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§4-71-6.5 LIST of CONDITIONALLY APPROVED ANIMALS November
§4-71-6.5 LIST OF CONDITIONALLY APPROVED ANIMALS November 28, 2006 SCIENTIFIC NAME COMMON NAME INVERTEBRATES PHYLUM Annelida CLASS Oligochaeta ORDER Plesiopora FAMILY Tubificidae Tubifex (all species in genus) worm, tubifex PHYLUM Arthropoda CLASS Crustacea ORDER Anostraca FAMILY Artemiidae Artemia (all species in genus) shrimp, brine ORDER Cladocera FAMILY Daphnidae Daphnia (all species in genus) flea, water ORDER Decapoda FAMILY Atelecyclidae Erimacrus isenbeckii crab, horsehair FAMILY Cancridae Cancer antennarius crab, California rock Cancer anthonyi crab, yellowstone Cancer borealis crab, Jonah Cancer magister crab, dungeness Cancer productus crab, rock (red) FAMILY Geryonidae Geryon affinis crab, golden FAMILY Lithodidae Paralithodes camtschatica crab, Alaskan king FAMILY Majidae Chionocetes bairdi crab, snow Chionocetes opilio crab, snow 1 CONDITIONAL ANIMAL LIST §4-71-6.5 SCIENTIFIC NAME COMMON NAME Chionocetes tanneri crab, snow FAMILY Nephropidae Homarus (all species in genus) lobster, true FAMILY Palaemonidae Macrobrachium lar shrimp, freshwater Macrobrachium rosenbergi prawn, giant long-legged FAMILY Palinuridae Jasus (all species in genus) crayfish, saltwater; lobster Panulirus argus lobster, Atlantic spiny Panulirus longipes femoristriga crayfish, saltwater Panulirus pencillatus lobster, spiny FAMILY Portunidae Callinectes sapidus crab, blue Scylla serrata crab, Samoan; serrate, swimming FAMILY Raninidae Ranina ranina crab, spanner; red frog, Hawaiian CLASS Insecta ORDER Coleoptera FAMILY Tenebrionidae Tenebrio molitor mealworm, -
Feeding, Anatomy and Digestive Enzymes of False Limpet Siphonaria Guamensis
World Journal of Fish and Marine Sciences 5 (1): 104-109, 2013 ISSN 2078-4589 © IDOSI Publications, 2013 DOI: 10.5829/idosi.wjfms.2013.05.01.66144 Feeding, Anatomy and Digestive Enzymes of False Limpet Siphonaria guamensis K.V.R. Murty, A. Shameem and K. Umadevi Department of Marine Living Resources Andhra University, Visakhapatnam 530 003, A.P., India Abstract: Very little information has been available in the literature on the feeding habits, anatomy and histology of digestive system of siphonariid limpets. The present study revealed Siphonaria guamensis feeds on the crustose red alga Hildenbrandia prototypus browsing on the rocks by rasping action of radula. The anatomy of digestive system of Siphonaria guamensis is similar with that of the other siphonariid limpets but the length of gut and colon are shorter than the patellogastropod limpets like Cellana radiata, patella vulgata, Fissurella barbadensis and species of Acmaea. The salivary glands are the main source of the enzyme system of Siphonaria guamensis. They contained enzymes which can act on carbohydrates, proteins and polysaccharides. The enzyme which can act on proteins was found only in salivary glands and not detected in any other part of the digestive system. No lypolytic activity was seen in any part of the digestive system of the animal. Key words: False Limpet Feeding Anatomy Digestive Enzymes INTRODUCTION tridentatum and C. minimum, where he described the morphology and histology of the digestive system at Little work has been done on the feeding, digestion length. anatomy and histology of the digestive organs of limpets Very little information has been available in the with an exception of patella vulgata (Davies and Fleure literature on the feeding methods, anatomy and histology [1], Graham [2], Stone and Morton [3], Fretter and Graham of the digestive system of siphonariid limpets. -
The Evolution of the Placenta Drives a Shift in Sexual Selection in Livebearing Fish
LETTER doi:10.1038/nature13451 The evolution of the placenta drives a shift in sexual selection in livebearing fish B. J. A. Pollux1,2, R. W. Meredith1,3, M. S. Springer1, T. Garland1 & D. N. Reznick1 The evolution of the placenta from a non-placental ancestor causes a species produce large, ‘costly’ (that is, fully provisioned) eggs5,6, gaining shift of maternal investment from pre- to post-fertilization, creating most reproductive benefits by carefully selecting suitable mates based a venue for parent–offspring conflicts during pregnancy1–4. Theory on phenotype or behaviour2. These females, however, run the risk of mat- predicts that the rise of these conflicts should drive a shift from a ing with genetically inferior (for example, closely related or dishonestly reliance on pre-copulatory female mate choice to polyandry in conjunc- signalling) males, because genetically incompatible males are generally tion with post-zygotic mechanisms of sexual selection2. This hypoth- not discernable at the phenotypic level10. Placental females may reduce esis has not yet been empirically tested. Here we apply comparative these risks by producing tiny, inexpensive eggs and creating large mixed- methods to test a key prediction of this hypothesis, which is that the paternity litters by mating with multiple males. They may then rely on evolution of placentation is associated with reduced pre-copulatory the expression of the paternal genomes to induce differential patterns of female mate choice. We exploit a unique quality of the livebearing fish post-zygotic maternal investment among the embryos and, in extreme family Poeciliidae: placentas have repeatedly evolved or been lost, cases, divert resources from genetically defective (incompatible) to viable creating diversity among closely related lineages in the presence or embryos1–4,6,11. -
Occasional Papers of the Museum of Zoology University of Michigan Ann Arbor, Michigan University of Michigan Press Vanishing
OCCASIONAL PAPERS OF THE MUSEUM OF ZOOLOGY UNIVERSITY OF MICHIGAN ANN ARBOR,MICHIGAN UNIVERSITYOF MICHIGANPRESS VANISHING AND EXTINCT COLONIES OF TREE SNAILS, LIGUUS PASCIATUX, IN THE VICINITY OF MIAMT, FLORIDA1 BY FRANKN. YOUNG Szib~nittedfor publicatio?~drine 15, 1950 TI-IE once numerous tropical hardwood hamrnocks in the region of Miami, Florida, are rapidly being enveloped or destroyed by the grow- ing mctropolitan and suburban area. With the destruction of these hammocks the colonies of tree snails, Liguus fasciatus, characteristic of this type of vegetational association are doomed to extinction. Many colonies are complctely lost; others are on the verge of extinc- tion and mnst surely disappear in a few more years. In view of this prospect, I believe that the followiilg notes on the location of the ham- mocBs and thcir associated colonies of Ligzcus will be of value to future workers studying the distribution, ecology, or genetics of this group of snails. Thc tree snails of the genus Liguus are colonial only because they are strictly limited to the subtropical jungle-hammocli associes and to subtropical hammock associes with the corresponding clirnax associa- tions of the Florida Keys and the souther11 mainland (see Davis, 1943). Clench and Fairchild (1939) have reviewed the taxonomy of the Florida forms, and the names used in the present paper are largely based 011 their worlr. I11 some instaiiccs I have retained names of variants placed by them ill synonymy. These names express nzore clearly the 1 Colltributioli No. 463 from the Dcpartme~itof Zoology, Indiana University. Prank N. Young Occ. Papers concept of color patterns which I wish to discuss. -
Tc & Forward & Owls-I-IX
USDA Forest Service 1997 General Technical Report NC-190 Biology and Conservation of Owls of the Northern Hemisphere Second International Symposium February 5-9, 1997 Winnipeg, Manitoba, Canada Editors: James R. Duncan, Zoologist, Manitoba Conservation Data Centre Wildlife Branch, Manitoba Department of Natural Resources Box 24, 200 Saulteaux Crescent Winnipeg, MB CANADA R3J 3W3 <[email protected]> David H. Johnson, Wildlife Ecologist Washington Department of Fish and Wildlife 600 Capitol Way North Olympia, WA, USA 98501-1091 <[email protected]> Thomas H. Nicholls, retired formerly Project Leader and Research Plant Pathologist and Wildlife Biologist USDA Forest Service, North Central Forest Experiment Station 1992 Folwell Avenue St. Paul, MN, USA 55108-6148 <[email protected]> I 2nd Owl Symposium SPONSORS: (Listing of all symposium and publication sponsors, e.g., those donating $$) 1987 International Owl Symposium Fund; Jack Israel Schrieber Memorial Trust c/o Zoological Society of Manitoba; Lady Grayl Fund; Manitoba Hydro; Manitoba Natural Resources; Manitoba Naturalists Society; Manitoba Critical Wildlife Habitat Program; Metro Propane Ltd.; Pine Falls Paper Company; Raptor Research Foundation; Raptor Education Group, Inc.; Raptor Research Center of Boise State University, Boise, Idaho; Repap Manitoba; Canadian Wildlife Service, Environment Canada; USDI Bureau of Land Management; USDI Fish and Wildlife Service; USDA Forest Service, including the North Central Forest Experiment Station; Washington Department of Fish and Wildlife; The Wildlife Society - Washington Chapter; Wildlife Habitat Canada; Robert Bateman; Lawrence Blus; Nancy Claflin; Richard Clark; James Duncan; Bob Gehlert; Marge Gibson; Mary Houston; Stuart Houston; Edgar Jones; Katherine McKeever; Robert Nero; Glenn Proudfoot; Catherine Rich; Spencer Sealy; Mark Sobchuk; Tom Sproat; Peter Stacey; and Catherine Thexton. -
Records Committee Report
138 Florida Field Naturalist 28(3):138-160, 2000. RECORDS COMMITTEE REPORT Thirteenth Report of the Florida Ornithological Society Records Commit- tee: 1996, 1997, 1998, 1999, and 2000.—The Florida Ornithological Society Records Committee (FOSRC) critically reviews all written sight reports and specimens and/or photographic records (including audio recordings) submitted to it to determine the validity of the reports. The Committee’s findings are published periodically in the Flor- ida Field Naturalist (FFN). Of the 65 reports received and logged in 1996 through June 2000, 6 were not reviewed for various reasons discussed subsequently, 1 was withdrawn, and 4 are still under consideration: Cassin’s Kingbird, Tyrannus vociferans (97-375); Thayer’s Gull, Larus thayeri (99-389); Tropical Kingbird, Tyrannus melancholicus (00- 402); and Black-headed Gull, Larus ridibundus (00-410). The committee considered 7 reports submitted prior to 1996. Of these, 1 was not reviewed. Thus of the 60 reports resolved, 36 (60%) were accepted and 24 (40%) were not accepted. Since 1996, 13 species were added to the official FOSRC list of accepted Florida spe- cies. In addition, Rufous-sided Towhee was split into Eastern Towhee and Spotted Towhee, both verified from Florida, and Sharp-tailed Sparrow was split into Nelson’s Sharp-tailed Sparrow and Saltmarsh Sharp-tailed Sparrow, also both verified from Flor- ida, bringing the total to 480 species (see R&W 1992, FFN 23:38-43, FFN 24:122-134) (Appendix 1). Since the publication of Robertson and Woolfenden (1992), hereafter -
Trip Details
Cuba’s Western Mountains, Zapata Peninsula, Northern Archipelago, Escambray Valley and Havana Spring Migration Cuba Bird Survey November 9 – 18/19, 2018 You are invited on an exclusive, U.S. led and managed birding program to Cuba! The program is managed by the Caribbean Conservation Trust, Inc. (CCT), which is based in Connecticut. In early 2018 CCT staff began their 22nd year of managing bird conservation and natural history programs in Cuba. Along with CCT Ornithologist Michael Good, our team will include award -winning Cuban artist, author, and naturalist Nils Navarro, a bilingual Cuban tour leader and local naturalists in 4 different birding regions. They will guide you through some of the best bird habitat in Cuba, the Caribbean’s largest and most ecologically diverse island nation. CCT designed this itinerary to take you to Cuba’s finest bird habitats, most beautiful national parks, diverse biosphere reserves, and unique natural areas. We will interact with local scientists and naturalists who work in research and conservation. In addition to birding, we will learn about the ecology and history of regions we visit. Finally, and especially given the ongoing changes in U.S. – Cuban relations, we can expect some degree of inquiry into fascinating aspects of Cuban culture, history, and daily living during our visit. Cuba’s Birds According to BirdLife International, which has designated 28 Important Bird Areas (IBAs) in Cuba, “Over 370 bird species have been recorded in Cuba, including 27 which are endemic to the island and 29 considered globally threatened. Due to it’s large land area and geographical position within the Caribbean, Cuba represents one of the most important countries for Neotropical migratory birds – both birds passing through on their way south (75 species) and those spending the winter on the island (86 species).“ Our itinerary provides opportunities to see many of Cuba’s endemic species and subspecies, as listed below. -
Profound Head Modifications in Claviger Testaceus (Pselaphinae, Staphylinidae, Coleoptera) Facilitate Integration Into Communities of Ants
Received: 15 April 2020 Revised: 8 June 2020 Accepted: 14 June 2020 DOI: 10.1002/jmor.21232 RESEARCH ARTICLE Profound head modifications in Claviger testaceus (Pselaphinae, Staphylinidae, Coleoptera) facilitate integration into communities of ants Paweł Jałoszynski 1 | Xiao-Zhu Luo2 | Rolf Georg Beutel2 1Museum of Natural History, University of Wrocław, Wrocław, Poland Abstract 2Institut für Zoologie und Evolutionsforschung, Clavigeritae is a group of obligate myrmecophiles of the rove beetle subfamily Friedrich Schiller Universität Jena, Jena, Pselaphinae (Staphylinidae). Some are blind and wingless, and all are believed to Germany depend on ant hosts through feeding by trophallaxis. Phylogenetic hypotheses sug- Correspondence gest that their ancestors, as are most pselaphines today, were free-living predators. Paweł Jałoszynski, Museum of Natural History, University of Wrocław, Sienkiewicza Morphological alterations required to transform such beetles into extreme myrmeco- ł 21, 50 335 Wroc aw, Poland. philes were poorly understood. By studying the cephalic morphology of Claviger tes- Email: [email protected] taceus, we demonstrate that profound changes in all mouthpart components took Funding information place during this process, with a highly unusual connection of the maxillae to the AEI/FEDER, UE, Grant/Award Number: CGL2013 48950 C2 hypopharynx, and formation of a uniquely transformed labium with a vestigial prementum. The primary sensory function of the modified maxillary and labial palps is reduced, and the ventral mouthparts transformed into a licking/‘sponging’ device. Many muscles have been reduced, in relation to the coleopteran groundplan or other staphylinoids. The head capsule contains voluminous glands whose appeasement secretions are crucial for the beetle survival in ant colonies. The brain, in turn, has been shifted into the neck region. -
Differential Algal Consumption by Three Species of <I>Fissurella</I
BULLETIN OF MARINE SCIENCE. 46(3): 735-748.1990 DIFFERENTIAL ALGAL CONSUMPTION BY THREE SPECIES OF FISSURELLA(MOLLUSCA:GASTROPODA)AT ISLA DE MARGARITA, VENEZUELA Craig J. Franz ABSTRACT Visual observations and gut analyses were used to determine types of food ingested by Fissurella nimbosa (Linnaeus, 1758), F. nodosa (Born, 1778), and F. barbadensis (Gmelin, 1791) at Isla de Margarita, Venezuela. Although these animals have a wide variety of algal sources from which to select and on which they appear to feed in an opportunistic fashion, specific food preferences exist. Fissurella nodosa prefers encrusting microalgae and diatoms; F. nimbosa ingests laminar sheets of predominantly brown algae; F. barbadensis feeds on a wide variety of algae but often selects coralline algae of which it ingests entire branches. In zones of overlap, it is hypothesized that competition for food among Fissurella species is minimal due to resource allocation through food preference. Laboratory experiments indicate that all three congeners can ingest a greater variety of algal types than they normally consume in the field. Differential food consumption indicates significantly more elaborate niche par- titioning among tropical intertidal Fissure/la than was previously known. Studies of comparative feeding among congeneric predators may provide insight into the manner by which organisms partition their environment. This partitioning may be achieved through spatial segregation, temporal allocation, or dietary pref- erence. In situations of spatial overlap and temporal feeding similarity, a unique opportunity exists to evaluate the way in which food preferences may help establish an individual's niche. In these circumstances, dietary studies of co-occurring congeners provides information concerning the partitioning of community food resources. -
Anatomical Evidence for Phylogenetic Relationships Among Woodpeckers
ANATOMICAL EVIDENCE FOR PHYLOGENETIC RELATIONSHIPS AMONG WOODPECKERS WILLIAM R. GOODGE ALT•tOUCr•the functionalanatomy of woodpeckershas long been a subjectof interest,their internal anatomyhas not been usedextensively for determiningprobable phylogeneticrelationships within the family. In part this is probablydue to the reluctanceto use highly adaptivefea- tures in phylogeneticstudies becauseof the likelihood of convergent evolution. Bock (1967) and othershave pointedout that adaptivehess in itself doesnot rule out taxonomicusefulness, and that the highly adaptivefeatures will probablybe the oneshaving conspicuous anatomical modifications,and Bock emphasizesthe need for detailedstudies of func- tion beforeusing featuresin studiesof phylogeny.Although valuable, functionalconclusions are often basedon inferencesnot backed up by experimentaldata. As any similaritybetween species is possiblydue to functionalconvergence, I believewhat is neededmost is detailedstudy of a numberof featuresin order to distinguishbetween similarities re- sultingfrom convergenceand thosebased on phylogenticrelationship. Simplestructures are not necessarilymore primitive and morphological trendsare reversible,as Mayr (1955) has pointedout. Individual varia- tion may occur and various investigatorsmay interpret structuresdif- ferently. Despite these limitations,speculation concerning phylogeny will continuein the future,and I believethat it shouldbe basedon more, rather than fewer anatomical studies. MATERIALS AND METItODS Alcoholic specimensrepresenting 33 genera -
Literature Cited in Lizards Natural History Database
Literature Cited in Lizards Natural History database Abdala, C. S., A. S. Quinteros, and R. E. Espinoza. 2008. Two new species of Liolaemus (Iguania: Liolaemidae) from the puna of northwestern Argentina. Herpetologica 64:458-471. Abdala, C. S., D. Baldo, R. A. Juárez, and R. E. Espinoza. 2016. The first parthenogenetic pleurodont Iguanian: a new all-female Liolaemus (Squamata: Liolaemidae) from western Argentina. Copeia 104:487-497. Abdala, C. S., J. C. Acosta, M. R. Cabrera, H. J. Villaviciencio, and J. Marinero. 2009. A new Andean Liolaemus of the L. montanus series (Squamata: Iguania: Liolaemidae) from western Argentina. South American Journal of Herpetology 4:91-102. Abdala, C. S., J. L. Acosta, J. C. Acosta, B. B. Alvarez, F. Arias, L. J. Avila, . S. M. Zalba. 2012. Categorización del estado de conservación de las lagartijas y anfisbenas de la República Argentina. Cuadernos de Herpetologia 26 (Suppl. 1):215-248. Abell, A. J. 1999. Male-female spacing patterns in the lizard, Sceloporus virgatus. Amphibia-Reptilia 20:185-194. Abts, M. L. 1987. Environment and variation in life history traits of the Chuckwalla, Sauromalus obesus. Ecological Monographs 57:215-232. Achaval, F., and A. Olmos. 2003. Anfibios y reptiles del Uruguay. Montevideo, Uruguay: Facultad de Ciencias. Achaval, F., and A. Olmos. 2007. Anfibio y reptiles del Uruguay, 3rd edn. Montevideo, Uruguay: Serie Fauna 1. Ackermann, T. 2006. Schreibers Glatkopfleguan Leiocephalus schreibersii. Munich, Germany: Natur und Tier. Ackley, J. W., P. J. Muelleman, R. E. Carter, R. W. Henderson, and R. Powell. 2009. A rapid assessment of herpetofaunal diversity in variously altered habitats on Dominica. -
Phenotypic Variation and the Behavioral Ecology of Lizards
Phenotypic Variation and the Behavioral Ecology of Lizards The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:40046431 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA Phenotypic Variation and the Behavioral Ecology of Lizards A dissertation presented by Ambika Kamath to The Department of Organismic and Evolutionary Biology in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the subject of Biology Harvard University Cambridge, Massachusetts March 2017 © 2017 Ambika Kamath All rights reserved. Dissertation Advisor: Professor Jonathan Losos Ambika Kamath Phenotypic Variation and the Behavioral Ecology of Lizards Abstract Behavioral ecology is the study of how animal behavior evolves in the context of ecology, thus melding, by definition, investigations of how social, ecological, and evolutionary forces shape phenotypic variation within and across species. Framed thus, it is apparent that behavioral ecology also aims to cut across temporal scales and levels of biological organization, seeking to explain the long-term evolutionary trajectory of populations and species by understanding short-term interactions at the within-population level. In this dissertation, I make the case that paying attention to individuals’ natural history— where and how individual organisms live and whom and what they interact with, in natural conditions—can open avenues into studying the behavioral ecology of previously understudied organisms, and more importantly, recast our understanding of taxa we think we know well.