Suchergebnisse

Content
Native communities of herbivores have evolved fundamental dietary niches that avoid or minimise competition; the introduction of exotic species can change dietary niches, cause overlap in resource use, and result in competition for resources.

Aims
We compared niche breadth, overlap in diet, and quality of diet between introduced sika deer and native white-tailed deer in Maryland, USA. We investigated these changes in free-ranging populations where both species are allopatric as well as when they are sympatric.

Methods
We used microhistological analysis of faecal samples to determine the percentage of resources used by sika deer and white-tailed deer, as measured between geographical areas of similar habitat quality. We compared resource use specifically by controlling for harvest pressure and resource availability, which are known to alter resource use other than the presence of an additional deer species.

Key results
We observed a significant resource overlap (range 63–88%) between species. In the presence of sika deer, white-tailed deer displayed an increased niche breadth (108%) and a lower diet quality (17%). Sika deer consumed the same resources that comprised 78% of white-tailed deer diet. Unlike other native ungulates that have dietary overlap with white-tailed deer, sika deer is neither temporally nor geographically segregated in habitat use.

Conclusions
Resource overlap and changes in niche breadth and diet quality during sympatry strongly denote dietary competition between sika deer and white-tailed deer. This competition results in white-tailed deer altering the dietary selection, thereby consuming lower-quality forage.

Implications
White-tailed deer are concentrate selectors and require higher diet quality than do sika deer, which can tolerate diets higher in fibre, consistent with their classification as intermediate feeders. A decrease in the nutritional quality of resources used by white-tailed deer could contribute to the decline of white-tailed deer over time and allow the continued spread of sika deer.

Context
Long-term studies of large, vertebrate mammals using capture–recapture data are scarce, even though long-term ecological studies are requisite to understanding quantitative genetics and evolutionary processes that can be applied as part of management programs.

Aims
Objectives were to (1) partition components of variation in body mass to understand the differential effects of environmental variation on the sexes during ontogeny, to better prescribe habitat-improvement projects, and (2) estimate repeatability to assess potential for selection on body mass.

Methods
We used a 23-year dataset (1983–2005) of capture–recapture records of wild white-tailed deer (Odocoileus virginianus) to estimate components of variance and repeatability of body mass. We used an animal-model approach that employed the use of general linear mixed models and restricted maximum likelihood to adjust for the effects of age (i.e. fixed effect), and to partition the total phenotypic variance into among-individual (i.e. the deer), permanent environmental (i.e. year of birth) and temporary environmental (i.e. year of measurement and residual) effects (all modelled as random effects).

Key results
We found that body mass increased with age in both sexes, repeatability of body mass was 0.595 for females and 0.716 for males, and among-individual variation was more influential on body mass than were permanent and temporary environmental effects combined. Year of birth was more important in males than females, but changed during the course of ontogeny for both sexes. Year of measurement did not influence post-rut body mass in males, but did contribute to variation in body mass of females.

Conclusions
These long-term data offer insights into the sources of variation that influence body mass of deer, which can be used to understand how environmental sources of variation influence phenotypic traits, and for developing management plans and making selection decisions.

Implications
Knowledge of repeatability (as an upper limit to heritability) can be used to make management decisions related to selection, culling and breeding, whereas understanding environmental effects can lead to better management recommendations (e.g. habitat-improvement projects).

Context Feral pigs represent a significant threat to agriculture and ecosystems and are disease reservoirs for pathogens affecting humans, livestock and other wildlife. Information on the behavioural ecology of feral pigs might increase the efficiency and effectiveness of management strategies. Aims We assessed the frequency of promiscuous mating in relation to oestrous synchrony in feral pigs from southern Texas, USA, an agroecosystem with a widespread and well established population of feral pigs. An association between multiple paternity of single litters and synchrony of oestrous may indicate alternative mating strategies, such as mate-guarding. Methods We collected gravid sows at nine sites in southern Texas during 2005–07. We used a panel of DNA microsatellite markers to estimate frequency of multiple paternity and the distribution of male mating among litters of feral pigs. Conception dates were determined by fitting average fetal crown–rump measurements within litters to expected fetal development relative to gestation time. Key results We found evidence of multiple paternity in 21 of 64 litters (33%) from seven of nine sites sampled. Synchrony of oestrous did not influence promiscuous mating, as we found multiple paternity at sites with synchronous and asynchronous oestrous. Males sired from 8 to 11 offspring at three sites where >10 litters were sampled. Mean litter size (5.4) was less than the best-fit value for the number of offspring, indicating that some males sired offspring with ≥ 2 females. Key conclusions Feral pigs in Texas appear to be promiscuous under a range of demographic conditions, unlike wild boar and feral pigs in other regions. The ecological and behavioural factors affecting multiple paternity are not clear, but may include male–male competition, harassment avoidance, genetic benefits for offspring, response to macro-habitat conditions, or selection. Implications A high incidence of sexual contact among individuals may increase the opportunity for diseases transmitted by oral or venereal routes, such as swine brucellosis and pseudorabies. In addition, fertility-control methods targeting males only are likely to be inefficient if female promiscuity is high; methods targeting females or both sexes jointly may be more effective.

Abstract Context The ability to accurately estimate age of animals is important for both research and management. The two methods for age estimation in ungulates are tooth replacement and wear (TRW) and cementum annuli (CA). Errors in estimated TRW ages are commonly attributed to environmental conditions; however, the influence of environmental variables on tooth wear has not been quantified. Further, the performance of CA in environments with weak seasonality has not been thoroughly evaluated. Aims The study had the following three goals: identify environmental and morphological factors that influenced estimated ages, quantify accuracy of TRW and CA, and develop TRW ageing criteria that minimise error. Methods We used data from harvested (n = 5117) and free-ranging, known-age white-tailed deer (n = 134) collected in southern Texas, USA, to quantify environmental and morphological influences on estimated TRW ages, and assess biases in both methods. Key results We observed substantial variation in age estimates for both TRW and CA. Soil, drought and supplemental nutrition had minor effects on tooth wear, insufficient to alter age estimates by ≥1 year. Body mass and antler size influenced age estimates for TRW only for extreme outliers. Both methods were biased and tended to under-estimate ages of adult deer, especially TRW. Wear on the first molar was most correlated with the known age (r2 = 0.78) and allowed biologists to correctly place known-age deer into age classes of 2, 3–5, and ≥6 years old 72%, 73% and 68% of the time, an improvement compared with the 79%, 48% and 28% accuracy from pooled TRW. Conclusions We observed substantial inter- and intra-individual variation in tooth-wear patterns that became more pronounced in older deer. Individual variation had a greater influence on TRW ages than did environmental covariates, whereas CA ages appeared unaffected by environment. Although variable, age estimates were ±1 year of the true age 87% and 93% of the time for TRW and CA respectively. Implications Managers, ecologists and epidemiologists often incorporate ages into population models. The high inter-individual variation in estimated ages, the tendency to underestimate ages of older deer, and the ageing method need to be considered.

Context The expansion of feral pig populations across the United States has increased the occurrence of damage and damage complaints. New techniques are needed to more effectively manage feral pig damage, including the development of fertility control agents. Aims We aimed to assess the ovotoxic properties of ERL-4221 as a candidate fertility control agent for feral pigs. Methods We conducted two palatability trials to determine ERL-4221 acceptance and one experimental trial with ERL-4221 at the captive wildlife facility of Texas A&M University-Kingsville during 2008. Our experimental trial had three treatments, a control containing no ERL-4221, baits containing 16.0 mg ERL-4221 kg–1 bodyweight for 10 days, and baits containing 16.0 mg ERL-4221 kg–1 bodyweight for 20 days. Key results Final body mass, total ovary mass, number of follicles and number of corpora lutea did not differ between treatments. Conclusions We did not find it efficacious to orally deliver ERL-4221 to feral pigs to reduce fertility. Oral delivery is the most practical, cost-effective means of delivering fertility control agents to feral pigs and development of additional fertility control strategies are needed. Implications Unless ovotoxic effects of ERL-4221 can be identified in feral pigs, along with a successful means of administration, other fertility control strategies may need to be explored, such as oocyte-secreted proteins that regulate follicular development.

Context Research on large, terrestrial mammals often requires physical captures to attach tags or collars, collect morphological data, and collect biological samples. Choice of capture method should minimise pain and distress to the animal, minimise risk to personnel, and consider whether the method can achieve study objectives without biasing results. Aims We studied how capture via helicopter net-gunning affected survival, post-capture movement patterns, and space use of exotic nilgai (Boselaphus tragocamelus) in southern Texas, USA. Methods We estimated daily survival rates for 101 collared nilgai over 28 days, following 125 captures. We calculated mean daily movement rates and net-squared displacement for 21 recaptured nilgai for 60 days, starting 30 days before capture. Key results The survival probability of 125 nilgai individuals was 0.97 (95% CI = 0.92–0.99) over the 28 days following capture, with the lowest daily survival for the day after capture ( x ¯ WR22049_IE1.gif = 0.99; 95% CI = 0.96–1.00). We observed an increase of ~65% in the mean daily movement rate of 134 m/h on the first 2 days since capture, followed by a period of reduced movement out to the 5th day before returning to pre-capture levels. Analysis of net-squared displacement for 21 nilgai showed that 17 resumed pre-capture space-use patterns within a week, whereas four individuals did not return to the pre-capture range for ≥1 month. Conclusions Capture-related mortality rates for nilgai using helicopter net-gunning in our study (3%) were similar or lower than those reported for similar species captured using the same method. While we were able to detect a period of elevated movement rates, followed by a recovery period of diminished movement as a result of capture, nilgai appeared to return to typical behaviour ~6 days post-capture. Most nilgai in our study also resumed typical space-use patterns within a week of capture; however, our results suggest high individual variability in their response. Implications We recommend using net-gunning from a helicopter as a method for capturing nilgai when conditions and where vegetation and topography allow. We suggest censoring data for a minimum of 7 days following capture for analyses related to survival and movement rates. For analyses relating to space use, we suggest inspecting net-squared displacement or some similar displacement analysis for each animal separately to account for individual variation in response and exclude data accordingly.