Vertebrate Origins
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PALEONTOLOGICAL TECHNICAL REPORT: 6Th AVENUE and WADSWORTH BOULEVARD INTERCHANGE PHASE II ENVIRONMENTAL ASSESSMENT, CITY of LAKEWOOD, JEFFERSON COUNTY, COLORADO
PALEONTOLOGICAL TECHNICAL REPORT: 6th AVENUE AND WADSWORTH BOULEVARD INTERCHANGE PHASE II ENVIRONMENTAL ASSESSMENT, CITY OF LAKEWOOD, JEFFERSON COUNTY, COLORADO Prepared for: TEC Inc. 1746 Cole Boulevard, Suite 265 Golden, CO 80401 Prepared by: Paul C. Murphey, Ph.D. and David Daitch M.S. Rocky Mountain Paleontology 4614 Lonespur Court Oceanside, CA 92056 303-514-1095; 760-758-4019 www.rockymountainpaleontology.com Prepared under State of Colorado Paleontological Permit 2007-33 January, 2007 TABLE OF CONTENTS 1.0 SUMMARY............................................................................................................................. 3 2.0 INTRODUCTION ................................................................................................................... 4 2.1 DEFINITION AND SIGNIFICANCE OF PALEONTOLOGICAL RESOURCES........... 4 3.0 METHODS .............................................................................................................................. 6 4.0. LAWS, ORDINANCES, REGULATIONS AND STANDARDS......................................... 7 4.1. Federal................................................................................................................................. 7 4.2. State..................................................................................................................................... 8 4.3. County................................................................................................................................. 8 4.4. City..................................................................................................................................... -
Phylum Arthropod Silvia Rondon, and Mary Corp, OSU Extension Entomologist and Agronomist, Respectively Hermiston Research and Extension Center, Hermiston, Oregon
Phylum Arthropod Silvia Rondon, and Mary Corp, OSU Extension Entomologist and Agronomist, respectively Hermiston Research and Extension Center, Hermiston, Oregon Member of the Phyllum Arthropoda can be found in the seas, in fresh water, on land, or even flying freely; a group with amazing differences of structure, and so abundant that all the other animals taken together are less than 1/6 as many as the arthropods. Well-known members of this group are the Kingdom lobsters, crayfish and crabs; scorpions, spiders, mites, ticks, Phylum Phylum Phylum Class the centipedes and millipedes; and last, but not least, the Order most abundant of all, the insects. Family Genus The Phylum Arthropods consist of the following Species classes: arachnids, chilopods, diplopods, crustaceans and hexapods (insects). All arthropods possess: • Exoskeleton. A hard protective covering around the outside of the body (divided by sutures into plates called sclerites). An insect's exoskeleton (integument) serves as a protective covering over the body, but also as a surface for muscle attachment, a water-tight barrier against desiccation, and a sensory interface with the environment. It is a multi-layered structure with four functional regions: epicuticle (top layer), procuticle, epidermis, and basement membrane. • Segmented body • Jointed limbs and jointed mouthparts that allow extensive specialization • Bilateral symmetry, whereby a central line can divide the body Insect molting or removing its into two identical halves, left and right exoesqueleton • Ventral nerve -
The Metamorphosis of the Endostyle (Thy- Roid Gland) of Ammocoetes Branchialis (Larval Land-Locked Petromyzon Marinus (Jordan) Or Petromy- Zon Dorsatus (Wilder) ).*I
THE METAMORPHOSIS OF THE ENDOSTYLE (THY- ROID GLAND) OF AMMOCOETES BRANCHIALIS (LARVAL LAND-LOCKED PETROMYZON MARINUS (JORDAN) OR PETROMY- ZON DORSATUS (WILDER) ).*I BY DAVID MARINE, M.D. (From the H. K. Cushing Laboratory of Experimental Medicine, Western Reserve University, Cleveland, and the Laboratory of Histology and Embryology, Cornell University, Ithaca.) PLATES 66 TO 70, INTRODUCTION. Wilhelm Mfil.ler in I873 homologized the endostyle, or hypo- branchial groove, of the Tunicate, Amphioxus, and the larval Petro- myzon with the thyroid gland of all higher chordates. Subse- quent investigations have served to strengthen this remarkable homology, which would have been impossible of demonstration but for the survival of a single ctass of vertebrates, the Cyclostomes, of which the Petromyzontid~e, or Lampreys, are the best known order. The lamprey embraces in its own life history both the fullest devel- opment of the endostyle mechanisms and the characteristic ductless * Received for publication, December 3o, I912. 1I am indebted to Professor B. F. Kingsbury for the privileges of his labora- tory and for helpful criticisms and suggestions. I wish also to thank Professor S. H. Gage for helpful suggestions, and Mr. J. F. Badertscher for aid in many technical problems. 2In addition to the ventral midline subpharyngeal glandular structure, or endostyle proper, there are accessory structures directly continuous with the endostyle epithelium developed in the pharyngeal mucosa that are believed to function as the path of conduction for the slime cord issuing from the orifice of the endostyle. This function has not, however, been observed in the Am- mocoetes and is based on reasoning by analogy from Giard's (Giard, A., Arch. -
Vertebrates and Invertebrates
Vertebrates and invertebrates The animal kingdom is divided into two groups: vertebrates and invertebrates. Vertebrates have been around for millions of years but have evolved and changed over time. The word vertebrate means “having a backbone." Many animals have backbones. You have a backbone. So does a cow, a whale, a fish, a frog, and a bird. Vertebrates are animals that have a backbone. Most animals have a backbone that is made of bones joined together to form a skeleton. Our skeleton gives us our shape and allows us to move. Mammals, fish, birds, reptiles, and amphibians have Vertebrae backbones so they are all vertebrates. Each bone that makes up the backbone Scientists classify vertebrates into five classes: is called a vertebra. These are the • Mammals building blacks that form the backbone, • Fish also known as the spinal cord. The • Birds vertebrae protect and support your • Reptiles spine. Without a backbone, you would not • Amphibians be able to move any part of your body. Animals without a backbone are called invertebrates. Most The human animals are invertebrates. In fact, 95% of all living creatures backbone has 26 on Earth are invertebrates. vertebrae. Arthropods are the largest group of invertebrates. Insects make up a large part of this group. All insects, such as ladybugs, ants, grasshoppers, and bumblebees have three body sections and six legs. Most arthropods live on land, but some of these fascinating creatures live in water. Lobsters, crabs, and shrimp are arthropods that live in the oceans. Many invertebrates have skeletons on the outside of their A frog only has bodies called exoskeletons. -
Introduction to Phylum Chordata
Unifying Themes 1. Chordate evolution is a history of innovations that is built upon major invertebrate traits •bilateral symmetry •cephalization •segmentation •coelom or "gut" tube 2. Chordate evolution is marked by physical and behavioral specializations • For example the forelimb of mammals has a wide range of structural variation, specialized by natural selection 3. Evolutionary innovations and specializations led to adaptive radiations - the development of a variety of forms from a single ancestral group Characteristics of the Chordates 1. Notochord 2. dorsal hollow nerve cord 3. pharyngeal gill slits 4. postanal tail 5. endostyle Characteristics of the Chordates Notochord •stiff, flexible rod, provides internal support • Remains throughout the life of most invertebrate chordates • only in the embryos of vertebrate chordates Characteristics of the Chordates cont. Dorsal Hollow Nerve Cord (Spinal Cord) •fluid-filled tube of nerve tissue, runs the length of the animal, just dorsal to the notochord • Present in chordates throughout embryonic and adult life Characteristics of the Chordates cont. Pharyngeal gill slits • Pairs of opening through the pharynx • Invertebrate chordates use them to filter food •In fishes the gill sits develop into true gills • In reptiles, birds, and mammals the gill slits are vestiges (occurring only in the embryo) Characteristics of the Chordates cont. Endostyle • mucous secreting structure found in the pharynx floor (traps small food particles) Characteristics of the Chordates cont. Postanal Tail • works with muscles (myomeres) & notochord to provide motility & stability • Aids in propulsion in nonvertebrates & fish but vestigial in later lineages SubPhylum Urochordata Ex: tunicates or sea squirts • Sessile as adults, but motile during the larval stages • Possess all 5 chordate characteristics as larvae • Settle head first on hard substrates and undergo a dramatic metamorphosis • tail, notochord, muscle segments, and nerve cord disappear SubPhylum Urochordata cont. -
Kclo4 Inhibits Thyroidal Activity in the Larval Lamprey Endostyle in Vitro
GENERAL AND COMPARATIVE ENDOCRINOLOGY General and Comparative Endocrinology 128 (2002) 214–223 www.academicpress.com KClO4 inhibits thyroidal activity in the larval lamprey endostyle in vitro Richard G. Manzon*,1 and John H. Youson Department of Zoology and Division of Life Sciences, University of Toronto at Scarborough, 1265 Military Trail, Toronto, Ont., Canada MIC 1A4 Accepted 5 July 2002 Abstract An in vitro experimental system was devised to assess the direct effects of the goitrogen, potassium perchlorate (KClO4), on ra- dioiodide uptake and organification by the larval lamprey endostyle. Organification refers to the incorporation of iodide into lamprey thyroglobulin (Tg). Histological and biochemical evidence indicated that endostyles were viable at the termination of a 4 h in vitro incubation. A single iodoprotein, designated as lamprey Tg, was identified in the endostylar homogenates by polyacrylamide gel electrophoresis and Western blotting. Lamprey Tg was immunoreactive with rabbit anti-human Tg serum and had an electrophoretic mobility similar to that of reduced porcine Tg. When KClO4 was added to the incubation medium, both iodide uptake and orga- nification by the endostyle were significantly reduced relative to controls as determined by gamma counting, and gel-autoradiography and densitometry, respectively. Western blotting showed that KClO4 significantly lowered the total amount of lamprey Tg in the endostyle. Based on the results of this in vitro investigation, we conclude that KClO4 acts directly on the larval lamprey endostyle to inhibit thyroidal activity. These data support a previous supposition from in vivo experimentation that KClO4 acts directly on the endostyle to suppress the synthesis of thyroxine and triiodothyronine, resulting in a decrease in the serum levels of these two hormones. -
Fins, Limbs, and Tails: Outgrowths and Axial Patterning in Vertebrate Evolution Michael I
Review articles Fins, limbs, and tails: outgrowths and axial patterning in vertebrate evolution Michael I. Coates1* and Martin J. Cohn2 Summary Current phylogenies show that paired fins and limbs are unique to jawed verte- brates and their immediate ancestry. Such fins evolved first as a single pair extending from an anterior location, and later stabilized as two pairs at pectoral and pelvic levels. Fin number, identity, and position are therefore key issues in vertebrate developmental evolution. Localization of the AP levels at which develop- mental signals initiate outgrowth from the body wall may be determined by Hox gene expression patterns along the lateral plate mesoderm. This regionalization appears to be regulated independently of that in the paraxial mesoderm and axial skeleton. When combined with current hypotheses of Hox gene phylogenetic and functional diversity, these data suggest a new model of fin/limb developmental evolution. This coordinates body wall regions of outgrowth with primitive bound- aries established in the gut, as well as the fundamental nonequivalence of pectoral and pelvic structures. BioEssays 20:371–381, 1998. 1998 John Wiley & Sons, Inc. Introduction over and again to exemplify fundamental concepts in biological Vertebrate appendages include an amazing diversity of form, theory. The striking uniformity of teleost pectoral fin skeletons from the huge wing-like fins of manta rays or the stumpy limbs of illustrated Geoffroy Saint-Hilair’s discussion of ‘‘special analo- frogfishes, to ichthyosaur paddles, the extraordinary fingers of gies,’’1 while tetrapod limbs exemplified Owen’s2 related concept aye-ayes, and the fin-like wings of penguins. The functional of ‘‘homology’’; Darwin3 then employed precisely the same ex- diversity of these appendages is similarly vast and, in addition to ample as evidence of evolutionary descent from common ances- various modes of locomotion, fins and limbs are also used for try. -
The First Tunicate from the Early Cambrian of South China
The first tunicate from the Early Cambrian of South China Jun-Yuan Chen*, Di-Ying Huang, Qing-Qing Peng, Hui-Mei Chi, Xiu-Qiang Wang, and Man Feng Nanjing Institute of Geology and Palaeontology, Nanjing 210008, China Edited by Michael S. Levine, University of California, Berkeley, CA, and approved May 19, 2003 (received for review February 27, 2003) Here we report the discovery of eight specimens of an Early bilaterally symmetrical and club-shaped, and it is divided into Cambrian fossil tunicate Shankouclava near Kunming (South a barrel-shaped anterior part and an elongated, triangular, China). The tunicate identity of this organism is supported by the posterior part, which is called the ‘‘abdomen’’ (8–10). The presence of a large and perforated branchial basket, a sac-like anterior part, which occupies more than half the length of the peri-pharyngeal atrium, an oral siphon with apparent oral tenta- body, is dominated by a large pharyngeal basket, whose walls cles at the basal end of the siphonal chamber, perhaps a dorsal are formed by numerous transversely oriented rods interpreted atrial pore, and an elongated endostyle on the mid-ventral floor of as branchial bars. These bars are not quite straight, as the the pharynx. As in most modern tunicates, the gut is simple and anterior ones are weakly ϾϾϾ-shaped and the posterior ones U-shaped, and is connected with posterior end of the pharynx at slightly ϽϽϽ-shaped (Figs. 1 A, B, F, and H, and 2). The total one end and with an atrial siphon at the other, anal end. -
Vertebrates in the Animal Kingdom
Science Enhanced Scope and Sequence – Grade 5 Vertebrates in the Animal Kingdom Strand Living Systems Topic Investigating characteristics of organisms Primary SOL 5.5 The student will investigate and understand that organisms are made of one or more cells and have distinguishing characteristics that play a vital role in the organism’s ability to survive and thrive in its environment. Key concepts include b) classification of organisms using physical characteristics, body structures, and behavior of the organism; c) traits of organisms that allow them to survive in their environment. Related SOL 5.1 The student will demonstrate an understanding of scientific reasoning, logic, and the nature of science by planning and conducting investigations in which a) items such as rocks, minerals, and organisms are identified using various classification keys. Background Information To study organisms, scientists first look at their characteristics and group the organisms based on the characteristics they share. Some animals are so small that they live on or inside other animals. Others, such as the giant squid, are many meters long and live in the depths of oceans. Animals can swim, crawl, burrow, fly, or not move at all. No matter what their size, where they live, or how they move, all animals must have some basic characteristics in common. All organisms in the animal kingdom (1)) are made of cells, (2 reproduce, (3) grow and develop, (4) have a life cycle, (5) obtain and use energy, and (6) responds and adapt to their environment. In the 18th century, a Swedish scientist named Carolus Linnaeus developed a system to organize living things. -
BLY 202 (Basic Chordates Zoology) Sub-Phylum Urochordata (Tunicata)
BLY 202 (Basic Chordates Zoology) Sub-Phylum Urochordata (Tunicata) Objectives are to; a) understand the characteristics of Urochordata b) have knowledge on Urochordata evolution c) understand the different classes and their physiology The urochordates (“tail-chordates”), more commonly called tunicates, include about 3000 species. Tunicates are also called sea squirts. They are found in all seas from near shoreline to great depths. Most are sessile as adults, although some are free living. The name “tunicate” is suggested by the usually tough, non-living tunic, or test that surrounds the animal and contains cellulose. As adults, tunicates are highly specialized chordates, for in most species only the larval form, which resembles a microscopic tadpole, bears all the chordate hallmarks. During adult metamorphosis, the notochord (which, in the larva, is restricted to the tail, hence the group name Urochordata) and the tail disappear altogether, while the dorsal nerve cord becomes reduced to a single ganglion. The body of the adult urochordates is unsegmented and lacks a tail. Nephrocytes are responsible for the excretion of urochordates. The asexual reproduction of urochordates occurs by budding. Urochordates are bisexual and the external fertilization is the mode of sexual reproduction. Urochordates have an unsegmented body. Urochordates are exclusively marine animal. The earliest probable species of tunicate appears in the fossil record in the early Cambrian period. Despite their simple appearance and very different adult form, their close relationship to the vertebrates is evidenced by the fact that during their mobile larval stage, they possess a notochord or stiffening rod and resemble a tadpole. Their name derives from their unique outer covering or "tunic", which is formed from proteins and carbohydrates, and acts as an exoskeleton. -
Evolutionary Crossroads in Developmental Biology: Cyclostomes (Lamprey and Hagfish) Sebastian M
PRIMER SERIES PRIMER 2091 Development 139, 2091-2099 (2012) doi:10.1242/dev.074716 © 2012. Published by The Company of Biologists Ltd Evolutionary crossroads in developmental biology: cyclostomes (lamprey and hagfish) Sebastian M. Shimeld1,* and Phillip C. J. Donoghue2 Summary and is appealing because it implies a gradual assembly of vertebrate Lampreys and hagfish, which together are known as the characters, and supports the hagfish and lampreys as experimental cyclostomes or ‘agnathans’, are the only surviving lineages of models for distinct craniate and vertebrate evolutionary grades (i.e. jawless fish. They diverged early in vertebrate evolution, perceived ‘stages’ in evolution). However, only comparative before the origin of the hinged jaws that are characteristic of morphology provides support for this phylogenetic hypothesis. The gnathostome (jawed) vertebrates and before the evolution of competing hypothesis, which unites lampreys and hagfish as sister paired appendages. However, they do share numerous taxa in the clade Cyclostomata, thus equally related to characteristics with jawed vertebrates. Studies of cyclostome gnathostomes, has enjoyed unequivocal support from phylogenetic development can thus help us to understand when, and how, analyses of protein-coding sequence data (e.g. Delarbre et al., 2002; key aspects of the vertebrate body evolved. Here, we Furlong and Holland, 2002; Kuraku et al., 1999). Support for summarise the development of cyclostomes, highlighting the cyclostome theory is now overwhelming, with the recognition of key species studied and experimental methods available. We novel families of non-coding microRNAs that are shared then discuss how studies of cyclostomes have provided exclusively by hagfish and lampreys (Heimberg et al., 2010). -
Sea Squirt) Capable of Metabolizing Iodine?
TITLE: Microbial Symbionts from the Endostyle Region of the Ascidiella aspersa (Sea Squirt) capable of metabolizing iodine? Indu Sharma, Phd Microbial Diversity Course 2017 Hampton University Abstract: Tunicates (sea squirt) are filter feeders which process liters of sea water daily. They have a preemptive organelle similar to the vertebrate thyroid called an endostyle. The endostyle has been identified as site for iodine metabolism. Our hypothesis was that microbial symbionts associated with endostyle play a role in iodine metabolism. Using Ascidiella aspersa (sea squirt) as the model, we have identified Endozoicomonas ascidiicola as a dominant symbiont of the endostyle and its surrounding tissues. We have found that the mucus secreted by the endostyle in the bronchial sac has an acidic pH providing a unique microbial environment. Indirect evidence from fluorescent microscopy suggest the Endozoicomons are present in tissue and not in the mucus layer and warrant further investigation. INTRODUCTION: The mechanism of uptake of iodine have been characterized in the thyroid gland of vertebrates, brown algae, and kelp. However, the microbial contribution of this uptake has never been studied in tunicates. This led to our hypothesis “Does the sea squirt, a tunicate, harbor microbial symbionts capable of metabolizing iodine/iodate from the sea water?” The sea squirt can filter hundreds of liter of sea water per day where iodine is primarily present in the form of iodide (I-) or iodate (IO3-). The concentration of iodide is higher in warm surface water (0.10 pg per liter on the average) than that in cold deeper water of lower temperature than 20°C (0.03pg per liter) (Tsunogai and Henmi, 1971).