DOCSLIB.ORG

HPDL Family Genus Species # Location Collector 4583 D-Aizoaceae Sesuvium Portulacastrum Anaeho'omalu Bay, H C

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
HPDL Family Genus Species # Location Collector 4583 D-Aizoaceae Sesuvium Portulacastrum Anaeho'omalu Bay, H C HPDL Family Genus Species # Location Collector 4583 d-Aizoaceae Sesuvium portulacastrum Anaeho'omalu Bay, H C. Morden 1807 292 d-Aizoaceae Sesuvium portulacastrum Mahai'ula Beach, H Morden 1205 348 d-Aizoaceae Sesuvium portulacastrum Queens Beach, O Morden 1289 4744 d-Aizoaceae Sesuvium portulacastrum W Molokai C. Morden 1959 2105 d-Amaranthaceae Acharanthes splendens var rotundata Kaena Pt., O C. Morden 1574 4710 d-Amaranthaceae Acharanthes splendens var rotundata Kaena Pt., O C. Morden 1917 4562 d-Amaranthaceae Charpentiera obovata Lyon Arboretum* C. Morden 1669 d-Amaranthaceae Charpentiera tomentosa Waianae Kai, O Morden 1531 2172 d-Amaranthaceae Nototrichium humile Waianae Kai, O V. Caraway sn 4590 d-Amaranthaceae Nototrichium sandwicense Amy Greenwell, H* C. Morden 1813 5143 d-Amaranthaceae Nototrichium sandwicense Pu'uWa'awa'a, Hawaii C. Morden 2012 115 d-Amaranthaceae Nototrichium sandwicense So. Kona, H Morden 1096 4591 d-Amaranthaceae Nototrichium Amy Greenwell, H* C. Morden 1814 4668 d-Amaranthaceae Nototrichium 3-Army 4887 4676 d-Amaranthaceae Nototrichium 11-Army 6259 2711 d-Anacardiaceae Rhus sandwicensis Hilo, H 5211 d-Apiaceae Sanicula sandwicensis Maui C. Morden 2067 5476 d-Apocynaceae Alyxia oliviformes Humu'ula Trail, H JL Birch125 4772 d-Apocynaceae Alyxia oliviformes Kokee K C. Morden 1846 377 d-Apocynaceae Alyxia oliviformes Poamoho trail, O Morden 1262 5041 d-Apocynaceae Alyxia oliviformes Waikamoi, eM JL Birch 019 1749 d-Apocynaceae Alyxia oliviformes L89.0875* 612 d-Apocynaceae Ochrosia kilaueaensis Volcanoes, H Motley 1541 2376 d-Apocynaceae Raulwolfia sandwicencis Wailupe Ridge, O C.W. Morden 1613 4706 d-Apocynaceae Rauvolfia sandwicensis Aiea Ridge, O C. Morden 1929 5365 d-Apocynaceae Rauvolfia sandwicensis Kipapa Trail, O LS Reynolds124 5130 d-Apocynaceae Rauvolfia sandwicensis Koa'ia Preserve, H C. Morden 1998 4944 d-Apocynaceae Rauvolfia sandwicensis M JL Birch 036 287 d-Apocynaceae Rauvolfia sandwicensis Waimea, H Morden 1200 2445 d-Apocynaceae Rauvolfia sandwicensis LeGrande sn 5152 d-Apocynaceae Rauvolfia sandwicensis 2157 d-Aquafoliaceae Ilex anomala Hualalei, H C. Morden 1585 4387 d-Aquafoliaceae Ilex anomala Kokee, K A. Sison sn 2441 d-Aquafoliaceae Ilex anomala LeGrande sn 5461 d-Aquifoliaceae Ilex anomala Humu'ula Trail, H JL Birch111 5340 d-Aquifoliaceae Ilex anomala Kipapa Trail, O LS Reynolds095 5235 d-Aquifoliaceae Ilex anomala Koai'a Preserve, H C. Morden 2076 4704 d-Aquifoliaceae Ilex anomola Aiea Ridge C. Morden 1926 5161 d-Aquifoliaceae Ilex anomola Maui C. Morden 2034 5030 d-Aquifoliaceae Ilex anomola Waihe'e Ridge Maui JL Birch 008 4793 d-Araliacae Cheirodendron trigynum (Gand.) Alakai Swamp Trail along boardwalk, ForestedC. Morden area 1877 5400 d-Araliaceae Cheirodendron ? Kipapa Trail, O LS Reynolds198 *Grown in greenhouse or arboreta/botanical garden Page 1 7/2/07 HPDL Family Genus Species # Location Collector 355 d-Araliaceae Cheirodendron platyphyllum Poamoho trail, O Morden 1226 2154 d-Araliaceae Cheirodendron trigynum Hualalei, H C. Morden 1582 5032 d-Araliaceae Cheirodendron trigynum Waihe'e Ridge Maui JL Birch 010 2443 d-Araliaceae Cheirodendron trigynum LeGrande sn 2444 d-Araliaceae Cheirodendron trigynum LeGrande sn 5240 d-Araliaceae Cheirodendron trigynum platyphylla ssp. triginum Koai'a Preserve, H C. Morden 2081 5165 d-Araliaceae Cheirodendron Maui C. Morden 2038 3225 d-Araliaceae Munroidendron racemosum Allerton Bridge NTBG (no number) 2446 d-Araliaceae Munroidendron racemosum cultivated LeGrande sn 3249 d-Araliaceae Munroidendron racemosum 1 Eastern drainage, K* NTBG 990871 3250 d-Araliaceae Munroidendron racemosum 2 Eastern drainage, K* NTBG 990871 3251 d-Araliaceae Munroidendron racemosum 3 Eastern drainage, K* NTBG 990871 3252 d-Araliaceae Munroidendron racemosum 4 Eastern drainage, K* NTBG 990871 3253 d-Araliaceae Munroidendron racemosum 5 Eastern drainage, K* NTBG 990871 3244 d-Araliaceae Munroidendron racemosum 1 Hoolulu Stream, K* NTBG 990812.001 3245 d-Araliaceae Munroidendron racemosum 2 Hoolulu Stream, K* NTBG 990812.007 3246 d-Araliaceae Munroidendron racemosum 3 Hoolulu Stream, K* NTBG 990812-1 3247 d-Araliaceae Munroidendron racemosum 4 Hoolulu Stream, K* NTBG 990812-2 3248 d-Araliaceae Munroidendron racemosum 5 Hoolulu Stream, K* NTBG 990812-3 3254 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990872.016 3255 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990873 3256 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990873 3257 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990873 3258 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990873 3259 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990873 3260 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990874 3261 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990874 3262 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990874 3263 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990874 3264 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990874 3265 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990875 3266 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990875 3267 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990875 3268 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990875 3269 d-Araliaceae Munroidendron racemosum Kalalau, Nakeik., K* NTBG 990875 3328 d-Araliaceae Munroidendron racemosum Kawai‘iki Canyon, K KR Wood 9158 3231 d-Araliaceae Munroidendron racemosum Kipu Kai Valley, K* NTBG 000645 3232 d-Araliaceae Munroidendron racemosum Kipu Kai Valley, K* NTBG 000645 3233 d-Araliaceae Munroidendron racemosum Kipu Kai Valley, K* NTBG 000645 3234 d-Araliaceae Munroidendron racemosum Kipu Kai Valley, K* NTBG 000645 3235 d-Araliaceae Munroidendron racemosum Kipu Kai Valley, K* NTBG 000645 3280 d-Araliaceae Munroidendron racemosum Kipu Kai Valley, K* NTBG 990936 *Grown in greenhouse or arboreta/botanical garden Page 2 7/2/07 HPDL Family Genus Species # Location Collector 3281 d-Araliaceae Munroidendron racemosum Kipu Kai Valley, K* NTBG 990936 3282 d-Araliaceae Munroidendron racemosum Kipu Kai Valley, K* NTBG 990936 3283 d-Araliaceae Munroidendron racemosum Kipu Kai Valley, K* NTBG 990936 3284 d-Araliaceae Munroidendron racemosum Kipu Kai Valley, K* NTBG 990936 3226 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 000379 3227 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 000379 3228 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 000379 3229 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 000379 3230 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 000379 3236 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 910034.007 3237 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 910034.010 3238 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 910034.019 3239 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 910034.023 3240 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 910244.001 3241 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 910245.001 3242 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 910245.002 3243 d-Araliaceae Munroidendron racemosum Lawai, K* NTBG 930352.004 3431 d-Araliaceae Munroidendron racemosum Maui Nui Botanical Garden 3270 d-Araliaceae Munroidendron racemosum 1 Nakeikionaiwi, K* NTBG 990876 3271 d-Araliaceae Munroidendron racemosum 2 Nakeikionaiwi, K* NTBG 990876 3272 d-Araliaceae Munroidendron racemosum 3 Nakeikionaiwi, K* NTBG 990876 3273 d-Araliaceae Munroidendron racemosum 4 Nakeikionaiwi, K* NTBG 990876 3274 d-Araliaceae Munroidendron racemosum 5 Nakeikionaiwi, K* NTBG 990876 3334 d-Araliaceae Munroidendron racemosum NTBG* Motley green 3335 d-Araliaceae Munroidendron racemosum NTBG* Motley red 3275 d-Araliaceae Munroidendron racemosum 1 Pohakuao gulch, K* NTBG 990877 3276 d-Araliaceae Munroidendron racemosum 2 Pohakuao gulch, K* NTBG 990877 3277 d-Araliaceae Munroidendron racemosum 3 Pohakuao gulch, K* NTBG 990877 3278 d-Araliaceae Munroidendron racemosum 4 Pohakuao gulch, K* NTBG 990877 3279 d-Araliaceae Munroidendron racemosum 5 Pohakuao gulch, K* NTBG 990877 3217 d-Araliaceae Munroidendron racemosum Pohakuao, K K. R. Wood 9084 4984 d-Araliaceae Reynoldsia sandwicense KNARS, M JL Birch 039 2514 d-Araliaceae Reynoldsia sandwicense Kona, H Morden 1623 2378 d-Araliaceae Tetraplansandra oahuensis Kulepeamoa Ridge, O C.W. Morden 1612 1750 d-Araliaceae Tetraplasandra lydgatei L98.0059* 1310 d-Araliaceae Tetraplasandra oahuensis Palikea Trail, O V. Caraway 20 5033 d-Araliaceae Tetraplasandra oahuensis Waihe'e Ridge Maui JL Birch 011 5159 d-Araliaceae Tetraplasandra Maui C. Morden 2032 4813 d-Araliaceae Tetraplasandra Nualolo Trail, Kokee St. Park C. Morden 1905 1100 d-Asclepidaceae Hoya sp. 1565 d-Asteraceae Argy X Dubautia sandw. X ciliolata Waipahoehoe Gulch, H Morden 1520 1189 d-Asteraceae Argy. x Dub. kauense x scabra (put) Mauna Loa, H AK x DSCS *Grown in greenhouse or arboreta/botanical garden Page 3 7/2/07 HPDL Family Genus Species # Location Collector 1192 d-Asteraceae Argyr. x Dub. caligens x laxa Eke, W. M. Carr 1457 1201 d-Asteraceae Argyr. x Dub. grayanum x plant. (put) pu'ukukui, W. M. Carr 1461 1099 d-Asteraceae Argyroxiphium sandwicense ssp m. Haleakala, M G. Carr 1494 321 d-Asteraceae Artemisia australis Hawaii Kai, O Morden 1217 4713 d-Asteraceae Artemisia australis Kaena Pt. Nat Area Reserve C. Morden 1920 2104 d-Asteraceae Artemisia australis Kaena Pt., O C. Morden 1573 5249 d-Asteraceae Artemisia australis
Load more

Recommended publications
  • Commercial Use of Native Hawaiian Plants Laws and Requirements for the Propagation and Sale of Threatened and Endangered Hawaiian Plant Species
    College of Tropical Agriculture cooperative Extension PUBLICATIONS and Human Resources University of Hawai‘i at manoa Commercial Use of Native Hawaiian Plants Laws and Requirements for the Propagation and Sale of Threatened and Endangered Hawaiian Plant Species Introduction • Find here an ESA fact sheet (fws.gov/endangered/esa- library/pdf/ESA_basics.pdf). The Endangered Species Act (ESA) was passed by the U.S. Congress in 1973 to help prevent the extinction of • Here is a current list of T&E plants of Hawai‘i (fws.gov/ rare species. More than one-fourth of Hawai‘i’s native endangered/?ref=topbar). plants are listed as threatened (T, likely to become endan- The FWS works in conjunction with the State of Hawai‘i’s gered) or endangered (E, in danger of extinction). Native Department of Land and Natural Resources (DLNR), plants are those whose ancestors arrived on the Hawaiian Division of Forestry and Wildlife (DOFAW) to administer Islands millions Permit Guidelines (dlnr.hawaii.gov/ecosystems/rare-plants/ of years ago by permits) that allow activities involving rare, threatened, or wind, waves, or endangered plants. wings. Most are endemic, and Why Use Native T&E Plants? evolved in Ha- wai‘i’s isolated Endemic (found only in Hawai‘i) and indigenous (also ecosystem into native elsewhere) plants have aesthetic, cultural, and species found recreational values that are integral to what makes nowhere else in Hawai‘i Hawai‘i. the world. These plants are adapted to Hawai‘i’s environment. Once With hundreds established in a suitable habitat, with the proper climate of plants on the and soils, they will require less water, fertilizer, and Threatened & maintenance than non-native plants.
    [Show full text]
  • Nototrichium Humile
    16-122 2 16.20 Taxon Summary: Nototrichium humile 4 Photographer: Hawaii Natural Heritage Program 6 Scientific name: Nototrichium humile Hillebr. Hawaiian name: Kului 8 Family: Amaranthaceae (Amaranth family) Federal status: Listed endangered 10 Description and biology: Nototrichium humile is a perennial basal-branching shrub with 12 upright or arching branches. The plant is typically 1-2 m (3.3-6.6 ft) tall. Its leaves are ovate to oblong, measure 3-9 cm (1.2-3.5 in) long, and are green (unlike the other two species of 14 Nototrichium, whose leaves are covered with silvery hairs). The spikes are slender, measure 3- 14 cm (1.2-5.5 in) long, and hang down as they lengthen. The flowers are small and 16 inconspicuous, and perfect (possessing both male and female reproductive parts). The fruits are not much larger than the flowers. 18 Flowering is generally heaviest in the spring and summer. It is not known if the plants are self- 20 compatible. Pollination vectors for the species are unknown. The fruits mature a few weeks after flowering. The seeds have no obvious dispersal mechanisms. Based on observations of 22 particular individuals of this species, the plants live for at least one or two decades (Lau pers. comm. 2000). 24 Known distribution: Nototrichium humile occurs in the Waianae Mountains of Oahu, where it 26 found throughout the mountain range, on both the windward and leeward sides. The only record of the species beyond the Waianae Mountains is a specimen collected in the 1970s on the south 28 slope of Haleakala, Maui.
    [Show full text]
  • Rethinking Phylogenetics Using Caryophyllales (Angiosperms), Matk Gene and Trnk Intron As Experimental Platform
    Rethinking phylogenetics using Caryophyllales (angiosperms), matK gene and trnK intron as experimental platform Sunny Sheliese Crawley Dissertation submitted to the faculty of the Virginia Polytechnic Institute and State University in partial fulfillment of the requirements for the degree of Doctor of Philosophy In Biological Sciences Khidir W. Hilu Eric P. Beers Carla V. Finkielstein Jill C. Sible December 2, 2011 Blacksburg, Virginia Keywords: (phylogeny, missing data, caryophyllids, trnK intron, matK, RNA editing, gnetophytes) Copyright 2011, Sunny Sheliese Crawley Rethinking phylogenetics using Caryophyllales (angiosperms), matK gene and trnK intron as experimental platform Sunny Sheliese Crawley ABSTRACT The recent call to reconstruct a detailed picture of the tree of life for all organisms has forever changed the field of molecular phylogenetics. Sequencing technology has improved to the point that scientists can now routinely sequence complete plastid/mitochondrial genomes and thus, vast amounts of data can be used to reconstruct phylogenies. These data are accumulating in DNA sequence repositories, such as GenBank, where everyone can benefit from the vast growth of information. The trend of generating genomic-region rich datasets has far outpaced the expasion of datasets by sampling a broader array of taxa. We show here that expanding a dataset both by increasing genomic regions and species sampled using GenBank data, despite the inherent missing DNA that comes with GenBank data, can provide a robust phylogeny for the plant order Caryophyllales (angiosperms). We also investigate the utility of trnK intron in phylogeny reconstruction at relativley deep evolutionary history (the caryophyllid order) by comparing it with rapidly evolving matK. We show that trnK intron is comparable to matK in terms of the proportion of variable sites, parsimony informative sites, the distribution of those sites among rate classes, and phylogenetic informativness across the history of the order.
    [Show full text]
  • Federally Listed Species Occurring in the U.S
    Federally Listed Species Occurring in the U.S. Fish and Wildlife Service’s Pacific Region Region 1, Recovery Permit TE-702631-29 Common Name Scientific Name Listing Status Mammals Rabbit, Columbia Basin pygmy Brachylagus idahoensis E Wolf, gray Canis lupus E Bat, Pacific sheath-tailed (Mariana Emballonura semicaudata rotensis E subspecies) Bat, Pacific sheath-tailed (South Emballonura semicaudata semicaudata E Pacific subspecies) Bat, Hawaiian hoary Lasiurus cinereus semotus E Lynx, Canada Lynx canadensis T Deer, Columbian white-tailed Odocoileus virginianus leucurus T Bat, Mariana fruit (=Mariana flying Pteropus mariannus mariannus T fox) Bat, little Mariana fruit Pteropus tokudae E Caribou, woodland Rangifer tarandus caribou E Pocket gopher, Roy Prairie Thomomys mazama glacialis T Pocket gopher, Olympia Thomomys mazama pugetensis T Pocket gopher, Tenino Thomomys mazama tumuli T Pocket gopher, Yelm Thomomys mazama yelmensis T Squirrel, northern Idaho ground Urocitellus brunneus T Bear, grizzly Ursus arctos horribilis T Birds Millerbird, Nihoa (old world Acrocephalus familiaris kingi E warbler) Warbler, nightingale reed (old world Acrocephalus luscinia E warbler) Swiftlet, Mariana gray Aerodramus vanikorensis bartschi E Akialoa, Kauai (honeycreeper) Akialoa stejnegeri E Duck, Laysan Anas laysanensis E Duck, Hawaiian (=koloa) Anas wyvilliana E Murrelet, marbled Brachyramphus marmoratus T Goose, Hawaiian Branta (=Nesochen) sandvicensis E Hawk, Hawaiian (='lo) Buteo solitarius E Plover, western snowy Charadrius alexandrinus nivosus T Elepaio,
    [Show full text]
  • Phylogeny and Morphological Evolution of the Chenopodiaceae-Amaranthaceae Alliance Donald B
    Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 2003 Phylogeny and morphological evolution of the Chenopodiaceae-Amaranthaceae alliance Donald B. Pratt Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Botany Commons, and the Genetics Commons Recommended Citation Pratt, Donald B., "Phylogeny and morphological evolution of the Chenopodiaceae-Amaranthaceae alliance " (2003). Retrospective Theses and Dissertations. 613. https://lib.dr.iastate.edu/rtd/613 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand comer and continuing from left to right in equal sections with small overlaps.
    [Show full text]
  • Phylogenetic Analyses of Amaranthaceae Based on Matk DNA Sequence Data with Emphasis on West African Species
    Turk J Bot Research Article 33 (2009) 153-161 © TÜBİTAK doi:10.3906/bot-0707-15 Phylogenetic Analyses of Amaranthaceae Based on matK DNA Sequence Data with Emphasis on West African Species Oluwatoyin T. OGUNDIPE1,*, Mark CHASE2 1Department of Botany and Microbiology, University of Lagos, Akoka, Lagos, NIGERIA 2Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, UK Received: 19.07.2007 Accepted: 28.04.2009 Abstract: Comparative sequencing of the chloroplast matK coding and non-coding regions was used to examine relationship among the species of Amaranthaceae with emphasis on the West African species and other closely related family such as Chenopodiaceae, Portulacaceae, and Caryophyllaceae. Phylogenetic analysis of the matK sequences alone and in combination using maximum parsimony methods produced monophyletic lineage of Amaranthaceae-Chenopodiaceae. Our results indicated that a polyphyletic Celosieae as sister to an Amaranthus-Chemissoa lineage. Subfamily Amaranthoideae is paraphyletic to the core Gomphrenoids. This study also shows that the polyphyly of Amarantheae is apparent and so is the polyphyly of Amaranthinae. Key Words: Amaranthaceae, matK, Phylogenetic analyses Introduction Amaranthaceae and Chenopodiaceae are similar in Amaranthaceae, commonly called the Amaranth their morphology, anatomy, and phytochemistry (Brown, family, contains about 65 genera and 900 species. They 1810; Bentham & Hooker, 1880; Baillo, 1887; Volkens, are widespread and cosmopolitan in distribution but most 1893; Carolin, 1983; Kuhn et al., 1993; Townsend, abundant in tropics, subtropics, and warm-temperate 1993). Furthermore, based on serological studies, it is regions, evidently absent from alpine and arctic regions. believed that Amaranthaceae and the related sister family Centres of diversity for Amaranthaceae are south-western Chenopodiaceae should be merged together (Baillon, North America, Central America, South America, and 1887 & Mallingson, 1922).
    [Show full text]
  • Revised Determinations of Prudency and Proposed Designations of Critical Habitat for Plant Species from the Islands of Kauai and Niihau, Hawaii; Proposed Rule
    Monday, January 28, 2002 Part II Department of the Interior Fish and Wildlife Service 50 CFR Part 17 Endangered and Threatened Wildlife and Plants; Revised Determinations of Prudency and Proposed Designations of Critical Habitat for Plant Species From the Islands of Kauai and Niihau, Hawaii; Proposed Rule VerDate 11<MAY>2000 22:02 Jan 25, 2002 Jkt 197001 PO 00000 Frm 00001 Fmt 4717 Sfmt 4717 E:\FR\FM\28JAP2.SGM pfrm01 PsN: 28JAP2 3940 Federal Register / Vol. 67, No. 18 / Monday, January 28, 2002 / Proposed Rules DEPARTMENT OF THE INTERIOR critical habitat for nine of these species proposed for three species of loulu (Ctenitis squamigera, Diellia erecta, palm, Pritchardia aylmer-robinsonii, P. Fish and Wildlife Service Diplazium molokaiense, Hibiscus napaliensis, and P. viscosa for which we brackenridgei, Ischaemum byrone, determined, on November 7, 2000, that 50 CFR Part 17 Mariscus pennatiformis, Phlegmariurus critical habitat designation is not RIN 1018–AG71 manni, Silene lanceolata, and Vigna o- prudent because it would likely increase wahuensis) in other proposed rules the threats from vandalism or collection Endangered and Threatened Wildlife published on December 18, 2000 (Maui of these species on Kauai and Niihau, and Plants; Revised Determinations of and Kahoolawe), on December 27, 2000 and no change is made to that Prudency and Proposed Designations (Lanai), and on December 29, 2000 determination here. Critical habitat is of Critical Habitat for Plant Species (Molokai). In this proposal we not proposed for two species, Melicope From the Islands of Kauai and Niihau, incorporate the prudency quadrangularis and Acaena exigua, for Hawaii determinations for these nine species which we determined, on November 7, and propose designation of critical 2000, and December 18, 2000, AGENCY: Fish and Wildlife Service, habitat for Ctenitis squamigera, Diellia respectively, that critical habitat was not Interior.
    [Show full text]
  • Disparity, Diversity, and Duplications in the Caryophyllales
    Research Disparity, diversity, and duplications in the Caryophyllales Stephen A. Smith1, Joseph W. Brown1, Ya Yang2, Riva Bruenn3, Chloe P. Drummond3, Samuel F. Brockington4, Joseph F. Walker1, Noah Last2, Norman A. Douglas3 and Michael J. Moore3 1Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI 48103, USA; 2Department of Plant Biology, University of Minnesota-Twin Cities, 1445 Gortner Avenue, St Paul, MN 55108, USA; 3Department of Biology, Oberlin College, 119 Woodland St, Oberlin, OH 44074-1097, USA; 4Department of Plant Sciences, University of Cambridge, Cambridge, CB2 3EA, UK Summary Author for correspondence: The role played by whole genome duplication (WGD) in plant evolution is actively debated. Stephen A. Smith WGDs have been associated with advantages such as superior colonization, various adapta- Tel: +1 734 615 5510 tions, and increased effective population size. However, the lack of a comprehensive mapping Email: [email protected] of WGDs within a major plant clade has led to uncertainty regarding the potential association Received: 30 May 2017 of WGDs and higher diversification rates. Accepted: 28 July 2017 Using seven chloroplast and nuclear ribosomal genes, we constructed a phylogeny of 5036 species of Caryophyllales, representing nearly half of the extant species. We phylogenetically New Phytologist (2017) mapped putative WGDs as identified from analyses on transcriptomic and genomic data and doi: 10.1111/nph.14772 analyzed these in conjunction with shifts in climatic occupancy and lineage diversification rate. Thirteen putative WGDs and 27 diversification shifts could be mapped onto the phylogeny. Key words: Caryophyllales, climatic occupancy, diversification rates, duplications, Of these, four WGDs were concurrent with diversification shifts, with other diversification phylogenomics.
    [Show full text]
  • What Is the Evidence That Invasive Species Are a Significant Contributor to the Decline Or Loss of Threatened Species? Philip D
    Invasive Species Systematic Review, March 2015 What is the evidence that invasive species are a significant contributor to the decline or loss of threatened species? Philip D. Roberts, Hilda Diaz-Soltero, David J. Hemming, Martin J. Parr, Richard H. Shaw, Nicola Wakefield, Holly J. Wright, Arne B.R. Witt www.cabi.org KNOWLEDGE FOR LIFE Contents Contents .................................................................................................................................. 1 Abstract .................................................................................................................................... 3 Keywords ................................................................................................................................. 4 Definitions ................................................................................................................................ 4 Background .............................................................................................................................. 5 Objective of the review ............................................................................................................ 7 The primary review question: ....................................................................................... 7 Secondary question 1: ................................................................................................. 7 Secondary question 2: ................................................................................................. 7 Methods
    [Show full text]
  • Nototrichium Humile (Kulu'i)
    Nototrichium humile (Kulu'i) 5-Year Review Summary and Evaluation U.S. Fish and Wildlife Service Pacific Islands Fish and Wildlife Office Honolulu, Hawaii 5-YEAR REVIEW Species reviewed: Nototrichium humile (Kulu'i) TABLE OF CONTENTS 1.0 GENERAL INFORMATION 1 1.1 Reviewers 1 1.2 Methodology used to complete the review 1 1.3 Background 1 2.0 REVIEW ANALySIS 3 2.1 Application of the 1996 Distinct Population Segment (DPS) policy 3 2.2 Recovery Criteria 3 2.3 Updated Information and Current Species Status 4 2.4 Synthesis 6 3.0 RESULTS 8 3.1 Recommended Classification 8 3.2 New Recovery Priority Number 8 3.3 Listing and Reclassification Priority Number 8 4.0 RECOMMENDATIONS FOR FUTURE ACTIONS 9 5.0 REFERENCES 9 Signature Page 11 2 5-YEAR REVIEW Notrotrichium humile (Knln'i) 1.0 GENERAL INFORMATION 1.1 Reviewers Lead Regional Office: Region 1, Jesse D'Elia, Chief, Division of Recovery, (503) 231-2071 Lead Field Office: Pacific Islands Fish and Wildlife Office, Gina Shultz, Assistant Field Supervisor for Endangered Species, (808) 792-9400 Cooperating Field Office(s): N/A Cooperating Regional Office(s): N/A 1.2 Methodology used to complete the review: This review was conducted by staff ofthe Pacific Islands Fish and Wildlife Office (PIFWO) ofthe U.S. Fish and Wildlife Service (USFWS) between June 2006 and September 2007. The Hawaii Biodiversity and Mapping Program provided most of the updated information on the current status ofNototrichium humile. They also provided recommendations for conservation actions that may be needed prior to the next five-year review.
    [Show full text]
  • STATUS of the NATIVE FLOWERING PLANTS of the HAWAIIAN ISLANDS Warren L
    2. STATUS OF THE NATIVE FLOWERING PLANTS OF THE HAWAIIAN ISLANDS Warren L. Wagner Derral R. Herbst and Rylan S.N. Yee ABSTRACT Estimates of the total number of native Hawaiian plants are widely divergent because of differences in species concepts; our evaluation suggests 1,200-1,300 native species. Hawaifi has the highest number of can- didate threatened and endangered plants for the United States (31%), with approximately 10% of the native flowering plants already extinct. Although a modern taxonomic review of the Hawaiian flora will reduce the number of taxa considered valid, roughly 50% of the flora will still be considered threatened or endan- gered. Currently 11 Hawaiian plants are listed as en- dangered, one has been proposed as endangered, and the documentation for an additional 9 is currently under review. An evaluation comparing the number of candidate taxa on each island and in each major ecological zone shows that the islands with the highest percentages of candidate taxa are O'ahu (27.3%), followed by Hawai'i (18.3%), Maui (16.8%), and Kauafi (14%). The low num- bers on islands such as Ni*ihau (1.5%) and Kaho'olawe (0.7%) are apparently partly a reflection of the loss of most of the native vegetation prior to study of these islands, and partly because of lower physio- graphic diversity. The ecological zones most severely degraded are mixed mesophytic forest, which harbors nearly 33% of the total candidate taxa, and low eleva- tion rain forest with 24%. Not indicated by this anal- ysis is the severe degradation of lowland vegetation (with 14% of total candidate taxa) and coastal vegeta- tion (with 9.5%) that occurred prior to their scientif- ic study.
    [Show full text]
  • Temperate Eurasian Origins of Hawaiian Chenopodium (Amaranthaceae) Plus Description of a New Species Endemic to Moloka‘I
    Bucknell University Bucknell Digital Commons Faculty Journal Articles Faculty Scholarship 2020 Temperate Eurasian Origins of Hawaiian Chenopodium (Amaranthaceae) plus description of a new species endemic to Moloka‘i Jason T. Cantley San Francisco State University Angela J. McDonnell Bucknell University J Branson San Francisco State University S R. Long Bucknell University W Garnett See next page for additional authors Follow this and additional works at: https://digitalcommons.bucknell.edu/fac_journ Part of the Biodiversity Commons, Botany Commons, Evolution Commons, Integrative Biology Commons, Molecular Genetics Commons, and the Terrestrial and Aquatic Ecology Commons Recommended Citation 33. Cantley, J.T., A.J. McDonnell, J. Branson, J. Kobara, S.R. Long, W. Garnett and C.T. Martine. 2020. Temperate Eurasian Origins of Hawaiian Chenopodium (Amaranthaceae) plus description of a new species endemic to Moloka‘i. Systematic Botany 45(3), 554-566. This Article is brought to you for free and open access by the Faculty Scholarship at Bucknell Digital Commons. It has been accepted for inclusion in Faculty Journal Articles by an authorized administrator of Bucknell Digital Commons. For more information, please contact [email protected]. Authors Jason T. Cantley, Angela J. McDonnell, J Branson, S R. Long, W Garnett, and Christopher T. Martine This article is available at Bucknell Digital Commons: https://digitalcommons.bucknell.edu/fac_journ/1729 Temperate Eurasian Origins of Hawaiian Chenopodium (Amaranthaceae), Plus Description of a New
    [Show full text]