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Vole Density (vole + density)
Selected AbstractsThe role of food supply in the dispersal behaviour of juvenile Tawny Owls Strix alucoIBIS, Issue 2 2003C. F. Coles We investigated the effects of food supply on decisions made by dispersing juvenile Tawny Owls Strix aluco in Kielder Forest, Northumberland, in 1996 and 1997. Field Voles Microtus agrestis were the main food of the owls and clear-cuts the main habitat for voles. A vole sign index was used to estimate vole abundance. In areas near to roosting owls, mean vole densities were 83 and 115 ha,1 in 1996 and 1997, respectively. The prediction that birds would perform area-restricted searches when prey was more abundant was not confirmed. Moreover, we found no evidence that juveniles avoided conspecifics. Owls appeared to have an imperfect knowledge of the environment as they responded to variability in Field Vole densities by altering the time spent in different areas rather than by moving to areas with successively greater vole densities. Vole abundance explained 25.7% of the variation in the time spent in different areas. Movements did not decrease with time after dispersal, although the detection of such movements was prone to error. This study supports recent work suggesting that although dispersal may be initiated by a variety of proximate and ultimate factors, individual decisions made during dispersal may depend partly on environmental conditions encountered during the process itself. [source] Pulsed resources affect the timing of first breeding and lifetime reproductive success of tawny owlsJOURNAL OF ANIMAL ECOLOGY, Issue 2 2010A. Millon Summary 1.,According to life-history theory, environmental variability and costs of reproduction account for the prevalence of delayed reproduction in many taxa. Empirical estimates of the fitness consequences of different ages at first breeding in a variable environment are few however such that the contributions of environmental and individual variability remains poorly known. 2.,Our objectives were to elucidate processes that underpin variation in delayed reproduction and to assess lifetime consequences of the age of first breeding in a site-faithful predator, the tawny owl Strix aluco L. subjected to fluctuating selection linked to cyclical variation in vole density (typically 3-year cycles with low, increasing and decreasing vole densities in successive years). 3.,A multistate capture,recapture model revealed that owl cohorts had strikingly different juvenile survival prospects, with estimates ranging from 0·08 to 0·33 respectively for birds born in Decrease and Increase phases of the vole cycle. This resulted in a highly skewed population structure with >75% of local recruits being reared during Increase years. In contrast, adult survival remained constant throughout a vole cycle. The probability of commencing reproduction was lower at age 1 than at older ages, and especially so for females. From age 2 onwards, pre-breeders had high probabilities of entering the breeding population. 4.,Variation in lifetime reproductive success was driven by the phase of the vole cycle in which female owls started their breeding career (26,47% of variance explained, whether based on the number of local recruits or fledglings), more than by age at first breeding or by conditions experienced at birth. Females who postponed reproduction to breed for the first time at age 3 during an Increase phase, produced more recruits, even when accounting for birds that may have died before reproduction. No such effects were detected for males. 5.,Sex-specific costs of early reproduction may have accounted for females being more prone to delay reproduction. Contrary to expectations from a best-of-a-bad job strategy, early-hatched, hence potentially higher-quality females were more likely to breed at age 1, but then experienced rapidly declining food resources and so seemed caught in a life-history trap set by the multiannual vole cycle. [source] Phase dependence in winter physiological condition of cyclic volesOIKOS, Issue 4 2007Otso Huitu Lack of food resources has been suggested as a factor which limits the growth of cyclic vole populations. During peak phases of the cycle, vole population growth typically ceases during late autumn or early winter, and is followed by a decrease in density over the winter. To investigate whether this decrease is due to increased mortality induced by a depletion of food resources, we studied overwinter food consumption and physiological condition of field voles (Microtus agrestis) in western Finland in both an increase and a decrease phase of a three-year population cycle. The growth rate of vole populations was negatively related both to prevailing vole densities and to densities six months earlier. The condition index of voles, as well as their blood levels of haematocrit, proteins, free fatty acids and immunoglobulin G, were positively related to population growth rate when populations were declining. When populations were increasing, these parameters tended to be negatively related to population growth rate. The overall physiological condition of voles was lower in the winter of the decrease phase as compared to the increase phase. The return rate of voles, a proxy of survival, was also lower in the decrease than in the increase phase of the cycle and positively related to haematocrit levels. Almost 90% of all green vegetation shoots were consumed by voles during the winter of the decrease phase while only two thirds were eaten in the increase phase. Our results suggest that the winter decrease phase of cyclic vole populations is associated with both a deterioration in the physiological condition of voles and a significant depletion of winter food resources. This implies that malnutrition induces poor physiological condition in voles, which in turn may increase mortality either directly through starvation or indirectly through increased susceptibility to predators and pathogens. [source] Pulsed resources affect the timing of first breeding and lifetime reproductive success of tawny owlsJOURNAL OF ANIMAL ECOLOGY, Issue 2 2010A. Millon Summary 1.,According to life-history theory, environmental variability and costs of reproduction account for the prevalence of delayed reproduction in many taxa. Empirical estimates of the fitness consequences of different ages at first breeding in a variable environment are few however such that the contributions of environmental and individual variability remains poorly known. 2.,Our objectives were to elucidate processes that underpin variation in delayed reproduction and to assess lifetime consequences of the age of first breeding in a site-faithful predator, the tawny owl Strix aluco L. subjected to fluctuating selection linked to cyclical variation in vole density (typically 3-year cycles with low, increasing and decreasing vole densities in successive years). 3.,A multistate capture,recapture model revealed that owl cohorts had strikingly different juvenile survival prospects, with estimates ranging from 0·08 to 0·33 respectively for birds born in Decrease and Increase phases of the vole cycle. This resulted in a highly skewed population structure with >75% of local recruits being reared during Increase years. In contrast, adult survival remained constant throughout a vole cycle. The probability of commencing reproduction was lower at age 1 than at older ages, and especially so for females. From age 2 onwards, pre-breeders had high probabilities of entering the breeding population. 4.,Variation in lifetime reproductive success was driven by the phase of the vole cycle in which female owls started their breeding career (26,47% of variance explained, whether based on the number of local recruits or fledglings), more than by age at first breeding or by conditions experienced at birth. Females who postponed reproduction to breed for the first time at age 3 during an Increase phase, produced more recruits, even when accounting for birds that may have died before reproduction. No such effects were detected for males. 5.,Sex-specific costs of early reproduction may have accounted for females being more prone to delay reproduction. Contrary to expectations from a best-of-a-bad job strategy, early-hatched, hence potentially higher-quality females were more likely to breed at age 1, but then experienced rapidly declining food resources and so seemed caught in a life-history trap set by the multiannual vole cycle. [source] Spatial synchrony in field vole Microtus agrestis abundance in a coniferous forest in northern England: the role of vole-eating raptorsJOURNAL OF APPLIED ECOLOGY, Issue 2000S.J. Petty 1.,The regional synchrony hypothesis (RSH) states that synchrony in microtine abundance over large geographical areas is caused by nomadic avian predators that specialize on small mammals for food. This has proved a difficult hypothesis to test because experiments at an appropriate scale are almost impossible. 2.,We used the decline of the most abundant, nomadic vole-eating raptors in an extensive conifer forest in northern England (Kielder Forest) as a natural experiment to evaluate their influence on synchronizing voles at different spatial scales. Field vole populations fluctuated on a 3,4-year cycle of abundance, similar to the periodicity in central Fennoscandia. 3.,Over a 23-year period, the combined numbers and density of kestrels and short-eared owls significantly declined. If these raptors were responsible for synchronizing vole abundance, the decline should have been associated with a decrease in synchrony. We could find no change in synchrony during the period of the greatest decline in kestrel and short-eared owl numbers (1980,97). 4.,In Kielder, vole abundance has been shown to change in a wave-like manner, with synchrony in the direction of the wave being 5,10-fold smaller than that reported in Fennoscandia. Tawny owls are sedentary and the most abundant vole-eating raptor in our study area, and might have an equalizing influence on vole abundance over smaller areas if they foraged in a density-dependent manner and responded functionally to increasing vole density. If this was the case, spatial variability in vole density should have been less in occupied than unoccupied owl territories, especially in years of low vole density when owls could take a larger proportion of the standing crop of voles. Even though tawny owls caught a significant proportion of the vole population, we could find no difference in variation in vole density between owl territories that were unoccupied, occupied with no breeding attempt, or occupied with a successful breeding attempt. 5.,We conclude that the small-scale synchrony in field vole abundance is unlikely to be caused by avian predators. Instead, it is more likely to be related to the pattern of clear-cutting that has developed in Kielder, which restricts vole dispersal. If this assumption is correct, we would predict more widespread synchrony in vole abundance in first-generation forests when extensive areas are planted over short periods of time, and this is supported by anecdotal evidence. These conclusions indicate that foresters may be able to manipulate the spatial dynamics of voles and vole predators by varying patch sizes within forests. [source] Disturbance and habitat use: is edge more important than area?OIKOS, Issue 1 2006Alissa E. Moenting In their efforts to maximize fitness while reducing the probability of dying, animals must decide which patches to forage in, when to forage, and how long to forage in each patch. Each decision will be modified by habitat and habitat disturbance. We evaluate the effects of habitat disturbance on foraging behaviour by imagining an initially homogeneous environment that is altered to create patches of different sizes. Disturbance increases predation risk, or otherwise alters patch profitability. Foragers can respond by changing their pattern of foraging, or by reducing their activity. We develop predictions for each scenario. We then test the predictions with data on the abundance and foraging activity of meadow voles (Microtus pennsylvanicus) in and around four sizes of circular disturbed patches. We created the patches by mowing vegetation in an abandoned hay field in northern Ontario, Canada. The treatments had no effect on vole density, and there was no consistent relationship between vole activity and distance from the edge of disturbed patches. Incidental predation of sunflower seeds, our measure of vole foraging behaviour, declined linearly with increasing patch circumference (edge). Seed consumption by meadow voles, and predation by voles on lower food levels, correlates with the length of edge habitat rather than with the area disturbed. Adaptive behaviour can thereby explain edge effects that, under current priorities emphasizing area, would appear at odds with conservation ecology. [source] Cyclic voles, prey switching in red fox, and roe deer dynamics , a test of the alternative prey hypothesisOIKOS, Issue 2 2003Petter Kjellander Medium-sized predators sometimes switch to alternative prey species as their main prey declines. Our objective of this study was to test the alternative prey hypothesis for a medium sized predator (red fox, Vulpes vulpes), a small cyclically fluctuating main prey (microtine voles) and larger alternative prey (roe deer fawns, Capreolus capreolus). We used long-term time series (28 years) on voles, red fox and roe deer from the Grimsö Wildlife Research Area (59°40,N, 15°25,E) in south-central Sweden to investigate interspecific relationships in the annual fluctuations in numbers of the studied species. Annual variation in number of roe deer fawns in autumn was significantly and positively related to vole density and significantly and negatively related to the number of fox litters in the previous year. In years of high vole density, predation on roe deer fawns was small, but in years of low vole density predation was more severe. The time lag between number of fox litters and predation on fawns was due to the time lag in functional response of red fox in relation to voles. This study demonstrates for the first time that the alternative prey hypothesis is applicable to the system red fox, voles and roe deer fawns. [source] | ||||||||||