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Tapera Dromococcyx
HOST LIST OF AVIAN BROOD PARASITES - 3 - CUCULIFORMES; Neomorphidae Peter E. Lowther, Field Museum version 14 Sep 2011 Tapera Tapera Thunberg 1819, Handlingar Kungl Vetenskaps och vitterheetssamhället i Göteborg, 3, p. 1. American Striped Cuckoo, Tapera naevia (Linnaeus) 1766 Systema Naturae, ed. 12, p. 170. Distribution. – Neotropics. General life history information found in Friedmann 1933, Belcher and Smooker 1936, Sick 1953, Haverschmidt 1955, 1961, Wetmore 1968, Morton and Farabaugh 1979, Salvador 1982, Payne 2005, Pulgarín-R. et al. 2007 (see also additional references in host list below). Host list. – From Friedmann 1933; see also Davis 1940, Loetscher 1952, Sick 1953, 1993, Haverschmidt 1955, 1961, 1968, Wetmore 1968 1, Salvador 1982, Kiff and Williams 1978, Payne 2005. Brief mention of this cuckoo in studies of actual or potential hosts given by: Skutch 1969, Thomas 1983, Freed 1987 2 TYRANNIDAE White-headed Marsh-Tyrant, Arundinicola leucocephala tody-flycatcher, Todirostrum spp. * (Sick 1953, 1993 lists species as “apparently also” a host) flycatcher, Myiozetetes spp. * (Sick 1953, 1993 lists species as “apparently also” a host) FURNARIIDAE Chotoy Spinetail, Schoeniophylax phryganophila Sooty-fronted Spinetail, Synallaxis frontalis Azara's Spinetail, Synallaxis azarae 3 (includes superciliosa) Pale-breasted Spinetail, Synallaxis albescens Spix’s Spinetail, Synallaxis spixi Plain-crowned Spinetail, Synallaxis gujanensis Rufous-breasted Spinetail, Synallaxis erythrothorax Stripe-breasted Spinetail, Synallaxis cinnamomea Yellow-chinned Spinetail, Certhiaxis cinnamomeus Short-billed Castanero, Asthenes [pyrrholeuca] baeri Plain Thornbird, Phacellodomus [rufifrons] rufifrons Greater Thornbird, Phacellodomus ruber Red-eyed Thornbird, Phacellodomus erythrophthalmus Buff-fronted Foliage-Gleaner, Philydor rufus TROGLODYTIDAE Rufous-and-white Wren, Thryothorus rufalbus Plain W ren, Thryothorus modestus EMBERIZIDAE Black-striped Sparrow, Arremonops conirostris Dromococcyx Dromococcyx W ied-Neuwied 1832, Beitrage zur Naturgeschichte von Brasil. -
Molecular Phylogeny of Cuckoos Supports a Polyphyletic Origin of Brood Parasitism
Molecular phylogeny of cuckoos supports a polyphyletic origin of brood parasitism S. ARAGO N,*A.P.MéLLER,*J.J.SOLER & M. SOLER *Laboratoire d'Ecologie, CNRS-URA 258, Universite Pierre et Marie Curie, BaÃt. A, 7e eÂtage, 7, quai St. Bernard, Case 237, F-75252 Paris Cedex 05, France Departamento de BiologõÂa Animal y EcologõÂa, Facultad de Ciencias, Universidad de Granada, E-18071 Granada, Spain Keywords: Abstract brood parasitism; We constructed a molecular phylogeny of 15 species of cuckoos using cuculiformes; mitochondrial DNA sequences spanning 553 nucleotide bases of the cyto- cytochrome b; chrome b gene and 298 nucleotide bases of the ND2 gene. A parallel analysis DNA sequencing; for the cytochrome b gene including published sequences in the Genbank ND2. database was performed. Phylogenetic analyses of the sequences were done using parsimony, a sequence distance method (Fitch-Margoliash), and a character-state method which uses probabilities (maximum likelihood). Phenograms support the monophyly of three major clades: Cuculinae, Phaenicophaeinae and Neomorphinae-Crotophaginae. Clamator, a strictly parasitic genus traditionally included within the Cuculinae, groups together with Coccyzus (a nonobligate parasite) and some nesting cuckoos. Tapera and Dromococcyx, the parasitic cuckoos from the New World, appear as sister genera, close to New World cuckoos: Neomorphinae and Crotophaginae. Based on the results, and being conscious that a more strict resolution of the relationships among the three major clades is required, we postulate that brood parasitism has a polyphyletic origin in the Cuculiformes, with parasite species being found within the three de®ned clades. Evidence suggests that species within each clade share a common parasitic ancestor, but some show partial or total loss of brood parasitic behaviour. -
Species Limits in Some Philippine Birds Including the Greater Flameback Chrysocolaptes Lucidus
FORKTAIL 27 (2011): 29–38 Species limits in some Philippine birds including the Greater Flameback Chrysocolaptes lucidus N. J. COLLAR Philippine bird taxonomy is relatively conservative and in need of re-examination. A number of well-marked subspecies were selected and subjected to a simple system of scoring (Tobias et al. 2010 Ibis 152: 724–746) that grades morphological and vocal differences between allopatric taxa (exceptional character 4, major 3, medium 2, minor 1; minimum score 7 for species status). This results in the recognition or confirmation of species status for (inverted commas where a new English name is proposed) ‘Philippine Collared Dove’ Streptopelia (bitorquatus) dusumieri, ‘Philippine Green Pigeon’ Treron (pompadora) axillaris and ‘Buru Green Pigeon’ T. (p.) aromatica, Luzon Racquet-tail Prioniturus montanus, Mindanao Racquet-tail P. waterstradti, Blue-winged Raquet-tail P. verticalis, Blue-headed Raquet-tail P. platenae, Yellow-breasted Racquet-tail P. flavicans, White-throated Kingfisher Halcyon (smyrnensis) gularis (with White-breasted Kingfisher applying to H. smyrnensis), ‘Northern Silvery Kingfisher’ Alcedo (argentata) flumenicola, ‘Rufous-crowned Bee-eater’ Merops (viridis) americanus, ‘Spot-throated Flameback’ Dinopium (javense) everetti, ‘Luzon Flameback’ Chrysocolaptes (lucidus) haematribon, ‘Buff-spotted Flameback’ C. (l.) lucidus, ‘Yellow-faced Flameback’ C. (l.) xanthocephalus, ‘Red-headed Flameback’ C. (l.) erythrocephalus, ‘Javan Flameback’ C. (l.) strictus, Greater Flameback C. (l.) guttacristatus, ‘Sri Lankan Flameback’ (Crimson-backed Flameback) Chrysocolaptes (l.) stricklandi, ‘Southern Sooty Woodpecker’ Mulleripicus (funebris) fuliginosus, Visayan Wattled Broadbill Eurylaimus (steerii) samarensis, White-lored Oriole Oriolus (steerii) albiloris, Tablas Drongo Dicrurus (hottentottus) menagei, Grand or Long-billed Rhabdornis Rhabdornis (inornatus) grandis, ‘Visayan Rhabdornis’ Rhabdornis (i.) rabori, and ‘Visayan Shama’ Copsychus (luzoniensis) superciliaris. -
Printable PDF Format
Field Guides Tour Report Thanksgiving in Jamaica 2019 Nov 24, 2019 to Nov 30, 2019 Cory Gregory & Dwane Swaby For our tour description, itinerary, past triplists, dates, fees, and more, please VISIT OUR TOUR PAGE. Jamaica has such a long list of amazingly beautiful and colorful birds that it's hard to pick a favorite. Close to the top of the list however surely was this Jamaican Spindalis, a species only found in Jamaica. Photo by guide Cory Gregory. Sitting between South America and Cuba, the Caribbean nation of Jamaica was a fantastic place for us to enjoy the warm weather, the plethora of unique and fascinating birds, the relaxed lifestyle, and escaping the holiday hustle and bustle. With the birdy and historical Green Castle Estate as our home base, we made a variety of daytrips and had the luxury of returning back to the same place every night! Our day trips took us to a variety of birding hotspots and between them all, we saw a vast majority of the avifauna that this island nation has to offer. Even in driving from Montego Bay to Green Castle on our first day, we were surrounded with attention-grabbing species like Magnificent Frigatebirds gliding overhead, Zenaida Doves sitting on the wires, and even a small gathering of the rare West Indian Whistling-Ducks in Discovery Bay! Our first day at Green Castle was our first foray into the forests and we quickly connected with a fun collection of endemic species like the showy Streamertail, Jamaican Woodpecker, Sad Flycatcher, White-chinned Thrush, Jamaican Spindalis, Orangequit, and many others. -
MADAGASCAR: the Wonders of the “8Th Continent” a Tropical Birding Custom Trip
MADAGASCAR: The Wonders of the “8th Continent” A Tropical Birding Custom Trip October 20—November 6, 2016 Guide: Ken Behrens All photos taken during this trip by Ken Behrens Annotated bird list by Jerry Connolly TOUR SUMMARY Madagascar has long been a core destination for Tropical Birding, and with the opening of a satellite office in the country several years ago, we further solidified our expertise in the “Eighth Continent.” This custom trip followed an itinerary similar to that of our main set-departure tour. Although this trip had a definite bird bias, it was really a general natural history tour. We took our time in observing and photographing whatever we could find, from lemurs to chameleons to bizarre invertebrates. Madagascar is rich in wonderful birds, and we enjoyed these to the fullest. But its mammals, reptiles, amphibians, and insects are just as wondrous and accessible, and a trip that ignored them would be sorely missing out. We also took time to enjoy the cultural riches of Madagascar, the small villages full of smiling children, the zebu carts which seem straight out of the Middle Ages, and the ingeniously engineered rice paddies. If you want to come to Madagascar and see it all… come with Tropical Birding! Madagascar is well known to pose some logistical challenges, especially in the form of the national airline Air Madagascar, but we enjoyed perfectly smooth sailing on this tour. We stayed in the most comfortable hotels available at each stop on the itinerary, including some that have just recently opened, and savored some remarkably good food, which many people rank as the best Madagascar Custom Tour October 20-November 6, 2016 they have ever had on any birding tour. -
Castle Green Bird List
GREEN CASTLE ESTATE Bird List Birds seen on recent tours during November – April | In one week we can expect around 120 species. E=Endemic | ES=Endemic Subspecies | I=Introduced Some of the species below are very unusual however they have been included for completeness. Jamaica has recorded over 300 species and the birds below are the most frequently encountered, however we cannot guarantee what we will or will not see, that’s birding! West Indian Whistling-Duck Lesser Yellowlegs Greater Antillean Elaenia (ES) Blue-winged Teal Whimbrel Jamaican Pewee (E) Northern Shoveler Ruddy Turnstone Sad Flycatcher (E) Ring-necked Duck Red Knot Rufous-tailed Flycatcher (E) Lesser Scaup Sanderling Stolid Flycatcher (ES) Masked Duck Semipalmated Sandpiper Gray Kingbird Ruddy Duck Western Sandpiper Loggerhead Kingbird (ES) Least Grebe Least Sandpiper Jamaican Becard (E) Pied-billed Grebe White-rumped Sandpiper Jamaican Vireo (E) White-tailed Tropicbird Baird's Sandpiper Blue Mountain Vireo (E) Magnificent Frigatebird Stilt Sandpiper Black-whiskered Vireo Brown Booby Short-billed Dowitcher Jamaican Crow (E) Brown Pelican Laughing Gull Caribbean Martin American Bittern Least Tern Tree Swallow Least Bittern Gull-billed Tern Northern Rough-winged Swallow Great Blue Heron Caspian Tern Cave Swallow (ES) Great Egret Royal Tern Barn Swallow Snowy Egret Sandwich Tern Rufous-throated Solitaire (ES) Little Blue Heron Rock Pigeon (I) White-eyed Thrush (E) Tricolored Heron White-crowned Pigeon White-chinned Thrush (E) Reddish Egret Plain Pigeon (ES) Gray Catbird Cattle -
Birding Madagascar 1-22 November 2018
Birding Madagascar 1-22 November 2018. Trip report compiled by Tomas Carlberg. 1 Front cover Daily log Red-capped Coua, sunbathing in Ankarafantsika National Park. Photo: Tomas Carlberg November 1st Some of us (TC, JN, and RN) flew Air France from Photos Arlanda, Stockholm at 06:00 to Paris, where we © All photos in this report: Tomas Carlberg. met OP (who flew from Gothenburg) and IF (flew For additional photos, see p. 30 ff. from Manchester). An 11 hrs flight took us to Antananarivo, where we landed just before Participants midnight. Once through after visa and passport control we met Zina at the airport. We stayed at IC Tomas Carlberg (Tour leader), Jonas Nordin, Hotel and fell asleep at 01:30. Sweden; Rolf Nordin, Sweden; Olof Persson, Sweden; Jesper Hornskov, Denmark; Eric November 2nd Schaumburg, Denmark; Hans Harrestrup Andersen, Woke up at 6, met the Danes (JH, ES, HW, and Denmark; Hans Wulffsberg, Denmark; Ian Fryer, UK HHA), and had breakfast. Changed c. 400 Euro each Serge “Zina” Raheritsiferana (organizer and driver), and got 1 540 000 ariary… Departure at 7:30 Fidson “Fidy” Albert Alberto (guide), and Lala. heading north towards Ankarafantsika NP. Saw a male Malagasy Harrier c. 16 km south of Ankazobe Correspondence (-18.45915, 47.160156), so stopped for birding [email protected] (Tomas Carlberg) there 9:45-10:05. Stop at 11:40 to buy sandwiches for lunch. Lunch with birding 12:55-13:15. Long Tour organizers transport today… Stopped for birding at bridge Serge “Zina” Raheritsiferana (Zina-Go Travel), over Betsiboka River 16:30-17:30; highlight here Stig Holmstedt. -
Congolius, a New Genus of African Reed Frog Endemic to The
www.nature.com/scientificreports OPEN Congolius, a new genus of African reed frog endemic to the central Congo: A potential case of convergent evolution Tadeáš Nečas1,2*, Gabriel Badjedjea3, Michal Vopálenský4 & Václav Gvoždík1,5* The reed frog genus Hyperolius (Afrobatrachia, Hyperoliidae) is a speciose genus containing over 140 species of mostly small to medium-sized frogs distributed in sub-Saharan Africa. Its high level of colour polymorphism, together with in anurans relatively rare sexual dichromatism, make systematic studies more difcult. As a result, the knowledge of the diversity and taxonomy of this genus is still limited. Hyperolius robustus known only from a handful of localities in rain forests of the central Congo Basin is one of the least known species. Here, we have used molecular methods for the frst time to study the phylogenetic position of this taxon, accompanied by an analysis of phenotype based on external (morphometric) and internal (osteological) morphological characters. Our phylogenetic results undoubtedly placed H. robustus out of Hyperolius into a common clade with sympatric Cryptothylax and West African Morerella. To prevent the uncovered paraphyly, we place H. robustus into a new genus, Congolius. The review of all available data suggests that the new genus is endemic to the central Congolian lowland rain forests. The analysis of phenotype underlined morphological similarity of the new genus to some Hyperolius species. This uniformity of body shape (including cranial shape) indicates that the two genera have either retained ancestral morphology or evolved through convergent evolution under similar ecological pressures in the African rain forests. African reed frogs, Hyperoliidae Laurent, 1943, are presently encompassing almost 230 species in 17 genera. -
Pseudoeurycea Naucampatepetl. the Cofre De Perote Salamander Is Endemic to the Sierra Madre Oriental of Eastern Mexico. This
Pseudoeurycea naucampatepetl. The Cofre de Perote salamander is endemic to the Sierra Madre Oriental of eastern Mexico. This relatively large salamander (reported to attain a total length of 150 mm) is recorded only from, “a narrow ridge extending east from Cofre de Perote and terminating [on] a small peak (Cerro Volcancillo) at the type locality,” in central Veracruz, at elevations from 2,500 to 3,000 m (Amphibian Species of the World website). Pseudoeurycea naucampatepetl has been assigned to the P. bellii complex of the P. bellii group (Raffaëlli 2007) and is considered most closely related to P. gigantea, a species endemic to the La specimens and has not been seen for 20 years, despite thorough surveys in 2003 and 2004 (EDGE; www.edgeofexistence.org), and thus it might be extinct. The habitat at the type locality (pine-oak forest with abundant bunch grass) lies within Lower Montane Wet Forest (Wilson and Johnson 2010; IUCN Red List website [accessed 21 April 2013]). The known specimens were “found beneath the surface of roadside banks” (www.edgeofexistence.org) along the road to Las Lajas Microwave Station, 15 kilometers (by road) south of Highway 140 from Las Vigas, Veracruz (Amphibian Species of the World website). This species is terrestrial and presumed to reproduce by direct development. Pseudoeurycea naucampatepetl is placed as number 89 in the top 100 Evolutionarily Distinct and Globally Endangered amphib- ians (EDGE; www.edgeofexistence.org). We calculated this animal’s EVS as 17, which is in the middle of the high vulnerability category (see text for explanation), and its IUCN status has been assessed as Critically Endangered. -
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. -
Efecto Del Huracán Jova En La Comunidad De Anfibios En Diferentes Estadios Sucesionales En Un Bosque Tropical Seco De Chamela, Jalisco, México
UNIVERSIDAD MICHOACANA DE SAN NICOLÁS DE HIDALGO FACULTAD DE BIOLOGIA Efecto del huracán Jova en la comunidad de anfibios en diferentes estadios sucesionales en un bosque tropical seco de Chamela, Jalisco, México Tesis Que presenta: Biol. Jorge Alejandro Marroquín Páramo Como requisito para obtener el título de: MAESTRO EN CIENCIAS EN ECOLOGÍA Y CONSERVACIÓN Director de tesis Maestro en Ciencias Bilógicas Javier Alvarado Díaz Morelia, Mich. Marzo de 2014. ÍNDICE CONTENIDO Pg. 1. Abstract ........................................................................................................................ 4 2. Resumen general .......................................................................................................... 5 3. Introducción ................................................................................................................ 7 4. CAPITULO I Efecto de los disturbios sobre la fauna silvestre. ............................ 10 4.1 Resumen .................................................................................................................... 10 4.2 Introducción .............................................................................................................. 11 4.3 Disturbios en escala de poblaciones .......................................................................... 12 4.4 Disturbios en escalas de comunidades y ecosistemas ............................................... 13 4.5 Respuesta de las comunidades al disturbio............................................................... -
Figs1 Speciestree Seqcap
Phrynomantis microps Microhylidae Breviceps adspersus Brevicipitidae Hemisus marmoratus Hemisotidae Leptopelis rufus Cardioglossa gracilis Arthtroleptis poecilinotus Leptodactylodon ovatus Arthroleptidae Nyctibates corrugatus Trichobatrachus robustus Scotobleps gabonicus Acanthixalus spinosus Acanthixalus sonjae Semnodactylus wealli Paracassina obscura Paracassina kounhiensis Kassininae Phlyctimantis maculata Phlyctimantis verrucosus Phlyctimantis boulengeri Phlyctimantis leonardi Kassina kuvangensis Kassina fusca Kassina lamottei Kassina senegalensis Kassina decorata Kassina maculosa Kassina arboricola Hyperoliidae Kassina cochranae Opisthothylax immaculatus Afrixalus enseticola Tachycnemis seychellensis Heterixalus luteostriatus Malagasy-Seychelles Heterixalus alboguttatus Species Afrixalus vibekensis Afrixalus weidholzi Afrixalus lacustris Afrixalus dorsimaculatus 1 Afrixalus dorsimaculatus 2 Afrixalus knysae Afrixalus spinifrons Hyperoliinae Afrixalus delicatus Afrixalus sylvaticus Afrixalus brachycnemis Afrixalus laevis Afrixalus lacteus Afrixalus fornasini Afrixalus wittei Afrixalus osorioi Afrixalus paradorsalis paradorsalis 2 Afrixalus paradorsalis paradorsalis 1 Afrixalus paradorsalis manengubensis Afrixalus nigeriensis Afrixalus vittiger 1 Afrixalus vittiger 2 Afrixalus dorsalis 3 Afrixalus dorsalis 1 Afrixalus quadrivittatus 1 Afrixalus quadrivittatus 2 Afrixalus dorsalis 2 Afrixalus fulvovittatus 2 Afrixalus fulvovittatus 1 Morerella cyanophthalma Cryptothylax greshoffii Hyperolius semidiscus Hyperolius parkeri Hyperolius