The effect of salinity and temperature on the larval development of Mithrax caribbaeus Rathbun, 1920 (Brachyura: Majidae) reared in the laboratory

Larvae of Mithrax caribbaeus were reared in the laboratoryin a factorial experiment employing three temperatures (22,25 and 28°C) and three salinities (32, 35 and 38). Survivaland duration of larval stages were recorded. Ovigerous femalesof M.caribbaeus were collected from the south-eastern coastof Margarita Island, Venezuela, and maintained in individualaquaria until hatching. Eggs from three of the females hatchedin the laboratory. Larvae from each hatching were subdividedinto groups of 10 and reared in plastic bowls containing 200ml filtered and UV-irradiated sea water at different temperature–salinitycombinations. Larvae were transferred daily to clean bowls withnewly hatched Artemia nauplii, and the number of molts and mortalitywithin each bowl was recorded. Complete larval development ofM.caribbaeus occurred under all experimental conditions. Salinityhad the greatest effect on percentage survival of each larvalstage and complete development up to the first crab stage. Thefirst zoeal stage exhibited the highest survival rate. Maximumsurvival for this stage occurred at 25°C, 32–35. Survivalin the second zoeal stage and the megalopa was affected onlyby salinity. Effects of temperature and salinity on survivaldecreased with advance in development. The duration of the twozoeal stages, the megalopa, and development to the first crabstage showed a gradual reduction with increasing temperature.Salinity showed an effect on the duration of zoeal stages butnot on the megalopal stage. Development from hatching to thefirst crab stage required 8–18 days, depending on thetemperature–salinity combination, and was inversely relatedto temperature, averaging 14.3 days at 22°C, 11.8 days at25°C and 9.2 days at 28°C.     

Early developmental stages of greasyback shrimp,Metapenaeus ensis (de Haan, 1844) (Crustacea, Decapoda, Penaeidae)

Metapenaeus ensis was spawned and laboratory cultured untilthe post-larval stage to illustrate and describe its embryonicand larval development. Fecundities ranged between 454 000 and689 000 eggs, and {small tilde}99.2% of spawned eggs hatchedafter 12 h and 40 min at 33.5 p.p.t. and 29.0-29.1°C. Sixnaupliar, three protozoeal, three mysis and one post-larvalstages were noted. A minimum of {small tilde}10 days (249 h20 min) from the time of hatching were required to completethe larval stages by subsisting only on Chaeioceros gracilisand Tetraselmis tetrathele at varying temperature and salinityof 28.1-29.8°C and 33.5—34.5 p.p.t., respectively.The embryonic and larval developmental stages of M.ensis aregenerally similar to those of other known penaeid species, exceptfor the size and structure of diagnostic characters, setationof appendages and duration of metamorphoses.     

Influence of temperature on larval survival, development, and respiration inChasmagnathus granulata (Crustacea, Decapoda)

Larvae of an estuarine grapsid crabChasmagnathus granulata Dana 1851, from temperate and subtropical regions of South America, were reared in seawater (32/%.) at five different constant temperatures (12, 15, 18, 21, 24 °C). Complete larval development from hatching (Zoea I) to metamorphosis (Crab I) occurred in a range from 15 to 24 °C. Highest survival (60% to the first juvenile stage) was observed at 18 °C, while all larvae reared at 12 °C died before metamorphosis. The duration of development (D) decreased with increasing temperature (T). This relationship is described for all larval stages as a power function (linear regressions after logarithmic transformation of bothD andT). The temperature-dependence of the instantaneous developmental rate (D ⁻¹) is compared among larval stages and temperatures using the Q₁₀ coefficient (van't Hoff's equation). Through all four zoeal stages, this index tends to increase during development and to decrease with increasingT (comparing ranges 12–18, 15–21, 18–24 °C). In the Megalopa, low Q₁₀ values were found in the range from 15 to 24 °C. In another series of experiments, larvae were reared at constant 18 °C, and their dry weight (W) and respiratory response to changes inT were measured in all successive stages during the intermoult period (stage C) of the moulting cycle. Both individual and weight-specific respiration (R, QO ₂) increased exponentially with increasingT. At each temperature,R increased significantly during growth and development through successive larval stages. No significantly differentQO ₂ values were found in the first three zoeal stages, while a significant decrease with increasingW occurred in the Zoea IV and Megalopa. As in the temperature-dependence ofD, the respiratory response to changes in temperature (Q₁₀) depends on both the temperature range and the developmental stage, however, with different patterns. In the zoeal stages, the respiratory Q₁₀ was minimum (1.7–2.2) at low temperatures (12–18 °C), but maximum (2.2–3.0) at 18–24 °C. The Megalopa, in contrast, showed a stronger metabolic response in the lower than in the upper temperature range (Q₁₀=2.8 and 1.7, respectively). We interpret this pattern as an adaptation to a sequence of temperature conditions that should typically be encountered byC. granulata larvae during their ontogenetic migrations: hatching in and subsequent export from shallow estuarine lagoons, zoeal development in coastal marine waters, which are on average cooler, return in the Megalopa stage to warm lagoons. We thus propose that high metabolic sensitivity to changes in temperature may serve as a signal stimulating larval migration, so that the zoeae should tend to leave warm estuaries and lagoons, whereas the Megalopa should avoid remaining in the cooler marine waters and initiate its migration to wards shallow coastal lagoons.     

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.     

Morphology of Coenophthalmus tridentatus first zoea (Crustacea: Portunidae: Polybiinae) hatched in the laboratory

The swimming crab Coenophthalmus tridentatus A. Milne Edwards,1879 (Decapoda, Portunidae) is an endemic species of the SouthwesternAtlantic, from southern Brazil to northern Patagonia (Argentina).Larvae of C. tridentatus from one female collected on beds ofoysters and mussels at 50 m depth in the Argentine continentalshelf (38°21'S, 57°38'W) were hatched in the laboratory.Zoea I morphology is described for the first time and comparedwith known zoeae of other portunid species.     

Growth, development and condition of Dendraster excentricus (Eschscholtz) larvae reared on natural and laboratory diets

Feeding invertebrate larvae may be food limited while developingin the ocean. If they are, then their time in the plankton isprolonged, which likely increases mortality. Food limitationcould be due to the quantity and/or quality of the food available.In an effort to answer how food type influences larval nutrition,we compared growth, development and lipid deposition for Dendrasterexcentricus larvae reared in natural seawater from two depths(1 and 20 m) and in filtered seawater on a monoculture laboratorydiet of 6 cells µL^–1 of the green alga Dunaliellatertiolecta (Butcher). Five days post-fertilization, larvaereared on the laboratory diet had developed to the latest stage,were the largest and had lipid deposits. Larvae reared on naturalsurface water were intermediate in size and developmental stage,and larvae reared in the water from 20 m depth were the smallestand developed the slowest. This trend continued at 8 days post-fertilizationwhen surface water diet larvae were similar in size to laboratorydiet larvae, but their juvenile rudiments were significantlysmaller. To assess food availability in each food treatment,we compared the concentration of chlorophyll (Chl) a, b andc in natural seawater from each depth and in D. tertiolectaculture in filtered seawater. Natural seawater collected fromthe surface had the highest concentration of Chl a and c, whereasChl b was not significantly different between treatments. IncreasedChl concentrations in the surface water are likely due to higherconcentrations of diatoms and dinoflagellates, which are typicallynot high-quality food items for echinoid larvae. Our resultssupport a hypothesis that echinoid larvae in the water columnmay be limited by food quality.     

Larval and early post-larval stages in the abbreviated development of Heterosquilla tricarinata (Claus, 1871) (Crustacea, Stomatopoda)

Heterosquilla tricarinata was laboratory-cultured through itscomplete larval development and found to have one propelagicand two pelagic larval stages prior to metamorphosis to thejuvenile. These larval stages, the first juvenile, and relevantportions of the second juvenile stage, are described and figured.Individual larvae do not change in size during intermoult periods.Larvae occurring in the plankton show a progressive decreasein mean size between early (September) and late (November) springtime.Reasons for this are suggested. The first pelagic stage of H.tricarinata is anatomically very advanced in development, andthe number of pelagic stages very few, in comparison with otherknown stomatopod life-histories. Ecological implications ofthis are discussed in relation to the high-latitude distributionof the species. Comparison is made between the final pelagicstage of H. tricarinata and that of its congenor H. brazieri. ^*Permanent address: Zoology Department, University of Queensland,Brisbane, Australia     

Complete larval and early juvenile development of the mangrove crab Perisesarma fasciatum (Crustacea: Brachyura: Sesarmidae) from Singapore, with a larval comparison of Parasesarma and Perisesarma

The complete larval development of the sesarmid crab Perisesarmafasciatum (Lanchester, 1900) from Singapore was obtained fromlaboratory culture. All four zoeal stages, the megalopa andthe first crab stage are described and illustrated. The morphologicalcharacteristics of the larvae of P. fasciatum are compared withthose of other known larvae of the genera Perisesarma and Parasesarma.The larval morphology of P. fasciatum clearly presents the typicalcombination of features that characterize sesarmid larvae. Overall,larval stages are very similar in Perisesarma and Parasesarmaand it is impossible to distinguish these two genera by larvalmorphology.     

Influence of temperature on growth, reproduction and longevity of Moina salina Daday, 1888 (Cladocera, Moinidae)

This paper presents the results of a study of the effects oftemperature on the growth, reproduction and longevity of thecladoceran Moina salina, a species of potential use as livefood in marine aquaculture. The growth rate of M.salina increasedwith increasing temperature. Some parameters of development,such as length at death and the number of adult instars, werealso positively related to temperature. Other parameters (durationof juvenile and adult instars) decreased with increasing temperature,while the number of juvenile instars was unaffected. An increasein temperature resulted in a reduction in age at maturity anda decrease in the number of days between broods. The numberof young per female, the number of broods per female, the numberof youngper day of reproductive life, and the number of youngper brood, increased up to a temperature of 25°C. At 15and 20°C. substantial degeneration of eggs and/or embryosoccurred. Likewise, temperature affected the type of reproductioncarried out by sexual females. Temperature and longevity wereinversely correlated. It was concluded that temperature actsas a very important factor regulating the life cycle of M.salina.Temperature >30°C may correspond to sublethal levels,while a temperature of 15°C is considered to impose stress.The range 20–25°C is optimal for the development andreproduction of this species.     

Complete larval development of the hermit crabs Clibanarius aequabilis and Clibanarius erythropus (Decapoda: Anomura: Diogenidae), under laboratory conditions, with a revision of the larval features of genus Clibanarius

The complete larval development (four zoeae and one megalopa) of Clibanarius aequabilis and C. erythropus, reared under laboratory conditions, is described and illustrated. The larval stages of the two northeastern Atlantic Clibanarius species cannot be easily differentiated. Their morphological characters are compared with those of other known Clibanarius larvae. The genus Clibanarius is very homogeneous with respect to larval characters. All Clibanarius zoeae display a broad and blunt rostrum, smooth abdominal segments and an antennal scale without a terminal spine. Beyond the second zoeal stage, the fourth telson process is present as a fused spine, and the uropods are biramous. In the fourth larval stage all species display a mandibular palp. The Clibanarius megalopa presents weakly developed or no ocular scales, symmetrical chelipeds, apically curved corneous dactylus in the second and third pereiopods, and 5–11 setae on the posterior margin of the telson. Apart from the number of zoeal stages, Clibanarius species may be separated, beyond the second zoeal stage, by the telson formula and the morphology of the fourth telson process.     

Larval salinity tolerance of the South American salt-marsh crab, Neohelice (Chasmagnathus) granulata: physiological constraints to estuarine retention, export and reimmigration

The semiterrestrial crab Neohelice (=Chasmagnathus) granulata (Dana 1851) is a predominant species in brackish salt marshes, mangroves and estuaries. Its larvae are exported towards coastal marine waters. In order to estimate the limits of salinity tolerance constraining larval retention in estuarine habitats, we exposed in laboratory experiments freshly hatched zoeae to six different salinities (5–32‰). At 5‰, the larvae survived for a maximum of 2 weeks, reaching only exceptionally the second zoeal stage, while 38% survived to the megalopa stage at 10‰. Shortest development and negligible mortality occurred at all higher salt concentrations. These observations show that the larvae of N. granulata can tolerate a retention in the mesohaline reaches of estuaries, with a lower limit of ca. 10–15‰. Maximum survival at 25‰ suggests that polyhaline conditions rather than an export to oceanic waters are optimal for successful larval development of this species. In another experiment, we tested the capability of the last zoeal stage (IV) for reimmigration from coastal marine into brackish waters. Stepwise reductions of salinity during this stage allowed for moulting to the megalopa at 4–10‰. Although survival was at these conditions reduced and development delayed, these results suggest that already the zoea-IV stage is able to initiate the reimmigration into estuaries. After further salinity reduction, megalopae survived in this experiment for up to >3 weeks in freshwater, without moulting to juvenile crabs. In a similar experiment starting from the megalopa stage, successful metamorphosis occurred at 4–10‰, and juvenile growth continued in freshwater. Although these juvenile crabs showed significantly enhanced mortality and smaller carapace width compared to a seawater control, our results show that the late larval and early juvenile stages of N. granulata are well adapted for successful recruitment in brackish and even limnetic habitats.     

Ingestion of Large Centric Diatoms, Mangrove Detritus, and Zooplankton by Zoeae of Aratus pisonii (Crustacea: Brachyura: Grapsidae)

Ingestion rates of zoeae of Aratus pisonii Milne Edwards (Brachyura: Grapsidae) were determined offering natural plankton-detritus mixtures in laboratory food selection experiments. The food mixtures were sampled in the Itamaracá estuary, north-eastern Brazil, and standardised to a size range of 50–200 μm. Zoeae ingested significant amounts of large centric diatoms (Coscinodiscus spp.), mangrove detritus, tintinnids (Favella ehrenbergi) and adult copepods during feeding experiments. Diatoms were positively selected by A. pisonii zoeae in all three experiments, with ingestion rates of 3.3–21.3 cells zoea⁻¹ day⁻¹. Detritus particles were always more abundant than phytoplankton and zooplankton in the particle size spectrum offered. Detritus was ingested in two of three experiments, with ingestion rates of up to 34.1 particles zoea⁻¹ day⁻¹, being the most important food item during one experiment. Adult copepods (up to 1.8 ind. zoea⁻¹ day⁻¹) and tintinnids (up to 0.4 ind. zoea⁻¹ day⁻¹) were ingested by A. pisonii zoeae during one experiment each. In spite of a wide range of zoeal density, food particle composition, and density, zoeae of A. pisonii displayed a consistent pattern of food selectivity. This hints at a consistent sensory and behavioural mechanism related to capture and handling of food particles, that most likely also affects larval feeding under natural conditions. Although detritus showed to be quantitatively ingested under estuarine conditions, zoeae of A. pisonii preferred large diatoms and ingested zooplankton only occasionally.     

Larval development of Brachynotus gemmellari (Rizza, 1839) (Brachyura, Grapsidae) reared under laboratory conditions

The complete larval development of the grapsid crab Brachynorusgemmellari (Rizza, 1839) was obtained by culture in the Iabomtoiy.Five zoeal stages, the megalopa and the first crab stage aredescribed and illustrated. Larval development from hatchingto first crab took 26 days at 20C. The morphological charaeiarsof the larvae of B.gemmellari are compared with those of otherknown larvae of the genus Brachynosus.     

Seasonal species composition of barnacle larvae (Cirripedia: Thoracica) in Rhode Island waters, 1977-1978

Cirripede larvae can occur year-round in temperate and tropicalwaters, often in significant numbers, yet the species compositionof the ‘Balanus sp.’ component is rardy studied.Weekly plankton samples were analyzed qualitatively for larvalcirripede species and stage over a year (1977–1978) attwo Rhode Island stations. Six species of larvae were foundin Lower Narragansett Bay (30° salinity). Semibalanus balanoidesand Balanus balanus have a single winter brood. S. balanoidesis the predominant winter breeder with a minor release of naupliiin early December and major release in March followed by cypridsin mid-April.B. balanus populations release all larvae in Marchwith cyprids in mid-April. Balanus crenatus is mainly a winterbreeder, but has multiple broods; it does not breed in July-Septemberwhen the water temperature is above 18°C. Balanus venustusis the predominant summer breeder, and larvae were observedfrom May through December (water >8°C). Larvae of Chthamalusfragilis and Balanus eburneus occur in low numbers from May-October.At the Pettaquamscutt River site (12 salinity), Balanus improvisuslarvae predominate and early stage nauplii (I-II) occur in samplesyear round (0–27°C). Two peaks of later stage naupliiand cyprids occur in late spring (May) and early winter (Nov.-Jan.).Continued temperatures bdow 5°C or above 20°C appearto inhibit larval development. Comparison of results with existing literature reveals severalsignificant findings. The bimodal rdease of S. balanoides larvaeis unusual and may be in response to the phytoplankton dynamicsof the year; however, the existence of distinct races of S.balanoides may also be a factor. Larvae of B. venustus predominatein the lower bay during the summer, yet this species is unreportedin past studies. B. improvisus nauplii are more cold tolerantthan previously reported. Comparison of findings with reportedbreeding patterns in Florida indicate significant differencesin temperature responses between northern and southern populations. ¹Contribution No. 188 from EPA Environmental Research Laboratory,South Ferry Rd., Narragansett, RI 02882     

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.     

Seasonal and tidal abundance patterns of decapod crustacean larvae in a shallow inlet (SW Spain)

Planktonic larvae of decapod crustaceans were collected monthlyfrom July 1991 to June 1992 by pumping during nocturnal floodand ebb tides to establish seasonal larval abundance patternsin an inlet of the Bay of Cdiz. Additional 24 h series of sampleswere collected seasonally (July 1991, October 1991, January1992 and May/June 1992) during spring and neap tides to analyselarval abundance in relation to the main environmental cycles(diel, tidal and lunar phases) and vertical position in thewater column. First zoeae were the most abundant stage for mostspecies, representing 97.6% of all individuals collected. ZoeaI abundance was higher in spring and swmner and, on most samplingoccasions, there was a net output from the inlet to the bay.Five species (Liocarcinus arcuatus and Liocarcinus vernalis,Uca tangeri, Diogenes pugilator and Panopeus africanus) represented60% of total individuals caught. The seasonal occurrence offirst zoeae of the most abundant species indicated two differentreproductive patterns: species with a short reproductive periodand species spawning year round. Zoea I of several species (Panopeusafricanus, Uca tangeri, Pachygrap sus marmoratus, Processa spp.)were significantly more abundant during ebb tides and theirlater larval stages were scarcely collected, suggesting thatthese larvae are released in the inlet and exported to the bay.Conversely, a net input of first zoeae was observed for otherspecies (D.pugilator and Pinnotheres pinnotheres), but theirlater larval stages were also scarcely collected. Such importationcould be a larval rhythm artifact due to release of larvae inthe bay that drifted into the inlet by tidal currents. The crabIlia nucleus, whose later larval stages were collected frequently,was the only species that seemed to complete its life cyclewithin the bay. These results suggest that the studied inletwas primarily used by decapods as an adult habitat and spawningground, while larval development occurred in open sea. Sincevertical migration was not observed for exported larvae, thetidal synchronization of female release seemed to be the mostprobable mechanism of larval exportation. There were no significantdifferences between larval release during spring and neap tides.     

Larval and early juvenile development of Lithodes santolla (Molina, 1782) (Decapoda: Anomura: Lithodidae) reared at different temperatures in the laboratory

The southern king crab, Lithodes santolla Molina, is distributed in cold-temperate and subantarctic waters ranging from the southeastern Pacific island of Chiloé (Chile) and the deep Atlantic waters off Uruguay, south to the Beagle Channel (Tierra del Fuego, Argentina/Chile). Recent investigations have shown that its complete larval development from hatching to metamorphosis, comprising three zoeal stages and a megalopa, is fully lecithotrophic, i.e. independent of food. In the present study, larvae were individually reared in the laboratory at seven constant temperatures ranging from 1 to 18 °C, and rates of survival and development through successive larval and early juvenile stages were monitored throughout a period of 1 year. The highest temperature (18 °C) caused complete mortality within 1 week; only a single individual moulted under this condition, 2 days after hatching, to the second zoeal stage, while all other larvae died later in the zoea I stage. At the coldest condition (1 °C), 71% of the larvae reached the zoea III stage, but none of these moulted successfully to a megalopa. A temperature of 3 °C allowed for some survival to the megalopa stage (17-33% in larvae obtained from two different females), but only a single individual passed successfully, 129 days after hatching, through metamorphosis to the first juvenile crab instar. At all other experimental conditions (6, 9, 12 and 15 °C), survival through metamorphosis varied among temperatures and two hatches from 29% to 90% without showing a consistent trend. The time of nonfeeding development from hatching to metamorphosis lasted, on average, from 19 days at 15 °C to 65 days at 6 °C. The relationship between the time of development through individual larval or juvenile stages (D) and temperature (T) was described as a power function (D=aT^b, or log[D]=log[a]blog[T]). The same model was also used to describe the temperature dependence of cumulative periods of development from hatching to later larval or juvenile stages. One year after hatching, the 7th (6 °C) to 9th (15 °C) crab instar was reached. Under natural temperature conditions in the region of origin of our material (Beagle Channel, Argentina), L. santolla should reach metamorphosis in October-December, i.e. ca. 2 months after hatching (taking place in winter and early spring). Within 1 year from hatching, the crabs should grow approximately to juvenile instars VII-VIII. Our results indicate that the early life-history stages of L. santolla tolerate moderate cold stress as well as planktonic food-limitation in winter, implying that this species is well adapted to subantarctic environments with low temperatures and a short seasonal plankton production.