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appendix b final 2008 biological surveys of los angeles and long ...

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8.0 Eelgrass<br />

<strong>surveys</strong>. No eelgrass beds were identified within the Port <strong>of</strong> Long Beach. One area just outside<br />

the Port’s boundary line northeast <strong>of</strong> Isl<strong>and</strong> Grissom was identified as supporting a sizeable<br />

eelgrass bed.<br />

Additional sparse eelgrass beds have been reported within Cabrillo Marina <strong>and</strong> intermittently in<br />

small narrow linear b<strong>and</strong>s a<strong>long</strong> riprap where suitable depth <strong>and</strong> conditions exist (Merkel &<br />

Assoc. 2009, pers. comm.). Eelgrass is <strong>of</strong>ten displaced by natural <strong>and</strong> anthropogenic events<br />

(e.g., storms <strong>and</strong> boat anchoring, respectively) eventually resettling in new areas that may<br />

provide suitable conditions for growth within limited time periods. However, the development<br />

<strong>and</strong> persistence <strong>of</strong> such outlying patches is ultimately tied to the stability <strong>of</strong> the substrate <strong>and</strong><br />

sufficient, consistent clarity <strong>of</strong> the overlying water column.<br />

8.3.3 Eelgrass Characteristics<br />

Leaf blade morphology characteristics <strong>and</strong> widths were documented for several locations during<br />

the fall <strong>surveys</strong> to determine whether more than one species <strong>of</strong> eelgrass was present within the<br />

surveyed beds. Leaf blades collected from the Cabrillo North eelgrass bed (n = 15) were<br />

measured for width. All measured blades were described as flat in cross section consistent with<br />

Zostera marina (as described in Coyer et al. 2007) <strong>and</strong> overall eelgrass blades had a low<br />

epiphytic load consisting <strong>of</strong> primarily diatom film <strong>and</strong> crustose coralline algae.<br />

Recent publications (Coyer et al. 2007, Engle <strong>and</strong> Miller 2003) confirmed that up to three<br />

species <strong>of</strong> eelgrass (Zostera spp.) may inhabit various areas <strong>of</strong> southern California, although<br />

their optimal growth requirements <strong>and</strong> transport mechanisms are not completely understood.<br />

During the fall diver verification <strong>surveys</strong>, eelgrass widths <strong>and</strong> morphology were recorded <strong>and</strong><br />

described by a visiting researcher (Dan Martin, University <strong>of</strong> South Alabama) <strong>and</strong> he identified<br />

two distinct blade cross sections. Collections were taken from Cabrillo North, Seaplane Lagoon,<br />

<strong>and</strong> the Mitigation Site. Cabrillo North samples averaged 4.1 mm (n=15) in width <strong>and</strong> all<br />

displayed a flat blade. In contrast, approximately 30% <strong>of</strong> all collected samples (n = 25) from the<br />

Seaplane Lagoon <strong>and</strong> the Mitigation Site had a W-shaped cross section <strong>and</strong> several displayed a<br />

prominent mid rib. The differences in eelgrass blade morphology suggest that more than one<br />

species <strong>of</strong> Zostera spp. may exist in the Ports <strong>and</strong>/or that some degree <strong>of</strong> hybridization may<br />

have taken place within eelgrass areas surveyed. More in-depth morphological investigations<br />

would be required to fully describe the variations among individual plants <strong>and</strong> eelgrass beds, but<br />

current findings indicate that eelgrass recruitment or transplantation events may have multiple<br />

sources.<br />

8.3.4 Comparison <strong>of</strong> 2000 <strong>and</strong> <strong>2008</strong> Surveys<br />

In general, <strong>2008</strong> delineated eelgrass beds were similar in area <strong>and</strong> location to those surveyed<br />

during the 2000 baseline survey (Figure 8.3.6). Turion densities from diver transects indicated<br />

that Cabrillo North <strong>and</strong> South supported the greatest densities <strong>and</strong> least variable eelgrass areas<br />

while the Pier 300/Seaplane Lagoon Area was variable <strong>and</strong> patchy in nature (Table 8.3-5, 8.3-6,<br />

<strong>and</strong> 8.3-7). The greatest turion densities within quadrats from the <strong>2008</strong> <strong>surveys</strong> were<br />

comparable to densities from the 2000 baseline study using slightly different quadrat placement<br />

methods (Table 8.3-9).<br />

In the previous baseline study (MEC 2002) turion density was estimated by selectively counting<br />

turions within the densest st<strong>and</strong>s <strong>of</strong> eelgrass for each identified eelgrass community. While<br />

those reported densities provided valuable information on the densest areas <strong>of</strong> eelgrass within<br />

specific beds they were not representative <strong>of</strong> the entire area or the majority <strong>of</strong> the surveyed<br />

eelgrass communities. In contrast, the eelgrass communities were elevated as follows. Density<br />

counts were organized by selecting the most prominent eelgrass beds observed from side-scan<br />

8–10 <strong>2008</strong> Biological Surveys <strong>of</strong> Los Angeles <strong>and</strong> Long Beach Harbors<br />

April 2010

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