We examined benthic microbial communities in 3 contrasting subtidal salt marsh sediments over the course of a year to investigate the relationship between environmental conditions and benthic microbial community structure. Samples were collected monthly from a high-energy sandy beach, a tidal creek bed, and a Spartina alterniflora marsh border. The concentrations and biomasses of benthic microalgae (BMA), total and potentially active bacteria (measured by an enzyme-activated fluorogenic compound), heterotrophic protists, and metazoan meiofauna were measured at each location. Sediment grain size and porewater pH explained most of the variability in biomass distributions; variations in benthic biomass did not correlate well with temperature. There was a seasonal shift from a BMA-dominated community in the spring and summer months to bacteria-dominated communities in autumn at all locations, when inactive bacteria were most abundant. When normalized to sediment porewater volume, benthic protists concentrations were not significantly related to sediment porosity. Benthic protist porewater concentrations (mean: 3.4 × 10 3 , range: 0.1 to 9.3 × 10 3 protists ml -1) were comparable to protist concentrations in the water column. In contrast, bacteria were several orders of magnitude more concentrated in the sediments (mean: 4.2 × 10 9 ; range: 0.6 to 16 × 10 9 bacteria ml -1 ) than the water column. Low abundances of protists relative to bacteria appear to contribute to long bacterial turnover times, especially in fine-grained sediments. We hypothesize that both grazing by meiofauna and low anaerobic growth efficiency lead to relatively low biomass of bacterivorous protists.
KEY WORDS: Marine sediments · Salt marsh · Microzoobenthos · Protists · Bacteria · Biomass
Resale or republication not permitted without written consent of the publisherMar Ecol Prog Ser 399: [15][16][17][18][19][20][21][22][23][24][25][26] 2010 derived carbon appeared in meiofauna within 1 h of the addition of 13 C bicarbonate; bacteria incorporated the labeled carbon within several hours (Middelburg et al. 2000). These and other observations suggest that algal-derived carbon is channeled through 2 discrete pathways: (1) directly to herbivorous metazoan meiofauna, or (2) through bacteria to the microbial food web (van Oevelen et al. 2006). However, exchanges between these trophic pathways also occur. For example, diatoms were ingested by both protists and meiofauna (Epstein 1997a) and ingestion of bacteria by meiofauna and microinvertebrates has been observed (Kemp 1987). Additionally, the linkages between bacterivorous microbenthos and meiofauna (Epstein & Gallagher 1992, Hamels et al. 2001a) indicate that the 2 major routes of carbon flow in benthic environments, at least at times, intersect.The processes regulating the abundance and activity of bacteria in sediments are especially important as sediment bacteria play a significant role in benthic metabolism and geochemistry by transforming carbon, nitrogen, and sulfur compounds (revi...