Larval development of Ocypode quadrata (Brachyura: Crustacea) under laboratory conditions

The larvae of Ocypode quadrata (Fabricius) have been reared in the laboratory, from hatching to megalopa stage, at 35 S, 25°C. The five zoeal stages and the megalopa are described, including functional appendages of each stage. On the basis of morphological characteristics, the first zoeal and megalopa stages of O. quadrata can be distinguished from similar stages of closely related Ocypodinae. At 25°C, the megalopa appeared in a minimum of 34 days following hatching.     

Larval development of the spider crab Pisoides edwardsi (Decapoda,Brachyura) under laboratory conditions

Larvae of Pisoides edwardsi (Bell, 1835) have been reared in the laboratory at 2 different temperatures (13.8° and 18.5°C), from hatching to megalops stage. The two zoeal stages and the megalops, as well as the setation of the functional appendages are described and illustrated. The main characteristics useful to differentiate the larvae of P. edwardsi from those of Libidoclaea granaria, the other Chilean species belonging to the same sub-family, are discussed. Data on duration of zoeal development, length of moulting intervals, and mortality at the 2 test temperatures, are also given.This study was financially supported, in part, by the Chilean Ministry of Agriculture.     

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).     

Larval development of the hermit crab Clibanarius albidigitus (Crustacea: Anomura: Diogenidae) reared under laboratory conditions

The larval development of Clibanarius albidigitus Nobili is described and illustrated from laboratory-reared specimens. At 30°C, this species passes through four zoeal stages before molting to the megalopa. Of the 120 individual larvae reared, survival was high, with 88% reaching the megalopal stage. Zoeal stage durations varied from 3 to 18 d. Rearing was terminated after 45 d, and at that time no megalopae had molted to the firstcrab stage. Among known larvae of Clibanarius species, C. albidigitus is immediately distinguished by the presence of dorsomedial and dorsolateral carapace keels.     

The effect of salinity and cyclic temperature on larval development of the mud-crab Rhithropanopeus harrisii (Brachyura: Xanthidae) reared in the laboratory

Larvae of Rhithropanopeus harrisii (Gould) were reared from hatching to the first or second crab stages in 11 combinations of salinities and cyclic temperatures (5, 20, and 35 S at 20° to 25°C, 25° to 30°C, and 30° to 35°C; 25 S at 20° to 25°C and 30° to 35°C). The larvae survived to the megalops and first crab stages in all salinities and cycles of temperature other than 5 S at 30° to 35°C. The best survival to the megalops (94%) and first crab (90%) stages occurred in 20 S, 20° to 25°C. In all other combinations of salinities and temperatures there was a reduction in survival to the first crab stage. The duration of the larval stages was affected significantly by temperature, whereas the effect of salinity on the mean days from hatching to the first crab stage was not consistent at the different temperature cycles. Development to the first crab stage required the shortest time in 20 S, 30° to 35°C (mean 12.3 days), and the longest time in 5 and 35 S, 20° to 25°C (mean 22.6 days and 21.6 days, respectively). Megalops larvae reared in 35 S at all cycles of temperature, as well as larvae in 20 and 25 S, 30° to 35°C, showed a high percentage of abnormality, with the highest percentage occurring in 35 S, 30° to 35°C. It appears that larval development of R. harrisii is strongly influenced by environmental factors and not solely related to genetic differences.This research was supported by grants from the Nordic Council for Marine Biology and the U.S. Atomic Energy Commission [Grant No. At-(40-1)-4377].Contribution No. 116, Zoological Museum, University of Oslo, Norway.     

Behavioral responses of a larval crustacean to hydrostatic pressure: Rhithropanopeus harrisii (Brachyura: Xanthidae)

Responses of the four zoeal stages of the crab Rhithropanopeus harrisii (Gould) to step and continuous changes in hydrostatic pressure were analyzed with a video system. Crabs were collected from the Neuse River estuary (North Carolina, USA) from June to August, 1987. The lower thresholds for step increases and decreases in pressure were 3 and 8 to 10 mbar, respectively. There was little change in sensitivity with zoeal development. Tests of larval responses in a light field that simulated the underwater angular light distribution indicated positive phototaxis does not occur upon pressure changes. In darkness, rates of pressure increase at and above 0.175 mbar s^-1 induced high barokinesis and negative geotaxis in all but Stage IV zoeae, which had a threshold of 1.19 mbar s^-1. Since larval sinking and descent swimming speeds exceed these threshold rates, larvae can move rapidly enough to produce suprathreshold changes in pressure which evoke behavioral responses. Slow rates of pressure decrease induced passive sinking while rapid rates caused an active ascent. This ascent response upon a pressure decrease is unreported among crustaceans, and is hypothesized to function for avoidance of feeding and respiratory currents of benthic invertebrates. The descent response occurs in all zoeal stages, except IV, at rates of pressure decrease (0.4 to 0.71 mbar s^-1) that are within the range of ascent swimming speeds. These results support Sulkin's negative feedback depth regulation model. The absolute distances moved before corrective vertical responses to threshold rates of pressure change are initated delimit the depth regulatory window. In darkness, the asymmetry of the window would lead to an ascent. It is hypothesized that light is an additional component in depth regulation, and that the limits and symmetry of the depth regulatory window may be controlled by the level of light adaptation.     

Behavioral responses of larvae of the crab Rhithropanopeus harrisii (Brachyura: Xanthidae) during diel vertical migration

Larval Rhithropanopeus harrisii (Gould) show nocturnal vertical migration. Larval behavioral responses to different rates of increase and decrease in light intensity were measured in an apparatus with a natural angular light distribution. A central objective was to establish whether phototaxis actually participates in vertical migration. At sunset the level of light adaptation controlled the readiness of the larvae to migrate, while an ascent was initiated by a preductable relative decrease in intensity (e.g. 4.0x10^-3s^-1). Rates of relative decrease around sunset would evoke continuous upward swimming. Gravity was the orienting cue and there was no change in swimming speed during the ascent. At sunrise, the larval descent was initiated by exposure to an absolute light intensity of about 0.23 log unit above the lower visual threshold. Light served as an orienting cue, as larvae descended by a negative phototaxis. Thus, phototaxis is not a laboratory artifact and does participate in vertical migration. A consideration of behavioral responses of other crustacean zooplankton indicates there is considerable variation in the initiating and directing cues for vertical movements. The variety of behavioral responses of R. harrisii suggests that a synthesis of hypotheses about migration may provide the proper basis for explaining the mechanisms underlying diel vertical migration.     

Population genetics of eight species of Trapezia (Brachyura: Xanthidae), symbionts of corals

Starch-gel electrophoresis was used to study gene-enzyme variation in thirteen populations of eight species of the genus Trapezia from Hawaii, Panamá, and Enewetak Atoll (Marshall Islands). Between 20 and 30 (mean = 27.8) gene-enzyme systems were resolved in each population, with 20 systems in common among all populations. The distribution of electrophenotypes was in agreement with Hardy-Weinberg-Castle expectations, except for T. digitalis, which consistently showed heterozygote deficiencies. Diagnostic loci among color forms support the hypothesis that color forms are distinct species. Low values of genetic distance among species suggest a recent radiation, perhaps during the Pleistocene. Genetic distance between the Hawaiian and Panamanian populations of T. ferruginea did not significantly differ from zero, indicating that the Eastern Pacific population of T. ferruginea has recently immigrated from the central Pacific, and/or that there is gene flow between the two areas. There were diagnostic loci between T. ferruginea and T. formosa from Enewetak and the populations of these species from Hawaii (T. ferruginea only) and Panamá (both species). Therefore, these geographic populations may represent separate species. The level and pattern of genetic variability in Trapezia spp. are in agreement with those observed in most other organisms.     

Entrainment of the larval release rhythm of the crab Rhithropanopeus harrisii (Brachyura: Xanthidae) by cycles in salinity change

Influences of salinity, Na, K, Ca and Mg on Na–K-ATPase activity in the posterior gills of Carcinus maenas (L.) have been investigated with respect to the role of the enzyme in hyperosmotic regulation. K and Mg ions were obligatory for enzyme activity. The dependence on the K concentration can be seen in a saturation curve of the Michaelis-Menten type. Low concentrations of Ca (0.2–3 mM) in the incubation medium strongly inhibited Na–K-ATPase activity. Activities inhibited by Ca could be reactivated to non-inhibited values by the addition of higher amounts of Mg (25 mM). Activity increased along with the salinity of the sea water used as incubation medium up to about 10 S. Here, maximum activity was observed. Further salinity increases of the incubating sea water were inhibitory. Salinity dependence is assumed to be based on Na dependence of the Na-pump. Comparative investigations of the Na–K-ATPase activity and its affinity to sodium in five species of decapod crustaceans indicated that levels of Na–K-ATPase differed in the posterior gills of stenohaline and euryhaline species. The results obtained confirm previous assumptions of a central role of the branchial Na–K-ATPase in hyperosmotic regulation. Properties of the Na–K-ATPase, such as affinity for substrates or dependence on ionic sea water constituents, are kept constant with respect to salinity changes. Modifications due to salinity only concern enzyme amounts especially in the posterior gills. The finding that the Na-pump is localized in basolateral parts of ion-transporting epithelial cells confirms the aforementioned results.     

Larval development of Euphausia nana (Crustacea: Euphausiacea)

The larvae of Euphausia nana Brinton in Sagami Bay and Suruga Bay, Central Japan, are described and illustrated. The furcilia stage is separated into six stages on the basis of the form of the pleopods and the number of terminal telson spines. Furcilia I, no pleopod or non-setose pleopods and seven terminal telson spines. Furcilia II, nonsetose and setose pleopods and seven terminal telson spines. Furcilia III, five pairs of setose pleopods and seven terminal telson spines. Furcilia IV, five pairs of setose pleopods and five terminal telson spines. Furcilia V, five pairs of setose pleopods and three terminal telson spines. Furcilia VI, five pairs of setose pleopods and one terminal telson spine. Segmentation of the antennal endopod and mandible palp occurred at the furcilia V stage. The dominant forms of early furcilia larvae of E. nana differed during different seasons of the year. The total lengths of calyptopis III and furcilia I to VI larvae also showed seasonal changes; they were largest in May and smallest from September to December.     

Phylogeny and geographic differentiation of Atlanto–Mediterranean species of the genus Xantho (Crustacea: Brachyura: Xanthidae) based on genetic and morphometric analyses

The crab genus Xantho Leach, 1814 is restricted to the northeastern Atlantic Ocean and the Mediterranean Sea. It consists of four species, Xantho hydrophilus (Herbst, 1790), X. poressa (Olivi, 1792), X. pilipes A. Milne-Edwards, 1867, and X. sexdentatus (Miers, 1881). X. hydrophilus has been divided into two geographic forms, of which one, X. h. granulicarpus (Forest, 1953), is postulated to be endemic to the Mediterranean Sea. In this study, we reconstruct phylogenetic relationships of the genus Xantho and related genera from the Atlantic Ocean or Mediterranean Sea and compare different geographic populations of Xantho hydrophilus and, to a lesser extent, of X. poressa by means of population genetic and morphometric analyses. The molecular phylogeny is based on two mitochondrial genes (large subunit rRNA and cytochrome oxidase I) and indicates that X. poressa, X. hydrophilus and X. sexdentatus form a monophyletic group, the latter two species sharing identical haplotypes. On the other hand, X. pilipes shows affinities to Xanthodius denticulatus. Population genetics based on the COI gene reveal genetic differentiation within X. hydrophilus. Morphometric results also give evidence for distinct geographic forms in X. hydrophilus with a clear discrimination. In comparison, morphometric discrimination between different geographic populations of X. poressa is less clear, but still significant. We therefore suggest a recent/ongoing morphological and genetic differentiation within Xantho hydrophilus, restricted gene flow between its Atlantic and Mediterranean populations (not allowing subspecific differentiation) and possible mtDNA introgression between the species X. hydrophilus and X. sexdentatus.     

Growth and reproduction of Pycnogonum litorale (Pycnogonida) under laboratory conditions

The complete life cycle of Pycnogonum litorale Ström was observed under laboratory conditions. At 15?°C and a 16?h light:8?h dark photocycle, the duration of embryonic development from oviposition to egg-hatching varied from 32 to 111?d. The onset of egg hatching ranged from 32 to 81?d after oviposition in different egg batches, and the period between the first and the last hatch within a single egg batch varied between 16 and 57?d. The larval period, consisting of five larval instars, lasted between 66 and 113?d. Juvenile development required seven (exceptionally 8 or 9) moults and lasted between 263 and 400?d. The average interval between successive moults in juveniles increased with increasing size from 24 to 82?d. Though females did not moult more often than their male conspecifics, they reached a size from 8.5 to 11.0?mm (average 10.1?mm) while adult males measured only 7.0 to 8.5?mm (average 7.7?mm). At low temperatures (2?°C) moulting was almost completely inhibited. After raising the temperature to 6?°C, the moulting frequency increased to a rate almost as high as at a constant temperature of 15?°C. Moulting was also retarded by starvation and accelerated by subsequent feeding. Adults lived for up to 9?years without further moults, with several periods of mating and oviposition at irregular intervals. In combination with previous long-term field observations, the present results provide a more complete picture of the life cycle of P. litorale in a natural habitat. The great variation in the duration of the different developmental stages, the ability to survive periods of cold and starvation, and the longevity of the adults are important for the survival of pycnogonid populations under changing environmental conditions.     

Acute toxicity of pentachlorophenol (PCP) on goldfish (Carassius auratus) under laboratory conditions

The U.S. Environmental Protection Agency (E.P.A.) recognized PCP as an environmental pollutant in need of control. Temperature and hardness were two controlling factors in PCP toxicity to fish.

Information on acute toxicity may provide the upper bounderies of dose‐response relationships.

Adult goldfish (Carassius auratus) were used to determine acute toxicity to 24, 48, 72 and 96 h LC50 for PCP.

Natural degradation and persistence of PCP in experimental water was also determined at pH 8.4 and two temperatures (22 and 29 °C).     

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 in the Antarctic nemertean Parborlasia corrugatus (Heteronemertea: Lineidae)

Embryonic and larval development were followed from fertilisation to settlement in the Antarctic heteronemertean Parborlasia corrugatus (McIntosh, 1876). The first cleavage occurred 10 to 15 h after fertilisation, and the second at 17 h. Larvae hatched at the gastrula stage, between 170 and 200 h post-fertilisation, and were 150 m in diameter. Early larval stages aggregated in dense groups near the surface of incubation vessels and were positively phototactic. Early pilidium larvae were recognisable 435 h post-fertilisation. They were 155×152 m in size, and possessed a complete apical tuft of cilia and a full marginal band of locomotory cilia. At this stage, the gust was visible through the body wall, and the mouth was open and was 40 m in diameter. Late pilidia, 222×193 m in size, were helmet-shaped. They had an apical tuft over 100 m long, and possessed a lobed marginal band of locomotory cilia. Pilidia were observed aggregating close to the bottom of incubation vessels 1200 to 1350 h (50 to 56 d) after fertilisation, and this was interpreted as settlement behaviour. At this stage, the apical tuft had been lost and they were highly contractile, being capable of compressing their bodies. However, neither developing juveniles within the larval envelope nor hatched juveniles were observed. Pilidia consumed the microalgae Tetraselmis suecica, Thalassiosira pseudonana and Isochrysis galbana. They also fed on particulate organic material < 1 m in size, as shown by the presence of material in the guts of larvae offered filtered extracts of algal cultures. There was some indication that larvae could use dissolved organic material, since pilidia held in seawater with organic material removed did not survive as long as those in filtered seawater or in filtered water with added amino acids. However, the only larvae to exhibit settlement behaviour in the feeding experiments were those offered Tetraselmis succica and Thalassiosira pseudonana, and these required a longer development time to reach this stage than pilidia in the standard cultures, where a mixed algal diet was offered.     

Entomotoxic effect of silicon dioxide nanoparticles on Plutella xylostella (L.) (Lepidoptera: Plutellidae) under laboratory conditions

The use of higher dosage and repeated applications of conventional pesticides have led to the rapid development of insect resistance to pesticide and adverse effects on human health and environment. Accordingly, researchers are prompted to identify an alternative entomotoxic agent for crop protection. Nanocides are being considered as alternatives to conventional insecticides because they are expected to lessen the application rate and reduce the chances of resistance development in pests. In this study, we evaluated the entomotoxic effects of nanosilica on larvae of Plutella xylostella, in a laboratory by using dust spray, larva dipping, leaf dipping, and solution spray methods. Dust treatment showed a more highly significant effect than the other three treatments. The mortality percentage increased up to 58% and 85% at 24 and 72 h after treatment, respectively, when nanosilica was applied at a rate of 1 mg cm^?2. In all four bioassays, mortality rate increased with both increased time after nanosilica exposure and increased concentration. Light microscopy and scanning electron microscopy images showed that larval death was due to desiccation, body wall abrasion, and spiracle blockage. These results suggested that nanosilica can be an alternative to conventional pesticides if dust formulation would be properly used.     

Mating behaviour of Macrophthalmus hirtipes (Brachyura: Ocypodidae)

 We examined the mating behaviour of the New Zealand ocypodid crab Macrophthalmus hirtipes in the laboratory between February and June 1998. This species has a discrete breeding season. Mating and moulting were not linked and only intermoult females with mobile gonopore opercula were attractive to males. Allometry and compatibility of gonopods and gonopores of different-sized crabs was investigated. Under laboratory conditions, the opercula of intermoult females remained mobile on average for 11.4 d, but the duration of receptivity did not appear to be under female control. The operational sex ratio in the laboratory fluctuated greatly, but was always male-dominated. During the period of opercular mobility, females mated many times with several different males. Matings in the absence of burrows were relatively short (mean duration = 23 min, max. = 122 min) and the mating behaviour of M. hirtipes lacked courtship and mate-guarding. Males used a search-intercept method to acquire mates, with very low levels of intrasexual competition. There was no evidence of mate preference in M. hirtipes, and males spent just as long mating with ovigerous females as with non-ovigerous ones. Although M. hirtipes has ventral-type spermathecae, as do several other ocypodid crabs, it is unclear whether this promotes last-male sperm precedence. The role of burrows in modifying the mating behaviour of M. hirtipes in the field remains to be established. Received: 7 January 2000 / Accepted: 5 June 2000     

Acquisition and loss of cold-tolerance in adult barnacles (Balanus balanoides) kept under laboratory conditions

In the laboratory, Balanus balanoides (L.) barnacles maintained without food at 5°C over the winter to summer period remained cold-tolerant. Winter animals maintained at 5°C and fed Artemia nauplii under a controlled light-dark regime until mid-summer lost this cold-tolerance. Summer animals, maintained without food at 5° or 15°C until midwinter, became cold-tolerant. Summer and winter animals subjected to increased (or decreased) ambient salinity for 48 h showed a small decrease (or increase) in their lower median lethal temperature (MLT—defined as the temperature at which 50% of the animals die after 18 h exposure to air). Summer animals subjected to desiccation for 48 h also showed a small decrease in their lower MLT. It is concluded that the seasonal changes in cold-tolerance of adult barnacles are probably induced by a combination of environmental factors including food availability, light intensity, day-length and changes in ambient sea-water temperatures. Development of cold-tolerance in the winter did not depend upon fertilisation. Changes in intra-cellular solute concentration which accompany adaptation to changes in ambient salinity or desiccation do not appear to be related to the seasonal changes in cold-tolerance.