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Table 5.8 – Descriptions of Priority Flora Recorded in the Project Area Species, Family and Rank Descriptio
Oakajee Port and Rail OPR Rail Proposal – Vegetation and Flora Assessment Table 5.8 – Descriptions of Priority Flora Recorded in the Project Area No of No of Plants Species, Family and Locations Description Typical Habitat Recorded by Distribution Photographs Rank Recorded by ecologia ecologia A dense, rounded shrub growing from 0.5 m to 2 m in height. Its phyllodes are erect and the yellow, globular flowers are produced from June to August. Acacia lineolata Mullewa, east of subsp. multilineata (Photograph on right by S.J. Patrick. Image used Mingenew, Arrino with the permission of the Western Australian Sandplains. 1 1 (FABACEAE) and the locality of Herbarium, Department of Environment and Yuna. Priority 1 Conservation (http://florabase.dec.wa.gov.au/help/copyright). Accessed on Thursday, 3 December 2009) and growth habit again (right) (Photography: ecologia). Chamelaucium sp. 73 km south of Yalgoo (Y. Chadwick A bushy low shrub to 1.5 m high. This species Yalgoo, near Blue 1816) produces white/pink/purple flowers during Granite outcrops. 2 3 Hills, along Morawa‐ (MYRTACEAE) August and September. Yalgoo Road, and Wurarga. Priority 1 An upright, leafless, semi‐succulent herb that grows to between 0.4 and 1 m, although it has been recorded as growing to 2 m. The stems are Robinson Ranges, Euphorbia light green, and have a bluish‐grey waxy light Sandstone and Mount Augustus sarcostemmoides covering. When broken a white sap is exuded quartzite hills but Station. Also East from the stems. The rarely present leaves are has been located 67 254 Chewing Ranges, (EUPHORBIACEAE) narrow, lanceolate, opposite and are held on flat plains at Mount Giles and Priority 1 horizontally. -
Insectivorous Plants”, He Showed That They Had Adaptations to Capture and Digest Animals
the Strange, the Ugly, and the Bizarre . carnivores, parasites, and mycotrophs . Plant Oddities - Carnivores, Parasites & Mycotrophs Of all the plants, the most bizarre, the least understood, but yet the most interesting are those plants that have unusual modes of nutrient uptake. Carnivore: Nepenthes Plant Oddities - Carnivores, Parasites & Mycotrophs Of all the plants, the most bizarre, the least understood, but yet the most interesting are those plants that have unusual modes of nutrient uptake. Parasite: Rafflesia Plant Oddities - Carnivores, Parasites & Mycotrophs Of all the plants, the most bizarre, the least understood, but yet the most interesting are those plants that have unusual modes of nutrient uptake. Things to focus on for this topic! 1. What are these three types of plants 2. How do they live - selection 3. Systematic distribution in general 4. Systematic challenges or issues 5. Evolutionary pathways - how did they get to what they are Mycotroph: Monotropa Plant Oddities - The Problems Three factors for systematic confusion and controversy 1. the specialized roles often involve reductions or elaborations in both vegetative and floral features — DNA also is reduced or has extremely high rates of change for example – the parasitic Rafflesia Plant Oddities - The Problems Three factors for systematic confusion and controversy 2. their connections to other plants or fungi, or trapping of animals, make these odd plants prone to horizontal gene transfer for example – the parasitic Mitrastema [work by former UW student Tom Kleist] -
Carnivorous Plant Newsletter V44 N4 December 2015
Technical Refereed Contribution Soil pH values at sites of terrestrial carnivorous plants in south-west Europe Lubomír Adamec • Institute of Botany of the Czech Academy of Sciences • Dukelská 135 • CZ-379 82 Trˇebonˇ • Czech Republic • [email protected] Keywords: Soil water pH, neutral soils, Pinguicula spp., Drosera intermedia, Drosophyllum lusitanicum. Abstract: Although the majority of terrestrial carnivorous plants grow in acidic soils at a pH of 3.5-5.5, there are many dozens of carnivorous species, mostly mountainous or rocky Pinguicula species, which grow preferen- tially or strictly in neutral or slightly alkaline soils at pHs between 7-8. Knowledge of an optimum soil pH value and an amplitude of this factor may be important not only for understanding the ecology of various species and their conservation, but also for successfully growing them. I report soil pH values at microsites of 15 terrestrial carnivorous plant species or subspecies in SW Europe. Introduction The majority of terrestrial carnivorous plants grow in wetlands such as peat bogs, fens, wet meadows, or wet clayish sands. The soils have usually low available mineral nutrient content (N, P, K, Ca, Mg), are hypoxic or anoxic and usually acidic (Juniper et al. 1989; Adamec 1997; Rice 2006). Unlike mineral nutritional character- istics of these soils, which have commonly been studied and related to carnivorous plant growth in the field or greenhouse experiments and which have also been published (for the review see Adamec 1997), relatively very little is known about the relationship between soil pH and growth of terrestrial carnivorous plants. Although some limited knowledge of soil pH at habitats of carnivorous plants or in typical substrates exist among botanists and growers (e.g., Roberts & Oosting 1958; Aldenius et al. -
Ancistrocladaceae
Soltis et al—American Journal of Botany 98(4):704-730. 2011. – Data Supplement S2 – page 1 Soltis, Douglas E., Stephen A. Smith, Nico Cellinese, Kenneth J. Wurdack, David C. Tank, Samuel F. Brockington, Nancy F. Refulio-Rodriguez, Jay B. Walker, Michael J. Moore, Barbara S. Carlsward, Charles D. Bell, Maribeth Latvis, Sunny Crawley, Chelsea Black, Diaga Diouf, Zhenxiang Xi, Catherine A. Rushworth, Matthew A. Gitzendanner, Kenneth J. Sytsma, Yin-Long Qiu, Khidir W. Hilu, Charles C. Davis, Michael J. Sanderson, Reed S. Beaman, Richard G. Olmstead, Walter S. Judd, Michael J. Donoghue, and Pamela S. Soltis. Angiosperm phylogeny: 17 genes, 640 taxa. American Journal of Botany 98(4): 704-730. Appendix S2. The maximum likelihood majority-rule consensus from the 17-gene analysis shown as a phylogram with mtDNA included for Polyosma. Names of the orders and families follow APG III (2009); other names follow Cantino et al. (2007). Numbers above branches are bootstrap percentages. 67 Acalypha Spathiostemon 100 Ricinus 97 100 Dalechampia Lasiocroton 100 100 Conceveiba Homalanthus 96 Hura Euphorbia 88 Pimelodendron 100 Trigonostemon Euphorbiaceae Codiaeum (incl. Peraceae) 100 Croton Hevea Manihot 10083 Moultonianthus Suregada 98 81 Tetrorchidium Omphalea 100 Endospermum Neoscortechinia 100 98 Pera Clutia Pogonophora 99 Cespedesia Sauvagesia 99 Luxemburgia Ochna Ochnaceae 100 100 53 Quiina Touroulia Medusagyne Caryocar Caryocaraceae 100 Chrysobalanus 100 Atuna Chrysobalananaceae 100 100 Licania Hirtella 100 Euphronia Euphroniaceae 100 Dichapetalum 100 -
Comparative Lm and Sem Studies of Glandular Trichomes on the Calyx of Flowers of Two Species of Plumbago Linn
Plant Archives Vol. 17 No. 2, 2017 pp. 948-954 ISSN 0972-5210 COMPARATIVE LM AND SEM STUDIES OF GLANDULAR TRICHOMES ON THE CALYX OF FLOWERS OF TWO SPECIES OF PLUMBAGO LINN. Smita S. Chaudhari and G. S.Chaudhari1 Department of Botany, Dr. A. G. D. Bendale Mahila Mahavidyalaya, Jalgaon (Maharashtra), India. 1P. G. Department of Botany, M. J. College, Jalgaon (Maharashtra), India. Abstract LM and SEM investigation of calyx of flowers of Plumbago zeylanica Linn. and Plumbago auriculata Lam. has shown two types of trichomes-glandular trichomes and unicellular trichomes. Basic structure of glandular trichomes in both taxa is same. Each trichome show multicellular stalk and head. The stalk penetrates the head. Heads of glandular trichomes in Plumbago zeylanica are colourless and translucent but in Plumbago auriculata colourless translucent as well as purple heads are noticed. In Plumbago zeylanica glandular trichomes have higher density, present throughout the length of calyx, distributed in random manner, oriented in different directions, show much more variation in lengths while in Plumbago auriculata glandular trichomes have lower density, present only in the upper part of calyx, arranged in linear fashion, tricomes in one line are oriented in the same direction, show less variation in lengths. EDAX analysis on the head of glandular trichomes of Plumbago zeylanica revealed only C, O, Mg, Al and Si but in Plumbago auriculata in addition to these elements Na, S, Cl, K, Ca, Ti, Fe were also found. Presence of glandular trichomes secreting mucilage (which is considered as adhesive trap for prey) supports the protocarnivorous nature of Plumbago. Key words : Plumbago zeylanica Linn., Plumbago auriculata Lam., glandular trichomes, LM, SEM. -
Phylogeny and Biogeography of the Carnivorous Plant Family Droseraceae with Representative Drosera Species From
F1000Research 2017, 6:1454 Last updated: 10 AUG 2021 RESEARCH ARTICLE Phylogeny and biogeography of the carnivorous plant family Droseraceae with representative Drosera species from Northeast India [version 1; peer review: 1 approved, 1 not approved] Devendra Kumar Biswal 1, Sureni Yanthan2, Ruchishree Konhar 1, Manish Debnath 1, Suman Kumaria 2, Pramod Tandon2,3 1Bioinformatics Centre, North-Eastern Hill University, Shillong, Meghalaya, 793022, India 2Department of Botany, North-Eastern Hill University, Shillong, Meghalaya, 793022, India 3Biotech Park, Jankipuram, Uttar Pradesh, 226001, India v1 First published: 14 Aug 2017, 6:1454 Open Peer Review https://doi.org/10.12688/f1000research.12049.1 Latest published: 14 Aug 2017, 6:1454 https://doi.org/10.12688/f1000research.12049.1 Reviewer Status Invited Reviewers Abstract Background: Botanical carnivory is spread across four major 1 2 angiosperm lineages and five orders: Poales, Caryophyllales, Oxalidales, Ericales and Lamiales. The carnivorous plant family version 1 Droseraceae is well known for its wide range of representatives in the 14 Aug 2017 report report temperate zone. Taxonomically, it is regarded as one of the most problematic and unresolved carnivorous plant families. In the present 1. Andreas Fleischmann, Ludwig-Maximilians- study, the phylogenetic position and biogeographic analysis of the genus Drosera is revisited by taking two species from the genus Universität München, Munich, Germany Drosera (D. burmanii and D. Peltata) found in Meghalaya (Northeast 2. Lingaraj Sahoo, Indian Institute of India). Methods: The purposes of this study were to investigate the Technology Guwahati (IIT Guwahati) , monophyly, reconstruct phylogenetic relationships and ancestral area Guwahati, India of the genus Drosera, and to infer its origin and dispersal using molecular markers from the whole ITS (18S, 28S, ITS1, ITS2) region Any reports and responses or comments on the and ribulose bisphosphate carboxylase (rbcL) sequences. -
Carnivorous Plants with Hybrid Trapping Strategies
CARNIVOROUS PLANTS WITH HYBRID TRAPPING STRATEGIES BARRY RICE • P.O. Box 72741 • Davis, CA 95617 • USA • [email protected] Keywords: carnivory: Darlingtonia californica, Drosophyllum lusitanicum, Nepenthes ampullaria, N. inermis, Sarracenia psittacina. Recently I wrote a general book on carnivorous plants, and while creating that work I spent a great deal of time pondering some of the bigger issues within the phenomenon of carnivory in plants. One of the basic decisions I had to make was select what plants to include in my book. Even at the genus level, it is not at all trivial to produce a definitive list of all the carnivorous plants. Seventeen plant genera are commonly accused of being carnivorous, but not everyone agrees on their dietary classifications—arguments about the status of Roridula can result in fistfights!1 Recent discoveries within the indisputably carnivorous genera are adding to this quandary. Nepenthes lowii might function to capture excrement from birds (Clarke 1997), and Nepenthes ampullaria might be at least partly vegetarian in using its clusters of ground pitchers to capture the dead vegetable mate- rial that rains onto the forest floor (Moran et al. 2003). There is also research that suggests that the primary function of Utricularia purpurea bladders may be unrelated to carnivory (Richards 2001). Could it be that not all Drosera, Nepenthes, Sarracenia, or Utricularia are carnivorous? Meanwhile, should we take a closer look at Stylidium, Dipsacus, and others? What, really, are the carnivorous plants? Part of this problem comes from the very foundation of how we think of carnivorous plants. When drafting introductory papers or book chapters, we usually frequently oversimplify the strategies that carnivorous plants use to capture prey. -
TREE November 2001.Qxd
Review TRENDS in Ecology & Evolution Vol.16 No.11 November 2001 623 Evolutionary ecology of carnivorous plants Aaron M. Ellison and Nicholas J. Gotelli After more than a century of being regarded as botanical oddities, carnivorous populations, elucidating how changes in fitness affect plants have emerged as model systems that are appropriate for addressing a population dynamics. As with other groups of plants, wide array of ecological and evolutionary questions. Now that reliable such as mangroves7 and alpine plants8 that exhibit molecular phylogenies are available for many carnivorous plants, they can be broad evolutionary convergence because of strong used to study convergences and divergences in ecophysiology and life-history selection in stressful habitats, detailed investigations strategies. Cost–benefit models and demographic analysis can provide insight of carnivorous plants at multiple biological scales can into the selective forces promoting carnivory. Important areas for future illustrate clearly the importance of ecological research include the assessment of the interaction between nutrient processes in determining evolutionary patterns. availability and drought tolerance among carnivorous plants, as well as measurements of spatial and temporal variability in microhabitat Phylogenetic diversity among carnivorous plants characteristics that might constrain plant growth and fitness. In addition to Phylogenetic relationships among carnivorous plants addressing evolutionary convergence, such studies must take into account have been obscured by reliance on morphological the evolutionary diversity of carnivorous plants and their wide variety of life characters1 that show a high degree of similarity and forms and habitats. Finally, carnivorous plants have suffered from historical evolutionary convergence among carnivorous taxa9 overcollection, and their habitats are vanishing rapidly. -
FILOGENIA E BIOGEOGRAFIA DE DROSERACEAE INFERIDAS a PARTIR DE CARACTERES MORFOLÓGICOS E MOLECULARES (18S, Atpb, Matk, Rbcl E ITS)
FILOGENIA E BIOGEOGRAFIA DE DROSERACEAE INFERIDAS A PARTIR DE CARACTERES MORFOLÓGICOS E MOLECULARES (18S, atpB, matK, rbcL e ITS) VITOR FERNANDES OLIVEIRA DE MIRANDA Tese apresentada ao Instituto de Biociências da Universidade Estadual Paulista “Julio de Mesquita Filho”, Campus de Rio Claro, para a obtenção do título de Doutor em Ciências Biológicas (Área de Concentração: Biologia Vegetal) Rio Claro Estado de São Paulo – Brasil Abril de 2.006 FILOGENIA E BIOGEOGRAFIA DE DROSERACEAE INFERIDAS A PARTIR DE CARACTERES MORFOLÓGICOS E MOLECULARES (18S, atpB, matK, rbcL e ITS) VITOR FERNANDES OLIVEIRA DE MIRANDA Orientador: Prof. Dr. ANTONIO FURLAN Co-orientador: Prof. Dr. MAURÍCIO BACCI JÚNIOR Tese apresentada ao Instituto de Biociências da Universidade Estadual Paulista “Julio de Mesquita Filho”, Campus de Rio Claro, para a obtenção do título de Doutor em Ciências Biológicas (Área de Concentração: Biologia Vegetal) Rio Claro Estado de São Paulo – Brasil Abril de 2.006 582 Miranda, Vitor Fernandes Oliveira de M672f Filogenia e biogeografia de Droseraceae inferidas a partir de caracteres morfológicos e moleculares (18S, atpB, matK, rbcL e ITS) / Vitor Fernandes Oliveira de Miranda. – Rio Claro : [s.n.], 2006 132 f. : il., figs., tabs., fots. Tese (doutorado) – Universidade Estadual Paulista, Institu- to de Biociências de Rio Claro Orientador: Antonio Furlan Co-orientador: Mauricio Bacci Junior 1. Botânica – Classificação. 2. Botânica sistemática molecu- lar. 3. Aldrovanda. 4. Dionaea. 5. Drosera. 6. DNA. I. Título. Ficha Catalográfica elaborada pela STATI – Biblioteca da UNESP Campus de Rio Claro/SP iv Agradecimentos Ao Prof. Furlan por sua sabedoria, por toda a sua paciência, por toda a sua compreensão, que sempre soube me ouvir e sempre me viu, acima de tudo, como pessoa. -
Droseraceae Gland and Germination Patterns Revisited: Support for Recent Molecular Phylogenetic Studies
DROSERACEAE GLAND AND GERMINATION PATTERNS REVISITED: SUPPORT FOR RECENT MOLECULAR PHYLOGENETIC STUDIES JOHN G. CONRAN • Centre for Evolutionary Biology and Biodiversity • Environmental Biology • School of Earth and Environmental Sciences • Darling Building DP418 • The University of Adelaide • SA 5005 • Australia • [email protected] GUNTA JAUDZEMS • Department of Ecology and Evolutionary Biology • Monash University • Clayton • Vic. 3168 • Australia NEIL D. HALLAM • Department of Ecology and Evolutionary Biology • Monash University • Clayton • Vic. 3168 • Australia Keywords: Physiology: Aldrovanda, Dionaea, Drosera. Abstract Droseraceae germination and leaf gland and microgland character state patterns were re-exam- ined in the light of new molecular phylogenetic relationships. Phanerocotylar germination is basal in the family, with cryptocotylar germination having evolved at least twice; once in Aldrovanda, and again in Drosera within the Bryastrum/Ergaleium clade. Gland patterns also support major clades; with the Bryastrum clade taxa having marginal and Rorella-type glands whereas the terminal branch of the Drosera clade had marginal glands and most of the clade possessed biseriate type 3 glands. The gland and germination patterns are supported by growth habit features, suggesting that the family and the main clades within Drosera in particular have undergone major adaptive radiations for these charac- ters. Introduction Relationships between the genera and species of Droseraceae have been the subject of numerous studies, with a range of morphology-based systems produced, mainly using traditional characters such as habit, leaf-associated features and specialised propagation techniques (e.g. Planchon 1848; Diels 1906). Character evolution of traps has also been considered important in carnivorous plants (Juniper et al. 1989; Jobson & Albert 2002) and glandular patterns (Seine & Barthlott 1992, 1993; Länger et al. -
Targeted Flora and Fauna Habitat Survey of Proposed Development
Targeted Flora and Fauna Habitat Survey of Proposed Development in Swan View Prepared for Statewest Planning Ref: T18022 Terratree Pty Ltd ABN 48 159 6065 005 Unit 3, No. 42 Victoria Street, Midland WA 6056 Telephone: (08) 9250 1163 Mobile: 0400 003 688 Email: [email protected] www.terratree.com.au Document Control Revision Details Date Author Reviewer Rev 0 Internal Review 10/01/2019 G. Maslen J. Grehan Rev A Draft for Submission to Client for Review 23/01/2019 G. Maslen J. Grehan Rev B Final Submission to Client 07/02/2019 G. Maslen S. O’Hara Joseph Grehan Director and Principal Ecologist Targeted Flora and Fauna Survey of Proposed Development in Swan View for Statewest Planning i DISCLAIMER This document is prepared in accordance with and subject to an agreement between Terratree Pty Ltd (“Terratree”) and the client for whom it has been prepared (“Statewest Planning”) and is restricted to those issues that have been raised by the client in its engagement of Terratree and prepared using the standard of skill and care ordinarily exercised by Environmental Scientists in the preparation of such documents. Any organisation or person that relies on or uses this document for purposes or reasons other than those agreed by Terratree and the client without first obtaining the prior written consent of Terratree, does so entirely at their own risk and Terratree denies all liability in tort, contract or otherwise for any loss, damage or injury of any kind whatsoever (whether in negligence or otherwise) that may be suffered as a consequence of relying on this document for any purpose other than that agreed with the client. -
Ovule and Seed Development in Droseraceae
Acta Bot. Need. 38(3), September 1989, p. 295-311 Ovule and seed development in Droseraceae F.D. Boesewinkel Hugo de Vries Laboratorium, University of Amsterdam, Kruislaan 318,1098 SM Amsterdam SUMMARY A structural analysis ofovule and seed development in the fourgenera of the Droseraceae is given. The ovule primordia ofthe Droseraceaeare dizonate. The dermalin The ovules of integuments are origin. Dionaea, Aldrovandaand Drosera are characterized by nucellarelongation and strongly enlarged cells of the nucellarepidermis. This featureis lacking in Drosophyllum. The differences in the seed coat ofthe four generaare mainly due to variationsin the differentiationof the testa. Drosophyllum has an endotestalcrystal layer, Dionaeaand Aldrovandaare exotestal andexo-/endotestal respectively, whereas Drosera has a less complex testa. Contrary to the testa, the tegmenshows more correspondence. It consists of an endotegmic sclerotized orpigment layer and crushed in of the variable remaining outer tegmic layers. As a consequence, spite basic similar testa structure the seed coat structure is in the four genera. In Drosophyllum, Dionaeaand Drosera the sclerotic layers ofthe seed coat are not lignified. Although the seed dimensionsare different, the operculate seeds with starchy endosperm and smallembryo have a similar construction. From the point ofview of the seed anatomy, the four genera are correctly placed in the Droseraceae. Key-words: Droseraceae, endotegmen, operculum, seed anatomy. INTRODUCTION The family Droseraceae consists of carnivorous