Great Tit

Great Tit

Parus major
Great Tit, Liz Cutting

Introduction

The Great Tit is a common visitor to garden bird feeders. Outside urban areas, it is primarily a species of scrub and deciduous woodland.

The Great Tit is a striking little bird, with a bluish-green back and a yellow breast divided by a central black stripe. The sexes are similar, but in males the black stripe is more pronounced. It is a vocal species with a huge range of songs and calls; its most familiar is its repeated 'teacher-teacher-teacher' song which can be heard throughout woodlands in spring.

UK Great Tit numbers increased from the 1960s, although they have stablised since about 2010. Great Tits take readily to nest boxes, and lay one (sometimes two) clutches a year. They are primarily insectivorous in summer, but over winter they frequent bird feeders and are often found in mixed flocks with other tit species. They are widespread throughout Britain & Ireland apart from on some islands in northern and western Scotland.

  • Our Trends Explorer gives you the latest insight into how this species' population is changing.
Great Tit, Liz Cutting

Key Stats

Status
Common
Common
Weight
Weight
18.6g
Eggs
Eggs
7-9
BTO Records
BTO Records
9.5m records
Population and distribution stats for:
Population Change
Population Change
77% increase 1967 to 2023
Population Size
Population Size
2m territories
Distribution Change
Distribution_change
3.7% expansion

Identification

Curated resources to aid in the identification of Great Tit

ID Videos

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

GBW: Blue Tit and Great Tit

#BirdSongBasics: Great Tit and Coal Tit

#BirdSongBasics: Blue Tit and Great Tit

Songs and Calls

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

Song:

Call:

Begging call:

Movement

Information about Great Tit 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.

The Eurasian-African Migration Atlas shows movements of individual birds ringed or recovered in Europe. See maps for this species here.

Biology

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

Productivity and Nesting

Nesting timing

Average (range) fo first clutch laying dates
26 Apr (10 Apr-17 May)
Typical (exceptional) number of broods
1(2)

Egg measurements

Typical length x width
18x14 mm
Mass (% shell)
1.7g (6%)

Clutch Size

Typical number
7-9 eggs
Average ±1 standard deviation
7.94±1.86 eggs
Observed minimum and maximum
2-16 eggs

Incubation

Incubation by
Female
Typical duration
13-14 days
Observed average ±1 standard deviation
13.85±1.29 days
Observed minimum and maximum
12-16 days

Fledging

Type of chick
Altricial, downy
Typical duration
18-21 days
Observed average ±1 standard deviation
18.06±1.96 days
Minimum and maximum
15-21.5 days
N=5175, -Source
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
10 years, 5 months, 18 days (set in 2006)

Survival of adults

All adults
0.542±0.011
Females
0.555±0.034
Males
0.583±0.028

Survival of juveniles

All juveniles
0.38±0.014 (in first year)
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.
Juvenile
74.5±2.1 mm
(71-78 mm, N=34300)
All adults
75±3.8 mm
(71-79 mm, N=53986)
Female
73.5±1.8 mm
(71-76 mm, N=26096)
Male
76.5±4.7 mm
(73-79 mm, N=27388)

Body weight

Average ±1 std deviation; 5th and 95th percentiles and sample size in brackets.
Juvenile
18.6±3.1 g
(16.6-20.6 g, N=27373)
All adults
18.6±2.8 g
(16.6-20.8 g, N=42606)
Female
18.1±2 g
(16.3-20.2 g, N=20699)
Male
19.1±3.3 g
(17.3-21 g, N=21527)
Visit our Trends Explorer for trend graphs and country statistics.

Ring Size

A or B (pulli B)

Classification, names and codes

Taxonomy, names and species codes for Great Tit

Classification and Codes

  • Order: Passeriformes
  • Family: Paridae
  • Scientific name: Parus major
  • Authority: Linnaeus, 1758
  • BTO 2-letter code: GT
  • BTO 5-letter code: GRETI
  • Euring code number: 14640

Alternate species names

  • Catalan: mallerenga carbonera
  • Czech: sýkora konadra
  • Danish: Musvit
  • Dutch: Koolmees
  • Estonian: rasvatihane
  • Finnish: talitiainen
  • French: Mésange charbonnière
  • Gaelic: Currac-baintighearna
  • German: Kohlmeise
  • Hungarian: széncinege
  • Icelandic: Flotmeisa
  • Irish: Meantán Mór
  • Italian: Cinciallegra
  • Latvian: liela zilite
  • Lithuanian: didžioji zyle
  • Norwegian: Kjøttmeis
  • Polish: bogatka (zwyczajna)
  • Portuguese: chapim-real
  • Slovak: sýkorka velká
  • Slovenian: velika sinica
  • Spanish: Carbonero común
  • Swedish: talgoxe
  • Welsh: Titw Mawr
  • English folkname(s): Titmouse

Research

Interpretation and scientific publications about Great Tit from BTO scientists.

Causes of Change and Solutions

Causes of change

Demographic trends in breeding parameters do not suggest that increases in this species are due to improvements in breeding performance. There is some evidence, albeit limited, that improvements in survival rates, due to amelioration in wintering conditions, may have been responsible. Evidence for ecological drivers of the population increase is limited but increased provisioning in gardens and milder winters may have played a role.

Further information on causes of change

The number of fledglings per breeding attempt have decreased alongside decreases in clutch and brood sizes (see above). Daily failure rates at the egg stage have also decreased but daily failure rates at the chick stage has not changed. Consequently, breeding success does not contribute substantially to population change, and integrated modelling confirms that variation in adult survival is the primary driver of annual population change (Robinson et al. 2014).

Increases in survival rates, due to more widespread food provision in gardens during winter is one possible explanation for the increase (Plummer et al. 2019). Horak & Lebreton (1998) found that survival rates in Estonia were higher in urban populations than rural ones and suggested that this was partly due to supplementary feeding in gardens. Increasing winter temperature may have also played a role. Ahola et al. (2009) suggested that, for their study population in Sweden, increasingly favourable conditions in winters have enhanced the survival rates of Great Tit and resulted in the observed increase in Great Tit breeding density.

Other factors are also likely to influence survival rates. There is some evidence that the beech crop may be influential and it has been shown that survival rates can be related to beechmast production (Verhulst 1992, Perdeck et al. 2000), although there is no evidence that beechmast production has gone up. Perdeck et al. (2000) provided further evidence for this as supplemental food increased survival of both juveniles and adults, supporting the winter-food limitation hypothesis. In a Finnish population, Orell (1989) reported that the high survival rates of resident juveniles after a warm August may be attributable to food availability during the time when the birds undergo their post-juvenile moult.

Great Tits have advanced their laying date, in line with climatic change. This has been found by several studies (e.g. Sanz 2002, Visser et al. 2009, Bauer et al. 2010), but does not seem to be influencing the population trend. Intraspecific competition may also drive population changes in Great tits (Gamelon et al. 2019), and there is evidence that density-dependent effects influence clutch size, hatching success and fledging success, which may explain the decreases observed in clutch size as fledging rates as the population has increased (Bodey et al. 2020). Severe weather events are expected to become more frequent as a result of climate change and conditions such as heavy and persistent rainfall can also be an important driver of Great Tit breeding success (Scholl et al. 2020); however, there is no evidence that this has driven population change.

Information about conservation actions

Like its close relative the Blue Tit, the population of this species has increased since the 1970s, hence it is not a species of concern and no conservation actions are currently required. However, it has experienced a shallow decline over the last ten years and therefore ongoing monitoring would be prudent.

Ongoing provision of garden bird food is likely to continue to benefit the Great Tit. However, the effects are not always entirely positive and feeders may contribute to the spread of avian pox, so those providing food should ensure they follow good hygiene practices. The provision of nest boxes, both in gardens and elsewhere, is also likely to continue to benefit this species.

Publications (8)

Temporal avoidance as a means of reducing competition between sympatric species

Author: Maziarz, M., Broughton, R.K., Beck, K.B., Robinson, R.A. & Sheldon, B.C.

Published: 2023

Human activities modify the availability of natural resources for other species, including birds, and may alter the relationships between them. The provision of supplementary food at garden feeding stations, for example, might favour some species over others and change the competitive balance between them. This paper investigates the behavioural responses to competition of the Marsh Tit, a species that is subordinate to both the Blue Tit and the Great Tit.

24.05.23

Papers

View on journal website

A review of the impacts of air pollution on terrestrial birds

Author: Barton, M.G., Henderson, I., Border, J.A. & Siriwardena, G.M.

Published: 2023

A review paper by BTO considers 203 studies of the effects of air pollution on 231 bird species. Of these studies, 82% document at least one negative effect associated with increasing levels of pollution. The review also highlights biases towards particular study species, especially Great Tit and Pied Flycatcher, and also towards particular geographical regions (Western Europe) and pollutants (heavy metals). The paper proposes research approaches that could help to provide a fuller understanding of how birds are impacted by air pollution.

15.05.23

Papers

View on journal website

Evidence that rural wintering populations supplement suburban breeding populations

Author: Hanmer, H.J., Dadam, D. & Siriwardena, G.M.

Published: 2022

Urban areas can and do hold significant populations of birds, but we know surprisingly little about how these populations are connected with those present within the wider countryside. It has been suggested that the populations using these different habitats may be linked through seasonal movements, with individuals breeding in rural areas moving into urban sites during the winter months to exploit the supplementary food provided at garden feeding stations. However, little work has been done to test this hypothesis.

24.11.22

Papers Bird Study

View this paper online

The effects of a decade of agri-environment intervention in a lowland farm landscape on population trends of birds and butterflies

Author: Redhead, J.W., Hinsley, S.A., Botham, M.S., Broughton, R.K., Freeman, S.N., Bellamy, P.E., Siriwardena, G., Randle, Z., Nowakowski, M., Heard, M.S. & Pywell, R.F.

Published: 2022

Food production and wildlife conservation are often thought of as incompatible goals, and it is rare that conservation studies consider both economics and long-term changes in ecology. However, a decade-long study at a commercial arable farm in Buckinghamshire has found that agri-environment schemes significantly increased local bird and butterfly populations without damaging food production, offering hope for the UK’s farmland birds and butterflies.

01.08.22

Papers

Tritrophic phenological match-mismatch in space and time

Author: Burgess M.D., Smith K.W., Evans K.L., Leech D., Pearce-Higgins J.W., Branston C.J., Briggs K., Clark J.R., du Feu C.R., Lewthwaite K., Nager R.G., Sheldon B.C., Smith J.A., Whytock R.C., Willis S.G., Phillimore A.B.

Published: Spring 2018

The increasing temperatures associated with a changing climate may disrupt ecological systems, including by affecting the timing of key events. If events within different trophic levels are affected in different ways then this can lead to what is known as phenological mismatch. But what is the evidence for trophic mismatch, and are there spatial or temporal patterns within the UK that might point to mismatch as a driver of regional declines in key insect-eating birds? A changing climate is leading to changes in the timing of key ecological events, including the timing of bud burst, the spring peak in leaf-eating caterpillar biomass and the timing of egg-laying in many bird species. If the timings of these different events shift at different rates then there is a danger that they may get out of synch with one another, something that is referred to as phenological mismatch. This may be a particular problem for birds like Blue Tit, Great Tit and Pied Flycatcher, which time their breeding attempts to exploit the spring peak in caterpillar abundance. Much of the recent work on mismatch and its impacts on the fitness and population trends of caterpillar-eating birds has looked at changes over time. However, it is also possible for mismatch to vary in space if species respond differently in different areas, perhaps because of local adaptation to geographic variation in the cues that they use. This paper looks at mismatch in both space and time, using information from three trophic levels, namely trees, caterpillars and caterpillar-eating birds. While information on bud burst came from 10,000 observations of oak first leafing for the period 1998-2016, that for caterpillar biomass was inferred from frass traps set beneath oak trees at sites across the UK for the period 2008-2016. Bird phenology data came from the ‘first egg date’ values calculated from 85,000 nest records of Blue Tit, Great Tit and Pied Flycatcher. The focus of the work was on the relationship between the phenologies of these interacting species; where timing changes more in one species than the other, this is indicative of spatial or temporal variation in the magnitude of mismatch. The results reveal that, for the average latitude (52.63°N) and year, there is a 27.6 day interval between the timing of oak first leaf and peak caterpillar biomass. With increasing latitude, the delay in oak leafing is significantly steeper than that of the caterpillar peak. At 56°N the predicted interval between these two trophic levels drops to 22 days. In the average year and at the average latitude, the first egg dates of Blue Tits and Great Tits were roughly a month earlier than peak caterpillar biomass, meaning that peak demand for hungry chicks occurred soon after the peak in resource availability. Interestingly, peak demand in Pied Flycatchers occurred nearly two weeks later than peak caterpillar availability, suggesting a substantial trophic mismatch between demand and availability for this species within the UK. However, it is worth noting that Pied Flycatchers provision their nestlings with fewer caterpillars and more winged invertebrates compared to the tit species studied, so they may be less dependent on the caterpillar peaks. The work also revealed that the timing of first egg date between years varied by less than the variation seen in timing of the caterpillar resource peak, which gave rise to year-to-year variation in the degree of mismatch. For every 10 day advance in the caterpillar peak, the corresponding advance in the three bird species is 5.0 days (Blue Tit), 5.3 days (Great Tit) and 3.4 days (Pied Flycatcher). In late springs, peak demand from the tits is expected to coincide with the peak resource availability, with flycatcher demand occurring shortly after. In early springs, the peak demand of nestlings of all three species falls substantially later than the peak, leaving the three mismatched. Warmer conditions also shortened the duration of caterpillar peaks. One of the key findings of the work is that in the average year there is little latitudinal variation in the degree of caterpillar-bird mismatch. This means that more negative declines in population trends of certain insectivorous birds in the southern UK, driven by productivity, are unlikely to have been driven by greater mismatch in the south than the north. The lack of evidence for latitudinal variation in mismatch between these bird species and their caterpillar prey suggests that mismatch is unlikely to be the driver of the spatially varying population trends found in these and related species within the UK.

23.04.18

Papers

Health hazards to wild birds and risk factors associated with anthropogenic food provisioning

Author: Lawson, B., Robinson, R. A., Toms, M. P., Risely, R., MacDonald, S., Cunningham, A. A.

Published: 2018

Work on emerging infectious diseases and garden birds in the UK has been supported by citizen science projects, most notably Garden BirdWatch, Garden Wildlife Health and the Garden Bird Health Initiative – the latter now superseded by Garden Wildlife Health. Through these schemes, researchers have been able to carry out national surveillance of emerging diseases, including finch trichomonosis, Paridae pox and passerine salmonellosis. This paper, part of a special issue of Philosophical Transactions focusing on wildlife disease issues, reviews the work that has been carried out on these diseases over the past 25 years. It also takes a look at the occurrence of mycotoxin contamination of food residues in bird feeders, which also pose a risk to the health of wild birds. A citizen science approach provides a cost-effective means to undertake large-scale and year-round disease surveillance (Garden Wildlife Health), delivered in parallel to the monitoring of wildlife populations (Garden BirdWatch). By combining large-scale surveillance and targeted post-mortem examinations we can differentiate between the multiple diseases that result in non-specific clinical signs (e.g. lethargy and a fluffed-up appearance). The sample archive collected through post-mortem examination also enables future identification of other disease agents, including those – such as environmental pollutants – associated with non-infectious disease. Avian trichomonosis, caused by the protozoan parasite Trichomonas gallinae, has long been known to affect pigeons, doves and birds of prey. Its emergence in finches in 2005 led to a major population decline in Greenfinch and Chaffinch, reported in an earlier paper. While multiple strains of Trichomonas gallinae are known to infect pigeons and doves in the UK, a single clonal strain is responsible for the epidemic seen in finches. Quite why Greenfinch is so susceptible to the disease is unclear. It is likely that the disease spilled over into finches following the increase in use of garden feeding stations by Woodpigeon, a recent change that follows an increase in wider countryside populations. Avian poxvirus has been documented in a number of garden bird species and is most often seen in House Sparrow, Starling, Woodpigeon and Dunnock. Its emergence in UK tits saw a more severe form of the disease, resulting in pronounced skin lesions, some of which were likely to have hampered the individual’s ability to feed and to avoid predators. Sequence analysis of the poxvirus strains affecting garden birds revealed that a single clade is responsible for the disease seen in UK tits. This form has been known in Scandinavia since the 1950s, with incidents seen elsewhere in mainland Europe since 2005. Because UK tits are relatively sedentary in their habits, and because of the geographical pattern of disease spread seen, it is likely that the disease reached the UK via a biting insect – such as a mosquito, crossing the English Channel in a warm plume of air. Salmonellosis has been reported in wild birds since at least the 1950s, with the bacterium responsible known to be capable of persisting in the environment for many months. Greenfinch and House Sparrow are the two species in which the disease is most often seen. Passerine salmonellosis incidents have a clear seasonality, peaking in January. Interestingly, the prevalence of the disease in UK passerines has dropped sharply over recent years. This may reflect increased immunity to the particular form (DT56v) that had been seen here; or it may be that transmission is density-dependent, with the sharp decline in Greenfinch populations resulting in much lower rates of transmission. Mycotoxins, which include the aflatoxins and ochratoxin, are secondary metabolites produced by certain fungi of the genera Aspergillus and Penicillium. Exposure to the aflatoxins and ochratoxin can exert a range of adverse effects in birds, and the fungi involved and their toxins are known to occur on foodstuffs, including peanuts. Food residues from bird feeders were screened for the toxins as part of the current study, with detectable aflatoxin residues found in all seven samples, two of which greatly exceeded the maximum permitted limits set for such residues in peanuts destined for livestock feed, which includes wild bird food. It therefore seems likely that garden birds may be exposed to these toxins at levels associated with toxic effects in captive birds. This review underlines the great deal of new information that has been generated through these citizen science projects. It also highlights future research needs, particularly around the identification of risk factors, and that we need to understand the balance of risks and opportunities that garden bird feeding provides.

12.03.18

Papers

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