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Brazilian Journal of Oceanography

On-line version ISSN 1982-436X

Braz. j. oceanogr. vol.58 no.spe3 São Paulo June 2010

http://dx.doi.org/10.1590/S1679-87592010000700003 

Biological features on epibiosis of Amphibalanus improvisus (Cirripedia) on Macrobrachium acanthurus (Decapoda)*

 

 

Cristiane Maria Rocha FarrapeiraI,**; Tereza Cristina dos Santos CaladoII

IUniversidade Federal Rural de Pernambuco – UFRPE, Departamento de Biologia, (Rua Dom Manoel de Medeiros, s/nº, 52-171-900 Recife, PE, Brasil)
IIUniversidade Federal de Alagoas – UFAL, Laboratório Integrado de Ciências do Mar e Naturais, (Rua Aristeu de Andrade, 452, 57051-090 Maceió, AL, Brasil)

 

 


ABSTRACT

This study aimed to describe the epibiosis of barnacles Amphibalanus improvisus on eight adult Macrobrachium acanthurus males from the Mundaú Lagoon, state of Alagoas, Brazil. The number of epibiont barnacles varied from 247 to 1,544 specimens per prawn; these were distributed predominantly on the cephalothorax and pereiopods, but also on the abdomen and other appendices. Although some were already reproducing, most barnacles had been recruited recently or were still sexually immature; this suggests recent host arrival in that estuarine environment. Despite the fact that other barnacles occur in this region, A. improvisus is the only species reported as an epibiont on Macrobrachium acanthurus; this was also the first record of epibiosis on this host. The occurrence of innumerable specimens in the pereiopods' articulations and the almost complete covering of the carapace of some prawns (which also increased their weight) suggest that A. improvisus is adapted to fixate this kind of biogenic substrate and that the relationship between the two species biologically damages the basibiont.

Descriptors: Barnacle, Prawn, Estuary, Epibiosis, Commensalism.


RESUMO

O objetivo deste trabalho foi relatar a epibiose de cirrípedes Amphibalanus improvisus em oito camarões machos adultos da espécie Macrobrachium acanthurus provenientes da Laguna Mundaú, Alagoas, Brasil. O número de cirrípedes epibiontes variou desde 247 até 1.544 espécimes por camarão, distribuídos predominantemente no cefalotórax e pereiópodos, mas presentes também no abdome e demais apêndices. A grande maioria dos cirrípedes era recém-recrutada ou ainda estava sexualmente imatura, embora de alguns estivessem já em reprodução, sugerindo a chegada recente de seu hospedeiro no ambiente estuarino. Apesar de ocorrem outros cirrípedes na região, A. improvisus foi à única espécie relatada como epibionte em Macrobrachium acanthurus e isto se constituiu o primeiro registro de epibiose de Amphibalanus improvisus A ocorrência de inúmeros espécimes nas articulações dos pereiópodos e o recobrimento quase total da carapaça de alguns camarões (incrementando peso aos mesmos) indicam que a espécie epibionte está adaptada à fixação neste substrato biogênico e que a relação entre estas duas espécies traz prejuízos biológicos ao basibionte.

Descritores: Cirrípede, Camarão, Estuário, Epibiose, Comensalismo.


 

 

INTRODUCTION

Macrobrachium acanthurus (Wiegmann, 1836), locally known as the cinnamon prawn or "pitu", inhabits fresh and brackish waters of coastal rivers and bays freely connected to the sea, and is distributed from North Carolina to southern Brazil (COELHO and RAMOS-PORTO, 1985; ABELE and KIM, 1986; VALENTI et al., 1989; SIGNORET and BRAILOVSKY, 2004). This edible prawn is the basis of small fisheries exploited by several human communities close to estuaries, and is an economically important natural resource. Due to its size, high fertility and fecundity rates, easy maintenance and reproduction in laboratory conditions, and good acceptance on the consumer market, it is also considered a species with cultivation potential on a commercial scale (CHOUDHURY, 1970; NEW, 1995; RAMOS-PORTO, 1980; COELHO and RAMOS-PORTO, 1985; SOUSA and CALADO, 1998; QUADROS et al., 2004).

In the state of Alagoas, northeastern Brazil, M. acanthurus is found in the shallow waters of the Mundaú/Manguaba lagoon system, where it is a dominant species in number and biomass and occurs throughout the year at most stations (COELHO et al., 1990; TEIXEIRA and SÁ, 1998; SOUSA et al., 2000; CALADO and SOUSA, 2003). It is one of the most exploited prawns and is usually sold in urban centers.

The finding of some male specimens severely fouled by barnacles in the Mundaú Lagoon during a bioindicator project has received much attention; according to local vendors, these specimens have completely lost their commercial value. This study aimed, therefore, to record and investigate the relationship between the prawn Macrobrachium acanthurus and its epibiont barnacle species and to quantitatively describe the abundance and spatial distribution of ectosymbionts.

 

MATERIAL AND METHODS

The Mundaú Lagoon (with an area of 24 km2), located in the neighborhood of Pilar (a town near Maceió, Alagoas, Northeast Brazil), is part of the Mundaú/Manguaba complex (9º36'S - 9º45'S, 35º41'W - 35º55'W), which in turn receives its main freshwater input from the Mundaú River. It is connected to the Atlantic Ocean and the Manguaba Lagoon by a network of channels (OLIVEIRA and KJERFVE, 1993; NORMANDE, 2000) (Fig. 1). Air temperature varies from an average of 30.1ºC in the dry season to 20.8ºC in the wet season, when salinity is around zero (MACÊDO et al., 1987; NORMANDE, 2000).

 

 

As part of another study, which aimed to analyze the quantities of heavy metals and the ecotoxicology of invertebrates in the Mundaú/Manguaba complex, 21 prawns were collected by a fisherman in February 2008 near the margins of the Mundaú lagoon. This fisherman used artisanal wooden traps baited with cassava. Of the total, eight male prawns hosting macro-epibiont barnacles were brought to the laboratory for closer examination (the remaining prawns were used for the ecotoxicology and heavy metal analysis). A stereomicroscope and optical microscopes were used to identify and count the number of epibiont individuals. The presence of other symbiotic species (colonies) was also reported and their position on the prawns registered.

The prawns' carapace length (rostrum to telson) and barnacles' carinorostral diameter (carina to rostrum plates) were measured using a caliper (mm). The epibiont barnacles were counted directly on the carapaces using a stereomicroscope and insoluble paint/dye to mark the individuals counted. The counting was repeated three times and when the data disagreed an average number was taken. The number of specimens on each area of the prawn is presented and, for statistical analyses, also grouped according to their occurrence on two main regions and three groups of appendages. The two regions were the cephalothorax carapace (including rostrum) and the abdomen (including telson), while the three groups of appendages included the cephalic (including the ocular peduncles and the ocular orbit itself); thoracic and abdominal appendages. The barnacles on the ventral region were also counted. Statistical analyses (Friedman and the Wilcoxon signed-rank tests) were carried out to relate the various anatomical units of the crab to the epibionts. Digital images of organisms were registered using a Sony Cyber-shot DSC-W35 camera, some images also being obtained through a dissecting microscope lens. Voucher prawn specimens and their symbiotic species have been deposited in the respective taxonomic Crustacea (Universidade Federal de Alagoas – CC07773) and Cirripedia collections (Universidade Federal Rural de Pernambuco – DBUFRPE n. 1132).

 

RESULTS

The barnacle A. improvisus was present on all the male prawn specimens (mean carapace length of 14.98 ± 0.10 cm). In addition to the barnacle Amphibalanus improvisus (Darwin, 1854), the main epibiont species, two other unidentified commensals were found: a Vesiculariidae bryozoan and a Sertulariidae hydrozoan. The Vesiculariidae bryozoan colonies covered the cuticle of a single prawn (specimen 8), where it formed a network of thin stolons fixed on the carapace like armor intercalated within the barnacle's shells They also fouled the entire cephalothoracic carapace (including the rostrum and basal articles of antennas), three abdominal somites, four pereiopods, two pleopods, and the uropods, as well as the ventral cephalothoracic and abdominal areas, between the appendices (Fig. 2). The hydrozoans consisted of short dead stalks without hydrants and were found on two prawns (specimens 5 and 6), solely on the second and third pereiopods (Fig. 3).

 

 

 

 

The number of barnacles attached to each prawn ranged from 247 large individuals (specimen 1) to 1,544 smaller ones (specimen 8). Table 1 lists the number of barnacles present on each of the different body regions and appendages. In most thoracic and abdominal appendices, barnacles occurred mainly on the coxopodit and basipodit. Few barnacles were attached laterally onto the pleura or on the mid-dorsal line of the abdominal segments. The barnacles' settling areas included the ocular orbit and peduncle (Fig. 3b, 4b), the antenna's flagellum, the sexual appendage, and several furrows of the articulations (Fig. 4c, 4e). Ecomorphosis was observed for the barnacles that grew among the spines and setae of the second pereiopods; in this case, the basal margin of their shell had unusual hollows (Fig. 4d).

 

 

 


 

As regards the various body regions, the cephalothoracic carapace was the main settlement area, with the dorsal carina surface (dorsum) as the main site (Fig. 3b, 4a). Among the body appendages, barnacles preferred the thoracic ones (especially the pereiopods) and were more numerous on the second pereiopod (Fig. 4c) for those specimens that still had it (740 animals on specimen 2's pair) (Table 1). When comparing barnacle counts across these two regions and the three types of appendages, significant differences were only found between the cephalothoracic carapace and the abdominal appendages (Friedman test, df D= 21.5; P < 0.05) and between the thoracic and abdominal appendages (Friedman test, df D=19; P < 0.05). A significant difference was also observed among the barnacles' settlement patterns – far more were attached to the cephalothoracic carapace than to the abdominal somites (Wilcoxon signed-rank test, P= 0.0357).

Most of these barnacles were recent recruits or still sexually immature, although some specimens were adults (Fig. 4a), were in reproduction, had well developed gonads, and were even incubating eggs. The carinorostral diameter of most young barnacles was of 1.7 ± 1.1 mm. The diameter of the largest specimens examined was of 4.1 ± 2.1 mm (measurements of the mature specimens, settled mainly on the surface of the dorsal carina).

 

DISCUSSION

It was not a surprise to find three epibiont species on prawn surfaces. The lack of available hard and stable substrate is often a limiting factor for fouling organisms, especially in estuarine areas with muddy bottoms like the Mundaú Lagoon. The calcified carapaces of decapod crustaceans appear to be one of the few suitable mobile habitats for epibiont attachment in this type of inhospitable, soft sediment bottom, as pointed out by Ross (1983) and Gili et al. (1993). Furthermore, despite its relatively short lifespan due to moulting (shedding of the crab's exoskeleton), many organisms (protozoans, algae, barnacles, bryozoans, hydrozoans, bivalves) use this substratum as an alternative hard substrata (ABELLÓ and CORBERA, 1996).

Several studies have reported the barnacle Amphibalanus improvisus as an epibiont organism. Dawson (1957) found it on the white shrimp Penaeus setiferus (Linnaeus, 1767) of the inshore waters of Mississippi and South Carolina; Eldred (1962) recorded it attached to the exoskeletons of the rock shrimp Sicyonia dorsalis from the Tortugas shrimping grounds, where some also hosted unidentified hydroids; and Giri and Wicksten (2002) collected the fouled peppermint shrimp Lysmata wurdemanni (Gibbes, 1850) in Texas. As regards the barnacle-shrimp relationship, all these authors also observed that the carapace's dorsolateral surface was the main area of barnacle settlement. Amphibalanus improvisus has been also recorded as an episymbiont on other vagile crustaceans, such as the portunids Callinectes danae Smith, 1869 and C. larvatus Ordway, 1863 (FARRAPEIRA, 2006); the crabs Hemigrapsus sanguineus (De Haan, 1853) (McDERMOTT, 2007), Libinia spinosa Milne Edwards 1834, Neohelice (Chasmagnathus) granulata (Dana, 1851), and Platyxanthus crenulatus A. Milne-Edwards, 1879 (SPIVAK, 2003); and the crayfishes Astacus leptodactylus (Eschscholtz, 1823) (LAMANOVA, 1970) and Pacifastacus trowbridgii (Stimpson, 1857) (COHEN, 1995). It has also been recorded on gorgonians, mollusks, and other barnacles (SILVA-BRUM and MARTINS, 1996; FARRAPEIRA, 2006, 2008). This is the first record of Amphibalanus improvisus on Macrobrachium acanthurus.

The location of the main barnacle aggregations is not casual, as defense mechanisms against epibionts would be expected if the disadvantages suffered by the host outweighed the benefits (BECKER, 1996). Antifouling strategies such as grooming are partial adaptations to the need to keep the cuticle free of fouling organisms. In caridean species observed preening the body, one of the two pairs of chelipeds is characteristically involved in grooming, as well as its long antennae. Pereiopods used in preening are usually the most slender of the two pairs and bear dense tufts of serrate or multiscaled setae and interdigitating stout setae on the tips of the chelal fingers (BAUER, 1978). In the case of Macrobrachium males – which have unusually enlarged second chelae – these are used in agonistic interactions and predation (GRAVE et al., 2008).

Particular features of epibiosis can provide useful correlative information on the biological and behavioral characteristics of the host (ABELLÓ and CORBERA, 1996; KEY et al., 1996; 1999). There are several considerations that should be borne in mind regarding the relationship between barnacles and prawns. Macrobrachium acanthurus lives preferentially in fresh water and occasionally migrates to brackish waters (COELHO and RAMOS-PORTO, 1985), despite being considered a hyperosmotic regulator in salinities between 0 and 20 (SIGNORET and BRAILOVSKY, 2004). Teixeira and Sá (1998), for instance, have reported that it prefers the fresher waters in the Mundaú/Manguaba lagoonal complex; thus, according to those authors, it only swims into the lagoon proper between July and October, and then only to places where the salinity is less than 5. The migration of adults to the estuary occurs during the reproductive season – spring and summer (JALIHAL et al., 1993; BOND-BUCKUP and BUCKUP, 1999; MEJÍA-ORTÍZ et al., 2001). According to Boschi (1974), most species of this genus lay their eggs in brackish water, and adults and larvae need the salinity to complete the reproductive cycle.

The prawns' migratory behavior to the estuarine areas and the fact that it stops for considerable periods of time to perform grooming and cleaning activities (BAUER, 1975) possibly allowed for barnacle larvae to settle on their exoskeleton. Amphibalanus improvisus has previously been recorded in the low salinity area of the Mundaú/Manguaba lagoonal complex (CORREIA, 1998; CALADO and SOUSA, 2003) and has low salinity acclimation (as low as 1-2) (NEWMAN, 1967; FOSTER, 1970; KENNEDY and DICOSIMO, 1983). Its metamorphosis is completed within 8-16 h after permanent attachment (GLENNER and HOEG, 1993).

The short cycle of the barnacle species must also be highlighted, as it is a crucial factor for animals that live on such temporary substrates. Although the frequent molting of caridean prawns does remove all fouling, there might be periods in some species' life cycles when the molting rate is low enough to allow for extensive fouling (e.g., when females are carrying embryos) (FELGENHAUER and SCHRAM, 1979). According to these authors, the normal physiology of prawns is continuously involved in the successive stages of the molting cycle. However, this can be interrupted periodically by gonad maturation, which coincides with the period of migration into the estuary. Since fouling can occur only during interecdysal periods, the barnacles must have developed between the previous molting event and the moment of capture. Dawson (1957) also observed this fact by looking at the time A. improvisus appeared on the penaeid shrimp Penaeus setiferus, when fouling by maturing barnacles was probably confined to this period of reduced molting frequency.

The degree of epibiosis is another aspect to be considered about this symbiotic relationship. The body design of carideans and other natantian decapods consists of a set of adaptations for swimming, particularly the subcylindrical and generally smooth cephalothorax, the flattened antennae scales (that serve as horizontal rudders for control during the escape response), and the long, laterally compressed rostrum that acts as a stabilizing keel (BAUER, 1978). The rugosity of the barnacle shells results in many disadvantages due to the higher energy cost required for movement. Furthermore, the added weight of the attached barnacles on the heavily encrusted prawn and the overlap of the larger barnacles on the body segments undoubtedly interfere with the prawns' natural movement and acceleration and, thus, make it more susceptible to predation (ELDRED, 1962; WAHL, 1989). Fernandez-Leborans and Gabilondo (2005) report that the presence of epibionts on Liocarcinus depurator (Linnaeus, 1758) and Pilumnus hirtellus (Linnaeus, 1761) negatively impacts the crab, as the added weight and possible impairment of mobility due to changes in the body's hydrodynamic equilibrium can hinder appendage movement.

Anything preventing movement between segments will interfere with the appendages' locomotory and feeding movements and with body's postural changes; this will thus restrict mobility and interfere with swimming. In this study, several barnacle specimens were found growing on pereiopod articulations, covering sensitive organs (eyes, antennae), and even on the sexual appendage. According to Felgenhauer and Schram (1979), this kind of fouling may hinder locomotion or inhibit sensory reception, depending upon the location and intensity of the infestation. Normal fluid flow within the animal may also become impaired, including loss of chemoreception capacity. The occurrence of numerous specimens on pereiopod articulations and the almost complete covering of some prawns' carapace (in addition to the added weight) indicates that the epibiont barnacle species are adapted for settling on this biogenic substratum. Additionally, the consequent biological damage caused to the basibiont suggests that the relationship between these two species is not simply one of commensalism.

 

ACKNOWLEDGMENTS

The authors are grateful to Liliane Tonial and Carlos de Carvalho Veiga who gave us the fouled prawn specimens collected during their project the purpose of which was to assess the impact of pollutants from sugarcane monocultures in the estuaries and coastal waters of Alagoas (Marine Sciences Program – POCALMAR, a bilateral agreement between Brazil and Germany). Special thanks also go to Débora Barbosa, for her valuable help in the statistical analyses, to Andrea Steiner for helping with the English version, and to the anonymous reviewers for their comments.

 

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(Manuscript received 26 February 2009; revised 23 April 2010; accepted 27 April 2010)

 

 

* Paper presented at the Brazilian Symposium of Oceanography, 4., 2008, São Paulo, IOUSP.
** c.farrapeira@db.ufrpe.br

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