Observations on Nesting Noisy Pittas Pitta Versicolor

Total Page:16

File Type:pdf, Size:1020Kb

Observations on Nesting Noisy Pittas Pitta Versicolor VOL. 16 (1) MARCH 1995 Nesting Noisy Pittas 39 Adult male Noisy Pitta feeding nestlings at The Leap, Mackay, Queensland, during the nestling period December 1993/January 1994 Plate 12 Photo: Peter Taylor Observations on Nesting Noisy Pittas Pitta versicolor Little is known of the breeding behaviour of Australian pittas. Both sexes of the Noisy Pitta Pitta versicolor share incubation, which lasts 15 days; some aspects of display of the Noisy Pitta and Red-bellied Pitta P. erythrogaster have been described (Schodde & Tidemann 1986, Beruldsen 1990, Hobcroft 1992, Beruldsen & Uhlenhut 1995). Brief details of breeding behaviour in New Guinean pittas have also been obtained. Both sexes of the Red-bellied Pitta incubate/brood, and parental behaviour of the Hooded Pitta P. sordida has been described, in which the nestling period lasts c. 16 days (Coates 1990). This account describes the courtship, nesting, incubation and parental behaviour of a pair of Noisy Pittas during the period 22 November 1993 to 10 January 1994 at The Leap, Mackay, Queensland. The location and habitat were as previously described (Taylor 1994). The pair of Noisy Pittas built a nest in a bank wash-out of a dry, rocky creek, utilising a treated pine log on one side of the nest and the bank rock-face at the rear of the nest. The pine log supports an observation deck c. 10m from our house. Although they were very secretive, the birds accepted our presence and showed no fear of us. We made daily observations of the birds at their nest. We could not see into the nest clearly, but we did not attempt to inspect the interior closely for fear of causing desertion. During the early observations, we noted only two features that enabled us to separate the male from the female. The male had red undertail coverts, whereas the female's AUSTRALIAN 40 TAYLOR & TAYLOR BIRD WATCHER were more pink. The male's call was strong and assertive, whereas the female's was of a higher pitch and more hurried. Later, when they started feeding young, each parent used its own distinct flight path and observation perch before arrival at the nest. Before nesting, both birds were seen constantly in the immediate area of the nest site. During the day they searched for food on the forest floor, and in the evening roosted high in the trees. Once the nest was completed, the birds foraged much farther up the creek and were rarely seen foraging in the immediate area of the nest site. Courtship and mating During September 1993, the male Noisy Pitta became very vocal. Sometimes commencing as early as 0300 h, his calls continued throughout the day and evening. Finally a female answered. In the days following, both birds were seen together foraging and responding to each other's calls. Courting began in earnest with the female picking up a piece of debris from the forest floor and running along the ground with it. The male ran after her, she stopped and mating followed. Mating was witnessed twice, and on each occasion took place on the ground. The male emitted one short, single-note call immediately before mating, the only time that this call was heard. Nest and incubation The nest site was located on 22 November 1993 when the nest was almost complete. Both sexes shared in the construction. The nest was made of twigs, leaves, small roots, grasses and moss and seemed to have an area of 'matting' in front of the entrance. It was dome-shaped, the floor area raised at the entrance and falling back to the egg chamber. On the morning of 9 December, the female flew to the nest with nesting material in the usual manner. However, she went into the nest and did not reappear until late afternoon. On inspection, only two eggs were seen but the interior of the nest was dark; it is possible that a third egg was present. On the following day, the female's behaviour was repeated and four eggs had now been laid. Both sexes incubated the eggs. During the change-over procedure, the incoming bird called some distance from the nest. The sitting bird immediately flew out, thus leaving the incoming bird uninterrupted access. Soft nesting material was brought to the nest at most change­ overs. The length of the incubation stints varied in duration. Nestling period On Tl December 1993 a change in behavioural routine was noted. For the first and only time, both birds were seen together at the nest, the male feeding the female. Two eggs had hatched. Owing to the position of the nest and our reluctance to interfere at this crucial stage, it is not known whether all four eggs hatched but a maximum of two chicks was seen. Both parents fed the nestlings. A wide variety of food was collected, increasing in size as the chicks grew. Centipedes, grasshoppers, flies, ants, snails, caterpillars and earthworms were brought. In the afternoon of 10 January a change in parental feeding pattern was noted. The parents frequented the nest far less than previ9usly, aod did not pringas much food on each visit. The chicks were very vocal on the parents' arrival. This behaviour may have indicated that the chicks were about to leave the nest. The nestlings did not survive to fledging. A snake was seen eating one of the young at 2000 h on the evening of 10 January 1994. The other chick was dead in the nest. VOL. 16 (1) MARCH 1995 Nesting Noisy Pittas 41 The chicks were fully feathered and appeared to be the same size as the parents, with the pitta colours already apparent. Conclusion The incubation period lasted 17 days from the completion of the clutch, and the nestling period lasted 14 days to the point where fledging was imminent. These values, and the birds' parental behaviour and routines, are as previously reported for the Noisy Pitta or similar to these aspects of the nesting biology of other pittas (cf. Schodde . & Tidemann 1986, Coates 1990, Hobcroft 1992). References Beruldsen, G.R. (1990), 'Cape York in the Wet', Aust. Bird Watcher 13, 209-217. -- & Uhlenhut, K. (1995), 'Cape York in the Wet (Part Two)', Aust. Bird Watcher 16, 3-10. Coates, B.J. (1990), The Birds of Papua New Guinea, vol. 2, Dove, Brisbane. Hobcroft, D. (1992), 'The husbandry of the Noisy Pitta', Aust. A vi culture 46, 77-79. Schodde, R. & Tidemann, S.C. (Eds) (1986), Reader's Digest Complete Book of Australian Birds, 2nd edn, Reader's Digest Services, Sydney. Taylor, P. (1994), 'Observations on nesting White-browed Robins Poecilodryas superciliosa', Aust. Bird Watcher 15, 328-331. By PAT TAYLOR and PETER TAYLOR, 38 Sunrise Road, Tinbeerwah via Coo roy, Queensland 4563 Received 8 March 1994 • .
Recommended publications
  • Eurylaimides Species Tree
    Eurylaimides ⋆Velvet Asity, Philepitta castanea Schlegel’s Asity, Philepitta schlegeli ⋆ Philepittidae Common Sunbird-Asity, Neodrepanis coruscans Yellow-bellied Sunbird-Asity, Neodrepanis hypoxantha ⋆Grauer’s Broadbill, Pseudocalyptomena graueri ⋆Long-tailed Broadbill, Psarisomus dalhousiae ⋆ Eurylaimidae Dusky Broadbill, Corydon sumatranus Visayan Broadbill, Sarcophanops samarensis ⋆Wattled Broadbill, Sarcophanops steerii ⋆Silver-breasted Broadbill, Serilophus lunatus ⋆Black-and-red Broadbill, Cymbirhynchus macrorhynchos ⋆Banded Broadbill, Eurylaimus javanicus Black-and-yellow Broadbill, Eurylaimus ochromalus Gray-headed Broadbill, Smithornis sharpei Rufous-sided Broadbill, Smithornis rufolateralis Smithornithidae ⋆African Broadbill, Smithornis capensis Hose’s Broadbill, Calyptomena hosii ⋆Green Broadbill, Calyptomena viridis Calyptomenidae Whitehead’s Broadbill, Calyptomena whiteheadi ⋆Sapayoa, Sapayoa aenigma:0.1 Sapayoidae Blue-banded Pitta, Erythropitta arquata Garnet Pitta, Erythropitta granatina Graceful Pitta, Erythropitta venusta Black-crowned Pitta, Erythropitta ussheri Erythropitta Whiskered Pitta, Erythropitta kochi Philippine Pitta, Erythropitta erythrogaster Sula Pitta, Erythropitta dohertyi Sulawesi Pitta, Erythropitta celebensis Sangihe Pitta, Erythropitta caeruleitorques Siao Pitta, Erythropitta palliceps South Moluccan Pitta, Erythropitta rubrinucha North Moluccan Pitta, Erythropitta rufiventris Louisiade Pitta, Erythropitta meeki ⋆Papuan Pitta, Erythropitta macklotii Bismarck Pitta, Erythropitta novaehibernicae Pittidae
    [Show full text]
  • Chapter 02 Biogeography and Evolution in the Tropics
    Chapter 02 Biogeography and Evolution in the Tropics (a) (b) PLATE 2-1 (a) Coquerel’s Sifaka (Propithecus coquereli), a lemur species common to low-elevation, dry deciduous forests in Madagascar. (b) Ring-tailed lemurs (Lemur catta) are highly social. PowerPoint Tips (Refer to the Microsoft Help feature for specific questions about PowerPoint. Copyright The Princeton University Press. Permission required for reproduction or display. FIGURE 2-1 This map shows the major biogeographic regions of the world. Each is distinct from the others because each has various endemic groups of plants and animals. FIGURE 2-2 Wallace’s Line was originally developed by Alfred Russel Wallace based on the distribution of animal groups. Those typical of tropical Asia occur on the west side of the line; those typical of Australia and New Guinea occur on the east side of the line. FIGURE 2-3 Examples of animals found on either side of Wallace’s Line. West of the line, nearer tropical Asia, one 3 nds species such as (a) proboscis monkey (Nasalis larvatus), (b) 3 ying lizard (Draco sp.), (c) Bornean bristlehead (Pityriasis gymnocephala). East of the line one 3 nds such species as (d) yellow-crested cockatoo (Cacatua sulphurea), (e) various tree kangaroos (Dendrolagus sp.), and (f) spotted cuscus (Spilocuscus maculates). Some of these species are either threatened or endangered. PLATE 2-2 These vertebrate animals are each endemic to the Galápagos Islands, but each traces its ancestry to animals living in South America. (a) and (b) Galápagos tortoise (Geochelone nigra). These two images show (a) a saddle-shelled tortoise and (b) a dome-shelled tortoise.
    [Show full text]
  • Under the Canopy Worksheets
    Rainforest WORKSHEET 3 What is the importance of Dorrigo National Park? In the World Heritage symbol what do the circle and the square mean? Research link: http://whc.unesco.org/en/emblem/ Define rainforest by mentioning the canopy. What word describes the type of rainforest seen near the Rainforest Centre in the park? Name three reasons why this rainforest can grow at Dorrigo: 1. 2. 3. 1 Rainforest WORKSHEET 3 (CONTINUED) On the diagram below, label the following: • A buttress • An epiphyte • A mid-layer tree • A vine • The canopy layer • Ground ferns • An emergent tree • A herb Where do the plants living in the rainforest get their nutrients? 2 Rainforest WORKSHEET 3 (CONTINUED) Number the plants from the list of names and describe what strategies they use to No. grow in the dense, shady rainforest. 1. King orchid 2. Vines No. 3. Strangler fig No. 4. Cunjevoi lily 5. Pothos No. No. 3 Rainforest WORKSHEET 3 (CONTINUED) What roles do insects play in the rainforest? For each of the birds below, what layer of the forest do they live in and what food do they eat? Brush turkey noisy pitta topknot pigeon Name these animals which might be found in the rainforest. Which animal should not be there and why? 4 Rainforest WORKSHEET 3 (CONTINUED) How did Aboriginal people use rainforest? Describe in your own words how rainforest on Dorrigo Plateau was reduced to what now survives along the escarpment. What are some of the ways NSW National Parks and Wildlife Service tries to protect rainforest from visitor impacts? What other actions can be taken to conserve rainforest? 5.
    [Show full text]
  • Observations of Noisy Pitta Nestlings Through to Fledging
    Noisy Pitta nestlings The Whistler 11 (2017): 10-14 Observations of Noisy Pitta nestlings through to fledging Robert Kyte 22 Madison Drive, Adamstown Heights, NSW 2289, Australia. INTRODUCTION including Giant Stinging Tree Dendrocnide excelsa, Sydney Blue Gum Eucalyptus saligna, Turpentine The Noisy Pitta comprises two sub-species, Pitta Syncarpia glomulifera, Black Wattle Callicoma versicolor simillima which occurs in Northern serratifolia, Bollygum Neolitsea dealbata and Queensland and Pitta versicolor versicolor which is Rosewood Dysoxylum fraseranum with the found is southern Queensland and southward to the presence of Strangler Fig Ficus macrophylla. The Hunter River area of NSW and beyond. It is a mid and lower canopy includes Privet, Sandpaper colourful, ground-dwelling bird that spends its time Fig Ficus coronata, Lilli Pilli Acmena smithii, foraging for food on the forest floor. This very Blueberry Ash Elaeocarpus reticulates, Bangalow secretive bird is more often heard than seen with its Palm Archontophoenix cunninghamiana and lyrical call known as ‘walk-to-work’. It is listed as Cabbage Palm Livistona australis. Abundant ferns being of least concern by BirdLife International but include Gristle Fern Blechnum cartilagineum, may be diminishing in numbers due to habitat loss Rainbow Fern Culcita dubia and Giant Maiden Hair in the lowland regions of its autumn and winter Adiantum formosum. The forest floor is generally range (Cooper et al. 2014). Most records for the open, rich bare soil with decomposing leaf litter, Hunter Region come from higher altitude forested decomposing plant matter and scattered exposed gullies and rainforest areas where there are damp bedrock. conditions suitable for feeding or from lowland observations during winter months.
    [Show full text]
  • 5Th Grade Life Science: Ecosystems Unit
    5th Grade Life Science: Ecosystems Unit Developed for Chapel Hill Carrboro City Schools Northside Elementary School Outdoor Wonder & Learning (OWL) Initiative Unless otherwise noted, activities written by: Lauren Greene, Sarah Yelton, Dana Haine, & Toni Stadelman Center for Public Engagement with Science UNC Institute for the Environment In collaboration with 5th grade teachers at Northside Elementary School: Michelle Gay, Daila Patrick, & Elizabeth Symons ACKNOWLEDGEMENTS Many thanks to Dan Schnitzer, Coretta Sharpless, Kirtisha Jones and the many wonderful teachers and support staff at Northside Elementary for their participation in and support of the Northside OWL Initiative. Thanks also to Shelby Brown for her invaluable assistance compiling, editing, and proofreading the curriculum. Instructional materials and supplies to promote STEM-based outdoor learning were instrumental to the successful implementation of this curriculum. The purchase of these materials was made possible with funding provided by the Duke Energy Foundation to Chapel Hill-Carrboro City Schools. Curriculum developed June 2018 – July 2019 For more information, contact: Sarah Yelton, Environmental Education & Citizen Science Program Manager UNC Institute for the Environment Center for Public Engagement with Science [email protected] 5th Grade Ecosystems Unit Northside Outdoor Wonder & Learning Initiative Overarching Unit Question How and why do organisms (including humans) interact with their environment, and what are the effects of these interactions? Essential Questions Arc 1: How can I describe and compare different ecosystems? Arc 2: How is energy transferred through an ecosystem? How can I explain the interconnected relationships between organisms and their environments? Transfer Goals o Use scientific thinking to understand the relationships and complexities of the world around them.
    [Show full text]
  • 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.
    [Show full text]
  • Notes on the Diet of the Noisy Pitta Pitta Versicolor in New South Wales
    AUS'IRALIAN 42 BIRD WATCHER Notes on the Diet of the Noisy Pitta Pitta versicolor in New South Wales The diet of the Noisy Pitta Pitta versicolor consists of ground-dwelling invertebrates caught in damp places. Such prey includes insects, slaters, worms, and maggots taken from carrion; large forest snails, whose shells it breaks on anvils, are particularly favoured. It also takes berries and small fruits (Trudgeon 1971, Blakers et al. 1984, Schodde & Tidemann 1986, Strahan 1994). Species identified as prey include snails such as Helix, Hedleyella and Sphaerospira, centipedes, diplurans (Diplura, J apygidae ), beetles, grasshoppers, flies, ants, caterpillars and spiders (Barker & Vestjens 1990, Taylor & Taylor 1995, Totterman 1998). The diet of the similar Rainbow PittaP. iris includes skinks and the larvae of wood-boring beetles (Barker & Vestjens 1990). This note presents additional dietary data for the Noisy Pitta in New South Wales, from collections of snail shells at anvils at two sites, and the examination of the stomach contents of three dead specimens. The stomach contents were examined, microscopically if necessary, and identified by comparison with reference material. Snail shells were identified by the Malacology Department of the Australian Museum. 1 . St Ives, north of Sydney (33°42'S, 151°ll'E), 8 April1976 (p:r ABR): caught by a dog in a backyard that adjoined a wet sclerophyll gufly in Ku-ring-ga1 Chase National Park, and kept alive for three days before it died. Stomach empty, although fed earthworms while in care. Intestine contained the remains of earthworms (presumably reflecting the bird's diet while in captivity), spider (Araneae) and beetle (Coleoptera).
    [Show full text]
  • Final Report Prepared by WWF-Australia, Sydney NSW Cover Image: © Stephanie Todd / JCU / WWF-Aus a WWF-Australia Production
    1 Contents .............................................................................................. 2 Executive Summary ............................................................................ 4 Introduction ...................................................................................... 12 Objective 1. Estimate the current population status, distribution and habitat use of the northern bettong ................................................... 16 a) Population Status .................................................................................................................. 16 b) Population distribution ........................................................................................................ 24 c) Non-invasive conservation genetics ...................................................................................... 37 Objective 2. Assess the significance of the northern bettong's role in ecosystem function ........................................................................... 44 Objective 3. Develop appropriate fire management regimes for the northern bettong ............................................................................... 47 Key points ........................................................................................ 50 Discussion ......................................................................................... 52 Recommendations ............................................................................ 57 Publications .....................................................................................
    [Show full text]
  • Ornithological Literature of the Papuan Subregion 1915 to 1976 an Annotated Bibliography
    ORNITHOLOGICAL LITERATURE OF THE PAPUAN SUBREGION 1915 TO 1976 AN ANNOTATED BIBLIOGRAPHY CLIFFORD B. FRITH BULLETIN OF THE AMERICAN MUSEUM OF NATURAL HISTORY VOLUME 164 : ARTICLE 3 NEW YORK: 1979 4 ORNITHOLOGICAL LITERATURE OF THE PAPUAN SUBREGION 1915 TO 1976 AN ANNOTATED BIBLIOGRAPHY CLIFFORD B. FRITH Research Student, Monash University Melbourne, Australia BULLETIN OF THE AMERICAN MUSEUM OF NATURAL HISTORY VOLUME 164 : ARTICLE 3 NEW YORK: 1979 BULLETIN OF THE AMERICAN MUSEUM OF NATURAL HISTORY Volume 164, article 3, pages 377-465, figure 1 Issued September 21, 1979 Price: $6.15 a copy ISSN 0003-0090 Copyright (©) American Museum of Natural History 1979 INTRODUCTION "Bibliography is a most unrewarding occupation, because one tends to get blamed for what one has overlooked, rather than praised for what one has accomplished." (G. F. Mees, 1969) Compilation of this bibliography was origi- 1915) provides a historically noteworthy and a nally started for my personal reference and use suitable point of advancement in New Guinea as an aid to my ornithological work on the ornithology. It is particularly suitable because Papuan Subregion avifauna. The geographical Ogilvie-Grant provides in the introduction to area covered is that referred to by Mayr in his his account a list of over 175 "principal papers List of New Guinea Birds (1941) as the New relating to the birds of New Guinea; including Guinea Region, and subsequently termed the the Kei and Aru Islands," covering the years Papuan Subregion by Rand and Gilliard in their 1858-1915. This list provides a quick reference Handbook of New Guinea Birds (1967).
    [Show full text]
  • The State of Australia's Birds 2003
    T HE S TATE OF A USTRALIA’ S B IRDS 2003 Wedge-tailed Eagle. Photo by www.birdphotos.com.au JOIN TODAY! CONSERVATION THROUGH KNOWLEDGE By joining Birds Australia, you help Dedicated to the study, conservation and enjoyment of native birds Australia’s wild birds and their and their habitats habitats. Whether you participate Since 1901 Birds Australia (Royal Australasian Ornithologists Union) has in the activities and research or worked for the conservation of Australasia’s birds and their habitats, principally through just enjoy Australia’s leading bird scientific research. An independent, not-for- magazine Wingspan, your profit organisation, Birds Australia relies on the financial support of companies, trusts and subscription is hard at work, foundations, and private individuals. The organisation inspires the involvement of safeguarding our beautiful birds. thousands of volunteers in its conservation projects and through their generosity and commitment undertakes nationwide and Title First Name localised monitoring of bird populations. Surname 415 Riversdale Road, Hawthorn East, Victoria 3123 Address Tel: (03) 9882 2622; Fax: (03) 9882 2677; Postcode Email: [email protected] Phone (AH) (BH) Web site: www.birdsaustralia.com.au Email Funding for this report was generously provided by the Vera Moore Foundation Please accept my enclosed cheque for $68 $50 (concession) and the Australian Government’s $108 (family*) or $87 (family concession) payable to Department of Environment and Heritage (formerly Environment Australia). ‘Birds Australia’ or debit my Bankcard Visa Mastercard Vera Moore Foundation Expiry Date / Signature by Penny Olsen, Date / / SCIA.1 Michael Weston, Post to: Birds Australia, 415 Riversdale Rd, Hawthorn East, Vic.
    [Show full text]
  • Birding North Queensland, Australia by Keith and Kathryn Allen
    Birding North Queensland, Australia By Keith and Kathryn Allen Australia is the 6th largest country and its geographic isolation as the worlds’ largest island has resulted in the evolution of some very unique flora and fauna. For the visiting birdwatcher Australia has 828 extant species of birds with the attraction that 45% are endemic to this country. The problem is that one is faced with the logistics of planning a bird watching holiday in a country with such huge travelling distances and seasonal variations in weather. From our research we decided to concentrate on an area within the territory of North Queensland. This north-eastern tip of Australia has 59% of the extant bird species with a good number of endemics and has two of the top ten prime birding locations listed by Australian Geographic (Aug 04, 2011), namely the Atherton Tablelands and the tropical rainforests around Daintree. The geographic location of North Queensland also means it gets migrant and vagrant birds from South East Asia. Unfortunately, one of the star migrant birds, the Buff-breasted Paradise Kingfisher, arrives in North Queensland during the rainy season. With the aim of avoiding the hot /wet tropical climate we flew to Cairns via Singapore at the end of August for a 3 week holiday staying at Kuranda, Crater Lakes, Kingfisher Park and Daintree with a trip to the Barrier Reef before returning home. We arrived at Kuranda Birdwatchers’ Cabin with the owner greeting us by frantically waving her arms and telling us to remain in our car. The reason for this soon became apparent as two very large birds appeared that could very well have been props from the film Jurassic Park.
    [Show full text]
  • Husbandry Guidlines
    HUSBANDRY GUIDELINES FOR NOISY PITTA Pitta versicolor Captive Husbandry Guidelines for the Noisy Pitta Pitta versicolor 1 © Zoological Parks Board of NSW, February 2001 Introduction Noisy Pitta have a chequered history in captivity due to their complex pair bonding behaviour. Although longevity of individuals has in some instances been impressive for a passerine, at over 14 years (Taronga Zoo) a majority of specimens live less than 3 years. Pittas defend a territory aggressively and in captivity this frequently leads to the death of one animal during introduction or even within long standing pairings. Usually the female is the victim, but not exclusively. There are 3 sub species recognised for Noisy Pitta, however the captive management program is maintained at species level. The intention of this document is to highlight the husbandry challenges with this charismatic species and provide recommendations for their captive management. A majority of the information is based on Taronga Zoos extensive experience with Noisy Pitta, first displayed there in 1936. Common name: Noisy Pitta, also Dragon Bird, Buff Breasted Pitta Scientific Name: Pitta versicolor (Swainson, 1825) ASMP category: Management level 1b. O H & S Classification: Non Hazardous Band size: 8 Weights: 108.5g av, range 90- 140g (Taronga Zoo data. n = 35) Measurements 170-200mm Sexing method: No external dimorphism. It is recommended that juveniles be sexed at 3 months by laparoscopy or through DNA analysis using feathers. Captive Husbandry Guidelines for the Noisy Pitta Pitta versicolor 2 © Zoological Parks Board of NSW, February 2001 1. Taxonomy Class Aves Order Passeriformes Family Pittidae 2. Natural History 2.1 Morphometrics The most obvious being that Pittas are characterised, intalia, by their rounded wings and fully developed 10th (outermost) primary but 9 secondaries.
    [Show full text]