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 />
nutrient rich layer (Rodier and LeBorgne 1997). As such, standing stocks of phytoplankton biomass<br />
(Radenac and Rodier 1996) and concentrations of chl a are low throughout <strong>the</strong> study area (less than 0.1<br />
mg per cubic meter [m 3 ]) (NASA 1998; Figure 2-6). In regions in which overall nutrient concentrations are<br />
low, <strong>the</strong> phytoplankton communities are dominated by small nanoplankton and picoplankton (Le Bouteiller<br />
et al. 1992; Higgins and Mackey 2000). This is true <strong>for</strong> <strong>the</strong> study area, as phytoplankton communities in<br />
<strong>the</strong> western Pacific are dominated by cyanobacteria (Synechococcus spp.), prochlorophytes,<br />
haptophytes, and chlorophytes (Higgins and Mackey 2000). These cells are less than one micron (µm) in<br />
size and comprise 60% of <strong>the</strong> total chl a measured (Le Bouteiller et al. 1992).<br />
Two regions of enhanced chl a (up to 0.06 mg/m 3 ) can be identified in <strong>the</strong> study area off <strong>the</strong> southwest<br />
coast of Guam and in <strong>the</strong> region surrounding <strong>the</strong> islands of Tinian and Saipan (Figure 2-6). These<br />
regions of enhanced chl a persist through both <strong>the</strong> rainy and dry seasons, with higher chl a<br />
concentrations occurring during <strong>the</strong> rainy season. Reasons <strong>for</strong> <strong>the</strong>se regions of higher chl a levels are not<br />
completely understood but may be a product of <strong>the</strong> island mass interacting with currents. This island<br />
mass effect has been previously observed <strong>for</strong> o<strong>the</strong>r islands located in oligotrophic or stratified regions<br />
including <strong>the</strong> Scilly Isles in <strong>the</strong> Celtic Sea (Simpson et al 1982), <strong>the</strong> Marquesas islands (Martinez and<br />
Maamaatuaiahutapu 2004), and <strong>the</strong> islands of Hawai’i (Gilmartin and Revelante 1974) in which currents<br />
passing by <strong>the</strong> islands or through channels in island chains created turbulence mixing bringing more<br />
nutrient rich waters to <strong>the</strong> surface. This mixing may be capable of occurring along <strong>the</strong> Mariana island<br />
chain creating isolated areas of increased production. In addition, an anticyclonic eddy is <strong>for</strong>med off <strong>the</strong><br />
southwestern coast of Guam in <strong>the</strong> same region as <strong>the</strong> increased chl a (Wolanski et al 2003; Figure 2-6).<br />
It is likely that phytoplankton is becoming trapped within <strong>the</strong> eddy and is not advected to <strong>the</strong> west,<br />
allowing <strong>for</strong> an accumulation of biomass and chl a in <strong>the</strong> region. The remainder of <strong>the</strong> study area<br />
experiences chl a levels below 0.045 mg/m 3 throughout <strong>the</strong> year (NASA 1998; Figure 2-6). ENSO<br />
appears to have little, if any, effect on primary production in <strong>the</strong> western tropical Pacific (Mackey et al<br />
1997; Higgins and Mackey 2000).<br />
2.5.1.2 Chemosyn<strong>the</strong>sis<br />
Ano<strong>the</strong>r potentially significant source of biological productivity does not occur in <strong>the</strong> light of <strong>the</strong> surface,<br />
but ra<strong>the</strong>r at great depths within <strong>the</strong> ocean. In some locations, including <strong>the</strong> Mariana Trough,<br />
hydro<strong>the</strong>rmal springs can support vast benthic communities (Hessler and Lonsdale 1991; Hashimoto et<br />
al. 1995; Galkin 1997). Many organisms live in association with bacteria capable of deriving energy from<br />
hydrogen sulfide that is dissolved in <strong>the</strong> hydro<strong>the</strong>rmal vent water (Thurman 1997). Since <strong>the</strong>se bacteria<br />
are dependant upon <strong>the</strong> release of chemical energy, <strong>the</strong> mechanism responsible <strong>for</strong> this production is<br />
called chemosyn<strong>the</strong>sis. Little is known regarding <strong>the</strong> significance of bacterial productivity on <strong>the</strong> ocean<br />
floor on a global scale. Hydro<strong>the</strong>rmal indicators and vents have been found within <strong>the</strong> study area (Embley<br />
et al. 2004) and locations are described in fur<strong>the</strong>r detail in subsequent sections.<br />
2.5.2 Secondary Production<br />
Secondary production refers to <strong>the</strong> production (change in biomass) of organisms that consume primary<br />
producers, i.e., <strong>the</strong> production of bacteria and animals through heterotrophic processes (Scavia 1988;<br />
Strayer 1988). Detailed descriptions of protected species as consumers of primary production including<br />
marine mammals and sea turtles, as well as species such as corals and seagrasses are found in later<br />
sections of this chapter or later chapters of this MRA. In this section, marine zooplankton is discussed.<br />
<strong>Marine</strong> zooplankton are aquatic organisms ranging in size from 20 µm to large shrimp (>2,000 µm)<br />
(Parsons et al. 1984), and can be separated into two distinct categories based upon <strong>the</strong>ir dependence to<br />
coastal proximity. Oceanic zooplankton includes organisms such as salps and copepods typically found<br />
at a distance from <strong>the</strong> coast and over great depths in <strong>the</strong> open sea. Neritic zooplankton (found in waters<br />
overlying <strong>the</strong> island shelves), include such species as fish and benthic invertebrate larvae, and are<br />
usually only found short distances from <strong>the</strong> coast (Uchida 1983).<br />
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