CES in Europe
CES Methods
Each year CES ringers are asked to make a standard number of visits
to their site spread evenly between early May and late August. The
same set of mist nets is erected in the same positions on each of
the main visits. The total length of standard netting is decided
by the ringer, but is typically 100-200m. Ringers are asked to operate
their set of standard nets for at least six hours on each visit
and to standardise their chosen duration. A typical regime (in Britain)
would be to begin netting at dawn and continue until 1100hrs on
each of twelve visits. The scheme has some flexibility and permits
additional nets to be used during main visits, and also extra visits.
Most constant effort sites are located in either wet or dry scrub,
reedbeds or deciduous woodland. Sites in coniferous woodland are
not accepted because rapid tree growth is likely to cause short-term
changes in catching efficiency and the local bird community. Potential
constant effort sites are proposed by volunteer ringers, and are
generally accepted into the scheme as long as they are located in
suitable habitats and are not considered to be undergoing major
successional changes. The aim is to have a number of sites with
a good geographical spread across the country, so that national
figures may be usefully generated. In most schemes there is some
level of habitat recording, so that some idea of the representativeness
of sites can be formed, and successional (and other) changes in
vegetation structure and composition can be quantified.
Data collection and routine analysis
A certain minimum amount of information should be collected and,
ideally, this should be submitted in electronic form by the ringers,
or computerised later. The basic information to be collected for
each bird includes: ring number, species, age, sex (where appropriate)
and date(s) of capture. Additional information on biometrics, moult
and breeding status (for example extent of brood patch in females)
can usefully be collected and broadens the scope of possible analyses.
In Britain and Ireland, the availability of software for submitting
ringing data (IPMR, developed by a volunteer ringer) means that
the majority (>95%) of CES capture data are submitted electronically
via email or computer disc. The small number of paper submissions
are computerised and checked by BTO staff.
Using changes in standardized catch sizes we are able to measure
long-term changes in the abundance of adult and juvenile birds.
Long-term changes in catches of songbirds are of much greater conservation
interest than annual fluctuations, which may be linked to particular
weather events, for example. The indices of abundance and productivity
generated by CES ringing have been compared to those other schemes,
especially in Britain where many years data are available, to assess
their validity.
For most species long-term changes in the number of adult birds
caught on CES sites are very similar to changes in the numbers of
territories counted on Common Birds Census (CBC) plots, suggesting
that such standardised mist-netting is a reliable method for assessing
extensive changes in songbird populations (Crick et al.
2004). Similarly, the percentage of juveniles in the catch is a
good indicator of overall breeding success. Several intensive studies
have shown that annual catches of young birds in CES mist-nets do
accurately reflect local breeding success (e.g. du Feu & McMeeking
1991).
Many passerines show strong site fidelity to breeding sites in
successive breeding seasons, so regular sampling of breeding birds
can be an effective means of generating between-year recaptures
which can be used to estimate survival (return) rates of adult birds.
Although most of the well established schemes have a good number
of sites participating, mark-recapture data from individual sites
are often quite sparse and survival estimates for single sites often
lack precision (Peach 1993). This combination of a large numbers
of sites, each contributing relatively few individuals, provides
large technical challenges for estimating survival rates. Recent
advances in analytical techniques, however, allow mark-recapture
data to be pooled across CE sites, which can lead to considerable
improvements in precision. Work is now in progress to develop routine
production of survival rate indices from the British CES scheme.
Map of CES Schemes in Europe. Countries in dark
green are the three longest-running schemes.

Summary of CES Schemes in Europe operating
at June 2004. Details are given on the average number of
sites operating in each year, the number of visits made and nets
used at each site, together with an indication of whether they operate
over the whole breeding season.
| |
Year
started |
Number
of sites |
Number
of visits |
Number
of nets |
Breeding season
monitored? |
| UK |
1983 |
120 |
12 |
6-12 |
Yes |
| Finland |
1987 |
35 |
12 |
6-20 |
Yes |
| France |
1989 |
30 |
3 |
15-50 |
Early part only |
| Spain (SYLVIA) |
1991 |
38 |
10 |
7-15 |
Yes |
| The Netherlands |
1994 |
51 |
12 |
6-12 |
Yes |
| Spain (PASSER) |
1995 |
46 |
10 |
2-13 |
Yes |
| Sweden |
1996 |
29 |
12 |
3-15 |
Yes |
| Germany (Hiddensee) |
1997 |
26 |
12 |
2-11 |
Yes |
| Poland |
1999 |
10 |
12 |
8-10 |
Yes |
| Germany |
1999 |
35 |
12 |
6-20 |
Yes |
| Belgium |
2002 |
N.A. |
N.A. |
N.A. |
N.A. |
| Italy |
2002 |
19 |
N.A. |
N.A. |
N.A. |
| Portugal |
2002 |
10 |
N.A. |
N.A. |
N.A. |
| Czech Republic |
2003 |
1 |
9 |
N.A. |
N.A. |
Commonly caught species by constant effort ringing programmes in
Europe.
| Britain
& Ireland |
Spain |
France |
Finland |
Poland |
Sweden |
The Netherlands |
| Acrocephalus scirpaceus |
Acrocephalus scirpaceus |
Acrocephalus scirpaceus |
Acrocephalus schoenobaenus |
Acrocephalus scirpaceus |
Phylloscopus trochilus |
Acrocephalus scirpaceus |
| Acrocephalus schoenobaenus |
Sylvia atricapilla |
Sylvia communis |
Sylvia communis |
Acrocephalus palustris |
Erithacus rubecula |
Acrocephalus schoenobaenus |
| Sylvia
atricapilla |
Cettia
cetti |
Sylvia
borin |
Sylvia
borin |
Acrocephalus schoenobaenus |
Acrocephalus scirpaceus |
Sylvia
atricapilla |
| Phylloscopus trochilus |
Luscinia megarhynchos |
Sylvia atricapilla |
Phylloscopus trochilus |
Sylvia communis |
Sylvia atricapilla |
Phylloscopus trochilus |
| Parus caeruleus |
Hirundo rustica |
Hippolais polyglotta |
Ficedula hypoleuca |
Sylvia
atricapilla |
Turdus merula |
Troglodytes troglodytes |
| Troglodytes troglodytes |
Serinus serinus |
Luscinia megarhynchos |
Fringilla coelebs |
Sylvia
curruca |
Sylvia communis |
Turdus
merula |
| Prunella modularis |
Passer domesticus |
Phylloscopus collybita |
Parus
major |
Sylvia
borin |
Fringilla coelebs |
Emberiza schoeniclus |
| Fringilla coelebs |
Carduelis chloris |
Turdus
merula |
Parus caeruleus |
Phylloscopus trochilus |
Parus
major |
Parus
caeruleus |
| Turdus
merula |
Carduelis carduelis |
Erithacus rubecula |
Emberiza schoeniclus |
Parus
major |
Sylvia
borin |
Parus
major |
| Pyrrhula pyrrhula |
Turdus
merula |
Parus
major |
Turdus
iliacus |
Turdus
merula |
Emberiza schoeniclus |
|
|