HA Vol. 4 Layout For

Total Page:16

File Type:pdf, Size:1020Kb

HA Vol. 4 Layout For hawaiian archaeology 4 Volume 4, 1995 Society for Hawaiian Archaeology hawaiian archaeology Volume 4, 1995 Society for Hawaiian Archaeology Editor’s Note 3 Sara L. Collins Avifaunal Remains from the Kawailoa Site, O‘ahu Island (BPBM Site 50-OA-D6-62) 4 Frank R. Thomas Excavations at Maunalua Cave, Hawai‘i Kai, O‘ahu 17 Richard Pearson A Brief Report on Test Excavations at the Hawaiian Mission, Honolulu 27 Anne W. H. Garland An Archaeological Predictive Model for the Mission Houses Site in Honolulu and its Value 34 Matthew Spriggs Roadkill Archaeology on Läna‘i: A Historic House Site at Kahemano (State Site 1529) 45 Michael T. Pfeffer Distribution and Design of Pacific Octopus Lures: the Hawaiian Octopus Lure in Regional Context 47 hawaiian archaeology 4 Melinda S. Allen, Editor Production of this volume was made possible with the generous financial assistance of: Robert E. Black Memorial Fund B. P. Bishop Museum Archaeology, Inc. Paul H. Rosendahl, Ph.D., Inc. – Editor‘s Note This volume marks an important point in the history of Hawaiian Archaeology, as the Society brings to publication the last of its outstanding papers from the late 1980s. Volumes 2, 3, and 4 are witnesses to the commitment of our membership and board to producing a professional and timely journal. I am appreciative of the willingness of Anne Garland, Richard Pearson, Matthew Spriggs, and Frank Thomas to work with me on editorial details, despite the many years between submission and publication. The papers of Volume 4 reflect three trends in Hawaiian Archaeology. The paper by Collins is an exam- ple of the increasing interest in re-examining previously collected materials, while Thomas synthesizes information from a second previously excavated but poorly known site. Collins takes a fresh look at the avifauna from Kawailoa, O‘ahu, comparing them with finds from other archaeological and paleontolog- ical sites in the region. Notably, this is the first published account of this relatively early occupation site and Collins also summarizes important information on the radiocarbon sequence and non-bird fauna. Likewise, Thomas’ paper makes available stratigraphic, radiocarbon, and artifact data from Maunalua Cave, an important leeward O‘ahu site. Other studies of previously excavated materials are currently underway by University of Hawai‘i and Bishop Museum research teams. Like the contribution of Collins, these efforts underscore both the potential of these older collections to provide new information and the importance of carefully documenting and managing archaeological resources for future studies. The papers by Pearson, Garland, and Spriggs register an early, and recently accelerated, interest in his- torical archaeology, the period of Hawaiian history after A.D. 1778. The importance historical archaeolo- gy has assumed locally is also indicated by the enthusiastic response to the workshop and symposium organized by Susan Lebo for the 7th Annual Hawaiian Archaeology Conference. Finally, the paper by Michael Pfeffer, along with recent literature elsewhere, signals renewed interest in traditional material culture studies. Departing from earlier research, Pfeffer examines not only historical aspects of artifact form and distribution related to culture-contact but also functional features of mor- phology which relate to environmental conditions. He offers a regional perspective on the ingenious Pacific octopus lure, and suggests that important design changes in this tool may have occurred in the Hawaiian Islands. M.S.A. 3 Avifaunal Remains from the Kawailoa Site, O‘ahu Island (BPBM Site 50-OA-D6-62) Sara L. Collins State of Hawai‘i Historic Preservation Division A major theme of Pacific prehistory has centered on human agency in the disap- pearance of endemic bird species which once flourished on nearly all of the arch- ipelagos of Oceania. From the smallest and most remote islands, like Tikopia or Henderson (Steadman and Olson 1985; Steadman et al. 1990; Weisler et al. 1991), to the largest island archipelagos of Hawai‘i and New Zealand (Anderson 1989; Olson and James 1984), a growing number of studies have demonstrated the link between human settlement and the extinction or extirpation of avifauna. In the Hawaiian Islands, inferences drawn from research on avifaunal remains from paleontological sites have shaped thinking about the nature of human/bird relationships (Olson and James 1982, 1991). According to these views, the impact of the original Polynesian colonists was immediate and devastating, with the majority of extinctions taking place in the pre-Contact1 era (Olson and James 1984). To a lesser extent, excavations of archaeological sites in Hawai‘i have informed research on avian extinctions by providing additional data on presumed prey species of the Polynesians found in midden and, in some instances, radio- carbon dates of such deposits (James et al. 1987; Schilt 1984). It would seem that avifaunal remains from firmly dated archaeological sites would potentially yield the most significant and detailed information on the scope and pace of bird extinctions and extirpations in Hawai‘i. The goal of this paper is to refine our understanding of human/bird interactions in Hawai‘i by an examination of archaeological data obtained from several pre-Contact habitation sites in the Hawaiian Islands (Fig. 1). 4 5 collins Materials and Methods Field Methods and Preliminary Results In 1984, Bishop Museum Anthropology staff con- ducted excavations at site 50-Oa-D6-62, a habita- tion site at Kawailoa on the north shore of O‘ahu Island (Garland n.d., 1984a, 1984b), as shown in Fig- ure 1. Associated with a nearby fishing shrine or ko‘a, Site D6-62 covered an area of approximately 1,152 m2 and had a number of activity areas and unex- pectedly rich and extensive pre-Contact deposits. Features identified at Site D6-62 included a proba- ble cooking area, postmolds, refuse pits, and four human burials (Fig. 2). All excavated deposits were screened through 1/4 in and 1/8 in mesh, with each fraction bagged separately. Figure 1. Map of the Hawaiian Islands, showing location of Kawailoa Site and other archaeological The relatively complex sequence of occupations at localities discussed in text. the Kawailoa Site is represented by the two major cultural layers (called here Layer I and Layer Ib) and the numerous features identified during the excava- tion. The radiocarbon and volcanic glass age deter- minations obtained from fieldwork at Site D6-62 indicate considerable pre-Contact use of the site. As can be seen in Table 1, there appears to be an earlier component to the site, dating to between .. 1280 and 1460, and a later component, which extends from the seventeenth century .. into perhaps the early post-Contact era (circa .. 1800). The vol- canic glass age determinations, as seen in Table 2, corroborate the 14C age determinations, but provide a somewhat more continuous chronology, ranging from .. 1344 to 1674. Laboratory Methods Laboratory sorting and analysis of midden primarily focused on the feature contents, with the 1/4 in fau- nal bone sampled much more extensively than the 1/8 in fractions, although selected 1/8 in materials were examined. The 1/4 in faunal remains from the southeast quadrants of grid units BB10, CC9, and DD8 were also analyzed. It is estimated that approx- imately 5 to 10 % (by weight) of the total bone mid- den recovered from the Kawailoa Site has been examined to date. The results of bone midden analy- Figure 2. Base map of south parcel (TMK: 6-1-3:26), sis were originally recorded as weights in order to showing locations of archaeological sites and test compare findings with the results of shell midden excavations (from Athens and Shun 1982). analysis in which the shell is usually weighed. For 6 hawaiian archaeology Table 1 Radiocarbon Age Determinations from Site 50-Oa-D6-62 Results of Analyses Kawailoa, O‘ahu, Hawaiian Islands BPBM Provenience 14C Ages in Years Calibrated Range in HRC NO. .. ± 1 Sigmaa Years ..b (2 Sigma) Taxonomic Diversity Table 3 contains a list of the vertebrate faunal taxa HRC 392 T.P. 1/Layer 1 <150 .. <.. 1684 identified from the Kawailoa Site deposits, together HRC 393 T.P. 2/Layer 1 <370 .. <.. 1475 with the common names of the taxa, and Table 4 HRC 811 BB10/ Fe. 1 <170 .. <.. 1678 contains the total NISPs and MNIs for all taxa. In (hearth) general, nearly all vertebrate faunal bones could at least be assigned to zoological class; less than 1% of HRC 812 BB10/ Fe. 4 <180 .. <.. 1675 (postmold) the bone fragments were identified as “Medium Vertebrate,” which could represent bone from a fish, HRC 813 DD7/ Fe. 3 580 ± 80 .. .. 1280–1460 bird, or mammal. Similarly, less than 1% of the (oven) bone midden was probably derived from cartilagi- HRC 814 CC9/ Fe. 1 <150 .. <.. 1684 nous fishes (Sharks and Rays). Bony fish remains (firepit) formed the single largest component of the Kawailoa .. .. HRC 815 CC9/ Fe. 2 150 ± 80 1600–1955 vertebrate faunal midden—83%—while mam- (hearth) malian remains composed about 15% of the total. .. .. HRC 816 CC9/ Fe. 4 600 ± 80 1280–1450 Finally, nearly 2% of the bone was derived from (postmold) avian taxa. Table 5 presents some of these compara- HRC 817 CC9/ Fe. 5 140 ± 90 .. .. 1640–1955 tive statistics. (ash deposit) HRC 818 CC9/ Layer Ib 110 ± 80 .. .. 1670–1955 The NISPs for each zoological class of faunal remains can also be used as measures of diversity. While more HRC 819 DD8/ Fe. 4 210 ± 60 .. .. 1630–1890 (oven) than 6,700 fish bones were identified from these deposits, only about 3% were identified beyond the HRC 820 DD8/ Layer Ia <190 .. <.. 1672 level of class—to family, genus, or species. Approxi- a Dates given are uncalibrated, 13C-adjusted 14C ages (i.e., conventional radiocarbon mately 25% of the avifaunal remains were identified ages).
Recommended publications
  • Convergent Evolution of 'Creepers' in the Hawaiian Honeycreeper
    ARTICLE IN PRESS Biol. Lett. 1. INTRODUCTION doi:10.1098/rsbl.2008.0589 Adaptive radiation is a fascinating evolutionary pro- 1 cess that has generated much biodiversity. Although 65 2 Evolutionary biology several mechanisms may be responsible for such 66 3 diversification, the ‘ecological theory’ holds that it is 67 4 the outcome of divergent natural selection between 68 5 Convergent evolution of environments (Schluter 2000). Whether adaptive 69 6 radiations result chiefly from such ecological speciation, 70 7 ‘creepers’ in the Hawaiian however, remains unclear (Schluter 2001). Convergent 71 8 evolution is often considered powerful evidence for the 72 9 honeycreeper radiation role of adaptive forces in the speciation process 73 (Futuyma 1998), and thus documenting cases where it 10 Dawn M. Reding1,2,*, Jeffrey T. Foster1,3, 74 has occurred is important in understanding the link 11 Helen F. James4, H. Douglas Pratt5 75 12 between natural selection and adaptive radiation. 76 and Robert C. Fleischer1 13 The more than 50 species of Hawaiian honeycree- 77 1 14 Center for Conservation and Evolutionary Genetics, National pers (subfamily Drepanidinae) are a spectacular 78 Zoological Park and National Museum of Natural History, 15 Smithsonian Institution, Washington, DC 20008, USA example of adaptive radiation and an interesting 79 16 2Department of Zoology, University of Hawaii, Honolulu, system to test for convergence, which has been 80 17 HI 96822, USA suspected among the nuthatch-like ‘creeper’ eco- 81 3Center for Microbial Genetics & Genomics,
    [Show full text]
  • The Relationships of the Hawaiian Honeycreepers (Drepaninini) As Indicated by Dna-Dna Hybridization
    THE RELATIONSHIPS OF THE HAWAIIAN HONEYCREEPERS (DREPANININI) AS INDICATED BY DNA-DNA HYBRIDIZATION CH^RrES G. SIBLEY AND Jo• E. AHLQUIST Departmentof Biologyand PeabodyMuseum of Natural History, Yale University, New Haven, Connecticut 06511 USA ABSTRACT.--Twenty-twospecies of Hawaiian honeycreepers(Fringillidae: Carduelinae: Drepaninini) are known. Their relationshipsto other groups of passefineswere examined by comparing the single-copyDNA sequencesof the Apapane (Himationesanguinea) with those of 5 speciesof carduelinefinches, 1 speciesof Fringilla, 15 speciesof New World nine- primaried oscines(Cardinalini, Emberizini, Thraupini, Parulini, Icterini), and members of 6 other families of oscines(Turdidae, Monarchidae, Dicaeidae, Sylviidae, Vireonidae, Cor- vidae). The DNA-DNA hybridization data support other evidence indicating that the Hawaiian honeycreepersshared a more recent common ancestorwith the cardue!ine finches than with any of the other groupsstudied and indicate that this divergenceoccurred in the mid-Miocene, 15-20 million yr ago. The colonizationof the Hawaiian Islandsby the ancestralspecies that radiated to produce the Hawaiian honeycreeperscould have occurredat any time between 20 and 5 million yr ago. Becausethe honeycreeperscaptured so many ecologicalniches, however, it seemslikely that their ancestor was the first passefine to become established in the islands and that it arrived there at the time of, or soon after, its separationfrom the carduelinelineage. If so, this colonist arrived before the present islands from Hawaii to French Frigate Shoal were formed by the volcanic"hot-spot" now under the island of Hawaii. Therefore,the ancestral drepaninine may have colonizedone or more of the older Hawaiian Islandsand/or Emperor Seamounts,which also were formed over the "hot-spot" and which reachedtheir present positions as the result of tectonic crustal movement.
    [Show full text]
  • 25 Using Community Group Monitoring Data to Measure The
    25 Using Community Group Monitoring Data To Measure The Effectiveness Of Restoration Actions For Australia's Woodland Birds Michelle Gibson1, Jessica Walsh1,2, Nicki Taws5, Martine Maron1 1Centre for Biodiversity and Conservation Science, School of Earth and Environmental Sciences, University of Queensland, St Lucia, Brisbane, 4072, Queensland, Australia, 2School of Biological Sciences, Monash University, Clayton, Melbourne, 3800, Victoria, Australia, 3Greening Australia, Aranda, Canberra, 2614 Australian Capital Territory, Australia, 4BirdLife Australia, Carlton, Melbourne, 3053, Victoria, Australia, 5Greening Australia, PO Box 538 Jamison Centre, Macquarie, Australian Capital Territory 2614, Australia Before conservation actions are implemented, they should be evaluated for their effectiveness to ensure the best possible outcomes. However, many conservation actions are not implemented under an experimental framework, making it difficult to measure their effectiveness. Ecological monitoring datasets provide useful opportunities for measuring the effect of conservation actions and a baseline upon which adaptive management can be built. We measure the effect of conservation actions on Australian woodland ecosystems using two community group-led bird monitoring datasets. Australia’s temperate woodlands have been largely cleared for agricultural production and their bird communities are in decline. To reverse these declines, a suite of conservation actions has been implemented by government and non- government agencies, and private landholders. We analysed the response of total woodland bird abundance, species richness, and community condition, to two widely-used actions — grazing exclusion and replanting. We recorded 139 species from 134 sites and 1,389 surveys over a 20-year period. Grazing exclusion and replanting combined had strong positive effects on all three bird community metrics over time relative to control sites, where no actions had occurred.
    [Show full text]
  • Appendix, French Names, Supplement
    685 APPENDIX Part 1. Speciesreported from the A.O.U. Check-list area with insufficient evidencefor placementon the main list. Specieson this list havebeen reported (published) as occurring in the geographicarea coveredby this Check-list.However, their occurrenceis considered hypotheticalfor one of more of the following reasons: 1. Physicalevidence for their presence(e.g., specimen,photograph, video-tape, audio- recording)is lacking,of disputedorigin, or unknown.See the Prefacefor furtherdiscussion. 2. The naturaloccurrence (unrestrained by humans)of the speciesis disputed. 3. An introducedpopulation has failed to becomeestablished. 4. Inclusionin previouseditions of the Check-listwas basedexclusively on recordsfrom Greenland, which is now outside the A.O.U. Check-list area. Phoebastria irrorata (Salvin). Waved Albatross. Diornedeairrorata Salvin, 1883, Proc. Zool. Soc. London, p. 430. (Callao Bay, Peru.) This speciesbreeds on Hood Island in the Galapagosand on Isla de la Plata off Ecuador, and rangesat seaalong the coastsof Ecuadorand Peru. A specimenwas takenjust outside the North American area at Octavia Rocks, Colombia, near the Panama-Colombiaboundary (8 March 1941, R. C. Murphy). There are sight reportsfrom Panama,west of Pitias Bay, Dari6n, 26 February1941 (Ridgely 1976), and southwestof the Pearl Islands,27 September 1964. Also known as GalapagosAlbatross. ThalassarchechrysosWma (Forster). Gray-headed Albatross. Diornedeachrysostorna J. R. Forster,1785, M6m. Math. Phys. Acad. Sci. Paris 10: 571, pl. 14. (voisinagedu cerclepolaire antarctique & dansl'Ocean Pacifique= Isla de los Estados[= StatenIsland], off Tierra del Fuego.) This speciesbreeds on islandsoff CapeHorn, in the SouthAtlantic, in the southernIndian Ocean,and off New Zealand.Reports from Oregon(mouth of the ColumbiaRiver), California (coastnear Golden Gate), and Panama(Bay of Chiriqu0 are unsatisfactory(see A.O.U.
    [Show full text]
  • Description of Adults, Eggshells, Nestling, Fledgling, and Nest of the Poo-Uli
    THE WILSON BULLETIN A QUARTERLY MAGAZINE OF ORNITHOLOGY Published by the Wilson Ornithological Society VOL. 108, No. 4 DECEMBER 1996 PAGES 607-848 Wilson Bull., 108(4), 1996, pp. 607-619 DESCRIPTION OF ADULTS, EGGSHELLS, NESTLING, FLEDGLING, AND NEST OF THE POO-ULI ANDREW ENGILIS, JR., ’ THANE K. PRATT,* CAMERON B. KEPLER,~ A. MARIE ECTON,~ AND KIMBERLY M. FLUETSCH~ ABSTRACT.-The Poo-uli (Melamprosops phaeosoma), a Hawaiian honeycreeperdiscov- ered on the island of Maui in 1973 and now near extinction,is representedin museums by only two specimens. Based on the first observations of a nesting pair and re-examination of the two specimens, we describe the adult male and female, eggshells, nestling, and fledgling Poo-uli. Poo-uli are sexually monochromatic but males are brighter. The male is brown above, whitish below, and has an extensive black mask bordered with gray on the crown and a distinct white auricular patch. The female differs in having a similar facial pattern not as sharply demarked and in having a grayish wash below. The observed fledgling resembled the adults but was paler brown above and whitish below and had a much smaller black mask and pale mandible. We tentatively assigned both museum specimens to first basic plumage because they resembled the adult female but retained some pale juvenal coloration in the mandible. We also determined from dissection that the holotype was an immature male; we could not determine sex of the paratype. The nest was an open cup of twigs and bryophytes with a thin lining of fern rootlets. The nest contained eggshell frag- ments with brown-gray speckling against a whitish background.
    [Show full text]
  • Revised Recovery Plan for Hawaiian Forest Birds 2-1
    II. SPECIES ACCOUNTS Section II contains accounts of all species covered in this recovery plan, presented in taxonomic order following the American Ornithologists’ Union checklist (1998). These accounts are not meant to be a complete reference, but rather to summarize sufficient relevant information about each species in order to understand the prescribed recovery strategy and the prioritization of recovery actions. All of the Hawaiian forest birds face the same set of threats, but the relative importance of those threats varies among species depending on their life history, current distribution and status, and habitat requirements. The priority placed on each component of the recovery strategy therefore varies among species. The species accounts build on and refine the overall recovery strategy discussed in the Introduction (Section I), and justify the recovery criteria presented in Section III as well as the recovery actions and priorities presented in the Recovery Actions Narrative (Section IV). Each account also includes a summary of previous and ongoing conservation efforts, including Federal and State regulations, land acquisition, research, and management directed at or relevant to the recovery of the species. All of the accounts follow the same format and contain the following section headings: description and taxonomy; life history; habitat description; historical and current range and status; reasons for decline and current threats; conservation efforts; and recovery strategy. Longer accounts for better-studied species contain additional subheadings to help locate information. When available, maps showing the historical and current distribution of the species and recovery areas appear in the accounts (Figures 6 through 21). Recovery plans are prepared following a determination that a species merits listing as endangered or threatened under the Endangered Species Act (Act).
    [Show full text]
  • Clade-Specific Morphological Diversification and Adaptive
    Received 14 February 2001 FirstCite Accepted 21 June 2001 e-publishing Published online Date Clade-specific morphological diversification and adaptive radiation in Hawaiian songbirds Irby J. Lovette1,2*, Eldredge Bermingham2 and Robert E. Ricklefs3 1Cornell Laboratory of Ornithology and Department of Ecology and Evolutionary Biology, Cornell University, 159 Sapsucker Woods Road, Ithaca, NY 14850, USA 2Smithsonian Tropical Research Institute, PO Box 2072, Balboa, Panama 3Department of Biology, University of Missouri-St Louis, 8001 Natural Bridge Road, St Louis, MO 63121, USA The Hawaiian honeycreepers are a dramatic example of adaptive radiation but contrast with the four other songbird lineages that successfully colonized the Hawaiian archipelago and failed to undergo similar diversification. To explore the processes that produced the diversity dichotomy in this insular fauna, we compared clade age and morphological diversity between the speciose honeycreepers and the compara- tively depauperate Hawaiian thrushes. Mitochondrial-DNA-based genetic distances between these Hawai- ian clades and their continental sister taxa indicate that the ancestral thrush colonized the Hawaiian Islands as early as the common ancestor of the honeycreepers. This similar timing of colonization indicates that the marked difference in diversity between the Hawaiian honeycreeper and thrush clades is unlikely to result from differences in these clades’ tenures within the archipelago. If time cannot explain the con- trasting diversities of these taxa, then an intrinsic, clade-specific trait may have fostered the honeycreeper radiation. As the honeycreepers have diversified most dramatically in morphological characters related to resource utilization, we used principal components analyses of bill characters to compare the magnitudes of morphological variation in the ancestral clades from which the Hawaiian honeycreeper and thrush lineages are derived, the Carduelini and Turdinae respectively.
    [Show full text]
  • Palila (Loxioides Bailleui)
    Hawaiian Bird Conservation Action Plan Focal Species: Palila (Loxioides bailleui) Synopsis: The Palila is a specialized Hawaiian honeycreeper with a population of only 1,263 birds that are restricted to 45 km2 of remnant high elevation māmane forest on Mauna Kea. Palila numbers have declined annually since 2003 because of long-term drought and habitat degradation by feral sheep introduced for hunting. Lawsuits resulted in Federal court orders in 1979, 1987, and 1998 that mandated removal of feral ungulates from Palila Critical Habitat, but a substantial number of feral sheep remain. Following a settlement agreement in 2009, fencing efforts are underway and sheep eradication is expected to follow, but natural forest regeneration and active restoration will take time. Greater public and local government support are needed. Māmane forest, Mauna Kea. Photo David Leonard. Adult male Palila. Photo Eric VanderWerf. Population Size and Trend: Range-wide Geographic region: Hawaiian Islands population surveys have been conducted annually Group: Forest Birds since 1980 (Johnson et al. 2006, Leonard et al. Federal Status: Endangered 2008, Banko et al. in press). Population estimates State status: Endangered fluctuated between 2,000 and 7,000 birds from IUCN status: Critically endangered 1980 to 2004, but no statistically significant Conservation score, rank: 20/20, At-risk trends were detected (Johnson et al. 2006). Watch List 2007 Score: Red However, Leonard et al. (2008) documented a Climate Change Vulnerability: High significant decline beginning in 2003 that has continued through 2011. From 2003 to 2011, population estimates declined each year by an average of 586 ± 106 birds for a mean annual loss of 17% ± 3.5 or 79% overall (Banko et al.
    [Show full text]
  • A Systematic Analysis of the Endemic Avifauna of the Hawaiian Islands. Harold Douglas Pratt Rj Louisiana State University and Agricultural & Mechanical College
    Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1979 A Systematic Analysis of the Endemic Avifauna of the Hawaiian Islands. Harold Douglas Pratt rJ Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Pratt, Harold Douglas Jr, "A Systematic Analysis of the Endemic Avifauna of the Hawaiian Islands." (1979). LSU Historical Dissertations and Theses. 3347. https://digitalcommons.lsu.edu/gradschool_disstheses/3347 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. INFORMATION TO USERS This was produced from a copy of a document sent to us for microfilming. While the most advanced technological means to photograph and reproduce this document have been used, the quality is heavily dependent upon the quality of the material submitted. The following explanation of techniques is provided to help you understand markings or notations which may appear on this reproduction. 1. The sign or “target” for pages apparently lacking from the document photographed is “Missing Page(s)”. If it was possible to obtain the missing page(s) or section, they are spliced into the film along with adjacent pages. This may have necessitated cutting through an image and duplicating adjacent pages to assure you of complete continuity. 2. When an image on the film is obliterated with a round black mark it is an indication that the Him inspector noticed either blurred copy because of movement during exposure, or duplicate copy.
    [Show full text]
  • Iwi (Vestiaria Coccinea) As Threatened Or Endangered Under the U.S
    PETITION TO LIST THE `I`IWI (VESTIARIA COCCINEA) AS THREATENED OR ENDANGERED UNDER THE U.S. ENDANGERED SPECIES ACT August 24, 2010 Center for Biological Diversity `I`IWI (VESTIARIA COCCINEA) Photo source: Wikipedia 1 August 24, 2010 Ken Salazar, Secretary of the Interior Robyn Thorson, Regional Director U.S. Department of the Interior U.S. Fish & Wildlife Service 1849 C Street N.W. Pacific Region Washington, DC 20240 911 NE 11th Ave Portland, Oregon 97232 Dear Secretary Salazar, The Center for Biological Diversity, Noah Greenwald, and Dr. Tony Povilitis formally petition to list the `I`iwi (Vestiaria coccinea) as a threatened or endangered species pursuant to the Endangered Species Act (ESA), 16 U.S.C. §1531 et seq. This petition is filed under 5 U.S.C. 553(e) and 50 CFR 424.14 (1990), which grant interested parties the right to petition for issuance of a rule from the Secretary of Interior. Under the ESA, a threatened species includes “any species which is likely to become an endangered species within the foreseeable future throughout all or a signification portion of its range.” An “endangered species” is one that is in danger of extinction. The `I`iwi warrants listing because it is imperiled by climate change and disease in combination with other factors, is declining in population size and range, and is not adequately protected by existing regulatory mechanisms. With climate change forcing the spread of avian malaria and avian pox, the `I`iwi is in danger of near term extinction in the western portion of its range (the islands of Kauai, Oahu, and Molokai, and on west Maui), and severe population declines with risk of extinction within the foreseeable future across its eastern range (east Maui and the island of Hawaii).
    [Show full text]
  • Draft Revised Recovery Plan for Hawaiian Forest Birds
    DRAFT REVISED RECOVERY PLAN FOR HAWAIIAN FOREST BIRDS August 2003 Original plans completed: February 3, 1983 (Hawaii Forest Birds) July 29, 1983 (Kauai Forest Birds) May 30, 1984 (Maui-Molokai Forest Birds) June 27, 1986 (Palila) Region 1 U.S. Fish and Wildlife Service Portland, Oregon Approved: _____________________________________________ Regional Director, U.S. Fish and Wildlife Service Date: _____________________________________________ Dedication To the naturalists and scientists of Hawai`i who have contributed to our understanding of the biology and ecology of Hawaiian forest birds. ii GUIDE TO RECOVERY PLAN ORGANIZATION This recovery plan provides individual species accounts and actions needed Statewide for recovery of 21 taxa of forest birds in Hawai`i. The plan covers a group of species for which the threats and limiting factors are similar, and for which similar actions are needed for recovery. Many of the recovery actions are needed throughout all recovery habitat for each species. In other cases the plan identifies specific land parcels where a particular recovery action is needed. Section I, the Introduction, provides an overview of the causes for decline of Hawaiian forest birds and the current threats, ongoing conservation efforts, and general recovery strategies for the species covered by this plan. The Species Accounts in Section II summarize information on taxonomy, life history, habitat requirements, current and historical ranges, population status, reasons for decline and current threats, and species-specific conservation efforts and recovery strategies. Section III, Recovery, presents recovery objectives and criteria for each species, maps of recovery habitat on each of the main Hawaiian Islands where they occur, criteria used to delineate the recovery habitat boundaries, and a description of the steps to be taken in the event that an individual of one of the extremely rare species is located.
    [Show full text]
  • (Family Drepanididae) Have Received C
    J. Yamashina Inst. Ornith., 14: 81-85, 1982 Pterylosis of Some Hawaiian Honeycreepers, Drepanididae Andrew J. Berger* Abstract This paper describes and illustrates the feather tracts in three species of Hawaiian Honeycreepers: Nihoa Finch, Amakihi, and Apapane. The author believes, with others , that the ancestor for the honeycreepers was a cardueline finch, and that this ancestor probably reached the Hawaiian Islands from Asia, and not from North or Central America. Honeycreeper Feather Tracts The endemic Hawaiian honeycreepers (family Drepanididae) have received con- siderable attention during the past decade (Eddinger 1970, Sibley 1970, Richards & Bock 1973, Raikow 1976, van Riper 1980, Berger 1981, Sibley & Ahlquist 1982). However, very little has been published about the pterylosis of this family. Gadow (1890-1899) discussed briefly and illustrated portions of the feather tracts of several species: Palila (Loxiodes bailleui), Kauai Akialoa (Hemignathus procerus), and Kauai Creeper (Oreomystis bairdi). Van Tyne & Berger (1976: 133) illustrated the dorsal feather tracts of the Apapane (Himatione sanguinea). In this paper I present figures of the dorsal and ventral feather tracts of three honeycreepers that Pratt (1979) and Berger (1981) placed in three tribes or subfamilies of this group: Nihoa Finch (Telespyza ultima; subfamily Psittirostrinae), Hawaii Amakihi (Hemignathus virens; subfamily Hemignathinae), and Apapane (Himatione sanguinea, subfamily Drepanidinae). Alar tract. There are nine secondaries, the innermost being the smallest and shortest (Figures 1A, B, C). There are nine functional primaries; the tenth primary is rudimentary and is called a remicle. In the Amakihi, for example, the tenth primary is only 5mm in length, whereas the ninth primary is 47mm long; in one specimen of the extinct Hawaii Akialoa (Hemignathus o.
    [Show full text]