Thyroid Hormone Content of Eggs and Early Developmental Stages of Five Oncorhynchus Species

1989 ◽  
Vol 46 (12) ◽  
pp. 2140-2145 ◽  
Author(s):  
J. F. Leatherland ◽  
L. Lin ◽  
N. E. Down ◽  
E. M. Donaldson
Keyword(s):  
Chinook Salmon ◽  
Sockeye Salmon ◽  
Chum Salmon ◽  
Developmental Stages ◽  
Coho Salmon ◽  
Pink Salmon ◽  
Detectable Range ◽  
Early Developmental Stages ◽  
Low Levels ◽  
Early Developmental

Measurements were made of thyroxine (T4) and triiodothyronine (T3) levels in the embryos and larvae of five species of the genus Oncorhynchus. Pink salmon (O. gorbuscha) embryos and larvae contained relatively low levels of both T4 and T3 throughout the early developmental stages. Sockeye salmon (O. nerka) had the highest levels of T4, with coho (O. kisutch), chum (O. keta), and chinook salmon (O. tshawytscha) having similar total T4 content. The chinook salmon embryos contained the highest T3 content of the five species studied, pink, sockeye, and chum salmon embryos had relatively low levels, and coho salmon embryos had intermediate levels of T3. In the pink salmon, there was little evidence of significant change in either T4 or T3 during development. In the other four species, the T4 content changed little between fertilization and hatch, but fell thereafter to stabilize at levels close to the lower detectable range of the assay used, except in the sockeye salmon larvae in which the values were considerably higher. The T3 content of chinook and coho salmon changed with development in a manner comparable with that observed for T4, but there was little evidence of a comparable posthatch decline in T3 levels in chum, sockeye, or pink 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.

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.

Review of the Rate of Growth and Mortality of Pacific Salmon in Salt Water, and Noncatch Mortality Caused by Fishing

1976 ◽  
Vol 33 (7) ◽  
pp. 1483-1524 ◽  
Author(s):  
W. E. Ricker
Keyword(s):  
Chinook Salmon ◽  
Sockeye Salmon ◽  
Coho Salmon ◽  
Pacific Salmon ◽  
Salt Water ◽  
Pink Salmon ◽  
Total Yield ◽  
Coastal Region ◽  
Natural Mortality ◽  
Time Of Year

Mortality (other than landed catch) caused by pelagic gillnetting is estimated to be equal to the catch, for salmon in their penultimate year of life, and equal to about a quarter of the catch for salmon in their final year of life. Mortality caused by trolling for coho (Oncorhynchus kisutch) and chinook salmon (O. tshawytscha) averages about one fish killed (mostly below legal size) for every two that are boated. The natural mortality rate for sockeye salmon (O. nerka) in their final year of life averages about 0.015 per mo and is somewhat more in earlier years of pelagic life; the greater part of natural mortality after the smolt stage occurs during the downstream migration and early months of "coastal" life. For coho and chinook the best natural mortality estimate for the last year of life is 0.013 per mo, and that for pink (O. gorbuscha) and chum (O. keta) is of the same order. Growth rates during the final growing season vary from 0.26 per mo for pink and coho salmon to 0.06 per mo for chinook in their 5th ocean yr. Gains from ceasing to take immature salmon on the high seas range up to 300% of the catch now being taken in that category, while for fish taken in their final year they range up to about 70%, depending on the time of year at which the fishing is done. Gains from transferring existing pelagic net fisheries to the coastal region would be 76% (North American sockeye) and 86% (Asian sockeye) of the weight of fish now caught pelagically. Gains in total yield of existing salmon fisheries (pelagic and coastal) are estimated as 78% for Asian pink salmon and 72% for Asian sockeye. The increase in weight of the total catch from discontinuing ocean trolling for Columbia River chinook salmon and increasing river fishing correspondingly is estimated tentatively as between 63 and 98%.

The Ecology of Juvenile Salmon in the Northeast Pacific Ocean: Regional Comparisons

2007 ◽  
Keyword(s):  
Chinook Salmon ◽  
Sockeye Salmon ◽  
Coho Salmon ◽  
Pink Salmon ◽  
Gulf Of Alaska ◽  
Vancouver Island ◽  
Early Summer ◽  
Juvenile Salmon ◽  
Central California ◽  
Bottom Depth

Abstract.—In this chapter, we describe the distributions and abundances of juvenile Chinook salmon <em>Oncorhynchus tshawytscha</em>, coho salmon <em>O. kisutch</em>, chum salmon <em>O. keta</em>, pink salmon <em>O. gorbuscha</em>, and sockeye salmon <em>O. nerka </em>in six regions along the west coast of North America from central California to the northern Gulf of Alaska during the early summer (June and July) and late summer–fall (August– November) of 2000, 2002, and 2004. We also describe fish abundance in relation to bottom depth and to the average temperature and salinity of the upper water column. Salmon were collected in rope trawls from the upper 15–20 m over the open coastal shelf. Catch per unit effort was standardized across the different regions. Subyearling Chinook salmon were found only from central California to British Columbia. Yearling Chinook salmon were widespread, but were most abundant between Oregon and Vancouver Island. Juvenile coho salmon were widespread from northern California to the northern Gulf of Alaska, whereas chum, sockeye, and pink salmon were only abundant from Vancouver Island north into the Gulf of Alaska. Generally, the juveniles of the different salmon species were most abundant at, or north of, the latitudes at which the adults spawn. Abundances were particularly high near major exit corridors for fish migrating from freshwater or protected marine waters onto the open shelf. Seasonal latitudinal shifts in abundance of the juvenile salmon were generally consistent with the counterclockwise migration model of Hartt and Dell (1986). Subyearling Chinook salmon were associated with the high salinity environment found off California and Oregon, whereas chum, sockeye, and pink salmon were associated with the lower salinity environment in the Gulf of Alaska. However, within regions, evidence for strong temperature or salinity preferences among the different species was lacking. Subyearling Chinook salmon were most abundant in shallow, nearshore water.

Review of early developmental stages of trilobites and agnostids from the Barrandian area (Czech Republic)

2017 ◽  
Vol 186 (1) ◽  
pp. 103-112
Author(s):  
Lukáš Laibl ◽  
Oldřich Fatka
Keyword(s):  
Czech Republic ◽  
Developmental Stages ◽  
History Of Research ◽  
Early Developmental Stages ◽  
History Of ◽  
Barrandian Area ◽  
Early Developmental

This contribution briefly summarizes the history of research, modes of preservation and stratigraphic distribution of 51 trilobite and five agnostid taxa from the Barrandian area, for which the early developmental stages have been described.

scholarly journals The Effect of an Anthropogenic Magnetic Field on the Early Developmental Stages of Fishes—A Review

2021 ◽  
Vol 22 (3) ◽  
pp. 1210
Author(s):  
Krzysztof Formicki ◽  
Agata Korzelecka-Orkisz ◽  
Adam Tański
Keyword(s):  
Magnetic Fields ◽  
Developmental Stages ◽  
Negative Influence ◽  
Pigment Cells ◽  
Egg Activation ◽  
Industrial Equipment ◽  
Positive Effects ◽  
Early Developmental Stages ◽  
Species Specific ◽  
Early Developmental

The number of sources of anthropogenic magnetic and electromagnetic fields generated by various underwater facilities, industrial equipment, and transferring devices in aquatic environment is increasing. These have an effect on an array of fish life processes, but especially the early developmental stages. The magnitude of these effects depends on field strength and time of exposure and is species-specific. We review studies on the effect of magnetic fields on the course of embryogenesis, with special reference to survival, the size of the embryos, embryonic motor function, changes in pigment cells, respiration hatching, and directional reactions. We also describe the effect of magnetic fields on sperm motility and egg activation. Magnetic fields can exert positive effects, as in the case of the considerable extension of sperm capability of activation, or have a negative influence in the form of a disturbance in heart rate or developmental instability in inner ear organs.

scholarly journals Mitochondrial Processes during Early Development of Dictyostelium discoideum: From Bioenergetic to Proteomic Studies

Genes ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 638
Author(s):  
Monika Mazur ◽  
Daria Wojciechowska ◽  
Ewa Sitkiewicz ◽  
Agata Malinowska ◽  
Bianka Świderska ◽  
...  
Keyword(s):  
Life Cycle ◽  
Developmental Stages ◽  
Coupling Efficiency ◽  
Slime Mold ◽  
Intact Cells ◽  
Life Cycle Stages ◽  
Early Developmental Stages ◽  
Proteomic Study ◽  
And Function ◽  
Early Developmental

The slime mold Dictyostelium discoideum’s life cycle includes different unicellular and multicellular stages that provide a convenient model for research concerning intracellular and intercellular mechanisms influencing mitochondria’s structure and function. We aim to determine the differences between the mitochondria isolated from the slime mold regarding its early developmental stages induced by starvation, namely the unicellular (U), aggregation (A) and streams (S) stages, at the bioenergetic and proteome levels. We measured the oxygen consumption of intact cells using the Clarke electrode and observed a distinct decrease in mitochondrial coupling capacity for stage S cells and a decrease in mitochondrial coupling efficiency for stage A and S cells. We also found changes in spare respiratory capacity. We performed a wide comparative proteomic study. During the transition from the unicellular stage to the multicellular stage, important proteomic differences occurred in stages A and S relating to the proteins of the main mitochondrial functional groups, showing characteristic tendencies that could be associated with their ongoing adaptation to starvation following cell reprogramming during the switch to gluconeogenesis. We suggest that the main mitochondrial processes are downregulated during the early developmental stages, although this needs to be verified by extending analogous studies to the next slime mold life cycle stages.

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