List of Rare, Threatened, and Endangered Species of Dorchester County
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1501:18-1-03 Endangered and Threatened Species
ACTION: Revised DATE: 10/22/2014 11:54 AM 1501:18-1-03 Endangered and threatened species. (A) The following species of plants are designated as endangered in Ohio. (1) Acer pensylvanicum L., Striped maple. (2) Aconitum noveboracense A. Gray, Northern monkshood. (3) Aconitum uncinatum L., Southern monkshood. (4) Agalinis auriculata (Michx.) Blake, Ear-leaved-foxglove. (5) Agalinis purpurea (L.) Pennell var. parviflora (Benth.) Boivin, Small purple-foxglove. (6) Agalinis skinneriana (Wood) Britt., Skinner's-foxglove. (7) Ageratina aromatica (L.) Spach, Small white snakeroot. (8) Agrostis elliottiana Schultes, Elliott's bent grass. (9) Amelanchier humilis Wiegand, Low serviceberry. (10) Amelanchier interior E.L. Nielsen, Inland serviceberry. (9)(11) Andropogon glomeratus (Walter) Britton, Bushy broom-sedge. (10)(12) Androsace occidentalis Pursh, Western rock-jasmine. (11)(13) Anomobryum filiforme (Dicks.) Solms, Common silver moss. (12)(14) Anomodon viticulosus (Hedw.) Hook. & Taylor, Long tail moss. (13)(15) Arabidopsis lyrata (Linnaeus) O’Kane & Al-Shehbaz, Lyre-leaved rock cress. (14)(16) Arabis patens Sullivant, Spreading rock cress. (15)(17) Arctostaphylos uva-ursi (L.) Spreng., Bearberry. (16)(18) Aralia hispida Vent., Bristly sarsaparilla. [ stylesheet: rule.xsl 2.14, authoring tool: i4i 2.0 ras3 May 23, 2014 10:53, (dv: 0, p: 120697, pa: 243620, ra: 421552, d: print date: 10/22/2014 08:00 PM 1501:18-1-03 2 (17)(19) Arethusa bulbosa L., Dragon's-mouth. (20) Aristida basiramea Engelm. ex Vasey, Forked Three-awn grass. (18)(21) Aristida necopina Shinners, False arrow-feather. (19)(22) Aronia arbutifolia (L.) Pers., Red chokeberry. (20)(23) Asplenium bradleyi D. C. Eaton, Bradley's spleenwort. -
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Ohio Administrative Code Rule 1501:18-1-03 Endangered and threatened species. Effective: January 30, 2021 (A) The following species of plants are designated as endangered in Ohio. (1) Acer pensylvanicum L., Striped maple. (2) Aconitum noveboracense A. Gray, Northern monkshood. (3) Aconitum uncinatum L., Southern monkshood. (4) Adlumia fungosa (Ait.) Greene, Allegheny-vine. (5) Agalinis auriculata (Michx.) Blake, Ear-leaved-foxglove. (6) Agalinis purpurea (L.) Pennell var. parviflora (Benth.) Boivin, Small purple-foxglove. (7) Agalinis skinneriana (Wood) Britt., Skinner's-foxglove. (8) Ageratina aromatica (L.) Spach, Small white snakeroot. (9) Agrostis elliottiana Schultes, Elliott's bent grass. (10) Amelanchier humilis Wiegand, Low serviceberry. (11) Amelanchier interior E.L. Nielsen, Inland serviceberry. (12) Amphidium mougeotii (Bruch, Schimper and W. Gmbel) Schimper, Mougeot's ice moss. (13) Andropogon glomeratus (Walter) Britton, Bushy broom-sedge. Page 1 (14) Androsace occidentalis Pursh, Western rock-jasmine. (15) Anomobryum filiforme (Dicks.) Solms, Common silver moss. (16) Anomodon viticulosus (Hedw.) Hook. and Taylor, Long tail moss. (17) Arabidopsis lyrata (L.) OKane and Al-Shehbaz, Lyre-leaved rock cress. (18) Arabis patens Sullivant, Spreading rock cress. (19) Arctostaphylos uva-ursi (L.) Spreng., Bearberry. (20) Aralia hispida Vent., Bristly sarsaparilla. (21) Arethusa bulbosa L., Dragon's-mouth. (22) Aristida basiramea Engelm. ex Vasey, Forked three-awn grass. (23) Aristida necopina Shinners, False arrow-feather. (24) Aronia arbutifolia (L.) Pers., Red chokeberry. (25) Asplenium bradleyi D.C. Eaton, Bradley's spleenwort. (26) Asplenium resiliens Kunze, Black-stemmed spleenwort. (27) Astragalus neglectus (T. and G.) Sheld., Cooper's milk-vetch. (28) Baptisia australis (L.) R. Br., Blue false indigo. (29) Barbula indica (Hooker) Sprengel in E.G. -
Aquatic Vascular Plant Species Distribution Maps
Appendix 11.5.1: Aquatic Vascular Plant Species Distribution Maps These distribution maps are for 116 aquatic vascular macrophyte species (Table 1). Aquatic designation follows habitat descriptions in Haines and Vining (1998), and includes submergent, floating and some emergent species. See Appendix 11.4 for list of species. Also included in Appendix 11.4 is the number of HUC-10 watersheds from which each taxon has been recorded, and the county-level distributions. Data are from nine sources, as compiled in the MABP database (plus a few additional records derived from ancilliary information contained in reports from two fisheries surveys in the Upper St. John basin organized by The Nature Conservancy). With the exception of the University of Maine herbarium records, most locations represent point samples (coordinates were provided in data sources or derived by MABP from site descriptions in data sources). The herbarium data are identified only to township. In the species distribution maps, town-level records are indicated by center-points (centroids). Figure 1 on this page shows as polygons the towns where taxon records are identified only at the town level. Data Sources: MABP ID MABP DataSet Name Provider 7 Rare taxa from MNAP lake plant surveys D. Cameron, MNAP 8 Lake plant surveys D. Cameron, MNAP 35 Acadia National Park plant survey C. Greene et al. 63 Lake plant surveys A. Dieffenbacher-Krall 71 Natural Heritage Database (rare plants) MNAP 91 University of Maine herbarium database C. Campbell 183 Natural Heritage Database (delisted species) MNAP 194 Rapid bioassessment surveys D. Cameron, MNAP 207 Invasive aquatic plant records MDEP Maps are in alphabetical order by species name. -
2003 Survey of Tributaries for Eurasian Watermilfoil
It\OARRIN \f!I fresh Water Institute , ;ammw 7 7 mmnrr I In 1lllIiI@i liD' mpw I't W1I$UU II1I1 =pw Lake George, New York Adirondack Field Station at Bolton Landing A SURVEY OF TRIBUTARIICS TO LAKE GEORGI':, NEW YORK FOR THE PRESENCE OF I:URASIAN WATERMILFOIL prepared lor The fund for Lake George hy Lawrence W, Eichler Research Scientist T,aurie Ahrens-Franklin Sr. Laboratory Technician & Charles W. Boylen Associate Director DaHin Fresh Water Institute Rensselaer "PolJ1echnic instItutt; Troy, NY 12180-3590 Bolton Lanchng, NY 12814 March 2004 DrWI Technical Report 20U4-4 TABLE OF CONTt<:NTS The Survey of Lake George Tributaries for Eurasian watermilfoil· 200J executive Summary III Inlroduction Methods Results and Discussioll 3 References 12 Acknowl edgcrncnls 13 Appendix A. Site Locations Appendix B. MacroJlhyte Community Assessmrut data 11 EXECUTIVE SUMMARY A survey of tributary Jellas in the south hasin of Lake George was conducted in 2003 to assess the extent of Eurasian watermi[foil (Myriophyllum spicatum L) infestation. The Darrin fresh Water blStitutc conducted the project with financial support from the fund for Lake George. Similar surveys were completed in 1987, 1989, 1991, 1994, 11)1)7 and 2000 as reference points. Delta areas were chosen as read; Iy identifiable points that historically harbor diverse assemblages of native aquatic plants. Results orthese surveys can he used to approximate the rate of spread of11111foil through the Lake George hasin. in 1987, when surveys were initiated, 30 percent of the sites were found to have milfoil. By 1989, this percentage had dropped to 23 percent due to harvesting of mil foil, although three new locations were found in 19R9. -
National List of Vascular Plant Species That Occur in Wetlands 1996
National List of Vascular Plant Species that Occur in Wetlands: 1996 National Summary Indicator by Region and Subregion Scientific Name/ North North Central South Inter- National Subregion Northeast Southeast Central Plains Plains Plains Southwest mountain Northwest California Alaska Caribbean Hawaii Indicator Range Abies amabilis (Dougl. ex Loud.) Dougl. ex Forbes FACU FACU UPL UPL,FACU Abies balsamea (L.) P. Mill. FAC FACW FAC,FACW Abies concolor (Gord. & Glend.) Lindl. ex Hildebr. NI NI NI NI NI UPL UPL Abies fraseri (Pursh) Poir. FACU FACU FACU Abies grandis (Dougl. ex D. Don) Lindl. FACU-* NI FACU-* Abies lasiocarpa (Hook.) Nutt. NI NI FACU+ FACU- FACU FAC UPL UPL,FAC Abies magnifica A. Murr. NI UPL NI FACU UPL,FACU Abildgaardia ovata (Burm. f.) Kral FACW+ FAC+ FAC+,FACW+ Abutilon theophrasti Medik. UPL FACU- FACU- UPL UPL UPL UPL UPL NI NI UPL,FACU- Acacia choriophylla Benth. FAC* FAC* Acacia farnesiana (L.) Willd. FACU NI NI* NI NI FACU Acacia greggii Gray UPL UPL FACU FACU UPL,FACU Acacia macracantha Humb. & Bonpl. ex Willd. NI FAC FAC Acacia minuta ssp. minuta (M.E. Jones) Beauchamp FACU FACU Acaena exigua Gray OBL OBL Acalypha bisetosa Bertol. ex Spreng. FACW FACW Acalypha virginica L. FACU- FACU- FAC- FACU- FACU- FACU* FACU-,FAC- Acalypha virginica var. rhomboidea (Raf.) Cooperrider FACU- FAC- FACU FACU- FACU- FACU* FACU-,FAC- Acanthocereus tetragonus (L.) Humm. FAC* NI NI FAC* Acanthomintha ilicifolia (Gray) Gray FAC* FAC* Acanthus ebracteatus Vahl OBL OBL Acer circinatum Pursh FAC- FAC NI FAC-,FAC Acer glabrum Torr. FAC FAC FAC FACU FACU* FAC FACU FACU*,FAC Acer grandidentatum Nutt. -
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Natural Barrens and Post Oak Flatwoods in Posey and Spencer Counties, Indiana James R. Aldrich and Michael A. Homoya Indiana Natural Heritage Program, Indiana Department of Natural Resources Indianapolis, Indiana 46204 Introduction Post oak flatwoods are xeric forested communities that are dominated by Quercus stellata with a relatively open canopy that allows a great deal of dispersed light to reach the forest floor. This forested community lacks the typical shrub-layer found in more mesic forested communities and appears "savanna-like". Characteristically, post oak flatwoods in Indiana are found on poorly drained nearly level soils of alluvial lacustrine terraces of the Ohio River and other major streams in the unglaciated region of the Wabash Lowland Physiographic Province (12). The understory is dominated by sedges and the content of organic matter in the soil appears to be very low. The barrens described herein are relatively small natural openings surrounded by post oak flatwoods where a fragipan is at or very near the surface. The vegetation in these bar- rens is not dominated by prairie grasses and forbs, but is closely related to the vegeta- tion of sandstone glades described for Illinois (21) and Missouri (18). Contemporary southern "flatwoods" of the Illinois Tillplain dominated by sweetgum {Liquidambar styraciflua), beech (Fagus grandifolia) and red maple (Acer rubrum) in southwestern Ohio (4) and southeastern Indiana have been described in detail (9,13,15,17). Indiana "barrens" dominated by prairie forbs and grasses (7) have been discovered recently and discussed (3,10). Flatwoods dominated by post oak have received limited attention in Illinois (16) where they have been referred to as "southern flatwoods" (21) and very little has been written about the Indiana post oak flatwoods. -
The Genera of Elatinaceae in the Southeastern United States Gordon C
Eastern Illinois University The Keep Faculty Research & Creative Activity Biological Sciences January 1986 The genera of Elatinaceae in the southeastern United States Gordon C. Tucker Eastern Illinois University, [email protected] Follow this and additional works at: http://thekeep.eiu.edu/bio_fac Part of the Biology Commons Recommended Citation Tucker, Gordon C., "The eg nera of Elatinaceae in the southeastern United States" (1986). Faculty Research & Creative Activity. 184. http://thekeep.eiu.edu/bio_fac/184 This Article is brought to you for free and open access by the Biological Sciences at The Keep. It has been accepted for inclusion in Faculty Research & Creative Activity by an authorized administrator of The Keep. For more information, please contact [email protected]. TUCKER, ELATINACEAE THE GENERA OF ELATINACEAE IN THE SOUTHEASTERN UNITED STATES 1 Gordon C. Tucker 2 ELATINACEAE Dumortier, Anal. Fam. PL 44, 49. 1829, "Elatinideae," (Waterwort Family) Annual or perennial plants (up to 50 cm tall) of aquatic or moist terrestrial habitats. Roots fibrous; lower nodes usually with adventitious roots. Plants glabrous or glandular pubescent throughout, with unicellular or multicellular multiseriate capitate trichomes. Leaves opposite or decussate, entire or coarsely serrate; stomata anomocytic; 3 stipules scarious. Flowers small, actinomorphic, lablished in the first p.. (Inn, nold >,h V »n \h 19S8) and continued < •> Carolina, Georgia, \ he area covered by the nei ic i lora in< hides North and South Mississippi, Arkansas, and Louisiana. The descriptions are based prim; , Alabama, 1 for Hi. oppo.tunities provided by the Generic Flor; I thanl., Norton Miller and Carroll Wood icr. Thomas . s help in the development c,1 ihepres. -
AQUATIC PLANTS – Seasonal Cycles Roberta Hill
AQUATIC PLANTS – Seasonal cycles Roberta Hill Life, whether we are aware of it or not, is dominated by cycles. The water cycle, the nutrient cycle, the cycle of life itself, are all natural processes, fundamental to life on earth, which essentially follow circular trajectories. One of the great joys of exploring the littoral zone is the discovery of the many ways in which nature’s cycles, grand and minute, elaborate and simple, are played out in these sun-filled watery places. The annual cycle of the seasons is one of the most obvious--and most extraordinary-- cyclical processes in the littoral zone. In Maine, where the environmental conditions vary so sharply from one season to the next, changes in these areas are especially dramatic and at no time are these conditions so extreme as in the winter. How do aquatic plant communities respond to the shortened days, the decrease in the intensity of the sun’s energy, the plummeting air and water temperatures, the transformation of the habitat from one that is warm and liquid, to one that encrusted under a thick layer of ice and snow? Though each species has its own unique approach to preparing for and surviving through the hardships of winter, there are some common strategies employed. Since most aquatic plants evolved from terrestrial plants, it is not surprising that many of their over-wintering strategies are similar to those of their wild and cultivated upland kin; strategies you may Cattails in winter already know well from observing the plants in your garden. Aquatic plants, just like garden plants, can be sorted into groups based up what they do in response to winter and how they provide for regeneration the following spring. -
Fire in the Southeastern Grasslands, By
Fire in the Southeastern Grasslands RICHARD J. VOGL Department of Biology California State University Los Angeles, CA 90032 INTRODUCTION ~ERE has been more research on the effects of fire in the southeastern United States than in any region of North America. Most studies have been concerned with the effects of fire on the trees, including the role of fire in controlling hardwood suc cession, fire damage to trees, the effects of fire on soils and litter, the influence of fire on conifer growth and reproduction, and the relationships of fire to tree diseases (Garren 1943; Ahlgren and Ahlgren 1960; Cushwa 1968). A lesser, but stilI substantial number of studies have been focused on the effects of fire on forage yields and livestock production (Wahlenberg et al. 1939), and the use of fire in wildlife management in the Southeast. But academic or phy tosociological studies of the vegetational composition and of the effects of fire on the understory vegetation are generally lacking. Except for some range and wildlife research and several general studies (Wells and Shunk 1931; Leukel and St<Jkes 1939; Biswell and Lemon 1943; Burton 1944; Lemon 1949, 1967; Campbell 1955; Biswell1958; Hodgkins 1958; Arata 1959; Cushwa et al. 1966, 1970; Wolters 1972) , most investigators have ignored the herbaceous cover or grassland vegetation under southeastern trees. Even early botanists often became more interested in the unusual botanical features such as the southern extent of Appalachian tree species (Harper 1943, 1952), the description of the silaceous dunes of the 175 RICHARD J. VOGL Gulf Coast (Kurz 1942), the habits of eastern red cedar (Harper 1912), the vegetation of the Okefenokee Swamp (Wright and Wright 1932), or why the Black Belt Prairie of Alabama was treeless (Ranking and Davis 1971), thereby neglecting the widespread and common grassland vegetation and its relationship to fire. -
2007 PEI State of Wildlife Report
State of Wildlife Report 2007 1 State of Wildlife – 2007 Cover photo Tourism PEI, AnnMacNeill Photographer Table of Contents 1.0 Introduction 1 1.1 Background information ......................................1 1.1.1 Location ............................................1 1.1.2 Climate.............................................1 1.1.3 Geology and Soils ....................................1 1.1.4 Land Use ...........................................2 1.1.5 History of Wetlands in Prince Edward Island................3 1.1.6 Rivers and Streams ...................................4 2.0 Habitat 5 2.1 Status of Forests ...........................................5 2.1.1 Forest Inventory......................................5 2.1.2 Forest Communities...................................6 2.2 Status of Fish Habitat ........................................7 2.2.1 Impoundments and Fish Habitat .........................7 2.2.2 Fish Passage ........................................7 2.3 Status of Wetlands ..........................................8 2.3.1 Freshwater Wetlands ..................................8 2.3.2 Coastal Wetlands and Estuaries .........................8 2.4 Status of Sand Dunes ........................................9 2.5 Status of Public Land .......................................10 2.5.1 Public Ponds .......................................10 2.5.2 Provincial Forests ...................................11 2.5.3 Natural Areas .......................................11 2.5.4 Wildlife Management Areas ............................12 2.5.5 -
Native Vascular Flora of the City of Alexandria, Virginia
Native Vascular Flora City of Alexandria, Virginia Photo by Gary P. Fleming December 2015 Native Vascular Flora of the City of Alexandria, Virginia December 2015 By Roderick H. Simmons City of Alexandria Department of Recreation, Parks, and Cultural Activities, Natural Resources Division 2900-A Business Center Drive Alexandria, Virginia 22314 [email protected] Suggested citation: Simmons, R.H. 2015. Native vascular flora of the City of Alexandria, Virginia. City of Alexandria Department of Recreation, Parks, and Cultural Activities, Alexandria, Virginia. 104 pp. Table of Contents Abstract ............................................................................................................................................ 2 Introduction ...................................................................................................................................... 2 Climate ..................................................................................................................................... 2 Geology and Soils .................................................................................................................... 3 History of Botanical Studies in Alexandria .............................................................................. 5 Methods ............................................................................................................................................ 7 Results and Discussion .................................................................................................................... -
INTRODUCTION This Check List of the Plants of New Jersey Has Been
INTRODUCTION This Check List of the Plants of New Jersey has been compiled by updating and integrating the catalogs prepared by such authors as Nathaniel Lord Britton (1881 and 1889), Witmer Stone (1911), and Norman Taylor (1915) with such other sources as recently-published local lists, field trip reports of the Torrey Botanical Society and the Philadelphia Botanical Club, the New Jersey Natural Heritage Program’s list of threatened and endangered plants, personal observations in the field and the herbarium, and observations by other competent field botanists. The Check List includes 2,758 species, a botanical diversity that is rather unexpected in a small state like New Jersey. Of these, 1,944 are plants that are (or were) native to the state - still a large number, and one that reflects New Jersey's habitat diversity. The balance are plants that have been introduced from other countries or from other parts of North America. The list could be lengthened by hundreds of species by including non-persistent garden escapes and obscure waifs and ballast plants, many of which have not been seen in New Jersey since the nineteenth century, but it would be misleading to do so. The Check List should include all the plants that are truly native to New Jersey, plus all the introduced species that are naturalized here or for which there are relatively recent records, as well as many introduced plants of very limited occurrence. But no claims are made for the absolute perfection of the list. Plant nomenclature is constantly being revised. Single old species may be split into several new species, or multiple old species may be combined into one.