Reconstructing the reproductive history of female polar bears using cementum patterns of premolar teeth

Premolar teeth collected from 220 adult female polar bears (Ursus maritimus) from western Hudson Bay, Canada, were examined to determine whether past reproductive events are recorded in cementum. The widths of annular cementum growth layer groups (GLGs) were measured and compared as proportional width index (PWI) values to correct for age and body size bias. Known reproductive states (pregnant, with cubs, or with yearlings) were used to confirm and calibrate cementum annuli. Significant differences in PWI were observed between GLGs formed the year females were pregnant versus when accompanied by cubs or yearlings. The probability of a female having produced a cub in adulthood was determined by fitting a logistic regression model between the ΔPWI of females when pregnant and with their cubs. Logistic regression of ΔPWI (β₀ = −0.229, β₁ = −13.465, G ² = 46.55, df = 1, P < 0.001) correctly classified the presence or absence of cubs in 72% of GLGs. Cementum width did not vary between different litter sizes. Observations of females with early litter loss suggests that longer periods of lactation contributes to decreased cementum width and therefore cementum may record a minimum age of litter survival. Predictions of litter production rate (0.43 litters/female/year) derived from cementum were similar to field observations; however, age at first parturition was underestimated by 1 year. We conclude that patterns of cementum deposition may be useful to determine individual reproductive histories and establish course estimates of reproductive parameters when regular field observations are not feasible. We also conclude that reproductive parameters derived from cementum are not adequate on their own for monitoring populations which are in decline or under stress and field observation should not be replaced under these conditions.     

What lies beneath? Population dynamics conceal pace‐of‐life and sex ratio variation,with implications for resilience to environmental change

Life‐history and pace‐of‐life syndrome theory predict that populations are comprised of individuals exhibiting different reproductive schedules and associated behavioural and physiological traits, optimized to prevailing social and environmental factors. Changing weather and social conditions provide in situ cues altering this life‐history optimality; nevertheless, few studies have considered how tactical, sex‐specific plasticity over an individual's lifespan varies in wild populations and influences population resilience. We examined the drivers of individual life‐history schedules using 31 years of trapping data and 28 years of pedigree for the European badger (Meles meles L.), a long‐lived, iteroparous, polygynandrous mammal that exhibits heterochrony in the timing of endocrinological puberty in male cubs. Our top model for the effects of environmental (social and weather) conditions during a badger's first year on pace‐of‐life explained <10% of variance in the ratio of fertility to age at first reproduction (F/α) and lifetime reproductive success. Conversely, sex ratio (SR) and sex‐specific density explained 52.8% (males) and 91.0% (females) of variance in adult F/α ratios relative to the long‐term population median F/α. Weather primarily affected the sexes at different life‐history stages, with energy constraints limiting the onset of male reproduction but playing a large role in female strategic energy allocation, particularly in relation to ongoing mean temperature increases. Furthermore, the effects of social factors on age of first reproduction and year‐to‐year reproductive success covaried differently with sex, likely due to sex‐specific responses to potential mate availability. For females, low same‐sex densities favoured early primiparity; for males, instead, up to 10% of yearlings successfully mated at high same‐sex densities. We observed substantial SR dynamism relating to differential mortality of life‐history strategists within the population, and propose that shifting ratios of ‘fast’ and ‘slow’ life‐history strategists contribute substantially to population dynamics and resilience to changing conditions.     

Family Feuds: Severe Aggression among Cooperatively Breeding Cotton-Top Tamarins

A survey of severe aggression occurring over the 20 year history of a cotton-top tamarin (Saguinus oedipus) colony indicated that most aggression was between same-sex individuals, with fights among siblings more common than parent-offspring conflict. Males engaged in severe aggression more often than females did, paralleling the dimorphic aggressive response to same-sex intruders in this species. Female-female aggression occurred at larger group sizes than male-male aggression, suggesting a higher threshold for female aggression. Much sibling aggression was directed by postpubertal subadults toward prepubertal siblings. Only 17% of aggression occurred in association with infant births, and these cases rarely involved parents and offspring suggesting that aggression was not used by reproductive animals to defend their breeding position. Severe aggression was often associated with attempts to introduce stepparents or movement of individuals in and out of the group. The mean group sizes when aggression is observed in captivity are close to the maximum group sizes observed in wild tamarins, which suggests that severe aggression in captive groups may reflect processes related to dispersal in wild tamarins.     

Reproductive performance of the wild white-lipped peccary (<Emphasis Type="Italic">Tayassu pecari</Emphasis>) female in the Peruvian Amazon

The ability of any species to support high hunting pressures depends on its reproductive efficiency. Based on the gross anatomic examination of 208 adult female reproductive tracts, we characterised the reproductive biology of the wild white-lipped peccary in the northeastern Peruvian Amazon. White-lipped peccary apparently bred year round in the northeastern Peruvian Amazon, and the number of pregnant females was 80 (38.4%). Mean ovulation rate was 2.09 ± 0.47 CLs, and litter size was 1.60 ± 0.49 embryos or foetuses per pregnant female. A phenomenon of embryo migration was observed in the 27.5% of pregnant females. Estimations suggest 0.89 births per year and a yearly reproductive production of 1.42 piglets per pregnant female. Females in the late pregnancy stage showed a higher hunting vulnerability that could be an important restrictive factor for the reproductive efficiency of the wild white-lipped peccary populations in the Peruvian Amazon.     

Determinants of reproductive success in female Columbian ground squirrels

Summary We studied the reproductive success of female Columbian ground squirrels (Spermophilus columbianus) in southwestern Alberta for nine years. We defined reproductive success as the number of offspring surviving their first hibernation, classified as yearlings. The number of weaned juveniles explained one third of the variance in number of yearlings at emergence from their first hibernation the following spring, and much of the variance in individual reproductive success originated after weaning. Weight of adult females at emergence from hibernation was correlated with annual reproductive success. The mother's survival beyond weaning and the subsequent winter's snow accumulation had positive effects on annual reproductive success, whereas population density and summer temperature had negative effects. We found no effects on annual reproductive success of date of litter emergence, weight at emergence as a yearling, presence or absence of adult kin, distance from the natal site, location within the study area, winter temperature or summer precipitation. Age of first breeding did not affect lifetime reproductive success, which ranged from 0 to 19 yearlings produced over a lifetime. The greatest source of variation in lifetime reproductive success for females surviving to breeding age was offspring survival, followed by reproductive lifespan.     

Costs of reproduction in life history of a perennial plant <Emphasis Type="Italic">Carex secalina</Emphasis>

We tested a hypothesis based on life history theory that examines reproductive costs incurred by individuals in consecutive years of their life. A multi-year dataset of resource allocation to vegetative and reproductive structures was analysed in Carex secalina — a perennial, monoecious sedge, reproducing only sexually. In a four-year garden experiment, we assessed above-ground biomass at the end of each season and reproductive allocation expressed as the total length of male and female spikes. The study was aimed at determining how size and age of a plant relates to its reproduction, and how the rate of reproduction affects the year-toyear biomass change in Carex secalina. We observed that after each reproductive episode, individuals had significantly smaller sizes and produced a lower number of generative tillers. The total production of reproductive structures decreased significantly with age in all populations. Moreover, the decrease in plant biomass was greater when more reproductive structures were produced in a previous year, which indicates that the plants incur costs of reproduction in terms of above-ground biomass production.     

Reproductive parameters of the common genet <Emphasis Type="Italic">Genetta genetta</Emphasis> (Linnaeus, 1758) in Southwest Europe

We used information from 148 litters belonging to 119 different wild and captive female common genets (Genetta genetta) in SW Europe over a period of almost 50 years to study certain reproductive parameters. Data were obtained from a combination of sources including carcasses, live captures, telemetry-based studies, captive genets, and reports in the literature. The circannual pattern of breeding was fairly similar in both wild and captive genets, with births occurring in all months except December, albeit with a large peak in spring and a secondary peak in autumn. The sex ratio at birth was near to 1:1, and mean litter size was 2.16 ± 0.76 cubs/litter with a range of 1–5 cubs. Litters of two cubs were the most frequent both in wild and captive settings. In captivity, we have observed the births of replacement litters and double litters; however, we did not find evidence of wild females that having two litters in the same year. We conclude that the possibility of breeding at any time of the year is facilitated by the continuous spermatogenesis of the males and by the ability of females to enter into estrus after losing a litter prematurely and to breed twice in the same year.     

Mechanisms and reproductive consequences of breeding dispersal in a specialist predator under temporally varying food conditions

Individual variation in breeding dispersal has extensive ecological and evolutionary consequences, but the factors driving individual dispersal behaviour and their fitness consequences remain poorly understood. Our data on dispersal events of a rodent‐specialist predator, the Eurasian kestrel Falco tinnunculus, over 20 years in western Finland offers a unique opportunity to explore the mechanisms underlying breeding dispersal behaviour and its reproductive consequences in a wild bird population. Sex, age, body condition and previous breeding success affected breeding dispersal. Dispersal distances were longer in females than in males as well as longer in yearlings than in older individuals. Body condition was positively correlated to breeding dispersal distances, particularly for females. The lowest dispersal distances were recorded for intermediate brood sizes in the year preceding dispersal. Our results highlight sex‐ and environment‐specific consequences of breeding dispersal on reproductive performance. During increase phases of the three‐year vole cycles, males dispersing further had lower reproductive performance after dispersal, whereas in females, long breeding dispersal distances were associated with increased breeding success under all environmental conditions. These results suggest benefits associated to breeding dispersal in females, potentially related to large spatio‐temporal variation in main food abundance and intensity of intra‐specific competition. Breeding dispersal of males was costly during increasing food abundance, indicating the potential fitness benefits of environmental familiarity in this migratory species. Overall, our results indicate that both individual traits and environmental factors interact to shape breeding dispersal strategies in wide‐ranging predator populations under fluctuating food conditions.     

Spermatozoan numbers and characteristics of associated organs in male white-tailed deer during the breeding season

Short-term changes in testicular spermatozoa, testes weight, testes length, epididymes weight, epididymal spermatozoa, and body weight of adult and yearling male white-tailed deerOdocoileus virginianus (Zimmermann, 1780) were examined over a 9-week period that included the peak of the breeding season in South Carolina. Mean values for all characteristics were significantly greater in adults compared to yearlings. Values for reproductive characteristics tended to be highest during the last week in October or the first week in November and decreased over the course of the investigation. Body weight of adults decreased from late October through early December, whereas body weight of yearlings fluctuated only slightly throughout the 9-week period. Significant correlations were observed among all reproductive characteristics and body weight was highly correlated with all characteristics except testicular spermatozoa. Values for reproductive characteristics differed significantly between the right and left sides of the reproductive tracts. Results demonstrate the occurrence of short-term changes in reproductive capabilities of white-tailed deer that are relevant for the development of management strategies for this species.     

Reproductive biology and management of captive black-footed ferrets (Mustela nigripes)

A captive breeding program is being conducted with black-footed ferrets (Mustela nigripes), an endangered species. Results of 5 years of study are reported. Simple, but specialized, nontraumatic handling techniques allowed assessment of reproductive status with minimal stress, which was important in breeding management. Black-footed ferrets are sexually mature and may successfully reproduce in their 1st year. Proestrus lasts approximately 2-3 weeks. Duration of estrus in unbred females was 32–42 days; females usually bred within 20 days. Most breeding activity occurred during April. Mean gestation length was 42.7 days (±0.7, range 42–45 days), litter size averaged 3.0 kits (±1.4, range 1–6 kits), and weaned kits/litter averaged 2.4 (±1.7, range 1–6 kits). Weaning rate of kits was 80%. Sex ratio of kits was essentially 1:1. Productivity was greatest among females ?3 years of age. Rapid expansion of the captive population is possible and will be important for genetic management of the species and for achieving the primary goal of the recovery program, which is to return black-footed ferrets to the wild.     

Reproductive parameters of wild boar (<Emphasis Type="Italic">Sus scrofa</Emphasis>) in three different parts of Germany

Recent increases in wild boar populations in central Europe necessitated an evaluation of the current reproductive performance of this species. During a 2-year study, samples of ovaries and uteri were taken from wild boars from areas in the (northern) state of Lower Saxony and the (more southern) Rhineland-Palatinate, Germany, in which wild boar have been vaccinated against classical swine fever (CSF) after several outbreaks of the disease. Serum samples were also analyzed to determine the prevalence of diseases that may influence pig reproduction and fertility. While there was a striking seasonality of reproductive performance, especially among older animals, mating was delayed in up to 15% of piglets and yearlings, leading to a second peak of farrowing from June to August. Depending on the area, between 60 and 70% of the piglets were most likely to become pregnant during the main period of reproduction, while another two thirds of the remaining individuals farrowed by the summer, which was the case in the mountainous areas. The arithmetic mean number of fetuses were 6.29 per piglet, 6.67 per yearling, and 7.64 per adult for wild boar in Eastern Lower Saxony; 4.58 per piglet and 4.63 per yearling and 6.56 per adult for wild boar in the Western Eifel and 4.77 per yearling and 6.50 per adult in the Palatine Forest, as the number of pregnant piglets has been too low to calculate an arithmetic mean in this area. The numbers of Lower Saxony wild boar fetuses per individual exceed previously known values. The results indicate that exogenous factors have a strong impact on both reproductive seasonality and the percentage of reproducing individuals in an age group. Ovulation rates, numbers of fetuses, and prevalence of pregnancies were found to be high among all age groups, while early onset of puberty and high pregnancy rates were typical of young animals (yearlings). The influence of some important reproductive diseases like Aujeszky’s disease, Brucellosis, porcine reproductive and respiratory syndrome, porcine parvovirosis, and CSF on wild boar reproduction and fertility was tested and found to be at least of minor interest for the reproductive outcome of the species.

Reproductive biology,multiple paternity and polyandry of the bull shark Carcharhinus leucas

To improve understanding of bull shark Carcharhinus leucas reproductive biology, we analysed reproductive traits from 118 bull sharks caught along Reunion Island coasts (Western Indian Ocean), including 16 gravid females. Specific microsatellite loci were used to investigate the frequency of multiple paternity. Males and females reached maturity at c. 234 cm and 257 cm total length (L_T), respectively, and litter sizes ranged from 5 to 14 embryos. Analysis of the 16 litters collected in various months of the year indicated that parturition occurs between October and December, with a size at birth c. 60–80 cm L_T and that the gestation period is probably c. 12 months. Assuming a 1 year resting period and a period of sperm storage (4–5 months) between mating (in June–September) and fertilisation, the reproductive cycle of bull sharks at Reunion Island would be biennial. At least 56.25% of the litters investigated were polyandrous, sired by 2–5 males. Several males that each sired several litters conceived during the same or distinct mating seasons were detected, suggesting both a seasonal aggregation of sharks to mate and some male fidelity to mating site. Altogether, these findings provide valuable information for both shark risk management and conservation of the species in the Western Indian Ocean.     

Reproductive and post‐reproductive life history of wild‐caught Drosophila melanogaster under laboratory conditions

The life history of the fruit fly (Drosophila melanogaster) is well understood, but fitness components are rarely measured by following single individuals over their lifetime, thereby limiting insights into lifetime reproductive success, reproductive senescence and post‐reproductive lifespan. Moreover, most studies have examined long‐established laboratory strains rather than freshly caught individuals and may thus be confounded by adaptation to laboratory culture, inbreeding or mutation accumulation. Here, we have followed the life histories of individual females from three recently caught, non‐laboratory‐adapted wild populations of D. melanogaster. Populations varied in a number of life‐history traits, including ovariole number, fecundity, hatchability and lifespan. To describe individual patterns of age‐specific fecundity, we developed a new model that allowed us to distinguish four phases during a female's life: a phase of reproductive maturation, followed by a period of linear and then exponential decline in fecundity and, finally, a post‐ovipository period. Individual females exhibited clear‐cut fecundity peaks, which contrasts with previous analyses, and post‐peak levels of fecundity declined independently of how long females lived. Notably, females had a pronounced post‐reproductive lifespan, which on average made up 40% of total lifespan. Post‐reproductive lifespan did not differ among populations and was not correlated with reproductive fitness components, supporting the hypothesis that this period is a highly variable, random ‘add‐on’ at the end of reproductive life rather than a correlate of selection on reproductive fitness. Most life‐history traits were positively correlated, a pattern that might be due to genotype by environment interactions when wild flies are brought into a novel laboratory environment but that is unlikely explained by inbreeding or positive mutational covariance caused by mutation accumulation.     

Life‐history traits of the long‐nosed skate Dipturus oxyrinchus

This work investigates life‐history traits of the long‐nosed skate Dipturus oxyrinchus, which is a common by‐catch in Sardinian waters. The reproductive variables were analysed from 979 specimens sampled during scientific and commercial hauls. Females (10·4–117·5 cm total length, L_T) attained larger sizes than males (14·5–99·5 cm L_T). To evaluate age and growth, a sub‐sample of 130 individuals (76 females and 54 males) were used. The age was estimated by annuli counts of sectioned vertebral centra. Four models were used for the length‐at‐age data: the von Bertalanffy, the exponential, the Gompertz and the logistic functions. According to the Akaike's information criterion, the Gompertz model seemed to provide the best fitting curve (L_∞ mean ± s.e. : 127·55 ± 4·90 cm, k: 0·14 ± 0·09, IP: 3·97 ± 0·90 years). The oldest female and male were aged 17 (115·5 cm L_T) and 15 years (96·0 cm L_T), respectively. Lengths at maturity were 103·5 cm for females and 91·0 cm for males, corresponding to 90% of the maximum observed length in both sexes. The monthly distribution of maturity stages highlighted an extended reproductive cycle, with spawning females and active males being present almost throughout the year, as confirmed by the gonado‐somatic index. Ovarian fecundity reached a maximum of 26 yolked follicles with a mean ± s.e. size of 19·7 ± 6·5 mm.     

Testing the reproductive and somatic trade‐off in female Columbian ground squirrels

Energetic trade‐offs in resource allocation form the basis of life‐history theory, which predicts that reproductive allocation in a given season should negatively affect future reproduction or individual survival. We examined how allocation of resources differed between successful and unsuccessful breeding female Columbian ground squirrels to discern any effects of resource allocation on reproductive and somatic efforts. We compared the survival rates, subsequent reprodction, and mass gain of successful breeders (females that successfully weaned young) and unsuccessful breeders (females that failed to give birth or wean young) and investigated “carryover” effects to the next year. Starting capital was an important factor influencing whether successful reproduction was initiated or not, as females with the lowest spring emergence masses did not give birth to a litter in that year. Females that were successful and unsuccessful at breeding in one year, however, were equally likely to be successful breeders in the next year and at very similar litter sizes. Although successful and unsuccessful breeding females showed no difference in over winter survival, females that failed to wean a litter gained additional mass during the season when they failed. The next year, those females had increased energy “capital” in the spring, leading to larger litter sizes. Columbian ground squirrels appear to act as income breeders that also rely on stored capital to increase their propensity for future reproduction. Failed breeders in one year “prepare” for future reproduction by accumulating additional mass, which is “carried over” to the subsequent reproductive season.     

Paternity in wild ring‐tailed lemurs (Lemur catta): Implications for male mating strategies

In group‐living species with male dominance hierarchies where receptive periods of females do not overlap, high male reproductive skew would be predicted. However, the existence of female multiple mating and alternative male mating strategies can call into question single‐male monopolization of paternity in groups. Ring‐tailed lemurs (Lemur catta) are seasonally breeding primates that live in multi‐male, multi‐female groups. Although established groups show male dominance hierarchies, male dominance relationships can break down during mating periods. In addition, females are the dominant sex and mate with multiple males during estrus, including group residents, and extra‐group males—posing the question of whether there is high or low male paternity skew in groups. In this study, we analyzed paternity in a population of wild L. catta from the Bezà Mahafaly Special Reserve in southwestern Madagascar. Paternity was determined with 80–95% confidence for 39 offspring born to nine different groups. We calculated male reproductive skew indices for six groups, and our results showed a range of values corresponding to both high and low reproductive skew. Between 21% and 33% of offspring (3 of 14 or three of nine, counting paternity assignments at the 80% or 95% confidence levels, respectively) were sired by extra‐troop males. Males siring offspring within the same group during the same year appear to be unrelated. Our study provides evidence of varying male reproductive skew in different L. catta groups. A single male may monopolize paternity across one or more years, while in other groups, >1 male can sire offspring within the same group, even within a single year. Extra‐group mating is a viable strategy that can result in extra‐group paternity for L. catta males.     

Time spent in distinct life history stages has sex‐specific effects on reproductive fitness in wild Atlantic salmon

In species with complex life cycles, life history theory predicts that fitness is affected by conditions encountered in previous life history stages. Here, we use a 4‐year pedigree to investigate if time spent in two distinct life history stages has sex‐specific reproductive fitness consequences in anadromous Atlantic salmon (Salmo salar). We determined the amount of years spent in fresh water as juveniles (freshwater age, FW, measured in years), and years spent in the marine environment as adults (sea age, SW, measured in sea winters) on 264 sexually mature adults collected on a river spawning ground. We then estimated reproductive fitness as the number of offspring (reproductive success) and the number of mates (mating success) using genetic parentage analysis (>5,000 offspring). Sea age is significantly and positively correlated with reproductive and mating success of both sexes whereby older and larger individuals gained the highest reproductive fitness benefits (females: 62.2% increase in offspring/SW and 34.8% increase in mate number/SW; males: 201.9% offspring/SW and 60.3% mates/SW). Younger freshwater age was significantly related to older sea age and thus increased reproductive fitness, but only among females (females: ?33.9% offspring/FW and ?32.4% mates/FW). This result implies that females can obtain higher reproductive fitness by transitioning to the marine environment earlier. In contrast, male mating and reproductive success was unaffected by freshwater age and more males returned at a younger age than females despite the reproductive fitness advantage of later sea age maturation. Our results show that the timing of transitions between juvenile and adult phases has a sex‐specific consequence on female reproductive fitness, demonstrating a life history trade‐off between maturation and reproduction in wild Atlantic salmon.     

Correlates and Consequences of Dominance in a Social Rodent

In harem‐polygynous societies, body condition is often correlated with dominance rank. However, the consequences of dominance are less clear. High‐ranking males do not inevitably have the highest reproductive success, especially in systems where females mate with multiple males. In such societies, we expect male reproductive success to be more highly skewed than female reproductive success, but reproductive skew in females can still arise from rankings established within matrilineal societies. Dominance can also impact life‐history decisions by influencing dispersal patterns in yearlings. To better understand the function of dominance in harem‐polygynous societies, we studied the causes and consequences of dominance in yellow‐bellied marmots (Marmota flaviventris), a social rodent with skewed male reproductive success and female reproductive suppression. Specifically, we examined body condition as a predictor and the probability of breeding, number of offspring, and dispersal as outcomes of dominance. Additionally, we looked at variation in dominance between males and females and adults and yearlings, because marmots can engage in distinct interactions depending on the type of individuals involved. We found that marmots in better body condition have higher dominance rank than those in poorer condition. In addition, adults are dominant over yearlings. Within yearlings, dominance does not influence dispersal, but those in better body condition are less likely to disperse. Within all adults, individuals in better condition produce more offspring per year. Within adult males, more dominant males have greater reproductive success. Despite previous evidence of reproductive suppression in females, we found no effects of dominance rank on female reproductive success in the current study. The function of dominance in female marmots remains enigmatic.     

Reproductive biology of captive female Eurasian lynx, Lynx lynx

Studies on wild Eurasian lynx (Lynx lynx) have revealed variation in reproduction between areas, years and individuals. In order to explore potential causes for this variation other than food supply, we analysed data from captive lynx, which provide conditions with minimal environmental variation as all were fed ad libitum. Data from 37 individual female lynx were available from 20 zoos in Norway, Sweden, Finland, Switzerland and the Czech Republic. Data on 177 reproductive events (where a male was available to the female at mating time) are presented. Of these events, 85% resulted in litters being born. Average litter size was 1.95, with a variation from 1 to 4. The mean birth date was 26th May, and sex ratio was not significantly different from parity. The probability of reproduction was related to age, with fewer litters produced by the very young (2–3-year old), and no sign of a senescence effect. However, a clear effect of senescence on litter size was evident. The captive lynx did not have higher reproductive rates than wild lynx, indicating that either factors other than food supply are driving the variation in wild lynx reproduction, or that a factor such as stress may be causing additional variation in the captive population.     

Home ranges and movement patterns in a vulnerable polecat<Emphasis Type="Italic">Mustela putorius</Emphasis> population

Home range characteristics and movement patterns of four female and six male polecatsMustela putorius Linnaeus, 1758 were studied in Luxembourg using radiotelemetry. Home range size of polecats ranged from 42 to 428 ha with an average of 181 ha. The mean (± SE) home range size of males of (246±45 ha) was significantly larger than that of females (84±17 ha). Polecats concentrated 50% of their space use in only 15% of their home range possibly indicating a patchy environment. Comparing our data with other studies in Europe, polecats seem to occupy approximately the same home range size (except in Switzerland) regardless of population density. Average distance traveled per night by males was 3.6 times greater than that of females. Also, seasonal variation in movements was observed in males but not in females.