Pheromone-induced spawning of Pacific herring. I. Behavioral characterization.

A spawning pheromone in the milt (semen) and testes of the Pacific herring, Clupea harengus pallasi, triggers spawning in sexually mature fish of both sexes and is thought to facilitate school spawning of this species. We found the response to the pheromone to be a stereotyped behavioral sequence consisting of a graded extension of the gonadal papilla, release of gametes, and spawn deposition behavior. The response is triggered by an olfactory stimulus, as demonstrated by the elimination of the response by occlusion of the nares. Stimulus concentrations of an approximate 1:500 dilution of fresh milt or the equivalent of 0.02 g of fully mature testes per milliliter were required to elicit a response in 50% of ripe herring that are responsive to the pheromone. Female fish appeared to be less sensitive to the pheromone in milt than males early in the spawning season, but not thereafter. The average duration of responses of male fish was longer after exposure to concentrated milt than to testes extracts, but no consistent difference in response times of the two sexes was detected. Factors other than the spawning pheromone, maturity of the fish, and stress also were found to influence the spawning response. For example, exposure to shallow (3 cm) water in a small tank induced "spontaneous" papilla extension and spawning approximately 20 min after refilling the tank; occluding the nares prevented this response. Also, the presence of floating kelp (Macrocystis) resulted in prolonged spawning in a large tank after pheromonal stimulation.

The effect of vaccination and sea water entry on immunocompetence and susceptibility to Kudoa thyrsites in Atlantic salmon (Salmo salar L.).

The effect of intraperitoneal (IP) vaccination and sea water entry (SWE) on the immunocompetence of Cascade Atlantic salmon was investigated. Smolts were IP injected with Aqua Health's Forte trade mark vaccine (Listonella (Vibrio) anguillarum, Listonella ordalii, Vibrio salmonicida and Aeromonas salmonicida) at four times (42, 238, 433 and 630 degree days, DD) prior to SWE and were examined for immunocompetence. Immune response measurements included mitogen-driven proliferation of peripheral blood leukocytes (PBL), head kidney leukocyte respiratory burst activity and alternative complement hemolytic titres and were measured 24h prior to SWE, 72 h post-SWE and again 3.5 weeks post-SWE. A 50% reduction in the number of PBL was observed 3 days post-vaccination. At this time LPS-driven proliferation was low (stimulation index, SI, 1.5-2.9) in all groups prior to SWE compared with that of PBL from freshwater-reared Atlantic salmon parr (6.7). By 72 h and 3.5 weeks post-SWE, the LPS-driven SI from unvaccinated salmon and those vaccinated 630 and 433 DD prior to SWE increased 3-fold. In contrast, SI from salmon vaccinated 42 and 238 DD prior to SWE remained low. A similar pattern was observed for cultured PBL stimulated with PHA, although unlike LPS-stimulated PBL, the SI of cells from parr and unvaccinated control smolts remained low following SWE but increased in fish vaccinated 433 and 630 DD prior to SWE. The respiratory burst activity of head kidney leukocytes was not affected by SWE but showed a transient 50% depression 3 days post-vaccination. The alternative complement activity (ACH50) was similar for all treatment groups prior to and at 72h post-SWE. By 3.5 weeks post-SWE, ACH50 values in salmon vaccinated 42 and 238 DD prior to SWE doubled to 874 and 860 U/ml, respectively. The prevalence and severity of Kudoa thyrsites infections, detected in all treatment groups approximately 2400 DD following SWE, were not significantly different among groups. Atlantic salmon parr should be IP vaccinated no earlier than 433 DD before SWE to avoid an enhanced risk of acquiring pathogens because of transient depression in some immune mechanisms.