Journal of the Marine Biological Association of the United Kingdom最新文献

The reproductive cycle of Marphysa sanguinea is described for a population at Mount Edgecombe, Plymouth, near the type location in Southwest England, using a data set obtained previously (October 1999 to September 2000). The species is iteroparous without schizogamy, spawning prior to October 1999 and during a short breeding season in 2000 from end August through September. The sexes are separate with a sex ratio of 1:1. Mature oocytes and spawned eggs are 215 μm in diameter and spermatozoa of the ectaqua sperm type. Mature gametes of both sexes are discharged through paired coelomoducts, and the diploid chromosome number is 28. Proliferation of new coelomic gametes from paired gonads began within a month of spawning and continued for 8–9 months but ovulation was suppressed in June and July. Attempts to undertake fertilisation using spawned oocytes and active spermatozoa were unsuccessful. The size of discharged oocytes suggests a short pelagic larval duration of a few days. This is the first publication about the reproduction of this species, and our results suggest that M. sanguinea is restricted to intertidal areas in SW England, NW France and southern North Sea. The highly synchronised pattern of reproduction observed is not compatible with a quasi-cosmopolitan species range indicating that this species has been mistakenly reported from around the world. Future studies of the genus should combine rigorous taxonomy with observations of reproduction to facilitate comparison among Marphysa spp.

In the present study, 15 new records from Kavaratti Atoll are added to the ichthyofaunal diversity of the Lakshadweep Archipelago and six to the Indian fish fauna based on underwater photographs and videos. Fishes were recorded from both lagoon and forereef areas off Kavaratti. The new records include Cirripectes auritus (Blackflap blenny), Cirripectes polyzona (Barred blenny), Ecsenius bicolor (Bicolor blenny), Glyptoparus delicatulus (Delicate blenny), Amblyeleotris wheeleri (Gorgeous prawn-goby), Eviota punyit (Punyit dwarfgoby), Eviota cf. teresae (Viridescent dwarfgoby), Cirrhitichthys falco (Dwarf hawkfish), Halichoeres leucoxanthus (Canarytop wrasse), Pseudocheilinus evanidus (Disappearing wrasse), Coris latifasciata (Broad banded wrasse), Pomacentrus xanthocercus (Yellowtail damsel), Plectroglyphidodon luteobrunneus (Indian gregory), Pomacentrus indicus (Indian damsel) and Synodus dermatogenys (Sand lizardfish). Six species, G. delicatulus, E. cf. teresae, E. punyit, P. xanthocercus, P. evanidus and C. latifasciata represent new records for Indian waters. The genus Amblyeleotris is recorded for the first time from Lakshadweep.

Bobtail squids (Family Sepiolidae) have a variety of sperm storage patterns, but their reproductive biology has not been studied in many species, especially those in Japanese waters. Two species, Austrorossia bipapillata (Subfamily Rossiinae) and Sepiolina nipponensis (Subfamily Heteroteuthinae) inhabit Suruga Bay in Japan. These were sampled approximately bimonthly by trawling at around 500 m between the end of September, 2020 and May, 2022. They were measured for body size (dorsal mantle length) and weighed for gonadosomatic index (GSI) calculation, and their sperm storage mechanism was investigated. The reproductive season occurs from May to October in A. bipapillata and from December to February in S. nipponensis. In both species, spermatangia were deposited inside the mantle cavity as implanted spermatangia. In A. bipapillata, 5.7 ± 6.5 spermatangia were deeply implanted in the opening of the oviduct, and in S. nipponensis 62.7 ± 61.5 spermatangia were attached to the left gill and surface of the connective-tissue capsule enclosing the digestive gland. The GSI was lower and there were fewer spermatophores stored in the spermatophoric sac of A. bipapillata males compared to S. nipponensis, leading us to suggest that it is exposed to weaker sperm competition than S. nipponensis, irrespective of similar sperm storage mechanism in the two species.

Entanglement in static fishing gear is the largest cause of non-natural mortality for minke whales (Balaenoptera acutorostrata) in Scottish waters. To mitigate whale entanglement, one priority is to identify areas where the risk of entanglement is consistently high. Sightings data for minke whales and creel fleets were collected by the Hebridean Whale and Dolphin Trust, during vessel line transect surveys conducted between 2008 and 2014. Habitat modelling was used to relate survey, environmental, and temporal variables to the co-occurrence of minke whales and creels in coastal waters of western Scotland. This revealed that minke whale occurrence was related to depth, peaking around 70 m. Using predictive habitat modelling, the overlap between minke whale habitat and the creel fishery was measured as risk of entanglement. A method was developed to quantify the consistency of risk over the seven-year time period. This allowed for the identification of areas where there had been a consistently low, medium, or high risk of entanglement from 2008 to 2014. The three areas with a consistent high risk of entanglement were identified: Inner Sound and Sound of Raasay, east of North and South Uist, and north of The Small Isles. The method presented here could be used to guide management to areas where mitigation efforts will be the most consistently effective over time.

Pseudechinus magellanicus is an ecologically important and small sea urchin in coastal and nearshore habitats off southern South America. We provide the first growth assessment for the species using tag (calcein) and recapture procedures in central Patagonia (Argentina). The individual growth rate of P. magellanicus ranged 0.05–1.3 mm year−1. The Brody–Bertalanffy and Richards growth models provided asymptotic maximum diameters of 29.89 and 26.01 mm, respectively. Both models yielded low values for the growth constant (k), with 0.046 (Brody–Bertalanffy) and 0.062 (Richards). Maximum instantaneous growth rate was estimated at 1.36 mm year−1 for the Brody–Bertalanffy model, and 2.69 mm year−1 for the Richards model. Model selection (corrected Akaike information criterion) showed a slight better fit for the Brody–Bertalanffy growth model compared to the Richards model. A significant variability in growth was observed within the studied population, which can be attributed to genetic factors and micro-environmental effects. P. magellanicus displays a combination of slow growth and small body size, with the lowest recorded growth performance index (θ = 3.72) recorded so far in sea urchins. The species has a long lifespan, with the most common adult sizes estimated to range from 15 to 21 years according to the Brody–Bertalanffy model. Due to the broad geographic distribution and occupation of contrasting habitats, further studies are necessary to explore growth of P. magellanicus under different environmental conditions and/or along a bathymetric gradient.