Jesus Fabiene Maria, Pereira Marcelo Ribeiro, Rosa Cassiano Sousa, Moreira Marcelo Zacharias, Sperber Carlos Frankl
Programa de Pós-graduação em Ecologia, Departamento de Biologia Geral, Universidade Federal de Viçosa, Viçosa, MG, Brazil.
Universidade Federal do Espírito Santo, Centro de Ciências Agrárias, Departamento de Biologia, Alegre, ES, Brazil.
PLoS One. 2015 Sep 21;10(9):e0137650. doi: 10.1371/journal.pone.0137650. eCollection 2015.
Stable isotope analysis (SIA) is an important tool for investigation of animal dietary habits for determination of feeding niche. Ideally, fresh samples should be used for isotopic analysis, but logistics frequently demands preservation of organisms for analysis at a later time. The goal of this study was to establish the best methodology for preserving forest litter-dwelling crickets for later SIA analysis without altering results. We collected two cricket species, Phoremia sp. and Mellopsis doucasae, from which we prepared 70 samples per species, divided among seven treatments: (i) freshly processed (control); preserved in fuel ethanol for (ii) 15 and (iii) 60 days; preserved in commercial ethanol for (iv) 15 and (v) 60 days; fresh material frozen for (vi) 15 and (vii) 60 days. After oven drying, samples were analyzed for δ15N, δ13C values, N(%), C(%) and C/N atomic values using continuous flow isotope ratio mass spectrometry. All preservation methods tested, significantly impacted δ13C and δ15N and C/N atomic values. Chemical preservatives caused δ13C enrichment as great as 1.5‰, and δ15N enrichment as great as 0.9‰; the one exception was M. doucasae stored in ethanol for 15 days, which had δ15N depletion up to 1.8‰. Freezing depleted δ13C and δ15N by up to 0.7 and 2.2‰, respectively. C/N atomic values decreased when stored in ethanol, and increased when frozen for 60 days for both cricket species. Our results indicate that all preservation methods tested in this study altered at least one of the tested isotope values when compared to fresh material (controls). We conclude that only freshly processed material provides adequate SIA results for litter-dwelling crickets.
稳定同位素分析(SIA)是研究动物饮食习惯以确定觅食生态位的重要工具。理想情况下,应使用新鲜样本进行同位素分析,但实际操作中,由于后勤原因,常常需要保存生物体以便日后分析。本研究的目的是建立一种最佳方法,用于保存森林落叶层中的蟋蟀,以便日后进行SIA分析而不改变结果。我们收集了两种蟋蟀,即Phoremia sp.和Mellopsis doucasae,每种蟋蟀制备了70个样本,分为七种处理方式:(i)新鲜处理(对照);保存在燃料乙醇中(ii)15天和(iii)60天;保存在商业乙醇中(iv)15天和(v)60天;新鲜材料冷冻(vi)15天和(vii)60天。烘干后,使用连续流同位素比率质谱仪分析样本的δ15N、δ13C值、N(%)、C(%)和C/N原子值。所有测试的保存方法均对δ13C、δ15N和C/N原子值产生了显著影响。化学防腐剂导致δ13C富集高达1.5‰,δ15N富集高达0.9‰;唯一的例外是保存在乙醇中15天的M. doucasae,其δ15N贫化高达1.8‰。冷冻分别使δ13C和δ15N贫化高达0.7‰和2.2‰。两种蟋蟀保存在乙醇中时C/N原子值降低,冷冻60天时C/N原子值升高。我们的结果表明,与新鲜材料(对照)相比,本研究中测试的所有保存方法至少改变了一个测试的同位素值。我们得出结论,只有新鲜处理的材料才能为落叶层蟋蟀提供足够的SIA结果。