Nzbotsoc No 82 Dec 2005
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TRILEPIDEA Newsletter of the New Zealand Plant Conservation Network NO. 185 CONFERENCE REGISTRATION OPEN NOW! May 2019 We invite you to register for the 2019 Australasian Systematic Botany Society and New Deadline for next issue: Zealand Plant Conservation Network joint conference to be held at the Museum of New Monday 20 May 2019 Zealand Te Papa Tongarewa, Wellington, New Zealand in the last week of November. SUBMIT AN ARTICLE Start planning now! Spaces in workshops and fi eld trips are limited, so register early to TO THE NEWSLETTER get your top choices. Contributions are welcome Check out the recently updated conference website to get all the important details to the newsletter at any time. The closing date for about conference dates, venue, accommodation, programme, keynote speakers, fi eld articles for each issue is trips, workshops, silent auction, and more! approximately the 15th of each month. The conference theme, ‘Taxonomy for Plant Conservation – Ruia mai i Rangiātea’ aims to capitalise on the vast expertise of our two societies. There will be multiple upskilling Articles may be edited and used in the newsletter and/ workshops, three days of symposia, and a chance to explore Wellington’s forests and or on the website news page. rugged coastlines on our fi ve diff erent full-day fi eld trips. The Network will publish Feel free to contact the organising committee by email if you have any queries: almost any article about [email protected], otherwise go to the conference website (https://systematics. plants and plant conservation with a particular focus on the ourplants.org/) to keep up to date with developments, or follow us on Facebook or plant life of New Zealand and Twitter for announcements. -
NZ Orchid Key: a New Smartphone App for Identifying Native Orchids Murray Dawson1, Jeremy Rolfe, Michael Pratt and Ian St George
NZ Orchid Key: a new smartphone app for identifying native orchids Murray Dawson1, Jeremy Rolfe, Michael Pratt and Ian St George Smartphones have rapidly become the device of choice for New Zealanders and the rest of the world. Their processing power, storage capacity, and portability have come of age, making it possible to run comprehensive productivity apps including identification tools. Uptake of this technology will continue to increase into the foreseeable future. It is timely then that a powerful app for identifying native orchids is now available for smartphones and tablets from the Android Google Play Store and Apple’s iTunes (Fig. 1A–E)2. E Fig. 1 Screenshots of the NZ Orchid Key C app. A, icon, illustrating the mauve sun orchid (Thelymitra malvina). B, start-up screen. C, feature (character) list. D, entity (species) list. E, part of a built-in species profile. This free app, called the NZ Orchid Key, is easy-to-use, has lots of A colourful photographs, and covers a wide array of plant characters3, including leaves, flowers, habitats, and distribution for identifying native orchids. Users choose whichever characters in the app match the orchid specimen they are identifying through a process of elimination. If a user needs help to understand what a particular character state means, they can bring up an explanation page for it. Each species within the app is supported by a descriptive profile, providing all the information needed to verify the identification. Species D profiles include links out to online B resources on native orchids – the 1 Landcare Research, PO Box 69040, Lincoln 7640, Canterbury, New Zealand; [email protected] 2 https://play.google.com/store/apps/details?id=com.lucidcentral.mobile.nz_orchid and https://itunes.apple.com/us/app/nz-orchid-key/ id1063192594?mt=8 3 In total, 43 characters and 212 character states were chosen for identifying native orchids in the key. -
Ersidad Michoacana De San Nicolás De Hidalgo
UNIVERSIDAD MICHOACANA DE SAN NICOLÁS DE HIDALGO PROGRAMA INSTITUCIONAL DE MAESTRÍA EN CIENCIAS BIOLÓGICAS ÁREA TEMÁTICA: ECOLOGÍA Y CONSERVACIÓN SISTEMA DE APAREAMIENTO, CARACTERIZACIÓN ECOLÓGICA Y PROPAGACIÓN IN VITRO DE Cuitlauzina pendula La Llave & Lex (ORCHIDACEAE) TESIS QUE PARA OBTENER EL GRADO ACADÉMICO DE MAESTRA EN CIENCIAS PRESENTA VERÓNICA ADRIANA PÉREZ DECELIS DIRECTORA DE TESIS: DC. IRENE ÁVILA DÍAZ CO.-DIRECTOR: DC. RAFAEL SALGADO GARCIGLIA MORELIA, MICHOACÁN, MÉXICO AGOSTO DE 2013 Cuitlauzina pendula La Llave & Lex. Fotografía: Pérez-Decelis V. A. 2013 “Dejar de creer en el logró de tus sueños es no hacerlos realidad, pues antes de ser realidad han sido eso, sueños”. Esforzarte por lograrlos no es sólo desearlo, es hacerlo todo lo posible y a veces lo imposible por hacerlos una realidad. DEDICATORIA A Dios por darme la fortaleza para seguir adelante y enseñarme en cada uno de mis errores y tropiezos una forma de aprendizaje. Por permitirme ser madre, esposa, hija, hermana y haberme rodeado de amigas (os) llenos de luz que estuvieron siempre a mi lado. Por conservar mi esencia a pesar de lo dura que fue la vida conmigo y por permitirme realizar mis sueños. A mis padres: Domingo (†) por seguir siendo un ejemplo en mi vida e inculcarme la fe en Dios, el deseo de superación, perseverancia, coraje y amor en todo lo que hago. Por haberme permitido conocerlo, amarlo y aún en su ya larga ausencia estar presente en mis logros. Carmelita: Mujer incansable que me enseño a luchar, trabajar, aferrarme a la vida y a levantarme cuando caí. Gracias por ser mi fuerza y pilar en cada momento, por apoyarme con Nikté y darle tu amor incondicional, cariño y sobre todo por creer y apoyarme en la realización de mis sueños y aspiraciones. -
Orchids of the Wellington District
Orchids of the Wellington District A. P. DRUCE The hills around Wellington have at the present time one of the richest orchid floras in New Zealand. Only the Auckland district surpasses Wellington. Yet few people are aware of this and fewer still have searched closely for these fascinating plants. It is not surprising therefore that several of the orchids growing about Wellington have remained unrecorded for a long time. Altogether forty-two orchid species and varieties are now known from this district. For the purpose of this article the Wellington district is taken to include all the Rimutakas, all the western hills and to extend up to the tops of the Tararua Mountains. Very few orchids are found on the western hills (i.e., the hills to the west of the Hutt Valley and Wellington Harbour) from Cook Strait north to about Haywards. Mixed bush clothed these hills originally—beech was absent. The soils differ from those across the harbour and second-growth is more often tauhinu than manuka. In some way or other the conditions are not right for most of the orchids. Over the rest of the district however, wherever manuka holds sway there are large numbers of orchids of many species. On Mrs. Prasophyllum colensoi (left), Adenochilus gracilis (centre) and Microtis unifolia (right). 4 h Pterostylis nana (left) and Pterostylis barbata (right). Samson's section at Pinehaven for instance over twenty species may be found and a sample area nearby showed that at least 10,000 indi- vidual orchids grow per acre in that locality. There cannot have been anything like these numbers a century ago for most of the manuka land was in bush and the orchids of the bush, besides being different, are comparatively few in number. -
Nzbotsoc No 64 June 2001
NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 64 JUNE 2001 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 Subscriptions The 2001 ordinary and institutional subs are $18 (reduced to $15 if paid by the due date on the subscription invoice). The 2001 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 28th February 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 September 2001 issue (Number 65) is 25 August 2001. Please post contributions to: Joy Talbot 23 Salmond Street Christchurch 8002 Send contributions by e-mail to [email protected]. Files can be in WordPerfect (version 8 or earlier), MS Word (version 6 or earlier) or saved as RTF or ASCII. -
Ecology of Vascular Epiphytes in Urban Forests with Special Reference to the Shrub Epiphyte Griselinia Lucida
Ecology of vascular epiphytes in urban forests with special reference to the shrub epiphyte Griselinia lucida A thesis submitted in partial fulfilment of the requirements for the degree of Master of Science in Biological Sciences at The University of Waikato by Catherine Louise Bryan 2011 Abstract This research investigated the ecology of vascular epiphytes and vines in the Waikato region of the North Island, and the water relations of the shrub hemiepiphyte Griselinia lucida. The main goal was to develop robust recommendations for the inclusion of epiphytic species in urban forest restoration projects. To achieve this, three broad questions were addressed: 1. How are vascular epiphytes and vines distributed throughout the nonurban and urban areas of the Waikato region, and how does this compare to other North Island areas? 2. Why are some epiphyte and vine species absent from urban Hamilton and what opportunities exist for their inclusion in restoration projects? 3. How does Griselinia lucida respond to desiccation stress and how does this compare to its congener G. littoralis? To investigate questions one and two, an ecological survey of the epiphyte communities on host trees in Waikato (n=649) and Taranaki (n=101) was conducted, alongside canopy microclimate monitoring in five Waikato sites. Results show that epiphyte and vine populations in Hamilton City forests represent only 55.2 % of the total Waikato species pool, and have a very low average of 0.8 epiphyte species per host. In contrast, the urban forests of Taranaki support 87.9 % of the local species pool and have an average of 5.5 species per host tree. -
Earina Aestivalis
Earina aestivalis COMMON NAME Bamboo orchid, summer earina SYNONYMS None FAMILY Orchidaceae AUTHORITY Earina aestivalis Cheeseman FLORA CATEGORY Vascular – Native ENDEMIC TAXON Yes ENDEMIC GENUS Earina aestivalis in flower. Photographer: Bec No Stanley ENDEMIC FAMILY No STRUCTURAL CLASS Orchids NVS CODE EARAES CHROMOSOME NUMBER 2n = 40, 41 CURRENT CONSERVATION STATUS 2012 | Not Threatened PREVIOUS CONSERVATION STATUSES 2009 | Not Threatened 2004 | Not Threatened DISTRIBUTION Endemic. North, South, Stewart and Chatham Islands. HABITAT Earina aestivalis in flower. Photographer: Bec Coastal forest, where it is usually a low epiphyte on tree trunks and Stanley branches. Occasionally found on cliff faces and rock outcrops FEATURES Epiphytic or rupestral, rhizomatous, perennial, producing numerous leafy, unbranched, long persistent, wiry, cane- like stems up to 600 mm long. Rhizomes extensive, much intertwined and firmly attached to substrate, fleshy, more or less spongy, initially creamy white maturing buff-yellow. Leaf-sheaths imbricating, persistent, distichously arranged, 5-12 mm long, 4-8 mm diameter, not split, tubular, flattened, each overlapping with and covering the lower third to one half of the leaf-sheath above, exposed surface ivory to pale whitish-yellow, distinctly dark maculate with broad, long oblong to oblong-ovoid dark purple-black spots. Leaf-sheath junction with leaf lamina distinctly flared. Leaves weakly flexuose scarcely curved in upper portion; lamina short-lived, disarticulating at leaf- sheath junction, prominent 3-nerved, 60-100 x 6-8 mm, green to dark green, lanceolate, tapering in upper third gradually to an acute, minutely acicular tip; lateral veins conspicuous, midrib of upper lamina deeply and prominently channelled. Inflorescence a racemose panicle. -
Generic Delimitation and Macroevolutionary Studies in Danthonioideae (Poaceae), with Emphasis on the Wallaby Grasses, Rytidosperma Steud
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2010 Generic delimitation and macroevolutionary studies in Danthonioideae (Poaceae), with emphasis on the wallaby grasses, Rytidosperma Steud. s.l. Humphreys, Aelys M Abstract: Ein Hauptziel von evolutionsbiologischer und ökologischer Forschung ist die biologische Vielfalt zu verstehen. Die systematische Biologie ist immer in der vordersten Reihe dieser Forschung gewesen and spielt eine wichtiger Rolle in der Dokumentation und Klassifikation von beobachteten Diversitätsmustern und in der Analyse von derer Herkunft. In den letzten Jahren ist die molekulare Phylogenetik ein wichtiger Teil dieser Studien geworden. Dies brachte nicht nur neue Methoden für phylogenetische Rekonstruktio- nen, die ein besseres Verständnis über Verwandtschaften und Klassifikationen brachten, sondern gaben auch einen neuen Rahmen für vergleichende Studien der Makroevolution vor. Diese Doktorarbeit liegt im Zentrum solcher Studien und ist ein Beitrag an unser wachsendes Verständnis der Vielfalt in der Natur und insbesondere von Gräsern (Poaceae). Gräser sind schwierig zu klassifizieren. Dies liegt ein- erseits an ihrer reduzierten Morphologie – die an Windbestäubung angepasst ist – und anderseits an Prozessen wie Hybridisation, die häufig in Gräsern vorkommen, und die die Bestimmung von evolution- shistorischen Mustern erschweren. Gräser kommen mit über 11,000 Arten auf allen Kontinenten (ausser der Antarktis) vor und umfassen einige der -
Recent Vegetation Succession and Flora of Macauley Island, Southern Kermadec Islands
www.aucklandmuseum.com Recent vegetation succession and flora of Macauley Island, southern Kermadec Islands Peter J. de Lange Department of Conservation Abstract A revised listing of the flora of Macauley Island is presented and aspects of its composition discussed. A vascular flora of 92 taxa (including two hybrid combinations and two unnamed entities) and 50 bryophytes is recorded here for the island. Six seaweeds are also recorded from the intertidal zone of the north-eastern coastline of Macauley. Twenty-two taxa (10 Vascular plants, seven liverworts and five mosses) are considered new records for the Kermadec Islands, and 59 taxa (22 vascular plants, 10 liverworts and 27 mosses) are additions to the known flora of Macauley Island. The flora of the island has increased considerably since goats were exterminated from the island in 1970. The vegetation of the island is documented, using broad, empirically derived vegetation associations. Eleven associations are recognised and described and the vegetation succession of the island discussed. While the dominant vegetation cover on the island is still a dense monospecific Hypolepis fernland, a treeland of Homalanthus polyandrus is now developing. It is suggested that this has happened because kiore (Rattus exulans) may have been successfully eradicated from the island in 2006. Notes are made on the condition of the islands vegetation associations in the wake of Tropical Cyclone Bune, which struck the island on 28 March 2011. It is also suggested that the vegetation succession of Macauley Island needs no direct human intervention to make conditions more suitable for sea bird nesting. Keywords Kermadec Islands; Macauley Island flora; vascular plants; bryophytes; cyclone-damage; vegetation associations; vegetation succession; Homalanthus; rat predation INTRODUCTION formed the scoriaceous deposits and lava flows around Mt Haszard; or, by deep erosion gullies and ravines. -
Cf. Eria Dacrydium. Syn. E. Biflora. Dactyl-: Used in Combwds., Ref. Daktylos: Digit
dacrydium: ref. dakrydion: a little tear (: tear-drop). cf. Eria dacrydium. syn. E. biflora. dactyl-: used in combwds., ref. daktylos: digit. Mostly taken as: finger, but can also be: toe. For any organ or part alluded to resemble a finger; having, or like a finger. dactyla: digit; finger. cf. Lepanthes dactyla. x Dactyleucorchis: Soó 1966. Noted the name was taken from Dactylorhiza and Leucorchis, as it seemed to have qualities of both. syn. x Pseudorhiza P.F.Hunt. dactylifera: finger + bearing. cf. Eulophia dactylifera. dactyliferum: finger + see -fer: bearing. Alluding to the labellum callus. cf. Oncidium dactyliferum. dactylina: digit; finger + like. cf. Lepanthes dactylina. dactylinum: digit; finger + like. cf. Cryptocentrum peruvianum ssp.dactylinum. Dactylis: see dactyl-: digit; finger, or toe. eg. Dactylis glomerata. x Dactylitella: P.F.Hunt & Summerh.1965. Noted the name was taken from the parents, reported to be a cross of Nigritella x Dactylorhiza. syn. x Dactylodenia. x Dactylocamptis: P.F.Hunt & Summerh.1965. Noted the name is taken from the parents, the result of Anacamptis x Dactylorhiza. ex Switzerland, cf. x Dactylocamptis weberi (M.Schulze) Soó 1966. Noted as monotypic. dactyloceras: finger + horn. cf. Podangis dactyloceras. Dactyloceras: Garay & H.R.Sweet 1968: finger + horn. syn. x Orchidactylorhiza. dactyloclinium: finger + small bed. cf. Epidendrum dactyloclinium. x Dactylodenia: Garay & H.R.Sweet 1966. Noted the name is taken from the parents as it’s a cross of Dactylorhiza x Gymnadenia. eg. x Dactylodenia varia. Listed as ex westn. Europe and Great Britain. dactylodes: digit; finger + resembling. cf. Dendrobium dactylodes. Dactyloglossum: P.F.Hunt & Summerh.1965. Noted the name is taken from the parents as it was thought to be a cross of Coeloglossum x Dactylorhiza. -
Pittosporum Kirkii: Autecology of an Endemic Shrub Epiphyte
http://researchcommons.waikato.ac.nz/ Research Commons at the University of Waikato Copyright Statement: The digital copy of this thesis is protected by the Copyright Act 1994 (New Zealand). The thesis may be consulted by you, provided you comply with the provisions of the Act and the following conditions of use: Any use you make of these documents or images must be for research or private study purposes only, and you may not make them available to any other person. Authors control the copyright of their thesis. You will recognise the author’s right to be identified as the author of the thesis, and due acknowledgement will be made to the author where appropriate. You will obtain the author’s permission before publishing any material from the thesis. Pittosporum kirkii: autecology of an endemic shrub epiphyte A thesis submitted in partial fulfilment of the requirements for the degree of Master of Science in Biological Sciences at The University of Waikato by Kirsty Jane Myron 2012 i “The most striking and beautiful of the New Zealand [Pittosporum] species” - Kirk (1899) Bird‟s eye view of a female epiphytic Pittosporum kirkii at the top of a rimu snag. Photo taken by A. Hawcroft (Department of Conservation 2009) during an aerial foliar browse survey of the Matemateaonga Range, inland Taranaki. ii Abstract This research investigated the autecology of the New Zealand endemic shrub epiphyte Pittosporum kirkii (Pittosporaceae). Pittosporum kirkii most frequently displays an epiphytic lifestyle, perched amongst nest epiphytes in the canopies of emergent or canopy trees in old-growth forest. The main objective of this research was to enhance the understanding of Pittosporum kirkii, with a focus on ecological, morphological and physiological characteristics. -
Systematics of California Grasses (Poaceae)
TWO Systematics of California Grasses (Poaceae) PAUL M. PETERSON AND ROBERT J. SORENG The grass family (Poaceae or Gramineae) is the fourth largest relationships among organisms) of the major tribes of flowering plant family in the world and contains about California grasses. 11,000 species in 800 genera worldwide. Twenty-three gen- era contain 100 or more species or about half of all grass Morphology species, and almost half of the 800 genera are monotypic or diatypic, i.e., with only one or two species (Watson and The most important feature of grasses (Poaceae) is a one- Dallwitz 1992, 1999). seeded indéhiscent fruit (seed coat is fused with the ovary Over the last 150 years the grass flora of California has wall), known as a caryopsis or grain (see Figure 2.1; Peterson been the subject of considerable attention by botanists. 2003). The grain endosperm is rich in starch, although it can Bolander (1866) prepared the first comprehensive list, recog- contain protein and significant quantities of lipids. The nizing 112 grasses from California, of which 31 were intro- embryo is located on the basal portion of the caryopsis and ductions. Thurber (1880) mentions 175 grasses in California, contains high levels of protein, fats, and vitamins. The stems and Beetle (1947) enumerates 400 known species. It is inter- are referred to as culms, and the roots are fibrous and princi- esting to note that Crampton (1974) recognized 478 grasses pally adventitious or arising from lower portions of the in California, and of these, 175 were introduced and 156 were culms. Silica-bodies are a conspicuous component of the reported as annuals (we report 152 annuals here).