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Table 2. Clearance rates for all items naturally present in the stomachs of juvenile king crab. V = proportion of the initial value for the volume of solids as a percentage of maximum stomach volume. This average initial value of solids volume was 23.1 (± 2.4 SD) %. W = proportion of the initial value for the gram dry weight of stomach contents per gram crab wet weight. The average initial value for the dry weight was 2.91 (± 1.51) mg dry weight/g crab wet weight. T = time in hours after isolation. T = mean life, the reciprocal of the decay constant.
examined entered the dry weight analysis discussed below, <strong>and</strong> in some cases also entered the immunoassay. Thus, for larger juveniles both visual <strong>and</strong> immunological analyses were performed on the same stomachs. The smallest juvenile king crab (CL
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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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Page 138 and 139: ** SPECTRUM DISPLAY/EDIT **
Page 147 and 148: ** SPECTRUM DISPLAY/EDIT**
Page 153 and 154: ** SPECTRUM DISPLAY/EDIT **X
Page 155: APPENDIX V: SERRIPES GROENLANDICUS:
Page 165: FEEDING ECOLOGY OF JUVENILE KING AN
Page 168 and 169: DIETARY COMPOSITION ...............
Page 170 and 171: Figure 13a. Loss of precipitin reac
Page 172 and 173: Table 10. Dietary composition of ju
Page 175 and 176: ABSTRACT To determine the food requ
Page 177 and 178: FEEDING ECOLOGY OF JUVENILE KING AN
Page 179 and 180: Figure 1.--Station locations during
Page 181 and 182: Figure 3. Station locations during
Page 183 and 184: efore freezing. From large catches
Page 185 and 186: percentage of the maximum stomach v
Page 187: The amount evacuated is given by th
Page 191 and 192: Battelle's Pacific Northwest Divisi
Page 193 and 194: tows and trawling as techniques for
Page 195 and 196: Stomach fullness plotted against ti
Page 197 and 198: Figure 4. Decay curve for the clear
Page 199 and 200: life of the compartment. Similarly,
Page 201 and 202: Figure 6. Exponential decay curve f
Page 203 and 204: Figure 8. Exponential decay curve f
Page 205 and 206: A comparison of the equations in Ta
Page 207 and 208: hard parts with the palps and then
Page 209 and 210: Figure 10. Standardized dry weight
Page 211 and 212: Table 5. Diel feeding chronology fr
Page 213 and 214: These results are comparable to tho
Page 215 and 216: Figure 12. The frequency of newly d
Page 217 and 218: Table 7. Continued
Page 219 and 220: Table 9. Dietary composition (% fre
Page 221 and 222: Table 11. Dietary composition of ju
Page 223 and 224: Table 12. Dietary composition (% fr
Page 225 and 226: Table 14. Soft tissue to hard tissu
Page 227 and 228: Table 16. Dietary composition (% of
Page 229 and 230: polychaetes in both June and August
Page 231 and 232: Table 18. Continued 221
Page 233 and 234: and, therefore, had a caloric value
Page 235 and 236: Table 21. Caloric intake from vario
Page 237 and 238: Table 23. Caloric intake from vario
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Table 25. 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
Page 450 and 451:
Page 452 and 453:
Page 454 and 455:
Page 456 and 457:
Page 458 and 459:
Page 460 and 461:
Page 462 and 463:
Page 465 and 466:
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 476 and 477:
Page 478 and 479:
Page 480 and 481:
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
Page 494 and 495:
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
Page 502 and 503:
Table 4.5 Table 4.6 Table 5.1 Table
Page 505 and 506:
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
Page 518 and 519:
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
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522
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524
Page 536 and 537:
526
Page 538 and 539:
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
Page 546 and 547:
Fig. 3.4. Distribution of male red
Page 548 and 549:
Figure 3.5. Abundance estimates of
Page 550 and 551:
pheromone cues could impair males'
Page 552 and 553:
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.
Page 576 and 577:
Table 3.2. A summary of larval red
Page 578 and 579:
Fig. 3.15. Distribution and relativ
Page 580 and 581:
Fig. 3.16. Interannual differences
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[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
Page 592 and 593:
Fig. 3.21. Vertical distribution of
Page 594 and 595:
consequences of oil exposure scenar
Page 596 and 597:
abundance in time and space is corr
Page 598 and 599:
Female crabs were abundant in strat
Page 600 and 601:
observing that: 1) the mature femal
Page 602 and 603:
Much research on king crab biology
Page 604 and 605:
12) Determine interannual differenc
Page 606 and 607:
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
Page 620 and 621:
Fig. 4.4. Timing of appearance of l
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Table 4.3. Timing of appearance of
Page 624 and 625:
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
Page 630 and 631:
assumes a relatively homogeneous di
Page 632 and 633:
Methods for analysis of depth distr
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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:
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
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to as wide as 250 mm wide by a maxi
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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
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examining their vertical larval dis
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also July of 1981. Within strata, b
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Figure 5.3 Seasonal occurrence of l
Page 671 and 672:
Figure 5.5 Mean density and one sta
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Long-shelf density of Erimacrus lar
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Figure 5.6 Frequency-of-occurrence
Page 677 and 678:
Page 679 and 680:
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Figure 5.10 Distribution of mean de
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Figure 5.12 Distribution of mean de
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at 21% of all stations sampled and
Page 687 and 688:
Table 5.7. Frequency of occurrence
Page 690 and 691:
1980
Page 692 and 693:
2) In May and June of all years com
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Figure 5.15 Locations and densities
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excess of 100,000/100 m² were foun
Page 698 and 699:
Page 700 and 701:
Distribution and Abundance: Larvae
Page 702 and 703:
Table 5.10. Stratum number Frequenc
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Figure 5.20. Mean density and one s
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Pandalus borealis - Haynes 1979 Pan
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Table 6.1. Comparison of life histo
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this age are non-reproducing or ste
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Bering Sea stocks during the early
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in the Bering Sea but Butler (1980)
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6.3 Hippolytidae The Hippolytidae a
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summer food for spotted seals. Fede
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21% of the 1976 tows (Feder 1978).
Page 722 and 723:
Figure 6.1 Frequency of occurrence
Page 724 and 725:
Page 726 and 727:
A stage frequency histogram for P.
Page 728 and 729:
Figure 6.4 Pandalus tridens stage f
Page 730 and 731:
ottom. A pandalid larval type that
Page 732 and 733:
Pandalopsis dispar was taken only o
Page 734 and 735:
Page 736 and 737:
Page 738 and 739:
Figure 6.10 P. borealis larval abun
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outer shelf with the oceanic area b
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Since P. tridens occurred less freq
Page 744 and 745:
Page 746 and 747:
outer shelf during those years. Sam
Page 748 and 749:
Figure 6.16 Vertical depth distribu
Page 750 and 751:
Page 752 and 753:
SI zoeae were first taken in March
Page 754 and 755:
Page 756 and 757:
Page 758 and 759:
Table 6.7. Cross-shelf comparison o
Page 760 and 761:
during PROBES 1980 and 1981 samplin
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4) Larvae were distributed homogene
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Figure 6.25 Crangon spp. stage freq
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Figure 6.26 Argis spp. distribution
Page 768 and 769:
Page 770 and 771:
Page 772 and 773:
Figure 6.31 Crangon spp. larval abu
Page 774 and 775:
Page 776 and 777:
2) The intermolt period of about 2
Page 778 and 779:
Figure 6.33, these deepwater shrimp
Page 780 and 781:
Page 782 and 783:
Page 784 and 785:
3) Larvae were in the water column
Page 787 and 788:
7.0 DISTRIBUTION AND ABUNDANCE OF H
Page 789 and 790:
Table 7.2. Reproductive data for fo
Page 791 and 792:
and 1976 (between the Pribilof Isla
Page 793 and 794:
Figure 7.1 Paguridae stage frequenc
Page 795 and 796:
Page 797 and 798:
Page 799 and 800:
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Figure 7.6 Mean larval densities of
Page 803 and 804:
Figure 7.8 Vertical depth distribut
Page 805:
3) Larval duration in the plankton
Page 808 and 809:
and oil transport developed for the
Page 810 and 811:
Figure 8.1 Current directions and n
Page 812 and 813:
discussed by participants at the St
Page 814 and 815:
Larval Feeding: Studies with other
Page 816 and 817:
and high resultant mortality. Sonnt
Page 818 and 819:
The third reproductive effect invol
Page 820 and 821:
to and impact on, pelagic and benth
Page 822 and 823:
3. Oil was mixed to a 50-m depth in
Page 824 and 825:
synthesis as mutagenic/teratogenic
Page 826 and 827:
One or two very weak year-classes r
Page 828 and 829:
were covered by lower concentration
Page 830 and 831:
Figure 8.3 Surface oil trajectories
Page 832 and 833:
are to the west-southwest (Fig. 8.4
Page 834 and 835:
Large volumes of oil reaching shall
Page 836 and 837:
of time in the neuston layer. If th
Page 838 and 839:
in this area and so deleterious eff
Page 840 and 841:
4. Exposure of developing eggs and
Page 843 and 844:
LITERATURE CITED Adams, A. E. 1979.
Page 845 and 846:
Butler, T. H. 1971. A review of the
Page 847 and 848:
Feder, H. M. and S. C. Jewett. 1980
Page 849 and 850:
Haynes, E. B. 1980a. Larval morphol
Page 851 and 852:
Ivanov, B. G. 1964. Results in the
Page 853 and 854:
Kurata, H. 1960. Studies on the lar
Page 855 and 856:
Douglas Wolfe, ed. Fate and Effects
Page 857 and 858:
Motoh, H. 1976. The larval stages o
Page 859 and 860:
king crab Paralithodes camtschatica
Page 861 and 862:
Roncholt, L. L. 1963. Distribution
Page 863 and 864:
Somerton, D. A. and R. A. Macintosh
Page 865 and 866:
Wencker, D. L., L. S. Incze, and D.
Page 867:
APPENDICES: A: S.E. Bering Sea Shri
Page 871 and 872:
APPENDIX B. References used for ide
Page 873:
APPENDIX C. Paguridae and Lithodida
Page 877:
TABLE OF CONTENTS ABSTRACT .......
Page 880 and 881:
zoeae of these two species from the
Page 882 and 883:
the curved lateral processes reach
Page 884 and 885:
Additional Morphological Features U
Page 886 and 887:
APPLICATION OF FINDINGS TO FIELD ST
Page 888:
Kurata, H. 1963. Larvae of Decapoda
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