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Natal Dispersal Distances (natal + dispersal_distance)
Selected AbstractsConsequences of dispersal for the quantitative study of adaptation in small-scale plots: a case study of an avian island populationECOGRAPHY, Issue 5 2000M. M. Lambrechts Lifetime recruitment of breeding offspring estimated in small-scale study plots (i.e. local recruitment) is considered to be the best available ecological measure of contributions to following generations, and sufficient for the quantitative study of adaptation in natural populations. Recent investigations suggest that local recruitment of breeding offspring does not always reflect the total recruitment in the whole population, especially in small-scale plots where the majority of locally-born offspring leave these plots to breed elsewhere. We examined in an avian island population whether study plot size has an important impact on different population and fitness measures. We defined around a central nestbox seven plots, varying in radius from 100 to 700 m. We show that in the smallest plots, the local replacement rate of adults by breeding offspring is low, the number of locally-born offspring settling beyond the limits of a plot is high, and relationships between local and total recruitment are weak. This is especially true for daughters as more daughters than sons settle beyond the limits of local plots for breeding. Our interpretation is that the lifetime recruitment of breeding offspring in local plots does not necessarily reflect the lifetime recruitment of breeding offspring in the whole population, especially when plots do not cover the natal dispersal distance. Consequences of dispersal for the quantitative study of adaptation are discussed. [source] Female-biased natal and breeding dispersal in an alpine lizard, Niveoscincus microlepidotusBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 2 2003MATS OLSSON We measured two aspects of dispersal in the alpine Australian scincid lizard, Niveoscincus micolepidotus: (1) natal dispersal, i.e. shift in home range over the lizard's first year of life, and (2) breeding dispersal, i.e. shifts of home ranges between breeding attempts as adults. On average, displacements were surprisingly small. Female neonates dispersed about twice as far as did males in the same cohort (means of 12 m vs. 6 m). A female's natal dispersal distance was not correlated with her body size or our estimate of physiological performance (sprint speed). However, larger, faster-running male neonates dispersed further than did smaller, slower males. As was the case for neonates, adult females moved significantly further between breeding seasons than did adult males (14.2 m vs. 9.6 m). Because of a female's long gestation period (more than 1 year), two groups of females occur simultaneously in the population, non-ovulated (i.e. with yolking folicles) and pregnant females (i.e. approaching parturition). Females that were not yet ovulated showed a markedly stronger dispersal in response to high reproductive effort (i.e. clutch size in relation to body condition) than did pregnant females. In adult males, body size was negatively correlated with dispersal distance, suggesting that although males have overlapping territories, they exhibit an increasing level of site tenacity with age and/or size. Thus, selection for the relatively more pronounced site tenacity in adult males may have resulted in the more marked philopatric behaviour compared to females also as neonates. © 2003 The Linnean Society of London, Biological Journal of the Linnean Society, 2003, 79, 277,283. [source] Estimating natal dispersal movement rates of female European ducks with multistate modellingJOURNAL OF ANIMAL ECOLOGY, Issue 6 2003Peter Blums Summary 1We used up to 34 years of capture,recapture data from about 22 100 new releases of day-old female ducklings and multistate modelling to test predictions about the influence of environmental, habitat and management factors on natal dispersal probability of three species of ducks within the Engure Marsh, Latvia. 2The mean natal dispersal distances were very similar (c. 0·6,0·7 km) for all three species and were on average 2·7 times greater than breeding dispersal distances recorded within the same study system. 3We were unable to confirm the kinship hypothesis and found no evidence that young first-nesting females nested closer to their relatives (either mother or sister) than to the natal nest. 4Young female northern shovelers, like adults, moved from small islands to the large island when water level was high and vice versa when water level was low before the construction of elevated small islands. Movement probabilities between the two strata were much higher for young shovelers than adults, suggesting that young birds had not yet developed strong fidelity to the natal site. Movements of young female tufted ducks, unlike those of shovelers, were not dependent on water level fluctuations and reflected substantial flexibility in choice of first nesting sites. 5Data for young birds supported our earlier conclusion that common pochard nesting habitats in black-headed gull colonies were saturated during the entire study period. Young females, like the two adult age groups, moved into and out of colonies with similar probability. Fidelity probability of female pochards to each stratum increased with age, being the lowest (0·62) for young (DK) females, intermediate (0·78) for yearlings (SY) and the highest (0·84) for adult (ASY) females. 6Young female tufted ducks, like adults, showed higher probabilities of moving from islands to emergent marshes when water levels were higher both before and after habitat management. The relationship between the spring water levels and movement was much weaker for young females than for adults. 7Young female diving ducks exhibited much stronger (compared to adults) asymmetric movement with respect to proximity to water, with higher movement probabilities to near-water locations than away from these locations. 8Local survival of day-old ducklings during the first year of life was time-specific and very low (means for different strata/states 0·01,0·08) because of high rates of emigration and prefledging mortality. [source] Limited dispersal by Nazca boobies Sula grantiJOURNAL OF AVIAN BIOLOGY, Issue 1 2004Kathryn P. Huyvaert We documented natal and breeding dispersal at several spatial scales by Galápagos Nazca boobies Sula granti, a wide-ranging pelagic seabird. We found exceptionally low degrees of both types of dispersal despite these birds' vagility. Median natal dispersal distances were 26 m and 105 m for males and females, respectively. Median breeding dispersal distances for both sexes were 0 m. No natal or breeding dispersals occurred from our study site at Punta Cevallos, Isla Española to six other colonies in the Galápagos, but we did document four long-distance natal dispersals from Punta Cevallos to islands near the South American coast. Recaptures and dead recoveries of ringed birds showed long distance non-breeding movements to the Central American coast and elsewhere in the eastern Pacific, contrasting with the very limited dispersal to breeding sites. [source] Natal dispersal of European hare in FranceJOURNAL OF ZOOLOGY, Issue 4 2007Y. Bray Abstract Dispersal is a fundamental process with wide-ranging evolutionary and management consequences. To date, natal dispersal has never been described for the polygynous-promiscuous European hare Lepus europaeus. Using telemetry, we investigated the natal dispersal pattern in two zones that differed in hunting pressure and hare density. We quantified both the natal dispersal rates and distances using 84 juvenile hares. We tested for the influence of several factors (age, sex, density and period of the year) on these two variables. Overall, the mean dispersal rate was 43% and the median natal dispersal distances were 209 m for philopatric hares and 1615 m for dispersers. The maximum distance moved was 17.35 km. Natal dispersal rates were higher in the hunting zone with less density for both males and females, but males dispersed more frequently than females in the two zones although females moved over longer distances. Natal dispersal occurred preferentially between 4 and 6 months of age. This very fine description of the natal dispersal pattern allowed us to make inferences about both the evolutionary and proximate causes of natal dispersal. We also advocate that more attention should be paid to dispersal in studies on hare dynamics and on the conception of hare management, because dispersal seems to be more common than previously thought. [source] | ||||||||||