Knowledge of aquaculture–environment interactions is essential for the development of a sustainable aquaculture industry and efficient marine spatial planning. The effects of fish and shellfish farming on sessile wild populations, particularly infauna, have been studied intensively. Mobile fauna, including crustaceans, fish, birds and marine mammals, also interact with aquaculture operations, but the interactions are more complex and these animals may be attracted to (attraction) or show an aversion to (repulsion) farm operations with various degrees of effects. This review outlines the main mechanisms and effects of attraction and repulsion of wild animals to/from marine finfish cage and bivalve aquaculture, with a focus on effects on fisheries‐related species. Effects considered in this review include those related to the provision of physical structure (farm infrastructure acting as fish aggregating devices (FADs) or artificial reefs (ARs), the provision of food (e.g. farmed animals, waste feed and faeces, fouling organisms associated with farm structures) and some farm activities (e.g. boating, cleaning). The reviews show that the distribution of mobile organisms associated with farming structures varies over various spatial (vertical and horizontal) and temporal scales (season, feeding time, day/night period). Attraction/repulsion mechanisms have a variety of direct and indirect effects on wild organisms at the level of individuals and populations and may have implication for the management of fisheries species and the ecosystem in the context of marine spatial planning. This review revealed considerable uncertainties regarding the long‐term and ecosystem‐wide consequences of these interactions. The use of modelling may help better understand consequences, but long‐term studies are necessary to better elucidate effects.

No abstract

Current conventional wisdom argues that human-induced excesses in nutrient loadings to estuaries often stimulate 'excess' algal production leading to hypoxia, via bacterial pathways, and subsequent reduced recruitment/survival of finfish and shellfish. Why wouldn't such elevated production stimulate more animal production, rather than less? In a three-year study of Long Island Sound, U.S.A., a multitude of variables were quantified along a west to east gradient, to address the above question via the hypothesis that different successes among planktonic species experiencing eutrophication alter planktonic food web structure away from traditional pathways to microbial loop dominated ones. Variables studied included: nutrient concentrations and ratios (i.e. N02, N03, NH4, DON, PON, P04, Silicate, NIP and N/Si), phytoplankton, protozooplanktonic ciliate, zooplankton, heterotrophic nanoplankton (HNAN), photosynthetic nanoplankton (PNAN), size-fractionated chlorophyll, larval fish and bacterial concentrations and/or species composition, and bacterial growth rates (as frequency of dividing cells, FDC). Results indicated that although current nitrogen and other nutrient loadings into the estuary are much higher than past inputs (especially in western waters), the average concentration of dissolved inorganic nutrients is similar (though slightly higher) to past values. Relative proportioning among chemical species does vary from west to east, with NH4 and dissolved organic nitrogen (DON) at times more prevalent in the west, especially in bottom waters. Excess loadings of nitrogen and other nutrients into the estuary are converted to elevated biomass of both small ( < I 0 f.Lm), and large (>20 f.Lm) phytoplankton in the west. Slightly enhanced bacterial densities and growth rates shadow the elevated chlorophyll levels, with distinctive Sound-wide seasonal patterns that follow not total chlorophyll, but rather PNAN concentrations. HNAN concentrations also are elevated in the west, and likely influence bacterial dynamics. Species composition of phytoplankton routinely differ west to east. Inorganic NIP are routinely low (i.e. below Redfield ratios), especially in the west, while total dissolved N/P (i.e. including DON) are similar among stations and typically are significantly higher than Redfield ratios. Associated with bacterial and < 10 f.Lm chlorophyll enhancements to an elevated diversity of ciliate species in the west. Copepod biomass is extremely enhanced in the west, indicating that while stimulating the microbial loop, eutrophication is also enhancing the secondary production preferred by larval fish and gelatinous zooplankton. Larval fish diversity is down relative to the past, but shows little contemporaneous west/east variations. So, if adult fish populations are down, but larvae are not food limited, possibly toxicity, overfishing, and/or habitat destruction which prevent a healthy, normal system response to eutrophication are culpable. It is suggested that recipients of the excess copepod production are ...

The harmful dinoflagellate Prorocentrum minimum has different effects upon various species of grazing bivalves, and these effects also vary with life-history stage.Possible effects of this dinoflagellate upon mussels have not been reported; therefore, experiments exposing adult blue mussels, Mytilus edulis, to P. minimum were conducted. Mussels were exposed to cultures of toxic P. minimum or benign Rhodomonas sp. in glass aquaria. After a short period of acclimation, samples were collected on day 0 (before the exposure) and after 3, 6, and 9 days of continuousexposure experiment. Hemolymph was extracted for flow-cytometric analyses of hemocyte, immune-response functions, and soft tissues were excised for histopathology.Mussels responded to P. minimum exposure with diapedesis of hemocytes into the intestine, presumably to isolate P. minimum cells within the gut, thereby minimizing damage to other tissues. This immune response appeared to have been sustained throughout the 9-day exposure period, as circulating hemocytes retained hematological and functional properties. Bacteria proliferated in the intestines of the P. minimumexposed mussels. Hemocytes within the intestine appeared to be either overwhelmed by the large number of bacteria or fully occupied in the encapsulating response to P. minimum cells; when hemocytes reached the intestine lumina, they underwent apoptosis and bacterial degradation. This experiment demonstrated that M. edulis is affected by ingestion of toxic P. minimum; however, the specific responses observed in the blue mussel differed from those reported for other bivalve species. This finding highlights the need to study effects of HABs on different bivalve species, rather than inferring that results from one species reflect the exposure responses of all bivalves.

Excess nutrients in the coastal environment have been linked to a host of environmental problems, and nitrogen reduction efforts have been a top priority of resource managers for decades. The use of shellfish for coastal nitrogen remediation has been proposed, but formal incorporation into nitrogen management programs is lagging. Including shellfish aquaculture in existing nitrogen management programs makes sense from environmental, economic, and social perspectives, but challenges must be overcome for large-scale implementation to be possible.

The harmful dinoflagellate Prorocentrum minimum has different effects upon various species of grazing bivalves, and these effects also vary with life-history stage.Possible effects of this dinoflagellate upon mussels have not been reported; therefore, experiments exposing adult blue mussels, Mytilus edulis, to P. minimum were conducted. Mussels were exposed to cultures of toxic P. minimum or benign Rhodomonas sp. in glass aquaria. After a short period of acclimation, samples were collected on day 0 (before the exposure) and after 3, 6, and 9 days of continuousexposure experiment. Hemolymph was extracted for flow-cytometric analyses of hemocyte, immune-response functions, and soft tissues were excised for histopathology.Mussels responded to P. minimum exposure with diapedesis of hemocytes into the intestine, presumably to isolate P. minimum cells within the gut, thereby minimizing damage to other tissues. This immune response appeared to have been sustained throughout the 9-day exposure period, as circulating hemocytes retained hematological and functional properties. Bacteria proliferated in the intestines of the P. minimumexposed mussels. Hemocytes within the intestine appeared to be either overwhelmed by the large number of bacteria or fully occupied in the encapsulating response to P. minimum cells; when hemocytes reached the intestine lumina, they underwent apoptosis and bacterial degradation. This experiment demonstrated that M. edulis is affected by ingestion of toxic P. minimum; however, the specific responses observed in the blue mussel differed from those reported for other bivalve species. This finding highlights the need to study effects of HABs on different bivalve species, rather than inferring that results from one species reflect the exposure responses of all bivalves.

Harmful algal blooms (HABs) can have both lethal and sublethal impacts on shellfish. To understand the possible roles of haemocytes in bivalve immune responses to HABs and how the algae are affected by these cells (haemocytes), in vitro tests between cultured harmful algal species and haemocytes of the northern quahog (= hard clam) Mercenaria mercenaria, the soft-shell clam Mya arenaria, the eastern and Pacific oysters Crassostrea virginica and Crassostrea gigas and the Manila clam Ruditapes philippinarum were carried out. Within their respective ranges of distribution, these shellfish species can experience blooms of several HAB species, including Prorocentrum minimum, Heterosigma akashiwo, Alexandrium fundyense, Alexandrium minutum and Karenia spp.; thus, these algal species were chosen for testing. Possible differences in haemocyte variables attributable to harmful algae and also effects of haemolymph and haemocytes on the algae themselves were measured. Using microscopic and flow cytometric observations, changes were measured in haemocytes, including cell morphology, mortality, phagocytosis, adhesion and reactive oxygen species (ROS) production, as well as changes in the physiology and the characteristics of the algal cells, including mortality, size, internal complexity and chlorophyll fluorescence. These experiments suggest different effects of the several species of harmful algae upon bivalve haemocytes. Some harmful algae act as immunostimulants, whereas others are immunosuppressive. P. minimum appears to activate haemocytes, but the other harmful algal species tested seem to cause a suppression of immune functions, generally consisting of decreases in phagocytosis, production of ROS and cell adhesion and besides cause an increase in the percentage of dead haemocytes, which could be attributable to the action of chemical toxins. Microalgal cells exposed to shellfish haemolymph generally showed evidence of algal degradation, e.g. loss of chlorophyll fluorescence and modification of cell shape. Thus, in vitro tests allow a better understanding of the role of the haemocytes and the haemolymph in the defence mechanisms protecting molluscan shellfish from harmful algal cells and could also be further developed to estimate the effects of HABs on bivalve molluscs in vivo.

The possible effect of Alexandrium spp. containing paralytic shellfish poisoning (PSP) toxins on the hemocyte parameters of oysters was tested experimentally. In separate experiments, eastern oysters, Crassostrea virginica, were exposed to bloom concentrations of the sympatric dinoflagellate, Alexandrium fundyense, alone and in a mixture with a non-toxic diatom, Thalassiosira weissflogii, and Pacific oysters, Crassostrea gigas, were exposed to a mixed suspension of the sympatric, toxic species Alexandrium catenella, with T. weissflogii. Measurements of numbers of oyster hemocytes, percentages of different cell types, and functions (phagocytosis, reactive oxygen species-ROS-production, and mortality) were made using flow-cytometric methods. During and after exposure, no significant effect of Alexandrium upon hemocyte numbers, morphology, or functions were detected, despite observations of adductor-muscle paralysis in eastern oysters and measured toxin accumulation in C. gigas. Significant effects of physical displacement of oysters into the experimental conditions and of temperature (repeated at 12 and 18°C) upon immune status were detected in Pacific oysters. Correlations between hemocyte numbers and function were consistent with previous studies and were representative of normal, unstressed oysters. The finding of no effect of toxic Alexandrium spp. upon oyster hemocytes is consistent with the knowledge that PSP toxins interfere specifically with sodium-channel function in neural tissues and supports the expectation that sodium-channel physiology has no importance in hemocyte functions in oysters. Finally, we found no evidence of bioactive compounds, other than PST, in the two species of Alexandrium studied.