Operational Forest Restoration Plan for Kukutaaruhe Gully
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Toward a Resolution of Campanulid Phylogeny, with Special Reference to the Placement of Dipsacales
TAXON 57 (1) • February 2008: 53–65 Winkworth & al. • Campanulid phylogeny MOLECULAR PHYLOGENETICS Toward a resolution of Campanulid phylogeny, with special reference to the placement of Dipsacales Richard C. Winkworth1,2, Johannes Lundberg3 & Michael J. Donoghue4 1 Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, Caixa Postal 11461–CEP 05422-970, São Paulo, SP, Brazil. [email protected] (author for correspondence) 2 Current address: School of Biology, Chemistry, and Environmental Sciences, University of the South Pacific, Private Bag, Laucala Campus, Suva, Fiji 3 Department of Phanerogamic Botany, The Swedish Museum of Natural History, Box 50007, 104 05 Stockholm, Sweden 4 Department of Ecology & Evolutionary Biology and Peabody Museum of Natural History, Yale University, P.O. Box 208106, New Haven, Connecticut 06520-8106, U.S.A. Broad-scale phylogenetic analyses of the angiosperms and of the Asteridae have failed to confidently resolve relationships among the major lineages of the campanulid Asteridae (i.e., the euasterid II of APG II, 2003). To address this problem we assembled presently available sequences for a core set of 50 taxa, representing the diver- sity of the four largest lineages (Apiales, Aquifoliales, Asterales, Dipsacales) as well as the smaller “unplaced” groups (e.g., Bruniaceae, Paracryphiaceae, Columelliaceae). We constructed four data matrices for phylogenetic analysis: a chloroplast coding matrix (atpB, matK, ndhF, rbcL), a chloroplast non-coding matrix (rps16 intron, trnT-F region, trnV-atpE IGS), a combined chloroplast dataset (all seven chloroplast regions), and a combined genome matrix (seven chloroplast regions plus 18S and 26S rDNA). Bayesian analyses of these datasets using mixed substitution models produced often well-resolved and supported trees. -
Apoidea (Insecta: Hymenoptera). Fauna of New Zealand 57, 295 Pp. Donovan, B. J. 2007
Donovan, B. J. 2007: Apoidea (Insecta: Hymenoptera). Fauna of New Zealand 57, 295 pp. EDITORIAL BOARD REPRESENTATIVES OF L ANDCARE R ESEARCH Dr D. Choquenot Landcare Research Private Bag 92170, Auckland, New Zealand Dr R. J. B. Hoare Landcare Research Private Bag 92170, Auckland, New Zealand REPRESENTATIVE OF UNIVERSITIES Dr R.M. Emberson c/- Bio-Protection and Ecology Division P.O. Box 84, Lincoln University, New Zealand REPRESENTATIVE OF M USEUMS Mr R.L. Palma Natural Environment Department Museum of New Zealand Te Papa Tongarewa P.O. Box 467, Wellington, New Zealand REPRESENTATIVE OF OVERSEAS I NSTITUTIONS Dr M. J. Fletcher Director of the Collections NSW Agricultural Scientific Collections Unit Forest Road, Orange NSW 2800, Australia * * * SERIES EDITOR Dr T. K. Crosby Landcare Research Private Bag 92170, Auckland, New Zealand Fauna of New Zealand Ko te Aitanga Pepeke o Aotearoa Number / Nama 57 Apoidea (Insecta: Hymenoptera) B. J. Donovan Donovan Scientific Insect Research, Canterbury Agriculture and Science Centre, Lincoln, New Zealand [email protected] Manaaki W h e n u a P R E S S Lincoln, Canterbury, New Zealand 2007 4 Donovan (2007): Apoidea (Insecta: Hymenoptera) Copyright © Landcare Research New Zealand Ltd 2007 No part of this work covered by copyright may be reproduced or copied in any form or by any means (graphic, electronic, or mechanical, including photocopying, recording, taping information retrieval systems, or otherwise) without the written permission of the publisher. Cataloguing in publication Donovan, B. J. (Barry James), 1941– Apoidea (Insecta: Hymenoptera) / B. J. Donovan – Lincoln, N.Z. : Manaaki Whenua Press, Landcare Research, 2007. (Fauna of New Zealand, ISSN 0111–5383 ; no. -
The Species of Alseuosmia (Alseuosmiaceae)
New Zealand Journal of Botany, 1978, Vol. 16: 271-7. 271 The species of Alseuosmia (Alseuosmiaceae) RHYS O. GARDNER Department of Botany, University of Auckland, Private Bag, Auckland, New Zealand (Received 15 September 1977) ABSTRACT A new species Alseuosmia turneri R. 0. Gardner (Alseuosmiaceae Airy Shaw) from the Volcanic Plateau, North Island, New Zealand is described and illustrated. A. linariifolia A. Cunn. is reduced to a variety of A. banksii A. Cunn. and A. quercifolia A. Cunn. is given hybrid status (=^4. banksii A. Cunn. x A. macrophylla A. Cunn.). A key to the four Alseuosmia species, synonymy, and a generalised distribution map are given. A. pusilla Col. is illustrated for the first time. INTRODUCTION judged to be frequent between only one pair of Allan Cunningham (1839) described eight species and the "excessive variability" lies mostly species of a new flowering plant genus Alseuosmia there. from material collected in the Bay of Islands region by Banks and Solander in 1769, by himself in 1826 and 1838, and by his brother Richard in 1833-4. The A NEW SPECIES OF ALSEUOSMIA species, all shrubs of the lowland forest, were sup- A. CUNN. posed to differ from one another chiefly in the shape and toothing of their leaves. An undescribed species of Alseuosmia from the Hooker (1852-5, 1864), with the benefit of Waimarino region of the Volcanic Plateau has been additional Colenso and Sinclair material, reduced known for some time (Cockayne 1928, p. 179; A. P. Cunningham's species to four, but stated that these Druce in Atkinson 1971). The following description four species were "excessively variable". -
Otanewainuku ED (Report Prepared on 13 August 2013)
1 NZFRI collection wish list for Otanewainuku ED (Report prepared on 13 August 2013) Fern Ally Isolepis cernua Lycopodiaceae Isolepis inundata Lycopodium fastigiatum Isolepis marginata Lycopodium scariosum Isolepis pottsii Psilotaceae Isolepis prolifera Tmesipteris lanceolata Lepidosperma australe Lepidosperma laterale Gymnosperm Schoenoplectus pungens Cupressaceae Schoenoplectus tabernaemontani Chamaecyparis lawsoniana Schoenus apogon Cupressus macrocarpa Schoenus tendo Pinaceae Uncinia filiformis Pinus contorta Uncinia gracilenta Pinus patula Uncinia rupestris Pinus pinaster Uncinia scabra Pinus ponderosa Hemerocallidaceae Pinus radiata Dianella nigra Pinus strobus Phormium cookianum subsp. hookeri Podocarpaceae Phormium tenax Podocarpus totara var. totara Iridaceae Prumnopitys taxifolia Crocosmia xcrocosmiiflora Libertia grandiflora Monocotyledon Libertia ixioides Agapanthaceae Watsonia bulbillifera Agapanthus praecox Juncaceae Alliaceae Juncus articulatus Allium triquetrum Juncus australis Araceae Juncus conglomeratus Alocasia brisbanensis Juncus distegus Arum italicum Juncus edgariae Lemna minor Juncus effusus var. effusus Zantedeschia aethiopica Juncus sarophorus Arecaceae Juncus tenuis var. tenuis Rhopalostylis sapida Luzula congesta Asparagaceae Luzula multiflora Asparagus aethiopicus Luzula picta var. limosa Asparagus asparagoides Orchidaceae Cordyline australis x banksii Acianthus sinclairii Cordyline banksii x pumilio Aporostylis bifolia Asteliaceae Corunastylis nuda Collospermum microspermum Diplodium alobulum Commelinaceae -
Are Cabbage Trees Worth Anything? Relating Ecological and Human Values in the Cabbage Tree, Fl Kouka
Are cabbage trees worth anything? Relating ecological and human values in the cabbage tree, fl kouka PHILIP SIMPSON piles, and fence posts. The cabbage tree exemplifies the relationship be Cabbage trees entered 'New Zealand' along tropical tween people and plants, not only the whole.tree itself archipelagos some 15 million years ago.' They have but also its parts, the leaves, the internal tissues, and adapted to the vicissitudes of sea-level, mountain build their biochemistry. ing and erosion, and climate change, and have evolved When Polynesian settlers named the New Zealand into different species and regional forms. A remarkable cabbage trees 'ti' they were retaining a tradition of set of structural and physiological features has devel using its tropical relative, Cordyline fruticosa (formerly oped to equip them for survival in a changeable and known as C. terminalis). They brought it with them and sometimes extreme environment. called it tl pore, 'the 'short' cabbage tree. European It was the qualities of strength and durability that whalers and sealers adopted 'cabbage palm' from Cook's were seized on by Maori, and they favoured some or first voyage because the tips of palms were often eaten selected new forms to satisfy their daily needs. The as a vegetable ('cabbage') by sailors, and because of the same qualities of survival underscore Pakeha respect archetypal similarity between cabbage trees and tropi for cabbage trees. They too have recognised variety and cal palms that the temperate travellers had seen for the have bred new forms to satisfy their aesthetic mores. A first time. It is perhaps the leafy, tropical look com sense of national identity has grown around the cab bined with temperate strength that account for the world bage tree and people have been shocked by the epi fame of cabbage trees. -
Plant Charts for Native to the West Booklet
26 Pohutukawa • Oi exposed coastal ecosystem KEY ♥ Nurse plant ■ Main component ✤ rare ✖ toxic to toddlers coastal sites For restoration, in this habitat: ••• plant liberally •• plant generally • plant sparingly Recommended planting sites Back Boggy Escarp- Sharp Steep Valley Broad Gentle Alluvial Dunes Area ment Ridge Slope Bottom Ridge Slope Flat/Tce Medium trees Beilschmiedia tarairi taraire ✤ ■ •• Corynocarpus laevigatus karaka ✖■ •••• Kunzea ericoides kanuka ♥■ •• ••• ••• ••• ••• ••• ••• Metrosideros excelsa pohutukawa ♥■ ••••• • •• •• Small trees, large shrubs Coprosma lucida shining karamu ♥ ■ •• ••• ••• •• •• Coprosma macrocarpa coastal karamu ♥ ■ •• •• •• •••• Coprosma robusta karamu ♥ ■ •••••• Cordyline australis ti kouka, cabbage tree ♥ ■ • •• •• • •• •••• Dodonaea viscosa akeake ■ •••• Entelea arborescens whau ♥ ■ ••••• Geniostoma rupestre hangehange ♥■ •• • •• •• •• •• •• Leptospermum scoparium manuka ♥■ •• •• • ••• ••• ••• ••• ••• ••• Leucopogon fasciculatus mingimingi • •• ••• ••• • •• •• • Macropiper excelsum kawakawa ♥■ •••• •••• ••• Melicope ternata wharangi ■ •••••• Melicytus ramiflorus mahoe • ••• •• • •• ••• Myoporum laetum ngaio ✖ ■ •••••• Olearia furfuracea akepiro • ••• ••• •• •• Pittosporum crassifolium karo ■ •• •••• ••• Pittosporum ellipticum •• •• Pseudopanax lessonii houpara ■ ecosystem one •••••• Rhopalostylis sapida nikau ■ • •• • •• Sophora fulvida west coast kowhai ✖■ •• •• Shrubs and flax-like plants Coprosma crassifolia stiff-stemmed coprosma ♥■ •• ••••• Coprosma repens taupata ♥ ■ •• •••• •• -
1999 New Zealand Botanical Society
NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 57 SEPTEMBER 1999 New Zealand Botanical Society President: Jessica Beever Secretary/Treasurer: Anthony Wright Committee: Bruce Clarkson, Colin Webb, Carol West Address: c/- Canterbury Museum Rolleston Avenue CHRISTCHURCH 8001 NEW ZEALAND Subscriptions The I999 ordinary and institutional subs are $18 (reduced to $15 if paid by the due date on the subscription invoice). The 1999 student sub, available to full-time students, is $9 (reduced to $7 if paid by the due date on the subscription invoice). Back issues of the Newsletter are available at $2.50 each from Number 1 (August 1985) to Number 46 (December 1996), $3.00 each from Number 47 (March 1997) to Number 50 (December 1997), and $3.75 each from Number 51 (March 1998) onwards. Since 1986 the Newsletter has appeared quarterly in March, June, September and December. New subscriptions are always welcome and these, together with back issue orders, should be sent to the Secretary/Treasurer (address above). Subscriptions are due by 28 February of each year for that calendar year. Existing subscribers are sent an invoice with the December Newsletter for the next year's subscription which offers a reduction if this is paid by the due date. If you are in arrears with your subscription a reminder notice comes attached to each issue of the Newsletter. Deadline for next issue The deadline for the December 1999 issue (Number 58) is 26 November 1999. Please forward contributions to: Dr Carol J. West, c/- Department of Conservation PO Box 743 Invercargill Contributions may be provided on an IBM compatible floppy disc (Word) or by e-mail to [email protected] Cover Illustration Plagiochila ramosissima with antheridial branches. -
Assessing Pollination and Fruit Dispersal in Fuchsia Excorticata (Onagraceae)
RobertsonNew Zealand et al.—Pollination Journal of Botany, and 2008, dispersal Vol. in46 Fuchsia: 299–314 299 0028–825X/08/4603–0299 © The Royal Society of New Zealand 2008 Assessing pollination and fruit dispersal in Fuchsia excorticata (Onagraceae) ALastaIR W. ROBErtsON cases very frequently by silvereyes, which also oc- Ecology, Institute of Natural Resources casionally rob nectar from flowers. We confirmed Massey University that hermaphrodites account for more than half the Private Bag 11222 plants in all populations, are fully self-compatible, Palmerston North 4474, New Zealand and can autonomously self in the absence of pollina- [email protected] tors (especially in plants with smaller herkogamy). Fruit production in hermaphrodites and (particularly) JENNY J. LADLEY females was frequently pollen-limited (mean Pollen DAVE KELLY Limitation Indices of 0.17 and 0.40, respectively), School of Biological Sciences and was correlated with visual assessments of pol- University of Canterbury len loads on the stigma, a useful index of pollinator Private Bag 4800 service. A comparison of the proportion of ripe or Christchurch 8140, New Zealand overripe fruit on branches exposed to birds versus KatE L. MCNUTT branches enclosed in wire cages showed that un- Ecology, Institute of Natural Resources caged fruit on Kapiti Island is removed almost as Massey University soon as it is ripe but on the mainland it persists for Private Bag 11222 much longer. The proportion of ripe or overripe Palmerston North 4474, New Zealand compared to green fruit is therefore an approximate index of dispersal service. Both indices may be use- PAUL G. PETERSON ful to managers concerned with measuring the level Landcare Research of mutualism service provided by native birds. -
Polarised Light Microscopy: an Old Technique Casts New Light on Māori Textile Plants
Polarised light microscopy: an old technique casts new light on Māori textile plants Rachel A. Paterson1, Bronwyn J. Lowe1*, Catherine A. Smith1, Janice M. Lord2, Roka Ngarimu-Cameron3 1Department of Applied Sciences/Te Tari Pūtaiao Whakahāngai, University of Otago/Te Whare Wānanga o Otāgo, PO Box 56, Dunedin/Ōtepoti 9054, New Zealand/Aotearoa 2Department of Botany/Te Tari Huaota o Otāgo, University of Otago/Te Whare Wānanga o Otāgo, PO Box 56, Dunedin/Ōtepoti 9054, New Zealand/Aotearoa 32806 State Highway 35, Hawai Bay, Opotiki 3197, New Zealand/Aotearoa Corresponding author: *[email protected] ABSTRACT Understanding the composition of an artefact has ramifications for advancing human history and behaviour knowledge, providing cultural information about trade, agricultural practices and adaptation to new environments. However, accurate plant identification from artefacts is problematic, since textile production, age, dirt and/or conservation treatments obscure morphological features, and specimen size and/or ethical considerations hamper modern analytical methods. This study tested the efficacy of polarised light microscopy (PLM) in the identification of New Zealand plant species commonly used in Māori textiles, and demonstrates that morphological and birefringent features observed using PLM have the potential to distinguish between- and within- plant genera. KEYWORDS Māori textiles, New Zealand flax, Phormium, Cordyline, Freycinetia, sign of elongation, modified Herzog test, plant material identification INTRODUCTION Accurate plant material identification is critical for advancing study of material culture, since an object’s composition provides an insight into its origin, additionally revealing important cultural information such as human interactions and emigration pathways (Schaffer 1981; Jakes et al. 1994). However, one of the main challenges for accurate identification of plant species in textile artefacts is the scarcity of distinct morphological features, evident from whole plants or individual leaves (e.g. -
Breeding Systems and Reproduction of Indigenous Shrubs in Fragmented
Copyright is owned by the Author of the thesis. Permission is given for a copy to be downloaded by an individual for the purpose of research and private study only. The thesis may not be reproduced elsewhere without the permission of the Author. Breeding systems and reproduction of indigenous shrubs in fragmented ecosystems A thesis submitted in partial fulfilment of the requirements for the degree of Doctor of Philosophy III Plant Ecology at Massey University by Merilyn F Merrett .. � ... : -- �. � Massey University Palrnerston North, New Zealand 2006 Abstract Sixteen native shrub species with various breeding systems and pollination syndromes were investigated in geographically separated populations to determine breeding systems, reproductive success, population structure, and habitat characteristics. Of the sixteen species, seven are hermaphroditic, seven dioecious, and two gynodioecious. Two of the dioecious species are cryptically dioecious, producing what appear to be perfect, hermaphroditic flowers,but that functionas either male or female. One of the study species, Raukauaanomalus, was thought to be dioecious, but proved to be hermaphroditic. Teucridium parvifolium, was thought to be hermaphroditic, but some populations are gynodioecious. There was variation in self-compatibility among the fo ur AIseuosmia species; two are self-compatible and two are self-incompatible. Self incompatibility was consistent amongst individuals only in A. quercifolia at both study sites, whereas individuals in A. macrophylia ranged from highly self-incompatible to self-compatible amongst fo ur study sites. The remainder of the hermaphroditic study species are self-compatible. Five of the species appear to have dual pollination syndromes, e.g., bird-moth, wind-insect, wind-animal. High levels of pollen limitation were identified in three species at fo ur of the 34 study sites. -
NZ BOT SOC Sept2014
NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 117 September 2014 New Zealand Botanical Society President: Anthony Wright Secretary/Treasurer: Ewen Cameron Committee: Bruce Clarkson, Colin Webb, Carol West Address: c/- Canterbury Museum Rolleston Avenue CHRISTCHURCH 8013 Webmaster: Murray Dawson URL: www.nzbotanicalsociety.org.nz Subscriptions The 2014 ordinary and institutional subscriptions are $25 (reduced to $18 if paid by the due date on the subscription invoice). The 2014 student subscription, available to full-time students, is $12 (reduced to $9 if paid by the due date on the subscription invoice). Back issues of the Newsletter are available at $7.00 each. Since 1986 the Newsletter has appeared quarterly in March, June, September and December. New subscriptions are always welcome and these, together with back issue orders, should be sent to the Secretary/Treasurer (address above). Subscriptions are due by 28 February each year for that calendar year. Existing subscribers are sent an invoice with the December Newsletter for the next years subscription which offers a reduction if this is paid by the due date. If you are in arrears with your subscription a reminder notice comes attached to each issue of the Newsletter. Deadline for next issue The deadline for the December 2014 issue is 25 November 2014. Please post contributions to: Lara Shepherd Museum of New Zealand Te Papa Tongarewa 169 Tory St Wellington 6021 Send email contributions to [email protected]. Files are preferably in MS Word, as an open text document (Open Office document with suffix “.odt”) or saved as RTF or ASCII. Macintosh files can also be accepted. -
Phylogeny and Phylogenetic Nomenclature of the Campanulidae Based on an Expanded Sample of Genes and Taxa
Systematic Botany (2010), 35(2): pp. 425–441 © Copyright 2010 by the American Society of Plant Taxonomists Phylogeny and Phylogenetic Nomenclature of the Campanulidae based on an Expanded Sample of Genes and Taxa David C. Tank 1,2,3 and Michael J. Donoghue 1 1 Peabody Museum of Natural History & Department of Ecology & Evolutionary Biology, Yale University, P. O. Box 208106, New Haven, Connecticut 06520 U. S. A. 2 Department of Forest Resources & Stillinger Herbarium, College of Natural Resources, University of Idaho, P. O. Box 441133, Moscow, Idaho 83844-1133 U. S. A. 3 Author for correspondence ( [email protected] ) Communicating Editor: Javier Francisco-Ortega Abstract— Previous attempts to resolve relationships among the primary lineages of Campanulidae (e.g. Apiales, Asterales, Dipsacales) have mostly been unconvincing, and the placement of a number of smaller groups (e.g. Bruniaceae, Columelliaceae, Escalloniaceae) remains uncertain. Here we build on a recent analysis of an incomplete data set that was assembled from the literature for a set of 50 campanulid taxa. To this data set we first added newly generated DNA sequence data for the same set of genes and taxa. Second, we sequenced three additional cpDNA coding regions (ca. 8,000 bp) for the same set of 50 campanulid taxa. Finally, we assembled the most comprehensive sample of cam- panulid diversity to date, including ca. 17,000 bp of cpDNA for 122 campanulid taxa and five outgroups. Simply filling in missing data in the 50-taxon data set (rendering it 94% complete) resulted in a topology that was similar to earlier studies, but with little additional resolution or confidence.