Macrofossils and Pollen Representing Forests of the Pre-Taupo Volcanic Eruption (C
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A Commentary on Canopy Tree Mortality in Westland Rata-Kamahi Protection Forests G
A COMMENTARY ON CANOPY TREE MORTALITY IN WESTLAND RATA-KAMAHI PROTECTION FORESTS G. H. STEWART* and T. T. VEBLEN f ABSTRACT The apparently excessive canopy tree mortality in the rata- kamahi forests of Westland has resulted in the widespread belief that persistence of the forest cover in this area may be endangered. Browsing by the Australian brush-tailed possum (Trichosurus , vulpecula) is commonly believed to be the cause of the widespread mortality. Consequently', research has been directed towards studies of possum diet and vegetation condition under varying possum densities. However, browsing by possums does not appear to be the sole cause of the tree mortality. Natural stand dynamic processes appear to contribute importantly to the observed mortality patterns. The development of even-aged stands following massive disturbances such as mass movements and windthrow and, thus, the presence of groups of senescent trees appears to be an important contributory factor. Possum browsing (as well as other lethal influences) may be affecting stands already susceptible as a result of natural stand dynamic processes. INTRODUCTION Grey crowns of dead or apparently dying trees are often conspicuous in the highland hardwood-softwood forests of the North and South Islands of New Zealand. They are especially common in rata-kamahi forests in Westland, on the South Island, where in many areas they give a white tint to the landscape. Since the 1940s this mortality has caused concern as these rata- kamahi forests are considered vital to the protection of agricultural and forestry production in the adjacent lowlands. •Protection Forestry Division, Forest Research Institute, P.O. -
Researchcommons.Waikato.Ac.Nz
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Research Commons@Waikato 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. Identifying Host Species of Dactylanthus taylorii using DNA Barcoding A thesis submitted in partial fulfilment of the requirements for the degree of Masters of Science in Biological Sciences at The University of Waikato by Cassarndra Marie Parker _________ The University of Waikato 2015 Acknowledgements: This thesis wouldn't have been possible without the support of many people. Firstly, my supervisors Dr Chrissen Gemmill and Dr Avi Holzapfel - your professional expertise, advice, and patience were invaluable. From pitching the idea in 2012 to reading through drafts in the final fortnight, I've been humbled to work with such dedicated and accomplished scientists. Special mention also goes to Thomas Emmitt, David Mudge, Steven Miller, the Auckland Zoo horticulture team and Kevin. -
Araliaceae) Roderick J
Essential Oils from the Leaves of Three New Zealand Species of Pseudopanax (Araliaceae) Roderick J. Weston Industrial Research Ltd., P.O. Box 31-310, Lower Hutt, New Zealand. Fax: +64-4-9313-055. E-mail: [email protected] Z. Naturforsch. 59c, 39Ð42 (2004); received July 22, 2003 Essential oils from three of the eleven endemic New Zealand species of Pseudopanax, P. arboreus, P. discolor and P. lessonii, were found to have a fairly uniform composition which was different from that of the oils of Raukaua species that were formerly classified in the Pseudopanax genus. Oils of the three Pseudopanax species all contained significant propor- tions of viridiflorol and a closely related unidentified hydroazulene alcohol in common. In addition, the oil of P. arboreus contained bicyclogermacrene, linalool and long chain hy- drocarbons. The oil of P. discolor contained nerolidol in abundance (36.3%) together with linalool and epi-α-muurolol. The oil of P. lessonii contained a complex mixture of sesquiter- pene alcohols including epi-α-muurolol and a mixture of long chain hydrocarbons. Nerolidol and linalool provided the oil of P. discolor with a pleasant floral aroma, but the yield of oil was very low (0.01%). Key words: Pseudopanax arboreus, discolor and lessonii, Araliaceae, Essential Oil Introduction species studied in this paper, P. lessonii and P. dis- color, belong to this group and were selected be- The Araliaceae is a family of 65 genera and ap- cause their leaves, when crushed, emit a weak fra- proximately 800 species, which occur mainly in grance. The third group is characterized by its tropical regions, but some genera are found in shorter wider fleshier leaves and includes P. -
Nzbotsoc No 86 Dec 2006
NEW ZEALAND BOTANICAL SOCIETY NEWSLETTER NUMBER 86 DECEMBER 2006 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 8001 Subscriptions The 2006 ordinary and institutional subscriptions are $25 (reduced to $18 if paid by the due date on the subscription invoice). The 2006 student subscription, 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 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 March 2007 issue is 25 February 2007 Please post contributions to: Melanie Newfield 17 Homebush Rd Khandallah Wellington Send email contributions to [email protected]. Files are preferably in MS Word (Word XP or earlier) or saved as RTF or ASCII. -
Patterns of Flammability Across the Vascular Plant Phylogeny, with Special Emphasis on the Genus Dracophyllum
Lincoln University Digital Thesis Copyright Statement The digital copy of this thesis is protected by the Copyright Act 1994 (New Zealand). This thesis may be consulted by you, provided you comply with the provisions of the Act and the following conditions of use: you will use the copy only for the purposes of research or private study 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. Patterns of flammability across the vascular plant phylogeny, with special emphasis on the genus Dracophyllum A thesis submitted in partial fulfilment of the requirements for the Degree of Doctor of philosophy at Lincoln University by Xinglei Cui Lincoln University 2020 Abstract of a thesis submitted in partial fulfilment of the requirements for the Degree of Doctor of philosophy. Abstract Patterns of flammability across the vascular plant phylogeny, with special emphasis on the genus Dracophyllum by Xinglei Cui Fire has been part of the environment for the entire history of terrestrial plants and is a common disturbance agent in many ecosystems across the world. Fire has a significant role in influencing the structure, pattern and function of many ecosystems. Plant flammability, which is the ability of a plant to burn and sustain a flame, is an important driver of fire in terrestrial ecosystems and thus has a fundamental role in ecosystem dynamics and species evolution. However, the factors that have influenced the evolution of flammability remain unclear. -
A Quantitative Assessment of Shoot Flammability for 60 Tree and Shrub Species Supports Rankings Based on Expert Opinion
CSIRO PUBLISHING International Journal of Wildland Fire 2016, 25, 466–477 http://dx.doi.org/10.1071/WF15047 A quantitative assessment of shoot flammability for 60 tree and shrub species supports rankings based on expert opinion Sarah V. WyseA,B,G, George L. W. PerryA,C, Dean M. O’ConnellD, Phillip S. HollandD, Monique J. WrightD, Catherine L. HostedD,E, Samuel L. WhitelockD, Ian J. GearyD,F, Ke´vinJ.L.MaurinD and Timothy J. CurranD ASchool of Environment, University of Auckland, Private Bag 92019 Auckland 1142, New Zealand. BRoyal Botanic Gardens Kew, Wakehurst Place, RH17 6TN, UK. CSchool of Biological Sciences, University of Auckland, Private Bag 92019 Auckland 1142, New Zealand. DEcology Department, Lincoln University, PO Box 85084, Lincoln 7647, Canterbury, New Zealand. EWai-Ora Forest Landscapes Ltd, 48 Watsons Road, Harewood 8051, Christchurch, New Zealand. FDepartment of Geology, University of Otago, PO Box 56 Dunedin 9054, New Zealand. GCorresponding author. Email: [email protected] Abstract. Fire is an important ecological disturbance in vegetated ecosystems across the globe, and also has considerable impacts on human infrastructure. Vegetation flammability is a key bottom-up control on fire regimes and on the nature of individual fires. Although New Zealand (NZ) historically had low fire frequencies, anthropogenic fires have considerably impacted indigenous vegetation as humans used fire extensively to clear forests. Few studies of vegetation flammability have been undertaken in NZ and only one has compared the flammability of indigenous plants; this was a qualitative assessment derived from expert opinion. We addressed this knowledge gap by measuring the flammability of terminal shoots from a range of trees and shrubs found in NZ. -
Forests and Scrublands of Northern Fiordland
80 Vol. 1 FORESTS AND SCRUBLANDS OF NORTHERN FIORDLAND J. WARDLE, J. HAYWARD, and J. HERBERT, Forest and Range Experiment Station, New Zealand Forest Service, Rangiora (Received for publication 18 January 1971) ABSTRACT The composition and structure of the forests and scrublands of northern Fiordland were recorded at 1,053 sample points. The vegetation at each sample point was classified into one of 16 associations using a combination of Sorensen's 'k' index of similarity, and a multi-linkage cluster analysis. The associations were related to habitat and the distribution of each was determined. The influence of the introduced ungulates, red deer and wapiti, on the forests and scrublands was determined. Stand structure was analysed to provide infor mation on the susceptibility of the vegetation to damage from browsing and on the history of ungulate utilisation of the vegetation. Browse indices were calculated to provide information on current ungulate utilisation of the vegetation. INTRODUCTION A reconnaissance of northern Fiordland was carried out during the summer of 1969-70 by staff of the Forest and Range Experiment Station. The purpose was to describe the composition, structure, and habitat of the forest and scrub associations, to determine both present and past influence of ungulates on them, and to establish a number of permanent reference points to permit measurement of future changes in the vegetation. The area studied lies between the western shores of Lake Te Anau and the Tasman Sea. The southern boundary is the South Fiord of Lake Te Anau, the Esk Burn and Windward River catchments, and Charles Sound; the northern boundary is the Worsley and Transit River catchments (Fig. -
The Island Rule and Its Application to Multiple Plant Traits
The island rule and its application to multiple plant traits Annemieke Lona Hedi Hendriks A thesis submitted to the Victoria University of Wellington in partial fulfilment of the requirements for the degree of Master of Science in Ecology and Biodiversity Victoria University of Wellington, New Zealand 2019 ii “The larger the island of knowledge, the longer the shoreline of wonder” Ralph W. Sockman. iii iv General Abstract Aim The Island Rule refers to a continuum of body size changes where large mainland species evolve to become smaller and small species evolve to become larger on islands. Previous work focuses almost solely on animals, with virtually no previous tests of its predictions on plants. I tested for (1) reduced floral size diversity on islands, a logical corollary of the island rule and (2) evidence of the Island Rule in plant stature, leaf size and petiole length. Location Small islands surrounding New Zealand; Antipodes, Auckland, Bounty, Campbell, Chatham, Kermadec, Lord Howe, Macquarie, Norfolk, Snares, Stewart and the Three Kings. Methods I compared the morphology of 65 island endemics and their closest ‘mainland’ relative. Species pairs were identified. Differences between archipelagos located at various latitudes were also assessed. Results Floral sizes were reduced on islands relative to the ‘mainland’, consistent with predictions of the Island Rule. Plant stature, leaf size and petiole length conformed to the Island Rule, with smaller plants increasing in size, and larger plants decreasing in size. Main conclusions Results indicate that the conceptual umbrella of the Island Rule can be expanded to plants, accelerating understanding of how plant traits evolve on isolated islands. -
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. -
A Phylogeny of the Flowering Plant
American Journal of Botany 87(2): 273±292. 2000. A PHYLOGENY OF THE FLOWERING PLANT FAMILY APIACEAE BASED ON CHLOROPLAST DNA RPL16 AND RPOC1 INTRON SEQUENCES: TOWARDS A SUPRAGENERIC CLASSIFICATION OF SUBFAMILY APIOIDEAE1 STEPHEN R. DOWNIE,2,4 DEBORAH S. KATZ-DOWNIE,2 AND MARK F. W ATSON3 2Department of Plant Biology, University of Illinois, Urbana, Illinois 61801 USA; and 3Royal Botanic Garden Edinburgh, 20A Inverleith Row, Edinburgh EH3 5LR, Scotland, UK The higher level relationships within Apiaceae (Umbelliferae) subfamily Apioideae are controversial, with no widely acceptable modern classi®cation available. Comparative sequencing of the intron in chloroplast ribosomal protein gene rpl16 was carried out in order to examine evolutionary relationships among 119 species (99 genera) of subfamily Apioideae and 28 species from Apiaceae subfamilies Saniculoideae and Hydrocotyloideae, and putatively allied families Araliaceae and Pittosporaceae. Phylogenetic analyses of these intron sequences alone, or in conjunction with plastid rpoC1 intron sequences for a subset of the taxa, using maximum parsimony and neighbor-joining methods, reveal a pattern of relationships within Apioideae consistent with previously published chloroplast DNA and nuclear ribosomal DNA ITS based phylogenies. Based on consensus of relationship, seven major lineages within the subfamily are recognized at the tribal level. These are referred to as tribes Heteromorpheae M. F. Watson & S. R. Downie Trib. Nov., Bupleureae Spreng. (1820), Oenantheae Dumort. (1827), Pleurospermeae M. F. Watson & S. R. Downie Trib. Nov., Smyrnieae Spreng. (1820), Aciphylleae M. F. Watson & S. R. Downie Trib. Nov., and Scandiceae Spreng. (1820). Scandiceae comprises subtribes Daucinae Dumort. (1827), Scan- dicinae Tausch (1834), and Torilidinae Dumort. (1827). -
Environmental Pest Plants
RESTORATION PLAN FOR THE SPENCER ROAD PART OF THE LAKE TARAWERA CATCHMENT R4152c RESTORATION PLAN FOR THE SPENCER ROAD PART OF THE LAKE TARAWERA CATCHMENT Contract Report No. 4152c February 2017 Updated February 2019 Project Team: Richard Gillies - Fieldwork, report author Jennifer Murray - Fieldwork, report author Sarah Beadel - Field assessment, project management, report author, peer review Prepared for: Lake Tarawera Ratepayers Association and Tarawera Landcare 2115 99 SALA STREET, WHAKAREWAREWA, 3010, P.O. BOX 7137, TE NGAE, ROTORUA 3042 Ph 07-343-9017; Fax 07-343-9018, email [email protected], www.wildlands.co.nz EXECUTIVE SUMMARY Tarawera Landcare 2115, via the Lake Tarawera Ratepayers Association, has signed a MoU with Rotorua Lakes Council regarding the management of Council land along the margins of Lake Tarawera between Otumutu Lagoon and Te Toroa Point. The site is c.6.5 km long and covers 24 ha. The Lake Tarawera Ratepayers Association has commissioned this plan to guide ecological management there. A separate plan has been developed for Māori land on Kariri Point. A review of background information and ecological surveys and assessments of the study area were undertaken during October-December 2016. Indigenous forest dominated by māhoe, mamaku, kāmahi, fivefinger and, in places, pōhutukawa and kānuka, occupies around 40% of the study area, and is representative of the vegetation regenerating after the 1886 Tarawera eruption. A distinctive feature is the presence of healthy numbers of the mistletoe Tupeia antarctica, an At Risk species, from Cliff Road Reserve northwards, attributable to ongoing possum control by the Tarawera community. Lakeshore vegetation provides roosting and nesting habitat for waterbirds, particularly dabchick, a Threatened endemic waterbird present along the entire shoreline. -
Low Fruit Set, Pollen Limitation and the Roles of Birds and Insects in Pollination of Native New Zealand Plants
1 Low Fruit Set, Pollen Limitation and the Roles of Birds and Insects in Pollination of Native New Zealand Plants. A thesis submitted in partial fulfilment of the requirements for the Degree of Master of Science in Zoology in the University of Canterbury by Cassandra J Greenfield University of Canterbury December 2010 2 Table of Contents Abstract ............................................................................................................................................. 4 Chapter One: An introduction to pollen limitation .............................................................................. 5 1.1 Introduction ............................................................................................................................. 5 1.2 The New Zealand situation....................................................................................................... 6 1.3 Distinguishing between the hypotheses .................................................................................. 15 1.4 Focus of study ....................................................................................................................... 23 Chapter Two: Cordyline australis .................................................................................................... 25 2.1 Introduction ........................................................................................................................... 25 2.2 Materials and methods ..........................................................................................................