Pet treatments could be harming freshwater life

The use of flea treatment on pets could be causing problems in English rivers and lakes. The chemicals used in the treatments are toxic to freshwater invertebrates and have been detected in rivers across England despite severe restrictions on agricultural use since 2018. Reducing the risk posed by these chemicals requires improved scientific knowledge, better monitoring and stricter regulatory management. Vets and pet owners may have a very important part to play because they can help by simple changes in behaviour.


Authors: Hamish Duncalf-Youngson, Nicole Stasik, Dr Dania Albini, Dr Leon Barron, Dr CM (Tilly) Collins, Professor Alex Dumbrell, Dr Michelle Jackson, Professor Andrew Johnson, Dr Rosemary Perkins, Dr Andrew Prentis, Rhys G. G. Preston-Allen, Professor David Spurgeon, Clodagh Wells, Professor Guy Woodward.



Background

UK freshwater habitats represent areas of high biodiversity that provide essential ecosystem services for provision of drinking water, food production and flood prevention. It is vital we protect them from the most harmful of human impacts (1,2). Chemical pesticides - insecticides in particular - that are harmful to ecosystems are often detected in rivers across England.

Two of the most frequently used chemicals in pet flea treatments - imidacloprid and fipronil - were found in 66% and 99% of samples from 20 English rivers between 2016 and 2018, respectively (3); this, despite both chemicals being banned for outdoor agricultural use by 2018 (4,5) and no recorded usage since 2016 (6). However, they are still widely used in pet treatments. Environment Agency monitoring of English rivers shows that these chemicals are still frequently detected despite the large‑scale reduction in agricultural use*. For instance, recent research suggests that the principal source of river contamination from imidacloprid may now be from pet treatments (3,7,8) (Fig. 1).

* Northern Ireland, Scotland and Wales each have their own separate water monitoring agencies; this article focuses on England as a case study.

Figure 1: Distribution of fipronil (blue) and imidacloprid (red) at potentially harmful concentrations in rivers across England. The points are sites in English rivers at which fipronil and imidacloprid were detected in excess of their respective freshwater predicted no-effect concentration (PNEC) values from liquid chromatography mass spectrometry (LC-MS) analysis between 2016-2022 (7). The PNEC in fresh water for fipronil is 0.77 ng/L and 13 ng/L for imidacloprid (9). Between 2016 and 2021, 121 and 64 out of 284 total sites sampled had concentrations of fipronil and imidacloprid exceeding their respective PNEC values.


A brief history of pesticides and current environmental contamination

Pesticides have been used on an industrial scale worldwide since the 1960s, mainly in agriculture to suppress or eradicate invertebrate populations that reduce crop yield, or which are hosts or vectors of disease (10,11). There are often, however, unintended detrimental consequences for non-target species (12). Chemicals such as dichlorodiphenyltrichloroethane (DDT) and dieldrin (used as ‘sheep dip’) were some of the first to gain widespread notoriety for their devastating impact on natural ecosystems and, in some instances, their effect on human health (13). These chemicals were subsequently banned in many countries during the 1970s and 1980s (14-16).

More recently, many of the subsequent generations of chemicals, such as imidacloprid and fipronil, have also been identified as having potentially harmful impacts in natural ecosystems. These two chemicals in particular have been at least partially implicated in global declines of bee populations (17-19), and they are also toxic to many other non-target species of invertebrates, as well as birds, fish and other vertebrates (20). Both have since been banned from outdoor agricultural use in the European Union (4,5) and the UK, but these and other chemicals are still used in large quantities as veterinary pesticides (Figs. 2 & 3), including a broad range of parasiticide products used to prevent or treat parasite infestations in pets (21). Tick and flea infestations in pets can also increase the potential for human infections, for example of Cat Scratch Disease (Bartonella henselae) (22, 23), although instances of transmission from pets are generally considered rare, with no recorded cases of Bartonellosis reported in the UK in 2022 or between January and June 2023 (latest published reports) (24-27). The chemical treatments used are compounds that are designed to be highly toxic to the target organisms at low concentrations, which is why they are so effective when used to control pests and parasites8, but it also means they can be harmful to certain wildlife if they end up in natural ecosystems.

Figure 2: Seven of the most commonly used parasiticides in the UK and their main application method in 2020 (Veterinary Medicines Directorate (VMD) Freedom of Information request, 2022).

Following restrictions on agricultural practices in 2018, veterinary parasiticides in waste water pathways have been implicated as a potentially important source of the current presence of fipronil and imidacloprid in surface waters (3,32,33). ‘Down-the-drain’ passage following spot-on application to pets has recently been confirmed as a viable pathway (34,35). Another potential contamination route is via freshly treated pets swimming in water or excreting near a water course (Fig. 4).

Despite improvements in the environmental monitoring of these chemicals, sampling effort remains limited: in 2021, of the 426 routine water samples collected across England for LC-MS analysis, only 40% were tested for imidacloprid, yet over half of those had detectable levels of the compound (7). The presence of these chemicals is worrying as they have the potential to cause detrimental effects once they enter freshwater habitats, irrespective of whether they were originally used on pets or in agriculture (36,37).


Box 1: Common Types and Usages of Veterinary Parasiticides (Sales values taken from a Freedom of Information request to the Veterinary Medicines Directorate 2022)

  • Imidacloprid is a neonicotinoid insecticide that affects the nicotinic acetylcholine receptor (nAChR) of blood-sucking insects and fleas (28). Over 4,200 kg was sold in the UK in 2017. 

  • Fipronil is a phenylpyrazole parasiticide that disrupts the central nervous system of fleas and ticks (29). Over 1,800 kg was sold in the UK in 2017.

  • Fluralaner is an isoxazoline acaricide and insecticide that inhibits the function of nerve receptors in fleas and ticks (30). Over 1,500 kg was sold in 2017 in the UK in 2017.

  • Flumethrin is a pyrethroid ectoparasiticide that alters the nerve functioning of fleas, ticks, and lice (31). Over 300kg was sold in the UK in 2017. 


Potential ecological impacts

Finding veterinary parasiticides in freshwater ecosystems is a concern, largely due to the harm they might do to vulnerable non-target species3, (38-41). Fresh waters depend on invertebrates for a range of ecosystem processes and services, including nutrient cycling, which are critical for preserving ecosystem health (42). These species are also food sources for many fish, amphibians, and other predators, so impacts on these assemblages could ripple through the food web and the whole ecosystem (43).

The wider ecological impacts of veterinary parasiticides remain under-explored, although an increasing number of studies point to their potential to harm aquatic communities (8). Research suggests that exposure to concentrations equivalent to less than a teaspoon of either imidacloprid or fipronil in an Olympic-sized swimming pool can reduce richness and abundance, cause downstream drift, and increase mortality in key invertebrate species (37,38,44-47).

Parasiticides can affect ecosystems in a number of different ways, ranging from direct and acute toxicity, where they can be lethal to certain species from just a single exposure event, to often more subtle chronic toxic effects that may impair feeding behaviour, growth or reproduction over longer time scales (48-50). Both can harm the wider ecosystem due to knock-on or cascading effects through the food web, which may persist even long after the chemical pollutant itself (51-53).

If we are to protect and manage freshwater ecosystems more effectively, we need to understand how the effects of such chemicals move through food webs in space and time and whether the risks they pose may be exacerbated in combination with other types of pollution or amplified by climate change. In the absence of this more complete understanding, caution should be exercised in the use of highly toxic chemicals that can spill into our natural ecosystems.

Patterns of parasiticide use

To give a sense of scale to the potential problem of parasiticide pollution, there are about 23 million dogs and cats in the UK (54). It is common practice among many veterinary practitioners to prescribe preventative treatment to reduce the risk of parasite infection, often in the absence of clinical evidence of parasites in, or on, the animal (55,56). Moreover, many treatments containing insecticides are freely available for purchase without prescription, supporting regular prophylactic use as recommended by the manufacturers.

Figure 3: Patterns of imidacloprid usage in UK agriculture and total sales in domestic veterinary pet parasiticide products before and after the 2018 ban on outdoor use in the European Union (4). The ‘pre-ban’ data is taken from 2009 and ‘post-ban’ from 2019. Volume of agricultural usage of imidacloprid was obtained from the Food and Environment Research Agency (6). As not all crop types are surveyed each year, it is not possible to plot the total usage in any individual year but the figures provided give an indication of usage patterns over time. Arable crops, which had the largest agricultural usage, were not surveyed in 2009, meaning that actual usage may have been greater. Data obtained from the Veterinary Medicines Directorate (VMD Freedom of Information request, 2022).


The British Veterinary Association now advises against blanket treatment in favour of risk assessment and/or testing (56). However, the lack of robust data surrounding incidence and health impacts of pet-borne parasites on dogs, cats and people (57-59) means there is little agreement on how to assess the health risks associated with the presence of parasites.

There is currently limited supervision over the number of treatments sold to pet owners, or whether the correct chemical and dose are used, as no prescription is required to obtain many of these products (56,60-62). Though the quantity used for each application is small (only 40 to 400 mg (63) the widespread use, given the millions of pets that reside in the UK, can lead to substantial total usage volumes (Figs. 2 & 3).

Figure 4: Potential routes by which pet parasiticides could enter ponds, lakes and rivers.


Future regulation and research

Given the irrefutable evidence of ongoing contamination of fresh waters in England and associated potential for ecological harm, there is a strong case for a comprehensive review of how pet parasiticide chemicals are used and regulated (64).

Recommendations for parasite treatments should continue to discourage prophylactic ‘blanket’ treatment and consider how factors such as pet lifestyle (e.g., urban or rural, free-roaming or housed), and seasonal variation in parasite risk could be used to reduce the chances of environmental harm, advising more proportionate, better targeted treatment (56). There is a case for considering whether over-the-counter access to such treatments should be restricted, with a full explanation provided by an awareness campaign, endorsed by veterinary practitioners.

Aside from the risks to the environment from unintended exposure, reducing unnecessary usage would reduce costs for the pet-owner and could help to limit the development of resistance, a problem now well recognised with antibiotics and pesticides in general and with parasiticides in horses and livestock in particular (65,66). It is also important to ensure that appropriate regulatory protocols are developed and implemented for the next generation of parasiticides that come to market, especially if we are to avoid simply repeating the mistakes of the past but with a new suite of chemicals.

It is likely that parasiticide treatment sales are at least partially driven by marketing, much of which focuses on how the products help to prevent or deal with the health risks associated with parasites (54). However, there is a dearth of evidence surrounding the incidence rates of parasite-related disease in humans and pets in the UK (56‑58). Further research is needed to quantify this risk and identify appropriate and proportionate mitigation strategies (67,68). This, combined with the pressing environmental threat, means that there is insufficient evidence-based justification for the large volume of veterinary parasite treatments sold and used on an annual basis (Fig. 2).

Advertisement of veterinary prescription-only medicines is restricted exclusively to professionals, but parasiticides with less stringent prescribing restrictions may be advertised more widely (56). A regulatory change to make all veterinary parasiticides prescription-only might reduce use but would be difficult to achieve in practice without support from veterinary professionals and manufacturers. Discouraging or stopping monthly subscription parasiticide schemes altogether, in favour of more targeted risk-based treatments might be a more effective approach of reducing environmental residues, whilst maintaining pet and human health.

Further research is needed to improve our understanding of the precise origin and the full scope of ecological impacts of these chemicals in UK fresh waters, from genes to entire ecosystems (69). If domestic dosing of pets is indeed confirmed as a major source, a review of current regulations and policy could help to mitigate future impacts on our natural ecosystems. Research should focus on identifying optimal usage for maintaining both human and pet health, whilst minimising environmental impact. This is a major challenge but one that needs to be grasped urgently to ensure that there is a strong and reliable evidence base on which to base future actions and potential regulatory change, both within and beyond the UK.


Actions that pet owners can take to reduce the environmental impact of pet parasiticides:

  • Check your pets regularly for parasites and ask your vet clinic for help with assessing the risk for them.

  • Consider only treating parasites if there is clear evidence of a high risk of infection or risk to the health of your pets or the people around them.

  • Be very careful with applying liquid spot‑on treatments: it is easy to spill some liquid on your hands without realising. Do not touch your pet until the product is dry and be aware that traces of topical parasiticides may continue to transfer to your hands and clothes for days or weeks after application.

  • Consider not using topically applied products (spot-ons or collars) on dogs that swim or are bathed regularly.

  • Do not flush waste medicines, faeces, litter material or cleaning waste from treated pets down the toilet. Ask your vet to put any contaminated packs or empty liquid vials in their waste medicine disposal bins (69).

  • Ask your vets about the environmental risks of the products they recommend and check the labels on any parasite treatments for information about the ecological impact of residues. Try to avoid products that are either known to be hazardous or make no mention of risk.


References 

  1. Böck, K., Polt, R., Schülting, L., 2018. Ecosystem Services in River Landscapes, in: Schmutz, S., Sendzimir, J. (Eds.), Riverine Ecosystem Management: Science for Governing Towards a Sustainable Future, Aquatic Ecology Series. Springer International Publishing, Cham, pp. 413–433.  https://doi.org/10.1007/978-3-319-73250-3_21 

  2. Rose et al. 2015. Contamination of fish in UK fresh water systems: Risk assessment for human consumption. Chemosphere 122, 183–189. https://doi.org/10.1016/j.chemosphere.2014.11.046   

  3. Perkins et al. 2021. Potential role of veterinary flea products in widespread pesticide contamination of English rivers. Sci. Total Environ. 755, 143560. https://doi.org/10.1016/j.scitotenv.2020.143560  

  4. European Commission. Commission implementing regulation (EU) 2018/783 of 29 May 2018 amending implementing regulation (EU) no 540/2011 as regards the conditions of approval of the active substance imidacloprid. Official Journal of the European Union 40–44 (2018). Available at: https://eur-lex.europa.eu/eli/reg_impl/2018/783/oj (Accessed: 17th January 2023) 

  5. European Commission regulation (EU) 2019/1792 of 17 October 2019 amending annexes II, III and V to regulation (EC) no 396/2005 of the European Parliament and of the council as regards maximum residue levels for amitrole, fipronil, flupyrsulfuron-methyl, imazosulfuron, isoproturon, orthosulfamuron and triasulfuron in or on certain products Off. J. Eur. Union, 277(2019).  https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=CELEX:32019R1792&from=EN  (Accessed: 17th January 2023) 

  6. Fera, 2023. PESTICIDES USAGE STATISTICS - Data. URL https://pusstats.fera.co.uk/data/current (accessed 23rd August 2023) 

  7. Environment Agency. Water Quality Monitoring Data GC-MS and LC-MS: Semi- Quantitative. (2022). Available at: https://environment.data.gov.uk/dataset/e85a7a52-7a75-4856-a0b3-8c6e4e303858  (Accessed: 26th September 2022) 

  8. Wells, C., Collins, C.M.T., 2022. A rapid evidence assessment of the potential risk to the environment presented by active ingredients in the UK’s most commonly sold companion animal parasiticides. Environ. Sci. Pollut. Res. 29, 45070–45088. https://doi.org/10.1007/s11356-022-20204-2    

  9. NORMAN Substance Database (2023). Available at:  https://www.norman-network.com/nds/susdat/ (accessed 17th May 2023). 

  10. Bourguet, D., Guillemaud, T., 2016. The Hidden and External Costs of Pesticide Use, in: Lichtfouse, E. (Ed.), Sustainable Agriculture Reviews: Volume 19, Sustainable Agriculture Reviews. Springer International Publishing, Cham, pp. 35–120. https://doi.org/10.1007/978-3-319-26777-7_2  

  11. de Araújo, E.P., Caldas, E.D., Oliveira-Filho, E.C., 2022. Pesticides in surface freshwater: a critical review. Environ. Monit. Assess. 194, 452. https://doi.org/10.1007/s10661-022-10005-y  

  12. Geiger et al. 2010. Persistent negative effects of pesticides on biodiversity and biological control potential on European farmland. Basic Appl. Ecol. 11, 97–105. https://doi.org/10.1016/j.baae.2009.12.001  

  13. Kabasenche, W.P., Skinner, M.K., 2014. DDT, epigenetic harm, and transgenerational environmental justice. Environ. Health 13, 62. https://doi.org/10.1186/1476-069X-13-62  

  14. Grier, J.W., 1982. Ban of DDT and subsequent recovery of reproduction in bald eagles. Science 218, 1232–1235. https://doi.org/10.1126/science.7146905 

  15. Schnoor, J.L., 1981. Fate and transport of dieldrin in Coralville Reservoir: Residues in fish and water following a pesticide ban. Science 211, 840–842. https://doi.org/10.1126/science.211.4484.840  

  16. Snedeker, S.M., 2001. Pesticides and breast cancer risk: a review of DDT, DDE, and dieldrin. Environ. Health Perspect. 109, 35–47. https://doi.org/10.1289/ehp.01109s135  

  17. Aarønes et al. 2021. Within-body distributions and feeding effects of the neonicotinoid insecticide clothianidin in bumblebees (Bombus terrestris). Environ. Toxicol. and Chem. 40, 2781–2790. https://doi.org/10.1002/etc.5154  

  18. Nicodemo et al. 2014. Fipronil and imidacloprid reduce honeybee mitochondrial activity. Environ. Toxicol. and Chem. 33, 2070–2075. https://doi.org/10.1002/etc.2655  

  19. Woodcock et al. 2016. Impacts of neonicotinoid use on long-term population changes in wild bees in England. Nat. Commun. 7, 12459. https://doi.org/10.1038/ncomms12459  

  20. Gibbons, D., Morrissey, C., Mineau, P., 2015. A review of the direct and indirect effects of neonicotinoids and fipronil on vertebrate wildlife. Environ Sci Pollut Res Int 22, 103–118. https://doi.org/10.1007/s11356-014-3180-5  

  21. Floate, K.D et al. 2005. Fecal residues of veterinary parasitides: Nontarget effects in the pasture environment. Ann. Rev. Ent. 50 (1), 153–179. doi:10.1146/annurev.ento.50.071803.130341  

  22. Lappin, M.R., 2018. Update on flea and tick associated diseases of cats. Vet. Parasitol. 254, 26–29. https://doi.org/10.1016/j.vetpar.2018.02.022  

  23. Moriello, K.A., 2003. Zoonotic skin diseases of dogs and cats. Anim. Health Res. Rev. 4, 157–168. https://doi.org/10.1079/ahr200355  

  24. Animal & Plant Health Agency, 2023. Zoonoses and veterinary public health: Quarterly report Q1_January to March 2023. 

  25. Animal & Plant Health Agency, 2023. Zoonoses and Veterinary Public Health: Quarterly report Q2_April to June 2023. 

  26. Animal & Plant Health Agency, 2023. Zoonoses and Veterinary Public Health: Annual report 2022. 

  27. NORD (National Organization for Rare Disorders) - Bartonellosis, 2020. URL https://rarediseases.org/rare-diseases/bartonellosis/ (accessed 2.21.23). 

  28. Skouras et al. 2021. Toxicity, Sublethal and low dose effects of Imidacloprid and Deltamethrin on the Aphidophagous Predator Ceratomegilla undecimnotata (Coleoptera: Coccinellidae). Insects 12, 696. https://doi.org/10.3390/insects12080696  

  29. Franc, M., Beugnet, F., Vermot, S., 2007. Efficacy of fipronil-(S)-methoprene on fleas, flea egg collection, and flea egg development following transplantation of gravid fleas onto treated cats. Vet. Ther. 8, 285–292 

  30. Gaens et al. 2019. Suspected neurological toxicity after oral application of fluralaner (Bravecto®) in a Kooikerhondje dog. BMC Vet. Res. 15, 283. https://doi.org/10.1186/s12917-019-2016-4  

  31. Stanneck et al. 2012. The synergistic action of imidacloprid and flumethrin and their release kinetics from collars applied for ectoparasite control in dogs and cats. Parasit. Vectors 5, 73. https://doi.org/10.1186/1756-3305-5-73  

  32. Sadaria et al. 2017. Passage of fiproles and imidacloprid from urban pest control uses through wastewater treatment plants in northern California, USA. Environ. Toxicol. Chem. 36, 1473–1482. https://doi.org/10.1002/etc.3673  

  33. Webb et al. 2021. Emerging investigator series: Municipal wastewater as a year-round point source of neonicotinoid insecticides that persist in an effluent-dominated stream. Environ. Sci. Process Impacts 23, 678–688. https://doi.org/10.1039/d1em00065a  

  34. Teerlink, J., Hernandez, J., Budd, R., 2017. Fipronil washoff to municipal wastewater from dogs treated with spot-on products. Sci. Total Environ. 599–600, 960–966. https://doi.org/10.1016/j.scitotenv.2017.04.219  

  35. Perkins et al. 2024. Down-the-drain pathways for fipronil and imidacloprid applied as spot-on parasiticides to dogs: Estimating aquatic pollution. Sci Total Environ, 917, e170175. https://doi.org/10.1016/j.scitotenv.2024.170175 

  36. Pisa et al. 2021. An update of the Worldwide Integrated Assessment (WIA) on systemic insecticides. Part 2: impacts on organisms and ecosystems. Environ. Sci. Pollut. Res. 28, 11749–11797. https://doi.org/10.1007/s11356-017-0341-3  

  37. Miller et al. 2020. Common insecticide disrupts aquatic communities: A mesocosm-to-field ecological risk assessment of fipronil and its degradates in U.S. streams. Science Advances 6, eabc1299. https://doi.org/10.1126/sciadv.abc1299  

  38. Alexander, A.C., Culp, J.M., Baird, D.J., Cessna, A.J., 2016. Nutrient–insecticide interactions decouple density-dependent predation pressure in aquatic insects. Freshw. Biol. 61, 2090–2101. https://doi.org/10.1111/fwb.12711  

  39. Pisa et al. 2015. Effects of neonicotinoids and fipronil on non-target invertebrates. Environ. Sci. Pollut. Res. 22, 68–102. https://doi.org/10.1007/s11356-014-3471-x  

  40. Vanni, M.J., 2002. Nutrient Cycling by Animals in Freshwater Ecosystems. Ann. Rev. Ecol. Syst. 33, 341–370. https://doi.org/10.1146/annurev.ecolsys.33.010802.150519  

  41. Dijk, T. C. V., Staalduinen, M. A. V. & Sluijs, J. P. V. der., 2013. Macro-invertebrate decline in surface water polluted with imidacloprid. PLOS ONE 8, e62374. 

  42. Sánchez-Bayo, F., Goka, K. & Hayasaka, D., 2016. Contamination of the aquatic environment with neonicotinoids and its implication for ecosystems. Front. Environ. Sci. 4. https://doi.org/10.3389/fenvs.2016.00071 

  43. Agatz, A., Ashauer, R., Brown, C.D., 2014. Imidacloprid perturbs feeding of Gammarus pulex at environmentally relevant concentrations. Environ. Tox. Chem. 33, 648–653. https://doi.org/10.1002/etc.2480  

  44. Beketov, M.A., Liess, M., 2008. Potential of 11 pesticides to initiate downstream drift of stream macroinvertebrates. Arch. Environ. Contam. Toxicol. 55, 247–253. https://doi.org/10.1007/s00244-007-9104-3  

  45. Mize, S.V., Porter, S.D., Demcheck, D.K., 2008. Influence of fipronil compounds and rice-cultivation land-use intensity on macroinvertebrate communities in streams of southwestern Louisiana, USA. Environ. Pollut. 152, 491–503. https://doi.org/10.1016/j.envpol.2007.03.021  

  46. Overmyer, J.P., Mason, B.N., Armbrust, K.L., 2005. Acute toxicity of Imidacloprid and Fipronil to a nontarget aquatic insect, Simulium vittatum Zetterstedt cytospecies IS-7. Bull. Environ. Contam. Toxicol. 74, 872–879. https://doi.org/10.1007/s00128-005-0662-7  

  47. Roessink et al. 2013. The neonicotinoid Imidacloprid shows high chronic toxicity to mayfly nymphs. Environ. Toxicol. Chem. 32, 1096–1100. https://doi.org/10.1002/etc.2201  

  48. Hejna, M., Kapuścińska, D., Aksmann, A., 2022. Pharmaceuticals in the aquatic environment: A review on eco-toxicology and the remediation potential of algae. Int. J. Environ. Res. Public Health 19, 7717. https://doi.org/10.3390/ijerph19137717  

  49. Toma et al. 2021. New models to predict the acute and chronic toxicities of representative species of the main trophic levels of aquatic environments. Molecules 26, 6983. https://doi.org/10.3390/molecules26226983  

  50. Wollenberger, L., Halling-Sørensen, B., Kusk, K.O., 2000. Acute and chronic toxicity of veterinary antibiotics to Daphnia magna. Chemosphere 40, 723–730. https://doi.org/10.1016/S0045-6535(99)00443-9  

  51. Chagnon et al. 2015. Risks of large-scale use of systemic insecticides to ecosystem functioning and services. Environ. Sci. Pollut. Res. 22, 119–134. https://doi.org/10.1007/s11356-014-3277-x  

  52. Thompson et al. 2016. Gene‐to‐ecosystem impacts of a catastrophic pesticide spill: testing a multilevel bioassessment approach in a river ecosystem. Freshw. Biol., 61, pp.2037-2050. 

  53. Rao, T.R., 2018. Trophic cascades. Reason. 23, 1205–1213. https://doi.org/10.1007/s12045-018-0730-z  

  54. UK Pet Food, 2023. UK Pet Population. URL https://www.ukpetfood.org/information-centre/statistics/uk-pet-population.html (accessed 14th November 2023). 

  55. Bagster, A., Elsheikha, H., 2022. Perception of UK companion animal veterinarians on risk assessment based parasite control. Vet. Parasitol. Reg. Stud. Rep. 34, 100774. https://doi.org/10.1016/j.vprsr.2022.100774  

  56. British Veterinary Association (BVA), 2021 BVA, BSAVA and BVZS policy position on responsible use of parasiticides for cats and dogs. https://www.bva.co.uk/media/4352/bva-bsava-and-bvzs-policy-position-on- responsible-use-of-parasiticides-for-cats-and-dogs.pdf  

  57. Damborg et al. 2016. Bacterial zoonoses transmitted by household pets: State-of-the-art and future perspectives for targeted research and policy actions. J. Comp. Pathol. 155, S27–S40. https://doi.org/10.1016/j.jcpa.2015.03.004  

  58. O’Neill, D.G., Gunn-Moore, D., Sorrell, S., McAuslan, H., Church, D.B., Pegram, C., Brodbelt, D.C., 2023. Commonly diagnosed disorders in domestic cats in the UK and their associations with sex and age. J. Feline Med. Surg. 25, 1098612X231155016. https://doi.org/10.1177/1098612X231155016  

  59. O’Neill, D.G., James, H., Brodbelt, D.C., Church, D.B., Pegram, C., 2021. Prevalence of commonly diagnosed disorders in UK dogs under primary veterinary care: results and applications. BMC Vet. Res. 17, 69. https://doi.org/10.1186/s12917-021-02775-3  

  60. Cooper et al. 2020. Fleas infesting cats and dogs in Great Britain: spatial distribution of infestation risk and its relation to treatment. Med. Vet. Entomol. 34, 452–458.  

  61. Singleton et al. 2017. New approaches to pharmacosurveillance for monitoring prescription frequency, diversity, and co-prescription in a large sentinel network of companion animal veterinary practices in the United Kingdom, 2014–2016. Prev. Vet. Med. 159, 153–161. 

  62. Gupta, R.C., 2007. Fipronil, in: Veterinary Toxicology. Elsevier, pp. 502–504. https://doi.org/10.1016/B978-012370467-2/50140-1  

  63. NOAH, 2023. URL https://www.noahcompendium.co.uk/home (accessed 21st August 2023). 

  64. Horton, H. 2024. Vets urged to cut pesticide flea treatments amid river pollution fears. The Guardian. Available at: https://www.theguardian.com/environment/2024/feb/01/vets-pesticide-flea-treatments-river-pollution-pet-owners-toxic-insecticides-hands#:~:text=Fipronil%20and%20imidacloprid%20are%20widely,of%20pesticides%20known%20as%20neonicotinoids  (accessed 2nd Feb 2024). 

  65. Caneschi et al. 2023. The Use of antibiotics and antimicrobial resistance in veterinary medicine, a complex phenomenon: A narrative review. Antibiotics 12. https://doi.org/10.3390/antibiotics12030487  

  66. Sangster, N., 2001. Managing parasiticide resistance. Vet. Parasitol. 98. https://doi.org/10.1016/s0304-4017(01)00425-3  

  67. Baneth, G., Thamsborg, S.M., Otranto, D., Guillot, J., Blaga, R., Deplazes, P., Solano-Gallego, L., 2016. Major parasitic zoonoses associated with dogs and cats in Europe. J. Comp. Pathol. 155, S54–S74. https://doi.org/10.1016/j.jcpa.2015.10.179  

  68. Sterneberg-van der Maaten, T., Turner, D., Van Tilburg, J., Vaarten, J., 2016. Benefits and risks for people and livestock of keeping companion animals: Searching for a healthy balance. J. Comp. Pathol., 155, S8–S17. https://doi.org/10.1016/j.jcpa.2015.06.007  

  69. Preston-Allen, R., Albini, D., Barron, L., Collins, C., Dumbrell, A., Duncalf-Youngson, H., Jackson, M., Johnson, A., Prentis, A., Spurgeon, D., Stasik, N., Wells, C., Woodward, G., Perkins, R., 2023. Are urban areas hotspots for pollution from pet parasiticides? Imperial College London. https://doi.org/10.25561/102699   


The authors

Hamish Duncalf-Youngson ( Faculty of Natural Sciences, Imperial College London — h.duncalf-youngson21@imperial.ac.uk)

Nicole Stasik (Faculty of Natural Sciences, Imperial College London)

Dr Dania Albini (Department of Biology, University of Oxford)

Dr Leon Barron (Faculty of Medicine, Imperial College London)

Dr CM (Tilly) Collins (Faculty of Natural Sciences, Imperial College London)

Professor Alex Dumbrell (School of Life Sciences, University of Essex)

Dr Michelle Jackson (Department of Biology, University of Oxford)

Professor Andrew Johnson (UK Centre for Ecology and Hydrology, Wallingford)

Dr Rosemary Perkins (School of Life Sciences, University of Sussex)

Dr Andrew Prentis (Grantham Institute, Imperial College London)

Rhys G. G. Preston-Allen (Faculty of Natural Sciences, Imperial College London)

Professor David Spurgeon (UK Centre for Ecology and Hydrology, Wallingford)

Clodagh Wells (Faculty of Life Sciences, University of Bristol)

Professor Guy Woodward (Faculty of Natural Sciences, Imperial College London)


Next
Next

Windermere Info Note