The zoeal development of Platymaia wyvillethomsoni Miers, 1886 (Crustacea: Decapoda: Majoidea: Inachidae) described from laboratory reared material

The spider crab Platymaia wyvillethomsoni was reared in the laboratory, from hatching to the megalopal stage at 20°C. The larval development comprises two zoeal stages and a megalopa. The zoeal stages are described for the first time and compared with those of the four known species of the family Inachidae from the northern Pacific. The zoeal characters (carapace spines, antenna, mouthpart appendages, pleon and telson fork) of P. wyvillethomsoni are significantly different from those of two Achaeus species from northern Pacific and other inachid genera (Inachus and Macropodia) from the Atlantic. Therefore, this species should not be placed in the family Inachidae based on zoeal morphology. A provisional key for the identification of known zoeae of the family from the northern Pacific is provided.     

The early phyllosoma stages of spiny lobster Panulirus echinatus Smith, 1869 (Decapoda: Palinuridae) reared in the laboratory.

The early stages of the Panulirus echinatus were hatched and reared in the laboratory. Ovigerous females were captured in their habitat and carefully transported to the laboratory. Larvae were transferred in a recirculation water tank at a density of 10 larvae.L(-1). The larvae were fed on Artemia and gonads of mussel Brachydonts sp. Microalgae Dunaliella viridis was added at a concentration of 150 x 10(4) cell.mL(-1). Larvae and exuviae of each zoeal stage were preserved in an alcohol 70% + glycerin (1:1) solution. The phyllosomas moulted eight times; the intermoulting period of each instar averaged about 7 to 10 days. The main morphological changes of each appendage were described in detail, illustrated and compared with previous reports.     

Larval stages of Brachynotus atlanticus Forest, 1957 (Crustacea: Decapoda: Grapsidae) reared under laboratory conditions

The complete larval development of the Eastern Atlantic grapsidcrab, Brachynotus atlanticus, was obtained in the laboratory.Five zoeal stages, the megalopa and the first crab stage aredescribed and illustrated. Under laboratory conditions at 23°Cthe first crab appeared on the 25th day. This is the first speciesof the genus for which the complete larval development is known.Larval features are compared with those of other members ofthe subfamily Varuninae.     

Larval development of Crangon hakodatei Rathbun (Decapoda: Crangonidae) reared in the laboratory

Complete larval development of Crangon hakodatei Rathbun isdescribed, based on material hatched in the laboratory fromovigerous females. The species has six zoeal stages and onepostlarval stage. The morphological characters of the larvaland postlarval stages are described with illustrative figuresand compared with those of two congeneric species. The zoealstages of C. hakodatei can be distinguished from those of otherCrangon species in the number of segments of the antennule peduncle,the number of setae on the antennal scale and basis of the maxillipeds,and the stages of appearance of pereiopods. The first zoealstage in the seven species of Crangon are compared and an annotatedkey for distinguishing them is also provided.     

Facultative secondary lecithotrophy in the megalopa of the shrimp Lysmata seticaudata (Risso, 1816) (Decapoda: Hippolytidae) under laboratory conditions

Certain decapod crustaceans can catabolize internal reservesto undergo partial or full larval development. This featureis termed secondary lecithotrophy, if energy used results fromplankton derived organic matter accumulated by earlier larvalstages. The present work reports the ability of Lysmata seticaudatamegalopa to molt to the first juvenile stage in the absenceof food. Unlike previous records of secondary lecithotrophydisplayed by non-feeding last larval stages of hermit crabsand spiny lobsters, the megalopa of L. seticaudata retains itsfeeding capacity. This is the first time such a feature hasbeen reported in decapods, and the term facultative secondarylecithotrophy is proposed. The build up of energy reserves continuesduring the last zoeal stage of L. seticaudata, with starvedzoea IX failing to molt to megalopa. Energy reserves that enablestarved megalopa to molt to juvenile seem to be partially depleted,with starved juveniles produced either from starved or fed megalopaebeing unable to molt to the next juvenile stage. The longerresistance of starved juveniles produced from fed megalopae(nine days), compared to that of starved juveniles producedfrom starved megalopae (five days), indicates that some energyreserves may pass to the juvenile, not being totally depletedat metamorphosis.     

The larval development of Penaeus semisulcatus de Haan, 1850 (Decapoda, Penaeidae) reared in the laboratory

P. semisulcatus is a commercially important species of the ArabianSea. In the present studies the mature females were broughtfrom the sea to the laboratory for spawning. The spawned eggswere reared in laboratory conditions up to the post larval stage.Five naupliar, three protozoeal, three mysis and first postlarval stages were described. The diagrams were made with thehelp of camera lucida. The measurements were made with a micrometer.     

Growth patterns,chemical composition and oxygen consumption in early juvenileHyas araneus (Decapoda: Majidae) reared in the laboratory

Early (instar I and II) juveniles of the spider crabHyas araneus were reared under constant conditions (12 °C, 32‰S) in the laboratory, and their growth, biochemical composition, and respiration were studied. Every second day, dry weight (W), ash-free dry weight (AFW), and contents of ash, organic and inorganic carbon (C), nitrogen (N), hydrogen (H), protein, chitin, lipid, and carbohydrates were measured, as well as oxygen consumption. Changes in the absolute amounts of W. AFW, and C, N, and H during the moulting cycle are described with various regression equations as functions of age within a given instar. These patterns of growth differ in part from those that have been observed during previous studies in larval stages of the same and some other decapod species, possibly indicating different growth strategies in larvae and juveniles. There were clear periodic changes in ash (% of W) and inorganic C (as % of total C), with initially very low and then steeply increasing values in postmoult, a maximum in intermoult, and decreasing figures during the premoult phase of each moulting cycle. Similar patterns were observed in the chitin fraction, reaching a maximum of 16% of W (31% of AFW). Ash, inorganic C, and chitin represent the major components of the exoskeleton and hence, changes in their amounts are associated with the formation and loss of cuticle material. Consequently, a high percentage of mineral matter was lost with the exuvia (76% of the late premoult [LPM] ash content, 74% of inorganic C), but relatively small fractions of LPM organic matter (15% of AFW, 11% of organic C, 5–6% of N and H). These cyclic changes in the cuticle caused an inverse pattern of variation in the percentage values (% of W) of AFW, organic C, N, H, and biochemical constituents other than chitin. When these measures of living biomass were related to, exclusively, the organic body fraction (AFM), much less variation was found during individual moulting cycles, with values of about 43–52% in organic C, 9–10% in N, 6–9% H, 31–49% of AFW in protein, 3–10% in lipid, and <1% in carbohydrates. All these constituents showed, on the average, a decreasing tendency during the first two crab instars, whereas N remained fairly constant. It cannot be explained at present, what other elements and biochemical compounds, respectively, might replace these decreasing components of AFW. Decreasing tendencies during juvenile growth were observed also in the organic C/N and in the lipid/protein weight ratios, both indicating that the proportion of lipid decreased at a higher rate than that of protein. Changes were observed also in the composition of inorganic matter, with significantly lower inorganic C in early postmoult (2–4% of ash) than in later stages of the moult cycle (about 9%). This reflected probably an increase in the degree of calcification, i.e. in the calcium carbonate content of the exoskeleton. As a fraction of total C, inorganic C reached maximum values of 17 and 20% in the crab I and II instars, respectively. The energy content of juvenile spider crabs was estimated independently from organic C and biochemical constituents, with a significant correlation between these values. However, the former estimates of energy were, on the average, significantly lower than the latter (slope of the regression ≠1). Since organic C should be a reliable integrator of organic substances, but the sum of protein, lipid, chitin, and carbohydrates amounted to only 60–91% of AFW, it is concluded that the observed discrepancy between these two estimates of energy was caused by energy from biochemical constituents that had not been determined in our analyses. Thus, energy values obtained from these biochemical fractions alone may underestimate the actual amount of organic matter and energy. Respiration per individual in juvenile spider crabs was higher than that in larval stages of the same species (previous studies), but their W-specific values of oxygen consumption (QO₂) were lower than in conspecific larvae (0.6–2μg O₂·[mg W]⁻¹). QO₂ showed a consistent periodic pattern in relation to the moult cycle: maximum values in early postmoult, followed by a rapid decrease, and constant values in the intermoult and premoult phases. This variation is interpreted as an effect mainly of cyclic changes in the amounts of cuticle materials which are metabolically inactive. From growth and respiration values (both expressed in units of organic C), net growth efficiency, K₂, values may be calculated. In contrast to previous findings in larval stages, K₂ showed an increasing trend during growth of the first two juvenile instars ofH. araneus.     

The larvae of the spider crab Pisoides bidentatus (A. Milne-Edwards, 1873) (Decapoda: Majoidea: Pisidae) reared under laboratory conditions

Larval development of the spider crab, Pisoides bidentatus (A.Milne-Edwards, 1873) (Decapoda: Majoidea: Pisidae), inhabitingthe Russian waters of the Sea of Japan is described and illustratedfor the first time from larvae reared in the laboratory. Thedevelopment included two zoea and one megalopa, thus followingthe typical pattern in the Majoidea. At a temperature of 20–22°Clarval development of P. bidentatus took from 9 to 13 days.The comparative analysis revealed that the larvae of two Pisoidesspecies differ in numerous characters whereas zoea of P. bidentatusand Pugettia quadridens belonging to different families arenearly identical. According the larval characters, P. bidentatusand P. quadridens should be assigned to one genus. The larvaldata lend the support to revision the taxonomic position ofP. bidentatus.     

Larval,megalopal and early juvenile development in Pagurus granosimanus (Stimpson, 1859) (Decapoda: Anomura: Paguridae) reared in the laboratory

Summary

The larval, megalopal and early juvenile stages of Pagurus granosimanus are described, illustrated and compared with other North Pacific species of the genus. Morphologically, the zoeae of P. granosimanus appear most similar to the Japanese P. brachiomastus in the majority of characters, but share the endopodal setation of the third maxilliped with a second Japanese species, P. pectinatus. The megalopae of P. granosimanus are unlike those of other North Pacific species in having 5+5 marginal setae on the telson, rather than the customary 4+4, or less frequent 3+3. Comparison of juvenile characters is limited to pleopodal changes among the regional species for which data are available. P. granosimanus is unusual in undergoing complete pleopodal loss at the second crab stage with return of left pleopods in the fourth stage.     

Correct diagnosis of early zoeal stages of Athanas nitescens (Leach, 1814) (Decapoda, Caridea, Alpheidae) using laboratory-raised larvae

The morphology of the first two larval stages of Athanas nitescens(Leach, 1814), reared under laboratory conditions, is redescribed.The present data are compared with previous works, since a clarificationof the morphological characters of the first two larval stagesof A. nitescens is needed, in order to avoid misidentificationof these stages in the future.