Anais da Academia Brasileira de Ciências (2013) 85(1): 245-256 (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 www.scielo.br/aabc Brachyuran and anomuran crabs associated with Schizoporella unicornis (Ectoprocta, Cheilostomata) from southeastern Brazil DOUGLAS F.R. ALVES1,2,3, SAMARA P. BARROS-ALVES1,2,3, DANIEL J.M. LIMA1,2,3, VALTER J. COBO2,3 and MARIA LUCIA NEGREIROS-FRANSOZO1,2 1Universidade Estadual Paulista/UNESP, Departamento de Zoologia, Instituto de Biociências, Distrito de Rubião Junior, s/n, 18618-970 Botucatu, São Paulo, Brasil 2NEBECC Study Group on Crustacean Biology, Ecology and Culture, Distrito de Rubião Junior, s/n, 18618-970 Botucatu, São Paulo, Brasil 3Laboratório de Biologia Marinha, LabBMar, Instituto de Biociências, Universidade de Taubaté/UNITAU, Av. Tiradentes, 500, Centro, 12030-180 Taubaté, SP, Brasil Manuscript received on August 23, 2011; accepted for publication on April 27, 2012 ABSTRACT The main goals of this investigation were to describe the community structure of anomuran and brachyuran crabs inhabiting reefs constituted by colonies of Schizoporella unicornis, and to provide a species importance ranking for this community. Collections were carried out on S. unicornis reefs at two-month intervals from May 2003 to May 2004, in the rocky sublittoral of the southeastern Brazilian coast. Relative abundance and occurrence were used to rank these species in the hierarchy importance. A total of 2,018 individuals were obtained, in 11 families, 22 genera and 31 species. Porcellanidae and Pilumnidae were the most abundant families, comprising respectively almost 60% and 15% of individuals sampled. The species ranking indicated four main groups A, B, C and D, with group A subdivided. Subgroup A1 contained 9 species, including the species of greatest ecological importance for community regarding abundance and occurrence. The great abundance of crabs associated with S. unicornis seems to be the result of its recognized importance during the crab developmental cycle, and as shelter and food for some Decapod species. These observations reveal the importance of conserving the areas occupied by these reef colonies, which appear to be an important environment for maintaining local biodiversity. Key words: biogenic substrata, bryozoan, community structure, decapods, symbiotic species. INTRODUCTION habitats, the associated fauna find shelter and food Sessile invertebrates including some corals, and thus a safe site for reproduction and development ectoprocts, polychaetes and mollusks are commonly (Safriel and Eliahu-Ben 1991, Porras et al. 1996). recognized as biogenic substrata builders, which are Decapods occur in association with certain exploited by a large epibiont fauna (Gore et al. 1978, sessile invertebrates such as sponges (Porras et al. Bradstock and Gordon 1983, Safriel and Ben-Eliahu 1996, Caruso et al. 2005), corals and anemones 1991, Thompson et al. 1996). On these biogenic (Humes 1991, Arvanitides and Koukouras 1994), worm tubes (Nalesso et al. 1995, Sepúlveda et al. Correspondence to: Samara de Paiva Barros-Alves E-mail: [email protected] 2003, Nascimento and Torres 2006), echinoderms An Acad Bras Cienc (2013) 85 (1) 246 DOUGLAS F.R. ALVES et al. (Wirtz et al. 2009) and bryozoans (Ferdeghini et This contribution characterizes the community al. 2000, Morgado and Tanaka 2001). However, structure of the anomuran and brachyuran crabs some decapod groups seem to be preferentially living on reefs of S. unicornis in a small bay on associated with certain biogenic substrata, where the southeastern Brazilian coast. The following they can reach high abundances, which may population parameters of decapods were also mean a close relationship among these associated analyzed: abundance, occurrence, size and sex species (e.g., sponges with pilumnid crabs and ratio. In order to evaluate the symbiotic species alpheid shrimps; Sargassum beds with epialtid with S. unicornis, the level of importance to crabs; Phragmatopoma reefs with porcellanid this community was evaluated by means of the crabs, among others) (Micheletti-Flores and occurrence and relative abundance of the species. Negreiros-Fransozo 1999, Széchy et al. 2001, MATERIALS AND METHODS Bosa and Masunari 2002, Ribeiro et al. 2003). Exact knowledge of which species are involved Collections of S. unicornis reefs were carried out at in these symbiotic relationships could provide two-month intervals from May 2003 to May 2004. biological and ecological information concerning The reefs studied were growing on pier columns at these decapods, and also regarding the traits of the Itaguá Beach in Ubatuba, northeastern coast of São supposed dependence relationships between the Paulo State (23°27’04”S-45°02’49”W) (Fig. 1). The decapods and their biogenic substrata. reefs were collected by hand, by divers working Species of the genus Schizoporella Hincks, during the daytime. The catch per unit effort 1877 are bryozoan ectoprocts of the family consisted of one person scanning the bottom for Schizoporellidae, which build calcareous reefs on reefs, for each two months. hard substrates, forming shelters for a variety of The material (bryozoan colonies) collected invertebrate fauna, including decapod crustaceans. was bagged during the dive to avoid the loss of Some investigators have reported on these specimens, and transferred to the Marine Biology associations involving decapods and Schizoporella Laboratory at the Universidade de Taubaté – reefs, mainly on United States and Brazilian coasts, such as Lindberg (1980), Lindberg and Frydenborg (1980), Lindberg and Stanton (1988, 1989), Mantelatto and Souza-Carey (1998a, b) and Morgado and Tanaka (2001). Schizoporella unicornis (Johnston 1847) is a sessile cosmopolitan bryozoan, it is distributed along the Brazilian coast with records in Northeast, Southeast and South (Farrapeira 2011). The colonies of S. unicornis have an orange structure with a variety of branched shapes, occurring due to interactions with other organisms and the local hydrodynamic condition (Cocito et al. 2000, Ferdeghini et al. 2000). These colonies grow in intertidal zones, on rocky substrates or on pier columns, and can reach up to 25 cm height (Ross and McCain 1976). Fig. 1 - Map of the northeastern coast of São Paulo showing Itaguá Beach. An Acad Bras Cienc (2013) 85 (1) BRACHYURANS AND ANOMURANS ASSOCIATED WITH S. unicornis 247 UNITAU, where the decapods were separated from RESULTS the colonies. The crabs were identified according to Melo (1996, 1999), and their classification followed During the field surveys, 2,018 individuals were Ng et al. (2008). collected, distributed in 11 families, 22 genera and Sex and developmental stage (juvenile or 31 species of anomuran and brachyuran decapods. adult) of the brachyuran crabs were identified Identification at species level was not possible from the external morphology of the abdomen for 78 specimens, which were recognized only to and appendages. The sex determination for family level (Table I). The porcellanid anomuran anomurans was based on the gonopore position crabs Megalobrachium roseum, Pachycheles (females on the coxa of the third pereiopod monilifer and Pisidia brasiliensis were the most and males on the coxa of the fifth pereiopod), abundant species, with 409, 297 and 179 individuals and the individuals were identified as juvenile captured, respectively. The brachyuran crabs Pelia or adult considering the size of the smallest rotunda, Microphrys antillensis, Hexapanopeus ovigerous females obtained in the samples. For paulensis, and the anomuran crab Calcinus tibicen, those species, which no ovigerous females was Pachycheles riisei and Petrolisthes amoenus were recorded, the size of smallest ones obtained represented by only one specimen each (Table I). by Litulo (2005) and Miranda and Mantelatto The most abundant families were Porcellanidae (2009) was used. The sex ratio was estimated and and Pilumnidae, comprising respectively around tested by Chi-square (p < 0.05) (Zar 1999). The 60% and 15% of the total decapods collected. These largest carapace width (CW) was measured for porcellanid crabs also showed the highest species brachyuran and porcellanid crabs, and the shield richness, contributing 9 of the total species found in length (SL) for hermit crabs. association with the reef colonies (Table I). The relative abundance (RAb) was calculated The species ranking indicated four groups (A, for each crab species as RAb = n/N, where n = total B, C, and D) composed of 15, 3, 5 and 8 species absolute abundance recorded for a given species, respectively. Group A was subdivided into subgroups and N = total of the individuals recorded over the A1 and A2 (Fig. 2). The species belonging to groups entire sampling program. The relative occurrence C and D showed the lowest relative abundance and (RO) was represented as RO = p/P, where p occurrence, while group B species were recorded in = number of samples containing in the given intermediate abundance and occurrence, and species species, and P = the total number of samples. In of group A were the most important in relative order to estimate the similarity of species present abundance and occurrence. in the community, these species were grouped Subgroup A1 was composed of 9 species, according to Bray-Curtis similarity index, Megalobrachium roseum, Pachycheles monilifer, followed by UPGMA cluster method (Zar 1999), Petrolisthes galathinus, Pisidia brasiliensis, where the indexes (RAb
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