Animal Phylogeny and Its Evolutionary Implications∗
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University of Copenhagen, Zoological Museum, Review Universitetsparken 15, DK-2100 Copenhagen, Denmark CN, 0000-0001-6898-7655 Cite This Article: Nielsen C
Early animal evolution a morphologist's view Nielsen, Claus Published in: Royal Society Open Science DOI: 10.1098/rsos.190638 Publication date: 2019 Document version Publisher's PDF, also known as Version of record Document license: CC BY Citation for published version (APA): Nielsen, C. (2019). Early animal evolution: a morphologist's view. Royal Society Open Science, 6(7), 1-10. [190638]. https://doi.org/10.1098/rsos.190638 Download date: 30. sep.. 2021 Early animal evolution: a morphologist’s view royalsocietypublishing.org/journal/rsos Claus Nielsen The Natural History Museum of Denmark, University of Copenhagen, Zoological Museum, Review Universitetsparken 15, DK-2100 Copenhagen, Denmark CN, 0000-0001-6898-7655 Cite this article: Nielsen C. 2019 Early animal evolution: a morphologist’s view. R. Soc. open sci. Two hypotheses for the early radiation of the metazoans are vividly discussed in recent phylogenomic studies, the ‘Porifera- 6: 190638. first’ hypothesis, which places the poriferans as the sister group http://dx.doi.org/10.1098/rsos.190638 of all other metazoans, and the ‘Ctenophora-first’ hypothesis, which places the ctenophores as the sister group to all other metazoans. It has been suggested that an analysis of morphological characters (including specific molecules) could Received: 5 April 2019 throw additional light on the controversy, and this is the aim of Accepted: 4 July 2019 this paper. Both hypotheses imply independent evolution of nervous systems in Planulozoa and Ctenophora. The Porifera- first hypothesis implies no homoplasies or losses of major characters. The Ctenophora-first hypothesis shows no important synapomorphies of Porifera, Planulozoa and Placozoa. It implies Subject Category: either independent evolution, in Planulozoa and Ctenophora, of Biology (whole organism) a new digestive system with a gut with extracellular digestion, which enables feeding on larger organisms, or the subsequent Subject Areas: loss of this new gut in the Poriferans (and the re-evolution of the evolution collar complex). -
Placozoans Are Eumetazoans Related to Cnidaria
bioRxiv preprint doi: https://doi.org/10.1101/200972; this version posted October 11, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. 1 Placozoans are eumetazoans related to Cnidaria Christopher E. Laumer1,2, Harald Gruber-Vodicka3, Michael G. Hadfield4, Vicki B. Pearse5, Ana Riesgo6, 4 John C. Marioni1,2,7, and Gonzalo Giribet8 1. Wellcome Trust Sanger Institute, Hinxton, CB10 1SA, United Kingdom 2. European Molecular Biology Laboratories-European Bioinformatics Institute, Hinxton, CB10 1SD, United Kingdom 8 3. Max Planck Institute for Marine Microbiology, Celsiusstraβe 1, D-28359 Bremen, Germany 4. Kewalo Marine Laboratory, Pacific Biosciences Research Center/University of Hawaiʻi at Mānoa, 41 Ahui Street, Honolulu, HI 96813, United States of America 5. University of California, Santa Cruz, Institute of Marine Sciences, 1156 High Street, Santa 12 Cruz, CA 95064, United States of America 6. The Natural History Museum, Life Sciences, Invertebrate Division Cromwell Road, London SW7 5BD, United Kingdom 7. Cancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, 16 Robinson Way, Cambridge CB2 0RE, United Kingdom 8. Museum of Comparative Zoology, Department of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, United States of America 20 bioRxiv preprint doi: https://doi.org/10.1101/200972; this version posted October 11, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. -
The Evolution of Animal Genomes
Available online at www.sciencedirect.com ScienceDirect The evolution of animal genomes 1 2,3 Casey W Dunn and Joseph F Ryan Genome sequences are now available for hundreds of species We are still at a very early stage of the genomic revolution, sampled across the animal phylogeny, bringing key features of not unlike the state of computing in the late nineties [1]. animal genome evolution into sharper focus. The field of animal Genome sequences of various levels of quality are now evolutionary genomics has focused on identifying and available for a few hundred animal species thanks to the classifying the diversity genomic features, reconstructing the concerted efforts of large collaborative projects [2–4], more history of evolutionary changes in animal genomes, and testing recent efforts by smaller groups [5–7], and even genome hypotheses about the evolutionary relationships of animals. projects undertaken largely by independent laboratories The grand challenges moving forward are to connect [8,9]. At least 212 animal genomes have been published evolutionary changes in genomes with particular evolutionary (Figure 1) and many others are publicly available in various changes in phenotypes, and to determine which changes are stages of assembly and annotation. This sampling is still driven by selection. This will require far greater genome very biased towards animals with small genomes that can sampling both across and within species, extensive phenotype be bred in the laboratory and those from a small set of data, a well resolved animal phylogeny, and advances in phylogenetic clades. 83% of published genomes belong to comparative methods. vertebrates and arthropods (Figure 1). -
Animal Phylogeny and the Ancestry of Bilaterians: Inferences from Morphology and 18S Rdna Gene Sequences
EVOLUTION & DEVELOPMENT 3:3, 170–205 (2001) Animal phylogeny and the ancestry of bilaterians: inferences from morphology and 18S rDNA gene sequences Kevin J. Peterson and Douglas J. Eernisse* Department of Biological Sciences, Dartmouth College, Hanover NH 03755, USA; and *Department of Biological Science, California State University, Fullerton CA 92834-6850, USA *Author for correspondence (email: [email protected]) SUMMARY Insight into the origin and early evolution of the and protostomes, with ctenophores the bilaterian sister- animal phyla requires an understanding of how animal group, whereas 18S rDNA suggests that the root is within the groups are related to one another. Thus, we set out to explore Lophotrochozoa with acoel flatworms and gnathostomulids animal phylogeny by analyzing with maximum parsimony 138 as basal bilaterians, and with cnidarians the bilaterian sister- morphological characters from 40 metazoan groups, and 304 group. We suggest that this basal position of acoels and gna- 18S rDNA sequences, both separately and together. Both thostomulids is artifactal because for 1000 replicate phyloge- types of data agree that arthropods are not closely related to netic analyses with one random sequence as outgroup, the annelids: the former group with nematodes and other molting majority root with an acoel flatworm or gnathostomulid as the animals (Ecdysozoa), and the latter group with molluscs and basal ingroup lineage. When these problematic taxa are elim- other taxa with spiral cleavage. Furthermore, neither brachi- inated from the matrix, the combined analysis suggests that opods nor chaetognaths group with deuterostomes; brachiopods the root lies between the deuterostomes and protostomes, are allied with the molluscs and annelids (Lophotrochozoa), and Ctenophora is the bilaterian sister-group. -
Type Specimens of Gordioids (Nematoida: Nematomorpha) in the National Museum, Prague1
Journal of the National Museum (Prague), Natural History Series Vol. 181 (): ..-..; published on ... November 2012 ISSN 1802-6842 (print), 1802-6850 (electronic) Copyright © Národní muzeum, Praha, 2012 Type specimens of gordioids (Nematoida: Nematomorpha) in the National Museum, Prague1 Petr Dolejš Department of Zoology, National Museum, Cirkusová 1740, CZ-193 00 Praha 9 – Horní Počernice, Czech Republic; e-mail: [email protected] Abstract. The National Museum, Prague, Czech Republic, possesses type specimens of three species and one subspecies of horsehair worms: Gordionus formidatus Havlík, 1954 (Chordodidae), Gordionus scaber hykai Havlík, 1947 (Chordodidae), Gordius sinareolatus Havlík, 1949 (Gordiidae), and Paragordionus bohemicus Havlík, 1947 (Chordodidae). Key words: horsehair worms, Gordioida, type specimens, Otto Havlík, Czech Republic, Slovakia. INTRODUCTION Gordioids belongs to the phylum Nematomorpha (the so-called horsehair worms) which forms with the phylum Nematoda a monophyletic clade Nematoida (Schmidt-Rhaesa 1998) belonging to Ecdysozoa (Edgecombe et al. 2011). There are about 360 species of horsehair worms described so far (Schmidt-Rhaesa 2010). The most important part of the gordioid collection in the National Museum, Prague, Czech Republic (NMP) is the Havlík Collection, which contains all type specimens of gordioids possessed by the NMP; they are listed below. Dr. Otto Havlík (1923-1960; Fig. 1) was a renowned parasitologist, with special in- terest in gordioid systematics (Jírovec 1961). He described four new species and one new subspecies of gordioids (Havlík 1947, 1949c, 1954b) from specimens collected in the former Czechoslovakia (Bezděk 2011). All these taxa are currently considered valid (Schmidt-Rhaesa 2010, Bezděk 2011). In addition, he published the first description of a male of Gordius perronciti Camerano, 1887 (Havlík 1954b) and improved the descrip- tion of several more European species (Havlík 1949b). -
Ecdysozoan Phylogeny and Bayesian Inference: First Use of Nearly Complete 28S and 18S Rrna Gene Sequences to Classify the Arthro
MOLECULAR PHYLOGENETICS AND EVOLUTION Molecular Phylogenetics and Evolution 31 (2004) 178–191 www.elsevier.com/locate/ympev Ecdysozoan phylogeny and Bayesian inference: first use of nearly complete 28S and 18S rRNA gene sequences to classify the arthropods and their kinq Jon M. Mallatt,a,* James R. Garey,b and Jeffrey W. Shultzc a School of Biological Sciences, Washington State University, Pullman, WA 99164-4236, USA b Department of Biology, University of South Florida, 4202 East Fowler Ave. SCA110, Tampa, FL 33620, USA c Department of Entomology, University of Maryland, College Park, MD 20742, USA Received 4 March 2003; revised 18 July 2003 Abstract Relationships among the ecdysozoans, or molting animals, have been difficult to resolve. Here, we use nearly complete 28S + 18S ribosomal RNA gene sequences to estimate the relations of 35 ecdysozoan taxa, including newly obtained 28S sequences from 25 of these. The tree-building algorithms were likelihood-based Bayesian inference and minimum-evolution analysis of LogDet-trans- formed distances, and hypotheses were tested wth parametric bootstrapping. Better taxonomic resolution and recovery of estab- lished taxa were obtained here, especially with Bayesian inference, than in previous parsimony-based studies that used 18S rRNA sequences (or 18S plus small parts of 28S). In our gene trees, priapulan worms represent the basal ecdysozoans, followed by ne- matomorphs, or nematomorphs plus nematodes, followed by Panarthropoda. Panarthropoda was monophyletic with high support, although the relationships among its three phyla (arthropods, onychophorans, tardigrades) remain uncertain. The four groups of arthropods—hexapods (insects and related forms), crustaceans, chelicerates (spiders, scorpions, horseshoe crabs), and myriapods (centipedes, millipedes, and relatives)—formed two well-supported clades: Hexapoda in a paraphyletic crustacea (Pancrustacea), and ÔChelicerata + MyriapodaÕ (a clade that we name ÔParadoxopodaÕ). -
Reconstruction of the Ancestral Metazoan Genome Reveals an Increase in Genomic Novelty
Paps, J. , & Holland, P. W. H. (2018). Reconstruction of the ancestral metazoan genome reveals an increase in genomic novelty. Nature Communications, 9, [1730]. https://doi.org/10.1038/s41467-018- 04136-5 Publisher's PDF, also known as Version of record License (if available): CC BY Link to published version (if available): 10.1038/s41467-018-04136-5 Link to publication record in Explore Bristol Research PDF-document This is the final published version of the article (version of record). It first appeared online via Nature Research at https://www.nature.com/articles/s41467-018-04136-5#article-info . Please refer to any applicable terms of use of the publisher. University of Bristol - Explore Bristol Research General rights This document is made available in accordance with publisher policies. Please cite only the published version using the reference above. Full terms of use are available: http://www.bristol.ac.uk/red/research-policy/pure/user-guides/ebr-terms/ ARTICLE DOI: 10.1038/s41467-018-04136-5 OPEN Reconstruction of the ancestral metazoan genome reveals an increase in genomic novelty Jordi Paps1,2 & Peter W.H. Holland 2 Understanding the emergence of the Animal Kingdom is one of the major challenges of modern evolutionary biology. Many genomic changes took place along the evolutionary lineage that gave rise to the Metazoa. Recent research has revealed the role that co-option of 1234567890():,; old genes played during this transition, but the contribution of genomic novelty has not been fully assessed. Here, using extensive genome comparisons between metazoans and multiple outgroups, we infer the minimal protein-coding genome of the first animal, in addition to other eukaryotic ancestors, and estimate the proportion of novelties in these ancient gen- omes. -
Introduction to the Bilateria and the Phylum Xenacoelomorpha Triploblasty and Bilateral Symmetry Provide New Avenues for Animal Radiation
CHAPTER 9 Introduction to the Bilateria and the Phylum Xenacoelomorpha Triploblasty and Bilateral Symmetry Provide New Avenues for Animal Radiation long the evolutionary path from prokaryotes to modern animals, three key innovations led to greatly expanded biological diversification: (1) the evolution of the eukaryote condition, (2) the emergence of the A Metazoa, and (3) the evolution of a third germ layer (triploblasty) and, perhaps simultaneously, bilateral symmetry. We have already discussed the origins of the Eukaryota and the Metazoa, in Chapters 1 and 6, and elsewhere. The invention of a third (middle) germ layer, the true mesoderm, and evolution of a bilateral body plan, opened up vast new avenues for evolutionary expan- sion among animals. We discussed the embryological nature of true mesoderm in Chapter 5, where we learned that the evolution of this inner body layer fa- cilitated greater specialization in tissue formation, including highly specialized organ systems and condensed nervous systems (e.g., central nervous systems). In addition to derivatives of ectoderm (skin and nervous system) and endoderm (gut and its de- Classification of The Animal rivatives), triploblastic animals have mesoder- Kingdom (Metazoa) mal derivatives—which include musculature, the circulatory system, the excretory system, Non-Bilateria* Lophophorata and the somatic portions of the gonads. Bilater- (a.k.a. the diploblasts) PHYLUM PHORONIDA al symmetry gives these animals two axes of po- PHYLUM PORIFERA PHYLUM BRYOZOA larity (anteroposterior and dorsoventral) along PHYLUM PLACOZOA PHYLUM BRACHIOPODA a single body plane that divides the body into PHYLUM CNIDARIA ECDYSOZOA two symmetrically opposed parts—the left and PHYLUM CTENOPHORA Nematoida PHYLUM NEMATODA right sides. -
Placozoans Are Eumetazoans Related to Cnidaria
bioRxiv preprint first posted online Oct. 11, 2017; doi: http://dx.doi.org/10.1101/200972. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC 4.0 International license. 1 Placozoans are eumetazoans related to Cnidaria Christopher E. Laumer1,2, Harald Gruber-Vodicka3, Michael G. Hadfield4, Vicki B. Pearse5, Ana Riesgo6, 4 John C. Marioni1,2,7, and Gonzalo Giribet8 1. Wellcome Trust Sanger Institute, Hinxton, CB10 1SA, United Kingdom 2. European Molecular Biology Laboratories-European Bioinformatics Institute, Hinxton, CB10 1SD, United Kingdom 8 3. Max Planck Institute for Marine Microbiology, Celsiusstraβe 1, D-28359 Bremen, Germany 4. Kewalo Marine Laboratory, Pacific Biosciences Research Center/University of Hawaiʻi at Mānoa, 41 Ahui Street, Honolulu, HI 96813, United States of America 5. University of California, Santa Cruz, Institute of Marine Sciences, 1156 High Street, Santa 12 Cruz, CA 95064, United States of America 6. The Natural History Museum, Life Sciences, Invertebrate Division Cromwell Road, London SW7 5BD, United Kingdom 7. Cancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, 16 Robinson Way, Cambridge CB2 0RE, United Kingdom 8. Museum of Comparative Zoology, Department of Organismic and Evolutionary Biology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, United States of America 20 bioRxiv preprint first posted online Oct. 11, 2017; doi: http://dx.doi.org/10.1101/200972. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC 4.0 International license. -
OEB51: the Biology and Evolu on of Invertebrate Animals
OEB51: The Biology and Evoluon of Invertebrate Animals Lectures: BioLabs 2062 Labs: BioLabs 5088 Instructor: Cassandra Extavour BioLabs 4103 (un:l Feb. 11) BioLabs2087 (aer Feb. 11) 617 496 1935 [email protected] Teaching Assistant: Tauana Cunha MCZ Labs 5th Floor [email protected] Basic Info about OEB 51 • Lecture Structure: • Tuesdays 1-2:30 Pm: • ≈ 1 hour lecture • ≈ 30 minutes “Tech Talk” • the lecturer will explain some of the key techniques used in the primary literature paper we will be discussing that week • Wednesdays: • By the end of lab (6pm), submit at least one quesBon(s) for discussion of the primary literature paper for that week • Thursdays 1-2:30 Pm: • ≈ 1 hour lecture • ≈ 30 minutes Paper discussion • Either the lecturer or teams of 2 students will lead the class in a discussion of the primary literature paper for that week • There Will be a total of 7 Paper discussions led by students • On Thursday January 28, We Will have the list of Papers to be discussed, and teams can sign uP to Present Basic Info about OEB 51 • Bocas del Toro, Panama Field Trip: • Saturday March 12 to Sunday March 20, 2016: • This field triP takes Place during sPring break! • It is mandatory to aend the field triP but… • …OEB51 Will not meet during the Week folloWing the field triP • Saturday March 12: • fly to Panama City, stay there overnight • Sunday March 13: • fly to Bocas del Toro, head out for our first collec:on! • Monday March 14 – Saturday March 19: • breakfast, field collec:ng (lunch on the boat), animal care at sea tables, -
The Evolution of Metazoan Axial Properties
FOCUS ON THE BODY PLAN THE EVOLUTION OF METAZOAN AXIAL PROPERTIES Mark Q. Martindale Abstract | Renewed interest in the developmental basis of organismal complexity, and the emergence of new molecular tools, is improving our ability to study the evolution of metazoan body plans. The most substantial changes in body-plan organization occurred early in metazoan evolution; new model systems for studying basal metazoans are now being developed, and total-genome-sequencing initiatives are underway for at least three of the four most important taxa. The elucidation of how the gene networks that are involved in axial organization, germ-layer formation and cell differentiation are used differently during development is generating a more detailed understanding of the events that have led to the current diversity of multicellular life. METAZOAN Some of the most fundamental unanswered questions the proteins decapentaplegic or bone morphogenetic A multicellular animal. in biology revolve around the origin and tremen- protein (Dpp/Bmp) and short gastrulation or chordin dous diversification of the multicellular animals that (Sog/Chrd) is shared by animals that are as distantly RADIAL SYMMETRY inhabited the Earth’s oceans more than 500 million related as vertebrates and flies5–8. The presence of multiple planes of mirror symmetry running years ago. Despite the great variation in form and Although there is no shortage of alternative theories through the longitudinal axis. function of METAZOANS the body plan of most of these (see REF. 9 for an historical review), bilaterally sym- species is organized along a single longitudinal axis, the metrical animals are thought to have evolved from GASTRULATION anterior–posterior axis (A–P axis). -
Ecdysozoan Phylogeny and Bayesian Inference: first Use of Nearly Complete 28S and 18S Rrna Gene Sequences to Classify the Arthropods and Their Kinq
ARTICLE IN PRESS MOLECULAR PHYLOGENETICS AND EVOLUTION Molecular Phylogenetics and Evolution xxx (2003) xxx–xxx www.elsevier.com/locate/ympev Ecdysozoan phylogeny and Bayesian inference: first use of nearly complete 28S and 18S rRNA gene sequences to classify the arthropods and their kinq Jon M. Mallatt,a,* James R. Garey,b and Jeffrey W. Shultzc a School of Biological Sciences, Washington State University, Pullman, WA 99164-4236, USA b Department of Biology, University of South Florida, 4202 East Fowler Ave. SCA110, Tampa, FL 33620, USA c Department of Entomology, University of Maryland, College Park, MD 20742, USA Received 4 March 2003; revised 18 July 2003 Abstract Relationships among the ecdysozoans, or molting animals, have been difficult to resolve. Here, we use nearly complete 28S + 18S ribosomal RNA gene sequences to estimate the relations of 35 ecdysozoan taxa, including newly obtained 28S sequences from 25 of these. The tree-building algorithms were likelihood-based Bayesian inference and minimum-evolution analysis of LogDet-trans- formed distances, and hypotheses were tested wth parametric bootstrapping. Better taxonomic resolution and recovery of estab- lished taxa were obtained here, especially with Bayesian inference, than in previous parsimony-based studies that used 18S rRNA sequences (or 18S plus small parts of 28S). In our gene trees, priapulan worms represent the basal ecdysozoans, followed by ne- matomorphs, or nematomorphs plus nematodes, followed by Panarthropoda. Panarthropoda was monophyletic with high support, although the relationships among its three phyla (arthropods, onychophorans, tardigrades) remain uncertain. The four groups of arthropods—hexapods (insects and related forms), crustaceans, chelicerates (spiders, scorpions, horseshoe crabs), and myriapods (centipedes, millipedes, and relatives)—formed two well-supported clades: Hexapoda in a paraphyletic crustacea (Pancrustacea), and ÔChelicerata + MyriapodaÕ (a clade that we name ÔParadoxopodaÕ).