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  <title>Pacific Science Volume 58, Number 4, 2004</title>
  <link rel="alternate" href="http://hdl.handle.net/10125/2397" />
  <subtitle />
  <id>http://hdl.handle.net/10125/2397</id>
  <updated>2017-07-02T19:04:06Z</updated>
  <dc:date>2017-07-02T19:04:06Z</dc:date>
  <entry>
    <title>Distribution of the Chuuk Islands Giant Millipede, Acladocricus setigerus (Spirobolida: Rhinocricidae), and Identification of Its Defensive Compounds</title>
    <link rel="alternate" href="http://hdl.handle.net/10125/2747" />
    <author>
      <name>Buden, Donald W.</name>
    </author>
    <author>
      <name>Attygalle, Athula</name>
    </author>
    <author>
      <name>Wu, Xiaogang</name>
    </author>
    <id>http://hdl.handle.net/10125/2747</id>
    <updated>2015-06-08T22:49:54Z</updated>
    <published>2004-10-01T00:00:00Z</published>
    <summary type="text">Abstract: The spirobolidan millipede Acladocrieus setigerus (Silvestri, 1897)&#xD;
grows to at least 155 mm long and is so far known only from Chuuk Islands,&#xD;
Micronesia. It occurs mainly in well-shaded habitats, usually on the forest floor&#xD;
and on tree trunks. It sprays defensive secretions from paired, lateral ozopores&#xD;
on trunk segments; the major compounds, identified here for the first time, are&#xD;
benzoquinones. The secretion stains human skin a reddish brown and causes a&#xD;
slight burning sensation, occasionally followed by slight blistering and exfoliation.</summary>
    <dc:date>2004-10-01T00:00:00Z</dc:date>
    <dc:creator>Buden, Donald W.; Attygalle, Athula; Wu, Xiaogang</dc:creator>
  </entry>
  <entry>
    <title>A Prehistoric, Noncultural Vertebrate Assemblage from Tutuila, American Samoa</title>
    <link rel="alternate" href="http://hdl.handle.net/10125/2746" />
    <author>
      <name>Steadman, David W.</name>
    </author>
    <author>
      <name>Pregill, Gregory K.</name>
    </author>
    <id>http://hdl.handle.net/10125/2746</id>
    <updated>2015-06-08T22:49:54Z</updated>
    <published>2004-10-01T00:00:00Z</published>
    <summary type="text">Abstract: Ana Pe'ape'a is a small cave on the southern shore of Tutuila, American&#xD;
Samoa. Excavations at Ana Pe'ape'a yielded 13,600+ bones of small vertebrates,&#xD;
dominated (&gt;95%) by the nonnative Pacific Rat, Rattus exulans.&#xD;
Represented in the owl-derived bone deposit are two species that no longer occur&#xD;
on Tutuila, the Pacific Boa (Candoia bibroni) and the Sooty Crake (Porzana&#xD;
tabuensis). Based on bone counts, C. bibroni was the second most common species&#xD;
at the site. The third most common, the Sheath-tailed Bat (Emballonura semicaudata),&#xD;
is extremely rare on Tutuila today. Compared with bone records in&#xD;
nearby Tonga, we believe that the deposit at Ana Pe'ape'a, with a radiocarbon&#xD;
date of A.D. 445 to 640, is at least 1,000 yr too young to be dominated by extinct&#xD;
species.</summary>
    <dc:date>2004-10-01T00:00:00Z</dc:date>
    <dc:creator>Steadman, David W.; Pregill, Gregory K.</dc:creator>
  </entry>
  <entry>
    <title>New Hyocrinid Crinoids (Echinodermata) from Submersible Investigations in the Pacific Ocean</title>
    <link rel="alternate" href="http://hdl.handle.net/10125/2745" />
    <author>
      <name>Roux, Michel</name>
    </author>
    <id>http://hdl.handle.net/10125/2745</id>
    <updated>2012-08-14T21:07:22Z</updated>
    <published>2004-10-01T00:00:00Z</published>
    <summary type="text">Abstract: A few specimens belonging to the deep-sea family Hyocrinidae&#xD;
(stalked Crinoidea, Echinodermata) collected by submersible in the eastern and&#xD;
western Pacific Ocean are described. Laubierierinus pentagonalis, n. genus, n. sp.,&#xD;
from the North Fiji Rise is the first discovery of a hyocrinid crinoid with a&#xD;
pentaradially symmetrical stalk. Hyocrinus biscoitoi, n. sp., from the East Pacific&#xD;
Rise attains large size and has close affinities with H. giganteus from Horizon&#xD;
Seamount. Additional information is given concerning H. foelli found near cold&#xD;
seeps on the Mexican continental margin; H. cyanae, previously collected on&#xD;
New Caledonian slopes; and Calamoerinus diomedae from the Cocos Ridge and&#xD;
Galapagos slopes. For the latter, the first young specimens known document&#xD;
ontogenetic trends in this famous species.</summary>
    <dc:date>2004-10-01T00:00:00Z</dc:date>
    <dc:creator>Roux, Michel</dc:creator>
  </entry>
  <entry>
    <title>Population Size and Natural History of Mariana Fruit Bats (Chiroptera: Pteropodidae) on Sarigan, Mariana Islands</title>
    <link rel="alternate" href="http://hdl.handle.net/10125/2744" />
    <author>
      <name>Wiles, Gary J.</name>
    </author>
    <author>
      <name>Johnson, Nathan C.</name>
    </author>
    <id>http://hdl.handle.net/10125/2744</id>
    <updated>2015-06-08T22:49:54Z</updated>
    <published>2004-10-01T00:00:00Z</published>
    <summary type="text">Abstract: Based on count results, we estimated the population of Mariana fruit&#xD;
bats (Pteropus mariannus Desmarest) on Sarigan, Mariana Islands, to number&#xD;
150-200 bats in 1999, 185-235 bats in 2000, and about 300-400 bats in 2001.&#xD;
Our results, plus those of two previous surveys, indicate that bat abundance on&#xD;
the island probably remained relatively stable at about 125-235 animals during&#xD;
much of the period from 1983 to 2000, then increased suddenly in 2001, most&#xD;
likely due to immigration from a neighboring island. Sarigan's population differs&#xD;
from those of larger islands in the archipelago by usually having smaller roost&#xD;
sizes, typically 3-75 bats, and large numbers of solitary bats that at times comprise&#xD;
up to half of the population. Colonies and smaller aggregations were&#xD;
composed primarily of harems with multiple females, whereas a nearly equal sex&#xD;
ratio occurred among solitary animals. Colonies roosted in isolated coconut&#xD;
trees in open grasslands and in native forest stands of various sizes, but avoided&#xD;
dense coconut forest. An estimated 30-50% of harem and solitary females possessed&#xD;
young in July 1999. Bats were recorded feeding on just six species of&#xD;
plants, which partly reflects the island's impoverished flora. We speculate that&#xD;
fruit bat abundance on Sarigan is limited primarily by food availability rather&#xD;
than hunting losses, in contrast to some other islands in the Marianas. Our study&#xD;
supports the contention that populations of P. mariannus in the northern Marianas&#xD;
are usually sedentary, but that interisland movements of larger numbers&#xD;
of bats may occur rarely.</summary>
    <dc:date>2004-10-01T00:00:00Z</dc:date>
    <dc:creator>Wiles, Gary J.; Johnson, Nathan C.</dc:creator>
  </entry>
  <entry>
    <title>A Pygmy Blue Whale (Cetacea: Balaenopteridae) in the Inshore Waters of New Caledonia</title>
    <link rel="alternate" href="http://hdl.handle.net/10125/2743" />
    <author>
      <name>Borsa, Philippe</name>
    </author>
    <author>
      <name>Hoarau, Galice</name>
    </author>
    <id>http://hdl.handle.net/10125/2743</id>
    <updated>2012-08-14T21:07:22Z</updated>
    <published>2004-10-01T00:00:00Z</published>
    <summary type="text">Abstract: The occurrence of a blue whale is reported for the first time for the&#xD;
New Caledonian archipelago. The whale, a juvenile male in poor condition,&#xD;
entered the shallow inshore waters of the coral reef lagoon (220 19-24' S, 1660&#xD;
46-52' E) where it spent at least 1 month until it was killed by whaler sharks on&#xD;
27 January 2002. Live observations, examination of photographic documents,&#xD;
and skull osteology indicated that this was a pygmy blue whale, Balaenoptera&#xD;
musculus brevicauda. Nucleotide sequences of PCR-amplified fragments of its&#xD;
mitochondrial DNA were determined and compared with the few published&#xD;
homologous sequences of North Atlantic blue whales, B. m. musculus, but no&#xD;
obvious differences were apparent.</summary>
    <dc:date>2004-10-01T00:00:00Z</dc:date>
    <dc:creator>Borsa, Philippe; Hoarau, Galice</dc:creator>
  </entry>
  <entry>
    <title>Spatial Distribution of Fish Larvae in a Bay of the Gulf of California (June and November 1997)</title>
    <link rel="alternate" href="http://hdl.handle.net/10125/2742" />
    <author>
      <name>Peguero-Icaza, Martha</name>
    </author>
    <author>
      <name>Sanchez-Velasco, Laura</name>
    </author>
    <id>http://hdl.handle.net/10125/2742</id>
    <updated>2012-08-14T21:07:22Z</updated>
    <published>2004-10-01T00:00:00Z</published>
    <summary type="text">Abstract: Bahia Concepcion is one of the largest coastal bodies of water on the&#xD;
peninsular side of the Gulf of California, which is characterized by great fish&#xD;
species diversity. Spatial distributions of fish larvae in Bahia Concepcion during&#xD;
June and November 1997 were analyzed; these months were representative&#xD;
of the extreme hydrographic conditions during an annual cycle in the Gulf.&#xD;
Zooplankton samples (333-(mu)m conical net) and conductivity, temperature, and&#xD;
depth data were obtained at each sampling station. The Bray-Curtis dissimilarity&#xD;
index defined three groups of stations in June (mouth, central, and interior) and&#xD;
two in November (mouth and central-interior), which vary in species composition&#xD;
and dominance. In June, Gerreidae (Eucinostomus gracilis) and Clupeidae&#xD;
(Opisthonema sp.) larvae were the dominant species in the bay mouth; Sciaenidae&#xD;
type 1, Clupeidae (Harengula thrissina), and Pomacentridae (Stegastes rectifraenum)&#xD;
larvae were the dominant species in the central bay; and Gerreidae (E.&#xD;
dowii) larvae in the bay interior. The differentiation of three groups is associated&#xD;
with variations in hydrographic conditions recorded from the mouth to the bay&#xD;
interior, coinciding with a well-defined thermocline throughout the bay as a&#xD;
result of weak winds prevailing in the central Gulf region. In November, Mullidae&#xD;
and Clupeidae (Etrumeus teres) larvae were the dominant taxa in the bay&#xD;
mouth, and Gobiidae (Ilypnus gilberti) and Blenniidae (Hypsoblennius gentilis)&#xD;
larvae dominated in the central and interior bay. The similarity of the larval&#xD;
composition of the central and interior bay is associated with a straight spatial&#xD;
gradient of temperature and salinity and homogeneity in the water column; this&#xD;
condition was caused by strong winds and tides that affect the region in late fall.&#xD;
In addition, the presence of mesopelagic species (e.g., Vinciguerria lucetia) in the&#xD;
bay interior during November indicates a clear influence of the Gulf waters in&#xD;
the bay at that time, possibly as a result of intensive mixing.</summary>
    <dc:date>2004-10-01T00:00:00Z</dc:date>
    <dc:creator>Peguero-Icaza, Martha; Sanchez-Velasco, Laura</dc:creator>
  </entry>
  <entry>
    <title>Tropical Transpacific Shore Fishes</title>
    <link rel="alternate" href="http://hdl.handle.net/10125/2730" />
    <author>
      <name>Robertson, D Ross</name>
    </author>
    <author>
      <name>Grove, Jack S.</name>
    </author>
    <author>
      <name>McCosker, John E.</name>
    </author>
    <id>http://hdl.handle.net/10125/2730</id>
    <updated>2015-06-08T22:49:54Z</updated>
    <published>2004-10-01T00:00:00Z</published>
    <summary type="text">Abstract: Tropical transpacific fishes occur on both sides of the world's largest&#xD;
deep-water barrier to the migration of marine shore organisms, the 4,000- to&#xD;
7,000-km-wide Eastern Pacific Barrier (EPB). They include 64 epipelagic oceanic&#xD;
species and 126 species of shore fishes known from both the tropical eastern&#xD;
Pacific (TEP) and the central and West Pacific. The broad distributions of 19&#xD;
of 39 circumglobal transpacific species of shore fishes offer no clues to the origin&#xD;
of their TEP populations; TEP populations of another 19 with disjunct Pacific&#xD;
distributions may represent isthmian relicts that originated from New World&#xD;
populations separated by the closure of the Central American isthmus. Eighty&#xD;
species of transpacific shore fishes likely migrated eastward to the TEP, and 22&#xD;
species of shore fishes (12 of them isthmian relicts) and one oceanic species&#xD;
likely migrated westward from the TEP. Transpacific species constitute ~12%&#xD;
of the TEP's tropical shore fishes and 15-20% of shore fishes at islands on the&#xD;
western edge of the EPB. Eastward migrants constitute ~7% of the TEP's&#xD;
shore-fish fauna, and a similar proportion of TEP endemics may be derived&#xD;
from recent eastward immigration. Representation of transpacific species in&#xD;
different elements of the TEP fauna relates strongly to adult pelagic dispersal&#xD;
ability-they constitute almost all the epipelagic oceanic species, ~25% of&#xD;
the inshore pelagic species, but only 10% of the demersal shore fishes. Taxa&#xD;
that have multiple pelagic life-history stages are best represented among the&#xD;
transpacific species. Among demersal teleosts that have pelagic larvae, pelagic&#xD;
spawners are better represented than demersal spawners among transpacific&#xD;
species, perhaps because offshore larval development and longer pelagic larval&#xD;
durations provide the former with greater dispersal capabilities. There are&#xD;
strong phylogenetic effects on representation in the transpacific fauna: (1) elasmobranchs&#xD;
are proportionally better represented than teleosts, even teleosts&#xD;
with more pelagic life-history stages; (2) a pelagic juvenile stage with great dispersal&#xD;
potential allows tetraodontiforms that produce demersal or pelagic eggs&#xD;
to be well represented; and (3) various speciose central Pacific families with&#xD;
"adequate" larval dispersal characteristics lack transpacific species. El Niiios&#xD;
potentially enhance eastward migration by increasing eastward flow and halving&#xD;
transit times across the EPB. However, that effect may be offset by low productivity&#xD;
and high temperatures in those eastbound flows. There is little clear&#xD;
evidence of strongly increased migration across the EPB during El Niiios, including&#xD;
recent extreme events (1982-1983 and 1997-1998). During such events&#xD;
shore fishes in the TEP experience range expansions and become locally abundant at marginal areas such as the Galapagos, changes that can be confused with&#xD;
increased migration across the EPB. Although there is a strong bias toward&#xD;
eastward migration among the transpacific shore fishes, there likely is much&#xD;
more westward migration than previously realized: 20-25% of transpacific species&#xD;
may have migrated in that direction. Stronger eastbound than westbound&#xD;
currents can account for this bias. Westward migrants have better developed&#xD;
pelagic dispersal characteristics than many eastward migrants, suggesting that&#xD;
westward migration is more difficult. Many westward migrants associate with&#xD;
flotsam and flotsam-mediated migration is more likely to be westward. All&#xD;
westward migrants occur at Hawai'i, but only about one-fifth of them at the&#xD;
Marquesas. This bias may be due to: Hawai'i being a larger target and in the&#xD;
path of most of the flotsam dispersal from the TEP; an eastward current that&#xD;
impinges on the Marquesas, reducing westward arrivals; and most propagules&#xD;
dispersing toward the tropical Marquesas originating in the temperate eastern&#xD;
Pacific. However, the Hawaiian Islands also are much better sampled than the&#xD;
Marquesas. Although the TEP reef-fish fauna may be depauperate relative to&#xD;
that of the Indo-Malayan "center of diversity," it is as rich as the faunas of islands&#xD;
on the western side of the EPB. Hence a preponderance of eastward migration&#xD;
does not represent a response to a richness gradient across that barrier.&#xD;
There is little evidence that a paucity of ecological groups in the native TEP&#xD;
fauna is primarily responsible for the structure of the eastward-migrant fauna.&#xD;
Rather, eastward migrants may simply represent a cross section of those in the&#xD;
donor fauna, tempered by phylogenetic variation in dispersal ability. Because&#xD;
few central Pacific fishes can live only on live corals and coral reefs, the rarity of&#xD;
such reefs in the TEP is unlikely to strongly limit eastward migration. Differences&#xD;
between oceanic and adjacent continental reef-fish faunas in the West&#xD;
Pacific indicate that each is strongly tied to its respective habitat. Hence, the&#xD;
rarity in the TEP of the (overwhelmingly) most abundant habitat present in the&#xD;
central Pacific-tropical oceanic reefs-may strongly limit migration in both&#xD;
directions across the EPB: there is little suitable habitat for eastward migrants in&#xD;
the TEP and few suitable species and tiny source populations for westward migrants.&#xD;
The global effects that oceanic/continental habitat differences have on&#xD;
reef-fish biogeography need further assessment. Genetic data on ~18% of the&#xD;
transpacific species indicate: that conspecific populations of oceanic species&#xD;
(especially) and shore fishes are genetically well connected across the EPB; that&#xD;
circumtropical taxa in the TEP include isolated isthmian relicts and recent&#xD;
eastward migrants; that all five TEP species of one circumtropical genus (Thalassoma)&#xD;
were derived by several eastward invasions after the closure of the&#xD;
Isthmus of Panama; that some isolated Hawaiian central Pacific populations&#xD;
were established by postisthmian invasion from the TEP; and that Indo-central&#xD;
Pacific species unsuspectedly can co-occur with their endemic sibling sisters&#xD;
in the TEP. Genetic data support distributional data that indicate a strong&#xD;
preponderance of eastward migration across the EPB but also more westward&#xD;
migration than previously thought. Future genetic studies should resolve&#xD;
a question that distributional data cannot: how many widespread presumed&#xD;
eastward-migrant transpacific species actually originated by westward migration&#xD;
from the TEP?</summary>
    <dc:date>2004-10-01T00:00:00Z</dc:date>
    <dc:creator>Robertson, D Ross; Grove, Jack S.; McCosker, John E.</dc:creator>
  </entry>
  <entry>
    <title>58:4 Table of Contents - Pacific Science</title>
    <link rel="alternate" href="http://hdl.handle.net/10125/2729" />
    <author>
      <name />
    </author>
    <id>http://hdl.handle.net/10125/2729</id>
    <updated>2012-08-14T21:07:22Z</updated>
    <published>2004-10-01T00:00:00Z</published>
    <dc:date>2004-10-01T00:00:00Z</dc:date>
  </entry>
</feed>

