Elk Calves Research Articles

Influences of supplemental feeding on winter elk calf:cow ratios in the southern Greater Yellowstone Ecosystem

Several elk herds in the Greater Yellowstone Ecosystem are fed during winter to alleviate interactions with livestock, reduce damage to stored crops, and to manage for high elk numbers. The effects of supplemental feeding on ungulate population dynamics has rarely been examined, despite the fact that supplemental feeding is partially justified as necessary for maintaining or enhancing population growth rates. We used linear regression to assess how the presence of feedgrounds, snowpack, summer rainfall, indices of grizzly bear density and wolves per elk, elk population trend counts, brucellosis seroprevalence, and survey date were correlated with midwinter calf:cow ratios, a metric correlated with population growth, from 1983–2010 from 12 ecologically similar elk herd units (7 fed and 5 unfed) in Wyoming, USA. Our statistical approach allowed for rigorous tests of the hypotheses that supplemental feeding had positive effects on calf:cow ratios and reduced sensitivity of calf:cow ratios to bottom-up limitation relative to top-down limitation from native predators. Calf:cow ratios generally declined across all herd units over the study period and varied widely among units with feedgrounds. We found no evidence that the presence of feedgrounds had positive effects on midwinter calf:cow ratios in Wyoming. Further, fed elk showed stronger correlations with environmental factors, whereas calf:cow ratios for unfed elk showed stronger correlations with predator indices. Although we found no consistent association between winter feeding and higher calf:cow ratios, we did not assess late winter mortality and differences in human offtake between fed and unfed regions, which remain a priority for future research. Published 2015. This article is a U.S. Government work and is in the public domain in the USA.

Bottom-up and top-down influences on pregnancy rates and recruitment of northern Yellowstone elk

Declines in calf recruitment in some Rocky Mountain elk populations have raised concerns that recovering carnivore populations may be limiting elk population growth. To help resolve continuing questions about the influence of wolves (Canis lupus) reintroduced during 1995–1997 on elk calf production and survival, we conducted retrospective modeling of factors such as weather, elk density, and recovering carnivore populations potentially affecting northern Yellowstone elk pregnancy and calf survival using a long-term data set collected during 1985–2008. We found elk density negatively affected yearling pregnancy rate but had little effect on adult pregnancy rate. Adult pregnancy rate declined as individuals aged and increased following summers with higher precipitation but did not vary across a wide range of carnivore densities. Fall lactation rates, an indicator of early-season calf survival, increased with elk age and decreased as the ratio of grizzly bear (Ursus arctos horribilis) per elk increased. Over the 23 years of this study, the index of calf recruitment decreased as the wolf/elk ratio increased, decreased following severe winters, and increased as elk density decreased. Estimates of the wolf/elk ratio effect on calf recruitment were negative and confidence intervals did not overlap 0, whereas estimates of the wolf/elk ratio effect on elk pregnancy and early calf survival were positive and confidence intervals did overlap 0. Although a myriad of factors affect each stage leading to calf recruitment, and some of these factors such as weather are out of management control, management actions aimed at reducing wolf densities may result in increasing calf survival and elk population growth rates. However, the desire to manage wolf numbers to achieve a balance with ungulate population objectives must be balanced with other social considerations such as the desire to maintain wolf populations for tourism and wildlife-watching opportunities. © 2014 The Wildlife Society.

Fluke abundance versus host age for an invasive trematode (Dicrocoelium dendriticum) of sympatric elk and beef cattle in southeastern Alberta, Canada.

Epidemiological parameters such as transmission rate, rate of parasite-induced host mortality, and rate of development of host defenses can be assessed indirectly by characterizing the manner in which parasite burdens change with host age. For parasites that are host generalists, estimates of these important parameters may be host-species dependent. In a cross-sectional study, we determined age-abundance profiles of infection in samples of sympatric free-ranging elk and domestic cattle infected with the lancet liver fluke, Dicrocoelium dendriticum. This parasite was introduced into Cypress Hills Provincial Park in southeastern Alberta, Canada in the mid 1990s, and now occurs in 60-90% of co-grazing elk and beef cattle examined at necropsy. The livers of 173 elk were made available by hunters during the 1997-2011 hunting seasons and livers from 35 cattle were purchased from ranchers. In elk, median worm abundance peaked in 6-24 month-olds (median = 72, range = 0-1006) then significantly declined to <10 worms/host in 10-16 year olds. The decline in fluke burden with age is not consistent with an age-related decline in exposure to metacercariae in intermediate hosts and high rates of fluke-induced host mortality are unlikely. Rather, the pattern of peak fluke burdens in elk calves and juveniles, followed by a decline in older animals is consistent with the development of a protective immune response in older hosts. There was no pattern of worm accumulation or decline in sympatric cattle, although statistical power to detect a significant effect was low. These results highlight the complexity and context-dependent nature of epidemiological processes in multi-host systems.

Post-parturition habitat selection by elk calves and adult female elk in New Mexico

Neonatal survival and juvenile recruitment are crucial to maintaining viable elk (Cervus elaphus) populations. Neonate survival is known to be influenced by many factors, including bed-site selection. Although neonates select the actual bed-site location, they must do so within the larger calf-rearing area selected by the mother. As calves age, habitat selection should change to meet the changing needs of the growing calf. Our main objectives were to characterize habitat selection at 2 spatial scales and in areas with different predator assemblages in New Mexico. We evaluated bed-site selection by calves and calf-rearing area selection by adult females. We captured 108 elk calves by hand and fitted them with ear tag transmitters in two areas in New Mexico: the Valle Vidal and Blue Range Wolf Recovery Area. In both study areas, we found that concealing cover structure and distance to that cover influenced bed-site selection of young calves (i.e.,<2 weeks ofage).Oldercalves (i.e., 3-10 weeks ofage) stillselected areas inrelation to distance to cover, but also preferred areas with higher visibility. At the larger spatial scale of calf-rearing habitat selection by the adult female,concealingcover (e.g., rocks,shrubs, and logs) andothervariablesimportant to thehidingcalves were still in the most supported models, but selection was also influenced by forage availability and indices of forage quality. Studies that seek to obtain insight into microhabitat selection of ungulate neonates should consider selection by the neonate and selection by the adult female, changes in selection as neonates age, and potential selection differences in areas of differing predation risk. By considering these influences together andatmultiplescales,studiescanachieve abroaderunderstandingofneonatal ungulate habitatrequirements. Published 2014. This article is a U.S. Government work and is in the public domain in the USA.

Cougar kill rates and prey selection in a multiple-prey system in northeast Oregon

Cougars (Puma concolor) are a primary predator of mule deer (Odocoileus hemionus) and elk (Cervus elaphus) throughout western North America. Effective management of predator-prey systems requires a solid understanding of kill rates, prey use, and selection. We implemented a 3-year study in northeast Oregon to investigate cougar diet, kill rates, and prey selection in a multiple-prey system to assess the degree to which patterns in cougar predation may be generalizable across systems and to identify selective predation patterns of cougars that may affect ungulate populations. We marked 25 adult cougars with global positioning system (GPS) collars and monitored predation sequences for 7,642 days to identify kill sites. In field investigation of kill sites, we identified remains of 1,213 prey items killed by cougars, of which 1,158 (95.4%) were native ungulates. On average, cougars killed 1.03 ungulates/week (95% CI = 0.92–1.14), but kill rates varied by season, sex, and reproductive status of cougars. Cougars killed ungulate prey 1.55 (95% CI = 1.47–1.66) times more frequently during summer (May–Oct) than winter (Nov–Apr). Kill rates were higher in summer because juvenile ungulates were the most frequently killed prey item and were smaller than prey killed in winter. Female cougars with kittens >6 months old killed prey more frequently than males, solitary females, and females with kittens <6 months old likely in response to the increased energetic burden of raising kittens. Male cougars killed larger prey than females, which likely explains why males killed at similar rates as solitary females, despite the larger body size of males. We documented patterns in prey selection influenced by season and demographic classification of cougars. Diets of male cougars included roughly equal amounts of elk (52.2%) and deer (47.8%), whereas diets of females were dominated by deer (74.6%). Male and female cougars displayed strong patterns of selection for elk calves during summer. During winter, female cougars selected deer fawns and males selected elk calves. Female cougars with kittens >6 months old demonstrated little selection for any age class or species of prey, highlighting an opportunistic foraging strategy to maximize energy gains while feeding young. Across all cougars, we observed a pattern of selection for adult male deer during winter but not summer and did not observe patterns of selection for adult elk according to sex. Our results strongly supported the hypothesis proposed by [Knopff et al. (2010) Journal of Wildlife Management, 74: 1435–1447] that cougar predation is influenced by season and demographic classifications of cougars and our results provide strong evidence that this hypothesis should be generalizable to other areas. The patterns of selection for juvenile elk and deer suggested wildlife managers should consider the potential negative effects of cougars on ungulate populations in areas where juvenile recruitment has been chronically low. © 2014 The Wildlife Society.

Range Constraints for Introduced Elk in Southwest Yukon, Canada

Forage availability, snow depths, and winter temperatures were assessed to determine if they might impose range constraints on introduced elk (Cervus elaphus) that voluntarily colonized a 95 km2 area of southwest Yukon (Canada) in 1959. Parkland-like vegetation of stunted aspen (Populus tremuloides) and nonforest upland plant communities, which is atypical vegetation for a boreal forest environment, composed 30% of the colonized area. About 95% of the area produced less than 300 kg/ha of forage, which represents poor productivity compared to more southern elk ranges. In the remaining 5%, indigenous graminoid communities produced (average ± SD) 408 ± 131 kg/ha of forage, exceeded only by nonindigenous roadside vegetation with 652 ± 115 kg/ha. Data from radio-collared animals indicated that most elk occurrences (38% year-round) were associated with parkland-like vegetation, and fecal pellet groups were six times as frequent in indigenous graminoid vegetation as in forest vegetation. Late February 2011 snow depths of 41 ± 7 cm, during a year with a below-normal snowfall, suggested a potential for reduced winter access to forage. Meteorological data from 1981 – 2010 indicate that one-third of winter daily minima in the study area were likely lower than −20˚C, a threshold below which the metabolism of an elk calf must increase to maintain its body temperature. Each assessed habitat variable was unfavorable to elk compared with other western North American winter ranges, which may have limited the development of a more robust population in the southwestern Yukon.

First detection of Schmallenberg virus in elk (Alces alces) indicating infection of wildlife in Białowieża National Park in Poland

Schmallenberg virus (SBV) RNA was detected in the serum of an elk (Alces alces) calf captured on the outskirts of Białowieża National Park (BNP) in December 2012, and shortly afterwards the calf died of acute bronchopneumonia. Serum samples from 169 animals, including bison, red and fallow deer, originating from eight locations situated in four Polish Provinces, were tested for the presence of SBV-specific antibodies between 2011 and 2013. Although no antibodies were found in samples collected up to July 2012, positive samples subsequently appeared between November 2012 and January 2013 in all of the sampled regions. The introduction of SBV infection to the European bison (Bison bonasus) population of BNP between July and November 2012 was also confirmed.

Grizzly bear predation links the loss of native trout to the demography of migratory elk in Yellowstone

The loss of aquatic subsidies such as spawning salmonids is known to threaten a number of terrestrial predators, but the effects on alternative prey species are poorly understood. At the heart of the Greater Yellowstone ecosystem, an invasion of lake trout has driven a dramatic decline of native cutthroat trout that migrate up the shallow tributaries of Yellowstone Lake to spawn each spring. We explore whether this decline has amplified the effect of a generalist consumer, the grizzly bear, on populations of migratory elk that summer inside Yellowstone National Park (YNP). Recent studies of bear diets and elk populations indicate that the decline in cutthroat trout has contributed to increased predation by grizzly bears on the calves of migratory elk. Additionally, a demographic model that incorporates the increase in predation suggests that the magnitude of this diet shift has been sufficient to reduce elk calf recruitment (4-16%) and population growth (2-11%). The disruption of this aquatic-terrestrial linkage could permanently alter native species interactions in YNP. Although many recent ecological changes in YNP have been attributed to the recovery of large carnivores--particularly wolves--our work highlights a growing role of human impacts on the foraging behaviour of grizzly bears.

Animal migration amid shifting patterns of phenology and predation: lessons from a Yellowstone elk herd

Migration is a striking behavioral strategy by which many animals enhance resource acquisition while reducing predation risk. Historically, the demographic benefits of such movements made migration common, but in many taxa the phenomenon is considered globally threatened. Here we describe a long-term decline in the productivity of elk (Cervus elaphus) that migrate through intact wilderness areas to protected summer ranges inside Yellowstone National Park, USA. We attribute this decline to a long-term reduction in the demographic benefits that ungulates typically gain from migration. Among migratory elk, we observed a 21-year, 70% reduction in recruitment and a 4-year, 19% depression in their pregnancy rate largely caused by infrequent reproduction of females that were young or lactating. In contrast, among resident elk, we have recently observed increasing recruitment and a high rate of pregnancy. Landscape-level changes in habitat quality and predation appear to be responsible for the declining productivity of Yellowstone migrants. From 1989 to 2009, migratory elk experienced an increasing rate and shorter duration of green-up coincident with warmer spring-summer temperatures and reduced spring precipitation, also consistent with observations of an unusually severe drought in the region. Migrants are also now exposed to four times as many grizzly bears (Ursus arctos) and wolves (Canis lupus) as resident elk. Both of these restored predators consume migratory elk calves at high rates in the Yellowstone wilderness but are maintained at low densities via lethal management and human disturbance in the year-round habitats of resident elk. Our findings suggest that large-carnivore recovery and drought, operating simultaneously along an elevation gradient, have disproportionately influenced the demography of migratory elk. Many migratory animals travel large geographic distances between their seasonal ranges. Changes in land use and climate that disparately influence such seasonal ranges may alter the ecological basis of migratory behavior, representing an important challenge for, and a powerful lens into, the ecology and conservation of migratory taxa.

Dietary adjustability of grizzly bears and American black bears in Yellowstone National Park

AbstractGrizzly bears (Ursus arctos) and American black bears (U. americanus) are sympatric in much of Yellowstone National Park. Three primary bear foods, cutthroat trout (Oncorhynchus clarki), whitebark pine (Pinus albicaulis) nuts, and elk (Cervus elaphus), have declined in recent years. Because park managers and the public are concerned about the impact created by reductions in these foods, we quantified bear diets to determine how bears living near Yellowstone Lake are adjusting. We estimated diets using: 1) stable isotope and mercury analyses of hair samples collected from captured bears and from hair collection sites established along cutthroat trout spawning streams and 2) visits to recent locations occupied by bears wearing Global Positioning System collars to identify signs of feeding behavior and to collect scats for macroscopic identification of residues. Approximately 45 ± 22% (${\bar {x}}$ ± SD) of the assimilated nitrogen consumed by male grizzly bears, 38 ± 20% by female grizzly bears, and 23 ± 7% by male and female black bears came from animal matter. These assimilated dietary proportions for female grizzly bears were the same as 10 years earlier in the Lake area and 30 years earlier in the Greater Yellowstone Ecosystem. However, the proportion of meat in the assimilated diet of male grizzly bears decreased over both time frames. The estimated biomass of cutthroat trout consumed by grizzly bears and black bears declined 70% and 95%, respectively, in the decade between 1997–2000 and 2007–2009. Grizzly bears killed an elk calf every 4.3 ± 2.7 days and black bears every 8.0 ± 4.0 days during June. Elk accounted for 84% of all ungulates consumed by both bear species. Whitebark pine nuts continue to be a primary food source for both grizzly bears and black bears when abundant, but are replaced by false‐truffles (Rhizopogon spp.) in the diets of female grizzly bears and black bears when nut crops are minimal. Thus, both grizzly bears and black bears continue to adjust to changing resources, with larger grizzly bears continuing to occupy a more carnivorous niche than the smaller, more herbivorous black bear. © 2012 The Wildlife Society.

Passive transfer of maternal GnRH antibodies does not affect reproductive development in elk (Cervus elaphus nelsoni) calves

Gonadotropin-releasing hormone is intermittently released from the hypothalamus in consistent patterns from before birth to final maturation of the hypothalamic-pituitary-gonadal axis at puberty. Disruption of this signaling via GnRH vaccination during the neonatal period can alter reproduction at maturity. The objective of this study was to investigate the long-term effects of GnRH-antibody exposure on reproductive maturation and function in elk calves passively exposed to high concentrations of GnRH antibodies immediately after birth. Fifteen elk calves (eight males and seven females) born to females treated with GnRH vaccine or sham vaccine during midgestation were divided into two groups based on the concentration of serum GnRH antibodies measured during the neonatal period. Those with robust (>15 pmol 125I-GnRH bound per mL of serum) titers (N = 10; four females and six males) were designated as the exposed group, whereas those with undetectable titers (N = 5; three females and two males) were the unexposed group. Onset of puberty, reproductive development, and endocrine function in antibody-exposed and unexposed male and female elk calves were compared. Neonatal exposure to high concentrations of GnRH antibodies had no effect on body weight (P = 0.968), endocrine profiles (P > 0.05), or gametogenesis in either sex. Likewise, there were no differences between groups in gross or histologic structure of the hypothalamus, pituitary, testes, or ovaries. Pituitary stimulation with a GnRH analog before the second potential reproductive season induced substantial LH secretion in all experimental elk. All females became pregnant during their second reproductive season and all males exhibited similar mature secondary sexual characteristics. There were no differences between exposure groups in hypothalamic GnRH content (P = 0.979), pituitary gonadotropin content (P > 0.05) or gonadal structure. We concluded that suppressing GnRH signaling through immunoneutralization during the neonatal period likely does not alter long-term reproductive function in this species.

Demographic balancing of migrant and resident elk in a partially migratory population through forage–predation tradeoffs

Partial migration is widespread in ungulates, yet few studies have assessed demographic mechanisms for how these alternative strategies are maintained in populations. Over the past two decades the number of resident individuals of the Ya Ha Tinda elk herd near Banff National Park has been increasing proportionally despite an overall population decline. We compared demographic rates of migrant and resident elk to test for demographic mechanisms partial migration. We determined adult female survival for 132 elk, pregnancy rates for 150 female elk, and elk calf survival for 79 calves. Population vital rates were combined in Leslie‐matrix models to estimate demographic fitness, which we defined as the migration strategy‐specific population growth rate. We also tested for differences in factors influencing risk of mortality between migratory strategies for adult females using Cox‐proportional hazards regression and time‐varying covariates of exposure to forage biomass, wolf predation risk, and group size. Despite higher pregnancy rates and winter calf weights associated with higher forage quality, survival of migrant adult females and calves were lower than resident elk. Resident elk traded high quality food to reduce predation risk by selecting areas close to human activity, and by living in group sizes 20% larger than migrants. Thus, residents experienced higher adult female survival and calf survival, but lower pregnancy and calf weights. Cause‐specific mortality of migrants was dominated by wolf and grizzly bear mortality, whereas resident mortality was dominated by human hunting. Demographic differences translated into slightly higher (2–3%), but non‐significant, resident population growth rate compared to migrant elk, suggesting demographic balancing between resident strategies during our study. Despite statistical equivalence, our results are also consistent with slow long‐term declines in migrants because of high predation because of higher wolf‐caused mortality in migrants. These results emphasize that migrants and residents will make different tradeoffs between forage and risk may affect the demographic balance of partially migratory populations, which may explain recent declines in migratory behavior in many ungulate populations around the world.

Cougar survival and source‐sink structure on Greater Yellowstone's Northern Range

AbstractWe studied survival and causes of mortality of radiocollared cougars (Puma concolor) on the Greater Yellowstone Northern Range (GYNR) prior to (1987–1994) and after wolf (Canis lupus) reintroduction (1998–2005) and evaluated temporal, spatial, and environmental factors that explain variation in adult, subadult, and kitten survival. Using Program MARK and multimodel inference, we modeled cougar survival based on demographic status, season, and landscape attributes. Our best models for adult and independent subadults indicated that females survived better than males and survival increased with age until cougars reached older ages. Lower elevations and increasing density of roads, particularly in areas open to cougar hunting north of Yellowstone National Park (YNP), increased mortality risks for cougars on the GYNR. Indices of ungulate biomass, cougar and wolf population size, winter severity, rainfall, and individual characteristics such as the presence of dependent young, age class, and use of Park or Wilderness were not important predictors of survival. Kitten survival increased with age, was lower during winter, increased with increasing minimum estimates of elk calf biomass, and increased with increasing density of adult male cougars. Using our best model, we mapped adult cougar survival on the GYNR landscape. Results of receiver operating characteristic (ROC) analysis indicated a good model fit for both female (area under the curve [AUC] = 0.81, 95%CI = 0.70–0.92, n = 35 locations) and male cougars (AUC = 0.84, 95%CI = 0.74–0.94, n = 49 locations) relative to hunter harvest locations in our study area. Using minimum estimates of survival necessary to sustain the study population, we developed a source‐sink surface and we identify several measures that resource management agencies can take to enhance cougar population management based on a source‐sink strategy. © 2011 The Wildlife Society.

Survival and cause‐specific mortality of elk Cervus canadensis calves in a predator rich environment

AbstractQuantification of basic demographic parameters such as survival rates and cause‐specific mortality is important for effective species management. We conducted a 4‐year study (during May 2005‐June 2009) of elk Cervus canadensis calf survival and cause‐specific mortality in Pennsylvania, USA. We captured and radio‐collared 93 elk calves ≤ 7 days old and monitored them weekly to detect mortality and cause of death. Of the 93 radio‐collared elk calves, 15 (16%) died during our study. Despite high black bear Ursus americanus and coyote Canis latrans densities, none of the mortalities were the result of predation. Causes of death included poaching (N = 3), legal harvest (N = 2), road kill (N = 2), pneumonia (N = 1) and rumen acidosis (N = 1). We were unable to determine the cause of mortality for six of the elk calves; however, predation was eliminated as a possible source of mortality in all unknown cases. Survival probabilities were similar between sexes and among years. Summer survival (birth‐31 October) was 0.92 (SE = 0.03, N = 93) and winter survival (1 November ‐ 1 April) was 0.90 (SE = 0.04, N = 79). Annual estimated elk calf survival was 0.82 (SE = 0.04, N = 93). Our findings suggest that Pennsylvania elk calves have a &gt; 80% chance of survival to one‐year of age, despite high densities of predators known to influence elk calf survival elsewhere. The high calf survival rates that we observed indicate the availability of high quality habitat leading to excellent physical condition of elk.

Neonatal mortality of elk driven by climate, predator phenology and predator community composition

1. Understanding the interaction among predators and between predation and climate is critical to understanding the mechanisms for compensatory mortality. We used data from 1999 radio-marked neonatal elk (Cervus elaphus) calves from 12 populations in the north-western United States to test for effects of predation on neonatal survival, and whether predation interacted with climate to render mortality compensatory. 2. Weibull survival models with a random effect for each population were fit as a function of the number of predator species in a community (3-5), seven indices of climatic variability, sex, birth date, birth weight, and all interactions between climate and predators. Cumulative incidence functions (CIF) were used to test whether the effects of individual species of predators were additive or compensatory. 3. Neonatal elk survival to 3 months declined following hotter previous summers and increased with higher May precipitation, especially in areas with wolves and/or grizzly bears. Mortality hazards were significantly lower in systems with only coyotes (Canis latrans), cougars (Puma concolor) and black bears (Ursus americanus) compared to higher mortality hazards experienced with gray wolves (Canis lupus) and grizzly bears (Ursus horribilis). 4. In systems with wolves and grizzly bears, mortality by cougars decreased, and predation by bears was the dominant cause of neonatal mortality. Only bear predation appeared additive and occurred earlier than other predators, which may render later mortality by other predators compensatory as calves age. Wolf predation was low and most likely a compensatory source of mortality for neonatal elk calves. 5. Functional redundancy and interspecific competition among predators may combine with the effects of climate on vulnerability to predation to drive compensatory mortality of neonatal elk calves. The exception was the evidence for additive bear predation. These results suggest that effects of predation by recovering wolves on neonatal elk survival, a contentious issue for management of elk populations, may be less important than the composition of the predator community. Future studies would benefit by synthesizing overwinter calf and adult-survival data sets, ideally from experimental studies, to test the roles of predation in annual compensatory and additive mortality of elk.

Differential prey use by male and female cougars in Washington

AbstractMale and female predators are often assumed to have the same effects on prey. Because of differences in body size and behavior, however, male and female predators may use different species, sexes, and ages of prey, which could have important implications for wildlife conservation and management. We tested for differential prey use by male and female cougars (Puma concolor) from 2003 to 2008 in Washington State. We predicted that male cougars would kill a greater proportion of larger and older prey (i.e., adult elk [Cervus elaphus]), whereas females would kill smaller and younger prey (i.e., elk calves, mule deer [Odocoileus hemionus]). We marked cougars with Global Positioning System (GPS) radio collars and investigated 436 predation sites. We located prey remains at 345 sites from 9 male and 9 female cougars. We detected 184 mule deer, 142 elk, and 17 remains from 4 other species. We used log‐linear modeling to detect differences in species and age of prey killed among cougar reproductive classes. Solitary females and females with dependent offspring killed more mule deer than elk (143 vs. 83, P &lt; 0.01), whereas males killed more elk than mule deer (59 vs. 41, P &lt; 0.01). Proportionately, males killed 4 times more adult elk than did females (24% vs. 6% of kills) and females killed 2 times more adult mule deer than did males (26% vs. 15% of kills). Managers should consider the effects of sex of predator in conservation and management of ungulates, particularly when managing for sensitive species. © 2011 The Wildlife Society.

Effects of black bear relocation on elk calf recruitment at Great Smoky Mountains National Park

AbstractPrevious research from 2001 to 2006 on an experimentally released elk (Cervus elaphus) population at Great Smoky Mountains National Park (GSMNP or Park) indicated that calf recruitment (i.e., calves reaching 1 yr of age per adult female elk) was low (0.306, total SE = 0.090) resulting in low or negative population growth (λ = 0.996, 95% CI = 0.945–1.047). Black bear (Ursus americanus) predation was the primary calf mortality factor. From 2006 to 2008, we trapped and relocated 49 bears (30 of which were radiocollared) from the primary calving areas in the Park and radiomonitored 67 (28 M:39 F) adult elk and 42 calves to compare vital rates and population growth with the earlier study. A model with annual calf recruitment rate correlating with the number of bears relocated each year was supported (ΔAICc = 0.000; β = 0.070, 95% CI = 0.028–0.112) and a model with annual calf recruitment differing from before to during bear relocation revealed an increase to 0.544 (total SE = 0.098; β = −1.092, 95% CI = −1.180 to −0.375). Using vital rates and estimates of process standard errors observed during our study, 25‐yr simulations maintained a mean positive growth rate in 100% of the stochastic trials with λ averaging 1.118 (95% CI = 1.096–1.140), an increase compared with rates before bear relocation. A life table response experiment revealed that increases in population growth were mostly (67.1%) due to changes in calf recruitment. We speculate that behavioral adaptation of the elk since release also contributed to the observed increases in recruitment and population growth. Our results suggest that managers interested in elk reintroduction within bear range should consider bear relocation as a temporary means of increasing calf recruitment. © 2011 The Wildlife Society.

Maternal Passive Transfer of GnRH Antibodies Does Not Change Reproductive Development in Elk Calves.

Maternal Passive Transfer of GnRH Antibodies Does Not Change Reproductive Development in Elk Calves.

Influence of Predator Harvest, Biological Factors, and Landscape on Elk Calf Survival in Idaho

ABSTRACT We evaluated survival of elk (Cervus elaphus) calves on 2 contrasting study areas in north‐central Idaho, USA, from 1997 to 2004. Recruitment was modest (&gt;30 calves:100 F [calves of either sex: F elk 1 yr old]) and stable on the South Fork study area and low (&lt;20 calves:100 F) and declining on the Lochsa study area. The primary proximate cause of calf mortality on both study areas was predation by black bears (Ursus americanus) and mountain lions (Puma concolor). We experimentally manipulated populations of black bears and mountain lions on a portion of each study area. Black bear harvest (harvest density/600km2) initially doubled on the Lochsa treatment after manipulating season bag limits. Mountain lion harvest also increased by 60% but varied widely during the manipulation period. Harvest seasons were closed for black bears and mountain lions on the treatment portion of the South Fork study area. Using the Andersen—Gill formulation (A‐G) of the Cox proportional hazards model, we examined effects of landscape structure, predator harvest levels, and biological factors on summer calf survival. We used Akaike's Information Criterion (AICc) and multimodel inference to assess some potentially useful predictive factors relative to calf survival. We generated risk ratios for both the best models and for model‐averaged coefficients. Our models predicted that calf survival was influenced by biological factors, landscape surrounding calf locations, and predator harvest levels. The model that best explained mortality risk to calves on the Lochsa included black bear harvest (harvest density/600 km2), estimated birth mass of calves, and percentage of shrub cover surrounding calf locations. Incorporating a shrub X time interaction allowed us to correct for nonproportionality and detect that effect of shrub cover was only influential during the first 14 days of a calf's life. Model‐averaging indicated that estimated birth mass of calves and black bear harvest were twice as important as the next variables, but age of calves at capture was also influential in calf survival. The model that best explained mortality risk to calves on the South Fork included black bear harvest, age of calves at capture, and gender of calves. Model‐averaging indicated that age at capture and black bear harvest were twice as important as the next variable, forest with 33–66% canopy cover (Canopy 33–66). Risk to calves decreased when calves occupied areas with more of this forest cover type. Model‐averaging also indicated that increased mountain lion harvest lowered calf mortality risk 4% for every 1‐unit increase in lion harvest (harvest density/600 km2) but was lower (&lt;25%) in importance compared to age at capture and black bear harvest. Our results suggest that levels of predator harvest, and presumably predator density, resource limitations expressed through calf birth mass, and habitat structure had substantial effects on calf survival. Our results can be generalized to other areas where managers are dealing with low calf elk recruitment. However, because factors vary spatially, a single management strategy applied in different areas will probably not have the same effect on calf survival.

Wolf, &lt;em&gt;Canis lupus&lt;/em&gt;, Avoidance Behaviour of American Elk, &lt;em&gt;Cervus elaphus&lt;/em&gt;, in Jasper National Park, Alberta

An American Elk calf (Cervus elaphus) that was captured near human habitation in Jasper National Park, Alberta, was fitted with a radio-collar and released 40 km away in the park's main valley of the Athabasca River. The calf joined a local herd of elk, and its radio signal revealed that the elk, in two months' time, travelled eight times back and forth between the herd's traditional semi-open winter range at Devona and a largely wooded area at Rocky River &gt;3 km away. Each time, on their trans-valley route the elk crossed a busy highway, a railway, and a partly frozen river. Sightings of elk and Wolves (Canis lupus) were inversely correlated on 97 days of observation at Devona. We conclude that the elk's migrations were prompted by their urge to avoid and flee from Wolves, which were common at both locations.