Larval development of Maja crispata Risso 1827 (Crustacea,Decapoda, Majidae) reared in the laboratory

The morphology of the zoea and megalop of Maja crispata are described from laboratory-reared material, and compared with other two spider crabs belonging to the subfamily Majinae, Maja squinado and Maja goltziana, recorded in the same region of the eastern Atlantic. The diagnostic characters allowing the separation of these species' larvae are tabulated and discussed.     

The complete larval development of the crab Pilumnus spinifer (Brachyura: Xanthoidea: Pilumnidae) reared in the laboratory

The complete larval development of the crab Pilumnus spinifer from the western Mediterranean was obtained in the laboratory. All four zoeal stages and the megalopa are described and illustrated. The morphological characters of the larvae of Pilumnus spinifer are compared with those of other known larvae of the genus. The zoeae of P. spinifer show the rostral spine longer than the antennule (excluding aesthetascs); short lateral spines present on the carapace, and the mediolateral processes are present only in abdominal somites 2 and 3. The megalopa is similar to that of other Pilumnidae species. The morphology of the larval stages shows very similar characteristics to that of those of P. hirtellus and P. dasypodus, among the described stages of the family.     

Larval development of the circular crab,Atelecyclus rotundatus (Olivi) (Crustacea: Brachyura: Atelecyclidae) reared in the laboratory

The complete larval development is described of laboratory-reared Atelecyclus rotundatus and the stages are compared with larvae of other cancrideans (= corystoideans). The results suggest that the subfamily Atelecyclinae requires reappraising and that present larval evidence does not support the currently accepted grouping of families in the Cancridea.     

The complete larval development of the Mangrove Ocypodid crab Macrophthalmus depressus Ruppell, 1830 (Brachyura: Macrophthalminae) reared in the laboratory

Macrophthalmus depressus larvae were reared in the laboratory using filtered estuarine water of salinity 25±1 ppt and temperature 29–31°C. M. depressus reaches the first crab stage after passing through five zoeal and a megalopa stage requiring 22–23 days. Each stage is described in detail and compared with other known species of the genus.     

Zoeal development of Ethusa microphthalma smith, 1881 (Brachyura,Dorippidae) reared in the laboratory,with a comparison of other dorippid zoeae

The complete zoeal development of a dorippid crab in the subfamily Ethusinae is described for the first time from a known parental female. The ovigerous Ethusa microphthalma was collected in the northern Gulf of Mexico off Louisiana. Larvae passed through four zoeal stages, and the megalopa was reached in 59 days at 20°C and 35 ppt salinity. The larvae differ from those of the few other dorippids for which a zoea is known. Salient distinguishing features include long lateral carapace spines, the presence of six setae on the endopod of the maxillule and maxilla, and a spinose antennal exopod lacking projecting mid-length spines or setae. Zoeal characters are compared to those known for the allied subfamily Dorippinae, and all references to zoeae of the Dorippidae are tabulated.     

The larval and post-larval development of Gibbs's spider crab,Pisa armata (Latreille) [family Majidae: subfamily Pisinae], reared in the laboratory

Summary

The larvae and first crab stage of the spider crab Pisa armata are described from laboratory reared material. The larval stages are compared with previous accounts and with those of Pisa tetraodon. Larval affinities with other genera of Pisinae are discussed.     

Larval development of the fiddler shrimp,Metapenaeopsis stridulans (Alcock, 1905) (Decapoda: Penaeidae) reared in the laboratory

Larvae of Metapenaeopsis stridulans (Alcock, 1905) from Malaysia were successfully reared in the laboratory from the egg to the 1st post-larval stage. The larvae developed through six naupliar, three protozoeal and four mysis stages. The morphology of all these larval stages is described and figured.     

The larval development of Petalomera japonica (Henderson) (Decapoda,Dromiidae) reared in the laboratory

The complete larval development of Petalomera japonica (Henderson) is described, based on laboratory rearing. The species has two zoeal stages and a megalopa. Detailed comparisons are made with other dromiid larvae, particularly those of Petalomera wilsoni.     

Larval development of Pandalus gracilis Stimpson (Crustacea: Decapoda: Pandalidae) reared in the laboratory

The complete larval development of Pandalus gracilis Stimpson is described based on larvae reared in the laboratory. The species has four larval stages (stages 1–4) and one postlarval stage (stage 5). The survival rate of the postlarva stage is very high. Of the 40 larvae reared individually, 39 larvae moulted to the postlarva stage within approximately 21 days at a rearing temperature of 15°C. Larval morphological characteristics of the species are described and figured. Larval development of P. gracilis is compared with other Pandalus and Pandalopsis species. Komai (1999 Komai, T. 1999. A revision of the genus Pandalus (Crustacea: Decapoda: Caridea: Pandalidae).. Journal of Natural History, 33: 1256–1372.  [Google Scholar]) divided species of Pandalus into four species groups based on adult morphology. Pandalus gracilis belongs to the P. hypsinotus group. In this study, using larval characters, the P. hypsinotus group can be divided into two groups by the appearance of the mandibular palp and the shape of the telson: the first group contains P. hypsinotus and P. danae, and the second group contains P. gracilis, P. prensor, and P. nipponensis.     

Larval development of Apiomithrax violaceus (A. Milne Edwards, 1868) (Decapoda: Brachyura: Majoidea: Pisidae) reared in laboratory conditions,and a review of larval characters of Pisidae

Apiomithrax violaceus (A. Milne Edwards, 1868 Milne Edwards A 1868 Observations sur la faune carcinologique des Iles du Cap-Vert Nouvelles Archives du Muséum d'Histoire Naturelle, 4, 49–68, pls 16–18  [Google Scholar]) is a pisid majoid crab occurring in tropical and subtropical coastal waters of the eastern and western South Atlantic. Larval development consists of two zoeal stages and a megalopa. Beginning with the first zoea, the duration of each larval stage at 24°C was 3–8 (5±1), 3–5 (4±0.5) and 9–15 (11±2) days, the megalopa and first crab instar appearing 9–11 (10±1) and 20–27 (23±2) days after hatching, respectively. Larval characters agree with those proposed for the Majoidea, in having nine or more setae on the scaphognathite in the first zoea and well-developed pleopods in the second zoea. However, larvae of A. violaceus do not fit larval pisid features. Zoeal stages differ from most other Pisidae in having lateral spines, a long rostral spine extending beyond the antenna, two spines per telson fork and a dorsolateral process on the third abdominal somite. The megalopa differs in having a spine dorsally on the carapace and on the basial segment of the second pereiopod. Two characters that are potentially unique to Apiomithrax include a zoeal antenna with an exopod that is much longer than the protopod, and a rostral spine that is longer than the dorsal spine. These characters should facilitate the identification of this taxon and could also be useful for phylogenetic studies. A review of larvae of 28 species among 14 genera indicated that there is no apparent single larval character that differentiates the Pisidae, with more limited phylogenetic analyses suggesting that this is a paraphyletic group. Apiomithrax, Eurynolambrus, Pisoides, Rochinia and Scyra have the most divergent morphological characters within the family. The analysis and inclusion of additional taxa is likely to shed more light on the sister-group relationships of the Pisidae. However, based on the extent of morphological interspecific variability of known larvae it is likely that the group, as presently defined by adult morphology, is not monophyletic.     

Re-establishment of the Family Eumedonidae Dana, 1853 (Crustacea: Brachyura)

On the basis of a re-examination of all available data concerning the systematic position and status of the genus Eumedonus and allied genera it is concluded that these taxa form a separate family within the superfamily Xanthoidea (sensu Guinot, 1978). The family is characterized not only by particular morphological features but by the symbiotic mode of life of its members.     

Complete larval development of the rare porcellanid crab,Novorostrum decorocrus Osawa, 1998 (Crustacea: Decapoda: Anomura: Porcellanidae), reared under laboratory conditions

The complete larval development of Novorostrum decorocrus Osawa, , is described and illustrated on the basis of laboratory‐reared material. Two zoeal stages and one megalop stage were recorded. Zoeas of N. decorocrus closely resemble those of N. indicum in the appendage characters, including the endopod of the maxillule with only a single stout seta on the distal margin. This character is unique to Novorostrum zoeas. However, N. decorocrus is distinguished from N. indicum by the setation on the endopod of the maxilla and the basis of the second maxilliped in both zoeal stages. The megalops of N. decorocrus are characterized by having a strongly elongate carapace, and differs considerably from the adults in the structure of the carapace, rostrum and third thoracic sternite, and in the armature of the pereiopods. The larval duration of N. decorocrus suggests that this rare porcellanid is more widely distributed than currently known.     

The occurrence,mechanics and significance of burying behaviour in crabs (Crustacea: Brachyura)

Although the terms burrowing and burying are often used interchangeably in the literature, there are clear distinctions between these two types of behaviour in terms of their ecological, mechanical and physiological implications. Both types of behaviour are widely observed in the Brachyura. In comparison to the well researched area of burrowing in crabs, information on burying is relatively dispersed. This review will examine the extent of burying behaviour in brachyurans, and the physiological and ecological consequences of the behaviour within the group. At least nine of the 50 families of brachyuran crabs have either been observed to bury in soft substrata or are suspected, on morphological grounds, of burying. There appears to be no specific morphological adaptations for burying in brachyurans, apart from those features associated with respiration whilst buried in the sediment. Buried individuals must ensure constant access to oxygenated water in the face of mechanical problems resulting from direct contact with the sediment, i.e., the threat of clogging. Burying taxa deal with this challenge through accessory respiratory channels and altered respiratory rhythms. The evolutionary implication of the burying habit is equivocal. Burying taxa are amongst the most speciose and numerically dominant brachyuran groups in marine systems, all reaching their greatest diversity and abundance in soft substrata. Burying may be an ancestral condition, with many of these groups evolving in habitats characterized by soft sediment.     

The larval development of the mud shrimp Upogebia yokoyai Makarov, 1938 (Decapoda: Gebiidea: Upogebiidae) reared under laboratory conditions

Larval development of the mud shrimp Upogebia yokoyai Makarov, 1938 Makarov, VV. 1938. Crustacea Anomura. Fauna USSR. 10;3, Moscow, Leningrad: AN SSSR.  [Google Scholar] (Decapoda: Gebiidea: Upogebiidae) is described and illustrated for the first time from material reared in the laboratory. The development includes four zoeal stages and a megalopa. At 20–22°C the megalopa was attained 16 days after hatching. The zoeae of U. yokoyai are distinguishable from those of the sympatric species Upogebia major and Upogebia issaeffi, inhabiting Russian waters of the Sea of Japan, by the presence of two pairs of spines (posterolateral and posterodorsal), each on the fourth and fifth pleonal somites. The megalopa of U. yokoyai differs in the length of the rostral spine, shape of telson and number of antennular aesthetascs.