Abstract
Social network analysis in dairy calves has not been widely studied, with previous studies limited by the short study duration, and low number of animals and replicates. In this study, we investigated social proximity interactions of 79 Holstein–Friesian calves from 5 cohorts for up to 76 days. Networks were computed using 4-day aggregated associations obtained from ultrawideband location sensor technology, at 1 Hz sampling rate. The effect of age, familiarity, health, and weaning status on the social proximity networks of dairy calves was assessed. Networks were poorly correlated (non-stable) between the different 4-day periods, in the majority of them calves associated heterogeneously, and individuals assorted based on previous familiarity for the whole duration of the study. Age significantly increased association strength, social time and eigenvector centrality and significantly decreased closeness and coefficient of variation in association (CV). Sick calves had a significantly lower strength, social time, centrality and CV, and significantly higher closeness compared to the healthy calves. During and after weaning, calves had significantly lower closeness and CV, and significantly higher association strength, social time, and eigenvector centrality. These results indicate that age, familiarity, weaning, and sickness have a significant impact on the variation of social proximity interaction of calves.
Similar content being viewed by others
Introduction
Social relationships are one of the most important aspects of an animal’s life1, and can potentially shape individual differences in behaviour within a group2. Despite their relevance, social interactions, including the mechanisms, causes and consequences of individual variation in sociality, remain poorly understood3. Social behaviour in animals can be significantly impacted by several different factors with potential long-lasting effects4. For example, social conditions in early life can impact animal behaviour5, personality6, response to stress, copying behaviour7, cognitive development8 and susceptibility to disease9. Such effects can even be passed down to the next generation10.
Social network analysis (SNA) is a powerful tool11 that enables the understanding of different aspects of animal sociality, ranging from their underlying mechanistic process12 to ecological13 and evolutionary functions14. In the social network framework, nodes represent the individual animals and edges represent the relationship between pairs of individuals15,16,17. Node measures (association strength, eigenvector centrality, etc.) enable the assessment of individual social heterogeneity and help to calculate the level of connectivity of an individual15,16. Recent methodological advances in SNA16,18 and automated monitoring techniques19 have allowed researchers to investigate social interactions at high spatio-temporal resolutions20. In wild animals SNA has revealed several individual phenotypic attributes and environmental factors shaping the variability in social interactions such as age12, sex13, familiarity21, personality22 and pathogens23 among other.
SNA in farm animals overall has not been widely studied17 with only a few studies in cows20,22,24,25,26,27,28,29 and even fewer in calves30,31,32. In particular in calves, it has been shown that social networks vary according to different factors such as familiarity31, age30,33, and sex30. Results obtained in previous studies have been limited by small sample sizes, short study duration, and low number of replicates30,31,32. Regarding familiarity, Bolt et al.31 showed that calves that had been pair-housed spent more time with ex-penmates (familiar calves) once they were mixed into larger groups, but the time spent with ex-penmates decreased over time, suggesting the effect can eventually become insignificant. However, a previous study by Raussi et al.33, suggested preferences persist into adulthood, contradicting results from Bolt et al.31. This highlights the importance of longer studies to assess the impact of familiarity on social networks in calves. Age is known to impact the sociality of calves, as younger animals tend to be more in proximity to other calves33 and have lower probabilities of contact between calves with larger differences in age30. However, the impact that age has on other social measures15 (e.g. centrality), which is relevant to understand aspects such as social support, remains unknown. Additionally, results on social network stability of calves remains contradictory, with one study by Bolt et al.31 obtaining high significant stability between weeks in a 4-week study, and another study by Koene and Ipema32 finding low non-significant stability in a 10-day study. Other relevant factors in the sociality of calves, such as weaning, and health status are yet to be fully explored. Weaning is an important period in calves, as it has been shown to be a particularly stressful time34. Similarly, health is an important factor that has been shown to effect sociality in various species35,36.
The overall aim of this study was to investigate sociality in calves and its relationship with some of the most relevant factors that can affect its heterogeneity (variation in social behaviour). For this purpose, we constructed 4-day aggregated social networks from social proximity interactions of 79 calves from 5 cohorts monitored for up to 76 days. Data was collected using ultrawideband location sensor technology at 1 Hz sampling frequency, weaning stage was recorded and calves were continuously monitored and assessed for their health. The study investigated the following objectives:
-
(1)
Evaluate the stability of social proximity interactions at the group (cohort) level during the period of the study and investigate if calves associate heterogeneously in each of the social proximity networks for all the cohorts.
-
(2)
Investigate if social associations are affected by difference in age, familiarity, and differences in health status.
-
(3)
Examine the effect of factors such as age, stage of weaning and health status on social measures at the node level (strength, social time, closeness, centrality and coefficient of variation in association strength).
Materials and methods
The present study was reviewed and approved by the Ethical Committee at the School of Veterinary Medicine and Science, University of Nottingham (Approval Number 1481 150603). All experiments were performed in accordance with relevant guidelines and regulations of the School of Veterinary Medicine and Science, University of Nottingham.
Data collection and processing
Animals, housing and farm management
The study took place at the Centre for Dairy Science Innovation at the University of Nottingham, UK, between 14th of May 2021 and 26th of November 2021. In total 79 calves from 5 different cohorts of 15 to 16 calves each were included in the study, as described in Table 1. All calves were female (F), Holstein Friesian (HF). At birth, animals were kept in pairs as per normal farm management until the calves were at least 2 weeks of age and a cohort was formed with a minimum of 15 calves. Each cohort of calves was moved to one of two adjacent straw-bedded pens as illustrated in Fig. 1. Each rectangular pen measured 6 m × 10 m, had an automatic feeder, a tank with concentrates and water trough. The feeder zone in Fig. 1 represented an area of 1.5 m × 3 m around the automatic feeder. Calves had access to concentrates and water ad-libitum. Ethical permission for all the observational procedures was obtained for the School of Veterinary Medicine and Science, University of Nottingham (unique reference number 1481 150603).
Weaning and health monitoring
In this study all calves were fed milk replacer (Milkivit Energizer ECM, Trouw Nutrition GB) from an automatic feeder for the entire milk-feeding period. During the study calves were equipped with RFID ear tags that enabled their identity to be recognised by the feeding station. The automatic feeder distributed a maximum of 2 L every 2 h, up to a total daily allowance of 10 L daily for the first 35 days. From day 36 the allowance was reduced by 400 ml/day until reduced to zero on day 60. Besides their daily milk allowance, calves had also ad libitum access to concentrates (FiMLAC Sweet Start Pellets), chopped straw and water.
Health monitoring and sick definition
Calves were health monitored for bovine respiratory diseases (BRD), by an experienced veterinary surgeon who manually inspected all calves twice a week for signs of ill health using a modified version of the Wisconsin-Madison calf health scoring system37. This health assessment included clinical examination of nasal discharge, ear score, eye score and rectal temperature score. Each of these categories ranged from 0 to 3, where 0 = normal, 1 = mildly abnormal, 2 = moderately abnormal, and 3 = severely abnormal. The total health score was the sum of all the different individual scores. As per the recommendations of the scoring system37, calves with a total score from 0 to 2 considered were considered as being normal (healthy), scores 3 and 4 considered as moderate and values of more or equal to 5 as being sick. Bovine respiratory disease is the most common cause of sickness in pre-weaned calves38. There was no evidence of any other infections as per clinical exam. When assessed for health, animals showing signs of ill health were treated according to farm protocols. All calves in the study were vaccinated at 9 days of age with a respiratory vaccine (Rispoval RS + Pi3 IntraNasal; Zoetis).
Location position system
The location data was collected using collar mounted sensors fitted to each calf. The collars had a counterweight to help maintain the position of the sensors and were fitted 2 to 3 weeks before the calves were moved into the trial pens to allow time for habituation.
Each individual indoor tracking sensor (Sewio Leonardo iMU tags) provided relative local coordinates in (x,y) using ultrawideband sensor technology39 at a range of different frequencies. For this study, location data was collected continuously over the duration of each cohort using a sampling frequency of 1 Hz. Local position within this system was computed using distance triangulation from 4 fixed anchors located at the corners of the two adjacent pens as shown in Fig. 1.
A validation test on the accuracy of the location data was performed before the start of the study using 20 sensors at 9 static positions in the pen in a similar manner to40. The mean circular error probability (CEP) and a measure of the accuracy (DIST) were computed on the validation test. The CEP represents the precision of the location, and it is calculated as the radius of the circle, centred at the mean location, with 50% of the points lying within it. DIST represents the mean distance between the known ground truth location and the location obtained by the sensor. In the validation trial, the mean circular error probability (CEP) was 0.15 m (range 0.12–0.28 m) and DIST was found to be 0.17 m (range 0.13–0.33 m).
Pre-processing and cleaning of positional data
The location data from the 1st day when calves were moved into the pens were removed. Additionally, times when there were human visits to the pen were removed since the proximity of the calves might have been affected at these times. Times when sensors were replaced due to battery failure were also removed from the dataset as well as times when location coordinates were placed outside of the pens due to location error. In total 1.55% (5 days of the 323 total) of the data was removed from the 5 cohorts. Additionally, sensor location data was smoothed using a simple moving average over a 10-s window to improve accuracy.
Determining proximity interactions and social network construction
Social interactions between animals were defined as proximity interactions below a threshold distance for a minimum duration of time between a pair of calves (dyads). Such proximity interactions were non-directed (calf A being close to calf B results in calf B being close to calf A). The selection of both space and temporal thresholds was based on observations of biologically meaningful social interactions as well as the minimum distance between calves due to their size. In this study, we used a distance of 1 m and duration of 3 min for the spatial and temporal thresholds, respectively. We tested a range of different thresholds for both space (0.8 and 1.2 m) and time (2 and 4 min) and qualitatively similar results were obtained. Pair wise proximity interactions were utilised to compute edge weights (association) between individual nodes (calves). The following association index: (\({{{E}}}_{{{A}}{{B}}}=\frac{{{X}}}{{{X}}+{{{Y}}}_{{{A}}{{B}}}+{{{Y}}}_{{{A}}}+{{{Y}}}_{{{B}}}}\)) was utilised to compute the edge weights between any pair of individuals when the data had missing observations (represented by missing location) as suggested in16,18. In the association index, X represents the number of interactions where both animals co-occurred, YA and YB represent the number of samples where only animal A and B, were seen respectively, and YAB is the number of times both animals were observed but not in close proximity. Non-directed, weighted association matrices representing the social proximity networks, were obtained for consecutive 4-day periods of data using association indices as described before. The selection of 4-day periods was done in order to align with the health monitoring information.
Analysis
Non-directed weighted matrices for each 4-day period for all cohorts were converted into network graphs using the package “igraph” in R41 to produce visualisations. In Fig. 2 we show the social network for each individual period for cohort 4. The visualisation was produced using Fruchterman–Reingold algorithm on filter networks, were edges with less than the mean were omitted.
Network stability (temporal variation in sociality)
Temporal variation in sociality was assessed for each cohort using all the different adjacent matrices previously obtained from association indices (edge weights) over all 4-day aggregated periods. Across all cohorts, each 4-day association matrix was compared to each other using the mantel test from the package “vegan” in R41 to determine the level of correlation between any two different 4-day periods. The Mantel test provided the significance of the correlation using a quadratic assignment procedure for node permutation with n = 10,000 for all the tests.
Social differentiation
We tested if the associations between calves were more heterogeneous (have higher variation) than what would be expected given the null hypothesis that they associated uniformly. For this test we used the coefficient of variation in association (edge weight) for social differentiation as computed in Withehead18, as the standard error over the mean where the standard error was estimated \(SE= \alpha \sqrt{\frac{1-\alpha }{x}}\) where \(\alpha \) is the calculated associated index and x is the number of samples in which A and B were interacting (proximity interaction). The original test statistic (observed coefficient of variation in association) was compared to the test statistic obtained by randomly permuting the nodes of the observed network and calculating the proportion of times when the test statistic from the permutations was equal to or more than the original test statistic. This test was performed for each individual 4-day aggregated proximity-based network on all the different cohorts using 10,000 permutations.
Assortment by age, health status and familiarity
Assortment measures the tendency of individuals with the same phenotypic characteristics to associate more than what would be expected if they were associating uniformly15,16,18. For example, older calves might interact more with other calves of similar age than with younger calves. Assortment is considered a group measure in social network analysis15,16,18. To test if calves associated more or less with calves of different ages, different health status, or calves they were more familiar with, we tested for assortment for each of these variables. Assortment testing was performed during the whole duration of the study on all the different 4-day periods ranging from 1 to 19 depending on how long each cohort was monitored. Familiarity was measured as the number of days they were in contact before moved into the trial pens and ranged between 0 to 51 days. The difference in age was computed between any pair of individuals as the number of days between the birth dates of the two, whereas the difference in health was computed using differences in health status with categories 0, 1 and 2, representing healthy, moderate, and sick, respectively. A MCMCglmm framework42 with the association index (edge weight) between any pair of individuals (IDi, IDj) as an output and fixed factors (difference in age, difference in health, and familiarity), was utilised to investigate assortment. Within this framework cohort, \({ID}_{i}\) and \({ID}_{j}\) were included as random variables. The inclusion of node IDs allowed to account for multiple membership of the association as suggested by Franks et al.43. Edge weight (association index) was log transformed to satisfy the assumptions of normality. Similarly, the model was also assessed for heteroscedasticity by assessing residual vs fitted values. Independence was dealt using the multiple membership random effect as described in Franks43.
Impact of age, calf health and weaning on sociality measures
We investigated the impact that weaning and health have on sociality by fitting a mixed effect linear model using the lme4 package44 in R41 for each of the following social measures: total social time, association strength, eigenvector centrality, closeness, and coefficient of variation in association strength.
Total social time was computed as the sum of the proximity interactions for each individual calf with the rest of the group. To convert this value into minutes it was then multiplied by 3 given that proximity interactions were calculated using a 3-min threshold. This measure was computed without using association index. The rest of the social measures (association strength, eigenvector centrality, closeness, and coefficient of variation in association) were computed using the association index from pair wise proximity interactions at each individual 4-day period as follows:
Association strength was computed as the sum of the edge weights (association indices) for each individual calf, and it represents individuals’ sociality or social activity15,16.
Eigenvector centrality is the sum of the centralities of an individuals’ neighbours, and it is computed as the first non-negative value obtained from the adjacency matrix representation of the network. Eigenvector centrality represents the “importance” of the individual within the network15,16.
Closeness centrality is measured in terms of shortest paths between the node with all the rest of the nodes in the network and it represents its potential for disease or information transmission45.
Coefficient of variation in association is a standardised, unit free measure of dispersion which was computed as suggested by Whitehead and indicates the level of heterogeneity in associations18.
The models were defined as follows:
where Y represents each of the social measures (total social time, association strength, eigenvector centrality, closeness and coefficient of variation in association), X represents the fixed effects for the 4-day observational time unit: age of the calf (taken at the end of the 4-day period), weaning stage and health status of the calf, respectively. Z represents the random effects: Calf ID and period nested within cohort and \(\varepsilon \) represents the residuals. Weaning was defined as categorical variable with three categories (non- weaned, step-down, and weaned). Health was defined as categorical variable with three categories (healthy, moderate, and sick) as previously defined. For each of the models (e.g., association strength), the outcome variable and fixed factors were obtained per individual calf. The Benjamini–Hochberg (BH) procedure46 was applied for multiple significant testing over the same data.
Ethics
Ethical permission for all the methods of the observational trial described was obtained for the School of Veterinary Medicine and Science, University of Nottingham (unique reference number 1481 150603). All methods are reported in accordance with the ARRIVE guidelines47.
Results
Temporal variation in sociality
Out of all the correlations between the different periods, 41.09% were significant. Figure 3 shows the distribution of the significant correlation values between different periods as well as boxplot with the significant correlation between different periods grouped by the difference in time period (e.g. a difference of 2 can come from periods 2 and 4, 3 and 5, etc.). The significant correlations had a mean of 0.3423 (± 0.0984).
Social differentiation
For all cohorts there was a significant social differentiation at each 4-day aggregated proximity-based network, with the exception of period 5 for cohort 1. The results of the social differentiation test are shown in the Supplementary Material (Table 1). This demonstrates that calves in general calves associated heterogeneously, expending more time with certain individuals than with others.
Assortment by age, health status and familiarity
There was significant assortment by familiarity in all periods for all cohorts, as calves spent significantly more time with other calves that they were familiar with. There was also significant assortment by difference in age in weeks 1–2, 4–12 and 16–19, meaning that calves spent less time with calves of different ages (see Supplementary Material, Table 2). There was also significant assortment by difference in health only at period 1, indicating that calves spent less time with those with a different health status only in the first 4-day period.
Association between age, individual health/weaning and sociality measures
The results from the linear mixed model showed that older calves had significantly lower association strength (t = − 6.065, p-value = 0.0024), significantly lower social time (t = − 4.331, p-value = 0.0031), significantly higher closeness (t = 6.85, p-value = 0.0007) and lower centrality (t = − 5.866, p-value = 0.0001) than younger calves (Table 2).
Sick calves had significantly higher closeness (t = 3.81, p-value = 0.0004) and significantly lower (t = − 3.17, p-value = 0.0031) association strength, social time (t = − 2.42, p-value = 0.0200), centrality (t = − 2.95, p-value = 0.0054) and coefficient of variation (t = − 2.86, p-value = 0.0061), than healthy calves.
During the step-down weaning process calves had significantly higher strength (t = 5.38 p-value = 0.0024), social time (t = 6.58, p-value = 0.0001) and centrality (t = 3.75, p-value 0.0335), and significantly lower closeness (t = − 5.44, p-value = 0.0002)and coefficient of variation (t = − 3.38, p-value = 0.0061) than pre-weaned calves. Similarly, weaned calves had significantly higher strength (t = 3.16 p-value = 0.0061), social time (t = 3.75, p-value = 0.002) and centrality (t = 4.86, p-value 0.0035), and significantly lower closeness (t = − 4.02, p-value = 0.0012), and coefficient of variation (t = − 2.78, p-value = 0.01) than calves before weaning.
Discussion
This is the first study that investigated social networks and social proximity interactions obtained from high temporal resolution of location data in calves, and the impact of the most relevant factors on calves’ sociality. We obtained novel insights on the effect that age, weaning stage and health status have on several social metrics at the node level. We evaluated the stability of social proximity interactions and the social differentiation and investigated for the first time the effect that familiarity, difference in health and difference in age have on associated social network strength.
To the author’s knowledge, this is the first study that shows a significant effect of weaning stage and health status on social measures at the individual animal level. While previous studies have shown an increase in the number of vocalisations during and after weaning31, no information on social proximity encounters and social network metrics has been previously reported. Our results show that during weaning calves had higher association strength, social time and centrality, and lower closeness and coefficient of variation than pre-weaned calves. This means that during the weaning period calves were socialising more (higher number of interactions and association strength) and were more central than non-weaned calves while they were less close to other calves and had lower heterogeneity in their interactions (lower coefficient of variation in association). For example, during weaning calves had approximately 180.74 more proximity encounters of three-minute duration (Table 2), which correspond to an additional 9.03 h socialising. Weaning is known to be a stressful time for animals34,48,49 and calves might alleviate the stress via ‘social support’ as this has been shown to improve individuals’ abilities to cope with challenges50. In older cattle, it has been shown that after being exposed to a stressor event (post-handling) animals will prefer social environments that allow social interactions with peers51. Eigenvector centrality can be interpreted as the social support or social capital of an individual15 and hence higher centrality indicates higher support during this stressful time. Additionally, it has been previously shown that calves going through a painful procedure such as disbudding spend more time with other calves recovering from the procedure52. Once the calves were weaned, they continued to have higher association strength, social time, eigenvector centrality and lower closeness and coefficient of variation in association in our study. This might be due to the fact that weaned calves spend less time around the feeder which might allow them to spend more time socialising and thus increases their association strength, social time and their position within the network (eigenvector centrality).
Another key result of this study was the impact of health status on sociality in calves. Previous studies have only investigated if there were any significant differences in health status between different housing types31, with no information on the effect that sickness has on social measures. We showed that sick calves had lower association strength, social time, eigenvector centrality, and coefficient of variation in association and higher closeness. A lower coefficient of variation in association indicates that calves increase the number of non-preferential proximity encounters. Eigenvector centrality represent the importance of the animal within the group16 and as such it might require high levels of energy to maintain. Sick calves affected by bovine respiratory disease (BRD) have lower feed consumption53 (energy intakes), hence by reducing their eigenvector centrality animals might be adopting a strategy to maintain their energy balance during periods of illness54. Lower association strength and eigenvector centrality during sickness have been shown in other species36. Closeness has been used as measure of disease transmission15,16,45 indicating that nodes with higher values will transmit more easily diseases within the group. Changes in social behaviour might be the result of parasites manipulating the individual behaviour of the host to facilitate parasite transmission55,56. In our study, undirected networks were obtained from proximity interactions, and hence it was not possible to determine if sick animals actively avoided social interactions with others, or if other healthy animals avoided the sick animal or a combination of both.
Our results showed that older calves associated less than younger individuals (lower strength and social time), which is in agreement with a previous study33. This might be due to higher social exploration57 in younger calves while older calves become more solitary as they age, which has been shown in other species (i.e. giraffes57,58). Additionally, older calves had lower centrality (social rank), higher closeness, and higher coefficient of variation. This might be the result of animals strengthening their proximity interactions with specific individuals over time. Additionally, our results showed assortment by age difference in most of the different periods, indicating that calves associated more with others of similar age.
Our results show that assortment by familiarity was maintained through the whole duration of this study (up to the 19th period, which corresponds to 76 days), supporting previous evidence of early social relationships maintained over long periods of time33,59. Although this result is in agreement with previous research showing that early preferences persist for longer durations of times up to adulthood33, it is in contrast with Bolt et al.31 who found that familiarity reduced overtime. The differences in the results might be due to the duration of time investigated (4 weeks in31), as well as the duration of time that calves were paired before being grouped.
In the current study calves associated heterogeneously for the majority of the 4-day periods, meaning that they had more interactions with certain individuals, which is in agreement with previous studies also showing heterogeneity in social networks in dairy calves20,31. A higher degree of selectivity has been previously linked to pessimism in dairy calves60, and therefore highlights the possible link between social network measures and personality measures, for which there is emerging evidence in calves61,62,63. Additionally, the results on network stability indicate that networks were not stable all the time as only 41% of all the possible correlations between any two 4-day aggregated networks were significantly positive. When significantly correlated, all values were positive and relatively high (r = 0.3423 (± 0.0984)), and this did not depend on the time difference between the two different periods (e.g., longer the time between periods larger the correlation or vice versa). Previous studies have reported contradicting results for network stability with20,26,32 who also reported no temporal stability in cattle and calf networks and Bolt et al.31 who showed high significant correlation between all weeks in calves. Disparity between our results and those from Bolt et al.31 might be due to the differences in the methodology, as they have a larger group size (n = 40) in a larger pen (200 m2) and the differences in the preceding rearing and grouping protocols. Additionally, it has been shown that stability in social proximity patterns might depend on the activity that calves are performing when in proximity (lying and standing)60. Hence, network stability results obtained in this study might be different if social proximity networks were to be separated by activity, which could be explored in future work.
Our results indicate that age, familiarity, weaning and sickness have a significant importance in the variation of social proximity interaction of calves. However, other important factors such as differences in animal personality within a group can also drive collective behaviour and hence sociality in animals1,64. Variation in sociality can also play a role in animal personality, creating a feedback loop1. Future work could focus on understanding the dynamics between animal personality and sociality in calves. Moreover, sociality can also be investigated as a personality trait by quantifying the consistency of an individual’s network position over time and contexts1,16. One limitation of the current study is that only one type of interaction has been investigated: social proximity interactions, which are a type of affiliative interaction, without examining other affiliative (e.g., allogrooming) or agnostic interactions (e.g. displacements). It has been shown that the effect of illness on social interactions depends on the type behaviour65 and hence other types of interactions might display different effects. Future research should include such social behaviours which can be potentially monitored using a combination of technologies to detect and quantify them24.
Despite some of the limitations of the current study, our results provide new insights into the social behaviour of calves and the factors that have a significant impact on it, and hence it has potential for use on developing stress-buffering (coping) strategies for the improvement of the welfare of farm animals50. Some of the key strengths of this study are the use of multiple replicates (5 replicates), the long-term monitoring (up to 76 days) and the large total number of animals (76 calves) compared to previous studies30,31,32. The number of replicates has been shown to be highly important for hypothesis testing in social behaviour66. Moreover, the novel insights on the factors that affect and/or shape social interactions in calves can be used to develop and implement better farm practices67 and could lead to the development of algorithms for the automatic detection of sick animals, which would ultimately improve farm animal health and welfare.
Data availability
The datasets supporting the results of this article are available upon reasonable request from the corresponding author (Jorge.VazquezDiosdado@nottingham.ac.uk).
References
Gartland, L. A., Firth, J. A., Laskowski, K. L., Jeanson, R. & Ioannou, C. C. Sociability as a personality trait in animals: Methods, causes and consequences. Biol. Rev. https://doi.org/10.1111/brv.12823 (2021).
Bergmüller, R. & Taborsky, M. Adaptive behavioural syndromes due to strategic niche specialization. BMC Ecol. 7, 12. https://doi.org/10.1186/1472-6785-7-12 (2007).
Massen, J. J. M., Sterck, E. H. M. & de Vos, H. Close social associations in animals and humans: Functions and mechanisms of friendship. Behaviour 147, 1379–1412. https://doi.org/10.1163/000579510X528224 (2010).
Haller, J., Harold, G., Sandi, C. & Neumann, I. D. Effects of adverse early-life events on aggression and anti-social behaviours in animals and humans. J. Neuroendocrinol. 26, 724–738. https://doi.org/10.1111/jne.12182 (2014).
Carlson Bruce, A. Early life experiences have complex and long-lasting effects on behavior. Proc. Natl. Acad. Sci. 114, 11571–11573. https://doi.org/10.1073/pnas.1716037114 (2017).
Zablocki-Thomas, P. B. et al. Personality and performance are affected by age and early life parameters in a small primate. Ecol. Evol. 8, 4598–4605. https://doi.org/10.1002/ece3.3833 (2018).
Langenhof, M. R. & Komdeur, J. Why and how the early-life environment affects development of coping behaviours. Behav. Ecol. Sociobiol. 72, 34–34. https://doi.org/10.1007/s00265-018-2452-3 (2018).
Daros, R. R., Costa, J. H. C., von Keyserlingk, M. A. G., Hötzel, M. J. & Weary, D. M. Separation from the dam causes negative judgement bias in dairy calves. PLoS One 9, e98429. https://doi.org/10.1371/journal.pone.0098429 (2014).
Grześkowiak, ŁM. et al. Impact of early-life events on the susceptibility to Clostridium difficile colonisation and infection in the offspring of the pig. Gut Microbes 10, 251–259. https://doi.org/10.1080/19490976.2018.1518554 (2019).
Schmauss, C., Lee-McDermott, Z. & Medina, L. R. Trans-generational effects of early life stress: The role of maternal behavior. Sci. Rep. 4, 4873. https://doi.org/10.1038/srep04873 (2014).
Brask, J. B., Ellis, S. & Croft, D. P. Animal social networks: An introduction for complex systems scientists. J. Complex Netw. 9, cnab001. https://doi.org/10.1093/comnet/cnab001 (2021).
Almeling, L., Hammerschmidt, K., Sennhenn-Reulen, H., Freund, A. M. & Fischer, J. Motivational shifts in aging monkeys and the origins of social selectivity. Curr. Biol. 26, 1744–1749. https://doi.org/10.1016/j.cub.2016.04.066 (2016).
Borgeaud, C., Sosa, S., Sueur, C. & Bshary, R. The influence of demographic variation on social network stability in wild vervet monkeys. Anim. Behav. 134, 155–165. https://doi.org/10.1016/j.anbehav.2017.09.028 (2017).
Cantor, M. et al. The importance of individual-to-society feedbacks in animal ecology and evolution. J. Anim. Ecol. 90, 27–44. https://doi.org/10.1111/1365-2656.13336 (2021).
Sosa, S., Sueur, C. & Puga-Gonzalez, I. Network measures in animal social network analysis: Their strengths, limits, interpretations and uses. Methods Ecol. Evol. 12, 10–21. https://doi.org/10.1111/2041-210X.13366 (2021).
Farine, D. R. & Whitehead, H. Constructing, conducting and interpreting animal social network analysis. J. Anim. Ecol. 84, 1144–1163. https://doi.org/10.1111/1365-2656.12418 (2015).
Neethirajan, S. & Kemp, B. Social network analysis in farm animals: Sensor-based approaches. Animals 11, 434. https://doi.org/10.3390/ani11020434 (2021).
Whitehead, H. Analyzing Animal Societies. University of Chicago Press, Chicago, IL, USA (2008).
Smith, J. E. & Pinter-Wollman, N. Observing the unwatchable: Integrating automated sensing, naturalistic observations and animal social network analysis in the age of big data. J. Anim. Ecol. 90, 62–75. https://doi.org/10.1111/1365-2656.13362 (2021).
Chen, S., Ilany, A., White, B. J., Sanderson, M. W. & Lanzas, C. Spatial-temporal dynamics of high-resolution animal networks: What can we learn from domestic animals?. PLoS One 10, e0129253. https://doi.org/10.1371/journal.pone.0129253 (2015).
Atton, N., Galef, B. J., Hoppitt, W., Webster, M. M. & Laland, K. N. Familiarity affects social network structure and discovery of prey patch locations in foraging stickleback shoals. Proc. R. Soc. B Biol. Sci. 281, 20140579. https://doi.org/10.1098/rspb.2014.0579 (2014).
Ilany, A. & Akçay, E. Personality and social networks: A generative model approach. Integr. Comp. Biol. 56, 1197–1205. https://doi.org/10.1093/icb/icw068 (2016).
Romano, V. et al. Modeling infection transmission in primate networks to predict centrality-based risk. Am. J. Primatol. 78, 767–779. https://doi.org/10.1002/ajp.22542 (2016).
Ren, K., Bernes, G., Hetta, M. & Karlsson, J. Tracking and analysing social interactions in dairy cattle with real-time locating system and machine learning. J. Syst. Archit. 116, 102139. https://doi.org/10.1016/j.sysarc.2021.102139 (2021).
Boyland, N. K., Mlynski, D. T., James, R., Brent, L. J. N. & Croft, D. P. The social network structure of a dynamic group of dairy cows: From individual to group level patterns. Appl. Anim. Behav. Sci. 174, 1–10. https://doi.org/10.1016/j.applanim.2015.11.016 (2016).
Chopra, K. et al. Proximity interactions in a permanently housed dairy herd: Network structure, consistency, and individual differences. Front. Vet. Sci. 7, 583715 (2020).
Šárová, R. et al. Pay respect to the elders: Age, more than body mass, determines dominance in female beef cattle. Anim. Behav. 86, 1315–1323. https://doi.org/10.1016/j.anbehav.2013.10.002 (2013).
Foris, B., Haas, H. G., Langbein, J. & Melzer, N. Familiarity influences social networks in dairy cows after regrouping. J. Dairy Sci. 104, 3485–3494. https://doi.org/10.3168/jds.2020-18896 (2021).
Foris, B., Zebunke, M., Langbein, J. & Melzer, N. Comprehensive analysis of affiliative and agonistic social networks in lactating dairy cattle groups. Appl. Anim. Behav. Sci. 210, 60–67. https://doi.org/10.1016/j.applanim.2018.10.016 (2019).
de Freslon, I., Martínez-López, B., Belkhiria, J., Strappini, A. & Monti, G. Use of social network analysis to improve the understanding of social behaviour in dairy cattle and its impact on disease transmission. Appl. Anim. Behav. Sci. 213, 47–54. https://doi.org/10.1016/j.applanim.2019.01.006 (2019).
Bolt, S. L., Boyland, N. K., Mlynski, D. T., James, R. & Croft, D. P. Pair housing of dairy calves and age at pairing: Effects on weaning stress, health production and social networks. PLoS One 12, e0166926. https://doi.org/10.1371/journal.pone.0166926 (2017).
Koene, P. & Ipema, B. Social networks and welfare in future animal management. Animals (Basel) 4, 93–118. https://doi.org/10.3390/ani4010093 (2014).
Raussi, S. et al. The formation of preferential relationships at early age in cattle. Behav. Proc. 84, 726–731. https://doi.org/10.1016/j.beproc.2010.05.005 (2010).
Weary, D. M., Jasper, J. & Hötzel, M. J. Understanding weaning distress. Appl. Anim. Behav. Sci. 110, 24–41. https://doi.org/10.1016/j.applanim.2007.03.025 (2008).
Lopes, P. C., Block, P. & König, B. Infection-induced behavioural changes reduce connectivity and the potential for disease spread in wild mice contact networks. Sci. Rep. 6, 31790. https://doi.org/10.1038/srep31790 (2016).
Ripperger, S. P., Stockmaier, S. & Carter, G. G. Tracking sickness effects on social encounters via continuous proximity sensing in wild vampire bats. Behav. Ecol. 31, 1296–1302. https://doi.org/10.1093/beheco/araa111 (2020).
McGuirk, S. M. & Peek, S. F. Timely diagnosis of dairy calf respiratory disease using a standardized scoring system. Anim. Health Res. Rev. 15, 145–147. https://doi.org/10.1017/s1466252314000267 (2014).
Callan, R. J. & Garry, F. B. Biosecurity and bovine respiratory disease. Vet. Clin. N. Am. Food Anim. Pract. 18, 57–77. https://doi.org/10.1016/S0749-0720(02)00004-X (2002).
Sewio. Tag Leonardo iMU/Personal. https://docs.sewio.net/docs/tag-leonardo-imu-personal-30146967.html (2022).
Barker, Z. E. et al. Use of novel sensors combining local positioning and acceleration to measure feeding behavior differences associated with lameness in dairy cattle. J. Dairy Sci. 101, 6310–6321. https://doi.org/10.3168/jds.2016-12172 (2018).
Team, R. C. R: A Language and Environment for Statistical Computing.
Hadfield, J. D. MCMC methods for multi-response generalized linear mixed models: The MCMCglmm R package. J. Stat. Softw. 33, 1–22. https://doi.org/10.18637/jss.v033.i02 (2010).
Franks, D. W., Weiss, M. N., Silk, M. J., Perryman, R. J. Y. & Croft, D. P. Calculating effect sizes in animal social network analysis. Methods Ecol. Evol. 12, 33–41. https://doi.org/10.1111/2041-210X.13429 (2021).
Bates, D., Mächler, M., Bolker, B. & Walker, S. Fitting linear mixed-effects models using lme4. J. Stat. Softw. 67, 1–48. https://doi.org/10.18637/jss.v067.i01 (2015).
Bell, D. C., Atkinson, J. S. & Carlson, J. W. Centrality measures for disease transmission networks. Soc. Netw. 21, 1–21. https://doi.org/10.1016/S0378-8733(98)00010-0 (1999).
Benjamini, Y. & Hochberg, Y. Controlling the false discovery rate: A practical and powerful approach to multiple testing. J. R. Stat. Soc. Ser. B (Methodol.) 57, 289–300. https://doi.org/10.1111/j.2517-6161.1995.tb02031.x (1995).
PercieduSert, N. et al. Reporting animal research: Explanation and elaboration for the ARRIVE guidelines 2.0. PLoS Biol. 18, e3000411. https://doi.org/10.1371/journal.pbio.3000411 (2020).
Hulbert, L. E. & Moisá, S. J. Stress, immunity, and the management of calves. J. Dairy Sci. 99, 3199–3216. https://doi.org/10.3168/jds.2015-10198 (2016).
Sweeney, B. C., Rushen, J., Weary, D. M. & de Passillé, A. M. Duration of weaning, starter intake, and weight gain of dairy calves fed large amounts of milk. J. Dairy Sci. 93, 148–152. https://doi.org/10.3168/jds.2009-2427 (2010).
Rault, J.-L. Friends with benefits: Social support and its relevance for farm animal welfare. Appl. Anim. Behav. Sci. 136, 1–14. https://doi.org/10.1016/j.applanim.2011.10.002 (2012).
Ishiwata, T., Kilgour, R. J., Uetake, K., Eguchi, Y. & Tanaka, T. Choice of attractive conditions by beef cattle in a Y-maze just after release from restraint. J. Anim. Sci. 85, 1080–1085. https://doi.org/10.2527/jas.2006-405 (2007).
Ede, T., von Keyserlingk, M. A. G. & Weary, D. M. Social approach and place aversion in relation to conspecific pain in dairy calves. PLoS One 15, e0232897. https://doi.org/10.1371/journal.pone.0232897 (2020).
Cantor, M. C., Renaud, D. L., Neave, H. W. & Costa, J. H. C. Feeding behavior and activity levels are associated with recovery status in dairy calves treated with antimicrobials for Bovine Respiratory Disease. Sci. Rep. 12, 4854. https://doi.org/10.1038/s41598-022-08131-1 (2022).
Kappeler, P. M., Cremer, S. & Nunn, C. L. Sociality and health: Impacts of sociality on disease susceptibility and transmission in animal and human societies. Philos. Trans. R. Soc. Lond. B Biol. Sci. 370, 20140116. https://doi.org/10.1098/rstb.2014.0116 (2015).
Ezenwa, V. O. et al. Host behaviour–parasite feedback: An essential link between animal behaviour and disease ecology. Proc. R. Soc. B Biol. Sci. 283, 20153078. https://doi.org/10.1098/rspb.2015.3078 (2016).
Klein, S. L. Parasite manipulation of the proximate mechanisms that mediate social behavior in vertebrates. Physiol. Behav. 79, 441–449. https://doi.org/10.1016/S0031-9384(03)00163-X (2003).
LavistaFerres, J. M. et al. Social connectedness and movements among communities of giraffes vary by sex and age class. Anim. Behav. 180, 315–328. https://doi.org/10.1016/j.anbehav.2021.08.008 (2021).
VanderWaal, K. L., Wang, H., McCowan, B., Fushing, H. & Isbell, L. A. Multilevel social organization and space use in reticulated giraffe (Giraffa camelopardalis). Behav. Ecol. 25, 17–26. https://doi.org/10.1093/beheco/art061 (2014).
Sato, S. & Wood-Gush, D. G. Observations on creche behaviour in suckler calves. Behav. Process. 15, 333–343. https://doi.org/10.1016/0376-6357(87)90017-9 (1987).
Lecorps, B., Kappel, S., Weary, D. M. & von Keyserlingk, M. A. G. Social proximity in dairy calves is affected by differences in pessimism. PLoS One 14, e0223746. https://doi.org/10.1371/journal.pone.0223746 (2019).
Carslake, C., Occhiuto, F., Vázquez-Diosdado, J. A. & Kaler, J. Repeatability and predictability of calf feeding behaviors—Quantifying between- and within-individual variation for precision livestock farming. Front. Vet. Sci. 9, 827124 (2022).
Occhiuto, F., Vázquez-Diosdado, J. A., Carslake, C. & Kaler, J. Personality and predictability in farmed calves using movement and space-use behaviours quantified by ultra-wideband sensors. R. Soc. Open Sci. 9, 212019. https://doi.org/10.1098/rsos.212019 (2022).
Carslake, C., Occhiuto, F., Vázquez-Diosdado, J. A. & Kaler, J. Indication of a personality trait in dairy calves and its link to weight gain through automatically collected feeding behaviours. Sci. Rep. 12, 19425. https://doi.org/10.1038/s41598-022-24076-x (2022).
Planas-Sitjà, I., Deneubourg, J.-L. & Cronin, A. L. Variation in personality can substitute for social feedback in coordinated animal movements. Commun. Biol. 4, 469. https://doi.org/10.1038/s42003-021-01991-9 (2021).
Stockmaier, S., Bolnick, D. I., Page, R. A. & Carter, G. G. Sickness effects on social interactions depend on the type of behaviour and relationship. J. Anim. Ecol. 89, 1387–1394. https://doi.org/10.1111/1365-2656.13193 (2020).
Smith, L. A., Swain, D. L., Innocent, G. T., Nevison, I. & Hutchings, M. R. Considering appropriate replication in the design of animal social network studies. Sci. Rep. 9, 7208. https://doi.org/10.1038/s41598-019-43764-9 (2019).
Shin, D. H., Kang, H. M. & Seo, S. Social relationships enhance the time spent eating and intake of a novel diet in pregnant Hanwoo (Bos taurus coreanae) heifers. PeerJ 5, e3329. https://doi.org/10.7717/peerj.3329 (2017).
Acknowledgements
We would like to thank Emma Gayner and Nigel Armstrong for supporting the organization and running of the trial.
Funding
This research was founded by Innovate UK (project 103356) and by the Biotechnology and Biological Sciences Research Council, UK (project BB/S506758/1, BB/W020459/1).
Author information
Authors and Affiliations
Contributions
J.A.V.-D.: conceptualization, data curation, formal analysis, writing-original draft, writing—review and editing; F.O.: data collection, project administration, writing-review and editing; C.C.: data collection, writing-review and editing; J.K.: conceptualization, funding acquisition, project administration, resources, supervision, writing-review and editing. All authors gave final approval for publication and agreed to be held accountable for the work performed therein.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Vázquez-Diosdado, J.A., Occhiuto, F., Carslake, C. et al. Familiarity, age, weaning and health status impact social proximity networks in dairy calves. Sci Rep 13, 2275 (2023). https://doi.org/10.1038/s41598-023-29309-1
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-023-29309-1
- Springer Nature Limited
This article is cited by
-
Early detection of bovine respiratory disease in pre-weaned dairy calves using sensor based feeding, movement, and social behavioural data
Scientific Reports (2024)
-
Evidence of personality-dependent plasticity in dairy calf movement behaviours derived from automated data collection
Scientific Reports (2023)