Activity patterns of breeding Hen Harriers Circus cyaneus assessed using nest cameras

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BIRD STUDY, 2017 https://doi.org/10.1080/00063657.2017.1383969 SHORT REPORT Activity patterns of breeding Hen Harriers Circus cyaneus assessed using nest cameras Darío Fernández-Bellon a John O Halloran a, Mark W. Wilson a,b, Sandra Irwin a, Thomas C. Kelly a, Barry O Mahony a and a School of Biological, Earth and Environmental Sciences, University College Cork, Cork, Ireland; b British Trust for Ornithology Scotland, Biological and Environmental Science, University of Stirling, Stirling, UK ABSTRACT Nest camera footage from 13 Hen Harrier Circus cyaneus nests was analysed to document patterns of adult attendance, incubation, brooding and prey delivery rates. Nest attendance was high throughout the incubation stage and began to decrease when chicks were five days old. Chick provisioning increased gradually after hatching and peaked when the chicks were five days old. Daily activity rates were highest during the middle of the day, from 08:00 to 19:00 hours. Hen Harriers Circus cyaneus are listed as an Annex-I species by the European Union Birds Directive (OJEU 2010) and are a species of conservation concern in Ireland and the United Kingdom (Colhoun & Cummins 2013, Eaton et al. 2015). The rarity, declining populations and protected status of this species have led to considerable conservation and monitoring efforts, both as part of national population surveys (Hayhow et al. 2013, Ruddock et al. 2016) and monitoring associated with impact assessment of developments in upland areas. This work is often difficult due to the species secretive nature and low detection rates, with survey protocols recommending multiple watches of between 2.5 and 6 hours duration throughout the season to confirm the presence of breeding pairs (Hardey et al. 2009). Detection of breeding birds and location of nests can be further hindered in certain habitats, such as plantation forest, where birds approaching the nest may remain hidden from view (Hardey et al. 2009). A good understanding of the nesting ecology of the species is crucial for effective monitoring and, ultimately, for its conservation. While a considerable amount of research has been published on different aspects of Hen Harrier breeding success in relation to environmental and anthropogenic factors and its consequences on population trends (Etheridge et al. 1997, Green & Etheridge 1999, Redpath et al. 2002, Amar et al. 2008, Irwin et al. 2011), publications on the behaviour of nesting birds are limited to work carried out in Scotland by direct observations at nest ARTICLE HISTORY Received 11 July 2017 Accepted 29 August 2017 sites (Balfour & Macdonald 1970, Watson 1977, Picozzi 1978, Dickson 1995, Redpath & Thirgood 1997, Amar et al. 2003, Leckie et al. 2008). Remote cameras have been widely used as a tool to monitor different aspects of the ecology of nesting raptors, including diet, nest survival and predation (Smithers et al. 2005, Margalida et al. 2006, Cox et al. 2012). Nest cameras also enable accurate data collection on behavioural patterns of breeding adults which can improve our understanding of nesting ecology and also inform nest finding and population monitoring protocols. Here we present data from nest cameras used at Hen Harrier nests in Ireland, to determine patterns of nest attendance, provisioning rates and activity of breeding birds during different stages of the breeding cycle. We deployed digital trail cameras, under licence, at Hen Harrier nests in the Ballyhoura Mountains, West Clare and Slieve Aughty Mountains (Counties Cork, Clare and Galway in Ireland) during three consecutive breeding seasons (2008 2010). This resulted in recordings from a total of 13 nests which were analysed to quantify behaviours occurring between 05:00 and 22:00 hours. As Hen Harriers are a ground nesting species, the nestlings start to move away from the immediate nest area (and the coverage of nest cameras) when they are just two weeks old. For this reason, only recordings from 10 days prior to hatching and up to 14 days after hatching of the first chick (hereafter hatching ) were included in the analyses. CONTACT Darío Fernández-Bellon dfernandezbellon@ucc.ie; dfernandezbellon@gmail.com School of Biological, Earth and Environmental Sciences, University College Cork, Enterprise Centre, Distillery Fields, North Mall, Cork, Ireland Supplemental data for this article can be accessed https://doi.org/10.1080/00063657.2017.1383969. 2017 British Trust for Ornithology

2 D. FERNÁNDEZ-BELLON ET AL. Nest cameras were activated by motion detection via a passive infra-red sensor. While this technology minimizes the need for regular battery and memory card replacement, it can result in incomplete recordings if certain activities are not detected by the motion sensor. A preliminary assessment of nest camera recordings revealed that gaps of less than 30 minutes in length could be attributed to periods of inactivity with certainty, whereas gaps longer than 30 minutes could reflect periods of inactivity, but could, in a small number of cases include behaviours undetected by the motion sensors. Therefore, we only analysed recordings that included three or more continuous hours of recordings where gaps between sequences were less than 30 minutes long. The proportion of time spent by female Hen Harriers in attendance (on the nest or next to the nest) and time spent actively incubating or brooding (sitting on or covering eggs or chicks) across the day was systematically extracted from the nest camera recordings. Female Hen Harriers are responsible for incubation, brooding and feeding the young, with only anecdotal evidence of the male s involvement in these behaviours (Watson 1977). Female Hen Harriers typically feed away from the nest before the eggs hatch (Hardey et al. 2009), so the timing of prey deliveries to the nest was recorded only after hatching of the first egg. Diurnal patterns and variation in nest attendance, incubation or brooding, and prey deliveries across the nesting period were recorded according to the time of day (05:00 22:00 hours) and stage of the nest in relation to the hatching of the first egg (from day 10 before hatching to day +14). The selection criteria used to exclude non-continuous recordings resulted in a total of 878 hours of recordings analysed from the 13 Hen Harrier nests; all nests were active for the period analysed from day 10 to day 14. Gaps in recordings which resulted in exclusion from analyses can be attributed to the low sensitivity of motion sensor technology currently available in trail cameras. While these criteria ensured the quality of the recordings analysed and provided representative coverage across different times of day and nesting stages, it suggests that nest monitoring of open habitat, ground nesting species would be optimized with continuous recording cameras. Nest attendance was very high, with adult female Hen Harriers remaining in attendance at the nest for at least 90% of the time between 05:00 and 22:00 hours up until seven days after hatching. Attendance progressively decreased thereafter until day 14 after hatching, by which time females were only spending approximately half of their time at the nest (Figure 1 and Table S1 in online supplementary material). Incubation and brooding behaviours followed a similar pattern to nest attendance, with females spending more than 75% of the time incubating or brooding until day 5 after hatching. Brooding then decreased gradually to 22% by day 14 after hatching (Figure 1 and Table S1 in online supplementary material). Coinciding with decreases in brooding and attendance, the nestlings started to move away from the immediate nest cup into the Figure 1. Mean daily rates of total time spent by adult Hen Harriers at the nest (attendance; dashed line), portion of time spent actively incubating or brooding (dotted line) and rates of prey deliveries to nests (continuous black line). Rates are presented by day relative to hatching of the first chick, shaded areas represent ±se.

BIRD STUDY 3 Figure 2. Mean hourly rates of (a) total time spent by adult Hen Harriers at the nest (attendance; dashed line), portion of time spent actively incubating or brooding (dotted line) and (b) rates of prey deliveries to nests (continuous black line). Shaded areas represent ±se. surrounding vegetation more frequently. Across the day, female attendance was most frequent early and late in the day, with lowest nest attendance rates recorded during the middle of the day (Figure 2). A total of 417 prey deliveries were recorded in this study across the 13 nest sites. Prey delivery rates increased gradually after hatching for the first five days. After day 5, delivery rates remained above 0.5 deliveries per hour (ranging from 0.52 to 0.82 deliveries per hour) (Figure 1 and Table S1 in online supplementary material). Deliveries were recorded throughout the day (earliest 05:59, latest 21:41) but rates were generally low before 08:00 and after 19:00, with rates ranging from 0.42 to 0.94 deliveries per hour during the middle of the day (Figure 2 and Table S2 in online supplementary material). It was not possible to discern which of the adults was responsible for hunting, as food passes occurred away from the nest and out of sight of the cameras. However, from day 4 after hatching onwards, males were recorded delivering prey items directly to the nest, never staying there for more than a few seconds. From day 7 after hatching,

4 D. FERNÁNDEZ-BELLON ET AL. these deliveries sometimes took the form of prey drops, where the male overflew the nest and dropped the prey item into the nest without landing. Prey drops accounted for 9.5% of deliveries recorded from day 7 after hatching. The timing of some of the behaviours reported here differs from previous observations at Hen Harrier nests in other regions. We found decreased female attendance as early as seven days after hatching, a pattern usually associated with increased female foraging (Hardey et al. 2009). While our data cannot be used to determine foraging behaviour by the female, it suggests that the decrease in attendance can occur earlier than previously reported (Leckie et al. 2008, Hardey et al. 2009). Daily activity patterns recorded in the current study also deviate from the early morning and late afternoon peaks in activity reported in other parts of the species range (Watson 1977, Hardey et al. 2009). Our findings suggest low levels of activity in the early morning and late evening with higher, but still variable, rates of activity between 08:00 and 19:00. Overall delivery rates recorded in our study were also lower than those reported for nestling periods by other authors who recorded 0.67 1.23 deliveries per hour (Balfour & Macdonald 1970, Watson 1977, Picozzi 1978, Dickson 1995, Redpath & Thirgood 1997). This difference may be due to the fact that our study only covered the initial stages of chick development, when feeding requirements of the young are lower (Dickson 1995). Our results provide new insights into the nesting ecology and behaviours of this threatened species which would require very intensive efforts to assess by traditional fieldwork methods. We highlight temporal variations in attendance behaviours and provisioning rates which can inform conservation management strategies of the species and have implications for survey and monitoring protocols (e.g. potential for disturbance during times of high attendance, timing nest visits to coincide with low attendance periods or optimizing survey times to coincide with activity peaks). These findings also have implications for survey and monitoring protocols. Important increases in activity were recorded at Hen Harrier nests from five days after hatching onwards, suggesting a potential increase in detectability of breeding pairs and nests at this stage. On the other hand, prey drops by male birds, a behaviour which might hinder detection of breeding pairs and location of nests by reducing the occurrence of more obvious food passes, was found to make up nearly 10% of deliveries after day 7. Finally, periods of maximum activity were recorded in the central part of the day, as opposed to early morning and late afternoon activity peaks reported for other parts of the species range and recommended as optimal times for vantage point watches. Further work will be necessary to determine whether these variations in attendance and provisioning rates are specific to the Irish population or add to the variability between nesting pairs recorded elsewhere and whether they relate to nest success or predation. Acknowledgements The authors wish to thank Chris Cullen, Barry O Donoghue, Richard Mills, Geoff Oliver, Paul Troake and Barry Ryan for assistance with fieldwork. Anthony Caravaggi for comments on an earlier version of the manuscript. National Parks & Wildlife Service and Coillte staff and landowners for their involvement and facilitating access to study sites. Funding This research was funded by the Department of Agriculture, Food & the Marine and the National Parks & Wildlife Service. ORCID Darío Fernández-Bellon http://orcid.org/0000-0002-8016-6515 John O Halloran http://orcid.org/0000-0002-8150-7510 References Amar, A., Arroyo, B., Meek, E., Redpath, S. & Riley, H. 2008. Influence of habitat on breeding performance of Hen Harriers Circus cyaneus in Orkney. Ibis 150: 400 404. Amar, A., Redpath, S. & Thirgood, S.J. 2003. Evidence for food limitation in the declining Hen Harrier population on the Orkney Islands, Scotland. Biol. Conserv. 111: 377 384. Balfour, E. & Macdonald, M.A. 1970. Food and feeding behaviour of the Hen Harrier in Orkney. Scot. Birds 6: 57 66. Colhoun, K. & Cummins, S. 2013. Birds of conservation concern in Ireland 2014 2019. Irish Birds 9: 523 544. Cox, W.A., Pruett, M.S., Benson, T.J., Chiavacci, S.J. & Thompson, F.R. 2012. Development of camera technology for monitoring nests. In Ribic, C. A., Thompson III, F. R. & Pietz, P. J. (eds) Video Surveillance of Nesting Birds. Studies in Avian Biology, no. 43: 185 210. University of California Press, Berkeley, CA. Dickson, R.C. 1995. Feeding rates of Hen Harriers in West Galloway. Scot. Birds 18: 104 106. Eaton, M., Aebischer, N., Brown, A., Hearn, R., Lock, L., Musgrove, A., Noble, D., Stroud, D. & Gregory, R. 2015. Birds of conservation concern 4: the population status of birds in the UK, Channel Islands and Isle of Man. Br. Birds 108: 708 746.

BIRD STUDY 5 Etheridge, B., Summers, R.W. & Green, R.E. 1997. The effects of illegal killing and destruction of nests by humans on the population dynamics of the Hen Harrier Circus cyaneus in Scotland. J. Appl. Ecol. 34: 1081 1105. Green, R.E. & Etheridge, B. 1999. Breeding success of the Hen Harrier Circus cyaneus in relation to the distribution of grouse moors and the red fox Vulpes vulpes. J. Appl. Ecol. 36: 472 483. Hardey, J., Crick, H., Wernham, C., Riley, H., Etheridge, B. & Thompson, D. 2009. Raptors: A Field Guide to Survey and Monitoring. The Stationery Office, Edinburgh. Hayhow, D.B., Eaton, M.A., Bladwell, S., Etheridge, B., Ewing, S.R., Ruddock, M., Saunders, R., Sharpe, C., Sim, I.M. & Stevenson, A. 2013. The status of the Hen Harrier, Circus cyaneus, in the UK and Isle of Man in 2010. Bird Study 60: 446 458. Irwin, S., Wilson, M.W., Kelly, T.C., O Mahony, B., Oliver, G., Troake, P., Ryan, B., Cullen, C., O Donoghue, B. & O Halloran, J. 2011. The breeding biology of Hen Harriers Circus cyaneus in Ireland over a five year period. Irish Birds 9: 165 172. Leckie, F.M., Arroyo, B.E., Thirgood, S.J. & Redpath, S.M. 2008. Parental differences in brood provisioning by Hen Harriers Circus cyaneus. Bird Study 55: 209 215. Margalida, A., Ecolan, S., Boudet, J., Bertran, J., Martinez, J.-M. & Heredia, R. 2006. A solar-powered transmitting video camera for monitoring cliff-nesting raptors. J. Field Ornithol. 77: 7 12. OJEU. 2010. EC directive 2009/147/EC of the European Parliament and of the Council of 30 November 2009 on the conservation of wild birds. Official Journal of the European Union L 20: 7 25. Picozzi, N. 1978. Dispersion, breeding and prey of the Hen Harrier Circus Cyaneus in Glen Dye, Kincardineshire. Ibis 120: 498 509. Redpath, S.M. & Thirgood, S.J. 1997. Birds of Prey and Red Grouse. Stationery Office, Cornell University. Redpath, S.M., Thirgood, S.J. & Clarke, R. 2002. Field Vole Microtus agrestis abundance and Hen Harrier Circus cyaneus diet and breeding in Scotland. Ibis 144: E33 E38. Ruddock, M., Mee, A., Lusby, J., Nagle, T., O Neill, S. & O Toole, L. 2016. The 2015 National Survey of Breeding Hen Harrier in Ireland. National Parks and Wildlife Service, Department of the Arts, Heritage and the Gaeltacht, Dublin Smithers, B.L., Boal, C.W. & Andersen, D.A. 2005. Northern Goshawk diet in Minnesota: an analysis using video recording systems. J. Raptor Res. 39: 264. Watson, D. 1977. The Hen Harrier. T&AD Poyser, Berkhamstead.