http://orcid.org/0000-0003-3253-2362
Figures
Abstract
Animals in urban environments face challenging situations and have to cope with human activities. This study investigated the ecology and behaviour of a population of European hamsters (Cricetus cricetus) living in the city centre of Vienna (Austria). We recorded the surface activities of 35 hamsters in May 2015. Each focal animal was observed for 15 minutes, and a total of 66 focal samples were analysable. As a prey species in an environment teeming with human activities, we predicted a high level of vigilance by the hamsters. The results show that while animals dedicated a lot of time to vigilance, most of their time was spent foraging. The study also explores whether the frequency of vigilance behaviours differ between males and females. We found that vigilance behaviours were expressed in a different manner by males and females. Finally, we investigated the distribution of the burrows on green spaces depending on proximity to trees and on noise levels. We found a biased distribution of burrows, with a spatial preference for location protected by the vegetation and distant to noise sources. Although burrows were located preferentially under vegetation cover, levels of noise did not determine their positions. Moreover, this species does not respond to disturbances like daily urban noises, probably due to habituation. The common hamster is an endangered species; our results lead to a greater knowledge of its behaviour in a persistent urban population.
Citation: Flamand A, Rebout N, Bordes C, Guinnefollau L, Bergès M, Ajak F, et al. (2019) Hamsters in the city: A study on the behaviour of a population of common hamsters (Cricetus cricetus) in urban environment. PLoS ONE 14(11): e0225347. https://doi.org/10.1371/journal.pone.0225347
Editor: Christopher M. Somers, University of Regina, CANADA
Received: July 3, 2019; Accepted: November 1, 2019; Published: November 21, 2019
Copyright: © 2019 Flamand et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: This work was supported by the LIFE + Biodiversity grant No. LIFE12 BIO/FR/000979 and the Ministère de l’Ecologie, du Développement durable et de l’Energie. CW and OP received this award. URL: https://ec.europa.eu/easme/en/life; https://www.ecologique-solidaire.gouv.fr/. The funders played no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Urbanization is a growing phenomenon that has deep implications for ecosystems. One of them is the destruction of wildlife habitat, mainly in forest or agricultural areas [1,2]. When its habitat is destroyed, there are two possible solutions for an animal: moving to a more suitable environment or trying to face the new one [3]. In this latter situation, individuals have to adjust to urban conditions via a process called synantropism [4]. An often mentioned key element of successful adaptation in synantropic species is behavioural plasticity [5,6]. It could induce modifications like change in diet [5], adjustment of activity patterns according to human activities [7–9] or decreased levels of fear towards humans [10].
The common hamster (Cricetus cricetus) is one such synantropic species [11] that can be found on the outskirts or even in the centre of several large European cities [12,13]. It demonstrates some flexibility specific to urban context, which have been described above [14,15]. Nonetheless, this species–native to environments such as the steppes and grasslands–is usually found in agricultural areas of Europe and Asia [16]. The destruction of its natural habitat mainly caused by changes in agricultural practices and urban spread could explain its presence in towns [11,17]. Actually, some urban populations were already settled in these areas before the city expanded and they have adapted to their new environment.
The common hamster is a hibernating rodent, active from March to September [18]. Its active period is dedicated to reproduction and the storage of food in its burrow, in anticipation of hibernation. Over the previous decades and throughout the western part of the distribution area of the species, the populations of hamsters have dramatically declined [17]. Hence, the species is strictly protected by the Appendix IV of the Fauna-Flora-Habitat Directive in all countries of the European Union included in its distribution range (Austria, Belgium, Bulgaria, Czech Republic, Germany, France, Netherlands, Poland, Romania, Slovakia, and Slovenia) [19]. Several of these countries took some conservation measures including reintroduction programs, reinforcement of the national legislation and agricultural measures [17]. The species is recognized as an umbrella species which means that these protection measures would also provide benefits to other species and more broadly to biodiversity [20]. Despite extensive actions, the decline of rural populations is hard to counteract. The accommodation of the species to urban areas could be regarded as a chance to prevent the extinction process. It is thus of prime interest to study populations that have succeeded to adapt to an urban environment [21]. Some urban populations have been monitored for several years, providing information about settlement and distribution of populations as well as about reproduction and hibernation [11,16,22]. Nevertheless, knowledge is still missing on behaviour, an aspect addressed by few studies but not in depth [23,24]. Studies on behaviour–a crucial feature of adaptation–would provide a new and broader perspective on the species in urban areas. By gathering information on a free-ranging population living in urban areas, the ultimate objective of this study is to introduce hamsters into similar environments for conservation purposes as experienced in the Alister program (Life + Biodiversity, LIFE12-BIO-FR-000979) [25]. Characterizing beneficial and disruptive elements of the environment could help providing a suitable environment contributing to establish these urban populations.
For such purpose, the current study investigates the behaviour of an urban population of hamsters, and specifically considers how they allocate their time above ground. We focused on their activity budget (time spent for each activity at each trip). We assumed that they would be particularly vigilant and thus spend relatively short periods of time foraging given the inherent anthropic pressures of the urban environment. The range of vigilance behaviours expressed in response to this environment was also examined. Given the different reproductive strategies of males and female, males search for the burrows of females for mating purpose, while females need to forage given the high energetic demands of reproduction, the differences between males and females were analysed for both activity budget and vigilance behaviours. Additionally, the use of green spaces was also studied through the location of burrows depending on proximity to trees and on noise levels. As hamsters are prey animals, we expected a heterogeneous distribution with a spatial preference for location protected by vegetation and far from noise sources possibly perceived as a threat, preventing them to hear an approaching predator or to communicate.
Material and methods
Study site
The study area was located on the grounds of the Kaiser-Franz-Josef hospital in the South of the city of Vienna, Austria (geographic coordinates: 48°10'27.9"N 16°21'02.8"E, cf. Fig 1A and Fig 1B). This site is of interest because it has some classic characteristics of the urban environment (i.e. human presence and activities, lighting, traffic, etc.) and is not close to crops in which the species usually inhabits. This allows us to study how the common hamster deals with these urban elements without the presence of crops that provide food and protective vegetation cover. The results obtained in this study could constitute indications for allowing the implantation of hamsters in comparable sites for conservation purposes.
Location of the study site in Europe (A) and in Vienna (B). (A) Location of the country of study (B) Location of the study site in the city of Vienna.
The study site covers 4.32 ha, including 2.85 ha of green areas (total surface) surrounding the hospital. These green spaces are mainly composed of grass with trees and bushes also bordering the plots. The hamsters were settled heterogeneously on these plots. The studied population of free-ranging hamsters was already present before the hospital was built in 1884. Since 2013, the University of Vienna monitored this population [22] which seems to cope with urban conditions, especially through its successful reproduction and usual hibernation pattern [26,27]. Despite slight fluctuations over the years, this population of about 170 individuals is considered stable.
Procedure
Data were collected between 30 April and 26 May 2015, during the breeding season of the common hamster. We first estimated the number of burrows that were active i.e. inhabited by an individual, indicated by the presence of faeces, recent feeding food and/or recent excavated soil and inactive i.e. no longer used, indicated by the vegetation at the entrance and the absence of pathways around it. As it was impossible to ascertain which entrances were linked to a burrow system, every single entrance was defined as a burrow [28]. At the outset of the study, 685 burrows (194 active, 491 inactive) were detected. This number grew to 787 at the end of the study (208 active, 579 inactive). The spatial positions of these burrows were also recorded to evaluate whether their location was linked to the vicinity of trees or bushes and to the noise disturbances.
To characterize the hamster habitat, 25 random points–hereafter referred to as plots–were randomly selected on the lawns. The plots were 25 metres apart, and each had a radius of 12 meters (cf. Fig 2). For each plot, the level of ambient noise was assessed with a sonometer (Testo, reference 815). The recorded noises were typical of urban environment (motorised vehicles, construction activities, pedestrians, etc.) [29]. Noise intensity was recorded daily at the beginning of each observation session, in the morning and in the evening.
Regarding proximity to a vegetation cover, a burrow was considered close if located at less than one metre from a tree or bush.
Secondly, the behaviour of 35 individuals (13 adult males, 18 adult females and 4 of unidentified sex) was monitored. Individuals were identified by fur-marking (see [30] for a detailed description of the method used). Observation sessions were performed from the same plots as those used for the characterisation of the habitat. The plot of each session randomly changed on a daily basis. Two observers in different locations recorded the behaviour of hamsters above ground with a video camera (Sony Handycam HDR-CX190E), observing from a distance of 6 to 20 meters to the animal. Each individual was observed using the focal sampling method [31] for a 15-minute period (the collected sequences are then referred as focal periods). If the focal individual disappeared from view, the observer stopped filming until it reappeared. As one animal could have been observed several times, the number of focal periods per animal has been nested by individual in the statistical analyses.
After five days of preliminary observations throughout the day and night, observation sessions alternated between 6 a.m. to 9 a.m. (morning session) one day, and 5 p.m. to 9 p.m. (evening session) the next day. These two periods correspond to the activity peaks reported in urban environments for this species [32]. Indeed, the common hamster is often described as a nocturnal species in the literature [33], yet it is also active at dusk [32] and even during the daytime [34]. Our observations, carried out at two different moments (morning and evening), allowed us to compare the repartition of activities (i.e. activity budget) and the frequency of vigilance behaviours according to the period during which the animals are active.
The observational protocols followed EU Directive 2010/63/EU guidelines for animal experiments. As this study does not include manipulations or direct interactions with the individuals studied, no specific permissions were required. However, the director of the hospital gave us authorization to observe the hamsters.
Behavioural data collection
Overall, 66 focal periods (over a total of 156 hours of field work) were collected. After sex identification and the exclusion of poor-quality images, 54 focal periods remained. Video footage analysis was carried out according to the ethogram developed by Ziomek et al. (2009) [23], which was completed with our observations (cf. Table 1 for description of behaviours). During the observations, all behaviours were precisely recorded and for rare ones, regrouped in the category “other” (cf. Table 1) in the following statistical analysis.
Statistical analysis
We performed statistical analyses using R 3.5.2 [35] and significance was set at p < 0.05.
We first explored the distribution of burrows according to the proximity to trees and bushes in order to know if this parameter had an influence on the location of the burrows. A chi-squared test was used to compare the number of burrows found in the centre of the lawns (without any cover protection) with the number of burrows located near trees. We subsequently investigated whether the number of burrows on each plot was dependent on noise intensity. To this end, we ran a generalized linear model (GLM) analysis in which the response variable was the number of burrows and the explicative variable was the noise intensity. Because the number of burrows was a count variable, we therefore used a Poisson distribution. The dredge function of the “MuMIn” package was used to select the best-fitting models, based on corrected Akaike Information Criterion (AICc), delta AIC (ΔAIC) and the Akaike weight [36] (S1 Table).
Analyses on activity budget of individuals were then conducted: at each surface trip of a hamster, the time spent for each activity was measured, giving a ratio of the different activities per trip. These different activity ratios were then compared according to sex (male or female) and time of day (morning or evening). These analyses were performed on 31 adult individuals among 35, since it was impossible to determine the sex of four focal individuals from the data and videos. We ran generalized linear mixed model (GLMM) analyses using the “lme4” package [37]. These were GLMMs of proportion in which success was considered to be the time spent on one activity and failure was the time spent on other activities. We therefore used a binomial distribution and a logit link function. The target variable was the proportion of time attributed to a given activity during the active period, and fixed factors were: type of activity (foraging, vigilance, social interactions, locomotion, burrow and other), sex and time of day. The target variable was expressed as proportions to allow for differences in video durations. In order to take into account the repeatability of individuals according to the observation sessions, individuals were considered as random factors and observation sessions were nested in individuals. After selecting suitable predictors (detailed above as fixed factors), we checked for the absence of correlation between these predictors using variance inflation factor (VIF). In each model, all VIF values were lower than 3. The dredge function of the “MuMIn” package was also used for model selection. We chose the model with the lowest AICc [38] which led us to exclude the time of day of the analysis (S2 Table). Post-hoc tests were performed with the “emmeans” package [39] to investigate the results of interactions between qualitative variables.
The same procedure was followed for vigilance behaviours analyses: at each surface trip of a hamster, the frequency of specific vigilance behaviours was measured, giving a ratio of specific vigilance behaviours on the total vigilance behaviours expressed during a surface trip. We compared the ratios of these different vigilance behaviours between type of vigilance behaviour (e.g. short-term freezing, long-term freezing, head-rearing or monitoring) and sex, and between type of vigilance and time of day. Our objective was to explore if the different type of vigilance behaviour differed according to sex or time of day. A GLMM analysis was performed, using the same approach as described above for the activity budget but with the frequency proportion of each vigilance as target variable, and type of activity, sex and time of day as fixed factors. The model selected led us to exclude the time of day of the analysis (S3 Table).
Results
Location of burrows
The influence of the proximity of trees and bushes and of noise level on the location of the burrow has been analysed. Burrows were not equally distributed (chi-squared test: 6.98, df = 1, p<0.01). They were more often located near trees and bushes (n = 429, i.e. 55% of the burrows) rather than in the middle of the lawns (n = 355, i.e. 45% of the burrows). Moreover, noise intensity had no effect on the distribution of burrows across the different plots (estimate ± SD: -0.060 ± 0.045, z = -1.32, p = 0.186).
Activity budget
Activity time ratios were compared between activity and sex (N = 31, n = 53 with N the number of focal animals and n the number of sessions used for comparison). The best-fitting model included activity, sex and the interaction between activity and sex (S2 Table: model 1). Post-hoc comparisons of the interaction between activity and sex revealed that females spent more time foraging than displaying vigilance behaviours (0.588 ± 0.031 vs 0.116 ± 0.02, z = 10.24, p <0.001). The proportion of time spent foraging was also higher than the time spent in social interactions (0.588 ± 0.031 vs 0.0032 ± 0.004, z = 5.45, p <0.001), in locomotion (0.588 ± 0.031 vs 0.036 ± 0.012, z = 10.13, p <0.001), in burrow (0.588 ± 0.031 vs 0.232 ± 0.026, z = 7.97, p <0.001) and in the “other” category (0.588 ± 0.031 vs 0.004 ± 0.003, z = 5.79, p <0.001). The proportion of time dedicated to vigilance behaviours was higher than that observed for social interactions (0.116± 0.02 vs 0.0032 ± 0.004, z = -3.29, p = 0.013), locomotion (0.116 ± 0.02 vs 0.036 ± 0.012, z = -3.25, p = 0.015) and in the “other” category (0.116 ± 0.02 vs. 0.004 ± 0.003, z = -3.42, p = 0.008). The proportion of time spent in the burrow was higher than in vigilance (0.232 ± 0.026 vs 0.116 ± 0.02, z = 3.39, p = 0.009), in locomotion (0.232 ± 0.026 vs 0.036 ± 0.012, z = -5.7, p <0.001), in social interactions (0.232 ± 0.026 vs 0.0032 ± 0.004, z = -4.06, p<0.001), and in the “other” category (0.232 ± 0.026 vs 0.004 ± 0.003, z = -4.26, p<0.001). No other comparisons yielded any significant difference.
Males spent significantly more time foraging than interacting socially (0.299 ± 0.043 vs 0.018 ± 0.013, z = 4.33, p <0.001) or in locomotion (0.299 ± 0.043 vs 0.044 ± 0.019, z = 4.48, p <0.001). More time was dedicated to vigilance than to social interactions (0.234 ± 0.04 vs 0.018 ± 0.013, z = -3.82, p = 0.002), locomotion (0.234 ± 0.04 vs 0.044 ± 0.019, z = -3.73, p = 0.003) and in the “other” category (0.234 ± 0.04 vs 0.032 ± 0.016, z = -3.86, p = 0.002). More time was spent in the burrow than in locomotion (0.274 ± 0.042 vs 0.044 ± 0.019, z = -4.22, p <0.001), in social interactions (0.274 ± 0.042 vs 0.018 ± 0.013, z = -4.15, p <0.001) and in the “other” category (0.274 ± 0.042 vs 0.032 ± 0.016, z = -4.28, p<0.001). We did not find any other significant contrast.
The comparison of male and female activity budgets (Fig 3) revealed that females spent significantly more time foraging than males (0.588 ± 0.031 vs 0.299 ± 0.043, z = 5.042; p <0.001) and that males spent more time displaying vigilance behaviours than females (0.232 ± 0.040 vs 0.116 ± 0.020, z = -2.82; p = 0.005). No statistically significant difference was found for other activities (female vs male: locomotion: 0.036 ± 0.012 vs 0.044 ± 0.019, z = -0.38; p = 0.71, social interactions: 0.0032 ± 0.004 vs 0.018 ± 0.013, z = -1.36; p = 0.18, burrow: 0.232 ± 0.026 vs 0.274 ± 0.042 z = -0.87; p = 0.38, others: 0.004 ± 0.003 vs 0.032 ± 0.016 z = -1.89; p = 0.059).
Proportion of time dedicated to the different behavioural activities (represented by the boxes), f: female; m: male. Estimate ± SD. **: p<0.01, ***: p<0.001. Outliers are symbolized by dots.
Vigilance behaviours
Ratios of frequency of vigilance behaviours were compared between type of vigilance behaviour and sex (N = 30, n = 50 with N the number of focal animals and n the number of sessions used for comparison). The best-fitting model was explained by activity, sex and the interaction between activity and sex (S2 Table: model 1). Post-hoc analysis showed that females expressed a higher proportion of short-term freezing than head-rearing (0.41 ± 0.016 vs 0.31 ± 0.015, z = -4.86, p< 0.001). The proportion of short-term freezing was also higher than long-term freezing (0.41 ± 0.016 vs 0.24 ± 0.014 z = -7.96, p <0.001) and monitoring (0.41 ± 0.016 vs 0.037 ± 0.006, z = -15.97, p<0.001). Head-rearing was also more frequent than long-term freezing (0.31 ± 0.015 vs 0.24 ± 0.014, z = 3.20, p = 0.0075) and monitoring (0.31 ± 0.015 vs 0.037 ± 0.006, z = 13.31, p <0.001). The proportion of long-term freezing was higher than monitoring (0.24 ± 0.014 vs 0.037 ± 0.006, z = 11.40, p <0.001).
In males, the proportion of head-rearing was higher than long-term freezing (0.49 ± 0.020 vs 0.22 ± 0.017, z = 9.41, p <0.001), short-term freezing (0.49 ± 0.022 vs 0.22 ± 0.017, z = 8.72, p <0.001) and monitoring (0.49 ± 0.022 vs 0.065 ± 0.010, z = 9.53, p <0.001). Long-term freezing and short-term freezing were equally expressed (0.22 ± 0.017 vs 0.22 ± 0.017, z = 0.14, p = 0.99), but long-term freezing was more frequently expressed than monitoring (0.22 ± 0.017 vs 0.065 ± 0.010, z = 7.38, p <0.001). Short-term freezing was also more frequently expressed than monitoring (0.22 ± 0.017 vs 0.065 ± 0.010, z = -7.27, p <0.0001).
Comparison between sexes showed that females expressed more short-term freezing than males (0.41 ± 0.016 vs 0.22 ± 0.017, z = 7.71, p <0.001) and conversely, males expressed more head-rearing (0.49 ± 0.020 vs 0.31 ± 0.015, z = -7.20, p <0.001) and monitoring (0.065 ± 0.010 vs 0.037 ± 0.006, z = -2.50, p = 0.0124) than females (Fig 4). No intersex differences were found for long-term freezing (female vs male: 0.24 ± 0.014 vs 0.22 ± 0.017, z = 0.82, p = 0.41).
Proportion of frequency of vigilance behaviours (represented by the boxes), f: female; m: male. Estimate ± SD. *: p<0.05, ***: p<0.001. Outliers are reprezented by dots.
Discussion
Active period in urban areas
Location of burrows.
Burrows were more frequently located near trees and bushes than in open ground. This distribution has already been described several times in urban areas [13,40], and the highest burrow density in towns has been observed close to bushes [11]. Such location choices can be explained by the protection the vegetation provides against predators, and the availability of food near trees and bushes. Indeed, leaves, seeds and fruits make up a significant proportion of the urban hamster diet [41], and are almost unlimited thanks to the maintenance of plants by gardeners [40]. Moreover, the roots could also offer useful support for digging burrows and lead to more stable burrows. Interestingly, the benefits provided by this location seem to overcome the disadvantages of the proximity or level of noise disturbances, suggesting that hamsters dig their burrows regardless of this pressure. A large number of the disturbances recorded were urban ambient noises. In different bird species, urban noises are problematic because of the value of the acoustic channel in social communication [42]. In contrast to birds, hamsters do not seem to be sensitive to this particular urban feature [40]. The common hamster is a solitary species for which social interactions are rare [23]. The limited use of vocal communication in hamsters could explain their tolerance of, and/or indifference to, ambient noises [11,40,43]. This result is consistent with reports of burrows located along main streets that are high-traffic roads in Simferopol, Ukraine [11,16]. Moreover, the studied population has lived near this hospital for many generations and is probably accustomed to these repetitive disturbances [44], which are similar to a background noise, whatever their intensity. Francis and Barber (2013) [45] suggested the possibility of a long-term decrease in sensory capacities in urban species, which could also explain why this stable urban population no longer reacts to urban noises. To sum up, the vegetal criteria—providing food source, protection and favourable soil features- seems to have an importance in location of burrows in urban environment, contrarily to noise levels. In the interest of the species, this information could be useful for the management of the green spaces: adding as many fruit trees and bushes as possible in places where hamsters are settled could help ensure the success of their reintroduction in urban areas [46].
Foraging.
Our results show that foraging is the main activity in both male and female during their daily activity peaks, and this finding is in accordance with the species’ activity budget. Further, Hędrzak [24] demonstrate that suburban hamsters increase the return rate to their burrow and Ziomek et al. (2009) [23] found that hamsters tend to feed more inside their burrow than at the surface. This is in accordance with our results, which reveal that hamsters spend a large proportion of time inside their burrow during their activity period. This could also be explained by the proximity of certain food sources in the urban environment, allowing hamsters to consume their food directly inside their burrows. Thus, hamsters may forage and feed in a fractioned manner, with frequent round trips to their burrow. Such adjustment might allow hamsters to decrease the time exposed to threats outside their burrows and consume the food in a safety place.
Vigilance.
While foraging is the main activity of hamsters, we found that they also dedicate an important part of their time to vigilance. As a consequence, their daily foraging is often interrupted by these behaviours, which might engender energetic costs. For prey species, vigilance is a costly but fundamental antipredator behaviour that affects survival. Although the urban environment decreases the diversity of the common hamster’s natural predator species [11,16], mortality due to predation still exists [46]. The occurrence of vigilance could be due to predation risk, but it could also reflect a reaction to anthropogenic disturbances [5]. Indeed, hamsters that live in an urban environment are considered more cautious and vigilant than their rural counterparts [24,40].
Trade-off foraging-vigilance: Two different sex strategies.
Like many prey species, hamsters have to balance between foraging and vigilance [47] leading to different strategies in males and females during the breeding season. Indeed, we found that females spent more time foraging than males, a result that Feoktistova et al. (2014) [16] also found in hamsters later in the breeding season. This result is not surprising because females have high energy needs during the breeding period due to the reproduction costs of gestation and lactation [48]. The high availability of food in urban areas causes an early start of the breeding season [46] and lengthens its duration [7], entailing a particularly extended effort for females [26]. In addition, males change burrows frequently during the mating period when searching for females, and therefore probably store less food in their temporary burrow, leading to less foraging.
On the other hand, males dedicate more time to vigilance than females do. Sexual competition may lead males to increase their vigilance in order to detect the presence of potential competitors and/or avoid aggressive encounters [49].
Moreover, the different vigilance behaviours have variable energetic costs, and this could influence their relative expression in males and females. Among vigilance behaviours, males regularly express head-rearing and do so more often than females. This behaviour provides information about the environment and causes a short interruption of activities. It could even be expressed during foraging/feeding [50] reducing the cost of vigilance to some extent.
Females expressed more short-term freezing than males. Conversely to head-rearing, freezing (short or long) is an exclusive behaviour that implies a longer and complete interruption of the animal’s current activity. The hamster obtains limited information about the environment with this kind of behaviour, but its stillness has the advantage of not requiring any physical effort. Indeed, females focus their efforts on gestation and maternal care during the breeding season, so all other energetic costs due to spatial displacements could be restricted. Females may therefore choose a vigilance strategy that requires the least possible energetic effort. In contrast to males, their stationary behaviour could explain that they invest less time in vigilance behaviours.
Conclusion
In this urban population, hamsters select the location of their burrow in order to gain maximum benefits from their habitat. Moreover, the trade-off between foraging and vigilance differs depending on sex, potentially due to reproductive strategies. Although the common hamster does not seem to be influenced by the noise disturbances when selecting the location of its burrow, like other wildlife species are, it faces new stressors in urban conditions (i.e. human proximity, road traffic, light or soil pollution, etc.). The consequences of the resulting biological constraints [7] should be carefully monitored to ensure the conservation of this endangered species in urban settings for already existing populations. Additionally, the destruction of the natural habitat of the common hamster is constantly expanding everywhere in Western Europe, which has severe consequences on its conservation status. The results of the current study might be applied to arrange urban areas in order to render them suitable for reintroduction purposes of the species.
Supporting information
S1 Table. GLMM models selection table for the analysis of location of burrow according to noise intensity.
Models ranked by the Akaike Information Criterion (AICc): AICc computations and relative variable importance (weight) are indicated for each model. The best model is represented in bold.
https://doi.org/10.1371/journal.pone.0225347.s001
(DOCX)
S2 Table. GLMM models selection table for the analysis of the activity budget.
Models ranked by the Akaike Information Criterion (AICc): presence (+) for qualitative effects, AICc computations and relative variable importance (weight) are indicated for each model. The best model is represented in bold.
https://doi.org/10.1371/journal.pone.0225347.s002
(DOCX)
S3 Table. GLMM models selection table for the analysis of the vigilance behaviours.
Models ranked by the Akaike Information Criterion (AICc): presence (+) for qualitative effects, and AICc computations and relative variable importance (weight) are indicated for each model. The best model is represented in bold.
https://doi.org/10.1371/journal.pone.0225347.s003
(DOCX)
S1 File. Data file for the analysis of number of burrows according to noise intensity.
1st raw: Letter corresponding to the plot in the green areas where burrows are located, 2nd raw: number of active burrows found in each specific plot, 3rd raw: Mean of the noise intensity per plot (in dB).
https://doi.org/10.1371/journal.pone.0225347.s004
(CSV)
S2 File. Proportion of time dedicated to the different behavioural activities in females and males.
1st raw: Name of the observation session, 2nd raw: Time of the day (Morning or Evening), 3rd raw: Letter corresponding to the focal individual followed, 4th raw: Sex of the focal individual (female (f) or male (m)), 5th raw: Name of the activity performed by the focal individual (foraging, burrow, locomotion, others, social or vigilance), 6th raw: Duration of the activity of the focal individual, 7th raw: Total duration of the observed trip of the focal individual.
https://doi.org/10.1371/journal.pone.0225347.s005
(CSV)
S3 File. Frequency of vigilance behaviours in females and males.
1st raw: Name of the observation session, 2nd raw: Time of the day (Morning or Evening), 3rd raw: Letter corresponding to the focal individual followed, 4th raw: Sex of the focal individual (female (f) or male (m)), 5th raw: Name of the specific vigilance behaviour expressed by the focal individual (Head-rearing, monitoring, long-freezing or short-freezing), 6th raw: Frequency of the specific vigilance behaviour of the focal individual, 7th raw: Total frequency of the vigilance behaviours for a focal individual.
https://doi.org/10.1371/journal.pone.0225347.s006
(CSV)
Acknowledgments
We are grateful to the director of the Kaiser-Franz-Josef hospital for permitting access to the site during the field session. English language content has been edited by two professional copy editors (J. Munro and M. Guilhem).
References
- 1. McKinney M. Urbanization as a major cause of biotic homogenization. Biology Conservation. 2006; 127(3): 247–260.
- 2. Marzluff J, Ewing K. Restoration of fragmented landscapes for the conservation of birds: A general framework and specific recommendations for urbanizing landscapes. Restoration Ecology. 2001; 9(3): 280–292.
- 3. McKinney M. Urbanization, Biodiversity, and Conservation. Bioscience. 2002; 52(10): 883–890.
- 4.
Luniak M. Synurbization—adaptation of animal wildlife to urban development. In: Shaw WW, Harris LK, Vandruff L, editors. IUWS 2004: Proceedings of the 4th International Urban Wildlife Symposium.; 1999 May 1–5; Tucson, Arizona; Arizona: CALSmart; 2004. p. 50–55.
- 5. Lowry H, Lill A, Wong B. Behavioural responses of wildlife to urban environments. Biological Reviews. 2013; 88(3): 537–549. pmid:23279382
- 6. Chapman T, Rymer T, Pillay N. Behavioural correlates of urbanisation in the Cape ground squirrel Xerus inauris. Naturwissenschaften. 2012; 99(11): 893–902. pmid:23052820
- 7. Ditchkoff S, Saalfeld S, Gibson C. Animal behavior in urban ecosystems: Modifications due to human-induced stress. Urban Ecosystems. 2006; 9(1): 5–12.
- 8. Tsunoda M, Kaneko Y, Sako T, Koizumi R, Iwasaki K, Mitsuhashi I, et al. Human disturbance affects latrine-use patterns of raccoon dogs. Journal of Wildlife Management. 2019; 83(3): 728–736.
- 9. van der Vinne V, Gorter J, Riede S, Hut R. Diurnality as an energy-saving strategy: energetic consequences of temporal niche switching in small mammals. Journal of Experimental Biology. 2015; 218(16): 2585–2593.
- 10. Łopucki R, Mróz I, Berliński Ł, Burzych M. Effects of urbanization on small-mammal communities and the population structure of synurbic species: an example of a medium-sized city. Canadian Journal of Zoology. 2013; 91(8): 554–561.
- 11. Surov A, Poplavskaya N, Богомолов П, Kropotkina M, Tovpinetz N, Katzman E, et al. Synurbanization of the Common hamster (Cricetus cricetus L., 1758). Russian Journal of Biological Invasions. 2016; 7(1): 69–76.
- 12.
Franceschini C, Millesi E. Influences on population development in urban living European hamsters (Cricetus cricetus). In: Proceedings of the 11th meeting of the International Hamster Workgroup; 2003; Budapest, Hungary. 2003. p. 12–14.
- 13. Rusin M, Banaszek A, Mishta A. The common hamster (Cricetus cricetus) in Ukraine: Evidence for population decline. Folia Zoologica -Praha. 2013; 62(3): 207–213.
- 14. Kaim I, Hędrzak M, Ziewacz Ł. Daily activity pattern of the common hamster (Cricetus cricetus) at two localities situated in urban and rural areas. Zoologica Poloniae. 2014; 58(3–4): 59–69.
- 15. Čanády A. New site of the European hamster (Cricetus cricetus) in the urban environment of Košice city (Slovakia). Zoology and Ecology. 2013; 23(1): 61–65
- 16. Feoktistova N, Surov A, Tovpinetz N, Kropotkina M, Bogomolov P, Siutz C, et al. The common hamster as a synurbist: a history of settlement in european cities. Zoologica Poloniae. 2014; 58(3–4): 116–129.
- 17. O’Brien J. Saving the common hamster (Cricetus cricetus) from extinction in Alsace (France): Potential flagship conservation or an exercise in futility? Hystrix the Italian Journal of Mammalogy. 2015; 26(2): 89–94.
- 18.
Weinhold U. European Action Plan for the conservation of the Common hamster (Cricetus cricetus, L. 1758). 2009. Report No. 158, Affiliated to the Council of Europe, Nature and environment.
- 19. Ziomek J, Banaszek A. The common hamster, Cricetus cricetus in Poland: Status and current range. Folia Zoologica -Praha. 2007; 56(3): 235–242.
- 20. Roberge J, Angelstam P. Usefulness of the Umbrella Species Concept as a Conservation Tool. Conservation Biology. 2004; 18(1): 76–85.
- 21. Rutz C. The establishment of an urban bird population. Journal of Animal Ecology. 2008; 77(5): 1088–1019.
- 22. Siutz C, Valent M, Ammann V, Niebauer A, Millesi E. Sex-specific effects of food supplementation on hibernation performance and reproductive timing in free-ranging common hamsters. Scientific Reports. 2018; 8(1): 13082. pmid:30166598
- 23. Ziomek J, Zgrabczyńska E, Poradzisz A. The behaviour of the common hamster (Cricetus cricetus) under zoo conditions. Der Zoologische Garten. 2009; 78(4): 221–231.
- 24. Hędrzak M, Cywicka D, Kaim I. Comparison of localities of European hamster (Cricetus cricetus) in the areas of high and low level of human activity. Urban Ecosystems. 2018; 21(2): 323–338.
- 25.
Flamand A. Experimental introduction of common hamster in suburban areas: a worthwhile opportunity for conservation? A French example. Proceeding of the 25th meeting of the International Hamster Workgroup; 2018 October 4–6; Strasbourg, France. 2018. p 61–62.
- 26.
Siutz C, Pluch M, Ruf T, Millesi E. Sex Differences in Foraging Behaviour, Body Fat and Hibernation Patterns of Free-Ranging Common Hamsters. In: Ruf T., Bieber C., Arnold W., Millesi E. (eds) Living in a Seasonal World. Berlin: Springer; 2012. pp 155–165.
- 27. Siutz C, Millesi E. Effects of birth date and natal dispersal on faecal glucocorticoid concentrations in juvenile Common hamsters. General and Comparative Endocrinology. 2012; 178(2): 323–329. pmid:22732077
- 28. Górecki A. Energy flow through the common hamster population. Acta Theriologica (Warsz). 1977; 22(2): 26–66.
- 29. Barber J, Crooks K, Fristrup K. The costs of chronic noise exposure for terrestrial organisms. Trends in Ecology and Evolution. 2010; 25(3): 180–189. pmid:19762112
- 30. Siutz C, Franceschini C, Millesi E. Sex and age differences in hibernation patterns of common hamsters: adult females hibernate for shorter periods than males. Journal of Comparative Physiology. B, Biochemical Systemic, and Environmental Physiology. 2016; 186(6): 801–811.
- 31. Altmann J. Observational Study of Behavior: Sampling Methods. Behaviour. 1974; 49(3/4): 227–267.
- 32.
Schmelzer E, Millesi E. Activity patterns in a population of European hamsters (Cricetus cricetus) in an urban environment. Proceedings of the 11th meeting of the International Hamster Workgroup; 2003; Budapest, Hungary. 2003. p. 19–22.
- 33.
Niethammer J. Cricetus cricetus (Linnaeus, 1758)—Hamster (Feldhamster). In: Niethammer J, Krapp F, editors. Handbuch der Säugetiere Europas, Bd 2/I,Rodentia II. Mannheim: Akademisch Verlagsgesellschaft. Wiesbaden. 1982. p. 7–28.
- 34.
Ziomek J, Banaszek A, Nowak U, Walkiewicz A. Behaviour of the common hamster juveniles under natural conditions. In: Proceedings of the 19th Meeting of the International Hamsterworkgroup; 2012 November 20–22; Herkenrode Abbey, Belgium. 2012. p. 27.
- 35.
R Development Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing. Vienna, Austria. 2018. Available online at https://www.R-project.org/.
- 36.
Akaike H. Information theory and the maximum likelihood principle. In: 2nd International Symposium on Information Theory. In Petrov B, Csaki B, editors. ISIT 1973: Proceedings of the 2nd International Symposium on Information Theory; 1971 September 2–8, Tsahkadsor, Armenia. Budapest: Academiai Kiado; 1973. p.267-81.
- 37. Bates D, Maechler M, Bolker B, Walker S, Maechler Martin, Walker S. Fitting Linear Mixed-Effects Models Using lme4. Journal of Statistical Software. 2015; 67(1): 1–48.
- 38.
Burnham K, Anderson D. Model selection and multimodel inference: a practical information-theoretic approach. 2nd Edition. New-York: Springer; 2002.
- 39. Lenth R, Singmann H, Love J, Buerkner P, Herve M. emmeans: Estimated Marginal Means, aka Least-Squares Means. R Package Version 1.4.1. 2019 September 12. Available from: https://cran.r-project.org/web/packages/emmeans/index.html.
- 40. Feoktistova N, Meschersky I, Tovpinetz N, Kropotkina M, Surov A. A history of common hamster (Cricetus cricetus) settling in Moscow (Russia) and Simferopol (Ukraine). Beiträge zur Jagd- und Wildforschung. 2013; 38:225–33.
- 41. Hufnagl S, Siutz C, Millesi E. Diet composition of Common hamsters (Cricetus cricetus) living in an urban environment. Säugetierkdl. 2011. Inf.8: 69–78.
- 42. Evans J, Dall S, Kight C. Effects of ambient noise on zebra finch vigilance and foraging efficiency. PLoS One. 2018; 13(12): e0209471. pmid:30596692
- 43. Łopucki R, Perzanowski K. Effects of wind turbines on spatial distribution of the European hamster. Ecological Indicators. 2018; 84:433–436.
- 44. Magle S, Angeloni L. Effects of urbanization on the behaviour of a keystone species. Behaviour. 2011; 148(1): 31–54.
- 45. Francis C, Barber J. A framework for understanding noise impacts on wildlife: An urgent conservation priority. Frontiers in Ecology and the Environment. 2013; 11(6): 305–313.
- 46.
Surov A, Feoktistova N, Bogomolov P, Tovpinetz N. Distribution of the Common hamster in urban areas. Proceedings of the 21th meeting of the International Hamster Workgroup; 2014 November 14–16, Frankfurt & Gelnhausen, Germany. 2014.
- 47. MacWhirter R. Effects of reproduction on activity and foraging behaviour of adult female Columbian ground squirrels. Canadian Journal of Zoology. 1991; 69(8): 2209–2216.
- 48. Franceschini-Zink C, Millesi E. Reproductive performance in female common hamsters. Zoology. 2008; 111(1): 76–83. pmid:18023565
- 49.
Pflaum C, Millesi E. Inter- and intrasexual behaviour in male European hamsters. Proceedings of the 11th meeting of the International Hamster Workgroup; 2003; Budapest, Hungary. 2003. p. 15–8.
- 50. Quirici V, Castro R, Oyarzún J, Ebensperger L. Female degus (Octodon degus) monitor their environment while foraging socially. Animal Cognition. 2008; 11(3): 441–448. pmid:18214556