2013
DOI: 10.1007/s00338-013-1066-5
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Direct and indirect effects of high pCO2 on algal grazing by coral reef herbivores from the Gulf of Aqaba (Red Sea)

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Cited by 19 publications
(13 citation statements)
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“…Broadbent et al ., ); (iii) dominated by shallow water autotrophs that routinely experience physiological stress likely to drive BVOC production (Baker et al ., ; Suggett & Smith, ) and (iv) exhibit complex ecological interactions that are known to be strongly mediated by biologically derived chemical products (e.g. DeBose et al ., ; Borell et al ., ).…”
Section: Introductionmentioning
confidence: 99%
“…Broadbent et al ., ); (iii) dominated by shallow water autotrophs that routinely experience physiological stress likely to drive BVOC production (Baker et al ., ; Suggett & Smith, ) and (iv) exhibit complex ecological interactions that are known to be strongly mediated by biologically derived chemical products (e.g. DeBose et al ., ; Borell et al ., ).…”
Section: Introductionmentioning
confidence: 99%
“…One consequence of naturally variable stress regimes is that some of the lessons being learnt through experimental manipulations of pCO 2 might actually have greater relevance for contemporary environments than previously thought. For example, high levels of pCO 2 have been found to induce elevated concentrations of the secondary metabolite dimethylsulfoniopropionate (DMSP) in the reef alga Ulva lactuca [84]. DMSP has many functions including herbivore defense, and the palatability of Ulva to a range of herbivores declined at higher concentrations of DMSP.…”
Section: New Perspectives and Research Opportunities On Coral Reefsmentioning
confidence: 99%
“…Loss of Acropora has a negative impact on corallivores [119] but could generate selection for omnivory. Macroalgae Corals (mediated by herbivores) If macroalgae increase their chemical defense from herbivores (secondary metabolite dimethylsulfoniopropionate) under highly elevated pCO 2 [84], they may also increase other defensive secondary metabolites (e.g., terpenes) that happen to have a negative allelopathic effect on corals [120]. Thus, corals would undergo selection to increase their tolerance to the chemical defenses of algae even though the primary driver of change in the algae could be escape from herbivory.…”
Section: Acroporid Coralsmentioning
confidence: 99%
“…Data from laboratory incubations with microalgae (760 latm; Avgoustidi et al 2012) and field mesocosm experiments with a mixed natural phytoplankton population (750 latm; Hopkins et al 2010) suggest a decrease in DMSP while several strains of the coccolithophore Emiliania huxleyi respond with an increase in intracellular DMSP under elevated pCO 2 (790 and 1000 latm) and a 4 to 6°C increase in temperature (Spielmeyer and Pohnert 2012;Arnold et al 2013). Similarly, varied is the response of DMSP to pCO 2 in seaweeds; Kerrison et al (2012) found no changes in DMSP in Ulva spp at 550-1250 latm, while Borell et al (2013) reported an increase in DMSP in Ulva lactuca following exposure to 4000 latm.…”
Section: Introductionmentioning
confidence: 99%