Behavioural factors affecting male reproductive success in red deer (Cervus elaphus)

Variation in reproductive success among adult red deer stags was related to harem size, and the duration and timing of breeding access. All three factors were affected by dominance (fighting success) during the rut. The number of hinds using a stag's rutting area and the duration of individual rutting activity also affected breeding access. Dominance rank in bachelor herds, which may affect access to hinds conceiving after the rut, was correlated with rank in the preceding but not the following rut.     

Seasonal migration of male red deer (<Emphasis Type="Italic">Cervus elaphus</Emphasis>) in southern Sweden and consequences for management

Red deer Cervus elaphus is a highly appreciated and intensively managed game species throughout Europe. A common management objective is a sustainable harvest of large trophies. In southern Sweden, management has mainly aimed at preserving the nominate subspecies C. elaphus elaphus. Seasonal migration of red deer males may, however, complicate both harvest management as well as conservation efforts. I used individually identified male red deer in southern Sweden to observe distance travelled from rutting areas to areas used by males in summer and winter. Adult males were identified by antler shape and photo-documented during rut. Photos from the rut were compared to trophies of deer harvested or found dead, to found cast antlers and to stags photographed during summer. From 1969 to 2007, a distance between rutting ground and summer/winter quarters was established for 96 identified stags. An average distance of 14 km and a maximum distance of 47 km were recorded between rut and summer/winter observations. The seasonal migration of males increases the risk of overexploitation of males with harvest in both rutting areas and wintering areas. Harvest management and conservation efforts may fail if males seasonally migrate outside the management unit. The results suggest that seasonal migration must be considered in harvest management and conservation and that there is a need for a regulation of male harvest. Furthermore, the study stresses that the success in deer management of single hunting units, may be largely dependent on the harvest policies in the near surroundings as well as in areas tenths of kilometres away, suggesting that a successful management must rely on co-operation and co-ordination on a landscape scale.     

Age- and density-dependent reproductive effort in male red deer

Reproductive effort in female ungulates originates from gestation and lactation and has been studied extensively; however, no comparable studies of reproductive effort in males (due to fighting for access to mates) have, to our knowledge, previously been reported. Here, we report on weight loss of male red deer during the annual mating season--a direct measure of male reproductive effort (or somatic reproductive costs). The 'terminal investment' hypothesis predicts that reproductive effort should increase with age, given that costs remain stable. We also propose the 'mating strategy-effort' hypothesis, which predicts that reproductive effort peaks in prime-aged males, since they are most often the harem holders. Consistent with the mating strategy-effort hypothesis, relative weight loss during the rutting season peaked at prime age and was lower in younger and senescent males. Weight loss during the rut was relatively smaller as density increased and more so for older males. This is probably primarily due to males (particularly senescent males) starting their rut in poorer condition at high density. The pattern of reproductive effort in males with regard to age and density therefore differs markedly from the pattern reported for females.     

Seasonal and daily walking activity patterns of free-ranging adult red deer (<Emphasis Type="Italic">Cervus elaphus</Emphasis>) at the individual level

We studied the walking activity over the year of free-ranging adult red deer (Cervus elaphus) in a mountainous area with the aim of describing the dynamics of movement patterns at the individual level. We monitored the distance walked by two males and two females fitted with global positioning system collars to test the hypothesis that deer adopt behaviours to reduce costs of locomotion. We predicted that both sexes would travel less in winter when disadvantageous environmental conditions occurred. We also predicted that the males would (1) reduce their movement soon after the rut due to very high energy expenditure during the breeding season and (2) travel less than the females due to their larger body mass. As we expected, minimum walking activity occurred after the rut from November to February for the males and in late February for the females. The walking activity of males peaked during the rut whereas that of females decreased. But compared to males, females moved more both during winter and daylight hours. Although our study stems from just four individuals, these results and the methodology used can be inspirational for red deer research as well as for ungulate research in general.     

To Feed or Not to Feed? Testing Different Hypotheses on Rut‐Induced Hypophagia in a Mountain Ungulate

In many ruminant species, males dramatically reduce forage intake during the rut. To date, different hypotheses have been suggested to explain this rut‐induced hypophagia. To assess the predictions of the main hypotheses, we analysed Alpine ibex (Capra ibex) activity budget and compared the behaviour of males and females before, during, and after the rut. Only males spent significantly less time foraging during the rut than outside of it, whereas females allocated a similar proportion of time to foraging before, during, and after the rut. Our results showed that during the rut males also reduced lying time, while the ratio of time spent feeding to time spent lying did not change for males among periods. In conclusion, during the breeding season males maximized energy intake when not actively engaged in mating activities and rut‐induced hypophagia appeared to result from time budget constraints generated by mating‐related activities. Accordingly, the foraging constraint hypothesis seems appropriate to explain this phenomenon in Alpine ibex males.     

Liver total lipids and fatty acid composition of shot red and fallow deer males in various reproduction periods

In this study total lipid (TL) content and the fatty acid composition changes in the liver of red deer stags (n=35) and fallow deer bucks (n=19) were examined at various reproductive stages. Samples were taken from mature red deer stags in the rut (September), in the post-rut (October), at the end of the rut (November) and after sexual activity had ceased (January). Sampling from mature fallow bucks was performed in the pre-rut (early October), in the rut (November) and after the reproduction period (January). The results obtained indicated significant (P<0.001) fatty degeneration of the liver in the males at the rutting season. At that time the TL concentration (x+/-S.D. in wet weight) was 156+/-40 g/kg in the red deer stags and 405+/-46 g/kg in the fallow bucks. Subsequent to the rutting season this value decreased to 47+/-15 g/kg by November in the red deer stags and to 51+/-3 g/kg by January in the fallow bucks. Significant changes were also observed in the fatty acid composition of the liver lipids, determined by gas chromatography. Liver samples collected during the rutting season from both red deer stags and fallow bucks showed higher (P<0.001) total proportions of monounsaturated fatty acids and lower (P<0.001) weight percentages of polyunsaturated fatty acids than those taken in January. In comparison with January the liver samples taken in September from red deer stags showed significantly higher (P<0.001) proportions of fatty acids C14:0, C15:0 and C:16:1, and significantly lower (P<0. 001) proportions of C18:0, C20:4 (n-6) and C22:5 (n-3). The proportions of C14:0, C15:1, C17:1 and C18:3 (n-3) in the liver samples taken in November from fallow bucks were higher (P<0.001), while the proportions of C18:0 and C20:4 (n-6) were lower (P<0.001) than those measured prior to rutting (in October) or after the rut (in January).     

Red deer females collect on male clumps at mating areas

Mating strategies in mammalian herbivores are adapted to thedispersion of females, and female dispersion is mainly determinedby resource dispersion, although it is frequently unclear whetherfemales may also be influenced by the location of males. Inthe red deer (Cervus elaphus) the distribution of females beforethe rut predicts the places were males should establish territoriesand even their relative success. However, the number of femalesusing the mating areas in Doñana increases during therut. We observed 20 areas of meadows, used by grazing femalesbefore the rut. At the onset of the rut, the number of females increasedin some of these areas and decreased in others, and the opposite patternwas found after the rutting period. Changes in the vegetationat mating and nonmating areas could not account for the changesin female distribution; even some of the highest quality meadowswere vacated by females during rut. In selecting the matingareas, females avoided isolated small meadows within the scrubarea and preferred larger meadows where a number of neighboringrutting males could be found. Females also avoided those areas heavilyused by fallow deer (Dama dama), a competing sympatric species.We found that females suffered less sexual harassment when inlarger harems and when their harem was surrounded by other harems.Our results, together with those in the literature about thispopulation, indicate that red deer females collect during theearly rut in mating areas containing several rutting males,although once there they may select particular sites based on availabilityof food rather than based on the presence of a particular male. Byjoining harems in large meadows they are less harassed, andat the same time they probably increase their chances of matingwith highly competitive males. The results from Doñanasupport the idea that harassment avoidance may lead to femalemovements to areas with male territories without lek breedingor female comparison of male phenotypes and may bring an insightinto those factors leading to clumps of male territories andleks.     

Feeding or Resting? The Strategy of Rutting Male Alpine Chamois

Optimal foraging theory suggests that animals normally maximize energy intake to optimize their energy balance. However, when efficiency to assimilate energy falls below the level necessary to ascertain basal energetic requirements, they should shift to an energy saving strategy. Males of many ruminant species considerably reduce their food intake during the rut. Nevertheless, they are commonly assumed to maximize energy intake besides their investments in rutting activities. Based on predictions of optimal foraging theory and the specific ruminant digestive physiology, we propose, however, that rutting males in polygynous species with time consuming mating tactics should instead use an energy saving strategy. Particularly, we predict this to be the case in Alpine chamois (Rupicapra rupicapra rupicapra), a highly polygynous mountain ungulate, of which the males defend mating territories during the rut. By combining observational and telemetry data of eight radio‐collared males we constructed individual 24‐h time budgets, and compared the behavior of males before, during and after the rut. Males spent significantly less time feeding during the rut (0.9 h) compared with before (8.5 h) and afterwards (6.4 and 7.5 h, respectively), whereas time spent lying remained more or less unchanged (pre‐rut; 12.7 h, rut; 13.3 h, post‐rut; 12.9 and 13.9 h, respectively). The ratio of time spent feeding to lying dropped from 0.67 in the pre‐rut period to 0.05 in the rutting period. As a result, males allocated on average approx. 90% of their non‐rutting time to lying, and a negative relationship between rutting and lying time emerged. Hence, males seemed to trade lying time against rutting time. We conclude from these results that male Alpine chamois do not maximize their energy intake during the rut, but rather adopt an energy saving strategy to optimize their energy balance.     

不同发情阶段雄性鹅喉羚的时间分配特征

以往研究表明受发情交配行为制约,一些雄性反刍动物在发情期食物摄入量明显降低。已有两个相关假说解释该现象:能量摄入最大化假说和能量保存假说。作者于2009 ～ 2010 年在卡拉麦里山有蹄类自然保护区研究了雄性鹅喉羚不同发情阶段的时间分配。结果表明雄羚发情期采食时间比例明显下降(37. 9% ),低于发情前期(63. 6% )和发情后期(65. 8% );发情期卧息时间比例(6. 0% )与发情后期相近(5. 4% ),明显低于发情前期(23.2% );发情前期至发情后期采食卧息时间比(分别为2. 7、6. 3、12. 1)显著增加;发情期雄羚站立和移动时间比例明显升高,采食行为时间占非发情行为时间主要部分(86. 4% ),且采食行为与发情行为显著相关。相比之下,雌羚不同发情阶段采食行为时间分配比例相似。总之,除必需投入的发情行为外,发情期雄羚最大化其能量摄入;发情行为的投入是导致发情期雄羚食物摄入量下降的主导因子,雄性能量摄入最大化假说更好地解释了发情期鹅喉羚所采取的能量策略。     

Male red deer (<Emphasis Type="Italic">Cervus elaphus</Emphasis>) dispersal during the breeding season

Breeding dispersal can be of significant ecological and evolutionary importance. Yet, it is seldom considered in mammals. I present data on male red deer (Cervus elaphus) movements between sub-populations in southern Sweden during the rut. I investigated whether these movements could be breeding dispersal driven by mate competition. During the ruts of 1998–2009, I recorded 91 movements of males. The longest movement distance was 18.5 km. Dispersal was not restricted to yearlings or sub-adults, but also observed among adult stags. Of 91 movements observed, 7 were made by yearlings, 46 by sub-adults and 38 by adults. There was a significant move among yearlings and sub-adults towards areas with a higher ratio of females/adult males and towards areas with more females. The movements between rutting areas thereby seemed driven by sexual competition.     

Season effect on genitalia and epididymal sperm from Iberian red deer, roe deer and Cantabrian chamois

Seasonality deeply affects the physiology and behavior of many species, and must be taken into account when biological resource banks (BRBs) are established. We have studied the effect of seasonality on many reproductive parameters of free-ranging Iberian red deer, roe deer and Cantabrian chamois, living in Spain. Testicles from hunted animals were collected and sent to our laboratory at different times during the year. We recorded the weight and volume of testis, the weight of the epididymis and its separate parts (caput, corpus, and cauda), the weight of the sperm sample collected from the cauda epididymis, and several sperm parameters (sperm concentration, spermatozoa recovered, motility, HOS test reactivity, acrosomal status, and viability). We studied the data according to several periods, defined accordingly to each species. For red deer, we defined rut (mid-September to mid-October), post-rut (mid-October to mid-December), and non-breeding season (February). For roe deer, they were pre-rut (June), rut (July), post-rut (first fortnight of August), and non-breeding season (September). For chamois: non-breeding season (June to mid-September) and breeding season (October-November). The rut/breeding season yielded significantly higher numbers for almost all parameters. However, in the case of red deer, sperm quality was higher in the post-rut. For roe deer, testicular weight was similar in the pre-rut and in the rut, and sperm quality did not differ significantly between these two periods, although we noticed higher values in the rut. In the case of chamois, sperm quality did not differ significantly from the breeding season, but data distribution suggested that in the non-breeding season there are less males with sperm of good quality. On the whole, we find these results of interest for BRB planning. The best season to collect sperm in this species would be the breeding season. However, post-rut in red deer, pre-rut in roe deer, and non-breeding season in chamois could be used too, because of the acceptable sperm quality, despite the lower quantity salvaged. More in-depth research needs to be carried out on the quality of sperm salvaged at different times of the year in order to confirm these findings.     

The timing of male reproductive effort relative to female ovulation in a capital breeder

1. In large herbivores, the timing of breeding is important for females to hit peak plant protein levels. For males, the timing of reproductive effort is important to maximize the number of females they can mate during autumn rut in competition with other males. The latter depends on when most females are ovulating, but also on how other males with a different competitive ability are timing use of their capital (fat); it may pay younger males to invest more heavily later when prime aged males are exhausted. 2. Based on estimates of body mass loss, we quantify how much timing (start, peak and end dates) of male reproductive effort during rutting varies depending on male age, density and climate as well as timing of female ovulation. 3. Ovulation in adult females was delayed by 5 days from low to high density, and ovulation was also more synchronous at high density. The starting date of decline in male body mass was only later in yearlings than among other age groups. However, at low density, peak and end dates of rut became increasingly earlier and close to peak female ovulation with increasing age up to 7 years of age. Prime-aged males matched peak effort closely with peak rate of prime-aged female ovulation, while younger males were delayed. This is consistent with the view that younger males have a better chance when the prime-aged males are becoming exhausted. 4. Apart from yearlings, male age groups were synchronized in both the starting, peak and end dates of mass decline at high density. Thus, this partly follows change in female ovulation patterns, but also suggests that competition among males decreased with increasing density due probably to lower intensity of sexual selection. The lowered sexual selection may be due not only to more synchronous female ovulation, but also increasingly female-biased sex ratios and a younger male age structure with increasing density. 5. The onset of rutting is somewhat independent of male age (apart from the youngest males), but the peak and end of rutting effort is dependent strongly upon age, density and peak female ovulation. Male rutting phenology is thus best interpreted as a compromise between hitting peak female ovulation and intensity of sexual selection.     

Rut-Induced Hypophagia in Male Bighorn Sheep and Mountain Goats: Foraging Under Time Budget Constraints

In polygynous ungulates, the rut imposes constraints on male time budgets that generate a trade‐off between maintenance and reproduction, leading to a reduction in time spent foraging. As mating activities can incur substantial somatic costs, males are expected to spend their ‘non‐rutting’ time recovering during the breeding season. If the diminution in time allocated to foraging by males is only a consequence of time budget constraints, males should keep a similar ratio of time spent foraging to lying to that observed in the pre‐rut, leading to an overall reduction of these two activities (the ‘foraging constraint’ hypothesis). Alternatively, if males adopt an energy‐saving strategy, they should limit energy expenditures by reducing foraging but not lying time, as the energy gains of forage intake may not meet the basal energetic requirements, especially in northern and temperate regions (the ‘energy‐saving’ hypothesis). Here, we contrast these two hypotheses by comparing individual daily time budgets of marked adult bighorn sheep rams (Ovis canadensis) and male mountain goats (Oreamnos americanus) during the pre‐rut and the rut. Concordant results for both species support the ‘foraging constraint’ hypothesis, as sexually‐active males reduced time spent foraging and lying from the pre‐rut to the rut because of an increase in time spent in mating‐related activities. Bighorn sheep rams also increased time spent foraging when not engaged in mating tactics, providing further support for a ‘maximisation’ of energy intake in the absence of reproductive opportunities. Because there are also known physiological changes that occur during the rut which may cause appetite suppression, for example to produce metabolic compounds linked with olfactory communication (the ‘scent‐urination’ hypothesis) or to cope with increased burden of parasites (the ‘parasite‐induced anorexia’ hypothesis), further research should aim at simultaneously testing these current hypotheses to better understand rut‐induced hypophagia and its effects on the life histories of male ungulates.     

Fighting Tactics of Fallow Bucks (Dama dama,Cervidae): Reducing the Risks of Serious Conflict

Competition between male fallow deer (Dama dama), during the breeding season was studied to determine if conflict strategies were consistent with the reduction of risk. Agonistic interactions between males were analysed in relation to age, dominance rank and availability of mating opportunities. The breeding season was divided into two main periods: the pre-rut began when all males had cleaned the velvet from their antlers and ended on the last day before matings were first observed, while the rut refers to the period between the first and last matings. Overall, socially mature males (≥4yr old) were involved in more interactions than immature (≤3yr old) males. Males established dominance rank largely by non-contact agonistic interactions during the pre-rut and there was substantial carry-over of rank to the rut, when it was correlated with mating success. The mating success of males was skewed; mature males achieved 99.4% of the matings and immature males accounted for 0.6%. A mature male was 13 times more likely to fight than an immature male; the mature males that fought most often did so between 0.4 and 0.5 times per hour. During the rut, the number of fights was positively correlated across days with the number of matings. The majority of agonistic interactions (79%) comprising dyads of immature males, involved antler contact. In contrast, mature males engaged antlers in only 42% of their interactions. Fights between mature males lasted more than twice as long as those between immature males and were more likely to occur between opponents with similar dominance ranks. However, towards the end of the rut formerly mismatched opponents were more likely to fight. Thus males operated conditional competitive strategies to decide when to interact and fight. The persistence of rank order from the pre-rut period to the rut and the tendency for mature males to resolve disputes without antler contact, served to reduce the frequency of fights and therefore the risk of serious injury.     

不同年龄雄性北山羊发情期时间分配特征

前人研究表明,可多次繁殖的反刍物种其雄性个体在发情期采食时间显著减少。目前有两个假说解释这一现象,即能量摄入最大化假说和能量保存假说。为验证雄性北山羊在不同发情阶段所采取的能量保存策略,作者于2014年10-12月在新疆天山中部采用焦点动物取样法采集数据,采用Kruskal-Wallis检验和Spearman秩相关性检验分析数据。研究发现雄性北山羊成体和亚成体发情期采食时间均显著低于发情前期和发情后期,但二者在不同发情阶段卧息时间无显著变化,发情期采食和卧息时间比亦显著降低。发情期发情行为时间显著高于发情前期和发情后期,非发情时间主要用于采食。发情期采食时间和卧息时间都与发情行为时间呈显著的负相关关系。雌性北山羊发情期采食时间亦显著低于发情前期和发情后期,发情期和发情后期卧息时间显著高于发情前期。本研究结果表明,发情期不同年龄阶段雄羊都主要采取能量摄入最大化策略,但同时也具有部分能量保存策略的特征。     

Population dynamics and resource use of red deer after release from harvesting in New?Zealand

Despite periods of extensive government-funded control, fluctuating commercial exploitation and ongoing recreational hunting, little is known about how red deer (Cervus elaphus scoticus L?nnberg) in New?Zealand respond to the cessation of harvesting in terms of population growth rate and resource use. We describe the population dynamics and resource use of red deer in a montane catchment over 5?years (1962?67) following cessation of intensive government-funded control in 1961. Locations and sex?age classes of deer were observed monthly along a fixed route in the Harper-Avoca catchment, inland Canterbury. A total of 2036 red deer groups were observed. The number of groups observed annually increased during the study but no trends in median (2 or 3) or modal (1 or 2) group sizes were found. Population growth rates (r) of deer were extraordinarily high in the first two years (e.g. 2.33 ? 0.22 for adult females and 1.61 ? 0.23 for adult males), but decreased in subsequent years and were not biologically possible without substantial immigration and/or changes in detectability of deer. Sexual segregation and selection of vegetation types (alpine grassland, montane grassland, and forest) and 10 topographic landforms showed stronger intra-annual than inter-annual patterns. Segregation was greatest in spring and summer, least in the rut, and variable in winter. In all seasons, sexual segregation was greatest at 25- and 50-ha scales, moderate at 100-ha, and absent at the 500- and 1000-ha scales. Selection of vegetation types also varied seasonally, with deer of both sexes preferring montane grasslands in spring and summer and alpine grasslands in the rut. Backslopes were preferred landforms in spring and summer, spurs during spring and the rut, and hollows during the rut. Our results highlight the need to consider spatial scale, immigration, and detectability in the design of red deer culling and harvesting programmes. Studies of home-range size and use, migration patterns, dispersal rates and distances are required to better understand the impacts of red deer on New?Zealand ecosystems and the effects of management on red deer populations.     

Contrasting Alternative Hypotheses to Explain Rut‐Induced Hypophagia in Territorial Male Chamois

Male ungulates in temperate environments often show a severe reduction in time spent foraging during the mating season. Several hypotheses have been put forward to explain this phenomenon but, so far, no study investigated the proximate mechanisms underlying rut‐induced hypophagia in ungulates using alternative mating tactics (AMTs). Between the pre‐rut and post‐rut of 2011 and 2012, we collected data on activity budgets, parasite burden and androgen levels of territorial and non‐territorial male Alpine chamois Rupicapra r. rupicapra in the Gran Paradiso National Park (Italy). We aimed to investigate whether AMTs showed similar reduction in time spent foraging during the mating period and to test the predictions underlying alternative hypotheses that may explain rut‐induced hypophagia. Only territorial males showed a significant reduction in time spent foraging during the rut; the lack of correlation between proportion of time spent foraging and androgen metabolites or parasite burden did not fully support the physiological and the parasite hypotheses, while the foraging constraint, the energy‐saving and the physical rest hypotheses could not be discounted. Territorial males decreased the time spent lying down from the pre‐rut to the rut, but not their foraging‐to‐lying‐down ratio. During the mating period, we found negative correlations between time spent foraging or lying down and time spent rutting. Our data suggest that territorial males’ behaviour is more consistent with the foraging constraint hypothesis than with the energy‐saving hypothesis previously suggested. Yet, during the rut territorial males did not maximise their foraging time, and the optimisation of their energy balance could rather depend upon feeding on relatively high‐quality plants. This suggestion – possibly named ‘forage quality hypothesis’ – now requires further investigations. This work showed that alternative mating behaviours may underlie different patterns of foraging strategies: we suggest that tests of alternative hypotheses to explain rut‐induced hypophagia within ungulate populations should not ignore the occurrence of AMTs.     

A new sexual signal in rutting male red deer: Age related chemical scent constituents in the belly black spot

Rutting behaviour of red deer stags (Cervus elaphus) includes an extensive repertoire of visual and acoustic signals directed either to rival males or to females. As in other mammals, olfactory communication is expected to play a central role in these rutting interactions too, but this has rarely been investigated. Only during the rutting season, red deer males show a conspicuous black spot area throughout most of their underbelly produced by the impregnation of substances with a strong scent. Here, we examined the origin of these compounds and their potential role as chemical signals. By using gas chromatography–mass spectrometry (GC–MS), we identified 67 compounds in the hair from the belly black spot of red deer stags, mainly heterocyclic aromatic organic compounds, such as m-cresol, benzoic acid, cyclohexanecarboxylic acid and ethylphenol, but we also found steroids, such as cholesterol and androstane-3,17-dione, carboxylic acids and their esters between n-C₆ and n-C₂₂, alcohols, squalene and other minor compounds. Many of these compounds are found in the belly black spot but not in other hair areas, and may have originated from several sources, such as the urine or the sebaceous glands of the skin, which impregnated the belly. Moreover, we found differences in chemical profiles depending on age, with older males having higher proportions of benzoic acid and androstane-3,17-dione, but lower proportions of m-cresol. Because most of these compounds are strongly odoriferous, and appear related to male characteristics, our data indicate that scent from the hairs forming the black spot of the belly may be regarded as an overlooked new sexual chemical signal in red deer in the context of competition for mates during the rutting season.     

Ranging behaviour and excursions of female roe deer during the rut

Anecdotal evidence has suggested that, during the rutting period, female roe deer may undertake short excursions, outside of their normal home range, possibly to mate with a reproductive partner. To address this question, we analysed the ranging behaviour of 27 female roe deer Capreolus capreolus, equipped with GPS collars, inhabiting a fragmented landscape in France. We compared female movements during the rutting period with a non-rutting period over two summers using a recently published approach. Search intensity and home range size were significantly greater during the rutting period. The difference in home range size between the two periods was significantly greater in 2006 compared to 2005 and in open compared to closed habitat. We were not able to identify any influence of body mass on the difference in ranging behaviour between the two periods. Visual analysis of movement trajectories for 11 females revealed that 5 (45%) performed an excursion for a duration of a few hours to several days. We speculatively suggest that female rut excursions provide an opportunity for active mate choice in roe deer, where males are territorial, although we cannot rule out the alternative explanation that these movements are a means to avoid male harassment.     

内蒙古达赉湖地区蒙原羚繁殖期及其前后昼间行为时间分配及能量平衡策略

2007年11月、12月和2008年3月,在内蒙古达赉湖地区,采用扫描取样法对雌雄蒙原羚繁殖期及其前后昼间行为时间分配进行了研究。 研究表明：（1）繁殖期前、繁殖期和繁殖期后,雌性蒙原羚采食时间,占昼间活动时间的比例分别为（44.9±3.8）%、（43.5±4.0）% 和 (46.2±3.1)%;卧息时间,占昼间活动时间的比例分别 为（32.3±4.8）%、（29.2±2.9）% 和 (28.0±4.8)%;雌性蒙原羚在繁殖期及其前后采食、移动和卧息的行为时间分配差异不显著（P>0.05）,站立、繁殖、“其他”行为时间分配差异性显著（P<0.05）。（2）繁殖期前、繁殖期和繁殖期后, 雄性蒙原羚采食时间,占昼间活动时间的比例分别为 (52.6±3.8)%、(17.5±2.8)% 和 (29.8±4.8)%;卧息时间,占昼间活动时间的比例分别为 (13.4±6.4)%、(24.2±4.1)% 和 (44.2±4.7)%。雄性蒙原羚在繁殖期及其前后采食、卧息、站立、移动、繁殖、“其他”时间分配均有显著差异（P<0.05）。动物采食卧息的行为时间分配反映动物的能量平衡策略。雌性蒙原羚的时间分配表明,雌性蒙原羚的能量平衡策略在繁殖期前、繁殖期和繁殖期后没有发生显著变化,均为能量摄入最优化策略,尽可能多的时间分配在采食上;雄性蒙原羚的时间分配表明,在繁殖期前,其能量平衡策略为能量摄入最优化策略,尽可能多的时间分配在采食上;雄性蒙原羚繁殖期及繁殖期后其能量平衡策略转变为能量支出优化策略,尽可能少的支出能量,尽可能多的时间分配在卧息上。