Threatened Plants of Waikato Conservancy
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The Vegetation of Robinson Crusoe Island (Isla Masatierra), Juan
The Vegetation ofRobinson Crusoe Island (Isla Masatierra), Juan Fernandez Archipelago, Chile1 Josef Greimler,2,3 Patricio Lopez 5., 4 Tod F. Stuessy, 2and Thomas Dirnbiick5 Abstract: Robinson Crusoe Island of the Juan Fernandez Archipelago, as is the case with many oceanic islands, has experienced strong human disturbances through exploitation ofresources and introduction of alien biota. To understand these impacts and for purposes of diversity and resource management, an accu rate assessment of the composition and structure of plant communities was made. We analyzed the vegetation with 106 releves (vegetation records) and subsequent Twinspan ordination and produced a detailed colored map at 1: 30,000. The resultant map units are (1) endemic upper montane forest, (2) endemic lower montane forest, (3) Ugni molinae shrubland, (4) Rubus ulmifolius Aristotelia chilensis shrubland, (5) fern assemblages, (6) Libertia chilensis assem blage, (7) Acaena argentea assemblage, (8) native grassland, (9) weed assemblages, (10) tall ruderals, and (11) cultivated Eucalyptus, Cupressus, and Pinus. Mosaic patterns consisting of several communities are recognized as mixed units: (12) combined upper and lower montane endemic forest with aliens, (13) scattered native vegetation among rocks at higher elevations, (14) scattered grassland and weeds among rocks at lower elevations, and (15) grassland with Acaena argentea. Two categories are included that are not vegetation units: (16) rocks and eroded areas, and (17) settlement and airfield. Endemic forests at lower elevations and in drier zones of the island are under strong pressure from three woody species, Aristotelia chilensis, Rubus ulmifolius, and Ugni molinae. The latter invades native forests by ascending dry slopes and ridges. -
New Exotic Host for the Dwarf Mistletoe Korthalsella Salicornioides
TRILEPIDEA Newsletter of the New Zealand Plant Conservation Network NO. 201 New exotic host for the dwarf mistletoe Korthalsella salicornioides August 2020 John Barkla ([email protected]) Deadline for next issue: On 16 August 2020, while walking Friday 16 September 2020 the Abel Tasman Coastal Track, I SUBMIT AN ARTICLE observed and photographed the dwarf TO THE NEWSLETTER mistletoe Korthalsella salicornioides Contributions are welcome [Viscaceae] hemiparasitic on its gorse to the newsletter at any (Ulex europaeus [Fabaceae]) host. One time. The closing date for gorse shrub was observed hosting articles for each issue is approximately the 15th of several large plants of Korthalsella each month. salicornioides (Fig. 1). Articles may be edited and used in the newsletter and/ Th e site is on gentle hill country, or on the website news page. approximately 60 metres above sea Figure 1. Korthalsella salicornioides hemiparasitic on The Network will publish level and located about halfway gorse. Abel Tasman National Park, 16 August 2020. almost any article about between Th e Anchorage and Watering Photo: John Barkla. plants and plant conservation Cove. Trackside vegetation here comprises coastal shrubland dominated by kanuka with a particular focus on the plant life of New Zealand and (Kunzea ericoides) with manuka (Leptospermum scoparium) and prickly mingimingi Oceania. (Leptocophylla juniperina subsp. juniperina) both common. Gorse is sporadically Please send news items present, occupying otherwise bare ground that may be a result of the track’s or event information to construction and maintenance. [email protected] Postal address: Korthalsella salicornioides was abundant on host kanuka growing in close proximity c/- 160 Wilton Road to the gorse shrub host. -
Temporal Development and Regeneration Dynamics of Restored Urban Forests
Temporal Development and Regeneration Dynamics of Restored Urban Forests By Katherine de Silva A thesis submitted to the Victoria University of Wellington in fulfilment of the requirements for the degree of Masters in Ecology & Biodiversity School of Biological Sciences Faculty of Sciences Victoria University of Wellington October 2019 Supervisors: Stephen Hartley. Director of the Centre of Biodiversity & Restoration Ecology, Victoria University of Wellington Kiri Joy Wallace. Postdoctoral Fellow, Environmental Research Institute, University of Waikato. Katherine de Silva: Temporal Development and Regeneration Dynamics of Restored Urban Forests, © October 2019. 2 ABSTRACT Urban forest restoration programmes are a key tool used to initiate, re-create or accelerate the succession of forest species; improving ecosystem services, function, resilience and biodiversity. Succession is a temporal shift in species dominance driven by abiotic and biotic influences, but over decadal timescales the trajectory and success of restoration plantings in degraded urban environments can be hindered. To facilitate the successful reconstruction of forest ecosystems from scratch, an understanding of the temporal patterns in planted forest development, dynamics of seedling regeneration and dominant drivers of seedling diversity is required. Using a chronosequence approach, permanent plots were established at 44 restored urban forests aged 5 to 59 years since initial plantings took place, across five New Zealand cities between Wellington and Invercargill. Vegetation surveys were undertaken and data on micro- climate were collected. This study examined the 1) temporal dynamics of restored urban forest development and seedling regeneration and 2) dominant drivers of seedling regeneration. Data were analysed using linear regression models, breakpoint analysis and mixed-effects modelling. Early forest development (<20 years) exhibited the most changes in canopy composition and structure, forest floor dynamics, seedling community and microclimate. -
Threatened Plants of Waikato Conservancy
Austrofestuca littoralis hinarepe, sand tussock POACEAE Status Gradual Decline Description A stout, tufted, erect grass forming pale yellow-green tussocks, to 1 m tall. The leaves are fine, rolled and needle-like. Seed heads are buried within foliage, are flattened, yellowish-white and have a zigzag appearance. Similar species Marram has larger blue-green leaves and is a much more robust plant. Current record The catstail-like seed heads of marram are considerably more crowded Historic record and are held above the foliage. Extinct Habitat Sandy beaches, though it occasionally grows on damp sand on coastal Austrofestuca littoralis habitat. stream margins. Photo: S.P. Courtney. Distribution Australia, where very common and New Zealand. In New Zealand locally distributed on North, South, and Stewart Islands, apparently now extinct on the Chatham Islands (Walls et al. 2003). In the Waikato it is known from a couple of eastern Coromandel beaches, and at one site on the west coast near Kawhia. Threats Exact cause of past decline has not been established, though sand tussock is palatable to cattle and horses, and it is thought to have been displaced by marram grass (Ammophila arenaria). Sand tussock is also vulnerable to trampling and vehicle disturbance and so has declined in the vicinity of many coastal resorts. 15 Austrofestuca littoralis. Photo: B. Mitcalfe. Austrofestuca littoralis. Illustration by C. Beard. 16 Brachyglottis kirkii var. kirkii Kirk’s daisy ASTERACEAE Status Serious Decline Description A spring flowering, usually epiphytic shrub to 1.5 m tall with purple stems and grey bark developed on old wood. Leaves 40–100 × 20– 40 mm, fleshy or variable in shape, usually toothed in upper third, hairless, upper surface pale to dark green, often tinged maroon, undersides paler. -
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. -
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY BIBLIOGRAPHY Ackerfield, J., and J. Wen. 2002. A morphometric analysis of Hedera L. (the ivy genus, Araliaceae) and its taxonomic implications. Adansonia 24: 197-212. Adams, P. 1961. Observations on the Sagittaria subulata complex. Rhodora 63: 247-265. Adams, R.M. II, and W.J. Dress. 1982. Nodding Lilium species of eastern North America (Liliaceae). Baileya 21: 165-188. Adams, R.P. 1986. Geographic variation in Juniperus silicicola and J. virginiana of the Southeastern United States: multivariant analyses of morphology and terpenoids. Taxon 35: 31-75. ------. 1995. Revisionary study of Caribbean species of Juniperus (Cupressaceae). Phytologia 78: 134-150. ------, and T. Demeke. 1993. Systematic relationships in Juniperus based on random amplified polymorphic DNAs (RAPDs). Taxon 42: 553-571. Adams, W.P. 1957. A revision of the genus Ascyrum (Hypericaceae). Rhodora 59: 73-95. ------. 1962. Studies in the Guttiferae. I. A synopsis of Hypericum section Myriandra. Contr. Gray Herbarium Harv. 182: 1-51. ------, and N.K.B. Robson. 1961. A re-evaluation of the generic status of Ascyrum and Crookea (Guttiferae). Rhodora 63: 10-16. Adams, W.P. 1973. Clusiaceae of the southeastern United States. J. Elisha Mitchell Sci. Soc. 89: 62-71. Adler, L. 1999. Polygonum perfoliatum (mile-a-minute weed). Chinquapin 7: 4. Aedo, C., J.J. Aldasoro, and C. Navarro. 1998. Taxonomic revision of Geranium sections Batrachioidea and Divaricata (Geraniaceae). Ann. Missouri Bot. Gard. 85: 594-630. Affolter, J.M. 1985. A monograph of the genus Lilaeopsis (Umbelliferae). Systematic Bot. Monographs 6. Ahles, H.E., and A.E. -
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. -
Dessication Response of Seed of Clianthus Spp., Carmichaelia Muritai, Pittosporum Crassifolium and Pittosporum Eugenoides
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. Desiccation response of seed of Clianthus spp., Carmichaelia muritai, Pittosporum crassifolium and Pittosporum eugenioides A thesis presented in partial fulfilment of the requirements for the degree of Master of AgriScience in Horticulture at Massey University, Palmerston North, New Zealand Kai Yu 2015 ABSTRACT New Zealand has a rich, diverse and unique of plant life. However, the conservation status of the New Zealand indigenous vascular flora is deteriorating, with 7.6% of this flora regarded as threatened with extinction. A series of conservation approaches are required to protect species against further loss. Developing ex-situ conservation of these species requires basic information such as seed storage behaviour and seed germination requirements to be determined. However, for many species this information is missing or incomplete. The objective of this study was to determine seed storage behaviour (response to desiccation), and/or seed coat characteristics in selected New Zealand native species. Five native tree and shrub species were studied: Carmichaelia muritai, Clianthus puniceus, Clianthus maximus, Pittosporum eugenioides, and Pittosporum crassifolium. Seeds of Clianthus maximus, Clianthus puniceus, and Carmichaelia muritai were found desiccation tolerant at low moisture content (down to ~2.5%), suggesting the storage behaviour is orthodox; storage trials need to be conducted to confirm this. In contrast, the storage behaviour of Pittosporum eugenioides and Pittosporum crassifolium appears to be non-orthodox since there was some loss of viability upon drying to low moisture contents. -
Supporting Information
Supporting Information Mao et al. 10.1073/pnas.1114319109 SI Text BEAST Analyses. In addition to a BEAST analysis that used uniform Selection of Fossil Taxa and Their Phylogenetic Positions. The in- prior distributions for all calibrations (run 1; 144-taxon dataset, tegration of fossil calibrations is the most critical step in molecular calibrations as in Table S4), we performed eight additional dating (1, 2). We only used the fossil taxa with ovulate cones that analyses to explore factors affecting estimates of divergence could be assigned unambiguously to the extant groups (Table S4). time (Fig. S3). The exact phylogenetic position of fossils used to calibrate the First, to test the effect of calibration point P, which is close to molecular clocks was determined using the total-evidence analy- the root node and is the only functional hard maximum constraint ses (following refs. 3−5). Cordaixylon iowensis was not included in in BEAST runs using uniform priors, we carried out three runs the analyses because its assignment to the crown Acrogymno- with calibrations A through O (Table S4), and calibration P set to spermae already is supported by previous cladistic analyses (also [306.2, 351.7] (run 2), [306.2, 336.5] (run 3), and [306.2, 321.4] using the total-evidence approach) (6). Two data matrices were (run 4). The age estimates obtained in runs 2, 3, and 4 largely compiled. Matrix A comprised Ginkgo biloba, 12 living repre- overlapped with those from run 1 (Fig. S3). Second, we carried out two runs with different subsets of sentatives from each conifer family, and three fossils taxa related fi to Pinaceae and Araucariaceae (16 taxa in total; 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. -
Vascular Plants of an Unclassified Islet, Cape Brett Peninsula, Northern New Zealand, by E.K. Cameron, P
TANE 28,1982 VASCULAR PLANTS OF AN UNCLASSIFIED ISLET, CAPE BRETT PENINSULA, NORTHERN NEW ZEALAND by E.K. Cameron Department of Botany, University of Auckland, Private Bag, Auckland SUMMARY Seventy indigenous and 2 adventive vascular plants taxa are recorded for the "unmodified" islet. Its botanical value exceeds its small size because of the modification of the adjacent Cape Brett Peninsula and nearby islands. INTRODUCTION The islet is situated only a few metres off the northern coastline of Cape Brett Peninsula (Fig. 1). This steep beehive-shaped greywacke islet, less than two hectares in area, supports an excellent cover of indigenous vegetation compared with the adjacent goat (Copra hircus) browsed mainland. Approximately thirty minutes was spent on the islet during a four day botanical survey of Cape Brett Peninsula carried out for the Department of Lands and Survey, Auckland, in June 1980 (Cameron 1980). Time permitted only a single south-west to north-east traverse, returning to the starting point via the north-west littoral. PLANT COMMUNITIES For ease of description four plant associations (Fig. 2) are recognised although it must be remembered that these are by no means distinct as they grade into one another. Area 1: Coastal Rock. The amount of coastal rock on the islet is proportional to the degree of wave exposure and thus the north-eastern side of the islet has the greatest amount of exposed rock. Plants such as Asplenium flaccidum ssp. haurakiense, Samolus repens and the shore lobelia (Lobelia anceps) are frequently found growing in cracks and crevices. Others found here include the N.Z. -
The Anatomy of the Bark of Libocedrus in New Zealand
IAWA Bulletin n.s., Vol. 6 (1),1985 23 THE ANATOMY OF THE BARK OF LlBOCEDRUS IN NEW ZEALAND by Lek-Lim Chan'" School of Forestry, University of Canterbury, Christchurch, New Zealand Summary The anatomy of the bark of Libocedrus bid southwards. In South Island it is also found in willii and L. plumosa, both indigenous to New lowland forests in the west. Libocedrus plumosa Zealand, is described. The phloem cell types in is also a tall tree and is found in lowland forest clude axial and ray parenchyma, sieve cells and from 35° to beyond 38° S in North Island and fibres. Fibres are of two types, thin-walled and between Collingwood and Westhaven (NW. Nel thick-walled. The ends of these fibres are most son) in South Island. ly blunt or abrupt. Minute crystals (crystal sand) were found in Terminology the radial walls of some axial parenchyma cells, 'Conducting phloem' refers to that part of sieve cells and fibres. Trabeculae were abun the phloem close to the vascular cambium where dant in the bark of L. bidwillii. sieve cells are still functioning in conduction, The walls of the phellem cells were very thin, and 'living bark' designates that part of the appearing flimsy. Phelloderm cells in L. plumo bark outside the vascular cambium up to and sa seem to undergo sclerification just prior to including the last-formed periderm. death, upon formation of a new periderm deep All other terms used for tissues of the bark er in the phloem. are in common usage (see IA WA, 1964; Society Key words: Bark anatomy, crystals, Libocedrus, of American Foresters, 1958).