New Zealand Mistletoe
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Arachnid Ecology in New Zealand, Exploring
1 Arachnid ecology in New Zealand, exploring 2 unknown and poorly understood factors. 3 James Crofts-Bennett. 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 “A thesis submitted in fulfilment of the degree of Master of Science [1] in Botany [2] at the 21 University of Otago, Dunedin, New Zealand” 22 2020 23 1 24 Index 25 26 Abstract………………………………………………………………………………………5. 27 Chapter 1. Introduction……………………………………………………………………...7. 28 1.1 The importance of spiders………………………………………………………...7. 29 1.2 The influence of habitat structural complexity on spider distribution and 30 abundance…………………………………………………………………………......8. 31 1.3 Invasive rodents in the context of New Zealand Araneae………………………...9. 32 1.4 Thesis structure and aims………………………………………………………..14. 33 Chapter 2. The effect of habitat structural complexity on spider abundance and diversity..15. 34 2.1 Introduction ……………………………………………………………………..15. 35 Figure 2.1: Seasonal deciduous vegetation cover…………………………...16. 36 Figure 2.2: Seasonal deciduous vegetation cover with mistletoe parasites…16. 37 2.2 Methods…………………………………………………………………………17. 38 Figure 2.3: Examples of foliage samples……………………………………18. 39 Table 2.1: Sampling locations, dates and host data…………………………19. 40 2.2.1 Statistical Analyses……………………………………………………………20. 41 2.3 Results…………………………………………………………………………...20. 42 Figure 2.4: Total invertebrates sampled in summer, plotted………………..22. 43 Figure 2.5: Total invertebrates sampled in winter, plotted………………….23. 44 Table 2.2: Paired t-tests of host plant invertebrate populations……………..25. 45 2.4 Discussion……………………………………………………………………….26. 46 Chapter 3. A novel non-kill Araneae trap: test with regards to vegetation type versus 47 location 48 effects………………………………………………………………………………………..28. 49 3.1 Introduction……………………………………………………………………...28. -
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. -
Peraxilla Colensoi
Peraxilla colensoi COMMON NAME Scarlet mistletoe, korukoru, pirita, roeroe SYNONYMS Elytranthe colensoi (Hook.f.) Engl. Loranthus colensoi Hook. f. FAMILY Loranthaceae AUTHORITY Peraxilla colensoi (Hook.f.) Tiegh. FLORA CATEGORY Vascular – Native ENDEMIC TAXON Yes ENDEMIC GENUS Yes Peraxilla colensoi, Catlins. Photographer: John Barkla ENDEMIC FAMILY No STRUCTURAL CLASS Trees & Shrubs - Dicotyledons NVS CODE PERCOL CHROMOSOME NUMBER 2n= 24 CURRENT CONSERVATION STATUS 2012 | At Risk – Declining | Qualifiers: CD PREVIOUS CONSERVATION STATUSES 2009 | At Risk – Declining | Qualifiers: CD 2004 | Gradual Decline BRIEF DESCRIPTION Fleshy shrub to 3m wide growing on outer branches of beech trees with glossy green fleshy paired leaves and masses of red tubular flowers. Leaves to 8cm long, smooth with a red edge. Flowers to 2.5cm long. Fallen petals litter forest floor under plants. Fruit yellow. Photographer: Brian Molloy DISTRIBUTION North and South Island, but common only in southern parts of the South Island. HABITAT A parasite mainly found in silver beech forest but has been recorded on 16 host species (9 exotic) in New Zealand including red beech and black beech. Tui (Prosthemadera novaeseelandiae) and bellbird (Anthonis melanura) disperse this species in the North Island. FEATURES A shrub up to 3 m across. It parasitises further out on branches of its host than Peraxilla tetrapetala. The veins on leaves are hardly evident and only the midrib is conspicuous. Leaf tips are never notched and the leaves themselves are large and never blistered. The leaves sit in pairs on opposite sides of the stem and are thick and have a leathery texture. Leaf margins are usually smooth with red slightly rough margins. -
Explosive New Zealand Mistletoe Example, 4 of 7 Flowers on Sheet AK103910)
SCIENTIFIC CORRESPONDENCE pattern, as do herbarium sheets (for Explosive New Zealand mistletoe example, 4 of 7 flowers on sheet AK103910). Trilepidea almost certainly SIR- Many flowers of the mistletoe arium sheets show an even more special had more complex explosive flowers than Peraxilla tetrapetala (Loranthaceae) in New ized explosive mechanism than in Peraxilla. Peraxilla. Such specialization may have Zealand open from the bottom (f in the We discovered explosive flower opening rendered Trilepidea more sensitive to figure) rather than the top (d); Kuijtl called in both endemic New Zealand Peraxilla reduced bird densities due to introduced this an "unsolved mystery ... we cannot species when we noted that flower buds mammalian predators, contributing to its even guess at the meaning of this bizarre bagged for hand pollination almost never rapid and puzzling5 decline. performance." Here we report that flower opened (3/394 for P. tetrapetala, 1/82 for P. Explosive flower opening is well known buds of P. tetrapetala and P. colensoi open colensoi). The petals remained fused at the in other mistletoes6, including many of from the top only when twisted by top, while eventually undergoing abscis the 230 species in Africa3, and a few a bird, a form of 'explosive' flower open sion from their base (fin the figure). Field species in India7, Java, New Guinea and ing common in Africa but previously observations of unbagged flowers revealed South America1•6. However, this is the unknown in Australasia. Kuijt's "bizarre that they were opened by two native first report from Australasia. The New performance" is simply the consequence of honeyeaters (Meliphagidae ): tuis (Pros Zealand flora generally displays few flowers not being visited by birds. -
Spatial Variation in Impacts of Brushtail Possums on Two Loranthaceous Mistletoe Species
SWEETAPPLE:Available on-line at:POSSUM http://www.newzealandecology.org/nzje/ IMPACTS ON MISTLETOE 177 Spatial variation in impacts of brushtail possums on two Loranthaceous mistletoe species Peter J. Sweetapple Landcare Research, PO Box 40, Lincoln 7640, New Zealand (Email: [email protected]) Published on-line: 8 October 2008 ___________________________________________________________________________________________________________________________________ Abstract: Browsing by introduced brushtail possums is linked to major declines in mistletoe abundance in New Zealand, yet in some areas mistletoes persist, apparently unaffected by the presence of possums. To determine the cause of this spatial variation in impact I investigated the abundance and condition (crown dieback and extent of possum browse cover) of two mistletoes (Alepis flavida, Peraxilla tetrapetala) and abundance and diet of possums in two mountain beech (Nothofagus solandri var. cliffortioides) forests in the central-eastern South Island of New Zealand. Mistletoe is common and there are long-established uncontrolled possum populations in both forests. Mistletoes were abundant (216–1359 per hectare) and important in possum diet (41–59% of total diet), but possum density was low (c. 2 per hectare) in both areas. Possum impacts were slight with low browse frequencies and intensities over much of the study sites. However, impacts were significantly greater at a forest margin, where possum abundance was highest, and at a high-altitude site where mistletoe density was lowest. Mistletoe crown dieback was inversely proportional to intensity of possum browsing. These results suggest that the persistence of abundant mistletoe populations at these sites is due to mistletoe productivity matching or exceeding consumption by possums in these forests of low possum-carrying _______________________________________________________________________________________________________________________________capacity, rather than low possum preference for the local mistletoe populations. -
The Responses of New Zealand's Arboreal Forest Birds to Invasive
The responses of New Zealand’s arboreal forest birds to invasive mammal control Nyree Fea 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 Te Whare Wānanga o te Ūpoko o te Ika a Māui 2018 ii This thesis was conducted under the supervision of Dr. Stephen Hartley (primary supervisor) School of Biological Sciences Victoria University of Wellington Wellington, New Zealand and Associate Professor Wayne Linklater (secondary supervisor) School of Biological Sciences Victoria University of Wellington Wellington, New Zealand iii iv Abstract Introduced mammalian predators are responsible for over half of contemporary extinctions and declines of birds. Endemic bird species on islands are particularly vulnerable to invasions of mammalian predators. The native bird species that remain in New Zealand forests continue to be threatened by predation from invasive mammals, with brushtail possums (Trichosurus vulpecula) ship rats (Rattus rattus) and stoats (Mustela erminea) identified as the primary agents responsible for their ongoing decline. Extensive efforts to suppress these pests across New Zealand’s forests have created “management experiments” with potential to provide insights into the ecological forces structuring forest bird communities. To understand the effects of invasive mammals on birds, I studied responses of New Zealand bird species at different temporal and spatial scales to different intensities of control and residual densities of mammals. In my first empirical chapter (Chapter 2), I present two meta-analyses of bird responses to invasive mammal control. I collate data from biodiversity projects across New Zealand where long-term monitoring of arboreal bird species was undertaken. -
Co-Extinction of Mutualistic Species – an Analysis of Ornithophilous Angiosperms in New Zealand
DEPARTMENT OF BIOLOGICAL AND ENVIRONMENTAL SCIENCES CO-EXTINCTION OF MUTUALISTIC SPECIES An analysis of ornithophilous angiosperms in New Zealand Sandra Palmqvist Degree project for Master of Science (120 hec) with a major in Environmental Science ES2500 Examination Course in Environmental Science, 30 hec Second cycle Semester/year: Spring 2021 Supervisor: Søren Faurby - Department of Biological & Environmental Sciences Examiner: Johan Uddling - Department of Biological & Environmental Sciences “Tui. Adult feeding on flax nectar, showing pollen rubbing onto forehead. Dunedin, December 2008. Image © Craig McKenzie by Craig McKenzie.” http://nzbirdsonline.org.nz/sites/all/files/1200543Tui2.jpg Table of Contents Abstract: Co-extinction of mutualistic species – An analysis of ornithophilous angiosperms in New Zealand ..................................................................................................... 1 Populärvetenskaplig sammanfattning: Samutrotning av mutualistiska arter – En analys av fågelpollinerade angiospermer i New Zealand ................................................................... 3 1. Introduction ............................................................................................................................... 5 2. Material and methods ............................................................................................................... 7 2.1 List of plant species, flower colours and conservation status ....................................... 7 2.1.1 Flower Colours ............................................................................................................. -
Mistletoe Effects on Acacia Species in Western Saudi Arabia Dhafer Albakre
Mistletoe effects on acacia species in western Saudi Arabia Dhafer Albakre Thesis submitted for the degree of a Doctor of Philosophy School of Biological Sciences The University of Adelaide South Australia April 2019 Table of Contents Declaration ......................................................................................................................................................... 3 Acknowledgments .............................................................................................................................................. 4 Abstract .............................................................................................................................................................. 7 Chapter 1: General introduction ..................................................................................................................... 11 Identification of mistletoes ............................................................................................................. 13 Life history .................................................................................................................................... 13 The effects of mistletoes on their hosts ........................................................................................... 14 Physiological effects ...................................................................................................................... 17 Effects on individuals .................................................................................................................... -
Eocene Loranthaceae Pollen Pushes Back Divergence Ages for Major Splits in the Family
Eocene Loranthaceae pollen pushes back divergence ages for major splits in the family Friðgeir Grı´msson1,*, Paschalia Kapli2, Christa-Charlotte Hofmann1, Reinhard Zetter1 and Guido W. Grimm1,3,* 1 Department of Palaeontology, University of Vienna, Wien, Austria 2 The Exelixis Lab, Scientific Computing Group, Heidelberg Institute for Theoretical Studies, Heidelberg, Germany 3 Orle´ans, France * These authors contributed equally to this work. ABSTRACT Background: We revisit the palaeopalynological record of Loranthaceae, using pollen ornamentation to discriminate lineages and to test molecular dating estimates for the diversification of major lineages. Methods: Fossil Loranthaceae pollen from the Eocene and Oligocene are analysed and documented using scanning-electron microscopy. These fossils were associated with molecular-defined clades and used as minimum age constraints for Bayesian node dating using different topological scenarios. Results: The fossil Loranthaceae pollen document the presence of at least one extant root-parasitic lineage (Nuytsieae) and two currently aerial parasitic lineages (Psittacanthinae and Loranthinae) by the end of the Eocene in the Northern Hemisphere. Phases of increased lineage diversification (late Eocene, middle Miocene) coincide with global warm phases. Discussion: With the generation of molecular data becoming easier and less expensive every day, neontological research should re-focus on conserved 16 December 2016 Submitted morphologies that can be traced through the fossil record. The pollen, representing Accepted 4May2017 Published 7 June 2017 the male gametophytic generation of plants and often a taxonomic indicator, can be such a tracer. Analogously, palaeontological research should put more effort Corresponding authors Friðgeir Grı´msson, into diagnosing Cenozoic fossils with the aim of including them into modern [email protected] systematic frameworks. -
Inflorescence and Floral Traits of the Colombian Species of Tristerix (Loranthaceae) Related to Hummingbird Pollination
Anales del Jardín Botánico de Madrid 74 (2): e061 http://dx.doi.org/10.3989/ajbm.2474 ISSN: 0211-1322 [email protected], http://rjb.revistas.csic.es/index.php/rjb Copyright: © 2017 CSIC. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial (by-nc) Spain 3.0 License. Inflorescence and floral traits of the Colombian species of Tristerix (Loranthaceae) related to hummingbird pollination Favio González 1,* & Natalia Pabón-Mora 2 1 Facultad de Ciencias, Instituto de Ciencias Naturales, Universidad Nacional de Colombia, AA 7495 Bogotá, Colombia 2 Instituto de Biología, Universidad de Antioquia, AA 1226 Medellín, Colombia * Corresponding author: [email protected], http://orcid.org/0000-0001-5716-9278 2 [email protected], http://orcid.org/0000-0003-3528-8078 Abstract. Floral diversification in Loranthaceae reaches its highest peak Resumen. La diversificación floral en Loranthaceae alcanza su máxima in the Andes. The flowers of the exclusively Andean genusTristerix exhibit expresión en los Andes. Las flores del género Tristerix, restringido tubular and vividly coloured flowers pollinated by hummingbirds. We exclusivamente a dicha cordillera, exhiben flores tubulares y de color llamativo que son polinizadas por colibríes. Se ha realizado un estudio de la studied inflorescence and flower morphoanatomy of the two Colombian morfoanatomía de inflorescencias y flores en las dos especies colombianas species, T. longebracteatus and the highly endangered T. secundus. Both del género, T. longebracteatus y T. secundus, esta última muy amenazada. species have terminal racemes with up to 26 ebracteolate flowers, of Las dos especies tienen racimos terminales hasta con 26 flores ebracteoladas, which the proximal one opens and sets fruits first. -
Restoration Planting in Taranaki
CONTENTS Part one: Getting started Introduction .................................................................... 2 Ecological Regions and Districts of Taranaki .................... 3 Plan of Action ................................................................. 4 Part two: Target ecosystems Vegetation patterns .........................................................9 What to plant and where ...............................................11 Coastal Spinifex duneland ..........................................................13 Harakeke–raupo–kuta wetland .......................................14 Saltmarsh ribbonwood–oioi estuary shrubland ..............15 Taupata–kawakawa–harakeke/wharariki shrubland ........16 Coastal herbfield ...........................................................17 Tainui forest ...................................................................18 Karaka-tawa–puriri forest ...............................................19 Coastal–semi-coastal Kahikatea–pukatea swamp/semi-swamp forest .......... 21 Kohekohe–karaka–puriri forest .......................................22 Semi-coastal–lowland Manuka–Gaultheria–wharariki shrubland .......................23 Tawa forest .....................................................................24 Tawa–pukatea forest ......................................................25 Lowland Tawa–kamahi forest .......................................................27 Hard beech and black beech forest ................................28 Waitaanga area silver beech–kamahi forest....................29 -
A Revised Classification of Santalales
Vol. 59 • February 2010 TAXON 59 (2) • April 2010: 1–1 Nickrent & al. • Classification of Santalales International Journal of Taxonomy, Phylogeny and Evolution Electronic Supplement to A revised classification of Santalales Daniel L. Nickrent, Valéry Malécot, Romina Vidal-Russell & Joshua P. Der Taxon 59: pp–pp 1 TAXON 59 (2) • April 2010: Electronic Supplement, 3 pp. Nickrent & al. • Classification of Santalales CHROMOSOME NUMBERS FOR SANTALALES 10.3. Tribe Elytrantheae Chromosome numbers were reported for Alepis flavida, 1. Family Erythropalaceae Amylotheca (two species), Decaisnina (three species), and Ely- Chromosome numbers have been reported for Heiste- tranthe capitellata by Bir & al. (1982), for Elytranthe parasitica ria parvifolia pollen mother cells and pollen (Mangenot & (Soman & Ramachandran, 1987), as well as the following from Mangenot, 1958): n = 16. Barlow & Wiens (1971): Lepeostegeres gemmiflorus, Lysiana (five species), Macrosolen (two species; for two additional spe- 2. Family Strombosiaceae cies see Sanjappa, 1979; Sarkar & Datta, 1990), and Peraxilla Chromosome numbers have been reported from root cells tetrapeta and all are n = 12. of Strombosia glaucescens var. lucida (Mangenot & Mangenot, 1958): n = 20 (also 40, likely from endopolyploidy). 10.4. Tribe Psittacantheae 3. Family Coulaceae 10.4.1. Subtribe Tupeinae No chromosome numbers have been reported. The chromosome number for Tupeia antarctica originally reported as n = 11 by Barlow & Wiens (1971) was erroneous 4. Family Ximeniaceae and later corrected to n = 12 (Beuzenberg & Groves, 1974). Chromosome numbers have been reported for Malania oleifera (Yang & al., 2003): n = 13; Ximenia americana (Rob- 10.4.2. Subtribe Notantherinae ertson, 1982; Hunziker & al., 1985): n = 13, 26. Kondo & al. Chromosome numbers, both from Barlow & Wiens (1971), (1981) reported slightly different numbers for that species: are as follows: Desmaria mutabilis n = 16–18, Notanthera het- n = 12, 24.