11th ICRS Abstract book - Nova Southeastern University

More documents

Recommendations

Info

Poster Mini-Symposium 10: Ecological Processes on Today's Reef Ecosystems 10.261 Influence Of palythoa Caribaeorum (Anthozoa, Cnidaria) Patches On Reef Fish Community in Subtropical Rocky Shores José P. MENDONÇA-NETO 1 , Laís C. T. CHAVES* 2 , Carlos E. L. FERREIRA 3 , Cassiano MONTEIRO-NETO 1 , Renato C. PEREIRA 1 1 Departamento de Biologia Marinha, Universidade Federal Fluminense, Niteroi, Brazil, 2 Departamento de Oceanografia, Universidade Federal de Pernambuco, Recife, Brazil, 3 Departamento de Biologia Marinha, Universidade Federal Fluminense, Niterói, Brazil This work aimed to test the influence of the Palythoa caribeorum, a Zoanthid widely distributed in the Atlantic, on the fish community of Arraial do Cabo rocky reefs, Southeastern Brazil. Abundance, diversity and vertical distribution of reef fish inside (ID) and outside (OD) previously chosen P. caribaeorum dominance patches were compared among two different sites. Replicated visual stationary censuses were conducted through different bathymetric zones: shallow (~0-3m); intermediate (~3-6m) and bottom (~6-9m). Sites were revisited during one year period effort (SEP06/ OCT07). A total of 180 censuses were conducted; 30 censuses on each bathymetric reef zone. Percentage cover of P. caribaeorum and other benthic organisms were obtained analyzing random points from replicated photo-quadrats (n = 30). This work resulted in 45 species belonging to 25 families. The ten most abundant fishes for both sites comprised together 65% of all fishes recorded during this study. Despite sites presented similar components on reef fish community, they differed in abundance (ANOVA, p=0.003) and richness (ANOVA, p=***), where OD patches presented higher values. We also recognized two major benthic communities occupying the same depth zones: the algal community, in which turf algae was dominant and the zoanthid community, which was dominated by P. caribaeorum. In overall view, differences between fish community among patches could be attributed to particular species for swimming ability and ontogeny. Results seem not to indicate direct effects of P. caribaeorum on reef fish community, despite some evidence that these areas might play a important role in space limitation by structuring neighboring benthic community and consequently, fish community. 10.262 Reproductive fitness consequences of parrotfish predation on a tropical reefbuilding coral: small damage, large consequence Randi ROTJAN* 1 , Sara LEWIS 2 1 Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, 2 Department of Biology, Tufts University, Medford, MA The trophic role of Caribbean parrotfish on coral reefs is controversial: while parrotfish are classically known for their role as important reef herbivores, they are also significant corallivores that selectively graze species of important reef-building corals in the Montastraea annularis species complex. While the benefits of parrotfish herbivory for coral reef resilience and conservation have been extensively documented, the consequences of parrotfish grazing for coral reproductive fitness have not been previously examined. We examined colonies of Montastraea annularis corals that had been recently grazed (within 2 weeks of sampling) by parrotfishes in order to examine whether grazing was positively associated with coral reproductive effort. We measured gonad number, egg number and size, and proportional reproductive allocation for grazed and intact Montastraea annularis colonies 2-5 days prior to their annual spawning time. We found that parrotfish selectively grazed coral tissue areas with high total reproductive effort (number of gonads), providing the first evidence that parrotfish selectively target specific tissue areas within a single coral colony. Our data suggest that the removal of polyps with high reproductive effort has direct adverse affects for coral colony fitness, with additional indirect implications for colony growth and survival. However, nearby M. annularis colonies showing high reproductive effort were not grazed by parrotfishes, suggesting that some colonies are defended against grazing. We conclude that chronic grazing by parrotfishes has negative fitness consequences for these reef-building corals, and that these previously underappreciated impacts have the potential to adversely affect reef ecosystems. 10.263 Evolutionary Ecology Of Sponge-Cyanobacteria Symbioses Robert THACKER* 1 , Patrick ERWIN 2 1 Department of Biology, University of Alabama at Birmingham, Birmingham, AL, 2 Center for Marine Science, University of North Carolina at Wilmington, Wilmington, NC Symbioses between sponges and cyanobacteria are common on coral reefs, with cyanobacterial symbionts including filamentous Oscillatoria spongeliae and unicellular Synechococcus spongiarum. We investigated the filamentous symbionts associated with two recently described species from Caribbean Panama, Haliclona walentinae and Xestospongia bocatorensis, and the unicellular symbionts associated with Aplysina fulva and Neopetrosia subtriangularis. We shaded A. fulva and N. subtriangularis to examine the effects of reduced light availability on symbiont load and host growth. We estimated the photosynthetic capacities of cyanobacterial symbionts of all four host sponges by measuring changes in dissolved oxygen concentrations in light and dark conditions. We also amplified and sequenced cyanobacterial 16S ribosomal RNA genes from each host. Six weeks of shading reduced symbiont load in A. fulva and N. subtriangularis by over 40%. In A. fulva, control sponges exhibited twice the growth of shaded sponges. In N. subtriangularis, no significant difference in growth was observed between control and shaded sponges. We observed no significant differences in respiration among the sponges tested; however, Haliclona walentinae and Xestospongia bocatorensis exhibited higher oxygen production than A. fulva and N. subtriangularis. A phylogeny of cyanobacterial 16S ribosomal RNA genes recovered from each sponge species confirmed that the symbionts of Haliclona walentinae and Xestospongia bocatorensis are part of the O. spongeliae clade and that each sponge hosts a unique ribotype of this vertically transmitted symbiont. The cyanobacteria hosted by A. fulva and N. subtriangularis are part of the S. spongiarum clade, which shows less host specificity despite evidence of vertical transmission. Ecological interactions between sponges and their cyanobacterial symbionts vary among host species, spaning a range of interactions from commensalisms to facultative and obligate mutualisms. 10.264 Growth strategy of a dominant reef-building coral in the southern Caribbean: Agaricia tenuifolia Silvia CACERES* 1 , Juan Armando SANCHEZ 2 1 2 Biologia, universidad de los Andes, Bogota, Colombia, Biologia, Universidad de los Andes, Bogota, Colombia Shifts have occurred in the coral community structure at Caribbean reefs, particularly regarding dominance, which are not yet understood completely. The branching scleractinian coral, Agaricia tenuifolia (thin leaf lettuce coral), is the dominant coral species in shallow reefs at many Southern and Western Caribbean reefs. To estimate the population fluctuation and growth strategy colonies of A. tenuifolia in the Southern Caribbean (Cartagena, Colombia) were followed over a year and a half using photograph censuses and in situ growth measurements. A size class model was generated in order to estimate colonial growth rate and clonal processes (e.g., fission and fusion events). Overall population abundance was stable over the monitored period, but differed between locations. The largest size class was directly responsible to the dominant abundance of A. tenuifolia. Mortality patterns were not correlated to colonial size classes and were variable in space and time. Fusion was also an important process in A. tenuifolia but not as common as fission. Colonial growth rate was correlated to the colony size class, the interaction between the location and the size class, the aggregation of multiple colonies and possibly multiple genets. Clonal strategies, as bet hedges, allowed species like A. tenuifolia to avoid the vulnerability to survive and compete that is often associated with early post-settlement larvae. The A. tenuifolia population showed a dynamic life pattern with variable rates for clonal processes that play an important descriptive role of the population together with the size distribution frequency. A. tenuifolia is normally extracted as a souvenir in the Southern Caribbean. Quantifying the changes in the population structure and size frequency is important to manage this resource as it is necessary to perform long-term observations and coral extraction experiments. 329
Poster Mini-Symposium 10: Ecological Processes on Today's Reef Ecosystems 10.265 Zoantharia Habitat Preference Depending On Host Sponge Morphology Alberto ACOSTA* 1 , Javier MONTENEGRO* 2 1 Biology, Pontificia Universidad Javeriana, Bogota, Colombia, 2 Pontificia Universidad Javeriana, Bogota, Colombia Population’s habitat preference is hard to estimate for some species due to their complex life histories, spatial and temporal variation in resource selection criteria by organisms, and difficulty in habitat delimitation. Some symbiotic genera of zoantharian (Hexacorallia) can serve as optimal models to evaluate habitat preference, not only because their habitat (host sponge) could be easily delimited, but also because the habitat selected by larvae will have an effect in the fitness of the adult colony. According to this, we studied the Parazoanthus and Epizoanthus genera in order to demonstrate whether their habitat preference is related to sponge (host) morphology. The presence/absence of zoanthids in a total of 1,068 sponges was recorded in San Andres Island (Caribbean). The sponge shape was categorized as: cup, tubular, encrusting, globular and branching, and the mechanic resistance (MR) as: compressible, elastic, and fragile. Habitat preference was evaluated using the most important indices and Bonferroni confidence intervals. 109 zoantharian colonies were associated to sponges (10.2%) of which 85 and 24 were Parazoanthus (8.0%) and Epizoanthus (2.2%) respectively. The colony frequency of both genera was significantly dependent of the sponge shape and MR (p
Page 2 and 3:
Contents Sponsors..................
Page 4 and 5:
Sponsors 11th ICRS Co-Sponsors Barr
Page 6 and 7:
Mini-Symposium Co-Chairs Mini-Sympo
Page 8:
Mini-Symposium 23: Reef Management
Page 12 and 13:
Plenary Lessons from the Past Malco
Page 14:
Plenary Drivers of Coral Infectious
Page 18 and 19:
1-1 The R/v Alpha Helix Symbios Exp
Page 20 and 21:
1-9 Coral Community Change Over A C
Page 22 and 23:
1-17 Holocene Reef Development At T
Page 24 and 25:
1-25 Paleoecology Of Mio-Pliocene F
Page 26 and 27:
Oral Mini-Symposium 2: Biotic Respo
Page 28 and 29:
Oral Mini-Symposium 2: Biotic Respo
Page 30 and 31:
Oral Mini-Symposium 3: Calcificatio
Page 32 and 33:
Oral Mini-Symposium 3: Calcificatio
Page 34 and 35:
3-17 The Effect Of Depressed Aragon
Page 36 and 37:
Oral Mini-Symposium 4: Coral Reef O
Page 38 and 39:
Page 40 and 41:
Page 42 and 43:
Page 44 and 45:
Oral Mini-Symposium 5: Functional B
Page 46 and 47:
Page 48 and 49:
Page 50 and 51:
Page 52 and 53:
Page 54 and 55:
Page 56 and 57:
Oral Mini-Symposium 6: Ecological a
Page 58 and 59:
Page 60 and 61:
Page 62 and 63:
Page 64 and 65:
7-5 Coral Yellow Band Disease; Curr
Page 66 and 67:
7-13 Black Band Disease (BBD): A Po
Page 68 and 69:
7-21 Coral Host Processes Associate
Page 70 and 71:
7-29 Can the Presence of Disease Si
Page 72 and 73:
7-37 Developing An Expert System Fo
Page 74 and 75:
7-45 The Effect Of Sediment And Hea
Page 76 and 77:
8-1 From Bacterial Bleaching To The
Page 78 and 79:
8-9 Milkfish Feces Share Common Bac
Page 80 and 81:
8-17 Bacteria Associated With Symbi
Page 82 and 83:
8-26 Photosynthetic Microorganisms
Page 84 and 85:
8-35 Tissue Loss And Tropical Storm
Page 86 and 87:
9-5 Evaluation Of Biotic And Abioti
Page 88 and 89:
9-13 Is Allelopathy Involved in Cor
Page 90 and 91:
Oral Mini-Symposium 10: Ecological
Page 92 and 93:
Page 94 and 95:
Page 96 and 97:
Page 98 and 99:
Page 100 and 101:
10-41 Substrate Effects On Reef Fis
Page 102 and 103:
Page 104 and 105:
Page 106 and 107:
Page 108 and 109:
Oral Mini-Symposium 11: From Molecu
Page 110 and 111:
Page 112 and 113:
Page 114 and 115:
Page 116 and 117:
Page 118 and 119:
12-5 The Contribution Of Heterotrop
Page 120 and 121:
12-14 Ocean Dynamics Drive Coral Re
Page 122 and 123:
12-23 Coral Reef Resilience To Chro
Page 124 and 125:
13-1 Prioritizing Conservation Hots
Page 126 and 127:
Oral Mini-Symposium 13: Evolution a
Page 128 and 129:
14-6 Modelling Coral Larval Dispers
Page 130 and 131:
14-14 Environmentally-Mediated Vari
Page 132 and 133:
14-21 Same, Same, But Different: Co
Page 134 and 135:
14-29 Complex Patterns of Genetic C
Page 136 and 137:
14-37 Genetic Connectivity in Phili
Page 138 and 139:
14-45 Range-Wide Population Genetic
Page 140 and 141:
14-55 The Importance Of Behavior On
Page 142 and 143:
Oral Mini-Symposium 15: Progress in
Page 144 and 145:
Oral Mini-Symposium 15: Progress in
Page 146 and 147:
Oral Mini-Symposium 16: Ecosystem A
Page 148 and 149:
Page 150 and 151:
Page 152 and 153:
Page 154 and 155:
Page 156 and 157:
Page 158 and 159:
Oral Mini-Symposium 17: Emerging Te
Page 160 and 161:
Page 162 and 163:
Page 164 and 165:
Page 166 and 167:
Page 168 and 169:
18-5 Coral Reef Habitat Around New
Page 170 and 171:
18-13 Response Of High Latitude Her
Page 172 and 173:
18-21 Socio-Economic Monitoring (So
Page 174 and 175:
18-29 Extent And Timing Of Disturba
Page 176 and 177:
18-37 It Depends On Where You Look:
Page 178 and 179:
18-45 New Insights Into The Exposur
Page 180 and 181:
Oral Mini-Symposium 19: Biogeochemi
Page 182 and 183:
Page 184 and 185:
Page 186 and 187:
Page 188 and 189:
Oral Mini-Symposium 20: Modeling Co
Page 190 and 191:
Oral Mini-Symposium 20: Modeling Co
Page 192 and 193:
21-9 Integrated Economic Valuation
Page 194 and 195:
21-19 Towards Local Fishers Partici
Page 196 and 197:
21-27 The Political Aspects Of Resi
Page 198 and 199:
21-37 Exploitation And Trade Of Cor
Page 200 and 201:
22-1 Complex Ecological Effects Of
Page 202 and 203:
22-9 Comparative Evaluation Of Reef
Page 204 and 205:
22-17 Managing Fishing Gear To Enco
Page 206 and 207:
22-25 Estimating Harvest Pressure O
Page 208 and 209:
22-33 Are The Coral Reef Finfish Fi
Page 210 and 211:
22-41 Using Length-Frequency Data T
Page 212 and 213:
22-50 Changes in Ecosystem Structur
Page 214 and 215:
23-5 Measuring Success in Managing
Page 216 and 217:
23-13 Some Hints About The Impacts
Page 218 and 219:
23-21 Fishery Management For Artisa
Page 220 and 221:
23-29 “To Live With The Sea”; D
Page 222 and 223:
23-37 Challenges Facing An Mpa Mana
Page 224 and 225:
23-45 Assessing Global Coral Reef M
Page 226 and 227:
23-53 Developing A Model For Ecosys
Page 228 and 229:
23-61 Mitigating The Effects Of Cor
Page 230 and 231:
23-69 Restore Or Not To Restore? Vl
Page 232 and 233:
24-1 Fates Of Restored Acropora Pal
Page 234 and 235:
24-9 Sponge-Mediated Coral Reef Res
Page 236 and 237:
24-17 Coral Community Restorations
Page 238 and 239:
24-25 Development Of A Coral Nurser
Page 240 and 241:
24-33 Transplantation of Porites lu
Page 242 and 243:
24-41 Scleractinian Coral Relocatio
Page 244 and 245:
24-50 Gametogenesis in Cultured Ver
Page 246 and 247:
Oral Mini-Symposium 25: Predicting
Page 248 and 249:
Page 250 and 251:
Page 252 and 253:
Page 254 and 255:
Page 256 and 257:
Page 258 and 259:
Page 260 and 261:
Oral Mini-Symposium 26: Biodiversit
Page 262 and 263:
Page 264 and 265:
Page 266 and 267:
Page 268 and 269:
Page 270 and 271:
Page 272 and 273:
26-54 Gene Genealogies Reveal Phylo
Page 274 and 275:
Page 276:
Poster Session
Page 279 and 280:
1.13 Depth-Related Patterns of Infa
Page 281 and 282:
1.20 Grain Size And Sedimentary Con
Page 283 and 284:
1.3 Environmental Effects On Back-R
Page 285 and 286:
Poster Mini-Symposium 2: Biotic Res
Page 287 and 288:
Poster Mini-Symposium 3: Calcificat
Page 289 and 290:
Page 291 and 292:
Page 293 and 294:
Poster Mini-Symposium 4: Coral Reef
Page 295 and 296: Poster Mini-Symposium 4: Coral Reef
Page 301 and 302: Poster Mini-Symposium 5: Functional
Page 319 and 320: Poster Mini-Symposium 6: Ecological
Page 321 and 322: 7.162 Disease Ecology And Local Pat
Page 323 and 324: 7.170 Coralline Algal Disease in Th
Page 325 and 326: 7.179 Physiological Effects Of Aspe
Page 327 and 328: 7.187 Characterizing Surface Microo
Page 329 and 330: 7.195 How Quickly Does gorgonia Ven
Page 331 and 332: 7.203 Spatial and temporal variabil
Page 333 and 334: 8.210 Quorum Sensing Inhibitory Act
Page 335 and 336: 8.218 Bacterial Communities Associa
Page 337 and 338: 8.226 Bacterial Growth On Coral Muc
Page 339 and 340: 8.234 Functional Diversity of Micro
Page 341 and 342: 8.242 Microbial Community Profile O
Page 343 and 344: 9.248 Chemistry And Ecology Of A Co
Page 345: Poster Mini-Symposium 10: Ecologica
Page 349 and 350: Poster Mini-Symposium 10: Ecologica
Page 377 and 378: Poster Mini-Symposium 11: From Mole
Page 383 and 384: 12.413 Spatial Patterns Of Stony Co
Page 385 and 386: Poster Mini-Symposium 13: Evolution
Page 387 and 388: Poster Mini-Symposium 13: Evolution
Page 389 and 390: 14.432 Gene flow of Symbiodinium on
Page 391 and 392: 14.441 Population Genetics Of Spott
Page 393 and 394: 14.449 Mitochondrial Phylogeography
Page 395 and 396: 14.457 Undirect Evidences On The Co
Page 397 and 398:
14.466 South East African, High-Lat
Page 399 and 400:
14.474 Population Genetic Structure
Page 401 and 402:
14.483 Influences Of Wind-Wave Expo
Page 403 and 404:
14.491 Distributions And Diversity
Page 405 and 406:
14.499 Do Mangroves And Seagrass Be
Page 407 and 408:
14.507 Genetic variation of the hyd
Page 409 and 410:
Poster Mini-Symposium 15: Progress
Page 411 and 412:
Poster Mini-Symposium 15: Progress
Page 413 and 414:
Poster Mini-Symposium 16: Ecosystem
Page 415 and 416:
Page 417 and 418:
Page 419 and 420:
Poster Mini-Symposium 17: Emerging
Page 421 and 422:
Page 423 and 424:
Page 425 and 426:
Page 427 and 428:
Page 429 and 430:
Page 431 and 432:
18.599 A Palaeoecological Perspecti
Page 433 and 434:
18.607 Susceptibility Of Corals To
Page 435 and 436:
18.616 Coral Reefs in Costa Rican C
Page 437 and 438:
18.624 Environmental Endocrine Disr
Page 439 and 440:
18.633 Northern Acehnese Coral Reef
Page 441 and 442:
18.641 The Status Of Coral Reefs in
Page 443 and 444:
18.649 The Effects of Increased Sea
Page 445 and 446:
18.658 “Changing Times, Changing
Page 447 and 448:
18.666 Assessing Land Based Inputs
Page 449 and 450:
18.674 Monitoring Of Coral Recovery
Page 451 and 452:
18.682 Seasonal Investigation On St
Page 453 and 454:
18.690 Assessment Of The Coral Reef
Page 455 and 456:
18.698 Distribution Of Seagrasses i
Page 457 and 458:
18.706 Coral Reef Monitoring in the
Page 459 and 460:
18.714 Pacific-Wide Status Of The R
Page 461 and 462:
18.722 Quantitative Underwater Ecol
Page 463 and 464:
18.730 Community Structure Of Reef
Page 465 and 466:
18.738 Morphological Variation In T
Page 467 and 468:
18.746 Decade-Long (1998-2007) Tren
Page 469 and 470:
18.755 Coral Community Composition
Page 471 and 472:
18.763 Changes in Coral Reef Ecosys
Page 473 and 474:
18.771 Bathymetric Distribution Of
Page 475 and 476:
Poster Mini-Symposium 19: Biogeoche
Page 477 and 478:
Page 479 and 480:
Page 481 and 482:
Poster Mini-Symposium 20: Modeling
Page 483 and 484:
21.807 The Recreational Value Of Co
Page 485 and 486:
21.815 Dilemma in Coral Conservatio
Page 487 and 488:
22.821 Estimating Populations Of Tw
Page 489 and 490:
22.829 Commercial Topshell, trochus
Page 491 and 492:
22.837 Trajectories Of Ecosystem Ch
Page 493 and 494:
22.845 Ornamental Fish Trade in The
Page 495 and 496:
22.854 Short-Term Recovery Of Explo
Page 497 and 498:
22.863 Marine Protected Areas: Boon
Page 499 and 500:
22.871 Rotary Time-Lapse Photograph
Page 501 and 502:
22.879 Assessing And Mapping The Di
Page 503 and 504:
22.887 Spatial Variations in Elemen
Page 505 and 506:
23.1004 Coral Reef Conservation Cam
Page 507 and 508:
23.1014 Second And Third Order Mana
Page 509 and 510:
23.1023 Why do Divers Dive Where Th
Page 511 and 512:
23.1031 The Colonial Tunicate tridi
Page 513 and 514:
23.1039 Effectiveness Of A Small Mp
Page 515 and 516:
23.893 Man Made Stress Reliever? An
Page 517 and 518:
23.901 Reef Monitoring Project For
Page 519 and 520:
23.909 Patterns Of Spatial Variabil
Page 521 and 522:
23.917 Culture And Updated Traditio
Page 523 and 524:
23.925 Scientific Monitoring And Cu
Page 525 and 526:
23.934 Characterizing Local Stakeho
Page 527 and 528:
23.942 Challenges in Coral Reef Man
Page 529 and 530:
23.951 Coral Reef-Based Tourism And
Page 531 and 532:
23.959 Marine Protected Area Report
Page 533 and 534:
23.967 Reef Watch Monitoring And Ho
Page 535 and 536:
23.975 A Comparison Of The Permanen
Page 537 and 538:
23.984 Damselfish Embryo Assay: Fie
Page 539 and 540:
23.992 The Decline Of Coral Reef Co
Page 541 and 542:
24.1043 Characteristics Of Seagrass
Page 543 and 544:
24.1051 Mass Culture Of acropora Co
Page 545 and 546:
24.1059 Identifying Sediment-Tolera
Page 547 and 548:
24.1067 Growth Of Newly Settled Ree
Page 549 and 550:
24.1076 Herbivore Effects On Coral
Page 551 and 552:
24.1084 Coral Reefs Conservation Pr
Page 553 and 554:
24.1092 Lessons Learned On Demonstr
Page 555 and 556:
24.1100 Proceedings in Shipgroundin
Page 557 and 558:
24.1108 Restoring An Artificial "En
Page 559 and 560:
24.1116 A Newly Established Coral R
Page 561 and 562:
24.1124 Is The Scale Of Your Coral
Page 563 and 564:
Poster Mini-Symposium 25: Predictin
Page 565 and 566:
Page 567 and 568:
Page 569 and 570:
Page 571 and 572:
Page 573 and 574:
Poster Mini-Symposium 26: Biodivers
Page 575 and 576:
Page 577 and 578:
Page 579 and 580:
Page 581 and 582:
Page 583 and 584:
Page 585 and 586:
Page 587 and 588:
Page 589 and 590:
Page 591 and 592:
Memo ..............................
Page 593 and 594:
Authors INDEX Author Session Page A
Page 595 and 596:
Page 597 and 598:
Page 599 and 600:
Page 601 and 602:
Page 603 and 604:
Page 605 and 606:
Page 607 and 608:
Page 609 and 610:
Page 611 and 612:
Page 613 and 614:
Page 615 and 616:
Page 617 and 618:
Page 619 and 620:
Page 621 and 622:
Page 623 and 624:
Page 625 and 626:
Page 627 and 628:
Page 629 and 630:
Page 631 and 632:
Page 633 and 634:
Page 635 and 636:
Page 637 and 638:
Page 639 and 640:
Page 641 and 642:
Page 643 and 644:
Page 645 and 646:
Page 647 and 648:
show all

11th ICRS Abstract book - Nova Southeastern University

You also want an ePaper? Increase the reach of your titles

Delete template?

Save as template?