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Figure 5.14 Cross and long-shelf pattern of mean density with ± 2 one standard deviation of Pinnotheridae larvae/100 m in the southeastern Bering Sea in May and June of 1978(a), 1980(b) and 1981(c). The depth interval for which means were calculated are listed above each mean in the general vicinity of their occurrence; while the range of density and the number of samples, n, collected at each interval are listed above each region. Means include both zero and positive stations. Only those depth intervals in which the number of positive samples collected is > 4 (n) are included. 678
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Outer Continental Shelf Environment
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OUTER CONTINENTAL SHELF ENVIRONMENT
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Outer Continental Shelf Environment
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TABLE OF CONTENTS List of Figures 5
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LIST OF FIGURES Figure 2.1. BIOS si
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LIST OF TABLES Table 2.1. Table 3.1
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SUMMARY Infaunal bivalve molluscs f
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FINAL REPORT on BAFFIN ISLAND EXPER
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they have little or no ability to m
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2. HYDROCARBON BIOACCUMULATION 2.1
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Table 2.1. Summary of oil concentra
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some of the oil during the period b
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Figure 2.3. Variation of aromatic h
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Figure 2.5. Mya truncata-GC 2 profi
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Figure 2.7. Aromatic profiles from
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Figure 2.9. Mya truncata aromatic p
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Figure 2.11. Mya truncata-GC 2 prof
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Figure 2.13. Concentrations of oil
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Figure 2.15. Mya truncata-Bay 11 (a
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Figure 2.17. Variation of aromatic
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Figure 2.19. Serripes groenlandicus
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Figure 2.23. Aromatic hydrocarbon p
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Figure 2.30. Astarte aromatic profi
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Figure 2.34. Aromatic hydrocarbon G
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Astarte, Bay 9, 1-day post-spill, 7
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increase in water-borne oil concent
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decision based on GC 2 . Oil levels
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profiles of tissue extracts of the
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A similar differential behavior of
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Table 3.1. Dates of collection and
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Fixed specimens from the 1981 colle
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Table 3.4. Summary of histopatholog
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Table 3.6. Summary of histopatholog
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Figure 3.1. Granulocytoma in testis
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Figure 3.5. Excessively vacuolated
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4. BIOCHEMICAL EFFECTS OF OIL The o
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Table 4.1. Carbohydrates and lipids
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Table 4.2. Concentrations of petrol
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Table 4.4. Mean concentrations of f
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In clams collected immediately befo
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Table 4.7. A summary of associated
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parameters measured. Clams from the
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alone was more gradual and reached
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interfered with feeding, gonadal de
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Brown, R.S., C.W. Brown, and S.B. S
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Malins, D.C. 1982. Alterations in t
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APPENDIX I: PANH COMPOUNDS IN OIL 1
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SPECTRUM DISPLAY/EDIT **
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** SPECTRUM DISPLAY/EDIT **
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** SPECTRUM DISPLAY/EDIT
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FILE NUMBER 12421
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XX SPECTRUM DISPLAV/EDIT **
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** SPECTRUM DISPLAVY/EDIT **
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APPENDIX III: ASTARTE BOREALIS: BAY
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** SPECTRUM DISPLAY/EDIT**
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** SPECTRUM DISPLAY/EDIT **X
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APPENDIX V: SERRIPES GROENLANDICUS:
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FEEDING ECOLOGY OF JUVENILE KING AN
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DIETARY COMPOSITION ...............
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Figure 13a. Loss of precipitin reac
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Table 10. Dietary composition of ju
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ABSTRACT To determine the food requ
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FEEDING ECOLOGY OF JUVENILE KING AN
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Figure 1.--Station locations during
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Figure 3. Station locations during
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efore freezing. From large catches
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percentage of the maximum stomach v
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The amount evacuated is given by th
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examined entered the dry weight ana
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Battelle's Pacific Northwest Divisi
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tows and trawling as techniques for
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Stomach fullness plotted against ti
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Figure 4. Decay curve for the clear
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life of the compartment. Similarly,
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Figure 6. Exponential decay curve f
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Figure 8. Exponential decay curve f
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A comparison of the equations in Ta
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hard parts with the palps and then
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Figure 10. Standardized dry weight
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Table 5. Diel feeding chronology fr
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These results are comparable to tho
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Figure 12. The frequency of newly d
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Table 7. Continued
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Table 9. Dietary composition (% fre
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Table 11. Dietary composition of ju
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Table 12. Dietary composition (% fr
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Table 14. Soft tissue to hard tissu
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Table 16. Dietary composition (% of
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polychaetes in both June and August
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Table 18. Continued 221
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and, therefore, had a caloric value
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Table 21. Caloric intake from vario
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Table 27. Results of visual examina
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They were then fed thawed juvenile
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eing tested rather than to cross re
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against its respective antigen and
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Table 29. Results of visual examina
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DISCUSSION IMMUNOASSAY The immunolo
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juvenile king crabs may depend on c
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Table 32. Comparison of August diet
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stomach contents but soft-bodied po
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The assumption that, at least for t
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shows high similiarity between the
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supply requires prediction of the s
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have been shown to readily and rapi
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Using the diel feeding chronologies
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to 70 m, potential effects from dis
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REFERENCES Addy, J. M., D. Levell,
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Hill, B. J. 1976. Natural food, for
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Tyler, A. V, 1973. Caloric values o
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CLARIFICATION All references to "se
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4.0 DISCUSSION ....................
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Figure 3.2-2 Cruise 83-3 larval red
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ACKNOWLEDGEMENTS This study was ori
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ABSTRACT The goal of this study was
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SECTION 1.0 INTRODUCTION The red ki
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1.1 Study Objectives The goal of th
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than 50 m. The oceanography of the
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entering the fishery have declined
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females. This relationship supports
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time to temperature. Time from egg-
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Juvenile crab in 2+ to 3+ age class
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BRISTOL BAY RED KING CRAB CRUISE 83
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BRISTOL BAY RED KING CRAB STATION I
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2.1.2 Field Gear and Sampling Metho
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consisted of 24 hours on all cruise
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were recorded for subsamples of lar
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200 individuals of the most common
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BRISTOL BAY RED KING CRAB STUDY ARE
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Epibenthic density and biomass data
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little vertical temperature stratif
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TABLE 3.1-1 (continued) 328
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BRISTOL BAY RED KING CRAB PERCENT G
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etween Unimak Island and Port Molle
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BRISTOL BAY RED KING CRAB SIDE-SCAN
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TABLE 3.2-1 MEAN LARVAL RED KING CR
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stations in this area where larval
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three-day period in June showed rat
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BRISTOL BAY RED KING CRAB DIEL VERT
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TABLE 3.3-1 GEOMETRIC MEAN DENSITIE
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during the June cruise (83-3). duri
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TABLE 3.4-2 NUMBER OF POST LARVAL R
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TABLE 3.4-3 NUMBER OF POST LARVAL R
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BRISTOL BAY RED KING CRAB TRYNET SA
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BRISTOL BAY RED KING CRAB TRYNET AN
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BRISTOL BAY RED KING CRAB DISTRIBUT
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NORTH ALEUTIAN BASIN RED KING CRAB
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TABLE 3.5-3 CORRELATION MATRIX FOR
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TABLE 3.5-5 CORRELATION MATRIX FOR
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at one 50 m deep TB station west of
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TABLE 3.6-2 SUMMARY OF BIOLOGICAL I
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TABLE 3.7-1 SUMMARY OF TRYNET CATCH
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group AB, especially the fish speci
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BRISTOL BAY RED KING CRAB LARVAL DE
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BRISTOL BAY RED KING CRAB LARVAL DE
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BRISTOL BAY RED KING CRAB KNOWN CIR
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Bay and west to Cape Newenham. The
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BRISTOL BAY RED KING CRAB 1978, 197
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protection against predators, as we
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which provides for adequate food (i
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4.5 Potential Effects of Oil and Ga
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to a great extent tidally driven, t
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(1983b), the same volume of oil is
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BRISTOL BAY RED KING CRAB SURFACE O
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Overt, rapid mortality of adult cra
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viability of the gametes is impaire
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detected by chemosensory organs. Pe
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and Alaskan species of shrimp and c
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interannual variability in abundanc
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that are killed by oil north of Uni
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Long-term, sublethal effects may al
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Botsford, L. and D. Wickham. 1978.
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Harris, R.P., V. Bergudugo, E.D.S.
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Kurata, H. 1961. Studies on the lar
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Paul, A.J., J. Paul, P. Shoemaker a
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Takeuchi, I. 1962, trans. 1967. On
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APPENDIX A MEAN LARVAL RED KING CRA
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APPENDIX B TRAWL GEAR TYPES USED BY
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APPENDIX C: TRAWL/DREDGE NOTES 435
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APPENDIX C (continued) 438
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Page 456 and 457:
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APPENDIX D GUT CONTENT ANALYSIS FIE
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APPENDIX D (continued) 457
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APPENDIX E: MULTIPLE LINEAR REGRESS
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APPENDIX E (continued) 462
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Page 483:
APPENDIX F: JUVENILE RED KING CRAB
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APPENDIX F (continued) Figure Fl. S
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DISTRIBUTION AND ABUNDANCE OF DECAP
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4.0 DISTRIBUTION AND ABUNDANCE OF T
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8.3 Larval Decapod Biology, Sensiti
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Figure 3.4 Figure 3.5 Figure 3.6 Fi
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Figure 5.8 Distribution and abundan
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Figure 6.29 Distribution and abunda
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Table 4.5 Table 4.6 Table 5.1 Table
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ACKNOWLEDGMENTS We are indebted to
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1.0 GENERAL INTRODUCTION 1.1 Justif
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Larval stages are generally conside
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extent in 1982) did we have the opp
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The sections of this report describ
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Table 2.1. Dates and sources of zoo
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techniques which attempt to equally
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verification of results or examinat
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cation of these larvae and the vari
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meters) was often similar (generall
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Bongo frame, the MOCNESS frame cann
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abundance within strata were made b
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520
Page 532 and 533:
522
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524
Page 536 and 537:
526
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528
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Figure 2.21 Locations and boundarie
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Figure 3.1. Location of proposed le
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characterized as part of the subarc
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Fig. 3.4. Distribution of male red
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Figure 3.5. Abundance estimates of
Page 550 and 551:
pheromone cues could impair males'
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on larvae hatched elsewhere, includ
Page 554 and 555:
aggregations could influence suscep
Page 556 and 557:
Fig. 3.7a. Distribution and relativ
Page 558 and 559:
the benthic habitat associated with
Page 560 and 561:
conclusions of Slizkin (1973) who r
Page 562 and 563:
A further observation germane to th
Page 564 and 565:
Fig. 3.10. Major king crab catch ar
Page 566 and 567:
3.4 Results 3.4.1 Distribution and
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11 and 12 (Figs. 3.11, 3.12). Too f
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Table 3.1. Number of zooplankton sa
Page 572 and 573:
Because of the poor spatial coverag
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made them imperfect in areas (Fig.
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Table 3.2. A summary of larval red
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Fig. 3.15. Distribution and relativ
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Fig. 3.16. Interannual differences
Page 582 and 583:
[An interesting note on annual abun
Page 584 and 585:
Fig. 3.17a. Frequency of occurrence
Page 586 and 587:
The occurrence of a multi-stage lar
Page 588 and 589:
megalopae. These combinations of ye
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to early August (Fig. 3.17b), and s
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Fig. 3.21. Vertical distribution of
Page 594 and 595:
consequences of oil exposure scenar
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abundance in time and space is corr
Page 598 and 599:
Female crabs were abundant in strat
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observing that: 1) the mature femal
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Much research on king crab biology
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12) Determine interannual differenc
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around the traditional king crab fi
Page 608 and 609:
Table 4.1. Historic U.S. Tanner cra
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(NMFS) since the early 1970's. In a
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Fig. 4.2b Centers of abundance of b
Page 614 and 615:
4.3 Reproduction and Description of
Page 616 and 617:
oth species for 80 mm specimens, bu
Page 618 and 619:
from all stations were pooled for v
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Fig. 4.4. Timing of appearance of l
Page 622 and 623:
Table 4.3. Timing of appearance of
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megalops larvae of both species and
Page 626 and 627:
Table 4 . 5 .Proportion of Stage II
Page 628 and 629:
Fig. 4.5. Temporal aspects of devel
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assumes a relatively homogeneous di
Page 632 and 633:
Methods for analysis of depth distr
Page 634 and 635:
Fig. 4.7. Vertical distribution of
Page 636 and 637:
were found in the upper 40 m. Eight
Page 638 and 639: From the diel stations, 10% or more
Page 640 and 641: difficulties in quantitatively samp
Page 642 and 643: Figure 4.10 Distribution and abunda
Page 644 and 645: The distribution patterns for C. ba
Page 646 and 647: 3. Most of the larval hatchout occu
Page 649 and 650: 5.0 DISTRIBUTION AND ABUNDANCE OF O
Page 651 and 652: Table 5.2. Early life history infor
Page 653 and 654: tions are not available for them. D
Page 655 and 656: to as wide as 250 mm wide by a maxi
Page 657 and 658: alutaceus larvae were collected fro
Page 659 and 660: Table 5.3. Species list of non-Chio
Page 661 and 662: annually, which resulted in little
Page 663 and 664: Figure 5.1 Vertical distribution of
Page 665 and 666: examining their vertical larval dis
Page 667 and 668: also July of 1981. Within strata, b
Page 669 and 670: Figure 5.3 Seasonal occurrence of l
Page 671 and 672: Figure 5.5 Mean density and one sta
Page 673 and 674: Long-shelf density of Erimacrus lar
Page 675 and 676: Figure 5.6 Frequency-of-occurrence
Page 677 and 678: Figure 5.7 Distribution and abundan
Page 681 and 682: Figure 5.10 Distribution of mean de
Page 683 and 684: Figure 5.12 Distribution of mean de
Page 685 and 686: at 21% of all stations sampled and
Page 687: Table 5.7. Frequency of occurrence
Page 691 and 692: 1981
Page 693 and 694: Table 5.8. Frequency of occurrence
Page 695 and 696: Figure 5.16 Mean density and one st
Page 697 and 698: Figure 5.17 Locations and densities
Page 699 and 700: Figure 5.18 Mean density and one st
Page 701 and 702: early-June; SII from early-June to
Page 703 and 704: Figure 5.19 Locations and densities
Page 705 and 706: 6.0 DISTRIBUTION AND ABUNDANCE OF S
Page 707 and 708: maturity as males at age 3.5 years
Page 709 and 710: Wigley 1969; Rasmussen 1953 from Bu
Page 711 and 712: Gulf of Maine were found to move in
Page 713 and 714: shrimp survey conducted in Unalaska
Page 715 and 716: single brood (Berkeley 1930). It is
Page 717 and 718: Table 6.2. Life history information
Page 719 and 720: Table 6.3. Life history information
Page 721 and 722: distinctive group. Most notable cha
Page 723 and 724: sampling patterns within the St. Ge
Page 725 and 726: Figure 6.2 Duration of larval stage
Page 727 and 728: Figure 6.3 Pandalus borealis stage
Page 729 and 730: June 1978 compared to June 1981. Co
Page 731 and 732: Figure 6.5 Distribution of Pandalus
Page 737 and 738: George Basin and extended over the
Page 739 and 740:
Table 6.5. Cross-shelf comparison o
Page 741 and 742:
Figure6.11 Vertical Depth Distribut
Page 743 and 744:
Page 745 and 746:
Figure 6.15 P. tridens larval abund
Page 747 and 748:
Table 6.6. Cross-shelf comparison o
Page 749 and 750:
Distribution and Abundance of Panda
Page 751 and 752:
2) While hatchout of P. borealis la
Page 753 and 754:
Page 755 and 756:
months within a single year can be
Page 757 and 758:
Figure 6.21 Hippolytidae shrimp lar
Page 759 and 760:
Figure 6.22 Vertical depth distribu
Page 761 and 762:
Page 763 and 764:
Figure6.24 Crangon spp. larval stag
Page 765 and 766:
most probably due to the mix of spe
Page 767 and 768:
Larval crangonids, Crangon spp., we
Page 769 and 770:
Page 771 and 772:
Page 773 and 774:
larval densities were generally low
Page 775 and 776:
Page 777 and 778:
Figure 6.33 Penaeid sp. larval stag
Page 779 and 780:
Figure 6.34 Penaeid sp. stage frequ
Page 781 and 782:
in 1981 due to the sampling pattern
Page 783 and 784:
Page 785:
5. Crangonid larvae are the least a
Page 788 and 789:
Table 7.1. Frequency of adult and j
Page 790 and 791:
7.1.2 Reproduction Reproductive sea
Page 792 and 793:
7.2.1 Larval Duration Although seve
Page 794 and 795:
7.2.2 Distribution and Abundance Si
Page 796 and 797:
Page 798 and 799:
Page 800 and 801:
into strata of the outer shelf doma
Page 802 and 803:
Figure 7.7 Vertical depth distribut
Page 804 and 805:
dark hours showed very different di
Page 807 and 808:
8.0 POSSIBLE OIL IMPACTS ON DECAPOD
Page 809 and 810:
circulating over the shelf. Current
Page 811 and 812:
Sonntag et al. (1980). Following hy
Page 813 and 814:
8.2.1 Effects on Larvae A wealth of
Page 815 and 816:
crustaceans that results in greater
Page 817 and 818:
The second hypothesized effect of o
Page 819 and 820:
proportion of infertile egg masses
Page 821 and 822:
high concentrations to be toxic. Ba
Page 823 and 824:
of oil rapidly over the surface (Le
Page 825 and 826:
strongly disagree with this hypothe
Page 827 and 828:
gal; specific gravity of oil about
Page 829 and 830:
Figure 8.2 Lease sale areas in the
Page 831 and 832:
8.4). During summer and fall, oil f
Page 833 and 834:
most of this region and, as suggest
Page 835 and 836:
found from Unimak Island to Cape Se
Page 837 and 838:
8.5.4 Other Brachyuran Larvae Larva
Page 839 and 840:
search is called for on this group
Page 841:
1. Impact of oil via water and sedi
Page 844 and 845:
Balsiger, J. W. 1976. A computer si
Page 846 and 847:
Donaldson, W. E. 1980. Alaska Tanne
Page 848 and 849:
Hameedi, M. J. 1982. The St. George
Page 850 and 851:
INPFC - International North Pacific
Page 852 and 853:
Kendall, A. W., Jr., J. R. Dunn, R.
Page 854 and 855:
Lee, R. F., C. Ryan and M. L. Neuha
Page 856 and 857:
McLaughlin, P. A. 1963. Survey of t
Page 858 and 859:
Olsen, J. C. 1961. Pandalid shrimp
Page 860 and 861:
Rathbun, M. J. 1918. The grapsoid c
Page 862 and 863:
Sitts, R., and A. Knight. 1979. Pre
Page 864 and 865:
elongatus in the northeastern and e
Page 866 and 867:
Young, A. and T. Hazlett. 1978. The
Page 869:
APPENDIX A: S.E. Bering Sea shrimp
Page 872 and 873:
APPENDIX B. References used for ide
Page 875:
Distinguishing Between Chionoecetes
Page 879 and 880:
DISTINGUISHING BETWEEN CHIONOECETES
Page 881 and 882:
Measurements were made of PLS lengt
Page 883 and 884:
Figure 1. Comparison of PLS length
Page 885 and 886:
Table 1. Rostral-dorsal lengths of
Page 887 and 888:
We also compared our diagnostic fea
show all

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