Ontogenetic Change in Behavioral Responses to Structural Enrichment From Fry to Parr in Juvenile Atlantic Salmon ( L.).

Enrichment is widely used as a tool for studying how changes in environment affect animal behavior. Here, we report an experimental study investigating if behaviors shaped by stimuli from environmental enrichment depending on the stage animals are exposed to enrichment. We used juvenile Atlantic salmon () in their first autumn.

Life history shifts in an exploited African fish following invasion by a castrating parasite.

Evolutionary theory predicts that infection by a parasite that reduces future host survival or fecundity should select for increased investment in current reproduction. In this study, we use the cestode and its intermediate fish host in Wissman Bay, Lake Nyasa (Tanzania), as a model system. Using data about infection of fish hosts by collected for a period of 10 years, we explored whether parasite infection affects the fecundity of the fish host , and whether host reproductive investment has increased at the expense of somatic growth.

The tapeworm Ligula intestinalis alters the behavior of the fish intermediate host Engraulicypris sardella, but only after it has become infective to the final host.

Ligula intestinalis is a tapeworm using copepods and cyprinid fish as intermediate hosts and fish-eating birds as final hosts. Since some parasites can increase their own fitness by manipulating the behavior of the intermediate host, we explored if this parasite affected predator avoidance, swimming activity and depth preference of the fish intermediate host, Engraulicypris sardella. We found that when L.

Invest more and die faster: The life history of a parasite on intensive farms.

Organisms are expected to respond to alterations in their survival by evolutionary changes in their life history traits. As agriculture and aquaculture have become increasingly intensive in the past decades, there has been growing interest in their evolutionary effects on the life histories of agri- and aquacultural pests, parasites, and pathogens. In this study, we used salmon lice () to explore how modern farming might have affected life history evolution in parasites.

Spatial and temporal distribution of Ligula intestinalis (Cestoda: Diphyllobothriidea) in usipa (Engraulicypris sardella) (Pisces: Cyprinidae) in Lake Nyasa.

Engraulicypris sardella is an endemic and economically important cyprinid species in Lake Nyasa/Malawi which has recently been infected by the tapeworm Ligula intestinalis. This parasite is known to induce severe pathological and behavioural effects on other cyprinids, including castration, followed by a collapse of infected populations. As a first step to understanding the dynamics between this parasite and E.

Evolution of virulence under intensive farming: salmon lice increase skin lesions and reduce host growth in salmon farms.

Parasites rely on resources from a host and are selected to achieve an optimal combination of transmission and virulence. Human-induced changes in parasite ecology, such as intensive farming of hosts, might not only favour increased parasite abundances, but also alter the selection acting on parasites and lead to life-history evolution. The trade-off between transmission and virulence could be affected by intensive farming practices such as high host density and the use of antiparasitic drugs, which might lead to increased virulence in some host-parasite systems.

The role of chewing lice (Phthiraptera: Philopteridae) as intermediate hosts in the transmission of Hymenolepis microps (Cestoda: Cyclophyllidea) from the willow ptarmigan Lagopus lagopus (Aves: Tetraonidae).

The cestode Hymenolepis microps is an intestinal parasite of tetraonid birds, including the willow ptarmigan (Lagopus lagopus). This parasite is able to maintain a high prevalence and intensity throughout the year, even in a subarctic environment in bird populations with relatively low host densities, indicating effective transmission routes. Willow ptarmigan consume mainly vegetal material and active consumption of invertebrates is confined to the first two or three weeks of life.

Parasite fecundity decreases with increasing parasite load in the salmon louse Lepeophtheirus salmonis infecting Atlantic salmon Salmo salar.

Aggregation is common amongst parasites, where a small number of hosts carry a large proportion of parasites. This could result in density-dependent effects on parasite fitness. In a laboratory study, we explored whether parasite load affected parasite fecundity and survival, using ectoparasitic salmon lice (Lepeophtheirus salmonis Krøyer, 1837) infecting Atlantic salmon (Salmo salar) hosts.

Atlantic salmon infected with salmon lice are more susceptible to new lice infections.

Aggregation is commonly observed for macroparasites, but its adaptive value remains unclear. Heavy infestations intensities may lead to a decrease in some fitness-related traits of parasites (e.g.

When to Reproduce? A New Answer to an Old Question.

We present a life-history model based on the assumptions that juvenile survival follows a negative exponential function and that fecundity gain increases linearly with time to maturity. This model predicts that the optimal fitness is achieved when survival at maturity is 0.368 (e(-1)).

Life history and virulence are linked in the ectoparasitic salmon louse Lepeophtheirus salmonis.

Models of virulence evolution for horizontally transmitted parasites often assume that transmission rate (the probability that an infected host infects a susceptible host) and virulence (the increase in host mortality due to infection) are positively correlated, because higher rates of production of propagules may cause more damages to the host. However, empirical support for this assumption is scant and limited to microparasites. To fill this gap, we explored the relationships between parasite life history and virulence in the salmon louse, Lepeophtheirus salmonis, a horizontally transmitted copepod ectoparasite on Atlantic salmon Salmo salar.

Intensive Farming: Evolutionary Implications for Parasites and Pathogens.

An increasing number of scientists have recently raised concerns about the threat posed by human intervention on the evolution of parasites and disease agents. New parasites (including pathogens) keep emerging and parasites which previously were considered to be 'under control' are re-emerging, sometimes in highly virulent forms. This re-emergence may be parasite evolution, driven by human activity, including ecological changes related to modern agricultural practices.

Parasite abundance, body size, life histories, and the energetic equivalence rule.

If common processes generate size-abundance relationships among all animals, then similar patterns should be observed across groups with different ecologies, such as parasites and free-living animals. We studied relationships among body size, life-history traits, and population intensity (density in infected hosts) among nematodes parasitizing mammals. Parasite size and intensity were negatively correlated independently of all other parasite and host factors considered and regardless of type of analyses (i.

On the track of the Red Queen: bark beetles, their nematodes, local climate and geographic parthenogenesis.

Geographic parthenogenesis has been explained as resulting from parasite pressure (Red Queen hypothesis): several studies have found high degrees of sexuals where the prevalence of parasites is high. However, it is important to address whether prevalence of parasites mirrors risk of infection. We explored geographic parthenogenesis of Ips acuminatus bark beetles and their nematodes.

Empirical support for optimal virulence in a castrating parasite.

The trade-off hypothesis for the evolution of virulence predicts that parasite transmission stage production and host exploitation are balanced such that lifetime transmission success (LTS) is maximised. However, the experimental evidence for this prediction is weak, mainly because LTS, which indicates parasite fitness, has been difficult to measure. For castrating parasites, this simple model has been modified to take into account that parasites convert host reproductive resources into transmission stages.

Disease dynamics: all caused by males?

Some host individuals tend to acquire parasites at a much faster rate than do others--a consequence of heterogeneities in susceptibility and/or exposure. This is termed 'overdispersion' and, as for many other statistical phenomena, the degree of overdispersion often conforms to a 20/80 rule, where 20% of the host population is responsible for approximately 80% of the parasite transmission. But which are the hosts driving so much of the dynamics of an infectious disease? If host individuals at the tail of the frequency distribution can be identified by some common label, controlling parasitic diseases would be much easier.

Vector-borne parasites decrease host mobility: a field test of freeze or flee behaviour of willow ptarmigan.

Transmission mode has been suggested to be a strong predictor of virulence. According to theory, the transmission of vector-borne parasites should be less dependent on host mobility than directly transmitted parasites. This could select for increased exploitation of host resources in parasites transmitted by vectors, which may be manifested as higher virulence.

Standard sampling techniques underestimate prevalence of avian hematozoa in willow ptarmigan (Lagopus lagopus).

A total of 68 willow ptarmigan (Lagopus lagopus L.) was collected during September 1995 from two localities in Troms County, northern Norway. Thin blood smears were prepared and examined for blood parasites.

The parasite Lernaeocera branchialis on caged cod: infection pattern is caused by differences in host susceptibility.

Variation in host susceptibility causes significant differences in infection rates between hosts living in a semi-natural situation. Such knowledge has implications for population dynamics and evolutionary models of host-parasite interactions as well as for estimations of parasite abundance. Infection rates by Lernaeocera branchialis (L.

Experimental Elaphostrongylus alces infection in goats.

Five goats aged 4 months were each inoculated with approximately 300 third-stage larvae of Elaphostrongylus alces, and killed for post-mortem examination after 14-150 days. No clinical signs of disease were observed during the experiment. Pathological examination revealed that the larvae penetrated the walls of the abomasum and small intestine and migrated towards the caudal vertebral canal.

Aspects of the life cycle and pathogenesis of Elaphostrongylus cervi in red deer (Cervus elaphus).

Aspects of the migratory life cycle and pathogenesis of Elaphostrongylus cervi were studied in red deer (Cervus elaphus) using 2 farmed calves experimentally infected with 450 third-stage larvae killed 40 and 45 days postinfection and using 3 wild calves and 3 wild yearlings with natural infections killed during autumn hunting. A full necropsy was carried out on the experimental calves, but only the head, eviscerated carcass, and lungs were examined from the naturally infected animals. Histological examination included extensive studies of the central nervous system (CNS), spinal nerve roots, and lungs.

Experimental Elaphostrongylus cervi infection in sheep and goats.

The pathogenesis and migratory life cycle of Elaphostrongylus cervi were studied in four sheep and six goats killed and examined 6 days to 5 months after inoculation with infective third-stage larvae (L3). Detailed histological studies demonstrated that the L3 followed a porto-hepatic, and probably also a secondary lymphatic, migratory route from the abomasum and small intestine to the lungs, with subsequent spread via the general circulation to the central nervous system (CNS) and other tissues. In addition, the results suggested that haematogenously spread L3, arrested in arterial vessels outside the spinal cord, migrated into the cord along the spinal nerves.

Cross-infection of moose (Alces alces) and reindeer (Rangifer tarandus) with Elaphostrongylus alces and Elaphostrongylus rangiferi (Nematoda, Protostrongylidae): effects on parasite morphology and prepatent period.

Moose (Alces alces) and reindeer (Rangifer tarandus) were experimentally cross-infected with Elaphostrongylus rangiferi and Elaphostrongylus alces, respectively. Both Elaphostrongylus species completed their development in the alternate hosts but produced fewer larvae than in their usual host species. Reindeer infected with Elaphostrongylus alces developed patent infections after 39-130 days.

The evolution of tissue migration by parasitic nematode larvae.

Migration by nematode larvae through the tissues of their mammalian hosts can cause considerable pathology, and yet the evolutionary factors responsible for this migratory behaviour are poorly understood. The behaviour is particularly paradoxical in genera such as Ascaris and Strongylus in which larvae undergo extensive migrations which begin and end in the same location. The orthodox explanation for this apparently pointless behaviour is that a tissue phase is a developmental requirement following the evolutionary loss of skin penetration or intermediate hosts.