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Notes: Abstract We followed changes in the neutral lipid content of actively swimming zoospores of the palm kelp Pterygophora californica in a laboratory experiment to investigate the degree to which spore swimming is fueled by endogenous lipid reserves. The neutral lipid content of individual zoospores during the experiment was measured by flow cytometry using Nile Red, a fluorescent stain that is specific for neutral lipid. Results showed that photosynthesis greatly influenced lipid consumption during zoospore swimming. We found no detectable change in the neutral lipid content of zoospores after 30 h of swimming under conditions where light was near the optimum for photosynthesis. By contrast, neutral lipid declined by ≃43% over 30 h in zoospores kept in the dark. To evaluate whether lipid reserves are generally related to spore motility in macroalgae, we surveyed spore lipid-content and composition in species with motile spores and non-motile spores using thin-layer chromatography (TLC), and flame-ionization detection (FID). We observed substantial differences in lipid content and composition among the 20 species examined. Spores high in total lipid (as estimated by the ratio of lipid:carbon) generally had a large amount of neutral lipid; motile spores had significantly more lipid and a significantly larger neutral lipid fraction than non-motile spores. The kelps as a group had the highest total lipid content and the largest neutral lipid fraction, while non-motile spores of red algae were generally low in total lipid and in the proportional abundance of neutral lipid. Phospholipids accounted for more than half of all lipid in 14 of the 20 species examined, while neutral lipid accounted for the majority of lipid in all five species of kelp examined. Triacylglycerols, which function primarily in energy storage, were the primary form of neutral lipid in all but one species of kelp (Agarum fimbriatum), whereas free fatty acids were the dominant form of neutral lipid in most red algae and in brown algae that had a small neutral lipid fraction. Our results are largely consistent with the hypothesis that macroalgae use endogenous lipid reserves to fuel spore-swimming. The small amounts of triacylglycerols observed in the motile spores of several species of brown and green algae, however, indicate that the amount of lipid reserves needed to fuel spore-swimming may be influenced by a variety of factors including swimming behavior, photosynthetic efficiency, and the light environment inhabited by spores.

Notes: Abstract Point sources of pollution (e.g. industrial and municipal outfalls) may produce ecological impacts at distant locations if pollutants affect dispersive propagules. We used laboratory experiments to determine how water-column exposure to produced water (=the aqueous fraction of oil and gas production that is typically discharged into coastal waters) influences the colonization potential of giant kelp (Macrocystis pyrifera) zoospores on the bottom. Zoospores were maintained in suspension at relatively low densities in 18-liter containers and exposed to one of five concentrations of produced water for varying amounts of time. Zoospore swimming generally decreased with increasing produced-water concentration and exposure duration; however, the specific pattern of decrease differed between experimental trials done on different dates. The effect of exposure duration on the ability of swimming zoospores to attach to plastic dishes placed on the bottom varied with produced-water concentration. Zoospores placed in produced-water concentrations of 1 and 10% showed a steady decline in their ability to attach with increased exposure; lower concentrations of produced water had no such effects. The percentage of zoospores that germinated after attachment varied tremendously with exposure duration and date of experimental trial. Zoospores that settled during the first 12 h after release had very poor rates of germination, indicative of a short precompetent period. Surprisingly, exposure of suspended zoospores to high concentrations of produced water during the first 12 h reduced this precompetent period and greatly improved germination success on the bottom. The magnitude of this enhancement, however, varied among dates. The results suggest that adverse effects of discharging produced water on planktonic zoospores of giant kelp would most likely be limited to the immediate vicinity of the outfall.

Notes: Abstract Field and laboratory experiments were used to investigate the spatial scale of benthic effects of an active nearshore produced-water (=aqueous wastes of oil and gas production) outfall on various components of recruitment in the giant kelp Macrocystis pyrifera. Results showed that discernible effects on all parameters measured were limited to areas very close to the outfall (〈50 m). Zoospore production in sporophytes transplanted to varying distances from the diffusers did not vary in a systematic way. Survival and successful reproduction (i.e., sporophyte production) of outplanted gametophytes varied significantly among experimental dates. Performance of these parameters was significantly reduced only at the site nearest the diffusers (5 m away). Poor gametophyte survival near the outfall may have resulted from exploitative competition with Beggiatoa sp. (a fast-growing filamentous marine bacteria that exploits areas high in hydrogen sulfide, an abundant constituent of the produced-water effluent) rather than from toxicity of produced water. Laboratory assays indicated that gametophyte reproduction and subsequent sporophyte production were inhibited at levels likely to occur within the near vicinity of the diffusers. Nonetheless, field data indicate that the lack of sporophyte production near the diffusers probably resulted from factors affecting gametophyte survival.

Notes: Abstract Spatial and temporal patterns of predation on seeds of the seagrass Phyllospadix torreyi S. Watson were quantified at four sites near Santa Barbara, California, USA. Over a period of four flowering seasons during 1995 to 1998, monthly patterns of seed fall and intensity of seed predation were similar among sites, but were temporally quite variable. Abundance of dispersed seeds varied greatly both among seasons and years. Within any one year, seeds were present in the environment every month, but they peaked in abundance during the fall months following the annual flowering period. Seeds were more abundant during the earlier years of the study. The intensity of predation steadily increased throughout the study period, from a low of ≤10% seeds consumed during 1995 to ∼50% consumption by 1997, and it was not correlated with abundance of seeds in the environment. Pre-dispersal seed loss also was estimated in two flowering seasons by counting the numbers of seeds consumed prior to release from the plant, and was relatively low (〈15%). No differences were detected among the four study sites in patterns of pre-dispersal loss. Field surveys were done at two sites to identify potential seed predators. Three of the most abundant species identified in these surveys were tested in the laboratory to determine size-specific patterns of feeding activity and to assess which early life stages of P. torreyi (fruits within spadices, dehisced fruits, seedlings) were most vulnerable to predation. All three of the early life stages were consumed. The crabs Pugettiaproducta (Randall) and Pachygrapsus crassipes Randall were much more voracious predators than the isopod Idotea resecata Stimpson.

Notes: Abstract Descriptive evidence that sandy surfaces and rock ledges inhibit progress of grazing sea urchins prompted an experimental investigation of physical obstacles to urchin movement in a subtidal area of reef and kelp off southern California in 1980. In laboratory experiments, we found that both red (Strongylocentrotus franciscanus) and purple (S. purpuratus) urchins can negotiate sand using their oral spines, although purple urchins are slower and more hesitant to do so. In field experiments, we observed the fates of starved red urchins transported to replicate plots within stands of sand-or rock-based understory kelp (Pterygophora californica). Urchins in rock plots retreated to nearby crevices from where they ate attached kelp. After finding kelp blades, urchins soon disappeared from sand plots because individuals in small groups may have difficulty holding and eating attached kelps on unconsolidated surfaces. In another experiment, red and purple urchins reached kelp on a rock ledge by mounting an artificial ramp. We conclude that by using their tube feet, individuals of both species move best over flat, hard surfaces, although soft substrate may constitute a major barrier only to purple urchins. In the absence of effective predator control, urchins can surmount most sand or rock barriers when water motion subsides. Hence, their ability to coordinate spine movements to negotiate soft substrates may be an adaptation to invade kelp refuges during quiet periods if preferred drift food is unavailable.