The effect of habitat on the breeding season survival of Mallards (Anas platyrhynchos) in the Great Lakes region

2018 ◽  
Vol 96 (7) ◽  
pp. 700-706
Author(s):  
Ryan A. Boyer ◽  
John M. Coluccy ◽  
Robert A. Montgomery ◽  
Kyle M. Redilla ◽  
Scott R. Winterstein

Modeling the effect of habitat on animal survival is critical for understanding population dynamics and developing effective habitat management strategies. Despite the importance of this information, knowledge of survival–habitat associations are often lacking, particularly for waterfowl species. Here we evaluated female Mallard (Anas platyrhynchos Linnaeus, 1758) survival during the breeding season in relation to habitat conditions within each individual’s home range. We implanted telemetry transmitters and tracked 283 female Mallards across nine study sites in the Great Lakes region. For each Mallard, we quantified core breeding season home ranges via the creation of utilization distributions (UDs). We then fit known-fate models in the program MARK to predict breeding season survival as a function of the proximity of core home ranges to various habitat types, the proportion of habitat types within the core areas, number of core areas, and home range size. We found that breeding season survival decreased as the proportion of forestland habitat within core home ranges increased (β = −1.740, SE = 0.787). No additional upland or wetland habitat types significantly affected breeding season survival. Managers striving to increase breeding season survival for Mallards should focus their efforts on restoring habitats in areas with low proportions of forestland habitat to mitigate the risk of predation.

2002 ◽  
Vol 8 (4) ◽  
pp. 271 ◽  
Author(s):  
Peter G. Cale

White-browed Babbler Pomatostomus superciliosus groups occupying linear strips of vegetation had breeding territories that were smaller in area and had longer linear dimensions than those occupying patches. A group's non-breeding home range was larger than its breeding territory. Groups occupying linear/patch home ranges expanded the linear extent and area of their home ranges more than those within other home range configurations. Some groups moved during the non-breeding season and this was more likely to occur if the group occupied a remnant with a low abundance of invertebrates during summer. Some groups that moved returned prior to the next breeding season, but the majority were never seen again. New groups moved into the study sites and established in vacant home ranges. This suggests that those groups that left the study sites may have established new home ranges elsewhere. Breeding site fidelity was lower in groups that had failed in previous breeding attempts. Therefore, group movements were influenced by the feeding and breeding quality of the habitat. However, the configuration of the local population also influenced group movements with those groups on the edge of a local population being more likely to move than those in the interior. New groups were formed by two processes; group dispersal, where groups generally filled a vacant home range, and group budding, which involved the splitting of a large group. Group dispersal maintained group densities while group budding increased the density of groups in a local population. These two processes were common, producing localized fluctuations in the density of groups. Since babbler groups contain only one breeding pair, changes in group density represent changes in effective population size. Therefore, group dynamics may be important to the persistence of local populations of White-browed Babblers, especially in landscapes that have suffered from habitat loss and fragmentation.


1994 ◽  
Vol 21 (1) ◽  
pp. 65 ◽  
Author(s):  
A Horsup

The home range and movements of the allied rock wallaby, Petrogale assimilis, a small macropod of the seasonally wet-dry tropics of Queensland, were studied over a 22-month period. There was no significant difference in the size of home ranges (95% isopleth) or core areas (65% isopleth) of males and females. Home ranges were generally elliptical with a mean size of 11.9 ha. Season had a major effect on home ranges. The following measures were all significantly greater in the dry seasons than in the wet seasons: home-range size (larger), home-range shape (more elongate), distance moved by females when feeding (longer), distance between shelter site and home-range centre of activity (longer). Feeding movements of males did not vary seasonally and were as long as dry-season movements of females, suggesting that movements of males are primarily determined by behavioural rather than physiological considerations. The overlap of rock-wallaby home ranges varied little between the sexes or seasons and averaged 38%. Core areas overlapped by an average of 22%; however, feeding adult rock-wallabies rarely met other conspecifics, except their partners. A comparison of the fixes of unpaired wallabies that had overlapping home ranges showed that temporal separation was occurring. In contrast, the home ranges of consort pairs showed extremely high temporal and spatial overlap. Rock-wallabies exhibited strong fidelity to their home ranges. The overlap of the seasonal home ranges and core areas of each individual rock wallaby averaged 68% and 52%, respectively. However, the seasonal home range of a socially immature adult male altered in location and size as he matured socially until it stabilised when he obtained a permanent consort.


2016 ◽  
Vol 38 (2) ◽  
pp. 158 ◽  
Author(s):  
Stephen Phillips

The effects of short-term disturbances that result in changes to movement patterns and/or behaviour of wildlife are poorly understood. In this study the movements of seven koalas were monitored before, during and after a five-day music festival. During the monitoring program koalas occupied home-range areas of 0.6–13 ha with one or more core areas of activity. Aversive behaviour in the form of evacuation of known ranging areas was demonstrated by three koalas that had core areas within 525 m of the approximate centre of the festival area, the associated responses comprising movements that were perpendicular to and away from staging areas where music was played. Responses contained within known ranging areas were observed in three other koalas whose core areas were located up to 600 m away. The type of response appeared related to the proximity of koala home ranges to music-staging areas, while the maximum distance associated with an aversive response was 725 m. Six of the radio-tracked koalas returned to their home-range areas following the conclusion of festival activities. While the specific stimulus eliciting aversive behaviour was not identified, responses in all instances were initiated during the musical phase of the festival event. The potential for short-term disturbances such as music festivals to significantly influence the ranging patterns of koalas warrants recognition of possible longer-term ecological consequences for planning and management purposes.


1998 ◽  
Vol 76 (3) ◽  
pp. 592-596 ◽  
Author(s):  
Anne H Hubbs ◽  
Rudy Boonstra

We used radiotelemetry to study the effects of food addition and predator reduction on the home-range sizes of adult Arctic ground squirrels (Spermophilus parryii) on large-scale experimental grids in the boreal forest of the southwestern Yukon Territory. Home ranges were 2-7 times smaller on food-supplemented grids than on nonsupplemented grids, regardless of whether large mammalian predators were present. Similarly, core areas (where 50% of activities occur) were 8-11 times smaller on food-supplemented grids. Food availability rather than predator presence primarily determined the sizes of home ranges and core areas of Arctic ground squirrels.


2006 ◽  
Vol 84 (4) ◽  
pp. 573-582 ◽  
Author(s):  
J.K. Young ◽  
W.F. Andelt ◽  
P.A. Terletzky ◽  
J.A. Shivik

Most ecological studies of coyotes are of short duration and studies are generally never repeated, thus the opportunity to compare changes in coyote ( Canis latrans Say, 1823) ecology over time is rare. We compared coyote home ranges, activity patterns, age, and diet at the Welder Wildlife Refuge in south Texas between 1978–1979 and 2003–2004 (25 years later). The Minta index of overlap between 1978 and 2003 home ranges was 51.7 ± 7.0 (n = 7), much greater than the Minta index value based on randomized tests (28.7 ± 8.6), indicating similar spatial patterns between time periods. The Minta index was 12.3 ± 6.2 (n = 7) for core areas, whereas the Minta index value based on randomized tests was 4.0 ± 3.0. Although overall diets were similar between 1978 and 2003, we detected some differences in prey species consumed. Activity patterns were similar between the two study periods, with peaks in movement occurring around sunrise and sunset. There was no difference in the mean age between the two populations (P = 0.44, n = 68, t[66] = 2.00). Our findings suggest that population features, such as home-range position and age structure, are similar between extended time periods, while individual-level patterns, such as the prey species consumed and distribution of locations within a home range, are dynamic and may reflect changes in the local environment.


2005 ◽  
Vol 32 (7) ◽  
pp. 587 ◽  
Author(s):  
Robyn Molsher ◽  
Chris Dickman ◽  
Alan Newsome ◽  
Warren Müller

Twenty-one feral cats were radio-tracked using direct sighting and triangulation techniques (amassing 730 location fixes) during winter in an agricultural landscape in central-western New South Wales. Factors affecting home-range size, home-range overlap and habitat use were assessed. Mean home-range size was 248 ha (s.e. = 34.9, n = 15 cats, 598 location fixes). Home-range size and habitat use were not influenced by sex or age of adult cats, prey abundance or time of day. However, cat weight significantly influenced range size, with heavier cats having larger ranges than smaller cats. Although the cats are apparently solitary, their home ranges overlapped considerably, particularly between young adults and old adult cats. Cats were active both by day and night and did not occupy permanent dens. Home ranges encompassed mixed habitat types that provided both shelter and prey. Open woodland and open forest were the main habitat types covered by home ranges, but within these areas cats showed a preference for grassland, where rabbits were more abundant. The results recorded in this study indicate that cat-control programs should concentrate in mixed habitat areas, where both shelter and food are available, and over widely dispersed areas. The absence of group living suggests that the effectiveness of virally vectored fertility or biological control agents would be limited.


2004 ◽  
Vol 31 (3) ◽  
pp. 327 ◽  
Author(s):  
Helen Puckey ◽  
Milton Lewis ◽  
David Hooper ◽  
Carrie Michell

Radio-telemetry was used to examine the home range, movement and habitat utilisation of the critically endangered Carpentarian rock-rat (Zyzomys palatalis) in an isolated habitat patch in the Gulf of Carpentaria hinterland over a 13-month period. Two home-range estimators were used in the study, (i) minimum convex polygon (MCP) and (ii) fixed Kernel (KL), the latter also being used to estimate core areas of activity. Based on a total sample size of 21 individuals, the mean MCP home range was 11 165 m2, similar to the mean KL home range of 10 687 m2. Core areas were, on average, 11.9% of the KL home-range estimate. There was no significant difference in the size of home range or core area of males and females. Juveniles had a significantly smaller home range than adults. Home ranges and, to a lesser degree, core areas were non-exclusive, with multiple areas of overlap (averaging 41% and 38% respectively) within and between all age and gender categories, but especially between males and between juveniles. Movement frequencies showed that animals made many short forays in a central area close to the arithmetic home-range mean and far fewer long forays of distances greater than 100 m from the central area. The spatial and temporal activity of Z. palatalis was concentrated in, but not confined to, the 'valley' and 'slope' habitats, with fewer movements of rats onto the surrounding 'plateau'. Resource selection analyses showed that Z. palatalis tended to prefer valley and slope habitats over the plateau and that the proportion of point locations was significantly higher for adults in the slope habitat and for juveniles in the valley habitat. Most home ranges were centred on the ecotone between these two habitat types. Although isolated and spatially limited, these habitat patches provide high-quality resources for dense populations of Z. palatalis. This study exemplifies a species' attempt to make efficient use of a limited resource in an otherwise hostile environment. Even small declines in habitat area or quality due to their vulnerability to fire would impact upon many animals.


Author(s):  
Katherine Gura ◽  
Bryan Bedrosian ◽  
Anna D. Chalfoun ◽  
Susan Patla

Identifying resource requirements of under-studied species during key stages such as breeding is critical for effective management. We quantified breeding-season home-range attributes and habitat selection of adult Great Gray Owls across multiple spatial (home-range and within-home-range level) and temporal (nesting and post-fledging; day versus night) scales in western Wyoming, USA. In 2018 and 2019 we outfitted adult male owls (n = 18) with GPS remote-download transmitters and collected hourly location data throughout the breeding season (1 May – 15 September). Using 50% and 95% kernel density estimates (KDE), mean core area was 1.2 km2 and mean home-range size was 6.2 km2 (n = 16). Resource selection analyses incorporated both remotely-sensed and microsite data. We conducted microsite surveys at used and available points within 95% KDE home ranges using a stratified random sample design (n = 661). Determining home-range and breeding habitat requirements will improve density estimates and facilitate the effective management of Great Gray Owls and their habitat. We found differing patterns between habitat selection at the home-range and within-home-range scales.   Featured photo by YNP on Flickr. https://flic.kr/p/SA17KT


Mammalia ◽  
2018 ◽  
Vol 82 (6) ◽  
pp. 540-549 ◽  
Author(s):  
Roy T. McBride ◽  
Jeffrey J. Thompson

AbstractHome range and core area size were estimated for jaguar (Panthera onca) in western Paraguay in the Dry Chaco, Humid Chaco and Pantanal using an autocorrelated kernel density estimator. Mean home range size was 818 km2(95% confidence interval: 425–1981) in the Dry Chaco and 237 km2(95% confidence interval: 90–427) in the Humid Chaco/Pantanal. Core areas, defined as the home range area where use was equal to expected use, was consistent across sexes and systems represented on average by the 59% home range isopleth (range: 56–64%). Males had a higher probability of larger home ranges and more directional and greater daily movements than females collectively and within systems. The large home ranges in the Dry Chaco are attributable to the relatively low productivity of that semi-arid ecosystem and high heterogeneity in resource distribution while larger than expected home ranges in the Humid Chaco/Pantanal compared to home range estimates from the Brazilian Pantanal may be due to differences in geomorphology and hydrological cycle. The large home ranges of jaguars in western Paraguay and a low proportional area of protected areas in the region demonstrate the importance of private ranchland for the long-term conservation of the species.


The Condor ◽  
2007 ◽  
Vol 109 (4) ◽  
pp. 750-768 ◽  
Author(s):  
Thomas E. Hamer ◽  
Eric D. Forsman ◽  
Elizabeth M. Glenn

Abstract We compared home range areas and habitat selection of radio-marked Spotted Owls (Strix occidentalis) and Barred Owls (Strix varia) in an area of sympatry in the northern Cascade Range of Washington in 1986–1989. On average, home ranges of Spotted Owls were 3–4 times larger than ranges of Barred Owls, and there was little overlap of home ranges during the breeding season. Ranges of both species tended to expand during winter. Home range size of both species was negatively correlated with the amount of old forest, but the negative slope of the regression was much steeper for Spotted Owls than for Barred Owls. For both species, home ranges of individual owls typically had high overlap among seasons and years, indicating high site fidelity. Barred Owls generally occupied home ranges at lower elevations than Spotted Owls (mean  =  386 ± 27 m vs. 750 ± 68 m). Both species tended to use old forests more than expected, but Spotted Owls tended to use other cover types less than expected, whereas Barred Owls used most other cover types in proportion to their availability. We suggest that Spotted Owls may use larger ranges than Barred Owls because they prey selectively on a few species of nocturnal mammals, whereas Barred Owls forage more evenly across a broad range of prey types, including diurnal and aquatic species. The low overlap of Barred Owl and Spotted Owl home ranges suggests that territorial Barred Owls exclude Spotted Owls from their territories, at least during the breeding season, thus reducing the amount of habitat available to Spotted Owls.


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