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Estimating an appropriate residence time for shell fragments appears problematic but a reasonable estimate is possible. Carter and Steele (1982) found that shell fragments remained in lobster stomachs 90 to 180 d (2160 to 4320 h). Hill (1976) observed no decrease in the weight of shell fragments in the stomachs of the crab, Scylla serrata, during 8 days of observations while soft tissue fell to 5% of its initial level in 12 h and fishbone, to less than 5% in about 3.5 days (about 84 h). Here barnacle tissue reached 5% of its initial dry weight at 3.0 x 10[superscript]4 h, i.e., 1250 days. Hard tissue, such as barnacle plates and molluscan shell fragments, appear to remain indefinitely in crab stomachs. Hill suggests that crabs regurgitate shell rather than evacuate it into the lower digestive system. Pearson and Olla (1977) and Pearson et al (1979) have seen captive blue crab, Callinectes sapidus, and Dungeness crab, Cancer magister, periodically regurgitate shell when held on an ad libitum diet of blue mussels. During shipboard holding of juvenile king crab regurgitation of shell and sand dollar test fragments was observed. These observations suggest that shell fragments and other hard tissue remain indefinitely in crab stomachs accumulating to some threshold volume at which point the crab regurgitates the entire volume. If so, the problem becomes one of determining the time frame within which the regurgitation will normally occur. On shipboard juvenile king crabs held without food regurgitated shell beginning 4 days after capture and continuing each night until the crabs were used in an experiment at 12 days after isolation. Five crabs sacrificed 7 days after isolation had no visible shell fragments in their guts, but dry weights of stomach contents for these individuals were not determined. Both Hill's (1976) data and that presented here indicate shell fragments have a longer stomach residence time than fish bone. In light of the available information, a stomach residence time for hard tissue such as shell fragments appears to be more than 5.4 days and could be on the order of 135 days for crustaceans continuing to feed on soft tissue. The shipboard observations on regurgitation and visual examination of the stomachs would indicate a residence time between 4 and 7 days. The exponential model would indicate one of 1250 days. The harmonic mean of these four estimates is 10.7 days. This latter value was used in corrections for gut residence times. SHIPBOARD OBSERVATIONS OF FEEDING BEHAVIOR On shipboard, juvenile king crabs selectively ingested only certain parts of some prey. Crabs ate the fleshy portions of the shrimp and juvenile fish, leaving the heads. Similarly, crabs ingested little of the barnacle plates and mussel shell. Crabs scraped the soft tissue from the 196
hard parts with the palps and then dropped the cleaned hard parts. Only small fragments of plate or shell were ingested. Previously Pearson et al (1979,1981) have seen similar selective feeding on soft tissue and discarding of hard parts by the Dungeness crab, C. magister. The implication of the selective ingestion observed in the juvnenile king crab is that in actively selecting soft tissue and rejecting hard tissue, the crab is not ingesting prey items in proportion to the occurrence of hard parts of those items in the stomach. For example, juvenile king crab could well be consuming more clams than the presence of shell fragments indicates. DIEL FEEDING CHRONOLOGY Diel feeding chronologies were determined for June and August (Figures 9, 10 and 11). In June juvenile king crab were not sampled at every hour of the day, but in August 25 crabs were obtained in each 2-h period of the 24-h cycle. In October only one juvenile king crab greater than 20 mm CL was collected. Consequently, the best estimate of the diel feeding chronology for juvenile king crab came from August. For tanner crab the sample sizes for crabs greater than 20 mm CW were inadequate to construct a diel feeding chronology. Tanner crab less than 20mm CW had extremely small stomach volumes (
Page 1 and 2:
Outer Continental Shelf Environment
Page 5:
OUTER CONTINENTAL SHELF ENVIRONMENT
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Outer Continental Shelf Environment
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TABLE OF CONTENTS List of Figures 5
Page 15 and 16:
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
Page 54 and 55:
Page 56 and 57:
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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
Page 113:
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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Page 127 and 128:
XX SPECTRUM DISPLAV/EDIT **
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Page 131 and 132:
** SPECTRUM DISPLAVY/EDIT **
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APPENDIX III: ASTARTE BOREALIS: BAY
Page 136 and 137:
Page 138 and 139:
Page 140 and 141:
Page 142 and 143:
Page 145 and 146:
Page 147 and 148:
** SPECTRUM DISPLAY/EDIT**
Page 149 and 150:
Page 151 and 152:
Page 153 and 154:
** SPECTRUM DISPLAY/EDIT **X
Page 155: APPENDIX V: SERRIPES GROENLANDICUS:
Page 158 and 159: ** SPECTRUM DISPLAY/EDIT **
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 and 188: The amount evacuated is given by th
Page 189 and 190: examined entered the dry weight ana
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: A comparison of the equations in Ta
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 241 and 242: Table 27. Results of visual examina
Page 243 and 244: They were then fed thawed juvenile
Page 245 and 246: eing tested rather than to cross re
Page 247 and 248: against its respective antigen and
Page 249 and 250: Table 29. Results of visual examina
Page 251 and 252: DISCUSSION IMMUNOASSAY The immunolo
Page 253 and 254: juvenile king crabs may depend on c
Page 255 and 256: Table 32. Comparison of August diet
Page 257 and 258:
stomach contents but soft-bodied po
Page 259 and 260:
The assumption that, at least for t
Page 261 and 262:
shows high similiarity between the
Page 263 and 264:
supply requires prediction of the s
Page 265 and 266:
have been shown to readily and rapi
Page 267 and 268:
Using the diel feeding chronologies
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to 70 m, potential effects from dis
Page 271 and 272:
REFERENCES Addy, J. M., D. Levell,
Page 273 and 274:
Hill, B. J. 1976. Natural food, for
Page 275:
Tyler, A. V, 1973. Caloric values o
Page 279:
CLARIFICATION All references to "se
Page 282 and 283:
4.0 DISCUSSION ....................
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Figure 3.2-2 Cruise 83-3 larval red
Page 287 and 288:
ACKNOWLEDGEMENTS This study was ori
Page 289 and 290:
ABSTRACT The goal of this study was
Page 291 and 292:
SECTION 1.0 INTRODUCTION The red ki
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1.1 Study Objectives The goal of th
Page 295 and 296:
than 50 m. The oceanography of the
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entering the fishery have declined
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females. This relationship supports
Page 301 and 302:
time to temperature. Time from egg-
Page 303:
Juvenile crab in 2+ to 3+ age class
Page 306 and 307:
BRISTOL BAY RED KING CRAB CRUISE 83
Page 308 and 309:
Page 310 and 311:
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
Page 318 and 319:
200 individuals of the most common
Page 320 and 321:
BRISTOL BAY RED KING CRAB STUDY ARE
Page 322 and 323:
Epibenthic density and biomass data
Page 324 and 325:
Page 326 and 327:
Page 328 and 329:
Page 330 and 331:
Page 332 and 333:
Page 334 and 335:
Page 336 and 337:
little vertical temperature stratif
Page 338 and 339:
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
Page 344 and 345:
BRISTOL BAY RED KING CRAB SIDE-SCAN
Page 346 and 347:
Page 348 and 349:
TABLE 3.2-1 MEAN LARVAL RED KING CR
Page 350 and 351:
stations in this area where larval
Page 352 and 353:
three-day period in June showed rat
Page 354 and 355:
BRISTOL BAY RED KING CRAB DIEL VERT
Page 356 and 357:
TABLE 3.3-1 GEOMETRIC MEAN DENSITIE
Page 358 and 359:
during the June cruise (83-3). duri
Page 360 and 361:
TABLE 3.4-2 NUMBER OF POST LARVAL R
Page 362 and 363:
TABLE 3.4-3 NUMBER OF POST LARVAL R
Page 364 and 365:
BRISTOL BAY RED KING CRAB TRYNET SA
Page 366 and 367:
BRISTOL BAY RED KING CRAB TRYNET AN
Page 368 and 369:
BRISTOL BAY RED KING CRAB DISTRIBUT
Page 370 and 371:
Page 372 and 373:
NORTH ALEUTIAN BASIN RED KING CRAB
Page 374 and 375:
TABLE 3.5-3 CORRELATION MATRIX FOR
Page 376 and 377:
TABLE 3.5-5 CORRELATION MATRIX FOR
Page 378 and 379:
Page 380 and 381:
Page 382 and 383:
at one 50 m deep TB station west of
Page 384 and 385:
TABLE 3.6-2 SUMMARY OF BIOLOGICAL I
Page 386 and 387:
TABLE 3.7-1 SUMMARY OF TRYNET CATCH
Page 388 and 389:
Page 390 and 391:
group AB, especially the fish speci
Page 392 and 393:
BRISTOL BAY RED KING CRAB LARVAL DE
Page 394 and 395:
BRISTOL BAY RED KING CRAB LARVAL DE
Page 396 and 397:
BRISTOL BAY RED KING CRAB KNOWN CIR
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Bay and west to Cape Newenham. The
Page 400 and 401:
BRISTOL BAY RED KING CRAB 1978, 197
Page 402 and 403:
protection against predators, as we
Page 404 and 405:
which provides for adequate food (i
Page 406 and 407:
4.5 Potential Effects of Oil and Ga
Page 408 and 409:
to a great extent tidally driven, t
Page 410 and 411:
(1983b), the same volume of oil is
Page 412 and 413:
BRISTOL BAY RED KING CRAB SURFACE O
Page 414 and 415:
Overt, rapid mortality of adult cra
Page 416 and 417:
viability of the gametes is impaire
Page 418 and 419:
detected by chemosensory organs. Pe
Page 420 and 421:
and Alaskan species of shrimp and c
Page 422 and 423:
interannual variability in abundanc
Page 424 and 425:
that are killed by oil north of Uni
Page 426 and 427:
Long-term, sublethal effects may al
Page 428 and 429:
Botsford, L. and D. Wickham. 1978.
Page 430 and 431:
Harris, R.P., V. Bergudugo, E.D.S.
Page 432 and 433:
Kurata, H. 1961. Studies on the lar
Page 434 and 435:
Paul, A.J., J. Paul, P. Shoemaker a
Page 436 and 437:
Takeuchi, I. 1962, trans. 1967. On
Page 439:
APPENDIX A MEAN LARVAL RED KING CRA
Page 443 and 444:
APPENDIX B TRAWL GEAR TYPES USED BY
Page 445:
APPENDIX C: TRAWL/DREDGE NOTES 435
Page 448 and 449:
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
Page 467 and 468:
APPENDIX D (continued) 457
Page 469:
APPENDIX E: MULTIPLE LINEAR REGRESS
Page 472 and 473:
APPENDIX E (continued) 462
Page 474 and 475:
Page 476 and 477:
Page 478 and 479:
Page 480 and 481:
Page 483:
APPENDIX F: JUVENILE RED KING CRAB
Page 486 and 487:
APPENDIX F (continued) Figure Fl. S
Page 489:
DISTRIBUTION AND ABUNDANCE OF DECAP
Page 492 and 493:
4.0 DISTRIBUTION AND ABUNDANCE OF T
Page 494 and 495:
8.3 Larval Decapod Biology, Sensiti
Page 496 and 497:
Figure 3.4 Figure 3.5 Figure 3.6 Fi
Page 498 and 499:
Figure 5.8 Distribution and abundan
Page 500 and 501:
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
Page 507 and 508:
1.0 GENERAL INTRODUCTION 1.1 Justif
Page 509 and 510:
Larval stages are generally conside
Page 511 and 512:
extent in 1982) did we have the opp
Page 513:
The sections of this report describ
Page 516 and 517:
Table 2.1. Dates and sources of zoo
Page 518 and 519:
techniques which attempt to equally
Page 520 and 521:
verification of results or examinat
Page 522 and 523:
cation of these larvae and the vari
Page 524 and 525:
meters) was often similar (generall
Page 526 and 527:
Bongo frame, the MOCNESS frame cann
Page 528 and 529:
abundance within strata were made b
Page 530 and 531:
520
Page 532 and 533:
522
Page 534 and 535:
524
Page 536 and 537:
526
Page 538 and 539:
528
Page 540 and 541:
Figure 2.21 Locations and boundarie
Page 542 and 543:
Figure 3.1. Location of proposed le
Page 544 and 545:
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
Page 568 and 569:
11 and 12 (Figs. 3.11, 3.12). Too f
Page 570 and 571:
Table 3.1. Number of zooplankton sa
Page 572 and 573:
Because of the poor spatial coverag
Page 574 and 575:
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
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
Page 590 and 591:
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
Page 610 and 611:
(NMFS) since the early 1970's. In a
Page 612 and 613:
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
Page 622 and 623:
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
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:
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:
Page 679 and 680:
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 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
Page 694 and 695:
Figure 5.15 Locations and densities
Page 696 and 697:
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
Page 704 and 705:
Figure 5.20. Mean density and one s
Page 706 and 707:
Pandalus borealis - Haynes 1979 Pan
Page 708 and 709:
Table 6.1. Comparison of life histo
Page 710 and 711:
this age are non-reproducing or ste
Page 712 and 713:
Bering Sea stocks during the early
Page 714 and 715:
in the Bering Sea but Butler (1980)
Page 716 and 717:
6.3 Hippolytidae The Hippolytidae a
Page 718 and 719:
summer food for spotted seals. Fede
Page 720 and 721:
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
Page 740 and 741:
outer shelf with the oceanic area b
Page 742 and 743:
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
Page 762 and 763:
4) Larvae were distributed homogene
Page 764 and 765:
Figure 6.25 Crangon spp. stage freq
Page 766 and 767:
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:
Page 801 and 802:
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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