Book Reviews Source: Copeia, 104(4):965-976
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LARVAL FORMS in ECHINODERMATA in Echinoderms
LARVAL FORMS IN ECHINODERMATA In echinoderms eggs and sperms are released in water and fertilization takes place in water forming zygote. Echinoderms are deuterostomes and hence cleavage is radial, holoblastic and indeterminate. The larvae hatch in water and feed and grow through successive larval stages to become adults. The larvae of echinoderms are bilaterally symmetrical but lose symmetry during metamorphosis. Different classes of echinoderms show structurally different larval stages and their comparisons can reveal their evolutionary ancestry. LARVAE OF ASTEROIDEA There are three larval stages in Asteroidea in the course of their development to adult stage. Early bipinnaria appears like hypothetical dipleurula. It has oval body without arms and ciliary bands for locomotion. It has well developed alimentary canal for feeding and grows to become bipinnaria. Bipinnaria larva possesses 5 pairs of ciliated arms which do not have any skeletal support inside. These arms are used for swimming in water while feeding on planktons. Preoral and postoral ciliary bands are also present. This larva resembles auricularia larva of Holothuroidea in general appearance. Brachiolaria larva is formed after 6-7 weeks of life and growth of bipinnaria. This larva is sedentary and remains attached to a hard substratum for which it possesses three brachiolarian arms having adhesive discs at the tip. Ciliated arms get reduced and become thin and functionless, while mouth, anus and gut are well developed. It has axocoel, hydocoel and somatocoel that later on give rise to water vascular system Development of starfish takes place inside the sedentary brachiolaria which ruptures and releases tiny starfish into water. LARVAE OF HOLOTHUROIDEA Class Holothuroidea demonstrate two larval stages, namely, auricularia and doliolaria larvae. -
The Conservation Biology of Tortoises
The Conservation Biology of Tortoises Edited by Ian R. Swingland and Michael W. Klemens IUCN/SSC Tortoise and Freshwater Turtle Specialist Group and The Durrell Institute of Conservation and Ecology Occasional Papers of the IUCN Species Survival Commission (SSC) No. 5 IUCN—The World Conservation Union IUCN Species Survival Commission Role of the SSC 3. To cooperate with the World Conservation Monitoring Centre (WCMC) The Species Survival Commission (SSC) is IUCN's primary source of the in developing and evaluating a data base on the status of and trade in wild scientific and technical information required for the maintenance of biological flora and fauna, and to provide policy guidance to WCMC. diversity through the conservation of endangered and vulnerable species of 4. To provide advice, information, and expertise to the Secretariat of the fauna and flora, whilst recommending and promoting measures for their con- Convention on International Trade in Endangered Species of Wild Fauna servation, and for the management of other species of conservation concern. and Flora (CITES) and other international agreements affecting conser- Its objective is to mobilize action to prevent the extinction of species, sub- vation of species or biological diversity. species, and discrete populations of fauna and flora, thereby not only maintain- 5. To carry out specific tasks on behalf of the Union, including: ing biological diversity but improving the status of endangered and vulnerable species. • coordination of a programme of activities for the conservation of biological diversity within the framework of the IUCN Conserva- tion Programme. Objectives of the SSC • promotion of the maintenance of biological diversity by monitor- 1. -
A New Record of the Persian Brook Salamander, Paradactylodon Persicus (Eiselt & Steiner, 1970) (Amphibia: Caudata: Hynobiidae) in Northern Iran
Bonn zoological Bulletin Volume 60 Issue 1 pp. 63–65 Bonn, May 2011 A new record of the Persian Brook Salamander, Paradactylodon persicus (Eiselt & Steiner, 1970) (Amphibia: Caudata: Hynobiidae) in northern Iran Faraham Ahmadzadeh1, 2*, Fatemeh Khanjani3, Aref Shadkam4 & Wolfgang Böhme2 1Department of Biodiversity and Ecosystem Management, Environmental Sciences Research Institute, Shahid Beheshti University, Evin, Tehran, G. C., Iran 2Herpetology Section, Zoologisches Forschungsmuseum Alexander Koenig (ZFMK), Adenauerallee 160, D-53113 Bonn, Germany 3Department of Habitat and Biodiversity, Faculty of Environment and Energy, Science and Research Branch, Islamic Azad University, Ponak, Tehran, Iran 4Department of Environment, Rezvan Shahr, Province Gilan, Iran *Corresponding Email address: [email protected]. INTRODUCTION The Persian Brook Salamander, Paradactylodon persicus 90 mm; tail length 120 mm; head large, 20 mm in length; (Eiselt & Steiner, 1970) is an endemic and poorly known vomerine teeth in two arch-shaped rows; snout rounded; species of northern Iran (Baloutch & Kami 1995; Kami fore and hind limbs with four digits; tail flattened later- 1999). It was originally described as Batrachuperus per- ally, with round-tapered end; dorsal head and body, as well sicus by Eiselt & Steiner (1970), but has been transferred as upper surface of tail brownish with yellow spots and to the genus Paradactylodon based on genetic studies by marblings; belly cream without pattern (Fig. 2a–b). Zhang et al. (2006). This species has been reported from two localities only: Weyser, southeast of Chalus, in Paradactylodon persicus inhabits the mountainous Mazandaran Province (36º 30´ 35” N and 51º 26´ 38” E) streams and brooks, with cool, fast-flowing water and Delmadeh village, southeast of Khalkhal, in Ardabil (Baloutch & Kami 1995; Kami 1999; Ahmadzadeh & Ka- Province (37º 22´ 34” N and 48º 47´ 35” E) (Kami 2004; mi 2009). -
Amphibiaweb's Illustrated Amphibians of the Earth
AmphibiaWeb's Illustrated Amphibians of the Earth Created and Illustrated by the 2020-2021 AmphibiaWeb URAP Team: Alice Drozd, Arjun Mehta, Ash Reining, Kira Wiesinger, and Ann T. Chang This introduction to amphibians was written by University of California, Berkeley AmphibiaWeb Undergraduate Research Apprentices for people who love amphibians. Thank you to the many AmphibiaWeb apprentices over the last 21 years for their efforts. Edited by members of the AmphibiaWeb Steering Committee CC BY-NC-SA 2 Dedicated in loving memory of David B. Wake Founding Director of AmphibiaWeb (8 June 1936 - 29 April 2021) Dave Wake was a dedicated amphibian biologist who mentored and educated countless people. With the launch of AmphibiaWeb in 2000, Dave sought to bring the conservation science and basic fact-based biology of all amphibians to a single place where everyone could access the information freely. Until his last day, David remained a tirelessly dedicated scientist and ally of the amphibians of the world. 3 Table of Contents What are Amphibians? Their Characteristics ...................................................................................... 7 Orders of Amphibians.................................................................................... 7 Where are Amphibians? Where are Amphibians? ............................................................................... 9 What are Bioregions? ..................................................................................10 Conservation of Amphibians Why Save Amphibians? ............................................................................. -
Can Unwanted Suburban Tortoises Rescue Native Hawaiian Plants?
CAN UNWANTED SUBURBAN TORTOISES RESCUE NATIVE HAWAIIAN PLANTS? by David A. Burney, James O. Juvik, Lida Pigott Burney, and Tomas Diagne 104 THE TORTOISE ・ 2012 hrough a series of coincidences, surplus pet tortoises in Hawaii may end up offering a partial solution to the seemingly insurmountable challenge posed by invasive plants in the Makauwahi Cave Reserve Ton Kaua`i. This has come about through a serendipitous intersection of events in Africa, the Mascarene Islands, North America, and Hawaii. The remote Hawaiian Islands were beyond the reach of naturally dispersing island tortoises, but the niches were apparently still there. Giant flightless ducks and geese evolved on these islands with tortoise-like beaks and other adaptations as terrestrial “meso-herbivores.” Dating of these remarkable fossil remains shows that they went extinct soon after the arrival of Polynesians at the beginning of the last millennium leaving the niches for large native herbivores entirely empty. Other native birds, including important plant pollinators, and some plant species have also suffered extinction in recent centuries. This trend accelerated after European settlement ecosystem services and a complex mix of often with the introduction of many invasive alien plants conflicting stakeholder interests clearly requires and the establishment of feral ungulate populations new paradigms and new tools. such as sheep, goats, cattle, and European swine, as Lacking any native mammalian herbivores, the well as other insidious invasives such as deer, rats, majority of the over 1,000 native Hawaiian plant mongoose, feral house cats, and even mosquitoes, species on the islands have been widely regarded which transmit avian malaria to a poorly resistant in the literature as singularly lacking in defensive native avifauna. -
Origins of Endemic Island Tortoises in the Western Indian Ocean: a Critique of the Human-Translocation Hypothesis
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2017 Origins of endemic island tortoises in the western Indian Ocean: a critique of the human-translocation hypothesis Hansen, Dennis M ; Austin, Jeremy J ; Baxter, Rich H ; de Boer, Erik J ; Falcón, Wilfredo ; Norder, Sietze J ; Rijsdijk, Kenneth F ; Thébaud, Christophe ; Bunbury, Nancy J ; Warren, Ben H Abstract: How do organisms arrive on isolated islands, and how do insular evolutionary radiations arise? In a recent paper, Wilmé et al. (2016a) argue that early Austronesians that colonized Madagascar from Southeast Asia translocated giant tortoises to islands in the western Indian Ocean. In the Mascarene Islands, moreover, the human-translocated tortoises then evolved and radiated in an endemic genus (Cylindraspis). Their proposal ignores the broad, established understanding of the processes leading to the formation of native island biotas, including endemic radiations. We find Wilmé et al.’s suggestion poorly conceived, using a flawed methodology and missing two critical pieces of information: the timing and the specifics of proposed translocations. In response, we here summarize the arguments thatcould be used to defend the natural origin not only of Indian Ocean giant tortoises but also of scores of insular endemic radiations world-wide. Reinforcing a generalist’s objection, the phylogenetic and ecological data on giant tortoises, and current knowledge of environmental and palaeogeographical history of the Indian Ocean, make Wilmé et al.’s argument even more unlikely. DOI: https://doi.org/10.1111/jbi.12893 Posted at the Zurich Open Repository and Archive, University of Zurich ZORA URL: https://doi.org/10.5167/uzh-131419 Journal Article Accepted Version Originally published at: Hansen, Dennis M; Austin, Jeremy J; Baxter, Rich H; de Boer, Erik J; Falcón, Wilfredo; Norder, Sietze J; Rijsdijk, Kenneth F; Thébaud, Christophe; Bunbury, Nancy J; Warren, Ben H (2017). -
Human Translocation As an Alternative Hypothesis to Explain the Presence of Giant Tortoises on Remote Islands in the Southwestern Indian Ocean
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/298072054 Human translocation as an alternative hypothesis to explain the presence of giant tortoises on remote islands in the Southwestern Indian Ocean ARTICLE in JOURNAL OF BIOGEOGRAPHY · MARCH 2016 Impact Factor: 4.59 · DOI: 10.1111/jbi.12751 READS 63 3 AUTHORS: Lucienne Wilmé Patrick Waeber Missouri Botanical Garden ETH Zurich 50 PUBLICATIONS 599 CITATIONS 37 PUBLICATIONS 113 CITATIONS SEE PROFILE SEE PROFILE Jörg U. Ganzhorn University of Hamburg 208 PUBLICATIONS 5,425 CITATIONS SEE PROFILE All in-text references underlined in blue are linked to publications on ResearchGate, Available from: Lucienne Wilmé letting you access and read them immediately. Retrieved on: 18 March 2016 Journal of Biogeography (J. Biogeogr.) (2016) PERSPECTIVE Human translocation as an alternative hypothesis to explain the presence of giant tortoises on remote islands in the south-western Indian Ocean Lucienne Wilme1,2,*, Patrick O. Waeber3 and Joerg U. Ganzhorn4 1School of Agronomy, Water and Forest ABSTRACT Department, University of Antananarivo, Giant tortoises are known from several remote islands in the Indian Ocean Madagascar, 2Missouri Botanical Garden, (IO). Our present understanding of ocean circulation patterns, the age of the Madagascar Research & Conservation Program, Madagascar, 3Forest Management islands, and the life history traits of giant tortoises makes it difficult to com- and Development, Department of prehend how these animals arrived -
A Synopsis of the Pre-Human Avifauna of the Mascarene Islands
– 195 – Paleornithological Research 2013 Proceed. 8th Inter nat. Meeting Society of Avian Paleontology and Evolution Ursula B. Göhlich & Andreas Kroh (Eds) A synopsis of the pre-human avifauna of the Mascarene Islands JULIAN P. HUME Bird Group, Department of Life Sciences, The Natural History Museum, Tring, UK Abstract — The isolated Mascarene Islands of Mauritius, Réunion and Rodrigues are situated in the south- western Indian Ocean. All are volcanic in origin and have never been connected to each other or any other land mass. Despite their comparatively close proximity to each other, each island differs topographically and the islands have generally distinct avifaunas. The Mascarenes remained pristine until recently, resulting in some documentation of their ecology being made before they rapidly suffered severe degradation by humans. The first major fossil discoveries were made in 1865 on Mauritius and on Rodrigues and in the late 20th century on Réunion. However, for both Mauritius and Rodrigues, the documented fossil record initially was biased toward larger, non-passerine bird species, especially the dodo Raphus cucullatus and solitaire Pezophaps solitaria. This paper provides a synopsis of the fossil Mascarene avifauna, which demonstrates that it was more diverse than previously realised. Therefore, as the islands have suffered severe anthropogenic changes and the fossil record is far from complete, any conclusions based on present avian biogeography must be viewed with caution. Key words: Mauritius, Réunion, Rodrigues, ecological history, biogeography, extinction Introduction ily described or illustrated in ships’ logs and journals, which became the source material for The Mascarene Islands of Mauritius, Réunion popular articles and books and, along with col- and Rodrigues are situated in the south-western lected specimens, enabled monographs such as Indian Ocean (Fig. -
Austin, J.J. and Arnold, E.N. 2001. Ancient Mitochondrial DNA And
Downloaded from rspb.royalsocietypublishing.org on October 20, 2010 doi 10.1098/rspb.2001.1825 Ancient mitochondrial DNA and morphology elucidate an extinct island radiation of Indian Ocean giant tortoises (Cylindraspis) Jeremy J. Austin{ and E. Nicholas Arnold* Reptile Research Group, Department of Zoology,The Natural History Museum, Cromwell Road, London SW7 5BD, UK Ancient mitochondrial DNA sequences were used for investigating the evolution of an entire clade of extinct vertebrates, the endemic tortoises (Cylindraspis) of the Mascarene Islands in the Indian Ocean. Mitochondrial DNA corroborates morphological evidence that there were ¢ve species of tortoise with the following relationships: Cylindraspis triserrata ((Cylindraspis vosmaeri and Cylindraspis peltastes)(Cylindraspis inepta and Cylindraspis indica)).Phylogeny indicates that the ancestor of the group ¢rst colonized Mauritius where speciation produced C. triserrata and the ancestor of the other species including a second sympatric Mauritian form, C. inepta.A propagule derived from this lineage colonized Rodrigues 590 km to the east, where a second within-island speciation took place producing the sympatric C. vosmaeri and C. peltastes.A recent colonization of Re¨ union 150 km to the southwest produced C. indica.In the virtual absence of predators, the defensive features of the shells of Mascarene tortoises were largely dismantled, apparently in two stages.`Saddlebacked' shells with high fronts evolved independently on all three islands.This and other features, such as a derived jaw structure and small body size, may be associated with niche di¡eren- tiation in sympatric species and may represent a striking example of parallel di¡erentiation in a large terrestrial vertebrate.The history of Mascarene tortoises contrasts with that of the Gala¨ pagos, where only a single species is present and surviving populations are genetically much more similar.However, they too show some reduction in anti-predator mechanisms and multiple development of populations with saddlebacked shells. -
I Online Supplementary Data – Sexual Size Dimorphism in Salamanders
Online Supplementary data – Sexual size dimorphism in salamanders Supplementary data S1. Species data used in this study and references list. Males Females SSD Significant test Ref Species n SVL±SD n SVL±SD Andrias davidianus 2 532.5 8 383.0 -0.280 12 Cryptobranchus alleganiensis 53 277.4±5.2 52 300.9±3.4 0.084 Yes 61 Batrachuperus karlschmidti 10 80.0 10 84.8 0.060 26 Batrachuperus londongensis 20 98.6 10 96.7 -0.019 12 Batrachuperus pinchonii 5 69.6 5 74.6 0.070 26 Batrachuperus taibaiensis 11 92.9±12.1 9 102.1±7.1 0.099 Yes 27 Batrachuperus tibetanus 10 94.5 10 92.8 -0.017 12 Batrachuperus yenyuadensis 10 82.8 10 74.8 -0.096 26 Hynobius abei 24 57.8±2.1 34 55.0±1.2 -0.048 Yes 92 Hynobius amakusaensis 22 75.4±4.8 12 76.5±3.6 0.014 No 93 Hynobius arisanensis 72 54.3±4.8 40 55.2±4.8 0.016 No 94 Hynobius boulengeri 37 83.0±5.4 15 91.5±3.8 0.102 Yes 95 Hynobius formosanus 15 53.0±4.4 8 52.4±3.9 -0.011 No 94 Hynobius fuca 4 50.9±2.8 3 52.8±2.0 0.037 No 94 Hynobius glacialis 12 63.1±4.7 11 58.9±5.2 -0.066 No 94 Hynobius hidamontanus 39 47.7±1.0 15 51.3±1.2 0.075 Yes 96 Hynobius katoi 12 58.4±3.3 10 62.7±1.6 0.073 Yes 97 Hynobius kimurae 20 63.0±1.5 15 72.7±2.0 0.153 Yes 98 Hynobius leechii 70 61.6±4.5 18 66.5±5.9 0.079 Yes 99 Hynobius lichenatus 37 58.5±1.9 2 53.8 -0.080 100 Hynobius maoershanensis 4 86.1 2 80.1 -0.069 101 Hynobius naevius 72.1 76.7 0.063 102 Hynobius nebulosus 14 48.3±2.9 12 50.4±2.1 0.043 Yes 96 Hynobius osumiensis 9 68.4±3.1 15 70.2±3.0 0.026 No 103 Hynobius quelpaertensis 41 52.5±3.8 4 61.3±4.1 0.167 Yes 104 Hynobius -
Bonn Zoological Bulletin Volume 60 Issue 1 Pp
1 © Biodiversity Heritage Library, http://www.biodiversitylibrary.org/; www.zoologicalbulletin.de; www.biologiezentrum.at Bonn zoological Bulletin Volume 60 Issue 1 pp. 63-65 Bonn, May 201 A new record of the Persian Brook Salamander, Paradactylodon persicus (Eiselt & Steiner, 1970) (Amphibia: Caudata: Hynobiidae) in northern Iran 1 2 3 4 2 - Faraham Ahmadzadeh \ Fatemeh Khanjani , Aref Shadkam & Wolfgang Bohme 'Department of Biodiversity and Ecosystem Management, Environmental Sciences Research Institute, Shahid Beheshti University, Evin, Tehran, G. C, Iran 2 Herpetology Section, Zoologisches Forschungsmuseum Alexander Koenig (ZFMK), Adenauerallee 160, D-53113 Bonn, Germany 3 Department of Habitat and Biodiversity, Faculty of Environment and Energy, Science and Research Branch, Islamic Azad University, Ponak, Tehran, Iran 4 Department of Environment, Rezvan Shahr, Province Gilan, Iran "Corresponding Email address: [email protected]. INTRODUCTION The Persian Brook Salamander, Paradactylodon persicus 90 mm; tail length 120 mm; head large, 20 mm in length; (Eiselt & Steiner, 1970) is an endemic and poorly known vomerine teeth in two arch-shaped rows; snout rounded; species of northern Iran (Baloutch & Kami 1995; Kami fore and hind limbs with four digits; tail flattened later- 1999). It was originally described as Batrachuperus per- ally, with round-tapered end; dorsal head and body, as well sicus by Eiselt & Steiner ( 1 970), but has been transferred as upper surface of tail brownish with yellow spots and to the genus Paradactylodon based on genetic studies by marblings; belly cream without pattern (Fig. 2a-b). Zhang et al. (2006). This species has been reported from two localities only: Weyser, southeast of Chalus, in Paradactylodon persicus inhabits the mountainous Mazandaran Province (36° 30' 35" N and 51° 26' 38" E) streams and brooks, with cool, fast-flowing water and Delmadeh village, southeast of Khalkhal, in Ardabil (Baloutch & Kami 1995; Kami 1999; Ahmadzadeh & Ka- Province (37° 22' 34" N and 48° 47' 35" E) (Kami 2004; mi 2009). -
Environmental and Ecological Factors Affecting the Presence of Giant Land Turtles in the Late Cenozoic Author: Orion Jenkins-Hou
Environmental and Ecological Factors Affecting the Presence of Giant Land Turtles in the Late Cenozoic Author: Orion Jenkins-Houk GEOL394 Advisor: Dr. Thomas Holtz Due 4/28/2020 1 Abstract: Various species of turtles within Testudinidae (true tortoises) and the recently extinct Meiolaniidae of Australia grew to immense proportions throughout the late Cenozoic, including a significant number of taxa that have persisted into modern times. Although these giant land turtles mostly occur on islands today, there are cases of extinct giant land turtles on every non- Antarctic continent during the Cenozoic. This raises an interesting question: if giant turtles can occur on the continents, presumably in the presence of both predators capable of penetrating their defensive carapace and other herbivores competing for the same food sources, what other factors may be related to the evolution of gigantism in land turtles? This study tests the influence of two ecological factors, presence of durophagous (bone-crushing) predators and competing herbivores, and three environmental factors, mean annual temperature, aridity, and landmass type (insular versus continental) on occurrences of giant land turtles. The results of the Fisher exact tests collected demonstrate that the presence of competing herbivores and insularity have a significant effect on the occurrence of modern giant land turtles. Miocene giant land turtles appear to occur independently of all five factors, while Pliocene giants tend to occur in areas of higher average temperatures. Pleistocene