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The social life of Norway rats (Rattus norvegicus)
Manon K Schweinfurth
eLife · 2020 · Review · CC BY
Abstract
The Norway rat has important impacts on our life. They are amongst the most used research subjects, resulting in ground-breaking advances. At the same time, wild rats live in close association with us, leading to various adverse interactions. In face of this relevance, it is surprising how little is known about their natural behaviour. While recent laboratory studies revealed their complex social skills, little is known about their social behaviour in the wild. An integration of these different scientific approaches is crucial to understand their social life, which will enable us to design more valid research paradigms, develop more effective management strategies, and to provide better welfare standards. Hence, I first summarise the literature on their natural social behaviour. Second, I provide an overview of recent developments concerning their social cognition. Third, I illustrate why an integration of these areas would be beneficial to optimise our interactions with them.
Full text
From PubMed Central, U.S. National Library of Medicine, as current on Oct 24, 2026. Paragraph numbers are ours, so an answer can point at one.
Introduction
The Norway rat (Rattus norvegicus, hereafter referred to as rat) is one of the most abundant mammals with a nearly worldwide distribution. Today, almost all wild rats live in close association with humans, leading to various forms of adverse interactions. For example, rats are known to transmit diseases, destroy stored food and damage infrastructure by gnawing on wires or fundaments. Consequently, it has been estimated that rats cost only the US economy a minimum of two billion dollars each year. Furthermore, rats are predators that can be a threat to other species, especially when introduced to a new area. Thus, there has been a huge interest to control rat populations since mediaeval times (e.g., ).
Today, controlling rat populations is becoming ever more important since the human population grows with increasing speed and in 2030 it is expected that more than 75% of all humans will live in cities, which means that they most likely will live together with rats. Therefore, interactions with rats are likely to increase in the future, if the rat population control remains that ineffective. At the same time, population control must not induce unnecessary pain or suffering in rats. To reduce rat populations humanely and effectively, however, detailed knowledge on their individual behaviour and social interactions is needed.
Whereas wild rats are undesired in close proximity to humans, domesticated rats are more than welcome as pet rats in households, where approximately 100’000 lived in 2019 in the UK alone, and as laboratory rats in scientific institutes, where more than 20 million rats are used worldwide for research every year. The use of rats have led to key advances in various fields. The first described scientific experiment using rats as model organism dates back to the 1850s. Ever since, rats turned into one of the most important model organisms, resulting in over 350 different laboratory strains available today (http://www.rrrc.us/search/). In 2004, the full genome of one strain (BN/SsNHsd) was sequenced, which further increased the possibilities of research in the fields of biochemistry, genetics, genomics and physiology. Today, it has been estimated that worldwide approximately one study is published per hour that used rats as model organism.
The use of any non-human animal species in research raises ethical issues, concerning under which conditions humans are allowed to use and potentially harm them. Moreover, it has been pointed out that poor welfare can impact the quality of science and may hence be one factor of the reproducibility crisis in science. In order to provide optimal handling and care and identify factors inducing potential harm and pain, detailed knowledge on the rat’s social needs are essential.
Given their omnipresence and close association with humans, it is surprising how little is known about the rats’ individual social behaviour under natural conditions. One reason for this shortcoming is that rats as nocturnal and sub-terrestrial animals are notoriously difficult to observe. Despite these challenges, there is the general assumption that wild rats are not being particularly prosocial towards their conspecifics (e.g.,;; ). This stands in stark contrast to recent laboratory studies showing that rats are highly social animals that depend strongly on conspecific cooperative interactions and consequently show elaborate prosocial behaviours, such as freeing trapped partners and exchanging favours.
These different conclusions about the social behaviour of rats are surprising and require further investigations. One possibility is to compare the different lines of research on domesticated and wild rats. Since domestication of rats has started in the 19th century, it is sensible to assume that selective breeding and adaptions in response to artificial environments occurred and hence wild rats differ from domesticated rats in their social behaviour. Furthermore, wild rats have the propensity to rapidly adapt to environmental changes. In accordance, direct comparisons between the behaviour of wild and domesticated rats show that, for instance, wild rats burrow less, are more neophobic, learn more slowly and are more aggressive towards conspecifics. Consequently, wild rats dominate domesticated rats in direct interactions. However, the described differences between wild and domesticated rats are rather quantitative than qualitative (Figure 1). Indeed, domesticated rats show the full behavioural repertoire of wild rats. Consequently, domesticated rats have been shown to survive and reproduce under semi-natural conditions, even if predators were present. Thus, the behaviour of domesticated and wild rats can be representative for each other and hence the obtained knowledge on domesticated rats can inform studies on wild rats and vice versa. An integration of laboratory and field studies would therefore be highly valuable for all human interactions with this animal in general.
Aim of this review
Although few other vertebrates have a similar impact on humans as the rat, we know surprisingly little about their individual social behaviour in nature. Furthermore, their social cognition has been largely ignored in developing management strategies for wild rats or lab protocols and welfare recommendations for laboratory rats. This review is an attempt to rectify this problem. In the first part of this review, I provide a summary of the social structure and the individual social behaviour of rats, as far as it is known. In the second part, I then review recent developments on the social skills of rats, mostly performed under controlled laboratory conditions. Finally, I elaborate on why an integration of both research lines would be desirable.
Social behaviour of wild rats
Wild rats live almost exclusively in close contact with humans. Still, knowledge of wild rats is almost exclusively based on a few early pioneering studies, which have rarely been pursued because formerly used methods are not considered ethical or safe enough anymore. Still, there are more recent studies that tested either wild-derived rats, that is laboratory-reared descendants of wild rats, or wild-caught rats in captivity. Here I aim at synthesising this body of literature, which has not been recently reviewed in the light of the rat’s social life, to make the information easily accessible to those working with rats. Given the new developments in the field of social cognition, a comprehensive review on the natural social behaviour is needed to align the disciplines and potentially inform each other. Throughout, I highlight the potential of more research on their social life for future research in various disciplines.
The social structure
Wild rats live in large colonies, which, dependent upon food resources, may be composed of more than 150 individuals. Colonies are usually structured into subgroups, which might consist of pairs, harems with or without offspring, unisexual groups and/or single males and females. Although wild rats frequently interact with other colony members, it is unclear how often they interact with members of different subgroups and how stable such subgroups are. Answers to such questions will greatly inform management strategies, by e.g. assessing which rats are likely to learn food avoidances or encounter contaminated faeces, and validate fundamental research, by e.g. investigating often made assumptions about the frequency of social interactions.
Wild rats jointly excavate a burrow system, which consists of tunnels and chambers that serve as shared nest sites as well as places for food storage. Since behavioural data is mostly lacking, it is unknown whether rats have task differentiation, e.g. digging, defending, or scanning the environment for predators. Outside their burrow, rats establish a trail system, which is marked by olfactory cues and serve as foraging paths as well as connections between sites. A schematic overview of the social structure of a rat colony is provided in Figure 2.
Differential relationships
The social relationships between colony members can be highly variable. Studies on wild rats under semi-natural conditions showed that while mothers form strong bonds with their infants until these are around two months old, there is no evidence that adult wild rats form stable pair bonds (e.g.,; ). In line with this, wild-derived females also do not form selective social bonds in captivity. The lack of pair and social bonds is intriguing and stands in contrast to many other social mammals. Why rats show many social behaviours (see ‘Social cognition in rats’), but do not integrate social information into bonds deserves further investigation in order to elucidate their social activities with implications for housing recommendations.
What seems more important than bonds is an organisation based on dominance hierarchy. Probably based on their oestrus cycle, female rats form rather loose hierarchies under captive (domesticated and wild rats:; wild-derived: ) and semi-natural conditions. Under the latter conditions, males form more pronounced, stable and near-linear hierarchies based on fighting abilities. Three main male types have been identified: Alpha males are the largest individuals in the colony, move freely and initiate attacks on intruders. Beta males shy away from alpha males but can gain weight. Lowest ranking omega males generally lose weight and do not reproduce. Therefore, omega males often disperse from their natal colony. The dominance hierarchies in rats are characterised and maintained by the exchange of various social behaviours (summarised in an ethogram, Table 1).
Agonistic behaviours
Studies on wild rats under semi-natural conditions showed that overt aggression between colony members occurs infrequently. Instead, most agonistic behaviours are directed against intruders from outside the colony. This might explain the comparatively low dispersal rates in wild rats. In general, males seem to be less socially tolerant than females. Hence, solely males patrol and defend the territory boarders. Females, in contrast, seem to be less territorial, but defend their breeding chamber when lactating. Although domesticated rats are known to kill conspecifics under limited space conditions in the laboratory (e.g., ), there is no evidence that rats kill each other under natural conditions, in which there is enough space for separation. It is possible, however, that rats evict others from the colony, resulting in evicted rats being prevented from feeding and facing an increased risk of predation, which may ultimately lead to the death of the evictees.
Factors that increase conspecific aggression and therefore decrease social harmony are of particular interest for welfare recommendations and management strategies. Providing an adequate social environment with minimal aggression for animals in captivity is important and challenging likewise. The same conditions should be avoided where they are undesired to prevent rat populations to grow. Although domesticated rats show lower levels of aggression compared to wild rats, they show the same repertoire of aggressive behaviours. Hence, findings from wild and domesticated rats can reciprocally inform each other to understand how, for instance, group stability, partner choice, population density and physical environment (e.g., nesting possibilities and food distribution) can influence aggressive competition and social stress, which can be incorporated in welfare and management recommendations.
Grooming and other affiliative behaviours
Rats engage in affiliative behaviours in various situations. A frequent affiliative behaviour in wild rats is allogrooming, where one individual licks or nibbles the fur of a conspecific. In wild-derived female rats such allogrooming is directed preferably to spots that are difficult to reach for the groomed individual, such as the face or neck. Wild rats experience such grooming already early in life, as it is directed from mothers towards infants. Later, infants transfer this behaviour to other colony members. Comprehensive data on the occurrence of this probably most important social behaviour in the wild is missing since it usually takes place invisibly underground. Hence, it is not known how much time wild rats spend allogrooming, in which situations they show allogrooming, and whether there are additional functions to hygienic reasons, as shown in primates. Such information has important implications for management protocols, because it allows predictions about the spread of diseases. It is also important for welfare recommendations, as it allows meaningful comparisons between the social behaviour of captive and free-living animals, which is called behavioural integrity.
Other affiliative or beneficial behaviours include food sharing, huddling and pioneering. As wild rats share the same feeding sites, some colony members share food with others either by allowing them to take food or by letting them lick off residues from their fur. Huddling, where rats lie together piled in a heap on top of each other, is beneficial for thermoregulation and thus, common amongst altricial infants (domesticated rats:;; wild rats: ). Moreover, adult rats huddle together, even under warm conditions and when there is ample opportunity to separate, which suggests some social function beyond thermoregulation. When pioneering, one rat vigilantly leaves the burrow and observes the surroundings for several minutes. Only then will other colony members appear from the burrow as well. This behaviour is likely to be beneficial for colony members that stay in the burrow until the pioneer has scanned the environment for potential dangers.
Play behaviour
Another socio-positive behaviour, which is mostly shown by young rats, is social play. Generally, social play behaviour is common among young animals as being part of the process of learning adult behaviour. Although wild rats have been reported to play with each other (, p.180; ), most evidence of social play is based on work on domesticated rats (reviewed in: ). Domesticated rats engage in play fights, so-called rough-and-tumble play, when they are about 17 days old and retain this behaviour until they reach sexual maturity. During play fights, young domesticated and wild-derived rats wrestle, box and kick each other in order to turn the opponent on the back and attack the nape. The same study found that wild-derived rats show less social play compared to domesticated rats and their play involves less body contact. Domesticated rats emit 50 kHz calls during such play, which are associated with positive emotions and hence point towards rewarding effects of social play. Studies on the neurobiology of this naturally rewarding behaviour can inform, for instance, research on human reward systems and psychiatric disorders. Given that rats are a better model organism for such disorders than mice and effort in developing treatments is increasing, research in rats is predicted to increase in the future likewise. To differentiate abnormal from normal behaviour and to establish a meaningful model, comparative studies under natural conditions are crucial.
Reproductive behaviour
Wild rats reach sexual maturity at an age of two to three months. Both sexes are highly promiscuous, and males are usually not able to monopolise single females due to the presence of many other males in the colony. Furthermore, compared to other mammals, wild females have a short oestrus cycle of one to two weeks, which is further reduced to only four days in domesticated rats. Like other domesticated animals, domesticated males have been selected for increased fecundity and thus show also enlarged testes and reach maturity earlier than wild rats.
There is not much evidence for mate choice in wild rats. When living in large groups, several males follow the receptive female during their short receptive period before copulation. Most of the males successfully copulate with the female repeatedly. After ejaculation, domesticated male rats in the laboratory insert a vaginal plug, which dissolves after 12 hr, but so far there is no evidence for these plugs in wild rats.
Clearly, the rapid breeding of rats is one of the reasons for their success. Detailed knowledge on their reproductive behaviour in the wild, for example factors that promote or supress it, is needed to either prevent reproduction in the wild or promote reproduction in the laboratory. For instance, pregnant laboratory females resorb their embryos, if they smell cat urine in their nest during the first third of gestation. This could be a non-invasive tool to discourage and prevent wild rats from nesting and breeding. Furthermore, contraception and contragestion as management tools have been recently revisited mainly because they are non-lethal. Importantly, mathematical models showed that such fertility control methods can be as effective as more traditional methods, such as baiting and trapping. Still, reproduction in the wild is understood only very little.
Mother-infant behaviour
Approximately three weeks after copulation, females give birth to a litter of four to eight pups in wild rats and eight to sixteen pups in domesticated rats. Whereas domesticated rats breed communally under laboratory conditions (e.g., ), this has not been confirmed under natural conditions. Here, pups are born in a private underground chamber of the communal burrow. Males show no paternal care, whereas females nurse the altricial offspring until weaning at approximately 40 days. Thereafter, the offspring stays in close association with their mother for up to two months, which stands in contrast to the common practice of breeders to separate offspring from their mother at the age of three weeks.
Maternal behaviour has profound long-term effects on offspring through changing their epigenome, which has been extensively studied in laboratory rats (reviewed in;;;; ). For instance, offspring of highly attentive mothers, which intensively lick and groom their offspring, show low plasma corticosterone levels, modest stress responses, better spatial learning, increased memory and become attentive mothers later in life, too. These maternal effects can affect biomedical research outcomes. If drugs are developed using rats that were raised by less attentive mothers or were separated from their mothers for even short periods, the sample will show significant behavioural and neurological changes (e.g., ). Resulting drugs might only be effective and transferrable to humans that have also had faced considerable stress. Furthermore, elevated stress levels raise welfare issues in these animals. To establish what good maternal care means and associated variation, comparisons with wild rats in their natural habitat are indispensable.
Social cognition of rats
Groups of wild rats are socially complex as they live in long-term groups of multiple generations, which allows for repeated interactions with differently familiar and related individuals (see for the characteristics of social complexity). Their complex social system implies that rats need certain cognitive adaptations to deal with challenges like mate or food competition that can be overcome, for instance, by cooperation or social learning. Yet, the social system of rats does not allow general conclusions about the underlying cognitive mechanisms of their behaviours. In recent years, there has been a considerable interest in understanding cognitive and emotional mechanisms of (mostly domesticated) rats when interacting with conspecifics. However, this recent development has not yet been aligned with the rat’s natural social environment. Hence in the second part, I elucidate the socio-cognitive skills of rats, which have mostly been studied under controlled laboratory conditions, to highlight the rat’s high social and emotional abilities.
Recognising others
Recognising others is an important skill for almost all social behaviours. Recognition might be based on learning cues of familiar individuals or differentiating between classes, e.g. kin from non-kin. Both can be of relevance in mate choice, hierarchy formation or brood care. Indeed, rats distinguish not only between kin and non-kin (domesticated rats:;; wild-derived rats: ), but also between different degrees of relatedness on the level of cousins (domesticated rats: ). This ability is probably the result of prenatal imprinting, as rat pups prefer the amniotic fluid of their mother, even if they were born by Caesarean section. In addition, wild rats are able to discriminate colony members from intruders. Remarkably, domesticated rats can truly differentiate between single conspecifics based on individually distinct odour cues after they were given the opportunity to learn such cues, instead of just using familiarity based heuristics. This ‘true individual recognition’ is assumed to be cognitively challenging and has been demonstrated in only few other animal species.
Emotion reading
Besides being able to identify others, domesticated rats are also capable of assessing the emotional state of other individuals, allowing them to predict future behaviour. This includes a differentiation of whether another individual is, for example, in a playful or aggressive mood. Rats show a large repertoire of facial expressions, which are used to evaluate emotional states of conspecifics. Furthermore, they collect information of emotional states by odour cues from urine, which signal if another individual is stressed or frustrated. These results highlight how sensitive rats are to the emotional states of conspecifics. The underlying mechanism of such emotion reading, however, is not yet clear. Rats may respond to certain emotions either by learned associations or alternatively by emotional contagion.
Emotional contagion
Emotional contagion means sharing the emotional state with another individual. It is expressed by mimicking or being influenced by the response of other individuals. This qualifies as a basic form of empathy without a cognitive understanding of another individual’s feelings. Indeed, it is assumed to represent the oldest form of empathy in evolutionary terms, being present in many animal species, including humans. Emotional contagion serves an important adaptive value, that is saving time and energy by copying others instead of assessing and evaluating situations independently. There is ample evidence that rats are capable of showing emotional contagion. When familiar with a particular stressor, domesticated rats stop moving, if realising that other individuals are experiencing this stressor. Furthermore, if rats previously experienced electro-shocks for certain actions themselves, they stop pressing a self-rewarding lever, if they observe a partner being electro-shocked for their action. Finally, rats learn to avoid situations that are harmful to others, even if they never experienced the harmful situation themselves (e.g., ). Thereby it is not necessary for them to observe the behaviour of other rats because the smell of a stressed conspecific’s urine can elicit a stress response.
Helping behaviour
Rats not only use the knowledge about another individual’s emotional state for themselves, but also incorporate this knowledge to help conspecifics (summarised in Table 2). Rats have a high motivation to help each other, exemplified by their preference to cooperate, even if it is possible to achieve the same reward individually. For instance, domesticated rats can coordinate their behaviour with conspecifics to avoid electric shocks or to gain rewards for themselves and their partner. Such coordination for a mutual benefit is independent of sex, strain or familiarity between the test animals. However, rats housed in isolation are not able to coordinate their behaviour with conspecifics, suggesting the social environment being necessary in developing social skills. When given the choice between delivering a reward to either themselves only or also to a partner at no cost, domesticated rats opt for the latter mutually-rewarding option. This consistent finding is surprising given that many other animals, including non-human primates, show only inconstant or limited evidence for helping conspecifics at no cost in similar prosocial choice tasks (reviewed in ).
Rats help conspecifics in several situations. For example, domesticated and wild-derived rats help each other by grooming spots that are difficult to reach by their own. Furthermore, rats warn colony members by producing alarm calls in the 20 kHz range (see 'Communication as a mean to mediate social behaviour'), to which conspecifics respond either by slowing down their movement or by fleeing into their shelters. Domesticated rats in semi-natural enclosures are more likely to call in the presence of colony members, which suggests that the call is not a mere by-product of predator presence. However, a more recent laboratory study did not find that alarms calls were elicited more often in presence of conspecifics, which deserves further investigations of the mechanisms underlying alarm calls in rats.
In addition, domesticated rats have a high propensity to help trapped partners by opening a door of a restrainer (e.g.,;; ). This cannot be explained by mere curiosity to manipulate the door because rats preferably release familiar partners over strangers. In addition, the results are unlikely to be explained by seeking social contact as rats free trapped partners even if social contact is prevented and rats only free partners when they are stressed. Furthermore, if treated with an anxiety-reducing drug, they release trapped partners less often, potentially because of reduced sympathy for the trapped partner. Taken together, rats adjust their help, which might be based on empathic concerns.
Moreover, domesticated and wild rats have been shown to spontaneously share food with others, even if they have the chance of consuming the food on their own. Food donations are fine-tuned to the partner’s need to receive help, which may be communicated visually, acoustically or as a combination of several cues. In summary, wild, wild-derived and domesticated rats help each other readily in various contexts, suggesting that, rats are highly cooperative at least in captive settings.
Reciprocal interactions
When rats share food, they reciprocate help, that is they base their decision to provide food on previously received donations and pay back quid pro quo. More specifically, rats use at least two reciprocal rules. The rule ‘I help you because someone helped me’, that is generalised reciprocity, is followed by female, but not male wild-derived rats. In addition, when interacting with the same partner repeatedly, rats use direct reciprocity, that is ‘I help you because you helped me’ (domesticated rats, wild-derived rats). Thereby, they not only take into account whether the partner has helped them in the past, but also the quality of received help and the eagerness of the partner to provide help.
While experimental laboratory studies on reciprocal food donations are inevitable to rule out alternative explanations, they have been criticised on the basis of their artificial design and involved training. To demonstrate their biological relevance, it is therefore necessary to show similar patterns also in naturally occurring behaviours that do not require any training. Two recent studies showed that wild-derived rats also exchange natural occurring allogrooming reciprocally. While allogrooming is a rather short affiliative behaviour, the reciprocal exchange has important life-long consequences, as rats that allogroom partners reciprocally live longer and develop fewer mammary tumours. Further, rats exchange food in an artificial setting against allogrooming as a natural behaviour. This shows that artificial tasks can be suitable means to study reciprocity and that rats follow sophisticated rules when interacting with each other, which cannot be explained by training.
Social learning and culture
Rats do not only benefit from conspecifics of which they receive help, but they also gain important information from others, for example about toxic diets or hunting techniques. They use this information even if it conflicts with their personal information. Learning to avoid certain diets has led to an arms race between the development of new poisons and the ability of wild rats to avoid these. When learning from others where to eat, wild and domesticated rats employ various methods (reviewed in ). First, they show local enhancement, that is visiting food locations where other rats were observed. Second, locations can be communicated by urine markings, which are used by others to locate suitable feeding sides. Third, already before eating solid food, domesticated rats learn from their mother which food is palatable due to diet cues in the maternal milk. Finally, domesticated adult rats can learn to copy preferences of other rats, which can be based on the breath of conspecifics. The so acquired preferences, learned over few encounters only, can last for at least one month.
Socially learned and transmitted information can result in group-specific behavioural patterns, shared by members of a community. Such patterns are commonly referred to as culture. Indeed, wild rats show local differences in their hunting techniques that appear to fulfil the definition of culture. These local hunting traditions include raiding bird nests, hunting for birds up to the size of ducks, fishing for small fish and diving to collect mussels.
Social knowledge
Rats have been repeatedly shown to learn from conspecifics (see 'Social learning and culture'). They also observe others to infer information indirectly through transitive inference. This is particularly important in near-linear dominance relationships. For example, if an individual A is dominant over individual B and B over C, one can conclude that A might be dominant over C, even if this relationship was not directly observed. Domesticated rats can logically infer about hierarchical relations in artificial tests: but see also, highlighting their socio-cognitive abilities.
Communication as a mean to mediate social behaviour
Social interactions generally involve some form of communication, that is the intentional transfer of information between two individuals. Rats are known to use visual, acoustic and olfactory cues for communication. As rats are active mainly at dusk and dawn, their visual system is poorly developed compared to diurnal mammals. Accordingly, visual communication plays only a minor role during social interactions relative to other sensory modalities.
Rats communicate acoustically, both within and above (>20 kHz) the human frequency range. Audible for humans is the defeat cry, which is directed to con- and heterospecifics. Mostly, however, rats communicate within the ultrasonic range. This has been shown mainly in laboratory animals, without too much information on ultrasonic communication in wild rats. Three main ultrasonic calls have been described in domesticated rats: an alarm call (frequency: 22 kHz, length: 300–3,000 ms), a social call (50 kHz, 20–80 ms) and an isolation call (40 kHz, 80–140 ms). While the former two types are emitted by adults and juveniles alike and occur in a variety of contexts, the latter are produced only by juvenile rats when they are separated from their litter or mother. Social calls commonly are produced in a socio-positive context, that is during social play, joint exploration, cooperation and during copulations, as they may lead to approach behaviours by others. In contrast, alarm calls are usually associated with socio-negative contexts, that is when being threatened by predators, being exposed to fearful situations, showing submissive displays, but also during copulations. Although fluctuation around 22 kHz, pitches of alarm calls differ across contexts, suggesting context specific modulations.
Besides communicating vocally, rats also transfer information via odours (reviewed in; ). Such odour cues are used in a variety of contexts. First, domesticated rats actively scent mark objects or surfaces using urine or faeces by pressing their anogenital area or rubbing their flanks over the respective surface, possibly to signal dominance. In wild rats, both sexes leave such marks probably for the same reasons. Furthermore, they mark the paths outside their burrow to optimise foraging efficiency and to increase protection from predators by using them as escape paths. In addition to urine, faeces are preferentially dropped at latrines or at places where rats of different colonies deposit urinary marks. This may suggest, that these areas serve as information centres. Rats also possess glands across their body, whose odours transfer information of relatedness and individual identity.
Potential applications
Thus far, this review illustrated that the social system of rats is highly complex, both in the wild and in the laboratory. Rats form large socially structured colonies in the wild and exhibit various sophisticated social skills in the laboratory. Still, the inherent value of information on their social behaviour and their sophisticated social skills have not been acknowledged enough in welfare and management recommendations. Furthermore, current research on domesticated rats is often decoupled from information on their natural life and research on wild rats is decoupled of information on their social cognition, although such an integration could greatly inform each other. Hence in the third part, I discuss potential applications and future directions of such knowledge in different fields.
Population management
Despite huge effort, controlling large rat populations has been mainly ineffective, especially in urban areas. Possible reasons include bait/trap avoidance and recolonization of patches of which rodents were removed.
Trapping rats is notoriously difficult, exemplified by the fact that it took a team of several researchers 18 weeks to capture a single individual on a small island, although this animal was equipped with a radio collar. Reasons for this considerable trap-shyness are elusive. Here, behavioural studies could help identifying the reasons for their trap-shyness. For instance, some personality types might be more prone to be trapped than others. Thus not all animals are equally well trappable, which will eventually lead to selection for trap-shyness, making future interventions more difficult. In addition, individuals might socially learn to avoid traps. Especially, their capacity for emotional contagion might be responsible for a strong negative association with traps. While new traps have been designed and their efficiency been evaluated, the design should also consider welfare aspects. In 7% to 14% of all cases, traps do not kill the rats but injure them, causing ethical issues.
One of the most important aspects in controlling rats is to prevent them from recolonization a newly available habitat. Understanding the dispersal of rats and their attraction to certain habitats is necessary to successfully prevent them from recolonizing a cleared patch. However, thus far we know very little about how rats decide where, when and under which circumstances they start building a burrow. It should be noted that especially the social life of urban rats, although causing the most problems, is the least understood. This is problematic because environmental factors strongly influence social and population dynamics in many animal species (e.g.,;; ) and urbanization has profound effects on many species. Hence, the generalisability of social structure and immigration levels obtained from rats living in other habitats, e.g. farms, is currently unclear.
Finally, the killing of any animal causes an ethical conflict and information about the rat’s social behaviour might enable the development of new methods to pre-emptively repel them or hinder their reproduction, which is considered most effective by control professionals. In addition, there is great demand for such strategies especially from organic farmers who aim to avoid rodenticides. Studying the rat’s mating behaviour might provide information on how to prevent or disrupt mating. Studying their nest-building behaviour might enable us to create unsuitable habitats targeted to rats. Furthermore, by increasing aggression between rats and decreasing social harmony, e.g. by blocking their communication, rats could be repelled.
Research in Animal Behaviour and Psychology
Research on the rat’s behaviour and psychology has been mostly conducted under laboratory conditions, which comes with assets and drawbacks. While rigorous experiments under controlled conditions are indispensable when scrutinising possible mechanisms of behaviours, such tests may not be relevant in the rat’s natural world due to, for example, reduced attention or motivation. Thus, it is unclear whether observed patterns under laboratory conditions play an important role in the natural life of rats where they face various challenges, such as predation, hunger, competition or illness. That said, any skill discovered even in the absence of a seemingly biological relevance at present is of fundamental interest, as it needs to be addressed why they might possess this skill.
In order to produce generalizable scientific outcomes, various techniques can be applied. First, experiments in the laboratory can be designed to simulate naturally occurring tasks, such as by providing semi-natural conditions. Second, field studies may pose questions that have so far not been investigated and are thus a highly valuable resource to design laboratory tasks that investigate mechanisms of real-world problems. Third, experimental research can be conducted in the field using novel techniques (see 'Future directions'). Thereby large samples can be studied in an ecologically relevant environment. Finally, interactions and collaborations between researchers studying rats in the laboratory and field will enhance external validity by combining expertise, of which this review is an attempt.
Research in Biomedicine, Neuroscience and Pharmacology
Virtually all medical achievements have involved animal experiments at some stage, especially with rodents. Choosing the best possible model organism for a test to measure what it claims to be measuring is the basis for the success of such studies. Yet, test validity cannot be assessed without detailed information of rats in their natural environment and their cognitive and emotional skills.
Every species evolved by adapting to a certain ecological niche, which has important consequences for biomedical research. If rats are tested in situations or with stimuli that do not resemble their ecological and social environment, they may not show an adaptive response, which might be different than that of humans in the same situation. Therefore, a direct comparison might be difficult. Even if naturally occurring stimuli are used, the frequency, duration and intensity of the stimuli should be closely matched to the natural situation to observe adaptive behaviour. Studies of rats in their natural environment would help to inform biomedical research to design ecological relevant and translatable studies. This can be illustrated for research on stress responses. Rats have been traditionally given stressors that are arbitrary and artificial, like foot shocks, and their coping response is difficult to interpret. However, stressors that elicit the highest plasma corticosterone responses are not artificial and involve social situations with conspecifics, like social defeat. The natural history of rats can inform us about the predictability, duration and frequency of such events, different natural coping strategies and the natural variation therein.
Furthermore, some areas of biomedical research, for example neuroscience, enhance our understanding of mechanisms underlying abnormal behaviour. Often comparisons between normal and abnormal behaviours are necessary to identify and treat the latter. Such comparisons are only meaningful, if the control group is healthy and shows normal behaviour. Still, we mostly lack information about the rat’s ‘normal’ behaviour and individual variation of it, let alone information about naturally occurring abnormal deficits. In comparison to laboratory rats, wild rats live in a much more complex and variable social and physical environment. For example, wild rats build and live in large underground burrows where they interact with up to 30 times more group members than rats in captivity. Furthermore, group composition and size change regularly. Laboratory rats deprived of a complex environment show behavioural, neurobiological, physiological and psychological changes (reviewed in;;;; ). This questions whether rats in control group show ‘normal’ behaviour and whether they are therefore a valid comparison to healthy humans. Thus, studies are needed that compare laboratory with wild rats to fully assess ‘normal’ behaviour and physiology. In addition, different captive settings should be explored where rats do not develop abnormal behaviour or physiology. This should include enriching their social life in captivity, for instance by housing them in large mixed-sex groups, which would at least partly resemble their natural social life.
Finally, restrictive standardisations has led to the testing of small subsamples, of which conclusions are hardly transferable to the whole human population (reviewed in ). Test animals usually represent a homogenous group that is typically young, inbred and male. Moreover, test animals live in a restricted social and physical environment and share the same rearing and housing background. Findings obtained under such conditions are difficult to interpret because neither rats in other laboratories, nor in the wild, nor humans face similar restrictions. Keeping rats under more diverse settings would mitigate this problem.
Animal welfare
Scientific insight is only meaningful, if it is based on valid, reliable and repeatable experiments. All of these essential features of science can be reduced by poor welfare of the test animals (reviewed in ). In addition, there is increasing public concern about animal welfare in scientific studies. This is reflected, for instance, in animal right movements, animal protection organisations, constantly improved legislation and the development of animal ethics committees. Today, 75–100 million vertebrates are used in scientific studies per year, one third of which are rats. Given this magnitude, the ethical treatment of rats in research is an important social issue.
Fundamental aims of good welfare include the animals’ well-being and positive emotions. Whereas most work has been done to improve the physical environment of laboratory animals, enhancing their social environment has received less attention. Many studies have shown that isolated rats develop depression-like behaviours (e.g.,; ). Their great social need is highlighted by the fact that rats prefer spending time with a conspecific over receiving heroin or methamphetamine, even if they are addicted to these substances. They also put more effort in joining familiar conspecifics than inanimate objects or larger cages. Finally, isolated rats showed marked differences in their behaviour, cognition, physiology and neurobiology that is likely to impact the translatability of results obtained on such animals. All these studies present a strong case for housing rats socially.
However, social partners do not only provide comfort and entertainment, but can also cause stress and injuries. For instance, peer rejection during adolescence has been shown to have long-lasting effects in the brain and social behaviour of rats. Therefore, it is crucial to house rats with appropriate partners, which has so far been largely neglected. Studying rats in the natural environment, in which they evolved, could give insights into individual interaction patterns as a function of space or disruptions of social dynamics and their resolution. Furthermore, we need to better understand causes of induced stress and aggression in wild rats to eliminate or reduce such factors in captivity. Severe physical attacks are risky and are thus usually avoided. However, early isolation from mothers might lead to poor social competencies and limited hiding opportunities might lead to escalations between individuals of similar ranks or unfitting personalities.
In addition to social housing, recent findings on the social skill set of rats should be incorporated in handling and experimenting protocols. Rats realise and respond to conspecifics that are stressed or in pain (reviewed in ). For example, rats that interact with a familiar partner in pain show afterwards stronger pain reaction themselves compared to rats that interact with an unfamiliar partner in pain. Rats have been shown to possess mirror neurons that are active when experiencing pain and when observing a conspecific in pain. At the same time the presence of a partner can have buffering effects as rats seem to be less stressed when exposed to a stressor when in company of a cage mate or when they can interact with a social partner shortly after a stressful event. In line with this finding, experiencing stressful situations together with a cage mate leads to a lack of fear conditioning towards such stressors, which might be important for experiments that are based on repeated treatments.
Chronically stressed laboratory animals are more likely to become aggressive, as well as physically and mentally sick. This creates an unsafe environment for caregivers and can lower the generalisability of results. Knowledge on the cognitive and emotional skills of rats can be used to help rats to cope with stressful events. In addition, a detailed ethogram of wild rats can enable us to differentiate normal from abnormal behaviour, which is a very easy and non-invasive and way to assess the welfare of an individual and to make informed welfare recommendations.
Finally, a largely neglected welfare issue, but maybe an even more critical issue in terms of the affected numbers of rats, is the world-wide killing of enormous numbers of rats each year for population management purposes. Exact data on the number of killed rats is not available, besides an estimation of several million rats that were killed in the 90 s every year in the UK alone (reviewed in ). The currently available and legal control techniques can cause severe welfare issues. Poisoning, especially with anticoagulants, is the easiest, most effective and most common way of controlling rat populations. However, it is also the least humane way because it interferes with the rat’s ability to forage or escape predators, leaves sub-lethally poisoned individuals ill, affects non-target species (including children) and causes long-lasting discomfort and pain in poisoned and conscious individuals over an average period of 7.2 days. Furthermore, rat pups may die of dehydration or starvation, if their mother is killed and the distress through emotion reading and emotional contagion in colony members, which observe individuals in pain, is hard to assess. Systematic observations of rats when control procedures are applied in addition to knowledge about their social skills are needed to fully assess the impact of a particular procedure for developing recommendations. Furthermore, the development of contraceptive drugs, such as 4-vinylcyclohexene diepoxide, seems a promising alternative because they are neither lethal nor toxic. Given that rats help others in need, read other’s emotions as well as feel with and potentially for each other, it is time to revisit and develop humane population control techniques that work pre-emptively.
Future directions
Important questions about the social life of rats under natural conditions have not been addressed. While more detailed field studies would be highly valuable, it is notoriously difficult to study rats under natural conditions. Rats are small nocturnal animals that are visible only shortly during dusk and dawn. For the rest of the day, they live in underground burrow systems. However, newly developed technology, such as small cameras, camera traps, pheromone-based lures, microchips or high resolution GPS tracking software have become available and affordable. In addition, guidelines have been developed how urban rats, which might transmit diseases, can be studied.
New research avenues to better understand the social behaviour of rats shall be taken by combining different disciplines. For example, given rats have an almost global distribution, this species would be ideal to study whether and how ecological factors influence their social behaviour, which can provide insights into the theory of social evolution. The gained knowledge on their behavioural ecology may inform comparative psychologists who study their social skills. By combining forces between pest control and behavioural studies, the gained information will shed lights on the individual behaviour of rats, which will inform humane population management projects. Three scientific disciplines, that is ethology, psychology and welfare have analysed the behaviour of rats for decades (e.g.,;; ). Merging their theories, methods and findings would greatly complement each other. In turn, the results of these disciplines may affect the ethical judgment of some currently used population control techniques.
References 257
- 1.
Abbott A. Return of the rat. Nature. 2009;460:788.
Not in our library10.1038/460788a
- 2.
Adams N, Boice R. A longitudinal study of dominance in an outdoor colony of domestic rats. Journal of Comparative Psychology. 1983;97:24-33.
Not in our library10.1037/0735-7036.97.1.24
- 3.
Akyazi I, Eraslan E. Transmission of stress between cagemates: a study in rats. Physiology & Behavior. 2014;123:114-118.
Not in our library10.1016/j.physbeh.2013.10.006
- 4.
Alberts JR. Huddling by rat pups: ontogeny of individual and group behavior. Developmental Psychobiology. 2006;49:165-171.
Not in our library10.1002/dev.20190
- 5.
Alberts JR, Galef BG. Olfactory cues and movement: stimuli mediating intraspecific aggression in the wild Norway rat. Journal of Comparative and Physiological Psychology. 1973;85:233-242.
Not in our library10.1037/h0035050
- 6.
Arakawa H. Ethological approach to social isolation effects in behavioral studies of laboratory rodents. Behavioural Brain Research. 2018;341:98-108.
Not in our library10.1016/j.bbr.2017.12.022
- 7.
- 8.
Austin OL. Predation by the common rat (Rattus norvegicus) in the cape cod colonies of nesting terns. Bird-Banding. 1948;19:60-65.
Not in our library10.2307/4510014
- 9.
Austin D, Dewsbury DA. Reproductive capacity of male laboratory rats. Physiology & Behavior. 1986;37:627-632.
Not in our library10.1016/0031-9384(86)90297-0
- 10.
Bailey NW, Moore AJ. Evolutionary consequences of social isolation. Trends in Ecology & Evolution. 2018;33:595-607.
Not in our library10.1016/j.tree.2018.05.008
- 11.
Barfield RJ, Auerbach P, Geyer LA, Mcintosh TK. Ultrasonic vocalizations in rat sexual behavior. American Zoologist. 1979;19:469-480.
Not in our library10.1093/icb/19.2.469
- 12.
Barnett SA. Behaviour components in the feeding of wild and laboratory rats. Behaviour. 1956;9:24-43.
Not in our library10.1163/156853956x00237
- 13.
Barnett SA. An analysis of social behaviour in wild rats. Proceedings of the Zoological Society of London. 1957;130:107-152.
Not in our library10.1111/j.1096-3642.1958.tb00565.x
- 14.
Barnett SA. The Rat - a Study in Behavior. 1963.
Not in our library10.1002/1098-2337(1976)2:2<164::aid-ab2480020210>3.0.co;2-m
- 15.
Barnett SA. Rats. Scientific American. 1967;216:78-85.
Not in our library10.1038/scientificamerican0167-78
- 16.
Barnett SA. The Story of Rats: Their Impact on Us, and Our Impact on Them. 2001.
Not in our library
- 17.
Barnett SA, Spencer MM. Feeding, social behaviour and interspecific competition in wild rats. Behaviour. 1951;3:229-242.
Not in our library
- 18.
Bartels DM, Hastie R, Urminsky O. Connecting laboratory and field research in judgment and decision making: causality and the breadth of external validity. Journal of Applied Research in Memory and Cognition. 2018;7:11-15.
Not in our library10.1016/j.jarmac.2018.01.001
- 19.
Bateson SP, Biggs P, Cuthbert A, Cuthill IC, Festing M, Keverne EB, King S, Page C, Petersen O, Rothwell N, Rushworth M, Walsh V, Roberts O. The use of non-human animals in research: a guide for scientists. The Royal Society. 2004;1-17.
Not in our library10.1177/026119290403200209
- 20.
Baumans V. Use of animals in experimental research: an ethical dilemma? Gene Therapy. 2004;64-66.
Not in our library10.1038/sj.gt.3302371
- 21.
Bekoff M, Byers JA. Animal Play: Evolutionary, Comparative and Ecological Perspectives. 1988.
Not in our library
- 22.
Ben-Ami Bartal I, Decety J, Mason P. Empathy and pro-social behavior in rats. Science. 2011;334:1427-1430.
Not in our library10.1126/science.1210789
- 23.
- 24.
Ben-Ami Bartal I, Shan H, Molasky NM, Murray TM, Williams JZ, Decety J, Mason P. Anxiolytic treatment impairs helping behavior in rats. Frontiers in Psychology. 2016;7:850.
Not in our library10.3389/fpsyg.2016.00850
- 25.
Berdoy M, Smith P, MacDonald DW. Stability of social status in wild rats: age and the role of settled dominance. Behaviour. 1995;132:193-212.
Not in our library10.1163/156853995x00694
- 26.
Berdoy M. The Laboratory Rat: A Natural History Oxford University: National Television System Committee. 2002.
Not in our library
- 27.
Berdoy M, Smith P. Arms race and rat race: adaptations against poisoning in the Brown rat. Ecological Reviews. 1993;48:215-228.
Not in our library
- 28.
Biro PA, Dingemanse NJ. Sampling bias resulting from animal personality. Trends in Ecology & Evolution. 2009;24:66-67.
Not in our library10.1016/j.tree.2008.11.001
- 29.
Blanchard RJ, Fukunaga K, Blanchard DC, Kelley MJ. Conspecific aggression in the laboratory rat. Journal of Comparative and Physiological Psychology. 1975;89:1204-1209.
Not in our library10.1037/h0077177
- 30.
Blanchard RJ, Flannelly KJ, Blanchard DC. Defensive behavior of laboratory and wild Rattus norvegicus. Journal of Comparative Psychology. 1986;100:101-107.
Not in our library10.1037/0735-7036.100.2.101
- 31.
Blanchard RJ, Flannelly KJ, Blanchard DC. Life-span studies of dominance and aggression in established colonies of laboratory rats. Physiology & Behavior. 1988;43:1-7.
Not in our library10.1016/0031-9384(88)90089-3
- 32.
Blanchard RJ, Blanchard DC, Agullana R, Weiss SM. Twenty-two kHz alarm cries to presentation of a predator, by laboratory rats living in visible burrow systems. Physiology & Behavior. 1991;50:967-972.
Not in our library10.1016/0031-9384(91)90423-l
- 33.
Blanchard RJ, Blanchard DC. Antipredator defensive behaviors in a visible burrow system. Journal of Comparative Psychology. 1989;103:70-82.
Not in our library10.1037/0735-7036.103.1.70
- 34.
Boice R. Some behavioral tests of domestication in Norway rats. Behaviour. 1972;42:198-230.
Not in our library10.1163/156853972x00275
- 35.
Boice R. Domestication. Psychological Bulletin. 1973;80:215-230.
Not in our library10.1037/h0034893
- 36.
Boice R. Burrows of wild and albino rats: effects of domestication, outdoor raising, age, experience, and maternal state. Journal of Comparative and Physiological Psychology. 1977;91:649-661.
Not in our library10.1037/h0077338
- 37.
Boice R. Behavioral comparability of wild and domesticated rats. Behavior Genetics. 1981;11:545-553.
Not in our library10.1007/bf01070009
- 38.
Booy O, Cornwell L, Parrott D, Sutton-Croft M, Williams F, Vilà M, Hulme P. E. Impact of biological invasions on infrastructure. Impact of Biological Invasions on Ecosystem Services. 2017;235-247.
Not in our library10.1007/978-3-319-45121-3
- 39.
Boreman J, Price E. Social dominance in wild and domestic Norway rats (Rattus norvegicus). Animal Behaviour. 1972;20:534-542.
Not in our library10.1016/s0003-3472(72)80018-6
- 40.
Borta A, Wöhr M, Schwarting RK. Rat ultrasonic vocalization in aversively motivated situations and the role of individual differences in anxiety-related behavior. Behavioural Brain Research. 2006;166:271-280.
Not in our library10.1016/j.bbr.2005.08.009
- 41.
Bracke MBM, Hopster H. Assessing the importance of natural behavior for animal welfare. Journal of Agricultural and Environmental Ethics. 2006;19:77-89.
Not in our library10.1007/s10806-005-4493-7
- 42.
Brenes JC, Fornaguera J. Effects of environmental enrichment and social isolation on sucrose consumption and preference: associations with depressive-like behavior and ventral striatum dopamine. Neuroscience Letters. 2008;436:278-282.
Not in our library10.1016/j.neulet.2008.03.045
- 43.
Brudzynski SM. Principles of rat communication: quantitative parameters of ultrasonic calls in rats. Behavior Genetics. 2005;35:85-92.
Not in our library10.1007/s10519-004-0858-3
- 44.
Brudzynski SM. Communication of adult rats by ultrasonic vocalization: biological, sociobiological, and neuroscience approaches. ILAR Journal. 2009;50:43-50.
Not in our library10.1093/ilar.50.1.43
- 45.
Brudzynski SM, Chiu EM. Behavioural responses of laboratory rats to playback of 22 kHz ultrasonic calls. Physiology & Behavior. 1995;57:1039-1044.
Not in our library10.1016/0031-9384(95)00003-2
- 46.
Brudzynski SM, Pniak A. Social contacts and production of 50-kHz short ultrasonic calls in adult rats. Journal of Comparative Psychology. 2002;116:73-82.
Not in our library10.1037/0735-7036.116.1.73
- 47.
Burgdorf J, Kroes RA, Moskal JR, Pfaus JG, Brudzynski SM, Panksepp J. Ultrasonic vocalizations of rats (Rattus norvegicus) during mating, play, and aggression: behavioral concomitants, relationship to reward, and self-administration of playback. Journal of Comparative Psychology. 2008;122:357-367.
Not in our library10.1037/a0012889
- 48.
Burgdorf J, Panksepp J. Tickling induces reward in adolescent rats. Physiology & Behavior. 2001;72:167-173.
Not in our library10.1016/s0031-9384(00)00411-x
- 49.
Byrne RW, Whiten A. Machiavellian Intelligence. 1988.
Not in our library
- 50.
Calhoun JB. Population density and social phatology. Scientific American. 1962;206:139-149.
Not in our library10.1038/scientificamerican0262-139
- 51.
Calhoun JB. The Ecology and Sociobiology of the Norway Rat Bethesda. 1979.
Not in our library
- 52.
Campbell DLM, Weiner SA, Starks PT, Hauber ME. Context and control: behavioural ecology experiments in the laboratory. Annales Zoologici Fennici. 2009;46:112-123.
Not in our library10.5735/086.046.0204
- 53.
- 54.
Champagne FA. Epigenetic mechanisms and the transgenerational effects of maternal care. Frontiers in Neuroendocrinology. 2008;29:386-397.
Not in our library10.1016/j.yfrne.2008.03.003
- 55.
Champagne FA, Curley JP. Epigenetic mechanisms mediating the long-term effects of maternal care on development. Neuroscience & Biobehavioral Reviews. 2009;33:593-600.
Not in our library10.1016/j.neubiorev.2007.10.009
- 56.
Chen J. Empathy for distress in humans and rodents. Neuroscience Bulletin. 2018;34:216-236.
Not in our library10.1007/s12264-017-0135-0
- 57.
Church RM. Emotional reactions of rats to the pain of others. Journal of Comparative and Physiological Psychology. 1959;52:132-134.
Not in our library10.1037/h0043531
- 58.
Clark BR, Price EO. Sexual maturation and fecundity of wild and domestic Norway rats (Rattus norvegicus). Reproduction. 1981;63:215-220.
Not in our library10.1530/jrf.0.0630215
- 59.
Cohen JE. Human population: the next half century. Science. 2003;302:1172-1175.
Not in our library10.1126/science.1088665
- 60.
Coleman RH, Ulmer FA, Doutt JK, Cook AH, Henry WH, Harriot SC, Warren ER, Miller GS, Forrest V, Goodwin GG, Bailey AM. General notes by the american society of mammalogists. Journal of Mammalogy. 1948;29:299.
Not in our library10.2307/1374666
- 61.
Colin C, Desor D. Differenciations comportementales dans des groupes de rats soumis a une difficulte d'acces a la nourriture. Behavioural Processes. 1986;13:85-100.
Not in our library10.1016/0376-6357(86)90019-7
- 62.
Cox SS, Reichel CM. Rats display empathic behavior independent of the opportunity for social interaction. Neuropsychopharmacology. 2019;76:8.
Not in our library10.1038/s41386-019-0572-8
- 63.
Daniel WJ. Cooperative problem solving in rats. Journal of Comparative Psychology. 1942;34:361-368.
Not in our library10.1037/h0062264
- 64.
Davis DE. The characteristics of rat populations. The Quarterly Review of Biology. 1953;28:373-401.
Not in our library10.1086/399860
- 65.
Dawkins MS. A user's guide to animal welfare science. Trends in Ecology & Evolution. 2006;21:77-82.
Not in our library10.1016/j.tree.2005.10.017
- 66.
de Boer SF, van der Vegt BJ, Koolhaas JM. Individual variation in aggression of feral rodent strains: a standard for the genetics of aggression and violence? Behavior Genetics. 2003;33:485-501.
Not in our library10.1023/a:1025766415159
- 67.
de Boer SF, Buwalda B, Koolhaas JM. Aggressive behavior and social stress. Concepts, Cognition, Emotion, and Behavior: Handbook of Stress. 2016.
Not in our library
- 68.
de Boer SF, Buwalda B, Koolhaas JM. Untangling the neurobiology of coping styles in rodents: towards neural mechanisms underlying individual differences in disease susceptibility. Neuroscience & Biobehavioral Reviews. 2017;74:401-422.
Not in our library10.1016/j.neubiorev.2016.07.008
- 69.
de Waal FB. Putting the altruism back into altruism: the evolution of empathy. Annual Review of Psychology. 2008;59:279-300.
Not in our library10.1146/annurev.psych.59.103006.093625
- 70.
Decety J, Bartal IB-A, Uzefovsky F, Uzefovsky F, Knafo-Noam A. Empathy as a driver of prosocial behaviour: highly conserved neurobehavioural mechanisms across species. Philosophical Transactions of the Royal Society B: Biological Sciences. 2016;371:20150077.
Not in our library10.1098/rstb.2015.0077
- 71.
Desvars-Larrive A, Baldi M, Walter T, Zink R, Walzer C. Brown rats (Rattus norvegicus) in urban ecosystems: are the constraints related to fieldwork a limit to their study? Urban Ecosystems. 2018;21:951-964.
Not in our library10.1007/s11252-018-0772-8
- 72.
Dolivo V, Taborsky M. Cooperation among Norway rats: the importance of visual cues for reciprocal cooperation, and the role of coercion. Ethology. 2015a;121:1071-1080.
Not in our library10.1111/eth.12421
- 73.
Dolivo V, Taborsky M. Norway rats reciprocate help according to the quality of help they received. Biology Letters. 2015b;11:20140959.
Not in our library10.1098/rsbl.2014.0959
- 74.
Dunbar RIM. Functional significance of social grooming in primates. Folia Primatologica. 1991;57:121-131.
Not in our library10.1159/000156574
- 75.
Duron Q, Shiels AB, Vidal E. Control of invasive rats on islands and priorities for future action. Conservation Biology. 2017;31:761-771.
Not in our library10.1111/cobi.12885
- 76.
Dusek JA, Eichenbaum H. The hippocampus and memory for orderly stimulus relations. PNAS. 1997;94:7109-7114.
Not in our library10.1073/pnas.94.13.7109
- 77.
Ebensperger LA, Sobrero R, Quirici V, Castro RA, Tolhuysen LO, Vargas F, Burger JR, Quispe R, Villavicencio CP, Vásquez RA, Hayes LD. Ecological drivers of group living in two populations of the communally rearing rodent, Octodon degus. Behavioral Ecology and Sociobiology. 2012;66:261-274.
Not in our library10.1007/s00265-011-1274-3
- 78.
Ewer RF. The biology and behaviour of a free-living population of black rats (Rattus rattus). Animal Behaviour Monographs. 1971;4:125-174.
Not in our library10.1016/s0066-1856(71)80002-x
- 79.
Feng AYT, Himsworth CG. The secret life of the city rat: a review of the ecology of urban Norway and black rats (Rattus norvegicus and Rattus rattus). Urban Ecosystems. 2014;17:149-162.
Not in our library10.1007/s11252-013-0305-4
- 80.
Fox C, Merali Z, Harrison C. Therapeutic and protective effect of environmental enrichment against psychogenic and neurogenic stress. Behavioural Brain Research. 2006;175:1-8.
Not in our library10.1016/j.bbr.2006.08.016
- 81.
Frankova M, Eliasova BK, Rodl P, Aulicky R, Frynta D, Stejskal V. Monitoring of Rattus norvegicus based on non-toxic bait containing encapsulated fluorescent dye: laboratory and semi-field validation study. Journal of Stored Products Research. 2015;64:103-108.
Not in our library10.1016/j.jspr.2015.10.002
- 82.
Galef BG. Social effects in the weaning of domestic rat pups. Journal of Comparative and Physiological Psychology. 1971;75:358-362.
Not in our library10.1037/h0030936
- 83.
Galef BG. Studies of social learning in Norway rats: a brief review. Developmental Psychobiology. 1982;15:279-295.
Not in our library10.1002/dev.420150402
- 84.
Galef BG, Mason JR, Preti G, Bean NJ. Carbon disulfide: a semiochemical mediating socially-induced diet choice in rats. Physiology & Behavior. 1988;42:119-124.
Not in our library10.1016/0031-9384(88)90285-5
- 85.
Galef BG, Marczinski CA, Murray KA, Whiskin EE. Food stealing by young Norway rats (Rattus norvegicus). Journal of Comparative Psychology. 2001;115:16-21.
Not in our library10.1037/0735-7036.115.1.16
- 86.
Galef BG. Norway rats. Current Biology. 2009;19:884-885.
Not in our library10.1016/j.cub.2009.07.031
- 87.
Galef BG, Buckley LL. Use of foraging trails by Norway rats. Animal Behaviour. 1996;51:765-771.
Not in our library
- 88.
Galef BG, Heiber L. Role of residual olfactory cues in the determination of feeding site selection and exploration patterns of domestic rats. Journal of Comparative and Physiological Psychology. 1976;90:727-739.
Not in our library10.1037/h0077243
- 89.
Galef BG, Laland KN. Social learning in animals: empirical studies and theoretical models. BioScience. 2005;55:489-499.
Not in our library10.1641/0006-3568(2005)055[0489:sliaes]2.0.co;2
- 90.
Galef BG, Sherry DF. Mother's milk: a medium for transmission of cues reflecting the flavor of mother's diet. Journal of Comparative and Physiological Psychology. 1973;83:374-378.
Not in our library10.1037/h0034665
- 91.
Galef BG, Whiskin EE. Social influences on the amount of food eaten by Norway rats. Appetite. 2000;34:327-332.
Not in our library10.1006/appe.2000.0319
- 92.
Galef BG, Whiskin EE. Socially transmitted food preferences can be used to study long-term memory in rats. Animal Learning & Behavior. 2003;31:160-164.
Not in our library10.3758/bf03195978
- 93.
Galef BG, Whiskin EE. ‘Conformity’ in Norway rats? Animal Behaviour. 2008;75:2035-2039.
Not in our library10.1016/j.anbehav.2007.11.012
- 94.
Galef BG, Wigmore SW. Transfer of information concerning distant foods: a laboratory investigation of the ‘information-centre’ hypothesis. Animal Behaviour. 1983;31:748-758.
Not in our library10.1016/s0003-3472(83)80232-2
- 95.
Gandolfi G, Parisi V. Ethological aspects of predation by rats, Rattus norvergicus (Berkenhout), on bivalves Unio pictorum L. and Cerastoderma Lamarcki (Reeve). Bolletino Di Zoologia. 1973;40:69-74.
Not in our library
- 96.
Gardner-Santana LC, Norris DE, Fornadel CM, Hinson ER, Klein SL, Glass GE. Commensal ecology, urban landscapes, and their influence on the genetic characteristics of city-dwelling Norway rats (Rattus norvegicus). Molecular Ecology. 2009;18:2766-2778.
Not in our library10.1111/j.1365-294x.2009.04232.x
- 97.
Garner JP. Stereotypies and other abnormal repetitive behaviors: potential impact on validity, reliability, and replicability of scientific outcomes. ILAR Journal. 2005;46:106-117.
Not in our library10.1093/ilar.46.2.106
- 98.
Gheusi G, Goodall G, Dantzer R. Individually distinctive odours represent individual conspecifics in rats. Animal Behaviour. 1997;53:935-944.
Not in our library10.1006/anbe.1996.0314
- 99.
Gibbs RA, Weinstock GM, Metzker ML, Muzny DM, Sodergren EJ, Scherer S, Scott G, Steffen D, Worley KC, Burch PE, Okwuonu G, Hines S, Lewis L, DeRamo C, Delgado O, Dugan-Rocha S, Miner G, Morgan M, Hawes A, Gill R, Celera, Holt RA, Adams MD, Amanatides PG, Baden-Tillson H, Barnstead M, Chin S, Evans CA, Ferriera S, Fosler C, Glodek A, Gu Z, Jennings D, Kraft CL, Nguyen T, Pfannkoch CM, Sitter C, Sutton GG, Venter JC, Woodage T, Smith D, Lee HM, Gustafson E, Cahill P, Kana A, Doucette-Stamm L, Weinstock K, Fechtel K, Weiss RB, Dunn DM, Green ED, Blakesley RW, Bouffard GG, De Jong PJ, Osoegawa K, Zhu B, Marra M, Schein J, Bosdet I, Fjell C, Jones S, Krzywinski M, Mathewson C, Siddiqui A, Wye N, McPherson J, Zhao S, Fraser CM, Shetty J, Shatsman S, Geer K, Chen Y, Abramzon S, Nierman WC, Havlak PH, Chen R, Durbin KJ, Egan A, Ren Y, Song XZ, Li B, Liu Y, Qin X, Cawley S, Worley KC, Cooney AJ, D'Souza LM, Martin K, Wu JQ, Gonzalez-Garay ML, Jackson AR, Kalafus KJ, McLeod MP, Milosavljevic A, Virk D, Volkov A, Wheeler DA, Zhang Z, Bailey JA, Eichler EE, Tuzun E, Birney E, Mongin E, Ureta-Vidal A, Woodwark C, Zdobnov E, Bork P, Suyama M, Torrents D, Alexandersson M, Trask BJ, Young JM, Huang H, Wang H, Xing H, Daniels S, Gietzen D, Schmidt J, Stevens K, Vitt U, Wingrove J, Camara F, Mar Albà M, Abril JF, Guigo R, Smit A, Dubchak I, Rubin EM, Couronne O, Poliakov A, Hübner N, Ganten D, Goesele C, Hummel O, Kreitler T, Lee YA, Monti J, Schulz H, Zimdahl H, Himmelbauer H, Lehrach H, Jacob HJ, Bromberg S, Gullings-Handley J, Jensen-Seaman MI, Kwitek AE, Lazar J, Pasko D, Tonellato PJ, Twigger S, Ponting CP, Duarte JM, Rice S, Goodstadt L, Beatson SA, Emes RD, Winter EE, Webber C, Brandt P, Nyakatura G, Adetobi M, Chiaromonte F, Elnitski L, Eswara P, Hardison RC, Hou M, Kolbe D, Makova K, Miller W, Nekrutenko A, Riemer C, Schwartz S, Taylor J, Yang S, Zhang Y, Lindpaintner K, Andrews TD, Caccamo M, Clamp M, Clarke L, Curwen V, Durbin R, Eyras E, Searle SM, Cooper GM, Batzoglou S, Brudno M, Sidow A, Stone EA, Venter JC, Payseur BA, Bourque G, López-Otín C, Puente XS, Chakrabarti K, Chatterji S, Dewey C, Pachter L, Bray N, Yap VB, Caspi A, Tesler G, Pevzner PA, Haussler D, Roskin KM, Baertsch R, Clawson H, Furey TS, Hinrichs AS, Karolchik D, Kent WJ, Rosenbloom KR, Trumbower H, Weirauch M, Cooper DN, Stenson PD, Ma B, Brent M, Arumugam M, Shteynberg D, Copley RR, Taylor MS, Riethman H, Mudunuri U, Peterson J, Guyer M, Felsenfeld A, Old S, Mockrin S, Collins F, Rat Genome Sequencing Project Consortium. Genome sequence of the Brown norway rat yields insights into mammalian evolution. Nature. 2004;428:493-521.
Not in our library10.1038/nature02426
- 100.
Girbovan C, Plamondon H. Environmental enrichment in female rodents: considerations in the effects on behavior and biochemical markers. Behavioural Brain Research. 2013;253:178-190.
Not in our library10.1016/j.bbr.2013.07.018
- 101.
Grant EC, Mackintosh JH. A comparison of the social postures of some common laboratory rodents. Behaviour. 1963;21:246-259.
Not in our library10.1163/156853963x00185
- 102.
Grasmuck V, Desor D. Behavioural differentiation of rats confronted to a complex diving-for-food situation. Behavioural Processes. 2002;58:67-77.
Not in our library10.1016/s0376-6357(01)00209-1
- 103.
Greyer MA, Markou A, Bloom F. E, Kupfer D. J. Animal models of psychiatric disorders. Psychophramacology: The Fourth Generation of Progress. 1995;787-798.
Not in our library
- 104.
Groenewoud F, Frommen JG, Josi D, Tanaka H, Jungwirth A, Taborsky M. Predation risk drives social complexity in cooperative breeders. PNAS. 2016;113:4104-4109.
Not in our library10.1073/pnas.1524178113
- 105.
Guez D, Audley C. Transitive or not: a critical appraisal of transitive inference in animals. Ethology. 2013;119:703-726.
Not in our library10.1111/eth.12124
- 106.
Hepper PG. The amniotic fluid: an important priming role in kin recognition. Animal Behaviour. 1987a;35:1343-1346.
Not in our library10.1016/s0003-3472(87)80006-4
- 107.
Hepper PG. The discrimination of different degrees of relatedness in the rat: evidence for a genetic identifier? Animal Behaviour. 1987b;35:549-554.
Not in our library10.1016/s0003-3472(87)80280-4
- 108.
Hernandez-Lallement J, van Wingerden M, Marx C, Srejic M, Kalenscher T. Rats prefer mutual rewards in a prosocial choice task. Frontiers in Neuroscience. 2014;8:443.
Not in our library10.3389/fnins.2014.00443
- 109.
Hernandez-Lallement J, van Wingerden M, Schäble S, Kalenscher T. Basolateral amygdala lesions abolish mutual reward preferences in rats. Neurobiology of Learning and Memory. 2016;127:1-9.
Not in our library10.1016/j.nlm.2015.11.004
- 110.
Hill RA, Lee PC. Predation risk as an influence on group size in cercopithecoid primates: implications for social structure. Journal of Zoology. 1998;245:447-456.
Not in our library10.1111/j.1469-7998.1998.tb00119.x
- 111.
Himmler BT, Stryjek R, Modlinska K, Derksen SM, Pisula W, Pellis SM. How domestication modulates play behavior: a comparative analysis between wild rats and a laboratory strain of Rattus norvegicus. Journal of Comparative Psychology. 2013;127:453-464.
Not in our library10.1037/a0032187
- 112.
Himmler SM, Himmler BT, Pellis VC, Pellis SM. Play, variation in play and the development of socially competent rats. Behaviour. 2016;153:1103-1137.
Not in our library10.1163/1568539x-00003307
- 113.
Himsworth CG, Feng AYT, Parsons K, Kerr T, Patrick DM. Using experiential knowledge to understand urban rat ecology: a survey of canadian pest control professionals. Urban Ecosystems. 2013a;16:341-350.
Not in our library10.1007/s11252-012-0261-4
- 114.
Himsworth CG, Parsons KL, Jardine C, Patrick DM. Rats, cities, people, and pathogens: a systematic review and narrative synthesis of literature regarding the ecology of rat-associated zoonoses in urban centers. Vector-Borne and Zoonotic Diseases. 2013b;13:349-359.
Not in our library10.1089/vbz.2012.1195
- 115.
Hofer MA. Multiple regulators of ultrasonic vocalization in the infant rat. Psychoneuroendocrinology. 1996;21:203-217.
Not in our library10.1016/0306-4530(95)00042-9
- 116.
Hopp SL, Owren MJ, Marion JR. Olfactory discrimination of individual littermates in rats (Rattus norvegicus). Journal of Comparative Psychology. 1985;99:248-251.
Not in our library10.1037/0735-7036.99.2.248
- 117.
Hurst J, Barnard CJ, Nevison CM, West CD. Housing and welfare in laboratory rats: welfare implications of isolation and social contact among caged males. Animal Welfare. 1997;6:329-347.
Not in our library
- 118.
Inglis IR, Shepherd DS, Smith P, Haynes PJ, Bull DS, Cowan DP, Whitehead D. Foraging behaviour of wild rats (Rattus norvegicus) towards new foods and bait containers. Applied Animal Behaviour Science. 1996;47:175-190.
Not in our library10.1016/0168-1591(95)00674-5
- 119.
Insel TR. From animal models to model animals. Biological Psychiatry. 2007;62:1337-1339.
Not in our library10.1016/j.biopsych.2007.10.001
- 120.
Janmaat KRL. What animals don’t do or fail to find: a novel observational approach for studying cognition in the wild. Journal of Evolutionary Anthropology. 2019;1-18.
Not in our library10.1002/evan.21794
- 121.
Johnson MTJ, Munshi-South J. Evolution of life in urban environments. Science. 2017;358:8327.
Not in our library10.1126/science.aam8327
- 122.
Kafkafi N, Agassi J, Chesler EJ, Crabbe JC, Crusio WE, Eilam D, Gerlai R, Golani I, Gomez-Marin A, Heller R, Iraqi F, Jaljuli I, Karp NA, Morgan H, Nicholson G, Pfaff DW, Richter SH, Stark PB, Stiedl O, Stodden V, Tarantino LM, Tucci V, Valdar W, Williams RW, Würbel H, Benjamini Y. Reproducibility and replicability of rodent phenotyping in preclinical studies. Neuroscience & Biobehavioral Reviews. 2018;87:218-232.
Not in our library10.1016/j.neubiorev.2018.01.003
- 123.
Keifer J, Summers CH. Putting the "Biology" back into "Neurobiology": the strength of diversity in animal model systems for neuroscience research. Frontiers in Systems Neuroscience. 2016;10:69.
Not in our library10.3389/fnsys.2016.00069
- 124.
Kiyokawa Y, Kikusui T, Takeuchi Y, Mori Y. Partner's stress status influences social buffering effects in rats. Behavioral Neuroscience. 2004;118:798-804.
Not in our library10.1037/0735-7044.118.4.798
- 125.
Kiyokawa Y, Takeuchi Y, Mori Y. Two types of social buffering differentially mitigate conditioned fear responses. European Journal of Neuroscience. 2007;26:3606-3613.
Not in our library10.1111/j.1460-9568.2007.05969.x
- 126.
Knapska E, Mikosz M, Werka T, Maren S. Social modulation of learning in rats. Learning & Memory. 2010;17:35-42.
Not in our library10.1101/lm.1670910
- 127.
Knutson B, Burgdorf J, Panksepp J. Anticipation of play elicits high-frequency ultrasonic vocalizations in young rats. Journal of Comparative Psychology. 1998;112:65-73.
Not in our library10.1037/0735-7036.112.1.65
- 128.
Koolhaas JM, de Boer SF, Buwalda B. Stress and adaptation - toward ecologically relevant animal models. Current Directions in Psychological Science. 2006;15:109-112.
Not in our library10.1111/j.0963-7214.2006.00417.x
- 129.
Koolhaas JM, Bartolomucci A, Buwalda B, de Boer SF, Flügge G, Korte SM, Meerlo P, Murison R, Olivier B, Palanza P, Richter-Levin G, Sgoifo A, Steimer T, Stiedl O, van Dijk G, Wöhr M, Fuchs E. Stress revisited: a critical evaluation of the stress concept. Neuroscience & Biobehavioral Reviews. 2011;35:1291-1301.
Not in our library10.1016/j.neubiorev.2011.02.003
- 130.
Krafft B, Colin C, Peignot P. Diving-for-food: a new model to assess social roles in a group of laboratory rats. Ethology. 1994;96:11-23.
Not in our library10.1111/j.1439-0310.1994.tb00877.x
- 131.
Lahvis GP. Unbridle biomedical research from the laboratory cage. eLife. 2017;6:e27438.
Not in our library10.7554/elife.27438
- 132.
Laland KN, Hoppitt W. Do animals have culture? Evolutionary Anthropology: Issues, News, and Reviews. 2003;12:150-159.
Not in our library10.1002/evan.10111
- 133.
Landete-Castillejos T. Chemical communication in wild Norway rats (Rattus norvegicus Berkenhout) PhD thesis. 1997.
Not in our library
- 134.
Laviola G, Hannan AJ, Macrì S, Solinas M, Jaber M. Effects of enriched environment on animal models of neurodegenerative diseases and psychiatric disorders. Neurobiology of Disease. 2008;31:159-168.
Not in our library10.1016/j.nbd.2008.05.001
- 135.
Li Z, Lu YF, Li CL, Wang Y, Sun W, He T, Chen XF, Wang XL, Chen J. Social interaction with a cagemate in pain facilitates subsequent spinal nociception via activation of the medial prefrontal cortex in rats. Pain. 2014;155:1253-1261.
Not in our library10.1016/j.pain.2014.03.019
- 136.
Li G, Wood RI. Male rats play a repeated donation game. Physiology & Behavior. 2017;174:95-103.
Not in our library10.1016/j.physbeh.2017.03.010
- 137.
Lindsey JR, Baker HJ, Suckow M, Steven H, Weisbroth C. L. F. Historical fundations. The Laboratory Rat. 2006;2-52.
Not in our library10.1016/b978-0-12-074903-4.x5000-6
- 138.
Littman RA, Lanski LM, Rhine RJ. Studies of individual and paired interactional problem solving behavior of rats (Mus norvegicus albinus). Behaviour. 1954;7:189-206.
Not in our library
- 139.
Liu D, Diorio J, Day JC, Francis DD, Meaney MJ. Maternal care, hippocampal synaptogenesis and cognitive development in rats. Nature Neuroscience. 2000;3:799-806.
Not in our library10.1038/77702
- 140.
Łopuch S, Popik P. Cooperative behavior of laboratory rats (Rattus norvegicus) in an instrumental task. Journal of Comparative Psychology. 2011;125:250-253.
Not in our library10.1037/a0021532
- 141.
MacDonald DW, Mathews F, Berdoy M, Singleton G, Lyn A, Hinds H. L, Canberra Z. Z. The behaviour and ecology of Rattus norvegicus: from opportunism to kamikaze tendencies. Ecologically-Based Management of Rodent Pests. 1999;49-80.
Not in our library
- 142.
Mackay-Sim A, Laing D. The sources of odors from stressed rats. Physiology & Behavior. 1981;27:511-513.
Not in our library10.1016/0031-9384(81)90340-1
- 143.
Marcondes FK, Bianchi FJ, Tanno AP. Determination of the estrous cycle phases of rats: some helpful considerations. Brazilian Journal of Biology. 2002;62:609-614.
Not in our library10.1590/s1519-69842002000400008
- 144.
Markman AB. Combining the strengths of naturalistic and laboratory decision-making research to create integrative theories of choice. Journal of Applied Research in Memory and Cognition. 2018;7:1-10.
Not in our library10.1016/j.jarmac.2017.11.005
- 145.
Márquez C, Rennie SM, Costa DF, Moita MA. Prosocial choice in rats depends on food-seeking behavior displayed by recipients. Current Biology. 2015;25:1736-1745.
Not in our library10.1016/j.cub.2015.05.018
- 146.
Marshall-Pescini S, Dale R, Quervel-Chaumette M, Range F. Critical issues in experimental studies of prosociality in non-human species. Animal Cognition. 2016;19:679-705.
Not in our library10.1007/s10071-016-0973-6
- 147.
Mason G, Littin KE. The humaneness of rodent pest control. Animal Welfare. 2003;12:1-37.
Not in our library
- 148.
McAuliffe K, Thornton A. The psychology of cooperation in animals: an ecological approach. Journal of Zoology. 2015;295:23-35.
Not in our library10.1111/jzo.12204
- 149.
McClintock MK, Adler NT. The role of the female during copulation in wild and domestic Norway rats (Rattus norvegicus). Behaviour. 1978;67:67-95.
Not in our library10.1163/156853978x00260
- 150.
Meerburg BG, Bonde M, Brom FWA, Endepols S, Jensen AN, Leirs H, Lodal J, Singleton GR, Pelz H-J, Rodenburg TB, Kijlstra A. Towards sustainable management of rodents in organic animal husbandry. NJAS - Wageningen Journal of Life Sciences. 2004;52:195-205.
Not in our library10.1016/s1573-5214(04)80014-9
- 151.
Meerburg BG, Brom FWA, Kijlstra A. The ethics of rodent control. Pest Management Science. 2008;64:1205-1211.
Not in our library10.1002/ps.1623
- 152.
Meerburg BG, Singleton GR, Leirs H. The year of the rat ends - time to fight hunger! Pest Management Science. 2009;65:351-352.
Not in our library10.1002/ps.1718
- 153.
Mennella JA, Blumberg MS, McClintock MK, Moltz H. Inter-litter competition and communal nursing among Norway rats: advantages of birth synchrony. Behavioral Ecology and Sociobiology. 2014;27:183-190.
Not in our library10.1007/bf00180302
- 154.
Miller LA, Fagerstone KA. Induced fertility as a wildlife management tool. Proceedings of the Vertebrate Pest Conference. 2000;19:160-168.
Not in our library10.5070/v419110055
- 155.
Mitchell D. Experiments on neophobia in wild and laboratory rats: A reevaluation. Journal of Comparative and Physiological Psychology. 1976;90:190-197.
Not in our library10.1037/h0077196
- 156.
Modlinska K, Stryjek R. Food neophobia in wild rats (Rattus norvegicus) inhabiting a changeable environment - a field study. PLOS ONE. 2016;11:e0156741.
Not in our library10.1371/journal.pone.0156741
- 157.
Mogil JS. The surprising empathic abilities of rodents. Trends in Cognitive Sciences. 2012;16:143-144.
Not in our library10.1016/j.tics.2011.12.012
- 158.
Mogil JS. Mice are people too: increasing evidence for cognitive, emotional and social capabilities in laboratory rodents. Canadian Psychology/Psychologie Canadienne. 2019;60:14-20.
Not in our library10.1037/cap0000166
- 159.
Moors PJ, Atkinson IAE, Sherley GH. Reducing the rat threat to island birds. Bird Conservation International. 1992;2:93-114.
Not in our library10.1017/s0959270900002331
- 160.
Morrison RR, Ludvigson HW. Discrimination by rats of conspecific odors of reward and nonreward. Science. 1970;167:904-905.
Not in our library10.1126/science.167.3919.904
- 161.
Mumtaz F, Khan MI, Zubair M, Dehpour AR. Neurobiology and consequences of social isolation stress in animal model - a comprehensive review. Biomedicine & Pharmacotherapy. 2018;105:1205-1222.
Not in our library10.1016/j.biopha.2018.05.086
- 162.
Munn NL. Handbook of Psychological Research on the Rat. 1950.
Not in our library
- 163.
Nakahashi W, Ohtsuki H. When is emotional contagion adaptive? Journal of Theoretical Biology. 2015;380:480-488.
Not in our library10.1016/j.jtbi.2015.06.014
- 164.
Nakashima SF, Ukezono M, Nishida H, Sudo R, Takano Y. Receiving of emotional signal of pain from conspecifics in laboratory rats. Royal Society Open Science. 2015;2:140381.
Not in our library10.1098/rsos.140381
- 165.
Oberliessen L, Hernandez-Lallement J, Schäble S, van Wingerden M, Seinstra M, Kalenscher T. Inequity aversion in rats, Rattus norvegicus. Animal Behaviour. 2016;115:157-166.
Not in our library10.1016/j.anbehav.2016.03.007
- 166.
Olsson IAS, Nevison CM, Patterson-Kane EG, Sherwin CM, Van de Weerd HA, Würbel H. Understanding behaviour: the relevance of ethological approaches in laboratory animal science. Applied Animal Behaviour Science. 2003;81:245-264.
Not in our library10.1016/s0168-1591(02)00285-x
- 167.
Palmer C, Sandøe P, Appleby M. C. Animal ethics. Animal Welfare. 2011;1-12.
Not in our library
- 168.
Panksepp J. Empathy and the laws of affect. Science. 2011;334:1358-1359.
Not in our library10.1126/science.1216480
- 169.
Parker GA. Assessment strategy and the evolution of fighting behaviour. Journal of Theoretical Biology. 1974;47:223-243.
Not in our library10.1016/0022-5193(74)90111-8
- 170.
- 171.
Parsons MH, Banks PB, Deutsch MA, Corrigan RF, Munshi-South J. Trends in urban rat ecology: a framework to define the prevailing knowledge gaps and incentives for academia, pest management professionals (PMPs) and public health agencies to participate. Journal of Urban Ecology. 2017;3:1-8.
Not in our library10.1093/jue/jux005
- 172.
Patterson-Kane EG, Hunt M, Harper D. Rats demand social contact. Animal Welfare. 2002;11:327-332.
Not in our library
- 173.
Patterson-Kane EG. Enrichment of laboratory caging for rats: a review. Animal Welfare. 2004;13:209-214.
Not in our library
- 174.
Pearson BL, Crawley JN, Eilam D, Pentkowski NS, Summers CH. Curiosity as an approach to ethoexperimental analysis: behavioral neuroscience as seen by students and colleagues of Bob Blanchard. Neuroscience & Biobehavioral Reviews. 2017;76:415-422.
Not in our library10.1016/j.neubiorev.2016.03.012
- 175.
Penn DJ, Frommen JG. Kin recognition: an overview of conceptual issues, mechanisms and evolutionary theory. Animal Behaviour - Evolution and Mechanisms. 2010.
Not in our library10.1007/978-3-642-02624-9_3
- 176.
PFMA. Pet population 2019. 2020.
Not in our library
- 177.
Philipeaux JM. Note sur l’expiration des capsules survenales chez les rats albinos (Mus rattus). Comptes Rendus Hebd Des Séances L’académie Des Sci. 1856;43:904-906.
Not in our library
- 178.
Pimentel D, Zuniga R, Morrison D. Update on the environmental and economic costs associated with alien-invasive species in the united states. Ecological Economics. 2005;52:273-288.
Not in our library10.1016/j.ecolecon.2004.10.002
- 179.
Plyusnina IZ, Solov'eva MY, Oskina IN. Effect of domestication on aggression in gray Norway rats. Behavior Genetics. 2011;41:583-592.
Not in our library10.1007/s10519-010-9429-y
- 180.
Preston SD, de Waal FB. Empathy: its ultimate and proximate bases. Behavioral and Brain Sciences. 2002;25:1-20.
Not in our library10.1017/s0140525x02000018
- 181.
Price EO. Some behavioral differences between wild and domestic Norway rats: gnawing and platform jumping. Animal Learning & Behavior. 1973;1:312-316.
Not in our library10.3758/bf03199259
- 182.
Pritchard DJ, Hurly TA, Tello-Ramos MC, Healy SD. Why study cognition in the wild (and how to test it)? Journal of the Experimental Analysis of Behavior. 2016;105:41-55.
Not in our library10.1002/jeab.195
- 183.
Prusky GT, Harker KT, Douglas RM, Whishaw IQ. Variation in visual acuity within pigmented, and between pigmented and albino rat strains. Behavioural Brain Research. 2002;136:339-348.
Not in our library10.1016/s0166-4328(02)00126-2
- 184.
Puckett EE, Park J, Combs M, Blum MJ, Bryant JE, Caccone A, Costa F, Deinum EE, Esther A, Himsworth CG, Keightley PD, Ko A, Lundkvist Åke, McElhinney LM, Morand S, Robins J, Russell J, Strand TM, Suarez O, Yon L, Munshi-South J. Global population divergence and admixture of the brown rat (Rattus norvegicus). Proceedings of the Royal Society B: Biological Sciences. 2016;283:20161762.
Not in our library10.1098/rspb.2016.1762
- 185.
Rennie SM, Moita MM, Mainen ZF. Social cognition in the rodent: nothing to be sniffed at. Trends in Cognitive Sciences. 2013;17:306-307.
Not in our library10.1016/j.tics.2013.04.011
- 186.
Rice GE, Gainer P. "Altruism" in the albino rat. Journal of Comparative and Physiological Psychology. 1962;55:123-125.
Not in our library10.1037/h0042276
- 187.
Roberts WA, Phelps MT. Transitive inference in rats: a test of the spatial coding hypothesis. Psychological Science. 1994;5:368-374.
Not in our library10.1111/j.1467-9280.1994.tb00287.x
- 188.
Rost S, Pelz HJ, Menzel S, MacNicoll AD, León V, Song KJ, Jäkel T, Oldenburg J, Müller CR. Novel mutations in the VKORC1 gene of wild rats and mice - a response to 50 years of selection pressure by warfarin? BMC Genetics. 2009;10:4.
Not in our library10.1186/1471-2156-10-4
- 189.
Russell JC, Towns DR, Anderson SH, Clout MN. Intercepting the first rat ashore. Nature. 2005;437:1107.
Not in our library10.1038/4371107a
- 190.
- 191.
Rutte C, Taborsky M. The influence of social experience on cooperative behaviour of rats (Rattus norvegicus): direct vs generalised reciprocity. Behavioral Ecology and Sociobiology. 2008;62:499-505.
Not in our library10.1007/s00265-007-0474-3
- 192.
Rutz C, Bluff LA, Weir AA, Kacelnik A. Video cameras on wild birds. Science. 2007;318:765.
Not in our library10.1126/science.1146788
- 193.
Sachs JL, Mueller UG, Wilcox TP, Bull JJ. The evolution of cooperation. The Quarterly Review of Biology. 2004;79:135-160.
Not in our library10.1086/383541
- 194.
Sales GD. The effect of 22 kHz calls and artificial 38 kHz signals on activity in rats. Behavioural Processes. 1991;24:83-93.
Not in our library10.1016/0376-6357(91)90001-g
- 195.
Sato N, Tan L, Tate K, Okada M. Rats demonstrate helping behavior toward a soaked conspecific. Animal Cognition. 2015;18:1039-1047.
Not in our library10.1007/s10071-015-0872-2
- 196.
Scheiber IBR, Weiß BM, Kingma SA, Komdeur J. The importance of the altricial - precocial spectrum for social complexity in mammals and birds - a review. Frontiers in Zoology. 2017;14:3.
Not in our library10.1186/s12983-016-0185-6
- 197.
Schmuckler MA. What is ecological validity? A dimensional analysis. Infancy. 2001;2:419-436.
Not in our library10.1207/s15327078in0204_02
- 198.
Schneeberger K, Dietz M, Taborsky M. Reciprocal cooperation between unrelated rats depends on cost to donor and benefit to recipient. BMC Evolutionary Biology. 2012;12:41.
Not in our library10.1186/1471-2148-12-41
- 199.
Schneider P, Bindila L, Schmahl C, Bohus M, Meyer-Lindenberg A, Lutz B, Spanagel R, Schneider M. Adverse social experiences in adolescent rats result in enduring effects on social competence, pain sensitivity and endocannabinoid signaling. Frontiers in Behavioral Neuroscience. 2016;10:203.
Not in our library10.3389/fnbeh.2016.00203
- 200.
Schuster R, Berger BD, Swanson HH. Cooperative social coordination and aggression: sex and strain differences in the effects of housing on gonadectomized rats with hormone replacement. Aggressive Behavior. 1988;14:179-194.
Not in our library10.1002/1098-2337(1988)14:3<179::aid-ab2480140304>3.0.co;2-9
- 201.
Schuster RH, Berger BD, Heidi H. Cooperative social coordination and aggression: II. Effects of sex and housing among three strains of intact laboratory rats differing in aggressiveness. The Quarterly Journal of Experimental Psychology. 1993;46:367-390.
Not in our library
- 202.
Schuster R. Cooperative coordination as a social behavior: experiments with an animal model. Human Nature. 2002;13:47-83.
Not in our library10.1007/s12110-002-1014-5
- 203.
Schuster R, Perelberg A. Why cooperate? an economic perspective is not enough. Behavioural Processes. 2004;66:261-277.
Not in our library10.1016/j.beproc.2004.03.008
- 204.
Schwartz LP, Silberberg A, Casey AH, Kearns DN, Slotnick B. Does a rat release a soaked conspecific due to empathy? Animal Cognition. 2017;20:299-308.
Not in our library10.1007/s10071-016-1052-8
- 205.
Schweinfurth MK, Neuenschwander J, Engqvist L, Schneeberger K, Rentsch AK, Gygax M, Taborsky M. Do female Norway rats form social bonds? Behavioral Ecology and Sociobiology. 2017a;71:98.
Not in our library10.1007/s00265-017-2324-2
- 206.
Schweinfurth MK, Stieger B, Taborsky M. Experimental evidence for reciprocity in allogrooming among wild-type Norway rats. Scientific Reports. 2017b;7:4010.
Not in our library10.1038/s41598-017-03841-3
- 207.
Schweinfurth MK, Aeschbacher J, Santi M, Taborsky M. Male Norway rats cooperate according to direct but not generalized reciprocity rules. Animal Behaviour. 2019;152:93-101.
Not in our library10.1016/j.anbehav.2019.03.015
- 208.
Schweinfurth MK, Kaufman A, Call J, Kaufman J. Reciprocity in Norway rats. The Cambridge Handbook of Animal Cognition. 2020.
Not in our library
- 209.
Schweinfurth MK, Taborsky M. No evidence for audience effects in reciprocal cooperation of Norway rats. Ethology. 2016;122:513-521.
Not in our library10.1111/eth.12499
- 210.
Schweinfurth MK, Taborsky M. The transfer of alternative tasks in reciprocal cooperation. Animal Behaviour. 2017;131:35-41.
Not in our library10.1016/j.anbehav.2017.07.007
- 211.
Schweinfurth MK, Taborsky M. Relatedness decreases and reciprocity increases cooperation in Norway rats. Proceedings of the Royal Society B: Biological Sciences. 2018a;285:20180035.
Not in our library10.1098/rspb.2018.0035
- 212.
Schweinfurth MK, Taborsky M. Norway rats (Rattus norvegicus) communicate need, which elicits donation of food. Journal of Comparative Psychology. 2018b;132:119-129.
Not in our library10.1037/com0000102
- 213.
Schweinfurth MK, Taborsky M. Reciprocal trading of different commodities in Norway rats. Current Biology. 2018c;28:594-599.
Not in our library10.1016/j.cub.2017.12.058
- 214.
Schweinfurth MK, Taborsky M. Rats play tit-for-tat instead of integrating social experience over multiple interactions. Proceedings of the Royal Society B: Biological Sciences. 2020;287:20192423.
Not in our library10.1098/rspb.2019.2423
- 215.
Setchell BP. Domestication and reproduction. Animal Reproduction Science. 1992;28:195-202.
Not in our library10.1016/0378-4320(92)90106-n
- 216.
Seyfarth RM, Cheney DL. The evolutionary origins of friendship. Annual Review of Psychology. 2012;63:153-177.
Not in our library10.1146/annurev-psych-120710-100337
- 217.
Silberberg A, Allouch C, Sandfort S, Kearns D, Karpel H, Slotnick B. Desire for social contact, not empathy, may explain "rescue" behavior in rats. Animal Cognition. 2014;17:609-618.
Not in our library10.1007/s10071-013-0692-1
- 218.
Simones PMV. Cooperation in Rats Playing an Iterated Prisoner’s Dilemma Game: Influence of a Game Matrix Formed with Qualitatively Distinct Payoffs MSc Thesis. 2007.
Not in our library
- 219.
Simpson J, Kelly JP. The impact of environmental enrichment in laboratory rats--behavioural and neurochemical aspects. Behavioural Brain Research. 2011;222:246-264.
Not in our library10.1016/j.bbr.2011.04.002
- 220.
Singleton GR, Hinds LA, Krebs CJ, Spratt DM. Rodent biology and management. Canberra. 2003.
Not in our library
- 221.
Smith JM, Harper D. Animal Signals. 2003.
Not in our library
- 222.
Sokoloff G, Blumberg MS. Competition and cooperation among huddling infant rats. Developmental Psychobiology. 2001;39:65-75.
Not in our library10.1002/dev.1030
- 223.
- 224.
Steininger F. Beiträge zur Soziologie und sonstigen Biologie der Wanderratte. Zeitschrift für Tierpsychologie. 1950;21:356-379.
Not in our library
- 225.
Stieger B, Schweinfurth MK, Taborsky M. Reciprocal allogrooming among unrelated Norway rats (Rattus norvegicus) is affected by previously received cooperative, affiliative and aggressive behaviours. Behavioral Ecology and Sociobiology. 2017;71:182.
Not in our library10.1007/s00265-017-2406-1
- 226.
Strandburg-Peshkin A, Farine DR, Couzin ID, Crofoot MC. Shared decision-making drives collective movement in wild baboons. Science. 2015;348:1358-1361.
Not in our library10.1126/science.aaa5099
- 227.
Suckow MA, Weisbroth SH, Franklin CL. The Laboratory Rat. 2006.
Not in our library
- 228.
Swanson HH, Schuster R. Cooperative social coordination and aggression in male laboratory rats: effects of housing and testosterone. Hormones and Behavior. 1987;21:310-330.
Not in our library10.1016/0018-506x(87)90017-1
- 229.
Taborsky B, Oliveira RF. Social competence: an evolutionary approach. Trends in Ecology & Evolution. 2012;27:679-688.
Not in our library10.1016/j.tree.2012.09.003
- 230.
Takahashi LK, Thomas DA, Barfield RJ. Analysis of ultrasonic vocalizations emitted by residents during aggressive encounters among rats (Rattus norvegicus). Journal of Comparative Psychology. 1983;97:207-212.
Not in our library10.1037/0735-7036.97.3.207
- 231.
Tan L, Hackenberg TD. Functional analysis of mutual behavior in laboratory rats. Journal of Comparative Psychology. 2016;130:1-11.
Not in our library10.1037/com0000015
- 232.
Telle H. Beitrag zur Erkenntnis der Verhaltensweise von Ratten, vergleichend dargestellt bei Rattus norvegicus und Rattus rattus. Zeitschrift für Angewandte Zoologie. 1966;53:129-196.
Not in our library
- 233.
Thor DH, Holloway WR. Developmental analyses of social play behavior in juvenile rats. Bulletin of the Psychonomic Society. 1984;22:587-590.
Not in our library10.3758/bf03333916
- 234.
Tibbetts EA, Dale J. Individual recognition: it is good to be different. Trends in Ecology & Evolution. 2007;22:529-537.
Not in our library10.1016/j.tree.2007.09.001
- 235.
Timmermans PJA. Social behaviour in the rat. 1978.
Not in our library
- 236.
Trezza V, Baarendse PJ, Vanderschuren LJ. The pleasures of play: pharmacological insights into social reward mechanisms. Trends in Pharmacological Sciences. 2010;31:463-469.
Not in our library10.1016/j.tips.2010.06.008
- 237.
Valenta JG, Rigby MK. Discrimination of the odor of stressed rats. Science. 1968;161:599-601.
Not in our library10.1126/science.161.3841.599
- 238.
Vasconcelos M. Transitive inference in non-human animals: an empirical and theoretical analysis. Behavioural Processes. 2008;78:313-334.
Not in our library10.1016/j.beproc.2008.02.017
- 239.
Venniro M, Zhang M, Caprioli D, Hoots JK, Golden SA, Heins C, Morales M, Epstein DH, Shaham Y. Addiction in rat models. Nature Neuroscience. 2018;21:1520-1529.
Not in our library10.1016/b978-0-12-812202-0.00002-6
- 240.
Viana DS, Gordo I, Sucena E, Moita MA. Cognitive and motivational requirements for the emergence of cooperation in a rat social game. PLOS ONE. 2010;5:e8483.
Not in our library10.1371/journal.pone.0008483
- 241.
Voelkl B, Würbel H. Reproducibility crisis: are we ignoring reaction norms? Trends in Pharmacological Sciences. 2016;37:509-510.
Not in our library10.1016/j.tips.2016.05.003
- 242.
Voznessenskaya VV, Naidenko SV, Feoktistova NY, Krivomazov GJ, Miller LA, Clark L, Singleton GR, Hinds LA, Krebs CJ, Spratt DM. Predator odours as reproductive inhibitors for Norway rats. Rats, Mice and People: Rodent Biology and Management. 2002;131-136.
Not in our library
- 243.
Weaver IC, Cervoni N, Champagne FA, D'Alessio AC, Sharma S, Seckl JR, Dymov S, Szyf M, Meaney MJ. Epigenetic programming by maternal behavior. Nature Neuroscience. 2004;7:847-854.
Not in our library10.1038/nn1276
- 244.
Webb C, Woodford P, Huchard E. Animal athics and behavioral science: an overdue discussion. Bioscience. 2019;082:778-788.
Not in our library10.1093/biosci/biz082
- 245.
Whishaw IQ, Kolb B. The Behavior of the Laboratory Rat: A Handbook with Tests. 2004.
Not in our library
- 246.
Witmer GW, Raymond-Whish S, Moulton RS, Pyzyna BR, Calloway EM, Dyer CA, Mayer LP, Hoyer PB. Compromised fertility in free feeding of wild-caught Norway rats (Rattus norvegicus) with a liquid bait containing 4-vinylcyclohexene diepoxide and triptolide. Journal of Zoo and Wildlife Medicine. 2017;48:80-90.
Not in our library10.1638/2015-0250.1
- 247.
- 248.
Wöhr M, Schwarting RKW. Ultrasonic calling during fear conditioning in the rat: no evidence for an audience effect. Animal Behaviour. 2008;76:749-760.
Not in our library10.1016/j.anbehav.2008.04.017
- 249.
Wood RI, Kim JY, Li GR. Cooperation in rats playing the iterated Prisoner's Dilemma game. Animal Behaviour. 2016;114:27-35.
Not in our library10.1016/j.anbehav.2016.01.010
- 250.
Wrighten SA, Hall CR. Support for altruistic behavior in rats. Open Journal of Social Sciences. 2016;04:93-102.
Not in our library10.4236/jss.2016.412009
- 251.
Yee JR, Cavigelli SA, Delgado B, McClintock MK. Reciprocal affiliation among adolescent rats during a mild group stressor predicts mammary tumors and lifespan. Psychosomatic Medicine. 2008;70:1050-1059.
Not in our library10.1097/psy.0b013e31818425fb
- 252.
Yorzinski JL. The cognitive basis of individual recognition. Current Opinion in Behavioral Sciences. 2017;16:53-57.
Not in our library10.1016/j.cobeha.2017.03.009
- 253.
Zentall TR. Reciprocal altruism in rats: why does it occur? Learning & Behavior. 2015;44:15-16.
Not in our library10.3758/s13420-015-0201-2
- 254.
Zhang Z. Mathematical models of wildlife management by contraception. Ecological Modelling. 2000;132:105-113.
Not in our library10.1016/s0304-3800(00)00308-2
- 255.
Zhang TY, Hellstrom IC, Bagot RC, Wen X, Diorio J, Meaney MJ. Maternal care and DNA methylation of a glutamic acid decarboxylase 1 promoter in rat Hippocampus. Journal of Neuroscience. 2010;30:13130-13137.
Not in our library10.1523/jneurosci.1039-10.2010
- 256.
Zhang YH, Zhang JX. Urine-derived key volatiles may signal genetic relatedness in male rats. Chemical Senses. 2011;36:125-135.
Not in our library10.1093/chemse/bjq103
- 257.
Ziporyn T, McClintock MK. Passing as an indicator of social dominance among female wild and domestic Norway rats. Behaviour. 1991;118:26-41.
Not in our library10.1163/156853991x00184
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