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Sexual productivity and spring intramarsh distribution of a key salt-marsh microbial secondary producer
Authors:Steven Y Newell  Jennifer Wasowski
Institution:1. Marine Institute, University of Georgia, 31327, Sapelo Island, Georgia
Abstract:Phaeosphaeria spartinicola is known to be an important fungal (ascomycetous) secondary producer in the smooth-cordgrass (Spartina alterniflora) decomposition system of western Atlantic salt marshes, yet its degree of predominance among the ascomycete assemblages of salt marshes and the concentration of its sexual reproductive structures (ascomata) have been largely unknown. During May–June, we measured by direct microscopy the percent occupancy of leaf abaxial area and concentrations of ascomata in leaf blades of smooth cordgrass at three elevations in three drainage systems within the marshes of Sapelo Island, Georgia, United States. We also measured in water-saturation chambers the rates at which the ascomata expelled ascopoores (sexual propagules) out of decaying leaves from marsh sites containing or not containing shredder gastropods.P. spartinicola ascomata were found at averages of 36% to 93% of grid-circles (3-mm radius) on decaying leaf blades, with lower values at points directly adjacent to the leaf sheath, on leaves at earlier stages of decay, and at elevational subsites where shredder snails were more active. Marsh elevation had no effect of its own on percent occupation. No other species of ascomycetes were found at overall avarage frequencies greater than 3%. Average concentration of ascomata along the intervascular rows where they were located was 1 ascoma per 0.5 mm row (~1000 cm?2 abaxial leaf surface, translating to production of 1.6×107 ascomata m?2 intermediate-height marsh per standing crop of living stems). The fraction of total fungal production allocated to ascomata is speculatively and crudely estimated at about 9%, without taking into account potential loss to invertebrate shredders. At sites with abundances of snails >-50 m?2 peaks of ascospore expulsion (about 50–75 spores cm?2 leaf h?1, 3–5× the overall average rate) observed at snail-free sites were absent. Our measured rate of ascospore expulsion (averaged over snail-free and high-snail sites, and possibly an underestimate) translated to 6.5×104 spores m?2 marsh h?1 for times of freshwater saturation of leaves, and one-third that value for times of saltwater wetting.
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