Waupaca
River. He spent the summer “catching fish and shooting quails.”
(5a) The Menominee Indians, in October, 1847, received their
payment at Pauwaygan [Poygon] Lake, twenty-five miles north¬
west of Oshkosh and ten miles from the habitation of any white
men. They furnished for the occasion large quantities of game
Schorger — The Quail in Early Wisconsin 79
including quail (5b). In June, 1829, Mrs. Mary Bristol (6)
attended a wedding at Grand Kaukaulin (Kankauna, Outagamie
County) . She mentions quail as part of the wild meat served for
supper. H. Pratten (6a) listed the quail for northern Wisconsin
and Minnesota but this is of no assistance in determining the
range since he is indefinite on localities. The last survey was
made in 1849.
The quail is not a conspicuous bird and would be overlooked
easily by the casual observer, particularly during the summer.
It is therefore not surprising that conflicting statements are
encountered. Keyes (7) came to Jefferson County in 1837 and
stated that at that time there were no quail or rabbits, due pre¬
sumably to the presence of wolves and foxes. Cravath, (8) writ¬
ing of the winter of 1839-40 at Whitewater, states also that quail
were unknown then; however, Mrs. Freeman L. Pratt, (8a)
who came to Whitewater in 1837, mentions that they were then
plentiful and that quail-pies were served at the raising of the
frame of a flour mill in June, 1839. It is also stated that in the
spring of 1840 "much sport was to be found in the pursuit of the
smaller species of game, such as quails, grouse, ...” (9) A Brit¬
ish traveller (10) shot some quail near Astalan in the fall of
1841.
The quail, as a Wisconsin bird, was mentioned by Lapham
(11) in 1844. Major Tenney (12) came to Madison in 1845 when
it was common practise to hunt quail and prairie chickens on the
square of the capitol. Quail were present in the town of Tay-
cheedah, Fond du Lac County, in 1838, when the first settlers
arrived (13). Within a few years they became numerous. In
the fall of 1851, Capt. Mackinnon (14) drove from Sheboygan
to Fond du Lac. Quail were among the birds "constantly ex¬
posing themselves.” The Titus family settled about 1853 in the
wooded section east of Fond du Lac, when quail were numerous
"but so easily approached by the hunter that they soon grew
fewer in number (15).” Ficker (15a) came to the town of Me-
quon, Ozaukee County, in the fall of 1848. He wrote that the
"partridges are not much bigger than the German quail. . .
The presence of quail was certainly not dependent on agri¬
culture. Quarles (16), in his letters from Southport (Kenosha)
in 1837-1843, does not mention the quail but only the kinds of
game killed with his rifle. He wrote in 1838 that it is about
80 Wisconsin Academy of Sciences, Arts and Letters
three years since the first settler arrived. Mrs. L. T. Fowler (17)
came to the town of Bristol, Kenosha County, in 1887, when
“quail and prairie chicken were abundant.” Another immigrant
(18) wrote from Southport on December 19, 1842, that game,
including quail, was plentiful. It was said of the town of East
Troy, Kenosha County, in 1845 : “Small tracts of land were un¬
der cultivation but the autumnal fires still swept through the
woods. . . . Then the sweet wild plums grew in the thickets
where covies of quail were hidden (19).”
Quail were found at Waukesha by Chapman (19a) when he
arrived in the spring of 1841. Breck (20) flushed several covies
of quail near Nashotah in November, 1846, and mentions that
in 1841 there were few settlers inland from Lake Michigan.
Beginning with 1846, quail are mentioned as abundant in
several localities. Near Milwaukee the species was “never so
abundant,” and it is added : “The increase of Quails in particular
seems to keep pace with the rapid growth of our population and
the spread of the settlements.” In October they were shot in the
center of the town (21). It was now common in Walworth
County (22). Quail were abundant in August, 1847, at Madi¬
son (23) and Watertown (24), and they were hunted at Prairie
du Chien (25). Their abundance in the Milwaukee (26) market
“would excite an enthusiasm among eastern epicures.” In a
letter dated December 19, 1848, Biihler (27) mentions the rapid
increase in the number of quail at Prairie du Sac, many being
shot and netted in the cornfields. There were only six resident
families at this place in 1840.
Extension Northward
The statement of Barry (28), made in 1854, that the quail
was “distributed in immense numbers over the entire state” is
much too broad. It is not certain that the original range in the
Mississippi Valley extended above La Crosse. The following in¬
teresting note was printed at Hudson, St. Croix County, in July,
1855 : “In riding across the prairies, a few days since, in a west¬
ward direction from this place, we frequently started up a bevy
of quails from the road-side. Judging from the numbers we saw,
we conclude that next fall sportsmen will find quails here in great
plenty, a desirable recent addition to the game of this section of
the country.” In August, they were listed among the birds ob-
Schorger — The Quail in Early Wisconsin 81
tamable in “unlimited numbers” (29). If quail were so plentiful
there in the summer of 1855, it is beyond belief that they did not
occur some years earlier.
Quail were mentioned as quite plentiful at Wausau (30) in
1868. They arrived at Ashland (31) in 1874, and at Superior
(32) in 1882. An Ohio hunter, familiar with the species, re¬
ported seeing a flock of thirteen on November 14, 1891, near
Florence, Florence County (33).
Period of Abundance
Quail became plentiful by 1846. In 1852 they were brought
into Madison (34) “by the bushel” ; and at Prairie du Chien (35)
they were never so plentiful. Emery (35a), who came to the
town of Rutland, Dane County, in 1852, said: “I have seen
thousands of quails (Bobwhite) come into my father’s yard to
get the seeds from his millet hay.” During this year Hoy (36)
wrote that the quail, within a few years, had become remarkably
numerous. They were so abundant by 1853 as to invade Madi¬
son (37) in force, flying against buildings and breaking win¬
dows. All the old muskets were brought into action. Some of
the citizens were so intolerant as to object to being shot in the
back. Quail were so plentiful in central Wisconsin that it had
“ceased to be sport to shoot them” (38). In Milwaukee they
usurped the place of wild pigeons, and were used for trap shoot-
ting (39). Waukesha (40) had “huge quantities” of quail and
prairie chickens.
The peak in population was reached in 1854. Quail were as
abundant as ever at Janesville (41) in spite of the number
trapped the year previous; and more numerous than usual at
Watertown (42) and Jefferson (43). At Madison (44), “quail
are now found in every grove, and a good shot can readily bag
50 to 75 in a day.” They were plentiful even as far north as
Green Bay (45).
Despite the shipment of enormous numbers of quail during
the fall and winter of 1854-55, they were still abundant in 1855.
In January it was said: “Quails have never been in greater
abundance in Wisconsin. . . .” (46) They were plentiful in the
fall at Milwaukee (47), and were shot in the heart of the city.
They were plentiful also at Elkhorn (48), Waukesha (49), Wa¬
tertown (50), and Hudson (29). Quail could be shot “almost
82 Wisconsin Academy of Sciences , Arts and Letters
anywhere” at Madison (51), while the following forceful state¬
ment appeared at Jefferson: “We saw about a million — say nine
hundred thousand — in a short trip the other day. We found one
quail-trap full, and let the poor things out.” At Portage there
were brought in “rabbits, quails, etc. beyond enumeration” (53).
It is difficult to conceive of the former abundance of quail.
They were so numerous at times at Milwaukee that there were
“on an average, three bevies to every ten acre lot” (54). It was
said that at Madison “a ten-minutes walk enables you to put up
your first bevy of quails while every succeeding five minutes
furnishes a fresh covey” (55). The narrow strip of land be¬
tween the lakes at Madison was a funnel through which passed
great numbers of birds during the irruptions. The following
facetious account is not as exaggerated as it seems: “Yes, in
early days, if you wanted a meal of quails — all you had to do was
to take a club and let fly once or twice among the tall grass in the
park, then go about with a wheelbarrow and gather up the
slaughtered ones. ... At the time Col. A. A. Bird kept the
United States hotel . . . quails were known to enter the kitchen
through open windows, in their flight. One afternoon it is said
the cook captured nearly a thousand. . . (56).
Commerce
Quail were caught at Janesville during the winter of 1842-43,
showing that trapping began very early in the agricultural his¬
tory of the State (57). Roberts (58) came to Lafayette County
in 1846. He has described the use of the tunnel trap, a favorite
means of taking quail in the Mississippi Valley. This trap, popu¬
lar in Europe during mediaeval times, was doubtlessly intro¬
duced by the French colonists. When snow covered the ground,
baited traps of various types were very effective. Poor trans¬
portation facilities for a time limited the sale of quail in large
numbers for export without the commonwealth, except from the
lake ports. The accompanying map (Fig. 2) shows that rail¬
roads tapped but a small portion of the state prior to 1855. The
arrival of a railroad was followed immediately by a great in¬
crease in the traffic in quail and other game.
The first mention of a large shipment of quail is by Hoy (59) .
In the fall and winter of 1849-50, C. A. Orvis of Racine shipped
two tons of quail to the city of New York. One morning in
Schorger — The Quail in Early Wisconsin
83
Figure 2. Dates of railroad construction in Wisconsin and northern Illinois.
84 Wisconsin Academy of Sciences , Arts and Letters
November, 1852, 1,500 quail, some of them alive, were brought
to Milwaukee where they were sold at 25 cents a dozen (60).
In January of this year, 39 cents a dozen was offered at Janes¬
ville (61). Joseph Clason, of Beaver Dam, in February, 1853,
hauled to Milwaukee a load of game in which were 100 dozen
quail that had been trapped by his son (62). The traffic had
become sufficiently large that in 1852 a state law was passed
prohibiting the capture and sale of quail except from the first
Tuesday in October to February first.
The railroad from Milwaukee to Janesville was completed in
1853. The number of quail trapped and sent east from Janes¬
ville, the winter of 1853-54, was “fearful” (63). It was antici¬
pated that fewer would be trapped during the fall and winter of
1854 as the transactions had become unprofitable. Most of the
birds were taken illegally. The sellers were at the mercy of the
large buyers in the cities and were forced to take the prices
offered. Nevertheless large numbers were shipped from Janes¬
ville and Beloit. The prices, 87.5 cents to one dollar a dozen,
offered the trappers during the legal season, show a great in¬
crease. One dealer shipped 500 dozen from Beloit (64).
A Mr. Lee of Milwaukee started for New York on January
20, 1854, with 500 dozen quail. The total number shipped from
this port during the season was over 2,860 dozen (65). There
was a strong protest against trapping that was said to be done
by the “idle and vagrant.” This is not a fair statement as the
prices paid during the legal season were highly attractive to
farmers and professional trappers alike.
The exportation reached a peak in the season 1854-55. Quail
continued to arrive in Milwaukee by rail in January, and even
long after the legal season had passed. The number shipped east
was “enormous” and fears were expressed that this gamebird
would become extinct (66). In fact, it was deplored that the
traffic persisted the year round. The shipments from Beloit
amounted to 12 tons. This is equivalent to 55,000 birds as the
average weight was stated to be 7 ounces (68). A shipment of
20,000 quail from Janesville was received in Philadelphia in
January, 1856 (68a).
The Decline
The reduction in the number of quail was due to a combina¬
tion of trapping and adverse weather. The winter of 1854-55 was
Schorger—The Quail in Early Wisconsin 85
severe and this was followed by the exceptionally hard winter of
1855-56. The decline was not sudden. During the winter of
1855-56, tons of quail and other game were hanging in the yard
of the Capital House at Madison (69). However, while quail
sold for 40 cents a dozen at Lancaster, they were neither plenti¬
ful nor cheap in Milwaukee (70). In January, 1857, there was
a protest against the tons of quail that reached Milwaukee. The
market was glutted (71). A Chicago dealer, in December, 1856,
received a consignment of 214 dozen from Fond du Lac, Wis¬
consin, The high price of $2,25 a dozen, wholesale, prevailed
(72).
In the fall of 1857, compared with former years, quail were
reduced greatly in number at Janesville. (73) The sight of a
flock in the Capital Park at Madison elicited the comment that
the species was becoming quite rare in the vicinity of large
towns (74). They were unusually scarce this season in the Mil¬
waukee markets (75) .
The winter of 1857-58 was mild. In the fall of 1858, quail
were very numerous at Prairie du Chien (76). In December,
the Milwaukee market was again glutted with them. The weath¬
er at the end of this month was so unfavorable for keeping game
that quail could be purchased as low as 50 cents a dozen (77).
There were few quail at Madison (78) in the fall of 1860 in
spite of the mildness of the preceding winter. They were, how¬
ever, reported abundant at Horicon, (79) Oxford, (80) and
Burlington (81). Quail increased gradually, and were numerous
locally, until the winter of 1865-66 ; but their numbers did not
begin to compare with those for the years 1845-54. In 1861,
they were not nearly as numerous as formerly at Shullsburg.
(82) Ruffed grouse were stated to be more plentiful than quail
in 1866 in Wisconsin, though “ten years ago the quail whistled
from every fence-corner” (83).
Madison is chosen to show the rapidity of the decline. Quail
had recovered sufficiently by the fall of 1863 as to be seen almost
daily in the Capital Park (84). In 1870 it was said: “These
delicious birds, once so plentiful here, are very rarely found in
this vicinity now. We have seen none in the market this fall
until today, when Oppell had a lot of them brought from abroad.
. . .” (85). A year later the presence of a covey was an item of
note (86). For 1879, we read: “A Sun Prairie farmer tells us,
86 Wisconsin Academy of Sciences , Arts and Letters
a few days ago, he stirred up a flock of quails, thirteen in num¬
ber, and shot eight. We had thought that there was not one
quail in Dane County” (87).
During this time the quail disappeared almost completely
from the border of Lake Michigan. In the fall of 1879, a hunter
shot a quail near Milwaukee. It was the only one seen during
the season (88). They were very scarce this year also at Wau¬
kesha (89). The quail was considered a bird of the past at
Milwaukee in 1882, though a few years previously they could be
found quite plentifully two to four miles south or west of the
city (90). Willard (91), writing in 1883, had never found a
quail in Brown County; also, it was not found at this time at
Shiocton by Grundtvig (92) though he was assured by others
of its presence. Hoy (59) mentioned in 1885 that it had been
two years since he had seen a quail at Racine.
A few quail were reported present in Manitowoc County,
and also in Sheboygan County, in the fall of 1898, for the first
time in many years (93). Prior to 1868, there were hundreds of
quail in the town of Scott, Sheboygan County. None were seen
during the following 30 years. They were thought to have dis¬
appeared because a “wild bean”* upon which they fed became
scarce with settlement of the country.
The close of the century found a temporary increase in the
population, particularly in the Mississippi Valley. In 1895 there
were more quail at Eau Claire than for many years (94). They
were “abundant” in 1896 at Prairie du Chien (95), and more
numerous than usual at Trempealeau (96), Black River Falls
(97), and Stevens Point (98). Though quail had been scarce at
the latter place for years, several flocks invaded the town Oc¬
tober 9 to 12. The increase continued through 1900. They were
to be found everywhere in the country districts at Prairie du
Chien for the first time in many years (99). This year Hough
(100) found only a few quail at Waupaca but remarked that for
several years they had been moving steadily northward from
that place. In 1902, Schoenebeck (101) stated that the species
had become common in Oconto County within the past ten years.
The general statement may be made that from one decade
to another, since 1870, the quail population has remained rela¬
tively stationary.
Prof. N. C. Fassett suggested Lathyrus palustris.
87
Schorger — The Quail in Early Wisconsin
Emigration
The former periodic irruption or emigration of quail on an
extensive scale was a very interesting phenomenon. During the
movement, that took place usually in September and October,
quail entered towns, flew against houses, and crossed wide rivers.
The habit was developed to the highest degree in the North
Central states. Van Dyke (102), as late as 1891, wrote of the
quail in Minnesota: “In the early part of the fall, . . . the quail
generally have a crazy spell, during which they gather into large
flocks, travel quite a distance and even go into town and butt
their brains out against houses.”
It is not known if quail irruptions occurred under primitive
conditions. They may have taken place and yet not have been
recognized. Audubon, as is well known, observed quail cross
the Ohio River periodically during his residence in Kentucky.
One writer (103) mentions a congestion of quail, in the autumn
of 1840, on the bank of the Mississippi at Quincy, Illinois. Here
the river was approximately a mile wide. He states that the
autumnal migration, or change of quarters, was well known.
Another observer (104) mentions that at Louisville, Kentucky,
“quails migrate here from Indiana and elsewhere every three or
four years, and wherever you can And an elbow of the river, they
are very plenty, as they go to these projections to cross the river,
and many a one meets a watery grave in the attempt.” In the
fall of 1839, “some 500 or 1,000” were encountered at the junc¬
tion of the Ohio and Mississippi (105).
There is little definite information .on the extensiveness of
the emigrations or the distances travelled. In the fall of 1846,
quail emigrated in “myriads” from Iowa to Illinois, while four
years previously the movement was in the opposite direction.
Large numbers were encountered the entire distance of 30 miles
between Bloomington, Iowa, and Davenport. The observer
wrote: “We saw every hundred yards, flocks numbering from
twenty to two hundred. They seemed half deranged; they run
into town, fill the streets, and even the barns, for they break
numberless windows in their flight.” In attempting to cross the
Mississippi, a weary flock dropped upon a steamboat but “count¬
less numbers must perish” (106).
A movement of quail in 1866 across the Ohio from Indiana
to the vicinity of Louisville, Kentucky, began September 15 and
88 Wisconsin Academy of Sciences, Arts and Letters
was still in progress on October 26. It extended as far down the
river as Owensboro, so that the front of the advance was ap¬
proximately 80 miles (107). A mile seems to be about the limit
of a sustained flight. Yorke (108), on three occasions, observed
quail in flight across the Mississippi where it was at least a mile
wide. In one instance only five or six of a flock of fifteen reached
the bank.
The behaviour of quail during the fall movement has been
graphically described by a Milwaukee sportsman :
“Another western peculiarity of this bird is its annual
visit to large cities and villages in the fall. During the
fine weather of Autumn while food is in the greatest
abundance on stubble, in stack and in the high road, the
quail seeks our closely inhabited places, and may be heard
and seen all day. In the morning, he is not so often seen,
but just after noon he begins to show himself and make
himself heard. He gets on top of houses and stores, and
pipes most lustily. He drops into the smallest back yards
and gardens, piping, and rambling about as if he wished
to call your attention to him. He even parades the crowded
streets in large bevies, and actually spends the whole
afternoon loafing about the principal streets and all the
yards and gardens. . . .
“Towards sunset he becomes excited, crazy as a spec¬
ulator ... he often makes pounce at a house, hits it and
knocks himself down. . . . Even after dark he continues
this game, and you may sometimes hear him take a house
late in the evening, and you can pick him up at its base in
the morning, as dead as a herring.
“Why he does all this, we cannot say, but every boy
knows he does it, and nine-tenths of the juveniles in the
eager chase after him in the Autumn, run over your
grounds and often demolish half your garden and shrub¬
bery. Nor is this chase so unsuccessful as you might sup¬
pose. When pursued by the boys he often runs under
boards, bushes, woodpiles or rubbish, and is taken by the
hand, and often when driven by them from this covert
rushes madly against house or fence, and is taken up
dead. These vagaries are of annual occurrence, some
years the fit of insanity only lasts a few days, and some¬
times it lasts for weeks.
“Yet, while he thus visits our villages, he seems to
remain as abundant in the country. We have left a village
filled with piping quails, and yet found one or more covies
in every stubble field, and have seen them in the road
picking up the wheat dropped by the wagons.
Schorger- — The Quail in Early Wisconsin
83
“These habits he may have elsewhere, but we have
never noticed them except at the West, and know he is
not so inveterately addicted to them in the Atlantic
States, if he is at all.” (109)
About 1840, quail abounded in fall in the streets and gardens
of Chicago. Owing to their small size, they were “not much
molested by gunners” (110). In 1854 and 1855 large numbers
of quail were killed in the streets of Watertown and Madison by
boys using only sticks and stones (111). There were protests at
this time at Madison, Kenosha, and Racine against the common
practise of shooting quail in the streets (112). Sportsmen were
shooting quail on West Water Street, Milwaukee, on November
4, 1854, “something novel for a city with a population between
30 and 35,000.” (113) Nevertheless, they subsequently invaded
this city each fall from 1859 to 1862 (114). In the fall of 1863,
hundreds of quail and prairie chickens flew over or entered the
city of La Crosse (115). Quail came into the Capital Park in
the center of Madison as late as 1865 (116).
There is little doubt that the habit of quail to emigrate or
irrupt, when a certain density of population was attained, was a
powerful factor in producing the huge numbers that existed in
Wisconsin in the decade prior to 1854. A sportsman wrote from
Racine, July 18, 1849: “The winter— a real polar one — thinned
out the Quails a good deal, but still there will be abundance
according to your ideas, and if, as I expect will be the case, they
should come in the fall from the South, abundance even accord¬
ing to ours” (117) . The fall movement was clearly defined. It
is surprising to find that a spring movement took place also,
supposedly: “The quail is a permanent resident of this state,
though after the stock has been thinned off by a very severe
winter, we have known vacancies filled by emigration from the
South, both in the succeeding spring and the fall after it.” The
spring influx generally occurred, the fall always, so that it was
unnecessary to import birds after a severe winter (118) .
There is little information on how far north the large irrup¬
tions of quail extended. In the fall of 1850, hundreds of quail
arrived at Sheboygan Falls during a sleet storm, to the mystifi¬
cation of the inhabitants. They remained about the town for
months (119). The most puzzling of quail records is given by
Kneeland (120). His observations were made from August,
1856, to June, 1857, at Portage Lake, Upper Peninsula of Miehi-
90 Wisconsin Academy of Sciences , Arts and Letters
gan. A few years previously quail were unknown there but at
this time they were not uncommon on Keweenaw Point. The
quail travels largely on the ground during irruptions and it is
wholely improbable that birds from Wisconsin would cross the
wooded wilderness of the Upper Peninsula. Any quail on Kewee¬
naw Point must have been imported. Due to the heavy snowfall
characteristic of the region, the chance of their survival for a
single winter is remote.
The mass movement of quail has never had a satisfactory
explanation. The theory that the species was once migratory,
and that a vestige of the old instinct remains (121), is inade¬
quate. Wild turkeys and other animals performed similarly
without being in the strict sense migratory. It is unknown
whether a flock of quail travelled ten, a hundred, or more miles.
Recent banding studies made in Oklahoma have shown that it
is not uncommon for quail to wander in fall and winter dis¬
tances of three to 26 miles from the summer range (121a).
Without doubt the distances covered during irruptions were con¬
siderably greater. It seems that a certain density of population
stimulates an innate solicitude for adequate winter quarters and
sets the birds in motion.
Due to the invasion of towns and frequent self-destruction
against buildings, it was popularly believed that in autumn quail
became crazy and partially blind (122). Quail assemble usually
by running, less often by flying. When they were dispersed over
the streets, gardens, and buildings of a town, the structures kept
them in bewilderment. On the morning of September 7, 1855,
six members of a flock of quail flying through the village of
Whitewater failed to avoid a store and were killed (123). Muir
(124) saw quail killed by flying against his home near Kingston,
Green Lake County, when suddenly startled. Several additional
examples could be cited. Quail flush with explosive violence and
with little regard for direction. Once launched, their short wings
render them incapable of turning with sufficient rapidity to
avoid an object of unnatural dimensions.
Effect of Agriculture
There was a deep-seated tradition in the middle west that
quail were unknown to the Indians and that they were added to
the fauna by immigration or introduction. Imlay (125), for
example, wrote that quail were unknown in Kentucky when the
Schorger — The Quail in Early Wisconsin 91
first settlers arrived. He makes the fantastic statement that the
birds came over the Appalachian mountains “by following the
trail of grain which is necessarily scattered through the wilder¬
ness.”
Regarding the quail in Illinois in 1854, Kennicott (126)
makes this puzzling comment: “Very abundant throughout the
state. Introduced within twenty years.” It is difficult to believe
that he meant that the quail was not native to the state. Hub¬
bard (127) spent the winter of 1818-19 at an Indian trading-
post near modern Hennepin, Putnam County, Illinois. Quail and
prairie chickens were abundant but were not considered re¬
spectable food. By 1837, quail were being trapped by the “hun¬
dreds in a day” and sold in the city markets (128). This year
they were plentiful at Bloomington, and in 1841 sold at 25 cents
a dozen (129).
The quail was indigenous to Cook County. The following
note appeared in the Chicago Journal , September 11, 1848: “But
speaking of quails — a number of years ago, and before half the
present population of Chicago ever dreamed there was such a
place there were none of them in this region, a severe previous
winter having completely exterminated them. In view of this
. . . Gordon S. Hubbard, who was then wintering at the South,
brought up with him in the Spring a cage or box full of these
birds for breeding, and hence springs the present profusion . .
Capt. Levinge (130) shot quail near Chicago in 1838. A severe
winter like that of 1842-43 could have reduced the population
to a point where the quail would appear to be extinct. It is
hardly possible that a few imported birds could have produced
the number present by 1848.
There were no quail at Rockford, Illinois, according to
Thurston (131), when he arrived in 1837. They appeared short¬
ly after the first settlers. On the other hand, in 1833, when the
adjoining county of Stephenson was first settled, game, including
quail, was in abundance (132).
There is ample evidence that quail increased greatly simul¬
taneously with a certain stage in the development of agriculture.
Cabot (133) was told that they had increased eight-fold within
the recollection of the informer. He states : “I myself saw num¬
bers of quails in the main street [Chicago] and on the houses,
and was assured that they sometimes entered the shops. The
92 Wisconsin Academy of Sciences , Arts and Letters
cause is simply the increase of food.” The following quotation is
in a similar vein: “For twenty years after the settlement of
Northern Illinois, the deer, the grouse, and the quails increased
in numbers every year. . . . The quails were constantly on the
increase from 1840 to 1850” (134). Thurston (131) has written
that at Rockford quail were present in “countless numbers from
1844 to 1854.” Boys traded dressed quail for ammunition at a
maximum value of 18 cents a dozen. During the winter of 1852-
53, the time when the railroad reached Rockford, barrels of quail
were brought from Stephenson County for shipment east. As
will be shown later, the peak in the quail population was reached
during a series of favorable winters and it is probable that this
factor was far more important that the food supply.
When quail began to decline, the cause was attributed to
over-shooting or trapping, the state of agriculture being left out
of consideration, usually. Baldwin (135) stated that quail have
“largely decreased” since the settlement of La Salle County,
Illinois. Quail were past their peak near Fond du Lac prior to
the Civil War; yet, according to Titus (15), it was not until this
war opened that the settlers had sufficient land under cultivation
to make a “frugal but fairly comfortable living.”
Southwestern Wisconsin developed slowly in spite of early
occupation. Evans (135a) wrote: “My first impression of Platte-
ville (1846) was that of a village located in a dense forest. . . .
At this early date most of the land was uncultivated; both
prairie and timber were in primitive condition. . . . There were
few farms then; just a vast prairie between here and Shulls-
burg.” In 1854 it was said of Dane County: “. . . perhaps one-
eighth is under cultivation embracing about 1,600 farms. . . .”
(135b) The three southwestern counties, Grant, Lafayette, and
Iowa, had improved only 20 per cent of their areas by 1860.
(136) It is difficult to believe that so slight an extent of agricul¬
tural development could have affected greatly either an increase
or decline of the quail. The ratio of wild to cultivated land would
appear ideal. All stages of land improvement could be found at
this time in the southern portion of the state, yet the quail never
recovered.
It should be mentioned that the most pronounced increase in
quail took place in the prairie regions of the Upper Mississippi
Valley. Many thousands of these birds were sent to eastern mar-
Schorger — The Quail in Early Wisconsin 93
kets from Wisconsin, Illinois, and Iowa (137). Under primitive
conditions quail had great difficulty surviving a winter on the
open prairie unless the weather was exceptionally mild. It was
not, however, absent from the prairie in summer. Levinge (130),
in September, 1838, found quail in the tall grass a few miles
west of Chicago. In Wisconsin, Goss (138) found quail nesting
on the prairie miles from a tree or bush.
The quail is essentially a border bird, and as King (139) has
said occupied the ‘‘borders of groves, hazel patches and open
fields.” Even in the absence of snow the customary autumnal
burning of the prairies by the Indians deprived the birds of food
and cover over large areas. Marsh (140) mentions that in De
Kalb County, Illinois, in 1849, the quail wintered in the hazel
thickets at the edge of the woods as there was no cover beyond.
Prior to agriculture, the quail was restricted mainly to the
borders of streams and woods. A strip of hazel separated the
prairie from the timber, and whenever the latter encroached
upon the prairie, the hazel led the advance. It is evident there¬
fore that both habitat and quail population were strictly limited.
The advent of agriculture was soon followed by an apparently
optimum ratio of wild to cultivated land. Reduction of burning
permitted a rapid advance of hazel and other types of brush,
while the building of fences and the planting of hedges in¬
creased greatly the protective cover. Cultivation produced grain
and weed seeds, which in combination with cover, permitted the
quail to take over lands that were formerly uninhabitable the
year round.
Introductions
It was thought unnecessary, in 1856, to introduce quail since
winter losses were repaired by immigration from the south.
(109) It is said that quail were introduced into Minnesota in
1845 (141), but no early plantings seem to have been made in
Wisconsin. There were occasional attempts to care for the birds
during the winter (142) .
Some Tennessee quail released at Ripon froze to death during
the winter of 1884-85 (143). In 1886, birds imported from
Texas were liberated at Oskosh (144). Their subsequent his¬
tory is unknown. About 20 pairs were freed at Whitewater in
the spring of 1890 (145).
94 Wisconsin Academy of Sciences, Arts and Letters
The almost complete disappearance of the species along Lake
Michigan led to numerous attempts at reestablishment. Some
quail imported from New Orleans were released at Racine in
the spring of 1887 (146). A few birds were introduced at Ply¬
mouth about 1892 (147). Seven dozen Kansas quail were liber¬
ated at Sheboygan in 1892, but the expected increase did not
take place (148). Two Rivers was quite persistent in its efforts.
A private attempt was made in 1894 to raise birds from Texas
stock. The local gun club liberated 120 birds from Kansas in the
spring of 1895, and several hundred were released in 1897.
(149)
Sportsmen at Sturgeon Bay, in 1899, set free 140 quail re¬
ceived from Kansas. Since further stocking was discussed the
following year, there is doubt that the birds survived (150) ;
however, in 1903, the quail were said to have multiplied rapidly.
(151) Great optimism was shown by the release of quail at
Washington Island in the spring of 1902. Their existence was in
doubt by the spring of 1904 (152).
Quail were introduced at Palmyra, Jefferson County, in
1897 (153), while hundreds were liberated at Prairie du Chien
by Col. J. T. Barnum in the years prior to 1898 (154). It is
stated that at this time Gustav Pabst released large numbers of
quail in various parts of the state (155). Southern quail, lib¬
erated near Lake Koshkonong, survived the winter contrary to
expectations (156). It is very doubtful if any of the importa¬
tions have had a perceptible influence, racially or numerically,
on the native stock.
Weather
It has been recognized for a long time that the most lethal
enemy of the quail is severe weather. Crevcoeur (157), in 1782,
mentioned a severe winter in the east that reduced the species
to near extinction. Hoy (59) wrote of a winter at Racine during
which hundreds of quail froze to death in groups of ten to fifteen
while roosting. The mortality caused by cold and deep snow is
stressed by Muir (124a). One of his neighbors was watching
some quail when 'They actually fell down and died.” Mrs. S.
Littlefield (157a) mentions a severe winter that killed quail in
Sheboygan County and that she actually saw them drop dead.
The first Wisconsin winter mentioned in connection with
quail mortality is that of 1842-43. It was long known for its low
Schorger—The Quail in Early Wisconsin
95
temperatures and deep snows. There was sleighing from the
10th of November to about the same date in April. A thaw in
January followed by rain produced a crust on the snow, making
the worst possible conditions for game birds. Quail were nearly
exterminated. A gentleman at Janesville purchased from trap¬
pers 100 quail that were liberated the following spring (57).
There followed a succession of mild winters until that of 1848-
49, giving the quail a chance to become plentiful. During the
latter winter, snow and sleet killed “thousands” in Iowa (158)
and reduced considerably the number in Wisconsin (117).
Quail had increased so rapidly in Wisconsin along the Missis¬
sippi Kiver by the spring of 1854 that they were expected to
“swarm” should the following winter be mild (159). This hope
was not realized as the winter was severe. A storm in December
drove large numbers into the settlements around Jefferson (160)
where they were trapped easily.
The winter of 1855-56 was very severe throughout the north¬
ern and eastern states. The deep snow by December had driven
the quail into the farmyards. They were numerous at Kilbourn
(Wisconsin Dells) until the cold weather of January, 1856, when
they disappeared (161). A letter from Belvidere, Boone County,
Illinois, states that few quail lived through the winter. There
was a better survival, supposedly, in Wisconsin “on account of
having woods for shelter” but that even there quail were few in
comparison with other years (162). They were said to have
been nearly exterminated in Grant County and that it was many
years before they were numerous again (163).
The belief persisted that a warm winter would restore the
population. One writer states that though the winters of 1854-55
and 1855-56 “have thinned his numbers deplorably, but a single
warm winter will bring him to us in abundance, and a couple of
them in extra abundance. . . .” (109). Unfortunately the winter
of 1856-57 was also severe on quail (164), so that there were
three successive killing winters. The "winter of 1857-58 was mild
and to it was attributed the presence of numerous quail at
Prairie du Chien in the fall of 1858 (165) . It was not considered
good sportsmanship to shoot quail until the autumn of 1859
since until that time they had not become sufficiently plentiful.
(166)
The nature of the southern Wisconsin winters from 1840 to
96
Wisconsin Academy of Sciences , Arts and Letters
1900 is described in general terms in Table I. A detailed analysis
of each winter would extend this paper to unjustifiable length.
The statement, “quail killed,” has been used only when it is
supported by literature references for the particular winter.
The factors governing winter survival are varied and complex.
Quail that are well fed have an excellent chance of living
through the winter (167), but during rigorous weather birds in
seemingly good condition may perish (168). When the body
weight drops below 70 per cent of normal, through cold or lack
of food, quail are particularly vulnerable to subzero tempera¬
tures. February and March are usually the critical months. A
covey that survives in weakened condition until March may be
exterminated by a single snowstorm, while a drifting snow that
becomes crusted may be fatal at any time.
It is easy to understand why some of the earliest settlers
reported quail absent or scarce when it is realized that poten¬
tially 1833-34, 1834-35, and 1837-38 were killing winters. Each
of these winters had one month during which the mean tempera¬
ture was 9 or 10 degrees. There was an insufficiently long run
of favorable weather to permit a large increase in the popula¬
tion. Beginning with the winter of 1843-44 and extending
through that of 1853-54, a period of 11 years, there was a re¬
markable succession of mild winters, the only interruption being
that of 1848-49. This series of mild winters has never been
duplicated. It is evident why the peak in population was possible
in 1854.
Table I. Character of Southern Wisconsin Winters, 1840-1900
1840- 41 Mild
1841- 42 Very mild.
1842- 43 Very severe. Deep snow with crust. Quail killed.
1843- 44 Mild.
1844- 45 Very mild.
1845- 46 Mild.
1848-47 Comparatively mild. Deep snow.
1847- 48 Exceptionally mild. Little snow.
1848- 49 Severe. Deep snow and ice. Quail killed.
1849- 50 Mild. Little snow.
1850- 51 Mild. “Moderate open winter.”
1851- 52 Comparatively mild. Heavy snow in March melted rapidly.
1852- 53 Mild. Little snow. “An open winter.”
1853- 54 Comparatively severe. Cold with deep snow the end of January.
February mild.
1854- 55 Severe. Quail killed.
1855- 56 Very severe. Quail killed.
1856- 57 Severe. Quail killed.
1857- 58 Mild.
Schorger — The Quail in Early Wisconsin
97
1858- 59 Mild.
1859- 60 Mild. “Open.”
1880-61 Comparatively severe. Deep, drifted snows in January.
1861- 62 Severe. Exceptionally heavy snow fall.
1862- 63 Very mild.
1863- 64 Severe. Heavy snow.
1864- 65 Severe.
1865- 66 Severe. Rain, cold, drifted snow.
1866- 67 Mild.
1867- 68 Severe, “Steady cold.”
1868- 69 Comparatively severe. Deep snow.
1869- 70 Exceptionally mild.
1870- 71 Mild.
1871- 72 Comparatively severe. Numerous snowstorms.
1872- 73 Very severe. “Hardest on record.” Quail killed.
1873- 74 Comparatively severe. Deep snows.
1874- 75 Very severe. Quail killed.
1875- 76 Very mild.
1876- 77 Comparatively severe. Cold with deep, drifted snow in January.
1877- 78 Very mild. “Open winter.”
1878- 79 Comparatively mild. Low temperatures in January.
1879- 80 Very mild. ‘‘Exceptionally fine.”
1880- 81 Severe. Exceptionally heavy snowfall. Blizzards. Quail killed.
1881- 82 Very mild.
1882- 83 Severe. Extreme cold and deep, crusted snow. Quail killed.
1883- 84 Severe. Quail killed.
1884- 85 Very severe. Very cold in January and February. Quail killed.
1885- 86 Severe.
1886- 87 Very severe. Blizzards.
1887- 88 Severe. Drifted and crusted snow.
1888- 89 Mild. “One of the mildest on record.”
1889- 90 Very mild.
1890- 91 Mild.
1891- 92 Comparatively mild.
1892- 93 Very severe.
1893- 94 Mild.
1894- 95 Severe.
1895- 96 Mild.
1896- 97 Mild.
1897- 98 Mild.
1898- 99 Comparatively severe. Quail killed.
1899- 00 Mild.
The question may be raised whether food or weather was
the more important factor in producing the peak in population
in 1854 and the subsequent decline. The commerce in quail that
became extensive about 1852, and was pursued vigorously for
many years, was contributory to the decline, especially since
quail could be trapped so easily in severe weather. It is reason¬
ably clear, however, that weather played the important role.
The birds, after the series of three severe winters beginning
with 1854-55, never again approached their former numbers.
Food must have been as ample as formerly during the three mild
winters starting with 1857-58, but the population was so de¬
pleted that there was only a limited recovery. Similar series of
98 Wisconsin Academy of Sciences , Arts and Letters
three favorable winters occurred only three additional times be¬
fore the end of the century. When there was a succession of six
hard winters such as that between 1882-83 and 1887-88, it is
surprising that the species survived.
It is stated by Gerstell (170) that the quail stands near the
bottom of the list of gamebirds in its ability to withstand lack
of food; and that even under favorable food conditions there is
a high mortality due to environmental extremes. Artificially
propagated quail, confined individually without food, showed the
following survival time : 1.9 days at 0° F. with an air movement
of 5.8 miles per hour ; and 2.5 days at the same temperature with
no movement of the air. Due to conservation of heat, the chances
of survival in a bevy are increased greatly. A group of 10 birds,
owing to the opportunity to huddle closely while roosting,
showed an average survival of 4.1 days at 0° F. and no air move¬
ment.
Quail roost usually upon the ground in a compact circle.
There are exceptions. The following note was made at Madison,
March 23, 1930: “About 6 inches of snow fell last night. . . .
At 2 :45 found 5 quail (there might have been more) roosting in
a clump of spruce trees near the old sand pit. They were about
15 feet from the ground. About 200 yards up the same road,
found 8 quail roosting in a grapevine tangle about 12 feet from
the ground. This roost was quite open but offered good pro¬
tection against large owls.” I have never, however, found an
elevated roost during severe weather.
The argument that quail, after attaining a certain abun¬
dance, may as well be shot, since they are sure to approach
extermination during the next cold winter, is an old one in Wis¬
consin (168). While there is some truth in this assertion, it
produces a dilemma. The normal bevy of 15 to 20 birds has the
best chance of survival. If it is reduced to 4 or 5 birds prior to a
hard winter, the chance of the remnant surviving is much more
remote. It is improbable that many of the reduced coveys would
combine for the winter since in most regions the coveys are too
widely separated.
There is no prospect that quail will become numerous in Wis¬
consin in the near future. The effects of weather are largely
beyond management. Cover continues to deteriorate. Where it
is not removed deliberately, its effectiveness is reduced greatly
Schorger—The Quail in Early Wisconsin
99
by grazing. Dairying and the raising .of stock are injurious to
both cover and the food supply. It is evident, therefore, that the
improvement of present conditions for quail are for the most
part not subject to control.
Addenda
Editor D. J. Powers ( Wisconsin Farmer 9, 1857, p.231)
states that approximately 25,000 quail were sent from Madison
to Chicago the winter of 1855-56. He thinks that an estimate of
500,000 quail sent to eastern cities from Milwaukee and Chicago
would be low.
Howard Bosworth ( Forest and Stream 56, April 13, 1901,
p.287) knew of one or two places in the valley of the Wisconsin
River where he could have killed 75 quail a day in the fall of
1901.
Quail were first observed at Schilling Station. Clark County,
in the fall of 1901 (Greenwood Gleaner Oct. 18, 1901).
A. H. Pape liberated quail in 1899 in Waupaca County (New
London Republican Sept. 22, 1903), and in the spring of 1903
a few were set free in Burnett County (Grantsburg Sentinel
Nov. 12, 1903).
Literature Cited
1. A. N. Somers, Pop. Science Monthly 42 (1892) 203.
2. T. Rodolf, Wis. Hist. Coll. 15 (1900) 345.
3. C. Rodolf. In: History of Grant County, Wisconsin. Chicago, (1881)
p. 800.
4. Gen. William R. Smith. Observations on the Wisconsin Territory. Phil¬
adelphia, (1838) p. 24.
5. G. W. Featherstonhaugh. A canoe voyage up the Minnay Sotor. London.
Vol. 1 (1847) p. 180.
5a. “The Upper Wolf, Wis.” Vol. 6, No. 8, Wisconsin Local History. Wis.
Hist. Soc.
5b. Watertown Chronicle Nov. 3, 1847.
6. Mrs. Mary Bristol, Wis. Hist. Coll. 8 (1879) 303; 15 (1900) 238.
6a. H. Pratten. In: D. D. Owen, Report of a geological survey of Wisconsin,
Iowa, and Minnesota. Philadelphia, (1852) p. 623.
7. E. W. Keyes, Wis. Hist. Coll. 11 (1888) 424.
8. Prosper Cravath. Early annals of Whitewater. Whitewater, (1908) p. 40;
cj. Whitewater Register Sept. 11, 1858.
8a. Ibid., p. 178.
9. Whitewater Register Nov. 13, 1858.
10. Anon. Life in the west. London, (1842) p. 275.
11. I. A. Lapham. A geographical and topographical description of Wiscon¬
sin. Milwaukee, (1844) p. 76.
100 Wisconsin Academy of Sciences, Arts and Letters
12. H. A. Tenney. In: D. S. Durrie, History of Madison. Madison, (1874)
p. 163.
13. Martin Mitchel. History of the county of Fond du Lac. (1854) p. 80.
14. Capt. L. B. Mackinnon. Atlantic and transatlantic: sketches. N. Y.
(1852) p. 136.
15. W. A. Titus, Wis. Mag. Hist. 19 (1936) 415.
15a. C. T. Ficker, ibid., 25 (1942) 349.
16. J. V. Quarles, ibid., 16 (1933) 297-320.
17. Mrs. L. T. Fowler, ibid., 18 (1935) 397.
18. F. S. Stone. History of Racine County. Chicago. Vol. 1 (1916) p. 421.
19. W. H. M. A reminiscence. Burlington Free Press Sept. 26, 1882.
19a. Silas Chapman. Early Waukesha days. Waukesha Freeman July 10,
1890 [1].
20. James L. Breck. Life. New York, (1883) p. 60.
21. Milwaukee Sentinel Aug. 17 and Oct. 7, 1846.
22. D. McLeod. History of Wiskonsan. Buffalo, (1846) p. 238.
23. Madison Argus Aug. 3, 1847.
24. Watertown Chronicle Aug. 18, 1847.
25. A. S. H. Porter's Spirit of the Times, 17 (Sept. 11, 1847 ) 333.
26. Milwaukee (w) Wisconsin Aug. 18, 1847.
27. Jacob Biihler, Wis. Mag. Hist. 16 (1923) 325.
28. A. C. Barry, Proc. Boston Soc. Nat. Hist. 5 (1854) 8.
29. Hudson North Star July 4 and Aug. 8, 1855.
30. Wausau Pilot Nov. 14, 1868.
31. Ashland Press Sept. 26, 1874.
32. Superior Times July 29, 1882.
33. Florence Mining News Nov. 21, 1891.
34. Madison (w) Argus and Democrat Dec. 7, 1852.
35. Prairie du Chien Courier Oct. 20, 1852.
35a. J Q. Emery. Early history of Rutland. Madison Democrat April 18, 1920.
36. P. R. Hoy, Trans. Wis. Agr. Soc. for 1852, (1853) 357.
37. Wisconsin State Journal Oct. 8, 1853.
38. Appleton Crescent Oct. 22, 1853.
39. Porter’s Spirit of the Times, 22 (Jan. 22, 1853) 583.
40. Waukesha Press. In: Juneau Gazette July 29, 1853.
41. Janesville Democratic Standard Aug. 9, 1854; Madison Argus and Demo¬
crat Dec. 29, 1854.
42. Watertown Chronicle. In: Madison Argus and Democrat Oct. 19. 1854.
43. Jefferson Jeffersonian. In: Ibid., Nov. 6, 1854.
44. ‘‘Badger,” Porter’s Spirit of the Times 24 (Nov. 18, 1854) 476.
45. Green Bay Advocate March 23; Nov. 16, 1854.
46. Milwaukee (d) Wisconsin Jan. 31, 1855.
47. Ibid., Aug. 25, 1855; Milwaukee American Oct. 17, 1855.
48. Elkhom Reporter. In: Milwaukee (d) Wisconsin July 18, 1855.
49. Waukesha Plain Dealer Oct. 16, 1855.
50. Watertown Democrat Jan. 4; Aug. 30, 1855.
51. Madison (d) Argus and Democrat Oct. 29, 1855.
52. Jefferson Republican. In: Madison (d) Patriot Dec. 8, 1855.
53. Portage Badger State Jan. 4, 1856.
Schorger — The Quail in Early Wisconsin
101
54. Milwaukee (d) News Sept. 7, 1856.
55. Ibid., Sept. 14, 1856.
56. Madison Democrat Dec. 23, 1881.
57. Portage Badger State Dec. 26, 1856; Madison State Journal Dec. 27, 1856.
58. S. E. Roberts, Darlington Democrat March 27, 1919.
59. P. R. Hoy, Proc. Wis. Nat. Hist. Soc. March, 1885, p. 8.
60. Milwaukee Sentinel Nov. 26, 1852.
61. Janesville Democratic Standard Jan. 21, 1852.
62. Milwaukee Sentinel Feb. 2, 1853.
63. Janesville Democratic Standard Feb. 1; Aug. 9, 1854.
64. Madison Argus and Democrat Dec. 29, 1854.
65. Milwaukee Sentinel Jan. 21 and 31, 1854.
66. Ibid., Jan. 20, 1855.
67. Ibid., Feb. 20, 1855; Whitewater Gazette Feb. 7, 1856.
68. Beloit Journal. In: Milwaukee Sentinel Feb. 10, 1855.
68a. E. J. Lewis. American Sportsman. Philadelphia, (1863) p. 64.
69. Milwaukee (d) News June 10, 1856.
70. Milwaukee Sentinel Jan. 10; Feb. 7, 1856.
71. Milwaukee (w) Wisconsin Jan. 28, 1857.
72. Chicago Tribune Dec. 20, 1856; Milwaukee Sentinel Dec. 22, 1856.
73. Janesville Gazette Aug. 10, 1857.
74. Madison (d) Patriot Sept. 29, 1857.
75. Milwaukee Sentinel Jan. 4, 1858.
76. Prairie du Chien Courier Sept. 16, 1858.
77. Milwaukee Sentinel Dec. 28, 30, and 31, 1858.
78. Madison (d) Argus and Democrat Oct. 12, 1860.
79. Horicon Argus Sept. 21; Oct. 19; Nov. 16, 1860.
80. Oxford Express Aug. 31, 1860.
81. Burlington Gazette Aug. 14, 1860.
82. Shullsburg Local Sept. 6, 1861.
83. “Snap Shot,” Wilkes’ Spirit of the Times 15 (Oct. 20, 1866) 129-30.
84. Madison State Journal Sept. 25, 1863.
85. Ibid., Dec. 8, 1870.
86. Madison Democrat Nov. 1, 1871.
87. Ibid., Dec. 30, 1879.
88. L’Eclair, Forest and Stream 13 (1879) 714.
89. H. W. Merrill, ibid 13 (1879) 827.
90. “Blue Jay,” Am. Field 17 (June 24, 1882) 440.
91. S. W. Willard, Wis. Acad. Sci. 6 (1885) 189.
92. F. L. Grundtvig, ibid., 10 (1895) 105.
93. Manitowoc Pilot Aug. 25, 1898; Plymouth Review March 6; May 22; Dec-
25, 1901.
94. Eau Claire Telegram Aug. 4, 1895, 1.
95. Prairie du Chien Courier Nov. 10, 1896.
96. Trempealeau Herald Aug. 28, 1896.
97. Black River Falls Journal Aug. 27 and Banner Oct. 8, 1896.
98. Stevens Point Gazette Oct. 14, 1896, 4, and Journal Oct. 17, 1896. 8.
99. Prairie du Chien Courier Oct. 23, 1900.
100. E. Hough, Forest and Stream 55 (Oct. 6, 1900) 268.
102 Wisconsin Academy of Sciences , Arts and Letters
101. A. J. Schoenebeck. Birds of Oconto County. [1902], p. 21.
102. T. S. Van Dyke. Bob-White in Minnesota. Shooting and Fishing 10,
No. 7 (June 11, 1891) 11-13.
103. H. M., Porter's Spirit of the Times 11, No. 8 (April 24, 1841) 90.
104. G. ibid., 11 (March 13, 1841) 19.
105. N. ibid., p. 25.
106. J. G., ibid., 16 (Oct. 24, 1846) 415.
107. “Bang,” Turf, Field and Farm 3 (Nov. 10, 1866) 295.
108. F. H. Yorke, Am. Field 32 (Dec. 14, 1889) 553.
109. Milwaukee (d) News Nov. 16, 1856.
110. S. C. C., Wildwood's Magazine 2 (1889) 98.
111. Madison Argus and Democrat Oct. ly, 1854 and (d) Patriot Oct. 12, 1855.
112. Madison (d) Patriot Nov. 21, 1854; Kenosha Telegraph Oct. 25, 1850;
Racine Advocate Oct. 14, 1853 and Oct. 16, 1854.
113. Milwaukee (w) Wisconsin Nov. 8, 1854.
114. Milwaukee Sentinel Oct. 14 and 15, 1859; Milwaukee (d) Wisconsin Oct.
17, 1860; Sentinel Sept. 19, 1861 and Oct. 10, 1862.
115. La Crosse (w) Democrat Oct. 10, 1863.
116. Madison Democrat Oct. 12 and 19, 1865.
117. B. and S. Sporting in Wisconsin. Porter's Spirit of the Times 19 (Aug. 31,
1849) 295.
118. Milwaukee (d) News Nov. 9 and 16, 1856.
119. Anon. Quail or bob -white. Sheboygan Falls News April 6, 1892.
120. S. Kneeland. Proc. Boston Soc. Nat. Hist. 6 (1859) 237.
121. E. Sandys and T. S. Van Dyke. Upland game birds. London, (1904)
p. 25.
121a. L. G. Duck, J. Wildlife Management 7 (1943) 367.
122. Anon. Racine, Wis. Porter's Spirit of the Times 24 (Oct. 28, 1854) 436.
123. Milwaukee (d) Democrat Sept. 19, 1855.
124. J. Muir. The story of my boyhood and youth. N. Y. (1913) p. 133.
124a. Ibid. pp. 134 and 152.
125. G. Imlay. A topographical description of the western territory of North
America. 2nd. ed. London, (1793) p. 101.
126. R. Kennicott, Trans. 111. State Agr. Soc. for 1853-54, 1 (1855) 586.
127. G. S. Hubbard. Autobiography. Chicago, (1911) p. 63.
128. Illinois in 1837. Philadelphia, (1837) p. 41.
129. E. Duis. The good old-times in McClean County, Illinois. Bloomington,
(1874) pp. 311 and 342.
130. R. G. A. Levinge. Echoes from the backwoods. London. Vol. 2 (1846)
p. 215.
131. J. H. Thurston. Reminiscences, sporting and otherwise of early days in
Rockford, Ill. Rockford, (1891) pp. 104 and 111.
132. A. L. Ful wider. History of Stephenson County, Illinois. Chicago. Vol. 1
(1910) p. 146.
133. J. E. Cabot. In: L. Agassiz. Lake Superior. Boston, (1850) p. 68.
134. C. Game in the west. Wilkes’ Spirit of the Times 17 (Dec. 28, 1887) 334.
135. E. Baldwin. History of La Salle County, Illinois. Chicago, (1877) p. 529.
135a. J. H. Evans, Proc. Wis. Hist. Soc. ior 1909, (1910) pp. 234 and 237.
135b. Madison State Journal June 6, 1854.
Schorger — The Quail in Early Wisconsin
103
136. J. Schafer. Wisconsin lead region. Madison, (1932) p. 162.
137. T. F. DeVoe. The market assistant. N. Y. (167) p. 164; Milwaukee (d)
Wisconsin Nov. 28, 1855, [2].
138. B. F. Goss. In: C. Bendire. Life histories of North America birds.
Washington. Vol. 1 (1892) p. 3.
139. F. H- King. Geology of Wisconsin. Vol. 1 (1883) p. 457.
140. C. W. Marsh. Recollections 1837-1910. Chicago, (1910) p. 41.
141. Milwaukee Sentinel March 18, 1869, [2].
142. Madison State Journal Dec. 27, 1856; Palmyra Enterprise Jan. 23, 1878.
143. Milwaukee Journal Feb. 7, 1885, [2].
144. Ibid., Nov. 1, 1886.
145. Whitewater Register April 24; Sept. 4, 1890.
146. Racine Times March 11, 1887.
147. Plymouth Review July 1, 1903.
148. Sheboygan Telegram March 22, 1892; Plymouth Review Dec. 2, 1903.
149. Two Rivers Chronicle Feb. 27, 1894; Feb. 2 and 20, 1897; Kewaunee
Enterprise Jan. 22, 1897.
150. Sturgeon Bay Democrat April 14, 21 and Aug. 25, 1899; cf. Jan. 20, 1899;
Jan. 13, 1900.
151. Sturgeon Bay Advocate Jan. 18, 1902; Feb. 7, 1903; Democrat Oct. 31,
1903.
152. Sturgeon Bay Democrat Aug. 23, 1902: Advocate March 12, 1904.
153. Palmyra. Viroqua Censor Sept. 22, 1897, [4],
154. Prairie du Chien Courier Sept. 6, 1898.
155. Plymouth Review Aug. 14, 1901, [4],
156. L. Kumlien and N. Hollister. Birds of Wisconsin. (1903) p. 55.
157. J. H. St. John [De Crevcoeur], Letters from an American farmer.
London, (1782) p. 30.
157a. Plymouth Review Dec. 25, 1901.
158. ‘‘Short Pete,” Porter’s Spirit of the Times 19 (April 14, 1849) 90.
159. “H. of Wis. ,” ibid., 24 (May 27, 1854) 176.
160. Jefferson Jeffersonian. In: Milwaukee (d) Democrat Dec. 21, 1854.
161. Kilbourn Mirror Jan. 22, 1856.
162. “Don,” Porter’s Spirit of the Times, n.s. 1 (Dec. 27, 1856) 269.
163. History of Grant County, Wisconsin. Chicago, (1881) p. 473.
164. Janesville Gazette Aug. 10, 1857.
165. Prairie du Chien Courier Sent. 16, 1858.
166. Milwaukee News Sent. 16, 1859, \2l.
167. P. L. Errington. The wintering of the Wisconsin bob-white. Trans.
Wis. Acad. Sci. 28 (1933) 1-35.
168. A. Leopold, Am. Mid. Naturalist 18 (1937) 408-416; P. L. Errington,
Wilson Bull 51 (1939) 22-37.
169. E. Miller. A century of temperatures in Wisconsin. Trans. Wis. Acad.
Sci. 23 (1927) 169.
170. R. Gerstell. The place of w'nter feeding in nractical wildlife manage¬
ment. Research Bull. No. 3, Pa. Game Com., Harrisburg (1942).
171. Milwaukee Sentinel Feb. 18, 1903.
SMALL MAMMAL CENSUSES NEAR PRAIRIE DU SAC,
WISCONSIN
Harold C. Hanson
Research Assistant* Department of Wildlife Management
University of Wisconsin
Introduction
Each winter since 1930 the gamebirds and predators on a
seven square mile area in Westpoint Township, Columbia Coun¬
ty near Prairie du Sac have been censused. The results of these
censuses will be summarized in a forthcoming paper by Erring-
ton. In order to fill the gaps in our knowledge concerning the
populations of animals not heretofore censused, the writer, dur¬
ing the years 1941 and 1942, made censuses of mice and shrews,
cottontail rabbits, fox and gray squirrels, winter birds, and
nesting songbirds. This paper summarizes the data obtained on
populations of mice, shrews, and cottontail rabbits. It also in¬
cludes notes on four little-known Wisconsin mammals: pygmy
short-tailed shrew ( Cryptotis parva parva) , least weasel ( Mus -
tella rixosa allegheniensis) , harvest mouse ( Reithrodontomys
megalotis pectoralis) , and the pine mouse ( Pitymys pinetorum
scalopsoides) .
Fifteen quadrats in 12 cover types were censused between
September 21 and October 29, 1941 : Grain stubble (two fields) ;
Alfalfa (two fields) ; Bluegrass— sweet clover two fields) ; Car ex
stricta bog; Smartweed — foxtail; Short-grass prairie relic;
Sandy field (primarily panic grass) ; Juniper bluff ; Red oak and
red cedar pasture ; Whitebirch — prickly ash ; Red and white oak
woodlot (severely grazed) ; Red and white oak woodlot (moder¬
ately grazed).
Materials and Method
Quadrats employing snap traps have been used by a number
of authors (Bole 1939, Townsend 1935, Williams 1936). Live
trapping and banding have been used with notable success by
* Now Assistant Game Technician, Illinois Natural History Survey, Urbana, Illinois.
105
106 Wisconsin Academy of Sciences , Arts and Letters
Burt (1940) and Blair (1940 a, b, c) while censuses by means
of nest boxes have yielded much information not obtainable by
either of the other two methods (Nicholson 1941).
Because of the large number of cover types that had to be
sampled in a brief period, it was decided that quadrat trapping
with snap traps would be most suitable. That snap traps when
properly employed can obtain adequate estimates of small mam¬
mal populations has been shown by Goodnight and Koestner
(1942), who made a field comparison between live traps and
snap traps, and found that the two techniques were of about
equal value. They found that snap traps gave the approximate
total population in three days, while live traps took two or three
days longer.
Previous investigators (see Burt 1940, 36-39) have estimated
small mammal populations on the basis of the catches they ob¬
tained from quadrats only a fraction of the size of the home
range of any one individual.
In this work, unless otherwise specified, quadrats 300 feet
square containing 121 traps spaced ten yards apart were used.
Each quadrat was trapped for four nights. This is a modifica¬
tion of the method used by Burt (op. cit. 12-14). He found that
quadrats from two to five acres, containing live traps similarly
spaced, usually caught most of the shrews and mice in four suc¬
cessive nights of trapping.
Before cool weather set in, crickets proved to be very
troublesome in eating the bait, which consisted at first of a mix¬
ture of rolled oats and peanut butter. By experimentation it was
found that a moist crumbly mixture of millet, rolled oats, and
peanut butter was better because the millet withstood the depre¬
dations of the crickets, and thus remained available to the mice.
Regardless of the size of quadrat used, small mammals whose
home ranges border the quadrat area are likely to be taken
(Dice 1941). Some adjustment must be made for catches of
these bordering individuals when calculating density. The au¬
thor believes the most equitable method of determining the cov¬
erage of snap trap quadrats is that suggested by Dice (1938) ;
that is, to consider the area censused to be the area of the quad¬
rat itself, plus an additional distance beyond its periphery equal
to the radius of the home range of the species in question. In
Hanson — Small Mammal Censuses
107
this paper each quadrat is assumed to have drawn upon peri¬
pheral zones as follows :
These censuses are first discussed quadrat by quadrat. A
later discussion deduces habitat preferences for each species.
Additional notes on individual species are included in the latter
section.
A few quadrats were inhabited by both species of Peromy-
scus. Because these mice are difficult to separate before adult¬
hood, the identifications are doubtful for a few of the immatures
taken.
Calculations of the number of mice per acre usually produced
decimal figures. When these involved only a fraction of a mouse
per acre, they can not be rounded off without distorting the
species ratio. Hence, all densities have been left in decimals, but
it should be understood that this does not imply accuracy to one
decimal.
Status of the Rodent Cycle in 1941
Mice were generally abundant in all habitats censused in the
fall of 1941. During the fall of 1942, according to a farmer on
the Prairie du Sac area, mice were far more numerous in his
fields than during the previous year. Field experience by the
author and other Wisconsin workers leaves little doubt that the
small rodent population “crashed” some time between late in
the winter of 1942-48 and early spring. Repeated trapping dur¬
ing that spring and summer in hayfields, bluegrass areas, sand
prairies, and waste places yielded but a few specimens. However,
Peromyscus leucopus was found in fair numbers in a wooded
ravine in the Baraboo hills. This leads the author to suspect that
this species may not be cyclic, or if it is cyclic, that its numbers
do not fluctuate as violently as field-inhabiting species.
108 Wisconsin Academy of Sciences , Arts and Letters
Cover Types and Populations
Grain Stubble
Two grain stubble-fields were censused. The catch taken
from the two fields reflected the character and density of the
cover ; Field I having sparse stubble and a poor growth of weeds,
had a population of only 1.7 mice per acre, while Field II, having
a fertile black soil which supported a dense growth of weeds,
yielded 5.2 mice per acre. Table I suggests that as grain stubble-
fields became increasingly weedy, there is a corresponding in¬
crease in the rodent population, particularly of the genus, Micro-
tus. Thus besides reducing crop yields through competition,
wreeds may also be the indirect cause of crop losses because of
the high rodent populations they seem to encourage.
Table I. Number of mammals caught, calculated density per acre, and compo¬
sition of population of two grain stubble-fields, September 21-28, 1941.
Bluegrass — Sweet Clover
The quadrat used in Field I was 300 feet square, while Field
II with an area of 4.25 acres was trapped in its entirety. Since
the latter field was bordered by woods on three and one-half
sides, it was possible to trap it to exhaustion before an influx
of mice through the one opening to an adjoining field could seri¬
ously affect the catch. During the four census nights, eighty
mice were caught and in the following three nights only an addi¬
tional fifteen mice were secured. However, to make the census
figures for all cover types comparable, the population figures
Hanson— Small Mammal Censuses
109
given in Table II are based on the standard four-night trapping
period.
There was a greater proportion of bluegrass and a more
luxurious growth of weeds in Field II, thus accounting for the
proportionately greater catch of field voles, Microtus ochrogas-
ter , which reach their highest populations in dense cover. A cor¬
respondingly lower population of prairie deer mice (Peromyscus
maniculatus) also reflects this cover difference, as they are
known to prefer habitats having a more open ground surface.
Woodland deer mice are computed as a part of the total field
inhabiting population, since it was evident that portions of the
fields bordering the woods were important parts of their home
ranges.
Table II. Number of mammals caught, calculated density per acre, and com¬
position of population of two fields of bluegrass and sweet clover,
Oct. 2-11, 1941.
Alfalfa
Field I was censused with a quadrat 300 by 300 feet and Field
II with a quadrat 300 by 240 feet. The census figures for these
two fields in Table III suggest that an average alfalfa field sup¬
ported seven to eight mice per acre in the fall of 1941. Again it
is evident from a comparison of the rodent populations for Fields
I and II (Table III) that a field supporting a fairly high Micro¬
tus population is generally inhabited by a correspondingly lower
prairie deer mouse ( Peromyscus maniculatus bairdi) population.
110 Wisconsin Academy of Sciences , Arts and Letters
Table III. Number of mammals caught, calculated density per acre, and com¬
position of population of two alfalfa fields, September 23 — Oct. 5, 1941.
Car ex stHcta Bog
The total small mammal population of this bog (Table IV)
compares very closely with that obtained for alfalfa fields. Its
population was characterized by relatively low populations of
non-microtine species and the presence of a shrew, which species,
like voles, were found to be most abundant in dense cover.
The entire bog of 1.5 acres was trapped.
Table IV. Number of mammals caught, calculated density per acre, and
composition of population of a Carex stricta bog, October 16-19, 1941.
Smartweed — Foxtail
This habitat occupied a small basin at the foot of a steep dry
hill (populations on this hill are discussed under Prairie Relic)
and was censused in its entirety as it had an area of only 2.1
acres. Due to the fact that this site was inadequately tiled,
Hanson — Small Mammal Censuses
111
drainage from the surrounding fields often made it too wet to
cultivate in the spring. The central portion had been ploughed
the previous spring, but had to be abandoned, and a dense
growth of yellow foxtail and ragweed marked this sector at the
time of the census. Beggar’s tick (Bidens) and smartweed
(Polygonum) were the most abundant plants. Newly planted
timothy, a mature stand of alfalfa, and a cornfield adjoined three
sides of the basin while on the fourth side northeast it merged
with the Carex stricta bog previously discussed.
During the census period, October 16-19, the nearby corn¬
field was cut and shocked, which may have increased the catch.
The catch of house mice was so spectacular (see Table V) that
I believe it to be unlikely that this disturbance affected the
results to any great degree.
House mice were so abundant in this 2.1 acre plot it seemed
improbable that four nights of trapping could have completely
exhausted the resident population. To test this possibility a fifth
night of trapping was carried out and eleven more house mice,
three voles, two prairie deer mice, and a harvest mouse were
caught.
The top-heavy population of house mice in this habitat is a
striking illustration of how “animal weeds” may overrun the
land side by side with plant weeds. Undoubtedly the magnet
which attracted the high rodent population was the abundant
food supply, the ground being thickly strewn with seeds of fox¬
tail grass, ragweed, and smartweed. In contrast to this situa¬
tion was the “hostility” of the relatively undisturbed adjoining
Carex stricta bog. In spite of the extreme density of house mice
on this quadrat none were taken in the central portion of the
bog (Table IV).
Table V. Number of mammals caught, calculated density per acre, and
composition of population of a smartweed — foxtail habitat,
October 16-19, 1941.
112 Wisconsin Academy of Sciences , Arts and Letters
Short-grass Prairie Relic
Many areas like this one are found in southwestern Wiscon¬
sin on steep westerly-facing hillsides. The five domiant plants
composing this relic were: Andropogon scoparius Sporobolus
heterolepis, Aristida basiramea, Amorpha canescens , and Aster
sericeus . Because of the topography, it was necessary to lay
out the traps in the form of a triangle that spread down fan-
wise from the peak of the hill. Consequently there was a rela¬
tively large amount of edge across which mice from the different
surrounding cover types might have drifted. For this reason the
census figures in Table VI are not strictly comparable with those
given for the other types. The area covered by the traps was 0.8
acre but the actual coverage was assumed to be one acre.
As might be expected the prairie deer mouse ( Peromyscus
maniculatus) was the dominant species in this relic. The wood¬
land deer mice ( Peromyscus leucopus) were taken from amongst
a thicket of wild grape and bittersweet on an outcropping of
limestone in the center of the census area. The genus Microtus
was conspicuously absent, possibly because the cover was neither
dense nor succulent enough for their requirements. The great
bulk of this large catch of deer mice were immatures and young
adults.
In spite of my limited data, I believe the original prairie was
capable of supporting a fairly high small rodent population. This
belief is supported by the findings of Smith (1940) working in
Oklahoma. He says that : “Although somewhat less food is avail¬
able in climax prairie, excellent cover is present and a large
population of rodents is found.”
Table VI. Number of mammals caught, calculated density per acre, and
composition of population of a short-grass prairie relic,
October 17-20, 1941.
Hanson — Small Mammal Censuses
113
Sandy Field
Continuous farming of an inadequate topsoil had reduced
this field to shifting sands. It is now slowly returning to a modi¬
fied prairie. At the time of the census, scattered clumps of panic
grass ( Panicum Scribnerianum) were the dominant cover.
Prairie lespedeza ( Lespedeza capitata), a species of puccoon
(. Lithospermum croceum) , and spiderwort ( Tradescantia re-
flexa) also occurred. The field is planted to pines, but only ten
per cent of the quadrat supported trees over three years of age.
The eight- to ten-year-old trees have not yet modified the sur¬
rounding ground cover.
Though cover was at a minimum, prairie deer mice proved
to be surprisingly abundant (Table VII).
Table VII. Number of mammals caught, calculated density per acre, and
composition of population of a sandy field, October 7-10, 1941.
Juniper Bluff
Depressed juniper ( Juniperus communis depressa) , ar¬
ranged in a somewhat checker-board fashion, together with
prairie relics form one of the unique plant associations on the
Prairie du Sac area. This type is found on the extremely dry
and westerly-facing slopes overlooking the Wisconsin River.
Though cattle-grazing had caused the invasion of such weeds as
evening primrose, mullen, and hoary vervain, a number of prai¬
rie species still flourished. Among the latter were: little blue-
stem grass ( Andropogon scoparius) , St. John’s wort ( Hyperni -
cum) , prairie bluebell (Campanula) , and lead plant (Amorpha
canescens). This habitat was the only one censused in which
both species of Peromyscus were distributed rather evenly
throughout the quadrat (Table VIII). The author has not en¬
countered a reference in the literature to any other habitat free¬
ly populated by both species of deer mice.
114 Wisconsin Academy of Sciences , Arts and Letters
The census plot was only 240 by 240 feet due to the configura¬
tion of the available area.
Table VIII. Number of mammals caught, calculated density per acre, and
composition of population on a juniper bluff, October 15-18, 1941.
Red Cedar — Red Oak Pasture
This woodlot was composed of an open stand of red cedar and
red oak occurring in about equal numbers, with a few scattered
depressed junipers. The ground cover was sparse, made up
chiefly of an intermixture of bluegrass, a panic grass and an
occasional clump of little bluestem grass. A few small scattered
patches of prickly ash and black raspberry were all that re¬
mained of the shrubs. Among other herbs and weeds present
were wild bergamot, prairie clover (P etalo sternum) , prairie
lespedeza, St. John’s wort, hoary vervain and mullen.
The drastic effect of long continued grazing of woodlots on
small mammal populations is evident in Table IX below. The
only apparent reason for the woodmouse population holding up
was the excellent places of retreat afforded by the litter of
needles under the cedars and amongst the depressed junipers.
Table IX. Number of mammals caught, calculated density per acre, and
composition of population of red cedar — red oak pasture,
October 2-5, 1941.
Hanson — Small Mammal Censuses
115
White Birch-Prickly Ash
White birch and prickly ash were the two chief woody species
growing on a north-facing slope that was censused in late Oc¬
tober. At one time an even-aged stand of red oak timber had
occupied the site, but had been cut over some years previous to
the time of the census. After the cutting occurred the slope had
evidently been pastured by cattle. Under their selective brows¬
ing these two species, unpalatable to cattle, gradually assumed
dominance.
Since the leaves of neither the birch or ash tend to build up
a heavy layer of leaf mold, this cover type offered little attrac¬
tion to small mammals. Thus the small mammal population of
this woodland was unusually low (Table X). The three shrews
were taken near old rotten stumps of oak trees.
Table X. Number of mammals caught, calculated density per acre, and
composition of population of a white birch — prickly ash woodlot,
October 24-27, 1941.
Red and White Oak Woodlot
(severely grazed)
The low mammal density found in this woodlot (Table XI)
indicates that constant grazing by cattle may be disastrous to
small mammal populations. Cattle had eradicated almost every
shrub in this woods and the resultant packing of the topsoil had
probably excluded the locally rare pine mouse (Pity my s pinetor-
um). Even the woodland deer mouse population was markedly
low. Fox squirrels still remained abundant in this woods, and
probably benefited by the lack of cover.
i
116 Wisconsin Academy of Sciences , Arts and Letters
Table XI. Number of mammals caught,, calculated density per acre, and
composition of population of a red and white oak woodlot
(severely grazed), Oct. 24-27, 1941.
Red and White Oak Woodlot
(moderately grazed)
This woodlot differed from the one discussed above mainly
as to the degree of grazing to which it had been subjected.
Prickly ash and a species of Rubies were the only remaining
shrubs of any abundance. A thick layer of leaf mold was be¬
lieved to explain the survival of pine mice in this woodlot, since
this species in Wisconsin has been recorded only from woods in
which litter remained. The woodland deer mouse population
(Table XII) was similar in density to that which Burt found in
an oak-hickory woodlot (11 per acre in November) in Michigan.
Flying squirrel populations are not calculated on an acreage
basis, as little is known of their mobility, but the presence of a
greater number of den trees is thought to account for their
greater abundance in this woods.
Habitat Preferences
Pygmy Short-tailed Shrew — Cryptotis parva parva (Say)
The author is aware of only one previously published record
reporting this species from Wisconsin. This record consists of
the remains of an individual found in an owl pellet collected at
Prairie du Sac. (Errington, Hamerstrom, and Hamer strom,
1940). Intensive fieldwork may reveal that it is more widely
distributed and common in Wisconsin than the lack of records
would indicate.
The single specimen in the author's collection was found dead
on the Sauk Prairie on December 15, 1942, by Albert Gastrow of
Prairie du Sac. It had been killed by a red fox, as the trail sign
clearly indicated, and then had been tossed aside. The finding of
Hanson — Small Mammal Censuses
117
this specimen on prairie is in agreement with its preference for
dry habitats.
Table XII. Number of mammals caught, calculated density per acre, and
composition of population of a red and white oak woodlot
(moderately grazed), Oct. 25-28, 1941.
Short-tailed Shrew — Blarina brevicauda brevicauda (Say)
Short-tailed shrews on the Prairie du Sac area are apparent¬
ly chiefly limited in their distribution to areas of bluegrass and
woodlands having numerous fallen logs and a thick layer of leaf
mold (Table XIII). In these situations they inhabit the run¬
ways made by themselves and by the resident mouse population,
and in all likelihood are dependent on them for protection, as
well as for insect food or an occasional mouse. Hence, shrew
populations are probably relatively secure from horned owl pre¬
dation. (“Represented in 2.7% of the total pellets and
stomachs [examined] ” — Errington, Hamerstrom, and Hamer-
strom, 1940). Predation likely occurs when they make short
excursions away from these sheltered trails.
Table XIII. Populations and relative abundance of short -tailed shrews in
five cover types, October 2-28, 1941.
118 Wisconsin Academy of Sciences , Arts and Letters
Least Weasel — Mustela rixosa aUegheniensis (Rhoads)
Records of the least weasel in southern Wisconsin are too
few to enable one to deduce the pattern of its distribution in this
portion of the State. Swenk (1926), in the most recent review
of the species, lists the following Wisconsin records : Pierce Co.,
Prescot 1; Racine Co., Burlington 1; Sauk Co., Sumpter town¬
ship, 2 ; Merrimac 1. After his paper was published, remains of
another specimen was reported in an owl pellet from Stoughton,
Dane Co., by Errington, Hamerstrom and Hamerstrom (1940).
Phillip Wright of the University of Wisconsin is known to have
secured two in the University Arboretum. During the winter of
1943-44 a third specimen was taken in the arboretum by Robert
A. McCabe, biologist in charge. I am indebted to him for fur¬
nishing his data on this specimen.
The data on five more least weasels recently taken in Sauk
Co. are given in Table XIV. These specimens were obtained
from farmers by Mr. Ed Ochsner of Prairie du Sac, and at least
four of the five wTere killed by the farmers when removing corn
shocks from the fields.
Table XIV. Data on six additional least weasels taken in Wisconsin.
* These weights are low as the specimens were eviscerated when received.
Hanson — Small Mammal Censuses
119
Descriptions of the pelage of these six specimens are given
below:
Individual
(Collector’s
Number)
638 Entirely white except for brown hairs on the distal half of tail.
653 Entire back and sides brown; ventral portion of the body white, the
white extending slightly higher on the head and neck region and
present on the dorsol side of the toes of tide fore legs.
688 Pelage entirely white including the tip of the tail.
651 Pelage midway between the white of winter and the brown of sum¬
mer. The brown limited to the dorsal % of the body and extending
down the dorsal sides of the fore and hind legs and tad. A white
patch above the nose and extending around the eyes as a cireumor-
bital ring; a larger white patch in front of each ear. Ears brown,
slightly tipped with white. Sides of neck white and numerous white
hairs intermixed with the brown of the back where it joins the white
sides.
653 Similar to No. 652.
1 Similar to No. 652.
Harvest Mouse — Reithrodontomys megalotis pectoralis * Hanson
A local reconnaissance was made on the Sauk prairie, in addi¬
tion to the censuses in Columbia County, to gather further in¬
formation regarding the habitat preferences of the harvest
mouse. One of the cover types trapped in Sauk County was a
tall stand of ragweed in a sandy fallow field. On entering this
field two harvest mice were observed running about. One of
these mice was captured by hand, while subsequent trapping
yielded an additional three. As no other species of mice were
caught in that field, it would appear that the harvest mice like a
partial over-head canopy and a relatively herb-free, hard-packed
ground surface that permits freedom of movement. Their ap¬
parent preference for the cultivated counterpart of this eco¬
logical niche, alfalfa fields, is evident from Table XV. They were
also more abundant in this habitat relative to the total popula¬
tion than in any of the other cover types.
This mouse is fairly common about Prairie du Sac. Hence,
it is surprising that specimens had not been reported from Wis¬
consin prior to 1941. Errington (1932) and Errington, Hamer-
strom, and Hamerstrom (1940) did not report it in owl pellets
collected from the Prairie du Sac region. This species was, how¬
ever, frequently recorded in owl pellets that they studied from
* A paper by the author relating to the discovery of this species in Wisconsin and its dis¬
tribution and taxonomy has been published by the Chicago Museum of Natural History. See
Literature Cited.
120 Wisconsin Academy of Sciences , Arts and Letters
Des Moines and Ames, Iowa — localities that lie well within the
previously known range of the harvest mouse.
The author examined roughly 100 owl pellets collected on
April 1, 1942, from a Scotch pine plantation on the Sauk prairie,
Sauk County, in which five long-eared owls had wintered. In
these pellets were found skulls of 77 Microtus , 25 Peromyscust
and 17 Reithrodontomys , thus indicating that the harvest mouse
was freely taken by long-eared owls.
Table XV. Population and relative abundance of harvest mice in eight
cover types, September 21-October 20, 1941.
Prairie Deer Mouse — Peromyscus maniculatus bairdi
(Hoy and Kennicott)
The prairie deer mouse was probably the most abundant
native mouse on the Prairie du Sac area in the fall of 1941. Like
the harvest mouse, this species seemed to prefer situations where
the immediate ground cover varied from light to moderate den¬
sities. This is shown by the fact that they attained a fairly high
density in a sandy field having as its chief cover scattered plants
of panic grass. Other species of mice seem to be unable to popu¬
late, at least in any densities, such xeric and exposed habitats.
As pointed out by Johnson (1926), the prairie deer mouse has
probably increased in abundance and extended its range as a
result of cultivating the land; and investigations will probably
show that prairie deer mice are confined to early stages of the
prairie succession on uncultivated lands. The distribution of
this species on the Prairie du Sac area supports these conten¬
tions (See Table XVI).
Hanson — Small Mammal Censuses
121
Table XVI. Population and relative abundance of prairie deer mice m
eight cover types, September 21— October 20, 1941.
Woodland Deer Mouse — Peromyscus ieueopus
noveboracensis Fischer
Woodland deer mice were trapped in every census area that
supported a few trees or shrubs. One female had made her nest
for five new-born young in a paper wasp nest hanging in a clump
of hazel-bush. At least a portion of the habitat in cover of a
woody nature seemed requisite to satisfy some demand in this
mouse.
A female, which had her young in a nest of corn silk inside
of a corn-shock, was the only individual encountered a consider¬
able distance from timber or brush. Johnson (op. cit.) also re¬
ports capturing a wood mouse in a cornfield a quarter of a mile
from the nearest woodland. However, some individuals which
have home ranges along the borders of woods range out into
Table XVIL Population and relative abundance of the woodland deer
mouse in seven cover types, October 2-28, 1941.
122 Wisconsin Academy of Sciences , Arts and Letters
adjoining fields (Blair). While trapping the bluegrass-sweet
clover fields a number of wood mice were taken (Table XVII),
but these were generally caught in traps less than 35-40 feet
from the forest edge.
Field Vole — Microtus ochrogaster Wagner
The northern and western limits of the range of this species
in the midwest is still in need of careful exploration. Field in¬
vestigations by the author in central and western Wisconsin and
in southeastern Minnesota have suggested the possibility that
the range of Microtus ochrogaster is coincident with that of the
harvest mouse, Reithrodontomys megalotis pectoralisf in this
region.
It was observed that Microtus ochrogaster was the common
vole at the localities where harvest mice occurred, while locali¬
ties that did not yield harvest mice also failed to yield M . ochro¬
gaster; replacing this vole in the same ecological niche was the
meadow vole, Microtus pennsylvanicus.
Microtus ochrogaster may be the most abundant vole over
the uplands and sand prairies of the driftless region. It proved
to be the only vole common to the upland fields in Westpoint
Township, Columbia County, and on the Sauk prairie, Sauk
County, both on the eastern border of the driftless area. In
western Clark County, Schmidt (1931) found Microtus ochro¬
gaster only on sandy plains and slopes of sandstone mounds
where there was no heavy covering of grass ; Microtus pennsyl¬
vanicus was taken in hayfields, pastures, and other well-watered
habitats.
Records of the field vole from western Wisconsin are limited,
but they indicate that this species occurs there freely. Allen
(1936) mentions obtaining specimens of the field vole in Vernon
County. In the fall of 1942 the writer trapped a number of these
voles, as well as three harvest mice, from an upland alfalfa field
east of La Crosse in La Crosse County during one night of trap¬
ping.
According to Thwaites (unpublished map 1944) the western
limits of the driftless area are now recognized as extending not
beyond the tops of the Mississippi River bluffs on the Minnesota
side. Since data available suggests that the harvest mouse, R. m.
pectoralis, is found only in or on the periphery of the driftless
i
Hanson — Small Mammal Censuses
123
region (Hanson 1944), it was of especial interest to find a grain
stubble-field in a valley near Hokah, Houston County, Minne¬
sota, which was inhabited by both species of voles as well as
harvest mice. Allen (1936) also reports finding both species of
Microtus in a similar valley near Caledonia, Houston County.
However, at three localities a few miles west of Hokah and well
beyond the edge of the driftless area, the writer was unable to
trap either the harvest mouse or the field vole. At these locali¬
ties (two near Spring Grove, Minnesota, and one 14 miles south¬
west of Preston, Minnesota) Microtus pennsylvanicus and Per -
omyscus maniculatus were the only species of mice obtained.
The field vole and harvest mouse are apparently absent from
northeast Iowa (Allamakee and Winnesheik Counties) where
Microtus Pennsylvania cs is abundant as Dr. Sherman Hoslett
of Luther College, Decorah, Iowa, was unable to secure an
example of this species during an intensive five-year study of
the mammals of these two counties. Thus, judging from the evi¬
dence available, it seems that the ecological or geological factors
determining the distribution of the harvest mouse in the south¬
east Minnesota-northeast Iowa region may also be operative in
the case of Microtus ochrogaster .
Cory (1912) notes that prairie voles are commonly found in
clover and alfalfa fields, a preference the Prairie du Sac census
supports. Stubble-fields become increasingly inhabitable to this
species as quackgrass and other weeds gain a foothold, but maxi¬
mum densities are attained in bluegrass areas (Table XVIII).
Table XVIII. Population and relative abundance of the field vole in five cover
types, September 21-October 19, 1941.
Meadow vole — Microtus pennsylvanicus pennsylvanicus (Ord)
The only habitat to yield more than two stray meadow voles
was a Carex stricta bog. Several other specimens were obtained
124 Wisconsin Academy of Sciences, Arts and Letters
from a another bog a few miles east of the Prairie du Sac area.
Since this species was found commonly only in Carex stricta , it
seems possible that it could become locally extinct through drain¬
ing and the gradual drying up of these bogs.
Table XIX. Population and relative abundance of the meadow vole in
three cover types, October 2-19, 1941.
Pine Mouse — Pitymys pinetorum scalopsoides
(Audubon & Bachman)
Pine mice collected in northern Clark County, Wisconsin, by
Franklin Schmidt were recently recognized as a new subspecies
by Hartley H. T. Jackson (1941). Since the two individuals col¬
lected by the author are not in a pelage comparable with the
type series from Clark County, the Columbia County specimens
are assumed to belong to the race scalopsoides. Additional speci¬
mens of pine mice have been taken in western Dane County
(Blue Mounds) by Phillip Wright (University of Wisconsin col¬
lections). Excepting mention of a specimen from Lynxville,
Crawford County, (Jackson op. cit .) no other published records
are available to reveal the distribution of this species elsewhere
in the state.
The habitat requirements of the pine mouse in Wisconsin are
apparently very specific as all records of this species to date are
from oak forests having a heavy carpet of litter and leaf mold.
Elsewhere in its range, according to Hamilton (1938), it has
been found in such diverse situations as sphagnum bogs and
rocky hills about caves. Hamilton (op. cit.) quotes Poole as
having found pine mice in Pennsylvania on an area having “light
sandy alluvial soils supporting scattered trees and shrubs.”
One of the two specimens taken on the Prairie du Sac area
was trapped above ground at the base of an oak tree, while the
other was caught in a trap set in an opened runway in the leaf
mold.
Hanson — Small Mammal Censuses
125
Table XX. Population and relative abundance of the pine mouse in a red
and white oak woodlot, October 25-28, 1941
House Mouse — Mus mas cuius mus cuius Linnaeus
House mice attained their greatest densities in cultivated
fields where they often were the most abundant species. When
their numbers about farm buildings were taken into considera¬
tion, there can be little doubt that they were the most numerous
mammal on the Prairie du Sac area. Because of their general
abundance in fields far from any farm buildings, it is difficult
to understand their comparative absence in owl pellets. One
reason may be that owl pellet studies usually represent the late
winter and early spring months, a period when house mice par¬
ticularly seek buildings for refuge ; another may be that the first
spell of severe cold weather greatly reduces the field inhabiting
populations.
The high density of this species found in the prairie relic was
probably due to an influx of individuals from the nearby area of
smartweed and foxtail which had an extremely high house
mouse population (Table XXI). However, it should be noted
that they were relatively uncommon in this undisturbed area.
Table XXI. Population and relative abundance of the house mouse in nine
cover types, September 21-October 20, 1941.
(moderately grazed)
126 Wisconsin Academy of Sciences , Arts and Letters
Cottontail — Sylvilagus floridanus mearnsi (Allen)
Method and Materials . — The method used to census cotton¬
tail rabbits was first employed by Durward Allen (1938-1939)
in Michigan. It consists of trapping and banding the largest
number of rabbits possible and securing a shot sample of the
population on the census area. From the ratio of banded to
unbanded rabbits in the sample to the total number banded, the
actual population is determined. This technique has been used
by Lincoln as an adjunct to estimating continental waterfowl
populations.
Forty “Pennsylvania type” box traps, as described by Ger-
stell (1937), were used for the census. All rabbits caught were
banded with ear tags which proved to be very satisfactory. Car¬
rots were found to be the best bait as they did not spoil quickly
in mild weather and were not as attractive to mice as ear or
shell corn.
Census Area. — The census area consisted of approximately
65 acres of woods and brushy cover on the south slopes of Black-
hawk ridge, and an area of second growth timber and brush-
lands adjoining its western base. The observed tendency of win¬
tering cottontails in southern Wisconsin to avoid cold windy
slopes made it unnecessary to extend the trap lines on to the
north slopes of the ridge. This latter area was not considered
a part of the winter range when computing the population. A
brief description of the cover types on the census plot and their
acreages are summarized below :
Cover Types Acreage
Ungrazed woods with an abundant understory of shrubs 14
Grazed woods containing scattered thickets of prickly ash,
blackberry and red cedar 21
Second-growth oak woods with a poor understory of shrubs 13
Heavy bluegrass, with scattered shrubs, young oaks and
stump sprouts (5 small areas) 16
Short grass prairie relic 1.5
Total 65.5
Trapping Operations. — Due to the diversity of the cover
types, weather conditions, and the irregular distribution of the
rabbit populations in the various coverts, trap movement pro¬
ceeded in no orderly fashion; instead, the traps were shifted
from place to place whenever their efficiency in catching un-
Hanson — Small Mammal Censuses
127
banded rabbits suffered a marked drop. In addition to these
variables in the procedure, one sector of the census area was
trapped continuously during most of the census period. The
number of traps used varied, and their efficiency was never
100% as mice sometimes ate the bait or sprung the traps. A
summary of the trapping operations is given in the table below :
Trapping Periods
Nov. 23-Dec. 7
Dec. 7 -Dec. 22
Jan. 9- Jan. 13
Jan. 13-Feb. 13
Traps in Use
30
38
13
37 (av.)
Trap nights
420
532
52
1148
Total 2100
A total of 71 rabbits were caught and of these four died in
the traps. The number of repeats was small because of the fre¬
quency of trap movement. Of the 22 rabbits that repeated, a few
were caught as many as three times, making the total number of
repeats twenty-nine.
Sampling. — Shooting was believed to be the most efficient
means by which an adequate sample of the rabbit population
could be secured in the shortest period of time, thereby reducing
any error resulting from movements of rabbits into or out of the
census area during the sampling period. It was also thought that
shooting would obtain a more representative sample than live
trapping which might be more apt to take an undue number of
rabbits having the trap habit. The latter point, however, still
requires further testing. Other sources of error that are present
in this technique of censusing have already been discussed by
Allen (op. cit.) and Dice (1941).
During the first shoot on February 14, a crew of eight se¬
cured only three rabbits. The sampling was continued until
March 22, but it was with the greatest difficulty that a sample of
twenty-one was secured.
Populations. — Twelve of the twenty-one rabbits shot carried
bands. As the total number of rabbits banded was known (71,
minus three that died in traps), the solution of a simple ratio
gave the approximate total population on the census area.
(71-4) 12
_ • _ 12 x = 1407 x = 117
x 21
128 Wisconsin Academy of Sciences, Arts and Letters
In the course of the fieldwork, remains or indications of old
kills of 11 rabbits were found. This number added to the 117
implies a peak fall population of at least 128 rabbits on the 65
acres of brushlands and woods, or a density of 2 rabbits per
acre. However, the average density for the entire winter would
be somewhat less.
Acknowledgements
This study was begun under a fellowship from the Wisconsin
Alumni Research Foundation, and was completed under a grant
from the American Association for the Advancement of Science,
awarded through the Wisconsin Academy of Science. During
the fieldwork I had the able co-operation of Albert Gastrow of
Prairie du Sac, who was censusing other species for the Wis¬
consin Conservation Department. His keen observations and
skill at “reading sign” contributed much to this study.
Literature Cited
Allen, Durward
1938. Ecological studies of the vertebrate fauna of a 500 acre farm in
Kalamazoo County, Michigan. Ecol. Monog., 8: 348-436.
1939. Michigan cottontails in winter. Journ. Wildlife Mgmt., 3: 307-322.
Allen, Phillip F.
1936. Microtus ochrogaster in Minnesota. Joum. of Mamin., 17: 291.
Blair, W. Frank
1940. A study of prairie deer mouse populations in southern Michigan.
Amer. Mid. Nat., 24: 273-305. 6 tables, 4 figures.
1940. Notes on home ranges and populations of the short-tailed shrew.
Ecology, 21: 284-288.
1940. Home ranges of the meadow vole in southern Michigan. Journ.
Wildlife Mgmt., 4: 149-161. 1 figure.
Bole, B. P. Jr.
1939. The quadrat method of studying small mammal populations. Cleve¬
land Museum of Natural History, Scientific Publications 5 (4) Dec.,
15-77.
Burt, Wlliam Henry
1940. Territorial behavior and population of some small mammals in
southern Michigan. Misc. Pub. No. 45, Museum of Zoology, Univ.
of Mich. 1-58. 2 plates, 8 figures, 2 maps.
Cory, Charles B.
1912. The mammals of Illinois and Wisconsin. Field Museum of Natural
History, Pub. 153, Zool. Ser., XI, Chicago.
Dice, Lee R.
1941. Methods for estimating population of mammals. Journ. Wildlife
Mgmt., 5: 398-407.
Hanson — Small Mammal Censuses
129
Errington, Paul L.
1932. Food habits of southern Wisconsin rap tores. Condor, 34: 176-186.
Krrington, Paul L., Frances Hamerstrom and F. N. Hamerstrom, Jr.
1940. Great horned owl and its prey in north central United States. Agr.
Exp. Sta., Iowa State College of Agriculture and Mechanical Arts,
Research Bui. 277: 757-850. 12 tables, appendix.
Gerstell, Richard
1937. Management of the cottontail rabbit in Pennsylvania. Part II. Pa.
Game News, No. 2, 8: 8-10, 32. 1 figure.
Goodnight, Clarence J. and Koestner, E. J.
1942. Comparison of trapping methods on an Illinois prairie. Joum. of
Mamm, 23: 435-438.
Hamilton, W. J., Jr.
1938. Life history notes on the northern pine mouse. Joum. of Mamm.,
19: 163-170.
Hanson, Harold C.
1944. A new harvest mouse from Wisconsin. Field Museum Natural His¬
tory, Zool. Ser.
Hoslett, Sherman S.
1940. Unpublished doctorate thesis on the mammals of northeast Iowa.
Univ. of Mich., Ann Arbor.
Jackson, Hartley H. T.
1941. A new pine mouse, genus Pitymys, from Wisconsin. Proc. Biol. Soc|
Washington, 54: 201-202.
Johnson, M. S.
1926. Activity and distribution of certain wild mice in relation to biotic
communities. Journ. of Mamm., 7: 245-277.
Nicholson, Arnold J.
1941. The homes and special habits of the wood-mouse. ( Peromyscus
leucopus noveboraceTisis ) in southern Michigan. American Midland
Naturalist, 25: 196-223.
Schmidt, F. J. W.
1931. Mammals of western Clark County, Wisconsin. Journ. of Mamm.,
12: 99-117.
Smith, Charles Clinton
1940. Succession on abandoned eroded farmland. Ecol. Monog., 10.
Swenk, Myron H.
1926. Notes on Mustela campestris Jackson, and on the American forms
of the least weasel. Joum. of Mamm., 7: 313-330.
Thwaites, F. T.
1944. Unpublished map of the driftless area. Univ. of Wis.
Townsend, Myron T.
1935. Studies on some of the small mammals of central New York. Roose¬
velt Wildlife Annals, 4, No. 2: 1-120. 22 figures, 8 plates, 4 maps.
Williams, Arthur B.
1936. The composition and dynamics of a beech-maple climax community.
Ecol. Monog., 6: 318-408. 16 figures.
s . ' ■
.
THE LAKE STURGEON, ACIPENSER FULVESCENS
RAFINESQUE, IN LAKE WINNEBAGO, WISCONSIN
Edw. Schneberger and Lowell A. Woodbury
Wisconsin Conservation Department, Madison, Wisconsin
Fishing for lake sturgeon, Acipenser fulvescens Rafinesque,
has been permitted for many years in the waters of Lake Winne¬
bago, Wisconsin. For the past three years the open season has
been from February 1 to March 1 with spearing as the only
legal method of fishing. The legal minimum length is 30 inches
and a season's bag limit is five fish. The regulations provide
further, that each person spearing sturgeon must purchase a
special tag for each fish. In order to collect data on the annual
harvest, creel census blanks on addressed and stamped postal
cards were furnished each person purchasing these tags. The
blanks provided space for the fishermen to record the length,
weight, and sex of each fish caught.
Lake Winnebago, the largest inland lake within the borders
of the state of Wisconsin, is located in the east central part of
the state. It is elongate, with a major axis of about 28 miles
lying in a north-south direction and a minor axis of about 10
miles lying in an east-west direction. The lake has a maximum
depth of about 21 feet and an average depth of about 15 feet
(Juday 1914).
Most of the spearing for sturgeon is done in two areas along
the eastern shore, one near Calumet Harbor and the other near
Stockbridge Harbor. A limited amount of spearing is also done
along the western shore near Neenah-Menasha, Wisconsin.
Schlumpf (1941) described sturgeon spearing in some de¬
tail and it is from his article that the following summary of the
techniques was made.
Spearing is done from portable shanties placed on the ice
one-half to four miles from shore and over the large mudflats
which are the feeding grounds of the sturgeon. A rectangular
hole about three by five feet is cut in the ice and the shanty
moved over the hole. The spearing is done in 13 to 16 feet of
131
132 Wisconsin Academy of Sciences , Arts and Letters
water. Broken pieces of pottery or white plates are often
dropped in the water so that the bottom is more easily seen and
the distance can be more readily estimated when a fish swims
into the area. Usually decoys intended to attract the sturgeon
are suspended about the hole in about ten feet of water. A
variety of decoys, ranging from oranges, lemons and ears of
corn to skillfully carved wooden images of sturgeon, is used.
The spear is so constructed that the spear and handle are de¬
tachable, although used as one unit. Props are attached to both
the spear head and handle. When a “hit” is made the handle
becomes detached from the spear and the fisherman can then
“play” the fish on the rope.
Materials and Methods
The creel census data, as mentioned earlier, were obtained
by furnishing each person who purchased a sturgeon tag with a
blank to which to record his catch. These cards were distributed
for the 1941, 1942, and 1943 seasons.
An estimate of the total take was made on the basis of the
assumed proportionality, viz :
Number of persons purchasing tags Number of fish Total
Number of persons reporting catch reported caught catch
Further information, especially with reference to food hab¬
its, length, weight, and age, was desired. Accordingly, Mr.
Homer E. Keane, an employee of the Wisconsin Conservation
Department, was detailed to Lake Winnebago during the 1942
sturgeon season, to collect the heads, viscera, and accompanying
data of as many sturgeon as possible. The heads were collected
so that the otoliths could be obtained for age determinations.
For several reasons this assignment was not as simple as it
seems. Many of the fishermen were secretive about their success
fearing that the “news” might attract too many other fishermen
to the vicinity of their particular fishing spot. Other successful
fishermen did not wish to part with the head of the fish stating
that they used it in the preparation of a special soup. Neverthe¬
less a total of 49 sturgeon heads and 11 alimentary tracts was
collected.
A description of the otolith and the methods employed in the
preparation of the otolith for reading is given under the section
on Ages.
Schneberger and Woodbury-— The Lake Sturgeon 133
Results of Creel Census
A summary of the data on creel census work is found in
Table I. Scrutiny of the table will show that the computed total
take was 788 fish in 1941, 467 fish in 1942, and 238 fish in 1943,
or a fairly proportionate decline. The cause of this decline is not
clear but depletion cannot be cited as a definite cause since there
are many factors that govern the take of sturgeon. Unfortu¬
nately it was impossible to obtain the unit effort expended by
the fishermen. There were, however, 110 less fishermen in 1942
and 320 less in 1943 than in 1941, the year of the greatest catch.
It is conjectured that in 1943 less effort was expended than in
1941 because of the general labor shortage and fishermen had in
general less free time to spend fishing. In addition the winter
Table I. Summary of creel census reports on sturgeon spearing in Lake
Winnebago for the years 1941, 1942, and 1943.
was quite severe and travel on the ice was difficult because of the *
deep snow. The season of 1942 was generally considered as a
poor year because the ice did not form until late in the winter
and the water remained turbid during most of the season.
The sucessfulness of a season is likewise reflected to some
extent in the size of fish reported. In 1942, the largest fish was
134 Wisconsin Academy of Sciences , Arts and Letters
88 pounds while in 1941, five fish which weighed over 100 pounds
each were reported. Their weights were 104, 105, 105, 112, and
135 pounds. In 1943, the largest fish reported weighed 120
pounds and the next largest weighed 90 pounds.
Ages of Lake Winnebago Sturgeon
Harkness (1924) in his study of the sturgeon used the oto¬
liths or earstones in determining age. Scales usually employed
for this purpose in the teleost fish are not present on the stur¬
geon and according to Harkness the vertebrae could not be used
because they failed to show annular markings. The opercles and
pectoral fins were examined by us, but these structures likewise
showed no annular markings. Therefore, in view of these find¬
ings, the otoliths were employed in the determination of age in
the present study.
The otolith is a small, curved, roughly triangular piece of
calcareous matter. In the specimens examined the length varied
from 7.5 to 12.3 millimeters. The composition varies from solid
homogenous calcareous material to a conglomeration of small
conical particles. The annular markings appear as more or less
definite dark bands or lines continuous across the otolith and
separated by finer broken lines. Some otoliths could be read with
comparative ease, others could not be read at all, while still oth¬
ers could be read up to a certain age but not beyond. An attempt
was made to determine the number of annuli by examination
under a binocular microscope with the otolith immersed in the
glycerine. The attempt was unsuccessful as the annuli could be
distingished only with difficulty and could not be counted accu¬
rately. Several other immersion fluids of high refractive index
were tried but all proved unsatisfactory.
An attempt was made to reduce the thickness of the otolith
on a geologist's “thin section” wheel but due to the curvature of
the specimens this method could not be used. After much trial
and error a method of preparation was evolved that gave excel¬
lent results and resulted in a permanent mount that showed the
annuli present in a satisfactory manner. This method is de¬
scribed in the following paragraphs.
The otolith was removed from a glycerine solution, drained,
and then passed through 95 per cent alcohol, clove oil and xylene,
remaining about five minutes in each liquid. Following this de-
Schneberger and Woodbury — The Lake Sturgeon 135
Table II. Length, weight, sex, and age of sturgeon from Lake Winne¬
bago, Wisconsin, taken during February, 1942.
• Otolith unreadable with any certainty.
dt Age near this value but exact figure uncertain.
-b Age greater than this value by indeterminate amount.
186 Wisconsin Academy of Sciences , Arts and Letters
hydration and clearing the otolith was placed in melted xylene-
free balsam until all xylene carried in with the specimen had
boiled off. It was then mounted on a slide concave, face down¬
wards, in a drop of melted balsam and allowed to cool.
With a small file and a sharp knife the otolith was then
thinned down by filing and scraping on the convex side until
microscopic examination of the concave surface showed clearly
the annular markings.
The dry balsam was then dissolved off in xylene and the
otolith mounted in fresh balsam under a cover glass with the
concave side upwards.
The otoliths were read with a compound microscope at a
magnification of 50 diameters and checked on a binocular micro¬
scope at various magnifications. They could not be read on a
micro-projection machine of the type ordinarily used for scales.
Out of a total of 49 heads, 47 pairs of otoliths were obtained
of which the ages of 35 were determined. The remaining 12
possessed various degrees of readability. The ages ranged from
14 to 40 ± 3 years. Due to the scantiness of the data and the
small numbers of fish in each year-class the average rate of
growth of each year-class could not be computed. The smallest
fish, 42 inches in length, was a male, 16 years old. The youngest
fish was also a male, 47 inches long, and was 14 years old. The
data indicates that the females grow at a slightly higher rate
and to a larger size than the males. The youngest female was
21 years old and was 48 inches long. A 22 year old female was
54 inches long. Table II gives the available data on length,
weight, sex, and age of all specimens whose otoliths were exam¬
ined.
The available data do not show the age at which maturity is
reached. The fish collected, however, were well above the mini¬
mum legal length of 30 inches since the smallest specimen col¬
lected was 42.5 inches long. Harkness (1924) however, stated:
“In all fish which were less than 22 years of age it was
impossible to determine the sex by macroscopic examina¬
tion of the reproductive organs. In older fish the sex was
readily determined. It is interesting to note that between
the ages of 20 and 25 years great changes occur in the
outward appearance of the sturgeon. The snout becomes
shorter and blunter ; the sharp points of the shield disap¬
pear; the shields themselves become smoother, and some
apparently are entirely resorbed. Without doubt these
Schneberger and Woodbury — The Lake Sturgeon 137
changes are associated with the attainment of sexual ma¬
turity which is reached apparently at about 22 years of
age. Although a female may become sexually mature at
this age, it is not until after the age of about 30 years that
she begins to produce a large number of eggs. Therefore,
the taking of fish of 30 years or less diminished greatly
the production of fry and is likely to result ultimately in
the complete depletion of the sturgeon.”
Comparative Growth of Lake Winnebago and Lake
Nipigon Sturgeon
As the age-length data on the sturgeon of Lake Winnebago
from our data and from Lake Nipigon (Harkness’ data) were
somewhat scanty a direct comparison of length at the same age
was not practicable due to the small number of age groups rep¬
resented in both samples.
In our data the definite ages varied from a minimum of 14
to a maximum of 31 and the relationship of length to age over
this range approximated a straight line. The age-length data
for the Lake Nipigon sturgeon over this same range, and for a
distance on each side also approximated a straight line. A
138 Wisconsin Academy of Sciences, Arts and Letters
straight line was therefore computed by the method of least
squares for both our data and those of Harkness (Figure 1).
The equations were as follows :
L = 34.06 + 0.8902 A M (Lake Winnebago)
L = 16.49 + 0.9798 A N (Lake Nipigon)
Where L = length in inches and A = age in years.
The Lake Winnebago equation was computed for the age
range 14 to 31 years and the Lake Nipigon equation for the
length range 10 to 40 years. A total of 33 pairs were used in
computing the Lake Winnebago curve and 18 for Lake Nipigon.
Table IIL Comparison of computed values of length for sturgeon of the
same age from Lake Winnebago and from Lake Nipigon.
Length (inches)
Table III shows the computed age-length values at intervals
over the range 14 to 31 years. The comparison indicates that
the Lake Winnebago fish grow somewhat faster than the Lake
Nipigon group. If this is true, it might be expected that the age
of maturity for the Lake Winnebago population is less than that
of the Lake Nipigon fish. Considerable more data are needed on
this point.
Food Habits and Parasites
Analysis of the stomach contents indicated that during Feb¬
ruary the sturgeon were feeding almost entirely on chironomid
larvae. Only a small proportion of other organisms such as
leeches and small mollusks were found. Table IV gives the re¬
sults of the stomach examinations.
Dr. C. A. Herrick, University of Wisconsin parasitologist,
was invited to examine the heads and alimentary tracts for para¬
sites. With the exception of a few trematodes found in three of
the tracts, the fish were free of parasites.
Schneberger and Woodbury — The Lake Sturgeon 139
Table IV. Results of examination of sturgeon stomachs taken from Lake
Winnebago, Wisconsin, during February, 1942.
Acknowledgements
The authors take this opportunity of expressing their sin¬
cere thanks to the many fishermen who furnished specimens for
study and returned the census cards ; to Dr. C. A. Herrick, Pro¬
fessor of Zoology of the University of Wisconsin, who examined
the specimens for parasites; and various conservation depart¬
ment personnel who assisted in various phases of the project.
Summary
1. On the basis of the creel censuses conducted it is estimated
that 788, 467, and 238 sturgeon were removed from Lake Winne¬
bago during the 1941, 1942, and 1943 spearing seasons.
2. Otoliths were collected for age determinations and a meth¬
od of preparing them for study is given.
3. The ages ranged from 14 to 40 ± 3 years. The smallest
and youngest fish was 14 years old, 47 inches long and weighed
28 pounds. The largest fish was 62 inches long, weighed 81
140 Wisconsin Academy of Sciences , Arts and Letters
pounds and was 40 ± 3 years old ; the exact age could not be de¬
termined with certainty. The females were slightly larger than
the males.
4. Analysis of the food found in the alimentary tract indi¬
cates that the sturgeon feed mainly on chironomid larvae during
February.
5. The specimens collected were relatively free of parasites.
Literature Cited
Juday, Chancey
1914. The inland lakes of Wisconsin. The hydrography and morphometry
of the lakes. Bull. No. XVII, Sci. Ser. No. 9., Wis. Geol. and Nat.
Hist. Survey, Madison, Wisconsin
Harkness, W. J. K.
1924. The rate of growth and the food of the lake sturgeon ( Acipenser
rubicundus Le Sueur) . Univ. of Toronto Studies, Pub. Ontario Fish.
Res. Lab., 18: 15-42.
Schlumpf, Charles A.
1941. The spearing of sturgeon in Lake Winnebago. Wis. Cons. BulL, 6:
33-36.
I
THE BUR OAK OPENINGS IN SOUTHERN WISCONSIN
A. B. Stout
The Neiv York Botanical Garden
A Typical Oak Opening.— Bur oak openings were the princi¬
pal timbered lands over a considerable part of southern Wis¬
consin when this region was homesteaded about one hundred
years ago. Today only a few remnants of these once numerous
natural parks still survive. One of these, about 50 acres in ex¬
tent and still in good preservation, is situated a few miles to the
north of the village of Albion in Dane County. A similar grove
now of smaller area is located about a mile to the southwest.
The illustrations (Plates 1 and 2), from photographs taken in
this grove in 1941, show the stately grandeur and the rugged
beauty of natural stands of this type of tree growth.
In this particular oak opening the trees are, I believe, all bur
oaks ( Quercus macrocarpa Michaux) ; but in some of the other
oak openings of the area and especially on the belt of moraines
there were trees of the white oak ( Quercus alba L.). These oaks
are all broad-topped and so spaced that seldom are the branches
of two trees interlocked. Also they are rather uniform in size.
There are no young trees or shrub growth anywhere in this
grove nor has there been such growth here for at least one hun¬
dred years. Between the trees there is the firm turf of native
grasses that has never been disturbed by cultivation. The entire
area of this grove is almost level, as are the reaches of formerly
prairie land that lie adjacent to the grove and which continue
for some distance immediately to the east and the northeast. But
many of the openings of the region were on the more rolling
and undulating uplands. A small, shallow, and rather sluggish
stream (Saunders Creek) flow's close to the south of this oak
opening and along its banks, both above and below the grove,
there are flat marshy grasslands that are often of considerable
extent and occasionally there are areas of tamarack swamp.
These lowlands and their water-table are, as a rule, only slightly
below the general level of the uplands. Marshes are abundant
141
142 Wisconsin Academy of Sciences , Arts and Letters
throughout much of the prairie-oak opening area that was glaci¬
ated and on which the drainage is geologically still young.
It seems to the writer that the trees in this grove are scarcely
any larger today than they were fifty years ago. The present
owner, Mrs. D. L. Babcock, is the daughter of Jacob Langworthy
who in the year 1842" became the owner of the farm which in¬
cludes this grove. She has resided on this farm for 85 years and
her recollection is that the character of this oak opening has
remained unchanged during all this time. It is known that
“prairie fires,, burned over this area both before and for some
time after the arrival of the early settlers. Storms have broken
down or uprooted some of the trees ; but except for the removal
of such trees no wood has been cut in the grove. About 50 years
ago nearly 100 of the trees were blown down at one time and
during a storm in 1941 nearly 30 trees were uprooted. The
counts that have been made of the annual rings of growth of
these trees indicate that the present age of most of the trees is
at least 200 years. The owners have taken an unusual and com¬
mendable pride in this grove that has prompted them to keep it
intact. For about 90 years its area has been pastured by cattle
and horses and for some of this time by sheep but never by
swine.
Oak Openings in Wisconsin. — The Babcock Oak Opening as
it stands today is typical of the groves which once covered a con¬
siderable part of an extensive area in Wisconsin. This region
extended across the entire southern boundary of the state.
Northward its width from east to west decreased, with irregular
border limits, until it terminated near Rush Lake. Roughly the
entire area in Wisconsin comprised about 5,000 square miles and
it formed a broad-based wedge that projected northward into
and almost through a wide belt of more dense forest growth in
which oaks were, and still are, the dominant species.
Dane County, in the southeast corner of which is the town¬
ship of Albion, is situated near the center of the area of oak
openings. Rock County lies partly adjacent to Dane County and
south of it. These two counties were quite typical of the best
developments of the prairie-oak opening vegetation in Wiscon¬
sin.
* The first four white settlers in the town of Albion arrived during the summer and autumn
of 1841.
Plate 1. View near the border of the Babcock Bur Oak Opening, looking eastward across an area of for¬
mer prairie. In the distance a woodland of second growth is in sight. Photo in 1941 by the author.
Plate 2. View looking westward across a section of the Babcock Bur Oak Opening near Albion, Wiscon¬
sin. Photo in 1941 by the author.
Stout— Bur Oak Openings in Southern Wisconsin 143
Early Records for Dane County. — The notations with the
early land surveys of Dane County record that the areas of for¬
est growth were mostly scattering oak trees which were re¬
ferred to as oak openings. In describing “the face” of Dane
County, Lapham in 1846 states that “there are no considerable
portions that can be called timber land, it being almost entirely
oak openings or prairie.” A “History of Dane County” (5),
published in 1880, makes both general statements regarding the
entire county and rather definite statements for each township
in respect to the character of the native vegetation. Some of
these statements may be quoted here.
“The prevailing timber of Dane County is small oak, oc¬
curring in patches or groves, constituting what is known
as oak openings” (p. 309). — “Bur Oak. This is perhaps
the most ornamental of our oaks. Nothing can exceed the
graceful beauty of these trees, when not crowded or
cramped in their growth but left free to follow the laws
of their development. Who has not admired these trees
in our extensive bur oak openings” (p. 128).
The statements for several of the townships may be quot¬
ed. (For Albion (36 square miles) : “The northeast part
is mostly prairie ; the southeast, oak openings ; the north¬
west, openings and marsh; and the southwest are open¬
ings, except sections 19 and 30, which are marsh.” —
For Dunkirk Township adjacent at the west of Albion:
“The lands in this town are diversified by oak openings,
prairie and marsh.” — For the township of Rutland
next west of Dunkirk: “The larger part of the land is
openings, while little, if any, may be termed prairie. The
soil is rich and productive. There is a lake known as
Island Lake which in early times was considered a curi¬
osity. It has an island near the center of about three
acres. This was once thickly wooded with good rock
maple trees with no others within twenty miles.” — For
the township of Oregon, third to the west of Albion:
“The surface in most places is beautifully undulating,
while in other places it is called hilly. It is principally
covered with bur oak, among which stood large white and
red oaks, and occasionally a large shellbark hickory. The
entire town was covered with a sweet and nutritious
grass, called blue joint.* As this grass was burned every
fall, and there was no underbrush of timber, a two-horse
* Evidently the name “blue joint” here refers to Andropogon jurcatus Muhl. For this species
Shantz and Zon (IS) give the common name “bluestem” and later Shantz (20) gives the name
“big bluejoint.” The species Calamagrostis canadensis also known as “bluejoint” was abundant in
the marsh meadows of Dane County.
144 Wisconsin Academy of Sciences, Arts and Letters
wagon could be driven through these openings with ease.
As these annual fires prevented the roots of the timber
from growing near the surface, the land was broken for
the same price for breaking prairie, hence it was claimed
the oak openings combined all the advantages of prairie
and timberland.” — For Blue Mounds, second township
from the south in the western tier of five townships and
about 30 miles from Albion: “The timber supply of the
town of Blue Mounds is perhaps as varied as can be found
in any locality in the county, there is oak in variety, black
walnut, butternut, hickory (bitter and sweet), poplar and
other timbers.” — For the town of York in the extreme
northeastern corner of the county : “The land of this town
is oak openings, with occasionally marsh, there being no
prairie within its borders.” — For Black Earth in the
northwestern corner of the county and second township
north of Blue Mounds : “Section 24 is mostly marshy land,
the remainder of the town being oak openings, with little
if any prairie.” — For Berry Township which joins
Black Earth: “This country, in its native condition was
timbered principally with oak, there being heavy growths
of white oak in the high lands, and bur oaks in the bottom
lands.” — For the township of Madison near the center
of the county: “The land is undulating, generally covered
with oak openings.”
The native forest vegetation over the other 26 townships was
quite like that of the nine townships for which the reports are
quoted. The eastern and western boundaries of the county did
not extend into the region of denser oak forest, but within the
confines of the county there were somewhat isolated areas of
such timber at the time when the areas were first settled. For
several of the townships, however, there are statements in this
publication of 1880 which refer to the changes in the character
of the timber that had already occurred since the area was
settled, and these will be noted later in this article.
Early Records for Rock County. — Of the native vegetation
in Rock County, which lies to the south of Dane County, there
are rather adequate statements in an early publication (2) that
appeared in 1856. Some of the most pertinent of the statements
will be quoted.
“This county is about equally divided between prairie and
oak openings. The trees are so scattering that men fre¬
quently make farms without felling — only girdling them
— besides the openings are annually burnt over, like the
Stout — Bur Oak Openings in Southern Wisconsin 145
prairies. On Rock River is a belt of timber and openings.
Groves are interspersed through the prairies at intervals,
besides which, points of openings jut into the prairie at
different places, thus rendering the outlines of the prairie
unequal, and at the same time bringing wood and timber
within a short distance to all its settlers ; in fact few men
on the prairie live more than three miles from timber.”
The record for several of the townships may be given here.
Of the five northern townships of Rock County, the middle one,
Fulton, lies adjacent to and directly south of Albion. For this
township :
“It has several small and beautiful prairies. The timber is
of large growth, suitable for sawing and building pur-
poses.” There are records of sawmills at the villages of
Fulton, Newville and Edgerton in this township at this
early date (1856). — For the township of Rock, the
third directly below Albion : “That part upon the east
side of the river is nearly all prairie, but that upon the
west side is mostly timber, some of it being very good,
though the greater part being oak openings.”
Records similar to these noted above could be quoted for the
counties or portions of them which lie to the east and to the west
of Rock County and to the immediate north of Dane County.
The Oak Openings in Relation to the Native Vegetation of
Wisconsin. — A brief but very excellent description of the
“classes” or “groups” of the main natural associations of plant
life in Wisconsin together with a map of their extent and dis¬
tribution was presented by Chamberlin (4). In discussing the
“oak group” Chamberlin (pages 177-181) makes the following
statement :
“This is most nearly related and most closely associated
with the prairie group. The prairies are rarely contigious
to any other form of aboreous vegetation. — The group
as here constituted includes both the 'oak openings’ or
'oak orchards/ and the denser oak forests. There are
sufficient reasons, however, for separating them into two
classes, as they indicate different, though allied, agricul¬
tural capabilities. The oak openings are most nearly re¬
lated to the prairies, while the oak forests graduate to the
following classes.” The “classes” here referred to are
designated “The Oak and Maple Group,” “Maple Group,”
“Maple and Beech Group,” and “The Hardwood and Coni¬
fer Group,” which are, in part at least, included in the
northern arm of what is now termed the northeastern
hardwood forest.
146 Wisconsin Academy of Sciences , Arts and Letters
Thus the bur oak openings comprised almost pure stands of
the one species, Quercus macrocarpa (with a sprinkling of Q.
alba especially on the higher lands) and they constituted the
most characteristic arboreal association that was in direct con¬
tact with the prairie. The belt of oak openings extended between
the prairies and the denser deciduous forests, in which there
was, and still is, a mixture of various species of trees, especially
red oak ( Quercus rubra), shellbark hickory {Cary a glabra),
large-toothed aspen ( Populus grandidentata) and such shrubby
underbrush as hazel nut {Corylus americana) and panicled cor¬
nel {Cornus paniculata) . The transition from oak openings to
the denser oak forest involved interpolations, intergradations,
and some intermingling of the two types of timber.
It may be noted that both the oak openings and the denser
oak forest of the oak group as described by Chamberlin combine
to form in Wisconsin and Minnesota the northern element of
what has more recently been termed the “oak-hickory associa¬
tion” and that this constitutes the western margin or zone of the
still more extensive “oak or southern hardwood forest.” It has
been stated that this entire oak forest “is probably the largest
hardwood forest in the Temperate Zones of the World” (15).
Of the character, location, migration and extent of this forest
there are numerous publications, especially those by Shantz and
Zon (15) and Shantz (20).
The Vanishing of the Prairies and the Oak Openings in Wis¬
consin. — The fertile prairie lands were ready for the plow of
the settlers. But on many of the homesteads in Dane County
and in neighboring counties the acreage was mostly oak open¬
ings and many of the trees were removed or at first merely
killed by girdling to provide land for cultivation. For a time
some of the oak openings were utilized as pasture lands for
cattle, horses, and sheep, especially if there were no lowland
meadows in a farm. Between the scattered trees of the oak
openings the native grasses flourished and provided excellent
grazing land.
Previous to 1900 many public gatherings, on such holidays as
Decoration Day and Fourth of July, and community picnics were
held in an oak opening where the checkered shade of the trees
contributed much to the comfort of all. But the extension of
cultivated farmland steadily reduced the area of the oak open-
Stout — Bur Oak Openings in Southern Wisconsin 147
ings. To some extent the needs for timber for building homes,
for the construction of rail fences, and for firewood contributed
to the removal of the grand old trees of bur oak and white oak.
Natural Reforestation by Second Growth. — While the bur
oaks were rapidly being decimated and the areas of oak open¬
ings were disappearing in the region about Albion, as elsewhere
in southern Wisconsin, there was a most remarkable spread and
increase of new or “second growth” stands of “black oaks.”
This noteworthy and conspicuous natural reforestation entirely
changed the character of the arboreal population in this par¬
ticular area during the years between 1850 and 1890. Here this
second growth was almost entirely composed of Quercus rubra
L. and Q. coccinea Muench. Thus a survey of the flora of Madi¬
son and vicinity (7) published in 1892 at a time when the second
growth forests were well advanced contains the following state¬
ments :
“Quercus rubra L. forms a considerable element in the
older forests of the region” and “Q. coccinea Wang, forms
the chief element in the oak forests of the region.” Quer¬
cus alba was reported to be present in “all woodlands of
the county” and to be next to Q. coccinea in abundance.
Quercus macro carp a was reported to be “represented in
all parts of the region by small clumps or single individu¬
als of medium sized trees.” These authors mention the
presence of only one other species of oak (Q. bicolor ,
Willd.) in Dane County and they make no mention of the
oak openings which had formerly been abundant about
Madison.
This second growth of timber appeared as seedlings which
were often in such numbers that they formed thickets over many
upland areas that were not cultivated or heavily pastured. Often
the second growth invaded oak openings and filled in about the
old trees of bur oak and white oak. As a result, in a span of
some 40 years, nearly every large farm in the area about Albion
possessed at least one “woodlot” of close-standing “black oaks”
of which many were no more than 12 inches in diameter at the
level of the ground. Some of these woods covered an acreage in
which there had previously been no, or at least few, black oaks
to serve as parent seed trees. But scattering trees of these oaks
and areas of rather dense woods which contained black oaks
were interpolated within the area dominated by oak openings,
especially near certain streams and lakes.
148 Wisconsin Academy of Sciences, Arts and Letters
Thus the second-growth oak forest composed of the so-called
black oaks became the principal natural association of tree
growth about Albion where the oak openings had formerly been
abundant. Perhaps the largest acreage of this second growth
was in existence here about 1880-1890. It was the rule that the
trees stood close together with no growth of grass between them.
Especially after 1890 many of these woodlands were cut over for
firewood or were entirely cleared. But fine stands of this timber
still exist. One such woodlot is shown against the horizon in the
middle of the view of Plate 1.
Scattered through many of the second-growth woods there
were, and still are, towering monarchs of white oak and some¬
what lower trees of the bur oak whose knarled trunks were
usually from three to four feet in diameter. These had existed
here when the site was an oak opening. In these trees the red¬
tailed hawks build their nests. The larger branches and trunks
are often hollow and in such cavities the screech owls nest, and
the abundant fox squirrels and the less frequent and more se¬
cretive flying squirrels make their homes.
The writer can attest that in these woods near the village
of Albion, as well as in the oak openings, he has rarely observed,
about one of the bur oak trees, any younger trees that could
have grown from its acorns. However when second-growth
woods were cut over and not severely pastured a “third-growth”
reproduction often contained some seedling reproduction of both
white oak and bur oak.
There has been some seed reproduction of both bur oak and
wdiite oak during the period of second growth in localities where
conditions favored such reproduction. One such area recently
studied by Chavannes (21) is located in the northwestern corner
of Dane County a few miles distant from the townships of Black
Earth and Barry in an area of the early oak openings. This par¬
ticular woodland covers sixty acres. The timber surrounds sev¬
eral small areas of hillside prairie the largest of which (Beech's
prairie) covers only one half of the area. Bur oak trees sur¬
round this island of relic prairie, and next to them is a stand of
white oak in a part of which there is a recent growth of linden.
Of both the bur oak and the white oak there are old wide-spread¬
ing trees as much as 250 years old which once formed an oak
opening. Now younger trees of the bur oak stand in a concentric
Stout — Bur Oak Openings in Southern Wisconsin 149
distribution about the plot of prairie and there are also younger
trees of the white oak. The study reveals that the growth of the
other arboreous species, such as linden, aspen and sumac, is an
invasion during the past one hundred years. No doubt there are
now many areas of second growth in the region of the oak open¬
ings in which there have been recent reproductions from the
seed of Quercus macrocarpa and Q. alba. But it is certain that
such reproduction has been relatively much less over the entire
area than the reproduction of other woody species, especially of
the so-called black oaks now found in the area.
Records of the Second Growth. — Mention of this develop¬
ment of second growth was made in some of the publications
already quoted. In the History of Dane County (5) in the report
of the township of Blooming Grove (second in the diagnonal
northwest from Albion) there are the following statements:
“In an early day there was but little timber in this town
in common with localities adjacent and what there was
was used with the utmost prudence. Some of the farmers
sowed locust seed to raise timber, but nature soon sup¬
plied the want and now there is enough and to spare of
white, black, and red oak and other kinds.”
Another record for the town of Perry in the southwest corner
of Dane County and the sixth township directly to the west of
Albion is of special interest:
“Largely rolling prairie, northeast part is principally roll¬
ing prairie. The southern part on the other hand, being
made up more of bluffs and low-lying bottoms. The town
in its native state was covered with brush and grubs,
there being scarcely enough timber to supply the wants of
the farmers, but now there is an abundance of young tim¬
ber, the growth of the last thirty-five years. It consists of
white, black, and red oak, including other kinds indige¬
nous to this part of the country.”
The development of second growth in the prairie-oak open¬
ing area in Wisconsin has been noted in numerous technical
publications of which one by Sargent (6) will here be quoted:
“The forest area has somewhat increased in the prairie
regions of the state since its first settlement and the con¬
sequent decrease of destructive prairie fires. The growth
of trees has gradually spread from the bottom lands of
the streams to the hills, and the oak forests on the up¬
lands have gradually encroached upon the prairie, losing
150 Wisconsin Academy of Sciences, Arts and Letters
their open, park-like character by the appearance of a
young growth which has sprung up among the old trees.”
That this increase of forest involved the spread and to some
extent the introduction of black oaks rather than the reproduc¬
tion of the original species of bur oak and white oak was later
recognized by Sargent (9) in the following statements which
refer to a wide area of the Mississippi basin as well as of Wis¬
consin :
“Forests of oaks, too, have spread over regions in the
basin of the Mississippi where prairies existed before the
white man checked the Indian fires which year after year
had swept them bare of trees. The oak forests of the
middle and southern states, although increasing in area,
are deteriorating, however, in composition, the white
oaks being gradually overpowered by the less valuable
black oaks, whose bitter acorns are left to germinate by
hogs which pasture in the forest and devour the sweet
acorns of the white oaks.”
This statement of the fact that there was a rapid and selec¬
tive reproduction of the black oaks applies to the developments
in Dane County noted above, but here the selective feeding on
acorns by hogs was never more than a most rare and incidental
occurrence.
Considerable attention has been given to the factors involved
in the reproduction and migration of species of Quercus. Gleason
(13, p. 120) discusses these matters but decides that the deter¬
mination of these factors is not sufficient to explain the distribu¬
tion and migration of the oaks in Illinois. More recently Kor-
stian (17) has determined many of the factors which affect the
production and the germination of the acorns and the survival
of the seedlings of several important species of oak, and he has
made application of this data to silvicultural methods. But it is
not fully evident how such factors operate in natural selective
and adaptive reproduction in which the inherent characters of
various species of oaks are involved.
It may be stated (a) that this extension of the forest was
the latest period in the general western advance of the oak for¬
est which had long been in progress in the Mississippi Valley;
(b) that this was at first favored by the cessation of prairie
fires; and (c) that the natural advance of the forest was then
checked and the area of the natural oak-hickory belt of timber
Stout — Bur Oak Openings in Southern Wisconsin 151
much reduced by the extension of agriculture. An excellent dis¬
cussion of “The Vegetational History of the Middle West” to¬
gether with a bibliography has been presented by Gleason (14).
The Natural Range and Variations of the Bur Oak . — The
species Quercus macrocarpa is distributed over a wide area of
the United States and Canada and in its population there are
noteworthy diversities in botanical characters, in habits of
growth that exhibit adaptations to habitats, and in associations
with other species of plants.
Trees of the bur oak are found over the entire range of the
southern hardwood forest and also over a considerable part of
the northeastern hardwood forest as these are mapped in the
Atlas of American Agriculture (15). The climax in the stature
of trees of this species is reached in the rich bottomlands of
southern Indiana and Illinois in the southern hardwood forest
where individual trees reach a height of 170 feet and a trunk
diameter of 6-7 feet (9).
Throughout most of their range the trees of the bur oak are
scattered among trees of other species and the associations in¬
volve a considerable number of species. So general is this habit
that one writer (22) makes the following statements:
“Bur oak never grows in dense stands, but as individuals
or in groups associated with other bottomland trees such
as pin oak, white oak, basswood, willow, cottonwood,
black walnut, the hickories, elms and soft maples. It
grows well on rich, moist bottomlands and on lower
slopes, preferring areas where water is available but not
excessive. Of relatively slow growth, it reaches great
ages and is not considered mature before 200 to 300
years.”
In its mid-western range the bur oak reaches the western
limits of the tall grass prairies in western Nebraska — about 600
miles directly to the west of the bur oak openings of Dane
County, Wisconsin. Pound and Clements (10, p. 148) report on
the bur oak in this region as follows :
“Quercus macrocarpa is the sole species of oak which
grows over the entire state. It extends from the bluffs of
the Missouri to the canyon sides of the foothills. The indi¬
viduals exhibit the greatest variation in different habi¬
tats. In the deep forests of I and II* ' Quercus macro -
Refers to the “Wooded Bluff” and the “Prairie” regions in Nebraska.
152 Wisconsin Academy of Sciences , Arts and Letters
carpa’ is a tall commanding tree, which is usually the
principal element in the formation. Northward along the
Missouri the bur oak steadily decreases in size in forest
formation and becomes a conspicuous object along the
tops of the high dry bluffs. The front of the bluffs of both
the Niobrara and the Republican is covered almost ex¬
clusively with individuals of this species. At the base of
the bluffs they are usually small trees, 3-5 meters high.
But toward the top they decrease regularly in size, and
become diffusely branched, so that the tops of the bluffs
are covered with a dense thicket of low straggling bushes,
5-10 decimeters high.”
It is evident from these statements that in 1898 the stands
of bur oaks in Nebraska were quite different from those of the
oak openings in Wisconsin. They were much more diverse in
habits of growth and there was much greater natural reproduc¬
tion. Weaver and Kramer (19) report in 1932 that in Ne¬
braska “in many places the bur oak is invading the grassland”
and that “most of this migration and invasion has occurred in
the 70 years since the early settlement of eastern Nebraska and
the cessation of prairie fires.” They describe and illustrate (see
their Figure 2) as typical of the “forest margin in eastern Ne¬
braska” a “pure open stand” of bur oaks mostly 50 to 65 years
old that were rather widely spaced (10 to 40 feet) but yet stand¬
ing somewhat closer together than are the trees of the Babcock
grove at Albion, Wisconsin. These authors report for the root
system characteristic of the bur oaks in Nebraska that (a) there
is a rapid growth and deep penetration (as much as 3-5 feet the
first summer) of the roots of seedlings; (b) that as trees mature
the skeleton of larger roots is wide spreading, and much
branched, and hence occupies a very large volume of soil; and
(c) that fine much-branched rootlets clothe this framework. It
is noted that this widely spreading, well-branched root system
compensates for the low water content of the soil, provides a
means of successful competition against grasses and shrubs, and
contributes to a competition between trees of the bur oak that
results in the somewhat wide spacing noted even in pure stands.
Further to the north of Nebraska the bur oak extends into
the area of the short grass prairie and here in the cold dry areas
of Dakota and eastern Montana plants that are classed as Quer-
cns macrocarpa become merely low shrubs, and in the most
Stout — Bur Oak Openings in Southern Wisconsin 153
northern range of this species at Berens River in Canada the
members are described as bushes.
Oak Barrens . — Trees of the bur oak occasionally form the
chief arboreous vegetation on sandy areas where the soil is much
less fertile than the soils of the bur oak openings of Dane Coun¬
ty. In the volume of Minnesota Plant Life, MacMillan (11)
makes the following statement:
“The bur oaks in Minnesota, together with the black
oaks, form oak barrens. These wastes, covered with gro¬
tesquely branching trunks, form picturesque forests in
the central part of the state.”
But MacMillan (8, 11) makes no mention of any remnants of
the oak openings in Minnesota in the zone of the hardwood belt
that was in contact with the prairies.
In his “Notes on the Big Woods” of Minnesota, published in
1875, Winchell (3) states that the western boundary of this
forest
“is not well marked, the trees gradually becoming thinner
and smaller, and more and more restricted to the valleys
of the streams, till the country is changed to a treeless
prairie. Around the outskirts of the woods small oaks and
aspens constitute almost the only arboreal vegetation.”
His only mention of oak openings is in the statement that
“There is a species of oak that appears like red oak ( Quer -
cus rubra L.) that frequents the outskirts of the Big
Woods. It is sometimes associated with the bur oak in the
openings.”
In his studies of the vegetation of the inland sand deposits
of Illinois, Gleason (13) also describes a bur oak association
which occupied the depressions between sand ridges. The bur
oak was the principal tree, but trees of white oak and shellbark
hickory were also present. The stand of trees was somewhat
close and the trees were rather young (see his Figure 1, Plate
XVI). In this sand area Gleason found in 1910 that the trees
which were invading the prairies were black oaks, chiefly of the
species Quercus velutina. There were in this area no oak open¬
ings of the type of the Babcock grove in Wisconsin. In the dis¬
cussion of the Barrens of Illinois, Indiana and Iowa, Gleason
(13) notes that these areas are characterized by a sparse low
growth of scrub oak ( Quercus velutina ), hazel and wild plums.
It should be noted here that the “oak openings” near Toledo,
154 Wisconsin Academy of Sciences , Arts and Letters
Ohio, which were described by Moseley (18) also occupy a sandy
sirea partly covered with low sand dunes, that although several
species of Quercus were found on the area the bur oak was not
present, and that this particular association is more like the oak
barrens than the bur oak openings in Wisconsin.
The Ecological Status of the Bur Oak Openings. — Several
features of the oak openings in Wisconsin are characteristic and
conspicuous: (a) the trees are of nearly the same age and of
good tree-like stature; (b) the trees were scattered or separated
in a park or orchard-like disposition with dense sod of grasses
between them; and (c) there had been for many years no repro¬
duction from seed of the trees and no invasion by other woody
species.
The trees in these bur oak openings, judging from those now
in the Babcock grove, date back to about 200-250 years ago, a
rather short and recent period of time when the entire interval
of the post-glacial history of the area is considered.
Various writers have supported the view frequently ex¬
pressed from an early date and already referred to in this arti¬
cle, that the prairie fires of the Indians were an important fac¬
tor in destroying tree growth in the belt adjacent to the prairies
and that one result of this was the development of the oak open¬
ings. Gleason (14) has supported this view and described the
probable process as follows :
“The fires destroyed seedling trees at the west margin of
the forest, preventing further advance in that direction.
It is doubtful if they penetrated far into the forest, but
by destroying the undergrowth and killing the more sus¬
ceptible species, they gradually reduced the forest to the
park like condition known as oak openings'" (14, pp. 80-
81).
According to this view the oak openings in Wisconsin and in
neighboring states were remnants of an earlier and more dense
marginal forest of which the older of the bur oaks and white
oaks withstood destruction by fires.
But in the Babcock grove the character of the grove has re¬
mained quite unchanged since the last prairie fires swept the
area. During this time in the area of this grove there continued
to be no seed reproduction of the bur oaks already there; but
there was also relatively little reproduction of bur oaks and
white oaks over the entire area.
Stout — Bur Oak Openings in Southern Wisconsin 155
What became of all the acorns produced in this Babcock
grove during the past one hundred years? From the general
evidence at hand, especially summarized and presented by Kor-
stian (17), large numbers were eaten by rodents and weevils;
perhaps few germinated and had even a chance to live in com¬
petition with the sod ; and finally it may be that seedlings of the
bur oaks and of any invading woody species were destroyed in
the browsings of cattle, horses and sheep. It would seem that
the facts in this situation, as well as those for the decided se¬
lective reproduction of black oaks over white oaks, could yet be
determined by direct observation and experimentation, and also
that the matters of reforestation warrant such study.
It may be noted that the association of a dense sod of grasses
with a scattering distribution of trees is a somewhat unstable
and obligate relationship. An increase in the stand of the trees
will eliminate the grass beneath the canopy of the branches. But
the dense sod of grass roots and rhizomes make it difficult for
seedlings of hardwoods to become established.
The rather robust growth of the bur oaks in the oak open¬
ings of Wisconsin is no doubt due to the fact that the trees have
developed on rich fertile land that has received adequate rain¬
fall for tree growth. The area of the tall grass prairies bulges
eastward into southern Wisconsin and over most of Illinois.
Over a considerable part of this area the amount of rainfall has
in recent time become favorable to forest growth and the oak
forests which were advancing to the west had in 1850 already
become a belt of considerable width. The oak-hickory portion of
the oak forest belt covered (a) much of the fine farm land of
Ohio and Indiana, (b) portions of southern Michigan and south¬
ern Wisconsin, (c) parts of Minnesota, Iowa and Illinois, and
(d) portions of other states to the southwest.
Northward in Minnesota the entire oak belt became a narrow
strip along the western edge of the Big Woods and in its margi¬
nal contacts with the prairie there was rapid decrease in the
size of the trees (3). This decrease in the stature of the tree
growth was quite general and continuous along the entire west¬
ern fringes of forest in the Mississippi Valley and northward in
Canada. Here several hundred miles to the west of the Wiscon¬
sin oak openings there was not only sparse and scattered dis¬
tribution of woody species but also much reduction in stature.
156 Wisconsin Academy of Sciences , Arts and Letters
That other species besides bur oak and white oak may domi¬
nate “openings” is to be recognized. Sargent writing in 1882
and 1883 (6), states that the original forests of the oak belt in
Ohio and Indiana had already been “largely removed in the de¬
velopments of agriculture.” For Illinois he reported that the
forest growth of the prairie region “was confined to the narrow
river bottoms and occasional open park-like groves of bur, scar¬
let, red, black jack or post oaks, known as ‘oak openings\”
While many areas of this timber in Illinois have now disap¬
peared, as elsewhere in the Mississippi Valley, some areas of
them still exist. In his report on the flora of the Chicago area
published in 1927, Pepoon (16, p. 47) shows a photograph of a
typical bur oak opening and states that this type of association
was at that date characteristic of the bur oaks on the ancient
lake benches of the area.
Although trees of the bur oak are found as far south as cen¬
tral Texas, it seems that in that region other species of oak are
most frequent in the “open forests” and “cross-timbers” which
are adjacent to the dry prairies [Sargent (6), p. 540]. Also in
Indiana territory the timberlands that are interspersed with the
prairies are mostly post oak ( Quercus stellata Wang.: Quercus
obtusifolia Michaux.) and black jack oak ( Quercus marylandica
Muench.) and in their most western range there is the stunted
growth of these species which is characteristic of the “cross¬
timbers.” But these species disappear to the north near the
Cimarron River [Sargent (6), p. 543] and in Kansas and Ne¬
braska the bur oak becomes the most abundant species of tree.
Several hundred miles to the eastward the black jack oak ( Quer¬
cus marylandica) reaches its northern limit on the sand prairies
of central Illinois on areas where the bur oak is not present
(12).
The Matter of Terminology. — Under the term “opening”
Webster’s New International Dictionary, Second Edition, 1842,
gives the following definition : “A thinly wooded space, without
underbrush, in the midst of a forest, or grove ; as oak-openings.”
But the bur oak openings in Wisconsin were not in the midst of
a forest; they were most often surrounded by or bordering on
prairie grassland.
In the Century Dictionary and Cyclopedia (1900) there is
the following definition :
Stout — Bur Oak Openings in Southern Wisconsin 157
“Opening. 5. A clear, unobstructed or unoccupied space
or place; specifically, in the United States, a tract over
which there is a deficiency of forest, trees being not en¬
tirely wanting, but thinly scattered over the surface, as
compared with their abundance in an adjacent region.
The word is most frequently used with this meaning in
Wisconsin and neighboring states on the west and as the
scattered trees are frequently oaks ( Quercus nigra*
jack-oak, and Q. obtusifolia ,** post oak, are the most com¬
mon species) such openings are often designated as oak
openings. Similar tracts in the more southern states, es-
specially in Kentucky, are called barrens and oak bar¬
rens
There follows a quotation from Cooper's novel, The Oak Open-
ingsy in which there is mention of the bur oak. The two species
of Quercus mentioned in the quotation above are the principal
oaks of the Cross-Timbers area in Texas and Oklahoma, but
neither was present in the extensive oak openings in Wisconsin
nor is now found in the state.
It appears that the term “oak orchard" employed by Cham¬
berlin (4) has had rather limited use in the literature of oak
openings, and that the terms “park" and “grove" have rather
wide applications which include other types of tree growth. The
term, chaparral (15, especially Figures 6 and 7), is especially
applied to broad-leaved woodlands of the southwest which range
from “an impenetrable thicket of low shrubs to open oak stands"
some of which may somewhat resemble the oak openings of Wis¬
consin but are entirely composed of different species.
Since the oak openings of Wisconsin constituted a somewhat
definite type of prairie grassland and oak forest association in
which the bur oak was more abundant than the white oak it
seems suitable to apply the term “bur oak openings."
A Commemoration of the Oak Opening in Literature. — The
bur oak openings received special mention and distinction in the
historical novel The Oak Openings which was written by James
Fenimore Cooper in 1848. The scene of the beginning of the
story in the year 1812 was in a bur oak opening on the banks
of the Kalamazoo River in Michigan. The description is as fol¬
lows :
“The country was what is termed ‘rolling/ from some
fancied resemblance to the surface of the ocean, when it
= Quercus marylandica Muench.
= Quercus stellata Wang.
158 Wisconsin Academy of Sciences , Arts and Letters
is just undulating with a long ‘ground-swell/ Although
wooded, it was not, as the American forest is wont to
grow, with tall straight trees towering toward the light,
but with intervals between the low oaks that were scat¬
tered profusely over the view, and with much of that air
of negligence that one is apt to see in grounds, where art
is made to assume the character of nature. The trees,
with very few exceptions, were what is called the ‘burr-
oak/ a small variety of a very extensive genus ; and the
spaces between them, always irregular, and often of sin¬
gular beauty, have obtained the name of 'openings/ the
two terms combined giving their appellation to this par¬
ticular species of native forest, under the name of ‘Oak
Openings/
“These woods, so peculiar to certain districts of coun¬
try, are not altogether without some variety, though pos¬
sessing a general character of sameness. The trees were
of very uniform size, being little taller than pear-trees,
which they resemble a good deal in form; and having
trunks that rarely attain two feet in diameter. The vari¬
ety is produced by their distribution. In places they stand
with a regularity resembling that of an orchard; then,
again, they are more scattered and less formal, while
wide breadths of the land are occasionally seen in which
they stand in copses, with vacant spaces, that bear no
small affinity to artificial lawns, being covered with ver¬
dure. The grasses are supposed to be owing to the fires
lighted periodically by the Indians in order to clear their
hunting-grounds/’
This excellent description of an oak opening was based en¬
tirely “on the evidence of documents” furnished to Cooper by
the “bee hunter” who was an important character of the novel,
and later a well-known citizen of Michigan, General Benjamin
Boden.
In the concluding chapter of the novel The Oak Openings ,
Cooper tells of his journey during the summer of 1848 from his
home pear Cooperstown, N. Y., to Kalamazoo. This, he states,
was “an occasion which offered to verify the truth of some of
our pictures, at least by personal observation.” The portion of
this journey from Detroit to Kalamazoo was by railroad and of
the natural scenery Cooper makes comment as follows :
“The whole country was a wheat-field, and we now began
to understand how America could feed the world. Our
road lay among the ‘Openings’ much of the way, and we
found them undergoing the changes which are incident to
Stout — Bur Oak Openings in Southern Wisconsin 159
the passage of civilised men. As the periodical fires had
now ceased for many years, underbrush was growing in
lieu of the natural grass, and in so much those groves are
less attractive than formerly ; but one easily comprehends
the reason, and can picture to himself the aspect that
these pleasant woods must have worn in times of old.”
At Kalamazoo, Cooper found that “Those who had laid out
this village, some fifteen years since, had the taste to preserve
most of the trees” and that the houses and grounds were “pleas¬
ant to the eye, on account of the shade, and the rural features
they present.” But in this year of 1848 Cooper evidently saw
few surviving trees of the bur oak openings that existed in the
area about the Chateau au Miel 36 years earlier and evidently
he did not find any sizable area of the oak openings still in a
natural condition. But at this time there were thousands of acres
of such oak openings in Wisconsin.
In regard to the present status of bur oak trees in the area
about Kalamazoo the writer has received the following state¬
ment from the Forestry Department of the City of Kalamazoo :
“The Forestry Department reports no real stand of bur oaks in
this vicinity. Scattered trees are found throughout the city,
perhaps the largest group being that of eight or ten in Bronson
Park. Formerly groves of bur oaks were found near Kalamazoo
including a large stand near Oshtemo on route U. S. 12.”
The total area of the prairies and of the oak openings in
southern Michigan was relatively small in comparison to the
area in southern Wisconsin but evidently the character of the
bur oak openings was quite the same in both regions.
Concluding Remarks. — The early records are particularly
complete and accurate for the main facts regarding the charac¬
ter, location, and extent of the bur oak openings in Wisconsin.
Their relations and ecological status in the so-called oak-hickory
belt which constitutes the western margin of the extensive east¬
ern forests of North America are now well recognized.
For perhaps a hundred years before the advent of the white
settlers into southern Wisconsin the oak opening prairie asso¬
ciation was a somewhat static feature in the midst of a region
where there had been dynamic changes in post-glacial plant mi¬
grations. Both the prairie and the forest are decidedly static
and self-sustaining and the two tend to be mutually exclusive.
In the bur oak openings these two sharply contrasted types of
160 Wisconsin Academy of Sciences , Arts and Letters
vegetation are combined in a somewhat balanced and static re¬
lationship that is indeed noteworthy and of special interest.
But the coming of the white man spelled the doom of the oak
openings. The land they occupied was fertile, there was suffi¬
cient timber for the immediate needs of the settlers, yet the
stands of the trees were so sparse that the clearing involved
relatively little labor. Within fifty years most of the oak open¬
ings were converted into fields of corn, wheat, oats, and tobacco
or were filled in by the second growth which was mostly of in¬
vading black oaks. At the present time, after another fifty
years, there exist only few scattered remnants of the once nu¬
merous bur oak openings. Of these the Babcock grove now occu¬
pies about fifty acres and is still in an excellent state of preser¬
vation. It is the memory of the grandeur and the beauty of the
extensive groves, of which this is a remnant, that has prompted
this epitome which perhaps may be considered an obituary of
the bur oak openings in Wisconsin.
Literature Cited
1. 1846. Wisconsin, its geography and topography. By I. A. Lapham.
2. 1856. History of Rock County. Edited and compiled by Orrin Guernsey
and Josiah F. Willard. Published by the Rock County Agricultural
Society and Mechanics’ Institute, Janesville.
3. 1875. Notes on the Big Woods. By N. H. Winchell, in Annual Rep. State
Hort. Soc.
4. 1877. Geology of Wisconsin, 2: Part 2. By T. C. Chamberlin. The map of
the native vegetation of Wisconsin, Plate No. IIA, bears the date 1882.
5. 1880. History of Dane County, Wisconsin. Western Historical Society.
6. 1884. Report on the forests of North America. By Charles S. Sargent. In
Tenth Census of the United States, Vol. 9.
7. 1892. On the flora of Madison and vicinity. Trans. Wis. Acad. Sci., 9:
45-135. By L. S. Cheney and R. H. True
8. 1892. The metaspermae of the Minnesota valley. By Conway MacMillan.
9. 1895. The silva of North America, Vol. 8. By Charles S. Sargent.
10. 1898. The phytogeography of Nebraska. By Roscoe Pound and Frederic E.
Clements.
11. 1899. Minnesota plant life. By Conway MacMillan.
12. 1907. A botanical survey of the Illinois River Valley sand region. Bull.
HI. State Lab. of Nat. Hist., 7: 149-194. By H. A. Gleason.
13. 1910. The vegetation of the inland deposits of Illinois. Bull. Illinois State
Lab. Nat. Hist., 9: 23-174. By H. A. Gleason.
14. 1923. The vegetational history of the Middle West. Annals Ass’n. Am.
Geographers, 12: 39-85. By H. A. Gleason.
15. 1924. Atlas of American Agriculture, Part I. Section E. By H. L. Shantz
and Raphael Zon.
Stout — Bur Oak Openings in Southern Wisconsin 161
16. 1927. An annotated flora of the Chicago area. Bull. 8. Nat. Hist. Survey.
By H. S. Pepoon
17. 1927. Factors controlling germination and early survival in oaks. Bull.
No. 19, Yale School of Forestry. By Clarence F. Korstian.
18. 1928. Flora of the oak openings west of Toledo. Prod. Ohio Acad. Sci., 8:
81-134. By Edwin L. Moseley.
19. 1932. Root system of Quercus macrocarpa in relation to the invasion of
prairie. Bot. Gazette, 94: 51-85. By J. E. Weaver and Joseph
Kramer.
20. 1938. Plants as soil indicators. Yearbook of U. S. Dept, of Agriculture,
pp. 835-860. By H. L. Shantz.
21. 1940. The steep prairies of southern Wisconsin and their invasion by forest.
By Elizabeth Anna Chavannes. An unpublished thesis in the records
of the University of Wisconsin, loaned to the writer by Prof. N. C.
Fassett. The investigation was financed by the Alumni Research
Foundation of the University of Wisconsin.
22. 1941. Knowing your trees. By C. H. Collingwood.
SOME AQUATIC AND SUB-AQUATIC PLANTS FROM
THE REGION OF GLACIAL LAKE WISCONSIN
John Catenhusen
This paper records some of the aquatic and sub-aquatic
plants occurring on the bed of Glacial Lake Wisconsin (Fig. 1)
and contains notes on rare or interesting species. Of special
interest are several plants of the Atlantic coastal plain which
occur in this region. The remaining species have been listed
here chiefly as a matter of record. Since they are all native to
the region it was deemed worthwhile to record them because of
extensive plantings of aquatic plants (obtained from commercial
seed distributors) by the Resettlement Administration in 1936
and 1937 and in more recent years by the Fish and Wildlife
Service.
Collections were made during the month of August of the
years 1938 to 1940 incidental to a study concerning the bog
vegetation of the region. The study was made possible by grants
from the Alumni Research Foundation of the University of Wis¬
consin. Grateful acknowledgment is made to Professor N. C.
Fassett for many helpful suggestions. All plants collected were
checked against records of plantings made by the organizations
mentioned above to make certain that they were native to the
area. Expressions of relative abundance refer only to their
status in the region.
Glacial Lake Wisconsin was formed by the damming of the
pre-Glacial Wisconsin River by the advancing ice sheet. After
the ice melted away, the lake was drained by the east fork of the
Black River. After the lake was drained, peat bogs formed in
the low places, while red and white pine stands developed on the
interspersed sand islands and sandstone ridges.
About 1900 the entire area was cut through by a network
of drainage ditches. Much of the area was drained completely.
Several severe fires followed the artificial drainage, burning deep
basins into the peat and destroying much of the native vegeta¬
tion. Those aquatic plants which survived occurred in protected
163
164 Wisconsin Academy of Sciences, Arts and Letters
Figure l . -^Clacial^Lake^Wisconsin^
Figure 1. The graph shows the number of tons of lime sold annually from
1904 to 1940 by Wisconsin producers. The solid line indicates the total amount
of lime sold while the two broken lines show the amount sold for the specific
purposes indicated. Note that as the total production declined a smaller
percentage has been sold for building purposes.
cranberry reservoirs or migrated to the artificially constructed
ditches. In 1933 and the years following, dams and dikes were
constructed in an effort to raise the water-table to its original
level. Flowages were created above the dikes, and shallow pools
were formed in the burned-out peat basins. The past few years
C at enhusen— Aquatic and Sub-Aquatic Plants
165
have witnessed an invasion of these pools and flowages by the
aquatics restricted for years to the ditches and cranberry reser¬
voirs.
Typha latifolia L. — Abundant. It easily pioneers exposed, wet
places and shallow pools. In some instances it has taken over
recently impounded flowages.
Sparganium americanum Nutt. — Common, particularly in
creeks.
Sparganium chlorocarpum Rydb.— Common, particularly in
creeks.
POTAMOGETON CAPILLACEUS Poir. — Uncommon. A plant of the
coastal plain (Fernald 1932) which exhibits a range in Wis¬
consin typical of this group of plants. One station is known
in northern Wisconsin in Sawyer County and two stations
occur in Juneau County in this region.
POTAMOGETON epihydrus Raf. var. Nuttallii (C. & S.) Fer¬
nald.— The most abundant of the Potamogetons of this re¬
gion. Many of the ditches and flowages support at least some
individuals.
POTAMOGETON foliosus Raf.— Fairly common, particularly in
some of the creeks of eastern Jackson County.
POTAMOGETON XLLINOENSI3 Morong.— Generally uncommon, but
abundant in one ditch in northern Juneau County.
POTAMOGETON NATANS L. — Uncommon. Restricted to older
flowages and ditches.
POTAMOGETON oakesianus Robbins. — Uncommon. Restricted to
older flowages and ditches.
POTAMOGETON pulcher Tuckerm. — Rare. A plant of the coastal
plain with a range in Wisconsin similar to that of Potamoge-
ton capillaceus. In this region it occurs only in Juneau Coun¬
ty in a cranberry reservoir which is over 40 years old.
POTAMOGETON SPIRILLUS Tuckerm.— Rare. Found in the same
reservoir in which Potamogeton pulcher was found.
Sagittaria cristata Engelm. — -Common on sandy shores of
lakes in southern Adams County.
Sagittaria latifolia Willd.— Common in ditches and shallow
pools. It frequently pioneers exposed, wet places.
Sagittaria latifolia Willd. var. obtusa (Muhl.) Wiegand. —
Similar in habit to the above species and often occurring
with it.
166 Wisconsin Academy of Scierices , Arts and Letters
Sagittaria latifolia Willd. forma gracilis (Pursh) Robinson.
— Fairly common. Many individuals occur which grade into
the true form.
Sagittaria rigida Pursh. — Rare. Only one station was located
— a flowage in northeastern Monroe County.
Alisma plantago-aquatica L. — Common. It requires a habitat
similar to that of Sagittaria latifolia and often pioneers ex¬
posed, wet places.
Alisma plantago-aquatica L. var. parviflorum (Pursh) Far-
well. — Similar in habit to Alisma Plantago-aquatica and oft¬
en found with it.
Anacharis occidentalis (Pursh) Victorin. — Uncommon.
Found in some of the older reservoirs.
Vallisneria AMERICANA Michx. — Uncommon, but locally abun¬
dant in northern Juneau County.
Zizania aquatica L. var. angustifolia Hitchc. — Uncommon.
A few scattered colonies occur along some of the creeks.
Zizania aquatica L. var. interior Fassett. — Uncommon. Fair
stands occur along the Lemon weir River in Juneau County;
in addition, many plantings have been made, some of which
have been successful.
Glyceria CANADENSIS (Michx.) Trin. — Common along shallow
creeks and ditches, and along the shores of flowages.
Glyceria grandis Wats. — Less common than the above species ;
occurs in much the same habitat.
Phragmites communis Trin. — Fairly common. It pioneers
areas similar to those of Typha, but to a lesser degree.
ECHINOCHLOA PUNGENS (Poir.) Rydb. — Fairly common. Mucky
shores of flowages and ditches.
Leersia ORYZOIDES (L.) Schwartz. — Very common. Often occurs
as a monotype along wet shores of flowages or ditches.
Leersia oryzoides (L.) Schwartz forma glabra Eaton. — Less
common than the above species. It is usually a submersed
form.
Calamagrostis canadensis (Michx.) Beauv. — This grass often
dominates many acres of wet peat meadows. It easily in¬
vades burned-over peat areas which are subsequently flooded
to the extent that a wet, mucky soil is exposed.
Phalaris arundinacea L. — Uncommon. Occasionally along
shores of older flowages.
Catenhusen — Aquatic and Sub-Aquatic Plants
167
Dulichium arundinaceum (L.) Britton. — Common, especially
in old cranberry reservoirs in the western half of the region.
Eleocharis obtusa (Willd.) Schultes. — Abundant on wet
ground or in extremely shallow water.
Scirpus CYPERINUS (L.) Kunth var. pelius Fernald. — The most
common member of the sedge family in this region.
Scirpus validus Vahl. — Uncommon. Occurs along the shores of
flowages, often extending well into deeper water.
Carex oligosperma Michx. — Uncommon, locally common. This
plant was at one time so abundant that it provided the raw
material for an extensive weaving industry in this region.
Carex vulpinoidea Michx. — Common in wet meadows.
Calla palustris L. — Uncommon, but abundant in several of the
older cranberry reservoirs.
Lemna minor L. — Common throughout the region.
Lemna TRISULCA L. — Less common than the above species.
Pontederia CORDATA L. — Uncommon. Mucky shores or shallow
water.
JUNCUS balticus Willd. var. LiTTORALis Engelm. — Rare. Sandy
shores.
Juncus effusus L. — Common in wet meadows.
Iris virginica L. var. shrevei (Small) Anderson. — Creeks and
older reservoirs.
Polygonum careyi Olney. — Common on exposed, mucky peat.
Polygonum coccineum Muhl. var. pratincola (Greene) Stan¬
ford. — Common on exposed, mucky peat.
Polygonum natans Eaton forma genuinum Stanford. — Com¬
mon on exposed, mucky peat.
Ceratophyllum demersum L.— Uncommon. Occurs abundant¬
ly in an old cranberry reservoir in northern Juneau County.
Nymphaea odorata Ait. — Fairly common in older ditches and
reservoirs.
Nuphar variegatum Engelm. — Fairly common in older ditches
and reservoirs.
Nasturtium officionale R. Br. — Common in cold creeks, espe¬
cially in Jackson County.
Potentilla palustris (L.) Scop. — Uncommon. Occurs in older
cranberry reservoirs.
Callitriche heterophylla Pursh. — Rare. There are three au¬
thentic stations in Wisconsin: one in eastern Jackson Coun¬
ty, and two in the Baraboo Hills in Sauk County.
168 Wisconsin Academy of Sciences, Arts and Letters
Hypericum canadense L. — Uncommon. Several stations were
found: one in northern Juneau County, and several in east¬
ern Jackson County (McLaughlin 1931).
Hypericum virginicum L. var. fraseri (Spach) Fernald. Com¬
mon on wet, mucky soil or in shallow water.
Viola lanceolata L. — Uncommon. Wet, mucky soil.
Didiplis diandra (Nutt.) Wood forma aquatica (Koehne)
Fassett. — Only one station was found, in an old cranberry
reservoir in northern Juneau County.
Ludwigia palustris (L.) Ell. var. Americana (D. C.) Fern. &
Grisc. — Common on wet, mucky soil.
Ludwigia palustris fL.) Ell. var. Americana (T>. C.) Fern. &
Grisc. forma elongata Fassett. Uncommon. Grows in rela¬
tively deep water.
Ludwigia polycarpa Short and Peter. — Uncommon. Wet, mucky
soil.
Myriophyllum farwellii Morong. — Uncommon. One station
occurs in eastern Jackson County, in an old cranberry reser¬
voir.
Utricularia intermedia Hayne. — Less common than the fol¬
lowing species. Ditches and flowages.
Utricularia vulgaris L. var. Americana Gray. — Common.
Many of the ditches and flowages contain this species.
Cephalanthus occidentalis L. — Uncommon. Common in the
bottom lands of Beaver Creek in northern Juneau County.
Lobelia cardinalis L. — Fairly common in bottom lands of the
Wisconsin and Yellow Rivers.
Megalodonta beckii (Torr.) Greene. — Occasional in flowages
and ditches.
Eupatorium perfoliatum L. — Common in wet meadows.
Aster paniculatus Lam. — Common in wet meadows.
Helianthus giganteus L. — Common in wet meadows.
Bidens frondosa L. — Common in damp or wet meadows, and
along ditch banks.
Bidens comosa (Gray) Wiegand. — Common on wet shores and
ditch banks.
Bidens connata Muhl— Common on wet shores and ditch
banks.
Bidens cernua L. — Common in wet meadows and along ditch
banks.
ClRSlUM muticum Michx. — Common in wet meadows.
Catenhusen — Aquatic and Sub-Aquatic Plants
169
Literature Cited
Fernald, M. L.
1932. The linear-leaved North American species of Potamogeton. Memoirs
of the American Academy of Arts and Sciences, 17: 108-112.
McLaughlin, W. T.
1931. Preliminary reports of the flora of Wisconsin: Hypericaceae. Trans,
of the Wis. Acad, of Sci. 2: 285-287.
THE MOSSES OF WISCONSIN
L. S. Cheney and Richard Evans
The following list of mosses was compiled in part from Mr.
Cheney’s manuscript which was partially complete at the time
of his death on April 10th, 1938, and in part from his herbarium
material. He had planned the list to cover not only his own col¬
lections, but likewise the Wisconsin collections of others. So far
as possible, this plan has been followed in completing his list.
Some of the earlier collections here listed are those of T. J.
Hale, I. A. Lapham, R. H. True, Barnes and True, Cheney and
True, and J. M. Holzinger. Later collections which are included
are those of D. F. Costello, J. T. Curtis, R. S. Nanz, and L. R.
Wilson. The great majority of these collections, particularly the
older ones, are to be found in the Herbarium of the University
of Wisconsin ; some of the later ones are represented only in the
Cheney Herbarium, which has been deposited through the cour¬
tesy of his daughter, Miss Monona L. Cheney, in the University
Herbarium.
In 1893 Cheney in conjunction with R. H. True published
“On the Flora of Madison and Vicinity, a Preliminary Paper on
the Flora of Dane County, Wisconsin” in the Transactions of
the Wisconsin Academy of Sciences, Arts and Letters (9: 45-
135). This list includes three species of Sphagnum and one hun¬
dred thirty-two Eubryales. In 1894 Cheney published in the
same Transactions (10: 66-68) a list of Sphagna collected dur¬
ing the summer of 1893 along the Wisconsin River between Lac
Vieux Desert and Wausau. The identifications were made by
Dr. Carl Warnstorf. These earlier collections are included in the
present list. No attempt at specific mention of collectors has
been made in completing the list, since by far the greatest num¬
ber of the collections were made by Cheney. The portion of his
original manuscript which was completed, in which collectors
and identifying collection numbers were given, is deposited with
his herbarium.
Some few liberties were taken in editing this list. Nomen-
171
172 Wisconsin Academy of Sciences , Arts and Letters
clature has been brought in line as completely as possible with
Grout’s “Moss Flora of North America North of Mexico” and
with Grout’s “List of Mosses of North America North of Mexi¬
co” (Bryologist 43: 117-131, 1940). Nomenclatorial changes in
all cases have been indicated. In a very few cases in which
Cheney left identifications in doubt, material has been reworked,
but in the main identifications have been left as he made them.
It is certain that Mr. Cheney would have expressed his grati¬
tude to various investigators — among them Miss Winona Welch
who checked, seemingly, most of his Fontinalis identifications. It
is unfortunate that others cannot be cited specifically because of
lack of information with respect to their contributions. I should
like to express my own gratitude to Prof. N. C. Fassett of the
University of Wisconsin and to Prof. H. S. Conard of Grinnell
College for aid in solving nomenclatorial puzzles; likewise to
Mr. E. F. Bean, State Geologist, and to Mr. C. E. Brown of the
State Historical Society for aid in identifying obscure or ante¬
dated place names — many of them carried over from old logging
days in the north.
Richard Evans
Department of Botany
The University of Wisconsin
Acaulon
A. RUFESCENS Jaeger. Barron Co. : Barron Twp. Grant Co. :
Glen Haven; Potosi.
Amblyodon
A. DEALBATUS (Hedw.) Beauv. Polk Co.: Osceola.
A. DEALBATUS var. AMERICANUS Ren. & Card. Polk Co. : Osceola.
Amblystegiella
A. confervoides (Brid.) Loeske. Grant Co.: near Bridgeport;
Glen Haven; Lancaster; Pososi; Werley. Jefferson Co.: Pal¬
myra. Lafayette Co.: Fayette. Rock Co.: Beloit; Janesville;
Bradford Twp. Waukesha Co.: Okauchee Lake; Pine Lake.
A. minutissima (Sull. & Lesq.) Nichols. Grant Co.: Glen
Haven ; Potosi.
A. Sprucei (Bruch) Loeske. Ashland Co.: near Ashland on
White River ; Oak Island. Door Co. : Baileys Harbor. Grant
Co.: Glen Haven.
A. subtilis (Hedw.) Loeske. Vilas Co.: Lac Vieux Desert.
Cheney and Evans — The Mosses of Wisconsin 173
Amblystegium
A. compactum (C. Mull.) Aust. Dane Co.: Madison. Grant
Co.: North Andover; Wyalusing. Jefferson Co.: Palmyra.
Rock Co.: Bradford Twp. Trempealeau Co.: Trempealeau
Ridge. Waukesha Co. : Lake LaBelle ; Waukesha.
A. Juratzkanum Schimp. Bayfield Co.: Drummond; LaCha-
pelle (Lashabel’s homestead). Dane Co.: Madison; Blue
Mounds. Grant Co. : Glen Haven. Jefferson Co. : Helenville.
Lafayette Co. : Argyle. Lincoln Co. : Grandfather Falls ;
Grandmother Falls. Oneida Co.: Tomahawk Lake; Whirl¬
pool Rapids. Rock Co. : Beloit ; Bradford Twp. ; Clinton. Vilas
Co. : Conover ; Lac Vieux Desert. Washington Co. : New-
burg. Waukesha Co. : Big Bend ; Lannon ; Oconomowoc ;
Oconomowoc Lake; Pine Lake; Vernon Station; Waukesha.
A. serpens (Hedw.) Bry. Eur. Ashland Co.: Oak Island. Bar¬
ron Co.: Barron. Bayfield Co.: Bayfield; Mason; Orienta;
Port Wing. Dane Co. : Madison. Dodge Co. : Horicon. Doug¬
las Co. : St. Louis River. Grant Co. : Bagley ; Fennimore ;
Glen Haven; Montfort; Wyalusing. Jefferson Co.: Hebron;
Helenville ; Palmyra. Lincoln Co. : NE corner of Co. ; Grand¬
father Falls ; Grandmother Falls. Milwaukee Co. : N. Mil¬
waukee. Oneida Co.: N. central part; McNaughton; Toma¬
hawk Lake. Portage Co. : Stevens Point. Rock Co. : Beloit ;
Bradford Twp.; Clinton; Janesville; Newark Twp. Rusk
Co. : Island Lake ; Strickland. Sauk Co. : Devils Lake. Trem¬
pealeau Co. : Galesville. Vilas Co. : Lac Vieux Desert. Wau¬
kesha Co. : Beaver Lake ; Eagle ; Lannon ; Menomonee Falls ;
Menomonee Twp. ; Mouse Lake ; Mukwonago ; Nashota ; Low¬
er Nashota Lake; Upper Nemahbin Lake; Oconomowoc;
Oconomowoc Lake ; Okauchee Lake ; Pine Lake ; W ales ; Wau¬
kesha.
A. varium (Hedw.) Lindb. Ashland Co.: Manitou Island. Bar¬
ron Co. : Barron. Bayfield Co. : Drummond ; Orienta. Buffalo
Co.: Marshland. Dane Co.: Madison; Verona. Douglas Co.:
St. Louis River. Grant Co.: Bagley; Glen Haven; Patch
Grove ; Potosi. Iowa Co. : Union Mills. Jefferson Co. : Palmy¬
ra ; Sullivan. Kewaunee Co. : Kewaunee. Lincoln Co. : Grand¬
father Falls. Marathon Co.: Granite Heights. Marinette
Co.: Menominee River. Ozaukee Co.: Cedarburg. Polk Co.:
T 37 N R 11 W, near Doran, Burnett Co.; St. Croix Falls.
174 Wisconsin Academy of Sciences , Arts and Letters
Rock Co.: Beloit; Bradford Twp. ; Clinton; Janesville; near
Whitewater. Sheboygan Co.: Cedar Grove; Little Elkhart
Lake. Trempealeau Co. : Trempealeau. Washington Co. :
Newburg. Waukesha Co.: Eagle; Lannon; Upper Lake Ne-
mahbin; North Lake; Oconomowoc; Oconomowoc Lake;
Okauchee Lake; Pewaukee; Pine Lake; Vernon Station;
Wales; Waukesha.
Anacamptodon
A. SPLACHNOIDES (Froehl.) Brid. Barron Co.: Maple Grove
Twp. Grant Co. : Potosi.
Anomodon
A. attenuatus (Hedw.) Huben. Ashland Co.: Penokee Iron
Range. Columbia Co. : Wisconsin Dells. Dane Co. : Blue
Mounds; Madison. Dodge Co.; Roricon. Grant Co.: Glen
Haven ; Potosi. Iron Co. : Montreal River. Lincoln Co. :
Grandmother Falls; Merrill. Milwaukee Co.: S. Milwaukee.
Oneida Co.: McNaughton; Rhinelander. Outagamie Co.:
Appleton; Medina. Ozaukee Co.: Cedarburg. Rock Co.:
Bradford Twp. ; Clinton. Sauk Co. : Devils Lake. Sheboygan
Co.: Cedar Grove; Plymouth. Vilas Co.: Lac Vieux Desert.
Washington Co.: Newburg. Waukesha Co.: Mukwonago;
Waukesha.
A. minor (Beauv.) Lindb. Ashland Co.: Ashland; White River.
Barron Co. : Barron. Bayfield Co. : Drummond ; Port Wing.
Dane Co. : Madison. Dodge Co. : Horicon. Grant Co. : Glen
Haven. Kewaunee Co.: Kewaunee. Lafayette Co.: Fayette.
Lincoln Co. : Grandfather Falls ; Grandmother Falls. Oconto
Co. : Oconto. Outagamie Co. : Appleton. Ozaukee Co. : Cedar¬
burg. Rusk Co. : Murry. Sauk Co. : near Wisconsin Dells.
Sheboygan Co. : Cedar Grove. Waukesha Co. : Waukesha.
A. rostratus (Hedw.) Schimp. Barron Co. : Barron. Dane Co. :
Madison. Dodge Co.: Horicon. Door Co.: Baileys Harbor.
Grant Co.: Glen Haven; Platteville; Potosi. Jefferson Co.:
Helenville; Palmyra. Lincoln Co.: Grandfather Falls. Outa¬
gamie Co.: Appleton. Rock Co.: Bradford Twp.; Clinton.
Rusk Co. : Strickland. Sauk Co. : near Wisconsin Dells.
Washington Co.: Newburg. Waukesha Co.: Eagle; Keesus
Lake ; Nagawicka Lake ; Mouse Lake ; Muskego ; New Berlin ;
Okauchee Lake; Ottawa; Pine Lake; Waukesha.
Cheney and Evans — The Mosses of Wisconsin 175
A. tristis (Cesati) Sull. Barron Co.: Barron. Columbia Co.:
Wisconsin Dells. Grant Co.: Potosi. Lincoln Co.: Grand¬
father Falls; Grandmother Falls. Marathon Co.: Granite
Heights.
A. VITICULOSIS (Hedw.) Hook. & Tayl. Rock Co. : Bradford
Twp. Waukesha Co.: Waukesha.
Aphanorhegma
A. serratum (Hook. & Wils.) Sull. Barron Co.: Barron.
Astomum
A. Muhlenbergianum (Sw.) Grout. Barron Co.: Barron as
A. crispum (Hedw.) Hampe; Barron Co.: Barron as A. Sul-
livantii Sch. ; Dane Co.: Madison as A. Svllivantii Sch. ;
Grant Co. : Potosi as A. Svllivantii Sch.
Atrichum
A. angustatum (Brid.) Bry. Eur. as Catharinea angustata
Brid. Barron Co.: Barron. Bayfield Co.: Drummond. Dane
Co. : Blue Mounds ; Madison ; McFarland. Grant Co. : Werley.
Jefferson Co. : Palmyra. Sauk Co. : Delton. Washington Co. :
Newburg.
A. crispum var. molle (Holz.) Frye as Catharinea mollis Holz.
Buffalo Co. : Marshland.
A. undulatum (Hedw.) Beauv. as Catharine a undulata Web.
& Mohr. Adams Co.: Cold Water Canyon. Ashland Co.:
Basswood Island ; Mellen. Barron Co. : Barron ; Barron
Twp., secs. 20 & 32; Maple Grove Twp., sec. 3. Dane Co.:
Madison. Douglas Co.: Amnicon River; Brule River. Grant
Co. : Glen Haven. Jefferson Co. : Palmyra. Lincoln Co. :
Grandfather Falls ; Tomahawk. Marathon Co. : Granite
Heights ; Mosinee. Oconto Co. : Oconto. Sauk Co. : Baraboo ;
Devils Lake. Vilas Co. : Eagle River ; Star Lake. Waukesha
Co. : Eagle Lake ; Oconomowoc ; Pine Lake ; Waukesha.
Aulacomnxum
A. heterostichum (Hedw.) Bry. Eur. Dane Co.: Blue Mounds.
Grant Co. : Bagley ; Potosi. Lafayette Co. : Fayette.
A. palustre (Web. & Mohr) Schwaegr. Ashland Co.: Odanah;
Basswood Island. Bayfield Co.: Port Wing; Sand Bay. Dane
Co. : Madison. Door Co. : Baileys Harbor. Douglas Co. :
176 Wisconsin Academy of Sciences, Arts and Letters
Brule River. Iron Co. : Montreal River. Jefferson Co. : Lake
Mills. Lincoln Co. : Tomahawk. Outagamie Co. : Appleton.
Ozaukee Co. : Cedarburg. Rock Co. : Newark. Sauk Co. : near
Wisconsin Dells. Vilas Co.: near State Line. Washington
Co. : Newburg. Waukesha Co. : Summit Center ; Sussex ; near
Wales ; Waukesha. Wood Co. : Wisconsin Rapids.
Rarbula
B. acuta (Brid.) Brid. as B. gracilis Schwaegr. Rock Co.:
Avon.
B. CONVOLUTA Hedw. Jefferson Co. : Palmyra. Outagamie Co. :
Seymour. Waukesha Co. : Pine Lake.
Ba fallax Hedw. Bayfield Co.: Mason. Dane Co.: Madison.
Douglas Co. : Amnicon River. Grant Co. : Beetown ; near
Bridgeport; Glen Haven; Mt. Hope; Patch Grove; Potosi;
Werley. Jefferson Co. : Jefferson. Lafayette Co. : Fayette.
Rock Co.: Clinton; Newark. Waukesha Co.: Waukesha.
B. UN GUICULATA Hedw. Dane Co.: Blue Mounds; Madison.
Door Co.: Baileys Harbor. Grant Co.: Glen Haven; Mt
Hope; Potosi. Jefferson Co.: Palmyra. Ozaukee Co.: Cedar
burg. Rock Co. : Beloit ; Bradford Twp. ; Newark. Trempea¬
leau Co.: Trempealeau. Walworth Co.: Whitewater. Wau¬
kesha Co.: Eagle; Glen Cove Station (Pewaukee Lake) ; Me¬
nomonee Falls ; Nashotah ; Waukesha.
Bartramia
B. pomiformis Hedw. Adams Co.: near Wisconsin Dells. Ash¬
land Co. : Basswood Island ; Mellen ; Oak Island ; White Riv¬
er, near Ashland. Barron Co.: Barron; Barron Twp., secs.
5 & 20. Bayfield Co. : Drummond ; Herbster ; Sand Bay. Dane
Co.: Blue Mounds; Madison. Douglas Co.: Amnicon Falls;
Old Superior. Grant Co.: Millville; Patch Grove; Potosi.
Iron Co.: Montreal River. Lincoln Co.: Grandfather Falls;
Tomahawk. Manitowoc Co.: Manitowoc. Milwaukee Co.:
Milwaukee. Oneida Co.: Newbold; Rhinelander. Sauk Co.:
Devils Lake.
Blindia
B. ACUTA (Hedw.) Bry. Eur. Bayfield Co.: Herbster; Houghton
Quarry; Port Wing.
Cheney and Evans — The Mosses of Wisconsin 177
Brachythecium
B. ACUTUM (Mitt.) Sull. Barron Co.: Barron; Barron Twp.,
sec. 32 ; Clinton Twp. Dane Co. : Madison. Grant Co. : Glen
Haven. Jefferson Co.: Palmyra. Outagamie Co.: Appleton.
Ozaukee Co. : Cedarburg. Bock Co. : Clinton ; Newark Twp.
Waukesha Co. : Mukwonago ; Waukesha.
B. campestre Bry. Eur. Bayfield Co. : White River. Iron Co. :
Montreal River, near Lake Superior. Price Co.: Ogema.
Sheboygan Co. : near Cedar Grove.
B. digastrum C. Mull. & Kindb. Bayfield Co.: LaChapelle
(LashabeFs homestead). Dodge Co.: Horicon. Grant Co.:
Glen Haven. Rock Co. : Avon. Sheboygan Co. : Cedar Grove.
B. flagellare (Hedw.) Jennings, as B. plumosum (Sw.) Br.
& Sch. Ashland Co.: Basswood Island; Oak Island. Barron
Co.: Canton. Bayfield Co.: Herbster; Houghten Quarry;
Port Wing ; Sand Bay ; Sand Island. Iron Co. : Montreal Riv¬
er. Juneau Co. : Germantown. Rock Co. : Clinton. Rusk Co. :
Old Murry.
B. FLEXICAULE Ren. & Card. Jefferson Co. : near Palmyra.
B. oxycladon (Brid.) Jaeger & Sauerb. Barron Co.: near Bar¬
ron ; Barron Twp., secs. 20 & 32 ; Maple Grove Twp., sec. 3.
Bayfield Co. : Drummond ; Port Wing. Douglas Co. : near
mouth of Brule River. Grant Co.: near Potosi. Iron Co.:
NW corner, near Lake Superior. Lafayette Co.: Fayette.
Lincoln Co. : Tomahawk. Milwaukee Co. : Lake Park. Oneida
Co. : Tomahawk Lake. Rock Co. : Bradford Twp. ; near Clin¬
ton; near Newark. Sheboygan Co.: near Cedar Grove.
Washington Co. : near Newburg. Waukesha Co. : near Eagle ;
Okauchee Lake ; near Wales ; Waukesha.
B. plumosum (Sw.) Br. & Sch. (cf. B. flagellare)
B. populeum (Hedw.) Bry. Eur. Bayfield Co.: Sand Bay. Dane
Co.: Blue Mounds. Lincoln Co.: Grandfather Falls. Vilas
Co. : Lac Vieux Desert.
B. reflexum (Starke) Bry. Eur. Barron Co.: Barron. Lincoln
Co.: Grandmother Falls. Oneida Co.: Newbold. Sheboygan
Co. : Cedar Grove. Vilas Co. : Lac Vieux Desert.
B. RIVULARE Bry. Eur. Ashland Co.: Oak Island. Barron Co.:
Barron; Barron Twp., sec. 20; Doyle Twp.; Maple Grove
Twp., sec. 3. Clark Co.: Abbotsford. Door Co.: Sister Bay.
Douglas Co. : Amnicon River. Grant Co. : Bagley ; near Cas-
178 Wisconsin Academy of Sciences, Arts and Letters
tie Rock; Potosi. Jefferson Co.: Palmyra. Juneau Co.: near
“Old Dell House”. Oneida Co.: Rhinelander; Tomahawk
Lake. Ozaukee Co.: Cedarburg. Rock Co.: Bradford Twp.
Rusk Co.: Old Murry. Sauk Co.: Devils Lake. Sheboygan
Co.: near Cedar Grove. Waukesha Co.: North Lake; near
Vernon Station ; Waukesha.
B. rutabulum (Hedw.) Bry. Eur. Bayfield Co.: near Herbster.
Dane Co. : near Madison. Door Co. : Europe Bay. Iron Co. :
Montreal River. Oneida Co. : near Tomahawk Lake. Ozaukee
Co.: near Cedarburg. Rusk Co.: near Old Murry. Vilas
Co. : Star Lake.
B. SALEBROSUM (Web. & Mohr) Bry. Eur. Barron Co. : near
Barron; Barron Twp., sec. 20; Maple Grove Twp., sec. 3.
Bayfield Co.: Port Wing. Dane Co.: Hook Lake; Madison.
Douglas Co.: Brule River. Jefferson Co.: near Cambridge.
Lincoln Co.: Grandfather Falls; Grandmother Falls. Mil¬
waukee Co. : Lake Park. Price Co. : near Ogema. Rock Co. :
Clinton. Rusk Co.: Old Murry. Sauk Co.: Parfreys Glen.
Vilas Co.: Eagle River; Lac Vieux Desert. Waukesha Co.:
Eagle; Lannon; Oconomowoc; Okauchee Lake; Pine Lake;
Waukesha.
B. Starkei (Brid.) Bry. Eur. Barron Co.: Barron Twp.; Maple
Grove Twp.; Stanley Twp. Outagamie Co.: Appleton; Me¬
dina. Rusk Co. : Old Murry. Vilas Co. : Conover ; Lac Vieux
Desert.
B. velutinum (Hedw.) Bry. Eur. Barron Co.: Barron Twp.,
sec. 32; Maple Grove Twp., sec. 3. Calumet Co.: Highcliff.
Iron Co.: Montreal River. Lincoln Co.: Grandfather Falls;
Grandmother Falls ; Tomahawk.
Brothera
B. Leana (Sull.) C. Mull. Barron Co.: Barron; Barron Twp.,
secs. 20 & 32. Jefferson Co.: Helenville; Johnson Creek.
Trempealeau Co.: Trempealeau.
Brotherella
B. delicatula (James) Fleisch. Grant Co.: Glen Haven.
B. recurvans (Mx.) Fleisch. Adams Co.: Cold Water Canyon;
Dells of Wisconsin River. Ashland Co.: Basswood Island;
Hermit Island. Barron Co.: Barron. Bayfield Co.: Herb¬
ster; Houghton Quarry; near Bayfield. Door Co.: Baileys
Cheney and Evans — The Mosses of Wisconsin 179
Harbor. Douglas Co. : Lucius Lake ; T 45 N R 15 W. Grant
Co. : Bagley. Iron Co. : Montreal River. Lincoln Co. : Grand¬
father Falls ; Grandmother Falls ; Tomahawk. Marathon
Co. : Granite Heights ; Mosinee. Oneida Co. : Newbold ; Rain¬
bow Rapids ; Rhinelander ; Tomahawk Lake. Outagamie Co. :
Appleton. Ozaukee Co. : Cedarburg. Rusk Co. : Murry. She¬
boygan Co.: Crystal Lake; Oostburg. Vilas Co.: Conover;
Lac Vieux Desert; State Line; Star Lake. Washington Co.:
Newburg. Wood Co.: Wisconsin Rapids.
B. tenuirostris (Schimp.) Broth. Grant Co.: Werley. Rock
Co.: Clinton.
/
Bruchia
B>. flexuosa (Sw.) C. Mull. Trempealeau Co.: Dodge.
B. Sullivantii Aust. Grant Co. : Bagley ; Glen Haven. Wauke¬
sha Co. : Delafield ; Mukwonago ; Summit Center.
Bryhnia
B. graminicolor (Brid.) Grout. Adams Co.: Artists Glen,
Dells of Wisconsin River. Door Co. : Bailey Harbor.
B. NOVAE-ANGLIAE (Sull. & Lesq.) Grout. Adams Co.: Cold Wa¬
ter Canyon, Dells of Wisconsin River. Barron Co.: Barron
Twp., sec. 20 ; Clinton Twp., sec. 26 ; Maple Grove Twp., sec.
3. Bayfield Co.: Bark Bay; Houghton Quarry. Iron Co.:
Montreal River. Lincoln Co.: Grandfather Falls. Oneida
Co. : near Tomahawk Lake. Vilas Co. : Lac Vieux Desert.
Waukesha Co.: Okauchee Lake.
Bryoxiphium
B. norvegicum (Brid.) Mitt. Adams Co.: Witches Gulch, Dells
of Wisconsin River. Columbia Co. : Wisconsin Dells. Juneau
Co.: Lemonweir River. Sauk Co.: Pewits Nest, near Bara-
boo.
Bryum
B. ARGENTEUM (L.) Hedw. Bayfield Co.: Drummond; Orienta.
Dane Co.: Madison. Douglas Co.: T 45 N R 15 W. Grant
Co. : Cassville; Glen Haven; Potosi. Lincoln Co.: Grand¬
father Falls. Marathon Co. : Mosinee. Oneida Co. : Newbold.
Portage Co. : Stevens Point. Rock Co. : Bradford Twp. Wal¬
worth Co.: Whitewater. Waukesha Co.: Saylesville; Wau¬
kesha; near Waukesha; Waukesha Twp., sec. 24.
180 Wisconsin Academy of Sciences , Arts and Letters
B. BIMUM Schreb. cf. B . pseudo triquetrum (Hedw.) Schwaegr.
B. caespiticium (L.) Hedw. Ashland Co.: Basswood Island;
Oak Island; Bayfield Co.: Drummond; Houghten Quarry;
Sand Bay. Burnett Co. : Swiss. Dane Co. : Hook Lake ; Madi¬
son. Grant Co. : Bagley ; Glen Haven ; Potosi ; Williams. La¬
fayette Co.: Argyle. Lincoln Co.: Grandfather Falls; same
station as B. synoico-caespiticium C.M. & Kindb. ; Toma¬
hawk ; Wisconsin River Valley. Polk Co. : near Doran. She¬
boygan Co.: Cedar Grove. Vilas Co.: Lac Vieux Desert.
Washburn Co. : Spooner. Waukesha Co. : Lannon ; Naga-
wicka Lake ; Pewaukee ; Waukesha.
B. capillare (L.) Hedw. Barron Co: Maple Grove Twp., sec.
1. Grant Co. : Mt. Ida. Lincoln Co. : Grandfather Falls as B.
obconicum Hornsch. Oneida Co.: Rhinelander; Tomahawk
Lake. Ozaukee Co. : Cedarburg. Polk Co. : near Doran. Wau¬
kesha Co. : Waukesha. Wood Co. : Wisconsin Rapids, as B.
obconicum Hornsch.
B. cirratum Hoppe & Hornsch. Grant Co. : Montfort. Lincoln
Co. : Tomahawk. Waukesha Co. : Lisbon Twp. ; Waukesha.
B. CUSPIDATUM (Bry. Eur.) Schimp. as B. affine Lindb. Bay-
field Co. : Houghton Quarry ; Sand Island. Grant Co. : Cor¬
nelia; Glen Haven; Potosi. Lincoln Co.: Grandfather Falls;
near Grandfather Falls. Milwaukee Co. : S. Milwaukee.
Waukesha Co. : Lannon ; Lisbon Twp. ; Waukesha.
B. inclinatum (Web. & Mohr) Sturm. Bayfield Co. : Drum¬
mond. Grant Co. : Dickeysville. Lincoln Co. : Grandfather
Falls ; Tomahawk.
B. INTERMEDIUM (Ludw.) Brid. (?) M.F.N.A. 2:229. Grant
Co.: Glen Haven. Iron Co.: Montreal River. Washington
Co. : Newburg. Waukesha Co. : Waukesha.
B. pallens (Web. & Mohr) Brid. Barron Co.: Barron; Doyle
Twp., sec. 28. Grant Co. : Glen Haven ; Jamestown ; Potosi.
Oneida Co.: Rainbow Rapids; near Tomahawk Lake. Ozau¬
kee Co. : Cedarburg. Waukesha Co. : Mukwonago; Waukesha.
B. PENDULUM (Hornsch.) Schimp. Ashland Co.: Basswood Is¬
land. Barron Co.: Cameron; Maple Grove Twp. Bayfield
Co.: Herbster; Port Wing; Siskowitt Bay. Dane Co.: Blue
Mounds; Madison; Marshall; Windsor. Grant Co.: Bagley;
Glen Haven ; Montfort. Iron Co. : Montreal River, near Lake
Superior. Juneau Co. : Dells of Wisconsin River. Lincoln
Cheney and Evans — The Mosses of Wisconsin 181
Co.: Grandfather Falls; near Grandfather Falls. Rock Co.:
Beloit; Bradford Twp. ; Janesville. Sauk Co.: Ironton. She¬
boygan Co. : Cedar Grove. Waukesha Co. : Eagle.
B. PSEUDOTRIQUETRUM (Hedw.) Schwaegr. as B. bimum Schreb.
excepting for those stations marked with an *. These collec¬
tions were listed originally as B. ps endo trique tram . Ashland
Co.: Basswood Island; same station *; Oak Island; White
River. Bayfield Co. : Drummond ; same station * ; Orienta ;
Port Wing; Sand Bay; Siskowitt Bay; Squaw Bay. Door
Co.: Baileys Harbor. Douglas Co.: Amnicon Falls; Manitou
Falls. Grant Co. : Glen Haven ; Potosi. Lincoln Co. : Grand¬
father Falls; same station * ; Merrill *; Tomahawk. Mani¬
towoc Co. : Two Rivers. Oneida Co. : McNaughton ; Newbold ;
Rhinelander * ; Tomahawk Lake. Ozaukee Co. ; Cedarburg.
Polk Co. : near Doran. Portage Co. : Stevens Point. Rock
Co. : Beloit ; Clinton. Rusk Co. : NW corner of county. Wash¬
ington Co.: Newburg. Waukesha Co.: Eagle; North Lake;
Vernon Station; Waukesha; same station *.
B. tortifolium Funck. as B . cyclophyllum Br. & Sch. Bayfield
Co. : Siskowitt Bay. Door Co. : Baileys Harbor.
B. ULIGINOSUM (Brid.) Bry. Eur. Dane Co.: Hook Lake; Lake
Kegonsa. Grant Co.: Patch Grove. Lafayette Co.: Fayette.
Outagamie Co.: Appleton.
B. Weigelii Spreng. as B. Duvalii Voit. Barron Co.: Barron
Twp., secs. 5 & 20 ; Cameron. Oneida Co. : Tomahawk Lake.
Ozaukee Co. : Cedarburg. Vilas Co. : Lac Vieux Desert.
Buxbaumia
B. aphylla Hedw. Vilas Co. : Conover.
Calliergon
C. CORDIFOLIUM (Hedw.) Kindb. Ashland Co.: Ashland; La-
Pointe, Madeline Island. Barron Co. : Barron ; Barron Twp.,
sec. 20 ; Maple Grove Twp., sec. 8. Bayfield Co. : Bark Bay ;
Houghton Quarry; Orienta; Sand Bay. Door Co.: Baileys
Harbor. Douglas Co.: Upper Lucius Lake. Lincoln Co.:
Grandfather Falls; near Grandfather Falls; Merrill. Mara¬
thon Co. : Granite Heights. Oneida Co. : Rhinelander ; Toma¬
hawk Lake. Outagamie Co. : Cedarburg. Portage Co. : near
Stevens Point. Rusk Co. : Strickland. Vilas Co. : near State
Line. Waukesha Co. : Waukesha.
182 Wisconsin Academy of Sciences, Arts and Letters
C. GIGANTEUM (Schimp.) Kindb. Ashland Co.: Mellen. Burnett
Co. : Swiss. Door Co. : Baileys Harbor. Milwaukee Co. : Mil¬
waukee. Outagamie Co. : Appleton. Ozaukee Co. : Cedarburg.
C. Richardsonii (Mitt.) Kindb. Vilas Co.: near Eagle River.
C. stramineum (Brid.) Kindb. Bayfield Co.: Port Wing. Onei¬
da Co.: Newbold. Vilas Co.: Conover; Lac Vieux Desert;
near State Line.
C. trifarium (Web. & Mohr) Kindb. Bayfield Co. : Port Wing.
Calliergonella
C. CUSPEDATA (Brid.) Loeske. Dane Co.: Madison. Ozaukee
Co.: Cedarburg. Waukesha Co.: Mukwonago; Waukesha.
C. Schreberi (Bry. Eur.) Grout. Ashland Co.: LaPointe, Mad¬
eline Island. Barron Co.: Maple Grove Twp., sec. 1. Dane
Co.: Blue Mounds; Madison; Pine Bluff. Grant Co.: Glen
Haven; Mt. Hope. Iron Co.: NW corner of county. Jefferson
Co. : Palmyra. Lafayette Co. : Fayette. Outagamie Co. : Ap¬
pleton. Rock Co.: Bradford Twp.; Newark. Vilas Co.: near
State Line; Conover.
Camptothecium
C. NITENS (Hedw.) Schimp. Ashland Co.: Ashland. Door Co.:
Baileys Harbor. Jefferson Co.: Lake Mills; Palmyra. Ozau¬
kee Co. : Cedarburg. Vilas Co. : Lac Viuex Desert. Waukesha
Co. : Nagawicka Lake ; Mukwonago.
Campylium
C. CHRYSOPHYLLUM (Brid.) Bryhn. Ashland Co.: Oak Island;
White River. Barron Co.: Barron; Maple Grove Twp. Bay-
field Co.: Bayfield; Herbster; Mason; Port Wing; Squaw
Bay. Dane Co.: Mendota. Dodge Co.: Iron Ridge. Douglas
Co. : T 45 N R 15 W. Grant Co. : Bagley ; Glen Haven; James¬
town Twp. Iron Co.: Montreal River. Lincoln Co.: Grand¬
mother Falls ; near Tomahawk. Oneida Co. : near Tomahawk
Lake. Rock Co. : Clinton ; Newark. Sauk Co. : near Baraboo.
Sheboygan Co.: Cedar Grove. Vilas Co.: Lac Vieux Desert;
near State Line. Washington Co. : Newburg. Waukesha Co. :
Lannon; Oconomowoc Lake; Vernon Station.
C. hxspidulum (Brid.) Mitt. Adams Co.: Dells of Wisconsin
River. Ashland Co. : Basswood Island ; Manitou Island ; Oak
Island ; White River. Barron Co. : Barron ; Barron Twp..
Cheney and Evans — The Mosses of Wisconsin 183
secs. 19 and 20; Maple Grove Twp., sec. 3. Bayfield Co.:
Bayfield; Drummond; Houghton Quarry; Port Wing; Sand
Bajr. Dane Co.: Madison. Dodge Co.: Horicon. Door Co.:
Ellison Bay. Douglas Co.: near Superior, T 45 N R 15 W.
Grant Co. : Bagley ; Glen Haven ; Potosi. Iron Co. : Montreal
River; Pence. Jefferson Co.: Palmyra. Lafayette Co.: Fay¬
ette. Lincoln Co.: Grandfather Falls; Merrill. Marathon
Co.: Granite Heights. Oneida Co.: Newbold; Rhinelander;
Tomahawk Lake; Whirlpool Rapids. Rock Co.: Clinton;
Newark. Rusk Co.: Old Murry. Sauk Co.: Devils Lake.
Sheboygan Go.: Cedar Grove. Vilas Co.: Conover; Eagle
River; Lac Vieux Desert. Washington Co.: Newburg. Wau¬
kesha Co.: Mouse Lake; Nashotah Lake; Norris Farm for
Boys; Oconomowoc Lake; Okauchee Lake; Pine Lake.
C. polygamum (Bry. Eur.) Bryhn. Barron Co.: Barron. Bay-
field Co.: Herbster; Sand Bay. Lincoln Co.: Grandfather
Falls; Tomahawk. Oneida Co.: Rhinelander. Outagamie
Co. : Appleton. Sheboygan Co. : Cedar Grove. Waukesha Co. :
Waukesha.
C. stellatum (Hedw.) Lange & C. Jens. Dane Co.: Windsor.
Door Co.: Baileys Harbor. Iron Co.: Montreal River. Jef¬
ferson Co.: Palmyra. Ozaukee Co.: Cedarburg. Waukesha
Co. : Mukwonago ; Waukesha ; near Waukesha.
Ceratodon
C. PURPUREUS (Hedw.) Brid. Ashland Co.: Oak Island. Bay-
field Co.: Houghton; Siskowitt Bay; Squaw Bay. Burnett
Co. : Swiss. Dane Go. : Madison. Dodge Co. : Horicon. Door
Co. : Baileys Harbor. Douglas Co. : Sand Lake ; Winneboujou.
Grant Co. : Potosi. Juneau Co. : Germantown. Milwaukee
Co.: N. Milwaukee. Ozaukee Co.: Thiensville. Rock Co.:
Beloit; Bradford Twp. Sheboygan Co.: Cedar Grove; She¬
boygan. Vilas Co.: Lac Vieux Desert; Star Lake. Washburn
Co.: Spooner. Washington Co.: Newburg. Waukesha Co.:
Lannon ; Menomonee Falls ; Mukwonago ; Oconomowoc ;
Okauchee Lake; Waukesha.
Chamberlainia
C. ACUMINATA (Hedw.) Grout, as Brachythecium acuminatum
(Hedw.) Kindb. Barron Co.: Barron Twp., sec. 20. Dane
Co. : Madison. Grant Co. : Glen Haven ; Mt. Ida Twp. ; Platte-
184 Wisconsin Academy of Sciences , Arts and Letters
ville; Potosi. Lafayette Co.: Fayette. Lincoln Co.: Grand¬
father Falls; Tomahawk. Outagamie Co.: Appleton. Price
Co.: Ogema. Rusk Co.: Murry. Vilas Co.: Conover; Eagle
River. Waukesha Co.: Mukwonago; Okauchee Lake.
C. cyrtophylla (Kindb.) Grout, as Brackythecium cyrtophyl-
lum Kindb. Barron Co. : Barron Twp., sec. 20 ; Maple Grove
Twp. Dane Co.: Blue Mounds; Madison. Grant Co.: Glen
Haven; Patch Grove; Potosi. Oneida Co.: McNaughton.
Outagamie Co. : Greenville. Rusk Co. : near Old Murry. She¬
boygan Co.: near Cedar Grove; Sheboygan. Walworth Co.:
Whitewater. Waukesha Co.: Lake LaBelle; Muskego; Neh-
mabin Lake ; Oconomowoc ; Okauchee Lake ; Pewaukee ; Pine
Lake; near Wales; Waukesha.
Climaceum
C. AMERICANUM Brid. Dane Co.: Blue Mounds; McFarland.
Grant Co. : Beetown ; Bloomington ; Glen Haven ; Platteville ;
Potosi. Lafayette Co. : Fayette. Oconto Co. : Oconto. Rock
Co. : Clinton. Sauk Co. : Devils Lake. Washington Co. : New-
burg. Waukesha Co.: Brookfield Twp.; Menomonee Twp.,
Pine Lake; near Vernon Station; Waukesha.
C. dendroides (Hedw.) Web. & Mohr. Ashland Co.: Penokee
Iron Range. Barron Co.: Barron; Clinton Twp., sec. 26;
Doyle Twp., sec. 38 ; Maple Grove Twp., sec. 3. Bayfield Co. :
Houghton Quarry; LaChapelle, (Lashabel’s Homestead).
Columbia Co. : Wisconsin Dells. Door Co. : Baileys Harbor.
Douglas Co. : Brule River ; Lucius Lake ; SW corner of coun¬
ty. Oneida Co. : Tomahawk Lake. Ozaukee Co. : Cedarburg.
Rusk Co.: Old Murry; Strickland. Sheboygan Co.: Cedar
Grove ; Sheboygan. Vilas Co. : Lac Vieux Desert. Wood Co. :
Nekoosa.
Cratoneuron
C. falcatum (Brid.) Roth. Jefferson Co.: Palmyra. Waukesha
Co. : Big Bend.
C. filicinum (Hedw.) Roth. Dane Co.: Madison. Douglas Co.:
T 45 N R 15 W. Grant Co. : Glen Haven. Iron Co. : Montreal
River. Jefferson Co.: Palmyra. Lincoln Co.: Tomahawk.
Polk Co.: St. Croix Falls. Rock Co.: Newark. Sheboygan
Co. : near Cedar Grove. Vilas Co. : Lac Vieux Desert. Wau¬
kesha Co. : Eagle ; Eagle Lake ; Mukwonago ; Ottawa Twp. ;
Vernon Station; Waukesha.
185
Cheney and Evans — The Mosses of Wisconsin
Desmatodon
D. CERNUUS (Hueben.) Bry. Eur. Waukesha Co.: Waukesha.
D. obtusifolius (Schwaegr.) Jur. as D. arenaceus Sulk Ash¬
land Co.: Basswood Island. Barron Co.: Barron. Bayfield
Co.: Houghton Quarry; Port Wing. Dane Co.: Black Earth;
Madison. Grant Co.: Bagley; Beetown; near Bridgeport;
Glen Haven; Potosi. Jefferson Co.: Lake Koshkonong. La¬
fayette Co.: Fayette. Polk Co.: Osceola. Rock Co.: Avon;
Beloit; Bradford Twp. ; Carvers Rock, Bradford Twp. ;
Janesville. Waukesha Co.: Menomonee Falls.
Dichelyma
D. capillaceum Bry. Eur. Marathon Co.: Granite Heights.
Oneida Co. : Rhinelander. Portage Co. : Stevens Point.
D. falcatum (Hedw.) Myrin. Ashland Co.: Stockton Island
(Presque Isle). Bayfield Co.: Houghton Quarry. Douglas
Co. : shore of Lake Superior near Amnicon River. Lincoln
Co.: Grandfather Falls; Merrill. Marathon Co.: Granite
Heights. Outagamie Co.: Appleton. Rusk Co.: Horseman;
Old Murry.
D. pallescens Bry. Eur. Lincoln Co.: Grandfather Falls.
Oneida Co. : Rhinelander.
Dichodontium
D. pellucidum (Hedw.) Schimp. Ashland Co.: Basswood Is¬
land. Bayfield Co.: Orienta.
D. pellucidum var. fagimontanum (Brid.) Schimp. Iron Co. :
Montreal River, near Lake Superior.
Dicranella
D. cerviculata (Hedw.) Schimp. Bayfield Co.: Houghton
Quarry.
D. heteromalla (Hedw.) Schimp. Adams Co.: near Wisconsin
Dells. Dane Co.: Madison. Grant Co.: Castle Rock. Polk
Co.: St. Croix Falls. Rock Co.: Newark Twp. Waukesha
Co. : New Berlin Twp.
D. humilis Ruthe. Buffalo Co.: Marshland.
D. rufescens (Smith) Schimp. Grant Co.: near Potosi.
D. subulata (Hedw.) Schimp. Bayfield Co.: Houghton Quarry.
D. varia (Hedw.) Schimp. Bayfield Co.: Houghton Quarry.
Dane Co. : Madison. Grant Co. : Bagley ; Glen Haven ; Potosi.
186 Wisconsin Academy of Sciences, Arts and Letters
Lafayette Co.: Fayette. Milwaukee Co.: Milwaukee. Outa¬
gamie Co. : Appleton. Trempealeau Co. : Trempealeau Moun¬
tain, Waukesha Co. : Waukesha.
Dicranum
D. Bergeri Bland. Barron Co.: Barron. Bayfield Co.: Drum¬
mond; Herbster; Port Wing. Buffalo Co.: Marshland. Dane
Co.: Windsor. Door Co.: Baileys Harbor. Green Lake Co.:
Princeton. Jefferson Co.: Lake Mills. Marathon Co.: N. of
Wausau. Oneida Co. : Newbold. Outagamie Co. : Appleton.
Ozaukee Co. : Cedarburg.
D. Bonjeani De Not. Ashland Co. : Basswood Island ; La Pointe,
Madeline Island; Manitou Island; Hermit Island. Bayfield
Co.: Bayfield; Houghton Quarry; Port Wing; Siskowitt Bay.
Dane Co. : Blue Mounds ; Hook Lake as D. Bonjeani var.
Schlotthaueri Barnes ; Madison ; Windsor. Door Co. : Baileys
Harbor. Jefferson Co.: Helenville; Jefferson; Lake Mills;
same station as D. Bonjeani var. juniperi folium Braith. Lin¬
coln Co.: Grandfather Falls; same station as D. Bonjeani
var. Schlotthaueri Barnes ; Merrill. Manitowoc Co. : Two
Rivers. Marathon Co.: near Pine River. Oneida Co.: New-
bold ; Tomahawk Lake ; near Tomahawk Lake. Ozaukee Co. :
Cedarburg. Sauk Co. : Devils Lake. Vilas Co. : Lac Vieux
Desert; near State Line. Waukesha Co.: Beaver Lake; Me¬
nomonee Falls; Mukwonago; Vernon.
D. CONDENSATUM Hedw. Dane Co.: Pine Bluff. Grant Co.:
Castle Rock.
D. Brummondii C. Mull. Ashland Co. : Manitou Island. Barron
Co.: Barron; near Canton. Bayfield Co.: Bark Point; Sand
Bay ; Mason ; Orienta ; Squaw Bay. Dane Co. : Blue Mounds ;
Madison. Door Co. : Baileys Harbor, Douglas Co. : Allouez
Bay; T 45 N R 15 W. Iron Co.: Montreal River. Jefferson
Co. : Palmyra. Lincoln Co. : Grandfather Falls ; Pine River ;
Tomahawk. Oconomowoc Co.: Oconomowoc. Oneida Co.:
Newbold. Vilas Co. : Eagle River.
B. flagellare Hedw. Adams Co.: Cold Water Canyon; Dells
of Wisconsin River. Barron Co. : Barron. Bayfield Co.: Bay-
field ; Mason ; Port Wing ; Sand Bay. Dane Co. : Blue Mounds ;
Madison ; Windsor. Door Co. : Baileys Harbor. Douglas Co. :
Brule River ; Lucius Lake ; T 45 N R 15 W. Grant Co. : Lan¬
caster. Jefferson Co. : Helenville ; Lake Mills. Lafayette Co. :
Cheney and Evans — The Mosses of Wisconsin 187
Fayette. Lincoln Co.: Grandmother Falls. Manitowoc Co.:
Two Rivers. Oneida Co. : Rhinelander ; Tomahaw Lake. Polk
Co.: St. Croix Falls. Sauk Co.: near Wisconsin Dells. She¬
boygan Co. : Cedar Grove ; Sheboygan. Trempealeau Co. :
Trempealeau Mountain. Vilas Go.: Conover; Lac Vieux Des¬
ert ; Sayner. Washburn Co. : Spooner. Washington Co. :
Newburg. Waukesha Co.: Calhoun; Pine Lake. Wood Co.:
Wisconsin Rapids.
D. fulvum Hook. Barron Co. : Barron. Dane Co. : Blue Mounds.
Grant Co. : Castle Rock ; Glen Haven ; near Platteville ; Po-
tosi. Lincoln Co. : Grandfather Falls. Marathon Co. : Granite
Heights. Oneida Co.: Hat Rapids (5 miles N of Whirlpool
Rapids). Sheboygan Co.: Cedar Grove.
D. fuscescens Turn. Ashland Co. : Basswood Island ; LaPointe,
Madeline Island; Hermit Island. Bayfield Co.: Port Wing;
Siskowitt Bay. Dane Co. : Pine Bluff. Door Co. : Baileys
Harbor. Douglas Co. : T 45 N R 1 5 W. Lincoln Co. : Grand¬
father Falls. Oneida Co.: Rhinelander. Vilas Co.: near
State Line.
D. MONTANUM Hedw. Ashland Co. : Hermit Island ; Oak Island.
Barron Co.: Barron. Bayfield Co.: Drummond; Herbster;
Houghton Quarry; Mason; Port Wing. Dane Co.: Madison.
Iron Co. : N W corner, on shore of Lake Superior. Lincoln
Co.: Grandmother Falls; Pine River. Ozaukee Co.: Cedar-
burg. Portage Co. : Stevens Point. Trempealeau Co. : Trem¬
pealeau Mountain. Vilas Co.: Lac Vieux Desert; Sayner.
Waukesha Co.: Okauchee Lake; Pine Lake.
D. Muhlenbeckii Bry. Eur. Dane Co.: Blue Mounds. Lincoln
Co. : Merrill. Sauk Co. : Devils Lake.
D. rugosum (Hoffm.) Brid. Ashland Co.: Basswood Island;
Kakagin River, at Lake Superior; Hermit Island; Long Is¬
land ; Madeline Island ; Odanah. Barron Co. : Barron. Bay-
field Co. : Bark Point ; Drummond ; Houghton Quarry ; Sand
Bay; Sand Island; Siskowitt Bay. Dane Co.: Blue Mounds;
Mendota. Door Co. : Baileys Harbor ; Ellison Bay. Douglas
Co. : T 45 N R 15 w; Lake Superior, near Brule River ; Upper
Lucius Lake, Brule River. Jefferson Co. : Lake Mills. Lin¬
coln Co. : Merrill ; Tomahawk. Manitowoc Co. : Two Rivers.
Oneida Co.: Newbold; Tomahawk Lake. Outagamie Co.:
Appleton. Ozaukee Co.: Cedarburg. Vilas Co.: Eagle River;
State Line. Waukesha Co. : Vernon.
188 Wisconsin Academy of Sciences, Arts and Letters
1), SCOPAEIUM Hedw. Ashland Co. : LaPointe, Madeline Island ;
Oak Island ; Hermit Island. Barron Co. : Prairie Lake Twp.,
sec. 7. Bayfield Co. : Bark Bay ; Drummond ; Plerbster ;
Houghton Quarry; La Chapelle (Lashabel’s homestead) ;
Port Wing; Sand Island; Squaw Bay. Dane Co.: Belleville;
Blue Mounds ; Madison ; near Windsor. Door Co. : near Bai¬
leys Harbor ; Garrett Bay. Douglas Co. : T 45 N R 15 W ;
Brule River; Upper Lucius Lake. Grant Co.: Glen Haven;
Montfort; Werley. Iron Co.: Montreal River. Jefferson Co.:
Lake Mills. Lincoln Co.: Grandmother Falls; Tomahawk.
Marathon Co. : Granite Heights ; near Wausau. Oneida Co. :
near Eagle Lake; Rhinelander; Tomahawk Lake; Whirlpool
Rapids. Ozaukee Co. : Cedarburg. Rusk Co. : Murry ; Strick¬
land. Sauk Co. : Devils Lake. Sheboygan Co. : Cedar Grove ;
Sheboygan. Vilas Co. : Eagle River; Lac Vieux Desert. Wau¬
kesha Co. : Oconomowoc ; Pewaukee ; Pine Lake ; Waukesha
Twp.
D. viride (Sull. & Lesq.) Lindb. Barron Co.: Barron; near
Barron. Bayfield Co. : Bayfield ; Mason. Dane Co. : Madison.
Douglas Co.: near mouth of the Brule River. Grant Co.:
Glen Haven; Mt. Hope; Potosi. Jefferson Co.: Palmyra. La¬
fayette Co. : Fayette. Lincoln Co. : Grandmother Falls ; Mer¬
rill ; Tomahawk. Milwaukee Co. : South Milwaukee. Oneida
Co.: Hat Rapids; McNaughton; Newbold; Rhinelander;
Tomawak Lake. Outagamie Co.: Appleton. Ozaukee Co.:
Cedarburg. Rusk Co. : Strickland. Sauk Co. : near Wisconsin
Dells. Sheboygan Co. : Cedar Grove ; Plymouth. Vilas Co. :
Lac Vieux Desert; near State Line. Washington Co.: New-
burg. Waukesha Co. : Lake Nagawicka ; Nashotah Lake ;
Pine Lake.
Didymodon
D. RECURVIROSTRIS (Hedw.) Jennings as D. rubellus Bry. Eur.
Ashland Co. : Basswood Island ; Manitou Island ; Oak Island ;
near White River. Bayfield Co.: Herbster; Houghton
Quarry; LaChapelle (Lashabel’s homestead); Mason; Port
Wing. Dodge Co. : Horicon. Door Co. : Ellison Bay. Douglas
Co. : T 45 N R 15 W. Grant Co. : Bagley ; Bloomington ; Glen
Haven ; Lancaster ; Millville ; Mt. Hope ; North Andover ;
Patch Grove ; Platteville ; Potosi. Iron Co. : Montreal River.
Lincoln Co.: Grandfather Falls; Grandmother Falls. Mara-
Cheney and Evans — The Mosses of Wisconsin 189
thon Co.: Wausau. Milwaukee Co.: South Milwaukee. Rock
Co. : Beloit ; Carver’s Rock, Bradford Twp. ; Janesville. She¬
boygan Co. : Cedar Grove.
Diphyscium
D. foliosum (Hedw.) Mohr. Columbia Co.: Dells of Wisconsin
River.
Distichium
D. CAPILLACEUM (Hedw.) Bry. Eur. Bayfield Co.: between Port
Wing and Herbster.
D. inclinatum (Hedw.) Bry. Eur. Bayfield Co.: Squaw Bay.
Ditrichum
D. HETEROMALLUM (Hedw.) E. G. Britton, as D. homomallum
Hampe. Jefferson Co.: Palmyra.
D. lineare (Sw.) Lindb. as D. vagina, ns (Sull.) Hpe. Barron
Co.: Maple Grove Twp., sec. 8. Iron Co.: lower Montreal
River.
D. pallidum (Hedw.) Hampe. Adams Co.: Dells of Wisconsin
River. Grant Co. : Bagley ; Glen Haven. Milwaukee Co. : Mil¬
waukee. Rock Go.: Clinton. Sauk Co.: Devils Lake.
D. pusillum (Hedw.) E. G. Britton, as D. tortile Brockm. ex¬
cepting for those stations marked with an *. These collec¬
tions were listed originally as D. 'pusillum. Barron Co. : Bar¬
ron Twp., sec. 26 ; Barron ; Doyle Twp., sec. 33 ; Maple Grove
Twp., sec. 8 ; Prairie Lake Twp., sec. 7. Bayfield Co. : Drum¬
mond. Buffalo Co. : Marshland. Dane Co. : Madison ; same
station *. Iron Co. : Pence. Lincoln Co. : Tomahawk. Mara¬
thon Co. : Granite Heights. Oneida Co. : Noisy Creek ; Rhine¬
lander; Tomahawk Lake. Polk Co.: Osceola. Price Co.:
Ogema. Rock Co. : Newark. Trempealeau Co. : Trempealeau
Mountain *.
Drepanocladus
D. aduncus (Hedw.) Warnst. Dane Co.: Madison. Grant Co.:
Potosi. Waukesha Co.: Eagle; Ottawa Twp.
D. aduncus f. AQUATICUS (Sanio) Monkem. Door Co.: Baileys
Harbor. Jefferson Co. : Palmyra. Sheboygan Co. : Cedar
Grove.
D. aduncus var. Kneiffii (Bry. Eur.) Warnst. Jefferson Co.:
190 Wisconsin Academy of Sciences , Arts and Letters
Ixonia. Manitowoc Co.: Two Rivers. Waukesha Co.: Muk-
wonago ; Okauchee Lake.
D. aduncus var. Kneiffii f. intermedius (B. & S.) Monkem.
Waukesha Co.: Waukesha.
D. aduncus var. Kneiffii f. pseudofluitans (Sanio) Monkem.
Oneida Co. : Tomahawk Lake. Waukesha Co. : Waukesha.
D. aduncus var. polycarpus (Bland.) Warnst. Lincoln Co.:
Tomahawk. Polk Co.: near Doran. Waukesha Co.: Ocono-
mowoc; Vernon; Waukesha.
D. ADUNCUS var. POLYCARPUS f. GRACILESCENS (Bl\ & Sch.)
Monkem. Dane Co. : Blue Mounds. Rock Co. : Newark. Wau¬
kesha Co. : Mukwonago ; Oconomowoc.
D. aduncus var. polycarpus f. uncus Grout. Waukesha Co.:
near Vernon.
D. aduncus var. pseudofluitans f. paternus (Sanio) Grout.
Ashland Co. : Madeline Island. Douglas Co. : mouth of Brule
River.
D. exannulatus (Gumb.) Warnst. Barron Co.: Barron. Onei¬
da Co. : Newbold.
D. exannulatus var. brachydictyus (Ren.) Grout. Oneida
Co. : Tomahawk Lake.
D. exannulatus var. rotae f. falcifolius (Ren.) Grout. Bay-
field Co.: Drummond. Oneida Co.: Tomahawk Lake. Outa¬
gamie Co. : Appleton. Portage Co. : Stevens Point. Vilas Co. :
Weber Lake.
D. fluitans (Hedw.) Warnst. Oneida Co.: Tomahawk Lake.
Vilas Co. : Conover.
D. fluitans f. Jeanbernati (Ren.) Monkem. Barron Co.:
Barron ; Barron Twp., sec. 29. Oneida Co. : Tomahawk Lake.
D. intermedius (Lindb.) Warnst. Door Co.: Baileys Harbor.
Jefferson Co. : Palmyra.
D. revolvens (C. Mull.) Warnst. Door Co.: Baileys Harbor.
Jefferson Co.: Palmyra.
D. Sendtneri (Schimp.) Warnst. Waukesha Co.: Waukesha.
D. Sendtneri f. aristinervis Monkem. Rock Co. : Newark.
D. uncinatus (Hedw.) Warnst. Ashland Co.: Basswood Is¬
land; Hermit Island; Oak Island; near White River. Bay-
field Co.: LaChapelle (LashabePs homestead) ; Mason; Port
Wing; near Port Wing; Sand Bay; Sand Island; Siskowitt
Bay. Dane Co. : Madison. Door Co. : Baileys Harbor. Doug-
Cheney and Evans — The Mosses of Wisconsin
191
las Co.: Amnicon Eiver. Iron Co.: Montreal River. N W
corner of La Pointe Indian Reservation. Lincoln Co. : Grand¬
father Falls ; near Grandfather Falls. Oneida Co. : Toma¬
hawk Lake.
D. UNCINATUS var. PLUMULOSUS (Schimp.) Roth. Door Co.:
Baileys Harbor. Vilas Co.: Lac Vieux Desert. Waukesha
Co. : Big Bend.
D. VERNICOSUS (Lindb.) Warnst. Bayfield Co.: Herbster; Port
Wing. Door Co. : Baileys Harbor. Douglas Co. : T 45 N R 15
W. Lincoln Co. : Tomahawk. Vilas Co. : Conover ; Lac Vieux
Desert; near State Line.
Drummondia
D. prorepens (Hedw.) Jennings as D. clavellata Hook. Barron
Co. : Barron Twp., sec. 20 ; Doyle Twp., sec. 33 ; Maple Grove
Twp. Burnett Co.: Webb Lake. Dane Co.: Madison. Rusk
Co.: Strickland.
Encalypta
E. CILIATA Hedw. Ashland Co.: Manitou Island. Bayfield Co.:
Port Wing. Dane Co. : Blue Mounds. Douglas Co. : T 45 N R
15 W. Grant Co.: Bagley. Iron Co.: Montreal River. Lin¬
coln Co. : Grandfather Falls. Marathon Co. : Wausau. Rusk
Co. : Strickland. Sauk Co. : near Wisconsin Dells.
E. streptocarpa Hedw. Door Co.: Cana Island. Outagamie
Co. : Appleton.
Entodon
E. brevisetus (Hook. & Wils.) Jaeger & Sauerb. Barron Co.:
Barron. Lincoln Co. : Grandfather Falls ; Merrill. Waukesha
Co. : Menomonee Falls.
E. cladorrhizans (Hedw.) C. Mull. Barron Co.: Barron. Dane
Co.: Madison; near Madison. Grant Co.: Glen Haven. Jef¬
ferson Co. : Palmyra ; Sullivan. Lafayette Co. : Fayette.
Outagamie Co. : Appleton. Portage Co. : Stevens Point. Rock
Co.: Clinton. Rusk Co.: Murry. Sauk Co.: near Wisconsin
Dells. Waukesha Co. : Pine Lake ; SaylesviJle.
E. seductrix (Hedw.) C. Mull. Barron Co.: Poskin. Dane Co.:
Madison ; near Madison. Grant Co. : Glen Haven. Jefferson
Co.: Johnson Creek; Palmyra. Portage Co.: Stevens Point.
Rock Co. : Newark Twy. Sheboygan Co.: Franklin. Trem-
192 Wisconsin Academy of Sciences , Arts and Letters
pealeau Co. : Trempealeau Mountain. Waukesha Co. : Ocono-
mowoc; Pine Lake; Waukesha.
Ephemerum
E. COHAERENS (Hedw.) Hampe. Dane Co.: Madison.
E. CRASSINERVIUM (Schwaegr.) C. Miill. Barron Co.: Barron.
Grant Co. : Potosi.
E. spinulosum Schimp. Barron Co.: Barron.
Eurhynchium
E. hians (Hedw.) Jaeger & Sauerb. Dane Co. : Madison. Grant
Co.: Glen Haven; Potosi. Jefferson Co.: Palmyra. Waukesha
Co. : Waukesha.
E. rusciforme (Neck.) Milde. Barron Co.: Campia. Rusk Co.:
Old Murry; sec. 20 T 36 N R 7 W. Sauk Co. : Baraboo.
E. serrulatum (Hedw.) Kindb. Barron Co.: Barron. Dane
Co.: Blue Mounds; Madison. Dodge Co.: Horicon. Grant
Co.: Glen Haven; Lancaster; Werley. Iron Co.: Montreal
River. Jefferson Co.: near Cambridge; Palmyra. Lafayette
Co.: Fayette. Rock Co.: Bradford Twp. ; Newark Twp.
Rusk Co.: Murry. Vilas Co.: Lac Vieux Desert. Waukesha
Co. : Oconomowoc ; Pine Lake.
E. Stokesii (Turn.) Bry. Eur. Outagamie Co.: Appleton.
E. strigosum (Hoffm.) Bry. Eur. Ashland Co.: Hermit Island;
Manitou Island ; Penokee ; White River. Barron Co. : Barron.
Bayfield Co.: Drummond; Herbster; Houghton Quarry; La
Chapelle (Lashabel’s homestead); Mason; Orienta; Port
Wing; Sand Bay. Door Co.: Baileys Harbor. Grant Co.:
Glen Haven ; Patch Grove. Iron Co. : Montreal River, near
Lake Superior. Jefferson Co. : Palmyra. Lincoln Co. : Grand¬
father Falls ; Grandmother Falls ; Merrill ; Tomahawk. Mani¬
towoc Co. : Two Rivers. Oneida Co. : Hat Rapids ; Tomahawk
Lake. Outagamie Co.: Appleton. Price Co.: Ogema. Rusk
Co.: Murry. Sauk Co.: near Wisconsin Dells. Sheboygan
Co. : Cedar Grove. Vilas Co. : Eagle River; Lac Vieux Desert.
Waukesha Co.: North Lake; Okauchee Lake; Pine Lake.
Fabronia
F. ciliaris (Brid.) Brid. as F. octoblepharis (Schleich.)
Schwaegr. Barron Co.: Barron; near Barron. Grant Co.:
Dutch Hollow; Glen Haven; Lancaster; Potosi. Polk Co.:
Cheney and Evans — The Mosses of Wisconsin 193
near Doran. Rusk Co. : Rusk Twp. Waukesha Co. : Ocono-
mowoc.
Fissidens
F. adiantoides Hedw. Barron Co.: Barron. Bayfield Co.:
Houghton Quarry. Dane Co.: Madison. Door Co.: Baileys
Harbor. Iron Co. : Montreal River, near Lake Superior. Lin¬
coln Co. : Grandfather Falls. Outagamie Co. : Appleton.
Waukesha Co.: Vernon; Waukesha.
F. bryoides Hedw. Bayfield Co.: Mason. Dane Co.: Madison;
same station as F, incurvus (Web. & Mohr) Schwaegr.
Douglas Co. : T 45 N R 15 W. Grant Co. : Lancaster ; North
Andover; Potosi. Lincoln Co.: Grandfather Falls; Grand¬
mother Falls ; Merrill. Oneida Co. : McNaughton ; Tomahawk
Lake. Portage Co.: Stevens Point. Washington Co.: New-
burg. Waukesha Co.: Oconomowoc ; Pine Lake, both as F.
incurvus (Web. & Mohr) Schwaegr.
F. cristatus Wils. Adams Co.: Witches Gulch. Ashland Co.:
Basswood Island; White River. Barron Co.: Doyle Twp.
Bayfield Co.: Houghton Quarry; Port Wing. Dane Co.: Blue
Mounds. Door Co. : Baileys Harbor. Grant Co. : Glen Haven ;
Potosi ; Werley. Lafayette Co. : Fayette. Lincoln Co. : Grand¬
father Falls. Milwaukee Co. : South Milwaukee. Oneida Co. :
Hat Rapids; Whirlpool Rapids. Outagamie Co.: Greenville.
Ozaukee Co.: Cedarburg. Rusk Co.: Murry; Strickland.
Washington Co. : Newburg. Waukesha Co. : Menomonee
Falls; Sussex; Vernon; Waukesha.
F. cristatus var. winonensis (Ren. & Card.) Grout. Sauk
Co.: near Wisconsin Dells.
F. exiguus Sull. as F. incurvus var. exiguus Barnes. Ashland
Co.: Basswood Island. Grant Co.: Glen Haven. Milwaukee
Co.: Milwaukee.
F. Julianus (Mont.) Schimp. Barron Co.: Barron. Jefferson
Co.: Palmyra. Portage Co.: Stevens Point.
F. MINUTULUS Sull. The stations marked with an * indicate
collections which were listed as F. incurvus (Web. & Mohr)
Schwaegr. Adams Co. : Cold Water Canyon ; same station *.
Ashland Co. : Basswood Island ; same station *. Barron Co. :
Barron. Grant Co.: Bagley; Fennimore; Glen Haven; same
station * ; Jamestown Twp. * ; Millville ; Mt. Hope ; Mt. Ida ;
North Andover ; Patch Grove ; same station * ; Potosi ; same
i
194 Wisconsin Academy of Sciences , Arts and Letters
station * ; Werley. Lafayette Co.: Fayette; same station *.
Lincoln Co.: Grandfather Falls *. Rock Co.: Beloit; Clinton;
Janesville; same station *. Waukesha Co.: Oconomowoc.
F. obtusifolius Wils. Grant Co.: Bagley; near Bridgeport;
Glen Haven ; Werley.
F. osmundioides Hedw. Ashland Co.: Basswood Island; Oak
Island. Barron Co.: Barron. Door Co.: Baileys Harbor.
Grant Co. : Patch Grove. Lincoln Co. : Merrill. Oneida Co. :
Hat Rapids ; McNaughton ; Tomahawk Lake.
F. Ravenellii Sull. Lafayette Co. : Fayette.
F. SUBBASILARIS Hedw. Waukesha Co.: Waukesha.
F. taxifolius Hedw. Grant Co.: Glen Haven. Lafayette Co.:
Fayette. Rock Co. : Bradford Twp. ; Clinton.
Fontinalis
F. antipyretica Hedw. Ashland Co. : Stockton Island. Barron
Co. : Doyle Twp. Lincoln Co. : Tomahawk. Oneida Co. : Noisy
Creek. Sauk Co.: Baraboo. Vilas Co.: Trout Lake. Wash¬
burn Co. : Minong.
F. ANTIPYRETICA var. gigantea Sull. Ashland Co.: Stockton
Island. Barron Co.: Barron; Campia; Doyle Twp. Douglas
Co.: Amnicon Falls; Solon Springs. Lincoln Co.: Grand¬
father Falls. Manitowoc Co.: Manitowoc. Marathon Co.:
Granite Heights. Oneida Co. : Newbold ; Tomahawk Lake.
Portage Co.: Stevens Point. Rusk Co.: Horseman. Sauk
Co.: Devils Lake. Vilas Co.: Conover; Lac Vieux Desert.
F. dalecarlica Bry. Eur. Marathon Co. : Mosinee.
F. Duriaei Schimp. Barron Co. : Barron ; Doyle Twp. Bayfield
Co. : Drummond. Burnett Co. : Roosevelt Twp. Douglas Co. :
Amnicon Falls; Lucius Lake; T 45 N R 15 W. Jefferson Co. :
Palmyra. Lincoln Co.: Grandfather Falls; Merrill. Oneida
Co.: Hat Rapids; Newbold; Tomahawk; Whirlpool Rapids.
Polk Co.: near Doran. Portage Co.: Stevens Point. Vilas
Co.: Conover; Eagle River; near State Line. Waukesha Co.:
Eagle ; North Lake.
F. FLACCIDA Ren. & Card. Vilas Co. : Trout Lake.
F. hypnoides Hartm. Waukesha Co. : Waukesha.
F. MISSOURICA Card. Barron Co. : Doyle Twp., sec. 33. Lakeland
Twp., Pipe Lake. Lincoln Co. : Merrill as F. Umbachi Card.
F. novae-angliae Sull. Lincoln Co. : Grandfather Falls. Mara¬
thon Co. : Granite Heights.
Cheney and Evans — The Mosses of Wisconsin 195
Funaria
F. AMERICANA Lindb. Grant Co. : Glen Haven. Rock Co. : Brad¬
ford Twp.
F. hygrometrica Hedw. Bayfield Co. : Herbster ; Mason. Dane
Co. : Ellenboro ; Madison. Door Co. : Baileys Harbor. Doug¬
las Co. : T 45 N R 15 W. Grant Co. : Bagley ; Cornelia ; Glen
Haven ; Potosi. Iron Co. : Hurley. Oneida Co. : Noisy Creek ;
Tomahawk Lake. Outagamie Co. : Appleton. Ozaukee Co. :
Cedarburg. Polk Co.: near Doran. Rock Co.: Clinton. She¬
boygan Co.: Sheboygan; Cedar Grove. Vilas Co.: Eagle
River; Lac Vieux Desert; Star Lake. Washington Co.: New-
burg. Waukesha Co. : Menomonee Falls ; Menomonee Twp. ;
Mukwonago; Ottawa Twp.; Saylesville; Vernon Station;
Waukesha. Wood Co.: Wisconsin Rapids.
Grimmia
G. alpicola var. rivularis (Brid.) Broth, as G. apocarpa var.
rivularis Web. & Mohr. Barron Co.: Barron. Bayfield Co.:
Herbster; Houghton Quarry. Lincoln Co.: Grandfather
Falls ; Grandmother Falls ; Merrill. Marathon Co. : Mosinee.
Oneida Co.: Hat Rapids; Rhinelander; Tomahawk Lake.
Portage Co. : Stevens Point. Rusk Co. : Strickland.
G. apocarpa Hedw. Barron Co. : Doyle Twp. Bayfield Co. : Port
Wing. Dane Co. : Blue Mounds ; Madison. Door Co. : Baileys
Harbor. Grant Co.: Glen Haven; Potosi; Wyalusing. Iron
Co. : Montreal River, near Lake Superior. Lincoln Co. :
Grandfather Falls; Grandmother Falls. Oneida Co.: Noisy
Creek ; Rhinelander ; Tomahawk Lake. Outagamie Co. : Ap¬
pleton. Ozaukee Co. : Cedarburg. Rock Co. : Bradford Twp. ;
Clinton; Janesville. Washington Co.: Newburg. Waukesha
Co. : North Lake.
G. apocarpa var. ambigua (Sull.) Jones. Jefferson Co.: Pal¬
myra.
G. apocarpa var. conferta (Funck) Spreng. Dane Co.: Madi¬
son. Door Co.: Cana Island. Grant Co.: Glen Haven; Wer-
ley. Trempealeau Co.: Trempealeau Mountain.
G. apocarpa var. gracilis (Schleich.) Web. & Mohr. Grant
Co. : Glen Haven.
G. calyptrata Hook. Douglas Co. : Manitou Falls.
G. COMMUTATA Huben. Ashland Co.: Basswood Island.
196 Wisconsin Academy of Sciences , Arts and Letters
G. Doniana Smith. Dane Co. : near Madison. Grant Co. : near
Potosi.
G. laevigata (Brid.) Brid. Dane Co.: Madison. Rock Co.:
Bradford Twp. ; Newark Twp.
G. Olneyi Sull. Dane Co. : near Madison.
G. pilifera Beauv. Bayfield Co.: Houghton Quarry; Mason.
Dane Co. : Blue Mounds. Grant Co. : Platteville ; Potosi. Lin¬
coln Co. : Grandfather Falls. Marathon Co. : Mosinee. Onei¬
da Co. : Tomahawk Lake.
G. plagiopodia Hedw. Dane Co.: near Madison. Grant Co.:
Glen Haven ; Potosi.
G. PULVINATA (Hedw.) Smith. Dane Co.: near Madison.
G. teretinervis Limpr. Trempealeau Co. : Trempealeau.
Gymnostomum
G. calcareum Nees & Hornsch. Ashland Co. : Basswood Island.
Bayfield Co. : Herbster ; Houghton Quarry. Dane Co. : Madi¬
son. Douglas Co. : Falls of the Black River. Grant Co. : Bag-
ley; Beetown; near Bridgeport; Cassville; Castle Rock; Glen
Haven; Mt. Hope; North Andover; Potosi. Lafayette Co.:
Fayette. Rock Co.: Beloit; Bradford Twp.; Janesville.
G. RECURVIROSTRUM Hedw. as G. curvirostre (Ehrh.) Hedw.
Bayfield Co.: Port Wing; Squaw Bay. Columbia Co.: Wis¬
consin Dells. Dane Co.: Madison. Grant Co.: Burton; Glen
Haven; Mt. Hope; Platteville; Wyalusing. Iron Co.: Mon¬
treal River, near Lake Superior. Rock Co.: Bradford Twp.
Haplohymenium
H. triste (Cesati) Kindb. cf. Anomodon tristis (Cesati) Sull.
Hedwigia
H. ciliata (Ehrh.) Hedw. Adams Co.: Dells of the Wisconsin
River. Bayfield Co.: Drummond; Houghton Quarry. Dane
Co.: Madison. Douglas Co.: Superior. Grant Co.: Potosi.
Jefferson Co. : Palmyra. Marathon Co. : Wausau. Milwaukee
Co. : South Milwaukee. Outagamie Co. : Appleton. Rock Co. :
Fairfield. Sheboygan Co.: Little Elkhart Lake. Vilas Co.:
Lac Vieux Desert. Waukesha Co. : Brookfield Twp. ; Ocono-
mowoc ; Waukesha.
H. ciliata f. detonsa (Howe) Grout. Ashland Co.: Basswood
Island.
Cheney and Evans — The Mosses of Wisconsin 197
H. ciliata f. viridis (Bry. Eur.) Grout. Dane Co.: near Madi-
ison. Sheboygan Co. : Little Elkhart Lake.
Helodium
H. Blandowii (Web. & Mohr) Warnst. Jefferson Co.: near
Palmyra. Ozaukee Co. : Cedarburg Swamp. Washington Co. :
Newburg. Waukesha Co.: Mukwonago; sec. 33, T 5 N R
18 E.
Heterophyllium
H. Haldanianum (Grev.) Kindb. as Hypnum Haldanianum
Grev. Adams Co.: Cold Water Canyon. Ashland Co.: Oak
Island. Barron Co.: Barron. Bayfield Co.: Drummond;
Herbster; La Chapelle (LashabeFs homestead). Dane Co.:
Madison; Pine Bluff. Door Co.: Sister Bay. Douglas Co.:
Superior ; Brule River ; Upper Lucius Lake. Grant Co. : Glen
Haven. Iron Co.: Montreal River, near Lake Superior. Jef¬
ferson Co. : Helenville ; Lake Mills ; Sullivan. Lafayette Co. :
Fayette. Lincoln Co.: Grandfather Falls; Grandmother
Falls; Pine Islands, near Tomahawk; Tomahawk. Oneida
Co.: Newbold; Rhinelander; Wisconsin River, ten miles be¬
low Eagle River. Price Co. : Knox Mills. Sauk Co. : Baraboo.
Sheboygan Co.: Cedar Grove; Oostburg; Sheboygan. Vilas
Co.: Lac Vieux Desert; near State Line. Waukesha Co.:
Eagle Lake ; Pine Lake. Wood Co. : Wisconsin Rapids.
Homalia
H. Jamesii Schimp. Adams Co. : Cold Water Canyon. Bayfield
Co. : Houghton Quarry. Lincoln Co. : Grandfather Falls.
Marathon Co.: Goodrich Junction; Granite Heights. Oneida
Go. : Hat Rapids. Sauk Co. : Parfreys Glen, near Baraboo.
Homalotheciella
H. subcapillata (Pledw.) Card. Barron Co.: Barron. Grant
Co. : Glen Haven. Oneida Co. : Tomahawk Lake.
Homomallium
H. adnatum (Hedw.) Broth. Barron Co.: Canton; Doyle Twp.
Chippewa Co. : Long Lake. Dane Co. : Blue Mounds ; Madi¬
son. Dodge Co.: Horicon. Grant Co.: Bagley; Glen Haven;
Potosi. Jefferson Co. : Helenville ; Johnson Creek ; Palmyra ;
198 Wisconsin Academy of Sciences , Arts and Letters
Sullivan. Lafayette Co.: Fayette. Milwaukee Co.: Milwau¬
kee. Outagamie Co. : Binghampton Bog, near Appleton. Polk
Co. : St. Croix Falls. Rock Co. : Avon Twp. ; Bradford Twp. ;
Carver's Rocks. Sauk Co.: Devils Lake. Sheboygan Co.:
Cedar Grove. Waukesha Co. : Menomonee Falls ; North Lake ;
Okauchee Lake; Pine Lake; Vernon; Wales; Waukesha.
Hygroamblystegium
H. FLUVIATILE (Hedw.) Loeske. Ashland Co.: Stockton Island;
White River. Barron Co.: sec. 12 T 35 N R 10 W ; Canton;
sec. 8, Maple Grove Twp. Bayfield Co. : Buffalo Bay ; Drum¬
mond; Mason; Port Wing; Siskowitt Bay. Douglas Co.:
Brule River. Grant Co.: Glen Haven; Potosi. Iowa Co.:
Union Mills. Iron Co. : Montreal River. Lincoln Co. : N E
corner; Grandfather Falls. Marathon Co.: Granite Heights.
Oneida Co. : Rhinelander ; ten miles S of Rhinelander ; Toma¬
hawk Lake. Portage Co. : Stevens Point. Rusk Co. : Murry ;
Strickland. Sauk Co. : Baraboo.
H. FLUVIATILE var. OVATUM Grout. Clark Co. : Abbotsford.
H. IRRIGUUM (Wils.) Loeske. Ashland Co.: White River. Bar¬
ron Co. : Barron. Bayfield Co. : Drummond ; La Chapelle
(Lashabel’s homestead) ; Port Wing. Dane Co. : Blue
Mounds ; Madison ; Middleton. Douglas Co. : T 45 N R 15 W ;
Superior. Grant Co. : near Bridgeport ; Glen Haven ; Potosi ;
Wyalusing. Iron Co.: Montreal River, near Lake Superior.
Jefferson Co.: Palmyra. Lincoln Co.: Grandfather Falls.
Milwaukee Co. : Greenfield Twp. ; Milwaukee. Oneida Co. :
Rhinelander. Polk Co. : near Doran. Portage Co. : Stevens
Point. Rock Co.: Beloit; Bradford Twp.; Clinton; Janes¬
ville. Sauk Co.: Devils Lake. Sheboygan Co.: Cedar Grove.
Waukesha Co.: Beaver Lake; Big Bend; Eagle; Lake La-
Belle; Lannon; Lisbon Twp.; Mukwonago; Upper Nemahbin
Lake; Norris Farm for Boys; North Lake; Oconomowoc;
Oconomowoc Lake; Okauchee Lake; Ottawa Twp.; Pewau-
kee; Pine Lake; Sawtelle; Vernon Station; Wales; Wauke¬
sha ; Waukesha Twp.
H. irriguum var. spinifolium (Schimp.) Grout. Ozaukee Co.:
Thiensville. Rock Co.: Clinton.
H. NOTEROPHILUM (Sull.) Warnst. Dane Co.: Madison; Pheas¬
ant Branch; Lake Wingra. Grant Co.: Beet own ; Castle
Rock; Millville; Platteville; Potosi; Wyalusing. Green Lake
Cheney and Evans— The Mosses of Wisconsin 199
Co.: Green Lake. Rock Co.: Clinton; Fairfield. Waukesha
Co.: Eagle; Ottawa Twp.
H. ORTHOCLADON (Beauv.) Grout. Mr. Cheney prefers referring
this plant to a form of H. irriguum : “Dr. Grout makes this
form a sub-species of H. irriguum , but says that it might
better be ranked as a varietal form. My own observations of
a large large number of specimens leads me to place it in the
latter rank. My own series of specimens shows an unbroken
gradation from typical H. irriguum to the extreme forms re¬
ferred to H . irriguum , orthocladon”. Ashland Co.: White
River; Ashland. Iron Co.: Montreal River near Lake Su¬
perior. Lafayette Co. : Fayette. Polk Co. : near Doran. Wal¬
worth Co.: Whitewater. Waukesha Co.: Okauchee Lake;
Waukesha.
Hygrohypnum
H. eugyrium (Bry. Eur.) Loeske. Oneida Co.: Tomahawk
Lake.
H. ochraceum (Turn.) Loeske. Ashland Co.: White River.
Bayfield Co.: Houghton Quarry; Squaw Bay.
H. palustre (Hedw.) Loeske. Ashland Co.: Basswood Island;
shore of Lake Superior; Oak Island; White River. Bayfield
Co.: Herbster; Houghton Quarry; Port Wing; Sand Bay;
Sand Island; Squaw Bay.
Hylocomium
H. splendens (Hedw.) Bry. Eur. as H. yroliferum Lindb. Ash¬
land Co.: Basswood Island; Mellen; White River. Barron
Co.: Barron. Bayfield Co.: Bark Bay; Drummond; Herb¬
ster. Burnett Co. : Swiss ; St. Croix River. Door Co. : Baileys
Harbor. Douglas Co.: Brule River. Manitowoc Co.: Mani¬
towoc. Oneida Co.: Tomahawk Lake. Outagamie Co.: Ap¬
pleton. Ozaukee Co.: Cedarburg. Sheboygan Co.: Cedar
Grove. Vilas Co. : Lac Vieux Desert ; Star Lake.
Hypnum
H. CRISTA-castrensis Hedw. Ashland Co.: Mellen; White Riv¬
er ; Hermit Island. Barron Co. : Barron. Bayfield Co. : Port
Wing; Sand Bay. Dane Co.: Madison. Douglas Co.: T 45
N R 15 W ; Winneboujou. Grant Co. : Glen Haven. Iron Co. :
Montreal River, near Lake Superior ; La Pointe Indian Reser-
200 Wisconsin Academy of Sciences , Arts and Letters
vation. Jackson Co.: Black River Falls. Jefferson Co.: Lake
Mills. Manitowoc Co.: Two Rivers. Oneida Co.: Rainbow
Rapids. Rusk Co. : Murry. Sauk Co. : Baxters Hollow, Bara-
boo Hills. Vilas Co.: Lac Vieux Desert; Conover.
H. cupressiforme Hedw. Grant Co.: Glen Haven; Mt. Hope.
Iron Co. : Montreal River, near Lake Superior.
H. CUPRESSIFORME var. ericetorum Bry. Eur. Bayfield Co.:
Sand Island.
H. CUPRESSIFORME var. filiforme Brid. Bayfield Co. : Houghton
Quarry. Lincoln Co.: Grandfather Falls.
H. curvifolium Hedw. Barron Co.: Barron. Columbia Co.:
Dells of the Wisconsin River. Lafayette Co. : Fayette. Outa¬
gamie Co. : Greenville. Sheboygan Co. : Cedar Grove.
H. fertile Sendt. Bayfield Co. : Herbster ; Sand Bay. Douglas
Co. : T 45 N R 15 W. Iron Co. : Montreal River, near Lake
Superior. Lincoln Co. : Grandfather Falls. Oneida Co. : Rain¬
bow Rapids ; Rhinelander.
H. imponens Hedw. Adams Co. : Dells of the Wisconsin River.
Ashland Co. : Hermit Island ; Oak Island. Barron Co. : Bar¬
ron. Bayfield Co.: Drummond; Herbster; Mason; Squaw
Bay. Dane Co. : Hook Lake. Door Co. : Baileys Harbor.
Douglas Co. : Brule River ; T 45 N R 15 W. Grant Co. : Glen
Haven. Jefferson Co. : Lake Mills. Lincoln Co. : Grandmother
Falls ; near Grandmother Falls. Manitowoc Co. : Two Rivers.
Oneida Co.: McNaughton; Newbold; 8 miles N of Rhine¬
lander. Rusk Co.: Little Falls, Flambeau River. Sheboygan
Co. : Cedar Grove ; Sheboygan. Vilas Co. : Lac Vieux Desert.
H. Patientiae Lindb. as H. arcuatum Lindb. Adams Co. : Cold
Water Canyon, Dells of the Wisconsin River. Barron Co.:
Barron. Bayfield Co.: Houghton Quarry; La Chapelle (Lash-
abel’s homestead) ; Port Wing; Sand Bay. Dane Co.: Madi¬
son. Grant Co. : Bagley. Iron Co. : Montreal River, near Lake
Superior. Jefferson Co.: Helen ville; Palmyra. Lincoln Co.:
Grandfather Falls ; Pine River ; Tomahawk. Marathon Co. :
Granite Heights. Oneida Co.: McNaughton; Noisy Creek;
Rhinelander; Whirlpool Rapids. Ozaukee Co.: Cedarburg.
Polk Co. : near Doran. Racine Co. : Racine. Rock Co. : New¬
ark Twp. Sheboygan Co.: Cedar Grove. Vilas Co.: Eagle
River; Lac Vieux Desert. Washington Co.: Newburg. Wau¬
kesha Co. : Eagle ; Lannon ; Nashotah Lake ; Oconomowoc
Cheney and Evans — The Mosses of Wisconsin 201
Lake; Okauchee Lake; Ottawa Twp. ; Vernon Station; Wau¬
kesha.
H. Patientiae var. elatum S chimp, as H. arcuatum var. ela-
tum Schimp. Rock Co.: Clinton.
H. pratense Koch. Ashland Co. : Basswood Island. Barron Co. :
Barron. Bayfield Co.: Orienta; Port Wing; Sand Bay. Onei¬
da Co. : Hat Rapids ; Noisy Creek ; Rhinelander ; near Rhine¬
lander; Whirlpool Rapids. Vilas Co.: Conover; Lac Vieux
Desert; near State Line. Waukesha Co.: Pine Lake; Vernon
Station ; Waukesha. Waupaca Co. : Readfield.
H. reptile Mx. Ashland Co. : Basswood Island ; Hermit Island ;
La Pointe, Madeline Island ; White River. Barron Co. ; Bar¬
ron. Bayfield Co. : Drummond ; Herbster ; Houghton Quarry.
Chippewa Co. : Long Lake. Dane Co. : Madison ; Mendota ;
Pine Bluff. Douglas Co. : St. Louis River ; Superior. Grant
Co.: Castle Rock; Glen Haven. Iron Co.: Montreal River,
near Lake Superior ; Pence. Lafayette Co. : Fayette. Lincoln
Co.: Grandmother Falls; near Grandmother Falls; Toma¬
hawk. Oneida Co.: Rhinelander; Tomahawk Lake. Outo-
gamie Co. : Medina. Rock Co. : Bradford Twp. ; Clinton.
Rusk Co.: Strickland. Sheboygan Co.: Cedar Grove. Vilas
Co.: Lac Vieux Desert; Sayner. Waukesha Co.: Okauchee
Lake; Pine Lake; Vernon; Wales.
Leptobryum
L. pyriforme (Hedw.) Schimp. Ashland Co.: Basswood Island.
Bayfield Co.: Drummond; Mason; Port Wing. Dane Co.:
Madison. Douglas Co. : near Burnett Co. line ; T 45 N R 15
W. Grant Co. : Potosi. Lincoln Co. : Grandfather Falls.
Oneida Co. : Newbold ; Rainbow Rapids ; Rhinelander. Outa¬
gamie Co. : West Center. Rock Co. : Beloit. Vilas Co. : Con¬
over; near State Line. Waukesha Co.: Lannon; Menomonee
Falls ; Waukesha. Wood Co. : Wisconsin Rapids.
Leptodictyum
L. riparium (Hedw.) Warnst. Ashland Co.: Ashland. Barron
Co.: Maple Grove Twp. Bayfield Co.: Orienta; Drummond.
Dane Co. : McFarland ; Madison ; Pine Bluff. Dodge Co. : Iron
Ridge. Douglas Co.: St. Louis River; Superior. Grant Co.:
Mt. Hope; Platteville; Potosi. Jefferson Co.: Palmyra. Ke¬
waunee Co.: Kewaunee. Lincoln Co.: Grandfather Falls;
202 Wisconsin Academy of Sciences , Arts and Letters
Merrill. Marathon Co. : Granite Heights. Milwaukee Co. :
West Allis. Oneida Co.: Noisy Creek; Wisconsin River.
Price Co.: Knox Mills. Portage Co.: Stevens Point. Rusk
Co. : Wilkinson Twp. Sheboygan Co. : Sheboygan. Vilas Co. :
Eagle River; Lac Vieux Desert. Waukesha Co.: Big Bend;
Lake La Belle; Mukwonago Twp.; Oconomowoc Lake; Ver¬
non Station ; Wales ; Waukesha.
L. riparium f. fluitans (L. & J.) Grout. Grant Co.: Bagley;
Mt. Hope. Oneida Co. : Rainbow Rapids. Ozaukee Co. : Cedar-
burg.
L. RIPARIUM f. flaccidum (L. & J.) Grout. Dane Co.: Madison.
Portage Co. : Stevens Point.
L. RIPARIUM f. longifolium (Schultz) Grout. Portage Co.:
Stevens Point.
L. trichopodium (Schultz) Warnst. Door Co.: Ellison Bay.
Grant Co.: Bagley; Glen Haven. Lincoln Co.: Grandfather
Falls. Oneida Co. : Rhinelander. Sheboygan Co. : Cedar
Grove.
L. vacillans (Sull.) Broth. Douglas Co.: West Superior. Jef¬
ferson Co.: Jefferson; Rome.
Leptodon
L. OHIOENSIS Sull. as Foy'sstroemia ohioensis Lindb. Grant Co. :
Potosi.
Leskea
L. arenicola Best. Grant Co.: Cassville; Glen Haven. Wau¬
kesha Co. : Pine Lake ; Waukesha.
L. gracilescens Hedw. Barron Co.: Barron. Grant Co.: Glen
Haven. Jefferson Co.: Milford; Palmyra Rock Co.: Brad¬
ford Twp.; Carver’s Rocks; Clinton; Janesville. Walworth
Co.: Whitewater. Waukesha Co.: Nemahbin Lake; Ocono¬
mowoc; Oconomowoc Lake; Okauchee Lake; Pine Lake;
Waukesha.
L. NERVOSA (Schwaegr.) Myrin. Ashland Co.: Hermit Island;
Oak Island. Bayfield Co. : Port Wing. Door Co. : Ellison Bay.
Iron Co. : Montreal River, near Lake Superior. Vilas Co. :
Lac Vieux Desert. Waukesha Co. : Oconomowoc.
L. obscura Hedw. Adams Co.: Dells of the Wisconsin River.
Bayfield Co.: Mason. Dane Co.: Madison. Grant Co.: Glen
Haven; Wyalusing. Iowa Co.: Arena. Jefferson Co.: Lake
Cheney and Evans — The Mosses of Wisconsin
203
Koshkonong ; Palmyra. Lincoln Co.: Grandfather Falls;
Grandmother Falls. Marathon Co.: Mosinee. Oneida Co.:
Hat Rapids. Rock Co.: Afton; Beloit; Bradford Twp. ;
Janesville; Newark Twp. Walworth Co.: Whitewater. Wau¬
kesha Co.: Glen Cove Station; Lake La Belle; Waukesha.
L. polycarpa Hedw. Barron Co.: Barron. Bayfield Co.: near
the White River. Dane Co.: Madison. Grant Co.: Glen
Haven; Wyalusing. Iron Co.: Montreal River, near Lake
Superior. Lafayette Co. : Fayette. Lincoln Co. : Grandmother
Falls ; Pine River. Marathon Co. : Granite Heights ; Mosinee ;
Wausau. Oneida Co. : near Eagle River ; McNaughton ; New-
bold ; Rainbow Rapids. Price Co. : Knox Mills.
L. polycarpa var. paludosa (Hedw.) Schimp. Barron Co.:
Barron. Grant Co.: Glen Haven; Platteville. Lincoln Co.:
Grandmother Falls. Oneida Co.: between Eagle River and
Tomahawk Lake. Rock Co. : Beloit.
Leucobryum
L. GLAUCUM (Hedw.) Schimp. Adams Co.: Dells of the Wiscon¬
sin River. Ashland Co. : Basswood Island ; Long Island ; Mel-
len ; Odanah. Barron Co. : Barron. Bayfield Co. : Bayfield ;
Drummond. Dane Co. : Blue Mounds ; Madison. Douglas Co. :
Winneboujou. Grant Co.: Glen Haven; Mt. Hope; Potosi.
Jefferson Co. : Palmyra. Lafayette Co. : Fayette. Lincoln
Co.: Merrill. Outagamie Co.: Medina. Ozaukee Co.: Cedar-
burg. Rock Co. : Newark Twp. Sheboygan Co. : Cedar Grove.
Vilas Co. : Lac Vieux Desert ; near State Line. Washington
Co.: Newburg. Waukesha Co.: Brookfield Twp.; Pine Lake.
Wood Co.: Wisconsin Rapids.
Leucodon
L. brachypus Brid. Iron Co.: shore of Lake Superior, near
Montreal River. Lincoln Co.: Grandfather Falls; Grand¬
mother Falls ; Merrill. Marathon Co. : Granite Heights ;
Wausau. Oneida Co. : Newbold ; near Rainbow Rapids.
L. julaceus (Hedw.) Sull. Grant Co.: Cassville; Glen Haven;
Potosi. Rock Co. : Bradford Twp.
L. sciuroides (Hedw.) Schwaegr. Barron Co.: Barron; Barron
Twp., sec. 20.; Canton; Sumner Twp. Bayfield Co.: Bark
Bay ; Drummond ; Mason. Dane Co. : Blue Mounds. Douglas
Co. : T 45 N R 15 W. Grant Co. : Glen Haven ; Potosi. Jeffer-
204 Wisconsin Academy of Sciences , Arts and Letters
son Co.: Helenville; Jefferson. Oneida Co.: Whirlpool Rap¬
ids. Outagamie Co.: Greenville. Sauk Co.: Devils Lake.
Vilas Co. : Lac Vieux Desert. Waukesha Co : Pine Lake.
Lindbergia
L. BRACHYPTERA var. Austinii (Sull.) Grout. Ashland Co.: Oak
Island. Barron Co. : Barron ; Barron Twp. Dane Co. : Madi¬
son. Grant Co. : Glen Haven ; Platteville ; Potosi. Jefferson
Co. : Milford. Portage Co. : Stevens Point. Rock Co. : Brad¬
ford Twp. ; Clinton. Rusk Co. : Horseman. Vilas Co. : Con¬
over; Lac Vieux Desert. Walworth Co.: Whitewater. Wau¬
kesha Co. : Lake La Belle ; Mouse Lake ; Oconomowoc Lake ;
Pine Lake; Vernon Station; Waukesha.
Meesia
M. triquetra (Hook. & Tayl.) Angstr. Bayfield Co.: Drum¬
mond. Ozaukee Co. : Cedarburg. Vilas Co. : near State Line.
M. uliginosa Hedw. Bayfield Co.: between Herbster and Port
Wing.
Mnium
M. affine Bland. Adams Co.: Dells of the Wisconsin River.
Barron Co.: Barron as M. affine var. ciliare (Grev.) C. M.
Bayfield Co. : Drummond. Calumet Co. : near Menasha.
Dane Co. : Madison. Door Co. : Baileys Harbor as M. affine
var. ciliare (Grev.) C. M. Lincoln Co.: Grandmother Falls.
Marathon Co. : Granite Heights. Oconto Co. : Oconto. Onei¬
da Co.: Noisy Creek; Rainbow Rapids; Whirlpool Rapids.
Outagamie Co. : Medina. Sheboygan Co. : Cedar Grove ; same
station as M . affine var. ciliare (Grev.) C. M. ; Elkhart Lake
as M. affine var. rugicum Bry. Eur. Vilas Co. : Conover.
M. cuspidatum Hedw. Adams Co.: Cold Water Canyon. Ash¬
land Co. : Oak Island. Barron Co. : Barron. Bayfield Co. :
Drummond ; Herbster ; Houghton Quarry ; La Chapelie
(Lashabel’s homestead) ; Port Wing; Sand Bay. Burnett
Co. : Web Lake. Dane Co. : Hook Lake ; Madison. Dodge Co. :
Horicon. Door Co.: Baileys Harbor; Garrett Bay. Douglas
Co. : Amnicon Falls ; Brule River, near Lake Superior. Grant
Co. : Glen Haven ; Potosi. Kewaunee Co. : Kewaunee. Lafay¬
ette Co.: Fayette. Oneida Co.: McNaughton; Noisy Creek;
Rainbow Rapids; Whirpool Rapids. Outagamie Co.: Apple-
Cheney and Evans — The Mosses of Wisconsin 205
ton. Polk Co. : near Doran. Rock Co. : Beloit ; Clinton. Sauk
Co. : Devils Lake. Trempealeau Co. : near Marshland. Vilas
Co. : Conover; Eagle River; Lac Vieux Desert. Washington
Co. : Newburg. Waukesha Co. : Mukwonago ; Ottawa Twp. ;
Pine Lake; Waukesha.
M. Drummondii Bry. Eur. Barron Co. : Barron. Bayfield Co. :
Bark Bay; Drummond; Sand Island; Squaw Bay. Burnett
Co.: Web Lake. Lincoln Co.: Grandmother Falls; Toma¬
hawk. Oneida Co. : Newbold ; Rhinelander ; Tomahawk Lake.
Vilas Co. : Lac Vieux Desert.
M. longirostrum Brid. as M. rostratum Schrad. Dane Co. :
Madison. Jefferson Co. : Palmyra. Oneida Co. : Noisy Creek.
Rock Co.: Bradford Twp.; Clinton. Sheboygan Co.: Cedar
Grove. Waukesha Co. : Mukwonago.
M. lycopomoides (Hook.) Schwaegr. Ashland Co.: Basswood
Island; Stockton Island. Bayfield Co.: Herbster ; Houghton
Quarry ; Port Wing. Douglas Co. : T 45 N R 15 W. Iron Co. :
Montreal River, near Lake Superior. Lincoln Co.: Grand¬
father Falls. Oneida Co. : Noisy Creek.
M. medium Bry. Eur. Ashland Co. : Hermit Island. Barron Co. :
near Barron. Bayfield Co.: Drummond; Port Wing. Bur¬
nett Co. : Web Lake. Douglas Co. : Brule River. Grant Co. :
Glen Haven. Iron Co.: Montreal River, near Lake Superior.
Lincoln Co. : Grandfather Falls ; near Grandfather Falls.
Oneida Co. : Rainbow Rapids ; Whirlpool Rapids. Vilas Co. :
Lac Vieux Desert. Washburn Co. : Spooner.
M. ORTHORHYNCHUM Brid. Ashland Co.: Basswood Island;
Manitou Island. Bayfield Co. : Herbster; Houghton Quarry;
Mason ; Siskowitt Bay. Dodge Co. : Horicon. Door Co. : Elli¬
son Bay ; Sister Bay. Douglas Co. : Manitou Falls ; St. Louis
River. Iron Co. : Montreal River, near Lake Superior. Grant
Co. : Bagley. Lincoln Co. : Grandfather Falls. Oneida Co. :
Noisy Creek ; Whirlpool Rapids.
M. punctatum Hedw. Adams Co.: Cold Water Canyon ;
Witches Gulch. Ashland Co. : Oak Island. Barron Co. : Bar¬
ron. Bayfield Co. : Drummond ; Houghton Quarry ; Port
Wing Dane Co. : Blue Mounds. Door Co. : Baileys Harbor as
M. subglobosum Hpe. Douglas Co. : T 45 N R 15 W. Mara¬
thon Co. : Granite Heights. Oneida Co. : Noisy Creek. Price
Co. : Knox Mills. Sauk Co. : Delton.
206 Wisconsin Academy of Sciences , Arts and Letters
M. PUNCTATUM var. elatum Schimp. Barron Co.: Barron.
Bayfield Co.: Herbster. Burnett Co.: Web Lake. Douglas
Co. : Spruce Creek ; Winneboujou. Iron Co. : La Pointe Indian
Reservation; Montreal River, near Lake Superior. Lincoln
Co. : Tomahawk. Oneida Co. : Noisy Creek ; Tomahawk Lake ;
Whirlpool Rapids. Outagamie Co.: West Center. Ozaukee
Co. : Cedarburg. Price Co. : Knox Mills. Vilas Co. : Lac Vieux
Desert; near State Line Waukesha Co.: Nagawicka Lake.
Wood Co.: Wisconsin Rapids.
M. SEERATUM Brid. Ashland Co. : Oak Island. Bayfield Co. :
Herbster ; Port Wing. Dane Co. : Madison ; Mendota. Doug¬
las Co.: Brule River, near Lake Superior. Grant Co.: Bag-
ley; near Bridgeport; Cornelia; Glen Haven; Mt. Hope;
Potosi. Iron Co. : Montreal River, near Lake Superior. Mil¬
waukee Co. : Wauwatosa. Rock Co. : Beloit.
M. spinulosum Bry. Eur. Adams Co.: Cold Water Canyon.
Ashland Co.: Basswood Island. Bayfield Co.: Bark Bay;
Drummond; La Chapelle (Lashabel’s homestead); Mason;
Sand Bay ; Siskowitt Bay. Door Co. : Baileys Harbor. Doug¬
las Co. : Amnicon River, near Lake Superior ; T 45 N R 15 W.
Iron Co. : Hurley ; Montreal. Lincoln Co. : Grandfather Falls ;
near Grandfather Falls ; Grandmother Falls ; Merrill ; Toma¬
hawk. Marathon Co.: Granite Heights; Mosinee. Oneida
Co.: Hat Rapids; Newbold; Rainbow Rapids; Tomahawk
Lake. Rusk Co. : Ladysmith. Vilas Co. : Conover ; Lac Vieux
Desert; near State Line; Sayner. Washington Co.: New-
burg.
M. stellare Hedw. Barron Co.: Barron. Bayfield Co.: Mason.
Door Co. : Ellison Bay. Oneida Co. : Whirlpool Rapids. Outa¬
gamie Co. : Appleton. Polk Co. : near Doran.
Myurella
M. Careyana Sull. Ashland Co.: Oak Island. Bayfield Co.:
Houghton Quarry. Door Co.: Baileys Harbor. Iron Co.:
Montreal River, near Lake Superior.
M, julacea (Schwaegr.) Bry. Eur. Ashland Co.: Basswood
Island ; Oak Island. Bayfield Co. : Herbster ; Port Wing.
Neckera
N. PENNATA Hedw. Adams Co.: Cold Water Canyon. Ashland
Co. : La Pointe, Madeline Island ; Hermit Island. Barron Co. :
Cheney and Evans — The Mosses of Wisconsin 207
Barron. Bayfield Co. : Drummond ; Houghton Quarry ; Sis-
kowitt Bay. Dane Co. : Madison. Door Co. : Baileys Harbor ;
Ellison Bay. Douglas Co. : T 45 N R 15 W ; Winneboujou.
Iron Co. : N E corner of the La Pointe Indian Reservation ;
Montreal River, near Lake Superior. Lincoln Co.: Grand¬
father Falls; Grandmother Falls. Marathon Co.: Granite
Heights. Oneida Co.: between Eagle River and Tomahawk
Lake; Rhinelander; Tomahawk Lake. Outagamie Co.:
Greenville. Rusk Co.: Weyerhauser. Sheboygan Co.: Cedar
Grove. Vilas Co.: Lac Vieux Desert; near State Line; Star
Lake.
Oncophorus
0. polycarpus (Hedw.) Brid. Ashland Co.: Basswood Island.
Grant Co. : Bagley. Jefferson Co. : Palmyra. Rock Co. : New¬
ark Twp. Trempealeau Co. : Trempealeau.
O. tenellus (Bry. Eur.) Williams. Grant Co.: near Castle
Rock.
0. VIRENS (Hedw.) Brid. Ashland Co.: Basswood Island. Bay-
field Co.: Herbster.
0. VIRENS var. SERRATUS (Bry. Eur.) Limpr. Ashland Co.:
Basswood Island; Oak Island. Bayfield Co. : Port Wing; Sand
Bay; Sand Island; Squaw Bay.
0. Wahlenbergii Brid. Bayfield Co.: Mason. Douglas Co.:
St. Louis River. Iron Co.: Montreal River, near Lake Su¬
perior. Lincoln Co. : Merrill. Marathon Co. : Granite Heights.
Oneida Co.: McNaughton; Rhinelander; Tomahawk Lake;
Whirlpool Rapids. Rock Co. : Beloit. Vilas Co. : Eagle River ;
Lac Vieux Desert.
Orthotrichum
O. anomalum Hedw. Ashland Co.: Basswood Island. Bayfield
Co. : Bayfield. Houghton Quarry. Dane Co. : Madison. Door
Co. : Baileys Harbor ; Ellison Bay. Lincoln Co. : Grandfather
Falls. Outagamie Co. : Appleton. Ozaukee Co. : Grafton.
Rock Co.: Bradford Twp. Waukesha Co.: Pewaukee; Pine
Lake.
O. elegans Hook. & Grev. Ashland Co. : Madeline Island ; Mani-
tou Island; White River; Hermit Island. Barron Co.: Bar¬
ron ; Maple Grove Twp. Bayfield Co. : Herbster ; Mason ; Port
Wing. Burnett Co.: Web Lake. Dane Co.: Madison. Doug-
208 Wisconsin Academy of Sciences , Arts and Letters
las Co. : Amnicon River, near Lake Superior. Iron Co. : N W
corner of La Pointe Indian Reservation; Montreal River,
near Lake Superior. Lincoln Co.: Tomahawk. Oneida Co.:
Newbold; Rhinelander. Rock Co.: Newark Twp. Rusk Co.:
Sand Lake. Vilas Co. : Lac Vieux Desert.
0. Lescurii Aust. Dane Co. : near Madison. Dodge Co. : Hori-
con. Grant Co.: Andersons Mills; Bagley; Beetown; Cass-
ville ; Glen Haven ; Potosi. Rock Co. : Avon Twp. ; Bradford
Twp. ; Newark Twp. Waukesha Co. : Menomonee Falls.
0. OBTUSIFOLIUM Brid. Barron Co. : Barron ; Barron Twp. ;
Maple Grove Twp. ; Stanfold Twp. Bayfield Co. : Port Wing.
Dane Co.: Hook Lake. Grant Co.: Glen Haven; North An¬
dover; Platteville; Potosi. Lincoln Co.: Grandmother Falls;
Tomahawk. Oneida Co. : Hat Rapids. Polk Co. : near Doran.
Rock Co. : Bradford Twp. ; Clinton ; Newark Twp. Vilas Co. :
Lac Vieux Desert.
O. OHIOENSE Sull. & Lesq. Barron Co.: Barron; Maple Grove
Twp. ; Sumner Twp. Rusk Co. : Rusk Twp.
O. PUMILUM Dicks. Barron Co. : Barron. Dane Co. : Madison.
Grant Co. : Bagley ; Dutch Hollow, near Potosi ; Glen Haven ;
Platteville ; Potosi. Jefferson Co. : Palmyra. Rock Co. : near
Allens Grove ; Beloit ; Bradford Twp. ; Clinton ; near Clinton ;
Janesville. Walworth Co. : Whitewater. Waukesha Co. :
Mouse Lake; Oconomowoc; Oconomowoc Lake; Pine Lake;
Waukesha.
0. SORDIDUM Lesq. & James. Barron Co. : Barron ; Doyle Twp.
Bayfield Co.: Bark Bay; Bayfield; Drummond; Herbster;
Mason; Siskowitt Bay. Burnett Co.: Web Lake. Dane Co.:
Middleton. Douglas Co.: Falls of the Black River; Brule
River, near Lake Superior ; Lake Superior, near mouth of the
Amnicon River. Grant Co. : Potosi. Iron Co. : Montreal Riv¬
er, near Lake Superior. Marathon Co. : Wausau. Sheboygan
Co. : Cedar Grove. Vilas Co. : Lac Vieux Desert.
0. 8TELLATUM Brid. Ashland Co.: Madeline Island; Manitou
Island. Barron Co. : Barron ; Barron Twp. Burnett Co. : Web
Lake. Dane Co.: Hook Lake; Madison. Grant Co.: Glen
Haven; Platteville; Potosi; Woodman. Lafayette Co.: Fay¬
ette. Marathon Co. : Mosinee. Oneida Co. : Rhinelander.
Portage Co. : Stevens Point.
Cheney and Evans — The Mosses of Wisconsin 209
Paraleucobryum
P. longifolium (Hedw.) Loeske. Marathon Co.: Granite
Heights. Oneida Co.: near Rhinelander; Hat Rapids; be¬
tween Lake Julia and Newbold. Vilas Co. : Lac Vieux Desert.
Phascum
P. CUSPIDATUM Hedw. Barron Co. : Barron Twp., sec. 28. Dane
Co. : Madison. Grant Co. : Glen Haven ; near Potosi. Wauke¬
sha Co. : near Menomonee Falls ; near Mukwonago ; near
Waukesha.
P. cuspidatum var. americanum Ren. & Card. The stations
marked with an * indicate collections identified as P. cuspida-
tum var. piliferum (Schreb.) Hook. Barron Co.: Barron
Twp., secs. 28 and 85 *. Grant Co.: Bagley; Glen Haven;
Potosi ; same station *.
Philonotis
P. calcarea (Bry. Eur.) Schimp. Dane Co.: Madison.
P. fontana (Hedw.) Brid. Adams Co.: Dells of the Wisconsin
River. Ashland Co.: Basswood Island. Barron Co.: Barron.
Bayfield Co.: Roy's Point, the old landing near Redcliff;
Drummond; Siskowitt Bay. Dane Co.: Windsor. Douglas
Co.: Upper Lucius Lake. Grant Co.: Glen Haven; Potosi.
Lincoln Co.: near Grandfather Falls. Marathon Co.: Mosi-
nee. Oneida Co.: Noisy Creek. Vilas Co.: along Wisconsin
River. Waukesha Co. : near Mukwanago.
Physcomitrium
P. Hookeri Hampe. Buffalo Co. : Marshland.
P. immersum Sull. Barron Co.: Barron. Waukesha Co.: Fos¬
ter's Woods, Fox River.
P. Kellermani E. G. Britton. Rock Co. : Beloit.
P. turbinatum (Mx.) Brid. Barron Co.: Barron. Dane Co.:
Madison. Grant Co.: near Glen Haven; Potosi. Lafayette
Co. : Fayette. Milwaukee Co. : North Milwaukee. Rock Co. :
Bradford Twp., Carver's Rocks. Waukesha Co. : Eagle ; Fos¬
ter's Woods, Fox River; Menomonee Falls; Oconomowoc
Lake; Waukesha.
Plagiobryum
P. demissum (Hoppe & Hornsch.) Lindb. Grant Co.: Potosi;
210 Wisconsin Academy of Sciences , Arts and Letters
near Potosi. Rock Co.: Janesville. Waukesha Co.: Eagle;
Waukesha.
P. Zierii (Hedw.) Lindb. Waukesha Co.: near Waukesha.
Plagiopus
P. Oederi (Brid.) Limpr. as Bartramia Oederi Schwaegr. Cal¬
umet Co. : Highcliff. Columbia Co. : Wisconsin Dells. Craw¬
ford Co.: near Bridgeport. Door Co.: Baileys Harbor; Elli¬
son Bay. Douglas Co.: Falls of the Black River; Manitou
Falls. Grant Co.: Andersons Mills; Bagley; near Bridge¬
port ; Glen Haven ; Mt. Hope ; North Andover ; Potosi. Lafay¬
ette Co. : Fayette. Outagamie Co. : Appleton. Sauk Co. : Dev¬
ils Lake.
Plagiothecium
P. DENTICULATUM (Hedw.) Bry. Eur. Ashland Co.: Hermit Is¬
land. Barron Co.: Barron. Bayfield Co.: Drummond; Herb-
ster ; Houghton Quarry ; Mason ; Sand Island. Dane Co. : Mc¬
Farland. Douglas Co. : mouth of Brule River. Jefferson Co. :
Lake Mills; Palmyra; Sullivan. Lincoln Co.: Grandfather
Falls ; between Merrill and Grandfather Falls ; between
Grandmother Falls and Gilbert; between Grandmother Falls
and Tomahawk; near Rainbow Rapids. Milwaukee Co.:
South Milwaukee. Oneida Co.: Noisy Creek; Rhinelander.
Outagamie Co.: Medina Swamp. Ozaukee Co.: Cedarburg
Swamp. Rock Co.: Clinton; near Fairfield. Sheboygan Co.:
Cedar Grove. Vilas Co. : Lac Vieux Desert. Washington Co. :
Barth's Swamp. Waukesha Co. : near Calhoun ; Eagle Lake ;
Mukwonago ; Vernon Station ; near Waukesha. Wood Co. :
Wisconsin Rapids.
P. DENTICULATUM f . propaguliferu M Ruthe. Barron Co. : Bar¬
ron Twp., secs. 5, 20, 32. Jefferson Co. : near Helenville; Pal¬
myra ; Sullivan. Waukesha Co. : Waukesha.
P. deplanatum (Sull.) Grout. Jefferson Co. : Sullivan. Wauke¬
sha Co.: Waukesha.
P. geophilum (Aust.) Grout. Grant Co.: Glen Haven; Lan¬
caster; Potosi.
P. laetum Bry. Eur. Grant Co.: Potosi. Oneida Co.: Noisy
Creek.
P. latebricola (Wils.) Bry. Eur. Barron Co.: Clinton Twp.:
Four Mile Swamp.
Cheney and Evans — The Mosses of Wisconsin 211
P. MICANS (Sw.) Paris. Washington Co.: Newburg.
P. pulchellum (Hedw.) Bry. Eur. Bayfield Co.: Drummond;
La Chapelle (Lashabel’s homestead) ; Sand Bay. Douglas
Co. : T 45 N R 15 W as P. passaicense Aust. ( ?) . Iron Co. :
Montreal River. Lincoln Co.: Whirpool Rapids. Outagamie
Co. : Medina Swamp. Vilas Co. : along the Wisconsin River.
P. Roeseanum (Hampe) Bry. Eur. Barron Co.: Four Mile
Swamp. Grant Co. : Bagley ; Mt. Hope ; Patch Grove.
P. Ruthei Limpr. Barron Co. : near Barron.
P. Seligerx (Brid.) Lindb. Outagamie Co.: Greenville.
P. STEIATELLUM (Brid.) Lindb. Bayfield Co. : Herbster. Colum¬
bia Co. : Wisconsin Dells. Oneida Co. : Newbold.
P. sylvaticum (Brid.) Bry. Eur. Adams Co.: Cold Water Can¬
yon. Barron Co.: Barron. Dane Co.: Blue Mounds; Windsor.
Sheboygan Co. : Oostburg. Waukesha Co. : Pine Lake.
P. turfaceum (Lindb.) Lindb. Ashland Co.: Basswood Island;
Manitou Island. Bayfield Co. : Drummond ; Roy's Point, the
old landing near Redcliff ; Sand Island ; Siskowitt Bay. Door
Co. : Baileys Harbor. Douglas Co. : West Superior. Iron Co. :
near Montreal. Lincoln Co. : Grandfather Falls ; Grandmoth¬
er Falls; between Grandmother Falls and Gilbert; Merrill;
between Merrill and Grandfather Falls; near Tomahawk.
Manitowoc Co. : Two Rivers. Marathon Co. : Granite Heights.
Oneida Co.: Dorothy Lake; Newbold; Rhinelander. Outa¬
gamie Co.: Greenville; Medina Swamp; West Center Swamp.
Sheboygan Co.: Cedar Grove; Little Elkhart Lake. Vilas
Co.: between Conover and Eagle River; below Eagle River,
near rapids in Wisconsin River; Lac Vieux Desert; Sayner.
Waukesha Co. : Lower Nashotah Lake.
Platygyrium
P. repens (Brid.) Bry. Eur. Adams Co.: Cold Water Canyon;
Dells of the Wisconsin River. Ashland Co.: Hermit Island.
Barron Co. : Canton ; Four Mile Creek. Bayfield Co. : Drum¬
mond ; Herbster ; Houghton Quarry ; Orienta. Dane Co. : Blue
Mounds; Middleton. Douglas Co.: Upper Lucius Lake; sec.
10 T 46 N R 10 W. Grant Co.: Bloomington; Glen Haven;
Patch Grove. Jefferson Co.: Helenville; Palmyra. Lafayette
Co.: Fayette. Lincoln Co.: Grandmother Falls; between
Grandmother Falls and Gilbert. Milwaukee Co.: Donges
Bay; West Allis. Outagamie Co.: near Readfield. Ozaukee
212 Wisconsin Academy of Sciences, Arts and Letters
Co. : Cedarburg. Rusk Co. : sec. 20 T 36 N R 7 W. Sheboygan
Co.: Cedar Grove. Vilas Co.: Lac Vieux Desert. Waukesha
Co.: Bark River; Foster's Woods, Fox River; Mukwonago
Marsh; Nemahbin Lake; Pine Lake; Saylesville; Waukesha.
Pleuridium
P. subulatum (Hedw.) Lindb. The stations marked with an *
indicate collections identified as P. a Iternifolium (Dicks.,
Kaulf.) Rabenh. Barron Co.: Barron *; Barron Twp.; same
station *. Dane Co.: Madison. Grant Co.: Bagley; Glen
Haven; same station *; Potosi; same station *. Rock Co.:
Beloit. Waukesha Co.: Delafield Twp. ; Lower Nashotah
Lake; Menomonee Falls; Mukwonago; same station *; New
Berlin *; Oconomowoc; Prospect; Summit Twp.; Waukesha
* ; Waukesha Twp.
POGONATUM
P. alpinum (Hedw.) Rohl. Adams Co.: Dells of the Wisconsin
River. Ashland Co.: Basswood Island; Oak Island. Bayfield
Co. : Herbster ; Houghton ; Houghton Quarry ; between Port
Wing and Orienta ; Sand Bay ; between Sand Bay and Squaw
Bay; Sand Island. Juneau Co.: near Quincy. Lincoln Co.:
one mile above Pine River. Marathon Co. : Granite Heights ;
between Mosinee and Wausau.
P. ALPINUM var. SEPTENTRIONALE (Rohl.) Brid. Bayfield Co.:
between Herbster and Port Wing.
P. urnigerum (Hedw.) Beauv. Chippewa Co.: Chippewa Falls.
POHLIA
P. acuminata Hoppe & Hornsch. Adams Co. : Cold Water Can¬
yon; Dells of the Wisconsin River; Witches Gulch. Barron
Co.: Maple Grove Twp.; Prairie Lake Twp. Bayfield Co.:
between Herbster and Port Wing; Sand Bay. Dane Co. : Blue
Mounds. Grant Co. : Patch Grove. Iron Co. : Montreal River.
Lafayette Co. : Argyle ; Fayette.
P. annotina (Hedw.) Loeske. Barron Co.: Prairie Lake Twp.
P. cruda (Hedw.) Lindb. Bayfield Co.: Mason. Grant Co.: Glen
Haven ; Patch Grove. Iron Co. : Montreal River. Lincoln Co. :
Grandfather Falls; near Grandfather Falls; between Grand¬
father Falls and Merrill; above Pine River. Marathon Co.:
between Wausau and Mosinee.
Cheney and Evans— The Mosses of Wisconsin
213
P. cucullata (Schwaegr.) Bruch. Grant Co.: Werley. Mara¬
thon Co.: between Mosinee and Wausau. Oneida Co.: be¬
tween Lake Julia and Newbold ; Whirlpool Rapids. Vilas Co. :
Lac Vieux Desert. Waukesha Co. : Menomonee Twp.
P. delicatula (Hedw.) Grout, as Web era carnea Schimp.
Marathon Co. : Goodrich Junction.
P. elongata Hedw. Adams Co. : Dells of the Wisconsin River.
Ashland Co.: Basswood Island; Oak Island. Barron Co.:
Four Mile Creek. Bayfield Co. : Houghton Quarry. Lafayette
Co. : Fayette.
P. filiform is (Dicks.) Andrews as Anomobryum concinnatum
(Spruce) Lindb. These collections, some of which are fertile,
seem to compare favorably with Anomobryum fili forme
(Dicks.) Husn. Die Laubmoose Europas IV Band: 416, 417.
Ashland Co.: Basswood Island. Barron Co.: Maple Grove
Twp. Bayfield Co. : Herbster ; Houghton Quarry. Grant Co. :
Bagley.
P. NUTANS (Hedw.) Lindb. Ashland Co.: Basswood Island;
Manitou Island; Oak Island. Barron Co.: near Cameron.
Bayfield Co.: Drummond; Houghton Quarry; Orienta; be¬
tween Sand Bay and Squaw Bay; Siskowitt Bay. Columbia
Co.: Wisconsin Dells. Dane Co.: Hook Lake. Door Co.:
Baileys Harbor. Douglas Co.: Brule River; Lucius Lake;
St. Louis River. Grant Co. : Bagley ; near Glen Haven. Jun¬
eau Co. : Germantown. Lincoln Co. : Grandfather Falls ;
Grandmother Falls; Tomahawk; near Pine River; between
Tomahawk and Nigger Island. Marathon Co. : Granite
Heights. Oneida Co.: Dorothy Lake; Newbold; between
Newbold and McNaughton; between Lake Julia and New-
bold; near Tomahawk Lake; Whirlpool Rapids. Outagamie
Co.: Binghampton Bog. Sheboygan Co.: Crystal Lake; Ply¬
mouth ; Terry Andrae Park. Vilas Co. : Conover ; Lac Vieux
Desert; Military Road, near Forest Co. line; between Plum
and Razor Back Lakes; along the Wisconsin River. Wauke¬
sha Co.: near Calhoun; Menomonee Falls; Pine Lake; Sus¬
sex ; Wales.
P. proligera Lindb. Barron Co.: Maple Grove Twp.; Prairie
Lake Twp. Buffalo Co.: Bohri. Dane Co.: Lake Mendota.
Grant Co.: Patch Grove. Iron Co.: Montreal River, near
Lake Superior. Vilas Co. : near Eagle River.
214 Wisconsin Academy of Sciences , Arts and Letters
P. pulchella (Hedw.) Lindb. Grant Co.: Potosi; same station
as P. Lescuriana Sull.
P. Wahlenbergii (Web. & Mohr) Andrews. Dane Co.: Madi¬
son. Grant Co.: Bagley; Dickeysville ; Platteville; Potosi.
Milwaukee Co. : Milwaukee. Oconto Co. : Oconto. Rock Co. :
Clinton; Janesville. Waukesha Co.: Vernon Station. As
Webera albicans Schimp. Ashland Co. : Oak Island. Bayfield
Co.: Houghton Quarry; Mason; between Port Wing and
Herbster ; between Port Wing and Orienta. Lincoln Co. :
Grandfather Falls; Noisy Creek. As P. albicans Lindb.
Grant Co. : Potosi. Sauk Co. : Ironton. Trempealeau Co. :
Crow Branch.
POLYTRICHUM
P. commune Hedw. Adams Co. : Dells of the Wisconsin River.
Ashland Co. : Basswood Island. Bayfield Co. : Drummond.
Buffalo Co.: Marshland. Dane Co.: McFarland; Madison;
Mazomanie. Douglas Co.: Amnicon Lake. Grant Co.: Glen
Haven; Potosi. Iron Co.: Montreal. Juneau Co.: Necedah.
Marathon Co.: Granite Heights. Ozaukee Co.: Cedarburg.
Rock Co.: Bradford Twp., near Carver’s Rocks; Newark
Twp. Vilas Co.: between Conover and Eagle River; Lac
Vieux Desert. Waukesha Co.: Eagle Twp.; Mukwonago;
Wales.
P. formosum Hedw. Lincoln Co. : Tomahawk.
P. gracile Smith. Dane Co.: Madison. Douglas Co.: Brule
River. Lincoln Co. : Tomahawk. Oneida Co. : between Lake
Julia and Newbold. Rock Co.: Newark Twp. Waukesha Co.:
Menomonee Twp.; Pine Lake; Waukesha.
P. juniperinum Hedw. Bayfield Co. : Drummond ; Sand Island.
Burnett Co.: near Swiss, St. Croix River. Columbia Co.:
Wisconsin Dells. Dane Co.: Blue Mounds; Madison. Door
Co. : Baileys Harbor. Douglas Co. : Amnicon Lake. Grant
Co.: Glen Haven. Iron Co.: Montreal. Jefferson Co.: Lake
Mills ; Palmyra. Lafayette Co. : Fayette. Marathon Co. :
Granite Heights. Oconto Co.: Oconto. Oneida Co.: Three
Lakes. Ozaukee Co. : Port Washington. Rock Co. : Hanover.
Sauk Co. : Delton. Sheboygan Co. : Crystal Lake ; Sheboygan.
Vilas Co. : Lac Vieux Desert ; near Lac Vieux Desert. Wash¬
burn Co. : Spooner. Waukesha Co. : Eagle Lake ; Oconomo-
woc ; Waukesha.
Cheney and Evans — The Mosses of Wisconsin 215
P. juninerinum var. alpestre Bry. Eur. Dane Co. : Madison.
Douglas Co.: Solon Springs. Rock Co.: Fairfield. Sawyer
Co. : Seeley. Vilas Co. : Conover. Washington Co. : Newburg.
P. OHIOENSE Ren. & Card. Barron Co.: Barron; Four Mile
Creek. Bayfield Co. : Sand Island. Dane Co. : Madison. Doug¬
las Co. : Brule River. Grant Co. : Potosi. Jefferson Co. : Pal¬
myra. Lincoln Co.: Gilbert; Grandfather Falls; between
Grandfather Falls and Merrill. Marathon Co. : Granite
Heights. Milwaukee Co. : Milwaukee. Oneida Co. : near
Rhinelander; Tomahawk Lake. Rock Co.: Newark Twp.
Vilas Co.: Conover; between Conover and Eagle River; Lac
Vieux Desert ; Sayner. Waukesha Co. : Pine Lake.
P. piliferum Hedw. Adams Co. : Dells of the Wisconsin River.
Ashland Co.: Kakagin River. Barron Co.: Yellow River,
Stanfold Twp. Bayfield Co.: Houghton Quarry. Dane Co.:
Pine Bluff. Grant Co. : Millville. Iron Co. : Montreal. Jeffer¬
son Co.: Palmyra. Juneau Co.: Point Bluff, near Mauston.
Marathon Co. : Mosinee. Oneida Co. : Newbold ; Stump Land¬
ing, near Newbold. Rock Co. : Newark Twp. Sheboygan Co. :
Cedar Grove. Vilas Co. : Conover.
Pylaisia
P. intricata (Hedw.) Bry. Eur. Adams Co.: Dells of the Wis¬
consin River. Dane Co. : Madison. Iron Co. : Montreal. Jef¬
ferson Co. : Helenville. Lafayette Co. : Fayette. Lincoln Co. :
Grandmother Falls; Rainbow Rapids. Oneida Co.: Mc-
Naughton; Tomahawk Lake; Wisconsin River. Vilas Co.:
between Tomahawk Lake and Eagle River ; Star Lake. Wau¬
kesha Co. : Oconomowoc Lake.
P. polyantha Bry. Eur. Ashland Co.: Oak Island. Barron
Co. : Barron Twp., sec. 8. Bayfield Co. : Buffalo Bay ; Mason.
Brown Co. : Green Bay. Douglas Co. : Brule River ; St. Louis
River. Jefferson Co.: near Sullivan. Lincoln Co.: Grand¬
mother Falls; between Grandmother Falls and Gilbert; be¬
tween Grandmother Falls and Tomahawk ; Tomahawk. Onei¬
da Co. : Dorothy Lake ; Hat Rapids ; along Wisconsin River.
Rock Co.: Bradford Twp.; Clinton. Vilas Co.: Lac Vieux
Desert; Pine Lake; along Wisconsin River.
P. Selwynii Kindb. Ashland Co. : Hermit Island. Barron Co. :
Barron. Bayfield Co.: Herbster; Houghton Quarry; Mason;
Port Wing. Dane Co.: Madison as P. S chimp eri Cardot.
216 Wisconsin Academy of Sciences , Arts and Letters
Douglas Co. : St. Louis River. Grant Co. : Glen Haven ; Platte-
ville. Lincoln Co.: between Gilbert and Grandmother Falls;
Grandmother Falls; Rainbow Rapids as P. Schimperi Car-
dot ; Whirlpool Rapids. Oneida Co. : Newbold ; Rhinelander ;
Tomahawk Lake ; along Wisconsin River. Rock Co. : Clinton.
Vilas Co.: Lac Vieux Desert; same station as P. Schimperi
Cardot; near Lac Vieux Desert; near Eagle River. Wauke¬
sha Co. : Hartland ; North Lake ; Pine Lake ; Waukesha.
P. subdenticulata Schimp. Barron Co.: Barron Twp. Bay-
field Co. : Mason ; Orienta. Douglas Co. : Brule River. Oneida
Co. : Rhinelander ; along Wisconsin River.
Rhabdoweisia
R. denticulata (Brid.) Bry. Eur. Adams Co.: Dells of the
Wisconsin River. Bayfield Co.: Houghton Quarry.
R. DENTICULATA var. Americana Culmann. as R. fug ax (Hedw.)
Bry. Eur. Adams Co. : Dells of the Wisconsin River.
Rhodobryum
R. roseum (Bry. Eur.) Limpr. Ashland Co.: Penokee Iron
Range. Bayfield Co.: Herbster. Dane Co.: Blue Mounds;
Madison. Douglas Co. : T 44 N R 15 W ; Upper Lucius Lake.
Iron Co. : Montreal ; Montreal River. Lafayette Co. : Fayette.
Oconto Co.: Oconto. Price Co.: Ogema. Rusk Co.: Bruce.
Sheboygan Co.: Cedar Grove; Evergreen Park. Washington
Co.: Newburg. Waukesha Co.: Foster’s Woods, Fox River.
Rhytidiadelphus
R. triquetrus (Hedw.) Warnst. Dane Co.: Pine Bluff. Doug¬
las Co.: Brule River. Grant Co.: Glen Haven; Montfort;
Mt. Hope; Platteville. Iron Co.: near Montreal. Jefferson
Co. : Palmyra. Lafayette Co. : Fayette. Lincoln Co. : Grand¬
mother Falls ; Whirlpool Rapids. Milwaukee Co. : South Mil¬
waukee. Oneida Co. : Tomahawk Lake. Outagamie Co. : West
Center Swamp. Ozaukee Co. : Cedarburg. Rock Co. : Brad¬
ford Twp. Rusk Co. : sec. 20 T 36 N R 7 W ; near Bruce.
Sheboygan Co.: Cedar Grove; Sheboygan. Waukesha Co.:
Beaver Lake.
Rhytidium
R. RUGOSUM (Hedw.) Kindb. Ashland Co.: Loon Lake, near
Cheney and Evans — The Mosses of Wisconsin
217
Mellen ; Mellen. Bayfield Co. : Fort Wing. Dane Co. : Black
Earth. Grant Co.: Glen Haven. Iron Co.: Montreal River.
Saelania
S. GLAUCESCENS (Hedw.) Broth. Bayfield Co.: Sand Island.
Dane Co. : Blue Mounds. Douglas Co. : St. Louis River. Grant
Co. : Bagley ; Montfort. Lafayette Co. : Fayette. Lincoln Co. :
between Grandfather Falls and Merrill. Marathon Co. : near
Pine River. Sauk Co. : Pine Hollow, Baraboo Hills.
SCHWETSCHKEOPSIS
S. DENTICULATA (Sull.) Broth. Grant Co. : Potosi.
SCORPIDIUM
S. SCORPIOIDES (Hedw.) Limpr. Bayfield Co. : Port Wing, Outa¬
gamie Co.: Medina Swamp.
Seligeria
S. pusilla (Hedw.) Bry. Eur. Grant Co.: Bagley; Beetown;
Burton ; Glen Haven ; North Andover ; Wyalusing.
S. recurvata (Hedw.) Bry. Eur. Grant Co.: Glen Haven.
Sematophyllum
S. carolinianum (C. Mull.) E. G. Britton, as Rayhidostegium
carolinianum (C. Mull.) Jaeger & Sauerb. Grant Co.: Castle
Rock.
Splachnum
S. ampullaceum Hedw. Barron Co. : near Cameron.
Sphagnum
S. capillaceum (Weiss) Schrank. Ashland Co.: Basswood Is¬
land; Madeline Island; Penokee Iron Range; Hermit Island.
Barron Co.: Barron Twp. Bayfield Co.: Bark Bay. Dane
Co.: Madison. Door Co.: Baileys Harbor. Douglas Co.: op¬
posite Old Fond du Lac, Minn. Jefferson Co.: Palmyra.
Oneida Co.: McNaughton ; Newbold; Pelican Lake; Rhine¬
lander. Outagamie Co.: Binghamton Bog, near Appleton.
Ozaukee Co.: Cedarburg. Rock Co.: Newark Twp. Vilas
Co. : Eagle River ; Lac Vieux Desert. Washington Co. : New-
burg. Waukkesha Co. : Wales.
218 Wisconsin Academy of Sciences , Arts and Letters
S. CAPILLACEUM var. TENELLUM (Schimp.) Andrews. Barron
Co.: Barron Twp. Chippewa Co.: Long Lake.
S. centrals C. Jens. Barron Co. : Barron Twp., secs. 20 and 32.
Waukesha Co.: Menomonee Twp.
S. COMPACTUM DC. Oneida Co. : McNaughton.
S. CUSPIDATUM Ehrh. Dane Co. : Madison. Outagamie Co. : near
Appleton.
S. Dusenii C. Jens. Oneida Co. : McNaughton. Vilas Co. : State
Line.
S. fimbriatum Wils. Barron Co. : Barron ; Barron Twp. Lafay¬
ette Co. : Fayette. Rusk Co. : Ten Mile Creek, Rusk Twp.
S. fuscum (Schimp.) H. Klinggr. Barron Co.: Barron. Bay-
field Co.: Drummond; Port Wing. Burnett Co.: Web Lake.
Chippewa Co. : Long Lake. Oneida Co. : McNaughton ; New-
bold. Outagamie Co.: Binghampton Bog, near Appleton.
Ozaukee Co. : Cedarburg. Vilas Co. : near State Line. Wau¬
kesha Co. : Wales.
S. Girghensohnii Russow. Ashland Co.: Basswood Island;
Mellen. Barron Co. : Stanley Twp. Bayfield Co. : Bark Bay ;
Drummond ; Herbster ; Houghton Quarry ; La Chapelle
(Lashabel’s homestead); Port Wing. Chippewa Co.: Long
Lake. Dane Co. : Madison, Lake Mendota ; London. Douglas
Co. : near the Amnicon River ; opposite Old Fond du Lac,
Minn. Lincoln Co.: Grandfather Falls; Grandmother Falls;
Merrill ; Pine River ; Tomahawk. Oneida Co. : Rainbow Rap¬
ids; Tomahawk Lake. Vilas Co.: Lac Vieux Desert.
S. IMBRICATUM var. AFFINE (Ren. & Card.) Warnst. Juneau
Co. : Witches Gulch.
S. MAGELLANICUM Brid. Ashland Co. : Basswood Island ; Made¬
line Island ; Mellen. Barron Co. : Barron. Bayfield Co. :
Drummond ; Port Wing. Burnett Co. : Web Lake. Dane Co. :
Madison ; London. Douglas Co. : Solon Springs. Jefferson
Co.: Lake Mills. Lincoln Co.: Grandmother Falls; Merrill;
Tomahawk. Marathon Co.: Granite Heights. Oneida Co.:
McNaughton; Newbold; Rhinelander; Whirlpool Rapids;
Wisconsin River, near Tomahawk Lake. Outagamie Co.:
Binghampton Bog, near Appleton. Ozaukee Co. : Cedarburg.
Portage Co. : near Stevens Point as S. intermedium Russow.
Rock Co. : Newark Twp. Vilas Co. : Eagle River ; near State
Line. Washington Co. : Newburg. Waukesha Co. : Wales.
Cheney and Evans— The Mosses of Wisconsin 219
S. palustre L. Ashland Co. : Penokee Iron Range. Barron Co. :
Barron. Douglas Co.: Brule Swamp; Upper Lucius Lake.
Eau Claire Co. : Eau Claire. Jefferson Co. : Lake Mills. Jun¬
eau Co.: Hustler. Ozaukee Co.: Cedarburg. Portage Co.:
Stevens Point. Washington Co.: Newburg. Waukesha Co.:
Summit Twp. ; Wales.
S. papillosum Lindb. Barron Co.: Barron. Dane Co.: Madi¬
son; London. Vilas Co.: State Line.
S. PLUMULOSUM Roll. Ozaukee Co. : Cedarburg.
S. pulchrum (Lindb.) Warnst. Outagamie Co.: Binghampton
Bog, near Appleton.
S. RECURVUM Beauv. Ashland Co.: Madeline Island. Barron
Co. : Barron Twp. Bayfield Co. : Bark Bay ; Drummond ; Port
Wing; Sand Bay. Burnett Co.: Web Lake. Douglas Co.:
Amnicon River. Oneida Co.: New bold ; Tomahawk Lake.
Ozaukee Co. : Cedarburg. Waukesha Co. : Lake Nagawicka.
S. RECURVUM var. tenue H. Klinggr. Barron Co. : Barron Twp.
Bayfield Co. : Port Wing. Dane Co. : London ; Madison. Jef¬
ferson Co.: Lake Mills. Lincoln Co.: Merrill; Tomahawk.
Oneida Co. : McNaughton ; Newbold ; Rainbow Rapids ;
Tomahawk Lake. Ozaukee Co.: Cedarburg. Sauk Co.: Del-
ton. Vilas Co.: Eagle River; Lac Vieux Desert; State Line.
S. RIPARIUM Angstr. Bayfield Co.: Drummond.
S. ROBUSTUM (Russow) Roll. Iron Co.: La Pointe Indian Reser¬
vation. Lincoln Co.: Tomahawk. Outagamie Co.: Appleton.
S. SQUARROSUM Crome. Ashland Co.: Basswood Island; Made¬
line Island; Penokee Iron Range; Hermit Island. Barron
Co.: Barron. Bayfield Co.: Bark Bay; Drummond; Orienta;
Port Wing. Lincoln Co.: Grandfather Falls; Grandmother
Falls; Merrill; Pine River. Oneida Co.: Tomahawk Lake.
Rock Co.: Newark Twp. Rusk Co.: Sand Lake, Big Bend
Twp. ; Wilkinson Twp., sec. 22. Vilas Co. : State Line. Wau¬
kesha Co.: Menomonee Twp.; Waukesha.
S. subsecundum Nees. Barron Co. : Barron Twp. ; Maple Grove
Twp. Bayfield Co. : Drummond ; Port Wing as S. contortum
(Schultz) Limpr. Dane Co.: Madison. Juneau Co.: Dells of
the Wisconsin River. Lincoln Co.: Pine River; Tomahawk.
Oneida Co.: McNaughton; Clear Lake as S. rufescens
Limpr.; Newbold; Tomahawk Lake; same station as S. obe-
sum Wils. Outagamie Co. : Binghampton Bog, near Appleton.
220 Wisconsin Academy of Sciences, Arts and. Letters
Portage Co.: Stevens Point as S. inundatum Russow. Sauk
Co.: Delton. Vilas Co.: Lac Vieux Desert; same station as
S. rufescens Limpr.
S. TENELLUM Pers. Waukesha Co.: Wales.
S. teres (Schimp.) Angstr. Adams Co.: Witches Gulch. Bar¬
ron Co.: Barron Twp. Bayfield Co.: Port Wing. Door Co.:
Baileys Harbor. La Crosse Co. : West Salem. Vilas Co. : Lac
Vieux Desert. Waukesha Co. : Oconomowoc ; Waukesha.
S. Warnstorfii Russow. Ashland Co.: La Pointe, Madeline
Island. Barron Co. : Barron Twp. Bayfield Co. : Port Wing.
Burnett Co. : Web Lake. Door Co. : Baileys Harbor. Douglas
Co.: opposite Old Fond du Lac, Minn.; Upper Lucius Lake.
Iron Co. : La Pointe Indian Reservation. Jefferson Co. : Pal¬
myra. Lincoln Co. : Whirlpool Rapids. Outagamie Co. : Ap¬
pleton. Ozaukee Co.: Cedarburg. Vilas Co.: Lac Vieux Des¬
ert. Waukesha Co. : Waukesha.
S. Wulfianum Girg. Ashland Co. : Penokee Iron Range. Bar¬
ron Co. : Barron. Burnett Co. : Web Lake. Door Co. : Baileys
Harbor. Douglas Co.: mouth of Amnicon River; mouth of
Brule River. Lincoln Co. : Grandmother Falls ; Merrill. Onei¬
da Co.: Newbold; Rainbow Rapids; Tomahawk Lake. She¬
boygan Co.: Crystal Lake. Vilas Co.: Eagle River; State
Line. Washington Co. : Newburg.
Tetraphis
T. pellucid A Hedw. Ashland Co. : La Pointe, Madeline Island ;
Oak Island. Barron Co. : near Barron. Bayfield Co. : Herb-
ster; Mason; Port Wing; Squaw Bay; Siskowitt Bay. Dane
Co. : Windsor. Door Co. : Baileys Harbor. Douglas Co. : Brule
Swamp. Grant Co. : Mt. Hope ; Patch Grove. Iron Co. : Mon¬
treal River. Jefferson Co.: Lake Mills; Sullivan. Lafayette
Co. : Fayette. Lincoln Co. : between Grandfather Falls and
Merrill ; Grandmother Falls. Marathon Co. : Granite Heights ;
between Mosinee and Wausau. Oneida Co. : Newbold. Outa¬
gamie Co.: West Center Swamp. Ozaukee Co.: Cedarburg
Swamp. Sheboygan Co. : Cedar Grove. Vilas Co. : along the
Wisconsin River. Washington Co. : Newburg. Waukesha
Co.: near Menomonee Falls; Vernon Station. Wood Co.:
Wisconsin Rapids.
Cheney and Evans — The Mosses of Wisconsin 221
Thelia
T. asprella Sull. Dane Co. : Blue Mounds ; Madison. Grant Co. :
Glen Haven; Lancaster; Potosi. Jefferson Co.: Lake Mills;
Milford ; Palmyra. Lafayette Co. : Fayette. Rock Co. : Brad¬
ford Twp. ; Newark Twp. Sauk Co.: Baraboo. Waukesha
Co.: Beaver Lake; Mukwonago Marsh; Nashotah; Lower
Nashotah Lake; Upper Nemahbin Lake; Okauchee Lake;
near Pine Lake; Saylesville; Waukesha.
T. hirtella (Hedw.) Sull. Barron Co.: Four Mile Swamp.
Dane Co. : Lake Wingra. Dodge Co. : Horicon.
T. Lescurii Sull. Adams Co.: Dells of the Wisconsin River.
Dane Co.: Mazomanie; Pine Bluff. Grant Co.: near Wood¬
man. Jefferson Co.: Palmyra. Rock Co.: Newark Twp.
Thuidium
T. abietinum (Brid.) Bry. Eur. Ashland Co.: Mellen. Bay-
field Co.: Mason; Orienta; Port Wing; between Port Wing
and Herbster. Dodge Co.: Horicon. Door Co.: Ellison Bay.
Grant Co. : Glen Haven. Iron Co. : Montreal River. Lincoln
Co.: between Grandfather Falls and Merrill as T. scitum.
Outagamie Co. : near Readfield. Waukesha Co. : Eagle Lake
as T. scitum.
T. delicatulum (Hedw.) Mitt. Adams Co.: Dells of the Wis¬
consin River. Ashland Co. : Hermit Island. Bayfield Co. :
Drummond. Dane Co.: Blue Mounds; Lake Wingra; Men-
dota; Windsor. Douglas Co.: Upper Lucius Lake. Grant
Co. : Burton ; Glen Haven ; Platteville. Oneida Co. : Hat Rap¬
ids; Rhinelander; Tomahawk Lake. Outagamie Co.: West
Center Swamp. Price Co. : sec. 35 T 35 N R 2 E. Rock Co. :
Clinton. Rusk Co. : sec. 20 T 36 N R 7 W. Sheboygan Co. :
Cedar Grove. Waukesha Co. : Mukwonago Marsh.
T. microphyllum (Hedw.) Best. Barron Co.: sec. 20 T 34 N R
12 W. Bayfield Co.: Drummond. Grant Co.: Glen Haven.
Marathon Co.: Granite Heights. Oneida Co.: Noisy Creek;
Rhinelander. Portage Co.: near Knowlton. Vilas Co.: Lac
Vieux Desert.
T. minutulum (Hedw.) Bry. Eur. Barron Co.: Four Mile
Swamp. Bayfield Co.: near Mason. Dane Co.: Madison.
Grant Co. : Glen Haven. Lafayette Co. : Fayette. Vilas Co. :
along Wisconsin River as T. scitum.
222 Wisconsin Academy of Sciences, Arts and Letters
T. Philiberti Limpr. Bayfield Co.: Herbster. Door Co.: Bai¬
leys Harbor. Grant Co.: Glen Haven. Lincoln Co.: Grand¬
mother Falls ; Whirlpool Rapids. Oneida Co. : near Newbold ;
along Wisconsin River. Vilas Co.: Lac Vieux Desert. Wash¬
ington Co. : Newburg.
T. pygmaeum Bry. Eur. Grant Co.: Glen Haven; Potosi.
T. RECOGNITUM (Hedw.) Lindb. Adams Co.: Cold Water Can¬
yon; Artists Glen, Dells of the Wisconsin River. Door Co.:
Baileys Harbor. Douglas Co. : St. Louis River. Grant Co. :
Mt. Hope; Platteville. Iron Co.: Montreal. Lincoln Co.:
Grandmother Falls. Milwaukee Co. : South Milwaukee.
Ozaukee Co. : Cedarburg Swamp. Rock Co. : Clinton. Sauk
Co.: Devils Lake. Sheboygan Co.: Cedar Grove. Vilas Co.:
Lac Vieux Desert. Washington Co. : Newburg. Waukesha
Co.: North Lake; Mukwonago Marsh; Pine Lake. Wood
Co. : Wisconsin Rapids.
T. scitum (Beauv.) Aust. Ashland Co.: Glidden. Bayfield Co.:
Drummond ; Mason. Dane Co. : Madison. Lincoln Co. :
Grandmother Falls. Vilas Co. : Lac Vieux Desert.
T. scitum var. aestivale Aust. Barron Co. : Four Mile Swamp
as T. scitum . Dane Co.: Madison. Rusk Co.: Sec. 20 T 36
N R 7 W as T. scitum.
T. VIRGINIANUM (Brid.) Lindb. Barron Co.: Four Mile Swamp.
Bayfield Co.: Mason. Dane Co.: Pine Bluff as T. scitum .
Grant Co.: Bagley; Glen Haven. Jefferson Co.: Palmyra.
Lincoln Co. : Tomahawk. Oneida Co. : McNaughton. Rock
Co.: Newark Twp. Vilas Co.: between Eagle River and
Tomahawk Lake. Waukesha Co. : Martin's Woods, Big Bend ;
Waukesha.
Timmia
T. megapolitana Hedw. Barron Co. : sec. 20 T 34 N R 12 W.
Bayfield Co.: Mason. Douglas Co.: St. Louis River. Grant
Co.: Montfort. Outagamie Co.: Mosquito Hill.
T. MEGAPOLITANA f. CUCULLATA (Rich.) Sayre. Dane Co.: Madi¬
son as T. cucullata Mx. Dodge Co. : Horicon. Grant Co. :
Potosi. Waukesha Co.: Waukesha.
Tortella
T. CAESPITOSA (Schwaegr.) Limpr. Grant Co.: Glen Haven.
Jefferson Co.: Lake Mills; Palmyra. Milwaukee Co.: South
Cheney and Evans — The Mosses of Wisconsin
223
Milwaukee. Ozaukee Co. : Cedarburg. Waukesha Co. : Upper
Nemahbin Lake; Pine Lake.
T. fragxlis (Hook. & Wils.) Limpr. Ashland Co.: Basswood
Island. Bayfield Co.: Houghton; between Houghton Quarry
and Bayfield. Door Co.: Baileys Harbor. Grant Co.: Glen
Haven; Potosi. Outagamie Co.: near Readfield. Waukesha
Co. : Okauchee Lake.
T. tortuosa (Turn.) Limpr. Ashland Co.: Basswood Island.
Barron Co. : near Barron. Door Co. : Baileys Harbor ; Garret
Bay; Mud Bay.
Tortula
T. mucronifolia Schwaegr. Dane Co.: Madison. Iron Co.:
Montreal River. Marathon Co.: Knowlton. Racine Co.: Ra¬
cine.
T. rural is (Hedw.) Smith. Dane Co.: Madison. Door Co.:
Europe Bay. Grant Co. : Glen Haven ; Patch Grove ; Potosi.
Jefferson Co.: Palmyra. Sheboygan Co.: Cedar Grove.
Trematodon
T. ambiguus (Hedw.) Hornsch. Ashland Co.: Madeline Island.
Bayfield Co.: Drummond; Port Wing; between Port Wing
and Herbster. Lincoln Co.: Tomahawk. Oneida Co.: Noisy
Creek. Portage Co. : Stevens Point. Vilas Co. : Lac Vieux
Desert.
Ulota
U. CRISPA (Hedw.) Brid. Ashland Co.: Basswood Island. Bar¬
ron Co.: Barron Twp., sec. 35; Four Mile Swamp; Maple
Grove Twp., sec. 33. Bayfield Co.: Drummond; Herbster;
Mason; Roys Point, the old landing near Red Cliff. Dane
Co.: Madison. Door Co.: near Ellison Bay. Iron Co.: Mon¬
treal; along Montreal River. Lincoln Co.: Grandmother
Falls; near Grandmother Falls; between Nigger Island and
Tomahawk. Marathon Co.: Granite Heights. Oneida Co.:
near McNaughton; Rhinelander; along the Wisconsin River.
Rock Co.: Beloit. Vilas Co.: Lac Vieux Desert; along the
Wisconsin River.
Weisia
W. viridula Hedw. Barron Co.: Barron Twp., sec. 35. Dane
Co.: Madison. Grant Co.: Bagley; Beetown; Glen Haven;
224 Wisconsin Academy of Sciences, Arts and Letters
Millville; Potosi. Jefferson Co.: Palmyra. Lafayette Co. :
Fajrette. Lincoln Co.: between Grandfather Falls and Mer-
ril. Milwaukee Co.: North Milwaukee. Rock Co.: Beloit;
Clinton. Waukesha Co.: Foster’s Woods, Fox River as W.
viridula var. stenocarya Bry. Eur. ; Menonomee Falls ; Nash-
otah; Upper Nemahbin Lake; Okauchee Lake; Waukesha;
New Berlin Twp., sec. 19.
Zygodon
Z. viridissimus (Dicks.) R. Br. Grant Co.: Glen Haven.
NOTES ON WISCONSIN PARASITIC FUNGI. V.
H. C. Greene
In the course of routine checking of hosts in connection with
the study of fungi parasitic on plants in Wisconsin, occasional
herbarium specimens have been found to bear parasites which
had not been reported for the state. During the last twenty
years there have been thousands of accessions of phanerogamic
specimens in the Wisconsin section of the University of Wiscon¬
sin Herbarium. It seemed that a systematic search would prob¬
ably provide a considerable number of new records of parasitic
fungi for the state. A survey was made, and this series of notes
is in large part based upon the 75 additional hosts and 20 addi¬
tional species which were discovered, and are here reported,
together with other relevant material.
Between 1,200 and 1,300 species of fungi parasitic on plants
have been recorded in the writings of the late J. J. Davis, and
in these notes subsequently, as occurring in Wisconsin. More
than 60% of these belong to the Fungi Imperfecti, about 20%
to the Uredinales and Ustilaginales, about 10% to the Ascomy-
cetes, and 5% to the Phycomycetes, together with a small num¬
ber of other forms. These figures represent approximations
only, but serve to emphasize the preponderance of imperfects in
point of numbers of species. Davis' “Parasitic Fungi of Wis¬
consin," which is somewhat incomplete, lists about 1,100 host
species, but of course this has no particular correlation with the
number of fungus species, since some hosts harbor a variety of
parasites, and certain parasites, such as some powdery mildews
and rusts, may go to many hosts. About 125 new species and
varieties of plant parasitic fungi have been described from Wis¬
consin material, nearly all of them by Davis, in notes from the
University Herbarium.
Davis in his final publication, “Parasitic Fungi of Wiscon¬
sin," mentions Gleditsia triacanthos as a host of Microsphaera
alni. There is no report of this in any of his notes, and I find
no specimens in either the University Herbarium or the Davis
225
/
226 Wisconsin Academy of Sciences , Arts and Letters
Herbarium. However, Professor N. C. Fassett has recently col¬
lected a specimen of G. triacanthosy in the Sugar River bottoms
at Avon, Rock Co., which is profusely mildewed with M. ALNI,
and a portion of this is being entered as a mycological specimen.
Hydrophyllum appendiculatum from the vicinity of Viroqua,
Vernon Co., is heavily infected with the oidial stage of a pow¬
dery mildew, presumably Erysiphe cichoracearum DC.
Evonymus atropurpureus , which reaches the northern limit
of its range in Wisconsin, is frequently infected with oidium,
probably Microsphaera alni, but mature perithecia are not
formed.
Professor William Trelease in his “Preliminary List of Wis¬
consin Parasitic Fungi” records orchard grass ( Dactylis glom-
erata) as a host of Phyllachora graminis. Dr. C. R. Orton
has examined this specimen, at present in the collection of the
Missouri Botanical Garden, and states that as the result of very
careful comparison, he has reached the conclusion that the host
is undoubtedly Hystrix patula which is very commonly attacked
by Ph. graminis.
Dr. Orton finds that a specimen of Phyllachora on Panicum
virgatum , collected in October 1920 at Muscoda, Grant Co., has
spores and asci that correspond to those of Phyllachora gram¬
inis, although the specimen is somewhat ayptical in gross ap¬
pearance. The fungus rarely matures on this host, and this is
the only fully developed Wisconsin collection.
Phyllachora puncta (Schw.) Orton occurs on Panicum
sp. belonging to the section Depauperata, collected at Brodhead,
Green Co., in September 1926. The host is probably either Pani¬
cum perlongum or Panicum depauperatum. There are no pre¬
vious reports of Phyllachora on species belonging to this sec¬
tion.
On several occasions Mycosphaerella sp. has been observed
on spring flowering specimens of Clematis verticillaris, on the
more or less woody tendrils of the preceding season’s growth.
In the absence of proof to the contrary, however, it seems likely
that the fungus developed saprophytically.
In the fall of 1942 Mycosphaerella sp. occurred on the
leaves of Panicum implicatum in dead areas which contained
abundant pycnidia of what I have previously reported as Sep-
toria GRAMINUM Desm. It seems possible that the two are con¬
nected.
Greene— Notes on Wisconsin Parasitic Fungi. V. 227
Davis (Trans. Wis. Acad. Sci. 30: 14, 1937) noted the pres¬
ence of Mycosphaerella sp. destructively parasitic on the leaves
of Iris lacustris from Bailey's Harbor, Door Co., on the Lake
Michigan shore. A fungus which is microscopically identical,
and which affects the host in the same manner, has been found
on the overwintered leaves of Sisyrinchium graminoides , col¬
lected on a bluff above Lake Michigan in the vicinity of Port
Washington, Ozaukee Co. Since the latter collection was ob¬
served only on overwintered leaves, the parasitism of the fungus
remains to be demonstrated.
A parasite found in small quantity on living foliage of Po-
tentilla recta at Eagleville, Waukesha Co., July 2, 1941, appears
to belong to the genus Phaeosphaeria Miyake (Jour. Coll. Agr.
Tokyo 2: 246, 1910). Saccardo includes this under his subgenus
Leptosphaerella of the genus Leptosphaeria Ces. & DeNot.,
which differs from Eu-Leptosphaeria in that members of Lep¬
tosphaerella are aparaphysate and folicole. The perithecia are
epiphyllous on small white spots, the asci rather narrow, about
50 X 10/*. The ascospores are olivaceous, fusiform, triseptate,
about 20 X 4/x. This is obviously not Leptosphaeria minima
(Duby) Sacc. occurring on Potentilla argentea . The latter has
asci 50 X 20/a and biseptate spores, 20-25 X 6-7/*.
The species of Ribes in Wisconsin bearing uredia and telia of
Cronartium ribicola F. de Wal. do not appear to have been
fully enumerated in earlier notes. There are specimens in the
University Herbarium on Ribes americanum , R. cynosbati, R.
grossularia, R. hirtellum, R. nigrum , R. prostratum , and R.
triste. Specimens labelled as being on Ribes oxyacanthoides have
been referred to R. hirtellum. Blister rust occurs in all the
northern counties.
Although Coleosporium solidaginis is frequently and con¬
sistently found on a number of species of Solidago and Aster in
Wisconsin, certain other species are not attacked. C. solidaginis
has been observed on 14 species of Solidago and 18 species of
Aster as follows : Solidago altissima, S. canadensis , S. castrensis ,
S. glaberrima, S. hispida, S. latifolia, S. nemoralis, S. patula ,
5. riddellii, S. sciaphila*, S. serotina, S. speciosa , S. uliginosa ,
S. ulmifolia; Aster azureus , A. cordifolius, A. ericoides, A. junci-
formis , A. laevis, A. lateriflorus , A. lindleyanus* , A. lucidulus,
A. macrophyllus, A. novae-angliae, A. novi-belgii, A. oblongi-
228 Wisconsin Academy of Sciences, Arts and Letters
folius, A . paniculatus var. simplex ( A. tradescanti) , A. pilosus,
A. prenanthoides, A. puniceus, A. sagittifolius , and A. umbella-
ius . Where an asterisk follows the name it indicates that the
fungus is not represented by a specimen in the Cryptogamic
Herbarium, but has been observed on phanerogamic specimens
in the University Herbarium.
Davis found Ravenelia epiphylla (Schw.) Diet. II, III on
Tephrosia virginiana at Muscoda, Grant Co., in 1934. In his
“Parasitic Fungi of Wisconsin,” p. 41, he states that this was
likely introduced, since the focus of distribution was along the
railroad right of way, and he offers the suggestion that suc¬
cessive hot summers may have been a factor in its introduction
from farther south. That such is probably not the case is indi¬
cated by the fact that uredia of R. epiphylla have been noted on
a phanerogamic specimen of Tephrosia virginiana which was
collected in 1894 at Petenwell Rock near Necedah in Juneau Co.,
a locality which is 60 miles north of Muscoda. Since Petenwell
Rock is at least 2 miles from a railroad it seems unlikely that the
fungus was introduced there by that agency. Uredia also occur
on another phanerogamic specimen collected in 1891 at Albany
in Green Co., about 35 miles south of Muscoda. Thus, it would
appear that Ravenelia epiphylla has quite possibly been con¬
tinuously in the state.
Pycnia which, in all likelihood, are those of Uromyces hal-
stedii DeToni occur in circular amphigenous clusters on the
leaves of a specimen of Trillium cernuum var. macranthum col¬
lected near Stanley in Clark Co., but in the absence of aecia
a new record seems scarcely warranted. The fungus has been
reported only on Trillium grandiflorum in Wisconsin, and is not
listed on T. cernuum in Arthur's Manual.
Eriophorum viridi-carinatum which was recorded as a host
for Puccinia ANGUSTATA Peck in Wisconsin should be dropped,
for it has since been shown that the host plant, which was pre¬
served along with the rust collection, is Eriophorum virginicum.
Uredia of Puccinia extensicola Plowr. have been found on
a specimen of Car ex aenea Fernald (C. foenea var. aenea) col¬
lected at Port Wing, Bayfield Co., July 9, 1897 by L. S. Cheney
(Host det. by K. Mackenzie). P. extensicola is reported by
Arthur (N. Amer. Flora 7(1) : 362) as occurring on this host
in Wisconsin, but Davis, so far as I have been able to determine,
Greene — Notes on Wisconsin Parasitic Fungi . V. 229
does not mention it, nor do I find any specimens in the Univer¬
sity Herbarium or in the Davis Herbarium.
In 1938 aecia of what is presumably Uromyces silphii
(Burr.) Arth. (U. junci-tenuis Syd.) were collected at Madison
in profuse development on Helianthus strumosus. There is a
single earlier collection on the same host. The small spores serve
to distinguish this from Puccinia helianthi, but not from
Uromyces junci. Since the latter is not known to occur in Wis¬
consin, it seems probable that these are, as stated, the aecia of
U. SILPHII.
Uromyces silphii (Burr.) Arth. Ill occurs on a collection
of J uncus dudleyi from Washburn Co., Minong, September 6,
1928, and also from Rock Co., Footville, October 25, 1936. A
lone earlier collection is from Wausaukee in Marinette Co.
Davis in his “Third Supplementary List of Parasitic Fungi
of Wisconsin” (Trans. Wis. Acad. Sci. 14(1) : 101, 1903) re¬
cords Cypripedium pubescens , from Somers, Kenosha Co., as a
host of Puccinia cypripedii Arth. & Holw. In a later collection
from Gays Mills, Crawford Co., the same host is entered as
Cypripedium parviflorum var. pubescens in accordance with the
then usage, but in his “Provisional List” and in his “Parasitic
Fungi of Wisconsin” he lists Cypripedium parviflorum as the
host. There are in the Cryptogamic Herbarium only these two
collections from the state, both plainly on what certain authori¬
ties have called the var. pubescens. The most reliable present-
day opinion is that Cypripedium pubescens and C. parviflorum
are distinct and well-marked species. (See Fuller, A. M., Bull.
Publ. Mus. Milwaukee 14(1) : 64-70, 1933). Cypripedium parvi¬
florum, therefore, should be deleted as a host of Puccinia cypri¬
pedii in Wisconsin. The fungus has also been found on a speci¬
men of C. pubescens from the vicinity of Ashland, Ashland Co.,
collected by L. S. Cheney in July 1896, thus much extending the
range over the two southern stations cited above.
Puccinia jussiaeae Speg. I on Ludvigia polycarpa was col¬
lected once by Davis in the Wisconsin River bottoms, at Blue
River in Grant Co. Another specimen has been discovered on
the same host from the Mississippi River bottoms, opposite Du¬
buque, la., also in Grant Co.
Puccinia tumidipes Peck II, III has been found in profuse
development on a specimen of Lycium halimifolium collected at
230 Wisconsin Academy of Sciences , Arts and Letters
Appleton, Outagamie Co., in September 1928. There is a single
scanty earlier collection from Madison on this same host.
Puccinia hyssopi Schw. occurs on Agastache scrophulariae-
folia from Fall Creek, Eau Claire Co. The one previous collec¬
tion is from Viroqua, Vernon Co. On the upper leaf surface,
above each telial sorus, there are definite spots bearing what
appear to be perithecia of Phaeosphaeria, mostly immature and
very probably developed saprophytically following the rust.
Pestalotia sp. has been seen on spots on the leaves of Hy¬
pericum kalmianum from Sauk Co., but it seems improbable that
the fungus developed parasitically.
Coniothyrium insitivum Sacc. has been found on the stem
of a specimen of Berberis vulgaris collected in the vicinity of
Milwaukee in July 1837. (The specimen is from the herbarium
of the noted Wisconsin naturalist, I. A. Lapham.) This may
have been parasitic for it is deeply seated in the portion of the
stem bearing the current year's foliage.
An examination of specimens of Septoria coptidis B. & C.
on Coptis trifolia in the Cryptogamic Herbarium shows very
narrow sporules (l/i or less) which run from 15 to 65/a long, the
range being fairly small for any one specimen, e. g., 40-60/x,
30-50/a, 25-35 /a, 15-25/a. The lesions are all very similar, and it
seems reasonable to suppose that this is the organism described
by Berkeley and Curtis, but the spore length is seen to be far
more variable than the arbitrary 25/a indicated by them.
In August 1938 S. Fogelberg made a collection of Septoria
cephalanthi Ell. & Kell, on Cephalanthus occidentalis at Blue
River, Grant Co. This species must be very rare, for the Blue
River locality was intensively worked by Davis, over a period of
many years, without finding it. He made one collection in 1901
in Kenosha Co.
Ellis and Bartholomew described Septoria grindeliae on
Grindelia squarrosa and issued specimens (with description on
label) as No. 1874 of Ellis and Everhart's Fungi Columbiani.
Their description is as follows: “Spots round, whitish at first,
becoming brown, mm* in diam., with a narrow, raised
darker colored border. Perithecia epiphyllous, partially erump-
ent, mostly visible also on the under side of the leaf, few, often
only one, in the center of the spot. Sporules slightly curved, con-
Greene — Notes on Wisconsin Parasitic Fungi . V. 231
tinuous or obscurely septate (?), 40-60 X 2*4 micr., a little
thicker at one end. The leaves become brown and dead.” Sep-
toria sp. has been found on a specimen of the same host collected
near Plover in Portage Co. It is quite different from S. GRIN-
deliae in that there are no definite spots, merely brown, dead
areas, and in having sporules that are markedly curved, closely
and distinctly septate, about 30-45 X 2/x, and not thicker at one
end. Unfortunately the material is not sufficient to constitute a
type specimen, but a slide has been preserved for future refer¬
ence.
Seftoria collected on leaves of Solidago serotina , May 26,
1942 at Eagleville, Waukesha Co., is assigned to Septoria fumo-
SA Peck. As Davis pointed out (Trans. Wis. Acad. Sci. 19(2) :
705, 1919) the classification of Septoria on Solidago is in an un¬
satisfactory state, but the specimen in hand fits Peck's descrip¬
tion quite closely. Davis indicated that in his opinion Septoria
davisii, also on Solidago, is probably not distinct from S. FU-
MOSA.
Botrytis sp. occurs profusely on the leaves of Ranunculus
rhomboideusy collected at Portage, Columbia Co. In an earlier
publication (Trans. Wis. Acad. Sci. 32: 78, 1940) I reported
Botrytis sp. on Ranunculus abortivus. Davis, in describing the
occurence of Ascochyta infuscans Ell. & Ev. on the latter host
(Trans. Wis. Acad. Sci. 16(2) : 757, 1910) states “The effects
of this parasite upon the host are serious, causing speedy death
of as much of the plant as is distal to the point of attack and in
moist weather such dying portions are usually covered by a
growth (Botrytis as I have seen it) that seems to inhibit the
development of the pycnidia, so that it is only in comparatively
dry weather that I have been able to get satisfactory specimens.”
There is no trace of Ascochyta in either of the specimens men¬
tioned above, but it seems quite possible that the primary infec¬
tion may have been due to Ascochyta infuscans, as suggested
by Davis.
Ramularia multiplex Peck occurs on a specimen of V ac¬
tinium macrocarpon from Fall Creek, Eau Claire Co. A single
previous collection on this host was made at Gaslyn, Burnett Co.
in 1911. This is likely more common than the lack of specimens
would indicate, since the host is extensively cultivated in Wis¬
consin.
232 Wisconsin Academy of Sciences, Arts and Letters
Ram ul aria diervillae Peck was found on Diervilla lonicera
near Mt. Vernon, Dane Co., in June 1938. This is the first col¬
lection from southern Wisconsin. Earlier specimens are from
the central counties of Marathon, Waushara, and Sheboygan.
Cladosporium sp. has been found in a seemingly parasitic
development on the aecial cups of Tranzschella pruni-SPINO-
SAE (Pers.) Diet, on Hepatica acutiloba , collected at Madison in
May, 1938. However, since the material is scanty, and there are
apparently no previous reports of Cladosporium on uredinace-
ous hosts, no attempt is here made to determine the specific iden¬
tity.
Well developed Cladosporium appears on a dried specimen of
Astragalus canadensis from Lynxville, Crawford Co. It may be
that the fungus developed while the bulky specimen was in press.
Heterosporium sp. occurs on a specimen of Luzula salutensis
from Hogarty, Marathon Co. Coll. N. C. Fassett, May 21, 1932.
This is perhaps closely allied to Heterosporium magnusianum
Jaap (occurring in Europe on Narthecium/ossifragum of the
Liliaceae), but seems set apart by the darker, more pronouncedly
geniculate conidiophores. The conidia are very similar. I do not
find any reports of Heterosporium on Juncaceae. The material
in hand is, however, insufficient for more extensive study.
Panicum boscii Poir. has been reported as a host for Cerco-
spora fusimaculans Atk. (C. panici J. J. Davis) in Wisconsin,
but it now appears that such reports should be referred to Pam-
cum latifolium , since P. boscii , according to the best available
information, does not occur in Wisconsin.
Cercospora gei Fckl. was found on a specimen of Geum tri-
florum from Searl’s Prarie, Juneau Co., (T19N R4E S5). This
is the second Wisconsin station for this uncommon fungus.
Lespedeza violacea from Potosi, Grant Co., bears Cercospora
lespedezae Ell. & Dearn. A single earlier collection on this rare
host is from Glen Haven, Grant Co.
A scanty collection of Cercospora sp. was made on Oxy polis
rigidior in the vicinity of Troy Center, Walworth Co. A slide
was prepared and submitted to Professor Chupp who believes
that it may be a new species, since the conidiophores and conidia
are appreciably more narrow than those of CERCOSPORA POLY-
taeniae Ell. & Kell., or others with acicular conidia on hosts
closely related to Oxypolis. Description of the species must,
however, of necessity await collection of more ample material.
Greene— Notes on Wisconsin Parasitic Fungi . V. 233
It seems possible that Sclerotiomyces colchicus Worono-
ehin is identical with Sclerotium mendax Sacc. reported by me
on Solidago altissima. Davis (Trans. Wis. Acad. Sci. 24: 301,
1929) states “While fungous growths on 'honey dew’ on leaf sur¬
faces are not parasites their effects are probably ill. An inter¬
esting form that occurs in Wisconsin on the leaves of various
plants is apparently the one to which Woronochin gave the name
Sclerotiomyces colchicus (Ann. Mycol. 2U: 234). The orbicu¬
lar flattened sclerotia strongly resemble perithecia.” This has
also been found recently in heavy development on Aster azureus
collected by N. C. Fassett at St. Croix Falls, Polk Co. Other
specimens in the herbarium are on Carya cordiformis and Ely -
mus virginicus. In their “Genera of Fungi” Clements and Shear
do not recognize Sclerotiomyces because of the lack of a gen¬
eric diagnosis, and they conclude that it is “apparently a sclero¬
tium.”
Additional Hosts
Albugo Candida (Pers.) 0. Ktze. on Lepidium apetalum.
Washburn Co., Chittamo, June 20, 1929. Coll. N. C. Fassett.
PERONOSPORA CORYDALIS DeBary on Corydalis sempervirens.
Ashland Co., Marengo, May 14, 1931. Coll. Wesley Warvi.
Peronospora calotheca DeBary on Galium tinctorium (G.
daytoni of Gray’s Manual). Sauk Co., LaValle, September 5,
1927. Coll. J. J. Davis. A specimen of this same fungus on
Galium trifidum from Blue River, Grant Co., June 15, 1935, col¬
lected by Davis and Greene has not hitherto been recorded.
Bremia lactucae Regel has been found on specimens of
Serinia oppositifolia collected by Delzie Demaree at Monticello,
Drew Co., Ark., May 2, 1941. Although not a Wisconsin collec¬
tion, this is recorded since Serinia is, so far as I am aware, a new
host genus for B. lactucae.
Specimens distributed from the University of Wisconsin
Herbarium as Uncinula negator (Schw.) Burr, on Psedera
quinquefolia , Gibraltar Rock, Columbia Co., Wis., August 13,
1940, are probably on Parthenocissus vitacea ( Psedera vitacea) ,
since it seems that P. quinquefolia is found in Wisconsin only as
an escape from cultivation.
Microsphaera diffusa Cke. & Peck on Symphoricarpos occi -
dentalis Pierce Co., Prescott, August 30, 1927. Coll. N. C. Fas-
234 Wisconsin Academy of Sciences , Arts and Letters
sett. In this collection the appendages are quite short, but as is
usual in this species, the ultimate tips of the branchlets are
straight, and not recurved as in Microsphaera almi.
Erysiphe polygoni DC. on Polygonum atlanticum. Milwau¬
kee Co., Milwaukee, September 2, 1939. Coll. L. H. Shinners.
Host det. by J. F. Brenckle. Perithecia not mature. On Poly¬
gonum buxiforme. Milwaukee Co., Milwaukee, August 4, 1939.
Coll. L. H. Shinners. Host det. by J. F. Brenckle. It appears that
most of the Wisconsin collections reported on Polygonum avicu *
lare should probably be referred to P. buxiforme.
Erysiphe cichoracearum DC. on Coreopsis palmata. Sauk
Co., Devils Lake, August 23, 1900. Coll. L. M. Umbach.
Erysiphe cichoracearum DC. on Aster lucidulus. Wauke¬
sha Co., Eagle, September 13, 1938. Coll. R. W. Pohl.
Phyllachora puncta (Schw.) Orton on Panicum euchlamy-
deum Shinners. Grant Co., Muscoda, October 5, 1920. Coll.
J. J. Davis. Host det. by L. H. Shinners.
Cronartium comptoniae Arth. II on Myrica gale. Bayfield
Co., Washburn, August 23, 1930. Coll. Newton Bobb. Not un¬
common on Myrica asplenifolia in Wisconsin.
Cronartium comandrae Peck II on Comandra richardsiana.
Ashland Co., Madeline Island, July 15, 1930. Coll. Newton Bobb.
Arthur's Manual reports C.COMANDRAE on Comandra livida from
Wisconsin. Presumably there is a specimen in the Arthur Her¬
barium. There is no specimen at the University of Wisconsin.
Puccinia coronata Cda. II, III on Elymus canadensis. Dane
Co., Madison, August 24, 1942. Coll. & det. by C. G. Shaw. Ar¬
thur reports the rust on this host from Saskatchewan only.
Puccinia andropogonis Schw. I on Penstemon grandiflorus .
Polk Co., Osceola, June 13, 1927. Coll. Mrs. Henry Arndt, Jr.
Puccinia extensicola Plowr. II, III on Carex scoparia. Polk
Co., Dresser Junction, September 4, 1927. Coll. N. C. Fassett.
Host det. by K. Mackenzie. Also on specimens of the same host
from Dane and Bayfield Counties. On Carex crawfordii . Bay-
field Co., Iron River, September 1, 1928. Coll. N. C. Fassett.
Host det. by K. Mackenzie. Also on a specimen from Burnett
Co. On Carex convoluta. Trempealeau Co., Trempealeau, Au¬
gust 23, 1927. Coll. N. C. Fassett. Host det. by K. Mackenzie.
On Carex rosea. Polk Co., St. Croix Falls, September 3, 1927.
Greene — Notes on Wisconsin Parasitic Fungi . V. 235
Coll. N. C. Fassett. Host det. by K. Mackenzie. On Carex viridu-
la. Door Co., Bailey’s Harbor, September 24, 1932. Coll. N. C.
Fassett. On Carex chordorrhiza. Oneida Co., McNaughton, July
7, 1893. Coll. L. S. Cheney. Also on a specimen from Jefferson
Co.
Puccinia BOLLEYANA Sacc. II, III on Carex lupulina. Portage
Co., Meehan, August 28, 1938. Coll. J. W. Thomson.
Puccinia canaliculata (Schw.) Lagerh. Ill on Gy perns
inflexus (aristatus of Gray’s Manual). Dunn Co., Elk Mound,
October 14, 1939. Coll. N. C. Fassett.
Puccinia eleocharidis Arth. Ill on Eleocharis smallii.
Washburn Co., Sarona, September 14, 1935. Coll. N. C. Fassett.
Uromyces silphii (Burr.) Arth. II, III (U/junci-tenuis
Syd.) on J uncus halticus var. littoraiis. Adams Co., Big Springs,
July 24, 1932. Coll. N. C. Fassett. Det. G. B. Cummins. Arthur’s
Manual cites an extensive list of localities in which Uromyces
JUNCl (Desm.) Tul. has been collected on J uncus balticus, but
does not list it as a host for U. silphii.
Uromyces silphii (Burr.) Arth. II, III on J uncus interior.
Iowa Co., Arena, October 3, 1925. Coll. N. C. Fassett. Also on
specimens from Trempealeau and Buffalo Counties. II on Jun-
eus brevicaudatus. Vilas Co., Plum Lake, Land-o-Lakes, Sep¬
tember 12, 1942. Coll. N. C. Fassett. Det. G. B. Cummins.
Specimens of Uromyces holwayi Lagerh. labelled as having
been collected on Lilium canadense and L. superbum in Wiscon¬
sin should all be referred to Lilium michiganense since the two
plants first mentioned apparently do not occur in this state.
Puccinia anemones-virginianae Schw. on Anemone ri-
paria. Grant Co., McCartney, July 21, 1932. Coll. N. C. Fassett.
Davis in his “Parasitic Fungi of Wisconsin” does not list
Anemone virginiana as an aecial host for Puccinia RUBIGO-vera.
Earlier collections of aecia on this host were in some doubt as to
identity (see Trans. Wis. Acad. Sci. 21: 259, 1924), but Davis
and this writer in July 1935 at Fish Creek, Door Co., made a
collection of indubitable P. RUBIGO-VERA on Anemone virginiana ,
and the latter is therefore listed here as a Wisconsin host.
Puccinia menthae Pers. II on Mentha citrata (cult.). Grant
Co., Ellensboro, September 2, 1930. Coll. N. C. Fassett.
Uromyces peckianus Farl. I on Plantago purshii. Grant
236 Wisconsin Academy of Sciences, Arts and Letters
Co., Muscoda, June 26, 1920. Coll. J. J. Davis. Closely associated
with the aecia are pycnidia of Septoria plantaginea var.
PLANTAGINIS-MA J ORIS Sacc.
Gymnosporangium clavipes Cke. & Peck I on fruit of Ame-
lanchier laevis X humilis. Ashland Co., Madeline Island, July
15, 1930. Coll. Newton Bobb. Host det. by E. L. Nielsen.
Gymnosporangium globosum Farl. I on Crataegus succw-
lenta. Dane Co., Madison, September 17, 1895. Coll. R. H. True.
On Crataegus punctata. Milwaukee Co., Cudahy, September 19,
1940. Coll. L. H. Shinners. On Crataegus holmesiana. Milwau¬
kee Co., Cudahy, September 19, 1940. Coll. L. H. Shinners. On
Crataegus calpodendron. Milwaukee Co., Whitefish Bay, Sep¬
tember 22, 1940. Coll. L. H. Shinners. Hosts det. by E. J. Pal¬
mer and L. H. Shinners.
Asteromella andrewsii Petr, on Gentiana flavida. Green
Co., Browntown, September 24, 1926. Coll. J. J. Davis.
Fernald (Rhodora 19: 147, 1917) differentiates Gentiana
clausa from G. andrewsii. It appears that both are in Wisconsin,
and probably Asteromella andrewsii and Puccinia gentianae
occur on both, although previously recorded only on G. andrew¬
sii.
Phyllosticta decidua Ell. & Kell, on Nepeta cataria. Ver¬
non Co., Viroqua, July 20, 1929. This ubiquitous and rather
dubious parasite has been collected in Wisconsin on the follow¬
ing diverse hosts which do not seem to have been listed in full
elsewhere: Agrimonia gryposepala , Agrimonia striata , Aralia
racemosa, Armoracia rusticana , Bidens frondosa, Cynoglossum
officinale , Eupatorium perfoliatum, Eupatorium sessilifolium,
Galeopsis tetraheit , Geum canadense, Hieracium aurantiacum ,
Humulus lupulus Lactuca canadensis , Lappula virginiana, Leon -
urns cardiaca, Ly copus uniflorus, Mentha arvensis var. canaden¬
sis , Monarda punctata , Nepeta hederacea, Rudbeckia hirta , Scu¬
tellaria latemflora, Stachys palustris, Stachys tenuifolia , Steiron-
ema ciliatum , Vernonia fasciculata and Veronica virginica.
Ascochyta graminicola Sacc. on Schizachne purpurascens
(Melica striata of Gray's Manual). Vilas Co., Trout Lake, July
2,1935. Coll. J. T. Curtis.
Stagonospora meliloti (Lasch) Petr, on Medicago lupulina.
Dane Co., Madison, July 15, 1937. Coll. & det. by F. R. Jones;
Greene — Notes on Wisconsin Parasitic Fungi. V. 237
Iowa Co., Blue Mounds, July 28, 1938. Coll. & det. H. C. Greene.
Septoria graminum Desm. on Panicum scribnerianum.
Dunn Co., Fall City, October 14, 1939. Coll. L. H. Shinners. On
Panicum tsugetorum. Juneau Co., Necedah, June 18, 1936. Coll.
F. Hamerstrom. On Panicum euchlamydeum Shinners. Pierce
Co., Bay City, August 29, 1927. Coll. N. C. Fassett ; Marquette
Co., Montello, June 20, 1938. Coll. N. C. Fassett.
Septoria caricinella Sacc. & Roum. on Carex cristata.
Brown Co., Green Bay, July 19, 1887. Coll. H. J. Schuette. On
Carex muhlenbergii. Jackson Co., Millston, September 28, 1935.
Coll. J. J. Davis.
Septoria polygonorum on Polygonum lapathifolium seems
not to have been reported. There is a specimen in the herbarium
from Port Wing, Bayfield Co. collected by Davis in September
1923. The fungus has also been found on other specimens of this
host from Ashland, Buffalo, Burnett, Dane, Kenosha, Sawyer
and Walworth counties.
Septoria dimera Sacc. on Silene latifolia. Door Co., Bailey's
Harbor, August 1, 1939. Coll. L. H. Shinners. This is a very
distinctive species, hitherto reported, so far as I am aware, only
on Silene nutans in Europe and on S . antirrhina in Wisconsin.
Septoria hepaticae Desm. on Hepatica americana. ( H . tri¬
loba of Gray's Manual). Walworth Co., Lauderdale Lakes, Town
of Sugar Creek, April 20, 1938. Coll. Douglas Wade.
Septoria ribis Desm. on Ribes missouriense . Dane Co., Mad¬
ison, October 8, 1942. Previous reports of this fungus on Ribes
oxyacanthoides should be referred to R. hirtellum.
Septoria agrimoniae-eupatoriae Bomm. & Rouss. on Agri-
monia pubescens (A. mollis of Gray's Manual). Sauk Co., Dev¬
il's Lake, August 8, 1913. Coll. J. J. Davis. This was placed in
the herbarium as A grimonia parvifloraf a species which it is now
believed does not occur in Wisconsin. The specimen was later
redetermined as A. mollis .
Septoria astragali Desm. on Lathyrus japonicus var. gla-
ber (L. martimus of Gray's Manual). Ashland Co., Oak Island,
July 27, 1936. Coll. Edith Seymour Jones. Trelease first re¬
ported this on Vida americana in Wisconsin, and Davis many
years later made a collection on the same host. Davis' remarks
on his specimen (Trans. Wis. Acad. Sci. 24: 298, 1929) apply
238 Wisconsin Academy of Sciences , Arts and Letters
without alteration to the present collection, and are as follows:
“In this collection the pycnidia are very imperfect and the
sporules grow out to a length of 120-200/x resembling Cylindro-
spcrmra.”
Septqria nolitangere Thum. on Impatiens pallida. Grant
Co., Wisconsin River bottoms opposite Bridgeport, September
15, 1930. Coll. N. C. Fassett; Grant Co., Wyalusing State Park,
August 15, 1938. Coll. S. Fogelberg.
Septoria campanulae (Lev.) Sacc. on Campanula rapuncu-
loides. Winnebago Co., Waukau, July 4, 1941. Coll. L. H. Shin-
ners. This appears to have been previously reported only on
Campanula americana and on C. aparinoides. Oudemans does
not list it as occurring on C. rapunculoides in Europe.
Ramularia urticae Ces. on Urtica procera. This fungus is
abundant on Urtica in Wisconsin and has previously been re¬
ported on Urtica gracilis. I have found it on several phanero¬
gamic specimens labelled Urtica procera. The distinction be¬
tween Urtica gracilis and so-called U. procera seems tenuous in¬
deed.
Ramularia occidentalis Ell. & Kell, on Rumex acetosella.
Sheboygan Co., Terry Andrae State Park, June 30, 1925. Coll.
A. M. Fuller.
Cladosporium astericola J. J. Davis on Solidago caster en-
sis. Juneau Co., Mauston, September 1935. Coll. B. O. Dodge.
Host det. by L. H. Shinners.
Passalora fasciculata (C. & E.) Earle on Euphorbia glyp-
tosperma. Portage Co., Plover, August 23, 1917 ; Shawano Co.,
Shawano, September 1, 1921. Coll. J. J. Davis as on Euphorbia
sp. indet. Host det. by N. C. Fassett.
Cercospora sagittariae Ell. & Kell, on Sagittaria anfolia.
Shawano Co., Shawano, September 1, 1921. Coll. J. J. Davis.
Placed in the herbarium, but not reported. The host determina¬
tion is confirmed from fruiting material present with the speci¬
men.
Cercospora caricina Ell. & Dearn. on Car ex crawfordii.
Dane Co., Sun Prairie, July 16, 1932. Coll. N. C. Fassett. In
this specimen the multiseptate conidia are long and very slender,
up to 100 X 2.5-3 ixf the conidiophores short, mostly about 15^.
On Car ex convoluta. Trempealeau Co., Trempealeau, August 23,
Greene — Notes on Wisconsin Parasitic Fungi . V. 239
1927. Coll. N. C. Fassett. Host det. by K. Mackenzie. On Carex
projecta. Oneida Co., Newbold, July 13, 1893. Coll. L. S. Cheney.
Cercospora comandrae Ell. & Dearn. on Comandra richard -
siana. Ashland Co., Madeline Island, July 15, 1930. Coll New¬
ton Bobb. Davis has reported C. comandrae on Comandra um¬
bellata. Concerning the former host, Beam in his “Flora of In¬
diana” states in part “ _ ... _ he (M. L. Fernald) says
that all of my specimens and all of those in the Gray Herbarium
from west of the Allegheny Mountains belong to this species
( C . richardsiana) . It is undoubtedly separated from Comandra
umbellata and in Britton and Brown, Illus. Flora, ed. 2, it was
regarded as a synonym. Fernald gives the range of Comandra
umbellata as restricted to the area east of the Allegheny Moun¬
tains.” It is possible therefore that Wisconsin fungi reported on
Comandra umbellata should all be referred to C. richardsiana .
Cercospora nasturtii Pass, on Berteroa incana. Waupaca
Co., Weyauwega, July 9, 1933. Coll. J. J. Davis. The spots, while
small, are fairly numerous and the fungus is mature.
Cercospora zebrina Pass, on Trifolim agrarium. Eau Claire
Co., Fall Creek, July 18, 1928. Coll. Helen F. Kunz.
Cercospora altheina Sacc. on Hibiscus trionum. Iowa Co.,
Avoca, September 10, 1923. Scanty. Coll. E. M. Gilbert and
J. J. Davis.
Cercospora senecionicola J. J. Davis on Senecio balsami-
tae. Forest Co., Laona, July 15, 1915. Coll. J. J. Davis. Davis
(Trans. Wis. Acad. Sci. 30: 10, 1937) described CERCOSPORA
senecionicola n. sp. on Senecio aureus. In the description it is
stated that the spots are indeterminate. The specimen on Sene¬
cio balsamitae was originally placed in the herbarium as Cerco¬
spora emaculata n. sp., but this was not published, perhaps be¬
cause of the small size of the specimen. Davis redetermined it,
presumably after description of the new species, but neglected to
record it.
Graphiothecium vinosum J. J. Davis on Ribes prostratum.
Wood Co., Dexterville, August 31, 1917. Coll. J. J. Davis. Davis
described this fungus on Ribes americanum (Trans. Wis. Acad.
Sci. 18(1) : 90, 1915). It is admittedly highly variable, and per¬
il aps doubtfully parasitic. The specimen on Ribes pro stratum
was set aside by Davis for study, but for some reason was over-
240 Wisconsin Academy of Sciences , Arts and Letters
looked. It appears to me to be but a somewhat slender version
Of G. VINOSUM.
Additional Species
In a study of soil fungi of Wisconsin, Mr. C. W. Hesseltine
has found Piptocephalis sp. and Syncephalis spp. parasitizing
Mucors in culture.
Phyllachora on Paspalum stramineum, collected by N. C.
Fassett at Cassville, Grant Co., September 11, 1930, has been
identified by Dr. C. R. Orton as Phyllachora wilsoni sp. nov.
Elsinoe ledi (Pk.) Zeller on Ledum groenlandicum. Douglas
Co., Gordon, July 18, 1907. Coll. J. J. Davis. Peck’s description
of this interesting ascomycete is as follows: “Spots orbicular,
grayish white, surrounded by a brown or purplish brown bor¬
der; perithecia epiphyllous, few on a spot, elliptic or oblong,
often substellately lobed by confluence, erumpent, black, context
whitish ; asci obovate or subglobose ; spores ovate or oblong, con¬
tinuous, at length uniseptate, 12-15/t long, 6-8At thick.”
Belqndidium juncisedum (Karst.) J. Lind, occurs on a
specimen of Juncus balticus var. littoralis from Oakland, Bur¬
nett Co. Coll. W. T. McLaughlin, August 19, 1929. Whether this
is actively parasitic is doubtful. Although it occurs on the cur¬
rent season’s growth, it is in an area that is entirely dead, and
whether death was due to this organism or to some other cause
is not known.
Uromyces glycyrrhizae (Rab.) Magn. I, III on Glycyr-
rhiza lepidota. Pierce Co., stony shore of Lake St. Croix, August
3, 1934. Coll. N. C. Fassett. This is of interest in that both host
and parasite are essentially western forms. Arthur’s Manual
gives the range of U/glycyrrhizae as North Dakota to Alberta,
southward to New Mexico and southern California.
Puccinia CAULICOLA T. & G. II, III on Salvia lanceolata.
Kenosha Co., 1 mi. S. of Racine Co. line, October 6, 1940. Coll.
N. C. Fassett, L. H. Shinners and S. C. Wadmond. In Arthur’s
Manual the range of this rust is given as South Dakota to Texas
and New Mexico; also in Mexico.
A fungus appearing parasitic on twigs of Morns rubra from
Bridgeport, Crawford Co., is referred to Phoma moricola Sacc.
The spore characters correspond well, the conidia being about
7-10 X 2-2.5/x hyaline, straight, and more or less biguttulate.
Greene — Notes on Wisconsin Parasitic Fungi . V. 241
In the report of the New York State Botanist for 1915, p. 37,
Phoma longipes B. & C. is listed as occurring on Morus alba.
It is stated that this was cited earlier as Phoma moricola Sacc.
by Burnham and Latham (Torreya 14: 210, 1914). It has not
been possible to obtain material for comparison with the Wis¬
consin collection. Dr. House informs me that the specimen in
Question is not in the New York State Herbarium.
Septoria aciculosa Ell. & Ev. on Fragaria virginiana. Wau¬
shara Co., Hancock, May 21, 1940. Coll. Max Partch. This was
found on overwintered leaves still attached to the plant. There
seems little doubt that the fungus developed during the previous
growing season.
Septoria canadensis Peck on Gornus canadensis. Oconto
Co., Keshena, June 22, 1934. Coll. E. E. Honey. The very slen¬
der sporules do not exceed 25 /* in length. Apparently distinct
from Septoria cornicola Desm.
Septoria pentstemonis Ell. & Ev. on Pentstemon digitalis .
Dane Co., Belleville, June 21, 1931. Coll. N. C. Fassett. Also on
specimens from Jackson and Outagamie counties. This species
differs from Septoria penstemonicola Ell. & Ev. (occurring in
Wisconsin on Pentstemon gracilis) in that the pycnidia are
borne on much more sharply delimited spots, and the sporules
are very short, mostly about 20/*, as opposed to 30-50/* in S.
pentstemonicola.
Septoria lanaria Fairm. on Antennaria parlinii. Vernon
Co., Ontario, May 9, 1931. Coll. N. C. Fassett. Also on Anten -
naHa fallax. Juneau Co., Necedah, May 22, 1932. A minute
form which Fairman (Ann. Mycol. 9: 151, 1911) described as
having sporules 23-33 X 1-1.5/*. In the Wisconsin specimens
many sporules are shorter than this. Fairman suggests that
S. lanaria may be a stage in the development of Mollisia
lanaria, described by him on Antennaria plantaginifolia.
Septoria mollisia Dearn. & House on Antennaria plantagi¬
nifolia. Iowa Co., Mineral Point, May 28, 1931. Coll. N. C.
Fassett. A well-marked species with the mature pycnidia widely
open, suggesting Mollisia. Dearness and House (New York
State Museum Bull. 188: 39, 1916) state “It may be questioned
whether the waxy appearing rim is a part of a true pycnidial
wall and whether the plant should not be called a Cylindro-
sporium ”
242 Wisconsin Academy of Sciences , Arts and Letters
Melasmia hypophylla (B. & Rav.) Sacc. on Gleditsia tri-
acanthos. Grant Co., Potosi, August 16, 1934. Coll. N. C. Fas-
sett.
Gloeosporium celtidis Ell. & Ev. on Celtis occidental is.
Grant Co., Millville, September 22, 1913. Coll. J. J. Davis. Davis
determined but did not report this. It appears possible that it is
but a weak parasite, since the leaves, as is usually the case with
Celtis late in the season, bear numerous insect galls. The spores
are decidedly fusoid, borne on rather long conidiophores, mostly
about 10-12 X 5/a.
Gloeosporium psoraleae Peck on Psoralea esculenta . Pierce
Co., Hager, August 25, 1935. Coll. N. C. Fassett. A very inter¬
esting fungus on a host that is extremely rare in Wisconsin.
The minute pustules are borne on blackish brown orbicular spots,
which are here amphigenous.
Cercospora copallina Cke. on Rhus copallina. Brown Co.,
Suamico, September 15, 1937. Coll. N. C. Fassett. In the past
this species has been distributed as Cercospora rhoina Cke. &
Ell. and as C. rhoina var. nigromaculans Peck. The fruiting
is definitely on the upper leaf surface, and the dense fascicles
are on a large black stroma which is from 50-125/a diam. The
variation from C. rhoina seems sufficiently great to warrant
specific differentiation.
Cercospora ludwigiae Atk. on Ludvigia polycarpa. Grant
Co., Mississippi River bottoms opposite Dubuque, la., August 31,
1930. Coll. N. C. Fassett. This corresponds very closely with
Atkinson's description, so there seems no doubt that it is the
same thing he found on Ludvigia alt erni folia in Alabama.
Cercospora isanthi Ell. & Kell, on Isanthus brachiatus.
Lafayette Co., Belmont, July 28, 1922. Coll. Huron H. Smith.
The round spots are very small, sordid whitish with a raised
margin. The conidiophores are rather poorly developed, but the
conidia are normal and are from 75-100 X 3-4/a as indicated in
the description.
Cercospora plantaginis Sacc. on Plantago sp. Dane Co.,
Madison, October 1, 1920. Coll. J. J. Davis and class. Referred
to this species with doubt at the time of collection and not re¬
ported. The determination is confirmed by Professor Chupp,
who regards Cercospora plantaginella Tehon as a synonym
Of C. PLANTAGINIS.
Greene — Notes on Wisconsin Parasitic Fungi . V. 243
Cercospora asterata Atk. on Aster lucidulus (A. puniceus
var. lucidulus of Gray's Manual). Waukesha Co., Eagleville,
September 14, 1941. In general, this conforms rather closely to
the fungus described by Atkinson, although the conidia are
slightly longer. Professor Chupp informs me that the type does
not have enough fruiting for satisfactory study.
NOTES ON WISCONSIN PARASITIC FUNGI. VI.
H. C. Greene
The fungi mentioned in this series of notes, unless otherwise
specified, were collected in the vicinity of Madison in 1943. Like
1942, 1943 was very favorable for the development of parasites
and a considerable number of new and rare species were found.
The rare Physoderma menyanthis DeBary occurred on
Menyanthes trifoliata near Eagleville in southwestern Waukesha
Co. Coll. July 5, 1941. A single earlier collection of this was
made by Davis in 1902 in Vilas Co.
Peronospora parasitica (Pers.) Fr. was found on Draba
caroliniana at Madison, May 1. Cheney found this on D. carotin -
mna at Madison in 1895, and Davis and I collected it in Columbia
Co., near Prairie du Sac, in 1935. The scarcity of specimens is
probably due to the fact that the host flourishes very early and
is largely overgrown by other foliage by the time most collectors
get into the field.
Peronospora trifoliorum DeBary was collected in some
abundance on Lupinus perennis at Hancock, Waushara Co., June
2, by Dr. B. M. Duggar. A single very scanty earlier specimen
on this host is from Millston, Jackson Co., taken in 1915 by
Davis.
Peronospora hedeomae Kell. & Sw. occurred on Hedeoma
hispida at Madison, June 15. The only previous station for this
on II. hispida is Blue River, Grant Co., where Davis and I col¬
lected it in 1935.
Tanacetum vulgare was heavily infected with the oidial
stage of a powdery mildew. Species of Erysiphe and Sphaero-
theca have been reported on this host in Europe. Aster linarii-
folius was similarly infected, presumably by Erysiphe cicho-
RACEARUM DC.
Capnodium sp. has been seen in abundant development on
Finns strobus from Stanley, Chippewa Co. Although this is per¬
haps not a parasite it is probably damaging to the pine, and is
245
246 Wisconsin Academy of Sciences , Arts and Letters
said to produce serious effects on the trees bearing it. Whether
this is identical with Capnodium pini B. & C., described on
“pine” from Maine is questionable.
As previously noted, Phyllachora boutelouae Rehm, so
far as observed, comes to maturity on Bouteloua curtipendula
in Wisconsin only after overwintering, and then but sparsely.
Leaves of this grass bearing the Phyllachora, from the previous
season, were collected and examined April 8. No asci with ma¬
ture spores were observed. Portions of a number of the leaves
were immersed in shallow water in a Petri dish and left at room
temperature for 48 hours. Fifteen ascomata from as many leaf
segments were then examined and all except one had matured.
Ascomata from dry leaves showed no further development. In
October leaves of the current season were treated in the same
fashion, but none of the uniformly immature ascomata showed
any change.
In the fall of 1942 several clumps of Panicum virgatum in
the University Arboretum were very heavily infected with sup¬
posed immature Phyllachora graminis. The clumps were
marked and collections made in the spring of 1943, but no furth¬
er development had taken place, and material placed in a moist
chamber failed to mature.
Cryptosporella anomala (Pk.) Sacc. on living shoots of
Corylus americana, May 21. Reported by Trelease, but there are
no interim Wisconsin collections in the herbarium. Concerning
this species Ellis and Everhart in “North American Pyrenomy-
cetes”, p. 531, state “The pustules appear first on the smaller
branches and are seriately arranged along one side of the
branch ; afterwards they appear also on the larger branches and
on the trunk itself, and in the course of two or three years the
part of the tree above ground is entirely killed. The roots, how¬
ever, still retain their vitality and continue to send up each year
a luxuriant growth of new shoots destined to be destroyed the
succeeding year by the inexorable pest.”
Entyloma compositarum Farl. occurred on Senecio aureus ,
June 30. It has been found once or twice before in Wisconsin on
this host, and on the basis of one of these collections Ciferri
(Ann. Mycol. 26: 40, 1928) set up the new species Entyloma
WISCONSINENSE which Davis does not consider to be distinct
from E. COMPOSITARUM.
Greene — Notes on Wisconsin Parasitic Fungi. VI. 247
Professor R. I. Evans has recently found among the manu¬
scripts of the late L. S. Cheney a packet bearing rusted leaves
of Betula pumila, collected in July 1906 at Bloomer, Chippewa
Co. This is the uredial stage of Melampsoridium betulinum
(Pers.) Kleb., rarely collected in Wisconsin and hitherto repre¬
sented in the herbarium by but a single specimen from the state.
Although the aecial stage of Coleosporium solidaginis
(Schw.) Thum. is probably not uncommon on Pinus banksiana
in Wisconsin it has seldom been collected. There are but three
satisfactory specimens, all recent, from Dane, Grant, and Adams
Cos. The lone collection on Pinus resinosa is from Grant Co.
If one may judge by the scarcity of material in the herbari¬
um, the aecial stage of Uromyces lespedezae-procumbentis
(Schw.) Curt, is rarely developed in Wisconsin. This was abun¬
dant on Lespedeza capitata in the University Arboretum in June.
Despite considerable previous collecting experience, over a pe¬
riod of years, in regions where the host is fairly common, I have
never before encountered aecia of this rust, although uredia and
telia are of course regularly produced.
Liatris pycnostachya was heavily infected by Puccinia
liatridis (Webber) Bethel in the University Arboretum in July.
The sole previous station for the rust on this host is near Eagle
in Waukesha Co. The source of the infection is a puzzle, for
there are no stands of rusted Koeleria cristata , the alternate
host, anywhere in the vicinity so far as I know.
Puccinia helianthi Schw. I has been found on Helianthus
strumosus , June 14. Trelease in 1885 reported aecia of this rust
on FI. strumosus , but early reports are questionable.
Puccinia hieracii (Schum.) Mart. II, III occurred in pro¬
fusion on Agoseris cuspidata, June 9. Professor N. C. Fassett
made a single small earlier collection on this rare host at Pine
Bluff, Dane Co.
Davis in 1893 reported Uromyces silphii (Burr.) Arth. I
(as Aecidium compositarum) on Silphium integrifolium from
Racine. There is, however, no specimen at the University of
Wisconsin. This was in great abundance on close plantings of
S. integrifolium in the University Arboretum in June; also found
on the Scuppernong Prairie near Eagle, Waukesha Co. in June.
Ellis and Everhart (Bull. Torr. Bot. Club 2J+\ 285, 1897) de¬
scribed Phyllosticta gallicola occurring on insect-produced
248 Wisconsin Academy of Sciences , Arts and Letters
galls which have been known as “Rhytisma solidaginis”. A
somewhat similar form has been found at Madison on poorly
developed galls on the leaves of Solidago latifolia (cult.). The
conidia of Ph. gallicola were described as being 6-15 X 6-8/*,
but those of the fungus on Solidago latifolia are 14-21 X 5-7/*.
It seems improbable that this is a parasite.
Darluca filum (Biv.) Cast, occurs on telia of Puccinia
ELEOCHARiDis on Eleocharis acicularis. In the great majority of
cases this parasite occurs on uredia only.
A fungus which is perhaps referable to Ascochyta was found
on leaves of Leonurus cardiaca, July 13. It is definitely not
Ascochyta leonuri Ell. & Dearn. In this specimen the spots
are rather large, angled, blackish brown, one or two to a leaf.,
The thin-walled pycnidia are about 100-130/*, or somewhat more
in diam. The conidia are quite variable with many of the larger
ones running 10-12 X 3.5-4/*, with a single median septatiouu
The shorter conidia are mostly about 5-6/* long, and continuous.
It may be that they are immature. At any rate the material does
not seem sufficiently well-defined to warrant description of a
new species without additional confirmatory specimens.
So-called “Davisiella” has been found in Phyllachora bob-
telouae Rehm on overwintered leaves of Bouteloua curtipen-
dula. The conidia are obscurely 3-septate, almost cylindrical,
tapering slightly at each end, mostly about 17-22 X 3/*. For
previous discussions of conidial forms associated with Phylla¬
chora see the following, all appearing in the Trans. Wis. Acad.
Sci.: Vols. 19(2): 701, 1919; 22: 166 (1926); 30: 7 (1937);
34: 86 (1942) ; 35: 116 (1943). In addition to Ph. boutelouae,
Ph. graminis, Ph. luteomaculata, Ph. puncta and Ph. vul-
CATA have been found bearing “Davisiella” in one or another
form.
Stagonospora caricinella Brun. collected on Carex Penn¬
sylvania, May 6, has spores some of which have as many 6
septations and are 27 X 5/*, while what is supposedly the same
species, found on a broad-leaved Carex on May 8, has spores
10-13 X 3-3.5/*, some of which are uniseptate, others continu¬
ous. Davis gives a rather extensive discussion of this form in
Trans. Acad. Sci. 18(1) : 264 (1915).
A fungus which is assigned to Stagonospora luzular
(West.) Sacc. was found on dead tips of leaves of Luzula saltw-
Greene— Notes on Wisconsin Parasitic Fungi, VL 249
ensis from Sauk Co. The hyaline conidia are mostly 2-septate,
guttulate, straight, 12-15 X 3/*. It is doubtful that this is para¬
sitic.
Septoria betulae (Lib.) West, and Septoria betulicola
Peck show a tendency to integrade and may not be specifically
distinct. A recent collection on Betula alba var. papyrifera has
rather small, angled spots with a ragged, incomplete dark brown
border and a light brown center on which the pycnidia are
borne. The spots are distinct and sharply defined, with the
pycnidia easily visible by transmitted light. The sporules are
about 30-40 X 2-2.5/*. This has been filed under S. betulae.
Davis discussed these forms at some length. (See Trans. Wis.
Acad. Sci. 18(1) : 102, 1915).
Aconitum novaboracense var. quasiliatum Fassett, collected
at Parfrey’s Glen, Sauk Co., July 30, 1929, bears a Septoria
which may be allied to Septoria lycoctoni Speg. Unfortunately
the areas with the Septoria are overrun with Colletotrichum so
that the character of the original spots cannot be determined.
The pycnidia are about 100/* diam., or slightly more, and the
slender continuous sporules 15-25 X 1/*. There are no previous
reports of fungi on this rare host.
Septoria lythrina Peck was found in profuse development
on Lythrum alatum, July 15. In 1910 Davis reported this from
Union Grove, Racine Co., but there is no specimen at the Uni¬
versity of Wisconsin.
A clean-cut and well-defined species of Septoria occurred in
small quantity on leaves of Gentiana procera, Lake Wingra
marsh, Madison, September. This is quite unlike S. GENTIANAE
Thum., S. gentianoides Dearn. & House, or S. microsora Speg.
The spots are gray with a distinct light tan border, rounded,
5 mm. diam. ; the large black pycnidia are gregarious, strongly
erumpent, their position being evident whichever side of the leaf
is inspected ; pycnidia 250-300/* diam. ; sporules hyaline, pluri-
septate, slender, about 40-50 X 1.5/*. This has filed temporarily
under Septoria sp., for the small size of the specimen precludes
its use as a type.
Previous collections of Septoria linariae Greene on Linaria
canadensis (see Trans. Wis. Acad. Sci. 35: 130, 1943) have been
notable for heavy infections of stems as well as leaves, but a
gathering made in early June 1943 shows pycnidia only on the
250 Wisconsin Academy of Sciences, Arts and Letters
tips of the lower leaves. Later specimens, however, show stems
infected, so it would appear that the leaves are first attacked.
The host is an annual and the presumption is that the infection
is seed borne.
Septoria campanulae (Lev.) Sacc. developed in some quan¬
tity on Campanula aparinoid.es in August. A single earlier col¬
lection on this host is from Spooner, Washburn Co., made by
Davis in 1911.
The report of Septoria davisii Sacc. (S. fumosa Peck) on
Solidago canadensis in Davis' “Parasitic Fungi of Wisconsin" is
in error as to host which should be Solidago altissima. (see Da¬
vis, Trans. Wis. Acad. Sci. 24: 281, 1929).
Until recently Septoria coreopsidis J. J. Davis has been
represented in the herbarium only by the type specimen collected
at Hixton, Jackson Co., in September 1917. This was found at
Madison on the same host, August 1943. Here the sporules,
which seem well-developed, are from 20-35/* long, instead of
30-50/* as in the type.
Davis reported Septoria krigiae Dearn. & House on the
scapes and involucral bracts of Krigia virginica. This is one of
the earliest of the spring flowering composites of the region and
Davis' material taken on June 20, represents but the dried re¬
mains of the plant and does not include the basal rosette which
had died away. A collection of the same parasite was made May
13 on the green basal leaves at Mazomanie, Dane Co.
A Septoria which appears to belong to the S. lactucae-
lactucicola group has been found in small quantity on leaves
of Agoseris cuspidata. The pycnidia are small, slightly less than
100/*, the conidia slender, straight, continuous, about 22-25 X
1.5/a. The identification can be only tentative in the lack of ample
material and seeming absence of previous reports of Septoria on
Agoseris.
Trelease in his preliminary list of Wisconsin parasitic fungi
reported Septoria sp. on leaves of Silphium integrifolium. This
was later reported by Davis as Septoria silphii Ell. & Ev., so I
suppose he checked the Trelease specimen, at present in the
herbarium of the Missouri Botanical Garden. Davis did not find
the fungus on this host, but it occurred in profusion on S. inte-
grifolinm in June in the University Arboretum. It seems to be
without question the same thing Trelease had, judging from his
short descriptive notes.
, Greene — Notes on Wisconsin Parasitic Fungi. VI. 251
Leptostroma pinastri Desm. (the conidial stage of Lopho-
dermium pinastri (Schrad.) Chev.) appears to be rarely de¬
veloped on Finns resinosa in Wisconsin. Out of many hundreds
of leaves examined, most of them with the perfect stage, I have
found but a single one bearing the Leptostroma. There are two
specimens on Pinus banksiana in the herbarium.
In Notes II (Trans. Wis. Acad. Sci. 34: 98, 1942) in connec¬
tion with Sporonema trifolii n. sp. it was stated “Apparently
it usually occurs in association with Ascochyta trifolii or
Gloeosporium trifolii. . . .” As should have been specified,
these names are synonyms of Stagonospora recedens (C. Mas-
sal.) Jones & Weimer. (see Jour. Agr. Res. 57: 791-812, 1938).
A perplexing form intermediate between Gloeosporium and
Colletotrichum, appearing parasitic, has been found on large,
deep brown, orbicular spots on leaves of Pyrola elliptica. The
acervuli are deeply seated in the host tissue, inconspicuous,
small, about 60-75/x diam., with pale brown setae which are
scarcely longer than the diameter of the acervulus. The conidia
are fusoid or short-cylindrical, mostly about 10 X 4/*, and are
of a type more commonly associated with Gloeosporium than
with Colletotrichum. Some of the acervuli lack setae, but since
the conidia are the same it appears that only a single fungus is
involved.
Bulblets of Allium tricoccum from Ridgeway, Iowa Co., bear
acervuli of Colletotrichum on the scales. This does not seem to be
Colletotrichum circinans, and it is difficult to say whether it
is parasitic. There is no admixture of any other of the common
saprophytes.
A fungus which is perhaps referable to Cylindrocephalum
Bon. occurs on languishing foliage of Caulophyllum thalictroides ,
collected at Blue Mounds, Iowa Co., August 13, 1938. Micro¬
scopically this is not unlike Cylindrocephalum hyalinum
(Cke. & Harkn.) Sacc. as described, although the conidia are
somewhat shorter. Occasional conidiophores are branched. It
is likely that this is parasitic, since it causes more or less definite
spotting in leaf areas which are still green.
Ramularia arvensis Sacc. developed abundantly on Poten -
tilla canadensis in June. This fungus is of course extremely com¬
mon on Potentilla norvegica var. hirsuta , but is usually not
found on P. canadensis.
252 Wisconsin Academy of Sciences , Arts and Letters
A species of Cladosporium has been collected on living leaves
of Lysimachia terrestris. There seem to be no reports of Clado¬
sporium on Primulaceae. This fungus is not morphologically
distinct from various other species of Cladosporium as described,
and it is felt that host relationship alone is insufficient to war¬
rant erection of a new species in this case.
Cladosporium astericola J. J. Davis has been collected on
Solidago speciosa on one previous occasion. The earlier specimen
is on leaf blades only, as is the case with specimens on other
hosts. In the recent collection, however, the fungus is princi¬
pally on the upper stem, forming small, rounded, well-defined
patches.
In a previous publication (Trans. Wis. Acad. Sci. 32: 81,
1940) I reported Cladosporium nervale Ell. & Dearn. on Eu¬
phorbia corollata. It no w appears that this was the dubious
Fusicladxum fasciculatum C. & E. (Passalora fasciculata
(C. & E.) Earle) . I was misled by the exceptionally long and lax
conidiophores in the specimen in question and by definite evi¬
dence of catenulation of the conidia. I believe that this organism
would be much better placed under Cladosporium, but refrain
from any action, since the proper position of the fungus has long
been in dispute. Davis reported Passalora fasciculata on
E. corollata from Racine in 1903, but there is no specimen col¬
lected by him on this host at the University of Wisconsin. I have
specimens from Madison and from the vicinity of Lodi, Colum¬
bia Co.
The report of Cercosporella filiformis J. J. Davis on
Thalictrum dasycarpum (Trans. Wis. Acad. Sci. 32: 80, 1940)
is plainly in error. This is Cylindrosporium thalictri Ell. &
Ev. which is probably not a good Cylindrosporium, but perhaps
might be referred to Cercoseptoria Petrak.
Cercospora sequoias var. juniperi Ell. & Ev., so-called, was
destructive to plantings of Juniperus communis var. depressa
in the University of Wisconsin Arboretum. Professor Chupp
doubts that this is a good Cercospora, and states that in any
case it bears so little resemblance to C. sequoiae it can hardly be
considered a variety thereof.
So far as I am aware the only hitherto known station for
Cercospora fusimaculans Atk. on Leptoloma cognatum is Mad¬
ison where I collected it in 1942. It has been found recently on a
Greene — Notes on Wisconsin Parasitic Fungi . VI. 258
specimen of the same host from Muscoda, Grant Co., collected in
1935, but filed away at the time and later overlooked.
The rare Cercospora sanguinariae Peck was found in abun¬
dance on Sanguinaria canadensis in Baxter's Hollow, Town of
Sumpter, Sauk Co., July 10, and also at Ridgeway, Iowa Co.,
July 24. As Peck states “Owing to the scattered mode of growth
of the flocci the fungus is scarcely visible, but the large smoky-
brown spots are very conspicuous.” One scanty earlier collection
of this was made at Phlox, Langlade Co., in 1914.
Cercospora lythri (West.) Niessl developed quite generally
on Lythrum alatum at Madison. This is an exceedingly incon¬
spicuous fungus, but its presence is detectable by the pronounced
reddening of the host leaves. This species is perhaps more com¬
mon than would be indicated by the two collections in the her¬
barium. (Davis took a specimen at Racine in August 1900).
Additional Hosts
The fungi mentioned in the following list have been previous¬
ly reported as occurring in Wisconsin, but not on the particular
hosts cited here.
Albugo Candida (Pers.) 0. Ktze. on Lepidium campestre.
June 7. The weedy host has become widespread in southern
Wisconsin.
Premia lactucae Regel on Lactuca ludoviciana. August 29.
Microsphaera alni (Walk*.) Wint. on Betula sandbergii.
September 10.
Erysiphe polygoni DC. on Delphinium cidtorum. October
12. University Horticultural Gardens.
Erysiphe cichoracearum DC. on Galium aparine. July 7.
In this material the perithecia are very large, approaching the
upper size limits for the species. Davis (Trans. Wis. Acad. Sci.
18(1) : 252, 1915) mentions that at one time at Racine there
occurred a destructive outbreak of Erysiphe on this host. He
states “On examination from time to time no spores were found
in the asci and no specimens were preserved for that reason
as I did not know at that time that they were not formed during
the season. . . .” However that may be, in the present material
the characteristic spores and asci are well developed. A massive
growth of the host was completely covered by the mildew, peri¬
thecia being developed even on the fruits.
254 Wisconsin Academy of Sciences, Arts and Letters
The fungus known as Sphaeria solidaginis Schw. (of ques¬
tionable status) listed by Davis as occurring on Solidago altis-
sima in Wisconsin is also found on Solidago serotina. October
12, 1942.
Hypomyces lactifluorum (Schw.) Tul. on Cantharellus sp.
July 18. This seems not to have been reported before on Can¬
tharellus in these lists, although it is not rare. Specific identifi¬
cation of the host cannot be made because of the distortion
caused by the systemic infection.
Eocrqnartium muscicola (Pers. ex Fr.) Fitzp. on Homo-
mallium adnatum ( Amblystegiella adnata). Sauk Co., Parfrey’s
Glen, July 10. Coll. Prof. G. S. Bryan. Host det. by Prof. R. I.
Evans.
COLEOSPORIU M TEREBINTHINACEAE (Schw.) Arth. II, III on
Silphium terebinthinaceum. On seedling leaves. October 6. Da¬
vis collected this on Silphium perfoliatum at Lancaster, Grant
Co., suggesting that the fungus was probably not a permanent
member of the Wisconsin flora. The present collection, however,
seems to offer evidence for the affirmative.
Uropyxis amorphae (Curt.) Schroet. I on Amorpha fruti -
cosa. Sauk Co., Town of Prairie du Sac. Two collections made
by Davis in 1931 and 1932 bear the uredinoid aecia, clustered
and in close association with the pycnia. Uredia and telia only
have hitherto been reported for Wisconsin. Davis undoubtedly
saw the pycnia, but holding to the older usage, regarded the
associated structures as uredia rather than aecia. The change is
made to conform with Arthur's manual of the rusts, the accepted
standard of present-day workers in this region. Determination
confirmed by Dr. Cummins.
PUCCINIA GRAMJNIS Pers. Ill on Koeleria cristata. Bayfield
Co., Iron River, September 16, 1937. Coll. N. C. Fassett (No.
19119) This appears to be an eastward extension of the range
insofar as this host is concerned. Determination confirmed by
Dr. Cummins.
Puccinia extensicola Plowr. I on Aster paniculatus var.
simplex ( Aster tradescanti) , June 14.
Puccinia helianthi Schw. I on Helianthus grosseserratus .
June 18. ; on Helianthus giganteus , June 19.
Gymnosporangium globosum Farl. I on Crataegus mollis.
Greene — Notes on Wisconsin Parasitic Fungi. VI. 255
September 6; on Crataegus monogyna ( C . oxyacantha). Sep¬
tember 15. Seemingly rarely developed on the latter host.
Phyllosticta trillii Ell. & Ev. on Trillium declinatum.
Dane Co., Mt. Vernon, July 5, 1938. This is referred here with
doubt. Davis reported this on Trillium cernuum and I have
listed it on T. grandiflorum. Careful microscopic comparison of
ail three collections indicates that this fungus might perhaps
better be assigned to Gloeosporium, although it is surely not
Gl. trilli Ell. & Ev. On the other hand, the leaves of Trillium
are very thin, which might account for the imperfect develop¬
ment of the pycnidia.
Phyllosticta minutissima Ell. & Ev. on Acer/rubrum.
September 14. Probably merely the precursor of a perfect stage
with the tiny “conidia” non-germinable.
Phyllosticta desmodii Ell. & Ev. on Desmodium canadense.
August 19.
Phyllosticta liatridis J. J. Davis on Liatris spheroidea
f. benkei. Waukesha Co., Eagleville, August 8. The lesions here
are very similar to those of the type specimen on Liatris spicata ,
but the spores are somewhat smaller and verging on the ellip¬
soidal.
Phyllosticta labruscae Thiim. on Parthenocissus tricuspi-
data (cult.). July 25.
Phyllosticta nebulosa Sacc. on Silene latifolia. July 8; on
Silene dichotoma. July 13.
Ascochyta pisi Lib. on leaves of Lupinus perennis. June 7.
The spores here are of about the size specified by Sprague (Phy¬
topath. 19: 927, 1929) for this fungus as it appears on Pisum
sativum and varieties, i. e., usually rather narrow and with the
mean spore length less than 13.5^.
Stagonospora atriplicis (West.) Lind, on Atriplex patula
var. littoralis. Dane Co., Black Earth, August 11, 1941. Coll.
M. P. Backus.
Stagonospora apocyni (Peck) Davis on Apocynum canna-
binum. August 5. This was excellent material and developed in
quantity. Judging by his remarks, Davis seems at one time to
have had an unsatisfactory specimen on A. cannabinum, but
there is no collection of his in the herbarium.
Septoria populi Desm. occurred as a disfiguring and defoli-
256 Wisconsin Academy of Sciences , Arts and Letters
ating leaf blight on a large array of poplar hybrids in a nursery
in the University Arboretum. The infection was so severe as
bring into serious question the desirability of these trees as
subjects for ornatmental plantings. Some of the hybrids affected
were as follows (the names are those employed by the nursery¬
men and are certainly in some cases botanically incorrect.) :
Populus berolinensis X angidata, P. charkowiensis X caudina ,
P. charkowiensis X trichocarpa, P. maximowiczii X berolinen¬
sis, P. maximowiczii X plantierensis, P. maximowiczii X tricho¬
carpa, P. nigra X laurifolia , P. nigra X trichocarpa, P. nigra
betulifolia X trichocarpa, P. petrowskyana X caudina, P. raswr
moskyana X caudina, P. sargentii X berolinensis rossica, and
P. tacamahacca candicans X berolinensis.
Septoria violae West, on Viola sagittata . July 4. The spor-
ules are small, 16-20 X 1/*, the dimensions given by Diedicke in
the Kryptogamenflora der Mark Brandenburg.
Septoria polygonorum Desm. on Polygonum persicarwL
July 29. Also found on a phanerogamic specimen of this host
collected by Prof. N. C. Fassett at St. Croix Falls, Polk Co., Sep¬
tember 3, 1927.
Septoria melandrii Pass, on Lychnis flos-cuculi . Sheboygan
Co., Sheboygan, June 1903. On a phanerogamic specimen col¬
lected by the late Chas. Goessl; on Silene dichotoma, Madison,
July 13. Although this species seems not to have been reported
on Silene, it corresponds well with S. melandrii as it appears on
Lychnis alba. The sporules are up to 65/x long.
Septoria Scutellariae Thum. on Scutellaria parvula var.
ambigua. June 17. This seems not to have been reported before
on this host from Wisconsin or elsewhere.
Septoria lysimachiae West, on Lysimachia terrestris. Au¬
gust 24. Apparently the first report of Septoria on this host.
Septoria sonchifolia Cke. on Sonchus arvensis. July 13.
Also found on a phanerogamic specimen of the same host col¬
lected at Appleton, Outagamie Co., in 1928.
Leptothyrium punctiforme B. & C. on Erigeron ramosm .
June 9.
Marsonia fraxini Ell. & Davis on Fraxinus americana. Au¬
gust 5. The large uniseptate conidia are here borne in definite
acervuli. Typical conidia measure 35-40 X 5-6^.
Greene — Notes on Wisconsin Parasitic Fungi . VI. 257
Colletotrichum solitarium Ell. & Barth, on Solidago jun-
cea. August 16.
Cylindrosporium betulae J. J. Davis on Betula sandbergii.
July 30. Most of the specimens in the herbarium appear to be
on the hybrid rather than on B . pumila as labelled.
Cylindrosporium artemisiae Dearn & Barth, on Artemisia
ludoviciana. June 12.
Ramularia virgaureae Thtim. on Aster ptarmicoides. Sep¬
tember 1. Many of the conidia in this specimen are of the Cerco-
sporella type, up to 100/x long. It is possible that a scanty earlier
collection on A . ptarmicoides from Eagleville, Waukesha Co.,
which was referred to Ramularia asteris (Phil. & Plowr.)
Bubak, should have been placed under R. virgaureae.
Ramularia taraxaci Karst, on Taraxacum erythrospermum.
May 26.
Scolecotrichum GR A MINIS Fckl. on Muhlenbergia racemosa.
August 24.
Helminthosporium sativum Pamm., King & Bakke on Ag-
ropyron repens. May 24. Professor J. L. Allison of the Depart¬
ment of Plant Pathology at the University of Wisconsin informs
me that he has collected PI. sativum on quack grass on several
occasions.
Cercosporella cana Sacc. on Erigeron philadelpkicus.
July 4.
Cercospora muhlenbergiae Atk. on Muhlenbergia race¬
mosa . August 14.
Cercospora polygonacea Ell. & Ev. on Polygonum convolvu¬
lus . July 1. Determination confirmed by Prof. Chupp.
Cercospora violae Sacc. on Viola sagittata. July 4. Deter¬
mined by Prof. Chupp.
Cercospora parvimaculans J. J. Davis on Solidago altissi-
ma. August 24.
Cercospora bidentis Tharp on Bidens coronata. September
10. The first report of Cercospora on this host. Determination
confirmed by Prof. Chupp.
Additional Species
The species listed below have not previously been reported
to occur in Wisconsin.
258 Wisconsin Academy of Sciences, Arts and Letters
Synchytrium holwayi Farl. on Monarda fistulosa. A small
collection made on June 29, but found in abundance in the same
vicinity July 27. This species has resting sporangia much small¬
er than those of Synchytrium aureum.
According to Professor Mix (Mycologia 30: 570-5, 1938) the
report of Taphrina filicina Rostr. on Cystopteris fragilis in
Wisconsin is erroneous and the fungus should be referred to
Taphrina cystopteridis Mix n. sp.
Sclerotina laxa Aderh. & Ruhl. (Monilia stage) has been
found on sour cherry ( Prunus cerasus) in Door Co. Coil. J. D.
Moore, June 1, 1942. Det. G. W. Keitt.
Naemacyclus niveus (Pers. ex Fr.) Sacc. on Finns sylves-
iris (cult.). May 1. On fallen needles. Det. Dr. G. D. Darker.
Clements and Shear place this interesting fungus in the family
Stictidaceae of the Phacidiales. It is differentiated from similar
forms in the Hysteriaceae by color and consistency and by the
disk being widely exposed at maturity. This organism causes
a typical needle casting of pines, and Darker in his “Hypoder-
mataceae of Conifers” states that the disease is of sufficient im¬
portance to warrant careful investigation.
Doassansia occulta (Hoffm.) Cornu on Potamogeton
gramineus var. graminifolius. Douglas Co., Town of Lake Ne-
bagamon, Sect. 1, T46N, R11W, August 22. Coll. N. C. Fassett.
Host det. by Prof. Fassett.
Puccinia virgata Ell. & Ev. II, III on Sorghastrum nutans.
October 2. Profuse development of uredia was observed as early
as the last week in August.
Phyllosticta hispida Ell. & Dearn. on Smilax hispida.
Dane Co., near Sauk City, October 15, 1935. Coll. Davis &
Greene. The conidia are very small, of the bacillary type, 5-6 X
1/a. The material was overwintered but failed to develop further.
This is plainly the same thing which was issued under this name
as No. 3541 in North American Fungi.
Phyllosticta violae Desm. on Viola sp. (probably V. pube-
scens). July 19. In this specimen the conidia are about 10-13
X 3.5-4.5/a. Davis in his “Parasitic Fungi of Wisconsin”, p. 67,
states “Phyllosticta violae Desm. was included in the Provi¬
sional List, but I find no Wisconsin specimen.” The species is
therefore entered here as new to the state.
Greene — Notes on Wisconsin Parasitic Fungi. VI. 259
Phyllosticta rosae Desm. on Rosa sp. September 2. Prob¬
ably not uncommon, but apparently hitherto unreported.
Phyllosticta monardae Ell. & Barth, on Monarda fistulosa.
August 19. Referred here with some doubt. The spots are con¬
spicuous, with a small rounded light gray center, about 1 mm.
diam., and a wide much darker border, the whole producing a
suborbicular spot 3-5 mm. diam. The spores are of the dimen¬
sions specified in the original description. A Phyllostica found
on Blephilia ciliata , June 25, is likewise assigned to Ph. mon¬
ardae. The conidia are small 4-6 X 1-5/*, and the pycnidia, which
are about 100/* diam., are borne on very small, arid, purple-
bordered spots. The spots are of the type so frequently seen on
Monarda fistulosa which have been, in my experience, consistent¬
ly sterile.
Phyllosticta siccata n. sp.
Spots white, arid, suborbicular, sunken, with raised border,
1-2 mm. diam.; pycnidia epiphyllous, gregarious, subglobose,
olivaceous, thin-walled, ostiolate, 75-125/* diam.; conidia hya¬
line, ellipsoid, 4-5 X 3-3.5/*.
On leaves of Solidago serotina. Madison, Wis., U. S. A., July
14, 1943.
Phyllosticta siccata sp. nov.
Maculis albidis, aridis, suborbicularibus, depressis, cum mar-
ginibus elevatis, 1-2 mm. diam. ; pycnidiis epiphyllis, gregariis,
subglobosis, olivaceis, muris tenuibus, ostiolatis, 75-125/* diam.;
conidiis hyalinis, ellipticis, 4-5 X 3-3.5/*.
In foliis Solidaginis serotinae. Madison, Wis., U. S. A.
Sclerophoma pithyophila (Cda.) v. Hoehn. occurs com¬
monly on fallen needles of various pines (e. g., Pinus banksiana ,
P. resinosa, P. strobus and P. sylvestris in Wisconsin). While
this fungus is probably normally a saprophyte it appears that it
may occasionally function as a weak parasite. Many small trees
of Pinus strobus in a plantation in the University Arboretum
show foliage with the individual needles brown and dead to
about halfway back from the tip, but still green at the base.
The brown portions are thickly beset with the erumpent pyc¬
nidia of S. pithyophila. It is possible that insects are primarily
responsible for the discoloration, but not impossible that the
fungus may also be involved. In addition to the above-mentioned
pines, a scanty collection was made on languishing foliage of
260 Wisconsin Academy of Sciences, Arts and Letters
P. yonder osa (cult.), and it is of interest that a fungus which is
morphologically identical with S. pithyophila occurred on dead
twigs of Larix laricina.
Selenophoma DONACis (Pass.) Sprague & Johnson on Pani-
cum virgatum . Columbia Co., Lodi, June 30, 1938; Dane Co.,
Madison, August 1942 and 1943. This is what was formerly
called Septoria donacis Pass. f. panici Ell. & Barth. In a per¬
sonal communication Dr. Sprague states “These things have no
business being in Septoria. They have falcate spores, are non-
septate, have characteristically smallish globular pycnidia with
coarse polygonal cell structure, stout cuspidate pycnophores, and
produce a characteristic scurfy growth on media.” According
to Dr. Sprague this species is common in the prairie country,
but there seem to be no previous reports for Wisconsin.
Septoria mitellae Ell. & Ev. on Mitella diyhylla. On green,
overwintered leaves (basal). Vernon Co., Westby, May 9.
Septoria wisconsina n. sp.
Spots none ; tips of leaflets pale brown ; pycnidia almost con-
colorous, gregarious, deeply imbedded, amphigenous, globose,
small 50-75/a diam. ; ostioles wide, thickened rings of tissue,
prominent, 20-30/a diam. ; conidia acicular, slightly curved, con¬
tinuous or more or less distinctly septate, 12-25 X 1 .5/a.
On leaves of Astragalus canadensis. Madison, Dane Co.,
Wis., U. S. A., July 28, 1943.
Septoria wisconsina sp. nov.
Maculis nullis, foliis pallidis brunneis apici, pycnidiis prope
concoloribus, gregariis, immersis, amphigenis, globosis, parvis,
50-75/a diam.; ostiolis latis, crassis annulis, prominentibus,
20-30/a diam.; conidiis acicularibus, leviter curvatis, continuis
vel plusve minusve distincte septatis, 12-25 X 1.5/a.
In foliis Astragali canadensis. Madison, Wis., U. S. A.
This is different from other species described on Astragalus,
none of which have conidia as short and slender as those of
S. wisconsina.
Septoria eupatorii Rob. & Desm. on Euyatorium yerfolia-
tum. July 20. There seems to be no previous record of this fun¬
gus on E. yerfoliatum.
Dr. Berch Henry of the Department of Plant Pathology at
the University of Wisconsin has given to the herbarium a speci¬
men of needles of Pinus nigra var. Obustriaca bearing a parasite
Greene — Notes on Wisconsin Parasitic Fungi . VI. 261
that he identifies as Lecanosticta acicola (Thiim.) Syd. (Sep-
toria acicola (Thum.) Sacc.). This was the cause of so-called
brown spot disease of Austrian pine in a nursery at Waterloo,
Jefferson Co., June 1943. Wolf and Barbour (Phytopath. 31:
61-74, 1941) have published on this disease.
Protocoronospora nigricans Atk. & Edg. on Vicia villosa.
September 4.
Gloeosporium leptothyroides Kab. & Bub. on Betula sand-
bergii. July 30. This corresponds well with the description and
with No. 429 of the Fungi imperfecti exsiccati issued by Kabat
and Bubak.
Helminthosporium leucostylum Drechsler on Eleusine in -
dica. August 14. Dr. C. L. Lefebvre suggests that this is very
similar to Helminthosporium hadrotrichoides Ell. & Ev. on
Eragrostis cilianensis.
Helminthosporium inconspicuum C. & E. var. buchloes
Ell. & Ev. was found in July on Buchloe dactyloides (cult.),
Bouteloua hirsuta , and Bouteloua curtipendula. The specimen on
Buchloe was collected by Prof. J. L. Allison. Dr. Sprague in¬
forms me that this is common on buffalo grass on the great
plains, and also occurs on grama grass.
Helminthosporium leucostylum Drechsler on Eleusine in -
lianensis . September 16. Determined by Dr. Lefebvre.
A rather perplexing fungus has been found on leaves of
Cer ostium vulgatum. This is a very delicate form, being scarcely
discernible with a good hand lens. It is close to Cercospora, so
material was submitted to Professor Chupp. He considers that
because of the extremely slender non-tapering conidia it is not a
good Cercospora. The conidiophores are rudimentary and very
short. Petrak (Ann. Myc. 23: 68-70, 1925) sets out the new
genus Cercoseptoria from the Cercospora-Cercosporella com¬
plex, and the fungus in question seems to fall under that genus
as defined. No similar form appears to have been described on
Cerastium or related genera, so the fungus is described as Cer¬
coseptoria CERASTII n. sp.
Cercoseptoria cerastii n. sp.
Spots none; fruiting amphigenous, mostly hypophyllous ; tu¬
bercles intrastomatal, brown, 35-40^ diam. ; conidiophores nar-
raw, very short, almost obsolete, 5-10 ^ long; conidia hyaline,
slender, filiform, continuous, slightly curved, 35-70 X 1/*.
262 Wisconsin Academy of Sciences, Arts and Letters
On leaves of Cerastium vulgatum. Madison, Wis., U. S. A.,
July 1, 1943.
Cercoseptoria cerastii sp. nov.
Maculis nullis; fructificationibus amphigenis, plerumque hy-
pophyllis ; tuberculis in stomatis, brunneis, 35-40/x diam. ; conid-
iophoris angustis, brevissimis, prope obsoletis, 5-10^ longis;
conidiis hyalinis, angustis, filiformibus, continuis, leviter curva-
tis, 35-70 X 1/*.
In foliis Cerastii vulgati. Madison, Wis., U. S. A.
Cercosporella ontariensis Sacc. on Euthamia graminifo-
lia. June 25. This has been compared with Fungi Columbiani
No. 4710, issued as C. ontariensis, and seems to be the same
thing. For convenience’ sake I have thus listed the Wisconsin
specimen, although to me it seems doubtful that it is a species
distinct from the inter-grading assemblage of Ovularia-Ramu-
laria-Cercosporella-like fungi that occur on various solidagini-
colous hosts. Davis would perhaps have referred this to Ramu-
LARIA VIRGAUREAE Thlim.
Cercospora SEMINALIS Ell. & Ev. on Buchloe dactyloides
(cult.). Coll. & det. by Prof. J. L. Allison. It seems probable
that the parasite was imported with the host.
Cercospora cannabis (Hara) Chupp n. comb. (Syn. Cerco-
sporina cannabis Hara). On Cannabis sativa Professor Chupp
states that the only other specimen of this species reported from
the United States was sent to him from Missouri. Madison,
August 13.
Cercospora acetosellae Ell. on Rumex acetosella. August
20. Determination confirmed by Professor Chupp.
Cercospora thlaspiae Chupp & Greene n. sp.
On silicles, spots minute to large, dark olivaceous to almost
black, covered with minute black pustules ; stromata small, dark
olivaceous brown ; fascicles 2-12 spreading stalks ; conidiophores
pale to medium in color and width, tips narrow and paler, in¬
distinctly multiseptate, straight to mildly curved, not branched,
rarely geniculate, subtruncate tip, 4-5.5 X 50-400/x ; conidia hy¬
aline, acicular, straight to curved, indistinctly multiseptate, base
truncate, tipe acute to subacute, 2-4 X 40-300 fx.
On silicles of Thlaspi arvense. Dane Co., near Sauk City,
Wis., U. S. A., July 10, 1943.
Greene — Notes on Wisconsin Parasitic Fungi . VL 263
Cercospora thlaspiae sp. nov.
In fructibus, maculis minutis vel magnis, fuscis-olivaceis vel
prope nigris, cum nigris pustlis minutis ; stromatis parvis, fuscis
olivaceo- brunneis; fasciis 2-12 cauliculis divergentibus ; conid-
iophoris pallidis vel mediis brunneis, latitudinibus mediis, apici-
bus pallidis, angustioribus, indistincte multiseptatis, rectis vel
leviter curvatis, non ramosis, raro geniculatis, apicibus sub-
truncatis, 4-5.5 X 50-400/x ; conidiis hyalinis, acicularibus, rectis
vel curvatis, indistincte multiseptatis, basibus truncatis, apicibus
acutis vel subacutis, 2-4 X 40-300/a.
In fructibus Thlaspi arvensis. Dane Co., Wis., U. S. A.
Cercospora uramensis Chupp & Muller on Cleome spinosa
(cult.). University of Wisconsin campus, August 30. Professor
Chupp states that he had previously seen this only on Cleome sp.
from the type locality in Venezuela. Some of the conidia in the
Madison specimen are considerably longer than the upper limit
of 125/a set forth in the description. (Bol. Soc. Venez. Cien. Nat.
8 (52) : 58, 1942).
Cercospora potentillae Chupp & Greene n. sp.
Spots subcircular, 0.5-3 mm. diam., brown center, wide dark
red border ; fruiting chiefly epiphyllous ; stromata mostly a few
large brown cells ; fascicles 2-10 diverging stalks ; conidiophores
pale olivaceous brown, fairly uniform in color, somewhat irreg¬
ular in width, multiseptate, not branched, not or only once gen¬
iculate, slightly curved or bent, subtruncate tip, 4-5.5 X 40-
170/a; conidia hyaline, acicular, straight to curved, indistinctly
multiseptate, base truncate, tip acute, 2-4 X 40-160/a.
On leaves of Potentilla recta. Madison, Wis., U. S. A., July 7,
1943.
Cercospora potentillae sp. nov.
Maculis subrotundatis, 0.5-3 mm. diam., centris brunneis,
marginibus latis, fuscis rubris ; f ructificationibus plerumque epi-
phyllis; stromatibus paucis magnis cellis brunneis; fasciis 2-10
cauliculis divergentibus; conidiophoris pallidis olivaceis brun¬
neis, coloribus plerumque uniformibus, latitudinibus nonnihil
irregularibus ; multiseptatis, non ramosis, non vel 1-geniculatis,
leviter curvatis vel sinuosis, apicibus subtruncatis, 4-5.5 X 40-
170/a; conidiis hyalinis, acicularibus, rectis vel curvatis, indis¬
tincte multiseptatis, basibus truncatis, apicibus acutis, 2-4 X
40-160/a.
264 Wisconsin Academy of Sciences, Arts and Letters
In foliis Potentillae rectae. Madison, Wis., U.S.A.
Cercospora potentillae has also been found on Potentilla
norvegica var. hirsuta at Madison, August 1943.
Cercospora astragali Woronichin on Astragalus canaden^
sis . July 20. Determined by Professor Chupp who states that
he believes this is the first report of this species other than the
type.
Cercospora desmodiicola Atk. on Desmodium canadense.
September 8. Determined by Professor Chupp.
In my third series of notes there was mention of a species
of Cercospora on Oxalis stricta which Professor Chupp identi¬
fied as C. oxalidiphila Speg. ined. A description of this by
Chupp & Muller has appeared (Bol. Soc. Venez. Cien. Nat. 8
(52) : 52, 1942) so the species is here included among fungi new
to the state.
Cercospora grisea Cke. & Ell. on Polygala sanguinea . Sep¬
tember 7.
Cercospora vulpinae Ell. & Kell, on Vitis mdyina. August
16. Determined by Professor Chupp who finds the specimen to
be not quite mature.
Cercospora lecheae Chupp & Greene n. sp.
Spots minute, reddish, turning yellowish to pale or brown¬
ish; fruiting chiefly hypophyllous, stromata a few brown cells
filling the stomatal opening; fascicles 2-12 spreading stalks;
conidiophores pale to medium brown, fairly uniform in color and
width, indistinctly 0-3 septate, rarely branched, slightly curved,
undulate or tortuous, not geniculate, conic tip, 3-5.5 X 15-80/a;
conidia very pale olivaceous, obclavate, shortest ones cylindric,
straight to mildly curved, indistinctly 1-5 septate, base obconi-
cally truncate, tip subobtuse, 2.5-5 X 15-70/a.
On leaves of Lechea intermedia. Madison, Wis., U. S. A.,
September 8, 1943.
Cercospora lecheae sp. nov.
Maculis minutis, rufulis, mutantibus ochraceis vel brunneo-
lis ; f ructificationibus plerumque hypophyllis ; stromatibus paucis
brunneis cellis, replentibus stomatis; fasciis 2-12 cauliculis di-
vergentibus; conidiophoris pallidis mediisve brunneis, coloribus
et latitudinibus prope uniformibus, indistincte 0-3 septatis, rare
ramosis, leviter curvatis, undulatis vel tortis, non geniculatis,
Greene — Notes on Wisconsin Parasitic Fungi . VI. 265
apicibus conicis, 3-5.5 X 15-80/*; conidiis pallidissimis olivaceis,
obclavatis vel cylindraceis si brevissimis ; rectis vel leviter curva-
tis, indistincte 1-5 septatis, basibus obconicis truncatis, sub-
©btusatis, 2.5-5 X 15-70/*.
In foliis Lecheae intermediae . Madison, Wis., U. S. A.
The two other species on the Cistaceae, C. helianthemi and
€. CISTINEARUM, have hyaline conidia.
Cercospora apii Fres. on Avium graveolens (cult.) August
26, 1941. Coll. R. E. Vaughn. This species seems not to have
been reported before in these notes, nor is there any other speci¬
men from Wisconsin in the herbarium.
There is in the Davis Herbarium at the University of Wis¬
consin a specimen on Zizia cor data from which, presumably,
Ellis and Everhart described Cylindrosporium ziziae. I had
occasion to examine this and failed to find any Cylindrosporium,
but did find a well-marked Cercospora. This was submitted to
Professor Chupp in the belief that it might be Cercospora
platyspora Ell. & Holw. However, he finds it to be a new species,
and it is therefore described as Cercospora cordatae Chupp &
Greene. (It would seem that the name Cylindrosporium ziziae
is highly dubious at best and should in all probability be dropped.
No. 429 of the Fungi Dakotenses, issued as Cylindrosporium
ziziae, appears (so far as the specimen at Wisconsin is concerned
at any rate) to be good Cercospora ziziae Ell. & Ev. which is
even farther removed from Cylindrosporium.)
Cercospora cordatae n. sp.
Spots angular to elongate, 1-2 X 2-5 mm., brown; fruiting
chiefly hypophyllous ; stromata a few hyaline to brown cells be¬
low stomatal openings ; fascicles dense, compact, filling stomata!
opening; conidiophores subhyaline to pale brown, tip frequently
hyaline, irregular in width, not or rarely septate, not branched,
rarely geniculate, bluntly rounded tip with large spore scar,
sometimes several spore scars near tip, 4-7 X 10-35/*; conidia
hyaline, cylindric, 0-3 septate, base subtruncate, tip obtuse, 4-6
X 15-65/*, straight to mildly curved.
On leaves of Zizia cordata. Coll. J. J. Davis, Racine, Wis.
U. S. A., June 22, 1890.
Cercospora cordatae sp. nov.
Maculis angulosis vel elongatis, 1-2 X 2-5 mm., brunneis;
froctificationibus maxime hypophyllis ; stromatibus paucis cellis
266 Wisconsin Academy of Sciences , Arts and Letters
hyalinis vel brunneis infra stomatis; fasciis densis, solidis, re-
plentibus stomatis; conidiophoris subhyalinis vel brunneis palli-
dis, apicibus frequenter hyalinis, latitudinibus irregularibus,
plerumque non-septatis, non ramosis, raro geniculatis, apicibus
obtusatis, rotundatis, cum sporis cicatricibus magnis, interdum
paucis cicatricibus ad apices, 4-7 X 10-35/*; conidiis hyalinis,
cylindraceis, 0-3 septatis, basibus subtruncatis, apicibus obtusa¬
tis, 4-6 X 15-65/*, rectis vel leviter curvatis.
In foliis Ziziae cordatae. Racine, Wis., U. S. A.
Cercospora elaeochroma Sacc. on Asclepias amplexicatdis .
July 18. Determined by Professor Chupp.
Cercospora verbenicola Ell. & Ev. on Verbena stricta. Au¬
gust 16. Professor Chupp informs me that Cercospora ver-
benae-strictae Peck is a synonym for C. verbenicola. There
are several earlier specimens in the herbarium, listed as C. VER-
benae-strictae.
Cercospora blephiliae Chupp & Greene n. sp.
Spots subcircular, 2-6 mm. diam., brown or rarely with al¬
most gray center ; fruiting chiefly epiphyllous ; stromata none or
a few brown cells ; fascicles 2-15 spreading stalks ; conidio-
phores pale to medium olivaceous brown, almost hyaline apex,
uniform in width, multiseptate, not branched, 0-2 geniculate,
tip subtruncate, 4-5 X 30-150/*; conidia hyaline, acicular, occa¬
sionally cylindric when short, indistinctly multiseptate, straight
to mildly curved, base truncate, tip subacute, 2-4.5 X 30-200/*.
On leaves of Blephilia ciliata. Scuppernong Prairie, 2 miles
northwest of Eagle, Waukesha Co., Wis., U. S. A., August 8,
1943.
Cercospora blephiliae sp. nov.
Maculis subrotundatis, 2-6 mm. diam., brunneis vel raro cum
centris prope griseis; fructificationibus plerumque epiphyllis;
stromatibus nullis vel paucis brunneis cellis; fasciis 2-15 cauli-
culis divergentibus ; conidiophoris palladis vel mediis olivaceo-
brunneis, apicibus prope hyalinis, latitudinibus uniformibus,
multiseptatis, non ramosis, 0-2 geniculatis, apicibus subtrunca¬
tis, 4-5 X 30-150/*; conidiis hyalinis, acicularibus, nonnumquam
cylindraceis si brevis, indistincte multiseptatis, rectis vel leviter
curvatis basibus truncatis, apicibus subacutis, 2-4.5 X 30-200/*.
In foliis Blephiliae ciliatae . Eagle, Waukesha Co., Wis.,
U. S. A.
Greene — Notes on Wisconsin Parasitic Fungi . VI. 267
Cercospora lobeliae Ell. & Ev. on Lobelia spicata . Au¬
gust 16.
Cercospora solidaginis Chupp & Greene n. sp.
Spots none, fruiting effuse, olivaceous, in numerous minute
patches 0.5-2 mm. diam., stromata lacking; nonfasciculate to
dense compact fascicles; conidiophores medium to dark brown,
uniform in color, somewhat irregular in width, 0-7 septate, when
nonfasciculate arising as branches from procumbent threads,
rarely geniculate, variously curved or bent, tip conic to blunt,
3-5.5 X 10-50/*; conidia pale or very pale olivaceous, longest
ones obclavate-cylindric, shorter ones distinctly cylindric,
straight or mildly curved, ends rounded bluntly or base short
obconically truncate, 1-7 septate, 2.5-5 X 15-50/a.
On leaves of Soliclago juncea. Madison, Wis., U. S. A., Au¬
gust 18, 1943.
Cercospora solidaginis sp. nov.
Maculis nullis; fructificationibus effusis, olivaceis, amphi-
genis, in numerosis minutis acervis, 0.5-2 mm. diam. ; stromati-
bus nullis; nonfasciculatis vel fasciculatis, fasciis nonnumquam
densis; conidiophoris mediis vel fuscis brunneis, coloribus uni-
formibus, latitudinibus nonnihil irregularibus, 0-7 septatis, si
nonfasciculatis ramis ab hyphis procumbentibus, raro genicu-
latis, varie curvatis vel sinuosis, apicibus conicis vel obtusatis,
3-5.5 X 10-50/a; conidiis pallidis vel pallidissimis olivaceis, si
longioribus obclavatis-cylndraceis, si brevioribus distincte cyl-
indraceis, rectis vel leviter curvatis, basibus obtusatis vel brevis
obconicis truncatis, 1-7 septatis, 2.5-5 X 15-50/a.
In foliis Solidaginis junceae. Madison, Wis., U. S. A.
Cercospora wisconsinensis Chupp & Greene n. sp.
Spots pale brown or whitish with narrow dark purple bor¬
der, rounded or angled, 1.5-5 mm. diam. ; fruiting amphigenous,
fascicles mostly not dense; conidiophores pale, tips paler and
narrower, not branched, undulate to geniculate above, medium
spore scar, tip subtruncate, 0-6 septate, variable, 3.5-5 X 15-
180/a, longest when hypophyllous ; conidia hyaline, acicular, 2-4
X 40-125/a ; longer conidia continuous or indistinctly septate;
shortest conidia narrow-obclavate, distinctly 4-5 septate.
On leaves of Prenanthes alba. Madison, Wis., U. S. A., Sep¬
tember 9, 1943.
268 Wisconsin Academy of Sciences, Arts and Letters
Ceecospora wisconsinensis sp. nov.
Maculis pallidis brunneis vel albentibus, marginibus angustis
fuscis purpureis, rotundatis vel angulosis, 1.5-5 mm. diam. ;
fructificationibus amphigenls; fasciis plerumque non densis ;
conidiophoris pallidis, apicibus pallidioribus et angustioribus,
non ramosis, supra undulatis vel geniculatis, sporis cicatricibus
mediis, apicibus subtruncatis, 0-6 septatis, variis, 3.5-5 X
15-180/x, si hypophyllis longissimis ; conidiis hyalinis, aciculari-
bus, 2-4 X 40-125^ ; conidiis longioribus continuis vel indistincte
septatis ; conidiis brevissimis angustis-obclavatis, distincte 4-5
septatis.
In foliis Prenanthis albae. Madison, Wis., U. S. A.
An earlier collection of this species was made at Eagleville,
Waukesha Co., August 31, 1941, but was held pending collection
of further confirmatory specimens. C. WISCONSINENSIS has also
been found in small quantity on Prenanthes racemosa at Madi¬
son, September 4, 1943.
Specimens of all new species described have been placed in
the University of Wisconsin Cryptogamic Herbarium. Those of
new species of Cercospora, described jointly with Professor
Chupp are also deposited in the herbarium of the Department of
Plant Pathology of Cornell University at Ithaca, New York.
SECOND GROWTH MAY SUPPLY TIMBER OF
EXCEPTIONAL QUALITY
Benson H. Paul
U. S. Forest Products Laboratory*
Investigations of wood reveal wide variations in quality due
to environmental conditions. Among hardwoods, second-growth
trees are likely to be more thrifty, the wood heavier, harder, and
stronger than in old-growth trees. Among softwoods, second-
growth trees, although more thrifty, usually supply wood that
is lighter, softer, and weaker than that of old-growth trees due
to the production of a higher proportion of springwood than
summerwood in the annual growth ring.
Although in the past much emphasis has been placed upon
locality of growth as influencing the quality of timber of a given
species, investigations of wood properties do not confirm impor¬
tant differences on that account except where a species may be
growing under extreme conditions of site. For example, jack
pine grown in the Nebraska sand hills under semi-arid condi¬
tions was inferior in strength because it was lacking in summer-
wood, the heavy dense portion of the annual growth ring. The
lack of summerwood may be attributed to a deficiency in soil
moisture during the growing season. Conversely, trees grown
under conditions of excessive moisture may produce wood of
unusual character for a species. A good illustration of this type
of behavior is ash grown in the Mississippi Delta where, be¬
cause of periodic flooding, the trees develop buttresses contain¬
ing light, weak wood. The wood from this source is far different
from upland ash and is unsuitable for customary uses of the
species.
So much for the extremes. A more common cause of varia¬
tion in the quality of wood is due to differences in environmental
conditions occurring among different stands in a locality, among
trees in a stand, or even at different periods in the life of a single
tree.
Maintained at Madison, Wisconsin, in cooperation with the University of Wisconsin.
269
270 Wisconsin Academy of Sciences, Arts and Letters
The individual tree responds to growth opportunities much
as a stalk of corn (although corn belongs to an entirely different
group of plants). In planting corn it is common practice to
check-row carefully in order to give each stalk sufficient space
to develop. In the natural forest all trees do not have equal
growing space. Through the many decades of the natural de¬
velopment of a forest stand, there exists a constant struggle first
for survival, later a continued competition among individual
trees for moisture, food, light, and air. In the virgin forest,
therefore, growth, even of dominant trees, is likely to be some¬
what restricted, especially during their later years.
In considering second-growth timber in comparison with old
growth, the trees comprising a second-growth stand frequently
compete less severely with each other than do trees of a virgin
forest. Many second-growth stands originate in such a way that
sharp competition does not take place during initial periods of
50 to 100 years. Often some of the trees are practically isolated
and are not obliged to compete with each other for growing
space. The result is that among broadleaved species, second-
growth stands may be expected to furnish heavier, harder,
stronger, and tougher wood than old-growth stands in the same
locality.
A familiar example of demand is for second-growth hickory
for handles, for wagon spokes in the old days, for auto wheels
in the early gasoline age, and more recently for many war uses
requiring wood of high shock-resisting ability. A scarcity of
hickory has led to attempts to use all classes of material, both
old-growth and second-growth, of the various hickory species.
Recently a number of hickory picker-sticks used in weaving were
submitted to the Forest Products Laboratory for an explanation
of the reasons for low strength of some, it being stated that both
good and poor hickory originated in the same locality. Tests of
the sticks showed wide differences in toughness. The narrow
growth rings and low density of the weak ones indicated that
they had been cut from slow-growing old trees, while the others
had the characteristic toughness and high density of second-
growth hickory. Such differences between old-growth and sec¬
ond-growth timber are more often recognized in species that are
relied upon for exacting uses. Hickory and ash are species used
when toughness and shock-resisting properties are required. In
Paul — Second Growth Timber
271
some other woods, hardness and wearing qualities are desired,
as, for example, in the use of dogwood for shuttles, hard maple
for floors, bearings, gears, or wood type.
A shortage of dogwood, the species formerly used almost ex¬
clusively for shuttles, has led to a search for substitutes. One of
the promising replacements appears to be second-growth sugar
maple of especially high density from thrifty open-grown trees.
Investigations of such open-grown sugar maple and com¬
parison with former tests of old-growth maple, and comparison
even with maple from typical second-growth woodlot stands,
show a marked increase in the weight and hardness of the open-
grown material. While results of earlier mechanical tests of
sugar maple and dogwood gave dogwood much higher values for
both these properties, recently the wood from the open-grown
sugar maple trees has been found practically equal to the aver¬
age weight and hardness of dogwood. Although such trees afford
only relatively short, usable log-lengths per tree, the number of
shuttles obtainable per tree may be much higher than from dog¬
wood because of the larger diameter attained by the sugar maple
trees.
Many other examples might be given of large differences be¬
tween old growth and second growth. Sometimes the second
growth manifests undesirable qualities; this is frequent in
second-growth coniferous species of rapid initial growth.
Research in wood that reveals the characteristics of all types
of growth helps in the selection of material best adapted to criti¬
cal wartime uses. In peacetime this knowledge will make it pos¬
sible, through appropriate silvicultural measures applied in the
forest, to grow timber having the special qualities that are most
desirable.
PRELIMINARY REPORTS ON THE FLORA OF
WISCONSIN. XXXI. BORAGINACEAE
Emil P. Kruschke
Milwaukee Public Museum
The following report is based on the study of herbarium
specimens and also on field observations made by the author.
The specimens on which this report is based are deposited in the
following herbaria: University of Wisconsin, Milwaukee Public
Museum, Field Museum, Marquette University, University of
Wisconsin in Milwaukee (Extension Division), Milwaukee State
Teachers College, Ripon College, Lawrence College, St. Norbert
College, and the private herbaria of Mr. S. C. Wadmond, Dela-
van, Wisconsin, Mr. Chas. Goessl, Sheboygan, Wisconsin, and my
own. The author gratefully acknowledges the loan of specimens
by Dr. N. C. Fassett, Mr. Chas. Goessl, Mr. Walter E. Rogers,
Mr. S. C. Wadmond, Dr. A. M. Keefe, and Dr. J. F. Groves. The
author is most appreciative for suggestions and information
given by Dr. N. C. Fassett and Dr. Lloyd Shinners of the Uni¬
versity of Wisconsin, and Mr. Albert M. Fuller of the Milwaukee
Public Museum, especially for their reading the manuscript, and
also to Mr. I. M. Johnston of the Gray Herbarium at Harvard
University for the verification and determination of a few speci¬
mens whose identifications were doubtful.
The family Boraginaceae was monographed in 1924 by Mr.
I. M. Johnston.1 This monograph has been of great help in the
study of this group of plants. Other scientific reports on sep¬
arate genera and species of this family have also been helpful in
this study. These articles are referred to in the text of this re¬
port.
The keys and text of this report are based primarily on the
author’s own observations. Separate flowering and fruiting keys
for the genera and for the species of Lithospermum are given so
as to make possible the identification of these plants in both the
flowering and fruiting stages.
1 1. M. Johnston : A synopsis of the American native and immigrant borages of the subfamily
Boraginoideae. Contr. Gray Herb. Harvard Univ. 70: 1-55- 1924.
273
274 Wisconsin Academy of Sciences, Arts and Letters
Flower Key to Genera
a. Corolla regular.
b. Style as long as the corolla or longer, conspicuous.
c. Throat of corolla closed by 5 scales . . 5. Symphytum
cc. Throat of corolla open or merely with crests or folds.
d. Corolla trumpet-shaped or tubular- campanulate, with shallow,
rounded, and spreading lobes. Flowers not in the axils of bracts;
flowers blue . 9. Mertensia
dd. Corolla tubular, with erect and acute sawtooth-like lobes. Flow¬
ers all in the axils of bracts; flowers yellow or whitish .
. 11. Onosmodium
bb. Style shorter than the corolla.
e. Flowers, at least the lowest ones, in the axils of bracts,
f. Throat of corolla closed by 5 scales.
g. Corolla 9-10 mm. long; calyx 5-7 mm. long; style
5.5-7.5 mm. in length; flowers deep blue or purplish-
blue . 7. Anchusa
gg. Corolla 2-4 mm. long; calyx very small, not over
3 mm. in length; style less than 3 mm. long; flowers
light blue or forget-me-not blue,
h. Inflorescence abundantly bracteate throughout;
leaves ribbon -like, less than 1 cm. wide .
. 2. Lappula
hh. Inflorescence sparsely bracteate at base or only
the lowest flowers in the axils of bracts: leaves
mostly more than 1 cm. wide . 3. Hackelia
ff. Throat of corolla open or merely with crests or folds.
i. Flowers all in the axils of bracts; plants hispid-
pubescent . 10. Lithospermum
ii. Only the lowest flowers in the axils of bracts;
rough herbs densely covered with white, bristly
hairs . 4. Amsinckia
ee. Flowers not in the axils of bracts.
j. Throat of corolla closed by 5 scales; lower stem-
leaves comparatively large, more than 8 cm. long;
venation of leaves fairly distinct. ...1. Cynoglossum
jj. Throat without scales, merely with transverse
crests; lower stem-leaves comparatively small, less
than 8 cm. long ; venation of leaves not distinct ....
. 8. Myositis
aa. Corolla irregular
k. Stamens and style included; throat of corolla closed by 5 scales;
stigma simple . 6. Lycopsis
kk. Stamens and style exserted; throat of corolla open; stigma 2-cleft
. 12. Echium
Fruit Key to Genera
a. Nutlets attached laterally to the receptacle,
b. Nutlets armed with barbed prickles.
Kmschke — Flora of Wisconsin . XX XL Boraginaceae 275
c. Nutlets inclined horizontally, armed all over with short, barbed
prickles; attached near the end ................... .1. Cynoglossum
cc. Nutlets erect or ascending, with barbed prickles on their backs or
margins; attached at least half their length along the median ven¬
tral keel.
d. Pedicels stout and not sharply bent downward in fruit; nutlets
equalling the subulate gynobase, attached nearly their full
length along the median ventral keel, lacking a well defined
areole; style usually surpassing the nutlets . . . .2. Lappula
dd. Pedicels slender, bent sharply downward in fruit; nutlets twice
surpassing the stout pyramidal gynobase, attached obliquely by
a deltoid or ovate areole; ventral keel extending over only the
upper half of the nutlet; style definitely surpassed by the nut¬
lets . . . . . . . . . 3. Hackelia
feb. Nutlets wrinkled or granular-roughened, not armed with barbed
prickles ................................................. 4. Amsinckia
. Nutlets attached to the receptacle at or very near the base.
e. Region of attachment of nutlet surrounded by an annular
rim, leaving a pit-like depression upon the flat or slightly
convex gynobase.
f. Nutlets nearly smooth; branch-veins of leaf conspicuous;
leaves large, 3-7.5 cm. wide . . 5. Symphytum
ff. Nutlets rough-wrinkled or rugose; branch-veins of leaf
inconspicuous, only the midrib evident; leaves less than
2.5 cm. wide.
g. Style conspicuously longer than the fruiting calyx;
margin of leaf unevenly undulate or sparsely and ir¬
regularly dentate .......................... 6. Lycopsis
.gg. Style about as long or only slightly longer than the
fruiting calyx, not conspicuous; margin of leaf entire
............ _ ..... _ ........... _ _ 7. Anchusa
ee. Region of attachment of nutlet not surrounded by an annular
rim and without a pit-like depression on the gynobase.
h. Style thread-like, long and conspicuous, persisting
in the fruiting stage (occasionally broken off in
mature fruits) .
i. Nutlets ivory-like, bony, white, smooth or only
slightly pitted . . . . . . 11. OnoBmodium
ii. Nutlets brown to brownish-gray, roughened,
wrinkled, or with blunt, irregular ridges.
j. Pedicels very short, not over 2 mm. long;
stigma 2-cleft; plants densely hispid -pubescent
throughout . . . ... 12. Echium
jj. Pedicels mostly 5 to 15 mm. long; stigma sim¬
ple; plants glabrous, or with inconspicuous
short hairs . 9. Meriensia
hh. No long, conspicuous, thread-like style present or
persisting in the fruiting stage; nutlets bony,
276 Wisconsin Academy of Sciences , Arts and Letters
smooth (rough-wrinkled to densely tubercled in
Lithospermum arvense, but nutlets definitely bony) .
k. Nutlets over 1 mm. in length, more or less
round in cross-section . .10. Lithospermum
kk. Nutlets less than 1 mm. in length and
laterally compressed . 8. Myosotis
1. CYNOGLOSSUM (Tourn.) L.
a. Calyx-lobes more than 3 mm. long; nutlets sunken in or depressed dor-
sally, with a definite elevated margin; stems leafy throughout,
b. Flowers reddish-purple or maroon, rarely white; nutlets 5-7 mm.
long . 1. C. officinale
bb. Flowers forget-me-not blue; nutlets small, not over 3 mm. in length
. . . .\ . 2. C. amabile
aa. Calyx-lobes less than 3 mm. long; nutlets convex dorsally and without
a definite elevated margin; upper part of stem leafless, terminating in a
once- or twice-forked, bractless inflorescence . 3. C. boreale
l. CYNOGLOSSUM officinale L. (Common Hound’s Tongue)
(Map 1). Frequent, especially in the southern and eastern
parts of the State. More extensive collecting in western and
northern Wisconsin would no doubt show it to be more common
than present collections indicate. The white-flowered form (C.
officinale L. f. bicolor (Willd.) Lehm.) is very rare. A specimen
of this form was collected by the author June 7, 1939, in Mil¬
waukee Co., T. of Oak Creek, on the Tischendorf farm, at the
border of a rich mesophytic woods. At this station there were
three specimens growing with the typical maroon-colored form.
Occurs chiefly in waste ground, pastures, along roadsides and
railroads, and in shrubby thickets and open woods. Flowering
from May 25 to July 15.
Native of Eurasia ; naturalized in North America.
2. CYNOGLOSSUM amabile Stapf & Drummond
(Map 2). The author collected several specimens of this
perennial in a Wauwatosa city dump, where it was growing as
an escape from garden cultivation. The plants were doing very
well and there were indications of its spreading. Flowering sea¬
son July and August. Native of S. W. China. Frequently culti¬
vated in gardens in this country.
3. CYNOGLOSSUM boreale Fern. (Northern Wild Comfrey)
(Map 2). This native American species is northern in its
range, occurring chiefly in the northern part of the State. How¬
ever, several collections have been made in the southern and
Kruschke — Flora of Wisconsin. XXXI. Boraginaceae 277
eastern parts. Dry woods and copses. Flowering from June 1
to July 15. Flowers pale blue.
2. LAPPULA (Rivin.) Moench
a. Fruits with a double row of stout, flattened prickles about the margin,
these prickles little or not at all confluent at the base ..... .1. L. echinata
aa. Fruits with a single row of stout, flattened prickles or bristles about the
margin, the prickles usually confluent at the base . . . . . . .
. . . . . . . 2. L. Redowskii var. occidentals
l. Lappula echinata Gilib. (Spiny or European Stickseed)
(Map 3). This species has been collected most frequently in
the southeastern part of the State, but the eastern and northern
parts are also fairly well represented in herbarium collections.
Apparently it is rare in the western part of the State. Usually
grows in dry, sandy-gravelly soil, in waste places, along road¬
sides, and in ballast along railroads. Flowering season June and
July. Flowers blue to bluish- white.
Native of Eurasia ; naturalized in North America.
2. Lappula redowskii (Hornem.) Greene, var. occidentalis
(Wats.) Rydb.
(Map 4). Represented by specimens collected from four sta¬
tions in the southwestern part of the State and a single speci¬
men collected in Sheboygan, the latter made by Chas. Goessl in
July, 1919. J. H. Schuette collected two specimens at Kewaunee,
possibly of this species, but due to their immature fruits, making
determination impossible, they are omitted from this report. In
ballast along railroads, and in wasteplaces. Flowering season
June and July.
Native of Asia and western America ; adventive eastward.
3. HACKELIA Opiz.
(See I. M. Johnston. Restoration of the genus Hackelia.
Contr. Gray Herb. Harvard Univ. 68: 43-48. 1923.)
a. Nutlets globose and equally short-glochidiate over the entire back.
Leaves mostly 2 or more cm. wide . 1. H. virginiana
aa. Nutlets globular to pyramidal and not equally glochidiate over the entire
back; leaves less than 2 cm. wide.
b. Nutlets with prickles only on the margin; back of nutlet deltoid-
ovate . . .2. H. deflexa
bb. Nutlets with prickles on the margin, with a few along the middle;
back of nutlet deltoid in shape . 3. H. deflexa var. americana
278 Wisconsin Academy of Sciences , Arts and Letters
1. Hackelia virginiana (L.) I. M. Johnston. (Beggar’s Lice or
Virginia Stickseed)
Lappula virginiana (L.) Greene, (1891).
(Map 5). This is a typical woodland species occurring
throughout the southern two-thirds of the State, north to Bar¬
ron and Langlade Counties. I have found it to be most abundant
in beech and sugar maple woods, rarely it can be found in shrub¬
by thickets, waste ground, and along roadsides. Flowering sea¬
son June 25 to July 31. Flowers small, blue.
2. Hackelia deflexa (Willd.) Opiz. (Nodding Stickseed)
Lappula deflexa (Wahl.) Garcke, (1893).
(Map 6). Occasional in the northeastern and southwestern
parts of the State on limestone cliffs, bluffs and outcroppings,
along roadsides, in waste places, and in open woods and thickets.
Flowering throughout June and the first week of July. Flowers
blue.
Native of Eurasia; naturalized in North America.
3. Hackelia deflexa (Willd.) Opiz. var. Americana ("Gray)
Fernald & Johnston.
(See Rhodora 26: 124-125. 1924)
Lappula deflexa w ar. americana (Gray) Greene, (1891).
(Map 7). Rare in the State. Most of the collections were
made in the northeastern part, with a few collections from the
western part of the State along the Mississippi River. Open
woods and thickets and on limestone cliffs and bluffs. Flowering
throughout the month of June.
4. AMSINCKIA Lehm.
(See Macbride, J. F. A Revision of the North American
species of Amsinckia. Contr. Gray Herb. Harvard Univ. n.s.
xlix. 1-16 (1917) )
1. Amsinckia lycopsioides Lehm. Amsinckia
(Map 8). Introduced into Wisconsin from California, it has
been collected at four stations in the State. Waste ground along
railroad tracks. Flowers pale yellow. Flowering in June and
the first two weeks of July.
5. SYMPHYTUM (Tourn.) L.
a. Stems and inflorescence glabrate or hirsute, the hairs not prickle-like or
barb-like, but longer, more slender, and of more or less uniform thick-
Kruschke— Flora of Wisconsin. XXXI . Boraginaceae 279
ness throughout; tips of corolla-lobes recurved; leaves decurrent, the
well-developed wing extending down the stem ........... .1. S. officinale
aa. Stems and inflorescence covered with short, recurved, prickle-like or
barb-like hairs laterally compressed and very much broadened at the
base; tips of corolla-lobes erect; leaves not decurrent or obscurely so _
. . . . . . . 2. S. asperum
l. Symphytum officinale L. (Common Comfrey)
(Map 9). Rare; specimens have been collected at eight dif¬
ferent stations, five of them within the city limits of Milwaukee.
Along railroad tracks and bordering waste land, vacant lots, and
fields. Flowering specimens have been collected from June 8 to
August 11. Flowers rarely white, usually purple. The latter
color-form was known in Europe, since it is mentioned in Hegi’s
Flora von Mittel-Europa as a distinct variety— -S. officinale L.
var. purpureum Pers. It seems preferable to rank it as a forma
rather than a distinct variety. The colored form was collected
at three stations where collections were also made for the white
form.
Introduced from temperate Europe.
2. Symphytum asperum Lepechin. (Rough Comfrey) (See Rho-
dora 18 : 23-25. 1916).
Symphytum asperrimum Bonn., (1806).
(Map 9). Only one station reported for the State. A single
specimen was collected in Racine, Racine County, in 1915 by
Mrs. F. J. Pope. This specimen is in the herbarium of the Uni¬
versity of Wisconsin. Flowers purple.
Introduced into America from Europe.
6. LYCOPSIS L.
1. Lycopsis arvensis L. (Small Bugloss)
(Map 10). Collected in three counties bordering Lake Mich¬
igan where it was found growing in dry, cultivated fields and
waste places. Field data for the specimens collected are very
incomplete, no mention being made as to its abundance in any
one of the localities where it was collected. Flowers blue. Flow¬
ering season June 10 to July 25.
Adventive from temperate Europe.
7. ANCHUSA L.
1. Anchusa officinalis L. (Common Alkanet)
(Map 10). Mr. Fuller of the Public Museum collected this
280 Wisconsin Academy of Sciences, Arts and Letters
species in Milwaukee, in a vacant lot, where it was growing as a
garden-escape. Flowering in July. Flowers deep blue to pur¬
plish-blue. Native of temperate Europe and of Asia Minor.
Commonly grown in gardens in this country.
8. MYOSOTIS (Rupp.) L.
a. Fruiting pedicels as long or longer than the calyces; calyx not 2-lipped;
corolla mostly more than 2 cm. broad.
b. Calyx with few, short, closely appressed hairs, none of which are
hooked or gland-tipped; flowers blue; aquatic or marsh plants,
c. Calyx-lobes much shorter than the tube; limb of corolla 5-9 mm.
broad; style much exceeding the nutlets and about as long as the
calyx-tube . . ..1. M. scorpioides
cc. Calyx-lobes about as long as the tube; limb of corolla rarely as
much as 5 mm. broad; style definitely exceeded by the nutlets and
shorter than the calyx-tube . 2. M. laxa
bb. Calyx densely covered with spreading hairs, some of them hooked or
gland-tipped, at least at the base of the calyx; fruiting-calyx open;
flowers usually light blue, occasionally white; corolla 1.5 to 4 mm.
broad; plants of well-drained soil . 3. M. arvensis
aa. Fruiting pedicels shorter than the calyces; calyx 2-lipped, unequally and
deeply 5-cleft; flowers white and inconspicuous; corolla 1-2 mm. broad;
calyx hairs hooked or gland-tipped; plants growing in dry soil .
. 4. M. vema
l. Myosotis scorpioides L. (True Forget-me-not)
(Map 11). Most collections of this species have been made
in eastern Wisconsin, especially in the counties bordering Lake
Michigan. Several collections have, however, been made in the
western and northern parts of the State. Common at all stations
reported, growing in wet ground in swamps, sloughs, ditches,
and borders of creeks, rivers, and lakes. On several occasions
1 have seen it growing in wet, alluvial soil on bottoms of dried-up
streams. Flowering season extending throughout June, July and
August.
Naturalized from Europe; frequently cultivated.
2. Myosotis laxa Lehm. (Smaller Forget-me-not)
(Map 12). Rare in the State. This species has been collected
only along the Wisconsin River as far east and north as Colum¬
bia County. It prefers wet shores and shallow water and also
wet, marshy sloughs and ditches. Flowering season from May
to August.
3. Myosotis arvensis (L.) Hill. (Field Scorpion Grass or
Mouse Ear)
Kruschke — Flora of Wisconsin. XXXI. Boraginaceae 281
Cynoglossum officinale
Lappula echinata
Lappula Redowskii
■vu.r» occidental! s
Wisconsin Academy of Sciences, Arts and Letters
Ansinckia lycopsioides
© Symphytum officinal®
Symphytum ©sperum
@ Lycopsis aT^ensis
*§i Anchusa officinalis
i^osotis laxa
Kruschke — Flora of Wisconsin. XXXI. Boraginaceae 283
Wisconsin Academy of Sciences, Arts and Letters
Lithosperraum lati folium
Lithosperraum incleum
Lithosperraum cane scene
Lithosperraum croceum
23
24
Onosmodium moll©
var. occidental©
Onosmodium hispid! ssimum
Echiura vulgar©
Kruschke — Flora of Wisconsin . XX XL Boraginaceae 285
(Map 13). Collected in Racine, Sheboygan, and Door Coun¬
ties and also on Madeline Island in Ashland County. Dry ground
in old abandoned gardens, cemeteries, waste lots, and pastured
meadows. Flowering the last week in May through June and
July.
The white-flowered form was collected by C. F. Millspaugh
at Ephraim, Door County, June 9, 1913, along with the typical
form. Both types are mounted on the same herbarium sheet in
the herbarium of the Field Museum.
Native of Europe; introduced into North America.
4. Myosotis verna Nutt. (Spring or Early Scorpion Grass)
(See Rhodora 43:636. 1941).
Myosotis virginica (L.) BSP., (1888).
(Map 14). This species is pretty well confined to four coun¬
ties bordering the Wisconsin River from northern Juneau Coun¬
ty south and west to Grant County. Waupaca, Brown, and Jef¬
ferson Counties are also represented by one collection each.
Generally it seems to prefer sandstone or quartzite, since in all
cases except one, it was found growing on quartzite cliffs and
bluffs, on sandstone bluffs and hills, and in sandy plains and pas¬
tures. The exception is the Brown County station, located in a
pasture just east of a limestone ledge. Flowering chiefly in May
and during the first three weeks of June.
9. MERTENSIA Roth.
(Williams. A monograph of the genus Mertensia in North
America. Ann. Missouri Bot. Gard. 24: 17-159, 16 fig. 1937)
a. Corolla trumpet-shaped, with limb barely 5-lobed, without crests in the
throat; filaments slender and much longer than the anthers; leaves
oblong to ovate, obtuse, glabrous on both surfaces; calyx glabrous .
. 1. M. virginica
aa. Corolla f unnelf or m - campa nula te, with crested throat and limb conspicu¬
ously 5-lobed; filaments flattened and as long or shorter than the anthers;
leaves ovate-lanceolate and taper-pointed, pubescent on both surfaces;
calyx pubescent . 2. M. paniculata
l. Mertensia virginica (L.) Link. (Virginia Bluebell)
(Map 15). Distribution of this species is confined to the
southwestern part of the State where it grows chiefly in alluvial
soils of wooded river bottoms (Mississippi, Wisconsin, Kicka-
poo, Sugar and Pecatonica Rivers). Fassett collected two speci¬
mens in Grant County, one growing on dry, wooded talus along
286 Wisconsin Academy of Sciences, Arts and Letters
the Mississippi River bluffs and the other growing in rock crev¬
ices on a bare limestone bluff. It is also reported from St. Croix
Falls, and in Minnesota, opposite La Crosse. Flowers light blue,
occasionally tinted with rose-purple, the latter being especially
pronounced in the flower-buds. Flowering season May.
2. Mertensia paniculata (Ait.) G. Don. (Tall Lungwort)
(Map 16). Fairly common on the south shore of Lake Su¬
perior. It has also been collected at two other stations in the
northern part of the State: Hurley in Iron County and Long
Lake in Florence County. All of the specimens are from wooded
river bottoms, wooded banks of streams, and from wooded
swamps. Flowers light blue, sometimes tinged with rose-purple.
Flowering season June and the first three weeks of July.
10. LITHOSPERMUM (Tourn.) L.
Flower Key to Species
a. Corolla as long as or slightly exceeding the calyx; flowers white to
greenish-white or yellowish.
b. Branch-veins of leaf inconspicuous, only the midrib evident; flowers
white to yellowish- white; corolla -lobes glabrous on the outer surface
. 1. L. arvense
bb. Branch -veins of leaf conspicuous; flowers greenish-white to greenish-
yellow or yellow; corolla-lobes pubescent on the outer surface,
c. Only a few distinct veins, these somewhat obscured by the dense
pubescence; leaves 6-12 (rarely -14 or more) mm. broad, firm,
lanceolate, and acute; pubescence on upper leaf-surface of varying
length, the bases of the larger hairs often expanded and scale-like;
flowers greenish- white to greenish-yellow; corolla not over 4.5
mm. long; calyx-lobes 3.5 mm. or less long . 2. L. officinale
cc. Veins more numerous and more prominent; leaves 12-45 (chiefly
15-35) mm. broad, thin, ovate, and acuminate; pubescence on upper
leaf-surface consists of numerous shorter hairs with fewer dis¬
tinctly longer hairs, the bases of the hairs occasionally expanded
but rarely scale-like; flowers yellow; corolla 4.5-8.S mm. long;
calyx 3.5-6 mm. long . 3. L. latifolium
aa. Corolla several times longer than the calyx; corolla light yellow to deep
orange-yellow.
d. Leaves ribbon-like, acute, appressed canescent-pubescent; flow¬
ers light yellow; corolla-tube narrow, 14-35 mm. long; corolla-
lobes finely toothed . 4. L. incisum
dd. Leaves chiefly oblong to lanceolate or narrow-lanceolate, rarely
ribbon-like, more or less obtuse; flowers light to deep orange-
yellow; corolla-tube broader and less than 14 mm. long; corolla-
lobes entire.
e. Corolla-tube naked at the base inside; calyx-lobes 2-6 mm.
Kruschke — Flora of Wisconsin. XXXI. Boraginaceae 287
long; leaves closely appressed canescent-pubescent above;
flowers sessile or nearly so; flowers orange -yellow .
. . y . . . . . . 5. L. canescens
ee. Corolla-tube hairy at the base inside; calyx-lobes 6-13 mm.
long; leaves loosely appressed-pubescent above; hairs fewer
and more coarse and stiff than in the previous species, each
hair with a more or less papillose base; flowers distinctly
peduncled; flowers usually light yellow, occasionally light
orange-yellow . . . 6. L. croceum
Fruit Key to Species
a. Nutlets brown or dull gray, rough -wrinkled or densely tuber cled .
. . . 1. L. arvense
aa. Nutlets smooth and shining, white to ivory,
b. Branch-veins of leaf conspicuous.
c. Nutlets 2-3.5 mm. long; leaf -veins few and somewhat obscured by
the dense pubescence; leaves 6-12 (rarely -14 or more) mm. broad,
firm, lanceolate, and acute; pubescence on upper leaf-surface of
varying length, the bases of the larger hairs often expanded and
scale-like . 2. L. officinale
cc. Nutlets 3.5-4. 5 mm. long, broader and more plump; leaf-veins more
numerous and more prominent; leaves 12-45 (chiefly 15-35) mm.
broad, thin, ovate, and acuminate; pubescence on upper leaf-
surface consists of numerous shorter hairs with fewer distinctly
longer hairs, the bases of the hairs rarely expanded and rarely
scale-like . 3. L. latifolium
bb. Branch-veins of leaf not conspicuous.
d. Leaves linear or ribbon-like, mainly S.5-4.5 mm. long, less than
5 mm. wide, acute, appressed canescent-pubescent; nutlets usu¬
ally punctate . . . 4. L. incisum
dd. Leaves chiefly oblong to lanceolate or narrow-lanceolate, rare¬
ly ribbon-like, more or less obtuse; fruits smooth,
e. Calyx-lobes 2-6 mm. long; fruit-clusters more or less ses¬
sile; nutlets 2-3 mm. long; leaves closely appressed canes¬
cent-pubescent above . . . 5. L. canescens
ee. Calyx-lobes more than 6 mm. long; fruit-clusters distinctly
peduncled; nutlets 3.5-4 (rarely 3-4.5) mm. long; leaves
loosely appressed-pubescent above; hairs fewer and more
coarse and stiff than in the previous species, each hair with
a more or less papillose base . 6. L. croceum
1. Lithospermum arvense L. (Corn Grom well)
(Map 17). Very rare, only three stations reported for the
State: Marinette in Marinette County, Sheboygan in Sheboygan
County, and Janesville in Rock County. The Marinette collection
was made along a railroad embankment; the other two collec¬
tions bore no data regarding specific habitat. Flowering season
May and early June.
288 Wisconsin Academy of Sciences, Arts and Letters
Native of Europe and adjacent Asia and Africa; introduced
in North America.
2. Lithospermum officinale L. (Common Gromwell)
(Map 18). Rare; collections have been made in only four
counties in eastern Wisconsin; roadsides, fields, and waste
ground. Flowering season May and early June.
Native of Europe and the Mediterranean region; introduced
in North America.
3. Lithospermum latifolium Michx. (American Gromwell)
(Map 19). Eastern, southwestern, and western Wisconsin, as
far north as Brown and Pierce Counties ; in mesophytic woods,
borders of woodlots, and open ground. An uncommon species,
usually found growing in small, sparsely scattered colonies. On
the several occasions that I have seen this species it seemed to
prefer sandy loam banks and slopes. The fact that it branches
so freely and reaches a height of 2 to 3 feet gives it an almost
shrub-like appearance. Flowering season May 20 to August 5.
4. Lithospermum incisum Lehm. (Narrow-leaved Puccoon)
(KewBull. 2: 59. 1934)
Lithospermum angustifolium Michx., (1803).
Lithospermum linearifolium Goldie, (1822).
(Map 20). North to Barron, Portage, and Sheboygan Coun¬
ties. It is rather common in the southern part of the State, espe¬
cially in Sauk, Dane, Rock, and Walworth Counties, less frequent
in the Western part and rare in the eastern counties. Dry sandy
soil of hillsides, bluffs, prairies, fields, and along railroads, in
open ground. In southeastern Wisconsin I have seen several
colonies on the Lake Chicago beach, growing in dry sandy soil
at the border of open oak groves. Flowering season May and
early June.
5. Lithospermum canescens (Michx.) Lehm. (Hoary Puc¬
coon)
(Map 21). Fairly common in southern and western Wiscon¬
sin and infrequent in the eastern part of the State. No collec¬
tions have been made in the north central area north of Portage
County, and between Sawyer and Marinette Counties. It prefers
sandy soil, growing in prairies, open woods, roadsides, and along
the railroad right of ways. Flowering season May and June and
occasionally in early July.
Kruschke — Flora of Wisconsin . XX XL Boraginaceae 289
6. Lithospermum croceum Fernald. (Hairy Puccoon) (Rho-
dora 37: 829. 1935).
Lithospermum carolinianum Lam., (1791).
Lithospermum hirtum Lehm., (1818).
Lithospermum Gmelini Hitchc., (1894), of Gray, Man., ed. 7.
Lithospermum carolinense (Walt.) MacMill, (1892), of Brit¬
ton and Brown, Illus. Flora, ed. 2.
(Map 22). Distribution quite similar to that of the previous
species; infrequent to fairly common in the southern half and
western parts of the State, especially in the counties bordering
the Wisconsin River; rare in the eastern part of the State. In
dry ground, especially sandy soil, in open woods, prairies, in
hilly fields and on bluffs and hilly slopes bordering lakes and
streams, and along roadsides and railroad right of ways. Flow¬
ering during the latter half of May and June, also in July, rarely
during the month of August.
11. ONOSMODIUM Michx.
a. Leaves lanceolate-ovate, mostly 1-2 cm. wide; pubescence of numerous
silky-gray to grayish-white, fine, short, appressed hairs, the individual
hairs less than 1.5 mm. long and not conspicuous to the naked eye; nut¬
lets rounded and not constricted at the base to form a collar . . .
. 1.0. nolle var. occidentale
aa. Leaves mostly ovate, 1.5-4 cm. wide; pubescence of white to yellowish-
white coarse bristles, mostly spreading (especially on stem, branches,
and on the rib-like veins on under surface of the leaves), the bristle-like
hairs more than 1.5 mm. long and very conspicuous to the naked eye
(pubescence on the leaves consists of numerous long hairs with fewer
distinctly shorter hairs); nutlets constricted at the base to form a short
neck or collar . . . . . . 2. O. hispidissimum
l. Onosmodium molle var. occidentale (Mack.) I. M. Johns¬
ton. (Western False Gromwell)
Onosmodium occidentale Mack., (1905).
(Map 23). Only two stations reported for the State, one at
Fountain City, Buffalo County, the other at Rutledge, Grant
County. All specimens collected at these stations lacked date re¬
garding habitat and frequency. Flowers sordid yellow. Flower¬
ing season the latter half of June and July.
2. Onosmodium hispidissimum Mack. (False Gromwell)
(Map 23). This species has been collected in the southern
and eastern parts of the State. None of the collections bear any
290 Wisconsin Academy of Sciences , Arts and Letters
data as to frequency and habitat. Flowers sordid yellow. Flow¬
ering season late June and July, rarely in August.
12. ECHIUM (Tourn.) L.
1. Echium vulgare L. (Blueweed or Viper’s Bugloss)
(Map 24). Abundant in places in eastern Wisconsin in dry,
gravelly to sandy-gravelly soil of morainal hills, sloping embank¬
ments, ridges and knolls, in fallow fields, waste ground, road¬
sides, pastures, hay fields, railroad right of ways and occa¬
sionally in farmyards. The largest colonies I had ever seen were
south of Barton near the Milwaukee River in Washington Coun¬
ty, and in Fond du Lac County four to five miles north of Ke-
waskum in fields bordering County Highway G, and in fields
bordering the road entering the Kettle Moraine State Forest at
Mauthe Lake. During the past four years I have made frequent
trips to this central kettle moraine area when this species was in
flower and have observed it to be spreading gradually in all di¬
rections. It has already spread to the extreme southwestern part
of Sheboygan County.
This species has also been collected in Dane County, near Pine
Bluff. The flowers are deep, brilliant blue in color, occasionally
rose-pink to rose-purple. The flower-buds are more or less rose-
pink in color. I have seen several plants where all the mature
flowers had this roseate or rose-pink color. Smith and Fuller
collected a specimen with white flowers at Mauthe Lake in Fond
du Lac County, July 12, 1927. The specimen #1772 is in the
herbarium of the Milwaukee Public Museum. This white-flow¬
ered form was known in Europe, since it is referred to in Hegi’s
Flora von Mittel-Europa V 3: 2193.1. Rydberg, in his Flora
of the Prairies and Plains of Central North America, also men¬
tions the white-flowered form. Flowering season the latter half
of June and July.
Naturalized from Europe.
PARASITES OF NORTHERN WISCONSIN FISH
Ralph V. Bangham
College of Wooster
The data presented are the result of a fish parasite survey
carried on during the spring and summer of 1943 as a joint
project between the University of Wisconsin and the Biology
Division of the Wisconsin Department of Conservation. Earlier
studies by Cross (1933, 1934, 1935, and 1938) gave some idea of
the parasitism of fish in certain of the lakes covered in the pres¬
ent survey. With the exception of this work by Cross and some
earlier preliminary work by Dr. C. A. Herrick, the fish para¬
sites of northern Wisconsin have not been investigated. Com¬
plaints to the conservation department concerning the presence
of fish parasites, especially larval flukes encysted in the flesh or
skin, led to the instigation of the present study.
Fish were obtained from over forty different locations, chief¬
ly lakes. The parasites of 1,330 fish belonging to 38 different
species are included in this report. These fish were obtained by
several methods: by hook and line fishing, from gill and fyke
nets, by seining, and by the use of minnow traps. Twelve hun¬
dred and thirty-nine, or 93.2 per cent of these fish carried at
least one species of parasite. The number of individuals para¬
sitized was rather high when compared to the results of previous
surveys. Bangham and Hunter, (1939) reported a 60 per cent
infection from a study of parasites of Lake Erie fish. During
this survey of Lake Erie, 2,156 fish representing 79 species, were
examined and included more minnows and young fish than the
present investigation. In 1940 the writer examined 1,380 south¬
ern Florida fish belonging to 43 species and found 1,218 or 88.2
per cent parasitized with at least one form. In 1940 the author
reported on a 1939 survey of the Algonquin Park lakes (On¬
tario). Here 560 fish belonging to 22 species were examined for
parasites and 84.3 per cent were found to be infected.
In these last two surveys the numbers of parasitized fish
were increased due to the presence of many strigeids belonging
to several different species and having a metacercarial stage
291
292 Wisconsin Academy of Sciences , Arts and Letters
encysted in the flesh, skin, or visceral organs of the host. The
definitive stage of these strigeids is carried by a fish-eating bird
and the cercariae develop within a snail. In the present study
encysted strigeids, encysted eye flukes and gill flukes accounted
for the major portion of the fish infections.
The degree of infection varied widely in different lakes and
also among species of fish. The chemical, biological and physical
characteristics of the habitat of the host appear to have a rather
marked effect on distributions of the parasites (Table III). In
seepage lakes with soft water, snails were reduced or absent, and
digenetic flukes were restricted probably as a result of the lack
of their primary hosts. In these lakes Acanthocephala are re¬
duced or absent but immature nematodes ( Camallanus sp.) were
frequently encountered. In lakes where walleyed pike were
found, larval Triaenophorus sp. cysts were taken in large num¬
bers, especially from yellow perch.
In this report a list of the areas from which fish were ob¬
tained giving location, size, type (seepage, flowage, or natural
lake with inlet and outlet) and chemical data, especially with
relation to the amount of carbonates, are included (Table III) .
Most of the fish were examined while fresh or were placed
on ice and examined the following day. Freezing relaxed the gill
flukes which were then preserved in 5 per cent formalin. The
exterior, skin, flesh, eyes, mouth, and visceral organs were ex¬
amined. Parasites were picked out for future study under a
binocular microscope. Then a 0.7 per cent solution of sodium
bicarbonate was used which helped dissolve the mucus and aided
in cleaning the worms remaining from the preliminary examina¬
tion. The larger cestodes, nematodes, and leeches were killed in
10 per cent formalin then preserved in a 5 per cent formalin
solution. Acanthocephala were allowed to die in water before
being preserved. The parasites which were not recognized in the
preliminary study were stained in Delafield’s Haematoxylin.
This investigation was jointly supported by funds from the
Wisconsin Alumni Research Foundation and the Wisconsin Con¬
servation Department. The writer acknowledges the assistance
and cooperation of Dr. Edward Schneberger, Chief Biologist of
the State Conservation Department, in helping to plan the study
and for his counsel and interest during its progress.
Assistance in collection of fish and information on the nature
of lakes investigated was given by Mr. Thomas H. Flanigon, area
Bangham — Parasites of Northern Wisconsin Fish 293
biologist of the State Conservation Department at Woodruff,
Wisconsin, where most of the field studies were conducted. Sev¬
eral men in the fisheries division at Woodruff also assisted in the
collection of fish used in the survey.
Mr. D. John O'Donnell, area biologist located at Spooner,
Wisconsin, assisted in the collection of fish and offered facilities
of his laboratory during the period spent in that region (north¬
western Wisconsin).
Dr. Chancey Juday gave information useful to this study as
the result of his long study of lakes from which many of the fish
being reported on, were secured. The interest, advice, and assist¬
ance of Dr. C. A. Herrick is much appreciated.
All of the identifications in the present report are those of
the author except for the parasitic copepods. Dr. Wilbur M. Tidd
of Ohio State University assisted in determining the species of
Table I. Parasites frequently encountered.
Number of
species of fish
Trematoda
Azygia angusticauda . 12
*Clinostomum marginatum . 7
Cryptogonimus chyli . 7
*Diplostomulum schewringi . 5
*Diplostomulum sp . 5
Gyrodactyloidae . 18
*Neascus sp . 19
* Pos thodip losomum minimum . 7
Cestoda
*Proteocephalus ambloplitis . . 8
**Proteocephalus pearsei . 7
Proteocephalus pinguis . 5
*Triaenophorus nodulosus . 12
Nematoda
*Agamonema sp . 6
**Camallanus sp . 9
Contracaecum sp. . . 5
Dichelyne cotylophora . 5
Spinitectus carolini . 5
**Spinitectus sp . . . 6
Acanthocephala
*Leptorhynchoides thecatus . 7
Leptorhynchoides thecatus . 14
Neoechinorhynchus cylindratus . 7
Pomphorynchus bulbocolli . 7
Copepoda
Ergasilus caeruleus . 10
Protozoa
Myxosporidia . 8
Hirudinea
Illinobdella sp . 6
294 Wisconsin Academy of Sciences, Arts and Letters
the latter. The gill flukes were submitted to Dr. John D. Mizelle
of Notre Dame University and have not yet been identified to
species.
Thirty-three species of parasites were found in but a single
host species of fish. These were mainly adult forms. In Table I
which follows, parasites which were encountered in more than
Table II. Summary of hosts, habitats, and number of parasite species.
Total fish examined
Total fish infected
Total percent infected
1,330
1,239
93.2
Number of different
species — 79
(more to be identified)
Bangham — Parasites of Northern Wisconsin Fish 295
five species of fish are listed. As in later tables encysted larval
forms are indicated by a single asterisk (*), while immature
stages within the digestive tract are marked by a double aster¬
isk (**). A moderate to heavy infection of cysts of Neascus sp.
Table III. Habitats from which fish were obtained.
Bound
Carbon
Area Dioxide
296 Wisconsin Academy of Sciences , Arts and Letters
was obtained from fish of 19 species. These infected fish had the
tiny pigmented cysts in their skin and flesh and were easily ob¬
served by fishermen as were the larger yellow “grubs” of Clinos-
iomum marginatum , embedded in the flesh and about the gill
region of the host. These disfiguring parasites are not capable
of becoming established in man even though the fish were im¬
properly cooked. No parasites which can be transferred from
fish to man were encountered although it is possible that the
broad tapeworm of man, Diyhyllobothrium latum may be occa¬
sionally found in the area covered by the survey.
The gill flukes of which there were numerous species are tiny
but often appear to cause considerable damage to the delicate
gills of the host.
The remaining forms, listed as frequent parasites, were
found within the digestive tract, as metacercariae in the eyes or
as encysted stages in the gonads, liver or mesentery.
In Table II the species of fish are listed giving numbers ex¬
amined, different habitats and the number of parasite species
found in the course of the survey.
Table III gives the county, water area and character of the
body of water from which fish were obtained for examination.
In the data which follow on distribution of parasites in the
thirty-eight species of fish, the listing of parasites and degree of
parasitism is indicated by asterisks and habitat is given in tabu¬
lar summary. This is followed by a short discussion in cases
where several fish were examined from different locations.
Key: * encysted state; ** immature form in digestive tract; 1 1-9 parasites;
2 10-49 parasites; 3 50 parasites and over.
(1) Amia calva Linn, young
Bowfin
Woodruff Hatchery Pond 11
Examined 8 8
Infected 8 8
**Bothriocephalus sp. I1
**Haplonerna immutatum l1
Macroderoides typicus 8s
**Proteocephalus perplexus 81
**Spiroxys sp. I1
No adult bowfins were examined. The eight young specimens measured
from 6.1 to 7.2 centimeters and all the parasites were immature except for
flukes, M. typicus.
Bang ham — Parasites of Northern Wisconsin Fish
297
(2) Leucichthys artedi clarerisis Koelz
Clear Lake cisco
Johnson Lake Clear Lake
Examined 12 10 2
Infected 10 10
Proteocephalus laurel 63
42
Cisco were only taken from two lakes during the survey and but one
species of parasite, P. laruei , was taken. These small cestodes were very
numerous in most of the Johnson Lake cisco, but the Clear Lake fish were
negative. Cross (1938) reports on the parasites of 128 cisco taken from Clear
Lake in 1931 and 1932. Fourteen of this number carried three species of
parasites.
(3) Salmo trutta fario Linn.
Brown trout
Examined 12
Infected 4
Crepidostomun cooperi
Rocky Run Creek — Brule River tributary
12
4
l1
(4) Salmo gairdnerii irideus Gibbons
Rainbow trout
Minocqua
Thoroughfare
1
1
Examined 4
Infected 2
Phyllodistomum sp.
* ^Proteocephalus pinguis l1
Spooner
Hatchery
2
1
l1
Little Brute
River
1
(5)
Salvelinus fontinalis fontinalis (Mitchill)
Brook trout
Marathon County
Four-Mile Creek
Examined 14 4
Infected 4 4
Crepidostomum cooperi 32-!3
*Leptorhynchoides
thecatus
N eoechinorhynchus sp.
Little Brule
River
2
Brule
Hatchery Creek
* Proteocephalus pinguis
Hie brook trout from Four-mile creek were young adults and those from
the other two areas were smaller, from 3.9-12 cm. in length.
298 Wisconsin Academy of Sciences, Arts and Letters
(6) Catostomus commersonnii commersonnii (Lacepede)
Common white sucker
(6) Nine of the parasite species were only taken from common suckers in
one location. Large numbers of glochidia were carried on the gills of the
sucker from the Lake Minocqua Thoroughfare, examined May 25. All fish of
other species with glochidia were secured in the early part of the survey.
P. nodulosa was found in galleries in the connective tissue of the pectoral fins
of 5 of the suckers taken from Blue Lake. There were from 1 to 4 in each
host, § being female specimens full of eggs. O. lanceatum was found on the
gills of common suckers from 4 lakes. This form has been previously reported
from suckers taken at Frederick Creek, Constantia, N. Y. by Mueller (1934)
Bangham — Parasites of Northern Wisconsin Fish 299
and from the same hosts in the Algonquin Park Lakes, Bangham (1940).
G. catostomi, O. macilentus, T. attenuatum , and cysts of T. nodulosus were
forms encountered with greatest frequency in suckers examined from the
different areas. P. bulbocolli was the only parasite secured from the Yellow
River Flowage at Spooner. From 200 to 300 individuals of this species were
found in each of these fish with their spiny proboscides deeply embedded in
the intestines of their host. Five of the 10 young suckers from Big Lake in
the Brule River carried large numbers of black strigeid cysts, Neascus sp.
These fish were liberally peppered with these cysts.
Two gill flukes were the only parasites secured from 10 young carp
examined from Lake-du-Bay.
(9) Rhinichthys atratulns meleagris Agassiz
Western blacknose dace
Brule River
Woodruff Hatchery Brule River Ranger
Marsh Pond Headwater Station
Examined 9 11 7
Infected 6 1 5
Acanthocephala l1
* Neascus sp. I1
* *Rhabodochonia sp. 41
*Tetracotyle sp. 21
(10) Chrosomus eos Cope
Northern redbelly dace
Woodruff Hatchery
Marsh Pond
Examined 10 10
Infected 8 6
*Clinostomum marginatum l1
*Neascus sp. 41
**Spiroxys sp. 21
300
Wisconsin Academy of Sciences , Arts and Letters
(11) Notemigonus crysoleucas auratus (Raf.)
Western golden shiner Moose Lake
Examined 2 2
Infected
(12) Notropis cornutus frontalis (Agassiz)
Northern common shiner
Trout Lake Snake Lake
Examined 4 2 2
Infected 3 2 1
*Clinostomum marginatum l1
*Neascv,s sp. 21 l1
(13) Notropis anogenus Forbes
Pugnose shiner
Madeline Lake
Examined 1 1
Infected
(14) Pimephales promelas promelas Raf.
Northern Fathead minnow
Examined 1
Infected 1
*Neascus sp.
(15) Hyborhynchus notatus (Raf.)
Bluntnose minnow
North Two Lake
Examined 16 9
Infected 6 5
*Cestode 51
*Neascus sp. 1
Madeline Lake
1
1
r
Shell Lake Johnson Lake
5 2
1
l1
(16) Ameiurus melas melas (Raf.)
Northern black bullhead
Moose Lake
Examined 3 3
Infected 3 3
Alloglossidium corti l1
Azygia angusticauda l1
Corollobothrium jimbriatum l1
l2
Dichelyne robusta l1
Gyrodactyloidae 2s
Leptorhynochoides thecatus l1
Myxobolus sp. I1
Pomphorhynchus bulbocolli l1
The three black bullheads were adults from 15-25 cm. in length. They
were taken in fyke nets from Moose Lake in Langlade County. All parasites
were found in small numbers; 1 to 3 per host except for 1 black bullhead that
had 12 C. jimbriatum and 2 hosts that had 10-20 gill flukes.
Ameiurus nebulosus nebulosus (LeSueur)
Northern brown bullhead
Bangham — Parasites of Northern Wisconsin Fish 301
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302 Wisconsin Academy of Sciences, Arts and Letters
(17) The majority of brown bullheads came from three locations while single
individuals were examined from three lakes. Four species of parasites made
up the largest number of those taken; gill flukes, A. geminus, C. fimbriatum ,
and P. staffordi. The last named form, P. staffordi a fluke found in the uri¬
nary bladder was taken in 8 of 65 brown bullheads during the survey of
Algonquin Park Lakes, Bangham (1940b). It was not secured from 23 Reel-
foot Lake brown bullheads, Bangham and Venard (1942) or from 22 Florida
bullheads, Bangham (1940). In one instance 25 P. staffordi were taken from
a single brown bullhead from Minocqua Thoroughfare.
(18) Ameiurus natalis natalis (LeSueur)
Northern yellow bullhead
Examined 1
Infected 1
Alloglossidium geminus
**Camallanus sp.
Corallobothrium fimbriatum
Dichelyne robusta
Gyrodactyloidae
*Proteocephalus ambloplitis
(19) Schilbeodes gyrinus (Mitchill)
Tadpole madtom
Lake-du-Bay
Examined 1 1
Infected 1 1
Gyrodactyloidae l1
Lake Minocqua Thoroughfare
1
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l2
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(20) Umbra limi (Kirtland)
Mud minnow
Woodruff
Hatchery Marsh
Examined 20 18
Infected 14 14
Bunoderina eucaliae 91
Hepaticola bakeri 81
r
*Neascus sp. I1
l2
Bass Lake
1
Lake Minocqua
Thoroughfare
1
All infected mud minnows were secured from a small marsh pond above
the Woodruff Hatchery. B. eucaliae has been previously reported as parasite
of the brook stickleback Miller (1936) and Bangham and Hunter (1939).
Brook stickleback from this pond also were infected with this small fluke.
H. bakeri was taken from 8 of the 20 mud minnows from the Woodruff marsh
pond. This small, delicate nematode was described by Mueller and Van
Cleave (1932) from Leucichthys artedi tullibee, Notemigonus crysoleucas and
Catostomus commersonnii. It was reported for a ling or burbot from Lake
Opeongo (Ont.) , Bangham (1940).
Mid Minocqua Yellow Cable Spooner Little Lake-
Lake Thor. River Lake Lake Brule du-Bay
Bang ham — Parasites of Northern Wisconsin Fish
303
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Triaenophorus nodulosus
304 Wisconsin Academy of Sciences , Arts and Letters
(21) P. pinguis was the form most commonly encountered. This cestode was
secured from all but 2 of the 34 northern pike. External strigeids, Neascus sp.
were found encysted in the skin and flesh of 18 of the northern pike. Gill
flukes were obtained from 13 of these fish. Hunter and Rankin (1940) report
on the parasites of the northern pike and pickerel from Connecticut. They
found in 11 E. lucius the following: A. angusticauda, P. pinguis , larval P.
ambloplitis and Spiruidae. They summarize in this report the parasites
found in recent New York State surveys, giving 11 different species for the
northern pike. Six species not reported from the northern pike from New
York were found in Wisconsin. These are, C. brachyurum, Haplonema sp.,
N. tenellus, Diplostomulum sp. C. cooperi and T. nodulosus. All of these were
found in some other species of fish during the survey. C. brachyurum , Hap¬
lonema sp, and a single adult T. nodulosus were taken from Spooner Lake
northern pike.
The tiny nematodes S. gracilis were found in this host in but one loca¬
tion, the Yellow River Flowage at Spooner.
(22)
Hybrid northern pike-muskellunge
Woodruff Hatchery
Examined 3 3
Infected 3 3
**Azygia angusticauda l1
*Clinostomum marginatum (free in intestine) l1
**Leptorhynchoides thecatus ll
* Neascus sp. I3
**Proteocephalus pinguis 21
(22) The hybrid northern pike-muskellunge were all secured from the
Woodruff Hatchery pond. They measured from 55.7 cm. to 65 cm. in length
and all but the encysted Neascus sp. were immature and in the digestive
tract.
(23) Esox masquinongy masquinongy Mitchill
Great Lakes muskellunge
Bang ham — Parasites of Northern Wisconsin Fish 305
All but three of the muskellunge were immature individuals from hatch¬
ery ponds at Woodruff and Spooner. These carried immature cestodes P.
pinguis and adults of a small species of flukes, C. chyli. Two adults from
Minocqua Thoroughfare and one from Carroll Lake had more numerous para¬
site species. In one muskellunge T. renicola were present in large numbers
in the urinary bladder. Mueller (1931 and 1932) described this form from the
urinary tract of the chain pickerel in Oneida Lake. Hunter and Rankin
(1940) report T. renicola from E. niger and E. americanus in Connecticut.
Another form belonging to the genus Trichodina was secured from the gills
of the host of T. renicola and also from the Carroll Lake muskellunge. This
appears to be a new species and if it proves to be it will be described else¬
where. A single large female Philometra sp. was taken from a cyst in the
body cavity of the Carroll Lake fish. Two species of Acanthocephala, L.
thecatus and N. tenellus, were present in small numbers in the intestines of
the adult fish. T. nodulosus cysts were found in moderate numbers in the
three adults.
(24) Fundulus diaphanus menona Jordan and Copeland
Island Lake
Examined 1 1
Infected 1 1
*Clinostomum marginatum l1
Gyrodactyloidae l1
*Neascus sp. I1
**Nematode l1
* *Neoechinorhynchus cylindratus l5
(25) Perea flavescens (Mitchill)
Yellow perch
More yellow perch were examined during the survey than any other
species of fish. These also came from a larger number of locations. From
the 261 infected perch the following forms were most frequently encountered:
Neascus sp. from 224, Gyrodactyloidae from 184, Diplostomulum scheuringi
from 151, larval P. pearsei from 147, C. marginatum cysts from 118, D. cotylo -
phora from 100 and T. nodulosus cysts from 77. All other parasite species
listed on the table were secured in from 1 to 50 of the yellow perch examined.
Adult flukes with the exception of one species of gill fluke were less
numerous than the larval forms. A. angusticauda, B. sacculata, C. cooperi
were secured in a part of the perch from 14 to 16 lakes, while C. chyli and an
unidentified form were taken from perch in one location.
Acanthocephala were not abundant in yellow perch. L. thecatus was
found in perch from 9 lakes while 7 lakes yielded perch infected with N.
cylindratus. P. bulbocolli was secured from 10 of the 21 perch examined from
Sweeny Lake.
D. cotylophora was the species of nematode secured most often from the
yellow perch. Spinitectus sp. was found in 32 perch from 8 locations and
larval Camallanus sp. from 14 from 6 lakes. A mature encysted specimen of
P. cylindracea was secured from a Trout Lake yellow perch.
(25) Perea flavescens (Mitchill)
_ Yellow perch _
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308 Wisconsin Academy of Sciences, Arts and Letters
P. pearsei was the only adult cestode obtained from the yellow perch.
Many also carried immature forms belonging to this species.
B. cuspidatus was secured as immature forms from half of the lakes where
yellow perch were examined. T. nodulosus was found in liver or mesentery
cysts from perch in 13 lakes and P. ambloplitis cysts were taken from a por¬
tion of the yellow perch in five lakes.
The parasitic gill copepod E. caeruleus was secured from a few perch in
three lakes.
The most abundant form, Neascus sp. was found as small integumentary
cysts about the size of a pin head, deeply pigmented on or just under the
scales. Others were often found deeper in the muscle septa. Some of the
yellow perch were liberally peppered with these tiny cysts. C. marginatum ,
the yellow grub was found most frequently encysted about the gills. Some
were in the flesh especially near the bases of the fins. Early in the survey
only large metacercariae were encountered but about the middle of July many
tiny cysts of this species were found. These were probably obtained this
season while the larger forms represented an infection of the previous year.
Late in July and in August many perch were found with larger metacer¬
cariae whose cyst walls were thin and the C. marginatum would emerge with
slight handling of the fish. It is the opinion of the writer that many of these
parasites may thus be lost from the host in this manner.
Two species of eye grubs were taken. The larger appeared to be D.
scheuringi and the smaller D. huronense. Both were found in the aqueous
and vitreous humor of the eye. Very few were secured from the lens.
P. minimum another strigeid was secured from but 11 perch in 4 lakes.
The infection with this form was light in all of these fish.
(26) Stizostedion vitreum vitreum (Mitchill)
Walleyed pike perch.
All of 84 walleyed pike perch from 15 lakes carried parasites. B. cuspi-
datus was found in 79 of these fish. This cestode was usually adult and often
many were found in one host. Along with this form was another cestode
species, P. stizostethi, first described by Hunter and Bangham (1933) from
the pike perch of Lake Erie. T. nodulosus , a third cestode, was found as
encysted larvae in the liver and viscera of 3 hosts from different lakes.
Three species of Acanthocephala were found in pike perch during the
survey. These were N. tenellus, L. thecatus and P. bulbocolli , N. tenellus was
widely distributed and often many individuals were found in one host.
A. aculeatus a monogenetic fluke was taken from the gills of 36 pike perch
while a second species of gill fluke was obtained from 2 hosts. Four species
of larval encysted flukes were encountered, the most frequently found being
skin cysts of U. ambloplitis. D. scheuringi was found in the eyes of 24 pike
perch. P. minimum and C. marginatum were secured from 1 and 3 hosts,
respectively. B. pusilla was the adult fluke most often found. This small form
was secured while Crepidostomum sp. and A. angusticauda were found in a
few of the pike perch.
Nematodes were not frequently taken. The three pike perch examined
from Bolling Stone Lake in Langlade County had from 50 to 250 Contracae-
Bangham — Parasites of Northern Wisconsin Fish 309
(26) Stizostedion vitreum vitreum (Mitchill)
Walleyed pike perch
310 Wisconsin Academy of Sciences, Arts and Letters
cum sp. free in their intestinal tracts. The only other place this nematode
was encountered in pike perch was in 1 of 7 from Pickerel Lake, a lake next
to Rolling Stone Lake. This infected host had 15 Contracaecum sp. Immature
Camallanus sp. and Spinitectus sp. were other nematodes secured from pike
perch.
The gill copepod E. caeruleus was taken from all of the pike perch from
Blue, Arbor Vitae, Trout and Snake Lakes but only single specimens were
examined from the last three lakes. Two of 16 from Minocqua Thoroughfare
and 4 of 9 from Butternut Lake also carried this parasitic copepod.
A leech I. moorei was found in the mouth and pharyngeal cavities of pike
perch from Blue, Squaw and Butternut Lakes. One host from Squaw and
two from Butternut had from 10-17 of these leeches, while the remainder
carried from 1-3 in the same part of the mouth cavity.
L. j ohnstonei, a filterable virus causing a disfiguring “Warty” skin, was
found in a single pike perch from Rolling Stone Lake.
The first pike perch examined on May 22 carried a number of glochidia
on its gills. No other glochidia were secured in pike perch examined later in
the season.
(27) Percina caprodes semijasciata (De Kay)
Northern log perch
Shell Lake — Washburn Co.
Examined 1 1
Infected
(28) Boleosoma nigrum nigrum (Raf.)
Central Johnny darter
Shell Lake
Examined 1 1
Infected
(29) Poecilichthys exilis (Girard)
Iowa darter
Madeline Lake
Examined 2 1
Infected 1 1
*Neascus sp. I2
(30) Micropterus dolomieu dolomieu (Lacepede)
Northern small mouth bass
Small mouth bass were obtained from 8 lakes in Vilas and Oneida
Counties and all of 44 individuals examined were parasitized. Thirty were
from Bass and Clear Lakes, which are seepage lakes with a low amount of
bound carbon dioxide. Clear Lake has an area of 922 acres while Bass Lake
contains about 30 acres. Eight species of parasites were carried by the 15
Bass Lake fish and there were 11 different parasite species in the Clear Lake
small mouth bass. Five of these were the same in the two lakes. Digenetic
trematodes were absent from the host in Bass Lake, as were Acanthocephala.
There was found in the Clear Lake fish 1 specie of Acanthocephala and
4 species of digenetic flukes but usually in smaller numbers than in the small
mouth bass from other lakes.
Minocqua Thoroughfare
1
Bang ham — Parasites of Northern Wisconsin Fish 311
(30) Micropterus dolomieu dolomieu Lacepede
Northern small mouth bass
3“
312 Wisconsin Academy of Sciences , Arts and Letters
From all areas larval P. ambloplitis was the parasite most frequently
encountered. Liver and visceral cysts were found in bass from all but one
of the lakes. Adults belonging to this species were secured from small mouth
bass from Nebish and Bass Lakes. P. fiuviatilis, a cestode usually found only
in stream bass, were secured from one Bass Lake specimen. Larval P. pearsei
were found in 20 small mouth bass from 6 lakes. The bass examined from
Blue Lake and from 60-70 adult P. pearsei as well as many larvae. Both the
P. fiuvia tills and P. pearsei mature in one fish after the procercoid has been
taken in with an infected copepod. Early B. cuspidatus larvae were found
free in the intestinal tract of the Blue Lake bass while 7 fish from Bass Lake
carried cysts of T. nodulosus.
Black cysts of Neascus sp. were found in the skin and flesh of 22 small
mouth bass out of the 29 examined from all of the lakes except Bass Lake.
Encysted C. marginatum, and Diplostomulum sp. were only taken from Clear
Lake bass. P. stunkardi was secured from one Clear Lake host, C. chyli
a small delicate fluke was found in large numbers in the pyloric caeca and
intestine of 5 bass from 4 areas. These were all of the bass examined from
those lakes. A. angusticauda was taken from the Madeline Lake bass while
two hosts from Little John and Nebish Lakes yielded Crepidostomum sp.
Gill flukes were found on 20 bass from 7 lakes.
Two species of Acanthocephala were found: L. thecatus in a part of the
bass from 6 areas and N. cylindratus from the bass of 3 lakes. Nematodes
were not found in large numbers. Immature Camallanus sp. were taken from
Blue and Bass Lake fish while S. carolini were found in small mouth bass
from Little John, Bass and Clear Lakes. A single infection was observed for
D. cotylophora from a Madeline Lake host, Contracacecum sp. from Nebish
Lake and an eye cyst with Philometra sp. from a Clear Lake host. Two bass
from Little John carried small numbers of C. catenata.
Two species of gill copepods were taken, A. micropteri on 10 hosts from
3 lakes and E. caerideus on 5 hosts from 4 lakes.
(31) Huro salmoides (Lacepede)
Large mouth bass
All of the large mouth bass carried parasites except four yearling fish
from Bullhead Lake. Almost one-third of the large mouth bass were finger-
lings.
A majority of the parasites belonged to the same species as those found
in the small mouth bass. The hosts were examined from a wider area. With
the exception of 4 bass bearing small numbers of Neascus sp. cysts, no
digenetic flukes or acanthocephalan species were obtained in 34 bass from
soft water seepage lakes. These lakes North Two, Little John Jr., Bass, and
Bullhead had a pH of 5.8 -5. 9 and the bound carbon dioxide ranged from
.7-1.6 P. P. M. It is possible that the first intermediate hosts of the missing
parasites had difficulty in survival.
The cestodes were the same as found in the small mouth bass; P. am¬
bloplitis encysted larvae in the viscera and immature forms in the intestine,
immature P. pearsei in the intestine, immature and adult P. fluviatilis in the
intestine of 11 hosts from Bass Lake and Minocqua Thoroughfare, immature
Bothriocephalus sp. from the intestine of 2 Bass Lake fish and encysted
Bangham — Parasites of Northern Wisconsin Fish 313
(31) Huro salmoides (Lacepede)
Large mouth bass
32
l1
314 Wisconsin Academy of Sciences , Arts and Letters
T. nodulosus. Sixteen of the 21 bass infected with this last form came from.
Bass Lake.
Gill flukes were commonly found on the majority of large mouth bass,
at least 2 species being present on some of the hosts. Many of the older bass
bore infections with Neascus sp. and a few were found to carry C. marginatum
and P. minimum. Light infections with Diplpstomulum sp. were found in the
eyes of 10 bass. The most common adult fluke was C. ehyli. A. angusticauda
and Crepidostomum sp. were also secured from a few individuals.
The following nematode species were taken from 1 to 16 bass during the
survey: S. carolini, Camallanus sp., C. catenta., D. cotylophora, P. cylindraca
and Agamonema sp.
L. thecatus and N. cylindratus were obtained from several of the bass.
In many instances both species were carried by the same host. The infections
were lighter and distributions more scattered than found in large mouth bass
studied by the investigator in other regions.
Gill copepods were scarce, A. micropteri being found on one host from
Bass Lake and E. caeruleus, on 8 bass from 3 areas.
(32) Lepomis gibbosus (Linnaeus)
Pumpkinseed, common sunfish
All of the 76 common sunfish from 15 areas bore parasites. Many
larval flukes were found in these fish. The black grubs, Neascus sp. were
encysted in 62 common sunfish taken from all of the areas except Bullhead
Lake. P. minimum, the white grub of the liver was found in 46 sunfish from
all but 3 lakes. C. marginatum, the yellow grub was encysted about the gill
cavities and in the flesh of 30 fish from 9 areas and D. scheuringi was taken
from the eyes of 39 sunfish in 8 areas. Adult flukes were less frequently
encountered. The following species were secured from a portion of the sunfish
examined: C. cooperi, C. comutum and A. angusticauda. Gill flukes were
present in many of the hosts.
Five species of cestodes were recorded for the common sunfish. One
adult B. claviceps was taken from a Nebish Lake sunfish. Immature B. cus-
pidatus were secured from single hosts in Lake Minocqua Thoroughfare and
Johnson Lake. P. pearsei adults were found in sunfish from 2 areas and
larvae of this species in the intestinal tracts of common sunfish from 4 areas.
P. ambloplitis cysts were taken from 7 sunfish in 3 areas. T. nodulosus cysts
came from 4 of the 24 fish examined from Lake Minocqua Thoroughfare.
S. carolini was the nematode species most frequently encountered, being
secured from 24 host while S. gracilis was taken from 5 individuals. D. coty¬
lophora, Contracaecum sp., Camallanus sp., C. catenata and Agamonema sp.
were found in a few hosts.
Acanthocaphala were not frequently taken, L. thecatus being taken from
15 common sunfish in 6 areas as adults and in addition an Island Lake host
yielded the encysted stage of this form. N. cylindratus was found in 2 hosts
and P. bulbocolli in a Johnson Lake sunfish. E. caeruleus was found on the
gills of 11 sunfish from Minocqua Thoroughfare, Island Lake and Johnson
Lake.
Bangham — Parasites of Northern Wisconsin Fish
(32) Lepomis gibbosus (Linnaeus)
Pumpkinseed, common sunfish
315
3 t 2
o' CS 3
Sh pq § u
to *
> K
ct
•S
*— >
,3
« J2
5
£
a> o
a s? a a
Examined 76
24 837 9171 311132
Infected 76
24 837 9171 3 11132
*Agamonema sp.
I1
Azygia angusticauda
2
Bothriocephalus claviceps
** Bothriocephalus cuspidatus
l1
l2
**Camallanus sp.
Capillaria catenata
l1
*Clinostomum marginatum
61
l1 1'
21
8s
**Contracaecum sp.
I1
Crepidostomum cooperi
41 i1 i2 r
21
l1 la
Crepidostomum comutum
61 21
4'1 l1
1*
Dichelyne cotylophora
31
*Diplostomulum scheuringi
Ergasilus caeruleus
Gyrodactyloidae (1)
la 21 l'1 51 l1 31 l1
102
2s
42
102 52 l2 r S2 l1 52
2s l2
52
l2 l3 23
7s 33 l3 42
Gyrodactyloidae (2)
l1 l1
Illinobdella sp.
I1
Leptorhynchoides thecatus
41 l'1 51
31
*Leptorhynchoides thecatus
*Neascus sp.
17
3s
42 l'1 l1 la 22 l1 l1 r I1 l1
53 62 l8 l2 32
23
Neoechinorhynchus cylindratus
Pomphorhyncus bulbocolli
*Posthodiplostomum minimum
3 l2 l2 l2 21 l3 l2
l1
ir
* Proteocephalus ambloplitis
31
Proteocephalus pearsei
l1
* * Proteocephalus pearsei
21 21
21 21
Spinitectus carolini
22
91 31 l1 21 l1
31
Spinitectus gracilis
‘Triaeuaphorus nodulosus
l1 l1
V
31
22
(33) Lepomis macrochirus macrochirus Rafinesque
Common bluegill
316 Wisconsin Academy of Sciences , Arts and Letters
Bangham — Parasites of Northern Wisconsin Fish
317
*Triaenophorus nodulosus _ l1 l1 _ 21 41 51 _ g1 191
318 Wisconsin Academy of Sciences , Arts and Letters
(33) All of 232 bluegills from 23 locations carried at least one species of
parasite. P. minimum the white grub of the liver was found in 133 bluegills.
The livers of 39 were riddled and many cysts were attached to the hearts of
these fish. Cysts were also found near the surface of the spleen and kidneys
of the heavily infected bluegills. Neascus sp. were found in pigmented cysts
in 166 bluegills, 14 of these hosts being heavily infected. Another larval
strigeid species was secured from mesentry cysts of 4 bluegills. D. scheuringi
was taken from the eyes of 55 hosts. C. marginatum was not often found in
bluegills, being taken in small numbers in 10 hosts from 6 areas. C. cooperi
was the adult fluke most frequently observed, being obtained from 61 blue¬
gills. C. comutum, C. chyli and A. angusticauda were found in a few hosts.
Cestodes were not abundant in these fish, encysted P. ambloplitis being
secured from 27 hosts in 14 areas. One adult B. claviceps was secured from a
Spooner Lake bluegill. Larval B. cuspidatus were taken from 3 bluegills and
larval P. pearsei from 9. S. carolini was the only species of adult nematode
frequently taken, being found in 104 bluegills from 17 locations. Immature
Camallanus sp. were found in 43 of these fish while Contracaecum sp. and a
larval encysted form were obtained from single hosts.
L. thecatus was secured from the intestine of 26 bluegills and as a larval
encysted form from a Carroll Lake host. N. cylindratus was found in 1 Car-
roll Lake bluegill while 4 of 8 bluegills from Casey Creek carried P. bulbo-
colli. Gill copepods were not frequently taken, A. micropteri being observed
and E. caeruleus on 15 from 5 areas.
(34) Ambloplitis rupestris (Raf.)
Rock bass
2s
Bangham — Parasites of Northern Wisconsin Fish 319
(34) Ambloplitis rupestris (Raf.) (continued)
Rock bass
320 Wisconsin Academy of Sciences , Arts and Letters
(34) All of 107 rock bass from 12 lakes were infected and the individuals
carried more parasites than were present in most other species of fish.
All but one carried cysts of Neascus sp. and 19 from 5 lakes were heavily
parasitized with these black cysts. P. minimum was found in fewer rock
bass, being secured from 56. Light to moderate infections of C. marginatum
were found in 36 hosts. Fifty rock bass yielded D. scheuringi and 56 carried
at least one species of gill fluke. C. chyli was secured in 49 rock bass from
all but two of the lakes. All of the fish bore large numbers of this small
fluke. C. cooperi was found in 10 rock bass from 6 lakes while single hosts
yielded A. angusticauda and Phyliodistomum sp.
P. pearsei was the cestode most frequently encountered. This small form
has both larval and mature stages within the intestinal tract of the host.
Adult P. pearsei were taken from 7 hosts and immature forms from 25. Imma¬
ture P. ambloplitis were secured from 4 hosts and encysted stages of this
form in 23 fish from 8 lakes. Pinkeye Lake yielded the majority of these.
An adult B. claviceps was taken in a rock bass from White Sand Lake and
2 Shell Lake hosts carried immature Bothriocephalus sp.
Immature Spinitectus sp. nematodes were found in 13 rock bass from
6 lakes, S. carolini adults in 9 hosts from 5 lakes and S. gracilis in 2 Shell Lake
hosts. Immature Contracaecum sp., probably C. brachyurum, were taken from
20 rock bass at Clear, Carroll and Pinkeye lakes. C. catenata was found in all
but one of the 21 Clear Lake specimens. Five were heavily infected with this
delicate form. D. cotylophora was taken in 3 hosts from different lakes.
Of the Acanthocphala L. thecatus was most frequently encountered, being
obtained in 44 rock bass in 8 lakes as adults and from 4 as encysted, immature
forms. N. cylindratus was taken from 14 rock bass.
Three species of parasitic copepods were secured; A. micropteri from 3
individuals in 2 lakes, E. elegans from a single Madeline Lake host and
E. caeruleus on 34 rock bass from 6 lakes.
(35) Promoxis nigro-maculatus (LeSueur)
Black crappie
The black crappies from 10 areas were less heavily infected than any
other species of Centrarchidae. Many of the same species of parasites were
found but in fewer hosts and with a low degree of infection. Gill flukes were
the most common parasitic form. Larval encysted flukes were not frequently
taken. D. scheuringi was secured from the eyes of 12 black crappies from
5 areas.
The 10 hosts from Lake-du-Bay yielded few parasites. This same condi¬
tion was true for many other species of fish examined from this large, newly
impounded, area. Many of the life cycles are not yet established. All black
crappies from this area have gill flukes and all but one had gill copepods,
E. caeruleus. A single host carried 4 eye flukes.
Bangham — Parasites of Northern Wisconsin Fish 321
(35) Promoxis nigro-maculatus (LeSueur)
Black crappie
(36) Cottus bairdii bairdii Girard
Millers thumb
Little Brule river Brule hatchery creek
Examined 2 1 1
Infected
(37) Eucalia inconstans (Kirtland)
Brook stickleback
Bass
1
1
l1
l1
322 Wisconsin Academy of Sciences , Arts and Letters
(38) Lota lota maculosa (LeSueur)
Burbot
Boot
1
1
r
11
i‘
Ancyrocephalus aculeatus Van Cleave and Mueller, 1932
Azygia angusticauda (Stafford, 1904)
Bucephalopsis pusilla (Stafford, 1904)
Bunodera sacculata Van Cleave and Mueller, 1932
Bunoderina eucaliae Miller, 1936
Clinostomum marginatum (Hud., 1819)
Crepidostomum cooperi Hopkins, 1931
Crepidostomum comutum (Osborn, 1903)
Crepidostomum sp.
Cryptogonimus chyli Osborn, 1903
Diplostomulum scheuringi Hughes, 1929
Diplostomulum sp.
Gyrodactyloidae
Macroderoides typicus (Winfield, 1929)
Neascus sp.
Octomacrum lanceatum Mueller, 1934
Paramphistomum stunkardi Holl, 1929
Phyllodistomum sp.
Phyllodistomum staffordi Pearse, 1924
Posthodiplostomum minimum (MacCallum, 1921)
Tetracotyle sp.
Triganodistomum attenuatum Mueller and Van Cleave, 1932
Triganodistomum sp.
Uvulifer ambloplitis (Hughes, 1927)
Cestoda
Abothrium crassum (Bloch, 1779)
Bothriocephalus claviceps (Goeze, 1782)
Bothriocephalus cuspidatus Cooper, 1917
Bothriocephalus sp.
Examined 2
Infected 2
Acanthocephala
Abothrium crassum
Azygia angusticauda
* Diplostomulum sp.
Haplonema hamulatum
Hepaticola bakeri
Leptorhynchoides thecatus
Trout
1
1
l3
11
l3
12
l1
l1
Check List of Parasites
Trematoda
Alloglossidium corti (Lamont, 1921)
Alloglossidium geminus (Mueller, 1930)
Bang ham — Parasites of Northern Wisconsin Fish 323
Cestoda (continued)
Corallobothrium fimbriatum Essex, 1928
Glaridacris catostomi Cooper, 1920
Proteocephalus ambloplitis (Leidy, 1887)
Proteocephalus fluviatilis Bangham, 1925
Proteocephalus laruei Faust, 1919
Proteocephalus pearsei La Hue, 1919
Proteocephalus perplexus La Rue, 1911
Proteocephalus pinguis La Rue, 1911
Proteocephalus sp.
Proteocephalus stizostethi Hunter and Bangham, 1933
Triaenophorus nodulosus (Pallas, 1781)
Nematoda
Agamonema sp.
Camallanus sp.
Capillaria catenate Van Cleave and Mueller, 1932
Contracaecum brachyurum (Ward and Magath, 1917)
Contracaecum sp.
Dichelyne cotylophora (Ward and Magath, 1917)
Dichelyne robusta (Van Cleave and Mueller, 1932)
Haplonema immutatum Ward and Magath, 1917
Haplonema hamulatum Moulton, 1931
Haplonema sp.
Hcpaticola bakeri Mueller and Van Cleave, 1932
Philometra cylindraca (Ward and Magath, 1917)
Philometra nodulosa Thomas, 1928
Philometra sp.
Rhabdochonia sp.
Spinitectus carolini Holl, 1928
Spinitectus gracilis Ward and Magath, 1917
Spinitectus sp.
Spiroocys sp.
Acanthocephala
Leptorhynchoides thecatus (Linton, 1891)
N eoechinorhynchus crassus Van Cleave, 1919
Neochinorhynchus cylindratus (Van Cleave, 1913)
N eoechinorhynchus sp.
N eoechinorhynchus tenellus (Van Cleave, 1913)
Octospinifer macilentus Van Cleave, 1919
Pomphorhynchus bulbocolli Linkins (in Van Cleave, 1919)
COPEPODA
Achtheres micropteri Wright, 1882
Argulus catostomi Dana and Herrick, 1837
Ergasilus caeruleus Wilson, 1911
Ergasilus elegans Wilson, 1914
324 Wisconsin Academy of Sciences, Arts and Letters
Copepgda (continued)
Ergasilus sp.
Ergasilus versicolor Wilson, 1911
Protozoa
Ichthyophthirius multifiliis Fouquet, 1876
Lymphocystis johnstonei Woodcock, 1904
Myxobolns sp.
Scyphidia micropteri Surber, 1940
Trichodina renicola Mueller, 1932
Trichodina sp.
Mollusca
Glochidia
Hirudinea
I llinobdella moorei Meyer, 1940
Illinobdella sp.
Literature Cited
Bangham, R. V.
1940. Parasites of fresh-water fish of Southern Florida. Proc. Fla.
Acad. Sci., 5:289-307.
1940. Parasites of fish of Algonquin Park lakes. Trans. Am. Fish Soc.,
70:161-171.
1941. Parasites from fish of Buckeye Lake, Ohio. Ohio Jour. Sci.,
41:441-448.
Bangham, R. V. and Hunter, G. W., Ill
1939. Studies on fish parasites of Lake Erie. Distribution studies.
Zoologica. 24: 385-448.
Bangham, R. V. and Venard, C. E.
1942. Studies on parasites of Reelfoot Lake fish. IV. Distribution
studies and checklist. Tenn. Acad. Sci., 17:22-38.
Cross, S. X.
1933. Some host parasite relationships of the Trout Lake region of
Northern Wisconsin. Jour. Parasitol., 20:132.
1934. A probable case of non-specific immunity between two para¬
sites of ciscoes of the Trout Lake region of northern Wisconsin.
Ibid., 20:244.
1935. The effect of parasitism on growth of perch in the Trout Lake
region. Ibid., 21:267-273.
1938. A study of the fish parasite relationships in the Trout Lake
region of Wisconsin. Trans. Wis. Acad. Sci., 31: 439-456.
Hunter, G. W. Ill and Rankin, J. S.
1940. Parasites of northern pike and pickerel. Trans. Am. Fish. Soc.,
69: 268-272.
Miller, M. J.
1936. Bunoderina eucaliae gen. et sp. nov., A new papilose Allocreadi-
idae from the Stickelback. Canad. Jour. Res., 14:11-14.
Bangham — Parasites of Northern Wisconsin Fish 325
Mueller, J. F.
1931. A new species of Cyclochaeta from the uterus and urinary
bladder of Esox reticulatus (Abstract) Jour, of Parasitol. 18:126.
1932. Trichodina renicola (Mueller, 1931), a ciliate parasite of the
urinary tract of Esox niger. Roosevelt Wild Life Annals 3(2):
139-154.
1934. Additional notes on parasites of Oneida Lake fishes, including
descriptions of new species. Ibid., 3:335-373.
Mueller, J. F. and Van Cleave, H. J.
1932. Parasites of Oneida Lake fishes Part 2. Descriptions of new
species and some general taxonomic considerations especially
concerning the trematoda family Heterophyidae. Ibid., 3: 77-137.
Pearse, A. S.
1924. Observation on parasitic worms from Wisconsin fishes. Trans.
Wis. Acad. Sci., 21:147-160.
1924. The parasites of lake fishes. Ibid., 21:161-194.
SYRPHID FLIES OF THE GENUS CHEILOSIA , SUBGENUS
CHILOMYIA IN NORTH AMERICA (PART II)*
C. L. Fluke
University of Wisconsin
F. M. Hull
University of Mississippi
This subgenus was erected by Shannon (Ins. Insc, Menst.,
10: 121) to separate out those hairy-eyed species that have pile
on the slopes of the face in addition to that on the facial strips.
The antennal pits are separated by a distinct chitinized projec¬
tion. Sometimes the pile of the face is not so conspicuous on the
female, and may be entirely absent, as happens in Cheilosia
hirsuta Hull and Fluke and apparently in Cheilosia nigrovittata
Lov. These two species are very closely related and hirsuta may
be only a variety. For this reason these two are included in the
key to the species of Chilomyia. Other members of the genus are
readily placed in this group, as far as we have observed. C. occi-
dentalis Will, has been selected by Shannon as type of the sub¬
genus.
Most of the species of Chilomyia occur in Western North
America, only two so far being found along the Eastern sections
of North America, namely: primoveris Shannon and pontiaca
Shannon. In the higher altitudes of the Rockies they are quite
common in midsummer. Since a few species are known to be of
economic importance, a careful study of the group is necessary.
They are difficult to determine but due to the relatively few
species in this subgenus no particular trouble should arise in
making determinations.
Both sexes are not always known and since the two differ so
materially it will be a long time before all synonomy is cleared
up. Collections of large series at the same time and place will
help to associate the sexes. Even then difficulties may arise.
When Lovett described his species chintimini he did not recog-
* Goffe, 1944, Ent. Mont. Mag. 80: 238. This important paper on generic synonomy was
received after the manuscript was submitted for publication.
327
328
Wisconsin Academy of Sciences, Arts and Letters
Explanation of Figures
All drawings were made with the aid of the camera lucida. Basal seg¬
ment omitted on the antennal drawings.
Fig. 1 — Chilomyia variseta, n. sp., profile of head of female with lines added
to show tubercle angles.
Fig. 2 — Chilomyia hoodiana Bigot, antenna of male.
Fig. 3 — Chilomyia hoodiana Bigot, profile of head of female.
Fig. 4 — Chilomyia yukonensis Shannon, profile of head of male.
Fig. 5 — Chilomyia variseta, n. sp., profile of head of male.
Fig. 6 — Chilomyia varipila, n. sp., profile of head of male.
Fig. 7 — Chilomyia pontiaca Shannon, profile of head of female.
Fig. 8 — Chilomyia burkei Shannon, profile of head of female.
Fig. 9 — Chilomyia burkei Shannon, antenna of male.
Fig. 10 — Chilomyia chintimini Lovett, profile of head of male.
Fig. 11 — Chilomyia fuma, n. sp. profile of head of female.
Fig. 12 — Chilomyia primoveris Shannon, antenna of female.
Fig. 13 — Chilomyia primoveris Shannon, profile of head of male.
Fig. 14 — Chilomyia coerulea, n. sp., profile of head of female.
Fig. 15 — Chilomyia coerulea, n. sp., antenna of female.
Fig. 16 — Chilomyia livida Wehr, profile of head of male.
Fig. 17 — Chilomyia occidentals Williston, profile of head of male.
Fluke and Hull — Syrphid Flies in North America ( Part II) 329
330 Wisconsin Academy of Sciences , Arts and Letters
nize the female, as a subsequent study of his material shows,
even though he had it before him at the time.
It has always been difficult to describe the facial tubercle,
whether prominent or low, and the amount of the excavation
above. Figure 1 has been drawn with lines to help in determin¬
ing the angles made by the various shapes of the tubercle. It
should be remembered that the two sexes often differ in the
prominence of the tubercle but the general trends can be indi¬
cated by this method.
Those who have been of special aid in these studies were
mentioned in Part I but for this Part we wish especially to thank
Dr. H. A. Scullen of Oregon State College and Dr. C. H. Curran
of the American Museum.
Table of Species — Males
1. Dorsum of thorax entirely covered with dark brown or black pile, rarely
a few pale hairs along the anterior margin . 2
Dorsum of thorax with at least some pale, whitish brassy, or silvery pile
visible, sometimes mixed with black or brown pile . 3
2. Thorax anteriorly with two obscure gray vittae, visible from behind
(Western) . hoodiana Big.
Thorax non-vittate . 7
3. Thorax with a distinct band of black pile (Oregon) .
. Cheilosia nigrovittata Lov.
Thorax not banded, though the black pile may be concentrated just
before the scutellum . 4
4. Thick white pilose species . .5
At least considerable black pile upon mesonotum or abdomen or hind
legs; often predominantly brassy pilose . 6
5. Scutellum with black bristles on the margin, pile of front black (Cali¬
fornia) . pacifica Hunt.
Scutellum covered entirely with silky yellowish white pile, pile of front
white (Colorado) . livida Wehr.
6. Legs black, the bases of the tibia sometimes very dark brown (Alaska)
. yukonensis Shan.
Legs with the bases of the tibia and their apices and the tarsi light in
color or yellowish-red to reddish . 11
7. Pile along the lateral margins of the abdomen everywhere dense and long,
black in color; sometimes with yellowish hair in the basal corners of the
tergites . 8
Pile of those areas chiefly pale; sometimes with a few black hairs on the
margin of the fourth tergite and all black on the margins of the second
tergite . 9
8. Downward projecting pile below the rim of the scutellum yellow in color,
halteres brown (Oregon) . chintimini Lov.
This pile black, halteres yellow (Washington) . burkei Shan.
Fluke and Hull — Syrphid Flies in North America ( Part II) 331
9. Fourth tergite with thick, long, pale yellow pile; only the central part
with black pile; thorax red-brown pollinose viewed from in front, a little
pale pile mixed with the black along the anterior and posterior margins
(Western) . . . variseta n. sp.
Pile of the fourth tergite less dense, black in the middle and on the
apical corners . . . ....10
10. Pile on the scutellum white and black mixed, tip of arista black - ....
. . . . . . . yukonensis Shan.
Pile of the disk of the scutellum wholly black, tip of arista yellow (Alber¬
ta) . varipila n. sp.
11. Rather large flies; the facial strips wide, densely pale pubescent, pale
pilose; facial pile pale with some black hairs intermixed; sometimes
largely black pilose, lighter areas of legs tending usually towards brown,
stigma and veins brownish; apical and hypopygial pile black: pile of basal
ventral half of hind femora golden (California) . . occidentalis Will.
Medium sized flies, the facial strips narrow, sparsely pubescent, apparently
bare; facial pile chiefly pale; lighter areas of legs tending towards pale
orange; stigma and the veins largely yellow; terminal pile of abdomen
golden; femoral ventral pile black almost to base . 12
12. Mesonotum almost wholly pale yellow pilose including area before scutel¬
lum and disc of scutellum; middle and hind tarsi light yellow; abdominal
pile pale yellow, antennae light brown to orange; wing base pale yellow
brown (Maryland) . primoveris Shan.
Mesonotum with some black pile mixed all over, especially before the
scutellum, some on scutellar disc; antennae dark brown; wing base smoky
(Western) . Cheilosia hirsuta Hull and Fluke
Table of Species— Females
1. Thorax with gray vittae upon the anterior half, seen from behind, third
antennal segment bright orange . . . . . . . 2
Thorax non-vittate . . . . . . 6
2. Pile of mesonotum mostly pale yellow or whitish; greenish black flies
(Oregon) . . . . . hoodiuna Big.
Pile of mesonotum black . . . 3
3. Peep, shining blue in color, abdomen more robust, thoracic vittae ob¬
scure . . . . . 4
Shining bluish-black, pile of face white and black, abdomen more elon¬
gate; vittae median and distinct; thoracic pile quite appressed. wholly
black except for pleura and sides of notopleura ; subapical cross vein quite
arcuate; third antennal segment bright orange (New Mexico) . . .
. . . . . . . . . . sonoriana Shan.
4. Scutellar discal pile mostly white (Washington) . . coerulea n. sp.
Scutellar pile all black or nearly so . . 5
5. Tibiae yellowish at base, antennae orange, wing veins yellow (New
Hampshire) . . . pontiaca Shan.
Legs darker, antennae darker, wing veins brownish yellow (Washington)
. . . .burkei Shan.
6. Pile of thorax quite flat, extremely appressed . . . . . 7
332 Wisconsin Academy of Sciences, Arts and Letters
7.
8.
9.
10.
ll.
12.
13.
14.
15.
16.
17.
Pile of thorax erect or suberect, not obviously appressed . 10
Scutellum with black bristles on margin . 8
Scutellum without bristles, or if present, they are pale yellow in color . .9
Scutellar bristles quite short (Washington) . variseta n. sp.
Scutellar bristles long and slender (California) . . pacifica Hunt.
Third antennal segment wholly brownish black; front with at least as
much black pile as pale pile; mesonotal pile quite short, brassy, black in
the middle. Scutellar margin with a few quite short golden bristles
(Washington) . . . variseta n. sp.
Third antennal segment reddish-brown, especially below, often rather
light, its dorsal margin always blackish. Scutellar margin without any
trace of short bristles (Alaska) . yukonensis Shan.
Pile of hind tibia partly or wholly black, at least on outside . 11
Pile of hind tibia wholly pale . 14
Small, blue -black species; third antennal segment bright orange; facial,
frontal, mesonotal pile black (Eastern) . pontiaca Shan.
Usually larger; black aeneous or greenish-black species; this pile in part
pale; third antennal segment dark brown or black on dorsal third or
less . 12
Scutellar margin with pale bristle like hairs (Alberta) . varipila n. sp.
Scutellar margin with strong black bristles . 13
Front swollen, pile of thorax mostly pale in color, rather short; small to
medium sized species (Oregon) . fuma n. sp.
Large, quite robust greenish or brassy-black flies, the front not swollen;
front with a conspicuous shallow transverse impression in the lower por¬
tion; pile of thorax golden, with longer, fine black erect hairs intermixed
(Oregon) . chintimini Lov.
Scutellar bristles conspicuously differentiated from the golden discal pile,
black in color; rather large, brassy-black flies . 15
Scutellar bristles not well differentiated . 16
Pile of front and mesonotum yellowish, usually a few black hairs inter¬
mixed (California) . occidentalis Will.
Pile of front white, of mesonotum short and white, pile of abdomen
white, short, dense and appressed except along the sides (California) ....
. pacifica Hunt.
Pile of greater and terminal part of abdomen erect; all pile everywhere
light yellow to brassy; small flies, the tibia and tarsi and wing veins
extensively light orange; one or two black notopleural bristles . 17
Pile of fourth segment flattened posteriorly; pile white; larger flies, the
tibia and tarsi less conspicuously orange; wing veins brown, no black
notopleural bristles (Colorado) . . . livida Wehr.
Tubercle of face distinct, but broad and low in profile. Front flattened and
microrugulose (Maryland) . primoveris Shan.
Tubercle small and short, (abrupt above and below) front trisulcate ....
. . . . . primoveris var.
Fluke and Hidl — Syrphid Flies in North America (Part II) 333
Cheilosia (Chilomyia) lioodiana (Bigot)
Figures 2 and 3
Cartosyrphus hoodiana Bigot, 1883, Ann. Soc. Ent. France, No.
32, part 23, p. 552.
Chilosia petulca Williston, 1886, Bui. U. S. Natl. Mus. No. 31,
p. 39.
Chilosia hoodiensis Williston, Ibid., p. 292.
Chilosia hoodiana Shannon, 1922, Ins. Insc. Menst., 10 : 131, 138.
A dark species with a pair of gray almost white pollinose
vittae on the anterior half of the mesonotum, best seen from
behind. Antennae of the male rather dark, somewhat reddish
brown below, of the female characteristically yellowish. Pile of
the mesonotum on the male black and erect ; on the female partly
appressed, mostly pale except for a setigerous black patch just
above the wing base. Scutellum of the female with strong black
bristles. Length 9 to 10 mm.
Distribution : Oregon (Type in Brit. Mus.)
Material reviewed: Idaho — Craig Mts. 1 male July 8, 1918
(Melander) ; Moscow Mt. 3 females July 4-5, 1919 (Melander),
2 females July 10, 1920 (Shannon). Oregon — Ashland, Bead
Indian Road 2 females July 19, 1943 (Scullen) ; Corvallis 1 male
April 6, 1936 (Rieder) ; Mt. Hood 1 male July 29, 1921
(Downes), 2 females July 18, 1933 (Wilcox). Washington —
Mt. Rainier 1 female July 14, 1914 (Fox), 1 male and 7 females
July 7, 1926, 1 female July 17, 1926 (Darlington), 2 females
August 14, 1932 (Baker), 1 male and 1 female July 25, 1936
(Baker) ; Paradise Inn 5 females July 19, 1931.
Records of others: British Columbia, Colorado, New Hamp¬
shire (error), New Mexico and Wisconsin.
Cheilosia (Chilomyia) sonoriana Shannon
Chilosia sonoriana Shannon, 1922, Ins. Insc. Menst., 10 : 136.
A shining blue black species; pile of the face short, white
below the tubercle, black next to the facial strips; tubercle
prominent; antennae nearly round, bright orange (female).
Mesonotum with short appressed black pile which is longer on
the sides, a small tuft of black pile on the upper edge of the
mesopleura; disc of the mesonotum with a pair of white vittae
on the anterior half ; in this respect quite similar to hoodiana.
Scutellum with strong black bristles on the rim, pile on the disc
white.
334 Wisconsin Academy of Sciences , Arts and Letters
Distribution : New Mexico (Type, a female in the U. S. Na¬
tional Museum).
Material reviewed : A single female from Moscow Mountains
Idaho (Hull Collection).
This specimen agrees in all essential details with the type
except for the more whitish squamae and somewhat paler hal-
teres.
Cheilosia ( Chilomyia ) yukonensis Shan.
Figure 4
Chilosia yukonensis Shannon, 1922, Ins. Insc. Menst., 10: 129.
Dark aeneous species with black and white pile. Scut ell um
with no prominent, strong bristles. Length 10 to 11 mm.
Male : — Face shining, lightly pubescent, more heavily so be¬
low the antennae and along the facial strips. The pile on the
sides of the face black, on the cheeks and facial strips white.
Front somewhat inflated with a deep sulcus, pubescence white
and confined mostly to the ocular border ; the pile all black, the
arch above the antennae shining orange colored. Antennae dark
orange, first two segments almost brownish and the upper third
of the third segment brown, sometimes nearly all brown; the
arista brownish and pubescent. The ocellar tringle shiny black
with long, black pile; the occiput shiny, white pubescence on
lower half next to the eyes; the upper cilia black with a few
white hairs near the vertex; pile on the lower half white. Pile
of the eyes moderately heavy, whitish below becoming light
brown above.
Thorax : — Mostly shiny, somewhat dulled on the disc of the
mesonotum. Pile of the mesonotum is black and white mixed,
mostly black on the notopleura ; pile of the pleura mostly whitish
with black hairs on the upper edges of the mesopleura and the
pteropleura. Scutellum shiny with long yellow and black hairs
on the discs and margins, shorter white hairs intermixed; the
ventral fringe long and white. Legs dark brown, somewhat red¬
dish brown on the tibiae ; pile mostly black, a few v/hite hairs at
the base and outer sides of the femora; there are some excep¬
tionally long hairs both black and white on the outer surfaces
of the femora. Wings hyaline with light brownish tinge, the
veins dark brown, stigma yellowish. Squamae whitish with yel¬
lowish border; plumule yellowish; halteres dark brown, the
stalks light brown.
Fluke and Hull — Syrphid Flies in North America ( Part II) 335
Abdomen Shining aeneous, opaque on the discs of the sec¬
ond and third tergites; the pile is mostly yellowish white and
erect, except on the discs where they are partly black and flat.
There are two or three black hairs on the anterior corners of the
second tergite. Ventral hairs white.
Female : — Mostly shining; hairs on the lower half of the
front mostly pale, almost whitish ; on the upper half of the front
the white hairs are intermixed writh black hairs, becoming all
black around the ocelli. Just above the arch is a flat, shiny,
slightly depressed area; there is also a shallow depression on
the sides near the eye borders ; on each side of the front a sulcus.
The pile of the face is shorter and practically all white. Pile of
mesonotum appressed and nearly all black, whitish along the
sides. Pile of scutellum whitish sometimes with a few longer
black hairs on the sides near the edge. There are about three or
four black bristles on the postalar callosities, one on the noto-
pleura, and four or five short ones just above the wing base.
Legs lighter in color at the knees, the pile much shorter and
paler in color. Pile of the abdomen mostly appressed beyond the
second tergite.
Distribution : Type Alaska. This species was named by
Shannon but he gave no description and did not designate any
types but a recent letter from Washington states that he did
label a holotype.
Material reviewed: Alaska — Firth to Lat. 69, June 27, 1920
(Jessup). Colorado — -Cameron Pass, 10 males, 7 females, (10,-
500 feet), July 7, 1931; Pingree Park, 13 females (9,000 feet),
July 9, 1931; North Park, 1 male, 2 females, July 1, 1932; Cree-
de, 1 male, 6 females, June 24, 1926 (E. G. Anderson) ; West-
cliffe, 2 males, June 12, 1926 (E. G. Anderson) ; Sargent, 1 male,
June 24, 1929, (E. G. Anderson) ; Granite Peaks Camp, Bay-
field, 2 females, July, 1928, (Bequaert) ; Rainbow Lakes, Boulder
Co., 1 female June 15, 1936, (Rodeck) ; Long's Peak, 1 female,
June 19, 1922; Grand Mesa, 1 female, July 8, 1938, (Rodeck) ;
Lake City, 4 females, August 8-21, 1938, (Fluke). Alberta,
Can. — Nordegg 2 males June 10, 1921 (McDunnough) ; Water-
ton 4 females June 24, 1923 (Seamans). British Columbia —
Hedley 3 males and 1 female July 3, 1923 (Garrett) ; Kootapnic
Valley 1 female July 1, 1925 (MacDougall) ; Lilloet 1 female
July 1, 1924 (MacDougall), 1 male July 10, 1916 (Phair), 1 fe-
336 Wisconsin Academy of Sciences, Arts and Letters
male July 28, 1933 (McDunnough), 1 male July 12, 1926 (Buck-
ell) ; Mt. Lolo, Kamloops 1 male June 2, 1938 (Jacob) ; Revels-
lake Mt. (6000 ft.) 1 female August 12, 1923 (Vroom).
Cheilosia ( Chilomyia ) variseta n. sp.
Figures 1 and 5
Shining black, the mesonotum of the male with faint brown¬
ish vittae. Scutellum of the male with long black bristle-like
hairs on the margins ; on the female the bristles are very short
and nearly all black, occasionally a pale one. Length 10 to 11 mm.
Male: — Front, face and cheeks shining black, very lightly
whitish pollinose on the occular borders of the front, below the
antennae, below the tubercle, and on the cheeks. Facial pile
black, more whitish near the mouth and white on the cheeks;
facial strips with white pile. There is a prominent patch of
whitish pollen next to the eyes on the cheeks. Front shining with
black pile ; rather strongly inflated, but with a very deep median
sulcus. Ocellar triangle semi-shining black with black pile. Occi¬
put black and with black pubescence except very narrowly gray
next to the eyes below ; the pile all black above becoming yellow¬
ish on the lower third. Antennae dark reddish-brown, the arista
black with short pubescence. Eyes brownish pilose becoming
almost whitish on the lower half.
Thorax: — Mesonotum, scutellum and pleura shining black,
with three faint brownish vittae which are seen best from the
sides ; the pile all black with a few whitish hairs near the scutel¬
lum. Pile of the pleura black, a few yellowish hairs on the ster-
nopleura, and all white just above the front coxae. Pile of the
scutellum rather long and mostly black with a few white hairs
along the fore margin, the bristles of the edge not very strong ;
ventral fringe long and yellowish white.
Legs : — Dark reddish-brown to black, the tibiae slightly less
darkened than the femora ; the pile mostly black with the excep¬
tion of a few white hairs at the base and outer sides of the
femora, a few at the base of the coxae and golden on the under¬
sides of the posterior metatarsi. Wings translucent, slightly yel¬
lowish on the anterior half, stigma yellow; squamae yellowish,
the fringe long and yellow on the lower lobe, shorter and black
on the upper lobe ; plumule light brown ; the halteres dark brown.
Abdomen : — Shining, very broadly opaque on the discs of the
Fluke and Hull — Syrphid Flies in North America ( Part 11) 337
first three tergites and rather expanding on the posterior border
of the second and third tergites. Pile entirely yellowish along
the sides, but flat and black on the opaque areas; a patch of
rather long black hairs at the basal corners of the first and sec¬
ond segments. Venter shining with pale pile.
Female: — Front shining aeneous, pile black with shorter
yellowish hairs intermixed; the usual depressed area above the
shining arch and along the sides next to the eyes ; pile of the face
white. The median sulcus practically absent although present
just below the median ocellus. Pile of the mesonotum flat, ap-
pressed and mostly all black, a few yellowish hairs both anter¬
iorly and posteriorly; short black bristles all along the sides.
Pile of the scutellum flattish, mostly yellow, but with short setous
hairs bordering the rim, which are all black ; the bristles on the
rim are short and usually black in color although on some speci¬
mens a pale bristle or two appears. Pile of the abdomen nearly
all appressed, more erect anteriorly and in the corners of the
segments, pale whitish along the sides, practically all black on
the opaque areas of the discs. The fringe of hairs on the upper
lobe of the squamae are yellow and the hal teres are often yellow¬
ish brown.
Types : — Holotype, male, Mt. Rainier, Wash., Sunrise, 6,318
ft., VII-24-1932, (J. Wilcox). Allotype, female (same date as
Holotype), collected VII-27-1932, (6,318 ft.). Paratypes, males :
one, Mt. Rainier, Wash., Sunrise, 6,380 ft., VIX-23-1932, (J. Wil¬
cox) ; one, Mt. Rainier, Wash., Sunrise, 6,400 ft., VII-29-1933,
(J. Wilcox) ; one, Mt. Rainier, Wash., Shadow Lake, 6,200 ft.,
VII-25-1932; one, Mt. Tallac, Tahoe, Calif., VII-19-1916, (E. P.
Van Duzee) . Females : two, Mt. Rainier, Wash., Sunrise, 6,380
ft., VII-27-1932, (J. Wilcox) ; one, Mt. Rainier, Wash., Sunrise,
6,380 ft., VII-31-1932, (S. E. Crumb) ; one, Mt. Rainier, Wash.,
Sunrise, 6,400 ft., VII-30-1933, (C. H. Martin) ; one, Mt. Rainier,
Wash., Tipsoo Lake, 5,400 ft., VII-30-1927, (M. C. Lane) ; one,
Toppenish, Wash., V-10-1927, (M. C. Lane) ; one, Mt. Rainier,
VII-7-1926 ; two, Grand Mesa, Colo., VXI-8-1928, (Lanham), VII-
10-1938, (Bauer) ; Holotype in the American Museum.
There is considerable variation in the females, especially as
to the amount and length of the bristles on the scutellum and the
amount of black pile on the front. The antennae of the Colorado
specimens are also more orange. The males, however, are fairly
338 Wisconsin Academy of Sciences , Arts and Letters
homogeneous, while the amount of brown pollen on the meson -
otum constitutes the principal variable.
It is possible that this species will grade into yukonensis
which according to our understanding of the female does not
have black bristles on the rim of the scutellum. It is possible that
specimens from Alaska may be found that will come within the
scope of variseta. The males of the two species appear to be
quite uniformly distinct.
Cheilosia ( Chilomyia ) varipila n. sp.
Figure 6
Similar to variseta ; the mesonotum of the male less densely
brown poliinose and the pile is more generally black especially
on the mesonotum, scutellum, and fourth abdominal tergite. The
female is more readily separated on the erect pile of the meson¬
otum and all pale bristles on the scutellum. Tips of the aristae
of both sexes yellow. Length 9 to 9.5 mm.
Male : — Head shining reddish-brown to black, a reddish spot
on the lower oral angles and almost yellowish on the cheeks. Pile
on the front, face, ocellar triangle, lower strips, and occiput
black; on the cheeks, upper four-fifths of the facial strips, and
eyes yellow. Pubescence very sparse, heavier on the strips, in
the corners by the antennae, and very narrowly next to the eyes
on the occiput. Antennae dark brown, the first two segment^
shining black; the aristae brown, pubescent, the extreme tips
yellow.
Thorax : — Shining black, dorsum of the mesonotum lightly
brownish poliinose on the disc; pile all dark brown to black;
scutellar pile all black, the marginal hairs longer and stouter;
downward hanging hairs yellow. Legs dark brown to black, the
pile all black except for a few yellow hairs on the femora and
the usual cushion of yellow hairs on the underside of the hind
tibiae and tarsi. Wings tinged with yellow, the stigma light
brown, the veins brown. Squamae yellow, lower fringe yellow,
upper shorter and black. Plumule yellow, halteres black.
Abdomen : — Shining black, dulled on the discs of the second
and third tergites ; pile yellow along the sides but nearly all
black on the sides of the first and second tergites and posterior
corners of the fourth tergite; black and yellow down the middle
of the abdomen; pile black on the genetalia. Venter shining with
yellow pile.
Fluke and Hull — Syrphid Flies in North America ( Part II) 339
Female : — Facial pile white ; frontal pile black with numer¬
ous shorter yellow hairs; antennae larger and partly orange.
Menonotal pile shaggy, almost erect, covered with longer black
and shorter yellow hairs; pile of the pleura pale, a patch of
bristle-like hairs on the upper edges of the mesoplura and ptero-
pleura; pile of the scutellum appressed, all yellow including the
short bristle-like hairs on the margin. Squamae white with yel¬
low fringe, halteres yellow. Abdominal pile closely appressed
beyond the second tergite, white to yellow along the sides, black
down the middle.
Types : — Holotype, male and allotype, female, Laggan, Al¬
berta, Lake Agnes, 6,800 feet, July 10, 1925 (0. Bryant), (Hull
collection). Paratype Male , Waterton Lakes, Alberta, June 24,
1923 (J. McDunnough) in Can. Nat. Mus.
This species is closely related to both yukonensis and vari-
seta but may be told from both of these by the yellow tips on the
aristae, more pronounced on the female.
Cheilosia ( Chilomyia ) chintimini Lovett
Figure 10
Chilosia chintimini Lovett, 1921, Proc. Calif. Acad. Sci., 11 : 277.
A large, generally shining black species; pile of the male
mostly black, of the female mostly yellowish brown ; legs black ;
rim of scutellum of female with black bristles. Length 10.6 to
12 mm.
Male: — Lovett did not mention the hairs on the face which
are numerous and black, otherwise his description is quite com¬
plete. Pile of the facial strips yellow. The arista is pubescent
almost to the end ; the squamae are whitish with golden fringe,
the plumule golden; some specimens are almost entirely black
pilose on the abdomen but others have patches of yellow pile on
the basal corners of the third and fourth tergites.
Female: — Quite similar to the male in body color but the
pile is yellow to golden on the face, cheeks, anterior corners of
the mesonotum, pleura, sides of the abdomen except the apical
corners of the third and following tergites, and generally on the
femora; the antennae are larger and orange except the upper
fourth which is brown ; front shining with a definite transverse
depression just above the antennae and a longitudinal sulcus on
each side ; mesonotal pile mostly black and all erect, a few black
340 Wisconsin Academy of Sciences , Arts and Letters
bristles on the notopleura, calli, and just above the wings ; 4 to 8
black bristles on the edge of the scutellum, pile on the disk
golden with a few longer black hairs, pile underneath golden;
about 4 or 5 black bristles on the upper edge of the mesoplura.
Tibiae paler basally. Halteres yellow. Pile on the discs of the
abdominal tergites black and appressed, becoming all black ex¬
cept the basal corners on the fourth tergite, otherwise yellowish
to golden.
Allotype, by present designation, female, Vernonia, Ore.,
April 13, 1936 on willow (K. Gray and J. Schuh).
Distribution : Oregon (Type in Calif. Acad. Sci. Coll.).
Material revieived: Oregon — Vernonia 9 males and 7 fe¬
males April 13-21, 1936, April 1, 1938, and April 17, 1937 (Gray
and Schuh) ; Astoria 1 female April 14, 1936 (Gray and Schuh) ;
Mary’s Peak 3 females April 19 (Lovett) and 1 female April 20.
1941 (Rieder).
Specimens from Vernonia were compared with the type and
we have also had the privilege of studying a paratype.
Cheilosia ( Chilomyia ) burkei Shannon
Figures 8 and 9
Chilosia burkei Shannon, 1922, Ins. Insc. Menst., 10: 141.
Chilosia a laskensis coquillett, (Not Hunter) 1905, Bur. Ent.
Cir. 61.
A dark blue species with black pile and orange antennae.
The facial strips are very narrow. This is one of the few species
in which the male has black pile on the underside of the scutel¬
lum.
Distribution : Washington (Type in U.S. Natl. Mus. Coll.)
Material reviewed: Colorado — Grand Mesa 1 female July 7,
1938 (R. Bauer) ; Snow Mass, Pitkin Co., 11,200 ft., 1 female
July 1, 1941, (F. M. Brown). Oregon — Florence 1 female April
14, 1931, (J. Wilcox). Washington — Dewatto 1 female June 7,
1906 (Aldrich). British Columbia — Vancouver 1 male May,
1913 (Hopping). Records by others: Moscow, Idaho.
This is the species reared from Western Hemlock and caus¬
ing a diseased condition called “Black Check.” The female may
be confused with pontiaca Shan, as there is very little general
difference between them, but burkei is darker; wing veins, an¬
tennae, legs. The male of pontiaca is as yet unknown.
Fluke and Hull — Syrphid Flies in North America (Part II) 341
Cheilosia (Chilomyia) pontiaca Shan.
Figure 7
Chilosia pontiaca Shannon 1922, Ins. Insc. Menst., 10 : 142.
Entirely like burkei Shan, except for paler wing veins, legs
and antennae. Shannon has compared the head widths and
heights but we are unable to note any differences. The geograph¬
ical range will separate the two. It is possible that these two
may prove to be the same. The male is unknown as the species
was described from three females taken on Mount Washington,
New Hampshire. Through the courtesy of the Museum of Com¬
parative Zoology we have had the privilege of studying one of
the paratypes.
Distribution: New Hampshire (Type female in Mus. of
Comp. Zool. Cambridge).
Material reviewed : New Hampshire paratype female. Que¬
bec, Laniel (F.Q.) 1 female June 11, 1937 (Atwood).
Cheilosia (Chilomyia) fuma n. sp.
Figure 11
A dark species with white erect pale pile on the mesonotum.
Frontal pile white below and black near the ocelli. Scutellar
bristles long and black. Abdominal pile mostly appressed, black
on the discs of the tergites, yellow along the sides. Length 9 mm.
Female. Head:— Eyes sparsely yellowish pilose; front
somewhat protuberant, rather wide, the sides not parallel, shin¬
ing brassy black ; there is on either side suboccularly a longitudi¬
nal furrow, quite shallow, which is roughened and in which the
pile seems to be somewhat thicker. There is a shallow pit before
the antennae. Pile of front on lower half wholly light yellow,
largely but not entirely fine and black upon the upper half and
between the ocelli. Behind the ocelli are several, quite long, fine,
black hairs and behind these the golden fringe of the occipital
pile consisting of sparse long hair and more abundant shorter
ones. Face black, highly shining; the tubercle small but promi¬
nent, deeply concave above ; the pile on the sides of the face rath¬
er sparse, pale brassy in color, the pubescence on the face lim¬
ited to the middle area on either side of the tubercle and between
the epistoma and the eyes. The facial strips are of moderate
width, apparently bare, their pile apparently consisting of a
single row of brassy hairs. Antennae of moderate size, almost
342 Wisconsin Academy of Sciences , Arts and Letters
orbicular, slightly pointed at the apex, the first segment black,
the second dark red, wholly pubescent and black pilose; the
third rather thickened, brownish red with the outer margin
blackish dorsally and apically. Arista short, dark brown, rather
strongly thickened on the basal third, noticeably pubescent.
Thorax : — Strongly shining brassy, the pile short, erect,
chiefly pale yellow. Over the middle of the mesonotum are a few
scattered fine black hairs and posteriorly a few longer ones. On
the notopleura, which is yellow pilose, is a single stiff black
bristle; there are two to three bristles above the wing and two
short ones and two much longer ones on the post calli. Pleura
pale brassy pilose, two black bristles on the upper part of the
mesopleura. Scutellum concolorous ; the erect discal pile brassy ;
there are two slender black bristles (pairs) on the margin, bas-
ally a single long pale one and some shorter pale ones.
Legs : — Dark brown, almost black, the femoral apices very
narrowly lighter brown. Tibiae likewise quite dark, their bases
indistinctly brown on approximately the basal third, but dark.
The apices of the tibia are also somewhat paler. All of the tarsi
are black or very dark brown, their dorsal pile is black. Pile of
the hind femora thick, abundant, golden on the basal and lateral
halves ; there are some long golden hairs reaching almost to the
apex of the dorsum, the short black setate hairs confined to the
ventral apical half. Pile of hind tibiae golden over the greater
part of the inner surface, becoming black dorsally and entirely
on the outer lateral surface.
Wings : — Somewhat obscured by poor preservation but uni¬
formly light brown, the base of the subcostal and marginal cells
paler, the stigma brown. Postical and subapical cross veins each
gently sinuous, each heavily spurred, the latter making a right
angle with the curvature of the third longitudinal vein.
Abdomen: — Long and slender but still much shorter than
the wings, shining brassy black, the pile pale golden, erect on
the sides of the second tergite, and in at least almost all of the
third tergite; elsewhere it is at least subappressed. There are
broad triangles located posteriorly in the middle of the second,
third and fourth tergites of flat appressed black pile. Pile of
fifth tergite almost wholly pale.
Holot-ype Female, Vernonia, Oregon; April 17, 1937, (on
willow) (K. Gray and J. Schuh), in the American Museum.
Fluke and Hull — Syrphid Flies in North America ( Part II) 343
The erect pile on the mesonotum relates this species to vari-
pila and livida , the bristles on the rim of the scutellum will help
to separate it.
Cheilosia ( Chilomyia ) coerulea n. sp.
Figures 14 and 15
A small shining aeneous species with four faint gray vittae
on the anterior half of the mesonotum. Pile of the front and
mesonotum black, appressed on the mesonotum. Antennae or¬
ange yellow with the narrow upper edge dark. Front very wide.
Length 6.5 mm.
Female. Head : — Eyes sparsely white pilose, the front
broad and not quite parallel, with a strong sharp impression
that does not quite reach the ocelli, through the middle of this
impression from eye to eye runs a shallow transverse depression.
On either side upon the end of the depression and adjacent to the
eye is a silvery pubescent semi-circular area which does not con¬
nect with the pubescence below the antennae. Color of front
black with a faint bluish cast, moderately shining, its pile almost
wholly black, erect and abundant. There is a little pale hair on
the lower part of the front; vertical and upper occipital hair
black. Face shining black with a bluish cast, highly polished,
the knob large, rounded but not conspicuous ; practically bare of
pubescence but with sparse white pile. Facial strips narrow,
pubescent, the pile white and apparently confined to a narrow
band of at most one or two hairs in width. Antennae of moderate
size, the first segment dark brown, the second light brown, the
third pale orange with a very narrow black dorsal border ; arista
black, thickened on the basal half, noticeably pubescent.
Thorax — Mesonotum polished shining blue black; viewed
posteriorly there are four gray pollinose vittae, the middle pair
dose together, shorter than the outer pair and pointed posteri¬
orly. Mesonotal pile quite short, subappressed, chiefly black;
some pale pile lies across the anterior margin. Notopleural pile
somewhat longer, black and pale, a few of the hairs longer and
stiffer. On the post calli there is both black and white pile and
one long bristle. Scutellum concolorous with short whitish pile
appressed towards the center; on the margin are two pairs of
long slender black bristles and three or four small short ones.
Legs Dark brown, shining, the apices quite narrowly light-
344 Wisconsin Academy of Sciences , Arts and Letters
er brown; the narrow base of the hind tibiae, basal two-fifths
of middle and anterior tibiae light brown ; all of the tarsi brown¬
ish-black, the middle basi tarsi lighter along the sides ; all dorsal
basi tarsal pile black. Pile of hind femora rather short, pale
along the sides except near the apex ; black pile ventrally limited
to the apical half ; pile of hind tibiae almost wholly black, both
inner and outer lateral surfaces largely silvery pubescent; hind
femora similarly silvery pubescent.
Wings: — Pale brown, the veins light brown, the stigma yel¬
low; the postical cross vein straight, the subapical cross vein
gently sinuous, both with strong spurs. The subapical cross vein
joins the third vein acutely with not over a 67 degree angle.
Abdomen: — Robust, a little wider than thorax; short, shin¬
ing bluish black; the pile exceedingly short, white except in the
center of the second and third tergites where along the pos¬
terior region are triangles of appressed short black pile. The
pile of the fourth tergite is much more sparse and, except on the
posterior margin, is nearly erect.
Holotype: — Female, Mt. Rainier, Washington, July 16, 1935,
White River Camp, (J. Wilcox), in the American Museum.
Cheilosia (Chilomyia) primoveris Shan.
Figures 12 and 13
Chilosia primoveris Shannon 1915. Proc. Ent. Soc. Wash., 17 :
168.
An Eastern Chilomyia which is easily distinguished from
pontiaca , the only other known species in the east, by its brassy
yellow pile on the mesonotum and abdomen. The antennae are
yellowish orange; the tibiae bicolored; pile on the front of the
male black, on the female yellow. Length 8 to 10 mm. The two
females from Utah are identical with the eastern specimens.
Distribution: Maryland (Type in U. S. Nat’l. Mus. Coll.)
Material reviewed : Maryland — Cabin John 1 male April 14,
1916 (Shannon). Massachusetts — Hyde Park 1 female May 6,
1905. New York — Paterson 1 female April 21, 1939 (Dietrich).
Ohio— Columbus 1 female May 9, 1925 (Painter). Utah — Lo¬
gan 1 female August 4, 1915; Salt Lake City 1 female. Vir¬
ginia — Fairfax Co. 4 females April 4 (Davidson) ; Great Falls
1 male April 15.
Fluke and Hull — Syrphid Flies in North America ( Part II) 345
Cheilosia ( Chilomyia ) occidentalis Williston
Figure 17
Chilosia occidentalis Williston, 1882, Proc. Amer. PhyL Soc. 20 :
305; 1886, Bull. U. S. Natl. Mus. No. 31, p. 41.
A dark aeneous species. Male with the pile of the mesonotum
long and mixed black and yellow ; the hairs of the face quite long
and black and yellow ; entire face rather conspicuously pollinose ;
pile of the scutellum very long and black on the apical margin
and almost bristle like, whiter at the base ; pile of the pleura all
yellowish, except for a large patch of black hairs on the meso-
pleura; the antennae dark brown to black. On the female the
mesonotal pile is mostly whitish and on the abdomen erect,
yellowish-white and appressed only on the discs of the segments ;
the scutellum with about eight bristles, some of which may be
pale and some black; the antennae are mostly orange-yellow,
darkened on the upper third.
Distribution : California (Type in U. S. Nat’l. Mus.).
Material reviewed : California — Berkeley 1 male and 2 fe¬
males July 6, 1904, 1 male August 24, 1915 (Van Duzee), 1 fe¬
male April 10, 1933 (Casier), 3 males March 12, 1936; San
Francisco 1 male March, 1893; Walnut Creek 7 males and 6
females March and April, 1936 (Davidson). Colorado — Grand
Mesa 2 males July 7, 1938 (Lanham).
Records by others : Alaska, British Columbia, New Hamp¬
shire (error), New Mexico and South Dakota.
Cheilosia {Chilomyia) livida Wehr.
Figure 16
Chilosia livida Wehr 1922, Univ. Studies, Lincoln, Nebr., 22 : 24.
A shining dark aeneous species with thick white to yellowish
pile; scutellum without bristles; antennae orange colored, with
the upper edge darkened, lighter on the female. Apparently re¬
lated to pacifica Hunter. Length about 9 mm.
Male. Head:— Face shiny, somewhat pubescent, the cen¬
tral knob bare, knob rather prominent and broad, semi-flat on
apex; the oral edge less prominent; lower sides of the mouth
devoid of pubescence and pile ; pile of front, face, and cheeks is
silky white. Front puffed with a medium sulcus, rather heavily
pubescent, the arch above the antennae shining black; facial
346 Wisconsin Academy of Sciences , Arts and Letters
strips very broad almost bare of pubescence except near the
eyes, the pile silky white. Antennae orange, the first two seg¬
ments and upper fourth of the third darker; arista dark in
color and very short pubescent, basal segment thickened. Ocel¬
lar triangle shiny with long white pile. Occiput gray pubescent,
the pile everywhere whitish. Eyes white pilose below, yellowish
above.
Thorax: — Everywhere shining aeneous, the pile everywhere
white and erect. Scutellum with long silky white pile, without
bristles. About four or five black bristles just above the wing
base. Legs shining black with yellow areas as follows : the
femora very briefly at the tips, the tibiae with their basal halves
and apical fifths, basal three segments of the four front tarsi;
the trochanters are somewhat reddish, especially on the fore
margins; pile mostly whitish, a few black hairs on the outer
apex of the hind femora and all black on the four hind tarsi. On
the outer edge of the tarsi are numerous small black bristles;
they are also quite prominent as a circlet at the tips of the four
hind tibiae. Wings hyaline, the veins yellowish to brownish,
stigma light yellow. Squamae white with light yellowish edge,
plumule yellowish white, halteres light brownish.
Abdomen : — Shining aeneous, opaque on the disc of the sec¬
ond and third tergites ; the pile whitish except broadly black on
the dorsum of the second, third and fourth tergites, pile erect
on the sides, flattened on the discs.
Female: — Very similar in all respects, antennae slightly
larger and more orange colored; front broad and shining; the
tiny bristles on the under side of the metatarsus of the middle
legs very strong; abdominal pile mostly erect, somewhat flat¬
tened on the discs of the segments both above and below.
Allotype: — By present designation, female, Lake City, Col¬
orado, Aug. 8 to 21, 1938, 9,000 ft. elevation (Fluke) ; in the
American Museum.
Distribution: Colorado (Type in IJniv. Nebraska).
Material revievjed: Colorado — Cameron Pass 1 male, 1 fe¬
male, July 7, 1931, Camp Creek R. Sta. 1 male June 19, 1920
(8700 ft.) ; Lake City 3 females August 8 to 21, 1938 (Fluke) ;
Powderhorn 1 female June 23, 1926 (Anderson) ; Snow Mass
Lake, Pitkin Co. 1 male July, 1941 (11,206 feet, Brown). Ore-
Fluke and Hull — Syrphid Flies in North America ( Part II) 347
GON — Corvallis 1 female April 12, 1936 (Ferguson). WASHING¬
TON — Roy 1 female April 29, 1932 (Latta) . Alberta — Medicine
Hat 1 male May 2, 1925 (Carr).
We have examined two of the male paratypes and our male
specimens are identical. The white pile of this species should
easily identify it. The lack of black bristles on the scutellum will
separate it from pacifica Hunter. It is much larger but more
slender than the eastern pale pilose species, primoveris .
C. livida var. lintea n. var. differs from typical livida in the
yellowish pile on the mesonotum. Holotype, male, Aspen, Colo.,
July 24-27, 1919 in the American Museum; paratype, male,
Boulder, Colo., May 29, 1922 in the Hull collection.
Cheilosia ( Ghilomyia ) pacifica Hunter
Chilosia pacifica Hunter, 1897, Can. Ent., 29 : 127.
Extensively white pilose, the scutellum with black marginal
bristles on both sexes. Front of the male black pilose, of the
female white.
We have been unable to recognize this species and also unable
to locate the types. They are not at the University of Nebraska
collection. It has been placed in the keys from the descriptions ;
the female in two sections as we are unable to determine wheth¬
er the mesonotal pile is erect or appressed. Hunter’s description
mentions the depressed pile on the abdomen which would indi¬
cate that the pile on the thorax is generally erect. If this is true
the female should be compared with occidentalis Will., otherwise
it appears to be related to livida Wehr, a species which does not
have black scutellar bristles. The females of pacifica and occi¬
dentalis may be difficult to separate but the pile of pacifica is
whitish and undoubtedly shorter than on occidentalis. The latter
species usually has a few black hairs intermixed in the heavy
yellow matt on the front ; described as short and white on paci¬
fica. The “short appressed pile” on the abdomen is not at all
characteristic of occidentalis.
Distribution : California (Types not located).
Material reviewed : None.
PRELIMINARY LIST OF THE HYDRACARINA
OF WISCONSIN
REVISION OF PART I
Ruth Marshall
Rockford College
Part I of the Preliminary List of the Hydracarina of Wis¬
consin (Marshall, 1931) listed, with brief descriptions and
drawings, 14 species of the so-called “red mites,” belonging to
seven genera then included in the Superfamily Limnocharae.
This group has now been subdivided and other superfamilies
recognized so that the genera have a new grouping as will be
noted. The classification of Viets (1936) is followed. Former
descriptions are supplemented with more drawings and notes,
synonymies indicated, and seven more species and varieties
added (new forms only in the Genus Eylais ), bringing the list to
21.
GENUS HYDRACHNA
The Hydrachnae are among the largest of the hydracarina
and are common in shallow waters throughout the world. They
are usually soft bodied, rotund, red or orange, with papillose
skin. Between the eyes lies the frontal organ whose function is
unknown. On the dorsal side there are developed chitinous struc¬
tures, usually paired, in a great variety of forms and sizes. The
epimera are in four groups which increase in size posteriorly.
The genital organ lies between the posterior groups of epimera ;
it has a pair of united plates, somewhat movable, and covered
with fine acetabula. The maxillary organ has a long, curved
rostrum at the end of which is the mouth. The mandibles are
awl shaped. The palpi are broadest at the base, the segments
decreasing in width distally. The legs have swimming hairs.
The genus is now placed with the small African genus Berg-
ena in a single family, Hydrachnidae , of the Superfamily Hy¬
drachnae. Five subgenera are recognized (Viets, 1936:58), dis¬
tinguished chiefly by the character of the dorsal structures, three
represented here by six species and one variety.
349
350 Wisconsin Academy of Sciences , Arts and Letters
Hydrachna canadensis Mar.
PL I, Fig. 1-4
The anterior dorsal chitin structures are represented by a
pair of irregularly shaped hair-bearing plates a short distance
behind each eye capsule; between each plate and the capsule is
also a small fleck of chitin. In epimera III there is a small spur¬
like process on the anterior inner side of each; in IV the inner
posterior margins are blunt, with thin subcutaneous processes.
In the palpi the proportions of the segments are shown in Fig. 4.
The genital organ is broadly heart-shaped in the female; the
male is unknown. The male described for this species (Marshall,
1929:63) is now recognized as another species, H. marshallae
(Lundblad, 1934:34). The nymph is now known; the anterior
dorsal structures resemble those of the adult and the epimera IV
are similar.
This species belongs to the Subgenus Rhabdohydrackna ,
characterized by a pair of chitin bars or small plates behind
each eye capsule. It has been found in Ontario, Manitoba and
Michigan as well as in Wisconsin.
Hydrachna miliaria Berl. (= H. bilunata Mar.)
PL I, Fig. 5-8
Behind each eye capsule is a small, somewhat lunate but
sometimes angular plate followed by a smaller, likewise variable,
rounded or elongated plate; these plates are alike in adult and
nymph. Characteristic of the epimera is the narrow prolonga¬
tion on the inner posterior margin of IV which is even more
pronounced in the nymph. In the palpi the 1st segment is large
and broad ; the 3rd is longer than the 2nd with a concave outline
on the inner proximal side.
The male is now known; the length is about 2.50 mm. The
genital organ is very large, fully one-third of its length extend¬
ing beyond the limits of epimera IV, the anterior margin with a
large indentation. Epimera IV have the characteristics of those
of the female but they are not as elongated, relatively broader,
the posterior inner prolongations shorter.
This species is believed to be the same as one described
earlier for South America (see Marshall, 1943b :404). It has
been found in British Columbia and appears to be widely dis¬
tributed throughout the United States.
Marshall — Preliminary List of the Hydracarina 351
Lundblad (1934:25) erected a new Subgenus T etrahydrach-
na, evidently designating this species as the type ; later the same
author (1941b :360) gave the new name as a synonym for Scuto -
hydrachna! Viets (1936:58) considers it a synonym for Rhabdo-
hydrachna .
Hydrachna cruenta Mull. (= H. schneideri americana Mar.)
PI. II, Fig. 13-17
This species is recognized by the very large dorsal shield
which has a projection extending forward between the eyes; the
posterior margin is wavy, more or less convex, the whole outline
subject to much variation. The length of the body is 2.00-3.00
mm. In epimera IV the posterior inner border is broadly ex¬
panded, especially in the female ; in the male the medial border
is longer, the entire plate shorter. The genital organ in the
female is very broad; in the male, elongated, hardly filling the
space between the posterior epimerai groups. The palpi are
rather slim; the characteristics of the segments are best shown
in Fig. 16. In the nymph there is a large elongated plate immedi¬
ately behind each eye capsule ; epimera show the characters of
the adult.
This is the type species of the Subgenus Hydrachna with the
large unpaired dorsal plate reaching the eye region and enclosing
the frontal organ. It is a cosmopolitan species and has been
found in widely separated areas in Canada and the United
States.
Hydrachna cruenta diminuata Lund.
PI. II, Fig. 18, 19
In the original description (Lundblad, 1934:10) based on the
study of one male (Connecticut), this variety has as its chief
character a diminished dorsal shield which does not have a pro¬
cess extending between the eyes ; nor does it enclose the anterior
hair plates ; also, the posterior outline of the shield is distinctly
concave. In the former description of the main species (Mar¬
shall, 1931:314), Fig. 22 should probably be referred to this
variety, although not conforming closely to Lundblad’s Fig. 4A.
A few specimens from Ontario as well as Wisconsin material
(Adams County) are also placed here. Both sexes were repre¬
sented and the female is now known (Fig. 19). However, in the
inclusion of the hair plates between the eyes in the dorsal plate
352 Wisconsin Academy of Sciences , Arts and Letters
they do not all conform to the original description but they do
show the posterior concavity. In view of the great degree of
variability in this respect in the species, the first description of
this variety may have to be revised.
Hydrachna magniscutata Mar.
PI. I, Fig. 9-12
This species resembles H. cruenta but is smaller (about 1.15
mm.), the large dorsal plate has but a slight projection between
the eyes, irregular in outline or concave ; in epimera IV the inner
posterior outline is rather short and blunt; the palpi are rela¬
tively stouter. In the nymph there are two obovate anterior
plates, well removed from the eyes.
It has been found in over twenty bodies of water in Wiscon¬
sin and across the United States from New England to Wash¬
ington as well as in Ontario and Alberta.
Mr. C. 0. Berg*, working at the Biological Station of the
University of Michigan at Douglas Lake, found several indi¬
viduals of this species in a pool at Sedge Point. Some of these
were blue, a feature already reported (Marshall, 1927:271).
Mr. Berg (unpublished correspondence) kept specimens in the
laboratory and observed the oviposition in Potamogetan richard-
soniiy many egg galleries being easily visible in the stem. The
emergence and development of the larvae were followed and
their attachment to Belostoma flumenium was seen.
Hydrachna crenulata Mar.
PL II, Fig. 20; PI. Ill, Fig. 24, 25
The body is almost circular, about 1.90 mm. long, deep red.
In the live specimen the anterior dorsal aspect shows two low
scallops between the eyes. The dorsal surface is entirely covered,
except in the eye region, by a finely porous chitinous plate which
extends over on the posterior ventral side ; this feature was un¬
fortunately overlooked in the original description (Marshall,
1930:247). In this plate are embedded two small irregularly
crescent-shaped chitin pieces directly below the eyes, down about
one-third of the body length ; near the usual gland openings with
accompanying hairs are flecks of chitin. Epimera IV show a pro-
* Publication of the complete record of these observations has been delayed. Unable to com¬
municate with Ensign Berg for permission, the author has taken the liberty of including here
this brief summary of his studies.
Marshall — Preliminary List of the Hydracarina 353
longed curved posterior inner outline. The male genital organ is
cordate and nearly fills the space between the last pair of epi-
mera. Below it lies the large inverted triangular area not cov¬
ered by the extension of the dorsal shield. The female is un¬
known. In the palpus is to be noted the considerable size of the
1st segment, the concavity on the inner border of the 2nd, the
position of the hairs (Fig. 20).
The species has been found in Wisconsin and Michigan.
This species belongs to the Subgenus Scutohydrachna (Viets,
1933:162) characterized by the development of a great unpaired
plate covering the dorsal surface and part of the ventral, H.
dorsoscutata of Brazil being described and designated as the
type species. Lundblad (1934:16) in his review of the author's
description of H. crenulata gave Viets' species as a synonym,
although noting the somewhat longer and slimmer inner pos¬
terior border in epimera IV, these processes of either side being
connected by a small strand of subcutaneous chitin. It should
also be noted that the male genital organ is shorter and broader
in the Brazilian form. Dr. Viets who examined the type speci¬
men of H. crenulata stated (unpublished correspondence) that
“H. dorsoscutata must be considered a variety of H. crenulata ”
differing only in the connecting chitinous line behind the genital
area. However, in a later paper (Viets, 1940:193) he again lists
it as a species. In the opinion of the present author it should
probably be considered a variety, certainly not a synonym for
H. crenulata.
Hydrachna rotunda Mar.
PI. II, Fig. 21-23; PI. Ill, Fig. 26
The body is almost circular, 1.10-1.12 mm. long, deep red.
Over the entire dorsal surface, except around the eyes, is de¬
veloped a finely porous chitinous plate which extends also over
on the ventral side to cover most of the surface outside of the
epimera, as in H. crenulata , but somewhat more extensively.
This character was unfortunately not given in the original de¬
scription of the species (Marshall, 1930:246). In this dorsal
shield behind each eye capsule is a small irregularly curved piece
of chitin together with gland openings and hairs very much as in
the related species. In epimera IV there is a slender prolonga¬
tion of the inner posterior border. The male genital organ is
very large, broader than long, almost filling the area between the
354 Wisconsin Academy of Sciences , Arts and Letters
posterior groups of epimera. The palpi are rather stout; the
proportions of the segments and the disposition of the hairs are
shown in Fig. 26.
The female is now known. The epimera are like those of the
male but somewhat longer, the last pair having a similar but
shorter prolongation of the medial posterior angle. The genital
organ is very large, much broader than long, the anterior lateral
border closely pressed upon epimera III and the anterior border
of IV.
This species, like the preceeding, belongs to the Subgenus
Scutohydrachna ; it has been found in Wisconsin, Illinois and
Tennessee.
GENUS LIMNOCHARES
Mites of this genus are large, red, soft bodied, papillose,
wrinkled, changeable in form. The circular mouth lies at the
end of a protruding rostrum. The eye capsules are close to¬
gether on a ligulate plate in the medial dorsal line. The epimera
are very small, in four groups, beset with long hairs: pair I,
somewhat rectangular, meet in the anterior medial corners; II
are triangular. The posterior groups are smaller, widely sep¬
arated, elongated. The genital orifice is small, without plates,
lying between the last pair of epimera and guarded by bristles ;
the sexes are much alike. The palpi are very small, especially
the 5th segment. The legs are short with many bristles ; in the
Subgenus Cyclothrix they have swimming hairs.
The Superfamily Limnocharae is now limited to three fami¬
lies of which Limnocharidae is one, with few species. The genus
Limnochares is represented in Wisconsin by two species.
Limnochares aquatica (L.)
PI. Ill, Fig. 27-29
Under this species was first included (Marshall, 1931:312)
all specimens of the genus ; it was soon apparent that two species
were present, of which L. aquatica was the less common. Lavers
(1941) made a study of available material and clarified the mat¬
ter. The body has a length up to 5.00 mm. ; it is somewhat shoul¬
dered, tapering to the snout-like rostrum. Epimera III and IV
are triangular. The legs are very short with many bristles but
no swimming hairs. These mites are slow moving, often crawl-
Marshall-Preliminary List of the Hydracarina 355
mg on the bottom of shallow waters. Lundblad (1941c: 155) uses
the older specific name, L. holosericea.
This species is one of the first water mites to be described.
It is widely distributed over Europe and now known for Siberia,
Japan, and South America. In North America it has been found
and reported in small numbers, sometimes in collections with
the next species, in Washington by Lavers; and in Michigan,
Indiana and Wisconsin (Vilas County) by the author where it
appears to be usually a bog form. Lavers (p. 3, 5) is in error
concerning certain previous records.
Limnochares americana Lund. (= L. natans Lav.)
PL III, Fig. 30-33
The body closely resembles that of L. aquatica ; it measures
up to 4 mm. in length. The ocular plates of the two species differ
in some details, being here wider. Epimera III are elongated,
while IV are boot-shaped. The legs, which are relatively slim,
have swimming hairs as well as long bristles on all legs; the
former are long and numerous on the middle segments of III
and IV. In consequence it is an active swimmer and the body is
very mobile. This places it in the Subgenus Cyclothrix.
The late C. H. Lavers made a detailed study of available
Limnochares material in American collections in connection with
his own material from the state of Washington. He wrote to
several hydracarinologists in Europe requesting identified speci¬
mens of L. aquatica for comparison. Dr. Viets responded with
several individuals from Germany. Lavers also studied the hab¬
its and development of his specimens. He gave the name L.
natans to the heretofore recognized but undescribed species. His
paper (1941), unfortunately delayed in printing, gave his prin¬
ciple findings ; some of his unpublished notes contain other ma¬
terial. In the meantime Dr. Lundblad secured a small collection
from Michigan and published a brief account, without drawings,
of what appears to be Lavers’ L. natans under the name L.
americana (Lundblad, 1941c: 155). Since this was published a
few months before the earlier and more complete paper, L.
natans must be considered a synonym.
L. americana is more common and widely distributed than
the older species. It has been found in British Columbia, On¬
tario, Washington, Colorado, Illinois, Michigan, Nebraska,
356 Wisconsin Academy of Sciences , Arts and Letters
Massachusetts, New Hampshire, New York; and in Wisconsin
in waters near Green Lake, Green Bay, Waupaca, Cable, in Storr
Lake and a pool near Lake Winnebago.
GENUS EYLAIS
Mites of this genus may attain a length of 5 mm. The skin is
soft, red, smooth or showing wavy lines. The two eyes of each
side are enclosed in a capsule; with rare exceptions the latter
are connected by a bridge of very variable outline. The maxil¬
lary organ encloses the circular, hair-fringed mouth. The epi-
mera are elongated and lie in the anterior half of the posterior
surface, pairs I and II of each side approximated, III and IV
joined only in the median line. The genital orifice lies between
the medial ends of the anterior epimera; the sexes are difficult
to distinguish. The palpi are slender with many bristles; the
4th segment is the longest, the 2nd and 3rd not completely chi-
tinized. Legs I-III have swimming hairs.
The genus is now placed, with the small genus Piersigiay in
the Family Eylaidae of the Superfamily Limnocharae. These
mites are common in quiet shallow waters of all continents.
Over 100 species have been described but many of these should
probably be regarded as varieties. Descriptions are based almost
entirely on the characters of the small ocular plate and this is
very variable. Four species and two varieties, three of them
new, have been determined for Wisconsin.
Eylais desecta Koen.
PI. IV, Fig. 39-41
In spite of some variation, the shape of the ocular capsules
and of the intercapsular bridge is fairly constant (Koenike,
1912:283). On the latter are two anterior rounded projections
each bearing a large bristle but they do not project beyond the
capsules; between and below them is a rounded process. The
bay below the bridge is deep and of varying width, reaching at
least as far as the middle of the capsules. A specimen reported
by the author from Winnipeg (Marshall, 1929 :62), then uniden¬
tified, is now referred to this species.
E. desecta is probably widely distributed, since it has been
identified in Ontario, Manitoba, North Carolina, Tennessee and
Michigan as well as several places in Wisconsin.
Marshall — Preliminary List of the Hydracarina 357
Eylais rimosa Piers.
PL IV, Fig. 48
This is a species closely resembling E. desecta, but the two
anterior projections on the short intercapsular bridge are more
pronounced with a deep incision between them, while the bay
posterior to the bridge is somewhat larger. It is “eine sehr
variable Form” (Viets, 1936:89) described under several names.
It has been found throughout Europe and North Africa, re¬
ported also from Siberia and India.
In Wisconsin a few specimens have been found in Fox and
Boulder Lakes.
Eylais infundibulifera bakeri n. var.
PL IV, Fig. 37, 38
The species E . infundibulifera Koen. is widely distributed
over Europe and reported also from Turkestan and Siberia;
several varieties are recognized. It is also known for Ontario.
The intercapsular bridge in the main species is short and
very broad with a large, more or less, irregular anterior central
projection and a shallow posterior bay. In the new variety,
E. bakeri , the bridge is longer so that the eye capsules are
farther separated, the anterior projection is shorter and more
irregular ; the posterior bay is deeper, the sides showing a more
or less conspicuous bulge midway on either side. The palpi are
rather stout ; the distal inner process on the 3rd segment is small
and only sparingly provided with short bristles. The body is
3.50-4.00 mm. long.
Specimens were found in Findley and South Turtle Lakes,
Vilas County, and in Lake Winnebago ; the latter collection was
made by Dr. F. C. Baker, for whom this variety is named.
Eylais gibberipons hirsutipalpis n. var.
PL IV, Fig. 42, 43
In Eylais gibberipons (Viets), of central Europe, and this
new variety the intercapsular bridge has an anterior-posterior
measurement about twice as great as the distance between the
eye capsules, an anterior projection with an indentation, while
the posterior bay is relatively small. The variety, E. hirsuti¬
palpis , conforms to this general plan of the ocular plate, but the
palpi differ from the stem species, the 4th segment being longer
and the 4th and 5th having many more short bristles.
358 Wisconsin Academy of Sciences, Arts and Letters
Only one specimen has been identified; this came from
Boulder Lake, Vilas County.
Eylais robusta n. sp.
PL IV, Fig. 44-46
The average length of the three specimens identified is about
3.00 mm. The eye capsules are broadly reniform. The inter-
capsular bridge is short, with a large rounded anterior process,
which may be somewhat irregular and indented (as in Fig. 45),
projecting beyond the capsules; between the attachment of the
two bristles is a large irregularly oblong surface. Posterior to
the bridge is a deep narrow bay, nearly the same width through¬
out, more than half the length of the capsules or contracted a
little by processes from the capsules. The palpi are long, espe¬
cially the 4th segment which bears but a few bristles; the 3rd
segment bears distally a small area of weak bristles on the con¬
cave side, with more and stouter bristles on the outside ; the 2nd
segment has a large bristle on the inner distal corner. In the
form of the intercapsular bridge with its anterior process the
new species resembles E. infundibulifera ; but the posterior bay
is much deeper and narrower.
The specimens came from Trout and Boulder Lakes.
Eylais falcata Koen.
PI. IV, Fig. 47
Characterized by Koenike (1912) as a species which “ap¬
pears to vary strikingly, particularly in the form of the eye
plate,” yet several individuals are here assigned to it on the basis
of the fairly constant and unusual features. The eye capsules
are very broad, oval or slightly reniform, sometimes broadest
anteriorly, the bases of the two large bristles on the capsules
rather than on the intercapsular bridge. The latter is short and
narrow, set well back from the anterior end of the capsules ; it
has an indentation on the anterior margin, the posterior side
more or less projecting. The palpi agree well with Koenike’s
Fig. 3.
The original material was found near Ottowa, Canada. In a
paper by the present author (Marshall, 1929:61) a specimen
from Manitoba (Fig. 17) was described but the name withheld;
it is now assigned to this species. In Wisconsin specimens have
been found near Green Lake and Madison.
Marshall — Preliminary List of the Hydracarina 359
GENUS CALONYX
This genus is a group of soft bodied, papillose red mites with¬
out chitin plates. The maxillary organ has a rostrum ; the palpi
are chelate. The epimera are in four groups, well separated, the
posterior in about the center of the under surface. The genital
orifice lies between the medial ends of epimera III, shorter in the
male, with slightly chitinized valves surrounded by numerous
stalked acetabula. The legs are short, without swimming hairs,
and end in scoop-shaped toothed claws.
This genus with the closely related Genus Protzia and four
other genera is now placed in the Family Protziidae in the Super¬
family Limnocharae ; they are bottom forms, more common in
alpine waters.
Calonyx ovata (Mar.) (= Protzia ovata)
PI. V, Fig. 59-62
The body is obovate ; largest specimens are 1.20 mm. long.
The large genital organ occupies most of the area between the
epimeral groups, the orifice in the male with a cluster of fine
hairs; it is surrounded by about thirty acetabula, irregularly
placed, the posterior with longer stalks.
This species has been found as an alpine form in California
(Marshall, 1943a :322) ; in Wisconsin it is known only for Green
Lake.
GENUS HYDRYPHANTES
The body of this genus is of moderate size, somewhat com¬
pressed dorsally, papillose and red. Between the eye capsules is
a chitinized plate in which lies the frontal organ. The maxillary
structure has a rostrum. The epimera are in three groups, the
last pair somewhat triangular. The genital organ has elongated
laterally hinged plates, each with three or more acetabula. The
palpi are cheliform. The legs are long, pairs II-IV with swim¬
ming hairs. The genus is very large, with many species, active
mites living in small bodies of shallow water in many parts of
the world.
The Superfamily Hydryphantae , Family Hydryphantidae , in¬
cludes this genus; under it are three subgenera, distinguished
chiefly by the number of genital acetabula. Specific descriptions
are based largely on the form of the dorsal plate; three species
have been found in Wisconsin.
360 Wisconsin Academy of Sciences , Arts and Letters
Hydryphantes ruber (de Geer)
PL V, Fig. 52, 53
The body may reach a length of 2.00 mm. in the female. The
dorsal plate is large, very variable in form but compact, the
anterior end convex, and wider than the posterior which ends in
two lateral prolongations. The palpi are stout. The genital
plates have each three acetabula characteristic of the Subgenus
Hydryphantes .
Viets (1939:75) questions the identity of the North Ameri¬
can specimens with Old World forms (Marshall, 1930:247;
1931:315), and states that the figures for the dorsal plate place
them nearer to H. planus Thon, and proposes H. novus nov. nom.
for them. In view of the great variability of the plate as shown
by various writers and the essential agreement of these speci¬
mens with them the author sees no justification for another
name.
The species is found throughout Europe where also several
varieties have been described, and in Kamtschatka; in Canada,
Ohio, Michigan, Illinois, Wyoming and in several localities in
Wisconsin.
Hydryphantes tenuabilis Mar.
PI. V, Fig. 49-51
The body is ovate, largest specimens about 1.00 mm. long,
the anterior slightly projecting. The dorsal plate is distinctive
and quite constant in form : an anterior piece between and above
the eye capsules with two diverging posterior limbs which bi¬
furcate to end in thin pieces. The epimera are heavy, the groups
close together, pair IV with a large median bulge on the posterior
border so that it lies close to the genital organ; the latter is
broader than in H. ruber , with three acetabula. Like the latter
species it belongs to the Subgenus Hydryphantes.
Daday (1905:279) described a new species from Paraguay,
H. ramosus , with a dorsal plate closely resembling that of H.
tenuabilis (Marshall, 1926:33). Lundblad (1938:7) described
another Paraguayan species, H. schadei (without figures) with
a similar dorsal plate, pointing out also differences in the palpi
between the new species and “der von Marshall abgebildeten
Form von H. ramosus” \ Later the same author (Lundblad,
1941a :56) made H. schadei a variety of H. ramosus (giving fig-
Marshall — Preliminary List of the Hydracarina 361
tires) and again referred to Marshall's finding of the latter
species omitting the name given by her, H . tenuabilis. In private
correspondence (1941) Lundblad stated that he regarded the
two species as identical. It is difficult to decide the matter from
Baday’s account; until the South American form can be studied
more fully the author will continue to use the present name.
It is possible that it should be regarded as a variety of the older
species.
This species has been found in several north-east central
states and in many waters in Wisconsin.
Hydryphantes multiporus Mar.
PL V, Fig. 54, 55
The body is about 1.50 mm. long, orange red. The dorsal
plate is large, the anterior part convex and reaching nearly to
the eye capsules ; it then narrows abruptly and passes over into
two long large pieces which taper and thin out, a large rounded
bay lying between them. The epimera are heavy, the groups
close together. The anterior end of the genital organ lies close
to the last epimera pair and is distinguished by the large number
of acetabula, 14 to 18, on the outer border of each plate, variable
in number even on the two sides. In the numph the number is
smaller, the plates shorter. The palpi are very stout, the first
three segments much shorter than broad on the concave side,
the 5th very short. The legs are stout, IV about the length of
the body; there are abundant bristles and numerous swimming
hairs.
The large number of genital acetabula places this species in
the Subgenus Polyhydryphantes. It has been found only in two
small bodies of water in Adams County.
GENUS DIPLODONTUS
The body in this genus is soft, papillose, red, with no dorsal
chitin plates nor frontal organ. The two eyes of each side are
separated, not enclosed in a capsule. The maxillary organ has a
rostrum and mouth disk. The epimera are in four groups. At
its anterior end the genital organ lies between epimera IV ; its
ovate plates bear many small acetabula. The palpi are slim,
chelate. The legs have swimming hairs.
This genus with the small African genus Oxopsis make up
the Family Diplodontidae of the Superfamily Hydryphaniae.
36 2 Wisconsin Academy of Sciences , Arts and Letters
Few species have been found but the one to be described is cos¬
mopolitan.
Diplodontus despiciens (Mull.)
PL V, Fig. 56-58
The body is nearly circular, compressed, reaching a length
of 2.00 mm., covered with small tapering papillae. The color is
deep red with a large dark central scalloped area. The epimera
are elongated, bordered with hairs, occupying a relatively small
part of the ventral surface ; pairs I and II are slightly attached
medially. The sexes are difficult to distinguish except for the
smaller size of the male. The palpi are small and slim; the 5th
segment with a similar process from the 4th form a long delicate
chela. The 1st and 2nd palpal segments have feathered bristles,
the 3rd, two long coarse bairs.
One of the first water mites to be described, this species is
perhaps the commonest of the water mites. It has been found
in all continents (except Australia?), in about half of the states
of the Union and in Wisconsin in practically all waters Where
collections have been made.
GENUS SPERCHONOPSIS
In this genus the skin is thick, papillose, with small paired
dorsal chitin plates and large wart-like elevations, likewise papil¬
lose, near the skin gland openings. The maxillary organ has a
slender rostrum. The epimera are in four groups, the last pair
somewhat triangular. The genital organ has lateral elongated
plates each with three acetabula on the inner margins. The
palpi have on the 2nd and 4th segments a large hair-bearing peg
on the concave side. The legs are without swimming hairs.
It is a small genus with one large species, next to be de¬
scribed. It belongs to the Family Sperchonidae , now placed in
the Superfamily Lebertiae.
Sperchonopsis verrucosa (Protz) (= Pseudosperchon verr .)
PL III, Fig. 34-36
Largest females may reach a length of 1.00 mm. ; males are
smaller. The body is elliptical, yellow brown. The large wart¬
like elevations of the dorsal side are found also on the posterior
ventral margin. The rostrum is long and slim. The medial an¬
terior ends of epimera I project and bear each a tuft of hairs.
The middle palpal segments are of about the same length, the
peg on the 2nd and 4th conspicuous. The genital organ lies close
to epimera IV ; the two anterior acetabula are elongated, the last
Marshall — Preliminary List of the Hydracarina 363
rounded. A small plate of chitin lying above the orifice distin¬
guishes the female.
This species is a bottom form and is cosmopolitan. It has
been found in Wyoming and California; in Wisconsin only in
Green Lake.
Literature Cited
Daday, E.
1905. Untersuch. fiber die Susswasser Mikrofauna Paraguays. Zoo-
logica, 18:272-326.
Koknike, F.
1912. A Revision of my “Nordamerikanische Hydrachniden”. Trans.
Canadian Inst: 281-298. Univ. Press, Toronto.
Lavers, C. H.
1941. A New Species of Limnochares from North America. Univ.
Washington Pub. in Biology, 12,No.l:l-6.
Lunrblad, O.
1934. Die Nordamerikanische n Arten der Gattung Hydrachna. Arkiv
f. Zoologi, 28 A, 3: 1-44.
1938. Neue Wassermilben aus Paraguay.
Zool. Anz., 122:7-19.
1941. Die Hydracarinenfauna Siidbraziliens und Paraguays. Kungl.
Sv. Vet. Akad. Handlingar, 19,7:1-183.
1941. Eine Uebersicht des Hydrachnellensystems etc. Zool. Bidrag.
Uppsala, 20:359-379.
1941. Neue Wassermilben aus Amerika, etc.
Zool. Anz., 133:155-160.
Marshall, R.
1926. Water Mites of the Okoboji Region.
Univ. Iowa Studies in Nat. His., 11,9:28-35.
1927. Hydracarina of the Douglas Lake Region.
Trans. Am. Micros. Soc., 46,4:268-285.
1929. Canadian Hydracarina.
Univ. Toronto Studies, Biol. Ser. Pub. OP.Res.Lab.39: 57-93.
1930. The Water Mites of the Jordan Lake Region.
Trans. Wis. Acad. Sci., 25:245-253.
1931. Preliminary List of the Hydracarina of Wisconsin. Part I.
Trans. Wis. Acad. Sci., 26:311-319.
1943. Hydracarina from California. Part I.
Trans. Am. Micros. Soc., 62,3:306-324.
1943. Hydracarina from California. Part II.
Trans. Am. Micros. Soc., 62,4:404-415.
Viets, K.
1933. Neue Hydrachna- und Eylais-Arten, etc., aus Porto Alegre,
Brasilien. Zool. Anz., 103: 161-171.
1936. Die Tierwelt Deutschlands.
Teil VII, 31,32 Teil, 574 pp. Jena.
1939. Wassermilben aus den Bayrischen Alpen, etc.
Arch. Hydrobiol., 36:72-93.
1940. Neue Hydrachnellae (Acari) aus Sudamerica.
Zool. Anz., 131:90-101.
364
Wisconsin Academy of Sciences, Arts and Letters
Plate I
1. Hydrachna canadensis , anterior dorsal structures
2. Hydrachna canadensis, left genital plate and epimera III, IV, nymph
3. Hydrachna canadensis , genital organ and right epimera III, IV, female
4. Hydrachna canadensis, right palpus, female
5. Hydrachna miliaria, anterior dorsal region, male
6. Hydrachna. miliaria, genital organ and right epimera III, IV, male
7. Hydrachna miliaria, right genital plate and epimera III, IV, nymph
8. Hydrachna miliaria, right palpus, female
9. Hydrachna magniscutata, right palpus, female
10. Hydrachna magniscutata, genital organ and right epimera III, IV, female
11. Hydrachna magniscutata, anterior dorsal region, nymph
12. Hydrachna magniscutata, dorsal plate
j
Marshall — Preliminary List of the Hydracarina
365
366
Wisconsin Academy of Sciences , Arts and Letters
Plate II
13. Hydrachna cruenta , dorsal plate
14. Hydrachna cruenta , genital organ and left epimera ID, IV, female
15. Hydrachna cruenta , dorsal plates, nymph
16. Hydrachna cruenta, right palpus, female
17. Hydrachna cruenta, genital plates and epimera in, IV, nymph
18. Hydrachna cruenta diminuata, dorsal plate
19. Hydrachna cruenta diminuata, genital organ and right epimera III, IV,
female
20. Hydrachna crenulata, left palpus
21. Hydrachna rotunda, lateral view
22. Hydrachna rotunda, genital organ and left epimera, female
23. Hydrachna rotunda, genital organ and left epimera III, IV, male
Marshall— Preliminary List of the Hydracarina 367
368
Wisconsin Academy of Sciences , Arts and Letters
Plate III
24. Hydrachna crenulata, genital organ and left epimera, male
25. Hydrachna crenulata, dorsal view
26. Hydrachna rotunda, left palpus, male
27. Limnochares aquatica, maxillary organ and palpus, lateral view
28. Limnochares aquatica, ocular plate
29. Limnochares aquatica, epimera III, IV and leg IV, left
30. Limnochare americana, ventral structures
31. Limnochares americana, ocular plate
32. Limnochares americana, leg IV, left
33. Limnochares americana, dorsal view
34. SperchoTiopsis verrucosa, ventral view, male
j5. Sperchonopsis verrucosa, right palpus
36. Sperchonopsis verrucosa, dorsal view
Marshall — Preliminary List of the Hydracarina 369
370
Wisconsin Academy of Sciences , Arts and Letters
Plate IV
37. Eylais infundibulifera bakeri, ocular plate
38. Eylais infundibulifera bakeri , left palpus
39. Eylais desecta, ocular plate, above
40. Eylais desecta , ocular plate, below
41. Eylais desecta, dorsal view
42. Eylais gibberipons hirsutipalpis, ocular plate
43. Eylais gibberipons hirutipalpis , palpus
44. Eylais robustus , ocular plate
45. Eylais robustus, ocular plate, irregular form
46. Eylais robustus, left palpus
47. Eylais falcata, ocular plate
48. Eylais rimosa, ocular plate
Marshall — Preliminary List of the Hydracarina 371
48
372 Wisconsin Academy of Sciences , Arts and Letters
Plate V
49. Hydryphantes tenuabilis , dorsal plate
50. Hydryphantes tenuabilis , palpus
51. Hydryphantes tenuabilis , rostrum, lateral view
52. Hydryphantes ruber, ventral view
53. Hydryphantes ruber, dorsal plate
54. Hydryphantes multiporus, genital organ
55. Hydryphantes multiporus, dorsal plate
56. Diplodontus despiciens, ventral plates
57. Diplodontus despiciens, dorsal view
58. Diplodontus despiciens, left palpus
59. Calonyx ovalis , leg IV, 6
60. Calonyx ovalis, ventral view, male
61. Calonyx ovalis, maxillary organ and palpus
62. Calonyx ovalis, genital organ, female
Marshall — Preliminary List of the Hydracarina
THE PHYSALOPTERA (NEMATODA) OF CARNIVORES
Banner Bill Morgan
Department of Veterinary Science , University of Wisconsin
The writer, in an attempt to identify some specimens of
physalopterid nematodes collected from various carnivores, was
unable to obtain complete descriptions of some forms because
several species were inadequately described. With this situation
a confusion exists in the literature as to which species are valid
and which are synonyms. There appear to be nine valid species
of Physaloptera recorded from carnivores. The purpose of this
paper is to present briefly what is known of the various species,
redescription of one species, a key to the species of Physaloptera
found in carnivores, and a world host list.
While making this study, material was loaned by Dr. A. B.
Erickson, University of Minnesota, Dr. E. A. Benbrook, Iowa
State College, and Dr. H. W. Brown, University of North Caro¬
lina. Specimens collected by the writer were examined as well
as supplementary material at the United States National Mu¬
seum Helminthological Collection, Washington, D. C.
In previous publications, Morgan (1941, 1942), in a sum¬
mary of North American Physalopterinae, reported that only
five species of Physaloptera had been shown to occur in North
American carnivores ; namely, P . felidis , P. maxillaris , P. prepn-
tialis , P. torquata, and P. rara. Five additional species have been
reported from carnivores from other parts of the world; P.
canis, P. anomala , P. terdentata, P. brevispiculum, and P. masoo-
di. The most common habitat of Physaloptera is the stomach
although they are occasionaly found in the small intestine. The
Physaloptera have a wide range in the Order Carnivora, having
been recorded from six Families ; Felidae, Canidae, Procyonidae,
Mustelidae, Hyaenidae, and Viverridae.
Physaloptera maxillaris Molin, 1860. Syn. P. semilanceo-
lata Molin, 1860; P. mephites Solanet, 1909; P. mydai
Baylis, 1926.
875
376 Wisconsin Academy of Sciences , Arts and Letters
Molin (1860) based his original description on specimens
taken from the stomach of a skunk ( Mephitis chinche) from
Brazil. Drasche (1883) substantiated P. maxillaris as a valid
species. Linstow (1889) reported P. maxillaris from Procyon
cancrivora (crab-eating raccoon) in Europe. Parona reported
this parasite from Mephitis suffocans (bare-nosed skunk) from
Argentina. Cameron (1936) identified P. maxillaris from the
intestine of Procyon cancrivora (crab-eating raccoon) captured
in Trinidad, British West Indies, on the basis of one female
specimen.
Physaloptera maxillaris was probably recorded for the first
time from North America by Ortlepp (1922) from Mephitis
mephitis (Canadian skunk) shipped from Canada to England.
Ortlepp (1922) also reexamined Molin’s type material and gave
a redescription of the parasite. Later, McClure (1930) reported
P. maxillaris from a Canadian skunk which had died in the New
York Zoological Gardens. In Mexico, Caballero and Peregrina
(1938) reported this parasite from the stomach of a hooded
skunk ( Mephitis m. macrura). Stegeman (1939) recorded P.
maxillaris from New York, in the stomach of Mephitis m. nigra
(Eastern skunk). Stiles and Baker (1935) did not list P. maxil¬
laris from North American hosts. The writer examined 147
skunks from Iowa, Illinois, and Wisconsin and found P. maxil¬
laris in 64 per cent of them. This parasite is one of the most
common in North America.
Physaloptera praeputialis Linstow, 1889. Syn. Chlamy-
donema felineum Hegt, 1910; C . praeputialis Travassos,
1917 ; C. praeputiale Yorke and Maplestone, 1926.
Linstow (1889) described P. praeputialis from a wildcat
( Felis catus) from Brazil. His description was based on several
females and one male specimen. Walton (1927) mentioned in
his revision of the Leidy collections the finding of a single female
specimen which was identified as P. praeputialis , from a non-
recorded host. In the host list Walton (1927) assigned this
specimen to the group “Mammal.” This is probably the first
record of P. praeputialis in North America. Later, Chitwood
(1931) reported the occurrence of this parasite for the first time
in the United States from Urocyon sp. (gray fox) from Virginia
and Lynx ruf us (lynx) Nevada. Caballero and Peregrina (1938)
Morgan — The Physaloptera (Nematoda) of Carnivores 377
reported this parasite from Mexico in the stomach of a lynx
( Lynx rufus texensis) and an ocelot ( Felis p. pardalis).
Physaloptera praeputialis was found by the writer eleven
times in 147 cats examined from Madison, Wisconsin and vi¬
cinity for an occurrence of 7.4 per cent. This parasite occurred
only in mild infections with one exception. One cat harbored
59 mature worms. From nineteen cats examined from Ames,
Iowa, seven were found infected. Two dogs examined from
Madison, Wisconsin and a silver fox from Wisconsin were found
infected with P. praeputialis .
Physaloptera torquata Leidy, 1886. Syn. P. papillotruncata
of Canavan, 1931.
Leidy (1886) described this species from Meles labridora
— Taxidea taxus (common badger) . Walton (1927) redescribed
the type material on the finding of male specimens. As the males
of the type specimens were immature with poorly developed
spicules, a further description was deemed necessary. Examina¬
tion of some of Leidy’s original material, dissection of the fe¬
males revealed two uteri without a common trunk. The re¬
description of P. torquata in this paper (Table I) is based on
material in the United States National Museum Helminthologi¬
cal Collection and specimens collected by the writer. Some of
this material was collected by Ehlers (1931) from Montana
badgers. Ehlers (1931) reported a complete history of the
pathology and symptoms of heavy infections of this parasite in
badgers.
Physaloptera rara Hall and Wigdor, 1918. Syn. P. cer -
docyona Sprehn, 1932; P. felidis Ackert, 1936; P. clausa
of Caballero and Peregrina, 1938; P. turgida of Leigh,
1940.
This parasite was described by Hall and Wigdor (1918) from
a single immature specimen removed from the duodenum of a
dog from Detroit, Michigan. The short esophagus described by
Hall and Wigdor has not been found in any other species of the
genus. To make the position more difficult, the type specimen of
P. rara cannot be located.
The writer has examined over 200 specimens of Physalop¬
tera from dogs, silver foxes, red foxes, gray foxes, wolves, and
cats. Several specimens were taken from dogs from the type
378
Wisconsin Academy of Sciences , Arts and Letters
Explanation op Plate
All figures except 10, 11, 12, 13, and 14; ventral view, male bursa of the
various species of Physaloptera found in carnivores. Scale not uniform.
Where scale appears, equals 1 mm.
Fig. 1. P. rara (Original) •
Fig. 2. P. maxillaris (Original).
Fig. 3. P. praeputialis (Original) .
Fig. 4. P. torquata (Original).
Fig. 5. P. anomala (After Ortlepp).
Fig. 6. P. brevispiculum (After Ortlepp, outer cuticle removed) .
Fig. 7. P. canis (After Monnig, outer cuticle removed) .
Fig. 8. P. masoodi (After Mirza, outer cuticle removed).
Fig. 9. P. terdentata (After Ortlepp).
Fig. 10. 2-A type uteri (Diagrammatic) .
Fig. 11. 2-B type uteri (Diagrammatic) .
Fig. 12. 2-C type uteri (Diagrammatic).
Fig. 13. Anterior end, lateral view of Physaloptera (Diagrammatic) .
Fig. 14. Anterior end, en face view of Physaloptera (Diagrammatic).
380 Wisconsin Academy of Sciences , Arts and Letters
locality. All appeared to agree with the description of Ackert
(1936) for P. felidis. However, the pair of small papillae de¬
scribed by Ackert (1936) appear to be phasmids. There is a
great variation in the diameter of the phasmids when observed
from a ventral view, which under certain conditions (over clear¬
ing) may be interpreted as small papillae.
Although P. rara was described from a single immature fe¬
male and is possibly an abnormal specimen, examination of many
specimens from the type host (dog) from the type locality (De¬
troit, Michigan) has convinced the writer that the parasite under
consideration is the same species. Thus, P. felidis has been
placed as a synonym of P. rara. In previous publications the
writer attempted to separate P. felidis and P. rara but all identi¬
fications should now be regarded as P. rara.
Ackert (1936) described P. felidis = P. rara from local Kan¬
sas cats. Whitlock (1937) reported this parasite quite common
in Kansas. Ackert (1941) examined 193 adult cats from the
vicinity of Manhattan, Kansas, and 88 or 45.6 per cent were
infected with this parasite. Olson et al (1937) reported P. felidis
— P. rara from a coyote killed near Hubbard County, Minnesota.
Immature specimens of Physaloptera from dogs have been re¬
corded by Secord (1933) and Baker (1941).
Physaloptera pacitae Tubangui, 1925, from the domestic cat
{Felis domestica) Philippine Islands; P. papilloradiata Linstow,
1889, from Canis lupus (wolf) Persia; P. cesticillata Sonsino,
1889; from Canis cerdo (Fennec fox) Egypt; and P. elegantis-
sima Stossich, 1902, female specimens from Ratelus capensis
(honey badger) Eritrea; have all been inadequately described.
Physaloptera gemina Linstow, 1899, from the domestic cat and
P. vandenbrandeni Gedoelst, 1924, from a wildcat ( Felis sp.)
from Belgian Congo; have been allocated to the genus Abbrevi-
ata.
Parasite Host List of Physaloptera Found in Carnivores
1. Physaloptera rara — Canidae. Canis familaris (domestic
dog) Hall and Wigdor, 1918; Michigan. Morgan, 1941, 1942,
Wisconsin, Michigan, Tennessee. C. latrans (coyote) Olson,
Fenstermacher, and Pomeroy, 1937, Minnesota; Erickson, 1941,
Minnesota; Morgan, 1941, 1942, Iowa, Mississippi. C. nubilus
(timber wolf) Erickson, 1941, Minnesota; Morgan, 1941, 1942,
Morgan~The Physaloptera ( Nematoda ) of Carnivores 381
Nebraska, Kansas, North Dakota, South Dakota. C. n. nebracen-
sis (prairie wolf) Morgan, 1941, 1942, Nebraska. C. ochropus
(valley coyote) Ibid , California. Urocyon c. cinereoargenteus
(Eastern gray fox) Ibid , Virginia, Eastern United States. U. c.
calif ornicus (California gray fox) Ibid , California. £7. c . ftori-
danus (Florida gray fox) Ibid , Arizona; Caballero and Pere-
grina, 1938, Mexico. U. c. ocythaus (Wisconsin gray fox) Erick¬
son, 1941, Minnesota; Morgan, 1941, 1942, Wisconsin. VuLpes
fulva (silver and eastern red fox) Morgan, 1941, 1942, Wiscon¬
sin, Minnesota. V . regalis (Northern plains red fox) Ibid , Iowa.
Cerdocyon azeaus (wolf -like fox) Sprehn, 1932, Germany. Pro-
CYONIDAE. Procyon l. lotor (Eastern raccoon) Morgan, 1941,
1942, Wisconsin, Iowa; Leigh, 1940, Illinois. Felidae. Felis
domestica (domestic cat) Ackert, 1938, 1941, Kansas; Whit¬
lock, 1937 ; Kansas ; Morgan, this paper, Wisconsin. Lynx rufus
(bobcat) Erickson, 1941, Minnesota.
2. P. maxiliaris — Mustelidae, Procyonidae. A complete
host list of this parasite has been recorded in a previous publi¬
cation, (Morgan, 1943).
3. P. praeputialis — Felidae. Felis catus (wildcat) Linstow,
1889, Brazil. P. domestica (domestic cat) Hegt, 1910, Batavia;
Gedoelst, 1911, Belgium; Bodkins and Cleare, 1916, British
Guiana; Travassos, 1917, Brazil; Ortlepp, 1922, Federated
Malay States, China, Ceylon, Dutch Guiana, British Guiana;
Chandler, 1925, India ; Faust, 1929, Chen, 1934, Tang, 1936, An¬
drews, 1937, all from China; Pinto, 1936, Brazil. Landa, 1934,
Eastern Russia; Neuland, 1934, Southwest Russia; Volkenberg,
1939, Puerto Rico; Foster, 1939, Panama; Morgan, 1941, 1942,
Wisconsin, Iowa; Benbrook, 1940, Iowa; Sandground, 1940, In¬
diana. F. tigra (Malay tiger) Harrison and Hall, 1909, London
Zoo. F.nebulosa (clouded leopard) Ortlepp, 1922, India; Chand¬
ler, 1925, India. F. pardus (leopard) Ortlepp, 1922, Nigeria;
Monnig, 1923, South Africa; Sandground, 1928, Tanganyika.
F. tigrinum (tiger) Thwaite, 1927, Ceylon; Boulenger, 1923,
Zanzibar. F. caff r a (eaffra cat) Monnig, 1923, South Africa.
F. p. pardalis (ocelot) Caballero and Peregrina, 1938, Mexico;
F. bengalensis (leopard cat), F. viverina (fisher cat) Travassos,
1917, Brazil; F. cougar (mountain lion) Morgan, 1941, 1942,
West Virginia. Lynx rufus texensis (lynx or bobcat) Caballero
and Peregrina, 1938, Mexico; Lynx rufus (bobcat) Chitwood,
382 Wisconsin Academy of Sciences, Arts and Letters
1931, Nevada; Spurlock, 1940, California. L. uninta (mountain
bobcat) Morgan, 1941, 1942, Oregon. Lynx rufus baileyi (Bailey
bobcat), Crater, 1936, Arizona. Lynx canadensis (bobcat) Mor¬
gan, 194l!, 1942, Canada. Canidae. Canis familiaris (domestic
dog) Morgan, 1941, 1942, Wisconsin ; Pinto and Almeida, 1935,
Brazil ; Stiles and Baker, 1935, location not given ; Andrews,
1937, China. C. mesomelas (black-backed jackal) Monnig, 1923,
South Africa. Urocyon sp. (gray fox) Chitwood, 1931, Virginia.
U. c. cinereoargentaus (Eastern gray fox) Morgan, 1941, 1942,
Iowa. U. c. borealis (Northern gray fox) New Hampshire, Ibid.
Vulpes fulva (silver fox) Morgan, 1941, 1942, Wisconsin. Vi-
VERRIDAE. Genetta ludia (genetta cat) Monnig, 1923, South
Africa.
Table I. Comparative measurements of P. torquata
4. P. torquata — Mustelidae. Taxidea t. taxus (common
badger) Leidy, 1886, Pennsylvania ; Walton, 1927, Pennsyl¬
vania ; Morgan, 1941, 1942, Wisconsin, Illinois ; Canavan, 1931,
Philadelphia Zoological Gardens. T . t. neglecta (Western bad¬
ger) Ehlers, 1931, Montana ; Hannum, 1939, Arizona ; Morgan,
1942, California. Procyonidae. Procyon l. lotor (Eastern rac¬
coon) Morgan, 1942, Wisconsin, Iowa.
5. P. anomala Molin, 1860. Felidae. Fells onca (jaguar)
Molin, 1860, Brazil. Ortlepp, 1924, Dutch Guiana.
6. P. brevispiculum Linstow, 1906. Syn. P. malayensis Ort¬
lepp, 1922. Chlamydonema fuelleborni Mirza and Narain, 1934.
Felidae. Fells rubiginosa (rusty-spotted cat) Linstow, 1906,
Morgan — The Physaloptera ( Nematoda ) of Carnivores 383
Table II. Comparative measurements of P. maxillaris
Comparative measurement of P. rara
Comparative measurement of P. praeputialis
384 Wisconsin Academy of Sciences , Arts and Letters
Ceylon. F. chaus (jungle cat), F. tigris (tiger), “Tiger Cat/’
Ortlepp, 1922, Federated Malay States, “Bush Cat” Nigera. F.
domestica (domestic cat) Mirza and Narain, 1934, India. Hy-
aendae. Hyaena striata (hyaena) Ortlepp, 1922, Nigeria.
7. P. canis Monnig, 1929. Canid ae. Canis familiaris (do¬
mestic dog) Monnig, 1929, South Africa. Felidae. Felis domes¬
tica (domestic cat) Monnig, 1938, South Africa.
8. P. masoodi (Mirza, 1934). Syn. Chlamydonema masoodi
Mirza, 1934. Felidae. Felis chaus (jungle cat) Mirza, 1934,
India.
9. P. terdentata Molin, 1860. Syn. P. digitata Schneider,
1866. Felidae. Felis concolor (puma) Molin, 1860, Brazil.
Schneider, 1866, Brazil. F. tigrina (tiger) Molin, 1860, Brazil.
F. pardus (leopard) Shipley, 1905, Sudan.
Key to Species of Physaloptera Found in Carnivores
1. Female with 2- A uteri . 2
Female with 2-B uteri . 3
Female with 2-C uteri . 5
2. Male with 5 pairs of post anal papillae; 2 pair surrounding cloaca; 1 pair
directly behind center pair of cloacal papillae; 2 pairs equidistant on tail;
3 pre-anal papillae . P. anomala Molin, 1860
Male with 5 pairs post anal papillae; 2 pairs surrounding cloaca; 3 pairs
equidistant on tail; 3 pre-anal papillae . P. maxillaris Molin, 1860
3. Male with 5 pairs post anal papillae; 2 pairs surrounding cloaca; 3 pairs
equidistant on tail; 3 pre-anal papillae . 4
4. Spicules slightly unequal; left spicule 604 to 931^; right spicule 532 to
791^; right spicule with definite twist . P. torquata Leidy, 1886
Spicules slightly unequal; slightly curved, slender; left spicule 740 to 924^;
right spicule 477 to 700^ . P. rara Hall and Wigdor, 1918
5. Vulva in middle of body . 6
6. Male with 5 pairs post anal papillae; 2 pairs surrounding cloaca; 3 pairs
further down on tail; 3 pre-anal papillae . P. canis Monnig, 1929
7. Vulva in anterior third of body . 8
8. Male with 3 pairs post anal papillae; 1 unpaired papillae; 2 pairs sur¬
rounding cloaca; 3 papillae in transverse row near tip of tail; 3 pre-anal
papillae . P. masoodi (Mirza, 1934)
Male with 5 pairs post anal papillae; 2 pairs surrounding cloaca; 1 pair
directly behind center pair of cloacal papillae, 2 pairs equidistant on tail;
3 pre-anal papillae . P. praeputialis Linstow, 1889
9. Male with 5 pairs post anal papillae; 2 pairs surrounding cloaca; 3 pairs
further down on tail; 3 pre-anal papillae . 10
10. Spicules long, unequal, slightly curved; left spicule 1.4-2.5 mm., right
spicule 580-597 ^ . P. brevispiculum Linstow, 1906
Spicules short, equal, or subequal; left spicule 320^ right spicule 305^ ....
. P. terdentata Molin, 1860
Morgan — The Physaloptera ( Nematoda ) of Carnivores 385
Literature Cited
Ackert, J.
1936. Physaloptera felidis n. sp. A nematode of the cat. Trans. Amer.
Micro. Soc. 65: 250-254.
Ackert, J.
1941. The cat as a host of the nematode Physaloptera felidis Ackert.
1941. Rev. Med. Trop. y Parasitol. Bact. Clin, y Lab. 7: 7-8.
Andrews, N.
1937. Helminth parasites of dogs and cats in Shanghai, China. Jour.
Helminth. 15: 145-152.
Baker, D.
1941. Physaloptera in New York state dogs. Cornell Vet. 31: 80-82.
Baylis, H.
1926. Some parasitic worms from Sarawak. Sarawak Mus. Jour. 3:
303-322.
Bodkins, G. and Cleare, L.
1916. Notes on some animal parasites in British Guiana. Bull. Ent.
Res. 7: 179-190.
Boulenger, C.
1923. A collection of nematode parasites from Zanzibar. Parasitology.
15: 113-121.
Caballero, E. and Peregrina, D.
1938. Nematodos de los mamiferos de Mexico. Anales Inst. Biol. 9:
289-306.
Cameron, T.
1936. Studies on the endoparasitic fauna of Trinidad. III. Some para¬
sites of Trinidad Carnivores. Can. Jour. Res. 14: 25-38.
Canavan, W.
1931. Nematode parasites of vertebrates in the Philadelphia Zoologi¬
cal gardens and vicinity. Parasitology. 23: 196-229.
Chandler, A.
1925. The helminths of cats in Calcutta, and the relation of cats to
human helminthic infection. Indian Jour. Med. Res. 13: 213-228.
Chen, H.
1937. Some parasitic nematodes from mammals of South China. Para¬
sitology. 29: 419-434.
Chitwood, B.
1931. Jour. Parasitol. 18: 53.
Crater, R.
1936. Jour. Mammal. 17: 170-171.
Drasche, R.
1883. Revision der in der nematoden. Verhandl. Zool. Bot. Gesell.
Wien. 32: 117-218.
Ehlers, G.
1931. The anthelmintic treatment of infestations of the badger with
Spirurids ( Physaloptera sp.). Jour. Amer. Vet. Assoc. 31: 79-87.
Faust, E.
1929. The animal parasites of the dog and cat in China. Lingnan
Sci. Jour. 8: 27-44.
886 Wisconsin Academy of Sciences , Arts and Letters
Foster, A.
1939. Some helminthic parasites recovered from domesticated ani¬
mals (excluding equines) in Panama. Proc. Helm. Soc. Wash. 6:
101-102.
Gedoelst, L.
1924. Notes on parasitologie Congolaise. Ann. Soc. Belg. Med. Trop.
4: 1-7.
Hall, M. Wigdor, M.
Physaloptera from the dog, with a note on the nematode parasites of
the dog in North America. Jour. Amer. Vet. Med. Assoc. 6: 733-744.
Harrison, M. and Hall, I.
1909. Fatal enteritis in a tiger caused by Physaloptera praeputialis .
Parasitology 2: 29-31.
Hegt, J.
1910. Chlamydonema felineum, Nov. Gen. Nov. Sp., eine neue para-
sitch lebende Nematode. Tijdsch. der Nederl. Dierk. Vereen. 12:
5-59.
Korke, V.
1928. Revision of type species of Linstow in India. Indian Jour.
Med. Res. 16: 199-202.
Landa, D.
1934. Biological Abstracts. 8: 679.
Leidy, J.
1886. Notices of nematoid worms. Proc. Acad. Nat. Sci. Philadelphia.
38: 308-313.
Leigh, W.
1940. Preliminary studies on parasites of upland game birds and fur¬
bearing mammals in Illinois. Ill. Nat. Hist. Survey Bull. 21: 185-194.
Linstow, O.
1889. Helminthologisches. Arch. fur. Nat. 54: 235-246.
1899. Nematoden Aus der Berliner Zoologischen Sammlung. Mitt.
Zool. Mus. 1: 5-28.
McClure, G.
1930. Nematode parasites of mammals. Zoologica. 15: 1-28.
Monnig, H.
1923. South African parasitic nematodes. Rept. Direct. Vet. Ed. Res.
9/10: 435-478.
Monnig, H.
1929. Physaloptera canis, n. sp., A new nematode parasite of the dog.
Rept. Direct. Vet. Ser. Union. South Africa 15: 329-333.
Molin, R.
1860. Una monografia del genere Physaloptera. Sitzungsb Akd. d.
Wissemsch. 39: 637-672.
Morgan, B. B.
1941. A summary of the Physalopterinae (Nematoda) of North Amer¬
ica. Proc. Helm. Soc. Wash. 8: 28-30.
1941. Additional notes on North American Physalopterinae (Nema¬
toda). Ibid., 8: 63-64.
Morgan — The Physaloptera ( Nematoda ) of Carnivores 387
1942. The Physalopterinae (Nematoda) of North American verte¬
brates. Sum. Doctoral Diss. Univ. Wis. 6: 88-91.
1943. The Physalopterinae (Nematoda) of Aves. Trans. Amer. Micro.
Soc. 62: 72-80.
1943. The Physaloptera (Nematoda) of Rodents. Wassmann Collector.
5: 99-107.
1943. The Physaloptera (Nematoda) of Reptiles. Le Nat. Can. 70: 179-
185.
Mirza, M.
1934. Chlamydonema masoodi n. sp. Ann. Parasitol. 12: 367-370.
Mirza, M. and Narain, S.
1934. Chlamydonema fuellebomi n. sp. Current Sci. Bangalor. 2: 288.
Neuland, D.
1934. Biological Abstracts. 8: 971.
Olson, O., Fenstermacher, R., and Pomeroy, B.
1937. The coyote as a host to Physaloptera felidis. Cornell Vet. 27:
327.
Ortlepp, R.
1922. The nematode genus Physaloptera Rud. Proc. Zool. Soc. London.
999-1107.
Ortlepp, R.
1924. On a collection of helminths from Dutch Guiana. Jour. Hel-
minthol. 2: 15-40.
Pinto, C.
1936. Physaloptera dos catos do Brasil. O. Campo. 7: 45.
Pinto, C. and Almeida, J.
1935. Sinopse dos helmintos dos animois domesticos do Brasil. O.
Campo. 6: 60.
Sandground, J.
1928. Some new cestode and nematode parasites from Tanganyika
territory. Proc. Boston Soc. Nat. Hist. 39: 131-150.
Schneider, A.
1866. Monographic der Nematoden. 1-357.
Secord, A.
1933. A study of nematodes found in dogs from Franklin County,
Ohio. Ohio State Univ. Vet. Alum. Quart. 21: 9-19.
Shipley, A.
1905. Notes on a collection of parasites belonging to the Museum of
University College, Dundee. Proc. Cambridge, Phil. Soc. 13: 95-102.
Solanet, E.
1909. Sobre una Physaloptera del Mephites sutfocans. Rev. centro.
Est. Agron. y. Vet. 90-92.
Sprehn, C.
1932. Uber einige von Dr. Eisentraut in Bolivien gesammelte Nema¬
toden. Zool. Anz. 100: 273-294.
Stegeman, L.
1939. Some parasites and pathological conditions of the skunk ( Me¬
phitis mephitis nigra ) in Central New York. Jour. Mammal. 20: 493-
388 Wisconsin Academy of Sciences , Arts and Letters
Stiles, C. and Baker, C.
1935. Key catologue of parasites reported for Carnivora, with their
possible public health importance. Nat. Inst. Health Bull. No. 163.
Stossich, M.
1889. II Genere Physaloptera Hud. Bull. Soc. Adriat. Sci. Nat. Trieste.
2: 1-24.
Tang, C.
1936. A survey of helminth fauna of cats in Foochow. Peking Nat.
Hist. Bull. 10: 223-231.
Thwaite, J.
1927. On a collection of nematodes from Ceylon. Ann. Trop. Med.
Parasitol. 21: 225-244.
Travassos, L.
1917. Infermacoes sobre um interessante parasito dos gatos. Arch.
Eseola Sup. Agric. Med. Vet. 1: 101-103.
Tubangui, M.
1925. Metazoan parasites of Philippine domesticated animals. Philip¬
pine Jour. Sci. 28: 11-35.
Walton, A.
1927. A revision of the nematodes of the Leidy collection. Proc. Acad.
Nat. Sci. Philadelphia. 79: 49-163.
Whitlock, J.
1937. Endoparasitism of the cat. Vet. Med. 32: 514-520.
Yorke, W. and Maplestone, B.
1926. Nematode parasites of vertebrates. London.
WINTER OXYGEN CONTENT AND BIOCHEMICAL
OXYGEN DEMAND IN A WISCONSIN
ARTIFICIAL LAKE
Charles H. Lewis and Neil E. Stevens
University of Illinois
The oxygen content of lake and reservoir water under ice is
important in the culture of at least two Wisconsin food crops,
fish and cranberries. The direct relation between the oxygen
content of water under ice and the death of fish by smothering
has long been known. Recently it has become recognized that
certain important and widespread cranberry troubles known
as leafdrop, flower bud absorption, etc., may be caused or ag¬
gravated by a deficiency of oxygen in the water in which they
are submerged. In extreme cases the vines may be killed out¬
right.
In connection with a study of cranberry problems we have
gathered the information on the winter oxygen content of water
presented below. Much of the work here recorded was carried
out in the laboratory of Wisconsin Conservation Department at
Spooner, Wisconsin. For permission to use this laboratory, and
for helpful suggestions, we are indebted to D. J. O’Donnell, biol¬
ogist of the Wisconsin Conservation Department.
The reservoir studied is in Washburn County. It was made
in 1912 by damming up Beaver Brook at which time it covered
about forty acres. Because of reduced rainfall it was found
necessary from 1930 to conserve water by pumping it back into
the reservoir from the marsh, and in 1934 to supplement the
flow of the brook by pumping it from a deep well. The area of
the reservoir has been gradually increased by raising the dam,
and is now approximately one hundred acres. All of this, except
the bed of Beaver Brook itself, was originally covered with vege¬
tation. There are numerous tree stumps still in the reservoir.
The water in the reservoir is relatively hard, varying in pH
from 7.6 to 8.2.
The present paper is based on about 300 separate determina-
389
390 Wisconsin Academy of Sciences , Arts and Letters
tions and gives a practically continuous record of the oxygen
content and biochemical oxygen demand of the water from the
time the reservoir first froze over in the fall until the ice melted
in the spring. So far as we have been able to discover no similar
data have been published.
Oxygen Content
Determinations of the dissolved oxygen content were made
by the modified Winkler method, following exactly the directions
given by the Wisconsin Department of Health in the Wisconsin
Sewage Works Operators' Short Course. The standardized solu¬
tions and many of the chemicals used were furnished by Dr. W.
B. Griem, chemist of the Wisconsin Department of Agriculture.
In all, several hundred determinations were made at a series of
stations spaced at intervals over the reservoir. Although there
are naturally some slight variations from place to place they do
not appear to be constant or significant. Consequently the fig¬
ures from only one representative station are given in the
graphs.
Ice covered the reservoir November 26, 1942. Determina¬
tions were begun November 29 at which time the ice was five
12/1 1/1 2/1
DISOLVEO
OXYGEN
12
II
10
9
8
7
6
5
4
3
2
I
0
Lewis and Stevens — Winter Oxygen Content and Demand 391
inches thick and covered with less than an inch of snow. The
ice increased in thickness up to twenty inches on about March
26, and was covered with snow most of the winter. The depths
from which the samples were taken are measured in feet from
the top of the ice. As is evident from the graph, throughout the
month of December the oxygen content of the water declined
fairly steadily from 10.5 to 7 parts per million at a depth of two
feet and from 10 to 2.2 parts per million at a depth of six feet.
A corresponding difference in the oxygen content at the different
depths was observed at all stations. During January, 1943,
there was a rapid decline in the oxygen at both levels and by
February 27 it had reached a point so near zero that our de¬
terminations can no longer be considered significant. These
conditions remained unchanged except for a slight but measur¬
able rise about February 26 to 27 caused by pumping back large
quantities of water used in flooding the marsh on February 24.
Between March 25 and 31 the reservoir was raised one foot by
melting ice and snow, and there was a marked rise in oxygen
content which was still further increased by pumping on April
5, 6 and 7. It should be added that by the first of February it
was evident that most of the fish were dead. The only fish to
VI
4/1
,\
/
I
BIOCHEMICAL
OXYGEN DEMAND
14
13
12
II
10
9
8
7
6
S
4
3
2
392 Wisconsin Academy of Sciences , Arts and Letters
survive the winter were the larger ones that were able to mi¬
grate to the springs.
Biochemical Oxygen Demand
The biochemical oxygen demand was determined by the
methods outlined in the directions mentioned above. This is a
somewhat simplified form of the directions given in “Standard
Methods of Water Analyses. 1936.,, The biochemical oxygen
demand of a water sample is expressed in terms of the difference
of the amount of dissolved oxygen in a sample of thoroughly aer¬
ated distilled water, and a similar sample of aerated distilled
water with which has been mixed a known quantity of the water
to be tested, after both samples have been incubated at the same
temperature for the same length of time. In the results here
reported 50 cc. of the reservoir water was mixed with 200 cc.
of aerated distilled water and incubated at 20° C. for five days.
It is thus a measure of the extent and to some degree of the rate
with which such reservoir water may be expected to exhaust the
oxygen present in any water with which it may become mixed.
In Wisconsin this measure is widely used in studies of sewage
and mill wastes which enter rivers.
As is evident from the graphs, the biochemical oxygen de¬
mand of the water of the reservoir at Beaver Brook rose slightly
during December when the oxygen content of the water was
above 3 parts per million and from this point rose more rapidly
until shortly after February 26 when a considerable supply of
freshly aerated water was pumped back from the marsh. The
effect of this added oxygen is clearly shown by the fact that the
biochemical oxygen demand of the reservoir water was materi¬
ally less on March 3 and March 16. By the end of the month the
biochemical oxygen demand was equal to or greater than before
the pumping. Between March 25 and 31, the reservoir rose a
foot from melting ice and snow. This raised the oxygen content
of the water at the two-foot level to 6.7. On April 2 the marsh
was flooded, removing at least two-thirds of the water from the
reservoir. Much of this water was pumped back and this, to¬
gether with the rapid accumulation of melting ice and snow,
filled the reservoir by April 7. At this time the oxygen content
of the water was approximately 8 parts per million at all levels.
It should be especially noted, however, that while the biochemi-
Lewis and Stevens — Winter Oxygen Content and Demand 393
cal oxygen demand was much lower on April 7 than on March
31, before the water was aerated, it was by no means reduced
to zero ; in fact it was still measurable nine days later.
Significance of these Observations
in Cranberry Culture
In a recent paper, Bergman has summarized the available
information regarding injury to cranberry vines due to de¬
ficient oxygen under the ice. His researches have established
the fact that injury may occur whenever the oxygen content of
the water drops below four parts per million for a sufficient
length of time.
The observations here recorded indicate that the cranberry
grower who has experienced trouble from smothering during the
winter, when flooding his marsh, must consider not only the
oxygen content of the water but its biochemical oxygen demand.
It is comparatively easy, as shown in Table I, to aerate water by
Table I. Increase in oxygen content of water following
splashing over gates.
Sowing through gates and over a series of splash boards. The
biochemical oxygen demand of this same water may, however,
be so high that the oxygen is quickly exhausted. This is strik¬
ingly illustrated by the observations made on a typical field at
Beaver Brook and recorded in Table II.
In spite of the fact that water was continuously flowing into
the marsh from the reservoir the oxygen content dropped in the
394 Wisconsin Academy of Sciences, Arts and Letters
Table n. Decrease in oxygen content of water on a cranberry field.
second day to 5.9. Within twenty-four hours after the flow from
the reservoir was stopped the oxygen content dropped to 2.8.
Under these conditions there appears to be no safe course but
continual sampling. As soon as the oxygen content nears the
danger point it must be raised by the addition of freshly aerated
water.
FURTHER OBSERVATIONS ON ALKALINE
FLOODING WATER IN CRANBERRY GROWING
Neil E. Stevens
University of Illinois
Additional evidence (1) of the apparently injurious effect of
alkaline flooding water in cranberry culture has been derived
recently from three distinct sources.
First, and in some respects most significant, is the fact that
two successive crops of cranberries have been produced on the
only marsh now cultivated in the Berlin area. These crops were
not large in comparison with the most productive Wisconsin
marshes. They were, however, commercial crops far larger than
any produced there for many years. The only changes in culture
methods relate to the handling of the water. The water in the
ditches was held at a lower level by pumping, when necessary,
into the canal leading to the Fox River. During both growing
seasons, river water was excluded from the marsh, also by pump¬
ing when necessary. Until September, 1943, the water used in
flooding the marsh came entirely from the reservoir the level
of which was raised nearly a foot in 1943. Under the conditions
of precipitation obtaining in 1942 and 1943, the water in the
reservoir came chiefly from rain and melted snow. The pH of
the reservoir water during these two years was about 6.8. This
figure is an average of the readings taken at five different sta¬
tions twice during 1942 and several times in 1943.
The second piece of evidence relating to this general subject
was the unexpected, and as yet unexplained, effect of adding
sodium bicarbonate to the flooding water. Some 160 pounds of
technical sodium bicarbonate were added to the reservoir water
(pH about 5.3) used in flooding about an acre of cranberries on
June 10, 1943. The cranberries were submerged for less than
sixteen hours. There followed an extremely heavy vegetative
growth whose abundance was lacking on adjacent sections flood¬
ed at the same time with untreated water. Whatever the ex-
395
396 Wisconsin Academy of Sciences , Arts and Letters
planation of this may be, the fact is significant in relation to the
history of marshes with alkaline flooding water.
Finally, further study* of the history of cranberry culture in
the Berlin area has brought out several very important points
not wholly clear hitherto and indicates an even closer relation
between the yield of cranberries in the Berlin area and the use
of alkaline water than was suggested in the earlier paper. The
famous crop of 1872 in this area was the high point in a series
of good crops. The canal from Willow Creek at Auroraville to
the Carey marsh was dug in 1878. This was the first use of
alkaline water in large amounts in this region. The other canals,
that connecting Willow Creek with the Walters’ and nearby
marshes and that connecting the Fox River with the Sacket
Marsh, were not dug until more than ten years later. Because
of the importance of these facts in relation to the general prob¬
lems of the history and geography of cranberry culture in Wis¬
consin, such figures relating to the actual crops as appear in the
Berlin Conrant are given in Table I.
Curiously enough there appears no estimate of the 1872 crop
for the Berlin area. There is, however, abundant collateral evi¬
dence that it was very large. The figures given for Carey (10,-
000) and Sacket** (8,000) are based on berries actually har¬
vested and in at least one case this was before picking was fin¬
ished, so they are too small rather than too large. Moreover, we
have some figures on the number of pickers. The following note
appeared in the Berlin Courantt September 26, 1872.
“We understand that on Carey’s marsh there have been
an average of 1,500 pickers and on Sackett’s 1,200. On
Sacket’s marsh there have been already 8,000 barrels
picked. . . . Somewhere in the vicinity of $50,000 are paid
for cranberry picking in this locality.”
The following week the Courant also reported that pickers on
Carey’s marsh held a straw vote in the presidential campaign in
which Greeley got 1,117, Grant 340. As a means of predicting
the outcome of the election this is about as good as the Literary
* This involved reading all items relating to cranberries in the Berlin Courant, a nearly corn-
complete file of which is available in the library of the Wisconsin State Historical Society. In this
work considerable assistance was given by various members of the staff of the State Entomologist,
particularly Mr. Noel F. Thompson. The Berlin Evening Journal, established in 1881, has also
been a useful source of information.
** In the earlier paper the name Sacket is incorrectly spelled, and H. S. Sacket, whose owa
work was important is given credit for the pioneer work of his father, Edward.
Stevens — Akaline Flooding Water in Cranberry Growing 397
Table I. Cranberry statistics from the Berlin, Wisconsin, area.
Reported Yield in Barrels
*A preliminary estimate with the comment “much larger than ever before”
A preliminary estimate as picking started
No estimates are available for the crops of the Carey Marsh 1873-1878, but
evidence that they were not too good is found in a report published in the
Berlin Evening Journal August 7, 1885,
“James Carey says prospects on the Carey Marsh are better this
year than at any time since 1872, the year of the big crop.”
Digest poll of 1936, but it does prove that the Careys had almost
1,500 pickers.
The regular price for picking cranberries in the Berlin area
in 1872 was 75 cents a bushel as indicated by the C our ant of
August 29. If the estimate that $50,000 was paid pickers that
year is approximately correct, that would equal an estimated
yield of 66,000 bushels or 22,000 barrels. Moreover, if Sacket
with 1,200 pickers had harvested 8,000 barrels by September 26,
then it is obvious that the Careys with a much larger crew may
well have had more than the 10,000 barrels with which they
have usually been credited.
The preliminary estimate of 30,000 for 1874 gains some sup¬
port from the statement, published September 12, 1874, of a re¬
porter who had recently visited the marshes, that Sacket's Marsh
had over 800 pickers and Carey's 1,600. No doubt labor condi¬
tions would affect the number wanting to pick cranberries, but
the large number of pickers would probably indicate a good crop
of cranberries.
398 Wisconsin Academy of Sciences , Arts and Letters
I do not wish to labor a point which may already be as fully
established as it can be by any evidence not experimental, but
it is apparent that the Carey Marsh became less productive fol¬
lowing the introduction of alkaline water from Willow Creek in
1873. On the evidence of Daniels (2), writing from Auroraville
in 1878, other marshes had been “more remunerative during the
last two years.” This and adjacent marshes became unprofitable
and have long since been abandoned. The Sacket Marsh also
seems to have been less productive following the use of alkaline
water from the Fox River after 1885.
In all fairness it should be added that in the conclusions here
drawn I find that I am putting in print a conviction long held by
a number of the older residents of Berlin and Aurora. They
firmly believe that the decline of cranberry growing in that area
dates from and was caused by the introduction of water from
Willow Creek and Fox River. Their courtesy and kindliness to
an inquisitive stranger surely deserves this brief acknowledge¬
ment.
Literature Cited
1. Stevens, N. E., Rogers, L. M., and Bain, H. F.
1940. Alkaline flooding water in cranberry growing. Trans. Wis.
Acad. Sci., 32: 351-360.
2. Daniels, E. W.
1878. Cranberries in Waushara County. Trans. Wis. State Hort. Soe.
8: 140-143.
A SURVEY OF THE WISCONSIN LIME INDUSTRY
Kenneth Bertrand
The burning of lime is one of the oldest manufacturing in¬
dustries in Wisconsin. As such, it spans the transition from a
pioneer to a highly integrated industrial economy. It therefore
provides an example of the effect on industry of technological
change, variation in market demands, and depletion of cheap
fuel supplies. Insofar as the Wisconsin lime industry has been
unable to adjust itself to these changes, it has suffered serious
decline. It is the purpose of this survey to explain the causes of
this decline, which is clearly shown in Figures 1 and 2.
From 1904 to 1940 the amount of lime sold by producers in
the nation as a whole increased 80 per cent, from 2,707,809 tons
to 4,886,929 tons. In the same period Wisconsin producers suf¬
fered a decline of 65 per cent.1 In 1940 the eleven producers in
Wisconsin sold 65,632 tons of lime, in contrast to 244,903 tons
sold by 25 operators in 1925. In this year the latest peak of
production was reached, followed by the decline from which the
industry has not been able to extricate itself. As shown in Fig¬
ure 1, production was fairly uniform from 1904 until 1925
except for the temporary decline during and following the first
World War. From 1907 to 1914 Wisconsin ranked third in the
nation, following the major producers, Pennsylvania and Ohio,
and until 1925 was rarely lower than fifth. By 1940 Wisconsin
ranked thirteenth. In 1908 Wisconsin producers sold 8.5 per
cent of all the lime sold in the nation ; in 1940 they contributed
only 1.3 per cent.
Historical Development
The date of the construction of the first lime kiln in Wiscon¬
sin is not certain, but lime is known to have been burned in crude
1 Unless otherwise indicated all statistics used in this paper are taken from the section on lime
appearing annually from 1904 to 1923 in the Mineral Resources of the United States, U. S. Geol.
Surv., Dept, of Interior. From 1924 to 1931 the figures are from Mineral Resources of the United
States, Bur. of Mines, U. S. Dept, of Commerce. From 1932-33 to 1940 figures are from Minerals
Year Book, Bur. of Mines, U. S. Dept, of Int. These figures show lime sold by producers and
consumed by producers in the various states and are equivalnet to lime produced.
399
400 Wisconsin Academy of Sciences , Arts and Letters
kilns constructed in the fields by the first settlers to obtain lime
for mortar and whitewash.2 In places where the soil was stony
the rock to be burned was collected from the newly cleared fields.
The number of commercial kilns increased to meet the growing
demand for lime created by rapid development of the state from
1850 to 1880. Great quantities of otherwise unmarketable local
cordwood provided an abundant supply of cheap fuel. Those
kilns which were near enough to Lake Michigan to be able to
ship by water were the first to expand beyond the local market.3
Others began production for distant consumers as railroads ex¬
tended their lines through southern and eastern Wisconsin. The
industry developed rapidly on the stimulus provided by such
rapidly growing cities as Milwaukee and Chicago, far removed
from competition of eastern producers.4
It was early discovered that of all the available rocks in the
state only the Niagara dolomite produced a lime free enough of
impurities to satisfy the demands of the trade. Consequently,
the commercial lime industry became more and more concen¬
trated in the eastern part of the state, a shift well shown in the
series of maps in Figures 3 to 6. Of the 51 plants operating in
the state in 1911, 30 were burning Niagara dolomite. The others,
except one plant working a thin, high-calcium formation of
Ordovician limestone in LaFayette County, were producing only
2 Albert G. Ellis describes the homes of the French settlers in Green Bay upon his arrival
the morning of September 1, 1822, as “. . uniformly whitewashed with lime”: Ellis, Albert G.,
“Fifty-four Year’s Recollections of Men and Events in Wisconsin,” Collections of the State Hist.
Soc. of Wis., 7: 215, 1876.
3JL A. Horlick and Sons opened their plant at Racine in 1853. A second plant was con¬
structed by William Beswick on the Root River one and one-fourth miles from the center of Racine
in 1860. See Butterfield, C. W., The History of Racine and Kenosha Counties, Wisconsin , p. 469,
Chicago, 1879.
A lime plant located at the base of the escarpment at Gardiner (now Little Sturgeon) for
a period between 1854 and 1877 shipped out as much as a boatload of lime a week. See Holand,
Hjalmar R., History of Door County , Wisconsin, pp. 429-433, Chicago, 1917.
The Druecker quarry north of Port Washington is another of the early kilns from which lime
was shipped by lake.
4 In a state survey published by the Western Historical Company in its History of Washington
and Ozaukee Counties, Wisconsin, Chicago, 1881, it is stated (page 171) that 400,000 barrels of
lime were produced annually at that time from the Niagara formation. Pellon Kilns at Pewaukee
are credited with a production of 12,000 barrels weekly, which were shipped to Chicago, Grand
Haven and Des Moines.
In 1887 Wisconsin’s production was estimated at 1,000,000 barrels of lime (200 pounds per
barrel), while the national production was estimated to be 46,750,000 barrels {Mineral Resources
of the United States, U. S. Geol. Surv., 1887, p. 533). In 1888 the state’s production had risen
to 2,060,000 barrels, of a national total of 49,087,000. {Mineral Resources of the United States,
U. S. Geol. Surv., 1888, p. 554). If this last figure is a fairly accurate estimate of Wisconsin's
Bertrand — Survey of the Wisconsin Lime Industry 401
for local use.5 In 1940 the eleven producers were located in the
eastern part of the state. All but one, the Green Bay plant of the
Western Lime and Cement Company, which was importing lime¬
stone from Michigan, were burning Niagara dolomite.
Recent Trends
Two significant trends in the national lime industry are re¬
flected in the Wisconsin industry. The first is the gradual ab¬
sorption of the industry by big companies with capital sufficient
to meet the varied and increasing demands of the market. The
second is the decrease in the number of plants with an accom¬
panying increased output per plant. The number of plants in
operation in Wisconsin declined from 48 in 1906 to eleven in
1932. Production, however, remained fairly uniform, as shown
in Figure 1, until 1925. This was largely due to the fact that the
first kilns to be abandoned were the small local producers.
Paralleling the national trend, as small producers suspended
operation, an increasing nercentage of the Wisconsin lime indus¬
try passed into the control of a big company. By 1924 ten of the
25 operating plants were owned by the Western Lime and
m.
Figure 1. The graph shows the number of tons of lime sold annually from
1904 to 1940 by Wisconsin producers. The solid line indicates the total amount
of lime sold while the two broken lines show the amount sold for the specific
purposes indicated. Note that as the total production declined a smaller
percentage has been sold for building purposes.
production, more lime was produced in 1888 than has been produced in the state in any year since
annual reports were first published in 1904.
9 Mineral Resources of the United States, U. S. Geol. Surv., 1911, Pt. 2, p. 806.
402 Wisconsin Academy of Sciences , Arts and Letters
to
ZD
mo
nxi-
1135
lit®
Figure 2. The graph shows the percentage of the entire national production
of lime contributed by the leading states and Wisconsin. The widths of the
shaded areas represent the percentages of the respective areas.
Cement Company. Two plants were owned by the Standard Lime
and Stone Company and the Valders Lime and Stone Company.
The other eleven plants were owned by individual operators.6
Of the 18 operating plants in 1929, the Western Lime and Ce¬
ment Company owned eight. Two were operated by the Stand¬
ard Lime and Stone Company, and eight producers operated
single plants.7 In 1989 the Western Lime and Cement Company
operated seven plants, the Standard Lime and Stone Company
two, and individual owners the other three.
Lime Plants
Of the plants now operating all but the Green Bay plant are
located at points where a rail line passes near a rock outcrop or
at points where the overburden of glacial till is relatively thin.
Five of the plants are located at the base of the Niagara escarp¬
ment ; six are located on the dip slope of the cuesta.
The Rockwell Lime Company north of Manitowoc is the only
plant in which lime is burned in pot kilns. All others operate
shaft kilns. The more modern rotary kiln has never been used
to burn lime in the state, very likely because this type is least
6 Mineral Resources of the United States, U. S. Geol. Surv., 1924, Pt. 2, pp. 220-221.
7 Mineral Resources of the United States, U. S. Geol. Surv., 1929, Pt. 2, pp. 297-298.
Bertrand — Survey of the Wisconsin Lime Industry 403
Figure 3. After U. S. Geological Survey, Mineral Resources of the United
States, Pt. 2, 1911, Plate V.
efficient in the use of fuel,8 an important item of cost in the Wis¬
consin industry. Pot kilns are vertical shafts which may be
operated continuously but are usually fired by batches. This type
is charged with alternating layers of limestone and fuel, which
must be strong enough to support the load in the kiln. Largely
due to loss of heat in the cooling period between batches, this
•Moyer, Forest T., “Lime-fuel Ratios of Commercial Lime Plants in 1939,” U. S. Bur. of
Mines, Information Circular 7174, pp. 6-7, 1941.
404 Wisconsin Academy of Sciences , Arts and Letters
Figure 4. Material from U. S. Bureau of Mines, Mineral Resources of the
United States , Pt. 2, 1924, pp. 220-221.
type is rated less efficient in the use of wood fuel than the shaft
kilns.9
Shaft kilns are generally short, wide, vertical stacks lined
with refractory material enclosed by either a steel or stone
casing.10 Stone is fed into the kiln at the top by means of a
tramway and dump cars, and the lime is drawn off at the bottom.
9 Moyer, Forest T., op. tit., page 8.
10 For a description of this and other types of kilns see Bowles, Oliver, and Banks, D. M.,
“Lime,” U. S. Bur. of Mines, Information Circular, No. 6884R, pp. 39-41, 1941.
Bertrand — Survey of the Wisconsin Lime Industry 405
Figure 5. Material from U. S. Bureau of Mines, Mineral Resources of the
United States , Pt. 2, 1929, pp. 297-298.
The rock is preheated by escaping gases in the upper part of
the stack. As it slides down into the calcining chamber, it is con¬
verted to lime by hot gases and flame eminating from two or
more fire boxes located in openings in the sides near the bottom
of the kiln. The lime is withdrawn at four-hour intervals from
the cooling chamber at the bottom of the kiln. Shaft kilns are
operated continuously, halting only for occasional repairs.
The capacity and the number of kilns per plant vary widely.
The Eden and Brillion plants of the Western Lime and Cement
406 Wisconsin Academy of Sciences , Arts and Letters
Figure 6. Information obtained from the ofiice of the Wisconsin Geological
and Natural History Survey.
Company each have ten kilns, while the plants of the Mayville
White Lime Works and of John F. Groth and Son at Cedarburg
have but three kilns. Most of the plants in the state, whether
operating or not, have either four or five kilns. Production varies
from six to sixteen tons per kiln per day, the average being
about ten tons.11 Six plants were producing both lump lime and
hydrated lime in 1940. Wood is used as fuel by all plants but
u For details of individual plants as of 1924 and 1929 see the following: Mineral Resources
of tne United. States, 1924, U S. Geol. Surv., pt 2, pp. 220-221 ; Mineral Resources of the United
States, 1929, U. S. Geol. Surv., pt. 2, pp. 297-298.
Plate 1. A symbol of declining industry, this abandoned lime plant is
located just south of Grafton in southern Ozaukee County. It is one of
several to be found in eastern and southeastern Wisconsin.
Plate 2. This view of the Brillion plant of the Western Lime and Cement
Company shows the northernmost of the ten kilns. Immediately to the right
is the hydrating plant where the lump lime is crushed and the underburned
and overburned lime is removed. The lime is then slaked mechanically with
just enough water added to complete the process without producing a sticky
or pasty product. The quarry is located on the left beyond the waste pile.
Note the pile of cordwood.
Plate 3. This view of the quarries northwest of Valders shows the end of the
lime kilns immediately left of the road and the cluster of company houses
surrounding the plant.
Plate 4. The Green Bay plant of the Western Lime and Cement Company
located on the west bank of the Fox River. The piles of limestone shown on
the dock are shipped from Rock Port, Michigan. The coal comes from West
Virginia. Lacking an unloading bridge, the plant can receive cargo only from
self-unloading boats which are equipped with a giant boom with an endless
conveyor.
Bertrand— Survey of the Wisconsin Lime Industry 407
the Green Bay plant, which burns bituminous coal. Operations
vary according to the seasons, with little activity during the
winter. The number of men employed fluctuates accordingly,
the number of workers engaged by the industry at any one time
never being very large. The 1940 census reported an annual
average of 169 wage earners employed by the lime industry in
Wisconsin in 1939. As few as 137 were employed in January,
and the number rose only to 182 in July. From six to eighteen
men are employed at each plant with about half of the crew
working in the quarry.
The average lime plant consists of a battery of three or more
kilns, the lower portions of which are enclosed in a long shed.
A narrow guage tramway leads from the quarry to the runway
across the tops of the smoking stacks. In addition to the kilns,
each establishment consists of sheds, a warehouse, and in some
instances a hydrating plant. Piles of cordwood occupy the sur¬
rounding yard. The edge of the quarry is generally strewn with
piles of overburden and waste materials from the quarry and
the kilns. Much of it is overgrown with brush and tall weeds.
In each case a railroad spur extends to the plant. In most in¬
stances company houses occupied by workers have been built
adjacent to the plants.
Changing Market Demands
Changes in the market demand and in the consumption of
lime throughout the nation are shown in Figure 7. Most signifi-
Figure 7. The graph shows the total amount of lime sold by prodocers in the
the nation and the amounts sold to various types of consumers from 1915 to
1940. Taken from the U. S. Bureau of Mines, Minerals Year Book , Review of
1840 , p. 1214.
408 Wisconsin Academy of Sciences, Arts and Letters
cant for the Wisconsin industry is the marked decline in the
amount of lime sold for construction purposes, a use for which
the Wisconsin product is eminently suited. For the nation as a
whole, less lime has been sold annually for building purposes
since 1930 than was sold in any year beginning in 1906 with the
exception of 1918. As shown in Figure 1 the decline in the
amount of building lime sold by Wisconsin producers is even
more severe than for the nation as a whole. No one factor ex¬
plains this decrease in the demand for building lime. To a cer¬
tain extent the decline is a reflection of the economic collapse of
1929 and the depression which followed. Moreover, data gath¬
ered by Hatmaker shows that the Chicago area, Wisconsin's
chief market, suffered more than other districts in the nation in
terms of a general decline in building since 1929.12 Following
the gradual demise of the lumber industry several Wisconsin
cities remained in a state of economic stagnation for several
years until substitute industries developed. This was counter¬
acted throughout the state as a whole, however, by the abnormal
building boom that followed cessation of building during the
first World War.
It is noteworthy that the building activity encouraged by
government grants and loans in the late thirties had relatively
little effect on the demand for lime. This perhaps reflects the
competition that has been given lime in recent years by gypsum
in the preparation of plaster, which in turn competes with a
variety of wall boards. In general construction, too, lime has
had to compete with cement. Cut stone and mortar have been
replaced by concrete in the construction of foundations, piers,
abutments, and retaining walls. Lime, however, is finding an
increased use in waterproofing concrete.
The Niagara dolomite burned for lime in Wisconsin pro¬
duces a fine quality, high-magnesium lime, which is excellent for
construction purposes but which has only limited uses as chemi¬
cal and industrial lime. Tests conducted by the United States
Bureau of Standards and by the University of Wisconsin Engi¬
neering Experiment Station show that mortars produced with
high-magnesium lime have greater strength than those produced
12 Hatmaker, Paul, “Trade Trends in the Lime Industry,” U. S. Bur. of Mines, Report #/
Investigations, No. 3227, Figs. 7 and 9, and p. 7, 1934.
Bertrand — Survey of the Wisconsin Lime Industry 409
with a high-calcium lime.13 Other factors in preparing the mor¬
tar, however, are more important than the type of lime used in
determining the strength, and either type of lime produces a
sufficiently strong mortar for ordinary building purposes. High-
magnesium lime generally slakes more slowly and at a lower
temperature than high-calcium lime and therefore yields less
mortar. The mortar, however, is more plastic, and has a greater
sand carrying capacity. This higher plasticity makes it espe¬
cially well adapted for finishing plaster.14
Lime has long been used in the chemical and manufacturing
industries. As early as 1911 a list of 47 different industrial uses
of lime was published by the United States Geological Survey.15
Both the number of uses and the quantity of lime required have
greatly increased in recent years. Lime is widely used as a
chemical reagent, and enters directly into the manufacture of
many products. In the same period that the sale of building lime
has declined the amount of lime sold annually to chemical indus¬
tries has risen from slightly over 100,000 tons to approximately
1,000,000 tons. Lime sold to the paper industry has risen in
amount from 152,681 tons in 1907 to 566,818 tons in 1940.
There is a great variation in the kind of lime required in
each of the various industrial and chemical uses.16 Some de¬
mand hydrated lime, while others require quicklime. For some
processes either high-calcium or high-magnesium lime are equal¬
ly satisfactory; others specifically require one or the other. In
general, the use of high-magnesium lime in industry is rather
limited. It is used as a hardening agent in the manufacture of
soft rubber goods, in the production of some types of glass, and
in tanning certain types of leather. On the other hand, high-
calcium lime must be used for water purification and in the
manufacture of alkalis, bleaches, and calcium carbide. Dolomitic
13 Emley, W. E., and Young, S. E., “Strength of Lime Mortar,” Proc. Am. Soc. Test. Mat.,
14, Pt. 2: 339-358, 1914.
Baker, George J., “Wisconsin Magnesium Lime Mortars,” Univ. of Wis. Eng. Expr. Sta.,
Bulletin, Series No. 75, 39 pages, 1933.
14 Hatmaker, Paul, “Utilization of Dolomite and High-Magnesium Limestone,” U. S. Bur. of
Mines, Information Circular No. 6524, p. 7, 1931.
15 Mineral Resources of the United States, U. S. Geol. Surv., 1911, Pt. 2, p. 650.
18 Steidtmann, Edward, “Limestones and Marls of Wisconsin,” Wis. Geol. and Nat. Hist. Surv.,
Bull. 66: 103-118, 1924. Hatmaker, Paul, “Utilization of Dolomite and High-Magnesium Lime¬
stone,” op. cit., pp. 9-13, 1931. Bowles, Oliver, and Banks, D. M., op. cit., pp. 17-25. Bowles,
Oliver, and Jensen, Mabel S., “Limestone and Dolomite in the Chemical and Processing Industries,”
U. S. Bur. of Mines, Information Circular, 7169, pp. 6-15, 1941.
410 Wisconsin Academy of Sciences, Arts and Letters
lime is undesirable in the tanning of most leather, in the re¬
fining of sugar, in the manufacture of either sand-lime or re¬
fractory brick, in the production of paint and varnish, as a
hardening agent for hard rubber goods, and in the cyanide pro¬
cess for the recovery of gold and silver. High-calcium lime is
required as a flux in the basic open-hearth process of steel con¬
version and in the manufacture of glycerin, soap, and lubricat¬
ing greases.
The paper industry consumes large quantities of lime, and
since Wisconsin has long ranked high in the manufacture of
paper,17 it would appear that the lime industry possesses an im¬
portant nearby market.
High-magnesium lime is required by the industry for the
preparation of a very fine-grained pigment for coating paper.
Unfortunately, however, in only one of the processes by which
pulp is digested is a high-magnesium lime preferred. As a con¬
sequence, lime sold to the paper industry by Wisconsin producers
has never since exceeded the 16,997 tons in 1915, the first year
that reports for specific industries by states were published. In
the sulfite process wood chips are digested under high pressure
and temperature in a liquor made of sulfur dioxide and lime.
In this case a dolomitic lime is preferred, for it is claimed that a
magnesium-bisulfite liquor is more soluble, more stable, and pro¬
duces a softer and whiter pulp than calcium bisulfite. In both
the soda process and the sulfate process of pulp production a
lime containing less than two per cent magnesia is used as caus-
ticizing agent in recovering the caustic soda and the sodium sul¬
fate respectively from the wash in which the pulp has been
digested.18 In the Jennsen tower system, however, a high-calcium
limestone rather than lime is used. Methods are steadily being
improved by which lime can be recovered and used again thus
cutting down the total demand for lime by the paper industry.
In answer to the demand for high-calcium lime the Western
Lime and Cement Company in 1923 constructed a plant consist¬
ing of five shaft kilns on the west bank of the Fox River in Green
Bay. From the beginning of operation a high-calcium limestone
17 Ranked third after Washington and Maine in both tons of pulp produced and cords of pulp-
wood consumed in 1939. Census of Manufactures, 1939, 16th Census of the United States.
38 Bowles, Oliver, and Banks, D. M., op. cit., pp. 19-20.
Bertrand — Survey of the Wisconsin Lime Industry 411
has been shipped by boat from eastern Michigan.19 At the pres¬
ent, bituminous coal from West Virginia is also shipped by
water. The plant has a capacity of 30 tons of lime daily, but in
1940 was operating only at 60 per cent capacity. At least 50 per
cent of the output which is high-calcium lime is sold as chemical
lime with a higher percentage in winter when operations are cut.
About 25 per cent of the output in spring is sold as agricultural
lime.
That the Wisconsin industry is failing to meet the demands
even within the state is revealed by statistics for recent years
which show that the consumption of lime in Wisconsin has ex¬
ceeded production each year since 1930. In that period produc¬
tion has ranked from 44 to 66 per cent of consumption, being
over 60 per cent for five years and under 50 per cent for two.
Due to the fact that Wisconsin has continued to ship high quality
lime to other states the actual proportion of Wisconsin-produced
lime consumed within the state is even smaller. The deficit be¬
tween Wisconsin lime consumed in the state and total consump¬
tion is made up by shipments from other states. These imports
have since 1930 been nearly equal to and in some cases have ex¬
ceeded Wisconsin production.
From the foregoing discussion it is apparent that the Wis¬
consin lime industry is greatly restricted in a market demanding
high-calcium lime while it produces mainly high-magnesium
lime. This fact in itself, however, is not the sole reason for the
decline of the industry, for the greatest share of the lime pro¬
duced in Ohio, the leading producer, is dolomitic lime. More¬
over, the Ohio production has steadily increased and now totals
25 per cent of the nation's output.
Annual statistics from 1915 to 1932 show that as in Wis¬
consin, over 50 per cent of the Ohio production was sold to the
construction industry. Since then the proportion of the lime
sold for building purposes in both states has dropped below half
of the total. In general, however, a greater proportion of the
Ohio production has always been sold for non-building uses than
has been true for Wisconsin. It is significant that even in the
amount of lime sold to the paper industry, Ohio exceeds Wiseon-
19 For a discussion of the Michigan limestone industry see Morrison, Paul C„, “Michigan Lime¬
stone Industry,” Ecott. Geog., 18: 2S8-2 74, 1942.
412 Wisconsin Academy of Sciences , Arts and Letters
sin by a considerable tonnage in spite of the fact that it is un¬
important in paper production. The superior status of the Ohio
lime industry, concentrated in the northwestern part of the
state, can be explained in part by its more central location
within the great northeastern industrial quadrant of the nation,
thereby having an advantage in transportation costs. However,
as has been shown, the Wisconsin industry is no longer meeting
the demand for lime within the state itself, where transportation
costs would be in its favor. An important advantage in favor of
Ohio is the cost of fuel.
Fuel
With few exceptions, where producer gas and coal were ex¬
perimented with, wood has been the main fuel used by the Wis¬
consin lime industry, and at present all but the Green Bay
plant still use wood. Formerly this fuel was cheap and locally
abundant. At present it is largely shipped in by rail from the
cutover region of the Upper Lakes. Wisconsin producers claim
that it costs about 75 cents more to produce a ton of lime with
wood than with coal, but that if high-magnesium lime is to be
used by the paper industry it must be burned with wood. This
is perhaps due to the fact that lime can be burned more steadily
and at a lower temperature with wood than with coal. The mini¬
mum temperature of the decomposition of dolomite is lowered by
the steam released as one of the gases of combustion in the burn¬
ing of wood. As a result of this lower temperature the impuri¬
ties are less active, thus making a purer lime, an important
factor in the paper industry.
The depletion of the former abundant supply of cordwood is
an important factor in the ability of the Wisconsin lime pro¬
ducers to compete with producers in other regions, particularly
Ohio, Pennsylvania, West Virginia, and Missouri, all of which
lie within, or relatively near, coal fields. Since the average price
of a ton of lime ranges between six and eight dollars, it is obvi¬
ous that a slight difference in the comparative cost of fuel used
to produce that lime will greatly affect the ability of the producer
to compete on the national market. Comparison with Ohio is
perhaps justified, since it too produces mainly high-magnesium
lime. All other major producing states specialize in high-calcium
lime. Compared to fuel costs in Ohio, the additional freight in-
Bertrand — Survey of the Wisconsin Lime Industry 413
volved in shipping coal from West Virginia, Pennsylvania, or
Ohio to Wisconsin lime kilns is of consequence. That it is done
at all is due to the cheap water transportation available to the
Green Bay plant. But in this one instance high-calcium lime¬
stone is also imported. Furthermore, Green Bay is located in one
of the major paper-making regions of the state. Few localities in
the state can boast this combination of advantageous factors.
Fuel costs vary with individual plants making a general com¬
parative figure difficult to obtain. It would appear, however,
that fuel costs per ton of lime are between 60 and 75 cents great¬
er in Wisconsin than in Ohio. This reflects particularly the in¬
creasing difficulty in obtaining adequate and inexpensive sup¬
plies of cordwood in Wisconsin.
Conclusion
Within the past fifteen years the Wisconsin lime industry has
experienced a remarkable decline, resulting from a combination
of factors, three of which appear to be most important. First,
the industry is suffering from a decline in the demand for con¬
struction lime, a use for which the Wisconsin product is best
suited. Secondly, the industry is unable to meet the demand for
lime by chemical and manufacturing industries because Wis¬
consin's high-magnesium lime is not well suited for that pur¬
pose. Thirdly, Wisconsin producers are at a competitive disad¬
vantage due to the comparatively high cost of fuel as the supply
of cordwood has become depleted. Hope for the future lies main¬
ly in cheap labor, in supplying nearby markets, and in new tech¬
nological developments. Perhaps of greatest interest for the
Wisconsin industry are recent experiments in obtaining prac¬
tically complete hydration of the magnesia in dolomitic limes
when hydration is conducted under pressure.
STUDIES OF SILURIAN FOSSILS IN THE
THOMAS A. GREENE COLLECTION AT
MILWAUKEE-DOWNER COLLEGE
Katherine F. Greacen and John R. Ball
The Thomas A. Greene Memorial Museum was established at
Milwaukee-Downer College in 1913, the gift of the heirs of the
collector. The mineral collection has been catalogued, but the
fossil collection is so extensive that it has never been completely
studied nor catalogued.
Thomas A. Greene was born in Providence, Rhode Island, in
1827. While still in grade school, he became interested in the
study of geology and botany, and began collecting Rhode Island
minerals, thus forming the nucleus of the present extensive
geological collection. At the age of sixteen, young Greene went
to work in a drugstore. Deciding to make this his life work, four
years later he set out for the west, seeking a new home and his
fortune. He arrived in Milwaukee July 4, 1848. Finding a drug¬
store for sale in Milwaukee, he bought it, and sent for his friend
Henry H. Button. The firm of Greene and Button later gave up
the retail drug business, and became a prosperous wholesale
house.
The pressure of a growing business concern did not leave
Greene much time for his hobbies ; but the fact that he made his
buying and selling trips in the summer, leaving winter travel to
his partner Button, indicates that he may have made side trips
to study geology and botany, as he did on his trip west at the age
of twenty. By 1857, apparently the business was successful
enough to permit Greene to go back to his mineral collection, and
to enlarge and improve it, chiefly by purchases from dealers.
When his health failed in 1878, and his physician advised
him to give up work for a while and spend as much time as pos¬
sible outdoors, Greene turned, naturally, to examining the rocks
in the vicinity of Milwaukee. These did not yield many minerals,
but they were full of fossil forms.
It was not long before his interest was centered wholeheart¬
edly on the collection of these fossils, and Greene, a perfection-
415
416 Wisconsin Academy of Sciences, Arts and Letters
ist, set himself the task of building up as complete and perfect
a fossil collection as he could. The circumstances were peculiarly
favorable for such a purpose — Greene had the time to visit quar¬
ries, examine and study specimens, make exchanges and carry
on an extensive correspondence. He had plenty of money to
spend on fossils — he outbid the Public Museum on certain occa¬
sions, and made a practice of paying quarrymen in advance, to
reserve the best specimens for himself ; and it was a time when
many new quarries were being opened. Through the 1880’s and
early 1890’s, when he was collecting most actively, quarries were
being worked which are no longer available, and Greene was able
to obtain excellent specimens from the upper horizons as well as
from the lower ones.
As Greene stressed in his letters concerning exchanges, the
emphasis was on quality, not quantity. The quantity rose, how¬
ever, to an estimated total of 65,000 to 75,000 specimens. The
Silurian and Devonian fossils are by far the most abundant,
since they are the ones which occur in and around Milwaukee.
Greene determined to make his Silurian collection as complete
as possible, and so, after scouring the quarries of Wisconsin and
Illinois, he visited the famous locality at Waldron, Indiana, and
also acquired some specimens from Niagara County, New York
and Hardeman County, Texas. As the Silurian and Devonian
collections grew, Greene began to collect fossils from all the
other geological periods, acquiring some by personal field trips,
but completing the collection chiefly by purchase and exchange.
Greene loved nothing better than to get to the quarries him¬
self, and his correspondence shows that he frequently made such
trips, usually writing to the quarrymen in advance, so that they
would have an array of their finds ready for him to inspect. He
was a busy man, however, and so he had to rely more and more
on exchanges and purchases for his new specimens, rather than
on collecting trips. He was very particular and meticulous in all
his dealings. In general, he seems to have preferred to purchase
material, rather than to obtain it by exchange. When he did
make an exchange, he sent only the best material, and demanded
similar quality in the specimens sent to him. After unsatisfac¬
tory dealings with certain men, he refused to examine any more
of their material, complaining that it would be a waste of time.
Their boxes were returned, unopened.
Greacen and Ball — Silurian Fossils in Greene Collection 417
Because of his interest in the fossils, Greene trained himself
to be a thoroughly competent paleontologist. He read a great
deal, and studied his acquisitions carefully, labeling many of
them quite completely. Others, however, were left unclassified.
Greene did not hesitate to call on the leading paleontologists of
the day when he was at a loss to identify his specimens, nor when
he found something unusual. The labels contain notations by
James Hall, Charles Wachsmuth and Robert P. Whitfield.
Greene's notes indicate that from time to time these men sug¬
gested that probably he had new species in his collection. These
suggestions have been noted in the present study, but there has
not been time as yet to verify or disagree with them. In some
cases, new species of brachiopods actually were described by
James Hall. Some of these were named after Greene, an honor
which pleased him highly.
Except for a preliminary study of the type specimens in the
collection, the present work has been confined to Niagaran fos¬
sils from Illinois — almost entirely from Cook County. They are
from quarries at Bridgeport, Cheltenham, Cicero, Hawthorne,
Lyons and Stony Island. Practically all of these localities now
are inaccessible to collectors. The collections include, altogether,
more than 7,400 specimens which have been examined and listed
by the authors. Many of the identifications are tentative, how¬
ever, and more thorough work is necessary before the classifica¬
tion can be considered final. It is highly probable that there are
new species in the material that has been studied, but final judg¬
ment is withheld. The greatest number of new species probably
will be described from the Crinoidea; others will be from the
Cystoidea; and probably a few Mollusca, Brachiopoda and An-
thozoa. It is fortunate that the probable new species are repre¬
sented by a large number of specimens in most cases, and it is
hoped that the same forms may be found in other collections.
Aside from the finding of new species, the work has been
very interesting because of the wide variety of species repre¬
sented, and the excellence of the material. Some forms are ex¬
tremely abundant ; others are labeled “rare" and are represented
by relatively few specimens. In some cases, where certain spe¬
cies never before described from Cook County have been found,
new evidence of the faunal population of Silurian seaways may
be inferred.
418 Wisconsin Academy of Sciences, Arts and Letters
The compilation of species has not been completed, but an
idea can be given of the generic range in the Niagaran rocks of
Cook County. Porifera are relatively scarce, and are represented
by two or three genera — Ischadites, Receptaculites , and an un¬
determined “rare” form. Corals are much more abundant, and
are represented by at least 16 genera. Both solitary and colonial
forms are present. Bryozoa are chiefly of the fenestellid group,
but there are a few others. Brachiopods are present in great
abundance, with at least 29 genera, representing both the In-
articulata and the Articulata. There are good representations of
internal spiralia, as well as the more common features. The
Echinoderma are also extremely well represented. There are at
least 5 cystoid genera, 1 or more blastoids, and 20 or more gen¬
era of crinoids, representing a large number of species. Mol-
lusca are represented by large and small Pelecypoda, Gastropoda
and Cephalopoda, involving at least 9, 18, and 13 genera respec¬
tively. The Arthropoda are represented by about 15 genera of
trilobites, of which Bumastus is the most abundant.
Further studies probably will reveal additional genera. There
is no doubt that the number of species is large, and the abun¬
dance of specimens permits comparisons which may yield inter¬
esting results.
Genera Represented in Niagaran Material from Cook County, Illinois
( List is tentative and incomplete.)
Sponges
Receptaculites
Ischadites
Cerionites
Corals
Zaphrentis
Amplexus
Streptelasma
Diphyphyllum
Omphyma
Chonophyllum
Strombodes-
Arachnophyllum
Cystiphyllum
Cystiphorolites
Heliolites
Favosites
Alveolites
Cladopora-
Coenites
Syringopora
Halysites
Stromatopora
Cystoids
Holocystites
Caryocrinites
Hallicystis
Coelocystis
Gomphocystites
Blastoid
Troosticrinus
Crinoids
Dimerocrinus
Cyphocrinus
Gazacrinus
Lampterocrinus
Siphonocrinus
Archaeocrinus
Lyriocrinus
Melocrinus
Macrostylocrinus
Eucalyptocrinus
Calliocrinus
Periechocrinus
Platycrinus
Lecanocrinus
Icthyocrinus
Stephanocrinus
Crotalocrinus
Cyathocrinus
Bryozoans
Ceramopora
Fenestella
Undetermined
Brachiopods
Monomorella
Trimerella
Orthis
Leptaena
Stropheodonta
Strophonella
Schucherteila
Triplecia
Greacen and Ball — Silurian Fossils in Greene Collection 419
Parastrophia
Anastrophia
Conchidium
Strieklandinia
Pentamerus
Clorinda
Gypidula
Sieberella
Rhynchotreta
Uncinulus
Wilsonia
Camarotoechia
Rhynchotrema
Magellania
(Waldheimia)
Atrypa
Spirifer
Cyrtia
Homoeospira
Whitfieldia
Nucleospira
Meristina
Pelecypods
Cleidophorus
Edmondia
Cypricardites (?)
Pterinea
Ambonychia
Amphicoelia
Conocardium
Modiolopsis
Cypricardinia
Gastropods
Sinuites (?)
Tremanotus
Pleurotomaria
Phanerotrema
Murchisonia
Straparolus
Euomphalus
Raphistoma
Euomphalopterus
Trochonema
Cyclonema
Strophostylus
Holopea
Loxonema
Subulites
Cyrtospira
Platyceras
Diaphorostoma
Cephalopods
Orthoceras
Dawsonoceras
Protokionoceras
Kionoceras
Lituites ??
Gyroceras
Trochoceras
Actinoceras
Cyrtorizoceras
Cyrtoceras
Protophragmoceras
Gomphoceras
Phragmoceras
Trilobites
Illaenus
Illaenoides
Scutellum
Goldius
Lichas
Metapolichas
Arctinurus
Dicranopeltis
Ceratocephala
Encrinurus
Calymene
Cheirurus
Sphaerexochus
Dalmanites
BORON DEFICIENCY IN BEETS AS CORRELATED WITH
YIELDS AND AVAILABLE BORON1
K. C. Berger and E. Truog
Department of Soils, University of Wisconsin
Introduction
Boron is now known to be one of the 15 essential nutrient
elements required by higher plants. Although Wittstein and
Apoiger (10) in 1857 found boron in the ash of the seed of
Maesa picta, it was not until 1915 that Maze (6) demonstrated
that boron is essential for the normal growth of the corn plant.
In 1910 Agulhon (1) obtained increased yields of wheat, oats,
and turnips by the use of boron in nutrient solutions, but he did
not establish the essentiality of boron for the normal growth of
the plants. In 1923, Warrington (9) showed that boron is essen¬
tial to legumes and that its absence causes distinct deficiency
symptoms.
Brandenburg (5) in 1931 discovered that the application of
boron prevents heart rot of sugar beets, and in 1938 Raleigh and
Raymond (7) found that fertilization with boron would control
internal breakdown of table beets. Also, in 1938, Walker, Joli-
vette, and McLean (8) published their findings which showed
that boron is essential for the normal growth of table beets, and
that a lack of the element causes deficiency symptoms which
they called black spot instead of internal breakdown or rot.
The amounts of boron normally present in various plants
expressed in parts per million of the dry tissue are as follows :
barley, wheat, and corn, three to 10 parts ; spinach, celery, and
peas 10 to 20 parts; carrot and red clover 20 to 30 parts; and
cabbage, alfalfa, turnips, tomato, sugar beet and table beet
30 to 50 parts. Plants containing the higher amounts of boron
also require greater amounts of available boron for normal
growth.
The boron content of soils varies considerably even though
the amounts normally present in soils of the humid temperate
‘This work was given financial aid by the American Potash Institute, Inc., and publication is
approved by the Director of the Wisconsin Agricultural Experiment Station.
421
422 Wisconsin Academy of Sciences , Arts and Letters
regions are relatively low. Sands usually contain from two to
10 parts per million of total boron and loams 15 to 40. Ordi¬
narily, about five per cent of the total boron present is available ;
thus, sands and soils low in organic matter and also calcareous
soils usually contain from 0.1 to 0.7 part per million of available
boron, while slightly acid soils, high in organic matter, usually
contain from 0.7 to 4.5 parts per million.
Methods involving the quinalizarian reaction for the deter¬
mination of total boron in soils and plants, and available boron in
soils have been developed and described by the writers (2),
(3), (4). Treatments of soils with boiling water was found to
be the most satisfactory procedure for the extraction of avail¬
able boron, and hence, this means was adopted. The results ob¬
tained for available boron with this method were correlated with
the boron deficiency symptoms found in table beets and a good
correlation was obtained (3).
Visual deficiency symptoms are usually found only when the
deficiency becomes rather extreme, and thus slight deficiencies
go unnoticed, although yields may be appreciably lowered. In
order to obtain additional information regarding boron defi¬
ciency symptoms in beets as correlated with yields and the avail¬
able boron content of soils, further investigations were con¬
ducted. A brief discussion of these and the results obtained
follow.
Experimental
During a four-year period, field fertilizer experiments were
conducted with beets in eastern Wisconsin on three soil types.
Each of these experiments involved numerous plots variously
treated with the common fertilizers, and in addition some of the
plots also received borax. Only data obtained from a set of plots
which received a 3-12-12 fertilizer alone, and another set which
received borax in addition are presented here (Table I).
The data given in Table I for the available boron content of
the soils represent the average of results obtained by analyzing
a sample of soil from each plot before treatment. The plots on
each soil type were found to be very uniform as regards the
available boron content of the soil, the greatest variation being
± 0.15 part per million of boron.
The data given for yields represent an average of four ran¬
domized replicated plots; each plot was four rows wide and 70
with and without boron fertilization.
Berger and Truog - — Boron Deficiency in Beets
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423
424 Wisconsin Academy of Sciences , Arts and Letters
feet long. For obtaining yields, the inner two rows, 60 feet long,
were harvested. Boron deficiency symptoms were noted by visual
observation of the tops throughout the growing season, and by
examination of the roots at harvest.
Discussion
When soil tests for available boron were correlated with
boron deficiency symptoms in table beets in a previous investi¬
gation (3), it was found that when the soil contained about 0.76
part per million of available boron the boron deficiency symp¬
toms were reduced to a negligible degree. However, in the case
of most nutrient elements, even before deficiency symptoms ap¬
pear, the yield is lowered by a slight deficiency of one of these
elements. The results given in Table I show that this holds true
for boron in the case of beets. The results also show that sugar
beets require at least about one part per million of available
boron in soils rather than 0.75 part as previously stated. Table
beets probably require slightly more.
The response to applications of borax is greatly influenced by
the moisture conditions during the growing season; in 1940, a
wet growing season, the increase in yield of table beets was only
15 per cent when borax was applied to a soil having 0.5 part per
million of available boron, while in 1943, a dry growing season,
the increase in yield was about 31 per cent when borax was
applied to a soil having 0.9 part per million of available boron.
The level of available nutrients other than boron is also a
factor in determining the amount of available boron needed by
the crop. In 1941, on a highly fertile Miami silt loam having
0.8 part per million of available boron, a 24-per cent increase in
yield was obtained by the application of borax, and 30 per cent
of the beets where borax was not applied had visual boron de¬
ficiency symptoms. The yield was greater than in 1940 on this
same type of soil, and a greater response to borax was obtained
because of larger plant growth due to higher fertility, and con¬
sequently a larger demand for boron.
Summary
Since boron deficiency symptoms in beets appear only when
the deficiency becomes quite serious and after yields are mark¬
edly reduced, such symptoms do not always serve as a satisfac¬
tory means of telling when fertilization with boron is needed.
Berger and Truog— Boron Deficiency in Beets 425
Determination of available boron in soils, involving extraction
with hot water, appears to be a much more satisfactory means
of doing this. Results from field tests indicate that sugar beets
require at least about 1.0 part per million of available boron, and
table beets slightly more. Common field crops probably require
less than one-half these amounts.
Literature Cited
(1) Agulhon, H.
1910. Emploi du bore comme engrais catalytique. Compt. rend., 150:
288-291.
(2) Berger, K. C., and Truog, E.
1939. Boron determination in soils and plants using the quinalizarin
reaction. Ind. Eng. Chem., Anal. Ed., 11: 540-545.
(3) Berger, K. C., and Truog, E.
1940. Boron deficiencies as revealed by plant and soil tests. J. Amer.
Soc. Agron., 32: 297-301.
(4) Berger, K. C., and Truog, E.
1944. Boron tests and determinations for soils and plants. Soil Sci.,
57: 25-36.
(5) Brandenburg, E.
1931. Die Herz-und Trockenfaule der Riiben als Bormangel-Erschei-
nung. Phytopath. Zeits., 3:499-517.
(6) Maze, P.
1915. Determination des elements mineraux rares necessaires au de-
veloppement du max's. Compt. Rend. Sci., 160: 211-214.
(7) Raleigh, G. J., and Raymond, C. B.
1938. A preliminary note on the control of internal breakdown in
table beets by the use of boron. Proc. Amer. Soc. Hort. Sci., 35: 526-
529.
(8) Walker, J. C., Jolivette, J. P., and McLean, J. G.
1938. Internal black spot of canning beets and its control. Canning
Age, Dec. 1938.
(9) Warrington, K.
1923. The effect of boric acid and borax on the broad bean and certain
other plants. Ann. Bot. (London), 37: 629-672.
(10) Wittstein, A., and Apoiger, F.
1857. Entdeckung der Borsaure im Pflanzenreiche. Ann. Chemie
Pharm. (Liebig), 103: 362-364.
THE ACIDITY OF HONEY*
H. A. SCHUETTE AND FRANK J. SCHUBERT
Department of Chemistry , University of Wisconsin
“Honey is nothing else but a Composition of an infinite Num¬
ber of Flowers, which the Bees suck and receive into their Stom¬
achs, Carry into their Hive, and afterwards disgorge into small
square Holes made of Wax, and prepared by them before, where¬
in they keep Honey for their own Nourishment.” This two-cen¬
tury-old definition (Lemery-1745) has been superseded by its
modern, official one: the nectar and saccharine exudation of
plants gathered, modified and stored in the comb by the honey¬
bee. This modification of nectar and saccharine exudation re¬
sults in the production of an unrefined, concentrated syrup of
invert sugar having a flavor which is characteristic of its floral
source.
Among the minor components of honey there are a consid¬
erable number of mineral constituents, esters and other volatile
compounds, organic acids, proteins, amino acids and substances
closely related to them, plant pigments, seven members of the B
vitamin complex, ascorbic acid and dextrins. Very largely re¬
sponsible for the differences in the taste characteristics of the
different floral types of honey are the first three of this group.
Several reports on the nature and the identity of the acids in
honey have been made by those who have studied this problem,
the most convincing evidence yet presented being that of Nelson
and Mottern (1931) whose investigations covered 15 honeys of
different floral types. Formic acid was found in all of them but
in amounts so small as hardly to justify the assumption of the
importance which had hitherto been given it. The largest amount
of this acid, or .024 per cent, was found in tulip honey. The
acetic acid content, in the group studied, reached its highest
concentration, or .046 per cent, in sage honey. Succinic acid was
identified in sourwood, cotton blossom and tulip honeys, and in
all of them citric and malic acids. Because the latter are widely
* Published here by permission of Industrial and Engineering Chemistry.
427
428 Wisconsin Academy of Sciences , Arts and Letters
distributed in fruits and other plant materials, their presence in
honey is to be expected. Heiduschka (1911) found oxalic acid
in several honeys, an observation which is not necessarily unique
in view of the known occurrence of calcium oxalate in the vege¬
table kingdom.
Normal, natural honey has an acid reaction, a condition to
which its volatile acids and the acid salts of its non-volatile ones
are contributive. The actual quantity of these acidic constitu¬
ents, or titratable acidity, has been determined by various in¬
vestigators and has been found to be of the order of magnitude
of 4 cc. of N alkali solution per 100 g. of honey. Fermentations
of the acetic or lactic acid types and similar agencies cause an
appreciable increase in its natural acidity. Unripe honeys fre¬
quently show lower values.
The intensity or degree of this acidity is, however, another
matter; it is expressed as hydrogen ion concentration in terms
of the so-called pH scale. Contributive to this degree of acidity
is not only the total amount and nature of the acids present but
also, among others, the mineral constituents.
Published information on the hydrogen ion concentration of
honey is not extensive. With one known exception it is of for¬
eign origin. The reports of Fiehe and Kordatzki (1928) who
surmised that the hydrogen ion concentration of a honey is an
index of either a natural or a synthetic past, of Elser (1929), of
Stitz and Szonntag (1932) and of Canned and Salani (1935)
reveal a variation in the pH of this food between 3.29 and 4.87.
The few values reported by Bridges and Mattice (1938) for the
American-grown product lies within these limits.
Quite apart from the value of conducting a fact-finding sur¬
vey as to the pH of domestic honeys in comparison with those
grown in Europe, or of securing data for use as a helpful tool
in gathering proof of alleged honey adulterations — this is appar¬
ently no longer a serious problem in this country — lies a very
practical interest in the application of these data to industrial
problems. The situation in question is one now confronting man¬
ufacturers of confectionery who share with the housewife the
obligation of conserving the nation's sugar supplies. At least
one instance is known in which factory batches of confectionery,
wherein honey had been substituted wholly or in part for su¬
crose, failed the laboratory formula because it had been assumed,
apparently, that the pH of this natural sweet is a constant fac¬
tor.
Schuette and Schubert — The Acidity of Honey 429
Experimental
Available for this survey was a group of 48 samples which
on other occasions had been used in this laboratory in a series of
studies on the chemistry of honey. Among them were repre¬
sentatives of the whole gamut of the color classification used in
the merchandizing of honey (Sechrist — 1925), from the so-called
water-white to dark. Geographically, they represent a wide dis¬
tribution. With few exceptions, and these were bottled blends for
the retail trade, they had been obtained from the growers them¬
selves in Arkansas, California, Colorado, Florida, Georgia, Illi¬
nois, Minnesota, New York, Ohio, South Carolina, Texas, Vir¬
ginia, West Virginia, Wisconsin, Hawaiian Islands, Panama and
West Indies. Included herein were honeys whose known pre¬
dominant floral sources were, respectively, alfalfa, algarroba,
blue curls, buckwheat, several varieties of clover, cotton blos¬
som, gallberry, holly blossom, horsemint, mesquite, orange blos¬
som, pepper bush, white sage, sourwood, spike weed, tamarisk,
thistle, titi, tupelo, tulip poplar and wild flowers.
Approximately one third of this lot had been received in the
comb. The extracted variety included 14 honeys packaged in
glass jars and 17 in tinned containers. Seven chunk comb hon¬
eys are included in the latter group. Their contact with tin could
not have been long. The comb honeys were strained through
cheesecloth and all samples were stored in glass while awaiting
analysis.
Earlier investigators in this field had used the colorimetric
method with a series of indicators for determining the hydrogen
ion concentration of honey. This method, however, cannot be
recommended for general use, and probably not in this instance,
because of the errors introduced by proteins, salts, the color of
the material under examination, oxidation-reduction systems and
the temperature coefficient. Others reported having used an
electrometric technique.
With the introduction of the portable pH meter, its electrode
assembly and other appurtenances in compact form, these meas¬
urements can now be readily made. Two of the standard com¬
mercial forms, the Beckman and the Coleman, were used in this
investigation.
Ash determinations were made in platinum dishes at tem¬
peratures well below the volatilizing temperatures of the in¬
organic constituents of honey.
430 Wisconsin Academy of Sciences , Arts and Letters
Results
All data have been more or less arbitrarily grouped into two
divisions (Tables I and II), light and dark, as typifying in a
qualitative sense the most obvious color-differences. This sep¬
aration is consistent with the present merchandizing practice
inasmuch as a statement of floral source is not a condition in-
Table I. Hydrogen ion concentration of light honeys.
volved in the lawful, interstate sale of honey. By this scheme of
division, the light-honey group includes those whose predominat¬
ing floral sources are alfalfa, algarroba, several species of clover,
orange blossom and white sage, respectively. Similarly, the mem¬
bers of the dark-honey group had their origins in buckwheat,
holly blossom, Mexican clover, pepper bush, sourwood, spike
weed, tamarisk, thistle and titi (buckwheat tree). These data
have been grouped (Table III) also to show the relationship
Schuette and Schubert — The Acidity of Honey
431
Table II. Hydrogen ion concentration of dark honeys.
which was revealed here between the color grade of the honeys
and their respective hydrogen ion concentrations.
Summary
The pH of all samples studied lay between 3.16 and 4.52,
values which are of the order of magnitude of those reported by
European workers, or 3.29 and 4.87. Geographical origins ap¬
parently exert little influence on this value. If the pH values
herein reported be converted into their corresponding hydrogen
ion concentrations — they then become mathematical expressions
— an average of 3.59 results. This average for the whole group
432 Wisconsin Academy of Sciences , Arts and Letters
Table III. Color grade of honey in relation to its hydrogen ion concentration.
* For purposes of comparison, these values have been treated as if they were
actual numbers when in fact they are logarithmic. However, for practical
purposes no serious error has been committed in this instance in reporting an
arithmetic mean because of the fact that the pH values here lie within a
narrow range.
is in good agreement with that reported by Bridges and Mattice
(1938), or 3.8, who contrasted their value with that of maple
syrup, or 5.5, and a popular brand of so-called corn syrup, or
4.5.
Although the data herein presented have not been segregated
according to type of honey examined, it may be stated that the
comb honeys had a lower pH (3.52) than extracted honeys pack¬
aged in glass or in tin containers. The extracted honeys which
had been received in glass containers had practically the same
pH as those packaged in tinned containers, the average pH
values for the extracted honeys being 3.62 and 3.61, respectively.
The per cent of ash was found to vary over a wide range;
in general an increase in ash accompanied an increase in pH
and an increase in color.
Literature Cited
Bridges, M. A., and M. R. Mattice.
1938. Over two thousand estimations of the pH of representative
foods. Am. J. Dig. Dis. Nutrit., 6:440-449.
Canneri, G., and R. Salani
1935. The composition of Italian honeys ( trans . title). Ann. chim.
applicata, 25:397-406; Chem. Zentr., 1936 1:2850.
Elser, E.
1929. Die Grundlagen der Chemischen Honigforschung. XII. Die
Methodik der chemischen Untersuchung des Honigs. Landw. Jahrb.
Schweiz, 43:471-499.
Schuette and Schubert — The Acidity of Honey 438
Fiehe, J., and W. Kordatzki,
1928. Ueber der Sauregrad (die Wasserstoffkonzentration) von Honig
und Kunsthonig. Ztschr. Untersuch. Lebensm., 55:59-63.
Heiduschka, A.
1911. Ueber die Sauren im Honig. Pharm. Zentralhalle, 52:1051-1053.
Lemery, L.
1745. A Treatise of all Sorts of Foods, both Animal and Vegetable:
also of Drinkables. London. 3 ed. p. 263.
Melson, F. K., and H. H. Mottem
1931. Some organic acids in honey. Ind. Eng. Chem., 23:335-336.
Sechrist, E. L.
1925. The color grading of honey. U. S. Dept. Agr. Circ. 364, 5.
Sfcitz, J., and J. Szonntag,
Der Wasserstoffionenkonzentration des Honigs. Ztschr. Untersuch.
Lebensm., 63:215-218.
I
'
.
I
GASOGENS
C. V. Sweet
Chief, Division of Industrial Investigations
Forest Products Laboratory* , Forest Service
U. S. Department of Agriculture
The gasification of wood or charcoal in generators, com¬
monly called gasogens, attached to trucks, busses, passenger cars,
tractors, and motor boats for use in lieu of gasoline has been
developed vigorously during recent years in several foreign
countries. It is applicable for use with internal combustion en¬
gines other than diesels. Probably the most active development
since the start of the war has taken place in Sweden and in
Germany. In countries where the gasoline supply has seemed
to be adequate, the interest in substitute fuels, especially non¬
liquid fuels, has been relatively small. Of 74,567 motor vehicles
registered as operating in Sweden in 1942, over 90 per cent were
operated by means of gasogens. Some reported figures as to use
of gasogens in other countries are as follows :
A few experimental units have been operated in Canada and
the United States.
Thus the term “gasogen” is more familiar to audiences in
many foreign countries than in the United States. Under nor¬
mal conditions, wide-spread commercial adoption of gasogens,
or producer-gas units, is certainly not to be expected. Under
certain conditions such that large quantities of gasoline are used
for long steady hauls, especially in wooded or farm woodland
areas, it is not impossible that sufficient saving in fuel costs can
be realized to compensate for the disadvantages that lie in a non-
liquid fuel. Use on Wisconsin farm tractors seems quite remote
at present due to interference with the vision of the operator
* Maintained at Madison, Wis., in cooperation with the University of Wisconsin.
435
436 Wisconsin Academy of Sciences , Arts and Letters
and interference with maneuverability. Wisconsin's portable
sawmills may come to use them ; so may some other similar users
of gasoline.
The Forest Products Laboratory undertook a limited amount
of active work on the subject of gasogens in 1943 after follow¬
ing, by remote control for several years, the developments in
European countries. The Laboratory undertook active work be¬
cause Chinese supply officials in Washington were anxious to
have built and tested a unit of the best possible design prior to
the placement of an order with some American manufacturing
concern for production and shipment for use in China. The Lab¬
oratory was able to secure the services and the designs of an
American engineer who had been engaged in the gasogen field
in France and who managed to leave France just after Hitler
arrived there. The experimental unit built for the Chinese and
tested in the Madison-Baraboo hills area was of a type designed
for the burning of charcoal. Comparable tests are now under
way with a type of British design intended for use with raw
wood, such as sawdust. Its inventor is temporarily on the staff
of the Forest Products Laboratory. The charcoal unit was suf¬
ficiently satisfactory to the Chinese officials so that a sizable con¬
tract was let under Lend-Lease for manufacture and shipment
to China. The sawdust unit will be ready for testing in the near
future.
Different fuels, such as nut shells, coke, anthracite coal, wood
or charcoal, can be used in properly designed gasogens. Of these,
charcoal is generally considered the best fuel, for it is relatively
free of resins, tars, oils, and of acid-forming substances, such as
sulfur, which would be injurious to the unit and to the engine.
The danger of tar or acetic acid formation, which is present in
using wood, is absent when good charcoal is used. A charcoal
gasogen unit will also weigh less than a wood unit. For these
reasons charcoal gasogens are in more common use in foreign
countries even though wood is a cheaper fuel.
It has previously been held that if raw wood is used, the
pieces should be of fairly uniform size, about that of a man’s fist,
and dried to a fairly uniform moisture content of 10 to 20 per
cent. The design now being prepared for test is intended to per¬
mit the use of green sawdust.
The remainder of this paper will relate only to charcoal be¬
cause it is too soon to say anything about the sawdust unit.
Sweet — Gasogens
437
Equipment and Principles Applicable
to Charcoal Gas Generators
A gasogen unit is made of three main parts: the gas pro¬
ducer, the cleaning and cooling equipment, and the mixing de¬
vice.
The gas producer is generally in the form of a vertical cyl¬
inder, and consists of a gas-tight fuel hopper to feed the fuel by
gravity into the fire zone.
The gas is formed in the producer by incomplete combustion
of the fuel. The rate of combustion is controlled by the suction
of the engine. Air is delivered at one zone in the fuel bed where
the glowing carbon combines readily with the available oxygen
in the air to form carbon dioxide with the evolution of much
heat. The fuel through which the carbon dioxide passes must be
sufficiently hot so that the glowing carbon reduces the carbon
dioxide to carbon monoxide. Some of the water vapor present
reacts with the glowing fuel to form hydrogen and carbon mon¬
oxide, and volatile tars and resins are converted by the same
means to methane and carbon monoxide. It is all these gases
which, upon the proper addition of air, become the combustible
mixture.
The gas leaving the producer passes through the cleaning and
cooling equipment before it enters the engine. When the gas
leaves the producer it carries with it particles of charcoal dust,
soot, ash, and tarry substances; all must be removed in the fil¬
ters.
The gas must be cooled to as low a temperature as possible
before entering the engine so that its maximum density is real¬
ized. In some cases, the surfaces of the filters and the inter¬
connecting pipes are sufficient to give good cooling; in others,
special coolers are provided. The mixing device provides the
proper proportions of gas and air to form a combustible mixture
before it enters the engine.
The space and weight requirements of the producer are such
that the pay load is reduced by about 10 per cent.
Operation
After the producer is filled with charcoal fuel, the fuel door
is clamped down and the fuel ignited. A draft is created through
the charcoal, either with a hand-operated blower or with the
438 Wisconsin Academy of Sciences , Arts and Letters
suction of the engine started on gasoline. When starting with
gasoline, the change-over valve is partly opened so that the
engine draws air through the fuel. This valve is gradually
opened wider, cutting down the suction through the carburetor
and increasing the suction through the gasogen until the engine
is running completely on producer gas. From a cold producer to
full power using charcoal, the following figures are quoted by
various authorities: low, 3.5 minutes; high, 14 minutes; aver¬
age, 10 minutes. This depends upon the season of the year, type
of gasogen, and quality of the charcoal.
A truck driver must be trained to operate a gasogen prop¬
erly; this can, however, be accomplished in a very short time.
He must remember that gas must be manufactured before it can
be used in the engine, and therefore, the engine should be oper¬
ated to favor the fire zone. It is necessary to keep the speed of
the engine up and not let it drag on heavy pulls. For this reason,
and also due to reduction in power, it will be necessary to shift
gears more frequently.
Although the gas produced contains carbon monoxide, which
is highly poisonous, no unusual precautions must be taken while
the gasogen unit is on the road. While the engine is running,
there is little chance of gas escaping due to the suction from the
engine. When the engine stops, a slight pressure is created, and
the gas will leak out of the air inlet and through the mixing de¬
vice. An absolutely essential precaution is that the unit should
not be placed in a closed space immediately after stopping the
engine.
In gasogen operation additional time is required for starting
and refueling. With charcoal the driver will have to stop to
refuel about three times as often as he formerly refueled with
gasoline. Besides this, five per cent of the operator's time will
be spent in cleaning filters and the generator.
Comparison of Power Developed
by Gasoline and Producer Gas
About 13 pounds of charcoal is the equivalent of one gallon
of gasoline. The gas produced by a gasogen using charcoal with
good operation will have a heating value of about 140 B.t.u. per
cubic foot. Air must be mixed with the gas before it can be
burned in the engine, and the heat value of this mixture is about
Sweet — Gas o gens
439
@8 B.t.u. per cubic foot. The heat value of combustible gasoline
vapor mixture is usually quoted as about 94 B.t.u. per cubic foot
which means that an engine operating on gasoline will develop
between 30 and 40 per cent more power than when running on
charcoal gas. The resistance of the flow of gases through the
fuel bed, piping, and filters is greater than the resistance through
the carburetor. These two factors mean that about 50 per cent
as much power can be expected when operating on charcoal gas
as when operating with gasoline. Therefore, unless the truck is
overpowered, either an increase in running time or a reduction
in the load will result.
On gasogens equipped with valves for readily changing from
gasoline to producer gas it is possible to step up the power by
operating partly on gasoline. If necessary, gasoline alone can be
used on extremely hard pulls.
To overcome the resistance to gas flow through the fuel bed,
piping, and filters, the charcoal gasogen unit built at the Forest
Products Laboratory is equipped with a supercharger driven by
a belt from the fan shaft.
General Results of Road Tests
with Gasogen-Equipped Truck
The results of the road tests by the Forest Products Lab¬
oratory on measured and charted routes in the Madison and
Baraboo hills area with a two-ton load and holding to a maxi¬
mum speed limit of 35 miles per hour are in general as follows :
Charcoal Gasoline
run run
Average miles per hour actual running time ... _ _ _ 23.8 32.7
Per cent of time not in high due to hills ............. .23.0 3.8
Number of hills necessary to drop to first ...... _ 7 None
Number of hills necessary to drop to second . 14 1
Number of hills necessary to drop to third . . 9 5
Number of hills not made in high ..... . 30 6
Later, with a unit of the same type modified in certain re¬
spects and installed on another truck and tested in a less hilly
area near Kalamazoo, Michigan, the following results were ob¬
tained, still operating on the 35-mile-per-hour speed limit for
both gasoline and charcoal gas:
Charcoal Gasoline
Average miles per hour actual running time ....... .30.5 32.1
Number of hills necessary to drop to fourth gear .... 2 None
Number of hills in high gear where speed
dropped below 25 miles per hour . . 12 1
440 Wisconsin Academy of Sciences , Arts and Letters
On long steep hills the gasogen-operated truck has to drop
one gear lower than when gasoline is used.
It must be borne in mind that the manufacture of a gasogen
takes several hundred pounds of steel and a few pounds of metal
alloys which tend to throttle its use in times of metal shortage.
No close figures are available as to the probable cost of the
equipment installed on a truck. Even if manufactured in quan¬
tity, however, the cost would probably be from $350 to $450.
Thus only with vehicles which require a large annual consump¬
tion of gasoline can the cost of the equipment be written off by
savings in fuel cost in this country. Where gasoline is not avail¬
able at the usual prices and with usual ease, the case for gaso-
gens is better.
PROFESSOR BEATTY'S INTERPRETATION
OF SHAKESPEARE
Julia Geace Wales
University of Wisconsin
There is something unique about spoken commentary — com¬
mentary called out by the reading of a great piece of literature
with a class present. It is too living a thing to get into a book ;
colloquial paraphrase, contemporary application, rhetorical
question — these escape the record. Especially was this true of
Professor Beatty's course in Shakespearean Drama (English
37). The play never subserved the lecture; the lecture was there
for the play. Those of us privileged to sit in on the course looked
forward to each hour as truly an hour with Shakespeare.
Hence it is hard to illustrate the process in brief space. In
order to give the commentary, one would have to give the play ;
they ran antiphonally.
Some parts of what I have attributed to him may have been
quotations, for I have depended on my own hastily taken notes,
which let many things slip. He was full of the poets and other
creative writers. Many a point depended on one's recognizing
a context. He kept us aware of the stream of English poetry,
bringing in sidelights from Chaucer, Spenser, Milton, Coleridge,
Wordsworth, Keats, Tennyson, Browning, Kipling, Housman,
Bridges. He used English poetry — -used it for what it is for , to
know it by heart. His knowledge was “easy as an old shoe."
He was deeply read in the older critics, but gave heed to the
new ones too, sometimes differing sharply, sometimes accepting
with enthusiasm, but always centering interest in the immedi¬
ate problem — the illumination of the play itself. He would re¬
view the current controversies and pose their questions. But he
was never caught by dogmatism. His own imagination kept its
freedom. He loved whatever gave the reader freedom and breath¬
ing space. He hated theories that measured by rule, or applied
touchstones alien to the matter in hand. Common sense and
imagination were his guides, and everyday speech — without
technicalities — his medium. Much of his teaching was in ques-
441
442 Wisconsin Academy of Sciences , Arts and Letters
tions that you had to think about. He put the factors before you,
but left you to think them out, told you to read and keep your
mind open.
Despite insistence on freedom of approach, however, he never
minimized difficulties or the need of hard work. “You ought to
have your clothes torn going through Hamlet, because you are
going through a thicket. You can't ride through in a limousine.
Observe. Learn to see straight. Know the play ; know the notes ;
know it."
The sense of place in the plays came to us augmented by the
lecturer's own sense of England; and he had it from both per¬
sonal tradition and frequent brief residence abroad. His was
the England which exists in the imagination of the scholar-
traveller who knows her history, her novels, her poetry. It is a
place out of time, not coinciding with the fact of the past nor
actual in the present, but permanently real and indestructible.
He knew the “worm-eaten holds of ragged stone" where once
lived these wailing women and terrified children and tired old
dying kings. And he knew the English countryside too, in all
seasons and weathers.
Throughout his teaching of Shakespeare Professor Beatty
stressed the poetry most of all. He insisted that Shakespeare
“was a born poet who learned to be a dramatist." He would say,
“See how he keeps the action cooling its heels while he gives us
quite unnecessarily beautiful poetry. ... He doesn't trouble to
save his poetry for his good people ; he is lavish with it."
And by the poetry of the plays he meant more than the great
lyrical passages, though he stressed these; more also than the
flashing single lines, which he always caught when many readers
would be carried past them by the momentum of the drama. It
was the poetry of the whole play that he chiefly meant, of the
world of the plays — something that he never defined, but that he
assuredly conveyed to us.
So it was that he gave us Shakespeare — rescued from
schoolroom tasks, from any tyranny of scientific history, exact
scholarship, theoretical criticism (though he made these good
servants), rescued from a changing and perilous world; —
Shakespeare, and with him a timeless England, English flowers,
English horses, English ships, and robust English laughter from
Chaucer down.
Wales — Beatty's Interpretation of Shakespeare 443
He had a keen interest in how the plays had been acted ; not
as mere matter of history, but to shed light on the living prob¬
lems of the characters and how their lines should be read. He
called up the shades of great actors he had seen. Professor Beatty
could have been an actor himself. I should have liked to see his
Richard III, his Falstaff, his Prospero.
Perhaps one reason he liked to work with Richard III, was
that this play called in so much imaginative material from its
background: history, legend with its prejudice, the literary and
theatrical tradition, and the type of the villain—' “the villain who
was a villain and stuck it out.” He made us feel the richness of
this realm — but not in terms of scientific work-a-day history and
examinations. No; it was the history of childish picture books
come alive again, when those bearded, armored kings were apt
to be either “good” or satisfyingly diabolical.
“There is something fine and hearty about Richard III.” We
were made to feel the gusto with which Richard manipulated his
puppets, knocking them about like ninepins, twirling them like
tops, playing cat and mouse, sending a bishop “trotting” off for
strawberries— “A bishop as subservient as this!” — stopping a
funeral procession with “a dramatic challenge to the super¬
natural (wounds bleed in the presence of a murderer)” ; answer¬
ing Elizabeth's horrified What thou? with an “imperturbable”
Even so; what think you of it, Madam? . . . “Milton must have
learned much about Satan from Richard III.”
It was the diabolical humor of Richard that he stressed chief¬
ly, until the last act, and there the strangely lyrical element that
makes him human. Of the contrasting camps, Richmond's and
Richard's, “Shakespeare is more interested in the tragic scene.
Stir with the lark tomorrow, gentle Norfolk. . . . Famous line,
beautiful line. Saddle White Surrey — that particular horse. . . .
The Ghost of Buckingham says to Richmond : And Richard falls
in height of all his pride. King Richard starts out of his dream.
Give me another horse: bind up my wounds. See the connection:
he dreams that his horse has been killed under him. ... In the
last scene the dream comes true. His horse is slain, and all on
foot he fights /Seeking for Richmond in the throat of death./
Rescue, fair lord, or else the day is lost. Enter King Richard:
A horse ! a horse ! my kingdom for a horse!"
He never tired of teaching the great trilogy of Henry IV-V,
444 Wisconsin Academy of Sciences , Arts and Letters
“the epic of the Lancastrian house.” He loved the spaciousness
and freedom of these plays, their very historical inconsistency,
which gave them timelessness. Less dark and far away than
Richard III, though actually about an earlier time, glamorous,
full of brilliancy, it was in their zest of life that he liked to pre¬
sent them. “Note that this period is mediaeval; but the plays
are not mediaeval; they are Elizabethan.” He went over the
“old jolly, turbulent play” — The Famous Victories — to show in
detail what the raw material was like and what Shakespeare did
with it. Bringing in the work of several modern scholars, be
traced the growth of the Falstaff group, how Shakespeare en¬
larges the surroundings of the Tavern. . . . “An unparalleled set
of comic characters — a prodigality of creation unique even in
Shakespeare . . . such variety!” He adapted Dryden: “Here is
God's plenty.”
So he made the action escape the bounds of the theatre : the
depth of night on the highway, the tethered horses ; the lantern
in the innyard and the sharp air of dawn — “Ostlers, a class of
men all by themselves” ; Glendower calling up spirits — the super¬
natural alwrays led to rich digression; Hotspur on his horse —
“Shakespeare, the country boy; he had as much Greek as the
average Ph.D. ; but horses, he knew about horses” ; the wakeful
king in the palace, thinking of the happier lowly folk of his
kingdom, the sailor on the giddy mast — how often the lecturer
stopped over the sea passages, bidding us hear them with the
ears of a maritime people ; the lighted tavern full of noise, Pistol
at the door — Shall we let him in? “Too bad Pistol wasn't in
Part I” ; 1 see no reason why thou shouldst he so superfluous to
demand the time of day . . . . Play out the play. I have much to
say in the behalf of that Falstaff.
“If you don't appreciate Falstaff, you are too young. . . . No
use trying to make Falstaff respectable ; no use trying to forget
any of him. . . . Whatever contrasting things you say of him,
he is both and neither; he remains unclassified. You can't cap¬
ture him. He exists in the free world of Shakespeare’s imagina¬
tion — airy nothing — two hundred and seventy-five pounds. Here
is prodigality of creation. ... He really died in Henry V — a
scene unparalleled in all literature — just exactly as he ought to
have died. ... You should never rationalize him more than
Shakespeare has rationalized him. . . . Falstaff is elemental ; he's
Wales — Beatty's Interpretation of Shakespeare 445
cosmic. His lies are cosmic lies — a world we have no conception
of. The Lord surveyed his work and found it good. It does not
say, found it comprehensible. To create does not mean to under¬
stand. Creation does not work from a system or formula. Get
some savor of the welter of life that is in Shakespeare ; the wel¬
ter of life itself. Chaucer knew this world. It is the only world
we have. This is not to say this world is an anarchy. For with
creation goes a certain order ; but not until you have it all. Hence
you can't make a formula. Our world was made out of chaos;
there is some chaos still. . . .
“You must allow humor to be in any situation in life. There
is a time to laugh, and that is always, especially when you are
most solemn. This is English. The critic will have Shakespeare
saying some ultimate thing that excludes the humor. Beware of
those who are consciously summing up the wisdom of life.
Shakespeare's characters are hard to come at if you lack humor.
. . . Don't oversimplify. Note the departure from drama to
poetic commentary."
He reviewed Sidney's Apology for Poetry. “Sidney has no
conception whatever of romantic comedy; he bases his ideas on
what has been done ... Do you want your dramas to get down
to business? Or do you want all this unnecessary poetry? . . .
Don't leave it at a phrase, or a partial judgment. High comedy
is difficult. These are not stories just going to an end. They have
length, breadth, thickness. Each person matters for himself.
A gay mood — -a complex whole : plastic, plastic. . . .
“Ben Jonson wrote reasonable plays, banished this nonsense.
Ben Jonson would have the best of the argument. This of
Shakespeare’s is not a reasonable world ; it is a world of make-
believe. These ingredients were expected, but he liked them too.
The dressing up is part of Shakespeare's look at the world. He
knew the fairies at first hand ; they were part and parcel of his
mentality. Don't try to explain him on Ben-Jonsonian grounds.
Ben Jonson abandoned the native tradition and took a new
rationalistic road. Shakespeare took the old road, used the old
stuff. . . .
“Beware of the people who believe that literature must have
a mission. . . . What a ridiculous world this is! You realistic
young folk are apt to be hard on these people. They are innocent
and naive. . . . I'll give you Malvolio — but he is not the play. . . .
446 Wisconsin Academy of Sciences , Arts and Letters
The action is thin, I grant you. These comedies are difficult of
appreciation because they are impalpable. Consider them in
terms of the Forest of Arden ; don't try to make them live in our
world. ... Wait till you're grown up, until your sense of humor
develops."
He often began the course with the uproarious Comedy of
Errors : the riot at the first performance (recalling a campus
parallel), when “the Temple people didn't think they had good
enough seats, and left in disorder" ; the Elizabethan world show¬
ing through the foreign disguise: Enter the Hangman — “with
his axe on his shoulder; people were given to going to execu¬
tions." Book in hand, he demanded the kind of attentive reading
that gets each irony, each repeated motif, each refrain and
theme song. “Now the fun begins. Which Dromio is it? The
effect of this play is cumulative; gets funnier. . . . It's a joke
either way, if you're right in your guess, or wrong." He would
point up little comicalities with his zestful chuckle. “Antipholus
of Syracuse is always about to leave town — but never does. . . .
Why is it that the world finds such nonsense so wise? Why is
there such a thing as comedy?" And then the lyrical element,
so strangely interwoven — he gave time to that.
He would touch off a character in a phrase. On the Duke and
Valentine in The Two Gentlemen of Verona : “The wily grey¬
beard listening to the wisdom of youth. . . . The scene acts as
immensely humorous — the young whipper-snapper instructing
the elderly man of the world. . . . Valentine is good at writing
testimonials. . . . Cardboard outlaws. . . . Valentine has passed
the proficiency test in language. . . . The ever-ready Eglamour
entirely and disinterestedly devoted to helping ladies in dis¬
tress. . . . Note the poetry breaking in : The uncertain glory of
an April day.”
He made himself a link with the past, when it came to the
sources of A Midsummer Night's Dream , and was full of fireside
tales from books and life — the stuff of the fancy that went to the
making of the play. Afterwards if you wanted to look up learned
footnotes on these things, you found that their content had been
delightfully served up ; the cupboard was bare. But it was only
the imaginatively edible that he gave us. “Don't worry about
anything that Shakespeare didn't worry about. Never mind how
big the fairies were. A fairy is just as big as a fairy. . . .
Wales — Beatty's Interpretation of Shakespeare 447
“I don’t know at what point Shakespeare began to get the
idea of the play A Midsummer Night's Dream. Maybe the play
began when he was a boy visiting his grandmother. ... If the
fairies were going to be seen by anybody, it would be the me¬
chanicals. The reason we don’t realize this at once is that with
us the fairies are derived from books and not from life. Most of
the people who saw the play had seen some fairies. Shed your
disbelief. The fairies are as real as the Ghost. Oberon and
Titania are bookish fairies; Puck steps in from life. English
fairies have attached themselves to the train of Oberon. . . . The
wedding is three days off. Now how put in the time? . . . Shakes¬
peare knew Chaucer quite well. A lucky thing he did. I wish
he’d known him better. The Knight's Tale is one of the greatest
narrative poems in English literature. . . . Bottom is a mon¬
actor [he may have invented the term] .... The quality of folk
belief is that it is prosaic and poetic — at one and the same
time. . . . There is many a house still in Ireland- — and in England
too — where the fairies lived; so you have to do a more purely
aesthetic thing than Shakespeare’s audiences did. Shakespeare
himself knew the fairies. I’m sure he was nervous on some
kind of nights. He’s here reviving the memories of his child¬
hood. Also he read. This is partly book knowledge; but not
primarily. He did not read up for this play. Vivid pictures
of low life here — equal to Hogarth. . . . What keeps the fairies
alive? They are alive. Do you believe in the Universe? I never
should have thought of it. You’d better entertain it. . . . There
were ways to find out if a baby was a changeling. That’s why
they hastened to church and got it christened — so that it couldn’t
be taken. ... A wedding is a time you’d better have the fairies
on your side.” And much more lore of the same kind. Wild
geese that the creeping fowler eye/ Or russet-pated choughs ,
many in sort,/ Rising and catving at the gun's report — Observa¬
tion of a country-bred man. . . . An important part of the play
at the end-— too often neglected. Very important to placate the
fairies so that they bless the wedding ; should be given time with
dances. ... If you get too dramatic you are going to miss three
quarters of Shakespeare. . . . May dew gathered by the fairies.
. . . Bathe the face with it ; it gives beauty. . . . Leave flowers on
the window sill for the fairies to touch. . . . The greatest criti¬
cism of A Midsummer Night's Dream is Puck’s at the end : If we
448 Wisconsin Academy of Sciences , Arts and Letters
shadows have offended ,/ Think but this , and all is mended,/
That you have but slumber'd here,/ While these visions did
appear./ And this weak and idle theme,/ No more yielding but
a dream,/ Gentles, do not reprehend. Shakespeare disappears if
you try to analyze it. Yet it needs annotation. Of imagination
all compact. Needlessly beautiful.” He said of the little western
flower passage, dismissing controversy, “This is good enough to
mean just itself. Hold it as poetry — don’t pass it on until you
must. . . . What is the meaning of the play ? Does it mean any¬
thing? Is it a symbol? a metaphor? The less said about that the
better. It is difficult to prove that Shakespeare ever wrote a play
symbolical of anything. Poets pay the penalty for being poets
in this way ; they have a habit of taking a simple fact and using
such vivid and intense language about it that people think it
must have meant something else — can’t believe that the simple
situation in itself could have had all that content. ... I know
a bank where the wild thyme bloivs. Just a memory of Stratford
— nothing more.”
Of Much Ado About Nothing Professor Beatty said : “A curi¬
ous play: stuff not plausible; stuff highly plausible. The clever
people are fooled ; the fools solve the problem. . . . Shakespeare’s
men and women are in a vacuum as far as any realistic back¬
ground is concerned.” He was excellent on Dogberry and the
Watch. Let us go sit upon the church bench till two and then all
to bed — “A very sleepy scene.” The friar’s plan: “An elabora¬
tion of the plot that never was needed. It is not really this that
works the solution. . . . Shakespeare works by scenes, by acts.
The reason he does is that he works by creation. Dogberry and
Verges were pulling Shakespeare’s coattails asking to be taken
into something.”
He said of Twelfth Night: “Observe the subtlety and cer¬
tainty of the phrasing and the quality of the poetry. Here the
lyric secret is recaptured as in Romeo and Juliet, and transferred
into the realm of comedy — a world in which poetry is the nat¬
ural thing. . . . Sir Andrew is the most consummate idiot in all
Shakespeare. ... A fine jolly play; a lot of nonsense; also seri¬
ousness — human rather than social. Contrast Ben Jonson and
his social criticism, satire, and social conscience; a corrector of
society, bound to be more realistic, he pictures the age more
clearly than Shakespeare. . . . [But] do not make the mistake
Wales— Beatty's Interpretation of Shakespeare 449
of thinking that Shakespeare represents the literature of escape.
He takes life out into the Forest of Arden. Not only can he create
people in the world but he can first create the world. Don't
patronize Shakespeare because of your admiration of Ben Jon-
son, or vice versa. . . . Feste is not young; he dates back to
Olivia's father. . . . The cathedrals were schools of voice train¬
ing. Feste sings Come Away Death. This is the quality of the
clown. There is a tragic note in his songs and sayings. ... We
must not simplify Shakespeare and misinterpret the clown.
Feste's deeper note is sounded whenever he appears. . . . Why
does Shakespeare have so many shipwrecks? Why, because of
London; the ships of the world were in its harbors. Shakespeare
knew ships well, though never at sea ; he lived in a cosmopolitan
world. . . . Sebastian is a gorgeous character; healthy; no pho¬
bias ; zest of life ; brother of delightful Viola. He acts like six-
foot-two-inches." And at the end of the Clown's song about
The rain it raineth every day , he made final comment : “Surface
jollity but a constant dipping down into something deeper."
In discussing The Winter's Tale Professor Beatty gave most
of the time to the fourth act. “The sweet of the year — Some of
this garden stuff must have gone over the heads of the theatre;
it would be understood at Stratford." In looking for the sources
of beauty in the plays, he was always very loyal to Shakespeare's
home town. “The idea that art itself is nature doesn't convince
Perdita. You must know the garden lore to get the beauty and
pathos of the scene." And he would expound it.
The Tempest opened vistas into the kind of background he
gloried in — the sea, the voyages. And in this play, more than
anywhere else, he was tempted to read in symbolism; but he
resisted valiantly.
“Written by a man that knows about ships for an audience
that knew also about storms. The seaman orders the aristocrats
about, supreme on the ship, contemptuous of the landlubbers —
the prime minister, important at home. . . . All a kindly parody
of witchcraft; all harmless. Shakespeare takes the dark witch¬
craft and opposes a contrasting magic, a benevolent. Beware of
reading in too much symbolism. . . . The play is carried on in a
more open atmosphere than any romance; salty; as in Hakluyt
and such books. . . . Gonzalo is a kind of glorified Polonius ; the
wise man. Shakespeare has read the wise books. . . . Dark back -
450 Wisconsin Academy of Sciences , Arts and Letters
ward and abysm of time — not historical time, but the time of
consciousness. . . . Why shouldn't the poet know more about the
human mind than professors of psychology ? . . . My library . . .
volumes that I prize above my dukedom. Shakespeare often
speaks of the quiet life. . . . Fairies were good as long as you
mastered them. . . . Mankind is beset on every hand by malevo¬
lent powers. You have to master them or they master you. A
realistic world ; not one of pleasant fancy. ... [Of the drunken
scene] This is the way civilization reached Caliban; but — that
way madness lies ; that is turning the play into a moral lesson ;
terrible irony here. . . . When Shakespeare creates, the character
steps out of the frame of the story. Compare what Goethe said,
that Hamlet has a life outside the play. Shakespeare must have
seen the Prince of Denmark before he found a place to put him.
You see Miranda in several dimensions. ... We are such stuff as
dreams are made on. Like the stage curtain. . . . Bear with my
tveakness; my old brain is troubled. You are young; I do not ask
you to enter into my thoughts. ... It is not unusual to find artists
returning to the primary things. Shakespeare never got far
from them. In all this you have wonderful poetry. What is it
that Prospero knows? Magic? Yes ; he puts that by. What is the
central story? The whole play is just to bring Ferdinand to the
Island, where Miranda is. . . . This story is surrounded by all
sorts of strange things. ... It has the quality of setting the
critics to work as if it were an allegory. . . . The girl falls in
love. This is more wonderful than the esoteric. Why make this
fetch and carry for other departments of life? . . . Spenser's
mind had to work with general notions; Shakespeare thinks in
the concrete. Did he in the end become more dependent on gen¬
eral ideas? I don't believe it. . . . A boy lying in the grass —
means a boy lying in the grass. The prosaic person is not satis¬
fied with the single figure — has to mean youth. But the artist
meant the boy. Goethe means Faust. The prosaic person will
not believe that the poet attaches the ultimate value to the thing
itself — not to the abstraction." However, he did go as far as
this: "Just entertain in your mind penumbral shadows. For
Shakespeare is here contemplative. ... Yet these do lend them¬
selves to symbolism ; but resist the temptation to reduce them to
set terms. . . . Prospero in the background knows what is going
on better than the young people do. . . . Comedy comes from
Wales — Beatty's Interpretation of Shakespeare 451
depths as deep as tragedy comes from.” He quoted a colleague,
Professor W. E. Leonard : “If you go to the deeps where there
is light, you are doing as great a thing as going to the deeps
where there is darkness.”
Professor Beatty repeatedly insisted on the importance of
going back to the poets who have interpreted Shakespeare : . . .
“Consider Coleridge, Goethe, etc. who treat creation as creation.
. . . Hamlet is not about what the prose people think it's about.
When Goethe is talking about Hamlet , he is not talking about the
same thing as the prose people are. ... It is often from foolish¬
ness — from the vagrant stuff — that poetry is made. . . . Most
students will rise to poetry if you catch 'em young. . . .
“Shakespeare's plays are practically all made out of books —
out of his reading. ... He read in a random way — supplemen¬
tary to his business of making a living ; read here and there, this
and that and t'other; and out came the poetry. . . . The books
start it, but Imogen comes out of nowhere. Plant seed and the
marvel is what comes out. He has both worlds of comedy and
tragedy. My advice: read both Shakespearean comedy and
Shakespearean tragedy when you are not inhibited by practical
considerations, when you can follow up an idea to its logical con¬
clusions. Read Shakespeare, and the world will take care of it¬
self. What is the matter with the world is that it has forgotten
its Shakespeare. If people would behave as if it were a Shakes¬
pearean world — and die so too — what a world it would be ! I hope
that in twenty-five years you'll believe that. . . . Don't forget the
Forest of Arden, where there are no clocks .”
In dealing with the tragedies, too, he mediated between
scholarship and the ordinary reader, taking up learning into
the activity of the imagination. The old barbaric story of the
Danish prince, the wanderings of Othello, pre-historic legend,
fairy tale of the family of Cinderella, witchcraft, astrology, ap¬
paritions, the dark lore of madness, every kind of homely folk
lore — he let us see these in successive transmutations that we
might feel what the poet's alchemy finally made of them — not
poetry alone, not tragedy alone, but the essence of tragic poetry.
The story of the star-crossed lovers seemed strangely real in
“the two hours' traffic'' of Professor Beatty's lecture room. “The
story has a long, long history- — architypal. . . . Three young men
who troop together— Romeo, Benvolio, Mercutio. Street scenes.
452 Wisconsin Academy of Sciences , Arts and Letters
. . . Costume party. They come as pilgrims. . . . When Shakes¬
peare’s characters come alive, they do come alive. Why did
Mercutio come alive? I don’t know. . . . This is a young man’s
play. . . . More light . . . turn the tables up. My party: have a
good time. Romeo comes out from behind a pillar. You hear his
voice. He speaks to a serving man, who is busy. . . . The lyric
refrain — the torches. You hear the poetry. . . . Tyb the cat is
on the watch. Romeo reappears in your attention. . . . Now the
sonnets — the pilgrim motif. . . . Ellen Terry acted Juliet’s nurse
so well that it wasn’t acting; she was the nurse. What's he that
follows there that would not dance ? Ellen Terry goes to find out.
This is a very important moment. It must get time-value and
clear, telling emphasis. Terrible effect of Romeo and a Mon¬
tague. . . . They say Shakespeare has double time — two clocks.
At the observatory they have star time.” And so on through the
scenes until the tragedy came home in pity and beauty. '‘Shakes¬
peare invented little, but he invented all.”
“ Hamlet is no play for Hamlet to be in. . . . There is some¬
thing wrong with Hamlet; call it perturbation. Shakespeare
knows about men whose minds are perturbed. . . . Seems, Mad¬
am! a match to powder; an explosion. . . . The King is a very
capable man, a murderer, and a gentleman. . . . An attempt has
been made to make the Ghost subjective so that Hamlet speaks
the Ghost speech. This is nonsense !” He liked J. Dover Wilson’s
note on russet in Horatio’s speech about the dawn. “I would
add the shepherds,” he said, having a fancy for linking it with
the imagery of the preceding speech and the shepherds on the
hills under the benignant stars in the season when the bird of
dawning singeth all night long. . . . “Wonderful dialogue.
Shakespeare gives not only the image but the lyrical image —
loaded up with poetry.” On Polonius, admit no messengers , re¬
ceive no tokens: “Ophelia obeys — against all her own feelings;
hence her insanity later. Simple — perfectly simple and clear —
simple as insanity. All the ultimate horrors are in this play.”
Of the play scene : “Hamlet is still punishing Ophelia for being
in the plot. . . . Probably Shakespeare did much re-arranging in
Hamlet ; maybe he experimented ; maybe second thoughts aren’t
always the best. . . . There is some criticism written with a view
to squaring Hamlet with Aristotle. Can’t be done. Aristotle did
not know Hamlet. If he had, he (Aristotle) would have been a
Wales — Beatty's Interpretation of Shakespeare 453
better and wiser man. There is such an animal ; Hamlet exists.
. . . Aristotle says the character is second to the plot. As far as
Hamlet is concerned, don't you believe it. Hamlet the person is
central. There is a proverb : Hamlet with Hamlet left out equals
nothing. Hamlet is his own lago ; Hamlet is his own Lady Mac¬
beth. Follow Hamlet himself. Don't invent things that aren’t
there. As to what Shakespeare doesn’t say, never mind. . . .
You are a guilty creature sitting at a play. That's what you
have to be to get this — not a rationalistic professor talking about
it." On Hamlet he went back and drew deeply on the criticism of
Goethe and Coleridge, feeling, as he often said, that as poets
they perceive the problem more profoundly than most critics.
But he said of each, “His solution is less important than his pre¬
sentation of the difficulty. . . . The problem is in the contradiction
between the circumstances of Hamlet and the character. Shakes¬
peare had many more characters looking for plays than he had
plays .... The irreconcilable things are the play. The world is
not out of joint except as Hamlet comes into it. . . . The problem
is one of keeping within the play. Can we assume that literature
and life are one ? Or are they only parallel ? Do they ever touch,
necessarily? . . . This is the most popular play in any language.
Why? What are the bases of the aesthetic experience? Beware
of Polonius who has a complete theory of the whole. . . .
“The Turk nearly overwhelmed Europe. Shakespeare must
have had this in his imagination-— Othello the great general
against the Turks. A magnificently capable mind; a long an¬
cestry behind him." On III :ii : — “Othello the normal, capable,
busy man. . . . Desdemona: I saw Othello's visage in his mind .
And he was neither black nor white; he was Othello. . . . But
still the house affairs would draw her thence ,/ Which ever as she
could with haste dispatch,/ She'd come again and with a greedy
ear/ Devour up my discourse . An English domestic scene ; mid¬
dle class; the lady of the house busy with her housekeeping.
More like Stratford than Italy. . . . Amazing how precise a no¬
tion we have of Desdemona and how little she says. . . . Othello
is charged with using magic- — a serious charge in those days. . . .
She loved me for the dangers I had passed ,/ And I loved her that
she did pity them. Profound psychology. . . . Thy escape would
teach me tyranny. Shakespeare is not sentimental ; parents can
be hard as granite. . . . Othello is one of the great masters of
454 Wisconsin Academy of Sciences , Arts and Letters
language in Shakespeare (perhaps Falstaff is the greatest). . . .
If Iago had not had so many fools to work on, he could not have
succeeded. ... In real life it is amazing what some people will
do for a slight thing. What makes Iago convincing? Iago. The
explosive charge is in Iago, not in the external occasion”. . . .
III:iii: — “Perhaps the greatest scene in all Shakespeare. The
power here lies in concentration. . . . Good name in man and
woman , dear by lord,/ Is the immediate jewel of their souls.
No other dramatist would put such a speech in the mouth of such
a man. ... If thou dost slander her and torture mei/ Never pray
more. Note the organic movement away from the iambic. . . .
Like to the Pontic Sea. In the whole passage note the verse
movement. . . . Irony piled on irony. The great evidence of her
love is used as evidence against her.” ... Of IV :ii : — “Emilia
keeps her level and Desdemona keeps hers. . . . The Greek rule
that deaths must be off the stage is a good rule. . . . Nowhere is
Othello so great as in his last speech. Shakespeare envisages his
tragedy as a surprising thing, inexplicable. Shakespeare gives
it the atmosphere of the prodigious. . . . Remember it is poetry ;
don't try to make it realistic. . . . Shakespeare gave this story
wings.” He quoted W. MacNeile Dixon on tragedy: “It presents
the worst, and excites in us the best. ... Its conclusions are not
contained within its premises. ... A kingdom inaccessible to
fortune.”
Of the plays Professor Beatty dealt with, I find my notes
on Macbeth the least adequate and my sense of his teaching of
the play the most vivid and strong. He was like Prospero with
his book; old tomes of magic, here he was, with them on his
desk, holding them up for us to see: King James' Daemonologie,
Reginald Scot's Discovery of Witchcraft , the Malleus Malefi-
carum.
He refused to let us test the action of the play by mundane
reality. It must carry its own world order with it : the palpable
power of evil; the man like ourselves caught in its mesh, dic¬
tated to against his will. He left Macbeth, it seemed to me, hard
to understand before he acts, but terrifyingly comprehensible
after he acts.
“Personally, I would rather sacrifice a motive than the
witches. If you refine the psychology, you will refine the witches
away. ... If you can look into the seeds of timd/ And say which
Wales — Beatty's Interpretation of Shakespeare 455
grain will grow and which will not/— A witch literally did that.
. . . They had power— whether you believed in them or not —
power over the innocent. All this is perfectly sound witchcraft.
They are agents of the devil. . . . They appealed to curiosity
about the future. . . . You can't understand the play unless you
believe in witches. . . . Macbeth is really a poet embroiled with
the powers of darkness. . . . The earth hath hubbies , as the water
has,/ And these are of them. Whither are they vanished?/ Into
the air , and ivhat seemed corporal melted/ As breath into the
wind. . . . Were such things here as we do speak about,/ Or have
we eaten of the insane root / That takes the reason prisoner?
This scene must have slow tempo. . . . Nothing in his life/ Be¬
came him like the leaving it; he died/ As one that hath been
studied in his death/ To throw away the dearest thing he ow'd/
As 'twere a careless trifle. Even so Shakespeare throws away
these bits of poetry. . . . The task of the witches is to destroy the
innocent. They dwell in waste places. Sometimes they have
strange limitations of power. . . . The thing has the impelling
force of a duty. If it were done when 'tis done/ Then ' twere well
it were done quickly. If dead men would ever stay dead. Con¬
trast What's done is done . What's done cannot be undone.
. . . At the south entry. It was Hell's gate that the knocking was
at. . . . Banquo's Ghost is a material ghost. The murdered man
kept his word. . . . Name a ghost and he will appear. You must
'suspend your disbelief' 'willingly'. There was no such difficulty
in the Globe theatre. . . . How goes the night , boy? The moon is
down. Night . . . night. . . . Methought I heard a voice cry ' Sleep
no more',/ Macbeth doth murder sleep. . . . Sleep . . . sleep. . . .
After life's fitful fever he sleeps well."
He read all the greatest passages, with their lyrical repeti¬
tions, letting them produce their own cumulative effect, the
longing for the wholesome, the holy terror of the evil thing.
"Shakespeare is the only one who made a tragedy of the
Lear story. ... He did not follow any one version. There are
fundamental changes from all the versions we know. . . . Spen¬
ser and the rest became part of a consciousness that could pro¬
duce tragedy. ... You know from the beginning that he is going
to make it tragic. . . . Cordelia says one hundred lines, but see
how we get to know her from what others say of her. . . . The
cocksureness of Cordelia, her certainty that she is doing right —
456 Wisconsin Academy of Sciences , Arts and Letters
that is unattractive. . . . France’s speech, one of the finest in the
play. How could Shakespeare be so wasteful as to let France,
this wonderful character, disappear? . . . How important is he
going to make Edmund? A vigorous man; might easily usurp
the interest; appeals from convention to nature. At war with
the powers that brand him as base. Edmund is in the sub-plot;
note how his power goes into the main plot. . . . Even in Shakes¬
peare’s day an eclipse was a terrible thing; people were afraid.
. . . The play stops to let the fool talk. And what a fool it is!
The fool almost always talks poetry even when he talks least
sense. . . . Observe how the mad imagery of Edgar is trans¬
formed into the mad imagery of Lear. . . . Fathom and a half.
Seafaring folk understand ; taking soundings on the rocks ; shal¬
low sea; danger. . . . See how this profoundly moving scene
touches the common. . . . Didst thou give all to thy two daugh¬
ters / And art thou come to this ? Nothing like this anywhere
else, even in Shakespeare. Couldst thou save nothing ? Didst
thou give them all? This scene is stark humanity — and most of
them crazy! . . . Hark! do you hear the sea? Compare Xeno¬
phon: The Sea! The Sea! . . . Gentleman: . . . Sit/ Your most
dear daughter/ Lear : No rescue? What! a prisoner? 1 am even/
The natural fool of fortune . Use me well;/ You shall have ran -
some . Let me have surgeons;/ I am cut to the brains. What
'daughter’ means to him ! . . . IV :vii : — Not incongruous now.
Sheer beauty. ... V :iii : — Dreadful things on the heel of each
other all through this play. . . . Re-enter Lear with Cordelia in
his arms. One of the most deeply affecting entrances in all
Shakespeare. Unexpected ... Is this the promised endl No an¬
swer. Nothing to be said. . . . Shakespeare makes wonderful
use of the fact that Cordelia dies first. . . . My final feeling is
that it is not solved. To my mind the insoluble incongruity is the
play . ... You ought to practice holding these plays in solution.
. . . Shakespeare’s tragedy is not reward and punishment. 'Who
can control his fate?’ . . . We are still mentally buying things
that we can’t afford. Literature is for the bitter hour [alluding
to Housman whom he had just quoted] . . . Tragedy — the es¬
sence of it — is in the thing you can’t explain. There couldn’t be
any if life could be conducted according to recipe — treatises on
morals . . . based on the idea that you can beat the game if you
know enough. . . . Some people think nothing is moral that does
Wales— Beatty’s Interpretation of Shakespeare 457
not give them fur coats and steam-heated apartments. ... In
tragedy the game is played on a familiar board according to
rules that nobody knows. ... In Shakespeare good and evil have
nothing to do with any other end. Why did these men follow
Lear? What about devotion in this play? Why such devotion?
No answer. It is acceptance that Shakespeare calls for — not ex¬
planation or understanding.”
He said the following in a lecture on King Lear which he
gave after his retirement, substituting for a colleague: “Don’t
forget the scenes at Dover — and the sea. ... We are not the
first j Who , with best meaning , have incurred the worst. Remem¬
ber that this is in the play. The wonderful thing about when
you’re down : Nothing can happen to you ; you know the worst.
The wonderful thing about the English: because they have a
sense of humor, they know the worst can happen.” I recorded
the date: April 10, 1940. This was, I think, the last time he
lectured on Shakespeare.
RACIAL CLASSIFICATIONS OF THE SEVENTEENTH
AND EIGHTEENTH CENTURIES
J. S. Slotkin
University of Wisconsin
The explorations of the 15th, 16th, and 17th centuries
brought Europeans in contact with many new peoples, and fi¬
nally scholars became interested in the problem of finding order
in the bewildering variety of peoples with whom they were con¬
fronted. This led to attempts at more or less exhaustive classi¬
fications of the races of mankind.
It will be seen from the material given that the early classi¬
fications did not differ essentially from those of the present day,
either in regard to methodology or criteria. The greatest im¬
provement has been in the refinement of the criteria used as the
basis for classification, both qualitative and quantitative.
Bernier
The first classification of the races of man known to the
writer was made by Francois Bernier (1620-1688), a French
traveller.
“Although in the exterior form of their body, and
especially in their faces, men are almost all different one
from the other, according to the different districts of the
earth which they inhabit, . . . still I have remarked that
there are four or five species or races of men in particular
whose difference is so remarkable that it may be properly
made use of as the foundation for a new division of the
earth.
“I comprehend under the first species ... all Europe,
except a part of Muscovy. To this may be added a small
part of [North] Africa . . . and also a good part of [West¬
ern and Southern] Asia. ... For although the Egyptians,
for instance, and the [East] Indians are very black, or
rather copper-coloured, that colour is only an accident in
them, and comes because they are constantly exposed to
the sun ; and for those individuals who take care of them¬
selves, and who are not obliged to expose themselves so
often as the lower class, are not darker than many Span¬
iards, It is true that most Indians have something very
459
460 Wisconsin Academy of Sciences , Arts and Letters
different from us in the shape of their face, and in their
colour which often comes very near to yellow; but that
does not seem enough to make them a species apart, or
else it would be necessary to make one of the Spaniards,
another of the Germans, and so on with several other
nations of Europe.
“Under the second species I put the whole of Africa,
except the coasts I have spoken of. What induces me to
make a different species of the Africans, are, 1. Their
thick lips and squab noses, there being very few among
them who have aquiline noses or lips of moderate thick¬
ness. 2. The blackness which is peculiar to them, and
which is not caused by the sun, as many think; for if a
black African pair be transported to a cold country, their
children are just as black, and so are all their descend¬
ants until they come to marry with white women. The
cause must be sought for in the peculiar texture of their
bodies, or in the seed, or in the blood — which last are,
however, of the same colour as everywhere else. 3. Their
skin, which is oily, smooth, and polished, excepting the
places which are burnt with the sun. 4. The three or
four hairs of beard. 5. Their hair, which is not properly
hair, but rather a species of wool, which comes near to
hairs of some of our dogs ; and, finally, their teeth whiter
than the finest ivory, their tongue and all the interior of
their mouth and their lips as red as coral.
“The third species comprehends [the rest of Asia] ....
The people of all those countries are truly white ; but they
have broad shoulders, a flat face, a small squab nose, little
pig’s-eyes long and deep set, and three hairs of beard.
“The Lapps make the fourth species. They are little
stunted creatures with thick legs, large shoulders; short
neck, and a face elongated immensely ; very ugly and par¬
taking much of the bear. . . .
“As to the Americans, they are in truth most of them
olive-coloured, and have their faces modelled in a different
way from ours. Still I do not find the difference suf¬
ficiently great to make of them a peculiar species different
from ours. Besides, as in our Europe, the stature, turn of
the face, the colour and the hair are generally very differ¬
ent, as we have said, so it is the same in other parts of
the world ; as for example, the blacks of the Cape of Good
Hope seem to be of a different species to those from the
rest of Africa. They are small, thin, dry, ugly, quick in
running” (1).
Then, as might be expected from a Frenchman, he proceeds
to consider the relative beauty of the women of each of these
races (2).
Slotkin — Racial Classifications
461
Bradley
The pre-Linnaean systematist, Richard Bradley (1666-1732),
also had a classification of human races.
“I proceed to take notice of the several Kinds of Men,
whose Difference is remarkable.
“We find five Sorts of Men; the White Men, which are
Europeans , that have Beards ; and a sort of White Men in
America (as I am told) that only differ from us in having
no Beards. The third sort are the Malatoes , which have
their Skins almost of a Copper Colour, small Eyes, and
strait black Hair. The fourth Kind are the Blacks, which
have strait black Hair: And the fifth are the Blacks of
Guiney, whose Hair is curl'd , like the Wool of a Sheep ,
which difference is enough to shew us their Distinction;
for, as to their Knowledge, I suppose there would not be
any great Difference, if it was possible they could be all
born of the same Parents, and have the same Education,
they would vary no more in Understanding than Children
of the same house” (3).
Linnaeus
Carl von Linne (1707-1778) included the races of man in his
taxonomic system. In the first edition (Leyden, 1735) of the
Sy sterna Naturae he divided Homo into four varieties :
(tEuropaeus albesc.
Americanus rub esc.
Asiaticus fuscus.
Africanus nigr.”
The last revision, that of the tenth edition (Stockholm, 1758-
59) was more elaborate.
Homo know thyself
Sapiens 1. H. Diurnus; varying by culture
and place.
Ferus on all fours, mute, hairy.
Americanus reddish, choleric, erect.
Hair black, straight, thick; Nos¬
trils wide; face harsh, Beard
scanty.
Obstinate , merry, free.
Paints himself with fine red lines,
lines
Regulated by customs.
Europaeus (4) white, sanguine, muscular.
Hair flowing, long. Eyes blue.
Gentle , acute, inventive.
Covered with close vestments.
462
Wisconsin Academy of Sciences , Arts and Letters
A for
Asiaticus
Governed by laws,
sallow, melancholy, stiff.
Hair black. Eyes dark.
Severe , haughty, avaricious.
Covered with loose garments.
Ruled by opinions,
black, phlegmatic, relaxed.
Hair black, frizzled. Skin silky,
Nose flat. Lips tumid.
Women without shame. Mammae
lactate profusely.
Crafty , indolent, negligent.
Anoints himself with grease.
Governed by caprice.
Monstrosus. . .
Troglodytes
2. H. nocturnus
Homo sylvestris Orang Outang”
(5).
Blumenbach
Johann Friedrich Blumenbach (1752-1840) undertook an ex¬
amination of the races of man. In the first edition (1770) of
De generis humani varietata nativa he classified man into four
races.
. . although there seems to be so great a difference
between widely separate nations, that you might easily
take the inhabitants of the Cape of Good Hope, the Green¬
landers, and the Circassians for so many different species
of man, yet when the matter is thoroughly considered, you
see that all do so run into one another, and that one vari¬
ety of mankind does so sensibly pass into the other, that
you cannot mark out the limits between them (6). . . .
The first and most important to us (which is also the
primitive one) is that of Europe, Asia this side of the
Ganges, and all the country situated to the north of the
Amur, together with that part of North America, which
is nearest both in position and character of the inhabit¬
ants. Though the men of these countries seem to differ
very much amongst each other in form and colour, still
when they are looked at as a whole they seem to agree in
many things with ourselves. The second includes that
part of Asia beyond the Ganges, and below the river
Amur, which looks towards the south, together with the
islands, and the greater part of those countries which are
called Australia. Men of dark colour, snub noses, with
winking eyelids drawn outwards at the corners, scanty,
and stiff hair. Africa makes up the third. There remains
Slotkin — Racial Classifications
463
finally, for the fourth, the rest of America, except so much
of the North as was included in the first variety’5 (7).
In the second edition ( 1781) he revised his classification by
dividing man into five races, to which he adhered in all subse¬
quent works.
“Formerly in the first edition of this work I divided
all mankind into four varieties; but after I had more
accurately investigated the different nations of Eastern
Asia and America, and, so to speak, looked at them more
closely, I was compelled to give up that division, and to
place in its stead the following five varieties, as more
consonant to nature.
“The first of these and the largest [the Caucasian
(8)], which is also the primeval one, embraces the whole
of Europe, including the Lapps, whom I cannot in any
way separate from the rest of the Europeans, when their
appearance and their language bear such a testimony to
their Finnish origin ; and that western part of Asia . . . ;
also northern Africa, and lastly, in America, the Green¬
landers and the Esquimaux; for I see in these people a
wonderful difference from other inhabitants of America;
and, unless I am altogether deceived, I think they must
be derived from these Finns. All these nations regarded
as a whole are white in colour, and, if compared with the
rest, beautiful in form.
“The second variety [the Mongolian, (9)] comprises
the rest of Asia. . . . The inhabitants of this country are
distinguished by being of brownish colour, more or less
verging to the olive, straight face, narrow eyelids, and
scanty hair. . . .
“The third variety [the Ethiopian, (10)] comprises
what remains of Africa, besides that northern part which
I have already mentioned. Black men, muscular, with
prominent upper jaws, swelling lips, turned up nose, very
black curly hair.
“The fourth [the American, (11)] comprises the rest
of America, whose inhabitants are distinguished by their
copper colour, their thin habit of body, and scanty hair.
“Finally, the new southern world makes up the fifth
[the Malayan (12)] . . .; the men throughout being of a
very deep brown colour, with broad nose, and thick hair”
(13). !
“Each of these five principal races contains besides
one or more nations which are distinguished by their
more or less striking structure from the rest of those of
the same division. Thus the Hindoos might be separated
as particular sub-varieties from the Caucasian ; the Chi-
464 Wisconsin Academy of Sciences , Arts and Letters
nese and Japanese from the Mongolian; the Hottentots
from the Ethiopian; so also the North American Indians
from those in the southern half of the new world; and
the black Papuans in New Holland, &c. from the brown
Otaheitans and other islanders of the Pacific Ocean’' (14).
Goldsmith
In a hack work by Oliver Goldsmith (1728-1774) six races
are given.
“If we look round the world, there seems to be not
above six distinct varieties in the human species, each of
which is strongly marked, and speaks the kind seldom to
have mixed with any other” (15).
“I have taken four of these varieties from Linnaeus;
those of the Laplanders and Tartars from Mr. Buffon”
(16).
“The first distinct race of men is found round the
polar regions. The Laplanders, the Esquimaux Indians,
the Samoeid Tartars, the inhabitants of Nova Zembla,
the Borandians, the Greenlanders, and the natives of
Kamtschatka, may be considered as one peculiar race of
people. . . .
“The second great variety in the human species seems
to be that of the Tartar race. . . .
“To this race of men, also, we must refer the Chinese
and the Japanese. . . .
“Another, which makes the third variety in the human
species, is that of the southern Asiatics. . . . The nations
that inhabit the peninsula of India seem to be the princi¬
pal stock. ...
“The fourth striking variety in the human species, is
to be found among the negroes of Africa. . . .
“The inhabitants of America makes a fifth race. . .. .
“The sixth and last variety of the human species, is
that of the Europeans and the nations bordering on them”
(17).
“. . . hair . . . colour differs in different tribes and
races of people. The Americans, and the Asiatics, have
their hair black, thick, straight, and shining. The inhabit¬
ants of the torrid climates of Africa have it black, short,
and woolly. The people of Scandinavia have it red, long,
and curled ; and those of our own and neighboring coun¬
tries, are found with hair of various colours” (18).
“The under jaw in a Chinese face falls greatly more
backward than with us” (19).
Camper
According to Petrus Camper (1722-1789),
Slotlrin — Racial Classifications
465
Table. Camper’s comparative ratios of face breadth.
Vertex-Gnathion: Eurion-Eurion Eurion-Eurion: Zygion-Zygion
Orang
Negro
Calmuck
European
19V2: 14
27:20
32:20
29:23
14:14
20:18
20:24
23:20
From: P. Camper, Works on the Connexion Between The Science
of Anatomy and the Arts of Drawing, Painting, Statuary, &c., Tr.
T. Cogan (London, 1821, New Ed.), 1.5.
“People are distinguished according to the grand divi¬
sions of the continents, into Europeans, Africans, Asi¬
atics, and Americans” (20).
“Having contemplated the inhabitants of various na¬
tions with great attention, I conceived that a striking
difference was occasioned ... by the position of the in¬
ferior maxilla, . . . the breadth of the face, and the quad¬
rangular form of this maxilla” (21).
The first observation led him to the discovery of the facial
angle. For comparative purposes in its investigation, he de¬
veloped the plane which served him as a standard for the meas¬
urement of skulls (22).
“[Camper’s plane:] An horizontal line has been
drawn through the lower part of the nose . . . and the
orifice of the ear . . .; and the . . . skulls were arranged
with care on the line . . . ; attention being also paid to the
direction of the jugale , or cheekbone” (23).
“[Summary on the facial angle:] The two extremi¬
ties ... of the facial lines are from 70 to 100 degrees,
from the negro to the Grecian antique; make it under 70,
and you describe an ourang or an ape ; lessen it still more,
and you have the head of a dog” (24).
On the breadth of the face, he gives comparative ratios which
appear in the table at the end of this article.
Ferguson
Adam Ferguson (1723-1816) made this classification:
“Mankind may be referred to six different races.
“The European , the Samoeide , the Tartar , the Hindoo ,
the Negro, and the American” (25).
466 Wisconsin Academy of Sciences , Arts and Letters
References
1. “Nouvelle division de la terre, par les differentes especes on races d’hom-
mes qui l’habitent,” Journal des Sgavans, 12 (1684), (pp. 148-55) pp. 148-
51; Tr. T. Bendyshe, London, 1863-64.
2. Ibid., pp. 151-55.
3. A Philosophical Account of the Works of Nature (London, 1721), p, 169.
4. He classified man in Sweden as follows:
uClassis I
Quadrupedia
I. Anthropomorpha
Homo
The Men inhabiting Sweden are
a. Goths, of tall stature, hair white and straight, the iris of the eye
ashen blue.
b. Finns, muscular body, hair long and yellow, the iris of the eye
dark.
c. Lapps, small thin body, hair black, straight, short, the iris of the eye
blackish.
d. Variations and mixtures of a. and b. and the others who have
immigrated into Sweden, in the way that may be seen over aill
Europe.” Fauna Suecica (Leyden, 1746), p. 1.
“The young women in Finland have much more swelling bosoms than
those of Lapland.” Iter Lapponicum [1732], p. 181; in Skrifter , ed. Kun-
gliga Svenska Vetenskapsakademien (Upsala, 1905 — ), V; tr. C. Troilus,
rev. J. E. Smith, London, 1811.
5. Pp. 20-32.
0. Vide De Generis Humani Varietate Native , (Gottingen, 1795, 3rd ed)*
4.80; Handbuch der Naturgeschichte [1779] (Gottingen, 12th ed.), pp.
55- 76.
7. (Gottingen, 1776, Reprint of 1st Ed.), pp. 40-42, tr. T. Bendyshe, London,
1865.
8. Vide Abbildungen naturhistorischer Gegenstdnde (Gottingen, 1797-1810).
3, 51.
9. Vide ibid., 1.
10. Vide ibid., 5.
11. Vide ibid., 2.
12. Vide ibid., 4.
13. DGHVN (1781, 2nd ed.); in Anthropological Treatises , tr. T. Bendyshe
(London, 1865), pp. 109-10 n.; vide DGHVN (3rd ed.), 4. 80-89; HN, pp.
56- 57; Beytrdge zur Naturgeschichte (1790-1811) (Gottingen, 1806-11; 1,
2nd ed.), 1. 12.
14. BN, 1. 12.
15. A History of the Earth and Animated Nature [1774] (London, 1853), 2 . 1.
11 (I, p. 232a); Vide idem (I, pp. 237a-238b). ,
16. Ibid., 2. 1. 11 (I, p. 232 n.).
17. Ibid., 2. 1. 11 (I, pp. 232a-236b) .
18. Ibid., 2. 1. 5 (I, p. 202b).
Slotkin — Racial Classifications
467
19. Ibid ^ 2. 1. 5 (I, p. 203a).
20. Works on the Connexion Between the Science of Anatomy and the Arts
of Drawing , Painting , Statuary, &c. [1791] tr. T. Cogan (London, 1821,
new ed.), 11 (p. 14).
Ibid., intr. (p. 8).
Vide ibid., plates 1-3.
Ibid., 1. 3 (p. 33).
Ibid., 1. 3 (p. 42) ; vide ibid., intr; 1. 3-4.
Institutes of Moral Philosophy (Basle, 1800, New Ed.), 1. 1. 4 (alter
Buffon) .
LIST OF PUBLICATIONS DEALING WITH
WISCONSIN LIMNOLOGY
1871-1945
Chancey Juday* and Arthur D. Hasler
Department of Zoology , University of Wisconsin
The publications included in this list deal mainly with the
biology, geology, physics and chemistry of Wisconsin lakes; to
this list have been added the earlier papers of E. A. Birge and
C. Juday, as well as some publications by them based on obser¬
vations of lakes situated in other states and countries.
The great majority of these books and papers has come from
the Limnological Laboratory of the Wisconsin Geological and
Natural History Survey, and from the department of Zoology,
University of Wisconsin. Other departments of the University
which contributed richly are: Botany, Agricultural Bacteriolo¬
gy, Chemistry, Physics, and Geology. A considerable number are
the result of investigations carried on in cooperation with the
U. S. Bureau of Fisheries, now a division of the Fish and Wild¬
life Service, the Wisconsin Conservation Department, the Uni¬
versity of Michigan, the University of Illinois, the University of
Minnesota, and the Works Progress Administration. Assistance
in preparing some of the material for publication has also been
received from the National Youth Administration. Much finan¬
cial assistance for some of the projects has been received from
the Brittingham Trust Fund and from the Wisconsin Alumni
Research Foundation.
Bibliography
Allgeier, R. J., Halford, B. C. and Juday, C. 1941. Oxidation-reduction poten¬
tials and pH of lake waters and lake sediments. Trans. Wisconsin Acad.
Sci. 33: 115-133.
Allgeier, R. J., Peterson, W. H., and Juday, C. 1934. Availability of carbon in
certain aquatic materials under aerobic conditions of fermentation. In-
temat. Rev. ges. Hydrobiol. u. Hydrog. 30: 371-378.
Allgeier, R. J., Peterson, W. H., Juday, C., and Birge, E. A. 1932. The anaero¬
bic fermentation of lake deposits. Ibid. 26: 444-461.
•Deceased (March 29, 1944).
469
470 Wisconsin Academy of Sciences , Arts and Letters
Andrews, Jay D., and Hasler, A. D. 1943. Fluctuations in the animal popula¬
tions of the littoral zone in Lake Mendota. Trans. Wisconsin Acad Sci
35: 175-185.
Andrews, O. V. 1920. An ecological survey of Lake Butte des Moris Bog,
Oshkosh, Wis. Bull. Wis. Nat. Hist. Soc. 13 (N.S.): 196-211.
Baker, Frank Collins. 1914. The molluscan fauna of Tomahawk Lake, Wis¬
consin, with special reference to its ecology. Trans. Wisconsin Acad. Sci.
17: 200-246.
- 1922. New Lymnaeas from Wisconsin and Minnesota with
notes on shells from the latter state. Nautilus 36: 22-25.
— — - 1922. New species and varieties of Mollusca from Lake
Winnebago, Wisconsin, with new records from this state. Ibid. 35: ISO-
133; 36: 19-21.
- 1924. The fauna of the Lake Winnebago region; a quanti¬
tative and qualitative survey with special reference to the Mollusca.
Trans. Wisconsin Acad. Sci. 21: 109-146.
- - 1926. Nomenclatorial notes on American freshwater Mol¬
lusca. Ibid. 22: 193-205.
- 1928. The freshwater Mollusca of Wisconsin. Part I. Gas¬
tropoda. xx-507 pp., 28 plates; Part II. Pelecypoda. vi-495 pp., 77 plates.
Bull. No. 70, Wis. Geol. and Nat. Hist. Survey & Bull. No. 1527, University
of Wisconsin. Published jointly by the Wisconsin Acad. Sci., the Univer¬
sity of Wisconsin and the Wis. Geol. and Nat. Hist. Survey.
Bennett, George W. 1937. The growth of the large -mouthed black bass in
the waters of Wisconsin. Copeia 1937: 104-118.
- - 1938. Growth of the small-mouthed black bass in Wiscon¬
sin waters. Ibid. 1938: 157-170.
Bere, Ruby. 1931. Copepods parasitic on fish of the Trout Lake region, with
descriptions of two new species. Trans. Wisconsin Acad. Sci. 26: 427-436.
- 1931. Leeches from the lakes of northeastern Wisconsin.
Ibid. 26:437-440.
- 1933. Numbers of bacteria in inland lakes of Wisconsin as
shown by the direct microscopic method. Internatl. Rev. ges. Hydrobiol.
u. Hydrog. 29:248-263.
— - 1935. Further notes on the occurrence of parasitic copepods
on fish of the Trout Lake region, with a description of the male of
Argulus biramosus. Trans. Wisconsin Acad. Sci. 29: 83-88.
Birge, E. A. 1873. The ant-lion. American Naturalist 7: 432.
— - 1879. Notes on Cladocera. Trans. Wisconsin Acad. Sci. 4:
77-112.
- - — 1881. Notes on the functions of the spinal cord in the frog.
Amer. Micros. Jour. 2: 210-213.
— — - — - 1882. On a convenient method of embedding. Ibid. 3: 73-75.
- — - - 1882. On the first zoea stage of Pinnotheres ostreum,
American Naturalist 16: 589-591.
— - 1882. tJber die Reizbarkeit der motorischen Ganglienzelless
des Ruckenmarks. Arch. f. Anat. u. Physiol. (Physiol. Abt.) 1882: 481-
489.
Juday and Hasler — Wisconsin Limnology Publications 471
— - - — 1882. Die Zahl der Nervenfasern und der motorischen
Ganglienzellen im Ruckenmark des Frosches. Ibid. 1882: 435-480.
— - — - 1883. Notes on the development of Panopaeus sayi Smith.
Johns Hopkins Univ. Biol. Lab. Studies 2: 411-426.
- - — 1885. On the motor ganglion cells of the frog’s spinal cord.
Trans. Wisconsin Acad. Sci. 6: 51-81.
- - - - — 1892. Notes and list of Crustacea Cladocera from Madison,
Wisconsin. Ibid. 8: 379-398.
- - — - - - 1893. Notes on Cladocera, HI. Ibid. 9: 275-317.
— - — — — 1894. The Cladocera. Bull. Mich. Fish. Com. No. 4: 45-47.
- - - 1895. Cladocera (of Turkey Lake, Indiana). Proc. Ind
Acad. Sci. 5: 244-246.
- - 1895. On the vertical distribution of the pelagic Crustacea
of Lake Mendota, Wisconsin, during July, 1894. Biol. Centralbl. 15: 353-
355.
— — - 1897. The vertical distribution of the limnetic Crustacea of
Lake Mendota. Ibid. 17: 371-374.
— - 1898. Plankton studies on Lake Mendota. 2. The Crustacea
of the plankton from July, 1894, to December, 1896. Trans. Wisconsin
Acad. Sci. 11: 274-448.
- - 1901. The cone net. Jour. Applied Micros. 4: 1405-1407.
- - - 1901. Report of Limnological Commission. Trans. Amer.
Micros. Soc. 22: 193-196.
- - 1904. A biological reconnaissance of some elevated lakes
in the Sierras and Rockies. (H. B. Ward) Report on the Cladocera.
Studies Zool. Lab. Univ. Nebr. No. 60: 149-152.
— - 1904. The thermocline and its biological significance. Trans.
Amer. Micros. Soc. 25: 5-32.
- 1907. Gases dissolved in the waters of Wisconsin lakes.
Trans. Amer. Fish. Soc. 1906: 142-163. (Reprinted in Rept. Wis. Com¬
missioners of Fisheries, pp. 118-139, and in Proc. of Fourth Internat. Fish.
Cong. Part II: 1273-1292, 1908.)
- — 1907. The respiration of an inland lake. Ibid. 1907: 223-
241. Also Pop. Sci. Mo. 72: 337-351. 1908.
— - - 1910. The apparent sinking of ice in lakes. Science, N.S.
32: 81-82.
— - - 1910. Notes on Cladocera IV. Trans. Wisconsin Acad. Sci.
16: 1017-1066.
- 1910. On the evidence of temperature seiches. Ibid. 16:
1005-1016.
- — 1910. An unregarded factor in lake temperatures. Ibid.
16: 989-1004.
— - - - 1913. Absorption of the sun’s energy by lakes. Science 38:
702-704.
- - — 1915. The heat budgets of American and European lakes.
Trans. Wisconsin Acad. Sci. 18: 166-213.
t— — - - 1916. The work of the wind in warming a lake. Ibid. 18:
341-391,
172 Wisconsin Academy of Sciences , Arts and Letters
- 1918. The water fleas (Cladocera). In Ward & Whipple’s
Freshwater Biology, pp. 676-740.
- 1922. A second report on limnological apparatus. Trans.
Wisconsin Acad. Sci. 20: 533-552.
- 1923. The plankton of the lakes. Trans. Amer. Fisheries
Soc. 52: 118-130.
- 1929. Fish and their food. Ibid. 59: 188-194.
- 1936. Biology of Lake Mendota. Technical Club of Madison.
1936: 11-12.
Birge, E. A., and Juday, C. 1908. A summer resting stage in the development
of Cyclops biscuspidatus Claus. Trans. Wisconsin Acad. Sci. 16: 1-9.
- 1911. The inland lakes of Wisconsin. I. The dissolved
gases and their biological significance. Bulletin, Wis. Geol. and Nat. Hist.
Survey 22: 259 pp.
- 1914. a limnological study of the Finger Lakes of New
York. Bull. U. S. Bureau Fisheries 32: 525-609.
- 1920. A limnological reconnaissance of West Okoboji. Univ.
Iowa Studies Nat. Hist. 9: 1-56.
- 1921. Further limnological observations on the Finger
Lakes of New York. Bull. U. S. Bureau Fisheries 37: 211-252.
- 1922. The inland lakes of Wisconsin. The plankton. L Its
quantity and chemical composition. Bulletin, Wis. Geol. and Nat. Hist.
Survey No. 64: (Scientific series 13), ix-222 pp.
- 1926. Organic content of lake water. Bull. U. S. Bureau of
Fisheries 42: 185-205.
- 1926. The organic content of lake water. Proc. Nat. Acad.
Sci. 12: 518-519.
- 1927. The organic content of the water of small lakes.
Proc. Amer. Phil. Soc. 66: 357-372.
■ - 1929. Penetration of solar radiation into lakes as measured
by the thermopile. Bull. Nat. Res. Counc. No. 68. Trans. Amer. Geophys.
Union, 9th Ann. Meeting, pp. 61-76.
- 1929. Transmission of solar radiation by the waters of
inland lakes. Trans. Wisconsin Acad. Sci. 24: 509-580.
- 1930. A second report on solar radiation and inland lakes.
Ibid. 25: 285-335.
- 1931. A third report on solar radiation and inland lakes.
Ibid. 26: 383-425.
- 1932. Solar radiation and inland lakes. Fourth Report.
Observations of 1931. Ibid. 27: 523-562.
- - 1934. Particulate and dissolved organic matter in inland
lakes. Ecol. Monog. 4: 440-474.
B*rge, E. A., Juday, C., and March, H. W. 1928. The temperature of the
bottom deposits of Lake Mendota: A chapter in the heat exchange of the
lakes. Trans. Wisconsin Acad. Sci. 23: 187-231.
Birge, E. A., Olson, O. A., and Harder, H. P. 1895. Plankton studies on Lake
Mendota. I. The vertical distribution of the pelagic Crustacea during
1894. Ibid. 10: 421-484.
i
Juday and Hasler — Wisconsin Limnology Publications 478
Birge, E. A., and Rich, W. H. 1927. Observations on Karluk Lake, Alaska.
Ecology 8:384.
Black, C. S. 1929. Chemical analyses of lake deposits. Trans. Wisconsin Acad.
Sci. 24: 127-133.
Brackett, Sterling. 1940. Studies on Schistosome dermatitis. V. Prevalence in
Wisconsin. Amer. Jour. Hyg. 31(3): 49-63.
- — — — — 1940. Studies on Schistosome dermatitis. VIII. Notes on
the biology of the snail hosts of schistosome cercariae in Wisconsin and
epidemiological evidence for the life cycles of some avian schistosomes.
Amer. Jour. Hyg. 32: 85-104.
- - — _ 1940. Two new species of schistosome cercariae from Wis¬
consin. Jour. Parasitol. 26(3): 195-200.
- - 1940. Two new species of strigeid cercariae in Lymnaeid
snails from the United States. Ibid. 25 (3) : 263-268.
Broughton, W. A. 1941. The geology, ground water and lake basin seal of the
region south of the Muskellunge Moraine, Vilas County, Wisconsin. Trans.
Wisconsin Acad. Sci. 33: 5-20.
Buckley, Ernest Robertson. 1901. Ice ramparts. Ibid. 13: 141-162.
Bundy, W. F. 1883. The crustacean fauna of Wisconsin, with descriptions of
little known species of Cambarus. Geol. of Wis. 1: 402-405.
Carpenter, Phillip L. 1939. Bacterial counts in the muds of Crystal Lake —
an oligo trophic lake of northern Wisconsin. Jour. Sedim. Petrol. 9: 3-7.
April.
Chase, Wayland Johnson, and Noland, Lowell E. 1927. The history and hydro¬
graphy of Lake Ripley (Jefferson County, Wisconsin). Trans. Wisconsin
Acad. Sci. 23: 179-186.
Clarke, George L., and James, Harry R. 1939. Laboratory analysis of the
selective absorption of light by sea water. Jour. Optic. Soc. Amer. 29:
43-55.
Conger, Paul S. 1939. The contribution of diatoms to the sediments of
Crystal Lake, Vilas County, Wisconsin. Amer. Jour. Sci. 237: 324-340.
May.
- 1939. Origin and utilization of diatomaceous peat deposits.
Scientific Monthly 49: 509-523.
- - — 1942. Accumulation of diatomaceous deposits. Jour. Sedim.
Petrol. 12: 55-66.
Couey, F. M. 1935. Fish food studies of a number of northeastern Wisconsin
lakes. Trans. Wisconsin Acad. Sci. 29: 131-172.
Creaser, Edwin P. 1932. The decapod crustaceans of Wisconsin. Ibid. 27:
321-338.
Cross, S. X. 1934. A probable cause of non-specific immunity between two
parasites of ciscoes of the Trout Lake region of northern Wisconsin.
Jour. Parasitol. 20: 244-245.
- _____ — _ 1935. The effect of parasitism on the growth of perch in
the Trout Lake region. Ibid. 21: 267-273.
- - 1938. A study of the fish parasite relationships in the
Trout Lake region of Wisconsin. Trans. Wisconsin Acad. Sci. 31: 439-456.
Curtis, John T., and Juday, C. 1937. Photosynthesis of algae in Wisconsin
474 Wisconsin Academy of Sciences, Arts and Letters
lakes. III. Observations of 1935. Internatl. Rev. ges. HydrobioL u. Hydrog.
35: 122-133.
Davis, Francis J. 1941. Surface loss of solar and sky radiation by inland
lakes. Trans. Wisconsin Acad. Sci. 33: 83-93.
Denniston, Rollin Henry. 1921. A survey of the larger aquatic plants of Lake
Mendota. Ibid. 20: 495-500.
Deutsch, H. F., and Hasler, A. D. 1943. Distribution of a vitamin Bi destruc¬
tive enzyme in fish. Proc. Soc. Exptl. Biol, and Med. 53: 63-65.
Dickinson, W. E. 1936. The mosquitoes of Wisconsin. Bull. Pub. Museum,
Milwaukee 8: No. 3.
Domogalla, B. P., and Fred, E. B. 1926. Ammonia and nitrate studies of lakes
near Madison, Wisconsin. Jour. Amer. Soc. Agron. 18: 897-911.
Domogalla, B. P., Fred, E. B., and Peterson, W. H. 1926. Seasonal variations
in the ammonia and nitrate content of lake waters. Jour. Amer. Water
Works Assoc. 15: 369-385.
Domogalla, B. P., Juday, C., and Peterson, W. H. 1925. The forms of nitrogen
found in certain lake waters. Jour. Biol. Chem. 63: 269-285.
Dutton, Herbert, and Juday, C. 1944. Chromatic adaptation in relation to
color and depth distribution of freshwater phytoplankton and large
aquatic plants. Ecology 25: 273-282.
Dutton, Herbert J., and Manning, W. M. 1941. Evidence for carotenoid-sensi¬
tized photosynthesis in the diatom Nitzschia closterium . Amer. Jour.
Bot. 28: 516-526.
Edmundson, W. T. 1840. The sessile Rotatoria of Wisconsin. Trans. Amer.
Micros. Soc. 59: 433-459.
Enteman, Minnie Marie. 1900. Variations in the crest of Daphnia hyalina.
Amer. Naturalist 34: 879-890.
Erikson, Dagny. 1941. Studies on some lake-mud strains of Micromonospora.
Jour. Bact. 41: 277-300.
Fassett, N. C. 1930. The plants of some northeastern Wisconsin lakes. Trans.
Wisconsin Acad. Sci. 25: 155-168.
— _ - 1940. A manual of aquatic plants. McGraw-Hill, N. Y.
382 pp.
Fenneman, N. M. 1902. On the lakes of southeastern Wisconsin. Wis. Geol
and Nat. Hist. Survey, Bull. No. 8, 178 pp. Reprinted in 1910.
Field, John B., Elvehjem, C. A., and Juday, C. 1943. A study of the blood
constituents of carp and trout. Jour. Biol. Chem. 148: 261-269.
Field, John B., Gee, Lynn L., Elvehjem, C. A., and Juday, C. 1944. The blood
picture in furunculosis induced by Bacterium salmonicida in fish. Arch.
Biochem. 3: 277-284.
Field, John B., Herman, Elmer F., and Elvehjem, C. A. 1944. Increased
growth produced by gelatin in trout fed meatless diets. Proc. Soc. ExptL
Biol, and Med. 55: 222-225.
Flanigon, Thomas H. 1942. Limnological observations on three lakes in east¬
ern Vilas County, Wisconsm. Trans. Wisconsin Acad. Sci. 34: 167-175.
Fred, E. B., Wilson,- F. C., and Davenport, Audrey. 1924. The distribution and
significance of bacteria in Lake Mendota. Ecology 5: 322-339. October.
Juday and Easier— Wisconsin Limnology Publication® 475
Freeman, S., Meloche, V. W., and Juday, C. 1933. The determination ©I the
hydrogen ion concentration of inland lake waters. Internatl. Rev. ges.
Hydrobiol. u. Hydrog. 30: 346-359.
Frey, David Grover. 1940. Growth and ecology of the carp, Cyprinm carpio ,
Linnaeus, in four lakes of the Madison region, Wisconsin. Manuscript
Ph. D. Thesis. 248 pp. Library, University of Wisconsin.
- 1942. Annulus formation in the scales of the carp. Copeia,
1942: 214-223.
Frey, D. G., and Pedracine, H. 1938. Growth of the buffalo in Wisconsin
lakes and streams. Trans. Wisconsin Acad. Sci. 31: 513-525.
Frey, David G., Pedracine, Hubert, and Vike, Lawrence. 1939. Results of a
summer creel census of Lakes Waubesa and Kegonsa, Wisconsin. Jour.
Wildlife Management 3: 243-254. July.
Frey, David G., and Vike, Lawrence. 1941. A creel census on Lakes Waubesa
and Kegonsa, Wisconsin, in 1939. Trans. Wisconsin Acad. Sci. 33: 339-362.
Fries, Carl, Jr. 1938. Geology and ground water of the Trout Lake region.
Vilas County, Wisconsin. Ibid. 31: 305-322.
Gee, Lynn L., and Sarles, W. B. 1942. The disinfection of trout eggs con¬
taminated with Bacterium salmonicida. Jour. Bact. 44: 11-126.
Gifford, Elizabeth M., and Peckham, Geo. W. 1882. Temperature of Pine,
Beaver and Okauchee lakes. Trans. Wisconsin Acad. Sci. 5: 273-275.
Greene, C. W. 1926. An ichthyological survey of Wisconsin. Papers Mich.
Acad. Sci., Arts and Let. 7: 299-310.
- 1935. The distribution of Wisconsin fishes. Wisconsin Con¬
servation Department. 235 pp.
Hardman, Yvette. 1938. Some filamentous bacteria from Wisconsin lakes. A
thesis submitted to the faculty of the Graduate School of the University
of Minnesota for M.S. degree. June, 1938. 25 pp. Ms.
— - - - 1941. The surface tension of Wisconsin lake waters. Trans.
Wisconsin Acad. Sci. 33: 395-404.
Hardman, Yvette, and Henrici, Arthur T. 1939. The distribution of Sidero-
capsa treubii in some lakes and streams. Jour. Bact. 37: 97-104. January.
Harring, H. K., and Myers, F. J. 1922. The rotifers of Wisconsin. Trans.
Wisconsin Acad. Sci. 20: 553-662.
— - - 1924. The rotifer fauna of Wisconsin. II. A revision of the
notommatid rotifers, exclusive of the Dicranophorinae. Ibid. 21: 514-549.
— - 1926. The rotifer fauna of Wisconsin. III. A revision of the
genera Lecane and Monostyla. Ibid. 22: 315-423.
- 1927. The rotifer fauna of Wisconsin. IV. The Dicrano¬
phorinae. Ibid. 23: 667-808.
Hasler, A. D. 1935. The physiology of digestion of plankton Crustacea. Biol.
Bull. 68: 207-214.
- - - 1937. The physiology of digestion in plankton Crustacea.
II. Further studies in the digestive enzymes of (A) Daphnia and Poly¬
phemus and (B) Diaptomus and Calanus. Ibid. 72: 290-298.
— - - 1945. Observations on the winter perch populations of
Lake Mendota. Ecology 26: 90-94.
476 Wisconsin Academy of Sciences , Arts and Letters
Hasler, Arthur D., and Faber, Wm. M. 1941. A tagging method for small fish.
Copeia, 1941: 162-165.
Hasler, A. D., and Meyer, Boland K. 1942. Respiratory responses of normal
and castrated goldfish to teleost and mammalian hormones. Jour. Exptl.
Zool. 91: 391-404.
Hasler, A. D., Meyer, R. K., and Field, H. M. 1939. Spawning induced pre¬
maturely in trout with the aid of pituitary glands of the carp. Endo¬
crinology 25: 978-983.
- 1940. The use of hormones for the conservation of muskel-
lunge, Esox masquinongy immaculatus Garrard. Copeia, 1940: 43-46.
Hathaway, E. S. 1927. Quantitative study of the changes produced by accli¬
matization in the tolerance of high temperatures by fishes and amphibians.
Bull. U. S. Bureau Fisheries 48: 169-192.
- 1927. The relation of temperature to the quantity of food
consumed by fishes. Ecology 8: 428-434.
Henrici, A. T., and McCoy, Elizabeth. 1938. The distribution of heterotrophic
bacteria in the bottom deposits of some lakes. Trans. Wisconsin Acad. Sci.
31: 323-36L
Higley, W. K. 1889. Reptilia and Batrachia of Wisconsin. Ibid. 7: 155-176.
Hile, R. 1936. Age and growth of the Cisco, Leucichthys artedi (Le Sueur),
in the lakes of northeastern Highlands, Wisconsin. Bull. U. S. Bureau
Fisheries 48: 211-317.
- 1936. Summary of investigations on the morphometry of
the Cisco, Leucichthys artedi (Le Sueur), in the lakes of the northeastern
Highlands, Wisconsin. Papers Mich. Acad. Sci., Arts and Let. 21: 619-634.
- 1937. Morphometry of the Cisco, Leucichthys artedi (Le
Sueur), in the lakes of northeastern Highlands, Wisconsin. Internatl.
Rev. ges. Hydrobiol. u. Hydrog. 36: 57-130.
- 1941. Age and growth of the rock bass, Ambloplites rupes-
tris (Rafinesque) , in Nebish Lake, Wisconsin. Trans. Wisconsin Acad. Sci.
33: 189-337.
- 1942. Growth of the rock bass, Ambloplites rupestris (Ra¬
finesque), in five lakes of northeastern Wisconsin. Trans. Amer. Fisheries
Soc. 71: 131-143.
- 1942. Mathematical relationship between the length and
age of the rock bass, Ambloplites rupestris (Rafinesque). Papers Mich.
Acad. Sci., Arts and Let. 28: 331-341.
Hile, Ralph, and Deason, Hilary J. 1935. Growth of the whitefish, Coregonus
clupeajormis (Mitchill), in Trout Lake, northeastern Highlands, Wiscon¬
sin. Trans. Amer. Fisheries Soc. 64: 231-237.
Hile, Ralph, and Juday, C. 1941. Bathymetric distribution of fish in lakes of
northeastern Highlands, Wisconsin. Trans. Wisconsin Acad. Sci. 33: 147-
187.
Holmes, Samuel Jackson. 1909. Description of new subterranean amphipod
from Wisconsin. Ibid. 16: 77-80.
_ _ 1910. Description of a new species of Eubranchipus from
Wisconsin with observations on its reaction to light. Ibid. 16: 1252-1255.
Hoy, P. R. 1871. Abstracts of a paper on the fauna of Lake Michigan off
Racine. Ibid. 2: 34-35.
Juday and Hasler — Wisconsin Limnology Publications 477
- 1872. Deep-water fauna of Lake Michigan. Ibid. 1: 98-101.
- — - - — 1872. Mortality of fish in the Racine River. Proc. Amer,
Assoc. Adv. Sci. 1872: 198-199.
- 1876. Fish culture. Trans. Wisconsin Acad. Sci. 3: 37-39.
- - - - 1876. On the extent of the Wisconsin fisheries. (An ab¬
stract of notes sent by Dr. Hoy.) Ibid. 3 : 65-67.
- 1877. Catalogue of the cold-blooded vertebrates of Wis¬
consin. Geol. Surv. Wis. 1873-1879. Vol. I, Part 2; Chap. 9: 422-435.
- - 1882. Water puppy, ( Menobranchus lateralis Say). Trans.
Wisconsin Acad. Sci. 5: 248-250.
Hubbs, C. L., and Greene, C. W. 1935. Two new sub-species of fishes from
Wisconsin. Ibid. 29: 89-101.
Jackson, H. H. T. 1912. A contribution to the natural history of the amphi-
pod, Hyalella knickerbockeri Bate. Bull. Wis. Nat. Hist. Soc. 10: 49-60.
James, Harry R., and Birge, E. A. 1938. A laboratory study of the absorption
of light by lake waters. Trans. Wisconsin Acad. Sci. 31: 1-154.
Jewell, Minna E. 1935. An ecological study of the fresh-water sponges of
northern Wisconsin. Ecol. Monog. 5: 461-504.
- 1939. An ecological study of the fresh-water sponges of
Wisconsin. II. The influence of calcium. Ecology 20: 11-28.
Juday, C. 1896. Hydrographic map of Turkey Lake. Proc. Ind. Acad. Sci.
(Frontispiece) 1895.
- — — - - 1897. The plankton of Turkey Lake. Ibid. 1896: 287-296.
- - 1903. The plankton of Winona Lake. Ibid. 1902: 120-133.
- - — 1904. The diurnal movement of plankton Crustacea. Trans.
Wisconsin Acad. Sci. 14: 534-568.
- - - 1904. Fishes of Boulder County, Colorado. Univ. of Colo.
Studies 2: 113-114.
- 1905. List of fishes collected in Boulder County, Colorado,
with description of a new species of Leuciscus. Bull. U. S. Bureau Fish¬
eries 24: 223-227.
- - 1906. The food of the trout of the Kern River region. Ibid „
25: 43-49.
- 1906. Ostracoda of the San Diego region. I. Haloeypridae„
Univ. Calif. Pub. Zool. 3: 13-38.
- - 1907. Cladocera of the San Diego region. Ibid. 3: 157-158.
- - 1907. Notes on Lake Tahoe, its trout and trout-fishing.
Bull. U. S. Bureau Fisheries 26: 137-146.
- 1907. Ostracoda of the San Diego region, n. Littoral forms.
Univ. Calif. Pub. Zool. 3: 135-156.
- - 1907. Studies on some lakes in the Rocky and Sierra
Nevada Mountains. Trans. Wisconsin Acad. Sci. 15: 781-793.
- - - 1907. A study of Twin Lakes, Colorado, with especial con¬
sideration of the food of the trouts. Bull. U. S. Bureau Fisheries 26:
147-178.
- - 1908. Resume of recent work on lakes by the Wisconsin
Geological and Natural History Survey. Intematl. Rev. ges. Hydrobiol. u.
Hydrog. 1: 240-242.
478 Wisconsin Academy of Sciences , Arts and Letters
- - - 1908. Some aquatic invertebrates that live under anaerobic
conditions. Trans. Wisconsin Acad. Sci. 16: 10-16.
- 1910. Some European biological stations. Ibid. 16: 1257-
1277.
- 1913. Air in the depths of the ocean. Science, N.S. 38:
546-547.
- 1914. The inland lakes of Wisconsin. II. The hydrography
and morphometry of the lakes. Wis. Geol. and Nat. Hist. Survey Bulletin
27: xv-137pp.
- 1914. A new species of Diaptomus. Trans. Wisconsin Acad.
Sci. 17: 803-805.
- 1915. Limnological studies on some lakes in Central Amer¬
ica. Ibid. 18: 214-250.
- 1916. Horizontal rainbows on Lake Mendota. Monthly
Weather Review 44: 65-67.
- 1916. Limnological apparatus. Trans. Wisconsin Acad. Sci.
18: 566-592.
- 1919. A freshwater anaerobic ciliate. Biol. Bull. 36: 92-95.
- 1920. Cladocera. Report of Canadian Arctic Expedition
1913-1918, 7: Part H, pp. 1-8.
- 1920. Horizontal rainbows. Science, N.S., 51: 188.
- 1920. The plankton of Lake Maxinkuckee. In “Lake Max-
inkuckee. A physical and biological survey.” By B. W. Evermann and
H. W. Clark. II: 105-110. Department of Conservation, State of Indiana.
See also: Trans. Amer. Micros. Soc. 23: 61-62. 1902.
- 1921. Observations on the larva of Corethra punctipennis
Say. Biol. Bull. 40: 271-286.
- 1922. Limnological observations on Lake George. A bio¬
logical survey of Lake George, New York. N. Y. Cons. Comn. 1921,
pp. 37-51.
- - - 1922. Quantitative studies of the bottom fauna in the
deeper waters of Lake Mendota. Trans. Wisconsin Acad. Sci. 20: 461-493.
- 1923. An interesting copepod from the Finger Lakes, New
York. Science 58: 205.
- 1923. The water-fleas. In “A scientific survey of Turners
Lake, Isle-au-Haut, Maine.” N. Y. State Museum. August. Published
privately, pp. 16-17.
- 1924. The productivity of Green Lake, Wisconsin. Ver-
handl. Internatl. Ver. f. Limnol. 2: 357-360.
- 1924. Summary of quantitative investigations on Green
Lake, Wisconsin. Internatl. Rev. ges. Hydrobiol. u. Hydrog. 12: 1-12.
- 1925. Sencella calanoides , a recently described freshwater
copepod. Proc. U. S. Nat. Mus. 66: 1-6.
- 1926. Freshwater Cladocera from southern Canada. Ca¬
nadian Field Nat. 40: 99-100.
- 1926. Sand flotation on lakes. Science, N.S., 64: 138.
- 1926. A third report on limnological apparatus. Trans.
Wisconsin Acad. Sci. 22: 299-315.
Juday and Hosier— Wisconsin Limnology Publications 479
— — — - - — 1927. Freshwater Cladocera from the east shore of Hudson
and James bays. Canadian Field Nat. 41: 130-131.
- - - - 1929. Limnological methods. Arch. f. Hydrobiol. 20: 517-
524.
- — - - 1934. The depth distribution of some aquatic plants. Ecol¬
ogy 15: 325.
- - - 1934. Growth of game fish. Field and Stream, December,
1934: 7-72.
- - - - — — 1935. Chemical composition of large aquatic plants. Sci¬
ence 81: 273.
- - - 1937. Trout Lake. The Limnological Laboratory. The Biol¬
ogist 18: 177-182. March-May.
- — — - 1938. Fish records for Lake Wingra. Trans. Wisconsin
Acad. Sci. 31: 533-534.
- — - - 1938. Wisconsin lakes and fish investigations. Prog. Fish
Cult., June-July, 1938. No. 39: 18-21.
- - — - — 1940. The annual energy budget of an inland lake. Ecology
21: 438-450.
- 1943. The summer standing crop of plants and animals in
four Wisconsin lakes. Trans. Wisconsin Acad. Sci. 34: 387-410.
- — - - — 1943. The utilization of aquatic food resources. Science 97
(2525): 456-458.
Juday, C., and Bennett, G. W. 1935. The growth of game fish in Wisconsin
waters. Mimeographed report, 13 pp.
Juday, C., and Birge, E. A. 1927. Pontoporeia and Mysis in Wisconsin lakes.
Ecology 8: 445-452.
- — - — 1930. The highland lake district of northeastern Wisconsin
and the Trout Lake limnological laboratory. Trans. Wisconsin Acad. Sci.
25: 337-352.
- - - - 1931. A second report on the phosphorus content of Wis¬
consin lake waters. Ibid. 26: 353-382.
- 1932. Dissolved oxygen and oxygen consumed in the lake
waters of northeastern Wisconsin. Ibid. 27: 415-486.
- — - — — 1933. The transparency, the color and the specific con¬
ductance of the lake waters of northeastern Wisconsin. Ibid. 28: 205-259.
- - 1941. Hydrography and morphometry of some northeastern
Wisconsin lakes. Ibid. 33: 21-72.
Juday, C., Birge, E. A., and Kemmerer, G. I. 1927. Phosphorus content of
lake waters of northeastern Wisconsin. Ibid. 23: 233-248.
Juday, C., Birge, E. A., and Meloche, V. W. 1935. The carbon dioxide and
hydrogen ion content of the lake waters of northeastern Wisconsin. Ibid.
29: 1-82.
- 1938. Mineral content of the lake waters of northeastern
Wisconsin. Ibid. 31: 223-276.
- - 1941. Chemical analyses of bottom deposits of Wisconsin
lakes. II. Second report. Ibid. 33: 99-114.
Juday, C., Blair, J. Morris, and Wilda, E. F. 1943. The photosynthetic activi¬
ties of the aquatic plants of Little John Lake, Vilas County, Wisconsin.
Amer. Midland Nat. 30: 426-446.
480 Wisconsin Academy of Sciences , Arts and Letters
Juday, C., Fred, E. B., and Wilson, F. C. 1924. The hydrogen ion concentra¬
tion of certain Wisconsin lake waters. Trans. Amer. Micros. Soc. 43:
177-190.
Juday, C., Livingston, Clarence, and Pedracine, Hubert. 1938. A census of
the fish caught by anglers in Lake Waubesa in 1937. Mimeographed re¬
port, 7 pp. January.
Juday, C., and Meloche, V. W. 1944. Physical and chemical evidence relating
to the lake basin seal in certain areas of the Trout Lake region of Wis¬
consin. Trans. Wisconsin Acad. Sci. 35: 157-174.
Juday, C., and Muttkowski, R. 1915. Entomostraca of St. Paul Island, Alaska.
Bull. Wis. Nat. Hist. Soc. 13: 23-31.
Juday, C., Rich, W. H., Kemmerer, G. I., and Mann, A. 1932. Limnological
studies of Karluk Lake, Alaska, 1926-1930. Bull. U. S. Bureau Fisheries
47: 407-436.
Juday, C., and Schloemer, C. L. 1936. Growth of game fish in Wisconsin
waters. Fourth report. Mimeographed form. 17 pp.
- 1938. Effect of fertilizers on plankton production and on
fish growth in a Wisconsin lake. Prog. Fish Cult. 40: 24-27. August-
September.
- 1938. Growth of game fish in Wisconsin waters. Fifth re¬
port. Limn. Lab. Wis. Geol. and Nat. Hist. Survey. 26 pp.
Juday, C., and Schneberger, E. 1930. Growth studies of game fish in Wis¬
consin waters. Mimeographed report. 7 pp.
- 1933. Growth studies of game fish in Wisconsin waters.
Second report. Mimeographed report. 10 pp.
Juday, C., and Schomer, H. A. 1935. The utilization of solar radiation by
algae at different depths in lakes. Biol. Bull. 69: 75-81.
Juday, C., and Vike, L. E. 1938. A census of the fish caught by anglers in
Lake Kegonsa. Trans. Wisconsin Acad. Sci. 31: 527-532.
Juday, C., and Wagner, G. 1808. Dissolved oxygen as a factor in the distribu¬
tion of fishes. Ibid. 16: 17-22.
Kemmerer, G. I., and Halle tt, L. T. 1927. An improved method of organic
microcombustion. Indust, and Eng. Chem. 19: 173-176.
- 1927. Improved micro-Kjeldahl ammonia distillation ap¬
paratus. Ibid. 19: 1295-1296.
- 1927. Micro determination of carbonate carbon. Ibid. 19:
1352-1354.
Kozminski, Zygmunt. 1937. The lake district of northeastern Wisconsin.
Translated by J. A. Birkenmajer from an article in Polish in Wszechswiata
(The Universe), No. 8.
- 1938. Amount and distribution of the chlorophyll in some
lakes of northeastern Wisconsin. Trans. Wisconsin Acad. Sci. 31: 411-438.
- 1938. Ueber die Chlorophyllverteilung in einigen Seen von
Nordost-Wisconsin (U.S.A.). Archiv. Hydrob. et Ichthyol. XI: 143-165.
Knudson, Harold W., Juday, C., and Meloche, V. W. 1940. Silicomolybdate
method for silica. Indus, and Eng. Chem., Anal. Ed. 12: 270-273.
Knudson, Harold W., Meloche, V. W., and Juday, C. 1940. Colorimetric
analysis of a two-component color system. Ibid. 12: 715-718.
Juday and Easier — Wisconsin Limnology Publications 481
Lapham, Increase A. 1872. Oconomowoc Lake, and other small lakes of
Wisconsin, considered with reference to their capacity for fish-production.
Trans. Wisconsin Acad. Sci. 3: 31-36.
Lehmann, Harriet. 1903. Variations in form and size of Cyclops brevispinosus
Herrick and Cyclops americanus Marsh. Ibid. 14: 279-298.
Lohuis, D., Meloche, V. W., and Juday, C. 1938. Sodium and potassium con¬
tent of Wisconsin lake waters and their residues. Ibid. 31: 285-304.
McKelvey, V. E. 1940. Beach sediments of Trout Lake, Wisconsin. Jour.
Sedim. Petrol. 10: 65-77.
- - - 1941. The flotation of sand in nature. Amer. Jour. Sci.
239: 594-607. August.
Manning, W. M. 1938. Photosynthesis. Jour. Phys. Chem. 42 (6): 815-854.
- 1940. A method for obtaining continuous records of dis¬
solved oxygen in lakes. Ecology 21: 509-512.
- - 1943. Physical factors influencing the accuracy of the drop¬
ping mercury electrode in measurements of photochemical reaction rates.
Trans. Wisconsin Acad. Sci. 35: 221-233.
Manning, W. M., and Juday, Richard E. 1941. The chlorophyll content and
productivity of some lakes in northeastern Wisconsin. Ibid. 33: 363-394.
Manning, W. M., Juday, C., and Wolf, M. 1938. Photosynthesis in Chlorella.
Quantum efficiency and rate measurements in sunlight. Jour. Amer.
Chem. Soc. 60: 274-278. Notes and Reports No. 66.
- — 1938. Photosynthesis of aquatic plants at different depths
in Trout Lake, Wisconsin. Trans. Wisconsin Acad. Sci. 31: 377-410.
Marsh, C. D. 1891. Notes on the depth and temperature of Green Lake. Ibid.
8: 214-218.
— - 1891. On the deep-water Crustacea of Green Lake. Ibid.
8: 211-213.
- - - - — — 1892. On the Cyclopidae and Calanidae of central Wiscon¬
sin. Ibid. 9: 189-224.
- — - 1894. On the vertical distribution of pelagic Crustacea in
Green Lake, Wisconsin. Amer. Nat. 28: 807-809.
- - - 1895. On two new species of Diaptomus. Trans. Wisconsin
Acad. Sci. 10: 15-18.
- - — - 1898. On the limnetic Crustacea of Green Lake. Ibid. 11:
179-224.
- - - 1899. Hydrographic map of Green Lake. Wis. Geol. Survey,
Map No. 7.
— - ■ 1900. On some points in the structure of the larva of
Epischura lacustris Forbes. Trans. Wisconsin Acad. Sci. 12: 544-548.
— - - 1901. The plankton of freshwater lakes. (Address of the
retiring president.) Ibid. 13: 163-187.
- - 1903. The plankton of Lake Winnebago and Green Lake.
Wis. Geol. and Nat. Hist. Survey, Bull. 12, 94 pp.
_ _ _ 1907. A revision of North American species of Diaptomus.
Trans. Wisconsin Acad. Sci. 15: 381-516.
_ _ _ 1910. A revision of the North American species of Cyclops.
Ibid. 16: 1067-1134.
482 Wisconsin Academy of Sciences , Arts and Letters
- - - 1914. Structural abnormalities in Copepoda. Ibid. 17; 195-
196.
Marsh, Mrs. Florence W. (Mrs. C. D.) 1938. Professor C. Dwight Marsh and
his investigation of lakes. Ibid. 31; 535-543.
Marshall, Kuth. 1903. Ten species of Arrenuri belonging to the subgenus
Megalurus Thon. Ibid. 14: 145-172.
— - - - 1914. Some new American water mites. Ibid. 17: 1300-1304.
— - - - 1921. New American water mites of the genus Neumania.
Ibid. 20: 205-213.
— — — - - 1929. The morphology and developmental stages of a new
species of Piona. Ibid. 24: 401-404.
- 1930. The water mites of the Jordan Lake region. Ibid . 25:
245-253.
— - 1931-1940. Preliminary list of the Hydracarina of Wis¬
consin. Ibid. 26: 311-319. (1931) Part II. Ibid. 27: 339-357. (1932) Part
IH. Ibid. 28: 37-60. (1933) Part IV. Ibid. 29: 273-296. (1935) Part V.
Ibid. 30: 225-251. (1937) Part VI. Ibid. 32: 135-165. (1940).
Marshall, W. S. 1903. Entocythere cambari (nov. gen. et nov. sp.), a parasitic
ostracod. Ibid. 14: 117-144.
— - - 1913. The development of the wings of a caddisfiy, Platy-
phylax designatus Walk. Zeitsch. Wissenschaft. Zool. 105(4): 574-597.
- 1914. On the anatomy of the dragonfly, Libellula quadri-
maculata Linne. Trans. Wisconsin Acad. Sci. 17: 755-790.
Marshall, W. S., and Gilbert, N. C. 1905. Notes on the food and parasites of
some freshwater fishes from the lakes at Madison, Wisconsin. Report
U. S. Bureau of Fisheries, 1904: 513-522.
- 1905. Three new trematodes found principally in black
bass. Zoolog. Jahrb. Syst. 22: 477-488.
Marshall, W. S., and Severin, Henry. 1904. Some points in the anatomy of
Ranatra jusca P. Beauv. Trans. Wisconsin Acad. Sci. 14: 487-508.
Mavor, J. W., and Feinberg, S. M. 1918. Lymphocystis vitrei, a new sporozoan
from the pike-perch, Stizostediom vitreum Mitchill. Ibid. 19: 559-561.
Mavor, J. W., and Strasser, William. 1916. On a new myxosporidian, Hen -
neguya wisconsinensis, n. sp., from the urinary bladder of the yellow
perch, Perea fiavescens. Ibid. 18: 676-682.
- 1918. Studies of Myxosporidia from the urinary bladders
of Wisconsin fishes. Ibid. 19: 553-558.
Meloche, V. W., Leader, G., Safranski, L., and Juday, C. 1938. The silica and
diatom content of Lake Mendota water. Ibid. 31: 363-376.
Meloche, V. W., and Lohuis, Delmont. 1938. Sodium and potassium in lake
waters and lake water residues. Ibid. 31: 285-305.
Meloche, V. W., and Pingrey, Katherine. 1938. The estimation of magnesium
in lake water residues. Ibid. 31: 277-283.
Meloche, V. W., and Setterquist, T. 1933. The determination of calcium in
lake water and lake water residues. Ibid . 28: 291-296.
Merrill, Harriet Bell. 1893. The structure and affinities of Bunops scutifrom;
Birge. Ibid. 9: 319-342.
Miller, W. S. 1895. The anatomy of the heart of Cambarus. Ibid. 10: 327-33S.
Juday and Easier — Wisconsin Limnology Publications 483
Morrison, J. P. E. 1929. A preliminary list of the mollusca of Dane County,
Wisconsin. Ibid. 24: 405-425.
- - - - 1932. A report on the mollusca of the northeastern Wis¬
consin lake district. Ibid. 27: 359-396.
— — — - 1932. Studies on the life history of Acella haldemani
O’Desh.” Binney). Ibid. 27: 397-413.
Munro, Caroline Walker. 1921. A preliminary study of the digestive secre¬
tions of pickerel and perch. Ibid. 20: 269-273.
Muttkowski, R. A. 1918. The fauna of Lake Mendota. A qualitative and
quantitative survey with special reference to the insects. Ibid. 19: 374-
382.
Myers, F, J. 1930. The rotifer fauna of Wisconsin. V. The genera Euchlanis
and Monommata. Ibid. 25: 353-413.
Neidhofer, James R. 1938. Carteria tenosperma Potts, a species of freshwater
sponge new to Wisconsin. Trans. Amer. Micros. Soc. 57: 82-84.
— — - - - 1940. The freshwater sponges of Wisconsin. Trans. Wis¬
consin Acad. Sci. 32: 177-197.
Nelson, Merlin M., and Hasler, A. D. 1942. The growth, food, distribution and
relative abundance of the fishes of Lake Geneva, Wisconsin, in 1941,
Ibid. 34: 137-148.
Nelson, T. C. 1915. Raina palustris in Wisconsin. Copeia 19: 13-14.
Noland, L. E. 1925. Factors influencing the distribution of freshwater ciliates.
Ecology 6: 437-452.
- — - - - 1925. A review of the genus Coleps with descriptions of
two new species. Trans. Amer. Micros. Soc. 44: 3-12.
Noland, L. E., and Finley, H. E. 1931. Studies on the taxonomy of the genus
Vorticella. Ibid. 50: 81-123.
O’Donnell, D. John. 1942. The fish population in three small lakes in north¬
ern Wisconsin. Trans. Amer. Fisheries Soc. 72: 187-196.
Olive, Edgar W. 1905. Notes on the occurrence of Oscillatoria prolifica (Gre-
ville) Gomont in the ice of Pine Lake, Waukesha County, Wisconsin.
Trans. Wisconsin Acad. Sci. 15: 124-134.
Pearse, A. S. 1915. On the food of the small shore fishes in the waters near
Madison, Wisconsin. Bull. Wis. Nat. Hist. Soc. 13: 7-22.
- 1918. Food of the shore fishes of certain Wisconsin lakes.
Bull. U. S. Bureau Fisheries 35: 245-292.
- - — 1919. Habits of the black crappie in inland lakes of Wis¬
consin. Rept. U. S. Com. Fish, for 1918. Appendix 3: 5-16.
— - — 1921. Distribution and food of the fishes of Green Lake,
Wisconsin, in summer. Bull. U. S. Bureau Fisheries 37: 253-272.
- 1921. Distribution and food of the fishes of three Wiscon¬
sin lakes in summer. Univ. of Wisconsin Studies No. 17.
— - 1921. Habits of the mudpuppy Necturus, an enemy of food
fishes. Bur. Fish Economic Circ. No. 49, 8 pp.
— - 1923. The abundance and migration of turtles. Ecology 4:
24-28.
— - - — - 1923. The growth of the painted turtle. Biol. Bull. 45:
145-148.
484 Wisconsin Academy of Sciences , Arts and Letters
- 1924. Amount of food eaten by four species of freshwater
fishes. Ecology 5: 254-258.
- 1924. Observations on parasitic worms from Wisconsin
fishes. Trans. Wisconsin Acad. Sci. 21: 147-160.
- 1924. The parasites of lake fishes. Ibid. 21: 161-194.
- 1925. Chemical composition of certain freshwater fishes.
Ecology 6: 7-16.
- 1934. Ecology of lake fishes. Ecol. Monog. 4: 475-480.
Pearse, A. S., and Achtenberg, Henrietta. 1920. Habits of yellow perch in
Wisconsin lakes. Bull. U. S. Bureau Fisheries 36: 293-366.
Pennak, R. W. 1939. The microscopic fauna of the sandy beaches. In Prob¬
lems in Lake Biology. Published by Amer. Assoc. Adv. Sci. Pub. No. 10:
94-106.
- 1940. Ecology of the microscopic metazoa inhabiting the
sandy beaches of some Wisconsin lakes. Ecol. Monog. 10: 537-615.
Peterson, W. H., Fred E. B., and Domogalla, B. P. 1925. The occurrence of
amino acids and other organic nitrogen compounds in lake waters. Jour.
Biol. Chem. 63: 287-295.
Pietenpol, W. B. 1918. Selective absorption in the visible spectrum of Wis*
consin lake waters. Trans. Wisconsin Acad. Sci. 19: 562-593.
Pope, T. E. B. 1938. Landlocked salmon in Wisconsin. Ibid. 31: 559-567.
Pope, T. E. B., and Dickinson, W. E. 1928. The amphibians and reptiles of
Wisconsin. Public Museum of the City of Milwaukee. Bull. 8: 1-138.
Potzger, John E. 1942. Pollen spectra from four bogs on the Gillen Nature
Reserve, along the Michigan- Wisconsin state line. Amer. Midland Nat.
28: 501-511.
- 1943. Pollen analysis of five bogs in Sawyer and Price
Counties, Wisconsin. Butler Univ. Bot. Studies 6: 54-64.
Potzger, John E., and Keller, C. O. 1942. A pollen study of four bogs along
the southern border of Vilas County, Wisconsin. Trans. Wisconsin Acad.
Sci. 34: 149-166.
Potzger, John E., and Richards, Ruth R. 1942. Forest succession in the Trout
Lake, Vilas County, Wisconsin area: a pollen study. Butler Univ. Bot.
Studies 5: 179-189.
Potzger, John E., and Van Engel, Willard A. 1943. Study of the rooted aquatic
vegetation of Weber Lake, Vilas County, Wisconsin. Trans. Wisconsin
Acad. Sci. 34: 149-166.
Rickett, H. W. 1921. A quantitative study of the larger aquatic plants of
Lake Mendota. Ibid. 20: 501-527.
- 1924. A quantitative study of the larger aquatic plants of
Green Lake, Wisconsin. Ibid. 21: 381-414.
Robinson, Rex J., and Kemmerer, C. I. 1930. The determination of Kjeldahl
nitrogen in natural waters. Ibid. 25: 123-128.
— - 1930. Determination of organic phosphorus in lake waters.
Ibid. 25: 117-121.
- - 1930. Determination of silica mineral waters. Ibid. 25: 129-
134.
Rodgers, Nelson E., and McCoy, Elizabeth. 1942. Some aspects of the micro¬
biology of the beach sands of freshwater lakes. Ms.
Juday and Hosier — Wisconsin Limnology Publications 485
Schloemer, Clarence L. 1936. The growth of the muskellunge Esox masqui-
nongy immaculatus (Garrard) in various lakes and drainage areas of
northern Wisconsin. Copeia 1936: 185-193.
— - - - 1938. A second report on the growth of the muskellunge
Esox masquinongy immaculatus (Garrard) in Wisconsin waters. Trans.
Wisconsin Acad. Sci. 31: 507-512.
- - - - 1939. The age and rate of growth of the bluegill, Helio-
perca macrochira (Rafinesque) . Manuscript Ph.D. Thesis. 113 pp. Li¬
brary, Univ. of Wisconsin.
Schloemer, Clarence L., and Lorch, Ralph. 1942. The rate of growth of the
wall-eyed pike, Stizostedion vitreum (Mitchill), in Wisconsin’s inland
waters, with special reference to the growth characteristics of the Trout
Lake population. Copeia 1942: 201-211.
Schnabel, Zoe Emily (Mrs. G. E. Albert) . 1938. Estimation of total fish popu¬
lation of a lake. Amer. Math. Monthly 45: 348-352.
Schneberger, E. 1931. How old was that big fish you caught up in northern
Wisconsin this summer? Wisconsin Magazine. July-August 1931: 3-4 and
22-23.
- 1933. Scales tell age of fishes, Wisconsin survey reveals.
Our Own Out-of-Doors 2: 4-5 and 13-15. June.
- — - 1935. Growth of the yellow perch in Nebish, Silver and
Weber Lakes. Trans. Wisconsin Acad. Sci. 29: 103-130.
- - 1936. The biological and economic importance of the smelt
in Green Bay. Trans. Amer. Fisheries Soc. 66: 139-142.
- — - — — 1937. Natural production of muskellunge. Wis. Cons. Dept.
Report. 17 pp. Mimeographed.
- 1939. Does ice fishing aerate the water? Wis. Cons. Bull. 4:
33-35.
Schneberger, Edw., and Hasler, A. D. 1944. Brule River survey: Introduction.
Trans. Wisconsin Acad. Sci. 36 (in press).
Scheme r, Harold A. 1934. Photosynthesis of water plants at various depths
in the lakes of northeastern Wisconsin. Ecology 15: 217-218.
Schomer, H. A., and Juday, C. 1935. Photosynthesis of algae at different
depths in some lakes of northeastern Wisconsin. I. Observations in 1933
Trans. Wisconsin Acad. Sci. 29: 173-193.
Schuette, H. A. 1918. A biochemical study of the plankton of Lake Mendota.
Ibid. 19: 594-613.
Schuette, H. A., and Alder, H. 1927. Notes on the chemical composition of
some of the larger aquatic plants of Lake Mendota. Vallisneria and
Potamogeton. Ibid. 23: 249-254.
- - - 1929. A note on the chemical composition of Chara from
Green Lake, Wisconsin. Ibid. 24: 141-145.
- - - 1929. Notes on the chemical composition of some of the
larger aquatic plants of Lake Mendota. HI. Castalia odorata and Najas
flexilis. Ibid. 24: 135-139.
Schuette, H. A., and Hoffman, Alice. 1922. Notes on the chemical composition
of some of the larger aquatic plants of Lake Mendota. I. Cladophora and
Myriophyllum. Ibid. 20: 529-531.
486 Wisconsin Academy of Sciences, Arts and Letters
Shelford, V. E., and Kunz, J. 1926. The use of photoelectric cells of different
alkali metals and color screens in the measurement of light penetration
into water. Ibid. 22: 283-298.
Smith, B- C. 1911. The nests and larvae of Necturus. Biol. Bull. 20: 191-200,
Smith, C. M. 1913. Tetradesmus, a new four-celled coenobic alga. Torrey
Botan. Club 40: 75-87.
— - — — - 1914. The organization of the colony in certain four-celled
coenobic algae. Trans. Wisconsin Acad. Sci. 17: 1165-1220.
- — - 1916. A monograph of the algal genus Scenedesmus based
upon pure culture studies. Ibid. 18: 422-530.
- — - 1916. New or interesting algae from the lakes of Wisconsin.
Torrey Botan. Club 43: 471-483.
— - - 1916. A preliminary list of algae found in Wisconsin lakes.
Trans. Wisconsin Acad. Sci. 18: 531-565.
- 1917. The vertical distribution of Volvox in the plankton
of Lake Monona. Amer. Jour. Bot. 5: 178-185.
— — - 1918. A second list of algae found in Wisconsin lakes.
Trans. Wisconsin Acad. Sci. 19: 614-654.
- 1920. Phytoplankton of the inland lakes of Wisconsin.
Part I. Myxophyceae, Phaeophyceae, Heteronkonteae, and Chlorophyceae
exclusive of the Desmidiaceae. Bull. No. 57, Wis. Geol. and Nat. Hist.
Survey. 243 pp. 51 pis.
- 1924. Phytoplankton of the inland lakes of Wisconsin.
Part II. Desmidiaceae. Bull. Part II. Wis. Geol. and Nat. Hist. Survey.
227 pp. Pis. 52-88. Also Bull. No. 1270, Univ. of Wisconsin.
Smith, Winslow Whitney. 1940. Production of anti-bacterial agglutinins by
carp and trout at 10° C. Proc. Soc. Exptl. Biol. Med. 45: 726-729.
Snow, Letitia M., and Fred, E. B. 1926. Some characteristics of the bacteria
of Lake Mendota. Trans. Wisconsin Acad. Sci. 22: 143-154.
Spoor, W. A. 1935. On the sexual dimorphism of Catostomus commersonii .
Copeia 1935: 167-171.
- 1938. Age and growth of the sucker, Catostomus commer¬
sonii (Lacepede), in Muskellunge Lake, Vilas County, Wisconsin. Trans.
Wisconsin Acad. Sci. 31: 457-505.
Spoor, William A., and Schloemer, C. L. 1939. Diurnal activity of the common
sucker, Catostomus commersonii , and rock bass, Ambloplites rupestris, in
Muskellunge Lake. Trans. Amer. Fisheries Soc. 68: 211-220.
Stadler, Janice, and ZoBell, C. E. 1939. Evidence of the aerobic decomposition
of lignin by lake bacteria. Jour. Bact. 38: 115. Abstract.
Stark, W. H., and McCoy, Elizabeth. 1938. Distribution of bacteria in certain
lakes of northern Wisconsin. Centralbl. f. Bakt., Parasitenk. u. Infektion-
skrank. 98: 201-209.
Steiner, John, and Meloche, V. 1935. A study of ligneous substances in
lacustrine materials. Trans. Wisconsin Acad. Sci. 29: 389-402.
Symposium on Hydrobiology. 1941. Published by University of Wisconsin
Press. Contains papers relating to various fields of hydrobiology. 405 pp.
Taylor, F. H. L. 1928. A complete systematical analysis of lake water residues
Juday and Hosier — Wisconsin Limnology Publications 487
by a new micro method. Unpublished thesis. 1928. 57 pp. Library, Univ.
of Wisconsin.
Thomson, John W., Jr. 1940. Preliminary reports on the flora of Wisconsin.
XXVII. Lentibulariaceae. Trans. Wisconsin Acad. Sci. 32: 85-89.
Thwaites, F. T. 1929. Glacial geology of part of Vilas County, Wisconsin.
Ibid. 24: 109-125.
Titus, Leslie, and Meloche, V. W. 1931. Note on the determination o£ total
phosphorus in lake water residues. Ibid. 26: 441-444.
- - - - — 1933. A microextractor. Indus, and Eng. Chem. 5: 286-291.
Trelease, William. 1889. The “working” of Madison lakes. Trans. Wisconsin
Acad. Sci. 7: 121-129.
Tressler, W. L., and Domogalla, B. P. 1931. Limnological studies of Lake
Wingra. Ibid. 26: 331-351.
Turner, C. L. 1919. The seasonal cycle in the spermary of the perch. Jour.
Morphol. 32: 681-705.
Twenhofel, W. H. 1933. The physical and chemical characteristics of the
sediments of Lake Mendota, a freshwater lake of Wisconsin. Jour. Bedim.
Petrol. 3: 68-76.
- — — — — - 1937. The bottom sediments of Lake Monona, a freshwater
lake of southern Wisconsin. Ibid. 7: 67-77.
Twenhofel, W. H., and Broughton, W. A. 1939. The sediments of Crystal
Lake, an oligo trophic lake in Vilas County, Wisconsin. Amer. Jour. Sci.
237: 231-252.
Twenhofel, W. H., Carter, S. L., and McKelvey, V. E. 1942. The sediments
of Grassy Lake, Vilas County, a large bog lake of northern Wisconsin.
Ibid. 240: 529-546.
Twenhofel, W. H., and McKelvey, V. E. 1939. Sediments of Devils Lake,
a eutrophic-oligotrophic lake of southern Wisconsin. Jour. Sedim. Petrol.
9(3): 105-121. December.
— — - - 1941. The sediments of freshwater lakes. Bull. Amer. Assoc.
Petrol. Geol. 25: 826-849.
- - — 1942. The sediments of Little Long (Hiawatha) Lake, Wis¬
consin. Jour. Sedim. Petrol. 12:36-50.
Twenhofel, W. H., McKelvey, V. E., Carter, S. A., and Nelson, Henry. 1944.
The sediments of four woodland lakes, Vilas County, Wisconsin. Parts I
and II. Amer. Jour. Sci. 242: 19-44.
Van Engel, W. A. 1940. The rate of growth of the northern pike, Esox Indus
Lin., in Wisconsin waters. Copeia 1940: 177-187.
Vorhies, C. T. 1905. Habits and anatomy of the larva of the caddisfly, Platy -
phylax designatus, Walker. Trans. Wisconsin Acad. Sci. 15: 108-123.
- - — 1909. Studies on the Trichoptera of Wisconsin. Ibid. 16:
647-738.
Wagner, George. 1904. Notes on Polyodon I. Science, N.S. 19: 554-555.
— - - 1908. The tullibee ( Argyrosomus tullibee Richardson) as a
fish of economic importance. Bienn. Rept. Com. of Fisheries Wis. 1907/08,
pp. 152-155.
488 Wisconsin Academy of Sciences , Arts and Letters
- 1909. Notes on the fish fauna of Lake Pepin. Trans. Wis¬
consin Acad. Sci. 16: 23-37.
— - 1910. Argyrosomus johannae, a new species of Cisco from
Lake Michigan. Science, N.S. 31: 957-958.
- - 1910. On the stickleback of Lake Superior. Ibid. 32: 28-30.
- 1911. The cisco of Green Lake, Wisconsin. Bull. Wis. Nat.
Hist. Soc. 9: 73-77.
Wagner, George, and Juday, C. 1908. Dissolved oxygen as a factor in the dis¬
tribution of fishes. Trans. Wisconsin Acad. Sci. 16: 17-22.
Whitney, L. V. 1937. Microstratification of the waters of inland lakes in
summer. Science, N.S. 85: 224-225. Feb. 26.
• - 1938. Microstratification of inland lakes. Trans. Wisconsin
Acad. Sci. 31: 155-173.
- 1938a. Continuous solar radiation measurements in Wis¬
consin lakes. Ibid. 31: 175-200.
- 1938b. Transmission of solar energy and the scattering pro¬
duced by suspensoids in lake waters. Ibid. 31: 201-221.
- 1941. A multiple electromagnetic water sampler. Ibid. 33:
95-97.
- 1941a. The general law of diminution of light intensity and
the per cent of diffuse light at different depths in lake waters. Jour.
Optic. Soc. Amer. (In press.)
- 1941b. The angular distribution of characteristic diffuse
light in natural waters. Jour. Mar. Res. 4: 122-131.
Williams, F. T., and McCoy, Elizabeth. 1934. The role of microorganisms in
the precipitation of calcium carbonate in the deposits of freshwater lakes.
Jour. Sedim. Petrol. 4: 113-126.
- 1935. The microflora of the mud deposits of Lake Mendota
Ibid. 5: 31-36.
Williamson, Lyman O., and Schneberger, Edward. 1942. The results of plant¬
ing legal-sized trout in the Deerskin River, Vilas County, Wisconsin.
Trans. Amer. Fisheries Soc. 72: 92-96.
Wilson, L. R. 1935. Lake development and plant succession in Vilas County,
Wisconsin. Part I. The medium hard water lakes. Ecol. Monog. 5: 207-
247.
_ _ 1937. A quantitative and ecological study of the larger
aquatic plants of Sweeney Lake, Oneida County, Wisconsin. Bull. Torrey
Botan. Club 64: 199-208.
- - - 1938. The postglacial history of vegetation in northern Wis¬
consin. Rhodora 40: 137-175. April.
_ _ 1939. Rooted aquatic plants and their relation to the lim¬
nology of freshwater lakes. Problems in lake biology. Publ. by Amer.
Assoc. Adv. Sci. Pub. No. 10: 107-122.
_ _ _ — 1939. A temperature study of a Wisconsin peat bog. Ecol¬
ogy 20: 432-433. July.
_ _ 1941. The larger aquatic vegetation of Trout Lake, Vilas
County, Wisconsin. Trans. Wisconsin Acad. Sci. 33: 135-146.
Wilson, L. R., and Cross, A. T. 1941. A study of the microfossil succession in
Juday and Hasler — Wisconsin Limnology Publications 489
the bottom deposits of Crystal Lake, Vilas County, Wisconsin, and the
peat of a nearby bog. (In press.)
Wilson, L. R., and Galloway, E. F. 1937. Microfossil succession in a bog in
northern Wisconsin. Ecology 18: 113-118.
Wilson, L. R., and Webster, R. M. 1942. Fossil evidence of a wider postglacial
range of hickory and butternut in Wisconsin. Rhodora 44: 409-414.
- - - - - 1942. Microfossil studies of three north central Wisconsin
bogs. Trans. Wisconsin Acad. Sci. 34: 177-193.
Wimmer, E. J. 1929. A study of two limestone quarry pools. Ibid. 24: 363-399.
Woltereck, R. 1932. Races, associations and stratification of pelagic daphnids
in some lakes of Wisconsin and other regions of the United States and
Canada. Ibid. 27: 487-520.
Woodbury, Lowell A. 1941. A sudden mortality of fishes accompanying a
supersaturation of oxygen in Lake Waubesa, Wisconsin. Trans. Amer.
Fisheries Soc. 71: 112-117.
- - — — 1942. Vitamin Bi deficiency in hatchery reared rainbow
trout. Ibid. 72: 30-34.
Wright, Stillman. 1929. A preliminary report on the growth of the rock bass,
Ambloplites rupestris (Rafinesque), in two lakes of northern Wisconsin.
Trans. Wisconsin Acad. Sci. 24: 581-595. Figs.
ZoBell, C. E. 1940. Some factors which influence oxygen consumption by
bacteria in lake water. Biol. Bull. 78: 388-402.
ZoBell, C. E., and Stadler, Janice. 1940a. The effect of oxygen tension on the
oxygen uptake of lake bacteria. Jour. Bact. 39: 307-322.
— - - 1940b. The oxidation of lignin by lake bacteria. Arch. f.
Hydrobiol. 37: 163-171.
Addenda
Bangham, Ralph V. 1944. Parasites of northern Wisconsin fish. Trans. Wis¬
consin Acad. Sci. 36: (In press).
Birge, Edward A. 1945. The effect of dissolved color on the vertical trans¬
mission of light in filtrates of lake waters. Trans. Wisconsin Acad. Sci.
36: (In press).
Cole, Arch E. 1921. Oxygen supply of certain animals living in water con¬
taining no dissolved oxygen. Jour. Exptl. Zool. 33(1): 293-320.
Colmer, Arthur Russell, and McCoy, Elizabeth. The genus Micromonospora
in relation to some Wisconsin lakes. Trans. Wisconsin Acad. Sci. 35: 187-
220.
Held, John B., Herman, Elmer F., Elvehjem, C. A., and Schneberger, Edward.
1944. Note on a controlled feeding technique in nutrition studies in trout.
Copeia: (In press.)
Jansky, Mary A. 1936. The characterization of some bacteria from northern
Wisconsin lakes with emphasis on the chromogens. Ms. M.S. Thesis.
32 pp. Library, University of Wisconsin.
Kinkel, Dorothy E. 1936. A study of chitin-, pectin-, and cellulose -destroying
bacteria from lake mud. Ms. M.S. Thesis. 34 pp. Library, University of
Wisconsin.
490 Wisconsin Academy of Sciences , Arts and Letters
Prescott* G. W. 1944. New species and varieties of Wisconsin algae. Farlowia.
1(3): 349-385.
Schneberger, Edward, and Woodbury, Lowell A. 1944. The lake sturgeon,
Acipenser fulvescens Rafinesque, in Lake Winnebago, Wisconsin. Creel
census, age, length, and weight. Trans. Wisconsin Acad. Sci. 36: (In
press) .
Stark, William H. 1939. Part I. Factors influencing the bacterial populations
of freshwater lakes. Ms. Ph.D. Thesis. 18 pp. Library, University of
Wisconsin.
tors. II. Centers of activity in lakes. Ms. M.S. Thesis. 62 pp. Library,
Stark, William H. 1937. Growth of freshwater bacteria. I. Controlling fac-
University of Wisconsin.
Wolf, F. T. 1944. The aquatic oomycetes of Wisconsin. Part I. Univ. Wig.
Press. 64 pp.
PROCEEDINGS OF THE ACADEMY
Seventy-Fourth Annual Meeting
The seventy-fourth annual meeting of the Academy was held in Memorial
Union at the University of Wisconsin, Madison, Wisconsin, on Friday and
Saturday, April 14 and 15, 1944. Three other organizations participated jointly
in the meeting, — the Wisconsin Archeological Society, Wisconsin Museums
Conference, and the Wisconsin Folklore Society. The Academy section met in
Room 119, Science Hall, while the other sections held meetings in the Recep¬
tion Room, University Memorial Union. Approximately 100 persons attended
the various meetings. The annual business meeting and election of officers
was held on Friday afternoon. The following program of papers was presented.
Archeological, Folklore, and Museums Section
Friday morning
Esther Hemingway, Madison, Museum Exhibits; Nancy Oestreich, Mil¬
waukee, Wampum; G. Wm. Longenecker, Madison, The University of Wis¬
consin Arboretum; Edna McChesney Bullard, Madison, The Powder Room at
Eden Dale; George Urdang, Madison, The Story of Cinchona; Vivien J. Dube,
Superior, Early Water Craft of the Head of the Lakes; Dorothy Moulding
Brown, Madison, Americana; P. E. McNall, Madison, Tall Tales of Kansas;
J. F. Wojta, Madison, German Household Admonitions; L. P. Jerrard, Win-
netka, Illinois, Three Marquette County Indian Mound Groups; Jean Gordon
Smith, Madison, Nature Study at the Wisconsin Orthopedic Hospital; Mrs.
Peter Diedrich, Lake Mills, Activities of the Lake Mills-Aztalan Historical
Society; Olive Jacobs, Hudson, St. Croix River Legends; Victor S. Taylor,
Lake Mills, Graveyard Tales from the Jefferson County area.
Academy Section
Friday afternoon
H. P. Thomsen, University of Wisconsin (Introduced by Arthur D. Hasler) ,
Territories of the Red Winged Blackbird of the University Bay Region;
Elizabeth Jones, University of Wisconsin (Introduced by Arthur D. Hasler),
Aquatic Plants in Winter; Benson H. Paul, Forest Products Laboratory (Intro¬
duced by Arthur Koehler) , Second Growth May Supply Timber of Exceptional _
Quality; H. P. Thomsen, University of Wisconsin, The Social Behavior of the
Whitefooted Mouse in Winter; Aldo Leopold, Ernest F. Bean, and Norman C.
Fassett, University of Wisconsin, Report of the Conservation Committee of the
Academy; Michael F. Guyer, University of Wisconsin, Memorial to Chancey
491
492 Wisconsin Academy of Sciences , Arts and Letters
Juday, Past President and Life Member of the Academy; Clayton S. Moses,
Forest Products Laboratory (Introduced by C. Audrey Richards), Oak Wilt in
Wisconsin; Eric Miller, University of Wisconsin, Snow Cover in Wisconsin;
Ruth Marshall, Wisconsin Dells, Wisconsin, A Revision of Part I, Preliminary
List of the Hydracarina of Wisconsin (By Title) .
Archeological, Folklore, and Museums Section
Friday afternoon
Zida C. Ivey, Fort Atkinson, The Preservation of the Hoard Mounds;
Dorothy J. Kundert, Monroe, Green County Folktales; Harvey Leaman,
Neenah, The Grand Loggery; J. S. Slotkin, Madison, The Earliest Racial
Classifications of the 17th and 18th Centuries; Allie Freeman, Horicon, Dodge
County Territorial Post Offices; Helene Stratman-Thomas, Madison, Kentucky
Folksongs in Wisconsin; Mrs. Merton Smith, Beloit, The Beloit Historical
Museum; Mrs. Ethel Stauffacher, New Glarus, The New Glarus Museum
Project; W. C. English, Wyocena, Wisconsin Cave Museums; George Overton,
Butte des Morts, The Poygan Playground; Herbert W. Kuhm, Milwaukee,
Indian Decorative Uses of Shell.
Academy Section
Saturday morning
Edward A. Birge, University of Wisconsin, Changes in the Transmission
of Light Through Filtered Lake Waters, Produced by the Presence of Dissolved
Color Material; C. L. Fluke, University of Wisconsin and F. M. Hull, Univer¬
sity of Wisconsin, A Review of the Syrphid Flies of the Genus Cheilosia, sub-
genus Chilomyia; Banner Bill Morgan, University of Wisconsin, Bovine Trich¬
omoniasis in Wisconsin; Frederick L. Browne, Forest Products Laboratory,
When and Why We Paint Houses; Elizabeth McCoy and Wayne W. Umbreit,
University of Wisconsin, The Bacteriological Problems in the Retting of Hemp;
Kenneth P. Buchholtz, University of Wisconsin (Introduced by R. J. Mucken-
hirn), Agronomic and Breeding Investigations on Hemp; Harland W. Moss-
man, University of Wisconsin, Observations on the Breeding of Wisconsin
Squirrels; John P. Limbach, Forest Products Laboratory (Introduced by
Louise Gerry) , An Inexpensive Exposure Meter for Photomicrography (Dem¬
onstration) ; H. A. Schuette and F. J. Schubert, University of Wisconsin,
Hydrogen Ion Concentration of Honey; Arthur D. Hasler, University of Wis¬
consin, Depth Distribution in Winter of the Perch in Lake Mendota; Myles
Dillon, University of Wisconsin, Italic and Celtic; Carroll V. Sweet, Forest
Products Laboratory, Gasogens; Dr. W. D. Stovall, University of Wisconsin,
Blood Groups and Hemolytic Reactions Following Blood Transfusions; K. C.
Berger and E. Truog, University of Wisconsin, Boron Deficiency in Beets as
Revealed by Yields and Soil Tests; H. C. Greene, University of Wisconsin,
Fungi of the University of Wisconsin Arboretum; R. I. Evans, University of
Wisconsin, L. S. Cheney’s “Mosses of Wisconsin” (By Title).
Proceedings of the Academy
493
Archeological, Folklore, and Museums Section
Saturday morning
Ella Stratton Colbo, Racine, Harriet Stewart Hartington, Civil War Nurse;
Frederic G. Cassidy, Madison, The Names of the Madison Four Lakes; Earl
Seidlinger, Columbus, The Florida Mosquitos, Service Tall Tales; Albert O.
Barton, Madison, A Pioneer Scotch Cooperative in Dane County; Ted Mueller,
Milwaukee, Some Old Milwaukee Folktales; J. Stanley Dietz, Madison, Civil
War Songs; Charles E. Brown, Madison, Wisconsin Indian Trailside Shrines;
Louis A. Maier, Milwaukee, Mystic Knights of the Blue Ox; Warren Wittry,
Robert Linck and Robert Hall, Green Bay, Discovery of an Indian Rockshelter
in Brown County.
Annual Academy Lecture
The annual Academy dinner was held on Friday evening, April 14, in
Room 119, Science Hall. Two addresses were made. President A. W. Schorger
of Madison presented his presidential talk, the title of which was “The Abun¬
dant Life.” Professor Leon J. Cole of the University gave an illustrated talk
on “Life of the Fur Seals of the Pribilof Islands.”
Academy Business Meeting
The annual business meeting was held in Science Hall on Friday after¬
noon, April 14, 1944.
Committee on nominations: R. J. Muckenhirn, E. F. Bean, Philo Buck, Jr.
and H. W. Mossman presents the following slate of officers for the next Acad¬
emy year:
President: H. A. Schuette, University of Wisconsin, Madison.
Vice Presidents:
In Science — Ruth Walker, Milwaukee.
In Arts — Walter Bubbert, Milwaukee
In Letters — Helen White, University of Wisconsin, Madison.
Secretary-Treasurer: Banner Bill Morgan, University of Wisconsin, Madison.
Librarian: Halvor O. Teisberg, State Historical Society, Madison.
Curator: Edward P. Alexander, State Historical Society, Madison.
494 Wisconsin Academy of Sciences , Arts and Letters
Treasurer's Report
April 12, 1944
Receipts
Carried forward in Treasury, April 20, 1943 . . . .$2,462,011
Receipts from dues, April 20, 1943-April 12, 1944 . . 651,23
Final distribution by Trustees for liquidation of Chapman
Building Company Certificates owned by Academy . . 382.20
Sale of publications . . . . . 219.76
Sale of reprints to authors . . . . . 180.57
Interest on endowment . 89.00
Grant-in-Aid for research from A.AA.S. . . . 81.50
Extra printing costs paid by authors . 34.75
Total receipts . $4,101.02
Disbursements
Purchase of U. S. Savings Bonds, Series G . .$1,600.00
Deposit on expenses for cuts for Vol. 35 . . . 100.00
Allowance to Secretary-Treasurer Loyal Durand for last one-half
of 1942-43 Academy year . . . 100.00
During the Academy year, 1936-1937, only $100 of his $200
annual allowance was withdrawn by the Secretary-Treas¬
urer. Payment of the remaining $100 was deferred each year
thereafter; such deferment is discontinued in the present
year with the result that a total of $300 rather than the
$200 provided for in the By-Laws is paid as Secretary-
Treasurer’s allowance for the 1943-1944 Academy year.
Allowance to Secretary-Treasurer ( 3A to Loyal Durand, lA to
R. J. Muckenhirn) for 1943-44 Academy year . . . . 200.00
Grant-in-Aid for research to Harold C. Hanson . 81.5©
Stamps, envelopes, and express charges . 32.02
Printing programs for 1943 and 1944 meetings . . . 35.75
Ledger sheets, rubber stamp, and record book . 3.85
Rental, safe deposit box . . . 3.6©
Total disbursements . . . $2,156.72
Balance, April 12, 1944, $1,944.30.
A check for $2.00 received from a Canadian bank is not
credited by the bank as of April 12, 1944, pending collection
and determination of discount and exchange charges.
R. J. Muckenhirn
Acting Secretary-Treasurer
Banner Bill Morgan
Secre tar y -Treasurer
Proceedings of the Academy
495
Endowments and Assets of the Wisconsin Academy of
Sciences, Arts and Letters
March 17, 1944
1. Home Owners Loan Coupon Bond Series A — AM383877H . $1,000.00
2. Home Owners Loan Coupon Bond Series A — AR1G3687H . 50.00
3- U.S. Treasury-Coupon Bond 1692B . 1,000.00
4. U.S. Treasury-Coupon Bond 12894D . . . 500.00
5. U.S. Savings Bond Registered Series G-M1696059G . . 1,000.00
6. U.S. Savings Bond Registered Series G-C1563347G . 100.00
7. U.S. Savings Bond Registered Series G-C1563348G . 100.00
Total Amount of Endowment . 3,750.00
8. UJS. Savings Bond Registered Series G-2386504G . 100.00
9. U.S. Savings Bond Registered Series G-2386505G . 100.00
10. U.S. Savings Bond Registered Series G-2386506G . 100.00
11. U.S. Savings Bond Registered Series G-2386507G . 100.00
Current Assets of Academy Invested in U.S. Bonds . 400.00
Total . . . . .$4,150.00
'The auditing committee has examined the accounts of the Treasurer and
the contents of the safe deposit box belonging to the Academy and has found
fchem in order.
H. A. Schuexte (signed)
Raymond J. Roark (signed)
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