<?xml version="1.0" encoding="UTF-8"?>
<rss xmlns:dc="http://purl.org/dc/elements/1.1/" version="2.0">
<channel>
<title>Pacific Science, Volume 33, Numbers 1-4, 1979</title>
<link>http://hdl.handle.net/10125/1046</link>
<description/>
<pubDate>Thu, 23 May 2013 05:53:14 GMT</pubDate>
<dc:date>2013-05-23T05:53:14Z</dc:date>
<image>
<title>Pacific Science, Volume 33, Numbers 1-4, 1979</title>
<url>http://scholarspace.manoa.hawaii.edu:80/bitstream/id/2930/PacSci.jpg</url>
<link>http://hdl.handle.net/10125/1046</link>
</image>
<item>
<title>33: Index - Pacific Science</title>
<link>http://hdl.handle.net/10125/1496</link>
<pubDate>Mon, 01 Jan 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1496</guid>
<dc:date>1979-01-01T00:00:00Z</dc:date>
</item>
<item>
<title>Harold St. John -- Career Synopsis and Bibliography</title>
<link>http://hdl.handle.net/10125/1495</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1495</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
</item>
<item>
<title>Revision of the Genus Pandanus Stickman. Part 43 Pandanus in Tahiti</title>
<link>http://hdl.handle.net/10125/1494</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1494</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
<dc:creator>St. John, Harold</dc:creator>
</item>
<item>
<title>Revision of the Genus Pandanus Stickman. Part 42 Pandanus tectorius Parkins. ex Z and Pandanus odoratissimus L.f.</title>
<link>http://hdl.handle.net/10125/1493</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1493</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
<dc:creator>St. John, Harold</dc:creator>
</item>
<item>
<title>Cyrtandra (Gesneriaceae) from Kauai and Maui. Hawaiian Plant Studies 96</title>
<link>http://hdl.handle.net/10125/1492</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1492</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
<dc:creator>St. John, Harold</dc:creator>
</item>
<item>
<title>A Variety of Colubrina oppositifolia Brongn. ex Mann (Rhamnaceae). Hawaiian Plant Studies 95</title>
<link>http://hdl.handle.net/10125/1491</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1491</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
<dc:creator>St. John, Harold</dc:creator>
</item>
<item>
<title>The Native Hawaiian Species of Morinda (Rubiaceae). Hawaiian Plant Studies 94</title>
<link>http://hdl.handle.net/10125/1490</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1490</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
<dc:creator>St. John, Harold</dc:creator>
</item>
<item>
<title>Classification of Acacia Koa and Relatives (Leguminosae). Hawaiian Plant Studies 93</title>
<link>http://hdl.handle.net/10125/1489</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1489</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
<dc:creator>St. John, Harold</dc:creator>
</item>
<item>
<title>New Species of Cyrtandra (Gesneriaceae) from Kauai. Hawaiian Plant Studies 74</title>
<link>http://hdl.handle.net/10125/1488</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1488</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
<dc:creator>St. John, Harold</dc:creator>
</item>
<item>
<title>Monograph of the Hawaiian Species of Achyranthes (Amaranthaceae). Hawaiian Plant Studies 56</title>
<link>http://hdl.handle.net/10125/1487</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1487</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
<dc:creator>St. John, Harold</dc:creator>
</item>
<item>
<title>The Native Species of Senecio (Compositae) in Hawaii Hawaiian Plant Studies 53</title>
<link>http://hdl.handle.net/10125/1486</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1486</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
<dc:creator>St. John, Harold</dc:creator>
</item>
<item>
<title>The Botany of Niihau Island, Hawaii, as Seen on Captian Cook's Voyage, 1778-1779</title>
<link>http://hdl.handle.net/10125/1485</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1485</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
<dc:creator>St. John, Harold</dc:creator>
</item>
<item>
<title>The Botany of Kauai Island, Hawaii, as Seen on Captain Cook's Voyage, 1778</title>
<link>http://hdl.handle.net/10125/1484</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1484</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
<dc:creator>St. John, Harold</dc:creator>
</item>
<item>
<title>33:4 Table of Contents - Pacific Science</title>
<link>http://hdl.handle.net/10125/1483</link>
<pubDate>Mon, 01 Oct 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1483</guid>
<dc:date>1979-10-01T00:00:00Z</dc:date>
</item>
<item>
<title>Penaeid Prawns in Fanga uta Lagoon, Tongatapu</title>
<link>http://hdl.handle.net/10125/1482</link>
<description>The penaeid prawns Penaeus semisulcatus and Metapenaeus&#13;
ensis were surveyed in Fanga'uta Lagoon, Tongatapu, between July 1975 and&#13;
August 1976. Catch rates indicate maximum abundance of P. semisulcatus&#13;
from September to November and minimum abundance between January&#13;
and February. Juveniles were found in March. Maximum abundance of M.&#13;
ensis occurred from mid-October to January and minimum abundance from&#13;
mid-February to mid-April. Spawning occurred outside the lagoon between&#13;
January and March, and juveniles were found in the lagoon in late April. All&#13;
areas of the lagoon show a similar pattern of catch rates. Catch rates of&#13;
prawns were reduced by one-third during the light phase of the moon, and the&#13;
full moon appears to be a factor associated with moulting in M. ensis.
</description>
<pubDate>Sun, 01 Jul 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1482</guid>
<dc:date>1979-07-01T00:00:00Z</dc:date>
<dc:creator>Braley, Richard D</dc:creator>
</item>
<item>
<title>A New Stenopodidean Shrimp (Decapoda, Natantia) from the Chatham Rise, New Zealand</title>
<link>http://hdl.handle.net/10125/1481</link>
<description>A new stenopodidean shrimp, Spongicoloides novaezelandiae sp.&#13;
nov., taken in a depth of about 1000 m in the Chatham Rise is described and&#13;
illustrated. It is somewhat similar to the east Atlantic Spongicoloides evolutus&#13;
(Bouvier), from which it is readily distinguished by the number of gills on the&#13;
maxillipeds. The genus Spongicoloides Hansen, previously known only from&#13;
the Atlantic, is recorded for the first time from New Zealand waters as well as&#13;
from the Pacific.
</description>
<pubDate>Sun, 01 Jul 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1481</guid>
<dc:date>1979-07-01T00:00:00Z</dc:date>
<dc:creator>Baba, Keiji</dc:creator>
</item>
<item>
<title>A Biological Determination of the Taxonomic Status of Conus elisae Kiener in Hawaii</title>
<link>http://hdl.handle.net/10125/1480</link>
<description>A population of Conus pennaceus Born was examined at&#13;
Hauula, Oahu, and was found to include darkly pigmented specimens referable&#13;
to C. elisae Kiener. The larvae from an egg mass laid by one of the&#13;
darkly pigmented cones were reared in the laboratory. Of seven surviving&#13;
larvae, six developed the C. pennaceus color pattern, while one developed the.&#13;
C. elisae pattern. It was concluded that Hawaiian cone shells which have in the&#13;
past been referred to C. elisae are simply rare color forms of C. pennaceus.
</description>
<pubDate>Sun, 01 Jul 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1480</guid>
<dc:date>1979-07-01T00:00:00Z</dc:date>
<dc:creator>Perron, Frank E</dc:creator>
</item>
<item>
<title>The Biology of Hastula inconstans (Hinds, 1844) and a Discussion of Life History Similarities among other Hastulas of Similar Proboscis Type</title>
<link>http://hdl.handle.net/10125/1479</link>
<description>Terebrid gastropods of the genus Hastula are found in great&#13;
abundance on fine-sand beaches throughout the tropics. Hastula inconstans, a&#13;
species common to surf beaches in the Hawaiian Islands, is the first hastula for&#13;
which a complete life history is known. Hastula inconstans is a primary&#13;
carnivore, preying exclusively on Dispio magna, a tube-dwelling, depositfeeding&#13;
spionid polychaete. The gastropod lives just beyond the surf zone and&#13;
exhibits well-developed adaptations that permit survival in this habitat. The&#13;
broad, fleshy foot, used in anchoring the snail in the sand and in rapid reburrowing,&#13;
is also highly modified as a "sail" which carries H. inconstans up&#13;
and down the beach with the passage of waves. A highly specialized foregut&#13;
contains long retractile labial and buccal tubes, which, combined with a poison&#13;
bulb and radular teeth, rapidly sting, immobilize, and ingest prey. The snail&#13;
lies buried in the sand when not feeding, but emerges when prey are detected&#13;
by distance chemoreception. Nearby prey are reached by rapidly crawling over&#13;
the sand surface, and prey at a distance are reached by using the foot to "sail"&#13;
to their location. In either case, contact with the prey is first made by the&#13;
propodium of the foot, rapidly followed by proboscis eversion. After contact&#13;
is made, the prey is stabbed by a radular tooth held by the buccal tube, poison&#13;
is injected into the wound, and engulfing of the worm begins. This entire&#13;
sequence occurs between the passage of waves, and the snail usually reburrows&#13;
to continue feeding before the next wave arrives.&#13;
The sexes in Hastula inconstans are separate. Mating takes place above the&#13;
sand while the animals are coupled and rolling freely in the surf, and&#13;
approximately 40 spherical eggs are later deposited in a capsule covering a&#13;
small piece of basalt. Larvae metamorphose when they are less than 1 mm in&#13;
length and reach 3-5 mm in length by late spring. Individuals grow between&#13;
0.5 and 0.8 mm per month, reaching a maximum size of 34 mm, which&#13;
suggests an average life-span of 3-4 years. Other hastulas with a proboscis&#13;
nearly identical in structure to that of H. inconstans exhibit similar life history&#13;
aspects, including habitat choice and prey specificity. It is suggested that&#13;
feeding types may not only be useful as a diagnostic characteristic, but also in&#13;
predicting basic life history aspects throughout the family.
</description>
<pubDate>Sun, 01 Jul 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1479</guid>
<dc:date>1979-07-01T00:00:00Z</dc:date>
<dc:creator>Miller, Bruce A</dc:creator>
</item>
<item>
<title>A Comparison of Aspects of the Biology of Paranemertes peregrina (Nemertea) from Bodega Harbor, California, and Washington State</title>
<link>http://hdl.handle.net/10125/1478</link>
<description>In Bodega Harbor, California, the nemertean Paranemertes&#13;
peregrina spawns in June or July. Adults in the study area were small in&#13;
comparison to worms found on two Washington mud flats. Population density&#13;
of active worms averaged 7.38 worms/m2, with much variation due to time of&#13;
day of low tides. Approximately 28 percent of the active population ate during&#13;
the low tide periods that were sampled. Prey included spionids, nephtyids,&#13;
polychaetes with capillary setae, and syllids (in decreasing importance). The&#13;
number of prey families in the diet of California nemerteans was higher&#13;
than in the two Washington mud flat populations and preferred nereid&#13;
prey was less abundant in California and comprised less of the total diet of&#13;
nemerteans there. Spionids were the major prey of California nemerteans in&#13;
spring and summer; nereids were the major prey in fall and winter. In food&#13;
preference tests, nemerteans showed negative responses to phoronids and&#13;
lumbrinerids and positive responses to Nephtys caecoides. In comparison to&#13;
three Washington populations, the population in Bodega Harbor was most&#13;
similar to a rocky intertidal population and much different from two mud flat&#13;
populations.
</description>
<pubDate>Sun, 01 Jul 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1478</guid>
<dc:date>1979-07-01T00:00:00Z</dc:date>
<dc:creator>Roe, Pamela</dc:creator>
</item>
<item>
<title>Studies of Leptospirosis in Natural Host Populations I. Small Mammals of Waipio Valley, Island of Hawaii</title>
<link>http://hdl.handle.net/10125/1477</link>
<description>The small Indian mongoose, Herpestes auropunctalus&#13;
(Carnivora: Viverridae), and the roof rat, Rattus rattus, and the Polynesian&#13;
rat, Rattus exulans (both Rodentia: Muridae), are abundant in Waipio Valley,&#13;
island of Hawaii. Two other murid rodents, the house· mouse, Mus musculus,&#13;
and the Norway rat, Rattus norvegicus, are sporadic or rare in occurrence. As&#13;
carriers of serotypes of the bacterium Leptospira interrogans (Spirochaetales:&#13;
Treponemataceae), which is transmissible to humans, this assemblage of&#13;
introduced mammals is of public health significance, for numerous cases of&#13;
leptospirosis, or Weil's disease, have been traced to the valley. Population&#13;
density of the mongoose was estimated at 2.3 per acre; for rats, it fluctuated&#13;
seasonally from I to 11 per acre. The serotypes icterohemorrhagiae and sejroe&#13;
were found in the mongoose in a 40:60 ratio by the kidney culture method.&#13;
Combined kidney culture and serological tests on 180 mongooses showed a&#13;
high of 34 percent overall infection in winter and a summer low of 9.4 percent.&#13;
Of 33 house mice tested by culture only, ballum was isolated from 21 and&#13;
icterohemorrhagiae from two. One isolation of icterohemorrhagiae was made&#13;
from four Norway rats examined. For 126 roof rats tested by serology and&#13;
kidney culture, 68 percent of adults and 26 percent of young were infected; and&#13;
for 175 Polynesian rats, 34 percent of adults and 26 percent of young were&#13;
infected. The Polynesian rat demonstrated a lesser persistence of the serum&#13;
titer phase of the disease than did the roof rat. Icterohemorrhagiae made up 95&#13;
percent and ballum the remaining 5 percent of infections in the roof rat. For&#13;
the Polynesian rat the ratio was 75: 25. Free-ranging rats under observation&#13;
for as long as 8 months acquired or lost infections, as determined by repeated&#13;
serological tests. The wet subtropical climate of Waipio Valley supports&#13;
conditions for transmission of leptospirosis among small mammals, and&#13;
possibly to humans, even in times of drought. No prominent differences were&#13;
observed in the infection rates in the lower valley at 30 ft above sea level and&#13;
1.7 miles inland at 120 ft. In the forested watershed of the valley rim at 3000 ft,&#13;
conditions of infection by species of host and by serotype of L. interrogans&#13;
matched elosely those found on the valley floor. Tests of 152 water samples&#13;
from streams, ponds, and taro patches resulted in isolations only of saprophytic&#13;
leptospires, although temperatures, salinities, and pH concentrations&#13;
appeared to be favorable for the support of pathogenic forms.
</description>
<pubDate>Sun, 01 Jul 1979 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/1477</guid>
<dc:date>1979-07-01T00:00:00Z</dc:date>
<dc:creator>Tomich, P Quentin</dc:creator>
</item>
</channel>
</rss>
