Dataset: Sargassum mature growth conspecific - figure 4

[Reference cited below are from Dell et al (2016) Plos One.]
Study site and species:
This study was conducted between January and May in 2013 and 2015 on the coral coast of Fiji’s main island, Viti Levu, in the villages of Votua and Vatu-o-lailai (18°12’32S, 177°42’00E and 18°12’13S, 177°41’29E respectively; Fig 1). These villages are ~3km apart and each has jurisdiction over their stretch of reef flat; a habitat ranging between ~1.5 and 3m deep at high tide and between ~0 and 1.5m deep at low tide. In 2002, these villages established small areas (0.8km2 in Votua and 0.5 km2 in Vatu-o-lailai; Fig 1) as no-take MPAs [25]. Though MPA and non-MPA areas were initially similar in coral and macroalgal cover (33-42% macroalgal cover; 3-12% coral cover [25]), MPAs now differ significantly from the adjacent non-MPAs in benthic cover and fish diversity and abundance. MPAs now have ~56% live coral cover on hard substrate, ~2% macroalgal cover, ~8 fold higher biomass of herbivorous fishes, and higher recruitment of both fishes and corals than the non-MPAs [5,22]. Meanwhile the non-MPAs have lower fish biomass, 5-16% live coral cover on hard substrates and 51-92% macroalgal cover, the majority of which is comprised by Phaeophytes (primarily Sargassum polycystum C. Agardh [22]). In the MPAs, macroalgal cover is restricted to the shallowest, most shoreward areas (where access by herbivorous fishes appears limited), whereas macroalgal cover in the non-MPAs extends throughout the habitat. Thus, over distances of only a few hundred metres, there are dramatic differences in community composition that may impact the efficacy of factors controlling macroalgal populations, without the confounding factors of great differences in space or time.

Effect of conspecifics on survival and growth of mature fronds

To assess whether conspecific density might facilitate the survival and growth of mature fronds, we transplanted mature fronds into the centre of Sargassum beds and into nearby exposed habitats where they were isolated from others. Growth and duration of survival were measured over a two week period. Due to logistical constraints, this experiment was only conducted in Votua’s non-MPA where Sargassum beds were extensive and thus many separate patches were available for use.

Eight 10cm fronds of S. polycystum were removed from the centre of one holdfast, assuring genetic uniformity. Four were threaded through a three-strand rope (secured 5cm apart and 10cm from each end of the rope), and returned to the centre of the Sargassum bed (crowded condition) ~75m from shore at a depth of ~1m at low tide. The other four were threaded through a separate rope and tied in an area devoid of Sargassum two to four metres away (isolated condition). The ends of the rope were tied to the substrate to hold the rope in place. Twenty such rope pairs were set up with a total of 80 S. polycystum pieces in each of the crowded and isolated treatments. After two weeks the ropes were collected, the number of remaining fronds was counted and their length was measured. The initial length was subtracted from the final so that fronds that had been grazed in excess of growth were recorded as negative change.