Flaming Fabaceae —Using an Alcohol Flame to Break Seed Dormancy
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RESTORATION Summary
Kahoʻolawe Island Reserve Commission 1. RESTORATION Summary DOH Restoration Project Status Update (July 1 to Sept 30, 2019) In July 2019 the Kamehameha School teachers came out to island to outplant the last 1609 plants for a total of 10,000 in the project site. They constructed the last wattles and installed irrigation. Kamehameha School Teachers installing a wattle with native plants and irrigation. The finished wattle product with native plants on irrigation in the project site Jamie also installed a pressure reducing valve on the 1” Sub Main to reduce the pressure buildup in the line from gravity. The map illustrates the end result of wattles, native plants and irrigation installed in the DOH Project Site. Wattles, native plants and irrigation installed in the DOH project site A pressure reducing valve on the 1” sub main to alleviate high pressure blow outs in the irrigation line. Jamie also captured the secondary drone images an altitude of 50’ to compare to the original images taken in 2018. Some of the comparisons showed the installation of wattles with vegetation. Drone Image #7 2018 Drone Image #7 2019 Drone Image #7 2019 shows the installation of a wattle on the hard pan. The 1 year DOH Project was completed on August 9, 2019 and 200 volunteers put in 10,000 native plants. Although the success rate was low due to a relatively dry year, the infrastructure has been installed for future potential maintenance. Jamie operating the DJI Phantom Drone in the DOH Project Site Below are examples of before and after photopoints (#7 East West and South) in the DOH Project Site showing the additions of the wattles made from burlap and native vegetation on irrigation. -
Pu'u Wa'awa'a Biological Assessment
PU‘U WA‘AWA‘A BIOLOGICAL ASSESSMENT PU‘U WA‘AWA‘A, NORTH KONA, HAWAII Prepared by: Jon G. Giffin Forestry & Wildlife Manager August 2003 STATE OF HAWAII DEPARTMENT OF LAND AND NATURAL RESOURCES DIVISION OF FORESTRY AND WILDLIFE TABLE OF CONTENTS TITLE PAGE ................................................................................................................................. i TABLE OF CONTENTS ............................................................................................................. ii GENERAL SETTING...................................................................................................................1 Introduction..........................................................................................................................1 Land Use Practices...............................................................................................................1 Geology..................................................................................................................................3 Lava Flows............................................................................................................................5 Lava Tubes ...........................................................................................................................5 Cinder Cones ........................................................................................................................7 Soils .......................................................................................................................................9 -
Origin of Hawaiian Endemic Species of Canavalia (Fabaceae) from Sea-Dispersed Species Revealed by Chloroplast and Nuclear DNA Sequences
J. Jpn. Bot. 86: 15–25 (2011) Origin of Hawaiian Endemic Species of Canavalia (Fabaceae) from Sea-Dispersed Species Revealed by Chloroplast and Nuclear DNA Sequences a a,† b Mohammad VATANPARAST , Koji TAKAYAMA , Mario S. SOUSA , Yoichi c a, TATEISHI and Tadashi KAJITA * aDepartment of Biology, Graduate School of Science, Chiba University, 1-33, Yayoi, Inage, Chiba, 263-8522 JAPAN; bDepartamento de Botánica, Instituto de Biología, Universidad Nacional Autónoma de México, Apartado Postal 70-367, 04510 México, D. F., MÉXICO; cFaculty of Education, University of the Ryukyus, 1, Senbaru, Nishihara, Okinawa, 903-0129 JAPAN; †Present address: Department of Plant Systematics and Evolution, Institute of Botany, University of Vienna. Rennweg 14, A-1030 Wien, AUSTRIA *Corresponding author: [email protected] (Accepted on July 22, 2010) To reveal the origin of the Hawaiian endemic Canavalia species, phylogenetic analyses of chloroplast DNA (cpDNA) and internal transcribed spacers (ITS) of nuclear ribosomal DNA (nrDNA) sequences were performed. Phylogenetic analyses of 6 cpDNA regions (6386 bp) and of nrDNA ITS (708 bp) for all 6 species of the Hawaiian endemic subgenus Maunaloa together with samples from the other 3 subgenera of Canavalia suggested that subgenus Maunaloa is monophyletic and more closely related to subgenus Canavalia than to other subgenera. Phylogenetic analyses of multiple haplotypes of the nrDNA ITS suggested that the Hawaiian endemic species of Canavalia originated from a sea-dispersed species of subgenus Canavalia, possibly Canavalia rosea (Sw.) DC., which is a pantropical species whose seeds are spread by sea drift. A single origin for subgenus Maunaloa might be also suggested. Key words: Canavalia, chloroplast DNA, Hawaiian Islands, nrDNA ITS, phylogeny, seed dispersal. -
Annual Rings in a Native Hawaiian Tree, Sophora Chrysophylla, on Maunakea
TITLE: Annual rings in a native Hawaiian tree, Sophora chrysophylla, on Maunakea, Hawaiʻi RUNNING TITLE: Annual tree-rings in Hawaiʻi KEY WORDS: chronology, crossdating, dendrochronology, māmane, tree age, tree- rings, tropics AUTHORS: Kainana S. Francisco1,2, Patrick J. Hart1,3, Jinbao Li4, Edward R. Cook5, Patrick J. Baker6 INSTITUTIONS: 1Tropical Conservation Biology and Environmental Science, University of Hawaiʻi at Hilo, 200 West Kāwili Street, Hilo, Hawaiʻi, 96720, U.S.A. 2USDA Forest Service, Pacific Southwest Research Station, Institute of Pacific Islands Forestry, 60 Nowelo Street, Hilo, Hawaiʻi, 96720, U.S.A. 3Biology Department, University of Hawaiʻi at Hilo, 200 West Kāwili Street, Hilo, Hawaiʻi, 96720, U.S.A. 4Department of Geography, University of Hong Kong, Pokfulam, Hong Kong 5Tree-Ring Lab, Lamont-Doherty Earth Observatory, Columbia University, 61 Route 9W – PO Box 1000, Palisades, New York, 10964, U.S.A. 6Department of Forest and Ecosystem Science, University of Melbourne, Richmond, Victoria 3121, Australia CORRESPONDING AUTHOR: Kainana S. Francisco, email: [email protected] ABSTRACT Annual rings are not commonly produced in tropical trees because they grow in a relatively aseasonal environment. However, in the subalpine zones of Hawaiʻi’s highest volcanoes, there is often strong seasonal variability in temperature and rainfall. Using classical dendrochronological methods, annual growth rings were shown to occur in Sophora chrysophylla, commonly called māmane, a native tree species on Maunakea, Hawaiʻi. Sampling occurred at three sites on various facing slopes of Maunakea – Puʻulāʻau (west), Pōhakuloa (south), and Puʻumali (north). Chronologies established from nearby non-native, live conifer trees were used to verify the dates from a total of 52 series from 22 S. -
Aspects of House Finch Breeding Biology in Hawaii
ASPECTS OF HOUSE FINCH BREEDING BIOLOGY IN HAWAII CHARLES VAN RIPER III Bent (1968) summarized information avail- Puu Laau, is the last remaining major mamane-naio able on the breeding biology of the House forest in Hawaii. Finch ( Curpodacus mexicanus). Although The stippled areas of figure 1 represent a broad spectrum of the forest types on the island of Hawaii; this species has been studied quite extensively included are native, introduced, and mixed stands of in its North American home range, little atten- vegetation. Areas 2, 3, and 5 are dry forest regions tion has been paid to it in Hawaii. Grinnell with annual rainfall of 76 cm or less; Puu Laau (2) (1911) reported on different color patterns of has mean annual rainfall of 50 cm, Puu Waawaa (3) 64 cm, and Puu Lehua (5) has 76 cm. The Kohala the House Finch in Hawaii, and Richardson Mountain complex ( 1) has a mean annual rainfall of and Bowles (1964) mentioned that on 23 June 229 cm, Puu 00 (4) has 483 cm, and the Kulani- 1960 they found a nestling that had fallen from Mauna Loa complex (6) has 317 cm. its nest on Kauai. On Mauna Kea, Berger Birds were mist-netted, color-banded, and released (1972) found House Finch nests with eggs from 1971 through 1973. Nest and tree heights were taken with a clinometer when it was impractical to as early as 6 April (1968) and as late as 17 use a tape measure. Nests and eggs were measured July (1967). Eleven nests were built on hori- with calipers and weighed on a sensitive spring bal- zontal branches of mamane (Sophora chryso- ance. -
Canavalia Rosea Click on Images to Enlarge
Species information Abo ut Reso urces Hom e A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Canavalia rosea Click on images to enlarge Family Fabaceae Scientific Name Canavalia rosea (Sw.) DC. Candolle, A.P. de (1825) Prodromus 2: 404. Common name Flowers. Copyright Barry Jago Bean, Beach; Coastal Jack Bean; Bean, Coastal Jacl; Bean, Mackenzie; Coastal Canavalia; Canavalia, Coastal; Beach Bean; Bean, Beach; Fire Bean; Mackenzie Bean Stem A slender vine not exceeding a stem diameter of 2 cm. Leaves Middle leaflet blade about 6.3-7 x 5-6.2 cm, stalk about 2.5-3.5 cm long, grooved on the upper surface. Lateral leaflet blades about 5.5-7.4 x 3.5-4.8 cm on stalks about 0.3-0.5 cm long. Compound leaf petiole about 3.5-5.2 cm long, grooved on the upper surface. Stipules caducous. Stipels about 2.5-3 mm long. Lateral Fruits. Copyright CSIRO veins forming loops inside the blade margin. Flowers Racemes longer than the leaves. Flowers about 20-25 mm diam. at anthesis. Calyx tube about 12-14 mm long, lobes of unequal size, about 1.6-3.5 mm long. Petals: standard about 25 mm long; wings and keel about 23 mm long. Stamens 10, all filaments +/- fused to form a tube about 15-18 mm long with free filaments projecting above the tube. Free filaments about 3-6 mm long, alternately longer and shorter. Ovary elongated, densely clothed in appressed pale (whitish) hairs. -
Recovery Plan for Tyoj5llllt . I-Bland Plants
Recovery Plan for tYOJ5llllt. i-bland Plants RECOVERY PLAN FOR MULTI-ISLAND PLANTS Published by U.S. Fish and Wildlife Service Portland, Oregon Approved: Date: / / As the Nation’s principal conservation agency, the Department of the Interior has responsibility for most ofour nationally owned public lands and natural resources. This includes fostering the wisest use ofour land and water resources, protecting our fish and wildlife, preserving the environmental and cultural values ofour national parks and historical places, and providing for the enjoyment of life through outdoor recreation. The Department assesses our energy and mineral resources and works to assure that their development is in the best interests ofall our people. The Department also has a major responsibility for American Indian reservation communities and for people who live in island Territories under U.S. administration. DISCLAIMER PAGE Recovery plans delineate reasonable actions that are believed to be required to recover and/or protect listed species. Plans are published by the U.S. Fish and Wildlife Service, sometimes prepared with the assistance ofrecovery teams, contractors, State agencies, and others. Objectives will be attained and any necessary funds made available subject to budgetary and other constraints affecting the parties involved, as well as the need to address other priorities. Costs indicated for task implementation and/or time for achievement ofrecovery are only estimates and are subject to change. Recovery plans do not necessarily represent the views nor the official positions or approval ofany individuals or agencies involved in the plan formulation, otherthan the U.S. Fish and Wildlife Service. They represent the official position ofthe U.S. -
Downloadable Data Collection
Smetzer et al. Movement Ecology (2021) 9:36 https://doi.org/10.1186/s40462-021-00275-5 RESEARCH Open Access Individual and seasonal variation in the movement behavior of two tropical nectarivorous birds Jennifer R. Smetzer1* , Kristina L. Paxton1 and Eben H. Paxton2 Abstract Background: Movement of animals directly affects individual fitness, yet fine spatial and temporal resolution movement behavior has been studied in relatively few small species, particularly in the tropics. Nectarivorous Hawaiian honeycreepers are believed to be highly mobile throughout the year, but their fine-scale movement patterns remain unknown. The movement behavior of these crucial pollinators has important implications for forest ecology, and for mortality from avian malaria (Plasmodium relictum), an introduced disease that does not occur in high-elevation forests where Hawaiian honeycreepers primarily breed. Methods: We used an automated radio telemetry network to track the movement of two Hawaiian honeycreeper species, the ʻapapane (Himatione sanguinea) and ʻiʻiwi (Drepanis coccinea). We collected high temporal and spatial resolution data across the annual cycle. We identified movement strategies using a multivariate analysis of movement metrics and assessed seasonal changes in movement behavior. Results: Both species exhibited multiple movement strategies including sedentary, central place foraging, commuting, and nomadism , and these movement strategies occurred simultaneously across the population. We observed a high degree of intraspecific variability at the individual and population level. The timing of the movement strategies corresponded well with regional bloom patterns of ‘ōhi‘a(Metrosideros polymorpha) the primary nectar source for the focal species. Birds made long-distance flights, including multi-day forays outside the tracking array, but exhibited a high degree of fidelity to a core use area, even in the non-breeding period. -
Keauhou Bird Conservation Center
KEAUHOU BIRD CONSERVATION CENTER Discovery Forest Restoration Project PO Box 2037 Kamuela, HI 96743 Tel +1 808 776 9900 Fax +1 808 776 9901 Responsible Forester: Nicholas Koch [email protected] +1 808 319 2372 (direct) Table of Contents 1. CLIENT AND PROPERTY INFORMATION .................................................................... 4 1.1. Client ................................................................................................................................................ 4 1.2. Consultant ....................................................................................................................................... 4 2. Executive Summary .................................................................................................. 5 3. Introduction ............................................................................................................. 6 3.1. Site description ............................................................................................................................... 6 3.1.1. Parcel and location .................................................................................................................. 6 3.1.2. Site History ................................................................................................................................ 6 3.2. Plant ecosystems ............................................................................................................................ 6 3.2.1. Hydrology ................................................................................................................................ -
From Jack Bean (Canavalia Ensiformis) Leaves
Plant Physiol. (1975) 55, 975-977 In Vitro Synthesis of Ureidohomoserine by an Enzyme from Jack Bean (Canavalia ensiformis) Leaves Received for publication December 9, 1974 and in revised form February 19, 1975 THOMAS DENNY O'NEAL Department of Biology, Rensselaer Polytechnic Institute, Troy, New York 12181 ABSTRACT Identification of the products employed the use of one- dimensional TLC on Silica Gel G An enzyme was extensively purified from jack bean leaves plates, using phenol-H2O (Canavalia (77:23, v/v) or secbutanol-16% NH,OH, (3:1, v/v) as the ensiformis L.) which produced o-ureidohomoserine solvents. Citrulline and from L-canaline and carbamyl phosphate. The most ureidohomoserine were located by highly puri- with or fied preparations catalyzed both this reaction and citrulline syn- spraying ninhydrin Ehrlich's reagent (2% w/v p-di- thesis from ornithine and and the ratio methylaminobenzaldehyde in 5% HCI). Both ureidohomo- carbamyl phosphate, of serine and the two activities remained nearly constant during purification. citrulline had approximately the same RF value When hydrated jack bean seeds were the in either solvent, and reacted with both reagents. enzyme source, orni- The thine carbamyltransferase (EC 2.1.3.3) activity was high but enzymes were assayed at 37 C for 10 min. The assay synthesis of ureidohomoserine was barely detectable. Both contained enzyme, 3 mM L-ornithine or L-canaline, 6 mM ornithine carbamyltransferase and the ureidohomoserine syn- carbamyl phosphate, 33 mm tris-HCl buffer, pH 7.8 (for thesizing enzyme had similar Km values for carbamyl phos- CCT' or pH 8.3 (for OCT) and H20 to a final volume of phate. -
Twenty-Three of 69 Since Discovery of 17 SOME LIMITING
17 SOME LIMITING FACTORS AND RESEARCH NEEDS OF ENDANGERED HAWAIIAN FOREST BIRDS Winston E. Banko U. S. Fish & Wildlife Service Hawaii Volcanoes National Park Hawaii 96718 It is well known that Hawaiian birds are particularly sus ceptible to depopulation and extinction. Twenty-three of 69 endemic species or races have disappeared since discovery of Hawai'i by Europeans 200 years ago. Except for Warner (1968) and Atkinson (1977), only super ficial inquiries have been made into historical aspects and underlying factors of the Hawaiian forest bird decline. After several years of field and laboratory investigation, Warner explained th~ rlisappearance of forest birds as being caused primarily by disease. Atkinson advanced a theory based on historical evidence that arboreal predation by rats was a leading factor. The object of my long-term historical investigation is to document and compare the salient facts on the geography and chro nology of Hawaiian bird loss, species by species; to chronicle what is known about all factors of depopulation~-predation, disease, habitat alteration, and food competition; and to draw such conclusions as seem warranted. At the First Conference in Natural Sciences two years ago, Banko and Banko (1976) reported on the potential significance of food depletion in the decline of Hawaiian forest birds. The role played by the Big-headed ant (Pheidole megacephala) in destroying much of the endemic insect fauna at elevations generally less than 3000 feet (914 m) before 1890 was sketched at that time. (The term "insect" will be used hereafter as including other arthropods as well). I now wish to elaborate on the possible impact of foreign parasitic flies and .wasps in depleting native insect foods impor tant to the small Hawaiian forest birds at higher elevation~. -
Ka Pilina Poina 'Ole Connections Not Forgotten Field Guide 2018
Ka Pilina Poina ‘Ole “Connections Not Forgotten” Species of the Dryland Forest Field Learning Guide Ka‘ūpūlehu Dryland Forest Preserve Kalaemanō Cultural Center La‘i‘Ōpua Dryland Preserve Pālamanui Dry Forest Preserve Endemic Mamane (Sophora chrysophylla) Botanical Names: Sophora chrysophylla, Edwardsia chrysophylla, Edwardsia unifoliata, Sophora grisea, Sophora lanaiensis, Sophora unifoliata Common Names: Mamane, Mamani Family: Fabaceae Potential or Traditional Uses: Lei (Flower or Seed), Wood Description: Mamane is a large shrub or medium sized‐tree up to 50 feet tall. The branches are golden brown with ridges running along them. Each leaf consists of 6 to 10 pairs of oval leaflets. The light green leaflets range in size from 3/8 to 2 inches long and 1/4 to 1 inch wide. The pea‐like yellow flowers form loose bunches at the bases of leaves or the ends of branches. Flowering occurs in winter and spring. Habitat and Geographic Range: Mamane is an endemic species found scattered throughout dry shrubland and dry to moist forests; it is also occasionally found in wet forests. It is the most common plant in the subalpine areas of East Maui and Hawai'i Island. It grows at elevations ranging from 1,400 to over 10,000 feet and is found on all the main Hawaiian islands except Ni'ihau and Kaho'olawe. Endangered, Endemic Uhiuhi (Caesalpinia kavaiensis) Botanical Names: Caesalpinia kavaiensis, Mezoneuron kavaiense Common Names: Uhiuhi, Kawa'u, Kea Family: Fabaceae Potential or Traditional Uses: Lei (Flower or Seed), Wood Description: Uhiuhi is a shrub or small tree ranging in height from 12 to over 30 feet.