Marine Resources Assessment for the Marianas Operating ... - SPREP
Marine Resources Assessment for the Marianas Operating ... - SPREP
Marine Resources Assessment for the Marianas Operating ... - SPREP
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AUGUST 2005 FINAL REPORT<br />
The NEC, which provides <strong>the</strong> bulk of water passing <strong>the</strong> Mariana archipelago, is composed primarily of<br />
plankton-poor water. Detailed in<strong>for</strong>mation on <strong>the</strong> oceanic zooplankton community in <strong>the</strong> waters of <strong>the</strong><br />
<strong>Marianas</strong> MRA study area is practically nonexistent (Uchida 1983). Ra<strong>the</strong>r, data ga<strong>the</strong>red in waters<br />
surrounding <strong>the</strong> study area must be explored to gain insight into <strong>the</strong> zooplankton communities within <strong>the</strong><br />
study area. Total zooplankton biomass at <strong>the</strong> surface examined <strong>for</strong> <strong>the</strong> western Pacific and adjacent seas<br />
found that zooplankton biomass was <strong>the</strong> lowest within <strong>the</strong> NEC, reaching concentrations of only 1.35<br />
grams (g) wet weight/m 2 (Vinogradov and Parin 1973). Vinogradov and Parin (1973) also surveyed<br />
zooplankton biomass in <strong>the</strong> tropical Pacific, and at <strong>the</strong>ir station nearest <strong>the</strong> study area (13°31’N,<br />
139°58’E), zooplankton biomass was very low (11.7 mg/m 3 ).<br />
Studies on <strong>the</strong> neritic plankton have centered around Apra Harbor and Piti Reef on Guam. However, <strong>the</strong><br />
majority of studies have been per<strong>for</strong>med in conjunction with more general environmental surveys, and<br />
thus no long-term surveys have been conducted. In general, abundance of zooplankton is highly variable<br />
with respect to location and time (both throughout <strong>the</strong> day and month to month) (Uchida 1983). In Apra<br />
Harbor, <strong>the</strong> commercial port contains <strong>the</strong> highest levels of zooplankton abundance and is dominated by<br />
copepods (Uchida 1983). O<strong>the</strong>r organisms in <strong>the</strong> harbor include fish larvae, decapod zoeae (freeswimming<br />
larvae), and pteropods (Uchida 1983). In Tanapag Harbor, Saipan, <strong>the</strong> diurnal zooplankton<br />
community is dominated by copepods and <strong>the</strong> nocturnal zooplankton community by larval crustaceans<br />
(Uchida 1983).<br />
2.6 BENTHIC HABITATS<br />
Deep sea benthic habitats include seamounts, hydro<strong>the</strong>rmal vents, <strong>the</strong> abyssal plain, and trenches. The<br />
bottom sediments covering <strong>the</strong> sea floor in much of <strong>the</strong> study area are volcanic or marine in nature<br />
(Eldredge 1983). In <strong>the</strong> <strong>Marianas</strong> Trench, <strong>the</strong> seabed is composed mostly of sand and clays (Ogawa et<br />
al. 1997). Sediments found on <strong>the</strong> narrow shelves along <strong>the</strong> <strong>Marianas</strong> archipelago are a combination of<br />
volcanic and calcareous sediments derived from calcareous animal skeletons (Eldredge 1983).<br />
2.6.1 Seamounts<br />
Seamounts are undersea mountains that rise steeply from <strong>the</strong> ocean floor to an altitude greater than<br />
1,000 m above <strong>the</strong> ocean basin (Thurman 1997). Generally, seamounts tend to be conical in shape and<br />
volcanic in origin, although some seamounts are <strong>for</strong>med by tectonic movement and converging plates<br />
(Rogers 1994). The study area contains seamounts of both types. The seamount topography is a striking<br />
difference to <strong>the</strong> surrounding flat, sediment covered abyssal plain, and <strong>the</strong> effects seamounts can impart<br />
on local ocean circulation are complex and poorly understood (Rogers 1994). However, around<br />
seamounts increased levels of phytoplankton, primary production, and pelagic and demersal fish (Zaika<br />
and Kovalev 1984; Fedorov and Chistikov 1985; Greze and Kovalev 1985; Parin et al. 1985; Rogers<br />
1994) are correlated with current pattern alterations and Taylor columns (circulation vortices) (Darnitsky<br />
1980; Boehlert and Genin 1987; Rogers 1994).<br />
The large ranges in depth, hard substrate, steep vertical gradients, cryptic topography, variable currents,<br />
clear oceanic waters, and geographic isolation all combine to make seamounts a unique habitat <strong>for</strong> both<br />
deep-sea and shallow water organisms (Rogers 1994). Thus, seamounts are capable of supporting a<br />
wide range of organisms (Wilson and Kaufman 1987). To date, Richer de Forges et al. (2000) conducted<br />
<strong>the</strong> most extensive species identification on seamounts. Richer de Forges et al. (2000) found a range of<br />
108 to 516 species of fish and macro-invertebrates from three areas of seamounts in <strong>the</strong> southwest<br />
Pacific (Tasman Sea, Coral Sea). Approximately one third of species found were new to science and<br />
potentially endemic. The number of species encountered versus <strong>the</strong> sampling ef<strong>for</strong>t showed that more<br />
species are probably present on <strong>the</strong> seamounts <strong>the</strong>y investigated. Richer de Forges et al. (2000) noted<br />
that <strong>the</strong>re were significant differences in <strong>the</strong> species composition between groups of seamounts found at<br />
a same latitude and approximately 1,000 km apart. Such differences in seamount communities suggest<br />
that species dispersal is limited to clustered seamounts and that seamount species have localized<br />
distributions (Richer de Forges et al. 2000).<br />
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