The mallard (Anas platyrhynchos) is a focal species in game management, epidemiology and ornithology, but comparably little research has focused on the ecology of the migration seasons. We studied habitat use, time-budgets, home-range sizes, habitat selection, and movements based on spatial data collected with GPS devices attached to wild mallards trapped at an autumn stopover site in the Northwest European flyway. Sixteen individuals (13 males, 3 females) were followed for 15-38 days in October to December 2010. Forty-nine percent (SD = 8.4%) of the ducks' total time, and 85% of the day-time (SD = 28.3%), was spent at sheltered reefs and bays on the coast. Two ducks used ponds, rather than coast, as day-roosts instead. Mallards spent most of the night (76% of total time, SD = 15.8%) on wetlands, mainly on alvar steppe, or in various flooded areas (e.g. coastal meadows). Crop fields with maize were also selectively utilized. Movements between roosting and foraging areas mainly took place at dawn and dusk, and the home-ranges observed in our study are among the largest ever documented for mallards (mean = 6,859 ha; SD = 5,872 ha). This study provides insights into relatively unknown aspects of mallard ecology. The fact that autumn-staging migratory mallards have a well-developed diel activity pattern tightly linked to the use of specific habitats has implications for wetland management, hunting and conservation, as well as for the epidemiology of diseases shared between wildlife and domestic animals.

The last decade has seen a surge in research on avian influenza A viruses (IAVs), in part fuelled by the emergence, spread and potential zoonotic importance of highly pathogenic virus subtypes. The mallard (Anas platyrhynchos) is the most numerous and widespread dabbling duck in the world, and one of the most important natural hosts for studying IAV transmission dynamics. In order to predict the likelihood of IAV transmission between individual ducks and to other hosts, as well as between geographical regions, it is important to understand how IAV infection affects the host. In this study, we analysed the movements of 40 mallards equipped with GPS transmitters and three-dimensional accelerometers, of which 20 were naturally infected with low pathogenic avian influenza virus (LPAIV), at a major stopover site in the Northwest European flyway. Movements differed substantially between day and night, as well as between mallards returning to the capture site and those feeding in natural habitats. However, movement patterns did not differ between LPAIV infected and uninfected birds. Hence, LPAIV infection probably does not affect mallard movements during stopover, with high possibility of virus spread along the migration route as a consequence.

Background: Chlamydia psittaci is an intracellular bacterium primarily causing respiratory diseases in birds but may also be transmitted to other animals, including humans. The prevalence of the pathogen in wild birds in Sweden is largely unknown. Methods: DNA was extracted from cloacae swabs and screened for C. psittaci by using a 23S rRNA gene PCR assay. Partial 16S rRNA and ompA gene fragments were sequence determined and phylogenies were analysed by the neighbour-joining method. Results and conclusion: The C. psittaci prevalence was 1.3% in 319 Peregrine Falcons and White-tailed Sea Eagles, vulnerable top-predators in Sweden. 16S rRNA and ompA gene analysis showed that novel Chlamydia species, as well as novel C. psittaci strains, are to be found among wild birds.

1. Understanding drivers of variation and trends in biodiversity change is a general scientific challenge, but also crucial for conservation and management. Previous research shows that patterns of increase and decrease are not always consistent at different spatial scales, calling for approaches combining the latter. We here explore the idea that functional traits of species may help explaining divergent population trends.
2. Complementing a previous community level study, we here analyse data about breeding waterbirds on 58 wetlands in boreal Fennoscandia, covering gradients in latitude as well as trophic status. We used linear mixed models to address how change in local abundance over 25 years in 25 waterbird species are associated with life history traits, diet, distribution, breeding phenology, and habitat affinity.
3. Mean abundance increased in 10 species from 1990/1991 to 2016, whereas it decreased in 15 species. Local population increases were associated with species that are early breeders and have small clutches, an affinity for luxurious wetlands, an herbivorous diet, and a wide breeding range rather than a southern distribution. Local decreases, by contrast, were associated with species having large clutches and invertivorous diet, as well as being late breeders and less confined to luxurious wetlands. The three species occurring on the highest number of wetlands all decreased in mean abundance.
4. The fact that early breeders have done better than late fits well with previous research about adaptability to climate change, that is, response to earlier springs. We found only limited support for the idea that life history traits are good predictors of wetland level population change. Instead, diet turned out to be a strong candidate for an important driver of population change, as supported by a general decrease of invertivores and a concomitant increase of large herbivores.
5. In a wider perspective, future research needs to address whether population growth of large‐bodied aquatic herbivores affects abundance of co‐occurring invertivorous species, and if so, if this is due to habitat alteration, or to interference or exploitative competition.

Breeding success in ground-nesting birds is primarily determined by nest survival, which may be density-dependent, but the generality of this pattern remains untested. In a replicated crossover experiment conducted on 30 wetlands, survival of simulated mallard nests was related to "biome" (n=14 mediterranean and 16 boreal wetlands), breeding "phenology" (early vs late nests), and "density" (2 vs 8 nests per 225 m shoreline). Local abundances of "waterfowl", "other waterbirds", and "avian predators" were used as covariates. We used an information-theoretic approach and Program MARK to select among competing models. Nest survival was lower in late nests compared with early ones, and it was lower in the mediterranean than in the boreal study region. High-density treatment nests suffered higher depredation rates than low-density nests during days 1-4 of each experimental period. Nest survival was negatively associated with local abundance of "waterfowl" in the boreal but not in the mediterranean biome. Effect estimates from the highest-ranked model showed that nest "density" (d 1-4) had the strongest impact on model fit; i.e. three times that of "biome" and 1.5 times that of "phenology". The latter's effect, in turn, was twice that of "biome". We argue that our study supports the idea that density-dependent nest predation may be temporally and spatially widespread in waterfowl. We also see an urgent need for research of how waterfowl nesting phenology is matched to that of prey and vegetation.

Häckningen är en känslig och farlig fas i fåglarnas årliga cykel. Många rovdjur utgör ett hot mot ägg och ungar. Viltforskare vid Högskolan Kristianstad berättar här om nya rön om samspelet mellan gräsänder och de rovdjur som rövar deras bon.

Breeding success in many birds including wildfowl is mainly determined by nest predation. Few studies address cues used by predators to find duck nests, and the same is true for spacing patterns that ducks might use to reduce predation. We designed a crossover experiment in agricultural and forested settings to test the assumption that nest predation rate is related to density of adult birds on a lake. We used introduced wing-clipped mallards (Anas platyrhynchos L., 1758) to increase local pair density and semi-natural nests to assess predation rate. Depredation patterns were analyzed by model fitting in program MARK, using introduction and landscape type as main effects and abundance of avian predators and wild waterbirds as covariates. Depredation was higher at agricultural lakes than at forest lakes. Nest survival decreased with increasing abundance of wild waterfowl, whereas it tended to increase with the abundance of "other waterbirds". There was a landscape-dependent effect of increased mallard pair density: positive at agricultural lakes and negative at forest lakes. Avian predators found 91% of depredated "known-predator" nests at agricultural lakes and 25% at forest lakes; mammals found 9% at agricultural lakes and 75% at forest lakes. The landscape-dependent density effect may in part be due to different predator communities in these landscape types.

Häckningen är på många sätt den viktigaste delen av fåglarnas årscykel, men den är också en av de farligaste.

Ett bo fullt med ägg är ju en fantastisk måltid för många rovdjur. mFågelekologer vid Högskolan Kristianstad berättar här om nya rön om samspelet mellan gräsänder och de rovdjur som gillar deras bon. Det finns mycket att vinna för de änder som häckar vid rätt tidpunkt och placerar sina bon på rätt ställe!

Breeding success in wild mallards was studied on small eutrophic nemoral lakes in a two-year cross-over experiment in which wing-clipped conspecifics were added to increase pair density. The number of wild mallards that came to the lakes to nest (prior to introductions) did not differ between years. Introduction treatment led to a significant reduction in brood number in wild mallards, but it did not alter the number of stage 2+ ducklings finally produced on a lake. Introduction had no effect on lake utilization by broods, ducklings and non-breeding adults (cumulative days over the entire breeding season). Abundance of invertebrate prey differed greatly among lakes, but it did not correlate with breeding success. Breeding success was thus subject to sequential density-dependence; i.e. a lower number of broods still produced the same number of 2+ ducklings. We speculate that predation is the most likely process behind both patterns. We conclude that late and snapshot measures of duckling productivity may mask density dependent population processes of fundamental importance to regulation and harvest policy.

Density dependence in vital rates is a key issue in population ecology but remains largely unexplored experimentally. We studied breeding success, lake use, and prey availability in wild mallards Anas platyrhynchos on small nemoral lakes in a replicated, two-year cross-over experiment in which pair density was increased. The number of wild mallards that settled on lakes prior to introductions of extra pairs did not differ between control and introduction years. Introductions led to a lake-level reduction in the number of broods observed. However, the number of stage 2/ (almost fledged) ducklings did not differ between treatments, nor did lake utilization by nonbreeding adults, broods and ducklings. Prey resource availability differed greatly among lakes, but it did not correlate with breeding success. Partialling out the possible effect of food competition from wild adult nonbreeding mallards did not change this conclusion. Our study demonstrates sequential density dependence in breeding success; introductions caused a decrease in brood number, but despite fewer broods a similar number of nearly fledged ducklings were produced. We suggest that predation and/or lake change of broods soon after hatching created these patterns. We conclude that using a single and late measure of breeding success such as fledged birds can mask regulatory processes. Implications of density dependence and its relation to individual reproductive success are understood better if breeding success is decomposed into nest success, duckling survival and fledgling survival.

Density dependence in vital rates is a key issue in population ecology but remains largely unexplored experimentally. We studied breeding success, lake use, and prey availability in wild mallards Anas platyrhynchos on small nemoral lakes in a replicated, two-year cross-over experiment in which pair density was increased. The number of wild mallards that settled on lakes prior to introductions of extra pairs did not differ between control and introduction years. Introductions led to a lake-level reduction in the number of broods observed. However, the number of stage 2+ (almost fledged) ducklings did not differ between treatments, nor did lake utilization by nonbreeding adults, broods and ducklings. Prey resource availability differed greatly among lakes, but it did not correlate with breeding success. Partialling out the possible effect of food competition from wild adult nonbreeding mallards did not change this conclusion. Our study demonstrates sequential density dependence in breeding success; introductions caused a decrease in brood number, but despite fewer broods a similar number of nearly fledged ducklings were produced. We suggest that predation and/or lake change of broods soon after hatching created these patterns. We conclude that using a single and late measure of breeding success such as fledged birds can mask regulatory processes. Implications of density dependence and its relation to individual reproductive success are understood better if breeding success is decomposed into nest success, duckling survival and fledgling survival.

Teal (Anas crecca) broods were studied in 1988-2003 in a boreal watershed comprising 51 permanent wetlands. Brood size of near-fledged ducklings was negatively related to the hatching date, i.e. early pairs had higher reproductive success than late pairs. However, brood size of newly hatched ducklings was not related to the hatching date, implying that the advantage of early breeding is due to processes operating during the brood stage rather than during nesting. Half of the lakes never produced a brood, and among the 26 lakes that actually did, two `preferred' lakes generated 44% of the broods and 55% of the near-fledged ducklings. Early broods were over-represented on such `preferred' lakes, and late broods over-represented on `less preferred' lakes. Our study suggests that lake selection and early nesting may have important fitness consequences in teal.

It is an axiom in ecology that knowing the sheer number of individuals in a population is of very little help if the objective is to understand future and past changes in population size. Yet, this is exactly how migratory European ducks are monitored, many of which are important quarry species in several countries. We argue that present monitoring is insufficient to address objectives of wise use and sustainability such as those emphasised in recent management directives and multilateral international agreements. The two main problems are the almost total lack of reliable data on recruitment and mortality. We advocate a pan-European monitoring system based on undisputed scientific principles; i.e. a long-term, coordinated and standardised scheme that produces data about vital rates of duck populations as well as about harvest size. Data from such a scheme can be used by game biologists to produce predictive tools, thus providing a functional basis for management decisions for adaptive harvesting and conservation alike.

The practice of restocking already viable populations to increase harvest potential has since long been common in forestry, fisheries and wildlife management. The potential risks of restocking native species have long been overshadowed by the related issue of invasive alien species. However, during the last decade releases of native species with potentially non-native genome have received more attention. A suitable model to study genetic effects of large-scale releases of native species is the Mallard Anas platyrhynchos, being the most widespread duck in the world, largely migratory, and an important quarry species. More than 3 million unfledged hatchlings are released each year around Europe to increase local harvest. The aims of this study were to determine if wild and released farmed Mallards differ genetically, if there are signs of previous or ongoing introgression between wild and farmed birds, and if the genetic structure of the wild Mallard population has changed since large-scale releases started in Europe in the 1970s. Using 360 Single Nucleotide Polymorphisms (SNPs) we found that the genetic structure differed among historical wild, present-day wild, and farmed Mallards in Europe. We also found signs of introgression in the wild Mallard population, that is, individuals with a genetic background of farmed stock are part of the present free-living population. Although only a small proportion of the released Mallards appears to survive to merge with the free-living breeding population, their numbers are still so large that the genetic impact may have significance for the wild population in terms of individual survival and longterm fitness.

Influenza A virus (IAV) has its natural reservoir in wild waterfowl and emerging human IAVs often contain gene segments from avian viruses. The active drug metabolite of oseltamivir (oseltamivir carboxylate (OC)), stockpiled as Tamiflu® for influenza pandemic preparedness, is not removed by conventional sewage treatment and has been detected in river water. There, it may there exert evolutionary pressure on avian IAV in waterfowl, resulting in development of resistant viral variants. A resistant avian IAV can circulate among wild birds only if resistance does not restrict viral fitness and if the resistant virus can persist without continuous drug pressure. In this in vivo Mallard (Anas platyrhynchos) study we tested if an OC-resistant avian IAV strain (A(H1N1)/NA-H274Y) could retain resistance while drug pressure was gradually removed. Successively infected Mallards were exposed to decreasing levels of OC, and fecal samples were analyzed for neuraminidase sequence and phenotypic resistance. No reversion to wild-type virus was observed during the experiment, which included 17 days of viral transmission in 10 ducks exposed to OC concentrations below resistance induction levels. We conclude that resistance in avian IAV, induced by OC exposure of the natural host, can persist in absence of the drug. Thus, there is a risk that human pathogenic IAVs that evolve from IAVs circulating among wild birds may contain resistance mutations. An oseltamivir resistant pandemic IAV would be a substantial public health threat. Therefore, our observations underscore the need for prudent oseltamivir use, upgraded sewage treatment and resistance surveillance of IAV in wild birds.

The consequences of climate change for bird populations have received much attention in recent decades, especially amongst cavity-nesting songbirds, yet little has been written on ducks (Anatidae) despite these being major elements of wetland diversity and important quarry species. This paper reviews the major known consequences of climate change for birds in general, and relates these to the limited information available specifically for ducks. Climate change can influence migration distance and phenology, potentially affecting patterns of mortality, as well as distribution and reproductive success in ducks. Studies addressing effects of climate change are, however, restricted to very few duck species, including mallardAnas platyrhynchos and common eider Somateria mollissima. Shifts in winter duck distributions have been observed, whereas the mismatch hypothesis (mistiming between the periods of peak energy requirements for young and the peak of seasonal food availability) has received limited support with regard to ducks. We propose a range of monitoring initiatives, including population surveys, breeding success monitoring schemes and individual duck marking, which should later be integrated through population modelling and adaptive management to fill these gaps.

It is unresolved to what extent waterfowl populations are regulated by density-dependent processes. By doing a 2-year crossover perturbation experiment on ten oligotrophic boreal lakes we addressed the hypothesis that breeding output is density dependent. Wing-clipped mallard (Anas platyrhynchos) hens were introduced with their own brood and then monitored for 24 days. Predicted responses were that per capita duckling and hen survival would be lower in high-density than in low-density treatments. Survival was evaluated by model fitting in program MARK. Density, year, and lake were used as main effects, while day after introduction, a weather harshness index, and presence of hens were covariates. Daily survival in ducklings was lower in the high-density treatment, but this effect was year dependent. The highest-ranking model for duckling survival also included a positive effect of duckling age and presence of hens, and a negative effect of harsh weather. Density did not affect female survival although there was a prominent year effect. The highest-ranking model for female survival also included negative effects of day after introduction and harsh weather. This is the first study to report density-dependent survival in experimentally introduced ducklings in a natural setting. Implications for population dynamics and management of harvested populations are far-reaching if such regulation occurs in some years, but not in others.

På relativt kort tid har flera arter strandängsvadare minskat dramatiskt i Kristianstads Vattenrike. Pågående forskning bedrivs för att utröna om nedgångarna kan ha orsakats av faktorer längre ner i näringsväven. I speciellt fokus för forskningen är produktionen av vegetation och ryggradslösa djur.

Measuring and assessing vital rates such as births and deaths are prerequisites for understanding population dynamics. Vital rates may be affected by the density of individuals, even though the importance of density dependence on population dynamics has been debated for a long time. The mallard Anas platyrhynchos is one of the foremost game species in the Holarctic, with millions of birds in hunters’ bags annually. Still, basic knowledge about regulation of mallards’ vital rates is poor, and experimental studies on this topic are rare.

In this thesis I have studied survival patterns and density dependence in mallards breeding in Sweden and Finland. Long-term ringing data from both countries were analysed for mortality patterns and causation, as well as for e.g. survival rate estimation. Most of the studies were, though, experiments run over two years involving manipulations of the density of nests, broods and/or adults, in southern and northern Sweden, comprising different biotic regions. Common response variables were survival of nests, ducklings and hens, mainly analysed with program MARK.

About 90% of the recovered mallards in Finland and Sweden were hunting kills. However, survival rates were high, ranging from 0.66 to 0.81 for most groups (sex*age). The generality of density dependence was evident since such processes were detected in all studies. Consequently, depredation rate was higher in high nest density compared to low nest density. Survival of ducklings was density-dependent in both boreal and nemoral biotic regions, with food limitation being evident in the former region but not in the latter. In spite of their generality, density-dependent patterns varied within as well between years, and for nest predation rates also between landscape types.

The findings about density dependence in breeding mallards in this thesis are novel since they are based on experiments. They are potentially of general interest for management because they embrace a variety of lakes in two geographically distant areas, each being representative for large temperate areas in the northern hemisphere. Detection of density dependence at the local scale may be important at larger scales, too, following the principle of ‘ideal preemptive distribution’ in a source-sink dynamic system.

Breeding success is a key element of animal population dynamics. In many taxa including birds, nest success, or the proportion of laid clutches that actually hatch, is mainly determined by predation. Previous research gives an inconsistent picture of the prevalence of density-dependent nest predation and one reason for this is the general lack of well-designed replicated experiments. Using simulated Mallard Anas platyrhynchos nests and a crossover design for 20 lakes in the nemoral and boreal biotic zones, we tested the predictions that nest survival is negatively density-dependent and that nest predation is higher in agricultural than in forested landscapes. Study day and daily abundance of waterfowl, other waterbirds, as well as avian predators were included as covariates in the analysis. Model fitting in program mark revealed a general negative effect of nest density on nest survival. In addition, nest survival rate was higher at forest lakes than at lakes in agricultural landscapes, irrespective of nest density. The only covariate producing model improvement was study day; older nests had higher survival rates than recently initiated ones. This is the first replicated lake-level experimental study showing that nest predation is density-dependent in waterfowl. The pattern was consistent between landscape types, implying that density-dependent nest predation may affect habitat choice and population dynamics over large parts of the Mallard's range.

Ecological theory frequently postulates that most animal species are subject to density-dependent mechanisms in some stage of the year or life. However, few avian studies have succeeded to give evidence for regulatory mechanisms by replicated experiments in natural habitats. Breeding success is to a great extent determined by conditions during the nesting period and the major cause of nesting failure is nest predation. In addition, predators may possibly regulate fluctuating populations and to test the hypothesis that nest survival is negatively density-dependent we conducted an experiment with manipulated densities of semi-natural Mallard nests and adult pairs using 32 small to medium sized lakes (~3-5 hectares) in southern Sweden during two nesting seasons (2003-2004). Predicting that predation rates are higher in open compared to more vegetated habitats, half of the lakes were in agricultural and the other half in forest landscapes. Using real Mallard eggs, nests were constructed in two densities; either 2 nests per lake (low density) or 8 nests per lake (high density). Model fitting in program MARK revealed that nest survival was negatively affected by nest density but not by pair density. Further, predation rates were much higher in agricultural landscapes than in forested. The effects of nest density and habitat were consistent in the two years. Covariates added to the model matrix revealed a negative effect of other waterfowl present on the lakes and a positive effect of study day. However, the number of avian predators observed at the lakes did not affect survival. Our experiment is the first to demonstrate density-dependent nest predation in Mallard. The consistency of the density effect between years and habitats shows that regulatory mechanisms may be truly significant for Mallard, possibly affecting population dynamics of the species.

Long-term mallard capture-recapture data from Sweden and Finland were analyzed to describe temporal mortality patterns and reasons. We used program MARK and Seber models to estimate annual survival (S) and recovery (r) rates. Survival rates were used in a Monte Carlo simulation to evaluate the correspondence between observed and predicted annual population sizes of a Finnish sub-population. About 90% of recovered birds died from hunting. Most recoveries were from the hunting season, and more males than females were shot. Predation was the most common cause of natural mortality. Finnish capture-recapture data fitted best the global model in which survival and recovery vary with age and sex. Annual survival and recovery rates for adult and juvenile males and females were overlapping, ranging from 0.46 to 0.90 (survival) and 0.07 to 0.17 (recovery), whereas pulli had lower survival rates (0.21-0.42). Pulli that were successfully sexed at the time of ringing had higher recovery rates (female pulli: 0.23; male pulli: 0.32) than juveniles and adults. Density-dependent fledgling production was detected in the Finnish sub-population and was accounted for in the Monte Carlo simulation, which estimated predicted breeding population size quite well, although one of the observed annual values (2003) fell outside the 95% confidence limits.

Density dependence (DD) is a central concept in population ecology and in the management of harvested populations. For example, DD underpins the idea of additive versus compensatory mortality and is a tenet in the paradigm of resource limitation and regulation. Yet the prevalence and importance of DD remains disputed in most organisms, including ducks, which are focal in game management, conservation and zoonotic diseases. Based on 154 data entries from 54 studies in the peer-reviewed literature, we here synthesize and evaluate the prevalence of DD in breeding ducks in relation to (1) species and guild (dabbling versus diving ducks), (2) stage in the breeding cycle (nesting, duckling, recruitment) or, alternatively, in terms of population dynamics, (3) study type (descriptive/nonmanipulative versus experimental), (4) continent (Europe versus North America), (5) spatial level (wetland, landscape, regional, continental) and (6) biome (tundra, boreal, nemoral, prairie, mediterranean). One conclusion from this review is that it is difficult to find general patterns about the prevalence of DD unless data are broken down to subsets, for example, to stage or spatial level. With respect to stage, DD effects occur at all stages of the breeding cycle. During the nesting and duckling stages, the frequency of cases detecting versus not detecting DD is roughly the same. However, in cases referring to the recruitment stage, i.e. to survival of fledged ducks until 1 year old at the most, DD was the rule, suggesting that DD processes may operate mainly outside the breeding season. Further subdivision of data shows that spatial scale is important to the prevalence of DD in nesting ducks—rare on the wetland level and more common on higher spatial levels. In studies of population dynamics (i.e. based on time series data only), DD was more often found in diving than in dabbling ducks. This corroborates previous suggestions that dabbling ducks largely should be considered as r-selected species, in contrast to more K-selected diving ducks, which start to reproduce at an older age and often breed in more stable wetland environments where resources may be easier to track and populations thus often are closer to carrying capacity. However, the picture of DD in ducks is far from complete, and knowledge gaps for future studies to address include: (a) data from Russia, which holds a large part of the breeding ducks in the Northern hemisphere, (b) experimental studies on more species to separate density-dependent factors from other drivers of population change and to tease apart spatial and temporal interactions in the underlying processes, (c) time series analyses addressing population dynamics, especially from outside North America, (d) studies relating duck numbers to limiting resources, which arguably is the most relevant measure of density, (e) the timing of DD processes in relation to harvest and natural mortality.

It is unresolved to what extent waterfowl populations are regulated by density-dependent pro cesses. By doing a 2-year crossover perturbation exper iment on ten oligotrophic boreal lakes we addressed the hypothesis that breeding output is density depen dent. Wing-clipped mallard (Anas platyrhynchos) hens were introduced with their own brood and then moni tored for 24 days. Predicted responses were that per capita duckling and hen survival would be lower in high-density than in low-density treatments. Survival was evaluated by model fitting in program MARK. Density, year, and lake were used as main effects, while day after introduction, a weather harshness index, and presence of hens were covariates. Daily survival in ducklings was lower in the high-density treatment, but this effect was year dependent. The highest-ranking model for duckling survival also included a positive effect of duckling age and presence of hens, and a nega tive effect of harsh weather. Density did not affect female survival although there was a prominent year effect. The highest-ranking model for female survival also included negative effects of day after introduction and harsh weather. This is the first study to report den sity-dependent survival in experimentally introduced ducklings in a natural setting. Implications for population dynamics and management of harvested populations are far-reaching if such regulation occurs in some years, but not in others.

During the breeding period dabbling ducks (Anas sp.), and especially newly hatched ducklings, face heavy mortality. The reasons are not clear, but suggested factors contributing are scarce food, predation, chilling and disease. We highlighted the question why many of the boreal lakes in Scandinavia are without breeding ducks and why mortality is considerable during brood period. In an experimental study in 2002 we hypothesized food being a major factor deciding duck survival during breeding. One wing-clipped hen mallard with her own newly hatched brood (10 ducklings) was introduced onto each of 10 lakes. Food was added ad libitum at 5 of these lakes (experimental lakes), whereas the other five lakes (controls) did not get any extra food added. Survival of hens, broods as well as each individual duckling was monitored regularly until 24 days after introduction. At all three levels (i.e. duckling, brood and adult), survival was significantly higher on lakes with food added than on control lakes, although the difference was most pronounced on the duckling level. Direct consequences (i.e. dying from starvation) as well as indirect (e.g. undernourished individuals being more easily taken by predators) may both explain this pattern. Our results clearly show that food is a major limiting factor on mallard survival in this environment. Also, our results may explain why many boreal lakes in Scandinavia do not have any breeding waterfowl at all. It seems likely that such lakes are too poor to raise broods and even to sustain adults.

Food is an important factor affecting survival in many bird species, but this relationship has rarely been explored experimentally with respect to reproductive output of precocial birds. In a field experiment we tested the hypothesis that food abundance limits reproductive output in breeding dabbling ducks. Onto 10 oligotrophic lakes in northern Sweden we introduced one wing-clipped female mallard (Anas platyrhynchos L., 1758) and a brood of 10 newly hatched ducklings, and survival was monitored for 24 days. Food was added ad libitum at five of the lakes, but not at the other five. Duckling survival was best modelled to include a treatment effect, with higher survival on lakes with food added, and a negative effect of harsh weather. As expected, duckling survival increased nonlinearly with age. Only one female remained on control lakes after 24 days, whereas four remained on lakes with food added. This is the first experimental demonstration that food may limit survival and reproductive output in breeding precocial birds. We argue that food limitation may be one reason why duckling mortality is high and why many lakes throughout the Holarctic have no breeding dabbling ducks.

The shorebird community has decreased dramatically along the lower parts of the ‘Helge å’ river in "Kristianstads Vattenrike" in recent years. Causes are not clear, but a number of possible factors have been suggested. This report presents studies carried out in 2012, and aimed to investigate two of these factors, i.e. (1) food abundance (i.e. invertebrates) with possible links to the summer flooding in 2007, and (2) if there is any support in weather and hydrological data that springs have become drier.

Food abundance was generally high on the meadows. However, in wetlands (wet pools, "Helge å", "Hammarsjön") there were differences between study sites, with more abundant prey downstream in the "Helge å" river system as contrasted to upstream sites. This may be a consequence of the summer flooding in 2007.

There were no clear signs that springs have become direr from 1990 to 2012, as judged by weather and hydrological data. One could possibly argue that most springs in the early 1990s and in the last 10 years were drier than what is normal as opposed to wetter springs in the late 1990s. Still, with the data at hand it is not possible to make any accurate conclusions about long-term trends and how such have affected the habitats and the breeding success of shorebirds.

To prevent the shorebird community from further declines, and instead turn the population trends to become positive, drastic and immediate actions must be implemented. These must focus on reducing the (1) grazing pressure of meadows, (2) predation pressure on eggs and chicks of waders, and (3) dehydration of wet pools.