WAS
8332
Volume 103
Number 3
Fall 2017
Journal of the
WASHINGTON Rat eel
NOV 27 2017
HARVARD
UNIVERSITY
ACADEMY OF SCIENCES
MeN CS CORAM NESE ES OUY Ieee aoe ecco veces che vc ccectincdevcb in cducvasccseicccescubedecoecencbviasodesssaevssonsees ii
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Description of a New Species of Cestode Parasitic Worm S. Banerjee et dl. ............. 17
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Washington Academy of Sciences
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Volume 103
Number 3
Fall 2017
Journal of the
WASHINGTON
ACADEMY OF SCIENCES
Editor's Comments S. Howard
Rae ENOS E EOES ERED MEAL CLIN OS ses sede pers ss east ics es die at wiaasdeed oe nines aR ili
How Wet Do You Get In The Raitt 7) LIDSCOMD: ...cccccccc.cscccesseessvesivescsossonnsessassacganssassovnursassannonrese 1
Description of a New Species of Cestode Parasitic Worm S. Banerjee et ai. ............. 17
ities elity op/at fol) [ci] dbo; eaee aes eee ian at ae enee feet Meare ON reek e deere ts amr epee See 29
Wa Mes UEC TCHIN, CCN, MEER ONS 20352205 oe S020 0os cel. Staak Oe Meets fasta ce RE x em Lee 30
PRE RR AES CA VEL UNUM AES 2 aay cise oo cer cect cae dav as A waa T ees area
ISSN 0043-0439 Issued Quarterly at Washington DC
Fall 2017
EDITOR’S COMMENTS
Herein is the 2017 Fall issue of the Journal. This is an exciting time for
science. Studies of the brain are providing new insights into human
behavior. Recently the Laser Interferometer Gravitational Wave
Observatory (LIGO) has measured black hole collisions. I hope that our
readers will contribute papers on these topics.
For this issue we have two quite different papers. One is an
interesting study on raindrops. Have you ever wondered how wet you get
when running in the rain? The other reports on the discovery of a new genus.
It comes from colleagues in India. This 1s their second report of a discovery
in our Journal.
Letters to the editor are encouraged. Please send email
(wasjournal@washacadsci.org) comments on papers, suggestions for
articles, and ideas for what you would like to see in the Journal. We are a
peer reviewed journal and need volunteer reviewers. If you would like to be
on our reviewer list please send email to the above address and include your
specialty.
The sciences remain at the forefront of human progress. This
Journal contributes to that effort. Without an extensive variation in what we
study we step backward. One never can tell what useful result will come
from an otherwise rare study. I offer one example. Many years ago there
was a scientist who studied slugs found on the Massachusetts shoreline. His
interest was only the slugs. The fact that slugs seemed to have a method of
controlling bleeding was a side interest. When this odd result was
discovered by medical researchers they found a solution to a long standing
medical problem: hemophilia. Such a result cannot be predicted. Science
must wander where it will. Out of those wanderings come solutions to today
and tomorrows’ problems.
Sethanne Howard
Washington Academy of Sciences
il
Journal of the Washington Academy of Sciences
Editor Sethanne Howard showard@washacadsc1.org
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Sciences Terrell Erickson terrell.erickson] @wdc.nsda.gov
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Science Education Jim Egenrieder jim@deepwater.org
Systems Science Elizabeth Corona elizabethcorona@gmail.com
Fall 2017
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HOW WET DO YOU GET IN THE RAIN, IF YOU DON’T
CARE HOW WET YOU GET?
Water absorption by walkers and runners indifferent
to precipitation
T.C, Lipscombe
Catholic University of America
Abstract
Many researchers have discussed the optimum speed at which to walk in
the rain to get the least wet. This article looks at a related problem: if
walkers or runners are indifferent to the rain, how drenched do they become
during their journeys home? The semi-empirical answer employs basic
introductory physics and biomechanics, as well as anthropometric
formulas related to human-body ratios.
Introduction
A VENERABLE PROBLEM in applied mathematics and physics is to answer
the question “How fast should you walk in the rain to get the least wet?”
Many articles address this subject — and variations thereof — for a variety
of audiences. Early papers were aimed mostly at a mathematical
audience.!»*»? The typical result is that if the rain is at the walker’s back,
then the walker’s optimal speed equals the rain speed. In any other situation,
the walker should go as fast as possible.* Others explored related topics.
The pseudonymous Hailman and Torrents looked at the effect of ellipsoidal
walkers? while Banks allowed for splashing from the sidewalk.® As befits
meteorologists, Holden et al. included discussion of the rate of rainfall,’ as
did Peterson and Wallis.* Stern discusses the effect of raindrop sizes and
vertical motion of the walker.’ Bocci approached the question as a
pedagogical means to demonstrate fluxes and flux densities in physics.'°
Mungan and Lipscombe devised a simple cart propelled by rain power
alone.!!
The classical Hollywood musical Singin’ in the Rain suggests a
related question. After working all night, finally discovering how to save
the show-within-a-show, and having fallen in love, Don Lockwood (played
by Gene Kelly) heads home. Even though it is raining torrentially,
Lockwood doesn’t care — even going so far as to give his umbrella to a
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No
passerby. The question now is, how soaked does a walker become if
indifferent to the rain? Or, put differently, how wet does Gene Kelly get?
From the classical world, we know that Philippides brought joyful news to
Athens after the Battle of Marathon, some 26 miles away — collapsing and
dying immediately after announcing the victory over the Persians. Had it
have been raining, how wet would Philippides have become during his
journey?
To answer these questions, we use the familiar structure of the “How
fast should you walk...” problem but make the walker/runner more
realistically human by means of anthropometric formulas. These we
combine with biomechanical models of walking and long-distance running
to determine how wet, and how drenched, Gene Kelly and Philippides
became. Thus, we have a new take on a well-known problem, one that
encourages students to model real-world processes in interdisciplinary ways
by blending physics with biomechanics — a problem that is therefore is of
pedagogical value as well as being of interest for its own sake.
The Water Absorbed By A Moving Block
To begin, consider the walker/runner as a block of height 4, width
w, and breadth b. Suppose further that the walker has speed v and walks in
vertically falling rain of speed wu. In addition, assume that the walker has to
cover a distance L to reach home. Assume all such walkers are human
sponges, who absorb all the water that falls on them, and that the speed at
which they walk is unaffected by the amount of water absorbed. This is the
same model employed in determining how fast someone must run in the
rain to get least wet.
The top of the (bareheaded) walker has an area wd. If the rain falls
with a vertical speed uw, then in a time df, the walker absorbs a mass of rain
dMmrop given by Equation (1):
diyyp =(pwhu) dt, (1)
wherein p is the density of the rain-air mixture. The total amount of rain
absorbed through the top surface is during the journey home of duration
T (= L /v) 1s given by Equation (2):
Te pwhuL .
y
Mrop = Pwhu
(2)
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The mass of water absorbed by the walker through the front surface in time
dt is given by Equation (3):
dM rowr = (Phwy) dt. (3)
The total amount of water absorbed through the front is therefore Equation
(4):
Mipony = PAWL. (4)
The carefree, precipitation-indifferent walker thus absorbs a mass of rain
shown by Equation (5):
m= piu n+) (5)
Vv
A rainfall rate, r, is usually specified in millimeters per hour. In an
hour rain of speed wu m/s travels a distance 3.6 X 10°u millimeters. The
density of the air-rain mixture is thus!” given by Equation (6):
a= Po» (6)
ip
3.6x10°u
where fo 1s the density of water. Light rain corresponds to r = 2.5 mm/hr,
heavy rain has r = 7.5 mm /hr. The world record for the most rain to fall
in one minute belongs to Unionville, Maryland!’ which on July 4, 1956,
experienced 31.5 mm of precipitation in 60 seconds, a phenomenal value of
r= 1,890 mm/hr.
Humanizing The Block
Let us think more about such travelers and “humanize” their
cuboidal physiques. That is to say, we recognize that there 1s a certain subset
of normal body proportions the width of a human being 1s not, for
example, ten times the person’s height — and so h, w, and 6 are not
independent parameters.
Mosteller’s formula'* states that the total body surface area of a
human being, A, in square meters, is given by Equation (7):
peal (7)
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There is also a human aspect ratio, a, so that the shoulder width of
a human, w, is related to height by Equation (8):
Ww
0 = a (8)
As with body mass index, this varies with the person — but it does
not vary by much. For an average male, of height 69.1 inches and shoulder
width of 17.9 inches, a = 0.26. This value is almost constant for people in
the 2.5"" height percentile to the 97.5" height percentile (0.25 to 0.26). For
mathematical simplicity, then, we set it equal to 1/4. (The aspect ratio is
approximately the same for women: an average height of 63.2 inches and
shoulder width of 15.7 inches has a = 0.248.!°)
The total surface area of a cuboidal walker 1s given by Equation (9):
A=2wh+2wb+ 2bh. (9)
Combine this with Mosteller’s formula!®, Eq. (7), and the aspect ratio, Eq.
(8), to obtain Equation (10):
wt Fs ami(142) (10)
6 2 4
This enables us to calculate the best breadth for an ideal humanoid cuboid
as given by Equation (11):
VMh
===, = bn, i
3 | (11)
So, solving for 6 we get Equation (12):
(12)
[As a check, this predicts that a 6’ tall walker with a mass of 80kg (176 Ibs)
has a breadth 5=0.085m and thus a chest measurement (2b + 2w = 2b +
2h/4) equal to 1.07m, or about 42 inches. ]
The mass of rain absorbed by the walker is given by Equation (13):
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m=piv( nem) =pi[ 4442 (13)
So m becomes Equation (14):
ma Pel real a) (14)
4 Sv |3Vh
Walking In The Rain
If walkers do not care about the rain, they will amble along at a
natural pace. One model for walking is that the legs behave like a rigid
pendulum of length Z'’, the time period for which is given by Equation (15):
T=2n pees (15)
8
While such stiff-legged swinging might seem more fitting to model
the walk of the undead in the Zombie Apocalypse, it is a surprisingly good
fit for low-speed human walking. As the leg length is approximately half
the walker’s height!*, we get Equation (16):
r=an/* (16)
ag
Pedometer instructions!’ report that step length is 0.415/ which, to within
1%, 1s = h, and thus we get Equation (17):
J3gh
y=. 17
ce (17)
This predicts, as a check, a walking speed of 0.6 ms! (about 1.3 mph) for a
1.8m (6’) tall walker.
The mass of water accumulated by a person strolling in the rain 1s,
by combining Eqs. (14) and (17), given by Equation (18):
= Ply «AS |
m= c es xvi j |) (18)
4
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To estimate this value, we use meteorological data. The speed of falling
rain, u, depends on the size of the raindrops, but a good estimate 1s
approximately 5 m/s”’. Thus we get Equation (19):
[Su I
soe aeo8
To a reasonable level of approximation we have Equation (20):
m= El ween tf —4)) (20)
4 3V h
This is the equation that describes the mass of water absorbed by someone
of height A strolling a distance L in rain of density p.
=. OS: (19)
To compare these results, we follow Holden ef al. and consider
heavy rainfall, so that r=10 mm/h. During a 100-meter journey the walker
absorbs a mass of water equal to Equation (21):
m=a(m-2.778" +22 Vi | (21)
There is, though, a problem. Namely, the mass of a person is not
independent of their height. Hence in medicine, one usually speaks of the
body mass index (BMI), as defined by Equation (22):
M
Baa. (22)
Hence?! m becomes Equation (23):
| ee ae (23)
12 3
This allows us to look at water absorption based on body type. An
underweight person has a BMI of 16; a person in the middle of the normal
weight range for their height has a BMI of 21.7; an overweight person has
a BMI of 25; and a BMI of 30 or more is the clinical definition of obese.
For two walkers of the same height, the one with the larger body mass index
will get wetter. This is logical, as the speed at which they walk depends only
on their height and is thus the same for both walkers, whereas the person
with the higher body mass index will have a larger rain-collecting surface
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area. By the same reasoning, for two walkers with the same body mass
index, the taller one will become less wet, for their walking speed means
they get home far more quickly, thus exposing them to less rain.
Numerically, if we assume a |.8 m-tall walker (6’) with a body mass
index in the middle of the ideal range (21.7), and hence a mass of 70.3 kg,
the equation predicts absorption of 0.05 kg of water. This is close to the 0.06
kg calculated by Peterson and Wallis for a walker hustling to get home at a
speed of | ms’. Figure | presents the mass of water absorbed as a function
of height for various values of the body mass index.
Water absorbed as a function of height
“— »
E << = *
eS ee *
a e ® 2
8 0.06 a on cer
= eoe?®* e @ 3°
= e«? Pe
co os =
¥ 00 » °° —ate-e* is @BMie18.5
r= >
S id
gee” @5Mi=21.7
® 0.04
© @6Mi=30
> 00
0.01
15 1.6 OF 18 hook 2 21
Height (m)
Figure |
As an example, Gene Kelly was 1.71 meters tall and had a mass of
70 kg”. Hence his BMI was 23.94. Thus, as he danced his way home in
heavy rain, he absorbed about 0.07 kg of water during the first 100 meters
of his journey. In contrast, his co-star, Debbie Reynolds, was 1.57 m tall
and weighed 51 kg” and thus had a BMI of 20.69. She would have absorbed
Fall 2017
a mass 0.057 kg, only 80% of the amount that Gene Kelly did, had she taken
part in the song-and-dance number, Singin’ in the Rain.
This suggests there is another quantity worth considering. Namely,
we introduce a drenching factor A, which is the ratio of the water absorbed
to the walker’s weight. Thus we get Equation (24):
G = 2.77? ATT iF |
omens
G =2.77h” ATT Bh
_ pl 3 al
4 Bh’
The implication is clear. The longer your journey home, or the
heavier the rain, the more drenched you become. For two people of the same
height, the person of higher mass or larger body mass index is less drenched.
For two people of the same mass or body mass index, the taller person 1s
less drenched.
Running In The Rain
Philippides ran from Marathon to Athens to convey news of the
Greek victory over the Persians**. He would have done so whether the
weather be hot or not. What if it had been raining? Again, we can think of
him absorbing water rather like a block, but instead of walking, he runs a
long distance. The speed of long-distance running is determined, as per
Banks, through energy considerations. Philippides generates heat
proportional to his kinetic energy. Hence, he produces heat energy E,
governed by Equation (25):
E, =k My’. (25)
Here, kg is a constant related to heat gain.
From Newton’s law of cooling, Philippides loses heat energy E,
through his surface area, so that we get Equation (26):
k, Mh
E,=k,A= ram (26)
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-]
(The dynamics of weight loss has likewise been modeled by energy loss
proportional to human surface area.*°) A reasonable model for long-distance
running, then, is that these two energies must balance, in which case we get
Equation (27):
k,Mv* = (27)
k, Mh
6 5
so that v? becomes Equation (28):
eas follhgws fo peta (28)
6k, VM 6k, V Bh
As a plausibility argument, this equation predicts that successful
long-distance runners are likely to be relatively short and slight of build.
Men’s marathon record holder Dennis Kipruto Kimetto is 1.71 m tall, which
is below average height, and with a mass of 55 kg has a BMI of 18.8.
Sprinter Usain Bolt is 2m tall and has a mass of 93.9 kg, for a BMI of 24.5.
These BMIs are at the low and the high end, respectively, of the range of
“normal” BMIs.
The mass of water absorbed when running a (long) distance L 1s,
from Eq. (14) and Eq. (28), given by Equation (29):
ma Pll et (2) (2 fa] (29)
4 s¥k (nh) \3Va
Or, in terms of body mass index, m becomes Equation (30):
6k
m= ae ae —h(Bh) Be = | (30)
l
As before, for two runners of the same height, the heavier runner or
the one with higher body mass index, will absorb more rain, a consequence
of having a larger surface area.
To obtain a numerical estimate, Kimetto’s world record is 2:02:57
for the 42.195 km race. Using his data we get Equation (31):
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(SP) - A os (31)
Sih) Gh Ne
So that it becomes Equation (32):
See. (32)
6k,
(There are, naturally, some problems in assuming that this number is the
same for all athletes and setting its value based on the world record holder.
Italy’s Stefano Baldini holds the 485" fastest marathon time and has a mass
of 162 kg and a height of 1.76 m, which gives a ratio of 180.6. There is
variation, then, among elite runners, but the percentage variation 1s slight.)
Hence, for long-distance road runners 1n the rain, Eq. (30) and Eq.
(32) predict Equation (33):
h( Bh)" Runa
fea 33
4 13262 a
Over the course of 100 meters of the race, in rain where r=10 mm/h,
the water absorbed is given by Equation (34):
Dells
. h( Bh)" Bh]
—— (34)
70 13.62
Figure 2 shows the mass of water absorbed during the course of 100
meters run.
_This does not depend appreciably on the body mass index of the
runner. This may seem surprising, since for two runners of the same height,
the one with lower body mass runs more swiftly and has a lower surface
area through which to absorb rain. However, there is a critical height or
body mass ratio, for which the term in brackets is zero. This occurs when
M is given by Equation (35):
M=9h’, (35)
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corresponding to a critical body mass index given by Equation (36):
B =n. (36)
crit
Water absorbed per 100m run
Water absorbed (kg) per 100m run
15 16 17 18 19 2 21
he
Height of rummer (m)
@BMili85 @BMr217 #830
Figure 2
Such a runner absorbs a “critical mass” of water given by Equation (37),
h?
bee (37)
This 1s, 1n essence, the curve shown 1n Figure 2. Runners with a BMI
less than 9h will absorb less than this amount; runners with a BMI greater
than the critical value will absorb more water. The Center for Disease
Control defines the “underweight” category to be a BMI of 16. Hence, a
runner of height 1.78 m has a critical BMI of 16.02, and so a slightly
underweight runner will be below the critical value. An exceedingly tall
runner, of height 2.06m (about 6’ 8”), has a critical BMI of 18.5, which
corresponds to a “normal” weight for their height. In other words, most
reasonably fit runners will have a BMI close to the critical value and, as a
consequence, will absorb an amount of water equal to the critical mass.
The drenching ratio is given by Equation (38):
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ens 1/4
poe on =) ee
(38)
4 M
Or, in terms of BMI it is given by Equation (39):
; 6k,
h += |—2h( Bh)" Bh 1
= (39)
4 Bh’
Numerically, over 100 meters of the race 1t becomes Equation (40):
G +h(Bh)- Nah -])
AS (40)
We 13.62Bh™
Namely, for runners of the same height, the heavier runner 1s less drenched.
Conclusion
This article has explored how wet people become if, when going
somewhere in the rain, they do not care whether they get soaked or not. This
is closely related to the well-known problem of how fast to walk in the rain
to get least wet. When indifferent to the rain, and thus walking at a natural
pace, 1f two walkers are in the same overall shape, as measured by body
mass index, the taller walker will be less wet. Taller walkers have a faster
pace, which gets them indoors more swiftly than a slower walk, and this
more than compensates for their larger surface area.
Those who run long distances, though, have a different effect. While
those of lower body mass index should be able to run more swiftly and have
a lower surface area exposed to precipitation, the effect 1s barely noticeable.
The sole determining factor is not whether you are underweight or obese,
but how tall you are. Taller runners become wetter. Shorter runners will
remain drier than shorter walkers, but extremely tall runners may get wetter
than their low body mass index walking counterparts.
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' B.L. Schwartz and M.A.B. Deakin “Walking in the rain, reconsidered” Mathematics
Magazine 46(5) 246-53, 1972 corrects Michael. A. B. Deakin’s earlier “Walking in the
rain” Mathematics Magazine 45(5), 246-53. The former views the problem as an
interesting pedagogical case for mathematics students of minimizing the function |x|.
David E. Bell “Walk or Run in the Rain?” Mathematical Gazette. 60 No. 413 206-208
(1976).
> Mark J. Volkmann’s “To walk or run in the rain: A geometric solution” School Science
and Mathematics 93(4) 217-20 is suitable for high-school students and introduces the
fictional cartoon character Cubo, who could be replaced in modern classrooms by
Spongebob Squarepants.
4 Herb Bailey “On running in the rain” College Mathematics Journal 33(2) 88-92
dissents. He looks at the maxima and minima of the functions involved and thinks that
sometimes, even with the wind at one’s back, it is best to head home at top speed. Bailey
might be the first of those who studied the problem to consider a female walker.
> Dank Hailman and Bruce Torrents (a.k.a. Dan Kalman and Bruce Torrence) “Keeping
dry: The Mathematics of running in the rain”. Mathematics Magazine 82(4) 266-77,
2009.
® Robert B. Banks Slicing Pizzas, Racing Turtles, and Further Adventures in Applied
Mathematics. (Princeton: Princeton University Press, 1999). See chapter 12, “How Fast
should you run in the rain”, pp 114—122.
7 J.J. Holden, S.E. Belcher, A. Horvath, and I Pitharoulis “Raindrops keep falling on my
head” Weather 50(11) 367-70.
8 Thomas C. Peterson and Trevor W. R. Wallis “Running in the rain” Weather 52(3) 93—
Go19o7
? §. A. Stern “An optimal speed for traversing a constant rain.” American Journal of
Physics 51(9) 813-818 (1983).
!0 Franco Bocci “Whether or not to run in the rain” European Journal of Physics 33(5)
1321-322, (2012).
'! Carl E. Mungan and Trevor C. Lipscombe “The Rain-Powered Cart” European
Journal of Physics 37(5) 2016 055005
'2 Neglecting the density of the air, which is a mere fraction of the density of water.
'3 Howard H. Engelbrecht and G.N. Brancato “World Record One-Minute Rainfall at
Unionville, Marlyand” Monthly Weather Review, August 1959, p. 303-306.
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'4 RD. Mosteller “Simplified Calculation of Body-Surface Area,” New England Journal
of Medicine 317(17) 1987, p. 1098. There are other formulas to model body surface
area, but Mosteller’s is mathematically the simplest.
'S See illustration at http://www. learneasy.info/MDME/MEMmods/MEM30008A-
EcoErgo/Ergonomics/Ergonomics.html
'© Mosteller’s formula, one might argue, is dimensionally incorrect. This is resolved by
. . . . os . 5/9
considering the 6 in the denominator as a normalizing physical constant, 6 kg!” m*”, to
ensure correct dimensions.
'? See, for example, Trevor Davis Lipscombe The Physics of Rugby (Nottingham:
Nottingham University Press, 2009), p. 36.
'8 G J Slater, A J Rice, I Mujika, A G Hahn, K Sharpe, D G Jenkins “Physique traits of
lightweight rowers and their relationship to competitive success” Br J Sports Med
2005;39:736—741 has measurements of L/h for 62 elite male rowers, with an average
value of 0.527, and 45 elite female rowers with a ratio of 0.531.
' http://livehealthy.chron.com/determine-stride-pedometer-height-weight-45 18.html
°° As per Holden ef al., vide supra.
*! As with the Mosteller formula, there are dimensional issues. If we regard the
denominator as being not M but 1M, where | is a physical constant whose dimensions
are m’ kg", the units become correct.
*? http://starschanges.com/gene-kelly-height-weight-age/
23 http://www.bodymeasurements.org/debbie-reynolds/
4 Tradition, and Herodotus (in The Histories, 6.105.1), credits Philippides for this feat,
and Lucian tells it this way in A Slip of the Tongue in Greeting. Plutarch reports, in The
Glory of the Athenians, that “most historians declare that it was Eucles who ran in full
armour, hot from the battle, and, bursting in at the doors of the first men of the State,
could only say, ‘Hail! we are victorious!’ and straightway expired.” See Plutarch, “de
gloria Atheniensium” in Moralia Vol. IV. Translated by Frank Cole Babbitt.
(Cambridge: Harvard University Press, 1936) p. 505. For a fuller discussion, see John
Haberstroh “Philippides: Famed Marathon Runner?” Presentation, Missouri Valley
History Conference, March, 2013, online at
https://www.academia.edu/4924439/Philippides Famed Marathon Runner
°° Carl E. Mungan and Trevor C. Lipscombe “A Physics Model for Weight Loss by
Dieting” Latin American Journal of Physics Education 6(3) (2012): 344-346
Washington Academy of Sciences
Bio
Trevor Lipscombe is the director of the Catholic University of America
Press. He is the author of "The Physics of Rugby" (Nottingham University
Press, 2009); coauthor, with Alice Calaprice, of "Albert Einstein: A
Biography" (Greenwood Press, 2005); and editor of the critical edition of
Blessed John Henry Newman's novel "Loss and Gain" (Ignatius Press,
2012).
Fall 2017
Washington Academy of Sciences
Description of a New Species of Cestode Parasitic
Worm from an Indian Scops Owl in Mizoram, India
Suranjana Banerjee', Buddhadeb Manna’, and A. K. Sanyal !
'Zoological Survey of India, M-Block, New Alipore, Kolkata -700053, India
*Parasitilogy Research Unit, Department of Zoology, University of Calcutta, Kolkata,
India
Abstract
We report a new genus Gyrocoelia Fuhrmann, 1899 from Mizoram, India.
In 2007 an Indian Scops Owl (Ottus bakkamoena) was procured from a
local man in Mizoram, India. On close examination the bird was found to
be infected with a new cestode species of the genus Gyrocoelia Fuhrmann,
1899. The genus Gyrocoelia Fuhrmann, 1899 has only five known species.
The newly described species named Gyrocoelia mizoramensis 1s
characterized by a globular scolex; rostellum bearing single crown of 128
hooks arranged in 16 loops; multilobulated ovary and a large seminal
receptacle differentiating it from the rest of previously described species.
Introduction
THE GENUS GYROCOELIA was established by Fuhrmann in 1899. Khalil
et al. (1994) synonymized the genus Bothriocephalus Linstow (1906)
with Gyrocoelia. The type species of this genus 1s Gyrocoelia perversa
Fuhrmann, 1899 collected from Actophilus africanus from Africa. The
other known hosts of the type species are Himantopus himantopus,
Hoplopterus spinosus, Limosa rufa and Vanellus sp. The following
species under the genus Gyrocoelia have been synonymized with other
species:
1. G albaredai Lopez-Neyra, 1952 and G. polytestis Saakova, 1952
have been synonymized with /nfula burhini Burt, 1939.
2. G. australiensis (Johnston, 1910) Johnston, 1912 and G. kiewietti
Ortlepp, 1937 have been synonymized with G. coronata Krefft,
S745
3. G. brevis Fuhrmann, 1900, G. milligani Linton, 1927, G. fausti
Tseng, 1933 and G. fuhrmanni Rego, 1968 have been synonymized
by Schmidt (1986) with G. crassa (Fuhrmann, 1900) Baer, 1940.
Fall 2017
18
Currently the following known species are present under the genus
Gyrocoelia Fuhrman, 1899:
1. Gyrocoelia coronata Krefft, 1871; Host: Himantopus
leucocephalus from Australia.
2. Gyrocoelia crassa (Fuhrmann, 1900) Baer, 1940; Host: Aegialitis
collaris from Egypt.
3. Gyrocoelia pagollae Cable and Myers, 1956; Host: Pagolla
wilsonia from Puerto Rico.
4. Gyrocoelia perversa Fuhrmann, 1899; Host: Actophilus africanus,
Himantopus himantopus, Hoplopterus spinosus, Limosa rufa and
Vanellus sp., from Africa.
5. Gyrocoelia paradoxa Linstow, 1906; Host: Aegialitis mongolica
from Philippines.
Our goal is to add a new cestode species discovered in a vertebrate host
(Ottus bakkamoena) 1n Mizoram, India.
Material and Methods
During a study tour to collect cestode parasites from vertebrate
hosts in Mizoram, India a bird (Ottus bakkamoena) with ruffled plumage
was procured from a local in North Khawbung district in Aizawl,
Mizoram. The bird was examined for parasites in 2007. The bird was
euthanized with ethanol in a closed jar following the protocol of Ghosh
and Kundu (1999). The protocol of Ghosh and Kundu (1999) is followed
as per local standard collection procedure of cestode parasites for infected,
sick birds.!
A cotton swab of a few drops of ethanol was used for
anaesthetization. The necropsy was performed under a stereoscopic
microscope. The bird was dissected and the entire alimentary canals were
removed and internal organs such as liver, heart, lung, kidney, and urinary
CPCSEA Guidelines for Laboratory Animal Facility: GUIDELINES ON THE REGULATION OF
SCIENTIFIC EXPERIMENTS ON ANIMALS Ministry of Environment & Forests (Animal Welfare
Division) Government of India, June 2007.
Washington Academy of Sciences
19
bladder were placed into normal saline in petri dishes and examined under
a field binocular separately in different petri dishes (Justine e/ al., 2012).
We found that the bird was infected with two cestode specimens
of the genus Gyrocoelia Fuhrmann, 1899. The cestode specimens were
collected from the intestine of the host, pressed and flattened between two
slides, and preserved in 70% alcohol in a glass vial. They were then
dehydrated in increasing concentrations of alcohol, stained in alcoholic
borax carmine, cleared in xylol, and mounted on slides in Canada balsam
(Ghosh and Kundu, 1999). The specimens were studied under a
microscope (Magnus MLX-Trinoculor from Olympus, Japan) and camera
lucida drawings and photomicrographs were made to describe the species
in detail.
Results
We have isolated a new species of Gyrocoelia mizoramensis (Figs.
| and 2) with the characteristics of the genus Gyrocoelia Fuhrmann, 1899.
The parasites are medium in length and the body consists of scolex, neck,
immature, mature, and gravid proglottids. The segments are almost square
in shape. Segmentation is craspedote. Immature proglottids are longer
than they are broad, while the mature and gravid proglottids are broader
than they are long. As the proglottids mature progressively the ratio
between the length and breadth decreases, and the proglottids appear to
be square. All the measurements given are in millimeters unless otherwise
mentioned in the text.
The immature proglottids measure 0.11-0.16 in length and 0.09-
0.12 in breadth. The mature proglottids measure 0.12-0.13 in length and
0.26-0.27 in breadth. The gravid proglottids measure 0.16-0.27 in length
and 0.31-0.34 in breadth. The parasite measures 19.65-22.13 in length and
0.32-0.34 in breadth.
Head region: The scolex is globular in shape, slightly set off from the
neck and measures 0.06-0.15 in length and 0.06-0.13 in breadth. The
scolex is provided with four slightly oval and unarmed suckers measuring
0.03-0.05 in length and 0.02-0.05 in breadth. The rostellum is everted
measuring 0.06-0.07 in length and 0.1-0.13 in breadth. The rostellum
bears a single row of 128 hooks arranged in 16 loops, each loop with eight
hooks. There are seven loops on each of its dorsal and ventral surfaces
Fall 2017
20
and one loop on each of its lateral faces. Each hook has a relatively long
handle and small guard and blade. The hook is bifurcated. The blade is
0.47-0.51 long. Each loop measures 0.03-0.04 in length and 0.04-0.06 in
breadth. The neck is short and broad and measures 0.42-0.63 in length and
0.06-0.07 in breadth.
Testicular region: The testes are round to oval in shape, 27-30 in number,
measure 0.03-0.04 in length and 0.04-0.05 in breadth, mostly postovarian
while some are present on the two lateral sides of the ovary. The cirrus
sac is elongated, slightly oblong and crosses the dorsal osmoregulatory
canals. It measures 0.27-0.3 in length and 0.02-0.03 in breadth. The cirrus
is unarmed, everted in most of the proglottids and measures 0.2-0.21 in
length and 0.02 in breadth. The vas deferens 1s coiled and thick-walled.
There is no external or internal seminal vesicle. The genital pores alternate
regularly except in a few proglottids where the genital pores are unilateral.
The genital pores are situated in the anterior part of the lateral margin of
each proglottid. The genital atrrum measures 0.08-0.11 in length and 0.11-
0.14 in width.
Uterine region: The ovary lies in the posterior portion of the proglottid.
It is single massed, consists of numerous lobes arranged almost fanwise
measures 0.1-0.12 in length and 0.16-0.3 in width. There is no ootype.
The vagina is a thin tube, arises from the ovary, runs for a very short
distance and then dilates into a round seminal receptacle, measuring 0.1-
0.12 in length and 0.1-0.14 in breadth in the middle of the proglottid. It
then extends as a straight tube from the seminal receptacle and opens
posterior to the cirrus sac into the common genital atrium. The uterus
appears as a sac but later ruptures and the eggs are entirely released into
the proglottids.
Post ovarian region: The vitelline gland is small, compact, and lies
posterior to the ovary. It measures 0.4-0.05 in length and 0.07-0.08 in
breadth. Each egg is round in shape and has a diameter between 0.02-0.05.
The osmoregulatory canals are four in number, two dorsal and two ventral.
Washington Academy of Sciences
2]
Data Summary
Type specimens. Holotype (One specimen in one slide with the
Zoological Survey of India Accession number W9943/1; one paratype
specimen is also present in the same slide.)
Deposition. Deposited in Platyhelminthes Section, Zoological Survey of
India, New Alipur, Kolkata-53, India
Type host. Oftus bakkamoena
Site of infection. Intestine
Type locality. Aizawl (Latitude: 23.7271° N, Longitude: 92.7176° E)
Mizoram, India
Prevalence. |/2
Etymology. The specific epithet 1s derived from the name of the state of
Mizoram from where it had been recovered.
Discussion
Summarizing the data we note that the present observed species
measures 19.65-22.13 in length and 0.32-0.34 in breadth; scolex globular,
measures 0.06-0.15 in length and 0.06-0.13 in breadth; suckers four in
number, oval, measures 0.03-0.05 in length and 0.02-0.05 in breadth;
rostellum measures 0.06-0.07 in length and 0.1-0.13 in breadth , bears a
single crown of 128 hooks arranged in 16 loops, each loop carries 8 hooks;
neck short; segmentation craspedote; testes 27-30 in number, oval in
shape, cirrus sac long and elongated, measures 0.27-0.3 in length and
0.02-0.03 in breadth; cirrus unarmed; genital pores regularly alternate or
unilateral; genital atrium deep, measures 0.08-0.1 in length; ovary
multilobulated, lies posteriorly, irregular in shape; vagina 1s a thin tube;
seminal receptacle large, round in shape; vitelline gland small, compact,
dorsolateral to the ovary; uterus tubular; egg round and diameter is
between 0).02-0.05.
The observed species comes closer to G. pagollae Cable and
Meyers, 1956 in number of testes, presence of a short neck and a fan-
shaped ovary. The observed species differs from G. pagollae Cable and
Meyers, 1956 in not having 66 rostellar hooks; dioecious strobila; spines
Fall 2017
in the cirrus; and a V-shaped vitelline gland and absence of seminal
receptacle and a genital atrium.
Table 1. A comparative account of the morphological characters of
the valid species under the genus Gyrocoelia Fuhrman, 1899
G.coronat
a Krefft,
1871
cs
Himantop
us
Host
leucoceph
alus
Chara
cteristi
1940
Body
Length
(L) and
Breadt
h (B)
Scolex
Length
(L) and
Breadt
h(B
Sucker
S
Length
(L) and
Breadt
h (B)
Rostell
um
Length
(L) and
Breadt
h (B)
Numbe
r of
rostella
rt loops
Numbe
r of
hooks
in each
loo
G.crassa
(Fuhrmann,
1900) Baer,
Aegialitis
collaris
Dioccious Dioecious nee
L=50-62.7
(male)
L=100.0
(female)
G.paradoxa
Linstow,
1906
G.perversa
Fuhrmann,
1899
G.pagollae
Cable and
Myers,
1956
Pagolla
wilsonia
rufinucha
Aegialitis
mongolica
Actophilus
africanus
G.mizoram
ensis n.sp.
Ottus
bakkamoen
a
Male and
Female in
same strobila
Male
1=30.0
Female
L=75.0
L=0.14
B near tip=
0.063-0.067
B near base
Male and
female in
same
strobila
8 hooks in
cach loop
Total hooks
= 128
Washington Academy of Sciences
23
Length
of hook
Testes
Numbe
r (N),
Length
(L) and
Breadt
Length of
L= 0.040 L=0.029 blade =
0.468-0.507
Absent Very short Absent Absent Short,
broad
(N):20-30
G.P:Irregul
arly
alternate,
unilateral or
(N): (27-
(N)i GAP (IN)? 33 (GPs 30) GP:
Irregularly Regularly Regularly
alternate alternate alternate
(N):60 -76
L= 0.080
B= 0.038
h (B) ;
Genital Pree
Bure alternate
(G.P)
Male
strobila
L=0.520
Male strobila:
Cirrus
sac B=0.150 Teor L=0.27-0.3
Length Cirrus B=0. 16-0.18 B=0.02-
(i) and 6.900 Female | 2" Gaol
Breadt ; Female P not spined
strobila:
Hee) Cirrus spined
Strobila:
L=0.765
B=0.207
Semina
|
Recept
acle
(S.R)
Vagina
(V)
Genital
Atrium
S.R: absent
(V): absent
S.R: absent
(V):absent
G.A:Presen
t
WAG
G.A:Presen ; L=0.04-
t G.A:Present 0.05
B=0.07-
0.08
Transversel
Transversely se tubular Tubular Transversel
tubular with y clongated
diverticula
B=0.036
Remarks: (—) indicates data not available in original description
(G.A.) G.A:Presen
Vitellin G.A:Absent; ts
e Gland V.G: V.G:V-
(V.G) L=0.112x0.42 | shaped
Length transversely
(L) and , elongated
Breadt
Fall 2017
Acknowledgements
The authors are thankful to the Director Zoological Survey of India for
providing necessary facilities during the course of the work. The authors
would also like to express their deepest thanks to the Library Division of
Zoological Survey of India, Kolkata- HQ for providing necessary
facilities.
References
Baer, J.G. (1940). Some avian tapeworms from Antigua, Parasitology
32 (2): 174-197 (Thirty seven figures).
Burt, D.R.R. (1940). New avian cestodes of the family Davaineidae
from Ceylon. Ceylon Journal of Science 22: 65-77.
Cable, R.M and Meyers, R.M. (1956). A dioecious species of
Gyrocoelia (Cestoda:Acoleidae ) from the naped plover. Journal
of Parasitology 42(5): 510 -515.
Fuhrmann, O. (1899). Deux singuliers Taenias d’ oiseaux: Gyrocoelia
perversus n.g. n.sp. et Acoleus armatus n.g. n.sp. Rev. Suisse Zool,
7: 341 —451.
Fuhrmann, O. (1900). Neue eigentumliche Vogel cestoden
Eingetrenntge-schlechtlicher cestode. Zool. Anz. 23: 48-51.
Ghosh, R.K. and Kundu, D.K. (1999). Fauna of Meghalaya (Cestoda).
Zoological Survey of India, State Fauna Series 4 (Part 9): 247-281.
Johnston, T.H. (1910). On Australian avian Entozoa. Proceedings of the
Royal Society New South Wales 44: 84-122.
Johnston, T.H. (1912). New species of cestodes from Australian birds.
Memoirs Queensland Museum 1: 211-215.
Justine, J.L., Briand, M., Rodney, A. and Bray, R.A. (2012). A quick
and simple method, usable in the field, for collecting parasites in
suitable condition for both morphological and molecular studies.
Parasitology Research, Springer Verlag (Germany) 111 (1): 341-
Spill
Washington Academy of Sciences
Ze
Khalil, L.F., Jones, A and Bray, R.A. (1994). Keys to the cestode
parasites of vertebrates. CAB International, /nternational Institute
of Parasitology, UK: xiii + 751.
Krefft, G. (1871). On Australian Entozoa.Trans.Entom. Soc. New South
Wales 2: 206-232.
Linton, E. (1927). Notes on cestode parasites of birds. Proc. U.S. Nat.
Mus. 70 (7): 1-73 (15 plates).
Linstow, O.F.B. (1906). Helminthes from the collection of the Colombo
museum, Spolia Zeylonica 3: 163-188. (3 plates).
Lopez-Neyra, C.R. (1952).Gyrocoelia albaredai n. sp. Relaciones com
Tetrabothriidae y Dilepididae.Rev. Iber. Parasit. 12 (4): 319-344,
(3 plates).
Ortlepp, R.J. (1937). South African helminths.Part I. Onderstepoort. J.
Vet. Sc. Anim. Ind. 9: 311-366.
Rego, A.A. (1968). Sobretres cestodeos de aves Charadriiformes. Mem.
Inst ©. €ruzi66; 107-115.
Schmidt, G.D. (1986). CRC Handbook of Tapeworm Identification,
CRC Press Inc. Boca Raton, Florida: 1-675.
Saakova, E.O. (1952). Reference collected from website Global cestode
database for Gyrocoelia polytestis.
Tseng, S. (1933). Studies on avian cestodes from China. Part II.
Cestodes from Charadriuform birds. Parasitology 24: 500-511.
Fall 2017
Wwwig?D
WwUEg'd
O96 29% @
98 %@®
Figure 1. Camera lucida drawings of Gyrocoelia mizoramensis n.sp. isolated
from Ottus bakkamoena
(a) Scolex (b) Mature proglottid (c) Spine
Washington Academy of Sciences
Figure 2. Photomicrographs of Gyrocoelia mizoramensis n.sp. isolated from
Ottus bakkamoena
(a) Scolex (b) Mature proglottids (c) Gravid proglottids
Fall 2017
Bios
Dr. Suranjana Banerjee M.Sc., Ph.D. in Zoology is a Senior Zoological
Assistant in the Zoological Survey of India. Her field of interest includes
research in morphology, taxonomy and systematics of cestodes. She
acquired her Ph.D. degree on her work on Taxonomy of Cestodes from
Eastern and North Eastern States of India. She has discovered several new
species of cestodes from India. Apart from her major field of interest in
cestode taxonomy, her other areas of interest include taxonomy of soil
nematodes and insects of the order Odonata. She has published more than
15 research papers in national journals.
Dr. Buddhadeb Manna, Emeritus Professor and Head (Ret.),
Department of Zoology, University of Calcutta, 1s engaged in research in
Parasitology. As many as seven students got a Ph.D. from Calcutta
University under his able guidance. He has published nearly 216 research
articles in different journals of international repute.
Dr. Asok Kanti Sanyal M.Sc., Ph.D. in Zoology was retired Director-in-
charge and Emeritus Scientist in Zoological Survey of India. He received
training on EIA, Biodiversity Conservation and SEM in U.K. and
Singapore. He has 40 years of working experience on taxonomy and
ecology of soil microarthropods, acarology, nematology, wildlife, and
biodiversity and has discovered over 130 species of mites and nematodes
from India and Antarctica. He has published several books and more than
220 scientific papers in national and international journals. He is also
amongst the very few to have made an Expedition to Antarctica from the
Zoological Survey of India. Several scholars have been awarded the
M.Phil. and Ph.D. degree under his supervision.
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1200 New York Ave. NW
Washington, DC 20005
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HARVARD LAW SCHOOL LIBRARY ERSMCZ
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