One of the most significant ecological and economic impacts of exotic species is associated with their role as vectors for the introduction of parasites into invaded areas. Exotic parasites may have devastating impacts on invaded ecosystems; moreover, invaders may also become hosts for aboriginal parasites, promoting native diseases that otherwise would not have emerged. During 2009 and 2010, exotic molluscs were collected from 27 sites in the Lower Great Lakes and their tributaries, the Finger Lakes, and Lake Oneida. Seven species of exotic molluscs were examined for the presence of trematodes, including the zebra mussel (Dreissena polymorpha), quagga mussel (Dreissena rostriformis bugensis), faucet snail (Bithynla tentaculata), European stream valvata (Valvata piscinalis), Asian clam (Corbicula fluminea), Chinese mystery snail (Cipangopaludina chinensis), and the New Zealand mudsnail (Potamopyrgus antipodarum). Most of the examined molluscs were infected with trematode larvae that may be harmful to their subsequent vertebrate hosts, including fish, birds, and mammals. These included Sphaeridiotrema sp. cercariae and Cyathocotyle bushiensis metacercariae from B. tentaculata, Echinostoma sp. cercariae from V. piscinalis, and echinostomatid metacercariae from Dreissena spp. and C. fluminea. Many exotic molluscs that were believed to be free of parasites have already acquired trematodes native to North America. Hotspots of trematode infections were recorded in the western basin of Lake Erie and in Lake Oneida, where several species of exotic molluscs had a high prevalence of trematodes, and thus potentially pose risk of transmission to definitive hosts.
Journal of Shellfish Research (2012) 31(3): 885-894

The zebra mussel (Dreissena polymorpha) and its congener the quagga mussel (Dreissena rostriformis bugensis) are both invaders in freshwater, but have very different invasion histories, with zebra mussels attaining substantially faster rates of spread at virtually all spatial scales. However, in waterbodies where they co-occur, D. r. bugensis can displace D. polymorpha. To determine if the mechanisms for this displacement are associated with different survival and growth, we kept mussels in flow-through tanks for 289 days with two temperature regimes that mimicked the natural surface water (littoral zone) and hypolimnion conditions of Lake Erie. For the littoral zone regime, we used water directly from the surface of Lake Erie (range 4–25°C, average 11.9 ± 0.6°C). For the profundal zone treatment, Lake Erie surface water was chilled to about 6°C (range 5–8°C, average 6.2 ± 0.6°C) for the full duration of the experiment. For each of these temperature regimes, we used three replicate tanks with only zebra mussels present and three replicate tanks with only quagga mussels (150 ind./tank each), and three replicate tanks with both species (75 ind./tank of each species). Quagga mussels had higher survivorship and grew more than zebra mussels in all treatments. For both species, the size of the mussel entering the winter was critical for survivorship. Larger mussels had a higher survival over the winter in all treatments. For both species, there was a survivorship and growth tradeoff. In the warmer littoral zone treatment both species had higher growth, but lower survival than in the colder profundal zone treatment. Surprisingly, although quagga mussels outperformed zebra mussels, zebra mussel survivorship was better when they were faced with competition by quagga mussels than with just intraspecific competition. In addition, quagga mussels suffered size-specific mortality during the growing season only when facing interspecific competition with zebra mussels. Further experiments are needed to determine the possible mechanisms for these interspecific effects.
Hydrobiologia (2010) 668(1): 183-194

Aim: Exotic species may serve as vectors for the introduction of parasites from their native range and may also become infected by parasites already present in invaded areas, but the total number of parasites infecting such exotic species in their invaded areas is typically less than that in their native range. We tested whether the diversity of parasites associated with exotic species in the native and invaded areas is related to the epizootic impact these parasites cause. Location: Global. Methods: We examined the diversity and epizootic impact of 384 parasite taxa associated with 22 exotic freshwater invertebrate species. The epizootic impact of each parasite was rated based on whether it had been documented to cause a major pathological impact on a large proportion of an infected host population (other than the invader under consideration). Results: The total number of parasites associated with an exotic host in its native range was about twice that of all parasites associated with it in its entire invaded range. This was mainly because of the loss in the invaded areas of low impact parasites, whereas the average number of high impact parasites per host in these areas did not differ statistically from that in the native range. Main conclusions: Our study suggests similar levels of adverse impact of parasites of exotic species in both their native and invaded areas. In addition to the introduction of highly pathogenic exotic parasites, other mechanisms that may be involved include (1) acquisition by the invaders of new high impact parasites in the invaded ranges, (2) high abundance of the invaders in their new ranges and (3) susceptibility of novel hosts to exotic parasites because of the ‘naive host syndrome’.
Diversity and Distributions (2010) 16: 798–803

The assessment of risks associated with alien invasive organisms implies a detailed knowledge of their taxonomical composition and distribution within an assessment unit. In this paper we used both literature data and results from our field surveys of more than forty sites, conducted in 2006-2008, to compile a checklist of aquatic alien species (invertebrates and fish) established in the three large river basins of Belarus (Dnieper, Pripyat, Neman). Thirty six alien species have been revealed, most of which are of Ponto-Caspian origin. The discovery of several new species during our surveys indicates that the rate of introductions has substantially increased over the last two decades.
Aquatic Invasions (2009) Volume 4, Issue 2: 337-347