key: cord-0864616-ahxdor8s authors: Bedoya-Pérez, Miguel A.; Ward, Michael P.; Loomes, Max; McGregor, Iain S.; Crowther, Mathew S. title: The effect of COVID19 pandemic restrictions on an urban rodent population date: 2021-06-21 journal: Sci Rep DOI: 10.1038/s41598-021-92301-0 sha: 7f44b5a76d0aebcdc3d06e6fa498ff2a587d1ec6 doc_id: 864616 cord_uid: ahxdor8s Shortly after the enactment of restrictions aimed at limiting the spread of COVID-19, various local government and public health authorities around the world reported an increased sighting of rats. Such reports have yet to be empirically validated. Here we combined data from multi-catch rodent stations (providing data on rodent captures), rodent bait stations (providing data on rodent activity) and residents’ complaints to explore the effects of a six week lockdown period on rodent populations within the City of Sydney, Australia. The sampling interval encompassed October 2019 to July 2020 with lockdown defined as the interval from April 1st to May 15th, 2020. Rodent captures and activity (visits to bait stations) were stable prior to lockdown. Captures showed a rapid increase and then decline during the lockdown, while rodent visits to bait stations declined throughout this period. There were no changes in the frequency of complaints during lockdown relative to before and after lockdown. There was a non-directional change in the geographical distribution of indices of rodent abundance suggesting that rodents redistributed in response to resource scarcity. We hypothesize that lockdown measures initially resulted in increased rodent captures due to sudden shortage of human-derived food resources. Rodent visits to bait stations might not show this pattern due to the nature of the binary data collected, namely the presence or absence of a visit. Relocation of bait stations driven by pest management goals may also have affected the detection of any directional spatial effect. We conclude that the onset of COVID-19 may have disrupted commensal rodent populations, with possible implications for the future management of these ubiquitous urban indicator species. Trapping success. Results are reported across the three periods under consideration, namely Pre-lockdown (October 1st, 2019 to March 31st, 2020), Lockdown (April 1st to May 15th, 2020) and Post-Lockdown (May 16th to July 31st, 2020). The mean number of active Multi-Catch rodent stations per day during the entire sampling period (1st October 2019 to 31st July 2020) was 36.96 ± SE: 0.91 (Pre-lockdown 25.90 ± SE: 0.63; Lockdown 59.00 ± SE: 0.21; Post-lockdown 50.38 ± SE: 0.93). A total of 38 locations were sampled across all three periods; 22 locations were sampled during two of the three periods and only four were sampled during a single period. A total of 851 rodents were captured during 305 days of deployment (mean: 2.79 ± SE: 0.469 per trap day). Overall, trapping success (i.e. number of captures and probability of capture) was affected by Period (i.e. Prelockdown, Lockdown and Post-lockdown) (χ 2 2 = 8.580; P = 0.014; Table 1 ). However, the overall number of rats caught per trap day did not differ between periods (Tukey's HSD: Pre-lockdown vs Lockdown, P = 0.881; Prelockdown vs Post-lockdown, P = 0.288; and Lockdown vs Post-lockdown, P = 0.165; Table 1 , Fig. 1a ). www.nature.com/scientificreports/ The probability of capture per trap day was highest Post-lockdown and lowest during Lockdown (Tukey's HSD: Pre-lockdown vs Lockdown, P = 0.459; Pre-lockdown vs Post-lockdown, P = 0.100; and Lockdown vs Postlockdown, P = 0.011; Table 1 , Fig. 1b) . Trapping success was also affected by date within each period (χ 2 3 = 9.810; P = 0.020; Table 1 ). Captures per trap and probability of capture per trap remained stable over Pre-lockdown (Conditional model: z = − 0.523; P = 0.601; Zero-inflated model: z = 0.700; P = 0.484; Table 1 Results are reported across the three periods under consideration, namely Pre-lockdown (October 2nd, 2019 to March 31st, 2020), Lockdown (April 1st to May 15th, 2020) and Post-Lockdown (May 16th to August 11th, 2020). Note the sampling period is slightly longer for bait station data than for trapping data. The bait stations employed by council provided only binary data on whether there had been a visit during the intervening period since the station was last checked. With routine bait station relocations by the Council's pest management contractors, a total of 661 unique locations were recorded during the entire sampling period. The mean number of rodent bait stations checked per day during the entire sampling period was 51.45 ± SE: 1.68 (54.66 ± SE: 2.05 Pre-lockdown; 41.30 ± SE: 3.93 during Lockdown; and 45.18 ± SE: 4.01 Post-lockdown). There were 376 locations sampled across all three periods; 50 locations were sampled only during two of the three periods and 235 were sampled during only a single period. Average rodent visitation per bait station per day, over 345 days of deployment was recorded as 0.516 ± SE: 0.052 (0 = Not visited and 1 = Visited). Rodent visitation per bait station per day was affected by period (χ 2 2 = 46.502; P < 0.0001; Table 2 ). The highest visitation per bait station per day was recorded Pre-lockdown (Tukey's HSD, P < 0.0001, Table 2 , Fig. 1c) , the lowest Post-lockdown (Tukey's HSD, P < 0.0001, Table 2 , Fig. 1c) , with visitation per bait station per day during Lockdown at an intermediate level (Tukey's HSD, P < 0.0001, Table 2 , Fig. 1c ). Rodent visitation was also affected Residents' complaints are reported across the three periods under consideration, namely Pre-lockdown (January 7th, 2019 to March 31st, 2020), Lockdown (April 1st to May 15th, 2020) and Post-Lockdown (May 16th to July 31st, 2020). Note the sampling period is slight longer than for both bait station and trapping data. The City of Sydney Council received 242 rodent related complaints during the entire interval under consideration; mean: 0.423 ± SE: 0.031 complaints per day. There were 161 (66.5%) complaints received through the Councils website, 72 (29.8%) through emails, and 9 (3.7%) by phone. Across the 33 suburbs and 23 localities within the Council, complaints were received from only 22 suburbs (Prelockdown 18 suburbs; Lockdown 10 suburbs; Post-lockdown 12 suburbs). Complaints were received from five suburbs during all three periods, eight suburbs during two periods and nine suburbs during a single period. The number of complaints per day received by the Council was not affected by period (χ 2 2 = 1.207; P = 0.547; Table 3 , Fig. 1d ) or date within period (χ 2 3 = 1.612; P = 0.657; Table 3 , Fig. 2c ). Multi-Catch rodent stations were operated within seven of the eleven Statistical Areas Level 2 (SA2) that contain the Council, whereas rodent bait stations were operated in all eleven SA2. Rodent related residents' complaints were made in all SA2 (Fig. 3) . For all three measures of rodent activity (trapping, bait station visitation and complaints) their mean centers and directional ellipses were approximately equivalent during the Pre-lockdown, Lockdown and Post-lockdown periods (Fig. 4a-c) . The spatial distribution of trapping success did not differ (i.e. significant correlation) between Pre-versus Post-lockdown periods (r SP 0.829, P = 0.021), but was different (i.e. correlation not significant) during Lockdown relative to both Pre-(r SP 0.270, P = 0.558) and Post-lockdown (r SP 0.679, P = 0.094). The spatial distribution of rodent visitation differed (i.e. correlation not significant) across all periods: Pre-lockdown relative to Lockdown (r SP 0.582, P = 0.060) and Post-lockdown (r SP 0.591, P = 0.056); and Lockdown rela- www.nature.com/scientificreports/ tive to Post-lockdown (r SP 0.518, P = 0.102). The spatial distribution of rodent related residents' complaints did not change (i.e. significant correlation) from Pre-lockdown relative to both Lockdown (r SP 0.791, P = 0.004) and Post-lockdown (r SP 0.709, P = 0.015) periods. However, the spatial distribution of rodent related residents' complaints did change (i.e. correlation not significant) from Lockdown to Post-lockdown (r SP 0.431, P = 0.186). Finally, the spatial distribution of the three measures (trapping, bait station visitation and complaints) were not correlated, except for trapping success and rodent visitation during Pre-lockdown (r SP − 0.775, P = 0.041). The current study used datasets supplied by the City of Sydney Council to examine the impact of a 6-week lockdown on three different measures of rodent activity, namely rodent captures, bait station visitation and resident complaints. The general trends for these three measures differed quite markedly (Tables 1, 2 and 3; Fig. 1 ). All three measurements were quite stable prior to COVID-19 restrictions (Fig. 2 ) but the introduction of Lockdown seemed to reduce captures and bait station visitation. These two measures then separated Post-lockdown (Tables 1 and 2 ; Fig. 2a,b) . Interestingly, the dynamic relationship between rodent captures and bait station visitation was not due to actual number of rodents captured per trap day, which remained the same between periods (Table 1 ; Fig. 1a ). Instead, this relationship was based on the probability of capture per trap day (Table 1 ; Fig. 1b ,c). These might be due to the high variability in the measures across the duration of each period, shown by the over time effects detected within each period (Tables 1, 2; Fig. 2 ), as well as the nature of the measurement and our analyses. Due to the over representation of zeros and overdispersion of the Multi-Catch rodent station data, the use of a Zero-inflated model was warranted 51, 52 . This type of model allowed us to detect any effects of COVID-19 restrictions on the number of rats caught in a particular trap per day, as well as the probability of capture of at least one rat in a given day. These two measurements might differ under certain circumstances. For example, if a small proportion of traps record high capture rates, while most record no captures, the mean number of captures per trap night might be the same as if most traps recorded a number of captures closer to the mean, and just a minority recorded no captures. Meanwhile, in this same example, the probability of capture would be low in the first scenario, since most traps did not record captures, and higher in the second scenario, since Fig. 1a ). Further supporting this idea is our spatial distribution analyses, where we recorded a slight change in the spatial distribution of rodent captures during Lockdown in comparison to Pre-lockdown and Post-lockdown (Fig. 4a) , which seems to suggest that some traps recorded higher trapping rates, while most recorded very low trapping rates. www.nature.com/scientificreports/ With the exception of rodent captures, our findings seem to contradict observations of rodent population after hurricanes 21, 22 . We hypothesize that this might be due to the undeniable temporal and physical differences between a climatic event and a pandemic. Climatic events are short-lived, with vast physical effects on the landscape, shifts in habitat characteristics, and increasing landscape heterogeneity 2,53 . In contrast, social restrictions were limited to closure of restaurants, cafes and other food venues 54 , causing a reduction in human-derived food resources where they have been plentiful before. Rodent captures per trap showed an abrupt spike during Lockdown, followed by a steep and rapid decline and a slow recovery during Post-lockdown (Table 1 , Fig. 2a ). In contrast, Lockdown seemed to have triggered a steep decline in rodent activity that continued Post-lockdown ( Table 2 , Fig. 2b ). We found no temporal changes in the number of rodent related complaints received by the council (Table 3 , Fig. 4 ). We found no directional spatial changes for any of the measurements between Pre-lockdown, Lockdown and Post-lockdown periods (Fig. 4) . However, the distribution of trapping success and rodent visitation at bait stations Pre-lockdown appeared spatially related, but this relationship was disrupted during Lockdown and continued to be disrupted Post-lockdown. Since the spatial distribution of trapping success only changed during Lockdown, relative to Pre-and Postlockdown spatial distributions, the disruption in the relationship between trapping success and rodent visitation seems to be due to the change in spatial distribution in rodent visitation during Post-lockdown. Rodent visitation spatial distribution changing across all periods, seems to suggest that this measure of rodent abundance did not recover from the disruption suffered during Lockdown. Commensal rodents show high levels of neophobia 55, 56 and taste aversion 2,53 resulting in high levels of 'trapshyness' 57,58 and low bait acceptance 59, 60 . However, a reduction in food resources might have driven animals to engage in "bold" behaviors during foraging whilst in a lower physiological state 61, 62 . These hunger-driven behaviors might explain reports of rats feeding in close proximity to humans 31, 45, 46 as well cannibalism 31, 38 . Ultimately, hunger might have caused these animals to overcome their neophobia and taste aversion, resulting in a decrease in trap shyness potentially driving an increase in mortality by electrocution. However, under this premise, we expected that rodent activity at bait station would reflect captures and spike, yet we did not find that. One possibility is that the reduction in food resources was not enough for animals to overcome their taste aversion towards the commonly used rodenticides at the bait station. In contrast, Multi-Catch rodent stations are baited with non-toxic food attractants, thus taste aversion might be unlikely. Another possibility is the difference in resolution of the data between Multi-Catch rodent stations and bait stations. Rodent visitation at bait station was recorded as "not visited" or "visited", collapsing the potential variability present in rodent visitation in a binary measure. Thus, a record for a peak in visitation (e.g. increase signs of rodents and higher levels of bait taken from the bait stations) could have effectively being lost by grouping them at the same level as reduced, yet present, visitation (e.g. limited signs of rodents and bait taken). However, this does not explain why rodent related residents' complaints did not change between periods or over time within each period. Rodent related residents' complaints seem to be completely disassociated from rodent captures and activity, remaining stable over time and between periods, except for a change in spatial distribution observed Post-lockdown. This is contrary to what has been reported during periods of no disturbance 42 ; and during COVID-19 41 . One possible explanation is that, during the Lockdown period, most people remained home social distancing, with many leaving the Council to neighboring areas, similar to counter-urbanizations 20 . With less people within the Council, the chances of rats sightings would have been reduced, thus the lack of change in the number of www.nature.com/scientificreports/ rodent related complaints might not reflect the rodent population, but might be an artefact of less people commuting and occupying public spaces. Furthermore, a decrease in resources by the closure of restaurants and cafes, might have driven rodents to move from public spaces to private residences where food waste was still available. People that then experienced an increased in rodents' sightings within their residence, might have contacted pest controllers directly and not the Council. Similarly, prior to COVID-19 restrictions, a single rat sighted around a restaurant café or public space, could have been reported by a high number of customers and residents. In contrast, during the Lockdown period, several rats sighted within a resident would incite a single complaint to the Council. Previous research on the relationship between the number of rodent related residents' complaints and the actual rodent population, show a direct relationship between the two 42 , but do not account for disruptions in human behavior such as the ones brought up by COVID-19. More complex responses in rodent related residents' complaints, in relationship with COVID-19, have been reported recently 41 and are in concordance with our findings. A higher mortality due to a decrease in carrying capacity might explain the activity decline that we found during the lockdown period and in captures later on during the same period 63, 64 . It is highly unlikely that the peaks in rodent captures would be due to an increase in the rodent population, given that the lockdown period lasted only 45 days. It is also important to note that we classified lockdown as the short period during which COVID-19 restrictions were at their peak, with cancellations of all social gatherings, mandatory closure of all non-essential businesses including restaurant and cafes 54 . Both the pre-lockdown and the post-lockdown periods encompassed the gradual increase and decrease of these restrictions over several weeks 54 . Therefore, even rats, which are known for their prolific reproduction 65,66 , would not be able to reproduce and mature in such a limited time frame and even less with disruptions on human behavior still present. The recovery in the population is therefore expected to be more gradual, like the steady but slow increase in rodent captures we found in the post-lockdown period. Interestingly, rodent activity again did not mirror the rodent captures data post-lockdown. As argued above, this difference might be a consequence of the nature of the data collected. If the peak in rodent activity was indeed due to abnormal foraging behavior caused by starvation followed by a population reduction, it is highly possible that the lockdown acted as a genetic bottleneck. Previous research has shown that, after such a mortality event, the genetic variation within the remaining population could be up to 90% lower than the original population 67 . Given that our data did not cover several years, we were unable to account for natural seasonal cycles in the rodent population. Several studies have shown that urban rodent populations follow a seasonal gradient that reflect both human changes in behaviors and temperature 17, 42, 68, 69 . Colder months seem to trigger lower rodent activity, that then increase towards spring and peaks in summer 42, 68, 69 . During harsh winters, rats have been reported to move from outdoors to indoors in search of food and warmth 70 , and this behavior has been linked to an increase in rodent related resident's complaints 17, 71 . Our Pre and Post-lockdown multi-catch station data seems to support this, but not so our bait station data. However, the lowest temperatures recorded during this study, were recorded in July during Post-lockdown (i.e. 7 °C 72 ), when trapping success was not the lowest and was instead steadily increasing. It is possible that in a subtropical City such as Sydney (average minimum temperature 15.7 °C 72 ) the effect of seasonal changes in temperature might not be as strong as that detected in laboratory studies 68, 69 and more temperate cities 42 . Additionally, it has been well documented that cities are "heat islands" that experience significantly milder winters than surrounding areas 73 . This might be more pronounced in coastal cities like Sydney. Seasonal changes in rat activity have also been linked to changes in human behavior, and not solely a respond to the change in temperature, with people spending more time outdoors during the warmer weather, thus increasing sightings and resource availability 17, 42 . Thus, the abrupt reduction in human activity during the lockdown, might have acted as an early onset of winter. Moreover, the expected seasonal changes in rodent activity cannot explain the abrupt increase and decline in captures, nor the accelerated decline in rodent visitation during Lockdown. Therefore, we argue that the effects we report are solely due to the changes in human behaviors, and unintended effects on the rodent population, elicited by the COVID-19 restrictions. We found no evidence of directional spatial changes driven by the Lockdown. This supports the findings Parsons et al. reported from Warsaw, Poland but contrast with their results from New York City and Tokyo 41 . They suggested that COVID-19 Lockdown measures trigger an increase in rodent movement and potential massive migrations, based on the increased association of rats and food service establishments and the formation of new hotspots of rat sightings in New York City 41 . However, the level of rodent migration Parsons et al. 41 suggests-i.e. tenths of kilometers-is difficult to reconcile base on the well-known site fidelity pest rodents species show 74 . However, this does not negate the possibility that rodents might have move from areas of normally abundant resources that were suddenly reduced-i.e. restaurants and cafes-to areas where some limited level of resources remained-e.g. private residences. In fact, although we did not detect any directional spatial changes, we did detect changes in the spatial distributions of our rodent abundance measures. Parsons et al. 41 , suggest that the pattern of movement reported, was not recorded in Warsaw, potentially because of the lack of restaurant clusters in that city, a situation that may be similar to the one in Sydney. The City of Sydney Council is not comprised by distinct clusters of offices and residents, with most buildings being of "dual use", with business at ground floor and residential apartments above. Without distinct residential and business suburbs within the City of Sydney Council, rats might move very short distances to small pockets within the surrounding area in search of resources, thus long-distance directional migration would not be detected. Moreover, is crucial to recognize the limitations of the data we used. Both Multi-Catch and bait rodent stations were sometimes removed or relocated to target "problem" areas within the Council based of the Council's pest management objectives. This process might have removed any spatial effect. Therefore, although we did not detect any obvious directional shifts in spatial distribution, if such shifts did occur, they were most likely subtle, and we were unable to detect them. Although the risks of commensal rodents to be infected or transmit SARS-CoV-2 are low 75 , we know that these animals pose other health risks 2,7-14 . Thus, an increase in rodent-human interactions has the potential to place further strains on health systems around the world. Fortunately, our data seems to suggest the increase Scientific Reports | (2021) 11:12957 | https://doi.org/10.1038/s41598-021-92301-0 www.nature.com/scientificreports/ in rodent-human interactions, as reported by the media, might be an overstatement. Undoubtedly, the onset of COVID-19 might have disrupted not only human behavior, but also commensal rodent populations, yet the implications for the future management of these species is still uncertain. The disruptions caused by COVID-19 restrictions to the rodent population seem to differ depending on the measured used. Our data illustrates how two different control methods (i.e. lethal traps and bait stations) can show similar patterns, and potentially have similar efficacy, during normal conditions. However, an abrupt change in human behavior can disrupt this efficacy and possibly change the characteristics of the individuals targeted by each method. Although it is too early to determine if these disruptions would have long term effects on management outcomes, the different patterns reported for lethal traps and bait stations highlights the need to follow integrated pest management (IPM) frameworks that do not rely on a single control methods 76 . Study area. The City of Sydney Council (hereafter Council) is the largest city, by population, in Australia, with 240,229 residents 77 . It comprises a highly urbanized part of the Greater Sydney region and includes the Central Business District of Sydney and many of Sydney's major tourist attractions (e.g. the Opera House). It borders Port Jackson in the north, the Woollahra Municipal Council area and Randwick City in the east, the Bayside Council area in the south, and the Inner West Council area in the west 77 . Sydney has a humid subtropical climate (average maximum = 21.3 °C; average minimum = 15.7 °C; 72 . The Council is composed of 33 suburbs and 23 localities. In Australia, suburbs are defined as geographical subdivisions used for address purposes and refer to portions of a city that can include inner-city, outer-metropolitan, and industrial areas. The Australian definition of suburb is more alike the American and British definitions of "district" or "neighborhood". Localities are defined as historically unrecognized geographical units that due to common informal used, and later government decree; official boundaries were established and are currently recognized geographical features. Data sourcing. All data used in this research were obtained from the Council. As part of Council's ongoing rodent control operations, pest management contractors have deployed multi-catch rodent stations as well as rodent bait stations across the Council. The Council conducts pest management operations only on Council property and outdoors. Rodent captures and activity are recorded regularly, and the data are stored by the Council. The Council also receives residents' complaints through phone calls, emails or through electronic complaint forms found on the Council's website. These complaints are compiled and stored by the Council. Rodent pest management by the Council targets brown rats (Rattus norvegicus), and black rats (R. rattus); the former being the most common species found in the urban environment. Common house mice (Mus musculus) are also found within the council, but they seldom occur outside of buildings, and their control is considered the responsibility of property owners and managers. Due to unreliable identification by pest management contractors and general public, the records used for this study do not include species specific data (i.e. R. rattus vs R. norvegicus). A subsample of 95 rat carcasses obtained from live trapping and multi-catch rodent stations across the Council suggests R. norvegicus to be the dominant species within the council (i.e. 88 R. norvegicus and 7 R. rattus). patented rodent trap design 78 . This trap consists of a trigger mechanism that kills the animal by an electric current. The trap has a built-in programmable computer with a SIM card, enabling it to communicate via the mobile network when it has been activated. This trap can catch multiple animals (eight maximum), before it needs to be serviced. Under a pest management contract between the Council and Flick Anticimex Pty Ltd, 20-60 multi-catch rodent stations were deployed outdoors on public places and Council own land from October 2019 to July 2020. Deployment was non-random and guided by strategic pest management priority zoning. Multi-catch rodent stations were sometimes removed or relocated, whenever they were damaged or if trapping success did not reflect the Council's pest management goals (i.e. zero captures for 4 weeks). These stations were baited with barbeque grease and commercially available rodent attractants The Council received monthly reports from Flick Anticimex Pty Ltd over the deployment interval that contained the number of traps active, the location in latitude and longitude coordinates of each station and the number of captures per day per each trap. Rodent bait stations dataset. Additionally, 942 bait stations (PROTECTA EVO Ambush and PRO-TECTA LP, Bell Laboratories, Inc.) were deployed outdoors on public places and Council own land from September 2019 to August 2020. Deployment was non-random and guided by strategic pest management priority zoning. Bait stations were sometimes removed or relocated, whenever they were damaged or if rodent activity did not reflect the Council's pest management goals (i.e. low to no activity for 4 weeks). These stations were baited with commercial poisoned baits (Bromadiolone: Contrac Blox and Contrac Soft Bait; Brodifacoum: Ditrac Blox; Difethialone: Generation Block and Rodilon Soft Block; Flocoumafen: Storm Secure Block and Storm Soft Bait). Baits were randomly rotated at each station, to prevent rodents developing aversion to any bait. Each station was checked regularly (mean: 10.56 Days ± SE: 0.06) and scored according to the rodent visitation i.e. low: no bait consumed and no visual signs; or high: bait consumed and visual signs present. Following strategic pest management principles, bait station with consistent low activity score were relocated. The location for each bait station was recorded in UTM coordinates to facilitate spatial analyses. Rodent related residents' complaints dataset. Murray, et al. 42 previously showed that the number of rodent related residents' complaints can be used as an estimate of rat relative abundance across diverse urban landscapes. Later Parsons et al. 41 www.nature.com/scientificreports/ estimate changes in rodent pest populations during COVID-19 restrictions. However, the relationship between rodent related residents' complaints has not been validated during disruptions in human behavior such as the ones created by the COVID-19 pandemic. Therefore, we accessed all rodent related complaints made to the Council from January 2019 to August 2020 and included these data in our analyses. Complaints were received through phone calls, emails or through electronic complaint forms found on the Council's website. All complaints contained the date and street address. Identifying information was removed from the complaint dataset, with street address transformed to UTM coordinates to facilitate spatial analyses, and suburb used for statistical analyses. Following the rapid increase in COVID-19 cases at the beginning of 2020, the New South Wales State Government enacted a series of preventative measures to limit the spread of the disease. These preventative measures included limits in the number of attendees at social gatherings, mandatory closure of all non-essential businesses, restrictions to only operate as "take-away" for restaurant and cafes, and border closures with other Australian States and Territories. We used the publicly available timeline of these measures 54 , to classify the datasets into three "Periods". Pre-lockdown was defined as the period prior to March 31st, 2020; the Lockdown was defined as the period from the April 1st to May 15th, 2020; and Post-lockdown was defined as the period from May 16th onwards. Statistical analyses. To explore whether there was any effect of COVID-19 restrictions overall on pest rodent population and residents' perception within the Council, we performed statistical analyses in R 4.0.2 79 . Each dataset had a different distribution and were at slightly different spatial scales, hence the need for different models. Due to the over representation of zeros and overdispersion, the Multi-Catch rodent station dataset was analyzed by a Zero-inflated Generalized Linear Mixed Model (GLMM) using the function glmmTMB from the package "glmmTMB" version 1.0.2.1 80 with a negative binomial error distribution. Zero-inflated models are used for count data that are over dispersed and are characterized by an excess of zeros 51, 52 . The data distribution used for zero-inflated models combines the negative binomial or Poisson error distributions and the logit error distribution functions, effectively modelling count values separately from the excess zeros which are treated as binomial data (i.e. 0 or 1) 51,52 . Therefore, model outputs for zero-inflated models include analyses of count data, in our case number of animals captured, and binomial data, in our case probability of capture. The rodent bait station dataset was analyzed by a GLMM with a binomial error distribution, using the function glmer from the package "lme4" version 1.1.23 81 . The rodent related residents' complaints dataset was analyzed by another GLMM, using the functions lmer, from the package "lme4" version 1.1.23 81 . With the exception of the models constructed to test the rodent bait station dataset, residual plots and the Pearson's dispersion test were used to identify the best distribution and link for each model 82 . Each model aimed to test the effects of COVID-19 restrictions on the number of rodent captures per day (Multi-Catch rodent stations), the level of rodent visitation (Rodent bait stations) and residents' reporting of rodent activity (number of complaints). Period (i.e. Pre-lockdown, Lockdown and Post-lockdown), numerical date (day as integer starting at 1 to last sampling day per data set, when each data point was collected), and numerical date nested within period (as each date value only occurred within a particular period) were included as fixed factors. The model testing the number of rodent related residents' complaints initially included the mean of communication (i.e. email, council website or phone call) as a covariate, due to lack of significance (P > 0.50) this covariate was later removed in order to simplify the model 83 . To account for intrinsic differences in rodent captures, visitation and number of complaints based on location, each model included location (i.e. trap or bait station coordinates, or the suburb where complaint was received from) as the only random factor. Additionally, in the case of the Multi-Catch rodent station and rodent bait stations, to account for differences in sampling effort due to variable number of stations deployed across the sampling period, the number of active Multi-Catch rodent station or bait stations checked per day were included in the models as offsets. To generate P-values, Wald Chi-square tests were applied to all models using the function Anova from the package "car" version 3.0.9 84 . Post-hoc pairwise comparisons with Tukey adjustments were carried out by the functions emmeans, and pairs from the package "emmeans" version 1.5.0 85 , and the function cld from the package "multcomp" version 1.4.13 86 . Graphs were constructed using package "ggplot2" version 3.3.2 87 . The spatial distribution of total rodent captures (Multi-Catch rodent stations), the level of rodent visitation (Rodent bait stations with high visitation) and residents' perceptions of rodent activity (total number of complaints) were visualized by creating dot maps based on latitude and longitude or UTM and the Inner Sydney and Eastern Suburbs-North polygons of the Statistical Areas Level 3 (SA3) dataset set 2016 (Geographic Datum of Australia 1994). Data were projected in UTM 56S using ArcGIS 10.5 88 . For each dataset overall and for the three study periods, mean centers and directional ellipses were calculated (Spatial Statistics. ArcGIS 10.5. ESRI). Rodent captures, visitation and complaints data were summed to SA2 areas: the 10 areas which make up Inner Sydney SA3 and the adjacent Paddington-Moore Park SA2 which lies within SA3 Eastern Suburbs-North. The correlations (r SP ) between these data by SA2 were calculated on SPSS v24 89 . Most of the data that supports the findings of this study are available from Dryad 90 but restrictions apply to the availability of the rodent related residents' complaints data, which were used under license for the current study, and so are not publicly available. Data are however available from the authors upon reasonable request and with permission of the Council of the City of Sydney. Rodent-borne diseases and their risks for public health The Year of the Rat ends-Time to fight hunger! The role of rodents in emerging human disease: Examples from the hantaviruses and arenaviruses The Story of Rats: Their Impact on Us, and Our Impact on Them The economic impact of commensal rodents on small businesses in Manhattan's Chinatown: Trends and possible causes Rat-borne diseases at the horizon. A systematic review on infectious agents carried by rats in Europe Detection of zoonotic pathogens and characterization of novel viruses carried by commensal Rattus norvegicus in New York City Preliminary survey of ectoparasites and associated pathogens from Norway rats in New York City Old world hantaviruses in rodents in New Orleans Rodent-borne Bartonella infection varies according to host species within and among cities Rat lungworm infection in rodents across post-katrina Transmission ecology of rodent-borne diseases: New frontiers Rodent reservoirs of future zoonotic diseases Mice, rats, and people: The bio-economics of agricultural rodent pests Update on the environmental and economic costs associated with alien-invasive species in the United States The secret life of the city rat: A review of the ecology of urban Norway and black rats (Rattus norvegicus and Rattus rattus) 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 Zoonotic Diseases Rodent control in urban areas: An interdisciplinary approach Rodent assemblage structure reflects socioecological mosaics of counter-urbanization across post-hurricane Katrina New Orleans. Landsc. Urban. Plann. 195, 103710 Invasive rat establishment and changes in small mammal populations on Caribbean Islands following two hurricanes Can rodent outbreaks be driven by major climatic events? Evidence from cyclone Nargis in the Ayeyawady Delta De-urbanization and zoonotic disease risk Abandonment, ecological assembly and public health risks in counterurbanizing cities Disturbance, reassembly, and disease risk in socioecological systems Higher mosquito production in low-income neighborhoods of Baltimore and Washington, DC: Understanding ecological drivers and mosquito-borne disease risk in temperate cities COVID-19 lockdown allows researchers to quantify the effects of human activity on wildlife Why more rats are being spotted during quarantine Sydney braces for rat 'plague' after Covid-19 forces hungry rodents to turn to cannibalism The Pest Control Sydney sector warns of increase of rat activity due to COVID-19 shuts down food supply Rats on the rise as shutdown cuts their food supply The Age (Nine Entertainment Co Health is associated with antiparasite behavior and fear of disease-relevant animals in humans They're always there": Resident experiences of living with rats in a disadvantaged urban neighbourhood Exposure to urban rats as a community stressor among low-income urban residents Ecology and Evolution Among Diverse Taxa The pandemic of social media panic travels faster than the COVID-19 outbreak A mixed methods approach to exploring the relationship between Norway rat (Rattus norvegicus) abundance and features of the urban environment in an inner-city neighborhood of Vancouver Rats and the COVID-19 pandemic: Early data on the global emergence of rats in response to social distancing Public complaints reflect rat relative abundance across diverse urban neighborhoods Preventing problematic internet use during the COVID-19 pandemic: Consensus guidance Social media use during social distancing PMPs re-strategize rodent control in response to COVID-19 pandemic As Japan fights coronavirus with shutdowns, rats emerge onto deserted streets Naïve, bold, or just hungry? An invasive exotic prey species recognises but does not respond to its predators Ethanol concentration in food and body condition affect foraging behavior in Egyptian fruit bats (Rousettus aegyptiacus) State of emergency: Behavior of gerbils is affected by the hunger state of their predators Complex state-dependent games between owls and gerbils Beginner's Guide to Zero-Inflated Models with R (Highland Statistics Limited Zero Inflated Models and Generalized Linear Mixed Models with R (Highland Statistics Limited Changes in rodent communities according to the landscape structure in an urban ecosystem Experiments on "neophobia" in wild and laboratory rats Activity, exploration, curiosity and fear: An ethological study Control of Rats and Mice (Agricultural Extension Service The reactions of common rats to four types of live-capture trap Behavioural resistance towards poison baits in brown rats Foraging behaviour of wild rats (Rattus norvegicus) towards new foods and bait containers Poison-induced neophobia in rats: Role of stimulus generalization of conditioned taste aversions Flavor-illness aversions: Potentiation of odor by taste in rats Density dependence as related to life history strategy Persistence and extinction in spatial models with a carrying capacity driven diffusion and harvesting The reproduction of the wild brown rat (Rattus norvegicus Erxleben) The rate of recovery of decimated populations of brown rats in nature Significant genetic impacts accompany an urban rat control campaign in Salvador Behavioral strategies in the cold: Effects of feeding and nesting costs Ambient temperature and food costs: Effects on behavior patterns in rats Evaluation of urban rodent infestations-An approach in Nepal Rat fields, neighborhood sanitation, and rat complaints in Climate statistics for Australian locations. Australian Bureau of Meteorology The impact of urbanization and climate change on urban temperatures: A systematic review Rats about town: A systematic review of rat movement in urban ecosystems Functional and genetic analysis of viral receptor ACE2 orthologs reveals a broad potential host range of SARS-CoV-2 Ecologically-Based Management of Rodent Pests-Re-evaluating Our Approach to an Old problem Australian Bureau of Statistics Anticimex Innovation Centre A/S, assignee. A trap R: A language and environment for statistical computing v. 3.6.1 (R Foundation for Statistical Computing glmmTMB balances speed and flexibility among packages for zero-inflated generalized linear mixed modeling Fitting linear lixed-effects models using lme4 Mixed Effects Models and Extensions in Ecology with Data Analysis with SPSS: A First Course in Applied Statistics An R Companion to Applied Regression Emmeans: Estimated marginal means, aka least-square means Simultaneous inference in general parametric models Elegant Graphics for Data Analysis 2nd edn IBM SPSS Statistics for Windows v. 24.0 (IBM Corp Flick SMART multi-catch rodent station and bait station data sets: Council of the city of Sydney This research was funded by the Council of the City of Sydney (2019/609066) and conducted with permission from the University of Sydney Animal Research Authority 2020/1725. We thank Kurtis Boys for his assistance in obtaining access to data used in the research. 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