Flawke's Bay Twits $ At\; Is T *:';;Q*E Kit *: Hawkt:Bad \, Nth U Line Uniat! of Species, Habitats Grid Natural Lectures
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Shifting Ranges of Two Tree Weta Species (Hemideina Spp.)
Journal of Biogeography (J. Biogeogr.) (2014) 41, 524–535 ORIGINAL Shifting ranges of two tree weta species ARTICLE (Hemideina spp.): competitive exclusion and changing climate Mariana Bulgarella*, Steven A. Trewick, Niki A. Minards, Melissa J. Jacobson and Mary Morgan-Richards Ecology Group, IAE, Massey University, ABSTRACT Palmerston North, 4442, New Zealand Aim Species’ responses to climate change are likely to depend on their ability to overcome abiotic constraints as well as on the suite of species with which they interact. Responses to past climate change leave genetic signatures of range expansions and shifts, allowing inferences to be made about species’ distribu- tions in the past, which can improve our ability to predict the future. We tested a hypothesis of ongoing range shifting associated with climate change and involving interactions of two species inferred to exclude each other via competition. Location New Zealand. Methods The distributions of two tree weta species (Hemideina crassidens and H. thoracica) were mapped using locality records. We inferred the likely mod- ern distribution of each species in the absence of congeneric competitors with the software Maxent. Range interaction between the two species on an eleva- tional gradient was quantified by transect sampling. Patterns of genetic diver- sity were investigated using mitochondrial DNA, and hypotheses of range shifts were tested with population genetic metrics. Results The realized ranges of H. thoracica and H. crassidens were narrower than their potential ranges, probably due to competitive interactions. Upper and lower elevational limits on Mount Taranaki over 15 years revealed expan- sion up the mountain for H. thoracica and a matching contraction of the low elevation limits of the range of H. -
Weta Sometimes 5 Cicada Mouthparts? Earwig 3 Pairs Stick Insect 1 Pair with Fangs and Now Name One Poison Characteristic Each Wings? of the Other 6 Bugs Usually
Insects To be used with the Tangihua lions lodge program What is an insect All insects ? This insect have these has these Characteristics characteristics 6 legs What do you think? 8 legs More! Just circle the answer Wings Body parts? Or 2 No wings 3 A long thin body Legs? or 6 well developed legs 8 and long feelers More! I am a Eyes? Beetle 6 simple ones Fly 8 simple ones Moth Usually 2 but Giant Weta sometimes 5 Cicada Mouthparts? Earwig 3 pairs Stick insect 1 pair with fangs and Now name one poison characteristic each Wings? of the other 6 bugs Usually Draw a line showing who relates to what What habitats do you find insects in Weta To be used with the Tangihua lions lodge program Animals With out red blood or back bone Red blooded Invertebrates vertebrates Cephalopods Crustaceans Arthropod Plant animals Birds Fish Whales and Reptiles Land Cnidarians dolphins mammals Insects spider Wētā are arthropods and belong to the insect group because they have: 6 legs, 2 antennae, and a 3-part body Weta 5 types Tree Weta Ground Weta Giant Weta Tusked Weta Cave Weta Weta ? two compound eyes for close-up sight have these and three little eyes called ocelli to sense light and dark Antenna short tail-pieces called cerci to detect Femur vibrations Hind leg females have a long ovipositor at the- back to deposit eggs into the soil Front leg an ear on each front leg knee joint Ear palps alongside the jaws for tasting Ovipositor and smelling (like our tongue and nose) Spiracles spikey back legs that kick into the air Palps for defence and make a rasping sound as they come back down. -
Male Tree Weta Are Attracted to Cuticular Scent Cues but Do Not Discriminate According to Sex Or Among Two Closely Related Species
Received: 26 April 2017 | Revised: 7 June 2017 | Accepted: 3 July 2017 DOI: 10.1111/eth.12652 RESEARCH PAPER Male tree weta are attracted to cuticular scent cues but do not discriminate according to sex or among two closely related species Priscilla M. Wehi1,2 | Adrian Monks2 | Mary Morgan-Richards1 1Institute of Agriculture & Environment, Massey University, Palmerston North, Abstract New Zealand Recognition of conspecifics is an essential precursor of successful mating. Where 2 Landcare Research, Dunedin, New Zealand related species coexist, species discrimination might be important, but because related Correspondence species are similar, species signal recognition may actually be low. Chemical cues such Priscilla M. Wehi, Landcare Research, Private as cuticular hydrocarbons (CHCs) are frequently used by insects to identify suitable Bag 1930 Dunedin, 9054 New Zealand. Email: [email protected] sexual partners. We predicted that New Zealand tree weta (Hemideina spp.), a genus Funding information of nocturnal ensiferan Orthoptera that live both allopatrically and sympatrically, use This work was supported by New Zealand chemical signals from either frass or CHCs to find mates. In a series of six laboratory Foundation for Research, Science and Technology contract number UOWX0501, trials using both H. thoracica and H. crassidens, we found that male tree weta, but not and Postdoctoral fellowship MAUX0905; female tree weta, occupied cavities primed with female cuticular cues more often than Rutherford Discovery Fellowship 14- LCR- 001 to PMW; and Massey University MURF cavities without. However, males did not discriminate between chemical cues of male funding “What limits a weta?” to MMR. and female conspecifics, or between conspecifics and heterospecifics. -
Using Artificial Refuges to Translocate and Establish Auckland Tree Weta Hemideina Thoracica on Korapuki Island, New Zealand
Conservation Evidence (2005) 2, 94-95 www.ConservationEvidence.com Using artificial refuges to translocate and establish Auckland tree weta Hemideina thoracica on Korapuki Island, New Zealand Green C. Department of Conservation, PO Box 10420, The Terrace, Wellington 6143, New Zealand SUMMARY Two hundred wooden refuges were provided for the Auckland tree weta Hemideina thoracica . Within six months over half were used, 52 weta were transferred to Korapuki Island by plugging then translocating these refuges. After five years, there were over 500 individual tree wetas present on Korapuki. BACKGROUND habitat modification led to the loss of a variety of birds, lizards and large bodied invertebrates The Auckland tree weta Hemideina thoracica from Korapuki, including the Auckland tree (Orthoptera: Anostostomatidae) is a common weta. Restoration activities began with the species widely distributed over the upper half eradication of rats in 1987. Subsequently a of the North Island and its offshore islands, variety of native skink species were New Zealand. Their eggs hatch in spring and reintroduced through translocation from weta take 13 – 15 months to mature going neighbouring islands that had escaped invasion through eight to ten instars, with adults by the Pacific rat. In addition the island has reaching about 50 - 60 mm body length. been used to test new methods of invertebrate Although omnivorous, tree weta generally feed monitoring and translocation techniques, on fresh foliage in the canopy of forest trees particularly using artificial weta refuges and shrubs, with occasional fruit, flowers and designed to facilitate both these techniques. other invertebrates augmenting their diet. Thus the project aimed to re-establish the Typically tree weta hide during the day by Auckland tree weta on Korapuki Island using squeezing themselves into refuges such as a artificial refuges. -
Of New Zealand (Hemideina: Stenopelmatidae: Orthoptera)
New Zealand Entomologist, 1995, Val. 18 A new species of tree weta from the North Island of New Zealand (Hemideina: Stenopelmatidae: Orthoptera) MARYMORGAN-RICHARDS School of Biological Sciences, Victoria University of Wellington, PO Box 600, Wellington, New Zealand. ABSTRACT Hemideina trewicki, a new species of Stenopelmatidae from Hawkes Bay, is described. Morphologically it differs from H. crassidens only in the colouration of the pronotum but it can be distinguished using two allozyme loci (Ldh-2 and Pgm-I) and the number and gross morphology of the chromosomes. H. trewicki can be sympatric with H. thoracica and although a (probably sterile) F1 hybrid has been found, these two species have four fixed allozyme differences and karyotypes which clearly distinguish them. Keywords: tree weta, cryptic species, Hemideina crassidens, Hemideina thoracica, Hemideina treruicki, Orthoptera, Stenopelmatidae, New Zealand, karyotype, allozyme. INTRODUCTION Two species of tree weta are common and widespread in the North Island: Hemideina thoracica White, 1845 (Auckland tree weta) in the north to about 41 OS and H. crassidens (Rlanchard 1851) (Wellington tree weta) south of Mt Taranaki and Mt Ruapehu (Trewick & Morgan-Richards in press). Much confusion existed over their nomenclature until Ramsay & Bigelow (1978) clarified the situation. Since its original description, H. crassidens has been twice included in revisions where descriptions can be found under different names; Hutton (1897) referred to it as H. megacephala and Salmon (1950) as H. thoracica. Karny (1934), perhaps the last worker to examine the holotype, distinguished H. crassidem from H. thoracica by the presence of abdominal bands and a dark pronotum. In contrast the pronotum of H. -
Orthoptera: Ensifera)?
Zootaxa 4291 (1): 001–033 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2017 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4291.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:BD31B828-E7EF-46AD-B618-1BAAA2D63DBD Tackling an intractable problem: Can greater taxon sampling help resolve relationships within the Stenopelmatoidea (Orthoptera: Ensifera)? AMY G. VANDERGAST1,7, DAVID B. WEISSMAN2, DUSTIN A. WOOD3, DAVID C. F. RENTZ4, CORINNA S. BAZELET5 & NORIHIRO UESHIMA6 1U.S. Geological Survey, Western Ecological Research Center, San Diego Field Station, 4165 Spruance Road Suite 200, San Diego, CA 92101, USA. E-mail: [email protected] 2Department of Entomology, California Academy of Sciences, 55 Music Concourse Drive, San Francisco, CA 94118, USA. E-mail: [email protected] 3U.S. Geological Survey, Western Ecological Research Center, San Diego Field Station, 4165 Spruance Road Suite 200, San Diego, CA 92101, USA. E-mail: [email protected] 4School of Marine & Tropical Biology, James Cook University, Australia. E-mail: [email protected] 5Steinhardt Museum, Tel Aviv University, Department of Zoology, Sherman Building Rm. 403, Tel Aviv, Israel; Department of Conser- vation Ecology and Entomology, Stellenbosch University, Private Bag X1, Matieland 7602, South Africa. E-mail: [email protected] 61435-1 Kubocho, Matsusaka, Mie 515-0044, Japan. E-mail: [email protected] 7Corresponding Author Abstract The relationships among and within the families that comprise the orthopteran superfamily Stenopelmatoidea (suborder Ensifera) remain poorly understood. We developed a phylogenetic hypothesis based on Bayesian analysis of two nuclear ribosomal and one mitochondrial gene for 118 individuals (84 de novo and 34 from GenBank). -
Sex- and Season-Dependent Behaviour in a Flightless Insect, the Auckland Tree Weta (Hemideina Thoracica)
AvailableWehi et al.: on-line Seasonal at: http://www.newzealandecology.org/nzje/ behaviour patterns in weta 75 Sex- and season-dependent behaviour in a flightless insect, the Auckland tree weta (Hemideina thoracica) Priscilla M Wehi1,4*, Murray Jorgensen2 and Mary Morgan-Richards3 1Department of Biological Sciences, University of Waikato, Private Bag 3105, Hamilton 3240, New Zealand 2Department of Statistics, University of Waikato, Private Bag 3105, Hamilton 3240, New Zealand 3Institute of Natural Resources, Massey University, Private Bag 11222, Palmerston North, New Zealand 4Present address: CSAFE, University of Otago, P O Box 56, Dunedin, New Zealand *Author for correspondence (Email: [email protected]) Published online: 17 December 2012 Abstract: In a polygynous mating system, males frequently compete by locating and defending sites with resources essential to female survival and reproduction. We investigated seasonal changes in site occupancy in a sexually dimorphic, harem-forming insect, the Auckland tree weta (Hemideina thoracica). First we established artificial cavities as diurnal refuge cavities and potential harem guarding sites. We then examined cavity occupancy changes, and, based on our knowledge of prior occupants, determined sex-specific patterns of arrival, departure, and aggregation at a population level throughout the year. Both season and the sex of prior occupants influenced weta occupancy patterns. Most observations were of single females. However, both males and females moved into cavities previously occupied by a weta of the opposite sex more often than expected by chance alone. Females avoided cavities where other females were present, except during summer when most harems formed. In early summer, male and female tree weta previously living apart began co-habiting. -
Diet Selectivity in a Terrestrial Forest Invertebrate, the Auckland Tree Wētā, Across Three Habitat Zones
CORE Metadata, citation and similar papers at core.ac.uk Provided by Research Commons@Waikato Received: 11 September 2017 | Accepted: 4 December 2017 DOI: 10.1002/ece3.3763 ORIGINAL RESEARCH Diet selectivity in a terrestrial forest invertebrate, the Auckland tree wētā, across three habitat zones Matthew B. G. J. Brown1 | Chrissen E. C. Gemmill1 | Steven Miller2 | Priscilla M. Wehi3 1School of Science, University of Waikato, Hamilton, New Zealand Abstract 2Department of Mathematics and Insects are important but overlooked components of forest ecosystems in New Statistics, School of Computing and Zealand. For many insect species, information on foraging patterns and trophic rela- Mathematical Sciences, University of Waikato, Hamilton, New Zealand tionships is lacking. We examined diet composition and selectivity in a large- bodied 3Centre for Sustainability, University of Otago insect, the Auckland tree wētā Hemideina thoracica, in three habitat zones in a lowland and Manaaki Whenua Landcare Research, New Zealand forest. We asked whether H. thoracica selectively forage from available Dunedin, New Zealand plant food sources, and whether these choices were lipid- rich compared to nonpre- Correspondence ferred available plants. We also identified the proportion of invertebrates in their frass Priscilla M. Wehi, Manaaki Whenua Landcare Research, Dunedin, New Zealand. as a proxy for omnivory. From reconnaissance plot sampling, together with fecal frag- Email: [email protected] ment analysis, we report that more than 93% of individual tree wētā had eaten inver- Funding information tebrates before capture. Additionally, wētā in the highest elevation hillslope habitat University of Waikato; Royal Society of New zone consumed significantly fewer species of plants on average than wētā on the low- Zealand, Grant/Award Number: 14-LCR-001 elevation terrace habitat. -
The Effects of Rodents on Ground Dwelling Arthropods in the Waitakere Ranges
The Effects of Rodents on Ground Dwelling Arthropods in the Waitakere Ranges A thesis submitted to the Auckland University of Technology in fulfilment of the Degree Master of Philosophy Peter A. King January 2007 TABLE OF CONTENTS ATTESTATION …………………………….…………….…….………………….…....8 ACKNOWLEDGEMENTS………………………………………………………….……9 ABSTRACT ……………………...……………………….……….………….……....…11 1 INTRODUCTION.............................................................................................................. 13 1.1 GONDWANALAND ORIGINS OF NEW ZEALAND’S ARTHROPODS.............. 14 1.2 IMPACTS OF HUMAN COLONISATION............................................................... 17 1.3 ARTHROPODS IN THE DIETS OF INTRODUCED PREDATORS....................... 19 1.4 IMPACT OF INTRODUCED PREDATORS ON NATIVE VERTEBRATES ......... 22 1.5 EFFECTS OF PREDATORS ON NATIVE ARTHROPODS.................................... 24 1.5.1 Research on Offshore Islands .......................................................................24 1.5.2 Research on the Mainland ............................................................................29 1.6 IMPACT OF HABITAT STRUCTURE ON ARTHROPOD POPULATIONS......... 32 1.7 ARTHROPODS AS INDICATORS OF ENVIRONMENTAL CHANGE................ 33 1.8 SUMMARY ................................................................................................................ 35 1.9 AIMS OF THIS RESEARCH ..................................................................................... 36 2 METHODS .........................................................................................................................38 -
What Weta Want: Colour Preferences of a Frugivorous Insect
Arthropod-Plant Interactions (2010) 4:267–276 DOI 10.1007/s11829-010-9109-0 ORIGINAL PAPER What weta want: colour preferences of a frugivorous insect Nik Fadzly • K. C. Burns Received: 24 March 2010 / Accepted: 18 October 2010 / Published online: 31 October 2010 Ó Springer Science+Business Media B.V. 2010 Abstract Plants use colours as signals to attract mutual- consistent preferences for colours other than red indicate ists and repel antagonists. Fleshy-fruits are often conspic- that weta might be responsible for the unusual colours of uously coloured to signal different types of information fleshy-fruits in New Zealand. including fruit maturity and spatial location. Previous work on fruit colour selection focus on large diurnal vertebrates, Keywords Colour Á Fleshy-fruits Á New Zealand Á yet fruit colours are perceived differently by frugivores Weta with different types of visual systems. Here, we tested whether a nocturnal, frugivorous, seed-dispersing insect selects fruits based on their pigmentation and whether Introduction different lighting conditions affect fruit colour selection. We captured 20 Wellington tree weta (Hemideina crassi- Most plants are sessile and often rely on animals for the dens) from a forest reserve on the North Island of New movement of seeds and pollen. In order to attract animal Zealand and brought them into laboratory conditions to test mutualists, plants often use colour signals. Fruits and their fruit colour preferences. The fruits of Coprosma flowers are often brightly coloured to attract frugivores and acerosa, a native shrub species that naturally produces pollinators (see van der Pijl 1972; Janson 1983; Willson translucent, blue-streaked fruits, were dyed either red or et al. -
RESEARCH ARTICLE Mechanical Filtering for Narrow-Band Hearing in the Weta
778 The Journal of Experimental Biology 214, 778-785 © 2011. Published by The Company of Biologists Ltd doi:10.1242/jeb.050187 RESEARCH ARTICLE Mechanical filtering for narrow-band hearing in the weta Kathryn Lomas1, Fernando Montealegre-Z2,*, Stuart Parsons1, Larry H. Field3 and Daniel Robert2 1University of Auckland, School of Biological Sciences, Private Bag 92019, Auckland 1142, New Zealand, 2School of Biological Sciences, University of Bristol, Woodland Road, Bristol BS8 1UG, UK and 3School of Biological Sciences, University of Canterbury, Edward Percival Field Station, The Esplanade, Kaikoura 7300, New Zealand *Author for correspondence ([email protected]) Accepted 22 November 2010 SUMMARY This paper constitutes a major attempt to associate tympanic deflections with the mechanoreceptor organ location in an acoustic insect. The New Zealand tree weta (Hemideina thoracica) has tympanal ears located on each of the prothoracic tibiae. The tympana exhibit a sclerotized oval plate, membranous processes bulging out from the tibial cuticle and many loosely suspended ripples. We used microscanning laser Doppler vibrometry to determine how such a tympanal membrane vibrates in response to sound and whether the sclerotized region plays a role in hearing. The tympanum displays a single resonance at the calling frequency of the male, an unusual example of an insect tympana acting as a narrow bandpass filter. Both tympana resonate in phase with the stimulus and with each other. Histological sections show that the tympanal area is divided into two distinct regions, as in other ensiferans. An oval plate lies in the middle of a thickened region and is surrounded by a transparent and uniformly thin region. -
Assessment of Natural Heritage for the Review of the Central Hawke's Bay
Assessment of Natural Heritage for the Review of the Central Hawke’s Bay District Plan NATURAL HERITAGE REVIEW OF THE CENTRAL HAWKE’S BAY DISTRICT I Table of Contents Executive Summary ................................................................................................................ 1 1 Introduction .................................................................................................................... 5 1.1 Context and Purpose 5 1.2 Objectives 5 1.3 Approach to the Assessment 6 1.4 Location 7 2 Policy Framework ......................................................................................................... 8 2.1 RMA Summary 8 2.2 Determining Ecological Significance 9 2.3 Existing Plan Provisions 10 2.4 HBRC Provisions 10 2.5 Examples of Other Approaches 11 2.6 Tools for Policy Development 11 3 Methodology ................................................................................................................ 13 3.1 Literature Review 13 3.2 GIS Mapping and Analysis 13 3.2.1 Base spatial data 13 3.2.2 Design scale 14 3.2.3 Minimum Mapping Unit (MMU) 14 3.2.4 Descriptive attributes 14 3.2.5 Significance assessments 14 4 Ecological Character of the CHBD ............................................................................. 14 4.1 General Overview 14 4.2 Heretaunga ED 16 4.3 Ruahine ED 16 4.4 Eastern Hawke’s Bay ED 17 4.5 Puketoi ED 18 5 Threatened Biodiversity of the CHBD ........................................................................ 19 5.1 Extent of Nationally Threatened Environments