Phyla Echinodermata and Chordata Deuterostomes!
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Flatworms Phylum Platyhelminthes
Flatworms Phylum Platyhelminthes The flatworms include more than 13,000 species of free-living and parasitic species.There are 3 classes of flat- worms, the planarians, flukes and tapeworms. General Physical Traits (Anatomy): Flatworms are bilaterally symmetrical. This means that they can only be cut them length-wise to produce two mirror-image halves. They have a distinct right and left half. This is differ- ent from radially symmetrical animals, like the anemones, which can be cut anywhere top to bottom to get two similar halves. Flatworms have 3 tissue layers, compared to the 2 layers in sponges and cnidarians (jellyfishes, anemones and corals). They also have only one opening for food to enter and waste to leave, like the sponges and cnidarians. This is called a “sac” body plan. Planarian (class Tubellaria) Habitat: They live mostly in saltwater (marine) habitats, but are also found in freshwater. Habits: They are free-living flatworms (not parasites). Physical Traits (Anatomy): Planarians are small - less than a centimeter long. They have a head, brain and sense organs. This is called “cephalization.” The sense organs – called eyespots – look like eyes and are sensitive to light changes, but are not like human eyes. They are made up of simple nerve cells that respond to stimuli, like light. When many nerve cells are gathered in one place, they are called a “ganglion,” so the two eyespots are actually ganglia. They also have points on either side of the head that look a bit like ears, called “sensory lobes” or auricles. They do not hear, but can sense food. -
The Phylum Vertebrata: a Case for Zoological Recognition Naoki Irie1,2* , Noriyuki Satoh3 and Shigeru Kuratani4
Irie et al. Zoological Letters (2018) 4:32 https://doi.org/10.1186/s40851-018-0114-y REVIEW Open Access The phylum Vertebrata: a case for zoological recognition Naoki Irie1,2* , Noriyuki Satoh3 and Shigeru Kuratani4 Abstract The group Vertebrata is currently placed as a subphylum in the phylum Chordata, together with two other subphyla, Cephalochordata (lancelets) and Urochordata (ascidians). The past three decades, have seen extraordinary advances in zoological taxonomy and the time is now ripe for reassessing whether the subphylum position is truly appropriate for vertebrates, particularly in light of recent advances in molecular phylogeny, comparative genomics, and evolutionary developmental biology. Four lines of current research are discussed here. First, molecular phylogeny has demonstrated that Deuterostomia comprises Ambulacraria (Echinodermata and Hemichordata) and Chordata (Cephalochordata, Urochordata, and Vertebrata), each clade being recognized as a mutually comparable phylum. Second, comparative genomic studies show that vertebrates alone have experienced two rounds of whole-genome duplication, which makes the composition of their gene family unique. Third, comparative gene-expression profiling of vertebrate embryos favors an hourglass pattern of development, the most conserved stage of which is recognized as a phylotypic period characterized by the establishment of a body plan definitively associated with a phylum. This mid-embryonic conservation is supported robustly in vertebrates, but only weakly in chordates. Fourth, certain complex patterns of body plan formation (especially of the head, pharynx, and somites) are recognized throughout the vertebrates, but not in any other animal groups. For these reasons, we suggest that it is more appropriate to recognize vertebrates as an independent phylum, not as a subphylum of the phylum Chordata. -
"Lophophorates" Brachiopoda Echinodermata Asterozoa
Deuterostomes Bryozoa Phoronida "lophophorates" Brachiopoda Echinodermata Asterozoa Stelleroidea Asteroidea Ophiuroidea Echinozoa Holothuroidea Echinoidea Crinozoa Crinoidea Chaetognatha (arrow worms) Hemichordata (acorn worms) Chordata Urochordata (sea squirt) Cephalochordata (amphioxoius) Vertebrata PHYLUM CHAETOGNATHA (70 spp) Arrow worms Fossils from the Cambrium Carnivorous - link between small phytoplankton and larger zooplankton (1-15 cm long) Pharyngeal gill pores No notochord Peculiar origin for mesoderm (not strictly enterocoelous) Uncertain relationship with echinoderms PHYLUM HEMICHORDATA (120 spp) Acorn worms Pharyngeal gill pores No notochord (Stomochord cartilaginous and once thought homologous w/notochord) Tornaria larvae very similar to asteroidea Bipinnaria larvae CLASS ENTEROPNEUSTA (acorn worms) Marine, bottom dwellers CLASS PTEROBRANCHIA Colonial, sessile, filter feeding, tube dwellers Small (1-2 mm), "U" shaped gut, no gill slits PHYLUM CHORDATA Body segmented Axial notochord Dorsal hollow nerve chord Paired gill slits Post anal tail SUBPHYLUM UROCHORDATA Marine, sessile Body covered in a cellulose tunic ("Tunicates") Filter feeder (» 200 L/day) - perforated pharnx adapted for filtering & repiration Pharyngeal basket contractable - squirts water when exposed at low tide Hermaphrodites Tadpole larvae w/chordate characteristics (neoteny) CLASS ASCIDIACEA (sea squirt/tunicate - sessile) No excretory system Open circulatory system (can reverse blood flow) Endostyle - (homologous to thyroid of vertebrates) ciliated groove -
Przedstawiciele Rodzaju Craniscus Dali, 1871 Z Górnego Oksfordu Bielaw I Wapienna Na Kujawach
Przedstawic iele rodza ju Craniscus Da li. 187 1 z górnego oksfordu Bielaw i Wapienna na Kujawach 75 Przedstawiciele rodzaju Craniscus Dali, 1871 z górnego oksfordu Bielaw i Wapienna na Kujawach Representatives of the genus Craniscus Dali, 1871, from the Upper Oxfordian of Bielawy and Wapienno in Kujawy area Cezary KRAWCZYŃSKI Instytut Geologii Pod stawowej. Wydziat Geologii. Un iwers ytet Warszawski. ul. Ż wirk i i Wigury 93. 02-089 Warszaw a; e-mail : c.kra [email protected] Key words: Craniidae, Craniscus, Inarticulated Brachiopods, Upper Jurassic, Poland. ABSTRACT: The presented paper contains a detailed description of four species of the genus Craniscus DalI, 1871, found in the Upper Oxfordian of Bielawy and Wapienno quarries, Kujawy area. Three of them: Craniscus bipartitus (Munster, 1837), Craniscus antiquior (Jelly, 1843) and Craniscus corallinus (Quenstedt, 1852) have already been described from Poland, the fourth, however - Craniscus tripartitus (Munster, 1840) , had only been known from the Lower Oxfordian of North Bavaria. The Craniscus specimens come from slope deposits of sponge-microbialitic bioherm. This is indicated by the fact that almost all specimens are dorsal valves, separated posthumously from ventral valves. The condition of some specimens and the rock lithology suggests, that the deposition was very violent in some cases and brachiopods were buried alive. The studied material is relatively well-preserved, which alIowes an accurate reading of the location of muscle scal's. WSTĘP BUDOWA GEOLOGICZNA I STRATYGRAFIA Praca niniejsza zawiera opis czterech gatunków W kamieniołomach Wapienno i Bielawy eksplo kranii z rodzaju Craniscus Dall, 1871, znalezionych atowane są wapienie biohermy gąbkowo-mikrobial w osadach górnego oksfordu odsłoniętych w kamie itowej oraz jej skłonu, które stanowią fragment niołomach Wapienno i Bielawy (fig. -
Evidence for Selection on a Chordate Histocompatibility Locus
ORIGINAL ARTICLE doi:10.1111/j.1558-5646.2012.01787.x EVIDENCE FOR SELECTION ON A CHORDATE HISTOCOMPATIBILITY LOCUS Marie L. Nydam,1,2,3 Alyssa A. Taylor,3 and Anthony W. De Tomaso3 1Division of Science and Mathematics, Centre College, Danville, Kentucky 40422 2E-mail: [email protected] 3Department of Molecular, Cellular, and Developmental Biology, University of California Santa Barbara, Santa Barbara, California 93106 Received June 7, 2011 Accepted July 31, 2012 Allorecognition is the ability of an organism to differentiate self or close relatives from unrelated individuals. The best known applications of allorecognition are the prevention of inbreeding in hermaphroditic species (e.g., the self-incompatibility [SI] systems in plants), the vertebrate immune response to foreign antigens mediated by MHC loci, and somatic fusion, where two genetically independent individuals physically join to become a chimera. In the few model systems where the loci governing allorecognition outcomes have been identified, the corresponding proteins have exhibited exceptional polymorphism. But information about the evolution of this polymorphism outside MHC is limited. We address this subject in the ascidian Botryllus schlosseri,where allorecognition outcomes are determined by a single locus, called FuHC (Fusion/HistoCompatibility). Molecular variation in FuHC is distributed almost entirely within populations, with very little evidence for differentiation among different populations. Mutation plays a larger role than recombination in the creation of FuHC polymorphism. A selection statistic, neutrality tests, and distribution of variation within and among different populations all provide evidence for selection acting on FuHC, but are not in agreement as to whether the selection is balancing or directional. -
The Origins of Chordate Larvae Donald I Williamson* Marine Biology, University of Liverpool, Liverpool L69 7ZB, United Kingdom
lopmen ve ta e l B Williamson, Cell Dev Biol 2012, 1:1 D io & l l o l g DOI: 10.4172/2168-9296.1000101 e y C Cell & Developmental Biology ISSN: 2168-9296 Research Article Open Access The Origins of Chordate Larvae Donald I Williamson* Marine Biology, University of Liverpool, Liverpool L69 7ZB, United Kingdom Abstract The larval transfer hypothesis states that larvae originated as adults in other taxa and their genomes were transferred by hybridization. It contests the view that larvae and corresponding adults evolved from common ancestors. The present paper reviews the life histories of chordates, and it interprets them in terms of the larval transfer hypothesis. It is the first paper to apply the hypothesis to craniates. I claim that the larvae of tunicates were acquired from adult larvaceans, the larvae of lampreys from adult cephalochordates, the larvae of lungfishes from adult craniate tadpoles, and the larvae of ray-finned fishes from other ray-finned fishes in different families. The occurrence of larvae in some fishes and their absence in others is correlated with reproductive behavior. Adult amphibians evolved from adult fishes, but larval amphibians did not evolve from either adult or larval fishes. I submit that [1] early amphibians had no larvae and that several families of urodeles and one subfamily of anurans have retained direct development, [2] the tadpole larvae of anurans and urodeles were acquired separately from different Mesozoic adult tadpoles, and [3] the post-tadpole larvae of salamanders were acquired from adults of other urodeles. Reptiles, birds and mammals probably evolved from amphibians that never acquired larvae. -
Animal Origins and the Evolution of Body Plans 621
Animal Origins and the Evolution 32 of Body Plans In 1822, nearly forty years before Darwin wrote The Origin of Species, a French naturalist, Étienne Geoffroy Saint-Hilaire, was examining a lob- ster. He noticed that when he turned the lobster upside down and viewed it with its ventral surface up, its central nervous system was located above its digestive tract, which in turn was located above its heart—the same relative positions these systems have in mammals when viewed dorsally. His observations led Geoffroy to conclude that the differences between arthropods (such as lobsters) and vertebrates (such as mammals) could be explained if the embryos of one of those groups were inverted during development. Geoffroy’s suggestion was regarded as preposterous at the time and was largely dismissed until recently. However, the discovery of two genes that influence a sys- tem of extracellular signals involved in development has lent new support to Geof- froy’s seemingly outrageous hypothesis. Genes that Control Development A A vertebrate gene called chordin helps to establish cells on one side of the embryo human and a lobster carry similar genes that control the development of the body as dorsal and on the other as ventral. A probably homologous gene in fruit flies, called axis, but these genes position their body sog, acts in a similar manner, but has the opposite effect. Fly cells where sog is active systems inversely. A lobster’s nervous sys- become ventral, whereas vertebrate cells where chordin is active become dorsal. How- tem runs up its ventral (belly) surface, whereas a vertebrate’s runs down its dorsal ever, when sog mRNA is injected into an embryo (back) surface. -
Phylum Echinodermata Phylum Echinodermata
Phylum Echinodermata Phylum Echinodermata About 7,000 species Strictly marine, mostly benthic. Typical deuterostomes. Phylum Echinodermata Class Crinoidea (sea lilies) Phylum Echinodermata Class Crinoidea Class Asteroidea (sea stars) Phylum Echinodermata Class Crinoidea Class Asteroidea Class Ophiuroidea (brittle stars and basket stars) Phylum Echinodermata Class Crinoidea Class Asteroidea Class Ophiuroidea Class Echinoidea (sea urchins and sand dollars) Phylum Echinodermata Class Crinoidea Class Asteroidea Class Ophiuroidea Class Echinoidea Class Holothuroidea (sea cucumbers) What do Echinoderms look like? Pentamerous radial symmetry. Oral and aboral surfaces. Oral surface has ambulacral grooves associated with tubefeet called podia. What do Echinoderms look like? Oral and aboral surfaces. What do Echinoderms look like? Arms (ambulacra) numbered with reference to the madreporite. Ambulacrum opposite is A then proceed couterclockwise. Ambulara C and D are the bivium, A B and E are the trivium. What do Echinoderms look like? Body wall Epidermis covers entire body. Endoskeleton of ossicles with tubefeet and dermal branchia protruding through and spines and pedicellaria on outside. What do Echinoderms look like? Body wall Ossicles can be fused into a test (urchins and sand dollars). Ossicles spread apart in cucumbers. Ossicles intermediate and variable in seastars. Muscle fibers beneath ossicles. What do Echinoderms look like? Body wall Tubercles and moveable spines on skeletal plates of echinoids. Small muscles attach spines to test. What do Echinoderms look like? Water vascular system Fluid-filled canals for internal transport and locomotion. Fluid similar to sewater but has coelomcytes and organic molecules. Moved through system with cilia. What do Echinoderms look like? Water vascular system Asteroidea: Madreporite on aboral surface. -
Treatise on Invertebrate Paleontology
PART H, Revised BRACHIOPODA VOLUMES 2 & 3: Linguliformea, Craniiformea, and Rhynchonelliformea (part) ALWYN WILLIAMS, S. J. CARLSON, C. H. C. BRUNTON, L. E. HOLMER, L. E. POPOV, MICHAL MERGL, J. R. LAURIE, M. G. BASSETT, L. R. M. COCKS, RONG JIA-YU, S. S. LAZAREV, R. E. GRANT, P. R. RACHEBOEUF, JIN YU-GAN, B. R. WARDLAW, D. A. T. HARPER, A. D. WRIGHT, and MADIS RUBEL CONTENTS INFORMATION ON TREATISE VOLUMES ...................................................................................... x EDITORIAL PREFACE .............................................................................................................. xi STRATIGRAPHIC DIVISIONS .................................................................................................. xxiv COORDINATING AUTHOR'S PREFACE (Alwyn Williams) ........................................................ xxv BRACHIOPOD CLASSIFICATION (Alwyn Williams, Sandra J. Carlson, and C. Howard C. Brunton) .................................. 1 Historical Review .............................................................................................................. 1 Basis for Classification ....................................................................................................... 5 Methods.......................................................................................................................... 5 Genealogies ....................................................................................................................... 6 Recent Brachiopods ....................................................................................................... -
Phylum Chordata
Phylum Chordata 48,000 species very diverse phylum but still more unity in major characteristics than in most other phyla most advanced phylum of animal kingdom one to which we belong along with fish, amphibians reptiles, birds and other mammals some of the largest or most massive animals true coelom 4 major identifying characteristics: 1. Notochord flexible rodlike structure enclosed by a fibrous sheath extends the length of the body in larva and/or adult provides basic support and serves as main axis for muscle attachments to permit “fishlike” undulatory movements first part of skeleton to form in embryo in primitive chordates the notochord persists through life Animals: Chordates & Introduction to Vertebrates; Ziser Lecture Notes, 2006 1 in most chordates the notochord is replaced by a vertebral column of bone remnants of the notochord remain as “intervertebral discs” 2. Dorsal tubular nerve cord in most invert groups; nerve cord is ventral & paired in chordates the nerve cord is a single dorsal hollow nerve cord front end usually enlarged to form brain 3. Pharyngeal (gill) slits slit-like opening sleading from throat to outside first evolved as a filter feeding apparatus still used by some to filter water for food in others as gills in some groups they are only found in embryo and lost as adults 4. endostyle or thyroid gland specific kind of tissue found only in chordates was originally part of the feeding apparatus endostyle secretes mucus and traps food inside the pharyngeal cavity eg. lamprey larva in most chordates the same tissue has become an endocrine Animals: Chordates & Introduction to Vertebrates; Ziser Lecture Notes, 2006 2 gland in the neck region that helps control metabolism 5. -
Tropical Marine Invertebrates CAS BI 569 Phylum Echinodermata by J
Tropical Marine Invertebrates CAS BI 569 Phylum Echinodermata by J. R. Finnerty Porifera Ctenophora Cnidaria Deuterostomia Ecdysozoa Lophotrochozoa Chordata Arthropoda Annelida Hemichordata Onychophora Mollusca Echinodermata *Nematoda *Platyhelminthes Acoelomorpha Calcispongia Silicispongiae PROTOSTOMIA Phylum Phylum Phylum CHORDATA ECHINODERMATA HEMICHORDATA Blastopore -> anus Radial / equal cleavage Coelom forms by enterocoely ! Protostome = blastopore contributes to the mouth blastopore mouth anus ! Deuterostome = blastopore becomes anus blastopore anus mouth Halocynthia, a tunicate (Urochordata) Coelom Formation Protostomes: Schizocoely Deuterostomes: Enterocoely Enterocoely in a sea star Axocoel (protocoel) Gives rise to small portion of water vascular system. Hydrocoel (mesocoel) Gives rise to water vascular system. Somatocoel (metacoel) Gives rise to lining of adult body cavity. Echinoderm Metamorphosis ECHINODERM FEATURES Water vascular system and tube feet Pentaradial symmetry Coelom formation by enterocoely Water Vascular System Tube Foot Tube Foot Locomotion ECHINODERM DIVERSITY Crinoidea Asteroidea Ophiuroidea Holothuroidea Echinoidea “sea lilies” “sea stars” “brittle stars” “sea cucumbers” “urchins, sand dollars” Group Form & Habit Habitat Ossicles Feeding Special Characteristics Crinoids 5-200 arms, stalked epifaunal Internal skeleton suspension mouth upward; mucous & Of each arm feeders secreting glands on sessile podia Ophiuroids usually 5 thin arms, epifaunal ossicles in arms deposit feeders act and appear like vertebrae -
Development of the Annelid Axochord: Insights Into Notochord Evolution Antonella Lauri Et Al
RESEARCH | REPORTS ORIGIN OF NOTOCHORD by double WMISH (Fig. 2, F to L). Although none of the genes were exclusively expressed in the annelid mesodermal midline, their combined Development of the annelid coexpression was unique to these cells (implying that mesodermal midline in annelids and chor- damesoderm in vertebrates are more similar to axochord: Insights into each other than to any other tissue). It is unlikely that the molecular similarity between annelid notochord evolution and vertebrate mesodermal midline is due to in- dependent co-option of a conserved gene cas- Antonella Lauri,1*† Thibaut Brunet,1* Mette Handberg-Thorsager,1,2‡ sette, because this would require either that this Antje H.L. Fischer,1§ Oleg Simakov,1 Patrick R. H. Steinmetz,1‖ Raju Tomer,1,2¶ cassette was active elsewhere in the body (which Philipp J. Keller,2 Detlev Arendt1,3# is not the case) or that multiple identical inde- pendent events of co-option occurred (which is The origin of chordates has been debated for more than a century, with one key issue being unparsimonious). As in vertebrates, the meso- the emergence of the notochord. In vertebrates, the notochord develops by convergence dermal midline resembles the neuroectodermal and extension of the chordamesoderm, a population of midline cells of unique molecular midline, which expresses foxD, foxA, netrin, slit, identity. We identify a population of mesodermal cells in a developing invertebrate, the marine and noggin (figs. S6 and S7) but not brachyury or annelid Platynereis dumerilii, that converges and extends toward the midline and expresses a twist. However, unlike in chicken (10), the an- notochord-specific combination of genes.