scholarly journals Correlated contemporary evolution of life history traits in New Zealand Chinook salmon, Oncorhynchus tshawytscha

Heredity ◽  
2011 ◽  
Vol 106 (3) ◽  
pp. 448-459 ◽  
Author(s):  
M T Kinnison ◽  
T P Quinn ◽  
M J Unwin
1997 ◽  
Vol 54 (6) ◽  
pp. 1235-1245 ◽  
Author(s):  
M J Unwin ◽  
G J Glova

Chinook salmon (Oncorhynchus tshawytscha) spawning runs in Glenariffe Stream, New Zealand, exhibited significant changes in life history traits following supplementation releases of hatchery-reared juveniles. Total run strength did not change but the proportion of naturally produced fish declined to 34%. Attempts to separate spawners of natural and hatchery origin were unsuccessful, and 31-48% of natural spawners are now of hatchery origin. Hatchery males were smaller at age 2 and 3 than males of natural origin, and more often matured as jacks, producing an 86-mm decrease in mean fork length over 28 years. There was no change in length at age or age at maturity for female spawners. The proportion of jacks entering Glenariffe Stream each year was positively correlated with the proportion of jacks in the ensuing cohort. Most differences between fish of natural and hatchery origin were related to hatchery rearing practices, but the decline in age at maturity among naturally produced males appears to reflect traits inherited from parent stock of hatchery origin. Hatchery releases may also favour the survival of ocean-type fry over stream-type fry, possibly reversing a tendency for stream-type behaviour to evolve in response to the lack of estuaries on most New Zealand chinook salmon rivers.


1993 ◽  
Vol 50 (7) ◽  
pp. 1414-1421 ◽  
Author(s):  
Thomas P. Quinn ◽  
Martin J. Unwin

Chinook salmon (Oncorhynchus tshawytscha) were introduced to New Zealand, apparently from a single California population, and have been self-sustaining since about 1905. Salmon from the Waimakariri, Rakaia, Rangitata, and Waitaki rivers differed in various life history traits. The proportion of stream-type adults ranged from 29.1 to 75.6% in Rakaia and Waimakariri tributaries, respectively. Average age at maturity not only differed among the major rivers but also between two tributaries within the Rakaia River catchment. Length at age varied among rivers, the differences being most pronounced in older fish. Age structure and size at age combined to produce 91-, and 73-mm differences in mean length of males and females, respectively, among populations. Waitaki River salmon were not only long at age but also heavier for their length than other populations. The timing of entry into freshwater varied by over 1 mo between the Rakaia and Waitaki rivers, and median date of arrival on spawning grounds varied by 16 d between Rakaia and Waimakariri river tributaries. These life history traits are influenced, to varying degrees, by genetic and environmental factors. However, the suite of differences indicates that considerable adaptation to local conditions has occurred in about 20 generations.


Author(s):  
Jeffrey A. Hutchings

Life histories describe how genotypes schedule their reproductive effort throughout life in response to factors that affect their survival and fecundity. Life histories are solutions that selection has produced to solve the problem of how to persist in a given environment. These solutions differ tremendously within and among species. Some organisms mature within months of attaining life, others within decades; some produce few, large offspring as opposed to numerous, small offspring; some reproduce many times throughout their lives while others die after reproducing just once. The exponential pace of life-history research provides an opportune time to engage and re-engage new generations of students and researchers on the fundamentals and applications of life-history theory. Chapters 1 through 4 describe the fundamentals of life-history theory. Chapters 5 through 8 focus on the evolution of life-history traits. Chapters 9 and 10 summarize how life-history theory and prediction has been applied within the contexts of conservation and sustainable exploitation. This primer offers an effective means of rendering the topic accessible to readers from a broad range of academic experience and research expertise.


Evolution ◽  
2020 ◽  
Vol 74 (4) ◽  
pp. 764-774 ◽  
Author(s):  
Animesh Gupta ◽  
Anechelle N. Soto ◽  
Sarah J. Medina ◽  
Katherine L. Petrie ◽  
Justin R. Meyer

NIR news ◽  
2018 ◽  
Vol 29 (5) ◽  
pp. 12-14
Author(s):  
Matthew R Miller ◽  
Jonathan Puddick ◽  
Jane E Symonds ◽  
Seumas P Walker ◽  
Hong (Sabrina) Tian

Near infrared spectroscopy has been employed to determine the proximate composition of Chinook salmon ( Oncorhynchus tshawytscha) and Greenshell Mussels™ ( Perna canaliculus). This work was presented at the Australian Near Infrared Spectroscopy Group and New Zealand Near Infrared Spectroscopy Society meeting in Rotorua, 11–12 April 2018, where it won the best overall presentation award for Near Infrared Science (Figure 1).


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