Global Seagrass Research Methods 2001
DOI: 10.1016/b978-044450891-1/50008-6
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Methods for the measurement of seagrass abundance and depth distribution

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Cited by 58 publications
(58 citation statements)
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“…The high annual precipitation in the tropical areas causes water clarity lower than that of northern and southern latitudes. Similar studies had been conducted in clear coastal waters and documented in [15,16], that were mostly in clear waters (Case-1) of Australia. Less efforts are required to obtain good STAGB results from the analysis of the images acquired during low spring tides, and as when seagrass leaves are exposed.…”
Section: Introductionmentioning
confidence: 78%
“…The high annual precipitation in the tropical areas causes water clarity lower than that of northern and southern latitudes. Similar studies had been conducted in clear coastal waters and documented in [15,16], that were mostly in clear waters (Case-1) of Australia. Less efforts are required to obtain good STAGB results from the analysis of the images acquired during low spring tides, and as when seagrass leaves are exposed.…”
Section: Introductionmentioning
confidence: 78%
“…The number of samples was determined after the elaboration of a performance curve for the macrofauna groups from a previous sampling. The subsequent samplings took into account the size of the small seagrass meadow studied here, as recommended by Duarte & Kirkman (2001), using a sampling design based on Burdick & Kendrick (2001) for patched meadows. Each core was sectioned in belowground and aboveground, the former of which included a thin upper layer (smaller than 0.5 cm) of the sediment.…”
Section: Methodsmentioning
confidence: 99%
“…One permanent 0.04 m 2 quadrat was established in the centre of each experimental plot at the commencement of the study. Stem density, percentage cover and maximum and average canopy heights (cm) were measured non-destructively in the permanent quadrats, as per Duarte & Kirkman (2001). Above-ground biomass was measured destructively in a 20 × 20 cm quadrat placed randomly in the sampling area of each plot.…”
Section: Methodsmentioning
confidence: 99%
“…All stems in the quadrat were cut off at sediment level and placed immediately in a bag. Later, the above-ground material was separated into leaf, stem and epiphyte components for every 10 cm layer of the canopy (as per Carruthers & Walker 1997) to determine leaf, stem and epiphyte biomass, and leaf and leaf cluster density, as per Duarte & Kirkman (2001). These components were counted and dried at 60°C for 48 h. To minimise destructive sampling of the plot area, a single core sample (0.01 m 2 , 20 cm deep) was collected from inside the above-ground biomass quadrat to quantify below-ground biomass.…”
Section: Methodsmentioning
confidence: 99%