Management of Invasive Vertebrates in the United States: an Overview
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Lowland Book 170618.Indd
Grey partridges are an “indicator species” for broader farmland biodiversity, because where they thrive, a range of other species tend to do well. © Markus Jenny 3. Grey partridge In the past, the wild grey partridge thrived on farmland, and was traditionally the main focus of shooting in the lowlands. Management for driven partridge shooting led to rising numbers during the 19th century; it involved comprehensive predator control in a farmed environment that provided good partridge habitat, with weedy cereal crops, traditional crop rotations including grass crops, small fields separated by hedges, fallows and waste ground. By contrast, grey partridge numbers have been falling in the UK throughout the second half of the 20th century, with the decline becoming most marked since the mid-1960s. To focus conservation efforts, the grey partridge was put on the UK Red Data List in 1990, became a priority species under the 1995 UK Biodiversity Action Plan36, and remains a red-listed Bird of Conservation Concern. Progress has been made in areas that make a commitment to partridge conservation, but overall the decline in their numbers continues. GWCT research on grey partridge declines in the 1960s and 1970s helped to establish the new field of agro-ecology, which is studying 38 39 The Knowledge ecology within farming systems. Scientific study moved from recording declines, to investigating the changes in the arable environment that were affecting partridges45–47. This work found that the causes of the grey partridge decline were directly or indirectly related to much wider declines in many aspects of farmland biodiversity. For instance, the UK government monitors national bird abundance through the British Trust for Ornithology’s Breeding Bird Survey, which has shown a 92% decline in numbers of grey partridge from 1967 to 2015, in conjunction with declines in many other species of farmland bird48. -
A Review of the Cnemidophorus Lemniscatus Group in Central America (Squamata: Teiidae), with Comments on Other Species in the Group
TERMS OF USE This pdf is provided by Magnolia Press for private/research use. Commercial sale or deposition in a public library or website is prohibited. Zootaxa 3722 (3): 301–316 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3722.3.1 http://zoobank.org/urn:lsid:zoobank.org:pub:4E9BA052-EEA9-4262-8DDA-E1145B9FA996 A review of the Cnemidophorus lemniscatus group in Central America (Squamata: Teiidae), with comments on other species in the group JAMES R. MCCRANIE1,3 & S. BLAIR HEDGES2 110770 SW 164th Street, Miami, Florida 33157-2933, USA. E-mail: [email protected] 2Department of Biology, 208 Mueller Laboratory, Pennsylvania State University, University Park, Pennsylvania 16802-5301, USA. E-mail: [email protected] 3Corresponding author. E-mail: [email protected] Abstract We provide the results of a morphological and molecular study on the Honduran Bay Island and mainland populations of the Cnemidophorus lemniscatus complex for which we resurrect C. ruatanus comb. nov. as a full species. Morphological comparison of the Honduran populations to Cnemidophorus populations from Panama led to the conclusion that the Pan- amanian population represents an undescribed species named herein. In light of these new results, and considering past morphological studies of several South American populations of the C. lemniscatus group, we suggest that three other nominal forms of the group are best treated as valid species: C. espeuti (described as a full species, but subsequently treat- ed as a synonym of C. lemniscatus or a subspecies of C. -
Small Game Review “Issues and Concerns”
ONTARIO FEDERATION OF ANGLERS AND HUNTERS SMALL GAME REVIEW “ISSUES AND CONCERNS” PRELIMINARY INPUT FROM THE ONTARIO FEDERATION OF ANGLERS AND HUNTERS OCTOBER 2009 General and Preliminary O.F.A.H. Comments/Suggestions Purpose The purpose is to update and revise the small game hunting regulations and policies, under the Fish and Wildlife Conservation Act, with the view to: • reflect changes in populations and/or harvest pressure to ensure sustainability; • address significant knowledge gaps where there is a conservation concern; • optimize the ecological, social, economic and recreational benefits that accrue through sustainable hunting of small game birds and mammals; • refine management directions and establish broad targets/objectives; and • manage and prevent human-wildlife conflicts. Scope of Review The review should include the conservation and management of provincial game birds, small game mammals, and furbearers that are also hunted (e.g. red fox, raccoon). At this time, small game species with current management plans/policy (i.e. wild turkey, wolves) need not be a focus within this review. The harvest management of migratory birds is primarily a federal mandate, but the review should consider recommendations for the improved management of migratory birds where there is a clear provincial interest and mandate to do so (e.g. woodcock, sandhill cranes). The harvest of snapping turtles and bullfrogs is regulated under the Fish and Wildlife Conservation Act, but are not considered “small game” for the purpose of this review. Falconry should be recognized as a small and growing method of small game hunting within Ontario; however, it should be mentioned that its regulation is reviewed regularly through the Provincial Falconry Advisory Committee, so it will not be included within this general review. -
What Makes a Good Alien? Dealing with the Problems of Non-Native Wildfowl Tony (A
What makes a good alien? Dealing with the problems of non-native wildfowl Tony (A. D.) Fox Mandarin Ducks Aix galericulata Richard Allen ABSTRACT Humans have been introducing species outside their native ranges as a source of food for thousands of years, but introductions of wildfowl have increased dramatically since the 1700s.The most serious consequence of this has been the extinction of endemic forms as a result of hybridisation, although competition between alien and native forms may also contribute to species loss. Globally, non-native wildfowl have yet to cause major disruption to ecosystem functions; introduce new diseases and parasites; cause anything other than local conflicts to agricultural and economic interests; or create major health and safety issues in ways that differ from native forms. The fact that this has not happened is probably simply the result of good fortune, however, since many introduced plants and animals have had huge consequences for ecosystems and human populations.The potential cost of greater environmental and economic damage, species extinction, and threats to the genetic and species diversity of native faunas means that we must do all we can to stop the deliberate or accidental introduction of species outside their natural range. International legislation to ensure this is remarkably good, but domestic law is generally weak, as is the political will to enforce such regulations.The case of the Ruddy Duck Oxyura jamaicensis in Europe will show whether control of a problem taxon can be achieved and underlines the financial consequences of dealing with introduced aliens.This paper was originally presented as the 58th Bernard Tucker Memorial Lecture to the Oxford Ornithological Society and the Ashmolean Natural History Society, in November 2008. -
The Importance of Assessing Climate Change Vulnerability to Address Species Conservation Karen E
Issues and Perspectives The Importance of Assessing Climate Change Vulnerability to Address Species Conservation Karen E. Bagne,* Megan M. Friggens, Sharon J. Coe, Deborah M. Finch U.S. Department of Agriculture Forest Service, Rocky Mountain Research Station, Albuquerque, New Mexico 87102 Present address of K.E. Bagne: Department of Biology, Kenyon College, Gambier, Ohio 43022 Abstract Species conservation often prioritizes attention on a small subset of ‘‘special status’’ species at high risk of extinction, but actions based on current lists of special status species may not effectively moderate biodiversity loss if climate change alters threats. Assessments of climate change vulnerability may provide a method to enhance identification of species at risk of extinction. We compared climate change vulnerability and lists of special status species to examine the adequacy of current lists to represent species at risk of extinction in the coming decades. The comparison was made for terrestrial vertebrates in a regionally important management area of the southwestern United States. Many species not listed as special status were vulnerable to increased extinction risk with climate change. Overall, 74% of vulnerable species were not included in lists of special status and omissions were greatest for birds and reptiles. Most special status species were identified as additionally vulnerable to climate change impacts and there was little evidence to indicate the outlook for these species might improve with climate change, which suggests that existing conservation efforts will need to be intensified. Current special status lists encompassed climate change vulnerability best if climate change was expected to exacerbate current threats, such as the loss of wetlands, but often overlooked climate-driven threats, such as exceeding physiological thresholds. -
The Bisexual Brain: Sex Behavior Differences and Sex Differences in Parthenogenetic and Sexual Lizards
BRAIN RESEARCH ELSEVIER Brain Research 663 (1994) 163-167 Short communication The bisexual brain: sex behavior differences and sex differences in parthenogenetic and sexual lizards Matthew S. Rand *, David Crews Institute of Reproductive Biology, Department of Zoology, University of Texas at Austin, Austin, TX 78712, USA Accepted 2 August 1994 Abstract The parthenogenetic lizard Cnemidophorus uniparens alternates in the display of male-like and female-like sexual behavior, providing a unique opportunity for determining the neuronal circuits subserving gender-typical sexual behavior within a single sex. Here we report a 6-fold greater [14C]2-fluoro-2-deoxyglucose uptake in the medial preoptic area of C. uniparens displaying male-like behavior in comparison with C. uniparens displaying female-like receptivity. The ventromedial nucleus of the hypothalamus showed greater 2DG accumulation in receptive C. uniparens than in courting C. uniparens. When a related sexual species (C. inornatus) was compared to the unisexual species, the anterior hypothalamus in C. inornatus males exhibited significantly greater activity. Keywords: 2-Deoxyglucose; Anterior hypothalamus; Medial preoptic area; Reptile; Ventromedial hypothalamus Female-typical and male-typical sex behavior are C. inornatus [7,17]. The aims of this study were to known to be integrated by specific hypothalamic nuclei determine: (1) if specific regions in the brains of in the vertebrate brain [6,18,22]. The ventromedial parthenogenetic and gonochoristic whiptail lizards ex- nucleus of the hypothalamus (VMH) and the medial hibit sexually dimorphic metabolic activity, as mea- preoptic area (mPOA) are involved in sexual receptiv- sured by the accumulation of [14C]2-fluoro-2-de- ity in females and both the mPOA and anterior hy- oxyglucose (2DG) in the brain during mating behavior, pothalamus (AH) play an important role in the regula- and (2) if these dimorphisms complement previous tion of copulatory behavior in males [6,18,19,22]. -
(Tantilla Oolitica) in Miami-Dade and Monroe Counties, Florida
Assessment of the Status and Distribution of the Endemic Rim Rock Crowned Snake (Tantilla oolitica) in Miami-Dade and Monroe Counties, Florida Final Report Grant Agreement #401817G006 Kirsten N. Hines and Keith A. Bradley July 10, 2009 Submitted by: The Institute for Regional Conservation 22601 S.W. 152 Avenue, Miami, FL 33170 George D. Gann, Executive Director Submitted to: Paula Halupa Fish and Wildlife Biologist U.S. Fish and Wildlife Service 1339 20th Street Vero Beach, FL 32960 1 Project Background: The rim rock crowned snake (Tantilla oolitica) is one of three species of small, burrowing snakes within the genus Tantilla found in Florida. Of the more than 40 species of this genus extending from the southeastern United States down to northern Argentina in South America, T. oolitica has the most limited distribution (Wilson 1982, Scott 2004). Confined to the Miami Rock Ridge in southeastern Miami-Dade County and parts of the Florida Keys in Monroe County, this species has been greatly affected by the rapid urbanization of this area. By 1975 it had already made the Florida State list of threatened species and it is currently considered a candidate for the Federal Endangered Species List. Traditionally, T. oolitica habitat included rockland hammocks and pine rocklands. Less than 2% of the pine rocklands on the Miami Rock Ridge currently remain (Snyder et. al 1990, USFWS 1999) and rockland hammocks both in Miami-Dade County and throughout the Florida Keys have been reduced to less than half their original extent and continue to face threat of development (Enge et. al 1997, USFWS 1999). -
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. -
White Sands Department of the Interior White Sands National Monument
National Park Service White Sands Department of the Interior White Sands National Monument Common Animal Species List NPS Photo/© Sally King Sally Photo/© NPS hite Sands National Monument is home to over 500 different animal Wspecies. Despite the harsh environment of the dunefield, these incredible creatures have learned to adapt and survive in this southern New Mexico desert. While many of these animals are nocturnal, there are still signs of their activity well into the daylight hours. Keep your eyes open and watch for evidence of the many animal species, both large and small, that call White Sands their home. Amphibians Commonly Seen: 6 Species Great Plains Toad Spadefoot Toads (three species) Reptiles Commonly Seen: 26 Species Lizards Snakes Bleached Earless Lizard Plains Blackhead Snake Collared Lizard Prarie Rattlesnake Desert Spiny Lizard Sonora Gopher Snake Horned Lizard (two species) Western Coachwhip Snake Little Striped Whiptail Lizard Western Diamondback Snake Long-nosed Leopard Lizard New Mexico Whiptail Lizard Southern Prarie Lizard Mammals Commonly Seen: 44 Species Apache Pocket Mouse Grey Fox Badger Kit Fox Blacktail Jackrabbit Kangaroo Rat Bobcat Oryx (African) Coyote Pallid Bat Deer Mouse Porcupine Desert Cottontail White-footed Mouse Desert Pocket Gopher Woodrat (three species) Fish White Sands Pupfish 1 Species Invertebrates Commonly Seen: 500+ Species Black Widow Nevada Buck Moth Caterpillar 100+ Families Camel Cricket Tarantula 12 Orders Carpenter Bee Tarantula Hawk Wasp Darkling Beetle White-Lined Sphinx Moth To learn more about White Sands, visit http://www.nps.gov/whsa The Mexican spadefoot toad is the breed and feed on insects. These official state amphibian of New amphibians lay eggs in the pools of Mexico and gets its name from the water that form during this rainy distinctive spade-like projections season. -
Endoparasites Infecting Two Species of Whiptail Lizard (<I
SHORT NOTES SHORT NOTES 1980; Ribas et al., 1995; 1998; Vrcibradic et al., 2000; Menezes et al., 2004). In this study we survey the en- doparasite faunas of two sympatric species of whiptail HERPETOLOGICAL JOURNAL, Vol. 15, pp. 133-137 (2005) lizards from Brazil, Cnemidophorus abaetensis Dias, ENDOPARASITES INFECTING TWO Rocha & Vrcibradic, 2002 and Cnemidophorus ocellifer (Spix, 1824). Cnemidophorus abaetensis is a recently SPECIES OF WHIPTAIL LIZARD described species whose geographic distribution is ap- (CNEMIDOPHORUS ABAETENSIS AND parently restricted to the northern coast of Bahia state C. OCELLIFER; TEIIDAE) IN A (Dias et al., 2002), whereas C. ocellifer is widespread in ‘RESTINGA’ HABITAT OF NORTH- South America south of the Amazonian region, from EASTERN BRAZIL north-eastern and central Brazil to Paraguay, Bolivia and northern Argentina (Vanzolini et al., 1980; Cei, EDUARDO JOSÉ R. DIAS, DAVOR VRCIBRADIC 1993). So far, nothing has been published about the AND CARLOS FREDERICO D. ROCHA endoparasites associated with these two species [in the study of Ribas et al., (1995) regarding nematodes of C. Setor de Ecologia, Instituto de Biologia, Universidade do ocellifer, the species under treatment is actually C. Estado do Rio de Janeiro, Rua São Francisco Xavier littoralis Rocha, Araújo, Vrcibradic & Costa, 2000, 524, 20550-011, Rio de Janeiro, RJ, Brazil which had not yet been formally described at the time We analysed the endoparasite fauna associated with (see Rocha et al., 2000a)]. two species of whiptail lizard (Cnemidophorus A total of 73 lizards (33 C. abaetensis and 40 C. abaetensis and C. ocellifer) from north-eastern Brazil. ocellifer) were collected by the first author with the aid Overall parasite prevalence was relatively low for both of elastic rubber bands at the coastal sand-dune species (18.2% in C. -
Testis Development and Differentiation in Amphibians
G C A T T A C G G C A T genes Review Testis Development and Differentiation in Amphibians Álvaro S. Roco , Adrián Ruiz-García and Mónica Bullejos * Departamento de Biología Experimental, Facultad de Ciencias Experimentales, Campus Las Lagunillas S/N, Universidad de Jaén, 23071 Jaén, Spain; [email protected] (Á.S.R.); [email protected] (A.R.-G.) * Correspondence: [email protected]; Tel.: +34-953-212770 Abstract: Sex is determined genetically in amphibians; however, little is known about the sex chromosomes, testis-determining genes, and the genes involved in testis differentiation in this class. Certain inherent characteristics of the species of this group, like the homomorphic sex chromosomes, the high diversity of the sex-determining mechanisms, or the existence of polyploids, may hinder the design of experiments when studying how the gonads can differentiate. Even so, other features, like their external development or the possibility of inducing sex reversal by external treatments, can be helpful. This review summarizes the current knowledge on amphibian sex determination, gonadal development, and testis differentiation. The analysis of this information, compared with the information available for other vertebrate groups, allows us to identify the evolutionarily conserved and divergent pathways involved in testis differentiation. Overall, the data confirm the previous observations in other vertebrates—the morphology of the adult testis is similar across different groups; however, the male-determining signal and the genetic networks involved in testis differentiation are not evolutionarily conserved. Keywords: amphibian; sex determination; gonadal differentiation; testis; sex reversal Citation: Roco, Á.S.; Ruiz-García, A.; Bullejos, M. Testis Development and Differentiation in Amphibians. -
Evolutionary History of Spiny- Tailed Lizards (Agamidae: Uromastyx) From
Received: 6 July 2017 | Accepted: 4 November 2017 DOI: 10.1111/zsc.12266 ORIGINAL ARTICLE Evolutionary history of spiny- tailed lizards (Agamidae: Uromastyx) from the Saharo- Arabian region Karin Tamar1 | Margarita Metallinou1† | Thomas Wilms2 | Andreas Schmitz3 | Pierre-André Crochet4 | Philippe Geniez5 | Salvador Carranza1 1Institute of Evolutionary Biology (CSIC- Universitat Pompeu Fabra), Barcelona, The subfamily Uromastycinae within the Agamidae is comprised of 18 species: three Spain within the genus Saara and 15 within Uromastyx. Uromastyx is distributed in the 2Allwetterzoo Münster, Münster, Germany desert areas of North Africa and across the Arabian Peninsula towards Iran. The 3Department of Herpetology & systematics of this genus has been previously revised, although incomplete taxo- Ichthyology, Natural History Museum of nomic sampling or weakly supported topologies resulted in inconclusive relation- Geneva (MHNG), Geneva, Switzerland ships. Biogeographic assessments of Uromastycinae mostly agree on the direction of 4CNRS-UMR 5175, Centre d’Écologie Fonctionnelle et Évolutive (CEFE), dispersal from Asia to Africa, although the timeframe of the cladogenesis events has Montpellier, France never been fully explored. In this study, we analysed 129 Uromastyx specimens from 5 EPHE, CNRS, UM, SupAgro, IRD, across the entire distribution range of the genus. We included all but one of the rec- INRA, UMR 5175 Centre d’Écologie Fonctionnelle et Évolutive (CEFE), PSL ognized taxa of the genus and sequenced them for three mitochondrial and three Research University, Montpellier, France nuclear markers. This enabled us to obtain a comprehensive multilocus time- calibrated phylogeny of the genus, using the concatenated data and species trees. We Correspondence Karin Tamar, Institute of Evolutionary also applied coalescent- based species delimitation methods, phylogenetic network Biology (CSIC-Universitat Pompeu Fabra), analyses and model- testing approaches to biogeographic inferences.