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7 results for “stable isotope mixing models”
Stable Isotope Mixing Models Demonstrate the Role of an Invasive Plant in Wetland Songbirds Food Webs
<p>We used analysis of natural abundance stable isotopes of <sup>13</sup>C and <sup>15</sup>N in song sparrow blood, invertebrate food sources, <em>L. latifolium </em>seeds,<em> </em>and other marsh<em> </em>plant seeds to inform Bayesian, concentration-dependent mixing models that predicted average song sparrow diets. Data presented are the csv files and R markdown code for the isotope analysis.</p>
Dataset: Testing for effects of growth rate on isotope trophic discrimination factors and evaluating the performance of Bayesian stable isotope mixing models experimentally: a moment of truth?
<p><span>Discerning assimilated diets of wild animals using stable isotopes is well established where potential dietary items in food webs are isotopically distinct. With the advent of mixing models, and Bayesian extensions of such models (Bayesian Stable Isotope Mixing Models, BSIMMs), statistical techniques available for these efforts have been rapidly increasing. The accuracy with which BSIMMs quantify diet, however, depends on several factors including uncertainty in tissue discrimination factors (TDFs; <em>Δ</em>) and identification of appropriate error structures. Whereas performance of BSIMMs has mostly been evaluated with simulations, here we test the efficacy of BSIMMs by raising domestic broiler chicks (<em>Gallus gallus domesticus</em>) on four isotopically distinct diets under controlled environmental conditions, ideal for evaluating factors that affect TDFs and testing how BSIMMs allocate individual birds to diets that vary in isotopic similarity. For both liver and feather tissues,<em> δ</em><sup>13</sup>C and <em>δ </em><sup>15</sup>N values differed among dietary groups. <em>Δ</em><sup>13</sup>C of liver, but not feather, was negatively related to the rate at which individuals gained body mass. For <em>Δ</em><sup>15</sup>N, we identified effects of dietary group, sex, and tissue type, as well as an interaction between sex and tissue type</span><span><span>, </span></span><span><span>with f</span></span><span>emales having higher liver <em>Δ</em><sup>15</sup>N relative to males. For both tissues, BSIMMs allocated most chicks to correct dietary groups, especially for models using combined TDFs rather than diet specific TDFs, and those applying a multiplicative error structure. These findings provide new information on how biological processes affect TDFs and confirm that adequately accounting for variability in consumer isotopes is necessary to optimize performance of BSIMMs. Moreover, they demonstrate experimentally that these types of models reliably characterize consumed diets when appropriately parameterized.<span> </span></span></p>
Bayesian stable isotope mixing models effectively characterize the diet of an Arctic raptor
<p>1. Bayesian stable isotope mixing models (BSIMMs) for δ13C and δ15N can be a useful tool to reconstruct diets, characterize trophic relationships, and assess spatiotemporal variation in food webs. However, use of this approach typically requires a priori knowledge on the level of enrichment occurring between the diet and tissue of the consumer being sampled (i.e., a trophic discrimination factor or TDF).</p> <p>2. TDFs derived from captive feeding studies are highly variable, and it is challenging to select the appropriate TDF for diet estimation in wild populations. We introduce a novel method for estimating TDFs in a wild population: a proportionally balanced equation that uses high-precision diet estimates from nest cameras installed on a subset of nests in lieu of a controlled feeding study (TDFCAM).</p> <p>3. We tested the ability of BSIMMs to characterize diet in a free-living population of gyrfalcon (Falco rusticolus) nestlings by comparing model output to high-precision nest camera diet estimates. We analyzed the performance of models formulated with a TDFCAM against other relevant TDFs and assessed model sensitivity to an informative prior. We applied the most parsimonious model inputs to a larger sample to analyze broad-scale temporal dietary trends.</p> <p>4. BSIMMs fitted with a TDFCAM and uninformative prior had the best agreement with nest camera data, outperforming TDFs derived from captive feeding studies. BSIMMs produced with a TDFCAM produced reliable diet estimates at the nest level and accurately identified significant temporal shifts in gyrfalcon diet within and between years.</p> <p>5. Our method of TDF estimation produced more accurate estimates of TDFs in a wild population than traditional approaches, consequently improving BSIMM diet estimates. We demonstrate how BSIMMs can complement a high-precision diet study by expanding its spatiotemporal scope of inference and recommend this integrative methodology as a powerful tool for future trophic studies. </p>
Evaluating Bayesian stable isotope mixing models of wild animal diet and the effects of trophic discrimination factors and informative priors
<blockquote> <p>1. Ecologists quantify animal diets using direct and indirect methods, including analysis of faeces, pellets, prey items and gut contents. For stable isotope analyses of diet, Bayesian stable isotope mixing models (BSIMMs) are increasingly used to infer the relative importance of food sources to consumers. Although a powerful approach, it has been hard to test BSIMM performance for wild animals because precise, direct dietary data are difficult to collect.<br> 2. We evaluated the performance of BSIMMs in quantifying animal diets when using δ13C and δ15N stable isotope ratios from the feathers and red blood cells of common buzzard Buteo buteo chicks. We analysed mixing model outcomes with various trophic discrimination factors (TDFs), with and without informative priors, and compared these to direct observations of prey provisioned to chicks by adults at nests, using remote cameras. <br> 3. Although BSIMMs with different TDFs varied markedly in their performance, the statistical package SIDER generated TDFs for both feathers and blood that resulted in model outputs that accorded well with direct observations of prey provisioning. Using feather TDFs derived from captive peregrines Falco peregrinus resulted in estimates of diet composition that were also similar to provisioned prey, though blood TDFs from the same study performed poorly. The inclusion of informative priors, based on conventional analysis of pellet and prey remains, markedly reduced model performance.<br> 4. BSIMMs can provide accurate assessments of diet in wild animals. TDF estimates from the SIDER package performed well. The inclusion of informative priors from conventional methods in Bayesian mixing models can transfer biases into model outcomes, leading to erroneous results.</p> </blockquote>
Dataset and codes used in the manuscript entitled "A rainfall-tracking travel time distribution model to quantify mixing and storage release preference in a large shallow lake by two-year stable isotopic data"
<p>This contains the codes and dataset for the manuscript entitled "A rainfall-tracking travel time distribution model to quantify mixing and storage release preference in a large shallow lake by two-year stable isotopic data". Detailed information about the dataset is described in the Readme.txt file.</p>
Data from: Evaluating Bayesian stable isotope mixing models of wild animal diet and the effects of trophic discrimination factors and informative priors
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Bayesian stable isotope mixing models effectively characterize the diet of an Arctic raptor
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