Description of the Nest, Eggs and Nestling Period of the Chestnut
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Biogeographic Regions and Events of Isolation and Diversification of the Endemic Biota of the Tropical Andes
Biogeographic regions and events of isolation and diversification of the endemic biota of the tropical Andes Nicolas A. Hazzia,b,1, Juan Sebastián Morenob, Carolina Ortiz-Movliavb,c, and Rubén Darío Palaciob,d aDepartment of Biological Sciences, The George Washington University, Washington, DC 20052; bFundación Ecotonos, Cali 76001000, Colombia; cFaculty of Mathematics and Natural Sciences, University of Bonn, 53115 Bonn, Germany; and dNicholas School of the Environment, Duke University, Durham, NC 27710 Edited by Nils Chr. Stenseth, University of Oslo, Oslo, Norway, and approved June 26, 2018 (received for review March 5, 2018) Understanding the spatial and temporal evolution of biota in the Eguiarte (14) hypothesized that the advance of ice sheets and tropicalAndesisamajorchallenge, given the region’s topographic páramo ecosystems during glacial maxima could have contracted complexity and high beta diversity. We used a network approach to humid montane species into refugia. These ideas notwithstanding, find biogeographic regions (bioregions) based on high-resolution spe- currently there is general agreement on the historical geography of cies distribution models for 151 endemic bird taxa. Then, we used dated the Andes and the origin of its biota, but it is the spatial and molecular phylogenies of 14 genera to reconstruct the area history temporal evolution within the region that has remained less clear through a sequence of allopatric speciation processes. We identified (12, 15). This task can be approached with the identification of 15 biogeographical regions and found 26 events of isolation and diver- areas that are characterized by distinct assemblages of living species, sification within their boundaries that are independently confirmed i.e., biogeographical regions (16). -
The Best of Costa Rica March 19–31, 2019
THE BEST OF COSTA RICA MARCH 19–31, 2019 Buffy-crowned Wood-Partridge © David Ascanio LEADERS: DAVID ASCANIO & MAURICIO CHINCHILLA LIST COMPILED BY: DAVID ASCANIO VICTOR EMANUEL NATURE TOURS, INC. 2525 WALLINGWOOD DRIVE, SUITE 1003 AUSTIN, TEXAS 78746 WWW.VENTBIRD.COM THE BEST OF COSTA RICA March 19–31, 2019 By David Ascanio Photo album: https://www.flickr.com/photos/davidascanio/albums/72157706650233041 It’s about 02:00 AM in San José, and we are listening to the widespread and ubiquitous Clay-colored Robin singing outside our hotel windows. Yet, it was still too early to experience the real explosion of bird song, which usually happens after dawn. Then, after 05:30 AM, the chorus started when a vocal Great Kiskadee broke the morning silence, followed by the scratchy notes of two Hoffmann´s Woodpeckers, a nesting pair of Inca Doves, the ascending and monotonous song of the Yellow-bellied Elaenia, and the cacophony of an (apparently!) engaged pair of Rufous-naped Wrens. This was indeed a warm welcome to magical Costa Rica! To complement the first morning of birding, two boreal migrants, Baltimore Orioles and a Tennessee Warbler, joined the bird feast just outside the hotel area. Broad-billed Motmot . Photo: D. Ascanio © Victor Emanuel Nature Tours 2 The Best of Costa Rica, 2019 After breakfast, we drove towards the volcanic ring of Costa Rica. Circling the slope of Poas volcano, we eventually reached the inspiring Bosque de Paz. With its hummingbird feeders and trails transecting a beautiful moss-covered forest, this lodge offered us the opportunity to see one of Costa Rica´s most difficult-to-see Grallaridae, the Scaled Antpitta. -
NOTES on COSTA RICAN BIRDS Time Most of the Marshes Dry up and Trees on Upland Sites Lose Their Leaves
SHORT COMMUNICATIONS NOTES ON COSTA RICAN BIRDS time most of the marshes dry up and trees on upland sites lose their leaves. In Costa Rica, this dry season GORDON H. ORIANS is known as “summer,” but in this paper we use the AND terms “winter” and “summer” to refer to winter and DENNIS R. PAULSON summer months of the North Temperate Zone. Department of Zoology Located in the lowland basin of the Rio Tempisque, University of Washington the Taboga region supports more mesic vegetation Seattle, Washington 98105 than the more elevated parts of Guanacaste Province. Originally the area must have been nearly covered The authors spent 29 June 1966 to 20 August 1967 with forest. In the river bottoms a tall, dense, largely in Costa Rica, primarily studying the ecology of Red- evergreen forest was probably the dominant vegetation. winged Blackbirds (Age&s phoeniceus) and insects The hillsides supported a primarily deciduous forest in the marshes of the seasonally dry lowlands of Guana- of lower stature. During the dry season the two caste Province. During this period many parts of the forest types are very different, with the hillside forests country were visited in exploratory trips for other pur- being exposed to extremes of temperature, wind, and poses. The Costa Rican avifauna is better known than desiccation and the bottomland forests retaining much that of any other tropical American country, thanks of their wet-season aspect. At present only scattered esoeciallv to the work of Slud ( 1964). This substantial remnants of the original forest remain, most of them fund of. -
Listing Five Foreign Bird Species in Colombia and Ecuador, South America, As Endangered Throughout Their Range; Final Rule
Vol. 78 Tuesday, No. 209 October 29, 2013 Part IV Department of the Interior Fish and Wildlife Service 50 CFR Part 17 Endangered and Threatened Wildlife and Plants; Listing Five Foreign Bird Species in Colombia and Ecuador, South America, as Endangered Throughout Their Range; Final Rule VerDate Mar<15>2010 18:44 Oct 28, 2013 Jkt 232001 PO 00000 Frm 00001 Fmt 4717 Sfmt 4717 E:\FR\FM\29OCR4.SGM 29OCR4 mstockstill on DSK4VPTVN1PROD with RULES4 64692 Federal Register / Vol. 78, No. 209 / Tuesday, October 29, 2013 / Rules and Regulations DEPARTMENT OF THE INTERIOR endangered or threatened we are proposed for these five foreign bird required to publish in the Federal species as endangered, following careful Fish and Wildlife Service Register a proposed rule to list the consideration of all comments we species and, within 1 year of received during the public comment 50 CFR Part 17 publication of the proposed rule, a final periods. rule to add the species to the Lists of [Docket No. FWS–R9–IA–2009–12; III. Costs and Benefits 4500030115] Endangered and Threatened Wildlife and Plants. On July 7, 2009, we We have not analyzed the costs or RIN 1018–AV75 published a proposed rule in which we benefits of this rulemaking action determined that the blue-billed because the Act precludes consideration Endangered and Threatened Wildlife curassow, brown-banded antpitta, Cauca of such impacts on listing and delisting and Plants; Listing Five Foreign Bird guan, gorgeted wood-quail, and determinations. Instead, listing and Species in Colombia and Ecuador, Esmeraldas woodstar currently face delisting decisions are based solely on South America, as Endangered numerous threats and warrant listing the best scientific and commercial Throughout Their Range under the Act as endangered species (74 information available regarding the AGENCY: Fish and Wildlife Service, FR 32308). -
First Report of the Nest and Young of the Variegated Antpitta (Grailaria
SHORT COMMUNICATIONS 499 SICK, H. 1985. Ornitologia Brasiliense, 2 ~01s. Editora Universidade de Brasilia, Brasilia, Brazil. SKUTCH, A. F. 1954. Life histories of Central American birds. Pacific Coast Avifauna 3 1: l-448. EDWIN 0. WILLIS, Dept. Zoologia, Univ. Estadual Paulista, 13.500 Rio Clara, Sao’ Paulo, Brazil. Received13 Aug. 1986, acceptedI I Feb. 1987. Wilson Bull., 99(3), 1987, pp. 499-500 First report of the nest and young of the Variegated Antpitta (Grallaria varia).-While conducting a study on microhabitat use by birds, I found a nest with two young of the Variegated Antpitta (Grulluria varia) 80 km north of Manaus, Amazonas, Brazil (225’ S,’ 595O’ W).’ I am unable to find any previously published description of the nest and young of this species. The nest was in upland forest about 25 m from an extensive area of 10-15- month-old second-growth, which had resulted from the clearing of the forest for cattle ranching. After the trees were cut, however, the area was abandoned. After the cutting, human activity had dropped to a minimum, except for an infrequently used trail that passed within 1 m of the nest. The nest was discovered 19 June 1984 by my field assistant, Jairo Miranda Lopes, on an upright <2-m rotting stump 40-50 cm in diameter. The nest, which was about 1.5 m above the ground, was a shallow cup 20 cm in diameter, lined with a thick mat of very small brown twigs and rootlets, and well concealed by a palm frond. The nest contained two young (eyes open, covered in black down, and spotted with brown juvenal feathers). -
Giant Antpitta Grallaria Gigantea
COTINGA 2 Giant Antpitta Giant Antpitta Grallaria gigantea N. Krabbe, G. DeSmet, P, Greenfield, M, Jácome, J. C. Matheus and F. Sornoza M. Introduction dawn, dusk, and during a rainy afternoon. One The Giant Antpitta inhabits the Andean slopes male was collected after being tape-recorded in Ecuador and southernmost Colombia. It (Krabbe). They were heard in a ravine, on the had only been found at a few sites where habi steep slopes that were covered with wet mossy tat destruction was known to be advanced, and forest, and were observed 1–3 m above the the latest verified record of the species dated ground in patches of mossy understorey, in from 1958. All three subspecies, namely cluding bamboo. The stomach contained an 6.5 gigantea, lehmanni and hylodroma were there cm long, strongly sclerotized, platyform, black- fore treated as globally threatened by Collar and-yellow-striped scarabaeid beetle larva. On et al.1, who published all available informa 3 December 1993 and 12 February 1994 tion on the species. Since then data on its song, Matheus observed a Giant Antpitta crossing habitat and diet have been obtained. The new a track at 1,320 m, 3.1 km south-east of Mindo records, all from Ecuador, are detailed below. (0°04'S 78°45'W), in the c.100 m wide plain of North-western slope of Volcán Pichincha Rio Mindo. Both slopes were covered by wet, (hylodroma): mossy forest, but the plain had only patches In early November 1991 Greenfield tape-re of secondary, though still somewhat moss-cov corded what he suspected to be Giant ered, vegetation. -
Description of the Nest, Egg and Nestling of Watkins's Antpitta
Cotinga 21 Description of the nest, egg and nestling of Watkins’s Antpitta Grallaria watkinsi Paul R. Martin and Robert C. Dobbs Cotinga 21 (2004): 35–37 Describimos el nido, huevos y pichón de la Gralaria de Watkins Grallaria watkinsi en base a observaciones hechas cerca de Celica, Loja, Ecuador, a principios de marzo de 2000. El nido, único entre los previamente descriptos para gralarias, estaba localizado relativamente alto en un árbol, apoyado en ramas pequeñas, y estaba compuesto principalmente de palitos. El huevo era azul verdoso pálido y sin marcas, similar a los huevos conocidos de otras especies de Grallaria. Como ya fuera mencionado para otros pichones del género, la G. watkinsi de 1–2 días de edad tenía el pico, comisura e interior de la boca anaranjado brillantes, pero resultó única en tener también la cloaca de ese color. Watkins’s Antpitta Grallaria watkinsi is a poorly cup depth was 5 cm and the external nest height known species largely restricted to the Tumbesian (i.e. bottom of the nest proper to the rim of the cup) region of south-west Ecuador and north-west Peru8, was 10 cm, with an additional 7 cm of woody where it inhabits tropical deciduous forest at 600– material hanging below. 2,000 m1,6. Although G. watkinsi was formerly considered a subspecies of Chestnut-crowned Egg description Antpitta G. ruficapilla, the two are vocally distinct5,6 The unhatched egg measured 30.09 x 25.33 mm and largely segregated by habitat and elevation8. and had a short subelliptical shape. Its mass was G. -
'Abnormal' Clutches of Scaled Antpitta Grallaria
Cotinga 38 Short Communications Tw of Graaia gatiani Published descriptions of Grallaria (Grallariidae) eggs are all relatively consistent, usually described as some shade of blue, with few or no 7 markings . Scaled Antpitta G. 8 guatimalensis is no exception , with the following published records: pale blue (nominate5,6); deep blue or ‘robin’s-egg blue’ (G. g. ochraceiventris18; nominate19); 24 22 blue-green (nominate ; ssp.? ); turquoise-blue (G. g. regulus3,4); or simply blue (ssp.?17). Rowley’s18,19 eggs were described as ‘bluish’ 98 Cotinga 38 Short Communications cup was 14 cm tall, but only 3.5 cm tall at the upper end. Overall external diameter was 22 cm, with the overhanging portions being supported by epiphytic vegetation. The internal measurements of the cup were 9.5 wide by 6.5 deep. The bulky cup was formed primarily of humid leaves and small sticks, with a rather loose internal cup of dark rootlets. Apart from the white eggs, the nests described here are largely similar to those described from elsewhere in the species’ range7,8. Naturalists have been puzzled by the widespread occurrence of blue-pigmented eggs across the avian phylogeny for many years, especially given their apparent obviousness to predators. Adaptive hypotheses for blue eggs proposed in the past include thermoregulation1, aposematism23, crypsis12 and egg recognition20. One relatively new hypothesis that has acquired some support, is sexual- signaling hypothesis9,15, which postulates that egg coloration is a reliable signal of female quality because the pigments responsible for blue-green shell pigments (biliverdins) are valuable antioxidents11, and only healthy females should be able to afford iur st an s o Sca ntitta Grallaria guatimalensis in southst to include biliverdins in their cuaor shoin immacuat hit s aro rn eggshells during the stressful process of egg formation. -
The Avifauna of the Matura Environmentally Sensitive Area, Trinidad and Tobago
The Avifauna of the Matura Environmentally Sensitive Area, Trinidad and Tobago Graham White, Kevin Mahabir, Mike Oatham and Courtenay Rooks White, G., Mahabir, K., Oatham, M., and Rooks, C. 2015. The Avifauna of the Matura Environmentally Sensitive Area, Trinidad and Tobago. Living World, Journal of The Trinidad and Tobago Field Naturalists’ Club , 2015, 23-36. The Avifauna of the Matura Environmentally Sensitive Area, Trinidad and Tobago Graham White1, Kevin Mahabir2, Mike Oatham2 and Courtenay Rooks3 1. [email protected] 2. Department of Life Sciences, University of the West Indies, St. Augustine. 3DULD6SULQJV(FR&RPPXQLW\%UDVVR6HFR ABSTRACT A baseline survey of the avifauna of the Matura Environmentally Sensitive Area (MESA) in Trinidad was conducted to characterise the avifauna of the site and establish the presence of species of particular conservation interest. Surveys were conducted over 22 days on nine site visits between 2008 and 2010 from 152 sector (transect) surveys, supplement- ed by general observation. Overall, 95 species and 1067 individuals were detected, including 89 year-round residents, three non-breeding migrants, and three species which breed locally but disperse post breeding to the mainland. This represents 59% of the species expected in the MESA. The rate of species accumulation suggests that further sampling ZLOO\LHOGRQHDGGLWLRQDOVSHFLHVSHUWHQVHFWRUV7KHDVVHPEODJHVREVHUYHGUHÀHFW7ULQLGDG¶VSUR[LPLW\WR6RXWK$PHULFD %RWKRI7ULQLGDG¶VHQGHPLFELUGVWKH7ULQLGDG0RWPRWMomotus bahamensis, Trinidad Piping-Guan, Pipile pipile, and the rare Scaled Antpitta, Grallaria guatimalensis, were detected within the study area. High-altitude specialists observed include the Brown Violetear, Colibri delphinae, Speckled Tanager, Tangara guttata, Hepatic Tanager, Piranga ÀaYa and Yellow-legged Thrush, Turdus ÀaYipes. The vegetation and altitude along the trail across the MESA on which the survey ZDVFRQGXFWHGLVGHVFULEHGLQVHFWLRQV7KHGHJUHHRIGLI¿FXOW\DQGSRWHQWLDOFDPSLQJORFDWLRQVRIHDFKVHFWLRQDUHDOVR described to facilitate subsequent surveys. -
Field Notes on the Giant Antpitta Grallaria Gigantea
COTINGA 7 Field notes on the G iant A ntpitta G rallaria gigantea Y. de Soye, K.-L. Schuchmann and J. C. Matheus Se presentan nuevas observaciones de Grallaria gigantea del sudoeste Colombiano y noroeste de Ecuador. Dos registros visuales, de subespecie desconocida, fueron efectuados en la Reserva La Planada, Depto. Nariño, Colombia en 1988 y 1989, y uno, de la subespecie hylodroma, fue atrapado en Mindo, provincia de Pichincha, Ecuador en 1994. Se presenta la biometría de este individuo y se describe el comportamiento alimentar de otros observados en el campo, en Mindo. Aparentemente se alimentaban de lombrices Rhynodrylus y otros invertebrados. Hasta 3–4 G. gigantea fueron escuchados en el área de Mindo en noviembre–diciembre 1994. The Giant Antpitta Grallaria gigantea is reported recorded weight does not confirm the statement to inhabit forests of the Andean slopes of Ecuador by Krabbe et al.3 th at “gigantea differs from and southernmost Colombia. Three subspecies are hylodroma by its larger size”, with their two speci recognised: Colombian lehmanni, west Ecuadorian mens weighing 266 g and 218 g. Their sample was hylodroma and east Ecuadorian nominate evidently too small to distinguish subspecific dif gigantea3, with given localities separated by large ferences. distances. Most information available on biology Both at La Planada and near Mindo, foraging and distribution of this rarely encountered bird is individuals of Grallaria gigantea were observed on presented by Collar et al.1 and Krabbe et al . The several occasions. At La Planada, a bird was seen conservation status of the species was ranked as along a trail feeding on slugs. -
On the Origin and Evolution of Nest Building by Passerine Birds’
T H E C 0 N D 0 R r : : ,‘ “; i‘ . .. \ :i A JOURNAL OF AVIAN BIOLOGY ,I : Volume 99 Number 2 ’ I _ pg$$ij ,- The Condor 99~253-270 D The Cooper Ornithological Society 1997 ON THE ORIGIN AND EVOLUTION OF NEST BUILDING BY PASSERINE BIRDS’ NICHOLAS E. COLLIAS Departmentof Biology, Universityof California, Los Angeles, CA 90024-1606 Abstract. The object of this review is to relate nest-buildingbehavior to the origin and early evolution of passerinebirds (Order Passeriformes).I present evidence for the hypoth- esis that the combinationof small body size and the ability to place a constructednest where the bird chooses,helped make possiblea vast amountof adaptiveradiation. A great diversity of potential habitats especially accessibleto small birds was created in the late Tertiary by global climatic changes and by the continuing great evolutionary expansion of flowering plants and insects.Cavity or hole nests(in ground or tree), open-cupnests (outside of holes), and domed nests (with a constructedroof) were all present very early in evolution of the Passeriformes,as indicated by the presenceof all three of these basic nest types among the most primitive families of living passerinebirds. Secondary specializationsof these basic nest types are illustratedin the largest and most successfulfamilies of suboscinebirds. Nest site and nest form and structureoften help characterizethe genus, as is exemplified in the suboscinesby the ovenbirds(Furnariidae), a large family that builds among the most diverse nests of any family of birds. The domed nest is much more common among passerinesthan in non-passerines,and it is especially frequent among the very smallestpasserine birds the world over. -
Trinidad & Tobago
Victor Emanuel Nature Tours TRINIDAD & TOBAGO 24 February – 4 March, 2007 Caribbean Martin Progne dominicensis Leader: David Ascanio Compiled by: David Ascanio Victor Emanuel Nature Tours, inc. 2525 Wallington Drive, Suite 1003 Austin, TX 78746 www.ventbird.com Victor Emanuel Nature Tours Trinidad & Tobago February 23 – March 4, 2007 Leader: David Ascanio In January 22nd I was leading a VENT Cruise in the Peruvian Amazon, when I received a radio message from Lima. Bob Sudstron, my VENT colleague could not lead the Trinidad and Tobago tour next February, and they needed to know if I could take over his position. As I was hearing the message, a memory came about my last time in Tobago. I believe it may have been more that ten years ago, I thought, when I accompanied Richard ffrench, the author of the Trinidad and Tobago bird book into this fascinating country. Trinidad and Tobago comprises two islands. Tobago, with a population of about fifty thousand people, and the much larger Trinidad, with over a million inhabitants. Being small, this country represents indeed one of the best introductions to bird South America with many neotropical families represented but not an overwhelming number of species. We met at Piarco airport in Port of Spain to catch our flight to Tobago. After a drive to Cuffie river nature retreat we started birding with scope views of White- tailed Nightjar while a Common Potto called some distance away. In the following day we explored what is claimed to be the first protected forest in the western hemisphere (1765) in the Gilpin Trace.