EXPRESSIONS WHIRINAKI EDUCATIONAL RESOURCE Expressions Whirinaki Arts & Entertainment Centre Is Upper Hutt’S Own Art Hub
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
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. -
How Non-Nestmates Affect the Cohesion of Swarming Groups in Social Spiders
Insect. Soc. 55 (2008) 355 – 359 0020-1812/08/040355-5 Insectes Sociaux DOI 10.1007/s00040-008-1011-8 Birkhäuser Verlag, Basel, 2008 Research article How non-nestmates affect the cohesion of swarming groups in social spiders A.-C. Mailleux1, R. Furey2, F. Saffre1, B. Krafft4 and J.-L. Deneubourg1 1 Service dÉcologie Sociale, Campus de la Plaine, CP 231, UniversitØ Libre de Bruxelles, 1050 Brussels, Belgium, e-mail: [email protected], [email protected], [email protected] 2 Harrisburg University of Science and Technology 866, HBG.UNIV 215, Market Street, Harrisburg, Pennsylvania 17101 USA, e-mail: [email protected] 3 UniversitØ Nancy 2, Rue Baron Louis, BP 454 Code postal 54001 Ville Nancy Cedex, France, e-mail: [email protected] Received 30 October 2007; revised 3 April and 19 May 2008; accepted 22 May 2008. Published Online First 17 June 2008 Abstract. In social biology, it is often considered that an Fletcher and Michener, 1987). Unlike most vertebrate organized society cannot exist without exclusion behav- and invertebrate societies (Hepper, 1986; Fletcher and iour towards newcomers from another nest. Unlike most Michener, 1987), social spiders accept artificially intro- vertebrate and invertebrate social species, social spiders duced immigrants without apparent discrimination or such as Anelosimus eximius accept unrelated migrants agonistic behaviour (Evans, 1999). This absence of group without agonistic behaviour. Does it imply that spiders closure prompts some authors to suggest that spiders cannot recognize non-nestmates from nestmates or is cannot identify newcomers (Buskirk, 1981; Howard, there any evidence of recognition without aggression ? In 1982; Darchen and Delage-Darchen, 1986; Pasquet et order to answer this question, we studied behavioural al., 1997). -
Flawke's Bay Twits $ At\; Is T *:';;Q*E Kit *: Hawkt:Bad \, Nth U Line Uniat! of Species, Habitats Grid Natural Lectures
, , ,,,..*. *'.~,*, . , ** **~ I*~ tv, *..',.- 4'1 I, ' it**.*, , , *. * 44 ,,! ~**~ $1. \ -* * .,,;. f, *- , **, 3* .* ,J re* *. ^ ,~ I * ,* ,, ^ "*'. 441 , ,*.A, * ~*\,*t* J The open braids of the Totaekuri River Flawke's Bay twits $ at\; is t *:';;q*e Kit *: hawkt:bad \, nth u line uniat! of species, habitats Grid natural lectures. Hawke's Bay is a special part of New Zealand with a It, :ae from one threat can be exacerbated by the effects of variety of species, habitats and natural features, other threats acting together, i. e. habitat fragmentation Before humans settled here, almost the entire lowlands combined with invasive species. and hill country of the region would have been covered Despite extensive modification, Hawke's Bay contains a in dense forests, rich in birdlife. Clearance of vegetation great diversity of landscapes, habitats, plants, animals, cover started with early Maori and continued with and areas of high natural and historic value. There the arrival of Fakeba leaving a legacy of almost total are areas in Flawke's Bay which support a diverse and modification of the natural ecosystems. significant range of indigenous species and ecosystems including the Kaweka Ranges, Lake Walkaremoana, Forest dearance, wedand drainage, engineering of Pekapel<a Wetland, Whal{a}d Lagoon, AhuririEstuary, waterways and redamation of coastal margins has Blowhard Bush, Cape Kidnappers Sanctuary and been necessary for the development of our cities and Boundary Stream. Many of these sites are in very good the region. We are able to live safely and prosper in a condition. Several endemic species which at. e nationally beautiful part of the world but development has had a considerable impact on indigenous biodiversity. -
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. -
Chilopoda; Scolopendridae
Bijdragen tot dl Dierkunde, 55 (1): 125-130 — 1985 Possible species isolation mechanisms in some scolopendrid centipedes (Chilopoda; Scolopendridae) by J.G.E. Lewis Taunton School, Taunton, Somerset TA2 6AD, England the femur of Abstract are seen on Eupolybothrus spp. Various other lithobiid secondary sexual sexual characters in dis- Secondary centipedes are briefly characters have been reviewed by Lewis (1981). cussed and it is that the the suggested spines on prefemora of the described Differences type above are of the last pair of legs in some scolopendrids are used in presumably associated with mating behaviour specific discrimination prior to mating. The hypothesis is in which male and female head discussed with reference of the come together to Scolopendra spp. eastern Mediterranean,north-east Africa and Arabia. to tail, and the antennae and the last pair of legs Where species of Scolopendra with identical The virtually are tapped. morphological adaptations in spinulation on the last legs are sympatric, a large size dif- the males would serve for the femalesto identify ference exists between them. different and sex. It is that in where the species suggested some genera prefemoral have been inhibited. In spines are absent, speciation may the where be absent genus Otostigmus spines may or spine similar in number of other patterns are very a species DIMORPHISM IN SCOLOPENDRIDAE secondary sexual characters have developed. Sexual is also in dimorphism seen the scolopen- INTRODUCTION dromorph family Scolopendridae. In Scolopendra morsitans Linnaeus the dorsal side of the Centipedes not infrequently exhibit secondary prefemur, femur and sometimes the tibiaof the last of is sexual characters. -
Crocodylus Moreletii
ANFIBIOS Y REPTILES: DIVERSIDAD E HISTORIA NATURAL VOLUMEN 03 NÚMERO 02 NOVIEMBRE 2020 ISSN: 2594-2158 Es un publicación de la CONSEJO DIRECTIVO 2019-2021 COMITÉ EDITORIAL Presidente Editor-en-Jefe Dr. Hibraim Adán Pérez Mendoza Dra. Leticia M. Ochoa Ochoa Universidad Nacional Autónoma de México Senior Editors Vicepresidente Dr. Marcio Martins (Artigos em português) Dr. Óscar A. Flores Villela Dr. Sean M. Rovito (English papers) Universidad Nacional Autónoma de México Editores asociados Secretario Dr. Uri Omar García Vázquez Dra. Ana Bertha Gatica Colima Dr. Armando H. Escobedo-Galván Universidad Autónoma de Ciudad Juárez Dr. Oscar A. Flores Villela Dra. Irene Goyenechea Mayer Goyenechea Tesorero Dr. Rafael Lara Rezéndiz Dra. Anny Peralta García Dr. Norberto Martínez Méndez Conservación de Fauna del Noroeste Dra. Nancy R. Mejía Domínguez Dr. Jorge E. Morales Mavil Vocal Norte Dr. Hibraim A. Pérez Mendoza Dr. Juan Miguel Borja Jiménez Dr. Jacobo Reyes Velasco Universidad Juárez del Estado de Durango Dr. César A. Ríos Muñoz Dr. Marco A. Suárez Atilano Vocal Centro Dra. Ireri Suazo Ortuño M. en C. Ricardo Figueroa Huitrón Dr. Julián Velasco Vinasco Universidad Nacional Autónoma de México M. en C. Marco Antonio López Luna Dr. Adrián García Rodríguez Vocal Sur M. en C. Marco Antonio López Luna Universidad Juárez Autónoma de Tabasco English style corrector PhD candidate Brett Butler Diseño editorial Lic. Andrea Vargas Fernández M. en A. Rafael de Villa Magallón http://herpetologia.fciencias.unam.mx/index.php/revista NOTAS CIENTÍFICAS SKIN TEXTURE CHANGE IN DIASPORUS HYLAEFORMIS (ANURA: ELEUTHERODACTYLIDAE) ..................... 95 CONTENIDO Juan G. Abarca-Alvarado NOTES OF DIET IN HIGHLAND SNAKES RHADINAEA EDITORIAL CALLIGASTER AND RHADINELLA GODMANI (SQUAMATA:DIPSADIDAE) FROM COSTA RICA ..... -
Spiders 27 November-5 December 2018 Submitted: August 2019 Robert Raven
Bush Blitz – Namadgi, ACT 27 Nov-5 Dec 2018 Namadgi, ACT Bush Blitz Spiders 27 November-5 December 2018 Submitted: August 2019 Robert Raven Nomenclature and taxonomy used in this report is consistent with: The Australian Faunal Directory (AFD) http://www.environment.gov.au/biodiversity/abrs/online-resources/fauna/afd/home Page 1 of 12 Bush Blitz – Namadgi, ACT 27 Nov-5 Dec 2018 Contents Contents .................................................................................................................................. 2 List of contributors ................................................................................................................... 2 Abstract ................................................................................................................................... 4 1. Introduction ...................................................................................................................... 4 2. Methods .......................................................................................................................... 4 2.1 Site selection ............................................................................................................. 4 2.2 Survey techniques ..................................................................................................... 4 2.2.1 Methods used at standard survey sites ................................................................... 5 2.3 Identifying the collections ......................................................................................... -
SA Spider Checklist
REVIEW ZOOS' PRINT JOURNAL 22(2): 2551-2597 CHECKLIST OF SPIDERS (ARACHNIDA: ARANEAE) OF SOUTH ASIA INCLUDING THE 2006 UPDATE OF INDIAN SPIDER CHECKLIST Manju Siliwal 1 and Sanjay Molur 2,3 1,2 Wildlife Information & Liaison Development (WILD) Society, 3 Zoo Outreach Organisation (ZOO) 29-1, Bharathi Colony, Peelamedu, Coimbatore, Tamil Nadu 641004, India Email: 1 [email protected]; 3 [email protected] ABSTRACT Thesaurus, (Vol. 1) in 1734 (Smith, 2001). Most of the spiders After one year since publication of the Indian Checklist, this is described during the British period from South Asia were by an attempt to provide a comprehensive checklist of spiders of foreigners based on the specimens deposited in different South Asia with eight countries - Afghanistan, Bangladesh, Bhutan, India, Maldives, Nepal, Pakistan and Sri Lanka. The European Museums. Indian checklist is also updated for 2006. The South Asian While the Indian checklist (Siliwal et al., 2005) is more spider list is also compiled following The World Spider Catalog accurate, the South Asian spider checklist is not critically by Platnick and other peer-reviewed publications since the last scrutinized due to lack of complete literature, but it gives an update. In total, 2299 species of spiders in 67 families have overview of species found in various South Asian countries, been reported from South Asia. There are 39 species included in this regions checklist that are not listed in the World Catalog gives the endemism of species and forms a basis for careful of Spiders. Taxonomic verification is recommended for 51 species. and participatory work by arachnologists in the region. -
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. -
A New Scolopendromorph Centipede from Belize
SOIL ORGANISMS Volume 81 (3) 2009 pp. 519–530 ISSN: 1864 - 6417 Ectonocryptoides sandrops – a new scolopendromorph centipede from Belize Arkady A. Schileyko Zoological Museum of Moscow State Lomonosov University, Bolshaja Nikitskaja Str.6, 103009, Moscow, Russia; e-mail: [email protected] Abs tract A new representative of the rare subfamily Ectonocryptopinae (Scolopocryptopidae) is described from western Belize as Ectonocryptoides sandrops sp. nov. Both previously known representatives of this subfamily ( Ectonocryptops kraepelini Crabill, 1977 and Ectonocryptiodes quadrimeropus Shelley & Mercurio, 2005) and the new species have been compared and the taxonomic status of the latter has been analysed. Keywords: Ectonocryptopinae, new species, Belize 1. Introduction Some years ago, working on exotic Scolopendromorpha from a collection of Prof. Alessandro Minelli I found one very small (ca 11–12 mm long) scolopendromorph centipede (Fig. 1). It had been collected by Francesco Barbieri in Mountain Pine Ridge of Western Belize (Fig. 2). With 23 pedal segments this blind centipede clearly belongs to the family Scolopocryptopidae Pocock, 1896. According to the very special structure of the terminal legs I have identified this animal as a new species of the very rare subfamily Ectonocryptopinae Shelley & Mercurio, 2005. The structure of the terminal legs (= legs of the ultimate body segment) is of considerable taxonomic importance in the order Scolopendromorpha. Commonly the terminal leg consists of 5 podomeres (prefemur, femur, tibia, tarsus 1, tarsus 2) and pretarsus. The first four podomeres are always present, when tarsus 2 and the pretarsus may both be absent. The terminal podomeres are the most transformable ones. There are six principle (or basic) types of terminal legs among scolopendromorph centipedes: 1) ‘common’ shape (the most similar to the locomotory legs), which is the least specialised (Fig. -
Royal Society of Western Australia, 97: 57–64, 2014
WA Science—Journal of the Royal Society of Western Australia, 97: 57–64, 2014 Arachnida (Arthropoda: Chelicerata) of Western Australia: overview and prospects M S HARVEY * Department of Terrestrial Zoology, Western Australian Museum, Locked Bag 49, Welshpool DC, WA 6986, Australia. [email protected]. The history of the study of arachnids (spiders, scorpions, ticks, mites and their relatives) in Western Australia is briefly reviewed, and the main periods of activity are documented: 1860s–1910s, between the wars, after World War II, and the modern era. The fauna consists of at least 1400 named species (but the mite fauna is imperfectly documented), and it is estimated that ~6000 species exist, the majority of which are currently undescribed KEYWORDS: history, pseudoscorpions, scorpions, spiders, taxonomy. INTRODUCTION nowadays known as Missulena granulosum (Cambridge). This species is quite common throughout southwestern The arachnid fauna of Western Australia represents a Australia where it persists in woodland habitats. The fascinating tableau of ancient relictual species and more next arachnid to be described was Idiops blackwalli recently arrived invaders. While the spiders (order Cambridge (1870) based on an adult male collected from Araneae) and mites (superorder Acari) are numerically Swan River. The species was quickly transferred to a new dominant, representatives of six other orders— genus by Ausserer (1871). Idiommata blackwalli is a large, Scorpiones, Pseudoscorpiones, Opiliones, Schizomida, impressive species still common in the Perth region. The Amblypygi and Palpigradi (Figure 1)—have been found trapdoor spiders Aganippe latior (based on a female from in the state. The size of the fauna is unknown, but ‘West Australia’), Eriodon insignis (based on a male from certainly comprises several thousand species, the Swan River), and E. -
He Kete Hauora Taia Final
HE KETE HAUORA TAIAO A BICULTURAL ECOLOGICAL ASSESSMENT FRAMEWORK By SARA MELISSA BELCHER A thesis submitted to the Victoria University of Wellington in fulfilment of the requirements for the degree of Doctor of Philosophy Victoria University of Wellington 2020 Tuhinga whakarāpopoto: Abstract Ka mau tonu ngā taonga tapu o ngā matua tupuna Koinei ngā taonga i tuku iho, na te ātua Hold fast to the treasures of the ancestors For they are the treasures that have been handed down to us by God’ (Dymond, 2013, p. 274) Ecologists, resource managers, landowners and iwi generally strive to manage biodiversity on their whenua as obliged by legislation. This may include restoration, protection, the mitigation of negative human impacts, or the prevention of further habitat loss. Mainstream ecological science and resource management (ERM) usually guides management decisions and provides evidence of management effectiveness. However, ecological science can struggle with stochastic and complex biological systems. Māori have hundreds of years of environmental knowledge and understanding that could be utilised by mainstream resource managers to enhance society's combined knowledge. An assessment tool that places mātauranga at its core can introduce a Māori perspective, privilege Māori knowledge, enable holistic co-management, re/introduce social values and create a common ground on which the two paradigms can connect. He Kete Hauora Taiao is an environmental assessment framework for terrestrial habitats constructed on Māori ecological health indicators by applying them to quantitative ecological scientific data. He Kete Hauora Taiao is built on the Driver – Pressure – State/Condition – Indicator – Response framework (K. F. D. Hughey, Cullen, Kerr, & Cook, 2004).