Fisheries and Oceans Canada / Pêches et Océans Canada - Government of Canada / Gouvernement du Canada
 
Fisheries and Oceans Canada

A SCIENTIFIC REVIEW OF THE POTENTIAL ENVIRONMENTAL EFFECTS OF AQUACULTURE IN AQUATIC ECOSYSTEMS - VOLUME 1

Table of Contents

FAR-FIELD ENVIRONMENTAL EFFECTS  OF MARINE FINFISH AQUACULTURE

B.T. Hargrave

Marine Environmental Sciences, Fisheries and Oceans Canada
Bedford Institute of Oceanography, Dartmouth, Nova Scotia

 

EXECUTIVE SUMMARY

This review evaluates the existing knowledge and research needs required to determine the ability of coastal waters to support a sustainable marine finfish aquaculture industry. A central question is what methods, environmental observations and models exist, or are required, to determine the capacity of coastal areas to assimilate additional sources of dissolved and particulate matter released by cultured finfish.

Pillay (1992) provided an early review of major environmental effects of all types of aquaculture on a worldwide basis. Over the past decade, several international groups have considered various environmental issues surrounding the development of marine finfish aquaculture (Rosenthal 1988, 1994; GESAMP 1991, 1996; Buerkly 1993; Stewart et al. 1993; Ervik et al. 1994a, 1997; Stewart 1994, 2001; Rosenthal et al. 1995; Silvert and Hargrave 1995; Burd 1997; Goldberg and Triplett 1997; Milewski et al. 1997; Fernandes et al. 2000; Harvey 2000; Milewski 2000; EVS 2001; Holmer et al. 2001). Much of the information on environment-finfish aquaculture interactions in publications cited above is focused on measurable near-field changes in water and sediment variables sensitive to organic matter and nutrient additions.

Despite the difficulties of observing far-field effects, published literature shows that in some locations, measurable effects attributable to finfish aquaculture development have been observed at the ecosystem level. The impacts may be categorized into three types of broad-scale changes distant from farm sites: eutrophication, sedimentation and effects on the food web.

It is a common observation that the amount of suspended particulate matter increases in the immediate vicinity of finfish net-pens. When feed pellets are distributed by hand or automatic mechanical feeders, a fine dust may potentially be transported in the air or trapped in the water surface film and spread over a broad area. Unconsumed feed pellets and fish feces usually contribute to increased local concentrations of suspended and sedimented particulate matter. While much of the released material is assumed to settle rapidly at or near cage sites (Gowen et al. 1994; Silvert 1994e; Findlay et al. 1995; Findlay and Watling 1997), there is potential for horizontal transport and widespread dispersion, particularly in areas with high currents (Sutherland et al. 2001; Cromey et al. 2002). Holmer (1991) collected material, directly attributable to a finfish aquaculture source, at distances up to 1.2 km from a farm site in Danish coastal water. The extent to which resuspension and lateral transport increase sedimentation at locations remote from farm sites depends on both physical and sedimentological processes. Tidal flow, residual circulation, patterns of turbulence, wind and wave energy, and flocculation (aggregation) will determine large-scale patterns of particle dispersion. The distances and locations of accumulation are highly site-specific and depend on bottom topography, currents, erosion and flocculation processes that affect the residence time of material both in the column (Sutherland et al. 2001) and on the bottom (Milligan and Loring 1997).

Specific compounds associated with organic matter, such as fatty acids, digestible proteins, sterols, elemental sulfur, pristane and stable carbon/nitrogen isotopes (Li-Xun et al. 1991; Johnsen et al. 1993; Findlay et al. 1995; McGhie et al. 2000) and trace elements such as zinc that might be used as tracers of fish feed pellets, have been measured in surface sediments to determine far-field dispersion patterns (Ye et al. 1991; McGhie et al. 2000; Sutherland et al. 2002; Yeats 2002). Alteration of bottom type to more fine-grained sediments through enhanced deposition of flocculated, fine-grained material may also account for the speculation that a population of lobsters was displaced from their historic spawning ground after a salmon farm was located at the site (Lawton and Robichaud 1991). However, an opposite effect of salmon farm operations causing aggregations of lobster may also occur. Salmon farm sites may be a refuge for lobsters from harvesting.

Eutrophication is the process of natural or anthropogenic enrichment of aquatic systems with inorganic nutrient elements (Jørgensen and Richardson 1996; Strain and Yeats 1999; Cloern 2001). Long-term eutrophication of coastal and estuarine waters results from the additions of both dissolved inorganic and organic nutrients and increased biological oxygen demand (BOD) from oxygen-consuming material from all sources (Rosenberg 1985; Costa-Pierce 1996; Johannessen and Dahl 1996; Cloern 2001). Dissolved inorganic nutrients released by finfish culture and regenerated from sediments enriched with sedimented organic matter under fish pens may stimulate phytoplankton production and increase oxygen demand. It is often difficult to accurately estimate the magnitude of additions of nutrients and organic matter from finfish aquaculture when many environmental factors and possible sources of addition occur (Einen et al. 1995; Strain et al. 1995). Models can help determine the relative amounts of organic loading from aquaculture from all natural sources (river discharge, tidal exchange, rainfall, phytoplankton and macroalgal production) and human inputs (Valiela et al. 1997). The degree of nutrient enrichment is influenced by the scale of aquaculture, local hydrographic characteristics, the magnitude of other sources relative to aquaculture and internal processes, such as uptake by phytoplankton, algae, internal recycling, resuspension of fine material, and uptake by biofouling communities that colonize net- pens.

The effects of eutrophication may extend into shallow water littoral and intertidal zones. Intertidal areas, subject to daily movements of water and sediment, are locations influenced by broad-scale processes affecting chemical fluxes of mass and dissolved material throughout an inlet system. Nutrient enrichment can stimulate the extensive development of macroalgal beds (Soulsby et al. 1982; Petrell et al. 1993; Campbell 2001), which have a large capacity for nutrient uptake (Chopin and Yarish 1999; Chopin et al. 2000) and may affect benthic fauna through changes in the rates and nature of deposition of particulate organic matter (Bourget et al. 1994). However, few studies have unequivocally linked the establishment of aquaculture farm sites to environmental or ecological changes in intertidal areas.

Eutrophication can alter the ratio between essential nutrients (carbon: nitrogen:phosphorus), as well as absolute concentrations by causing a shift in phytoplankton species assemblages. It has proven difficult to directly relate the occurrence of harmful algal blooms (HAB) to finfish farms. As with other types of plankton blooms, many environmental factors appear to control the formation of HABs. Water column mixing and stratification that maintain cells in the photic zone with an adequate nutrient supply are critical variables. In contrast to numerous studies of localized benthic effects of finfish aquaculture at farm sites, there have been very few observations of effects on plankton communities (Burd 1997). Reductions in zooplankton standing stock with oxygen depletion could allow standing stocks of phytoplankton to increase. With sufficient nutrient and light supplies, higher rates of primary production and increased sedimentation would result in even further oxygen depletion in deep water.

There is an extensive literature documenting changes in benthic infauna community structure associated with high levels of nutrient and organic matter additions (Burd 1997). Only fauna (e.g. nematodes and polychaetes) tolerant of low oxygen conditions and reduced sulfides are able to survive under conditions of high organic sedimentation (Hargrave et al. 1993, 1997; Duplisea and Hargrave 1996). The presence/absence of these 'indicator' species or faunal groups may show transitions from lower (background) levels of organic matter supply to high deposition rates caused by unconsumed feed pellets and fish feces in areas subject to low transport (Weston 1990; Pocklington et al. 1994; Burd 1997). Moderate increases in organic matter supply may stimulate macrofauna production and increase species diversity; however, with increasingly higher rates of organic input, diversity and biomass decrease.

Widespread changes in species community composition of benthic macrofauna distant from farm sites are more difficult to detect and have been less studied. Temporal and spatial scales of changes in benthic macrofauna species composition and biomass have been measured over the past decade in some areas as part of long-term monitoring programs near net-pens to determine if organic enrichment effects from aquaculture can be detected (Burd 1997; Brooks 2001). Most studies have shown that the local extent of altered benthic community structure and biomass is limited to  less than 50 m. Water depth and current velocity are critical factors determining patterns of sedimentation around cage sites (Weston 1990; Pohle et al. 1994; Silvert 1994e; Henderson and Ross 1995; Burd 1997; Pohle and Frost 1997; Brooks 2001; Cromey et al. 2002), and therefore impacts of benthic fauna differ at different farm sites. In southwest New Brunswick, organic enrichment effects at newly established farm sites were localized to within 30 m of cages. After approximately five years, changes were measurable over greater (>200 m) distances. Macrofaunal community diversity was most reduced close to a farm site that had been in operation for 12 years, but significant declines in diversity also occurred throughout the inlet system. Benthic epifauna and infauna at two intertidal sites at varying distances from aquaculture sites showed that the diversity of infauna was significantly higher away (>500 m) than near (<500 m) farm sites (Wong et al. 1999). Loss of diversity at distances less than 500 m may indicate that benthic infauna are more sensitive to organic matter additions than epifauna (Warwick 1986, 1987), possibly reflecting changes in sediment physical structure (grain size), oxygen supply and sulfide accumulation associated with increased organic matter supply.

Another far-field effect of local sources of organic matter produced by finfish farm sites involves the use of chemotherapeutants. Antibiotics in medicated fish feed have the potential to induce drug resistance in natural microbial populations on an inlet-wide scale. Concentrations of a commonly used antibiotic, oxytetracycline (OTC), largely disappeared within a few weeks, but traces of the antibiotic were detectable for up to 18 months (Samuelsen et al. 1992). In Puget Sound, the highest numbers of bacteria (as colony-forming units) in sediments generally occurred at farm sites (Herwig et al. 1997), but the proportion of OTC resistant bacteria declined exponentially with increasing distance from a farm. Ervik et al. (1994b) also observed antibiotics in fish and wild mussels near a farm site after medicated food had been administered, and OTC resistance has been observed in bacteria cultured from sediments up to 100 m away from salmon farm sites in inlets in the Bay of Fundy where salmon farms are concentrated (Friars and Armstrong 2002).

GAPS IN KNOWLEDGE

1.      There is a need to determine sustainable levels of salmon production within coastal regions, inlets or embayments where marine finfish aquaculture is currently practiced in Canada.

2.      Mass balance models of nutrient loading (inorganic and organic) from all sources (natural and anthropogenic) may be used to assess potential additions from finfish aquaculture. Budgets must take into account internal nutrient recycling as well as external sources.

3.      General circulation models can be developed and improved to resolve combined effects of tidal and wind-driven forcing and that reflect complex topography and intertidal drying zones.

4.      New methods are required to quantify processes of resuspension that redistribute fine material produced locally by finfish aquaculture sites over large areas.

5.      New methods are required to quantify processes, such as flocculation and aggregation, that affect dispersion of particulate matter from finfish farm sites.

6.      Studies are required to determine if the frequency and location of HAB or plankton blooms are related to the expansion of finfish aquaculture.

7.      New studies are required to determine changes in water column variables in areas of intensive finfish aquaculture. In comparison to benthic studies, there have been very few investigations of changes in planktonic communities around finfish aquaculture sites.

8.      Further studies are required to document environmental or ecological changes in intertidal areas and to determine if these can be linked unequivocally to the establishment of aquaculture sites.

9.      Mass balance and numerical models are required to link production and external loading with aerobic and anaerobic oxidation of organic matter (pelagic and benthic), sedimentation and sulfide accumulation in sediment.

10.  Further studies are required to determine the extent of far-field effects on ecological and biological impacts of antibiotic resistance induced in microbial and other wild populations in areas of intensive finfish aquaculture.

The complete papers can be found in the following document:

Fisheries and Oceans Canada. 2003. A scientific review of the potential environmental effects of aquaculture in aquatic ecosystems. Volume 1. Far-field environmental effects of marine finfish aquaculture (B.T. Hargrave); Ecosystem level effects of marine bivalve aquaculture (P. Cranford, M. Dowd, J. Grant, B. Hargrave and S. McGladdery); Chemical use in marine finfish aquaculture in Canada: a review of current practices and possible environmental effects (L.E. Burridge). Can. Tech. Rep. Fish. Aquat. Sci. 2450: ix + 131 p.

REFERENCES

Bourget, E., L. Lapointe, J.H. Himmelman and A. Cardinal. 1994. Influence of physical gradients on the structure of a northern rocky subtidal community. Ecoscience 1: 285-299.

Brooks, K.M. 2001. An evaluation of the relationship between salmon farm biomass, organic inputs to sediments, physicochemical changes associated with those inputs and the infaunal response – with emphasis on total sediment sulfides, total volatile solids, and oxidation-reduction potential as surrogate endpoints for biological monitoring. Report to the Technical Advisory Group, MLWP, Nanaimo, BC. (www.bcsalmonfarms.bc.ca/network/ publications. html).

Buerkly, B. 1993. The aquaculture industry in the Bay of Fundy. Conservation Council of New Brunswick, Occ. Papers Ser. 7: 1-17.

Burd, B. 1997. Salmon Aquaculture Review interim draft report. Key issue C: Waste discharges. BC Environmental Assessment Office, BC Department of Fisheries and Aquaculture, Victoria, BC. 157 p.

Campbell, S. 2001. Ammonium requirements of fast-growing ephemeral macroalgae in a nutrient-enriched marine embayment (Port Phillip Bay, Australia). Mar. Ecol. Prog. Ser. 209: 99-107.

Chopin, T. and C. Yarish. 1999. Nutrification in the Bay of Fundy: sustainable integrated aquaculture as one of the bioremediation tools, p. 39. In J. Ollerhead, P.W. Hicklin, P.G. Wells and K. Ramsey [eds.]. Understanding change in the Bay of Fundy ecosystem. Proc. 3rd Bay of Fundy Workshop. Environment Canada, Occ. Rep. 12.

Chopin, T., D. Welles and E. Belyea. 2000. Seaweeds, nutrients and aquaculture in coastal waters… let’s put things in perspective, p. 39. In R.W. Rangeley and J. Davies [eds.]. Gulf of Maine rockweed: management in the face of scientific uncertainty. Huntsman Marine Science Centre Occ. Rep. 00/1, St. Andrews, NB.

Cloern, J.E. 2001. Our evolving conceptual model of the coastal eutrophication problem. Mar. Ecol. Prog. Ser. 210: 223-253.

Costa-Pierce, B.A. 1996. Environmental impacts of nutrients from aquaculture: towards the evolution of sustainable aquaculture, p. 81-113. In D.J. Baird, M.C.M. Beveridge, L.A. Kelly and J.F. Muir [eds.]. Aquaculture and water resource management. Blackwell Science, U.K.

Cromey, C.J., T.D. Nickell and K.D. Black. 2002. DEPOMOD-modelling the deposition and biological effects of waste solids from marine cage farms. Aquaculture 214: 211-239.

Duplisea, D. and B.T. Hargrave. 1996. Response of meiobenthic size-structure, biomass and respiration to sediment organic enrichment. Hydrobiol. 339: 161-170.

Einen, O., I. Holmefjord, T. Asgard and C. Talbot. 1995. Auditing nutrient discharges from fish farms: theoretical and practical considerations. Aquac. Res. 26: 701-713.

Ervik, A., P. Kupka Hansen and V. Wennevik. 1994a. Proceedings of the Canada-Norway Workshop on Environmental Impacts of Aquaculture. Fisken Havet 13. 135 p.

Ervik, A., B. Thorsen, V. Eriksen, B.T. Lunestad, and O.B. Samuelsen. 1994b. Impact of administering antibacterial agents on wild fish and blue mussels Mytilus edulis in the vicinity of fish farms. Dis. Aquat. Org. 18: 45-51.

Ervik, A., P.K. Hansen, J. Aure, A. Stigebrandt, P. Johannessen and T. Jahnsen. 1997. Regulating the local environmental impact of intensive marine fish farming. I. The concept of the MOM system (Modelling-Ongrowing fish farms-Monitoring). Aquaculture 158: 85-94.

EVS Consultants. 2001. Impacts of freshwater and marine aquaculture on the environment: knowledge and gaps. Report to the Department of Fisheries and Oceans, Ottawa, ON.

Fernandes, T.F., K.L. Miller and P.A. Read. 2000. Monitoring and regulation of marine aquaculture in Europe. J. Appl. Ichthyol. 16: 138-143.

Findlay, R.H. and L. Watling. 1997. Prediction of benthic impact for salmon net-pens based on the balance of benthic oxygen supply and demand. Mar. Ecol. Prog. Ser. 155: 147-157.

Findlay, R.H., L. Watling and L.M. Mayer. 1995. Environmental impact of salmon net-pen culture on marine benthic communities in Maine. A case study. Estuaries 18: 145-179.

Friars, F. and S. Armstrong. 2002. The examination of possible oxytetracycline resistance in microbes isolated from sediments under and around finfish aquaculture sea cage sites in Southwestern New Brunswick, p. 79. In B.T.
Hargrave [ed.]. Environmental Studies for Sustainable Aquaculture (ESSA): 2002 workshop report. Can. Tech. Rep. Fish. Aquat. Sci. 2411: v + 117 p.

GESAMP (IMO/FAO/UNESCO/WMO/WHO/IAEA/UN/UNEP Joint Group of Experts on the Scientific Aspects of Marine Pollution). 1991. Reducing environmental impacts of coastal aquaculture. Rep. Stud. GESAMP No. 47, FAO, Rome, Italy. 35 p.

GESAMP (IMO/FAO/UNESCO/WMO/WHO/IAEA/UN/UNEP Joint Group of Experts on the Scientific Aspects of Marine Pollution). 1996. Monitoring the ecological effects of coastal aquaculture wastes. Rep. Stud. GESAMP No. 57, FAO, Rome, Italy. 38 p.

Goldberg, R. and T. Triplett. 1997. Murky waters: environmental effects of aquaculture in the U.S. Environmental Defense Fund, Washington, DC. 197 p.

Gowen, R.J., D. Smyth and W. Silvert. 1994. Modelling the spatial distribution and loading of organic fish farm waste to the seabed, p. 19-30. In B.T. Hargrave [ed.]. Modelling benthic impacts of organic enrichment from marine aquaculture. Can. Tech. Rep. Fish. Aquat. Sci. 1949: xi + 125 p.

Hargrave, B.T., D.E. Duplisea, E. Pfeiffer and D.J. Wildish. 1993. Seasonal changes in benthic fluxes of dissolved oxygen and ammonium associated with marine cultured Atlantic salmon. Mar. Ecol. Prog. Ser. 96: 249-257.

Hargrave, B.T., G.A. Phillips, L.I. Doucette, M.J. White, T.G. Milligan, D.J. Wildish and R.E. Cranston. 1997. Assessing benthic impacts of organic enrichment from marine aquaculture. Water, Air Soil Pollut. 99: 641-650.

Harvey, J. 2000. Aquaculture in southwestern New Brunswick: a question of sustainability. Brief to the House of Commons Standing Committee on Fisheries and Oceans, St. Andrews, NB (Oct. 16, 2000), Conservation Council of New Brunswick.

Henderson, A.R. and D.J. Ross. 1995. Use of macrobenthic infaunal communities in the monitoring and control of the impact of marine cage fish farming. Aquac. Res. 26: 659-678.

Herwig, R.P., J.P. Gray and D.P. Weston. 1997. Antibacterial resistant bacteria in surficial sediments near salmon net-cage farms in Puget Sound, Washington. Aquaculture 149: 263-283.

Holmer, M. 1991. Impacts of aquaculture on surrounding sediments: generation of organic-rich sediments, p. 155-175. In N. DePauw and J. Joyce [eds.]. Aquaculture and the environment. European Aquaculture Society Spec. Publ. 16, Ghent, Belgium.

Holmer, M., P. Lassus, J.E. Stewart and D.J. Wildish. 2001. ICES Symposium on environmental effects of mariculture. ICES J. Mar. Sci. 58: 363-368.

Johannessen, T. and E. Dahl. 1996. Declines in oxygen concentrations along the Norwegian Skagerrak coast, 1927-1993: a signal of ecosystem changes due to eutrophication. Limnol. Oceanogr. 41: 766-778.

Johnsen, R.I., O. Grahl-Nielsen and B.T. Lunestad. 1993. Environmental distribution of organic waste from a marine fish farm. Aquaculture 118: 229-244.

Jørgensen, B.B. and K. Richardson. 1996. Eutrophication in coastal marine ecosystems. Amer. Geophys. Union, Washington, D.C. 272 p.

Lawton, P. and D. Robichaud. 1991. Shallow water spawning and moulting areas of American lobsters, Homarus americanus, off Grand Manan, Bay of Fundy, Canada. J. Shellfish Res. 10: 286-292.

Li-Xun, Y., D.A. Ritz, G.E. Fenton and M.E. Lewis. 1991. Tracing the influence on sediments of organic waste from a salmonid farm using stable isotope analysis. J. Exp. Mar. Biol. Ecol. 145: 161-174.

McGhie, T.K., C.M. Crawford, I.M. Mitchell and D. O'Brien. 2000. The degradation of fish-cage waste in sediments during fallowing. Aquaculture 187: 351-366.

Milewski, I. 2000. Impact of salmon aquaculture on the coastal environment: a review. Discussion Document for Marine Aquaculture and the Environment, SeaWeb. 34 p.

Milewski, I., J. Harvey and B. Buerkly. 1997. After the gold rush: the status and future of salmon aquaculture in New Brunswick. Conservation Council of New Brunswick, Fredericton, NB. 61 p.

Milligan, T.G. and D.H. Loring. 1997. The effect of flocculation on the size distributions of bottom sediments in coastal inlets: implications for contaminant transport. Water, Air Soil Pollut. 99: 33-42.

Petrell, R.J., K. Mazhari Tabrizi, P.J. Harrison and L.D. Druehl. 1993. Mathematical model of Laminaria production near a British Columbia salmon sea cage farm. J. Appl. Phycol. 5: 1-14.

Pillay, T.V.R. 1992. Aquaculture and the environment. John Wiley & Sons, New York, NY. 185 p.

Pocklington, P., D.B. Scott and C.T. Schafer. 1994. Polychaete response to different aquaculture activities. Mém. Mus. Natl. Hist. Nat. Zool. 162: 511-520.

Pohle, G. and B. Frost. 1997. Establishment of standard benthic monitoring sites to assess long-term ecological modification and provide predictive sequence of benthic communities in the inner Bay of Fundy, New Brunswick. Atlantic Reference Centre, Huntsman Marine Science Centre, St. Andrews, NB. 119 p.

Pohle, G.W., S.S.L. Lim and B.R. Frost. 1994. Benthic monitoring of salmon aquaculture sites by the Huntsman Marine Science Centre: effects of organic enrichment on benthic macrofaunal communities in the lower Bay of Fundy, p. 92-100. In B.M. MacKinnon and M.D.B. Burt [eds.]. Proceedings of the Workshop on Ecological Monitoring and Research in the Coastal Environment of the Atlantic Maritime Ecozone. Environment Canada, Atlantic Region Occ. Rep. 4.

Rosenberg, R. 1985. Eutrophication- the future marine coastal nuisance. Mar. Pollut. Bull. 16: 227-231.

Rosenthal, H. 1988. Report of the ad hoc study group on environmental impact of mariculture. Int. Coun. Explor. Of the Sea, Copenhagen. ICES Coop. Res. Rep. 154. 83 p.

Rosenthal, H. [ed.]. 1994. Proceedings of a workshop on fish farm effluents in EC countries. J. Appl. Ichthyol. 10: 10-45.

Rosenthal, H., D. Scarratt and B. McInerney-Northcott. 1995. Aquaculture and the environment, p. 451-500. In A.D. Boghen [ed.]. Cold water aquaculture in Atlantic Canada. 2nd edition. Can. Inst. Res. Reg. Dev. Moncton, NB.

Samuelsen, O.B., V. Torsvik and A. Ervik. 1992. Long-range changes in oxytetracycline concentration and bacterial resistance towards oxytetracycline in a fish farm sediment after medication. Sci. Total Environ. 114: 25-36.

Silvert, W. 1994e. Modelling benthic deposition and impacts of organic matter loading, p.1-18. In B.T. Hargrave [ed.]. Modelling benthic impacts of organic enrichment from marine aquaculture. Can. Tech. Rep. Fish. Aquat. Sci. 1949: xi + 125 p.

Silvert, W. and B.T. Hargrave. 1995. Report on International Workshop on Environmental Interactions of Mariculture. Proc. ICES Annual Science Conference, C.M. 1995/F:6 (Sess. F).

Soulsby, P.G., D. Lowthion and M. Huston. 1982. Effects of macroalgal mats on the ecology of intertidal mudflats. Mar. Pollut. Bull. 13: 162-166.

Stewart, J.E. 1994. Aquaculture in Atlantic Canada and the research requirements related to environmental interactions with finfish culture, p. 1-18. In A. Ervik, P. Kupka Hansen and V. Wennevik [eds.]. Proceedings of the Canada-Norway Workshop on Environmental Impacts of Aquaculture. Fisken Havet 13.

Stewart, J.E. 2001. A case for a comprehensive environmental data base as a tool for integrated coastal zone planning and management. Bull. Aquacult. Assoc. Canada 101-1: 42-47.

Stewart, J.E., E.C. Penning-Rowsell and S. Thornton. 1993. The LENKA Project and coastal zone management in Norway, p. 259-281. In OECD documents: Coastal zone management selected case studies. OECD, Paris, France.

Strain, P.M. and P.A. Yeats. 1999. The relationships between chemical measures and potential predictors of the eutrophication status of inlets. Mar. Pollut. Bull. 38: 1163-1170.

Strain, P.M., D.J. Wildish and P.A. Yeats. 1995. The application of simple models of nutrient loading and oxygen demand to the management of a marine tidal inlet. Mar. Pollut. Bull. 30: 253-261.

Sutherland, T.F., A.J. Martin and C.D. Levings. 2001. The characterization of suspended particulate matter surrounding a salmonid net-pen in the Broughton Archipelago, British Columbia. ICES J. Mar. Sci. 58: 404-410.

Sutherland, T.F., C.D.Levings, J.M. Helfield, B.T. Hargrave, W. Knapp and D. Stucchi. 2002. Research tools in support of Habitat Management priorities, p. 5-8. In B.T. Hargrave [ed.]. Environmental Studies for Sustainable Aquaculture (ESSA): 2002 workshop report. Can. Tech. Rep. Fish. Aquat. Sci. 2411: v + 117 p.

Valiela, I., G. Collins, J. Kremer, K. Lajtha, M. Geist, B. Seely, J. Brawley and C.H. Sham. 1997. Nitrogen loading from coastal watershed to receiving estuaries: new methods and application. Ecol. Appl. 7: 358-380.

Warwick, R.M. 1986. A new method for detecting pollution effects on marine macrobenthic communities. Mar. Biol. 92: 557-562.

Warwick, R.M. 1987. Detection of pollution effects on marine macrobenthos: further evaluation of the species abundance/biomass method. Mar. Biol. 95: 193-200.

Weston, D. 1990. Quantitative examination of macrobenthic community changes along an organic enrichment gradient. Mar. Ecol. Prog. Ser. 61: 233-244.

Wong, M., M.A. Barbeau and R.A. Aiken. 1999. Intertidal invertebrate population density and diversity: does salmon aquaculture play a role, p. 89-100. In J. Ollerhead, P.W. Hicklin, P.G. Wells and K. Ramsey [eds.]. Understanding change in the Bay of Fundy ecosystem. Proc. 3rd Bay of Fundy Workshop. Environment Canada, Occ. Rep. 12.

Ye, L.-X., D. Ritz, G.E. Fenton and M.E. Lewis. 1991. Tracing the influence on sediments of organic waste from a salmon farm using stable isotope analysis. J. Exp. Biol. Ecol. 145: 161-174.

Yeats, P.A. 2002. Trace metal tracers of fish farm wastes. 2002, p. 80-83. In B.T. Hargrave [ed.]. Environmental Studies for Sustainable Aquaculture (ESSA): 2002 workshop report. Can. Tech. Rep. Fish. Aquat. Sci. 2411: v + 117 p.

   

   

Last updated : 2005-04-06

Important Notices