The costs and benefits of alternative migratory strategies are often framed in the context of top-down and bottom-up effects on individual fitness. This occurs because migration is considered a costly behavioral strategy that presumably confers explicit benefits to migrants in the form of either decreased predation risk (predation risk avoidance hypothesis) or increased nutrition (forage maturation hypothesis). To test these hypotheses, we studied a partially migratory moose (Alces alces) population and contrasted explicit measures of predation risk (i.e., offspring survival) and nutrition (i.e., accumulation of endogenous energy reserves) between resident and migratory subpopulations. We relied on data collected from migratory and nonmigratory radio-marked moose (n = 67) that inhabited a novel study system located in coastal Alaska between 2004 and 2010. In this area, 30% of the population resides year-round on a coastal foreland area, while 48% migrate to either a small island archipelago or a subalpine ridge system (the remainder exhibited one of six different low-occurrence strategies). Overall, we determined that accumulation of body fat during the growing season did not differ between migratory or resident modalities. However, calf survival was 2.6-2.9 times higher for individuals that migrated (survival, islands = 0.49 +/- 0.16 [mean +/- SE], n = 35; ridge = 0.52 +/- 0.16, n = 33) than those that did not (survival, resident = 0.19 +/- 0.08, n = 57). Our results support the predation risk avoidance hypotheses, and suggest that migration is a behavioral strategy that principally operates to reduce the risk of calf predation and does not confer explicit nutritional benefits. We did not directly detect trade-offs between predation risk and nutrition for migratory individuals. Yet we identify an indirect life history mechanism that may mildly dampen the apparent fitness benefits of migration. The proximate factors accounting for differences in migration-specific neonate survival are likely linked to accessibility of refugial habitats for moose at local and landscape scales, landscape factors that affect hunting efficacy of large carnivores, and interactions with rural human communities. Conservation of ungulate populations can be aided by integrating knowledge about migratory behavior, life history strategies, and factors that alter ungulate vulnerability, particularly those induced by human activity.

Variation in core body temperature of mammals is a result of endogenous regulation of heat from metabolism and the environment, which is affected by body size and life history. We studied moose (Alces alces) in Alaska to examine the effects of endogenous and exogenous factors on core body temperature at seasonal and daily time scales. We used a modified vaginal implant transmitter to record core body temperature in adult female moose at 5-min intervals for up to 1 year. Core body temperature in moose showed a seasonal fluctuation, with a greater daily mean core body temperature during the summer (38.2°C, 95% CI = 38.1–38.3°C) than during the winter (37.7°C, 95% CI = 37.6–37.8°C). Daily change in core body temperature was greater in summer (0.92°C, 95% CI = 0.87–0.97°C) than in winter (0.58°C, 95% CI = 0.53–0.63°C). During winter, core body temperature was lower and more variable as body fat decreased among female moose. Ambient temperature and vapor pressure accounted for a large amount of the residual variation (0.06–0.09°C) in core body temperature after accounting for variation attributed to season and individual. Ambient temperature and solar radiation had the greatest effect on the residual variation (0.17–0.20°C) of daily change in core body temperature. Our study suggests that body temperature of adult female moose is influenced by body reserves within seasons and by environmental conditions within days. When studying northern cervids, the influence of season and body condition on daily patterns of body temperature should be considered when evaluating thermal stress.

Moose rumen samples from Vermont, Alaska and Norway were investigated for methanogenic archaeal and protozoal density using real-time PCR, and diversity using high-throughput sequencing of the 16S and 18S rRNA genes. Vermont moose showed the highest protozoal and methanogen densities. Alaskan samples had the highest percentages of Methanobrevibacter smithii, followed by the Norwegian samples. One Norwegian sample contained 43 % Methanobrevibacter thaueri, whilst all other samples contained < 10 %. Vermont samples had large percentages of Methanobrevibacter ruminantium, as did two Norwegian samples. Methanosphaera stadtmanae represented one-third of sequences in three samples. Samples were heterogeneous based on gender, geographical location and weight class using analysis of molecular variance (AMOVA). Two Alaskan moose contained >70 % Polyplastron multivesiculatum and one contained >75 % Entodinium spp. Protozoa from Norwegian moose belonged predominantly (>50 %) to the genus Entodinium, especially Entodinium caudatum. Norwegian moose contained a large proportion of sequences (25–97 %) which could not be classified beyond family. Protozoa from Vermont samples were predominantly Eudiplodinium rostratum (>75 %), with up to 7 % Diploplastron affine. Four of the eight Vermont samples also contained 5–12 % Entodinium spp. Samples were heterogeneous based on AMOVA, principal coordinate analysis and UniFrac. This study gives the first insight into the methanogenic archaeal diversity in the moose rumen. The high percentage of rumen archaeal species associated with high starch diets found in Alaskan moose corresponds well to previous data suggesting that they feed on plants high in starch. Similarly, the higher percentage of species related to forage diets in Vermont moose also relates well to their higher intake of fibre.

Management and research of moose (Alces alces) in Alaska, USA, often require chemical immobilization; however, moose may be prone to capture‐induced hyperthermia while immobilized. We chemically immobilized moose with carfentanil citrate and xylazine hydrochloride to measure rump fat depth, collect blood and fecal samples, and to deploy modified vaginal implant transmitters and global positioning system (GPS)‐collars for recording body temperature and movement during and after the chemical immobilization. We predicted wild moose pursued and captured from a helicopter would have elevated body temperature at time of capture, whereas body temperature would remain stable in hand‐raised captive moose not pursued and only hand‐injected for immobilization. Additionally, we expected post‐capture body temperature would be a function of activity, time immobilized, and ambient temperature. As predicted, body temperature of wild moose was elevated 1 hour after capture (38.9°C, 95% CI = 38.7–39.1°C) but returned to baseline levels within 3 hours (38.0°C, 95% CI = 37.9–38.1°C); however, body temperatures then rose above baseline levels and remained elevated 12–48 hours post‐capture when movement rates were also elevated. Body temperatures in captive moose were not elevated 1‐hour post‐immobilization (37.9°C, 95% CI = 37.8–38.0°C). Body temperatures of wild moose were positively related to cortisol levels at time of capture. Two moose that died after immobilization had initial body temperatures similar to other immobilized moose; however, their body temperature began to rise at 17 hours and 40 hours post‐immobilization. Our study provides evidence that chemical immobilization affects body temperature and movement of wild moose up to 48 hours after capture, possibly as a result of renarcotization from carfentanil citrate. With advancements in technology, we recommend fine‐scale GPS data (<1‐hr fix rates) and continuous body temperature be evaluated to detect evidence of renarcotization during and after opioid‐based captures of northern ungulates. © 2020 The Wildlife Society.

Measuring body temperature in free-ranging ungulates is challenging. We evaluated a vaginal implant transmitter (TVIT) modified to collect continuous body temperature of captive and wild female moose (Alces alces) in Alaska, USA. We deployed TVITs in 18 moose between 2014 and 2016. We manually removed the TVIT after 51-338 days of deployment and sampled vaginal bacterial flora to assess negative effects of TVIT retention. For comparison, we also sampled vaginal flora from moose that did not have a TVIT. Mean bacterial growth scores were greater for moose with a TVIT than representative vaginal swabs from moose without a TVIT. The TVIT adequately collected body temperature measurements; however, the TVIT design could be improved to fit young, nulliparous moose. TVITs can be easily deployed and removed, but are limited by battery life, can only be deployed in adult female moose, and may increase vaginal bacterial concentrations. Ó