Larval habitat choice in still water and flume flows by the opportunistic bivalve Mulinia lateralis
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Point pattern analysis as a tool for assessing disease spread and population features in remaining sanctuaries of the critically endangered bivalve Pinna nobilis
2022, Journal for Nature ConservationCitation Excerpt :Their presence explains the distribution of pen shells along belt areas parallel to shore and the tendency towards disperse patterns at larger scales in all zones. Compared to other bivalves where clustering in dense matts or reefs are the result of selective settlement patterns (Grassle et al., 1992; Vasquez et al., 2013), those of the pen shell appear to be due to an early life-stage strategy based on low buoyancy and passive drift. The possible effect of parental detection in larval settlement cannot be fully discarded, but there was considerable variability in mean NN distances to another shell across zones (from only 1.2 in the Banya to 3.1 m in the St. Joan Tower), which suggest that adult proximity is not a necessary requirement.
Reproduction
2017, Developments in Aquaculture and Fisheries ScienceEffects of settlement cues on behaviour and substrate attachment of hatchery reared winged pearl oyster (Pteria penguin) larvae
2012, AquacultureCitation Excerpt :The presence of a microbial bio-film on the surface of substrata has been found to promote settlement in a number of commercial bivalve taxa including scallops (Leyton and Riquelme, 2008; Parsons et al., 1993), mussels (Bao et al., 2007), oysters (Anderson, 1996; Tamburri et al., 1992; Walch et al., 1987) and pearl oysters (Su et al., 2007; Yu et al., 2010; Zhao et al., 2003). The response of larvae to the presence of a bio-film depends on whether the cues are water-borne or surface-bound signals (Wieczorek and Todd, 1998) and the ability of larvae to detect and actively swim towards the origin of those cues (Grassle et al., 1992; Tamburri et al., 1992; Wieczorek and Todd, 1998). Molluscs show a high degree of substratum chemical specificity (Hadfield, 1984), explaining why microbial community structure, as opposed to microbial abundance, is thought to be the primary determinant of bio-film efficacy at inducing settlement of some bivalve species (Yu et al., 2010).
Effects of current speed, shell length and type of sediment on the erosion and transport of juvenile softshell clams (Mya arenaria)
2007, Journal of Experimental Marine Biology and EcologyRecolonization of defaunated sediments: Fine versus gross sand and dredging versus experimental trays
2006, Estuarine, Coastal and Shelf ScienceCitation Excerpt :To study the relationships between benthic communities and their environment, different approaches can be used (Wu and Shin, 1997). One approach involves experimental testing of larval settlement in different sediments (e.g. Grassle et al., 1992) and a second approach utilizes comparisons of field distributions of macrofaunal assemblages to sediment characteristics (e.g. Etter and Grassle, 1992). As pointed out by Wu and Shin (1997), the problem with the first approach is in extrapolating simplified, controlled laboratory results to complex, dynamic field conditions and scaling up small-scale experiments to ecologically meaningful spatial scales (Thrush et al., 1997).
Spatial and temporal variation in surfclam (Spisula solidissima) larval supply and settlement on the New Jersey inner shelf during summer upwelling and downwelling
2005, Estuarine, Coastal and Shelf ScienceCitation Excerpt :The role of active larval habitat selection in establishing initial settlement patterns has long been recognised (review by Butman, 1987). Recent flume and field studies indicate that near-bottom hydrodynamics also play an important role in larval settlement of soft-sediment invertebrates (e.g. Grassle et al., 1992; Snelgrove, 1994). On larger scales (relative to processes in the bottom boundary layer), physical circulation affects larval distribution.