Photosynthetic responses of seven tropical seagrasses to elevated seawater temperature

By S. Campbell, L. McKenzie, Simon P. Kerville. 2006

198 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/18c6eb1edfd5cea277cc58c7f6f7e1a5f20a9107

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Citations in the corpus

Tropical seagrass meadows modify seawater carbon chemistry: implications for coral reefs impacted by ocean acidification (2012, background): “Direct effects include species differences in production [59] and their sensitivity to environmental stressors [40, 60] while indirect effects include differences in the faunal assemblages that seagrass communities support [61].”
Effects of irradiance, temperature, and nutrients on growth dynamics of seagrasses: A review (2007, methodology): “Pulse amplitude modulated (PAM) fluorometers have been used to measure the effects of thermal stress on chlorophyll a fluorescence (Ralph, 1998; Seddon and Cheshire, 2001; Campbell et al., 2006).”
Climate change and Australian marine life (2007, background): “Physiology Extreme temperatures, both warm and cool, if severe or prolonged can lead to irreparable damage and death of coastal organisms as well as photosynthetic inhibition in marine plants (Bruhn & Gerard 1996, Ralph 1998, Davenport & Davenport 2005, Campbell et al. 2006).”
Long-term climate-associated dynamics of a tropical seagrass meadow: implications for the future (2011, background): “Seagrasses are widely known to be sensitive to elevated temperature, with both laboratory and field data indicating that tropical seagrasses undergo thermally induced physiological stress at temperatures >35°C (Bulthuis 1983, Ralph 1998, Campbell et al. 2006).”
Thermal tolerance of two seagrass species at contrasting light levels: Implications for future distribution in the Great Barrier Reef (2011, background): “The optimum temperatures for photosynthesis and for maximizing P : R ratios are also not known for many—particularly tropical—seagrass species (Bulthius 1987; Campbell et al. 2006; Rasheed and Unsworth 2011).”
Climate change and ocean acidification effects on seagrasses and marine macroalgae (2013, background): “…established in longer term seasonal exposures are slightly lower than limits established in short-term pulsed experiments simulating midday or intertidal high temperature conditions (McMillan, 1984; Erftemeijer & Herman, 1994; Seddon & Cheshire, 2001; Campbell et al., 2006; Collier et al., 2011).”
Climate Change Impacts on Seagrass Meadows and Macroalgal Forests: An Integrative Perspective on Acclimation and Adaptation Potential (2018, background): “Due to the characteristics of any enzymatic reaction, also this enzymatic dissipation mechanisms can be impaired outside the thermal optimum of each species (Campbell et al., 2006; Repolho et al., 2017).”
The Use of the Fluorescence Signal in Studies of Seagrasses and Macroalgae (2010, background): “1999; Seddon and Cheshire 2000); (5) water flow (Enríquez and Rodríguez-Román 2006); (6) temperature (e.g., van de Poll et al. 2002; Campbell et al. 2006); (7) osmotic stress (e.”
Effects of a simulated heat wave on photophysiology and gene expression of high- and low-latitude populations of Zostera marina (2011, methodology): “In seagrasses, pulse amplitude modulated (PAM) fluorometry has been commonly used for studying the effects of environmental stressors on a suite of photophysiological parameters (Ralph et al. 1998, Campbell et al. 2006, Sharon et al. 2009).”
Impact of light limitation on seagrasses (2007, background): “For species pushed to even higher temperatures (up to 35 °C) increased photorespiration and photoinhibition may occur (Bulthuis, 1987; Campbell et al., 2006 ).”