2007
DOI: 10.1016/j.jembe.2007.06.017
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Impact of light limitation on seagrasses

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Cited by 397 publications
(320 citation statements)
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References 121 publications
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“…This confirms previous reports that H. ovalis can cope with short-term shading through physiological rather than morphological adaptation . Following the 21-day recovery, the persistence of larger leaves with lower sugar content in shaded than in unshaded plants is consistent with shading triggering a delayed 'light-harvesting' response through increased surface area, as observed in other seagrasses (Ralph et al 2007). The 60% higher initiation of apices with shading was probably a similar light stress response, which increased the potential for leaf production and harvesting of light, although this potential was not realised as there was no difference in the actual branching frequency (conversion of apices into new modules with leaves) between unshaded and shaded plants, and hence no difference in leaf density.…”
Section: Responses To Shadingsupporting
confidence: 75%
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“…This confirms previous reports that H. ovalis can cope with short-term shading through physiological rather than morphological adaptation . Following the 21-day recovery, the persistence of larger leaves with lower sugar content in shaded than in unshaded plants is consistent with shading triggering a delayed 'light-harvesting' response through increased surface area, as observed in other seagrasses (Ralph et al 2007). The 60% higher initiation of apices with shading was probably a similar light stress response, which increased the potential for leaf production and harvesting of light, although this potential was not realised as there was no difference in the actual branching frequency (conversion of apices into new modules with leaves) between unshaded and shaded plants, and hence no difference in leaf density.…”
Section: Responses To Shadingsupporting
confidence: 75%
“…. However, climax species have greater carbohydrate storages (due to thicker rhizomes) and can therefore withstand longer shading (Ralph et al 2007). In contrast, herbivory is a natural and intrinsic disturbance on seagrasses (for a review, see Valentine and Duffy 2006).…”
Section: Introductionmentioning
confidence: 99%
“…Macroalgae cover may reduce the C content of seagrasses for two reasons. First, light reduction by macroalgae mats may contribute to a decrease in photosynthetic activity of seagrasses (Brun et al, 2003;Huntington and Boyer, 2008;Peralta et al, 2002;Ralph et al, 2007). This can cause a subsequent reduction in root and rhizome growth of seagrasses (Hemminga, 1998), as rhizomes and roots are heterotrophic tissues depending on basipetal translocation of photosynthates and oxygen from active photosynthesizing leaves to persist (Zimmerman and Alberte, 1996).…”
Section: Fast Indicator Responses Of Seagrassesmentioning
confidence: 99%
“…Seagrass meadows have higher production relative to unvegetated sediments (Barró n et al 2004;Eyre et al 2011;Hume et al 2011) in part because they have greater primary producer and heterotrophic consumer biomass (Hemminga and Duarte 2000). In addition, changes in ecosystem structure through the development of a seagrass canopy can increase efficiency of light absorption on an ecosystem scale relative to unvegetated sites (Binzer et al 2006;Ralph et al 2007). Finally, seagrass communities affect flow conditions and create a depositional environment (Gacia and Duarte 2001;Hansen and Reidenbach 2012), increase sediment organic content (Fourqurean et al 2012;McGlathery et al 2012;Greiner et al 2013), and change sediment oxygenation through release of oxygen from the roots and rhizomes (Frederiksen and Glud 2006).…”
mentioning
confidence: 99%