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<title>Pacific Science Volume 49, Number 1, 1995</title>
<link>http://hdl.handle.net/10125/1116</link>
<description/>
<pubDate>Fri, 24 May 2013 10:27:29 GMT</pubDate>
<dc:date>2013-05-24T10:27:29Z</dc:date>
<item>
<title>Toward Ethical Treatment of Animals in Hawai'i's Natural Areas</title>
<link>http://hdl.handle.net/10125/2277</link>
<description>Human alienation from nature is evidenced by minimal understanding&#13;
of interrelationships in the wild and an emphasis on individual wild&#13;
animals. Different viewpoints (utilitarian, biocentric, and theocentric) about the&#13;
natural world and the place of humans in it color ideas about management of&#13;
natural areas and the species therein. Decisions about nature should consider a&#13;
complex of human values including the economic, aesthetic, spiritual, ecological,&#13;
and humane, along with a preservation ethic for the future. Control of introduced,&#13;
or alien, animals in Hawai'i, where endangerment and extinction&#13;
rates of native species are among the highest in the world, and where alien&#13;
species cause severe degradation and disappearance of near-natural communities,&#13;
has recently become controversial as a result of confrontational activities&#13;
by animal rights activists. However, people who "speak for" animals in the&#13;
world involve a wide variety of groups, including natural resource managers,&#13;
hunters and fishers, scientists, agriculturists, conservationists, and humane and&#13;
animal rights groups. An ethical system for wild animals must make good-faith&#13;
efforts to protect all human values. A good-faith approach to conflict presumes&#13;
that most groups have codes of right and wrong (ethics), even though some may&#13;
not be as completely developed as others. We need to "outgrow" narrow views&#13;
of nature by better understanding human relationships to it through meaningful&#13;
participation (hunting, management, scientific study, observation, etc.). Actions&#13;
and nonactions must be governed by a holistic and flexible ethic practically&#13;
applied to different conflict situations.
</description>
<pubDate>Sun, 01 Jan 1995 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/2277</guid>
<dc:date>1995-01-01T00:00:00Z</dc:date>
<dc:creator>Stone, Charles P</dc:creator>
</item>
<item>
<title>Why Do Introduced Species Appear to Devastate Islands More Than Mainland Areas?</title>
<link>http://hdl.handle.net/10125/2276</link>
<description>Island biotas are viewed popularly as much more fragile than&#13;
those of mainland areas and much more prone to damage from invaders. There&#13;
are far too few data to assess this view thoroughly; for example, failed invasions&#13;
are often unrecorded, and claims that an introduced species has displaced a native&#13;
one are often based on correlated population changes rather than experiment&#13;
and/or detailed field observations. If there is a tendency for invasions to affect&#13;
island communities more than mainland ones, it is far from universal; virtually&#13;
every kind of damage wrought by invaders on islands has also been wrought in&#13;
mainland areas. It is unlikely that, by virtue of their reduced species richness&#13;
alone, island communities pose less "biotic resistance" to invaders than mainland&#13;
communities do. Rather, certain entire groups of species, like terrestrial&#13;
mammals, are often missing from islands, and these absences can predispose&#13;
certain invaders to be especially likely to survive and to produce particular impacts.
</description>
<pubDate>Sun, 01 Jan 1995 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/2276</guid>
<dc:date>1995-01-01T00:00:00Z</dc:date>
<dc:creator>Simberloff, Daniel</dc:creator>
</item>
<item>
<title>Distribution and Ecology of Birds of Japan</title>
<link>http://hdl.handle.net/10125/2275</link>
<description>The effects of island biogeography are clearly seen in the avifauna&#13;
of Japan. Species composition and distribution reflect Japan's geographic,&#13;
climatic, vegetational, topographical, and geological characteristics. It is a&#13;
country composed primarily of mountainous, forested islands that lies off the&#13;
coast of a continent rich in bird life. Though Japan has a wide range of climates&#13;
and diverse forest habitats, the terrestrial and freshwater avifauna is depauperate&#13;
when compared with species, family, and order diversity on the&#13;
nearby continent, which is both larger in total area and more diverse in habitats.&#13;
However, the bird groups that do have higher species diversity in Japan&#13;
than in the Asian mainland are seabirds. The large, productive ocean area and&#13;
small, isolated islands provide them with foraging and nesting sites, and the&#13;
long geographic range of Japan allows seabirds from both northern and&#13;
southern regions to nest in the Islands. Island biogeography also affects the&#13;
ecology of many terrestrial species. Niche shift and expansion of foraging and&#13;
parasitic behaviors are seen in populations established on islands where the&#13;
species composition does not include certain competitors. The terrestrial species&#13;
resident on small islands have developed unique breeding behavior, in comparison&#13;
with their conspecifics on larger islands, such as smaller clutch size,&#13;
exaggerated begging behavior, and longer parental care in small-island populations&#13;
of Varied Tits, Parus varius Temminck &amp; Schlegel.
</description>
<pubDate>Sun, 01 Jan 1995 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/2275</guid>
<dc:date>1995-01-01T00:00:00Z</dc:date>
<dc:creator>Higuchi, Hiroyoshi; Minton, Jason; Katsura, Chieko</dc:creator>
</item>
<item>
<title>Social Structure and Reproductive Systems of Tramp Versus Endemic Ants (Hymenoptera: Formicidae) of the Ryukyu Islands</title>
<link>http://hdl.handle.net/10125/2274</link>
<description>Currently, 126 ant species have been recorded from the Ryukyu&#13;
Islands, Japan. Of these, 54 species, many of which are probably new to science,&#13;
have not yet been identified. A survey on species-habitat relationships&#13;
made on the island of Okinawa indicated that open lands were occupied predominantly&#13;
by tramp species, but primary forests contained many endemic&#13;
species. Colony structure and the reproductive system of the eurychoric species&#13;
are briefly reviewed and discussed. A secondary polygynous and polydomous&#13;
system is predominant in these species. This system is characterized by intranidal&#13;
mating, which may reduce the risk in nuptial flights and ensure the&#13;
adoption of new queens. A diversity in morphology and behavior, especially in&#13;
males, seems to develop, provided the workers care for them. Stenochoric forest&#13;
species are mostly monogynous.
</description>
<pubDate>Sun, 01 Jan 1995 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/2274</guid>
<dc:date>1995-01-01T00:00:00Z</dc:date>
<dc:creator>Yamauchi, Katsusuke; Ogata, Kazuo</dc:creator>
</item>
<item>
<title>Variation in Reproductive Strategy of the Tropical Paper Wasp, Ropalidia fasciata (Hymenoptera: Vespidae), in Okinawa in Relation to Island Environmental Conditions</title>
<link>http://hdl.handle.net/10125/2273</link>
<description>The tropical paper wasp, Ropalidia (Icariola) fasciata (F.), nests&#13;
on leaves of gramineous plants (Miscanthus sinensis Andus. and sugarcane) in&#13;
Okinawa, where there are frequent, strong typhoons. In Taiwan and Java,&#13;
where the effects of typhoons are less severe, most nests are on tree twigs. A&#13;
similar difference is seen in nests of Ropalidia (I.) marginata (Lepeletier) in the&#13;
Northern Mariana Islands and in India. Okinawan R. fasciata also exhibits&#13;
quite flexible social behavior, low frequency of intranidal dominance behavior,&#13;
construction of satellite and multiple-comb nests, absconding swarming, and&#13;
initiation and development of nests in late autumn. Study of the divergence of&#13;
social habits in eusocial wasps on Pacific Islands will enhance our understanding&#13;
of social evolution in insects.
</description>
<pubDate>Sun, 01 Jan 1995 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/2273</guid>
<dc:date>1995-01-01T00:00:00Z</dc:date>
<dc:creator>Ito, Yosiaki</dc:creator>
</item>
<item>
<title>Evolution of Hawaiian Ferns and Fern Allies in Relation to Their Conservation Status</title>
<link>http://hdl.handle.net/10125/2272</link>
<description>Evolutionary and conservational differences between Hawaiian&#13;
pteridophytes and angiosperms involve differences in life histories (free-living&#13;
generations, fertilization, and spore dispersal). Very high base chromosome&#13;
numbers characterize the homosporous pteridophytes. Long-distance spore&#13;
dispersal took place mainly from Old World and pantropical ancestors, accounting&#13;
for some 80% of the taxa. The ratio of native pteridophyte to angiosperm&#13;
taxa in Hawai'i averages roughly 1: 6, much higher than in continental&#13;
floras with 1: 14. Two hundred twenty-four pteridophyte taxa, including hybrids&#13;
and naturalizations, are known in Hawai'i. The 170 native orthospecies&#13;
include endemics (highly variable taxa with polymorphies involving one or&#13;
more characters, monophyletic species swarms, and solitary endemics) as well&#13;
as nonendemics. Hybrid nothospecies compose an important additional component,&#13;
as do naturalized orthospecies. Most of the hybrids are sterile intermediates&#13;
that propagate by vegetative means; sexual hybrids are rare. The percentage&#13;
of naturalized species is only one-fourth that of angiosperms. Hawaiian&#13;
pteridophytes have evolved much more slowly than the angiosperms, as shown&#13;
by lower endemism (75% versus 91% overall and relatively fewer one- or two-island&#13;
endemics) and much smaller species swarms (average 1.5 versus 16.0 descendants&#13;
from each introduction in the 20 most species-rich genera, respectively). Anticipated listing of Hawaiian rare and endangered fern species&#13;
will probably comprise ca. 17% of the natives, including four believed to be&#13;
extinct. Naturalized species compose only one-fourth of the percentage in angiosperms,&#13;
and very few are pests. Habitat destruction by humans and feral&#13;
mammals is the major conservation problem. Although artificial spore banks&#13;
and whole-plant culture may help save some rare pteridophytes, the most&#13;
promising procedure is establishment of natural preserves.
</description>
<pubDate>Sun, 01 Jan 1995 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/2272</guid>
<dc:date>1995-01-01T00:00:00Z</dc:date>
<dc:creator>Wagner, Warren Herb Jr</dc:creator>
</item>
<item>
<title>Phytogeography and Ecology of Scalesia (Compositae) Endemic to the Galapagos Islands</title>
<link>http://hdl.handle.net/10125/2271</link>
<description>Scalesia (Compositae), a genus endemic to the Galapagos Islands,&#13;
consists of 12 shrubby species distributed in the lowland dry zone and&#13;
three tree species found in the mid-elevation moist zone. They are completely&#13;
allopatric in distribution. All the species have herbaceous traits: fast growth,&#13;
soft wood, large pith at the center of trunk, and flowering within 1 yr after&#13;
germination (in greenhouse). The tree species Scalesia pedunculata Hook. f. is&#13;
shade-intolerant and heliophilous, and predominates as a monoculture in the&#13;
moist zone of the four larger high-elevation islands. In ecological succession, it&#13;
functions as pioneer, successor, and climax canopy plant. Even at climax or&#13;
maturity of this monodominant forest, the canopy is not accompanied by&#13;
young generations beneath owing to its shade-intolerance. The canopy population&#13;
of postmature forest dies back nearly synchronously. A new generation&#13;
then develops to build new forest. The progression from germination to maturity,&#13;
and further to senescence and die back, is a self-cyclic succession, without&#13;
change of dominant species. Over much of its range, S. pedunculata is endangered&#13;
by the effects of past agricultural exploitation or heavy browsing by&#13;
free-ranging goats, pigs, and donkeys; however, the population on the north&#13;
side of Isla Santa Cruz has been preserved in good condition in the Galapagos&#13;
National Park.
</description>
<pubDate>Sun, 01 Jan 1995 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/2271</guid>
<dc:date>1995-01-01T00:00:00Z</dc:date>
<dc:creator>Itow, Syuzo</dc:creator>
</item>
<item>
<title>The Hawaiian Islands as a Model System for Ecosystem Studies</title>
<link>http://hdl.handle.net/10125/2270</link>
<description>The Hawaiian Islands encompass an extraordinary range of&#13;
variation in climate and soil age in a small area; the younger volcanoes are also&#13;
extraordinary for their lack of variation in relief or topography, parent material,&#13;
and biota (before widespread invasions by alien species). Consequently,&#13;
in Hawai'i the independent and interactive effects of temperature, precipitation,&#13;
and soil age on ecosystem structure and function can be evaluated with a power&#13;
that is beyond the reach of studies elsewhere. Not only are extreme conditions&#13;
well represented in Hawai'i, but there are also complete gradients between the&#13;
extremes, allowing the determination of the relationships as well as the differences&#13;
among sites. My colleagues and I have established two sets of sites that&#13;
make use of these gradients: the Mauna Loa Environmental Matrix, a set of&#13;
lava flows ('a'a versus pahoehoe, old versus young) that cover a broad elevational&#13;
range on the wet east versus dry northwest flank of Mauna Loa; and a&#13;
chronosequence of sites that reaches from Kilauea (~300 yr old) to Kaua'i&#13;
(~4,100,000yr old) at 1200 m elevation, 2500 mm annual precipitation. These&#13;
sites are being used to determine climatic and developmental controls of ecosystem&#13;
function. I report some of the early results here.
</description>
<pubDate>Sun, 01 Jan 1995 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/2270</guid>
<dc:date>1995-01-01T00:00:00Z</dc:date>
<dc:creator>Vitousek, Peter M</dc:creator>
</item>
<item>
<title>Preface</title>
<link>http://hdl.handle.net/10125/2269</link>
<pubDate>Sun, 01 Jan 1995 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/2269</guid>
<dc:date>1995-01-01T00:00:00Z</dc:date>
</item>
<item>
<title>49:1 Table of Contents - Pacific Science</title>
<link>http://hdl.handle.net/10125/2268</link>
<pubDate>Sun, 01 Jan 1995 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/2268</guid>
<dc:date>1995-01-01T00:00:00Z</dc:date>
</item>
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