Levels of intra-host and temporal sequence variation in a large <Emphasis Type="Italic">CO</Emphasis>1 sub-units from <Emphasis Type="Italic">Anisakis simplex sensu stricto</Emphasis> (Rudolphi 1809) (Nematoda: Anisakisdae): implications for fisheries management

This paper is the first to address the suitability and potential of the cytochrome oxidase-1 (CO1) region of the parasitic marine nematode Anisakis simplex sensu stricto as a genetic marker. A. simplex s.s. is an ubiquitous parasite of many marine organisms and has been used as a ‘biological tag’ for population studies of pelagic fish stocks. The CO1 marker informs not only about nematode population structure but also about its hosts. The large CO1 sub-unit (∼800 bp) was analysed from third stage larvae of A. simplex s.s. from Atlantic herring, Clupea harengus L. caught off the north-west coast of Scotland. In total 161 A. simplex s.s. CO1 sequences were analysed from 37 herring that represented three spawning periods over 2 years. Overall very high haplotype and low nucleotide diversities were observed (h = 0.997 and π = 0.008, respectively). These results are in keeping with studies investigating parasitic nematodes of ungulates and are symptomatic of the high rate of substitutions accumulated by mtDNA and effective dispersal strategies of the parasite. The Tamura-Nei I + Г (Г = 1.2243) model of nucleotide substitution best suited the present data which were dominated by a high thymine bias and associated transitions. Large within population differences were highlighted by hierarchal AMOVAs with little variation related to spawning events or years which may indicate localised temporal stability. Temporal homogeneity in the CO1 gene coupled with the ubiquitous and widespread nature of the parasite indicates both the potential and limitations for its incorporation in stock-separation studies of its hosts. This work was carried out at the School of Biological Sciences, Liverpool University, Crown Street, Liverpool. L69 7ZB, UK.     

Inhibition of erythrocyte delta-aminolevulinic acid dehydratase (ALAD) activity in fish from waters affected by lead smelters

We assessed the effects on fish of lead (Pb) released to streamsby smelters located in Trail, BC (Canada), E. Helena, MT, Herculaneum, MO, and Glover, MO. Fish were collected by electrofishing from sites located downstream of smelters and from reference sites. Blood from each fish was analyzed for -aminolevulinic acid dehydratase (ALAD) activity and hemoglobin (Hb), and samples of blood, liver, or carcass were analyzed for Pb, zinc (Zn), or both. Fish collected downstreamof all four smelters sites had elevated Pb concentrations, decreased ALAD activity, or both relative to their respectivereference sites. At E. Helena, fish from the downstream site also had lower Hb concentrations than fish from upstream. Differences among taxa were also apparent. Consistent with previous studies, ALAD activity in catostomids (Pisces: Catostomidae-northern hog sucker, Hypentelium nigricans;river carpsucker, Carpiodes carpio; largescale sucker, Catostomus macrocheilus; and mountain sucker, C. platyrhynchus) seemed more sensitive to Pb-induced ALAD inhibition than the salmonids (Pisces: Salmonidae-rainbow trout,Oncorhynchus mykiss; brook trout, Salvelinus fontinalis) or common carp (Cyprinus carpio). Some of these differences may have resulted from differential accumulation of Zn, which was not measured at all sites. We detected no ALAD activity in channel catfish (Ictaluruspunctatus) from either site on the Mississippi River at Herculaneum, MO. Our findings confirmed that Pb is releasedto aquatic ecosystems by smelters and accumulated by fish, andwe documented potentially adverse effects of Pb in fish. We recommend that Zn be measured along with Pb when ALAD activityis used as a biomarker and the collection of at least 10 fish ofa species at each site to facilitate statistical analysis.