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Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
Introduction to Common Native & Invasive Freshwater Plants in Alaska
Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska Cover photographs by (top to bottom, left to right): Tara Chestnut/Hannah E. Anderson, Jamie Fenneman, Vanessa Morgan, Dana Visalli, Jamie Fenneman, Lynda K. Moore and Denny Lassuy. Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska This document is based on An Aquatic Plant Identification Manual for Washington’s Freshwater Plants, which was modified with permission from the Washington State Department of Ecology, by the Center for Lakes and Reservoirs at Portland State University for Alaska Department of Fish and Game US Fish & Wildlife Service - Coastal Program US Fish & Wildlife Service - Aquatic Invasive Species Program December 2009 TABLE OF CONTENTS TABLE OF CONTENTS Acknowledgments ............................................................................ x Introduction Overview ............................................................................. xvi How to Use This Manual .................................................... xvi Categories of Special Interest Imperiled, Rare and Uncommon Aquatic Species ..................... xx Indigenous Peoples Use of Aquatic Plants .............................. xxi Invasive Aquatic Plants Impacts ................................................................................. xxi Vectors ................................................................................. xxii Prevention Tips .................................................... xxii Early Detection and Reporting -
Effect of Different Water Temperatures on Growth of Aquatic Plants Salvinia Natans and Ceratophyllum Demersum
Journal of Coastal Life Medicine 2017; 5(1): 13-15 13 Journal of Coastal Life Medicine journal homepage: www.jclmm.com Original article https://doi.org/10.12980/jclm.5.2017J6-213 ©2017 by the Journal of Coastal Life Medicine. All rights reserved. Effect of different water temperatures on growth of aquatic plants Salvinia natans and Ceratophyllum demersum Khadija Kadhem Hreeb* Marine Biology Department, Marine Science Center, University of Basrah, Basrah, Iraq ARTICLE INFO ABSTRACT Article history: Objective: To evaluate the effect of some different water temperatures on growth of aquatic Received 8 Oct 2016 plants (Salvinia natans and Ceratophyllum demersum). Received in revised form 14 Nov 2016 Methods: The aquatic plants were brought from Shatt Al-Arab River in 2016. Equal weights of Accepted 2 Dec 2016 aquatic plants were aquacultured in aquaria, and were exposed to three different temperatures ( Available online 15 Dec 2016 12, 22 and 32 °C). Results: The results showed that the two plants did not show significant differences with respect to their effects on pH and electrical conductivity values. Time and temperature did not affect the values of pH and electrical conductivity. The values of dissolved oxygen was Keywords: significantly influenced with variation of time and temperature, while the two plants did not Temperatures have significant differences on dissolved oxygen values, nitrate ion concentration and was not Aquatic plants significantly influenced with variation of plant species or temperature or time. Plant species Shatt Al-Arab River and temperature significantly affected phosphate ion concentration, while the time did not Salvinia natans significantly influence the concentration of phosphate ion. -
A Key to Common Vermont Aquatic Plant Species
A Key to Common Vermont Aquatic Plant Species Lakes and Ponds Management and Protection Program Table of Contents Page 3 Introduction ........................................................................................................................................................................................................................ 4 How To Use This Guide ....................................................................................................................................................................................................... 5 Field Notes .......................................................................................................................................................................................................................... 6 Plant Key ............................................................................................................................................................................................................................. 7 Submersed Plants ...................................................................................................................................................................................... 8-20 Pipewort Eriocaulon aquaticum ...................................................................................................................................................................... 9 Wild Celery Vallisneria americana .................................................................................................................................................................. -
Internal Eutrophication: How It Works and What to Do About It – a Review
Chemistry and Ecology Vol. 22, No. 2, April 2006, 93–111 Internal eutrophication: How it works and what to do about it – a review A. J. P. SMOLDERS*, L. P. M. LAMERS, E. C. H. E. T. LUCASSEN, G. VAN DER VELDE and J. G. M. ROELOFS Department of Ecology, Institute for Water and Wetland Research, Radboud University Nijmegen, Toernooiveld 1, 6525 ED Nijmegen, The Netherlands (Received 18 November 2005; in final form 16 January 2006) In the 1980s and 1990s, it became increasingly clear that changes in external nutrient loads alone could not entirely explain the severe eutrophication of surface waters in the Netherlands. Nowadays, ‘internal eutrophication’ has become a widely accepted term in Dutch water management practice to describe the eutrophication of an ecosystem without additional external input of nutrients (N, P, K). This review surveys the principal mechanisms involved in this process. It also discusses possible remedies to combat internal eutrophication. Keywords: Alkalinity; Anaerobic decomposition; Biomanipulation; Internal eutrophication; Nitrate; Phosphate; Sulphate 1. Introduction In the Netherlands, the term internal eutrophication (‘interne eutrofiëring’ in Dutch) has become popular through publications by Roelofs and co-workers since the late 1980s [1–8]. Most of these publications were written in Dutch and described the eutrophication of surface waters in Dutch peaty lowlands as a result of changes in water quality without additional external supply of nutrients (N, P, K). Their ideas were based on the observation that water quality had deteriorated considerably, even in nature reserves, although in many cases no significant increase had occurred in the external nutrient loads [1, 3, 5]. -
Riparian Vegetation of the River Murray COVER: Healthy Red Gum in the Kex)Ndrook State Forest Near Barham N.S.W
Riparian Vegetation of The River Murray COVER: Healthy red gum in the Kex)ndrook State Forest near Barham N.S.W. Background, black box silhouette. PHOTO: D. Eastburn ISBN 1 R75209 02 6 RIVER MURRAY RIPARIAN VEGET ION STUDY PREPARED FOR: MURRAY-DARLING BASIN COMMISSION BY: MARGULES AND PARTNERS PTY LTD PAND J SMITH ECOLOGICAL CONSULTANTS DEPARTMENT OF CONSERVATION FORESTS AND LANDS VICTORIA January 1990 SUMMARY AND CONCLUSIONS The River Murray Riparian Vegetation Survey was initiated by the Murray Darling Basin Commission t9 assessJhe present status ofthe vegetationalong the Murray, to identify causes ofdegradation, and to develop solutions for its rehabilitation and long term stability. The study area was the floodplain of the Murray River and its anabranches, including the Edward-Wakool system, from below Hume Dam to the upper end of Lake Alexandrina. The components of the study were: · Literature Review A comprehensive bibliography was compiled on the floodplain vegeta tion, its environment and the impact ofman's activities. The literature was reviewed and summarised. · Floristic Survey A field survey was carried out, visiting 112 sites throughout the study area and collecting vegetation data from 335 plots. Data collected were the species present, their relative abundance, the condition of the eucalypts, the amount ofeucalypt regeneration and indices ofgrazing pressure. Brief studies were made of the effects of river regulation and salinisation at specific sites. Thirty-seven plant communities were identified from a numerical analyis ofthe floristic survey data. The differences reflect environmental changes both along the river and across the floodplain. The most important factors were identified as soil salinity levels and flooding frequency. -
Ancient Aquatic Angiosperms Flow from the Fossil Record Donald H
COMMENTARY COMMENTARY Water from the rock: Ancient aquatic angiosperms flow from the fossil record Donald H. Les1 the rapid rise of angiosperms has intrigued Department of Ecology and Evolutionary Biology, University of Connecticut, Storrs, CT 06269 paleoecologists and evolutionary biologists, who have strived to elucidate underlying ex- planations for their successful radiation. La- The world of 120 million years ago was one dominant global floristic element, a transfor- mented by Charles Darwin as “an abomina- of dynamic biological processes. During that mative event that ultimately altered the char- ble mystery” (1), the abrupt appearance of time the flowering plants emerged as the acter of the entire planet. Understandably, angiosperms and their sudden burst of diver- sification in the fossil record continues to captivate contemporary plant systematists, who have sought a solution by incorporating massive amounts of DNA sequence data in comparative phylogenetic studies of extant species. However, despite extensive techno- logical advances in genetics, genomics, and bioinformatics, which have revolutionized plant research over the past decades, our comprehension of life on earth during such ancient times continues to rely primarily on one data source: the fossil record. In PNAS, Gomez et al. (2) uncover an important clue to Darwin’s mystery by their analyses of Monteschia vidalii,anenigmaticplantfossil from Barremian deposits in Spain. Their re- interpretation of these fossils provides a new perspective that allies Monteschia not only with the angiosperms, but specifically with extant members of the order Ceratophyllales, a group of considerable interest in debates concerning the origin of flowering plants. The characterization of these early plants as highly specialized aquatics also offers novel interpretations regarding the ecological char- acteristics of early angiosperms. -
Different Reutilization of Mineral Nutrients in Senescent Leaves Of
Aquatic Botany 119 (2014) 1–6 Contents lists available at ScienceDirect Aquatic Botany jou rnal homepage: www.elsevier.com/locate/aquabot Different reutilization of mineral nutrients in senescent leaves of aquatic and terrestrial carnivorous Utricularia species ∗ Lubomír Adamec Institute of Botany of the Academy of Sciences of the Czech Republic, Section of Plant Ecology, Dukelská 135, CZ-379 82 Treboˇ n,ˇ Czech Republic a r t i c l e i n f o a b s t r a c t Article history: Nutrient reutilization (recycling) from senescent tissues in aquatic and terrestrial plants is important Received 24 February 2014 especially in nutrient-poor environments. The hypothesis was verified that N and P are reutilized effi- Received in revised form 2 June 2014 ciently from senescent shoots in both aquatic and terrestrial plants, while K is reutilized only in terrestrial Accepted 7 June 2014 plants. The efficiency of N, P and K reutilization in old traps and shoot segments in the submerged carnivo- Available online 16 June 2014 rous plant Utricularia reflexa and the leaves of non-carnivorous Ceratophyllum submersum was compared with that in the leaves of five terrestrial Utricularia species. Oxygen-based dark respiration rates of U. Keywords: reflexa traps, measured as a criterion of physiological activity, exhibited a marked polarity, while a weak Lentibulariaceae respiration polarity of leaves was not significant. No distinct polarity of trap and shoot N contents were Aquatic and terrestrial plants found in U. reflexa shoots. When the correction factor of 0.71 was applied to compensate for the assumed Aerobic dark respiration Shoot polarity dry weight (DW) decrease in old traps and leaf nodes, the mean reutilization efficiency for N was 19% in Senescence traps and 37% in leaf nodes and for P, 67% in traps and 52% in leaf nodes. -
Zooplankton Diversity and Macrophyte Biometry in Shallow Water Bodies of Various Trophic State
Hydrobiologia (2016) 774:39–51 DOI 10.1007/s10750-015-2595-4 WETLANDS BIODIVERSITY AND PROCESSES Zooplankton diversity and macrophyte biometry in shallow water bodies of various trophic state Natalia Kuczyn´ska-Kippen . Tomasz Joniak Received: 18 September 2015 / Revised: 12 November 2015 / Accepted: 17 November 2015 / Published online: 1 December 2015 Ó The Author(s) 2015. This article is published with open access at Springerlink.com Abstract In order to determine whether using indi- elimination of macrophyte-dominated refuges, cators of zooplankton diversity and macrophyte thereby lowering the macrophyte-site share, which parameters (density and biomass) could be a useful ranged from 47% in eutrophy, 40% in mesotrophy to tool for diagnosing the water quality of ponds we only 20% in hypereutrophy. Therefore, we assume that hypothesised that in various trophic types of shallow zooplankton diversity and macrophyte occurrence can water bodies parameters of a macrophyte habitat will be used for quality assessment of small water bodies. reflect zooplankton diversity. Thus, 439 stations (open water, helophytes, elodeids) were studied among 274 Keywords Shallow ponds Á Rotifer and crustacean pastoral ponds (mid-west Poland). In each trophic diversity Á Trophic status Á Aquatic plant biomass Á state of waters a key predictor of zooplankton diversity Environmental predictors was biomass of macrophytes attributed to a variety of ecological types or various species of macrophytes. A shift from the high importance of elodeids (e.g. Myriophyllum, Ceratophyllum demersum) in structur- Introduction ing zooplankton diversity in mesotrophic waters to helophytes (Typha angustifolia, Phragmites australis, Ponds, which are considered to be small ecological Schoenoplectus lacustris) in hypereutrophic ponds complexes, form model systems for studying various was recorded. -
Relationships of Submerged Aquatic Vegetation of Mississippi Coastal River Systems
2010 Mississippi Water Resources Conference Relationships of submerged aquatic vegetation of Mississippi Coastal river systems James A. Garner, Jackson Stat University Hyun J. Cho, Jackson State University Patrick Biber, University of Southern Mississippi Submerged aquatic vegetation (SAV) provide many valuable environmental functions. Unfortunately, their abundance has declined globally and their location within the watershed has shifted due to landscape alterations. The purpose of this study is to develop habitat indices that can be widely used to predict SAV type and their distribution in varying locations and habitat or basin types. SAV communities of shallow waters in channels, adjoining bayous, streams, inlets, and lagoons of the Pascagoula River, Back Bay of Biloxi, and Pearl River systems of coastal Mississippi were surveyed from May 2008 to June 2010. The survey extended upstream to where stream width became narrow and shade from tall trees on the shore restricted SAV growth. The location and species of SAV and the nearby floating aquatic and dominant shoreline emergent plants were recorded. The locations were added onto base GIS (Geographic Information System) maps for determination of landscape parameters. Locations were partitioned by presence or absence of each of four important SAV species for comparison of the following landscape features: distance to the Mississippi Sound, width of water course, and frequency of occurrence of other SAV and shore vegetation species. Analysis of SAV occurrence in the Mississippi coastal river systems indicates that a substantial number of plant associations exist. Plant-site associations were not fully explained by salinity tolerance alone, and may be influenced by multiple inherent traits of the individual species. -
A Synopsis of Zannichellia L. (Potamogetonaceae) in Iran
IRANIAN JOURNAL OF BOTANY 25 (2), 2019 DOI: 10.22092/ijb.2019.128488.1263 A SYNOPSIS OF ZANNICHELLIA L. (POTAMOGETONACEAE) IN IRAN Sh. Abbasi, S. Afsharzadeh & M. Dinarvand Received 2019. 11. 20; accepted for publication 2019. 12. 10 Abbasi, Sh., Afsharzadeh, S. & Dinarvand, M. 2019. 12. 30: A synopsis of Zannichellia L. (Potamogetonaceae) in Iran. -Iran. J. Bot. 25 (2): 103-114. Tehran. Zannichellia L. (Potamogetonaceae) is a cosmopolitan genus widely distributed in aquatic ecosystems of Iran. The last taxonomic treatment of this genus dates back to 1971 in Flora Iranica, with some recent modifications in Flora of Iran. This research aimed to provide a new taxonomic treatment of Zannichellia in Iran based on distributional, morphological, and molecular studies (using ITS, PHYB, trnH-psbA and rpl32-trnL molecular markers). In this research, one species (Zannichellia palustris) with two varieties is distinguished. An identification key to varieties is presented and descriptions of them are provided. A distribution map of the genus in Iran is compiled. The distribution is concentrated in northern, central and southwestern parts of Iran. Shabnam Abbasi, Saeed Afsharzadeh (correspondence <[email protected]>), Department of Plant and Animal Biology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran. -Mehri Dinarvand, Forests and Rangelands Research Division, Khuzestan Agricultural and Natural Resources Research and Education Center, Ahvaz, Agricultural Research Education and Extension Organization (AREEO), -
First Record of Potamogetonaceae for the State of Rio Grande Do Norte
http://dx.doi.org/10.1590/1519-6984.06814 Notes and Comments First record of Potamogetonaceae for the state of Rio Grande do Norte, Brazil Henry-Silva, GG.a*, Moura, RST.a, Lopes, YVA.a and Rodrigues, RS.b aUniversidade Federal Rural do Semi-Árido – UFERSA, Campus Mossoró, Avenida Francisco Mota, 572, Costa e Silva, CEP 59625-900, Mossoró, RN, Brazil bCentro de Estudos da Biodiversidade, Universidade Federal de Roraima – UFRR, Av. Cap. Ene Garcez 2413, Aeroporto, CEP 69310-000, Boa Vista, RR, Brazil *e-mail: [email protected] Received: April 25, 2014 – Accepted: May 9, 2014 – Distributed: December 31, 2014 Potamogetonaceae is a small subcosmopolitan monocot early cosmopolitan and is represented in the Neotropics family of aquatic herbs with submersed or floating leaves, only by P. pusillus var. pusillus, where it extends from belonging to the order Alismatales (Haynes and Holm-Nielsen, Mexico to Argentina (Haynes and Holm-Nielsen, 2003). It 2003). It is a taxonomically complex family (Kaplan et al., has been recorded for some states in all Brazilian regions, 2013), which may comprise three or more genera, depending with the exception of the northern region (Bove, 2014a). on the including of Zannichelliaceae (Haynes and Holm- In the Northeastern region, P. pusillus has been found in Nielsen, 2003; APGIII 2009; Kaplan et al., 2013). the states of Alagoas, Bahia, Ceará, Paraíba, Pernambuco Potamogeton is the largest genus of Potamogetonaceae, (Bove, 2014a, b). with ca. of 72 species (Kaplan et al., 2013), occurring mainly The record of P. pusillus in the Santa Cruz reservoir in temperate regions (Haynes and Holm-Nielsen, 2003).