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The human population is increasingly disconnected from nature due to urbanisation. To counteract this phenomenon, the UK government has been actively promoting wildlife gardening. However, the extent to which such activities are conducted and the level of resource provision for biodiversity (e.g., food and nesting sites) within domestic gardens remains poorly documented. Here we generate estimates for a selection of key resources provided within gardens at a national scale, using 12 survey datasets gathered across the UK. We estimate that 22.7 million households (87% of homes) have access to a garden. Average garden size is 190 m2, extrapolating to a total area of 432,924 ha. Although substantial, this coverage is still an order of magnitude less than that of statutory protected areas. Approximately 12.6 million (48%) households provide supplementary food for birds, 7.4 million of which specifically use bird feeders. Similarly, there are a minimum of 4.7 million nest boxes within gardens. These figures equate to one bird feeder for every nine potentially feeder-using birds in the UK, and at least one nest box for every six breeding pairs of cavity nesting birds. Gardens also contain 2.5–3.5 million ponds and 28.7 million trees, which is just under a quarter of all trees occurring outside woodlands. Ongoing urbanisation, characterised by increased housing densities, is inevitable throughout the UK and elsewhere. The important contribution domestic gardens make to the green space infrastructure in residential areas must be acknowledged, as their reduction will impact biodiversity conservation, ecosystem services, and the well-being of the human population.
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A national scale inventory of resource provision for
biodiversity within domestic gardens
Zoe G. Davies
a
, Richard A. Fuller
a,1
, Alison Loram
a,2
, Katherine N. Irvine
b
,
Victoria Sims
a,3
, Kevin J. Gaston
a,*
a
Biodiversity and Macroecology Group, Department of Animal and Plant Sciences, University of Sheffield, Sheffield S10 2TN, UK
b
Institute of Energy and Sustainable Development, De Montfort University, The Gateway, Leicester LE1 9BH, UK
ARTICLE INFO
Article history:
Received 3 September 2008
Received in revised form
2 December 2008
Accepted 6 December 2008
Keywords:
Backland development
Backyard
Biodiversity
Conservation
Green space
Urban planning
ABSTRACT
The human population is increasingly disconnected from nature due to urbanisation. To
counteract this phenomenon, the UK government has been actively promoting wildlife gar-
dening. However, the extent to which such activities are conducted and the level of
resource provision for biodiversity (e.g., food and nesting sites) within domestic gardens
remains poorly documented. Here we generate estimates for a selection of key resources
provided within gardens at a national scale, using 12 survey datasets gathered across the
UK. We estimate that 22.7 million households (87% of homes) haveaccess to a garden. Aver-
age garden size is 190 m
2
, extrapolating to a total area of 432,924 ha. Although substantial,
this coverage is still an order of magnitude less than that of statutory protected areas.
Approximately 12.6 million (48%) households provide supplementary food for birds, 7.4
million of which specifically use bird feeders. Similarly, there are a minimum of 4.7 million
nest boxes within gardens. These figures equate to one bird feeder for every nine poten-
tially feeder-using birds in the UK, and at least one nest box for every six breeding pairs
of cavity nesting birds. Gardens also contain 2.5–3.5 million ponds and 28.7 million trees,
which is just under a quarter of all trees occurring outside woodlands. Ongoing urbanisa-
tion, characterised by increased housing densities, is inevitable throughout the UK and
elsewhere. The important contribution domestic gardens make to the green space infra-
structure in residential areas must be acknowledged, as their reduction will impact biodi-
versity conservation, ecosystem services, and the well-being of the human population.
2008 Elsevier Ltd. All rights reserved.
1. Introduction
For the first time in recorded history, over half of the global
human population live in urban areas and are, therefore,
becoming progressively disconnected from the natural world
(Wilson, 1984; Pyle, 2003; Miller, 2005). In developed countries
this proportion is much higher and, on average, is expected to
rise to 84% by 2030 (United Nations, 2007). In fact, urban areas
are presently expanding at a faster rate than any other land
use type (Meyer and Turner, 1992; McKinney, 2002), with
approximately 4% of global land cover being defined as urban-
ised (characterised by high human population densities or
0006-3207/$ - see front matter 2008 Elsevier Ltd. All rights reserved.
doi:10.1016/j.biocon.2008.12.016
*Corresponding author: Tel.: +44 (0)114 2220030; fax: +44 (0)114 2220002.
E-mail addresses: z.davies@sheffield.ac.uk (Z.G. Davies), r.fuller@uq.edu.au (R.A. Fuller), Alison.loram@basc.org.uk (A. Loram),
kirvine@dmu.ac.uk (K.N. Irvine), victoria.sims@atmosconsulting.com (V. Sims), k.j.gaston@sheffield.ac.uk (K.J. Gaston).
1
Present address: Spatial Ecology Lab, The Ecology Centre, The University of Queensland, St. Lucia, QLD 4072, Australia.
2
Present address: The British Association for Shooting and Conservation, Marford Mill, Rossett, Wrexham LL12 0HL, UK.
3
Present address: Atmos Consulting Ltd., Waen Farm, Nercwys Road, Mold, UK.
BIOLOGICAL CONSERVATION 142 (2009) 761771
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journal homepage: www.elsevier.com/locate/biocon
significant commercial or industrial infrastructure; United
Nations Development Programme et al., 2000).
Whilst the world’s population is growing increasingly iso-
lated from biodiversity as a result of urbanisation, evidence
is rapidly accruing as to the advantages that people gain from
experiencing and interacting with nature (Katcher and Beck,
1987; Kaplan andKaplan, 1989; Irvine andWarber, 2002; Maller
et al., 2005). The personal and societal benefits to human
health and well-being are wide ranging, but include quicker
recovery rates from ill-health (Ulrich, 1984), self-reported gen-
eral health (Stilgoe, 2001; de Vries et al., 2003; Maas et al.,
2006), longevity (Takano et al., 2002), stress-relief ( Moore,
1981; Leather et al., 1998; Parsons et al., 1998; Stigsdotter
and Grahn, 2004), reduced mental fatigue (Hartig et al., 1991;
Kuo, 2001), opportunities for reflection (Herzog et al., 1997;
Fuller et al., 2007), degree of social interaction (Sullivan
et al., 2004) and reduced crime rates (Kuo and Sullivan,
2001). Similarly, lack of access to green space has been asso-
ciated with higher levels of depression and anxiety (Macintyre
et al., 2003).
Improving urban environments for biodiversity will not
only be beneficial to human individuals and communities
inhabiting those areas, but will also be advantageous for bio-
logical conservation. In developed regions where intensive
use of the wider landscape, particularly through agriculture,
has resulted in population declines of species, urban areas
are becoming increasingly important for sustaining regional
abundances. Indeed, substantial proportions of the popula-
tions of some previously widespread and common species
now occur in urban environments (e.g., Beebee, 1997; Gregory
and Baillie, 1998; Mason, 2000; Bland et al., 2004; Peach et al.,
2004).
A variety of options is available to increase the environ-
mental quality of urban areas and, thereby, the degree of
interaction between people and nature, including creating
green networks and corridors, developing urban forests,
improving the management of public parks, and encouraging
householders to participate in ‘wildlife gardening’ (e.g., Baker,
1997; Tyrva
¨inen, 1997; Good, 2000; Savard et al., 2000; Beebee,
2001; DEFRA, 2002). Wildlife gardening can be broadly defined
to encompass any actions conducted in private or domestic
gardens to increase their suitability for wildlife, and thus in-
cludes the provision of a diversity of resources (e.g., sub-
strates, food, breeding and overwintering sites). A
significant proportion of urbanised areas comprise domestic
gardens (Loram et al., 2007), so one of the attractions of such
an approach to improving urban environments is the poten-
tial for mass participation by householders. The multiple
ownership of the domestic garden resource should be viewed
as an opportunity to be exploited, rather than the complica-
tion that it commonly presents in the context of other land
uses (Lepczyk et al., 2004; Gaston et al., 2005a; Warren et al.,
2008).
This said, the extent to which wildlife gardening activi-
ties are undertaken, and hence the level of provision of
important resources to enhance biodiversity, remains poorly
documented (but see Cowie and Hinsley, 1988; Lepczyk
et al., 2004; Gaston et al., 2005b, 2007; Buczacki, 2007). In
the UK, an assortment of estimates has been published
for different regions, most frequently in the popular media,
but seldom with any indication of how they were origi-
nally derived (e.g., Baines, 1985; Moss and Cottridge, 1998;
Owen, 1991; Bevan, 2001; Packham, 2001; Ryrie, 2003; Burton,
2004; Glue, 2006). In this paper we seek to redress this
situation, generating estimates for a selection of key re-
sources provided within domestic gardens across the coun-
try. This is the first time that such a comprehensive dataset
has been assembled to address this issue at a national
scale.
2. Materials and methods
2.1. Urban and suburban household/garden surveys
Twelve datasets were used to generate estimates of the
domestic garden resource in the UK (Tabl e 1). Eleven of
these were collected as part of seven recent projects that
have been conducted within urban and suburban areas
throughout the country (Fig. 1). They are highly representa-
tive of the UK population as approximately 90% of people
live in towns or cities (ODPM, 2001), with over 40%
distributed in London and other major cities (DETR, 2000).
Some of the surveys were household focused, whereas
others were more specifically aimed at garden users
(Tab le 1; the survey methods for the unpublished data
can be found in Appendix A of the Supplementary
material).
2.2. Survey of English Housing
The remaining dataset used in the calculations of garden re-
sources across the country was the Survey of English
Housing (SEH). It is an annual survey of approximately
20,000 households, stratified across the counties of England.
The SEH covers all types of household, from those in rural
areas and small towns through to city centres, therefore
accounting for potential variation at regional scales. It is
conducted for the UK government’s Department for Com-
munities and Local Government (formally part of the
Department for Transport, Local Government and the Re-
gions) by the National Centre for Social Research. The pri-
mary purpose of the survey is to collate reliable
information on the main features of each household and
the opinion of the respondents in relation to their personal
housing circumstances. In its entirety, the survey consists of
approximately 800 questions, comprising a core of factual
questions that remain largely unchanged from year to year
(e.g., regarding factors such as tenure, housing costs, hous-
ing history), in addition to a set of questions on attitudes
and intentions that are revised annually (see http://
www.esds.ac.uk/ for details).
The 2001/2002 survey (National Centre for Social Research
and Department for Transport, Local Government and the Re-
gions, 2004) included a small set of questions investigating
the degree to which households participate in wildlife garden-
ing activities. Respondents were asked: (i) whether they had
access to a garden or patio area and, if so, (ii) whether they
provided food for birds, (iii) if they had a nest box and (iv)
whether the garden contained a pond.
762 BIOLOGICAL CONSERVATION 142 (2009) 761771
Table 1 – Characteristics of each household/domestic garden survey included in this study, and the relevant garden resource data extracted. Details of the survey
methodologies for unpublished data can be found in Appendix A of the Supplementary material.
Survey name Year(s) of
survey
Area surveyed Survey methods (variables) Survey strategy Type of households
surveyed
Number of households/
gardens surveyed
(response rate, if
applicable)
Resources recorded
(measurement)
Reference
BUGS 1 (a) 2002 Sheffield GIS analysis (garden areas) Random All residential
households
250 households Garden (presence/absence)
Garden area (m
2
)
Gaston et al. (2005b)
BUGS 1 (b) 2002 Sheffield Telephone questionnaire
(garden features)
Random All residential
households
250 households (85%) Garden (presence/absence)
Nest boxes (presence/
absence) Ponds (presence/
absence) Trees >3 m tall
(count)
Gaston et al. (2005b)
BUGS 1 Extension 2002 Sheffield Telephone questionnaire
(garden features)
Random All residential
households
500 households (83%) Garden (presence/absence)
Supplementary bird food
provision (yes/no) Nest boxes
(presence/absence) Ponds
(presence/absence) Trees
>3 m tall (count)
K.J. Gaston et al.
(unpublished data)
BUGS 2 (a) 2005 Belfast Cardiff
Edinburgh Leicester
Oxford
GIS analysis (garden areas) Random Detached, semi-
detached and terraced
households
3643 gardens Garden area (m
2
)Loram et al. (2007)
BUGS 2 (b) 2004–2006 Belfast Cardiff
Edinburgh Leicester
Oxford
Garden visits (garden
features)
Informally stratified
sample, representative
of the range of
households, from a pool
of volunteered gardens
Detached, semi-
detached and terraced
households with rear
gardens
267 gardens Rear garden area (m
2
)
Supplementary bird food
provision (yes/no) Bird
feeders (presence/absence)
Nest boxes (presence/
absence) Ponds (coverage m
2
)
Trees >3 m tall (count)
A. Loram et al.
(unpublished data)
CityForm Project (a) 2004 Edinburgh Glasgow
Leicester Oxford
Sheffield
GIS analysis (garden areas) Census All residential
households
84,136 households Garden area (m
2
) R.A. Fuller et al.
(unpublished data)
CityForm Project (b) 2004 Sheffield GIS analysis (tree coverage) Census of 149 km
2
area All residential
households
Not determined Tree coverage (m
2
) R.A. Fuller et al.
(unpublished data)
CityForm Project (c) 2005 Edinburgh Glasgow
Leicester Oxford
Sheffield
Postal questionnaire (garden
features)
Random, stratified by
city area (inner, middle
and outer)
All residential
households
4381 households (37%) Garden (presence/absence)
Supplementary bird food
provision (yes/no) Bird
feeders (presence/absence)
Nest boxes (presence/
absence) Ponds (presence/
absence)
Gaston et al. (2007)
British Urban Domestic Cat
Survey
2004–2005 Twenty urban areas
across England and
Wales (Fig. 1)
Telephone questionnaire or
household visits (garden
features)
Random census of
twenty 1 km
2
squares
All residential
households
1000 households (33–
71%)
Garden (presence/absence)
Supplementary bird food
provision (yes/no) Nest boxes
(presence/absence)
Sims et al. (2008)
Sheffield Urban Domestic
Cat Project
2003–2005 Sheffield Telephone questionnaire or
household visits (garden
features)
Census of two 1 km
2
squares (one middle
and one outer city area)
Detached, semi-
detached and terraced
households
2782 households (61%) Garden (presence/absence)
Supplementary bird food
provision (yes/no) Bird
feeders (presence/absence)
V. Sims et al.
(unpublished data)
Valuing Open Space
Questionnaire
2006 Sheffield Postal questionnaire (garden
features)
Random, stratified by
socioeconomic
grouping
All residential
households (those
without access to a
garden were excluded)
2016 gardens (33%) Bird feeders (presence/
absence) Nest boxes
(presence/absence) Ponds
(presence/absence)
K.N. Irvine et al.
(unpublished data)
Survey of English Housing
(SEH)
2001–2002 England Household visits (garden
features)
Random, stratified by
Government Office
Region and
socioeconomic
grouping
All residential
households
19,913 households (67%) Garden (presence/absence)
Supplementary bird food
provision (yes/no) Nest boxes
(presence/absence) Ponds
(presence/absence)
NCSR and DETR (2004)
BIOLOGICAL CONSERVATION 142 (2009) 761771 763
Fig. 1 – The location of the urban and suburban areas sampled in seven of the household/domestic garden projects (Table 1),
the relevant survey data from which were collated for this study: (a) the UK cities targeted in six of the projects: B, Belfast; C,
Cardiff; E, Edinburgh; G, Glasgow; L, Leicester; O, Oxford; S, Sheffield; (b) the 20 1 km ·1 km areas sampled, in England and
Wales, for the British Urban Domestic Cat Survey: Bas, Basingstoke; Bd, Bridgend; Bs, Bristol; Bt, Bath; Ca, Cardiff; Ch, Chester;
Con, Conisbrough; Cov, Coventry; Cr, Croydon; Ep, Epsom; Gr, Greenwich; Ol, Oldham; Pl, Plymouth; Po, Pontypool; Pr, Preston;
Re, Reigate; Ru, Ruislip; Ur, Urmston; Wo, Woking; Wt, Walton-on-Thames.
764 BIOLOGICAL CONSERVATION 142 (2009) 761771
2.3. Estimating the extent of the garden resource
All surveys were weighted equally, although we acknowledge
that each individual survey will potentially have associated
biases. However, a broad range of research questions moti-
vated the different studies and a variety of methodological
techniques were used to collect the datasets. As such, there
is no reason to suspect that the garden resource estimates de-
rived from the surveys will be systematically biased. In
addition, the purpose of this paper is not to produce a highly
accurate figure for each resource, but to provide approximate,
robust and transparent estimates that can be used to
assess the value of domestic gardens to biodiversity
conservation.
Fig. 1 (continued)
BIOLOGICAL CONSERVATION 142 (2009) 761771 765
The garden resources examined were supplementary bird
feeding, provision of nest boxes, and the occurrence of ponds
and of trees taller than 3 m. For each dataset, the proportion
of households and/or gardens in the survey providing each re-
source was calculated, in addition to the average of any re-
corded quantitative measure (e.g., garden area, number of
trees). Data were then averaged across all studies to generate
a mean proportion and confidence interval for each resource
type (see Appendices B–F).
The number of households in the UK with access to a gar-
den was calculated by multiplying the mean proportion (gen-
erated using all surveys with relevant data) of households
with a garden by the number of households recorded in the
most recent UK census conducted in 2001 (Table 2 ). Subse-
quently, the area of all gardens across the country was extrap-
olated using the average garden size, which was recorded in
some of the surveys, and the previously estimated number
of gardens across the country. The number of households/gar-
dens in the UK providing each resource (e.g., supplementary
food for birds, a pond) was calculated using the same simple
assumptions; all household-based estimates were scaled up
using the 2001 census data, and all estimates of resources
specifically within gardens were extrapolated using the num-
ber of UK gardens derived above. The garden resource esti-
mates are hereafter presented as whole numbers, but were
calculated using exact figures.
3. Results
3.1. Garden sizes and total garden area
On average, 87% of households had a garden area associated
with the dwelling (Appendix B). Mean garden size, excluding
zero values within each survey, was 190 m
2
(95% CI = 173.0–
207.8). Extrapolating to the 26,159,440 households in the UK,
this equates to 22,738,563 (95% CI = 21,768,735–23,708,391)
domestic gardens with a total area of 432,964 ha (95%
CI = 393,391–472,537).
3.2. Supplementary food provision for birds
The average proportion of households and, more specifically,
households with a garden providing supplementary food for
birds were 48% and 51% respectively (Appendix C). Scaling
up, using the known number of households in the UK, this
gives an estimate of 12,581,718 (95% CI = 10,469,000–
14,694,435) homes across the country participating in bird
feeding activities. Similarly, using the proportion of house-
holds with a garden providing food for birds and the esti-
mated number of gardens in the UK, the extrapolated
number of gardens containing supplementary bird food is
11,640,921 (95% CI = 9,907,575–13,374,266).
The discrepancy between these two values is likely to be
due to the approximate nature of the calculations. However,
it is also possible that it reflects the provision of bird food
by householders living in flats, who may have access to an
outside space (e.g., a balcony or roof terrace) or a bird feeder
attached to a window in order to attract avian visitors, but
were excluded from the garden surveys.
From the surveys, a mean of 28% of households and 23% of
households with gardens specifically used bird feeders for
supplementary food provision. Assuming that each house-
hold/garden only has one bird feeder, which is likely to be a
conservative assumption, it is estimated that there are
7,376,105 (95% CI = 5,240,886–9,511,324) bird feeders associ-
ated with households at a national level and 5,299,590 (95%
CI = 3,132,608–7,475,571) bird feeders within gardens across
the UK.
3.3. Nest boxes
On average, 16% of households had at least one nest box
(Appendix D). Extrapolating this to the number of households
in the UK gives a minimum estimate of 4,305,621 (95%
CI = 2,658,848–5,952,394) nest boxes across the country. This
figure is consistent with the 4,710,632 (95% CI = 3,869,926–
5,551,337) nest boxes derived from a mean proportion of
21% of gardens containing a nest box.
3.4. Ponds
The mean proportion of households with a pond was 10%,
equating to 2,543,201 (95% CI = 1,487,803–3,598,599) ponds in
the country (Appendix E). The garden surveys, on average, re-
corded 16% of gardens containing a pond, giving a total of
3,531,118 (95% CI = 2,496,205–4,566,031) ponds in UK gardens.
The mean size of a garden pond was 1 m
2
(95% CI = 0.5–1.5).
Scaling up to the 3,531,118 gardens in the UK with a pond, this
corresponds to a total area of standing water of 349 ha (95%
CI = 158.5–540.3).
3.5. Trees
On average, 54% of gardens contained one or more trees taller
than 3 m, equating to 12,200,863 (95% CI = 9,846,431–
14,555,296) gardens across the UK (Appendix F). The mean
number of trees within a garden was 2.4 (95% CI = 1.8–2.9),
generating a national estimate of 28,730,986 trees within
domestic gardens (95% CI = 22,196,978–35,264,995). One study
examined the extent of tree cover in gardens, reporting that
11% of garden area was tree-covered; this figure translates
to a national tree coverage of 47,402 ha.
4. Discussion
4.1. Gardens
In the UK, we estimate that 87% of households, or 22.7 million
homes, have access to a domestic garden. These figures are
Table 2 – Number of households across the UK according
to the most recent census conducted in 2001.
Country Number of households
England 21,262,825
Northern Ireland 1,311,860
Scotland 2,308,939
Wales 1,275,816
UK 26,159,440
766 BIOLOGICAL CONSERVATION 142 (2009) 761771
comparable to the 85% of households in the UK that have a
garden according to English Nature (2004), but is somewhat
higher than the outdated estimate of 80% of households in
Britain quoted by Hessayon and Hessayon (1973) and subse-
quently cited in other ecological publications (e.g., Owen,
1991; Buczacki, 2007).
The average size of a garden in the surveys was 190 m
2
,
equating to an area of 432,964 ha across the country. Hessa-
yon and Hessayon (1973) give a mean area of 186 m
2
for gar-
dens which is highly consistent with our calculation, as is
the frequently quoted figure of over 400,000 ha of gardens in
Britain (e.g., Baines, 1985; Ryrie, 2003; Moss and Cottridge,
1998). To illustrate the extent of this area, it is equivalent to
the US state of Rhode Island and is larger than the English
county of Suffolk. To a householder, the area of their individ-
ual domestic garden may seem limited, particularly for those
living in terraced accommodation in urban centres, but the
sum of all these gardens contributes substantially to the over-
all amount of green space in urban areas across the country.
For example, Loram et al. (2007) found that domestic gardens
accounted for approximately one quarter of urban land cover
within five UK cities. Moreover, the total contiguous area, and
heterogeneous nature, of all the gardens in a residential street
or neighbourhood is of considerably more relevance to spe-
cies requiring large areas over which to fulfil their niche
requirements, than any one individual plot (e.g., Cannon
et al., 2005; Knight et al., 2005). As well as providing habitat
in their own right, domestic gardens may facilitate species
moving between areas of public green space (e.g., parks)
and/or the wider countryside, therefore increasing habitat
connectivity at a landscape-scale (Ferna
´ndez-Juricic, 2000;
Ferna
´ndez-Juricic and Jokima
¨ki, 2001; Rudd et al., 2002).
Nonetheless, the national coverage of domestic gardens is
still an order of magnitude less than the 4.7 million hectares
of statutory protected areas throughout the UK (S.F. Jackson
and R.A. Fuller, unpublished analyses). In addition, these esti-
mates of garden coverage may include large areas covered by
temporary structures, such as garden sheds or greenhouses,
or areas that have been converted to hard standing (e.g., con-
creted, paved, decked). Indeed, this is a growing phenomenon
(Goode, 2006), and a recent report has suggested that nearly
half of all households in North East England have paved over
the majority of their front gardens to create off-road parking
(RHS, 2007). Furthermore, the area of domestic gardens
throughout the UK is likely to decrease as a result of increas-
ing urbanisation. For example, the human population in Eng-
land alone is projected to grow by a further 7%, from
49 million individuals in 1998, to 52.4 million by 2021 (DETR,
2000). In response, new houses are being built at an increased
density of 40 dwellings per hectare, up from 25 dwellings per
hectare before 2002 (ODPM, 2006). Meanwhile, existing gar-
dens are frequently being built upon (commonly referred to
as backland development or ‘garden grabbing’) and thus pro-
portional coverage of green space within residential areas
seems likely to decline in the coming years (Goode, 2006).
4.2. Supplementary food provision for birds
Approximately 12.6 million households, or 48% of homes
across the UK, were estimated to be participating in supple-
mentary food provision for birds. This compares well to a poll
conducted in 2003 on behalf of the Royal Horticultural Society
that showed that half of all households with a garden provide
food for avian visitors (Moss, 2000).
Of the 12.6 million households supplying supplementary
food for birds, 7.4 million specifically use bird feeders. The
sheer scale of this resource estimate can best be illustrated
by an undoubtedly simplistic calculation. There are
134,602,702 (SE = 3,751,514) breeding birds in the UK and
67,734,400 (SE = 2,165,000) of these belong to species that
commonly use bird feeders (R.A Fuller, unpublished analyses
using national population estimates compiled by Baker et al.,
2006). Therefore, across the country, there is approximately
one bird feeder for every nine potentially feeder-using birds.
In recent years, bird feeding has developed from just
throwing food scraps out of the back door in winter to becom-
ing a multi-million pound industry (Moss and Cottridge, 1998;
Moss, 2000). Indeed, the British Trust for Ornithology (2006)
estimates that the total annual expenditure on outdoor bird
feeding in the UK is £200 million. The quantity of food held
by specially designed bird feeders across the country can be
roughly calculated as a typical small bird feeder contains
approximately 350 g of bird seed (R.A. Fuller, unpublished
data). Conservatively assuming that each household recorded
as using bird feeders only has the one, there is a standing crop
of 2580 tonnes of bird food. However, although this illustrates
the extent of the potential resource, up to 80% of feeders are
believed to be empty at any one time (Toms, 2003) and Gaston
et al. (2007) found that 36% of bird feeding activity was carried
out less frequently than once a month.
Moreover, supplementary feeding may not be universally
beneficial to all avian populations. Despite some evidence
that birds do not become dependent on food resources pro-
vided by householders (Brittingham and Temple, 1992), and
that levels of bird feeding are positively correlated with the
abundance of urban birds (Fuller et al., 2008), the possible
negative consequences still remain to be fully investigated
(Jones and Reynolds, 2008). These may include reliance on
an unpredictable resource, a reduction in diet quality, in-
creased predation pressure, loss of natural foraging behav-
iours (Brittingham and Temple, 1992; Robb et al., 2008) and
an increase in the number and abundance of exotic species
(Daniels and Kirkpatrick, 2006).
4.3. Nest boxes
At a national level, we estimated that there is a minimum of
4.7 million nest boxes within domestic gardens. This figure is
likely to be an underestimate as it assumes that each house-
hold only has one nest box, as none of the surveys collated
data on the number of nest boxes per household.
A review of 46 studies by Newton (1998) determined that
the availability of nesting sites can limit breeding bird densi-
ties for hole-nesting species. This can be a particular problem
in urban areas, where public land managers remove dead and
decaying trees and, along with them, the potential opportuni-
ties for nesting (Moss, 2000). As a result, it has been recom-
mended that nest boxes should be provided in urban parks
in order to increase the colonization by a greater variety of
cavity-nesting birds (Jokima
¨ki, 1999). Of the 134,602,702
BIOLOGICAL CONSERVATION 142 (2009) 761771 767
(SE = 3,751,514) breeding birds in the UK, 53,098,498
(SE = 1,929,443) belong to species that may commonly use gar-
den nest boxes as breeding sites (R.A. Fuller, unpublished
analyses using national population estimates compiled by
Baker et al., 2006). Using our conservative estimate of the
number of nest boxes in UK gardens, this approximates to
one nest box for every six breeding pairs of cavity-nesting
birds in the country. Even accounting for the fact that some
nest boxes will be structurally unsuitable, have been placed
in inappropriate locations, or not be in a serviceable state of
repair, this is still an impressive resource.
4.4. Ponds
Across the UK, we estimate that there are between 2.5 and
3.5 million ponds in domestic gardens, equating to 349 ha
of standing water. This corresponds to the over 2 million ci-
ted by Bevan (2001). To put these figures in context, the 1996
Lowland Pond Survey estimated that there were only 228,900
lowland ponds within the wider countryside of Great Britain
(Williams et al., 1998). Such ponds are defined as a small
water body between 1 m
2
and 2 ha, which holds water for
all or part of the year, and collectively includes pools, marl
and brick pits, bog pools, kettle holes and lagoons (Rouen,
2001). Following this definition, and excluding those within
gardens, they comprise 97% of the standing waters in the
country, but only 14% of the total surface area (Bailey-Watts
et al., 2000). Nonetheless, meaningful comparisons between
the numbers of ponds in gardens and those in the wider
countryside are difficult because most garden ponds are
generally much smaller (with a mean surface area of only
1m
2
).
In the wider countryside, many ponds are threatened by
natural succession, land drainage and development (Boothby
and Hull, 1997). Despite the total surface area of garden ponds
being so small, the resource is fragmented over a wide distri-
bution and provides a haven for many amphibians, inverte-
brates and plants in residential areas, including some of
specific conservation interest (e.g., the common frog Rana
temporaria and common toad Bufo bufo;Beebee, 1997; Williams
et al., 2000). Indeed, almost all ponds are used by aquatic
organisms, irrespective of age or structure, as long as the
water quality is maintained (Pond Action, 1994; Linton and
Goulder, 2000; Wood et al., 2003), and they do not have to be
large to be of high conservation value (Oertli et al., 2002). Gar-
den ponds also provide birds with drinking water and a place
to bathe, in addition to supporting a variety of invertebrates
which are a possible food resource (Moss, 2000; Burton,
2004). The important habitat heterogeneity associated with
domestic garden ponds is often lost due to the removal of veg-
etation and silt (Biggs et al., 1994). A balance therefore needs
to be found between maintaining the pond and preventing
succession without over managing the resource (Linton and
Goulder, 2000).
4.5. Trees
Over 12 million gardens across the country are estimated to
contain at least one tree. Of these gardens, the average num-
ber of trees in each was approaching 2.4, giving a total esti-
mate of 28.7 million trees. According to the Forestry
Commission (2003), there are just over 123 million live trees
occurring outside woodland in Great Britain (England,
89,217,000; Scotland, 18,576,900; Wales, 15,334,000) and a fur-
ther 2 million dead trees. Domestic gardens therefore contrib-
ute just under a quarter of this total.
Trees in residential areas can play a number of important
roles. First, they contribute to ecosystem services such as
microclimate regulation and air filtration (Bolund and Hun-
hammar, 1999). Second, garden trees may include rare species
that have either disappeared, or been severely depleted, in the
wider countryside, often as a result of changing land use (e.g.,
old varieties of fruit trees). Finally, they may provide impor-
tant habitats for wildlife. For instance, the species richness
of some taxonomic groups increases in urban areas in rela-
tion to the volume of available vegetation (Dickman, 1987;
Jokima
¨ki and Suhonen, 1993; Savard et al., 2000) and trees
provide nesting sites, food and refuge from predators for
many species (Ferna
´ndez-Juricic and Jokima
¨ki, 2001).
Although the utility of trees within domestic gardens as hab-
itats, particularly in urban centres, will frequently be limited
by an array of factors such as human disturbance, stress as a
result of pollution or heat, and whether they are exotic or na-
tive species, this is still a potentially substantial resource for
biodiversity that has, so far, largely been overlooked in the
conservation literature.
5. Conclusions
The potential importance of domestic gardens to biodiversity
has been acknowledged in the popular media for many years
(e.g., Hammond, 1974; Baines, 1985; Good, 2000; Packham,
2001; Ryrie, 2003; Buczacki, 2007). This assertion is supported
by a small number of studies that have demonstrated that
gardens play a substantial role in maintaining, and enhanc-
ing, biodiversity. They have included intensive investigations
of the biodiversity of individual gardens (e.g., Owen, 1991;
Miotk, 1996), the presence and abundance of particular tax-
onomic groups in one or more gardens (e.g., Morley, 1944;
Barnes, 1949; Davis, 1978; Dickman, 1987; Rapoport, 1993;
Vickery, 1995; Cannon et al., 2005; Daniels and Kirkpatrick,
2006; Smith et al., 2005a–c; Osborne et al., 2008), and the
occurrence of multiple taxonomic groups across many gar-
dens (e.g., Saville, 1997; Thompson et al., 2003, 2004; Gaston
et al., 2005a). However, further research is required to better
understand the complex interactions between wildlife, both
native and exotic, and the habitat features provided within
gardens. Knowing how best to manage these resources must
be a priority if we are to maximise the retention of biodiver-
sity within domestic gardens in the future. To date, informa-
tion on the magnitude of the resource provision has also
been lacking (Gaston et al., 2005b; Loram et al., 2007; Buc-
zacki, 2007). This paper is the first to illustrate the sheer
scale of the contribution that gardens make to possible hab-
itat provision in a national context. Planning strategies
which neglect the role of gardens within estimates of green
space, particularly those in urban areas, undervalue the ex-
tent of the resource. This is particularly pertinent as further
development and urbanisation throughout the world is likely
to continue unabated.
768 BIOLOGICAL CONSERVATION 142 (2009) 761771
Acknowledgements
This work was funded by the Engineering and Physical Sci-
ences Research Council (through the CityForm research con-
sortium) and the Countryside Council for Wales, Department
for Environment, Food and Rural Affairs, Environment and
Heritage Service, English Nature and Scotland and Northern
Ireland Forum for Environmental Research (through the BUGS
II project). K.J. Gaston holds a Royal Society Wolfson Research
Merit Award. We also wish to acknowledge the National Cen-
tre for Social Research (data collectors), Department for Trans-
port, Local Government and the Regions (sponsor) and the UK
Data Archive (data distributor) for providing the Survey of Eng-
lish Housing (SEH) 2001/2002 dataset. Crown copyright mate-
rial is reproduced with the permission of the Controller of
HMSO and the Queen’s printer for Scotland. These organisa-
tions bear no responsibility for the data analysis or interpreta-
tion of findings stated within this publication. MasterMap data
were kindly supplied by Ordnance Survey, by license through
the CityForm Consortium. We are grateful to members of the
CityForm Consortium, S. Berry (Natural England), N. Burke
and D. Lewis (Sheffield City Council), R. Davies, I. Fishburn,
C. Gascoigne, A. Holt, S. Jackson, M. McKenna (Environment
and Heritage Service), J. Tratalos, R. Schaible (Department of
Agriculture and Rural Development) and K. Watts (Forest Re-
search) for collecting and/or supplying data. We also extend
our thanks to M. Dallimer and S. Davies for suggestions and
constructive discussion in relation to the manuscript, and to
four anonymous reviewers for their comments.
Appendix A. Supplementary material
Supplementary data associated with this article can be found,
in the online version, at doi:10.1016/j.biocon.2008.12.016.
REFERENCES
Bailey-Watts, T., Lyle, A., Battarbee, R., Harriman, R., Biggs, J., 2000.
Lakes and ponds. In: Acreman, M. (Ed.), The Hydrology of the
UK: A Study of Change. Routledge, London, pp. 180–203.
Baines, C., 1985. How to Make a Wildlife Garden. Elm Tree Books,
London.
Baker, G., 1997. A Framework for the Future: Green Networks with
Multiple Uses In and Around Towns and Cities. English Nature
Report 256. English Nature, Peterborough.
Baker, H., Stroud, D.A., Aebischer, N.J., Cranswick, P.A., Gregory,
R.D., McSorley, C.A., Noble, D.G., Rehfisch, M.M., 2006.
Population estimates of birds in Great Britain and the United
Kingdom. British Birds 99, 25–44.
Barnes, H.F., 1949. The slugs in our gardens. New Biologist 6, 29–
49.
Beebee, T.J.C., 1997. Changes in dewpond numbers and
amphibian diversity over 20 years on chalk downland in
Sussex, England. Biological Conservation 81, 215–219.
Beebee, T.J.C., 2001. British wildlife and human numbers: the
ultimate conservation issue? British Wildlife 13, 1–8.
Bevan, D., 2001. Creating a Garden Wildlife Pond. Ringpress Books,
Lydney, Gloucestershire.
Biggs, J., Corfield, A., Walker, D., Whitfield, M., Williams, P., 1994.
New approaches to the management of ponds. British Wildlife
5, 273–287.
Bland, R.L., Tully, J., Greenwood, J.J.D., 2004. Birds breeding in
British gardens: an underestimated population? Bird Study 51,
96–106.
Bolund, P., Hunhammar, S., 1999. Ecosystem services in urban
areas. Ecological Economics 29, 293–301.
Boothby, J., Hull, A.P., 1997. A census of ponds in Cheshire, North
West England. Aquatic Conservation: Marine and Freshwater
Ecosystems 7, 75–79.
British Trust for Ornithology, 2006. We Spend £200 Million a Year
on Wild Bird Food, British Trust for Ornithology Press Release
No. 2006/12/76. British Trust for Ornithology Press, Thetford.
Brittingham, M.C., Temple, S.A., 1992. Does winter bird feeding
promote dependency? Journal of Field Ornithology 63, 190–
194.
Buczacki, S., 2007. Garden Natural History. Harper Collins
Publishers, London.
Burton, R., 2004. RSPB Pocket Birdfeeder Guide. Dorling
Kindersley, London.
Cannon, A.R., Chamberlain, D.E., Toms, M.P., Hatchwell, B.J.,
Gaston, K.J., 2005. Trends in the use of private gardens by wild
birds in Great Britain 1995–2002. Journal of Applied Ecology 42,
659–671.
Cowie, R.J., Hinsley, S.A., 1988. The provision of food and the use
of bird feeders in suburban gardens. Bird Study 35, 163–168.
Daniels, G.D., Kirkpatrick, J.B., 2006. Does variation in garden
characteristics influence the conservation of birds in
suburbia? Biological Conservation 133, 326–335.
Davis, B.N.K., 1978. Urbanisation and the diversity of insects. In:
Mound, L.A., Waloff, N. (Eds.), Diversity of Insect Faunas.
Blackwell Scientific, Oxford, pp. 126–138.
DEFRA, 2002. Working With the Grain of Nature. DEFRA
Publications, London.
DETR, 2000. Our Towns and Cities: The Future – Full Report.
Department of Transport and the Regions, London.
de Vries, S., Verheij, R.A., Groenewegen, P.P., Spreeuwenberg, P.,
2003. Natural environments – healthy environments? An
exploratory analysis of the relationship between green space
and health. Environment and Planning A 35, 1717–1731.
Dickman, C.R., 1987. Habitat fragmentation and vertebrate
species richness in an urban environment. Journal of Applied
Ecology 24, 337–351.
English Nature, 2004. Get Green Fingers Online with a Virtual
Garden Tour. <www.english-nature.org.uk/nature_in_the_
garden/fun.asp> (accessed 15.08.08).
Ferna
´ndez-Juricic, E., 2000. Avifaunal use of wooded streets in an
urban landscape. Conservation Biology 14, 513–531.
Ferna
´ndez-Juricic, E., Jokima
¨ki, J., 2001. A habitat island approach
to conserving birds in urban landscapes: case studies from
southern and northern Europe. Biodiversity and Conservation
10, 2023–2043.
Forestry Commission, 2003. National Inventory of Woodland and
Trees – Great Britain. Forestry Commission, Edinburgh.
Fuller, R.A., Irvine, K.N., Devine-Wright, P., Warren, P.H., Gaston,
K.J., 2007. Psychological benefits of green space increase with
biodiversity. Biology Letters 3, 390–394.
Fuller, R.A., Warren, P.H., Armsworth, P.R., Barbosa, O., Gaston,
K.J., 2008. Garden bird feeding predicts the structure of urban
avian assemblages. Diversity and Distributions 14, 131–137.
Gaston, K.J., Smith, R.M., Thompson, K., Warren, P.H., 2005a.
Urban domestic gardens (II): experimental tests of methods
for increasing biodiversity. Biodiversity and Conservation 14,
395–413.
Gaston, K.J., Warren, P.H., Thompson, K., Smith, R.M., 2005b.
Urban domestic gardens (IV): the extent of the resource and its
associated features. Biodiversity and Conservation 14, 2249–
3327.
Gaston, K.J., Fuller, R.A., Loram, A., MacDonald, C., Power, S.,
Dempsey, N., 2007. Urban domestic gardens (XI): variation in
BIOLOGICAL CONSERVATION 142 (2009) 761771 769
urban wildlife gardening in the UK. Biodiversity and
Conservation 16, 3227–3238.
Glue, D., 2006. Variety at winter bird tables. Bird Populations 7,
212–215.
Good, R., 2000. The value of gardening for wildlife. What
contribution does it make to conservation? British Wildlife 12,
77–84.
Goode, D., 2006. Green Infrastructure. Report to the Royal
Commission on Environmental Pollution, London.
Gregory, R.D., Baillie, S.R., 1998. Large-scale habitat use of some
declining British birds. Journal of Applied Ecology 35, 785–799.
Hammond, P.M., 1974. Changes in the British Coleopterous fauna.
In: Hawksworth, D.L. (Ed.), The Changing Flora and Fauna of
Britain. Academic Press, London, pp. 323–369.
Hartig, T., Mang, M., Evans, G.W., 1991. Restorative effects of
natural environment experiences. Environment and
Behaviour 23, 3–26.
Herzog, T.R., Black, A.M., Fountaine, K.A., Knotts, D.J., 1997.
Reflection and attentional recovery as distinctive benefits of
restorative environments. Journal of Environmental
Psychology 17, 165–170.
Hessayon, D.G., Hessayon, J.P., 1973. The Garden Books of Europe.
Elm Tree Books, London.
Irvine, K.N., Warber, S.L., 2002. Greening healthcare: practicing as
if the natural environment really mattered. Alternative
Therapies in Health and Medicine 8, 76–83.
Jokima
¨ki, J., 1999. Occurrence of breeding bird species in urban
parks: effects of park structure and broad scale variables.
Urban Ecosystems 3, 21–34.
Jokima
¨ki, J., Suhonen, J., 1993. Effects of urbanization on the
breeding bird species richness in Finland: a biogeographical
comparison. Ornis Fennica 70, 71–77.
Jones, D.N., Reynolds, S.J., 2008. Feeding birds in our towns and
cities: a global research opportunity. Journal of Avian Biology
39, 265–271.
Kaplan, R., Kaplan, S., 1989. The Experience of Nature: A
Psychological Perspective. Cambridge University Press,
Cambridge.
Katcher, A., Beck, A., 1987. Health and caring for living things.
Anthrozoos 1, 175–183.
Knight, M.E., Martin, A.P., Bishop, S., Osborne, J.L., Hale, R.J.,
Sanderson, R.A., Goulson, D., 2005. An interspecific
comparison of foraging range and nest density of four
bumblebee (Bombus) species. Molecular Ecology 14, 1811–1820.
Kuo, F.E., 2001. Coping with poverty: impacts of environment and
attention in the inner city. Environment and Behaviour 33, 5–
34.
Kuo, F.E., Sullivan, W.C., 2001. Environment and crime in the inner
city. Does vegetation reduce crime? Environment and
Behaviour 33, 343–367.
Leather, P., Pyrgas, M., Beale, D., Lawrence, C., 1998. Windows in
the workplace. Environment and Behaviour 30, 739–763.
Lepczyk, C.A., Mertug, A.G., Liu, J., 2004. Assessing landowner
activities related to birds across rural-to-urban landscapes.
Environmental Management 33, 110–125.
Linton, S., Goulder, R., 2000. Botanical conservation value related
to origin and management of ponds. Aquatic Conservation:
Marine and Freshwater Ecosystems 10, 77–91.
Loram, A., Tratalos, J., Warren, P.H., Gaston, K.J., 2007. Urban
domestic gardens (X): the extent and structure of the resource
in five major cities. Landscape Ecology 22, 601–615.
Maas, J., Verheij, R.A., Groenewegen, P.P., de Vries, S.,
Spreeuwenberg, P., 2006. Green space, urbanity, and health:
how strong is the relation? Journal of Epidemiology and
Community Health 60, 587–592.
Macintyre, S., Ellaway, A., Hiscock, R., Kearns, A., Der, G., McKay,
L., 2003. What features of the home and the area might help to
explain observed relationships between housing tenure and
health: evidence from the west of Scotland. Health and Place
9, 207–218.
Maller, C., Townsend, M., Pryor, A., Brown, P., St. Leger, L., 2005.
Healthy nature healthy people: ‘contact with nature’ as an
upstream health promotion intervention for populations.
Health Promotion International 21, 45–54.
Mason, C.F., 2000. Thrushes now largely restricted to the built
environment in eastern England. Diversity and Distributions 6,
189–194.
McKinney, M.L., 2002. Urbanization, biodiversity, and
conservation. Bioscience 52, 883–890.
Meyer, W.B., Turner, B.L., 1992. Human population growth and
global land-use cover change. Annual Review of Ecology and
Systematics 23, 6–39.
Miller, J.R., 2005. Biodiversity conservation and the extinction of
experience. Trends in Ecology and Evolution 20, 430–434.
Miotk, P., 1996. The naturalized garden – a refuge for animals? –
first results. Zoologischer Anzeiger 235, 101–116.
Moore, E.O., 1981. A prison environment’s effect on health care
service demands. Journal of Environmental Systems 11, 17–
34.
Morley, B.D.W., 1944. A study of the ant fauna of a garden, 1934–
42. Journal of Animal Ecology 13, 123–127.
Moss, S., 2000. Bird-Friendly Garden: A Practical Month-by-Month
Guide to Attracting Birds to Your Garden. Harper Collins
Publishers, London.
Moss, S., Cottridge, D., 1998. Attracting Birds to Your Garden. New
Holland Publishers, London.
National Centre for Social Research and Department for
Transport, Local Government and the Regions, 2004. Survey of
English Housing, 2001–2002. SN: 5021. UK Data Archive,
Colchester, Essex.
Newton, I., 1998. Population Limitation in Birds. Academic Press,
London.
ODPM, 2001. Habitat UK National Report. Office of the Deputy
Prime Minister, London.
ODPM, 2006. Land Use Change in England: Residential
Development to 2004 – January update. Office of the Deputy
Prime Minister, London.
Oertli, B., Joye, D.A., Castella, E., Juge, R., Cambin, D., Lachavanne,
J.-B., 2002. Does size matter? The relationship between pond
area and biodiversity. Biological Conservation 104, 59–70.
Osborne, J.L., Martin, A.P., Shortall, C.R., Todd, A.D., Goulson, D.,
Knight, M.E., Hale, R.J., Sanderson, R.A., 2008. Quantifying and
comparing bumblebee nest densities in gardens and
countryside habitats. Journal of Applied Ecology 45, 784–792.
Owen, J., 1991. The Ecology of a Garden: The First Fifteen Years.
Cambridge University Press, Cambridge.
Packham, C., 2001. Back Garden Nature Reserve. New Holland
Publishers, London.
Parsons, R., Tassinary, L.G., Ulrich, R.S., Hebl, M.R., Grossman-
Alexander, M., 1998. The view from the road: implications for
stress recovery and immunisation. Journal of Environmental
Psychology 18, 113–140.
Peach, W.J., Denny, M., Cotton, P.A., Hill, I.F., Gruar, D., Barritt, D.,
Impet, A., Mallord, J., 2004. Habitat selection by song thrushes
in stable and declining farmland populations. Journal of
Applied Ecology 41, 275–293.
Pond Action, 1994. The Oxfordshire Pond Survey: A Report to the
World Wide Fund for Nature UK. Oxford Brookes University,
Oxford.
Pyle, R.M., 2003. Nature matrix: reconnecting people and nature.
Oryx 37, 206–214.
Rapoport, E.H., 1993. The process of plant colonization in small
settlements and large cities. In: McDonnell, M.J., Pickett, S.T.A.
(Eds.), Humans as Components of Ecosystems: The Ecology of
Subtle Human Effects and Populated Areas. Springer-Verlag,
New York, pp. 190–207.
770 BIOLOGICAL CONSERVATION 142 (2009) 761771
RHS, 2007. Gardening Matters. Royal Horticultural Society,
London.
Robb, G.N., McDonald, R.A., Chamberlain, D.E., Bearhop, S., 2008.
Food for thought: supplementary feeding as a driver of
ecological change in avian populations. Frontiers in Ecology
and the Environment 6, 476–484.
Rouen, K., 2001. Use of the terms ‘ponds’ and ‘pools’. Freshwater
Forum 17, 4.
Rudd, H., Vala, J., Schaefer, V., 2002. Importance of backyard
habitat in a comprehensive biodiversity conservation strategy:
a connectivity analysis of urban green spaces. Restoration
Ecology 10, 368–375.
Ryrie, C., 2003. Wildlife Gardening. Cassell Illustrated, London.
Savard, J.-P.L., Clergeau, P., Mennechez, G., 2000. Biodiversity
concepts and urban ecosystems. Landscape and Urban
Planning 48, 131–142.
Saville, B., 1997. The Secret Garden: Report of the Lothian Secret
Garden Survey. Lothian Wildlife Information Centre,
Edinburgh.
Sims, V., Evans, K.L., Newson, S.E., Tratalos, J., Gaston, K.J., 2008.
Avian assemblage structure and domestic cat densities in
urban environments. Diversity and Distributions 14, 387–399.
Smith, R.M., Gaston, K.J., Warren, P.H., Thompson, K., 2005a.
Urban domestic gardens (VIII): environmental correlates of
invertebrate species abundance. Biodiversity and
Conservation 15, 2515–2545.
Smith, R.M., Thompson, K., Hodgson, J.G., Warren, P.H., Gaston,
K.J., 2005b. Urban domestic gardens (IX): composition and
richness of the vascular plant flora, and implications for
native biodiversity. Biological Conservation 129, 312–322.
Smith, R.M., Warren, P.H., Thompson, K., Gaston, K.J., 2005c.
Urban domestic gardens (VI): environmental correlates of
invertebrate species richness. Biodiversity and Conservation
15, 2415–2438.
Stilgoe, J.R., 2001. Gone barefoot lately? American Journal of
Preventative Medicine 20, 243–244.
Stigsdotter, U.A., Grahn, P., 2004. A garden at your workplace may
reduce stress, In: Dilani, A. (Ed.), Design and Health III – Health
Promotion through Environmental Design Research Centre for
Design and Health, Stockholm, pp. 147–157.
Sullivan, W.C., Kuo, F.E., DePooter, S.F., 2004. The fruit of urban
nature: vital neighbourhood spaces. Environment and
Behaviour 36, 678–700.
Takano, T., Nakamura, K., Watanabe, M., 2002. Urban residential
environments and senior citizens longevity in megacity areas:
the importance of walkable green spaces. Journal of
Epidemiology and Community Health 56, 913–918.
Thompson, K., Austin, K.C., Smith, R.H., Warren, P.H., Angold,
P.G., Gaston, K.J., 2003. Urban domestic gardens (I): putting
small-scale plant diversity in context. Journal of Vegetation
Science 14, 71–78.
Thompson, K., Hodgson, J.G., Smith, R.M., Warren, P.H., Gaston,
K.J., 2004. Urban domestic gardens (III): composition and
diversity of lawn floras. Journal of Vegetation Science 15, 371–
376.
Toms, M., 2003. The BTO/CJ Garden Birdwatch Book. British Trust
for Ornithology, Thetford.
Tyrva
¨inen, L., 1997. The amenity value of the urban forest: an
application of the hedonic pricing method. Landscape and
Urban Planning 37, 211–222.
Ulrich, R.S., 1984. View through a window may influence recovery
from surgery. Science 224, 420–421.
United Nations, 2007. World Population Prospects: The 2006
Revision. United Nations, New York.
United Nations Development Programme, United Nations
Environment Programme, World Bank, World Resources
Institute, 2000. World Resources 2000–2001: People and
Ecosystems – The Fraying Web of Life. Elsevier Science,
Amsterdam.
Vickery, M.L., 1995. Gardens: The neglected habitat. In: Ecology
and Conservation of Butterflies. Chapman and Hall, London,
pp. 123–134.
Warren, P.S., Lerman, S.B., Charney, N.D., 2008. Plants of a feather:
spatial autocorrelation of gardening practices in suburban
neighbourhoods. Biological Conservation 141, 3–4.
Williams, P., Biggs, J., Barr, C.J., Cummins, C.P., Gillespie, M.K.,
Rich, T.C.G., Baker, A., Baker, J., Beesley, J., Corfield, A., Dobson,
D., Culling, A.S., Fox, G., Howard, D.C., Luursema, K., Rich, M.,
Samson, D., Scott, W.A., White, R., Whitfield, M., 1998. Lowland
Pond Survey 1996. Department of Environment, Transport and
the Regions, London.
Williams, P., Biggs, J., Whitfield, M., Thorne, A., Bryant, S., Fox, G.,
Nicolet, P., 2000. The Pond Book: A Guide to the Management
and Creation of Ponds. The Pond Conservation Trust, Oxford.
Wilson, E.O., 1984. Biophilia. Harvard University Press,
Massachusetts.
Wood, P.J., Greenwood, M.T., Agnew, M.D., 2003. Pond biodiversity
and habitat loss in the UK. Area 35, 206–216.
BIOLOGICAL CONSERVATION 142 (2009) 761771 771
... For those species that can adapt to urban areas, a large amount of habitat is available because whilst individual parks and gardens may appear inconsequential, the total amount of green space and associated resources is considerable 17,18 . For example, it is estimated that in the United Kingdom alone, more than 12.6 million householders provide food for birds in their gardens 19 , whilst more than 4.7 million nest boxes are provided in gardens 19 . ...
... For those species that can adapt to urban areas, a large amount of habitat is available because whilst individual parks and gardens may appear inconsequential, the total amount of green space and associated resources is considerable 17,18 . For example, it is estimated that in the United Kingdom alone, more than 12.6 million householders provide food for birds in their gardens 19 , whilst more than 4.7 million nest boxes are provided in gardens 19 . ...
... To our knowledge, the smallest garden sizes in which insects were studied that focus on insect were in urban grasslands, using plots of flowering plants ranging from 1 to 100 m 2 and showing a positive correlation between area and insect flower-visitor diversity (Blaauw & Isaacs, 2014). Considering that a substantial amount of the UGS in cities are relatively small, they may contribute strongly to the urban biodiversity (Baker et al., 2018;Davies et al., 2009). With the increasingly limited space in the dense urban environment (Vergnes et al., 2014;Haaland and van Den Bosch, 2015), not large garden size, but rather the area of vegetation, and thus habitat, maybe a more mechanistic and manageable driver than garden size, but this has not been properly investigated. ...
... These studies suggest that certain design features of gardens attract and support biodiversity better than others. Therefore, it is urgent to understand what design features of urban gardens are favoured by insect communities in cities. Especially given that this information can be used by policymakers and citizens, as they seem willing to support wildlife, so that we can support insects from cities across the globe (Davies et al., 2009). ...
... Furthermore, environmental seasonality can also modify the conditions of urban green spaces in tropical areas and, consequently, affect their ability to support populations of different bird species (e.g., Schütz and Schulze 2018;Mac-Gregor-Fors et al. 2021). Urban green areas often include spaces for recreational human activities (e.g., yard games, exercise, picnics, festivals, etc.) that also provide water sources, food leftovers, and shelters to wild animal populations consistently throughout the year (Davies et al. 2009). To develop successful conservation strategies focused on urban green areas, we must understand how the characteristics of urban parks facilitate the presence of a relatively high number of species, as well as the particular season of the year when bird diversity is highest. ...
... Consistent with our hypothesis, species richness was higher in the dry season. Green areas in urban landscapes are frequented by different bird species because they offer shelter, food, and water, which are scarce resources in the surrounding forests during the dry season (Davies et al. 2009). A study across 18 urban parks in southern China found similar results, with higher richness and abundance of native birds estimated during the winter months (January to February) when resources are scarce as compared to the breeding season (July to August; Xie et al. 2022). ...
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Urban growth often leads to land-use changes that result in biodiversity loss and reduced human benefits. In urban zones, green areas facilitate physicochemical processes (such as carbon capture, reducing environmental temperature and noise pollution), offer multiple benefits to human beings (e.g., water filtration and purification), and support numerous vertebrate populations, including birds. In the tropics, the capacity of green spaces to maintain bird populations is regulated by characteristics of these areas (e.g., vegetation structure) and environmental seasonality. In order to generate ecological knowledge to help conserve bird diversity in large urban settlements, this study aimed to (1) identify the most influential variables on the distribution of bird species in green areas of a tropical megacity, and (2) assess how bird richness varies between the dry and rainy seasons. Across two dry and rainy seasons between 2021 and 2022, detection records of 108 bird species were obtained from 101 green areas. Air temperature and sampling time were the primary factors influencing bird detection. Bird occupancy and richness were higher in parks near other green areas in first dry and increased with tree richness during the rainy seasons. Floral abundance explained the occupancy and richness in the second dry season. In 2021, the highest richness was observed during the dry season, while in 2022, the highest richness was estimated during the rainy season. These findings highlight the importance of resource availability and spatial arrangement in urban green areas for bird diversity, offering insights for conservation and maintaining ecosystem benefits in urban environments.
... Most studies using bird guilds as models Marzluff, 2016) indicated generalist species of birds as better adapted to urban environments than bird specialists. The fact that avian food sources in urban habitats predominantly consist of seeds and other various plant material (Davies et al., 2009) may be a reason why insectivorous bird species appear to be scarce in urban areas then birds from other guilds (Kark et al., 2007;Máthé & Batáry, 2015). However, Evans et al. (2011), based on the measurement of bird species´ responses to urban development in Britain using a continuous quantitative index, revealed little evidence that urban development clearly selected against long-distance migrants, insectivores, and bird species limited by dispersal capacity. ...
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Environmental sustainability and resilience of cities is based on the biological diversity of green urban areas. Biodiversity of green infrastructure in dynamic urbanized environments is changing very fast. Understanding these ecological processes (and using them to environmental management of urban ecosystems) supports the application of birds as bioindicators. Although there is a consensus that long-term bird studies are extraordinarily valuable for better understanding of real temporal trends in avian urban diversity changes, these are still very rare. The main aim of this study is the assessment of long-term changes (during 30 years) in avian communities in historic manor parks in Central-European urbanized landscapes. Statistical testing of hypotheses as well as using calculation of faunistic indexes based on guild approach revealed high stability in bird diversity of large historic manor parks for a period 1994–2023. Results revealed the role of historic manor parks not only as historical sites but also as important urban biodiversity hotspots, which need specific management practice to maintain biodiversity in environmentally sustainable cities. Results also supported our better understanding of the joining of natural and historical heritage in cities worldwide in the frame of new scientific concept of Biocultural Diversity.
... Urban woodlands, for example, can maintain ecosystem functions similar to those of more natural communities, despite being highly modified (Roy et al. 1999;Croci et al. 2008). Domestic gardens comprise approximately 25% of urban landscapes in the UK and many other developed regions in the global north , and can provide valuable wildlife habitat (Davies et al. 2009), although there is much variation in how wildlife-friendly gardens are (Larson et al. 2022). ...
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Scavenging removes carrion or littered food waste from the environment, promoting nutrient cycling, and reducing waste management costs. These ecosystem services are important in urban environments, where high human population densities result in increased littered food waste. It is unclear how the magnitude of scavenging across urban-rural gradients is influenced by agent, land-cover type, and patch size. We investigated scavenging provision by vertebrates and invertebrates across a gradient of urbanisation, based on impervious surface cover, in woodlands and gardens in Liverpool, UK. The percentage dry weight loss of bait after 48 h, deployed within vertebrate exclusion cages or exposed to vertebrates and invertebrates, was used to quantify scavenging provision. General linear mixed effects models were used to assess the relative contributions of vertebrates and invertebrates across an urban-rural gradient, variation in scavenging between woodlands and gardens, and the effects of semi-natural vegetation cover on scavenging in gardens. We consider patch size as a preliminary assessment of how fragmentation influences scavenging. Vertebrates contributed substantially more to scavenging than invertebrates across the urbanisation gradient. Vertebrate scavenging was greater in woodlands than gardens, while invertebrate scavenging remained consistent. Scavenging increased with patch size in gardens, but not woodlands. Vertebrate scavenging increased with patch size and garden semi-natural vegetation cover. Urban woodlands and gardens make important contributions to scavenging-mediated ecosystem services. There is a need to increase the cover of semi-natural vegetation in gardens to increase their contributions, and protect and expand woodlands, especially in areas with a high demand for scavenging-mediated ecosystem services.
... Leaves are the major eco-physiological parts of a plant that interact with the atmosphere [16] and FG had a significant effect on the LAI of grain amaranth at Wudil 2022. The significant differences observed from the LAI due to the foliar application of FG tea fertilizer to the leaves were in agreement with the assertions of Davies [17] who stated that FG is a high-quality organic fertilizer that contains natural ingredients that can promote vigorous growth for outdoor vegetables, flowers, fruit, trees, ornamental plants, and indoor houseplants. The PAR and RWC were significantly affected by FG at BUK. Fish guano deposition and absorption by the leaves may have altered some cellular functions of the plant which causes the stomata to close, as in the water deficit case [18]. ...
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Field trials were conducted during the 2021 and 2022 at the Teaching and Research Farm of the Facultyof Agriculture Bayero University Kano (110 97′ 98.6′′N 80 42′03.7′′'E) and Research Farm of Aliko Dangote University of Science and Technology Wudil (11̊25′N 9̊E) to determine the impact of fish guano (FG) and abscisic acid (ABA) leaf area index (LAI), stomatal conductance(SC), photosynthetic active radiation (PAR) and relative water content (RWC) of grain amaranth under moisture stress conditions. Treatments consisted of moisture stress stages (vegetative, flowering and grain filling), FG (0, 0.1 and 0.2kg) and ABA concentrations (0, 20and 50 µmolL-1) and laid out in a split-plot design and replicated three times. Moisture stress was applied in the main plots, while FG and ABA treatments were applied in the subplots. Data was collected on LAI, SC, PAR and RWC and subjected to analysis of variance (ANOVA) using GENSTAT 17th edition software. Significant treatment means were separated using the Student Newman Keuls Test (SNK) at 5% probability level. In 2021 and 2022, the LAI and RWC of the plants at BUK and Wudil were significantly (p<0.001) boosted by the application of 0.2 kg FG levels and 50 µmolL-1 ABA. In the 2021 season, plants experiencing moisture stress during flowering exhibited significantly (p<0.05) higher RWC at BUK. Additionally, the application of 20 µmolL-1 ABA had a significant (p<0.05) effect on stomatal conductance at BUK and Wudil in both seasons. The results of this study suggested that FG and ABA could be useful strategies for improving the performance and resilience of grain amaranth crops in the face of moisture stress.
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Residential garden ponds contribute significantly to the available aquatic habitat within urban landscapes. Although garden ponds have novel biotic and abiotic characteristics, they are used by a variety of wildlife. However, whether they support healthy animals, reproduction and recruitment, critical for longer-term sustainability, is largely unknown. We addressed this knowledge gap using frogs as a case study taxon by investigating species assemblage, size (snout-vent length, SVL), body condition (scaled mass index, SMI), reproduction and recruitment in urban gardens with ponds relative to natural wetlands in southwestern Australia. Based on monthly sampling of 21 urban gardens and 6 wetlands between September 2023 and March 2024, we found that gardens supported a less diverse species assemblage than wetlands. Garden frogs were up to 39.5% longer in SVL but did not differ in SMI to those in wetlands. Of species occurring in both habitats, 75% (3) called earlier and/or for longer in gardens compared to wetlands. Over 40% of garden ponds supported reproduction of motorbike frogs (Litoria moorei) and of these 45% supported recently metamorphosed juveniles. Reproduction of the other species in gardens was minimal. This study is one of few to investigate the ability of urban habitats to support critical aspects of life history and demonstrates that residential garden ponds can sustain healthy adults, reproduction and recruitment for some species.
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Urbanization often changes bird species richness and affects the functional diversity. Therefore, understanding these changes helps city planners improve green space design and land use planning. Our study used multiple datasets to explore the effects of landscape patterns and natural environments on the functional diversity of birds in urban parks and campuses in the eastern and northwestern regions of China. Firstly, we used the data to calculate birds of the functional richness (FRic), functional evenness (FEve), and functional divergence (FDiv) of 68 urban spaces in the eastern and northwestern regions of China. Further, we established generalized linear models of natural factors, human factors, and functional diversity. Results showed more bird species with unique traits were in the northwestern region. This may be because the earlier urbanization in the eastern region filtered out urban-sensitive species, leaving behind urban adapters. Moreover, we found that the fractal dimension index was the most significant positive factor of FRic in the eastern region but the most significant negative factor of FDiv. Elevation was the most significant negative influence factor of FEve in the eastern region, but it was the most potent positive influence factor of FRic in the northwestern region. Population density had a significant positive effect on FDiv in the northwestern region. However, green space areas significantly negatively impacted FEve in the northwestern region. In addition, birds in parks in both regions had more functional traits than those on campuses, possibly because of the larger green space in parks, which may contain more fragments of native vegetation and reduce human interference. Our study suggests that preserving more original vegetation and reducing human disturbance in cities can increase the functional diversity of urban birds and improve urban ecosystem functions.
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The purpose of this study was to create hedges in the Biological Sciences department of Obafemi Awolowo University by utilizing decorative and potted plants to enhance the area’s visual appeal and practicality. Hedge were planted to stabilize and uphold the previously constructed walkway in order to produce a more picturesque landscape. The blooms in the Botany Department’s potted plants were rearranged, decorated, and given identification tags. The hedges were cultivated using cutting method with Duranta erecta, Polyscias scutellaria, Acalypha wilkesiania planted in the garden to beautify the area. Polyscias scutellaria was selected for the walkway border. The potted plant grown in this study were: Tradescantia spathacea, Cordyline fruticosa, Dieffenbachia seguine, Euphorbia milii, Dieffenbachia seguine, Euphorbia milii, Sansevieria hyacinthoides, Crinum americanum, Tradescantia pallida, Cuphea hyssopifolia, Syngonium auritum, Dracaena fragrans, Cheilocostus speciosus, Dieffenbachia seguine, Nephrolepsis biserrata, Dracaena fragrans, and Adiantum-capillus veneris. In conclusion, there is little doubt that the plant species chosen for this study will be useful for landscape architects and landscape environmental design. The biological buildings are even more gorgeous due to the aromatic flowers and lovely leaves of the plants. People at the Department will also benefit from the environmental advantages that the department’s potted plants have to offerr.
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Domestic (ȁ8privateȁ9) gardens constitute a substantial proportion of ȁ8green spaceȁ9 in urban areas and hence are of potential significance for the maintenance of biodiversity in such areas. However, the size and nature of this resource and its associated features are poorly known. In this study, we provide the first detailed audit, using domestic gardens in the city of Sheffield as a model study system. Domestic gardens, the mean area of which was 151 m2, cover approximately 33 km2 or 23% of the predominantly urban area of the city. The smaller gardens contribute disproportionately to this total because, although individually they add little, they are large in number. Conversely, the regions of the city with proportionately more garden area contribute most to the total garden area of the city, although such regions are limited in number. Based on the findings of a telephone based survey, 14.4% of dwellings with gardens were estimated to have ponds, 26% to have nest-boxes, 29% to have compost heaps, 48% to hold trees more than 3 m tall, and 14% of dwellings were estimated to be home to one or more cats. Whilst the absolute frequency of these features is low to moderate, by extrapolation they nonetheless yield estimates for domestic gardens in Sheffield of a total of 25,200 ponds, 45,500 nest boxes, 50,750 compost heaps, 360,000 trees, and a population of 52,000 domestic cats. These results are considered in the context of the role of gardens in urban areas as habitats for wildlife and the implications for housing policy.
Chapter
Domestic gardens associated with residential zones form a major component of undeveloped land in towns and cities. Such gardens may play a vital role in maintaining biodiversity in urban areas, but explanations for the variation in the richness of species assemblages in gardens are lacking. We report the results from a case study of 12 invertebrate groups in 61 domestic gardens in the city of Sheffield, UK. The mean number of species within a taxon, recorded per garden, was no greater than 3, 10, and 20 species in litter, pitfall trap and Malaise trap samples, respectively. Relatively speciose groups exhibited high turnover between gardens, with typically 50% of the group occurring only once. In contrast, several species-poor taxa were virtually ubiquitous. Species richness was analysed by multiple regression and hierarchical tree analysis in relation to garden and landscape variables. In general, the two methods of analysis corroborated one another. In total, 22 explanatory variables entered into regression models, although 12 of them only did so once. The amount of variation in species richness explained in models was generally quite high, with the factors involved operating over a range of scales. However, the patterns that emerged were not consistent across taxa. The most important predictors of species richness, of relevance to land use planners, were components of garden vegetation, especially the abundance of trees. Likely reasons for inconsistencies in the relationships are discussed in the context of sampling and species biology.
Chapter
Since the formation of the British Butterfly Conservation Society (BC) in 1968 the attitude of the average gardener to wildlife in the garden has changed considerably. In particular, many gardeners are now actively trying to attract butterflies into their gardens and many books have been published giving advice on ways to do this (e.g. Cribb, 1982; Rothschild and Farrell, 1983; Killingbeck, 1985; Oates, 1985; Payne, 1987), most being based on the authors’ own experiences.
Chapter
Some authors consider cities as ecosystems of a singular type (Meier 1976; Halffter et al. 1977). Their climate generally differs from that of the surrounding areas (Landsberg 1981; Miess 1979) and their functioning differs from natural processes (Wolman 1965). Humans are accompanied by a rich urban flora and fauna, composed mainly of species introduced voluntarily, such as ornamental and utilitarian plants, mammals, birds, reptiles, fish, and other taxa, or involuntarily, such as weeds, pathogens, and animal pests. Other anthropophilous native vertebrates, invertebrates, and plants can be added to the list. The anthropization process involves a series of adaptations to peculiarities of rural and urban environments (Falifiski 1968; Trojan 1982; Kowarik 1990).