Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA 15260, USA.
The Cornell Laboratory of Ornithology, Cornell University, Ithaca, NY 14850, USA.
Integr Comp Biol. 2022 Aug 25;62(2):211-222. doi: 10.1093/icb/icac086.
The introduction of laboratory methods to animal dietary studies has allowed researchers to obtain results with accuracy and precision, not possible with observational techniques. For example, DNA barcoding, or the identification of prey with taxon-specific DNA sequences, allows researchers to classify digested prey tissues to the species-level, while stable isotope analysis paired with Bayesian mixing models can quantify dietary contributions by comparing a consumer's isotopic values to those derived from their prey. However, DNA-based methods are currently only able to classify, but not quantify, the taxa present in a diet sample, while stable isotope analysis can only quantify dietary taxa that are identified a priori as prey isotopic values are a result of life history traits, not phylogenetic relatedness. Recently, researchers have begun to couple these techniques in dietary studies to capitalize on the reciprocal benefits and drawbacks offered by each approach, with some even integrating DNA-based results directly into Bayesian mixing models as informative priors. As the informative priors used in these models must represent known dietary compositions (e.g., percentages of prey biomasses), researchers have scaled the DNA-based frequency of occurrence of major prey groups so that their normalized frequency of occurrence sums to 100%. Unfortunately, such an approach is problematic as priors stemming from binomial, DNA-based data do not truly reflect quantitative information about the consumer's diet and may skew the posterior distribution of prey quantities as a result. Therefore, we present a novel approach to incorporate DNA-based dietary information into Bayesian stable isotope mixing models that preserves the binomial nature of DNA-based results. This approach uses community-wide frequency of occurrence or logistic regression-based estimates of prey occurrence to dictate the probability that each prey group is included in each mixing model iteration, and, in turn, the probability that each iteration's results are included in the posterior distribution of prey composition possibilities. Here, we demonstrate the utility of this method by using it to quantify the prey composition of nestling Louisiana waterthrush (Parkesia motacilla).
实验室方法在动物饮食研究中的引入使得研究人员能够以准确性和精密度获得结果,这是观察技术无法做到的。例如,DNA 条形码或使用分类特异性 DNA 序列鉴定猎物,允许研究人员将消化的猎物组织分类到物种水平,而稳定同位素分析与贝叶斯混合模型相结合可以通过将消费者的同位素值与从猎物中得出的同位素值进行比较来量化饮食贡献。然而,基于 DNA 的方法目前只能分类,而不能量化饮食样本中的分类群,而稳定同位素分析只能量化事先确定为猎物的饮食分类群,因为消费者的同位素值是生活史特征的结果,而不是系统发育关系。最近,研究人员开始在饮食研究中结合这些技术,利用每种方法提供的互惠优缺点,有些甚至将基于 DNA 的结果直接整合到贝叶斯混合模型中作为信息先验。由于这些模型中使用的信息先验必须代表已知的饮食组成(例如,猎物生物量的百分比),研究人员已经对基于 DNA 的主要猎物群的出现频率进行了缩放,以便它们归一化的出现频率总和为 100%。不幸的是,这种方法存在问题,因为来自二项式、基于 DNA 的数据的先验并不能真正反映消费者饮食的定量信息,并且可能因此导致猎物数量的后验分布发生偏斜。因此,我们提出了一种将基于 DNA 的饮食信息纳入贝叶斯稳定同位素混合模型的新方法,该方法保留了基于 DNA 的结果的二项式性质。这种方法使用基于群落范围的出现频率或逻辑回归估计的猎物出现来决定每个猎物组在每个混合模型迭代中被包含的概率,进而决定每个迭代的结果在猎物组成可能性的后验分布中被包含的概率。在这里,我们通过使用它来量化巢幼路易斯安那水鸭(Parkesia motacilla)的猎物组成来证明这种方法的实用性。