A wildfowler aiming a shotgun at sunset
A wildfowler aiming a shotgun at sunset

A code of practice for wildfowl quarry species

This code applies only in England, Wales, Scotland and Northern Ireland.

Introduction

To ensure the long-term future of shooting, it is essential that the shooting of wildfowl is sustainable.

Within this context, sustainable shooting respects quarry species and seeks to conserve and improve the environment. It avoids excessive consumption, complies with the law, improves the health and well-being of participants, and provides food and economic benefits to the wider community.

This code relates to the quarry species listed below, particularly those where the available evidence demonstrates the need for action.

Ducks

Gadwall
Goldeneye**
Mallard*
Scaup**1

Pintail**
Pochard**
Shoveler

Teal
Tufted duck
Wigeon

Geese

Canada goose
Greylag goose

Pink-footed goose
European white-fronted goose**2

Waders

Common snipe**
Golden plover
Jack Snipe1
Woodcock**

Rails

Coot**3
Moorhen**3

The ‘broad sustainability principles’ apply to all species, with the following variations.

a) * This code does not apply to reared and released mallard, and the shooting thereof.
b) ** Bespoke actions are required for these species; see species-specific recommendations.
c) 1 Northern Ireland only.
d) 2 England & Wales only.
e) 3 England, Wales, & Scotland only.
f) This code does not apply to the use of large bore historic firearms used to maintain historic, cultural and traditional aspects of wildfowling.
g) This code does not override any site-based requirements; all shooters need to abide by landowner, club, or consent restrictions.

It is important that those who shoot recognise that unsustainable shooting can affect population size, age composition, sex ratio, behaviour, and distribution of natural populations. Understanding the potential impacts of shooting is a prerequisite to managing quarry species in a sustainable manner.

The code provides advice at two levels:

  • Advice that must be followed in order to deliver sustainable shooting – unless otherwise stated the term ‘must’ only applies to meeting the standards set by this code of practice and does not refer to a legal obligation. 
  • Advice that should be followed in order to achieve best practice, any deviation from which would need justification.

This code of practice therefore captures the following aspects of sustainable shooting:

i) Broad sustainability principles that can be applied to the shooting of all quarry species listed within this code and should be followed by all participants.

ii) Individual quarry species recommendations regarding the taking of species where the evidence review highlights potential conservation impacts. The ‘shooting restrictions’ recommendations must be followed but will vary subject to available data and will be updated periodically.

iii) Practical recommendations whereby shooters can contribute to the conservation of individual quarry species through behaviour changes, data collection and facilitating practical conservation.

The following golden rules apply

  1. To ensure shooting is sustainable, those who shoot must adhere to the species-specific shooting recommendations. 
    a. Pochard – no take – targeted conservation effort required.
    b. Pintail – take a maximum of two birds per day – targeted conservation effort required.
    c. Woodcock – delay shooting until late November where resident woodcock are present.
    d. Scaup – show restraint, site-based considerations required.
    e. Goldeneye – delay shooting until October where resident goldeneye are present.
    f. European white-fronted goose – take a maximum of two birds per person, per day.
    g. Common snipe – delay shooting until 1 September where resident snipe are present.
  2. Eat what you shoot. It is your responsibility to ensure all shot quarry is put to good use.
  3. Where not already required by law, consent, or lease, shooters should collect bag data and submit information for all wildfowl species to a national monitoring scheme.
  4. Shooters should contribute to habitat creation, management, and restoration initiatives.
  5. Shooters should assist with citizen science initiatives including bird counts, ring recovery reporting, wing surveys, disease monitoring, etc.

Sustainability principles for all wildfowl, wader, and rail quarry species

Geese in flight

Shooting

Geese

a. Eat what you shoot. It is your responsibility to ensure all shot quarry is put to good use.
b. You must comply with any club or site-specific rules
or regulations, sector-specific codes and best practice guidance.
c. No more than six grey geese – to a maximum of five pinkfeet, four greylag, and two European white-fronts per person, per day – unless for conservation, health and safety, or crop protection measures (and supported by a licence agreement or management plan). At all times show restraint. Take what you need, not what you can.

Ducks, waders, and rails

a. Eat what you shoot. It is your responsibility to ensure all shot quarry is put to good use.
b. You must comply with any club or site-specific rules or regulations, sector-specific codes and best practice guidance.
c. No more than ten ducks per person, per day. At all times show restraint, Take what you need, not what you can.

Evidence and research

Data will provide a more accurate assessment of local and national distribution and abundance. This will ultimately help ensure decisions are made on the best available science and evidence. Shooters can help by contributing towards the following initiatives:

a. Bird counts – these enable better understanding of species distribution and population sizes.
b. Bag data submission – this provides a better understanding of harvest and strengthens species population estimates.
c. Marking of birds – ring recovery and reporting enables better understanding of species movement and
survival rates.
d. Disease reporting – enables better understanding of threats to species and potential drivers of population trends.

Conservation

Sustainable shooting is supported by practical conservation action that targets the habitats of quarry and non-quarry species alike. Shooters should, where possible, create management plans to highlight and capture conservation work and their approach to managing harvest. Below are several areas where shooters can take action to support species recovery or maintain species presence during the breeding and/or overwintering season:

a. Undertake targeted habitat creation, restoration and maintenance work.
b. Pest and predator control.
c. Nesting support (for example: fencing, duck nest tubes, provision of maintained islands). 
d. Refuge provision, either for set periods of time (temporal), or over dedicated areas of land (spatial), dependent on site requirements.

Managing disturbance

It is important that shooting does not cause disturbance that impacts on waterbirds to an extent that there is a: 

a. change in local distribution on a continuing basis; and/or
b. change in local abundance on a sustained basis; and/or
c. reduced ability of any significant group of birds to survive, breed, or rear their young.

Disturbance during periods of prolonged cold weather can have significant impacts; shooters must comply with the Joint Nature Conservation Committee (JNCC) and BASC ‘severe weather’ protocols.

Species-specific recommendations

The actions required for each species have been detailed below. 

Common Pochard

Aythya ferina

2023-2028 Recommendation: no take – targeted conservation effort required.

Species trend

The UK hosts a very small number of breeding pochard; however, many over-winter in the UK.

The pochard population shows a ten-year wintering population decline in the UK of greater than 25 per cent between 2008-2018. This decline has been seen on a UK, European and global level and is predicted to continue; as such, the species has been listed as ‘vulnerable’ on the European International Union for Conservation of Nature (IUCN) Red List.

Action to prevent further continued population declines is required across the flyway (north-east to north-west Europe).
Within the UK, it is vital that we better understand the species distribution, abundance, and historic harvest of pochard in order to encourage the small breeding population to thrive. As a result, BASC has provided the following recommendations:

Research required

• Breeding and wintering surveys to better understand local and national distribution and abundance.
• Historic bag returns and the submission of current bag data to better inform harvest estimates (data can be submitted to the Game & Wildlife Conservation Trust (GWCT) National Gamebag Census or BASC Green Shoots Bagged It).

Shooting restrictions

Voluntary moratorium, i.e. shooters should voluntarily refrain from shooting common pochard.

Habitat management

• Maintenance or restoration of freshwater floodplains to provide optimum feeding and roosting environments comprising of deep water (up to 2.5m).
• Maintenance or creation of abundant aquatic plant areas which provide roots, shoots, and seeds for food.
• Targeted predator control in areas where known breeding populations exist.

Stage 2 assessment

Species summary

Pochard show widespread declines across their range, in part a result of declines from an all-time high1. The species originally expanded in size and range due to development of inland fisheries in Eastern Europe which have now been abandoned or intensified, making them less suitable for pochard1.

The highest breeding numbers of pochard are found in Russia and Eastern Europe1. The UK supports a limited percentage of the global breeding population (<1%) and therefore conservation action must be taken at a flyway level to be effective.

Currently, pochard are under the highest AEWA protection and a flyway level action plan is required2. This will likely include increased adoption of non-toxic shot3, wetland restoration and improved understanding of migratory movement and population dynamics1,4.

Reduction in shooting pressure or better monitoring of bag data may contribute to the understanding of hunting pressure and a possible link to the species declining population trend1.

Species conservation status (see Table 1)

The pochard population shows a 10-year wintering population decline in the UK >25% between 2008-20185. Within UK countries, this decline is greatest in Scotland and Wales (-63% in both cases)5. These declines are also highlighted in ‘high’ WeBS Alerts for all UK countries over the long-term (<25 years)6.

Pochard have demonstrated this substantial long and short-term decline at a global7, flyway2, European8 and UK5 level. This trend is predicted to continue. It is suggested that a degree of decline is not only expected but should be accepted to allow the population to return to less artificial levels1. However, this declining trend must stabilise soon to prevent possible species loss1.

Population dynamics

Further research is required to disentangle the drivers of natural mortality and hunting on the pochard population across the flyway1,4,11. Limited studies suggest pochard display high adult survival probabilities, therefore population declines are, in part, thought to be predominantly driven by decreases in juvenile survival and/or poor nesting success11. Adult females do also display poorer survival compared to males, likely a result of increased vulnerability to predation during the breeding season4,11. This may in part be contributing to population trends4, or may in fact be a symptom of poor breeding success11.

 

BoCC9

(2020)

IUCN UK9

(2020)

Europe8

(2021)

EU288

(2021)

AEWA2

(2018)

IUCN Global

(Last updated in 2021)7

CategoryRENVU (W)VU (B)A1bVU
Trend (time period in brackets)

Decreasing5

(2009-2018)

Decreasing (over 3 generations)Decreasing (over 3 generations)

Decreasing

(2009-2018)

Decreasing

Population size estimate Mature

individuals

Breeding: 720 Pairs

Wintering: 29,000 Individuals10

373,000-

679,000

(min-max)

57,000-

110,000

(min-max)

150,000-

150,000

(min-max)

760,000-

790,000

Reason for category

Threatened in Europe and globally.

Severe non-breeding pop decline over 25yrs.

Moderate non-breeding pop decline over longer term.

Moderate breeding range decline over 25 yrs/longer term.

Reduction in the size (either abundance or range) of breeding and non-breeding population.

Declines between 20-

30% over 3 generations.

Population reduction observed.

Population reduction projected.

Population reduction observed.

Population reduction projected.

Species is listed as ‘Threatened’ on IUCN Red List of Threatened Species in most recent BirdLife International report (2021)* All take is prohibited in party range states.

Population reduction observed across majority of range.

Population reduction projected to continue.

WeBS UK 10-year trend (2008/09-2018/19): -39%5 Ÿ BBS UK 10-year trend (2010-2020): n/a**

Table 1. Species conservation status across different scales. *It has been highlighted by BASC that such automatic linkage between IUCN status and levels of protection by AEWA is directly contrary to the IUCN’s advice on the use of its list. **No Breeding Bird Survey data (BBS) due to Pochard primarily being an over-wintering species in the UK.

Hunting and harvest (see Table 2)

The pochard shooting seasons in the UK are not compliant with the Key Concepts of Article 7(4)12. The start date of the open season in England and Wales (1 Sept) overlaps with the estimated end of the reproduction period for pochard in the south of the UK by two ‘decades’ (approx. 20 days). This is therefore in breach of the agreement.

Pochard are not a heavily hunted species in the UK, with low bag numbers reported in recent years (~180 birds in 2012 and ~370 birds in 2016)13. As a result, they are estimated to have low probability of an unsustainable harvest in the UK14. However, this may not be the case on the continent15. A number of BASC registered wildfowling clubs have already adopted a voluntary ban on shooting pochard due to consenting legislative pressure as a result of the species decline, though they recognise this will have no tangible conservation benefit for the local or national pochard population.

Although there are numerous non-hunting pressures facing the species, recent studies3,16 have shown that pochard are one of many species susceptible to lead poisoning, therefore continued and increased use of non-toxic shot is vital for this and other waterbird species. A possible spatial segregation of male and female overwintering locations may also expose female birds (who winter further south in Europe) to increased hunting pressure, thus driving the overall population decline16.

With many wildfowling clubs already undertaking a voluntary moratorium on the shooting of pochard, combined with low bag numbers, the targeted voluntary cessation of shooting is an achievable target. However, this action is not likely to have a significant conservation benefit. As a freshwater duck, inland shooting is likely a greater threat and is out with the jurisdiction of most of the BASC wildfowling club structures. Quarry identification resources are currently being developed within the Wildfowling and Wetland department to help raise awareness and knowledge, particularly among inland wildfowlers.

Species

Species estimated

λmax (95% CI)

Potential excess growth (95% CI)Mean Sustainable Hunt Index (95% CI)Probability of unsustainable harvest
Pochard

1.852

(1.442 – 2.715)

1800

(980 – 3000)

0.359

(0.082 – 0.859)

0.001

Table 2. Estimated sustainability of species harvest in the UK. Table from Ellis & Cameron 2022.

Pressures, action and research

Pressures

Changes in fishery management and the resulting habitat loss in Eastern Europe is the major threat to pochard across their range1,17,18. Climate change is considered a driver of decline in pochard as well as other wildfowl, resulting in reduced ephemeral waterbodies or increased severe weather19. Additionally, changes to water quality due to agricultural activity causing run-off and eutrophication, alongside reduction in wetlands, are major pressures facing this species1,19. Shifts in species composition i.e. increase in carp, foxes and mink and a decrease in black-headed gulls are also suggested to impact pochard populations through competition and predation activity1,19. The combined effect of these pressures is added to by a degree of mortality driven by lead poisoning, an indirect effect of lead ammunition and fishing tackle.3,4,19

Practical action

A flyway-level species action plan is required (NE/NW Europe flyway) in combination with

a UK-level action plan for conservation2. However, coordination is required across the global range due to mixing of populations from different flyways20–22. Improving habitat management in and around commercial fisheries may require incentivisation in eastern European countries1,17. Reducing the impact of development in and around wetland and coastal areas, alongside restoring wetland habitat and improving water quality is vital for this wetland species19. However, water-quality improvement may also make habitat less favourable for pochard23. An increased reduction in lead use (which has been in place since 1999 in certain areas or for certain species, and is currently being phased out across the UK) will be vital to reducing the long-term impact of lead poisoning. In parallel, reduced hunting pressure would lessen the additive effect of the pressures faced by pochard across its range3,19. Isolated action within the UK will have a limited impact due to the proportion of the breeding and wintering population the country supports.

Research action

Improved assessment of bag data demographics is key to understanding drivers of the skewed sex ratio seen in pochard (male-biased due to poor female survival), and any potential role that hunting plays in this shift4. Further understanding of changes in migratory patterns and clarification of major pressures across the flyways are needed to enable an effective action plan to be developed1,4.

References

  1. Fox, D., Caizergues, A., Baik, M. V., Devos, K. & Dvorak, M. Recent changes in the abundance of Common Pochard Aythya ferina breeding in Europe. Wildfowl 66, 22–40 (2016).
  2. Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) – Agreement Text and Annexes As amended by MOP8. (2022).
  3. Newth, L. et al. Poisoning from lead gunshot: Still a threat to wild waterbirds in Britain. Eur J Wildl Res 59, 195–204 (2013).
  4. Brides, , Wood, K. A., Hearn, R. D. & Fijen, T. P. M. Changes in the sex ratio of the Common Pochard Aythya ferina in Europe and North Africa. Wildfowl 67, 100–112 (2017).
  5. Frost, T. M. et al. Waterbirds in the UK 2019/20: The Wetland Bird Survey. (2021).
  6. Woodward, I. D., Frost, T. M., Hammond, M. J. & Austin, G. E. Wetland Bird Survey Alerts 2016/2017: Changes in numbers of wintering waterbirds in the Constituent Countries of the United Kingdom, Special Protection Areas (SPAs), Sites of Special Scientific Interest (SSSIs) and Areas of Special Scientific interest (ASSIs). BTO Research Report 721. bto.org/webs-reporting-alerts (2019).
  7. Birdlife Aythya ferina. The IUCN Red List of Threatened Species 2021: e.T22680358A205288455. https://dx.doi.org/10.2305/IUCN.UK.2021-3.RLTS.T22680358A205288455.en (2021) doi:10.2305/IUCN.UK.2021.
  8. BirdLife European Red List of Birds. https://op.europa.eu/en/publications. (2021) doi:10.2779/967570.
  9. Stanbury, et al. The status of our bird populations: The fifth Birds of Conservation Concern in the United Kingdom, Channel Islands and Isle of Man and second IUCN Red List assessment of extinction risk for Great Britain. British Birds 114, 723–747 (2021).
  10. Woodward, et al. APEP 4: Population estimates of birds in Great Britain and the United Kingdom. British Birds 113, 69–104 (2020).
  11. Folliot, et al. When survival matters: Is decreasing survival underlying the decline of common pochard in western Europe? Wildlife Biol 2020, (2020).
  12. Key concepts of Article 7(4) of Directive 79/409/EEC: Period of reproduction and prenuptial migration of Annex II bird species in the 28 Member States. (2014).
  13. Aebischer, N. J. Fifty-year trends in UK hunting bags of birds and mammals, and calibrated estimation of national bag size, using GWCT’s National Gamebag Eur J Wildl Res 65, (2019).
  14. Ellis, & Cameron, T. An initial assessment of the sustainability of waterbird harvest in the United Kingdom. bioRxiv (2022).
  15. Guillemain, , Aubry, P., Follio, B. & Caizergues, A. Duck hunting bag estimates for the 2013/14 season in France. Wildfowl 66, 126–141 (2016).
  16. Green, E. & Pain, D. J. Possible effects of ingested lead gunshot on populations of ducks wintering in the UK. Ibis 158, 699–710 (2016).
  17. Aghababyan, , Khachatryan, A., Baloyan, S., Ghazaryan, A. & Gevorgyan, V. Assessing the current status of the Common Pochard Aythya ferina in Armenia. Wildfowl 71, 147–166 (2021).
  18. Broyer, & Bourguemestre, F. Common pochard Aythya ferina breeding density and fishpond management in central France. Wildlife Biol 2020, (2020).
  19. Stichting BirdLife Europe, BirdLife International & Article 12 EU population status assessments: Annex B – Bird species’ status and trends report format (Article 12) for the period 2013 – 2018. (2020).
  20. Folliot, , Guillemain, M., Champagnon, J. & Caizergues, A. Patterns of spatial Dstribution and migration phenology of common pochards Aythya ferina in the Western Palearctic: A ring-recoveries analysis. Wildlife Biol 2018, (2018).
  21. Liu, , Keller, I. & Heckel, G. Range-wide genetic population structure of common pochard (aythya ferina): A potentially important vector of highly pathogenic avian influenza viruses. Ecol Evol 1, 529–545 (2011).
  22. Keller, , Korner-Nievergelt, F. & Jenni, L. Within-winter movements: A common phenomenon in the Common Pochard Aythya ferina. J Ornithol 150, 483–494 (2009).
  23. Marsden, S. J. & Bellamy, G. S. Microhabitat characteristics of feeding sites used by diving duck Aythya wintering on the grossly polluted Manchester Ship Canal, Environ Conserv 27, 278–283 (2000).

Northern Pintail

Anas acuta 2023-2028 Recommendation: take a maximum of two birds per day – targeted conservation effort required.

Species trend

The northern pintail population shows a ten-year wintering population decline in the UK of greater than 25 per cent between 2008-2018. This decline is reflected on the European continent within breeding populations in European Russia, Finland and Sweden, and is anticipated to continue. However, due to their large range and relatively high abundance, pintail are not yet considered ‘vulnerable’ to extinction at a global level but are listed as ‘vulnerable’ on the European IUCN Red List. Population trends appear to be driven by pressures at breeding grounds and poor breeding success, as opposed to over-harvesting of adult birds. Due to already low bag numbers in the UK and the limited impact of wintering adult mortality on population demographics, a full moratorium on the species will have limited effect. A moratorium could have a negative impact by disincentivising conservation effort, so continued but controlled harvest is recommended. The UK supports a very small number of breeding individuals; therefore, conservation focus should be on breeding populations abroad and over-wintering pintail populations in the UK. Pintail pair up during the winter and undertake the return migration as a pair, known as a ‘winter pair bond’. Improved understanding of optimal wintering habitat requirements within and outside wetland reserves in the UK, particularly on neighbouring agricultural land, is vital. Based on the species trends and information, BASC has provided the following recommendations.

Research required

  • International flyway-level collaboration with
  • relevant
  • Wintering surveys to better understand local and national distribution and
  • Submission of bag data to better inform harvest estimates (data can be submitted to the GWCT National Gamebag Census or BASC Green Shoots Bagged It).
  • Shooters should support the BASC wing survey to enable better understanding of adult:juvenile and male:female harvest ratios.

Shooting restrictions

  • Two pintail per person, per day, bag limit
  • Should target males where
  • No sale of shot

Habitat management

  • Pintail prefer habitats with low vegetation and shallow water; they will also frequent large inland lakes, ponds, marshes, and coastal lagoons.
  • In order to provide an abundant supply of high-energy and nutritional foods for pintail, wetland water depths should be less than 45cm but preferably less than 15cm for an abundant food source.
  • Weed management can improve habitat for pintail when benefiting native plant

Stage 2 assessment

Species summary

Research on pintail is dominated by North American studies which suggest pintail have failed to respond to an increase in wetlands (often referred to as May ponds in American literature), a habitat type they were previously thought to be influenced by1. In Europe, ephemeral wetlands are still deemed to play an important role in pintail recovery but agricultural foraging areas are equally, if not more important2. The UK supports a very small number of breeding individuals, therefore conservation focus on over-wintering pintail populations will be most beneficial. Improved understanding of optimal wintering habitat requirements within and out-with wetland reserves, particularly on neighbouring agricultural land, is vital. Population trends appear to be driven by pressures at breeding grounds and poor recruitment as opposed to over-harvesting of adult birds3,4.

Species conservation status (see Table 1)

The Northern pintail (hereafter pintail) population shows a 10-year wintering population decline in the UK <25% between 2008-20185. Within the UK countries this trend is mixed, with England and Wales displaying these declines (-27% and -50% respectively) alongside high WeBS alerts for a medium-term (<10 year) decline in Wales6. Conversely, Scotland and N.Ireland are displaying increasing population trends (+36% and + 19% respectively)5. This decline is reflected on the European continent within breeding populations in European Russia, Finland and Sweden, and is anticipated to continue7. However, due to its large range and relatively high abundance, pintail are not yet considered ‘Vulnerable’ to extinction at a global level8.

Population dynamics

Like many other waterbirds, pintail show a male bias in adult birds13. Poor population recovery by pintail in North America is primarily attributed to poor female survival at breeding sites, poor nesting success and low recruitment3,4. Due to already-low bag numbers, and the limited impact of wintering adult mortality on population demographics (including that driven by hunting), removal of this species from Schedule II would have limited impact on the species. Removal of pintail from the quarry list may in fact reduce conservation efforts and data collected about the species.

Hunting and harvest

Pintail shooting seasons in the UK are compliant with the Key Concepts of Article 7(4)14. They are not a heavily hunted species in the UK and bag numbers have decreased over the last 20 years (2004: 1,400, 2012: 800, 2016: 680)15. As a result, they are estimated to have low probability of an unsustainable harvest in the UK16. Within Europe, there is limited data on pintail bag numbers but France and Scandinavian countries have the largest documented bags17. In North America, where the majority of pintail studies have been undertaken, restricted hunting bags and days have not resulted in pintail population recovery. It is suggested that hunting is not a major driver of pintail population declines (or lack of recovery)3,4,18,19. However, anthropogenic disturbance, caused in part by hunting, is suggested to influence the spatial distribution and energetic costs of overwintering birds20–22. It is also possible that there is a bias in the hunting of male pintail due to their easily-identifiable appearance13. Additionally, pintail are susceptible to lead poisoning, with increased risk of lead shot ingestion in agricultural areas due to their dependence on farmland for night-time foraging23,24. In these environments, lead shot is still used, however we may see a reduction in poisoning incidence with the phasing out of lead shot in the UK.
BoCC9 (2020) IUCN UK9 (2020) Europe7 (2021) EU287 (2021) AEWA10 (2018) IUCN Global8 (Last updated in 2019)
Category A CR VU (B) EN (B) B1 LC
Trend (time period in brackets) Decreasing5 (2008-2018) Decreasing (over 3 generations) Decreasing (over 3 generations) Stable/ Increasing (2009-2018) Decreasing
Population size estimate Mature individuals Breeding: 27 Pairs Wintering: 20,000 Individuals11 310,000- 401,000 (min-max) 9,100-37,600 (min-max) 74,000- 74,000 (min-max) 4,700,000- 4,800,000
Reason for category Threatened in Europe. Moderate breeding pop. decline over 25yrs. Moderate breeding range decline over 25yrs or longer term. Breeding Rarity. Non-breeding population show localisation and are of international importance. Small breeding population size and continuing decline by >10% over 3 generations. Reduction in the size of non-breeding pop. (either abundance or range) over 3 generations, with declines of at least 20%, but less than 30% over 3 generation lengths. Population reduction observed, estimated, inferred, or suspected in the past where the causes of reduction may not have ceased OR may not be understood OR may not be reversible. Population reduction projected, inferred or suspected to be met in the future (up to a maximum of 100 years). An observed, estimated, inferred, projected or suspected population reduction where the time period must include both the past and the future (up to a max. of 100 years in future), and where the causes of reduction may not have ceased OR may not be understood OR may not be reversible. Populations numbering between 25,000 and around 100,000 individuals and but do not fulfil the conditions of: a)  concentrated distribution, b)  severe habitat decline, c)  long term decline, d)  large population fluctuations, e)  rapid short-term decline or f)  data deficient. Due to a large range and large population size, combined with a <30% decline over 3 generations, the population does not approach thresholds for ‘Vulnerable’.
WeBS UK 10-year trend (2008/09-2018/19): -22%5 ● BBS UK 10-year trend (2010-2020): n/a**
Table 1. Species conservation status across different scales. *It has been highlighted by BASC that such automatic linkage between IUCN status and levels of protection by AEWA is directly contrary to the IUCN’s advice on the use of its list. **No Breeding Bird Survey data (BBS) due to Northern pintail primarily being an over-wintering species and very rare breeder in the UK12.

Pressures, action and research

Pressures Habitat loss, driven by both climate change (increased drought) and anthropogenic factors (abstraction and agricultural intensification) are considered major drivers of pintail decline and the populations current failure to recover1,19,21,25,26. Lead poisoning from hunting and fishing activity is also highlighted as a pressure facing pintail and many other migratory waterbirds in the UK24,26. Additionally, avian influenza is considered a threat to (and exacerbated by) pintail due to their long-distance, intercontinental movements and mixing with other wildfowl27,28. However, the long-term population level impacts of this are unknown. Practical action Within the UK, provision of high-quality over-wintering habitat is likely to have the greatest positive impact on pintail populations. Such wintering habitat comprises wetland and marshland areas in close proximity to seed-rich agricultural land, particularly areas that support ephemeral wetland1,2,19,21,29. The provision of refuge areas (wetlands and ponds) close to agricultural foraging sites are important for pintail in areas where hunting and other anthropogenic disturbance occurs, particularly in periods of prolonged cold weather20–22,26. Continued suspension of shooting during cold periods will therefore also reduce disturbance and energy demands on over-wintering birds22,26. Ongoing phasing out of lead-shot is vital, not only in wetland areas but on agricultural land utilised by pintail for foraging23,24,26. Due to the small breeding population, efforts to support their persistence will of course be beneficial, but the overall population impact will be negligible. If female mortality is a driver of population decline, enhanced predator management and reduced disturbance at nesting sites is recommended1,26. Research action Greater understanding of juvenile recruitment is vital across the species range, to better guide conservation efforts for over-wintering and breeding birds3. This primarily requires effort at breeding grounds, but first-year juvenile ringing and monitoring will provide insight into survival between natal sites, on migratory routes and at wintering grounds. Clearer understanding of optimal over-wintering habitat required for pintail (both within and outside of wetlands) in the UK will help guide recommendations for agricultural activity and land-management in important wildfowl areas20.

References

  1. HMiller, R. & Duncan, D. C. The Northern Pintail in North America: Status and Conservation Needs of a Struggling Population. Bulletin 27, 788–800 (1973).
  2. Parejo, et al. Day and night use of habitats by northern pintails during winter in a primary rice-growing region of Iberia. PLoS One 14, (2019).
  3. Rice, M. B., Haukos, D. A., Dubovsky, J. A. & Runge, M. C. Continental survival and recovery rates of Northern pintails using band-recovery Journal of Wildlife Management 74, 778–787 (2010).
  4. Bartzen, B. A. & Dufour, K. W. Northern Pintail (Anas acuta) survival, recovery, and harvest rates derived from 55 years of banding in Prairie Canada, 1960–2014. Avian Conservation and Ecology 12, (2017).
  5. Frost, T. M. et al. Waterbirds in the UK 2019/20: The Wetland Bird Survey. (2021).
  6. Woodward, I. D., Frost, T. M., Hammond, M. J. & Austin, G. E. Wetland Bird Survey Alerts 2016/2017: Changes in Numbers of Wintering Waterbirds in the Constituent Countries of the United Kingdom, Special Protection Areas (SPAs), Sites of Special Scientific Interest (SSSIs) and Areas of Special Scientific Interest (ASSIs). BTO Research Report 721. bto.org/webs-reporting-alerts (2019).
  7. BirdLife European Red List of Birds. https://op.europa.eu/en/publications. (2021) doi:10.2779/967570.
  8. Anas The IUCN Red List of Threatened Species 2019: E.T22680301A153882797. https://dx.doi.org/10.2305/IUCN.UK.2019-3.RLTS.T22680301A153882797.en (2019) doi:10.2305/IUCN.UK.2019.
  9. Stanbury, et al. The status of our bird populations: the fifth Birds of Conservation Concern in the United Kingdom, Channel Islands and Isle of Man and second IUCN Red List assessment of extinction risk for Great Britain. British Birds 114, 723–747 (2021).
  10. Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) – Agreement Text and Annexes As Amended by MOP8. (2022).
  11. Woodward, et al. APEP 4: Population estimates of birds in Great Britain and the United Kingdom. British Birds 113, 69–104 (2020).
  12. Eaton, M. Rare breeding birds in the UK in 2019. British Birds 114, 646–704 (2021).
  13. Wood, A., Brides, K., Durham, M. E. & Hearn, R. D. Adults have more male-biased sex ratios than first-winter juveniles in wintering duck populations. Avian Res 12, (2021).
  14. Key Concepts of Article 7(4) of Directive 79/409/EEC: Period of Reproduction and Prenuptial Migration of Annex II Bird Species in the 28 Member States. (2014).
  15. Aebischer, N. J. Fifty-year trends in UK hunting bags of birds and mammals, and calibrated estimation of national bag size, using GWCT’s National Gamebag Eur J Wildl Res 65, (2019).
  16. Ellis, B. & Cameron, T. C. An initial assessment of the sustainability of waterbird harvest in the United Kingdom. Journal of Applied Ecology 59, 2839–2848 (2022).
  17. Guillemain, , Aubry, P., Follio, B. & Caizergues, A. Duck hunting bag estimates for the 2013/14 season in France. Wildfowl 66, 126–141 (2016).
  18. Sedinger, S. & Herzog, M. P. Harvest and dynamics of duck populations. Journal of Wildlife Management vol. 76 1108–1116 Preprint at https://doi.org/10.1002/jwmg.370 (2012).
  19. Migoya, , Baldassarre, G. & Losito, M. Diurnal activity budgets and habitat functions of Northern Pintail Anas acuta wintering in Sinaloa, Mexico. Wildfowl 45, 134–146 (1994).
  20. Casazza, L., Coates, P. S., Miller, M. R., Overton, C. T. & Yparraguirre, D. R. Hunting influences the diel patterns in habitat selection by northern pintails Anas acuta. Wildlife Biol 18, 1–13 (2012).
  21. Cox, R. & Afton, A. D. Use of Habitats by Female Northern Pintails Wintering in Southwestern Louisiana. J Wildl Manage 61, 435–443 (1997).
  22. Taylor, P. et al. Influence of Environmental Stress and Anthropogenic Disturbance Influence of Environmental Stress and Anthropogenic Disturbance on the Energy Expenditure of Wintering Northern Pintails (Anas on the Energy Expenditure of Wintering Northern Pintails (Anas acuta) acuta). Waterbirds 42, 294–303 (2019).
  23. Mateo, R., Martlnez-Vilalta, A. & Guitart, R. Lead shot pellets in the Ebro delta, Spain: Densities in sediments and prevalence of exposure in Environmental Pollution 96, 335–341 (1997).
  24. Newth, L. et al. Poisoning from lead gunshot: Still a threat to wild waterbirds in Britain. Eur J Wildl Res 59, 195–204 (2013).
  25. Podruzny, M., Devries, J. H. & Armstrong, L. M. Long-term response of Northern pintails to changes in wetlands and agriculture in the Canadian Prairie Pothole Region. J Wildl Manage 66, 993–1010 (2002).
  26. Stichting BirdLife Europe, BirdLife International & Article 12 EU Population Status Assessments: Annex B – Bird Species’ Status and Trends Report Format (Article 12) for the Period 2013 – 2018. (2020).
  27. Jahangir, et al. Surveillance of Avian Influenza Viruses in Northern Pintails (Anas acuta) in Tohoku District, Japan. Avian Dis 52, 49–53 (2008).
  28. Koehler, v., Pearce, J. M., Flint, P. L., Franson, J. C. & Ip, H. S. Genetic evidence of intercontinental movement of avian influenza in a migratory bird: The northern pintail (Anas acuta). Mol Ecol 17, 4754–4762 (2008).
  29. Cox, R. & Afton, A. D. Evening flights of female Northern Pintails from a major roost site. Condor 98, 810–819 (1996).
  30. Balmer, E. et al. Bird Atlas 2007-11: The Breeding and Wintering Birds of Britain and Ireland. (Thetford: BTO, 2013).

Goldeneye

Bucephala clangula 2023-2028 Recommendation: delay shooting until October where resident breeding goldeneye are present.

Species trend

Goldeneye show a ten-year wintering population decline in the UK of greater than 25 per cent. Declines in the UK appear to be driven primarily by climate change and are a result of a redistribution of the species across the European flyway to more north-eastern edges of their range. At a global level the population appears stable and therefore of ‘least concern’. Enhancement of breeding habitat in the UK will have only a limited impact, as goldeneye are rare breeders. Taking these trends into consideration, BASC has provided the following recommendations:

Research required

  • Breeding and wintering surveys to better understand local and national distribution and abundance.
  • Submission of bag data to better inform harvest estimates (data can be submitted to GWCT National Gamebag Census or BASC Green Shoots Bagged It).
  • Shooters should support the BASC wing survey to enable better understanding of adult:juvenile and male:female harvest ratios.
  • Increased ringing, ring resighting and ring recovery reporting

Shooting restrictions

  • Should delay shooting until October where resident breeding goldeneye are
  • Show restraint, even when resident birds are Shoot what you need, not what you can.

Habitat management

  • The installation of nest boxes has been shown to support goldeneye nesting and increase brood numbers where natural tree cavities are limited.
  • Pest and predator

Stage 2 assessment

Species summary

Goldeneye declines in the UK appear to be driven primarily by climate change6–9. Enhancement of breeding habitat in the UK will have limited impact as goldeneye are rare breeders10, however continued monitoring of wintering bird numbers, bag data and hunting bag demographics, for example through the Wing Survey, is recommended. This data will contribute to our understanding of range shifts and recruitment of goldeneye across the flyway.

Species conservation status (see Table 1)

Goldeneye shows a 10-year wintering population decline in the UK of >25% between 2008-20181. Within UK countries, the severity of decline is varied, with Northern Ireland showing the most significant decline (-71%) alongside high WeBS alerts for long- (<25 years), medium-(<10 years) and short-term (<5 years)2. These declines are reflected but less severe in England and Wales (-22% and -18% respectively). Scotland however, displays marginal increases (+4%)1. This decline is also seen on the European continent within breeding populations, however the severity of the decline does not push the species into the ‘Vulnerable’ category3. At a flyway level, this decline has also been identified and action is recommended to prevent a continued downward trajectory4. At a global level however, the population appears stable and therefore of ‘Least Concern’5.
BoCC11 (2020) IUCN UK11 (2020) Europe3 (2021) EU283 (2021) AEWA4 (2018) IUCN Global (Last updated in 2018)5
Category R VU LC (B) LC (B) B2c LC
Trend (time period in brackets) Decreasing (2008/09-2018/19) Decreasing (over 3 generations) Decreasing (over 3 generations) Decreasing (2009-2018) Stable
Population size estimate Mature individuals Breeding: 200 Males Wintering: 21,000 Individuals12 770,000- 990,000 (min-max) 374,000- 481,000 (min-max) 750,000- 1,500,000 (min-max) 2,700,000- 4,700,000
Reason for category Severe non-breeding pop decline over 25yrs. Breeding Rarity V small breeding pop/ restricted distribution with less than 15,000 individuals Non-breeding pop: Reduction in the size (either abundance or range) of non-breeding pop. measured over 3 generations. Declines of 20- 30% over 3 generations. n/a n/a Population >100,000 individual but considered to be in need of special attention due to long-term decline Large range and population size. Stable population trend.

WeBS UK 10-year trend (2008/09-2018/19): -26%1 ● BBS UK 10-year trend (2010-2020): n/a**

Table 1. Species conservation status across different scales. *It has been highlighted by BASC that such automatic linkage between IUCN status and levels of protection by AEWA is directly contrary to the IUCN’s advice on the use of its list. **No Breeding Bird Survey data (BBS) due to goldeneye primarily being an over-wintering species in the UK and a rare breeding bird10.

Population dynamics

Goldeneye declines in the UK appear to be driven primarily by climate change6–9. The species has shown north-easterly distributional shifts in abundance since the 1980’s, with increasing population trends in Finland and Sweden8. This shift may result in elevated pressures on more northern populations in Scandinavia (as a result of hunting and unprotected sites). The species therefore requires a flyway-level action plan4,6,8.

Hunting and harvest (see Table 2)

Goldeneye shooting seasons in the UK are compliant with the Key Concepts of Article 7(4)13. They are not a heavily hunted species in the UK and bag numbers have remained low over the last 20 years (2004: 680, 2012: 200, 2016: 450)14. As a result, they are estimated to have low probability of an unsustainable harvest in the UK15. Within Europe, Scandinavian countries have the largest harvest of goldeneye16. However, even within these countries, hunting is not thought to be a major driver of population declines seen in goldeneye17,18. Indirect effects such as lead poisoning are also not prevalent in the species5,17. However, abundance shifts across the flyway to more north-eastern edges of the range due to climate change may lead to unsustainable harvest levels on these more northern populations8,17,18. Shifts in migration and breeding dates may have a knock-on impact on UK shooting seasons in the future.
Species Species estimated λmax (95% CI) Potential excess growth (95% CI) Mean Sustainable Hunt Index (95% CI) Probability of unsustainable harvest
Goldeneye 1.713 (1.449 – 2.450) 5,600 (3700 – 9500) 0.201 (0.026 – 0.474) 0.000
Table 2. Estimated sustainability of species harvest in the UK. Table from Ellis & Cameron 2022.

Pressures, action and research

Pressures Climatic changes over the last 30 years have resulted in shifts in migratory and breeding timing in goldeneye, alongside a redistribution of the species across the European flyway to more north-eastern edges of their range6–9. These changes expose goldeneye to new, potentially unprotected migration and stopover sites, possible changes in hunting pressure and overall alteration to waterbird assemblages6,8. Improvement of water quality and sewage treatment may have driven declines in goldeneye in previously contaminated but productive waterbodies5,19. In parallel, increases in invertebrate-eating fish and introduction of fish into previously fish-free lakes has driven resource competition between goldeneye and fish20,21. Out with the UK, changes to forestry management in breeding grounds have also potentially reduced nest site availability22. Practical action Goldeneye regularly utilise large secondary tree cavities for nesting. With increased intensification of forestry and reduced availability of cavities and deadwood, goldeneye breeding success may be limited22. The installation of nest boxes has shown to support goldeneye nesting and increase brood numbers where natural cavities are limited5,22–25. However, this will have a limited impact in the UK where goldeneye is a rare breeding bird10. Reduction of disturbance and limiting urbanisation around key sites for goldeneye9 will likely benefit overwintering birds in the UK9,26. These sites will be more productive for goldeneye and other invertebrate-feeding ducks if fish populations are limited20,21. Research action Further understanding of the density-dependent population dynamics will enhance understanding of population trends and density-limiting factors27,28. Much of this research must be undertaken at breeding as opposed to wintering grounds. With population shifts to a more north-eastern distribution, monitoring of reproductive success, recruitment and harvest rates must continue to ensure a sustainable take of goldeneye at both country and flyway levels6–9.

References

  1. Frost, T. M. et al. Waterbirds in the UK 2019/20: The Wetland Bird Survey. (2021).
  2. Woodward, I. D., Frost, T. M., Hammond, M. J. & Austin, G. E. Wetland Bird Survey Alerts 2016/2017: Changes in numbers of wintering waterbirds in the Constituent Countries of the United Kingdom, Special Protection Areas (SPAs), Sites of Special Scientific Interest (SSSIs) and Areas of Special Scientific interest (ASSIs). BTO Research Report 721. bto.org/webs-reporting-alerts (2019).
  3. BirdLife European Red List of Birds. https://op.europa.eu/en/publications. (2021) doi:10.2779/967570.
  4. Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) – Agreement Text and Annexes As amended by MOP8. (2022).
  5. BirdLife Bucephala clangula. The IUCN Red List of Threatened Species 2018. https://dx.doi.org/10.2305/IUCN.UK.2018- 2.RLTS.T22680455A132529366.en (2018) doi:10.2305/IUCN.UK.2018.
  6. Lehikoinen, & Jaatinen, K. Delayed autumn migration in northern European waterfowl. J Ornithol 153, 563–570 (2012).
  7. Clark, G., Pöysä, H., Runko, P. & Paasivaara, A. Spring phenology and timing of breeding in short-distance migrant birds: Phenotypic responses and offspring recruitment patterns in common goldeneyes. J Avian Biol 45, 457–465 (2014).
  8. Lehikoinen, et al. Rapid climate driven shifts in wintering distributions of three common waterbird species. Glob Chang Biol 19, 2071–2081 (2013).
  9. Stichting BirdLife Europe, BirdLife International & Article 12 EU population status assessments: Annex B – Bird species’ status and trends report format (Article 12) for the period 2013 – 2018. (2020).
  10. Eaton, M. Rare breeding birds in the UK in 2019. British Birds 114, 646–704 (2021).
  11. Stanbury, et al. The status of our bird populations: the fifth Birds of Conservation Concern in the United Kingdom, Channel Islands and Isle of Man and second IUCN Red List assessment of extinction risk for Great Britain. British Birds 114, 723–747 (2021).
  12. Woodward, et al. APEP 4: Population estimates of birds in Great Britain and the United Kingdom. British Birds 113, 69–104 (2020).
  13. Key concepts of Article 7(4) of Directive 79/409/EEC: Period of reproduction and prenuptial migration of Annex II bird species in the 28 Member States. (2014).
  14. Aebischer, N. J. Fifty-year trends in UK hunting bags of birds and mammals, and calibrated estimation of national bag size, using GWCT’s National Gamebag Eur J Wildl Res 65, (2019).
  15. Ellis, & Cameron, T. An initial assessment of the sustainability of waterbird harvest in the United Kingdom. bioRxiv (2022).
  16. Guillemain, , Aubry, P., Follio, B. & Caizergues, A. Duck hunting bag estimates for the 2013/14 season in France. Wildfowl 66, 126–141 (2016).
  17. Pöysä, H., Rintala, J., Lehikoinen, A. & Väisänen, R. A. The importance of hunting pressure, habitat preference and life history for population trends of breeding waterbirds in Eur J Wildl Res 59, 245–256 (2013).
  18. Holopainen, et al. Associations between duck harvest, hunting wing ratios and measures of reproductive output in Northern Europe. Eur J Wildl Res 64, (2018).
  19. Campbell, H. The Impact of Changes in Sewage Treatment on Seaducks Wintering in the Firth of Forth, Scotland. Biol Conserv 28, 173–180 (1984).
  20. Eriksson, O. G. Competition Between Freshwater Fish and Goldeneyes Bucephala clangula (L.) for Common Prey. Oecologia (Berl.) 41, 99–107 (1979).
  21. Nummi, P., Väänänen, V. M., Rask, M., Nyberg, K. & Taskinen, K. Competitive effects of fish in structurally simple habitats: Perch, invertebrates, and goldeneye in small boreal Aquat Sci 74, 343–350 (2012).
  22. Corrigan, M., Scrimgeour, G. J. & Paszkowsk, C. Nest Boxes Facilitate Local-Scale Conservation of Common Goldeneye (Bucephala clangula) and Bufflehead (Bucephala albeola) in Alberta, Canada. Avian Conservation and Ecology 6, (2011).
  23. Sénéchal, , Gauthier, G. & Savard, J.-P. L. Nesting Ecology of Common Goldeneyes and Hooded Mergansers in a Boreal River System. Wilson J Ornithol 120, 732–742 (2008).
  24. Savard, -P. L. & Robert, M. Use of Nest Boxes by Goldeneyes in Eastern North America. Source: The Wilson Journal of Ornithology vol. 119 https://www.jstor.org/stable/20455945?seq=1&cid=pdf-(2007).
  25. Dow, & Fredga, S. Selection of nest sites by a hole-nesting duck, the Goldeneye Bucephala clangula. Ibis 127, 16–30 (1985).
  26. Musilová, , Musil, P., Zouhar, J. & Adam, M. Changes in habitat suitability influence non-breeding distribution of waterbirds in central Europe. Ibis 160, 582–596 (2018).
  27. Lawson, A. J., Sedinger, J. S. & Taylor, E. J. Identifying demographic and environmental drivers of recruitment and population growth in a cavity-nesting sea duck J Avian Biol 48, 1394–1405 (2017).
  28. Zicus, M. C. & Henives, S. K. Nest prospecting by common goldeneyes. Condor 91, 807–812 (1989).

Greater Scaup

Aythya marila

Northern Ireland only

2023-2028 Recommendation: show restraint, targeted research and conservation effort required.

Species trend

The UK does not host a breeding population of scaup, with only one or two pairs recorded each year; however, many overwinter in the UK.

The scaup population shows a ten-year wintering population decline in the UK of greater than 25 per cent between 2008-2018. This decline has been seen on a UK level but not replicated at a European or global level, where it is listed as of ‘least concern’.
The decline in the UK overwintering population correlates with changes in climate, food supply and other pressures. The eastern European population now winters closer to their breeding grounds, a phenomenon known as short-stopping.

With sufficient protected areas and effective habitat management, shooting restrictions are not necessary. However, it is vital that monitoring of abundance, productivity and bag data is enhanced to maximise the conservation benefits of future actions.
Based on the species trends and information available, BASC has provided the following recommendations:

Research required

  • Wintering surveys to better understand local and national distribution and
  • Submission of bag data is required to better inform harvest estimates (data can be submitted to GWCT National Gamebag Census or BASC Green Shoots Bagged It).
  • Shooters should support the BASC wing survey to enable better understanding of adult:juvenile and male:female harvest ratios.
  • Increased ringing, ring resighting, and ring recovery reporting

Shooting restrictions

  • Should show
  • Site-based considerations

Habitat management

  • Maintenance or restoration of large water habitats, either coastal or freshwater, to provide optimum feeding and roosting environments comprising of deep water (1m to 5m).
  • Minimise impacts on the sea bed/lake bed to ensure availability of suitable

Stage 2 assessment

Species summary

Greater scaup (herein scaup), is a migratory diving duck found across large parts of the Northern Hemisphere. The north-eastern flyway population overwinter in the UK from Iceland, and historically Russia and Fennoscandia, rarely breeding in the UK1–3. Previously high population sizes in the mid-late 1900’s have declined substantially, resulting in an unfavourable conservation status across Europe1,4–6. In the UK, this decline in wintering population size has been driven predominantly by short-stopping of birds from Russia and Fennoscandia7.

In both North America and Europe, drivers of decline in the species remain unclear and may be linked to climate, predation, density or a combination of these factors7–9. The majority of scaup-focussed evidence is based on North American populations and identifies a decline in female survival and recruitment10,11, however drivers are somewhat unclear and these studies must be interpreted with caution. Research within flyway-relevant populations identifies bycatch from fisheries as the main human-mediated driver of mortality.

Species conservation status (see Table 1)

Scaup show a 54% decline overall in the UK over the last 10 years (2010/11-2020/21)6. This is driven by declines in wintering populations in N Ireland (-76%), England (-36%) and Scotland (-29%) during this time period. However, the Welsh population appears to be increasing (+24%) after a 25-year decline of -93%. These declines are shared across the continent of Europe5. However, the North-western flyway population appears to be increasing and remains a substantial size2. The global population remains large but is showing a decline thought to be driven by changes in human activity and climate change3.

 

BoCC12

(2020)

IUCN UK12

(2020)

Europe5

(2021)

EU285

(2021)

AEWA13

(2018)

IUCN Global (Last updated in 2018)
CategoryRENLCENC1LC
Trend (time period in brackets)

Decreasing6

(2010/11-2020/21)

Decreasing (over 3 generations)Decreasing (over 3 generations)

Increasing

(2009-2018)

Decreasing (over 3 generations)
Population size estimate Mature individuals

Breeding: n/a

Wintering: 6,400 Individuals14

96,400-

170,000

(min-max)

 

2,100-3,000

(min-max)

240,000-

280,000

(min-max)

 

4,920,000-

5,130,000

Reason for categorySevere non-breeding pop decline over longer term; Moderate non-breeding pop decline over 25yrs; non-breeding localisationReduction in the size (either abundance or range) of the
non-breeding pop of 20-30% over 3 generations
n/aPopulation reduction of >50% in 3 generations. Causes of
reduction may not be understood or have ceased. Population fewer than 2,500 mature individuals showing decline of >20% in 3 generations.
Pop. numbering over ~100,000 individuals that could significantly benefit from international cooperation but
do not show rapid or long-term declines, range contractions,
major habitat threats or are data deficient.
n/a
WeBS UK 10-year trend (2008/09-2018/19): -54%15 ● BBS UK 10-year trend (2010-2020): n/a**

Table 1. Species conservation status across different scales. *It has been highlighted by BASC that such automatic linkage between IUCN status and levels of protection by AEWA is directly contrary to the IUCN’s advice on the use of its list. **No Breeding Bird Survey data (BBS) due to Scaup primarily being an over-wintering species in the UK.

Population dynamics

The European population is demonstrating a north-eastern shift, likely driven by climate change and the appearance of more appropriate wintering habitat nearer to breeding grounds7. As a result, parts of the Baltic Sea are now key overwintering sites7,16. The overwintering populations of scaup in the UK, Ireland and the Netherlands have declined in the last 30 years due to this short-stopping, particularly by the Russian and Fennoscandian populations7. The UK and Ireland now predominantly host the over-wintering Icelandic population, therefore the mixing of Russian and Icelandic birds may become even more reduced with time, creating distinct geographic populations7. This shift, combined with inadequate conservation measures in new overwintering sites in central Europe, is posing a significant threat to the population at large7. Scaup, like many other waterbirds, demonstrate an uneven sex ratio with a male bias17. Population compositions in Northern Ireland also suggest differential migration, with females often migrating further south to winter18.

Scaup often form mixed flocks with tufted duck A. fuligula and pochard A.ferina during migration and wintering19. BTO ringing data suggests the species is relatively short-lived (typically live three years, breeding in year two), with an adult survival of less than 50% therefore it is likely that reproductive output (as opposed to adult survival) plays an important role in population dynamics.

Hunting and harvest

Scaup shooting seasons in Northern Ireland are compliant with the Key Concepts of Article 7(4)20. There are no current or historical bag number estimates published for scaup.

Therefore, it is difficult to determine the level of hunting pressure or estimate a Sustainable Harvest Index (SHI) which has been done for more common waterbird quarry21. Scaup can only be hunted in ten EU Member States3. Limited research suggests harvest has a negligible impact on the population as a whole3,10. Like many other waterbirds, scaup are susceptible lead shot ingestion, therefore the continued use of non-toxic shot will benefit the species22. North American studies find little evidence that harvest pressure is driving declines in greater and lesser scaup, however lower female survival and poor recruitment are contributing factors9–11. It is important to note that these studies focus on North American populations and the same processes may not be in play within the European flyways.

Pressures, action and research

Pressures

Scaup predominantly feed at night in shallow coastal or brackish water but will winter inland near to the coast1,7,19. These areas are subject to commercial and recreational activities and by-catch by commercial fisheries is a limiting factor for many diving duck populations in Europe3,7,16,23. Other fishing activity such as dredging impacts scaup food resource availability in key sites7. Due to a predominantly shellfish-centric diet, the species is also vulnerable to changes in water quality24. Distribution of wintering birds has also shown to be correlated with food availability and distribution4. Historically, scaup numbers were boosted by cockle harvesting in Scotland, but declined following its cessation4. In parts of their European distribution, scaup depend on zebra mussels (a non-native) for food. There is therefore a trade off between invasive species eradication and supporting wintering waterfowl19. As with other diving ducks, feeding near water treatment discharge was common and more recent improvements in water quality may have contributed to population declines1. Scaup are also susceptible to avian influenza and due to large inter-continental movements may play a role in the spread of the disease25. The impact of climate change on both breeding and overwintering habitat are suggested to impact survival and productivity of scaup due to varying weather conditions (i.e. snow cover) and food availability3,7,9. As a late-nesting species, the reduced flexibility of scaup to adjust their timing of breeding makes them more susceptible to such changes26.

Practical action

Preservation and protection of breeding grounds and key wintering grounds in northern Europe are key3,27. Since scaup also display and form pair bonds at wintering sites, adequate food resources are important for the population at these non-breeding sites prior to return migration19. Limiting fishing operations in areas with high overwintering diving duck numbers would reduce bycatch and entanglement16,23. Up-to-date species management plans are required for SPA’s where the species occurs7. Scaup are bottom-feeding divers therefore reducing disturbance to the floor of waterbodies (especially 1-5m in depth) encourages the retention of prey such as bivalves or chironomid larvae19.

Research action

An increase in bag data from the UK will enable a greater understanding of the Icelandic flyway population composition. This may allow for drivers of scaup declines to be better understood. Increased tagging and ringing research may provide further data on short-stopping behaviour and potential segregation of Icelandic and Russian/Fennoscandian birds1.

References

  1. Kirby, S., Evans, R. J. & Fox, A. D. Wintering seaducks in Britian and Ireland: populations, threats, conservation and research priorities. Aquat Conserv 3, 105–137 (1993).
  2. Wetlands International. Waterbird Populations Portal. wpp.wetlands.org (2022).
  3. BirdLife International. Aythya Marila. The IUCN Red List of Threatened Species 2018 e.T22680398A132525108. http://dx.doi.org/10.2305/IUCN.UK.2018- (2018) doi:10.2305/IUCN.UK.2018.
  4. Quinn, L., Still, L., Carrier, M. C., Kirby, J. S. & Lambdon, P. Scaup Aythya marila numbers and the Cockle Cardium edule fishery on the Solway Firth: are they related? Wildfowl 47, 187–194 (1996).
  5. BirdLife European Red List of Birds. https://op.europa.eu/en/publications. (2021) doi:10.2779/967570.
  6. Austin, E. et al. Waterbirds in the UK 2021/22: The Wetland Bird Survey and Goose & Swan Monitoring Programme. . (2023).
  7. Marchowski, et al. Effectiveness of the European Natura 2000 network to sustain a specialist wintering waterbird population in the face of climate change. Sci Rep 10, (2020).
  8. Ross, B. & Devink, J.-M. Combined effects of climate, predation, and density dependence on Greater and Lesser Scaup population Ecological Applications 25, 1606–1617 (2015).
  9. Tatman, M. et al. Tatman et al 2009 – nest success and duckling survival of greater scaup in New Brunswick. The Canadian Field Naturalist 123, 323–328 (2009).
  10. Afton, D. & Anderson, M. G. Declining Scaup Populations: A Retrospective Analysis of Long-Term Population and Harvest Survey Data. J Wildl Manage 65, 781–796 (2001).
  11. Austin, E. et al. Declining Scaup Populations: Issues, Hypotheses, and Research Needs. Wildl Soc Bull 28, 254–263 (2000).
  12. Stanbury, et al. The status of our bird populations: the fifth Birds of Conservation Concern in the United Kingdom, Channel Islands and Isle of Man and second IUCN Red List assessment of extinction risk for Great Britain. British Birds 114, 723–747 (2021).
  13. Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) – Agreement Text and Annexes As Amended by MOP8. (2022).
  14. Woodward, et al. APEP 4: Population estimates of birds in Great Britain and the United Kingdom. British Birds 113, 69–104 (2020).
  15. Frost, T. M. et al. Waterbirds in the UK 2019/20: The Wetland Bird Survey. (2021).
  16. Marchowski, & Leitner, M. Conservation implications of extraordinary Greater Scaup (Aythya marila) concentrations in the Odra Estuary, Poland. Condor 121, (2019).
  17. Sotherland, P. R. & Rahn, H. On the composition of bird eggs. Condor 89, 48–65 (1987).
  18. Evans, M. & Day, K. R. Migration patterns and sex ratios of diving ducks wintering in Northern Ireland with specific reference to Lough Neagh. Ringing and Migration 20, 358–363 (2001).
  19. Marchowski, et al. The importance of non-native prey, the zebra mussel Dreissena polymorpha, for the declining greater scaup Aythya marila: A case study at a key European staging and wintering site. PLoS One 10, (2015).
  20. Key Concepts of Article 7(4) of Directive 79/409/EEC: Period of Reproduction and Prenuptial Migration of Annex II Bird Species in the 28 Member States. (2014).
  21. Ellis, B. & Cameron, T. C. An initial assessment of the sustainability of waterbird harvest in the United Kingdom. Journal of Applied Ecology 59, 2839–2848 (2022).
  22. Demendi, & Petrie, S. A. Shot Ingestion in Scaup on the Lower Great Lakes After Nontoxic Shot Regulations in Canada. Wildl Soc Bull 34, 1101–1106 (2006).
  23. Marchowski, D., Jankowiak, Ł., Ławicki, Ł., Wysocki, D. & Chylarecki, P. Fishery bycatch is among the most important threats to the European population of Greater Scaup Aythya Bird Conserv Int 30, 176–193 (2020).
  24. Cervencl, & Alvarez Fernandez, S. Winter distribution of Greater Scaup Aythya marila in relation to available food resources. J Sea Res 73, 41–48 (2012).
  25. Spaulding, F., Mclaughlin, J. F., Glenn, T. C. & Winker, K. Estimating movement rates between Eurasian and North American birds that are vectors of avian Avian Dis 66, 155–164 (2022).
  26. Drever, C. et al. Population vulnerability to climate change linked to timing of breeding in boreal ducks. Glob Chang Biol 18, 480–492 (2012).
  27. Fox, D. et al. Current and Potential Threats to Nordic Duck Populations — a Horizon Scanning Exercise. Annales Zoologici Fennici vol. 52 (2015).

European White-fronted Goose

Anser albifrons England and Wales only 2023-2028 Recommendation: take a maximum of two birds, per person, per day – targeted research required.

Species trend

The European white-fronted goose population shows a moderate decline in the UK in the medium term and a significant decline of greater than 50 per cent in the long term. However, this decline is not reflected on the European continent where the large population remains stable or increasing. This is reflected in the European IUCN listing of ‘least concern’. The positive flyway status of the European sub-species of white-fronted goose is not shared with the Greenland white-fronted goose, which is now fully protected and cannot be harvested in the UK. Greenland white-fronts come into Scotland, Northern Ireland, Northwest England and North Wales, while the European white-fronts tend to remain in England and are restricted to the East, South and Southwest. Due to this localised distribution, there is minimal potential for range overlap and the risk of lookalike shooting of the Greenland white-fronted goose is small. With already-low bag numbers in the UK, and scientific evidence of the species short stopping because of climatic changes, a cessation of shooting will have limited benefit. Continued low harvest of this species and collection of bag data, ring recovery information and wing survey details will contribute to our wider understanding of the species demographics and movement. Taking the above trend information, combined with the available science and evidence into consideration, BASC has provided the following recommendations:

Research required

  • Wintering surveys to better understand local and national distribution and
  • Submission of bag data is required to better inform harvest estimates (data can be submitted to GWCT National Gamebag Census or BASC Green Shoots Bagged It).
  • Shooters should support the BASC wing survey to enable better understanding of adult:juvenile harvest ratios.
  • Increased ringing, ring resighting and ring recovery reporting

Shooting restrictions

  • Two European white-fronts per person, per day, bag limit
  • It is the responsibility of all who shoot to correctly identify your If in doubt, don’t shoot.

Habitat management

  • Collaboration with agricultural managers in key feeding areas to ensure there is adequate feeding ground available.

Stage 2 assessment

Species summary

Two distinct greater white-fronted goose (WFG) sub-species occur in the UK, both of which are migratory and overwinter in different parts of the country; The Greenland WFG A.a. flavirostris, which breeds in west Greenland, stages in Iceland and overwinters primarily in Scotland1, Wales and Ireland, and the European WFG A. a. albifrons which breeds in north Europe and Asia, and overwinters in south and west Europe including England and Wales1. GWfG are no longer huntable quarry in the UK despite dedicated long-term conservation initiatives instigated by the shooting community that date back to 1972 in West Wales and Wales wide in 2012. There is already an International Single Species Action Plan for the Conservation of the Greenland White-fronted Goose, so this review will primarily focus on the European WFG which remains on Schedule II. NOTE: in some studies and reports the sub-species are not assessed separately. European white-fronted geese should be retained on Schedule II given the overall stable/increasing flyway trend. Changes in WFG distribution and numbers is predominantly driven by climate change and the resulting short-stopping behaviour, which may lead to a downturn in WFG numbers overwintering in the UK. However, the UK status and concern surrounding both WFG populations may lead to challenges surrounding this retention, BASC previously secured a moratorium with the wildfowling community on the shooting of all white-fronted geese in the North West of England to try and avoid the potential for misidentification in areas where both races could exist. The shooting of this species is infrequent within protected areas in England and Wales, with greater impacts outside of the wildfowling club structure. Therefore, efforts should focus on winter monitoring and bag recording across the entirety of the country and not just the foreshore areas.

Species conservation status (see Table 1)

The UK does not hold internationally important numbers of WFG2 (<1% of the global population3), however the small wintering European WFG population appears to be stable overall. Within the two countries it overwinters in, trends differ. The sub-species shows a decline of -15% in England and an increase of +10% in Wales between 2008-2018. The species has short and long term (5 and 25 year) WeBS alerts in England identifying declines on SPA’s >50% in the last 25 years4. European WFG is a notifiable species at only two SPAs in England (in Gloucestershire and Suffolk)4 however due to mixed trends there have been consenting conditions imposed at many sites where this is a feature species or part of a waterbird assemblage. Across the flyway, which is predominantly in Europe, the population appears stable and possibly increasing5,6.
BoCC8 (2020) IUCN UK8 (2020) Europe6 (2021) EU286 (2021) AEWA5 (2018) IUCN Global (Last updated in 2016)9
Category R EN LC (W) LC (W) European: C1 LC
Greenland: A2*
Trend (time period in brackets) Breeding: Stable Wintering: Decreasing Stable (over 3 generations) Increasing (over 3 generations) Stable (2009-2018) Unknown
Population size estimate Mature individuals Breeding: n/a Wintering: 14,000 Individuals10 1,180,000- 1,970,000 (min-max) 1,040,000- 1,570,000 (min-max) European: 1,000,000- 1,200,00011 Greenland: 21,50011 3,100,000- 3,200,000 (individuals)
Reason for category Severe non-breeding population decline over 25yrs/longer term. Non-breeding localisation. Reduction in the size (either abundance or range) of the wintering pop over 3 generations. Declines of 20-30% over 3 generations. n/a n/a European: Population >100,000 and could benefit from international cooperation but does not show declines, range contraction or data deficiency. Greenland: Population between 10-25,000 but hunting may continue on a sustainable basis. Large range, trend is not thought to be decreasing rapidly, large population size

WeBS UK 10-year tend (2008/09-2018/19): European -16%, Greenland -10%12 BBS UK 10-year trend (2010-2020): n/a**

Table 1. Species conservation status across different scales. *It has been highlighted by BASC that such automatic linkage between IUCN status and levels of protection by AEWA is directly contrary to the IUCN’s advice on the use of its list. **No Breeding Bird Survey data (BBS) as the species does not breed in in the UK.

Population dynamics

Historic and current research on WFG predominantly focusses on the Greenland WFG population which, following a recovery in the 1990’s due to hunting regulation, is now experiencing substantial, widespread decline as a result of poor breeding success7. Greenland WFG were removed from the quarry list in 2019 despite a widespread voluntary moratorium dating back to the 70’s in the Dyfi and c. 2012 across Wales. The European population lacks such in-depth research but currently shows different trends. The dichotomy of UK trends versus European trends creates a complex situation surrounding European WFG, particularly given that the decline is thought to be driven by climate change and resulting short-stopping behaviour3. The BoCC and UK IUCN listings merge the sub-species in recent reports, however supplementary material reveals both species were assessed separately but both classed as ‘Red’ and ‘Endangered’ as a result of long-term population trends8.

Hunting and harvest

European WFG shooting seasons in the UK are compliant with the Key Concepts of Article 7(4)13. WFG bag numbers over the last 20 years have been very low (<100) and as a result there is insufficient bag data on the species to estimate a trend in bag size or the sustainability of their harvest in the UK14,15. Overall, WFG experience limited hunting pressure within the UK, however, historically the highest bags have been in the former USSR, the Netherlands and Germany2. Greenland WFG may not be shot at all in the UK, this particularly affects Scotland and Ireland2, however this has resulted in the restriction of any ‘grey’ goose shooting on the Dyfi, Wales and may impact Anglesey. This action has, in part, been driven by a Conservation Strategy for the species led by AEWA which has called for full legal protection of Greenland WFG16. Given the primarily herbivorous nature of WFG, lead shot ingestion, is suggested not to be a major threat to the species17. Annual mortality in European WFG is relatively low, estimated around 25-30%2. However, hunting was previously stated as being the greatest driver of this mortality (around 80-95% of annual mortality)2.

Pressures, action and research

Pressures Climate change is likely the greatest driver of European WFG declines in the UK. With the UK being the most western extent of the species wintering range, the milder winters further north and east are thought to facilitate short-stopping and thus a decline in UK wintering numbers2,3,18,19. These climatic changes and shifts in other species distributions may eventually lead to competition with other species, such as Canada geese, for resources20. Given the localised distribution of wintering WFG populations in the UK, changes to these wetland sites and the surrounding agricultural land may be limiting the survival of migrant WFG9. European WFG are not considered major vectors of avian influenza compared to duck species21. Limited studies suggest WFG do not transmit the disease on long-distance migrations and stop-overs but rather contract it at wintering sites21. Practical action Given the localised distribution of wintering European WFG in the UK2, the conservation and improvement of over-wintering sites is key for the individuals that return to the UK each year9,18. This will be of paramount importance in severe winters where the species will likely extend the migration as far west as possible. Such habitat improvement may include collaboration with surrounding agricultural managers to ensure there is adequate feeding ground available. Continued monitoring of the species through WeBS surveys, as well as recording of any bag data is key to understanding the remaining wintering populations distribution and demographics. Research action Given the likelihood that UK declines are driven by climate change, a co-ordinated ringing/tagging programme is key to understanding distributional shifts and the exchange of individuals between flyways2. There is limited monitoring in eastern European countries where there are a number of remote WFG sites. Here, bio-logging methods as part of flyway-level project work, would provide some insight into their role in short-stopping and migration. Within the UK, monitoring changes to the wintering population and the agricultural feeding sites, which are predominantly unprotected, will provide greater insight into drivers of trends and priority areas for conservation actiion2.

References

  1. Eda, et al. Phylogenetic relationship of the Greater White-fronted Goose Anser albifrons subspecies wintering in the Palaearctic region. Ornithol Sci vol. 12 (2013).
  2. Hearn, D. Greater White-fronted Goose Anser albifrons albifrons (Baltic-North Sea population) in Britain 1960/61 – 1999/2000. (2004).
  3. Mitchell, et al. Trends in goose numbers wintering in Britain and Ireland, 1995 to 2008. Ornis Svec 20, 128–143 (2010).
  4. Woodward, I. D., Frost, T. M., Hammond, M. J. & Austin, G. E. Wetland Bird Survey Alerts 2016/2017: Changes in numbers of wintering waterbirds in the Constituent Countries of the United Kingdom, Special Protection Areas (SPAs), Sites of Special Scientific Interest (SSSIs) and Areas of Special Scientific interest (ASSIs). BTO Research Report 721. bto.org/webs-reporting-alerts (2019).
  5. Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) – Agreement Text and Annexes As amended by MOP8. (2022).
  6. BirdLife European Red List of Birds. https://op.europa.eu/en/publications. (2021) doi:10.2779/967570.
  7. Fox, D. et al. The rise and fall of Greenland White-fronted goose: A case study in international conservation. British Birds 99, 242–261 (2006).
  8. Stanbury, et al. The status of our bird populations: the fifth Birds of Conservation Concern in the United Kingdom, Channel Islands and Isle of Man and second IUCN Red List assessment of extinction risk for Great Britain. British Birds 114, 723–747 (2021).
  9. BirdLife Anser albifrons. The IUCN Red List of Threatened Species 2016. https://dx.doi.org/10.2305/IUCN.UK.2016-3.RLTS.T22679881A85980652.en (2016) doi:10.2305/IUCN.UK.2016.
  10. Woodward, et al. APEP 4: Population estimates of birds in Great Britain and the United Kingdom. British Birds 113, 69–104 (2020).
  11. Wetlands International. Waterbird Populations Portal. wpp.wetlands.org (2022).
  12. Frost, T. M. et al. Waterbirds in the UK 2019/20: The Wetland Bird Survey. (2021).
  13. Key concepts of Article 7(4) of Directive 79/409/EEC: Period of reproduction and prenuptial migration of Annex II bird species in the 28 Member States. (2014).
  14. Aebischer, N. J. Fifty-year trends in UK hunting bags of birds and mammals, and calibrated estimation of national bag size, using GWCT’s National Gamebag Eur J Wildl Res 65, (2019).
  15. Ellis, & Cameron, T. An initial assessment of the sustainability of waterbird harvest in the United Kingdom. bioRxiv (2022).
  16. Stroud, A., Fox, A. D., Urquhart, C. & Francis, I. S. International Single Species Action Plan for the Conservation of the Greenland White-fronted Goose (Anser albifrons flavirostris). www.snh.org.uk/speciesactionframework/default.asp (2012).
  17. Aloupi, M., Kazantzidis, S., Akriotis, T., Bantikou, E. & Hatzidaki, V. O. Lesser White-fronted (Anser erythropus) and Greater White-fronted (A. albifrons) Geese wintering in Greek wetlands are not threatened by Pb through shot ingestion. Science of the Total Environment 527–528, 279–286 (2015).
  18. Stichting BirdLife Europe, BirdLife International & Article 12 EU population status assessments: Annex B – Bird species’ status and trends report format (Article 12) for the period 2013 – 2018. (2020).
  19. BirdLife Anser anser. The IUCN Red List of Threatened Species 2018. https://dx.doi.org/10.2305/IUCN.UK.2018- (2018) doi:10.2305/IUCN.UK.2018.
  20. Fox, D. & Glahder, C. M. Post-moult distribution and abundance of white-fronted geese and Canada geese in West Greenland in 2007. Polar Res 29, 413–420 (2010).
  21. Yin, et al. No evidence that migratory geese disperse avian influenza viruses from breeding to wintering ground. PLoS One 12, (2017).

Eurasian Woodcock

Scolopax rusticola

2023-2028 Recommendation: delay shooting until late November where resident woodcock are present.

Species trend

The UK hosts a breeding population of woodcock which remains resident all year round, as well as hosting a large migrant over-wintering population. The breeding population has shown substantial declines in its range and size over the last 20 plus years. The migrant wintering population has, in contrast, increased over the last 25 years; this is reflected in the European IUCN listing of ‘least concern’.

Changes in climate, predation and habitat availability in the UK are likely driving the decline in the resident UK population and a number of conservation recommendations have been made by the GWCT to reduce negative impacts on the declining UK breeding population. Taking these into consideration, BASC has provided the following recommendations.

Research required

  • Breeding and wintering surveys to better understand local and national distribution and abundance.
  • Submission of bag data to better inform harvest estimates
  • (data can be submitted to the GWCT National Gamebag Census or BASC Green Shoots Bagged It).
  • Hunters should support the BASC wing survey to enable better understanding of adult:juvenile and male:female harvest ratios.

Shooting restrictions

  • Should avoid shooting woodcock in areas where resident woodcock are present until the major fall of migrant woodcock in late November.
  • Show restraint, even when resident birds are Shoot what you need, not what you can.
  • Shoot flightlines with
  • Curb shooting in severe

Habitat management

  • Targeted habitat creation and management for both breeding and wintering populations is required.
    • Create or widen woodland rides to provide breaks in the tree Ideally, rides should be at least 8m wide.
    • Mow rides and clearings to produce accessible grassy feeding and breeding display sites.
    • Create and reinstate clearings and young woodland using a little-but-often Over time this creates a mosaic of woodland types and ages.
    • Periodically remove marginal vegetation along sections of ditch or pond edges where these features occur within or close to woodlands.
    • Create wet features that retain ground moisture into late
  • Pest and predator
  • Refuge provision, either for set periods of time (temporal) or over dedicated areas of land (spatial), dependent on-site requirements.

Stage 2 assessment

Species summary

Official UK population trends of woodcock (particularly wintering population estimates) are limited due to the efficacy of the generic survey methods used. It is acknowledged, therefore, that woodcock numbers are being underestimated by surveyors1. GWCT-BTO species-specific surveys between 2003 and 2013 reported a 29% decline in breeding birds1.

Drivers of decline in the breeding populations size and extent are unclear but are likely a result of climate change, changes to habitat (especially woodland) management,

predation and possibly disturbance and shooting1. Estimates of wintering population trends are not available and considered hard to estimate due to survey difficulty.

Species conservation status (see Table 1)

The breeding (resident) UK population shows a decline of 29% between 2003-20131 (the next major survey will be in 20232). This is coupled with a range decline, particularly in the south and west of the UK1,3. It is however, important to note that this breeding population represents a very small proportion of the flyway’s breeding population4. However, in parallel, the large migrant wintering population is displaying a 25-year increase of 113%5. Woodcock have a large and widespread population across the entirety of their range and therefore, outside the UK, retain a favourable conservation status6,7. Although facing local pressures at breeding and wintering ground due to land use changes and climate change1,8–10, their distribution and migration routes are diffuse11, making the global population resilient12,13.

 

BoCC14

(2020)

IUCN UK14

(2020)

Europe6

(2021)

EU286

(2021)

AEWA4

(2018)

IUCN Global7 (Last updated in 2016)
CategoryRVULC (B)LC (B)B2cLC
Trend (time period in brackets)

Breeding: Decreasing1

(2003-2013)

Wintering: Increasing5

(1993/4 -2018/19)

Decreasing (over 3 generations)Decreasing (over 3 generations)

Decreasing

(2009-2018)

Stable
Population size estimate Mature individuals

Breeding: 57,000 Males

(95% CI: 43,000–71,000)

Wintering: 1,400,000 Individuals15

9,790,000-

13,500,000

(min-max)

1,410,000-

2,940,000

(min-max)

15,000,000-

20,000,000

(min-max)

10,000,000-

26,000,000

Reason for category

Severe breeding range decline over long term.

Moderate breeding range decline

over 25yrs14

Reduction in size (either abundance or range) of

breeding & non-breeding population.

Declines between 20-30% over 3 generations14

n/an/a

Populations numbering more than around 100,000

individuals, considered in need of special attention as a result of showing long-term decline4

n/a
WeBS UK 10-year tend (2008/09-2018/19): n/a  ● BBS UK 10-year trend (2010-2020): n/a**

Table 1. Species conservation status across different scales. *It has been highlighted by BASC that such automatic linkage between IUCN status and levels of protection by AEWA is directly contrary to the IUCN’s advice on the use of its list. **Due to its cryptic nature this species cannot be surveyed using standard methods. A woodcock-specific survey has replaced this.

Population dynamics

Woodcock populations are often estimated by the number of ‘roding’ (displaying) males during the breeding season1,16. This survey data is then extrapolated to estimate overall population size. Winter surveys are more challenging due to the cryptic nature of woodcock and absence of displaying. Female woodcock rear broods alone, using different habitat for incubation and foraging10. It is unclear whether reproductive success and recruitment are driving the breeding population decline, or if it is a result of poor adult survival. These aspects of woodcock population dynamics therefore require further investigation.

Hunting and harvest (see Table 2)

Woodcock shooting seasons in the UK are compliant with the Key Concepts of Article 7(4)17. Woodcock are a popular species to hunt in the UK with some of the highest bag numbers of all recorded quarry species18. Bag numbers have remained relatively stable since the 90’s but have been gradually decreasing since 200419. It is unclear if this relates to voluntary restraint or a population decline. Woodcock are estimated to have a sustainable harvest in the UK for both migrant and resident birds, however the estimates of Sustainable Harvest Index (SHI) have wide confidence intervals and require more accurate population estimates and understanding of origin and age composition of birds shot20. Woodcock are legally hunted in 26 countries in Europe. Bag data from 21 of these countries estimate the total harvest to be over 970,000 birds21. Bag sizes were historically largest in France, Greece, Ireland, the UK and Italy22.

Species

Species estimated

λmax (95% CI)

Potential excess growth (95% CI)Mean Sustainable Hunt Index (95% CI)Probability of unsustainable harvest
Woodcock (Resident)

1.411

(1.302 – 1.61)

28,000

(16,000 – 46,000)

0.711

(0.394 – 1.183)

0.097
Woodcock (Migratory)

1.411

(1.302 – 1.61)

210,000

(120,000 – 340,000)

0.636

(0.353 – 1.057)

0.042

Table 2. Estimated sustainability of species harvest in the UK. Table from Ellis & Cameron 2022.

Little is known about the impact of disturbance on woodcock, either in the form of hunting or other outdoor activities23. It is suggested that hunting mortality may locally impact the over-winter survival of woodcock24 but this is hard to quantify, especially in the UK where migrant birds substantially outnumber residents1. Overall, woodcock appear to retain site fidelity after disturbance if there is access to high quality foraging areas23, highlighting the importance of meadow and grassland bordering woodland habitat.

Pressures, action and research

Pressures

Climate change is considered a driver in range shifts and survival of woodcock and other woodland birds8. Within the UK this is likely exacerbated by agricultural practices to increase yield, such as drainage of soil, increased fertilisers and loss of pasture and grassland9. Forestry management such as ride and glade creation and coppicing has been replaced by commercial timber production. Reduced variation of age structure in woodland and increased woodland fragmentation is also considered a major driver of woodcock decline1,10. Alongside habitat changes driven by deer as well as humans, increased predation by mustelids, feral cats, foxes and raptors is also thought to play a role in the species decline23,25–27.

Practical action

Habitat restoration, through adaptation of agricultural and forestry activities is the primary action recommended to support woodcock populations10,28,29. Many of these actions require financial incentivisation and it is possible improvements may be seen in coming years due to increased tree planting for carbon capture. Current action also includes voluntary restraint of shooting early in the season and predator control30. However, the impact of these activities (or change in their intensity) has not been documented.

Research action

Data collection on demographics of shot birds/hunting effort can be improved through increased participation in the National Game Bag Census (GWCT) and Wing Survey (BASC). Increased survey effort of winter and breeding populations across the UK and Ireland will also help establish on a long-term, species-specific dataset2 (BTO/GWCT). Focused research is required to build on some of the more complex aspects considered to impact woodcock such as predation25 and the associated predator control, disturbance by various recreational activities23, the impact of deer damage on woodcock and their habitat1,10,26 and the role of hunting relative to other forms of mortality28,31.

References

  1. Heward, J. et al. Current status and recent trend of the Eurasian Woodcock Scolopax rusticola as a breeding bird in Britain. Bird Study 62, 535–551 (2015).
  2. GWCT & BTO. GWCT/BTO Breeding Woodcock Survey 2021. (2021).
  3. Balmer, D. E. et al. Bird Atlas 2007-11: the breeding and wintering birds of Britain and Ireland. (2013).
  4. Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) – Agreement Text and Annexes As amended by MOP8. (2022).
  5. Frost, T. M. et al. Waterbirds in the UK 2019/20: The Wetland Bird Survey. (2021).
  6. BirdLife European Red List of Birds. https://op.europa.eu/en/publications. (2021) doi:10.2779/967570.
  7. BirdLife International. Scolopax rusticola (amended version of 2016 assessment). (2019).
  8. Leech, I. & Crick, H. Q. P. Influence of climate change on the abundance, distribution and phenology of woodland bird species in temperate regions. Ibis 149, 128–145 (2007).
  9. Duriez, et al. Habitat selection of the Eurasian woodcock in winter in relation to earthworms availability. Biol Conserv 122, 479–490 (2005).
  10. Hoodless, N. & Hirons, G. J. M. Habitat selection and foraging behaviour of breeding Eurasian Woodcock Scolopax rusticola : a comparison between contrasting landscapes. Ibis (2007).
  11. EURING Migration Migratory connectivity analysis by EURING Migration Atlas – Scolopax rusticola (05290).
  12. Cohen, B. et al. Quantifying the strength of migratory connectivity. Methods Ecol Evol 9, 513–524 (2018).
  13. Powell, A. Origins and non-breeding ecology of Eurasian woodcock. (Oxford University, 2013).
  14. Stanbury, et al. The status of our bird populations: the fifth Birds of Conservation Concern in the United Kingdom, Channel Islands and Isle of Man and second IUCN Red List assessment of extinction risk for Great Britain. British Birds 114, 723–747 (2021).
  15. Woodward, et al. APEP 4: Population estimates of birds in Great Britain and the United Kingdom. British Birds 113, 69–104 (2020).
  16. Hoodless, N., Lang, D., Aebischer, N. J., Fuller, R. J. & Ewald, J. A. Densities and population estimates of breeding Eurasian Woodcock sco/opax rusticola in Britain in 2003. Bird Study vol. 56 15–25 Preprint at https://doi.org/10.1080/00063650802674768 (2009).
  17. Key concepts of Article 7(4) of Directive 79/409/EEC: Period of reproduction and prenuptial migration of Annex II bird species in the 28 Member States. (2014).
  18. Aebischer, N. J. Fifty-year trends in UK hunting bags of birds and mammals, and calibrated estimation of national bag size, using GWCT’s National Gamebag Eur J Wildl Res 65, (2019).
  19. Game and Wildlife Conservation Trust. Bird bags – summary trends: Woodcock Scolopax rusticola. https://www.gwct.org.uk/research/long-term-monitoring/national-gamebag-census/bird-bags-summary-trends/woodcock/ (2006).
  20. Ellis, & Cameron, T. An initial assessment of the sustainability of waterbird harvest in the United Kingdom. bioRxiv (2022).
  21. Hirschfeld, A., Attard, G. & Scott, L. Bird hunting in Europe: an analysis of bag figures and the potential impact on the conservation of threatened British Birds 112, 153–166 (2019).
  22. Hirschfield, A. & Heyd, A. Mortality of migratory birds caused by hunting in Europe: bag statistics and proposals for the conservation of birds and animal Ber. Vogelschutz 42, 47–74 (2005).
  23. Ferrand, , Aubry, P., Landry, P. & Priol, P. Responses of Eurasian woodcock Scolopax rusticola to simulated hunting disturbance. Wildlife Biol 19, 19–29 (2013).
  24. Duriez, , Fritz, H., Said, S. & Ferrand, Y. Wintering behaviour and spatial ecology of Eurasian Woodcock Scolopax rusticola in western France. Ibis vol. 147 (2005).
  25. Braña, F., Prieto, L. & González-Quirós, P. Habitat change and timing of dusk flight in the Eurasian woodcock: a trade-off between feeding and predator avoidance? Zool. Fennici 47, 206–214 (2010).
  26. Holt, & Fuller, R. An experimental assessment of the effect of deer on use of young coppiced woodland by Eurasian Woodcocks in winter. Wader Study Group Bulletin 120, 124–127 (2013).
  27. Ferrand, Y. Sixth European Woodcock and Snipe Workshop. in Proceedings of an International Symposium of the Wetlands International Woodcock and Snipe Specialist Group 25–27 November 2003, Nantes, France. International Wader Studies 13, Wageningen, The Netherlands 114 (Australasian Wader Studies Group, 2006).
  28. Stichting BirdLife Europe, BirdLife International & Article 12 EU population status assessments: Annex B – Bird species’ status and trends report format (Article 12) for the period 2013 – 2018. (2020).
  29. Bellamy, E. et al. Impact of woodland agri-environment management on woodland structure and target bird species. J Environ Manage 316, (2022).
  30. Brewin, , Hoodless, A. N., Heward, C. J. & Hopgood, A. 2022. Conserving Our Woodcock: Research-based measures to help the UK’s resident population. www.gwct.org.uk (2022).
  31. Duriez, O., Eraud, C., Barbraud, C. & Ferrand, Y. Factors affecting population dynamics of Eurasian woodcocks wintering in France: Assessing the efficiency of a hunting-free Biol Conserv 122, 89–97 (2005).
  32. UK Government and Parliament Ban the Shooting of Critically Endangered Woodcocks: Closed petition. https://petition.parliament.uk/petitions/595483?reveal_response=yes (2021).
  33. UK Government and Parliament Limit the shooting season of woodcock: Petition. https://petition.parliament.uk/petitions/619615 (2022).

Common Snipe

Gallinago gallinago 2023-2028 Recommendation: delay shooting until September where resident breeding common snipe are present. 

Species trend

The UK hosts a breeding population of common snipe which remains resident all year round, as well as hosting a large migrant overwintering population. The breeding population has experienced a marginal decline, while the wintering population has shown a more moderate decline. However, due to the large range and relatively high abundance, snipe are not yet considered ‘vulnerable’. Changes in snipe populations in the UK and Europe are primarily attributed to agricultural changes. Although there is no evidence that shooting is driving this decline, the current snipe shooting season opening date of 12 August (England, Wales, and Scotland) crosses over with the species breeding period. Management for other game birds, such as predator control, has been beneficial for snipe, and recovery of ringed birds by shooters has contributed to knowledge surrounding migration and movement of snipe. Therefore, continued bag reporting and participation in ringing studies are important roles for the shooting community. Taking the above information into consideration, BASC has provided the following recommendations:

Research required

  • Focused studies on snipe as opposed to lowland waders, as snipe are often missed in traditional survey techniques.
  • Submission of bag data is required to better inform harvest estimates (data can be submitted to GWCT National Gamebag Census or BASC Green Shoots Bagged It).
  • Shooters should support the BASC wing survey to enable better understanding of adult:juvenile ratios.
  • Increased ringing, ring resighting, and ring recovery reporting
  • Research into habitat factors that may be influencing snipe declines, such as food
  • Greater understanding of recruitment is required to help disentangle habitat-mediated pressures from productivity issues.

Shooting restrictions

  • Should avoid shooting common snipe in areas where resident breeding snipe are present until 1 September
  • Show restraint, even when resident birds are Shoot what you need, not what you can
  • Curb shooting in severe

Habitat management

  • Habitat management for both breeding and wintering populations is required:
    • Raise water levels to create wetter
    • Reduce grazing pressure around breeding
    • Scrape creation and rush
  • Pest and predator
  • Refuge provision; minimise disturbance either for set periods of time (temporal), or over dedicated areas of land (spatial) dependent on site requirements.

Stage 2 assessment

Species summary

Changes in snipe populations in the UK and Europe are primarily attributed to agricultural changes, however conservation efforts that have enabled recovery by other wading species have not been effective for snipe6–8. There is no evidence that shooting is driving this decline, and management for other game birds, such as predator control, has been beneficial for snipe9. The shooting community should continue to play a role in this species management as well as sharing bag returns and ring recoveries.

Species conservation status (see Table 1)

The common snipe (hereafter snipe) population shows a 10-year wintering population decline in the UK >25% between 2008-20181. Within the UK countries this trend is mixed, with Scotland, England and Northern Ireland experiencing significant wintering population declines (-43%, -28% and -41% respectively) compared to a slight increase in numbers in Wales (+3%)1. Breeding populations show a different pattern however, displaying only a marginal decline in the overall UK population (-2.39%), with large breeding population increases in England (+43%)2. Only 35% of the species global range is within Europe3, however this decline is reflected on the European continent within breeding populations and is anticipated to continue4. At a global scale, due to its large range and relatively high abundance, snipe are not yet considered ‘Vulnerable’ to extinction5.
BoCC10 (2020) IUCN UK10 (2020) Europe4 (2021) EU284 (2021) AEWA11 (2018) IUCN Global (Last updated in 2017)
Category A VU VU (B) LC (B) B2c LC
Trend (time period in brackets) Decreasing (2008/09-2018/19) Decreasing (over 3 generations) Decreasing (over 3 generations) European: Decreasing/ Stable Icelandic: Decreasing(?) (2009-2018) Decreasing
Population size estimate Mature individuals Breeding: 66,500 pairs Wintering: 1,100,000 Individuals12 5,270,000- 7,260,000 (min-max) 844,000- 1,520,000 (min-max) European: 7,000,000- 10,000,000 Icelandic: 1,100,000- 1,100,000 (min-max) 15,000,000- 29,000,000
Reason for category Threatened in Europe Moderate non-breeding pop decline over 25yrs Moderate breeding range decline over longer term Reduction in size of non-breeding pop. (either abundance or range) over 3 generations. Declines of 20- 30% over 3 generations. Population reduction observed & projected. Causes of reduction may not have ceased OR may not be understood OR may not be reversible. n/a Population >100,000 individuals but considered in need of special attention due to long-term decline. Due to a large range and large population size, combined with a <30% decline over 3 generations, the population does not approach thresholds for ‘Vulnerable’
WeBS UK 10-year trend (2008/09-2018/19): -27%1 ● BBS UK 10-year trend (2010-2020): -2.39%2
Table 1. Species conservation status across different scales. *It has been highlighted by BASC that such automatic linkage between IUCN status and levels of protection by AEWA is directly contrary to the IUCN’s advice on the use of its list.

Population dynamics

The snipe population continues to slowly decline across its range and lacks recent, focussed research on non-agricultural factors that may be impacting its population trend. Further research is required into predation, nesting success and chick survival. This research needs to be undertaken independently of, and alongside, habitat management that is currently implemented. Hunting and harvest (see Table 2) The snipe shooting seasons in the UK are not compliant with the Key Concepts of Article 7(4)13. The start date of the open season in Scotland (12th August) overlaps with the estimated end of the reproduction period for snipe in the north of the UK by two ‘decades’ (approx. 20 days). This is therefore in breach of the agreement. Snipe has a moderately large game bag in the UK, with high but declining bag numbers in recent years (2004: 64,000, 2012: 100,000, 2016: 85,000) that is reflective of the population decline14,15. However, given its high population size in the UK, it is unlikely that this harvest level is unsustainable16. France, Ireland and the UK appear to have the largest reported bag numbers within Europe17.
Species Species estimated λmax (95% CI) Potential excess growth (95% CI) Mean Sustainable Hunt Index (95% CI) Probability of unsustainable harvest
Common snipe 1.467 (1.336 – 1.732) 210,000 (140,000 – 320,000) 0.392 (0.133 – 0.763) 0.000
Table 2. Estimated sustainability of species harvest in the UK. Table from Ellis & Cameron 2022. Limited studies suggest snipe may be sensitive to disturbance caused by shore-side and marshland hunting, therefore spatial restrictions on shooting and provision of refuges, as opposed to temporal restrictions, are likely to be beneficial to wintering snipe in the UK18. Recovery of ringed birds by hunters has contributed to knowledge surrounding migration and movement of snipe, therefore continued bag reporting and participation in ringing studies are important roles for the shooting community19–21.

Pressures, action and research

Pressures The drivers of snipe declines are unclear. Overall declines in wading birds are predominantly attributed to changes in agricultural practices and land use22. These changes include increased drainage3,23,24, improvement of marginal grassland23,25, intensification of grazing23,24 and increased use of fertilisers22. However, given the conservation measures employed since the 1990’s and continued decline of snipe, it is possible that these factors are not the main drivers of snipe declines. Predation, particularly of nesting birds, is suggested to be a major contributor to lack of snipe recovery26–30. Practical action A number of changes to agricultural management have already been undertaken through agri-environment schemes, such as raising water levels and creating wetter fields31, reducing grazing pressure around wader breeding sites, scrape creation and rush management23,32. In upland areas, re-wetting programmes are also likely to be beneficial to snipe, although this species is understudied in moorland habitats24. As for many ground-nesting waders, predator control is likely to improve breeding success of snipe, however trials so far have had mixed effects 8,9,23,30. Reduced disturbance of snipe, through provision of refuges during shooting seasons is also recommended18,22 alongside overall wetland restoration. Research action Studies on migratory populations may reveal changes to migratory routes related to climate change which is in turn impacting wintering populations in the UK. Research into habitat factors that may be influencing snipe declines such as prey abundance are required to help understand why current conservation action is not benefiting snipe populations. Increased, focussed studies on snipe as opposed to ‘lowland waders’ as a collective will allow for snipe-specific surveying and monitoring as they are often missed in traditional bird surveys33. This work should focus on chick survival and nesting predation during the breeding season6. Predator control, alongside intensive nest monitoring would provide good evidence as to the efficacy of this management on snipe populations. Greater understanding of recruitment is required to help disentangle habitat-mediated pressures from productivity issues.

References

  1. Frost, T. M. et al. Waterbirds in the UK 2019/20: The Wetland Bird Survey. (2021).
  2. Harris, S. J. et al. The Breeding Bird Survey 2021. BTO Research Report 745. bto.org (2022).
  3. Birdlife Gallinago gallinago (amended version of 2017 assessment). The IUCN Red List of Threatened Species 2019. http://dx.doi.org/10.2305/IUCN.UK.2019-3.RLTS.T22693097A155504420.en (2019) doi:10.2305/IUCN.UK.2019-3.RLTS.T22693097A155504420.en.
  4. BirdLife European Red List of Birds. https://op.europa.eu/en/publications. (2021) doi:10.2779/967570.
  5. Anas The IUCN Red List of Threatened Species 2019: e.T22680301A153882797. https://dx.doi.org/10.2305/IUCN.UK.2019-3.RLTS.T22680301A153882797.en (2019) doi:10.2305/IUCN.UK.2019.
  6. Smart, J., Amar, A., O’Brien, M., Grice, P. & Smith, K. Changing land management of lowland wet grasslands of the UK: Impacts on snipe abundance and habitat Anim Conserv 11, 339–351 (2008).
  7. Kelly, L. A., Douglas, D. J. T., Shurmer, M. P. & Evans, K. L. Upland rush management advocated by agri-environment schemes increases predation of artificial wader Anim Conserv 24, 646–658 (2021).
  8. Fletcher, , Aebischer, N. J., Baines, D., Foster, R. & Hoodless, A. N. Changes in breeding success and abundance of ground-nesting moorland birds in relation to the experimental deployment of legal predator control. Journal of Applied Ecology 47, 263–272 (2010).
  9. Ludwig, C., Roos, S. & Baines, D. Responses of breeding waders to restoration of grouse management on a moor in South-West Scotland. J Ornithol 160, 789–797 (2019).
  10. Stanbury, et al. The status of our bird populations: the fifth Birds of Conservation Concern in the United Kingdom, Channel Islands and Isle of Man and second IUCN Red List assessment of extinction risk for Great Britain. British Birds 114, 723–747 (2021).
  11. Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) – Agreement Text and Annexes As amended by MOP8. (2022).
  12. Woodward, et al. APEP 4: Population estimates of birds in Great Britain and the United Kingdom. British Birds 113, 69–104 (2020).
  13. Key concepts of Article 7(4) of Directive 79/409/EEC: Period of reproduction and prenuptial migration of Annex II bird species in the 28 Member States. (2014).
  14. Kahlert, J., Fox, A. D., Heldbjerg, H., Asferg, T. & Sunde, P. Functional Responses of Human Hunters to Their Prey-Why Harvest Statistics may not Always Reflect Changes in Prey Population Wildlife Biol 21, 294–302 (2015).
  15. Aebischer, N. J. Fifty-year trends in UK hunting bags of birds and mammals, and calibrated estimation of national bag size, using GWCT’s National Gamebag Eur J Wildl Res 65, (2019).
  16. Ellis, & Cameron, T. An initial assessment of the sustainability of waterbird harvest in the United Kingdom. bioRxiv (2022).
  17. Hirschfield, A. & Heyd, A. Mortality of migratory birds caused by hunting in Europe: bag statistics and proposals for the conservation of birds and animal Ber. Vogelschutz 42, 47–74 (2005).
  18. Bregnballe, , Madsen, J. & Rasmussen, P. A. F. Effects of temporal and spatial hunting control in waterbird reserves. Biol Conserv 119, 93–104 (2004).
  19. Meissner, Ringing recoveries of the common snipe (Gallinago gallinago) caught during autumn migration in the Gulf of Gdansk region. The Ring 24, (2002).
  20. Musgrove, J. et al. Overwinter population estimates of British waterbirds. British Birds 104, 364–397 (2011).
  21. Péron, , Ferrand, Y., Leray, G. & Gimenez, O. Waterbird demography as indicator of wetland health: The French-wintering common snipe population. Biol Conserv 164, 123–128 (2013).
  22. Stichting BirdLife Europe, BirdLife International & Article 12 EU population status assessments: Annex B – Bird species’ status and trends report format (Article 12) for the period 2013 – 2018. (2020).
  23. Colhoun, , Mawhinney, K. & Peach, W. J. Population estimates and changes in abundance of breeding waders in Northern Ireland up to 2013. Bird Study 62, 394–403 (2015).
  24. Hoodless, N., Ewald, J. A. & Baines, D. Habitat use and diet of Common Snipe Gallinago gallinago breeding on moorland in northern England. Bird Study 54, 182–191 (2007).
  25. Fuller, J., Ward, E., Hird, D. & Brown, A. F. Declines of ground-nesting birds in two areas of upland farmland in the south pennines of england: We present evidence of large declines in numbers of breeding waders and passerines in some upland areas since the 1970s. Bird Study 49, 146–152 (2002).
  26. Macdonald, M. A. & Bolton, M. Predation on wader nests in Europe. Ibis vol. 150 (2008).
  27. Roodbergen, , van der Werf, B. & Hötker, H. Revealing the contributions of reproduction and survival to the Europe-wide decline in meadow birds: Review and meta-analysis. Journal of Ornithology vol. 153 53–74 Preprint at https://doi.org/10.1007/s10336-011-0733-y (2012).
  28. Laidlaw, A. et al. Vegetation structure influences predation rates of early nests in subarctic breeding waders. Ibis 162, 1225–1236 (2020).
  29. Rodrigues, M., Rodrigues, M. & Gonçalves, D. Breeding phenology and success of the Common Snipe Gallinago gallinago in the Azores. Bird Study 66, 441–451 (2019).
  30. Jellesmark, et al. The effect of conservation interventions on the abundance of breeding waders within nature reserves in the United Kingdom. Ibis (2022) doi:10.1111/ibi.13106.
  31. Buchanan, M., Pearce-Higgins, J. W., Douglas, D. J. T. & Grant, M. C. Quantifying the importance of multi-scale management and environmental variables on moorland bird abundance. Ibis 159, 744–756 (2017).
  32. Holton N & Allcorn The effectiveness of opening up rush patches on encouraging breeding common snipe Gallinago gallinago at Rogersceugh Farm, Campfield Marsh RSPB reserve, Cumbria, England. Conservation Evidence vol. 3 www.ConservationEvidence.com (2006).
  33. Hoodless, N., Inglis, J. G. & Baines, D. Effects of weather and timing on counts of breeding Snipe Gallinago gallinago. Bird Study 53, 205–212 (2006).

Eurasian Coot

Fulica atra Recommendation: research required.

Species trend

The UK breeding population shows a substantial ten-year decline of 24-44 per cent between 2010-2020. This is mirrored in a wintering population decline of 24 per cent; as a result they are listed as ‘near threatened’ on the European IUCN Red List. Although widespread, coots, like moorhens, remain relatively under-studied, particularly in relation to their movement and population demographics. Ringing studies show that coots do migrate within the UK as well as between the UK and central Europe/Russia. The species receives very little shooting pressure in the UK and its popularity as a quarry species is decreasing across the flyway. Therefore, shooting is unlikely to be driving declines. Coots likely suffer from multiple pressures driven by habitat and climate change, but their flexible behaviour and ability to adapt may have diluted any obvious impacts. Shooting restrictions are unlikely to have any benefit. Instead, research investment to better understand the causes of ongoing declines is necessary, alongside habitat management and conservation interventions.

Research required

  • Breeding and wintering surveys to better understand local and national distribution and abundance.
  • Submission of bag data to better inform harvest estimates (data can be submitted to the GWCT National Gamebag Census or BASC Green Shoots Bagged It).
  • Shooters should support the BASC wing survey to enable better understanding of adult:juvenile harvest ratios.
  • Increased ringing and ring resighting effort to improve understanding of migratory

Shooting restrictions

  • Should show
  • Site-based considerations

Habitat management

  • General wetland creation and management will benefit both breeding and wintering
  • A mosaic habitat of dense cover, open water and clearings is required to provide safe refuge and feeding areas.
  • Ensure suitable breeding sites have ramp-like areas to enable chicks to leave the water easily.
  • Pest and predator
  • Refuge provision, either for set periods of time (temporal) or over dedicated areas of land (spatial), dependent on site requirements.
  • Nesting support (for example: fencing, duck nest tubes, provision of maintained islands).

Stage 2 assessment

Species summary

Although widespread, coot, like moorhen, remain relatively under-studied, particularly in relation to their movement and population demographics. Ringing studies show that coot do migrate within the UK as well as between the UK and central Europe/Russia1. However, drivers of population declines are unclear and require further research. Coot likely suffer from multiple pressures driven by habitat and climate change, but their flexible behaviour and ability to adapt may have diluted any obvious impacts. The species receives very little hunting pressure in the UK and its popularity as a quarry species is decreasing across the flyway. The species requires greater research investment to understand the causes of ongoing declines.

Species conservation status (see Table 1)

The UK breeding population of coot shows a substantial 10-year decline in both BBS surveys (-24.47% between 2010-2020) and WBBS surveys (-44% 2010-2020)2. This is mirrored in the wintering population trend (-24%)3. The breeding population is predominantly concentrated in England and therefore is the only country with breeding data trends (-21.18% over 10 years)2. The wintering population trends are very mixed, with declines in England (-29%) and Wales (-29%) and increases in Northern Ireland (+111%) and Scotland (+6%)3. The coot has amber WeBS alerts in Northern Ireland and Scotland due to long-term population declines (over 25 years) and in Wales due to 10-year declines4. This broad trend is shared across Europe, however some populations are driving a stable trend in the EU5. At a global scale, the overall population trend is increasing but comprises mixed trends across the range6.
BoCC7 (2020) IUCN UK7 (2020) Europe5 (2021) EU285 (2021) AEWA8 (2018) IUCN Global6 (Last updated in 2019)
Category G VU NT (B) LC B2c LC
Trend (time period in brackets) Decreasing (Breeding and Wintering) Decreasing (over 3 generations) Stable (over 3 generations) Decreasing (2009-2018) Increasing
Population size estimate Mature individuals Breeding: 26,000+ Pairs Wintering: 205,000 Individuals9 2,030,000- 3,360,000 (min-max) 1,080,000, 1,720,000 (min-max) 1,200,000- 1,900,000 (min-max) 5,300,000- 6,500,000
Reason for category n/a Reduction in size of breeding pop & Non-breeding pop size (either abundance or range) measured over 3 generations. Declines 20% – 30% over 3 generations. Population reduction observed or suspected in the past where causes of reduction may not have ceased/may not be understood. Decline projected to continue. n/a Population >100,000 but is need of special attention as a result of long-term decline. Population has large range and size. Trend is increasing.

WeBS UK 10-year trend (2008/09-2018/19): -24%3 ● BBS UK 10-year trend (2010-2020): -24.47%2

Table 1. Species conservation status across different scales. *It has been highlighted by BASC that such automatic linkage between IUCN status and levels of protection by AEWA is directly contrary to the IUCN’s advice on the use of its list.

Population dynamics

The resident UK population is supplemented by continental birds during winter months10. However, outside of some foraging and behavioural research, very little is known about coot population dynamics. Ringing studies in France suggest adult survival is higher than juvenile survival, a common feature in waterbirds10. Of the adults, male survival is greater10. This is often attributed to greater female mortality during incubation, yet coot share the incubation of eggs therefore differences in survival must be driven by alternative pressures10. Potentially poor chick and juvenile survival is suggested to be a result of predation or low food availability11,12.

Hunting and harvest

The coot shooting seasons in the UK are not compliant with the Key Concepts of Article 7(4)13. The start date of the open season in England, Wales and Scotland (1st Sept) overlaps with the estimated end of the reproduction period for coot in the south of the UK by one ‘decade’ (approx. 10 days), and by three decades (approx. 30 days) in Scotland. This is therefore in breach of the agreement. Take of coot is already prohibited in Northern Ireland and the Isle of Man. There is no bag data available for coot in the rest of the UK. The species is rarely harvested and as a result there is no modern estimates of its harvest (nor the sustainability of this harvest). It is suggested that coot have become a less popular quarry over time in Europe too10. Recreational hunting appears to displace coots from their preferred feeding grounds to sub-optimal habitat, for example deep water14,15. This is likely detrimental to coots as they feed during the day and cannot compensate for feeding disturbance at night due to their visual foraging strategy14,16,17. Refuges that are not shot over or disturbed by humans for other recreational activities, such as fishing, would likely reduce disturbance to coot14,18. Coot show low prevalence of lead shot ingestion, likely due to their feeding strategy19, feeding primarily on submerged algae and invertebrates they have brought to the surface17.

Pressures, action and research

Pressures Coot remain a fairly under-studied species, particularly in relation to their movement and population dynamics10,20. However, predation is suggested to be a major contributor to coot declines in Europe due to the spread of invasive American mink21–23. Competition with fish in commercial carp ponds may reduce habitat available to coot in central and Eastern Europe24. Climate change is also impacting coot laying dates and may, with time, result in phenological mis-matching between chick hatching and food abundance (predominantly dipterans)25. Coot also appear to suffer population declines after severe winters26, which may impact populations if winters become more severe. However, if winters become milder this may benefit the species26. Practical action Ensuring wintering, breeding and refuge sites have a high, year-round food abundance will benefit coot14,18. High food abundance is particularly important for chick survival12. This can be achieved through reedbed creation and planting or revegetation programmes that enhance submerged and emergent vegetation27. Predator control, particularly of crows and mink will benefit nesting coot as well as other waterbirds21,23,28. Removal of adult fish to allow for increased macrophyte growth will likely benefit coot in areas where there is a high concentration of aquaculture6. Research action There is limited understanding of coot movement, population demographics and migration. Knowledge of the species could be improved through ringing or marking programmes that allow for capture-mark-recapture studies10.

References

  1. Robinson, A., Leech, D. I. & Clark, J. A. The Online Demography Report: Bird ringing and nest recording in Britain & Ireland in 2021. (2022).
  2. Harris, S. J. et al. The Breeding Bird Survey 2021. BTO Research Report 745. bto.org (2022).
  3. Frost, T. M. et al. Waterbirds in the UK 2019/20: The Wetland Bird Survey. (2021).
  4. Woodward, D., Frost, T. M., Hammond, M. J. & Austin, G. E. Wetland Bird Survey Alerts 2016/2017: Changes in numbers of wintering waterbirds in the Constituent Countries of the United Kingdom, Special Protection Areas (SPAs), Sites of Special Scientific Interest (SSSIs) and Areas of Special Scientific interest (ASSIs). BTO Research Report 721. www.bto.org/webs-reporting-alerts (2019).
  5. BirdLife European Red List of Birds. https://op.europa.eu/en/publications. (2021) doi:10.2779/967570.
  6. BirdLife Fulica atra. The IUCN Red List of Threatened Species 2019. http://dx.doi.org/10.2305/IUCN.UK.2019- (2019) doi:10.2305/IUCN.UK.2019.
  7. Stanbury, et al. The status of our bird populations: the fifth Birds of Conservation Concern in the United Kingdom, Channel Islands and Isle of Man and second IUCN Red List assessment of extinction risk for Great Britain. British Birds 114, 723–747 (2021).
  8. Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) – Agreement Text and Annexes As amended by MOP8. (2022).
  9. Woodward, et al. APEP 4: Population estimates of birds in Great Britain and the United Kingdom. British Birds 113, 69–104 (2020).
  10. Guillemain, , Devineau, O., Simon, G. & Gauthier-Clerc, M. Common but poorly known: Information derived from 32 years of ringing Coot Fulica atra in the Camargue, southern France. Ringing and Migration 29, 10–18 (2014).
  11. Rȩk, Testing the relationship between clutch size and brood size in the Coot (Fulica atra). J Ornithol 151, 163–168 (2010).
  12. Brinkhof, & Cave, A. J. Food supply and seasonal variation in breeding success : an experiment in the European coot. Proceedings of the Royal Society London B 264, 291–296 (1997).
  13. Key concepts of Article 7(4) of Directive 79/409/EEC: Period of reproduction and prenuptial migration of Annex II bird species in the 28 Member States. (2014).
  14. Holm, E., Laursen, K. & Clausen, P. The feeding ecology and distribution of common coots Fulica atra are affected by hunting taking place in adjacent areas. Bird Study 58, 321–329 (2011).
  15. Evans, M. & Day, K. R. Hunting disturbance on a large shallow lake: the effectiveness of waterfowl refuges. Ibis vol. 144 (2002).
  16. Draulans, & Vanherck, L. Food and foraging of Coot Fulica atra on fish ponds during autumn migration. Wildfowl 38, 63–69 (1987).
  17. Irwin, & O’halloran, J. The wintering behaviour of coot Fulica atra l. at Cork Lough, South-west Ireland. Biology and environment: Proceedings of the royal Irish academy 97B, 157–162 (1997).
  18. Quan, -C., Wen, X. & Yang, X. Effects of human activities on migratory waterbirds at Lashihai Lake, China. Biol Conserv 108, 273–279 (2002).
  19. Mateo, , Guitart, R. & Green, A. J. Determinants of Lead Shot, Rice, and Grit Ingestion in Ducks and Coots. J Wildl Manage 64, 939–947 (2000).
  20. Binkowski, J., Sawicka-Kapusta, K., Szarek, J., Strzyzewska, E. & Felsmann, M. Histopathology of liver and kidneys of wild living Mallards Anas platyrhynchos and Coots Fulica atra with considerable concentrations of lead and cadmium. Science of the Total Environment 450–451, 326–333 (2013).
  21. Brzeziński, M., Natorff, M., Zalewski, A. & Z̈mihorski, M. Numerical and behavioral responses of waterfowl to the invasive American mink: A conservation Biol Conserv 147, 68–78 (2012).
  22. Brezezinski, & Marzec, M. The origin, dispersal and distribution of the American mink mustela vison in Poland. Acta Theriol (Warsz) 48, 505–514 (2003).
  23. Rȩk, Are changes in predatory species composition and breeding performance responsible for the decline of Coots fulica atra in Milicz Ponds reserve (SW poland)? Acta Ornithol 44, 45–52 (2009).
  24. Nieoczym, & Kloskowski, J. Habitat selection and reproductive success of coot Fulica atra on ponds under different fish size and density conditions. Hydrobiologia 820, 267–279 (2018).
  25. Halupka, , Czyż, B. & Macias Dominguez, C. M. The effect of climate change on laying dates, clutch size and productivity of Eurasian Coots Fulica atra. Int J Biometeorol 64, 1857–1863 (2020).
  26. Rönkä, T. H. et al. Environmental changes and population trends of breeding waterfowl in northern Baltic Sea. Annales Zoologici Fennici vol. 42 (2005).
  27. Stichting BirdLife Europe, BirdLife International & Article 12 EU population status assessments: Annex B – Bird species’ status and trends report format (Article 12) for the period 2013 – 2018. (2020).
  28. Walesiak, , Górecki, G. & Brzeziński, M. Recovery of Eurasian Coot Fulica atra and Great Crested Grebe Podiceps cristatus Breeding Populations in an Area Invaded by the American Mink Neovison vison. Acta Ornithol 54, 73 (2019).

Common Moorhen

Gallinula chloropus 2023-2028 Recommendation: research required.

Species trend

The UK breeding population of moorhen shows a substantial decline in breeding territories of 23 per cent. The wintering population, which includes migrants from much of Europe and North Africa, shows a ten-year decline of 26 per cent between 2008-2018. This is primarily driven by declines in England, as the Scottish and Welsh populations have shown slight increases over this period (four and five per cent respectively). The decline in Europe has not yet pushed the species into an ‘at risk’ category and the moorhen is currently listed as ‘of least concern’ on the European IUCN Red List. The decline of moorhens, like that of coots, is not well understood but, given the low bag size of the species, it is highly unlikely that shooting is the cause. Habitat loss and predation are suggested to be drivers, possibly impacting breeding success more than adult survival. Therefore, shooting restrictions are unlikely to have any benefit. Instead, research investment to better understand the causes of ongoing declines is necessary, alongside habitat management and conservation interventions.

Research required

  • Breeding and wintering surveys to better understand local and national distribution and abundance.
  • Submission of bag data to better inform harvest estimates (data can be submitted to the GWCT National Gamebag Census or BASC Green Shoots Bagged It).
  • Shooters should support the BASC wing survey to enable better understanding of adult: juvenile harvest ratios.
  • Increased ringing and ring resighting effort to improve understanding of migratory

Shooting restrictions

  • Should show
  • Site-based considerations

Habitat management

  • General wetland creation and management will benefit both breeding and wintering
  • A mosaic habitat of dense cover, open water and clearings is required to provide safe refuge and feeding areas.
  • Ensure suitable breeding sites have ramp-like areas to enable chicks to leave the water
  • Pest and predator
  • Refuge provision, either for set periods of time (temporal) or over dedicated areas of land (spatial), dependent on site requirements.
  • Nesting support (for example: fencing, duck nest tubes, provision of maintained islands).

Stage 2 assessment

Species summary

Moorhen are highly adaptive and flexible in their habitat use, now often associated with urban areas1,2. The decline of moorhen, like that of coot, is not well understood, but given the low game bag size of the species, it is highly unlikely that hunting is driving the species decline. Habitat loss and predation are suggested to be drivers of decline, possibly impacting breeding success more than adult survival3,4. Therefore wetland restoration, along with agricultural and artificial pond creation accompanied by re-vegetating and predator control, will likely benefit moorhen populations across their range.

Species conservation status (see Table 1)

The common moorhen population is showing declines across the UK and Europe. Data from the breeding population is only available for England (where the bulk of UK breeding moorhen are found) and shows a decline in breeding territories (-23.02%). The wintering population, which includes migrants from much of Europe and North Africa shows a 10-year decline (-26% between 2008/09-2018/19)5. This is primarily driven by declines in England, as the Scottish and Welsh populations have shown slight increases over this period (+4% and +5% respectively)6. The decline in Europe has not pushed the species into an ‘at risk’ category7.
BoCC8 (2020) IUCN UK8 (2020) Europe7 (2021) EU287 (2021) AEWA9 (2018) IUCN Global10 (Last updated in 2016)
Category A VU LC (B) LC (B) B2c LC
Trend (time period in brackets) Decreasing (Breeding & Wintering) Decreasing (over 3 generations) Decreasing (over 3 generations) Decreasing/ Stable (2009-2018) Stable
Population size estimate Mature individuals Breeding: 210 000 Territories5 Wintering: 305,000 Individuals11 1,790,000- 2,670,000 (min-max) 1,410,000- 1,970,000 (min-max) 2,600,000- 3,900,000 (min-max) 4,956,000- 8,400,000 (min-max)
Reason for category Moderate breeding pop. decline over longer term. Reduction in size of breeding pop (either abundance or range) of the population, measured over 3 generations. Declines of 20-30% over 3 generation lengths. n/a n/a Population >100,000 but is need of special attention as a result of long-term decline. Species has large range and population size. Trend is stable.

WeBS UK 10-year trend (2008/09-2018/19): -26%6 ● BBS UK 10-year trend (2010-2020): -20.63%5

Table 1. Species conservation status across different scales. *It has been highlighted by BASC that such automatic linkage between IUCN status and levels of protection by AEWA is directly contrary to the IUCN’s advice on the use of its list.

Population dynamics

Cooperative breeding and brood parasitism are both common in moorhens1,3,12. Due to moorhens high reproductive potential, they are also able to quickly colonise new habitat3. The species populations are prone to size fluctuations due their sensitivity to severe winter weather, however trends do suggest a downturn in population growth. Although moorhen are tolerant of human disturbance and readily occupy artificial waterbodies13–16, if the vegetation in these areas is heavily managed or there are high predation rates, it is likely that breeding success is impacted3,4. Further studies are required to understand the drivers of moorhen population dynamics.

Hunting and harvest

The moorhen shooting seasons in the UK are not compliant with the Key Concepts of Article 7(4)17. The start date of the open season in England and Wales (1st Sept) overlaps with the estimated end of the reproduction period for moorhen in the south of the UK by almost six ‘decades’ (approx. 1.5 months). This is therefore in breach of the agreement. Take of moorhen is already prohibited in Northern Ireland and the Isle of Man. There is no UK bag data available for moorhen. Similar to common coot, the species is rarely harvested and as a result there is no modern estimates of its harvest (nor the sustainability of this harvest). Harvest appears to be low in Europe but bag data is limited18. Harvest is also low across the remainder of the moorhens range, including in North America19, where there appears to be a low interest in hunting rails20,21. Moorhen show a preference for urban areas. Moorhen, like coot, are seen as synanthropic, i.e. they benefit from the artificial environments created by humans and broadly do well despite human disturbance13–16. There is no information about the impact of hunting on their behaviour and distribution.

Pressures, action and research

Pressures The modification or loss of small, vegetated ponds, particularly in agricultural areas is likely to have impacted moorhen across Europe22. In the presence of intense bankside and pond habitat management, moorhen will nest in trees1,3,4. However, if trees are absent from sites surrounding waterbodies, this may reduce survival and breeding success of moorhens. A limited number of cases of moorhen with avian influenza have been recorded. Moorhen found or inoculated with the virus did not show signs of illness but shed the virus quickly23. This suggests that the species could spread the virus easily to species that are more susceptible to infection and mortality23. Practical action Due to a limited understanding of the drivers of moorhen declines, clear practical actions cannot be recommended. However, creation and maintenance of ponds with stable water levels provide good breeding sites for moorhen22,24. These ponds require emergent vegetation and tall cover on surrounding land to provide suitable nesting sites2. Predator and pest control, particularly of rats and mink, will likely benefit the nesting success of moorhen3. Research action A large proportion of moorhen studies look at nesting behaviour, specifically cooperative breeding and nest parasitism1,3,12,25. However, there is limited understanding of the movement of moorhens within the UK and across the flyway. As with coot, this species would benefit from ringing or marking programmes that allow for capture-mark-recapture studies.

References

  1. Haraszthy, L. Intra-and interspecific nest parasitism of Common Moorhen (review of cases and new data). Ornis Hungarica 26 95–101 Preprint at https://doi.org/10.1515/orhu-2018-0007 (2018).
  2. Samraoui, , Alfarhan, A. H. & Samraoui, B. Status and breeding ecology of the Common Moorhen Gallinula chloropus in Algeria. Ostrich 84, 137–144 (2013).
  3. Forman, D. W., Brain, P. F. & Brain, P. F. Reproductive strategies used by moorhens (Gallinula chloropus) colonising an artificial wetland habitat in South Journal of Natural Histo… Article in Journal of Natural History https://www.researchgate.net/publication/262412829 (2004).
  4. Taylor, The influence of watercourse management on Moorhen breeding biology. British Birds 77, 144–148 (1984).
  5. Harris, S. J. et al. The Breeding Bird Survey 2021. BTO Research Report 745. bto.org (2022).
  6. Frost, T. M. et al. Waterbirds in the UK 2019/20: The Wetland Bird Survey. (2021).
  7. BirdLife European Red List of Birds. https://op.europa.eu/en/publications. (2021) doi:10.2779/967570.
  8. Stanbury, et al. The status of our bird populations: the fifth Birds of Conservation Concern in the United Kingdom, Channel Islands and Isle of Man and second IUCN Red List assessment of extinction risk for Great Britain. British Birds 114, 723–747 (2021).
  9. Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) – Agreement Text and Annexes As amended by MOP8. (2022).
  10. BirdLife Gallinula chloropus (amended version of 2016 assessment). The IUCN Red List of Threatened Species 2019. https://dx.doi.org/10.2305/IUCN.UK.2019-3.RLTS.T62120190A155506651.en (2019) doi:10.2305/IUCN.UK.2019-3.RLTS.T62120190A155506651.en.
  11. Woodward, et al. APEP 4: Population estimates of birds in Great Britain and the United Kingdom. British Birds 113, 69–104 (2020).
  12. Gibbons, W. Behavioral Ecology and Sociobiology Brood parasitism and cooperative nesting in the moorhen, GMlinula chloropus. Behav Ecol Sociobiol vol. 19 (1986).
  13. Adam, , Musilová, Z., Musil, P., Zouhar, J. & Romportl, D. Long-Term Changes in Habitat Selection of Wintering Waterbirds: High Importance of Cold Weather Refuge Sites. Acta Ornithol 50, 127–138 (2015).
  14. Talbi, , Samraoui, F., Samraoui, B., Zullo, F. & Battisti, C. Habitat selection of Coot (Fulica atra) and Moorhen (Gallinula chloropus) in a remnant Mediterranean wetland (Italy): Implications for conservation. Lakes Reserv 25, 413–418 (2020).
  15. Lai, C. H., Lin, S. H., Tsai, C. Y. & Chen, S. H. Identifying farm pond habitat suitability for the Common Moorhen (Gallinula chloropus): A conservation-perspective Sustainability (Switzerland) 10, (2018).
  16. Wang, , Ma, Y. fei & You, X. yi. An innovative approach to identify environmental variables with conservation priorities in habitat patches. J Environ Manage 292, (2021).
  17. Key concepts of Article 7(4) of Directive 79/409/EEC: Period of reproduction and prenuptial migration of Annex II bird species in the 28 Member States. (2014).
  18. Hirschfield, A. & Heyd, A. Mortality of migratory birds caused by hunting in Europe: bag statistics and proposals for the conservation of birds and animal Ber. Vogelschutz 42, 47–74 (2005).
  19. Case, J. & Sanders, S. J. Priority Information Needs for American Coots, Purple Gallinules and Common Moorhens: A Funding Strategy. https://digitalcommons.unl.edu/usfwspubs (2010).
  20. Eddleman, R., Knopf, F. L., Meanley, B., Reid, F. A. & Zembal~, R. Conservation of North American rallids. Wilson Bull 100, 458–475 (1988).
  21. Raftovich US Fish, v et al. Migratory Bird Hunting Activity and Harvest During the 2009 and 2010 Hunting Seasons. https://digitalcommons.unl.edu/usfwspubs (2011).
  22. Stichting BirdLife Europe, BirdLife International & Article 12 EU population status assessments: Annex B – Bird species’ status and trends report format (Article 12) for the period 2013 – 2018. (2020).
  23. Kang, et al. Pathogenicity and transmissibility of three avian influenza A (H5N6) viruses isolated from wild birds. Journal of Infection 76, 286–294 (2018).
  24. Dale, Population size and trend, and habitat selection of Common Moorhens (Gallinula chloropus) in Oslo and Akershus, southeastern Norway. Ornis Norv 44, 1–11 (2021).
  25. Mcrae, B. A Rise in Nest Predation Enhances the Frequency of Intraspecific Brood Parasitism in a Moorhen Population. Source: Journal of Animal Ecology vol. 66 (1997).

Golden Plover

Pluvialis apricaria

2023-2028 Recommendation: Current level of harvest and conservation effort to continue. No additional action required.

Research required

  • Monitoring the long-term impacts of afforestation in upland areas should be undertaken to understand long term impacts.
  • Historic bag returns and the submission of current bag data to better inform harvest estimates (data can be submitted to the Game & Wildlife Conservation Trust (GWCT) National Gamebag Census or BASC Green Shoots Bagged It).

Shooting restrictions

  • None

Habitat management

  • Moorland management targeted at red grouse and peatland restoration appears to benefit the species, particularly creation of habitat mosaics.
  • Creation of marshy areas in moorland encourages damp areas where plover chicks can feed.
  • Targeted predator control in areas where known breeding populations

Stage 2 assessment

Species summary

The conservation status of the species remains favourable across its range. Marginal declines in some populations are thought to be driven by habitat changes, particularly afforestation and loss of breeding habitat5-8. Climate change is also considered a major contributing factor to plover population trends in recent years9-11. Game bag numbers are small in the UK and there is no evident hunting-mediated driver of decline. Removal of the species from Schedule II may in fact result in a reduced incentive to undertake management that benefits this species.

Plover populations and trends within the UK and Europe are in a relatively stable position. However, with increasing impacts of climate change and continued agricultural change and afforestation, habitat changes are a threat to plover populations. Plover show broadly positive responses to moorland management for red grouse and agricultural management for all waders. Therefore, continued support and focus on restoration of breeding and foraging habitat in the uplands is important in retaining the species positive conservation status.

Species conservation status (see Table 1)

The European golden plover (herein plover) is a breeding resident in the UK whose population is boosted by over-wintering individuals from three different flyway populations (NW Europe, Iceland and UK/Denmark)1. The UK breeding population appears to be stable (+0.18% between 2010-2020), which is the result of declines in England (-20.48%) and increases in Scotland (+12.77%)2. The wintering population shows broad declines across all UK nations (-14% between 2008/09-2018/19), experienced most severely in Northern Ireland (-36%), followed by Wales (-19%), England (-12%) and Scotland (-10%)3. These declines are likely driven by population trends in migrant populations. Across the rest of its range, which stretches from eastern Europe and north Africa into Russia, the population is thought to be increasing, driving the overall positive global trend1,4.

Hunting and harvest

The plover shooting seasons in the UK are compliant with the Key Concepts of Article 7(4)16. Plover have fluctuating bag trends in the UK, however these are quite low overall and the species is not amongst the most popular quarry species (1,300 in 2004, 5,100 in 2012 and 870 in 2016)17. Given the population size in the UK, this small harvest is likely to be sustainable18.

However, population estimate for golden plover are considered unreliable, likely due to the large proportion of inland birds missed in WeBS counts19. There is also limited data available at the flyway-level hunting pressure on plover, however bag numbers historically have been highest in France20.

Plover are sensitive to disturbance and show changes in behaviour as a result of recreation activities such as walking6,21 and hunting22. Hunting disturbance led to an increased frequency of flight and time spent vigilant, reducing resting time22. This leads to increased energetic costs and may result in reduced body condition22. The impact of such disturbance appears to impact plover during and after the hunting activity22. Other recreational disturbance such as walking off designated paths causes disturbance among plovers and results in their avoidance of paths during the chick-rearing period6. If disturbance during brood-rearing is continuous this is thought to impact chick survival21.

 

BoCC12

(2020)

IUCN UK12

(2020)

Europe13

(2021)

EU2813

(2021)

AEWA14

(2018)

IUCN Global4

(Last updated

in 2016)

CategoryGLCLC (B)LC (B)C1LC
Trend (time period in brackets)

Breeding: Stable

(2010-2020)

Wintering: Decreasing

(2008/09-2018/19)

Stable (over 3 generations)Stable (over 3 generations)

UK: Decreasing NW Europe: Stable

Iceland: Decreasing

(2009-2018)

 

Increasing

Population size estimate Mature individuals

Breeding: 32,500-

50,500 Pairs

Wintering: 410,000

Individuals15

1,660,000-

2,310,000

(min-max)

415,000-

676,000

(min-max)

UK: 110,000-170,000

NW Europe:

1,200,000-2,100,000

(min-max)

Iceland: c. 1,200,000

1,260,000-

1,720,000

(min-max)

Reason for categoryn/an/an/an/aAll populations >100,000 and could significantly benefit from international cooperation but do not show declines, range contraction or data deficiency.Population has large range & size alongside an increasing trend.
WeBS UK 10-year trend (2008/09-2018/19): -14%3 ● BBS UK 10-year trend (2010-2020): +0.18%2

Table 1. Species conservation status across different scales. *It has been highlighted by BASC that such automatic linkage between IUCN status and levels of protection by AEWA is directly contrary to the IUCN’s advice on the use of its list.

Pressures, action and research

Pressures

Plover are primarily impacted by changes to habitat management or habitat loss.

Increase in afforestation negatively impacts plover densities, with lower densities near forest edges5-8. This is likely due to increased predator abundance, including martens, foxes, and crows5,7. As well as hydrological changes maturing woodland can have on surrounding habitat7. This is of particular concern with increasing afforestation programmes in upland areas5,7,10. Changes in agricultural and moorland management have negatively impacted plover abundance, including reduction in open pasture where plover forage, and reduction of heather burning and sheep grazing, both of which create short sward habitat for plover when well managed9,23. Development, particularly that of wind farms, has been shown to reduce the abundance of plover within close proximity to operational turbines11,24–26.

However, this was not shown to affect overall hatching and fledging success24,27. Climate

change is considered a major contributing factor to plover population trends in recent years9–11. Advance in plover laying dates, which is already occurring, is expected to continue and may result in reduced survival as chick hatching becomes mis-matched with food availability (primarily craneflies) 28. Milder winters will likely drive distribution changes29, and more severe winters will result in peaks in wintering numbers in the UK and Ireland as plover try to escape cold weather30.

Practical action

Plover generally show increases in response to moorland management targeted at red grouse or peatland restoration23,31–33. This includes creation of habitat mosaics comprising grass, rush and mixed age heather in moorland9. Grazing by sheep, at an appropriate pressure, or heather burning to create heterogeneous heather and grass habitat should also be a major part of moorland management prevent vegetation becoming too long and dense for breeding birds 9,23,33,34. However such habitat management should be accompanied by predator control9,33,35. Predator control, particularly that of foxes and crows, can enhance breeding success of plover almost three-fold32. Creation of marshy areas in moorland by blocking drainage ditches will encourage rushes and damp areas where plover chicks can feed9. This may mitigate against some of the impacts of climate change on cranefly, the primary prey of plover35,36. Environmental land management schemes should look to retain fields with high invertebrate abundances34. This may also include summer grazing to enable grass sward heights to be <5cm and management of ditches and drainage systems to prevent over-drainage of fields37. Forestry planning should consider buffer zones of >100’s of metres adjacent to planned woodland and the impact plantations may have on open-ground habitat used by birds7. Hunting-free reserves with appropriate habitat for foraging and resting will help to mitigate against the disturbance effects of hunting22. Recreational disturbance can also be reduced by ensuring there are defined access points and well-maintained routes for walkers6,21.

Research action

Better understanding of plover movement across the flyway, through ringing and reporting programmes would be beneficial10,38. Particularly given possible distribution shifts due to habitat and climate change38 and responses to severe cold weather10. Planning of windfarms should also continue to monitor the long-term impact of operational turbines on golden plover productivity. Afforestation programmes should also consider the edge-effects of forest creation on plover breeding grounds. The long-term impact of afforestation and potential changing dynamics as woodland matures should be monitored, especially with the increase afforestation programmes in upland areas5,7,10. Improved recording and reporting of bag statistics will also enable evaluation of harvest sustainability in Europe10.

References

  1. Wetlands International. Waterbird Populations Portal. wpp.wetlands.org (2022).
  2. Harris, S. J. et al. The Breeding Bird Survey 2021. BTO Research Report 745. bto.org (2022).
  3. Frost, T. M. et al. Waterbirds in the UK 2019/20: The Wetland Bird Survey. (2021).
  4. BirdLife Pluvialis apricaria. The IUCN Red List of Threatened Species 2016. https://dx.doi.org/10.2305/IUCN.UK.2016- (2016) doi:10.2305/IUCN.UK.2016.
  5. Amar, et al. Exploring the relationships between wader declines and current land-use in the British uplands. Bird Study 58, 13–26 (2011).
  6. Finney, K., Pearce-Higgins, J. W. & Yalden, D. W. The effect of recreational disturbance on an upland breeding bird, the golden plover Pluvialis apricaria. Biol Conserv 121, 53–63 (2005).
  7. Wilson, D. et al. Modelling edge effects of mature forest plantations on peatland waders informs landscape-scale conservation. Journal of Applied Ecology 51, 204–213 (2014).
  8. Hancock, J. M. H., Grant, M. C. & Wilson, J. D. Associations between distance to forest and spatial and temporal variation in abundance of key peatland breeding bird Bird Study 56, 53–64 (2009).
  9. Whittingham, J., Percival, S. M. & Brown, A. F. Habitat selection by golden plover Pluvialis apricaria chicks. Basic Appl. Ecol 2, 177–191 (2001).
  10. European Directorate-General for the Environment. European Union management plan 2009-2011 Golden plover (Pluvialis apricaria). (2009).
  11. Stichting BirdLife Europe, BirdLife International & Article 12 EU population status assessments: Annex B – Bird species’ status and trends report format (Article 12) for the period 2013 – 2018. (2020).
  12. Stanbury, et al. The status of our bird populations: the fifth Birds of Conservation Concern in the United Kingdom, Channel Islands and Isle of Man and second IUCN Red List assessment of extinction risk for Great Britain. British Birds 114, 723–747 (2021).
  13. BirdLife European Red List of Birds. https://op.europa.eu/en/publications. (2021) doi:10.2779/967570.
  14. Agreement on the Conservation of African-Eurasian Migratory Waterbirds (AEWA) – Agreement Text and Annexes As amended by MOP8. (2022).
  15. Woodward, et al. APEP 4: Population estimates of birds in Great Britain and the United Kingdom. British Birds 113, 69–104 (2020).
  16. Key concepts of Article 7(4) of Directive 79/409/EEC: Period of reproduction and prenuptial migration of Annex II bird species in the 28 Member States. (2014).
  17. Aebischer, N. J. Fifty-year trends in UK hunting bags of birds and mammals, and calibrated estimation of national bag size, using GWCT’s National Gamebag Eur J Wildl Res 65, (2019).
  18. Ellis, & Cameron, T. An initial assessment of the sustainability of waterbird harvest in the United Kingdom. bioRxiv (2022).
  19. Frost, et al. Population estimates of wintering waterbirds in Great Britain. British Birds vol. 112 (2019).
  20. Hirschfield, A. & Heyd, A. Mortality of migratory birds caused by hunting in Europe: bag statistics and proposals for the conservation of birds and animal Ber. Vogelschutz 42, 47–74 (2005).
  21. Pearce-Higgins, W., Finney, S. K., Yalden, D. W. & Langston, R. H. W. Testing the effects of recreational disturbance on two upland breeding waders. Ibis (2007).
  22. Casas, , Mougeot, F., Viñuela, J. & Bretagnolle, V. Effects of hunting on the behaviour and spatial distribution of farmland birds: Importance of hunting-free refuges in agricultural areas. Anim Conserv 12, 346–354 (2009).
  23. Douglas, J. T. et al. Changes in upland bird abundances show associations with moorland management. Bird Study 64, 242–254 (2017).
  24. Sansom, , Pearce-Higgins, J. W. & Douglas, D. J. T. Negative impact of wind energy development on a breeding shorebird assessed with a BACI study design. Ibis 158, 541–555 (2016).
  25. Pearce-Higgins, W., Stephen, L., Langston, R. H. W., Bainbridge, I. P. & Bullman, R. The distribution of breeding birds around upland wind farms. Journal of Applied Ecology 46, 1323–1331 (2009).
  26. Pearce-Higgins, W., Stephen, L., Langston, R. H. W. & Bright, J. A. Assessing the cumulative impacts of wind farms on peatland birds: a case study of golden plover Pluvialis apricaria in Scotland. vol.4 https://www.mires-and-peat.net/, (2008).
  27. Pearce-Higgins, J. W., Stephen, L., Douse, A. & Langston, R. H. W. Greater impacts of wind farms on bird populations during construction than subsequent operation: Results of a multi-site and multi-species analysis. Journal of Applied Ecology 49, 386–394 (2012).
  28. Pearce-Higgins, J. W., Yalden, D. W. & Whittingham, M. J. Warmer springs advance the breeding phenology of golden plovers Pluvialis apricaria and their prey (Tipulidae). Oecologia 143, 470–476 (2005).
  29. Gillings, , Austin, G. E., Fuller, R. J. & Sutherland, W. J. Distribution shifts in wintering Golden Plover Pluvialis apricaria and Lapwing Vanellus vanellus in Britain. Bird Study 53, 274–284 (2006).
  30. Machín, P. et al. Individual migration patterns of Eurasian golden plovers Pluvialis apricaria breeding in Swedish Lapland examples of cold spell-induced winter J Avian Biol 46, 634–642 (2015).
  31. Baines, D., Redpath, S., Richardson, M. & Thirgood, S. The direct and indirect effects of predation by Hen Harriers Circus cyaneus on trends in breeding birds on a Scottish grouse Ibis 150, 27–36 (2008).
  32. Fletcher, , Aebischer, N. J., Baines, D., Foster, R. & Hoodless, A. N. Changes in breeding success and abundance of ground-nesting moorland birds in relation to the experimental deployment of legal predator control. Journal of Applied Ecology 47, 263–272 (2010).
  33. Tharme, P., Green, R. E., Baines, D., Bainbridge, I. P. & O’Brien, M. The effect of management for red grouse shooting on the population density of breeding birds on heather-dominated moorland. Journal of Applied Ecology 38, 439–457 (2001).
  34. Whittingham, J., Percival, S. M. & Brown, A. F. Time budgets and foraging of breeding golden plover Pluvialis apricaria. Journal of Applied Ecology 37, 632–646 (2000).
  35. Pearce-Higgins, W. Modelling conservation management options for a southern range-margin population of Golden Plover Pluvialis apricaria vulnerable to climate change. Ibis 153, 345–356 (2011).
  36. Pearce-Higgins, J. W., Dennis, P., Whittingham, M. J. & Yalden, D. W. Impacts of climate on prey abundance account for fluctuations in a population of a northern wader at the southern edge of its range. Glob Chang Biol 16, 12–23 (2010).
  37. Pearce-Higgins, W. & Yalden, D. W. Variation in the use of pasture by breeding European Golden Plovers Pluvialis apricaria in relation to prey availability. Ibis 145, 365–381 (2003).
  38. Gillings, S. Plugging the gaps-winter studies of Eurasian Golden Plovers and Northern

Funding support

Financial support could be provided to fund research and practical conservation measures in the UK and abroad through an application for grant funding to the BASC Wildlife Fund.

Insurance

It is advisable to have adequate liability (third-party) insurance when shooting. Membership of BASC includes insurance for recreational sporting activities. Find out more and join BASC here.

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