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Podding of Juvenile King Crabs Lithodes Santolla (Molina, 1782) (Crustacea) in Association with Holdfasts of Macrocystis Pyrifera (Linnaeus) C

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Podding of Juvenile King Crabs Lithodes Santolla (Molina, 1782) (Crustacea) in Association with Holdfasts of Macrocystis Pyrifera (Linnaeus) C Invest. Mar., Valparaíso, 35(1): 105-110, 2007 Podding of juvenile king crabs 105 Nota Científica Podding of juvenile king crabs Lithodes santolla (Molina, 1782) (Crustacea) in association with holdfasts of Macrocystis pyrifera (Linnaeus) C. Agardh, 1980 César A. Cárdenas1, Juan I. Cañete1, Sylvia Oyarzún1 & Andrés Mansilla1 1Departamento de Ciencias y Recursos Naturales, Facultad de Ciencias Universidad de Magallanes, Casilla 113-D, Punta Arenas, Chile ABSTRACT. Underwater photographic records and sampling were carried out in Steamer Bay, Strait of Magellan, Chile, to study the spatial distribution patterns of juvenile king crabs Lithodes santolla during late winter and early spring in 2006. Observations were made on the relationship between these crabs and the holdfasts and stipes of the large kelp Macrocystis pyrifera. Dense aggregations, known as “pods”, of juvenile king crab (34-75 mm CL) were observed and photographed for the first time in specific areas of the embayment in relation to Macrocystis; pod abundance va- ried between 2 and 70 ind·m-2. Maximum abundance was detected on plants having holdfasts > 15 cm in diameter and abundant stipes and sporophylls. The ratio between male and female abundance was nearly 1:1. This study attempts to bring attention to previously unknown ecological roles of the kelp M. pyrifera in relation to its associated benthic fauna in habitats near the southern tip of South America as background information on the ecological functions of this species prior to allowing its industrial-scale exploitation. Key words: subantarctic benthos, seaweed-animal relationship, Lithodes santolla, shallow water, Strait of Magellan, Chile. Agregaciones de juveniles de centolla Lithodes santolla (Molina, 1782) (Crustacea) en asociación con discos de fijación de Macrocystis pyrifera (Linnaeus) C. Agardh, 1980 RESUMEN. Se efectuaron registros fotográficos y colecta de muestras en bahía Steamer, estrecho de Magallanes, Chile, para estudiar los patrones de distribución espacial de juveniles de la centolla Lithodes santolla durante fines de invierno y comienzo de la primavera en 2006. Las observaciones fueron realizadas en relación a presencia de centollas juveniles en discos de fijación y estipes de la macroalga parda Macrocystis pyrifera. Se observaron y fotografiaron por primera vez, densas agregaciones de juveniles de centolla (34-75 mm LC), conocidas como “pods”, en áreas específicas de la bahía relacionadas con Macrocystis. La abundancia varió entre 2 y 70 ind·m-2. Las mayores abundancias se detectaron en plantas con disco de fijación con diámetros > 15 cm y con presencia de abundantes estipes y esporofilas. La propor- ción de abundancia entre machos y hembras fue cercana a 1:1. El presente estudio pretende llamar la atención de los roles ecológicos, previamente desconocidos, del alga M. pyrifera en relación a la fauna bentónica asociada a hábitats distribuidos en el extremo sur de Sudamérica básica para conocer las funciones ecológicas de esta macroalga antes de permitir su explotación a escala industrial. Palabras clave: bentos subantártico, relación alga-animal, Lithodes santolla, aguas someras, estrecho de Magallanes, Chile. Corresponding author: Juan I. Cañete ([email protected]). King crab life-history studies indicate that the early habitats provide refuge from predation by benthic post-settlement age classes exhibit cryptic behavior fishes and invertebrates (Barshaw & Lavalli, 1988) and have restrictive habitat requirements (Lovrich & and the extent and availability of such habitats can Vinuesa, 1995; Loher & Armstrong, 2000). Nursery exert a strong influence on settlement patterns and 106 Investigaciones Marinas, Vol. 35(1) 2007 early post-settlement survival. Thus, the lack of sui- havior has not been reported for southern king crabs. table nursery habitats may define the most restrictive Previously, this type of behaviour has been studied by population “bottleneck” faced by some crustaceans means of direct observations while diving, remotely such as the lobster Homarus americanus and have operated vehicles (ROV) carrying video or still a greater influence on recruitment patterns than do cameras, or submersible vehicles carrying observers absolute levels of larval supply (Wahle & Steneck, (Zhou & Shirley, 1997). In Chile, little work has been 1991). done using underwater images, remote vehicles, and A similar bottleneck may be faced by the Alaskan submersibles, except for the observations of mega- king crab Paralithodes camtschaticus (Loher & benthic communities in the Strait of Magellan by Gutt Armstrong, 2000) and also the subantarctic Lithodes et al. (1999). The present data, obtained by diving, santolla, based on their early life habits. For represents the first observations of the aggregate be- approximately two years post-settlement, termed the haviour of juvenile Lithodes santolla associated with “early benthic phase” (EBP; Wahle & Steneck, 1991), the kelp Macrocystis pyrifera, and our interpretation individual king crabs live a cryptic, solitary existence of its ecological significance. (Karinen, 1985; Stone et al., 1993). The EBP is Field expeditions were made in August and Sep- ecologically distinct from the social-aggregative tember 2006 to observe the benthic behaviour of juve- behavior, termed “podding” displayed by older nile Lithodes santolla in Steamer Bay (53°36’50’’S; juveniles (Powell & Nickerson, 1965; Dew, 1990; 70°55’45’’W). This bay is a small coastal indentation Lovrich, 1997; Loher & Armstrong, 2000). Pods are on the N shore of the eastern portion of the Strait of social aggregations of individuals of a determined Magellan (Fig. 1). The bay is only 400 m long and age or size, as previously described for lobster species 150 m wide, with an average depth of 5 m. The area (Wahle & Steneck, 1991) and gastropods (Avendaño closest to the coastline consists of a band of rocks et al., 1998) and may help members locate other and boulders, changing with depth to shelly sands. A members of the opposite sex, reduce predation, Macrocystis pyrifera kelp bed occupies the bottom in and increase opportunities for feeding and mating. a band parallel to the coast from depths of 3 to 5 m. During a study describing the ecological recruitment A few plants of Gigartina skottsbergi were scattered cycle of king crab Lithodes santolla on the brown around the area. seaweed Macrocystis pyrifera beds located in a Observations of L. santolla were made during shallow, sandy-rocky embayment (Famine Bay; < 5 the day by SCUBA diving, and photographed using m depth) of the Strait of Magellan, Chile, podding a Nikon Coolpix 995 digital camera in a Sealux CX of L. santolla individuals was discovered around the 995 underwater housing and subtronic strobes. Data holdfasts and stipes/sporophylls of this kelp. In spite were obtained on crab density and sex, the size of the of the economic importance of Lithodes santolla and plants with which the crabs were associated, number a long history of research on the exploited fraction of stipes per plant, and presence of sporophylls of its population, few studies have been done on its (spore-bearing fronds) on the plants. Reconnaissance early benthic stages and population biology (Lovrich, of a large portion of the bay was done to determine 1997), in part due to difficult working conditions in the extent of podding behaviour. Since the patches the field. of M. pyrifera were not homogeneously distributed The formation of pods in crustaceans is a type thoughout the bay, we established six sampling points of behaviour that is occasional, and associated with (one-m2 quadrat) within a total area of about 150 m2 different stages in their life history such as moulting, of the M. pyrifera band, separated from each other mating, and the incubation period. The function of by distances varying between 2 and 30 m. podding in a particular species may vary depending Of the 150 m2 area surveyed, only about 5 on the type of specimens that comprise the pod (e.g. m2 contained important king crab aggregations. maturity stage, sex, intermoult stage) and possible Considerable concentrations of crabs were associated changes in habitat conditions such as water tem- with only a few of the kelp holdfasts in the perature or the presence of predators (Sampedro & reconnaissance area (Fig. 2, Table 1). This table González-Gurriarán, 2004). Previous studies have shows the results from the quadrat used to estimate cited podding in king, tanner, and spider crabs (Dew, the abundance of the juvenile L. santolla associated 1990; Stevens et al., 1992a; Stone et al., 1993; Zhou with the Macrocystis. Plant abundance within the & Shirley, 1997; Sampedro & González-Gurriarán, quadrat ranged from 1 to 5 individuals, with the 2004). Nevertheless, this type of aggregational be- greatest crab abundances occurring where the Podding of juvenile king crabs 107 Figure 1. Location of the study area in Steamer Bay, Strait of Magellan, Chile, visited by diving in August and September 2006. Figura 1. Ubicación del área de estudio en bahía Steamer, estrecho de Magallanes, Chile, donde se desarrolló el buceo en agosto y septiembre de 2006. Table 1. Quantitative data on podding of the subantarctic king crab Lithodes santolla on the kelp Macrocystis pyrifera in Steamer Bay, Strait of Magellan, Chile, in September 2006. Quadrat size = 1 m2. Tabla 1. Antecedentes cuantitativos para describir el proceso de agregaciones en Lithodes santolla sobre el alga parda Macrocystis pyrifera en bahía Steamer, estrecho de Magallanes, Chile, durante septiembre, 2006. Tamaño cuadrantes = 1 m2. Number of Sampling Number of Holdfast diameter Number of king crab/ M. pyrifera plants/ site stipes (cm) quadrat quadrat A 1 5 12 5 B 1 3 15 2 C 2 25, 12 30, 20 54 D 3 4, 6, 4 15, 25, 22 58 E 2 10, 18 30, 32 34 F 5 6, 8, 15, 12, 7 No data 8 plant density was 2 to 3 plants per m2. The highest The greatest crab aggregations occurred in small crab abundances occurred around the plants with areas at depths of less than 3 m, with as many as 60 the greatest number (3-25) of stipes, coinciding crabs hidden in holdfasts covered with sporophylls.
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