We compared the impact of exposure to seawater on three sockeye salmon (Oncorhynchus nerka) stocks: one that normally migrates to sea as underyearlings (sea-type) and two with the more common life history strategies of 1 (river-type) or 2 (lake-type) yr of freshwater residence prior to seaward migration. Innate differences in survival, ability to regulate tissue chlorides, and oxygen consumption when first introduced into salt water were more evident in April and May when fish were less than 50 mm in length. In fish longer than 50 mm, the only significant differences among the stocks were in saltwater growth. Between June and August, sea-type fish showed faster growth than river-type fish which in turn grew faster than lake-type fish. When introduced into salt water in October, virtually no growth occurred in any stock, regardless of fish size. River-type and lake-type sockeye, which normally overwinter 1 and 2 yr, respectively, in freshwater, can be reared in seawater if underyearlings are raised to a length of 50 mm before release into salt water, similar to the normal life history of sea-type underyearlings. Early life history appears to be influenced more by habitat than by genetics.
Interspecific patterns of fish life histories were evaluated in relation to several theoretical models of life-history evolution. Data were gathered for 216 North American fish species (57 families) to explore relationships among variables and to ordinate species. Multivariate tests, performed on freshwater, marine, and combined data matrices, repeatedly identified a gradient associating later-maturing fishes with higher fecundity, small eggs, and few bouts of reproduction during a short spawning season and the opposite suite of traits with small fishes. A second strong gradient indicated positive associations between parental care, egg size, and extended breeding seasons. Phylogeny affected each variable, and some higher taxonomic groupings were associated with particular life-history strategies. High-fecundity characteristics tended to be associated with large species ranges in the marine environment. Age at maturation, adult growth rate, life span, and egg size positively correlated with anadromy. Parental care was inversely correlated with median latitude. A trilateral continuum based on essential trade-offs among three demographic variables predicts many of the correlations among life-history traits. This framework has implications for predicting population responses to diverse natural and anthropogenic disturbances and provides a basis for comparing responses of different species to the same disturbance.
SUMMARYThe range of hosts used by a parasite is influenced by macro-evolutionary processes (host switching, host–parasite co-evolution), as well as ‘encounter filters’ and ‘compatibility filters’ at the micro-evolutionary level driven by host/parasite ecology and physiology. Host specialization is hypothesized to result in trade-offs with aspects of parasite life history (e.g. reproductive output), but these have not been well studied. We used previously published data to create models examining general relationships among host specificity and important aspects of life history and reproduction for nematodes parasitizing animals. Our results indicate no general trade-off between host specificity and the average pre-patent period (time to first reproduction), female size, egg size, or fecundity of these nematodes. However, female size was positively related to egg size, fecundity, and pre-patent period. Host compatibility may thus not be the primary determinant of specificity in these parasitic nematodes if there are few apparent trade-offs with reproduction, but rather, the encounter opportunities for new host species at the micro-evolutionary level, and other processes at the macro-evolutionary level (i.e. phylogeny). Because host specificity is recognized as a key factor determining the spread of parasitic diseases understanding factors limiting host use are essential to predict future changes in parasite range and occurrence.
Daily egg production of the moth Parapediasia teterrella declined over the life-span of the female but egg size remained constant. The absence of water resulted in lower fecundity and early mortality. Egg size and lifetime fecundity showed considerable inter-individual variation and large females produced more and larger eggs than their smaller counterparts. Large females expended greater reproductive effort than small females. Hatching success was negatively related to egg size. In spite of this, large females laying large eggs had higher fitness than small females. I postulate that multiple reproductive strategies within a species, resulting from differences in reproductive effort expended, may explain why expected trade-offs in reproductive parameters (e.g., egg size versus egg number) were not found in this species. Furthermore, I argue that the prevalent interpretation of life-history evolution (that body size is the important determining parameter of life-history parameters) may reflect correlation of body size with reproductive effort, and reproductive effort may be more important in determining the nature of trade-offs between reproductive parameters.
Anadromous (sockeye salmon) and nonanadromous (kokanee) Oncorhynchus nerka spawn sympatrically yet appear genetically distinct in a number of rivers in British Columbia. To investigate whether genetic differences are maintained by selection against -hybrid" progeny, we raised pure and reciprocal crosses of Shuswap River sockeye and kokanee under controlled hatchery conditions. Sockeye eggs were larger and survived slightly better than kokanee eggs, regardless of male type, both to the eyed egg stage and as young fry. We observed no differences in survival among cross types during the remainder of the 460 d study. Rate of yolk absorption was similar in pure sockeye and pure kokanee alevins, but significantly faster in alevins sired by sockeye than those sired by kokanee. This indicates a male genetic effect which compensates for the difference in egg size. Hybrid alevins developed differently because egg size is mismatched with the male genotype. Growth rates of fry were significantly more variable within pure kokanee families than within pure sockeye families Hybrid crosses survived as well as pure crosses under the study conditions. However, any progeny resulting from hybrid crosses in nature may sustain higher mortality than those from pure crosses.
Eggs spawned naturally by 3,883 females in 1925 were estimated as amounting to 17,470,000. Approximately 12,500 fry (0.07% of eggs) migrated to sea in 1926, 183,272 yearlings (1.05%) in 1927, and 1,722 two-year-olds (0.01%) in 1928, making 1.13% in all. Returning fish consisted of no three-year (32 group), 4,463 four-year (42 group), and 1,112 five-year fish (no 52 group, all being of the 53 group). None of the fish was reported returning to other spawning areas.
This study compared fecundity-length-latitude relationships between 25 kokanee populations (15 natural and 10 introduced) and 48 sockeye salmon populations. Significant differences confirmed the hypothesis that the two Oncorhynchus nerka variants follow different reproductive strategies: (i) fecundity is more highly correlated with length for kokanee than for sockeye salmon; (ii) kokanee have higher fecundity-length regression slopes and lower intercepts than sockeye salmon; (iii) kokanee populations share a common fecundity-length regression slope, but sockeye salmon populations do not; and (iv) average lengths and fecundities of kokanee decrease with increasing latitude, but those of sockeye salmon do not. The first three findings confirm that kokanee maintain a constant egg size while increasing egg number with increasing body size but that sockeye salmon increase both egg number and egg size with increasing body size. Kokanee egg sizes may be less variable than those of sockeye salmon because kokanee have lower and less variable energetic costs of spawning migration and tend to use spawning gravel with smaller and less variable particle sizes. Latitudinal clines in kokanee length and fecundity may reflect latitudinal gradients in temperature and duration of the growing season. Such environmental gradients may explain why kokanee populations are rarely found as far north as Alaska.
Genome‐wide analysis reveals demographic and life‐history patterns associated with habitat modification in landlocked, deep‐spawning sockeye salmon (
Oncorhynchus nerka
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