Bongiorni,
L., Shafir, S., Angel, D. and B. Rinkevich. 2003. Survival,
growth and gonad development of two hermatypic corals subjected
to in situ fish-farm nutrient enrichment. Marine Ecology
Progress Series 253:137-144.
In
this paper, the authors examined the impact on coral growth
and reproduction of fish farm effluent in the Gulf of Aqaba
(Eilat) in the Red Sea. The commonly held belief is that high
particulate and nutrient levels released by such operations
are damaging the corals on the local reefs. Indeed, it is generally
accepted that high nutrient levels can affect coral growth and
reproductive fitness. What is less commonly known is that as
the nature and concentrations of these nutrients vary, so do
their impacts on corals.
Two
study sites were selected, the Ardaq fish farm on the north
shore of the Gulf of Eilat where gilthead seabream are cultured
in sea pens and a more southern “pristine” reef
off the Inter-University Institute (IUI) of Eilat. The levels
of nitrite, nitrate and phosphate (micromolar) measured at the
two sites are listed in the table 1.
Table
1. Nutrient values at the Ardaq fish farm and the Inter-University
Institute (IUI) of Eilat.
Location
Ammonia
Nitrite
Nitrate
Orthophosphate
Fish
Farm
1.016
0.095
0.385
0.123
IUI
0.057
0.075
0.264
0.045
Forty
branches of Acropora eurystoma were removed from each
of ten different colonies located at the IUI. The resulting
400 pieces were mounted on to PVC plates, 200 were placed at
6 m depth on the reef at the IUI, and 200 were placed at 6 m
depth, 20-40 m from the fish cages within the middle of fish
farm. All fragments were stained with Alizarin red so that skeletal
growth could be later determined. After seven months, the fragments
were collected and measured for weight, linear extension of
branches and “ecological volume” (the water volume
occupied between the branches of the coral) and compared.
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In
another experiment, 190 small pieces of Stylophora pistillata
were glued onto PVC plates and placed at each location. Survival
rates and lateral growth were then measured at 3, 4 and 13 month
intervals.
In
addition, 14 colonies of similar sized Stylophora pistillata
growing at each of the two sites were sampled to assess
gonadal development. Finally, the lipid content of both species
of coral from both sites was examined.
The
result showed that Acropora grown at the fish farm
site had identical survival rates to those from the IUI site.
However, those from the fish farm exhibited a significant 3-fold
increase in weight and linear extension, and a significant 4-fold
increase in ecological volume compared to those at the IUI site.
The
fragments of Stylophora showed a similar trend with
those at the fish farm site showing significantly greater sizes
after 13 months. However, those at the IUI site showed greater
lateral growth rates, presumably due to the higher degree of
deposition and accumulation of particulate matter at the fish
farm site. Whereas the average growth rate of the IUI fragments
was high, those at the fish farm exhibited a gradual increase
in growth rate over time and eventually (after 13 months), those
colonies at the fish farm site were significantly larger than
those at the IUI site.
The
reproductive status of Stylophora was examined in 2001
at the beginning and peak of the reproductive season (January
and May 2001) and at the beginning of the 2002 (December 2001) reproductive season. The number of polyps with female gonads was higher at
the fish farm in January and May 2001, but in December, all
colonies at both sites had ovaries. The size of the oocytes
in colonies growing at the fish farm was larger but not significantly
so. However, the average number of oocytes per polyp was significantly
greater at the fish farm and there were significant differences
between seasons too with December 2001 having significantly greater
numbers than the previous season. The proportion of colonies
with male gonads was also greater at the fish farm site.
The
lipid content of naturally occurring colonies of Stylophora
at the fish farm site was significantly greater than at the
IUI site. However, there was no difference in the lipid content
of the Acropora used in the study after 7 months.
This
study tends to contradict earlier studies that showed detrimental
effects of increased nutrient levels on not only coral growth
but also coral reproductive state. Although various studies
have shown that elevated nutrient levels are generally associated
with detrimental effects on coral growth and reproduction it
has been proposed that the chemical form and concentration of
these nutrients may actually determine whether there is a positive
or negative effect. It is well known that corals will absorb
ammonium and use it to enhance growth. Nutrient types and concentrations
may very well dramatically determine the type of response exhibited
by reef organisms. While elevated nutrients are often cited
as major contributors to the decline of reef health, it is often
difficult to distinguish the effects of any one factor when
dealing with multiple impacts on reef health such as anthropogenic
pollution, human use (i.e. SCUBA), siltation, sand deposition
etc. Of course, the short term of this study may mask any long
term detrimental effects of elevated nutrient levels on coral
health as well.
For
aquarists the lessons are clear, the obsession with nutrients
such as ammonia, nitrate and phosphate may be slightly misplaced.
While it is generally advised that these nutrients be as low
as possible (0 is often quoted as the ideal for ammonia for
example), they may not be detrimental at certain concentrations
and it may actually be beneficial to have slightly elevated
levels of certain nutrients such as nitrogen to aid coral growth.
Of course, one must not loose sight of the fact that hobbyist
test kits are a far cry from being able to measure the levels
mentioned in this study and it is probably safe to assume that
the levels for many nutrients are still several times that of
oligotrophic reef waters.
At
this point, I would like to mention a pet “theory”
of mine. One of the widespread “fads” in reef keeping
today is the addition of phytoplankton cultures and other “foods”
to reef aquaria. Often these are fed to tanks containing predominantly
LPS corals in the belief that these coral will feed on this
food. Observations are often made that the corals look much
better and colorful after several weeks of such feedings. I
would like to propose the theory that the benefit may not be
so much from the actual ingestion of the food but the decomposition
of the food leading to the generation of nitrogenous wastes
which are then absorbed by the corals resulting in better pigmentation
and increased zooxanthellae populations.
Recent Publications
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A.P. and R.T. Bauer. 2003. Growth, survivorship, life-span and
sex change in the hermaphroditic shrimp Lysmata wurdemanni
(Decaopoda: Caridea: Hippolytidae). Marine Biology
143(1):157-166.
Cunha,
F., SaboridoRey, F. and M. Planas. 2003. Use of multivariate
analysis to assess the nutritional condition of fish larvae
from nucleic acids and protein content. Biological Bulletin
204(3):339-?.
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Curtis,
C.J. 2003. Culture of harpacticoid copepods: Potential as live
feed for rearing marine fish. Advances in Marine Biology,
vol. 44. Academic Press, 2003, 325 pp. ISBN 0-12-026144-8.
McCormick,
M.I. 2003. Consumption of coral propagules after mass spawning
enhances larval quality of damselfish through maternal effects.
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Pati,
A.C. and G. Belmonte. 2003. Disinfection efficacy on cyst viability
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Jantzen,
T.M. and J.N. Havenhead. 2003. Reproductive behavior in the
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204(3):290-304.
Jantzen,
T.M. and J.N. Havenhead. 2003. Reproductive behavior in the
squid Sepioteuthis australis from south Australia:
Interactions on the spawning grounds. Biological Bulletin
204(3):305-317.
Steer,
M.A., Moltshaniwskyj, N.A. and A.R. Jordan. 2003. Emryonic development
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Corals
Fine,
M. and Y. Loya. 2003. Alternate coral-bryozoan competitive superiority
during coral bleaching. Marine Biology 142(5):989-996.
Gateno,
D. and B. Rinkevich. 2003. Coral polyp budding is probably promoted
by a canalized ratio of two morphometric fields. Marine
Biology 142(5):971-974.
Kelmanson,
I.V. and M.V. Matz. 2003. Molecular basis and evolutionary origins
in color diversity in great star coral Montastraea cavernosa
(Scleractinia: Faviidae). Molecular Biology and Evolution
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Ojika,
M., Islam, M.K., Shintoni, T., Zhong, Y., Okamoto, T. and Y.
Sakagami. 2003. Three new cytotoxic acylspermidines from the
soft coral, Sinularia sp. Bioscience Biotechnology
and Biochemistry 67(6): 1410-1412.
Ribes,
M., Coma, R. and S. Rossi. 2003. Natural feeding of the temperate
asymbiotic octocoral-gorgonian Leptogorgia sarmentosa
(Cnidaria: Octocorallia). Marine Ecology Progressive
Series 254:141-150.
Sanchez,
J.A., McFadden, C.S., France, S.C. and H.R. Lasker. 2003. Molecular
phylogenetic analyses of shallow-water Caribbean octocorals.
Marine Biology 142(5):975-985.
Santos,
S.R., Gutiérez-Rodriquez, C., Lasker, H.R. and M.A. Coffroth.
2003. Symbiodinium sp. associations in the gorgonian
Pseudopterogorgia elisabethae in the Bahamas: high
levels of genetic variability and population structure in the
symbiotic dinoflagellates. Marine Biology 143(1):11-120.
Villinski,
J.T. 2003. Depth-dependant reproductive characteristics for
the Caribbean reef-building coral Montastraea faveolata.
Marine Biology 142(6):1043-1054.
Yacobovitch,
T., Weis, V.M. and Y. Benayahu. 2003. Development and survivorship
of zooxanthellate and azooanthellate primary polyps of the soft
coral Heteroxenia fuscescens: laboratory and field
comparisons. Marine Biology 142(6):1055-1064.
Freshwater Fish
Buhrnheim,
C.M. and C.C. Fernandes. 2003. Structure of fish assemblages
in Amazonian rain-forest streams. Copeia 2:255-262.
Hee,
H. 2003. Mystus impluriatus: A new species of bagrid
catfish (Teleostei: Bagridae) from eastern Borneo. Copeia
2:373-378.
Magurran,
A.E. and H.L. Queiroz. 2003. Partner choice in piranha shoals.
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Marine Fish
Asoh,
K. 2003. Gonadal development and infrequent sex change in a
population of the humbug damselfish, Dascyllus aruanus,
in continuous coral-cover habitat. Marine Biology 142(6):1207-1218.
Bush,
A. 2003. Diet and diel feeding periodicity of juvenile scalloped
hammerhead shakrs, Sphyrna lewini, in Kaneohe Bay,
Oahu, Hawaii. Environmental Biology of Fishes 67(1):1-12.
Bell,
E.M., Lockyear, J.F., McPherson, J.M., Marsden, A.D. and A.C.J.
Vincent. 2003. First field studies of an endangered South African
seahorse, Hippocampus capensis. Environmental
Biology of Fishes 67(1):35-46.
Cantermil,
D.P., Vaudo, J.J., Lowe, C.G., Whetherbee, B.M. and K.N. Holland.
2003. Diel movement patterns of the Hawaiian stingray, Dasyatis
lata: implications for ecological interactions between
sympatric species. Marine Biology 142(5):841-848.
Fangue,
N.A. and W.A. Bennett. 2003. Thermal tolerance responses of
laboratory-acclimated and seasonally acclimatized Atlantic stingray,
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Holbrook,
S.J. an R.J. Schmitt. 2003. Spatial and temporal variation in
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Holzman,
R. and A. Genin. 2003. Zooplanktivory by nocturnal coral-reef
fish: Effects of lights, flow and prey density. Limnology
and Oceanography 48(4):1367-1375.
Janse,
M. 2003. Considerations on the diet composition and feeding
rate of dermersal sharks in 15 Euopean public aquaria. Zoo
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Sponaugle,
S., Fortuna, J., Grorud, K. and T. Lee. 2003. Dynamics of larval
fish assemblages over a shallow coral reef in the Florida Keys.
Marine Biology 143(1):175-190.
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Miscellaneous
Baums,
I.B., Millers, M.W. and A.M. Szmant. 2003. Ecology of a corallivorous
gastropod Coralliophila abbreviata, on two scleractinia
hosts. I. Population structure of snails and corals. Marine
Biology 142(6):1083-1092.
Baums,
I.B., Millers, M.W. and A.M. Szmant. 2003. Ecology of a corallivorous
gastropod Coralliophila abbreviata, on two scleractinia
hosts. II. Feeding, respiration and growth. Marine Biology
142(6):1093-1102.
Chisholm,
R. 2003. Primary productivity of reef-building crustose coralline
algae. Limnology and Oceanography 48(4):1376-1387.
Connelly,
J.D. 2003. The monopolization of understory habitat by subtidal
encrusting coralline algae: a test of the combined efforts of
canopy mediated light and sedimentation. Marine Biology
142(6):1065-1072.
Estes,
A.M., Kempf, J.C. and R.P. Henry. 2003. Localization and quantification
of carbonic anhydrase activity in the symbiotic scyphozoan Cassiopea
xamachana. Biological Bulletin 204(3):278-289.
Griffin,
S.P., Garcia, R.P. and E. Weil. 2003. Bioerosion in coral reef
communities in southwest Puerto Rico by the sea urchin Echinometra
viridis. Marine Biology 143(1):79-84.
Larkum,
A.W.D., Koch, E.M.W. and M. Kühl. 2003. Diffusive boundary
layers and photosynthesis of the epilithic algal communities
of coral reefs. Marine Biology 142(6):1073-1082.
Leichter,
J., Stewart, H.L. and S.L. Miller. 2003. Episodic nutrient transport
to Florida coral reefs. Limnology and Oceanography 48(4):1394-1407.
Masunaga,
G. and H. Ota. 2003. Growth, reproduction of the sea snake,
Emydocephalus ijimae, in the central Ryukus, Japan:
a mark and recapture study. Zoological Science 20(4):461-470.
SanMartin,
G. and E. Nishi. 2003. A new species of Alcyonosyllis
Glasby and Watson, 2001 (Polychaete: Syllidae: Syllinae) from
Shimoda, Japan, commensal with the gorgonian Melithaea flabellifera.
Zoological Science 20(3):371-376.
Sousa,
W.P., Kennedy, P.G. and B.J. Mitchell. 2003. Propagule size
and predispersal damage by insects affect establishment and
early growth of mangrove seedlings. Oecologia 135(4):564-575.
Water Treatment
Losso,
J.N., Marshall, W.E., Rao, R.M. amd R.J. Portier. 2003. Adsorption
of metal ions by pecan shell-based granular activated carbons.
Bioresource Technology 89(2):115-120.