Radio-telemetry observations of the first 650 km of the migration of Bar-tailed Godwits Limosa lapponica from the Wadden Sea to the Russian Arctic

In 1999 and 2000, 45 Bar-tailed Godwits Limosa lapponica were supplied with radio-transmitters during spring staging on the island Texel in the western Wadden Sea. With the use of Automatic Radio Tracking Stations (ARTS) on Texel and in south Sweden, and hand-held receivers on Texel, it was possible to follow the later part of the stopover period on Texel for 34 birds (76%) and the passage over south Sweden for 26 birds (58%). Thus, the method of automatic tracking of overflying migrating shorebirds works successfully where the migration corridor is narrow and predictable, as in the case with late spring shorebird migration from the Wadden Sea towards arctic Russia. The timing of departure from Texel and passage over south Sweden of radio-marked birds, with median dates of 30 May and 2 June respectively, were in agreement with published data on the spring migration of Siberian-breeding Bar-tailed Godwits L. l. taymyrensis. The individual variation in migration dates was larger than expected, with birds passing south Sweden between 25 May and 10 June, indicating that the time-window for departure might be broader than previously thought. There was no clear difference between males and females in timing of migration. The time difference between departure from Texel and passage over south Sweden (average 3.3 days) indicates that most Bar-tailed Godwits do not embark on the long flight towards Siberia directly from the western Wadden Sea, but are more likely to stop in the more easterly portion of the Wadden Sea before the final take-off. This pattern is similar to what has been found in other shorebirds and geese (e.g. Red Knots Calidris canutus and Dark-bellied Brent Geese Branta bernicla) migrating along the same route.

Do Red Knots (Calidris Canutus Islandica) routinely skip Iceland during southward migration?

Subspecies Calidris canutus islandica of the Red Knot breeds on the arctic tundra of northeastern Canada and northern Greenland and winters along the coasts of northwestern Europe. During northward migration, it stops over in either Iceland or northern Norway. It has been assumed that it does the same during southward migration. Using ratios of stable carbon isotopes (&delta; 13 C) in whole blood, blood cells, and plasma, we investigated evidence for a stopover in Iceland en route from the breeding grounds to the Dutch Wadden Sea. With the expected diet (shellfish) and stopover duration at Iceland (12-15 days, maximum 17 days) and the turnover rates of blood cells (15.1 days) and plasma (6.0 days), Red Knots that stopped in Iceland should arrive with a blood (cell) &delta; 13 C midway between a tundra (-24.7[per thousand]) and a marine value (-14.0[per thousand]) and a plasma &delta;13 C approaching the marine value (-15.3[per thousand]). However, many adults arriving at the Wadden Sea had &delta;13 C ratios in blood (cells) and plasma below these levels, and some arrived with clear tundra signals in blood cells, suggesting that they skipped Iceland during southward migration. Surprisingly, available data suggest this also to be true for juveniles during their first southward migration. The &delta; 13 C signature of second-year birds confirmed that they oversummered in the Wadden Sea. Our findings contradict the largely untested idea that juvenile shorebirds make more stopovers than adults as well as the idea that the migration between the Nearctic and Europe is necessarily a two-leg process. <br /

Grote aantallen Drieteenstrandlopers uit allerlei windstreken bij Griend, nazomer 2011

De wadplaten van de Waddenzee zijn van groot belang voor trekkende steltlopers. Ze tanken er bij op weg naar de broedgebieden in het voorjaar en de overwinteringslocaties in het najaar (o.a. Boere 1977, van de Kam et al. 1999, Reneerkens et al. 2005). Sommige soorten steltlopers die door de Waddenzee trekken, zoals Kanoeten Calidris canutus en Rosse Grutto’s Limosa lapponica, overwinteren massaal in slechts enkele gebieden: de Banc d’Arguin in Mauritanië en de Bíjagos archipel in Guinee-Bissau. In contrast daarmee strekt het overwinteringsgebied van Drieteenstrandlopers Calidris alba, Steenlopers Arenaria interpres en Bontbekplevieren Charadrius hiaticula zich uit langs de hele kust van West-Europa en de westkust van Afrika (Delany et al. 2009). Maar waar komen de in de Waddenzee doortrekkende Drieteenstrandlopers vandaan en waar gaan ze naar toe? De afgelopen jaren zijn veel Drieteenstrandlopers op allerlei locaties langs de Oost-Atlantische trekroute individueel herkenbaar gemaakt met behulp van kleurringen (Reneerkens et al. 2009a). Hierdoor konden we inzicht verkrijgen in de herkomst en bestemming van de Drieteenstrandlopers die in de nazomer van 2011 rond het eiland Griend in de centrale Nederlandse Waddenzee pleisterden. Daarnaast konden we op basis van de fractie gekleurringde vogels een schatting maken van het aanwezige aantal

Shellfish Dredging Pushes a Flexible Avian Top Predator out of a Marine Protected Area

There is a widespread concern about the direct and indirect effects of industrial fisheries; this concern is particularly pertinent for so-called “marine protected areas” (MPAs), which should be safeguarded by national and international law. The intertidal flats of the Dutch Wadden Sea are a State Nature Monument and are protected under the Ramsar convention and the European Union's Habitat and Birds Directives. Until 2004, the Dutch government granted permission for ~75% of the intertidal flats to be exploited by mechanical dredgers for edible cockles (Cerastoderma edule). Here we show that dredged areas belonged to the limited area of intertidal flats that were of sufficient quality for red knots (Calidris canutus islandica), a long-distance migrant molluscivore specialist, to feed. Dredging led to relatively lower settlement rates of cockles and also reduced their quality (ratio of flesh to shell). From 1998 to 2002, red knots increased gizzard mass to compensate for a gradual loss in shellfish quality, but this compensation was not sufficient and led to decreases in local survival. Therefore, the gradual destruction of the necessary intertidal resources explains both the loss of red knots from the Dutch Wadden Sea and the decline of the European wintering population. This study shows that MPAs that do not provide adequate protection from fishing may fail in their conservation objectives

Individual shifts toward safety explain age-related foraging distribution in a gregarious shorebird

Although age-related spatial segregation is ubiquitous, the underlying mechanisms are poorly understood. Here, we aim to elucidate the processes behind a previously established age-related foraging distribution of red knots (Calidris canutus canutus) in their main wintering area in West Africa (Banc d’Arguin, Mauritania). Based on 10 years of observations of 1232 uniquely color-ringed individuals of 1 to 18+ years old, we examined whether the observed age-related foraging distribution resulted from 1) spatial differences in mortality or 2) age-related shifts in habitat use. Using multistate capture–recapture modeling, we showed that with age foraging red knots moved away from the shoreline, that is, to areas with fewer surprise attacks by raptors. Considering uncertainties in the subjective gradient in predation danger with increasing distance from shore (as assessed from correlations between vigilance and distance from shore in foraging birds), we applied 2 different danger zone boundaries, at 40 m and 500 m from shore. Between years, red knots had a much higher chance to move from the dangerous nearshore area to the “safe” area beyond (71–78% and 26% for 40-m and 500-m danger zone boundary, respectively), than vice versa (4% and 14%). For neither danger zone boundary value did we find differences in annual mortality for individuals using either dangerous or safe zone, so the move away from the shore with age is attributed to individual careers rather than differential mortality. We argue that longitudinal studies like ours will reveal that ontogenetic shifts in habitat use are more common than so far acknowledged