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

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8.0 Eelgrass<br />

formation evident. While this bed appears persistent from previously reported observations,<br />

seasonal differences in eelgrass bed extent were apparent from the side-scan <strong>surveys</strong>.<br />

The Mitigation Site located in the center <strong>of</strong> the Pier 300/Seaplane Lagoon Area consisted <strong>of</strong><br />

large, evenly spaced plants with occasional dense patches that were less than 3 m 2 . Red algae<br />

(Chaetomorpha spp. <strong>and</strong> Gracillaria spp.) was commonly observed as potential competitors for<br />

space <strong>and</strong> light among the eelgrass plants <strong>and</strong> was particularly evident adjacent to the rock<br />

revetments <strong>and</strong> in areas with hard substrate (rock) or shell fragments. The southern portions <strong>of</strong><br />

the Pier 300 site contained higher densities <strong>of</strong> Gracillaria spp., to the extent that it was much<br />

more common than the eelgrass plants. Considering the Mitigation Site is composed <strong>of</strong> rock<br />

revetments constructed to support the dredge fill <strong>of</strong> various sizes, the occurrence on marine<br />

algae is not surprising based on the available substrate. Considering the location <strong>of</strong> the<br />

Mitigation Site between the small s<strong>and</strong>y beach embayment to the west, comprised <strong>of</strong> mostly fine<br />

s<strong>and</strong> <strong>and</strong> mud, <strong>and</strong> the deep dredged channel leading into the Seaplane Lagoon, circulation<br />

<strong>and</strong> scouring from tidal water movement likely contribute to the occurrence <strong>of</strong> courser sediments<br />

<strong>and</strong> the persistence <strong>of</strong> competitive algal species. Previous eelgrass transplantation that was<br />

conducted in 2003 <strong>and</strong> 2007 still appears spatially distinct <strong>and</strong> the associated eelgrass<br />

community is likely being shaped by the complex interactions <strong>of</strong> competition <strong>and</strong> hydrology that<br />

affects sediment distribution.<br />

The eelgrass bed within the Mitigation Site displayed very little season change, decreasing from<br />

15.4 acres in the spring to 15.1 acres in the fall (approximately 2.5%). The low density <strong>and</strong><br />

evenly spaced plants observed throughout this site coupled with dense aggregations <strong>of</strong><br />

Gracillaria spp. made evaluations <strong>of</strong> the differences in sonar <strong>surveys</strong> difficult. For example,<br />

although the imagery shown in Figures 8.3-4 <strong>and</strong> 8.3-5 depicts a continuous low density bed,<br />

the actual configuration <strong>of</strong> the site is likely more fragmented at a finer scale.<br />

The Terminal Site in the western most portion <strong>of</strong> the Pier 300/Seaplane Lagoon area is the most<br />

consistent eelgrass habitat within this portion <strong>of</strong> the Port <strong>and</strong> consists <strong>of</strong> uniform s<strong>and</strong>/mud<br />

substrate supporting a continuous, healthy bed <strong>of</strong> eelgrass with only intermittent occurrences <strong>of</strong><br />

algae (Chaetomorpha spp. <strong>and</strong> Gracillaria spp.). The Terminal Site extends from the s<strong>and</strong>y<br />

beach adjacent to the Mitigation Site to the south a<strong>long</strong> the riprap. The spatial extent <strong>of</strong> the<br />

Terminal Site bed decreased from 10.4 acres in the spring to 8.9 acres in the fall (approximately<br />

15%), with the bed contracting throughout the <strong>of</strong>fshore edge <strong>and</strong> the densest areas decreased<br />

overall (Figures 8.3-2 <strong>and</strong> 8.3-4). Seasonal differences in plant sizes were evident with the<br />

eelgrass bed a<strong>long</strong> the beach shifting from small <strong>and</strong> large plants in the spring to mostly large<br />

(>2 ft) plants in the fall, with a low epiphyte load. During both spring <strong>and</strong> fall <strong>surveys</strong> the<br />

eelgrass was evenly spaced, forming a continuous bed just inshore <strong>of</strong> a noticeable berm at<br />

approximately -5 to -8 ft MLLW. Extending south a<strong>long</strong> the riprap adjacent to the terminal, the<br />

substrate contained several dark areas <strong>of</strong> fine mud where the eelgrass bed became increasing<br />

discontinuous <strong>and</strong> sparse moving away from the beach <strong>and</strong> the riprap.<br />

In some cases considerable annual (seasonal) variation in abundance has been documented in<br />

southern California (e.g., winter die-<strong>of</strong>f <strong>and</strong> spring/summer re-growth) due to a variety <strong>of</strong> factors,<br />

including but not limited to physical <strong>and</strong> <strong>biological</strong> disturbance, changes in nutrient availability,<br />

<strong>and</strong> changes in water quality parameters such as turbidity <strong>and</strong> salinity. These factors can result<br />

in <strong>long</strong>-term changes in eelgrass abundance depending on the frequency <strong>and</strong> intensity <strong>of</strong><br />

unfavorable conditions. Eelgrass density also can vary substantially depending on the bottom<br />

depth <strong>of</strong> plant attachment. This is due to variations in the size <strong>of</strong> plant turions at different<br />

depths. For example, at shallower depths eelgrass density is typically greater than at deeper<br />

depths (Durance 2002 <strong>and</strong> Gussett 2002). Eelgrass density <strong>and</strong> morphology vary with respect<br />

to depth, exposure, substrate, <strong>and</strong> water clarity (Durance 2002). As a result, it can be difficult to<br />

define characteristics for a “normal” eelgrass bed.<br />

<strong>2008</strong> Biological Surveys <strong>of</strong> Los Angeles <strong>and</strong> Long Beach Harbors 8–13<br />

April 2010

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