Limitations in the use of PAM fluorometry for measuring photosynthetic rates of macroalgae at high irradiances
By S. Beer, L. Axelsson. 2004
107 citations recorded by the source corpus.
Subfields: Atmospheric Science, Oceanography
View Paper: https://www.semanticscholar.org/paper/24a25b5998b91388468b17e895bf59bf4d9d7e3f
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In Atmospheric Science
In Oceanography
Citations in the corpus
- Physiological responses of the calcifying rhodophyte, Corallina officinalis (L.), to future CO2 levels (2012, background): “In general, the rETR and O2 evolution data did not complement each other at high irradiances, which has been reported earlier to be a result of critically low yield values and photoinhibition at high irradiances (Hanelt and Nultsch 1995; Beer and Axelsson 2004).”
- The Use of the Fluorescence Signal in Studies of Seagrasses and Macroalgae (2010, background): “1998; Beer and Björk 2000; Franklin and Badger 2001; Beer and Axelsson 2004; Enríquez and Rodríguez-Román 2006; Nielsen and Nielsen 2008). In the former example taken from the experimental approach of Cayabyab and Enríquez (2007), apical and basal leaf sections, which differed in the absorption cros”
- Influence of salinity, temperature, dissolved inorganic carbon and nutrient concentration on the photosynthesis and growth of Fucus vesiculosus from the Baltic and Irish Seas (2008, background): “The reflection and absorption by non-photosynthetic pigments have earlier been found to be negligible while measuring under water (Beer et al , 2000 ; Beer & Axelsson, 2004 ).”
- Why is Ulva intestinalis the only macroalga inhabiting isolated rockpools along the Swedish Atlantic coast (2004, background): “For general explanations of the use of PAM fluorometry in marine macrophytes, see e.g. Beer et al. (2001), and for limitations of its use at high irradiances, see Beer & Axelsson (2003) and Carr & Björk (2003).”