Skip to main content

Full text of "The condition and trend of aspen communities on BLM administered lands in north-central Nevada with recommendations for management : final report"

See other formats


8807049 


THE  CONDITION  AND  TREND  OF  ASPEN 
ON  BLM  LANDS  IN  NORTH-CENTRAL  NEVADA  - - 
WITH  RECOMMENDATIONS  FOR  MANAGEMENT 

YEAR  THREE 


Final 


report 

to 


Elko  Field  Office 
Bureau  of  Land  Management 
3900  Idaho  Street 
Elko,  NV  89801 


by 


Charles  E.  Kay,  Ph.D.  Wildlife  Ecology 
Wildlife  Management  Services 
480  East  125  North 
Providence,  UT  84332 
(435)  753-0715 


May  2003 

SD 
397 
. A7 
K394 
2003 
c . 2 


i%33 


ACKNOWLEDGEMENTS 


This  research  was  funded  by  the  Bureau  of  Land  Management  (BLM)  under 
Contract  Number  FBP  020036  and  I thank  the  agency  for  its  support.  BLM  specialists 
Skip  Ritter,  District  Forester,  and  Ken  Wilkinson,  Wildlife  Biologist,  were  extremely  helpful 
in  selecting  study  sites  and  providing  documents  germane  to  this  study.  This  report  is  part 
of  a continuing  5 year  aspen  study  (2000-2004)  between  the  Battle  Mountain  and  Elko 
BLM  Districts  funded  through  the  5900  Forest  Health  and  Restoration  Program.  Joe 
Ratliff,  Project  Coordinator  with  the  Battle  Mountain  Field  Office,  and  Skip  Ritter,  Project 
Coordinator  with  the  Elko  Field  Office,  express  their  appreciation  to  Rick  Tholen,  5900 
Project  Lead,  for  his  valued  support  and  assistance  in  making  this  project  possible. 


BLM  Library 
Denver  Federal  Center 
Bldg.  50,  OC-521 
P.O.  Box  25047 
Denver,  CO  80225 


TABLE  OF  CONTENTS 


ACKNOWLEDGEMENTS 

TABLE  OF  CONTENTS i 

LIST  OF  TABLES il 

LIST  OF  FIGURES iv 

ABSTRACT vii 

INTRODUCTION  AND  STUDY  AREA 1 

METHODS 7 

RESULTS  AND  SITE  ANALYSES 10 

Stag  Mountain 10 

Tuscarora  Mountains 69 

Adobe  Mountains  81 

DISCUSSION  AND  CONCLUSIONS 102 

MANAGEMENT  RECOMMENDATIONS „ 108 

LITERATURE  CITED 114 

APPENDIX  A - - Project  Maps 
APPENDIX  B - - Project  Data  Sheets 
APPENDIX  C - - Project  Color  Slides 


ttl 

LIST  OF  TABLES 

Table  Page 

1.  Aspen  stand  parameters  on  the  Deeth  Allotment,  Connors  Basin  Field 12 

2.  Age  and  diameter  of  aspen  on  the  Deeth  Allotment,  Connors  Basin  Field 15 

3.  Height  of  browsed  and  unbrowsed  aspen  suckers  in  recently  burned  aspen  stands  on 

the  Deeth  and  Stag  Mountain  Allotments 16 

4.  Understory  species  composition  of  aspen  stands  on  the  Deeth  Allotment,  Connors 

Basin  Field 17 

5.  Aspen  stand  parameters  on  the  Deeth  Allotment,  Hanks  Creek  Basin  Field 26 

6.  Age  and  diameter  of  aspen  on  the  Deeth  Allotment,  Hanks  Creek  Basin  Field 27 

7.  Understory  species  composition  of  aspen  stands  on  the  Deeth  Allotment,  Hanks  Creek 

Basin  Field 28 

8.  Aspen  stand  parameters  on  the  Stag  Mountain  Allotment,  McIntyre  Field 35 

9.  Age  and  diameter  of  aspen  on  the  Stag  Mountain  Allotment,  McIntyre  Field 37 

10.  Understory  species  composition  of  aspen  stands  on  the  Stag  Mountain  Allotment, 

McIntyre  Field 38 

11.  Aspen  stand  parameters  in  the  Tuscarora  Mountains 70 

12.  Age  and  diameter  of  aspen  in  the  Tuscarora  Mountains 71 

13.  Understory  species  composition  of  aspen  stands  in  the  Tuscarora  Mountains 72 

14.  Aspen  stand  parameters  in  the  Adobe  Mountains 82 

15.  Age  and  diameter  of  aspen  in  the  Adobe  Mountains 84 

16.  Understory  species  composition  of  aspen  stands  in  the  Adobe  Mountains 85 


w 


LIST  OF  FIGURES 

Figure  Page 

1.  General  location  of  aspen  study  sites  in  north-central  Nevada 6 

2.  Unburned  aspen  stand  EK-214  in  the  Connors  Basin  Field,  Deeth  Allotment 20 

3.  Unbumed  aspen  stand  EK-227  in  the  Connors  Basin  Field,  Deeth  Allotment 21 

4.  Burned  aspen  stand  EK-232  in  the  Connors  Basin  Field,  Deeth  Allotment 22 

5.  Aspen  stand  EK-217  in  the  Connors  Basin  Field,  Deeth  Allotment 23 

6.  Aspen  stand  EK-228  in  the  Connors  Basin  Field,  Deeth  Allotment 24 

7.  Aspen  stand  EK-209  inside  the  East  Hanks  Creek  Exclosure,  Hanks  Creek  Basin 

Field,  Deeth  Allotment 29 

8.  Aspen  stand  EK-21 1 inside  the  Antelope  Basin  Exclosure,  Hanks  Creek  Basin  Field, 

Deeth  Allotment 30 

9.  Aspen  sucker  inside  the  West  Hanks  Creek  Exclosure,  Hanks  Creek  Basin  Field, 

Deeth  Allotment 31 

10.  Aspen  stand  EK-21 2 outside  the  Antelope  Basin  Exclosure,  Hanks  Creek  Basin  Field, 

Deeth  Allotment 32 

11.  Aspen  stand  EK-240,  McIntyre  Field,  Stag  Mountain  Allotment 40 

12.  Aspen  stand  EK-247,  McIntyre  Field,  Stag  Mountain  Allotment 41 

13.  Aspen  stand  EK-249,  McIntyre  Field,  Stag  Mountain  Allotment 42 

14.  Aspen  stand  EK-251 , McIntyre  Field,  Stag  Mountain  Allotment 43 

15.  Aspen  stand  EK-239  viewed  northwest,  McIntyre  Field,  Stag  Mountain  Allotment 44 

16.  Aspen  stand  EK-239  viewed  northeast,  McIntyre  Field,  Stag  Mountain  Allotment 45 


17.  Fenceline  contrast,  Cheveller  Exclosure,  McIntyre  Field,  Stag  Mountain  Allotment.. ..47 

18.  Aspen  stand  EK-241  inside  the  Cheveller  Exclosure,  McIntyre  Field,  Stag  Mountain 


Allotment 48 

19.  Browsed  aspen  sucker  inside  the  Cheveller  Exclosure 49 


V 


20.  A recent  beaver  dam  inside  the  Cheveller  Exclosure 50 

21.  Aspen  stand  EK-242  inside  the  Cheveller  Exclosure 51 

22.  Aspen  stand  EK-243  inside  the  Cheveller  Exclosure 52 

23.  Recent  beaver  activity  on  an  unnamed  tributary  to  the  South  Fork  of  Hanks  Creek, 

Connors  Basin  Field,  Deeth  Allotment 54 

24.  Old  beaver  activity  on  an  unnamed  tributary  to  the  South  Fork  of  Hanks  Creek, 

Connors  Basin  Field,  Deeth  Allotment 55 

25.  Old  beaver  activity  on  Connors  Creek,  Connors  Basin  Field,  Deeth  Allotment 56 

26.  Old  beaver  activity  on  upper  Cottonwood  Creek,  McIntyre  Field,  Stag  Mountain 

Allotment 57 

27.  Allotment  boundary  comparison 59 

28.  Aspen  stand  EK-234,  Connors  Basin  Field,  Deeth  Allotment 60 

29.  Aspen  stand  EK-233,  McIntyre  Field,  Stag  Mountain  Allotment 61 

30.  Aspen  stand  EK-234,  Connors  Basin  Field,  Deeth  Allotment 62 

31.  Aspen  along  an  unnamed  tributary  to  Pole  Creek,  Indian  Creek  Field,  Devils  Gate 

Allotment 64 

32.  Aspen  along  Pole  Creek  on  the  Pole  Creek  Allotment 66 

33.  Close  up  of  a burned  aspen  stand  along  Pole  Creek 67 

34.  An  old  beaver  dam  on  Pole  Creek,  Pole  Creek  Allotment 68 

35.  A typical  aspen  stand  along  Nelson  Creek 73 

36.  Typical  aspen  stands  along  Lewis  Creek 74 

37.  Aspen  in  upper  Toe  Jam  Creek 75 

38.  Close  up  of  aspen  in  upper  Toe  Jam  Creek 76 

39.  Aspen  stand  EK-253  in  upper  Toe  Jam  Creek 77 

40.  Aspen  in  upper  Rock  Creek 78 

41 . Aspen  in  upper  Big  Cottonwood  Canyon 79 


VI 


42.  Close  up  of  a heavily  grazed  aspen  stand  along  upper  Dry  Creek  in  the  Tuscarora 

Mountains 80 

43.  Aspen  stand  EK-264  in  the  Adobe  Mountains 87 

44.  Close  up  aspen  stand  EK-264  in  the  Adobe  Mountains 88 

45.  Aspen  stand  EK-270  in  the  Adobe  Mountains 89 

46.  Aspen  stand  EK-272  in  the  Adobe  Mountains 90 

47.  A de  facto  exclosure  in  aspen  stand  EK-272  in  the  Adobe  Mountains 91 

48.  Aspen  inside  Long  Canyon  Exclosure  number  one 92 

49.  Close  up  of  aspen  inside  Long  Canyon  Exclosure  number  one 93 

50.  Aspen  inside  Coal  Mine  Canyon  Exclosure  number  two 94 

51.  Aspen  inside  Coal  Mine  Canyon  Exclosure  number  three 95 

52.  Typical  riparian  conditions  in  the  Adobe  Mountains 96 

53.  Fenceline  contrast  at  Coal  Mine  Canyon  Exclosure  number  one 97 

54.  Ungrazed  riparian  area  inside  Coal  Mine  Canyon  Exclosure  number  one 98 

55.  Grazed  riparian  area  below  Coal  Mine  Canyon  Exclosure  number  one 99 

56.  Soil  erosion  in  the  Adobe  Mountains 100 

57.  Close-up  of  sheet  erosion  in  Long  Canyon 101 


VII 


ABSTRACT 


Aspen  is  of  special  concern  in  the  West  because  the  species  does  not  commonly 
grow  from  seed  due  to  its  demanding  seed-bed  requirements.  It  is  thought  that 
environmental  conditions  have  not  been  conducive  to  seedling  growth  and  clonal 
establishment  since  shortly  after  the  glaciers  retreated  10,000  or  more  years  ago.  Hence, 
aspen  clones  found  in  north-central  Nevada  today  have  likely  maintained  their  presence 
on  those  sites  for  thousands  of  years  via  vegetative  regeneration;  i.e.  root  sprouting.  In 
addition,  aspen  communities  support  an  array  of  other  species  and  have  the  highest 
biodiversity  of  any  upland  forest  type  in  the  West.  This  is  especially  true  in  north-central 
Nevada  where  many  aspen  stands  are  associated  with  riparian  habitats.  Aspen,  though, 
has  been  declining  in  Nevada  and  throughout  the  Intermountain  West  since  shortly  after 
European  settlement.  The  reasons  for  this  have  been  attributed  to  climatic  change,  fire 
suppression,  normal  plant  succession,  wild  ungulate  browsing,  and/or  grazing  by  domestic 
livestock. 

To  test  these  hypotheses  and  to  determine  the  status  of  aspen  on  BLM 
administered  lands  in  north-central  Nevada,  I measured  75  representative  aspen  stands 
on  Stag  Mountain  and  in  the  Tuscarora  and  Adobe  Mountains.  I also  measured  all  aspen- 
containing  exclosures  in  those  areas.  The  exclosures  were  originally  built  to  study  the 
effect  of  livestock  use,  but  because  the  general  climate  is  the  same  inside  and  outside  the 
fenced  plots,  the  exclosures  can  also  be  used  to  evaluate  the  climatic  change  hypothesis. 
The  same  is  true  of  de  facto  exclosures  created  by  fallen  aspen  trees  or  other  physical 


barriers. 


VIII 


Many  aspen  stands  in  north-central  Nevada  have  not  produced  new  stems  greater 
than  6 feet  tall  in  nearly  100  years  and  many  stands  are  in  very  poor  condition.  The  status 
and  trend  of  aspen  communities  in  north-central  Nevada,  however,  is  not  related  to 
climatic  variation,  fire  suppression,  forest  succession,  or  browsing  by  mule  deer.  Instead, 
the  condition  of  individual  aspen  communities  is  related  to  past  and  present  levels  of 
livestock  grazing.  That  is,  aspen  is  declining  throughout  most  of  north-central  Nevada  due 
to  repeated  browsing  of  aspen  suckers  by  cattle  and/or  domestic  sheep  - - repeated 
browsing  eliminates  sucker  height  growth,  which  prevents  their  maturation  into  aspen 
saplings  and  trees.  Without  stem  replacement,  aspen  clones  are  consigned  to  extinction. 

This  cause  and  effect  relationship  is  most  clearly  demonstrated  inside  and  outside 
exclosures.  In  all  cases  where  it  was  protected,  aspen  successfully  regenerated  without 
fire  or  other  disturbance,  while  on  adjacent,  outside  plots,  aspen  continued  to  decline. 
Aspen  in  north-central  Nevada  also  experienced  major  regeneration  events  on  allotments 
where  livestock  use  was  reduced.  Fire  can  be  used  to  stimulate  aspen  regeneration,  but 
burned  aspen  stands  must  be  rested  for  several  years  until  the  majority  of  new  stems  are 
beyond  the  reach  of  livestock.  Beaver-felled  aspen  also  need  to  be  protected  or  repeated 
livestock  use  will  eliminate  those  clones,  as  has  already  happened  on  some  allotments. 

Thus,  to  reverse  the  decline  of  aspen  in  north-central  Nevada  it  will  be  necessary  to 
more  closely  manage  livestock.  Depending  on  individual  sites  and  the  present  condition  of 
aspen,  it  may  be  necessary  to  fence  some  stands  and/or  restrict  livestock  to  only  early- 
season  grazing.  If  aspen  does  not  respond  to  those  measures,  it  may  be  necessary  to 
reduce  AUM  numbers  on  some  allotments.  It  is  also  recommended  that  BLM  establish 


ix 


permanent  monitoring  plots  in  representative  aspen  communities  throughout  the  Elko 
District  to  evaluate  management  actions  related  to  that  species. 


1 


INTRODUCTION 


Aspen  (Populus  tremuloides)  is  an  excellent  indicator  of  ecosystem  health 
and  ecological  integrity  in  the  western  United  States  because  the  species  does  not 
commonly  grow  from  seed  due  to  its  demanding  seed-bed  requirements  (Perala 
1990;  West  et  al.  1994:10;  White  et  al.  1998a,  1998b).  In  fact,  there  are  no  known 
instances  of  aspen  clones  having  established  from  seed  anywhere  in  the 
Intermountain  West  during  the  period  of  recorded  history  (Kay  1 993).  It  is  thought 
that  environmental  conditions  have  not  been  conducive  to  seedling  growth  and 
clonal  establishment  since  shortly  after  the  glaciers  retreated  10,000  or  more  years 
ago  (McDonough  1979,  1985;  Perala  1990;  Jelinski  and  Cheliak  1992;  Mitton  and 
Grant  1 996).  This  means  that  aspen  clones  found  in  north-central  Nevada  today 
have  likely  maintained  their  presence  on  those  sites  for  thousands  of  years  via 
vegetative  regeneration.  Thus,  aspen  may  be  among  the  oldest  living  organisms 
on  Earth  and  should  be  managed  as  old-growth,  ancient  forests,  not  a serai  plant 
community  (Grant  1993;  Mitton  and  Grant  1996;  Kay  1997a,  2001a). 

Aspen  seedlings  are  more  common  in  the  northern  Canadian  Rockies 
(Peterson  and  Peterson  1992,  1995)  and  there  may  be  "windows  of  opportunity" 
that  allow  seedling  establishment  at  infrequent,  200  to  400  year  or  longer,  intervals 
(Jelinski  and  Cheliak  1992:728),  but  successful  sexual  reproduction  of  aspen  is  still 
exceedingly  rare  (Mitton  and  Grant  1996).  Aspen  invariably  occur  as  clones  in 
which  all  the  individual  trees  (ramets)  are  genetically  identical,  having  grown  from  a 
common  root  system  by  vegetative  shoots.  If  aspen  is  lost,  there  are  no  known 
means  of  reestablishing  those  clones  (Kay  1997a). 

As  a relatively  short-lived  tree  (<150  years),  long-lived  aspen  clones  are 
often  dependent  on  periodic  disturbance  such  as  fire  to  stimulate  vegetative 
regeneration  via  root  suckering,  and  to  reduce  conifer  competition  (Bartos  and 


2 


Mueggler  1979,  1981;  Bartos  et  al.  1991,  1994;  Shepperd  1993;  Shepperd  and 
Smith  1993).  In  the  absence  of  fire,  many  aspen  clones  in  the  Intermountain  West 
may  be  replaced  by  more  shade-tolerant  species,  although  climax  aspen  is 
common  (Mueggler  1988).  Aspen,  however,  will  bum  only  when  it  is  leafless  and 
when  the  understory  plants  are  dry  enough  to  carry  a fire,  conditions  that  occur  only 
early  in  the  spring  before  understory  regrowth,  and  late  in  the  autumn  after  leaf-fail 
and  the  understory  plants  have  cured  (Fechner  and  Barrows  1976,  Brown  and 
Simmerman  1986,  DeByle  et  al.  1987).  During  both  those  periods,  though,  there 
are  few  lightning  strikes  and  virtually  no  lightning-started  fires  in  the  West  (Kay 
1997a,  2000).  This  would  suggest  that  in  pre-Columbian  times,  native  burning  may 
have  been  more  important  than  lightning-started  fires  in  maintaining  aspen  and 
other  plant  communities  (Kay  1997a,  1997b,  1997c,  2000).  In  central  Nevada, 
though,  most  aspen  stands  are  relatively  small  and  recent  wildfires  burning  under 
extreme  conditions  have  completely  top-killed  some  clones;  i.e.,  wind-driven 
wildfires  are  able  to  burn  through  drought-stricken  aspen  if  the  stands  are  not  too 
large  or  if  the  clones  are  highly  degraded. 

In  addition,  aspen  communities  support  an  array  of  other  species  and  have 
extremely  high  biological  diversity  (DeByle  and  Winokur  1985,  Peterson  and 
Peterson  1992,  Stelfox  1995).  In  fact,  aspen  has  the  highest  biodiversity  of  any 
upland  forest  type  in  the  West  (Finch  and  Ruggiero  1993).  Bird  communities,  for 
instance,  vary  with  the  size,  age,  and  location  of  aspen  clones,  as  well  as  with 
grazing  intensity  and  history  (Young  1973,  1977;  Baida  1975;  Flack  1976,  Page  et 
al.  1978;  Wnternitz  1980;  Casey  and  Hein  1983;  Oakleafet  al.  1983;  Taylor  1986; 
Putman  et  al.  1989;  Daily  et  al.  1993;  Ehrlich  and  Daily  1993;  Johns  1993; 
Westworth  and  Telfer  1993;  Stelfox  1995;  Grant  and  Berkey  1999).  So  if  aspen  is 
lost,  many  birds  and  small  mammals  will  decline;  some  precipitously  (Ehrlich  and 
Daily  1993).  This  is  especially  true  on  BLM  lands  in  north-central  Nevada  where 


many  aspen  communities  are  found  in  riparian  settings  (Schenbeck  and  Dahlem 
1977,  Kennedy  et  al.  2000,  Kay  2001a). 


3 


Moreover,  aspen  provides  highly  palatable  forage  for  elk  (Cervus  elaphus), 
mule  deer  (Odocoileus  hemionous).  and  livestock  throughout  the  West  (Wallmo 
and  Regelin  1981,  Nelson  and  Leege  1982,  Endersby  1999).  Aspen,  however,  is 
sensitive  to  repeated  browsing  and  range-use  levels.  High-density  elk  populations 
commonly  strip  bark  from  mature  aspen  and  severely  browse  aspen  suckers  that 
can  prevent  stand  regeneration  and  which  may  eventually  lead  to  the  loss  of  aspen 
clones  (Krebill  1972;  Olmsted  1977,  1979,  1997;  Weinstein  1979;  Kay  1985,  1990, 
2001b,  2001c;  Shepperd  and  Fairweather  1994;  Baker  et  al.  1997;  White  et  al. 
1998a,  1998b;  Ripple  and  Larson  2000;  White  2001).  Large  numbers  of  mule  deer 
can  also  prevent  aspen  regeneration  (Olmstead  1979,  Kay  and  Bartos  2000),  and  if 
not  properly  managed,  livestock  can  have  similar  negative  impacts  on  aspen 
communities  (Baker  1918,  1925;  Sampson  1919;  Coles  1965;  Weatherill  and  Keith 
1969;  Kay  2001  a,  2002). 

Recent  evidence  indicates  that  aspen  has  been  declining  throughout  the 
Intermountain  West  since  shortly  after  European  settlement  (Schier  1975;  Schier 
and  Campbell  1980;  Kay  1997a,  1997b).  Since  1962,  the  acreage  of  aspen 
dominated  forests  in  Arizona  and  New  Mexico  has  decreased  by  nearly  50%  (U  S. 
Forest  Service  1993,  Cartwright  and  Burns  1994,  Johnson  1994).  While  in  the 
northern  Rockies,  aspen  has  declined  by  up  to  90%  since  the  late  1800s  (Kay 
1990,  1997a,  1997c;  Kay  and  Wagner  1994,  1996;  Kayetal.  1999).  On  Idaho’s 
Targhee  National  Forest,  inventory  data  show  that  36%  of  the  West  Camas  Creek 
drainage  was  dominated  by  aspen  in  1914,  but  today,  aspen  occupies  only  4%  of 
the  area  - - figures  that  are  confirmed  by  repeat-photographs  (Kay  1997a,  1999).  In 
Utah,  aspen  has  also  declined  from  its  historical  distribution  (Bartos  and  Campbell 
1998).  On  Utah’s  Dixie  National  Forest,  for  instance,  there  were  historically  over 


4 


590,000  A.  of  aspen  while  today  there  are  only  approximately  200,000  A. 
Furthermore,  many  aspen  stands  contain  old-age  or  single-age  trees  and  have  not 
successfully  regenerated  for  80  years  or  longer  (Mueggler  1 989a,  1 989b).  It  has 
also  been  observed  that  aspen  has  failed  to  regenerate  and  is  declining  on  BLM 
lands  in  central  Nevada  (Schenbeck  and  Dahlem  1977). 

At  least  four  hypotheses  have  been  advanced  to  explain  the  decline  of 
aspen  throughout  the  Intermountain  West  (Kay  and  Bartos  2000,  White  et  al. 

2003).  (1 ) Climatic  change  - - the  climate  was  more  favorable  for  aspen  in  the  past 
and  today’s  drier  climate  precludes  aspen  regeneration  (Despain  et  al.  1986, 
Romme  et  al.  1995,  Baker  et  al.  1997).  (2)  Conifer  invasion  and  fire  suppression  - - 
aspen  is  a serai  species  that  will  not  successfully  regenerate  unless  the  overstory 
aspen  and  invading  conifers  are  killed  by  fire  (Houston  1973,  1982;  Loope  and 
Gruell  1973;  Gruell  and  Loope  1974;  Despain  et  al.  1986),  and  thus,  modern  fire 
suppression  and  forest  succession  have  adversely  effected  aspen.  (3)  Livestock 
grazing  is  preventing  the  growth  of  aspen  suckers  into  trees  (Sampson  1919,  Baker 
1925).  And  (4)  repeated  browsing  by  mule  deer  and/or  elk  is  preventing  aspen 
sucker  height  growth  and  the  successful  regeneration  of  aspen  stands  (Coles  1965; 
Bartos  and  Mueggler  1979,  1981). 

To  test  these  hypotheses  and  to  determine  the  status  of  aspen  on  BLM 
lands,  I measured  the  condition  and  trend  of  aspen  communities  throughout  north- 
central  Nevada  within  the  Elko  District  (Figure  1 ) - - similar  to  my  work  for  the  Battle 
Mountain  and  Elko  Districts  in  2000  and  2001  (Kay  2001a,  2002).  As  before,  I also 
measured  all  aspen-containing  exclosures  within  the  study  areas.  These 
exclosures  were  originally  built  to  study  the  effect  of  livestock  use,  but  because  the 
general  climate  is  the  same  inside  and  outside  the  fenced  plots,  they  can  also  be 
used  to  test  the  climatic  change  hypothesis  (Laycock  1975).  Stag  Mountain  and 
the  Tuscarora  and  Adobe  Mountains  were  selected  for  study  by  the  Bureau  of  Land 


5 


Management  because  aspen  stands  in  those  areas  are  thought  to  be 
representative  of  conditions  on  the  Elko  District. 


6 


(arson 


OWYHEE 


TWIN 


Jnckpot 

El  5265/ 


Owyhee 


HUMBOU>T  1 — I | 

Merrill  Min  v 

, aEI  B78&  p Jttrbic 

^Mountain  City  KAf^OKAL 
/ Copper  Mtn  \ 

V 27  * 


[Charlaftli 


f H V Shfhmil 
K)  El  62? j 


Pequop  buineRtf 
F'  6067 


Death 


Spring  -/j- 
Crook  r 

v^2i7f^’l.nmoille 


Emigrant i 
Pats' 

El  6H4 


Wendover 
Air  Force 
Auxiliary  Field 


'Carlin 

El  4959 


rJ35\a 
*»Ot 
^ Ruby 
7\  Mtn 
. 1 Scenic 
Areal 
ItATLA 


\C0ShulV 
Peat i 
-F(  9610 


South  For* 
Indian 
Reaervatlon 
7h 

In 

Rooms  on  Min 
’A  El  81 12 


ip  rue  v Min 
: I W2& 


Franklin 

l.riK’’  <o 


South  Fork 

Indian 

Reaervatior 


Pearl 

Peak! 


[Corfu* 


Ruby  Lake 
National 
Wildlife  Refuge 


Railroad  Past 
El  5896 


ShontytQwnfV  1 7 


Duck 


PALLS 


Valley 


Indian 


Hal  Pa  a* 


Gollahar  Mm 


El  6025 


El  B 1 53 


i 


Reservation  1225 


z 


While  Roc A 
Min 
El  7604 


Middlu  Slack 
Min  / 


B.rti 

nl  (•  Puttk 


El  8W4 


Whiti 


(•Ho] 


El  9288  ' 


Chine  Mi 
El  8350 


I 


Delano  Peak 

El  7847 


K. 


Chicken  Creek  *\^ 
Summit  Ei  6441 

JacK  Cfookl 

(226 

McCann  Creek  Min 
_ El  860. 


O Qe.iAf  Peak  ? 

* -Ettafli  w 

g > §1 


* Pilot  Peak 

1 ’ El  10715 


1 1 

:'/jfr  Zone » 


i LhovIHh 


O ' (sue 


C» 


* 

Afr  Lawn 
Ei  9680 , 


- 


'•f-  C'tr  .con' 


Vaiiny 


trr* 


^ While  He 

x «o  Past 


Isilei 


FV 


£ Geld  Acre 

z*  (sue  • 


60* 


Mt  lanaoo 
tl  9162 


J4 


Eiaphanl  He  no 
Ei  8405 


Cone: 


< /- 

WT1  %. 


Logos  Stniiorr 


Bntd  Mm 
Ei  855 3 


Goahi 


Cki  Peal 


Figure  1 General  location  of  aspen  study  sites  in  north-central  Nevada  1 - - Stag 
Mountain;  2 - - Tuscarora  Mountains;  and  3 - - Adobe  Mountains. 


7 


METHODS 

Within  each  study  area,  representative  aspen  stands  were  selected  for 
detailed  measurement.  At  each  aspen  community  that  was  sampled  during  this 
study,  I first  placed  a 2x30  m (6.6x98  ft.)  belt  transect  perpendicular  to  the  slope  in 
the  stand's  center.  To  facilitate  data  recording,  I subdivided  each  30  m transect  into 
3 m (9.8  ft.)  segments  and  then  recorded  the  number  of  live  aspen  stems  by  size 
classes  within  each  3 m segment.  I used  the  following  size  classes:  (1)  stems  less 
than  2 m (6.6  ft.)  tall,  (2)  stems  greater  than  2 m tall  but  less  than  5 cm  (2  in.) 
diameter  at  breast  height  (DBH),  (3)  stems  between  6 and  10  cm  (2-4  in.)  DBH,  (4) 
stems  between  1 1 and  20  cm  (4-8  in.)  DBH,  and  (5)  stems  greater  than  21  cm  (8 
in.)  DBH.  Ages  of  aspen  within  each  size  class  were  determined  by  counting 
annual  rings.  I obtained  the  ages  of  large  aspen  with  the  aid  of  an  increment  borer 
while  I cross-sectioned  smaller  stems,  usually  those  less  than  5 cm  DBH.  Larger 
trees  were  cored  at  breast  height,  while  stems  <5  cm  in  diameter  were  usually  cut 
at  ground  level.  Stems  less  than  2 m tall  were  not  aged.  The  location  of  each 
measured  aspen  stand  was  plotted  on  1 :24,000  USGS  topographic  maps.  In 
addition,  the  locations  of  all  aspen  stands  within  each  study  area  were  also  marked 
on  topographic  maps,  as  were  all  the  routes  driven  or  walked. 

Wthin  each  stand,  I also  recorded  the  following  information:  (1)  location  - - 
section,  township,  and  range;  (2)  elevation  as  determined  from  topographic  maps; 
(3)  Universal  Transverse  Mercator  (UTM)  grid  coordinates,  again  estimated  from 
topographic  maps;  (4)  aspect  - north,  northeast,  east,  southeast,  south,  southwest, 
west,  and  northwest;  (5)  estimated  slope  in  percent;  (6)  estimated  stand  size;  (7)  an 
estimate  of  the  mean  percent  of  each  stem  that  had  been  damaged  by  ungulate 
bark  stripping  - - of  the  animals  commonly  found  in  Nevada,  bark  stripping  is  only 
done  by  elk,  not  deer  or  livestock  (Krebill  1972);  (8)  if  the  stand  had  newly 


8 


regenerated  stems  greater  than  2 m tall  but  less  than  5 cm  DBH,  an  estimate  of  the 
percent  that  showed  evidence  of  ungulate  highlining  - - where  the  ungulates  browse 
off  all  the  lower  branches  as  high  as  the  animals  can  reach;  (9)  the  percent  of 
stems  less  than  2 m tall  on  each  2x30  m transect  that  exhibited  ungulate  browsing; 
(10)  whether  or  not  water  was  present  in  or  near  the  stand;  and  (1 1 ) the  number  of 
cattle,  domestic  sheep,  mule  deer,  and  elk  pellet  groups  on  each  2x30  m belt 
transect.  At  recently  burned  stands,  I also  measured  the  height  of  50  randomly 
chosen  aspen  suckers  and  recorded  whether  those  stems  had  been  browsed  or 
not. 

Furthermore,  at  each  stand  I recorded  the  number  and  species  of  conifers 
on  the  2x30  m belt  transect  that  was  used  to  count  aspen  stems.  Conifers  were 
recorded  by  the  same  five  size  classes  that  were  used  for  aspen.  In  addition,  I 
estimated  the  total  percent  conifer  canopy  cover  in  each  stand  according  to 
guidelines  established  by  Mueggler  (1988).  Understory  plant  species  composition 
was  visually  estimated  in  each  sampled  aspen  stand  following  procedures 
developed  by  Mueggler  (1988).  Shrubs  were  identified  to  species,  but  the  same 
could  not  be  done  with  grasses  or  forbs  because  those  plants  had  generally 
received  such  heavy  utilization  that  they  could  not  reliably  be  identified  (Clary  and 
Leininger  2000;  Kay  2001a,  2002).  Instead,  percent  canopy  cover  was  estimated 
for  all  grass  species  and  all  forb  species  combined.  The  proportion  of  bare  soil, 
rock,  and  litter,  including  downed  aspen,  was  also  recorded.  All  aspen  selected  for 
detailed  study  were  photographed  using  35  mm  color  slide  film  to  document  stand 
and  understory  conditions  (Magill  1989;  Hall  2002a,  2002b).  Finally,  at  each  aspen- 
containing  exclosure,  data  were  collected  on  inside,  as  well  as  on  adjacent, 
comparable  outside  plots  (Kay  and  Bartos  2000). 

BLM  provided  information  on  the  grazing  history  of  each  aspen  study  area. 
Unfortunately,  the  agency’s  files  are  incomplete  and  seldom  contain  data  on  actual 


9 


livestock  use.  Instead,  BLM  generally  has  information  on  AUM  (Animal  Unit 
Month)  allocations,  as  well  as  the  number  of  AUMs  each  permittee  paid  to  activate 
in  any  one  year,  called  grazing  bills.  Grazing  bills,  however,  may  not  reflect  actual 
use  as  many  ranches  simply  pay  for  all  the  AUMs  they  are  allocated  each  year  to 
maintain  their  grazing  permits.  At  the  end  of  each  grazing  season,  ranchers  are 
required  to  submit  actual  use  reports,  but  those  too  are  only  estimates.  Therefore, 
based  on  the  information  in  BLM’s  files,  it  is  only  possible  to  document  general 
grazing  trends  on  each  allotment.  BLM,  for  instance,  does  have  records  on  legally 
mandated  changes  in  AUM  allocations.  That  is  to  say,  have  the  ranchers’  basic 
AUM  authorizations  been  increased  or  decreased?  BLM  also  has  data  on  any 
season-of-use  changes  that  have  been  implemented  by  the  agency.  Again, 
however,  actual  use  data  are  lacking  because  there  simply  are  not  enough  agency 
personnel  to  field  check  each  and  every  action  of  its  grazing  permittees. 


10 


RESULTS  AND  SITE  ANALYSES 

In  all,  75  representative  aspen  stands  were  measured  on  Stag  Mountain 
and  in  the  Tuscarora  and  Adobe  Mountains.  The  stands  were  numbered 
consecutively  from  EK-201  to  EK-275  as  they  were  measured  in  the  field. 
Appendix  A contains  the  1:24,000  project  maps,  while  copies  of  the  original  data 
sheets  are  located  in  Appendix  B.  Appendix  C contains  1 ,056  - - 35  mm  color 
slides  of  project  aspen  stands.  No  instances  of  ungulate  bark  stripping  were 
recorded  during  this  study,  so  those  data  were  omitted  from  the  summary  tables 
for  each  study  area.  Conifers  were  absent  from  all  aspen  stands,  so  those  data 
were  also  omitted  from  the  tabular  summaries,  but  may  be  found  on  the  original 
data  sheets  (Appendix  B). 


Stag  Mountain 

The  study  area  on  Stag  Mountain  included  four  allotments  - - 
Deeth,  Stag  Mountain,  Devils  Gate,  and  Pole  Creek.  The  Deeth  Allotment 
included  Connors  Basin  Field  and  Hanks  Creek  Basin  Field,  while  the  Stag 
Mountain  Allotment  included  McIntyre  Field  and  the  Cheveller  Exclosure,  per  the 
allotment  map  provided  by  BLM.  In  all,  52  aspen  stands  were  measured  (EK- 
201  to  EK-252;  see  Appendix  A)  and  those  data  are  presented  in  Tables  1 to  10, 
as  well  as  Appendix  C (slides  1-601). 


11 


Deeth  Allotment  - Connors  Basin  Field 

Most  aspen  in  this  pasture  experienced  a major  regeneration  event  during 
the  early  1980’s  when  the  previous  permittee  went  bankrupt  and  the  range  was 
destocked  for  at  least  four  years  (Tables  1 to  4;  Figures  2 and  3).  This  is  similar 
to  what  happen  on  Bates  Mountain  where  aspen  regenerated  when  that 
allotment  was  partially  destocked  due  to  permittee  bankruptcy  (Kay  2001a). 
Connors  Basin  Field,  however,  was  swept  by  wildfire  in  2001  and  many  aspen 
stands  were  burned.  Consequently,  this  part  of  the  Deeth  Allotment  was  closed 
to  cattle  grazing  in  2001,  although  some  trespass  use  did  occur.  Regeneration  of 
burned  aspen  stands  ranged  from  7,000  to  nearly  60,000  stems  per  acre  and 
averaged  just  over  30,000  (n=17)  - - see  Table  1 and  Figures  4 to  6.  Mean 
sucker  height  one  year  following  fire  ranged  from  25  to  56  inches  and  averaged 
39  inches  (n=17)  - - see  Table  3.  It  is  anticipated  that  this  pasture  will  be  rested 
until  most  of  the  new  aspen  suckers  are  beyond  the  reach  of  cattle.  This  likely 
will  require  two  or  three  additional  years  of  non-use. 


Table  1.  Aspen  stand  parameters  on  the  Deeth  Allotment,  Connors  Basin  Field. 


12 


a> 

.Q 

E 

3 


"D 

C 

TO 

w 


to 

t — 
CM 

i 

* 

LU 


un 

r~~ 

CNI 

i 

* 

LU 


■M- 

T- 

z 

UJ 

LU  Z 

o 

UJ 

in 

o 

x — 

X — 

o 

OO 

o o 

CO 

Is- 

CM 

■ 

* 

■M- 

m 

m m 

T—  T— 
T~ 

CO 

CO 

X 

o 

CM 

LU 

CO  oo 
to  in 

•M- 

CO 

CM 

z 

LU 

UJ  z 

o 

UJ 

O 

O 

T — 

x — 

o 

CO 

o o 

o 

z 

t — 

m 

CM 

i 

* 

UJ 

-'fr 

m 

o m 
m o 

■M"  T- 

co  oo 
co  m 

CO 

CD 

in 

S3 

o 

Is- 

■M- 

OO 

CO 

z 

UJ 

LU  Z 

o 

UJ 

o 

o 

o 

X — 

o 

oo 

o o 

•M- 

i — 

o 

CM 

i 

* 

UJ 

m 

in  o 
m cm 
o 

CO  OO 

CO 

CO 

i 

m 

CO 

X 

o 

-M" 

h- 

O 

(Nl 

i 

* 

LU 


(D 

O 

CM 

i 

* 

LU 


m 

o 

CM 

i 

* 

LU 


■M- 

O 

CM 

i 

* 

LU 


CO 

o 

CM 

i 

* 

LU 


CM 

O 

CM 

LU 


o 

CM 

I 

* 

LU 


CM 


O 

■M" 


CM 


O 


UJ 

UJ  Z 

o 

UJ 

o 

o 

oo 

o o 

CO 

z 

-f 

oo 

m 

o o 
o in 

t"- 

co 

in 

X — 

X 

i*  CM 

o 

CO  oo 

co  m 

O) 

-u- 

LU 

UJ  Z 

o 

z 

o 

o 

oo 

o o 

to 

co 

o 

in 

m in 
Is-  co 
CO  CO 

r — 
co 

o 

CM 

S3 

o 

CO  OO 

T— 

co  in 

T"" 

M Z LU 

^ O M 

-M-  in 


co  z LU 
CM  O 03 
•M-  in 


in 


in 


Z LU 
o oo 
M-  in 


Z LU 
O oo 
tj-  in 


C XT 
o O)  0J 

~ c Dl 
C i C 
0)  o CO 

co  h-  a: 


uj  z 

o o 
o o 

1-  CO 
CO  CD 

-<r  r~. 
co  in 

■M- 


UJ 

o 

o 

■M- 


Z 

o 

o 

CO 


CO  OO 

co  r'- 
co  m 

M" 

LU  Z 
O o 
o o 

CO  Tf 
CM  03 
CO  |"- 

<o  m 

LU  Z 
O O 

o o 
■*-  00 
CM  03 
co  r-~ 
to  in 


o 

m 

co 

co 


o 

CM 

oo 

co 


o 

CM 


o 

CM 


LU 

z 


LU 


o 

CO 


LU 

z 


LU 


o 

CM 


o 

CO 

X 

o 

m 


o 

m 

X 

o 

co 


o 

o 

X 

o 

I"- 


o 

-O' 

T — 

X 

o 

03 


< 

z 


< 

z 


< 

z 


< 

z 


to  m 
•o- 


z 

UJ 

UJ  Z 

o 

UJ 

o 

o 

o 

oo 

O O 

00 

^ — 

in 

o in 
m <j> 

N 

CD 

1 

o 

X 

co  o 
to  oo 
co  m 

•O' 


I- 

D 


c 

o 

*■£3 

co 

> 

03 

UJ 


to 

8. 

(/) 

< 


& 

o 

(0 


10 

T3 

03 

N 

"(/> 

TO 

C 

CO 

C/) 


03  C 

c — 

03  -C 
03  03 
03  £ 

a: 


(/> 

S 

O 

-Q 

£ 

03 

O 

3 

CO 


o o o o o 

r*» 

o 

-M" 


r^-  o o o o 


o o o 


o o o 


03 

co 

co 


cm  m in 
M-  CO  CM 
r — co  o 
r-  m 


r-'- 

CD 


O O O 


00 

CD 

03 

CO 


o o o o 


o o o 


I"-  o o o o 

CO 

oo 

co 

CM 


o o o 


m 

Is- 

o 

in 


■'t 

CM 

CM 

00 


o o o o 


o o o 


o o o o 


o o o 


in  o o o o 

CO 

CO 

CO 


o o o 


oo 

CO 

M- 

o 

■M- 


o o o o 


o o o 


z 

UJ 

UJ 

o 

o 

UJ 

m 

o 

< 

o 

03 

o 

oo 

o 

o 

M 

z 

CM 

z 

m 

Tj- 

m 

o 

m 

oo 

X — 

CM 

o 

03 

CO 

X 

m 

co 

r- 

o 

CM 

co 

m 

oo 

to 

z 

LU 

UJ 

Z 

o 

LU 

o 

o 

< 

o 

03 

X — 

o 

oo 

o 

o 

o 

z 

o 

z 

03 

T}- 

m 

in 

m 

oo 

in 

CO 

M 

co 

CO 

X 

co 

CO 

o 

o 

M- 

CO 

oo 

oo 

o o o o 


o o o 


o o o o 


o o o 


CM 

CM 

03 

I''-’ 

CO 


o o o o 


o o o 


03 

l_ 

o 

3- 

V) 

0) 

■E 

</3 

c 

03 

■a  . 
E c 

® V 

CO 


X 

CD 

Q 

,E  I I T 

-ggg 

v .2  .2  d 

°?  OO 
CO  CM  Tf  A 


« 

(/) 

CL 

3 

5*  s & 

03  c 0) 

= m r 
03  o CO 
0. 


03 

03 

Q 


o 

z 


o 

z 


(/> 

03 

>- 


</> 

03 

>- 


10 

03 


(O 

03 

>- 


o 

z 


o 

z 


o 

z 


L 

03 

TO 

£ 


Pellet  groups  per  2x30  m (6.6  x 98  ft.)  belt  transect.  **Water  in  or  near  stand.  NA=Not  applicable. 


13 


2 

LL 


CA 

CO 

CQ 

£ 

o 

c 

c 

o 

O 

•4-^ 

c= 

<D 

E 

o 


cd 

a> 

Q 

a) 

.c 

c 

o 

e 

aj 

a> 

E 

CO 

t_ 

CO 

CL 

■a 

c 

TO 

to 

c 

a) 

CL 

CA 

< 


a> 

JO 

CO 


CD 

-Q 

E 

3 


■a 

c 

CO 

CO 


CO 

CM 

I 

LU 


CM 

CO 

CM 

i 

* 

LU 


CO 

CM 

i 

LU 


O 

CO 

CM 

■ 

LU 


CD 

CM 

CM 

i 

LU 


CO 

CM 

CM 

i 

LU 


I''- 

CM 

CM 

i 

* 

LU 


h~- 
^ — 
CM 

i 

* 

LU 


oo 

z 

LU 

LU  Z 

o 

LU 

o 

CM 

OO 

o o 

o 

z 

CO 

in 

o o 

O)  CM 

CD 

CO 

in 

CO 

CO 


LU 

oo 

to 


CO 


CO 

CO 


co  z LU 
CO  T-  oo 

Tfr  LD 


CO 


Z LU 
O oo 
M"  in 


Z LU 
O oo 
M"  m 


cr 

o 

T> 

a) 

CO 


T-  CD 

CO  oo 

co  in 


LU 

o 

o 

o 

CM 


z 

o 

m 

m 

M" 


O 

in 

o 

r-'- 


LU 


CO  oo 

co  in 


z 

LU 

LU 

Z 

o 

OO 

o 

o 

Tf 

in 

o 

o 

o> 

co 

CO 

CM 

M- 

CO 

OO 

CD 

in 

M- 

z 

LU 

LU 

z 

o 

00 

o 

o 

m 

o 

o 

o 

in 

OO 

1^- 

t — 

•M- 

CO 

oo 

CD 

in 

LU 


o 

CM 


m 


LU 


m 


LU  Z 
o o 
o o 
t—  r~- 
CM  M" 
CO  OO 

cd  in 

M- 


z 

o 

o 


LU 
o 
o 
o 

CM  CO 
CO  OO 

cd  m 


LU 
o 
o 
o 

CO 
CO  OO 

cd  m 

■M- 


o 

o 

CM 


o 

OO 

CD 

CD 


O 

OO 


O 

M- 

oo 

CD 


LU 

Z 


LU 


LU 


O 

CM 


O 


m 


o 

CD 

X 

o 


O 

00 

X 

o 

m 


o 

oo 

x 

o 

M" 


O 

O 

0O 

X 

o 

m 


o 

o 

CO 

X 

o 

o 

CM 


O 

CO 

X 

o 

n~ 


o 

oo 

T — 

X 

o 

o 


< 

Z 


< 

Z 


< 

z 


o o o o o 
o 

CD 

CD 


OO  o o o o 

CD 

h~ 

CO 

CO 


o o o o o 


o o o 


o 

z 


o o o 


o o 


o o o o o 


o o o 


OO  o o o o 

CD 

o 

CO 

CO 


T-  o o o o 

in 

CM 

o 


CD  T-  CO  O T- 

co  o oo  o 

CM  CM  CM  CM 

r-  co 


o o o 


o o o 


o o o 


T- 

Z 

LU 

LU 

z 

o 

LU 

o 

o 

O 

o 

in 

m 

in 

o 

O 

o 

o 

CM 

o 

00 

O 

o 

z 

CM 

o 

r-- 

co 

o 

CO 

CM 

in 

o 

o 

M- 

T“ 

co 

co 

o 

T— 

* 

LU 

CD 

o 

CO 

CM 

CM 

oo 

X 

o 

CD 

*" 

CD 

in 

■M- 

O 

o 

z 

UJ 

LU 

z 

o 

LU 

m 

O 

< 

< 

o 

o 

o 

o 

o 

O 

o 

o 

CM 

▼“ 

o 

oo 

o 

o 

oo 

z 

o 

z 

z 

CM 

i 

* 

LU 

in 

o 

oo 

co 

o 

CO 

oo 

CD 

CD 

3 

o 

m 

CD 

m 

T“ 

■M- 

CD 

o 

z 

LU 

in 

o 

o 

LU 

m 

o 

o 

o 

in 

M" 

oo 

h- 

O 

o 

o 

t — 

,T“ 

o 

oo 

CM 

o 

oo 

CM 

CD 

O 

o 

CO 

CO 

CM 

m 

oo 

o 

o 

in 

X 

co 

oo 

CO 

T — 

v> 

1 — 

^ — 

h- 

o 

CM 

X— 

X 

CO 

CO 

CO 

LU 

CD 

m 

M' 

oo 

o 

Z 

LU 

LU 

Z 

o 

UJ 

o 

o 

o 

o 

CM 

CD 

o 

oo 

O 

o 

o 

T— 

o 

oo 

o 

o 

CD 

z 

CO 

T“ 

r- 

o 

o 

CD 

CM 

i 

LU 

in 

o 

oo 

CO 

in 

n- 

o 

oo 

r~- 

1 

o 

2 

o 

CD 

o 

T— 

CM 

CM 

CM 

cd  in 

■O' 


z 

LU 

UJ  z 

o 

UJ 

o 

o 

oo 

O O 

CO 

M- 

in 

o o 
C"-  co 

CO 

N 

CD 

in 

co  oo 
cd  m 

M- 


o 

r- 

X 

o 

o 


T-  o o o o 

CD 


CD 

in 


o o o 


Q. 

c: 

E 

o 

CA  (D 

■5 

1 c 

2 

CO 

> 

(D 

Q_ 

O CCJ 

h- 

<D 

(A 

L—  CC 

D 

UJ 

< 

CD 

a. 

o 

(0 


(A 

"O 

>s 

CD 

N 

CA 

T3 

c 

co 

co 


2 s-' 

CD  C 
c — 

a> 

CD  CD 
CD  'E 

QL 


T3 

CD 

CA 

$ 

o 

L_ 

n 

£ 

CD 

o 

3 

co 


CD 

l_ 

o 

_C0 

CA 

CD 


X 

CQ 

a 


~ .E  x X 


CA 

c 

CD 

■a 

E c 

§ CO 
V 

co 


CM  g g CQ 


V 

v .E 
d m- 

CO  CM 


oo 


Q 


oo 

A 


* 

CA 

CL 

3 

o 


CL 
CD 
CD 

00(0 

CL 


cd  a) 

0)  ZP 
= co 


CD 

CD 

a 


CA 

(D 

> 


CA 

CD 


CA 

CD 


CA 

CD 

>- 


CA 

CD 


CA 

CD 

>- 


0) 

TO 


Pellet  groups  per  2x30  m (6.6  x 98  ft.)  belt  transect.  **Water  in  or  near  stand.  NA=Not  applicable. 


Table  1.  Aspen  stand  parameters  on  the  Deeth  Allotment,  Connors  Basin  Field. 


14 


CD 

-Q 


E 


TD 

C 

CD 


CO 


CO 

CO 

eg 

i 

* 

LU 


CM 


z 

UJ 

LU  Z 

o 

LU 

o 

00 

in 

o o 
o o 
CM  t- 

oo 

h» 

(O 

CO 

co  r-» 
co  oo 
m 


o 

o 

co 

x 

o 

o 


oo  o o o o 


o 

CO 


o o o 


(/> 

CD 


c -c: 

O CD 

~ c cn 
t)  i C 
CD  O TO 

co  i-  a: 


c 

o 

-4—* 

CD 

> 

0) 

LU 


ts 

| 

c/1 

< 


>P 

o' 

CD 

CL 

O 

CO 


co 

T3 

>, 

CD 

N 

V) 

T3 

C 

CD 

CO 


VO 


E 3 

CD  C 

S 2 
8*f 

a: 


-O 

CD 

C/> 

S 

O 


e 

CD 

O 

13 

CO 


CD 

i— 

o 

CD 

> — ■ 

C/1 

0) 

£ 

C/> 

c 

CD 

T3 

E 

CD 

CO 


X 

GO 

Q 


CM 

V 

V 

d 

CO  CM 


X X 
00  CO 
Q Q 


Tf  oo 


X 

CO 


oo 

A 


« 

c/1 

CL 

3 

O 


CD  d) 


CL 

CD  i- 
0)  JC  CD  CD 
= ra  r (D 

aiOCOO 

0. 


L 

a> 

TO 

£ 


Pellet  groups  per  2x30  m (6.6  x 98  ft.)  belt  transect.  **Water  in  or  near  stand.  NA=Not  applicable. 


15 


Table  2.  Age  and  diameter  of  aspen  on  the  Deeth  Allotment,  Connors  Basin  Field.  R=stem  with  heart  rot 
that  could  not  be  aged.  Burned=recently  burned  stand  in  which  all  the  overstory  trees  were  killed 
and  thus  no  age  data  recorded. 


Stand  Number 

Stem  Diameter  (inches)/Age  (yrs) 

EK-201 

Burned 

EK-202 

Burned 

EK-203 

Burned 

EK-204 

Burned 

EK-205 

Burned 

EK-205 

Burned 

EK-206 

Burned 

EK-207 

Burned 

EK-208 

Burned 

EK-213 

Burned 

EK-214 

4/20,  4/18,  4/19,  5/16,  5/18,  5/18,  5/20,  22/R 

EK-215 

Burned 

EK-216 

Burned 

EK-217 

Burned 

EK-218 

3/21,  3/20,  3/20,  3/20,  8/70,  9/71,  11/76 

EK-219 

1/10,  2/16,  2/17,  2/18,  2/18,  2/18,  3/17,  3/18,  8/50 

EK-220 

No  live  stems  in  stand 

EK-226 

1/8,  1/10,  2/15,  3/19,  3/18,  3/18,  3/18,  4/20,  14/96,  14/95,  17/R 

EK-227 

2/10,  2/18,  3/18,  3/20,  4/19,  4/20,  4/20,  5/20,  12/110,  12/110,17/108,  18/110,  20/115 

EK-228 

Burned 

EK-229 

Burned 

EK-230 

No  live  stems  in  stand 

EK-231 

No  live  stems  in  stand 

EK-232 

Burned 

EK-234 

Burned 

EK-236 

Burned 

Table  3.  Height  of  browsed  and  unbrowsed  aspen  suckers  in  recently  burned  aspen  stands  on  the  Deeth  and  Stag  Mountain  Allotments. 

All  stands  were  burned  in  2001  by  the  Stag  Mountain  fire.  EK-201  to  236  Deeth  Allotment.  EK-233  and  235  Stag  Mountain  Allotment. 


16 


■a 

co 


OO  05 

c\i  Tj-' 


-o 

<D 

</) 


£ 


O 


CO 


X 


c 


Tt  oo 
cri  co 


o o 

IT)  CO 


05 

<u 


I 


3 

X 


c 


COuScOCOa5CNCOcr)COCN't-;Ti;a)T-;CT>COCN4 
T-  •«-  T-  r-  T-  T-  CM  T-  1-  T-  T-  CM  T- 


M;  (O  CO  CO  ^ ® S M;  O N N S r;  r;  (J)  s 
(DOTfdnifi^oiNTtiricDTf^cooco 
COM-OCOCOCIM-COCO^OmCMM-COinM- 


ooooooooooooooooo 

LocncncoLococncocncocococncocncncn 


ooooooooooooooooo 


o 

o 


a> 

& 

E 

3 


■a 

c 

TO 

V) 


T-CMOM-lOCOh-OOCOincONOOCDCMM-CD 

OOOOOOOOt-t-1-t-CMCNICOCOCO 

CMCMCMCMCMCMCMCMCMCMCMCMCMCMCMCMCM 

• i i i i i i i i i i i i i i t i 

* :*:  *:  * * i sc:*:*:*:^:*:****:*:*: 
LUUJUJUJUJUJUJUJUJliJUJUJUJUJUJUJUJ 


co 

CO 

CM 

I 

* 

LU 


EK-235  100 


17 


m 

CM 

id 

LU 


m o 
CD 


■<* 

CM 

i 

LU 


m 


• in  h-  H 


co 

T 

CM 

i 

id 

LU 


m m 1 in  m 1 1 1 1 


oo 

o 

CM 

I 

* 

LU 


in  o 1 m 1 • 1 1 1 

•M" 


Q) 

> 

O 

O 

>« 

CL 

o 

c 

CO 

O 

■M 

C 

<0 

0 

1  

Cl) 

CL 

TJ 

C 

CO 

a> 

n 

E 

3 


-o 

c 

CO 

CO 


t-~- 

o 

CM 

id 

LU 


CD 

O 

CM 

i 

id 

LU 


in 

o 

CM 

■ 

id 

LU 


•M" 

O 

CM 

id 

LU 


m o ' 1 1— 

co 


■ i i ■ 


in  o 

-M- 


in  o 
m 


m o 
m 


■ i i i i 


■ ■•it 


■ ■■lit 


co 

o 

CM 

id 

LU 


in  o ' 1 1 1 1 1 1 

is- 


CM 

o 

CM 

£ 

LU 


o o 

CD 


O 

CM 

i 

LU 


in  o l— 
CD 


« 

w 

QJ 

O 

CD 

Cl 

(0 


a) 

n 

5 

o 

c 

CO 


Cfl 


-Q 

■Q 

CO 


c c 


CD 
.Q 
a> 

$ E ° 

- co  •— 


d a; 
n c 
a>  cc 
a)  tc 
co  i- 
w a 


<d  <d  a>  o 2 > <n  < 

d.  m c/>  = i_  c.  _ ; 

r — 1 /1\  OJ  - 


i/T  CL  O L-  3 CD 

<CDCd>ococQa 


in  m m 1 | — 

CM 


o o m m 

CD  i-  T_ 


m m o 1 t— 
Tj-  co 


in  in  o 
t-  co 


in  m in  1 1 

T — T — CO 


m m m 

M" 


m m m 1 H 
co 


in  o o 1 1— 

v-  CO 


in  m m 1 I— 

M" 


in  o m 


m 


o 

CM 


i/> 

CD 

(/> 

co 

co 


O 


co 

-Q 

o 

u_ 


o 

co 

® ai  O 


CO 

DO 


o 

cd 


willow  (Salix  spp.),  currant  (Ribes  spp.),  serviceberry  (Amelanchier  alnofolia).  big  sage  (Artemisia  tridentata), 
and  silver  sage  (A.  cana). 


18 


0 

O 

CO 


0 


c 

'to 

CO 

m 

£ 

o 

c 

c 

o 

O 


0 

E 

o 

< 


0 

0 

O 

0 

■C 

c 

o 

«/) 

T3 

C 

0 

to 

c 

0 

CL 

CO 

co 


CO 

o 

CL 

E 


(0 

0 

o 

0 

CL 

to 

£ 

o 

£ 

0 

T3 

c 

D 


0 

JQ 

TO 


C\J 

CO 

CM 

in 

•4 — 

CO 

CM 

£ 

in 

o 

CO 

CM 

X 

in 

CD 

CM 

CM 

* 

in 

l— 

oo 

0 

CM 

> 

CM 

o 

O 

i 

* 

in 

>s 

Q. 

O 

C 

CO 

O 

r-- 

CM 

CM 

c 

X 

0 

in 

p 

0 

a. 

CO 

•a 

CM 

c 

CM 

CO 

l_ 

0 

in 

.Q 

E 

3 

Z 

o 

CM 

■O 

CM 

| 

c 

* 

CO 

in 

(0 

CO 

T — 

CM 

* 

in 

00 

T — 

CM 

* 

in 

t'- 

T“ 

CM 

* 

in 

CO 

T — 

CM 

X 

in 

CO 

0 

o 

8. 

(0 

in  o 


■ i i i • ■ • 


n 


in 


m • ■ 1 H- 


■ i i i 


in  • ■ 1 1— 


• i i ■ 


in  o 1 1 1 1 1 1 1 

in 


o 

co 


o 

co 


in 


in 


in 


m o 


■ i i ■ i i i 


in  in  • 1 


o ■■■■■>  in 
tj- 


i i m • i m m 


o 

in 


in 

r- 


I—  h-  H h- 


in  o 
co 


_ o 

o co 


jc 

(O 

2 

-Q 

£ 

jQ 

TO 


£ 

r> 


■Sec  ^ 

5 0 0 0 0 
0 0.0)10  = 

C (0  I-  o 5 O 0 

w < o a:  > o c/) 


I s 


JC 

to 

I ^ 

C 0 

_Q  co 

0 TO 

CJ>  io 
TO  t- 
(O  0 

O)  ^ 

in  w 


in 


in 


in 

■m- 


o 

in 


in 

in 


m 

co 


in 

r- 


o 


o 

CO 


o 

CO 


o 

CO 


o 

CO 


in 


m m f- 


m in  |— 


in 


I-  o h- 


H o h- 


in 


H o (- 


in 


m 


in 


o 

uo 


<o 

0 

8 

TO 

o 


CO 

€ 

o 

LL 


O 

CO 

2 O 

CD  ^ o 

m j a: 


19 


CD 

O 

03 


CD 


C 

co 

03 

CD 

co 

■ 

o 

c 

c. 

o 

O 


<D 

E 

o 

< 


CD 

CD 

Q 

CD 

SZ 

c 

o 

C/3 

T3 

C 

03 

00 

C 

(D 

Q. 

c/o 

03 


c 
O 
L— > 

V) 

o 

Q. 

E 

o 

o 

C/3 

CD 

'o 

CD 

CL 

CO 

2r- 

o 

-1 — 4 

CO 

t_ 

CD 

■a 

c 

D 


o- 

_ao 

xo 

03 


CD 

> 

o 

o 

>4 

Q. 

o 

c 

03 

O 

c 

CD 

O 

!_ 

CD 

a. 

T3 

C 

03 

t_ 

(D 

jQ 

E 

3 


■a 

c 

TO 

CO 


CD 

co 

CM 

LU 


co 

CM 

LU 


oo 

ao 

o 

CD 

CL 

CO 


if)  o 

CD 


UO  o 

I"- 


if) 


in 


m 


in 


m 


in  1 (— 


jC 

cn 

3 

u_ 

DO 


10 

3 


CO 


-Q  t C CD 

X3  CD  X3  CO 

03  -Q  CD  03 

^ CD  O)  CO 

C C $^  0 03  1- 

CD  CD  CD  O 2 


CL  CD  </> 


cn  cd 


CD  — 


lO  >—  U > UJ  

<oq;5uwcqw 


CO 

CD 

co 

CO 

03 

5 


CO 

xo 


o 

CO 

£ a>  ^ 


03 

CD 


o 

o 

LT 


20 


Figure  2.  Unburned  aspen  stand  EK-214  in  the  Connors  Basin  Field,  Deeth 
Allotment.  Most  aspen  stand  in  this  pasture  regenerated  during  the  early  1980’s 
when  this  part  of  the  allotment  was  destocked  due  to  permittee  bankruptcy.  Note 
the  6 foot  red  and  white  survey  pole  for  scale  Print  from  color  slide  (Appendix  C 
- - No.  147)  by  Charles  E.  Kay;  August  29,  2002. 


21 


Figure  3.  Unburned  aspen  stand  EK-227  in  the  Connors  Basin  Field,  Deeth 
Allotment.  This  is  another  example  of  the  regeneration  event  that  occurred  in 
this  pasture  when  the  range  was  temporarily  destocked  during  the  1980’s  due  to 
permittee  bankruptcy.  The  large  trees  are  18-20  in.  DBH  and  110  years  old 
(Table  2).  Survey  pole  (6  ft.)  for  scale.  Print  from  color  slide  (Appendix  C - - No. 
279)  by  Charles  E.  Kay;  August  31 , 2002. 


22 


Figure  4.  Burned  aspen  stand  EK-232  in  the  Connors  Basin  Field,  Deeth 
Allotment.  Judging  by  the  size  of  the  dead  aspen  stems  in  the  photograph,  this 
aspen  stand  experienced  a major  regeneration  event  during  the  early  1980’s 
when  the  range  was  temporarily  destocked.  Then  in  2001 , the  stand  was  swept 
by  the  Stag  Mountain  wildfire  and  subsequently  resrouted  at  33,768  stems  per 
acre  (Table  1 ).  Survey  pole  (6  ft.)  for  scale.  Print  from  color  slide  (Appendix  C - - 
No.  324)  by  Charles  E.  Kay;  August  31, 2002. 


23 


Figure  5.  Aspen  stand  EK-217  in  the  Connors  Basin  Field,  Deeth  Allotment. 
After  this  stand  was  swept  by  wildfire  in  2001 , it  resprouted  at  59,161  stems  per 
acre,  the  highest  density  recorded  in  this  pasture  (Table  1).  Survey  pole  (6  ft.) 
for  scale.  Print  from  color  slide  (Appendix  C - - No.  170)  by  Charles  E.  Kay; 
August  29,  2002. 


24 


Figure  6.  Aspen  stand  EK-228  in  the  Connors  Basin  Field,  Deeth  Allotment. 

This  stand  also  burned  during  the  2001  fire  event,  but  it  resprouted  at  only 
10,251  stems  per  acre  (Table  1).  Also  note  the  extensive  bare  soil.  Survey  pole 
(6ft.)  for  scale.  Print  from  color  slide  (Appendix  C - - No.  286)  by  Charles  E.  Kay; 
August  31, 2002. 


25 


Deeth  Allotment  - Hanks  Creek  Basin  Field 

This  pasture  is  at  lower  elevation  than  Connors  Basin  Field  and  contains 
only  a handful  of  widely  scattered  aspen  stands,  three  of  which  are  protected  by 
exclosures.  The  East  and  West  Hanks  Creek  Exclosures  were  constructed  in 
1995,  while  the  Antelope  Basin  Exclosure  was  built  in  1997  (Appendix  A).  Plot 
EK-209  was  established  in  the  East  Hanks  Creek  Exclosure,  while  transect  EK- 
210  was  placed  inside  the  West  Hanks  Creek  Exclosure  - - there  are  no 
unprotected  aspen  at  either  of  these  locations.  Plot  EK-21 1 was  placed  inside 
the  Antelope  Basin  Exclosure,  while  transect  EK-21 2 was  placed  in  an  adjacent 
stand  grazed  by  cattle  (Appendix  A).  This  pasture  was  not  rested  in  2002,  as  it 
was  not  burned  by  the  Stag  Mountain  Fire. 

Aspen  inside  all  three  exclosures  successfully  regenerated  after  the  areas 
were  fenced  (Tables  5 to  7;  Figures  7 and  8).  At  the  time  they  were  sampled, 
however,  mule  deer  had  browsed  100%  of  the  aspen  suckers  inside  the  West 
and  East  Hanks  Creek  Exclosures  and  40%  of  the  suckers  inside  the  Antelope 
Basin  Exclosure  (Table  1;  Figure  9).  Aspen  sapling  density  inside  the  Antelope 
Basin  exclosure  was  six  times  that  on  the  unprotected  plot  (Table  1;  Figure  10). 
Grass  and  forb  canopy  cover  were  also  greater  inside  the  exclosure,  while  bare 
soil  was  more  common  on  the  unprotected  plot  (Table  7).  Unlike  aspen  in 
Connors  Basin  Field,  aspen  stands  in  the  Hanks  Creek  pasture  did  not 
experience  a regeneration  event  during  the  early  1980’s  (Tables  5 and  6). 


26 


0 

-g 

'«/> 

c 


CM  0 
^ 3 
UJ  j§ 

a)  o 

E x 

3 d) 

V) 

o .E 

(J  1/3 

X ™ 

(D  CD 

-X  CD 
CD  Q_ 

2 o 

O £ 
C/)  5 
-X  < 

m <D 

x£ 

S | 

LU  a 
—— 
CD  3 
JC  O 


CD 


CM 


2 CM 
£ * 


O) 

o 

CM 

I 

* 

LU 

T3 

0 

LL 


LU 

0 
w 
=3 

a 
o 
o 
X 
0 

c 

1/3 

_ CT3 

•55  OQ 
0 

CD  a. 

^ o 

0 0 

O < 

A 0 
-X  x: 
c *- 
ro  0 
x -g 

cfl 

0 __ 

E - 
o ™ 
=■  * 
< LU 

£ -g 
0 c 

CD  CO 

o 


0 


0 


=J 
5=  A 
C o 

° X 

0 

03  CD 

E 2 

CO  O 
TO  C/3 

32  co 

£ I 

TO  A 
C £ 
0 < 
CL 

A 0 

< 

4-1 

m 

0 

-Q 

CO 


0 

_Q 

E 

3 

Z 

■a 

c 

CO 

W 


CM 

T — 

CM 

* 

LU 


CM 

X. 

LU 


O 

CM 

i 

* 

LU 


O) 

o 

CM 

i 

:*: 

LU 


03 

Z 

UJ 

LU  Z 

o 

£ 

o 

o 

CM 

o 

03 

o o 

CM 

CM 

m 

M' 

m 

o o 

Is- 

z 

T— 

m m 

CO 

X 

CO  CO 

o 

co  h- 

co  m 

I**- 

O' 

03 

z 

LU 

UJ  z 

o 

<; 

o 

o 

CM 

O 

03 

o o 

CM 

CM 

m 

M1 

m 

o o 
m r-- 

CO  CO 

Is- 

co 

z 

O 

X 

o 

co  r- 
co  in 

r- 

03 

z 

LU 

UJ  z 

o 

LU 

O 

o 

T“ 

o 

03 

o o 

CM 

CO 

m 

M- 

m 

m o 
Is-  CM 
c-  co 

m 

co 

1 

o 

a 

o 

CO  h- 

o 

co  m 

M" 

o 

z 

UJ 

UJ  z 

o 

£ 

o 

o 

CM 

o 

03 

o o 

03 

CM 

in 

■M" 

m 

o m 
m co 
00  00 

•M- 

co 

z 

1 

o 

T— 

X 

o 

CO  C— 

co  in 

-M- 

•m- 

O 

O 


O 

O 


co  r-  o o 
r~~  co 

CM 


co 


o o 


o 

■M- 


O CO  O O -M- 

o co 

CO  CO  T- 

f'- 


o o o 


A 

0 


o tj-  m o o i"~ 

O O CO  CO 

t—  co  co 


o o o 


o 

o 


CM  'O'  O O 
r-  03 
■o  -O’ 

cm  m 


r~- 

co 


O O T- 


c 

o 

o 

x: 

in 

c 

$ 

0 

C3> 

c 

2 

•B 

co 

> 

T5 

0 

CL 

0 

o 

TO 

P 

<1) 

<n 

CO 

h- 

a 

=> 

LU 

< 

>p 

o' 

0 

CL 

O 

C0 


A 

T3 

>> 

0 

N 

A 

T3 

C 

TO 

4-4 

CO 


i£ 

2^ 
0 e 

Sz 

S*f 

a. 


■a 

0 

A 

£ 

o 

I— 

n 

2 

0 

-JC 

o 

3 

(0 


0 

L_ 

o 

CO 


A 

0 

'55 

c 

0 

T3 


X 

DO 

o 

« 

d 

CM 

V 

X 

CD 

a 

X 

CD 

Q 

X 

CD 

O 

</> 

Q. 

3 

2 

V 

d 

d 

d 

O)  03 

® $ 
CO 


* -r 

CO  CM 


CO 


CO 

A 


03  X=  0 
= TO  x: 

03  o co 

CL 


0 

0 

a 


L 

0 

TO 

£ 


27 


Table  6.  Age  and  diameter  of  aspen  on  the  Deeth  Allotment,  Hanks  Creek  Basin  Field.  R=stem  with  heart  rot 
that  could  not  be  aged. 


Stand  Number 

Stem  Diameter  (inches)/Age  (yrs) 

EK-209 

1*/7,  1*/7,  8/R,  9/72,  9/R 

EK-210 

20/122,  21/R,  21/125 

EK-21 1 

13/70,  18/R,  19/R 

EK-212 

13/75 

‘Stem  aged  at  ground  level. 


28 


CD 

O 

(0 


T3 

0) 

L_ 

c 

<75 

co 

CD 

CD 

2 

O 

CA 

C 

CO 

X 

*-T 

C 

<D 

E 

o 


<d 

CD 

Q 

<D 


C 

o 

(A 

■a 

c 

CO 

Ta 

c 

CD 

a. 

(A 

CO 

o 

c 

o 

'xt 

<A 

o 

CL 


o 

o 

(A 

CD 

O 

CD 

CL 

(A 

£ 

O 


CD 

T3 

C 

D 


h- 

jd 

JQ 

CO 


CD 

> 

o 

O 

>. 

CL 

O 

c 

CO 

O 

c 

CD 

s 

CD 

CL 

TD 

C 

CO 

<D 

X) 

E 

3 


■a 

c 

TO 

55 


CM 

* 

LU 


O 

CM 

i 

* 

LU 


O 

CM 

LU 


CD 

O 

CM 

i 

* 

LU 


« 

<A 

CD 


8. 

w 


io  m (—  in 

CM  t- 


o o 

CM  CM 


m 


m 


m m |— 


m o m (—  h-  t— 

CM  CM 


o m m i— 

CO  t- 


m 

CM 


in 

co 


o 

co 


m 


<A 

^ £ 


CD 

CD 


<D 
XI 
£ 

,g>  c 

CD  W 


2 


<A 

E 

XI 

.■t: 

X) 

XI 

CO 

c 

<z 

CD 

CD 


5 

E 

€ 

CD 

1 


CD 

X 
O 
CD 

o 

XI 


CA 

E 

X) 

CD 

O) 

CO 

” ? 
CD  O 
> = 


omoow 


CD 

CA 

O 

UL 


£ 

8 

8 

E 

CD 

(/) 


CA 

a> 

8 

CO 

l _ 

O 


CA 

■e 

o 


in  • 
co 


m o h- 


m m i— 


m m |— 


o 

CA 


e ® o 

CB  C O 

CD  Zi  CL 


* 


Bitterbrush  (Purshia  tridentata)  and  chokecherry  (Prunus  virginiana). 


29 


Figure  7.  Aspen  stand  EK-209  inside  the  East  Hanks  Creek  Exclosure,  Hanks 
Creek  Basin  Field,  Deeth  Allotment.  After  this  stand  was  fenced  to  exclude 
cattle,  it  successfully  produced  new  stems  greater  than  6 feet  tall.  Aspen  sapling 
density  on  this  plot  was  5,494  stems  per  acre  (Table  5).  Survey  pole  (6  ft.)  for 
scale.  Print  from  color  slide  (Appendix  C - - No.  51 ) by  Charles  E.  Kay;  August 
29,  2002. 


30 


Figure  8.  Aspen  stand  EK-21 1 inside  the  Antelope  Basin  Exclosure,  Hanks 
Creek  Basin  Field,  Deeth  Allotment.  After  this  stand  was  fenced  to  exclude 
cattle,  it  successfully  produced  new  stems  greater  than  6 feet  tall.  Sapling 
density,  however,  was  only  603  stems  per  acre  (Table  5).  Survey  pole  (6  ft.)  for 
scale  Print  from  color  slide  (Appendix  C - - No.  99)  by  Charles  E Kay;  August 
29,  2002. 


31 


Figure  9.  Aspen  sucker  inside  the  West  Hanks  Creek  Exclosure,  Hanks  Creek 
Basin  Field,  Deeth  Allotment.  All  aspen  suckers  inside  this  exclosure  had  been 
repeatedly  browsed  by  mule  deer,  which  limited  height  growth  and  sapling 
recruitment  (Kay  and  Bartos  2000).  Red  and  white  survey  pole  in  one  foot 
increments  for  scale.  Print  from  color  slide  (Appendix  C - - No.  83)  by  Charles  E. 
Kay;  August  29,  2002. 


32 


Figure  10.  Aspen  stand  EK-212  outside  the  Antelope  Basin  Exclosure,  Hanks 
Creek  Basin  Field,  Deeth  Allotment.  Unlike  its  fenced  counterpart  (Figure  8),  this 
unprotected  aspen  stand  has  not  been  able  to  successfully  produce  new  stems 
greater  than  6 feet  tall  except  where  individual  suckers  have  been  protected  from 
livestock  by  fallen  trees  or  thick  brush  (Vera  2000:132-162;  Kay  2001a,  2002; 
Ripple  and  Larsen  2001 ).  Print  from  color  slide  (Appendix  C - - No.  1 07)  by 
Charles  E.  Kay;  August  29,  2002. 


33 


Stag  Mountain  Allotment  - - McIntyre  Field 

McIntyre  pasture  in  the  Stag  Mountain  Allotment  is  located  to  the  west  of 
Connors  Basin  Field  on  the  Deeth  Allotment.  Thus,  Stag  Mountain  and  adjoining 
areas  have  essentially  been  divided  into  two  allotments  on  which  the  general 
climate,  soils,  and  such  are  similar,  but  with  different  grazing  histories.  While  the 
Deeth  Allotment  is  grazed  by  cattle,  McIntyre  Field  has  been  grazed  both  by 
cattle  and  domestic  sheep.  In  addition,  the  Stag  Mountain  Allotment  was  not 
destocked  during  the  early  1980’s,  as  was  Connors  Basin  Field.  This  difference 
in  grazing  history  is  reflected  in  the  condition  and  trend  of  aspen  on  these 
adjacent  pastures.  While  most  aspen  stands  on  the  east  side  of  Stag  Mountain 
experienced  a major  regeneration  event  during  the  early  1980’s  and  are 
generally  in  good  to  excellent  ecological  condition,  the  same  is  not  true  of  aspen 
immediately  to  the  west  on  the  adjoining  allotment. 

Instead,  aspen  in  the  McIntyre  Field  is  generally  in  very  poor  ecological 
condition  and  few  stands  have  successfully  produced  new  stems  greater  than  6 
feet  tall  except  at  the  uppermost  elevations  far  from  water  (Holecheck  1988,  Kay 
2001a,  2002;  see  Tables  8 to  10  and  Figures  1 1 to  16).  Many  aspen  stands  in 
this  pasture  have  been  reduced  to  only  a handful  of  live  stems,  while  other 
clones  have  been  completely  eliminated.  In  addition,  there  was  no  regeneration 
event  during  the  early  1980’s  west  of  the  divide  as  there  was  on  the  range 
immediately  to  the  east.  Moreover,  the  few  aspen  stands  in  McIntyre  Field  that 
have  regenerated  have  done  so  only  in  the  last  few  years  when  use  by  domestic 


34 


sheep  has  been  curtailed.  According  to  BLM,  a change  in  herders  occurred  on 
the  Stag  Mountain  allotment  a few  years  back  and  the  upper  portions  of  this  field 
have  not  been  grazed  by  sheep  since  that  time.  Cattle  use  on  McIntyre  Field, 
which  is  under  the  control  of  a different  permittee,  has  not  changed  at  least  not  to 
any  degree  that  has  allowed  aspen  to  recover. 


Table  8.  Aspen  stand  parameters  on  the  Stag  Mountain  Allotment,  McIntyre  Field. 


35 


CD 

.Q 

E 

3 

Z 

-a 

c 

TO 

w 


M- 

CM 

i 

id 

LU 


O 

-M- 

CM 

* 

LU 


CT) 

CO 

CM 

i 

id 

LU 


oo 

CO 

CM 

id 

UJ 


CO  Z 

LU 

LU 

Z 

o 

oo 

o 

o 

CD 

m 

o 

o 

o 

00 

CD 

T — 

CT) 

CO 

OO 

CD 

m 

in 


02  LU 
CM  OO 
ID 


o z LU 

CM  t-  OO 

cd  "M-  m 


o Z LU 

CO  -r-  00 
in 


UJ 

o 

o 


o 

o 


c 

o 

t3 

CD 

CO 


V)  (D 


cm  in 

ct>  e- 

CM  OO 

cd  in 


UJ  Z 

O O 

o o 

CT>  CT) 

oo 

CM  OO 

co  in 


Ul  Z 
o o 
o o 

1-  CO 
oo  m 
cm  oo 
co  in 

■M- 


O 

co 

CT) 

CO 


O 

O 

CO 

Is- 


O 

O 

CM 

Is- 


UJ 


O 

CM 


m 


UJ 


o 

CO 

I 

m 


o 

o 

co 

X 

o 

in 


o 

o 

co 

X 

o 

CO 


o 

CO 

s 

o 

oo 


o 

o 

X 

o 

Is- 


< 

z 


co  in 

M- 


T — 

O)  Z 

Ul 

Ul 

z 

o 

CNJ 

o 

oo 

o 

o 

CM 

CM 

■M- 

m 

o 

o 

CO 

v 

CM 

CO 

h- 

LU 

o 

CO 

CM 

oo 

CO 

m 

C 0 


o 

o 

3 

o 

co 


< 

Z 


o> 

c 

ro 

Cd 


t— 

D 


c 

o 

CO 

> 

a> 

UJ 


CD 

Q. 

</> 

< 


CD 

CL 

_o 

CO 


</) 

T3 

>* 

CD 

N 

"c/> 

■a 

c 

CO 

(0 


|£ 

CD  C 
C — 
<D  -C 
CJ)  O) 
CD  XZ 

Od 


CO 


O 

O 


O 

O 


■a 

CD 

</) 

$ 

2 

jQ 

£ 

CD 

O 

3 

CO 


CD  r-  CD  N OO 
■<t  N CO  CO  CD 

in  oo  "M"  cm 

CM 


O O O h- 
00  CO 

00 

CM 


o o o o o 


o o o 


0)0  0 


M-  O O 


o o o o 

in 

CO 

CO 


Is- 

CD 


T-  O O 


in 

CD 

>- 


cn 

CD 

>- 


</) 

(D 

>- 


e'- 

o  z 

LU 

UJ  Z 

o 

LU 

o 

o 

o 

o 

o 

en 

CO 

oo 

O O 

o 

z 

-M" 

in 

Is- 

-M- 

in 

CM 

■ 

id 

■M- 

m 

in  in 

CO  t- 

co  m 

■M- 

e- 

S 

o 

co 

co 

LU 

CM  oo 
co  m 

CO 

•M- 

m 

r-  z 

Ul 

LU  z 

o 

Ul 

O 

o 

< 

O 

e'- 

co 

CM  P- 

00 

o o 

oo 

</d 

t — 

o 

z 

O 

er) 

CM 

■ij- 

m 

o o 

Is- 

CO 

T — 

T — 

id 

O T~ 
CM  Is- 

co 

X 

o 

CO 

CM 

LU 

co  oo 

o 

co  in 

-M- 

CO 

oo  z 

LU 

UJ  z 

o 

LU 

in 

o 

< 

O 

CM 

CO 

CM 

co 

O O 

o 

oo 

z 

O 

CM 

CM 

•s? 

in 

o in 

CT) 

X 

t — 

t— 

1 

id 

CT)  CM 

T-  co 

CO 

o 

■M- 

LU 

CO  oo 
co  in 

Tf 

m 

m-  z 

LU 

Ul  Z 

O 

CO 

m 

o 

o 

m 

o 

CM 

o 

oo 

O O 

O 

T— 

in 

in 

■M- 

■M- 

CM 

■M" 

m 

m in 

CT) 

T — 

co 

id 

Ul 

1-  CO 
O CM 
CO  oo 

e^ 

X 

o 

o 

T — 

co  m 

T — 

M- 

M- 

^ Z 

UJ 

Ul  Z 

o 

LU 

o 

o 

o 

o 

CT) 

CM 

o 

oo 

O O 

CM 

C/D 

CM 

m 

o 

CM 

O 

CM 

id 

Ul 

•M- 

in 

o o 

00  -M- 
O)  CM 
CM  OO 

Is- 

Is- 

2 

o 

o 

m 

00 

co  in 

T~ 

■M- 

CO 

M-  Z 

LU 

LU  z 

o 

UJ 

O 

o 

< 

O 

CM 

CM 

O 

oo 

O O 

■M- 

C/D 

CM 

o 

z 

O 

T— 

CM 

i 

id 

Ul 

"M" 

in 

m o 

o CM 
CO  00 

co  m 

-M- 

Is- 

y 

o 

oo 

■M- 

CM 

CM 

O)  Z 

LU 

UJ  z 

O 

O 

o 

< 

< 

O 

CM 

o 

00 

O O 

CM 

c/d 

CM 

o 

z 

z 

CM 

i 

id 

Ul 

•O' 

m 

o in 
cm  e- 
o o 
co  oo 

CM 

Is- 

1 

m 

CO 

X 

o 

o 

CO 

■M" 


M- 

CO 


■M- 

CO 


o o 


o o o o 


00  o o 


in 

CD 

> 


o o o o 


Is-  O O 


CO 


CO 


■M- 

CO 


-M- 

CO 


CM  O O 


o 

Z 


o o 


o 

CM 


O O O Is- 

co 


o o o o o 


o o 


r-  o o 


0)0  0 


o o o o o 


O O 


in 

CD 

> 


m 

CD 

>- 


CD 

l— 

o 

CO 
' — * 

CO 

CD 


c n 
c 
CD 

■a 


X 

00 

O 


X X 
OO  CQ 
Q Q 


E ^ 
a3  co 
v 

(/) 


CM 

V 

V 

C M-  oo 

i i 

CO  CM  Tt 


X 

CO 

o 


.E  d 


oo 

A 


« 

in 

Cl 

3 

O 

O)  OJ  CL 
■ . — 0) 

(D  t;  CD  CD 
= ra  £ CD 

CD  o W Q 
CL 


i. 

CD 

ts 

£ 


Pellet  groups  per  2x30  m (6.6  x 98  ft.)  belt  transect.  **Water  in  or  near  stand.  NA=Not  applicable. 


Table  8.  Aspen  stand  parameters  on  the  Stag  Mountain  Allotment,  McIntyre  Field. 


36 


3 

E 

zj 

z 

T3 

C 

OB 

V) 


cm 

m 

CM 

I 

LU 


in 

CM 

i 

* 

LU 


O 

in 

CM 

i 

* 

LU 


CT> 

M- 

CM 

id 

LU 


00 

CM 

i 

* 

LU 


r-- 

■m- 

CM 

I 

id 

UJ 


CD 

ifr 

CM 

i 

* 

UJ 


m 

■m- 

CM 

I 

id 

UJ 


M- 

-M- 

CM 

i 

id 

UJ 


CO 

■M- 

CM 

i 

* 

LU 


CM 

•M- 

CM 

i 

id 

LU 


05  z LU 

LU  Z 

O 

UJ 

o 

o 

o 

o 

co  05  o o m 

CM  O O 

CM  ^ oo 

O O 

CM 

z 

CM 

o 

o 

o 

OO  O CO 

M-  m 

o o 

O CM 

CO 

1 

o 

T— 

3 

r*» 

CM  oo  CO 

CO  1— 

CM  Z LU 
T-  CO 
o-  m 


m 


Z UJ 

O CD 
Tt  m 


cm  z LU 

CD  T-  00 

•M-  m 


co 


co 


co 


Z UJ 
T-  oo 
■O-  m 


Z UJ 
t-  oo 
rt  m 


Z UJ 
T-  oo 
M-  m 


c x: 

O <A  05 

■c  i 

<u  o 
CO  L— 


cn 

c 

co 

0^ 


o in 
co  oo 
co  m 


UJ 

o _ 
m in 


r-'- 

05 


co 


CM  OO 

co  m 


UJ  Z 
o o 
o o 

O)  CO 
oo  CM 
CM  OO 

co  m 

■M- 


UJ 

o 

o 


o 

m 


CM  CO 
05  CO 
CM  00 

co  m 


LU 

o 

o 


o 

in 


in  co 
oo  CO 
CM  OO 

co  m 


UJ 

o 

o 


Z 

o 

o 


00  05 
OO  CO 
CM  OO 

co  in 


LU  Z 
o o 
o o 

OO  CM 
OO  M- 
CM  00 

co  m 

•M- 


o 

oo 

CO 

r- 


o 

■M" 

co 

I"- 


o 

■M" 

■M" 

r-'- 


o 

co 


o 

oo 

CM 

h- 


o 

CM 

m 


UJ 


m 


£ 

Z 


UJ 

w 


LU 


o 

CO 

I 

m 


o 

CM 

in 


o 

CM 

I 

m 


m 


o 

co 


o 

CM 


o 

co 

T— 

X 

o 

00 


o 

m 

T — 

X 

o 

05 


o 

co 

X 

o 

CM 


o 

o 

s 

o 

o 

CM 


O 

in 

X 

o 

co 


o 

t'- 

X 

o 

CM 


o 

o 


o 

o 


o 

o 


o 

o 


o 

o 


o o o 


I"- 

oo 


O CM  oo 
1-  O CO 
O g CM 
CM 


r- 

co 


r"-  o o 


O M- 

co 


CO  o o 


05 

CO 

■sf 


o o o 


r-- 

CD 


m o o 


co  o o o r — 
Is-  co 

CM 


o o o o o 


oo  o o 


o o 


< 

z 


05 

Z 

UJ 

UJ  z 

o 

UJ 

o 

o 

CM 

oo 

o o 

o 

CM 

o 

in 

o o 

CM  O 

CO 

h- 

§ 

O CO 

o 

o 

o 


o 

o 


CM  O 
o 

M- 


o o 


r- 

CO 


o o 


m o o o co 
h-  o 

CO  CO 


CM  O O 


CO  oo 
co  m 


r,  z 

UJ 

UJ  z 

o 

LU 

o 

o 

< 

o 

f— 

o 

o 

O M- 

CM  T- 

oo 

o o 

oo 

z 

T— 

1^ 

z 

o 

T — 

CO 

Tt 

m 

o in 

05 

T — 

T — 

CM 

’I 

CO  05 

CO 

X 

CM 

co 

o 

co  oo 

o> 

co  in 

it 

CO  Z 

UJ 

UJ  Z 

o 

z 

o 

o 

< 

< 

o 

o 

o 

o o 

r*  ^ 

00 

O O 

o 

o 

z 

z 

m 

o o 

CO 

CO 

m 

2 

O oo 

o 

CO  00 

oo 

co  m 

M- 

M;  z 

UJ 

UJ  Z 

o 

UJ 

o 

o 

o 

o 

y- 

05 

oo 

O Tt 

CM  00 

co 

o o 

CM 

z 

CM 

in 

■M- 

r— 

CO 

CO 

co 

CM 

in 

o o 

05 

1 

Q 

T— 

CM 

"M" 

CM 

T — 

1-  CO 

o o 

CO 

X 

o 

CM 

05  (O 

CO 

moo 


o o o 


o o o 


in  tj- 


05 


2 

P 

D 


c 

o 

00 

> 

05 

LU 


ts 

I 

in 

< 


05 

CL 

O 

(/) 


in 

05 

^>; 

05 

N 

(/) 

TO 

CZ 

CO 

1 

W 


CO 

I 

Cl) 

c 

O)  O) 

5 2 


e 

O 

X 

■O 

CO 

GQ 

05 

in 

Q 

o^ 

TD 

<15 

t — 

O 

s 

JO 

12 

05 

v- 

05 

E 

m 

c 

05 

c X 
"8 

X 

00 

Q 

X 

00 

Q 

* 

m 

CL 

zb 

o 

!E 

"O  . 
c « 

v .E 

d 

d 

05  gj 

o 

c/> 


05  <D 
-S  V 
(J ) 


4=  O’ 
CO  CM 


0O 


OO 

A 


CL 

05  <- 
05  05 
£ co  r 05 
a>  O C/5  O 
Ol 


o 

Z 


in 

05 

>- 


in 

05 


m 

05 

>- 


m 

05 

>- 


in 

05 

>- 


o 

Z 


in 

05 

>- 


in 

05 


05 

CO 

5 


Pellet  groups  per  2x30  m (6.6  x 98  ft.)  belt  transect.  **Water  in  or  near  stand.  NA=Not  applicable. 


37 


Table  9.  Age  and  diameter  of  aspen  on  the  Stag  Mountain  Allotment,  McIntyre  Field.  R=stem  with  heart  rot 
that  could  not  be  aged.  Burned=recently  burned  stand  in  which  all  the  overstory  trees  were  killed 
and  thus  no  age  data  collected. 


Stand  Number 

Stem  Diameter  (inches)/Age  (yrs) 

EK-221 

EK-222 

EK-223 

EK-224 

EK-225 

EK-233 

EK-235 

EK-237 

EK-238 

EK-239 

EK-240 

EK-241 

EK-242 

EK-243 

EK-244 

EK-245 

EK-246 

EK-247 

EK-248 

EK-249 

EK-250 

EK-251 

EK-252 

No  live  stems  in  stand 

No  live  stems  in  stand 

10/95,  11/R,  11/97,  12/100 

1*/6,  1*/6,  1*/6,  2*/6,  2*/7,  11/R,  11/98,  12/R,  14/R 

279,  279,  279,  279,  2710,  3*/11,  13/95,  14/98,  15/100.  16/R 

Burned 

Burned 

1*/6,  1*/6,  1*/9,  2*/10,  2*/1 1 , 3/15,  3/15,  13/85,  13/87 
19/75,  20/R 
10/R,  11/R 
15/R,  16/R,  17/R 

1*/8,  1*/8,  3/17,  3/18,  4/23,  5/22,  6/26,  13/65,  21/88,  24/R,  26/R,  27/R 

No  live  stems  in  stand 

No  live  stems  in  stand 

17/90,  10/92,  24/R 

9/80,  10/80 

No  data  collected  - - see  original  data  sheet 
No  live  stems  in  stand 
16/87,  17/R 

No  data  collected  - - see  original  data  sheet 

176,  276,  276,  4/14,  5/14,  5/12,  14/R,  18/65,  19/77 
No  data  collected  - - see  original  data  sheet 

177,  179,  1710,  1710,  177,  1711, 2711,  9/76,  10/80,  11/80,  12/81,  18/102 

•Stem  aged  at  ground  level. 


38 


CD 

O 

CD 


T3 

CD 

U_ 

TO 

>» 

E 

o 


c 

TO 

E 

_o 

< 

c 

CD 

3 

3 

O 

O) 

TO 

GO 

CD 


c 

o 

CO 

T5 

3 

TO 

to 

3 

CD 

CL 

c/> 

CD 


3 

o 

L-* 

‘c/> 

O 

CL 

E 

o 

o 

c/> 

TO 

O 

TO 

CL 

CO 

£ 

O 


TO 

"O 

3 

D 


TO 

JD 

TO 

h- 


TO 

> 

O 

O 

>s 

CL 

O 

3 

TO 

O 
-•— * 
3 
TO 
O 

s 

TO 

CL 

■o 

3 

TO 

i— 

TO 

.Q 

E 

3 


~a 

3 

TO 

CO 


o 

M- 

CM 

i 

* 

ID 


o> 

CO 

CM 

t 

5^ 

LU 


CO 

CO 

CM 

i 

* 

LU 


I-'- 

co 

CM 

i 

LU 


m 

CO 

CM 

I 

LU 


CO 

CO 

CM 

I 

* 

LU 


in 

CM 

CM 

I 

Q 

LU 


O’ 

CM 

CM 

LU 


CO 

CM 

CM 

i 

* 

LU 


CM 

CM 

CM 

* 

LU 


CM 

CM 

i 

* 

LU 


« 

to 

TO 


& 

CO 


in  o 

CM 


m o 
in 


o 

CM 


in 


in  m 


1-  m 


m 


o 

M- 


O 

■O’ 


m 


o | — m 
m 


o 

CM 


m m (— 


m 


in  o 
co 


m 

co 


m 


m o 

CM 


o m 

CM  t- 


o o 

T-  -M- 


m 


o 

co 


o 

co 


o 

CM 


m 


m 


m 


o 

co 


m o (— 


m o i— 


m 


m m h h 

CM 


in  m I— 


m 

co 


o 

CM 


m 


in  m 

CM 


o o t— 

CM  T- 


o 

CM 


I-  h- 


to 

E 

_Q 

TO 

cn 

CD 

to 


x: 

to 

E 

n 

n 
n 

TO 
u 

3 3 


co 

E 

n 

25 

m JZ 

to  w 

I E 

s -e 


TO 


E TO  TO  -Q 

U _ C_  m Ql  -LJ  _ \i> 

3 .5*  3 <-  to  3 £ •>  O 

cocooo<oc:oo>a: 


to 

CD 

CO 

CO 

TO 

O 


to 

■e 

o 


8 

£ * o 

TO  O 

CO  J CL 


Rubber  rabbitbmsh  (Chrysothamnus  nauseosus). 


39 


<D 

O 

ro 


ii 

I- 

33 

a> 

u_ 

CD 

' 

>- 

c 

o 


c 

CD 

E 

o 

< 

c 

to 

c 

to 

o 

0) 

to 

CO 

CD 


C 

o 
co 
"O 
c 
ro 
-*— < 
CO 

c 

CD 

CL 

CO 

ro 


co 

o 

Q. 

E 

o 

o 

co 

CD 

o 

CD 

Q. 

CO 

£ 

0 

to 

1  

0) 

T3 

C 

3 


0 

ra 

01 

H- 


CD 

> 

O 

O 

>. 

a. 

o 

c 

to 

O 


CD 

0 

1  

CD 

Q_ 

•a 

c 

03 

i 

CD 

XI 

E 

rj 

Z 

T3 

C 

CD 

CO 


CM 

io 

CM 

I 

UJ 


LO 

CM 

I 

UJ 


o 

LO 

CM 

X. 

LLi 


03 

M" 

CM 

I 

UJ 


oo 

M- 

CM 

I 

UJ 


h- 

M- 

CM 

I 

UJ 


CO 

M- 

CM 

* 

UJ 


LO 

M" 

CM 

i 

* 

UJ 


M" 

CM 

I 

* 

UJ 


00 

M- 

CM 

I 

UJ 


CM 

M- 

CM 

I 

* 

UJ 


M- 

CM 

I 

* 

UJ 


co 

QJ 

O 

CD 

a. 

CO 


LO 


O LO 

T-  co 


o o 
t—  co 


LO  o 

LO 


LO  LO  1 

co 


LO  LO 

T—  ^ 


o o 

T-  O' 


LO  O 1 


I-  CO 


o o 

T-  CO 


O LO 
T-  CM 


LO 


LO 


-C 

co 

ro 

^xj 

CD 


CD  -S 
co  5 
,S>  i 


CO 

ro 


XJ 

n 

ro 


co 


LO 


1 LO  (— 


h-  t— 


CO 

ro 


XJ 

m SZ 

03  CO 

^ ro 


C C 53  ^ 

CD  Q3  -9  m LJ 

CD  CL  -9  -2  = 

10  2 .t;  ^ 


$ 

o 


o 


O 

co 


LO 

CM 


LO 

CM 


O 

CO 


O 

CM 


LO 


LO 


LO 


LO  LO  | — 
CM  CM 


O LO  (— 


LO 


LO  LO  LO 


LO 


O LO  I— 


O LO  I— 


LO 


O LO  h- 


o 

CO 


o 

LO 


o 


o 


LO 

LO 


o 

CM 


LO 


LO  O K 


LO  LO  (— 
CM  t- 


LO  O | — 


I—  o | — 


CD  I- 


LO 


1-  l-  co  j .■e  ^ l-> 

wmocxcDD^a: 


CO 

CD 

co 

CO 

03 

0 


CO 
X3 
1 — 

O 

LL 


O 

CO 

£ © o 


TO 

00 


o 

o: : 


40 


Figure  11.  Aspen  Stand  EK-240,  McIntyre  Field,  Stag  Mountain  Allotment. 
Unlike  aspen  stands  on  the  east  side  of  Stag  Mountain,  which  are  generally  in 
good  to  excellent  ecological  condition  (Figures  2 and  3),  aspen  on  this  adjoining 
allotment  is  in  very  poor  condition.  Note  the  vehicle  for  scale.  Print  from  color 
slide  (Appendix  C - - No.  447)  by  Charles  E.  Kay;  September  1,  2002. 


41 


Figure  12.  Aspen  stand  EK-247,  McIntyre  Field,  Stag  Mountain  Allotment.  No 
live  stems  were  found  and  this  aspen  clone  is  now  dead.  Print  from  color  slide 
(Appendix  C - - No.  525)  by  Charles  E.  Kay;  September  2,  2002. 


42 


Figure  13.  Aspen  stand  EK-249,  McIntyre  Field,  Stag  Mountain  Allotment.  Only 
the  one  aspen  tree  seen  in  the  distance,  and  a few,  repeatedly  browsed  aspen 
suckers,  remain  alive  in  this  clone.  Print  from  color  slide  (Appendix  C - - No. 
542)  by  Charles  E.  Kay;  September  2,  2002. 


43 


Figure  14.  Aspen  stand  EK-251,  McIntyre  Field,  Stag  Mountain  Allotment. 
Judging  by  downed  trees,  this  aspen  clone  once  covered  nearly  an  acre  but 
repeated  livestock  use  has  prevented  recruitment,  and  the  stand  is  now  in 
danger  of  being  lost.  Note  the  vehicle  for  scale.  Print  from  color  slide  (Appendix 
C - - No.  568)  by  Charles  E.  Kay;  September  2,  2002. 


44 


Figure  15.  Aspen  stand  EK-239  viewed  northwest,  McIntyre  Field,  Stag 
Mountain  Allotment.  Most  of  the  area  between  the  camera  and  the  distant  trees 
was  once  a fully  stocked  aspen  stand,  but  repeated  livestock  use  has  killed-out 
most  of  the  clone.  Note  the  vehicle  for  scale.  Print  from  color  slide  (Appendix  C 
- - No.  41 8)  by  Charles  E.  Kay;  September  1 , 2002. 


45 


Figure  16.  Aspen  stand  EK-239  viewed  northeast,  McIntyre  Field,  Stag  Mountain 
Allotment.  While  large  areas  of  this  aspen  stand  now  lack  live  stems  (Figure  15), 
aspen  on  the  steeper,  more  distant  slopes  has  regenerated  in  recent  years,  as 
domestic  sheep  use  has  declined  on  this  joint-use  allotment.  Print  from  color 
slide  (Appendix  C - - No.  41 1 ) by  Charles  E.  Kay;  September  1 , 2002. 


46 


Cheveller  Exclosure  - McIntyre  Field,  Stag  Mountain  Allotment 

The  Cheveller  Exclosure  was  closed  to  livestock  in  1 991 . Prior  to  that 
date,  it  was  a fenced  private  pasture,  but  with  completion  of  the  Marys  River  land 
exchange  on  May  29,  1991,  it  became  public  (BLM).  The  Cheveller  Exclosure 
(EK-241, 242,  and  243)  is  built  along  an  unnamed  tributary  to  Stag  Creek 
(Appendix  A).  This  is  an  intermittent  stream  and  where  there  is  little  or  no  water, 
aspen  has  successfully  regenerated  (Tables  8 to  10;  Figures  17  and  18).  Mule 
deer,  however,  have  grazed  many  of  the  aspen  suckers  inside  the  exclosure 
(Figure  19)  and  likely  reduced  sapling  recruitment  (Kay  and  Bartos  2000).  In 
addition,  beaver  (Castor  canadensis)  have  damned  several  sections  of  the  creek 
and  cut  the  adjoining  aspen  (Figure  20).  Where  this  occurred  prior  to  the 
removal  of  livestock,  however,  long  sections  of  streamside  aspen  were 
eliminated  (Figures  21  and  22).  Aspen,  no  doubt,  regenerated  after  the  mature 
trees  were  felled  by  beaver,  but  all  the  new  suckers  were  repeatedly  browsed  by 
cattle  until  entire  clones  became  extinct  (Kay  2001a).  Again  this  occurred  only 
where  there  was  sufficient  water  in  the  stream  to  support  beaver.  Where  there 
was  little  or  no  water  in  the  stream,  beaver  could  not  colonize  those  areas,  and 
there,  aspen  survived  and  regenerated  after  livestock  use  was  eliminated. 


47 


Figure  17.  Fenceline  contrast,  Cheveller  Exclosure,  McIntyre  Field,  Stag 
Mountain  Allotment.  Cattle  have  been  excluded  from  the  area  to  the  left  of  the 
fence  since  1991 . Viewed  east  along  the  south  boundary.  Print  from  color  slide 
(Appendix  C - - No.  491)  by  Charles  E.  Kay;  September  1,  2002. 


48 


Figure  18.  Aspen  stand  EK-241  inside  the  Cheveller  Exclosure,  McIntyre  Field, 
Stag  Mountain  Allotment.  Where  the  intermittent  stream  is  dry,  the  mature  aspen 
trees  have  not  been  cut  by  beaver  and  aspen  has  successfully  produced  new 
stems  greater  than  6 feet  tall  since  livestock  were  excluded  in  1991 . Note  survey 
pole  (6  ft.)  for  scale.  Print  from  color  slide  (Appendix  C - - No.  455)  by  Charles  E. 
Kay;  September  1 , 2002. 


49 


Figure  19.  Browsed  aspen  sucker  inside  the  Cheveller  Exclosure.  Many  aspen 
suckers  inside  the  exclosure  have  been  repeatedly  browsed  by  mule  deer.  This 
likely  has  limited  sapling  recruitment  (Kay  and  Bartos  2000).  Red  and  white 
survey  pole  in  one  foot  increments  for  scale.  Print  from  color  slide  (Appendix  C - 
- No.  457)  by  Charles  E.  Kay;  September  1, 2002. 


50 


Figure  20.  A recent  beaver  dam  inside  the  Cheveller  Exclosure.  Where 
permanent  water  is  available,  beaver  have  cut  stream-side  aspen  inside  the 
Cheveller  Exclosure.  Aspen  has  resprouted,  but  many  of  those  suckers  have 
been  browsed  by  mule  deer,  threatening  stand  recruitment  (Kay  and  Bartos 
2000).  Print  from  color  slide  (Appendix  C - - No.  459)  by  Charles  E.  Kay; 
September  1 , 2002. 


51 


Figure  21.  Aspen  stand  EK-242  inside  the  Cheveller  Exclosure.  All  the  area 
along  the  stream  from  the  lower  right  of  this  photo  up  to  the  remaining  trees  was 
once  a fully-stocked  aspen  stand.  Beaver  then  colonized  the  area  and  cut  the 
mature  aspen  for  food  and  dam  building  materials.  Aspen  resprouted  but 
livestock  repeatedly  browsed  all  the  new  suckers  until  aspen  was  eliminated  (Kay 
2001  a).  This  occurred  prior  to  1 991 , when  livestock  were  excluded  from  this 
fenced  area  (see  text).  Where  this  intermittent  stream  is  dry,  beaver  did  not  cut 
the  mature  trees  and  aspen  survives  - - photo  upper  left.  Print  from  color  slide 
(Appendix  C - - No.  475)  by  Charles  E.  Kay;  September  1,  2002. 


52 


Figure  22.  Aspen  stand  EK-243  inside  the  Cheveller  Exclosure.  The  entire  area 
along  the  stream  in  this  photograph  was  once  a fully-stocked  aspen  stand. 

Beaver  then  colonized  the  area  and  cut  all  the  mature  trees.  Aspen  regenerated, 
but  livestock  repeatedly  browsed  all  the  new  suckers  until  aspen  was  eliminated 
(Kay  2001a).  This  occurred  prior  to  1991  when  livestock  were  excluded  from  this 
fenced  area  (see  text).  Most  deforested  areas  along  the  stream  in  the  Cheveller 
Exclosure  were  once  fully-stocked  aspen  stands.  Print  from  color  slide 
(Appendix  C - - No.  485)  by  Charles  E Kay;  September  1, 2002. 


53 


Beaver 

Similar  to  what  was  documented  in  the  Cheveller  Exclosure,  beaver 
activity  30  to  40  years  ago,  or  longer,  appears  to  have  contributed  to  the  decline 
of  several  aspen  stands  on  both  the  Deeth  and  Stag  Mountain  Allotments 
(Figures  23  to  26).  Beaver  often  improve  riparian  conditions  (Kay  1 994),  but  as 
the  aspen  trees  were  felled,  livestock  repeatedly  browsed  all  the  new  suckers 
until  entire  clones,  and  the  beaver  themselves  were  eliminated  (Kay  2001a). 


54 


Figure  23.  Recent  beaver  activity  on  an  unnamed  tributary  to  the  South  Fork  of 
Flanks  Creek,  Connors  Basin  Field,  Deeth  Allotment.  Beaver  colonized  this  area 
during  the  early  1990’s  and  cut  most  of  the  aspen  trees.  The  area  was  burned 
by  the  Stag  Mountain  fire  in  2001  and  then  the  dam  failed.  Shown  is  the  old 
beaver  dam,  lodge,  and  food  cache.  Note  the  vehicle  in  the  distance  for  scale 
(photo  right).  Print  from  color  slide  (Appendix  C - - No.  128)  by  Charles  E Kay- 
August  29,  2002. 


55 


Figure  24.  Old  beaver  activity  on  an  unnamed  tributary  to  the  South  Fork  of 
Hanks  Creek,  Connors  Basin  Field,  Deeth  Allotment.  At  some  point  in  the  past, 
beaver  colonized  this  area  and  cut  the  aspen  in  the  lower  portion  of  this 
photograph.  Livestock  then  repeatedly  browsed  all  the  new  aspen  suckers  until 
the  clone  was  eliminated.  This  did  not  happen  to  aspen  on  the  more  distant 
hillsides,  where  clones  experienced  a major  regeneration  event  during  the  early 
1980’s  when  this  pasture  was  temporarily  destocked  due  to  permittee 
bankruptcy.  Shown  in  aspen  stand  EK-220.  Print  from  color  slide  (Appendix  C - 
- No.  191)  by  Charles  E.  Kay;  August  30,  2002. 


56 


Figure  25.  Old  beaver  activity  on  Connors  Creek,  Connors  Basin  Field,  Deeth 
Allotment.  At  some  point  in  the  past,  beaver  colonized  this  area  and  cut  the 
aspen  along  this  portion  of  Connors  Creek.  Livestock  then  repeatedly  browsed 
all  the  new  aspen  suckers  until  large  areas  of  aspen  were  eliminated.  This  did 
not  happen  to  the  aspen  on  the  more  distant  hillsides,  where  those  clones 
experienced  a major  regeneration  event  during  the  early  1980’s  when  this 
pasture  was  temporarily  destocked  due  to  permittee  bankruptcy.  The  area  was 
subsequently  burned  by  the  Stag  Mountain  fire  in  2001 . Note  the  old  beaver 
dam  - - photo  lower  left  - - and  the  vehicle  for  scale  (photo  right  edge).  The 
entire  area  between  the  vehicle  and  the  old  beaver  dam  was  once  a fully  stocked 
aspen  stand.  Shown  is  aspen  stand  EK-231 . Print  from  color  slide  (Appendix  C 
- - No.  31 3)  by  Charles  E.  Kay;  August  31 , 2002. 


57 


Figure  26.  Old  beaver  activity  on  upper  Cottonwood  Creek,  McIntyre  Field,  Stag 
Mountain  Allotment.  Most  of  the  area  in  this  photograph  was  once  a fully  stocked 
aspen  stand  until  the  site  was  colonized  by  beaver  at  some  point  in  the  past. 

After  beaver  felled  the  mature  trees,  livestock  repeatedly  browsed  all  the  new 
aspen  suckers  until  the  entire  clone  was  eliminated.  The  beaver  dam  was  at  the 
far  end  of  what  is  now  a meadow.  Shown  is  aspen  stand  EK-222.  Print  from 
color  slide  (Appendix  C - - No.  234)  by  Charles  E.  Kay;  August  30,  2002. 


58 


Allotment  Comparison 

To  reiterate,  aspen  in  Connors  Basin  Field  of  the  Deeth  Allotment 
regenerated  during  the  early  1980’s  when  that  pasture  was  temporarily 
destocked  due  to  permittee  bankruptcy,  while  the  range  immediately  to  the  west, 
McIntyre  Field  on  the  Stag  Mountain  Allotment,  was  never  destocked,  and  those 
aspen  have  generally  not  regenerated  and  are  in  poor  ecological  condition  - - 
Connors  Basin  Field  is  grazed  only  by  cattle,  while  Stag  Mountain  Allotment  is 
grazed  by  both  cattle  and  domestic  sheep.  These  differences  can  be  seen  at 
the  allotment  boundary  (Figures  27  to  30).  Aspen  stand  EK-234  is  south  of  the 
allotment  fence  in  Connors  Basin  Field,  while  EK-233  is  north  of  the  allotment 
fence  in  McIntyre  Field.  EK-234  experienced  a major  regeneration  event  during 
the  1980’s,  while  EK-233  did  not.  Both  stands  were  burned  in  2001  by  the  Stag 
Mountain  fire.  Connors  Basin  Field  was  rested  in  2002  but  not  the  adjacent 
pasture;  i.e. , stand  EK-234  was  not  legally  grazed  by  livestock  in  2002,  while  EK- 
233  was  grazed  by  cattle.  Stand  EK-233  had  a sucker  density  of  1 1 ,122  stems 
per  acre,  while  across  the  fence,  EK-234  produced  49,900  suckers  per  acre 
(Figures  29  and  30).  Where  grazed  (EK-233),  the  mean  aspen  sucker  height 
was  only  5.4  inches,  while  in  the  adjacent  ungrazed  stand  (EK-234),  aspen 
suckers  were  significantly  taller;  mean  = 50.9  inches  (Student’s  t test,  t = 4.64,  p< 
.001 ).  Unless  burned  aspen  stands  are  protected  from  grazing  for  a number  of 
years,  livestock  use  can  endanger  clonal  survival. 


59 


Figure  27.  Allotment  boundary  comparison.  Stag  Mountain  Allotment  is  to  the 
left  of  the  fence,  while  the  Deeth  Allotment  is  on  the  right.  Aspen  stand  EK-234 
(photo  right)  experienced  a major  regeneration  event  during  the  early  1980’s 
when  the  Connors  Basin  pasture  was  temporarily  destocked.  McIntyre  pasture 
(photo  left)  was  never  destocked  and  EK-233  did  not  regenerate  during  the  early 
1980’s.  The  entire  area  was  burned  by  the  Stag  Mountain  fire  in  2001 . Print 
from  color  slide  (Appendix  C - - No.  338)  by  Charles  E.  Kay;  August  31 , 2002. 


60 


Figure  28.  Aspen  stand  EK-234,  Connors  Basin  Field,  Deeth  Allotment.  This  is 
a close  up  of  the  aspen  stand  seen  in  Figure  27.  EK-234  experienced  a major 
regeneration  event  during  the  early  1980’s  when  this  pasture  was  temporarily 
destocked  due  to  permittee  bankruptcy.  The  site  was  then  swept  by  wildfire  in 

2001 . The  black  objects  near  the  bottom  of  the  aspen  stand  are  trespass  cattle. 
Print  from  color  slide  (Appendix  C - - No.  339)  by  Charles  E.  Kay;  August  31 , 

2002. 


61 


Figure  29.  Aspen  stand  EK-233,  McIntyre  Field,  Stag  Mountain  Allotment.  This 
is  a close  up  of  the  aspen  stand  seen  in  Figure  27.  Unlike  its  neighbor  on  the 
adjacent  allotment  (EK-234),  EK-233  did  not  regenerate  during  the  1980’s.  After 
this  stand  was  swept  by  wildfire  in  2001 , it  was  legally  grazed  by  cattle  in  2002. 
When  measured,  sucker  density  was  1 1 , 1 22  stems  per  acre  with  a mean  height 
of  5.4  inches.  Shown  is  the  belt  transect’s  centerline  (yellow  tape).  Survey  pole 
(6  ft.)  for  scale.  Print  from  color  slide  (Appendix  C - - No.  346)  by  Charles  E. 

Kay;  August  31, 2002. 


62 


Figure  30.  Aspen  stand  EK-234,  Connors  Basin  Field,  Deeth  Allotment.  This  is 
a close  up  of  the  aspen  stand  seen  in  Figures  27  and  28.  When  measured, 
aspen  sucker  density  was  49,900  stems  per  acre  with  a mean  height  of  50.9 
inches  - - compare  this  with  Figure  29.  Print  from  color  slide  (Appendix  C - - No. 
354)  by  Charles  E.  Kay;  August  31 , 2002. 


63 


Pole  Creek  Tributary  - Indian  Creek  Field,  Devils  Gate  Allotment 

Aspen  along  this  tributary  of  Pole  Creek  (Section  1,  township  39N,  Range 
58E)  was  visually  evaluated,  but  no  stands  were  measured  (Appendix  A).  The 
Isolation  fire  burned  this  area  in  2001  and  cattle  were  present  when  the  site  was 
visited.  Most  aspen  stands  in  this  area  appear  to  have  been  on  a downward 
trend  prior  to  the  2001  fire,  and  post-fire  sprouting  appears  limited  (Figure  31 ). 
This  suggests  that  additional  protection  is  warranted. 


64 


Figure  31 . Aspen  along  an  unnamed  tributary  to  Pole  Creek,  Indian  Creek  Field, 
Devils  Gate  Allotment.  Aspen  in  this  area  appears  to  have  been  on  a downward 
trend  prior  to  the  2001  Isolation  fire,  and  post-burn  aspen  suckering  has  been 
limited.  Print  from  color  slide  (Appendix  C - - No.  581 ) by  Charles  E.  Kay; 
September  3,  2002. 


65 


Pole  Creek  Allotment 

Aspen  along  Pole  Creek  (Section  12,  Township  39N,  Range  58E)  was 
visually  evaluated,  but  no  stands  were  measured  (Appendix  A).  Most  of  these 
aspen  stands  appear  to  have  experienced  a major  regeneration  event  about  20 
years  prior  to  being  burned  by  the  2001  Isolation  fire  (Figures  32  to  34).  This 
area  was  not  grazed  by  livestock  in  2002  and  most  stand  have  produced  an 
abundance  of  new  suckers.  Additional  years  of  non-use  will  be  required, 
however,  if  an  adequate  crop  of  aspen  saplings  is  to  mature. 


66 


Figure  32.  Aspen  along  Pole  Creek  on  the  Pole  Creek  Allotment.  This  area  was 
burned  by  the  Isolation  fire  in  2001 . Judging  by  the  size  of  the  fire-killed  trees, 
most  aspen  stands  experienced  a major  regeneration  event  approximately  20 
years  prior  to  being  burned.  Print  from  color  slide  (Appendix  C - - No.  587)  by 
Charles  E.  Kay;  September  3,  2002. 


67 


Figure  33.  Close  up  of  a burned  aspen  stand  along  Pole  Creek.  This  area  was 
burned  by  the  Isolation  fire  in  2001  and  most  aspen  stands  resprouted  at  various 
stem  densities.  Print  from  color  slide  (Appendix  C - - No.  590)  by  Charles  E. 

Kay;  September  3,  2002. 


68 


Figure  34.  An  old  beaver  dam  on  Pole  Creek,  Pole  Creek  Allotment.  Judging  by 
old  stumps  and  other  evidence,  much  of  the  area  along  the  stream  in  this 
photograph  was  once  a fully  stocked  aspen  stand.  At  some  point  in  the  past, 
however,  the  site  was  colonized  by  beaver,  who  felled  the  mature  aspen  for  food 
and  dam  building  materials.  The  cut  aspen  likely  resprouted,  but  the  new 
suckers  were  then  repeatedly  browsed  by  livestock,  until  large  portions  of  the 
stand  were  eliminated.  Print  from  color  slide  (Appendix  C - - No.  592)  by  Charles 
E.  Kay;  September  3,  2002. 


69 


Tuscarora  Mountains 

I was  directed  by  BLM  to  only  measure  aspen  stands  found  on  federal 
lands  in  the  Tuscarora  Mountains,  which  included  primarily  the  Spanish  Ranch 
and  Squaw  Valley  Allotments.  This  limited  the  number  of  aspen  stands  that  I 
was  able  to  sample  because  most  aspen  in  the  Tuscarora  Mountains  occurs  on 
private  property.  I did,  however,  visually  evaluate  aspen  throughout  the  range. 
This  included  Nelson  Creek,  Berry  Creek,  Lewis  Creek,  Toe  Jam  Creek,  Rock 
Creek,  upper  McCann  Creek,  upper  Big  Cottonwood  Canyon,  Dry  Creek,  and 
upper  Red  Cow  Creek  (Appendix  A).  Aspen  stands  were  measured  on  upper 
Red  Cow  Creek,  upper  Dry  Creek,  upper  McCann  Creek,  and  upper  Toe  Jam 
Creek  - - EK-253  to  EK-262  (Appendix  A;  Appendix  B;  Appendix  C - - slides  602 
to  881). 

Most  aspen  stands  within  the  study  area  (see  Appendix  A)  have 
regenerated  over  the  last  20  years  and  generally  are  in  good  ecological 
condition,  except  around  springs  or  other  areas  where  cattle  concentrate  (Tables 
11  to  13;  Figures  35  to  42).  According  to  BLM  records,  these  allotments  were 
partially  destocked  during  the  1980’s  when  the  Ellison  Ranch  cattle  herd  was 
under  brucellosis  quarantine  (Ken  Wilkinson,  personal  communication,  2003). 
Little  mule  deer  sign  was  observed  in  this  mountain  range,  but  some  elk  sign  was 
seen  in  upper  Toe  Jam  and  Rock  Creeks.  According  to  BLM,  a small  elk  herd  is 
found  in  that  area.  This  is  the  only  mountain  range  visited  in  the  three  years  of 
this  study  in  which  elk  sign  was  observed  (Kay  2001a,  2002). 


Table  11.  Aspen  stand  parameters  in  the  Tuscarora  Mountains. 


70 


a> 

E 

3 


TD 

C 

CO 

•¥-» 

W 


co 

cm 

■ 

* 

UJ 


CO 

CM 

i 

* 

LU 


O 

CD 

CM 

i 

* 

LU 


05 

in 

CM 

I 

* 

UJ 


00 

m 

CM 

I 

* 

UJ 


h- 

m 

CM 

I 

X. 

UJ 


CO 

m 

CM 

■ 

* 

UJ 


m 

m 

CM 

■ 

X. 

UJ 


M- 

m 

CM 

■ 

* 

UJ 


CO 

m 

CM 

I 

* 

UJ 


o z UJ 
CM  o O 
Tt-  m 


o Z UJ 
CM  o O 
tj-  m 


o Z UJ 
CM  o O 
M-  m 


CM 


CO 


Z UJ 

o a> 

M-  M- 


Z UJ 

O 05 

Tf  M- 


^ z 


UJ 

O CT> 


m 


CM 


CM 


CM 


Z UJ 
o o 
tj-  m 


Z UJ 
o o 
•M-  m 


Z UJ 
o o 
tt  m 


z uj 

o o 
m 


o 

TS 

<o 

w 


UJ 

o 

o 


o 

m 


CO  00 

"X  ^ 

m r^. 

m m 


UJ  Z 
o o 
o m 
co  o 
m 
in  r~- 
m m 

M" 

UJ  z 
o o 
m m 
h~  r- 
'Cf 

in  t'- 
m m 

■'t 

UJ  z 
o o 
o m 
i-  co 
o CM 
m co 
m m 

M" 

UJ 
o 
o 

CO 
oo  CO 


o 

o 


M-  OO 

m m 

UJ  Z 
o o 
o o 

CO  T- 
Is-  CO 
M-  CO 

m m 

M" 

Ul  Z 
o o 
o o 

05  CO 
CO  o 
m oo 
m m 
m- 

Ul  Z 
o o 
o m 

CD  CO 

co  m 
m r~- 
m m 


o 

m 


ul 
o 
o 
00 
m 
m r»- 
m m 

M- 

Ul  z 

gg 

CO  CM 

m m 
m t'- 
m m 


O 

CM 

CO 


O 

O 


o 

o 

r^- 


o 

CM 

r'- 

co 


o 

o 

CM 

I''- 


O 

CO 

O 

OO 


O 

0O 

O) 

h- 


Q. 

c 

!c 

o 

</) 

05 

3 

1 

CD 

c: 

5 

CO 

> 

o 

co 

H 

05 

h- 

IX 

D 

UJ 

Ul 

CO 


CO 


CO 


UJ 


Ul 

CO 


CO 


■G 

& 

V) 

< 


m 

CO 


m 

CM 


m 


o 

M- 

o 

CM 


m 

CM 


m 


& 

o 

CO 


o 

o 

$ 

o 

r- 


o 

o 

x 

o 

05 


O 

o 

s 

o 

o 

CM 


o 

CO 

% 

o 


o 

0 

1 

CO 


CM  00  T-  S if 

Tf  CO  if  CO  CO 

s ® m t- 


o o o 


oo  -o-  m 
CO  O CO 
05  00  CO 


M" 

CO 


o o o 


00 

05 

CM 

o m 

C'- 

^ — 

O 

co 

CM 

00 

•sf 

CO 

CM 

CO 

o o o 


o 

CO 


o 

CM 


in  m t-  o M- 

o t—  r — co 

o o OO  t- 

T-  CO 


g-  N 'f  O N 
O CO  CO  CO 
OO  S T- 


CM  O O 


o o o 


o 

z 

m 

o 

o 

O 

o 

cm  in 

m 

T— 

CM  O O 

o 

eg 

CM 

CM 

CO 

•*-  o 

co 

o 

m 

^ — 

CO 

M-  O 

co 

CM 

X 

T— 

CM  1- 

o 

o 


o 

co 

s 

o 


miMC'-M-T— 
O 00  O CO  o 
O O "M-  T-  CM 
T—  (O  T- 


o o o 


O 

Ul 

o 

o 

o 

eg 

m o oo 

CM 

(0 

T“ 

05 

OO  M CO 

OO 

^ — 

CO  CO  CM 

f'- 

X 

T— 

CO  T- 

o o o 


o 

o 


o 

y 

o 

m 


m o i — t—  o O) 

CM  M-  -M-  T-  co 

(O  h-  CM  CO  if 
1-  CM  CM 


CM  O O 


1/5 

T3 

^>5 

<15 

N 

</) 

■a 

C 

CO 

"♦-* 

C/) 


I e 

05  C 

St 

O)  CJ) 
05  'sz 

a: 


§ 

TO, 

to 

05 

it; 

</> 

c 

05 

•o 

E 

05 

■*—» 

CO 


X 

CD 

a 

E x x 

CM  00  CD 

V ° Q 

v .E  .E 

C V oo 

• I 

CO  CM  M- 


CD 


00 

A 


8. 

3 

°*  * £■  ^ 
o C 05  0) 
— CO  JC  05 

05  o w Q 

CL 


o 

z 


o 

5 

o 

o 

o 

CO 

00 

CM  O 00 

05  O O 

o 

co 

CO 

CO 

o 

o 

h- 

M- 

O CO 

z 

o 

Z 

5 

T— 

T — 

^ — 

eg 

05 

'if  CM 

r- 

1 

1 

X 

CM 

§ 

o 

o 

05 

10 

05 

>- 


«0 

05 

>- 


1/5 

05 

>- 


05 

CD 

£ 


Pellet  groups  per  2x30  m (6.6  x 98  ft.)  belt  transect.  **Water  in  or  near  stand.  NA=Not  applicable. 


71 


Table  12.  Age  and  diameter  of  aspen  in  the  Tuscarora  Mountains.  R=stem  with  heart  rot 

that  could  not  be  aged.  Stems  less  than  3 inches  were  cut  and  aged  at  ground  level 


Stand  Number 

Stem  Diameter  (inches)/Age  (yrs) 

EK-253 

1/9.  2/10.  2/12.  2/12.  2/14.  2/20,  3/20.  3/21.  3/19.  3/20,  3/21,  4/22,  4/20,  4/21,  5/24, 
14/76,  15/75,  16/80 

EK-254 

EK-255 

EK-256 

EK-257 

EK-258 

EK-259 

EK-260 

EK-261 

EK-262 

1/8,  3/9,  2/10,  2/10,  2/12,  3/19,  3/18,  3/20,4/21,  4/24,  8/75,  9/77,  11/78 

1/12,  2/12,  2/14,  3/14,  3/19,  4/20,  5/21,  8/R,  8/68,  8/70 

1/9,  2/12,  2/14,  4/19,  5/21,  5/20,  6/23,  8/45,  9/49 

1/8,  2/8,  2/10,  2/11,  2/12,  2/12,  3/13,  5/15,  14/105,  23/107,  24/R 

1/8,  1/8,  2/10,  2/4,  2/12,  3/12,  3/11,  4/18,  14/108,  15/107 

1/8,  2/9,  2/10,  2/12,  3/12,  3/12,  3/13,  4/14,  12/85,  13/84 

1/6,  1/9,  1/8,  2/10,  2/12,  2/13,  2/15,  3/14,  3/14,  3/14,  3/14,  8/83,  9/85 

1/6,  1/10,  3/14,  3/14,  3/14,  8/84,  9/85 

1/8,  1/8,  2/10,  2/12,  3/14,  3/14,  3/14,  3/13,  4/14,  5/19,  10/62,  10/65,  11/68 

72 


CD 

O 

(0 


</> 

c 

CO 

tz 

3 

o 


co 

o 

L— 

CO 

o 

CO 

3 


0> 

-C 


V) 

T3 

C 

CO 

CO 


CD 

CL 

10 

CD 


c 

q 

CO 

o 

Q. 

E 


co 

CD 

o 

CD 

CL 

co 

o 

2 

CD 

TJ 

C 

U 

CO 

0) 

-Q 

CO 


CM 

CO 

CM 

* 

LU 

CO 

CM 

LU 

O 

CO 

CM 

£ 

LU 

<_ 

CD 

a> 

CO 

> 

CM 

o 

O 

* 

LU 

a. 

o 

c 

CO 

O 

00 

CO 

CM 

c 

1 

* 

ID 

LU 

O 

ID 

D. 

h- 

T3 

lO 

C. 

CM 

CO 

1 

* 

ID 

LU 

Xl 

E 

3 

Z 

CD 

co 

■o 

CM 

| 

c 

CO 

LU 

CO 

CO 

co 

CM 

* 

LU 

•M- 

CO 

CM 

* 

LU 

CO 

CO 

CM 

* 

UJ 

v> 

CD 

O 

8. 

CO 

o 

■o- 


O Lf)  I— 
CO 


o in 

CO 


CO  • CO 


CO  CO  I— 


CO 

CO 


O 

CM 


CO  co 


■ CO 


CO  CO 
CM 


CO  CO  ' CO  CO  co  |—|— 


CO 


CO  co  1— 
t-  CO 


O O I— 


CO  CO 


CO 


CO 


O O co 

CO  T- 


O CO 
CO  T- 


o 

CM 


CO 


O O 


o o i— 


co  o i— 


co 

CO 


o I- 


o 

CM 


o 

CO 


o 

CO 


o 

CO 


co  O (— 


o o 

CM  i- 


w 

E 

xi 


t XI 
ID  CO 


</> 

E 

XI 

ID  _ 
o>  O t_ 

CQ  q)  <J) 

r u ID  W JC  -S 

t — co  on 

O .S’  SZ  3 

rnnoc: 


CD  ^ 

XI  C 
£ ro 
o 

C 3 5 
CO  O S 


* 

o 


ID 

XJ 

ID 

O 

> 

ID 

to 


co 

ID 

8 

CO 

l_ 

CD 


tn 

■e 

o 


8 

£ £ o 

CU  33  O 

od  Lj  a: 


73 


Figure  35.  A typical  aspen  stand  along  Nelson  Creek.  Most  aspen  in  this  and 
other  drainages  in  the  Tuscarora  Mountains  successfully  regenerated  over  the 
last  20  years,  when  cattle  management  was  voluntarily  changed,  but  not  before. 
Print  from  color  slide  (Appendix  C - - No.  628)  by  Charles  E.  Kay;  September  13, 
2002. 


74 


Figure  36.  Typical  aspen  stands  along  Lewis  Creek.  Most  aspen  in  this  and 
other  drainages  in  the  Tuscarora  Mountains  successfully  regenerated  over  the 
last  20  years,  when  cattle  management  was  voluntarily  changed,  but  not  before. 
Viewed  Southeast.  Print  from  color  slide  (Appendix  C - - No.  649)  by  Charles  E. 
Kay;  September  13,  2002. 


75 


Figure  37.  Aspen  in  upper  Toe  Jam  Creek  on  a mixture  of  public  and  private 
lands.  Most  aspen  in  this  and  other  drainages  in  the  Tuscarora  Mountains 
successfully  regenerated  over  the  last  20  years,  where  cattle  management  was 
voluntarily  changed,  but  not  before.  Viewed  north-northeast.  Print  from  color 
slide  (Appendix  C - - No  670)  by  Charles  E.  Kay;  September  13,  2002. 


76 


Figure  38.  Close  up  of  aspen  in  upper  Toe  Jam  Creek.  Note  the  abundance  of 
aspen  saplings.  Print  from  color  slide  (Appendix  C - - No.  694)  by  Charles  E. 
Kay;  September  13,  2002. 


77 


Figure  39.  Aspen  stand  EK-253  in  upper  Toe  Jam  Creek.  Aspen  saplings  in  this 
stand  had  a density  of  over  5,500  stems  per  acre  and  most  were  between  10  and 
20  years  of  age  (Tables  1 1 and  12).  The  larger  trees  were  80  years  old.  Red 
and  white  survey  pole  (6  ft.)  for  scale.  Print  from  color  slide  (Appendix  C - - No 
724)  by  Charles  E.  Kay;  September  14,  2002. 


78 


ills 


Figure  40.  Aspen  in  upper  Rock  Creek  on  a mixture  of  public  and  private  lands. 
Most  aspen  in  this  and  other  drainages  in  the  Tuscarora  Mountains  successfully 
regenerated  over  the  last  20  years,  when  cattle  management  was  voluntarily 
changed,  but  not  before.  Print  from  color  slide  (Appendix  C - - No.  747)  by 
Charles  E.  Kay;  September  14,  2002. 


Figure  41.  Aspen  in  upper  Big  Cottonwood  Canyon.  Most  aspen  in  this  and 
other  drainages  in  the  Tuscarora  Mountains  successfully  regenerated  over  the 
last  20  years,  when  cattle  management  was  voluntarily  changed,  but  not  before. 
Print  from  color  slide  (Appendix  C - - No.  780)  by  Charles  E.  Kay;  September  14, 
2002. 


80 


Figure  42.  Close  up  of  a heavily  grazed  aspen  stand  along  upper  Dry  Creek  in 
the  Tuscarora  Mountains.  Where  cattle  concentrate,  however,  aspen  stands 
have  not  successfully  regenerated.  Print  from  color  slide  (Appendix  C - - No. 
819)  by  Charles  E.  Kay;  September  15,  2002. 


81 


Adobe  Mountains 

I was  directed  by  BLM  to  only  measure  aspen  stands  found  on 
public  lands  in  the  Adobe  Mountains.  I did,  however,  visually  evaluate  aspen  and 
range  conditions  throughout  the  northern  Adobes  (Appendix  A;  Appendix  C - - 
slides  882  to  1 ,056;  EK-263  to  EK-275).  Most  aspen  stands  in  the  Adobe 
Mountains  have  not  regenerated  in  nearly  100  years  and  are  in  very  poor 
ecological  condition  (Tables  14  to  16;  Figures  43  to  47).  Where  aspen  has  been 
protected  inside  exclosures,  however,  it  has  regenerated  without  fire  or  other 
disturbance  and  is  in  much  better  ecological  condition  (Tables  14  to  16;  Figures 
49  to  51).  Inside  exclosures,  measured  aspen  stands  (n=3)  had  a mean 
understory  canopy  cover  of  60%  grasses  and  forbs,  with  only  2%  bare  soil  (Table 
16).  While  grazed  aspen  stands  (n=10)  had  a mean  understory  composition  of 
34%  bare  soil  and  only  20%  grasses  and  forbs  (Table  16;  Figure  48).  Riparian 
areas  were  also  in  exceedingly  poor  condition  (Beever  and  Brussard  2000) 
throughout  this  mountain  range  (Figures  52  to  55)  and  active  soil  erosion  was 
widespread  (Figures  56  and  57).  Sheet  erosion  was  especially  common  in  Long 
Canyon  and  Coal  Mine  Basin.  Most  of  the  Adobe  Mountains  are  in  a joint-use 
allotment  grazed  by  both  domestic  sheep  and  cattle. 


Table  14.  Aspen  stand  parameters  in  the  Adobe  Mountains. 


82 


a> 

-Q 

E 


■a 

c 

ro 

W 


e-- 

CM 

■ 

* 

LU 


CO 

e- 

CM 

i 

* 

UJ 


CM 

e~ 

CM 

I 

UJ 


r- 

CM 

I 

UJ 


o 

C'- 

CM 

I 

* 

UJ 


05 

CO 

CM 

I 

* 

UJ 


oo 

CO 

CM 

i 

* 

UJ 


in  Z UJ 
cm  r^.  10 
co  m 


o z UJ 

« N CO 
CO  m 


Z UJ 
r-~  m 
co  m 


co 


Z UJ 
e-  CO 
co  m 


c -c 


v>  a> 

I c 

u/  O TO 

who: 


o 

TS 

a) 


uj  z 

O O 

m o 
co  m- 
r-~  co 

o M- 

co  m 

M" 

UJ  z 

O O 
m in 


e-- 

e-- 

o 


cn 

m 

M- 


co  in 

M’ 

UJ  Z 
O O 

o o 

CO  CO 
C"  CM 

o in 
co  in 
•o- 

UJ  Z 
o o 
o o 
CO  r- 
00  CO 

o m 
co  m 
m- 


o 

m 

co 

co 


o 

m 

m 

co 


o 

in 

05 

co 


o 

m 

o 

e^ 


UJ 

(/) 

UJ 


UJ 

CO 


t-  m 

i—  m 

co  m 


co  m 

•M- 


2 

E 

D 


c 

o 

‘•H 

CD 

> 

a> 

UJ 


ts 

& 

</> 

< 


m 

CM 


o 

co 


UJ  “ 


o 

co 

i 

o 

CM 


O 

in 

■ 

in 

CM 


z 

UJ 

UJ 

Z 

o 

z 

o 

T — 

00 

CO 

o 

o 

o 

CO 

CO 

in 

o 

o 

o> 

o 

co 

o 

CD 

CM 

o 

o 

T — 

CO 

CO 

m 

M" 

oo 

z 

UJ 

UJ 

z 

O 

O 

CM 

oo 

co 

o 

o 

in 

CO 

CO 

m 

o 

o 

co 

(/) 

CM 

CM 

co 

T— 

CO 

T — 

in 

CO 

m 

M" 

CO 

z 

UJ 

UJ 

Z 

o 

UJ 

O 

CO 

00 

co 

o 

o 

00 

v 

CO 

in 

m 

o 

co 

m 

co 

CO 

CO 

0) 

CL 

o 

CO 


o 

o 

X 

o 

co 


3 

o 

I"- 


o 

co 

§ 

o 

05 


O 

CM 

X 

o 

CM 


O 

O 

X 

o 

e'- 


en 

co 

x 

o 

CO 


X 

o 

CM 


o o o o o 


o o o 


e'- 

z 

UJ 

UJ  Z 

o 

UJ 

o 

o 

en 

CO 

oo 

CO 

o o 

o 

T — 

05 

CM 

co 

m 

m o 

CM 

1 

X 

1 

* 

UJ 

e-  cm 

CM  M- 

CO 

in 

m 

T — 

t-  m 
co  in 

M- 

co 

Z 

UJ 

UJ  Z 

o 

£ 

o 

o 

CO 

v- 

oo 

co 

o o 

m 

e- 

CO 

CM 

1 

UJ 

co 

in 

o o 
cm  la- 
in 05 

t—  m 

co 

co 

z 

• 

o 

co 

X 

o 

CO 

co  m 

o- 

m 

Z 

UJ 

UJ  z 

o 

£ 

o 

o 

CD 

T — 

oo 

co 

o o 

o 

CD 

05 

CM 

1 

* 

UJ 

co 

m 

o o 
cm  m 
m 05 
t-  m 
co  m 

CO 

CO 

z 

C5 

M- 

X 

o 

e- 

■m- 

•M- 

CO 

Z 

UJ 

UJ  Z 

o 

<: 

O 

o 

eo 

T— 

oo 

co 

o o 

o 

05 

CM 

1 

UJ 

co 

m 

o 00 
m 05 
CO  <35 
■t-  m 
co  m 

CO 

CO 

1 

O 

CM 

X 

o 

CO 

-<* 

CO 

CM 

Z 

UJ 

UJ  Z 

o 

£ 

O 

o 

CD 

00 

co 

o o 

m 

CM 

CO 

CM 

cO 

m 

o o 

•*— 

z 

1 

m 

X 

1 

* 

UJ 

<35  e— 
CO  o 

5T-  CO 

to 

1 

z 

o 

CM 

10 

T3 

>\ 

a> 

N 

'&) 

■a 

tz 

CD 

CO 


o 

oo 


o 

o 


o 

CM 


O 

CM 


O 

O 


O 

O 


|£ 
2 3 

05  C 
C = 

O)  05 

I 2 


o 

o 


o 

o 


o 

o 


o 

o 


o 

o 


CO 


o 

o 


< 

z 


T3 

a> 


o 

i_ 

JO 

£ 

05 

u 

3 

CO 


05COCOCMN 
OO  CO  O O CO 
it  in  co  m- 


co  o o o e'- 
er) co 

CM 


moo 


05  O O 


CO 

r- 

CM 


o o o o 


o o 


cm  o o o h- 
e»  co 

o 


co  e-  o o in 
m-  e-  *- 
m t- 


O 05  OO  O M- 

00  O CD  CO 

CO  OO  CM  T- 


m oo  rt  o r^ 

O CO  CO  CO 
O O r- 


00  CM  M-  r- 
CM  05  M- 
CM  T- 


o o o o o 


CO  o o 


e-  o o 


o o o 


o o 


co  m o 


o o o o o 


t-  e~-  e~-  o o 

M-  OO  CO 

m o e- 

T—  Tf 


OO  N O 


05  00  O 
t-  CM 


o o o 


05 

L 

o 

^D 

C/5 

05 

•e 

t t ) 
c 

05 

TO 

E 

05 

w 


X 

CO 

a 


c 
CM 

V 

V 

d m- 

CO  CM 


X X 
DO  CD 

a 


x 

ao 

Q 


= •—  c 


oo 

A 


« 

V) 

Cl 

3 

O 

® ® 8-  ^ 
(D  JS  05  05 
= <D  r a) 
(I)  O (0  Q 
CL 


t/5 

05 

> 


t/5 

05 

> 


05 

>- 


CO 

05 

>- 


to 

05 

> 


to 

05 

>- 


to 

05 

>- 


to 

05 

>- 


to 

05 

>- 


to 

05 

>- 


L 

05 

CD 

$ 


Pellet  groups  per  2x30  m (6.6  x 98  ft.)  belt  transect.  **Water  in  or  near  stand.  NA=Not  applicable. 


Table  14.  Aspen  stand  parameters  in  the  Adobe  Mountains. 


83 


a> 

n 

E 

3 

Z 

■a 

cz 

CD 

CO 


CO 

00  Z UJ 

UJ  z 

o 

UJ 

o 

o 

r- 

T~  h-  CO 

O O 

CO 

CO 

cn 

CO 

CM 

i 

* 

LU 

CO  co 

o o 

CO  CO 
OO  o 
o m 
CO  CO 
M' 

o> 

CO 

co 

CO 

X 

o 

OO 

o 

o 


o 

o 


CT>  I"- 
r-  CO 

oo 

co 


o o -m- 
co 


cm  o o 


in 

TD 

>; 

0) 


c 

o 


CD 


c 

sz 

o 

'</> 

(D 

o 

to 

in  cd 
1 C 

2 

V* 

CD 

> 

T3 

CD 

o 

CD 

CL 

"O 

C 

C 

CD 

O) 

CD 

o TO 

t 

CD 

(/) 

O 

CO 
1 

CD 

CO 

i-  a: 

3 

UJ 

< 

CO 

CO 

o: 

TO 

<D 

c 


T3 

CD 

</) 

£ 

O 

-Q 

£ 

a> 

o 

3 

CO 


cd 

l 

o 

■2- 

cn 

a) 


X 

00 

O 


•3  = I X x 

‘ «ss| 


c/> 

c 

cd 

■o 


_ c v- 

£ CD  « , 

V CO  CM 


E .E  d 


M-  OO 


CO 


oo 

A 


* 

co 

CL 

3 

i?®  §•*. 

ID  C (D  ® 
— CD  j:  CD 
CD  o CO  O 
CL 


CD 

cu 


Pellet  groups  per  2x30  m (6.6  x 98  ft.)  belt  transect.  "Water  in  or  near  stand.  NA=Not  applicable. 


84 


Table  15.  Age  and  diameter  of  aspen  in  the  Adobe  Mountains.  R=stem  with  heart  rot 

that  could  not  be  aged.  Stems  less  than  3 inches  were  cut  and  aged  at  ground  level 


Stand  Number 

Stem  Diameter  (infchesJ/Age  (yfs) 

EK-263 

EK-264 

EK-265 

EK-266 

EK-267 

EK-268 

EK-269 

EK-270 

EK-271 

EK-272 

EK-273 

EK-274 

EK-275 

2/10,  2/10,  2/10,  3/10,  3/10,  3/11,  14/R 

No  live  stems  in  stand 

No  live  stems  in  stand 

No  data  collected  - - see  original  data  sheet 

No  data  collected  - - see  original  data  sheet 

18/109,  20/R  - - see  original  data  sheet 

15/R 

22/100,  23/R,  24/R,  24/103 

17/100 

16/97,  17/R 

1/8,  2/10,  2/11,2/12,  6/32,  7/30,  15/98,  17/R 
No  live  stems  in  stand  - - see  original  data  sheet 
1/8,  2/10,  2/10,  2/10,  2/12,  15/R,  16/95,  17/102 

85 


to 

o 

TO 


tn 

3 

■to 

3 

3 

o 


TO 

13 

O 

•a 

< 

a) 


e/> 

T3 

3 

TO 

tn 

3 

CD 

CL 

tn 

TO 


3 

o 

L— < 

'tn 

o 

CL 

E 

o 

o 

tn 

TO 

O 

TO 

CL 

tn 

£ 

0 

1 

TO 

■a 

3 

3 

CD 

T“* 

TO 

13 

TO 


TO 

> 

O 

O 

>* 

CL 

O 

3 

TO 

O 
-*— < 
3 
TO 
O 

s 

TO 

Q- 

■a 

3 

TO 

L. 

TO 

13 

E 

3 


TO 
3 
TO 
■*— * 

cd 


CM 

f'- 

CM 

i 

iC 

Ui 


CM 

* 

LJJ 


O 

C-~ 

CM 

I 

* 

LU 


a> 

to 

CM 

i 

* 

111 


00 

CD 

CM 

X. 

LU 


r-- 

CD 

CM 

I 

LU 


CO 

CD 

CM 

I 

LU 


CO 

CD 

CM 

I 

* 

LU 


O 

CD 

CM 

i 

LU 


CO 

CD 

CM 

* 

LU 


tn 

TO 

o 

TO 

CL 

CD 


O 1 CO  I— 
CM 


O h-  • H 


o 

CM 


ID 


O I—  I—  ID  I—  O ■ 1 1 

CO  T— 


O I—  ID  m ID  • I— 


in 


o 

CM 


CO 


CO 


o in  1 o 1 ■ ' 1 m 


ID  ID  ' O 1 I—  * ID  O 


CD  ID  | — O | — I — | — 
T—  CO 


o l—  I—  o I—  1 ' ' • 

O'  T- 


CD  1 ID  i ' i ■ i ■ 
CM 


O 

CO 


co 

CO 


o 

CM 


O 

CM 


O ID  ID 
O 


O CO  ID 
ID 


O CD  I— 
O 


ID  CO  (— 
CM 


■ Cl  < 


l-oh 


CO 


CO 


CD 


CD 


t-  H 


i i i i i 


O 

CO 


CO 

o 


O H H 
co 


o 

•o 


§ H l_ 


ID  O 
CM 


-3 
tn 

E 

-C  -3 

S s 

E 13 

13  TO 

TO  c_ 

S’!  TO 

« e s 

.21  3 3 

cq  o a: 


-3 

tn 

&& 
C JO  TO  TO 
Jr  TO  .3  13 
TO  t-  o TO 
-P  C TO  O 
5 TO  > 
O <U  O C_ 
3 i-  J3  TO 

CD  O O CD 


O TO 
= tn 
5 o 

«>  a : 


tn 

TO 

tn 

tn 

CD 

O 


o 

tn 

-e 

tn 

E 

L- 

TO 

J«C 

O 

o 

CO 

a 

o 

u_ 

CQ 

_i 

UL 

86 


0) 

o 

CO 


C/5 

c 

CO 
■* — 1 
c 
3 

o 


CD 

-Q 

O 

T3 

< 

CD 


c/> 

T3 

c 

CO 

t? 

c 

CD 

Cl 

C/5 

CO 


c 
O 
V- < 
*</5 
O 
CL 

E 

8 

C/5 

CD 

O 

CD 

CL 

CO 

O 


CD 
T 3 
C 

3 

CO 


0) 

-O 

CO 


CD 

> 

o 

O 

>* 

Q. 

O 

c 

CO 

O 

c 

CD 

2 

CD 

CL 

■a 

c 

CO 

CD 

.Q 

E 

3 

z 

•D 

C 

TO 

w 


in 

CM 

* 

uu 


It 

CM 

* 

UJ 


CO 

l''- 

CM 

I 

UJ 


co 

CD 

O 

8. 

w 


o 

CO 


o n in 


• m in 


m 


o m m 

CM 


m 


m i—  • m 1 m 'mm 


o 

CM 


m 


o m 

CM 


o m 

CM 


in  in  h 


sz 

co 

E 


-Q 

-Q 

CO 


CO 

E 

n 

cd  — 
m E CD 

,2>  3 3 

m o a: 


CO 

. I ?£■ 

co  a>  a) 

~ (0  JC  o 
® *-  O 0) 
■Q  c <u  o 
| a)  ^ > 

o CD  ° c_ 

C I-  J=  CD 

WOOW 


O CD 

— co 

■>  ° 

$ DC 


co 

CD 

g 

co 

L_ 

O 


co 

€ 

o 

u_ 


8 

2 ® o 
CO  ts  o 
CO  CL 


87 


Figure  43.  Aspen  stand  EK-264  in  the  Adobe  Mountains.  The  area  around  this 
spring  in  Long  Canyon  was  once  a fully-stocked  aspen  stand.  Repeated  use  by 
domestic  sheep  and  cattle,  however,  has  now  eliminated  this  aspen  clone  (Table 
14).  Print  from  color  slide  (Appendix  C - - No.  91 1 ) by  Charles  E.  Kay; 
September  18,  2002. 


88 


Figure  44.  Close  up  aspen  stand  EK-264  in  the  Adobe  Mountains.  Repeated 
use  by  domestic  sheep  and  cattle  has  eliminated  this  aspen  clone  (Table  16). 
Print  from  color  slide  (Appendix  C - - No.  902)  by  Charles  E.  Kay;  September  18, 
2002. 


89 


Figure  45.  Aspen  stand  EK-270  in  the  Adobe  Mountains.  This  and  other  stands 
in  the  Adobe  Mountains  are  in  very  poor  ecological  condition  and  have  not 
regenerated  in  more  than  100  years  due  to  repeated  browsing  by  livestock.  Print 
from  color  slide  (Appendix  C - - No.  989)  by  Charles  E.  Kay;  September  19, 

2002. 


90 


Figure  46.  Aspen  stand  EK-272  in  the  Adobe  Mountains.  This  and  other  stands 
in  the  Adobe  Mountains  are  in  very  poor  ecological  condition  and  have  not 
regenerated  in  nearly  100  years  due  to  repeated  browsing  by  livestock.  Print 
from  color  slide  (Appendix  C - - No.  1019)  by  Charles  E.  Kay;  September  19 
2002. 


91 


Figure  47.  A de  facto  exclosure  in  aspen  stand  EK-272  in  the  Adobe  Mountains. 
Except  where  physically  protected  by  downed  trees  (Kay  2001a,  2002;  Ripple 
and  Larsen  2001)  or  tall,  unpalatable  shrubs  (Vera  2000:132-162),  aspen  in  this 
stand  has  not  been  able  to  produce  new  stems  greater  than  6 feet  in  height 
because  all  the  suckers  have  been  repeatedly  browsed.  Print  from  color  slide 
(Appendix  C - - No.  1021)  by  Charles  E.  Kay;  September  19,  2002. 


92 


Figure  48.  Aspen  inside  Long  Canyon  Exclosure  number  one.  Viewed  northeast 
to  aspen  inside  Long  Canyon  Exclosure  number  one,  which  was  constructed  in 
1 986  - - note  the  fenceline  contrast  nearest  the  camera.  In  the  Adobe 
Mountains,  grazed  aspen  stands  had  a mean  understory  composition  of  34% 
bare  soil  and  only  20%  grasses  and  forbs,  while  exclosure  - protected  aspen 
stands  had  an  average  understory  species  composition  of  60%  grasses  and 
forbs,  with  only  2%  bare  soil  (Table  16).  Print  from  color  slide  (Appendix  C - - 
No.  888)  by  Charles  E.  Kay;  September  18,  2002. 


93 


Figure  49.  Close  up  of  aspen  inside  Long  Canyon  Exclosure  number  one. 

Aspen  (EK-263)  inside  this  and  all  other  Adobe  Mountain  exclosures  successfully 
regenerated  without  fire  or  other  disturbance  once  livestock  were  excluded.  The 
saplings  in  this  photograph  have  had  their  lower  branches  grazed-off  by  livestock 
some  time  after  they  regenerated,  as  cattle  have  breached  this  exclosure  in 
years  past.  This  exclosure  was  built  in  1986.  Print  from  color  slide  (Appendix  C - 
- No  887)  by  Charles  E.  Kay;  September  18,  2002. 


94 


Figure  50.  Aspen  inside  Coal  Mine  Canyon  Exclosure  number  two.  Aspen 
inside  this  and  all  other  Adobe  Mountain  exclosures  successfully  regenerated 
without  fire  or  other  disturbance  once  livestock  were  excluded  This  exclosure 
was  constructed  in  1985.  Print  from  color  slide  (Appendix  C - - No.  957)  by 
Charles  E.  Kay;  September  18,  2002. 


95 


Figure  51.  Aspen  inside  Coal  Mine  Canyon  Exclosure  number  three.  Aspen 
(EK-268)  inside  this  and  all  other  Adobe  Mountain  exclosures  successfully 
regenerated  once  livestock  were  excluded.  This  exlosure  was  built  in  1985. 

Print  from  color  slide  (Appendix  C - - No.  968)  by  Charles  E.  Kay;  September  18, 
2002. 


96 


Figure  52.  Typical  riparian  conditions  in  the  Adobe  Mountains.  Most  riparian 
areas  in  the  Adobe  Mountains  are  in  very  poor  ecological  condition  (Borman  et  al 
1999,  Beever  and  Brussard  2000,  Clary  and  Leininger  2000).  Print  from  color 
slide  (Appendix  C - - No.  980)  by  Charles  E.  Kay;  September  19,  2002. 


97 


Figure  53.  Fenceline  contrast  at  Coal  Mine  Canyon  Exclosure  number  one. 
Viewed  south  along  the  eastern  edge  of  Coal  Mine  Canyon  Exclosure  number 
one.  Note  the  contrasting  condition  of  the  riparian  area.  Livestock  are  excluded 
from  the  area  to  the  right  of  the  fence.  This  exlosure  was  built  in  1 986.  Print 
from  color  slide  (Appendix  C - - No.  948)  by  Charles  E.  Kay;  September  18, 
2002. 


98 


Figure  54.  Ungrazed  riparian  area  inside  Coal  Mine  Canyon  Exclosure  number 
one.  Compare  this  with  Figure  55.  Print  from  color  slide  (Appendix  C - - No. 
950)  by  Charles  E.  Kay;  September  18,  2002. 


99 


Figure  55.  Grazed  riparian  area  below  Coal  Mine  Canyon  Exclosure  number 
one.  Compare  this  with  Figure  54.  Print  from  color  slide  (Appendix  C - - No. 
949)  by  Charles  E.  Kay;  September  18,  2002. 


100 


Figure  56.  Soil  erosion  in  the  Adobe  Mountains.  Note  the  extensive  hillside 
erosion  above  Wildcat  Spring.  Sheet  erosion  is  common  in  Long  Canyon  and 
Coal  Mine  Basin.  Print  from  color  slide  (Appendix  C - - No.  882)  by  Charles  E. 
Kay;  September  18,  2002. 


101 


Figure  57.  Close-up  of  sheet  erosion  in  Long  Canyon.  Hillside  erosion  is 
common  in  Long  Canyon  and  Coal  Mine  Basin.  This  is  an  indication  of  poor 
range  conditions  (Borman  et  al.  1999,  Beever  and  Brussard  2000,  Clary  and 
Leininger  2000).  Print  from  color  slide  (Appendix  C - - No.  937)  by  Charles  E 
Kay;  September  18,  2002. 


102 


DISCUSSION  AND  CONCLUSIONS 

Many  aspen  stands  in  north-central  Nevada  are  in  poor  condition  and 
have  not  successfully  regenerated  in  nearly  100  years.  During  the  present  study, 
limited  elk  sign  was  observed  only  in  the  Tuscarora  Mountains,  so  elk  have 
generally  not  contributed  to  the  decline  of  aspen  on  BLM  lands  in  north-central 
Nevada.  In  other  areas  of  the  West,  however,  elk  have  had  and  are  having 
serious,  negative  effects  on  aspen  communities  (Kay  1985,  1997a,  1997c, 

2001b,  2001c;  White  et  al.  1998a,  1998b,  2003;  Ripple  and  Larsen  2000;  White 
2001).  If  elk  colonize  additional  areas  in  north-central  Nevada  or  are  transplanted 
onto  BLM  lands,  it  is  highly  likely  that  those  animals  would  have  a negative 
impact  on  aspen  (Wall  et  al.  2001 :697).  In  Nevada’s  Jarbridge  Mountains,  for 
instance,  Beck  and  Peek  (2001 ) reported  that  summer  elk  use  was  concentrated 
in  aspen. 

Forest  succession  is  also  not  a problem  in  the  aspen  stands  that  were 
studied,  as  conifers  had  not  invaded  any  of  the  communities  that  were  measured. 
Aside  from  Pinyon  (Pinus  spp.).  and  Juniper  (Juniperus  spp.),  conifers  are 
generally  absent  from  the  mountain  ranges  that  were  visited  in  north-central 
Nevada.  There  is  also  no  evidence  that  normal  plant  succession  favors 
sagebrush  over  aspen,  as  claimed  by  some  (Schenbeck  and  Dahlem  1977). 
Where  it  has  been  protected  from  grazing,  aspen  in  central  Nevada  has  not 
succeeded  to  sagebrush,  but  instead  has  maintained  its  position  in  the 
vegetation  association  (Kay  2001a,  2002).  Other  exclosure  studies  have  found 


103 


that  protected  aspen  stands  have  actually  expanded  and  killed-out  sagebrush 
(Kay  1990,  2001a,  2001b;  Kay  and  Bartos  2000).  Thus,  there  are  no  data  to 
support  the  contention  that  the  decline  of  aspen  in  north-central  Nevada  is  due  to 
normal  successional  processes. 

Exclosure  studies  also  suggest  that  climate  has  had  little  impact  on  aspen 
in  central  Nevada  (Kay  and  Bartos  2000;  Kay  2001a,  2002).  In  fact,  data  from 
across  the  West  has  failed  to  demonstrate  a relationship  between  climatic 
variation  and  a corresponding  decline  in  aspen  (DeByle  and  Winokur  1985; 

Baker  et  al.  1997;  Kay  1997a,  2001a,  2001b;  White  et  al.  1998a,  1998b,  2003; 
Kay  and  Bartos  2000;  Ripple  and  Larsen  2000;  White  2001). 

It  is  also  commonly  assumed  that  aspen  has  declined  due  to  fire 
suppression  by  federal  and  state  land  management  agencies  (Houston  1973, 
1982;  Despain  et  al.  1986;  Romme  et  al.  1995;  Wall  etal.  2001).  While  fire 
usually  has  a positive  effect  on  aspen  by  eliminating  invading  conifers  and 
stimulating  sucker  production,  the  condition  and  trend  of  aspen  communities  in 
north-central  Nevada  are  not,  in  general,  related  to  an  absence  of  fire.  If  only 
burned  aspen  stands  were  capable  of  producing  new  stems  greater  than  6 ft  tall, 
then  aspen  inside  fenced  plots  or  aspen  protected  by  fallen  trees,  should  not  be 
able  to  successfully  regenerate.  In  all  cases  where  aspen  was  protected  from 
ungulate  herbivory  in  Nevada,  however,  it  has  successfully  regenerated  without 
fire  or  other  disturbance  (Kay  2001a,  2002),  and  the  same  is  true  throughout  the 
West  (White  et  al.  1998b,  Kay  and  Bartos  2000,  Kay  2001b,  White  2001).  Thus, 
while  fire  can  benefit  the  species,  aspen  has  not  declined  solely  due  to  fire 


104 

suppression.  This  leaves  ungulate  herbivory  as  the  main  reason  aspen  has 
declined  in  central  Nevada,  and  across  the  West  (Kay  1997a,  Kay  and  Bartos 
2000,  Ripple  and  Larsen  2000,  White  2001). 

Data  from  exclosures  on  Stag  Mountain  and  in  the  Adobe  Range,  as  well 
as  other  areas  (Kay  2001a,  2002),  indicate  that  ungulate  herbivory  has  had  a 
major  influence  on  aspen  stem  dynamics  and  understory  species  composition  in 
north-central  Nevada.  Most  herbivory  was  attributable  to  domestic  livestock,  not 
wildlife.  Of  the  1 ,309  pellet  groups  previously  recorded  on  aspen  belt  transects 
in  north-central  Nevada,  710  (54.2%)  were  from  cattle,  596  (45.5%)  from 
domestic  sheep,  and  3 (0.2%)  from  mule  deer  (Kay  2001a,  2002).  While  in  the 
present  study,  of  the  325  pellet  groups  recorded  on  aspen  plots,  234  (72.0%) 
were  from  cattle,  90  (27.7%)  from  domestic  sheep,  and  1 (0.3%)  from  mule  deer. 
Similarly,  aspen  regenerated  throughout  central  Nevada  wherever  it  was 
protected  by  the  interlocking  branches  of  fallen  trees  (Ripple  and  Larsen  2001), 
by  steep  cut  banks,  or  dense  brush  (Vera  2000:132-162;  Kay  2001a,  2002). 
Aspen  also  regenerated  on  central  Nevada  ranges  where  livestock  use  was 
reduced  (Kay  2001a,  2002),  such  as  Connors  Basin  Field  on  Stag  Mountain. 

The  fact  that  aspen  stands  on  steep  slopes  far  from  water  are  generally  in 
better  condition  than  stands  on  more  gentle  slopes  near  water,  is  also  related  to 
livestock  grazing  patterns  (Kay  2001a,  2002).  According  to  other  studies 
(Holechek  1988:11-12),  slopes  of  11-30%  reduce  cattle  grazing  by  30%,  while 
slopes  of  31-60%  receive  60%  less  use  by  cattle  than  areas  with  0-10%  slope. 

On  sites  with  slopes  over  60%,  cattle  use  is  essentially  zero.  Similarly,  areas  1-2 


105 


miles  from  water  receive  50%  less  use  by  cattle  than  sites  closer  to  water,  while 
areas  more  than  two  miles  from  water  are  seldom  used  by  cattle  (Holechek 
1988:11-12). 

I have  now  personally  measured  or  otherwise  evaluated  nearly  60  aspen 
exclosures  in  the  western  U.S.  and  Canada  (Kay  1990,  2001a,  2001b,  2002;  Kay 
et  al.  1999;  Kay  and  Bartos  2000),  and  in  all  cases  where  aspen  has  been 
protected,  it  successfully  regenerated  and  formed  multi-aged  stands  without  fire 
or  other  disturbance.  The  single,  stem-aged  stands  found  in  central  Nevada  and 
throughout  the  West  are  not  a biological  attribute  of  aspen,  but  a result  of 
excessive  ungulate  herbivory.  In  other  areas  I have  worked,  the  problem  has 
been  too  many  elk  (Kay  1997a,  1997c,  2001b,  2001c;  White  et  al.  1998b)  or  too 
many  mule  deer  (Kay  and  Bartos  2000).  In  central  Nevada,  however,  domestic 
livestock  are  the  predominate  ungulate  herbivore. 

Recently,  the  Bureau  of  Land  Management,  the  U.S.  Forest  Service,  and 
other  agencies,  have  transplanted  beaver  to  restore  damaged  riparian  areas 
(Munther  1982,  1983;  Smith  1980,  1983a,  1983b;  Kay  1994;  McKinstry  and 
Anderson  1997;  Albert  and  Trimble  2000;  Lukas  2000;  McKinstry  et  al.  2001). 

The  Forest  Service,  for  instance,  has  used  beaver  to  improve  wetlands  in 
Montana  and  Oregon,  while  BLM  established  beaver-transplant  demonstration 
projects  on  degraded  streams  in  southwest  Wyoming  (Johnson  1984,  Bergstrom 
1985).  Moreover,  other  researchers  have  demonstrated  that  beaver  is  a 
“keystone  species”  that  completely  alters  the  hydrology,  energy  flow,  and  nutrient 
cycling  of  aquatic  systems  (Naiman  and  Melillo  1984;  Parker  et  al.  1985;  Naiman 


106 


et  al.  1986,  1988;  Platts  and  Onishuk  1988;  Johnston  and  Naiman  1987,  1990; 
Smith  et  al.  1991;  Pollock  et  al.  1995;  McCall  et  al.  1996).  Beaver  dams  impound 
water  and  trap  sediments  that  raise  the  water  table,  increase  the  wetted 
perimeter,  and  allow  the  extension  of  riparian  communities  into  former  upland 
sites  (Smith  1980,  Apple  1983).  In  addition,  beaver  dams  regulate  stream  flow 
by  storing  water,  reducing  peak  or  flood  flow,  and  augmenting  low  flows  during 
summer  (Smith  1983b).  During  dry  periods,  30  to  60  percent  of  the  water  in  a 
stream  system  can  be  held  in  beaver  ponds  (Smith  1983a).  By  trapping  silt  over 
thousands  of  years,  beaver  dams  created  many  of  the  West’s  fertile  valleys  (Ives 
1942).  Munther  (1982,  1983)  reported  that  a typical  creek  without  beaver 
furnishes  only  about  two  to  four  acres  of  riparian  habitat  per  stream  mile  in  the 
northern  Rockies;  but  with  beaver  activity,  that  area  can  be  expanded  to  twenty- 
four  acres  per  mile. 

Beaver  need  tall  willows  or  aspen  as  food  and  dam-building  materials. 
Aspen  and  willows  cut  by  beaver  normally  resprout  (Kindschy  1985,  1980)  and  in 
turn  provide  additional  beaver  food.  Once  the  mature  aspen  trees  or  tall  willows 
are  cut,  however,  the  new  suckers  are  entirely  within  reach  of  browsing  animals 
(Kay  1994).  By  preventing  aspen  and  willows  from  growing  into  sizeable  plants, 
ungulate  herbivory  can  eliminate  beaver  foods  and  eventually  the  beaver 
themselves. 

Flook  (1964)  and  Nietvelt  (2001)  reported  that  high  elk  numbers  negatively 
affected  beaver  through  interspecific  competition  for  willows  and  aspen  in 
Canada’s  Banff  and  Jasper  National  Parks.  In  Yellowstone  National  Park, 


107 


beaver  are  now  ecologically  extinct  over  large  areas  because  the  combined 
action  of  beaver  and  excessive  elk  herbivory  has  eliminated  aspen  and  willows 
(Kay  1990,  1994,  1997d,  1997e;  Chadde  and  Kay  1991;  Kay  and  Walker  1997). 
Bergerud  and  Manuel  (1968),  as  well  as  Collins  (1976)  noted  that  high  moose 
(AJces  alces)  densities  had  a similar  negative  effect  on  beaver  in  Newfoundland 
and  in  Wyoming’s  Jackson  Hole.  While  others  have  reported  that  heavy  grazing 
by  domestic  livestock  reduced  woody  vegetation,  which,  in  turn,  negatively 
impacted  beaver  populations  and  riparian  systems.  (Platts  et  al.  1983;  Smith  and 
Flake  1983;  Dieter  1987;  Dieter  and  McCabe  1989a,  1989b).  This  is  what  has 
happened  on  the  Elko  District  (Kay  2002).  Aspen  + beaver  + repeated  livestock 
use  eliminated  both  aspen  and  beaver,  which  subsequently  caused  streams  to 
downcut  and  erode.  So,  while  beaver  generally  have  a positive  effect  on 
riparian  communities,  beaver  plus  excessive  herbivory  have  the  opposite  result. 

Similarly,  fire  can  also  have  a negative  effect  on  aspen.  That  is  to  say, 
burned  aspen  communities  will  not  successfully  regenerate  if  ungulate  herbivory 
is  excessive  (Bartos  and  Mueggler  1981;  White  et  al  1998b,  2003;  Kay  2001c). 
Cattle  grazing  on  Stag  Mountain  (Table  3)  clearly  has  had  a negative  impact  on 
aspen  sucker  height  growth  after  fire,  and  if  allowed  to  continue,  may  eventually 
eliminate  those  stands.  This  is  why  aspen  stands  must  be  rested  for  several 
years  following  fire.  If  the  underlying  problem  is  ungulate  herbivory,  beaver  will 
not  improve  riparian  conditions,  and  fire  will  not  successfully  regenerate  aspen. 
Burning  highly  degraded  aspen  stands  should  not  be  attempted  until  ungulate 
herbivory  problems  are  solved. 


108 


MANAGEMENT  RECOMMENDATIONS 

To  reverse  the  decline  of  aspen  on  BLM  administered  lands  in  north- 
central  Nevada  it  will  be  necessary  to  more  closely  manage  livestock. 

Depending  on  site-specific  conditions,  it  may  be  necessary  to  fence  some  aspen 
stands,  if  those  clones  are  to  survive.  In  other  areas,  season-of-use  changes 
may  be  sufficient  to  restore  aspen  (Kay  2001a).  Year-long  or  season-long 
grazing  is  particularly  detrimental  to  aspen,  while  early-season  or  dormant- 
season  use  may  allow  aspen  to  successfully  regenerate.  That  is  to  say,  the 
timing  of  grazing  can  be  more  important  than  the  intensity  (Borman  et  al.  1999). 

As  many  aspen  stands  in  north-central  Nevada  are  located  in  riparian 
settings,  it  may  also  be  necessary  to  fence  those  areas  to  exclude  livestock  and 
to  pipe  water  to  sites  some  distance  from  aspen  - - of  all  the  springs,  seeps,  and 
other  water  sources  observed  in  north-central  Nevada,  few  were  developed  and 
most  were  heavily  grazed  by  livestock  (Clary  and  Leininger  2000;  Kay  2001a, 
2002).  AUM  reductions  may  also  be  necessary  on  some  allotments.  In 
evaluating  which  measures  to  implement  on  what  stands,  distance  to  or  from 
water,  and  the  degree  of  slope  are  the  two  most  important  risk  factors  (Holechek 
1988).  Aspen  near  water  is  at  greater  risk  than  more  distant  stands  and  aspen 
on  gentle  topography  is  more  at  risk  than  stands  on  steep  slopes  - - all  other 
factors  being  equal  - - except  on  domestic  sheep  allotments,  where  upper- 
elevation  aspen  stands  near  bedding  areas  may  also  be  at  risk  (Kay  2002). 

Since  there  is  relatively  little  aspen  on  BLM  lands  in  north-central  Nevada  and 


109 


because  there  are  no  known,  practical  ways  of  reestablishing  aspen  (Shepperd 
and  Battaglia  2002:92),  the  demise  of  even  a single  aspen  clone  should  not  be 
an  option,  especially  since  so  much  has  been  lost  already,  at  least  in  some 
areas. 

It  is  also  strongly  recommended  that  BLM  establish  permanent  vegetation 
sampling  plots  in  aspen  communities  throughout  north-central  Nevada  to 
evaluate  any  management  actions  the  agency  might  take.  One  of  the  most  cost 
effective  ways  would  be  to  establish  a series  of  permanent  photopoints  (Magill 
1989;  Hart  and  Laycock  1996;  Hall  2002a,  2002b).  As  there  are  so  few  long- 
term, aspen-containing  exclosures  on  BLM  lands  in  the  Elko  District,  all  existing 
aspen  exclosures  should  be  retained,  and  new  ones  constructed  as  needed. 

Just  because  aspen  inside  an  exclosure  has  regenerated  that  does  not  mean  the 
exclosure  should  automatically  be  removed,  since  the  fenced  area  is  still  an 
important  range  reference  area  (Laycock  1975). 

If  fire  is  used  to  restore  aspen  communities,  it  may  be  necessary  to  rest 
those  areas  for  1 to  2 years  prior  to  treatment  to  allow  fine  fuels  to  accumulate 
(Brown  and  Simmerman  1986).  Pure  aspen  stands  are  very  difficult  to  burn  and 
will  usually  burn  only  early  in  the  spring  prior  to  leaf-out  or  late  in  the  fall  after 
leaf-drop  (Brown  and  Simmerman  1 986).  If  aspen  is  burned  or  felled  by  beaver, 
it  will  also  be  necessary  to  rest  those  areas  for  a minimum  of  3 to  5 years  to  allow 
the  new  suckers  to  grow  beyond  the  reach  of  grazing  animals;  i.e.  6 to  8 feet  tall. 
In  some  cases,  this  could  be  accomplished  with  temporary  electric  fencing. 
Whatever  is  done,  however,  BLM  needs  to  be  more  vigilant  in  its  monitoring.  All 


110 


fenced  areas  and  exclosures  should  be  checked  at  least  yearly  to  insure  that 
management  goals  are  being  met.  BLM  may  also  wish  to  reconsider  its  policy  of 
putting  gates  in  some  exclosures  to  prevent  those  areas  from  being  used  as 
holding  pastures.  Alternatively,  BLM  could  decide  to  lock  all  the  gates  on  its 
exclosures  and  provide  keys  to  the  grazing  permittees  so  that  any  cattle,  which 
inadvertently  enter  the  exclosures,  could  quickly  be  removed.  Grazing  permits 
should  specifically  state  that  exclosures  are  not  to  be  grazed  by  livestock. 

If  beaver  colonize  any  new  areas,  those  stream  reaches  will  need  to  be 
fenced  or  aspen  will  likely  be  eliminated,  as  it  has  in  the  past,  by  repeated 
livestock  browsing.  Unlike  fire,  which  kills  all  the  mature  trees  in  a single  event, 
and  thereby  stimulates  large-scale  suckering  events,  beaver  cut  mature  aspen 
over  a period  of  years.  Thus,  aspen  suckering  and  aspen  sucker  densities  are 
less,  and  aspen  can  more  easily  be  eliminated  by  repeated  livestock  use. 

Stag  Mountain 

Deeth  Allotment  - Connors  Basin  Field 

To  maintain  the  pre-fire  abundance  and  distribution  of  aspen  in  this  pasture, 
it  is  my  recommendation  that  the  entire  area  be  rested  until  the  majority  of  new 
aspen  stems  in  all  stands  are  well  beyond  the  reach  of  cattle.  This  likely  will  require 
2 to  3 years  additional  rest. 


Ill 


Deeth  Allotment  - Hanks  Creek  Basin  Field 

Maintain  the  existing  exclosures;  West  Hanks  Creek,  East  Hanks  Creek, 
Antelope  Basin;  and  monitor  to  insure  that  cattle  are,  in  fact,  excluded.  Other 
aspen  stands  in  this  pasture  may  also  need  to  be  fenced,  especially  those  where 
livestock  tend  to  concentrate.  That  is  to  say,  all  stands  without  aspen  saplings  will 
likely  need  to  be  fenced  if  those  clones  are  to  survive. 

Stag  Mountain  Allotment  - McIntyre  Field 

Aspen  in  this  pasture  is  in  very  poor  ecological  condition  and  season  of  use 
changes  or  AUM  reductions  will  likely  be  necessary  if  aspen  is  to  survive.  If  this  is 
not  done,  than  many  aspen  stands  will  need  to  be  fenced  or  they  will  be  eliminated. 
The  voluntary  reduction  of  domestic  sheep  use  that  has  occurred  in  this  pasture 
over  the  last  few  years  appears  to  have  helped  some  aspen  stands  and  should  be 
made  permanent. 

Cheveller  Exclosure 

Maintain  the  existing  exclosure  and  monitor  to  insure  that  cattle  are  in  fact, 
excluded.  BLM  may  also  wish  to  experiment  in  re-establishing  aspen  along 
sections  of  the  stream  where  aspen  was  eliminated  by  the  combined  action  of 


112 

beaver  and  livestock  prior  to  livestock  exclusion. 

Pole  Creek  and  Pole  Creek  Tributary 

To  maintain  the  pre-fire  abundance  and  distribution  of  aspen  in  these 
pastures,  it  is  my  recommendation  that  the  entire  area  be  rested  until  the  majority  of 
new  aspen  stems  in  all  stands  is  well  beyond  the  reach  of  cattle.  This  may  require 
2 to  3 years  additional  rest. 


Tuscarora  Mountains 

Aspen  in  the  Tuscarora  Mountains  is  generally  in  good  ecological  condition. 
A few  stands,  however,  receive  heavy  livestock  use  and  those  areas  will  have  to  be 
fenced  if  those  clones  are  to  survive.  The  growing  elk  population  in  this  mountain 
range  should  be  closely  monitored  and  herd  objectives  set  that  will  not  adversely 
impact  aspen. 


Adobe  Mountains 

Aspen  in  the  Adobe  Mountains  is  in  very  poor  ecological  condition  and  many 
clones  will  be  lost  if  the  situation  is  not  corrected  in  the  near  future.  Riparian  areas 
also  appear  to  be  in  exceedingly  poor  condition  and  active  soil  erosion  is 
widespread.  In  all  my  years  afield,  I have  not  seen  such  extensive  sheet  erosion, 
except  in  textbooks  or  national  parks  (Kay  1997e).  Thus,  this  entire  allotment  may 


113 


have  to  be  closed  for  several  years  if  the  range  is  to  recover,  but  I will  leave  that 
decision  to  BLM  riparian  and  soil  experts,  who  I recommend  conduct  an  emergency 
analysis  of  the  entire  area,  especially  Long  Canyon  and  Coal  Mine  Basin.  In 
addition,  all  existing  exclosures  should  be  maintained  and  monitored  to  insure  that 
livestock  are,  in  fact,  excluded.  If  the  allotment  is  not  closed  or  if  AUM  numbers  are 
not  seriously  reduced,  most  aspen  stands  will  need  to  be  fenced  if  they  are  to 
survive. 


114 


LITERATURE  CITED 

Albert,  S.,  and  T.  Trimble.  2000.  Beavers  are  partners  in  riparian  restoration  on 
the  Zuni  Indian  Reservation.  Ecological  Restoration  18:87-92. 

Apple,  L.L.  1983.  The  use  of  beavers  in  riparian/aquatic  habitat  restoration  in  a 
cold  desert  gully-cut  stream  system:  A case  history.  Proceedings  of  the 
American  Fisheries  Society  18:29-35. 

Baker,  F.S.  1918.  Aspen  reproduction  in  relation  to  management.  Journal  of 
Forestry  16:389-398. 

Baker,  F.S.  1925.  Aspen  in  the  central  Rocky  Mountain  region.  U.S. 
Department  of  Agriculture  Bulletin  No.  1291.  47  pp. 

Baker,  W.L.,  J.  A.  Monroe,  and  A.E.  Hessl.  1997.  The  effects  of  elk  on  aspen  in 
the  winter  range  in  Rocky  Mountain  National  Park.  Ecography  20:155- 
165 

Baida,  R.P.  1975.  Vegetation  structure  and  breeding  bird  diversity.  Pages  59- 
80  in  Smith,  D.R.,  ed.  Symposium  on  management  of  forest  and  range 
habitats  for  nongame  birds.  U.S.  Forest  Service  General  Technical 
Report  WO-1 . 

Bartos,  D.L.,  and  R.B.  Campbell,  Jr.  1998.  Decline  of  quaking  aspen  in  the 
interior  west  - - examples  from  Utah.  Rangelands  20:17-24. 

Bartos,  D.L.,  and  W.F.  Mueggler.  1979.  Influence  of  fire  on  vegetation 

production  in  the  aspen  ecosystem  in  western  Wyoming.  Pages  75-78  in 
Boyce,  M S.  and  L.D.  Hayden-Wing,  eds.  North  American  elk:  Ecology, 


115 


behavior  and  management.  University  of  Wyoming,  Laramie,  WY.  294 
PP- 

Bartos,  D.L.,  and  W.F.  Mueggler.  1981.  Early  succession  in  aspen  communities 
following  fires  in  western  Wyoming.  Journal  of  Range  Management 
34:315-318. 

Bartos,  D.L.,  J.K.  Brown,  and  G.D.  Booth.  1994.  Twelve  years  biomass 
response  in  aspen  communities  following  fire.  Journal  of  Range 
Management  47:79-83. 

Bartos,  D.L.,  W.F.  Mueggler,  and  R.B.  Campbell  Jr.  1991.  Regeneration  of 
aspen  by  suckering  on  burned  sites  in  western  Wyoming.  U.S.  Forest 
Service  Research  Paper  INT-448.  10  pp. 

Beck,  J.L.,  and  J.M.  Peek.  2001.  Jarbridge  cooperative  elk  herd  carrying 

capacity  study  - - 1999  annual  report:  Preliminary  estimates  of  1999  elk 
summer  range  carrying  capacity.  Idaho  Bureau  of  Land  Management 
Technical  Bulletin  No.  01-3.  32  pp. 

Beever,  E.A.,  and  P.F.  Brussard.  2000.  Examining  ecological  consequences  of 
feral  horse  grazing  using  exclosures.  Western  North  American  Naturalist 
60:236-254. 

Bergerud,  A.T.,  and  F.  Manuel.  1968.  Moose  damage  to  balsam  fir-white  birch 
forests  in  central  Newfoundland.  Journal  of  Wildlife  Management  32:729- 
746. 

Bergstrom,  D.  1985.  Beavers:  Biologists  “rediscover”  a natural  resource. 
Forestry  Research  West  (Oct.):  1-5. 


116 

Borman,  M.M.,  C.R.  Massingill,  and  E.W.  Elmore.  1999.  Riparian  area 
responses  to  changes  in  management.  Rangelands  21 :3 -7. 

Brown,  J.K.,  and  D.G.  Simmerman.  1986.  Appraisal  of  fuels  and  flammability  in 
western  aspen:  A prescribed  fire  guide.  U.S.  Forest  Service  General 
Technical  Report  INT-205.  48  pp. 

Cartwright,  C.W.,  Jr.,  and  D.P.  Burns.  1994.  Sustaining  our  aspen  heritage  into 
the  twenty-first  century.  U.S.  Forest  Service,  Southwestern  Region.  6 pp. 

Casey,  D.,  and  D.  Hein.  1983.  Effects  of  heavy  browsing  on  a bird  community  in 
deciduous  forest.  Journal  of  Wildlife  Management  47:829-836. 

Chadde,  S.W.,  and  C.E.  Kay.  1991.  Tall  willow  communities  on  Yellowstone's 
northern  range:  A test  of  the  "natural  regulation"  paradigm.  Pages  231- 
264  in  Keiter,  R.R.,  and  M.S.  Boyce,  eds.  The  Greater  Yellowstone 
Ecosystem:  Redefining  American's  wilderness  heritage.  Yale  University 
Press,  New  Haven,  CT.  428  pp. 

Clary,  W.P.,  and  W.C.  Leininger.  2000.  Stubble  height  as  a tool  for 

management  of  riparian  areas.  Journal  of  Range  Management  53:562- 
573. 

Coles,  F.H.  1965.  The  effects  of  big  game  and  cattle  grazing  on  aspen 

regeneration.  M S.  Thesis,  Brigham  Young  University,  Provo,  UT.  72  pp. 

Collins,  T.C.  1976.  Population  characteristics  and  habitat  relationships  of 

beaver,  Castor  canadensis,  in  northwest  Wyoming.  Ph.D.  Dissertation, 
University  of  Wyoming,  Laramie,  WY.  192  pp. 


117 

Daily,  G.C.,  P.R.  Ehrlich,  and  N.M.  Haddad.  1993.  Double  keystone  bird  in  a 
keystone  species  complex.  Proceedings  of  the  National  Academy  of 
Science  90:592-594. 

DeByle,  N.V.,  C.D.  Bevins,  and  W.C.  Fisher.  1987.  Wildfire  occurrence  in  aspen 
in  the  interior  western  United  States.  Western  Journal  of  Applied  Forestry 
2:73-76. 

DeByle,  N.V.,  and  R.P.  Winokur,  eds.  1985.  Aspen:  Ecology  and  management 
in  the  western  United  States.  U.S.  Forest  Service  General  Technical 
Report  RM-1 19.  283  pp. 

Despain,  D.,  D.  Houston,  M.  Meagher,  and  P.  Schullery.  1986.  Wildlife  in 
transition:  Man  and  nature  on  Yellowstone's  northern  range.  Roberts 
Rinehart,  Boulder,  CO.  142  pp. 

Dieter,  C.D.  1987.  Habitat  use  by  beaver  along  the  Big  Sioux  River.  M.S. 
Thesis,  South  Dakota  State  University,  Brookings,  SD.  60  pp. 

Dieter,  C.D.,  and  T.R.  McCabe.  1989a.  Factors  influencing  beaver  lodge-site 
selection  on  a prairie  river.  American  Midland  Naturalist  122:408-411. 

Dieter,  D.D.,  and  T.R.  McCabe.  1989b.  Habitat  use  by  beaver  along  the  Big 

Sioux  River  in  eastern  South  Dakota.  Pages  135-140  in  Gresswell,  R.E., 
B.A.  Barton,  and  J.L.  Kershner,  eds.  Practical  approaches  to  riparian 
management:  An  educational  workshop.  Bureau  of  Land  Management, 
Montana  State  Office  BLM-MT-PT-89-0001-4351.  193  pp. 

Ehrlich,  P.R.,  and  G.C.  Daily.  1993.  Birding  for  fun:  Sapsuckers,  swallows, 
aspen,  and  rot.  American  Birds  47(1):  18-20. 


118 

Endersby,  H.  1999.  The  aspen-mule  deer  link.  Mule  Deer  4(2):  16-1 9. 

Fechner,  G.H.,  and  J.S.  Barrows.  1976.  Aspen  stands  as  wildfire  fuelbreaks. 
Eisenhower  Consortium  Bulletin  4:1-26.  U.S.  Forest  Service  Rocky 
Mountain  Forest  and  Range  Experiment  Station,  Fort  Collins,  CO. 

Finch,  D M.,  and  L.F.  Ruggiero.  1993.  Wildlife  habitats  and  biological  diversity  in 
the  Rocky  Mountains  and  northern  Great  Plains.  Natural  Areas  Journal 
13:191-203. 

Flack,  J.A.D.  1976.  Bird  populations  of  aspen  forests  in  western  North  America. 
Ornithological  Monograph  No.  19.  97  pp. 

Flook,  D.R.  1964.  Range  relationships  of  some  ungulates  native  to  Banff  and 
Jasper  National  Parks,  Alberta.  Pages  119-128  in  D.J.  Crisp,  ed.  Grazing 
in  terrestrial  and  marine  environments.  Blackwell  Press,  Oxford,  UK.  429 
PP- 

Grant,  M C.  1993.  The  trembling  giant.  Discover  14(1 0):82-89. 

Grant,  T.A.,  and  G.B.  Berkey.  1999.  Forest  area  and  avian  diversity  in 

fragmented  aspen  woodland  of  North  Dakota.  Wildlife  Society  Bulletin 
27:904-914. 

Gruell,  G.E.,  and  L.L.  Loope.  1974.  Relationships  among  aspen,  fire  and 
ungulate  browsing  in  Jackson  Hole,  Wyoming.  U.S.  Forest  Service 
Intermountain  Region,  Ogden,  UT.  33  pp. 

Hall,  F.C.  2002a.  Photo  point  monitoring  handbook:  Part  A - - Field  procedures. 
U.S.  Forest  Service  General  Technical  Report  PNW-GTR-526.  48  pp. 


119 

Hall,  F.C.  2002b.  Photo  point  monitoring  handbook:  Part  B - - Concepts  and 
analysis.  U S.  Forest  Service  General  Technical  Report  PNW-GTR-526. 

86  pp. 

Hart,  R.H.,  and  W.A.  Laycock.  1996.  Repeat  photography  on  range  and  forest 
lands  in  the  western  United  States.  Journal  of  Range  Management  49:60- 
67. 

Holechek,  J.L.  1988.  An  approach  for  setting  the  stock  rate.  Rangelands  10: ID- 
14. 

Houston,  D.B.  1973.  Wild  fires  in  northern  Yellowstone  National  Park.  Ecology 
54:1111-1117. 

Houston,  D.B.  1982.  The  northern  Yellowstone  elk:  Ecology  and  management. 

MacMillan  Publishers,  New  York,  NY.  474  pp. 

Ives,  R.L.  1942.  The  beaver-meadow  complex.  Journal  of  Geomorphology 
5:191-203. 

Jelinski,  D.E.,  and  W.M.  Cheliak.  1992.  Genetic  diversity  and  spatial  subdivision 
of  Populus  tremuloides  (Salicaceae)  in  a heterogenous  landscape. 
American  Journal  of  Botany  79:728-736. 

Johns,  B.W.  1993.  The  influence  of  grove  size  on  bird  species  richness  in 
aspen  parklands.  Wilson  Bulletin  105:256-264. 

Johnson,  M. A.  1994.  Changes  in  southwestern  forests:  Stewardship 
implications.  Journal  of  Forestry  92(12):16-19. 

Johnson,  P.  1984.  The  dam  builder  is  at  it  again!  National  Wildlife  (June-July): 


9-15. 


120 

Johnston,  C.A.,  and  R.J.  Naiman.  1987.  Boundary  dynamics  at  the  aquatic- 
terrestrial  interface:  The  influence  of  beaver  and  geomorphology. 
Landscape  Ecology  1:47-57. 

Johnston,  C.A.,  and  R.J.  Naiman.  1990.  The  use  of  a geographic  information 
system  to  analyze  long-term  landscape  alteration  by  beaver.  Landscape 
Ecology  4:5-19. 

Kay,  C.E.  1985.  Aspen  reproduction  in  the  Yellowstone  Park-Jackson  Hole  area 
and  its  relationship  to  the  natural  regulation  of  ungulates.  Pages  131-160 
in  Workman,  G.W.,  ed.  Western  elk  management:  A symposium.  Utah 
State  University,  Logan,  UT.  213  pp. 

Kay,  C.E.  1990.  Yellowstone's  northern  elk  herd:  A critical  evaluation  of  the 
"natural  regulation"  paradigm.  Ph.D.  Dissertation,  Utah  State  University, 
Logan,  UT.  490  pp. 

Kay,  C.E.  1993.  Aspen  seedlings  in  recently  burned  areas  in  Grand  Teton  and 
Yellowstone  National  Parks.  Northwest  Science  67:94-104. 

Kay,  C.E.  1994.  The  impact  of  native  ungulates  and  beaver  on  riparian 
communities  in  the  Intermountain  West.  Natural  Resources  and 
Environmental  Issues  1 :23-44. 

Kay,  C.E.  1997a.  Is  aspen  doomed?  Journal  of  Forestry  95(5):4-11. 

Kay,  C.E.  1997b.  Aspen:  A new  perspective  - - implications  for  park 

management  and  ecological  integrity.  Pages  265-273  in  Harmon,  D.,  ed. 
Marking  protection  work:  Proceedings  of  the  9th  conference  on  research 


121 


and  resource  management  in  parks  and  on  public  lands.  The  George 
Wright  Society,  Hancock,  Ml.  493  pp. 

Kay,  C.E.  1997c.  The  condition  and  trend  of  aspen,  Populus  tremuloides.  in 
Kootenay  and  Yoho  National  Parks:  Implications  for  ecological  integrity. 
Canadian  Field-Naturalist  111:607-616. 

Kay,  C.E.  1997d.  Viewpoint:  Ungulate  herbivory,  willows,  and  political  ecology 
in  Yellowstone.  Journal  of  Range  Management  50:139-145. 

Kay,  C.E.  1997e.  Yellowstone:  Ecological  malpractice  - - photo  excerpts  from  a 
forthcoming  book.  PERC  Reports  15(2):1-40. 

Kay,  C.E.  1999.  Repeat  photography  and  long-term  vegetational  change  on  the 
U.S.  Sheep  Experiment  Station  and  other  rangelands  in  the  Centennial 
Mountains.  Final  report  to  U.S.  Sheep  Experiment  Station,  Dubois,  ID. 

300  pp. 

Kay,  C.E.  2000.  Native  burning  in  western  North  America:  Implications  for 

hardwood  management.  Pages  19-27  in  Yaussy,  D.A.,  ed.  Proceedings: 
Workshop  on  fire,  people,  and  the  central  hardwood  landscape.  U.S. 
Forest  Service  General  Technical  Report  NE-274.  129  pp. 

Kay,  C.E.  2001a.  The  condition  and  trend  of  aspen  communities  on  BLM 
administered  lands  in  central  Nevada  - - Final  report  to  BLM  Battle 
Mountain  Field  Office,  50  Bastian  Road,  Battle  Mountain,  Nevada,  89820. 

1 55  pp  + Appendices. 

Kay,  C.E.  2001b.  Long-term  aspen  exclosures  in  the  Yellowstone  Ecosystem. 
Pages  225-240  in  Shepperd,  W.D.,  D.  Binkley,  D.L.  Bartos,  T.J.  Stohlgren, 


122 

and  L.G.  Eskew,  eds.  Sustaining  aspen  in  western  landscapes.  U.S. 
Forest  Service  Proceedings  RMRS-P-18.  460  pp. 

Kay,  C.E.  2001c.  Evaluation  of  burned  aspen  communities  in  Jackson  Hole, 
Wyoming.  Pages  215-223  in  Shepperd,  W.D.,  D.  Binkley,  D.L.  Bartos, 

T.J.  Stohlgren,  and  L.G.  Eskew,  eds.  Sustaining  aspen  in  western 
landscapes.  U.S.  Forest  Service  Proceedings  RMRS-P-18.  460  pp. 

Kay,  C.E.  2002.  The  condition  and  trend  of  aspen  communities  on  BLM 

administered  lands  in  the  north-central  Nevada  - - with  recommendations 
for  management.  Final  report  to  BLM  Elko  Field  Office,  3900  East  Idaho 
Street,  Elko,  Nevada,  89801.  193  pp.  + Appendices. 

Kay,  C.E.,  C.A.  White,  I.R.  Pengelly,  and  B.  Patton.  1999.  Long-term  ecosystem 
states  and  processes  in  Banff  National  Park  and  the  central  Canadian 
Rockies.  Parks  Canada  Occasional  Paper  No.  9,  Environment  Canada, 
Ottawa,  ON. 

Kay,  C.E.,  and  D.L.  Bartos.  2000.  Ungulate  herbivory  on  Utah  aspen: 

Assessment  of  long-term  exclosures.  Journal  of  Range  Management 
53:145-153. 

Kay,  C.E.,  and  F.H.  Wagner.  1994.  Historic  condition  of  woody  vegetation  on 
Yellowstone's  northern  range:  A critical  test  of  the  "natural  regulation" 
paradigm.  Pages  151-169  in  Despain,  D.G.,  ed.  Plants  and  their 
environments'  - - Proceeding  of  the  first  biennial  scientific  conference  on 
the  Greater  Yellowstone  Ecosystem.  U.S.  National  Park  Service,  Denver, 
CO.  Technical  Report  NPS/NRYELL/NRTR-93/XX.  347  pp. 


123 

Kay,  C.E.,  and  F.H.  Wagner.  1996.  The  response  of  shrub-aspen  to 
Yellowstone's  1988  wildfires:  Implications  for  "natural  regulation" 
management.  Pages  107-1 1 1 in  Greenlee,  J.M.,  ed.  Ecological 
implications  of  fire  in  Greater  Yellowstone:  Proceedings  of  the  second 
biennial  conference  on  the  Greater  Yellowstone  Ecosystem.  International 
Association  of  Wildland  Fire,  Fairfield,  WA.  235  pp. 

Kay,  C.E.,  and  J.W.  Walker.  1997.  A comparison  of  sheep  and  wildlife  grazed 
willow  communities  in  the  Greater  Yellowstone  Ecosystem.  Sheep  and 
Goat  Research  Journal  13:6-14. 

Kennedy,  T.B.,  A.M.  Merenlender,  and  G.L.  Vinyard.  2000.  A comparison  of 
riparian  condition  and  aquatic  invertebrate  community  indices  in  central 
Nevada.  Western  North  American  Naturalist  60:255-272. 

Kindschy,  R.R.  1985.  Response  of  red  willow  to  beaver  use  in  southeastern 
Oregon.  Journal  of  Wildlife  Management  49:26-28. 

Kindschy,  R.R.  1989.  Regrowth  of  willow  following  simulated  beaver  cutting. 
Wildlife  Society  Bulletin  17:290-294. 

Krebill,  R.G.  1972.  Mortality  of  aspen  on  the  Gros  Ventre  elk  winter  range.  U.S. 
Forest  Service  Research  Paper  INT-129.  16  pp. 

Laycock,  W.A.  1975.  Rangeland  reference  areas.  Society  for  Range 
management,  Range  Science  Series  No.  3.  34  pp. 

Loope,  L.L.,  and  G.E.  Gruell.  1973.  The  ecological  role  of  fire  in  the  Jackson 
Hole  area,  northwestern  Wyoming.  Quaternary  Research  3:425-443. 

Lukas,  D.  2000.  Movers  of  the  Earth.  Audubon  102(2):29-33. 


124 

Magill,  A.W.  1989.  Monitoring  environmental  change  with  color  slides.  U.S. 
Forest  Service  General  Technical  Report  PSW-117.  55  pp. 

McCall,  T.C.,  T.P.  Hodgman,  D.R.  Diefenbach,  and  R.B.  Owen,  Jr.,  1996. 

Beaver  populations  and  their  relation  to  wetland  habitat  and  breeding 
waterfowl  in  Maine.  Wetlands  16:163-172. 

McDonough,  W.T.  1979.  Quaking  aspen  seed  germination  and  early  seedling 
growth.  U.S.  Forest  Service  Research  Paper  INT-234.  13  pp. 

McDonough,  W.T.  1985.  Sexual  reproduction,  seeds  and  seedlings.  Pages  25- 
28  in  N.V.  DeByle,  and  R.P.  Winokur,  eds.  Aspen:  Ecology  and 
management  in  the  western  United  States.  U.S.  Forest  Service  General 
Technical  Report  RM-119.  283  pp. 

McKinstry,  M.C.,  P.  Caffrey,  and  S.H.  Anderson.  2001.  The  importance  of 
beaver  to  wetland  habitats  and  waterfowl  in  Wyoming.  Journal  of  the 
American  Water  Resources  Association.  37: 1 571  -1 577. 

McKinstry,  M.C.,  and  S.H.  Anderson.  1997.  Use  of  Beaver  to  improve  riparian 
areas  in  Wyoming.  Pages  128-134  in  Goertler,  C.,  C.  Rumsey,  T.  Bray, 
and  D.  Boysen,  eds.  Wyoming  water  1997:  Applied  research  for 
management  of  Wyoming’s  water  resources.  Wyoming  Water  Research 
Center,  Laramie,  WY. 

Mitton,  J.B.  and  M.C.  Grant.  1996.  Genetic  variation  and  the  natural  history  of 
quaking  aspen.  Bioscience  46:25-31. 

Mueggler,  W.F.  1988.  Aspen  community  types  of  the  Intermountain  region. 

U.S.  Forest  Service  General  Technical  Report  INT-250.  135  pp. 


125 

Mueggler,  W.F.  1989a.  Age  distribution  and  reproduction  of  Intermountain 
aspen  stands.  Western  Journal  of  applied  Forestry  4:41-45. 

Mueggler,  W.F.  1989b.  Status  of  aspen  woodlands  in  the  West.  Pages  32-37  in 
Pendleton,  B.G.,  ed.  Western  raptor  management  symposium  and 
workshop.  National  Wildlife  Federation  Scientific  and  Technical  Series 
No.  12.  Washington,  D.C. 

Munther,  G.L.  1982.  Beaver  management  in  grazed  riparian  ecosystems. 

Pages  234-241  in  Proceedings  of  the  wildlife-livestock  relationships 
symposium.  University  of  Idaho  Forest,  Wildlife  and  Range  Experiment 
Station,  Moscow,  ID. 

Munther,  G.L.  1983.  Integration  of  beaver  into  forest  management.  Paper 
presented  at  Colorado-Wyoming  Chapter  of  the  American  Fisheries 
Society,  Laramie,  WY.  8 pp. 

Naiman,  R.J.,  and  J.M.  Melillo.  1984.  Nitrogen  budget  of  a subarctic  stream 
altered  by  beaver  (Castor  canadensis).  Oecologia  62: 1 50-1 55. 

Naiman,  R.J.,  J.M.  Melillo,  and  J.E.  Hobbie.  1986.  Ecosystem  alteration  of 

boreal  forest  streams  by  beaver  (Castor  canadensis).  Ecology  67:1254- 
1269. 

Naiman,  R.J.,  C.A.  Johnston,  and  J.C.  Kelley.  1988.  Alteration  of  North 
American  streams  by  beaver.  Bioscience  38:753-762. 

Nelson,  J.R.,  and  T.A.  Leege.  1982.  Nutritional  requirements  and  food  habits. 
Pages  323-367  in  Thomas,  J.S.,  and  D.E.  Toweill,  eds.  Elk  of  North 


126 

America:  Ecology  and  management.  Stackpole  Books,  Harrisburg,  PA. 
698  pp. 

Nietvelt,  C.G.  2001.  Herbivorv  interactions  between  beaver  (Castor  Canadensis) 
and  elk  (Cervus  elaphus)  on  willow  (Salix  spp.)  in  Banff  National  Park, 
Alberta.  M.S.  Thesis,  University  of  Alberta,  Edmonton,  AB.  117  pp. 

Oakleaf,  R.F.,  C.  Masser,  and  T.  Nappe.  1983.  Livestock  and  nongame  wildlife. 
Pages  95-102  in  Menke,  J.W.,  ed.  Proceedings  of  the  workshop  on 
livestock  and  wildlife-fisheries  relationships  in  the  Great  Basin.  University 
of  California  Special  Publications  3301.  173  pp. 

Olmsted,  C.E.  1977.  The  effect  of  large  herbivores  on  aspen  in  Rocky  Mountain 
National  Park.  Ph.D.  Dissertation,  University  of  Colorado,  Boulder,  CO. 
136  pp. 

Olmsted,  C.E.  1 979.  The  ecology  of  aspen  with  reference  to  utilization  by  large 
herbivores  in  Rocky  Mountain  National  Park.  Pages  89-97  in  Boyce,  M.S., 
and  L.D.  Hayden-Wing,  eds.  North  American  elk:  Ecology,  behavior,  and 
management.  University  of  Wyoming,  Laramie,  WY.  294  pp. 

Olmsted,  C.E.  1997.  Twenty  years  of  change  in  Rocky  Mountain  National  Park 
winter  range  aspen.  Technical  Report.  Environmental  Studies  Program, 
University  of  Northern  Colorado,  Greeley,  CO.  41  pp. 

Page,  J.L.,  N.  Dodd,  T O.  Osborne,  and  J.A.  Carson.  1978.  The  influence  of 
livestock  grazing  on  non-game  wildlife.  California-Nevada  Wildlife 


1978:159-173. 


127 


Parker,  M.,  F.J.  Wood,  Jr.,  B.H.  Smith,  and  R.G.  Elder.  1985.  Erosional 

downcutting  in  lower  order  ecosystems:  Have  historical  changes  been 
caused  by  removal  of  beaver?  Pages  35-38  in  Johnson,  R.R.,  C.D. 
Ziebell,  D.R.  Patton,  P.F.  Ffolliott,  and  R.H.  Hamre,  eds.  Riparian 
ecosystems  and  their  management:  Reconciling  conflicting  uses.  U.S. 
Forest  Service  General  Technical  Report  RM-120. 

Perala,  D.A.  1990.  Quaking  aspen.  Pages  555-569  in  Burns,  R.M.,  and  B.H. 
Honkala,  eds.  Silvics  of  north  America.  Volume  2.  hardwoods.  U.S. 
Department  of  Agriculture,  Agriculture  Handbook  654. 

Peterson,  E.B.,  and  N.M.  Peterson.  1992.  Ecology,  management  and  use  of 
aspen  and  balsam  poplar  in  the  prairie  provinces,  Canada.  Forestry 
Canada  Northern  Forest  Center  Special  Report  1.  252  pp. 

Peterson,  E.B.,  and  N.M.  Peterson.  1995.  Aspen  managers’  handbook  for 
British  Columbia.  British  Columbia  Ministry  of  Forests  and  Canadian 
Forest  Service.  FRDA  Report  230.  1 10  pp. 

Platts,  W.S.,  and  M.  Onishuk.  1988.  “Good”  beavers,  “bad”  beavers.  Idaho 
Wildlife  41  (2):23-27. 

Platts,  W.S.,  R.L.  Nelson,  0.  Casey,  and  V.  Crispin.  1983.  Riparian-stream 

habitat  conditions  on  Tabor  Creek,  Nevada,  under  grazed  and  ungrazed 
conditions.  Western  Association  of  Fish  and  Wildlife  Agencies  63:162- 
174. 

Pollock,  M.M.,  R.J.  Naiman,  H E.  Erickson,  C.A.  Johnston,  J.  Pastor,  and  G. 
Pinay.  1995.  Beaver  as  engineers:  Influences  on  biotic  and  abiotic 


128 

characteristics  of  drainage  basins.  Pages  117-126  in  Jones,  C.G.,  and 
J.H.  Lawton,  eds.  Linking  species  and  ecosystems.  Chapman  and  Hall, 
new  York,  NY.  387  pp. 

Putman,  R.J.,  P.J.  Edwards,  J.C.E.  Mann,  R.C.  How,  and  S.D.  Hill.  1989. 

Vegetational  and  faunal  changes  in  an  area  of  heavily  grazed  woodland 
following  relief  of  grazing.  Biological  Conservation  47:13-32. 

Ripple,  W.J.,  and  E.J.  Larson.  2000.  Historic  aspen  recruitment,  elk,  and  wolves 
in  northern  Yellowstone  National  Park,  USA.  Biological  Conservation:  In 
press. 

Ripple,  W.J.,  and  E.J.  Larsen.  2001.  The  role  of  postfire  coarse  woody  debris  in 
aspen  regeneration.  Western  Journal  of  Applied  Forestry  16:61-64. 
Romme,  W.H.,  M.G.  Turner,  L.L.  Wallace,  and  J.S.  Walker.  1995.  Aspen,  elk, 
and  fire  in  northern  Yellowstone  National  Park.  Ecology  76:2097-2106. 
Sampson,  A.W.  1919.  Effect  of  grazing  upon  aspen  reproduction.  U.S. 

Department  of  Agriculture  Bulletin  No.  741.  29  pp. 

Schenbeck,  G.L.,  and  E.A.  Dahlem.  1977.  Proposed  management  of  aspen 
habitat  in  northern  Nevada.  California-Nevada  Wildlife  1977:68-74. 

Schier,  G.A.  1975.  Deterioration  of  aspen  clones  in  the  middle  Rocky 
Mountains.  U.S.  Forest  Service  Research  Paper  INT-170.  14  pp. 

Schier,  G.A.,  and  R.B.  Campbell.  1980.  Variation  among  healthy  and 

deteriorating  aspen  clones.  U.S.  Forest  Service  Research  Paper  INT-264. 

12  pp. 


129 

Shepperd,  W.D.  1993.  Initial  growth,  development,  and  clonal  dynamics  of 
regenerated  aspen  in  the  Rocky  Mountains.  U.S.  Forest  Service 
Research  Paper  RM-312. 

Shepperd  W.D.,  and  F.W.  Smith.  1993.  The  role  of  near-surface  lateral  roots  in 
the  life  cycle  of  aspen  in  the  central  Rocky  Mountains.  Forest  Ecology 
and  Management  61:157-170. 

Shepperd,  W.D.,  and  M.A.  Battaglia.  2002.  Ecology,  silviculture,  and 

management  of  Black  Hills  ponderosa  pine.  U.S.  Forest  Service  General 
Technical  Report  RMRS-GTR-97.  112  pp. 

Shepperd,  W.D.,  and  M.L.  Fairweather.  1994.  Impact  of  large  ungulates  in 
restoration  of  aspen  communities  in  a southwestern  ponderosa  pine 
ecosystem.  Pages  344-347  in  Covington,  W.S.,  and  L.F.  DeBano,  eds. 
Sustainable  ecological  systems:  Implementing  an  ecological  approach  to 
land  management.  U.S.  Forest  Service  General  Technical  Report  RM- 
247.  363  pp. 

Smith,  B.H.  1980.  Not  all  beaver  are  bad;  or,  an  ecosystem  approach  to  stream 
habitat  management,  with  possible  software  applications.  Pages  32-36  in 
Proceedings  of  the  15th  annual  meeting  of  the  Colorado-Wyoming  Chapter 
of  the  American  Fisheries  Society. 

Smith,  B.H.  1983a.  Riparian  willow  management:  Its  problems  and  potentials, 
within  the  scope  of  multiple  use  on  public  lands.  Pages  15-20  in 
Proceedings  of  the  Ninth  Wyoming  Shrub  Ecology  Workshop,  Lander, 
Wyoming. 


130 


Smith,  B.H.  1983b.  Restoration  of  riparian  habitats  within  the  BLM-Rock  Springs 
District.  Paper  presented  at  Wildlife  Habitat  Rehabilitation  and 
Reclamation  Symposium.  January  10-1 1.  Salt  Lake  City,  UT.  8 pp. 

Smith,  M.E.,  C.T.  Driscoll,  B.J.  Wyskowski,  C.M.  Brooks,  and  C.C.  Cosentini. 

1991 . Modification  of  stream  ecosystem  structure  and  function  by  beaver 
(Castor  canadensis)  in  the  Adirondack  Mountains,  New  York.  Canadian 
Journal  of  Zoology  69:55-61. 

Smith,  R.L.,  and  L.D.  Flake.  1983.  The  effects  of  grazing  on  forest  regeneration 
along  a prairie  river.  Prairie  Naturalist  15:41-44. 

Stelfox,  J.B.,  ed.  1995.  Relationship  between  stand  age,  stand  structure,  and 
biodiversity  in  aspen  mixedwood  forests  in  Alberta.  Jointly  published  by 
Alberta  Environmental  Centre,  Vegreville,  AB  and  Canadian  Forest 
Service,  Edmonton,  AB.  308  pp. 

Taylor,  D.M.  1986.  Effects  of  cattle  grazing  on  passerine  birds  nesting  in 
riparian  habitat.  Journal  of  Range  Management  39:254-258. 

U.S.  Forest  Service.  1993.  Changing  conditions  in  southwestern  forests  and 

implications  on  land  stewardship.  U.S.  Forest  Service,  Southwest  Region. 

8 pp. 

Vera,  F.W.M.  2000.  Grazing  history  and  forest  ecology.  CABI  Publishing,  New 
York,  NY.  506  pp. 

Wall,  T.G.,  R.F.  Miller,  and  T.J.  Svejcar,  2001.  Juniper  encroachment  into  aspen 
in  the  northwest  Great  Basin.  Journal  of  Range  Management  54:691-698. 


131 

Wallmo,  O.C.,  and  W.L.  Regelin.  1981.  Rocky  mountain  and  intermountain 
habitats.  Part  1.  Food  habits  and  nutrition.  Pages  387-38  in  Wallmo, 
O.C.,  ed.  Mule  and  black-tailed  deer  of  North  America.  University  of 
Nebraska  Press,  Lincoln,  NE.  605  pp. 

Weatherill,  R.G.,  and  L.B.  Keith.  1969.  The  effect  of  livestock  grazing  on  an 

aspen  forest  community.  Alberta  Department  of  Lands  and  Forests,  Fish 
and  Wildlife  Division  Technical  Bulletin  No.  1.  31  pp. 

Weinstein,  J.  1979.  The  condition  and  trend  of  aspen  along  Pacific  Creek  in 
Grand  Teton  National  Park.  Pages  78-82  in  Boyce,  M.S.,  and  L.D. 
Hayden-wing,  eds.  North  American  elk:  Ecology,  behavior  and 
management.  University  of  Wyoming,  Laramie,  WY.  294  pp. 

West,  N.E.,  K.  McDaniel,  E.L.  Smith,  P.T.  Tueller,  and  S.  Leonard.  1994. 

Monitoring  and  interpreting  ecological  integrity  on  arid  and  semi-arid  lands 
of  the  western  United  States.  New  Mexico  Range  Improvement  Task 
Force,  Las  Cruces,  NM.  Report  37.  15  pp. 

Westworth,  D.A.,  and  E.S.  Telfer.  1993.  Summer  and  winter  bird  populations 
associated  with  five  age-classes  of  aspen  forest  in  Alberta.  Canadian 
Journal  of  Forest  Research  23:1830-1836. 

White,  C.A.  2001.  Aspen,  elk,  and  fire  in  the  Canadian  Rocky  Mountains.  Ph.D. 
Dissertation,  University  of  British  Columbia,  Vancouver,  BC.  192  pp. 

White,  C.A.,  C.E.  Kay,  and  M.C.  Feller.  1998a.  Aspen  forest  communities:  A key 
indicator  of  ecological  integrity  in  the  Rocky  Mountains.  Pages  506-517  in 
Munro,  N.W.P.,  and  J.H.M.  Wilison,  eds.  Linking  protected  areas  with 


132 


working  landscapes  conserving  biodiversity.  Science  and  Management  of 
Protected  Areas  Association.  Wolfville,  NS. 

White,  C.A.,  C.E.  Olmsted,  and  C.E.  Kay.  1998b.  Aspen,  elk,  and  fire  in  the 

Rocky  Mountain  national  parks  of  North  America.  Wildlife  Society  Bulletin 
26:449-462. 

White,  C.A.,  M.C.  Feller,  and  S.  Bayley.  2003.  Predation  risk  and  the  functional 
response  of  elk-aspen  herbivory.  Forest  Ecology  and  Management  (in 
press). 

Winternitz,  B.L.  1980.  Birds  in  aspen.  Pages  247-257  in  Degraff,  R.M.,  ed. 

Workshop  proceedings  on  management  of  western  forests  and  grasslands 
for  nongame  birds.  U.S.  Forest  Service  General  Technical  Report  INT-86. 

Young,  J.L.  1973.  Breeding  bird  populations  and  habitat  utilization  in  aspen 
stands  of  upper  Logan  Canyon.  M.S.  Thesis,  Utah  State  University, 

Logan,  UT.  38  pp. 

Young,  J.L.  1977.  Density  and  diversity  responses  of  summer  bird  populations 
to  the  structure  of  aspen  and  spruce-fir  communities  on  the  Wasatch 
Plateau,  Utah.  Ph.D.  Dissertation,  Utah  State  University,  Logan,  UT.  79 


pp. 


APPENDIX  A 


Project  Maps 


by 


Charles  E.  Kay,  Ph.D. 
Wildlife  Management  Services 
480  East  125  North 
Providence,  Utah  84332 
(435)  753-0715 


December  2002 


APPENDIX  A - - PROJECT  MAPS 


The  1:24,000  USGS  topographic  maps  for  this  project  are  grouped  by  drainage 
or  mountain  range.  On  each  map  the  vehicle  access  routes  are  marked  in  purple^H  , 
while  the  routes  accessed  on  foot  are  marked  in  red  The  approximate  location  of 
each  measured  aspen  stand  is  marked  with  an  EK-number  in  black,  while  the  general 
location  of  other  aspen  stands  is  also  marked  in  black,  usually  with  the  letter  A. 


Area 

1:24.000  maps 

Stag  Mountain 

Hanks  Creek,  NE 
Hanks  Creek,  SW 
Hot  Springs  Creek 
Stag  Mountain 

Tuscarora  Mountains 

Big  Cottonwood  Canyon 
Mount  Blitzen 
Red  Cow  Creek 
Toe  Jam  Mountain 

Adobe  Mountains 

Coal  Mine  Basin 
Coal  Mine  Canyon,  SE 
Dinner  Station 
The  Buttes 
The  Narrows 

APPENDIX  B 


Project  Data  Sheets 


by 


Charles  E.  Kay,  Ph.D. 
Wildlife  Management  Services 
480  East  125  North 
Providence,  Utah  84332 
(435)  753-0715 


December  2002 


APPENDIX  B - - PROJECT  DATA  SHEETS 


This  appendix  contains  photocopies  of  the  original  data  sheets  for  each  aspen 
stand  measured  during  this  project  - - see  text  for  details. 


Area 

Aspen  Stands 

Stag  Mountain 

EK-201  to  EK-252 

Tuscarora  Mountains 

EK-253  to  EK-261 

Adobe  Mountains 

EK-262  to  EK-275 

APPENDIX  C 


Project  Color  Slides 


by 


Charles  E.  Kay,  Ph.D. 
Wildlife  Management  Services 
480  East  125  North 
Providence,  Utah  84332 
(435)  753-0715 


December  2002 


APPENDIX  C - - PROJECT  COLOR  SLIDES 


This  appendix  contains  1056  - - 35  mm  color  slides  of  aspen  stands  in  north- 
central  Nevada.  Each  slide  is  individually  labeled  with  the  date,  mountain  range,  and 
drainage,  as  well  as  consecutively  numbered  in  black  ink.  Stand  numbers  have  also 
been  identified  on  each  slide,  where  appropriate.  The  slides  are  presented  in 
consecutive  order  in  archival  quality  plastic  pages  that  each  hold  20  slides.  The  slide 
pages  are  also  consecutively  numbered;  n=53.  The  red  and  white  survey  pole  seen  in 
many  slides  is  6 feet  tall  in  one  foot  segments.