Climate Change and the European Water Dimension - Agri ...
Climate Change and the European Water Dimension - Agri ...
Climate Change and the European Water Dimension - Agri ...
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eastern <strong>and</strong> western side of <strong>the</strong> North Atlantic indicate that <strong>the</strong> response of <strong>the</strong><br />
biosphere to climate change may exhibit complex behaviour. This kind of response is<br />
mediated through complex regional interactions with existing hydro-climatic channels<br />
such as <strong>the</strong> NAO. Indeed, <strong>the</strong> inverse response of ecosystems to climatic features on<br />
<strong>the</strong> two sides of <strong>the</strong> North Atlantic Ocean is consistent with <strong>the</strong> spatially<br />
heterogeneous nature of <strong>the</strong> climatic manifestations induced by this dominant mode<br />
of atmospheric variability (Dickson et al. 1996; Drinkwater 1996).<br />
These large-scale biogeographical changes have deeply impacted <strong>the</strong> diversity of<br />
calanoid copepods in <strong>the</strong> North Sea (Beaugr<strong>and</strong> 2003; 2004). Calanoid copepod<br />
diversity has increased in that region due to an increase in warm-water species<br />
(Figure IV.C.11). These modifications seem to be a response of pelagic ecosystems<br />
to an augmentation in sea surface temperature positively correlated to Nor<strong>the</strong>rn<br />
Hemisphere Temperature anomalies <strong>and</strong> may have a strong impact for <strong>the</strong><br />
functioning of <strong>the</strong> ecosystems, biogeochemical cycles <strong>and</strong> exploited resources<br />
(Figure IV.C.12). Using a plankton index indicator of <strong>the</strong> quality <strong>and</strong> quantity of prey<br />
available for larval cod survival in <strong>the</strong> North Sea, Beaugr<strong>and</strong> et al. (2003) showed<br />
that long-term changes in <strong>the</strong> index paralleled changes in cod recruitment at age 1<br />
<strong>and</strong> <strong>the</strong>refore larval cod survival (Figure IV.C.12). The index revealed a clear<br />
distinction between <strong>the</strong> periods 1963-1983 <strong>and</strong> both <strong>the</strong> periods 1984-1999 <strong>and</strong><br />
1958-1962 (Figure IV.C.12). The period 1963-1983 (‘Gadoid Outburst’, Cushing<br />
1984) was characterized by high abundance of prey for larval cod (positive<br />
anomalies in <strong>the</strong> biomass of calanoid copepods, in <strong>the</strong> abundance of C.<br />
finmarchicus, euphausiids <strong>and</strong> Pseudocalanus spp.) <strong>and</strong> a high mean size of<br />
calanoid copepods. Larval cod survival decreased from <strong>the</strong> mid-1980s, coincident<br />
with unfavourable changes in <strong>the</strong> plankton ecosystem, compared to <strong>the</strong> earlier period<br />
1963-1983. The change in <strong>the</strong> quality <strong>and</strong> quantity of plankton prey was related<br />
negatively to fluctuations in sea surface temperature. Increasing sea temperature<br />
may have had a double negative impact on larval cod survival in <strong>the</strong> North Sea.<br />
Figure IV.C.12. The regime shift in <strong>the</strong><br />
North Sea. Long-term changes in fish<br />
abundance in relation to year-to-year<br />
changes in calanoid copepod<br />
composition <strong>and</strong> hydrometeorological<br />
forcing. a. Long-term<br />
changes in gadoid recruitment<br />
(especially cod). b. Long-term changes in<br />
calanoid copepod species composition<br />
(in red: warm-water copepod calanoid<br />
species; in blue: cold-water calanoid<br />
copepod species). c. <strong>Change</strong>s in<br />
hydrological variables (sea surface<br />
temperature). d. <strong>Change</strong>s in large-scale<br />
hydro-climatic forcing (Nor<strong>the</strong>rn<br />
Hemisphere Temperature anomalies).<br />
From Beaugr<strong>and</strong> (2004).<br />
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