Sex differences in olfactory social recognition memory in meadow voles,Microtus pennsylvanicus

Terrestrial mammals, like rodents, use odors, and scent marks to indicate their presence in an area to conspecifics. These odors convey information about the scent donor's genotype, sex, condition, and age. The ability to discriminate among the scent marks of conspecifics and later recollect the identity of the donor is essential for choosing between familiar and unfamiliar mates. We tested the hypothesis that the promiscuous meadow vole (Microtus pennsylvanicus) can recollect the odor of a familiar, opposite-sex conspecific and distinguish it from that of an unfamiliar, opposite-sex conspecific. We also hypothesized that because reproductive success is highly skewed among male meadow voles and competition for mates is intense, males will be more likely than females to recollect the odor of a familiar, opposite-sex conspecific and distinguish it from that of an unfamiliar, opposite-sex conspecific, for a longer period of time. Using a habituation task, we first exposed the voles, 4 times successively, to the anogenital area scent of an opposite-sex conspecific. Then, 1 hr, 24 hrs, 72 hrs, or 96 hrs after the fourth exposure, voles were presented with the odor of the donor from the exposure phase (familiar donor) and that of an unfamiliar, opposite-sex conspecific. Female meadow voles spent similar amounts of time investigating the scent of the familiar male donor and that of an unfamiliar male donor after the 1-hr and 24-hr intervals. Male meadow voles, however, spent more time with the scent of an unfamiliar female donor than that of the familiar female donor after the 1-hr, 24-hr, and 72-hr intervals, suggesting that male voles could recollect the scent mark of a familiar female for at least three days. The implications of these sex differences in social memory may reflect the different strategies male and female meadow voles use in the recognition of previous and potential mates. Recognition of an individual's scents may enhance fitness by allowing animals to direct appropriate behaviors toward those individuals.     

Mating system of the meadow vole, Microtus pennsylvanicus

Previous studies on parental and spacing behavior of Microtuspennsylvanicus suggest a promiscuous mating system, but attemptsto find multiple paternity in single litters have been unsuccessful.In this paper we present evidence of multiple paternity in singlelitters conceived in the wild early in the breeding season.The proportion of litters sired by multiple males was estimated,by a conservative method, to be 33.1%.We argue that the presenceof promiscuity, rather than polygyny, in M. pennsylvanicus isthe result of two factors. First, overwintered breeding malesare similar in age and size, resulting in small variation incompetitive ability among males. This reduced variation in competitiveability reduces the possibility that some males defend severalfemales and others defend none. Second, the habitat structureof the meadow vole makes it difficult for a male to detect othermales nearby, and this reduces the possibility that one maleexcludes others from mating when a female comes into estrus.     

Introduced cats Felis catus eating a continental fauna: inventory and traits of Australian mammal species killed

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Foods of feral house cats (Felis catus L.) in forest of the Orongorongo Valley,Wellington

Abstract

The foods of feral house cats in forest in the Orongorongo Valley, Wellington, were studied over 3 years and related to the availability of prey. Some cats were trapped, tagged, and released, and could be identified individually by coat colour and pattern. The number of cats, estimated from live-trapping and sightings, was stable during the study. Examination of 677 scats revealed that mammals (rat, rabbit, opossum, mouse, and stoat, in descending order of importance) formed the bulk of the diet by weight. Remains of birds occurred in 12% of scats, but birds were estimated to form only 4.5% by weight of the diet. Insect fragments were present in many scats; wetas (Orthoptera), cicadas (Hemiptera), and beetles (Colcoptera) were important seasonally. Although eaten in large numbers, they contributed very little by weight to the diet. Populations of rats, rabbits, and opossums were fairly stable during the study; mice were abundant for most of the first 18 months, but were scarce in the last year. The literature on the food habits of feral house cats is reviewed; it emphasises that cats are primarily predators of small mammals (rodents and lagomorphs). Predation by feral cats can be important in holding rat and rabbit populations at low densities and in reducing seasonal fluctuations in their numbers. Cats can also exert heavy predation pressure on low-density mouse populations. Although the cats now eat few birds, they may have been responsible for reducing the numbers of some forest birds in the past.     

Genetic analysis shows low levels of hybridization between African wildcats (Felis silvestris lybica) and domestic cats (F. s. catus) in South Africa

Hybridization between domestic and wild animals is a major concern for biodiversity conservation, and as habitats become increasingly fragmented, conserving biodiversity at all levels, including genetic, becomes increasingly important. Except for tropical forests and true deserts, African wildcats occur across the African continent; however, almost no work has been carried out to assess its genetic status and extent of hybridization with domestic cats. For example, in South Africa it has been argued that the long‐term viability of maintaining pure wildcat populations lies in large protected areas only, isolated from human populations. Two of the largest protected areas in Africa, the Kgalagadi Transfrontier and Kruger National Parks, as well as the size of South Africa and range of landscape uses, provide a model situation to assess how habitat fragmentation and heterogeneity influences the genetic purity of African wildcats. Using population genetic and home range data, we examined the genetic purity of African wildcats and their suspected hybrids across South Africa, including areas within and outside of protected areas. Overall, we found African wildcat populations to be genetically relatively pure, but instances of hybridization and a significant relationship between the genetic distinctiveness (purity) of wildcats and human population pressure were evident. The genetically purest African wildcats were found in the Kgalagadi Transfrontier Park, while samples from around Kruger National Park showed cause for concern, especially combined with the substantial human population density along the park's boundary. While African wildcat populations in South Africa generally appear to be genetically pure, with low levels of hybridization, our genetic data do suggest that protected areas may play an important role in maintaining genetic purity by reducing the likelihood of contact with domestic cats. We suggest that approaches such as corridors between protected areas are unlikely to remain effective for wildcat conservation, as the proximity to human settlements around these areas is projected to increase the wild/domestic animal interface. Thus, large, isolated protected areas will become increasingly important for wildcat conservation and efforts need to be made to prevent introduction of domestic cats into these areas.     

Secondary poisoning of stoats (Mustela erminea), feral ferrets (Mustela furo), and feral house cats (Felis catus) by the anticoagulant poison,brodifacoum

Abstract

The extent of darkening of melanin‐based plumages in birds has previously been linked with increasing aggressive encounters between individuals. The North Island robin (Petroica longipes) is a territorial New Zealand endemic passerine that displays delayed plumage maturation (darkening of the plumage with age). Aggressive boundary interactions in the robin are relatively common during the breeding season, when territories are protected and juveniles are dispersing. This study tests the hypothesis of aggression‐mediated plumage darkening in a population of North Island robins by examining if males and older (darker) birds are either (1) involved in a higher number of aggressive interactions, or (2) are more often the aggressor than females and younger birds. When sex and age are accounted for, darker individuals will be either (3) involved in a higher number of interactions or (4) more often the aggressor in encounters with other individuals. Data were collected by scoring the plumage darkness of 32 individuals in the field, and observing (1) interaction behaviours, and (2) age and sex of the birds involved in each interaction. The results show no support for any aggression‐mediated plumage darkness in the robin; males and older birds were not involved in more aggressive interactions, and were not more often the aggressor; and neither the frequency of interactions or the number of aggressive interactions were correlated with a darker plumage. Other more complex mechanisms may explain delayed plumage darkness in the North Island robin.