Special Status Species Study
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
The Vascular Plants of Massachusetts
The Vascular Plants of Massachusetts: The Vascular Plants of Massachusetts: A County Checklist • First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Somers Bruce Sorrie and Paul Connolly, Bryan Cullina, Melissa Dow Revision • First A County Checklist Plants of Massachusetts: Vascular The A County Checklist First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Massachusetts Natural Heritage & Endangered Species Program Massachusetts Division of Fisheries and Wildlife Natural Heritage & Endangered Species Program The Natural Heritage & Endangered Species Program (NHESP), part of the Massachusetts Division of Fisheries and Wildlife, is one of the programs forming the Natural Heritage network. NHESP is responsible for the conservation and protection of hundreds of species that are not hunted, fished, trapped, or commercially harvested in the state. The Program's highest priority is protecting the 176 species of vertebrate and invertebrate animals and 259 species of native plants that are officially listed as Endangered, Threatened or of Special Concern in Massachusetts. Endangered species conservation in Massachusetts depends on you! A major source of funding for the protection of rare and endangered species comes from voluntary donations on state income tax forms. Contributions go to the Natural Heritage & Endangered Species Fund, which provides a portion of the operating budget for the Natural Heritage & Endangered Species Program. NHESP protects rare species through biological inventory, -
No Evidence for a Large Atmospheric CO2 Spike Across the Cretaceous
RESEARCH LETTER No Evidence for a Large Atmospheric CO2 Spike Across 10.1029/2018GL081215 the Cretaceous‐Paleogene Boundary Key Points: Joseph N. Milligan1,2 , Dana L. Royer1 , Peter J. Franks3 , Garland R. Upchurch4 , • Understanding atmospheric CO 2 1 across the Cretaceous‐Paleogene and Melissa L. McKee boundary has been limited due to 1 2 deficiencies in existing records Department of Earth and Environmental Sciences, Wesleyan University, Middletown, CT, USA, Department of Geology, • Our study highlights the utility of a Baylor University, Waco, TX, USA, 3School of Life and Environmental Sciences, University of Sydney, Sydney, New South proxy based on leaf gas exchange Wales, Australia, 4Department of Biology, Texas State University, San Marcos, TX, USA principles • We record a small transient rise in atmospheric CO2 that is more in line ‐ fi with modeled estimates of both Abstract Currently, there is only one paleo CO2 record from plant macrofossils that has suf cient Deccan volcanism and a bolide stratigraphic resolution to potentially capture a transient spike related to rapid carbon release at the impact Cretaceous‐Paleogene (K‐Pg) boundary. Unfortunately, the associated measurements of stomatal index are off‐calibration, leading to a qualitative interpretation of >2,300‐ppm CO2. Here we reevaluate this record Supporting Information: ‐ • Supporting Information S1 with a paleo CO2 proxy based on leaf gas exchange principles. We also test the proxy with three living species • Data Set S1 grown at 500‐ and 1,000‐ppm CO2, including the nearest living relative of the K‐Pg fern, and find a mean error rate of ~22%, which is comparable to other leading paleo‐CO2 proxies. -
Vascular Flora of the Possum Walk Trail at the Infinity Science Center, Hancock County, Mississippi
The University of Southern Mississippi The Aquila Digital Community Honors Theses Honors College Spring 5-2016 Vascular Flora of the Possum Walk Trail at the Infinity Science Center, Hancock County, Mississippi Hanna M. Miller University of Southern Mississippi Follow this and additional works at: https://aquila.usm.edu/honors_theses Part of the Biodiversity Commons, and the Botany Commons Recommended Citation Miller, Hanna M., "Vascular Flora of the Possum Walk Trail at the Infinity Science Center, Hancock County, Mississippi" (2016). Honors Theses. 389. https://aquila.usm.edu/honors_theses/389 This Honors College Thesis is brought to you for free and open access by the Honors College at The Aquila Digital Community. It has been accepted for inclusion in Honors Theses by an authorized administrator of The Aquila Digital Community. For more information, please contact [email protected]. The University of Southern Mississippi Vascular Flora of the Possum Walk Trail at the Infinity Science Center, Hancock County, Mississippi by Hanna Miller A Thesis Submitted to the Honors College of The University of Southern Mississippi in Partial Fulfillment of the Requirement for the Degree of Bachelor of Science in the Department of Biological Sciences May 2016 ii Approved by _________________________________ Mac H. Alford, Ph.D., Thesis Adviser Professor of Biological Sciences _________________________________ Shiao Y. Wang, Ph.D., Chair Department of Biological Sciences _________________________________ Ellen Weinauer, Ph.D., Dean Honors College iii Abstract The North American Coastal Plain contains some of the highest plant diversity in the temperate world. However, most of the region has remained unstudied, resulting in a lack of knowledge about the unique plant communities present there. -
Hybrids in the Fern Genus Osmunda (Osmundaceae)
Bull. Natl. Mus. Nat. Sci., Ser. B, 35(2), pp. 63–69, June 22, 2009 Hybrids in the Fern Genus Osmunda (Osmundaceae) Masahiro Kato Department of Botany, National Museum of Nature and Science, Amakubo 4–1–1, Tsukuba, 305–0005 Japan E-mail address: [email protected] Abstract Four described putative hybrids in genus Osmunda, O. intermedia from Japan, O. rug- gii from eastern U.S.A., O. nipponica from central Japan, and O. mildei from southern China, are enumerated with notes on their hybridity. It is suggested that Osmunda intermedia is an intrasub- generic hybrid (O. japonica of subgenus Osmunda ϫ O. lancea of subgenus Osmunda), O. ruggii is an intersubgeneric hybrid (O. regalis of subgenus Osmunda ϫ O. claytoniana of subgenus Clay- tosmunda), O. nipponica is an intersubgeneric hybrid (O. japonica ϫ O. claytoniana of subgenus Claytosmunda), and O. midlei is an intersubgeneric hybrid (O. japonica ϫ O. angustifolia or O. vachellii of subgenus Plenasium). Among the four, O. intermedia is the most widely distributed and can reproduce in culture, suggesting that it can reproduce to some extent in nature. Key words : Hybrid, Osmunda intermedia, Osmunda mildei, Osmunda nipponica, Osmunda rug- gii. three subgenera Claytosmunda, Osmunda, and Introduction Plenasium, genus Leptopteris, genus Todea, and The genus Osmunda has been classified in ei- genus Osmundastrum (see also Metzgar et al., ther the broad or narrow sense. In the previously 2008). most accepted and the most lumping classifica- Four putative hybrids are known in the genus tion, it was divided into three subgenera, Osmun- Osmunda s.l. in eastern U.S.A. -
Wool-Grass – Mannagrass Mixed Shrub Marsh
Wool-grass – Mannagrass Mixed Shrub Marsh System: Palustrine Subsystem: Herbaceous PA Ecological Group(s): Vernal Pool Global Rank: GNR State Rank: S4 General Description The Wool-grass – mannagrass mixed shrub marsh pool occurs in seasonally to somewhat permanently inundated depressions throughout Pennsylvania. The type can be described as a seasonally flooded, herbaceous swamp with well defined boundaries; some pools of this type exhibit somewhat poorly defined boundaries. The surrounding plant community varies with region, soils, and geology. The pools are generally deeper than those of the Rice cutgrass – bulrush marsh pool and may not dry completely over the summer months. This community is characterized as an open, seasonally to permanently flooded depression, dominated by herbaceous and shrubby species; wool-grass (Scirpus cyperinus) is usually dominant. Common co- dominant and associate species include floating mannagrass (Glyceria septentrionalis), rattlesnake mannagrass (Glyceria canadensis), rice cutgrass (Leersia oryzoides), pale meadowgrass (Torreyochloa pallida), sedges (e.g. Carex crinita, C. lurida, C. lupulina, C. vesicaria, C. folliculata), three-way sedge (Dulichium arundinaceum), mild water-pepper (Persicaria hydropiperoides), marsh-purslane (Ludwigia palustris), marsh St. Johns-wort (Triadenum fraseri). The federally endangered species, northeastern bulrush (Scirpus ancistrochaetus), is also found in this type. Shrubs include hardhack (Spiraea tomentosa), meadow-sweet (S. alba), northern arrow-wood (Viburnum recognitum), highbush blueberry (Vaccinium corymbosum), and buttonbush (Cephalanthus occidentalis). Canopy trees, which are limited to the pool margins, most often include white oak (Quercus alba), sourgum (Nyssa sylvatica), and red maple (Acer rubrum). Rank Justification Uncommon but not rare; some cause for long-term concern due to declines or other factors. Identification Open, seasonally flooded depression, dominated by herbaceous plants, usually graminoids. -
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. -
Conserving Plant Diversity in New England
CONSERVING PLANT DIVERSITY IN NEW ENGLAND A COLLABORATION OF CONSERVING PLANT DIVERSITY IN NEW ENGLAND A COLLABORATION OF AUTHORS Mark Anderson Director of Conservation Science, Eastern United States, The Nature Conservancy Michael Piantedosi Director of Conservation, Native Plant Trust William Brumback Director of Conservation Emeritus, Native Plant Trust MAP PRODUCTION Arlene Olivero WEB TOOL Melissa Clark DESIGN Rachel Wolff-Lander Kate Wollensak Freeborn The authors wish to thank the six state Natural Heritage programs for sharing their data and for their support. ©2021 Published June 2021 © Peter James CONTENTS EXECUTIVE SUMMARY ES-1 PART ONE: CONSERVING PLANT DIVERSITY 1-1 Background 1-2 • Plant Diversity and Resilience 1-2 • Global Strategy for Plant Conservation and Global Deal for Nature 1-7 • Secured Lands and GAP Status 1-9 • New England Flora and Rare Taxa 1-11 • Threats to Plant Diversity in New England 1-14 • Conservation Actions to Counter Threats to Plant Diversity 1-17 Conservation of Habitats and Important Plant Areas 1-21 Introduction 1-21 • Terminology 1-21 • Overview and Methods 1-22 Conservation of Habitats: Progress Toward Global and Regional Goals 1-26 • Matrix Forests 1-26 • Wetlands 1-30 • Patch-forming Habitats 1-33 • Risk of Conversion 1-36 Conservation of Important Plant Areas (IPAs) 1-37 • Definition and Location of IPAs 1-37 • Conservation Status and Progress Toward Goals 1-40 • Representation of Habitats in the IPAs 1-42 Conservation of Threatened Species 1-48 • Threatened Plants Conserved in situ 1-48 • Threatened Plants Conserved in ex situ Collections 1-49 Results and Recommendations 1-58 i CONTENTS continued PART TWO: STATUS REPORT AND MAPS 2-1 Overview 2-4 New England’s Terrestrial Habitats 2-7 Map Page Layout 2-13 Upland Habitats: Matrix Forest 2-16 Upland Habitats: Patch-forming Habitats 2-53 Wetland Habitats 2-80 PART THREE: SUPPORTING MATERIAL 3-1 Bibliography 3-2 Appendices 3-11 1. -
Bomfleur Et Al. (2017): the Fossil Osmundales
Bomfleur et al. (2017): The fossil Osmundales (Royal Ferns)—a phylogenetic network analysis, revised taxonomy, and evolutionary classification of anatomically preserved trunks and rhizomes. this study l) a rm fo n /i s ) u e ly n b i e s ri ) m y g u t e fa il b n b ib b u e u r u am (S G (S (T S F Wang et al. (2014)* Osmunda s) s) u l) l) u n a a n e s m y m s e g u r il r u g b n fo fo n b u e n am n e u (S G (i F (i G (S Tidwell & Ash (1994) s) s) Plenasium Plenasium u ly y u n i il n e s m y m s e g a l a g a Claytosmunda b u f i f u b a b b n d u n m e u d S e u a u S n ( G S F S G ( n u u m m s s O O nae p p Osmunda u u Osmunda o o ndi r r g g n n Osmunda Osmunda smu w w O o o r r c c a a Osmundastrum ndeae d d Osmundastrum Osmundastrum n n u u O. (Claytosmunda) O. (Claytosmunda) smu O m m s Osmundastrum s Osmundastrum O O Todea Todea Plenasium ) m l Leptopteris Leptopteris u a Plenasium Plenasium i s Miller (1971) rm a fo n e in l s/ P y u il n y m s e Todea Todea il fa u g b n b m u e u Fa S (S Millerocaulis Millerocaulis Aurealcaulis G Leptopteris Leptopteris Osmunda Millerocaulis Millerocaulis e e Todea a a e e c c nae a a a d d d n n n odei u T u u Leptopteris m m m s Osmundastrum s s O O O Plenasium Osmundoideae Millerocaulis group e a e d i o p p d e e Todea u u n e e a a o o u a a r r Ashicaulis e e Ashicaulis e e e Ashicaulis g g Ashicaulis m c c a d d s i i a a e m m O o o Leptopteris e e d d c d d t t n n n n a s s u u u u d m m n m m s s u s s O O m O O s O s s i i l herbstii group l u u a a c c a o r d e l n l Ashicaulis -
VH Flora Complete Rev 18-19
Flora of Vinalhaven Island, Maine Macrolichens, Liverworts, Mosses and Vascular Plants Javier Peñalosa Version 1.4 Spring 2019 1. General introduction ------------------------------------------------------------------------1.1 2. The Setting: Landscape, Geology, Soils and Climate ----------------------------------2.1 3. Vegetation of Vinalhaven Vegetation: classification or description? --------------------------------------------------3.1 The trees and shrubs --------------------------------------------------------------------------3.1 The Forest --------------------------------------------------------------------------------------3.3 Upland spruce-fir forest -----------------------------------------------------------------3.3 Deciduous woodlands -------------------------------------------------------------------3.6 Pitch pine woodland ---------------------------------------------------------------------3.6 The shore ---------------------------------------------------------------------------------------3.7 Rocky headlands and beaches ----------------------------------------------------------3.7 Salt marshes -------------------------------------------------------------------------------3.8 Shrub-dominated shoreline communities --------------------------------------------3.10 Freshwater wetlands -------------------------------------------------------------------------3.11 Streams -----------------------------------------------------------------------------------3.11 Ponds -------------------------------------------------------------------------------------3.11 -
Rice Cutgrass – Bulrush Vernal Pool
Rice Cutgrass – Bulrush Vernal Pool System: Palustrine Subsystem: Herbaceous PA Ecological Group(s): Vernal Pool Global Rank: GNR, G1 State Rank: S2? General Description This community is characterized as an open, seasonally flooded, mixed-herbaceous wetland meadow with defined basin boundaries and usually occurs within dry, oak-dominated forests with open canopies. Common dominant species include pale meadowgrass (Torreyochloa pallida), mannagrass (Glyceria acutiflora), rattlesnake mannagrass (Glyceria canadensis), three-way sedge (Dulichium arundinaceum), Canada bluejoint (Calamagrostis canadensis), rice cutgrass (Leersia oryzoides), sedges (e.g. Carex tribuloides, C. lurida, C. gynandra, C. vesicaria, C. folliculata), dotted smartweed (Persicaria punctata), marsh St. Johns-wort (Triadenum fraseri), royal fern (Osmunda regalis), needle spike-rush (Eleocharis acicularis), and white beak-rush (Rhynchospora alba). The federally endangered species, northeastern bulrush (Scirpus ancistrochaetus), is also found in this type, and can sometimes comprise a significant area within the pool. The invasive low smartweed (Persicaria longiseta) was present within this type in some pools and stiltgrass (Microstegium vimineum), can form dense patches on the edges of the pools. Shrubs such as winterberry (Ilex verticillata) and swamp dewberry (Rubus hispidus) are present, but never dominant and canopy trees most often include white oak (Quercus alba), sourgum (Nyssa sylvatica), and red maple (Acer rubrum). The pools may also contain a substantial bryophyte -
Fern Classification
16 Fern classification ALAN R. SMITH, KATHLEEN M. PRYER, ERIC SCHUETTPELZ, PETRA KORALL, HARALD SCHNEIDER, AND PAUL G. WOLF 16.1 Introduction and historical summary / Over the past 70 years, many fern classifications, nearly all based on morphology, most explicitly or implicitly phylogenetic, have been proposed. The most complete and commonly used classifications, some intended primar• ily as herbarium (filing) schemes, are summarized in Table 16.1, and include: Christensen (1938), Copeland (1947), Holttum (1947, 1949), Nayar (1970), Bierhorst (1971), Crabbe et al. (1975), Pichi Sermolli (1977), Ching (1978), Tryon and Tryon (1982), Kramer (in Kubitzki, 1990), Hennipman (1996), and Stevenson and Loconte (1996). Other classifications or trees implying relationships, some with a regional focus, include Bower (1926), Ching (1940), Dickason (1946), Wagner (1969), Tagawa and Iwatsuki (1972), Holttum (1973), and Mickel (1974). Tryon (1952) and Pichi Sermolli (1973) reviewed and reproduced many of these and still earlier classifica• tions, and Pichi Sermolli (1970, 1981, 1982, 1986) also summarized information on family names of ferns. Smith (1996) provided a summary and discussion of recent classifications. With the advent of cladistic methods and molecular sequencing techniques, there has been an increased interest in classifications reflecting evolutionary relationships. Phylogenetic studies robustly support a basal dichotomy within vascular plants, separating the lycophytes (less than 1 % of extant vascular plants) from the euphyllophytes (Figure 16.l; Raubeson and Jansen, 1992, Kenrick and Crane, 1997; Pryer et al., 2001a, 2004a, 2004b; Qiu et al., 2006). Living euphyl• lophytes, in turn, comprise two major clades: spermatophytes (seed plants), which are in excess of 260 000 species (Thorne, 2002; Scotland and Wortley, Biology and Evolution of Ferns and Lycopliytes, ed. -
The Paraphyly of Osmunda Is Confirmed by Phylogenetic Analyses of Seven Plastid Loci
Systematic Botany (2008), 33(1): pp. 31–36 © Copyright 2008 by the American Society of Plant Taxonomists The Paraphyly of Osmunda is Confirmed by Phylogenetic Analyses of Seven Plastid Loci Jordan S. Metzgar,1 Judith E. Skog,2,3 Elizabeth A. Zimmer,4 and Kathleen M. Pryer1,5 1Department of Biology, Duke University, Durham, North Carolina 27708 U.S.A. 2Department of Environmental Science and Policy, George Mason University, Fairfax, Virginia 22030 U.S.A. 3National Science Foundation, Division of Biological Infrastructure, 4201 Wilson Blvd., Arlington, Virginia 22203 U.S.A. 4Department of Botany and Laboratory of Analytical Biology, Smithsonian Museum Support Center, 4210 Silver Hill Road, Suitland, Maryland 20746 U.S.A. 5Author for correspondence ([email protected]) Communicating Editor: Daniel Potter Abstract—To resolve phylogenetic relationships among all genera and subgenera in Osmundaceae, we analyzed over 8,500 characters of DNA sequence data from seven plastid loci (atpA, rbcL, rbcL–accD, rbcL–atpB, rps4–trnS, trnG–trnR, and trnL–trnF). Our results confirm those from earlier anatomical and single-gene (rbcL) studies that suggested Osmunda s.l. is paraphyletic. Osmunda cinnamomea is sister to the remainder of Osmundaceae (Leptopteris, Todea, and Osmunda s.s.). We support the recognition of a monotypic fourth genus, Osmundastrum, to reflect these results. We also resolve subgeneric relationships within Osmunda s.s. and find that subg. Claytosmunda is strongly supported as sister to the rest of Osmunda. A stable, well-supported classification for extant Osmundaceae is proposed, along with a key to all genera and subgenera. Keywords—ferns, Osmunda, Osmundaceae, Osmundastrum, paraphyly, plastid DNA.