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MAMMALS 

OF 
MARYLAND 


FAUNA 


NUMBER  66 


UNITED  STATES 

DEPARTMENT  OF  THE  INTERIOR 

BUREAU  OF  SPORT  FISHERIES  AND  WILDLIFE 


JCCIDENTAI  COLU^ 


iji.,1 


.jkARY 


vC-  ^'^'r'^\  ■  y 


NORTH  AMERICAN  FAUNA 


This  publication  series  includes  monographs  and  other  reports  of  scientific  in- 
vestigations relating  to  birds,  mammals,  reptiles,  and  amphibians,  for  professional 
readers.  It  is  a  continuation  by  the  Bureau  of  Sport  Fisheries  and  Wildlife  of  the 
series  begun  in  1889  by  the  Division  of  Ornithology  and  Manunalogy  (Department 
of  Agriculture)  and  continued  by  succeeding  bureaus — Biological  Survey  and  Fish 
and  Wildlife  Service.  The  Bureau  distributes  these  reports  to  official  agencies,  to 
libraries,  and  to  researchers  in  fields  related  to  the  Bureau's  work;  additional 
copies  may  usually  be  purchased  from  the  Division  of  Public  Documents,  U.S. 
Grovemment  Printing  Office. 

Reports  in  North  American  Fauna  since  1950  are  as  follows  (an  asterisk  indi- 
cates that  sale  stock  is  exhausted ) : 

•60.  Raccoons  of  North  and  Middle  America,  by  Edward  A.  Goldman.  1950.  153  p. 

*61.  Fauna  of  the  Aleutian  Islands  and  Alaska  Peninsula,  by  Olaus  J.  Murie; 
Invertebrates  and  Fishes  Collected  in  the  Aleutians,  1936-38,  by  Victor  B. 
SchefFer.  1959.  406  p. 

*62.  Birds  of  Maryland  and  the  District  of  Columbia,  by  Robert  E.  Stewart  and 
Chandlers.  Robbins.  1958.  401  p. 

*63.  The  Trumpeter  Swan;  Its  history,  habits,  and  population  in  the  United 
States,  by  Winston  E.  Banko.  1960.  214  p. 

*64.  Pelage  and  Surface  Topography  of  the  Northern  Fur  Seal,  by  Victor  B. 
ScheflFer.  1961.  206  p. 

65.  Seven  New  White-winged  Doves  From  Mexico,  Central  America,  and  South- 
western United  States,  by  George  B.  Saunders.   1968.   30  p. 


MAMMALS 

OF 
MARYLAND 


By 
John  L.  Paradiso 


NUMBER  66 


""'"™**NT  DMUMEKTS  ilEPARTWf  MT ! 

)   MAR  3  1  2000 


UNITED  STATES 

DEPARTMENT  OF  THE  INTERIOR 

Walter  J.  Hickel,  Secretary 

BUKEAU  OF  SPORT  FISHERIES  AND  WILDLIFE 
John  S.  Gottsohalk,  Director 


North  American  Fauna,  Number  66 

Published  hy 

Bureau  of  Sport  Fisheries  and  Wildlife 

April  1969 


United   States   Government   Printing   Office      •       Washington       •      1969 


For  sale  by  the  Superintendent  of  Documents,  U.S.  Government  Printing  OflSce 
Washington,  D.C.  20402  -  Price  $1 


CONTENTS 


Page 

Introduction 1 

Location  and  area  of  Maryland 2 

Temperature 3 

Average  annual  precipitation 3 

Effects  of  civilization 4 

Principal  biotic  or  natural  areas  in  Maryland 4 

Eastern  Shore  section 5 

Western  Shore  section 6 

Piedmont  section 7 

Ridge  and  Valley  section 7 

Allegheny  Mountain  section 7 

Maryland's  mammalian  fauna 8 

Keys 9 

Accounts  of  species 14 

Order  Marsupialia  (pouched  mammals) 14 

Order  Insectivora  (shrews,  moles,  etc.) 15 

Order  Chiroptera  (bats) 41 

Order  Lagomorpha  (rabbits,  hares,  etc.) 61 

Order  Rodentia  (gnawing  mammals) 67 

Order  Camivora  (flesh-eating  mammals) 130 

Order  Artiodactyla  (even-toed  hoofed  mammals) 167 

Marine  mammals  of  Maryland 173 

Extirpated  Recent  mammals  of  Maryland 181 

References 184 

MAPS 

Page 
Figure     1.  Map  of  Maryland  showing  the  23  counties,  Baltimore  City, 

and  the  District  of  Columbia 3 

2.  Physiographic  provinces  of  Maryland 5 

3.  Biotic  sections  of  Maryland 6 

4.  Distribution  of  Sorex  cinereus  fontinalis  and  S.  c.  cinereus 17 

5.  Distribution  of  Sorex  longirostris  longirostris 21 

6.  Distribution  of  Sorex  fumeus  fumeus 24 

7.  Distribution  of  Sorex  dispar  dispar 26 

8.  Distribution  of  Microsorex  hoyi  winnemana 27 

9.  Distribution  of  Blarina  brevicauda  kirllandi 29 

10.  Distribution  of  Cryptotis  parva  parva 33 

11.  Distribution  of  Parascalops  breweri 35 

12.  Distribution  of  Scalopus  aquaticus  aquaticus 37 

13.  Distribution  of  Condylura  cristata  cristata 40 

14.  Distribution  of  Myotis  lucifugus  lucifugus 42 

15.  Distribution  of  Myotis  keenii  septentrionalis 44 

16.  Distribution  of  Myotis  sodalis 45 

ni 


IV 


CONTENTS 


Figure 


17. 
18. 
19. 
20. 
21. 
22. 
23. 
24. 
25. 
26. 
27. 
28. 
29. 
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31. 
32. 
33. 
34. 

35. 
36. 
37. 

38. 

39. 
40. 
41. 
42. 
43. 
44. 
45. 
46. 
47. 
48. 
49. 
50. 
51. 
52. 
53. 
54. 


Distribution  of  Myotis  subulatus  leibii 

Distribution  of  Lasionycteris  noctivagans 

Distribution  of  Pipistrellus  subflavus  subflavus 

Distribution  of  Eptesicus  fuscus  fuscus 

Distribution  of  Lasiurus  borealis  borealis 

Distribution  of  Lasiurus  cinereus  cinereus 

Distribution  of  Nyciiceius  humeralis  humeralis 

Distribution  of  Sylvilagus  floridanus  mallurus 

Distribution  of  Lepus  americanus  virginianus 

Distribution  of  Tamias  slriatus  fisheri  and  T.  s.  lysteri 

Distribution  of  Marmota  monax  monax 

Distribution  of  Sciurus  carolinensis  pennsylvanicus 

Distribution  of  Sciurus  niger  cinereus  and  S.  n.  vulpinus 

Distribution  of  Tamiasciurus  hudsonicus  loquax 

Distribution  of  Glaucomys  volans  volans 

Distribution  of  Oryzomys  palustris  palustris 

Distribution  of  Reithrodontomys  humulis  virginianus 

Distribution  of  Peromyscus  maniculatus  nubiterrae  and  P.  m. 


bairdii 


Distribution  of  Peromyscus  leucopus  noveboracensis 

Distribution  of  Neotoma  floridana  magister 

Distribution  of  Clethrionomys  gapperi  gapperi 

Distribution   of   Microtus   pennsylvanicus  pennsylvanicus  and 

M.    p.   nigrans 

Distribution  of  Pitymys  pinetorum  scalopsoides 

Distribution  of  Ondatra  zibethicus 

Distribution  of  Synaptomys  cooperi  stonei 

Distribution  of  Zapus  hudsonius  americanus 

Distribution  of  Napaeozapus  insignis  insignis 

Distribution  of  Canis  latrans 

Distribution  of  Vulpes  vulpes  fulva 

Distribution  of  Urocyon  cinereoargenteus  cinereoargenteus 

Distribution  of  Procyon  lotor  lotor 

Distribution  of  Mustela  erminea  cicognanii 

Distribution  of  Mustela  frenata  noveboracensis 

Distribution  of  Mustela  vison 

Distribution  of  Mephitis  mephitis  nigra 

Distribution  of  Spilogale  putorius  putorius 

Distribution  of  Lutra  canadensis 

Distribution  of  Lynx  rufus  rufus 


Page 

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159 
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165 


INTRODUCTION 

In  1950,  Marshall  C.  Gardner  (1950a,  1950b)  began  the  first  com- 
prehensive listing  of  Maryland  mammals,  but  he  completed  only  the 
sections  dealing  with  marsupials,  insectivores,  and  bats.  This  has  been 
the  only  statewide  study  of  Maryland  mammals  ever  undertaken,  al- 
though a  number  of  sectional  accounts  have  appeared,  including  those 
by  Goldman  and  Jackson  (1939),  Bures  (1948),  Hampe  (1939),  and 
Bailey  (1923).  In  addition,  Mansueti  (1950)  treated  in  detail  the 
extinct  and  vanishing  species  of  the  State. 

The  present  survey  originated  in  the  mid-1950's,  but  intensive  work 
on  it  was  not  begun  until  1962.  During  the  course  of  the  study,  field 
work  was  conducted  in  all  parts  of  the  State  except  the  Allegheny 
Mountain  section.  Specimens  collected  during  this  field  work,  and  the 
large  series  of  Maryland  mammal  specimens  available  in  the  national 
collections,  form  the  basis  for  the  present  survey.  In  the  "specimens 
examined"  sections  of  the  following  accounts,  the  specimens  are  in 
the  collections  housed  in  the  U.S.  National  Museum  unless  otherwise 
noted.  Abbreviations  used  in  the  text  for  other  institutions  from  which 
material  has  been  examined  are  K.U.  for  Museum  of  Natural  History, 
University  of  Kansas,  U.  Mich,  for  Museum  of  Zoology,  University  of 
Michigan,  and  U.  Md.  for  University  of  Maryland.  All  measurements 
given  in  the  accounts  are  in  millimeters. 

Several  species  are  included  in  the  body  of  the  text  for  which  there 
are  as  yet  no  valid  records  for  the  State.  These  have  been  indicated  by 
placing  the  common  names  in  parentheses.  They  are  included  because 
of  the  virtual  certainty  that  they  are  a  part  of  Maryland's  mammal 
fauna.  Of  one  of  these  species,  a  specimen  was  taken  in  West  Virginia 
only  a  few  feet  from  the  Maryland  state  line;  as  for  the  others,  Mary- 
land contains  abundant  suitable  habitat  and  they  are  known  to  occur 
both  north  and  south  of  the  State. 

Distribution  maps  have  been  prepared  for  all  land  species  except 
introduced  forms  and  certain  ones  that  have  been  restocked  or  are 
so  widespread  in  distribution  that  they  have  been  recorded  from  every 
county  in  the  State.  On  the  maps,  crosshatched  areas  represent  probable 
distribution,  shaded  symbols  indicate  specimens  examined,  unshaded 
symbols  indicate  published  records  or  other  reports  that  appear  to  be 
valid,  and  an  unshaded  symbol  with  a  dot  in  the  center  indicates  a  type 

1 


2  NORTH  AMERICAN  FAUNA  66 

locality.  When  more  than  one  species  or  subspecies  is  represented  on  a 
single  map,  circles  and  triangles  are  used  to  distinguish  them,  and  the 
crosshatchings  representing  their  probable  distributions  run  in  dif- 
ferent directions. 

I  want  to  express  my  thanks  to  Theodore  A.  Bookhout  and  Vagn 
Flyger  of  the  University  of  Maryland's  Natural  Resources  Institute 
for  contributing  a  number  of  Maryland  mammal  records.  I  also  want 
to  acknowledge  my  gratitude  to  the  late  Romeo  Mansueti  of  the 
Chesapeake  Biological  Laboratory,  Solomons,  Md.,  for  his  encourage- 
ment and  advice  on  a  number  of  distributional  problems. 

LOCATION  AND  AREA  OF 
MARYLAND 

Maryland  lies  between  the  parallels  of  35°  53'  and  39°  44'  north 
latitude  and  the  meridians  75°  4'  and  79°  29'  west  longitude.  It  is 
bounded  on  the  north  by  the  State  of  Pennsylvania  and  on  the  east  by 
the  State  of  Delaware  and  the  Atlantic  Ocean.  The  southern  boundary 
of  the  State  is  the  Potomac  River  which  separates  it  from  Virginia  and 
West  Virginia.  West  Virginia  also  borders  Maryland  on  the  west.  The 
District  of  Columbia  is  a  political  entity  on  the  Potomac,  between 
Prince  Georges  and  Montgomery  counties,  Maryland.  It  is  not  physio- 
graphically  distinct  from  Maryland  in  any  way,  and  herein  is  regarded 
as  a  part  of  Maryland. 

The  Maryland  Geological  Survey  lists  the  total  area  of  the  State  as 
12,300.21  square  miles,  of  which  2,437  square  miles  are  water.  Thus  the 
total  land  area  of  Maryland  is  9,863.21  square  miles,  making  the  State 
the  eighth  smallest  in  the  Union.  The  area  of  the  District  of  Columbia 
is  some  70  square  miles,  of  which  8  are  water. 

Maryland  extends  in  a  general  ESE-WNW  direction  for  about  320 
miles;  the  greatest  north-south  distance  is  approximately  150  miles. 
The  State  is  actually  a  narrow  cross  section  of  the  Coastal  Plain, 
the  Piedmont  Plateau,  and  the  Appalachian  ridges.  Elevations  pass 
gradually  from  sea  level  to  3,342  feet  on  Backbone  Mountain  in  Garrett 
County. 

Geologically,  Maryland  varies  greatly.  Formations  range  from  the 
most  ancient  granite  and  gneiss,  through  rocks  of  every  age  and  great 
mineralogical  diversity  down  to  the  coastal  deposits  of  Recent  times. 
Overlying  these  rock  formations  are  a  great  diversity  of  soils.  In  con- 
trast to  its  more  northern  neighbors,  Maryland  has  never  been 
glaciated. 


MAMMALS  OF  MARYLAND 


CECIL 


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Figure  1. — Map  of  Maryland  showing  the  23  counties,  Baltimore  City,  and  the 

District  of  Columbia. 


TEMPERATURE 

The  mean  annual  temperature  for  Maryland  is  53  to  54  degrees.  It 
varies  from  area  to  area,  the  greatest  difference  being  between  Worces- 
ter County  on  the  Eastern  Shore  and  Garrett  County  in  the  Alle- 
gheny Mountains:  according  to  Shreve  et  al.  (1910),  the  average  an- 
nual temperature  at  Sunnyside  in  Garrett  County  is  47.1  degrees, 
whereas  at  Pocomoke  City  in  Worcester  County  it  is  58,  a  difference 
of  11  degrees.  At  intermediate  points  the  average  annual  temperatures 
are  also  intermediate ;  the  differences  that  exist  are  due  to  such  factors 
as  elevation  and  proximity  to  the  ocean  and  Chesapeake  Bay.  The 
average  date  for  the  last  killing  frost  in  spring  in  western  Maryland 
is  the  first  week  in  May ;  farther  east  it  is  the  last  10  days  of  April. 
In  western  Maryland  the  average  time  for  the  first  killing  frost  in 
autumn  is  late  September ;  in  the  eastern  part  of  the  State  it  is  early 
November. 

AVERAGE  ANNUAL 
PRECIPITATION 

Precipitation  is  distributed  throughout  the  year,  but  with  a  some- 
what greater  amount  in  the  warmer  months  than  in  the  cold  season. 
The  heaviest  rainfall,  from  38  to  46  inches,  occurs  in  western  Maryland. 


4  NORTH  AMERICAN  FAUNA  66 

The  Coastal  Plain  receives  between  40  and  44  inches  each  year.  Calvert 
County  is  one  of  the  driest  areas  of  the  State  and  receives  only  about 
36  inches  yearly. 

EFFECTS  OF  CIVILIZATION 

Maryland,  like  most  other  eastern  States,  has  no  truly  virgin  areas. 
Even  in  the  remotest  regions  of  the  western  part  of  the  State,  logging 
has  been  conducted,  and  fields  and  pastures  range  well  up  onto  the  sides 
of  the  mountains.  Some  of  the  wildest  parts  of  the  State,  until  quite 
recently,  were  the  marshes  that  lined  both  the  eastern  and  the  western 
sides  of  Chesapeake  Bay  and  those  along  the  Atlantic  Ocean.  With  the 
expanding  populations  of  both  Washington  and  Baltimore  seeking 
areas  for  summer  recreation,  many  of  these  marshes  are  being  drained 
and  "improved"  for  human  habitation.  In  addition,  easy  access  is  now 
available  to  the  outer  barrier  beach  on  Assateague  Island.  The  subur- 
ban communities  of  all  the  larger  cities  of  the  State  are  spreading 
farther  and  farther  into  the  countryside  and  have  eliminated  some 
fine  woods,  swamps,  and  meadows.  This  is  particularly  true  of  Balti- 
more and  Washington,  the  suburbs  of  which  now  extend  25  miles  or 
more  into  the  surrounding  country.  As  a  result,  the  site  where  the  only 
specimen  of  the  rare  pigmy  shrew,  Microsorex  hoyi  loinnemana,  has 
ever  been  taken  in  Maryland  is  iiow  part  of  a  housing  project,  and  the 
southeasternmost  Coastal  Plain  locality  for  the  southern  bog  lemming, 
Synaptomys  cooperi^  has  met  the  same  fate.  Nevertheless,  a  number 
of  areas  remain  in  Maryland  which  are  relatively  isolated  and  which 
support  a  varied  and  abundant  mammal  fauna.  Some  species,  such  as 
the  white-tailed  deer  and  the  cottontail  rabbit,  have  actually  profited 
by  the  changes  man  has  brought  to  the  State. 

PRINCIPAL  BIOTIC  OR  NATURAL 
AREAS  IN  MARYLAND 

Maryland  lies  in  5  major  physiographic  provinces  (Fenneman, 
1938)  :  Coastal  Plain,  Piedmont,  Blue  Ridge,  Ridge  and  Valley,  and 
Appalachian  Plateaus. 

There  are  three  major  forest  regions  (as  described  by  Braun,  1950) 
in  Maryland  which  correspond  roughly  to  these  physiographic  prov- 
inces. They  are  the  Oak-Pine  Forest,  the  Oak-Chestnut  Forest,  and  the 
Mixed  Mesophytic  Forest.  Stewart  and  Robbins  (1958)  divide  these 
major  forest  regions  of  Maryland  into  biotic  or  natural  sections  that 
represent  areas  showing  floral  or  faunal  differences  of  a  secondary 
nature.  They  divide  the  Oak-Pine  Forest  region  into  an  Eastern  Shore 
section,  an  Upper  Chesapeake  Bay  section,  and  a  Western  Shore  sec- 


MAMMALS  OF  MARYLAND 


PHYSIOGRAPHIC  PROVINCES  OF  MARYLAND 

^^  Appalachian  Plateaus 

[    [  Ridge  and  Va 1  ley 

^^  Blue  Ridge 

^^a  Piedmont 

I  Coastal  Plain 


Figure  2. — Physiographic  provinces  of  Maryland. 


tion.  The  Oak-Chestnut  Forest  region  is  split  into  a  Piedmont  section 
and  a  Ridge  and  Valley  section,  while  the  Allegheny  Mountain  section 
comprises  the  Mixed  Mesophytic  Forest  region  in  Maryland. 

In  general,  mammal  distribution  in  Maryland  correlates  well  with 
these  natural  areas  or  sections,  and  reference  is  made  to  them  through- 
out the  text.  An  exception  is  that  of  the  Upper  Chesapeake  Bay  section 
(comprising  the  northern  portion  of  the  Eastern  Shore,  and  the  Coas- 
tal Plain  of  Baltimore  and  Harford  counties)  which  seems  to  be  too 
weakly  differentiated  as  a  biotic  area  from  adjacent  sections  to  have 
any  relevance  with  regard  to  mammal  distribution.  This  section  has 
been  deleted  herein,  the  northern  portion  of  the  Eastern  Shore  being 
assigned  to  the  Eastern  Shore  section,  and  the  Coastal  Plain  of  Balti- 
more and  Harford  counties  being  treated  as  part  of  the  Western  Shore 
section. 

The  following  is  primarily  a  condensation  of  Stewart  and  Robbins' 
description  of  Maryland's  biotic  sections. 

Eastern  Shore  Section 

The  upland  forests  of  this  section  are  composed  chiefly  of  loblolly 
pine  {Pinus  tcueda)  stands  and  oak-hickory  forests  or  a  mixture  of  the 
two.  Along  the  tidal  marshes,  loblolly  pine  is  found  generally  without 
deciduous  associates.  The  Eastern  Shore  section  is  poorly  drained  and 


NORTH  AMERICAN  FAUNA  66 


FiGUBE  3. — Biotic  sections  of  Maryland. 


there  are  many  upland  and  lowland  swamps  in  which  occur  sweetgum 
{Liquidamhar  styracvflua)  ^  blackgum  {Nyssa  slyvatica),  red  maple 
(Acer  ruhrum) ,  pin  oak  {Quercus  palustis),  and  American  holly  (Ilex 
opaca) .  Along  the  Pocomoke  River  there  are  many  plants  with  south- 
ern affinities  such  as  bald  cypress  (Taeodium  distichum) ,  red  bay 
(Persea  horbonia),  horse-sugar  {Symplocos  tinctoria),  water  oak 
{Quercus  nigra) ^  cross  vine  {Bignonia  capreolata)^  and  laurel-leaved 
greenbriar  {Smilax  laurifolia) .  In  the  northern  part  of  this  section  the 
upland  forests  are  almost  entirely  deciduous  and  of  the  oak-hickory 
type.  In  addition  there  are  such  habitats  as  barrier  beaches,  salt 
marshes,  and  brackish  marshes.  Elevation  is  under  100  feet,  and  the 
topography  is  flat. 

Western  Shore  Section 

The  upland  forests  of  the  Western  Shore  section  are  composed  of 
scrub  pine  {Pinus  virginiana)  stands,  oak-hickory  forests,  or  a  mix- 
ture of  the  two.  In  the  southern  part  loblolly  pine  is  common,  and  in 
the  sandy  soil  of  the  northern  part  pitch  pine  (Pinus  rigida)  fre- 
quently predominates.  Rich  moist  upland  forests  of  white  oak 
{Quercus  alba)  and  tulip  poplar  {Liriodendron  tulipifera)  occur  lo- 
cally throughout  the  section.  Small  seepage  areas  are  frequent  and 
usually  support  an  upland  swamp  forest  type  that  contains  a  well- 


MAMMALS  OF  MARYLAND  7 

developed  understory.  Flood-plain  forests  are  particularly  luxuriant 
in  the  Western  Shore  section.  Tidal  marshes  are  commonly  found 
around  the  numerous  estuaries.  Elevation  is  from  100  to  300  feet,  and 
the  topography  is  rolling. 

Piedmont  Section 

The  Piedmont  section  occupies  the  area  of  the  Piedmont  physiologi- 
cal province  (Fenneman,  1938)  and  a  small  part  of  the  Coastal  Plain 
known  as  Elk  Neck  in  Cecil  County.  The  forests  in  this  section  con- 
sist mostly  of  white  oak,  black  oak  {Quercus  velutina),  tulip  poplar, 
smoothbarked  hickories  (Carya  sp.),  and  flowering  dogwood  (Comus 
florida).  In  some  areas  chestnut  oak  {QiterciLS  prmus)  or  scarlet  oak 
{Quercus  coccinea)  is  common,  and  occasionally  stands  of  scrub  pine 
or  pitch  pine  are  found.  Beech  {Fagus  grandifolia)  is  often  encoun- 
tered on  ravine  slopes,  and  mixed  mesophytic  forest  communities  occur 
in  some  of  the  larger  valleys  with  steep  north  slopes.  These  communi- 
ties contain  a  mixture  of  central  and  northern  hardwoods  and  some- 
times hemlock  {Tsuga  canadensis).  Elevations  in  this  section  range 
between  300  and  800  feet,  and  the  topography  is  gently  rolling.  Much 
of  the  land  has  been  cleared  for  farming. 

Ridge  and  Valley  Section 

Chestnut  oak  is  the  common  tree  throughout  most  of  the  section, 
and  in  the  higher  elevations  it  is  often  found  in  nearly  pure  stands. 
In  dry  areas  and  on  slopes  with  southern  or  western  exposure  there  is 
scarlet  oak,  interspersed  with  occasional  stands  of  scrub  pine,  pitch 
pine,  or  Table  Mountain  pine  (Pinus  pungens) .  Most  of  the  ravines 
and  steep  northern  slopes  are  occupied  by  mixed  mesophytic  forest 
communities  in  which  the  common  species  are  hemlock,  white  pine 
{Pinus  strobus)^  beech,  sweet  birch  {Betula  lenta),  basswood  {Tilia 
americana),  sugar  maple  {Acer  saccharum),  tulip  poplar,  white  oak, 
and  northern  red  oak  {Quercus  rubra).  On  the  valley  floors,  white 
oak,  black  oak,  tulip  poplar,  and  flowering  dogwood  communities 
occur.  Groves  of  red  cedar  {Juniperus  virginiana)  are  found  in  the 
limestone  areas  of  the  Hagerstown  Valley.  The  section  consists  of  a 
series  of  parallel  ridges  that  range  up  to  2,000  feet  in  elevation. 

Allegheny  Mountain  Section 

This  area  is  a  high,  undulating  plateau,  averaging  about  2,500  feet 
above  sea  level.  Several  ridges,  some  500  feet  high,  cross  this  plateau 
diagonally  from  northeast  to  southwest.  The  highest  point  in  the 
State,  Backbone  Mountain  (3,342  feet),  is  in  this  section.  Hemlock 


8  NORTH  AMERICAN  FAUNA  66 

and  white  pine  are  occasionally  encountered  on  the  slopes  and  in  the 
valleys,  but  deciduous  trees  predominate.  These  include  sweet  birch, 
sugar  maple,  red  maple,  black  cherry  {Prunus  serotina),  basswood, 
beech,  shagbark  hickory  ( Carya  ovata) ,  white  oak,  and  northern  red 
oak.  On  higher  ridges,  northern  red  oak  and  red  maple  predominate, 
with  chestnut  oaks,  black  oak,  and  yellow  birch  {Betul<i  lutea)  inter- 
spersed. Scattered  red  spruce  {Picea  ruhens)  is  sometimes  also  found. 
In  valleys  above  2,400  feet,  there  are  some  relict  bogs  consisting  of 
sedge  meadows  and  bog  heaths  interspersed  with  patches  of  alder 
{Alnus  sp.),  great  laurel  {Rhododendron  maxim/am)^  red  spruce, 
hemlock,  yellow  birch,  and  red  maple. 

MARYLAND'S  MAMMALIAN  FAUNA 

These  biotic  sections  of  Maryland  are  not  suflSciently  differentiated 
to  support  widely  divergent  mammalian  populations.  Some  forms  are 
confined  to  one  or  two  sections  of  the  State,  but  in  general  the  mam- 
malian fauna  does  not  differ  greatly  from  section  to  section.  The 
average-fauna  formula  (Long,  1963)  discussed  below,  reveals  that 
the  most  significant  division  in  the  State  is  between  the  Piedmont  sec- 
tion and  the  Ridge  and  Valley  section.  The  most  diversified  mam- 
malian fauna  is  in  the  Allegheny  Mountain  section,  the  most  impov- 
erished in  the  Eastern  Shore  section. 

Long  (1963,  p.  139)  recommends  the  average-fauna  formula,  20 
(100)/(Ni-|-N2),  for  deriving  a  numerical  expression  of  the  faunal 
resemblance  of  one  area  to  another  (in  this  formula,  6^=  number  of 
kinds  common  to  both  faunas,  iVi= number  of  kinds  in  smaller  fauna, 
iV^2= number  of  kinds  in  larger  fauna).  Using  this  formula,  and  sub- 
stituting the  number  of  species  and  subspecies  for  each  section  of 
Maryland,  the  following  comparisons  were  obtained : 


Western 
Shore 

Piedmont 

Ridge  and 
Valley 

Allegheny 
Mountain 

Eastern  Shore 

90 

83 
92 

73 

77 
83 

62 

Western  Shore -_ 

67 

Piedmont _   _ 

68 

Ridge  and  Valley. 

?7 

These  percentages  show,  as  is  to  be  expected  in  an  area  of  this  small 
size,  that  the  marmnal  fauna  of  all  the  sections  of  Maryland  rather 
closely  resemble  one  another.  Naturally,  the  most  distant  sections  of 
the  State  geographically  and  ecologically,  the  Allegheny  Mountain 
and  the  Eastern  Shore,  differ  the  most  faunistically.  Nevertheless  75 
percent  of  the  species  and  subspecies  are  common  to  both  sections.  The 


MAMMALS  OF  MARYLAND  9 

closest  resemblance  between  two  sections  is  that  between  the  Western 
Shore  and  the  Piedmont.  Surprisingly,  the  two  Coastal  Plain  sections, 
the  Western  Shore  and  the  Eastern  Shore,  show  slightly  less  resem- 
blance to  each  other.  This  is  probably  due  to  the  isolating  effect  of 
the  Chesapeake  Bay  on  the  Eastern  Shore. 

The  percentages  show  clearly  that  the  Allegheny  Mountain  and 
Ridge  and  Valley  sections  have  close  faunal  resemblance,  and  that 
as  a  unit  they  stand  somewhat  apart  from  the  three  eastern  sections. 
Thus,  while  the  resemblance  ratio  of  the  Eastern  Shore  to  the  Western 
Shore  is  90  percent,  and  that  of  the  Western  Shore  to  the  Piedmont 
is  92  percent,  the  Piedmont  has  a  resemblance  to  the  neighboring  Ridge 
and  Valley  section  of  only  83  percent.  The  resemblance  of  the  Ridge 
and  Valley  to  its  neighboring  Allegheny  Mountain  section  returns 
to  87  percent,  indicating  that  these  two  sections  differ  to  some  extent 
from  the  three  eastern  sections,  which  in  turn  appear  to  form  a 
closely  allied  mammalian  fauna  unit.  Therefore,  the  most  strongly 
marked  division  with  regard  to  mammal  distribution  in  Maryland  is 
that  between  the  gently  rolling  Piedmont  of  Montgomery,  Howard, 
Baltimore,  Harford,  Carroll,  and  eastern  Frederick  Counties  and  the 
upland  Blue  Ridge  Mountains  (Ridge  and  Valley  section)  to  the  west 
in  Washington  and  western  Frederick  Counties. 

Taken  as  a  whole,  Maryland's  mammal  fauna  seems  to  be  more 
northern  than  southern  in  origin.  Only  a  few  distinctly  southern 
species  (represented  usually  by  small  numbers  of  individuals)  reach 
Maryland.  Some  of  these  are  Reithrodontomys  humulis,  Sorex  longi- 
rost?n.s,  and  SpUogale  putorius.  On  the  other  hand,  a  number  of 
distinctly  northern  species  reach  south  to  Maryland  {Sorex  cinereus, 
Mustela.  erminea,  Lejms  americanus,  Tamiasciurus  hudsonicus,  and 
a  number  of  others)  and  extend  even  farther  south,  particularly  in 
the  Appalachian  Mountains,  where  many  of  them  range  as  far  south 
as  North  Carolina  and  Tennessee. 

KEYS 

The  following  keys  employ  external  and  easily  observable  or  measur- 
able characters  when  possible.  In  a  few  instances  it  has  been  necessary 
to  resort  to  dental  characters  when  external  ones  were  not  sufficiently 
marked  to  separate  forms.  The  keys  are  designed  for  use  on  adult 
animals  only. 

Key  to  the  Orders  of  Maryland  Land  Mammals 

la.  Forelimbs  modified  as  wings Chiroptera  (bats) 

b.  Forelimbs  not  modified  as  wings 2 

2a.  Feet  provided  with  hoofs Artiodactyla  (even-toed  hoofed  mammals) 

b.  Feet  provided  with  claws ^ 


10  NORTH  AMERICAN  FAUNA  66 

3a.  Canine  teeth  absent;  incisors  chisel-like 4 

b.  Canine  teeth  present ;  incisors  not  chisel-like 5 

4o.  Upper  incisors  2-2 Lagomorpha  (rabbits,  hares,  etc.) 

b.  Upper  incisors  1-1 Rodentia  (gnawing  mammals) 

5a.  Canine  teeth  similar  in  appearance  to  other  teeth ;  eyes  inconspicuous 

Insectivora  (moles,  shrews,  etc.) 

b.  Canine  teeth  well  developed ;  eyes  not  rudimentary 6 

6a.  Tail  prehensile;  first  digit  on  fore  and  hind  limbs  opposable;  abdominal 

pouch  present  in  female Marsupialia  (pouched  mammals) 

b.  Tail  not  prehensile;  first  digit  not  opposable;  no  abdominal  pouch  pres- 
ent  Carnivora  (flesh  eating  mammals) 

Key  to  the  Order  Insectivora  in  Maryland 

la.  Forefeet  greatly  enlarged  and  adapted  for  digging 9 

b.  Forefeet  similar  in  size  to  hind  feet  and  not  adapted  for  digging 2 

2a.  Tail  short,  less  than  25  percent  of  total  length  of  animal 3 

b.  Tail  long,  more  than  30  percent  of  total  length  of  animal 4 

3a.  Coloration  grayish;  size  more  than  100  mm.;  32  teeth  in  mouth 

Blarina  brevicauda  (short-tailed  shrew) 
6.  Coloration  brownish;  size  small,  less  than  100  mm.;  30  teeth  in  mouth 

Cryptotis  parva  (least  shrew) 
4a.  Third  and  fifth  upper  unicuspid  teeth  minute  so  that  only  three  of  the 
five  upper  unicuspids  are  visible  when  skull  is  viewed  laterally 

Microsorex  hoyi  (pigmy  shrew) 
6.  Only  fifth  unicuspid  tooth  in  upper  jaw  minute  so  that  four  unicuspids 

are  visible  when  skull  is  viewed  laterally 5 

5a.  Total  length  145  mm.  or  more;  hind  feet  large  and  fringed  with  stiff 
hairs;  third  and  fourth  toes  of  hind  feet  thinly  webbed  for  about  half 

their  length Sorex  palustris  (water  shrew) 

6.  Total  length  135  mm.  or  less;  hind  feet  not  conspicuously  large  and  not 

fringed  with  stiff  hairs ;  no  webbing  on  any  toes 6 

6a.  Tail  more  than  55  mm.  in  length;  coloration  uniform  dark  gray  through- 
out    Sorex  dispar  (long-tailed  shrew) 

b.  Tail  less  than  55  mm.  in  total  length;  coloration  not  uniformly  dark 

gray 7 

7a.  Total  length  greater  than  110  mm Sorex  fumeus  (smoky  shrew) 

b.  Total  length  under  100  mm 8 

8a.  Coloration  reddish  brown Sorex  longirostris  (southeastern  shrew) 

b.  Coloration  dull  brown  or  grayish  brown Sorex  cinereus  (masked  shrew) 

9a.  Snout  fringed  with  fleshy  projections;  tail  long,  more  than  50  mm.  in 

length Condylura  cristata  (star-nosed  mole) 

b.  Snout  not  fringed  with  fleshy  projections;  tail  less  than  40  mm.  in 

length 10 

10a.  Tail  thin,  flesh-colored  and  scantily  haired 

Scalopus  aquaticus  (eastern  mole) 
b.  Tail  thick,  blackish  and  well  haired 

Parascalopif  breweri  (hairy-tailed  mole) 

Key  to  the  Order  Chiroptera  in  Maryland 

la.  Interfemoral  membrane  wholly  or  partially  furred  on  upper  surface 2 

b.  Interfemoral  membrane  not  furred  on  upper  surface 4 


MAMMALS  OF  MARYLAND  11 

2a.   Coloration  reddish-orange Lasiurus  borealis  (red  bat) 

b.  Coloration  brownish  to  black,  frosted  with  white 3 

da.  Total  length  greater  than  125  mm.;  interfemoral  membrane  wholly 
furred;  coloration  brownish,  heavily  frosted  with  white;  individual 

hairs  banded Lasiurus  cinereus  (hoary  bat) 

b.  Total  length  less  than  120mm.;  interfemoral  membrane  only  partially 
furred;  coloration  blackish,  lightly  frosted  with  white;  individual  hairs 

not  banded Lasionycteris  noctivagans  (silver-haired  bat) 

4a.  Ears  reaching  considerably  beyond  end  of  nose  when  laid  forward 5 

b.  Ears  not  reaching  noticeably  beyond  end  of  nose  when  laid  forward 6 

5o.  Ears  greatly  enlarged,  over  35  mm.  from  crown  in  length 

Plecotus  townsendii  (big-eared  bat) 

b.  Ears  not  noticeably  enlarged Myotis  keenii  (Keen  myotis) 

6a.  Over  100  mm.  in  total  length Eptesicus  fuscus  (big  brown  bat) 

b.  Under  100  mm.  in  total  length 7 

7a.  Under  85  mm.  in  total  length;  distinct  black  facial  mask 

Myotis  subulatus   (small-footed  myotis) 

b.  Over  85  mm.  in  total  length;  no  black  facial  mask 8 

8c.  Pale  golden  brown  in  coloration;  nose,  ears,  and  wings  reddish-brown 

Pipistrellus  subflavus  (eastern  pipistrelle) 

b.  Coloration  dark  brown ;  ears,  nose,  and  wings  nearly  black 9 

9a.  Fur  long,  thick,  and  shiny Myotis  lucifugus  (little  brown  bat) 

6.  Fur  short,  dull  and  sparse 10 

10a.  Coloration  dark  brown;  ears  thick  and  leathery 

Nycticeius  humeralis   (evening  bat) 
b.  Coloration  pinkish  brown;  ears  not  thick  and  leathery 

Myotis   sodalis    (Indiana    myotis) 

Key  to  the  Order  Lagomorpha  in  Maryland 

la.   Length  of  hind  foot  greater  than  115  mm  (as  much  as  150  mm.  in  some 
specimens) ;  coloration  white  in  winter 

Lepus   americanus    (showshoe  rabbit) 
b.   Length  of  hind  foot  less  than   115  mm.;  coloration  brownish  in  all 

seasons 2 

2a.  Black  on  forward  edge  of  ear  sharply  defined  from  brown  of  rest  of 
ear;  distinct  black  patch  betweep  ears 

Sylvilagus  transitionalis  (New  England  cottontail) 
b.  Black  on  forward   edge    of    ear   not  sharply  defined;  no  dark    patch 

between    ears Sylvilagus  floridanus    (eastern    cottontail) 

Key  to  the  Order  Rodentia  in  Maryland 

la.  Upper  incisors  with  longitudinal  grooves 2 

b.  Upper  incisors  withovit  longitudinal  grooves 5 

2a.  Tail  very  short,  equal  to  about  one-sixth  of  total  length 

Synaptomys  cooperi  (southern  bog  lemming) 

b.  Tail  longer  than  one-sixth  of  total  length 3 

3a.  Tail  less  than  one-half  of  total  length 

Reithrodontomys   humulis    (harvest   mouse) 
b.  Tail  greater  than  one-half  of  total  length 4 


12  NORTH  AMERICAN  FAUNA  66 

4a.  Coloration  of  sides  orange;  tail  often  tipped  with  white 

Napaeozapus    insignis    (woodland   jumping    mouse) 
h.  Coloration  of  sides  yellowish;  tail  never  tipped  with  white 

Zapus  hudsonius  (meadow  jumping  mouse) 

5a.  Tail  bushy 6 

b.  Tail  not  bushy 10 

6a.  Fore  and  hind  limbs  connected  by  a  loose  fold  of  skin ;  adapting  the  ani- 
mal for  gliding Glaucomys     volans     (southern     flying     squirrel) 

b.  Fore  and  hind  limbs  not  connected  by  a  loose  fold  of  skin 7 

7a.  Tail  less  than  one-quarter  of  the  total  length.  _  Marmota  monax  (woodchuck) 

b.  Tail  greater  than  one-third  of  the  total  length 8 

8a.  Coloration  reddish-brown  above;  under  325  mm.  in  total  length 

Tamiasciurus  hudsonicus  (red  squirrel) 

b.  Coloration  not  reddish-brown ;  over  325  mm.  in  total  length 9 

9a.  Coloration  of  upper  parts  gray,  darker  along  middle  of  back;  under 
550  mm.  in  total  length;  upper  premolars  2-2 

Sciurus   carolinensis    (gray   squirrel) 
b.  Coloration  of  upper  parts  variable-grayish,  reddish,  or  buflfy,  but  sides 
not  noticeably  paler  than  back;  over  550  mm.  in  total  length;  upper 

premolars    1-1 Sciurus    niger    (fox    squirrel) 

10a.  Coloration  on  back  reddish,  marked  with  several  longitudinal  black  and 

white  stripes Tamias  striatus  (eastern  chipmunk) 

6.  Back  not  striped 11 

11a.  Tail  flattened  horizontally,  paddle-like Castor  canadensis  (beaver) 

b.  Tail  not  horizontally  flattened 12 

12a.  Tail  compressed  laterally Ondatra  zibethicus  (muskrat) 

b.  Tail  not  compressed  laterally 13 

13a.  Total  length  over  325  mm 14 

6.  Total  length  less  than  275  mm 17 

14o.  Total  length  over  500  mm.;  aquatic  in  habits.-  Myocastor  coy  pus  (nutria) 

b.  Total  length  less  than  500  mm 15 

15a.  Tail  length  equal  to,  or  more  than,  half  total  length  of  animal 

Rattus  rattus  (black  rat) 

b.  Tail  length  less  than  half  total  length 16 

16a.  Tail  well  haired,  and  not  conspicuously  scaly 

Neotoma  floridana  (eastern  woodrat) 
b.  Tail  scantily  haired  and  noticeably  scaly.   Rattus  norvegicus  (Norway  rat) 
17a.  Tail  very  short,  equal  to  about  one-sixth  of  total  length 

Pitymys  pinetorum  (pine  vole) 

6.  Tail  longer  than  one-sixth  of  total  length IS 

18a.  Tail  only  moderately  short,  equal  to  about  one-third  of  the  total  length.  .     19 

b.  Tail  longer  than  one-third  of  total  length 20 

19a.  Back  marked  with  a  wide  band  of  dull  red  from  forehead  to  rump 

Clethrionomys  gapperi  (red-backed  vole) 
b.  Back  dark  brown  to  nearly  black..   Microtus  pennsylvanicus  (meadow  vole) 
20a.  Line  of  demarcation  between  coloration  of  back  and  abdomen  indistinct ; 

coloration  often  uniform  gray  throughout..   Mus  musculus  (house  mouse) 
b.  Sharp  line  of  demarcation  between  coloration  of  back  and  abdomen; 

abdomen  always  white 21 

21a.  Total   length    over    225    mm Oryzomys    palustris    (rice    rat) 

b.  Total  length  under  200  mm 22 


MAMMALS  OF  MARYLAND  13 

22a.  Coloration  on  back  chestnut  brown 

Peromyscus  leucopus  (white-footed  mouse) 
6.  Coloration  on  back  grayish  brown.  _  Peromyscus  maniculatus  (deer  mouse) 

Key  to  the  Order  Carnivora  in  Maryland 

la.  Coloration  black,  or  black  and  white 2 

h.  Coloration  not  black 4 

2o.  Size  large,  over  1,200  mm.  in  total  length;  tail  short  and  not  bushy 

Euarctos  americanus  (black  bear) 

b.  Under  800  mm.  in  total  length;  tail  long  and  bushy 3 

3a.  Upper  parts  marked  with  no  more  than  two  white  stripes 

Mephitis  mephitis  (striped  skunk) 
b.  Upper  parts  marked  with  four  or  more  white  stripes 

Spilogale  putorius  (spotted  skunk) 

4a.  Black  facial  mask ;  tail  ringed Procyon  lotor  (raccoon) 

b.  No  black  facial  mask ;  tail  not  ringed 5 

5a.  Total  length  under  700  mm 6 

b.  Total  length  over  900  mm 9 

6a.  Underparts  brown  except  for  white  spots  on  chin  and  throat 

Mustela  vison  (mink) 

b.  Underparts  whitish  or  yellowish 7 

7a.  No  black  tail  tip;  tail  less  than  one-quarter  of  total  length 

Mustela  nivalis  (least  weasel) 

b.  Black  tail  tip ;  tail  more  than  one-quarter  of  total  length 8 

8a.  Black  tail  tip  nearly  50  percent  of  tail  vertebrae  length 

Mustela  erminea  (ermine) 
b.  Black  tail  tip  40  percent  or  less  of  tail  vertebrae  length 

Mustela  frenata  (long-tailed  weasel) 
9a.  Claws  retractile;  pupils  of  eyes  elliptical;  tail  short,  less  than  165  mm 

Lynx  rufus  (bobcat) 
6.   Claws  not  retractile;  pupils  of  eyes  not  elliptical;  tail  long,  over  300 

mm 10 

10a.  Toes  of  fore  and  hind  feet  webbed;  tail  thick  and  heavy;  aquatic  in 

habits Lutra  canadensis  (otter) 

b.  Toes  not  webbed;  tail  not  thick  and  heavy;  not  aquatic  in  habits 11 

1  lo.  Coloration  reddish ;  tail  tip  white Vulpes  vulpes  (red  fox) 

b.   Coloration  grizzled  grayish;  no  white  tail  tip 12 

12a.  Total  length  over  1,050  mm Canis  latrans  (coyote) 

b.  Total  length  under  1,050  mm Urocyon  cinereoargenteus  (gray  fox) 

Key  to  the  Order  Artiodactyla  in  Maryland 

la.  Back  brownish,  or  reddish-olive  in  coloration,  speckled  with  indistinct 
white  blotches;  antlers  narrow  and  standing  erect  above  head;  small 

canine  teeth  in  upper  jaws Cervus  nippon  (Sika  deer) 

b.   Back  reddish-brown   (summer)   or  grayish  (winter)   in  coloration,  not 
speckled;  antlers  heavy,  and  curving  forward  over  head;  no  canine 
teeth  present  in  upper  jaws Odocoileus  virginianus  (Virginia  deer) 


336-897  O — 69- 


14  NORTH  AMERICAN  FAUNA  66 

ACCOUNTS  OF  SPECIES 

Order  MARSUPIALIA  (pouched  mammals) 

Family  DIDELPHIDAE  (opossums) 
OPOSSUM 

Didelphis  marsupialis  virginiana  Kerr 

Didelphis  virginicma  Kerr,  The  animal  kingdom  .  .  .,  p.  193,  1792. 

Type  locality. — Virginia. 

General  distribution. — In  the  eastern  United  States  from  Vermont,  New  York, 
central  Michigan,  Wisconsin,  and  Minnesota,  south  to  central  Georgia,  Alabama, 
Mississippi,  Louisiana,  and  Texas. 

Distribution  in  Maryland. — Occurs  abundantly  in  all  sections  of 
the  State. 

Distinguishing  characteristics.- — -Teeth  5/4,  1/1,  3/3,  4/4,  —  50;  tail 
naked  and  prehensile;  five  toes  on  each  foot,  the  first  on  each  hind 
foot  clawless  and  thumblike;  outer  hair  long  and  coarse,  underfur 
short  and  soft;  general  coloration  grizzled-grayish. 

Meam/reinents. — Three  adults  from  Cabin  John,  Montgomery 
County,  measure:  Total  length  780,  737,  795;  tail  vertebrae  298,  325, 
333;  hind  foot  70,  63,  70;  greatest  length  of  skull  117.7,  98.6,  111; 
zygomatic  breadth  63.5,  53.5,  54.7. 

Habitat  and  habits. — The  opossiun  prefers  densely  forested  areas. 
Llewellyn  and  Dale  (1964,  pp.  120-121)  found  that  at  the  Patuxent 
Research  Center,  near  Laurel,  Prince  Georges  County,  this  species  was 
primarily  an  animal  of  the  low,  dense  woodland,  favoring  sections 
near  water.  They  found  that  well-drained  upland  woods  were  less 
desirable,  and  the  open  cleared  or  cultivated  lands  seemed  to  be  of 
slight  value  for  the  opossum.  Nevertheless,  it  will  frequently  wander 
into  meadows  and  cultivated  fields  in  search  of  food.  The  prehensile  tail 
and  opposable  first  toe  on  the  hind  foot  make  this  animal  almost  as 
much  at  home  in  trees  as  on  the  ground. 

The  opossum  apparently  does  not  favor  the  pine  woods  and  salt 
marshes  along  the  Atlantic  coast.  One  specimen  was  taken  on  the 
Virginia  portion  of  Assateague  Island  in  the  early  1930's,  but  local 
residents  report  that  none  have  been  seen  there  in  a  number  of  years. 

The  species  is  abundant  in  the  Rock  Creek  Park  area  of  the  District 
of  Columbia,  often  wandering  into  nearby  regions  of  the  city  at  night, 
searching  for  food  and  sometimes  nimmaging  in  garbage  pails  in 
residential  areas  considerably  distant  from  the  wooded  areas.  One 
such  wanderer  recently  made  his  abode  in  the  backyard  of  a  row- 
house  near  the  center  of  the  city  where  he  remained  for  many  weeks, 


MAMMALS  OF  MABYLANI>  15 

visiting  a  nearby  porch  in  the  evenings  to  eat  the  pet  food  set  out  by 
the  owner  for  her  cat. 

The  opossum  is  a  marsupial,  distantly  related  to  such  animals  as  the 
kangaroo  and  the  koala  of  Australia.  It  gives  birth  to  live  young,  but 
the  young  are  bom  in  a  premature  condition  and  are  nursed  in  the 
pouch  or  marsupium  of  the  mother.  When  born,  they  are  naked  or 
grublike  in  appearance,  but  the  forelimbs  are  well  enough  developed 
to  be  used  for  crawling  into  the  pouoh.  Development  is  rapid  in  the 
pouch,  and  within  4  to  5  weeks  the  young  are  ready  to  leave  for  short 
periods.  Llewellyn  and  Dale  (1964,  pp.  118-121)  found  that  in  Mary- 
land the  opossum  begins  to  breed  in  early  February,  and  young  are 
found  in  the  pouch  until  August.  Hartman  (1952,  p.  73)  estimates  the 
gestation  period  as  slightly  under  13  days.  Evidently  two  litters  are 
produced  during  a  breeding  season,  but  the  first  litter  accounts  for 
the  majority  of  young.  Llewellyn  and  Dale  found  that  the  average 
number  of  young  for  57  litters  in  pouch  was  7.74. 

The  opossum  makes  its  home  in  almost  any  shelter  where  it  can  be 
dry  and  safe  from  enemies.  This  may  be  mider  sheds  or  buildings,  in 
brush  piles,  or  in  holes  in  trees.  In  its  eating  habits  the  opossum  is  as 
unselective  as  it  is  in  finding  a  shelter.  Hartman  (1952,  p.  62)  lists 
the  frequency  of  foods  taken  in  the  following  order:  insects,  fruits, 
invertebrates  (other  than  insects),  mammals,  reptiles,  grains,  birds, 
and  eggs.  It  also  eats  carrion. 

Specimens  examined. — Montgomery  County:  Bethesda,  2;  Boyds, 
1;  Cabin  John,  3;  Plummers  Island,  2;  no  exact  locality,  2.  Prince 
Georges  County:  Beltsville,  2;  Bladensburg,  1 ;  Branchville,  4;  Green- 
belt,  2 ;  Laurel,  36 ;  Patuxent  Research  Center,  2 ;  T.B.,  1.  District  of 
Columbia:  25. 

Other  records  and  reports. — Opossums  have  been  killed  in  every 
Maryland  county  (LeCompte,  1942). 

Remarks. — As  noted  by  Gardner  (1950,  p.  65),  Maryland  opossums 
are  indistinguishable  from  Virginia  topotypes  of  virginiana. 

Order  INSECTIVORA  (shrews,  moles,  etc.) 

Family  SORICIDAE  (shrews) 
MASKED  SHREW 
Sorex  cinereus  Kerr 

This  species  closely  resembles  the  southeastern  shrew  {Sorex  longi- 
rostris)  and  the  pigmy  shrew  [Microsorex  hoyi).  The  differences 
between  the  masked  shrew  and  these  other  species  are  discussed  under 
the  species  accounts  of  the  other  two. 

There  are  two  subspecies  of  Sorex  cinereus  in  Maryland.  These  are : 


16  NORTH  AMERICAN  FAUNA  66 

Sorex  cinereus  cinereus  Kerr 

Soreas  arcticus  cinereus  Kerr,  The  animal  kingdom  .  .  .,  p.  206,  1792. 

Type  locality. — Fort  Severn,  Ontario,  Canada. 

General  distribution. — This  is  a  wide-ranging  subspecies,  distributed  over 
much  of  the  northern  part  of  North  America.  In  the  eastern  United  States  it 
ranges  throughout  New  England,  New  Yorli,  and  western  Pennsylvania,  and 
south  in  the  Appalachian  Mountains  to  North  Carolina. 

Distribution  in  Maryland. — Kidge  and  Valley,  and  Allegheny  Moun- 
tain sections.  (See  fig.  4.) 

Distinguishing  characteristics. — Teeth  3/1,  1/1,  3/1,  3/3,  =  32;  third 
unicuspid  usually  larger  than,  or  equal  in  size  to,  fourth  unicuspid; 
size  very  small;  snout  elongated  and  pointed;  tail  long,  slightly  less 
than  half  the  total  length  of  the  animal;  ears  short  and  hidden  in  fur; 
coloration  in  winter  pelage  dark  brown  to  almost  black  on  upper  parts, 
lighter  brown  or  grayish  on  underparts ;  in  summer,  coloration  is  some- 
what lighter  and  more  brownish. 

Measurements. — An  adult  female  from  9  miles  east  of  Oldtown, 
Allegany  County,  measures :  Total  length  88 ;  tail  40 ;  hind  foot  1 1 ; 
ear  7;  condylobasal  length  of  skull  15.7;  cranial  breadth  7.4;  inter- 
orbital  breadth  2.3;  maxillary  breadth  3.9;  crown  length  of  upp^r 
toothrow  (exclusive  of  first  incisors)  5.4. 

Habitat  and  habits. — This  shrew  is  most  common  around  rocks  in 
moist  or  damp  coniferous  or  deciduous  woods.  Sometimes  it  lives  in 
grassy  bogs  and  swamps,  but  rarely  if  ever  in  dry  fields  or  woods 

The  nest  is  located  on  or  near  the  surface  of  the  ground,  in  a  cavity 
under  a  log,  rock,  or  other  object.  It  is  composed  mainly  of  leaves,  and 
in  shape  resembles  a  flattened  sphere  some  3  inches  in  diameter.  In 
its  ramblings  this  shrew  utilizes  surface  runways  that  it  constructs 
itself  and  subterranean  runways  that  have  been  dug  by  mice. 

The  masked  shrew  is  a  voracious  eater  and  consumes  a  wide  variety 
of  foods.  These  include  beetles,  moths,  caterpillars,  bugs,  flies,  crickets, 
spiders,  worms,  and  the  flesh  of  mice  and  other  shrews.  It  also  eats 
some  vegetable  matter  such  as  moss  and  seeds. 

Little  is  known  of  the  breeding  habits  of  the  masked  shrew.  The 
breeding  season  may  extend  from  March  to  September,  and  as  many 
as  three  litters  may  be  produced  in  a  single  season.  The  gestation  period 
is  probably  about  18  days,  and  from  4  to  10  young  are  produced  per 
litter,  the  usual  number  being  7.  The  male  stays  with  the  female  before 
and  after  pregnancy  and  during  the  early  development  of  the  young. 
A  young  shrew  is  able  to  shift  for  itself  within  20  to  25  days  after  its 
birth. 

The  shrew  is  physically  strong  for  its  size,  but  being  extremely  active 
it  seems  to  bum  itself  out  at  an  early  age.  Its  longevity  is  probably 
not  over  2  years  if  it  is  allowed  to  live  its  full  life  span. 


MAMMAI/S  OF  MARYLAND 


17 


Sorex  ainereus  cinereus 
▲  Specimens  examined 
A  Specimens  reported 

Sorex  ainereus  fontinalis 
0  Specimens  examined 
O  Specimens  reported 


Figure  4. — Distribution  of  Sorex  cinereus  fontinaUs  and  8.  c.  cinereus. 

Specimens  examined. — Allegany  County:  Mount  Savage,  1;  Old- 
town,  3  miles  E,  1 ;  Oldtown,  9  miles  E,  1.  Garrett  Gov/nty:  Bittinger,  2; 
Cunningham  Swamp,  4  (Coll.  U.  Md.) . 

Sorex  cinereus  fontinalis  Hollister 

Sorex  fontinalis  Hollister,  Proc.  U.S.  National  Museum,  40:  378, 
17  April  1911. 

Type  locality. — Cold  Spring  Swamp,  near  Beltsville,  Prince  Georges  County, 
Maryland. 

General  (Hstrihution. — Piedmont  and  Coastal  Plain  of  Pennsylvania,  Maryland, 
ani  northern  Virginia. 

Distribution  in  Maryland. — Piedmont,  Western  Shore,  and  Eastern 
Shore  sections. 

The  characters  of  this  race  seem  to  be  best  developed  in  the  lower 
Piedmont  section  near  Washington,  D.C.  (near  the  type  locality). 
Specimens  from  the  Coastal  Plain  sections  of  the  Eastern  Shore  and 
upper  Western  Shore  are  less  typical  and  apparently  represent  inter- 
grades  with  S.  c.  cinereus.,  which  is  distributed  to  the  northeast  in  New 
Jersey.  In  the  upper  Piedmont  the  subspecies  intergrades  with  S.  c. 
cinereus.  No  specimens  of  masked  shrew  have  been  taken  in  the 
southern  part  of  the  Western  Shore  section  (Calvert,  St.  Marys,  and 
Charles  Counties)  and  perhaps  the  species  does  not  range  this  far 
south  in  the  State. 


18  NORTH  AMERICAN  FAUNA  66 

Distinguishing  characteristics. — This  subspecies  is  very  similar  to 
S.  c.  cinsreus  and  differs  from  it  only  in  minor  details  which  are  most 
evident  on  the  skull.  Externally,  the  only  apparent  differences  are 
somewhat  smaller  size  and  shorter  tail.  The  skull  is  smaller,  with  a 
narrower  braincase  and  a  shorter,  relatively  wider  rostrum.  The  uni- 
cuspid  toothrow  is  shorter  than  in  S.  c.  cinereus^  and  the  teeth  in  the 
unicuspid  row  are  more  crowded. 

This  subspecies  of  masked  shrew  closely  resembles  the  southeastern 
shrew  {Sorex  longirostris) ,  which  in  the  eastern  United  States  reaches 
the  northern  limits  of  its  range  in  Maryland.  Differences  between  the 
two  are  discussed  under  the  species  account  for  Sorex  longirostris. 

Measurements. — External  measurements  of  eight  adults  from  the 
vicinity  of  Rockville,  Montgomery  County,  are  as  follows :  Total  length 
81.7  (76-89);  tail  vertebrae  33.7  (30-35);  hind  foot  10.6  (10-11). 
Cranial  measurements  of  five  adults  from  the  vicinity  of  Rockville 
are:  Condylobasal  length  14.9  (14.7-15.2)  ;  cranial  breadth  7.0  (6.7- 
7.1) ;  least  interorbital  breadth  2.7  (2.6-2.8) ;  maxillary  breadth  4.1 
(4.0^.2) ;  crown  length  of  upper  toothrow  (exclusive  of  first  incisors) 
5.5  (5.3-5.7). 

Habitat  and  habits. — Bures  (1948,  p.  62)  collected  14  masked  shrews 
(which  he  incorrectly  believed  to  be  Sorex  longirostris)  near  Lake 
Roland,  Baltimore  County.  He  says  that,  with  two  exceptions,  all  of 
these  shrews  were  taken  in  a  mixed  deciduous  woods  bordering  a  rail- 
road siding.  Of  the  two  exceptions,  one  was  trapped  in  a  dense  tangle 
of  sumac  and  honeysuckle  bordering  a  marsh,  and  the  other  in  similar 
habitat  along  a  small  stream  paralleling  Falls  Road.  He  states  that 
systematic  trapping  throughout  the  area  confirmed  his  opinion  that  this 
shrew  does  not  wander  far  from  deciduous  woods.  Hampe  ( 1939,  p.  5) , 
however,  trapped  this  shrew  in  the  Patapsco  State  Park  in  the  marshy 
pastures  near  Glenartney,  and  the  type  specimen  of  the  subspecies 
was  collected  in  a  cold  spring  swamp  in  Prince  Georges  County. 

This  shrew  apparently  does  not  occur  on  the  outer  barrier  beaches 
of  the  Atlantic  Coast.  Many  weeks  of  trapping  there  failed  to  produce 
a  single  specimen.  It  does  inhabit  the  adjacent  mainland,  and  the  skull 
of  one  was  found  in  an  owl  pellet  on  Mills  Island  in  Chincoteague  Bay, 
Worcester  County.  The  shrew  had  undoubtedly  been  captured  by  the 
owl  on  the  nearby  mainland. 

Regarding  the  nesting  habits  and  young  of  this  species,  Hampe 
(1936)  writes  that  he  examined  the  nest  of  one  which  was  under  a 
discarded  trash-filled  box  among  the  leaves  about  6  feet  from  the  road 
between  Glenartney  and  Vineyard,  Baltimore  County.  It  was  com- 
posed of  a  small  bundle  of  dried  and  broken  leaves  loosely  packed  in 
a  small  depression  in  the  ground.  It  was  fairly  dry,  but  the  surround- 
ing ground  was  very  damp.  This  nest  was  found  on  18  October  1936 


MAMMALS  OF  MARYLAND  19 

and  contained  six  blind  and  hairless  young.  At  the  time  of  this  dis- 
covery the  young  were  probably  a  week  old,  and  one  of  them  measured 
43  mm.  in  total  length  with  tail  and  hind  foot  measurements  of  12  and 
6  mm.  respectively.  The  nest  was  visited  again  in  about  2  weeks,  and 
the  young  had  developed  to  a  size  of  Y7  Tom.  in  total  length  with  tail 
and  hind  foot  measurements  of  33  and  10  mm.  They  were  well  furred 
and  quite  active.  When  the  nest  was  visited  for  the  final  time  on  8  No- 
vember, only  3  young  could  be  found,  and  they  quickly  scampered 
away  into  the  surrounding  brush.  The  mother  was  seen  in  the  nest  only 
when  it  wa^  first  investigated  on  18  October,  and  she  scurried  away 
very  rapidly  when  the  nest  was  opened. 

With  regard  to  feeding  and  breeding  habits  of  this  race  not  much 
is  known,  but  they  probably  are  similar  to  those  of  Sorex  c.  cinereus. 
As  with  cinereiis,  this  subspecies  appears  to  be  cyclical  as  far  as  abund- 
ance in  particular  areas  is  concerned ;  some  years  they  are  scarce,  in 
others  numerous.  An  example  of  how  abundant  these  shrews  may  be 
in  some  years  is  provided  by  Kyle  Barbehenn  who  collected  80  of  them 
near  Germantown,  Montgomery  County,  between  November  1958  and 
January  1959,  and  more  than  150  near  Rockville,  Montgomery  County, 
from  February  to  April  1959. 

Specimens  exammed. — Anne  Arwndel  Cownty:  Annapolis,  3  miles 
NW,  1;  Severn  Run,  1.  Baltimore  County:  Lake  Roland,  11;  Lock 
Raven,  5;  Pretty  Boy  Reservoir  (near  Middletown),  1.  Dorchester 
County:  Cambridge,  1.  Montgomery  County:  Ashton,  1;  Bethesda, 
1;  Cabin  John,  1;  Chevy  Chase,  1;  Germantown,  60;  Glen  Echo 
Heights,  1;  Great  Falls,  1;  Rockville  (near),  153;  Sandy  Spring,  1. 
Prince  Georges  County:  Beltsville,  1;  Bowie,  1;  Hollywood,  1;  Hy- 
attsville,  5 ;  Landover,  1 ;  Laurel,  3 ;  Patuxent  Wildlife  Research  Cen- 
ter, 3;  Tuxedo,  1.  Worcester  County:  Mills  Island,  1  (from  owl  pellet). 

Other  records  and  reports. — Kent  County:  Chestertown  (U.S.  Fish 
and  Wildlife  Service  files) .  Baltimore  Coumty :  Patapsco  State  Park 
(Hampe,  1936). 

Remarks. — This  shrew  was  for  many  years  considered  a  distinct  spe- 
cies. Poole  (1937,  p.  96),  however,  showed  that  in  Pennsylvania  there 
is  an  unbroken  gradation  between  this  form  and  Sorex  cinereus  and 
that  the  two  are  only  subspecifically  separable.  In  Maryland,  the  most 
typical  specimens  of  fontinalis  are  found  in  the  vicinity  of  the  type 
locality.  Farther  to  the  northwest,  near  Rockville  and  Germantown, 
Montgomery  County,  specimens,  although  still  referable  to  fontinalis^ 
are  somewhat  larger  than  typical  of  the  race,  and  are  approaching 
cinereus.  The  real  dividing  line  for  the  2  subspecies  in  Maryland  is 
that  between  the  Piedmont  and  the  Ridge  and  Valley  sections,  those 
to  the  west  being  referable  to  cinereus,  those  to  the  east  to  fontinalis. 
Specimens  from  north  of  Baltimore  and  from  the  Eastern  Shore  sec- 


20  NORTH  AMERICAN  FAUNA  66 

tion  also  appear  to  be  intergrading  with  jS.  c.  cmereus.  S.  c.  fontinalis 
appears  to  represent  the  end  of  a  cline  with  regard  to  small  size, 
shortening  of  the  rostrum,  crowding  of  the  unicuspid  toothrow,  and 
short  tail. 

Maryland  represents  the  southern  terminus  for  the  distribution  of 
the  species  Sorex  cinereits  east  of  the  Appalachian  Mountains. 

SOUTHEASTERN  SHREW 

Sorex  longirostris  longirostris  Bachman 

Sorex  longirostris  Bachman,  Journal  Acad.  Nat.  Science,  Philadel- 
phia, ser.  1,7(2):  370, 1837. 

Type  locality. — Hume  Plantations,  swamps  of  the  Santee  River  (=  Cat  Island, 
mouth  of  Santee  River) ,  South  Carolina. 

General  distribution. — The  southeastern  United  States  from  southern  Mary- 
land and  the  District  of  Columbia  to  central  Florida,  and  vrestvpard,  around 
the  southern  end  of  the  Appalachian  Mountains  to  Kentucky,  central  Indiana, 
and  Illinois. 

Distribution  i/n  Maryland. — The  southern  portion  of  the  Western 
Shore  section,  and  perhaps  extending  into  the  lower  Piedmont  section. 
Maryland  is  the  northernmost  limit  of  the  distribution  of  the  species 
in  the  eastern  United  States. 

Distinguishing  ch/wacteristics. — This  shrew  may  be  easily  confused 
with  Sorex  cinereus^  particularly  the  race  fontinalis.^  and  with  Micro- 
sorex  hoyi.  It  is  distinguished  from  Sorex  cinereus  by  the  following  : 
size  smaller;  tail  shorter;  coloration  more  reddish  in  winter  pelage; 
feet  smaller;  rostrum  short-er  and  blunter;  unicuspid  toothrow  more 
crowded;  and  a  greater  tendency  for  the  fourth  unicuspid  to  exceed 
the  third  in  size.  From  Microsorex  hm/i  it  differs  in  a  major  dental 
character.  In  Microsorex  the  third  upper  unicuspid  is  minute  and 
disk-like,  and  not  visible  when  the  jaw  is  seen  in  side  view.  The  fifth 
unicuspid  is  also  minute  and  not  visible  in  side  view,  so  that  only  3 
unicuspids  are  visible  laterally  in  the  upper  jaw,  the  first,  second,  and 
fourth.  In  Sorex  longirostris  (and  Sorex  eimereus)  4  or  5  unicuspids 
are  always  visible  when  the  skull  is  viewed  laterally.  In  addition, 
Sorex  longirostris  is  somewhat  larger,  more  reddish  in  coloration, 
and  has  a  longer  tail  than  Microsorex  hoyi. 

Measurements. — One  specimen  from  Chesapeake  Beach,  Calvert 
County,  has  the  following  cranial  measurements :  Condylobasal  length 
14.3;  cranial  breadth  6.6;  least  interorbital  breadth  2.9;  maxillary 
breadth  4.1;  crown  length  of  upper  toothrow  (exclusive  of  first  in- 
cisor) 5.1. 

Three  specimens  from  Raleigh,  N.C.,  average  82.6  mm.  in  total 
length  and  have  an  average  tail  lengtli  of  30.2  mm. 


MAMMALS  OF  MARYLAND 


21 


Sovex  longipostris    longirostris 
•  Specimens  examined 


FiGUBE  5. — Distribution  of  Sorex  longirostris  longirostris. 


Habitat  amd  habits. — Although  this  shrew  prefers  moist  situations 
such  as  bogs  and  damp  woods,  it  has  on  occasion  been  taken  on  com- 
paratively high  ground.  It  is  a  rare  species,  and  little  is  known  of  its 
habits,  although  they  probably  do  not  differ  much  from  those  of  B. 
cinereus.  An  interesting  sidelight  on  the  specimen  from  Chesapeake 
Beach,  Calvert  County,  is  a  notation  on  the  original  label  that  says 
"fell  over  cliffs  to  bayshore." 

Specimens  examJmed, — Anne  Arundel  County:  Shady  side,  1.  CaVvert 
Cov/nty:  Camp  Roosevelt,  2;  Chesapeake  Beach,  1.  Prince  Georges 
County:  Hall,  1.  District  of  Columbia :  1. 

Remarks. — It  is  interesting  to  note  that,  in  the  eastern  United  States 
at  least,  the  ranges  of  Sorex  cinereus  and  Sorex  longirostris  do  not  at 
present  seem  to  overlap  anywhere.  North  of  a  certain  line  (in  Mary- 
land this  line  lies  in  the  Western  Shore  section  between  Wasliington, 
D.C.,  and  Shadyside,  Anne  Arundel  County)  all  specimens  collected 
have  been  S.  cinereus.,  whereas  south  of  this  line  S.  longirostris  only 
has  been  taken.  There  does  not  appear,  however,  to  be  any  evidence  of 
intergradation  between  the  species.  Specimens  of  S.  longirostris  from 
Calvert  and  Anne  Armidel  Counties,  Md.,  are  just  as  typical  of  that 
species  as  are  those  from  farther  south  in  North  and  South  Carolina, 
whereas  specimens  from  Rockville,  only  a  few  miles  away,  are  clearly 
S.  cinereus.  That  the  two  are  distinct  species  is  further  demonstrated 


22  NORTH  AMERICAN  FAUNA  66 

by  the  fact  that  both  have  been  taken  in  the  same  field  in  central 
Indiana. 

In  all  probability  Sorex  ciner&us  will  eventually  be  found  to  be  a 
resident  of  the  southern  portion  of  the  Western  Shore  section,  and 
S.  longirostris  may  be  distributed  through  more  of  the  Piedmont  and 
northern  Western  Shore  section  than  is  currently  indicated. 

(WATER  SHREW) 

Sorex  palustris  punctulatus  Hooper 

Sorex  falustris  'punctulatus  Hooper,  Occas.  Papers  Mus.  Zool.  Univ. 
Mich.,  463 : 1, 15  September  1942. 

Type  locality. — West  Virginia,  Randolph  County,  6  miles  northwest  of  Durbin, 
Shavers  Fork  of  the  Cheat  River,  3,600  feet  elevation. 

General  distribution. — "Allegheny  Mountains  of  eastern  West  Virginia,  and 
probably  also  of  southwestern  Pennsylvania,  western  Maryland,  and  northwestern 
Virginia."  (Hooper,  l&i2,  p.  1). 

Distribution  in  Maryland. — Not  recorded  for  the  State,  but  undoubt- 
edly occurs  in  the  higher  elevations  of  the  Allegheny  Mountain  section. 

Distinguishing  characteristics. — Largest  of  all  the  eastern  long- 
tailed  shrews;  hind  feet  large,  and  with  a  fringe  of  stiff  hairs;  third 
and  fourth  hind  toes  joined  by  thin  web  at  the  base  for  slightly  more 
than  half  their  length;  grizzled  coloration  on  upper  parts,  and  pale 
gray  underparts  in  winter  pelage;  tail  markedly  bicolored.  Tooth 
formula  as  in  8orex  cinereus^  but  third  unicuspid  smaller  than  fourth. 
This  is  an  amphibious  species,  well  adapted  for  an  aquatic  life. 

Measurements. — Hooper  (1942)  gives  some  measurements  of  the 
type  and  two  paratypes  (from  Randolph  and  Preston  Counties, 
W.  Va.)  as  follows:  Total  length  152,  153,  155;  tail  64,  70,  71;  hind 

foot  19,  20,  20;  condylobasal  length  of  skull  21.1,  21.2, ,  cranial 

breadth  10.6,  10.3, ;  interorbital  breadth  3.9,  3.8,  3.9;  maxillary 

breadth  6.5,  6.4,  6.5 ;  maxillary  toothrow  7.9,  8.0,  8.1. 

Habitat  and  habits. — This  species  prefers  very  wet  areas  along  the 
borders  of  streams,  lakes,  and  ponds.  Often  it  is  found  in  marshes 
and  bogs,  and  in  beaver  and  muskrat  houses,  particularly  in  winter. 
It  favors  heavily  wooded  areas  and  is  rarely  found  in  marehes  that 
are  devoid  of  bushes  or  trees.  According  to  Hooper  (1942),  the  type 
specimen  of  the  subspecies  punHidatus  was  collected  under  a  log  at 
the  base  of  a  yellow  birch  sapling,  in  a  forest  of  spruce,  hemlock,  yel- 
low birch,  maple,  and  beech,  about  100  yards  from  Shavers  Fork,  the 
nearest  body  of  water.  The  paratypes  were  taken  at  the  edge  of  streams 
feeding  or  draining  spruce  swamps,  one  specimen  among  bracken, 
rhododendron,  and  hemlock,  the  other  among  sedges,  rushes,  willow, 
and  spruce.  There  are  many  areas  similar  to  this  in  Garret  County 


MAMMALS  OF  MARYLAND  23 

■which  the  water  shrew  may  inhabit,  and  one  of  the  specimens  men- 
tioned by  Hooper  was  taken  one  mile  south-southeast  of  Cranesville, 
Preston  County,  W.  Va.,  at  an  altitude  of  2,600  feet,  only  a  few  yards 
from  the  Maryland  State  line. 

This  shrew  does  not  hibernate  and  is  active  all  winter.  It  is  primarily 
nocturnal  in  habits,  but  occasionally  is  abroad  during  daylight  hours. 
It  is  well  adapted  to  an  aquatic  life  and  is  one  of  the  best  swimmers  of 
the  nonmarine  mammals.  It  can  swim,  dive,  float,  run  along  the  bottom 
of  a  pond  or  creek,  and  actually  run  upon  the  surface  of  the  water  for 
some  distance.  Jackson  (1961,  p.  38)  says  that  he  once  saw  a  water 
shrew  run  a  distance  of  more  than  5  feet  across  the  surface  of  a  pool. 
The  body  aad  head  of  the  animal  were  entirely  out  of  the  water,  the 
surface  tension  of  the  water  supporting  the  shrew,  and  at  each  step 
the  animal  took  there  appeared  to  be  a  little  globule  of  air  held  by 
the  hair  fringe  on  the  hind  feet. 

Conaway  (1952),  writing  of  the  western  subspecies  navigator^  says 
that  it  apparently  has  an  extensive  breeding  season  since  pregnant 
females  have  been  collected  in  March,  suckling  females  the  first  week 
in  June,  half  grown  young  early  in  July,  a  female  with  five  small 
embryos  on  August  2,  and  a  male  with  enlarged  testes  on  9  August. 
The  number  of  embryos  varies  from  4  to  8,  and  the  gestation  period 
is  probably  about  21  days.  These  shrews  do  not  live  long;  Conaway 
estimates  that  the  maximum  age  of  any  specimen  obtained  would  not 
be  in  excess  of  18  months. 

The  food  of  the  water  shrew  consists  largely  of  insect  matter,  chiefly 
beetles  and  their  larvae,  flies,  caddisflies,  and  mayflies.  Snails,  leeches, 
small  fish,  and  fish  eggs  are  also  consumed.  Vegetable  matter  probably 
supplies  only  a  small  part  of  the  diet. 

SMOKY  SHREW 
Sorex  fumeus  fumeus  Miller 

/Sorex  fimieus  Miller.  North  American  Fauna,  10:  50,  31  December 

1895. 

Type  locality. — Peterboro,  Madison  County,  N.Y. 

General  distribution. — Eastern  North  America,  from  southeastern  Ontario 
and  central  New  England  to  the  Smoky  Mountains  and  northern  Georgia.  It  has 
also  been  reported  from  central  Kentucky  (Barbour,  1951,  p.  102)  and  south- 
eastern Wisconsin  (Jackson.  1928,  p.  65). 

Distribution  in  Maryland. — Higher  elevations  (above  2,000  feet)  in 
the  Allegheny  Mountain  section ;  may  also  occur  at  higher  elevations 
in  the  Ridge  and  Valley  section.  It  is  not  a  common  species  in 
Maryland. 

Distinguishing  characteristics. — In  summer  pelage  resembles  Sorex 
cin^reus,  but  is  larger,  has  a  longer  tail,  bigger  feet,  and  somewhat 


24 


NORTH  AMERICAN  FAUNA  66 


Sorex  fumeus  fimeus 
0  Specimens  examined 
O  Specimens  reported 


Figure  6. — Distribution  of  Sorex  funieiis  fumeus. 


paler  coloration.  In  winter  pelage,  coloration  is  grayish,  and  this  shrew 
resembles  Sorex  dispar,  but  has  a  shorter  tail.  Tooth  formula  as  in 
Sorex  cinereus ;  third  unicuspid  larger  than  fourth. 

Measy/rerrhents. — Six  adults  from  Finzel,  Garrett  County,  6  miles 
north  of  Frostburg,  average  as  follows:  Total  length  110.8  (104—118) ; 
tail  44.5  (42-50) ;  hind  foot  13.2  (13-14) ;  condylobasal  length  of  skull 
(average  of  3)  17.9  (17.7-18.2)  ;  cranial  breadth  (average  of  4)  8.7 
(8.6-8.9) ;  least  interorbital  breadth  3.7  (3.6-3.9) ;  maxillary  breadth 
5.0  (4.8-5.3) ;  length  of  maxillary  toothrow  (average  of  5)  6.7 
(6.5-6.8). 

Habitat  and  habits. — The  smoky  shrew  is  essentially  a  northern  and 
mountain  species  and  reaches  its  greatest  abundance  in  the  cool  forested 
regions  of  New  England,  New  York,  and  Pennsylvania.  Most  of  Mary- 
land apparently  does  not  provide  suitable  habitat,  for  it  is  not  a  com- 
mon species  in  the  State.  It  prefers  damp  woods  and  bogs  at  the  higher 
altitudes,  where  it  lives  under  moss-covered  logs  and  rocks.  E.  A. 
Preble's  field  notes  report  that  the  specimens  collected  at  Finzel  were 
taken  in  a  hemlock  and  rhododendron  swamp,  and  those  at  Bittinger, 
Garrett  County,  deep  in  a  hemlock  forest. 

This  shrew  does  not  hibernate,  and  in  general  is  active  at  all  hours 
of  the  day  and  night.  Its  weak  feet  are  not  adapted  for  digging  bur- 
rows, and  it  occupies  those  made  by  larger  mammals  such  as  the  hairy- 
tailed  mole,  short-tailed  shrew,  red-backed  mouse,  and  pine  mouse.  The 


MAMMALS  OF  MARYLAND  25 

nests  are  located  at  various  places  in  these  tunnels,  a  favorite  being 
under  a  log  or  stump.  These  nests,  usually  made  of  shredded  leaves,  are 
roughly  spherical  in  shape  and  about  the  size  of  a  baseball.  They  gen- 
erally are  situated  some  4  to  19  inches  below  the  surface  of  the  ground. 

Breeding  in  this  species  may  begin  in  late  March  and  the  earlier 
litters  appear  in  early  May.  As  many  as  three  litters  may  be  produced 
each  season,  the  last  appearing  in  late  August.  The  gestation  period 
is  about  20  days,  and  the  young  number  from  3  to  10,  5  or  6  being 
the  most  common. 

Hamilton  (1940,  p.  480)  lists  the  foods  of  the  smoky  shrew  as  the 
following:  insects,  earthworms,  vegetables,  centipedes,  snails,  sala- 
manders, mammals,  sowbugs,  spiders,  and  birds. 

Hamilton  ( 1943,  p.  486)  believes  that  adults,  after  completing  their 
reproductive  duties,  die  of  old  age  when  14  to  17  months  of  age. 

Specimens  examined. — Allegany  County:  Mount  Savage,  4  (Coll. 
U.  Md.) .  Garrett  County:  Bittinger,  3 ;  Finzel,  6 ;  Swallow  Falls  State 
Forest,  3. 

Other  records  and  reports. — Garrett  County:  Cranesville  Swamp, 
one  mile  SE  (Coll.  U.  Mich.) ;  Sang  Run  (Coll.  Maryland  Nat.  Hist. 
Soc.). 

LONG-TAILED  SHREW 

Sorex  dispar  dispar  Batchelder 

Sorex  macrurus  Batchelder,  Proc.  Biol.  Soc.  Washington,  10:  133, 
8  December  1896.  Not  S.  macrourus  Lehmann,  1822. 

Sorex  dispar  Batchelder,  Proc.  Biol.  Soc.  Washington,  24 :  9Y,  15  May 
1911.  (A  renaming  of  S.  macrurus  Batchelder.) 

Type  locality. — Beede's  (sometimes  called  I^nne  Heights),  in  township  of 
Keene,  Essex  County,  N.Y. 

General  distribution. — Mountainous  regions  of  the  eastern  United  States,  from 
Maine  south  into  North  Carolina  and  Tennessee. 

Distribution  in  Maryland. — Allegheny  Mountain  section ;  may  occur 
at  higher  elevations  in  Ridge  and  Valley  section.  It  has  been  taken  in 
Maryland  only  at  Muddy  Creek  Falls,  in  Swallow  Falls  State  Forest, 
Garrett  County  (Mansueti  and  Flyger,  1952,  p.  250).  It  is  one  of  the 
rarest  shrews  in  Maryland. 

Distinguishing  characteristics. — Similar  to  Sorex  fumeus.,  but  with 
a  longer  tail,  somewhat  smaller  size,  and  a  uniform  slate-gray  colora- 
tion in  all  pelages.  Tooth  formula  as  in  Sorex  cinereu^,  with  third 
unicuspid  equal  to  fourth  in  size. 

Measurements. — External  measurements  of  the  type  as  given  in  the 
original  description  are :  Total  length  130 ;  tail  60 ;  hind  foot  15 ;  ear  10. 


26 


NORTH  AMERICAN  FAUNA  66 


Sorex  dispar  dispar 
O    Specimens  reported 


Figure  7. — Distribution  of  Sorex  dispar  dispar. 


Some  cranial  measurements  of  the  type  as  given  by  Jackson  (1928, 
p.  90)  are:  Condylobasal  length  of  skull  18.2;  cranial  breadth  8.1; 
interorbital  breadth  3.5 ;  maxillary  toothrow  6.1. 

Habitat  and  habits. — This  shrew  prefers  moist  rocky  areas  and  the 
crevices  between  boulders,  and  large  masses  of  rocks.  It  has  also  been 
taken  under  moss-covered  logs  in  damp  coniferous  forests.  Mansueti 
and  Flyger  (1952,  p.  250)  report  that  the  three  specimens  they  col- 
lected on  6  September  1950,  at  Muddy  Creek  Falls,  in  Swallow  Falls 
State  Forest,  Garrett  County,  at  an  altitude  of  2,200  feet,  were  taken 
in  snap  traps  placed  on  ledges  in  crevices  of  outcropping  sandstone  2 
or  3  feet  above  a  small  stream's  level  in  a  relatively  cool  moist  hemlock 
and  rhododendron  forest.  Charles  O.  Handley,  Jr.  (1956,  p.  435)  says 
that  the  Virginia  specimen  he  took  on  Big  Mountain,  Giles  County,  in 
September  of  1955  was  secured  in  a  trap  set  about  12  inches  below  the 
surface  in  a  patch  of  talus. 

Very  little  is  known  of  the  habits  of  this  species,  but  in  all  proba- 
bility it  differs  little  from  other  long-tailed  shrews.  Hamilton  (1943, 
p.  39)  says  that  G.  H.  H.  Tate  collected  a  female  with  2  embryos  in 
late  August  in  the  Adirondack  Mountains  of  New  York. 

Records  and  reports. — Garrett  County:  Swallow  Falls  State  Forest, 
at  Muddy  Creek  Falls  (Mansueti  and  Flyger,  1952). 


MAMMALS  OF  MARYLAND^ 


27 


PIGMY  SHREW 

Microsorex  hoyi  winnetnana  Preble 

Microsorex  winnemana  Preble,  Proc.  Biol.  Soc.  Washington,  23 :  101, 
24  June  1910. 

Type  locality. — Bank  of  Potomac  River  near  Stubblefield  Falls,  Fairfax 
County,  Va. 

General  distribution. — Maryland,  south  into  western  North  Carolina. 

Distribution  in  Mart/land. — May  occur  in  all  sections,  but  is  rare. 
It  has  been  taken  in  Maryland  only  at  Berwyn,  Prince  Georges 
County. 

Distinguishing  characteristics. — This  is  the  smallest  mammal  in 
North  America  and  possibly  the  smallest  in  the  world  with  respect  to 
weight.  Externally  it  resembles  Sorex  cinereus  and  Sorex  longirostris., 
but  is  smaller  and  darker  (less  reddish)  and  has  a  shorter  tail.  Al- 
though the  tooth  formula  is  the  same  as  that  of  the  genus  Sorex.^  there 
are  certain  peculiarities  in  the  upper  unicuspid  toothrow  which  dis- 
tinguish it.  The  third  upper  unicuspid  is  minute  and  disklike,  com- 
pressed anteroposteriorly  between  the  second  and  fourth  unicuspids, 
and  is  not  visible  when  the  jaw  is  viewed  laterally.  The  fifth  unicuspid 
is  minute  and  peglike,  and  is  also  not  visible  in  side  view,  so  that  only 
three  unicuspids  can  be  seen  in  the  side  view  of  the  upper  jaw  (first, 


Figure  8. — Distribution  of  Microsorex  hoyi  winnemana. 


28  NORTH  AMERICANi  FAUNA  66 

second,  and  fourth).  This  differs  from  the  genus  Sorex  in  which  four 
or  five  unicuspids  are  always  visible  when  the  skull  is  viewed  laterally. 

Measurements. — External  measurements  of  the  Berwyn  specimen  are 
as  follows :  Total  length  86 ;  tail  29 ;  hind  foot  9.5.  The  skull  of  this 
specimen  is  crushed,  but  some  cranial  measurements  of  the  type,  as 
given  by  Jackson  (1928,  p.  210)  are:  Condylobasal  length  of  skull 
13.0;  cranial  breadth  6.1 ;  interorbital  breadth  2.7 ;  maxillary  toothrow 
4.1. 

Habitat  and  habits. — These  rare  shrews  are  little  known.  The  type 
specimen  was  dislodged  from  the  decayed  interior  of  a  large  fallen 
log,  and  the  specimen  from  Berwyn  was  found  in  the  decayed  heart 
of  a  dead  chestnut  tree,  cut  from  a  dry  hillside  at  some  distance  from 
water. 

Specimens  examined. — Prvnce  Georges  Cov/nty:  Berwyn,  1. 

SHORT-TAILED  SHREW 

Blarina  brevicauda  kirtlandi  Bole  and  Moulthrop 

Blarina  brevicauda  kirtlandi  Bole  and  Moulthrop,  Sci.  Publ.  Cleve- 
land Mus.  Nat.  Hist.,  5:  99,  11  September  1942. 

Type  locality. — The  Holden  Arboretum,  Kirtland  Township,  Lake  County,  and 
Chardon  Township,  Geauga  County,  Ohio.  (The  county  line  bisects  the  type 
locality. ) 

General  distribution. — Ranges  from  northwestern  Michigan,  eastern  Wisconsin, 
and  Illinois,  east  throughout  most  of  Pennsylvania  to  central  New  Jersey  and 
southward  through  Delaware,  Maryland,  and  West  Virginia  to  southwestern 
Virginia. 

Distribution  in  Maryland. — Abundant  in  suitable  habitat  in  all 
sections  of  the  State. 

Distinguishing  characteristics. — A  large,  short -tailed,  slate-colored 
shrew,  with  a  shorter  blunter  muzzle  than  any  of  the  shrews  previously 
discussed.  The  tooth  formula  is  as  in  Sorex.,  with  the  fifth  unicuspid 
being  minute.  The  teeth  are  generally  darkly  tinged  with  reddish 
brown. 

Measurements. — Thirty-seven  adults  from  the  vicinity  of  Annapolis, 
Anne  Arundel  County,  average  as  follows:  Total  length  115.2  (107- 
122) ;  tail  23.3  (19-27) ;  hind  foot  14.4  (13-15).  Seventeen  adults  from 
the  vicinity  of  Annapolis  have  the  following  cranial  measurements : 
Condylobasal  length  21.9  (20.8-22.7);  mastoidal  breadth  12.1  (11.4- 
12.8) ;  interorbital  breadth  5.8  (5.3-6.1) ;  maxillary  breadth  7.7  (7.3- 
8.0) ;  unicuspid  toothrow  8.6  (7.9-8.9). 

Measurements  of  eight  adults  from  Cambridge,  Dorchester  County 
(Coll.  K.U.),  are:  Total  length  103.6  (101-107) ;  tail  vertebrae  23.1 
(20-25.5) ;  hind  foot  13.6  (13-14.5)  ;  condylobasal  length  of  skull  21.0 


MAMMALS  OF  MARYLAND 


29 


r                  r 

7- 

7,6- 

rV 

i 

1 

U///////// 

^8 

-39«- 
-38*- 

SCA  L  E 
O        lO      20      30MILES 

^ 

i 

-39"- 

Blanna  breviaauda  kirtlandi 
#    Specimens   examined 
0    Specimens    reported 

T                         T* 

1 

76* 

aoM 

Figure  9. — Distribution  of  Blarina  brevicauda  kirtlandi. 


(20.5-21.7) ;  mastoidal  breadth  11.3  (11.0-11.7) ;  interorbital  breadth 
5.4  (5.3-5.6) ;  maxillary  breadth  7.3  (7.1-7.6) ;  unicus,pid  toothrow  7.6 
(7.2-8.2). 

Habitat  and  habits. — This  is  one  of  the  most  abundant  mammals  in 
Maryland.  It  is  found  in  a  wide  variety  of  habitats,  but  is  most  numer- 
ous in  damp  woods  where  there  is  a  thick  understory.  It  is  also  en- 
countered in  meadows  and  old  fields,  but  not  on  the  Atlantic  barrier 
beaches  of  the  Delmarva  Peninsula,  where  many  weeks  of  trapping  on 
Assateague  Island  failed  to  uncover  a  single  specimen.  Elsewhere  in 
the  State,  this  shrew  vies  with  the  meadow  mouse  and  the  white- footed 
mouse  in  abundance,  but  does  appear  to  be  cyclical  as  regards  numbers, 
and  in  some  years  is  more  plentiful  than  in  others. 

The  short-tailed  shrew,  like  other  Maryland  shrews,  is  active  the 
year  around,  neither  hibernating  nor  migrating.  It  is  abroad  both 
during  daylight  hours  and  at  night.  It  is  quick  and  energetic  in  its 
actions,  and  appears  to  be  constantly  on  the  go  during  its  periods  of 
activity.  Its  runways  zigzag  in  all  directions  and  lie  on  the  surface  of 
the  ground  just  beneath  the  vegetation  or  litter.  In  these  runways,  the 
short-tailed  shrew  constructs  two  types  of  nests.  One  of  these  is  a 
small  resting  nest,  and  the  other  a  much  larger  breeding  nest.  The  lat- 
ter may  be  some  6  to  10  inches  long  and  averages  about  4  inches  in 
diameter.  The  nests  are  made  of  leaves,  shredded  grasses,  and  other 

336-897  0—69 3 


30  NORTH  AMERICAN;  FAUNA  66 

vegetable  fibers.  In  general,  these  nests  are  not  as  finely  made  as  most 
mouse  nests. 

The  breeding  season  for  this  species  extends  from  March  to  Sep- 
tember, and  usually  two  or  three  broods  of  young  are  reared  each 
season.  The  gestation  period  is  from  21  to  22  days,  and  between  3  and 
10  young  may  be  produced,  although  the  average  number  is  slightly 
below  7.  These  young  leave  the  nest  in  18  to  20  days,  and  by  the  time 
they  are  3  months  of  age  they  are  essentially  mature  animals.  This 
shrew  may  live  up  to  3  years,  but  the  life  span  is  usually  less  than  this, 
probably  not  more  than  18  or  20  months. 

This  species  has  a  voracious  appetite.  Hamilton  (1930,  p.  30)  found 
that  an  examination  of  244  intestinal  tracts  from  New  York  State 
Blarina  yielded  the  following  food  percentages :  Insects  47.8,  arachnids 
2,  millipedes  1.7,  vertebrates  4.1,  crustaceans  6.7,  mollusks  5.4,  annelids 
7.2,  centipedes  3.8,  plant  matter  11.4,  inorganic  matter  2.3,  and  un- 
determinable material  5.2.  Only  1.7  percent  of  the  stomachs  examined 
were  empty. 

The  bite  of  this  shrew  is  poisonous.  Pearson  (1942)  found  that  a 
poisonous  extract  could  be  prepared  from  the  submaxillary  salivary 
glands  of  this  species  and  that  a  toxic  material  is  also  present  in 
the  saliva  and  may  be  introduced  into  wounds  made  by  the  teeth,  but 
because  of  the  small  size  of  the  animal  its  bite  probably  would  have 
little  if  any  effect  on  man.  There  have  been  reports,  however,  of 
distress  following  the  bite  of  a  shrew.  Maynard  (1889)  says  that 
when  he  was  bitten  by  one  of  them  he  experienced  considerable  pain 
and  swelling  in  the  vicinity  of  the  wound  which  persisted  for  a  week 
or  longer.  Others  have  been  bitten  repeatedly  by  shrews  of  this  species 
and  have  experienced  no  after  effects  whatsoever  other  than  the  distress 
accompanying  the  actual  breaking  of  the  skin  by  the  sharp  teeth. 

These  shrews  appear  to  be  somewhat  more  gregarious  than  most  other 
species  of  shrews.  It  is  not  uncommon  to  capture  a  specimen  each  night 
for  4  or  5  consecutive  nights  in  a  trap  set  in  the  same  place,  indicating 
that  the  animals  are  using  the  same  runways  if  not  actually  associating 
with  each  other.  It  may  be  stated,  however,  that  in  general  this  shrew 
is  solitary  and  pugnacious  both  to  its  own  kind  and  to  any  other 
creature  it  may  encounter. 

Specimens  examined. — Allegany  County :  Frostburg,  1  (Coll.  Frost- 
burg  State  College);  Mount  Savage,  42;  Oldtown  (near),  7.  Arnrie 
Arvmdel  County :  Annapolis  (near),  40;  South  River  and  U.S.  Route 
50  (junction  of),  1.  Baltimore  City :  1.  Baltimore  County:  Dulaney 
Valley,  1 ;  Loch  Raven,  1.  Calvert  Cowity:  Breezy  Point,  2 ;  Chesapeake 
Beach,  1 ;  Cypress  Swamp  along  Battle  Creek,  2 ;  Hungerf ord  Creek, 
314  miles  N  of  Solomons,  1;  Marine  Training  Base,  %  mile  N  of 
Solomons,  13 ;  Plum  Point,  1 ;  Scientist  Cliffs,  2 ;  Solomons,  2.  Charles 


MAMMALS  OF  MARYLAND  31 

Cownty:  Benedict,  1 ;  Marshall  Hall,  1 ;  Newport,  7.  Dorchester  Coun- 
ty:  Cambridge,  15  (14  in  Coll.  K.U.).  Garrett  County:  Bittinger,  5; 
Cranberry  Swamp,  1 ;  Finzel,  13 ;  Grantsville,  5 ;  Mountain  Lake  Park, 
2;  Swallow  Falls  State  Forest,  2;  S wanton,  4;  "Wolf  Swamp,  2.  Mont- 
gomery Cownty:  Burnt  Mills,  2;  Cabin  John,  1;  Cropley,  2;  German- 
town,  1 ;  Kensington,  1  mile  N,  2 ;  Plummers  Island,  3 ;  Poolesville,  1 ; 
Kockville,  17 ;  Rockville,  2.3  miles  NE,  6 ;  Sandy  Spring,  6 ;  Seneca,  3 ; 
Sececa  Creek  at  Clopper  Road  (Route  117),  1;  Silver  Spring,  6; 
Takoma  Park,  1.  Prince  Georges  Cownty:  Northwest  Branch  Ana- 
costia  River,  1 ;  Hyattsville,  5 ;  Lanham,  1 ;  Laurel,  4 ;  Mitchellsville, 
1  mile  W.,  2 ;  Oxon  Hill,  12 ;  Prince  Georges  County  Sphagnum  Bog,  1. 
Worcester  Cownty :  Mills  Island,  2  (skulls  from  owl  pellets) ;  Snow 
Hill,  5  miles  NE,  1.  District  of  Columbia:  107. 

Other  records  and  reports. — Baltimore  Cownty:  Lake  Roland 
(Bures,  1948,  p.  62) ;  Towson  (Gentile,  1949,  p.  11) .  Frederick  Cownty: 
Locust  Grove  (Merriam,  1895,  p.  13).  Kent  County:  Chestertown 
(U.S.  Fish  and  Wildlife  Service  files).  Prince  Georges  County: 
Bladensburg  (Bailey,  1896,  p.  100). 

Remarhs. — This  species  is  in  need  of  revision  throughout  its  range. 
Pending  this,  only  tentative  conclusions  may  be  reached  regarding  the 
various  races  and  their  distribution.  At  present  it  appears  that  three 
subspecies  are  distributed  along  the  northeastern  coast  of  the  United 
States.  The  most  northerly  race,  talpoides^  ranges  throughout  most  of 
New  England,  New  York,  extreme  northern  Pennsylvania,  and  north- 
ern New  Jersey.  It  is  a  large  pale  race,  with  an  elevated  cranium  and 
a  long  slender  rostrum.  Distribtued  along  the  east  coast  to  the  south  of 
talfoides  is  kirtlandi  from  northeastern  Ohio,  ranging  throughout 
most  of  Pennsylvania,  central  and  southern  New  Jersey,  Delaware, 
Maryland,  and  West  Virginia  into  southwestern  Virginia.  It  is  some- 
what smaller  and  darker  than  talpoides  and  has  a  shorter,  broader 
rostrum.  Distributed  to  the  south  of  kirtlandi  is  the  very  small  dark 
southern  race  carolinensis.  Several  authorities  have  considered  the 
range  of  carolinensis  to  extend  north  to  Cambridge,  Dorchester  County, 
Md.  (Bole  and  Moulthrop,  1942,  p.  108;  Gardner,  1950a,  p.  67;  Jones 
and  Findley,  1954,  p.  210).  I  have  examined  a  number  of  specimens 
from  this  locality  (as  well  as  series  from  farther  south  on  the  Delmarva 
Peninsula)  and  consider  them  to  be  intergrades  between  carolinensis 
and  kirtlandi^  but  closer  to  kirtlandi  and  referable  to  that  race.  The 
intergrading  character  of  this  population  is  reflected  primarily  in 
smaller  size,  particularly  as  regards  external  measurements.  The  aver- 
age total  length  of  eight  specimens  from  Cambridge  is  103.6  mm.  as 
contrasted  with  97.4  mm.  for  eight  specimens  from  South  Carolina 
(near  the  type  locality  of  carolinensis)  and  116  for  the  type  specimen 


32  NORTH  AMERICAN  FAUNA  66 

of  kirtlaifidi  from  northeastern  Ohio.  Cranially,  eight  adults  from 
Cambridge  average  closer  in  size  to  kirtJundi  and  have  an  average  con- 
dylobasal  length  of  21.0  and  a  mastoidal  breadth  of  11.3,  contrasted 
with  an  average  condylobasal  length  of  18.4  and  mastoidal  breadth  of 

10.1  in  typical  carolinensis  (25  specimens  from  Raleigh,  N.C.)  and  21.0 
and  11.9  in  the  type  specimen  of  kirtlandi.  Apparently  the  entire  south- 
em  portion  of  the  Delmarva  Peninsula  is  an  area  of  intergradation  be- 
tween kirtlandi  and  carolinensis.  Specimens  I  have  examined  from 
near  Wattsville,  Accomack  County,  Va.,  and  Cape  Charles  at  the 
southern  tip  of  the  Delmarva  Peninsula  in  Northampton  County,  Va., 
although  .still  decidedly  referable  to  kirtlandi,  are  smaller  in  size  both 
externally  and  cranially  than  typical  kirtlandi  and  appear  to  be  ap- 
proaching carolinsnsis. 

LEAST  SHREW 

Cryptotis  parva  (Say) 

Sorex  jyarvus  Say,  in  Long,  Account  of  an  expedition  from  Pittsburg 
to  the  Rocky  Mountains,  .  .  .  1 :  163,  1823. 

Type  locality. — West  bank  of  Missouri  River,  near  Blair,  formerly  Engineer 
Cantonment,  Washington  County,  Nebr. 

General  distribution. — The  species  is  distributed  over  most  of  the  eastern  and 
midwestern  United  States,  from  central  New  York,  Michigan,  Wisconsin,  Min- 
nesota, and  South  Dakota,  south  to  Florida  in  the  east,  and  northeastern  Mexico 
in  the  west. 

Distribution  in  Maryland. — Occurs  in  all  sections  of  the  State. 

Distinguishing  characteristics. — Teeth  3/1,  1/1,  2/1,  3/1,  =  30;  small 
size;  brownish  coloration;  short  tail.  Most  closely  resembles  Blarina 
brevicauda  but  is  smaller,  more  brownish,  and  has  30  teeth  instead 
of  32.  It  may  be  distinguished  from  all  other  shrews  in  Maryland  by 
its  short  tail. 

Measurements. — Six  adults  from  3/4  mile  N  of  Solomons  Island, 
Calvert  County,  measury  as  follows:  Total  length  76.3  (74-80)  ;  tail 

15.2  (1^16) ;  hind  foot  10(10-11) ;  condylobasal  length  of  skull  15.2 
(15.0-15.6) ;  palatal  length  6.5  (6.4-6.9)  ;  cranial  breadth  7.7  (7.6- 
8.0) ;  interorbital  constriction  3.6  (3.5-3.7)  ;  maxillary  breadth  5.0 
(5.0-5.1)  ;  molar  toothrow  5.4  (5.2-5.6). 

Habitat  and  habits. — Most  commonly  found  in  dry  fallow  fields  and 
stubble  in  the  uplands,  and  in  the  marshes  in  the  coastal  areas.  This 
shrew  appears  to  be  abundant  in  some  places,  and  scarce  or  absent  in 
almost  identical  habitat  elsewhere.  Along  with  Microtus  pennsyl- 
vam-cus,  it  is  the  most  frequently  taken  small  mammal  on  Assateague 
Island,  where  it  occurs  everywhere  except  on  the  sparsely  vegetated 
beach  dunes.  Another  area  of  abundance  for  the  species  is  the  dry 
fallow  fields  of  southern  Maryland.  In  such  a  field,  three-fourth  mile 


MAMMALS  OF  MARYLAND 


33 


r 1 

79-                                                                  76* 
1                                                                         ' 

v 

76° 

r's 

w 

PW^« 

^8 

1 

^j 

SCALE 
O        lO      20      30MILES 

^m 

1 

^« 

-as"- 

w///^ 

// 

"^^-i^W/W/YM 

■iJ^r//y/Y 

J  i>  ji     v^yOjj^y^sJ 

Cryptotis  parua  parva 

^^^y/Z/Y' 

A  '^^'Z^Wa/A^ 

0    Specimens   examined 

iw//ll/V/4'> 

\^^^////j//y^ 

"^v/y^^vL/// 

^ 

^^^^/Avv/V// 

'VVTVyY/X^I 

O    Specimens    reported 

^cx^'^jwjy/ 

// 

fixS ,  ^^(y^/ff/// 

7//A/r///l 

^& 

i 

My^i^^ 

'^MyM- 

-36*- 

■^ 

\M. 

r's.                                          rk- 

T7' 

76" 

ao~ 

Figure  10. — Distribution  of  Cryptotis  parva  parva. 


N  of  Solomons,  Calvert  County,  this  shrew  was  taken  in  traps  as  often 
as  the  short-tailed  shrew  and  the  house  mouse. 

This  small  shrew  generally  follows  the  runways  of  larger  mice  and 
shrews,  but  it  also  constructs  runways  of  its  own.  In  soft  ground  it 
sometimes  uses  its  snout  to  push  dirt  away,  and  by  worming  its  way 
along  may  make  a  tunnel.  These  small  burrows  are  not  much  different 
from  those  made  by  certain  large  beetles  or  other  insects  and  are  diffi- 
cult to  identify.  The  nest  of  this  species  is  usually  placed  in  a  slight 
hollow  on  the  surface  of  the  ground,  or  under  a  rock  or  log.  Rarely 
is  it  located  beneath  the  ground  and  then  only  at  a  depth  of  4  or  5 
inches  or  less.  Sometimes  it  will  utilize  artificial  objects  such  as  tin 
cans  in  which  to  nest.  The  structure  of  the  nest  is  globular,  and  com- 
posed of  dry  grass  and  leaves. 

The  breeding  season  for  this  species  is  from  March  to  November,  and 
young,  born  early  in  the  spring,  usually  breed  within  the  year.  The 
gestation  period  is  about  16  days,  and  between  four  and  five  broods 
may  be  produced  during  a  season.  The  number  of  young  per  litter 
varies  from  three  to  nine,  with  the  usual  number  being  four  to  six. 

The  food  of  this  species,  like  that  of  other  shrews,  consists  primarily 
of  insects  and  other  animal  matter.  It  is  known  to  eat  beetles,  bugs, 
grasshoppers,  earthworms,  millipedes,  and  snails.  It  is  also  said  to  be 
fond  of  salamanders,  frogs,  and  broods  of  young  honeybees. 


34  NORTH  AMERICANi  FAUNA  66 

Unlike  most  other  shrews,  the  least  shrew  is  gregarious,  and  may 
be  said  to  be  almost  colonial  in  habits.  Jackson  (1961,  p.  58)  says  that 
often  when  a  log,  slab,  or  rock  is  overturned  four  to  eight  or  more  of 
these  little  shrews  may  be  found  living  together  underneath.  Maurice 
K.  Brady  of  Washington,  D.C.,  told  Jackson  that  in  Virginia  near 
Washington  in  1925  he  uncovered  a  nest  of  this  species  which  con- 
tained 25  Cryptotis^  all  in  a  pile. 

Specimens  examined. — Allegany  County:  Oldtown,  9  miles  E,  1. 
Anns  Arundel  County:  Annapolis  (vicinity),  2.  Baltimore  County: 
Lock  Raven  Reservoir,  1.  Calvert  County:  Solomons,  1;  Solomons, 
%  mile  N,  7.  Charles  County:  Newport,  1.  Dorchester  County :  Black- 
water  National  Wildlife  Refuge,  1.  Montgoinery  County :  Bethesda, 
1 ;  Kensington,  13 ;  Poolesville,  1 ;  Sandy  Spring,  19.  Prmce  Georges 
County:  Laurel,  6;  Oxon  Hill,  1;  Patuxent  Research  Center,  5.  Qusen 
Annes  County:  Parson  Island,  1.  Worcester  County:  Ocean  City,  4 
and  5  miles  S,  7;  Ocean  City,  15  miles  S,  1;  Chincoteague  Bay,  2. 
District  of  Columbia :  8. 

Other  records  and  reports. — Montgomery  County :  Seneca  (Kilham, 
1954,  p.  252). 

Remarks. — This  species  is  in  need  of  revision  over  its  entire  range. 
Until  this  revision  is  completed,  all  specimens  from  Marvland  are 
provisionally  referred  to  Cryptotis  parva  parva. 

Family  TALPIDAE  (moles) 

HAIRY-TAILED  MOLE 

Parascalops  breweri  (Bach  man) 

Scalops  breweri  Bachman,  Boston  Jour.  Nat.  Hist.,  4 :  32,  1842. 

Type  locality. — Martha's  Vineyard,  Massachusetts  (there  is  some  question, 
however,  whether  this  species  ever  occurred  on  Martha's  Vineyard  Island). 

General  distribution. — Northeastern  United  States  and  adjacent  Canada,  south 
in  the  Appalachians  to  western  North  Carolina. 

Distribution  in  Maryland. — Occurs  at  higher  elevations  in  the 
Allegheny  Mountain  and  Ridge  and  Valley  sections. 

Distinguishing  characteristics.— Teeth  3/3,  1/1,  4/4,  3/3,  =  44;  tail 
short  and  hairy;  coloration  dark  slate  to  black  dorsally,  slightly  paler 
below;  pelage  soft  and  thick,  but  somewhat  coarser  than  in  the  eastern 
mole  {Scalopus  aguaticus) ;  palms  enlarged  and  nearly  circular  in  out- 
line; toes  not  webbed. 

This  species  can  readily  be  distinguished  from  the  eastern  mole 
by  its  hairy  tail,  and  from  the  star-nosed  mole  (Condylura  cristata) 
by  the  absence  of  nasal  projections. 

Measurements. — Jackson  (1915 :  80)  gives  external  measurements  of 
eight  males  from  Magnetic  City,  N.C.,  as  follows :  Total  length  149.5 


MAMMALS  OF  MARYLANiD 


35 


SCALE 

o 

lo  20 

ao  MILES 

Parascalops 

hrewevi. 

• 

Specimen 

s  examined 

O 

Specimer 

s  reported 

Figure  11. — Distribution  of  Parascalops  ireweri. 


(139-152) ;  tail  vertebrae  30  (23-36) ;  hind  foot  19.5  (18-20).  He  gives 
some  measurements  of  the  skulls  of  10  adult  males  from  Magnetic 
City  as  follows:  Greatest  length  32.4  (31-33.8);  mastoidal  breadth 
14.5  (13.9-15) ;  interorbital  breadth  7.3  (7.1-7.5) ;  maxillary  toothrow 
9.9  (9.2-10.2) .  Females  average  smaller  than  males. 

A  male  (probably  immature)  from  Vale  Summit  Road,  between 
Clarysville  and  Vale  Summit,  Allegany  County,  has  the  following 
external  measurements:  total  length  136;  tail  22;  hind  foot  16.  This 
animal  weighed  35.7  grams. 

Habitat  and  habits. — In  Maryland  this  mole  is  found  only  at  high 
elevations  in  the  western  part  of  the  State,  where  it  lives  in  loose 
well-drained  light  soils.  It  may  be  found  in  pastureland,  as  well  as 
in  the  deep  woods,  but  is  seldom  encountered  in  damp  areas  or  in  clay 
soils.  Although  the  eastern  mole  {Scalojms  aquaticus)  also  occurs  in 
western  Maryland,  it  appears  to  be  ecologically  or  at  least  altitudin- 
ally  separated  from  the  hairy-tailed  mole.  The  eastern  mole  has  been 
taken  in  the  lowlands ;  the  hairy-tail  only  at  higher  elevations. 

This  species  makes  irregular  subsurface  runways  which  form  an 
elaborate  network.  In  the  winter  these  tunnels  are  deep  so  as  to  avoid 
the  freezing  temperatures  of  the  upper  layers  of  earth.  Nests  are  con- 
structed in  these  deep  burrows,  some  10  to  20  inches  below  the  surface 
of  the  ground.  These  are  made  of  dried  grasses  and  leaves,  and  are 
some  6  inches  in  circumference. 


36  NORTH  AMERICANi  FAUNA  66 

Mating  occurs  in  March  or  April,  and  four  to  five  young  are 
produced  in  late  April  or  May  after  a  gestation  period  of  probably  a 
month.  The  young  moles  develop  rapidly  and  are  able  to  shift  for 
themselves  within  a  month.  They  are  sexually  mature  and  able  to 
breed  the  following  spring. 

The  primary  foods  of  this  species  are  earthworms,  insects,  insect 
larvae,  and  other  arthropods.  They  are  very  voracious  eaters,  and 
Hamilton  (1943,  p.  27)  reports  that  a  captive  mole  of  this  species 
weighing  50  grams  consumed  66  grams  of  earthworms  and  insect 
larvae  within  a  24-hour  period. 

Specimens  examined. — Allegany  County:  Mount  Savage,  1.  (Coll. 
U.  Md.) ;  Vale  Summit  Road,  between  Clarysville  and  Vale  Summit, 
1  (Coll.  U.Md.). 

Other  records  and  re-ports. — Allegany  County:  Warrior  Mountain 
(U.S.  Fish  and  Wildlife  Service  files).  Garrett  County:  Grantsville, 
near  (Coll. U.Mich.). 

Remarks. — Two  specimens  of  this  species  from  Grantsville,  Garrett 
County,  collected  28-29  August  1949  by  J.  A.  King,  and  now  stored  in 
the  Museum  of  Zoology,  University  of  Michigan,  are  the  first  actually 
taken  in  this  State.  The  species,  however,  is  probably  not  as  rare  in 
western  Maryland  as  the  few  trapping  records  and  reports  would 
indicate. 

EASTERN  MOLE 
Scalopus  aquaticus  aquaticus  (Linnaeus) 

(Sorex)  aquaticus  Linnaeus,  Syst.  Nat.,  ed.  10,  1 :  53,  1758. 

Type  locality. — Philadelphia,  Pa.  ( Fixed  by  Jackson,  N.  Amer.  Fauna  38,  p.  33, 
30  September  1915). 

General  distrihution. — Eastern  United  States,  from  southern  New  England, 
and  New  York  State,  south  to  Virginia,  and  in  the  Appalachian  Mountains 
south  to  Tennessee,  North  Carolina,  and  South  Carolina. 

Distribution  in  Maryland. — Eastern  Shore,  Western  Shore,  and 
Piedmont  sections  and  at  lower  elevations  in  the  Ridge  and  Valley 
and  Allegheny  Mountain  sections.  Rare  or  absent  apparently  in  the 
Ridge  and  Valley,  and  Allegheny  Mountain  sections  at  elevations  over 
2,000  feet. 

Distinguishing  characteristics.— Teeth  3/2,  1/0,  3/3,  3/3,  =  36;  fore- 
feet broad  and  greatly  enlarged,  adapted  for  digging;  body  stout  and 
cyclindrical;  pelage  soft  and  velvety,  black  to  brownish  black  in 
coloration;  tail  short  and  naked;  eyes  and  ears  small  and  not  visible 
on  superficial  examination. 

Differs  from  the  hairy -tailed  mole  {Parascalops  hrewcri)  in  that  the 
tail  is  short  and  naked,  and  from  the  star-nosed  mole  {Corvdylura 
cristata)  in  that  the  snout  is  without  fleshy  projections. 


MAMMALS  OF  MARYLAISTD 


37 


79- 

1 

r 

77- 

7,fe« 

rV 

^ 

/m 

"^^^ 

WMM 

M 

-39°- 

SCALE 
O         lO      20 

30  MILES 

J  y /m/\^J/ //^i- 

8 

-33°- 

Scalopus  aquai 
•   Specimens 

icus  aquations 
examined 

^//T/jy//^ 

-3B-- 

O    Specimens 

reported 

^^^ 

Ci 

1 
79- 

1 

T* 

1 

76° 

aoM 

Figure  12. — Distribution  of  Scalopus  aquaticus  aquaticus. 


Measurements. — Jackson  (1915,  p.  34)  gives  external  measurements 
of  15  adult  males  from  Washington,  D.C.,  as  follows:  Total  length 
163.4  (154-175)  ;  tail  vertebrae  26.5  (22-29)  ;  hind  foot  19.8  (18-21). 

Cranial  measurements  for  21  adult  males  from  Washington  and 
vicinity  are:  Greatest  length  34.3  (33.2-35.6)  ;  mastoidal  breadth  17.7 
(17-18.3)  ;  interorbital  breadth  7.4  (7.2-7.8) ;  maxillary  toothrow  10.8 
(10.4-11.3) .  Females  average  smaller  than  males  in  size. 

Habitat  and  habits. — The  eastern  mole  normally  lives  in  sandy  soils 
and  light  loams  in  meadows,  pastures,  cultivated  fields,  gardens,  lawns, 
and  thin  woods.  Rocky  areas  and  swamps  are  generally  avoided  since 
they  are  barriers  to  the  mole's  burrowing  activity.  It  does,  however, 
prefer  moist  situations  to  dry  ones.  Very  sandy  regions,  such  as  the 
barrier  beaches  that  line  Maryland's  ocean  front,  are  apparently  un- 
favorable to  the  eastern  mole,  and  many  weeks  of  searching  for  their 
signs  near  Ocean  City,  Worcester  County,  and  on  Assateague  Island  to 
the  south  proved  fruitless.  Bures  (1948,  pp.  61-62),  found  moles  in  the 
Bare  Hills-Lake  Roland  area  of  Baltimore  County  to  be  restricted  to 
the  moist  or  wet  soil  bordering  the  Lake  and  along  the  two  streams 
that  empty  into  Jones'  Falls.  He  says  that  numerous  individuals  were 
observed  at  work  on  the  lawns  of  propei'ty  fronting  Falls  Road.  In  the 
Ridge  and  Valley  and  Allegheny  Mountain  sections,  there  is  evidence 
that  this  species  occurs  only  in  the  lowlands,  whereas  higher  up  on  the 


38  NORTH  AMERICAN  FAUNA  m 

mountains  it  is  replaced  by  the  hairy-tailed  mole.  In  Mason  County, 
W.  Va.,  McKeever  et  al,  (1952,  p.  25)  found  an  eastern  mole  inhabit- 
ing the  sandy  soil  of  the  Ohio  River  bottomland  and  a  hairy-tailed 
mole  in  the  nearby  forest-covered  hills.  This  distribution  occurs  in  the 
Appalachians  in  general,  including  the  Ridge  and  Valley  and  Alle- 
gheny Mountain  sections  of  Maryland. 

The  eastern  mole  does  not  hibernate,  but  is  active  the  year  round. 
It  constructs  a  series  of  burrows  just  beneath  the  surface  of  the  ground 
during  wet  weather  to  facilitate  the  capture  of  earthworms  which 
form  a  major  part  of  its  diet.  In  dry  and  cold  weather  this  species  digs 
deeper  permanent  burrows  some  10  or  more  inches  below  the  surface. 
Rarely  does  the  eastern  mole  emerge  from  its  subterranean  burrows 
and  prowl  about  above  ground.  A  nest  is  built  in  one  of  the  permanent 
burrows,  which  may  be  from  5  to  18  inches  down,  usually  under  the 
roots  of  shrubs  or  stumps.  It  is  most  often  made  from  grass  and  root- 
lets, but  occasionally  leaves  are  employed.  This  nest  is  placed  on  the 
bottom  of  a  flattened  ellipsoidal  enlargement  of  the  tunnel,  the  length 
of  which  is  about  8  inches  and  the  diameter  about  5. 

Mating  in  this  species  takes  place  in  March  and  continues  into  April. 
The  young  are  bom  in  the  latter  part  of  April  or  in  May.  The  gesta- 
tion period  is  about  45  days,  and  from  two  to  five  young  are  bom  each 
season.  By  the  time  a  young  mole  is  5  weeks  of  age  it  is  more  than  half 
the  size  of  the  mother. 

Eighty  percent  of  the  diet  of  the  eastern  mole  is  animal  matter,  con- 
sisting primarily  of  worms,  insects,  and  insect  larvae.  Some  of  the 
favorite  foods  are  beetles,  earthworms,  wireworms,  white  grubs,  spi- 
ders, centipedes,  millipedes,  slugs,  and  insect  and  mollusk  eggs.  Some 
of  the  plant  matter  consumed  are  corn,  potatoes,  grass,  tomatoes,  ap- 
ples and  occasionally  wheat  and  oats.  The  eastern  mole  is  a  voracious 
eater  and  in  24  hours  may  consume  a  quantity  of  food  equal  to  its 
weight. 

Moles  are  harmful  when  they  disfigure  lawns  and  provide  highways  in  gardens 
for  field  and  pine  mice.  Their  destruction  of  insects  places  them  in  a  more  favor- 
able light.  A  friend  once  told  me  that  these  moles  had  almost  eliminated  the 
larvae  of  Japanese  beetles  on  his  grounds.  Tunneling  activities  of  moles  aid  in 
the  formation  of  soil.  (Hamilton,  1943,  pp.  23-24) . 

Specimens  examined. — Allegany  County:  Cumberland,  3  (Coll.  U. 
Md.).  Anne  Ai^ndel  County:  Annapolis,  3  miles  NW,  1 ;  no  exact  lo- 
cality, 2.  Baltimore  City:  2.  Calvert  County:  Chesapeake  Beach,  1; 
Plum  Point,  1;  Solomons,  4  miles  N,  1.  Charles  County :  Newport,  3. 
Hoicard  County:  no  exact  locality,  1  (embryo  in  alcohol).  Montgom- 
ery County:  Cabin  John,  2;  Capitol  View,  1;  Chevy  Chase,  1;  Plum- 
mers  Island,  5 ;  Rockville,  2 ;  Seven  Locks,  1 ;  Silver  Spring,  4 ;  Wood- 
side,  4.  Prince  Georges  County :  Beltsville,  2 ;  Berwyn,  1 ;  Branch ville, 


MAMMALS  OF  MARYLAND  39 

4;  Brookland,  1 ;  Highland,  1 ;  Landover,  2 ;  Laurel,  13 ;  Mount  Rainier, 
1 ;  Patuxent  Research  Center,  1.  District  of  Columbia:  83. 

Other  records  and  reports. — Anne  Arundel  County:  Severna  Park 
(Cooper,  1953,  p.  79).  Baltimore  County:  Lake  Roland  (Bures,  1948, 
p.  61);  Patapsco  State  Park  (Hampe,  1939,  p.  5).  Montgomery 
County:  Forest  Glen  (Bailey,  1896,  p.  100) . 

STAR-NOSED  MOLE 
Condylura  cristata  cristata  (Linnaeus) 

{Sorex)  cristatus  Linnaeus,  Syst.  nat.,  ed.  10,  1 :  53,  1758. 

Type  locality. — Eastern  Pennsylvania. 

General  distribution. — Southeastern  Canada,  and  northeastern  United  States, 
south  to  central  Minnesota,  Wisconsin,  Indiana,  Ohio,  eastern  West  Virginia, 
and  northern  Virginia. 

Distribution  in  Maryland. — ^Locally  abundant  in  all  sections  of  the 
State  although  apparently  rare  or  absent  in  some  areas  with  suitable 
habitat. 

Distinguishing  characteristics. — Teeth  3/3,  1/1,  4/4,  3/3,  =  44;  body 
form  mole-like,  but  more  slender;  forefeet  broad  and  enlarged  for 
digging,  but  not  to  the  same  extent  as  in  SccUopus;  pelage  black  in 
coloration,  somewhat  harsher  in  texture  than  that  of  Scalopus;  tail 
long,  and  at  certain  times  of  the  year  enlarged.  The  most  distinctive 
feature  of  this  mole  is  the  snout,  which  is  fringed  with  22  pink  pro- 
jections, or  tentacles,  and  is  responsible  for  the  popular  name  of  the 
animal. 

Measurements. — Two  adults  from  the  District  of  Columbia  measure 
as  follows:  Total  length  183,  185;  tail  vertebrae  65,  66;  hind  foot  28, 
28;  greatest  length  of  skull  33.9,  33.4;  mastoidal  breadth  12.8,  12.8; 
interorbital  breadth  6.8,  6.7 ;  maxillary  toothrow  6.6,  6.3. 

Habitat  and  habits. — The  star-nosed  mole  prefers  damp  habitat  in 
meadows,  fields,  woods,  or  swamps,  but  is  sometimes  taken  in  the  leaf 
mold  of  dense  forests,  or  in  relatively  dry  fields  in  which  there  are 
a  few  damp  spots  from  which  its  tunnels  radiate.  Occasionally  it  is 
found  at  a  considerable  distance  from  any  water.  One  specimen  was 
captured  in  June  1958  in  the  lower  Eastern  Shore  section  near  Watts- 
ville,  Accomack  County,  Va.,  a  few  miles  from  the  Maryland  boundary. 
It  was  taken  in  a  museum  special  mouse  trap  set  in  a  surface  runway 
in  dry  meadow  at  least  a  fourth  of  a  mile  from  the  nearest  water. 
Generally,  however,  the  star- nosed  mole  will  be  encountered  in  very 
wet  situations,  and  its  tunnels  frequently  lead  directly  into  a  stream 
or  pool.  This  animal  is  an  efficient  swimmer,  using  its  broad  forefeet 
as  oars  and  its  tail  as  a  scull. 


40 


NORTH  AMERICAN  FAUNA  66 


Condylura  aristata  aristata 
%    Specimens  examined 
O  Specimens  reported 


Figure  13. — Distribution  of  Condylura  cristata  cristata. 


The  star-nosed  mole  is  less  fossorial  than  the  eastern  or  hairy- 
tailed  moles;  it  is  active  both  day  and  night,  summer  and  winter. 
It  often  uses  surface  runways,  and  sometimes  in  the  winter  it  will 
burrow  in  the  snow,  or  even  run  across  it.  The  tunnels  that  this  species 
digs  are  more  irregular  in  pattern  than  those  of  other  Maryland  moles. 
These  burrows  are  deep  in  places,  and  then  abruptly  rise  to  near  the 
surface.  Frequently  the  tunnels  enter  the  bank  of  a  stream  a  foot 
or  more  below  the  water  line.  The  nest  of  the  star-nosed  mole  is 
constructed  of  leaves  and  grass  and  is  located  in  a  flattened  spherical 
chamber  about  5  or  6  inches  in  diameter  and  some  4  or  5  inches  high. 
It  is  usually  placed  3  or  4  inches  below  the  surface  of  the  ground,  but 
may  be  as  much  as  10  inches  down.  It  is  always,  however,  above  the 
high  water  level. 

It  is  believed  that  star-nosed  moles  pair  in  the  autumn  and  remain 
together  until  the  young  are  born.  Breeding  occurs  in  the  spring,  and 
birth  is  from  April  to  June,  the  gestation  period  being  about  45  days. 
There  is  only  a  single  litter  per  year,  and  the  size  of  the  litter  varies 
from  three  to  seven,  six  being  the  usual  number.  The  young  mature 
rapidly  and  are  ready  to  leave  the  nest  within  about  a  month's  time. 
Star-nosed  moles  are  more  gregarious  than  other  eastern  moles,  and 
may  perhaps,  be  colonial,  although  colonies  are  probably  formed 
through  family  lineage. 


MAMMALS  OF  MARYLAND  41 

Star-nosed  moles  are  amphibious,  and  spend  a  good  deal  of  time  in 
water.  They  are  excellent  swimmers  and  divers,  and  a  large  portion 
of  their  food  consists  of  aquatic  insects  and  worms,  only  about  one 
fourth  of  the  diet  being  composed  of  terrestrial  forms. 

Specimens  examined. — Charles  County:  Marshall  Hall,  1.  Garrett 
County:  Cranesville  Swamp,  1.  Howard  County:  Ellicott  City,  1. 
Montgomery  County:  Brookeville,  1 ;  Burnt  Mills,  1 ;  Cabin  John,  1 ; 
Chevy  Chase,  1 ;  Chevy  Chase  Lake,  1 ;  Oakdale,  1 ;  Plummers  Island, 
1;  Potomac  P.O.,  1;  Sandy  Spring,  1;  Silver  Spring,  1;  Woodside, 
2.  Prince  Georges  County:  Beltsville,  1;  College  Park,  2;  Glenndale, 
1 ;  Lanham,  1 ;  Laurel,  2 ;  Patuxent  River  Marsh,  1 ;  no  exact  locality, 
1.  District  of  Columhia:  10. 

Other  records  and,  reports. — Prince  Georges  County:  Branch ville 
(U.S.  Fish  and  Wildlife  Service  files).  Washington  County:  Wil- 
liamsport  (Jackson,  1915,  p.  91) , 

Remarks. — Maryland  specimens  average  somewhat  smaller  in  size, 
both  externally  and  cranially  than  typical  C.  c.  cristata.,  and  are  tend- 
ing in  this  character  toward  the  smaller  southern  subspecies  C.  c. 
pa^rva. 

Order  CHIROPTERA  (bats) 

Family  VESPERTILIONIDAE  (vespertllionid  bats) 

LITTLE  BROWN  MYOTIS 

Myotis  lucifugus  lucifugus  (Le  Conte) 

y[espertilio].  lucifugus  Le  Conte,  in  McMurtrie,  The  animal  kingdom 
.  .  .  bytheBaronCuvier,vol.  l,App.,p.431, 1831. 

Type  locality. — Georgia;  probably  the  Le  Conte  plantation  near  Riceboro, 
Liberty  County. 

General  distribution. — Eastern  and  northern  North  American  from  Alaska 
and  Labrador  south  in  the  Appalachians  to  Georgia,  and  west  into  Arkansas. 

Distribution  in  Maryland. — Abundant  in  all  sections  of  the  State. 

Distinguishing  characteristics. — Teeth  2/3,  1/1,  3/3,  3/3,  =  38;  face 
covered  with  fur  except  for  lips  and  nostrils;  ears  moderately  long, 
not  extending  beyond  nostrils  when  laid  forward;  tragus  slender  and 
pcinted;  wing  membrane  between  humerus  and  knee  sparsely  furred; 
interfemoral  membrane  not  furred;  coloration  rich  brown,  almost 
bronze;  v^ung  animals  much  darker  in  coloration;  sagittal  crest 
usually  lacking  on  sk^oll, 

Measureinents. — Eight  adults  from  the  District  of  Columbia  have 
external  measurements  as  foUow^s:  Total  length  85.6  (80-95);  tail 
vertebrae  38.5  (36-42)  ;  hind  foot  8.9  (8.0-10.5).  Some  cranial  meas- 
urements of  seven  adults  from  Washington,  D.C.,  are  as  follows: 


42 


NORTH  AMERICAN  FAUNA  66 


7  9-                                                                  7  6' 

77* 

76° 

73 

-39=- 
-3B'- 

SCALE 
O         lO       20       30MILES 

JtUJiul ill 

i 

1  k 

76° 

7  7 

1 

Myotis   lucifugus   luaifugus 
•    Specimens   examined 
O    Specimens    reported 

1                                                      1 

79'                                                             78- 

1                                                1 

OOM 

Figure  14. — Distribution  of  Myotis  lucifugus  lucifugus. 


Greatest  len^h  14.0  (13.7-14.2);  zygomatic  breadth  8.4  (8.0-9.1); 
interorbital  breadth  4.0  (3.9^.2) ;  length  of  maxillary  toothrow  5.1 
(5.0-5.2). 

Habitat  and  habits. — This  species  occurs  almost  everywhere,  roost- 
ing in  the  attics  of  houses,  in  hollow  trees,  or  in  caves.  It  is  gregarious 
by  nature ;  in  the  attic  of  one  house  near  Seneca  Point,  Cecil  County, 
over  9,000  were  found  roosting  at  one  time. 

The  little  brown  myotis  hibernates  in  winter  and,  in  some  areas  at 
least,  is  migratory  in  habits,  traveling  "flyway"  routes  from  winter 
hibernating  quarters  to  summering  areas.  During  these  migrations 
they  may  travel  as  far  as  100  to  150  miles  or  more,  returning  by  similar 
routes  to  their  winter  quartera  The  migratory  patterns  of  Maryland's 
little  brown  myotis  have  not  been  studied,  but  the  files  of  the  Bat 
Banding  Office,  U.S.  Fish  and  Wildlife  Service,  contain  two  records 
of  movements  of  this  species  into  the  State.  In  both  instances,  the 
little  brown  myotis  were  banded  in  Hellhole  Cave,  Pendleton  County, 
W.  Va.,  in  March  1964  and  were  picked  up  in  the  vicinity  of  Deep 
Creek  Lake  in  Garrett  County  in  June  and  July  of  1964.  Perhaps 
some  of  Maryland's  Myotis  lucifugus  population  winters  in  caves  in 
West  Virginia  and  Virginia,  and  travels  north  to  forage  in  Maryland 
during  the  summer.  Others  that  winter  in  Maryland  may  venture 
further  north  into  Pennsylvania  in  the  summer  months. 


MAMMALS  OF  MARYLAND  48 

Mating  in  this  species  usually  occurs  in  the  autumn,  before  the  bats 
enter  hibernation.  Normally  the  spermatozoa  survive  in  the  uterus 
throughout  the  winter,  and  fertilization  occurs  the  following  spring. 
Copulation,  however,  may  occur  during  the  winter  or  in  the  spring. 
The  gestation  period  probably  is  about  80  days,  and  the  young  are 
bom  in  late  May  or  early  June.  Usually  only  a  single  offspring  com- 
prises a  litter,  but  occasionally  two  are  produced.  In  about  4  weeks 
after  their  birth,  the  young  are  flying  and  foraging  for  their  own 
food.  Sexual  maturity  is  achieved  at  about  8  months.  There  is  only 
one  litter  per  season. 

The  food  of  the  little  brown  myotis  appears  to  be  composed  entirely 
of  insects,  particularly  nocturnal  species  of  moths,  beetles,  and  bugs. 
It  has  a  voracious  appetite,  consuming  large  numbers  of  insects 
nightly. 

This  bat  is  long-lived;  there  are  records  of  banded  animals 
recovered  in  good  health  as  much  as  20  years  after  banding. 

Specimens  examined. — Cecil  County:  Seneca  Point,  1.  Garrett 
County :  Oakland,  1.  Montgomery  County :  Plmnmers  Island,  1.  Dis- 
trict of  Columbia :  29. 

Other  records  and  reports. — Baltimore  County:  Patapsco  State 
Park  (Bull.  Nat.  Hist.  Soc.  Maryland  10  (1),  p.  5,  1939).  Garrett 
County:  Deep  Creek  Lake  (banding  recovery  record).  Montgomery 
County:  Edwards  Ferry  (banding  recovery  record).  Washington 
County:  Round  Top  Mountain,  near  Hancock  (banding  record). 

Remarks. — This  bat  is  far  more  common  than  the  few  locality 
records  above  would  indicate.  It  is  probably  the  most  abimdant  bat 
in  Maryland. 

KEEN'S  MYOTIS 

Myotis  keenii  septentrionalis  (Trouessart) 

[Vespertilio    gryphu^]    var.    septentrionalis    Trouessart,    Catalogus 
mammalium  •  •  .  ,  fasc.  1,  p.  131,  1897. 

Type  locality. — Halifax,  Nova  Scotia,  Canada. 

General  distribution. — Eastern  North  America,  from  Newfoundland,  Nova 
Scotia,  Quebce,  and  Ontario,  south  to  northern  Florida  and  west  to  Manitoba, 
North  and  South  Dakota,  Nebraska,  Kansas,  and  Arkansas. 

Distribution  in  Maryland. — Occurs  in  all  sections  of  the  State,  and 
is  common. 

Distinguishing  characteristics. — This  bat  is  similar  in  size  and  color 
to  the  little  brown  myotis  {Myotis  lu^ifugus) ,  but  may  be  distinguished 
from  that  species  by  its  long  ears,  which  extend  some  4  to  5  millimeters 
beyond  the  tip  of  the  nose  when  laid  forward.  The  skull  is  narrower  in 
proportion  to  its  length  than  that  of  the  little  brown  myotis. 


44 


NORTH  AMERICAN  FAUNA  66 


MijOtis  keenii  septentrionalis 
0    Specimens  examined 
O  Specimens  reported 


Figure  15. — Distribution  of  Myotis  keemi  septentrionaUs. 


Measurements. — External  measurements  of  three  adults  from 
Plununers  Island,  Montgomery  County,  are  as  follows:  Total  length 
81,  87,  75 ;  tail  vertebrae  38,  35,  35 ;  hind  foot  9,  9,  10.  Some  cranial 
measurements  of  four  adults  from  Plummers  Island  are :  Greatest 
length  14.5  (14.4r-14.7) ;  zygomatic  breadth  8.9  (8.8-9.0)  ;  interor- 
bital  breadth  3.6  (3.6-3.7)  ;  length  of  maxillary  toothrow  5.9  (5.7-6.0). 

Habitat  and  habits. — This  species  roosts  in  small  colonies  in  caves, 
and  under  loose  bark  on  trees.  Frequently  it  is  found  in  association 
with  the  little  brown  myotis,  from  which  it  differs  little  in  habitat 
selection  or  habits,  except  that  it  seems  to  be  more  solitary.  Mansueti 
(1941,  pp.  56-57)  found  one  sleeping  under  the  bark  of  a  dead  stand- 
ing tree  near  Arbutus,  Baltimore  County.  When  he  peeled  the  bark 
away,  the  bat  flew  to  a  nearby  tree  and  crawled  up  under  some  loose 
bark  on  it.  This  species  is  more  abundant  than  the  few  Maryland 
records  indicate. 

Specimens  examined. — Baltimore  County:  Bare  Hills,  1.  Mont- 
gomery County:  Cabin  John  Bridge,  1;  Plummers  Island,  5.  Prince 
Georges  County:  Muirkirk,  1.  District  of  Colwmbia:  4. 

Other  records  and  reports. — Baltimore  County:  Arbutus  (Man- 
sueti, 1941);  Lake  Koland  (Bures,  1948:  63).  Montgomery  County: 
Forest  Glen  (Miller,  1897:  76).  Washington  County:  Kound  Top 
Mountain,  near  Hancock  (bat  banding  record,  U.S.  Fish  and  Wildlife 
Service) . 


MAMMALS  OF  MARYLAND 


45 


INDIANA  MYOTIS 

My  Otis  sodalis  Miller  and  G.  M.  Allen 

Myotis  sodalis  Miller  and  G.  M.  Allen,  Bull.  U.S.  Nat.  Mus.,  144: 
130, 25  May  1928. 

Type  locality. — Wyandotte  Cave,  Crawford  County,  Indiana. 

General  distribution. — Eastern  United  States  from  central  New  England  west 
to  Wisconsin,  Missouri,  and  Arkansas,  south  into  northern  Florida.  It  occurs 
on  the  Atlantic  Coastal  Plain,  however,  only  in  the  New  England  area. 

Distribution  in  Maryland. — Apparently  very  rare  in  the  State.  Its 
distribution  is  probably  limited  to  limestone  caves  in  the  Ridge  and 
Valley  and  Allegheny  Mountain  sections. 

Distinguishing  characteristics. — Resembles  Myotis  hicifugus.^  but 
differs  in  coloration,  the  fur  being  a  dull  grayish  chestnut  rather 
than  bronze,  with  the  basal  portion  of  the  hairs  of  the  back  dull  lead 
colored;  coloration  of  underparts  pinkish  to  cinnamon;  hind  feet 
smaller  and  more  delicate  than  in  M.  lucifugus',  slight,  but  well-de- 
fined sagittal  crest  usually  present  on  skull. 

Measurements. — Two  adults  from  the  type  locality  in  Indiana  have 
measurements  as  follows:  Total  length  86,  87;  tail  vertebrae  35,  38; 
hind  foot  9,  9;  greatest  length  of  skull  14.1,  13.9;  zygomatic  breadth 
8.7,  8.3;  interorbital  breadth  3.8,  3.7;  length  of  maxillary  toothrow 
5.5,  5.3. 


Myotis  sodalis 

#  Specimens  examtn 
O  Specimens  report 


Figure  16. — Distribution  of  Myotis  sodalis. 
336-897  0—69 4 


46  NORTH  AMERICAN  FAUNA  66 

The  skull  of  an  adult  from  Oakland,  Garrett  County,  measures: 
Greatest  length  13.7;  zygomatic  breadth  8.1;  interorbital  breadth 
3.7 ;  length  of  maxillary  toothrow  5.0. 

Habitat  and  habits. — This  bat  roosts  almost  exclusively  in  lime- 
stone caves,  preferring  those  in  which  there  are  considerable  bodies 
of  water.  It  forms  large  colonies  and  is  often  found  in  association 
with  M.  lucifugus.  It  is  known  from  only  2  localities  in  Maryland. 

Hall  (1962)  has  thoroughly  studied  the  life  histoiy  of  this  bat.  He 
found  that  at  Blackball  Mine,  La  Salle  County,  111.,  the  earliest  date 
for  entrance  into  hibernation  was  14  September.  The  major  buildup 
of  the  hibernating  colony  was  during  October  and  the  first  part  of 
November.  The  hibernating  colony  starts  diminishing  in  early  April, 
and  by  the  first  week  of  June  no  sodalis  are  in  hibernation.  He  esti- 
mates that  the  average  hibernation  period  for  this  species  would  be 
from  15  October  to  20  April,  or  187  days.  He  found  that  large  num- 
bers of  Indiana  myotis  accumulate  in  a  few  caves  to  hibernate,  and 
that  for  five  consecutive  winters  the  species  was  found  in  the  same 
seven  caves  and  in  no  others  in  Edmondson  County,  Kentucky.  This 
species  also  occupies  caves  during  the  nonhibernating  summer  months, 
and  may  be  considered  a  true  cave  species. 

As  far  as  movements  and  migrations  are  concerned,  Hall  says  that 
the  same  individual  may  be  present  in  one  area  winter  and  summer 
whereas  others  may  move  as  much  as  250  miles  between  seasons.  He 
says  that  the  few  band  recoveries  indicate  that  certain  movement 
areas  exist  for  certain  populations.  For  instance,  he  found  that  one 
such  population  range  includes  Kentucky,  Indiana,  Illinois,  and  south- 
ern Ohio,  and  that  no  movement  takes  place  between  this  area  and 
the  Ozark  area  of  Arkansas  and  Missouri. 

Little  is  known  regarding  the  feeding  and  breeding  habits  of  M. 
sodalis.,  but  probably  they  are  quite  similar  to  those  of  M.  lucifugus. 
Like  that  species,  M.  sodalis  is  long-lived.  One  specimen  banded  in 
Carter  County,  Ky.,  on  12  March  1950,  was  recovered  in  good  health 
14  years  later  on  8  January  1964,  in  the  same  cave. 

SpecimeTis  examined. — Garrett  County:  Near  Oakland,  1. 

Other  records  and  reports. — Washington  County:  Round  Top 
Mountain,  near  Hancock  (bat  banding  record,  U.S.  Fish  and  Wild- 
life Service). 

Remarks. — The  skull  of  the  Maryland  specimen  is  small  in  all 
measures,  but  otherwise  appears  to  be  typical  M.  sodalis.  It  has  the 
slight  but  perfectly  defined  sagittal  crest  which  is  generally  present 
in  this  species  and  lacking  in  M.  lucifugus.  Unfortunately,  the  skin  is 
missing  from  the  National  Museum  collections. 


MAMMALS  OF  MARYLAND 


47 


SMALL-FOOTED  MYOTIS 
Myotis  subulatus  leibii  (Audubon  and  Bachman) 

Vespertilio  leibii  Audubon  and  Bachman,  Jour.  Acad.  Nat.  Sci.  Phila- 
delphia, ser.  1,8: 284, 1842. 

Myotis  winnemana  Nelson,  Proc.  Biol.  Soc.  Wash.,  XXVI:  183,  8 
August  1913.  (Type  from  Plummers  Island,  Maryland.) 

Type  locality. — Brie  Ck)unty,  Ohio. 

General  distribution. — Ontario  and  southwestern  Quebec,  south  to  western 
North  Carolina,  and  west  to  southern  Iowa,  eastern  Kansas,  and  northeastern 
Oklahoma. 

Distribution  in  Maryland. — Recorded  from  Plummers  Island, 
Montgomery  County,  and  Round  Top  Mountain  near  Hancock,  "Wash- 
ington County.  This  species  probably  hibernates  in  caves  in  the  Alle- 
gheny Mountain  section,  and  passes  through  the  rest  of  the  State 
during  migrations. 

Distinguishing  characteristics. — Similar  to  Myotis  hicifugus,  but 
differs  in  its  smaller  size,  golden  tinted  fur,  black  ears,  black  facial 
mask,  and  shorter  forearm.  The  skull  is  much  flatter  than  that  of  M. 
lu/)ifugus,  and  the  braincase  narrower. 

Measurements. — Two  adults  from  Plummers  Island,  Montgomery 
County  (the  first  the  type  of  M.  winncTnana  Nelson)  measure  as  fol- 
lows :  Total  length  82,  80 ;  tail  vertebrae  39,  35 ;  hind  foot  8, 7 ;  greatest 


Myotis  subulatus    leibii 
#  Specimens  examined 
O  Specimens  reported 


Figure  17. — Distribution  of  Myotis  subulatus  leibii. 


4S  NORTH  AMERICANi  FAUNA  66 

length  of  skull  13.7,  13.1;  interorbital  breadth  3.4,  3.3;  length  of 
maxillary  toothrow  5.1, 5.0. 

Habitat  and  habits. — These  bats  probably  hibernate  in  caves  in  the 
wild  forested  regions  of  the  Allegheny  Mountains  and  migrate  else- 
where in  the  State  during  late  winter  and  early  spring.  Most 
specimens  have  been  taken  in  caves  located  in  hemlock  forests.  The 
position  of  these  bats  as  they  hang  on  the  walls  or  ceilings  of  the  caves 
is  a  definite  means  of  identification.  The  arms,  instead  of  hanging 
parallel  to  the  body,  as  generally  found  in  M.  lucifugus  and  other  bats, 
are  extended  about  30  degrees  from  the  vertical.  Little  is  known  of  the 
feeding  and  breeding  habits,  but  they  are  presumed  to  be  similar  to 
M.  lucifugus. 

Specimens  examined. — Montgomery  County:  Plummers  Island,  2. 

Other  records  and  reports. — Washington  Gownty:  Round  Top 
Mountain,  near  Hancock  (bat  banding  record,  U.S.  Fish  and  Wildlife 
Service) . 

SILVER-HAIRED  BAT 

Lasionycteris  noctivagans  (Le  Conte) 

Vl^espertilio'].  noctivagans  Le  Conte,  in  McMurtrie,  The  animal  king- 
dom ...  by  the  Baron  Cuvier,  vol.  1,  App.,  p.  431,  1831. 

Type  locality. — Eastern  United  States. 

General  distribution. — Nearly  all  of  North  America,  from  the  tree  line  in 
northern  Canada,  south  to  Georgia,  Texas,  New  Mexico,  and  California. 

Distribution  in  Maryland. — Probably  breeds  only  in  the  Allegheny 
Mountain  section,  but  occurs  in  all  sections  of  the  State  as  a  migrant 
in  the  spring  and  the  fall. 

Distinguishing  characteristics. — Teeth  2/3,  1/1,  2/3,  3/3,  =  36;  pelage 
dark  brownish-black,  the  ends  of  the  hairs  tipped  with  sUver,  giving 
a  somewhat  frosted  effect,  particularly  along  the  middle  of  the  back; 
fur  extends  onto  dorsal  surface  of  interfemoral  membrane;  ears  short 
and  rounded  with  broad,  blunt  tragus;  skull  flattened,  and  rostrum 
broad. 

Measurements. — An  adult  male  from  Plurmners  Island,  Montgomery 
County  has  the  following  external  measurements:  Total  length  116; 
tail  vertebrae  47;  hind  foot  10,  Some  cranial  measurements  of  four 
adults  from  Washington,  D.C.  are:  Greatest  length  15.8  (15.6-16.2)  ; 
zygomatic  breadth  (2  specimens)  9.9,  9.1;  interorbital  breadth  4.1 
(4.0-4.3) ;  length  of  maxillary  toothrow  5.7  (5.6-5.8). 

Habitat  and  habits. — This  bat  is  found  most  frequently  flying  about 
ponds  and  streams  in  wooded  areas.  It  roosts  in  hollow  trees,  in  dense 
foliage,  and  occasionally  in  buildings.  It  is  sociable  and  often  en- 
countered in  large  groups.  As  in  many  species  of  bats,  there  is  a  marked 


MAMMALS  OF  MARYLANI> 


49 


79-                                                                 76- 

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V 

76- 

r} 

p 

P*"^ 

Mill 

w 

-39°- 

SCA  LE 
O        lO      20      30MILES 

% 

m 

-33°- 

Lasionycteris  nootivagans 
#    Specimens   examined 
O    Specimens    reported 

^■liiiiiiiitf} 

-3B'- 

■x: 

i^M 

"X^ 

T                          T 

1 

76° 

BOM 

FiQUEE  18. — Distribution  of  Lasionycteris  noctivagans. 


segregation  of  the  sexes  and  the  large  colonies  seem  to  be  composed 
primarily  of  females.  Solitary  animals  are  usually  males. 

The  breeding  habits  of  this  species  are  not  well  known,  but  accord- 
ing to  Jackson  (1961,  p.  86)  it  usually  has  two  young,  bom  blind  and 
nearly  naked,  the  last  part  of  June  or  early  in  July.  The  young  remain 
clinging  to  the  breast  of  the  mother  until  they  are  about  3  weeks  old, 
when  they  are  able  to  fly  and  shift  for  themselves.  A  single  litter  is 
produced  each  year. 

The  silver-haired  bat  feeds  entirely  on  nocturnal  insects,  particularly 
those  that  fly  high  in  the  woodlands  or  over  the  borders  of  watercourses 
with  wooded  banks. 

Specimens  examined. — Montgomery  County :  Great  Falls,  1 ;  Plum- 
mers  Island,  1.  Prince  Georges  County:  Laurel,  1.  District  of  Colum- 
bia: 5. 

Other  records  and  reports. — Prince  Georges  County:  Patuxent  Re- 
search Center  (Gardner,  19506,  p.  112) . 

EASTERN  PIPISTRELLE 

Pipistrellus  subflavus  subflavus  (F.  Cuvler) 

Ylespertiliol.  subflavus  F.  Cuvier,  Nouv.  Ann.  Mus.  Hist.  Nat.  Paris, 
1 :  17,  1832. 

Type  locality. — Georgia,  restricted  to  the  LeConte  Plantation,  3  miles  SW  Rice- 
boro,  Liberty  County,  by  Davis  (1959,  p.  522) . 


so  NORTH  AMERICAN  FAUNA  66 

General  distribution. — From  central  Minnesota  and  southern  Quebec  south  into 
Georgia  and  western  Florida ;  west  to  Oklahoma,  Texas,  and  Tamaulipas.  The 
center  of  its  abundance  is  the  Ohio  River  Valley ;  north  of  this  it  occurs  locally 
in  summer  (Davis  and  Mumford,  1962,  p.  396). 

Distribution  in  Maryland. — Probably  ranges  throughout  all  sections 
of  the  State,  although  there  are  no  records  of  it  from  the  Eastern  Shore 
section. 

Distinguishing  characteristics.' — Teeth  2/3,  1/1,  2/2,  3/3,  =  34; 
smallest  bat  in  Maryland;  coloration  of  dorsum  grayish  to  reddish- 
brown,  each  hair  tricolored,  plumbeous  at  base,  dark  brown  at  tip, 
with  central  portion  yellowish-brown;  flight  weak  and  erratic,  giving 
the  animal  somewhat  the  appearance  of  a  large  fluttering  moth. 

Measurements. — External  measurements  of  11  adults  from  Washing- 
ton, D.C.,  are  as  follows :  Total  length  81.6  (75-90)  ;  tail  39.5  (37^2) ; 
hind  foot  8.5  (8.0-9.0).  Some  cranial  measurements  of  10  adults  from 
Washington  are  as  follows:  Greatest  length  12.8  (12.4-13.1)  ;  zygo- 
matic breadth  7.9  (7.7-8.2)  ;  interorbital  breadth  3.5  (3.4-3.6) ;  length 
of  maxillary  toothrow  4.3  (4.2-4.4) . 

Habitat  and  habits. — This  is  a  wide-ranging  species  that  hibernates 
in  caves,  mine  shafts,  and  rock  crevices.  During  the  summer  months  it 
probably  spends  the  daylight  hours  in  trees,  although  it  is  sometimes 
found  in  buildings.  It  is  most  frequently  encountered  in  wooded  areas 
near  water.  The  pipistrelle  is  believed  to  have  a  feeding  range  of  at 
least  5  or  6  miles,  and  a  homing  instinct  has  been  demonstrated  by 
tracing  banded  bats  for  distances  up  to  80  miles.  Individuals  roost 
year  after  year  in  the  same  cave. 

Mating  occurs  in  November,  and  young  are  born  the  last  part  of  June 
or  early  July.  Usually  two  constitute  a  litter,  but  there  are  occasionally 
triplets,  and  sometimes  only  a  single  offspring.  By  the  time  they  are 
about  a  month  old  they  are  able  to  fly,  and  shortly  thereafter  begin  to 
shift  for  themselves.  Since  pipistrelles  are  so  small  their  food  is  proba- 
bly restricted  to  insects  such  as  flies,  moths,  and  the  smaller  bugs  and 
beetles. 

Despite  their  diminutive  size,  pipistrelles  apparently  have  a  long 
life  span.  Banded  individuals  have  been  recovered  in  good  health  as 
long  as  10  years  after  they  were  originally  tagged. 

/Specimens  examined. — Anne  Arundel  County:  Magatha  R.  ( =  Ma- 
gothy  River?),  2.  Charles  County:  Marshall  Hall,  13.  Garrett  County: 
Near  Oakland,  1.  Montgomery  County:  Capitol  View,  1 ;  Glen  Echo,  1 ; 
Great  Falls,  1 ;  Plummers  Island,  2.  Prince  Georges  County:  Hyatts- 
ville,  1;  Laurel,  1;  near  D.  C.  line,  6.  St.  Marys  County:  St.  George 
Island,  4;  District  of  Columbia:  40. 

Other  records  and  reports. — Baltimore  County:  Bare  Hills  (Bures, 
1948:  64);  Orange  Grove  (Hampe,  1939:  5).  Washington  County: 


MAMMALS  OF  MARYLAND  51 


r                   r 

V 

76° 

'S 

p 

'§m^'m 

W//////^// 

M 

-39«- 

SC*  L  E                                                                ^^ 
O        lO      20      30MILES 

•iJ/u/!7f//j 

mW//m 

-33°- 

//»  ^]^  «^ Jf%' /  AY  / /yl 

Pipistrellus  subflavus  subflavus 
•    Specimens   examined 
0     Specimens    reported                                  ^ 

18 

'WJ/ff//M 

-38*- 

^^ 

%1 

f                   r 

1 

1 

76* 

BOM 

FiGUEE  19. — Distribution  of  Pipistrellus  subflavus  subflavus. 

Keedysville,  Snively's  Cave  No.  1  (bat  banding  record,  U.S.  Fish  and 
Wildlife  Service)  ;  Round  Top  Mountain  (bat  banding  record,  U.S. 
Fish  and  Wildlife  Service) . 

Remarks. — Two  subspecies  of  Pipistrellus  subflavus  have  been  named 
from  the  eastern  United  States,  P.  s.  subflavus^  the  typical  form  as 
described  above,  and  P.  s.  ohscums  Miller  (Type  locality :  Lake  George, 
Warren  County,  New  York).  Miller  (1897,  p.  93)  described  ohscums 
as  differing  from  subflavus  only  in  coloration,  being  somewhat  darker, 
duller,  and  more  yellowish.  Several  specimens  from  the  vicinity  of 
Washington,  D.C.,  in  the  national  collections,  are  darker  than  typical 
P.  s.  subflavus  and  were  referred  by  Bailey  (1923,  p.  136)  and  Gardner 
(1950b,  p.  112)  to  obscurus.  Bailey  (1923,  p.  137)  says  that  "They  may 
have  migrated  from  their  northern  habitat,  or  merely  wandered  out  of 
their  regular  range  after  the  breeding  season  was  over."  As  pointed 
out  by  W.  H.  Davis  ( 1959,  p.  523) ,  who  has  synonomyzed  P.  s.  obscurus 
with  P.  s.  subflavus,  there  is  a  wide  range  of  individual  variation  in 
color  in  this  species,  and  dark  specimens  are  found  throughout  the 
entire  range  of  P.  s.  subflavus.  The  dark  specimens  from  the  vicinity 
of  Washington,  referred  to  obscurus  by  both  Bailey  and  Gardner,  fall 
within  the  range  of  individual  variation  of  color  in  the  subspecies 
subflavus. 

Another  Maryland  specimen  which  exhibits  atypical  coloration  is 
from  St.  George  Island,  St.  Marys  County.  It  is  similar  to  P.  s.  florid- 


62 


NORTH  AMEBIGANi  FAUNA  66 


amis  Davis,  which  is  distributed  over  peninsular  Florida  and  south- 
eastern Georgia.  W.  H.  Davis  (1957,  p.  215)  speculated  that  perhaps 
this  animal  actually  was  a  -fioridanus  that  had  wandered  northward. 
In  a  later  publication  ( 1959,  p.  524) ,  however,  he  says  that  unless  it  can 
be  shown  that  this  actually  happened  it  is  best  to  refer  this  specimen 
to  P.  s.  subfiavus.  The  specimen  has  been  in  the  National  collections 
for  many  years  (collected  20  August  1887) ,  and  the  unusual  coloration 
is  perhaps  due  to  fading. 

BIG  BROWN  BAT 

Eptesicus  fuscus  fuscus  (Palisot  de  Beauvois) 

Vespertilio  fuscus  Palisot  de  Beauvois,  Catalogue  Raisonne  du  Museum 
de  Mr.  C.  W.  Peale,  Philadelphia,  p.  18  (p.  14  of  English  ed.  by 
Peale  and  Beauvois) ,  1796. 

Type  locality. — Philadelphia,  Pa. 

General  distribution. — Eastern  North  America,  from  Quebec,  Ontario,  and 
Manitoba,  south  into  Florida  and  Nuevo  Leon,  Mexico. 

Distribution  in  Maryland. — Abundant  in  the  lower  Piedmont  and 
upper  Western  Shore  sections  in  the  vicinity  of  the  fall  line.  Uncom- 
mon in  the  Allegheny  Mountain,  Ridge  and  Valley,  and  Eastern  Shore 
sections. 


Eptesicus  fussus  fuscus 
•  Specimens  examined 
O  Specimens  reported 


Figure  20. — Distribution  of  Eptesicus  fuscus  fuscus. 


MAMMALS  OF  MARYLAND  53 

Distinguishing  characteristics. — Teeth  2/3,  1/1,  1/2,  3/3,  =  32;  size 
large,  exceeded  in  Maryland  only  by  the  hoary  bat;  coloration  uni- 
formly dark  brown;  ears  thick  and  heavy,  somewhat  rounded  and 
medium  in  size,  naked  except  for  some  fur  at  the  base;  wings  and  inter- 
femoral  membrane  lacking  fur;  skuU  larger  and  heavier  than  any  other 
local  bat  except  Lasiurus  cinereus,  from  which  it  differs  in  being  notice- 
ably narrower.  Both  Eptesicus  and  Lasiurus  have  32  teeth,  but  in 
Eptesicus  there  are  2  upper  incisors  and  1  upper  premolar,  while  in 
Lasiurus  there  are  2  upper  premolars  and  1  upper  incisor  on  each  side. 

Measurements. — External  and  cranial  measurements  of  15  adults 
from  Washington,  D.C.,  are  as  follows :  Total  length  113.2  (110-122) ; 
tail  43.6  (40^8) ;  hind  foot  (average  of  9)  12  (10-13)  ;  greatest  length 
of  skull  18.5  (17.5-19.6)  ;  zygomatic  breadth  (average  of  10)  12.6 
(12.1-13.4) ;  interorbital  breadth  4.2  (3.9-4.5) ;  length  of  maxillary 
toothrow7.1  (6.9-7.4). 

Habitat  and  habits. — This  bat  usually  occurs  around  buildings  and 
dwellings  where  it  roosts  in  the  daytime  under  windowsills,  in  the  eaves 
of  roofs,  in  cracks  or  crevices,  or  behind  doors,  blinds,  and  awnings. 
It  is  sometimes  found  in  hollow  trees,  under  loose  bark,  and  occasionally 
in  caves  or  crevices  in  cliffs.  This  species  is  common  in  parts  of  Mary- 
land ;  it  is  an  unusual  year  when  at  least  one  specimen  is  not  captured 
in  the  Natural  History  building  of  the  National  Museum  and  added 
to  the  study  collection.  The  big  brown  bat  does  not  form  large  colonies 
as  do  some  species  of  bats.  Probably  it  is  in  part  migratory,  but  does  not 
engage  in  extensive  seasonal  migrations,  other  than  to  find  a  suitable 
place  for  hibernation.  This  is  one  of  the  last  bats  to  hibernate  in  the 
fall,  and  it  is  on  wing  again  in  early  March.  During  mild  spells  of 
winter  it  may  be  seen  flying  in  the  sun  at  midday  (Hamilton,  1943, 
p.  90) .  These  bats  are  long-lived ;  records  of  banded  animals  recovered 
10  to  15  years  later  are  numerous. 

The  homing  instinct  seems  to  be  develqped  to  some  degree.  Cohen 
(1944)  found  several  adults  behind  the  shutter  of  a  house  in  Berwyn, 
Prince  Georges  County,  and  after  banding  them  released  them  on  4 
October  1941,  in  Baltimore  City.  Twelve  days  later,  on  15  October  1941, 
one  of  these  bats  was  found  hanging  on  the  same  shutter  from  which 
it  had  been  removed  in  Berwyn.  It  had  travelled  a  distance  of  26.56 
miles,  over  the  congested  city  of  Baltimore,  and  heavily  travelled  high- 
ways, to  return  to  its  home  roost. 

The  mating  season  for  the  big  brown  bat  is  September,  and  young  are 
born  the  following  June.  Normally  two  comprise  a  litter,  although 
there  may  occasionally  be  only  one.  The  young  grow  rapidly  and  3  or 
4  weeks  after  birth  are  able  to  shift  for  themselves. 

This  species,  like  all  Maryland  bats,  is  primarily  insectivorous. 
Hamilton  (1933a)  examined  2,200  summer  fecal  pellets  from  northern 


54  NORTH  AMERICANi  FAUNA  66 

West  Virginia  and  concluded  that  the  most  common  insects  consumed 
by  the  big  brown  bat  in  summer  are  (in  order  of  abundance  of  re- 
mains) :  Coleoptera,  Hymenoptera,  Diptera,  Plecotera,  Ephemirida, 
Hemiptera,  Tricoptera,  Neuroptera,  Mecotera  and  Northoptera.  No 
lepidqpterous  remains  were  discovered  by  Hamilton  in  the  pellets. 

Specimens  esoamined. — Baltimore  Oity :  1.  Baltimore  County:  Ca- 
tonsville,  1.  Montgornery  County:  Kensington,  1;  Plummers  Island, 
2 ;  Silver  Spring,  1 ;  Takoma  Park,  2.  Prince  Georges  County :  Laurel, 
3.  District  of  Columbia:  86. 

Other  records  and  reports. — Awfie  Arundel  County:  Jessup  (Silver, 
1928,  p.  149).  Baltimc/re  County:  Bare  Hills  (Cohen,  1942,  p.  96)  ; 
Patapsco  State  Park  (Hampe,  1939,  p.  5).  Montgomery  County: 
Washington  Grove  (Christian,  1956,  p,  66).  Prince  Georges  County: 
Berwyn  (Cohen,  1944,  p.  65) ;  Patuxent  Research  Center  (Gardner, 
19505,  p.  112) .  Washington  County:  Round  Top  Mountain,  near  Han- 
cock (banding  record). 

RED  BAT 
Lasiurus  borealis  borealis  (Mtiller) 

Vespertilio  horealis  Miiller,  Des  Ritters  Carl  von  Linne  .  .  .  voll- 
standiges  Natursystem  nach  der  zwolften  lateinischen  Ausgabe.  .  . . 
Suppl.  (Mammalia) ,  p.  20, 1776. 

Type  locality. — New  York 

General  distribution. — Eastern  North  America,  from  southern  New  Brunswick, 
Quebec,  Ontario,  Manitoba,  Saskatchewan,  and  Alberta,  south  to  Florida  and 
Texas. 

Distribution  in  Maryland. — Abundant  in  all  sections  of  the  State. 

Distinguishing  characteristics. — Teeth  1/3,  1/1,  2/2,  3/3,  =  32;  size 
medium;  color  bright  rufous  or  fulvous,  hairs  plumbeous  at  base  and 
whitish  at  tips,  producing  a  slight  frosted  effect;  ears  broad  and  blunt, 
rounded  at  tip,  reaching  about  halfway  from  the  angle  of  the  mouth 
to  the  nostril  when  laid  forward;  tail  moderately  long;  interfemoral 
membrane  thickly  furred  on  upper  surface. 

This  bat  is  easily  distinguished  from  all  other  bats  in  Maryland  by 
its  bright  rufous  coloration  and  the  furred  interfemoral  membrane. 
Males  generally  are  darker  and  more  reddish  than  females. 

MeasureTnents. — ^An  adult  male  from  Doubs,  Frederick  County,  and 
an  adult  female  from  3  miles  NW  of  Annapolis,  Anne  Arundel 
County,  measure  respectively:  Total  length  109,  113;  tail  49,  50;  hind 
foot  10,  7 ;  greatest  length  of  skull  13.0,  12.6 ;  zygomatic  breadth  9.5, 
9.5 ;  interorbital  breadth  4.4,  4.2 ;  length  of  maxillary  toothrow  4.6, 4.4. 

Habitat  and  habits. — This  bat  shows  a  preference  for  deciduous 
woodlands,  orchards,  and  city  parks  with  trees  and  tall  shrubs.  It 
generally  chooses  the  branch  of  a  shady  tree  in  which  to  roost,  some- 


MAMMALS  OF  MARYLAND 


55 


Lasiurus  borealis  borealis 
9  Specimens  examined 
O  Specimens  reported 


Figure  21. — Distribution  of  Lasiurus  borealis  borealis. 


times  within  a  few  feet  of  the  ground,  and  conceals  itself  in  the  foliage. 

It  is  well  known  that  the  red  bat  is  migratory  in  habits,  spending 
smnmers  in  northern  areas  and  flying  south  in  the  autumn.  They  are 
not  found  in  the  winter  in  the  more  northern  areas,  while  their  num- 
bers appear  to  increase  in  the  south.  In  Maryland  they  apparently 
occur  the  year  round,  specimens  having  been  taken  in  all  months 
from  April  through  December,  and  in  nearby  Arlington,  Va.,  on 
1  March.  Whether  the  same  population  occurs  here  in  the  summer 
as  in  the  winter  is  not  known.  Perhaps  the  summer  population  migrates 
farther  south  and  its  place  is  taken  by  a  more  northern  population 
which  has  migrated  in. 

It  appears  that  this  bat  migrates  southward  in  the  fall  behind  an 
advancing  cold  front.  David  Bridge,  a  Maryland  bird  bander,  tells 
me  that  he  often  takes  red  bats  in  the  autumn  in  his  bird  nets  at  Kent 
Point  on  Kent  Island,  Queen  Annes  County,  for  several  days  following 
the  movement  of  a  cold  front  through  the  area. 

The  red  bat  is  a  strong  swift  flyer.  Jackson  (1961,  p.  96)  states  that 
observational  timing  he  made  of  it  would  indicate  an  ordinary 
straightaway  flying  speed  of  near  40  miles  per  hour.  It  has  sometimes 
been  observed  flying  far  out  to  sea  as  much  as  500  miles  from  the 
nearest  land.  Usually  it  migrates  at  night,  but  occasionally  it  is  ob- 
served during  the  day.  A.  H,  Howell  (1908,  p.  36)  observed  over  a 


56  NORTH  AMERICAN,  FAUNA  66 

hundred  bats,  most  of  which  were  probably  of  this  species,  passing 
over  a  part  of  Washington,  D.C.,  between  9  and  10  a.m.  on  the  cloudy 
mild  morning  of  28  September  1907. 

Red  bats  mate  during  early  August;  copulation  occurs  while  the 
bats  are  in  flight.  The  female  apparently  stores  the  sperm,  and  the 
young  are  not  born  until  the  following  June  after  a  gestation  period 
of  80  to  90  days.  Three  are  the  usual  number  of  young  per  litter, 
although  there  are  occasionally  two  or  four. 

Like  other  Maryland  bats,  the  red  bat  is  insectivorous  and  catches 
most  of  its  prey  while  on  wing.  Some  insects,  however,  are  probably 
taken  from  the  foliage  or  even  near  the  ground,  since  remains  of 
crickets  have  been  found  in  stomachs.  Additional  items  of  diet  are 
flies,  bugs,  beetles,  cicadas,  and  other  insects. 

Specimens  exaTnined. — Anne  Anmdel  Counts/:  Annapolis,  1;  An- 
napolis, 3  miles  NW,  1 ;  no  exact  locality,  2.  Baltimore  City:  1.  Calvert 
County:  Solomons,  1.  Charles  County:  Port  Tobacco,  li^  miles  SW, 
2.  Dorchester  County:  Cambridge,  1.  Frederick  County:  Doubs,  1. 
Montgomery  County:  Forest  Glen,  6 ;  Glen  Echo,  1 ;  Plummers  Island, 
7;  Silver  Spring,  2.  Prinwe  Georges  County:  College  Park,  1;  Laurel, 
14.  Somerset  County:  off  Tangier  Island,  Virginia,  1;  'Washington 
County:  Hagerstown,  2;  Sandy  Hook,  1.  District  of  Columhiu:  83. 

Other  records  and  reports. — Baltimore  County:  Patapsco  State  Park 
(Hampe,  1939,  p.  5).  Queen  Annes  County:  Kent  Point  (bird  bander 
David  Bridge  in  verbis,  16  September  1964) . 

Remarks. — A  closely  related  species,  the  seminolebat,  Lasiurus  semi- 
nolus  (Rhoads),  which  normally  is  found  in  Florida,  southern  Geor- 
gia, Alabama,  Mississippi,  and  Louisiana,  has  been  reported  twice 
from  southeastern  Pennsylvania  (Poole,  1932,  p.  162;  1949,  p.  80) 
and  once  from  central  New  York  (Layne,  1955,  p.  453) .  Layne  suggests 
that  individuals  of  this  species  may  wander  northward  far  out  of  the 
norm.al  range  in  summer,  and  if  this  is  so,  the  seminole  bat  may  eventu- 
ally be  taken  in  Maryland.  This  species  is  distinguished  from  the  red 
bat  by  its  much  darker  coloration,  a  rich  mahogany  brown  slightly 
frosted  with  white. 

HOARY  BAT 

Lasiurus  cinereus  cinereus  (Palisot  de  Beauvois) 

VespertUio  cinereus  (misspelled  linereus)  Palisot  de  Beauvois,  Cata- 
logue raisonne  du  museum  de  Mr.  C.  W.  Peale,  Philadelphia, 
p.  18, 1796. 

Type  locality. — Philadelphia,  Pa. 

General  distribution. — Most  of  North  America,  from  the  Atlantic  to  the  Pa- 
cific, north  into  Canada,  and  south  into  Mexico.  Breeds  in  the  northern  part  of 
its  range,  mostly  north  of  the  United  States. 


MAMMALS  OF  MARYLAND 


57 


Lasrurus  cmereus  ctnereus 
#  Specimens  examined 
O  Specimens  reported 


Figure  22. — Distribution  of  Ldsiurus  cinereus  cinereus/i. 


Distribution  in  Maryland. — Occurs  as  a  migrant  in  all  sections  of  the 
State;  may  breed  in  the  higher  portions  of  the  Allegheny  Momitain 
section. 

Distinguishing  characteristics. — Teeth  as  in  L.  horealis;  size  large 
(averaging  135  mm  in  total  length) ;  wingspread  averaging  around  14 
inches;  coloration  a  mixture  of  grayish  umber  and  chocolate  brown, 
heavily  tinged  with  white,  so  as  to  produce  a  hoary  effect,  especially  on 
the  back;  head  blunt,  with  ears  large  and  rounded,  conspicuously 
rimmed  with  black  or  dark  brown ;  tail  medium  length,  about  40  per- 
cent of  total  length  of  the>  animal;  interfemoral  membrane  thickly 
furred  on  upper  surface  nearly  to  the  edge;  anterior  edge  of  under- 
side of  wing  furred  for  about  half  its  length.  This  bat  is  easily  dis- 
tinguished from  all  other  Maryland  bats  by  its  large  size  and  unique 
coloration. 

Measurements. — ^Measurements  of  an  adult  male  from  Washington, 
D.C.,  are  as  follows :  Total  length  135.5 ;  tail  61.5 ;  hind  foot  13 ;  great- 
est length  of  skull  16.1;  zygomatic  breadth  12.0;  interorbital  breadth 
4.9 ;  length  of  maxillary  toothrow  6.2. 

An  adult  female  from  Washington,  D.C.,  has  the  following  cranial 
measurements :  Greatest  length  of  skull  16.9 ;  zygomatic  breadth  12.7 ; 
interorbital  breadth  5.5 ;  length  of  maxillary  toothrow  6.2. 

Habitat  and  habits. — This  is  a  migratory  species.  It  breeds  and 
spends  the  summer  in  the  northern  part  of  its  range,  from  southeast- 


58  NORTH  AMERICAN,  FAUNA  06 

ern  Pennsylvania  and  possibly  the  higher  mountains  of  the  Appa- 
lachians, north  into  Canada.  It  migrates  southward  quite  late  in  the 
season.  It  prefers  to  roost  in  coniferous  forests,  but  may  also  be  found 
in  farmyards,  city  parks,  and  yards,  particularly  where  coniferous 
trees  are  growing.  The  hoary  bat  has  an  extensive  home  range  and 
may  fly  a  mile  or  more  from  its  roosting  site  in  search  of  food.  It  is  a 
strong  and  rapid  flyer,  and  Jackson  (1961,  p.  100)  estimates  that  it 
can  achieve  speeds  of  up  to  60  miles  an  hour.  The  scarcity  of  records 
and  specimens  from  Maryland  indicates  that  it  is  rare  here.  In  the 
summer,  it  occurs  in  the  higher  mountains  of  the  Allegheny  Mountain 
section.  In  other  seasons,  it  may  be  encountered  throughout  Maryland. 

Little  is  known  of  the  breeding  habits  of  this  bat.  Jackson  (1961, 
pp.  100-101)  says  that  mating  probably  occurs  in  September  or  Octo- 
ber and  the  young  are  bom  in  May  or  June,  thus  giving  an  apparent 
gestation  period  of  about  8  months.  It  seems  probable,  however,  that 
as  in  some  other  species  of  bats  spermatozoa  survive  in  the  uterus 
through  the  winter,  and  that  fertilization  takes  place  early  in  the 
spring,  giving  an  actual  gestation  period  of  about  90  days.  Usually, 
two  yoimg  comprise  a  litter,  although  it  is  possible  that  as  many  as 
four  may  be  produced. 

The  hoary  bat  is  primarily  an  insect  feeder,  but  occasionally  preys 
on  smaller  bats. 

Specimens  examined. — Balfi<more  County:  Cockeysville,  1.  Prinze 
Georges  County:  Laurel,  1.  District  of  Columbia:  3. 

Other  records  and  reports. — Baltimore  City  (Merriam,  1887,  p.  86) . 
Prince  Georges  County:  Berwyn  (Tromba,  1954,  p.  253) . 

EVENING  BAT 
Nycticeius  humeralis  humeralis  (Rafinesque) 

Vespertilio  huineralis  Rafinesque,  American  Monthly  Mag.,  3  (6)  :  445, 
October  1818. 

Type  locality. — Kentucky. 

General  distribution. — From  Pennsylvania,  Michigan,  and  Illinois,  south  into 
Florida  and  Texas,  and  west  into  eastern  Oklahoma  and  Kansas. 

Distribution  in  Maryland. — Probably  absent  in  the  higher  moun- 
tains of  the  Allegheny  Mountain  and  Ridge  and  Valley  sections,  but 
elsewhere  it  may  occur  sparingly  as  a  summer  resident. 

Distinguishing  characteristics. — Teeth  1/3,  1/1,  1/2,  3/3,  =  30;  super- 
ficially resembles  Myotis  but  can  be  easily  distinguished  by  the 
reduced  number  of  teeth  and  the  short  sparse  brown  fur  which  is  dull 
umber  above  and  plumbeous  at  the  base;  fur  on  abdomen  paler  than 
on  dorsum;  ears  small  and  thick.  The  young  of  this  species  are  con- 
siderably darker  than  the  adults. 


MAMMALS  OF  MARYLAND 


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Nyctiaeius  humeralis  humeralis 

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FiGUBE  23. — Distribution  of  Nycticeius  humeralis  humeralis. 

Measurements. — ^Three  adults  from  the  vicinity  of  Washington, 
D.C.,  have  external  measurements  as  follows :  Total  length  90,  95,  94 ; 
tail  39,  35,  35 ;  hind  foot  10,  9,  8.  Six  adults  from  the  vicinity  of  Wash- 
ington have  the  following  cranial  measurements :  Greatest  length  14.2 
(13.7-15.5) ;  zygomatic  breath  9.7  (9.6-10.0) ;  interorbital  breadth  3.9 
(3.8-4.0) ;  maxillary  tocthrow  5.2  (5.0-5.4). 

Habitat  and  habits. — ^This  is  essentially  a  southern  species  that  wan- 
ders north  in  summer  sometimes  as  far  as  Pennsylvania,  Michigan,  and 
Illinois.  It  prefers  to  roost  in  hollow  trees,  flying  out  with  a  slow  and 
steady  flight  as  darkness  falls.  It  gives  birth  to  two  young,  generally 
in  late  May.  Little  else  is  known  of  its  habits  or  life  history. 

Specimens  examined. — Montgomery  County :  Linden,  1 ;  Plummers 
Island,  1;  Silver  Spring,  1.  Prince  Georges  County:  Hyattsville,  2; 
Oxon  Hill,  1 ;  near  D.C.  line,  1.  District  of  Columbia:  6. 

(BIG-EARED  BAT) 
Plecotus  townsendii  virginianus  (Handley) 

Corynorhynus  virginianus  Handley,  Jour.  Washington  Acad.  Sci.,  45 
(2)  :  148, 23  May  1955. 

Type  looality. — Schoolhouse  Cave,  4.4  miles  NE  of  Riverton,  2,205  feet,  Pendle- 
ton County,  W.  Va. 

General  distril)ution. — Central  part  of  the  Appalachian  highlands  in  eastern 
Kentucky,  western  Virginia,  and  eastern  West  Virginia. 


eO  NORTH  AMERICAN  FAUNA  66 

Distribution  in  Maryland. — Not  as  yet  recorded,  but  should  be  looked 
for  in  the  higher  portions  of  the  Allegheny  Mountain  section.  To  date 
it  has  not  been  found  resident  in  any  Maryland  caves,  but  it  probably 
enters  the  State  on  feeding  forays  from  caves  in  nearby  West  Virginia 
and  Virginia. 

Distinguishing  characteristics. — Teeth  2/3,  1/1,  2/3,  3/3,  =  36,  ears 
very  long;  glandular  masses  on  nose  appear  as  lumps;  fur  long  and 
limp;  colored  a  dark  brown  above,  and  pinkish  buff  on  belly,  inter- 
femoral  membrane  naked. 

The  very  large  ears  serve  to  distinguish  this  bat  from  any  others 
that  may  be  encountered  within  Maryland. 

Measurements. — Handley  (1959,  p.  233)  gives  some  measurements 
of  a  series  of  adults  from  West  Virginia  as  follows :  Total  length  101 
(98-103) ;  tail  vertebrae  50  (48-52) ;  hind  foot  11  (10-12)  ;  ear  from 
notch  34  (31-38)  ;  greatest  length  of  skull  16.5  (16.2-16.8) ;  zygomatic 
breadth  8.8  (8.6-9.0) ;  interorbital  breadth  3.7  (3.6-3.9) ;  length  of 
maxillary  toothrow  5.3  (5.2-5.4). 

Habitat  and  habits. — This  is  a  true  cave  bat  usually  roosting  in  small 
groups  and  emerging  at  dusk  to  fly  at  considerable  heights.  After  dusk 
it  descends  nearer  the  ground,  sometimes  at  an  elevation  of  only  sev- 
eral feet,  searching  for  insect  prey.  When  roosting  in  the  caves  during 
the  day,  the  long  ears  are  spirally  coiled  and  flattened  against  the  neck. 
It  is  a  shy  bat,  quick  to  take  alarm.  With  its  large  ears,  it  can  detect 
the  least  sound  and  seems  to  be  more  wary  than  other  species. 

Although  Pearson  et  al.  (1952)  have  made  a  detailed  study  of  the 
life  history  of  the  western  subspecies  of  Plecotus  townsendii.,  little  is 
known  concerning  the  habits  of  the  eastern  race.  Since  the  two  are 
widely  separated  geographically,  much  of  Pearson's  findings  may  not 
be  applicable  to  the  eastern  form.  Hamilton  (1943,  pp.  102-103)  says 
that  the  eastern  race  bears  its  young  during  late  June  and  that  the 
mother  carries  the  single  offspring  until  it  becomes  too  heavy.  As  with 
other  vespertilionid  bats,  the  spermatozoa  are  probably  stored  over 
winter  in  the  uteri  of  the  females  and  are  capable  of  fertilizing  in  the 
spring. 

This  species  is  insectivorous,  and  Hamilton  (1943,  p.  104)  says  that 
those  examined  for  a  clue  to  their  feeding  habits  contained  only  the 
remains  of  Lepidoptera  in  their  stomachs. 

Remarks. — This  bat  has  never  been  taken  within  Maryland,  but  has 
been  found  in  several  caves  very  close  to  the  border  of  the  western  part 
of  the  State,  in  Grant,  Preston,  and  Tucker  Counties,  W.  Va. 

During  the  Pleistocene,  a  bat  very  similar  to  this  species  did  inhabit 
Maryland  caves.  Gidley  and  Gazin  (1933,  p.  345)  described  Oorynor- 
hynus  alleganiensis  {=  Plecotus  alleganiensis)  from  Pleistocene  de- 
posits in  Cumberland  Cave,  Allegany  County,  Md.  Handley  (1959,  p. 


MAMMALS  OF  MARYLAND  61 

210)  states  that  P.  alleganiensis  was  similar  in  many  respects  to  (and 
possibly  directly  ancestral  to)  P.  toionsendii. 

Order  LAGOMORPHA  (rabbits,  hares,  etc.) 

Family  LEPORIDAE  (rabbits,  hares) 

EASTERN  COTTONTAIL 

Sylvilagus  floridanus  mallurus  (Thomas) 

Llepus].  n\uttalli\.  mallurus  Thomas,  Ann.  Mag.  Nat.  Hist.,  ser.  7, 
2 :  320,  October  1898. 

Type  locality. — Raleigh,  N.C. 

General  distribution. — ^Primarily  east  of  the  Appalachian  Mountains,  from 
Massachusetts,  south  into  central  Florida,  west  to  Tennessee  and  Alabama. 

Distribution  in  Maryland. — Occurs  abundantly  in  all  sections  of  the 
State.  Cottontails  have  been  introduced  into  parts  of  Maryland  from 
areas  outside  the  range  of  mallurus,  and  hence  all  population  m  the 
State  may  not  be  ref  errable  to  that  race. 

Distinguishing  characteristics. — Teeth  2/1,  O/O,  3/2,  3/3,  =  28;  size 
small;  ears  large,  pelage  long  and  coarse,  reddish  brown,  mixed  with 
black  on  the  dorsum;  underparts  white,  including  the  underside  of 
the  tail;  nape  and  legs  cinnamon-rufous.  This  species  differs  from  the 
New  England  cottontail  {S.  transitionalis) ,  which  has  not  yet  been 
taken  in  Maryland  but  which  probably  occurs  in  the  mountains  of 
the  western  part  of  the  State,  in  several  external  and  cranial  characters 
which  are  described  under  that  species. 

Measurements. — External  measurements  of  three  adidts  from  the 
three  adults  from  Washii.gton,  D.C.,  are:  Basilar  length  57.5,  57.0, 

458 ;  tail  60,  64,  75 ;  hind  foot  99,  84, .  Cranial  measurements  of 

three  adults  from  Washington  D.C.,  are:  Basilar  length  57.5,  57.0, 
56.5 ;  zygomatic  breadth  36.9,  36.5,  36.3;  interorbital  breadth  19.1, 18.5, 
17.9 ;  length  of  maxillary  toothrow  14.1, 14.0, 13.2. 

Habitat  and  habits. — This  rabbit  occupies  a  variety  of  habitats  from 
the  marshes  of  the  Dehnarva  Peninsula  to  the  fields  and  meadows  of 
western  Maryland.  It  is  seldom  encomitered  in  heavy  woods.  It  occurs 
on  Assateague  Island,  off  the  Atlantic  coast  of  Maryland,  where  it 
is  particularly  abundant  in  the  wooded  thickets  and  dry  sandy  areas 
adjacent  to  the  marshes.  These  rabbits  are  found  in  the  tall  grass  and 
thickets  in  villages  and  towns  and  even  in  the  large  cities  such  as  Balti- 
more and  Washington.  The  summer  food  consists  of  almost  any  type  of 
green  vegetation,  but  it  seems  to  be  especially  fond  of  legumes,  dande- 
lions, plantains,  and  lettuce.  During  winter  it  eats  tender  parts  of 
many  shrubs  and  trees  and  will  gnaw  away  the  bark  of  some  species  of 

336-897  O — 69 5 


62 


NORTH  AMERICAN,  FAUNA  e6 


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Sylvitag-us  floridanus  mallwms 
•     Specimens   examined 

mMM 

O     Specimens    reported                               \j 

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FiGUBE  24 — Distribution  of  Sylvilagus  floridanus  mallurus. 


trees.  With  the  deforestation  of  much  of  Maryland  since  O)lomal 
times  the  cottontail  has  found  more  suitable  habitat  and  today  is 
abundant  throughout  the  State. 

The  cottontail  is  both  diurnal  and  nocturnal,  but  is  most  active 
during  the  first  3  or  4  hours  after  daylight  and  from  2  to  3  hours  be- 
fore sunset  to  about  1  hour  after  sunset.  It  does  not  hibernate,  but  is 
active  yearlong.  Cottontails  are  solitary  and  seldom  are  two  or  more 
found  together  except  in  the  case  of  mother  and  young. 

The  female  builds  a  brood  nest  of  grass  combined  with  fur  plucked 
from  her  own  abdomen.  The  nest,  placed  in  a  depression  in  the  ground, 
is  about  4  or  5  inches  in  diameter  and  depth.  It  is  usually  well  con- 
cealed in  grass,  weeds,  thickets,  or  scrubby  woods.  In  addition  to  the 
brood  nest,  the  cottontail  makes  forms  that  are  used  as  hiding  or  rest- 
ing places.  These  forms  are  made  by  scratching  or  trampling  a  shallow 
oval  hollow  in  the  ground  and  sometimes  lining  it  with  grass,  leaves, 
or  fur. 

Cottontails  in  Maryland  mate  in  late  winter.  The  gestation  period 
varies  from  28  to  32  days,  and  the  first  litter  of  the  year  appears  by 
mid-March.  Two  or  three  litters  are  produced  each  season,  and  the 
number  of  young  per  litter  varies  from  three  to  six,  with  five  being 
the  most  frequent. 

Specimens  examined. — Charles  County:  Marshall  Hall,  1;  Rock 
Point,  1.  Garrett  County:  Grantsville,  1.  Hoicdrd  County:  Long  Cor- 


MAMMALS  OF  MARYLAND  63 

ner,  2.  Montgomery  Gownty:  Kensington,  1 ;  Plummers  Island,  2;  Ta- 
koma  Park,  1;  no  exact  locality,  1.  Prince  Georges  County:  Clinton, 
1 ;  East  Riverdale,  1 ;  Lanham,  1 ;  Westwood,  1 ;  no  exact  locality,  3. 
District  of  Colwnbia:  24  (many  of  tliese  are  labeled  "purchased  in 
Washington  Market"  and  were  probably  taken  outside  the  District  of 
Ck>luinbia  area) . 

Other  records  and  reports. — Allegany  County:  Oldtown,  9  miles  E 
(personal  o'bservation).  Baltimore  City:  (personal  observation). 
Baltimore  County:  Bare  Hills-Lake  Eoland  area  (Bures,  1948,  p.  68) ; 
Loch  Raven  (Kolb,  1938) ;  Gwynnbrook  State  Game  Farm  (Sheffer, 
1957,  p.  90);  Patapsco  State  Park  (Hampe,  1939,  p.  7).  Howard 
County:  Atholton  (personal  observation).  Kent  County:  Ghestertown 
(U.S.  Fish  and  Wildlife  Service  files).  Prince  Georges  County:  Pa- 
tuxent  Research  Center  (Herman  and  Warbach,  1956,  p.  85).  Worces- 
ter County:  Assateagne  Island,  near  the  Virginia  border  (personal 
observation)  ;  Ocean  City,  1  mile  N  (personal  observation). 

Rernarks. — Nelson  (1909,  p.  168)  considers  the  specimen  from 
Grantsville  in  the  extreme  western  Allegheny  Mountain  section  to  be 
a  distinct  intergrade  with  S.  f.  nieamsi,  nearly  pale  enough  to  be  clas- 
sified with  meamsi. 

(NEW  ENGLAND  COTTONTAIL) 
Sylvilagus  transitionalis  (Bangs) 

Lepus  sylvaticus  transitionalis  Bangs,  Proc.  Boston  Soc.  Nat.  Hist., 
XXVI,  pp.  405-407, 31  January  1895. 

Type  locality. — Liberty  Hill,  New  London  County,  Conn. 

General  distribution — Distributed  from  southeastern  Maine,  southern  New 
Hamipshire,  and  Vermont,  south  through  eastern  New  York,  New  Jersey,  and 
eastern  Pennsylvania  and  along  the  Allegheny  Mountains  through  West  Virginia 
to  northern  Georgia  and  northeastern  Alabama. 

DistHhution  in  Maryland. — ^There  are  no  valid  records  of  the  New 
England  cottontail  from  Maryland,  but  it  almost  certainly  occurs  in 
the  Allegheny  Mountain  section  at  higher  elevations. 

Distinguishing  characteristics. — Similar  in  coloration  to  the  eastern 
cottontail,  except  that  the  underfur  is  a  much  darker  gray.  The  back 
is  ochraceous  buflP,  overlaid  with  a  wash  of  black-tipped  guard  hairs 
which  give  it  a  dark  appearance.  The  ears  are  short  and  round  and 
have  a  black  margin  on  the  outside  edge,  making  a  distinct  black 
line  which  does  not  blend  gradually  into  the  browner  color  of  the  ear 
as  in  the  eastern  cottontail.  A  definite  black  patch  is  between  and  just 
in  front  of  the  ears. 

Cranially  this  species  differs  from  the  eastern  cottontail  in  that  the 
skull  is  lighter  and  slenderer,  the  interorbital  breadth  narrower,  and 


64  NORTH  AMERICAN  FAUNA  66 

the  rostrum  thinner.  The  supraorbital  process  is  very  slender,  narrow- 
ing anteriorly  so  that  the  notch  is  absent,  or  virtually  so.  The  posterior 
portion  of  the  process  is  very  narrow  and  in  some  instances  is  free  of 
the  skull,  leaving  a  distinct  foramen.  The  auditory  bullae  are  notice- 
ably smaller  in  this  species  than  in  S.  floridanus. 

Measurements. — Nelson  (1909,  p.  168)  gives  average  measurements 
of  five  adults  from  Wilmington,  Mass.,  as  follows :  Total  length  388 ; 
tail  vertebrae  39 ;  hind  foot  96 ;  basilar  length  of  skull  54.8 ;  interor- 
bital  breadth  17.1. 

Since  geographic  variation  appears  to  be  slight  in  this  species, 
Maryland  specimens,  if  taken,  probably  would  not  differ  greatly  in 
size  from  the  Massachusetts  series. 

HabiUit  and  habits. — Llewellyn  and  Handley  (1945,  p.  384)  say 
that  in  Virginia 

All  specimens  examined  were  taken  at  elevations  above  3,000  feet  in  the  Alle- 
gheny Mountains.  Signs  indicate  that  these  cottontails  occupy  the  woods  and 
brush  along  most  of  the  higher  crests  and  ridges  of  the  state. 

They  believe  that  the  species  will  be  found  in  Virginia  only  at  ele- 
vations above  3,000  feet.  Since  the  species  occurs  in  the  Alleghenies 
to  the  north  and  south  of  Maryland,  and  since  there  are  several  moun- 
tains in  western  Maryland  that  exceed  3,000  feet  in  altitude,  it  is 
almost  certain  that  the  New  England  cottontail  is  resident  in  Maryland 
and  will  eventually  be  taken  there. 

This  species  is  similar  to  Sylvilagus  floridanus  with  regard  to 
breeding  habits  and  food  preferences. 

Remarks. — The  records  of  Nelson  (1909,  p.  199)  for  the  occurrence 
of  the  New  England  cottontail  in  Washington,  D.C.,  and  in  nearby 
Alexandria,  Va.,  have  been  shown  by  Bailey  (1923,  pp.  120-121)  to 
be  erroneous.  He  says : 

They  have  been  recorded  from  the  District  .  .  .  and  from  Alexandria,  but  the 
record  based  on  2  young  taken  in  a  nest  in  the  Soldiers  Home  grounds  by  Dr. 
O.  W.  Richmond  on  20  June  1886  was  erroneously  included  under  this  species, 
and  a  si>ecimen  which  I  bought  on  1  January  1904  of  a  colored  man  on  the  street 
who  said  he  killed  it  at  Alexandria,  probably  came  from  West  Virginia  where 
they  are  common  and  are  often  included  in  shipments  of  rabbits  to  market. 

SNOWSHOE  RABBIT 

Lepus  americanus  virginianus  Harlan 

Lepus  virginianus  Harlan,  Fauna  Americana,  p.  196, 1825. 

Type  locality. — Blue  Mountains,  near  Harrisburg,  Pa. 

General  distribution. — Southern  Ontario,  and  northeastern  United  States, 
from  southern  Maine,  south  in  the  Appalachian  Mountains  to  North  Carolina 
and  Tennessee. 


MAMMALS  OF  MARYLAND 


65 


SCA  LE 

o 

lO 

ZO 

30  MILES 

Lepus  ameriaanus   virginianus 

• 

Spec 

mens 

exami  ned 

O 

Spec 

mens 

reported 

Figure  25. — Distribution  of  Lepus  americcmus  virginianus. 


Distribution  in  Maryland. — Occurs  in  the  Allegheny  Mountain  and 
Ridge  and  Valley  sections  where  it  is  now  uncommon. 

Distinguishing  characteristics. — A  medium-sized  rabbit  with  large 
hind  feet  and  thick  fur.  Coloration  in  summer  pelage,  dull  rusty 
brown  varying  to  buffy  brown,  always  more  or  less  darkened  by  a  wash 
of  black.  In  winter,  coloration  is  sometimes  pure  white  with  a  little 
dusky  around  tips  of  ears;  but  frequently  a  dull  brownish  wash  is 
present  on  the  feet  and  terminal  half  of  the  ears. 

Cranially,  this  species  differs  from  Sylvilagus  floridanvs  and  S. 
transitionalis  in  its  larger  size  and  heavier  build,  with  much  stronger 
development  of  the  supraorbitals  which  are  subtriangular  and  stand 
out  broadly  winglike  with  a  broad  open  notch  between  the  posterior 
process  and  the  skull. 

Measurements. — Nelson  (1909,  p.  86)  gives  average  measurements 
of  five  adults  from  Pennsylvania  as  follows:  Total  length  518;  tail 
vertebrae  49;  hind  foot  414;  basilar  length  of  skull  65.0;  interorbital 
breadth  22.0. 

Habitat  and  habits. — This  rabbit  prefers  areas  of  spruce  in  the 
highest  regions  of  the  Allegheny  Mountain  and  Ridge  and  Valley 
sections,  where  it  has  been  observed  in  open  woods  and  thickets.  Spruce 
areas  are  small  and  scattered  districts  in  the  upland  swamps  and  on 
some  of  the  mountain  tops. 

Mansueti  (1953,  pp.  72-73)  says  that 


66  NORTH  AMERICAN  FAUNA  66 

The  varying  hare  seems  to  be  destined  to  permanent  extirpation  in  Maryland. 
It  is  a  species  with  specialized  habitat  requirements  and  one  of  limited  distribu- 
tion. Its  environment  is  being  encroached  upon  by  civilization  gradually  in  some 
and  swiftly  in  other  places.  .  .  .  The  optimum  habitat  is  forest  of  the  high  inter- 
mountain  Allegheny  Plateau  which  has  at  least  a  moderate  understory  of  small 
trees  and  shrubs  to  provide  food  and  cover.  These  areas  are  gradually  being 
destroyed  by  an  increasing  deer  herd  as  well  as  human  expansion  in  Garrett 
County. 

The  last  reliable  reports  of  snowshoe  rabbits  in  Maryland  were  by- 
John  Hamlet,  formerly  with  the  U.S.  Fish  and  Wildlife  Service,  who 
reported  that  in  1945  he  observed  a  female  in  Garret  County  but  did 
not  record  the  exact  locality,  and  by  John  Smith  of  Mountain  Lake 
who  shot  one  near  the  Holy  Cross  Camp,  Deep  Creek  Lake,  Garrett 
County,  in  March  1957.  This  latter  animal  was  probably  one  of  18  that 
had  been  shipped  into  the  country  from  the  Adirondacks  of  New  York 
and  released  in  March  1952.  (Maryland  Consei-vationist  34  (2),  p.  25, 
March  1957.) 

The  snowshoe  rabbit  is  active  in  the  summer  and  winter,  primarily 
early  in  the  morning  and  late  in  the  evening.  Although  it  constructs 
no  nests,  it  returns  to  the  same  spot  regularly  so  that  a  form  is  even- 
tually hollowed  out.  This  form  is  nearly  always  concealed  under  grass, 
brush,  shrubbery,  or  a  fallen  log. 

This  species  breeds  promiscuously.  Mating  begins  early  in  March 
and  may  continue  well  into  April.  The  first  litter  appears  in  April 
after  a  gestation  period  of  about  36  days ;  as  many  as  four  litters  a  year 
are  possible  during  a  breeding  season,  although  there  are  usually  only 
two.  The  number  of  young  may  range  from  one  to  five  or  more,  but 
most  frequently  three  or  four. 

Food  of  the  snowshoe  rabbit  in  summer  consists  of  dandelion, 
grasses,  clover,  ferns,  and  the  tender  parts  of  certain  shrubs  and  trees. 
In  winter,  when  many  summer  foods  are  not  available,  it  feeds  on 
bark  and  shoots  of  woody  plants. 

Specimens  examined. — Allegany  County:  Cumberland,  1. 

Other  records  and  reports. — Garrett  County:  Cranesville  Swamp 
area  (Mansueti,  1953,  p.  72)  ;  Deep  Creek  Lake  (Maryland  Conserva- 
tionist 34(2),  p.  25,  March  1957)  ;  Finzel  (Mansueti,  1953,  p.  72,  says 
that  a  specimen  from  this  locality  is  in  the  collections  of  the  U.S. 
National  Museum  and  lists  it  among  his  specimens  examined.  There  is 
no  record,  however,  that  a  specimen  from  Finzel  has  ever  been  in 
the  National  Museum  collections.  Rhodes  (1903,  pp.  119-120)  quotes 
Merriam  as  saying  that  Preble  was  told  of  the  occurrence  of  Lepus 
virginianus  at  Finzel,  Md.,  only  half  a  mile  from  the  Pennsylvania 
line.  Mansueti  may  have  confused  this  record  with  the  specimen  of 
Lepus  a.  virginianus  from  Cumberland,  Md.,  which  is  in  the  National 
Museum  collections,  and  which  is  probably  the  one  he  examined.) ; 


MAMMALS  OF  MARYLAND  67 

Little  Crossings,  headwaters  of  North  Branch  of  Castleman  River 
(Browning,  1928,  p.  242)  ;  Wolf  Swamp,  SE  of  Grantsville  (Mansueti, 
1953,  p.  Y2). 

Remarks. — Several  hundred  snowshoe  rabbits  have  been  stocked  at 
various  times  in  several  localities  in  western  Maryland,  None  of  these 
introductions  appear  to  have  been  very  successful,  although  the  speci- 
men taken  by  John  Smith  at  Deep  Creek  Lake  in  March  1957  seems 
to  be  one  of  those  stocked  in  1952. 

Order  RODENTIA  (gnawing  mammals) 

Family  SCIURIDAE  (squirrels) 

EASTERN  CHIPMUNK 

Tamias  striatus  (Linnaeus) 

[Sciurusl  striatus  Linnaeus,  Syst.  nat.,  ed.  10,  1 :  64, 1758. 

The  eastern  chipmunk  is  distributed  from  Quebec,  New  Brunswick, 
and  Nova  Scotia,  south  into  Georgia  and  Louisiana,  west  to  eastern 
Oklahoma,  Kansas,  Nebraska,  North  and  South  Dakota,  and  Saskatch- 
ewan. In  Maryland,  two  subspecies  are  recognizable.  They  are — 

Tamias  striatus  fisheri  A.  H.  Howell 

Twmms  striatus  fisheri  A.  H.  Howell,  J.  Mammal.,  6(1)  :  51,  9  Febru- 
ary 1925. 

Type  looality. — Merritts  Corners,  4  miles  E  of  Ossining  (Sing  Sing),  West- 
chester County,  N.Y. 

This  type  locality  has  been  the  source  of  some  confusion  in  the  literature. 
It  has  been  listed  by  various  authorities  as  "Merritt's  Corners,  four  miles  W  of 
Sing  Sing  [=  Ossining]  New  York,"  (Howell,  1925,  p.  51)  ;  "Merritts  Corners, 
4  miles  E  of  Ossining  (Sing  Sing),  N.Y.,"  (Howell,  1929,  p.  16);  "Merritts 
Corners,  4  miles  W  of  Sing  Sing  (Ossining),  Westchester  County,  N.Y.,"  (Poole 
and  Schantz,  1942,  p.  560)  ;  "Merritts  Corners,  4  miles  E  of  Ossining  (Sing  Sing), 
Westchester  County,  N.Y."  (Miller  and  Kellogg,  1955,  p.  218)  :  "Merritts  Corners, 
4  miles  W  Ossining  (Sing  Sing),  AVestchester  County,  N.Y.,"  (Hall  and  Kelson, 
19.59,  p.  294). 

The  confusion  involves  whether  Merritts  Corners,  a  small  New  York  State 
village  not  found  on  current  maps  of  the  region,  actually  lies  west  or  east  of 
Ossining,  N.Y.,  and  hence  west  of  the  Hudson  River  in  Rockland  County  or  east 
of  the  Hudson  in  Westchester  County. 

The  locality  as  listed  on  the  original  label  of  the  type  specimen  (U.S.N.M. 
Cat.  No.  193370,  collected  on  23  August  1884,  by  A.  K.  Fisher)  reads:  "Sing 
Sing,  N.Y."  and  on  the  back  is  written  "Merritts  Comers  4  miles  E  of  Sing  Sing." 
U.S.  Geological  Survey  maps  of  the  region  (,1893  edition,  reprinted  1897)  reveal 
that  Merritts  Corners,  the  type  locality  of  T.  s.  fisheri,  is  located  east  of  the 
Hudson  River,  in  AVestchester  County,  N.Y.,  at  41°11'27"  N  lat.,  and  73°47'51" 
W  long.,  and  is  approximately  3%  miles  E  and  1%  miles  N  of  Ossining,  N.Y. 

General  distribution. — Middle  Atlantic  States,  from  the  lower  Hudson  River 
Valley  in  New  York,  south  to  Virginia  and  West  Virginia. 


68  NORTH  AMERICAN  FAUNA  66 

Distribution  in  Maryland. — ^Uncommon  in  the  Eastern  Shore  and 
Western  Shore  sections ;  abundant  locally  in  the  Piedmont  and  Ridge 
and  Valley  sections.  In  the  Allegheny  Mountain  section  it  is  replaced 
by  the  subspecies  T.  s.  lysteri.  (see  fig.  26.) 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  1/1,  3/3,  =  20;  a 
small,  heavyset  ground  squirrel  with  dense,  moderately  fine  fur; 
pelage  marked  by  two  pale  and  three  dark  stripes  on  sides  of  face 
and  five  blackish  and  four  pale  stripes  extending  down  the  back; 
rump  rusty  in  coloration;  top  of  head  and  dark  facial  stripes  near 
russet,  light  facial  stripes  pale  buffy;  dark  stripes  on  back  nearly 
black  in  color,  paler  stripes  near  smoke-gray  shading  posteriorly  into 
russet;  center  or  inner  pale  stripe  is  the  broadest  and  always  gray  in 
coloration;  tail  moderately  long,  grayish  red  and  not  bushy.  This 
species  may  be  distinguished  from  any  other  in  Maryland  by  the 
striping  pattern  of  the  pelage. 

Measurements. — Four  adults  from  the  District  of  Columbia  have 
the  following  external  measurements:  Total  length  243.2  (234-255) ; 
tail  90.2  (83-99) ;  hind  foot  34.1  (33-35).  Cranial  measurements  of 
nine  adults  from  the  vicinity  of  Washington,  D.C.,  are  as  follows: 
Greatest  length  39.5  (38.9-40.3) ;  zygomatic  breadth  22.0  (21.3-22.8) ; 
postorbital  breadth  11.2  (10.6-12.2) ;  length  of  nasals  13.2  (12.5-14.0). 

Habitat  ami  habits. — The  chipmunk  is  largely  a  ground  dweller, 
only  rarely  climbing  trees.  It  prefers  to  live  on  wooded  hillsides  or 
mountain  slopes,  but  is  also  fond  of  stone  walls  and  rail  fences.  Though 
usually  favoring  dry  situations,  it  is  occasionally  found  in  moist  bot- 
tom land  woods.  It  spends  a  good  deal  of  time  in  burrows  which  it 
digs  beneath  a  rock,  stone  wall,  tree  roots,  or  a  building.  The  burrow 
is  sometimes  as  much  as  20  feet  in  length  and  1  to  3  feet  below  the  sur- 
face of  the  ground.  The  chipmunk  in  Maryland  remains  more  or  less 
active  during  the  winter.  All  summer  long,  and  especially  in  the 
autumn,  it  is  busily  engaged  in  storing  food,  primarily  seeds  and  nuts 
for  winter  use.  This  food  is  kept  in  a  "storeroom"  adjoining  the  rooms 
where  the  animal  is  spending  the  winter.  The  food  of  the  chipmunk 
consists  of  small  seeds,  berries,  fruits,  and  nuts,  and  occasionally  small 
birds,  mice,  snakes,  snails,  slug,  insects,  and  other  small  animal  life. 
Chipmunks  are  polyestrous  and  breed  from  March  onward.  The  num- 
ber of  young  is  three  to  five,  and  the  gestation  period  31  days.  Puberty 
is  reached  at  the  age  of  2i^  to  3  months. 

Specimens  examined. — Anjne  Aru/ndel  County:  Epping  Forest  (near 
Annapolis),  2.  Frederick  County:  Catoctin  State  Park,  1.  Harford 
County:  Fallston,  3.  Howard  County:  Long  Corner,  2.  Montgomery 
County:  Bethesda,  1;  Chevy  Chase,  2;  Dickerson,  1;  Rockville,  3; 
Takoma,  1 ;  Washington  Grove,  2;  Linden,  1.  Prinze  Georges  Coumiy: 
Laurel,  5.  Distinct  of  Col/wmhia:  42. 


MAMMALS  OF  MARYLAND  69 

Other  records  and  reports. — Baltimore  County:  Bare  Hills-Lake 
Roland  Area  (Bures,  1948,  p.  67) ;  Lock  Raven  (Kolb,  1938) ;  Patapsco 
State  Park  (Hampe,  1939,  p.  6).  Montgomery  Cownty:  Sligo;  Piney 
Branch;  Silver  Spring;  Sandy  Spring  (all  from  Bailey,  1896,  p.  95) ; 
Plummers  Island  (Goldman  and  Jackson,  1939,  p.  133) .  Prince  Georges 
County :  Patuxent  Research  Center  (Herman  and  Warbach,  1956,  p. 
87).  'Worcester  County:  near  Milbum  Landing  (Vagn  Flyger,  per- 
sonal communication,  22  June  1964) . 

Tamias  striatus  lysteri  (Richardson) 

Sciurus  {Tamias)  lysteri  Richardson,  Fauna  Boreali- Americana,  1: 
181,  pi.  15,  June  1829. 

Type  locality. — Penetanguishene,  Ontario. 

General  distribution. — Nova  Scotia,  New  Brunswick,  and  southeastern  Ontario, 
south  into  Connecticut  and  Pennsylvania  and  in  the  Appalachian  Mountains  to 
western  Maryland. 

Distribution  in  Maryland. — Occurs  in  the  higher  mountains  (above 
2,000  feet  altitude)  of  the  Allegheny  Mountain  section  where  it  is 
abundant. 

Distinguishing  characteristics. — This  subspecies  is  similar  to  T.  s. 
flsheri.,  but  has  paler  upper  parts,  especially  the  rump  and  the  median 
grayish  bands.  This  paler  coloration  is  most  marked  in  the  northern 


Tamias  striatus  fisheri 
0  Specimens  examined 
O  Specimens  reported 


Tamias  striatus    lysteri 

\C^ 

-38"- 

A    Specimens  examined 
A  Specimens  reported 

""S? 

-^  ^ 

?• 

1 

T  7* 

76° 

■f//Y 


FiQXJKE  26. — ^Distribution  of  Tamias  striatus  fisheri  and  T.  s.  lysteri. 


70  NORTH  AlviEBIOANi  FAUNA  66 

part  of  the  range  of  the  subspecies  in  the  vicinity  of  the  type  locality. 
Maryland  specimens  are  not  so  pale  as  typical  J/ysteri. 

Cranially  the  differences  between  the  two  subspecies  are  very  slight. 
T.  s.  lysteri  averages  somewhat  smaller,  and  has  relatively  longer  nasal 
bones. 

Measurements. — External  measurements  of  five  adults  and  cranial 
measurements  of  four  adults  from  Garrett  and  Allegany  Counties,  Md., 
are  as  follows:  Total  length  233.4  (220-247);  tail  87.8  (81-100); 
zygomatic  breadth  21.2  (19.9-22.2)  ;  postorbital  breadth  10.9  (10.5- 
11.2) ;  length  of  nasals  13.5  (12.7-14.0) . 

Habitat  and  habits. — Similar  to  T.  s.  -fisheri. 

Specimens  examined. — Allegany  Cownty:  Dans  Mountain  (4  miles 
northwest  of  Rawlings),  1.  Garrett  County:  Bittinger,  1;  Cunning- 
ham Swamp,  1  (Coll.  U.  Md.) ;  Finzel,  4;  Grantsville,  1;  Herrington 
Manor,  1. 

Other  records  arid  reports. — Allegany  County:  Accident  (Howell, 
1929,  p.  19). 

Remarks. — All  Maryland  specimens  assigned  to  this  subspecies 
represent  intergrades  between  T.  s.  lysteri  and  T.  s.  fisheri  in  colora- 
tion, size,  and  relative  length  of  nasals,  and  assigning  them  to  lysteri 
is  somewhat  arbitrary.  Specimens  from  Fallston,  Harford  County,  are 
also  intergrades  but  are  closer  to  fisheri  and  have  been  assigned  herein 
to  that  subspecies. 

WOODCHUCK 
Marmota  tnonax  tnonax  (Linnaeus) 

[Mu^']  monaas  Linnaeus,  Syst.  nat.,  ed.  10,  1 :  60,  1758. 

Type  locality. — ^Maryland. 

General  distribution. — Middle  eastern  United  States  from  Pennsylvania,  New 
Jersey,  Ohio,  Indiana,  Illinois,  Lower  Peninsula  of  Michigan,  and  Iowa,  south 
to  Arkansas  and  the  northern  parts  of  Alabama,  Georgia,  and  South  Carolina. 

Distribution  in  Maryland. — Abundant  in  all  sections  except  the 
Eastern  Shore,  where  it  has  until  lately  been  unknown.  There  is  recent 
evidence,  however,  that  the  species  is  extending  its  range  into  that 
section. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  2/1,  3/3,  =  22;  the 
heaviest  member  of  the  squirrel  family  found  within  the  State  (weight 
5  to  12  lbs.);  tail  short  and  somewhat  bushy;  fur  thick  and  coarse; 
coloration  above  grizzled  brown,  with  top  of  head,  face,  legs,  and 
tail  dark  brown  to  blackish  brown;  under  parts  lighter  in  coloration, 
and  pelage  not  so  thick;  incisor  teeth  white;  ears  short  and  rounded. 

The  large  size,  grizzled  brownish  coloration,  and  short  bushy  tail 
readily  distinguish  this  animal  from  any  other  rodent  in  Maryland. 


MAMMALS  OF  MARYLAND 


71 


7  9- 

1 

78* 

77 

■jy 

* 

\ 

75' 
-39°- 

-39«- 
-36*- 

SCALE 
O        lO      ZO      30MILES 

T 

^ 

'§lllM§k 

76° 

Maimota  monax  monax 
•    Specimens   examined 
O    Specimens    reported 

1 

4 
i 

M 

BOM 

FiGUBE  27. — Distribution  of  Marmota  monax  monax. 


Measurements. — Males  average  larger  than  females  in  overall  size. 
Two  adult  females,  one  from  Sparks,  Baltimore  County,  and  the  other 
from  Washington,  D.C.,  have  external  measurements  as  follows :  Total 
length  628,  615;  tail  157,  148;  hind  foot  88,  86.  Cranial  measurements 
of  three  adult  males  from  the  District  of  Columbia  and  nearby  Mary- 
land are  as  follows:  Condylobasal  length  102.6,  97.5,  95.7;  palatal 
length  59.3,  56.2,  55.3;  zygomatic  breadth  69.3,  65.8,  65.9;  least  inter- 
orbital  breadth  27.3,  25.9,  27.2;  maxillary  toothrow  21.7,  21.6,  22.0. 
Cranial  measurements  of  five  adult  females  average:  Condylobabal 
length  91.3  (89.0-94.2)  ;  palatal  length  53.5  (51.0-56.0) ;  zygomatic 
breadth  62.5  (59.6-64.8)  ;  least  interorbital  breadth  24.6  (23.3-26.3) ; 
maxillary  toothrow  21.1  (20.4-21.8). 

Habitat  and  habits. — This  is  primarily  a  forest  border  and  open  j&eld 
mammal,  seldom  found  in  heavy  dense  woods.  It  prefers  the  edges 
of  brushy  woodlands,  and  particularly  open  fields  along  streams. 
Woodchucks  are  found  along  poorly  cleared  fence  lines,  in  meadows, 
cow  pastures,  and  grainfields,  especially  where  rocky  outcroppings  or 
old  stumps  occur.  They  are  common  on  the  bluffs  that  line  the  Mary- 
land side  of  the  Potomac  River,  and  occur  in  great  numbers  in  the 
farming  country  of  Montgomery  and  Frederick  Counties.  Hampe 
(1939,  p.  6)  reports  that  they  are  very  abundant  throughout  the 
Patapsco  State  Park,  and  that  numerous  burrows  are  found  in  the  hill- 
sides along  the  river.  In  the  Bare  Hills-Lake  Roland  region  of  Balti- 


72  NORTH  AMERICAN  FAUNA  66 

more  County,  Bures  (1948,  p.  67)  found  that  they  were  not  very 
common,  their  range  being  limited  to  areas  of  cultivation  and  the  region 
between  the  deciduous  woods  and  the  marsh,  Woodchucks  abound  in 
Garrett  County,  particularly  in  the  vicinity  of  Deep  Creek  Lake. 

This  species  is  active  both  day  and  night  and  is  frequently  seen 
in  grassy  shoulders  and  rocky  outcroppings  that  border  Maryland 
highways.  On  many  occasions  it  falls  victim  to  modern  high-speed 
traffic  and  is  one  of  the  most  frequently  encountered  road-kills  in  the 
State. 

The  woodchuck  inhabits  an  extensive  burrow  which  sometimes  ex- 
tends to  a  depth  of  5  feet  and  may  be  some  30  feet  in  length.  The  burrow 
usually  has  several  entrances,  which  may  be  located  beneath  a  wall  or 
tree  stump.  Within  the  burrow,  there  is  usually  one  chamber  in  which 
a  bulky  grass  nest  is  situated.  In  this  chamber  the  female  gives  birth 
to  four  or  five  young  in  April  or  May  after  a  gestation  period  of  about 
4  weeks.  The  babies  remain  in  the  den  for  about  a  month,  after  which 
their  eyes  open,  and  they  become  completely  independent  of  the  mother 
by  early  July. 

Principal  food  of  the  woodchuck  consists  of  grasses  and  succulents 
such  as  clover,  alfalfa,  plaintain,  and  various  perennials,  in  addition 
to  beans,  peas,  corn,  and  apples;  seldom  does  the  woodchuck  consume 
flesh,  although  it  has  been  known  to  pursue  poultry  and  eat  insects  and 
snails.  During  the  summer  it  becomes  fat  on  these  foods,  and  early 
in  the  autumn  when  the  first  frost  is  on  the  ground  it  descends  into 
its  burrow  and  goes  into  hibernation.  It  usually  emerges  again  in 
late  February  or  early  March. 

Specimens  examined. — Baltimore  Comity:  Sparks,  1,  Homard 
County:  Simpson ville,  1.  Montgomery  Cownty:  Plummmers  Island, 
4;  Sandy  Spring,  1.  Prince  Georges  County:  Laurel,  5;  near  Wash- 
ington, D.C,  1.  Washington  County:  Hagerstown,  1.  District  of 
Colamhia:  6, 

Other  records  and  reports. — Allegany  Cownty :  Mount  Savage  (Coll. 
U.  Md.).  Baltimore  County:  Bare  Hills-Lake  Roland  area  (Bures, 
1948,  p.  67) ;  Lock  Raven  (Kolb,  1938) ;  Patapsco  State  Park  (Hampe, 
1939,  p.  6),  Garrett  County:  Cranesville  Pine  Swamp  (Mansueti,  1958, 
p,  83),  Kent  County:  Galena  (Allen,  1950,  p,  28),  Prince  Georges 
County:  Patuxent  Research  Center  (Grizzell,  1949,  p,  74).  Washing- 
ton County :  Sharpsburg,  1  mile  W  (personal  observation) . 

Remarks. — Allen  (1950,  p,  28)  says  that  the  Eastern  Shore  is  one 
of  those  regions  that  has  been  invaded  by  the  woodchuck  in  the  last 
50  years.  It  first  appeared  on  the  Prettyman  Farm  near  Galena  in 
Kent  County  around  1900,  Evidently  it  is  spreading  southward  around 
the  Chesapeake  Bay  from  Pennsylvania, 


MAMMALS  OF  MARYLAND 


73 


GRAY  SQUIRREL 

Sciurus  carolinensis  pennsylvanicus  Ord 

Sciurus  pennsylvanica  Ord,  in  [Guthrie],  a  new  geographical,  histori- 
cal and  commercial  grammar ;  .  .  .  ,  Philadelphia,  ed.  2,  2 :  292, 1815. 

Type  locality. — Pennsylvania,  west  of  the  Allegheny  Ridge. 

General  distribution. — From  southern  New  Brunswick,  Quebec,  and  Ontario, 
south  into  Virginia  and  in  the  Appalachians  to  Tennessee,  west  into  eastern 
Iowa  and  southern  Minnesota. 

Distribution  in  Maryland. — ^Abundant  in  all  sections  of  the  State. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  2/1,  3/3,  =  22;  size 
large;  tail  bushy  and  flattened;  coloration  variable  both  in  summer 
and  winter;  upper  parts  usually  yellowish  brown  in  summer,  with  a 
slightly  grayish  cast  to  the  sides  of  the  neck,  the  shoulders,  and 
thighs;  face  clay  colored  to  cinnamon  buff;  forelegs  gray  above,  hind 
legs  reddish;  tail  brown  at  base,  hairs  blackish  near  middle  and  tipped 
with  gray;  in  winter  pelage,  paler  and  more  grayish. 

A  melanistic  color  phase  occurs  frequently  in  this  species,  par- 
ticularly in  8.  c.  petwisylv aniens.  Albinistic  animals  are  also  often 
encountered. 

Measurements. — External  and  cranial  measurements  of  three  adult 
males  from  Cambridge,  Dorchester  County,  are  as  follows:  Total 
length  462,  486,  465;  tail  vertebrae  201,  216,  190;  hind  foot  64,  64,  61; 


79-                                                                  78* 

1                                                                         ' 

77* 

76° 

7\ 

p 

/////^^^^^''-/^        '^'      w///V///v 

P 

P 

-39«- 

SCALE                                                           ^"^ 
O        lO      20      30MILES 

1 

M 

T/nP\ 

-39°- 

Sciurus  carolinensis  pennsylvanicus 
•     Specimens   examined                                  J 

^^M 

W/////^ 

-38"- 

O     Specimens    reported 

■M 

% 

1                                                  1 

T7" 

1 

76" 

sow 

Figure  28. — Distribution  of  Sciurus  carolinensis  pennsylvanicus. 


74  NORTH  AMEBICAN  FAUNA  66 

greatest  length  of  skull  62.6,  62.4,  62.8 ;  zygomatic  breadth  33.4,  33.4, 
33.6;  least  interorbital  breadth  16.9,  19,2,  18.2;  length  of  maxillary 
toothrow  10.9, 11.6,  11.2. 

Habitat  and  habits. — ^This  is  a  squirrel  of  the  hardwood  and  mixed 
coniferous-hardwood  forests,  particularly  those  with  nut-bearing  trees 
and  bushy  undergrowth.  It  is  quite  common  in  the  parks  of  Washing- 
ton, D.C.,  particularly  Rock  Creek  Park.  Most  of  these  are  descended 
from  introduced  stock.  Bailey  (1923,  p.  108)  says: 

The  late  Dr.  William  L.  Ralph  purchased  many  gray  squirrels  and  liberated 
them  in  the  Smithsonian  grounds,  where  up  to  the  time  of  his  death  in  1907  he 
fed  and  cared  for  them  .  .  .  They  soon  became  common  in  the  Mall  .  .  .  and 
spread  to  the  White  House  grounds,  LaFayette  Square,  and  other  city  parks. 

Melanistics  squirrels  were  introduced  and  liberated  into  the  Na- 
tional Zoological  Park  and  are  still  frequently  seen  there.  Of  these, 
Bailey  (1923, p.  109)  says: 

The  first  shipment  of  10  (black  squirrels)  was  from  Rondeau  Provincial  Park, 
Morpeth,  Ontario,  18  May  1906 ;  and  these  squirrels  were  immediately  liberated 
in  the  northwestern  part  of  the  zoo  where  they  were  very  much  at  home.  They 
have  since  been  constanly  in  the  park,  especially  from  the  vicinity  of  the  great 
flight  cage  to  the  Klingle  Valley  and  they  have  spread  northward  to  Cleveland 
Park  and  nearly  to  Chevy  Chase. 

Five  of  the  31  skins  of  gray  squirrels  in  the  National  Museum  collec- 
tions from  the  District  of  Columbia  show  melanistic  tendencies. 

The  gray  squirrel  is  common  throughout  Maryland.  Hampe  (1939, 
p.  6)  says  that  it  is  the  most  common  squirrel  in  the  Patapsco  State 
Park  and  has  been  observed  in  the  Park  every  month  of  the  year; 
young  squirrels  are  numerous  there  after  the  first  of  July.  Bures 
(1948,  p.  67)  says  the  gray  squirrel  is  quite  common  in  the  Bare  Hills- 
Lake  Roland  area.  I  found  them  numerous  on  the  Delmarva  Penin- 
sula; in  southern  Maryland;  in  the  Piedmont  region,  particularly  in 
the  vicinity  of  Sugar  Loaf  Mountain;  and  in  the  mountains  of  the 
western  part  of  the  State.  Gray  squirrels  do  not  occur  on  Assateague 
Island,  but  I  have  seen  them  in  the  thickets  back  of  the  dunes  several 
miles  north  of  Ocean  City. 

The  gray  squirrel  is  most  at  home  in  trees  and  descends  to  the  ground 
only  when  necessary  to  obtain  food  and  bury  nuts.  It  does  not  hiber- 
nate, even  in  the  coldest  northern  portions  of  its  range.  This  squirrel 
is  diurnal  and  is  most  active  in  the  early  morning  and  late  afternoon. 

Its  bulky  nest  is  generally  constructed  in  an  enlarged  natural  cavity 
^f  an  old  oak  tree,  but  sometimes  an  outdoor  nest  of  firmly  woven 
leaves  is  constructed  among  the  branches  or  in  the  crotch  of  a  tree. 

Squirrels  mate  during  midwinter,  and  the  gestation  period  is  about 
40  days.  A  second  mating  usually  occurs  sometime  in  May  or  June. 
The  young  are  two  to  five  (generally  four)  in  number.  When  2  months 


MAMMALS  OF  MARYLAND  76 

of  age,  they  are  weaned,  but  remain  with  the  mother  until  she  has  her 
second  litter. 

The  gray  squirrel  is  generally  vegetarian  in  habits,  its  food  consisting 
of  many  kinds  of  nuts  (including  acorns),  seeds,  fruits,  buds,  fungi, 
inner  bark  of  certain  trees,  and  occasionally  corn  and  other  grains,  and 
fleshy  parts  of  plants.  Sometimes  it  eats  small  amounts  of  animal  food 
such  as  insects  or  an  occasional  bird's  egg  or  small  bird. 

Specimens  examined. — Allegany  County:  Mount  Savage,  1  (Coll. 
U.  Md.).  Anne  Arundel  County:  Priest  Bridge,  1.  Calvert  County: 
Little  Cove  Point  Area,  2;  Prince  Frederick,  1.  Charles  County: 
Marshall  Hall,  1 ;  Newport,  1 ;  Port  Tobacco,  2.  Dorchester  County: 
Cambridge,  3.  Garrett  County :  Friendsville,  1^4  mile  NW,  1  (Coll.  U. 
Md.)  ;  Grantsville,  2;  Meadow  Mountain,  1  (Coll.  U.  Md.).  Harford 
County :  Fallston,  5.  Montgomery  County :  Dickerson,  1 ;  Germantown, 
2;  Kensington,  1;  Takoma  Park,  2;  Woodside,  1.  Prince  Georges 
County:  Beltsville,  1;  Bladensburg,  2;  Branchville,  1;  College  Park, 
1;  Fort  Washington,  1;  Laurel,  22;  (Upper)  Marlboro,  2;  Muirkirk, 
1;  Oxon  Hill,  1;  Patuxent  Eiver  (fork),  2;  Piscataway  Creek,  2; 
Scagg's  Swamp,  1.  District  of  Columbia:  40. 

Other  records  and  reports. — Allegany  County :  South  end  of  Town 
Hill  Mountain  (personal  observation) .  Baltimore  City  (Flyger,  1960b, 
p.  366).  Baltimore  County:  Bare  Hills-Lake  Roland  area  (Bures, 
1948,  p.  67) ;  Loch  Raven  (Kolb,  1938)  ;  Patapsco  State  Park  (Hampe, 
1939,  p.  ^).  Frederick  County:  Thurmont  (Coll.  U.  Md.) ;  Sugar  Loaf 
Mountain  (personal  observation).  Garrett  County:  Keyser's  Ridge 
(Coll.  U.  Md.)  ;  Montgomery  County :  Plummers  Island  (iGoldman 
and  Jackson,  1939,  p.  133) .  Prince  Georges  County :  Aquasco  (Herman, 
and  Reilly,  1955,  p.  402).  Worcester  County :  Ocean  City,  2  miles  N 
(personal  observation). 

Remarks. — All  of  Maryland  was  formerly  included  within  the  range 
of  the  southern  subspecies  of  gray  squirrel,  Sciurus  carolinensis  caro- 
linensis  Gmelin  (see  Bangs,  1896,  p.  153,  and  Miller,  1924,  p.  223). 
Patton  (1939,  pp.  75-76),  however,  in  a  study  of  the  distribution  of 
the  gray  squirrel  in  Virginia,  concluded  that  S.  c.  carolinensis  occupies 
the  southern  half  of  the  Piedmont  Plateau  and  the  entire  Coastal  Plain 
region  in  that  State.  He  says  that  in  Virginia  the  area  of  intergradation 
between  S.  c.  carolinensis  and  S.  c.  leucotis  (=  pennsylvanicus)  lies 
along  a  line  drawn  from  central  King  George  County  to  southeastern 
Patrick  County,  and  he  assigned  a  specimen  from  Eastville,  on  the 
Virginia  portion  of  the  Delmarva  Peninsula,  to  /S.  c.  carolinensis.  This 
suggests  that,  although  most  of  Maryland  lies  within  the  range  of  /S.  c. 
pennsylvanicus,  the  southern  .portions  of  the  Western  Shore  and 
Eastern  Shore  sections  are  within  the  range  of  S.  c.  carolinensis,  and 
the  range  of  the  species  in  Maryland  has  been  mapped  in  this  way  by 


76  NORTH  AMERICAN  FAUNA  66 

Hall  and  Kelson  (1959,  p.  371).  However,  a  careful  comparison  of 
specimens  from  Calvert  and  Charles  Counties  in  the  Western  Shore 
Section  and  Cambridge  in  the  Eastern  Shore  section  with  specimens 
of  typical  pennsylvanicus  from  central  Pennsylvania  and  New  York 
show  that  they  differ  in  no  essential  respect  from  that  subspecies, 
whereas  they  are  considerably  larger  and  paler  than  typical  carolinen- 
sis.  I  have  also  examined  the  specimen  from  Eastville,  Va.,  assigned 
by  Patton  (1939)  to  caroUnensis,  and  consider  it  to  be  referable  to 
pennsylvanicus.  It  is  somewhat  darker  than  typical  pennsylv aniens^ 
but  can  be  matched  in  coloration  by  many  specimens  in  similar  prelage 
from  the  northern  portion  of  the  range  of  pennsylvanicus.  In  size 
it  is  indistinguishable  from  typical  pennsylvanicus  and  considerably 
larger  than  carolinensis.  Consequently,  all  of  Maryland  falls  within 
the  range  of  S.  c.  pennsylvanicus.,  and  this  range  extends  at  least  as 
far  south  as  Eastville  on  the  Virginia  portion  of  the  Delmarva  Penin- 
sula and  probably  as  far  as  the  tip  of  that  peninsula. 

FOX  SQUIRREL 
Sciurus  niger  Linnaeus 

[Sciuincs]  niger  Linnaeus,  Syst.  nat.  ed.  10,  1 :  64,  1758. 

This  is  our  largest  tree  squirrel  and  one  of  the  most  spectacular 
rodents  in  Maryland.  It  resembles  the  gray  squirrel  but  is  considerably 
bigger  and  heavier,  and  less  often  observed.  Mansueti  (1952,  p.  31) 
comments  that  a  ratio  of  40  grays  to  one  fox  squirrel  may  be  high,  but 
that  few  fox  squirrels  have  been  reported  in  recent  years  and  the 
species  appears  to  be  becoming  scarce  in  all  the  Atlantic  Coast  States. 

The  distribution  of  fox  squirrels  in  Maryland  has  been  reviewed 
by  Mansueti  (1952,  pp.  31-41),  and  most  of  the  following  is  based 
upon  his  records  or  records  cited  by  him. 

Two  subspecies  occur  within  Maryland.  They  are : 

Sciurus  niger  cinereus  Linnaeus 

[Sciurus']  cinereus  Linnaeus,  Syst.  nat.,  ed.  10, 1 :  64, 1758. 

/Sciurus  niger  hryanti  H.  H.  Bailey,  Bailey  Mus.  Libr.  Nat.  Hist., 

Newport  News,  Virginia,  Bull.  No.  1  [p.  1],  1  August  1920.  (Type 

locality :  Dorcester  County,  Md.) 

Type  locality. — Restricted  to  Cambridg^e,  Dorchester  County,  Maryland,  by 
Barkalow  (1956,  p.  13). 

General  distribution. — Formerly  from  Northampton  County  in  Virginia  to 
southeastern  Pennsylvania,  but  now  confined  to  the  Eastern  Shore  section  of 
Maryland.  It  has  been  listed  by  the  Department  of  the  Interior  as  an  endangered 
form. 

Distribution  in  Maryland. — Occurs  in  limited  numbers  in  Dor- 
chester, Queen  Annes,  Talbot,  Wicomico,  Somerset,  and  Worcester 


MAMMALS  OF  MARYLAND  77 

Counties.  The  present  center  of  population  appears  to  be  in  the  vicinity 
of  Blackwater  National  Wildlife  Refuge  where  it  is  still  common. 
(See  fig.  29.) 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  1/1,  3/3,  =  20; 
coloration  uniform  light  grizzled-gray  above  with  a  steel  blue  cast; 
belly  and  feet  white;  tail  with  a  pronounced  black  stripe  on  outer 
edges.  A  melanistic  form  occurs  in  which  the  belly  and  back  are 
blackish.  May  be  readily  distinguished  from  the  gray  squirrel,  which 
it  resembles  somewhat  in  coloration,  by  its  much  larger  size  and 
reduced  dentition. 

Measurements. — Five  adults  from  Dorchester  County  have  external 
measurements  as  follows:  Total  length  579  (560-605) ;  tail  273  (263- 
285);  hind  foot  77  (73-81).  Cranial  measurements  of  four  adults 
from  Dorchester  County  are:  Greatest  length  68.5  (67.7-69.8)  ;  zygo- 
matic breadth  38.8  (37.9-39.8)  ;  least  interorbital  breadth  20.8  (19.4^ 
22.3)  ;  length  of  maxillary  toothrow  11.9  (11.8-12.0). 

Habitat  and  habits. — This  subspecies  prefers  mature  forests  of 
mixed  hardwoods  and  conifers  in  which  mast-producing  trees  such 
as  oaks,  hickories,  and  pines  are  present.  It  is  particularly  partial  to 
old-growth  loblolly  pine  forests,  many  of  which,  however,  have  been 
cut  over  or  burned  through  forest  fires. 

This  squirrel  spends  much  time  on  the  ground  but  generally  doesn't 
stray  far  from  the  home  roost.  It  lies  close  to  the  body  of  a  tree  or 
limb,  seldom  leaping  from  tree  to  tree  as  does  the  gray  squirrel.  Nests, 
which  serve  as  home  during  summer  and  winter,  are  placed  near 
the  tips  of  branches  in  old  pines,  generally  from  30  to  50  feet  above 
the  ground.  Mating  may  occur  at  any  time  throughout  the  year,  but 
is  most  frequent  during  the  latter  part  of  February  or  early  March. 
Usually,  four  young  comprise  a  litter  and  are  born  in  April. 

Fox  squirrels  feed  more  on  the  ground  than  do  gray  squirrels.  Food 
consists  primarily  of  acorns,  hickory  nuts,  walnuts,  and  particularly 
the  seeds  of  loblolly  pine.  They  seldom,  if  ever,  cause  damage  to  corn 
or  other  domestic  crops. 

This  squirrel  has  become  greatly  reduced  in  numbers  and  has 
entirely  disappeared  from  some  areas  of  its  former  range.  One  of  these 
areas  is  the  northern  portion  of  the  Eastern  Shore  section ;  this  is  the 
area  where  this  subspecies  would  be  expected  to  intergrade  with 
Sciurus  niger  vulpinus,  the  form  inhabiting  the  Western  Shore  of 
Maryland. 

Specimens  examined. — Dorchester  County :  Airey  (near),  1;  Black- 
water  Refuge,  1;  Bucktown,  1;  Cambridge,  9.  Kent  County:  East 
Neck  Island,  3.  Eastern  Shore  (no  exact  locality),  3. 

Other  records  and  reports  (with  dates  of  capture  or  sighting  when 
available). — Dorchester    County:    Big    Blackwater    Section,    1932, 

336-897  O — 69 6 


78  NORTH  AMERICAN  FAUNA  66 

(Dozier  and  Hall,  1944,  p.  5) ;  Gibbs  Marsh,  between  Golden  Hill  and 
Church  Creek,  near  Blackwater  River  (Mansueti,  1952,  p.  33)  ;  Grif- 
fins Neck  (Dozier  and  Hall,  1944,  p.  10) ;  Milton  (Dozier  and  Hall, 
1944,  p.  10) ;  Salem  Woods,  14  Miles  from  Cambridge  on  road  to 
Salisbury,  1933,  (Dozier  and  Hall,  1944,  p.  5)  ;  Secretary  (Dozier  and 
Hall,  1944,  p.  10) ;  Taylors  Island,  1963,  (James  B.  Trefethen  in 
correspondence  to  Bureau  of  Sport  Fisheries  and  Wildlife,  12  Novem- 
ber 1964).  Queen  Annes  County:  Church  Hill  (near),  4  miles  below 
Chestertown,  1943,  (Dozier  and  Hall,  1944,  p.  3).  Somerset  County: 
Big  Swamp,  2  miles  E  of  Kings  Creek,  1922,  (Dozier  and  Hall,  1944, 
p.  3) ;  Westover,  due  west  of,  1940,  (Dozier  and  Hall,  1944,  p.  3) ; 
Loretto,  near,  1944,  (Dozier  and  Hall,  1944,  p.  3).  Talbot  County: 
Trappe,  near,  1948,  (Mansueti,  1952,  p.  33).  Worcester  County:  New- 
ark, 1951,  (Mansueti,  1952,  p.  33) ;  Pocomoke  City,  near,  (Dozier  and 
Hall,  1944,  p.  3). 

Sciurus  niger  vulpinus  Gmelin 

[Sciurus]  vulpinus  Gmelin,  Syst.  nat.,  ed.  13,  p.  147,  1788  (based  on 
specimens  from  the  eastern  United  States,  including  the  Blue 
Mountains  of  Pennsylvania) . 

General  distribution. — Formerly  occurred  from  central  New  York,  south 
through  south-central  Pennsylvania,  western  Maryland,  eastern  West  Virginia, 
western  Virginia,  and  in  the  Appalachian  Mountains  to  western  North  Carolina. 
Distribution  presently  reduced  to  south-central  Pennsylvania,  Maryland,  western 
Virginia,  and  eastern  West  Virginia. 

Distribution  in  Maryland. — Found  locally  in  heavily  forested  re- 
j^ions  in  the  Western  Shore,  Piedmont,  Ridge  and  Valley,  and  Alle- 
gheny Mountain  sections. 

Distinguishing  characteristics. — Similar  in  size  and  general  charac- 
teristics to  >iS'.  n.  cinereu^,  but  differs  in  coloration.  The  body  is  general- 
ly buffy  brown  above,  in  contrast  to  the  bluish  grizzled  gray  of  cin- 
ereus;  tail  grayish  white  above,  rufous  below;  feet  and  ears  rufous; 
top  of  head  more  blackish  than  the  back.  May  be  distinguished  from 
the  gray  squirrel  by  its  larger  size. 

Measurements. —  No  external  measurements  are  available  for  any  of 
the  Maryland  adults  in  the  National  Museum  collections.  Two  adults 
from  White  Sulphur  Springs,  West  Virginia,  which  are  typical  of 
this  subspecies  have  the  following  measurements:  Total  length  615, 
603 ;  tail  299,  298 ;  hind  foot  77,  79.  Four  Maryland  specimens  (two 
from  Laurel,  Prince  Georges  County ;  one  from  Priest  Bridge,  Anne 
Arundel  County;  and  one  from  North  Chesapeake  Beach,  Calvert 
County)  have  the  following  cranial  measurements:  Greatest  length 
67.7  (66.6-68.2) ;  zygomatic  breadth  38.6  (38.2-39.4) ;  least  interor- 


MAMMALS  OF  MARYLAND 


79 


SCALE 

O   lO  20 

30  MILES 

Saiums  niger 

ainereus 

•  Specimens 

exami  ned 

0  Specimens 

reported 

G  Type  loca 

i  ty 

Saiwms  niger 

vulpinus 

A  Specimens 

examined 

A  Specimens 

reported 

Figure  29. — Distribution  of  Sckirus  niger  dnereus  and  8.  n.  vulpirms. 


bital  breadth  20.3  (20.1-20.5) ;  length  of  maxillary  toothrow  11.9 
(11.0-12.3). 

Habitat  and  habits. — Not  much  has  been  published  concerning  the 
habitat  and  habits  of  this  subspecies.  It  is  said  to  prefer  open  deciduous 
woods,  wood  borders,  and  orchards,  but  as  noted  by  Bailey  (1923,  p. 
110)  it  is  skillful  in  keeping  out  of  sight.  Mansueti  (1952,  p.  35)  states 
that  the  subspecies  has  been  considerably  decimated  in  recent  years, 
and  the  remaining  fox  squirrels  are  strictly  local  in  distribution  and 
are  more  or  less  relic  populations  where  they  occur. 

Bailey  (1923,  p.  110)  reported  that  at  various  times  fox  squirrels 
were  released  in  the  National  Zoological  Park  in  Washington,  D.C. 
These  apparently  never  flourished,  since  none  have  been  observed  in 
the  park  in  years. 

Specimens  examined. — Allegany  County:  Between  Clarysville  and 
Red  Hill,  1  (Coll.  U.  M.di.).  Anne  Arundel  County:  Patuxent  River  at 
Priest  Bridge,  10.  Calvert  County:  North  Chesapeake  Beach,  1.  Gar- 
ret CouMty :  Friendsville,  1/4  mile  NW,  2  (Coll.  U.  Md.).  Harford 
County:  Fallston,  1.  Prince  Georges  County:  Laurel,  4.  District  of 
Columbia:  4  (these  were  either  purchased  at  the  Central  Market  or 
trapped  in  the  National  Zoological  Park,  and  probably  are  not  actually 
from  the  District  of  Columbia  area) . 

Other  records  wnd  reports  (from  Mansueti,  1952,  except  where 
otherwise  noted. — Allegany  County :  Green  Ridge  State  Forest,  1935. 


80  NORTH  AMERICAN  FAUNA  66 

Calvert  County:  Governors  Run,  1948  ( ?).  Garrett  County:  Accident 
1945  and  1951 ;  Bittin^er,  1948 ;  Meadow  Mountain,  1947.  Montgomery 
County:  Great  Falls,  1916;  Plummers  Island  (Goldman  and  Jackson, 
1939,  p.  133).  Prinx:e  Georges  County:  Bladensbur^  (near),  1949  ( ?). 
College  Park,  1948 ;  1/2  mile  east  of  intersection  of  Hig;liways  214  and 
301,  1940.  WasJiington  County:  Fort  Frederick  State  Park,  1950. 

Remarks. — Mansueti  (1952,  p.  35)  lists  on  a  provisional  basis  a 
third  subspecies  of  the  fox  squirrel  in  Maryland,  the*  more  western 
Sciurus  n.  ruflventer.  He  and  Vagn  Flyger  in  1950  examined  the  tail 
of  a  fox  squirrel  shot  on  a  hill  near  Storey's  Landing,  Deep  Creek 
Lake,  Garrett  County,  several  years  before,  and  found  that  its  colora- 
tion was  similar  to  that  of  ruflventer.  This  subspecies  normally  occurs 
west  of  the  Allegheny  Mountains  and  prefers  open  or  parklike  upland 
woods  rather  than  heavily  forested  sections.  It  commonly  occurs  along 
fence  rows  in  cultivated  fields  or  in  pastures  where  there  are  only  scat- 
tered trees,  Mansueti  claims  that  these  conditions  are  found  in  many 
parts  of  Garrett  County,  particularly  around  Deep  Creek  Lake  and 
that  ru-flventer  may  be  moving  into  this  area  from  further  west.  He 
states  that  possibly  as  the  heavily  forested  areas  are  cut,  and  S.  n. 
vulpinu^  vacates,  S.  n.  ru^venter  invades  the  area  vacated.  On  the 
other  hand,  he  notes  that  numbers  of  S.  n.  ruflventer  have  been  re- 
leased in  southwestern  Pennsylvania  in  an  effort  to  restock  the  area 
and  some  of  these  may  have  migrated  south  into  Maryland.  The  two 
specimens  from  Garrett  County  that  I  have  examined,  however,  are 
typical  S.  n.  vulpinus  and  exhibit  none  of  the  characters  of  I'ufiventer. 

RED  SQUIRREL 

Tamiasciurus  hudsonicus  loquax  (Bangs) 

Sciurus  hudsonicus  loquax  Bangs,  Proc.  Biol.  Soc.  Washington,  10: 
161,  28  December  1896. 
Type  locality. — Liberty  Hill,  Conn. 

General  distribution. — Southern  Ontario,  southern  Vermont  and  New  Hamp- 
shire, south  to  northern  Virginia  and  "West  Virginia,  west  to  eastern  Iowa  and 
southeastern  Minnesota. 

Distribution  in  Maryland. — Occurs  locally  in  the  Piedmont,  Ridge 
and  Valley,  and  Allegheny  Mountain  sections;  scarce  or  absent  over 
most  of  the  Western  Shore  section ;  apparently  absent  in  the  Eastern 
Shore  section. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  2/1,  3/3,  =  22; 
anterior  upper  premolar  frequently  lacking,  and  when  present  so 
reduced  as  to  be  easily  overlooked;  size  small,  the  smallest  of  our 
local  tree  squirrels;  tail  relatively  short  and  bushy;  general  coloration 
in  winter  bright  rufous  above,  white  below;  ears  tufted  with  black; 
in  summer,  coloration  more  olive  dorsaUy,  \vith  ears  untufted. 


MAMMALS  OF  MARYLAND 


81 


^/t 


m 

U  MmJ 

* 

S  W  f\ 

-39«- 

SCALE 
O        lO      ZO      30MILES 

mI™ 

11 

fd£r'\(\ 

\Jtl       rJ 

j)^  r^jy    y 

yj  j       h 

i 

to^/rY^   1       \ 

^^IJ  j  I j  11 

h 

7t  *>•  l!  'Vs    S^'T" 

Tamiasciurus  hudsonious   loquax 

mNiM 

1 J 

9    Specimens   examined 

V 

H  wHiiJlfi 

^ 

O    Specimens    reported 

^ 

-^ 

-38*- 

1                                                     1 

79*                                                            78* 

TT" 

1 

76' 

'T 


"T^ 


Figure  30. — Distribution  of  Tamiasciurus  hudsonicus  loquax. 


This  squirrel  is  differentiated  from  all  others  in  Maryland  by  its 
small  size  and  reddish  coloration. 

Measurements. — Two  adults  from  the  vicinity  of  Bethesda,  Mont- 
gomery County,  have  external  measurements  as  follows :  Total  length 
310,  303;  tail  130,  130;  hind  foot  50,  51;  ear  22,  27.  Cranial  measure- 
ments of  10  adults  from  Laurel,  Prince  Georges  County  are :  Greatest 
length  45.2  (44.4-46.0) ;  zygomatic  breadth  26.2  (26.0-27.2) ;  least 
interorbital  breadth  13.9  (13.1-14.6) ;  length  of  maxillary  toothrow 
7.2  (6.6-7.8). 

Habitat  and  liahits. — This  squirrel  prefers  spruce  and  hemlpck 
forests,  but  is  often  found  in  deciduous  woods  and  in  rural  areas  in 
the  northern  hardwoods  region  where  it  sometimes  builds  nests  in 
the  attics  of  houses.  It  is  more  terrestrial  than  the  gray  squirrel,  spend- 
ing a  great  deal  of  time  on  the  ground  searching  for  food.  It  is  also 
more  omnivorous  than  the  gray  squirrel,  eating  almost  any  kind  of 
seed,  nut,  or  berry.  Various  kinds  of  fungi  are  consumed  and  even 
an  occasional  ^gg  when  the  nest  of  a  songbird  is  raided.  Hamilton 
(1943,  p.  224)  says  that  it  has  been  known  to  Ivill  and  partially 
devour  young  cottontail  rabbits. 

The  bulky  nest  of  the  red  squirrel,  made  of  grass  and  moss,  is 
usually  placed  high  in  the  branches  of  a  tree  and  can  be  distinguished 
from  that  of  the  gray  squirrel  by  its  smaller  size  and  the  finer  material 
used  in  its  construction.  The  red  squirrel  is  active  throughout  the  year. 


82  NORTH  AMERICAN  FAUNA  66 

It  produces  litters  of  from  three  to  six  young  early  in  the  spring  and 
often  a  second  litter  in  late  summer. 

The  center  of  Maryland's  red  squirrel  population  is  the  spruce  and 
hemlock  forests  of  the  Allegheny  Mountain  section  of  the  State.  It  is 
scarce  or  absent  over  most  of  the  Western  Shore  section  and  apparently 
lacking  in  the  Eastern  Shore  section.  David  H.  Johnson,  formerly 
Curator  of  Mammals,  U.S.  National  Museum,  tells  me  that  he  is  very 
familiar  with  pine  woods  near  Greenbelt,  Prince  Georges  County,  and 
never  observed  a  red  squirrel  there.  J.  C.  Lingebach,  Division  of  Mam- 
mals, U.S.  National  Museum,  advises  me  that  in  his  many  years  of  field 
experience  in  the  Annapolis  area  of  Anne  Arundel  County  he  never 
observed  a  red  squirrel.  Flyger  (1957,  p.  1),  however,  reports  that 
he  trapped  a  red  squirrel  on  23  February  1957  near  the  Naval  Academy 
in  Annapolis  and  that  there  had  been  a  colony  there  for  several 
years.  This  is  probably  an  artificially  introduced  population.  Red 
squirrels  have,  however,  been  taken  at  such  Western  Shore  section 
localities  as  Laurel,  Bladensburg,  Oxon  Hill,  Riverdale,  and  College 
Park,  in  Prince  Georges  County,  and  Marshall  Hall  in  Charles  County. 
These  localities  are  not  very  distant  from  the  fall  line  and  the  begin- 
ning of  the  Piedmont  section,  and  elsewhere  in  the  Western  Shore 
section  the  red  squirrel  appears  to  be  exceedingly  scarce. 

Even  in  the  Piedmont  section  the  species  is  only  locally  abundant, 
being  completely  absent  over  large  areas.  At  one  time  it  was  numerous 
in  Rock  Creek  Park  in  Washington,  D.C.,  but  none  have  been  seen 
there  in  recent  years.  It  is  still  plentiful  in  some  suburban  areas  north- 
west of  Washington.  A  lactating  female  was  found  dead  by  David 
H.  Johnson  on  a  road  adjacent  to  a  pine  woods  a  few  miles  northwest 
of  Bethesda,  Montgomery  County,  in  October  1955,  and  another  near 
this  general  area  in  September  1957.  Johnson  tells  me  that  it  is  the 
common  squirrel  in  some  of  the  pine  woods  in  the  Bethesda  area, 
being  more  often  seen  there  than  gray  squirrels.  In  the  Piedmont  sec- 
tion of  Baltimore  County,  Hampe  (1939,  p.  6)  reported  red  squirrels 
uncommon  in  the  pine  woods  of  the  Patapsco  State  Park,  but  Bures 
(1948,  p.  67)  found  that  it  was  a  common  resident  of  the  Bare  Hills- 
Lake  Roland  area  a  few  miles  to  the  northeast.  Evidently,  the  red 
squirrel  has  a  scattered  distribution  in  Maryland  and  is  only  abundant 
locally. 

Specimens  examined. — Allegany  County:  Frostburg,  1;  Mount 
Savage,  2  (Coll.  IT.  Md.).  Charles  County:  Marshall  Hall,  1.  Frederich 
County:  Middletown,  6.  Garrett  County:  Bittinger,  1;  Finzel,  2; 
Grantsville,  1 ;  Swallow  Falls  State  Park,  1.  Harford  County:  Falls- 
ton,  1.  Hoioard  County:  Long  Corner,  1.  Montgomery  County:  Be- 
thesda, 31/2  miles  NW,  1 ;  Bethesda,  5  miles  NW,  1 ;  Kensington,  8 ; 
Linden,  2;  Plummers  Island,  1;  Takoma  Park,  3.  Prince  Georges 


MAMMALS  OF  MARYLAND  83 

County:  Bladensburg,  2;  College  Park  (near),  1;  Laurel,  16;  Oxon 
Hill,  1 ;  Eiverdale,  1.  District  of  Columbia:  25. 

Other  records  and  reports. — Allegany  County:  Dans  Mountain 
(Coll.  U.  Md.) .  Anne  Arundel  County :  Annapolis  (Flyger,  1957,  p.  1) . 
Baltimore  County:  Bare  Hills-Lake  Roland  area  (Bures,  1948,  p.  67) ; 
Loch  Raven  (Kolb,  1938) ;  Patapsco  State  Park  (Hampe,  1939,  p.  6). 
Cecil  County:  Northeast  (Coll.  Acad.  Nat.  Sci.  Philadelphia).  Mont- 
gomery County:  Silver  Spring  (files  of  U.S.  Fish  and  Wildlife  Serv- 
ice). Prince  Georges  County :  Hyattsville  (Bailey,  1923,  p.  107). 

Remarks. — Specimens  from  Garrett  County  and  Allegany  County 
appear  somewhat  darker  in  summer  and  winter  pelage  than  specimens 
from  farther  east  in  the  State  and  may  represent  intergrades  with  the 
southern  Appalachian  subspecies  T.  h.  abieticola. 

SOUTHERN  FLYING  SQUIRREL 
Glaucomys  volans  volans  (Linnaeus) 

[Mus]  volans  Linnaeus,  Syst.  Nat.,  ed.  10,  1 :  63,  1758. 

Type  locality. — Virginia  (fixed  by  Elliot,  Field  Columb.  Mus.,  Zool.  Ser.,  2: 
109,  1901). 

General  distribution. — From  central  Minnesota,  Upper  and  Lower  Peninsulas 
of  Michigan,  southeastern  Ontario,  New  York,  and  southern  New  Hampshire, 
south  to  North  Carolina  and  Tennessee,  west  to  eastern  Kansas  and  Nebraska. 

Distribution  in  Maryland. — Probably  abundant  in  all  sections  of 
the  State  where  there  is  suitable  habitat.  No  specimens  or  records  are 
available,  however,  from  the  Eastern  Shore,  Ridge  and  Valley,  and 
Allegheny  Mountain  sections,  but  this  probably  indicates  that  these 
sections  have  not  been  systematically  trapped  for  the  species  rather 
than  a  scarcity  of  the  animals  themselves.  Flying  squirrels  are  noc- 
turnal, shy,  and  seldom  observed. 

Distinguishing  characteristics. — Teeth  l/.l,  0/0,  2/1,  3/3,  =  22;  a  small 
squirrel  that  is  characterized  by  a  "flying  membrane",  a  loose  fold  of 
fully  furred  skin  connecting  the  fore  and  hind  limbs  from  wrists  to 
ankles.  The  tail  is  broad,  flattened,  and  almost  paraUel-sided,  with 
the  tip  rounded;  pelage  extremely  soft  and  dense;  coloration  of  upper 
parts  varies  with  season  and  age,  but  is  generally  grayish  brown; 
under  parts  ususally  white  or  creamy  white  in  coloration,  with  the 
white  extending  from  the  base  of  the  hairs  to  the  tip;  dark  brown 
streak  extending  along  side  edge  of  "flying  membrane";  tail  grayish 
above,  cinnamon  below;  forefeet  white,  hind  feet  brown  except  for 
some  white  on  toes. 

This  species  may  be  distinguished  from  all  other  squirrels  in  Mary- 
land by  the  distinctive  "flying  membrane."  The  northern  flying  squir- 
rel, Glaucomys  sabrinus,  has  not  as  yet  been  reported  from  Maryland, 


84 


NORTH  AMERICAN  FAUNA  66 


Glaucomys  volans  volans 
#  Specimens  examined 
O  Specimens  reported 


Figure  31. — Distribution  of  Glaucmnys  volans  volans. 

but  may  occur  in  spruce  and  fir  forests  in  the  highest  elevations  of  the 
Allegheny  Mountain  section.  It  differs  from  the  present  species  pri- 
marily in  that  it  is  much  larger  in  size  and  the  basal  portion  of  the 
white  hairs  of  the  belly  are  colored  grayish. 

Measurements. — External  and  cranial  measurements  of  eight  adults 
from  Newport,  Charles  County,  are  as  follows:  Total  length  221.9 
(211-240)  ;  tail  vertebrae  97.9  (90-110) ;  hind  foot  26.6  (21-30)  ;  great- 
est length  of  skull  34.6  (33.5-35.6) ;  zygomatic  breadth  20.5  (19.7- 
21.3) ;  interorbital  breadth  6.9  (6.5-7.5) ;  length  of  maxillary  tooth 
row  6.4  (6.2-6.5). 

Habitat  and  hahits.— This  is  essentially  a  species  of  the  heavy  timber 
and  is  never  found  at  any  great  distance  from  water.  It  prefers  forests 
of  deciduous  trees,  but  is  sometimes  encountered  in  woodlands  of  mixed 
conifers  and  hardwoods.  Occasionally  it  may  occupy  an  old  orchard. 

The  species  is  probably  abundant  in  all  sections  of  the  State  where 
there  is  suitable  habitat,  but  because  of  its  secretive  habits  it  is  seldom 
noticed.  Bures  (1948,  p.  67)  says  that  in  the  Bare  Hills-Lake  Roland 
area  of  Baltimore  County  it  is  as  common  as  the  chipmunk,  but  because 
of  its  nocturnal  habits  is  less  often  observed.  Hampe  (1939,  p.  6)  found 
that  it  was  fairly  common  in  the  Patapsco  State  Park.  He  observed  one 
at  twilight  on  22  May  1936.  Bailey  (1923,  p.  112)  found  the  species 
common  in  the  woods  of  the  District  of  Cx)lumbia,  right  up  to  the  edge 
of  the  city. 


MAMMALS  OF  MARTLANI>  85 

Tlie  flying  squirrel  is  one  of  the  most  nocturnal  mammals  in  Mary- 
land, rarely  leaving  its  nest  before  the  sun  is  well  down.  lit  remains 
active  throughout  the  night,  foraging  for  hickory  nuts,  beechnuts, 
acorns,  maple  and  wild  cherry  seeds,  apples,  and  buds  and  blossoms  of 
some  trees.  It  is  carnivorous  to  some  extent  and  occasionally  feeds  on 
insects,  young  birds,  and  birds'  eggs.  This  squirrel  is  highly  social. 

The  favorite  nesting  site  for  the  flying  squirrel  is  a  hole  in  a  dead  or 
dying  tree.  A  cavity  made  by  a  woodpecker  is  often  preferred,  although 
occasionally  a  natural  one  will  be  utilized  and  artificial  bird  nest  boxes 
are  sometimes  used.  The  nest  is  composed  of  finely  shredded  leaves  and 
inner  bark. 

This  species  probably  does  not  hibernate  in  Maryland,  although 
farther  north  it  becomes  inactive  during  colder  weather  (Sollberger, 
1940,  p.  285).  Mating  may  occur  in  late  February  or  early  March  and 
the  gestation  period  is  about  40  days.  Three  young  usually  comprise  a 
litter,  and  a  second  mating  sometimes  occurs  in  July  ( Sollberger,  1943, 
p.  163). 

Specimens  examined. — Anne  Arundel  County:  Annapolis,  3  miles 
NW,  1.  Charles  County:  Marshall  Hall,  2;  Newport.,  10.  Montgomery 
County :  Cabin  John  Creek,  1 ;  Capitol  View,  1 ;  Chevy  Chase,  1 ;  Dick- 
erson,  1 ;  Garrett  Park,  1 ;  Glen  Echo  Heights,  1 ;  Great  Falls,  1 ;  Kens- 
ington, 2;  Plummers  Island  (near),  1;  Silver  Spring,  4.  Prince 
Georges  County:  Anacostia  Eiver,  NW  Branch,  1;  Branchville,  1; 
Laurel,  2 ;  Upper  Marlboro,  1 ;  no  exact  locality,  3.  St.  Ma^^s  County: 
Tall  Timbers,  1. 

Other  records  and  reports. — Allegany  County:  Mount  Savage 
(Coll.  U.  Md.)  ;  Town  Hill  (Coll.  U.  Md.).  Baltimore  County:  Bare 
Hills-Lake  Roland  area  (Bures,  1948,  p.  67) ;  Patapsco  State  Park 
(Hampe,  1939,  p.  6).  Cecil  County:  Bacon  Hill  (3  specimens  m  Phila. 
Acad.  Nat.  Sci.).  Montgomery  County:  Forest  Glen  (Bangs,  1896, 
p.  166).  Prince  Georges  County:  Patuxent  Research  Center  (Herman 
and  Warbach,  1956,  p.  87) . 

Family  CASTORIDAE  (beavers) 

BEAVER 

Castor  canadensis  Kuhl 

Castor  canadensis  Kuhl,  Beitr.  z.  zool.  u.  vergleich.  Anat.,  Ablth.  1, 
p.  64,  1820. 

Type  locality. — Hudson  Bay. 

General  distribution. — Formerly  ranged  over  most  of  the  forested  regions  of 
North  America,  north  of  Mexico.  It  was  exterminated  in  many  areas  of  its  range 
and  later  successfully  reintroduced  into  some  sections. 


86  NORTH  AMERICAN  FAUNA  66 

Distribution  in  Maryland. — Formerly  occurred  in  all  sections  of  the 
State,  but  was  exterminated  around  the  turn  of  the  century  or  earlier. 
It  has  been  deliberately  restocked  in  some  areas  and  naturally  invaded 
others  from  neighboring  States  where  animals  were  stocked  or  rem- 
nant populations  survived. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  1/1,  3/3,  =  20; 
largest  rodent  in  Maryland;  body  thickset  and  compact;  legs  short; 
ears  small;  hind  feet  large  with  the  toes  webbed;  tail  broad,  flat, 
nearly  hairless,  and  covered  with  large  scales;  pelage  with  very  soft 
dense  underfur,  overlaid  vnth.  long  coarse  guard  hairs;  coloration  dark 
rich  brown  above,  lighter  below. 

Measurements. — "Nine  adults  from  the  Allegheny  National  Forest, 
Pennsylvania,  average:  Total  length,  1,031  mm.  (970-1,090  mm.); 
tail  vertebrae,  358  mm.  (260--i40  mm.) ;  greatest  width  of  tail,  129 
mm.  (112-150  mm.)  ;  hind  foot,  169  mm.  (156-183.)."  (Handley  and 
Patton,1947,p.l58). 

"The  skull  is  large  and  massive,  that  of  the  adult  more  than  120  mni. 
long  and  85  mm.  broad;  .  .  .  length  of  upper  molar  series  about  28 
to  30  mm."  (Jackson,  1961,  p.  192) . 

Habitat  and  habits. — This  species  prefers  forested  areas  wherever 
there  are  suitable  watercourses  for  the,  construction  of  dams  and 
lodges.  The  sluggish  fresh- water  streams  of  the  Eastern  Shore  section 
are  especially  suited  to  their  needs. 

The  beaver  feeds  on  a  wide  range  of  plants.  These  may  be  sedges, 
rushes,  water  grasses,  various  roots  and  tubers,  and  bark,  leaves,  and 
twigs  of  bushes  and  trees.  In  winter  it  feeds  primarily  on  green 
branches  that  it  stores  under  water  near  the  lodge.  In  Maryland  its 
favorite  trees  appear  to  be  sweetgum,  pine,  ash,  dogwood,  oak,  and 
maple. 

These  animals  are  monogamous,  and  it  is  believed  that  they  mate 
for  life.  Breeding  begins  about  mid- January  and  extends  to  the  end  of 
February.  The  gestation  period  is  approximately  120  days,  and  a 
single  litter  of  from  one  to  eight  kits  is  produced  a  year  (the  most 
frequent  number  being  four  or  five). 

The  beaver's  most  important  activity  is  felling  trees  for  dams  and 
lodges.  A  large  beaver  lodge  is  about  5  to  6  feet  high  and  15  or  20  feet 
wide  at  the  water  level.  More  often,  however,  smaller  lodges  are  built, 
some  3  to  4  feet  in  height  and  8  to  10  feet  in  diameter.  The  inside  of 
a  lodge  consists  of  one  room  about  2  to  3  feet  in  height,  and  as  many 
as  8  to  10  beaver  may  occupy  it.  The  opening  to  the  lodge  is  always 
under  water.  Many  beavers,  however,  that  inhabit  lakes  or  deep 
streams  live  in  bank  dens  rather  than  constructing  lodges  and  dams. 

The  beaver  is  active  throughout  the  year,  but  is  seldom  active  during 
daylight  hours.  Its  routine  workday  begins  at  dusk  and  ends  at  dawn. 


MAMMALS  OF  MARYLAND  87 

Young  beavers  in  their  second  year  leave  the  parental  colonies  and 
emigrate  to  establish  themselves  in  new  colonies  by  pairs.  Sometimes 
they  may  move  as  much  as  30  miles  to  a  new  home.  Most  of  tliis 
movement  is  accomplished  in  the  water,  because  the  animal  is  quite 
clumsy  and  slow  moving  on  land. 

According  to  Mansueti  (1950,  p.  33)  no  one  knows  when  Maryland's 
native  beavers  were  finally  exterminated.  He  judges  that  on  the  basis 
of  when  they  disappeared  in  Pennsylvania  and  New  Jersey,  they  prob- 
ably were  gone  from  the  Maryland  lowlands  about  150  years  ago 
and  that  there  were  probably  some  native  beavers  left  in  western 
Maryland  less  than  100  years  ago.  Their  extirpation  was  due  to  a 
number  of  reasons,  the  primary  ones  being  heavy  trapping  pressure 
for  their  pelts,  and  elimination  of  suitable  habitat.  Beaver  have  reap- 
peared in  Maryland  in  recent  years  either  through  deliberate  intro- 
ductions or  as  a  result  of  their  natural  migrations  from  other  states 
where  they  had  not  been  entirely  extirpated  or  had  been  stocked. 
They  are  flourishing  now  in  certain  areas,  presumably  because  low 
pelt  value  makes  trapping  unprofitable  in  the  State. 

Recent  records  and  reports. — Bonwill  and  Owens  (1939,  pp.  36-37) 
mention  3  areas  of  Maryland  where  these  animals  were  thriving  in 
1939.  One  was  on  the  Upper  Potomac  River  near  Gormania,  Garrett 
County ;  the  second  on  Town  Creek  in  Allegany  County ;  and  the  third 
at  a  point  where  the  Andover  and  Sewell  Creeks  meet  at  the  head  of 
the  Chester  River  in  Kent  County.  They  believe  that  the  first  two 
colonies  were  the  result  of  migrations  from  colonies  in  Pennsylvania 
or  West  Virginia  that  had  escaped  extermination  in  those  States  or 
had  been  reintroduced  there.  The  Kent  County  colony  was  a  result  of 
migration  from  a  colony  in  Delaware  which  had  been  stocked  with 
animals  from  Maine  by  the  Delaw^are  Board  of  Game  and  Fish  Com- 
missioners in  1935. 

Amer  (1949,  p.  23)  says  that  the  beaver  migrated  into  the  western 
Maryland  Counties  of  Garrett  and  Allegany  from  colonies  in  West 
Virginia  and  are  firmly  established  in  eight  streams  in  Garrett  County 
and  three  streams  in  Allegany.  They  may  be  found  in  Garrett  County 
in  the  Youghiogheny  River,  Laurel  Run,  Harrington  Creek,  and 
Broad  Ford  Run.  In  Allegany  County  they  inhabit  Evitts  Creek  and 
Town  Creek;  and  beaver  cuttings  have  been  found  on  Sideling  Hill 
in  Washington  County.  He  estimates  that  in  1949  there  were  150 
beavers  in  western  Maryland. 

Remarks. — Authorities  are  in  agreement  that  Maryland's  native 
beaver  population  probably  represented  the  subspecies  C.  c.  cana- 
densis. It  is  impossible  to  assign  subspecific  rank  to  Maryland's  present 
beaver  population  since  they  come  from  so  many  different  sources, 
and  even  some  of  the  areas  from  which  they  have  been  stocked  were 


88  NORTH  AMERICANi  FAUNA  66 

themselves  stocked  at  an  earlier  period  with  animals  from  elsewhere. 
No  specimens  of  the  native  population  or  the  present  population  of 
beavers  have  been  available  to  me  for  examination. 

Family  CRICETIDAE  (deer  mice,  harvest  mice,  voles,  etc.) 

MARSH  RICE  RAT 
Oryzomys  palustris  palustris  (Harlan) 

Mus  palustris  Harlan,  Silliman's  Amer.  Jour.  Sci.,  31 :  385, 1837. 

Type  locality. — "Fast  Land"  near  Salem,  Salem  County.  N.J. 

General  distribution.— In  the  Coastal  Plain  from  southeastern  Pennsylvania 
and  southern  New  Jersey,  south  to  northern  Florida,  west  to  the  Mississippi 
River  and  north  in  the  Mississippi  Valley  to  southeastern  Missoiiri,  southern 
Illinois,  and  central  Kentucky. 

Distribution  in  Maryland. — Recorded  only  from  the  Eastern  Shore 
and  Western  Shore  sections. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  0/0,  3/3,  =  16;  ratlike 
in  general  appearance,  but  considerably  smaller  than  adult  Norway 
rat;  tail  long,  nearly  half  the  total  length;  fur  long  and  coarse;  color  of 
upper  parts  grizzled  grayish  brown,  mixed  with  blackish,  sides  paler 
with  less  blackish;  underparts  white  to  pale  buff;  tail  sparsely  haired 
and  scaly,  brownish  above  and  whitish  below.  Young  animals  are 
more  grayish  than  adults. 


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0     Specimens    examined 
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FiGUKE  32. — Distribution  of  Oryzomys  palustris  palustris. 


MAMMALS  OF  MARYLAND  89 

Marsh  rice  rats  superficially  resemble  young  Norway  rats  from 
which  they  may  be  distinguished  by  the  upper  cheek  teeth.  These  teeth 
have  two  longitudinal  rows  of  tubercles  in  rice  rats;  in  Norway  rats 
there  are  three  such  rows. 

Measurements. — An  average-sized  female  from  West  Ocean  City, 
Worcester  County,  has  measurements  as  follows:  Total  length  247; 
tail  120 ;  hind  foot  30 ;  ear  10 ;  greatest  length  of  skull  30.4 ;  zygomatic 
breadth  16.4 ;  interorbital  breadth  4.9 ;  length  of  upper  molar  toothrow 
4.4. 

An  adult  female  from  Nanjemoy  Creek,  Charles  County,  has  the 
following  external  measurements:  Total  length  262;  tail  127;  hind 
foot  30. 

There  is  a  peculiar  size  variation  often  encountered  in  this  species. 
Males  and  females  generally  average  about  the  same  size,  but  often 
an  apparently  adult  female  may  be  strikingly  smaller  than  the  average. 

Habitat  and  habits. — ^^This  species  is  partially  amphibious  and  shows 
a  great  preference  for  wet  meadows,  marshy  areas,  watercourses,  cane 
breaks,  and  swamps,  and  is  only  rarely  encountered  in  dry  fields. 

Marsh  rice  rats  are  polyestrous  and  breed  from  March  to  November 
in  Maryland  (Harris,  1953,  p.  485).  The  gestation  period  is  25  days 
and  the  female  mates  again  immediately  after  parturition.  Litter  size 
varies  from  one  to  five  with  the  average  being  three. 

This  species  is  an  accomplished  swimmer  and  does  not  hesitate  to 
dive  and  swim  under  water  for  great  distances  when  alarmed.  It  makes 
nests  of  grasses  and  weeds  which  may  be  placed  under  a  mass  of 
tangled  debris  or  woven  into  the  rushes  a  foot  or  more  above  the  high 
water  level.  Its  presence  may  usually  be  detected  by  the  extensive  and 
well-defined  runways  it  makes  and  by  the  mats  of  cut  vegetation  float- 
ing at  irregular  intervals  in  the  tidal  waters.  Sometimes,  however, 
there  may  be  little  evidence  of  rice  rats  in  an  area.  Harris  (1953,  p. 
481)  says  that  in  the  Blackwater  National  Wildlife  Refuge  in  Dor- 
chester County  40  percent  of  the  86  rice  rat  captures  were  made  at 
trap  stations  showing  no  signs  of  small  mammals,  but  some  were  taken 
at  muskrat  houses.  Also,  he  was  never  able  to  locate  any  rice  rat  nests 
in  this  area,  and  noted  that  only  a  few  of  the  runways  found  light 
have  been  made  by  this  species.  Rice  rats  are  primarily  nocturnal,  and 
Harris  states  that  only  rarely  was  this  species  observed  in  the  dajlime. 

In  Maryland,  rice  rats  are  confined  in  distribution  to  the  fresh  and 
salt  water  marshes  of  the  Western  Shore  and  Eastern  Shore  sections. 
They  seem  to  be  particularly  numerous  in  the  fresh,  brackish,  and  salt 
water  marshes  of  the  lower  Eastern  Shore  section  and  occur  in  great 
numbers  on  Assateague  Island,  where  they  occupy  the  wetter  portions 
of  these  marshes. 


90  NORTH  AMERICAN  FAUNA  66 

Specimens  examined. — Anne  Arundel  County :  South  River,  at  U.S. 
Eoiite  50,  1.  Charles  County:  Nanjemoy  Creek,  5.  Prince  Georges 
County:  Oxon  Hill,  2  miles  NW,  2.  Worcester  County :  Ocean  City,  4 
and  5  miles  S  ( Assateague  Island) ,  2 ;  West  Ocean  City,  4. 

Other  records  and  reports. — Dorchester  County :  Blackwater  Na- 
tional Wildlife  Refuge  (Harris,  1953) . 

EASTERN  HARVEST  MOUSE 
Reithrodontomys  humulis  virginianus  A.  H.  Howell 

Reithrodontowys  hun^ulis  virginianus  A.  H.  Howell,  Jour.  Mammal., 
21  (3)  :  346, 13  August  1940. 

Type  locality. — Amelia,  Va. 

General  distribution. — Known  from  central  Virginia  north  to  Maryland.  Exact 
northern  limits  of  range  unknown. 

Distribution  in  Maryland. — Rare  in  Maryland;  probably  occurs 
only  in  the  Western  Shore  and  southern  Piedmont  sections. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  0/0,  3/3,  =  16;  upper 
incisors  with  conspicuous  grooves;  mouselike  in  form;  tail  about  half 
total  length;  coloration  grayish-brown  above  with  a  distinct  band  of 
blackish  along  the  median  line;  sides  of  head  and  body  paler,  more  or 
less  washed  with  light  pinkish  cinnamon,  this  color  forming  a  definite 
lateral  line  next  to  the  belly;  underparts  grayish  white;  tail  bicolored, 
fuscous  above,  grayish  white  below;  ears  fuscous,  feet  white. 

This  species  closely  resembles  the  house  mouse  {Mus  musoulus)  in 
general  appearance,  but  may  readily  be  distinguished  from  that  species 
by  the  deeply  grooved  upper  incisors.  In  the  eastern  United  States 
the  harvest  mouse  is  the  only  long-tailed  cricetine  rodent  with  grooved 
incisors. 

Measurements. — An  adult  female  from  Takoma  Park  (near  Riggs 
Mill),  Prince  Georges  County,  measures  as  follows:  Total  length  132; 
tail  59 ;  hind  foot  15.5 ;  ear  12 ;  greatest  length  of  skull  20.0 ;  zygomatic 
breadth  10.1 ;  least  interorbital  breadth  2.9;  upper  molar  toothrow  2.5. 

Howell  (1940,  p.  346)  gives  external  measurements  of  10  specimens 
from  the  type  locality  as  follows:  Total  length  117.2  (110-125) ;  tail 
vertebrae  51.8  (45-56)  ;  hind  foot  16.2.  The  greatest  length  of  skull 
of  these  10  specimens  is  18.7  (18.3-19.1).  It  can  be  seen  that  the  Mary- 
land specimen  is  considerably  larger  both  externally  and  in  the  great- 
est length  of  the  skull  than  topotypes  of  the  subspecies  from  Amelia, 
Va. 

Habitat  cond  habits. — Tlie  harvest  mouse  prefers  nonforested  land, 
particularly  cultivated  fields  where  grain  crops  are  growing.  It  seems 
to  be  equally  at  home  in  dry  fields  or  in  bogs,  provided  there  is  thick 
growth  of  tall  grasses  or  sedges. 


MAMMALS  OF  MARYLAND 


91 


Reithrodontomys  humulis  virginianus 
•  Specimen  examined 


Figure  33. — Distribution  of  Rcithrodontomys  humulis  virginianus. 


Little  is  known  of  the  habits  of  this  species.  It  lives  in  the  cover 
of  grass,  weeds,  and  grains  where  it  makes  little  runways  over  the 
surface  of  the  ground.  According  to  Lewis  (1940,  p.  426),  in  Amelia 
County,  Va.,  it  generally  makes  nests  of  fine  grass  blades  on  top  of  the 
ground  in  tall  grass  or  sedges.  These  nests  are  globular  and  average 
larger  than  a  croquet  ball. 

The  breeding  season  is  from  May  to  November ;  the  number  of  young 
from  one  to  five ;  the  gestation  period  is  about  23  days. 

The  food  of  the  eastern  harvest  mouse  consists  largely  of  seeds  and 
grains  with  considerable  green  vegetation  and  occasionally  fruit 
(Howell,  1914,  p.  11). 

According  to  Bailey  (1923,  p.  118),  many  skulls  of  harvest  mice 
were  found  in  owl  pellets  in  the  Smithsonian  tower  in  Washington, 
D.C.  The  owl,  or  owls,  however,  may  have  been  feeding  in  nearby 
Virginia  and  thus  the  skulls  may  not  represent  District  of  Colmnbia 
or  Maryland  records.  This  rodent  species  has  been  trapped  at  only  one 
locality  in  Maryland. 

S'peclm<ens  examined. — Prince  Georges  County :  Takoma  Park  (near 
Riggs  Mill),  1.  Howell  (1940,  p.  346),  reported  examining  two  speci- 
mens from  Riggs  Mill,  and  records  in  the  files  of  the  U.S.  Fish  and 
Wildlife  Service  indicate  that  Ray  Greenfield  actually  took  three  spe- 
cimens in  that  same  area  on  26  January  1934.  Only  one  si^ecimen  from 
that  locality,  however,  is  now  in  the  National  collections. 


92  NORTH  AMERICAN  FAUNA  66 

DEER  MOUSE 
Peromyscus  maniculatus  (Wagner) 

Hespercnnys  maimcvZatus  Wagner,  Arch.  Naturgesch.,  Jahrg.  11,  1 : 
148,  1845. 

This  is  a  wide- ranging  species  that  occurs  over  much  of  North  Amer- 
ica. Numerous  subspecies  have  been  described ;  of  these,  two  are  known 
to  occur  in  Maryland.  They  are : 

Peromyscus  maniculatus  hairdii  (Hoy  and  Kennicott) 

Mus  hairdii  Hoy  and  Kennicott,  in  Kennicott,  Agricultural  Report, 
U.S.  C!ommissioners  Patents,  1856,  p.  92,  1897. 

Type  locality. — Bloomin^on,  McLean  County,  111. 

General  distribution. — Prairie  region  of  the  upper  Mississippi  Valley,  from 
eastern  Kansas  and  Missouri ;  north  to  southwestern  Manitoba,  Canada  ;  east- 
ward through  southern  Minnesota,  Wisconsin,  and  Michigan  to  the  man-made 
prairie  of  central  New  York,  Pennsylvania,  Maryland,  and  northern  Virginia. 

Distribution  in  Maryland. — The  distribution  of  this  subspecies 
within  the  State  is  unknown.  It  has  been  taken  in  Maryland  only  at  the 
Patuxent  Research  Center,  Prince  Georges  County.  (See  fig.  34.) 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  0/0,  3/3,  =  16; 
coloration  of  upperparts  brownish  gray,  mixed  with  darker  hairs; 
underparts  white,  the  basal  gray  of  the  underfur  often  conspicuous; 
tail  short  and  distinctly  bicolored,  upperparts  brownish  black,  white 
beneath;  feet  white.  Immature  animals  are  more  grayish  dorsally. 

This  subspecies  is  readily  distinguished  from  Peromyscus  manicula- 
tus rmbiterrae  by  its  much  shorter  tail.  It  is  easily  confused  with 
Peromyscus  leucofus^  but  may  be  distinguished  by  several  characters 
which  are  discussed  under  that  species. 

Measurements. — External  measurements  of  two  adults  from  the 
Patuxent  Research  (Center,  Prince  Georges  County,  (a  wild-caught 
female  and  one  of  her  laboratory-raised  offspring)  are  as  follows: 
Total  length  152,  149;  tail  63,  59;  hind  foot  18,  19;  ear  13.5,  14.0. 
Cranial  measurements  of  three  adults  from  the  Patuxent  Research 
(3enter  (the  wild-caught  female  and  two  of  her  laboratory-raised  off- 
spring) are:  Greatest  length  23.1,  23.3,  23.0;  zygomatic  breadth  11.5, 
12.1,  11.9;  interorbital  breadth  3.7,  3.9,  3.9;  length  of  maxillary  tooth- 
row  3.0,  3.3,  3.3. 

Habitat  and  hahits. — This  subspecies  inhabits  prairies,  open  fields, 
and  arable  land  and  is  entirely  absent  from  dense  forests.  It  was  un- 
known in  Maryland  until  1949,  when  Lucille  F.  Stickel  and  Oscar 
Warbach  live-trapped  several  in  crop  fields  at  the  Patuxent  Research 
Center.  These  fields  are  about  1.9  miles  north  of  Bowie  and  are  situated 
on  a  wide  bench  of  sandy  clay  near  the  Patuxent  River.  From  May 


MAMMALS  OF  MARYLAND  93 

1949  to  June  1950,  23  of  these  mice  were  captured  by  Stickel  and 
Warbach. 

According  to  W.  H.  Stickel  (1951,  p.  26)  the  Maryland  specimens 
of  this  race  were  most  often  caught  in  corn  and  in  young  wheat ;  only 
occasionally  were  they  found  in  hay  or  tall  wheat.  He  says  that  the 
subspecies  seems  to  be  precariously  established  at  the  Patuxent  Re- 
search Center  and  was  not  common,  nor  did  the  numbers  appear  to 
increase,  during  the  year  the  area  was  extensively  studied. 

Peromyscus  m.  hairdii  is  essentially  a  subspecies  of  the  prairie  re- 
gion of  the  upper  Mississippi  Valley.  In  recent  years  it  appears  to  have 
been  extending  its  range  eastward  consequent  with  the  deforestation 
of  wide  areas  of  land  in  the  eastern  United  States,  In  1909,  Osgood 
(1909,  p.  79)  knew  it  only  from  as  far  east  as  Ohio.  In  1934,  Mitchell 
(1934,  p.  71)  recorded  it  from  Meadville,  Pa.,  and  in  1938,  Moulthrop 
(1938,  p.  503)  listed  it  from  Elba,  Genesee  County,  N.Y.  Hamilton 
( 1950,  p.  100)  recorded  the  first  appearance  of  hairdii  in  1947  at  Ithaca, 
N.Y.,  an  area  that  had  been  heavily  trapped  for  the  previous  20  years, 
and  mentioned  the  capture  of  the  subspecies  at  North  Harrisburg, 
Dauphin  County,  Pa,,  the  first  record  from  east  of  the  Appalachian 
Mountains.  More  recently.  Peacock  and  Peacock  (1962,  p,  98)  have 
taken  specimens  from  the  area  being  developed  into  Dulles  Airport, 
near  Chantilly,  Fairfax  County,  Va, 

Stickel  (1951,  p,  26)  states  that  no  doubt  the  animal  is  expanding 
its  range  by  natural  means  in  consequence  of  artificially  created  habi- 
tats, but  the  possibility  of  accidental  transportation  is  considerable. 
It  may  be  that  the  mouse  has  succeeded  in  crossing  the  heavily  forested 
Appalachian  Mountains  by  following  the  grass-lined  banks  and 
shoulders  that  line  the  roads  in  that  area.  It  would  in  this  way  remain 
ecologically  separated  from  P&roinyscus  m,  nubiterrae^  the  race  in- 
habiting the  dense  forests  of  the  Appalachians. 

Just  how  widely  hairdii  is  distributed  in  Maryland  is  unknown.  No 
additional  specimens  have  been  taken  since  Stickel  and  Warbach  col- 
lected those  at  the  Patuxent  Research  Center  in  1939.  I  have  trapped 
many  cultivated  fields  in  central  Maryland  and  grassy  roadsides  in 
the  western  part  of  the  State  with  the  hope  of  obtaining  additional 
records,  but  without  success.  The  recent  records  from  nearby  Chantilly, 
Va.,  however,  lead  me  to  believe  that  the  subspecies  is  probably  widely 
distributed,  although  perhaps  scarce  as  regards  total  numbers,  in  open 
fields  throughout  Maryland. 

These  mice  feed  largely  on  seeds,  grain,  and  the  ripe  heads  of  grasses ; 
berries  and  numerous  insects  are  also  consumed.  The  nest  is  built 
slightly  underground,  or  on  the  surface,  and  usually  placed  under 
some  object,  such  as  a  board,  fallen  tree  limb,  rock,  or  old  pasteboard 
carton.  The  breeding  season  generally  begins  in  early  March  and  ex- 

536-897  O — 69 7 


94 


NORTH  AMEBICANi  FAUNA  66 


tends  through  November.  A  female  may  breed  three  or  four  times 
yearly,  and  a  litter  may  contain  from  two  to  nine  young,  although  four 
to  six  is  the  most  common  number. 

Specimens  excmimed. — Prince  Georges  County:  Patuxent  Research 
Center,  3. 

Peromyscus  maniculatus  nubiterrae  Rhoads 

Peromyscus  leucopus  nuhiterrae  Rhoads,  Proc.  Acad.  Nat.  Sci.  Phila- 
delphia, 48 :  187,  April  1896. 

Type  locality. — Summit  of  Roan  Mountain,  Mitchell  Ck>unty,  North  Carolina. 
Altitude  6,370  feet. 

General  distribution. — Allegheny  and  Blue  Ridge  Mountains  and  adjacent 
ranges  from  western  Pennsylvania  and  New  York,  south  to  western  North  Caro- 
lina and  northeastern  Georgia. 

Distribution  in  Maryland. — Found  in  the  Allegheny  Mountain  sec- 
tion at  elevations  usually  above  2,500  feet. 

Distinguishing  characteristics. — Similar  in  coloration  and  size  to 
P.  m.  hairdii,  but  is  readily  distinguished  from  that  subspecies  by  its 
much  longer  tail,  which  is  more  than  half  the  total  length  of  the  ani- 
mal. Usually  nubiterrae  has  larger  ears  and  feet  than  bairdii. 

In  general,  nubiterrae  can  be  distinguished  from  Peromyscus  leuco- 
jms  by  certain  subtle  differences  in  coloration.  Some  specimens  of 
nubiterrae.,  however,  are  confusingly  similar  to  Peromyscus  leucopus^ 


Peromyscus  maniculatus  bairdii 
▲  Specimens  examined 

Peromyscus  maniculatus  nubiterrae 
•  Specimens  examined 
O  Specimens  reported 


FiQtJBE  34. — Distribution  of  Peromyscus  maniculatus  nubiterrae  and  P.  m.  bairdii. 


MAMMALS  OF  MARYLAND  95 

and  their  distinguishing  characteristics  are  discussed  in  more  detail 
under  that  species. 

Measurements. — Thirteen  adults  from  Finzel,  Garrett  County,  have 
external  measurements  as  follows:  Total  length  179.3  (172-190)  ;  tail 
93.1  (82-102) ;  hind  foot  20.5  (20-22).  Eleven  adults  from  Finzel  have 
the  following  cranial  measurements:  Greatest  length  24.6  (24.3-25.3) ; 
zygomatic  breadth  12.3  (11.7-13.3);  interorbital  breadth  3.7  (3.5- 
3.9) ;  maxillary  toothrow  3.3  (3.2-3.5). 

Habitat  and  habits. — This  subspecies  prefers  dense  woods  and  is 
most  abundant  among  mossy  boulders  and  logs  in  moist  spruce  and 
fir  forests  at  higher  elevations.  E.  A.  Preble  (in  field  notes)  gives 
information  about  where  he  took  specimens  in  Garrett  County.  He 
says  that  they  were  common  in  a  tract  of  hemlock  woods  about  3  miles 
east  of  Grantsville.  One  specimen  was  taken  in  a  small  strip  of  decidu- 
ous trees  and  shrubs  adjoining  a  field  where  Peromyscus  leuco'pus  was 
also  taken.  At  Finzel,  at  an  elevation  of  about  2,600  feet,  he  found  that 
these  mice  were  abundant  and  inhabiting  all  sorts  of  situations  from 
the  dry  hillsides  and  edges  of  fields  to  the  deep  hemlock  swamps,  while 
at  Bittinger  (elevation  about  2,600  feet)  they  were  abundant  only  in 
the  deep  woods. 

This  mouse  nests  in  burrows  under  rocks  aiid  logs  and  sometimes  in 
hollow  trees.  It  is  somewhat  arboreal  and  may  build  tree  nests  as  high 
as  50  feet  above  the  ground  (J.  W.  Bailey,  1946,  p.  216).  Two  or  three 
litters,  of  from  two  to  seven  young,  are  produced  each  season.  Food 
consists  of  seeds,  nuts,  and  berries,  supplemented  with  insects,  snails, 
and  occasionally  dead  birds  and  other  mice. 

Specimens  exan^in^d. — Allegany  County:  Frostburg,  1.  Garrett 
County:  Bittinger,  6 ;  Finzel,  18 ;  Grantsville,  16 ;  Swallow  Falls  State 
Forest  (near  Muddy  Creek  Falls) ,  1. 

Other  records  and  reports. — Garrett  County:  New  Germany  (Coll. 
Nat,  Hist.  Soc.  Maryland) . 

WHITE- FOOTED  MOUSE 

Peromyscus  leucopus  noveboracensis  (Fisher) 

[Mu^.  sylvaticus']  noveboracensis  Fisher,  Synopsis  Mammalium,  p. 
318,  1829. 

Type  locality. — New  York. 

General  distribution. — From  eastern  and  southern  Ontario,  east  to  Maine,  south 
along  the  Atlantic  coast  into  Virginia,  West  Virginia,  and  northern  Kentucky, 
westward,  south  of  Great  Lakes,  to  eastern  North  Dakota,  South  Dakota,  Ne- 
braska, northeastern  Oklahoma,  and  northwestern  Arkansas. 

Distribution  in  Marylamd. — Occurs  abundantly  in  all  sections  of  the 
State. 


96  NORTH  AMERICAN  FAUNA  66 


Peromyeaus   leucopus  noveboraaensis 
C  Specimens  examined 
O  Specimens  reported 


Figure  35. — Distribution  of  Peromyscus  leucopus  noveboracensis. 

Distinguishing  characteristics. — The  white- footed  mouse  closely  re- 
sembles the  deer  mouse  {Peromyscus  mamiculatus) ,  from  which  it  may 
be  distinguished  as  follows : 

From  Peromyscus  m.  hairdii  it  differs  in  being  larger,  longer  tailed, 
lighter  and  more  brightly  colored  with  more  reddish  on  sides  and  back, 
and  in  having  noticeably  larger  ears  and  feet ;  the  tail  is  less  distinctly 
bicolored. 

Cranially,  P.  7.  navehoraeensis  is  larger  than  P.  nh.  hairdii.,  and  the 
incisive  foramina  are  differently  shaped.  These  foramina  are  anteriorly 
constricted  in  noveboracensis,  and  open  and  evenly  curved  in  hairdii. 
A  detailed  comparison  of  these  two  forms  is  given  by  Stickel  (1951, 
p.  25-32). 

From  Peromyscus  m.  nuhiterrae,  P.  I.  novehoracensis  differs  in  being 
larger,  shorter  tailed,  (tail  less  than  half  the  total  length  of  the  animal) 
and  more  brightly  colored,  with  more  reddish  on  sides  and  back.  This 
color  difference  is  subtle  in  individual  specimens  but  becomes  apparent 
when  large  series  of  both  species  are  examined.  The  tail  in  novehora- 
censis is  less  distinctly  bicolored  than  in  nuhiterrae. 

Some  specimens  of  nuhiterrae  and  leucojms  are  so  similar  in  external 
characteristics  that  only  by  a  detailed  examination  of  the  skull  can  they 
be  separated.  The  skull  of  nuhiterrae  is  slender  and  elongated,  the 
braincase  considerably  flattened,  whereas  cranially  novehoracensis  is 
broader  and  heavier  with  the  braincase  more  inflated.  As  in  P.  m. 


MAMMALS  OF  MARYLANI>  97 

hairdii,  the  incisive  foramina  of  nubiterrae  are  open  and  evenly  curved, 
while  in  noveboracensis  they  are  anteriorly  constricted.  The  teeth  in 
the  latter  form,  even  in  juvenile  animals,  are  noticeably  larger  and 
more  robust  than  in  nubiterrae. 

Measurements. — External  measurements  of  eight  adults  from  Alle- 
gany County  (Dans  Mountain  State  Park,  and  vicinity  of  Oldtown) 
are  as  follows:  Total  length  174.4  (170-188) ;  tail  76.2  (70-92)  ;  hind 
foot  21.1  (20-22) ;  ear  15.7  (13-18).  Nine  adults  from  the  same  locali- 
ties have  the  following  cranial  measurements:  Greatest  length  26.2 
(26.0-26.7) ;  zygomatic  breadth  13.4  (12.7-14.0)  ;  interorbital  breadth 
4.1  (3.9-4.3) ;  maxillary  toothrow  3.6  (3.4-3.8). 

Habitat  and  habits. — This  species  is  primarily  a  woodland  inhab- 
itant, but  is  often  found  in  brushy  regions  and  sometimes  in  grassy 
areas  that  border  woodlands.  It  is  one  of  the  most  abundant  mammals 
in  Maryland.  On  Assateague  Island  their  tracks  have  been  observed 
even  on  the  bare  sand  dunes  a  few  yards  from  the  ocean  beach.  Usually, 
however,  this  mouse  will  be  found  not  more  than  50  feet  from  woods  or 
forests,  of  which  it  seems  to  prefer  the  deciduous  woods,  especially 
oak-hickory  forest. 

Nests  are  built  almost  anywhere.  Although  it  apparently  does  not 
dig  its  own  burrow,  or  make  a  trail,  this  mouse  will  utilize  burrows 
or  trails  of  other  small  mammals.  Jackson  (1961,  p.  218)  says  that  it 
seems  to  prefer  a  tree  site  for  its  nest,  usually  about  6  to  8  feet  from 
the  ground,  but  that  he  has  found  them  in  abandoned  squirrel  nests  as 
high  as  20  feet  above  ground.  He  says  that  often  the  nest  is  built  in 
a  hollow  tree  or  limb,  and  that  another  favorite  site  is  under  an  old 
stump  or  log.  The  nest  itself  is  composed  of  soft  material  such  as  grass, 
leaves,  or  other  vegetation.  It  is  usually  about  10  or  12  inches  in  diam- 
eter and  6  or  8  inches  deep. 

Breeding  takes  place  in  late  February  or  early  March,  and  the  first 
litter  is  bom  in  April.  The  gestation  period  is  variable,  but  is  usually 
between  23  and  25  days,  and  the  litter  size  varies  from  one  to  seven, 
usually  three  to  six,  with  four  the  most  frequent  number.  Each  female 
may  produce  as  many  as  four  litters  during  the  breeding  season. 

The  principal  food  for  the  species  is  seeds  of  various  grasses,  weeds, 
clover,  small  fruits,  and  grain  as  well  as  acorns  and  hickory  nuts.  In- 
sects form  a  small  portion  of  the  diet  as  does  green  herbage.  This  mouse 
sometimes  occupies  houses,  where  it  may  be  bothersome.  On  Assateague 
Island  in  1957  and  1958,  white-footed  mice  were  inhabiting  the  houses 
and  outbuildings,  while  house  mice  {Mu^  nuasculus)  occurred  in  the 
woods  and  marshes,  but  apparently  not  in  the  houses. 

Specimens  examiTied. — Allegany  County:  Dans  Mountain  State 
Park,  13;  Green  Ridge,  4;  Mount  Savage,  11;  Oldtown,  4  miles  E, 


98  NORTH  AMERIOANi  FAUNA  66 

31 ;  Oldtown,  9  miles  E,  12 ;  Rawlings,  2 ;  Sideling  Hill  Creek,  8.  Anne 
Arundel  County:  Annapolis,  3  miles  NW,  12;  Priest  Bridge,  4;  South 
River  (at  U.S.  Route  50),  10.  Baltimore  County:  Lake  Roland,  5; 
Loch  Raven,  7;  Notch  Cliff,  1.  Calvert  County:  Battle  Creek  (Cypress 
Swamp),  4;  Cove  Point,  3;  Drum  Point,  2;  Scientist  Cliffs,  1;  Solo- 
mons, 2;  Solomons,  31^  miles  N,  17.  Charles  County:  Nanjemoy  Creek, 
2;  Newport,  6;  Zekiah  Swamp,  4.  Dorchester  County:  Cambridge,  5. 
Garrett  County:  Cranberry  Swamp,  7;  Grantsville,  4;  Swallow  Falls, 
2  miles  S,  2;  S wanton,  3.  Howard  County:  Atholton,  6.  Montgomery 
County:  Burnt  Mills,  2;  Cabin  John  (vicinity  of),  4;  Cupids  Bower 
Island  (vicinity  of),  5;  Forest  Glen,  1;  Great  Falls,  1;  Kensington, 
5;  Linden,  2;  Plummers  Island,  4;  Rockville  (vicinity  of),  6;  Seneca 
Creek  (at  Clopper  Road),  5;  Silver  Spring,  26;  Takoma  Park,  1; 
Woodside,  1.  Prince  Georges  County :  Anacostia  River,  NW  Branch, 
3;  Bladensburg,  7;  Branchville,  2;  Broad  Creek  (Indian  Head  Bluff), 
4;  Collingwood  (=  Collington?)  1  mile  S,  2;  Hyattsville,  4 ;  Lanham, 
4;  Laurel,  10;  Oxon  Hill,  12;  Riggs  Mill,  1 ;  Riverdale,  3.  Washington 
County :  Bear  Creek,  just  N  of  U.S.  Route  40,  2.  Wicomieo  County: 
Powellsville,  1.  Worcester  County:  Snow  Hill,  1  mile  NE,  1;  Ocean 
City,  5  miles  S,  1.  District  of  Columbia:  62. 

Other  records  amd  reports. — Allegany  County:  La  Vale  (Coll.  U. 
Md.).  Anne  Arundel  County:  Dorsey  (U.S.  Fish  and  Wildlife  Serv- 
ice files).  Cecil  County:  Rising  Sun  (U.S.  Fish  and  Wildlife  Service 
files).  Garrett  County:  Muddy  Creek  Falls  (Mansueti  and  Flyger, 
1952,  p.  250).  Kent  Cmmty:  Chestertown  (U.S.  Fish  and  Wildlife 
Service  files).  Prince  Georges  County:  Bowie  (Lucille  F.  Stickel, 
1946,  p.  301). 

Remarks. — Specimens  from  the  Eastern  Shore  section  (Cambridge, 
Powellsville,  Snow  Hill,  and  Assateague  Island),  as  well  as  Virginia 
specimens  from  Accomack  and  Northampton  Counties  on  the  lower 
Delmarva  Peninsula,  are  not  typical  novehoracensis  but  are  somewhat 
darker  in  coloration,  and  smaller  in  size,  and  appear  to  be  intergrades 
with  P.  I.  leu/ioptis  (Rafinesque).  The  type  locality  of  P.  I.  leucofus 
is  in  western  Kentucky,  which  is  also  an  area  of  intergradation.  Mary- 
land specimens  from  the  Eastern  Shore  section  are  only  slightly  larger 
and  paler  than  specimens  from  western  Kentucky  near  the  type  lo- 
cality of  P.  I.  leucopus.  Nevertheless,  they  are  considerably  different 
from  P.  I.  leucopus  from  southern  Louisiana  (where  the  subspecies  is 
best  characterized)  both  in  size  and  coloration,  and  are  more  closely 
related  to  P.  I,  novehoracensis  from  central  New  England  where  nove- 
horacensis is  best  characterized)  than  to  Louisianan  P.  I.  leucopus. 


MAMMALS  OF  MARYLAND  99 

EASTERN  WOOD  RAT 

Neotoma  floridana  magister  Baird 

N[eotoma].  magister  Baird,  Mammals,  in  Kepts.  Expl.  Surv.  .  .  , 
8  (1):498,  14  July  1858. 

Type  locality. — Cave  near  Carlisle,  Cumberland  County,  or  near  Harrisburg, 
Dauphin  County,  Pa. 

General  distribution. — Appalachian  Mountain  region,  from  extreme  western 
Connecticut  and  southern  New  York,  south  through  western  Virginia  and  Ten- 
nessee to  the  Tennessee  River  in  northern  Alabama,  west  to  central  Kentucky 
and  northward  to  extreme  southern  Indiana. 

Distribution  m  Maryland. — The  Allegheny  Mountain  and  Ridge 
and  Valley  sections;  occurs  east  of  the  Blue  Ridge  Mountains  in  the 
Piedmont  section  along  the  cliffs  and  bluffs  of  the  Potomac  River  to 
the  vicinity  of  Washington,  D.C.  It  may  occur  among  the  cliffs  and 
bluffs  of  river  valleys  elsewhere  in  the  Piedmont  section. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  0/0,  3/3,  =  16; 
size  large;  coloration  grizzled  grayish  dorsaUy,  with  some  buffy 
intermixture,  paler  and  more  buffy  on  sides;  underparts  and  feet 
white;  ears  large  and  naked;  tail  long,  hairy,  and  distinctly  bicolored, 
black  dorsally  and  white  underneath;  vibrissae  very  long,  and  black 
or  white  in  coloration.  The  young  are  similar  to  the  adults,  but  are 
grayer. 

This  species  may  be  confused  with  the  Norway  rat,  which  it  resem- 
bles superficially.  It  may  be  distinguished  from  that  species  by  its 
larger  naked  ears,  its  much  longer  vibrissae,  its  longer,  more  hairy, 
and  bicolored  tail,  and  its  softer,  more  grizzled  grayish  coloration.  In 
addition,  the  molar  teeth  of  the  two  species  differ.  In  the  eastern  wood 
rat  the  crowns  are  flat,  with  the  enamel  thrown  into  prismatic  folds ; 
in  the  Norway  rat  the  molars  are  tuberculate. 

Measurements. — An  adult  male  from  9  miles  E  of  Oldtown,  Al- 
legany County,  measures  as  follows :  Total  length  430 ;  tail  188 ;  hind 
foot  42;  ear  30;  greatest  length  of  skull  56.2;  interorbital  breadth 
6.8 ;  length  of  nasals  21.5 ;  length  of  molar  toothrow  9.3. 

Hamilton  (1943,  p.  306)  gives  the  following  external  measurements 
for  10  adults  from  New  York,  Pennsylvania,  and  West  Virginia :  Total 
length  423  (405-441)  ;  tail  186  (170-200)  ;  hind  foot  43.5  (40-46). 

Habitat  and  habits. — The  eastern  wood  rat  prefers  cliffs,  rock  slides, 
caves,  and  bare  patches  in  the  moimtainous  regions  of  the  State.  It 
ranges  into  the  Piedmont  section  at  least  in  the  Potomac  River  Valley, 
where  it  lives  in  the  cliffs  and  rocks  that  border  the  river.  It  may  occur 
in  the  bluffs  that  border  other  rivers  in  the  Piedmont  section,  and  has 
been  reported  from  Woodside,  Montgomery  County  (Wetmore,  1923, 
p.  187).  In  the  Potomac  River  Valley,  it  has  been  found  as  far  south 


100  NORTH  AMEBICANi  FAUNA  66 


Neotoma  flondana  magieter 
9  Specimens  examined 
O  Specimens  reported 


Figure  36. — Distribution  of  Neotoma  floridana  magister. 

as  Plummers  Island,  Montgomery  County,  and  on  the  Virginia  side  of 
the  river  at  Chain  Bridge. 

Wood  rats  were  particularly  abundant  in  the  vicinity  of  Oldtown, 
Allegany  County,  in  the  fall  of  1961,  where  virtually  every  rocky  out- 
cropping contained  signs  of  them,  Tliey  had  taken  up  residence  under 
the  front  porch  of  a  hunting  cabin  9  miles  east  of  Oldtown,  and  the 
sounds  of  their  activity  could  be  heard  all  night.  They  are  inquisitive 
animals,  and  one  had  thoroughly  explored  an  automobile  that  was 
parked  nearby,  even  crawling  into  the  engine  compartment,  leaving 
tracks  everywhere  in  the  dust. 

The  eastern  wood  rat  appears  to  have  moved  into  Maryland's  Pied- 
mont section  only  within  recent  years,  Wetmore  (1923,  p,  187)  reports 
that  although  Plummers  Island  had  been  under  observation  by  Wash- 
ington naturalists  since  1902,  it  wasn't  until  1921  that  the  species  was 
discovered  to  be  resident  there.  It  was  known,  however,  to  inhabit  the 
cliffs  along  the  Virginia  side  of  the  Potomac  River  as  far  south  as 
Chain  Bridge  for  many  years  before  it  was  first  reported  from  Plum- 
mers Island,  and  it  seems  probable  that  the  Plummers  Island  popula- 
tion crossed  over  from  Virginia  during  a  winter  when  the  Potomac 
was  frozen  over,  Wetmore  (1923)  says  that  one  was  killed  on  Plum- 
mers Island  on  25  June  1921,  by  Mr,  W,  R.  Maxon,  but  was  not  pre- 
served. On  26  September  and  15  October  1921,  two  specimens  were 
collected  and  preserved  in  the  Biological  Survey  collection.  In  the 


MAMMALS  OF  MARYLAND  101 

same  year,  five  nests  of  this  species  were  discovered  beneath  the  cabin 
on  the  island. 

Wetmore  (1923)  describes  the  nests  of  the  eastern  wood  rat  on 
Plummers  Island  as  being  composed  of  bits  of  finely  shredded  cedar 
bark  and  similar  materials  that  formed  a  flattened  mass  12  to  15  inches 
across  with  a  small  depression  in  the  center.  As  it  was  warm  weather 
the  cavities  were  open  above,  but  the  walls  were  so  arranged  that  they 
could  be  pulled  out  to  form  a  domed  covering  if  the  need  for  greater 
warmth  arose. 

Wood  rats  eat  practically  any  vegetation  they  can  obtain,  including 
fruits  and  berries,  fungi,  ferns,  rhododendron,  and  a  host  of  others. 
The  species  breeds  from  spring  until  fall,  and  as  many  as  three  broods 
may  be  raised  annually.  The  gestation  period  is  30  to  36  days,  and  one 
to  three  young  are  usually  born. 

Specimens  examined. — Allegany  County:  Mount  Savage,  1  (Coll. 
U.  Md.)  ;  Oldtown,  9  miles  E,  1.  Garrett  County :  Backbone  Mountain, 
Savage  River  Dam  Site,  2  (Coll.  U.  MA.).  Montgomery  County:  Plum- 
mers Island,  2,  Washington  Coum,ty:  Bear  Creek,  just  north  of  U.S. 
40,1  (Coll.U.Md.). 

Other  records  and  reports. — Montgomery  County:  Perry's  Island 
(Wetmore,  1923 :  187) ;  Woodside  (Wetmore,  1923 :  187). 

RED-BACKED  MOUSE 
Clethrionomys  gapperi  gapperi  (Vigors) 

Arvicola  gapperi  Vigors,  Zool.  Jour.,  5 :  204,  1830. 

Type  locality. — Between  York  [Toronto]  and  Lake  Simeoe,  Ontario,  Canada. 

General  distrihuUon. — Massachusetts  south  in  the  Appalachians  to  western 
Virginia  and  west  through  New  York,  northern  Michigan,  and  southern  Ontario 
to  eastern  Minnesota. 

Distribution  vn  Marylamd. — Occurs  on  the  cooler  forested  slopes  in 
the  Ridge  and  Valley  and  Allegheny  Mountain  sections. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  0/0,  3/3,  =  16; 
cheek  teeth  rooted  in  adults;  size  medium;  coloration  of  upper  parts 
rusty  red,  becoming  buffy  on  the  sides  and  around  the  face;  under- 
parts  buffy  white;  tail  less  than  a  third  of  total  length  of  animal,  and 
bicolored,  blackish  above,   paler  below. 

This  mouse  may  be  distinguished  from  most  other  Maryland  mice 
by  its  reddish  coloration  and  short  tail.  It  resembles  the  pine  mouse, 
however,  in  both  these  characters,  but  differs  in  that  the  reddish 
coloration  is  confined  to  the  dorsum,  whereas  in  the  pine  mouse  the 
reddish  coloration  extends  onto  the  sides.  In  addition,  the  ears  of  the 
red-backed  mouse  are  larger,  the  tail  is  considerably  longer,  and  the 
fur  is  longer,  coarser,  and  less  mole-like. 


102 


NORTH  AMERICAN  FAUNA  66 


Clethrionomys  gapperi  gappen 
0    Specimens  examined 


Figure  37. — Distribution  of  Clethrionomys  gapperi  gapperi. 

Measurements. — Ten  adults  from  Garrett  County  have  the  follow- 
ing external  and  cranial  measurements :  Total  length  147.3  (140-155)  ; 
tail  42.9  (38-48)  ;  hind  foot  19.5  (19-20) ;  condylobasal  length  of  skull 
24.9  (24.1-25.8)  ;  zygomatic  breadth  13.3  (13.0-13.7) ;  interorbital 
breadth  4.0  (3.9-4.2) ;  length  of  molar  toothrow  54  (5.2-5.6). 

Habitat  and  habits. — ^This  mouse  prefers  cool,  damp,  forested  areas 
where  it  lives  among  the  mossy  rocks  and  rotten  logs.  In  the  northern 
part  of  its  range  it  is  widely  distributed,  but  in  Maryland  it  is  re- 
stricted to  the  higher  mountains,  where  it  is  locally  abundant.  Preble 
(field  notes)  took  the  red-backed  mouse  at  Finzel  on  the  border  of  a 
hemlock  woods,  and  at  Grantsville  he  found  that  it  was  very  common 
in  a  tract  of  hemlocks  3  miles  east  of  the  town.  It  was  also  abundant 
in  the  mixed  forest  covering  the  steep  slopes  on  the  east  side  of  the 
Castleman  River,  and  in  the  hemlock  woods  near  Bittinger.  At  Moun- 
tain Lake  Park,  Preble  took  a  specimen  among  rocks  in  an  oak  woods, 
and  at  Swanton  he  trapped  a  very  dark  individual  in  deep  hemlock 
woods.  Bookhout  tells  me  that  he  trapped  one  in  Allegany  County  in 
a  rock  outcrop  in  a  second-growth  oak-hickory  forest. 

This  species  does  not  make  elaborate  tunnels,  but  will  occupy  those 
made  by  moles  and  shrews.  Jackson  (1961,  pp.  227-228)  has  described 
a  nest  in  detail.  It  was  located  among  the  rootlets  of  small  trees  and 
was  some  3  inches  in  diameter.  The  nest  was  merely  a  small  carpet  of 
grass  stems  and  a  few  particles  of  dead  leaves  and  moss,  the  entire 


MAMMALS  OF  MARYLAND  103 

bulk  of  which  would  be  no  larger  than  a  man's  thumb.  Another  nest 
was  located  at  a  depth  of  about  18  inches  under  a  rotten  elm  stump.  It 
was  situated  on  top  of  the  soil  underneath  a  root  of  the  stump,  and 
was  4  inches  in  diameter  and  about  1  inch  in  depth,  slightly  hollow 
and  without  cover  other  than  the  log  abovB.  It  was  composed  of  small 
pieces  of  dry  leaves,  bark,  hazelnut  shells,  hemlock  cones,  twigs,  dry 
sphagnum,  and  green  moss. 

According  to  Hamilton  (1941,  p.  259),  in  New  York  State  about 
three- fourths  of  the  food  of  this  species  is  composed  of  green  vegeta- 
tion. In  addition,  a  large  part  of  the  diet  consists  of  nuts  and  seeds. 
Insects  are  not  as  often  eaten  as  they  are  by  white-footed  mice. 

The  red-backed  mouse  does  not  hibernate,  but  it  does  actively  gather 
stores  in  the  fall  in  preparation  for  winter.  The  breeding  season  is 
protracted,  beginning  in  the  late  winter  or  early  spring  and  extending 
well  into  fall.  One  litter  follows  another  during  the  breeding  season, 
and  from  two  to  eight  young  comprise  a  litter.  The  gestation  period 
is  17  to  19  days. 

Specimens  examined. — Allegany  County:  Mount  Savage,  6  (Coll. 
IT.  Md.) ;  Town  Hill  Mountain,  near  beacon  light,  1  (Coll.  U.  Md.). 
Garrett  County:  Bittinger,  7;  Cranberry  Swamp,  4  (Coll.  U.  Md.) ; 
Finzel,  5 ;  Grantsville,  3  miles  E,  15 ;  Mountain  Lake  Park,  1 ;  Swallow 
Falls  State  Forest  (near  Muddy  Creek  Falls) ,  1 ;  Swanton,  1 ;  Thayer- 
ville  Swamp,  2  (Coll.  U.  Md.)  ;  Wolf  Swamp,  1. 

Remarks. — Maryland  C.  g.  gapperi  average  somewhat  darker  and 
slightly  larger  than  specimens  of  this  subspecies  from  Ontario  and 
central  New  York.  They  appear  to  be  intergrades  between  C.  g.  gapperi 
and  C.  g.  caroUnensis  but  are  more  closely  related  to  the  former.  The 
specimen  collected  by  Preble  in  the  deep  hemlock  woods  at  Swanton 
is  as  dark  and  large,  however,  as  typical  caroUnensis. 

MEADOW  VOLE 
Microtus  pennsylvanicus  (Ord) 

Two  races  of  this  widespread  and  abundant  small  mammal  are 
recognizable  in  Maryland.  They  are : 

Microtus  pennsylvanicus  pennsylvanicus  (Ord) 

Mits  pennsylvanicus  Ord,  in   Guthrie,  a  new  geogr.,  hist.,  comm. 
grammar  .  .  .  Philadelphia,  2d  Amer.  ed.,  2:  292,  1815. 

Type  locality. — Meadows  below  Philadelphia,  Pa. 

General  distribution. — From  Quebec  and  New  Brunswick,  south  into  Georgia, 
and  west  into  Nebraska,  South  Dakota,  and  North  Dakota. 

Distribution  in  Maryland. — Distributed  in  the  Piedmont,  Ridge  and 
Valley,  and  Allegheny  Mountain  sections.  Intergrades  with  Microtus 


104  NORTH  AMERICANi  FAUNA  66 

/>.  nigrans  in  the  Eastern  Shore  and  Western  Shore  sections,  and  is  re- 
placed by  that  subspecies  in  the  southern  Eastern  Shore  and  southeast- 
ern Western  Shore  sections.  (See  fig.  38.) 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  0/0,  3/3,  =  16; 
molar  teeth  rootless  and  persistently  growing;  coloration  of  upper- 
parts  dull  chestnut  brown,  darkest  along  the  middle  of  the  back; 
underparts  grayish  white,  or  buffy  white;  feet  grayish  brown;  tail 
dusky  above,  paler  below,  fur  overlaid  with  coarse  guard  hairs; 
tail  less  than  a  third  of  total  length  of  animal. 

This  vole  is  similar  in  appearance  to  the  red-backed  mouse 
( Clethrionomys  gappeH) ,  but  is  larger  and  more  brownish  in  colora- 
tion, and  lacks  the  red  dorsal  band.  It  is  also  similar  in  appearance  to 
the  pine  vole  {Pitymys  pinetorum)  but  has  coarser  pelage,  bigger  ears, 
and  a  longer  tail.  It  dilEfers  from  the  southern  bog  lemming  {Synap- 
tomys  cooperi)  in  its  coarser,  shorter  pelage  and  much  longer  tail, 
and  in  lacking  grooved  upper  incisors. 

Measurements. — Eleven  adults  from  the  vicinity  of  Oldtown, 
Allegany  County,  have  the  following  external  and  cranial  measure- 
ments: Total  length  169.2  (161.0-187.0) ;  condylobasal  length  of  skull 
28.5  (28.1-29.0);  zygomatic  breadth  15.4  (14.8-15.9);  interorbital 
breadth  3.6  (3.4-4.0) ;  maxillary  toothrow  6.9  (6.5-7.3).  Males  average 
somewhat  larger  than  females. 

Habitat  and  habits. — This  vole  is  numerous  in  fields  and  meadows 
throughout  the  State.  It  is  also  common  in  marshes  and  similar  areas 
with  heavy  growth  of  grass ;  occasionally  it  is  found  in  orchards  and 
open  woodland  if  the  ground  cover  is  grassy.  This  is  one  of  the  most 
abundant  mammals  in  Maryland. 

Meadow  voles  construct  extensive  runways  on  the  surface  of  the 
ground.  These  runways  are  about  IY2  inches  in  diameter  and  run  in 
a  network  under  the  cover  of  dead  grass.  They  are  sometimes  the 
only  sign  of  the  presence  of  these  voles  in  an  area.  If  the  runway  is 
fresh  and  is  being  used,  there  will  generally  be  droppings  and  cut 
pieces  of  grass  at  various  intervals  along  it.  The  nest  of  the  meadow 
vole  is  usually  constructed  on  the  surface  of  the  ground  in  one  of  the 
runways.  It  is  bulky,  generally  about  5  or  6  inches  in  diameter  and 
3  or  4  inches  deep,  usually  covered,  but  sometimes  not. 

The  meadow  vole  is  active  both  day  and  night.  It  is  cyclic  in  nature 
and  the  reproductive  habits  vary  from  year  to  year  (Hamilton,  1937). 
It  is  polyestrous  and  may  breed  the  year  round,  although  in  Mary- 
land there  is  a  tendency  not  to  breed  during  the  coldest  part  of  win- 
ter. The  females  reach  puberty  and  begin  to  breed  at  25  days  of  age, 
and  from  six  to  eight  young  generally  comprise  a  litter.  The  gestation 
period  in  this  species  is  21  days,  or  a  little  less,  and  as  many  as  17 
litters  may  be  produced  in  a  year. 


MAMMALS  OF  MARYLAND  105 

The  food  of  the  meadow  vole  consists  chiefly  of  fresh  grass,  sedges, 
grains,  and  seeds.  Green  vegetation  comprises  the  major  portion  of 
its  diet  in  the  spring  and  summer,  while  in  the  fall,  grains  and  seeds 
are  an  important  commodity.  In  winter,  bark  and  roots  of  shrubs 
and  trees  are  sometimes  consumed. 

Hamilton  (1943,  p.  327)  says  that  the  meadow  vole  is  of  great  eco- 
nomic importance.  By  girdling  fruit  trees  and  nursery  stock  it  causes 
monetary  loss  to  the  horticulturist.  The  amount  of  forage  crops  it 
consumes,  while  difficult  to  measure,  is  in  the  aggregate  a  very  great 
loss  to  the  farmer.  It  does,  however,  perform  a  useful  function  in 
providing  predatory  birds  and  mammals  with  an  abundant  source  of 
food. 

Specimens  examined. — Allegany  County:  Cumberland,  2;  Mount 
Savage,  8;  Oldtown,  4  miles  E,  19;  Oldtown,  9  miles  E,  74;  Sideling 
Hill  Creek,  3.  Anne  Arundel  County:  Annapolis,  1  mile  W,  6;  Annap- 
olis, 3  miles  W,  4;  Annapolis,  4  miles  W,  2;  Lake  Shore  area,  1. 
Baltimore  County :  Loch  Raven,  2.  Charles  County :  Nanjemoy  Creek, 
2;  Newport,  5.  Garrett  County:  Finzel,  1;  Grantsville,  1;  Mountain 
Lake  Park,  2.  Hoioard  County :  Atholton,  i/^  mile  S,  5;  Long  Corner, 
1.  Montgomery  County:  Cabin  John  Bridge,  1  mile  N,  1 ;  Kensington, 
1 ;  Rockville,  2.3  miles  NE,  3 ;  Seneca,  li/g  miles  NW,  26 ;  Seneca,  2.9 
miles  W,  52;  Silver  Spring  (vicinity),  5.  Prince  Georges  County:  Col- 
lingwood  (=Collington?),  i/^  mile  S,  2;  Hyattsville,  10;  Lanham,  1; 
Laurel,  30;  Oxon  Hill,  11;  Riggs  Mill,  1.  Queen  Annes  County: 
Parson  Island,  2.  District  of  Columbia:  91. 

Other  records  and  reports. — Allegany  County:  Dans  Mountain 
(Coll.  U.  Md.) ;  La  Vale  (Coll.  U.  Md.) ;  McCoole  (Coll.  Carnegie 
Museum).  Anne  Anmdel  County:  Dorsey  (U.S.  Fish  and  Wildlife 
Service  files).  Baltimore  County:  Bare  Hills-Lake  Roland  area 
(Bures,  1948,  p.  67) ;  Patapsco  State  Park  (Hampe,  1939,  p.  6).  Gar- 
ret County:  Cranberry  Swamp  (Coll.  U.  Md.).  Cranes ville  Pine 
Sw^amp  (Mansueti,  1958,  p.  83)  ;  Cunningham  Swamp  (Coll.  U.  Md.). 
Prince  Georges  County:  Patuxent  Research  Center  (Herman  and 
Warbach,1956,p.87). 

Remarks. — This  subspecies  intergrades  with  Microtus  p.  nigrans  in 
the  Eastern  Shore  and  Western  Shore  sections.  Specimens  from  the 
northern  portion  of  these  sections  (Parson  Island,  Annapolis  vicinity. 
Laurel,  Oxon  Hill)  are,  however,  clearly  referable  to  M.  p.  pennsyl- 
vanicus,  as  is  a  small  series  from  New^port,  in  the  south  central 
Western  Shore  section. 


106 


NORTH  AMERICANi  FAUNA  66 


Microtus  pennsylvanicus  nigrans  Rhoads 

Microtus   pennsylvanicus   nigrans   Rhoads,    Proc.    Acad.    Nat.    Sci. 

Phila.,  49 :  307, 18  June  1897. 

Type  locality. — Currituck,  Currituck  County,  N.C. 

General  distribution. — Near  the  coast  from  southeastern  Maryland  to  north- 
eastern North  Carolina. 

Distribution  in  Maryland. — Southern  Eastern  Shore  section  at  least 
as  far  north  as  Cambridge,  Dorchester  County,  and  southeastern 
Western  Shore  section  in  Calvert  and  probably  St.  Marys  Counties. 
This  subspecies  intergrades  with  Microtus  p.  pennsyVvanicus  in  the 
central  portion  of  the  Western  Shore  section  and  in  the  northern  part 
of  the  Eastern  Shore  section. 

Distinguishing  characteristics. — Similar  to  Microtus  p.  pennsylva- 
nicus except  that  it  is  somewhat  larger  and  has  a  darker  coloration, 
almost  black  in  some  pelages. 


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f                      f 

1 

V 

76« 

aaa 

Figure  38. — Distribution  of  Microtus  pennsylvanicus  pennsylvanicus  and  M.  p. 

nigrans. 


Measurements. — External  and  cranial  measurements  of  seven  adults 
from  Drum  Point,  Calvert  County,  are  as  follows:  Total  length  173.1 
(168-184) ;  tail  47.8  (42-52) ;  hind  foot  22.6  (22-23) ;  ear  14.3  (12- 
16) ;  condylobasal  length  of  skull  29.1  (28.1-30.5) ;  zygomatic  breadth 


MAMMALS  OF  MARTLANB  107 

15.9  (15.4^16.6) ;  interorbital  breadth  3.8  (3.5^.0) ;  maxillary  tooth- 
row  6.8  (6.6-6.9). 

Habitat  and  habits. — In  the  southern  Eastern  Shore  section,  this 
subspecies  abounds  in  the  dryer  portions  of  brackish  and  salt  marshes 
along  the  Atlantic  seacoast  and  the  Chesapeake  Bay.  It  is  probably 
the  most  abundant  mammal  occurring  on  Assateague  Island.  As  an  ex- 
ample of  its  numbers  on  this  outer  barrier  island,  it  may  be  noted 
that  in  a  single  night  in  the  spring  of  1956,  60  specimens  were  taken 
in  100  traps  set  in  tall  grass  and  myrtle  on  the  edge  of  a  fresh  water 
impoundment  on  the  Virginia  portion  of  the  island  a  few  miles  south 
of  the  Maryland  line.  It  also  lives  in  the  marshes  of  the  Blackwater 
National  Wildlife  Kefuge  in  Dorchester  County  where  it  builds  nests 
in muskrat houses  (Harris,  1953) . 

In  the  Western  Shore  section,  in  Calvert  County,  this  vole  has 
been  taken  in  dry  meadows  and  brushy  fields. 

The  habits  of  this  subspecies  apparently  differ  in  no  essential  respect 
from  those  of  Miorotus  p.  pennsylvanicus. 

Specimens  exwrmrved. — Calvert  County:  Breezy  Point,  1;  Drum 
Point,  12;  Scientists  Cliffs  Road  (1  mile  E  Route  2),  2.  Dorchester 
Govmty:  Blackwater  National  Wildlife  Refuge,  5 ;  Cambridge,  5.  Wor- 
cester C&wnty:  Assateague  Island,  4  and  5  miles  S  Ocean  City,  10. 

PINE  VOLE 

Pitytnys  pinetorum  scalopsoides  (Aud.  and  Bachman) 

Arvicola  scalopsoides  Audubon  and  Bachman,  Proc.  Acad.  Nat.  Sci. 
Philadelphia,  1 :  97,  October  1841. 

Type  locality. — Long  Island,  N.Y, 

General  distribution. — Northeastern  United  States,  from  central  New  England, 
south  to  Virginia  and  western  North  Carolina,  west  to  Illinois  and  Wisconsin. 

Distribution  in  Maryland. — Common  in  all  sections  of  the  State. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  0/0,  3/3,  =  16; 
molar  teeth  not  rooted,  and  grow  persistently;  tail  very  short,  buffy 
brown  above,  lighter  below;  ears  very  short,  and  hidden  in  fur; 
pelage  short,  soft  and  glossy,  almost  mole-like;  coloration  russet  to 
chestnut  brown  on  dorsum,  becoming  lighter  on  sides;  underparts 
grayish  buff;  feet  grayish  brown. 

This  species  resembles  the  meadow  vole  [Miorotus  pennsylvanicus) 
from  which  it  may  be  distingiiished  by  its  shorter  tail,  shorter  ears, 
and  finer,  more  russet  pelage.  It  differs  from  the  red-backed  mouse 
{Clethrionomys  gapperi)  in  that  the  reddish  coloration  of  the  dorsum 
extends  onto  the  sides  and  is  not  confined  to  a  band  on  the  dorsum ; 
smaller  ears;  shorter  tail;  fur  shorter,  softer  and  more  mole-like. 


108 


NORTH  AMERICANi  FAUNA  66 


79-                                                           76" 
1                                                                  ' 

V 

^r 

rj, 

i 

p«r^ 

■ 

8 

1 

-39«- 

SCALE 
O        lO      20      30MILES 

m 

1 

-ss»- 

Pitymye  pinetorum  scalopsoides 
•    Specimens   examined 

^lITIIftl  IWi 

O    Specimens   reported 

^"'^'^^M/l/n 

^'^ 

'^nillM 

nJ-liii  ul 

-36'- 

"^ 

% 

m 

#■ 

rj.                                     r*^' 

1 

1 

76» 

....        ,       .    .9P« 

Figure  39. — Distribution  of  Pitymys  pinetorum  scalopsoides. 

From  the  southern  bog  lemming  {Synaptomys  cooperi)  this  species 
may  be  readily  distinguished  by  the  lack  of  grooves  on  the  upper 
incisors. 

Measv^ements. — Ten  adults  from  the  District  of  Columbia  have 
the  following  external  measurements:  Total  length  124.8  (120-131) ; 
tail  22.1  (15-25);  hind  foot  16.6  (16-18).  Eleven  adults  from  the 
District  of  Columbia  have  cranial  measurements  as  follows:  Con- 
dylobasal  length  24.9  (24.2-25.9)  ;  zygomatic  breadth  15.5  (14.2-16.3) ; 
interorbital  breadth  4.2  (3.9-4.6) ;  length  of  maxillary  toothrow  6.1 
(5.8-6.5). 

Habitat  and  habits. — This  species  is  not  particular  with  regard  to 
habitat  preference,  being  found  in  old  fields,  wood  borders,  and  culti- 
vated fields,  especially  in  loose  sandy  soils.  It  is  often  found  in  old 
apple  orchards  where  the  soil  is  mellow  and  sandy,  and  the  grass 
and  weeds  have  been  allowed  to  grow,  forming  a  heavy  protective 
carpet  of  vegetation.  The  fallen  apples  also  provide  the  mice  with 
food  in  autumn,  and  the  bark  of  apple  roots  supply  a  favorite  winter 
food.  Contrary  to  its  name,  the  pine  vole  is  seldom  found  in  pine  woods 
in  Maryland. 

Hamilton  (1938,  pp.  163-170)  in  his  life  history  study  of  the  spe- 
cies says  that  the  animal  threads  its  way  just  beneath  the  thick  carpet 
of  leaves  which  forms  a  ceiling  to  its  burrow.  Rarely  the  pine  vole 
tunnels  to  a  depth  of  a  foot  or  more,  but  by  far  the  greater  number 


MAMMALS  OF  MARYLAND  109 

of  burrows  are  shallow,  descending  to  a  depth  of  only  3  or  4  inches. 
In  orchards  it  tunnels  its  way  to  fallen  apples,  and  then  burrows  up 
from  underneath  to  feed  on  the  fruit.  These  mice  seldom  leave  their 
subterranean  burrows. 

The  nest  of  the  pine  vole  is  globular  in  shape,  and  composed  of 
almost  any  material  the  animal  can  procure,  generally  dead  leaves 
and  grasses.  The  nest  may  be  just  below  the  ground  surface,  or,  oc- 
casionally under  some  shallow-rooted  stump.  Usually  there  are  three 
or  four  exits. 

This  species  feeds  largely  on  roots  and  tubers,  bulbs,  and  the  bark 
of  trees  and  shrubs.  It  seldom  eats  green  vegetation,  seeds,  or  most 
kinds  of  fruit,  although  it  does  relish  apples  and  pears.  Generally, 
considerable  quantities  of  roots  and  tubers,  which  presumably  are 
utilized  as  the  bulk  of  the  winter  food,  are  stored  in  its  burrows.  Pine 
voles  often  are  responsible  for  depredations  in  orchards,  where  they 
frequently  girdle  apple  trees  severely. 

This  species  is  cyclic,  and  according  to  Hamilton  (1938,  p.  166)  its 
reproductive  behavior  undoubtedly  varies  from  year  to  year  as  does 
that  of  Microtus.  The  breeding  season  is  from  early  March  to  mid- 
November,  and  small  litters  of  from  two  to  four  young  are  produced. 
Tlie  gestation  period  in  all  probability  approximates  the  21  days  of 
Microtus. 

SpeciTTvens  examined. — Allegany  County:  Oldtown,  9  miles  E,  4. 
Awne  Anmdel  County:  Annapolis,  3  miles  NW,  2;  Lake  Shore  area, 
2.  Calvert  County :  Plum  Point,  2  miles  W,  1 ;  Solomons  Island,  3i/^ 
miles  N,  1.  Carroll  County:  Hampstead,  1.  Charles  County:  Newport, 
3;  Port  Tobacco,  3  miles  SW,  1.  Dorchester  County:  Cambridge,  3. 
Garrett  County:  Grantsville,  1.  Howard  County:  Long  Comer,  1. 
Montgomery  County:  Chevy  Chase,  1;  Kensington,  2;  Montg-omery 
Knolls,  1 ;  Plummers  Island,  5 ;  Poolesville,  1  mile  NE,  1 ;  Eockville, 
2.3  miles  NE,  10;  Seneca,  1.3  miles  W,  1;  Seneca,  li^  miles  NW,  1; 
Silver  Spring,  1;  Takoma  Park,  1;  Woodside,  5.  Prince  Georges 
County:  Bladensburg,  1;  Laurel,  9;  Oxon  Hill,  1.  District  of  Colu/m- 
hia:  61. 

Other  records  and  reports. — Allegany  County:  Green  Ridge  (Coll. 
U.  Md.).  Baltimore  County:  Bare  Hills-Lake  Roland  area  (Bures, 
1948:  68);  Patapsco  State  Park  (Hampe,  1939:  7).  Prince  Georges 
County:  Patuxent  Research  Center,  along  Patuxent  River  (Stickel, 
Lucille  F.,  1948 :  506). 

MUSKRAT 
Ondatra  zibethicus  macrodon  (Merriam) 

Fiber  macrodon  Merriam,  Proc.   Biol.   Soc.  Washington,   11 :   143, 
13  May  1897. 

336-897  O — 69 8 


110 


NORTH  AMERICAN;  FAUNA  66 


Type  locality. — Lake  Druminond,  Dismal  Swamp,  Norfolk  County,  Va. 

General  distribution. — Reported  from  Chester  County,  Pennsylvania,  south  in 
the  Coastal  Plain  and  Piedmont  to  the  lower  Cape  Fear  drainage  of  southeastern 
North   Carolina. 

Distribution  in  Maryland. — Eastern  Shore,  Western  Shore,  and 
Piedmont  sections. 

Muskrats  are  especially  abundant  in  the  fresh- water  and  brackish 
marshes  of  the  Eastern  Shore  section.  The  subspecies  incurr'odon  inter- 
grades  with  0.  z.  zihethlcus  in-  the  Piedmont  section  and  is  probably- 
replaced  by  that  subspecies  in  the  Ridge  and  Valley  and  Allegheny 
Mountain  sections. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  0/0,  3/3,  =  16; 
tail  long  and  laterally  compressed;  hind  feet  partially  webbed;  ears 
small  and  almost  hidden  in  fur;  pelage  dense,  underfur  soft  and  thick, 
overlaid  with  long  smooth  guard  hairs;  usual  coloration  a  rich  brown, 
with  considerable  bright  russet  to  red  tinge,  darker  on  head,  ncse, 
and  back;  Sides  grayish  brown  to  russet;  underparts  considerably 
lighter,  varying  from  grayish  drab  to  bright  cinnamon  rufous. 

There  is  a  black  color  phase  of  this  subspecies  which  in  some  Mary- 
land marshes  runs  as  high  as  65  percent  of  the  population  (Dozier, 
19486,  p.  393).  These  animals  are  not  unifoi-mly  black,  but  have  a 
modified  agouti  pattern  shown  in  the  lighter  ventral  surfaces  and  on 
the  lower  side  areas  where  the  hairs  are  subapically  banded  with 


Ondatra  zibethicrus 
•  Specimens  examined 
O  Specimens  reported 


Figure  40. — Distribution  of  Ondatra  zibcthicus. 


MAMMALS  OF  MARYLAND  lll\ 

yellow.  The  dorsum,  however,  is  a  uniform  glossy  black  with  no  hairs 
banded  with  red  and  yellow.  Rarely  an  albinistic  individual  is  encoun- 
tered, and  Dozier  (19486,  p.  394)  has  reported  upon  a  nonalbino  white 
mutation  ("Maryland  white")  occurring  in  some  of  the  marshes  in 
Dorchester  County,  and  fawn  colored  mutants  from  the  vicinity  of 
Chestertown,  Kent  County. 

The  muskrat  is  readily  distinguished  from  other  Maryland  rodents 
by  the  combination  of  its  aquatic  habits,  large  size,  and  laterally  com- 
pressed tail.  The  beaver,  which  the  muskrat  resembles  in  aquatic 
habits,  is  larger  and  has  a  broad,  horizontally  compressed  tail. 

Measurements. — External  measurements  of  an  old  male  and  two 
young  adult  females  from  Laurel,  Prince  Georges  County,  are  as  fol- 
lows: Total  length  675,  600,  570;  tail  280,  275,  266;  hind  foot  87,  86, 
79.  Cranial  measurements  of  11  adults  from  Laurel  are:  Condylobasal 
length  67.6  (63.9-72.2) ;  zygomatic  breadth  41.8  (39.8-44.5) ;  least 
interorbital  breadth  5.9  (5.0-6.6) ;  length  of  maxillary  toothrow  16.1 
(14.9-17.2). 

Dozier  et  al.  (1948,  p.  180)  found  that  the  average  weight  of  13,421 
male  muskrats  trapped  on  the  Blackwater  National  Wildlife  Refuge, 
Dorchester  County,  was  2  pounds  4  ounces,  and  the  average  weight  of 
10,090  females  was  2  pounds  2  ounces.  Adult  males  varied  in  weight 
from  6  ounces  to  4  pounds,  and  females  from  6  ounces  to  3  pounds  12 
ounces. 

Habitat  and  habits. — Muskrats  are  most  abundant  in  the  extensive 
marshes  that  line  the  Chesapeake  Bay.  Elsewhere  in  Maryland  they 
are  found  in  streams  that  wind  through  pastures,  and  in  swamps. 

The  muskrat  is  essentially  vegetarian,  but  occasionally  will  make 
use  of  animal  food  such  as  fish,  mussels,  insects,  crayfish,  and  snails. 
Martin  et  al.  (1951,  p.  236)  report  that  at  the  Patuxent  Research  Cen- 
ter near  Laurel,  the  most  important  plant  material  eaten  is  burreed, 
cutgrass,  arrowhead,  waterlily  and  panicgrass.  Smith  (1938,  p.  12) 
found  that  muskrats  in  Dorchester  County  would  eat,  to  some  extent, 
almost  any  plant  found  in  the  marshes  there.  Certain  fa  verities,  how- 
ever, form  their  staple  diet,  and  no  area  lacking  these  will  support  a 
large  muskrat  population.  Three  square  sedge  and  broadleaf  and  nar- 
rowleaf  cattails  constitute  four-fifths  of  the  animal's  diet,  and  all  parts 
of  these  plants  are  eaten  at  one  time  or  another  during  the  year.  Other 
foods  that  are  at  times  utilized  by  the  muskrat  in  the  Dorchester 
marshes  are  saltmarsh,  wild  reed,  saltgrass,  beak-rush,  spikerush,  big 
cordgrass,  wild  millet,  and  sweet  sedge.  Also  occasionally  eaten  are 
saltmarsh  fleabane,  marshmallow,  waterlily,  dodder,  iris,  waxmyrtle, 
small  pine  trees,  and  poison-ivy.  Smith  found  that  Dorchester  County 
muskrats  sometimes  consumed  turtles,  blue  crabs,  fish  (chiefly  sluggish 
kinds  such  as  carp) ,  salt-water  mussels,  and  possibly  dead  birds. 


112  NORTH  AMERICAN  FAUNA  66 

In  the  Maryland  marshes,  muskrats  are  active  at  all  hours,  in  the 
spring  and  throughout  the  summer. 

Muskrat  homes  are  of  two  general  types  depending  on  the  topog- 
raphy of  the  area  in  which  they  live.  In  the  uplands  they  dig  burrows 
into  the  banks  of  streams  and  other  bodies  of  water,  while  in  the 
marshes  they  build  dome-shaped  structures.  The  entrance  hole  to  a 
bank  burrow  is  always  below  the  normal  level  of  water.  The  burrow 
turns  upward  above  water  level  and  ends  in  a  nest  of  grass.  The  dome- 
shaped  structures  that  they  build  in  the  marshes  may  be  as  much  as  7  or 
8  feet  in  diameter  and  more  than  4  feet  high.  They  are  constructed  of 
stalks,  roots,  and  peaty  remains  of  plants  and  are  built  on  or  around  a 
firm  foundation  such  as  a  stump  or  the  base  of  a  tree.  Each  house  con- 
tains one  or  more  nests  from  which  passages  lead  to  plunge  holes  in  the 
floor.  These  holes  in  turn  lead  to  underground  tunnels  that  connect 
with  the  surface  several  feet  from  the  house. 

Muskrats  are  primarily  aquatic  and  construct  elaborate  canals,  6 
inches  to  a  foot  wide,  and  sometimes  a  foot  or  more  deep,  which  are  not 
visible  when  the  water  is  high.  Those  canals  which  are  used  as  main 
arteries  of  travel  are  always  wider  and  deeper  than  those  used  only 
as  temporary  leads  made  in  search  of  food.  In  dry  areas  the  muskrats 
use  surface  trails  concealed  in  the  grass  that  lead  in  all  directions,  and 
except  for  size,  resemble  those  made  by  the  meadow  mouse. 

In  addition  to  surface  canals  and  trails,  muskrats  construct  elaborate 
systems  of  underground  burrows  and  tunnels  that  spread  out  in  all 
directions  and  are  connected  with  the  surface  and  the  canals  by  plunge 
holes  scattered  at  convenient  intervals. 

Smith  (1938,  p.  16)  found  that  in  Maryland  the  muskrat  may  breed 
in  any  month  with  the  possible  exception  of  November  and  December. 
Most  of  the  young  are  bom  from  mid- April  to  mid-September.  Most 
Maryland  trappers  report  that  there  are  three  litters  a  year,  but  Smith 
(1938,  p.  16)  was  only  able  to  obtain  two  a  year  in  pen-raised  animals. 
The  number  of  young  is  variable ;  in  the  Maryland  investigations  con- 
ducted by  Smith,  the  number  averaged  4.4,  seven  being  the  most  found 
in  any  one  uterus.  The  gestation  period  appears  to  be  about  29  or  30 
days,  and  muskrats  probably  first  breed  at  the  age  of  1  year. 

The  population  of  muskrats  in  Maryland  marshes  apparently  has 
been  decreasing  since  1939.  The  number  of  muskrats  trapped  in  the 
marshes  from  year  to  year  may  not  reflect  the  actual  muskrat  popula- 
tion since  many  factors  such  as  food,  predation,  salinity,  and  breeding, 
which  are  not  readily  observable,  together  with  the  value  of  pelts,  act 
together  to  affect  muskrat  abundance,  and  may  be  different  from  year 
to  year.  Furthermore,  these  factors  may  cause  different  reactions  on  the 
part  of  the  muskrat  populations  at  different  levels  of  abundance. 
Nevertheless,  trapping  records  probably  give  an  adequate  index  of  the 


MAMMALS  OF  MARYLAND  113 

larger  fluctuations  in  population  level  in  Maryland.  With  this  in  mind, 
Harris  (1952,  p.  13)  lists  the  muskrat  catch  on  approximately  600  acres 
of  marsh  on  the  Nanticoke  River,  Dorchester  County.  In  193Y,  the 
total  catch  of  muskrat  on  this  marsh  was  2,417  animals  (4.0  animals 
per  acre).  By  1950  the  catch  on  this  same  marsh  had  dropped  to  150 
animals,  or  0.2  animals  per  acre.  On  a  Statewide  level,  the  total  catch 
of  muskrat  was  estimated  at  2  million  in  1938.  In  1949,  when  Maryland 
first  began  to  keep  accurate  records  of  the  muskrat  catch,  only  228,548 
animals  were  reported  trapped  throughout  the  State.  By  1957  this 
figure  had  dropped  to  a  low  of  112,348  muskrats.  The  1967-68  catch  was 
reported  as  139,000. 

These  figures  show  that  the  muskrat  population  has  been  experi- 
encing a  decline  over  the  past  25  years,  and  since  the  muskrat  is  an 
economically  important  animal,  there  has  been  considerable  specula- 
tion and  research  devoted  to  the  reason,  or  reasons,  for  this  decline. 
Hardy  (1950,  pp.  8-9,  27)  records  the  opinions  of  the  trappers  them- 
selves regarding  this  decline,  which  includes  such  ideas  as  there  being 
a  definite  ecological  relationship  between  muskrats  and  domestic  hogs. 
These  trappers  stated  that  with  the  fencing  in  of  property  in  Dor- 
chester County  the  hogs  were  no  longer  able  to  root  in  the  marshes 
and,  hence,  the  ecological  relationship  of  the  two  species  was  destroyed 
and  the  muskrat  population  declined.  Another  theory  maintained  by 
some  of  the  trappers  is  that  owing  to  various  causes  there  has  been  a 
great  increase  in  the  number  of  eels  in  Dorchester  County  waters  and 
that  eels  enter  the  muskrat  houses  and  consume  young.  Other  ideas  are 
that  the  muskrat  decline  is  due  to  increased  predation  by  raccoons 
and  foxes ;  a  "dreadful  disease" ;  floristic  changes ;  "trapping  under" 
(placing  the  tra,p  in  underground  leads) ;  and  high  water.  Hardy 
(1950,  p.  27)  notes  that  some  of  these  factors  may  have  been  operative, 
but  that  it  can  safely  be  assumed  that  the  diminishing  population  of 
the  muskrat  in  Dorchester  County  has  been  brought  about  by  a  com- 
bination of  ecological  and  environmental  changes  rather  than  by  any 
single  factor.  Harris  (1952,  p.  36)  points  out  that  his  study  on  Dor- 
chester County  muskrats  did  not  answer  the  question  why  there  has 
been  a  decline  in  their  numbers,  but  it  did  show  that  the  combination 
of  predation  and  a  reduced  capacity  of  the  marsh  to  support  muskrats 
may  prevent  a  rapid  increase  in  the  muskrat  population. 

Specimens  exaTnined. — Anne  Arundel  County:  Broadwater,  1.  Dor- 
chester County:  Blackwater  National  Wildlife  Refuge,  8.  Frederick 
County:  Jefferson,  1.  Montgomery  County:  Forest  Glen,  1;  Kensing- 
ton, 1 ;  Sligo  Branch,  1.  Prince  Georges  County :  Beaverdam  Creek,  1 ; 
Beltsville,  1;  Branch ville,  3;  Lanham,  2;  Laurel,  147.  District  of 
Colwmbia:  6. 


114  NORTH  AMERICAN  FAUNA  66 

Other  records  aTid  reports  (from  Dozier,  19486,  unless  otherwise 
noted). — BaltiTnore  County:  Bare  Hills-Lake  Roland  area  (Bures, 
1948,  p.  68)  ;  Loch  Raven  (Kirkwood,  1931,  p.  317)  ;  Patapsco  State 
Park  (Hampe,  1939,  p.  7).  Dorchester  County:  Best  Pitch  Ferry; 
Elliotts  Island;  Fishing  Bay;  Joe's  Point;  Robbins,  near;  Taylors 
Island;  World  End  Creek,  near  Golden  Hill.  Gai^rett  County:  Piney 
Run,  near  Piney  Dam  (trapping  record,  Maryland  Nat,  Res.  Inst.) ; 
Pawn  Run,  as  it  enters  Deep  Creek  (trapping  record,  Maryland  Nat. 
Res.  Inst.) .  Kent  County:  above  and  below  Chestertown,  on  the  Chester 
River;  Chestertown  (specimens  in  Acad.  Nat.  Sci.  Phila.  collection)  ; 
Fairlee  Creek  near  its  Chesapeake  Bay  Mouth.  Montgomery  County: 
Mainland  across  from  Plummers  Island  (Goldman  and  Jackson,  1939, 
p.  133).  Prince  Georges  County :  Patuxent  Research  Refuge  (Uhler  & 
Llewellyn,  1952,  p.  81).  Queen  Annes  County:  Booker's  Wharf. 

Remarks. — I  have  not  been  able  to  examine  specimens  from  the  Ridge 
and  Valley  and  the  Allegheny  Mountain  sections,  but  one  specimen  I 
examined  from  Jefferson,  Frederick  County,  just  to  the  east  of  the 
Blue  Ridge  Mountains,  is  clearly  an  intergrade  with  Ondatras,  zihethi- 
cu^  in  size  and  coloration,  and  almost  near  enough  to  typical  zibethicus 
to  be  assigned  to  that  subspecies.  On  the  basis  of  this  specimen,  and 
because  of  the  known  distribution  oi  O.  z.  zihethicus  in  Virginia  and 
Pennsylvania,  the  muskrats  of  the  Ridge  and  Valley  and  Allegheny 
Mountain  sections  probably  are  referable  to  the  subs,pecies  zibethicus. 
This  subspecies  appears  to  intergrade  with  the  Coastal  Plain  sub- 
species macrodon  throughout  most  of  the  upper  Piedmont  section. 

Published  reports  of  this  species  in  western  Maryland  are  by  Brown- 
ing (1928,  p.  213)  who  saw  muskrats  around  1825  in  the  vicinity  of 
Deep  Creek  Lake  in  Garrett  County,  and  by  Mansueti,  (1958,  p.  83), 
who  observed  them  in  Cranesville  Swamp,  Garret  County,  in  the 
1950's.  The  species  is  present  in  suitable  streams  and  ponds  through- 
out the  Ridge  and  Valley  and  Allegheny  Mountain  sections  at  the 
present  time,  and  according  to  Flyger  (in  verbis,  22  June  1964)  trap- 
pers report  that  they  are  not  uncommon. 

Ondatra  z.  zibethicus  differs  from  O.  z.  macrodon  in  its  darker 
pelage  (in  normal  color  phase),  and  in  its  smaller  size.  It  is  of  in- 
terest to  note  that  Merriam  in  his  original  description  of  macrodon 
(specimens  from  Dismal  Swamp,  Virginia)  considered  the  subspecies 
to  be  a  much  darker  form  than  zihethicus.  Merriam's  specimens,  how- 
ever, were  mostly  dark  phase  animals,  and  as  Hollister  (1911,  p.  18) 
has  shown,  macrodon  (in  normal  color  phase)  is  actually  a  lighter 
and  brighter  colored  subspecies  than  zibethicus. 


MAMMALS  OF  MARYLAND 


115 


SOUTHERN  BOG  LEMMING 
Synaptomys  cooperi  stonei  Rhoads 

Synaptomys  stonei  Rhoads,  Amer.  Nat.,  27 :  53,  January  1893. 

Type  locality. — ^May's  Landing,  Atlantic  County,  N.J. 

General  distribution. — ^Southern  Appalachians  of  eastern  Kentucky  and  Ten- 
nessee, western  North  Carolina  and  Virginia  and  western  Maryland  to  the 
Atlantic  Coastal  Plain  of  Maryland,  Delaware,  and  New  Jersey,  and  northward 
to  Connecticut  and  coastal  Massachusetts. 

Distribution  in  Maryland. — Statewide  in  distribution.  The  most 
southeasterly  record  for  the  subspecies  stonei  is  in  Worcester  County 
(Poole,  1943,  p.  103). 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  0/0,  3/3,  =  16;  size 
medium;  tail  short;  fur  rather  long  and  shaggy;  head  broad;  ears 
short,  rising  slightly  above  the  fur;  upper  incisor  teeth  grooved.  Color- 
ation of  upper  parts  brown  to  chestnut,  grizzled  in  appearance; 
underparts  silvery,  with  no  sharp  line  of  demarcation  on  the  sides; 
tail  grayish  black,  not  sharply  bicolored;  feet  brownish  black. 

This  is  the  only  short-tailed  mouse  in  Maryland  which  has  grooved 
upper  incisors,  and  may  thus  be  distinguished  from  all  others.  Crani- 
ally,  the  southern  bog  lemming  has  a  shorter  rostrum  than  any  other 
ISIaryland  mouse. 


79-                                                                   78' 

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Synaptomys  aooperi  stonei 
•     Specimens   examined 

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FiGUBB  41. — Distribution  of  Synaptomys  cooperi  stonei. 


116  NORTH  AMERICAN,  FAUNA  66 

Measurements. — External  measurements  of  five  adults,  and  cranial 
measurements  of  six  adults  from  Laurel,  Prince  Georges  County,  are 
as  follows :  Total  length  127.4  (120-135)  ;  tail  21.2  (18-23) ;  hind  foot 
19  (18-20);  greatest  length  of  skull  24.7  (24.3-24.9);  zygomatic 
breadth  17.0  (16.5-17.5)  ;  interorbital  constriction  2.9  (2.7-3.1) ;  length 
of  maxillary  toothrow  7.5  (7.4—7.8). 

Habitat  and  habits. — This  species  has  a  preference  for  sphagnum 
bogs,  and  this  is  where  most  Maryland  specimens  have  been  collected. 
It  is  sometimes  found,  however,  in  woodland  habitats,  including 
beach-maple,  oak-hickory,  and  pine.  Specimens  have  even  been  taken 
in  grassy  areas,  orchards,  weedy  fields,  and  marshes,  and  in  shocked 
corn. 

According  to  Conner  (1959,  p.  171)  the  chief  requirement  of  Synap- 
tomys  seems  to  be  the  presence  of  green  succulent  monocotyledonous 
plants,  primarily  sedges  and  grasses,  which  are  its  main  source  of 
food. 

This  species  may  breed  throughout  the  year,  although  Conner  (p. 
203)  found  that  in  southern  New  Jersey  there  was  a  spring  peak  in 
the  breeding  cycle,  with  some  breeding  continuing  through  summer 
and  autumn.  Poole  (1943,  p.  103)  found  a  lactating  female  in  Wor- 
cester County,  Md.,  in  late  November.  Conner  (p.  202)  found  that 
litters  of  from  two  to  five  were  usual  for  the  species,  although  a 
single  embryo  is  not  uncommon,  and  as  many  as  seven  young  have 
been  reported.  His  data  suggest  that  in  the  spring  and  summer  females 
produce  a  litter  every  67  days. 

Wherever  the  southern  bog  lemming  occurs,  it  is  found  in  com- 
pany with  other  small  mammals  such  as  red-backed  mice,  deer  mice, 
shrews,  and  moles,  and  it  often  occupies  the  same  burrows  as  these 
others.  The  nests  are  constructed  of  shredded  grasses  and  sedges 
and  are  often  concealed  some  distance  beneath  the  ground.  Less  often, 
they  are  placed  directly  on  the  ground  where  there  is  sufficient  ground 
cover.  Conner  (p.  227)  found  that  most  of  the  nests  in  southern  New 
Jersey  were  located  just  under  the  surface,  concealed  in  either  hemlock 
or  moss  or  in  other  elevated  mounds  in  the  bogs.  Most  of  the  nests 
were  balls  of  dry  shredded  leaves  of  sedge,  and  had  two  entrances. 
The  diameters  ranged  from  3i/^  to  6  inches,  and  the  hollow  spaces 
within  the  nests  ai^eraged  about  2i/^  inches. 

Specimens  examined. — Allegany  County:  Oldtown,  9  miles  E,  1. 
Prince  Georges  Coimty :  Beltsville,  1 ;  Beltsville,  21^  miles  W 
(sphagnum  bog),  5;  Hyattsville,  8.  District  of  Columhia:  1. 

Other  records  and  reports. — Montgomery  County:  Sandy  Springs 
[skull  removed  from  stomach  of  red-tailed  hawk]  (Bailey,  1923,  p. 
118) .  Worcester  County:  Snow  Hill,  6  miles  SW  (Poole,  1943,  p.  103) . 


MAMMALS  OF  MARYLAND  117 

Remarks. — The  specimen  from  9  miles  E  of  Oldtown,  Allegany 
County,  is  somewhat  smaller  in  size  and  less  grizzled  in  coloration 
than  those  from  farther  east  in  the  State.  This  animal  may  represent 
an  intergrade  in  these  characters  with  S.  c.  cooperi.,  the  subspecies  dis- 
tributed to  the  north  of  stonei,  or  may  actually  be  referable  to  that 
form.  As  Wetzel  (1955,  p.  12)  has  pointed  out,  however,  the  ranges 
of  all  measurements  in  these  two  subspecies  overlap,  and  the  variation 
in  coloration  within  only  one  sample  of  cooperi  for  one  season  is 
much  greater  than  between  the  various  subspecies  of  S.  cooperi.  This 
illustrates  the  difficulty  in  assigning  individual  specimens  to  sub- 
species. Because  of  this,  the  specimen  from  Allegany  County  is  pro- 
visionally assigned  to  S.  c.  stonei,  the  range  of  which  is  herein 
considered  to  encompass  the  entire  State.  When  more  specimens  from 
the  Piedmont  and  the  Ridge  and  Valley  sections  become  available  for 
study,  however,  it  may  be  found  that  S.  c.  cooperi  is  distributed  in 
those  sections,  and  that  the  specimen  from  Allegany  County  should 
properly  be  assigned  to  that  race. 

Family  CAPROMYIDAE  (hutias  and  coypus) 
NUTRIA 
Myocastor  coypus  (Molina) 

Mus  coypus  Molina,  Sagg.  Stor.  Natur.  Chili,  p.  287, 1782. 

Type  locality. — Rivers  of  Chile. 

General  distribution. — Ranges  widely  over  southern  SoutJi  America ;  intro- 
duced into  the  United  States  in  the  1930's,  and  now  is  established  in  the  wild 
in  at  least  16  states. 

Distribution  in  Maryland. — A  few  nutria  are  established  in  the 
Dorchester  County  marshes. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  1/1,  3/3,  =  20;  size 
large  (sometimes  attaining  a  weight  of  21  lbs.);  pelage  consisting  of 
2  types  of  hair,  dense  underfur,  and  long  glossy  overlying  guard  hairs; 
coloration  rich  brown  or  chestnut  on  dorsum,  paler  underneath;  tail 
long  and  cylindrical;  middle  toes  of  hind  feet  connected  by  a  basal  web. 

This  species  superficially  resembles  the  muskrat,  from  which  it  may 
be  readily  distinguished  by  its  larger  size,  cylindrical  as  opposed  to 
laterally  compressed  tail,  and  greater  number  of  teeth. 

Measurements. — An  adult  male  and  female  from  the  Blackwater 
National  Wildlife  Refuge,  Dorchester  County,  measure  externally  as 

follows :  Body  length  571, 518 ;  tail  413, ;  hind  foot  156, 137.  Dozier 

(in  correspondence)  reports  that  the  heaviest  animal  he  examined  at 
the  Fur  Animal  Experiment  Station  in  Cambridge,  Md.,  weighed  21 
pounds. 


118  NORTH  AMERICAN  FAUNA  66 

No  skulls  of  this  species  are  available  from  Maryland  for  measure- 
ment. 

Habitat  and.  habits. — The  habitat  of  the  nutria  in  its  South  Ameri- 
can home  is  in  marshes,  swamps,  and  along  the  margins  of  rivers  and 
lakes  in  fresh-water  plant  associations.  Bednarik  (1958,  p.  2)  says, 
however,  that  Randall  Rhodes,  Curator  of  Collections  at  the  Cleveland 
Museum  of  Natural  History,  has  told  him  (in  personal  communication 
1954)  that  in  South  America  he  observed  that  nutria  were  mostly  as- 
sociated with  marine  waters.  The  temperature  of  the  water  seems  to  be 
of  little  importance  to  them,  and  in  the  United  States  they  are  now 
found  as  far  north  as  Michigan  and  Washington  State,  where  they 
prosper  in  the  same  type  of  habitat  as  the  muskrat. 

The  nutria  is  a  vegeitarian,  consuming  a  variety  of  aquatic  plants, 
rushes,  reeds,  grasses,  seeds,  cattails,  and  sedges.  In  captivity  it  shows 
a  marked  preference  for  alfalfa  and  clover  and  is  fond  of  practically 
all  root  crops  except  Irish  potatoes.  Because  of  its  voracious  appetite 
it  has  posed  a  serious  threat  to  waterfowl  marshes  in  some  areas  where 
it  has  been  introduced. 

Nutria  li^ang  in  streams  or  ponds  which  have  steep  banks  burrow 
into  them  close  to  the  water  level.  Each  pair  makes  its  own  burrow, 
which  is  dug  in  and  upward  until  well  above  the  water  level.  The  den  is 
lined  with  grasses,  and  as  the  family  grows,  the  burrow  is  enlarged. 

If  the  nutria  are  living  in  a  marsh  which  does  not  have  steep  banks, 
floating  nests  of  aquatic  vegetation  are  built,  which  resemble  those 
made  by  the  muskrat.  Where  conditions  permit,  part  of  a  colony  may 
live  in  floating  nests  in  the  marsh,  while  other  animals  will  build  bank 
burrows. 

The  gestation  period  of  this  species  in  Maryland  is  between  130  and 
134  days  (Dozier,  unpublished  data,  U.S.  Fish  and  Wildlife  Service). 
The  young  seem  to  be  bom  during  all  seasons,  and  there  are  probably 
two  or  three  litters  a  year  per  female.  In  Louisiana,  litter  size  averages 
4.4  young  (Harris,  1956). 

Nutria  apparently  became  established  in  the  Dorchester  County 
marshes  of  Maryland  sometime  in  the  early  1940's.  There  are  no  rec- 
ords of  their  occurrence  there  earlier,  and  Herbert  L.  Dozier,  formerly 
Director  of  the  U.S.  Fur  Animal  Field  Station  at  the  Blackwater 
National  Wildlife  Refuge,  does  not  mention  their  presence  in  the  Mary- 
land marshes  in  his  extensive  nutria  correspondence  in  the  files  of  the 
Fish  land  Wildlife  Service  dating  back  to  the  period  13  March  1939,  to 
3  June  1941.  It  is  possible  that  Maryland's  nutria  population  may  have 
originated  as  escapees  from  the  U.S.  Fur  Animal  Field  Station,  al- 
though there  is  no  certain  proof  of  this.  In  the  late  1930's  and  early 
1940's  Dozier  was  conducting  experiments  at  the  Blackwater  Refuge 
on  the  feeding,  care,  and  breeding  of  captive  nutria.  In  one  of  his  le(t- 


MAMMALS  OF  MARYLANB  119 

ters  dated  18  November  1940,  now  in  the  files  of  the  U.S.  Fish  and 
Wildlife  Service,  he  says : 

We  have  recently  completed  two  new  large  100  sq.  ft.  inclosures  in  marsh  and 
pond  edge  and  have  released  a  pair  of  nutria  in  each  to  study  their  reactions  to 
various  types  of  local  habitat,  etc. 

There  is  no  record  of  what  became  of  the  inclosures  or  animals,  and 
Dozier  never  published,  to  my  knowledge,  the  results  of  his  study. 

Maryland  kept  no  accurate  records  of  its  annual  fur  catch  until  1949. 
Prior  to  that,  only  rough  estimates  were  made  each  year  as  to  the  num- 
ber of  animals  trapped  in  the  State,  and  no  mention  was  ever  made  of 
nutriia.  In  1949,  when  trappers  were  first  required  to  report  their 
catches,  four  nutria  were  among  the  animals  taken.  No  further  nutria 
were  reported  until  1956,  when  two  were  trapped  in  the  Dorchester 
marshes.  The  following  year  the  catch  was  45  and  in  1958  the  number 
had  risen  to  52.  Since  then  the  number  reported  has  declined.  Thirty- 
four  were  reported  for  1959,  none  for  1960,  and  five  in  1961.  It  appears 
that  nutria  in  the  Maryland  marshes  are  only  precariously  established. 

SpecimeMs  examined. — Dorchester  County:  Black  water  National 
Wildlife  Kefuge,  8. 

Family  MURIDAE  (Old  World  rats  and  mice) 

BLACK  RAT 

Rattus  rattus  (Linnaeus) 

[Mus]  rattus  Linnaeus,  Syst.  nat.,  ed.  10, 1 :  61, 1758. 

Type  locality. — Uppsala,  Sweden. 

General  distribution. — This  is  an  introduced  species.  In  the  United  States,  it  is 
well  established  and  abundant  in  the  south  Atlantic  and  Gulf  Coast  ports.  In  the 
northeastern  United  States  it  is  found  in  buildings  along  the  docks  of  some  sea- 
ports, and  at  several  isolated  inland  localities. 

Distribution  in  Maryland. — May  occur  at  present  in  some  buildings 
along  the  docks  in  Baltimore  City. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  0/0,  3/3,  =  16;  size 
medium;  general  build  slender;  muzzle  sharp;  ears  large,  almost 
naked,  reaching  or  covering  the  eyes  when  laid  forward;  tail  slender 
and  long,  at  least  as  long  as  the  combined  length  of  the  head  and 
body,  and  sometimes  longer;  pelage  soft,  but  covered  with  coarse 
guard  hairs,  giving  it  a  harsh  appearance. 

There  are  three  color  phases  of  this  species.  Some  authorities  have 
considered  these  as  distinct  subspecies  because  of  their  general  associa- 
tion with  distinct  geographic  areas.  One  of  these  color  phases,  known 
as  R.  r.  frugivorous.,  has  a  yellowish  or  reddish  brown  dorsum,  with  a 
white  or  yellowish  abdomen,  and  is  most  conunonly  encountered  in  the 
Mediterranean  area.  Another  color  variation,  R.  r.  alewandrinus^  has  a 


120  NORTH  AMERICAN  FAUNA  66 

brownish  dorsum,  similar  to  that  of  frugivorous^  but  with  a  gray 
venter,  and  is  most  abundant  in  the  Middle  East  and  North  Africa. 
The  third  color  phase,  known  as  R.  r.  rattus^  has  a  black  dorsum,  with 
a  dark  gray  venter,  as  in  alexandrinus^  and  is  mostly  associated  with 
the  cold  temperate  countries  of  northern  Europe.  In  general,  R.  r. 
frugivorous  is  a  wild-living  animal,  whereas  alexandrmus  and  rattus 
are  nearly  always  associated  with  man  and  his  habitations.  None  of 
these  varieties,  however,  is  exclusively  limited  to  any  of  the  geographic 
or  habitational  areas  mentioned  above,  and  all  three  forms  may  occur 
at  any  one  locality  or  in  any  one  habitat.  Because  of  this  it  seems 
advisable  at  present  to  consider  them  as  color  phases  rather  than  as 
distinct  subspecies  (Caslick,  1956,  pp.  255-257) .  All  of  the  color  phases 
may  be  encountered  in  the  United  States. 

Rattus  rattus  is  most  easily  confused  with  the  Norway  rat  {Rattus 
norvegicus) .  It  may  be  distinguished  from  that  species  by  its  smaller 
size,  more  slender  build,  more  elongated  nose,  larger  longer  ears,  and 
much  longer  and  more  slender  tail  (as  long  as,  or  longer  than,  the 
combined  length  of  the  head  and  body).  Cranially,  the  two  species 
differ  in  that  the  braincase  of  R.  rattus  is  shortened  and  rounded, 
whereas  that  of  R.  norvegicus  is  narrow  and  elongated,  the  well-devel- 
oped temporal  ridges  extending  parallel  to  each  other  for  a  consid- 
erable distance  on  each  side  of  the  cranium. 

Measuremsnts. — Two  adults  from  Washington,  D.C.  (taken  on  a 
river  boat  at  the  Seventh  Street  Wharf  on  23  April  1923)  measure 
as  follows :  Total  length  405, 423 ;  tail  218, 238 ;  hind  foot  37, 39 ;  great- 
est length  of  skull  43.6, 43.2 ;  zygomatic  breadth  20.8,  20.9 ;  interorbital 
constriction  6.4,  6.7;  length  of  maxillary  toothrow  7.0,  6.9. 

Habitat  and  habits. — This  rat  is  essentially  an  arboreal  animal  and 
seldom  inhabits  burrows.  Where  it  infests  buildings  and  houses,  it  is 
found  usually  in  the  walls,  ceilings,  or  roof,  but  seldom  in  basements  or 
in  sewers.  It  shuns  water  and  seldom  enters  it  voluntarily.  This  is,  how- 
ever, the  common  rat  on  ships,  to  which  it  gains  access  by  climbing 
the  moorings.  It  is  occasionally  introduced  with  shipments  of  grain  or 
fruit. 

In  diet,  the  black  rat  is  omnivorous,  consuming  a  wide  variety  of 
grains,  fruits,  vegetables,  and  animal  matter. 

The  species  is  polyestrous  all  the  year  round.  The  duration  of  ges- 
tation is  about  21  days,  and  the  average  litter  size  is  seven  to  nine. 

Black  rats  enter  into  close  relations  with  man  wherever  they  occur, 
and  for  this  reason  they  are  often  involved  in  the  transmission  of  dis- 
eases, principally  the  bubonic  plague. 

Specimens  examined. — District  of  Columbia:  Five  (three  taken 
on  river  boat  at  Seventh  Street  Wharf,  and  two  taken  in  the  Central 
Market  in  a  box  of  fruit  from  Egypt  in  February  1912) . 


MAMMALS  OF  MARYLAND  121 

Remarks. — It  is  generally  believed  that  the  black  rat  was  the  com- 
mon rat  of  the  eastern  United  States  before  the  late  18th  century. 
Around  that  time,  it  is  said,  the  Norway  rat  was  introduced,  and  be- 
cause it  is  a  larger  and  more  aggressive  animal  it  drove  the  black  rat 
out  except  near  shipping  ports  (see  Bailey,  1923,  p.  114).  There  is 
however,  no  real  evidence  that  the  black  rat  was  ever  well  established 
in  Maryland  or  in  any  other  Northeastern  State.  This  animal  prefers 
a  warm  climate  and  probably  found  Maryland  too  cold  for  its  liking. 
Moreover,  it  is  known  that  in  areas  in  the  South  the  black  rat  and  the 
Norway  rat  live  in  the  same  habitations  without  one  species  driving 
away  the  other.  In  areas  where  the  two  species  live  together,  however, 
there  seems  to  be  an  ecological  separation  in  that  the  black  rat  usually 
is  found  in  the  upper  stories  of  a  building,  while  the  Norway  rat  in- 
habits the  basement  and  adjacent  sewers  and  tunnels. 

At  the  present  time  there  are  no  known  colonies  of  this  species  in 
Maryland,  although  perhaps  a  few  animals  inhabit  some  of  the  build- 
ing along  the  docks  in  Baltimore  City.  In  1949  Davis  and  Fales  (1949, 
p.  248)  reported  them  present  in  only  three  Baltimore  buildings  and 
estimated  the  population  as  not  more  than  1,000.  This  rat,  however,  is 
the  common  ship  variety  and  probably  has  been,  and  will  continue  to 
be,  repeatedly  introduced  into  the  Baltimore  wharf  district. 

As  far  as  is  known,  none  are  established  now  in  Washington,  D.C., 
although  here  again  they  may  leave  boats  and  take  up  residence  in 
nearby  buildings.  Five  specimens  have  been  taken  in  the  District  of 
Columbia.  Three  of  these  were  removed  from  a  boat  that  had  docked 
at  the  Seventh  Street  Wharf  in  April  1923,  and  two  were  trapped  in 
January  and  February  of  1912  at  the  old  Central  Market,  to  which 
they  apparently  had  been  brought  in  baskets  of  fruit  from  Egypt. 

NORWAY  RAT 
Rattus  norvegicus  (Berkenhout) 

Mus  norvegicus  Berkenhout,  Outlines  of  the  natural  history  of  Great 
Britain  and  Ireland,  1 :  5, 1769. 

Type  locality. — England. 

General  Distribution. — This  is  an  introduced  form  that  has  become  widely 
established  throughout  North  America. 

Distribution  in  Maryland. — Statewide. 

Distinguishing  characteristics. — Similar  to  R.  rattus,  but  differs  in 
being  larger,  heavier,  and  shorter  tailed.  In  coloration  it  is  grayish 
or  reddish  brown  on  the  back,  heavily  lined  with  black  hairs  along  the 
middorsal  line.  The  belly  is  silvery  gray,  but  in  some  specimens  it  may 
be  washed  with  a  dingy  yellowish  -  brown.  Cranial  differences  between 
this  species  and  Rattus  rattus  are  described  under  the  latter  species. 


122  NORTH  AMERICAN,  FAUNA  66 

Young  Norway  rats  superficially  resemble  the  native  American  rice 
rats  {OryzoTnys  pahistris).  They  may  always  be  distinguished  from 
this  species,  and  from  other  cricetines,  by  the  upper  molar  teeth, 
which  in  the  genus  Rattus  ( and  in  the  other  introduced  Murid  genus 
Mus)  are  provided  with  small  rounded  cusps  (tubercles)  arranged  in 
three  longitudinal  rows  in  contrast  to  two  rows  of  longitudinal  cusps 
in  most  cricetines. 

Measurements. — An  adult  from  the  District  of  Columbia  measures 
as  follows:  Total  length  470;  tail  208;  hind  foot  43;  ear  21;  greatest 
length  of  skull  52.6;  zygomatic  breadth  27.6;  interorbital  breadth 
7.4 ;  length  of  maxillary  toothrow  7.3. 

Habitat  and  habits. — This  is  essentially  a  water-loving  and  burrow- 
ing animal.  In  the  spring  of  1963,  large  numbers  of  them  were  inhabit- 
ing burrows  in  the  banks  bordering  the  Loch  Raven  Reservoir  north 
of  Baltimore.  They  would  emerge  from  the  burrows  in  broad  daylight, 
dive  into  the  reservoir,  and  swim  considerable  distances  to  obtain 
scraps  of  bread  thrown  into  the  water  by  visitors  who  were  feeding 
the  numerous  carp  which  swim  in  the  area  near  the  dam.  In  Wash- 
ington, D.C.,  the  population  of  Norway  rats  has  recently  risen  to 
alarming  proportions.  Their  burrows  may  be  seen  around  many  of  the 
downtown  government  buildings  and  monuments,  and  at  dusk  they 
come  into  the  open  and  actively  forage  for  food  among  the  refuse 
and  rubble  left  by  tourists  during  the  day. 

The  city  of  Baltimore  has  always  had  a  Norway  rat  problem,  but 
these  animals  are  not  as  numerous  as  was  thought  at  one  time.  In  a 
careful  study  of  Baltimore's  rat  population  in  1949,  Davis  and  Fales 
(1950,  p.  146)  estimated  there  were  approximately  43,000  animals, 
with  a  range  of  from  26,000  to  68,000,  of  which  about  15,000  were  in 
commercial  areas.  They  had  estimated  that  the  population  in  1947 
was  165,000,  so  that  there  was  a  considerable  decline  in  the  period 
1947  to  1949.  With  improved  sanitation  and  methods  of  extermina- 
tion developed  during  the  intervening  years  it  may  be  assumed  that 
the  rat  population  of  the  city  at  present  is  no  higher,  and  probably 
lower,  than  in  1949.  Nevertheless,  rats  are  still  a  serious  economic  and 
public  health  problem  in  Washington  and  Baltimore. 

The  Norway  rat  is  known  to  occur  throughout  the  State  both  in 
commercial  buildings  and  habitations,  and  in  some  places  in  the  wild, 
particularly  in  the  summer. 

The  species  is  extremely  adaptable,  and  about  the  only  factor  essen- 
tial for  its  success  is  the  presence  of  water ;  it  drinks  freely,  and  is  a 
good  swimmer  and  diver.  It  will  eat  virtually  anything,  and  finds 
sewers  particularly  attractive  places  to  live  because  of  the  abundant 
water  supply  and  the  offal  usually  found  therein  upon  which  it  can 


MAMMALS  OF  MARYLAND  123 

feed.  From  the  sewers  it  will  readily  pass  into  buildings  where  it  may 
cause  considerable  damage. 

The  species  is  an  efficient  burrower,  and  out-of-doors  its  bank  bur- 
rows consist  of  winding  galleries  furnished  with  several  escape  holes. 
On  farms,  it  frequently  makes  burrows  in  manure  piles,  rubbish 
mounds,  wheat  stacks,  and  hay  ricks.  Many  Norway  rats  spend  the 
summer  months  in  fields  and  meadows,  and  at  the  approach  of  cold 
weather  migrate  into  towns  and  villages  where  they  seek  the  warmth 
of  commercial  buildings  and  other  habitations. 

The  gestation  period  in  the  Norway  rat  is  21  days.  Studies  in 
England  (Hinton,  1931,  p.  13)  indicate  that  the  average  number  of 
young  per  litter  is  eight  or  nine,  but  that  there  are  records  of  as  many 
as  23.  Usually  the  number  ranges  between  6  and  19,  and  the  females 
may  produce  five  or  six  litters  annually. 

It  is  generally  believed  that  the  Norway  rat  and  the  black  rat  are 
incompatible,  and  that  the  larger,  more  aggressive  Norway  rat  will 
drive  out  or  kill  the  smaller,  weaker  black  species  wherever  they  are 
occupying  the  same  area.  There  is  no  proof  of  this,  however,  and  there 
are  even  cases  known  where  the  two  species  have  lived  together  in 
the  confines  of  a  small  ship  (Jolin  Jones,  U.S.  Fish  and  Wildlife 
Service,  in  verbis) .  The  fact  that  they  only  infrequently  occur  together 
is  probably  the  result  of  their  preference  for  different  climatic  situa- 
tions. The  Norway  rat  is  essentially  a  northern,  cool  climate  animal 
and  prospers  in  the  temperate  regions  of  northern  Europe  and  North 
America.  The  black  rat  originated  in  warm,  semitropical  areas  and 
find  its  optimum  conditions  in  the  warm  Mediterranean  regions  and 
in  the  southern  portions  of  the  United  States.  It  seems  probable  that 
the  black  rat,  although  repeatedly  introduced,  has  never  been  firmly 
established  in  the  northeastern  United  States  and  that  the  Norway 
rat  has  been  the  common  house  rat  in  Maryland  since  early  colonial 
times. 

Speciments  examined. — Anne  Arundel  Oounty:  Fort  Meade,  1.  Bal- 
tvmore  City:  1.  Calvert  County:  Solomons  Island,  1.  Montgomery 
County:  Silver  Spring,  1  mile  N,  3.  District  of  Columbia:  77. 

HOUSE  MOUSE 
Mus  musculus  Linnaeus 

Mv^  musculus  Linnaeus,  Syst.  nat.,  ed.  10,  Vol.  1,  p.  62, 1758. 

Type  looality. — Uppsala,  Sweden. 

General  distribution. — This  is  an  old  world  species  that  has  been  introduced 
into  the  United  States  and  is  now  found  in  a  commensal  and  feral  state  through- 
out the  country. 


124  NORTH  AMERICAN,  FAUNA  66 

Distribution  in  Maryland. — Occurs  abundantly  as  a  commensal  or 
as  a  feral  animal  in  all  sections  of  the  State. 

Distinguishing  characteristics. — This  small  mouse  is  well  known 
and  needs  no  extensive  description.  The  upper  molar  teeth  of  the  house 
mouse  are  essentially  like  those  in  Rattus  rattus  and  R,  norvegimis., 
that  is,  with  three  rows  of  longitudinally  arranged  cusps.  This  distin- 
guishes the  species  from  all  other  Maryland  mice  of  small  size. 

Externally,  the  house  mouse  superficially  resembles  American  mice 
of  the  genera  Peromyscus  and  Reithrodontomys.  It  differs  from  Mary- 
land Peromyscus  externally  in  its  smaller  size  and  in  coloration.  In 
adult  pelage,  Peromyscus  is  generally  a  brownish  gray  in  coloration 
on  the  dorsum,  with  a  white  venter,  the  line  of  demarcation  between 
the  two  being  sharply  marked.  The  tail  also  is  distinctly  bicolored, 
darker  above,  pale  below.  In  the  house  mouse,  the  coloration  is  more 
grayish  and  the  abdomen  is  generally  paler  than  the  dorsum,  but  there 
is  no  sharp  line  of  demarcation  between  the  two,  the  abdomen  seldom 
being  pure  white  as  in  Peromyscus.  In  addition,  the  tail  of  the  house 
mouse  is  not  distinctly  bicolored. 

The  dorsum  of  the  juvenile  Peromyscus  is  colored  a  uniform  slaty 
gray,  which  is  totally  unlike  the  grizzled  gray  of  the  house  mouse,  and 
the  venter  is  a  snowy  white  as  in  adults,  with  a  sharp  line  of  demarca- 
tion between  the  two. 

Externally,  the  house  mouse  is  very  smiliar  in  appearance  to  the 
harvest  mouse  {Reithrodontomys  hwmulis) .  The  most  certain  way  of 
separating  the  two  species  is  through  an  examination  of  the  upper 
incisor  teeth.  In  Reithrodontomys  there  is  a  longitudinal  groove  which 
runs  the  length  of  each  incisor,  while  in  the  house  mouse  these  teeth 
are  smooth.  In  addition,  the  biting  edges  of  the  upper  incisor  teeth  of 
the  house  mouse  usually  are  notched,  and  the  tips  of  the  lower  incisors 
fit  into  the  notches  when  the  jaws  are  closed. 

Measurements. — Seven  adults  from  the  vicinity  of  Ocean  City, 
Worcester  County,  have  the  following  external  measurements :  Total 
length  149.3  (140-167) ;  tail  vertebrae  73  (58-88) ;  hind  foot  17.4 
(16-18).  Cranial  measurements  of  five  adults  from  the  vicinity  of 
Ocean  City  are:  Greatest  length  20.9  (19.8-21.8) ;  zygomatic  breadth 
11.0  (10.6-11.5) ;  interorbital  breadth  3.4  (3.3-3.6) ;  length  of  maxil- 
lary toothrow  3.2  (3.1-3.4). 

Habitat  and  habits. — This  is  a  very  plastic  animal,  and  it  has 
adapted  itself  to  a  wide  variety  of  habitats.  Like  the  black  rat  and 
the  Norway  rat,  it  is  most  often  encountered  in  or  near  human  habita- 
tions, but  is  also  found  in  the  wild  throughout  Maryland. 


MAMMALS  OF  MARYLAMD  125 

This  species  probably  is  of  Asiatic  origin.  It  is  efficient  at  climbing, 
jumping,  and  swimming;  and  it  will  eat  and  thrive  on  practically  any 
food  that  man  consumes.  Its  nest  is  made  of  soft  materials  and  is 
placed  in  any  convenient  location,  such  as  in  walls,  under  floors  and 
steps,  in  bookcases  or  furniture,  and,  in  the  wild,  under  logs  or  stones 
and  other  convenient  recesses. 

The  house  mouse  is  very  prolific.  It  attains  sexual  maturity  at  the 
age  of  3  months  and  the  breeding  season  is  of  long  duration.  The 
gestation  period  is  from  19  to  21  days,  and  the  number  of  young  per 
litter  is  usually  five  or  six.  The  young  are  born  blind  and  naked,  but 
they  mature  rapidly  and  are  able  to  leave  the  mother  in  about  3  weeks. 

When  these  mice  inhabit  houses  in  large  numbers,  they  do  consider- 
able damage  by  eating  large  quantities  of  food,  or  tainting  it  with 
their  droppings.  They  will  consume  linen  clothing  of  all  types,  gnaw 
on  books,  and  chew  holes  in  the  woodwork.  In  shops,  warehouses,  grain- 
eries,  and  on  farms,  they  are  usually  abundant  and  destructive. 

In  Maryland,  the  house  mouse  is  found  everywhere,  even  on  marshes 
and  dunes  of  the  Atlantic  outer  barrier  beaches. 

Specimens  exaTnined. — Allegany  County:  Green  Ridge,  1;  Mount 
Savage,  7.  Anne  Arundel  County:  Annapolis,  3  miles  NW,  1.  Calvert 
County :  Drum  Point,  1 ;  Plum  Point,  2 ;  Plum  Point,  2  miles  W,  6 ; 
Scientists  Cliffs,  2;  Solomons  Island,  %  mile  N,  11.  Charles  Coumty: 
Nanjemoy  Creek,  1 ;  Port  Tobacco,  4.  Howard  Cownty:  Long  Comer, 
2.  Montgomery  County :  Cabin  John  Bridge,  2 ;  Chevy  Chase,  3 ;  Forest 
Glen,  5 ;  Gaithersburg,  5  miles  NE,  1 ;  Kensington,  7 ;  Seneca  Creek, 
1 ;  Silver  Spring,  1  mile  N,  2.  Prince  Georges  County :  Beltsville,  near, 
1 ;  College  Park,  1 ;  Lanham,  1 ;  Laurel,  5 ;  Mitchellville,  1  mile  W,  9 ; 
Oxon  Hill,  6;  River  View,  1;  sphagnum  bog,  near  District  line,  1. 
Queen  Annes  County:  Parson  Island,  1.  Washington  County:  Fort 
Frederick  State  Park,  2.  Worcester  Cownty:  Ocean  City,  3;  Ocean 
City,  5  miles  S,  on  Assateague  Island,  3 ;  West  Ocean  City,  4.  DistHct 
of  Columbia:  83. 

Remarks. — Schwarz  and  Schwarz  (1943,  pp.  59-72)  reviewed  the 
species  and  suggest  that  all  house  mice  in  the  United  States  are  re- 
ferable to  two  commensal  subspecies  M.  m.  hrevirostris  and  M.  m. 
domesticus^i  the  latter  being  the  one  that  supposedly  occurs  in  Mary- 
land. In  all  probability,  however,  house  mice  have  been  introduced 
into  Maryland  from  many  different  areas  and  at  many  different  times. 
The  range  of  variation  in  size,  tail  length,  and  coloration  in  Maryland 
specimens  is  so  great  that  I  am  unable  to  assign  them  a  subspecific 
name. 

336-897  O— 69 9 


126  NORTH  AMERICAN.  FAUNA  66 

Family  ZAPODIDAE  (jumping  mice) 

MEADOW  JUMPING  MOUSE 
Zapus  hudsonius  americanus  (Barton) 

Difus  americanus  Barton,  Trans.  Amer.  Philos.  Soc,  4:  115,  1799. 

Type  locality. — Schuylkill  River,  a  few  miles  from  Philadelphia,  Pa. 

General  distribution. — Southeastern  Uuited  States,  east  of  central  Indiana, 
and  south  of  central  New  York,  southward  into  northern  Georgia. 

Distribution  in  Maryland. — Occurs  in  all  sections  of  the  State. 

Distinguishing  characteristics. — Teeth  1/1,  0/0,  1/0,  3/3,  =  18;  upper 
incisors  grooved;  tail  very  long,  blackish  above,  white  below  (not 
white  tipped) ;  hind  legs  greatly  elongated ;  pelage  short  and  coarse ; 
coloration  yellowish  orange,  suffused  with  blackish,  the  blackish 
particularly  concentrated  in  the  middorsal  area  and  generally  forming 
a  rather  broad  band  from  nose  to  tail;  coloration  of  underparts  white, 
sometimes  suffused  with  yellowish  orange. 

This  mouse  is  readily  distinguished  from  all  other  Maryland  mice, 
except  the  woodland  jumping  mouse  {Nafoeozajms  insignis),  by  its 
very  long  tail  and  powerful  elongated  hind  legs.  It  is  distinguishable 
from  Napaeozapus  by  the  presence  of  a  premolar  in  the  upper  jaw,  the 
absence  of  a  white  tail  tip,  and  the  more  yellowish  coloration  (as 
opposed  to  orange  in  Napaeozapus)  on  the  flanks. 

Measurements. — Measurements  of  three  adults  from  the  vicinity  of 
Seneca,  Montgomery  County,  are  as  follows:  Total  length  195,  194, 
194;  tail  120,  110,  110;  hind  foot  26,  28,  28;  ear  11,  10,  10;  greatest 
length  of  skull  21.6,  22.0,  22.7 ;  zygomatic  breadth  10.5,  10.9,  10.6 ;  in- 
terorbital  breadth  4.2,  3.9,  4.0 ;  length  of  maxillary  toothrow  3.6,  3.7, 
3.5. 

Habitat  and  habits. — ^Krutzsch  (1954,  pp.  349-472)  revised  this 
genus,  and  gathered  together  its  natural  history  data.  Most  of  the 
following  is  based  on  his  account. 

The  meadow  jumping  mouse  inhabits  thick  vegetation,  usually 
grasses  or  forbs,  or  both,  in  areas  near  running  water.  It  is  found  both 
in  woodland  and  farmland,  but  is  most  abundant  in  open  moist  areas. 
In  Maryland,  the  species  occurs  throughout  the  State  in  suitable 
habitat,  although  nowhere  does  it  seem  particularly  abundant,  except 
perhaps  on  Assateague  Island,  where  it  is  common  in  the  mixed  cord- 
grass  and  myrtle  back  of  the  ocean  dunes. 

The  species  is  cyclical  in  abundance,  being  more  numerous  in  some 
years  than  in  others.  It  is  ordinarily  a  nocturnal  animal,  appearing 
in  the  early  dusk  and  remaining  active  until  predawn.  Occasionally, 
individuals  will  be  active  during  daylight  hours.  Meadow  jumping 
mice  hibernate  in  the  winter.  It  appears  that  it  is  necessary  for  this 


MAMMALS  OF  MARYLAND 


127 


Zapus  hudsonius  americanus 
•  Specimens  examined 
O  Specimens  reported 


FiGUBB  42. — Distribution  of  Zapns  hudsonius  americanus. 


mouse  to  accumulate  a  certain  amount  of  fat  before  it  is  capable  of 
hibernation  (Hamilton  1935,  p.  193),  and  thus  those  taken  in  autumn 
are  usually  fat. 

Almost  invariably,  meadow  jumping  mice  hibernate  in  burrows  in 
which  nests  are  constructed  of  grass,  leaves,  or  other  vegetation. 
Grizzel  (1949,  pp.  T'^TS)  found  two  of  these  animals  hibernating  in 
woodchuck  dens  at  the  Patuxent  Research  Center  in  January  1948. 
One  animal  was  found  4  feet  from  the  entrance  to  the  burrow  and 
about  40  inches  below  the  surface  of  the  ground.  The  second  was 
found  in  another  burrow  5  feet  from  the  entrance  and  26  inches  below 
the  surface.  Both  animals  were  curled  up  in  the  center  of  large  leaf 
nests  and  well  insulated  from  the  cold. 

In  the  vicinity  of  Washington,  D.C.,  these  mice  remain  active  well 
into  November,  and  emerge  from  hibernation  in  early  April.  In  the 
Allegheny  Mountain  section,  and  the  Ridge  and  Valley  section,  the 
hibernation  period  is  more  prolonged.  Occasionally,  during  mild  spells 
in  midwinter  they  merge  from  their  burrows  and  become  active. 
Barbehenn  tells  me  that  he  collected  one  jumping  mouse  in  an  old 
orchard  with  honeysuckle  and  poison-ivy  ground  cover  near  Rock- 
ville,  Montgomery  County,  on  11  February  1960,  in  very  mild  weather. 

During  their  active  part  of  the  year,  meadow  jumping  mice  wander 
freely  and  seldom  make  well-defined  trails  or  runways.  They  con- 


128  NORTH  AMERICAN  FAUNA  66 

struct  nests  of  grass  and  leaves  under  logs  or  occasionally  in  a  clump 
of  shrubs  a  few  inches  above  the  ground. 

Krutzsch  (1954,  p.  428),  citing  various  investigators,  lists  the  fol- 
lowing foods  consumed  by  these  mice:  Insects,  berries,  seeds,  nuts, 
fruits  of  various  kinds,  and  roots.  It  has  been  noted  that  meadow 
jumping  mice  are  highly  insectivorous  (Quimby,  1951,  pp.  85-86). 

According  to  Krutzsch  (1954,  p.  429),  meadow  jumping  mice  com- 
mence to  breed  shortly  after  they  come  out  of  hibernation,  and  the 
breeding  season  is  prolonged  until  just  before  they  reenter  hiberna- 
tion in  the  autumn.  There  are  probably  two  litters  produced  each 
breeding  season,  and  the  number  of  young  per  litter  varies  from  three  to 
eight.  Bailey  (1923,  p.  120)  reported  a  specimen  from  Sandy  Springs, 
Montgomery  County,  taken  on  19  May  1906,  that  contained  six  large 
embryos.  The  gestation  period  is  approximately  18  days. 

Specimens  examined. — Allegany  County:  Dans  Mountain,  1.  Charles 
County:  Marshall  Hall,  1;  Newport,  2.  Garrett  County:  Cunningham 
Swamp,  4;  Finzel,  1.  Montgomery  County:  Cabin  John  Bridge,  2; 
Kensington,  1 ;  Rockville,  2  miles  W,  1 ;  Sandy  Springs,  2 ;  Seneca  % 
mile  N,  1 ;  Seneca,  3  miles  W,  2.  Prince  Georges  County :  Branchville, 
1;  Laurel,  8;  Patuxent  Research  Center,  2;  Tuxedo,  1.  Worcester 
County:  Ocean  City,  5  miles  S  (Assateague  Island),  1.  District  of 
Columhia:  7. 

Other  records  and  reports. — Baltimore  County:  Patapsco  State 
Park  (Hampe,  1939,  p.  7).  Montgomery  County:  Forest  Glen  (one 
seen  by  G.  S.  Miller  and  reported  by  Bailey,  1896,  p.  98).  Prince 
Georges  County:  College  Park  (Krutzsch,  1954,  p.  439) . 

Remarks. — According  to  Krutzsch  (1954,  p.  439),  specimens  from 
Maryland,  Virginia,  and  North  Carolina  are  more  nearly  average 
representatives  of  the  subspecies  americanus  than  are  those  from  the 
region  of  the  type  locality. 

WOODLAND  JUMPING  MOUSE 
Napaeozapus  insignis  insignis  (Miller) 

Zapus  insignis  Miller,  Amer.  Nat.,  25 :  742,  August  1891. 

Type  locality. — Restigouch  River,  New  Brunswick,  Canada. 

General  distribution. — Eastern  Canada,  from  Nova  Scotia,  New  Brunswick, 
and  Quebec  soutii  of  St.  Lawrence  River,  south  into  northeastern  Ohio,  northern 
West  Virginia,  and  western  Maryland. 

Distribution  in  Maryland. — Allegheny  Mountain  section ;  may  also 
occur  in  the  Ridge  and  Valley  section,  but  has  not  been  reported  from 
there  as  yet. 

Distinguishing  characteristics . — Teeth  1/1,  0/0,  0/0,  3/3,  =  16;  closely 
resembles  the  preceding  species,  but  somewhat  larger  in  size;  coloration 


MAMMALS  OF  MARYLAND 


129 


^ 


Napaeozapue  insigms  insigms 
#  Specimens  examined 


Figure  43. — Distribution  of  Napaeozapus  insignis  insignis. 


similar  to  that  of  Zapus,  but  with  a  more  brilliant  orange  on  flanks 
tail  grayish  above,  white  below,  with  a  distinct  whitish  tip;  upper 
incisors  grooved  as  in  Zapus;  only  3  molars  present  in  maxillary,  as 
opposid  to  3  molar  and  1  premolar  in  Zapus. 

Measurements. — Measurements  of  six  adults  (Coll.  U.  Mich.)  from 
5  miles  SE  of  Grantsville  (alt.  2,500  ft.),  Savage  River  State  Forest, 
Garrett  County,  are  as  follows:  Total  length  223  (215-230) ;  tail  134.7 
(130-138) ;  hind  foot  30  (29-31)  ;  ear  16.2  (16-17) ;  greatest  length  of 
skull  23.1  (22.2-23.7)  ;  zygomatic  breadth  12.1  (11.8-12.3) ;  interor- 
bital  breadth  4.5  (4.1^.7)  ;  length  of  maxillary  toothrow  3.6  (3.4-3.8). 

Habitat  and  habits. — This  species  prefers  the  moist,  cool  forests 
where  it  is  particularly  abundant  along  the  banks  of  mountain  streams. 
One  of  the  Maryland  specimens  was  taken  along  Muddy  Creek,  near 
Swallow  Falls,  in  a  Rhododendron  and  hemlock  forest  which  is  typical 
woodland  jumping  mouse  habitat.  Handley  and  Patton  (1947,  p.  184) 
found  that  in  Virginia  they  are  most  common  at  high  altitudes  among 
ferns,  blackberry,  and  St.-Johns-wort  in  clearings  surrounded  by 
forest.  The  woodland  jumping  mouse  is  seldom  found  in  open  meadows, 
fields,  or  marshes  where  this  is  no  heavy  forest  within  close  proximity. 

This  species  makes  no  well-defined  trails  or  runways,  but  utilizes 
the  burrows  of  moles  and  larger  shrews,  or  seeks  shelter  under  rotting 
logs  and  fallen  trees.  Nests  are  usually  placed  several  inches  below 


130  NORTH  AMERICAN  FAUNA  66 

the  ground  and  are  made  of  leaves  and  dry  grass.  Sometimes  the  en- 
trance to  the  nest  is  closed  when  the  animal  is  in  the  burrow. 

During  the  colder  months  of  the  year,  woodland  jumping  mice 
hibernate,  and  their  life  processes  are  reduced  to  a  mininum.  In  the 
autumn  they  eat  heavily  and  accumulate  large  stores  of  fat  on  the  body 
to  carry  them  over  the  long  period  of  hibernation.  Their  hibernation, 
deep  and  prolonged,  is  usually  half  of  the  year. 

Hamilton  (1941,  pp.  260-261)  lists  the  food  of  the  woodland  jump- 
ing mouse  as  insect  larvae  (particularly  lepidopterous  and  dipterous 
forms),  spiders,  small  soil  worms,  centipedes,  various  small  inverte- 
brates, small  seeds,  tiny  nuts,  small  green  leaves,  blueberries,  rasp- 
berries, and  fragments  of  Asplenium  fronds. 

This  species  normally  raises  but  one  litter  a  year.  The  gestation 
period  is  between  20  and  23  days,  and  from  two  to  six  young,  possibly 
eight,  comprise  a  litter ;  the  most  frequent  number  appears  to  be  five. 

Specimens  examined. — Allegany  County:  Dans  Mountain,  2.  Garrett 
County:  Finzel,  1 ;  Grantsville,  5  miles  SE  (Savage  River  State  For- 
est), 8  (Coll.  U.  Mich.)  ;  Muddy  Greek  Falls,  3  (Coll.  U.  Md.) ;  Swal- 
low Falls  State  Forest  (along  Muddy  Creek) ,  1. 

Remarks. — Although  Preble  (1899,  p.  35)  noted  that  the  specimen 
he  collected  at  Finzel  showed  no  approach  to  N.  i.  roanensis  (type 
locality:  Roan  Mountain,  N.C.),  it  is  my  opinion  that  this  specimen 
and  one  from  Swallow  Falls  State  Forest  and  eight  from  5  miles  SE 
of  Grantsville  show  traits  that  are  characteristic  of  roanensis.  They 
are  smaller  in  size  and  darker  in  coloration  than  typical  insignis,  and 
they  appear  to  represent  intergrades  with  roanensis.  However,  they 
are  closer  to  insignis  than  roanensis  in  these  characters  and  are  herein 
assigned  to  the  former  subspecies. 

Order  CARNIVORA  (flesh-eating  mammals) 

Family  Canldae  (dogs,  foxes,  etc.) 

COYOTE 

Canis  latrans  Say 

Canis  latrans  Say,  in  Long,  Account  of  an  exped.  ...  to  the  Rocky 
Mts.  .  .  .  ,1:168,1823). 

Type  locality. — Engineer  Cantonment,  about  12  miles  southeast  of  the  present 
town  of  Blair,  Washington  County,  Nebr.,  on  the  west  bank  of  the  Missouri 
River. 

General  distribution. — Distributed  primarily  west  of  Mississippi  River,  from 
Alaska  to  Central  America,  with  the  center  of  population  in  the  Great  Plains 
of  the  United  States.  The  species  has  recently  been  reported  from  a  number  of 
Eastern  States,  and  apparently  has  been  expanding  its  range  eastward.  Some  of 
the  eastern  populations,  however,  may  be  derived  from  animals  that  escape  from 
captivity,  particularly  those  populations  in  Southern  States. 


MAMMALS  OF  MARYLAND  131 


.'9. 

1 

76' 

V 

76° 

7V 

/ 

K/^^ 

r   / 

— 7- 
/ 

i 

A 

j 

i 

^x,  .v^ 

y 

^ 

H 

^/^ 

-a9«- 

-36*- 

SCALE 
0        10      20      30MILES 

c 

1. 

-39°- 

C<mis   Xatrana 
C     Specimens  examined 

4 

1 

1 
7j9» 

T7* 

1 

76* 

eoM 

FiGUBE  44. — Distribution  of  Canis  latrans. 

Distribution  in  Maryland. — May  be  expected  anywhere  in  the  State. 
See  discussion  in  Remarks  section. 

Distinguishing  characteristics. — Teeth  3/3,  1/1,  4/4,  2/3,  =  42; 
closely  resembles  a  small  police  dog,  but  with  shorter  legs,  a  bushier 
tail,  and  a  more  slender  muzzle.  Some  feral  dogs  are  so  similar  to 
coyotes  that  it  is  a  difficult  task  for  even  an  expert  to  distinguish  them. 
The  problem  is  further  compounded  because  the  coyote  and  dog  may 
interbreed  in  the  wild,  although  authentic  reports  of  such  crosses  are 
scarce.  There  does  not  appear  to  be  any  certain  way  to  distinguish 
coyote-dog  hybrids  from  pure  domestic  dogs. 

The  coyote  is  grayish  in  coloration,  and  the  dorsal  hairs  are  tipped 
with  black.  There  is  a  rusty  or  yellowish  tint  on  the  neck  and  along 
the  sides,  particularly  on  the  flanks.  The  head  is  grizzled  gray ;  the  ears 
brownish.  The  feet  are  fulvous,  and  the  throat  and  belly  white.  Since 
some  domestic  dogs  may  be  similar  to  this  in  coloration,  it  is  sometimes 
necessary  to  examine  the  skull  to  determine  the  species  of  the  animal 
in  question.  The  most  important  cranial  difference  between  the  two 
is  that  in  the  coyote  the  frontal  region  of  the  skull  is  alw^ays  flattened, 
whereas  in  the  dog  it  bulges  to  some  degree.  In  some  varieties  of  domes- 
tic dog  this  bulge  is  quite  pronounced,  in  others  it  is  less  so,  but  it  is 
generally  more  developed  than  in  the  coyote.  The  second  most  notice- 
able difference  is  found  in  the  rostrum,  which  is  slender  and  elongated 


132  NORTH  AMERICAN  FAUNA  66 

in  the  coyote  and  usually  shorter  and  more  blunt  in  the  dog.  In  addi- 
tion, the  tips  of  the  upper  canines  of  the  coyote  fall  below  the  level  of 
the  anterior  mental  foramina  when  the  jaws  are  closed;  in  the  dog 
they  terminate  above  these  foramina.  The  premolar  teeth  in  the  coyote 
are  generally  widely  space ;  in  the  dog  they  are  crowded.  The  ventral 
surface  of  the  mandibular  ramus  is  flattened  in  the  coyote,  whereas  in 
the  dog  it  is  generally  rounded.  Various  indexes  have  been  developed 
to  express  numerically  some  of  the  above-mentioned  cranial  differences 
(see  Howard,  1949,  p.  171 ;  Bee  and  Hall,  1951,  pp.  73-77 ;  Burt,  1946, 
pp.  61-62). 

Certain  specimens  exhibit  a  confusing  combination  of  dog  and 
coyote  characteristics.  These  animals  may  represent  hybrids,  but  the 
characteristics  of  known  hybrids  have  not  been  adequately  documented. 
Until  the  problem  of  hybridization  between  the  coyote  and  dog  is 
thoroughly  studied  it  seems  advisable  to  refer  any  questionable  speci- 
mens to  the  latter  species.  The  domestic  dog  is  one  of  the  most  variable 
animals  with  regard  to  its  physical  structure,  whereas  the  coyote  is 
a  very  uniform  one  (except  for  size).  Because  of  this,  it  is  possible  for 
the  domestic  dog  to  exhibit  some  coyote  traits  without  having  any  ad- 
mixture of  coyote  blood,  whereas  it  is  far  less  likely  that  a  coyote  would 
exhibit  dog  traits  without  some  dog  intermixture. 

In  the  field,  the  coyote  at  a  distance  may  resemble  a  gray  wolf  ( Canis 
Iwpus).  The  coyote,  however,  is  much  the  smaller  animal,  has  a  more 
yellowish  cast  to  the  pelage,  and  carries  its  tail  lower  when  running. 
The  skull  of  the  coyote  is  smaller  than  that  of  the  gray  wolf,  and  more 
lightly  built ;  the  teeth  are  much  smaller,  and  the  frontal  region  of  the 
skull  is  flat,  whereas  in  the  gray  wolf  it  is  bulging  as  in  the  domestic 
dog. 

Both  the  red  fox  and  the  gray  fox  are  less  doglike  in  general  appear- 
ance than  the  coyote,  and  both  are  considerably  smaller  in  size,  and 
different  in  coloration. 

Measurements. — Externally  the  coyote  ranges  in  total  length  from 
1,052  to  1,320  mm.  with  a  tail  vai-ying  from  300  to  394  mm.  The  hind 
foot  averages  between  177  and  220  mm.  (Hall  and  Kelson,  1959,  p. 
843) .  Animals  from  southwestern  localities  are  smaller  than  those  from 
farther  north,  and  males  are  larger  than  females. 

A  male  from  5  miles  northwest  of  Poolesville,  Montgomery  County, 
and  a  female  from  Cecil  County,  near  the  Delaware  State  line,  west 
of  Middlebury,  Del.,  have  the  following  cranial  measurements :  Condy- 

lobasal  length  180.4, ;  zygomatic  breadth  99.8,  87.8;  interorbital 

breadth  29.6, 31.5 ;  length  of  maxillary  toothrow  82.3, 78.7. 

Habitat  and  habits. — ^The  coyote  prefers  open  or  semiopen  country. 
Young  (Young  and  Jackson,  1951,  p.  11)  calls  the  coyote  an  "edge" 
animal,  and  believes  that  it  has  expanded  its  range  as  the  forested 


MAMMALS  OF  MARYLANiD  133 

areas  of  the  country  vanished  either  through  natural  means  such  as 
forest  fires  or  through  manmade  means  such  as  logging  etc.  With  the 
clearing  of  the  land  in  the  Northeastern  United  States,  the  coyote 
probably  found  habitat  there  to  its  liking,  and  has  extended  its  range 
eastward. 

The  habits  of  the  coyote  are  thoroughly  discussed  by  Young  and 
Jackson  (pp.  47-105).  The  following  is  compiled  primarily  from  their 
findings. 

The  home  of  the  coyote  is  usually  a  den  which  it  constructs  on  a  bank 
or  hillside,  in  wheat  or  com  fields,  under  houses,  shacks,  drainage 
pipes,  or  in  hollow  logs  in  thickets.  Often  the  animal  makes  use  of  a 
fox  or  skunk  den,  enlarging  it  to  suit  its  needs. 

As  a  rule,  coyotes  do  not  mate  for  life,  but  some  pairs  may  remain 
together  for  a  number  of  years.  There  is  evidence  that  the  female  may 
breed  when  she  is  1  year  of  age.  The  breeding  season  is  from  February 
to  March  or  April,  being  earlier  apparently  in  northern  than  in  south- 
ern latitudes  (Hamlett,  1938) .  The  gestation  period  is  60  to  63  days,  and 
females  have  been  known  to  deliver  as  many  as  17  to  19  young,  although 
5  to  7  is  the  usual  number. 

Sperry  (1941)  examined  the  stomachs  of  8,339  coyotes  from  western 
and  midwestern  localities  and  found  that  the  principal  food  of  the 
species  is  animal  matter,  of  which  more  than  90%  consists  of  mammals. 
In  addition  to  carrion  (25.1%),  the  chief  mammals  consumed  are  rab- 
bits (33.2%),  rodents  (17.5%),  domestic  livestock  (13.5%),  big  game 
mammals,  principally  deer  (3.6%),  and  miscellaneous  mammals  such 
as  skunks,  badgers,  weasels,  shrews,  moles,  foxes,  raccoons,  cats,  etc. 
(1%).  Birds  comprise  some  2.9%  of  the  coyote's  diet,  and  other  verte- 
brates 0.08%.  Insects  account  for  1%  of  the  diet,  and  vegetable  matter, 
principally  wild  fruit  and  cultivated  fruit,  some  1.7%.  These  percent- 
ages vary  according  to  seasonal  availability. 

Specimens  examined -Cecil  County:  Near  Delaware  line,  west  of 
Middletown,  Delaware,  1.  Montgomery  County.  Poolesville,  5  miles 
NW,  1. 

Rem/irks. — ^The  coyote  has  been  reported  from  nearly  all  of  the 
Eastern  States.  It  is  known  that  the  species  has  been  extending  its 
range  eastward.  Probably  the  coyotes  of  our  Northeastern  States  are 
a  result  of  the  natural  expansion  of  the  range  of  the  species.  On  the 
other  hand,  coyotes  have  been  introduced  accidentally,  or  on  purpose, 
into  some  of  the  Southeastern  States,  and  present  populations  in  those 
States  may  derive  from  these  artificial  introductions. 

The  first  coyote  discovered  in  Maryland  was  taken  on  5  February 
1921,  on  a  farm  5  miles  NW  of  Poolesville,  Montgomery  County. 
Jackson  (1922,  p.  187)  in  a  discussion  of  this  animal  says ; 


134  NORTH  AMERICAN,  FAUNA  66 

The  question  naturally  arises  as  to  how  a  coyote  reached  this  eastern  locality.  It 
is,  of  course,  impossible  to  say  definitely.  The  animal  probably  escaped  from  cap- 
tivity. Or  it  may  represent  an  extreme  eastern  extension  of  the  geographic  range 
of  coyotes.  There  is  no  direct  evidence  for  or  against  either  of  the  suppositions. 
It  is  known  that  the  range  of  the  coyotes  has  gradually  extended  northward 
and  eastward,  but  it  would  seem  hardly  probable  that  the  si)ecies  has,  as  yet, 
ingressed  a  region  as  far  east  as  central  Maryland. 

The  area  in  which  this  animal  was  taken  was  transversed  by  a  ma- 
jor east- west  arterial  highway  (U.S.  Route  40)  and  it  seems  highly 
likely  that  the  animal  was  brought  into  the  area  artifically.  This  view 
is  supported  by  the  fact  that  nearly  40  years  elapsed  before  another 
coyote  was  discovered  in  Maryland.  If  the  Montgomery  County  coyote 
really  represented  a  southward  or  eastward  extension  of  the  range  of 
the  species,  there  probably  would  have  been  at  least  occasional  reports 
of  their  presence  in  the  State  in  later  years.  As  it  is,  not  until  21  April 
1961  was  another  coyote  discovered  in  Maryland.  On  this  date,  a  coyote 
was  shot  in  Cecil  County  near  the  Delaware  border  by  employees  of 
the  Delaware  Board  of  Game  and  Fish  Commissioners.  Here  again, 
the  area  where  the  animal  was  shot  is  near  a  major  east- west  highway 
system  and  not  very  distant  from  the  cities  of  Baltimore,  Wilmington, 
and  Philadelphia.  It  seems  likely  that  the  animal  was  brought  east  as 
a  pet,  and  either  was  released  or  escaped  from  captivity.  On  the  other 
hand,  the  increasing  number  of  reports  of  coyotes  from  New  England, 
New  York,  and  other  Northeastern  States  make  it  more  probable  now 
than  it  was  40  years  ago  that  the  species  has  reached  Maryland  in  its 
natural  range  expansion.  It  is  still,  nevertheless,  impossible  to  say 
definitely. 

RED  FOX 

Vulpes  vulpes  fulva  (Desmarest) 

Canis  fidvus  Desmarest,  Mammalogie  .  .  .,  pt.  1,  p.  203,  in  Encyclo- 
pedie  methodique  .  .  .  1820. 

Type  Locality. — Virginia. 

General  distribution. — Most  of  the  Eastern  United  States,  from  southern 
Maine,  southern  Ontario  and  Wisconsin,  south  to  Alabama,  Georgia,  and  the 
Carolina®. 

Distribution  in  Marylomd. — Occurs  in  all  sections  of  the  State. 

Distinguishing  char(wteristiGS. — Dental  formula  as  in  Ccmis;  sim- 
ilar in  size  and  general  characteristics  to  a  small  dog;  nose  sharply 
pointed ;  ears  prominent  and  erect ;  tail  long  and  bushy,  fulvous,  but 
strongly  streaked  with  black,  and  always  with  a  white  tip ;  pelage  long 
and  soft;  coloration  rusty  on  face  and  occiput,  usually  mixed  with 
whitish ;  upper  parts  colored  bright  yellowish  red,  or  fulvous,  darker 
on  the  median  line,  with  the  rump  grizzled  with  whitish ;  cheeks,  chin, 


MAMMALS  OF  MARYLAND 

135 

79-                                                                 76- 

1                                                                        ' 

77" 

7,6- 

7fe 

^S 

-39.-                                      SCALE 

O        >0      20      30  MILES 

B 

-39°- 

VuVpes  vulpes  fulva 

#     Specimens   examined 

^^^^^^^ 

'^7Z(^%^: 

O    Specimens    reported 
-36*- 

^^ 

%i 

/%! 

1                                                     1 
79'                                           rp' 

T7* 

1 

76» 

flOM 

Figure  45. — Distribution  of  Vulpes  vulpes  fulva. 


throat,  and  a  band  down  the  abdomen  white ;  feet  and  outside  of  ears 
black. 

Cranially,  this  fox  differs  from  the  gray  fox  ( Urocyon)  in  that  the 
temporal  ridges  enclose  a  narrow  V  on  the  top  of  the  skull,  whereas 
in  the  latter  they  are  distinctly  lyrate  in  shape ;  the  upper  incisors  are 
lobed,  in  contrast  to  the  unlobed  condition  in  Urocyon. 

Measurements. — Three  adult  males  from  Montgomery  County  have 
the  following  external  measurements:  Total  length  1030,  1000,  995; 
tail  370,  372,  360;  hind  foot  170, 165, 160;  ear  83,  86,  85.  Cranial  meas- 
urements of  seven  adults  from  Montgomery  County  are  as  follows: 
Basal  length  139.7  (133.8-143.6)  ;  zygomatic  breadth  72.0  (69.7-74.0) ; 
postorbital  constriction  23.9  (22.0-28.8)  ;  alveolar  length  of  upper 
maxillary  toothrow  61.8  (59.5-63.4) . 

Females  average  smaller  than  males  in  size. 

Habitat  and  habits. — The  red  fox  is  cosmopolitan  in  its  distribution, 
except  that  it  is  not  generally  found  in  dense  forests  and  woods.  It 
prefers  rolling  farmland,  sparsely  wooded  areas,  brushlands,  and  dense 
weed  patches,  usually  in  the  vicinity  of  a  stream  or  lake. 

The  species  is  now  abundant  in  all  sections  of  the  State,  although 
at  one  time  it  apparently  was  not  found  here.  According  to  Mansueti 
(1950,  pp.  27-28),  the  early  American  settlers  hunted  the  gray  fox 
{Urocyon  cmereoargenteus) .  The  Indians  were  unanimous  in  claim- 
ing that  before  the  coming  of  the  Europeans  there  were  no  red  foxes 


186  NORTH  AMERICAN  FAUNA  66 

in  the  area.  Sometime  around  1650,  red  foxes  were  imported  from 
England  and  released  along  the  Eastern  Shore  of  Maryland.  These 
foxes  apparently  thrived  and  by  the  late  1670's  had  spread  down  the 
peninsula  into  Virginia.  Today  the  species  is  widely  distributed  in 
Maryland,  and  is  found  even  within  the  limits  of  metropolitan  areas 
such  as  Baltimore  and  Washington,  D.C.  Whether  the  fox  which  now 
occurs  throughout  the  State  is  the  variety  introduced  by  the  English, 
or  the  native  eastern  North  American  form  which  has  extended  its 
range  southward,  will  be  discussed  under  the  Remarks  section. 

The  red  fox  is  extremely  abundant  in  some  areas  of  the  State.  Ac- 
cording to  the  League  of  Maryland  Sportsmen  (Rally  Sheet  4(10), 
p.  6,  December  1946)  79  were  caught  in  a  5-week  period  at  Mount 
Savage,  Garrett  County,  in  1946.  At  the  eastern  end  of  the  State  on 
the  outer  barrier  beach  of  Assateague  Island,  it  is  also  abundant,  and 
does  some  damage  to  nesting  birds  and  their  eggs.  This  species  still 
roams  in  Rock  Creek  Park  in  the  heart  of  Washington,  D.C. 

The  food  of  the  red  fox  varies  from  season  to  season.  Llewellyn  and 
Uhler,  (1952,  p.  198)  found  that  in  their  Maryland  sample,  compris- 
ing mostly  November,  December,  and  January  animals,  17  percent  of 
the  food  was  plant  material  consisting  of  fruits,  berries,  and  other 
plant  items.  Persimmon,  pokeberry,  and  wild  grape  were  most  often 
consumed,  while  in  the  fall  beechnuts  were  heavily  utilized.  Apple, 
pear,  and  com  were  eaten  to  a  minor  extent.  The  bulk  of  the  red  fox's 
food  consists  of  animal  foods,  the  most  important  part  of  which  ap- 
pears to  be  rabbit.  Also  consumed  are  rodents  (meadow  mice,  musk- 
rats,  pine  mice,  gray  and  flying  squirrels,  house  mice)  and  shrews. 
Birds  and  occasionally  insects  are  eaten.  In  the  spring  and  summer 
months  the  food  consists  of  woodchucks,  poultry,  rabbits,  small  ro- 
dents, birds,  snakes,  turtles,  eggs  and  varying  amounts  of  vegetable 
matter  particularly  raspberries  and  blackberries.  There  is  no  question 
that  red  foxes  prey  to  some  extent  on  domestic  livestock,  particularly 
poultry  when  it  is  not  properly  housed.  Sometimes  red  foxes  may  be- 
come quite  bold.  Vernon  Bailey  (unpublished  report  in  files  of  U.S. 
Fish  and  Wildlife  Service,  25  April  1936)  tells  of  a  pair  raiding  the 
henhouse  of  a  farm  in  Brookville,  Montgomery  County;  they  were 
so  bold  that  they  often  raided  in  broad  daylight  and  took  the  hens 
before  the  eyes  of  their  owners. 

The  red  fox  is  monogamous  and  is  believed  to  remain  mated  for 
life.  The  species  is  monestrous,  with  one  season  a  year.  Most  matings 
take  place  in  late  January  or  February,  and  the  gestation  period  is 
between  49  and  55  days.  Litter  size  varies  between  one  and  eight,  with 
four  or  five  being  the  usual  number. 

The  breeding  or  family  den  of  the  red  fox  is  nearly  always  in  a 
burrow,  often  that  of  a  woodchuck,  and  is  more  often  located  in  more 


MAMMALS  OF  MARYLAND  137 

open  land,  such  as  a  pasture,  fence  border,  or  cultivated  field.  Vernon 
Bailey  (unpublished  report,  1936)  described  one  such  den  at  Brooke- 
ville  as  follows : 

The  den  had  four  openings,  or  doorways,  10,  15,  and  20  feet  apart,  really  the  old 
doorways  of  a  woodchuck  den  enlarged  to  fox  size.  Two  opened  out  on  each  side 
of  a  big  chestnut  log,  3  or  4  feet  in  diameter.  The  burrows  had  been  dug  out 
by  the  foxes  to  about  twice  the  diameter  of  the  woodchuck  burrows  and  en- 
larged to  a  comfortable  fox  nest  room  20  feet  back  from  the  main  entrance  and 
10  feet  back  from  the  other  doorways.  They  ran  3  or  4  feet  below  the  surface 
through  hard  clay  full  of  rocks  that  necessitated  many  crooks  and  turns  but  ran 
uphill  so  the  nest  chamber  was  actually  higher  up  than  the  actual  doorway.  All 
of  the  burrows  centered  at  the  nest,  beyond  which  the  original  woodchuck  burrow 
extended  about  10  feet  further  but  did  not  come  to  the  surface. 

There  was  no  nest  material  in  the  nest  chamber,  but  semidry  earth  made  a 
comfortable  bed  for  the  young  foxes  with  their  dense  woolly  coats,  and  a  uniform 
temperature  that  I  should  guess  was  around  55°  F.  gave  them  a  healthy  home  in 
the  den. 

Both  parents  hunt  for  food  to  provide  for  the  young.  Bailey  de- 
scribes the  food  found  in  the  den  at  Brookeville : 

Much  food  had  been  brought  into  the  den  by  the  parent  foxes.  One  white  rooster 
had  been  all  eaten  but  the  wings  and  head  and  telltale  feathers  scattered  around 
the  doorway ;  one  large  house  rat  was  lying  near  the  doorway  and  two  others 
were  found  in  the  nest  chamber  and  parts  of  four  others  in  the  pantry,  an 
excavation  half  full  of  food  at  one  side  of  the  upper  entrance.  It  was  about  four 
feet  below  the  surface  and  so  cool  that  all  of  the  meat  was  fresh  though  some 
of  it  several  days  old.  From  this  were  taken  out  part  of  a  cottontail,  half  a 
crow,  and  a  mouse. 

Specimens  examined. — Arnie  Arundel  County:  Fort  George  G. 
Meade,  1;  Priest  Bridge  (near),  1.  Clmrles  County:  Waldorf,  1. 
Dorchester  County:  Blackwater  National  Wildlife  Refuge,  9.  Fred- 
erick County:  Jefferson,  2.  Garrett  County:  Oakland,  1.  Howard 
Coumty:  no  exact  locality,  1.  Montgomery  County:  Bethesda,  1; 
Brookeville,  1 ;  Fairland,  1 ;  Poolesville,  5  miles  SW,  3 ;  Potomac,  1 ; 
Eockville,  1 ;  Sandy  Spring,  1 ;  no  exact  locality,  1.  Prince  Georges 
County:  Laurel,  5;  Patuxent  Research  Center,  4.  Worcester  Coumty: 
Ocean  City,  3  miles  S  (Assateague  Island),  2.  District  of  Columbia:  3. 

Other  records  and  reports. — Allegany  County:  Mount  Savage 
(League  of  Maryland  Sportsmen,  Rally  Sheet  4(10),  p.  6,  December 
1946).  Baltimore  County:  Loch  Raven  (Kolb,  1938) ;  Patapsco  State 
Park  (Hampe,  1939,  p.  6).  Garrett  Ccmnty:  Finzel  (E.  A.  Preble  in 
field  report).  Montgomery  County:  Laytonsville  (rabid  red  fox  re- 
ported in  Washington  Evening  Star,  28  December  1956) ;  Plummers 
Island  (Goldman  and  Jackson,  1939,  p.  132). 

Remarks. — It  is  well  established  that  the  red  fox  was  either  scarce 
or  did  not  occur  in  Maryland  prior  to  the  colonization  of  the  State 
by  Europeans.  Churcher  (1959,  p.  514)  states  that  "a  red  fox  was  native 


138  NORTH  AMERICAN,  FAUNA  66 

to  Nor^.h  American  north  of  Lat.  40°  N  or  45°  N,  but  was  either  scarce 
or  absent  from  most  of  the  unbroken  mixed  hardwood  forests  (to  the 
south  of  this)  where  the  gray  fox  was  paramount." 

The  early  Maryland  colonists  originally  hunted  the  gray  fox,  but 
apparently  at  a  very  early  date  the  European  red  fox  was  imported  for 
hunting  purposes  and  was  released  at  various  localities,  one  of  which 
was  the  Eastern  Shore.  Since  the  red  fox  is  now  found  throughout  the 
whole  of  Maryland,  as  well  as  much  of  the  Southeastern  United  States, 
the  question  arises  whether  these  southern  red  foxes  are  the  European 
variety  or  native  North  American  red  foxes  which  have  extended  their 
range  southward. 

Churcher  (1959,  pp.  513-520)  has  established  that  the  European  red 
fox  and  the  North  American  red  fox  are  subspecies  of  the  same  species 
Vulpes  vulpes^  the  various  subspecies  intergrading  in  several  major 
characters  (shape  of  upper  first  molar,  breadth  of  rostrum,  develop- 
ment of  sagittal  crest)  from  western  Europe,  through  Siberia,  Alaska, 
Canada,  to  eastern  North  America.  The  two  end  products,  the  west- 
ern European  red  fox  and  the  eastern  North  American  red  fox  are, 
however,  quite  different  animals  even  if  only  subspecifically  distinct. 
The  European  red  fox  is  larger  and  has  a  more  robust  skull  than  its 
eastern  American  relative.  It  also  has  a  shorter,  broader  rostrum, 
a  relatively  narrower  interorbital  region,  and  a  well-developed  sagittal 
crest  which  forms  a  distinct  ridge  along  the  top  of  the  skull.  In  the 
native  eastern  American  red  fox  the  sagittal  crest  is  occasionally  de- 
veloped but  usually  not  into  a  conspicuous  ridge.  It  narrowly  diverges 
anteriorly  into  the  temporal  ridges  which  enclose  a  conspicuous  V  on 
the  top  of  the  skull.  This  conspicuous  V  formed  by  the  temporal  ridges 
is  usually  not  as  well  developed,  or  is  lacking,  in  the  European  form. 
The  shape  of  the  first  upper  molar  also  differs  in  the  two  subspecies. 
In  the  European  variety  this  tooth  is  large  and  square  in  general  out- 
line, the  buccal  cingulum  is  rounded,  the  talon  broad,  and  the  mesial 
face  convex.  In  the  American  form,  the  tooth  gives  the  general  appear- 
ance of  being  elongated  laterally ;  the  buccal  face  is  deeply  indented, 
the  talon  elongated,  the  mesial  and  distal  faces  concave,  and  there  is 
a  small  protoconule. 

All  the  Maryland  red  foxes  (and  those  from  farther  south)  that  I 
have  examined  show  the  characters  of  the  native  eastern  North  Amer- 
ican  form,  and  there  seems  to  be  no  indication  of  intermixture  with 
European  fox  blood.  In  fact,  Maryland  specimens  appear  to  be  indistin- 
guishable from  those  of  Wisconsin,  Michigan,  southern  Ontario,  and 
New  England,  where  I  presume  there  was  little  or  no  importation  of 
European  stock  by  early  colonists.  It  is  possible  that  with  the  clearing 
of  land  in  the  Southeastern  United  States,  the  habitat  became  well 
suited  to  the  native  American  red  fox,  which  then  invaded  the  area 


MAMMALS  OF  MARYLAMD  139 

from  the  north.  The  European  red  foxes,  which  may  never  really 
have  been  well  established  in  the  United  States,  were  perhaps  swamped 
by  the  influx  of  native  American  foxes  and  left  no  recognizable  char- 
acteristics on  the  present  fox  population  in  Maryland  or  elsewhere  in 
the  Southeast. 

GRAY  FOX 
Urocyon  cinereoargenteus  cinereoargenteus  (Schreber) 

Cards  cinereo  argenteus  Schreber,  Die  Saugtheire  .  .  .,  Thiel  2,  Heft 
13,  pi.  92, 1775. 

Type  locality. — Eastern  North  America. 

General  distribution. — Distributed  from  southern  New  York  and  Lower 
Peninsula  of  Michigan,  south  to  South  Carolina  and  Tennessee,  west  to  eastern 
Illinois. 

Distribution  in  Maryland. — Occurs  in  all  sections  of  the  State.  It  is 
more  abundant,  however,  in  the  rolling  hilly  country  of  the  Piedmont, 
Ridge  and  Valley,  and  Allegheny  Mountain  sections  than  in  the  low, 
flat,  mashy  country  of  the  Eastern  Shore  section. 

Distinguishing  characteristics. — Dental  formula  as  in  Canis;  colora- 
tion grizzled  gray  above  with  hairs  banded  with  black  and  grayish 
white ;  inner  sides  of  legs,  sides  of  belly,  neck,  and  band  across  chest 
reddish  brown ;  belly  and  throat  white ;  chin  black ;  underf ur  soft  and 
wooly,  overlaid  with  short,  coarse  guard  hairs;  tail  bushy,  laterally 
compressed  with  a  concealed  mane  of  stiff  black  hairs  on  its  upper  side, 
near  the  base;  legs  short,  feet  equipped  with  well-curved  claws  that 
adapt  the  animal  for  climbing;  skull  with  temporal  ridges  whose 
divergent  branches  enclose  a  lyrate  area  and  never  coalesce  to  form  a 
distinct,  sharp  central  sagittal  crest. 

This  fox  is  somewhat  smaller  in  size,  has  shorter  legs,  and  is  differ- 
ently colored,  than  the  red  fox. 

Measurements. — An  adult  male  from  Washington,  D.C.,  has  exter- 
nal measurements  as  follows:  Total  length  996;  tail  356;  hind  foot 
143 ;  ear  71.  The  animal  weighed  lOi/^  lbs. 

Six  adults  of  both  sexes  from  Laurel,  Prince  Georges  County,  have 
the  following  cranial  measurements:  Basal  length  112.7  (110.8- 
114.0) ;  zygomatic  breadth  67.0  (63.0-70.8) ;  interorbital  breadth 
24.9  (23.8-27.3) ;  alveolar  length  of  maxillary  toothrow  51.6  (50.9- 
52.9). 

There  does  not  appear  to  be  any  appreciable  size  difference  between 
the  sexes. 

Habitat  and  habits. — This  animal  is  essentially  a  southern  and  west- 
ern species  that  has  apparently  only  recently  invaded  this  northern 
portion  of  its  range  (Hamilton  1943,  p.  176).  It  prefers  timbered  and 
rocky  regions.  Because  of  its  relatively  short  legs,  it  has  no  great 


140 


NORTH  AMERICAN  FAUNA  66 


Urooyon  cinereoargenteus  ainereoargenteu. 
•  Specimens  examined 
O  Specimens  reported 


Figure  46. — Distribution  of  Vrocyon  cinereoargenteus  cinereoargenteus. 


speed  and  would  perhaps  have  difficulty  surviving  in  wide  open  areas. 
On  the  other  hand,  it  is  quite  at  home  in  the  trees,  being  more  arboreal 
than  the  red  fox.  For  protection,  it  depends  to  some  extent  on  rocky 
or  brushy  cover  to  which  it  can  retreat,  or  forests  where  it  can  quickly 
climb  a  tree  to  escape  a  predator.  Of  60  gray  foxes  trapped  at  the 
Patuxent  Research  Center,  Prince  Georges  County,  in  the  1940's,  the 
majority  were  taken  in  hedgerows  and  margins  habitat,  and  most  of 
the  others  in  bottomland  forests  (Uhler  and  Llewellyn,  1952,  p.  84). 

This  species  selects  a  hollow  tree  or  log  for  a  den ;  occasionally  it 
may  use  a  burrow  in  the  ground.  It  breeds  but  once  a  year,  usually  in 
February.  Young  are  born  from  March  to  May  and  may  number  from 
two  to  seven,  with  the  average  being  four.  Both  parents  take  part  in 
caring  for  the  young. 

The  food  of  the  gray  fox  varies  from  season  to  season.  Studies  at 
the  Patuxent  Research  Center  (Llewellyn  and  Uhler,  1952,  p.  199) 
indicate  that  in  late  fall  and  early  winter  approximately  30  percent  of 
the  gray  fox's  food  is  plant  material,  while  about  70  percent  is  animal. 
Of  the  plant  food  consumed,  persimmon  was  the  most  important  item, 
while  corn,  pear,  apple,  and  beechnut  were  also  taken.  Rodents  were  by 
far  the  most  important  animal  food,  but  rabbits,  birds,  and  insects  were 
also  consumed.  Hamilton  (1943,  p.  177)  lists  rabbits  as  the  most 
important  food  for  the  species.  He  also  lists  birds,  small  mammals, 


MAMMAI/S  OF  MARYLAND  141 

particularly  field  mice,  deer  mice,  wood  rats,  and  shrews,  snakes,  tur- 
tles, and  their  eggs,  lizards,  insects,  apples,  beechnuts,  corn,  grapes, 
hickory  nuts,  persimmons,  carrion,  wild  cherries,  and  grasses  as  addi- 
tional food  items. 

The  species  is  abundant  in  the  Piedmont,  Ridge  and  Valley,  and 
Allegheny  Mountain  sections.  Forty  gray  foxes  were  taken  in  only  5 
weeks  in  1946  at  Mount  Savage,  Garrett  County  (League  of  Mary- 
land Sportsmen,  Rally  Sheet  4(10) ,  p.  6,  December  1946).  The  species, 
however,  is  not  abundant  in  the  Eastern  Shore  section.  In  fact,  the 
first  gray  fox  ever  taken  on  the  Blackwater  National  Wildlife  Refuge, 
Dorchester  County,  was  obtained  as  late  as  22  October  1943.  Appar- 
ently much  of  the  Eastern  Shore  section  is  too  low,  flat,  and  marshy 
for  the  animals'  liking. 

Specimens  exammed. — Anne  Arundel  County:  Fort  George  G. 
Meade,  1.  Charles  County:  La  Plata,  1;  Rock  Point,  1.  Dorchester 
County:  Blackwater  National  Wildlife  Refuge,  1  (baculum).  Mont- 
gomery County:  Plummers  Island,  1;  Silver  Spring,  1.  Prince 
Georges  County:  Beltsville,  1;  Berwyn,  2;  Landover,  1;  Largo,  1; 
Laurel,  11 ;  Marlboro,  1. ;  Oxon  Hill,  1 ;  Patuxent  Research  Center,  11. 

Other  records  and  reports. — Allegany  County:  Mount  Savage 
(League  of  Maryland  Sportsmen,  Rally  Sheet  4(10),  p.  6,  December 
1946).  Montgomery  County:  Cupids  Bower  (Bailey,  1923,  p.  123.). 

Family  URSIDAE  (bears) 

BLACK  BEAR 
Vrsus  americanus  Pallas 

Ursus  aTnericanus  Pallas,  .  .  .  Spicilegia  zoologica,  .  .  .  fasc.  14:  5, 
1780. 

Type  locality. — Eastern  North  America. 

General  distribution. — Wooded  areas  of  North  America,  from  Newfoundland 
to  Alaska,  and  south  into  central  Mexico. 

Distribution  in  Maryland. — The  black  bear  was  once  distributed 
throughout  the  State,  but  today  is  on  the  verge  of  extirpation  and  is 
found  only  in  restricted  areas  in  the  Ridge  and  Valley  and  Allegheny 
Mountain  sections. 

Distinguishing  characteristics. — Teeth  3/3,  1/1,  4/4,  2/3,  =  42; 
largest  wild  mammal  in  Maryland;  toes  armed  with  strong  claws; 
normal  color  both  above  and  below  black  or  very  dark  brown,  except 
for  cinnamon  patch  across  muzzle  and  sometimes  a  white  blotch  on 
throat;  pelage  harsh  and  coarse.  The  black  bear  is  so  familiar  as  to 
scarcely  need  description. 

Mea^ureinents. — "Total  length,  adult  males,  1375  to  1780  mm.  (54 
to  70  in.) ;  tail,  90  to  125  mm.  (3.5  to  5  in.) ;  hind  foot,  215-280  mm. 

336-897  O— 69 10 


142  NORTH  AMERICAN  FAUNA  66 

(8.5  to  11  in.).  Weight,  adult  males,  250  to  500  pounds,  rarely  600 
pounds  or  more,  normally  300  to  400  pounds.  Skull,  adult  males, 
length,  270  to  298  mm. ;  width,  158  to  185  mm.  Total  length,  adult 
females,  1270  to  1475  mm.  (50  to  58  in.) ;  tail  80  to  115  mm.  (3  to  4.5 
in.) ;  hind  foot,  190  to  240  mm.  (7.5  to  9.5  in.) .  Weight,  adult  females, 
225  to  450  pounds.  Skull,  adult  females,  length  255  to  285  mm. ;  width, 
148  to  172  mm."  (Jackson,  1961,  p.  313) . 

Habitat  and  habits. — The  black  bear  prefers  heavily  wooded  areas, 
and  is  now  confined  to  the  wildest  and  most  inaccessible  forests  of 
the  Allegheny  Mountain  section.  Individuals  may  occasionally  visit 
well-populated  agricultural  areas,  but  they  usually  do  not  remain  in 
the  neighborhood  of  humans  for  any  length  of  time. 

Except  for  females  with  cubs,  the  black  bear  is  solitary  in  habits. 
It  is  nocturnal  but  usually  does  not  wait  until  full  darkness  to  ven- 
ture forth ;  occasionally  an  individual  may  be  seen  abroad  in  the  day- 
time. These  bears  remain  dormant  from  about  the  end  of  November 
or  early  December  until  March  or  April,  usually  in  a  cavity  dug  under 
an  overturned  tree,  most  often  at  the  roots.  Sometimes  other  sites  are 
chosen,  such  as  a  cave  in  rocks,  a  hollow  tree,  or  dense  thickets. 

The  female  gives  birth  in  January  or  February ;  the  gestation  period 
is  about  225  days.  One  to  five  young  may  comprise  a  litter,  but  the 
usual  number  is  two.  Black  bears  normally  breed  only  every  other 
year. 

The  black  bear  is  an  omnivorous  animal,  consuming  a  wide  variety 
of  foods.  It  is  especially  fond  of  fruits  and  eats  large  quantities  of 
blueberries,  blackberries,  strawberries,  and  raspberries.  It  also  con- 
sumes quantities  of  mice,  insects,  and  fish  and  occasionally  wiU  kill 
and  devour  sheep  and  pigs.  In  the  autumn,  when  nuts  are  available,  it 
feeds  extensively  on  acorns  and  beechnuts.  In  addition,  it  will  occa- 
sionally eat  grass,  roots,  and  fungi. 

Remarks. — Mansueti  (1950,  pp.  14-16)  has  thoroughly  investigated 
the  former  and  present  distribution  of  this  species  in  Maryland. 
According  to  him,  the  black  bear  was  at  one  time  distributed  through- 
out the  State  and  was  plentiful.  Early  settlers  considered  it  the  banc^ 
of  their  existence.  Today  the  black  bear  still  exists  in  restricted  por- 
tions of  the  western  part  of  the  State,  but  in  the  past  2  or  3  decades 
it  has  been  on  the  verge  of  extinction.  A  1937  report  by  the  U.S. 
Bureau  of  Biological  Survey  (Big-Game  Inventory  of  the  United 
States,  1937,  Wildlife  Research  and  Management  Leaflet  BS-122, 
January  1939)  placed  the  total  number  of  bears  in  Maryland  at  150. 
Tlie  1938  summary  (Big-Game  Inventory  of  the  United  States,  1938, 
U.S.  Bureau  of  Biological  Survey,  Wildlife  Leaflet  BS-142,  August 
1939)  placed  the  number  at  50.  By  1946  (Big-Game  Inventory  of  the 
United  States,  1946,  U.S.  Fish  and  Wildlife  Service,  Wildlife  Leaflet 


MAMMALS  OF  MARYLAND  143 

303,  March  1948)  the  estimate  was  down  to  25;  in  1951  (Inventory  of 
Big-Game  Animals  of  the  United  States,  1950  and  1951,  U.S.  Fish 
and  Wildlife  Service,  Wildlife  Leaflet  342,  October  1952)  to  20;  and 
by  1956  to  12. 

Bears  are  still  occasionally  seen  in  Allegany  and  Garrett  Counties. 
Theodore  A.  Bookhout,  formerly  with  the  University  of  Maryland's 
Natural  Resources  Institute,  has  informed  me  of  several  recent  sight- 
ings. In  the  fall  of  1963,  one  was  seen  near  Murley's  Branch,  a  few 
miles  south  of  Flintstone,  Allegany  County ;  in  October  1963,  one  was 
seen  on  Maryland  Route  55,  approximately  2  miles  north  of  Cor- 
riganville,  Allegany  County;  on  January  3,  1964,  bear  tracks  were 
seen  on  Wagner  Road  just  north  of  Oldtown,  Allegany  County. 

As  Mansueti  (1950,  p.  16)  notes,  however,  western  Maryland  is 
becoming  more  densely  populated  and  the  extensive  forests  are  being 
laid  waste,  and  the  black  bear  will  disappear  mainly  because  it  is 
unwanted.  At  most  it  will  remain  in  only  the  most  remote  and  inac- 
cessible of  Maryland  wildlife  sanctuaries. 

Family  PROCYONIDAE  (raccoons,  coatis,  etc.) 

RACCOON 

Procyon  lotor  lotor  (Linnaeus) 

[Ursics']  Zo^or Linnaeus,  Syst.  nat., ed.  10, 1 :  48, 1758. 

Procyon  lotor  m-aritirmis  Dozier,  J.  Mammal.,  29(3)  :  286,  August 
1948.  (Type  locality :  Blackwater  National  Wildlife  Refuge,  Dor- 
chester County,  Md.) 

Type  locality. — Pennsylvania  (fixed  by  Thomas,  Proc.  Zool.  Soc.  London,  p. 
140,  March  1911). 

General  distribution. — "Nova  Scotia,  southern  New  Brunswick,  southern 
Quebec,  and  southern  Ontario,  south  through  the  eastern  United  States  to  North 
Carolina  from  the  Atlantic  coast  west  to  Lake  Michigan,  Indiana,  southern  Illi- 
nois, western  Kentucky  and  probably  eastern  Tennessee."  (Goldman,  1950,  p.  33.) 

Distribution  in  Maryland. — Common  in  all  sections  of  the  State, 
but  particularly  abundant  in  the  Eastern  Shore  section. 

Distinguishing  characteristics. — Teeth  3/3,  1/1,  4/4,  2/2,  =  40; 
size  medium;  form  robust;  fur  long  and  coarse;  coloration  of  upper 
parts  grizzled  gray,  brownish,  and  blackish,  there  being  considerable 
individual  variation;  sides  paler  than  upper  parts;  under  parts  dull 
grayish  brown,  tinged  with  yellowish  gray  or  white;  black  band,  or 
mask,  extends  through  eyes  and  across  cheeks;  remainder  of  face 
yellowish  gray;  tail  alternately  banded  brownish  gray  or  blackish 
and  yellow,  with  five  to  seven  dark  rings,  always  terminating  in  a 
dark  band. 


144 


NORTH  AMERICAN  FAUNA  66 


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Vvocyon  lotor  lotor 
#     Specimens   examined 

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FiGUKE  47. — Distribution  of  Procyon  lotor  lotor. 


The  racoon  is  easily  distinguished  from  all  other  Maryland  mam- 
mals by  the  dark  facial  mask  and  the  long-haired  tail  ringed  with 
black  and  yellow. 

Measurements. — External  and  cranial  measurements  of  four  adult 
females  from  the  Blackwater  National  Wildlife  Refuge,  Dorchester 
County,  are:  Total  length  749.5  (718-762) ;  tail  236.7  (210-254) ;  hind 
foot  108  (102-114)  ;  condylobasal  length  of  skull  110.9  (107.1-114.2) ; 
zygomatic  breadth  67.1  (62.7-69.7)  ;  postorbital  breadth  23.3  (22.5- 
23.8)  ;  length  of  maxillary  toothrow  41.3  (39.9-43.8)  ;  breadth  of  ros- 
trmn  at  incisors  23.7  (23.1-24.2).  External  measurements  of  three  and 
cranial  measurements  of  four  adult  males  are :  Total  length  736,  736, 
762;  tail  229,  229,  254;  hind  foot  102, 102,  102;  condylosabal  length  of 
skull  114.1  (110.9-117.9) ;  zygomatic  breadth  67.4  (64.9-69.9)  ;  post- 
orbital  breadth  22.5  (21.0-24.7)  ;  upper  maxillary  toothrow  26.1  (25.3- 
26.5). 

Three  adult  males  and  three  adult  females  from  Laurel,  Prince 
Georges  County,  measure  cranially:  Condylobasal  length  109.6,  112.7, 
111.7,  106.3,  104.4,  108.8 ;  zygomatic  breadth  67.4,  67.8,  74.9,  67.7,  68.4, 
65.1;  postpalatal  breadth  24.2,  22.1,  23.5,  22.1,  22.4,  23.2;  length  of 
maxillary  toothrow  40.9,  41.6,  41.1,  40.7,  39.0,  40.1 ;  breadth  of  rostrum 
at  incisors  25.6, 25.1, 26.1, 23.5, 22.5, 22.8. 

Habitat  and  habits. — The  raccoon  is  cosmopolitan  in  habitat  pref- 
erence, being  found  in  woods,  swamps,  and  marshes,  including  salt- 


MAMMALS  OF  MABYLANID  145 

water  marshes  of  the  Atlantic  barrier  beaches.  Uhler  and  Llewellyn 
(1952,  p.  83)  report  that  at  the  Patuxent  Research  Center,  near  Laurel, 
Prince  Georges  County,  the  outstanding  habitat  type  was  bottomland 
forest,  followed  by  cultivated  fields  (mainly  those  with  com),  hedge 
rows  and  wood  margins,  particularly  if  leading  to  cornfields.  Rac- 
coons were  also  abundant  around  marshy  lake  borders  and  in  swamps. 

The  raccoon  is  a  very  adept  climber.  Although  it  usually  makes 
its  home  in  a  hollow  tree,  it  sometimes  will  utilize  a  fissure  in  a  cliff, 
or  a  hole  among  rocks.  Raccoons  rapidly  diminish  in  numbers  when 
trees  are  cut  over,  and  will  either  die  off  or  leave  the  area  after  all 
the  trees  are  gone. 

The  raccoon  is  nocturnal,  and  forages  for  its  food  after  sunset.  Its 
diet  consists  of  fish,  crayfish,  frogs,  and  mussels,  as  well  as  poultry, 
mice,  birds,  eggs,  reptiles,  and  insects.  In  season,  it  eats  considerable 
amounts  of  vegetable  matter  such  as  nuts,  fruits,  berries,  and  corn. 

In  more  northern  climates  the  raccoon  hibernates,  but  in  Maryland 
it  remains  active  the  year  round  except  in  the  coldest  portions  of  the 
western  part  of  the  State.  The  species  breeds  in  January  and  Febru- 
ary, and  some  63  days  later  females  give  birth  to  two  to  six  young. 
The  cubs  are  born  blind  and  remain  so  for  about  19  days ;  they  suckle 
for  2  months,  and  remain  in  the  family  circle  through  the  winter. 

Remarks. — Maryland  raccoons  differ  in  no  significant  way  from 
Pennsylvania  and  New  York  specimens.  Dozier  (1948a,  p.  286)  sep- 
arated the  raccoons  inhabiting  the  marshes  of  the  Delmarva  Peninsula 
from  those  living  in  the  surrounding  woods  as  a  distinct  subspecies, 
Procyon  lotor  rnaritiTnus.  I  have  examined  the  type  of  this  race,  as 
well  as  the  series  designated  by  Dozier  as  representing  it,  and  am 
unable  to  separate  it  from  raccoons  inhabiting  other  parts  of  Mary- 
land. All  the  diagnostic  characters  mentioned  by  Dozier  (paler  colora- 
tion ;  longer  but  more  sparse  guard  hairs ;  much  smaller  size ;  shorter, 
more  pointed  and  less  prominently  banded  tail;  relatively  shorter 
caudal  vertebrae;  smaller  and  more  distinctly  curved  baculum;  and 
various  cranial  characters)  are  either  within  the  limits  of  individual 
variation  of  P.  I.  lotor.,  or  are  so  slightly  marked  that  I  have  been 
unable  to  distinguish  them.  Consequently,  I  consider  Procyon  lotor 
maritimus  Dozier  to  be  a  synonym  of  Procyon  lotor  lotor  (Linnaeus) . 

Specimens  examined. — Anne  Arundel  County :  Rutland,  1.  Calvert 
County:  Prince  Frederick,  1;  St.  Leonard  (near),  1;  Sollers,  9. 
Charles  County:  Marshall  Hall,  1;  Newport,  1.  Dorchester  County: 
Blackwater  National  Wildlife  Refuge,  69 ;  Cambridge,  1 ;  Castlehaven 
Point,  3;  Crapo,  1;  Crocheron,  1;  Golden  Hill,  2;  House  Point,  11; 
Kirwan's  Neck,  2;  Meekins  Neck,  1 ;  Punch  Island,  6;  Robbins  (near), 
1 ;  Shorters  Wharf,  1 ;  Vienna,  1 ;  Worlds  End  Creek,  1.  Frederick 


146  NORTH  AMERICAN  FAUNA  66 

County:  Jefferson,  2.  Kent  County:  Chestertown,  2;  Millington  (4 
miles  NE),  1.  Montgomery  County:  Cabin  John,  1.  Prince  Georges 
County:  Bowie,  1;  Brancliville,  1;  Laurel,  39;  Patuxent  Research 
Center,  4.  Somerset  County:  Cokesbury,  4;  Mariimsco,  3;  Rehoboth 
(near),  2;  Westover,  2;  Whitehaven  (across  Wicomico  River  from), 
3.  Talbot  County:  St.  Michaels,  1.  Wicomico  County :  Bivalve  (near), 
1 ;  Whitehaven,  1.  Worcester  County :  Assateague  Island,  1 ;  Pocomoke 
City  (vicinity) ,  17.  District  of  Coluiribia:  1. 

Other  records  and  reports. — Baltimore  County:  Bare  Hills-Lake 
Roland  area  (Bures,  1948,  p.  66) ;  Loch  Raven  (Kolb,  1938) ;  Pa- 
tapsco  State  Park  (Hampe,  1939,  p.  5).  Garrett  County:  Blooming 
Rose  (Browing,  1928,  p.  26) ;  Cranesville  Pine  Swamp  (Mansueti, 
1958,  p.  83).  Montgomery  County :  Burtonsville  (Herman  et  al.,  1957, 
p.  113-114) ;  Plmnmers  Island  (Goldman  and  Jackson,  1939,  p.  132). 
Wicomico  County :  Salisbury,  a  few  miles  east  (Kilham  and  Herman 
1955,  p. 499). 

Family  MUSTELIDAE  (weasels,  skunks,  otters,  etc.) 

ERMINE 
Mustela  erminea  cicognanii  Bonaparte 

Mustela  cigognanii  [szc]  Bonaparte,  Charlesworth's  Mag.  Nat.  Hist., 
2 :  37, 1838. 

Type  locality. — Eastern  United  States. 

General  distribution. — Southeastern  Ontario,  southern  Quebec,  and  Maine, 
south  through  extreme  northeastern  Ohio  and  Pennsylvania  into  Maryland. 

Distribution  in  Maryland. — Probably  very  rare  in  the  Allegheny 
Mountain,  Ridge  and  Valley,  and  Piedmont  sections,  and  absent  from 
the  Western  Shore  and  Eastern  Shore  sections.  The  species  is  most 
numerous  in  the  coniferous  forests  of  the  northern  portion  of  its  range, 
but  even  in  the  north  it  is  uncommon  in  coastal  regions  and  con- 
sequently it  probably  does  not  occur  in  Maryland's  coastal  plain.  It 
has  been  reported  from  the  State  only  once. 

Distinguishing  characteristics. — Teeth  3/3,  1/1,  3/3,  1/2,  =  34; 
size  medium;  body  long  and  slender;  legs  short;  tail  moderately  short, 
averaging  about  35  percent  of  head  and  body  length,  well  haired  and 
slightly  bushy,  tipped  with  black  above  and  below;  coloration  of  upper 
parts  in  summer  dark  brown  extending  to  the  outer  parts  of  the  legs 
and  feet;  color  of  underparts  whitish,  usually  tinged  with  yellow; 
winter  coloration  white  except  for  tip  of  tail  which  remains  black. 

This  species  resembles  the  long-tailed  weasel  {Mustela  frenata)  in 
general  appearance  and  in  coloration,  but  is  considerably  smaller,  and 
shorter  tailed.  Wlien  using  size  as  a  criterion  in  separating  the  two 
species,  it  is  necessary  to  take  into  account  the  sex  of  the  individual. 


MAMMALS  OF  MARYLAND 


147 


Mustela  erminea  cicognami 
9  Specimens  examined 


Figure  48. — Distribution  of  Mustela  erminea  cicognanii. 


Male  and  female  long-tailed  weasels  are  larger  than  male  and  female 
ermines,  but  since  the  males  in  both  species  are  larger  than  the  fe- 
males, a  large  male  ermine  may  approach  in  size  a  small  female  long- 
tailed  weasel. 

Measurements. — Hall  (1951,  p.  119)  gives  the  averages  and  extremes 
of  external  measurements  of  seven  adult  and  subadult  males  from 
New  York  and  Pennsylvania  as  follows:  Total  length  266  (240-295)  ; 
length  of  tail  74  (66-80)  ;  length  of  hind  foot  36  (33-39).  He  gives 
the  external  measurements  of  12  adult  and  subadult  females  from 
Maine  and  the  area  south  to  central  Pennsylvania  as:  Total  length 
243  (225-260)  ;  length  of  tail  63  (55-72) ;  length  of  hind  foot  29.8 
(26-32). 

Some  cranial  measurements  given  by  Hall  (1951,  pp.  434-435)  of 
nine  adult  and  subadult  males  from  New  York  and  Pennsylvania  are : 
Basilar  length  (of  Hensel)  35.7  (33.8-37.6) ;  zygomatic  breadth  20.3 
(19.0-20.6)  ;  interorbital  breadth  8.6  (7.7-8.9)  ;  mastoidal  breadth 
18.2  (17.3-18.8) .  Four  adult  and  subadult  females  from  New  York  and 
Pennsylvania  measure  eranially:    Basilar  length    (of  Hensel)    32.4 

(31.4-33.3);  zygomatic  breadth  ,  ,  17.5,  18.0;   interorbital 

breadth  7.5  (7.2-7.8)  ;  mastoidal  breadth  15.7  (average  of  3,  15.3- 
16.0). 


148  NORTH  AMERICAN  FAUNA  66 

Vasquez  (1956,  p.  114),  who  collected  the  only  Maryland  record  of 
this  species,  says  that  no  external  measurements  are  available  for  the 
specimen,  but  he  does  give  the  following  cranial  measurements  for  the 
female:  Condylobasal  length  38.1;  basilar  length  (of  Hensel)  34.3; 
mastoidal  breadth  17.1 ;  depth  of  skull  at  first  molars  9.1. 

Habitat  and  habits. — ^This  animal  is  most  abundant  in  the  northern 
United  States  and  Canada  where  it  inhabits  the  deep  spruce  stands. 
In  the  southern  part  of  its  range  it  is  often  encountered  in  brushy  fields 
and  hedgegrows,  and  it  is  particularly  fond  of  stone  walls,  where  it 
can  elude  its  enemies  and  catch  the  small  mammals  and  birds  which 
form  its  prey. 

This  weasel  generally  does  not  make  its  own  home,  but  prefers  to 
occupy  the  chambers  of  some  other  mammal,  most  often  a  chipmunk's 
cavity  beneath  a  stump  or  pile  of  rocks.  Its  nest  is  composed  of  fur  and 
feathers  from  the  animals  on  which  it  feeds. 

According  to  Hamilton  (1943,  p.  136)  all  the  evidence  suggests 
that  these  weasels  mate  in  the  early  summer,  and  the  fertilized  eggs, 
after  undergoing  a  short  development  remain  quiescent  for  several 
months.  Embryonic  development  continues  in  the  late  winter,  and  the 
four  to  nine  young  are  born  usually  in  mid-April.  Hamilton  states 
that  the  male  weasel  assists  in  bringing  food  to  the  young  during  their 
infancy  and  that  there  is  much  evidence  that  weasels  remain  paired 
throughout  the  year. 

Hamilton  (1933b,  p.  333)  reports  fall  and  winter  food  of  191  ermine 
in  New  York  State  as  composed  of  the  following :  Meadow  mice  35.7 
percent;  undetermined  mammals  (principally  mice)  16.3  percent; 
short-tailed  shrews  15.1  percent;  white-footed  mice  11.4  percent;  rab- 
bits 9.0  percent ;  long-tailed  shrews  4.9  percent ;  rats  4.4  percent ;  and 
chipmunks  3.6  percent.  In  addition,  birds  comprised  some  2.1  percent, 
and  reptiles  and  amphibians  1.2  percent  of  the  fall  and  winter  food 
of  weasels  (354  Mustela  enninea  and  Mustela  frenata) . 

Remarks. — This  species  has  been  recorded  only  once  from  Maryland. 
Vazquez  (1956,  pp.  113-114)  reports  that  a  cat  killed  an  ermine  on  the 
heavily  wooded  grounds  of  the  Honeywell  School,  4  miles  northwest 
of  Bethesda,  Montgomery  County,  on  27  May  1954.  Prior  to  this, 
Maryland  was  considered  far  south  of  the  normal  range  of  the  ermine, 
and  it  is  possible  that  the  animal  escaped  from  captivity.  Vazquez 
states  that  the  coloration  is  peculiarly  grayish,  and  that  its  cranial 
measurements  are  slightly  larger  than  those  of  female  Mustela  erminea 
clcognanii  and  approach  those  of  males  of  this  race.  The  skin  and  skull 
of  the  specimen  are  in  Vazquez'  private  collection  and  I  have  not  ex- 
amined them. 


MAMMALS  OF  MARYLAND 


149 


LONG-TAILED  WEASEL 
Mustela  frenata  noveboracensis  (Emmons) 

Putorius  NovehoraceTisis  Emmons,  a  report  on  the  quadrupeds  of 


Massachusetts, 


p.  45, 1840. 


Type  locality. — Williamstown,  Berkshire  County,  Mass. 

General  distribution. — From  Wisconsin  east  through  Michigan,  southwestern 
Ontario,  southern  Quebec,  and  southeastern  Maine,  south  through  the  eastern 
United  States  to  North  Carolina,  western  South  Carolina,  northern  Georgia, 
and  Alabama,  west  to  the  Mississippi  and  St.  Croix  Rivers. 

Distribution  in  Maryland. — Occurs  in  all  sections  of  the  State. 

Distinguishing  characteristics. — A  large  weasel,  similar  in  colora- 
tion and  general  appearance  to  the  ermine,  but  larger  and  with  a  longer 
tail.  It  is  generally  believed  that  except  in  the  coldest  portions  of  the 
Allegheny  Mountain  section,  most  Maryland  long-tailed  weasels  re- 
main in  brown  pelage  the  year  round,  and  the  majority  of  winter- 
killed specimens  from  Maryland  that  I  have  examined  are  in  brown 
pelage.  There  is,  however,  one  male  from  Gaithersburg,  Montgomery 
County,  and  another  from  Patuxent,  Prince  Georges  County,  in  the 
National  collections  that  are  entirely  white  except  for  the  customary 
black  tail  tip. 

Male  long-tailed  weasels  are  strikingly  larger  than  females.  So 
pronounced  is  this  secondary  sexual  trait  that  some  early  writers 


1 1 

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Mustela  frenata  noveboracensis 
•    Specimens   examined                             J. 
O    Specimens   reported 

73-                                                            76' 

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BOM 

Figure  49. — Distribution  of  Mustela  frenata  noveboracensis. 


160  NORTH  AMERICAN  FAUNA  66 

thought  the  two  sexes  must  represent  distinct  species.  Since  the  female 
long-tailed  weasel  is  so  small,  it  is  possible  to  mistake  her  for  an  er- 
mine, and  due  allowance  must  be  made  for  sex  when  separating  these 
species  on  the  basis  of  size. 

MeasureTnents. — External  measurements  of  12  adult  males  from 
various  parts  of  Maryland  are:  Total  length  382  (340^29)  ;  tail  131.6 
(110-155) ;  hind  foot  48  (34-^8),  Seven  females  from  various  parts 
of  the  State  have  the  following  external  measurements.  Total  length 
286.6  (253-315)  ;  tail  93.1  (80-122)  ;  hind  foot  34  (32-38). 

Cranial  measurements  of  10  adult  males  from  Laurel,  Prince 
Georges  County,  are:  Basilar  length  42.7  (40.8-44.3);  zygomatic 
breadth  25.6  (23.5-27.3) ;  interorbital  breadth  9.8  (9.0-10.8)  ;  mas- 
toidal breadth  22.4  (21.^24.0).  Cranial  measurements  of  three  adult 
females  from  Laurel  are:  Basilar  length  36.1,  36.4,  36.5;  zygomatic 

breadth  21.5,  21.7, ;  interorbital  breadth  7.9,  9.1,  9.1;  mastoidal 

breadth  18.9, 19.0, 18.2. 

Habitat  and  habits. — This  weasel  prefers  bushy  field  borders,  brush- 
land,  open  woodland,  and  woodland  bordering  cultivated  fields  and 
pastures.  It  is  quite  adaptable  and  willing  to  live  in  close  proximity  to 
man  as  long  as  suitable  prey  is  available.  Recently,  I  found  one  dead  on 
a  road  in  the  middle  of  Kensington,  Montgomery  County,  where  the 
only  suitable  habitat  for  some  distance  was  the  bushy  area  bordering  a 
railroad  track  that  runs  through  the  center  of  town.  Uhler  and  Llewel- 
lyn (1952,  p.  81)  report  that  during  a  study  made  at  the  Patuxent 
Research  Center  in  Prince  Georges  County,  only  four  weasels  were 
taken  in  three  trapping  seasons.  Of  these,  two  were  taken  along  hedge- 
rows, one  in  upland  forest,  and  one  along  the  Patuxent  River.  In  the 
Bare  Hills-Lake  Roland  area,  Bures  (1948,  p.  66)  thought  these  weasels 
were  quite  rare  at  first.  Subsequent  investigation  revealed,  however, 
that  they  were  more  common  than  he  suspected,  and  that  they  range 
throughout  the  area  except  for  the  marsh  and  Serpentine.  He  says  that 
they  seem  to  use  the  railroad  right-of-way  as  a  natural  highway  regu- 
larly; their  mortality  rate  was  high  there,  since  an  average  of  four 
s,pecimens  a  year  were  recorded  killed  by  passing  trains.  In  an  area  as 
small  as  that  in  which  Bures  was  working,  this  is  a  high  number  of 
weasels. 

This  species  generally  does  not  make  its  own  burrow,  but  uses  an 
abandoned  one  of  a  chipmunk  or  mole.  Sometimes  it  will  utilize  a  hole 
among  rocks  or  under  a  stump.  The  nest  center  is  usually  filled  with 
grass  and  lined  with  fur  and  feathers  from  the  weasel's  prey. 

Mating  in  this  species  occurs  in  July  and  August.  The  gestation 
period  is  very  prolonged,  averaging  about  279  days,  but  as  in  the 
ermine,  the  embryo  remains  quiescent  throughout  most  of  this  period 
and  only  begins  to  develop  rapidly  during  the  last  27  days.  The  young. 


MAMMALS  OF  MARYLAND  181 

numbering  between  six  and  eight,  are  born  from  mid- April  to  mid- 
May.  Hamilton  (1933b,  p.  328)  states  that  the  male  stays  with  the 
female  and  assists  in  caring  for  the  young.  He  says  that  he  has  several 
times  seen  a  male  of  this  species  carrying  food  to  a  den  of  young  ones. 

Like  the  ermine,  the  long-tailed  weasel  is  strictly  carnivorous  in  diet. 
Hamilton  (1933b,  p.  333)  lists  the  percentages  of  fall  and  winter  food 
of  this  species  in  New  York  State  as  follows:  Meadow  mice  33.6; 
cottontail  rabbits  17.3;  white  footed  mice  11.3;  rats  9.1;  short-tailed 
shrews  5.9;  squirrels  2.7;  chipmunks  1.0;  star-nosed  moles  0.8;  musk- 
rat  0.8.  In  addition  to  this,  a  small  percentage  of  birds  and  reptiles  is 
consumed. 

SpeclTnens  examined. — Allegany  County :  Piney  Mountain,  2  (Coll. 
U.  Md.).  Anne  Arundel  County:  Patuxent  (2  miles  S),  1.  Howard 
County :  Hanover.,  1 ;  Long  Corner,  1.  Montgornery  County:  Bethesda, 
1;  Chevy  Chase,  1;  Foxhall  Village  (D.C.?  not  located  in  Maryland), 
1 ;  Gaithersburg,  1 ;  Garrett  Park,  1 ;  Kensington,  1 ;  Linden,  1 ;  Olney, 
1 ;  Plummers  Island,  3.  Prince  Georges  County :  Andrews  Air  Force 
Base  (near),  1;  Bladensburg,  1;  Branchville,  1;  Laurel,  17;  Oxen 
Hill,  1.  Talhot  County :  Easton,  1.  District  of  Colunnbia:  8. 

Other  records  and  reports. — Baltiirvore  County:  Bare  Hills-Lake 
Roland  area  (Bures,  1948,  p.  66)  ;  Halethorpe  (Hampe,  1943,  p.  66)  ; 
Loch  Raven  (Seibert,  1939,  p.  21) ;  Patapsco  State  Park  (Hampe, 
1938,  p.  6).  Calvert  County:  Plum  Point  (identified  from  photograph 
submitted  by  John  F.  Fales).  Dorchester  County:  Cambridge  (five 
specimens  in  collection  of  R.  W.  Jackson,  examined  by  Hall,  1951,  p. 
228).  Garrett  Comity :  Grantsville  (E  A.  Preble,  in  field  notes,  men- 
tions seeing  one,  June  1899).  Montgomery  County:  Sandy  Spring 
(Bailey,  1923,  p.  126). 

(LEAST  WEASEL) 
Mustela  nivalis  allegheniensis  (Rhoads) 

Putorius  allegheniensis  Rhoads,  Proc.  Acad.  Nat.  Sci.  Philadelphia, 
52:  751, 25  March  1901. 

Type  locality. — ^Near  Beallsville,  Washington  County,  Pa. 

General  distribution. — From  Wisconsin  and  northern  Illinois  eastward  through 
northern  Indiana,  Michigan,  and  Ohio  into  southwestern  New  York  and  Pennsyl- 
vania, thence  southward  in  the  Appalachians  to  North  Carolina. 

Distribution  in  Maryland. — This  species  has  not  been  recorded  as 
yet  from  Maryland,  but  it  has  been  taken  in  nearby  Pennsylvania, 
West  Virginia,  and  Virginia,  and  probably  ranges  through  the  Al- 
legheny Mountain  section  of  Maryland  and  possibly  in  the  Ridge 
and  Valley  section  as  well. 

Distingmshing  characteristics. — A  very  small  weasel,  similar  to 
both  M.  frenata  and  M.  ermin^n  in  coloration  and  general  form,  but 


152  NORTH  AMERICAN  FAUNA  66 

considerably  smaller  than  either.  It  may  readily  be  distinguished  from 
both  these  species  by  its  very  short  tail  and  the  complete  lack  of  a 
black  tail  tip. 

Measurements. — "Male :  An  adult  or  subadult  from  Fair  Oaks,  Pa., 
a  subadult  from  Finleyville,  Pa.,  and  an  adult  from  Huttonsville, 
W.  Va.,  measure  respectively  as  follows:  Total  length,  206,  194,  191 
(average  197)  ;  length  of  tail,  37,  32, 28  (32)  ;  length  of  hind  foot,  23  in 
each. 

"Female:  Two  young  from  Leasuresville,  Pa.,  and  Middle  Paxton 
Twp.,  Pa.,  measure  respectively,  as  follows:  total  length,  188,  172; 
length  of  tail,  33,  30;  length  of  hind  foot,  20.5,  21."  (Hall,  1951,  p. 
187-188.) 

Some  of  the  cranial  measurements  listed  by  Hall  (1951,  p.  440^41) 
of  an  adult  male  from  Huttonsville,  W.  Va.,  and  an  adult  female  from 
Beallsville,  Pa.,  are  Basilar  length  (of  Hensel)  28.5,  28.0,  zygomatic 
breadth  16.7, 14.6 ;  interorbital  breadth  7.1,  6.2 ;  mastoidal  breadth  15.1, 
13.5. 

Habitat  and  habits. — This  species  inhabits  both  the  deep  forests 
and  the  fields  and  pastures  within  its  range.  It  is  a  rare  mammal  how- 
ever, and  is  seldom  encountered. 

Little  is  known  of  its  habits.  Hamilton  (1943,  p.  139)  says  that  nests 
have  been  found  beneath  corn  shocks,  in  shallow  burrows  bordering 
streams,  and  in  similar  places.  The  few  nests  that  have  been  dis- 
covered were  composed  of  grasses  and  mouse  fur.  Hamilton  states  that 
the  breeding  habits  of  this  species  apparently  differ  from  those  of  its 
larger  relatives.  He  says  that  young  with  unopened  eyes  have  been 
discovered  in  midwinter,  while  nest  young  and  lactating  females  have 
been  found  in  Pennsylvania  during  October,  January,  and  February. 
These  litters  numbered  from  three  to  six  young.  The  female  parent  was 
always  in  attendance.  From  this  he  says  that  the  young  are  probably 
bom  at  various  seasons  and  there  is  a  likelihood  of  more  than  one  litter 
a  year. 

Hall  (1951,  p.  177)  says  that  food  of  the  least  weasel  consists  of 
harvest  mice,  deer  mice,  meadow  mice,  red-backed  mice,  and  possibly 
insects. 

MINK 
Mustela  vison  mink  Peale  and  Palisot  de  Beauvois 

Mustela  mink  Peale  and  Palisot  de  Beauvois.  A  scientific  and  descrip- 
tive catalogue  of  Peal's  museum,  Philadelphia,  p.  39,  1796. 

Type  locality. — Maryland. 

General  (listrlbution. — Eastern  United  States  from  southeastern  Maine,  south 
to  coastal  North  Carolina,  and  inland  (excepting  the  higher  elevations  of  the 
Appalachians)  through  Pennsylvania,  Michigan,  Georgia,  and  Alabama  to 
Missouri. 


MAMMALS  OF  MARYLAND  153 


Mustela  vison 
0  Specimens  examined 
O  Specimens  reported 


Figure  50. — Distribution  of  Mustela  vison. 

Distribution  in  Maryland. — The  species  is  Statewide  in  distribution ; 
the  subspecies  mink  occurs  throughout  most  of  Maryland,  but  may  be 
replaced  by  the  race  vison  at  higher  elevations  in  the  Allegheny  Moun- 
tain section.  This  very  dark  northern  race,  vison.,  has  been  reported  in 
the  Appalachians  to  the  south  of  Maryland  (Kellogg,  1939,  p.  262), 
but  the  only  specimen  available  from  the  Allegheny  Mountain  section 
of  Maryland  is  a  zoo  animal  and  its  subspecific  affinities  are  indeter- 
minable. 

Distinguishing  characteristics. — A  very  large  weasel,  with  a  fairly 
long,  bushy  tail ;  coloration  dark  glossy  brown  over  entire  body,  except 
for  a  whitish  chin  spot  and  an  occasional  white  streak  on  the  neck  or 
white  spot  on  the  chest  or  belly ;  pelage  thick  and  dense,  adapted  for  an 
aquatic  life. 

The  mink  may  distinguished  from  the  long-tailed  weasel  by  its 
larger  size,  and  absence  of  a  white  belly.  It  is  similar  to  an  otter  in 
coloration,  but  is  smaller  and  does  not  have  a  broad-based  tail. 

Measurements. — Males  considerably  larger  than  females.  A  typical 
adult  male  and  female  from  Montgomery  County  have  the  following 
external  and  cranial  measurements:  Total  length  650,  547;  tail  225, 
193,  hind  foot  70,  54;  basilar  length  62.4,  56.0;  zygomatic  breadth  42.1, 
36.3;  interorbital  breadth  12.9,  13.7;  mastoidal  breadth  34.4,  30.5. 

Habitat  and  habits. — The  mink  always  lives  near  water.  It  is  found 
around  lakes,  in  or  near  marshes,  and  along  the  banks  of  rivers  or 


15*  NORTH  AMERICAN  FAUNA  66 

streams.  It  prefers  forested,  log-strewn,  and  bushy  areas.  At  the 
Patuxent  Wildlife  Eesearch  Center  near  Laurel,  Prince  Georges 
County,  Uhler  and  Llewellyn  (1952,  p.  84)  found  them  along  lake 
margins,  by  a  small  stream,  and  along  the  Patuxent  River.  Bailey 
(1923,  p.  125)  reported  that  in  the  early  1920's  they  were  fairly  com- 
mon along  the  banks  of  almost  any  stream  in  Washington,  D.C.,  and 
that  they  followed  Rock  Creek  well  down  into  the  city.  Today,  owing 
to  stream  pollution  and  other  factors  few,  if  any,  mink  occur  along 
Rock  Creek  in  Washington. 

Mink  make  their  home  under  large  trees  which  line  banks  of  streams 
along  which  they  live.  They  also  inhabit  muskrat  lodges  or  natural 
cavities  along  the  banks  of  streams,  rivers,  lakes,  or  marshes.  Males 
and  females  build  separate  nests,  but  females  build  more  elaborate 
ones,  lining  them  with  grass,  feathers,  and  fur  to  make  a  snug  home 
for  the  young. 

The  breeding  season  for  mink  begins  in  January  and  extends 
through  March ;  the  gestation  period  is  variable,  from  39  to  76  days, 
depending  on  when  mating  has  occurred;  the  later  the  mating,  the 
shorter  the  gestation  period.  Three  to  six  young  are  born  in  April  or 
May,  but  as  many  as  10  have  been  reported. 

Mink  range  over  a  wide  area  to  procure  their  food,  which  consists 
of  any  reptiles,  amphibians,  small  mammals,  and  birds  obtainable.  In 
areas  where  muskrat  abound,  such  as  the  muskrat  marshes  of  the 
Delmarva  Peninsula,  mink  may  feed  extensively  on  them.  Llewellyn 
and  Uhler  (1952,  p.  199),  in  studies  conducted  at  the  Patuxent  Re- 
search Center,  report  that  it  is  usually  difficult  to  get  food-habits 
material  from  trapped  mink  since  their  digestion  is  so  rapid.  They 
state  that  frequently  stomachs  of  the  animals  studied  were  empty,  and 
only  digested  blood  was  found  in  the  intestines.  They  were  only  able 
to  obtain  six  stomachs  and  four  scats  suitable  for  tabulation.  In  none 
of  these  was  there  any  plant  food  except  for  a  few  poison-ivy  seeds 
which  were  found  in  a  stomach  that,  contained  flicker  remains.  Pre- 
sumably the  bird  had  eaten  these  seeds  before  being  captured  by 
the  mink.  One  mink  sample  in  March  and  another  in  December  con- 
tained rabbit  hair  only.  Five  other  winter  samples  had  100  percent 
rodent  remains  consisting  of  one  meadow  mouse,  three  pine  mice,  and 
one  "wood"  mouse.  In  the  two  additional  stomachs  examined  by 
Llewellyn  and  Uhler,  one  contained  flicker  remains  and  the  other 
had  a  beetle  fragment. 

The  mink  sometimes  does  considerable  damage  to  poultry.  Bailey 
(1923,  p.  125)  says  that  he  was  told  of  a  mink  in  the  Washington  area 
that  visited  a  henhouse  and  killed  22  chickens  in  one  night  and  returned 
the  next  night  to  kill  16  more.  The  following  night,  as  the  mink  was 
returning  to  the  henhouse  again,  it  was  caught  by  a  dog. 


MAMMALS  OF  MARYLANiD  165 

Despite  the  great  number  being  bred  in  captivity,  wild-caught  mink 
are  still  in  some  demand  for  their  fur,  and  each  year  many  are  trapped 
throughout  the  country.  Maryland  does  not  rank  high  in  wild  mink 
production.  In  1966,  only  303  mink  were  reported  trapped  in  the  State 
(U.S.  Fish  and  Wildlife  Service,  Fur  Catch  in  the  United  States,  1966, 
Wildlife  Leaflet  478).  The  high  point  in  mink  trapping  in  Maryland 
over  the  past  decade  was  reached  during  the  1950-51  season  when 
4,370  animals  were  taken  (U.S.  Fish  and  Wildlife  Service,  Fur 
Catch  in  the  United  States,  1949-54,  Wildlife  Leaflet  367)  for  their 
pelage. 

Specimens  examined. — Anne  Arundel  County:  Little  Patuxent 
River,  1.  Dorchester  County:  Bloodsworth  Island,  1.  Garrett  County: 
Oakland  (through  National  Zoological  Park) ,  1.  Montgomery  County : 
Bethesda,  1 ;  Cabin  John,  2 ;  Forest  Glen,  2 ;  Garrett  Park,  1 ;  Potomac, 
1;  Sligo  Creek  (near  Takoma  Park),  1;  no  exact  locality,  2.  Prince 
Georges  County:  Bladensburg,  1;  Branchville,  2;  College  Park,  1; 
Lanham,  1 ;  Laurel,  44 ;  no  exact  locality,  1. 

Other  records  and  reports. — Montgomery  County:  Plummers  Is- 
land (Goldman  and  Jaxjkson,  1939 :  132) .  Prince  Georges  County:  Col- 
lege Station,  8  miles  NE  of  Washington;  Patuxent  Research  Center. 
(Uhler  and  Llewellyn,  1952,  p.  84) . 

STRIPED  SKUNK 

Mephitis  mephitis  nigra  (Peale  and  Pallsot  de  Beauvois) 

Viverra  nigra  Peale  and  Palisot  de  Beauvois,  A  scientific  and  descrip- 
tive catalogue  of  Peale's  museum,  Philadelphia,  p.  37,  1796. 

Type  locality. — Maryland. 

General  distribution. — New  England  and  southern  Ontario  south  to  Virginia, 
and  west  of  the  Allegheny  Mountains  from  the  lower  peninsula  of  Michigati  and 
southern  Illinois  south  to  central  Mississippi,  Alabama,  and  Georgia. 

Distribution  in  Maryland. — Distributed  throughout  the  State,  but 
most  abundant  in  the  Allegheny  Mountain,  Ridge  and  Valley,  and 
Piedmont  sections;  scarce  or  lacking  in  many  areas  of  the  Eastern 
Shore  section.  According  to  the  Service  Survey  (U.S.  Fish  and  Wild- 
life Service,  vol.  3(4),  p.  15,  December  1943),  with  the  breaking  up  of 
the  former  dense  forest  cover  the  striped  skunk  seems  to  be  slowly 
making  its  way  southward  along  the  Delmarva  Peninsula  into  Dor- 
chester County  from  Talbot  County. 

Distinguishing  characteristics. — Teeth  3/3,  1/1,  3/3,  1/2,  =  34; 
size  large;  body  heavy,  particularly  rearward;  tail  very  thick  and 
bushy;  legs  short;  pelage  dense  and  coarse;  coloration  black  with  a 
thin  white  stripe  medially  on  the  nose,  and  two  white  stripes  running 
from  head  to  tail.  The  amount  of  white  on  the  striped  skunk  is  subject 


156 


NORTH  AMERICAN  FAUNA  66 


Mephitis  mephitis  mgra 
•  Specimens  examined 
O  Specimens  reported 


FiGUBE  51. — Distribution  of  Mephitis  mephitis  nigra. 


to  considerable  individual  variation.  Some  animals  are  almost  comp- 
letely black,  while  others  are  predominately  white  on  the  back. 

This  species  cannot  be  confused  with  any  other  Maryland  mammal 
except  possibly  the  spotted  skunk  {Sjniogale)  ^  from  which  it  differs 
in  larger  size  and  in  having  two  rather  than  four  white  dorsal  stripes. 
In  Mephitis  the  nose  patch  is  always  a  slender  stripe,  whereas  in 
Spilogdls  it  is  a  broad  triangular  patch. 

Measurements. — Two  adult  males  and  two  adult  females  from  Cabin 
John,  Montgomery  County,  have  the  following  external  and  cranial 
measurements:  Total  length  597,  648,  568,  648;  tail  228,  260,  235,  270; 
hind  foot  64,  70,  57,  67;  basilar  length  of  skull  61.5,  60.5,  55.0,  60.0; 
zygomatic  breadth  43.2,  46.7,  41.4,  41.9 ;  least  interorbital  breadth  18.8, 
19.6, 19.2, 18.1 ;  maxillary  toothrow  21.3, 20.7,20.2, 20.5. 

Habitat  and  habits. — This  skunk  is  found  in  brushland,  sparse  woods 
weedy  fields  or  pastures,  under  wood  piles  and  rock  piles,  and  around 
buildings.  It  is  most  common  along  brushy  borders  of  streams  and  in 
rock  piles  and  thickets  at  the  base  of  cliffs. 

The  striped  skunk  makes  its  home  in  a  burrow  which  it  may  dig  in 
a  brushy  area  or  pasture,  or  it  may  occupy  the  burrow  of  some  other 
animal  such  as  a  woodchuck.  Occasionally  the  den  may  be  in  a  cave 
or  under  a  log  or  stump.  Burrows  average  between  18  and  20  feet  long 
and  may  reach  to  a  depth  of  3  to  4  feet  below  the  surface  of  the  ground. 


MAMMALS  OF  MARYLAND  157 

The  nest  within  the  burrow  is  a  somewhat  wider  area  lined  with  dry 
leaves  and  grass. 

The  striped  skunk  is  polygamous,  and  mating  occurs  from  Febru- 
ary until  March,  with  the  young  being  born  in  May  or  June.  Only  one 
litter  is  produced  annually,  and  between  two  and  10  (usually  six  or 
seven)  kits  comprise  a  litter.  The  gestation  period  is  60  to  62  days. 

Llewellyn  and  Uhler  (1952,  p.  200)  studied  the  food  habits  of  skunks 
at  the  Patuxent  Wildlife  Kesearch  Center,  Prince  Georges  County. 
The  results  of  their  examination  of  63  digestive  tracts  and  33  scats 
mostly  taken  in  fall  and  winter  are  summarized  as  follows: 

Plant  material  comprised  some  10  percent  of  the  food  intake.  The 
only  plant  item  found  regularly  in  the  stomach  was  persimmon,  which 
accounted  for  about  7  percent.  Also  occasionally  found  were  beechnuts, 
acorns,  corn,  wheat,  pokeberry,  blackgum,  smilax,  and  a  few  other 
fruits  and  berries ;  some  of  this  plant  material  was  apparently  garbage. 
Animal  matter  comprised  between  80  percent  and  90  percent  of  the 
food  intake;  insects  formed  almost  half  of  the  total  and  were  most 
prominent  in  the  fall.  About  20  percent  of  the  insects  consumed  con- 
sisted of  beetles,  with  scarabs  such  as  June  beetles  (mostly  larvae)  and 
Japanese  beetles  (mostly  adults)  leading  the  list.  Ground  beetles  were 
also  found  frequently.  The  next  highest  group  (11  percent)  was  made 
up  of  grasshoppers  and  crickets.  A  large  number  (5  percent)  of  true 
bugs,  chiefly  stink  bugs,  were  eaten.  In  later  summer  and  fall,  it  was 
evident  that  in  several  instances  the  skunks  had  dug  out  yellow-jacket 
nests  and  eaten  the  occupants.  Lamore  (1953,  p.  80)  reports  that  he 
found  a  striped  skunk  dead  on  the  highway  near  Beltsville,  Prince 
Georges  County,  in  August  1962.  The  animal's  stomach  was  filled  with 
yellow  jackets. 

Rodents,  chiefly  wood  mice,  meadow  mice,  and  squirrels,  comprised 
15  percent  of  the  diet;  eight  occurrences  of  rabbit  totaled  5  percent. 
Llewellyn  and  Uhler  (1952,  p.  200)  believe  that  the  squirrels  and  rab- 
bits were  probably  road  kills,  carrion,  or  hunting  cripples,  although 
remains  of  rabbits  that  could  have  been  nestlings  were  found  in  two 
scats.  Birds  were  found  in  14  stomachs  or  scats  and  made  up  7  percent 
of  the  volume.  One  box  turtle,  one  king  snake,  and  several  undeter- 
mined snakes  and  salamanders  were  also  found.  Millipedes  vere  found 
frequently  in  fall  and  winter  and  often  made  up  entire  meals.  Spiders 
also  appeared  often,  and  centipedes  occasionally,  but  their  remains 
consisted  mostly  of  legs,  so  that  their  volume  constituted  a  small  per- 
centage of  the  total. 

This  skunk,  like  its  s^wtted  relative,  possesses  a  powerful  scent  as 
a  defense  mechanism.  The  fluid  which  contains  the  scent  can  be  ejected 
for  a  considerable  distance,  and  if  it  should  strike  one's  eye  it  will 
cause  burning  and  smarting.  Burning  can  be  relieved  by  washing 

336-897  0—69 11 


158  NORTH  AMERICAN  FAUNA  66 

the  eye  in  lukewarm  water,  followed  by  flushing  with  boric  acid. 
Turpentine  is  useful  for  removing  skunk  odor  from  clothing  and 
from  skin,  and  tomato  juice  is  also  effective. 

Skunk  fur  is  commercially  valuable,  and  in  the  1965-66  trapping 
season,  161  striped  skunks  were  reported  taken  in  Maryland  by  fur 
trappers  (U.S.  Fish  and  Wildlife  Service,  Fur  Catch  in  the  United 
States,  1966,  Wildlife  Leaflet  478). 

Specvmens  examined. — Allegany  County:  Mount  Savage,  1  (Ck)ll. 
U.  Md.).  Frederick  County:  Jefferson,  1.  Montgomery  County:  Cabin 
John,  4;  Forest  Glen,  1;  Silver  Spring,  1.  Prince  Georges  County: 
Laurel,  6;  Patuxent  Research  Center,  2.  Washington  County: 
Boonesboro,l. 

Other  records  amd  reports. — Baltimore  County:  Bare  Hills-Lake 
Eoland  area  (Bures,  1948,  p.  66) ;  Loch  Raven  (Kolb,  1938) ;  Pa- 
tapsco  State  Park  (Hampe,  1939,  p.  6).  Dorchester  County:  Black- 
water  National  Wildlife  Refuge  (Service  Survey,  U.S.  Fish  and 
Wildlife  Service,  3(4),  p.  15,  December  1943).  Garrett  County: 
Cranesville  Pine  Swamp  (Mansueti,  1958,  p.  83).  Montgomery 
County:  Plummers  Island  (Goldman  and  Jackson,  1939,  p.  132). 
Prince  Georges  County:  Beltsville,  near  (Lamore,  1953,  p.  80). 

EASTERN  SPOTTED  SKUNK 
Spilogale  putorius  putorius  (Linnaeus) 

[Viverra']  putorius  Linnaeus,  Syst.  nat.,  ed.  10, 1 :  44, 1758. 

Type  ToGdlity. — ^^South  Carolina. 

General  distribution. — "Southeastern  United  States  from  Alabama,  Missis- 
sippi, and  northern  Florida  northward  through  western  and  central  GTeorgia 
and  South  Carolina  and  northward  in  the  Appalachian  Mountains  to  south- 
central  Pennsylvania."  (Van  Gelder,  1959,  p.  225). 

Distribution  in  Maryland. — Ridge  and  Valley  and  Allegheny 
Mountain  sections. 

Distinguishing  characteristics. — Teeth  3/3,  1/1,  3/3,  1/2,  =  34;  size 
small;  coloration  striking,  the  background  being  black,  striped  with 
four  white  dorsal  stripes  which  run  about  to  the  middle  of  the  back,  the 
center  ones  being  somewhat  narrower  than  the  outer ;  stripes  breaking 
up  into  patches  on  the  hind  quarters,  giving  the  skunk  a  spotted 
appearance;  broad  triangular  white  patch  on  nose  and  forehead;  small 
white  patch  in  front  of  ears;  tail  long  and  full,  broadly  tipped  with 
white. 

This  skunk  is  readily  distinguished  from  the  striped  skunk  (Mephi- 
tis mephitis)  by  the  patterning  of  its  coloration.  Spilogale  has  four 
white  stripes  on  the  body  whereas  Mephitis  has  two  (these  may  be 
highly  variable,  however,  in  length  and  breadth).  Spilogale  has  a 


MAMMALS  OF  MARYLAND 

159 

79*                                                                 76- 

1                                                                        ' 

7f>' 

\ 

7\ 

-39°-                                      SCALE 

O         lO      20       30MILES 

/ry,     i 

ji^^ 

V-                      ^r 

Spilogale  putorius  putorius 
#    Specimens   examined 
O     Specimens    reported 

Pi 

80M 

Figure  52. — Distribution  of  Spilogale  putorius  putorius. 


broad  triangular  white  nose  patch,  while  Mephitis  has  only  a  thin 
white  stripe  medially  on  the  nose.  The  spotted  skunk  is  considerably 
the  smaller  species. 

Measurements. — Van  Gelder  (1959,  p.  255)  gives  external  and  some 
cranial  measurements  of  this  subspecies  as  follows:  Males:  Total 
length  506.6  (453-610) ;  tail  180.9  (152-211) ;  hind  foot  47.8  (41-51) ; 
condylobasal  length  of  skull  57.2  (53.6-61.9) ;  zygomatic  breadth 
35.3  (32.5-37.8);  interorbital  breadth  15.5  (13.5-16.9);  length  of 
maxillary  toothrow  18.4  ( 17.0-20.5) .  Females :  Total  length  450.7  (403- 
470);  tail  171.9  (154-193);  hind  foot  44.0  (39-47);  basilar  length 
of  skull  47.6  (45.0-50.0)  ;  zygomatic  breadth  33.2  (31.8-34.8) ;  inter- 
orbital breath  15.0  (13.5-15.9)  ;  length  of  maxillary  toothrow  17.7 
(16.6-18.6). 

A  male  from  Piney  Mountain,  one-quarter  mile  north  of  U.S.  Route 
40  at  Clarysville,  Allegany  County,  has  the  following  external  and 
cranial  measurements :  Total  length  425 ;  tail  155 ;  hind  foot  45 ;  ear 
13 ;  condylobasal  length  of  skull  55.1 ;  zygomatic  breadth  34.1 ;  inter- 
orbital breadth  14.8 ;  length  of  maxillary  toothrow  17.7. 

Habitat  and  habits. — In  the  northern  part  of  its  range  this  species 
prefers  to  live  in  rock  piles  and  crevices  in  cliffs.  In  more  southern  areas 
of  the  southeastern  United  States  it  often  inhabits  wasteland  and 
cultivated  fields  and  sometimes  build  its  nest  under  farm  buildings 
or  lives  in  deserted  woodchuck  burrows.  All  of  the  areas  in  which 


100  NORTH  AMERICAN  FAUNA  66 

spotted  skunks  have  been  taken  or  observed  in  Maryland  are  similar. 
They  are  at  or  near  the  summits  of  mountains  at  altitudes  above  1,600 
feet.  They  are  characterized  by  rocky  outcrops  which  run  parallel  to 
the  summits  and  which  may  be  several  hundred  feet  in  length.  The 
vegetation  consists  of  second-growth  oaks  (Quercus  spp.)  and  hickor- 
ies {Carya  spp.),  with  black  locust  (Rohinia  pseudocacia) ,  Virginia 
pine  (Pinus  virginiana) ,  and  dense  tangles  of  wild  grape  ( Vitis  spp.) 
occasionally  present  (Bookhout,  1964,  p.  214) . 

Little  is  known  of  the  breeding  habits  of  the  spotted  skunk.  Van 
Gelder  (1959,  p.  260^270)  says  that  there  is  evidence  that  tliis  sub- 
species has  an  extended  breeding  period,  or  that  two  litters  a  year 
might  be  produced  since  there  are  records  of  females  nursing  in  both 
the  spring  and  fall.  There  are  between  two  and  six  young,  with  the 
usual  number  being  four  or  five. 

According  to  Hamilton  (1943,  p.  159)  the  food  of  this  species  during 
the  winter  months  consists  largely  of  rabbits,  mice,  and  other  small 
mammals;  during  the  summer  and  fall  it  fattens  on  fruits,  insects, 
and  birds.  Lizards,  small  snakes,  and  offal  are  not  disdained,  and 
the  spotted  skunk  will  steal  eggs  and  kill  chicks.  It  is  fond  of  persim- 
mons and  various  other  fruits  in  season. 

This  skunk  possesses  a  means  of  defense  consisting  of  a  characteristic 
evil-smelling  fluid  which  is  secreted  by  two  anal  glands.  This  fluid,  or 
musk  as  it  is  sometimes  called,  can  be  ejected  accurately  up  to  several 
feet  in  the  direction  of  aJttackers.  It  is  more  overpowering,  blinding, 
and  burning  than  that  of  Mephitis^  land  there  are  few  animals  that  are 
not  repulsed  by  it. 

Specimens  examined. — Allegany  County:  Piney  Mountain,  i/4  inil® 
N  of  U.S.  Ex)ute  40,  at  Clarysville,  1  (specimen  taken  10  February 
1964).  GaiTett  County:  Locklynn  Heights,  1  (specimen  taken  in  mid- 
January  1963). 

Other  records  and  reports. — Latham  and  Studholme  (1947,  p.  409) 
report  a  specimen  from  4  miles  west  of  Hancock,  Washington  County. 
James  H.  Beal,  of  Frostburg,  tells  me  (in  correspondence)  that  he  col- 
lected a  specimen  on  Town  Hill  (Mountain),  Allegany  County,  near 
the  beacon  light  in  August  1962,  and  another  near  the  same  locality  in 
1959.  The  following  records  are  from  Bookhout  (1964,  p.  214)  :  Green 
Ridge  Mountain  (elevation  1,400  ft.),  Allegany  Comity  (one  animal 
seen  in  December  1957)  ;  and  Dan's  Mountain  (elevation  1,600  ft.), 
Allegany  County  (four  specimens  trapped  since  1960) . 

Remarks. — The  spotted  skunk  is  essentially  a  southern  species  and 
has  apparently  extended  its  range  into  Maryland  and  Pemisylvania 
only  within  recent  years.  The  first  record  of  a  spotted  skunk  in  Penn- 
sylvania was  as  recent  as  40  years  ago  (Latham  and  Studholme,  1947, 


MAMMALS  OF  MABYLANiD 


161 


p.  409)  despite  the  fact  that  trappers,  hunters,  and  collectors  have  been 
working  in  the  Maryland  and  Pennsylvania  mountains  since  Colonial 
times. 

RIVER  OTTER 
Lutra  canadensis   lataxina   F.   Cuvier 

Lutra  lataxina  F.  Cuvier,  in  Dictionnaire  des  sciences  naturelle  .  .  . 

27:242,1823. 

Type  locality. — South  Carolina. 

General  distribution.— Constsd  Plain  and  Piedmont  of  the  eastern  United  States, 
from  western  Connecticut  and  southern  New  York,  south  to  South  Carolina. 

Distribution  in  Maryland. — ^The  species  is  statewide  in  distribution. 
The  subspecies  lataxina  inhabits  the  Eastern  Shore,  Western  Shore, 
and  Piedmont  sections,  but  may  be  replaced  by  Lutra  canadensis  cana- 
densis in  the  Ridge  and  Valley  and  Allegheny  Mountain  sections  where 
it  is  scarce  or  possibly  absent  (Bookhout,  in  correspondence) .  No  speci- 
mens are  available  to  establish  the  subspecific  identtity  of  the  western 
Maryland  otters  (if  they  occur  there),  but  since  L.  c.  canadensis  has 
been  reported  from  the  mountains  of  Virginia  to  the  south  (Handley 
and  Patton,  1947,  p.  133)  and  West.  Virginia  to  the  west  (Kellogg, 
1937,  p.  453),  western  Maryland  specimens,  if  and  when  obtained, 
proba;bly  will  prove  referable  to  L.  c.  canadensis. 


1 

7e' 

77- 

7fc- 

7 

i 

P 

W/////M^y/M// 

y/M/Z/M 

wMA 

1 

^1 

-39'- 

SCALE 
O        lO      20      30MILES 

1 

^^'i[v///v//riA 

-SS"- 

Lutra  aanadensis 

•    Specimens   examined 
O    Specimens    reported 

s^ 

w^^m^ 

W/y^/M 

-3B'- 

^^^ 

"V 

7%  ^  ^riJi'xE//^ 

1 

1 

7S* 

1 

7  7- 

1 

76" 

aoM 

Figure  53. — Distribution  of  Lutra  canadensis. 


162  NORTH  AMERICAN  FAUNA  66 

Distinguishing  characteristics. — Teeth  3/3,  1/1,  4/3,  1/2,  =  36;  size 
large;  body  slender  and  elongated;  head  small,  broad,  and  flattened; 
ears  and  eyes  small  and  rounded;  nose  broad  and  flat;  tail  long,  about 
a  third  of  the  total  length  of  the  animal,  very  heavy  at  the  base  and 
tapering  toward  the  tip;  legs  very  short,  ending  in  large  feet  with 
webbed  toes;  pelage  consisting  of  a  dense  underfur  overlaid  with  silky 
guard  hairs;  coloration  a  rich  deep  brown,  generally  somewhat  paler 
on  the  belly  and  often  with  a  grayish  mixture  on  the  lips,  chin,  and 
throat.  The  subspecies  L.  c.  canadensis  is  similar  to  the  above  but 
considerably  darker  in  coloration. 

The  combination  of  large  size,  flat,  broad  head,  thick,  heavy  tail,  and 
webbed  toes  distinguish  the  otter  from  similar  mammals  in  Maryland. 

Measurements. — No  external  measurements  are  available  for  the 
Maryland  and  District  of  Columbia  specimens  in  the  National  collec- 
tions. Handley  and  I'atton  (1947,  p.  134)  give  the  range  of  external 
measurements  in  otters  as  follows:  Total  length  900-1,200;  tail  300- 
400;  hind  foot  100-120. 

A  young  male  from  Glen  Echo,  Montgomery  County,  and  an  un- 
sexed  (but  apparently  a  male)  old  adult  from  Washington,  D.C.,  have 
the  following  cranial  measurements:  Basilar  length  95.8, 101.6;  zygo- 
matic breadth  65.3,  ;  postorbital  breadth  19.1,  20.7;  mastoidal 

breadth  62.9,  66.7 ;  length  of  maxillary  toothrow  35.2,  38.8.  Two  un- 
sexed  (but  apparently  female)  adults  from  Washington,  D.C.,  measure 
cranially :  Basilar  length  87.5, 90.6 ;  zygomatic  breadth  64.3, ;  post- 
orbital  breadth  17.2,  19.2;  mastoidal  breadth  56.7,  59.9;  length  of 
maxillary  toothrow  32.9,  34.2. 

Habitat  and  habits. — The  otter  occurs  along  rivers,  streams,  and 
lakes,  and  it  appears  to  be  quite  common  in  the  marshes  that  border  the 
Chesapeake  Bay  and  the  Atlantic  Ocean.  It  occurs  on  Assateague 
Island,  where  Jacob  Valentine,  former  manager  of  the  Chincoteague 
National  Wildlife  Refuge,  told  me  that  as  many  as  seven  were  living 
in  1958.  Most  of  these,  however,  were  in  the  Virginia  portion  of  the 
island,  on  the  Refuge. 

Maryland's  Eastern  Shore  supports  a  large  population  of  otter. 
Audubon  and  Bachman  (1851,  p.  11)  and  Coues  (1877,  p.  211)  re- 
ported them  as  common  there  in  the  19th  century.  Brayton  (1882, 
p.  58)  says  that  the  Eastern  Shore  of  Maryland  appears  to  have  always 
been  a  favorite  resort  of  the  otter.  Another  area  where  this  species  is 
abundant  is  on  the  Proving  Grounds  near  Edgewood  Arsenal,  Harford 
County. 

Otters  were  at  one  time  relatively  common  along  the  Potomac  River 
and  its  tributaries  in  the  vicinity  of  Washington,  D.C.,  and  have  often 
been  reported  from  the  city  proper.  Bailey  (1923,  p.  125)  records  an 
otter  at  the  north  end  of  Rock  Creek  Park  in  1920  and  one  taken  at 


MAMMALS  OF  MARYLAND  163 

Eastern  Branch  near  Bennings  in  1895.  In  neai^by  Maryland  he  reports 
that  otter  tracks  were  seen  on  Plummers  Island  in  1910  and  1922,  and 
that  one  was  observed  swimming  across  the  Potomac  River  near  Seneca 
in  April  1920.  Otters  still  are  not  uncommon  along  the  Potomac  River 
both  to  the  north  and  south  of  Washington.  L.  G.  Henbest  observed 
one  swimming  in  the  Potomac  near  Great  Palls  in  late  January  and 
February  1964  and  obtained  a  photograph  of  the  animal  when  it 
climbed  out  onto  a  rock  on  the  Maryland  side  of  the  river. 

The  otter  may  be  active  any  time  of  the  day  or  night,  but  tends  to 
be  more  nocturnal  than  diurnal.  Even  though  it  may  be  common,  it  is 
seldom  seen  by  the  casual  observer  because  it  is  shy  and  spends  much  of 
its  time  in  water.  These  animals  are  powerful  and  graceful  swimmers 
and  dive  with  ease  and  agility.  When  swimming  on  the  surface  it  holds 
its  head  high  out  of  the  water  and  both  the  forelegs  and  hind  limbs 
are  directed  backward,  progression  being  made  primarily  by  twisting 
and  moving  the  body  and  tail.  The  otter  can  reach  a  speed  of  6  or  7 
miles  an  hour  on  the  surface,  and  nearly  as  great  a  speed  when 
submerged. 

The  otter  inhabits  a  well  hidden  den  along  the  bank  of  the  stream 
or  river  in  which  it  lives.  According  to  Liers  (1951,  p.  4)  these  animals 
seldom  dig  their  own  dens,  but  utilize  abandoned  beaver  lodges  or 
wood-chuck  or  muskrat  burrows,  enlarging  them  to  suit  their  needs. 
Often  these  dens  are  simply  short  tunnels,  but  sometimes  they  may  be 
extensive  and  complicated.  The  main  entrance  is  always  under  water. 
In  marshes,  the  otter  may  prepare  a  nest  from  dry  marsh  grasses. 

Nothing  has  been  published  concerning  the  breeding  habits  of  otters 
in  Maryland.  Liers  (1951,  p.  4)  studied  them  in  Minnesota  under 
semiwild  conditions  and  reports  that  otters  breed  there  in  winter  and 
early  spring.  He  found  the  gestation  period  to  vary  from  9  months  18 
days  to  12  months  15  days.  Only  one  litter  is  produced  a  year,  com- 
prising generally  two  to  four  young.  The  male  is  allowed  to  rejoin 
the  family  group  after  the  young  have  left  the  nest,  and  he  assists  the 
female  in  teaching  them  to  swim  and  hunt  for  food. 

The  otter  eats  a  variety  of  foods,  but  is  primarily  carnivorous, 
consuming  crayfish,  frogs,  turtles,  larvae  of  aquatic  insects,  angle- 
worms, and  fish  (Liers,  1951,  p.  1).  Jackson  (1961,  p.  388)  says  that 
the  otter  rarely  eats  muskrat,  young  beaver,  or  duck,  and  that  the  parts 
of  land  vertebrates  occasionally  found  among  its  remains  probably 
were  eaten  as  carrion.  On  Assateague  Island  the  otters  appeared  to 
be  feeding  largely  on  jumping  mullet  {Mugil  cephalus) . 

Otter  fur  is  currently  commanding  good  prices  on  the  market,  being 
durable,  soft,  and  dense.  During  the  1965-66  trapping  season,  495  wild 
otters  were  trapped  in  Maryland  for  the  fur  market  (U.S.  Fish  and 


164  NORTH  AMERICAN  FAUNA  66 

Wildlife  Service,  Fur  Catch  in  the  United  States,  1966,  Wildlife 
Leaflet  478). 

Specimens  examined. — Montgomery  County:  Glen  Echo,  1.  District 
of  Cohimhia :  3. 

Other  records  and  reports. — Calvert  County :  Chesapeake  Bay,  near 
Stoakley  (LeCompte,  1937:  15).  Garrett  County.  Deep  Creek  Lake 
(Browning,  1928,  p.  213).  Harford  County:  Edgewood  Arsenal  area 
(personal  observation).  Montgomery  County:  Great  Falls  (identified 
from  photograph  taken  by  L.  G.  Henbest,  February  1964) .  Washing- 
ton County:  near  Leitersburg  (Washington,  D.C.,  Herald,  7  January 
1909).  Worcester  County:  Assateague  Island  (personal  observation). 

Family  FELIDAE  (cats) 

BOBCAT 

Lynx  rufus  rufus  (Schreber) 

Felis  rufa  Schreber,  Die  Saugthiere  .  .  .  ,  Thiel  3,  Heft  95,  pi.  109b, 
1777. 

Type  locality. — New  York. 

General  distribution. — In  the  eastern  United  States,  this  race  formerly  oc- 
curred from  central  New  England  south  to  northern  Georgia,  and  west  into  the 
Dakotas,  Iowa,  Kansas,  and  Oklahoma.  It  is  now  absent  or  rare  in  the  Coastal 
Plain  in  the  southern  portion  of  its  range  except  in  Virginia's  Dismal  Swamp. 

Distribution  in  Maryland. — Formerly  statewide  in  distribution,  but 
now  confined  primarily  to  the  Allegheny  Mountain  and  Ridge  and 
Valley  sections.  It  has  been  entirely  exterminated  in  the  Eastern  Shore 
section  and  is  only  rarely  encountered  in  the  Western  Shore  and  Pied- 
mont sections. 

This  species  is  uncommon  enough  in  Maryland  to  produce  local 
newspaper  accounts  when  one  is  taken. 

Distinguishing  characteristics. — Teeth  3/3,  1/1,  2/2,  1/1,  =  28; 
general  appearance  catlike,  but  considerably  larger  than  a  domestic 
cat,  averaging  about  twice  as  much  in  size  and  weight;  body  short; 
ears  prominent  and  with  small  conspicuous  tufts  on  the  tips;  eyes 
large  and  with  eliptical  pupils;  taU  very  short,  less  than  a  fourth  of  the 
total  length  of  the  animal;  pelage  fairly  long  and  loose;  coloration  of 
upperparts  grayish  to  brownish,  darker  along  the  midUne,  and  spotted 
and  blotched  throughout;  abdomen  and  inner  sides  of  legs  white, 
prominently  marked  with  black  spots;  taU  always  tipped  with  black. 

The  only  Maryland  mammal  with  which  the  bobcat  may  be  con- 
fused is  the  domestic  cat,  from  which  it  is  readily  distinguished  by 
its  larger  size  and  short  black-tipped  tail. 

Measurements. — No  external  measurements  are  available  for  Mary- 
land or  District  of  Columbia  specimens  in  the  National  collections. 


MAMMALS  OF  MARYLAND 


165 


Lynx  mfus  pufus 
•  Specimens  examined 
O  Specimens  reported 


Figure  54. — Distribution  of  Lynx  rufus  rufus. 


Kellogg  (1937,  p.  457)  gives  external  measurements  of  11  adult  males 
from  West  Virginia  as  follows:  Total  length  870  (787-935) ;  tail  146 
(133-165) ;  hind  foot  171  (162-195).  According  to  Jackson  (1961,  p. 
402)  the  male  bobcat  averages  about  10  percent  longer  than  the  female 
and  weighs  about  30  percent  more. 

A  female  from  near  Fort  Washington,  Prince  Georges  County,  has 
the  following  cranial  measurements :  Greatest  length  128.0 ;  zygomatic 
breadth  83.7;  interorbital  breadth  23.2;  maxillary  toothrow  40.4. 

Habitat  and  habits. — Bobcats  prefer  wild  heavily  wooded  or  brushy 
areas,  particularly  in  rocky  habitats  and  swamps.  In  Maryland  the 
animal  is  still  fairly  numerous  in  the  wilder  areas  of  the  Allegheny 
Mountain  and  Eidge  and  Valley  sections,  but  is  very  scarce  in  the 
rest  of  the  State.  No  specimens  have  been  taken  in  the  Eastern  Shore 
section  for  many  years,  and  presumably  the  animal  is  extirpated  there. 
According  to  Mansueti  (1950,  p.  21)  the  species  has  been  ruthlessly 
exterminated  in  Maryland  as  "vermin,"  and  is  everywhere  much  scarcer 
than  in  the  past. 

Mansueti  ( 1950,  pp.  22-23 )  has  gathered  together  a  number  of  bob- 
cat records  in  Maryland.  He  says  that  Meshach  Browning  is  reported 
to  have  killed  scores  of  bobcats  in  the  early  19th  century,  and  that 
they  were  an  everyday  occurrence  in  Garrett  County  then.  Marye 
(1945)  says  that  a  generation  ago  bobcats  were  destructive  to  sheep 
near  the  Falls  of  the  Patapasco  River,  and  that  in  his  time  they  were 


166  NORTH  AMERICAN  FAUNA  66 

occasionally  killed  in  Baltimore  County.  He  reports  that  in  the  1920's 
he  saw  a  large  bobcat  in  Day's  woods,  between  the  Great  and  Little 
Falls  of  the  Gunpowder  River.  He  also  cites  some  notes  relative  to 
the  bobcat  on  the  Eastern  Shore  and  says  that  about  2  decades  ago 
(also  in  the  1920's),  a  wild  animal  of  the  cat  family  was  treed  by  dogs 
on  the  borders  of  the  Nassawango  Swamp,  near  Nassawango  Bridge 
in  Worcester  County.  The  animal  escaped  and  Marye  doubts  that  any 
domestic  cat  could  have  done  so  under  the  circumstances  imposed. 

Mansueti  (1950,  p.  22)  quotes  an  article  from  the  Baltimore  Evening 
Sun  (18  February  1948)  entitled  "Bobcats  Still  Here,"  which  says  that 
Thomas  Leary,  hunter  of  Beans  Cover,  Allegany  County,  trapped  a 
bobcat  in  1948  on  Evitts  Mountain  in  Allegany  County  and  the  news- 
paper published  a  photograph  of  the  animal,  thus  substantiating  the 
capture. 

Mansueti  (1950,  p.  23)  says  that  John  Hamlet,  formerly  with  the 
U.S.  Fish  and  Wildlife  Service,  told  him  that  a  few  years  ago  (1945 
or  1946)  a  bobcat  was  known  to  be  roaming  the  Cypress  Swamp  region 
of  Calvert  County,  and  Watson  Perrygo  of  the  Division  of  Mammals, 
U.S.  National  Museum,  tells  me  that  bobcats  are  presently  residing 
in  wild  areas  on  his  property  near  Port  Tobacco  in  Charles  County. 

Several  interesting  specimens  of  bobcats  from  Maryland  and  the 
District  of  Columbia  are  in  the  collections  of  the  U.S.  National  Mu- 
seum. One  of  these,  a  young  female,  was  shot  along  with  five  others 
in  a  swamp  near  Oxon  Hill,  Prince  Georges  County,  in  1941  when 
the  swamp  was  being  razed  for  a  housing  development.  Another  (an 
old  female)  was  found  dead  in  December  1958  on  the  curb  of  a  down- 
town Washington  Street,  not  far  from  Rock  Creek  Park.  The  animal 
was  not  examined  for  bullet  wounds  but  probably  was  shot  in  the 
mountains  west  of  Washington  and  then  dumped  from  an  auto  onto 
the  Washington  Street,  although  it  is  remotely  possible  that  it  had 
wandered  naturally  into  downtown  Washington  via  Rock  Creek  Park. 
Bailey  (1923,  p.  121)  lists  several  bobcat  records  from  nearby  Virginia. 

The  Maryland  Conservationist  (27(1),  pp.  9,  28,  Spring  1950)  re- 
cords the  capture  of  a  particularly  large  bobcat  in  Maryland.  On  Labor 
Day  of  1949,  Frank  Wigfield  killed  the  animal  on  Iron  Mountain, 
about  5  miles  east  of  Cumberland,  Allegany  County.  It  weighed  43 
pounds  and  measured  53  inches  from  tip  to  tip. 

The  bobcat  is  shy  and  retiring,  and  primarily  solitary  in  its  habits. 
It  is  almost  entirely  nocturnal  and  is  seldom  abroad  in  daylight.  Gen- 
erally, it  seeks  shelter  under  shrubs  or  in  rock  crevices,  but  some- 
times it  dens  in  hollows  trees,  stumps,  or  logs.  The  den  is  lined  with 
grasses,  leaves,  moss,  and  other  vegetation,  which  are  scraped  and 
scratched  into  a  nest. 


MAMMALS  OF  MARYLAND  167 

Mating  in  this  species  occurs  in  February  or  March ;  the  gestation 
period  is  about  50  days,  and  between  one  and  four  kittens  are  born, 
usually  in  April.  At  birth  the  young  are  blind ;  the  eyes  open  after 
about  9  or  10  days.  Although  weaned  when  60  to  70  days  old,  the  young 
continue  with  the  mother  until  autumn  or  sometimes  late  winter. 

The  food  of  the  bobcat  is  entirely  animal  in  nature,  and  consists  to  a 
large  extent  of  rabbits  as  well  as  squirrels,  mice,  muskrats,  and  various 
kinds  of  birds.  Bobcats  often  feed  on  deer;  fawns  are  especially  vul- 
nerable prey,  and  no  doubt  deer  carrion  is  often  consumed.  Domestic 
livestock,  mainly  calves  and  sheep  but  also  occasionally  poultry,  are 
also  eaten. 

Mansueti  (1950,  p.  23)  says  that  the  bobcat  is  undoubtedly  vanish- 
ing in  Maryland,  but  its  wary  and  secretive  habits  will  insure  its  per- 
manence in  some  of  the  more  isolated  portions  of  the  State. 

Specimens  exarmned. — Prince  Georges  County:  Fort  Washington, 
near,  1 ;  Oxon  Hill,  1.  District  of  Colurnbia:  1. 

Other  records  and  reports. — Anne  Anmdel  County:  Annapolis,  3 
miles  NW  near  Severn  River  (John  C.  Lingebach,  in  verbis) .  Allegany 
County:  Evitts  Mountain  (Mansueti,  1950:  22) ;  Iron  Mountain  (Md. 
Conservationist,  27(1),  pp.  9,  28,  Spring  1950).  Baltimore  County: 
Day's  Woods  between  the  Great  and  Little  Falls  of  the  Gunpowder 
River  (Mansueti,  1950,  p.  22).  Calvert  County:  Cypress  Swamp  along 
Battle  Creek  (Mansueti,  1950,  p.  23).  Charles  County:  near  Port  To- 
bacco (W.  M.  Perry  go,  in  verbis).  Howard  County:  Falls  of  the 
Patapsco  River  (Mansueti,  1950,  p.  22).  Prince  Georges  County: 
Patuxent  River,  near  Upper  Marlboro  (Bailey,  1923,  p.  121). 
Worcester  Cou/nty:  Nassawango  Swamp,  near  Nassawango  Bridge 
(Mansueti,  1950,  p.  22). 

Order  ARTIODACTYLA  (even-toed  hoofed  mammals) 

Family  CERVIDAE  (deer) 

SIKA  DEER 

Cervus  nippon  Temminck 

Cervv^  nippon  Temminck,  Coup  d'oeil  sur  la  f  aune  des  iles  de  la  Sonde 
et  de  I'empire  du  Japon,  xxii,  1838. 

Type  locality. — Japan. 

General  distribution, — Native  to  Japan,  eastern  China,  Korea,  and  Manchuria. 
Introduced  into  England,  New  Zealand,  Denmark,  France,  Austria,  Russia, 
and  the  United  States. 

Distribution  in  Maryland. — James  Island,  Taylors  Island,  and  ad- 
jacent mainland  in  Dorchester  County,  and  Assateague  Island 
Worcester  County. 


168  NORTH  AMERICAN  FAUNA  66 

Distinguishing  characteristics. — Teeth  0/3,  1/1,  3/3,  3/3,  =  34;  size 
small;  coloration  brownish  olive  or  reddish  olive  with  the  middorsal 
area  somewhat  darker  and  forming  an  indistinct  dark  line  from  the 
forehead  to  the  rump;  underparts  somewhat  lighter;  dorsum,  parti- 
cularly posteriorly,  faintly  speckled  with  indistinct  white  blotches  in 
both  young  and  adults,  the  white  blotches  being  more  noticeable  in 
summer  than  winter;  prominent  white  rump  patch  vnih.  semierectile 
hairs;  antlers  in  male  narrow,  seldom  having  over  three  points  and 
standing  erect  over  head. 

This  species  is  distinguishable  from  the  white-tailed  deer  by  a  num- 
ber of  easily  recognizable  characters.  It  is  considerably  smaller,  aver- 
aging a  third  less  in  weight;  has  speckled  pelage  in  young  and  old  of 
both  sexes ;  has  narrower  antlers  that  stand  erect  above  the  head,  rather 
than  curAdng  forward  over  head ;  and  possesses  a  small  canine  tooth  in 
both  sides  of  upper  jaw. 

Measurements. — No  external  measurements  are  available  for  any  of 
the  Maryland  specimens.  The  species  ranges  in  shoulder  height  from 
32  to  43  inches  (Tate,  1947,  pp.  341-342) . 

Cranial  measurements  of  an  adult  male  from  James  Island,  Dor- 
chester County,  are :  Greatest  length  231 ;  zygomatic  breadth  97.1 ;  in- 
terorbital  breadth  69.3;  maxillary  toothrow  68.6.  Cranial  measure- 
ments for  two  adult  females  from  James  Island  are  as  follows :  Great- 
est length  220,  224,  zygomatic  breadth  91.3,  93.4;  interorbital  breadth 
53.0,  60.0;  maxillary  toothrow  62.5,  65.9. 

Habitat  and  habits. — In  its  natural  range,  this  species  prefers  hilly 
regions  with  mixed  large-leafed  forests.  It  does  best  in  areas  which  are 
not  subject  to  heavy  snowfall  (Flerov,  1952,  p.  128) . 

In  Maryland,  it  has  been  introduced  on  Assateague  Island,  and  on 
James  Island,  from  which  it  has  spread  to  neighboring  Taylors  Island 
and  the  adjacent  Dorchester  County  mainland.  According  to  Flyger 
(1960a),  four  or  five  sika  deer  were  released  on  James  Island  about 
1916  by  Clemment  Henry,  who  had  kept  them  in  an  enclosure  near 
Cambridge  for  an  unknown  period  before  releasing  them  on  the  island. 
They  multiplied  on  James  Island  and  spread  to  nearby  Taylors  Island, 
and  eventually  to  the  mainland.  Flyger  and  Warren  (1958)  estimated 
that  in  the  fall  of  1957,  270  sika  deer  inhabited  James  Island.  Kegard- 
ing  their  introduction  to  Assateague  Island,  Flyger  (1960a)  says  that 
Charles  Law  of  Berlin,  Md.,  stated  that  he  purchased  five  sika  deer 
(two  males  and  three  females)  from  a  man  in  Cambridge  in  1920. 
These  deer  were  held  in  an  enclosure  near  Berlin  for  several  years, 
during  which  time  three  young  were  born  and  one  of  the  original  males 
died.  Dr.  Law  sold  these  deer  to  a  man  who  in  turn  released  them  on 
Assateague  Island  where  they  have  prospered  and  grown  into  a  herd 


MAMMALS  OF  MARYLAND  160 

of  over  a  thousand  animals  (Flyger,  1964,  p.  213),  Most  of  these,  how- 
ever, are  located  in  the  southern  portion  of  the  island  in  Virginia. 

Sika  deer  can  be  hunted  in  Maryland  during  the  regular  deer  hunt- 
ing season,  and  nearly  every  year  a  few  have  been  taken  in  Dorchester 
County.  However,  these  deer  are  wilder  and  more  timid  than  native 
white-tailed  deer,  and  are  more  difficult  to  stalk.  Because  they  are 
primarily  nocturnal  in  habits  many  local  people  are  even  unaware  of 
their  existence  in  their  neighborhood. 

The  sika  deer  has  been  introduced  into  various  European  countries, 
some  of  which  are  not  pleased  with  the  species  since  it  is  too  secretive 
and  wild  to  be  a  satisfactory  game  animal,  and  has  a  propensity  for 
peeling  bark  from  trees  and  competing  with  other  species  of  deer  for 
food  (Flyger,  1959,  p.  24).  Whether  it  is  a  potential  boon  or  threat 
to  sportsmen  in  Maryland  is  still  uncertain. 

Little  is  known  of  the  biology  of  this  species  in  Maryland.  In  the 
Soviet  Union  where  the  animal  has  been  widely  introduced,  Flerov 
(1952,  pp.  128-129)  reports  that  they  are  gregarious  and  that  during 
certain  periods  their  herds  consist  of  many  dozens  of  animals.  Rutting 
begins  in  September  and  lasts  for  li/^  to  2  months.  Rutting  takes  a  very 
stormy  course  and  is  accompanied  by  roaring  and  terrific  battles.  After 
the  rut,  the  males  gather  together  in  herds  and  remain  apart  from  the 
females  during  the  entire  winter.  Females  with  2-  or  3-year-old  young 
also  gather  in  separate  groups  just  prior  to  winter.  Calving  occurs 
toward  the  end  of  May  or  June,  generally  one  fawn,  but  occasionally 
twins,  being  produced. 

These  deer  swim  readily  and  sometimes  will  cross  large  bodies  of  salt 
water.  Their  food  in  Maryland  is  probably  similar  to  that  of  the  white- 
tailed  deer,  and  it  is  feared  that  in  areas  where  the  sika  deer  becomes 
well  established  the  native  white-tailed  species  will  not  be  able  to  com- 
pete for  the  available  food  supply. 

Specimens  exaTnined. — Dorchester  County:  James  Island,  8. 

Remarks. — Presnall  (1958,  pp.  48-49)  listed  sika  deer  as  occurring 
on  Assateague  Island,  but  incorrectly  identified  the  deer  from  Dor- 
chester County  as  hog  deer  (Axis  porcinus) .  As  pointed  out  by  Flyger 
(1960a),  not  only  are  the  Dorchester  County  animals  Cervus  nipjyon, 
but  very  probably  they  derive  from  the  same  stock  as  the  Assateague 
Island  populations. 

In  addition  to  Sika  deer,  Maryland  supports  small  ix>pulations  of 
introduced  fallow  deer  {Dama  dama).  Presnall  (1958,  p.  48)  says  that 
a  few  animals  remain  from  introductions  in  Worcester  County  (Mills 
Island  in  Chincoteague  Bay)  between  1920  and  1930,  and  in  Talbot 
County  between  1935  and  1945.  Fallow  deer  are  native  to  the  Medi- 
terranean region  of  southern  Europe  and  western  Asia,  but  have  been 
widely  introduced  in  northern  Europe  and  the  United  States,  where 


170  NORTH  AMERICAN  FAUNA  66 

colonies  exist  in  Kentucky,  Tennessee,  Virginia,  and  elsewhere.  This 
deer  is  about  the  size  of  a  Maryland  wliite-tailed  deer,  but  with  large 
pahnate  antlers  which  are  dii'ected  upward.  In  sununer  pelage,  the 
coloration  is  fawn,  with  numerous  white  spots;  in  winter,  a  uniform 
grayish  (although  melanism  and  albinism  are  not  infrequent).  Miller 
(1912,  pp.  971-972)  gives  external  measurements  of  a  European  adult 
male  of  this  species  as :  Head  and  body  length  1540;  tail  190 ;  hind  foot 
( with  hoof)  435 ;  ear  from  crown  165. 

WHITE-TAILED  DEER 

Odocoileus  virgitiianus  borealis  Miller 

Odocoileus  americanus  borealis  Miller,  Bull.  New  York  State  Mus. 
Nat.  Hist.,  8 :  83, 21  November  1900. 

Type  locality. — Bucksport.  Hancock  Coxinty.  Maine- 

General  distribution. — "Western  Ontario,  east  across  southern  Quebec,  New 
Brunswick,  and  Nova  Scotia;  and  from  near  James  Bay  (Xewjwrt,  Abitibi 
River),  Gaspe  Peninsula,  and  Anticosti  Island  south  to  southern  Maryland, 
southern  Pennsylvania.  Ohio.  Indiana,  and  Illinois.  Southern  boundaries  fixed 
at  Potomac  and  Ohio  rivers  and  the  western  limits  at  the  Missi^ippi  and  Red 
Rivers."  (Kellogg.  1956.  p.  40). 

Distribution  in  Maryland.— Xt  one  time  the  white-tailed  deer  was 
nearly  extirpated  in  Maryland.  Today  it  is  common  in  all  sections  of 
the  State,  and  is  found  in  the  wilder  areas  of  every  county. 

Distiiiguishiriig  characteristics. — Size  large,  larger  than  sika  deer; 
antlers  heavy,  and  main  beam  directed  forward,  bearing  the  several 
tines  behmd ;  upper  parts  of  body  colored  reddish  brown  in  summer 
and  grayish  in  winter,  unspotted  except  in  juveniles;  underparts  and 
underside  of  tail  white ;  juvenile  animals  are  reddish  yellow  and  spotted 
with  white. 

Measiireinejit. — Kellogg  (1956,  p.  40)  gives  external  measurements 
of  the  largest  male  of  this  subspecies  that  he  examined  as :  Total  length 
2400;  tail  365:  hind  foot  538;  height  at  slioulder  1041.  Two  adult 
males  from  Cumberland,  Allegany  County,  have  the  following  cranial 

measurements:  Condylobasal  length  ,  261.8;  width  of  orbit  at 

frontojugal  suture  129.7,  120.9 ;  least  interorbital  breadth  74.2 ;  length 
of  maxillary  tootlirow  71.8,  72.5.  Females  average  smaller  than  males 
m  size. 

Flyger  (1958,  p.  8)  says  that  the  average  weight  of  47  adult  male 
deer  from  western  Maiyland  was  127.5  pounds,  and  17  from  Worcester 
County  averaged  125.4  pounds,  whereas  6  from  the  Aberdeen  Proving 
Grounds  in  Harford  County  averaged  only  104.2  jwunds.  "Wherever 
the  deer  population  becomes  so  great  that  a  scarcity  of  food  results, 
the  size  and  weight  of  the  deer  in  that  area  become  markedly  reduced. 


MAMMALS  OF  MARYLAND  171 

This  was  the  case  with  the  Aberdeen  herd,  where  at  the  time  of  Fly- 
ger's  study  deer  were  over  abundant. 

Habitat  and  habits. — Deer  are  essentially  animals  of  the  ''edges," 
preferring  burned- over  areas  and  second-growth  timber.  They  are 
much  less  common  in  heavily  forested  sections  because  the  dense  fo- 
liage discourages  the  growth  of  low  forage  on  which  the  deer  feed. 
Since  much  of  Maryland  today  consists  of  edge  habitat,  deer  are 
probably  even  more  abundant  in  the  State  than  they  were  before  the 
coming  of  the  white  man  when  most  of  the  area  was  heavily  wooded. 

Even  though  much  of  Maryland  was  heavily  forested  in  precolonial 
and  colonial  days,  white-tailed  deer  were  apparently  numerous  and 
supplied  a  good  source  of  food  for  early  settlers.  According  to  Man- 
sueti  (1950,  p.  13)  there  are  countless  references  to  the  abundance  of 
deer  in  early  letters  and  accounts  of  conditions  of  the  l7th,  18th,  and 
19th  centuries. 

Although  deer  originally  occurred  in  eveiy  Maryland  county,  the 
species  was  almost  exterminated  from  about  1900  until  the  early  1930's. 
This  was  due  apparently  to  high  hmiting  pressure  and  other  factors. 
For  example,  Browning  (1928)  estimated  that  he  killed  between  1,800 
and  2,000  deer  during  his  hunting  career  in  western  Maryland,  and 
that  by  1839  the  deer  in  Garrett  and  Allegany  counties  were  beginning 
to  become  scarce.  Other  factors  that  were  responsible  for  the  decline 
in  the  deer  herds  in  Maryland  include  wild  dog  packs  and  forest  fires, 
both  of  which  are  known  to  have  killed  many  individuals  throughout 
the  State. 

The  population  increase  in  recent  years  has  resulted  from  stocking 
and  intelligent  conservation,  as  well  as  from  the  increased  "edge" 
habitat  in  many  areas  of  the  State.  Today,  the  white-tailed  deer  oc- 
curs in  all  sections  of  Maryland,  and  in  some  places  is  overabundant. 
Such  an  area  is  the  Aberdeen  Proving  Grounds  in  Hartford  County, 
Avhere  according  to  Flyger  (1958,  p.  3)  counting  100  or  200  deer  in  a 
single  morning's  observation  is  not  at  all  unusual,  and  where  a  distinct 
browse  line  is  evident  in  the  woods.  At  the  Proving  Grounds,  also, 
there  have  been  several  instances  of  mass  die-off  in  recent  years,  an 
indication  of  overpopulation  in  a  particular  area.  Flyger  found  that 
the  deer  herd  in  Cecil  County,  on  the  other  hand,  is  still  rapidly  grow- 
ing and  the  range  there  is  more  imderstocked  than  in  any  other  part 
of  the  State. 

The  Maryland  Conservationist  (40(1),  p.  15,  Jan.-Feb.,  1963)  lists 
the  total  deer  kill  in  various  Maryland  counties  for  the  1962  season 
as  follows:  Garrett  577,  Allegany  699,  Washington  344,  Frederick 
214,  Carroll  114,  Howard  12,  Montgomery  2,  Anne  Arundel  5  Calvert 
93,  Prince  Georges  12,  Charles  208,  St.  Marys  33,  Baltimore  95,  Cecil 


172  NORTH  AMERICAN  FAUNA  66 

351,  Harford  70,  Kent  619,  Queen  Annes  124,  Caroline  106,  Talbot  180, 
Dorchester  696,  Somerset  192,  Wicomico  161,  Worcester  377.  In  addi- 
tion to  the  above,  418  deer  were  killed  at  Aberdeen  Proving  Grounds 
during  the  season.  The  Fish  and  Wildlife  Service  reports  (Big  Game 
Inventory  for  1967,  Wildlife  Leaflet  481,  September  1968)  an  esti- 
mated total  of  75,000  deer  in  the  State  for  1967. 

White-tailed  deer  are  primarily  nocturnal,  but  are  often  abroad  dur- 
ing daylight  hours.  With  regard  to  feeding  habits  of  this  species  in 
Maryland  and  the  availability  of  food  within  the  State,  Bitely  (1963, 
pp.  8-9)  says: 

Deer  require  a  varied  diet  and  if  you've  ever  watched  them  feed,  they'll 
nibble  here  and  there,  take  a  twig  of  witch  hazel,  then  red  maple,  some  huckle- 
berry and  for  dessert  some  greenbriar.  .  .  .  Whenever  possible,  they  prefer 
browse,  such  as  greenbriar,  maple  leaf  viburnum,  blueberry,  sassafras,  black  oak, 
red  maple  and  blackberry.  After  several  winters  of  heavy  browsing  these  species 
begin  to  disappear  and  the  deer  are  forced  to  shift  to  less  nutritious  food. 

During  the  winter  a  deer  requires  from  6  to  8  pounds  of  dry  browse  each 
day  for  body  and  heat  maintenance.  If  the  quality  and  quantity  of  food  is  in- 
sufficient they  become  victims  of  diseases  (especially  pneumonia)  and  parasites. 
Very  few  deer  in  this  section  of  the  United  States  ever  actually  starve  to  death ; 
disease  usually  gets  them  first. 

He  says  that  surveys  conducted  in  1962  in  western  Maryland  in- 
dicated heavy  browsing  pressure  on  the  preferred  foods.  For  instance, 
of  the  twigs  within  reach  and  available  to  deer,  the  following  percent- 
ages had  been  browsed :  Maple-leaved  viburnum,  53.9 ;  blackberry,  43.8 ; 
blueberry,  59.0;  black  birch,  38.8;  black  cherry,  14.3;  dogwood  33.9; 
greenbriar,  77.6 ;  hazelnut,  24.1 ;  red  maple,  25.9 ;  black  oak,  44.4 ;  sassa- 
fras, 54.8.  In  the  western  three  counties,  an  average  of  29  percent  of 
the  annual  growth  was  browsed  each  year.  By  contrast,  on  the  Eastern 
Shore,  only  an  average  of  6.1  percent  was  taken.  The  statewide  survey 
disclosed  that  a  total  of  58  species  of  woody  plants  had  been  browsed 
throughout  Maryland. 

The  following  life  history  notes  on  the  white-tailed  deer  are  ex- 
tracted primarily  from  Severinghaus  and  Cheatum  (1956,  pp.  57-186). 

It  is  generally  agreed  that  social  organization  in  this  species  is 
limited  to  the  family  group,  which  usually  consists  of  an  older  doe 
with  her  fawns,  sometimes  including  those  of  the  previous  year. 
Leadership  of  the  group  appears  to  rest  with  the  old  doe.  The  oc- 
casional antlered  buck  that  may  be  seen  with  the  family  group  is 
usually  the  yearling  offspring  of  the  old  doe.  In  the  Northern  States, 
the  breeding  season  begins  in  November  and  the  young  are  bom  in 
May  or  June.  Antlers  begin  to  appear  on  the  bucks  in  the  summer. 
They  grow  from  a  pedicle  of  the  frontal  bone  and  are  covered  with  a 
true  skin  (the  velvet)  during  their  growth.  Antler  growth  is  rapid. 


MAMMALS  OF  MARYLAND  173 

usually  full  size  being  achieved  within  4  months  or  less.  During  the 
period  of  antler  growth,  the  buck  is  very  careful  of  the  sensitive 
appendages,  but  after  full  size  is  reached,  the  velvet  is  scraped  away, 
and  the  polished  antlers  are  used  by  the  bucks  in  battles  for  mates. 
The  necks  of  the  bucks  also  swell  considerably  during  the  mating  sea- 
son. After  the  mating  season  the  antlers  are  shed,  usually  in  January 
or  early  February  in  Northern  States,  then  the  cycle  continues. 

Gestation  period  in  this  species  varies  from  189  and  222  days,  with 
the  average  being  about  201  days.  The  usual  number  of  young,  for 
older  does,  is  two,  occasionally  three.  A  young  doe,  however,  usually 
gives  birth  to  only  a  single  offspring.  The  fawns  are  spotted,  and  re- 
main in  thickets  where  they  blend  perfectly  with  the  dappled  shadows 
of  the  foliage.  Both  bucks  and  does  generally  achieve  sexual  maturity 
at  18  months  of  age,  although  well-nourished  doe  fawns,  at  least  in 
northern  areas,  may  breed  at  6  to  8  months  of  age. 

SpecvmeTis  examined. — Allegany  County:  Cumberland,  3. 

Other  records  and  reports. — Wliite-tailed  deer  have  been  reported 
from  every  county  in  Maryland. 

Remarks. — The  subspecies  of  white-tailed  deer  that  originally  in- 
habited Maryland  was  Odocoileus  v.  borealis.  By  the  turn  of  the 
present  century,  however,  the  species  was  nearly  extinct  in  Maryland, 
as  well  as  in  most  other  eastern  States.  Widespread  transplanting  of 
deer  from  areas  in  which  they  were  still  abundant  reestablished  east- 
ern herds.  Deer  from  many  areas,  and  representing  a  number  of  sub- 
species, were  brought  into  Maryland,  and  consequently  today  it  is 
impossible  to  assign  the  State's  deer  to  any  specific  subspecies.  Accord- 
ing to  Hosley  (1956,  p.  228)  :  "One  effect  of  the  widespread  trans- 
planting of  Lake  States  deer  into  the  south  and  east  and  of  other 
similar  moves  has  been  to  mix  up  thoroughly  the  races  existing  in 
most  of  the  deer  range." 


MARINE  MAMMALS  OF  MARYLAND 

The  following  list  of  marine  mammals  comprises  only  those  that 
have  stranded  on  Maryland  beaches,  or  have  been  observed  in  waters 
off  the  Maryland  coast  and  in  Chesapeake  Bay.  The  list  does  not  in- 
clude all  the  marine  mammals  that  may  occur  in  Maryland  waters, 
and  many  additional  species  will  eventually  be  discovered.  Some  of 
these  unrecorded  species  have  stranded  on  beaches  to  the  north  and 
south  of  Maryland  and  must  also  pass  through  Maryland  waters. 
Only  those,  however,  which  have  actually  been  reported  from  the 
State  will  be  discussed  in  any  detail. 

336-897  O — 69 -12 


174  NORTH  AMERICAN  FAUNA  66 

Order  PINNIPEDIA  (pinnipeds) 

Family  PHOCIDAE  (earless  seals) 

HARBOR  SEAL 
Phoca  vitulina  concolor  De  Kay 

Phoca  concolor  De  Kay,  Zoology  of  New  York  .  .  .  ,  Vol.  1,  pt.  1 
(Mammalia) ,  p.  53, 1842. 

Type  locality. — Long  Island  Sound,  near  Sands  Point,  Nassau  County,  N.Y. 

General  distribution. — Along  the  Atlantic  coast  of  North  America  from 
Ellesmere  Island  to  South  Carolina,  but  is  rare  in  the  northern  and  southern 
portion  of  this  range. 

Description. — ^A  small  seal  that  averages  in  total  length  about  4 
or  5  feet  and  weighs  75  to  150  pounds.  The  pelage  is  coarse  and  varies 
from  yellowish  gray,  spotted  with  dark  brown  to  almost  black,  spotted 
with  yellowish.  The  spotted  pelage  and  small  size  are  distinctive  char- 
acters of  this  species. 

Maryland  records. — Harbor  seals  in  Maryland  waters  are  stragglers ; 
they  are  not  indigenous  to  the  State.  Mansueti  (1950,  pp.  28-29;  1955, 
p.  2)  summarizes  Maryland  records  as  follows:  One  specimen  taken 
in  a  seine  in  Chesapeake  Bay  near  Elkton  in  August  1824;  one  animal 
feeding  around  Thomas  Pouch  Lighthouse,  near  Annapolis,  in  March 
1894 ;  one  animal  killed  in  Tangier  Sound  on  8  July  1898 ;  one  specimen 
sighted  on  14  September  1898  on  a  beach  above  reach  of  heavy  waves 
at  Ocean  City,  Worcester  County ;  several  animals  in  Choptank  River 
near  Tilghman  Island  in  the  early  part  of  February  1925 ;  one  specimen 
seen  in  Chesapeake  Bay  at  Flag  Pond  in  1940;  one  animal  sighted  at 
Ocean  City,  Worcester  County,  in  May  1955. 

In  addition,  there  is  a  fragmentary  skin  and  partial  skeleton  of  a 
harbor  seal  in  the  National  collections ;  the  specimen  was  found  on  the 
beach  at  Assateague  Island,  3  miles  south  of  Ocean  City,  Worcester 
County,  on  12  May  1959. 

HOODED  SEAL 
Cystophora  cristata  (Erxleben) 

IPhoca^  cristata  Erxleben,  Systema  regni  animalis  .  .  .  ,  1 :  590, 1777. 

Type  locality. — Southern  Greenland  or  Newfoundland. 

General  distribution. — North  Atlantic  coast  from  Greenland  to  Labrador. 
Newfoundland,  Nova  Scotia,  and  Gulf  of  St.  Lawrence,  south  as  an  accidental  to 
Florida. 

Description. — A  large  seal,  with  males  ranging  up  to  10  feet  in  total 
length  and  weighing  up  to  850  pounds.  Females  are  smaller,  averaging 
about  8  feet  in  length  and  weighing  up  to  400  pounds.  Coloration  slate- 


MAMMALS  OF  MARYLAND  175 

gray  to  blackish  dorsally,  with  sides  paler  and  spotted  with  white. 
Males  have  a  bladderlike  protuberence  on  the  nose  which  they  can 
inflate  in  times  of  anger  or  danger. 

Maryland  records. — One  recorded  in  1865  as  taken  near  Cambridge, 
Dorchester  County,  on  an  arm  of  the  Chesapeake  Bay,  18  miles  from 
salt  water  (Cope,  1865,  p.  273) ;  one  animal  killed  at  Worton  Point, 
near  Chestertown,  Kent  County,  about  1860  (Mansueti,  1950,  p.  31). 

It  is  possible  that  the  seal  from  Tangier  Sound  previously  listed  as 
Phoca  vitulina  corwolor  may  have  been  a  hooded  seal  rather  than  a 
harbor  seal.  The  Baltimore  Sun  of  9  July  1898,  which  reported  the 
killing  of  the  animal  on  8  July  1898,  said  that  it  measured  almost  6i/^ 
feet  in  length.  If  this  measurement  was  accurate,  the  animal  would  fall 
within  the  size  range  of  the  hooded  seal  rather  than  the  harbor  seal. 

Order  CETACEA  (cetaceans) 

The  order  Cetacea  is  divisible  into  two  distinct  suborders  distin- 
guished primarily  by  the  presence  of  teeth,  or  baleen  in  the  mouth. 
Those  that  are  toothed  are  classified  as : 

Suborder  ODONTOCETI  (toothed  whales) 

Toothed  whales  may  have  teeth  in  the  lower  jaws  only,  or  in  both 
upper  and  lower  jaws.  In  some  forms  more  than  100  teeth  are  present, 
while  in  others  the  teeth  may  be  reduced  to  2.  Whales  of  this  suborder 
never  possess  baleen. 

Family  ZIPHIIDAE  (beaked  whales) 

GOOSE-BEAKED  WHALE 

Ziphius  cavirostris  G.  Cuvier 

Ziphius  cavirostris  G.  Cuvier,  Recherches  sur  les  ossemens  fossiles . . . , 
ed.  2, 5 :  352, 1823. 

Type  locality. — Near  Fos,  Bouches-du-Rhone,  France. 

General  distribution. — In  the  western  North  Atlantic,  reported  from  Newi>ort, 
Rhode  Island,  south  to  St.  Simon  Island,  Ga. 

Description. — A  medium-sized  whale,  ranging  up  to  28  feet  in  length. 
The  body  is  thickset  and  has  a  strongly  marked  median  keel  extending 
from  the  dorsal  fin  to  the  tail.  The  color  pattern  is  extremely  variable; 
the  back  is  usually  a  purplish  black  and  the  underparts  white.  Males 
have  a  single  tooth  projecting  an  inch  or  more  beyond  the  gum  at  the 
end  of  each  lower  jaw. 

Maryland  records. — On  5  September  1959,  a  whale  of  this  species  was 
sighted  alive  north  of  Fen  wick  Island,  Del.  It  stranded  that  night  at 


176  NORTH  AMERICAN  FAUNA  66 

Maryland  Beach,  Worcester  County.  This  is  the  only  Maryland 
record,  although  specimens  have  stranded  at  other  localities  to  the 
north  and  south  of  the  State. 

Family  PHYSETERIDAE  (sperm  whales) 

SPERM  WHALE 

Physeter  catodon  Linnaeus 

'IPhyseter]  ca^<?c?07i  Linnaeus,  Syst.  Nat.,  ed.  10, 1 :  76, 1758. 

Type  locality. — Kairston,  Orkney  Islands,  Scotland  (by  restriction,  Thomas, 
Proc.  Zool.  Soc.  London,  p.  157,  22  March  1911). 

General  distribution. — In  western  North  Atlantic  from  Iceland  and  Davis 
Straits,  south  to  Gulf  of  Mexico,  West  Indies,  Lesser  Antilles,  and  coast  of 
Venezuela. 

Description. — This  species  is  the  largest  of  the  toothed  whales,  males 
sometimes  reaching  a  length  of  60  feet  or  more.  Females  are  consid- 
erably smaller,  generally  under  40  feet  in  length.  In  coloration  this 
whale  is  a  uniform  gray  or  dark  bluish  gray.  The  narrow  lower  jaw 
contains  20  to  30  heavy  teeth.  Usually  no  teeth  are  visible  in  the  upper 
jaws.  There  is  no  dorsal  fin. 

Maryland  records. — Only  one  sperm  whale  is  known  to  have 
stranded  on  a  Maryland  beach.  It  came  ashore  at  Greeil  Run  Inlet 
(now  closed)  just  north  of  the  Maryland- Virginia  boundary  on 
Assateague  Island  in  December  1891.  This  specimen  is  preserved  as  a 
skeleton  in  the  U.S.  National  Museum. 

At  times,  sperm  whales  are  numerous  off  Ocean  City.  They  attract 
the  attention  of  passing  boats  by  their  habit  of  raising  their  flukes  clear 
of  the  water  when  sounding. 

PIGMY  SPERM  WHALE 

Kogia  breviceps  (Blalnville) 

Physeter  hreviceps  Blainville,  Ann.  d'Anat.  et  de  Physiol.,  2:  337, 
1833. 

Type  locality. — Region  of  Cape  of  Good  Hope,  Republic  of  South  Africa. 

General  distribution. — In  western  North  Atlantic  recorded  from  Halifax  Har- 
bor, Nova  Scotia,  south  to  Jupiter  Inlet,  Florida.  This  is  a  pelagic  species  that  is 
seldom  found  stranded  on  beaches. 

Description. — A  small  edition  of  its  larger  relative  the  sperm  whale, 
the  pigmy  sperm  whale  ranges  in  length  from  9  to  13  feet.  In  colora- 
tion it  is  black  above,  white  beneath.  There  are  usually  14  or  15  small 
needlelike  teeth  in  each  lower  jaw ;  no  teeth  visible  in  upper  jaws.  This 
species,  unlike  the  large  sperm  whale,  possesses  a  small  dorsal  fin. 


MAMMALS  OF  MARYLAND  177 

Maryland  records. — The  pygmy  sperm  whale  is  known  from  Mary- 
land by  a  live  specimen  that  came  ashore  at  Ocean  City,  Worcester 
County,  in  August  1959.  Vacationers  at  the  beach  repeatedly  tried  to 
push  the  small  whale  back  to  sea.  Eventually,  during  a  high  tide  the 
animal  worked  its  way  into  deeper  water  where  it  struggled  away. 
The  stranding  of  this  whale  is  discussed  in  detail  by  Manville  and 
Shanahan  (1961,  pp.  269-270). 

Family  DELPHINIDAE  (porpoises  and  dolphins) 
ATLANTIC  DOLPHIN 
Delphinus  delphis  Linnaeus 

[Delphiniis]  delphis  Linnaeus,  Systema  naturae,  ed.  10,  1 :  77,  1758. 

Type  locality. — European  seas. 

General  distribution. — In  western  North  Atlantic  recorded  from  Iceland  and 
Woods  Hole,  Massachusetts,  south  to  Bahama  Islands  and  Jamaica. 

Description. — This  is  a  small  Cetacean,  reaching  a  length  of  about 
8  feet.  The  animal  possesses  a  slender  "beak"  about  6  inches  long, 
which  is  sharply  marked  off  from  the  sloping  forehead  by  a  deep 
V-shaped  groove.  The  mouth  contains  many  sharp  pointed  teeth  that 
interlock  perfectly  and  are  adapted  for  catching  and  holding  the 
fish  upon  which  the  dolphin  preys.  In  coloration,  this  species  is 
blackish  dorsally,  including  the  dorsal  surfaces  of  the  flukes  and 
pectoral  apendages.  The  sides  shade  in  coloration  to  a  grayish  green, 
mixed  with  eliptical  bands  of  whitish  on  the  flanks.  The  abdomen  is 
white  and  there  is  a  whitish  band  over  the  forehead  with  a  narrow 
black  band  in  the  center  that  connects  the  black  eye  rings.  Often  there 
is  a  black  band  from  the  snout  to  the  leading  edge  of  the  pectoral  fin. 

Marlyamd  records. — No  records  of  strandings  of  this  species  are 
available  from  Maryland,  but  Charles  O.  Handley,  Jr.,  says  (unpub- 
lished manuscript)  :  "In  September  1959,  Mike  Freeman  of  Washing- 
ton, D.C.,  told  me  of  having  seen  two  kinds  of  porpoises  in  imusual 
abundance  off  Ocean  City,  Md.,  and  running  the  Ocean  City  Inlet  into 
Sinepuxent  Bay.  His  descriptions  indicated  Tursiops  truncatus  and 
Delphinus  delphis.'''' 

This  cetacean  is  probably  one  of  the  most  abundant  in  Maryland 
waters,  but  it  prefers  deeper  waters  off  shore,  and  hence  is  less  likely 
to  strand  than  several  other  less  numerous  species. 

BOTTLE-NOSED  PORPOISE 

Tursiops  truncatus  (Montague) 

Delphinus  truncatus  Montague,  Mem.  Wermerian  Nat.  Hist.  Soc, 
3 :  75,  1821. 


178  NORTH  AMERICAN  FAUNA  66 

Type  locality. — Totness,  Devonshire,  England. 

General  distribution. — In  the  western  North  Atlantic  recorded  from  Massa- 
chusetts south  to  Florida. 

Description. — Adults  of  this  species  reach  a  length  of  11  or  12  feet, 
and  may  be  recognized  by  the  purplish  lead-gray  coloration  of  the 
upper  parts,  the  short  beak,  seldom  more  than  3  inches  long,  and  the 
lower  jaw,  which  is  slightly  longer  than  the  upper.  There  are  20  to 
26  teeth  on  each  side  in  both  jaws  of  the  mouth. 

Maryland  records. — True  (1890,  p.  197)  says  that  he  has  been 
informed  that  this  species  ascends  the  Potomac  River  as  far  as  Gly- 
mont,  a  fishing  station  on  the  Maryland  shore  about  18  miles  below 
Washington,  B.C. 

On  27  and  28  July  1884,  a  porpoise,  presumed  to  be  of  this  species, 
was  observed  in  the  Potomac  River  above  the  Aqueduct  Bridge  in 
Washington,  D.C.  It  was  chased  by  boats  and  shot  at  repeatedly,  but 
not  captured.  The  species  has  been  seen  at  various  times  near  Alex- 
andria (unsigned  note  in  The  Pastime,  3(2),  p.  14,  August  1884). 

In  the  Chesapeake  Bay,  Tursiops  has  been  reported  as  far  up  as 
Havre  de  Grace,  Harford  County  (Maryland  Tidewater  News,  8, 
p.  40, 1952). 

Specimens  in  the  National  collections  are  from  the  following  Mary- 
land localities:  Point  Lookout,  St.  Mary's  County;  Queenstown 
Creek,  Queen  Annes  County ;  and  Scientist's  Cliffs,  Calvert  County. 

In  addition,  bottle-nosed  porpoises  are  often  seen  off  Ocean  City, 
Worcester  County,  and  swimming  in  the  Ocean  City  Inlet  into  Sine- 
puxent  Bay.  This  is  probably  the  most  abundant  marine  mammal  in 
Maryland  waters. 

Suborder  MYSTICETI  (baleen  whales) 

Whales  of  this  suborder  do  not  possess  teeth.  Instead,  they  are 
equipped  with  whalebone,  or  baleen,  which  hangs  down  in  the  mouth 
from  either  side  of  the  upper  jaws  in  long  strips,  with  hairlike  bristles 
on  the  inner  edges.  The  apparatus  thus  formed  serves  as  a  strainer. 
In  feeding,  the  baleen  whales  swim  open-mouthed  through  swarms  of 
plankton;  then  closing  the  mouth,  they  press  the  tongue  against  the 
baleen  plates,  squeezing  out  the  water  and  leaving  the  plankton  inside 
the  mouth  to  be  swallowed. 

Family  BALAENOPTERIDAE  (fin-backed  whales) 

LITTLE  PIKED  WHALE 

Balaenoptera  acutorostrata  Lacepede 

Balaenoptera  acutorostrata  Lacepede,  Histoire  naturelle  des  Oetacee 
.  .  .  ,  p.  37, 1804. 


MAMMALS  OF  MARYLAND  179 

Type  locality. — European  seas. 

General  distribution. — Adults  of  this  species  apparently  winter  in  tropical  or 
warm  temperate  waters,  and  summer  in  cold  temperate  and  boreal  waters. 
Young  animals,  however,  may  frequent  warm  or  temperate  waters  during  the 
summer  months.  In  the  western  North  Atlantic,  adults  have  been  reported  during 
the  summer  from  Iceland  and  Greenland  south  to  New  Jersey  and  the  Delaware 
River.  There  are  records  of  this  species  in  Florida  waters  during  winter  months, 
(see  Schwartz,  1962,  pp.  206-209). 

Description. — ^The  little  piked  whale  resembles  a  small  fin-backed 
whale  in  appearance,  but  is  of  somewhat  stouter  build.  Adults  reach 
a  length  of  about  30  feet.  There  are  approximately  50  ventral  grooves 
in  the  throat  region,  and  the  baleen  is  entirely  yellowish  white  in  color. 
The  body  is  blue-gray  on  the  back  and  white  on  the  abdomen. 

Maryland  records. — ^This  species  has  been  recorded  from  Maryland 
only  once.  On  12  July  1959,  an  immature  female  stranded  at  Dares 
Beach,  Calvert  County,  in  Chesapeake  Bay.  Schwartz  (1962)  dis- 
cusses this  specimen  and  its  stranding  in  detail. 

FIN-BACKED  WHALE 
Balaenoptera  physalus  (Linnaeus) 

\Balaena]  physalus  Linnaeus,  Systema  naturae,  ed.  10,  1 :  75,  1758. 

Type  locality. — Spitzbergen  Seas  ( See  Thomas,  Proc.  Zool.  Soc.  London,  1911, 
pt.  1,  p.  156,  22  March  1911) . 

General  distribution. — In  western  North  Atlantic,  from  Iceland  and  Greenland 
south  to  the  Gulf  of  Mexico  and  Caribbean  Sea. 

Description. — This  is  a  large  baleen  whale,  the  adults  measuring  be- 
tween 50  and  65  feet  in  total  length.  The  coloration  is  velvety  black 
except  for  a  small  ash-colored  area  at  the  tip  of  the  lower  jaws,  a 
cream-colored  chin  and  throat  and  occasionally  white  or  piebald  under- 
parts.  The  undersurface  of  the  body  in  the  region  of  the  throat  has 
numerous  longitudinal  grooves.  The  dorsal  fin  is  high  and  triangular, 
usually  with  a  concave  posterior  border.  The  baleen  in  this  species  ex- 
hibits asymmetry  in  coloration,  the  blades  on  the  right  side  being  white 
for  more  than  a  third  of  the  distance  from  the  tip  of  the  snout  and  the 
remainder  on  that  side,  and  all  of  the  left  side,  being  colored  a  dull 
blue-gray  with  streaks  of  white  and  yellow.  This  whale  is  known  as  the 
greyhound  of  the  ocean  because  of  its  slender  build  and  great  speed 
in  swimming. 

Maryland  records. — ^The  type  specimen  of  Sihhaldius  tectirostris 
Cope  (a  species  now  regarded  as  a  synonym  of  Balaenoptera  physalus) 
washed  ashore  on  the  Maryland  coast  near  Sinepuxent  Inlet,  Worces- 
ter County,  in  the  winter  1868-69.  The  skull  of  this  specimen  is  now 
in  the  U.S.  National  Museum  collections. 


180  NORTH  AMERICAN  FAUNA  66 

There  is  a  report  in  the  Maryland  Tidewater  News  (1953)  that  a 
whale  60  feet  in  length  was  stranded  at  Ocean  City,  Worcester  County, 
in  the  spring  of  1953  which  probably  was  of  this  species. 

Fin-backed  whales  are  more  numerous  off  the  Maryland  coast  than 
these  two  stranding  records  would  indicate. 

BLUE  WHALE 
Balaenoptera  musculus  (Linnaeus) 

[BaZaena]  musculiis  Linnaeus,  Systema  naturae,  ed.  10,  1 :  76,  1758. 

Type  locality. — Firth  of  Forth,  Scotland  (see  Thomas,  Proc.  Zool.  Soc.  London, 
1911,  pt.  1,  p.  156,  22  March  1911) . 

General  distribution. — ^In  the  western  North  Atlantic,  from  Iceland  and  Green- 
land south  to  Panama. 

Description. — ^This  is  the  largest  animal  that  ever  lived,  either  on 
land  or  in  water.  Adults  sometimes  reach  lengths  in  excess  of  100  feet, 
the  largest  specimens  usually  being  females.  The  color  of  this  species 
is  slate  blue  over  the  whole  body  with  the  exception  of  the  tip  and 
undersurface  of  the  flippers,  where  pigmentation  is  absent.  The  blue 
coloration  may  be  modified  by  a  pale  mottling  that  is  sometimes  dif- 
fused and  sometimes  concentrated  in  patches  in  different  parts  of  the 
body.  There  are  between  80  and  100  ventral  throat  grooves  and  the 
baleen  in  the  mouth  is  jet  black. 

Maryland  records. — ^This  species  is  known  from  Maryland  by  a  sin- 
gle specimen  that  grounded  near  Crisfield,  Somerset  County,  in  the 
summer  of  1876.  The  skeleton  of  this  juvenile  individual,  identified  by 
G.  S.  Miller,  Jr.,  is  now  in  the  museum  of  the  Natural  History  Society 
of  Maryland  in  Baltimore. 

Remarks  on  Maryland  Marine  Mammals 

The  above  list  is  composed  only  of  species  that  have  stranded  or  been 
observed  off  the  Maryland  coast.  Many  other  species  undoubtedly  pass 
through  Maryland  waters  and  will  someday  be  recorded  for  the  State. 
Some,  such  as  the  short-finned  blackfish  {Glohicepliala  Trmcrorhyncha) 
and  the  Atlantic  blackfish  {Glohicephala  melaena) .,  have  stranded  on 
beaches  only  a  few  miles  south  of  the  Maryland  State  line.  The  follow- 
ing is  a  list  of  species,  presently  unrecorded  for  the  State,  which  prob- 
ably occur  at  some  time  or  other  in  Maryland  waters : 

Harp  seal,  Phoca  groerdandica  Erxleben. 

Dense-beaked  whale,  Mesoplodon  densirostris  (Blainville) . 

Gulf  Stream  beaked  whale,  Mesoplodon  europaeus  (Gervais). 

Northern  beaked  whale,  Mesoplodon  mirus  True. 

Striped  porpoise,  Stenella  coeruleoaTbus  (Meyen) . 


MAMMALS  OF  MARYLAND  181 

Atlantic  killer  whale,  Grampus  Orcinus  (Linnaeus) . 

Atlantic  blackfishj  GlobicefhoU^  nielaena  (Traill) . 

Short-finned  blackfish,  GloMcephala  macrorJiyncha  Gray. 

Harbor  porpoise,  Phocoena  phocoena  (Linnaeus). 

Sei  whale,  Balaenoptera  horecMs  Lesson. 

Hump-backed  whale,  Megaptera  novaeangliae  (Borowski) . 

Right  whale,  Eubcdaena  glacialis  (Borowski) . 

EXTIRPATED  RECENT  MAMMALS  OF 

MARYLAND 

Mansueti  (1950)  has  discussed  in  detail  the  extirpated  Recent  mam- 
mals of  the  State.  He  lists  six  species  that  at  one  time  occurred  within 
Maryland  but  have  vanished  since  the  coming  of  the  white  man.  As 
pointed  out  by  Handley  and  Patton  (1947,  p.  78)  : 

Though  it  is  regretable  that  man  has  had  a  hand  in  the  extinction  of  these 
creatures,  he  is  not  to  be  blamed  too  much,  for  the  ascendency  of  one  species  and 
the  extinction  of  another  is  a  regular  process  of  nature  which  has  been  repeated 
over  and  over  again  all  down  through  the  ages.  Probably  man  did  not  have  much 
or  anything  to  do  with  the  disappearance  of  wild  horses,  mammoths,  mastodons, 
tapirs,  wild  pigs,  ground  sloths  and  camels  which  once  roamed  our  lands,  but 
they  are  gone  nevertheless.  As  surely  as  a  species  of  animal  comes  into  being, 
it  is  destined  to  eventual  extinction,  whether  by  geologic  catastrophies  such  as 
volcanic  eruptions  or  earthquakes ;  or  by  great  climatic  changes  involving  vast 
spreading  glaciers  or  desert  wastes,  or  by  the  hand  of  man.  Our  geologists  have 
given  us  proof  of  all  this  by  the  fossil  record  in  the  rocks. 

The  six  species  of  extirpated  Recent  mammals  of  Maryland  dis- 
cussed by  Mansueti  ( 1950)  are : 

PORCUPINE 
Erethizon  dorsatum  (Linnaeus) 

This  species  apparently  never  was  widely  distributed  in  Maryland, 
nor  was  it  ever  abundant.  Mansueti  cites  records  from  Allegany 
County ;  Blue  Ridge  Mountains ;  Frederick -Washington  Counties ;  and 
EUicott  City,  Howard  County  (all  of  these  prior  to  1881).  Rhoads 
(1903,  p.  115)  cites  porcupine  records  from  Fulton  and  Somerset  Coun- 
ties, Pa.,  adjacent  to  Maryland  on  the  north.  The  Cumberland  (Mary- 
land) Sunday  Times  for  9  August  1964  reported  that  recently  a  por- 
cupine was  shot  on  a  farm  at  Rocky  Gap,  east  of  Cumberland.  A  pho- 
tograph of  this  animal  accompanied  the  news  release.  This  may  repre- 
sent a  valid  state  record,  or  the  animal  may  have  been  brought  to 
Maryland  from  elsewhere.  This  same  article  in  the  Cumberland  Sun- 
day News  reports  that  in  1912  a  boy  in  Frostburg  brouglit  some  quills 


182  NORTH  AMERICAN  FAUNA  66 

to  school  from  a  porcupine  he  found  dead  on  Mount  Savage,  It  also 
says  that  during  the  fall  of  1948  a  hunter  reported  his  dogs  found  a 
porcupine  on  Martins  Mountain  for  they  returned  to  him  with  their 
noses  full  of  quills.  He  was  not  able,  however,  to  locate  the  porcupine. 
The  foregoing  serves  to  show  that  there  are  records  and  reports  of  the 
porcupine  in  the  western  part  of  Maryland  right  up  to  the  present 
day.  The  general  consensus  of  opinion,  however,  regarding  the  status 
of  this  animal  is  that  it  is  no  longer  a  native  inhibtant  of  the  State. 

GRAY  WOLF 
Canis  lupus  Linnaeus 

The  gray  wolf  originally  inhabited  the  entire  State  of  Maryland. 
Not  only  are  there  documents  and  publications  to  show  that  they  were 
at  one  time  statewide  in  distribution  (see  Mansueti,  1950,  pp.  25-26), 
but  the  early  settlers  used  the  name  "wolf"  to  designate  many  places 
throughout  the  State.  The  Gazeteer  of  Maryland  (Maryland  State 
Planning  Comm.,  and  Dept.  of  Geology,  Mines  and  Water  Resources, 
October  1941,  p.  230)  lists  the  following  place  names  in  Maryland 
that  give  a  good  idea  of  where  early  colonists  found  wolves :  Allegany 
County:  Wolf  Gap,  Wolf  Rock ;  Baltimore  County :  Wolf  trap  Branch ; 
Caroline  County:  Wolf  pit  Branch;  Carroll  County:  Wolfpit  Branch; 
Frederick  County:  Wolf  Rock ;  Garrett  County :  Wolf  Den  Run,  Wolf 
Gap,  Wolf  Swamp;  Somerset  County:  Wolf  Trap  Creek.  Mansueti 
(1950,  p.  25)  says  that  they  even  abounded  on  Assateague  Island  in 
Worcester  County. 

All  evidence  seems  to  indicate  that  the  gray  wolf  Avas  exterminated 
in  Maryland  at  a  very  early  date,  except  for  those  in  more  inaccessible 
parts  of  western  mountains.  Here  the  species  probably  persisted  until 
late  in  the  19th  century,  and  perhaps  even  to  the  early  part  of  the 
present  century. 

MARTEN 

Martes  americana  (Turton) 

The  marten  was  exterminated  in  Maryland  as  far  back  as  85  years 
ago.  It  apparently  was  not  widespread  in  distribution,  and  never 
abundant.  Heavy  trapping  pressure  and  destruction  of  suitable  forest 
habitat  appear  to  account  for  its  demise.  It  was  probably  most  abun- 
dant in  the  western  part  of  the  State,  but  there  are  reports  from  the 
District  of  Columbia  and  perhaps  St.  Marys  County  (see  Mansueti, 
1950,  p.  23). 


MAMMALS  OF  MARYLAND  183 

MOUNTAIN  LION 
Felis  concolor  Linnaeus 

This  species  at  one  time  occurred  throughout  the  State,  wherever 
there  were  white-tailed  deer,  which  served  as  it  principal  food.  The 
mountain  lion  was  hunted  with  relentless  energy  by  settlers  and  at  very 
early  date  was  exterminated  from  all  but  the  wildest  portions  of  the 
western  part  of  the  State.  The  date  when  the  last  mountain  lion  was 
killed  in  Maryland  is  not  known,  but  it  was  probably  sometime  toward 
the  end  of  the  19th  century.  In  the  18th  century,  the  species  appears 
to  have  been  abundant  in  the  mountains  of  Maryland.  Meshach  Brown- 
ing (1928)  estimated  that  he  killed  more  than  50  of  them  during  his 
active  period  as  a  hunter  in  Garrett  County  from  1790  to  1836.  There 
is  no  question  that  today,  however,  the  species  is  extinct  in  Maryland 
despite  the  fact  that  from  time  to  time  there  are  reports  of  them  in 
some  of  the  more  remote  portions  of  the  State.  None  of  these  recent  re- 
ports of  mountain  lions  in  Maryland  have  ever  been  verified,  and  it 
seems  that  the  species  has  been  extirpated  in  the  entire  Eastern  United 
States,  with  the  exception  of  Florida  where  a  few  still  persist  in  the 
swamps  and  hammocks  in  the  Everglades. 

WAPITI  OR  ELK 
Cervus  canadensis  (Erxleben) 

This  species  was  at  one  time  statewide  in  distribution.  Mansueti 
(1950,  pp.  11-12)  lists  a  number  of  early  references  to  it,  not  only  from 
the  mountains  of  the  west,  but  also  in  the  Tidewater.  Its  former  oc- 
currence within  the  State  is  attested  to  by  the  number  of  places  that 
bear  the  name  "elk."  Thus,  there  is  an  Elklick  Run  in  Anne  Arundel 
County,  Elklick  Run  in  Garrett  County,  Elk  Mills,  Elk  Neck,  Elk 
River,  and  Elkton  in  Cecil  County,  Elk  Mountain  and  Elkridge  in 
Washington  County,  Elkridge  in  Harford  County,  Elkridge  in  How- 
ard County,  and  Elkridge  in  Baltimore  County.  The  last  of  Mary- 
land's wapiti  were  apparently  exterminated  long  before  the  middle 
of  the  19th  century.  McAtee  (1918,  p.  52)  places  the  date  of  their 
extirpation  in  Virginia  as  1844. 

BISON 

Bison  bison  (Linnaeus) 

According  to  Mansueti  (1950,  p.  10)  the  distribution  of  bison  in 
Maryland  and  the  District  of  Columbia  must  have  been  above  the  fall 
line.  The  bison  thus  was  an  inhabitant  of  the  Piedmont,  Ridge  and 
Valley,  and  Allegheny  Mountain  sections  of  the  State.  When  the  first 
settlers  arrived,  however,  the  species  was  already  becoming  scarce,  and 


184  NORTH  AMERICAN  FAUNA  66 

these  settlers  hastened  its  demise,  exterminating  the  bison  in  Maryland 
by  1775.  The  Glades  Star  (publication  of  the  Garrett  County  Histori- 
cal Society)  for  1943,  says  that  around  1774  one  of  the  Ashbys  (early 
settlers  in  the  Glades  of  Garrett  County)  and  a  neighbor  were  search- 
ing for  the  neighbor's  cows  one  day  in  early  winter.  They  followed 
the  tracks  of  some  animals  in  the  light  snow  until  they  came  to  what 
is  now  the  J.  J.  Ashby  farm,  when  Ashby  saw  a  bunch  of  wooly  hair 
on  a  snag.  Following  the  trail  still  farther  to  the  hill  southeast  of  the 
present  town  of  Grellin,  they  spotted  4  bison.  They  shot  the  bulls 
and  the  cows  escaped  westward.  These  were  the  last  seen  in  the  Glades, 
and  probably  the  last  of  Maryland's  bison  herd. 

The  former  occurrence  of  the  bison  is  still  indicated  by  such  place 
names  as:  Buffalo  Road  (Carroll  and  Frederick  Counties)  ;  Buffalo 
Run,  Little  Buffalo  Run,  and  Buffalo  Marsh  (Garrett  County). 

Mansueti  (1950)  lists  2  additional  species  (fisher,  Maries  pennanti; 
and  Canada  lynx.  Lynx  canadensis)  that  may  have  occurred  in  Mary- 
land in  the  past  but  are  not  presently  a  part  of  the  fauna  of  the  State. 
There  is  no  good  evidence,  however,  that  either  of  these  species  ever 
ranged  as  far  south  as  Maryland. 


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1951.  American  weasels.  University  Kansas  Publications,  Museum  Natural 
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1953.  Common  skunk  has  meal  of  yellow  jackets.  Maryland  Naturalist,  23 :  80. 
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1955.  Seminole  bat,  Lasiurus  seminolus,  in  central  New  York.  Journal  of  Mam- 
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1937.  Otter  caught  in  gill  net.  Maryland  Conservationist,  14 :  15.  Summer  Issue. 

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1940.  Mammals  of  Amelia  County,  Virginia.  Journal  of  Mammalogy,  21 :  422- 
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1951.  Notes  on  the  river  otter  (Lutra  canadensis) .  Journal  of  Mammalogy,  32: 
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1941.  Trouessart's  little  brown  bat  around  Baltimore.  Bulletin  Natural  History 
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1953.  The  varying  hare,  or  snowshoe  rabbit,  in  Maryland.  Maryland  Naturalist, 
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1961.  Kogia  stranded  in  Maryland.  Journal  of  Mammalogy,  42 :  26^270.  May. 
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1951.  American  wildlife  and  plants.  McGraw-Hill  Book  Co.,  New  York.  500  p. 
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1945.  Some  extinct  wild  animals  of  Tidewater.  Maryland  Tidewater.  News,  2 : 

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1952.  A  survey  of  West  Virginia  mammals.  Conservation  Commission,  West 
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1934.  Eastern  extension  of  the  range  of  Peromyscus  maniculatua  hairdii.  Jour- 
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1938.  The  ijairie  white-footed  mouse  in  New  York  State.  Journal  of  Mammalogy, 
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OCCIDENTAL  COLLEGE  LIBRARY 

1 49.30:66  docus 

Mammals  of  Maryland,  /Paradise, 


3  5043  00329  2652 


DATE  DUE 


Demco,  Inc.  38-293 


As  the  Nation's  principal  conservation  agency,  the  Department  of  the  Interior 
has  basic  resfwnsibilities  for  water,  fish,  wildlife,  mineral,  land,  park,  and  recre- 
ational resources.  Indian  and  Territorial  affairs  are  other  major  concerns  of  this 
department  of  natural  resources. 

The  Department  works  to  assure  the  wisest  choice  in  managing  all  our  re- 
sources so  that  each  shall  make  its  full  contribution  to  a  better  United  States 
now  and  in  the  future.