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<title>Ph.D. - Zoology</title>
<link>http://hdl.handle.net/10125/2173</link>
<description/>
<pubDate>Tue, 18 Jun 2013 21:05:11 GMT</pubDate>
<dc:date>2013-06-18T21:05:11Z</dc:date>
<item>
<title>Isolation, characterization and expression of limb patterning genes in Euprymna scolopes (Mollusca : Cephalopoda)</title>
<link>http://hdl.handle.net/10125/20929</link>
<description>Thesis (Ph.D.)--University of Hawaii at Manoa, 2008.; Cephalopod arms and tentacles have a considerable degree of patterning along their orthogonal axes. These appendages are non-homologous to other structures outside the Mollusca and are a structural novelty within the taxon. This work reports the isolation of cDNA transcripts from the aforementioned genes from the sepiolid Euprymna scolopes, their molecular characterization and corresponding developmental expression patterns. Also included is a general description of the organogenesis of E. scolopes  illustrated with photomicrographs of histological serial sections, a report on artificial fertilization trails, embryonic growth rates under different temperature regimes, and the recovery of 17 additional cDNA transcripts, 10 of which are full-length cds from developmentally important genes. This later body of information represents a valuable tool for the future use of this squid as a cephalopod model system for developmental studies.; Esc-BMP2/4 was expressed on the aboral side of the arm buds and later as a wide band over the entire length of each arm and tentacle, suggesting a role in growth and/or dorso-ventral patterning. In general,  Esc-BMP2/4 expression was highly dynamic and pleiotropic; gene transcripts were also detected in the developing brain, eyes, buccal mass, gut, gills, branchial hearts, funnel, mantle, fins, and all hard or cartilaginous structures.; Esc-Dll expression was assessed by immunolocalization of the anti-Dll most commonly used in comparative studies across taxa. Arm primordia, budding arms and later the tip of the developing arms and tentacles were strongly immunoreactive, in agreement with a possible gene function in outgrowth and proximo-distal patterning of these appendages. The overall results obtained support the proposed Dll roles in the development of body wall outgrowths, appendages, nervous system, and sensory structures.; Esc-Wnt1 transcripts were detected in arms and tentacles as a mesodermal, hairpin-like expression in mid and late embryonic stages (23-27), suggesting a role in the elongation of the appendages, but might also be related to the organization of their muscular mass. Esc-Wnt4  and Esc-Wnt5 expression was also analyzed in embryos stages 23 to 27; the hybridization signal in their appendages was mesodermal,  Esc-Wnt4 at the base and both edges of each limb and always stronger at the posterior side, and Esc-Wnt5 first in the dorsal distal mesenchyme of the limbs and later throughout the appendages.; Esc-ap and Esc-hh were not expressed in the arm crown in patterns consistent with roles in growth or axial organization of arms and tentacles, but with patterning of the brachial nervous system. Other conspicuous expression patterns suggest an Esc-ap role in eye and neural development, particularly for olfaction and vision, and  Esc-hh in gut and neural development. Esc-fng was transiently expressed at the tip of the differentiating arms and later in the distal ring of the suckers. Both expression patterns could be associated with the formation of borders; a possible link of the early expression to dorso-ventral patterning is also discussed. Other conspicuous Esc-fng  expression patterns could be linked to vasculogenesis.; Gene expression in the developing arms and tentacles of E. scolopes  did not conform fully to the UGPLD. The expression patterns of the putative Esc-Dll, Esc-BMP2-4, and the Esc-Wnts suggest that they could play important roles in the growth and patterning of these appendages; this needs to be confirmed by functional analysis.; Results from genetic, molecular, and developmental studies have shown that the limbs of Drosophila and vertebrates have remarkable similarities in the molecular instructions that convey the positional information that is required for the patterning of their orthogonal axes. The parsimonious explanations for parallels in the genetic programs of two animal lineages that diverged over 500 mya are independent co-option of homologous genes for similar functions or the conservation of an ancestral genetic program. One version of a 'Universal Genetic Program for Limb Development' (UGPLD) contains the following genes: apterous/Lhx2-9, decapentaplegic/Bone Morphogenic Protein, Distal-less/Dllx, fringe/Radical fringe, hedgehog/Sonic hedgehog, and wingless/Wnt1. These genes have never been analyzed as a group in an invertebrate taxon other than Arthropoda.; Includes bibliographical references (leaves 272-329).; Also available by subscription via World Wide Web; 348 leaves, bound 29 cm
</description>
<pubDate>Tue, 01 Jan 2008 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/20929</guid>
<dc:date>2008-01-01T00:00:00Z</dc:date>
<dc:creator>Farfan, Blanca Claudia</dc:creator>
</item>
<item>
<title>Bioenergetics and swimming efficiency of juvenile scalloped hammerhead sharks, Sphyrna lewini, in Kaneohe Bay, Oahu, Hawaii</title>
<link>http://hdl.handle.net/10125/18160</link>
<description>The goal of this study was to determine the energetic
requirements of juvenile scalloped hammerhead sharks (Sphyrna
lewini) in Kaneohe Bay, Oahu, Hawaii using a multidisciplinary
approach. A large flume/respirometer (635 1)
was constructed to determine the critical swimming speeds
(Ucrit )' swimming kinematics (tailbeat frequency, tailbeat
amplitude, and stride length), and oxygen consumption rates
(V02 ) of juvenile sharks over a range of swimming speeds (U).
Swimming kinematics were also compared with unconstrained
sharks in a seawater pond. These experiments indicated that
tailbeat frequency (TBF) and water temperature could be used
as a predictor of U and V02 for free-swimming sharks in the
field; however, the flume affected the sharks' swimming
kinematics at slow speeds. The flume and pond kinematic
comparisons were used to correct for flume effects on sharks'
V02.
An acoustic tailbeat-sensing transmitter was designed
and constructed to quantify activity and energy consumption
of free-swimming hammerhead shark pups in Kaneohe Bay.
Sharks with transmitters behaved similarly to uninstrumented
sharks, but incurred a 28% increase in cost of transport due
to increased drag from the transmitters. These data were
used to correct for the effects of the transmitter on freeswimming
sharks in the field. Sharks tracked in Kaneohe Bay with tailbeat transmitters
exhibited increased U during dawn and dusk, while sharks
tracked in the warmer summer months had higher activity rates
and metabolic rates (MR) than a shark tracked during the
winter. Sharks tracked in this study had higher MR than
those measured for other species of tropical sharks and, as a
result, require higher daily rations. Low and negative
growth rates determined from sharks in the Bay and declining
catch rates over the season suggest that a large percentage
of the pups in Kaneohe Bay may starve as the result of their
high metabolic requirements. Although prey do not appear to
be li~itingi lack of foraging experience compounded by a high
daily metabolic demand may explain why sharks lose weight
during summer months. Those pups that survive the winter
experience lower MR due to seasonal temperature decline and
less competition as the result of high neonatal mortality.
x, 130 leaves, bound : ill. (some col.) ; 29 cm.; Missing page 74.
</description>
<pubDate>Sat, 01 Aug 1998 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/18160</guid>
<dc:date>1998-08-01T00:00:00Z</dc:date>
<dc:creator>Lowe, Christopher G</dc:creator>
</item>
<item>
<title>The advantage of juvenile coloration in reef fishes</title>
<link>http://hdl.handle.net/10125/18159</link>
<description>Juvenile reef fishes often have a color pattern different from that of adults. It
has been theorized that this reduces the aggression received by juveniles from adult
conspecifics. This was tested using two species of Labroides cleaning wrasses in which
certain-sized individuals can quickly shift back and forth between the adult and juvenile
color patterns. Adult Labroides phthirophagus has the same single-male grouping
social structure as previously described for L. dimidiatus. Small L. phthirophagus and
L. dimidiatus in juvenile coloration shifted to adult coloration when isolated and then
quickly shifted back to juvenile coloration when chased by an adult conspecific female.
In L. phthirophagus the adult females attacked small cleaners more frequently when
they displayed the adult color pattern, indicating that juvenile coloration gives some
protection from conspecific aggression. Two other species oflabrids, Thalassoma
duperrey and Coris gaimard, showed the ability to shift back to juvenile coloration
when aggression was received from con specific adults, although the shift was not nearly
as rapid as seen in Labroides species.
Dascyllus albisella and Zebrasomajlavescens, common reef fishes, preferred to
solicit cleaning (by posing) from the adult-colored L. phthirophagus, indicating that
some hosts prefer the adult color pattern. Small L. phthirophagus shifted to adult
coloration more quickly when starved than when provided with host fish on which to
feed, indicating that the coloration shift is motivated by hunger. Even though juvenile coloration in some fishes may reduce the aggression
received from adults, in cleaner wrasses it also reduces food availability, making it
advantageous for them to shift to adult-coloration as soon as possible. Cleaner wrasses
have developed a quick, reversible coloration shift that allows changing to adult
coloration at a small size but allows reversing coloration if too much aggression is
received.
x, 59 leaves, bound : ill., maps ; 29 cm.
</description>
<pubDate>Tue, 01 Dec 1998 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/18159</guid>
<dc:date>1998-12-01T00:00:00Z</dc:date>
<dc:creator>Mahon, Jeffrey L</dc:creator>
</item>
<item>
<title>The ecology of patch reef fishes in a subtropical Pacific atoll: recruitment variability, community structure and effects of fishing predators</title>
<link>http://hdl.handle.net/10125/18158</link>
<description>The ecology of patch reef fishes was studied to quantify the main
factors that affect the natural variability of the fish community and
to determine the effects produced on the community by experimental
removal of predators. Initially, a year-long baseline description was
completed of the physical, biological and ecological characteristics of
8 pristine patch reefs at Midway lagoon. For over 3 subsequent years,
piscivorous predators were spearfished at least monthly, often for days
at a time, on 4 of the 8 reefs. Fish populations were visually
censused throughout the experiment. In all seasons and years of the
project, daily recruitment rate of postlarval fishes to natural patch
reefs was compared to that measured on standardized, artificial reefs
of various sizes and degrees of inter-reef isolation. Finally, all
baseline measurements were replicated and complete collections were
made of all fishes, to validate the visual census method.
Visual censusing was found to be of adequate precision and accuracy
for most resident, non-cryptic species (highest for small patch reefs).
Fishes could be assigned to size classes underwater by visual estimate
with high accuracy. Rotenone collections were highly effective in
quantifying many species commonly missed or underestimated in visual
censuses.
Only a few species composed the bulk of all recruits, while most
species were rare or not seen at all. Variation between species was
related to life history strategies or behavioral requirements. High temporal variability was found at the following scales: 1) Annuallywhere
variability increased with the magnitude of recruitment, and
different species recruited heavily in different years, suggesting that
species specific factors in the plankton are more important than
general oceanographic conditions; 2) Seasonally- pulsing strongly in
summer, and occasionally late fall, when favorable environmental
conditions may maximize growth and survival; and 3) Daily- with 1 or 2
strong peaks (each only a few days long) over a period of several weeks
of low, variable recruitment.
Small-scale spatial variability between replicate attractors
(standardized artificial reefs) and between attractor types (coral and
wire) were both high for a few species recruiting abundantly, although
most recruits are probably substrate generalists. Rigorous visual fish
censuses can adequately document moderate- to long-term temporal
variation in the abundances of recently recruited juveniles on patch
reefs (i.e., based on similar temporal patterns assessed by daily
attractors). Daily total recruitment rate increased, although at
diminishing densities, with (attractor) reef size, and with degree of
inter-reef isolation. Abundances of recently recruited fish censused
on neighboring, natural patch reefs (much larger than attractors)
increased with reef size. The effect of isolation on these natural
reefs was confounded by the stronger effect of reef size. These
results suggest that if optimum size and spacing of reefs is provided,
either by proper design of artificial reefs or selection of marine reserves, managers may enhance fish recruitment and ultimately improve
local fisheries:
Of the 135 fishes censused on the patch reefs studied, only 6
species together accounted for 70% of the total number of all fish,
mainly due to heavy seasonal recruitment pulses. Strong seasonal and
annual variability in recruitment was responsible for most of the
temporal variation in fish abundance. The structure of patch reef fish
communities at Midway was characterized by high unpredictability (e.g.,
great seasonal and/or annual variability in recruitment by common
species, recruitment limitation for most species, and a high turnover
rate detected by frequent sampling). Some predictions of the theory of
island biogeography were also met by these fish communities (e.g.,
species richness correlated strongly with patch reef area, volume and
relief). and total fish abundance. Some populations also exhibited a
degree of long-term stability. Species diversity [H'] was similar
among different size reefs.
The experimental fishing on piscivores produced a catch composed
mainly of lizardfish, due largely to immigration following the removal
of other, competitively superior, highly resident piscivores.
Scorpionfish and moray eels were also dominant predators. The expected
decreases in catch-per-unit-effort were not realized, except for a
quantitatively insignificant family (hawkfish). Conversely, the catch
of the highly migratory lizardfish actually increased as fishing
progressed. Changes in the catch composition for other piscivores related mainly to major changes in reef size or to patterns of large,
inter-year recruitment fluctuations. Census data confirmed the major
trends indicted by catch results. Sharks and jacks were attracted to
the experimental reefs by spearfishing; the study was unable to
determine whether their piscivorous effect was different between reef
treatments.
Patch reef fish communities at Midway were relatively resilient to
long-term, intense fishing pressure on piscivores. However, enhanced
survival of a large, annual, summer recruitment pulse of a common
cardinalfish, synchronized with a temporary but significant reduction
of lizardfish (the most prevalent piscivore) by fishing, suggested that
an effect of predation on reef fish populations is experimentally
detectable and considerable. However, temporal and spatial variability
in recruitment, and reef size differences and changes in size were the
primary factors responsible for the observed temporal patterns in fish
abundance. COlnmunity analysis involves numerous confounding effects
and requires the most careful interpretation for valid conclusions.
xvi, 321 leaves, bound : ill. ; 29 cm.
</description>
<pubDate>Mon, 01 May 1989 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/18158</guid>
<dc:date>1989-05-01T00:00:00Z</dc:date>
<dc:creator>Schroeder, Robert E</dc:creator>
</item>
<item>
<title>Growth, bioenergetics and life-span of Octopus cyanea and Octopus maya</title>
<link>http://hdl.handle.net/10125/18157</link>
<description>The objectives of the work undertaken were to: (1)
rear Octopus cyanea and Octopus maya through all stages of
the life cycle in the laboratory; (2) measure growth rates;
(3) determine energy budgets; (4) examine the effects of
temperature, size and age on food intake, growth, metabolism
and conversion efficiency; and (5) determine life-spans
of the two species.
Attempts to rear O. cyanea through the planktonic stage
were unsuccessful and data were obtained on feral animals in
the laboratory. O. maya was reared through four generations
from eggs collected at Campeche, Mexico.
Animals were fed ad libitum on living crabs. Weights
were recorded at I5-day intervals and food intake was quantified.
Dry matter, ash and caloric content of crab and O.
cyanea samples were determined.
Animals grew exponentially for the first third of their
benthic life, doubling their weight every 11-13 days at 22
- 27 degrees C. The exponential growth phase was followed by a period
of logarithmic growth which terminated at full sexual
maturity. Average maximum sizes attained by the two species
were comparable (3.2 kg for O. maya and 3.6 kg for O.
cyanea). O. cyanea settles from the plankton at an estimated
weight of 0.3 g and attains maximum size about 10.5
months later. O. maya hatched as benthic juveniles weighing 0.1 g and grew to maximum size in about 8.5 months. Maximum
size attained by both species varied from several hundred
grams to several kilograms depending on food availability.
Assimilation efficiency of O. cyanea was very high
(95%) and independent of animal size and food ration size.
Gross growth efficiency of both species averaged about
40% on a wet weight basis and was independent of size (old
animals excluded) and temperature. The relationship between
food intake and growth was linear in both species and showed
no sign of decrease at high ration level.
Material budgets indicated that on a wet weight basis,
40% of ingested food was used in growth, 55% in maintenance
and 5% was not absorbed. Energy budgets on a caloric basis
indicated that 60% of ingested energy was used in growth,
36% in total metabolism and 4% voided as feces.
Rates of food intake, growth and metabolism were about
twice as high at 30 as at 20 degrees C.
Females of both species died after brooding their eggs
and males died at about the same age. O. cyanea had a lifespan
of 12-15 months from settlement and O. maya lived an
average of 10 months from hatching in the laboratory.
Low light intensity and elevated temperature in the
laboratory were thought to produce early spawning and hence
short life-spans in laboratory animals. A theory is presented to explain large variations in
size at spawning and lack of seasonality. Growth, differentiation,
maturation and spawning are viewed as programmed
events in the life cycle. Light, temperature and food determine
the rate at which the program runs and hence size
and age at spawning. Senescence and death are viewed as
events occurring after the program is completed.
</description>
<pubDate>Sun, 01 Aug 1976 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/18157</guid>
<dc:date>1976-08-01T00:00:00Z</dc:date>
<dc:creator>Van Heukelem, William F</dc:creator>
</item>
<item>
<title>Responses of Hawaiian Scleractinian Corals to Different Levels of Terrestrial and Carbonate Sediment</title>
<link>http://hdl.handle.net/10125/15323</link>
<description>Goals of this investigation were: 1) Differentiate between the effects of&#13;
turbidity and sedimentation on corals. 2) Differentiate the effects of carbonate&#13;
and terrigenous sediments on coral growth and metabolism. 3) Develop a&#13;
predictive model relating increased sediment loading to the photosynthetic rate,&#13;
growth and survival of corals. 4) Evaluate the validity of the widely cited "10 mg&#13;
cut-off point" and determine the levels of turbidity and sedimentation that are&#13;
tolerated by corals. Earlier studies suggest that coral reefs decline when sediment loading levels exceed a sediment trapping rate of 10 mg cm-2 d-1 or a&#13;
turbidity of 10 mg I-1.&#13;
An integrated experimental design linked field and laboratory experiments.&#13;
In the field, corals were transplanted to sites with varying levels of sedimentation.&#13;
Turbidity, as linked to reduced light availability, had a significant affect on coral&#13;
growth and metabolism in laboratory experiments but not coral growth or survival&#13;
in field experiments. Turbidity in the field was highly variable and influenced&#13;
greatly by wind velocity and rainfall.&#13;
Terrigenous (or land-derived) sediments influenced light extinction more&#13;
than carbonate (reef-derived) sediments. In laboratory experiments turbidity was&#13;
more important than sediment trapping rate in affecting the photosynthetic ability&#13;
and growth rates of corals.&#13;
The predictive model stated that the lower the light level (as caused by&#13;
increased turbidity) the lower the photosynthetic production of corals. The model&#13;
was supported by results of laboratory experiments where conditions were precisely controlled and monitored. Under field conditions, the predictive model&#13;
did not hold due to extreme natural variability in sediment loading and variation in&#13;
a wide range of other environmental factors encountered at the experimental&#13;
sites.&#13;
Corals tolerated turbidity exceeding 120 mg I-1 and sediment trapping&#13;
rates in excess of 11 mg cm2 d-1. Sediment loading is correlated with other&#13;
environmental factors such as nutrient loading and reduced salinity. Composition&#13;
of sediment varies widely between different locations. The "10 mg cutoff may&#13;
prove to be useful in setting limits to vigorous coral reef development, although&#13;
individual corals or coral assemblages may be able to survive and grow at levels&#13;
exceeding this value.
Thesis (Ph. D.)--University of Hawaii at Manoa, 2001. Includes bibliographical references (leaves 235-264).
</description>
<pubDate>Tue, 01 May 2001 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/15323</guid>
<dc:date>2001-05-01T00:00:00Z</dc:date>
<dc:creator>Te, Franklyn Tan</dc:creator>
</item>
<item>
<title>Genotypic Diversity and Population Structure of the Hawaiian Reef Coral, Porites compressa</title>
<link>http://hdl.handle.net/10125/15322</link>
<description>The assessment of clonal diversity in populations of the endemic
Hawaiian coral Porites compressa was undertaken using four independent
assays of genotypic identity: colony morphology, immunocompatibility
testing by tissue grafting, electrophoresis of soluble proteins, and
chromatography of ultra-violet absorbing compounds. All methods were
corroborative, but electrophoresis of soluble proteins provided the
single most efficacious assay of genotypic diversity, with a 7-locus
(21 alleles) system which was estimated to sufficiently resolve approximately
95% of clonal samples.
Populations of Porites compressa were demonstrated to have
derived substantial contributions from both sexual and asexual modes of
reproduction. Sexual reproduction in P. compressa was similar in most
life history parameters to other Porites species that broadcast spawn.
Age at first reproduction was estimated to be between 1.8 and 2.5
years. Mean oocyte diameters were approxiInately 250 um at spawning,
with 10-30 eggs per polyp. Spawning was synchronized with full moon
during summer months, and some colonies spawned over more than one
night and over subsequent months. Planulae were competent to
metamorphose after three days, and sibling juveniles which settled
gregariously were often observed to fuse, suggesting that there may be
ontogenetic changes in self-recognition responses in this species.
Production of asexual propagules by fragmentation was calculated
to be between 35 and 96 fragments/m2/year for a patchreef population of
Porites compressa in Kaneohe Bay, Oahu. Fragment production was
continuous through the year, with a 5-10 fold increase in summer months due pertlaps to increased activity of turtles near sheltering areas on
the reef. Asexual propagules were large (1.5-151 cm2) and survived
for many weeks or months before "recruiting" or being lost from the
fragment pool.
Spatial and/or numeric abundance of dominant and rare clones of
Porites compressa could be explained, in part, by differences in
measurable fitness parameters of growth rate and competitive ability.
No significant differences in the propensity of clones to produce
fragments were detected. The relationship between clonal abundance and
single fitness correlates, however, was not a simple one. Clonal
fitness is the sum of many life history and ecological characteristics
of a genotype. Clonal abundance and distribution may also be effected
by non-selective random physical processes leading to asexual colony
replication and recruitment.
Genotypic diversity in six populations of Porites compressa was
directly related to habitat disturbance histories. Highest diversity
was found in populations which had been intensely or recently disturbed. In these populations, space was not limited and mean colony
size was small (&lt;500 cm2), suggesting an early stage in population
recolonization. In a stable, undisturbed population, low genotypic
diversity revealed the extent of clonal replication of established
genotypes. Unoccupied substratum was rare in this habitat, and
average colony size was larger (&gt;2000 cm2). Single clones were
distributed over small or large areas (&lt;1 to &gt;16 m2) or distances (&lt;1
to &gt;90 m), and were numerically (&gt;13% of total number of colonies) or
spatially (&gt;15% of total colony area) dominant.
Typescript. Thesis (Ph. D.)--University of Hawaii at Manoa, 1988. Includes bibliographical references.
</description>
<pubDate>Thu, 01 Dec 1988 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/15322</guid>
<dc:date>1988-12-01T00:00:00Z</dc:date>
<dc:creator>Hunter, Cynthia L</dc:creator>
</item>
<item>
<title>The Ecology of Juvenile Hawaiian Corals</title>
<link>http://hdl.handle.net/10125/15320</link>
<description>I studied coral recruitment, growth and community&#13;
development in Kaneohe Bay, Oahu, Hawaii. In one&#13;
experiment, I investigated coral recruitment at 7 sites, in&#13;
3 consecutive years. Coral community development was&#13;
followed for up to 3 y. Hollow concrete blocks were used&#13;
as experimental substrata. The smallest recruits which I&#13;
detected were 1 mm in diameter.&#13;
variability in recruitment was observed both between&#13;
sites and between surfaces of the blocks. Temporal&#13;
variability in recruitment patterns between years was also&#13;
recorded. After 3 mo immersion, Pocillopora damicornis, a&#13;
brooding species, was-the most abundant coral. Another&#13;
brooding species, Cyphastrea ocellina, and the ahermatype,&#13;
Culicia cf. tenella were also detected. Two spawning.&#13;
species, Montipora verrucosa and Porites compressa were not&#13;
detected until after 6 mo immersion. Over 3 y, the&#13;
relative abundance of Pocillopora damicornis declined at&#13;
most sites and the relative abundance of Porites compressa&#13;
increased. Montipora verrucosa recruits remained uncommon.&#13;
The distribution of hermatypic corals on the blocks&#13;
also changed with time. Initially recruits were most&#13;
abundant on interior top surfaces after 3 y, they were most&#13;
common on outer surfaces of the blocks.&#13;
Inter- and intraspecific differences in growth were&#13;
recorded. pocillopora damicornis attained the largest colony sizes. Growth rates varied considerably between&#13;
sites. Successful recruitment was highest after 3 y&#13;
immersion, at sites where corals grew most rapidly.&#13;
In the second set of experiments, I measured invisible&#13;
recruitment sensu wallace (1983) and investigated the&#13;
effects of urchin and fish grazing on coral recruitment.&#13;
Montipora verrucosa was the most common recruit after 3 mo&#13;
immersion. Fish and urchin grazing significantly affected&#13;
the abundance of M. verrucosa but not that of Porites&#13;
compressa or Pocillopora damicornis.&#13;
After 3 mo immersion, the maximum size attained by P.&#13;
damicornis was greater than P. compressa or M. verrucosa&#13;
which had similar colony diameters and number of polyps.&#13;
However, during the next 5 mo P. compressa grew more&#13;
rapidly than M. verrucosa. The different growth rates of&#13;
these species explains why P. compressa increased, and M.&#13;
verrucosa decreased in relative abundance.&#13;
Interspecific differences in larval size at&#13;
settlement, the time taken to deposit a skeleton, and postsettlement&#13;
growth strategies, all influence recruitment&#13;
success.
Thesis (Ph. D.)--University of Hawaii at Manoa, 1993. Includes bibliographical references (leaves 240-252)
</description>
<pubDate>Sat, 01 May 1993 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/15320</guid>
<dc:date>1993-05-01T00:00:00Z</dc:date>
<dc:creator>Fitzhardinge, Rachel C</dc:creator>
</item>
<item>
<title>Studies in the mineral metabolism of the Hawaiian crab, Podophthalmus vigil (Fab.) throughout the ecdysis cycle</title>
<link>http://hdl.handle.net/10125/12022</link>
<description>Typescript.; Thesis (Ph. D.)--University of Hawaii, 1965.; Bibliography: leaves 138-147.; vii, 147 l mounted illus., tables
</description>
<pubDate>Fri, 01 Jan 1965 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12022</guid>
<dc:date>1965-01-01T00:00:00Z</dc:date>
<dc:creator>Sather, Bryant Thomas</dc:creator>
</item>
<item>
<title>The venom from the heads of the globiferous pedicellariae of the sea urchin, Tripneustes gratilla (Linnaeus)</title>
<link>http://hdl.handle.net/10125/12021</link>
<description>Typescript.; Thesis--University of Hawaii, 1964.; Bibliography: leaves 124-126.; xiii, 126 leaves ill. (part mounted, part col.), tables
</description>
<pubDate>Wed, 01 Jan 1964 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12021</guid>
<dc:date>1964-01-01T00:00:00Z</dc:date>
<dc:creator>Alender, Charles Baker</dc:creator>
</item>
<item>
<title>Life history and behavior of Dascyllus albisella Gill, a pomacentrid reef fish</title>
<link>http://hdl.handle.net/10125/12020</link>
<description>Typescript.; Thesis--University of Hawaii, 1963.; Bibliography: leaves 214-221.; viii, 221 leaves mount. ill., diagrs., tables
</description>
<pubDate>Tue, 01 Jan 1963 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12020</guid>
<dc:date>1963-01-01T00:00:00Z</dc:date>
<dc:creator>Stevenson, Robert Alexander</dc:creator>
</item>
<item>
<title>Uptake and release of phosphorus by representatives of a coastal marine ecosystem</title>
<link>http://hdl.handle.net/10125/12019</link>
<description>Typescript.; Thesis--University of Hawaii, 1963.; Bibliography: leaves [80]-86.; iii, 86 leaves mount. illus., diagrs. (part fold.) tables
</description>
<pubDate>Tue, 01 Jan 1963 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12019</guid>
<dc:date>1963-01-01T00:00:00Z</dc:date>
<dc:creator>Johannes, R. E (Robert Earle), 1936-2002</dc:creator>
</item>
<item>
<title>A contribution to the biology of caligoid copepods parasitic on acanthurid fishes of the Hawaiian Islands</title>
<link>http://hdl.handle.net/10125/12018</link>
<description>Typescript.; Thesis (Ph. D.)--University of Hawaii, 1961.; Bibliography: leaves [453]-471.; xii, 471 l illus. (part mounted) diagrs., tables
</description>
<pubDate>Sun, 01 Jan 1961 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12018</guid>
<dc:date>1961-01-01T00:00:00Z</dc:date>
<dc:creator>Lewis, Alan Graham</dc:creator>
</item>
<item>
<title>Studies on the sea urchin egg nucleus: its isolation, structure, physical properties and DNA content</title>
<link>http://hdl.handle.net/10125/12017</link>
<description>Typescript.; Thesis (Ph. D.)--University of Hawaii, 1961.; Bibliography: leaves [118]-123.; v, 123 leaves ill., map, diagrs
</description>
<pubDate>Sun, 01 Jan 1961 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12017</guid>
<dc:date>1961-01-01T00:00:00Z</dc:date>
<dc:creator>Hinegardner, Ralph T</dc:creator>
</item>
<item>
<title>Transport of lysine across the intestine of the freshwater prawn, Macrobrachium rosenbergii</title>
<link>http://hdl.handle.net/10125/12013</link>
<description>Typescript.; Bibliography: leaves 117-126.; viii, 126 leaves ill
</description>
<pubDate>Wed, 01 Jan 1975 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12013</guid>
<dc:date>1975-01-01T00:00:00Z</dc:date>
<dc:creator>Brick, Robert W</dc:creator>
</item>
<item>
<title>Planktonic prosobranch veligers of Kaneohe Bay</title>
<link>http://hdl.handle.net/10125/12012</link>
<description>Typescript.; Bibliography: leaves 563-582.; xiii, 593 leaves ill. (some col.), map
</description>
<pubDate>Wed, 01 Jan 1975 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12012</guid>
<dc:date>1975-01-01T00:00:00Z</dc:date>
<dc:creator>Taylor, Jane Bartlett</dc:creator>
</item>
<item>
<title>Sound localization in the bottlenose porpoise, Tursiops truncatus (Montagu)</title>
<link>http://hdl.handle.net/10125/12011</link>
<description>Typescript.; Bibliography: leaves 177-187.; xi, 187 leaves ill. (some col.)
</description>
<pubDate>Tue, 01 Jan 1974 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12011</guid>
<dc:date>1974-01-01T00:00:00Z</dc:date>
<dc:creator>Renaud, Donna McDonald</dc:creator>
</item>
<item>
<title>Aspects of the dynamics of mercury cycling in a small Hawaiian estuary</title>
<link>http://hdl.handle.net/10125/12010</link>
<description>Typescript.; Bibliography: leaves [201]-210.; xv, 210 leaves ill
</description>
<pubDate>Tue, 01 Jan 1974 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12010</guid>
<dc:date>1974-01-01T00:00:00Z</dc:date>
<dc:creator>Luoma, Samuel N</dc:creator>
</item>
<item>
<title>An analysis of metamorphosis in Phestilla sibogae Bergh 1905 (Gastropoda, Nudibranchia)</title>
<link>http://hdl.handle.net/10125/12009</link>
<description>Typescript.; Bibliography: leaves 219-234.; x, 234 l illus
</description>
<pubDate>Mon, 01 Jan 1973 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12009</guid>
<dc:date>1973-01-01T00:00:00Z</dc:date>
<dc:creator>Bonar, Dale Brian</dc:creator>
</item>
<item>
<title>Alizarin deposition by corals</title>
<link>http://hdl.handle.net/10125/12008</link>
<description>Typescript.; Bibliography: leaves 155-163.; xi, 163 l illus. (part col.), tables
</description>
<pubDate>Mon, 01 Jan 1973 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10125/12008</guid>
<dc:date>1973-01-01T00:00:00Z</dc:date>
<dc:creator>Lamberts, Austin E</dc:creator>
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