Lepeophtheirus salmonis (Copepoda: Caligidae)

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Contributions to Zoology. 69 (1/2) 71-77 (2000) SPB Academic Publishing bv, The Hague Lepeophtheirus salmonis (Copepoda: Caligidae) on farmed salmon in Ireland David Jackson, Daniel Hassetț Sandra Deady & Yvonne Leahy Marine Institute, Ross House, Merchants Road, Galway, Ireland Keywords: sea lice, farmed salmon, Lepeophtheirus salmonis Abstract Costello (1991). The results of monitoring in 1991 The investigation of specific characteristics of Lepeophtheirus and 1992 showed that lice burdens on two seawinter fish were significantly higher than on one salmonis populations on farmed salmon was made possible by the examinationofthe parasite infestationparameters ofregular non destructive samples taken for to six in five up years bays. Perennial persistence of seasonal patterns of infestation as exhibited by intensity, prevalence and abundance was examined. Site specific characteristics were detected which appeared to be independent of inter-annual variations. Seasonal variations in individual lice size and fecundity, and temporal variation in population dynamics on the farmed fish in the five bays are considered in the context ofthe not inconsiderable changes in husbandry and lice control practices which have been introduced in the industry over the six year period. sea-winter fish (Jackson and Minchin, 1993). The lice on two sea-winter fish were considered to be a reservoir of infection for one sea-winter fish and smolts on multi-generation sites. On the basis of these results, a new initiative in salmon farm management put in place by the Department of was Marine. This involved the separation of generations, annual fallowing and the early harvest of two sea-winter fish to reduce vertical and lateral transmission of lice infestations. A parallel initiative to optimise treatment was regimes undertaken Contents Introduction 71 Materials and methods 71 Results 73 Infestation parameters 73 Infestation to host sea-age 73 Somatic size and egg string length 74 Discussion 74 References 76 jointly by the industry and the regulatory authorities. These changes in husbandry practices had a profound impact on the pattern of lice infestations on farmed salmon in Ireland (Jackson et al. 1997). Despite the major changes which have occurred in lice management and control over this period, certain characteristics of Lepeophtheirus salmonis (Kroyer) populations on farmed salmonids have These persisted. are presented here by reference to records from five bays sampled as part of the national sea lice monitoring programme in Ireland. Introduction Monitoring of the levels of sea lice infestation on Materials and methods salmonid farms in Ireland commenced in 1991. When monitoring commenced in 1991 the main The sampling methodology, the regime of annual heatinent employed in the control of sea lice was sampling of salmonid farms in Ireland and the Nuvan 500 EC, a 50% solution of Dichlorvos. This protocol for the handling and analysis of samples ls a bath treatment and the limitations to its efficacy and usefulness are described in Jackson and is set out in Jackson et al. (1997). Generally two cages of fish were sampled for each population of

Lepeophtheirus 72 D. Jackson et al. - salmonis on farmed salmon in Ireland Fig. I. Prevalence, mean intensity and mean abundance of Lepeophtheirus salmonis on I sea-winter salmon (Salmo salar) in (a) Lough Swilly and (b) Kilkieran Bay. prevalence; mean intensity; mean abundance. fish on site; a standard cage,which was sampled at arithmetic means obtained according each inspection, and another selected at ran- cage to the following protocol: A sample of approximately thirty dom at each inspection. Different year classes of fish was taken from a single cage. The fish were fish were considered as different populations, as anaesthetised and all mobile lice were removed and were different species (i.e. Salmon salar, Oncor- preserved in alcohol. All lice remaining in the hynchus mykiss). anaesthetic after the sample was processed were The two tailed t-test, corrected for multiple testing retained and included in the sample. All lice were (Bonferoni method), was used for testing signifi- identified and staged. For each sample a mean cance of somatic size and egg string length was analysed using Spearman s rank correlation. Lice counts presented in this paper are based on number of lice in each category was obtained by dividing the number of lice recorded by the number of fish examined.

Contributions to Zoology, 69 (1/2) - 20000 73 Fig- 2. Mean abundance of Lepeophtheirus salmonis.on salmon of separate generations from Kenmare Bay, Clew Bay and Lough Swilly. Year numbers refer to the generation = of salmon examined. Month I January etc. Results descriptor of lice infestation. Even where percentage prevalence was less that 100%, intensity data closely Infestation parameters mirrored trends in abundance values (Fig. 1). Data were examined from farms in five bays along hie west coast; Lough Swilly, Clew Bay, Kilkieran D a y, Kenmare Bay and Bantry Examination Bay. oi Prevalence, intensity and abundance data for 1e five bays showed that abundance was a good Infestation relative to host sea-age Lice infestation for six generations of farmed salmon is shown in terms of mean abundance in Figure 2.

Lepeophtheirus 74 D. Jackson et al. - salmonis onfarmed salmon in Ireland Fig. 2 (continued). Mean suggests the presence of a low and probably vary- abundance of Lepeophtheirussalmonis on salmon of separate generations from Kilkieran Bay and Bantry Bay. Year numbers refer to the = generation ofsalmon examined. Month 1 January etc. At the five sites examined, the progression of infestation over time for a given generation of fish in Lough Swilly (two tailed t-test, corrected for multiple testing; P< 0.05). The mean egg string was extraordinarily stable for individual sites. The progression in infestation can be described by the slope of the log lice abundance plotted against date. length was more variable, but in general, egg string length co-varied with somatic size (Spearman s rank correlation; P<0.05). While there was considerable inter-annual variation, (here were also underlying trends as exemplified by three consecutive growing seasons Kilkieran Bay (Fig. 3). in Discussion Recruitment of L. salmonis on the high seas has been reported from both the Pacific Ocean Somatic size and egg string length (Nagasawa, 1987) and the Atlantic Ocean (Jacobsen and Gaard, 1997). Jacobsen and Gaard (op. cit.) The somatic size of ovigerous female L. salmonis recorded the presence of both pre-adult and chalimus and egg string length, as an index of fecundity, were examined at five sites (Table I). Somatic size stages of L. salmonis on wild and escaped Atlantic salmon caught on long lines north of the Faroe rose from December through spring to an il Islands. They also found an increase in the abun- maximum. Somatic size then progressively decreased through the summer into autumn. This dance of lice with sea-age of the host. This conclusive evidence of high seas transmission of lice change in mean somatic length was significant in all cases except between December and February infestation far from spawning aggregations of hosts,

- 20000 Contributions to Zoology, 69 (1/2) 75 f'lg 3. Monthly log mean abundance for Lepeophtheirus salmonis for three consecutive years in Kilkieran Bay

76 D. Jackson et al. - Lepeophtheirus salmonis on farmed salmon in Ireland Table I. Somatic size and egg string length for Lepeophtheirus salmonis. SITE DATE N Mean S.E. Median Mean S.E. Median Lough Swilly Dec 96 31 10.58 0.18 10.80 11.79 0.64 11.20 Feb 97 28 10.76 0.38 11.10 14.33 0.64 14.70 97 31 12.23 0.17 12.10 15.18 0.37 15.40 Clew Bay Feb 96 14 11.44 0.22 11.40 13.60 1.06 13.10 96 3 10.81 0.31 10.70 15.67 2.70 16.50 Jul 96 23 10.72 0.15 10.75 14.43 0.76 15,62 Killary Hbr Jan 96 20 12.50 0.28 12.60 23.10 1.34 24.70 96 30 12.81 0.12 12.55 25.05 1.01 26,50 Mannin Bay Jan 96 30 11.16 0.24 11.50 20.81 0.85 20,35 96 30 12,69 0.17 12.70 18.48 1.06 18.40 Kilkieran Bay Dec 96 30 11.05 0.15 10.86 17.24 0.48 17.03 97 28 11.50 0,16 11.40 12.39 0.79 11.24 Jul 97 30 11.26 0,13 11.37 18.18 0.56 18.57 Aug 97 30 10.06 0.11 09.95 12.55 0.41 13.24 Oct 97 30 9.84 0.12 09.81 13.18 0,37 13.16 ing level of infective stages of L. salmonis in the consistent with regular reports from fish farmers open sea over long of time. periods This is compatible with the long term trends observed at the of increased infestation pressure, often in the absence of increased numbers of ovigerous females, five relatively oceanic fish farm sites examined in in the spring. A spring maximum in reproductive this study and the findings of Boxaspen (1997). In the presence of ongoing sources of infestation from output may have adaptive significance for a parasite whose hosts migrate to sea in large numbers at this precise time of the year. within and outside the farm, lice infestation parameters will tend to increase with of the sea-age host in spite of effective lice control measures. Costelloe ct al. (1995) concluded that there was a References potential for relatively high concentrations of lice larvae, originating from wild salmonids, to be Boxaspen K. 1997. Geographical and temporal variation in present at specific times of the year. The fact that infective copepodids concentrate layers during the day, as do feeding (Heuch et al. in the surface farmed salmon, 1995) means that such concentrations are likely to have maximum on impact farmed abundance of salmon lice ( Lepeophtheirus salmonis) on salmon (Salmo salar L.). ICES J. Mar. Sci. 54: 1144-1147. Costelloe J, Costelloe M, Roche N. 1995. Variation in sea lice infestation on Atlantic salmon smolts in Killary Harbour, West Coast of Ireland. Aquaculture International. fish. Such pulses of infestation are capable of be- 3: 379-393. Heuch PA, Parsons A, Boxaspen K. 1995. Did Vertical Migration - a possible host finding mechanism in salmon louse (Lepeophtheirus salmonis) copepodids. Can. J. Fish. Aquat. Sci. 52: 681-689. Jackson D, Costello M. 1991. Dichlorvos and alternative ing neutralised by targeted treatments in a way that a constant level of infestation, even at a relatively low level, cannot. The varying level of background sources of infestation may be a key parameter in determining the practical minimum levels of infestation which can be attained by lice management strategies as outlined in Jackson et al. (1997). The spring maxima in somatic size and associ- sealice treatments. In: Pauw N de, Joyce J, eds. Aquaculture and the Environment. Gent: European Aquaculture Society, 215-221. Jackson D, Minchin 1). 1992. Aspects of the reproductive output of two caligid copepod species parasitic on cultivated salmon. Inv. Reprod. Dev. 22: 87-90. ated egg string length reported in this study are Jackson D, Minchin D. 1993. Lice infestations of farmed

20000 Contributions to Zoology, 69 (1/2) - 77 salmon in Ireland. In; Boxshall GA, Defaye D, eds. Patho- and escaped farmed Atlantic salmon (Salmo salar L.), gens of wild and farmed fish. London; Ellis Horwood, ICES J. Mar. Sci. 54: 1113-1119. 188-201. Jackson D, Deady S, Leahy Y, Hassell D. 1997. Variations in parasitic caligid infestations on farmed salmonids Nagasawa K. 1987. Prevalence and abundance of Lepeophtheirus salmonis (Copepoda : Caligidae) on high seas salmon and trout in the North Pacific Ocean. Nippon Suisan and implications for their ICES J. Mar. Sci. management. Gakkaishi. 53(12): 2151-2156. 54: 1104-1112. Jacobsen JA, Gaard E. 1997. Open-ocean infestation by salmon lice (Lepeophtheirus salmonis)): comparison ofwild Received: 18 March 1999