Research
Selected Research Articles 2001Present
(Click here for
selected research articles 19982000)
Below are abstracts of Rhode Island Sea Grantfunded
research articles. To order a copy of the article, contact
Rhode Island Sea Grant Communications at (401) 874-6842.
The National
Sea Grant Library is the official Sea Grant archive. Library
staff lend documents all over the world and maintain a searchable
bibliographic database where you may obtain citations and
abstracts of Sea Grant publications and, in many cases, a
full text copy of the document.
Topics:
Coastal Ecosystems | Ecosystem
Modeling | Eelgrass | Fishing
Gear | Invasive Species | Lobster
| Nutrients | Oyster
| Salt Marshes| Summer
Flounder | Ecolabeling
Coastal Ecosystems
Nixon, S. W. 2003. Replacing the Nile:
Are anthropogenic nutrients providing the fertility once brought
to the Mediterranean by a great river? Ambio 32(1):30-39.
RIU-W-03-001 (P1653); 10pp.; $3.00.
The Nile River fertilized the Mediterranean
Sea off the coast of Egypt until the high dam at Aswan was
closed in 1965. Afterwards, the local fisheries collapsed,
but began a dramatic recovery in the 1980s, coinciding with
human population growth and development. Calculations indicate
that human sewage and agricultural drainage may now support
the fertility once provided by the Nile.
Nixon, S.W. et al. 2004. A one-hundred-and-seventeen-year
coastal water temperature record from Woods Hole, Massachusetts.
Estuaries 27(3):397-404.
RIU-R-04-002 (P1704); 8 pp.; $3.00.
Near-surface water temperature measurements
have been made almost daily at Great Harbor, Woods Hole, Mass.,
since 1886, perhaps the longest coherent sea surface temperature
record in North America. Trends observed included cooling
during the 1960s after no significant trend for the first
60 years of observation. Significant warming occurred from
1970 through 2002.
Ecosystem Modeling
Brush, M.J. et al., 2002. Modeling phytoplankton
production: Problems with the Eppley curve and an empirical
alternative. Marine Ecology Progress Series 238:31-45.
RIU-R-02-004 (P1645); 15pp.; $3.00.
The discrepancy between measured and modeled
rates of primary production, together with the importance
of accurately predicting such rates, has led the authors to
examine the traditional way in which phytoplankton growth
and primary production are formulated in aquatic simulation
models, and in particular the Eppley curve. The authors have
searched the literature for evidence of culture studies that
violate the curve, and have compared growth rates measured
in situ to those predicted by the Eppley curve from two
estuaries (Narragansett Bay, R.I., and Waquoit Bay, Mass.)
and two mesocosm facilities at the University of Rhode Island.
An empirical alternative to the Eppley curve is presented
and examined for its potential application in estuarine simulation
models.
Sullivan, B. and C. Kincaid,. 2001. Modeling
circulation and transport in Narragansett Bay. EOS Suppl.
82(2):S216.
Eelgrass
Brush, M.J. and S.W. Nixon, 2002. Direct
measurements of light attenuation by epiphytes on eelgrass
Zostera marina. Marine Ecology Progress Series 238:73-79.
RIU-R-02-002 (P1640); 7pp.; $3.00.
Declines in the eelgrass Zostera marina
in estuaries and lagoons have been attributed in part to reductions
in irradiance reaching the grass blades. Epiphytes growing
on Z. marina have the potential to attenuate a large
fraction of the light that would otherwise reach the blades.
In this study, scientists measured light penetration across
a wide range of epiphytic densities by holding scraped and
unscraped Z. marina blades over a submerged light sensor.
Results indicate this method may be more accurate than those
in previous studies.
Harris, L.A. et
al., 2004. Experimental studies of predation by bluefish Pomatomus
saltatrix in varying densities of seagrass and macroalgae.
Marine Ecology Progress Series 281:233-239.
RIU-R-04-003 (P1718); 7pp.; $3.00.
Researchers conducted ecosystem-level experiments
to investigate predator-prey relationships in three habitat
types: eelgrass Zostera marina, macroalgae, and bare sediment.
Specially designed mesocosms containing marine sediments,
coastal water, and varying densities of eelgrass or macroalgae
were used to simulate conditions found in shallow coastal
lagoons of Rhode Island. Bluefish were used as predators in
each experiment. Eelgrass significantly increased the survivorship
of silversides, tautog, and cunner at very low shoot densities.
Experiments using macroalgae did not result in significantly
different survival rates between bare sand and macroalgae
habitat for silversides or cunner, the two species tested
for this vegetation type.
Nixon, S.W. et al., 2001. Responses of
very shallow marine ecosystems to nutrient enrichment. Human
and Ecological Risk Assessment 7(5):1457-1481.
RIU-R-01-005 (P1629); 25pp.; $3.00.
The authors have not been able to find useful
relationships between nutrient input and the type of plant
providing most of the primary production or between nutrient
input and the amount of primary production in shallow lagoon
ecosystems. However, total system production does increase
with nutrient enrichment at very low rates of input, and eelgrass
does not persist when exposed to even moderate levels of fertilization.
Eelgrass responds to inorganic nitrogen enrichment and to
shading by increasing the rate of leaf elongation and decreasing
the allocation of resources to below-ground roots and rhizomes.
This reduces or eliminates lateral branching of the rhizomes
and causes a decline in the density of shoots. Based on mesocosm
studies, the authors propose several indicators of eelgrass
health, including the rate of leaf elongation, plant density,
and the shoot:root biomass ratio.
Essential Fish Habitat
DeLong, A.K. and J.S. Collie, 2004. Defining
Essential Fish Habitat: A Model-Based Approach. Rhode Island
Sea Grant, Narragansett, R.I. RIU-T-04-002 (P1695); 4 pp.
This booklet describes an improvement on the
method of defining essential fish habitat that currently designates
most of the species' range as "essential." This
new approach can be used to obtain smooth and continuous regions
representing any desired population percentile. Available
as pdf.
Fishing Gear
National Research Council, 2002. Effects
of Trawling and Dredging on Seafloor Habitat. National
Academy Press, Washington, D.C. 126pp.
Invasive Species
Casagrande, R.S. 2003. Rhizedra lutosa,
a natural enemy of Phragmites australis in North America.
Estuaries 26(2B):602-606.
RIU-R-03-007 (P1697); 5pp; $3.00.
Rhizedra lutosa, an insect native to
Europe and now found in North America, has been reported to
cause serious damage to Phragmites australis in the
Netherlands. Researchers are investigating the moth as part
of an effort to characterize natural enemies of P. australis
toward a goal of biological control of this invasive plant.
They found that R. lutosa larvae feed on stems and
rhizomes of P. australis growing in dry sites. They
determined that the insect does cause a reduction of plant
growth in some sites; however, because of low moth densities,
this effect is small.
Costa-Pierce, B.A. 2003. Rapid evolution
of an established feral tilapia (Oreochromis spp.):
The need to incorporate invasion science into regulatory structures.
Biological Invasions 5: 71-74.
The hybridization of cultivated and native tilapia
has made regulating exotic tilapia species difficult. This
paper recommends that a system of ecotypes (code names) based
on DNA markers be developed to label and regulate feral tilapia
strains, and that hybrid strains be collected into a registry
of species based on DNA markers.
Lobster
Castro, K., et al. 2001. Habitat addition
and stock enhancement for American lobsters, Homarus americanus.
Marine and Freshwater Research 52(8):1253-1261.
Six experimental artificial reefs established
in Narragansett Bay in 1997 have been monitored, and results
show that juvenile and adult lobster density at the reef increased
significantly compared with control areas. Settlement of young-of-year
lobsters has significantly increased. The researchers used
microwire tags to mark hatchery-reared lobsters and released
over 2000 in each of two years. The density of young-of-year
lobsters on enhanced reefs was not different from that on
the control reefs. Only one hatchery-reared lobster was recovered.
Field observations indicate possible behavior differences
in hatchery-reared lobsters might make them more susceptible
to predation.
Saila, S.B. et al. 2002. Does lobster
trap bait influence the Main inshore trap fishery? North
American Journal of Fisheries Management 22: 602-605.
The purpose of this research is to determine
whether evidence indicates that bait may make an important
contribution to increases in lobster production.
Nutrients
Buckley, B.A. and S.W. Nixon, 2002. A
strikingly rich zoneNutrient enrichment and secondary
production in coastal marine ecosystems. Estuaries
25(4b):782-796.
RIU-R-02-003 (P1642); 15pp.; $3.00.
Unique multiple-year fertilization experiments
were carried out over 50 years ago in Scottish sea lochs that
showed dramatic increases in the abundance of benthic infauna
and greatly enhanced growth of fish as a result of inorganic
nitrogen (N) and phosphorus (P) additions. These experiments
appear to provide a good qualitative model for the responses
of the Baltic Sea to nutrient enrichment and resulting eutrophication.
The authors review the literature for both locations. They
also discuss the recent demonizing of N, and note that decisions
regarding the amount of N or P that will be allowed to enter
marine ecosystems should be made with the knowledge that there
may be tradeoffs between increases in water clarity and dissolved
oxygen and the abundance of fish, shellfish, and other desirable
animals.
McKenna, J.H. et al., 2001. Understanding
groundwater nitrogen and carbon dynamics along estuarine margins:
Insights and challenges. EOS Suppl. 82(2):S152.
Nixon, Scott et al., 2001. Responses
of very shallow marine ecosystems to nutrient enrichment.
Human and Ecological Risk Assessment, 7(5): 1457-1481, 2001.
RIU-R-01-005 (P1629); 25pp.
The authors have not been able to find useful
relationships between nutrient input and the type of plant
providing most of the primary production or between nutrient
input and the amount of primary production in such shallow
lagoon systems. However, total system production does increase
with nutrient enrichment at very low rates of input, and eelgrass
does not persist when exposed to even moderate levels of fertilization.
"Zostera" responds to inorganic nitrogen enrichment
and to shading by increasing the rate of leaf elongation and
decreasing the allocation of resources to below ground roots
and rhizomes. This reduces or eliminates lateral branching
of the rhizomes and causes a decline in the density of shoots.
Based on mesocosm studies, the authors propose several indicators
of eelgrass health, including the rate of leaf elongation,
plant density, and the shoot:root biomass ratio.
Oyster
Munoz, P. and M. Gomez-Chiarri, 2002.
Protease activity in the Eastern oyster, Crassostrea virginica,
after experimental infection with the protozoan parasite Perkinsus
marinus. J. Shellfish Res. 21(1):376.
Perkinsus marinus is responsible for
disease and mortality of the American oyster, Crassostrea
virginica. This study investigated the interactions between
P. marinus and oyster hemocytes by measuring protease
activity in plasma of oysters collected at intervals after
experimental infection with P. marinus. This study
provides insights into the role of proteases in the pathogenesis
of Dermo disease.
Salt Marshes
Bertness, M.D. et al., 2002. Anthropogenic
modification of New England salt marsh landscapes. Proceedings
of the National Academy of Science 9(3):1395-1398.
Donnelly, J. and M.D. Bertness, 2001.
Rapid shoreward encroachment of salt marsh vegetation in response
to sea level rise. Proceedings of the National Academy
of Science 98:14218-14223.
The distribution of New England salt marsh communities
is intrinsically linked to the magnitude, frequency, and duration
of tidal inundation. Cordgrass (Spartina alterniflora)
exclusively inhabits the frequently flooded lower elevations,
whereas a mosaic of marsh hay (Spartina patens), spike
grass (Distichlis spicata), and black rush (Juncus
gerardi) typically dominate higher elevations. This study
examined relationships among marsh vegetation populations,
climate warming, and sea-level rise.
Emery, N.C. et al., 2001. Competition
and salt-marsh plant zonation: Stress tolerators may be dominant
comeptitors. Ecology 82(9):2471-2485.
Summer Flounder
Gavlik, S. et al., 2002. Metamorphosis
in summer flounder: Manipulation of thyroid status to synchronize
settling behaviour, growth, and development. Aquaculture
203:359-373.
In the aquaculture of summer flounder, the inherent
variation in growth and settling behavior during metamorphosis
may lead to cannibalism and necessitate increased labor due
to grading. The reasearchers' goal was to use thyroid hormone
manipulation to synchronize settling behavior and produce
uniform juvenile flounder. The treatment given eliminated
the larger, potentially cannibalistic juveniles found in control
tanks. Percent survival was unaffected by treatment.
Ecolabeling
Johnston, R.J. et al., 2001. Measuring
consumer preferences for ecolabeled seafood: An international
comparison. Journal of Agricultural and Resource Economics
26(1): 20-39.
International seafood ecolabeling programs have
been proposed to create market-based incentives for fisheries
managers to promote sustainable fisheries. This study evaluates
factors that may influence consumers' acceptance of such a
program. Following a contingent-choice telephone survey of
random households in the United States and Norway, a wide
range of factors is found to influence consumers' likelihood
of purchasing ecolabeled seafood, including price premium,
species, consumer group, and certifying agency.
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