Cyanobacterial dominance in lakes
By M. Dokulil, Katrin Teubner. Hydrobiologia, 2000
716 citations recorded by the source corpus.
Subfields: Ecology, Environmental Chemistry, Oceanography
View Paper: https://www.semanticscholar.org/paper/a275ed1e4240799d9af78fab659cb18d7e3ac0bf
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In Ecology
- G. Davies
- C. Gobler
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In Environmental Chemistry
In Oceanography
Citations in the corpus
- Morphological and physiological changes in Microcystis aeruginosa as a result of interactions with heterotrophic bacteria (2011, background): “The formation of colonies and aggregates is of decisive importance for the physiology and behaviour of cyanobacteria (Dokulil & Teubner, 2000).”
- Phytoplankton community in the tropical lake of Lagoa Santa (Brazil): Conditions favoring a persistent bloom of Cylindrospermopsis raciborskii (2009, background): “Lagoa Santa presented relatively high total-N:total-P ratios throughout the year, being always higher than the critical value of 29 suggested to favor the dominance of cyanobacteria (Smith 1983) or the value of 16 suggested to favor N2-fixing cyanobacteria (Dokulil and Teubner 2000).”
- The role of nitrogen in promoting the toxic cyanophyte Cylindrospermopsis raciborskii in a subtropical water reservoir (2006, background): “Therefore the nitrogen-fixing capacity that has often been suggested as one of the reasons why C. raciborskii dominates in lakes and reservoirs is unlikely to be an explanation in North Pine reservoir (Harris & Baxter, 1996; Padisák, 1997; Dokulil & Teubner, 2000; McGregor & Fabbro, 2000).”
- Abundance and toxicity of Planktothrix rubescens in the pre-alpine Lake Ammersee, Germany (2009, background): “Metalimnic oxygen values regularly were minimal at the end of September and in October, i.e. 3.7 mg I-I in 1999,4.0 mg 1- 1 in 2001, 5.1 mg I-I in 2002. and 4.6 mg 1-' in 2003.”
- Trophic interactions and consequent impacts of the invasive fish Pseudorasbora parva in a native aquatic foodweb: a field investigation in the UK (2010, background): “may reflect dominance by cyanobacteria of the phytoplankton community ( Dokulil and Teubner 2000 ).”
- Morphological Response of Microcystis aeruginosa to Grazing by Different Sorts of Zooplankton (2006, background): “Microcystis aeruginosa Kütz, a bloom-producing cyanobacterium found in both fresh and marine waters (Reynolds & Walsby, 1975; Dokulil & Teubner, 2000; Tsujimura et al., 2000; Landsberg, 2002; Lehman et al., 2005), which occurs as large colonial morph under natural conditions, exists mainly as…”
- Deciphering the effects of nitrogen, phosphorus, and temperature on cyanobacterial bloom intensification, diversity, and toxicity in western Lake Erie (2019, background): “Microcystis is more likely to benefit in deeper, stable water conditions, such as Maumee Bay, due to its ability to regulate its bouyancy (Dokulil and Teubner 2000), allowing it to remain within surface waters to prevent against light limitation as well as migrate to deeper nutrient-rich waters.”
- Same same but different: ecological niche partitioning of planktonic freshwater prokaryotes (2013, background): “They can form dense blooms, with some taxa being able to regulate their buoyancy by gas vacuoles or to produce toxins as grazing defense agents (Dokulil and Teubner, 2000; Posch et al., 2012).”
- The ecology of the invasive cyanobacterium Cylindrospermopsis raciborskii (Nostocales, Cyanophyta) in two hypereutrophic lakes dominated by Planktothrix agardhii (Oscillatoriales, Cyanophyta) (2010, background): “agardhii can grow well at much lower temperatures, 6–16°C (Berger, 1989 ; Dokulil & Teubner, 2000 ) and long-lasting populations have been observed in highly eutrophic reservoirs even during winter (Berger, 1975 ; Post et al.”
- RECRUITMENT OF BENTHIC MICROCYSTIS (CYANOPHYCEAE) TO THE WATER COLUMN: INTERNAL BUOYANCY CHANGES OR RESUSPENSION? 1 (2004, background): “There are several possible reasons for the success of Microcystis (Hyenstrand et al. 1998, Dokulil and Teubner 2000).”