Predation on a Cuban Brown Anole, Anolis Sagrei (Dactyloidae)
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
A Review of Sampling and Monitoring Methods for Beneficial Arthropods
insects Review A Review of Sampling and Monitoring Methods for Beneficial Arthropods in Agroecosystems Kenneth W. McCravy Department of Biological Sciences, Western Illinois University, 1 University Circle, Macomb, IL 61455, USA; [email protected]; Tel.: +1-309-298-2160 Received: 12 September 2018; Accepted: 19 November 2018; Published: 23 November 2018 Abstract: Beneficial arthropods provide many important ecosystem services. In agroecosystems, pollination and control of crop pests provide benefits worth billions of dollars annually. Effective sampling and monitoring of these beneficial arthropods is essential for ensuring their short- and long-term viability and effectiveness. There are numerous methods available for sampling beneficial arthropods in a variety of habitats, and these methods can vary in efficiency and effectiveness. In this paper I review active and passive sampling methods for non-Apis bees and arthropod natural enemies of agricultural pests, including methods for sampling flying insects, arthropods on vegetation and in soil and litter environments, and estimation of predation and parasitism rates. Sample sizes, lethal sampling, and the potential usefulness of bycatch are also discussed. Keywords: sampling methodology; bee monitoring; beneficial arthropods; natural enemy monitoring; vane traps; Malaise traps; bowl traps; pitfall traps; insect netting; epigeic arthropod sampling 1. Introduction To sustainably use the Earth’s resources for our benefit, it is essential that we understand the ecology of human-altered systems and the organisms that inhabit them. Agroecosystems include agricultural activities plus living and nonliving components that interact with these activities in a variety of ways. Beneficial arthropods, such as pollinators of crops and natural enemies of arthropod pests and weeds, play important roles in the economic and ecological success of agroecosystems. -
And Resurrection of Anolis (Diaphoranolis) Brooksi 1Steven Poe and 2Mason J
Ofcial journal website: Amphibian & Reptile Conservation amphibian-reptile-conservation.org 11(2) [General Section]: 1–16 (e141). urn:lsid:zoobank.org:pub:31FA8B4B-718B-4440-AE19-9E1AC95524BD Description of two new species similar to Anolis insignis (Squamata: Iguanidae) and resurrection of Anolis (Diaphoranolis) brooksi 1Steven Poe and 2Mason J. Ryan 1,3Department of Biology and Museum of Southwestern Biology, University of New Mexico, Albuquerque, New Mexico 87131, USA 2Arizona Game and Fish Department, 5000 W. Carefree Highway, Phoenix, AZ 85086, USA Abstract.—The spectacular giant anole lizard Anolis insignis is widely distributed but infrequently collected outside of northern Costa Rica. We recently collected several individuals similar to Anolis insignis from localities in Panama and southern Costa Rica. These populations difer from type locality A. insignis in male dewlap color and morphology. We associate one set of these populations with Anolis (Diaphoranolis) brooksi Barbour from Darién, Panama, and describe two additional populations as new species. Keywords. Central America, Costa Rica, lizard, Panama, Reptilia, taxonomy Citation: Poe S and Ryan MJ. 2017. Description of two new species similar to Anolis insignis (Squamata: Iguanidae) and resurrection of Anolis (Diaphoranolis) brooksi. Amphibian & Reptile Conservation 11(2) [General Section]: 1–16 (e141). Copyright: © 2017 Poe and Ryan. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial- NoDerivatives 4.0 International License, which permits unrestricted use for non-commercial and education purposes only, in any medium, provided the original author and the ofcial and authorized publication sources are recognized and properly credited. The ofcial and authorized publication credit sources, which will be duly enforced, are as follows: ofcial journal title Amphibian & Reptile Conservation; ofcial journal website <amphibian- reptile-conservation.org>. -
Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca
Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca John F. Lamoreux, Meghan W. McKnight, and Rodolfo Cabrera Hernandez Occasional Paper of the IUCN Species Survival Commission No. 53 Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca John F. Lamoreux, Meghan W. McKnight, and Rodolfo Cabrera Hernandez Occasional Paper of the IUCN Species Survival Commission No. 53 The designation of geographical entities in this book, and the presentation of the material, do not imply the expression of any opinion whatsoever on the part of IUCN concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. The views expressed in this publication do not necessarily reflect those of IUCN or other participating organizations. Published by: IUCN, Gland, Switzerland Copyright: © 2015 International Union for Conservation of Nature and Natural Resources Reproduction of this publication for educational or other non-commercial purposes is authorized without prior written permission from the copyright holder provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without prior written permission of the copyright holder. Citation: Lamoreux, J. F., McKnight, M. W., and R. Cabrera Hernandez (2015). Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca. Gland, Switzerland: IUCN. xxiv + 320pp. ISBN: 978-2-8317-1717-3 DOI: 10.2305/IUCN.CH.2015.SSC-OP.53.en Cover photographs: Totontepec landscape; new Plectrohyla species, Ixalotriton niger, Concepción Pápalo, Thorius minutissimus, Craugastor pozo (panels, left to right) Back cover photograph: Collecting in Chamula, Chiapas Photo credits: The cover photographs were taken by the authors under grant agreements with the two main project funders: NGS and CEPF. -
<I>ANOLIS</I> LIZARDS in the FOOD WEBS of STRUCTURALLY
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 12-2016 ASSESSING THE FUNCTIONAL SIMILARITY OF NATIVE AND INVASIVE ANOLIS LIZARDS IN THE FOOD WEBS OF STRUCTURALLY-SIMPLE HABITATS IN FLORIDA Nathan W. Turnbough University of Tennessee, Knoxville, [email protected] Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Part of the Terrestrial and Aquatic Ecology Commons Recommended Citation Turnbough, Nathan W., "ASSESSING THE FUNCTIONAL SIMILARITY OF NATIVE AND INVASIVE ANOLIS LIZARDS IN THE FOOD WEBS OF STRUCTURALLY-SIMPLE HABITATS IN FLORIDA. " PhD diss., University of Tennessee, 2016. https://trace.tennessee.edu/utk_graddiss/4174 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by Nathan W. Turnbough entitled "ASSESSING THE FUNCTIONAL SIMILARITY OF NATIVE AND INVASIVE ANOLIS LIZARDS IN THE FOOD WEBS OF STRUCTURALLY-SIMPLE HABITATS IN FLORIDA." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Doctor of Philosophy, with a major in Ecology and Evolutionary Biology. -
Sleep-Site Fidelity in Cuban Green
HTTPS://JOURNALS.KU.EDU/REPTILESANDAMPHIBIANSTABLE OF CONTENTS IRCF REPTILES & AMPHIBIANSREPTILES • VOL & AMPHIBIANS15, NO 4 • DEC 2008 • 28(2):189 245–247 • AUG 2021 IRCF REPTILES & AMPHIBIANS CONSERVATION AND NATURAL HISTORY TABLE OF CONTENTS Sleep-siteFEATURE ARTICLES Fidelity in Cuban Green Anoles, . Chasing Bullsnakes (Pituophis catenifer sayi) in Wisconsin: On the Road Anolisto Understanding the Ecology porcatus and Conservation of the Midwest’s Gray Giant Serpent ......................1840 Joshua M. Kapfer 190 . The Shared History of Treeboas (Corallus grenadensis) and Humans on Grenada: A Hypothetical Excursion(Squamata: ............................................................................................................................ Dactyloidae)Robert W. Henderson 198 RESEARCH ARTICLES . The Texas Horned Lizard in Central and Western TexasLuis ....................... F. de Armas Emily Henry, Jason Brewer, Krista Mougey, and Gad Perry 204 . The Knight Anole (Anolis equestris) in Florida .............................................P.O. Box 4327, SanBrian Antonio J. Camposano, de los Baños,Kenneth ArtemisaL. Krysko, Kevin38100, M. CubaEnge, Ellen([email protected]) M. Donlan, and Michael Granatosky 212 CONSERVATION ALERT Photographs by the author. World’s Mammals in Crisis ............................................................................................................................................................. 220 . More Than Mammals ..................................................................................................................................................................... -
Chromosome Evolution in Three Brazilian Leptodactylus Species
Hereditas 146: 104Á111 (2009) Chromosome evolution in three Brazilian Leptodactylus species (Anura, Leptodactylidae), with phylogenetic considerations JOA˜ O REINALDO CRUZ CAMPOS1, FERNANDO ANANIAS2, CINTHIA AGUIRRE BRASILEIRO3, MARCOS YAMAMOTO4,CE´ LIO FERNANDO BAPTISTA HADDAD1 and SANAE KASAHARA1 1Instituto de Biocieˆncias, Univ. Estadual Paulista, UNESP, Rio Claro, SP, Brasil 2Univ.Sa˜o Francisco, Braganc¸a Paulista, SP, Brasil 3Museu de Histo´ria Natural, UNICAMP, Campinas, SP, Brasil 4Depto do Meio Ambiente, Votorantim Celulose e Papel S/A, Santa Branca, SP, Brasil Campos, J. R. C., Ananias, F., Brasileiro, C. A., Yamamoto, M., Haddad, C. F. B. and Kasahara, S. 2009. Chromosome evolution in three Brazilian Leptodactylus species (Anura, Leptodactylidae), with phylogenetic considerations. * Hereditas 0146: 104Á111. Lund, Sweden. eISSN 1601-5223. Received September 29, 2008. Accepted December 22, 2008 Karyotypic analyses on three species of the Leptodactylus from Brazil showed 2n24 in L.cf.marmoratus,2n23 in Leptodactylus sp. (aff. bokermanni), and 2n26 in L. hylaedactylus, with distinct numbers of bi and uni-armed chromosomes. Leptodactylus cf. marmoratus presented a variation as regard to the morphology of pair 12. All specimens of L.cf.marmoratus had Ag-NOR in pair 6, confirmed by FISH, but the sample from one of the localities presented additional Ag-NOR, in one of the chromosomes 8. In Leptodactylus sp. (aff. bokermanni) and L. hylaedactylus the chromosome pairs bearing Ag-NOR are 11 and 7, respectively. The C banding patterns are predominantly centromeric, but only in L. marmoratus this heterochromatin appeared very brilliant with DAPI. On the other hand, bright labelling was noticed with CMA3 in the three species, on the Ag-NOR site. -
The Phylogenetic Distribution of Sphingomyelinase D Activity in Venoms of Haplogyne Spiders
Comparative Biochemistry and Physiology Part B 135 (2003) 25–33 The phylogenetic distribution of sphingomyelinase D activity in venoms of Haplogyne spiders Greta J. Binford*, Michael A. Wells Department of Biochemistry and Molecular Biophysics, University of Arizona, Tucson, AZ 85721, USA Received 6 October 2002; received in revised form 8 February 2003; accepted 10 February 2003 Abstract The venoms of Loxosceles spiders cause severe dermonecrotic lesions in human tissues. The venom component sphingomyelinase D (SMD) is a contributor to lesion formation and is unknown elsewhere in the animal kingdom. This study reports comparative analyses of SMD activity and venom composition of select Loxosceles species and representatives of closely related Haplogyne genera. The goal was to identify the phylogenetic group of spiders with SMD and infer the timing of evolutionary origin of this toxin. We also preliminarily characterized variation in molecular masses of venom components in the size range of SMD. SMD activity was detected in all (10) Loxosceles species sampled and two species representing their sister taxon, Sicarius, but not in any other venoms or tissues surveyed. Mass spectrometry analyses indicated that all Loxosceles and Sicarius species surveyed had multiple (at least four to six) molecules in the size range corresponding to known SMD proteins (31–35 kDa), whereas other Haplogynes analyzed had no molecules in this mass range in their venom. This suggests SMD originated in the ancestors of the Loxoscelesy Sicarius lineage. These groups of proteins varied in molecular mass across species with North American Loxosceles having 31–32 kDa, African Loxosceles having 32–33.5 kDa and Sicarius having 32–33 kDa molecules. -
For Submission As a Note Green Anole (Anolis Carolinensis) Eggs
For submission as a Note Green Anole (Anolis carolinensis) Eggs Associated with Nest Chambers of the Trap Jaw Ant, Odontomachus brunneus Christina L. Kwapich1 1Department of Biological Sciences, University of Massachusetts Lowell One University Ave., Lowell, Massachusetts, USA [email protected] Abstract Vertebrates occasionally deposit eggs in ant nests, but these associations are largely restricted to neotropical fungus farming ants in the tribe Attini. The subterranean chambers of ponerine ants have not previously been reported as nesting sites for squamates. The current study reports the occurrence of Green Anole (Anolis carolinensis) eggs and hatchlings in a nest of the trap jaw ant, Odontomachus brunneus. Hatching rates suggest that O. brunneus nests may be used communally by multiple females, which share spatial resources with another recently introduced Anolis species in their native range. This nesting strategy is placed in the context of known associations between frogs, snakes, legless worm lizards and ants. Introduction Subterranean ant nests are an attractive resource for vertebrates seeking well-defended cavities for their eggs. To access an ant nest, trespassers must work quickly or rely on adaptations that allow them to overcome the strict odor-recognition systems of ants. For example the myrmecophilous frog, Lithodytes lineatus, bears a chemical disguise that permits it to mate and deposit eggs deep inside the nests of the leafcutter ant, Atta cephalotes, without being bitten or harassed. Tadpoles inside nests enjoy the same physical and behavioral protection as the ants’ own brood, in a carefully controlled microclimate (de Lima Barros et al. 2016, Schlüter et al. 2009, Schlüter and Regös 1981, Schlüter and Regös 2005). -
Cfreptiles & Amphibians
HTTPS://JOURNALS.KU.EDU/REPTILESANDAMPHIBIANSTABLE OF CONTENTS IRCF REPTILES & AMPHIBIANSREPTILES • VOL15, & N AMPHIBIANSO 4 • DEC 2008 •189 28(1):30–31 • APR 2021 IRCF REPTILES & AMPHIBIANS CONSERVATION AND NATURAL HISTORY TABLE OF CONTENTS CoprophagyFEATURE ARTICLES and Cannibalism in the Cuban . Chasing Bullsnakes (Pituophis catenifer sayi) in Wisconsin: GreenOn the Road Anole,to Understanding the Ecology Anolis and Conservation of theporcatus Midwest’s Giant Serpent ...................... Gray Joshua M. Kapfer1840 190 . The Shared History of Treeboas (Corallus grenadensis) and Humans on Grenada: A Hypothetical Excursion(Squamata: ............................................................................................................................ Dactyloidae)Robert W. Henderson 198 RESEARCH ARTICLES . The Texas Horned Lizard in Central and Western TexasLuis ....................... F. de Armas Emily Henry, Jason Brewer, Krista Mougey, and Gad Perry 204 . The Knight Anole (Anolis equestris) in Florida .............................................P.O. Box 4327, San AntonioBrian J. deCamposano, los Baños, Kenneth Artemisa L. Krysko, Province Kevin 38100,M. Enge, Cuba Ellen M.([email protected]) Donlan, and Michael Granatosky 212 CONSERVATION ALERT . World’s Mammals in Crisis ............................................................................................................................................................. 220 oprophagy in. herbivorousMore Than Mammals reptiles, .............................................................................................................................. -
By the Wandering Spider Ctenus Ornatus (Araneae: Ctenidae) in Southeastern Brazil
Herpetology Notes, volume 8: 329-330 (2015) (published online on 16 June 2015) Predation on the tropical bullfrog Adenomera marmorata (Anura: Leptodactylidae) by the wandering spider Ctenus ornatus (Araneae: Ctenidae) in southeastern Brazil Lucas Coutinho Amaral¹,*, Pedro de Souza Castanheira², Sergio Potsch de Carvalho-e-Silva¹ and Renner Luiz Cerqueira Baptista² Anurans are common preys to some species of spiders tiny middle eyes and two large posterior eyes (Jocqué (Menin et al., 2005). Not only adults (e.g., Barej et al., and Dippenaar-Schoeman, 2006). Ctenids are nocturnal 2005), but also tadpoles are preyed on by spiders (e.g., hunters, running mainly on the leaf litter. They use mainly Folly et al., 2014a; Luiz et al., 2013). The frog species vibration and visual contact to locate prey, catching and Adenomera marmorata Steindachner, 1867, occurs in killing them with their powerful poison, delivered by the the Atlantic Rain Forest in southeastern Brazil, from fangs of their strong chelicerae (Jocqué and Dippenaar- Rio de Janeiro to Santa Catarina states (Frost, 2015), Schoeman, 2006). Ctenus ornatus (Keyserling, 1877) is and is one of the most abundant amphibian species in a large and very common ground spider in the Atlantic the leaf-litter (Heyer et al., 1990; Rocha et al., 2007). It Forest, distributed from Pernambuco state, in Northeast, is mostly a nocturnal frog, but males can also be heard to Goiás state, in the West, both in Brazil, to Misiones, at anytime of the day during rainy days (Izecksohn and Argentina (Brescovit and Simó, 2007). Carvalho-e-Silva, 2001). Males call from chambers The following event was observed during a dug in the ground, where the females lay their eggs herpetological field work at approximately 07:30 pm embedded in foam nests (Izecksohn and Carvalho-e- on 10 August, 2014, at the Centro Marista São José Silva, 2001). -
Ecological Functions of Neotropical Amphibians and Reptiles: a Review
Univ. Sci. 2015, Vol. 20 (2): 229-245 doi: 10.11144/Javeriana.SC20-2.efna Freely available on line REVIEW ARTICLE Ecological functions of neotropical amphibians and reptiles: a review Cortés-Gomez AM1, Ruiz-Agudelo CA2 , Valencia-Aguilar A3, Ladle RJ4 Abstract Amphibians and reptiles (herps) are the most abundant and diverse vertebrate taxa in tropical ecosystems. Nevertheless, little is known about their role in maintaining and regulating ecosystem functions and, by extension, their potential value for supporting ecosystem services. Here, we review research on the ecological functions of Neotropical herps, in different sources (the bibliographic databases, book chapters, etc.). A total of 167 Neotropical herpetology studies published over the last four decades (1970 to 2014) were reviewed, providing information on more than 100 species that contribute to at least five categories of ecological functions: i) nutrient cycling; ii) bioturbation; iii) pollination; iv) seed dispersal, and; v) energy flow through ecosystems. We emphasize the need to expand the knowledge about ecological functions in Neotropical ecosystems and the mechanisms behind these, through the study of functional traits and analysis of ecological processes. Many of these functions provide key ecosystem services, such as biological pest control, seed dispersal and water quality. By knowing and understanding the functions that perform the herps in ecosystems, management plans for cultural landscapes, restoration or recovery projects of landscapes that involve aquatic and terrestrial systems, development of comprehensive plans and detailed conservation of species and ecosystems may be structured in a more appropriate way. Besides information gaps identified in this review, this contribution explores these issues in terms of better understanding of key questions in the study of ecosystem services and biodiversity and, also, of how these services are generated. -
(Osteocephalus Taurinus) by Arthropods (Insecta, Mantodea and Arachnida, Araneae) in Central Brazil
Biota Neotrop., vol. 10, no. 3 Predation on young treefrog (Osteocephalus taurinus) by arthropods (Insecta, Mantodea and Arachnida, Araneae) in Central Brazil Raul Costa-Pereira1,5, Fernando Ibanez Martins2, Eurico Antonio Sczesny-Moraes3 & Antonio Brescovit4 1Centro de Ciências Biológicas e da Saúde – CCBS, Universidade Federal de Mato Grosso do Sul – UFMS, Cidade Universitária s/n, CEP 79070-900,Campo Grande, MS, Brasil 2Programa de Pós-graduação em Ecologia e Conservação, Centro de Ciências Biológicas e da Saúde – CCBS, Universidade Federal de Mato Grosso do Sul – UFMS, Cidade Universitária, s/n, CEP 79070-900, Campo Grande, MS, Brasil 3Departamento de Patologia, Centro de Ciências Biológicas e da Saúde – CCBS, Universidade Federal de Mato Grosso do Sul – UFMS, Cidade Universitária, s/n, CEP 79070-900, Campo Grande, MS, Brasil 4Laboratório de Artrópodes, Instituto Butantan, Av. Vital Brasil, 1500, CEP 05503-900, São Paulo, SP, Brasil 5Autor para correspondência: Raul Costa-Pereira, e-mail: [email protected] COSTA-PEREIRA, R., MARTINS, F.I., SCZESNY-MORAES, E.A. & BRASCOVIT, A. Predation on young treefrogs (Osteocephalus taurinus) by arthropods (Insecta, Mantodea and Arachnida, Araneae) in Central Brazil. Biota Neotrop. 10(3): http://www.biotaneotropica.org.br/v10n3/en/abstract?short- communication+bn04310032010. Abstract: Praying mantis and spider species are common food items in the diet of several anuran species. Nevertheless, in this study we report the predation of young treefrogs Osteocephalus taurinus by two spider species, a Pisauridae and a Trechaleidae (Neoctenus sp.) and by the praying mantis Eumusonia sp. in Mato Grosso, Central Brazil. The great abundance of this treefrog in the region, combined with its small body size during the juvenil stage, favor its predation by generalists predators.