Abstract

Ecologists have been largely interested in the description and understanding of the power scaling relationships between body size and abundance of organisms. Many studies have focused on estimating the exponents of these functions across taxonomic groups and spatial scales, to draw inferences about the processes underlying this pattern. The exponents of these functions usually approximate -3/4 at geographical scales, but they deviate from this value when smaller spatial extensions are considered. This has led to propose that body size-abundance relationships at small spatial scales may reflect the impact of environmental changes. This study tests this hypothesis by examining body size spectra of benthic shrimps (Decapoda: Caridea) and snails (Gastropoda) in the Tamiahua lagoon, a brackish body water located in the Eastern coast of Mexico. We mea- sured water quality parameters (dissolved oxygen, salinity, pH, water temperature, sediment organic matter and chemical oxygen demand) and sampled benthic macrofauna during three different climatic conditions of the year (cold, dry and rainy season). Given the small size of most individuals in the benthic macrofaunal samples, we used body volume, instead of weight, to estimate their body size. Body size-abundance relationships of both taxonomic groups were described by tabulating data from each season into base-2 logarithmic body size bins. In both taxonomic groups, observed frequencies per body size class in each season were standardized to yield densities (i.e., individuals/m(3)). Nonlinear regression analyses were separately performed for each taxonomic group at each season to assess whether body size spectra followed power scaling functions. Additionally, for each taxonomic group, multiple regression analyses were used to determine whether these relationships varied among seasons. Our results indicated that, while body size-abundance relationships in both taxonomic groups followed power functions, the parameters defining the shape of these relationships varied among seasons. These variations in the parameters of the body size-abundance relationships seems to be related to changes in the abundance of individuals within the different body size classes, which seems to follow the seasonal changes that occur in the environmental conditions of the lagoon. Thus, we propose that these body size-abundance relation- ships are influenced by the frequency and intensity of environmental changes affecting this ecosystem.

Highlights

  • Raffaelli, & Edmonds-Brown, 2007; MacNab, 1990; Peters, 1986; White, Ernest, Kerkhoff, & Enquist, 2007)

  • For example, have usually analyzed the frequency distribution of body sizes regardless the species to which organisms belong, or body size spectra, and studies conducted in small water bodies have reported scaling exponents that largely deviate from the expected value of -3/4 (Boix, Sala, Quintana, & Moreno-Amich, 2004; Schmid, Tokeshi, & Schmid-Araya, 2000, 2002)

  • The scaling relationships expected on geographical scales may not be attained at small spatial scales when local species assemblages are affected by external disturbances or cyclical environmental changes

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Summary

Introduction

Raffaelli, & Edmonds-Brown, 2007; MacNab, 1990; Peters, 1986; White, Ernest, Kerkhoff, & Enquist, 2007). Recent studies on benthic macroinvertebrates from Mediterranean lagoons have shown that local body size-abundance relationships can be polygonal in shape, with the highest population density per size class increasing with average individual body size of 0.25 mg and decreasing beyond this threshold (Barbone, Rosati, Pinna, & Basset, 2007; Basset et al, 2008) These differences between observed and expected body size-abundance relationships have been attributed to external disturbances that affect aquatic ecosystems (e.g., seasonal changes in water discharge regimens, anthropogenic disturbances or variations in resource supply rates from terrestrial ecosystems) instead of energetic or resources constraints (Barbone et al, 2007; Basset et al, 2008; Schmid et al, 2000). At small spatial scales, scaling exponents of body size spectra may vary idiosyncratically across time because environmental variability may prevent the community from reaching energetic equilibrium states To test these hypotheses we focused in a coastal brackish lagoon of Mexico that is recurrently affected by seasonal changes in water quality conditions. Body size spectra of these two groups were expected to fit power law functions, but we expected changes in the parameters describing these relationships (a and b) after changes in water quality conditions

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