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2007
DOI: 10.1016/j.aquabot.2006.12.002
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Seasonal shifts in seagrass bed primary producers in a cold-temperate estuary: Dynamics of eelgrass Zostera marina and associated epiphytic algae

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Cited by 47 publications
(42 citation statements)
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“…Likewise, high abundances of G. fucicola have been related to detritus accumulation in seagrass meadows right after the decay of the leaves (Lepoint et al 2006). Furthermore, the increase in seagrass biomass favors the establishment of epiphytic algae, which bloom in August and provide additional food for secondary producers (Hasegawa et al 2007). This leads to high rates of the secondary production, with grazers such as amphipods of the families Dexaminidae and Amphitoidae as well as most of the isopods reaching their greatest abundances after late summer (Fredette et al 1990).…”
Section: Discussionmentioning
confidence: 97%
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“…Likewise, high abundances of G. fucicola have been related to detritus accumulation in seagrass meadows right after the decay of the leaves (Lepoint et al 2006). Furthermore, the increase in seagrass biomass favors the establishment of epiphytic algae, which bloom in August and provide additional food for secondary producers (Hasegawa et al 2007). This leads to high rates of the secondary production, with grazers such as amphipods of the families Dexaminidae and Amphitoidae as well as most of the isopods reaching their greatest abundances after late summer (Fredette et al 1990).…”
Section: Discussionmentioning
confidence: 97%
“…In particular, Zostera marina shows a clear seasonal dynamics, with elongation of the leaves and rhizomes in spring-summer and spreading of seeds in winter (Hasegawa et al 2007). This may be reflected in changes of the peracarid faunas, as indicated by the present study.…”
Section: Discussionmentioning
confidence: 98%
“…The assumption that productivity of kelp and seagrass in the Isles of Scilly is comparable to that of Norwegian kelp and Danish seagrass probably reduced the accuracy of estimates. Productivity of these plants is influenced by physical conditions such as temperature, water clarity, nutrient availability and competition with other flora and grazing fauna (Hasegaw et al, 2007), which may vary between the Isles of Scilly and the study sites where the productivity rates were determined. Exudate rates of seaweeds have been found to vary in the natural environment by up to 35% of the net assimilation value (Hatcher et al, 1977), which may have resulted in inaccuracies when the Norwegian kelp productivity data were transferred to the Isles of Scilly.…”
Section: Valuing Gas and Climate Regulationmentioning
confidence: 99%
“…There are many methods that have been used to determine benthic metabolism, including extrapolation from photosynthesis-irradiance curves (Kraemer and Alberte 1993), changes in primary producer biomass (Hasegawa et al 2007), mass balance models (Kemp et al 1997;Kaldy et al 2002), diel changes in water-column concentrations of either dissolved oxygen (DO) or dissolved inorganic carbon (''open-water'' method;D'Avanzo et al 1996;Ziegler and Benner 1998), and direct benthic flux measurements of DO or dissolved inorganic carbon in either in situ chambers or laboratory incubations of substrate cores (McGlathery et al 2001;Gazeau et al 2005;Yarbro and Carlson 2008). These conventional methods all have significant limitations.…”
mentioning
confidence: 99%