11 research outputs found

    Demographic response of snake-necked turtles correlates with indigenous harvest and feral pig predation in tropical northern Australia

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    The definitive version is available at www.blackwell-synergy.com1. Species that mature late, experience high levels of survival and have long generation times are more vulnerable to chronic increases in mortality than species with higher fecundity and more rapid turnover of generations. 2. Many chelonians have low hatchling survival, slow growth, delayed sexual maturity and high subadult and adult survival. This constrains their ability to respond quickly to increases in adult mortality from harvesting or habitat alteration. In contrast, the northern snake-necked turtle Chelodina rugosa (Ogilby 1890) is fast-growing, early maturing and highly fecund relative to other turtles, and may be resilient to increased mortality. 3. Here we provide correlative evidence spanning six study sites and three field seasons, indicating that C. rugosa is able to compensate demographically to conditions of relatively low subadult and adult survival, caused by pig Sus scrofa (Linnaeus 1758) predation and customary harvesting by humans. 4. Recruitment and age specific fecundity tended to be greater in sites with low adult and subadult survival (and thus reduced densities of large turtles), owing to higher juvenile survival, a smaller size at onset of maturity and faster post-maturity growth. 5. These patterns are consistent with compensatory density-dependent responses, and as such challenge the generality that high subadult and adult survival is crucial for achieving long-term population stability in long-lived vertebrates such as chelonians. 6. We posit that long-lived species with ‘fast’ recruitment and a capacity for a compensatory demographic response, similar to C. rugosa, may be able to persist in the face of occasional or sustained adult harvest without inevitably threatening population viability.Damien A. Fordham, Arthur Georges, Barry W. Broo

    Quantification of allochthonous nutrient input into freshwater bodies by herbivorous waterbirds

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    1. Waterbirds are considered to import large quantities of nutrients to freshwater bodies but quantification of these loadings remains problematic. We developed two general models to calculate such allochthonous nutrient inputs considering food intake, foraging behaviour and digestive performance of waterbirds feeding in terrestrial habitats: an intake model (IM), mainly based on an allometric relationship for energy requirements and a dropping model (DM), based on allometric relationships for defaecation.2. Reviewed data of nitrogen (N) and phosphorus (P) content of herbivorous food varied according to diet type (foliage, seeds and roots), season and fertilization. For model parameterization average foliage diet contained 38.20 mg N g&minus;1 and 3.21 mg P g&minus;1 (dry weight), whereas mean faeces composition was 45.02 mg N g&minus;1 and 6.18 mg P g&minus;1.3. Daily allochthonous nutrient input increased with body mass ranging from 0.29 g N and 0.03 g P in teals Anas crecca to 5.69 g N and 0.57 g P in mute swans Cygnus olor. Results from IM differed from those of DM from ducks to swans by 63&ndash;108% for N and by &minus;4 to 23% for P. Model uncertainty was lowest for the IM and mainly caused by variation in estimates of food retention time (RT). In DM food RT and dropping mass determined model uncertainty in similar extent.4. Exemplarily applying the models to Dutch wetlands resulted in mean annual contribution of herbivorous waterbirds to allochthonous nutrient loading of 382.8 &plusmn; 167.1 tonnes N a&minus;1and 34.7 &plusmn; 2.3 tonnes P a&minus;1, respectively, which corresponds to annual surface-water loadings of 1.07 kg N ha&minus;1 and 0.10 kg P ha&minus;1.5. There was a distinct seasonal pattern with peak loadings in January, when bird abundances were highest. Lowest inputs were in August, when bird abundance and nutrient content in food was low and birds foraged less in terrestrial habitats. Three-quarters of all nutrient input was contributed by greater white-fronted goose Anser albifrons, greylag goose Anser anser, wigeon Anas penelope and barnacle goose Branta leucopsis alone.6. We provide general, easy to use calculation methods for the estimation of allochthonous nutrient inputs by waterbirds, which are applicable to a range of waterbird species, a variety of potential diets and feeding behaviours, and across spatial scales. Such tools may greatly assist in the planning and execution of management actions for wetland nutrient budgets.<br /
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