Siboga expeditie.

Mono.39c (Decapoda Brachyura: Hymenosomidae, Retroplumidae, Ocypodidae, Grapsidae, Gecarcini); L.82

Siboga expeditie.

Mono.39a (Decapoda: Penaeidae); Livr.55

Siboga expeditie.

Mono.39b[1] (Decapoda Brachyura: Oxystomata, Dorrippidae); Livr.78

Siboga expeditie.

Mono.39b (Decapoda: Dromiacea); Livr.71

Siboga expeditie.

Mono.39aSupp (Decapoda: Penaeidae); Livr.69

Siboga expeditie.

Mono.39a[1] (Decapoda: Alpheidae); Livr.60

Siboga expeditie.

Mono.39b[2] (Decapoda Brachyura: Oxystomata: Calappidae, Leucosiidae, Raninidae); Livr.85

Siboga expeditie.

Mono.39c[1] (Decapoda Brachyura: Goneplacidae and Pinnotheridae); Livr.84

Siboga expeditie.

Mono.39a[2] (Decapoda: Eryonidae, Palinuridae, Scyllaridae, and Nephropsidae); Livr.76

Siboga expeditie.

Mono.39a[4] (Decapoda: Macrurous Decapod Crustacea, Penaeidae and Alpheidae); Livr.93

Siboga expeditie.

Mono.39[a]3 (Decapoda: Pasiphaeidae, Stylodactylidae, Hoplophoridae, etc.); Livr.87

Molt cycle of the natural population of Palaemonetes argentinus (Crustacea, Palaemonidae) from Los Padres Lagoon (Buenos Aires, Argentina)

The molt cycle of the natural population of Palaemonetes argentinus Nobili, 1901 from Los Padres Lagoon, Buenos Aires, Argentina, was studied in relation to age, sex, and environmental factors. A total of 1645 individuals (740 females, 539 males, and 366 juveniles) were collected and analyzed between December 1995 and December 1996. The results indicate that the sex ratio (males:females) remains around 1:1.4 throughout most of the year. The reproductive period extends from September until February (spring and summer), with maximum sexual activity in October and November. Two cohorts originated in the spring and in the summer were differentiated. Ovigerous females arrest their molt cycle during the intermolt period to restart it after oviposition. The duration of the intermolt period does not differ between adults and juveniles. Since the percentage of premolt individuals represents 60% of the total cycle, it was classified as a diecdysic cycle. Within the studied range of water temperatures, the observed variations in the span of the different stages, indicate that this factor does not alter the molt frequency. Like in the rest of decapods, the intermolt duration of P. argentinus is modified by ovarian maturation.

Crustáceos no cerrito Ariano Souza, Rio Grande, Rio Grande do Sul e distribuição de Callinectes sapidus (Brachyura, Portunidae)

While all species of the genus Callinectes Stimpson, 1860 have a continuous distribution on the Atlantic coast of the Americas, Callinectes sapidus Rathbun, 1896 is the only one with disjunct distribution. Considering that this species was introduced in Europe and Japan, it has been suggested that the occurrence of C. sapidus on the southern coast of Brazil was due to the transport by ballast water. In the archaeological site Ariano Souza, located in the estuary of the Patos Lagoon (southern Brazil), remains of crustaceans, including claws of approximately two thousand years ago, were found. A preliminary analysis of this material showed Callinectes chelae. Because this archaeological site is located inside the estuary, it has been hypothesized that these chelae belong either to C. sapidus or to C. danae Smith, 1869. A comparison between pincers collected in the archaeological and pincers of these two species (90 dactyls, 30 of each type) was performed. The analysis (ANOVA) considered the variability of seven characters of the dactyls, and demonstrated the existence of two groups. Results showed that the measured characters suffice to separate these species, and indicated that the material found in the archaeological site belongs to C. sapidus. The hypothesis of the introduction of C. sapidus in the area is rejected. The possible biogeographic history of the species is discussed.

Spatial and temporal distribution of decapod larvae in the subtropical waters of the Arvoredo archipelago, SC, Brazil

The present paper aims to describe the temporal and spatial distribution of the composition and abundance of Decapoda larvae in the shallow waters around Arvoredo Marine Biological Reserve. Stomatopod occurrence is also discussed. Plankton samples were collected at five sites around the Arvoredo Island every two months for one year from May, 2002 to April, 2003. Thirty-nine morphotypes, 11 genus and 4 species (Artemesia longinaris Bate, 1888, Hexapanopeus schmitii Rathbun, 1930, Menippe nodifrons Stimpson, 1859 and Pleoticus muelleri Bate, 1888) were identified, among them only two morphotypes of Stomatopoda larvae, and the remainder Decapoda larvae. Brachyuran zoeae were the most abundant group and they were well represented by Portunidae and Xanthidae zoeae. Lucifer sp. and Caridea zoeae were the most abundant non-brachyuran taxa. Decapod larvae were observed to occur at all sampling sites, however the spatial distribution demonstrated a general tendency to greater abundance and diversity at the southern sites of the Island. Decapoda and Stomatopoda larvae occurred throughout the year, showing that reproduction is continuous, but that larval input in planktonic community was significantly higher during autumn and spring.

Dieta de juvenis de Trachinotus carolinus (Actinopterygii, Carangidae) em praias arenosas na costa do Rio de Janeiro

Estudamos a dieta dos juvenis de Trachinotus carolinus (Linnaeus, 1766) em praias da Baía de Sepetiba (Rio de Janeiro, Brasil) entre janeiro de 2000 e abril de 2001. Procuramos avaliar a plasticidade trófica de peixes desta espécie ao longo de um gradiente espacial com diferentes níveis de exposição às ondas, sazonalidade, além de avaliar mudanças ontogenéticas na dieta. Os itens alimentares foram analisados através do índice de importância relativa (IIR), determinado pelos valores das frequências de ocorrência, de número e de peso. Os itens de maior importância foram do subfilo Crustacea, ordens Mysidacea, e o representante da ordem Decapoda Emerita brasiliensis (Schmitt, 1935), além de Cefalochordata, representado por Branchiostoma platae (Fitzinger, 1862). Na zona de maior exposição às ondas (praia de Barra de Guaratiba) e com substrato predominantemente arenoso, a dieta foi constituída principalmente por Emerita brasiliensis e Cirripedia, este último presente nos costões rochosos que limitam a praia; na zona de exposição intermediária (praia de Muriqui), houve um predomínio de Mysidacea e Branchiostoma platae; na zona mais protegida (praia de Itacuruçá), os itens de maior abundância foram Polychaeta, Mysidacea e Branchiostoma platae. Sazonalmente não ocorreu variação no uso de Mysidacea, enquanto Branchiostoma platae foi mais consumido durante o inverno, Polychaeta na primavera e Cirripedia e Emerita brasiliensis, no verão. Mysidacea foi o alimento predominante em todas as classes de tamanho, enquanto Polychaeta foi utilizado predominantemente por peixes menores que 20 mm de comprimento padrão e Emerita brasiliensis e Cirripedia foram consumidos principalmente por indivíduos maiores que 40 mm, somente na praia de maior exposição. O sucesso no uso de praias desprotegidas e zonas de arrebentação por esta espécie de peixe pode ser em parte devido à estratégia trófica oportunista, que utiliza uma ampla variedade de recursos disponíveis no ambiente.