The energy cost of free existence for Bering Sea Harbor and spotted seals
Dissertation (Ph.D.) University of Alaska Fairbanks, 1981 Energy-flow models were developed to assess the net and gross energy requirements of natural populations of Bering Sea harbor seals (Phoca vitulina richardsi) and spotted seals (Phoca largha), and to estimate their impact on two commercially-...
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ftunivalaska:oai:scholarworks.alaska.edu:11122/7443 2023-05-15T15:43:41+02:00 The energy cost of free existence for Bering Sea Harbor and spotted seals Ashwell-Erickson, Susan M. 1981-09 http://hdl.handle.net/11122/7443 en_US eng http://hdl.handle.net/11122/7443 Dissertation phd 1981 ftunivalaska 2023-02-23T21:36:50Z Dissertation (Ph.D.) University of Alaska Fairbanks, 1981 Energy-flow models were developed to assess the net and gross energy requirements of natural populations of Bering Sea harbor seals (Phoca vitulina richardsi) and spotted seals (Phoca largha), and to estimate their impact on two commercially-important fishes, walleye pollock (Theragra chalcogramma) and Pacific herring (Clupea harengus pallasi). Energy requirements were estimated from long-term studies of food consumption and proximate composition, food energy content and digestibility, and metabolic effects of temperature, feeding, activity, molt, and reproduction in captive representatives of each species. Captive seals adjusted their ad libitum intake of food to maintain caloric equivalence between diets of varying fat content. The mean digestible energy of pollock and herring was 96.7 ± 0.2% and 91.2 ± 0.7% of gross ingested energy, respectively, and the estimated net energy available from both diets was 80.3% of gross energy. Basal metabolism of both seal species remained constant with season and declined with age. Maximal metabolic effort in water was achieved with harbor seals carrying 8-kg weight load at an oxygen consumption rate of 32.8 ± 2.8 ml 0₂/kg·min, or approximately four times basal rate. Metabolism during molt in harbor seals was about 19% less than pre-molt levels, accompanied by a rise in plasma cortisol and decline in plasma thyroxine. Reproductive energy costs were estimated at 2.5 x 10⁵ and 2.2 x 10⁵ kcal for individual harbor and spotted seals, respectively. The annual gross energy required by both populations combined was estimated at 6.6 x 10¹¹ kcal, corresponding to an annual consumption of 8.16 x 10⁴ metric tons of pollock, 5.17 x 10⁴ metric tons of capelin (Mallotus villosus), 3.74 x 10⁴ metric tons of herring, and 4.61 x 10⁴ metric tons of invertebrate species, four important prey of seals. These results suggest that the annual pollock and herring intake of both populations may be about 9% and 20%, respectively, of the ... Doctoral or Postdoctoral Thesis Bering Sea Phoca vitulina Theragra chalcogramma Alaska University of Alaska: ScholarWorks@UA Bering Sea Fairbanks Pacific |
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University of Alaska: ScholarWorks@UA |
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English |
description |
Dissertation (Ph.D.) University of Alaska Fairbanks, 1981 Energy-flow models were developed to assess the net and gross energy requirements of natural populations of Bering Sea harbor seals (Phoca vitulina richardsi) and spotted seals (Phoca largha), and to estimate their impact on two commercially-important fishes, walleye pollock (Theragra chalcogramma) and Pacific herring (Clupea harengus pallasi). Energy requirements were estimated from long-term studies of food consumption and proximate composition, food energy content and digestibility, and metabolic effects of temperature, feeding, activity, molt, and reproduction in captive representatives of each species. Captive seals adjusted their ad libitum intake of food to maintain caloric equivalence between diets of varying fat content. The mean digestible energy of pollock and herring was 96.7 ± 0.2% and 91.2 ± 0.7% of gross ingested energy, respectively, and the estimated net energy available from both diets was 80.3% of gross energy. Basal metabolism of both seal species remained constant with season and declined with age. Maximal metabolic effort in water was achieved with harbor seals carrying 8-kg weight load at an oxygen consumption rate of 32.8 ± 2.8 ml 0₂/kg·min, or approximately four times basal rate. Metabolism during molt in harbor seals was about 19% less than pre-molt levels, accompanied by a rise in plasma cortisol and decline in plasma thyroxine. Reproductive energy costs were estimated at 2.5 x 10⁵ and 2.2 x 10⁵ kcal for individual harbor and spotted seals, respectively. The annual gross energy required by both populations combined was estimated at 6.6 x 10¹¹ kcal, corresponding to an annual consumption of 8.16 x 10⁴ metric tons of pollock, 5.17 x 10⁴ metric tons of capelin (Mallotus villosus), 3.74 x 10⁴ metric tons of herring, and 4.61 x 10⁴ metric tons of invertebrate species, four important prey of seals. These results suggest that the annual pollock and herring intake of both populations may be about 9% and 20%, respectively, of the ... |
format |
Doctoral or Postdoctoral Thesis |
author |
Ashwell-Erickson, Susan M. |
spellingShingle |
Ashwell-Erickson, Susan M. The energy cost of free existence for Bering Sea Harbor and spotted seals |
author_facet |
Ashwell-Erickson, Susan M. |
author_sort |
Ashwell-Erickson, Susan M. |
title |
The energy cost of free existence for Bering Sea Harbor and spotted seals |
title_short |
The energy cost of free existence for Bering Sea Harbor and spotted seals |
title_full |
The energy cost of free existence for Bering Sea Harbor and spotted seals |
title_fullStr |
The energy cost of free existence for Bering Sea Harbor and spotted seals |
title_full_unstemmed |
The energy cost of free existence for Bering Sea Harbor and spotted seals |
title_sort |
energy cost of free existence for bering sea harbor and spotted seals |
publishDate |
1981 |
url |
http://hdl.handle.net/11122/7443 |
geographic |
Bering Sea Fairbanks Pacific |
geographic_facet |
Bering Sea Fairbanks Pacific |
genre |
Bering Sea Phoca vitulina Theragra chalcogramma Alaska |
genre_facet |
Bering Sea Phoca vitulina Theragra chalcogramma Alaska |
op_relation |
http://hdl.handle.net/11122/7443 |
_version_ |
1766377878932422656 |