“…The sampling design was used to allow comparisons across different spatial scales, in which sampling points were spaced along three 1 km long transects repeating a sequences of inter-sample distances of 30 cm, 1, 5, 10, 30, 50, 100, 500 and 1000 m. The macrofauna cores were sieved on a 500 µm mesh sieve and macrofauna preserved in 70% isopropyl alcohol for later taxonomic identification (usually to species level). The percentage of seagrass Zostera mulleri, bare sand and shell hash cover was estimated through photographs (0.25 m 2 ) of each sampling point (Kraan et al 2015(Kraan et al , 2020a for detailed information). Mean sediment grain size and grain size fractions (silt < 63 μm, very fine 63-125 μm, fine 125-250 μm, medium 250-500 μm and coarse > 500 μm), as well as organic content (%), chlorophyll-a and phaeopigments (mg g −1 ) were estimated from a pool of three surface sediment cores (2 cm diam., 2 cm deep) at each sampling point.…”