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FUTURE RECORDING<br />
The species maps presented in this Atlas portray the<br />
broad patterns of Odonata distribution in Britain<br />
and, to a lesser extent, in Ireland. In the latter<br />
country, there is still much recording to be done<br />
before comprehensive maps can be produced,<br />
although the position has improved remarkably in<br />
the past decade. There is little doubt that basic<br />
recording will continue to fill in the distribution<br />
patterns of the commoner species in parts of Britain,<br />
and to identify some new sites for scarcer species<br />
(see also the section on Future distribution maps<br />
in the Fieldwork and data management chapter).<br />
The distribution of species is seldom static, and<br />
continued recording throughout the landscape will<br />
be needed to detect and monitor the changes which<br />
are taking place (Eversham 1994). Some species,<br />
such as Aeshna mixta, have attracted considerable<br />
attention in the context of possible climatic change<br />
(Watt, Ward & Eversham 1990). The example of A.<br />
mixta also stresses a recpirement of future recording<br />
which is already being addressed for other reasons:<br />
the need to establish proof of breeding. Highly<br />
mobile species such as A. mixta can occur as adults<br />
tens or hundreds of miles away from breeding sites.<br />
However, there is clear evidence that the present<br />
range expansion of A. mixta is an extension of<br />
breeding range, and not merely an increase in<br />
northward mobility (or even a higher level of<br />
detection of such mobility by recorders). It has<br />
been observed emerging from ponds in<br />
Derbyshire, Nottinghamshire and Yorkshire.<br />
Proof of breeding became a focus for recording in<br />
1988, with the launch of the Odonata Key Sites<br />
Project (KSP) (Merritt 1988). This is primarily an<br />
initiative in support of conservation. Although the<br />
broad patterns of distribution of each species were<br />
well known, as were the locations of many of the<br />
more important breeding sites for scarcer species,<br />
it was not possible to evaluate fully these sites<br />
relative to others owing to the lack of comprehensive<br />
breeding data. The new recording card, the RA70<br />
(Figure 12), provides space for information on each<br />
stage of the life cycle. The approach has already<br />
been used successfully at a county level, in the<br />
Cheshire dragonfly survey (Gabb & Kitching 1992).<br />
The authors have distinguished between proven,<br />
probable and possible breeding records. This<br />
distinction is of great importance, especially in<br />
relation to nature conservation, and it is hoped that<br />
county surveys in the future will follow their<br />
example.<br />
The RA70 also encourages recorders to estimate the<br />
abundance of each species. Even an approximate<br />
indication of numbers present is an improvement on<br />
122<br />
previous recording methods, and, taken over several<br />
years, KSP data are beginning to show which sites<br />
support significant populations of scarce species.<br />
No less valuable, it is becoming apparent which<br />
sites have unusually rich breeding assemblages<br />
(rather than merely having a long species list due to<br />
diligent observers noting species in transit). Given<br />
the continued support of recorders, the role of<br />
dragonflies in site assessment for nature<br />
conservation (Nature Conservancy Council 1989)<br />
can only increase.<br />
Two other areas of enhancement in recording also<br />
seem likely to play an important part in future: the<br />
recording of immigrant species and movement by<br />
resident Odonata, and the thorough monitoring of<br />
individual sites.<br />
Migrant butterflies such as the painted lady (Cynthia<br />
cardui) or the clouded yellow (Colias croceus) occur<br />
annually, and their occasional abundance attracts<br />
considerable attention. Similar movements among<br />
Odonata seem to be rarely detected. This may be<br />
because, unlike butterflies, the species of dragonfly<br />
most often involved are British/lrish resident<br />
species. The phenomenon is most obvious in the<br />
occasional arrival of species not normally present,<br />
such as Hemianax ephippiger or Sympetrum<br />
fonscolombii, records of which often find their way<br />
into the literature.<br />
Movement of resident species is much more difficult<br />
to evaluate, but any species which is able to<br />
colonise new habitats must pass through the<br />
unsuitable countryside in between: if resident<br />
species are observed in apparently unsuitable sites,<br />
or occur only for a few days and are not breeding,<br />
they are almost certainly wanderers. The appearance<br />
of S. danae away from heathland pools and<br />
acid peatlands may represent such long-distance<br />
movement. A scatter of recent records of Ischnura<br />
pumilio away from established breeding sites, and<br />
an observation of numerous post-emergent<br />
individuals flying almost vertically up-wards on<br />
warm days suggests the possibility that I. pumilio<br />
may be a 'wandering opportunist' (Fox 1989).<br />
Occasionally, dragonflies are seen flying in from the<br />
sea, sometimes in large numbers (Longfield 1948).<br />
Observers who spend all day in one place may see<br />
a steady stream of dragonflies pass them, flying<br />
along a river or over open countryside, perhaps all<br />
moving in the same direction. These may be rather<br />
rare events, but, if all observers are on the look-out,<br />
they may add up to a clearer picture of mobility<br />
within resident species. To this end, a recording<br />
form was drafted in 1991, and a revised version, the<br />
RA74 (Figure 13), was introduced in 1992.