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Buy new guinea impatiens, impatiens hawkeri (any color) - plant online at nurserylive | Best plants at lowest price New Guinea Impatiens, Impatiens Hawkeri (Any Color) - Plant New Guinea impatiens Rating: Not Rated Yet Price Variant price modifier: Base price with tax Price with discount ?399 Salesprice with discount Sales price ?399 Sales price without tax ?399 Discount Tax amount Ask a question about this product Description Impatiens hawkeri is a species of flowering plant in the family Balsaminaceae. It is native to Papua New Guinea and the Solomon Islands. It has been bred and hybridized in cultivation to produce a line of garden plants. Common name: New Guinea impatiens Color: Pink,purple Bloom time: Flowers freely Height: 1.50 to 4.00 feet Difficulty level: easy to grow Planting & Care Plant impatiens transplants after the last spring frost in humus-rich, moist, well-drained soil. Make sure the plants have some shelter from the wind. You can mix in compost or a slow-release fertilizer before transplanting to help the plants. Sunlight: Part shade Soil: well-drained soil Water: Medium Temprature: 74 to 77°F Fertilizer: Apply any organic fertilizer Care: The most important thing to remember about impatiens plants is to water them regularly. Keep them moist, but not too wet. 1 / 2 Buy new guinea impatiens, impatiens hawkeri (any color) - plant online at nurserylive | Best plants at lowest price If the plants dry out, they will lose their leaves. If you over-water the plants, this could encourage fungal diseases. Remember container plants will need more water. Special Feature: Mass or group in beds and borders. Tall ground cover. Edging along walks or paths. Containers, window boxes and hanging baskets. Houseplant. Use Medicinal use: The plant is harvested from the wild for local medicinal use Ornamental use: The plant is used for ornamental purpose. Note: No serious insect or disease problems. Reference: http://www.almanac.com/plant/impatiens Reviews Monday, 20 January 2020 is the pot and soil included? Purvi Sangani Thursday, 28 November 2019 Awesome experience!!! Luved the plant. Looked exactly the same. Thank you NL Dheeraj Yadav Saturday, 23 November 2019 How often I need to water it? Sunaina Raj More reviews 2 / 2 Powered by TCPDF (www.tcpdf.org).

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(Balsaminaceae) Using Chloroplast Atpb-Rbcl Spacer Sequences
Systematic Botany (2006), 31(1): pp. 171–180 ᭧ Copyright 2006 by the American Society of Plant Taxonomists Phylogenetics of Impatiens and Hydrocera (Balsaminaceae) Using Chloroplast atpB-rbcL Spacer Sequences STEVEN JANSSENS,1,4 KOEN GEUTEN,1 YONG-MING YUAN,2 YI SONG,2 PHILIPPE KU¨ PFER,2 and ERIK SMETS1,3 1Laboratory of Plant Systematics, Institute of Botany and Microbiology, Kasteelpark Arenberg 31, B-3001 Leuven, Belgium; 2Institut de Botanique, Universite´ de Neuchaˆtel, Neuchaˆtel, Switzerland; 3Nationaal Herbarium Nederland, Universiteit Leiden Branch, PO Box 9514, 2300 RA Leiden, The Netherlands 4Author for correspondence ([email protected]) ABSTRACT. Balsaminaceae are a morphologically diverse family with ca. 1,000 representatives that are mainly distributed in the Old World tropics and subtropics. To understand the relationships of its members, we obtained chloroplast atpB-rbcL sequences from 86 species of Balsaminaceae and five outgroups. Phylogenetic reconstructions using parsimony and Bayesian approaches provide a well-resolved phylogeny in which the sister group relationship between Impatiens and Hydrocera is confirmed. The overall topology of Impatiens is strongly supported and is geographically structured. Impatiens likely origi- nated in South China from which it colonized the adjacent regions and afterwards dispersed into North America, Africa, India, the Southeast Asian peninsula, and the Himalayan region. Balsaminaceae are annual or perennial herbs with in the intrageneric relationships of Impatiens. The most flowers that exhibit a remarkable diversity. The family recent molecular intrageneric study on Balsaminaceae consists of more than 1,000 species (Grey-Wilson utilized Internal Transcribed Spacer (ITS) sequences 1980a; Clifton 2000), but only two genera are recog- and provided new phylogenetic insights in Impatiens nized.
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(19) United States (12) Plant Patent Application Publication (10) Pub
US 200701133 12A1 (19) United States (12) Plant Patent Application Publication (10) Pub. No.: US 2007/0113312 P1 Kawashima (43) Pub. Date: May 17, 2007 (54) NEW GUINEA IMPATIENS PLANT NAMED Publication Classification MSATO FG3 (51) Int. Cl. (76) Inventor: Moriya Kawashima, Nagano-ken (JP) AOIH 5/00 (2006.01) (52) U.S. Cl. ............................................................ PLT/318 Correspondence Address: JONDLE & ASSOCATES P.C. 858 HAPPY CANYON ROAD SUTE 230 (57) ABSTRACT CASTLE ROCK, CO 80108 (US) (21) Appl. No.: 11/272,989 A New Guinea Impatiens cultivar particularly distinguished by its high blooming temperature and large magenta flowers (22) Filed: Nov. 14, 2005 is disclosed. GENUS AND SPECIES including blooms, buds, and foliage of the plant; the colors shown are as true as can be reasonably obtained by conven 0001 Impatiens interspecific cross Impatiensxhybrida tional photographic procedures. VARIETY DENOMINATION 0012 FIG. 1. The photograph shows overall plant habit 0002 Misato FG3 including blooms, buds and foliage. 0013 FIG. 2. The photograph shows the mature inflo BACKGROUND OF THE NEW PLANT CSCCC. 0003. The present invention comprises a new and distinct cultivar of New Guinea impatiens, botanically known as DETAILED DESCRIPTION OF THE NEW Impatiensxhybrida, and hereinafter referred to by the culti CULTIVAR var name Misato FG3. Misato FG3 originated from an 0014) The following detailed descriptions set forth the interspecific hybridization between 2K-MC-1, an unpat distinctive characteristics of Misato FG3. The data which ented orange-flowered Impatiens hawkeri plant and 8B-4C define these characteristics were collected from asexual 1, an unpatented proprietary red-flowered Impatiens platy reproductions carried out in Salinas, Calif.
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Phylogenetic Utility of the AP3/DEF K-Domain and Its Molecular Evolution in Impatiens (Balsaminaceae)
Molecular Phylogenetics and Evolution 43 (2007) 225–239 www.elsevier.com/locate/ympev Phylogenetic utility of the AP3/DEF K-domain and its molecular evolution in Impatiens (Balsaminaceae) Steven Janssens a,*, Koen Geuten a, Tom Viaene a, Yong-Ming Yuan b, Yi Song b, Erik Smets a,c a Laboratory of Plant Systematics, Institute of Botany and Microbiology, Kasteelpark Arenberg 31, BE-3001 Leuven, Belgium b Institut de Botanique, Universite´ de Neuchaˆtel, Neuchaˆtel, Switzerland c National Herbarium of the Netherlands, Leiden University Branch, PO Box 9514, NL-2300 RA Leiden, The Netherlands Received 24 March 2006; revised 15 November 2006; accepted 16 November 2006 Available online 26 November 2006 Abstract APETALA3 (AP3)/DEFICIENS (DEF) is a MADS-box transcription factor that is involved in establishing the identity of petal and stamen floral organs. The AP3/DEF gene lineage has been extensively examined throughout the angiosperms in order to better under- stand its role in floral diversity and evolution. As a result, a large number of cloned AP3/DEF orthologues are available, which can be used for the design of taxon specific primers for phylogeny reconstruction of close relatives of the group of interest. Following this reasoning, we investigated the phylogenetic utility of the two AP3/DEF paralogues (ImpDEF1 and ImpDEF2) that were recently iden- tified in the genus Impatiens (Balsaminaceae). K-domain introns 4 and 5 of both AP3/DEF duplicates were amplified and sequenced for 59 Impatiens species. Phylogenetic analyses of the separated and combined ImpDEF1 and ImpDEF2 data sets result in highly congruent topologies with the previously obtained chloroplast atpB-rbcL data set.
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Pollinator Attractors: Petaloidy and Petal Epidermal Cell Shape in Close Relatives of Snapdragon
Pollinator attractors: petaloidy and petal epidermal cell shape in close relatives of snapdragon By Copyright 2011 Jacob Brian Landis Submitted to the graduate degree program in Ecology and Evolutionary Biology and the Graduate Faculty of the University of Kansas in partial fulfillment of the requirements for the degree of Master of Arts. ________________________________ Chairperson Dr. Lena Hileman ________________________________ Dr. Mark Mort ________________________________ Dr. Paulyn Cartwright Date Defended: April 13, 2011 ii The Thesis Committee for Jacob B Landis certifies that this is the approved version of the following thesis: Pollinator attractors: petaloidy and petal epidermal cell shape in close relatives of snapdragon ________________________________ Chairperson Dr. Lena Hileman Date approved: 30 June 2011 1 ABSTRACT The diversity of angiosperms in floral form and development has been an area of interest for biologists. A multitude of studies investigating the evolution of flowering plants have attempted to determine why angiosperms are so diverse. One possible major contributor to flower form diversity is pollinator pressure. The interactions between flowers and their pollinators have important ecological and evolutionary consequences, with co-evolution often occuring. Many studies have looked at suites of floral traits that affect pollinator visitation, which have been coined pollination syndromes (Fenster et al., 2004). These traits include but are not limited to, flower color, flower orientation, landing platforms, and nectar guides. With the increase in genetic tools, and the utilization of model species such as Antirrhinum majus(Plantaginaceae) and Arabidopsis thaliana (Brassicaeae), many studies are looking at the geneitc architecture of floral traits. Studies have determined the genetic blueprint for floral oragn identity, as well as in traits asociated with pollination syndromes including flower color and symmetry.
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Evolution of Petaloid Sepals Independent of Shifts in B-Class MADS Box Gene Expression
Landis et al 1 1 Evolution of petaloid sepals independent of shifts in B-class MADS box gene expression 2 3 Jacob B. Landis1,2, Laryssa L. Barnett3 and Lena C. Hileman 4 5 Department of Ecology and Evolutionary Biology, University of Kansas, 1200 Sunnyside Avenue, Lawrence, KS 6 66045, USA 7 8 1Author for correspondence email: [email protected], phone: 352-273-2977, fax: 352-392-3704 9 10 2Present Address: Department of Biology, University of Florida, Gainesville, Florida 32608 11 3Present Address: Department of Biology, Duke University, Durham, North Carolina 27708 12 13 14 15 16 17 18 19 20 21 22 23 Landis et al 2 24 ABSTRACT 25 Attractive petals are an integral component of animal-pollinated flowers, and in many flowering plant species are 26 restricted to the second floral whorl. Interestingly, multiple times during angiosperm evolution, petaloid 27 characteristics have expanded to adjacent floral whorls or to extra-floral organs. Here we investigate developmental 28 characteristics of petaloid sepals in Rhodochiton atrosanguineum, a close relative of the model species Antirrhinum 29 majus (snapdragon). We undertook this in two ways, first using scanning electron microscopy (SEM) we investigate 30 micromorphology of petals and sepals, followed by expression studies of genes usually responsible for the formation 31 of petaloid structures. From our data, we conclude that R. atrosanguineum petaloid sepals lack micromorphological 32 characteristics of petals, and that petaloid sepals did not evolve through regulatory evolution of B-class MADS box 33 genes, which have been shown to specify second whorl petal identity in a number of model flowering plant species 34 including snapdragon.
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Evolution of the Interaction of Floral Homeotic Proteins
Evolution of the interaction of floral homeotic proteins Dissertation Zur Erlangung des akademischen Grades ‘doctor rerum naturalium‘ (Dr. rer. nat.) Vorgelegt dem Rat der Biologisch-Pharmazeutischen Fakultät der Friedrich-Schiller-Universität Jena von Diplombiologe Florian Rümpler geboren am 04. Dezember 1986 in Erfurt Gutachter 1. Prof. Dr. Günter Theißen (Jena) 2. Asst. Prof. Dr. Rainer Melzer (Dublin) 3. Prof. Dr. Richard Immink (Wageningen) Tag der öffentlichen Verteidigung Mittwoch 15. November 2017 Table of contents 1 Introduction ............................................................................................................................... 3 1.1 MADS-domain transcription factors in plants - a K-domain blessing .............................. 3 1.2 MIKCC-type MADS-TFs controlling flower development of angiosperms ..................... 6 1.3 The protein-protein interaction network of floral homeotic proteins ................................ 8 1.4 The keratin-like domain of MIKCC-type proteins ............................................................. 9 1.5 Floral homeotic proteins as targets of plant pathogen effectors ...................................... 11 1.6 Aims of this thesis ........................................................................................................... 14 2 Manuscripts ............................................................................................................................. 15 2.1 Manuscript overview ......................................................................................................
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An Ecological Assessment of Impatiens Glandulifera in Its Introduced and Native Range and the Potential for Its Classical Biological Control
An Ecological Assessment of Impatiens glandulifera in its Introduced and Native range and the Potential for its Classical Biological Control By Robert A. Tanner Thesis submitted for the degree of Doctor of Philosophy School of Biological Sciences Royal Holloway, University of London October 2011 1 Declaration of Authorship I, Robert Tanner, hereby declare that the research, experimental design and data analysis for this thesis was conducted by myself with the exception of the following: • Sonal Varia (CABI) identified the 2007 ground Vortis samples presented in chapter 2 under my supervision and assisted in the 2008 sampling at Harmondsworth Moor. • Alex Lee (Royal Holloway) conducted the experiment of plant performance in different soil types, under my supervision for chapter 4. • Liang Jin (Royal Holloway) conducted the evaluation of the colonisation of arbuscular mycorrhizal fungi for the UK and Indian plants for chapter 5. • Richard Weaver (Royal Holloway) assisted in collecting the Carabid samples for chapter 3. Robert Tanner Professor Alan Gange 2 Abstract The diversity of vegetation, the above and below-ground invertebrate community, and the soil mycobiota are intrinsically linked. However, few studies have assessed the impact of non-native invasive plant species at all levels. Here, dynamics of vegetation complexity, the invertebrate community, and abundance of arbuscular mycorrhizae (AM) were evaluated in relation to the abundance of Impatiens glandulifera. The abundance of above-ground detritivores, herbivores, and predators was significantly lower in the invaded sites compared to the uninvaded sites. The below- ground community showed significant fluctuations within and between years, however, the overall abundance of the below-ground community showed no significant difference.
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Identification of Invasive Alien Species Using DNA Barcodes
Identification of Invasive Alien Species using DNA barcodes Royal Belgian Institute of Natural Sciences Royal Museum for Central Africa Rue Vautier 29, Leuvensesteenweg 13, 1000 Brussels , Belgium 3080 Tervuren, Belgium +32 (0)2 627 41 23 +32 (0)2 769 58 54 General introduction to this factsheet The Barcoding Facility for Organisms and Tissues of Policy Concern (BopCo) aims at developing an expertise forum to facilitate the identification of biological samples of policy concern in Belgium and Europe. The project represents part of the Belgian federal contribution to the European Research Infrastructure Consortium LifeWatch. Non-native species which are being introduced into Europe, whether by accident or deliberately, can be of policy concern since some of them can reproduce and disperse rapidly in a new territory, establish viable populations and even outcompete native species. As a consequence of their presence, natural and managed ecosystems can be disrupted, crops and livestock affected, and vector-borne diseases or parasites might be introduced, impacting human health and socio-economic activities. Non-native species causing such adverse effects are called Invasive Alien Species (IAS). In order to protect native biodiversity and ecosystems, and to mitigate the potential impact on human health and socio-economic activities, the issue of IAS is tackled in Europe by EU Regulation 1143/2014 of the European Parliament and Council. The IAS Regulation provides for a set of measures to be taken across all member states. The list of Invasive Alien Species of Union Concern is regularly updated. In order to implement the proposed actions, however, methods for accurate species identification are required when suspicious biological material is encountered.
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The Canadian Botanical Association Bulletin Bulletin de l'Association Botanique du Canada Fall colours at the Queen’s University Biological Station on Lake Opinicon, ©Greg Bulte. See article on page 63 Highlights in this issue: Major Invasive Plants: Fall Colours Top Ornamental Plants: Eurasian Water Milfoil Impatiens page 63 page 52 page 67 IN THIS ISSUE: President’s Message 36 2017 CBA Conference 37 2016/17 CBA Board of Directors and Section Chairs 38 Announcements 40 Teaching Section News 41 Mycology Section News 41 Reﬂections on CBA-ABC 2016, Victoria BC 42 2016 CBA Awards 45 Regional Award Winners recognized by CBA-ABC in 2016 49 Laurie Consaul Northern Research Scholarship Report: My journey to the North 51 Major Invasive Alien Plants of Natural Habitats in Canada 52 The Annual Show of Tree Leaf Colour 63 Top Canadian Ornamental Plants. 14. Impatiens 67 Diane Davis, CBA President Art Davis, and Christine Maxwell ©Hugues Massicotte 34 49(2) CBA/ABC Bulletin CBA members Olivera Gavric, Jarnail Chandi, Jason Wong, and Santokh Singh, celebrating “Fascination of Plants Day”, May 18, 2016 at UBC. Host your own event in 2017 - for more details see fascinationofplantsday.org The Canadian Botanical Association Bulletin Bulletin de l’Association Botanique du Canada The CBA Bulletin is issued three times a year (March, Septem- Le Bulletin de I’ABC paraît trois fois par année, normalement en ber and December) and is freely available on the CBA website. mars, septembre et décembre. Il est envoyé à tous les membres Hardcopy subscriptions are available for a fee. de I’ABC.
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A Rapid Biodiversity Assessment of Papua New Guinea's Hindenburg Wall Region
A Rapid Biodiversity Assessment of Papua New Guinea’s Hindenburg Wall Region edited by Stephen Richards & Nathan Whitmore Published by: Wildlife Conservation Society Papua New Guinea Program PO BOX 277, Goroka, Eastern Highlands Province PAPUA NEW GUINEA Tel: +675-532-3494 www.wcs.org Editors: Stephen J. Richards and Nathan Whitmore. Authors: Leeanne E. Alonso, Ken P. Aplin, Arison Arihafa, Kyle N. Armstrong, Michael Hammer, Jiri Hulcr, John Par Kagl, Bensolo Ken, , John S. Lamaris, Andrea Lucky, Chris J. Müller, Stephen J. Richards, Eli Sarnat, Günther Theischinger, Fanie Venter, Nathan Whitmore, and Iain Woxvold. The Wildlife Conservation Society is a private, not-for-profit organisation exempt from federal income tax under section 501c(3) of the Inland Revenue Code. The opinions expressed in this publication are those of the contributors and do not necessarily reflect those of the Wildlife Conservation Society or PNG Sustainable Development Program. Suggested citation: Richards, S.J. and N. Whitmore (editors) 2015. A rapid biodiversity assessment of Papua New Guinea's Hindenburg Wall region. Wildlife Conservation Society Papua New Guinea Program. Goroka, PNG. ISBN: 978-0-9943203-0-8 Front cover Image: Rocky Roe (waterfall on approach to Minni Camp) Rear cover Image: Stephen J. Richards (Nyctimystes oktediensis) ©2015 Wildlife Conservation Society TABLE OF CONTENTS Acknowledgements ii Partner Organisation Profiles iii Participants & Authors v Executive Summary vii Introduction 1 Chapter 1: Traditional & Local Ecological Knowledge 3 Chapter 2: Vascular Plants 14 Chapter 3: Ants & Scolytine Beetles 44 Chapter 4: Butterflies 60 Chapter 5: Odonata (Dragonflies & Damselflies) 75 Chapter 6: Freshwater fishes 84 Chapter 7: Herpetofauna 94 Chapter 8: Birds 103 Chapter 9: Non-Flying Mammals 131 Chapter 10: Bats 161 i ACKNOWLEDGEMENTS Many people and organisations helped to facilitate the 2013 Hindenburg Wall survey.
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Origin and Evolution of Petals in Angiosperms
Plant Ecology and Evolution 146 (1): 5–25, 2013 http://dx.doi.org/10.5091/plecevo.2013.738 REVIEW Origin and evolution of petals in angiosperms Louis P. Ronse De Craene1,* & Samuel F. Brockington2 1Royal Botanic Garden Edinburgh20A Inverleith Row, Edinburgh, EH3 5LR, United Kingdom 2Department of Plant Sciences, University of Cambridge, Cambridge, CB2 3EA, United Kingdom *Author for correspondence: [email protected] Background and aims – The term ‘petal’ is loosely applied to a variety of showy non-homologous structures, generally situated in the second whorl of a differentiated perianth. Petaloid organs are extremely diverse throughout angiosperms with repeated derivations of petals, either by differentiation of a perianth, or derived from staminodes. The field of evo-devo has prompted re-analysis of concepts of homology and analogy amongst petals. Here the progress and challenges in understanding the nature of petals are reviewed in light of an influx of new data from phylogenetics, morphology and molecular genetics. Method and results – The complex web of homology concepts and criteria is discussed in connection to the petals, and terminology is subsequently defined. The variation and evolution of the perianth is then reviewed for the major clades of angiosperms. From this pan-angiosperm variation, we highlight and discuss several recurrent themes that complicate our ability to discern the evolution of the petal. In particular we emphasise the importance of developmental constraint, environmental stimuli, interrelationship between organs and cyclic patterns of loss and secondary gain of organs, and the development of a hypanthium or corona. Conclusions – A flexible approach to understanding ‘petals’ is proposed requiring consideration of the origin of the floral organ (stamen-derived or tepal-derived, or other), the functional role (sepaloid or petaloid organs), evolutionary history of the organismal lineage, and consideration of developmental forces acting on the whole flower.
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University of Florida Thesis Or Dissertation Formatting
EVOLUTION AND DEVELOPMENT OF PETALS IN AIZOACEAE (CARYOPHYLLALES) By SAMUEL FRASER BROCKINGTON A DISSERTATION PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA 2009 1 © 2009 Samuel Fraser Brockington 2 To my ma and pa 3 ACKNOWLEDGMENTS I acknowledge the assistance of numerous people and organizations that have contributed to this doctoral work. First and foremost, I thank my advisors Douglas and Pamela Soltis for their patient support and example. I thank Walter S. Judd for inspiring my interest in the evolution of angiosperms and for his insight into various aspects of this project. I thank David Oppenheimer and Paris Gray for their expertise and use of their in-situ facilities. I thank Elena M. Kramer for her advice and expertise at various stages of this project. The morphological development work would not have been possible without the help of Paula J Rudall at the Royal Botanic Gardens, Kew and Michael Frohlich at the Natural History Museum, London. I thank my supervisory committee for taking the time to read this dissertation. I thank Mark Whitten for taking so many superb photos and sharing his photographic equipment. Kurt Neubig kindly shared equipment. I thank my two undergraduate helpers Alexandre Roolse and Jeremy Ramdial for putting in some long hours and collecting substantial amounts of data. The research was funded by an Assembling the Tree of Life grant EF-0431266 (NSF) to D. E. Soltis and P. S. Soltis, Floral Genome Project NSF grant PGR-0115684 to D.
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