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A 'Slow Pace of Life' in Australian Old-Endemic Passerine Birds Is Not Accompanied by Low Basal Metabolic Rates
University of Wollongong Research Online Faculty of Science, Medicine and Health - Papers: part A Faculty of Science, Medicine and Health 1-1-2016 A 'slow pace of life' in Australian old-endemic passerine birds is not accompanied by low basal metabolic rates Claus Bech University of Wollongong Mark A. Chappell University of Wollongong, [email protected] Lee B. Astheimer University of Wollongong, [email protected] Gustavo A. Londoño Universidad Icesi William A. Buttemer University of Wollongong, [email protected] Follow this and additional works at: https://ro.uow.edu.au/smhpapers Part of the Medicine and Health Sciences Commons, and the Social and Behavioral Sciences Commons Recommended Citation Bech, Claus; Chappell, Mark A.; Astheimer, Lee B.; Londoño, Gustavo A.; and Buttemer, William A., "A 'slow pace of life' in Australian old-endemic passerine birds is not accompanied by low basal metabolic rates" (2016). Faculty of Science, Medicine and Health - Papers: part A. 3841. https://ro.uow.edu.au/smhpapers/3841 Research Online is the open access institutional repository for the University of Wollongong. For further information contact the UOW Library: [email protected] A 'slow pace of life' in Australian old-endemic passerine birds is not accompanied by low basal metabolic rates Abstract Life history theory suggests that species experiencing high extrinsic mortality rates allocate more resources toward reproduction relative to self-maintenance and reach maturity earlier ('fast pace of life') than those having greater life expectancy and reproducing at a lower rate ('slow pace of life'). Among birds, many studies have shown that tropical species have a slower pace of life than temperate-breeding species. -
DRAFT Biodiversity Action Plan 2021 - 2026
DRAFT Biodiversity Action Plan 2021 - 2026 Prepared by: Infrastructure Services & Planning and Ecology Australia Contents Acknowledgments 4 A Vision for the Future 5 Introduction 6 Summary of state and extent of biodiversity in Greater Dandenong 7 Study area 7 Flora and fauna 9 Existing landscape habitat types 10 Key threats to local biodiversity values 12 Habitat assessments 15 Habitat connectivity for icon species 16 Community consultation and engagement 18 Biodiversity legislation considerations 20 Council strategies 22 Actions 23 Protection and enhancement of existing biodiversity values 24 Improving knowledge of biodiversity values 26 Facilitating and encouraging biodiversity conservation and enhancement on private land 27 Managing threatening processes 28 Community engagement and education 30 References 32 Tables Table 1 Summary of most common reasons why biodiversity is considered important from online survey and examples of comments provided 19 Table 2 Commonwealth and Victorian biodiversity legislation 20 Plates Plate 1 City of Greater Dandenong LGA and municipality study area, including surrounding areas of biodiversity significance. 8 Plate 2 Potential connectivity sites within Greater Dandenong for all five icon species 17 DRAFT City of Greater Dandenong Biodiversity Action Plan 2021 – 2026 ii Appendices Appendix 1 Vegetation coverage across the City of Greater Dandenong pre 1750 (left) and today (right). 34 Appendix 2 Fauna species listed as threatened under the EPBC Act 1999 (DAWE 2020), FFG Act 1988 (DELWP 2019b) or the Victorian Threatened Species Advisory List recorded within the City of Greater Dandenong municipality ....................................................................................................... 35 Appendix 3 Flora species listed as threatened under the EPBC Act 1999 (DAWE 2020), FFG Act 1988 (DELWP 2019b) or the Victorian Threatened Species Advisory List recorded within the City of Greater Dandenong municipality ...................................................................................................... -
Regent Honeyeater Identification Guide
REGENT HONEYEATER IDENTIFICATION GUIDE Broad patch of bare warty Males call prominently, skin around the eye, which whereas females only is smaller in young birds occasionally make soft calls. and females. Best seen at close range or with binoculars. Plumage around the head Regent Honeyeaters are and neck is solid black 20-24 cm long, with females giving a slightly hooded smaller and having duller appearance. plumage than the males. Distinctive scalloped (not streaked) breast. Broad stripes of yellow in the wing when folded, and very prominent in flight. From below the tail is a bright yellow. From behind it’s black bordered by bright yellow feathers. COMMON MISIDENTIFICATIONS YELLOW-TUFTED HONEYEATER NEW HOLLAND HONEYEATER WHITE-CHEEKED HONEYEATER Lichenostomus melanops Phylidonyris novaehollandiae Phylidonyris niger Habitat: Box-Gum-Ironbark Habitat: Woodland with heathy Habitat: Heathlands, parks and woodlands and forest with a understorey, gardens and gardens, less commonly open shrubby understorey. parklands. woodland. Notes: Common, sedentary bird Notes: Often misidentified as a Notes: Similar to New Holland of temperate woodlands. Has a Regent Honeyeater; commonly Honeyeaters, but have a large distinctive yellow crown and ear seen in urban parks and gardens. patch of white feathers in their tuft in a black face, with a bright Distinctive white breast with black cheek and a dark eye (no white yellow throat. Underparts are streaks, several patches of white eye ring). Also have white breast plain dirty yellow, upperparts around the face, and a white eye streaked black. olive-green. ring. Tend to be in small, noisy and aggressive flocks. PAINTED HONEYEATER CRESCENT HONEYEATER Grantiella picta Phylidonyris pyrrhopterus Habitat: Box-Ironbark woodland, Habitat: Wetter habitats like particularly with fruiting mistletoe forest, dense woodland and Notes: A seasonal migrant, only coastal heathlands. -
Download Preprint
A continental measure of urbanness predicts avian response to local urbanization Corey T. Callaghan*1 (0000-0003-0415-2709), Richard E. Major1,2 (0000-0002-1334-9864), William K. Cornwell1,3 (0000-0003-4080-4073), Alistair G. B. Poore3 (0000-0002-3560- 3659), John H. Wilshire1, Mitchell B. Lyons1 (0000-0003-3960-3522) 1Centre for Ecosystem Science; School of Biological, Earth and Environmental Sciences; UNSW Sydney, Sydney, NSW, Australia 2Australian Museum Research Institute, Australian Museum, Sydney, NSW, Australia, 3Evolution and Ecology Research Centre; School of Biological, Earth and Environmental Sciences; UNSW Sydney, Sydney, NSW, Australia *Corresponding author: [email protected] NOTE: This is a pre-print, and the final published version of this manuscript can be found here: https://doi.org/10.1111/ecog.04863 Acknowledgements Funding for this work was provided by the Australian Wildlife Society. Mark Ley, Simon Gorta, and Max Breckenridge were instrumental in conducting surveys in the Blue Mountains. We also are grateful to the numerous volunteers who submit their data to eBird, and the dedicated team of reviewers who ensure the quality of the database. We thank the associate editor and two anonymous reviewers for comments that improved this manuscript. Author contributions CTC, WKC, JHW, and REM conceptualized the data processing to assign urban scores. CTC, MBL, and REM designed the study. CTC performed the data analysis with insight from WKC and AGBP. All authors contributed to drafting and editing the manuscript. Data accessibility Code and data necessary to reproduce these analyses have been uploaded as supplementary material alongside this manuscript, and will be made available as a permanently archived Zenodo repository upon acceptance of the manuscript. -
Accepted Version
ACCEPTED VERSION Patrick L. Taggart Are blood haemoglobin concentrations a reliable indicator of parasitism and individual condition in New Holland honeyeaters (Phylidonyris novaehollandiae)? Transactions of the Royal Society of South Australia, 2016; 140(1):17-27 © 2016 Royal Society of South Australia "This is an Accepted Manuscript of an article published by Taylor & Francis in Transactions of the Royal Society of South Australia on 01 Mar 2016 available online: http://dx.doi.org/10.1080/03721426.2016.1151970 PERMISSIONS http://authorservices.taylorandfrancis.com/sharing-your-work/ Accepted Manuscript (AM) As a Taylor & Francis author, you can post your Accepted Manuscript (AM) on your personal website at any point after publication of your article (this includes posting to Facebook, Google groups, and LinkedIn, and linking from Twitter). To encourage citation of your work we recommend that you insert a link from your posted AM to the published article on Taylor & Francis Online with the following text: “This is an Accepted Manuscript of an article published by Taylor & Francis in [JOURNAL TITLE] on [date of publication], available online: http://www.tandfonline.com/[Article DOI].” For example: “This is an Accepted Manuscript of an article published by Taylor & Francis Group in Africa Review on 17/04/2014, available online:http://www.tandfonline.com/10.1080/12345678.1234.123456. N.B. Using a real DOI will form a link to the Version of Record on Taylor & Francis Online. The AM is defined by the National Information Standards Organization as: “The version of a journal article that has been accepted for publication in a journal.” This means the version that has been through peer review and been accepted by a journal editor. -
Build a Bee Home in Your Backyard Australia Has Over 2,000 Solitary Bee Species Needing Homes
Support the Pollinator Link® project Build a Bee Home in your backyard Australia has over 2,000 solitary bee species needing homes. DIY Projects Hives of small black Stingless Native Bees Tetragonula sp. have become popular in urban backyards and are increasingly important for pollination M. Fox of agricultural crops like Queensland Nuts Macadamia integrifolia. Less well known are the 2,000 species of native solitary bees: species diversity provides pollination security by reducing risks from species specific disease. Some species: Blue Banded Bees, Teddy Bear Bees and Carpenter Bees also provide a special type of pollination service called Buzz Pollination – shaking pollen out by vibrating flowers with strong wing muscles or head banging the flowers. Buzz Pollination is particularly valuable for the tomatoes, kiwi fruit, eggplants, blueberries, cranberries and chilli peppers, in your backyard vegetable garden. The European Honey Bee Apis mellifera cannot perform Buzz Pollination. Stingless native bee hive Solitary native bees come in a wide range of colours: bright orange furry Teddy A. Moore Bear Bees and shiny green Metallic Carpenter Bees; and sizes, from 12mm Blue Banded Bees to the huge loud 24mm Great Carpenter Bees. Adult solitary native bee generally only fly during the warm months and die before winter. Immature bees remain sealed in their cells inside the nests during the winter. They develop into adults and emerge in spring when the warm weather returns and your plants need pollinators. Solitary bee nests: Many solitary bees nest in burrows in the ground while others Teddy Bear Bee nest in pre-existing crevices or holes in timber. -
December 2016 Vol
Castlemaine Naturalist December 2016 Vol. 41.11 #449 Monthly newsletter of the Castlemaine Field Naturalists Club Inc. Powerful Owl chick - photo Noel Young Moths of Victoria – and Castlemaine CFNC members were fortunate to have Marilyn Hewish as guest speaker at the Club’s November meeting. Marilyn is a distinguished naturalist, who received the Australian Natural History Medallion in 2013 for her decades of work on Australian birds and her more recent contributions to studies of the moths of Victoria. She told us how she had become a “moth addict” and that most of the commonly stated ways to distinguish moths and butterflies are myths – some moths are active during daylight, many are highly coloured (not “brown and boring”), some have clubbed antennae. The technical difference is in the way the forewings and hindwings are linked – needing microscopic examination! Moths and their caterpillars play a major ecological role, for example as a significant food source for birds, bats, reptiles, small mammals and larger invertebrates. Some caterpillars feed on leaf litter, thus recycling nutrients and reducing the intensity of fires. Some day-flying moths pollinate flowers. Though butterflies are more familiar to most naturalists, they are far outnumbered by moth species in Australia: about 400 species of butterflies and more than 20,000 moths (the exact figure is not known). The studies of Victorian moths are in very early stages compared to our knowledge of Australian birds. Marilyn and Dean are frequently in the field – at night (even when cold and wet), surveying moths at sites across Victoria. They often record large extensions in distributions, species not previously known from the state, and even species new to science. -
Downloadfile/616075 Toft, J
REVIEW published: 30 April 2021 doi: 10.3389/fevo.2021.582041 Designing (for) Urban Food Webs Alexander J. Felson 1,2,3 and Aaron M. Ellison 4* 1 Melbourne School of Design, Faculty of Architecture, Building and Planning, University of Melbourne, Melbourne, VIC, Australia, 2 Connecticut Institute for Resilience and Climate Adaptation, University of Connecticut, Groton, CT, United States, 3 Urban Ecology and Design Lab and Ecopolitan Design, New Haven, CT, United States, 4 Harvard Forest, Harvard University, Petersham, MA, United States Interest is growing in designing resilient and ecologically rich urban environments that provide social and ecological benefits. Regenerative and biocentric designs fostering urban ecological habitats including food webs that provide ecosystem services for people and wildlife increasingly are being sought. However, the intentional design of urban landscapes for food webs remains in an early stage with few precedents and many challenges. In this paper, we explore the potential to design (for) urban food webs through collaborations between designers and ecologists. We start by examining the ecology and management of Jamaica Bay in New York City as a case study of an anthropogenic landscape where ecosystems are degraded and the integrity of extant food webs are intertwined with human agency. A subsequent design competition focusing on ecological design and management of this large-scale landscape for animal habitat and ecosystem Edited by: services for people illustrates how designers approach this anthropogenic landscape. Mary L. Cadenasso, This case study reveals that both designing urban landscapes for food webs and directly University of California, Davis, United States designing and manipulating urban food webs are complicated and challenging to achieve Reviewed by: and maintain, but they have the potential to increase ecological health of, and enhance Frederick R. -
Planting and Creating Habitat Toattract Bees
Bee Walls Bee Gardens Bee Habitat Bee Trees Planting and Creating Habitat toAttract Bees BLUE-BANDED SOLITARY DIANNE BY CLARKE Conserving all bees : for the health of our environment and on-going food supply Gardeners can choose a wide variety of plants to attract and support bees. Floral embrace! Some plants provide valuable supplies of nectar and pollen for the bees whilst PHOTO BOB LUttRELL others assist the bees with their nest building. Native plants are usually best for native bees, and can be used in both wild areas and gardens. There are also many garden plants - particularly heirloom varieties of perennials and herbs - that are good sources of nectar or pollen. Together with native plants, these will make a garden attractive to both pollinators and people. The need... The need for this document arose from our Valley Bees meetings. Members enquired about habitat that could be of benefit to all bees, what trees and plants to conserve and plant on their properties, how to attract pollinators to our gardens, and (for those who What is pollen? had bees as an activity) when did these plants produce nectar and pollen to provide food for bees. Pollen is the male component of the reproductive cycle of flowering A call was put out for a survey, and the knowledge of people experienced in the field was collected and collated to provide this survey of the trees in the local Mary River Catchment area. plants. It is produced in the anthers of the flowers. For fruit and seeds to We thank Ernie Rider, Kayle Findlay, Roy Barnes, Norm Salt and Pauline Alexander for their valuable form, the pollen must be transferred to the stigma to enter the ovaries. -
The Signal Environment Is More Important Than Diet Or Chemical Specialization in the Evolution of Warning Coloration
The signal environment is more important than diet or chemical specialization in the evolution of warning coloration Kathleen L. Prudic†‡, Jeffrey C. Oliver§, and Felix A. H. Sperling¶ †Department of Ecology and Evolutionary Biology and §Interdisciplinary Program in Insect Science, University of Arizona, Tucson, AZ 85721; and ¶Department of Biological Sciences, University of Alberta, Edmonton, AB, Canada T6G 2E9 Edited by May R. Berenbaum, University of Illinois at Urbana–Champaign, Urbana, IL, and approved October 11, 2007 (received for review June 13, 2007) Aposematic coloration, or warning coloration, is a visual signal that in ref. 13). Prey can become noxious by consuming other organisms acts to minimize contact between predator and unprofitable prey. with defensive compounds (e.g., refs. 15 and 16). By specializing on The conditions favoring the evolution of aposematic coloration re- a particular toxic diet, the consumer becomes noxious and more main largely unidentified. Recent work suggests that diet specializa- likely to evolve aposematic coloration as a defensive strategy tion and resultant toxicity may play a role in facilitating the evolution (reviewed in ref. 13). Diet specialization, in which a consumer feeds and persistence of warning coloration. Using a phylogenetic ap- on a limited set of related organisms, allows the consumer to tailor proach, we investigated the evolution of larval warning coloration in its metabolism to efficiently capitalize on the specific toxins shared the genus Papilio (Lepidoptera: Papilionidae). Our results indicate that by a suite of related hosts. Recent investigations suggest that diet there are at least four independent origins of aposematic larval specialization on toxic organisms promotes the evolution of apose- coloration within Papilio. -
PDF Book of Climate Frequency Plots of Specific Bee Species Explanation Note: Frequency Plots of Identified Bee Species, Ordered by Family, for Each Climate Zone
JHR 79: 117–144 (2020) doi: 10.3897/jhr.79.57308 RESEARCH ARTICLE https://jhr.pensoft.net Morphometric comparisons and novel observations of diurnal and low-light-foraging bees James B. Dorey1, Erinn P. Fagan-Jeffries2, Mark I. Stevens3,4, Michael P. Schwarz1 1 College of Science and Engineering, Flinders University, GPO Box 2100, SA, 5001, Adelaide, Australia 2 Australian Centre for Evolutionary Biology & Biodiversity and School of Biological Sciences, The University of Adelaide, SA, 5000, Adelaide, Australia 3 Biological and Earth Sciences, South Australian Museum, GPO Box 234, SA, 5001, Adelaide, Australia 4 University of South Australia, Clinical and Health Sciences, SA 5000, Australia Corresponding author: James B. Dorey ([email protected]) Academic editor: M. Ohl | Received 6 August 2020 | Accepted 4 October 2020 | Published 30 October 2020 http://zoobank.org/D27A4B39-F0DD-474E-BA4B-A3C0140FECA6 Citation: Dorey JB, Fagan-Jeffries EP, Stevens MI, Schwarz MP (2020) Morphometric comparisons and novel observations of diurnal and low-light-foraging bees. Journal of Hymenoptera Research 79: 117–144. https://doi. org/10.3897/jhr.79.57308 Abstract Low-light adapted bees are substantially understudied components of the bee fauna, particularly in Aus- tralia. Whilst several species in Australia are thought to be adapted to low-light conditions, explicit records of these taxa actually foraging at twilight or night are absent from the scientific literature. We present the first observations of Australian bees foraging in low-light conditions as well as the first evidence of low-light foraging behaviour in the colletid bee subfamily, Hylaeinae. Using morphometrics of Austral- ian and more broadly-distributed diurnal, facultative low-light and obligate low-light adapted bees, we explore the use of morphological traits to objectively assess possible low-light behaviour and corroborate low-light collection events. -
Insect Pollinators and Their Conservation JEZS 2017; 5(3): 1121-1131 © 2017 JEZS Received: 07-03-2017 Accepted: 08-04-2017 Showket a Dar, GM Lone, Sajad H Parey, Gh
Journal of Entomology and Zoology Studies 2017; 5(3): 1121-1131 E-ISSN: 2320-7078 P-ISSN: 2349-6800 Insect pollinators and their conservation JEZS 2017; 5(3): 1121-1131 © 2017 JEZS Received: 07-03-2017 Accepted: 08-04-2017 Showket A Dar, GM Lone, Sajad H Parey, Gh. I Hassan and Bashir A Rather Showket A Dar Department of Entomology, RTCPPPM-SKUAST-K, Abstract Srinagar, Sher-e-Kashmir To address the concerns regarding insect pollinator populations in state of Jammu and Kashmir, we University of Agricultural surveyed and interviewed local farmers to gain a better understanding of current farming practices and Science and Technology, their effects on bee populations. We also consulted a number of apiary and agricultural experts during the Shalimar, Jammu and Kashmir, research phase from 2012 till 2016. The final product may be concluded in this manuscript which India describes various native and managed pollinator species and their habitat requirements. The paper further suggests best management practices that have the potential to help promote the growth and stability of GM Mir these pollinator populations in Kashmir division of J &K, India. Department of Entomology, RTCPPPM-SKUAST-K, Keywords: Kashmir, bees, pollination, conservation, colony Srinagar, Sheri-e-Kashmir University of Agricultural Science and Technology, Introduction Shalimar, Jammu and Kashmir, Kashmir agriculture and pollination problem India Jammu and Kashmir is a hill state having varied topography and the agriculture remains the backbone of economy of state with over 65 percent of its population depends on it. Agriculture GM Lone sector contribute around 27 percent to the State's income.