Nitrogen fixation was associated with the rinsed roots and rhizomes of the seagrass, Zostera marina L. Nitrogenase activity (acetylene reduction) was greater on rhizomes compared to roots, and on older roots and rhizomes relative to younger tissue. Compared to aerobic assays, anaerobic or microaerobic conditions enhanced the rate of acetylene reduction by rhizomes with attached roots, with the highest activity (100 nanomoles per gram dry weight per hour) occurring at PO2 = 0.01 atmosphere. Addition of glucose, sucrose, or succinate also increased the rate of acetylene reduction under anaerobic conditions, with glucose providing the most stimulation. In one experiment, comparison of acetylene reduction assays with '5N2 incorporation yielded a ratio of about 2.6:1. Seagrass communities are thought to be limited by the availability of nitrogen and, therefore, nitrogenase activity directly associated with their roots and rhizomes suggests the possibility of a Nrfixing flora which may subsidize their nutritional demand for nitrogen.In seagrass communities, as in many marine ecosystems, nitrogen in a combined form is often present at limiting levels (12, 13). Nonetheless, these communities are very prolific (11). Nitrogen fixation has been detected in rhizosphere sediments of several seagrasses (4, 6). The presence of a root-associated N2-fixing flora would assist in reconciling the observed productivities of these marine angiosperms with apparent nutrient impoverishment.The objectives of this study were 3-fold: (a) to locate within the rhizosphere the predominant sites ofnitrogen fixation; (b) with bay water to the laboratory. The time span between sampling and laboratory work was about 1 to 2 h. Upon return to the laboratory, emergent leafmaterial was removed from the sediment surface. The remaining roots, rhizomes, and sediment were placed into flasks containing nucleopore (0.2 pm) filtered Bellport bay water. These procedures were carried out while gassing with O2 free N2. The bubbling action effectively rinsed the roots and rhizomes of sediment and minimized exposure to O2 during assay set up. Approximately five 2-to 3-cm segments of roots and/or rhizomes were transferred into each of at least twelve 125-ml Erlenmeyer flasks containing 25 ml of filtered bay water. The flasks were sealed with rubber stoppers following an additional 2 min ofbubbling with N2 and then were evacuated and backflushed with N2 four to five times to ensure anaerobic conditions. Acetylene Reducdon Assays. The acetylene reduction technique (7), as adapted for use in seagrass systems (4, 6), was employed to measure nitrogenase activity. The flasks were placed into a 25°C shaking (100 rpm, rotary) water bath followed by the addition of 12.5 ml acetylene (pC2H2 = 0.12 atm). Preliminary experiments indicated saturation by 0.10 atm pC2H2. Ethylene and acetylene concentration were measured by flame ionization gas chromatography (4, 6).In all assays, triplicate flasks were incubated at each level of an experiment. In one experiment, rhiz...
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