Estimations of Ocean Mortality Rates for Pacific Salmon (Oncorhynchus)

1962 ◽  
Vol 19 (4) ◽  
pp. 561-589 ◽  
Author(s):  
Robert R. Parker
Keyword(s):  
Mortality Rate ◽  
Sockeye Salmon ◽  
Pacific Salmon ◽  
Pink Salmon ◽  
Total Mortality ◽  
Mortality Rates ◽  
Mortality Factor ◽  
Sampling Errors ◽  
Instantaneous Rate ◽  
Factor C

A conceptual model representing natural marine mortality rates of Pacific salmon is developed. Ocean mortality rate (q) is taken as the base to which coastal mortality rates of juveniles (c) and of adults (k) are additive factors. The effect of marking is taken as a multiplicative factor (m) of the instantaneous rate (i) where i = q + c + k. Together with time these values are incorporated into the balanced equation[Formula: see text]where N0 denotes the population entering the sea and R1, R2, R3 denote the returns at succeeding times of maturity. The locus of c + k = f(q) is used to graphically depict all possible combinations of c + k and q within the limits [q, c + k = 0]. Intersections of loci are taken as estimates of values of q and c + k which satisfy two sets of data. Available data for sockeye salmon (O. nerka) from Cultus Lake, Chilko Lake and Hooknose Creek, British Columbia, Karluk River and Bare Lake, Alaska, and Dalnee River, Kamchatka, pink salmon (O. gorbuscha) and chum salmon (O. keta) from Hooknose Creek, chinook salmon (O. tshawytscha) from the coast of Southeast Alaska and coho (O. kisutch) from the Eel River, California, are utilized. It is concluded that ocean mortality is relatively constant, of the order of magnitude q = 0. 32 or S = 73% annually. A juvenile coastal mortality factor (c) apparently exists and is characteristic of the species and race through the media of size of migrants, time spent in the costal area, and geography. An adult coastal factor (k) may exist but is of negligible influence on the total mortality rate. While the data utilized collectively may be considered as extensive, serious defects in sampling errors and undefined variability were encountered. It is doubted that mortality rates can be more accurately defined from any repetition of experiments used, hence a more direct approach is indicated for solution of this problem.

scholarly journals Pacific salmon abundance trends and climate change

2011 ◽  
Vol 68 (6) ◽  
pp. 1122-1130 ◽  
Author(s):  
James R. Irvine ◽  
Masa-aki Fukuwaka
Keyword(s):  
Climate Change ◽  
Pacific Ocean ◽  
North Pacific ◽  
Sockeye Salmon ◽  
Coho Salmon ◽  
Pacific Salmon ◽  
North Pacific Ocean ◽  
Pink Salmon ◽  
The North ◽  
Abundance Trends

Abstract Irvine, J. R., and Fukuwaka, M. 2011. Pacific salmon abundance trends and climate change. – ICES Journal of Marine Science, 68: 1122–1130. Understanding reasons for historical patterns in salmon abundance could help anticipate future climate-related changes. Recent salmon abundance in the northern North Pacific Ocean, as indexed by commercial catches, has been among the highest on record, with no indication of decline; the 2009 catch was the highest to date. Although the North Pacific Ocean continues to produce large quantities of Pacific salmon, temporal abundance patterns vary among species and areas. Currently, pink and chum salmon are very abundant overall and Chinook and coho salmon are less abundant than they were previously, whereas sockeye salmon abundance varies among areas. Analyses confirm climate-related shifts in abundance, associated with reported ecosystem regime shifts in approximately 1947, 1977, and 1989. We found little evidence to support a major shift after 1989. From 1990, generally favourable climate-related marine conditions in the western North Pacific Ocean, as well as expanding hatchery operations and improving hatchery technologies, are increasing abundances of chum and pink salmon. In the eastern North Pacific Ocean, climate-related changes are apparently playing a role in increasing chum and pink salmon abundances and declining numbers of coho and Chinook salmon.

Protandry in Pacific salmon

2000 ◽  
Vol 57 (6) ◽  
pp. 1252-1257 ◽  
Author(s):  
Yolanda Morbey
Keyword(s):  
Chinook Salmon ◽  
Sockeye Salmon ◽  
Coho Salmon ◽  
Pacific Salmon ◽  
Pink Salmon ◽  
Statistical Procedure ◽  
Timing Data ◽  
Mating Opportunities ◽  
Gender Specific ◽  
Specific Timing

Protandry, the earlier arrival of males to the spawning grounds than females, has been reported in several studies of Pacific salmon (Oncorhynchus spp.). However, the reasons for protandry in salmon are poorly understood and little is known about how protandry varies among and within populations. In this study, protandry was quantified in a total of 105 years using gender-specific timing data from seven populations (one for pink salmon (O. gorbuscha), three for coho salmon (O. kisutch), two for sockeye salmon (O. nerka), and one for chinook salmon (O. tshawytscha)). Using a novel statistical procedure, protandry was found to be significant in 90% of the years and in all populations. Protandry may be part of the males' strategy to maximize mating opportunities and may facilitate mate choice by females.

scholarly journals Climate and competition influence sockeye salmon population dynamics across the Northeast Pacific Ocean

2020 ◽  
Vol 77 (6) ◽  
pp. 943-949 ◽  
Author(s):  
Brendan Connors ◽  
Michael J. Malick ◽  
Gregory T. Ruggerone ◽  
Pete Rand ◽  
Milo Adkison ◽  
...  
Keyword(s):  
Sockeye Salmon ◽  
Large Scale ◽  
Pacific Salmon ◽  
Spatial Scales ◽  
Interspecific Interactions ◽  
Pink Salmon ◽  
Oncorhynchus Gorbuscha ◽  
Negative Effects ◽  
Positive Effects ◽  
The North

Pacific salmon productivity is influenced by ocean conditions and interspecific interactions, yet their combined effects are poorly understood. Using data from 47 North American sockeye salmon (Oncorhynchus nerka) populations, we present evidence that the magnitude and direction of climate and competition effects vary over large spatial scales. In the south, a warm ocean and abundant salmon competitors combined to strongly reduce sockeye productivity, whereas in the north, a warm ocean substantially increased productivity and offset the negative effects of competition at sea. From 2005 to 2015, the approximately 82 million adult pink salmon (Oncorhynchus gorbuscha) produced annually from hatcheries were estimated to have reduced the productivity of southern sockeye salmon by ∼15%, on average. In contrast, for sockeye at the northwestern end of their range, the same level of hatchery production was predicted to have reduced the positive effects of a warming ocean by ∼50% (from a ∼10% to a ∼5% increase in productivity, on average). These findings reveal spatially dependent effects of climate and competition on sockeye productivity and highlight the need for international discussions about large-scale hatchery production.

Abstract P159: No Gender Difference in All-Cause Mortality Rates in a Cohort of Heart Failure With Preserved Ejection Fraction in the US Veteran Population

Circulation ◽  
2018 ◽  
Vol 137 (suppl_1) ◽  
Author(s):  
Katherine E Kurgansky ◽  
David Gagnon ◽  
Kelly Cho ◽  
J M Gaziano ◽  
Jacob Joseph ◽  
...  
Keyword(s):  
Heart Failure ◽  
Mortality Rate ◽  
Ejection Fraction ◽  
Rate Ratio ◽  
Total Mortality ◽  
Mortality Rates ◽  
Failure Diagnosis ◽  
Preserved Ejection Fraction ◽  
Heart Failure Diagnosis

Introduction: Heart failure with preserved ejection fraction (HFpEF) affects about 5% of people 65 or older, with a higher prevalence in women. Previous studies suggest that women with HFpEF may live longer than men. Further understanding of mortality outcomes by gender could be useful in implementing gender-specific treatment strategies to improve outcomes in HFpEF patients. Hypothesis: We assessed the hypothesis that women have a lower rate of total mortality than males in a US Veteran HFpEF cohort. Methods: We used a validated algorithm to curate a HFpEF cohort using ICD9 codes, laboratory values, medications, and ejection fraction values from the national Veterans Affairs database. This algorithm had 88% sensitivity and 96% specificity. We examined crude and adjusted mortality rates by gender, beginning at the time of heart failure diagnosis with follow-up through 2016. The adjusted mortality rate was directly standardized to the population of veterans with heart failure (n= 626,179) according to distribution of age, race, cardiovascular disease (CVD), and chronic kidney disease (CKD). Crude and standardized rate ratios were calculated from the mortality rates. Results: Our HFpEF cohort (n= 74,937) included 72,267 men and 2,670 women. Mean age was 72.5 (11.2) in men and 69.1 (14.3) in women at the time of heart failure diagnosis. Males were 85.2% white, 33.7% had CVD, and 27.1% had CKD, whereas females were 82.5% white, 28.7% had CVD, and 20.5% had CKD. During a mean follow up of 4.8 (3.7) years, 52,703 deaths occurred in men and 1,614 deaths occurred in women.The crude mortality rate was significantly lower for females (109.7/1000 person-years) compared to males (153.5/1000 person-years). Corresponding crude incidence rate ratio (95% CI) for total mortality comparing females to males was 0.71 (0.69-0.74; p<.0001). However, after standardizing, there was no significant difference in total mortality rates between men (170.0/1000 person-years) and women (173.4/1000 person-years). The standardized mortality rate ratio was 1.02 (95% CI: 0.84-1.23; p=0.8397). Conclusions: In conclusion, our data do not show any difference in total mortality rate between men and women following the diagnosis of HFpEF.

Homing behavior and vertical movements of four species of Pacific salmon (Oncorhynchus spp.) in the central Bering Sea

1995 ◽  
Vol 52 (3) ◽  
pp. 532-540 ◽  
Author(s):  
Miki Ogura ◽  
Yukimasa Ishida
Keyword(s):  
Chinook Salmon ◽  
Bering Sea ◽  
Sockeye Salmon ◽  
Pacific Salmon ◽  
Pink Salmon ◽  
Depth Sensing ◽  
Compass Orientation ◽  
Homing Behavior ◽  
Vertical Movements ◽  
Strong Surface

Four sockeye salmon (Oncorhynchus nerka), two chum salmon (O. keta), three pink salmon (O. gorbuscha), and four Chinook salmon (O. tshawytscha) with depth-sensing ultrasonic transmitters were tracked in the central Bering Sea to examine migration in the open sea. Ground speeds of maturing sockeye, chum, and pink salmon were at 0.54–0.66 m/s (0.88–1.17 fork lengths/s). Chinook salmon, probably immature fish, moved more slowly (0.34 m/s). Maturing individuals moved in particular directions and maintained their ground speeds and directions during day and night. The results also suggested that salmon had a compass orientation ability functioning without celestial information. Sockeye, chum, and pink salmon showed strong surface preferences but chinook salmon swam deeper (30–35 m) than did the other species.

Effect of incubation temperature on the development of five species of Pacific salmon (Oncorhynchus) embryos and alevins

1988 ◽  
Vol 66 (1) ◽  
pp. 266-273 ◽  
Author(s):  
C. B. Murray ◽  
J. D. McPhail
Keyword(s):  
Chinook Salmon ◽  
Sockeye Salmon ◽  
Coho Salmon ◽  
Incubation Temperature ◽  
Pacific Salmon ◽  
Pink Salmon ◽  
Oncorhynchus Gorbuscha ◽  
Embryo Survival ◽  
Salmon Fry ◽  
Incubation Temperatures

Embryo and alevin survival, time to hatching and emergence, and alevin and fry size of five species of Pacific salmon (Oncorhynchus) were observed at five incubation temperatures (2, 5, 8, 11, and 14 °C). No pink (Oncorhynchus gorbuscha) or chum (O. keta) salmon embryos survived to hatching at 2 °C. Coho (O. kisutch) and sockeye (O. nerka) salmon had higher embryo survival at 2 °C than chinook (O. tschawytscha) salmon. At 14 °C, chum, pink, and chinook salmon had higher embryo survival than coho or sockeye salmon. In all species, peaks of embryo mortality occurred at specific developmental stages (completion of epiboly, eye pigmentation, and hatching). Alevin survival to emergence was high for all species, except for coho and pink salmon at 14 °C. Hatching and emergence time varied inversely with incubation temperature, but coho salmon hatched and emerged sooner at all temperatures than the other species. Coho and sockeye salmon alevins were larger at 2 °C, pink, chum, and chinook salmon alevins were larger at 5 and 8 °C. Coho salmon fry were larger at 2 °C, chinook and chum salmon fry were larger at 5 °C, and sockeye and pink salmon fry were larger at 8 °C. High incubation temperatures reduced fry size in all species. Each species of Pacific salmon appears to be adapted to different spawning times and temperatures, and thus indirectly to specific incubation temperatures, to ensure maximum survival and size and to maintain emergence at the most favorable time each year.

scholarly journals Growth, maturation, and longevity of maturation cohorts of Norwegian spring-spawning herring

2004 ◽  
Vol 61 (2) ◽  
pp. 165-175 ◽  
Author(s):  
Raymond J.H. Beverton ◽  
Arvid Hylen ◽  
Ole-Johan Østvedt ◽  
John Alvsvaag ◽  
Terence C. Iles
Keyword(s):  
Mortality Rate ◽  
Small Proportion ◽  
Stock Assessment ◽  
Adult Life ◽  
Total Mortality ◽  
Mortality Rates ◽  
Natural Mortality ◽  
Marine Research ◽  
First Time ◽  
Age At Maturation

Abstract In 1907, the Bergen Institute of Marine Research started regular sampling of scales and lengths from landings of mature Norwegian spring-spawning herring. The actual age of each fish when caught was recorded, and from the early 1920s also the age at which it spawned for the first time. The present analyses concern biological samples secured during the fishing seasons 1940–1964. Herring in this stock do not all reach maturity at the same age. A small proportion of any one year class matures at 3 years. The majority matures from the age of 4–7 years, and a small proportion of some year classes at 8 and even 9 years of age. Subsequent age composition and growth of each maturation cohort were followed throughout mature life after spawning for the first time. The maximum age was found to increase with age at maturation, rising to an asymptote of about 22 years. The von Bertalanffy parameter L∞ shows an increasing trend with age at maturation, while K decreases. There is no strict length threshold at maturation and the curve joining the length at which each maturation cohort reaches maturity is less steep than the growth curve itself over the range of maturation ages. The data suggest that fish in this stock spawn, on average, eight times during a period of their life history in which the mortality rate is independent of age. After these eight spawnings, at an age referred to in this paper as the hinge age, the mortality rate increases sharply. Thus, the adult life is divided into two phases, called here pre-senescent and senescent. The total mortality rates in the pre-senescent phase are relatively stable for all maturation cohorts 3–9, but there is some evidence of a trend towards higher mortality rates during the senescent phase for the youngest maturing fish. This trend is caused mainly by a reduced natural mortality in the fish that mature when older. These findings have interesting demographic implications. Additional mortality due to fishing will change the relative contribution of young and old maturation cohorts in the senescent phase, thus making it appear that natural mortality is dependent on the intensity of fishing. Consequently, for stock assessment, analysis on a cohort basis seems advisable.

Evaluation of a simple technique for recovering fish from capture stress: integrating physiology, biotelemetry, and social science to solve a conservation problem

2013 ◽  
Vol 70 (1) ◽  
pp. 90-100 ◽  
Author(s):  
M.R. Donaldson ◽  
G.D. Raby ◽  
V.N. Nguyen ◽  
S.G. Hinch ◽  
D.A. Patterson ◽  
...  
Keyword(s):  
Social Science ◽  
Sockeye Salmon ◽  
Pacific Salmon ◽  
Pink Salmon ◽  
Oncorhynchus Gorbuscha ◽  
Plasma Sodium ◽  
Low Velocity ◽  
Air Exposure ◽  
Positive Attitudes ◽  
Capture Stress

We evaluate the utility of an inexpensive, portable recovery bag designed to facilitate recovery of fish from capture stress by combining physiological assays, biotelemetry, and social science surveys. Adult migrating Pacific salmon (Oncorhynchus spp.) were used as a model, since some of their populations are threatened. While catch-and-release is common, there is a need to ensure that it is sustainable. A social science survey revealed that anglers generally have positive attitudes towards recovery bag use, particularly if research identifies that such techniques could be effective. Physiological assays on pink salmon (Oncorhynchus gorbuscha) revealed benefits of both high- and low-velocity recovery, but high velocity was most effective with reduced plasma cortisol concentrations and similar plasma sodium and chloride concentrations as those found in controls at all recovery durations. A biotelemetry study on sockeye salmon (Oncorhynchus nerka) captured by anglers and stressed by air exposure then placed in recovery bags had 20% higher, but not significantly different, survival than no-recovery salmon. The integration of natural science and social science provides an important step forward in developing methods for promoting recovery of fish from capture.

Estimation of Sea Mortality Rates for the 1960 Brood-Year Pink Salmon of Hook Nose Creek, British Columbia

1964 ◽  
Vol 21 (5) ◽  
pp. 1019-1034 ◽  
Author(s):  
Robert R. Parker
Keyword(s):  
British Columbia ◽  
Mortality Rate ◽  
Marine Environment ◽  
Pink Salmon ◽  
Mortality Rates ◽  
Natural Mortality ◽  
Two Stage ◽  
Fishing Season ◽  
Salmon Fry ◽  
Bella Coola

Seaward migrating pink salmon fry at Hook Nose Creek, British Columbia, were estimated to total 1,153,000 in 1961. Of these, 41.5% or 479,000, were marked by amputation of both ventral fins (BV). Following this marking 36,900 fingerling were captured in the marine environment and marked by removal of the adipose and right ventral fins (ARV). During the 1962 fishing season 1,160,645 adult pinks were examined and 7050 BV and 184 ARV marks recognized. For the Hook Nose Creek stock, survival at sea from natural causes is shown to approximate 22% and the rate of exploitation was 95%. This stock is shown to be more exposed to fishing than the Bella Coola stock, for which a rate of exploitation of 69–80% is estimated. Rate of exploitation for Dean Channel stocks is even lower. These differences are explained as due to times of entry and rates of travel through the fishery. The two-stage marking experiment failed to estimate the natural mortality rate of juvenile pinks during the initial 5 weeks of sea life because of this dissimilarity between rates of exploitation on the stocks in the area.

scholarly journals Estimation of air pollution influence on demographic and health of the population of Saratov

2016 ◽  
Vol 5 (4) ◽  
pp. 65-70
Author(s):  
Natalya Vitalievna Tochilkina
Keyword(s):  
Air Pollution ◽  
Mortality Rate ◽  
Nitrogen Oxide ◽  
Respiratory Diseases ◽  
Total Mortality ◽  
Mortality Rates ◽  
Complex Index ◽  
Full Analysis ◽  
One Year ◽  
The Impact

The article examines the impact of air pollution on the demographic characteristics of the residents of Saratov. It describes the main air pollutants that have a significant impact on the incidence of non-communicable diseases and child mortality. The author discusses the impact of complex index of air pollution and its components on overall mortality rates, mortality from cancer, respiratory diseases and the mortality rate of children under one year. The research has shown that there is a strong direct relationship between the complex index of air pollution and mortality from respiratory diseases and infant mortality rates. The author also reveals that the total mortality rate is closely associated with the increased content in the air of nitrogen oxide, the mortality rate from cancer with the increased content of nitrogen oxide and phenol, the mortality rate from respiratory diseases with excess of formaldehyde, the mortality rate of children under one year - with excess of formaldehyde and phenol. Despite the importance and relevance of such studies the author notes that it is difficult to access the information about morbidity by classes of diseases, by age and sex of the inhabitants of various administrative areas of the city. It does not enable a full analysis of the current situation and retrospective studies for its prediction.

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