Breeding and larval distribution of the pteropod Clione limacina in the North Atlantic,Subarctic and North Pacific Oceans

The pteropod Clione limacina (Phipps, 1774) is an arcticboreal, circumpolar species, which is widely distributed in the North Atlantic and Subarctic Oceans; it also occurs in the North Pacific Ocean (in the Oyashio and neighbouring waters) and along the Atlantic coast of North America in the waters of the cold Labrador current to the Cape Hatteras region (35° N). The distribution of C. limacina larvae in the plankton of the Norwegian, Barents and White Seas, the Bear Island-Spitsbergen region of the Greenland Sea, the Newfoundland Grand Bank and the Flemish-Cap Bank region of the North-western Atlantic Ocean, and the Kurile-Kamchatka region of the North-western Pacific Ocean has been studied, and information from literature concerning the reproduction and larval occurrence of the species is summarized. Throughout its distributional are, spawning of C. limacina is characterized by the same general ecological pattern. This species breeds and spawns in all types of water masses occurring within the vertical range which it commonly inhabits — from surface layers to 500 m water depth. In all local populations of the species, the most intensive spawning is correlated with the spring/summer period of annual heating of the local waters, and the highest abundance parallels maximum growth of phytoplankton which serves as food for veligers and early polytrochous larvae. After the end of this period, spawning intensity in all local C. limacina populations declines sharply, but spawning continues at low intensity during the autumn/winter season, being practically continuous throughout the year. Distribution patterns of C. limacina larvae are determined by those of their parental forms (the parental forms spawn in the zones permanently inhabited). The earliest larval stages of C. limacina (veligers) are present predominantly in the upper 100 or 200 m water layer, i.e. in the zone of high phytoplankton abundance. Polytrochous larvae, after becoming predaceous feeders, are distributed throughout the whole water column from the surface to 500 m depth, similar to adult C. limacina. As with the adults, larvae are present (within the species' distribution area) in all types of water masses. Since the beginning of the twentieth century, in the course of the warming of the Arctic Ocean, the southern race of C. limacina (formerly a summer/autumn seasonal invader in the Norwegian Sea) has become a permanent component of the plankton fauna of the Norwegian and Barents Seas in regions influenced by the Norwegian-Northcape Current System.     

Organogenesis and histogenesis in the planktotrophic veliger of Doridella steinbergae (Opisthobranchia: Nudibranchia)

Development of the planktotrophic veliger of the dorid nudibranch Doridella steinbergae (Lance) was studied by histological examination of 4, arbitrarily defined larval stages. Following an embryonic period of 7 1/2 to 8 days (12° to 15°C), the newly hatched veligers possess a functional digestive tract, a pair of nephrocysts, a secondary kidney, a pair of cerebral ganglia, a larval shell consisting of a two-thirds whorl, and the metapodial component of the foot. Development during Stage I mainly involves growth of the larval shell and the visceral organs. Stage II is marked by the retraction of the mantle fold from the shell aperture and the appearance of the eyespots, gonadal rudiment, larval heart, and the optic, pedal, and pleural ganglia. At Stage III the radular sac rudiment evaginates from the esophageal wall, the buccal ganglia differentiate, and the propodial rudiment begins to develop on the ventral surface of the metapodium. Stage IV veligers, which are competent to metamorphose, possess 6 pairs of radular teeth, lipid deposits in the left digestive gland, rudiments of the adult kidney and the oral lip glands, an hypertrophied mantle fold, a propodium, and densely packed cilia over the entire ventral surface of the foot. The length of the obligatory larval period, from hatching of the veliger until the attainment of metamorphic competence, is 25 to 26 days under laboratory culture conditions and the larval shell grows from 142 to 168 m in length. The sequence of morphogenetic events and the structure of the competent veliger of D. steinbergae is compared to that of other opisthobranch veligers. It is suggested that the relatively small maximal shell size attained by D. steinbergae results from precocious retraction of the mantle fold. It is further suggested that interspecific differences in the kinds of structures that develop during the veliger phase of opisthobranchs may relate to variations in the requirements of the juvenile phase. The functional adaptations of the gut of planktotrophic veligers are discussed and compared to those of lecithotrophic veligers.     

Development and metamorphosis of the planktotrophic larvae of Rostanga pulchra (Mollusca: Nudibranchia)

Rostanga pulchra MacFarland, a small (1 to 2 cm) dorid nudibranch, lays an average of 7000 eggs in the laboratory during a period of 30 days in the summer. The veligers hatch 15 to 16 days after oviposition and it takes another 35 to 40 days to become competent for metamorphosis at a temperature of 10° to 15°C. Larval cultures were maintained initially at a concentration of 500 veligers per 100 ml of filtered sea water (antibiotics added). During the planktotrophic phase of development, the veliger grows from 150 to 300 m in shell length. Although the veligers are generalists in their food preference, the best result (faster growth) was achieved by feeding them with a combination of Monochrysis lutheri and Isochrysis galbana. The concentration of food cells was kept at 10⁴ cells per ml of culture media and was supplied every 2 to 3 days. A veliger which is competent to metamorphose is identifiable morphologically by its propodium, eyespots, rhinophores, and spiculated dorsal papillae. The entire metamorphic process lasts 24 h when a suitable substrate such as the food sponge Ophlitaspongia pennata is provided. The competent veliger is able to delay metamorphosis for at least 3 weeks. Juveniles were kept in the laboratory for 70 days and, during this period, grew to a length of 4.5 mm.     

Effects of various temperature cycles on the larval development of the gastropod molluscCrepidula fornicata

Veligers ofCrepidula fornicata (L.) were reared for 12 days at constant temperatures of 15°, 20°, 25°, 30° and 35°C, and at 5 C° daily cycles of equal periodicity (COEP) over the temperature ranges 15° to 20°C, 20° to 25°C, 25° to 30°C and 30° to 35°C. COEP consisted of equal periods (6 h) of maximum temperature, minimum temperature, and uniformly increasing and decreasing temperature each 24 h period. Survival was high and not influenced by cyclic or constant temperature from 15° to 30°C. At 35°C and COEP 30° to 35°C, all larvae died before Day 6. Shell growth rate increased markedly over the range 15° to 25°C, and growth rates at cyclic temperatures in this range were intermediate between growth rates at the corresponding constant temperatures. Larvae reared at COEP 15° to 20°C and COEP 30° to 35°C had discontinuities in their shells due to inhibition of shell secretion during the adverse part of each temperature cycle. Groups ofc. fornicata veligers were exposed for 2 days to daily temperature cycles of equal and unequal periodicity in the critical 30° to 35°C range. [Cycles of unequal periodicity (COUP) consisted of unequal periods (varying between 3 and 15 h) of maximum and minimum temperature and uniformly increasing and decreasing temperature each 24 h period.] These veligers showed shell growth although their body tissue declined, as indicated by decreasing carbon content per larva. Least shell growth and most body tissue loss occurred in those cycles with the longest exposure to higher temperature. Larvae exposed for arious days to the mildest 30° to 35°C COUP (15 h at 30°C, 3 h increasing temperature, 3 h at 35°C and 3 h decreasing temperature) recovered and resumed normal growth when transferred to constant 30°C, but their growth was retarded in proportion to the number of days in the temperature cycle. Rates of shell growth of veligers in temperature cycles show an immediate effect of environmental temperature, while changes in carbon content per larva better reflect the effects of temperature on general metabolism and survival.     

Isolation of DNA and RNA from ascidians

Combined effects of temperature, salinity and nutrition on larval survival and growth of the European oyster Ostrea edulis L. were studied over a period of seven days in the laboratory. Larvae were obtained in August 1985 from oysters reared under field conditions on the Mediterranean coast. Four temperatures (15°, 20°, 25°, 30°C), four salinities (20, 25, 30, 35 S) and two levels of nutrition (fed or unfed) were used in the experimental design; the fed larvae received a mixed algal diet of Isochrysis galbana and Chaetoceros calcitrans forma pumilum at a concentration of 100 cells per microlitre. Larvae survived over a wide range of temperature and salinity; statistical analysis indicated that nutrition had the greatest effect on the development of O. edulis larvae, explaining 85 to 88% of the variance in growth. Compared with temperature, the effect of salinity was very slight, usually statistically insignificant. The combined effects of temperature and nutrition produced the only significant interaction. Growth of starved larvae seems to be independent of both temperature and salinity within the range of levels tested.     

Embryogenesis and larval biology of the ahermatypic scleractinian<Emphasis Type="Italic"> Oculina varicosa</Emphasis>

The ivory tree coral Oculina varicosa (Leseur, 1820) is an ahermatypic branching scleractinian that colonizes limestone ledges at depths of 6–100 m along the Atlantic coast of Florida. This paper describes the development of embryos and larvae from shallow-water O. varicosa, collected at 6–8 m depth in July 1999 off Fort Pierce, Florida (27°32.542 N; 79°58.732 W). The effect of temperature on embryogenesis, larval survival, and larval swimming speed were examined in the laboratory. Ontogenetic changes in geotaxis and phototaxis were also investigated. Embryos developed via spiral cleavage from small (100 µm), negatively buoyant eggs. Ciliated larvae developed after 6–9 h at 25°C. Embryogenesis ceased at 10°C, was inhibited at 17°C, and progressed normally at 25°C and 30°C. Larval survival, however, was high across the full range of experimental temperatures (11–31°C), although mortality increased in the warmest treatments (26°C and 31°C). Larval swimming speed was highest at 25°C, and lower at the temperature extremes (5°C and 35°C). An ontogenetic change in geotaxis was observed; newly ciliated larvae swam to the water surface and remained there for approximately 18 h, after which they swam briefly throughout the water column, then became demersal. Early larvae showed no response to light stimulation, but at 14 and 23 days larvae appeared to exhibit negatively phototactic behavior. Although low temperatures inhibited the development of O. varicosa embryos, the larvae survived temperature extremes for extended periods of time. Ontogenetic changes in larval behavior may ensure that competent larvae are close to the benthos to facilitate settlement. Previous experiments on survival, swimming speeds, and observations on behavior of O. varicosa larvae from deep-water adults indicate that there is no difference between larvae of the deep and shallow populations.Communicated by J.P. Grassle, New Brunswick     

Laboratory study of survival and duration of individual zoeal stages as a function of temperature in the brachyuran crab Cancer magister

Larvae were hatched from ovigerous Dungeness crabs, Cancer magister, collected from Puget Sound Basin, Washington, USA, in April, 1986, and the effects of temperature on rates of survival and development were studied for each of the five zoeal stages both in small batch-culture and in individual culture. Culture method had little effect on the results at 10°, 15°, and 20°C. Increased mortality was measured at all stages at 20°C, with 100% mortality occurring during the terminal fifth stage. Fifth stage larvae may also show higher mortality at 15°C than at 10°C. Stage duration varied inversely with temperature at all stages, although differences between 10° and 15°C were greater than between 15° and 20°C. The results indicate that survival and stage duration are independent of the values for the previous and subsequent stages, that variability among larvae in instar duration increases with temperature, and that the terminal fifth zoeal stage is the most sensitive to temperature stress. Duration of a late zoeal instar is not related to its earlier development rate nor can early development rates be used to predict whether individual zoeae will successfully develop to the megalopa. Measurements of megalopa dry weights indicate no differences due either to previous culture temperatures or to total time to the megalopa. Predictive models of larval transport that require estimates of larval duration should account for both changes in temperature response that can affect individual stage duration, and variability among individuals in stage duration that can influence the degree of larval dispersion.     

Growth rate of the bathypelagic crustacean Gnathophausia ingens (Mysidacea: Lophogastridae). I. Dimensional growth and population structure

Gnathophausia ingens has 13 instars, each with a distinct range of sizes which does not overlap the sizes of adjacent instars. The intermolt interval, measured in the laboratory at 5.5°, 6.5° and 7.5°C, increases with increasing size and decreases with increasing temperature. At 5.5°C it varies from 166 days for the smallest individuals to 253 days for the oldest. The period of larval development in the marsupium of a female is estimated to be 530 days. The life span of females is estimated to be 2,950 days with the onset of reproduction at 2,400 days. It is sugquested that this species is semelparous. The population structure data suggest that there is low mortality through the first 7 instars, progressively higher mortality from Instar 8 through Instar 11, and slightly lower mortality in the remaining 2 instars. These life-history characteristics appear to be directed toward maximizing absolute fecundity (as opposed to time-specific fecundity) in a stable environment. These characteristics may have been selected for by low available food energy and made possible by the stability of the deep sea.     

Synergistic effects of cadmium and salinity combined with constant and cycling temperatures on the larval development of two estuarine crab species

The developmental stages from megalopa to third crab of the blue crab Callinectes sapidus Rathbun were tested in 12 combinations of cadmium (0, 50, and 150 ppb) and salinity (10, 20, 30, and 40) at 25°C. A reduction in survival and a significant delay in development from megalopa to third crab occurred within each salinity regime in 50 ppb compared with the control. Comparison of the delay in development within each salinity regime revealed that the sublethal effect of cadmium was most pronounced in the salinities normally preferred by C. sapidus. A similar comparison within each cadmium concentration, however, showed that the developmental time from megalopa to third crab was approximately the same irrespective of salinity. The developmental stages from hatch to first crab of the mud-crab Rhithropanopeus harrisii (Gould) were examined in 63 combinations of cadmium (0, 50, and 150 ppb), salinity (10, 20, and 30), constant temperature (20°, 25°, 30°, and 35°C) and cycling temperature (20° to 25°C, 25° to 30°C, and 30° to 35°C). The results indicated that cycling temperatures may have a stimulating effect on survival of the larvae compared to constant temperatures, both in the presence and in the absence of cadmium. Effects of cadmium and salinity and their interaction on the survival of the larvae from zoeae to megalopa were documented at most of the temperatures by analyses of variance. The zoeal larvae were more susceptible to cadmium than the megalopa. Effects of different combinations of cadmium and salinity on the duration of larval development were assessed by a t-test.     

The response of sea scallop (Placopecten magellanicus) veligers to a weak thermocline in 9-m deep mesocosms

We examined the vertical distributions of scallop (Placopecten magellanicus) veligers in deep (0.6 m diameter, 9.5 m deep) polyethylene mesocosms from December 1991 to January 1992. In the mesocosms temperature stratification varied from 0 to 1.5 °C. Profiles of vertical distribution revealed several repeated patterns. Peaks in veliger numbers often appeared at the water surface and just above the thermocline. Higher density patches were seen below the surface peaks, and revealed the presence of bio-convective cells. Distribution away from these discontinuities was usually even. Distribution of veligers was affected by thermoclines above 1.0 °C. Responses to thermoclines varied with larval age and time of day, and 28 to 30 d veligers passed in both directions through a 1.5 °C thermocline. We conclude that larval behaviour is a major determinant of whether veligers pass through a thermocline. Kinematic viscosity may play a role in perception of temperature changes. Two potential consequences of such behaviour are (1) remaining in more productive upper water layers, where feeding opportunities are enhanced, and (2) increased horizontal transport in the region of the thermocline, which may enhance recruitment. Received: 15 May 1996 / Accepted: 11 May 2000     

Effect of temperature on the egg and yolk-sac larval development of common pandora,<Emphasis Type="Italic"> Pagellus erythrinus</Emphasis>

Temperature is one of the most critical environmental factors for fish ontogeny, affecting the developmental rate, survival and phenotypic plasticity in both a species- and stage-specific way. In the present paper we studied the egg and yolk-sac larval development of Pagellus erythrinus under different water temperature conditions, 15°C, 18°C and 21°C for the egg stage and 16°C, 18°C and 21°C for the yolk-sac larval stage. The temperature-independent thermal sum of development was estimated as 555.6 degree-hours above the threshold temperature (the temperature below which development is arrested), i.e. 7°C for the egg and 12.1°C for the yolk-sac larval stage. Higher hatching and survival rates occurred at 18–21°C. At the end of the yolk-sac larval stage, body morphometry differed significantly (p<0.05) between the temperatures tested. The growth rate of the total length increased as temperature rose from 16°C to 18°C, while in the range of 18–21°C it stabilized and was independent of water temperature. The estimated Gompertz growth curve for the yolk-sac larvae of P. erythrinus was (r²=0.992) for the 16°C, (r²=0.991) for the 18°C and (r²=0.981) for the 21°C treatment. The efficiency of vitelline utilization during the yolk-sac larval stage was higher at 18°C.Communicated by O. Kinne, Oldendorf/Luhe     

Effects of temperature and salinity on larval development ofNecora puber (Brachyura: Portunidae)

Temperature and salinity affected both length of larval development and mortality inNecora puber collected in the Ría de A Coruña during December 1984 and January 1985. Development time decreased considerably with increased temperature. This decrease was sharper when temperature increased from 15° to 20°C than when it increased from 20° to 25°C. At 35S, average development took 48, 32 and 28 d at 15°, 20° and 25°C, respectively. At the three salinities tested (25, 30 and 35), larval development was completed only at 15°C, at 20°C/30 and 35S, and at 25°C/35S. Development times at 15° and 20°C were highly significantly different at both 35 and 30S (P 0.01). However, there were no significant differences between development times at 20° and 25°C (P > 0.05). Within any one specific temperature series, no significant difference was observed between the salinity values tested (P > 0.05). The duration of each of the five zoeal stages was similar within each and the same temperature/salinity combination, whereas the duration of the megalop was twice as long as any of the zoeal stages. The combination of the lowest temperature (15°C) and the highest salinity (35) tested resulted in the greatest larval survival of 28%. Highest mortality occurred at 25°C, at which temperature development was completed only at 35S. A sharp drop in larval survival was observed in the transition period Zoea V — megalop in all combinations of temperature and salinity tested. Within the limits of tolerance to temperature and salinity, the former effected more pronounced differences in the duration of larval development, while salinity appeared to constitute a limiting factor for survival.     

Larval development of Pilumnoides perlatus (Brachyura: Xanthidae) under laboratory conditions

Larvae of the xanthid crab Pilumnoides perlatus (Poeppig, 1836) have been reared in the laboratory at 3 different temperatures (10.2°, 15° and 20°C) from hatching to megalopa stage. The 5 zoea stages and the megalopa, as well as the setation of the functional appendages are described and illustrated. The main characteristics useful to differentiate the larval stages of P. perlatus from those of Homalaspis plana, the other Chilean species of the same family so far reared, are discussed. Data on duration of zoea development, length of moulting intervals, and mortality at the 3 test temperatures are also given.This study was partially supported by the Chilean National Commission for Scientific and Technological Research (CONICYT).     

Feeding,growth, and survival of Engraulis mordax larvae reared in the laboratory

Methods are described for the successful rearing of northern anchovy larvae (Engraulis mordax Girard) on cultured foods. Larvae were fed successively on the unarmored dinoflagellate Gymnodinium splendens, the veliger of the gastropod Bulla gouldiana, and nauplii of the brine shrimp Artemia salina. Rearing containers ranging in capacity from 4.5 to 510 l were tested; the smaller ones were found to be most useful for laboratory experimentation. Irreversible starvation occurred when E. mordax were denied food for more than 1.5 days after yolk absorption. Growth rates of larval anchovies fed different diets were compared. Larvae fed G. splendens grew for 1 week at the same rate as animals fed wild plankton, but did not maintain this rate. Laboratory survival of E. mordax larvae on a diet of G. splendens alone, did not differ significantly when veligers supplemented the diet. However, when G. splendens and veligers were fed simultaneously to E. mordax larvae, growth rate was greatly improved, although still not matching the growth attained on a diet of wild plankton. Length (L) versus weight (W) analyses were made for all larvae at all diets. The results showed that weight could be calculated most accurately from length by the relationship log W=3.3237 log L-3.8205, regardless of diet.     

Unusual lecithotrophic development of the caribbean brittle star Ophiothrix oerstedi

The ophiuroid Ophiothrix oerstedi Lütken spawned in the laboratory at Barbados, West Indies, from August, 1975 until early December. The embryo passes through a wrinkled blastula stage, and the larva is a reduced lecithotrophic ophiopluteus with a shortened pelagic existence. A larva of this type is unusual for brittle stars in general and unique for ophiothricids for which development has been described. Metamorphosis is completed 4.3 days (24° to 27°C) after fertilization with a single pair of ciliated larval arms, the postero-lateral arms, being retained as a swimming device for the late larva. Settlement, with subsequent separation of the postero-lateral arms from the young brittle-star, begins as early as 4.5 days, but can be delayed for at least one week, at the end of which time midwater separation can occur resulting in the pelagic dispersal of post-larvae. A comparison of gametic and larval characteristics of O. oerstedi with the literature suggests that the larva of this species is most closely allied to the abbreviated developers. The adaptive significance of this larval form is discussed.     

Neue ergebnisse über die aufzucht von Carcinus maenas im laboratorium

The shore crab Carcinus maenas was reared in the laboratory from egg deposition to sexual maturity. Special enclosures were developed for cultivation of the larvae. Food and temperature proved to be the most important exogenous factors for rearing success. Fresh Artemia salina nauplii were the only food suitable for all larval stages. The following rearing temperatures proved most successful during larval development: (1) embryonic development, 10°C; (2) zoea stages, 15°C; (3) megalopa stage, 17.5°C. The larvae hatch preferably in darkness when reared under short-day conditions.     

Preliminary rearing experiments on the larvae of Sergestes lucens (Penaedia,Natantia, Decapoda)

Sergestes lucens Hansen, a mesopelagic shrimp fished commercially in Suruga Bay, Japan, was successfully reared from egg to post-larval stage V under laboratory conditions. Chaetoceros ceratosporum and Artemia nauplii were found to be satisfactory food in the laboratory during rearing. Growth, mortality, food preference, and feeding and swimming activities during the various developmental stages were investigated. Temperature changes greatly affected the speed of development and the mortality of the larvae. The optimum temperature range for larval development was 18° to 25°C. The growth rate (length) of larval stages was as rapid as 0.16mm/ day at 20 °C and 0.21 mm/day at 23 °C. The larvae first started feeding on phytoplankton at elaphocaris stage I, and then gradually became predators in the post-larval stages. It is suggested that the critical period for the species occurs in the elaphocaris stages. Environmental data, vertical distribution of the species, and data obtained from laboratory experiments suggest that the fluctuation in the abundance of S. lucens is greatly influenced by the water temperature at around 50 m from June to August. Feeding mechanisms observed in the post-larval stages are described.     

Food-particle size and selection by bivalve larvae in a temperate embayment

Epifluorescence microscopy was used to analyze the stomach contents of bivalve larvae collected in the Baie des Chaleurs (western Gulf of St. Lawrence, Canada) in order to document food-particle sizes, compare feeding among taxa, and compare the diet with the in situ phytoplankton community. Stomach contents were mainly composed of small autotrophic flagellates (<5 μm) and cyanobacteria (<2 μm), reflecting the microbial food web which characterizes these waters. More than half (55%) of all veligers examined contained algal cells of 5 to 15 μm, whereas only 3% had cells of 15 to 25 μm. Differences in the size ranges of ingested algal cells among similar-sized larvae of different species suggests that veligers actively selected food particles. Among the smallest veligers (185 to 260 μm), scallops (Placopecten magellicanus) and mussels (Mytilus edulis) ingested more <5 μm and 5 to 15 μm algae than clams (Mya arenaria). Among larger veligers (261 to 405 μm), clams contained significantly more <5 μm cells than mussels, whereas mussels contained significantly more 5 to 15 μm algae than clams. Algal cells of 15 to 25 μm were preferentially ingested by mussel veligers. Feeding also differed between different-sized veligers within taxa, i.e. the smallest clam veligers ingested fewer of 5 to 15 μm algae than the larger size classes. Mussel veligers ingested significantly more 15 to 25 μm and fewer <5 μm cells as their size increased. The dominance of ultraplankton in the nearshore waters of Baie des Chaleurs and in the stomach contents suggests that veliger larvae may be an important export path for carbon produced by small phytoplankton. Received: 17 July 1996 / Accepted: 20 September 1996     

A dispersal model for larvae of the deep sea red crab Geryon quinquedens based upon behavioral regulation of vertical migration in the hatching stage

Behavioral responses to gravity, hydrostatic pressure, and thermoclines are described for Stage I zoeae of the deep sea red crab Geryon quinquedens Smith. Survival and rate of development as a function of temperature is presented for all larval stages. Although temperatures between 10° and 25°C have no direct effect upon survival, development time is five times longer at 10°C than at 25°C. Stage I larvae show strong negative response to gravity. Swimming rate increases with an increase in pressure up to 20 atm above ambient at 11°C, but not at 15°C. Swimming rates at 15°C are higher than those measured at 11°C at each pressure tested. Stage I larvae readily penetrate sharp thermoclines. Potential dispersal ranges of G. quinquedens larvae in the Mid-Atlantic Bight are suggested based on larval behavior, development time, and coastal hydrography. A testable recruitment model is proposed for G. quinquedens.Contribution no. 1365 of the Center for Environmental and Estuarine Studies     

Larval development of the red crab Pleuroncodes monodon (Decapoda Anomura: Galatheidae) under laboratory conditions

Larvae of Pleuroncodes monodon (Milne-Edwards, 1837), a red crab of commercial importance in South America, were reared in the laboratory at 2 different temperatures (15° and 20°C), from hatching up to the last larval stage. The 5 typical stages, with their corresponding functional appendages, are described and figured. The main characteristics useful in differentiating larvae of P. monodon from those of the other Chilean species of Galatheidae and its northern congener P. planipes are discussed. Data on duration of each larval stage, length of moulting intervals and mortality at the 2 test temperatures are also given.This study was financially supported by the Chilean Ministry of Agriculture and by the National Commission for Scientific and Technological Research (CONICYT).