London scoping - ukcip
London scoping - ukcip
London scoping - ukcip
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Final Report<br />
82<br />
of air pollution concentrations (Ashmore et al., 1985;) and water stress, with major reductions in<br />
the crown density of beech coinciding with droughts in southern Britain (Cannell and Sparks,<br />
1999). Natural woodlands suffering from drier summer conditions in the future may become<br />
more susceptible to insect pests, disease and windthrow during the stormier winter conditions.<br />
However, drought stress during summer can also afford protection from ozone damage by<br />
enforcing stomatal narrowing or closure (Zierl, 2002). Conversely, grass productivity is<br />
substantially reduced during hotter, drier summers (Sparks and Potts, 1999), pointing to<br />
increased water demand for lawn irrigation under the UKCIP02 scenarios.<br />
Bird populations are sensitive to many types of environmental change and, because they occupy<br />
a position at or near the top of the food-chain, give indications of overall ecosystem functioning.<br />
For example, the recent increase in grey heron numbers in <strong>London</strong> has been attributed to the<br />
improvement in water quality (leading to higher natural fish populations) and the absence of<br />
severe winters (Marchant et al., 1990). Small birds, like the wren, are particularly prone to<br />
prolonged spells of cold, wet or snowy weather, and therefore provide an excellent index of<br />
very cold winters. Records of the wren population on farmland and woodland since 1962 are<br />
strongly related to mean winter temperatures in central England, and have maintained relatively<br />
high numbers since the 1990s (Crick, 1999). Similarly, annual variations in the first laying<br />
dates are often strongly correlated with variations in spring temperatures (Crick et al., 1997), but<br />
mismatches in the timing of laying relative to food supplies can reduce bird populations (Visser,<br />
1998). Changes in migratory patterns and arrival dates have also been noted but this will<br />
depend on the specific trigger(s) for migration. For example, a 1ºC increase in spring<br />
temperature is associated with a 2-3 day earlier appearance of the swallow in the UK (Sparks<br />
and Loxton, 2001).<br />
Thus, climate change has the potential to affect future bird migration, winter survival, and egglaying.<br />
The MONARCH project assessed the impacts of six bioclimatic variables on the<br />
distribution of ten breeding birds at 10 x 10 km resolution under the UKCIP98 Low and High<br />
scenarios by the 2020s and 2050s (Berry et al., 2001). (Habitat, however, was not included in<br />
the training of the model and the ten birds studied are not all appropriate to <strong>London</strong>’s avifauna).<br />
Under the High scenario the most significant reductions in southeast England climate space<br />
occur for the willow tit, nuthatch and nightingale, due to warmer and drier conditions affecting<br />
woodlands and insects. Since woodland is the second most extensive natural habitat of <strong>London</strong>,<br />
these reductions could be reflected in the range of birds visiting the back gardens of suburban<br />
<strong>London</strong>. Conversely, the potential distribution of the reed warbler increases nationally, along<br />
with the yellow wagtail and turtle dove (which is contrary to the current decline in the latter<br />
two), probably reflecting an affinity for a warmer, drier climate. These results should, however,<br />
be treated with caution because the science underlying the MONARCH assumptions is less than<br />
complete.<br />
Insect distributions and the timing of insect activity are also highly weather dependent (Burt,<br />
2002). For example, the ranges of butterflies in North America and Europe have shifted<br />
poleward in response to rising temperatures (Parmesan, 1999). Extensive records of insects<br />
throughout Britain since the 1960s and 1970s indicate that a 1ºC increase in temperature is<br />
associated with a 16-day advancement in the first appearance of the peach-potato aphid, a 6-day<br />
advance in peak flight time of the orange tip butterfly, and an 8-day advancement in the time of<br />
activity of the common footman moth (Sparks and Woiwod, 1999). Finally, it is recognised that<br />
climate plays a dominant role in vector-borne diseases – directly through its effects on insect<br />
development, and indirectly through its effects on host plants and animals. Although it has been<br />
suggested that the most lethal form of malaria can not be transmitted by mosquitoes in the UK