Foraging strategies of sympatric lagomorphs: implications for differential success in fragmented landscapes

2000 ◽  
Vol 78 (12) ◽  
pp. 2134-2141 ◽  
Author(s):  
Douglas F Smith ◽  
John A Litvaitis

In recent decades, the distribution of New England cottontails (Sylvilagus transitionalis) has declined substantially in response to forest maturation and fragmentation. Populations of eastern cottontails (Sylvilagus floridanus) have expanded into the range of S. transitionalis, since they are apparently less affected by the consequences of habitat modifications. We suspected that S. floridanus was able to exploit small patches of habitat where S. transitionalis was vulnerable to intense predation and we evaluated this explanation using large enclosures within which we manipulated the quality and distribution of food in relation to escape cover. In trials with low-quality food in cover and high-quality food in open areas, S. transitionalis sacrificed food quality for safety by remaining in close proximity to cover. Sylvilagus floridanus avoided low-quality food in cover and foraged at sites containing high-quality food away from cover. When food was removed from cover, S. transitionalis was reluctant to forage in the open and lost a greater proportion of body mass and succumbed to higher rates of predation than did S. floridanus. We applied these results to patterns of foraging by free-ranging rabbits in a fragmented landscape and estimated that S. transitionalis could successfully exploit only 32% of the available habitat without experiencing elevated rates of predation, whereas S. floridanus could exploit 99% of the habitat. Thus, the consequences of habitat fragmentation (especially higher predation risk) may not be as detrimental to S. floridanus, and this species will likely persist, whereas populations of S. transitionalis will continue to decline.

2019 ◽  
Vol 97 (6) ◽  
pp. 516-523 ◽  
Author(s):  
Amanda E. Cheeseman ◽  
Jonathan B. Cohen ◽  
Sadie J. Ryan ◽  
Christopher M. Whipps

In fragmented habitat, population persistence depends in part on patch quality and patch size relative to home-range size. The imperiled New England cottontail (Sylvilagus transitionalis (Bangs, 1895)) is an obligate user of shrublands in the northeastern United States, a highly fragmented and declining ecosystem. New England cottontail conservation efforts have targeted habitat creation; however, efforts are hindered by a limited knowledge of seasonal space use and its relationship to habitat quality, which could help inform minimum patch-size requirements and implications of competition with non-native eastern cottontails (Sylvilagus floridanus (J.A. Allen, 1890)). To address these uncertainties, we modeled home-range areas for both species as a function of season, patch size, sex, and two indicators of forage and cover availability. Home range was generally inversely correlated with measures of forage and cover resources and the response differed by season and species and did not vary with patch size. Instead, inclusion of matrix habitat within home ranges increased with decreasing patch size, placing individuals within smaller patches at a high risk of mortality. These risks may be mitigated in patches >7 ha and absent in patches >20–25 ha where predicted inclusion of matrix is lower or absent.


2021 ◽  
Author(s):  
Robbie I’Anson Price ◽  
Francisca Segers ◽  
Amelia Berger ◽  
Fabio S Nascimento ◽  
Christoph Grüter

Abstract Social information is widely used in the animal kingdom and can be highly adaptive. In social insects, foragers can use social information to find food, avoid danger or choose a new nest site. Copying others allows individuals to obtain information without having to sample the environment. When foragers communicate information they will often only advertise high quality food sources, thereby filtering out less adaptive information. Stingless bees, a large pantropical group of highly eusocial bees, face intense inter- and intra-specific competition for limited resources, yet display disparate foraging strategies. Within the same environment there are species that communicate the location of food resources to nest-mates and species that do not. Our current understanding of why some species communicate foraging sites while others do not is limited. Studying freely foraging colonies of several co-existing stingless bee species in Brazil, we investigated if recruitment to specific food locations is linked to (1) the sugar content of forage, (2) the duration of foraging trips and (3) the variation in activity of a colony from one day to another and the variation in activity in a species over a day. We found that, contrary to our expectations, species with recruitment communication did not return with higher quality forage than species that do not recruit nestmates. Furthermore, foragers from recruiting species did not have shorter foraging trip durations than those from weakly-recruiting species. Given the intense inter- and intraspecific competition for resources in these environments, it may be that recruiting species favour food resources that can be monopolised by the colony rather than food sources that offer high-quality rewards.


2021 ◽  
Author(s):  
Fen Guo ◽  
Stuart E. Bunn ◽  
Michael T. Brett ◽  
Hannes Hager ◽  
Martin J. Kainz

Behaviour ◽  
2004 ◽  
Vol 141 (2) ◽  
pp. 233-244 ◽  
Author(s):  
Joanne Tuck ◽  
Mark Hassall

AbstractForaging behaviour of Armadillidium vulgare was observed in laboratory arenas in which the spatial distribution of patches of high quality food (powdered dicotyledonous leaf litter) was varied within a background of low quality food (powdered grass leaf litter). The hypotheses that the foraging behaviour and foraging path of A. vulgare would be influenced by food quality and the patchiness of high quality food resources were tested. More time was spent in high quality food patches than in low quality food backgrounds than expected by chance in all heterogeneity treatments, but an increasingly higher percentage of time was spent in low quality food as the high quality food became more clumped in space. More time was spent searching, but less time was spent feeding in low quality food backgrounds than in high quality food patches in all the treatments. Walking speed was found to be lower in high quality food patches than in low quality food backgrounds and this was not affected by treatment. Turning frequency and turning angle were found to be higher in high quality food patches than in low quality backgrounds. Turning frequency in low quality food backgrounds decreased as the high quality food became more clumped in space, whereas turning angle in high quality food patches significantly increased in the patchy, but then decreased again in the clumped treatment. The effects of varying the spatial heterogeneity of high quality foods on the trade-off between costs of searching and intake benefits for saprophages are discussed in relation to predictions from optimal foraging theory for circumstances when intake rate maximisation is affected by the constraint of limited nutrients.


Author(s):  
Vaclav Smil

This chapter discusses the use of energy during prehistoric times. Our direct ancestors spent their lives as simple foragers, and it was only about 10,000 years ago that the first small populations of our species began a sedentary existence based on the domestication of plants and animals. This means that for millions of years, the foraging strategies of hominins resembled those of their primate ancestors, but we now have isotopic evidence from East Africa that by about 3.5 million years ago hominin diets began to diverge from those of extant apes. The chapter first considers how bipedalism started a cascade of enormous evolutionary adjustments such as adaptations underlying tool use and adaptation to high-quality, energy-dense foods (meat, nuts) before providing an overview of foraging societies and the origins of agriculture.


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