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Semen Collection and Evaluation in Micrurus Corallinus
Herpetological Conservation and Biology 15(3):620–625. Submitted: 22 May 2020; Accepted: 12 November 2020; Published: 16 December 2020. SEMEN COLLECTION AND EVALUATION IN MICRURUS CORALLINUS RAFAELA ZANI COETI1,2,4, KALENA BARROS DA SILVA3, GIUSEPPE PUORTO3, SILVIA REGINA TAVAGLIA-CARDOSO3, AND SELMA MARIA DE ALMEIDA-SANTOS1,2 1Laboratório de Ecologia e Evolução, Instituto Butantan, 1500 Avenida Vital Brasil, São Paulo 05503–900, Brazil 2Programa de Pós Graduação em Anatomia dos Animais Domésticos e Silvestres, Universidade de São Paulo, 87 Avenida Professor Doutor Orlando Marques de Paiva, São Paulo 05508–270, Brazil 3Museu Biológico, Instituto Butantan, 1500 Avenida Vital Brasil, São Paulo 05503–900, Brazil 4Corresponding author, e-mail: [email protected] Abstract.—The Painted Coral Snake Micrurus corallinus is one of the Brazilian species kept in captivity to obtain venom for antivenom production. Difficulties in establishing a sizeable breeding colony make it necessary to find alternatives that increase the reproductive efficiency of captive individuals. Here, we tested a semen collection protocol and characterize the seminal parameters of captive M. corallinus. We collected semen during the mating season of the species (spring-summer) and were successful at every first attempt. Spermatozoa of M. corallinus are elongated and filiform, and the midpiece is the longest part. Sperm motility and progressive motility reached values of 80% and 3.6%, respectively, during the reproductive period of this species. Our results will allow further studies to improve husbandry, reproductive rates, and conservation of captive M. corallinus. Key Words.—reproduction; reproductive biotechniques; reptiles; sperm parameters INTRODUCTION and capture rates of individual M. corallinus in the wild (Roze 1996) are worrisome and also make it difficult to Reproductive biotechniques have been useful in establish a breeding colony with a substantial number implementing conservation projects for endangered of animals. -
Other Contributions
Other Contributions NATURE NOTES Amphibia: Caudata Ambystoma ordinarium. Predation by a Black-necked Gartersnake (Thamnophis cyrtopsis). The Michoacán Stream Salamander (Ambystoma ordinarium) is a facultatively paedomorphic ambystomatid species. Paedomorphic adults and larvae are found in montane streams, while metamorphic adults are terrestrial, remaining near natal streams (Ruiz-Martínez et al., 2014). Streams inhabited by this species are immersed in pine, pine-oak, and fir for- ests in the central part of the Trans-Mexican Volcanic Belt (Luna-Vega et al., 2007). All known localities where A. ordinarium has been recorded are situated between the vicinity of Lake Patzcuaro in the north-central portion of the state of Michoacan and Tianguistenco in the western part of the state of México (Ruiz-Martínez et al., 2014). This species is considered Endangered by the IUCN (IUCN, 2015), is protected by the government of Mexico, under the category Pr (special protection) (AmphibiaWeb; accessed 1April 2016), and Wilson et al. (2013) scored it at the upper end of the medium vulnerability level. Data available on the life history and biology of A. ordinarium is restricted to the species description (Taylor, 1940), distribution (Shaffer, 1984; Anderson and Worthington, 1971), diet composition (Alvarado-Díaz et al., 2002), phylogeny (Weisrock et al., 2006) and the effect of habitat quality on diet diversity (Ruiz-Martínez et al., 2014). We did not find predation records on this species in the literature, and in this note we present information on a predation attack on an adult neotenic A. ordinarium by a Thamnophis cyrtopsis. On 13 July 2010 at 1300 h, while conducting an ecological study of A. -
Y Coralillos Falsos (Serpentes: Colubridae) De Veracruz, México
Acta Zoológica ActaMexicana Zool. (n.s.)Mex. 22(3):(n.s.) 22(3)11-22 (2006) CORALILLOS VERDADEROS (SERPENTES: ELAPIDAE) Y CORALILLOS FALSOS (SERPENTES: COLUBRIDAE) DE VERACRUZ, MÉXICO Miguel A. DE LA TORRE-LORANCA1,3,4, Gustavo AGUIRRE-LEÓN1 y Marco A. LÓPEZ-LUNA2,4 1Instituto de Ecología, A. C., Departamento de Biodiversidad y Ecología Animal, Km. 2.5 Carr. Antigua a Coatepec No. 351, Cong. El Haya, C. P. 91070 Xalapa, Veracruz, MÉXICO. [email protected] 2Universidad Juárez Autónoma de Tabasco, División Académica de Ciencias Biológicas, Km. 0.5 Carretera Villahermosa-Cárdenas entronque a Bosques de Saloya, Villahermosa, Tabasco MÉXICO. [email protected] 3Dirección actual: Instituto Tecnológico Superior de Zongolica. Km 4 Carretera a la Compañia s/n, Tepetitlanapa, CP 95005 Zongolica, Veracruz, MÉXICO [email protected] 4Centro de Investigaciones Herpetológicas de Veracruz A. C. RESUMEN En el Estado de Veracruz se distribuyen cinco especies de coralillos verdaderos del género Micrurus y 14 especies de coralillos falsos de diferentes géneros de colúbridos, lo que hace más probables los encuentros con coralillos falsos. Sin embargo, la identificación por patrones de color entre coralillos verdaderos y falsos no es confiable, a causa de la variación del color inter e intraespecífica y a las semejanzas de coloración entre varias especies de estas dos familias de serpientes. Palabras clave: Colubridae, Elapidae, Micrurus, mimetismo, patrón de coloración, Veracruz ABSTRACT Five species of coral snakes genus Micrurus, and 14 species of mimic false coral snakes of different colubrid genera ocurr in Veracruz, making encounters with false coral snakes more likely. However, positive identification by color pattern between coral snakes and their mimics is not reliable because of inter and intraspecific color variation and similarities in coloration between several species of these two snake families. -
Xenosaurus Tzacualtipantecus. the Zacualtipán Knob-Scaled Lizard Is Endemic to the Sierra Madre Oriental of Eastern Mexico
Xenosaurus tzacualtipantecus. The Zacualtipán knob-scaled lizard is endemic to the Sierra Madre Oriental of eastern Mexico. This medium-large lizard (female holotype measures 188 mm in total length) is known only from the vicinity of the type locality in eastern Hidalgo, at an elevation of 1,900 m in pine-oak forest, and a nearby locality at 2,000 m in northern Veracruz (Woolrich- Piña and Smith 2012). Xenosaurus tzacualtipantecus is thought to belong to the northern clade of the genus, which also contains X. newmanorum and X. platyceps (Bhullar 2011). As with its congeners, X. tzacualtipantecus is an inhabitant of crevices in limestone rocks. This species consumes beetles and lepidopteran larvae and gives birth to living young. The habitat of this lizard in the vicinity of the type locality is being deforested, and people in nearby towns have created an open garbage dump in this area. We determined its EVS as 17, in the middle of the high vulnerability category (see text for explanation), and its status by the IUCN and SEMAR- NAT presently are undetermined. This newly described endemic species is one of nine known species in the monogeneric family Xenosauridae, which is endemic to northern Mesoamerica (Mexico from Tamaulipas to Chiapas and into the montane portions of Alta Verapaz, Guatemala). All but one of these nine species is endemic to Mexico. Photo by Christian Berriozabal-Islas. amphibian-reptile-conservation.org 01 June 2013 | Volume 7 | Number 1 | e61 Copyright: © 2013 Wilson et al. This is an open-access article distributed under the terms of the Creative Com- mons Attribution–NonCommercial–NoDerivs 3.0 Unported License, which permits unrestricted use for non-com- Amphibian & Reptile Conservation 7(1): 1–47. -
Annual Egg Hunt Attracts Crowd
Vol. 29 • APRIL 2018 Vol. 1 • SEP 2006 Annual Egg Hunt attracts Crowd n March 30th, dozens of kids lined up to search for hidden eggs, play games, Oand meet the Easter bunny. Barbara Smith, the HOA Onsite Director, the Social Committee members led by Jennifer Gardner, as well as some of the voting representatives, hid more than 10,000 eggs! Four separate areas were set up based on age groups, and everyone left with eggs in their basket. The eggs were gone in less than 15 minutes! Those who were lucky found golden eggs which had a ticket for a basket provided by our sponsors. Several tubs were set up to collect any unwanted plastic eggs, and residents stayed to play games and collect prizes. The weather was beautiful, and both kids and parents had a great time! Join us in thanking our sponsors listed on page 15. Preparations for Pool Season Begin Summer will be here before you know it. lifeguards are only at the “bucket” pool at If you already have an amenity key, you Quarry Park. Teens will need a picture ID can verify it is working by testing it at the with proof of age to enter the pools alone. grotto pool during pool hours. If your fam- Residents will notice improvements at ily doesn’t have a key yet, you can drop by both pools this year—both amenity the HOA office at 901 Crystal Falls Pkwy centers have AED devices, both pool and complete the form to obtain access. decks will have improved surfaces and Our swimming pools are open every Lifeguards are only present at the the grotto pool will have new plaster. -
Bradley and Rosen 2018-05-13.Docx
DEFINING SUITABLE HABITAT AND CONSERVATION STATUS FOR THE TUCSON SHOVEL-NOSED SNAKE (CHIONACTIS ANNULATA KLAUBERI) IN THE SONORAN DESERT Curtis M. Bradley, Center for Biological Diversity, Tucson, AZ; and Philip C. Rosen, University of Arizona, Tucson, AZ. Abstract.— The Tucson shovel-nosed snake (Chionactis annulata klauberi) is a small specialized colubrid associated with sandy loams of the elevated portions of the Lower Colorado River Valley Sonoran Desert in central Arizona. This taxon is a recently redefined subspecies based on genetic data, and may be extirpated in the Tucson region, including the type locality. A recent (USFWS 2014) decision against protecting it was based in part on an expansive definition of its geographic range and a habitat model. Here, we redefine the subspecies distribution by uniting published results of mitochondrial and nuclear DNA. We then present a new ecologically-based model of its original and current habitat using the machine learning algorithm Random Forests. The new model accurately matches known and estimated presence-absence data for this taxon, and is consistent with morphometrics and, largely, with color pattern variation. It estimates 60% less available habitat than the USFWS model. We estimate that 39% of the 1,255,946 ha (3,103,505 acres) of original habitat has been converted to urban developments, roads, agriculture, or otherwise altered non-habitat. Of the remaining 770,971 ha (1,905,108 acres), 60% is susceptible to habitat conversion in the region, with only 10.9% of habitat having current legal protection. Ongoing and projected urbanization and energy development in its flatland desert habitat present a bleak future for this subspecies. -
Life History Account for Western Threadsnake
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group WESTERN THREADSNAKE Rena humilis Family: LEPTOTYPHLOPIDAE Order: SQUAMATA Class: REPTILIA R045 Written by: R. Marlow Reviewed by: T. Papenfuss Edited by: R. Duke, J. Harris DISTRIBUTION, ABUNDANCE, AND SEASONALITY The western threadsnake (once known as the western blind snake) is widely distributed in southern California from the coast to the eastern border at elevations up to 1515 m (5000 ft). It seldom occurs in strictly sandy areas, alluvial flats or dry lakes. Little is known about abundance. A wide variety of habitats at lower elevations is occupied where conditions are suitable for burrowing, or hiding under surface objects and in crevices (Klauber 1940, Brattstrom 1953, Brattstrom and Schwenkmeyer 1951, Stebbins 1954, 1972). SPECIFIC HABITAT REQUIREMENTS Feeding: This snake eats ants, termites, their eggs, larvae and other soft-bodied insects (Stebbins 1954). Cover: This snake burrows, spending most of its time underground. It has also been taken under objects such as logs, rocks and among the roots of shrubs. They have also been taken under granite flakes (Stebbins 1954). Reproduction: No data. Water: The species seems to prefer moister habitats but is found in very arid environments, so permanent water is probably not required (Stebbins 1954). Pattern: This species prefers moist areas. In canyons, stony and sandy deserts, rocky slopes and boulder piles, and scrub. SPECIES LIFE HISTORY Activity Patterns: This snake appears on the surface at night but may be active underground at other times. Greatest seasonal activity occurs from April to August (Stebbins 1954). -
0 Natural Selection
PDF hosted at the Radboud Repository of the Radboud University Nijmegen The following full text is a publisher's version. For additional information about this publication click this link. http://hdl.handle.net/2066/94566 Please be advised that this information was generated on 2021-09-30 and may be subject to change. 170 Natural Selection: Finding Specimens in a Natural History Collection Marieke van Erp1, Antal van den Bosch2, Steve Hunt2, Marian van der Meij3, René Dekker3 and Piroska Lendvai4 1VU University Amsterdam, Department of Computer Sciences 2Tilburg center for Cognition and Communication, Tilburg University 3Netherlands Centre for Biodiversity Naturalis 4Research Institute for Linguistics, Hungarian Academy of Sciences 1,2,3The Netherlands 4Hungary 1. Introduction The natural history domain is rich in information. For hundreds of years, biodiversity researchers have collected specimens and samples, and meticulously recorded the how, what, and where of these objects of research. To retrace this information, however, deep knowledge of the collection and patience is necessary. Whereas traditional access methods (e.g., analysing paper logs of specimen finds) can be used for smaller collections, the sheer size of most current natural history collections prohibits this. At the same time, information technology has advanced to the point where it is able to capture the intricacies of biodiversity collection information and provide the first steps towards full digital access. The need for collection information access is dire, as lack of access impairs our ability to answer questions about species biodiversity, diversity and change through time (Scoble, 2010). Examples from the young field of biodiversity informatics stress that in order to assess and tackle problems such as predicting a species’ reaction to changing environment or prioritisation of preservation policies, digitisation of and access to (large) collection databases is imperative (Guralnick & Hill, 2009; Johnson, 2007; Raes, 2009; Soberón & Peterson, 2004). -
Reptiles of Phil Hardberger Park
ALAMO AREA MASTER NATURALISTS & PHIL HARDBERGER PARK CONSERVANCY REPTILES OF PHIL HARDBERGER PARK ROSEBELLY LIZARD→ REPTILE= Rosebelly Lizard (picture by author) TERRESTRIAL Fred Wills is the author of this piece. VERTEBRATE Animals with backbones (vertebrates) fall into several classes. We all recognize feathered birds and hairy mammals. But what is a reptile? An easy defini- tion of reptiles is that they are terrestrial, vertebrate animals with scales or plates covering the body. However, this definition simplifies their great diversity. WITH SCALES In Texas alone, there are four major groups of reptiles: lizards, snakes, turtles, and crocodilians (alligators). Hardberger Park is home to lizards, snakes, and turtles. OR PLATES Common lizards of the park include the Rosebelly Lizard, Texas Spiny Lizard, and Ground Skink. Common snakes of the park include the Texas Rat Snake, Rough Earth Snake, and Checkered Garter Snake. Can you name any other lizards and snakes found in the area? Hint: One lizard can change color, and PHP: one snake can produce sound. ROSEBELLY LIZARD Like many birds and mammals, reptiles are predators. Small ones like the Rosebelly Lizard and Rough Earth Snake eat invertebrate animals such as insects. TEXAS SPINY LIZARD Medium-sized snakes such as the Checkered Garter Snake often eat frogs. Larger snakes, including the Texas Rat Snake, typically eat small mammals and GROUND SKINK birds. TEXAS RAT SNAKE Where do reptiles live? The various species occupy almost all kinds of habitats, from dry prairie to moist woodland, and even wetlands and streams. Re- ROUGH EARTH SNAKE lated species often divide up the habitat through differing behaviors. -
Fluorescence Emission in a Marine Snake
Galaxea, Journal of Coral Reef Studies 21: 7-8(2019) Photogallery Fluorescence emission in a marine snake Takashi SEIKO and Yohey TERAI SOKENDAI (The Graduate University for Advanced Studies), Department of Evolutionary Studies of Biosystems, Shonan Village, Hayama, Kanagawa 240-0193, Japan. Corresponding authors: Y. Terai, T. Seiko Emails: [email protected]; [email protected] Communicated by Frederic Sinniger (Associate EditorsinChief) Keywords fluorescence, Laticauda, marine reptile, sea krait Coral reefs are one of the most colorful environments on Earth. Light in coral reefs includes fluorescence as well as reflectance of sunlight. In fluorescence, mole cules are excited by illuminating light and emit longer wavelength fluorescence than the excitation light wave length. In coral reefs, fluorescent light emission is observed in a range of taxa including cnidarians (e.g. corals), arthropods and fishes (e.g., Johnsen 2012). In marine reptiles, fluorescent emission has reported thus far only from sea turtles (Gruber and Sparks 2015). Here we report fluorescent light emission in a marine snake. Laticauda laticaudata Linnaeus, 1758 is a semi aquatic sea krait (Elapidae: Laticaudinae) often ob served in coral reefs. We examined a specimen that was freshly frozen after death and subsequently thawed. This speci men was caught at Oganzaki, Ishigaki island, Oki nawa, Japan (24°27′12.4″N; 124°04′37.4″E) Fig. 1 Photographs of a sea krait (Laticauda laticaudata) illuminated with white light (A) without a filter, and ultraviolet LED light (B) through a blue light cutting filter (<490 nm). (C) A reflectance and fluorescence light spectrum measured from a pale band. -
Effects of Habitat on Clutch Size of Ornate Tree Lizards, Urosaurus Ornatus
Western North American Naturalist Volume 71 Number 2 Article 12 8-12-2011 Effects of habitat on clutch size of ornate tree lizards, Urosaurus ornatus Gregory Haenel Elon University, Elon, North Carolina, [email protected] Follow this and additional works at: https://scholarsarchive.byu.edu/wnan Part of the Anatomy Commons, Botany Commons, Physiology Commons, and the Zoology Commons Recommended Citation Haenel, Gregory (2011) "Effects of habitat on clutch size of ornate tree lizards, Urosaurus ornatus," Western North American Naturalist: Vol. 71 : No. 2 , Article 12. Available at: https://scholarsarchive.byu.edu/wnan/vol71/iss2/12 This Article is brought to you for free and open access by the Western North American Naturalist Publications at BYU ScholarsArchive. It has been accepted for inclusion in Western North American Naturalist by an authorized editor of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. Western North American Naturalist 71(2), © 2011, pp. 247–256 EFFECTS OF HABITAT ON CLUTCH SIZE OF ORNATE TREE LIZARDS, UROSAURUS ORNATUS Gregory Haenel1 ABSTRACT.—Clutch size is an important determinant of female reproductive success in reptiles. Although female body size explains much variation in clutch size, other important factors include differences in food availability, predation risk, morphology, and demography. Ornate tree lizards, Urosaurus ornatus, display extensive variation in life history traits, including clutch size. Tree lizards primarily use 2 distinct habitat types—trees and rock surfaces—which influence both the performance and morphology of this species and may affect life history traits such as clutch size. As food availability, micro- climate, and, potentially, predator escape probabilities differ between these 2 habitats, I predicted that tree- and rock- dwelling lizards would allocate resources toward clutch size differently. -
0 Natural Selection
PDF hosted at the Radboud Repository of the Radboud University Nijmegen The following full text is a publisher's version. For additional information about this publication click this link. http://hdl.handle.net/2066/94566 Please be advised that this information was generated on 2021-09-27 and may be subject to change. 170 Natural Selection: Finding Specimens in a Natural History Collection Marieke van Erp1, Antal van den Bosch2, Steve Hunt2, Marian van der Meij3, René Dekker3 and Piroska Lendvai4 1VU University Amsterdam, Department of Computer Sciences 2Tilburg center for Cognition and Communication, Tilburg University 3Netherlands Centre for Biodiversity Naturalis 4Research Institute for Linguistics, Hungarian Academy of Sciences 1,2,3The Netherlands 4Hungary 1. Introduction The natural history domain is rich in information. For hundreds of years, biodiversity researchers have collected specimens and samples, and meticulously recorded the how, what, and where of these objects of research. To retrace this information, however, deep knowledge of the collection and patience is necessary. Whereas traditional access methods (e.g., analysing paper logs of specimen finds) can be used for smaller collections, the sheer size of most current natural history collections prohibits this. At the same time, information technology has advanced to the point where it is able to capture the intricacies of biodiversity collection information and provide the first steps towards full digital access. The need for collection information access is dire, as lack of access impairs our ability to answer questions about species biodiversity, diversity and change through time (Scoble, 2010). Examples from the young field of biodiversity informatics stress that in order to assess and tackle problems such as predicting a species’ reaction to changing environment or prioritisation of preservation policies, digitisation of and access to (large) collection databases is imperative (Guralnick & Hill, 2009; Johnson, 2007; Raes, 2009; Soberón & Peterson, 2004).