2016-09 R&C Newsletter
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1 Creating a Species Inventory for a Marine Protected Area: the Missing
Katherine R. Rice NOAA Species Inventory Project Spring 2018 Creating a Species Inventory for a Marine Protected Area: The Missing Piece for Effective Ecosystem-Based Marine Management Katherine R. Rice ABSTRACT Over the past decade, ecosystem-based management has been incorporated into many marine- management administrations as a marine-conservation tool, driven with the objective to predict, evaluate and possibly mitigate the impacts of a warming and acidifying ocean, and a coastline increasingly subject to anthropogenic control. The NOAA Office of National Marine Sanctuaries (ONMS) is one such administration, and was instituted “to serve as the trustee for a network of 13 underwater parks encompassing more than 600,000 square miles of marine and Great Lakes waters from Washington state to the Florida Keys, and from Lake Huron to American Samoa” (NOAA, 2015). The management regimes for nearly all national marine sanctuaries, as well as other marine protected areas, have the goal of managing and maintaining biodiversity within the sanctuary. Yet none of those sanctuaries have an inventory of their known species nor a standardized protocol for measuring or monitoring species biodiversity. Here, I outline the steps required to compile a species inventory for an MPA, but also describe some of stumbling blocks that one might encounter along the way and offer suggestions on how to handle these issues (see Appendix A: Process for Developing the MBNMS Species Inventory (PD-MBNMS)). This project consists of three research objectives: 1. Determining what species inventory efforts exist, how they operate, and their advantages and disadvantages 2. Determining the process of creating a species inventory 3. -
The Origin and Early Evolution of Dinosaurs
Biol. Rev. (2010), 85, pp. 55–110. 55 doi:10.1111/j.1469-185X.2009.00094.x The origin and early evolution of dinosaurs Max C. Langer1∗,MartinD.Ezcurra2, Jonathas S. Bittencourt1 and Fernando E. Novas2,3 1Departamento de Biologia, FFCLRP, Universidade de S˜ao Paulo; Av. Bandeirantes 3900, Ribeir˜ao Preto-SP, Brazil 2Laboratorio de Anatomia Comparada y Evoluci´on de los Vertebrados, Museo Argentino de Ciencias Naturales ‘‘Bernardino Rivadavia’’, Avda. Angel Gallardo 470, Cdad. de Buenos Aires, Argentina 3CONICET (Consejo Nacional de Investigaciones Cient´ıficas y T´ecnicas); Avda. Rivadavia 1917 - Cdad. de Buenos Aires, Argentina (Received 28 November 2008; revised 09 July 2009; accepted 14 July 2009) ABSTRACT The oldest unequivocal records of Dinosauria were unearthed from Late Triassic rocks (approximately 230 Ma) accumulated over extensional rift basins in southwestern Pangea. The better known of these are Herrerasaurus ischigualastensis, Pisanosaurus mertii, Eoraptor lunensis,andPanphagia protos from the Ischigualasto Formation, Argentina, and Staurikosaurus pricei and Saturnalia tupiniquim from the Santa Maria Formation, Brazil. No uncontroversial dinosaur body fossils are known from older strata, but the Middle Triassic origin of the lineage may be inferred from both the footprint record and its sister-group relation to Ladinian basal dinosauromorphs. These include the typical Marasuchus lilloensis, more basal forms such as Lagerpeton and Dromomeron, as well as silesaurids: a possibly monophyletic group composed of Mid-Late Triassic forms that may represent immediate sister taxa to dinosaurs. The first phylogenetic definition to fit the current understanding of Dinosauria as a node-based taxon solely composed of mutually exclusive Saurischia and Ornithischia was given as ‘‘all descendants of the most recent common ancestor of birds and Triceratops’’. -
The Sauropodomorph Biostratigraphy of the Elliot Formation of Southern Africa: Tracking the Evolution of Sauropodomorpha Across the Triassic–Jurassic Boundary
Editors' choice The sauropodomorph biostratigraphy of the Elliot Formation of southern Africa: Tracking the evolution of Sauropodomorpha across the Triassic–Jurassic boundary BLAIR W. MCPHEE, EMESE M. BORDY, LARA SCISCIO, and JONAH N. CHOINIERE McPhee, B.W., Bordy, E.M., Sciscio, L., and Choiniere, J.N. 2017. The sauropodomorph biostratigraphy of the Elliot Formation of southern Africa: Tracking the evolution of Sauropodomorpha across the Triassic–Jurassic boundary. Acta Palaeontologica Polonica 62 (3): 441–465. The latest Triassic is notable for coinciding with the dramatic decline of many previously dominant groups, followed by the rapid radiation of Dinosauria in the Early Jurassic. Among the most common terrestrial vertebrates from this time, sauropodomorph dinosaurs provide an important insight into the changing dynamics of the biota across the Triassic–Jurassic boundary. The Elliot Formation of South Africa and Lesotho preserves the richest assemblage of sauropodomorphs known from this age, and is a key index assemblage for biostratigraphic correlations with other simi- larly-aged global terrestrial deposits. Past assessments of Elliot Formation biostratigraphy were hampered by an overly simplistic biozonation scheme which divided it into a lower “Euskelosaurus” Range Zone and an upper Massospondylus Range Zone. Here we revise the zonation of the Elliot Formation by: (i) synthesizing the last three decades’ worth of fossil discoveries, taxonomic revision, and lithostratigraphic investigation; and (ii) systematically reappraising the strati- graphic provenance of important fossil locations. We then use our revised stratigraphic information in conjunction with phylogenetic character data to assess morphological disparity between Late Triassic and Early Jurassic sauropodomorph taxa. Our results demonstrate that the Early Jurassic upper Elliot Formation is considerably more taxonomically and morphologically diverse than previously thought. -
(Hermania) Scabra (Miiller
BASTERIA, 59: 97-104, 1996 Philine from the Miocene of aquila sp. nov. Winterswijk (Miste) (Gastropoda, Opisthobranchia) J. van der Linden Frankenslag 176, 2582 HZ Den Haag, The Netherlands & A.W. Janssen Nationaal Natuurhistorisch Museum, P.O. Box 9517, 2300 RA Leiden, The Netherlands Philine is described from the Miocene Oxlundian; Breda Forma- aquila sp. nov. (Hemmoorian, Aalten Miste of The tion, Member, Bed) Winterswijk (Miste), Netherlands (Gelderland pro- Pliocene Recent P. scabra vince). The shell of the new species closely resembles that of the to and P. & but differs in (Müller, 1776), P. sagra (d’Orbigny, 1841) sp. 1 De Jong Coomans, 1988, details ofshape and sculpture. Key words: Gastropoda, Opisthobranchia, Philinidae, Miocene, taxonomy, new species. various In connection with a revision of the rich material of Recent Philinidaefrom in the expeditions, present the collections of Nationaal Natuurhistorisch Museum of North Sea Basin (Leiden), some fossil samples from the Miocene and Pliocene the were studied for comparison. Specimens identified as Philine (Hermania) scabra (Miiller, 1776) byjanssen (1984: 374, pi. 19 fig. 12) were found to differ considerably from the Recent species. They are here introduced as a new species. The fossil material is housed in the Palaeontology Department (Cainozoic Mollusca) of the Nationaal Natuurhistorisch Museum at Leiden (formerly Rijksmuseum van Geologie en Mineralogie) and is here referred to with RGM registration numbers. Material from the Zoological Museum, Amsterdam is indicated with ZMA. Philine aquila sp. nov. (figs. 1-3) 1984 Philine (Hermania) scabra (Miiller, 1776) —Janssen, 1984: 374, pi. 19 fig. 12 (non Miiller). — RGM 1.9 Type material. -
West Antarctica: Tectonics and Paleogeography
Chapter 2 West Antarctica: Tectonics and Paleogeography The origin of West Antarctica (WANT) can be traced back to the Terra Australis orogenesis that began between 520 Ma and 510 Ma—shortly after the terminal suturing of Gondwana (Boger 2011). The onset of this event was responsible for the termination of passive margin sedimentation along much of the Pacific margin of Gondwana and marks the beginning of widespread and broadly coeval deforma- tion and arc-type plutonism. It also began a long-lived process of accretion that added much of the crust that defines eastern Australia, West Antarctica (domain 5 of Boger 2011, Fig. 2.1), and western South America (Cawood 2005, 2009). Post-Gondwana accretionary growth—the Terra Australis and Gondwanide Orogenies—The suturing of the West Gondwana and Australo–Antarctic plates along the Kuunga Orogen brought to an end the long-lived process of convergence between the pre-collision components of Gondwana. The result was a reconfigura- tion of the early to middle Cambrian plate system and the consequent transfer of ocean floor consumption from between the pre-Gondwana cratons to the outboard Pacific margin of newly formed Gondwana supercontinent (Cawood2005 ). This led to the establishment of the accretionary Terra Austrais Orogen (Cawood 2005), a general name given to the orogenic belt that stretched continuously from north- ern South America to northern Australia and which began in the early to middle Cambrian and lasted until the late Carboniferous. In Antarctica Terra Australis (Ross) orogenesis also deformed and variably metamorphosed the pre-Gondwana passive margin (Fig. 2.2). The Gondwana supercontinent underwent a sequential fragmentation over approximately 165 Ma. -
OREGON ESTUARINE INVERTEBRATES an Illustrated Guide to the Common and Important Invertebrate Animals
OREGON ESTUARINE INVERTEBRATES An Illustrated Guide to the Common and Important Invertebrate Animals By Paul Rudy, Jr. Lynn Hay Rudy Oregon Institute of Marine Biology University of Oregon Charleston, Oregon 97420 Contract No. 79-111 Project Officer Jay F. Watson U.S. Fish and Wildlife Service 500 N.E. Multnomah Street Portland, Oregon 97232 Performed for National Coastal Ecosystems Team Office of Biological Services Fish and Wildlife Service U.S. Department of Interior Washington, D.C. 20240 Table of Contents Introduction CNIDARIA Hydrozoa Aequorea aequorea ................................................................ 6 Obelia longissima .................................................................. 8 Polyorchis penicillatus 10 Tubularia crocea ................................................................. 12 Anthozoa Anthopleura artemisia ................................. 14 Anthopleura elegantissima .................................................. 16 Haliplanella luciae .................................................................. 18 Nematostella vectensis ......................................................... 20 Metridium senile .................................................................... 22 NEMERTEA Amphiporus imparispinosus ................................................ 24 Carinoma mutabilis ................................................................ 26 Cerebratulus californiensis .................................................. 28 Lineus ruber ......................................................................... -
Benthic Data Sheet
DEMERSAL OTTER/BEAM TRAWL DATA SHEET RESEARCH VESSEL_____________________(1/20/13 Version*) CLASS__________________;DATE_____________;NAME:___________________________; DEVICE DETAILS_________ LOCATION (OVERBOARD): LAT_______________________; LONG______________________________ LOCATION (AT DEPTH): LAT_______________________; LONG_____________________________; DEPTH___________ LOCATION (START UP): LAT_______________________; LONG______________________________;.DEPTH__________ LOCATION (ONBOARD): LAT_______________________; LONG______________________________ TIME: IN______AT DEPTH_______START UP_______SURFACE_______.DURATION OF TRAWL________; SHIP SPEED__________; WEATHER__________________; SEA STATE__________________; AIR TEMP______________ SURFACE TEMP__________; PHYS. OCE. NOTES______________________; NOTES_______________________________ INVERTEBRATES Phylum Porifera Order Pennatulacea (sea pens) Class Calcarea __________________________________ Family Stachyptilidae Class Demospongiae (Vase sponge) _________________ Stachyptilum superbum_____________________ Class Hexactinellida (Hyalospongia- glass sponge) Suborder Subsessiliflorae Subclass Hexasterophora Family Pennatulidae Order Hexactinosida Ptilosarcus gurneyi________________________ Family Aphrocallistidae Family Virgulariidae Aphrocallistes vastus ______________________ Acanthoptilum sp. ________________________ Other__________________________________________ Stylatula elongata_________________________ Phylum Cnidaria (Coelenterata) Virgularia sp.____________________________ Other_______________________________________ -
Pdumbase: a Transcriptome Database and Research Tool for Platynereis
Chou et al. BMC Genomics (2018) 19:618 https://doi.org/10.1186/s12864-018-4987-0 DATABASE Open Access PdumBase: a transcriptome database and research tool for Platynereis dumerilii and early development of other metazoans Hsien-Chao Chou1,2†, Natalia Acevedo-Luna1†, Julie A. Kuhlman1 and Stephan Q. Schneider1* Abstract Background: The marine polychaete annelid Platynereis dumerilii has recently emerged as a prominent organism for the study of development, evolution, stem cells, regeneration, marine ecology, chronobiology and neurobiology within metazoans. Its phylogenetic position within the spiralian/ lophotrochozoan clade, the comparatively high conservation of ancestral features in the Platynereis genome, and experimental access to any stage within its life cycle, make Platynereis an important model for elucidating the complex regulatory and functional molecular mechanisms governing early development, later organogenesis, and various features of its larval and adult life. High resolution RNA- seq gene expression data obtained from specific developmental stages can be used to dissect early developmental mechanisms. However, the potential for discovery of these mechanisms relies on tools to search, retrieve, and compare genome-wide information within Platynereis, and across other metazoan taxa. Results: To facilitate exploration and discovery by the broader scientific community, we have developed a web-based, searchable online research tool, PdumBase, featuring the first comprehensive transcriptome database for Platynereis dumerilii during early stages of development (2 h ~ 14 h). Our database also includes additional stages over the P. dumerilii life cycle and provides access to the expression data of 17,213 genes (31,806 transcripts) along with annotation information sourced from Swiss-Prot, Gene Ontology, KEGG pathways, Pfam domains, TmHMM, SingleP, and EggNOG orthology. -
Abstract Volume
ABSTRACT VOLUME August 11-16, 2019 1 2 Table of Contents Pages Acknowledgements……………………………………………………………………………………………...1 Abstracts Symposia and Contributed talks……………………….……………………………………………3-225 Poster Presentations…………………………………………………………………………………226-291 3 Venom Evolution of West African Cone Snails (Gastropoda: Conidae) Samuel Abalde*1, Manuel J. Tenorio2, Carlos M. L. Afonso3, and Rafael Zardoya1 1Museo Nacional de Ciencias Naturales (MNCN-CSIC), Departamento de Biodiversidad y Biologia Evolutiva 2Universidad de Cadiz, Departamento CMIM y Química Inorgánica – Instituto de Biomoléculas (INBIO) 3Universidade do Algarve, Centre of Marine Sciences (CCMAR) Cone snails form one of the most diverse families of marine animals, including more than 900 species classified into almost ninety different (sub)genera. Conids are well known for being active predators on worms, fishes, and even other snails. Cones are venomous gastropods, meaning that they use a sophisticated cocktail of hundreds of toxins, named conotoxins, to subdue their prey. Although this venom has been studied for decades, most of the effort has been focused on Indo-Pacific species. Thus far, Atlantic species have received little attention despite recent radiations have led to a hotspot of diversity in West Africa, with high levels of endemic species. In fact, the Atlantic Chelyconus ermineus is thought to represent an adaptation to piscivory independent from the Indo-Pacific species and is, therefore, key to understanding the basis of this diet specialization. We studied the transcriptomes of the venom gland of three individuals of C. ermineus. The venom repertoire of this species included more than 300 conotoxin precursors, which could be ascribed to 33 known and 22 new (unassigned) protein superfamilies, respectively. Most abundant superfamilies were T, W, O1, M, O2, and Z, accounting for 57% of all detected diversity. -
A Probable Oligochaete from an Early Triassic Lagerstätte of the Southern Cis-Urals and Its Evolutionary Implications
Editors' choice A probable oligochaete from an Early Triassic Lagerstätte of the southern Cis-Urals and its evolutionary implications DMITRY E. SHCHERBAKOV, TARMO TIMM, ALEXANDER B. TZETLIN, OLEV VINN, and ANDREY Y. ZHURAVLEV Shcherbakov, D.E., Timm, T., Tzetlin, A.B., Vinn, O., and Zhuravlev, A.Y. 2020. A probable oligochaete from an Early Triassic Lagerstätte of the southern Cis-Urals and its evolutionary implications. Acta Palaeontologica Polonica 65 (2): 219–233. Oligochaetes, despite their important role in terrestrial ecosystems and a tremendous biomass, are extremely rare fossils. The palaeontological record of these worms is restricted to some cocoons, presumable trace fossils and a few body fossils the most convincing of which are discovered in Mesozoic and Cenozoic strata. The Olenekian (Lower Triassic) siliciclastic lacustrine Petropavlovka Lagerstätte of the southern Cis-Urals yields a number of extraordinary freshwater fossils including an annelid. The segmented body with a secondary annulation of this fossil, a subtriangular prostomium, a relatively thick layered body wall and, possibly, the presence of a genital region point to its oligochaete affinities. Other fossil worms which have been ascribed to clitellates are reviewed and, with a tentative exception of two Pennsylvanian finds, affinities of any pre-Mesozoic forms to clitellate annelids are rejected. The new fossil worm allows tracing of a persuasive oligochaete record to the lowermost Mesozoic and confirms a plausibility of the origin of this annelid group in freshwater conditions. Key words: Annelida, Clitellata, Oligochaeta, Mesozoic, Lagerstätte, Russia. Dmitry E. Shcherbakov [[email protected]], Borissiak Palaeontological Institute, Russian Academy of Sciences, Profso- yuz naya St 123, Moscow 117647, Russia. -
Lyons SCIENCE 2021 the Influence of Juvenile Dinosaurs SUPPL.Pdf
science.sciencemag.org/content/371/6532/941/suppl/DC1 Supplementary Materials for The influence of juvenile dinosaurs on community structure and diversity Katlin Schroeder*, S. Kathleen Lyons, Felisa A. Smith *Corresponding author. Email: [email protected] Published 26 February 2021, Science 371, 941 (2021) DOI: 10.1126/science.abd9220 This PDF file includes: Materials and Methods Supplementary Text Figs. S1 and S2 Tables S1 to S7 References Other Supplementary Material for this manuscript includes the following: (available at science.sciencemag.org/content/371/6532/941/suppl/DC1) MDAR Reproducibility Checklist (PDF) Materials and Methods Data Dinosaur assemblages were identified by downloading all vertebrate occurrences known to species or genus level between 200Ma and 65MA from the Paleobiology Database (PaleoDB 30 https://paleobiodb.org/#/ download 6 August, 2018). Using associated depositional environment and taxonomic information, the vertebrate database was limited to only terrestrial organisms, excluding amphibians, pseudosuchians, champsosaurs and ichnotaxa. Taxa present in formations were confirmed against the most recent available literature, as of November, 2020. Synonymous taxa or otherwise duplicated taxa were removed. Taxa that could not be identified to genus level 35 were included as “Taxon X”. GPS locality data for all formations between 200MA and 65MA was downloaded from PaleoDB to create a minimally convex polygon for each possible formation. Any attempt to recreate local assemblages must include all potentially interacting species, while excluding those that would have been separated by either space or time. We argue it is 40 acceptable to substitute formation for home range in the case of non-avian dinosaurs, as range increases with body size. -
A New Cryptic Species of Neanthes (Annelida: Phyllodocida: Nereididae)
RAFFLES BULLETIN OF ZOOLOGY 2015 RAFFLES BULLETIN OF ZOOLOGY Supplement No. 31: 75–95 Date of publication: 10 July 2015 http://zoobank.org/urn:lsid:zoobank.org:pub:A039A3A6-C05B-4F36-8D7F-D295FA236C6B A new cryptic species of Neanthes (Annelida: Phyllodocida: Nereididae) from Singapore confused with Neanthes glandicincta Southern, 1921 and Ceratonereis (Composetia) burmensis (Monro, 1937) Yen-Ling Lee1* & Christopher J. Glasby2 Abstract. A new cryptic species of Neanthes (Nereididae), N. wilsonchani, new species, is described from intertidal mudflats of eastern Singapore. The new species was confused with both Ceratonereis (Composetia) burmensis (Monro, 1937) and Neanthes glandicincta Southern, 1921, which were found to be conspecific with the latter name having priority. Neanthes glandicincta is newly recorded from Singapore, its reproductive forms (epitokes) are redescribed, and Singapore specimens are compared with topotype material from India. The new species can be distinguished from N. glandicincta by slight body colour differences and by having fewer pharyngeal paragnaths in Areas II (4–8 vs 7–21), III (11–28 vs 30–63) and IV (1–9 vs 7–20), and in the total number of paragnaths for all Areas (16–41 vs 70–113). No significant differences were found in the morphology of the epitokes between the two species. The two species have largely non-overlapping distributions in Singapore; the new species is restricted to Pleistocene coastal alluvium in eastern Singapore, while N. glandicinta occurs in western Singapore as well as in Malaysia and westward to India. Key words. polychaete, new species, taxonomy, ragworm INTRODUCTION Both species are atypical members of their respective nominative genera: N.