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Climate Change and the European Water Dimension - Agri ...

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Aulacoseira spp. favour <strong>the</strong> changed conditions during spring overturn (Lund 1966,<br />

Round et al. 1990). These diatom blooms can collapse for a variety of reasons, but<br />

<strong>the</strong>rmal stratification <strong>and</strong> sedimentation usually accelerates <strong>the</strong>ir rate of decline.<br />

Once <strong>the</strong> diatoms have departed, a variety of small flagellates <strong>the</strong>n tend to dominate<br />

<strong>the</strong> plankton. These small forms have high rates of growth but can only survive if <strong>the</strong><br />

water column is periodically mixed by <strong>the</strong> wind.<br />

In lakes which do not freeze in winter, <strong>the</strong> timing of <strong>the</strong> spring bloom is mainly<br />

dependent on light <strong>and</strong> turbulence, two factors influenced by climatic variation <strong>and</strong><br />

change. Lund (1950) <strong>and</strong> Talling (1971) detailed <strong>the</strong> influence of stratification <strong>and</strong><br />

spring rains on <strong>the</strong> timing <strong>and</strong> magnitude of spring diatom blooms. A critical factor is<br />

<strong>the</strong> time <strong>the</strong> growing cells spend in <strong>the</strong> illuminated <strong>and</strong> dark portion of a mixed water<br />

column. Phytoplankton suspended in ‘dark’ water cannot grow because <strong>the</strong>ir<br />

respiratory losses are greater than <strong>the</strong>ir gross rate of carbon fixation.<br />

Catchement processes<br />

(Vegetation, Soil etc.)<br />

Nutrients<br />

Temperature<br />

The magnitude of <strong>the</strong> bloom may be differently related to climatic factors. The loss<br />

of ice cover or less snow on <strong>the</strong> ice might change <strong>and</strong>/or increase <strong>the</strong> algae<br />

population during winter (Pettersson, 1990; Adrian et al., 1995). Thus, <strong>the</strong> nutrient<br />

availability might be lower for <strong>the</strong> actual spring bloom, leading to a reduced algae<br />

peak (Pettersson 1990). Cloud conditions in spring, <strong>the</strong> mixing regime, <strong>and</strong> <strong>the</strong> timing<br />

of <strong>the</strong> onset of stratification strongly affect <strong>the</strong> magnitude of <strong>the</strong> phytoplankton spring<br />

peak (Gaedke et al., 1998a,b) <strong>and</strong> <strong>the</strong> annual primary production alpine lakes<br />

(Goldman et al., 1989). In extreme mild winters in Europe (i.e. 1989 <strong>and</strong> 1990) an<br />

coherent increase in cyanobacterial biomass was found in a number of <strong>European</strong><br />

lakes (Weyhenmeyer et al., 2002).<br />

Overwintering<br />

Relatively small differences in <strong>the</strong> overwintering stocks of some algae can have a<br />

major effect on <strong>the</strong>ir growth rate later in <strong>the</strong> year. For many slow-growing species of<br />

phytoplankton, <strong>the</strong>ir growth rate in early summer is strongly influence by <strong>the</strong> number<br />

of cells that overwinter in <strong>the</strong> open water (Heaney <strong>and</strong> Canter, 1989). Wet winters<br />

invariably reduce <strong>the</strong> size of this spring inoculum, which may <strong>the</strong>n influence <strong>the</strong><br />

seasonal succession of phytoplankton later in <strong>the</strong> year. Also <strong>the</strong> overwintering<br />

success of resting stages, for example of Gloeotrichia echinulata, a dominant<br />

75<br />

Mixing<br />

Processes<br />

Figure IV.B.5. Conceptual diagram of climate impacts on catchment <strong>and</strong> lake<br />

processes, <strong>and</strong> <strong>the</strong>ir relations (Modified by Dokulil from Anderson, 2000)<br />

Lake Biota

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