Although females are the choosier sex in most species, male mate choice is expected to occur under certain conditions. Theoretically, males should prefer larger females as mates in species where female fecundity increases with body size. However, any fecundity‐related benefits accruing to a male that has mated with a large female may be offset by an associated fitness cost of shared paternity if large females are more likely to be multiply mated than smaller females in nature. We tested the above hypothesis and assumption using the Trinidadian guppy (Poecilia reticulata) by behaviourally testing for male mate choice in the laboratory and by ascertaining (with the use of microsatellite DNA genotyping) patterns of male paternity in wild‐caught females. We observed significant positive relationships between female body length and fecundity (brood size) and between body length and level of multiple paternity in the broods of females collected in the Quaré River, Trinidad. In laboratory tests, a preference for the larger of two simultaneously‐presented virgin females was clearly expressed only when males were exposed to the full range of natural stimuli from the females, but not when they were limited to visual stimuli alone. However, as suggested by our multiple paternity data, males that choose to mate with large females may incur a larger potential cost of sperm competition and shared paternity compared with males that mate with smaller females on average. Our results thus suggest that male guppies originating from the Quaré River possess mating preferences for relatively large females, but that such preferences are expressed only when males can accurately assess the mating status of encountered females that differ in body size.
Estimating animal abundance and density are fundamental goals of many wildlife monitoring programs. Camera trapping has become an increasingly popular tool to achieve these monitoring goals due to recent advances in modeling approaches and the capacity to simultaneously collect data on multiple species. However, estimating the density of unmarked populations continues to be problematic due to the difficulty in implementing complex modeling approaches, low precision of estimates, and absence of rigor in testing of model assumptions and their influence on results. Here, we describe a novel approach that uses still image camera traps to estimate animal density without the need for individual identification, based on the time spent in front of the camera (TIFC). Using results from a large-scale multispecies monitoring program with nearly 3000 cameras deployed over 6 years in Alberta, Canada, we provide a reproducible methodology to estimate parameters and we test key assumptions of the TIFC model. We compare moose (Alces alces) density estimates from aerial surveys and TIFC, including incorporating correction factors for known TIFC assumption violations. The resulting corrected TIFC density estimates are comparable to aerial density estimates. We discuss the limitations of the TIFC method and areas needing further investigation, including the need for long-term monitoring of assumption violations and the number of cameras necessary to provide precise estimates. Despite the challenges of assumption violations and high measurement error, cameras and the TIFC method can provide useful alternative or complementary animal density estimates for multispecies monitoring when compared to traditional monitoring methods.
We examined 11 years of data on reproductive success, survival, and population dynamics of two populations (Fortress and Grizzly) of deer mice (Peromyscus maniculatus) in the Kananaskis Valley, Alberta, to investigate the extent to which the dynamics of these populations is dictated by weather conditions. Summer population growth was not related to the population growth in the winter preceding the breeding season or to spring population density. Over the summer on the Fortress grid, population growth was positively related to adult survival, whereas on the Grizzly grid, population growth was positively related to nestling survival. Neither summer population growth nor demographic correlates of summer population growth was consistently related to weather patterns. On Fortress, adult survival during the breeding season was negatively correlated with precipitation. On Grizzly, nestling survival during the breeding season was negatively correlated with precipitation. Winter population growth was inversely proportional to the fall population density prior to the winter but neither was related to weather conditions. Climate limits seasonal breeding in these populations, but compensatory responses appear sufficient to accommodate extreme weather conditions during both the breeding and nonbreeding seasons.
Deer mice (Peromyscus maniculatus (Wagner, 1845)) in the Kananaskis Valley were monitored from 1985 to 2003 by livetrapping, and first parturition dates were compared among years and examined in relation to spring weather. On average, first litters were conceived on 2 May, well after the winter snowpack melted (19 March) and just before average temperatures reached 0 °C (8 May). First parturitions took place on 26 May, when average temperatures were above freezing. The average temperature at the time of conceptions (late April – early May) declined by approximately 2 °C, and the date that the average temperatures reached 0 °C was 11 days later, between 1985 and 2003, with potential effects for summer phenology. Spring temperatures, but not snowfall, were related to the El Niño Southern Oscillation index. The initiation of breeding by deer mice was variable among years, but was not related to snowfall or temperature and did not change, on average, between 1985 and 2003. The decrease in spring temperatures had no noticeable effects on breeding success. We conclude that photoperiod may be a primary cue for the initiation of spring breeding and that food resources over winter may explain the among-year variation in the initiation of breeding.
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