Grey Partridge

Grey Partridge

Perdix perdix
Grey Partridge, Allan Drewitt

Introduction

The 'English' Partridge, as it is sometimes known, is a resident and sedentary bird, associated with lowland farmland.

Grey Partridges are best seen in winter, when the fields are bare and the birds gather in small groups called 'coveys' to feed on seeds, roots and shoots. Their bodies form small mounds which can be mistaken for clods of earth, or even for Brown Hares which often share the same habitat.

Once widespread, the Grey Partridge is now Red-listed as a Bird of Conservation Concern in the UK due to steep population declines, which have been linked to agricultural intensification.

  • Our Trends Explorer gives you the latest insight into how this species' population is changing.
Grey Partridge, Allan Drewitt

Key Stats

Status
Common
Common
Eggs
Eggs
13-16
BTO Records
BTO Records
120k records
Population and distribution stats for:
Population Change
Population Change
92% decrease 1967–2022
Population Size
Population Size
37k Territories
Distribution Change
Distribution_change
-40.8% contraction
Population Size
Population Size
No current data
Distribution Change
Distribution_change
-22.8% contraction

Identification

Curated resources to aid in the identification of Grey Partridge

ID Videos

This section features BTO training videos headlining this species, or featuring it as a potential confusion species.

Partridges

Songs and Calls

Listen to example recordings of the main vocalisations of Grey Partridge, provided by xeno-canto contributors.

Song:

Call:

Movement

Information about Grey Partridge movements and migration based on online bird portals (e.g. BirdTrack), Ringing schemes and tracking studies.

Britain & Ireland movement

View a summary of recoveries in the Online Ringing Report

Foreign locations of birds ringed or recovered in Britain & Ireland

Dots show the foreign destinations of birds ringed in Britain & Ireland, and the origins of birds ringed overseas that were subsequently recaptured, resighted or found dead in Britain & Ireland. Dot colours indicate the time of year that the species was present at the location.

  • Winter (Nov-Feb)
  • Spring (Mar-Apr)
  • Summer (May-Jul)
  • Autumn (Aug-Oct)
Foreign locations of birds ringed or recovered in Britain & Ireland

European movements

EuroBirdPortal uses birdwatcher's records, such as those logged in BirdTrack to map the flows of birds as they arrive and depart Europe. See maps for this species here.

Biology

Lifecycle and body size information for Grey Partridge, including statistics on nesting, eggs and lifespan based on BTO ringing and nest recording data.

Productivity and Nesting

Nesting timing

Typical (exceptional) number of broods
1

Egg measurements

Typical length x width
36x27 mm
Mass (% shell)
14.1g (10%)

Clutch Size

Typical number
16-13 eggs
Observed minimum and maximum
4-29 eggs

Incubation

Incubation by
Female
Typical duration
25-23 days

Fledging

Type of chick
Precocial, downy
Typical duration
16-14 days
Visit our Trends Explorer for trend graphs and country statistics.

Survival and Longevity

Survival is shown as the proportion of birds surviving from one year to the next and is derived from bird ringing data. It can also be used to estimate how long birds typically live.

View number ringed each year in the Online Ringing Report.

lifespan

Typical life expectancy of bird reaching breeding age
3 years with breeding typically at 1 year
Maximum age from a ringed bird
5 years, 2 months, 13 days (set in 1978)

Survival of adults

All adults
0.55

Survival of juveniles

All juveniles
0.22
Visit our Trends Explorer for trend graphs and country statistics.

Biometrics

Wing length and body weights are from live birds (source).

Wing length

Average ±1 std deviation; range and sample size in brackets.
All adults
161.3±4.5 mm
(155-170 mm, N=29)
Visit our Trends Explorer for trend graphs and country statistics.

Ring Size

E*

Classification, names and codes

Taxonomy, names and species codes for Grey Partridge

Classification and Codes

  • Order: Galliformes
  • Family: Phasianidae
  • Scientific name: Perdix perdix
  • Authority: Linnaeus, 1758
  • BTO 2-letter code: P.
  • BTO 5-letter code: GREPA
  • Euring code number: 3670

Alternate species names

  • Catalan: perdiu xerra
  • Czech: koroptev polní
  • Danish: Agerhøne
  • Dutch: Patrijs
  • Estonian: nurmkana
  • Finnish: peltopyy
  • French: Perdrix grise
  • Gaelic: Cearc-thomain
  • German: Rebhuhn
  • Hungarian: fogoly
  • Icelandic: Akurhæna
  • Irish: Patraisc
  • Italian: Starna
  • Latvian: laukirbe
  • Lithuanian: pilkoji kurapka
  • Norwegian: Rapphøne
  • Polish: kuropatwa (zwyczajna)
  • Portuguese: charrela
  • Slovak: jarabica polná
  • Slovenian: jerebica
  • Spanish: Perdiz pardilla
  • Swedish: rapphöna
  • Welsh: Petrisen
  • English folkname(s): English Partridge

Research

Interpretation and scientific publications about Grey Partridge from BTO scientists.

Causes of Change and Solutions

Causes of change

The ultimate factor behind the decline is the deterioration of the bird's agricultural habitat. There is convincing evidence showing that a steep drop in chick survival rate as a result of decreasing chick food availability due to agricultural intensification is the primary driver of population declines. A reduction of hen survival rate during incubation, lower nest success and reduction of winter survival, related to increased predation rates, have all been reported as also playing secondary roles.

Further information on causes of change

Modelling suggests that climate change may have had a positive impact on the long-term trend for this species, resulting in less negative trends than would have occurred in the absence of climate change (Pearce-Higgins & Crick 2019). However, any such positive effect has clearly been minimal in comparison to the negative drivers of change.

The ultimate factor behind the decline of this species is the deterioration of the bird's agricultural habitat (Aebischer & Ewald 2004). A detailed field and modelling study in the 1980s provides excellent evidence relating to the ecology and population dynamics of the Grey Partridge in a large (62 sq km) study area in Sussex (Potts 1980, Potts 2012). Potts (1980, 2012) identified a reduction in chick survival during the first six weeks after hatching due to a herbicide-induced fall in cereal invertebrate abundance as the primary reason for the decline. More recently, the intensive use of broad-spectrum insecticides on cereals in the summer has been associated with a further reduction in average chick survival rate (Aebischer & Potts 1998). A field study involving an experimental set-up using sprayed and non-sprayed fields confirmed that invertebrate food supplies were important as it was shown that use of pesticides reduced food available to chicks, resulting in lower chick survival and thus depleting numbers of birds being recruited into the population (Rands 1985). Further support for this comes from Sotherton et al. (1993), who also both found that chick survival rate was lower in sprayed than in unsprayed areas. A tracking study found that breeding birds preferred unimproved rough grazing habitat on hill farms in north-east England. This habitat provided tall rushes as nesting cover and invertebrate food for chicks, especially sawfly larvae (Warren et al. 2017)

Potts also identified two other causes for the decline: the disappearance of nesting cover as field boundaries were removed to improve farming efficiency and lower brood production resulting from increased predation. There is evidence from various sources indicating that a reduction of hen survival rate during incubation, lower nest success and a reduction of winter survival, related to increased predation rates, have been influential in the continued population decrease from the 1970s (Potts & Aebischer 1995, Tapper et al. 1996, Bro et al. 2000, De Leo et al. 2004, Panek 2005).

Aebischer & Ewald (2010) offer convincing evidence that, since 2002, local Grey Partridge recoveries have been made possible by sympathetic management of rotational set-aside to provide cover for chicks. In an area of nearly 1,000 ha in Hertfordshire, set-aside was used for habitat creation and Grey Partridge breeding density increased sixfold. However, the disappearance of rotational set-aside in 2007, which halved the amount of brood-rearing habitat, with concurrent poor weather, reversed the increase and effectively removed this potential mechanism for national population recovery.

Overshooting due to the failure of hunters to separate Grey Partridges from Red-legs can have local population effects, but this is not likely to be a national problem (Aebischer & Ewald 2004). Aebischer & Ewald (2010) showed that on Partridge Count Scheme (PCS) sites, the annual change in spring density in recent years was not related to either shooting pressure or intensity of Red-legged Partridge releasing and suggest that provision of brood-rearing habitats and game cover increased with the latter, which probably counteracted the shooting losses of Grey Partridges on Red-legged Partridge shoots.

In some areas, parasite-mediated apparent competition with the Pheasant may be influencing the decline and subsequent recovery of wild Grey Partridges (Tompkins et al. 2000a, b). However, the evidence for this is conflicting, as Sage et al. (2002) found no deleterious fitness effects of the parasite and Browne et al. (2006) found that poor wild brood survival was indicative of low habitat and food quality rather than of a high rate of parasite infection. There is also evidence from a French study that Red-legged Partridges are dominant to Grey Partridges where they co-occur (Rinaud et al. 2020); however, there is no evidence yet to indicate that this may also be true in the UK and hence may have contributed to the UK declines.

Information about conservation actions

This species is well-studied and the conservation requirements are therefore fairly well understood. Research has shown that agricultural intensification is the main driver of declines and that, at a local level, the provision of nesting habitat and the reduction of pesticide-use can help increase productivity by increasing chick survival rates; hence actions such as the provision of conservation headlands, uncultivated margins, buffer strips and rotational set-aside, the sowing of wild bird seed mixtures to increase the proportion of natural or semi-natural vegetation, and reducing the area sprayed with herbicides will help improve and increase habitat for partridges (see Causes of Change section, above). Predator control may also help increase local populations (Tapper et al. 1996). Where this species occurs at Red-legged Partridge hunts, appropriate measures should be put in place to ensure accidental shooting of Grey Partridges is minimised and hence does not impact on local populations of the native species, as described by Aebischer & Ewald ( 2010).

Whilst such actions may help increase Grey Partridge numbers on individual farms (Aebischer & Ewald 2004; Newton 2004; Aebischer & Ewald 2010; Aebischer & Ewald 2010; Ewald et al. 2010), policies to encourage wider take up of the conservation actions described above may be needed in order to enable national populations to recover. Hence the inclusion of specific options in agri-environment schemes and payments to farmers for their provision may be required.

More Evidence

More evidence from Conservation Evidence.com

Partners

Birdfacts is based on data collected by volunteers participating in surveys that are organised and funded by BTO, RSPB, Esmée Fairbairn Foundation, JNCC and other partners.
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