Skip to main content
Browse Subject Areas

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Influence of Urbanization on Body Size, Condition, and Physiology in an Urban Exploiter: A Multi-Component Approach

  • Alizée Meillère ,

    Affiliation Centre d’Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Université de La Rochelle, Villiers-en-Bois, France

  • François Brischoux,

    Affiliation Centre d’Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Université de La Rochelle, Villiers-en-Bois, France

  • Charline Parenteau,

    Affiliation Centre d’Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Université de La Rochelle, Villiers-en-Bois, France

  • Frédéric Angelier

    Affiliation Centre d’Etudes Biologiques de Chizé (CEBC), UMR 7372 CNRS-Université de La Rochelle, Villiers-en-Bois, France


Consistent expanding urbanization dramatically transforms natural habitats and exposes organisms to novel environmental challenges, often leading to reduced species richness and diversity in cities. However, it remains unclear how individuals are affected by the urban environment and how they can or cannot adjust to the specific characteristics of urban life (e.g. food availability). In this study, we used an integrative multi-component approach to investigate the effects of urbanization on the nutritional status of house sparrows (Passer domesticus). We assessed several morphological and physiological indices of body condition in both juveniles (early post-fledging) and breeding adults from four sites with different levels of urbanization in France, Western Europe. We found that sparrows in more urbanized habitats have reduced body size and body mass compared to their rural conspecifics. However, we did not find any consistent differences in a number of complementary indices of condition (scaled mass index, muscle score, hematocrit, baseline and stress-induced corticosterone levels) between urban and rural birds, indicating that urban sparrows may not be suffering nutritional stress. Our results suggest that the urban environment is unlikely to energetically constrain adult sparrows, although other urban-related variables may constrain them. On the other hand, we found significant difference in juvenile fat scores, suggesting that food types provided to young sparrows differed highly between habitats. In addition to the observed smaller size of urban sparrows, these results suggest that the urban environment is inadequate to satisfy early-life sparrows’ nutritional requirements, growth, and development. The urban environment may therefore have life-long consequences for developing birds.


Pressures that human activities exert on the environment are steadily increasing and substantially affect ecosystem function [1]. In particular, consistent expanding urbanization irreversibly transforms the structure and ecological processes of natural habitats [2,3]. While some species seem to benefit from the urban environment (“urban exploiters”), many others seem unable to persist in cities (“urban avoiders”), and as a result, species richness and diversity overall is low in urban areas, especially for avian communities [36]. Indeed, urbanization exposes organisms to novel environmental challenges because of the specific characteristics of urban environments (e.g., resource availability, micro-climate, species interactions, disturbances, pollution; [713]). While the impact of urbanization on communities has been well documented [36,14,15], the mechanisms underlying organisms’ responses to urbanization are still poorly understood [8,16,17]. Yet, the modified environmental conditions of urban environments expose organisms to new selective pressures that are likely to affect wild vertebrates. For instance, studies have reported differences in behavior, morphology, and physiology between urban and non-urban populations (e.g., [1823]) in a large range of species. Because the ability to successfully adapt to urban-related environmental changes can vary with species’ ecological and life history traits (e.g., dispersal ability, behavioral flexibility, diet, stress tolerance, annual fecundity [15,24,25]), organisms’ responses to urbanization differ highly among species. In a rapidly urbanizing world, it is crucial to understand not only how free-living organisms are affected by the urban environment, but also how they can or cannot adjust to its constraints.

Among other factors, food availability can be dramatically modified in cities [2,26,27]. Food types, quantity, and predictability certainly differ between rural and urban areas, and this is likely to have huge effect on individual fitness because energetic status is known to affect survival, reproductive performance, and the development of wild vertebrates [2830]. However, the ultimate consequences of urban food resources on free-living organisms remain subject to debate [3032]. First, food availability and predictability can be increased in cities compared to natural habitats because of human activities that consistently provide reliable food year-round [26]. Therefore, one could expect urban vertebrates to benefit from their environment and to be in overall good body condition (i.e., energetic state of an individual). Second, high food predictability could counter-intuitively have the opposite influence on body condition. Accumulating body reserves serves as a buffer against unpredictable temporary food shortage in birds [33,34], but is also associated with important metabolic and/or locomotory costs [35,36]. Therefore, individuals are predicted to reduce their body mass when living in a highly predictable environment where food shortages are scarce (i.e., adaptive mass regulation; reviewed in [37]), such as urban environments. Finally, although food quantity may not be impoverished in cities, high urban avian density could lead to strong inter-individual competition, and therefore, to poor food availability, overall [26,38]. In addition, urban wild vertebrates might rely on human-provided food (e.g., birdseed, refuse) because natural food is limited in terms of quantity and quality in cities [3941]. Such food sources may be of insufficient quality and might not cover all nutritional requirements of urban wild vertebrates, especially during critical life-history stages (e.g., nestling or juvenile stages) or costly life-history events (e.g., reproduction) [27]. For these reasons, an urban diet may be insufficient to sustain energetic demands, therefore leading to poor body condition in urban individuals.

Because the same body condition pattern can result from different causes, assessing the exact energetic situation of urban wild vertebrates is challenging. To disentangle all these hypotheses, it is necessary to measure complementary indices of body condition. In addition to classical morphometric indices [42,43], further proxies for condition should be used, such as fat and pectoralis muscle scores [4446]. These scores can aid in understanding whether differences in body condition are associated with energetic constraints or with an adaptive reduction of body mass [47,48]. Individuals are predicted to maintain their muscle mass and to preferentially reduce their fat stores when reducing their body mass for adaptive purposes, such as migration or reproduction [49,50]. However, both fat and muscle stores are predicted to decline when individuals become energetically constrained [49,51]. Because of the determinate growth of some vertebrates (e.g., birds, mammals), morphological measures are also crucial to consider when assessing the energetic situation of developing individuals [52]. Finally, other physiological indices can also be useful to understand the impact of specific environmental conditions on individual energetic status [16,22,53,54]. For instance, hematocrit is known to vary with energetic demands [55], and low hematocrit is also thought to be associated with survival costs in birds [56,57]. Therefore, low hematocrit could be an indicator of poor health status [55,58], and as a consequence, could provide a useful indicator of potential energetic constraints in urban birds. Likewise, corticosterone (hereafter CORT, the primary avian stress hormone) is an important mediator of allostasis, and CORT levels and the adrenocortical stress response are strongly related to the energetic status of an organism [59,60]. Thus, fasting usually triggers CORT secretion [6165] whereas food intake is associated with a reduction of CORT levels [66,67]. Interestingly, the relationship between CORT levels and body condition is non-linear and CORT levels dramatically increase only when individuals reach a low condition threshold that is associated with nutritional stress [61,68]. Indeed, baseline (i.e., CORT levels in the absence of acute stressful events) and stress-induced CORT levels are known to increase when individuals are fed with food that does not allow sustaining their nutritional needs either quantitatively or qualitatively [69,70]. Moreover, elevated CORT levels are often associated with an increased risk of mortality [68,7173]. Consequently, CORT levels can be a relevant addition to body condition when assessing the nutritional status of individuals [72,74].

To date, most studies have focused only on a limited number of body condition indices, a limited number of sites, a small sample size, and/or a single life-history stage, therefore making it difficult to fully assess the impact of urbanization on the nutritional status of wild vertebrates (but see [53]). Some studies have reported that urban individuals are in poorer condition than rural ones [7580], but others have not found this difference [53,77]. The results regarding physiological indices of individual energetic condition are likewise inconsistent [16,19,23,53,8190]. Because of these discrepancies, it remains difficult to determine whether urban birds are constrained by their environment or not. The house sparrow (Passer domesticus) is among the best examples of “urban exploiter” species, and is particularly well suited to investigate this question. Although certainly one of the most successful birds in the urban environment, the house sparrow has undergone population declines in the last several decades, particularly in European cities [91,92] and recent studies have suggested that poor food conditions may be one of the drivers of these declines [53,78,93]. Studies assessing the impact of urbanization on sparrows’ condition have shown that urban adult sparrows are generally in poorer condition than rural ones during the non-breeding season [7779]. However, these results are not entirely supported by a more recent study [53], that reported no negative effect of urbanization in adult house sparrows. Similarly, studies investigating the influence of urbanization on CORT levels have also found conflicting patterns [53,84,94]. Furthermore, the constraints of urban life are likely to primarily affect individuals during critical life-history stages (e.g., early post-fledging period) and/or during costly stages of the annual cycle (e.g., reproduction), but to date, these periods have been overlooked. Because of the inconsistency of findings, it seems particularly important to investigate whether similar patterns are observed in other geographic locations, and also during constraining life-history stages.

In this study, we investigated the impact of urbanization on the nutritional status of free-living house sparrows using an integrative multi-component approach. We measured several morphological, hematological and hormonal indices of body condition in four populations of house sparrows (Passer domesticus), from sites with different levels of urbanization in France, Western Europe. We focused on both juveniles (i.e., young that have fledged during that season, before their first molt) and breeding adults to understand whether the impact of urbanization on wild birds is especially apparent during the post-fledging period (when the birds are inexperienced) and the reproductive period (when energetic demands are increased) [46]. By monitoring complementary and relevant characteristics of adults and juveniles from four sites, we will test whether house sparrows benefit from the urban environment (hypothesis 1), are constrained by the urban environment (hypothesis 2), adaptively reduced their body mass because of predictable urban food availability (hypothesis 3), and if the observed pattern differs between life-history stages. As explained earlier, each of these non-mutually exclusive hypotheses should be associated with specific patterns regarding our variables of interest (Table 1).

Table 1. Predicted response of morphological and physiological variables according to the different hypotheses of the impact of urbanization on the nutritional status of free-living house sparrows.

Materials and Methods

Ethics statement

This study was carried out in accordance with all applicable institutional and/or national guidelines for the care and use of animals. All experimental procedures were approved by the “Comité d’Ethique en Expérimentation Animale Poitou-Charentes”, France (authorization number: CE2012-7). Permits for the capture, sampling and banding of house sparrows were issued by the “Centre de Recherches sur la Biologie des Populations d’Oiseaux” (permit numbers 15077 and 13794 delivered respectively to AM and FA). When sampling occurred on public land (2 sites: CEBC and La Rochelle, see below), permission was granted by the responsible authorities, i.e. the “Préfecture de la Charente-Maritime”, the “Préfecture des Deux-Sèvres”, and the “Centre d’Etudes Biologiques de Chizé”. Capture of sparrows on private property (2 sites: Niort and Villefollet, see below) was carried out with the land owners’ specific permission.

Study species and sites

During the breeding season 2013, we captured 110 house sparrows (68 adults and 42 juveniles) with mist-nets at four sites in Western France (two urban and two rural sites, Table 2). The two urban sites are located within two medium-sized cities (La Rochelle, 46°08’52.8”N, 1°09’12.7”W, 75,000 inhabitants, and Niort, 46°18’46.4”N, 0°28’44.3”W, 58,000 inhabitants) whereas the two rural sites are situated in sparsely populated areas, surrounded by agricultural areas (in the village of Villefollet, 46°07’37.7”N, 0°16’04.4”W, 200 inhabitants) or by forests (at the Centre d’Etudes Biologiques de Chizé—hereafter CEBC, 46°08′50.5”N, 0°25′34.2”W, ~100 inhabitants). To quantify the degree of urbanization at each capture site, we followed the method developed by [78] for house sparrows. Briefly, we used digital aerial photographs (GoogleMaps) of 1 km x 1 km areas around each capture site that we divided into 100 cells. We extracted five habitat characteristics: mean building density score, number of cells with high building density, number of cells with road, mean vegetation density score, and number of cells with high vegetation density (Table 2). We then calculated an “urbanization score” for each site using the PC1 value from a principal component analysis on the five habitat variables (Table 2). The PC1 accounted for 91.2% of the total variance and correlated positively with artificial surfaces (building and roads) and negatively with vegetation cover.

Table 2. Habitat characteristics of the capture sites and sample sizes.

Bird sampling

Adult and juvenile sparrows were captured by “permanently monitored passive netting” as detailed in [95]. Sparrows were aged as adult or juvenile based on plumage characteristics [96]. Each capture site was sampled weekly: adults were captured from May 13 to August 11 and juveniles from June 16 to August 23. Capture dates did not differ between sites (ANOVA: adults: F3,64 = 2.147, p = 0.103; juveniles: F3,38 = 0.642, p = 0.593). The sample size for each site is summarized in Table 2.

In order to quantify baseline CORT concentrations, birds must be sampled within 3 min of capture [95,97]. We thus monitored the mist-nets permanently until a bird was captured. Immediately after capture, the bird was extracted from the mist-net and blood sampled as quickly as possible (mean ± SE: 2 min 39 sec ± 2 sec; range: 1 min 13 sec—3 min 45 sec). Blood samples were collected from the alar vein using a 27-gauge needle and heparanized microcapillary tubes (up to 150 μL for CORT assay and 10 μL for hematocrit measurement). CORT levels measured at the first blood sampling were not related to handling time (r = 0.008, p = 0.714, n = 110), and were therefore considered to be representative of “baseline CORT” levels. To measure the stress response, the bird was then kept in a cloth bag and a second blood sample was collected after 30 min (standard capture/restraint stress protocol; [98]). This second sample reflects the maximum CORT level (“stress-induced CORT”). Finally, the bird was banded with a numbered metal ring, weighed, measured (see below for details), and released at its site of capture.

Morphological and hematocrit measurements

All birds were weighed (electronic balance: ± 0.1 g), and their wing length (steel rule: ± 1 mm) and tarsus lengths (caliper: ± 0.1 mm) were measured. For consistency and to avoid potential methodological bias, morphological and hematocrit measurements were all collected by AM. The repeatability of the morphological measurements was very high (intra-class correlation coefficient R: tarsus length: R = 0.963; wing length: R = 0.999; n = 17). Additionally, we recorded fat and muscle scores as detailed in [4446]. To assess birds’ body condition, we used the “scaled mass index” (hereafter SMI) as recommended by [99,100]. The SMI adjust the mass of all individuals to that expected if they had the same body size [99]. We used tarsus length to calculate the SMI because it best correlated with body mass (tarsus length: r = 0.444, p < 0.001; wing length: r = 0.289, p < 0.001). The relationship between body mass and tarsus length was similar for males and females (Likelihood ratio = 1.751, p = 0.186) but different for adults and juveniles (Likelihood ratio = 9.039, p = 0.003), thus the SMI was calculated separately for adults and juveniles. The SMI was computed for each i individual as follows: where Mi and Li are, respectively, the body mass and the tarsus length of the individual i, L0, the arithmetic mean value of tarsus length for the whole study population (adults: L0 = 18.76 mm, n = 68; juveniles: L0 = 18.11 mm, n = 42) and b the slope estimate of a standardized major axis (SMA) regression of log-transformed body mass on log-transformed tarsus length (adults: b = 1.35; juveniles: b = 2.20). Finally, we also measured hematocrit levels as an indicator of condition and health status [55,58]. Hematocrit was determined by centrifuging blood in a microcapillary tube (11000 rpm, 3min): the volume of red blood cells was expressed as a percentage of the total blood volume.

Molecular sexing and hormone assay

Blood samples were centrifuged (4500 rpm, 7min), and plasma and red blood cells were separated and stored at -20°C until analyzed. Adult house sparrows were sexed visually (plumage characteristics; [96]), but the sex of juveniles was determined by molecular sexing as detailed in [101]. Plasma concentrations of CORT were measured in duplicate by radio-immunoassay, as previously described [102]. The minimum detectable CORT level was 0.83 ng.mL-1, and the intra- and inter-assay coefficients of variation were 7.07% and 9.99% respectively. All laboratory analyses were performed at the Centre d’Etudes Biologiques de Chizé (CEBC).

Data analysis

All statistical analyses were performed in R 3.1.0 [103]. First, we fitted general linear models (GLMs; normal errors and identity link function) to test whether body size and condition differed between capture sites (response variables: tarsus length, wing length, body mass, SMI, fat score or muscle score). We used “site” (four-level factor from least to most urbanized: CEBC, Villefollet, Niort and La Rochelle) as explanatory variable, and included “age” (two-level factor: adult and juvenile; except for SMI where adults and juveniles were analyzed separately) and “sex” (two-level factor: male and female), as covariates. Each full model also included all 2-way interactions. For body mass and SMI analyses, we also included “time” of day as a covariate. Second, we fitted GLMs with normal errors and identity link function to determine whether physiological parameters differed between capture sites (response variable: baseline CORT, stress-induced CORT or hematocrit levels). Each full model included site, age, sex, and time of day (and a squared term: “time²” for the CORT models) and all 2-way interactions between site, age and sex. Baseline and stress-induced CORT levels were log10-transformed to ensure the normality of model residuals, but we present non-transformed values to facilitate interpretation. We did not include the “capture date” in the analyses because this variable differed highly between age classes and including age and capture date in the same models could lead to biased results (i.e. multicollinearity; [104]). Importantly, capture dates did not differ between sites (ANOVA, all p > 0.103, see above for details).

We performed all our model selection using a stepwise approach starting from the full model including all the independent variables and interactions. We used likelihood ratio test and removed non-significant factors and covariates one at a time until we reached the most parsimonious model. Tukey’s HSD (Honest Significant Difference) post-hoc tests were used to conduct pairwise comparisons between capture sites. All models were checked for assumptions of equal variances and normality of residuals.


Body size and condition

Both tarsus and wing lengths were significantly longer in adults than in juveniles (Table 3A and 3B, Fig 1A), and wing length was also significantly longer in males than in females, for adults only (Table 3B). Body mass also differed between age classes (Table 3C, Fig 1B), with adults being significantly heavier than juveniles. Wing length was not affected by the capture site (GLM: F3,101 = 0.860, p = 0.465), and the “site × sex” (F3,97 = 0.931, p = 0.429) or “site × age” (F3,100 = 2.140, p = 0.100) interactions. However, tarsus length and body mass significantly differed between sites (Table 3A and 3C), with sparrows from urban sites (Niort and La Rochelle) being generally smaller and lighter than rural ones (CEBC and Villefollet). Specifically, for all significant pairwise comparisons between sites, sparrows captured in more urbanized sites had smaller tarsus and weighed less than those captured in less urbanized sites (Fig 1A and 1B). Moreover, the “site × age” and “site × sex” interactions were not significant, suggesting that the influence of capture site on tarsus length and body mass did not significantly differ between adults and juveniles (tarsus: F3,98 = 0.746, p = 0.526; body mass: F3,97 = 0.756, p = 0.522) or males and females (tarsus: F3,101 = 0.908, p = 0.440; body mass: F3,100 = 1.464, p = 0.229).

Fig 1. Mean ± SE (A) tarsus lengths and (B) body mass of sparrows captured in 4 sites with different levels of urbanization.

Sites are ordered from least to most urbanized (PC1 values) with two rural (CEBC and Villefollet) and two urban sites. Filled circles represent adults and open circles represent juveniles (n = 110, see Table 2 for details). Differing letters indicate statistical difference between sites for both adults and juveniles (Tukey’s HSD test).

Table 3. Minimum adequate models when investigating the influence of capture site on several morphological parameters.

The SMI did not significantly differ between sites for both adults (GLM: F3,63 = 0.237, p = 0.870, Fig 2A) and juveniles (GLM: F3,37 = 0.624, p = 0.604, Fig 2B). Moreover, the SMI was not affected by sex or time of day (all p > 0.307 for both age classes).

Fig 2. Mean ± SE scaled mass index values of (A) adult and (B) juvenile sparrows captured in 4 sites with different levels of urbanization.

Sites are ordered from least to most urbanized (PC1 values) with two rural (CEBC and Villefollet) and two urban sites. Filled circles represent adults and open circles represent juveniles (n = 110, see Table 2 for details). The SMI did not significantly differ between sites as indicated by the similar letters (Tukey’s HSD test).

Adults had significantly lower fat score than juveniles (Table 3D) and higher muscle score than juveniles in males but not in females (Table 3E). There was an effect of the “site × age” interaction on fat score (Table 3D). Specifically, fat score significantly differed between sites in juveniles only, with sparrows captured in the less urbanized site (CEBC) having lower fat score than those captured in the two urban sites (Niort and La Rochelle, Fig 3A). Juveniles captured in Villefollet (rural) also had lower fat scores than those captured in Niort and La Rochelle (urban) but the differences were marginally significant (Tukey’s HSD test: Villefollet vs. Niort: p = 0.067; Villefollet vs. La Rochelle, p = 0.103). Finally, the site of capture had a significant effect on muscle score (Table 3E), but the observed differences were independent of urbanization: sparrows captured in Niort had lower muscle score than sparrows captured in the three other sites (Fig 3B).

Fig 3. Mean ± SE (A) fat and (B) muscle scores of sparrows captured in 4 sites with different levels of urbanization.

Sites are ordered from least to most urbanized (PC1 values) with two rural (CEBC and Villefollet) and two urban sites. Filled circles represent adults and open circles represent juveniles (n = 110, see Table 2 for details). Differing letters indicate statistical difference between sites for juveniles only (A) or for both adults and juveniles (B) (Tukey’s HSD test).

Physiological parameters

Baseline CORT levels did not significantly differ between capture sites (F3,103 = 0.273, p = 0.845, Fig 4A) and were not affected by sex (F1,102 = 0.378, p = 0.540), and the “site × sex” (F3,98 = 0.293, p = 0.831) or “site × age” (F3,95 = 0.153, p = 0.927) interactions. However, baseline CORT levels were significantly lower in juveniles than in adults (Table 4A, Fig 4A).

Fig 4. Mean ± SE (A) baseline and (B) stress-induced CORT levels of sparrows captured in 4 sites with different levels of urbanization.

Sites are ordered from least to most urbanized (PC1 values) with two rural (CEBC and Villefollet) and two urban sites. Filled circles represent adults and open circles represent juveniles (n = 110, see Table 2 for details). Differing letters indicate statistical difference between sites for both adults and juveniles (Tukey’s HSD test).

Table 4. Minimum adequate models when investigating the influence of capture site on several physiological parameters.

Site, age, and sex had a significant effect on stress-induced CORT levels (Table 4B). Stress-induced CORT levels were significantly lower in juveniles than in adults (Fig 4B), and lower in males than in females. Stress-induced CORT levels also significantly differed between capture sites (Table 4B), but the observed differences were not related to urbanization (Fig 4B). Specifically, stress induced CORT levels were significantly higher in one rural site (CEBC) than in the other rural site (Villefollet) and one urban site (Niort) and were significantly different between the two urban sites (lower in Niort than in La Rochelle; Fig 4B). Moreover, the “site × age” and “site × sex” interactions were not significant, suggesting that the influence of capture site on stress-induced CORT levels did not significantly differ between adults and juveniles (F3,95 = 0.440, p = 0.725) or males and females (F3,98 = 0.631, p = 0.597).

Hematocrit levels did not significantly differ between capture sites (F3,104 = 1.010, p = 0.391) and were not affected by sex (F1,103 = 0.008, p = 0.928) and the “site × sex” (F3,100 = 1.146, p = 0.800) or “site × age” (F3,97 = 0.461, p = 0.710) interactions. However, hematocrit levels significantly differed between age classes (Table 4C), with juveniles having a lower hematocrit than adults.


Impact of urbanization on condition

In our study, we did not detect any evidence of an effect of urbanization on the SMI of both adults and juveniles, indicating that body condition of sparrows did not differ between urban and rural areas during these two critical stages (early post-fledging and breeding periods). Thus, despite the urban decline of some populations, the house sparrow does not seem to be particularly energetically constrained by the urban environment. Our results complement and are in accordance with another recent study that examined the influence of urbanization on the condition of house sparrows during other stages of the annual cycle in Hungary [53]. On the other hand, these results are not supported by other studies [78,79], which reported that urban sparrows are generally in poorer condition relative to their rural conspecifics. However, the conclusions of these studies were based on a condition index computed using mass-length residuals, a method that have recently been subject to debate [53,99,100]. In addition to the SMI, we also investigated complementary indices of body condition (i.e., fat and muscle scores, wing length, and several physiological indices) that all led to the same conclusion, strongly suggesting that urban sparrows are not suffering from nutritional stress. First, we did not find any consistent differences in fat and muscle scores between urban and rural adult sparrows, suggesting that urban adult sparrows were probably not energetically constrained [49,51]. Second, wing length did not differ between sites, thus, urban sparrows did not appear to face particularly important energetic constraints at the time of feather growth [105]. Third, we did not find any difference in hematocrit levels between urban and rural house sparrows, suggesting that urban sparrows did not suffer from anemia [55,58]. Finally, we did not detect any significant and clear effect of urbanization on baseline or stress-induced CORT levels, suggesting that urban sparrows are not energetically stressed [6165,70]. Altogether, our results support the conclusion that urban sparrows are unlikely to be energetically constrained by the urban environment or to have adaptively reduced their body mass because of high food predictability in cities (rejecting hypothesis 2 and 3; Table 1).

Although we did not find any evidence suggesting that the urban nutritional environment affects house sparrows’ body condition, studies conducted on other species have reported that urban individuals are in poorer (e.g., Rufous-collared sparrow, Zonotrichia capensis [75]), similar (e.g., House Finch, Haemorhous mexicanus [87]) or better (e.g., Northern mockingbird, Mimus polyglottos [77]) condition compared to their rural conspecifics. These discrepancies highlight the contrasting abilities of different species to cope with the specific characteristics of urban environments. “Urban exploiter” species are expected to be in good body condition, as they might be better able to exploit urban food resources. However, in the present study, the house sparrow does not seem to benefit to a large extent from living in cities (rejecting hypothesis 1; Table 1), as urban sparrows were not in better condition relative to rural ones, and this idea is further supported by the recent decline of this species in European urban areas [91,92,106].

Impact of urbanization on morphology

Although our study supports the idea that adult and juvenile house sparrows do not suffer from urbanization in term of body condition, we found large and significant differences in tarsus length along the urbanization gradient. Specifically, urban sparrows were smaller than their rural conspecifics and this finding is supported by other studies on house sparrow populations [53,78,79], and other bird species (e.g., [107]). However, a recent study investigating the effect of urbanization on avian morphology using paired urban and rural populations of European blackbirds (Turdus merula) along a latitudinal gradient, reported inconsistent (i.e., locality-dependent) difference between urban and rural populations [108]. In our study, sparrows captured in more urbanized sites had consistently smaller tarsi and weighed less than those captured in less urbanized sites. However, for one pairwise comparison there was a tendency for similar tarsus length between one urban and one rural site (NIORT vs. CEBC, see Fig 1), mostly because of the small size of juveniles captured at the CEBC. Here, it is important to acknowledge that our sample size was moderate for juveniles (42 juveniles), which could have limited our ability to detect an effect of urbanization and could explain the lack of difference between the two sites. However, this could also suggest that despite a strong effect of urbanization on sparrows’ morphology, this effect can be reduced or accentuated because of local specific characteristics of each site. Our results also highlight the importance of investigating more than one urban and one rural population to fully assess the influence of urbanization on wild vertebrates.

Interestingly, tarsus lengths differed among our studied populations, while wing lengths were similar. In house sparrows, the tarsus is almost fully grown at fledging, whereas wing length is mainly determined by the length of primary feathers that are replaced every year (post-nuptial molt) and a few weeks after fledging (the post-fledging molt) [96]. Thus, the smaller tarsi of urban birds probably results from energetic constraints on developing nestlings or fledglings. Several hypotheses could explain the production of smaller individuals in cities. First, it may arise from parents’ reproductive decisions (e.g., trade-offs between clutch size and nestlings’ body condition; [26]), but this seems unlikely in house sparrows because clutch sizes (a proxy for parental investment) have been shown to be similar in urban and rural habitats [109]. Second, the urban environment could constrain nestling development through, for example, a direct effect of low quality, low quantity, or contaminated food on growth [93,110], but also through a potential indirect effect of urban noise on the parental provisioning of the brood [111]. Finally, the smaller body size of urban birds may also result from adaptive divergences between urban and rural populations. For instance, differences in predator regime (e.g., strong predation in cities; [78,112]), micro-climate (e.g., urban heat island effect and Bergman’s rule; [108,113]) and/or migration tendencies (e.g., reduced migratory tendencies in cities and Seebohm’s rule; [108,114]) may favor individuals of smaller body size in urban environments. However, most of these hypotheses seem unlikely in house sparrows as we did not find evidence for smaller wing length in urban individuals, and further investigations would be needed to assess differences in predation pressure between urban and rural sites.

In addition to the smaller size of urban sparrows, we found significant differences in juvenile fat scores between capture sites, with urban juveniles having, surprisingly, higher fat scores than rural ones. These results could suggest that food types provided to nestlings and juveniles highly differed between urban and rural habitats. The difference in body reserves between urban and rural juveniles could thus indicate that urban sparrows might not feed their nestlings and young fledglings with arthropod prey only (i.e., the main component of nestling sparrows’ diet; [96]) because this type of food is less available in the urban environment [115]. Instead, they may incorporate fatter and highly accessible human-provided food in their diets [39,93,116]. Because such food could be inadequate or of insufficient quality (e.g., lower protein or calcium content) to satisfy all nestlings’ nutritional requirements, this may have negatively affected their growth and development [27,39,116]. Accordingly, Seress et al. (2012) reported that suburban house sparrows produce smaller fledglings than their rural conspecific in Central Europe [93]. Moreover, the results from their common garden and cross-fostering experiments support the idea that these differences result from different nestling diets in urban and rural habitats [93]. Altogether, our results and these studies suggest that urban house sparrows are constrained by their environment during their developmental phase at a large European scale (supporting hypothesis 2 during development only, Table 1).

Urban environments differ highly from natural habitats [3,8], and most of urban-associated factors are likely to affect several traits, such as morphology, in wild vertebrates. For instance, habitat structure, pollution levels, and climate can influence urban arthropod communities [115,117], as well as, human presence contributes to anthropogenic provision of food resources in cities [3941]. As a result, divergences in diets, and associated developmental and morphological consequences, are likely to arise as a result of urbanization. Because conditions experienced during development influence phenotypic development and can shape individual life histories [52,118], the smaller body size in urban populations may have important consequences for fitness, and ultimately for populations viability. A smaller body size is often related to poorer developmental conditions and to poorer performance (survival and reproductive success) later in life [52,107,119,120]. The concomitant smaller size and decline of urban house sparrow populations in Europe supports this hypothesis. However, a smaller body size can also be adaptive under some circumstances if it allows an individual to better perform in its environment (reviewed in [121]). Since contradictory hypotheses can explain the smaller size of urban individuals, further investigations are needed to better assess whether smaller structural size in urban populations might be adaptive or might lead to important fitness costs.

Impact of urbanization on stress physiology

We did not detect any evidence of an effect of urbanization on stress physiology, suggesting therefore that urban sparrows do not experience intense nutritional stress relative to rural sparrows. However, we found significant and large differences in the stress response between sites independently of the degree of urbanization, suggesting that the relationship between stress physiology and urbanization is complex and inconsistent. Accordingly, to date, no general and clear patterns have been revealed regarding the stress physiology of urban birds (reviewed in [16]). Studies have reported positive, negative and mainly null relationships between urbanization and stress-induced CORT levels (e.g., see [19,23,53,82,84,88,90]) and the observed effects not only differed among but also within species with differences depending on the sex, the life-history stage, or the year [16].

In addition to the energetic status, numerous intrinsic (e.g., sex, age, quality, reproductive status, species life history; [23,81,122124]) and/or extrinsic factors (e.g., weather, predation risk, noise, pollution; [125128]) can influence the CORT stress response and could have masked any general effect of urbanization on stress physiology [129]. Importantly, we found similar patterns of CORT secretion between sites for both breeding adults and juveniles indicating that breeding effort was not a confounding factor in our study [123]. Other studies have investigated the effects of urbanization on other measures of physiological stress (e.g., oxidative stress), and have also reported conflicting patterns (e.g. see [86,87]). Altogether, these studies highlight the importance of investigating multiple physiological components (e.g., oxidative stress, CORT stress response, parasite infection, carotenoid levels; [19,22,23,53,86,87,89,130]. Overall, the relationship between urbanization and avian stress physiology appears complex and the observed differences between sites are likely due to site-specific characteristics (e.g., parasites, pollution, predation) that may outweigh a potential effect of urbanization on these physiological components.


We found no evidence of an effect of urbanization on the condition of house sparrows during two energy-demanding stages (early post-fledging and breeding periods). By using an integrative multi-component approach, incorporating morphological, structural and physiological measures from both breeding adults and juveniles from four different sites, we also demonstrated that adult urban sparrows are not energetically constrained by the urban environment. Conversely, our results strongly suggest that the urban nutritional environment is inadequate or of insufficient quality to satisfy all nutritional requirements of developing sparrows, and therefore, that the urban environments are likely to energetically constrain free-living birds during their developmental phase only. However, the long-term consequences of growing in an urban environment remain unclear and future studies should explore these questions by comparing urban and rural populations [22,54]. More generally, the study of the consequences of urban life on wildlife may benefit from adopting experimental approaches (e.g., see [19,93,111,116,126]) to disentangle the relative importance of confounding factors (e.g., food quality versus predictability and/or quantity, urban noise, pollution, predation) on performances. These experimental studies will also help ecologists to assess the mechanisms underlying organismal responses to urbanization. Finally, they will also provide unequivocal evidence to explain the recent population trends—positive or negative—of some urban vertebrates.

Supporting Information


We are grateful to G. Gouchet, L. Sourisseau and D. Dion for their help in the field, to S. Ruault and C. Trouvé for molecular sexing and hormone assays, and to J.K. Grace for improving the English. We also thank Dr. Claudio Carere and 2 anonymous reviewers for their helpful comments and suggestions.

Author Contributions

Conceived and designed the experiments: AM FA FB. Performed the experiments: AM FA FB. Analyzed the data: AM. Contributed reagents/materials/analysis tools: AM FA FB CP. Wrote the paper: AM FA FB.


  1. 1. Vitousek PM, Mooney HA, Lubchenco J, Melillo JM. Human domination of Earth’s ecosystems. Science. 1997;277: 494–499.
  2. 2. Marzluff JM. Worldwide urbanization and its effects on birds. In: Marzluff JM, Bowman R, Donnelly R, editors. Avian Ecology and Conservation in an Urbanizing World. Norwell, Massachusetts: Kluwer Academic Publishers; 2001. pp. 19–47.
  3. 3. McKinney ML. Urbanization, biodiversity, and conservation. Bioscience. 2002;52: 883–890.
  4. 4. Blair RB. Land use and avian species diversity along an urban gradient. Ecol Appl. 1996;6: 506–519.
  5. 5. Chace JF, Walsh JJ. Urban effects on native avifauna: a review. Landsc Urban Plan. 2006;74: 46–69.
  6. 6. Clergeau P, Croci S, Jokimäki J, Kaisanlahti-Jokimäki M-L, Dinetti M. Avifauna homogenisation by urbanisation: analysis at different European latitudes. Biol Conserv. 2006;127: 336–344.
  7. 7. Gering JC, Blair RB. Predation on artificial bird nests along an urban gradient: predatory risk or relaxation in urban environments? Ecography. 1999;22: 532–541.
  8. 8. Shochat E, Warren PS, Faeth SH, McIntyre NE, Hope D. From patterns to emerging processes in mechanistic urban ecology. Trends Ecol Evol. 2006;21: 186–191. pmid:16701084
  9. 9. Grimm NB, Faeth SH, Golubiewski NE, Redman CL, Wu J, Bai X, et al. Global change and the ecology of cities. Science. 2008;319: 756–760. pmid:18258902
  10. 10. Schlesinger MD, Manley PN, Holyoak M. Distinguishing stressors acting on land bird communities in an urbanizing environment. Ecology. 2008;89: 2302–2314. pmid:18724740
  11. 11. Barber JR, Crooks KR, Fristrup KM. The costs of chronic noise exposure for terrestrial organisms. Trends Ecol Evol. 2010;25: 180–189. pmid:19762112
  12. 12. Kempenaers B, Borgstroem P, Loes P, Schlicht E, Valcu M. Artificial Night Lighting Affects Dawn Song, Extra-Pair Siring Success, and Lay Date in Songbirds. Curr Biol. 2010;20: 1735–1739. pmid:20850324
  13. 13. Bichet C, Scheifler R, Cøeurdassier M, Julliard R, Sorci G, Loiseau C. Urbanization, trace metal pollution, and malaria prevalence in the house sparrow. PLoS One. 2013;8: e53866. pmid:23342022
  14. 14. Croci S, Butet A, Georges A, Aguejdad R, Clergeau P. Small urban woodlands as biodiversity conservation hot-spot: a multi-taxon approach. Landsc Ecol. 2008;23: 1171–1186.
  15. 15. Hamer AJ, McDonnell MJ. The response of herpetofauna to urbanization: inferring patterns of persistence from wildlife databases. Austral Ecol. 2010;35: 568–580.
  16. 16. Bonier F. Hormones in the city: Endocrine ecology of urban birds. Horm Behav. 2012;61: 763–772. pmid:22507448
  17. 17. Sol D, Lapiedra O, González-Lagos C. Behavioural adjustments for a life in the city. Anim Behav. 2013;85: 1101–1112.
  18. 18. Rasner CA, Yeh P, Eggert LS, Hunt KE, Woodruff DS, Price TD. Genetic and morphological evolution following a founder event in the dark-eyed junco, Junco hyemalis thurberi. Mol Ecol. 2004;13: 671–681. pmid:14871370
  19. 19. Partecke J, Schwabl I, Gwinner E. Stress and the city: urbanization and its effects on the stress physiology in European blackbirds. Ecology. 2006;87: 1945–1952. pmid:16937632
  20. 20. Møller AP. Flight distance of urban birds, predation, and selection for urban life. Behav Ecol Sociobiol. 2008;63: 63–75.
  21. 21. Mccleery RA. Changes in fox squirrel anti-predator behaviors across the urban–rural gradient. Landsc Ecol. 2009;24: 483–493.
  22. 22. Møller AP, Erritzøe J, Karadas F. Levels of antioxidants in rural and urban birds and their consequences. Oecologia. 2010;163: 35–45. pmid:20012100
  23. 23. Lucas LD, French SS. Stress-induced tradeoffs in a free-living lizard across a variable landscape: consequences for individuals and populations. PLoS One. 2012;7: e49895. pmid:23185478
  24. 24. Møller AP. Successful city dwellers: a comparative study of the ecological characteristics of urban birds in the Western Palearctic. Oecologia. 2009;159: 849–858. pmid:19139922
  25. 25. Evans KL, Chamberlain DE, Hatchwell BJ, Gregory RD, Gaston KJ. What makes an urban bird? Glob Change Biol. 2011;17: 32–44.
  26. 26. Shochat E. Credit or debit? Resource input changes population dynamics of city-slicker birds. Oikos. 2004;106: 622–626.
  27. 27. Chamberlain DE, Cannon AR, Toms MP, Leech DI, Hatchwell BJ, Gaston KJ. Avian productivity in urban landscapes: a review and meta-analysis. Ibis. 2009;151: 1–18.
  28. 28. Wellicome TI, Danielle Todd L, Poulin RG, Holroyd GL, Fisher RJ. Comparing food limitation among three stages of nesting: supplementation experiments with the burrowing owl. Ecol Evol. 2013;3: 2684–2695. pmid:24567832
  29. 29. Perrig M, Grüebler MU, Keil H, Naef-Daenzer B. Experimental food supplementation affects the physical development, behaviour and survival of Little Owl Athene noctua nestlings. Ibis. 2014;156: 755–767.
  30. 30. Harrison TJ, Smith JA, Martin GR, Chamberlain DE, Bearhop S, Robb GN, et al. Does food supplementation really enhance productivity of breeding birds? Oecologia. 2010;164: 311–320. pmid:20473622
  31. 31. Plummer KE, Bearhop S, Leech DI, Chamberlain DE, Blount JD. Winter food provisioning reduces future breeding performance in a wild bird. Sci Rep. 2013;3: 2002. pmid:23788126
  32. 32. Peach WJ, Sheehan DK, Kirby WB. Supplementary feeding of mealworms enhances reproductive success in garden nesting House Sparrows Passer domesticus. Bird Study. 2014;61: 378–385.
  33. 33. Pravosudov VV, Grubb TC Jr. Energy management in passerine birds during the nonbreeding season: a review. In: Nolan V Jr, Ketterson ED, Thompson CF, editors. Current Ornithology. New York: Springer; 1997. pp. 189–234.
  34. 34. Cuthill IC, Maddocks SA, Weall CV, Jones EK. Body mass regulation in response to changes in feeding predictability and overnight energy expenditure. Behav Ecol. 2000;11: 189–195.
  35. 35. Witter MS, Cuthill IC. The ecological costs of avian fat storage. Philos Trans R Soc B Biol Sci. 1993;340: 73–92.
  36. 36. Swanson DL. Seasonal metabolic variation in birds: functional and mechanistic correlates. In: Thompson CF, editor. Current Ornithology. New York: Springer; 2010. pp. 75–129.
  37. 37. Brodin A. Theoretical models of adaptive energy management in small wintering birds. Philos Trans R Soc B Biol Sci. 2007;362: 1857–1871.
  38. 38. Sol D, Santos DM, Garcia J, Cuadrado M. Competition for food in urban pigeons: the cost of being juvenile. The Condor. 1998;100: 298–304.
  39. 39. Mennechez G, Clergeau P. Settlement of breeding European starlings in urban areas: importance of lawns vs. anthropogenic wastes. In: Marzluff JM, Bowman R, Donnelly R, editors. Avian Ecology and Conservation in an Urbanizing World. Norwell, Massachusetts: Kluwer Academic Publishers; 2001. pp. 275–287.
  40. 40. Prange S, Gehrt SD, Wiggers EP. Influences of anthropogenic resources on raccoon (Procyon lotor) movements and spatial distribution. J Mammal. 2004;85: 483–490.
  41. 41. Sauter A, Bowman R, Schoech SJ, Pasinelli G. Does optimal foraging theory explain why suburban Florida scrub-jays (Aphelocoma coerulescens) feed their young human-provided food? Behav Ecol Sociobiol. 2006;60: 465–474.
  42. 42. Green AJ. Mass/length residuals: measures of body condition or generators of spurious results? Ecology. 2001;82: 1473–1483.
  43. 43. Labocha MK, Hayes JP. Morphometric indices of body condition in birds: a review. J Ornithol. 2012;153: 1–22.
  44. 44. Kaiser A. A New Multi-Category Classification of Subcutaneous Fat Deposits of Songbirds (Una Nueva Clasificación, con Multi-categorías, para los Depósitos de Grasa en Aves Canoras). J Field Ornithol. 1993;64: 246–255.
  45. 45. Brown ME. Assessing body condition in birds. In: Nolan V Jr, Ketterson ED, editors. Current Ornithology. New York: Springer; 1996. pp. 67–135.
  46. 46. Leloutre C, Gouzerh A, Angelier F. Hard to fly the nest: A study of body condition and plumage quality in house sparrow fledglings. Curr Zool. 2014;60: 449–459.
  47. 47. Gosler AG. Environmental and social determinants of winter fat storage in the great tit Parus major. J Anim Ecol. 1996;65: 1–17.
  48. 48. Krams I, Cirule D, Suraka V, Krama T, Rantala MJ, Ramey G. Fattening strategies of wintering great tits support the optimal body mass hypothesis under conditions of extremely low ambient temperature. Funct Ecol. 2010;24: 172–177.
  49. 49. Cherel Y, Robin J-P, Heitz A, Calgari C, Le Maho Y. Relationships between lipid availability and protein utilization during prolonged fasting. J Comp Physiol B. 1992;162: 305–313. pmid:1506487
  50. 50. Jenni L, Jenni-Eiermann S. Fuel supply and metabolic constraints in migrating birds. J Avian Biol. 1998;29: 521–528.
  51. 51. Khalilieh A, McCue MD, Pinshow B. Physiological responses to food deprivation in the house sparrow, a species not adapted to prolonged fasting. Am J Physiol-Regul Integr Comp Physiol. 2012;303: R551–R561. pmid:22785424
  52. 52. Lindström J. Early development and fitness in birds and mammals. Trends Ecol Evol. 1999;14: 343–348. pmid:10441307
  53. 53. Bókony V, Seress G, Nagy S, Lendvai ÁZ, Liker A. Multiple indices of body condition reveal no negative effect of urbanization in adult house sparrows. Landsc Urban Plan. 2012;104: 75–84.
  54. 54. Giraudeau M, McGraw KJ. Physiological correlates of urbanization in a desert songbird. Integr Comp Biol. 2014;54: 622–632. pmid:24812330
  55. 55. Fair J, Whitaker S, Pearson B. Sources of variation in haematocrit in birds. Ibis. 2007;149: 535–552.
  56. 56. Williams TD, Challenger WO, Christians JK, Evanson M, Love O, Vezina F. What causes the decrease in haematocrit during egg production? Funct Ecol. 2004;18: 330–336.
  57. 57. Bowers EK, Hodges CJ, Forsman AM, Vogel LA, Masters BS, Johnson BG, et al. Neonatal body condition, immune responsiveness, and hematocrit predict longevity in a wild bird population. Ecology. 2014;95: 3027–3034. pmid:25505800
  58. 58. Hõrak P, Ots I, Murumägi A. Haematological health state indices of reproducing Great Tits: a response to brood size manipulation. Funct Ecol. 1998;12: 750–756.
  59. 59. McEwen BS, Wingfield JC. The concept of allostasis in biology and biomedicine. Horm Behav. 2003;43: 2–15. pmid:12614627
  60. 60. Landys MM, Ramenofsky M, Wingfield JC. Actions of glucocorticoids at a seasonal baseline as compared to stress-related levels in the regulation of periodic life processes. Gen Comp Endocrinol. 2006;148: 132–149. pmid:16624311
  61. 61. Cherel Y, Robin J-P, Walch O, Karmann H, Netchitailo P, Le Maho Y. Fasting in king penguin. I. Hormonal and metabolic changes during breeding. Am J Physiol-Regul Integr Comp Physiol. 1988;254: R170–R177.
  62. 62. Lynn SE, Breuner CW, Wingfield JC. Short-term fasting affects locomotor activity, corticosterone, and corticosterone binding globulin in a migratory songbird. Horm Behav. 2003;43: 150–157. pmid:12614645
  63. 63. Spée M, Beaulieu M, Dervaux A, Chastel O, Le Maho Y, Raclot T. Should I stay or should I go? Hormonal control of nest abandonment in a long-lived bird, the Adélie penguin. Horm Behav. 2010;58: 762–768. pmid:20691185
  64. 64. DuRant SE, Hopkins WA, Hepp GR, Romero LM. Energetic constraints and parental care: Is corticosterone indicative of energetic costs of incubation in a precocial bird? Horm Behav. 2013;63: 385–391. pmid:23232333
  65. 65. Angelier F, Wingfield JC, Parenteau C, Pellé M, Chastel O. Does short-term fasting lead to stressed-out parents? A study of incubation commitment and the hormonal stress responses and recoveries in snow petrels. Horm Behav. 2015;67: 28–37. pmid:25456104
  66. 66. Angelier F, Shaffer SA, Trouvé C, Chastel O. Corticosterone and foraging behavior in a pelagic seabird. Physiol Biochem Zool. 2007;80: 283–292. pmid:17390284
  67. 67. Angelier F, Giraudeau M, Chastel O. Are stress hormone levels a good proxy of foraging success? An experiment with king penguins, Aptenodytes patagonicus. J Exp Biol. 2009;212: 2824–2829. pmid:19684217
  68. 68. Romero LM, Wikelski M. Corticosterone levels predict survival probabilities of Galapagos marine iguanas during El Nino events. Proc Natl Acad Sci. 2001;98: 7366–7370. pmid:11416210
  69. 69. Kitaysky AS, Wingfield JC, Piatt JF. Dynamics of food availability, body condition and physiological stress response in breeding black-legged kittiwakes. Funct Ecol. 1999;13: 577–584.
  70. 70. Kitaysky AS, Kitaiskaia EV, Wingfield JC, Piatt JF. Dietary restriction causes chronic elevation of corticosterone and enhances stress response in red-legged kittiwake chicks. J Comp Physiol B. 2001;171: 701–709. pmid:11765979
  71. 71. Breuner CW, Patterson SH, Hahn TP. In search of relationships between the acute adrenocortical response and fitness. Gen Comp Endocrinol. 2008;157: 288–295. pmid:18602555
  72. 72. Bonier F, Martin PR, Moore IT, Wingfield JC. Do baseline glucocorticoids predict fitness? Trends Ecol Evol. 2009;24: 634–642. pmid:19679371
  73. 73. Goutte A, Angelier F, Welcker J, Moe B, Clément-Chastel C, Gabrielsen GW, et al. Long-term survival effect of corticosterone manipulation in black-legged kittiwakes. Gen Comp Endocrinol. 2010;167: 246–251. pmid:20338171
  74. 74. Walker BG, Boersma PD, Wingfield JC. Field endocrinology and conservation biology. Integr Comp Biol. 2005;45: 12–18. pmid:21676739
  75. 75. Ruiz G, Rosenmann M, Novoa FF, Sabat P. Hematological parameters and stress index in rufous-collared sparrows dwelling in urban environments. The Condor. 2002;104: 162–166.
  76. 76. Partecke J, J Van’t Hof T, Gwinner E. Underlying physiological control of reproduction in urban and forest-dwelling European blackbirds Turdus merula. J Avian Biol. 2005;36: 295–305.
  77. 77. Fokidis HB, Greiner EC, Deviche P. Interspecific variation in avian blood parasites and haematology associated with urbanization in a desert habitat. J Avian Biol. 2008;39: 300–310.
  78. 78. Liker A, Papp Z, Bókony V, Lendvai AZ. Lean birds in the city: body size and condition of house sparrows along the urbanization gradient. J Anim Ecol. 2008;77: 789–795. pmid:18479344
  79. 79. Bókony V, Kulcsár A, Liker A. Does urbanization select for weak competitors in house sparrows? Oikos. 2010;119: 437–444.
  80. 80. Chávez-Zichinelli CA, Macgregor-Fors I, Quesada J, Talamás Rohana P, Romano MC, Valdéz R, et al. How Stressed are Birds in an Urbanizing Landscape? Relationships Between the Physiology of Birds and Three Levels of Habitat Alteration: ?`Qué Tan Estresadas Están las Aves en un Paisaje Urbanizado? Relaciones Entre la Fisiología de las Aves y Tres Niveles de Alteración de Hábitat. The Condor. 2013;115: 84–92.
  81. 81. Bonier F, Martin PR, Sheldon KS, Jensen JP, Foltz SL, Wingfield JC. Sex-specific consequences of life in the city. Behav Ecol. 2007;18: 121–129.
  82. 82. Schoech SJ, Bowman R, Bridge ES, Boughton RK. Baseline and acute levels of corticosterone in Florida Scrub-Jays (Aphelocoma coerulescens): Effects of food supplementation, suburban habitat, and year. Gen Comp Endocrinol. 2007;154: 150–160. pmid:17624348
  83. 83. French SS, Fokidis HB, Moore MC. Variation in stress and innate immunity in the tree lizard (Urosaurus ornatus) across an urban–rural gradient. J Comp Physiol B. 2008;178: 997–1005. pmid:18594834
  84. 84. Fokidis HB, Orchinik M, Deviche P. Corticosterone and corticosteroid binding globulin in birds: relation to urbanization in a desert city. Gen Comp Endocrinol. 2009;160: 259–270. pmid:19116155
  85. 85. Zhang S, Lei F, Liu S, Li D, Chen C, Wang P. Variation in baseline corticosterone levels of Tree Sparrow (Passer montanus) populations along an urban gradient in Beijing, China. J Ornithol. 2011;152: 801–806.
  86. 86. Costantini D, Greives TJ, Hau M, Partecke J. Does urban life change blood oxidative status in birds? J Exp Biol. 2014;217: 2994–2997. pmid:24948638
  87. 87. Giraudeau M, Mousel M, Earl S, McGraw K. Parasites in the city: degree of urbanization predicts poxvirus and coccidian infections in house finches (Haemorhous mexicanus). PLoS One. 2014;9: e86747. pmid:24503816
  88. 88. Grunst ML, Rotenberry JT, Grunst AS. Variation in adrenocortical stress physiology and condition metrics within a heterogeneous urban environment in the song sparrow Melospiza melodia. J Avian Biol. 2014;45: 574–583.
  89. 89. Herrera-Dueñas A, Pineda J, Antonio MT, Aguirre JI. Oxidative stress of House Sparrow as bioindicator of urban pollution. Ecol Indic. 2014;42: 6–9.
  90. 90. Foltz SL, Davis JE, Battle KE, Greene VW, Laing BT, Rock RP, et al. Across time and space: Effects of urbanization on corticosterone and body condition vary over multiple years in song sparrows (Melospiza melodia). J Exp Zool Part Ecol Genet Physiol. 2015;323: 109–120.
  91. 91. De Laet J, Summers-Smith JD. The status of the urban house sparrow Passer domesticus in north-western Europe: a review. J Ornithol. 2007;148: 275–278.
  92. 92. Shaw LM, Chamberlain D, Evans M. The House Sparrow Passer domesticus in urban areas: reviewing a possible link between post-decline distribution and human socioeconomic status. J Ornithol. 2008;149: 293–299.
  93. 93. Seress G, Bókony V, Pipoly I, Szép T, Nagy K, Liker A. Urbanization, nestling growth and reproductive success in a moderately declining house sparrow population. J Avian Biol. 2012;43: 403–414.
  94. 94. Chavez-Zichinelli CA, MacGregor-Fors I, Talamas Rohana P, Valdez R, Romano MC, Schondube JE. Stress responses of the House Sparrow (Passer domesticus) to different urban land uses. Landsc Urban Plan. 2010;98: 183–189.
  95. 95. Angelier F, Tonra CM, Holberton RL, Marra PP. How to capture wild passerine species to study baseline corticosterone levels. J Ornithol. 2010;151: 415–422.
  96. 96. Anderson TR. Biology of the ubiquitous house sparrow, From Genes to Populations. Oxford: Oxford University Press; 2006.
  97. 97. Romero LM, Reed JM. Collecting baseline corticosterone samples in the field: is under 3 min good enough? Comp Biochem Physiol A Mol Integr Physiol. 2005;140: 73–79. pmid:15664315
  98. 98. Wingfield JC, Davey KG, Peter RE, Tobe SS. Modulation of the adrenocortical response to stress in birds. Perspectives in Comparative Endocrinology. Canada, Ottawa: National Research Council; 1994. pp. 520–528.
  99. 99. Peig J, Green AJ. New perspectives for estimating body condition from mass/length data: the scaled mass index as an alternative method. Oikos. 2009;118: 1883–1891.
  100. 100. Peig J, Green AJ. The paradigm of body condition: a critical reappraisal of current methods based on mass and length. Funct Ecol. 2010;24: 1323–1332.
  101. 101. Fridolfsson A-K, Ellegren H. A simple and universal method for molecular sexing of non-ratite birds. J Avian Biol. 1999;30: 116–121.
  102. 102. Lormée H, Jouventin P, Trouve C, Chastel O. Sex-specific patterns in baseline corticosterone and body condition changes in breeding Red-footed Boobies Sula sula. Ibis. 2003;145: 212–219.
  103. 103. R Core Team. R: A Language and Environment for Statistical Computing [Internet]. R Foundation for Statistical Computing; 2014. Available:
  104. 104. Graham MH. Confronting multicollinearity in ecological multiple regression. Ecology. 2003;84: 2809–2815.
  105. 105. Pap PL, Vágási CI, Czirják GÁ, Barta Z. Diet quality affects postnuptial molting and feather quality of the house sparrow (Passer domesticus): interaction with humoral immune function? Can J Zool. 2008;86: 834–842.
  106. 106. De Coster G, De Laet J, Vangestel C, Adriaensen F, Lens L. Citizen science in action—Evidence for long-term, region-wide House Sparrow declines in Flanders, Belgium. Landsc Urban Plan. 2015;134: 139–146.
  107. 107. Richner H. Habitat-specific growth and fitness in carrion crows (Corvus corone corone). J Anim Ecol. 1989;58: 427–440.
  108. 108. Evans KL, Gaston KJ, Sharp SP, McGowan A, Hatchwell BJ. The effect of urbanisation on avian morphology and latitudinal gradients in body size. Oikos. 2009;118: 251–259.
  109. 109. Peach WJ, Vincent KE, Fowler JA, Grice PV. Reproductive success of house sparrows along an urban gradient. Anim Conserv. 2008;11: 493–503.
  110. 110. Eeva T, Lehikoinen E. Growth and mortality of nestling great tits (Parus major) and pied flycatchers (Ficedula hypoleuca) in a heavy metal pollution gradient. Oecologia. 1996;108: 631–639.
  111. 111. Meillère A, Brischoux F, Angelier F. Impact of chronic noise exposure on antipredator behavior: an experiment in breeding house sparrows. Behav Ecol. 2015;26: 569–577.
  112. 112. MacLeod R, Barnett P, Clark J, Cresswell W. Mass-dependent predation risk as a mechanism for house sparrow declines? Biol Lett. 2006;2: 43–46. pmid:17148322
  113. 113. Bergman C. Über die Verhältnisse der Wärmeökonomie der Thiere zu ihrer Grösse. Gött Stud. 1847;3: 595–708.
  114. 114. Seebohm H. Birds of Siberia. London: Murray; 1901.
  115. 115. McIntyre NE. Ecology of urban arthropods: a review and a call to action. Ann Entomol Soc Am. 2000;93: 825–835.
  116. 116. Heiss RS, Clark AB, McGowan KJ. Growth and nutritional state of American crow nestlings vary between urban and rural habitats. Ecol Appl. 2009;19: 829–839. pmid:19544727
  117. 117. Gibb H, Hochuli DF. Habitat fragmentation in an urban environment: large and small fragments support different arthropod assemblages. Biol Conserv. 2002;106: 91–100.
  118. 118. Monaghan P. Early growth conditions, phenotypic development and environmental change. Philos Trans R Soc B Biol Sci. 2008;363: 1635–1645.
  119. 119. Brotons L, Broggi J. Influence of morphology on winter residence and recruitment in juvenile coal tits (Parus ater) after the post-fledging period. Ecoscience. 2003;10: 273–282.
  120. 120. Gebhardt-Henrich S, Richner H. Causes of growth variation and its consequences for fitness. Oxf Ornithol Ser. 1998;8: 324–339.
  121. 121. Gardner JL, Peters A, Kearney MR, Joseph L, Heinsohn R. Declining body size: a third universal response to warming? Trends Ecol Evol. 2011;26: 285–291. pmid:21470708
  122. 122. Heidinger BJ, Nisbet IC, Ketterson ED. Older parents are less responsive to a stressor in a long-lived seabird: a mechanism for increased reproductive performance with age? Proc R Soc Lond B. 2006;273: 2227–2231.
  123. 123. Lendvai ÁZ, Giraudeau M, Chastel O. Reproduction and modulation of the stress response: an experimental test in the house sparrow. Proc R Soc B. 2007;274: 391–397. pmid:17164203
  124. 124. Angelier F, Wingfield JC, Weimerskirch H, Chastel O. Hormonal correlates of individual quality in a long-lived bird: a test of the “corticosterone–fitness hypothesis.” Biol Lett. 2010;6: 846–849. pmid:20573614
  125. 125. Romero LM, Reed JM, Wingfield JC. Effects of weather on corticosterone responses in wild free-living passerine birds. Gen Comp Endocrinol. 2000;118: 113–122. pmid:10753573
  126. 126. Crino OL, Johnson EE, Blickley JL, Patricelli GL, Breuner CW. Effects of experimentally elevated traffic noise on nestling white-crowned sparrow stress physiology, immune function and life history. J Exp Biol. 2013;216: 2055–2062. pmid:23430998
  127. 127. Tartu S, Angelier F, Herzke D, Moe B, Bech C, Gabrielsen GW, et al. The stress of being contaminated? Adrenocortical function and reproduction in relation to persistent organic pollutants in female black legged kittiwakes. Sci Total Environ. 2014;476–477: 553–560. pmid:24496028
  128. 128. Vitousek MN, Jenkins BR, Safran RJ. Stress and success: Individual differences in the glucocorticoid stress response predict behavior and reproductive success under high predation risk. Horm Behav. 2014;66: 812–819. pmid:25461975
  129. 129. Dantzer B, Fletcher QE, Boonstra R, Sheriff MJ. Measures of physiological stress: a transparent or opaque window into the status, management and conservation of species? Conserv Physiol. 2014;2: cou023.
  130. 130. Evans KL, Gaston KJ, Sharp SP, McGowan A, Simeoni M, Hatchwell BJ. Effects of urbanisation on disease prevalence and age structure in blackbird Turdus merula populations. Oikos. 2009;118: 774–782.