World Congress of Malacology Antwerp ... - Unitas Malacologica
World Congress of Malacology Antwerp ... - Unitas Malacologica World Congress of Malacology Antwerp ... - Unitas Malacologica
Evaluation of Neogastropoda of the Cretaceous, their taxonomy and relation based on the morphology of their protoconch Bandel, Klaus Geologisch Paläontologisches Institut, University of Hamburg, Hamburg, Germany, Email: klausbandel@yahoo.com Traditionally many families of the Neogastropoda have been recognized among the fossil Late Cretaceous species based on the morphology of their adult shell. The excellent preservation of shells from the Campanian and Maastrichtian Ripley Formation of Mississippi and Tennessee allowed to examine the protoconch of many of these taxa. In those species with shell of a planktotrophic veliger a comparison with larvae of different families of modern Latrogastropoda provides no evidence for a close relation between fossil and recent species. Obviously the closeness in morphology in adult shell shape is due to convergence. The study also revealed that many of the taxa of the Ripley Formation have no living counterparts but represent groups that have become extinct since, mostly connected to the K/T event. The Pyrifusidae are united by the character of their protoconch and may represent stem group Neogastropoda. They can be split into several subfamilies according to the shape of their teleoconch. Their larval shells resembles in general shape and ornament some found among modern species of Muricidae, Buccinidae or Conidae with little ornament and a median projection of the final apertural outer lip, but they differ from the modern species by an indistinct apertural margin and gradational transition of larval shell into the teleoconch. Some of the fossil taxa that have been assumed to represent Neogastropoda are actually related to groups of the Neomesogastropoda. The protoconch of Sarganidae and Moreidae is for example lowly coiled with rounded whorls and its apertural margin not lobed, in contrast to the elongate conical protoconch of most modern Neogastropoda as well as that of the Pyrifusidae. Similar shapes are found among modern Ficidae, Capulidae or Eratiodae of the Neomesogastropoda. Cretaceous Paladmetidae have a larval shells that connect in shape and ornament of rectangles to that of the Tonnoidea, but also to the problematic fossil Colombellinidae. The early appearance of the Naticidae, Cypraeidae and Calyptraeidae during the Late Cretaceous provides evidence of the origin of the Latrogastropoda and both their branches Neogastropoda and Neomesogastropoda before Aptian/Albian time about 100 Million years ago. But their representatives are conspicuously absent from all well known Early Cretaceous faunal assemblages. Stem group Latrogastropoda have been suggested in the Maturifusidae of the Jurassic to Cretaceous and the Purpurinidae of the Jurassic to Triassic, but their protoconch is not close to that of the Ripley gastropods. The Pyrifusidae of the Late Cretaceous may have given rise to some of the modern groups of the Neogastropoda such as Volutidae still during the Late Cretaceous, while many of the taxa of the Neogastropoda appear within the Paleogene and their fossil species are usually recognized by the characters of their protoconch. Comparative anatomy of selected Philippine Cone snails (Neogastropoda) Baoanan, Zenaida Gutay 1 , Cruz, Lourdes J. 2 ; Pagulayan, Roberto C. 3 ; Lagunzad, Daniel A. 4 1. Faculty, Department of Biology, College of Science, University of the Philippines Baguio, Baguio City and Ph.D. Candidate, Institute of Biology, College of Science, University of the Philippines Diliman, Quezon City, Philippines, Email: zbaoanan@yahoo.com 2. Marine Science Institute, College of Science, University of the Philippines Diliman, Quezon City, Philippines, Email: lulycruzj@yahoo.com 3. Angeles University Foundation, Angeles City, Pampanga, Philippines, Email: roberto_pagulayan@yahoo.com 4. Institute of Biology, College of Science, University of the Philippines, Diliman, Quezon City, Philippines, Email: dalagunzad@yahoo.com 16
Conus (cone snails) is an unusually species-rich genus of predatory and venomous tropical marine gastropods. Comparative analysis on the anatomy of selected Philippine cone snails with different feeding types was done to elucidate the usefulness of anatomical characters in inferring phylogenetic relationships within this genus. Standard dissection supplemented with serial histological sections was used to obtain anatomical data sets from six species of Conus (C. imperialis, C. ebraeus, C. miles, C. textile, C. magus, and C. striatus) and two outgroups (Lophiotoma acuta and L. abreviata). Characters were taken from the adult shell, operculum, osphradium, ctenidium, male reproductive system, venom apparatus including the salivary gland, and radula. A consensus tree of selected Conus species was produced based on 2 most parsimonious trees generated by PAUP* 4.0 (Swofford 1998) from initial data consisting of 40 morphological characters with 95 character states. Preliminary analysis indicates that C. ebraeus has more characters shared with the outgroup. The tree has a branching pattern that supports the grouping of Conus into different feeding types with 97% bootstrap support based on 1000 replicates. Application of a 16S rDNA barcode to diagnose pest Arion species in the U.S.A. Barr, Norman 1 ; Cook, Amanda 1 ; Elder, Peggy 2 , Molongoski, John 2 , Prasher, Douglas 2 ; Robinson, David 3 1. USDA-APHIS-PPQ, Center for Plant Health Science and Technology (CPHST), Pest Detection Diagnostics and Management Laboratory, Edinburg, TX 78541, USA, Email: Norman.B.Barr@aphis.usda.gov 2. USDA-APHIS-PPQ, CPHST, Pest Survey Detection and Exclusion Laboratory, Otis, MA 02542, USA, Email: John.J.Molongoski@aphis.usda.gov 3. USDA-APHIS-PPQ, Department of Malacology, Academy of Natural Sciences, 1900 Benjamin Franklin Parkway, Philadelphia, PA 19130, USA, Email: robinson@acnatsci.org The utility of a DNA barcode using the ribosomal 16S gene is examined for Arion species by characterizing genetic variation within and between taxa. Comparison of variation within Arion DNA sequences indicates that 16S is as variable as the commonly used barcode region of cytochrome oxidase I. Analytical sensitivity (measured by PCR success), however, was greater for the 16S marker. Based on 16S variation, a reference database comprising over 270 DNA sequences and over 20 species was generated and used to analyze query sequences from slugs collected within the United States or intercepted at U.S. ports of entry. As expected, the total number of “positive” taxonomic identifications varied when different barcode interpretive rules were applied and the success of the barcode (i.e. proportion of identifications) was greater when queried slugs were from North America. The relevance of this barcode tool to pest quarantine programs and aspects of its implementation are discussed. 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCCD) affects shell mineralization of the freshwater bivalve Anodonta cygnea L. Barrias, Cláudia 1 ; Silva, Luís 1 ; Lemos, Carolina 1 ; Oliveira, Eduardo 1 ; Rebelo da Costa, Augusta 1,2 1. Laboratório de Fisiologia dos Gâmetas e Transporte (CECA-UP), Vairão/Portugal Email: ladybarrias@hotmail.com; carolina.c.lemos@sapo.pt; eduardoftoliveira@gmail.com; luis_silva519@hotmail.com 2. Laboratório de Fisiologia/ Dpt. Imuno-Fisiologia e Farmacologia, (ICBAS-UP), Porto, Portugal Email: a.rebelo@netcabo.pt 17
- Page 45 and 46: 12:50 - 14:00 Lunch + AMS Conservat
- Page 47 and 48: THURSDAY 19 JULY MOLLUSCS AS MODELS
- Page 49 and 50: 17:10 - 17:30 Germany’s next top
- Page 51 and 52: OPEN SESSION: MARINE ECOLOGY Chair:
- Page 53 and 54: OPEN SESSION: FRESHWATER MOLLUSCS C
- Page 55 and 56: 12:30 - 12:50 Phylogenetics of the
- Page 57 and 58: 12:50 - 14:00 Lunch + AMS Students
- Page 59 and 60: 12:10 - 12:30 Comparative anatomy o
- Page 61 and 62: 12:30 - 12:50 Threshold dimorphism
- Page 63 and 64: 12:50 - 14:00 Lunch + AMS Students
- Page 65 and 66: POSTERS In alphabetical order of th
- Page 67 and 68: Correlates of endemism and biogeogr
- Page 69 and 70: Extreme variability in the radula o
- Page 71 and 72: Development of an initial conservat
- Page 73 and 74: Cell and tissue biology of the muss
- Page 75 and 76: Fresh water mollusks of the Azores:
- Page 77 and 78: Ecological character displacement a
- Page 79 and 80: Preliminary studies on the occurren
- Page 81 and 82: ABSTRACTS Contribution to the revis
- Page 83 and 84: In 2006 I sampled 45 sites in the 1
- Page 85 and 86: share morphological features of the
- Page 87 and 88: Freshwater bivalve biodiversity: ne
- Page 89 and 90: Hidden genetic diversity in cephalo
- Page 91 and 92: How many unionoid taxa live in the
- Page 93 and 94: etween springs, 3) and reduction of
- Page 95: The effects of salinity changes on
- Page 99 and 100: Cytogenetic damage in aquatic mollu
- Page 101 and 102: fertilization as the predominant ma
- Page 103 and 104: Spatio-temporal and biomass dynamic
- Page 105 and 106: little attention. Molluscs are bare
- Page 107 and 108: into one taxon, since they form a w
- Page 109 and 110: near-complete outline. A conservati
- Page 111 and 112: Opportunities to acquire important
- Page 113 and 114: The Santa Barbara Museum of Natural
- Page 115 and 116: Unravelling a taxonomic tangle and
- Page 117 and 118: soil type and geological age) for P
- Page 119 and 120: Heterometric autoregulation in the
- Page 121 and 122: Snails from America’s heartland:
- Page 123 and 124: congener R. guerinii Reclùz, 1843.
- Page 125 and 126: Gastropod species as model organism
- Page 127 and 128: snails interact they may, co-operat
- Page 129 and 130: Evolution of spermatophore ornament
- Page 131 and 132: Invasive freshwater species Sinanod
- Page 133 and 134: Can response to water flow explain
- Page 135 and 136: A DNA-based phylogeny resolves dive
- Page 137 and 138: and I. rositai. Besides, their phyl
- Page 139 and 140: The allozyme data showed no sign of
- Page 141 and 142: We have used mitochondrial COI DNA
- Page 143 and 144: phylogenetic status of the Sicilian
- Page 145 and 146: asal origin of species from Sulawes
Evaluation <strong>of</strong> Neogastropoda <strong>of</strong> the Cretaceous, their taxonomy and relation based on the<br />
morphology <strong>of</strong> their protoconch<br />
Bandel, Klaus<br />
Geologisch Paläontologisches Institut, University <strong>of</strong> Hamburg, Hamburg, Germany,<br />
Email: klausbandel@yahoo.com<br />
Traditionally many families <strong>of</strong> the Neogastropoda have been recognized among the fossil Late<br />
Cretaceous species based on the morphology <strong>of</strong> their adult shell. The excellent preservation <strong>of</strong> shells<br />
from the Campanian and Maastrichtian Ripley Formation <strong>of</strong> Mississippi and Tennessee allowed to<br />
examine the protoconch <strong>of</strong> many <strong>of</strong> these taxa. In those species with shell <strong>of</strong> a planktotrophic veliger<br />
a comparison with larvae <strong>of</strong> different families <strong>of</strong> modern Latrogastropoda provides no evidence for a<br />
close relation between fossil and recent species. Obviously the closeness in morphology in adult shell<br />
shape is due to convergence. The study also revealed that many <strong>of</strong> the taxa <strong>of</strong> the Ripley Formation<br />
have no living counterparts but represent groups that have become extinct since, mostly connected to<br />
the K/T event. The Pyrifusidae are united by the character <strong>of</strong> their protoconch and may represent<br />
stem group Neogastropoda. They can be split into several subfamilies according to the shape <strong>of</strong> their<br />
teleoconch. Their larval shells resembles in general shape and ornament some found among modern<br />
species <strong>of</strong> Muricidae, Buccinidae or Conidae with little ornament and a median projection <strong>of</strong> the final<br />
apertural outer lip, but they differ from the modern species by an indistinct apertural margin and<br />
gradational transition <strong>of</strong> larval shell into the teleoconch. Some <strong>of</strong> the fossil taxa that have been<br />
assumed to represent Neogastropoda are actually related to groups <strong>of</strong> the Neomesogastropoda. The<br />
protoconch <strong>of</strong> Sarganidae and Moreidae is for example lowly coiled with rounded whorls and its<br />
apertural margin not lobed, in contrast to the elongate conical protoconch <strong>of</strong> most modern<br />
Neogastropoda as well as that <strong>of</strong> the Pyrifusidae. Similar shapes are found among modern Ficidae,<br />
Capulidae or Eratiodae <strong>of</strong> the Neomesogastropoda. Cretaceous Paladmetidae have a larval shells that<br />
connect in shape and ornament <strong>of</strong> rectangles to that <strong>of</strong> the Tonnoidea, but also to the problematic<br />
fossil Colombellinidae. The early appearance <strong>of</strong> the Naticidae, Cypraeidae and Calyptraeidae during<br />
the Late Cretaceous provides evidence <strong>of</strong> the origin <strong>of</strong> the Latrogastropoda and both their branches<br />
Neogastropoda and Neomesogastropoda before Aptian/Albian time about 100 Million years ago. But<br />
their representatives are conspicuously absent from all well known Early Cretaceous faunal<br />
assemblages. Stem group Latrogastropoda have been suggested in the Maturifusidae <strong>of</strong> the Jurassic to<br />
Cretaceous and the Purpurinidae <strong>of</strong> the Jurassic to Triassic, but their protoconch is not close to that <strong>of</strong><br />
the Ripley gastropods. The Pyrifusidae <strong>of</strong> the Late Cretaceous may have given rise to some <strong>of</strong> the<br />
modern groups <strong>of</strong> the Neogastropoda such as Volutidae still during the Late Cretaceous, while many<br />
<strong>of</strong> the taxa <strong>of</strong> the Neogastropoda appear within the Paleogene and their fossil species are usually<br />
recognized by the characters <strong>of</strong> their protoconch.<br />
Comparative anatomy <strong>of</strong> selected Philippine Cone snails (Neogastropoda)<br />
Baoanan, Zenaida Gutay 1 , Cruz, Lourdes J. 2 ; Pagulayan, Roberto C. 3 ;<br />
Lagunzad, Daniel A. 4<br />
1. Faculty, Department <strong>of</strong> Biology, College <strong>of</strong> Science, University <strong>of</strong> the Philippines<br />
Baguio, Baguio City and Ph.D. Candidate, Institute <strong>of</strong> Biology, College <strong>of</strong> Science,<br />
University <strong>of</strong> the Philippines Diliman, Quezon City, Philippines,<br />
Email: zbaoanan@yahoo.com<br />
2. Marine Science Institute, College <strong>of</strong> Science, University <strong>of</strong> the Philippines<br />
Diliman, Quezon City, Philippines,<br />
Email: lulycruzj@yahoo.com<br />
3. Angeles University Foundation, Angeles City, Pampanga, Philippines,<br />
Email: roberto_pagulayan@yahoo.com<br />
4. Institute <strong>of</strong> Biology, College <strong>of</strong> Science, University <strong>of</strong> the Philippines, Diliman, Quezon City,<br />
Philippines,<br />
Email: dalagunzad@yahoo.com<br />
16