Effect of hatching time on larval mortality and survival of the prawn Macrobrachium idae

The prawn Macrobrachium idae Heller carries 40 to 160 eggs depending upon the body size of the mother animal. After incubation, 63, 35 and 2% eggs are hatched on the first, second and third hatching nights, respectively. Mean dry weight of a single larva relased on the first night is 420 g (equivalent to 2.86 cal). Larvae released on the second or third hatching nights weighed 380 g (=2.56 cal) or 308 g (=2.02 cal). The total reserve yolk-energy available in a larva hatched on the first night is 1 cal. There is a definite shift from protein to fat metabolism as hatching is delayed. Oxygen consumption of developing eggs awaiting release on the first or second hatching night is 1.9 l/mg dry weight/h. In comparison to larvae released on the first night, those released on the second night exhibit 2% increase in total body-length and 2.4 or 14.3% decrease in the lengths of the 6th abdominal segment or the orbit. Larvae released on the first, second or third hatching nights, on exposure to starvation stress, survive for 3.8, 2.3 or 1.5 days. The swimming speed of larvae released on the first or second night is 1.0 or 0.6 cm/sec. Larvae released on the subsequent hatching nights committed nearly 2 times greater number of mistakes per cm distance in the horizontal plane. Since hatching of all developing eggs simultaneously on the first hatching night is possible by means of artificial technique(s), it is possible to improve survival rate of decapod larvae.     

Yolk utilization and hatching time in the Canadian lobster Homarus americanus

During the course of its embryonic development, the Canadian lobster Homarus americanus Milne-Edwards exhibits steady increases in water content (56.2 to 86.8%) and ash (5.8 to 21.2%), and a progressive decrease in energy content from 6636 to 4292 cal/g dry weight. Mean dry weight of a single egg is 965 g, equivalent to 6.4 cal; a freshly hatched egg. The lobster hatches about 1,500 larvae per night over a period of 4 to 5 days. Dry weight, ash and calorific contents of larvae hatched on different days show considerable variations. After larvae hatch on the first day, continuous salt absorption by eggs to hatch on subsequent days leads to a steady increase in ash content from 143 g/larva hatched on the first day to 255 g/larva hatched on the fourth day, and consequently, to an increase in dry weight from 854 to 956 g/larva. Metabolism of embryos (0.1 cal/day), which are yet to be hatched on subsequent days, depletes the calorific content per unit weight (from 4637 to 3837 cal/g dry weight) as well as per larva (from 3.98 to 3.67 cal).Dedicated to my colleague K.-H. Schumann (Biologische Anstalt Helgoland) who died on December 12, 1969 due to a diving accident.     

Food selection by laboratory-reared larvae of the scaled sardine Harengula pensacolae (Pisces,Clupeidae) and the bay anchovy Anchoa mitchilli (Pisces,Engraulidae)

Food selection by laboratory-reared larvae of scaled sardines Harengula pensacolae, and bay anchovies Anchoa mitchilli, was compared. Natural plankton was fed to the larvae during the 22 days following hatching. Food levels in the rearing tanks were maintained at an average of 1,600 to 1,800 potential food organisms per liter. Larvae of both species selected as food copepod nauplii, copepodites, and copepods; initial feeding was on organisms of 50 to 75 body width. Larvae of H. pensacolae averaged 4.2 mm in total length at hatching and those of A. mitchilli about 2.0 mm. H. pensacolae larvae grew about 1.0 mm per day and A. mitchilli 0.70 mm per day. The mean number of food organisms in each digestive tract was greater in H. pensacolae than in A. mitchilli, and the difference in number increased as the larvae grew. Average size of food organisms eaten increased for both species with growth, because of selection by the larvae; the average size of copepodites and copepods in digestive tracts increased at a faste rate in H. pensacolae than A. mitchilli. A. mitchilli longer than 8 mm did not eat copepod nauplii.Contribution No. 170, Bureau of Commercial Fisheries Tropical Atlantic Biological laboratory, Miami, Florida 33149, USA.     

Feeding behaviour and prey size selection of gilthead seabream,Sparus aurata,larvae fed on inert and live food

Prey selection shortly after the onset of feeding by laboratory-reared gilthead seabream, Sparus aurata L., larvae was studied using larvae fed on two types of microcapsule (hard- and soft-walled) having diameters ranging from 25 to 300 m. Preferences between inert food and live prey (rotifers and Artemia sp. nauplii) were also studied. Seabream larvae were able to ingest inert food from first feeding. Larvae of all size classes ingested hard microcapsules with diameters in the range 25 to 250 m. However, larvae with a total length (TL) below 4 mm preferentially selected particles 25 to 50 m in diameter, larvae of TL 4 and 5 mm preferred particles 51 to 100 m in diameter, while larvae above 5 mm TL preferred particles 101 to 150 m in diameter. With soft microcapsules, larvae always preferred particles larger than in the previous case, and above 4.5 mm TL they preferentially selected particles 201 to 250 m in diameter. In addition, the gradual increase of preferred diameters with increasing TL was more pronounced when larvae were increasing TL was more pronounced when larvae were fed on soft particles. Mean values for prey width/mouth width ratios were approximately 0.24 and 0.30 when larvae were fed on hard-walled and soft-walled microcapsules, respectively, irrespective of the absolute value of larval length. When a mixed diet of live and inert food items was offered, live prey were always preferentially selected, even if the prey width/mouth width ratio was apparently not favourable. Only a physical constraint such as excessive prey width could counter this preference for living prey vs inert microcapsules. These results contribute to our knowledge in larval feeding behaviour, especially in the presence of inert food, and represent a fundamental step in developing prepared food for marine fish larvae.     

Grazing and ingestion rates of nauplii,copepodids and adults of the marine planktonic copepod Calanus helgolandicus

The average grazing and ingestion rates of all stages of the marine planktonic copepod Calanus helgolandicus (Calanoida) from nauplius stage IV to adults were measured experimentally at 15°C in agitated cultures. The chain-forming diatom Lauderia borealis and the unarmoured dinoflagellate Gymnodinium splendens were offered as food. The food concentrations were close to natural conditions and ranged from 36 to 101 g of organic carbon per liter. The medium body weights expressed in g of organic carbon of almost all larval stages raised at 49 g C/1 were identical with the weight of the same stages caught in the Pacific Ocean off La Jolla, California, USA. In a log-log system, grazing and ingestion rates increased almost linearly with increasing body weight. Grazing rates ranged from 4 to 21 ml/day/nauplius stage IV to 286 ml to 773 ml/day/female. Ingestion rates increased from 0.2 g to 0.8 g C/day/nauplius stage IV to 18 g to 69 g C/day/female. Grazing and ingestion rates per unit body weight decreased gradually with increasing body weight. The daily ingested amount of food decreased from 292 to 481% of the body weight (g C) of nauplius stage V to 28–85% of the body weight of adult females. Grazing and ingestion performances of all stages increased with increasing particle size. Grazing rates decreased and ingestion rates increased with increasing food concentrations. The published data on food intake of the different age groups of C. helgolandicus show that the young stages of herbivorous planktonic copepods can play a major part in the consumption of phytoplankton in the sea due to their high grazing and ingestion rates.     

Influence of three sediment types on copper toxicity to the polychaete Neanthes arenaceodentata

Adult male Neanthes arenaceodentata were exposed to 0.10±0.015 mg l^-1 copper in the seawater of a continuous-flow bioassay system in the presence of a sand, a mud, a mixture of the sand and mud, and no sediment, to assess the influence of sediment type on Cu-induced mortality. The sediment type did influence mortality. The time to 50% mortality was 7.8 days without sediment, 36.5 days with sand, 54.5 days with the mixture, and 50.0 days with mud. There was no threshold Cu body burden that caused death. The mean Cu concentration per gram of N. arenaceodentata (24 h after death) without sediment was 270 g, in sand 994 g, in the mixture 1047 g, and in mud 1464 g. The differences in the toxic responses are discussed.     

Développement larvaire de deux Tellinacea,Scrobicularia plana (Semelidae) et Donax vittatus (Donacidae)

Scrobicularia plana Da Costa and Donax vittatus L. were reared in the laboratory through settlement. Fertilizable eggs were obtained by perfusing the ovary with 5% 0.1 M ammonium hydroxyde in sea water. S. plana eggs have a thick chorion, inside which the early larval stages develop; they hatch as straight-hinge larvae more than 60 h after fertilization. This brood protection is considered to be an adaptation to osmotic pressure changes and pollution in the environment. D. vittatus eggs have a very thin chorion and are unprotected. Further development is planktotrophic and very similar for the two species. Under laboratory conditions, the pediveliger stage is attained 3 weeks after fertilization and settlement occurs 1 week thereafter. S. plana spat stop growing until a suitable substratum is available. Meanwhile they undergo a byssus drifting important for postlarval dispersion. Post larvae resume growth as soon as a small quantity of fine sand is added to the rearing jar. The exhalant siphon is developed first, when the post larvae reach a length of 600 m; the inhalant siphon is formed later, at a length of approximately 900 m. Evolution from the larval hinge to the juvenile hinge stage occurs sooner in S. plana than in D. vittatus. Comparison of laboratory larval development with field development indicates that spawning occurs in June and August for S. plana in North Wales (UK).     

Effect of heavy metals (Zn,Hg, Cu,Cd, Pb,Ni) on the length growth of Mytilus edulis

The shortterm (10–22 d) effect of Zn, Hg, Cu, Cd, Pb, and Ni on the length growth of Mytilus edulis is studied. Significant reductions of growth rate was found at 0.3 g Hgl^-1, 3 g Cul^-1, 10 g Znl^-1, and 10 g Cdl^-1 added to the local sea water, while concentrations of up to 200 gl^-1 of Pb and Ni had no effect on the growth. With exposure to Cu and Zn, there was a linear reduction in growth rate with increasing metal concentration up to about 6 g Cul^-1 and 100 g Znl^-1. Above these levels, growth stopped with Cu, while with Zn it was stabilized at about 20% of control growth. When Hg and Cd were added, a curvilinear relationship between growth and metal concentration is indicated. With Hg, growth rate is nearly zero above 3–4 g Hgl^-1, while the growth rate was 50% of control after 10 d of exposure to 100 g Cdl^-1. At 2 g Cdl^-1 there was a significant stimulation of length increase. Observed EC₅₀-values for growth were 0.3–0.4 g Hgl^-1, 3–4 g Cul^-1, 60 g Znl^-1, and 100 g Cdl^-1.     

Inter-genotype aggression in the solitary sea anemone Actinia tenebrosa

The entire process of development from eggs to juveniles was observed in the sea-star Ctenopleura fisheri Hayashi. The breeding season of this sea-star in Toyama Bay, the Sea of Japan, occurs in the winter. The eggs are 465 in diameter, semitranslucent and pale brown in color. They develop into a barrel-shaped larva, neither bipinnaria nor brachiolaria, through a wrinkled blastula stage by holoblastic, radial cleavage. Larvae are free-swimming and do not feed during the larval stage. At metamorphosis the stalk, a larval organ, disappears by one of either 2 different processes; absorption into future body of the juveniles, or rupture and collapse. Fifteen days after insemination, metamorphosis is completed and the resulting juveniles, about 1 000 m in diameter, bear 2 pairs of tube-feet and a terminal tentacle in each arm.     

Effects of copper and cadmium on growth,swimming and predator avoidance in Eurytemora affinis (Copepoda)

In this study we demonstrate the sensitivity of swimming behavior and predator-escape responses of nauplii of the estuarine copepod Eurytemora affinis to sublethal doses of Cu and Cd. Behavior was generally altered at metal doses below those affecting growth rates or survival of the copepods. Swimming velocities of Cu-dosed nauplii were different from controls at all concentrations of Cu tested (10–50 g l^-1 total Cu) after 24- to 48-h exposure, whereas development rate of nauplii was significantly reduced only after 96 h at 25 g l^-1. The 96 h LC50 for Cu was approximately 30 g l^-1 Cu. Naupliar swimming velocity was also affected by Cd. Swimming speeds were reduced after 24 h at 130 g l^-1, and development was slowed after 48 h at 116 g Cd l^-1. The 96-h LC50 was >120 g l^-1. Little is known of the adaptive role of specific motile behaviors in the success of larval copepods. We investigated the relationship of swimming speed to predator — prey interactions of the nauplii using both real and simulated predators. Nauplii exposed to Cu for 24 h were observed to be generally hyperactive, a condition which could increase their encounter frequency with predators. Reduced numbers of escape responses of nauplii to a simulated predator, another indication of increased vulnerability to predation, were observed only after 48-h exposure to Cu. Nevertheless, feeding rates of non-dosed larval striped bass on dosed nauplii (24 h at 25 g Cu l^-1) were significantly higher than on control nauplii. Feeding rates of larval mysid shrimp, however, were not higher on similarly dosed nauplii; 24 h exposure of nauplii to >30 g Cu l^-1 did result in increased predation by mysids.Contribution No. 272 of the US EPA Environmental Research Laboratory, Narragansett, Rhode Island 02882, USA     

Nutrition studies in the nauplius larva of Calanus pacificus (Copepoda: Calanoida)

Nauplii of Calanus pacificus were raised on a mixture of algae. Details of the mouth-parts, such as denticles, labial palps and lobes, setations and structure of the masticatory teeth were examined by scanning electron microscopy (SEM). Under the experimental conditions (15°C and 300 gC l^-1), exponential growth coefficients for the period Nauplii II–VI were 0.179 for carbon and 0.228 for nitrogen. C:N ratios dropping from 5.1 to 4.7. Growth was isochronous, each stage lasting 1.5 days. Respiratory losses were 15 to 19.6% of body carbon daily. Nauplii raised on a given alga showed higher rates of ingestion in the presence of this food, compared to nauplii switched to other algae. Minimal threshold concentrations for feeding were found, depending on the size of the food offered and ranging from 5.8 gC I^-1 for Lauderia borealis (28.7 m spherical diameter) to 47.1 gC 1^-1 for Chlamydomonas sp. (11.0 m). Unlike the Copepodite I stage, Nauplii II–VI larvae were not able to ingest small cells such as Isochrysis galbana (4.3 m), or very large ones such as Ditylum brightwellii (47.5 m) at more than maintenance rations. Below the critical concentration for maximal feeding, ingestion was clearly dependent on size of the cells offered, but the size-dependent relationship was different for diatoms and non-diatoms. Filtering rates increased from a threshold concentration to a maximal rate at about 50 gC 1^-1, and decreased at higher concentrations. Critical concentrations ranged from 125 gC 1^-1 for L. borealis to 1000 gC 1^-1 for Chlamydomonas sp. Maximal daily rations ranged between 100 and 150% of body carbon.     

Relationship between phytoplankton cell size and the rate of orthophosphate uptake: in situ observations of an estuarine population

Orthophosphate uptake by a natural estuarine phytoplankton population was estimated using two methods: (1) ³²P uptake experiments in which filters of different pore sizes were used to separate plankton size-fractions; (2) ³³P autoradiography of phytoplankton cells. Results of the first method showed that plankton cells larger than 5 m were responsible for 2% of the total orthophosphate uptake rate. 98% of the total uptake rate occurred in plankton composed mostly of bacteria, which passed the 5 m screen and were retained by the 0.45 m pore-size filter. There was no orthophosphate absorption by particulates in a biologically inhibited control containing iodoacetic acid. Orthophosphate uptake rates of individual phytoplankton species were obtained using ³³P autoradiography. The sum of these individual rates was very close to the estimated rate of uptake by particulates larger than 5 m in the ³²P labelling experiment. Generally, smaller cells were found to have a faster uptake rate per m³ biomass than larger cells. Although the nannoplankton constituted only about 21% of the total algal biomass, the rate of phosphate uptake by the nannoplankton was 75% of the total phytoplankton uptake rate. Results of the plankton autoradiography showed that the phosphate uptake rate per unit biomass is a power function of the surface: volume ratio of a cell; the relationship is expressed by the equation Y=2x10^-11 X ^1.7, where Y is gP m^-3 h^-1 and X is the surface: volume ratio. These results lend support to the hypothesis that smaller cells have a competitive advantage by having faster nutrient uptake rates.     

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.     

Particle capture in the crown of the ciliary suspension feeding polychaete Sabella penicillus: videotape recordings and interpretations

An experimental setup was designed for in situ videotape recording of the particle capture process in the crown of the polychaete Sabella penicillus. Intact individuals of S. penicillus (collected in the Gullmornfjord, Sweden in 1992) were exposed to either 6 m Latex spheres or Rhodomonas sp. flagellate cells (6 m). The capture of the added particles was recorded on video. From frameby-frame analyses particle velocities were estimated and the shape of the three-dimensional particle paths was inferred. The mean velocity of particles approaching the crown was estimated to be ca. 1 mm s^-1, increasing to ca. 1.7 mm s^-1 in the interpinnule channel. At the moment of capture the particles were seen to follow a curved, near circular path close to the tips of the latero-frontal cilia. The transport velocities on the frontal side of the pinnules and filaments were estimated to be up to 0.15 and 0.5 mm s^-1, respectively. Counting captured particles relative to particles arriving within the area of the pinnules gave a rough, direct estimate of nearly 100% retention rate when the polychaete was feeding undisturbed. Together with results from clearance measurements in the literature this implies that the worm is able to capture particles down to 3 m entering the interpinnule channel almost 100% effectively. In view of the 80-m wide interpinnule channel and 40-m spacing between the tips of the latero-frontal cilia on both sides of the channel, this result cannot be explained by mechanisms based solely on direct mechanical contact between cilia and particles but must involve fluid mechanical mechanisms. The present work is the experimental basis for ongoing numerical simulations of the particle motion in the interpinnule channel.     

Development of the pericalymma larva of Solemya reidi (Bivalvia: Cryptodonta: Solemyidae) as revealed by light and electron microscopy

Solemya reidi Bernard 1980 is a gutless protobranch bivalve known to possess intracellular chemoautotrophic bacterial symbionts in its gill. A light and electron microscope study on the embryology and larval development of S. reidi provides data for the bivalve Subclass Cryptodonta. S. reidi spontaneously spawned large eggs (271 m in diameter), which developed within individual gelatious egg capsules. The first several cleavages were equal and a distinct molluscan cross was formed at the animal pole of the embryo, features previously unreported in bivalve development. Lecithotrophic pericalymma larvae (similar to the larvae of paleotaxodont protobranch bivalves and aplacophoran molluscs) hatched at 18 to 24 h and remained in the water column for a further 5 d at 10°C. At hatching, larvae measured from 360 to 440 m in length and from 225 to 265 m in cross-sectional diameter. Definitive adult structures developed within an epithelial locomotory test entirely covered with compound cilia. The test histolysed at metamorphosis and was ingested throught the mouth into the perivisceral cavity. Length and height of the shell following metamorphosis was 433 m (±42 m, n=16) and 282 m (± 29 m, n=13), respectively. Primary data and data from the literature show that the type of larval development in both paleotaxodont and cryptodont bivalves cannot be reliably estimated from egg or prodissoconch sizes.     

Potential effects of a resuspension event on the vertical distribution of copepod eggs in the sea bed: a laboratory simulation

Adult female Acartia tonsa and Labidocera aestiva were obtained from inshore marine waters near Turkey Point, Florida (29°54.5N;84°31W) during April and May 1991. For each species, eggs spawned overnight in the laboratory were collected, mixed with sediment, and added to a plastic tube (26 to 29 cm longx5 cm diam) to yield a 2 cm-thick layer. This tube was connected to a 245 cm-long tube, seawater was added and the contents were thoroughly mixed by turning the assembly end-over-end several times. The vertical distribution of eggs in the sediments following resuspension varied according to the grain size of the sediments. For sediments of 125 m particle-diameter, 68 to 72%, and 70 to 73% of the eggs of A. tonsa and L. aestiva, respectively, occurred in the upper 4 mm.For sediments 63 to <125 m particle-diameter, 34 to 36% of the eggs of A. tonsa and L. aestiva, respectively, occurred in the upper 4 mm. For sediments of <63 m particle-diameter, egg distribution was uniform for both species throughout the 2 cm layer. The results indicate that the vertical distribution of eggs in the sea bed following a resuspension event should be highly dependent upon the grain-size composition of the sediments.     

Toxicity of the fungicide captan to the Dungeness crab Cancer magister

Captan did not affect the survival of Dungeness crab (Cancer magister Dana) zoea exposed to 30 g l^-1 during a chronic toxicity test lasting 69 days, but larvae were quickly killed (mean survival time = 9 days) in the same test by exposure to 450 g l^-1 of the fungicide. Delay of molting occurred, however, for later stages at 30 g l^-1. Survival of juvenile crabs was not reduced by exposure to captan for 36 days at 510 g l^-1 or, in a second test, for 80 days at 290 g l^-1. No deaths of adults exposed for 75 days to 340 g l^-1 of captan were observed. Captan appeared to accelerate hatching of eggs at all concentrations tested from 100 to 10,000 g l^-1. The development from prezoeae during a 24-h period was not inhibited by the fungicide, but at 3,300 and 10,00 g l^-1, the two highest concentrations tested, developing zoeae exhibited a morphological deformity and were largely inactive. Under the prevailing conditions in the toxicity tests, the half-life of captan was estimated to be from 23 to 54 h. Because of the relatively low toxicity of captan to crab stages and its high rate of degradation in sewater, it is suggested that the agricultural application of captan near marine waters is not likely to affect natural crab populations or crabs in laboratory culture. Further-more, the prophylactic use of captan as a fungicidal treatment for Lagenidium sp. in larval crab cultures is considered safe when used at recommended dosages.Technical Paper No. 4131, Oregon Agricultural Experiment Station.     

Light requirements for growth of six shade-acclimated Mediterranean macroalgae

Six mediterranean macroalgae were cultivated for more than 2 yr under shade culture conditions, after which light requirements for growth were investigated at 16±2°C. The saturation light levels for growth in the logarithmic phase were related to the bathymetric distribution of the algae on the shore. The eulittoral to supralittoral red alga Bangia atropurpurea was saturated at a photon fluence rate of 71 mol photons m^-2 s^-1, the upper sublittoral to eulittoral brown algae Scytosiphon lomentaria, Colpomenia peregrina and Kuckuckia spinosa and the sublittoral brown alga Stictyosiphon soriferus at 39 to 71 mol photons m^-2 s^-1, and the deep-water alga Choristocarpus tenellus at 19 mol photons m^-2 s^-1. The minimum light requirements for growth of B. atropurpurea and C. tenellus were determined by observing length increase for 56 d under limiting light conditions. The compensation and minimum irradiances required for growth of B. atropurpurea were 0.5 and 1 mol photons m^-2 s^-1 respectively. The corresponding values for C. tenellus were 0.15 to 0.28 and 0.5 mol photons m^-2 s^-1 respectively. C. tenellus was the siowest-growing species tested at saturating light conditions, but it grew faster than B. atropurpurea at 1 mol photons m^-2 s^-1. Both B. atropurpurea and C. tenellus were able to survive 56 d in darkness, but only the latter grew under darkness in the first 14 d.     

Carotenoids versus retinoids (Vitamin A) as essential growth factors in penaeid prawns (Penaeus semisulcatus)

Penaeus semisulcatus de Haan adult gravid females, eggs and non-feeding early larvae, including Protozoea I, were used to test the hypothesis that retinoid (Vitamin A) is not required in early decapod crustacean development. In the adult gravid females, retinoids were detected only in the eyes (1.56±0.23 g g^-1 wet mass), whereas there were up to 97 g g^-1 wet mass total carotenoid in digestive gland and epidermis. This was mostly esterified, except in the ovaries, where free astaxanthin predominated (30 g g^-1). No retinoids could be detected in the eggs, the naupliar stages or Protozoea I, but free astaxanthin was metabolised exponentially, falling from 19 g g^-1 in the eggs to 4 g g^-1 in Protozoea I. This suggests that retinoid is not essential in early development and that carotenoid could be taking its place. Also, including retinoids in artificial diets appears to be unnecessary, provided adequate carotenoid is supplied.     

Time-dependent shifts between infanticidal and parental behavior in female burying beetles a mechanism of indirect mother-offspring recognition

Summary Female burying beetles Necrophorus vespilloides Herbst (Coleoptera: Silphidae) were allowed to lay eggs on a carcass and their subsequent behavior towards larvae added to the carcass was observed. Females did not discriminate against unrelated larvae if these were added within an hour after the females' own first larva had hatched (at the right time). Changing the spatial surroundings of the carcass had no effect on the females' readiness to exhibit care behavior. Neither did the age of the larvae added or the condition of the carcass affect the onset of maternal care. However, the females' response to larvae encountered was strongly time-dependent: most females killed and ate larvae that could not have hatched from their own eggs because they were added long before their own larvae hatched. The proportion of females accepting larvae added to early increased as the time their own larvae hatched approached. Larvae added to the carcass 2 or 3 days after the test females' own first larva had hatched were always accepted by females that had already started to feed larvae, but were often killed by females that were not feeding larvae. In the latter group of females, the tendency to kill larvae added was most pronounced if the females had already started to produce a second clutch of eggs at the time larvae were added. Offprint requests to: J.K. Müller