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Hunting and Consumption of Passerine Birds by Wild Mallards (Anas Platyrhynchos) Author(S): Silviu O

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Hunting and Consumption of Passerine Birds by Wild Mallards (Anas Platyrhynchos) Author(S): Silviu O Hunting and Consumption of Passerine Birds by Wild Mallards (Anas platyrhynchos) Author(s): Silviu O. Petrovan and Mihai Leu Source: Waterbirds, 40(2):187-190. Published By: The Waterbird Society https://doi.org/10.1675/063.040.0212 URL: http://www.bioone.org/doi/full/10.1675/063.040.0212 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/ page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non- commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Hunting and Consumption of Passerine Birds by Wild Mallards (Anas platyrhynchos) SILVIU O. PETROVAN¹,* AND MIHAI LEU² ¹Department of Zoology, University of Cambridge, The David Attenborough Building, Cambridge, England, CB2 3QZ, U.K. ²Veterinary and Food Safety Authority, Strada Timisoarei, 15, Resita, 320232, Romania *Corresponding author; E-mail: [email protected] Abstract.—Predation of vertebrates by Mallards (Anas platyrhynchos) has rarely been documented and only in relation to fish and amphibians. Mallard foraging behavior was observed at a reservoir bordering Semenic-Caras Gorges National Park in southwest Romania. A group of Mallards comprising one adult female and 10 subadults was recorded hunting, killing and consuming hatching year passerine birds of two species, a Grey Wagtail (Motacilla cinerea) and a Black Redstart (Phoenicuros ochruros). These are the first records of hunting of birds by wild Mallards. This extraordinary new behavior represents substantial diet expansion for this widespread and abundant duck spe- cies. Received 23 February 2017, accepted 4 March 2017. Key words.—Anas platyrhynchos, avian prey, Black Redstart, Grey Wagtail, Mallard, Motacilla cinerea, Phoenicuros ochruros, vertebrate predation. Waterbirds 40(2): 187-190, 2017 The Mallard (Anas platyrhynchos) is one limitation and adverse weather are major fac- of the largest and most abundant and wide- tors for high duckling mortality and why some spread duck species in the world, and also lakes have low abundance or even absence the most hunted waterfowl species in Europe of dabbling ducks (Gunnarson et al. 2004). with around 4.5 million birds shot annually However, even during periods when the re- (Hirschfeld and Heyd 2005). Mallards are quirement for animal protein is at its highest, widely adaptable, from sedentary or dispersive Mallards focus on aquatic invertebrates, and to fully migratory, and they inhabit almost ev- information on vertebrate predation is gener- ery wetland type from natural to man-made, ally rarely reported. We report the first docu- including reservoirs, urban parks and irriga- mented cases of hunting and consumption of tion canals (Carboneras 1992). Due to their birds by wild Mallards. importance as a game species and as the wild relative of the domestic duck, Mallard diet has METHODS been well described. They are regarded as om- nivorous, feeding by dabbling in shallow water The Trei Ape reservoir (45° 12ʹ N, 22° 08ʹ E), border- under 1 m in depth and by grazing on land ing the Semenic-Caras Gorges National Park (Natura 2000 (Snow and Perrins 1998). Their diet primarily ROSCI0226 site) in southwest Romania, was visited over 6 consists of aquatic and terrestrial plants as well days in July 2016. The reservoir, created in 1970, is a large, 53-ha freshwater body at 850-m altitude, with a maximum as various terrestrial and aquatic invertebrates depth around 30 m and a relatively complex structure fol- (Dessborn et al. 2011), but may occasionally lowing river valleys in three main directions. It has moder- include amphibians or fish (Carboneras 1992; ate usage for tourism activities including camping, rowing Olsen et al. 2011). The digestible protein and angling, primarily for European chub (Squalius cepha- content of the food, especially animal pro- lus), European perch (Perca fluviatilis), brown trout (Salmo trutta fario) and Zander (Sander lucioperca). The edges of tein from insect larvae, appears to be a major the reservoir are largely covered by woodland, mostly factor for the survival and growth rate of the deciduous, with beech (Fagus sylvatica) and alder (Alnus ducklings (Street 1978). High-protein food is glutinosa), scrub, and conifers, mainly Norway spruce (Pi- also required by Mallards during egg-laying, cea abies). Sheep (Ovis aries) summer pastures cover the whereas other energy-demanding phases rely higher slopes of the northern shore. Most of the reservoir is deep, open water with little or no aquatic vegetation. on food of plant origin to increase fat deposits However, dense and tall riparian vegetation areas exist (Pehrsson 1984). Experimental work on nutri- where the three main streams feed into the lake, and large ent-poor lakes in Sweden suggested that food populations of amphibians, primarily common frog (Rana 187 188 WATERBIRDS temporaria) and common toad (Bufo bufo), breed in these They were vigorously shaking the riparian sections (Petrovan et al. 2006). Small numbers of Mallards and scrub vegetation on the bank. Follow- (30-50 pairs), Grey Herons ( ) and Moorhen Ardea cinerea ing this activity, the adult Mallard was ob- (Gallinula chloropus) are typically encountered on the water’s edge during March-October, together with more served repeatedly shaking its head laterally occasional observations of species such as Black Stork and compressing a passerine bird in its bill. (Ciconia nigra). During May-September, large numbers of The bird was identified from pictures and summer migrants, especially Black Redstarts (Phoenicuros recording video as a Grey Wagtail fledgling ), Barn Swallows ( ), House Martins ochruros Hirundo rustica with almost complete plumage (Fig. 1). The (Delichon urbicum), and Red-backed Shrikes (Lanius collu- rio), as well as other resident passerine birds such as Black- adult Mallard was repeatedly mobbed by the birds (Turdus merula), breed and raise their young on the vocalizing subadults trying to remove parts edges of the reservoir. The Mallards are not fed by people of the bird carcass, but the adult defended and generally maintain a large flight distance. it. The adult Mallard had obvious difficulties with swallowing the whole bird, partly due to the extended wings of the Grey Wagtail. The RESULTS female Mallard repeatedly submerged the carcass, repositioned it in its bill and tilted A group of Mallards (n = 11) was ob- its head backward, a process lasting over 10 served on 17 July 2016 in the eastern part of min until the Grey Wagtail was eventually en- the lake, in overcast weather with a tempera- tirely consumed. During this time, a second ture of 18 °C, starting at 17:30 hr. The group bird was flushed from the bankside vegeta- consisted of one adult female with 10 sub- tion by the activity of the subadults shaking adults of consistent size, ~2/3 of the adult the long undergrowth, and landed on the size and with incompletely formed plumage. water surface, some 30 m from the bank Using binoculars and telephoto lenses, we and 12 m away from the Mallard group. The observed the Mallards for ~15 min during bird, identified from pictures as a fledgling their foraging activities at the water’s edge. Black Redstart (Fig. 2), opened its wings Figure 1. Adult Mallard defending and consuming a Grey Wagtail. PREDATION OF BIRDS BY MALLARDS 189 Figure 2. (A) Subadult Mallard chasing a juvenile Black Redstart after flushing it from the bank vegetation. Note the very rapid approach by the Mallard. (B) Subadult Mallards attacking and killing the juvenile Black Redstart (bottom). and started thrashing on the water’s surface edge, the first observations of avian hunting giving out distress calls. The Black Redstart and predation by Mallards. The completely was chased by several subadult Mallards and new behavior exhibited by this group is even was repeatedly attacked, grabbed and sub- more significant considering that vertebrate merged as the ducks tried to swallow it or consumption has rarely been described in remove parts of it. Following continuous at- this species and almost only on fish (Carbon- tacks by between two to five Mallards posi- eras 1992; Olsen et al. 2011). Even Pekin (do- tioned in a circle, the Black Redstart disap- mestic) ducks (A. platyrhynchos domesticus) peared, either drowned and submerged or do not exhibit a tendency for aggressive and consumed by one or more of the subadults. predatory behavior in commercial farming During the attack, which lasted less than 3 compared to other species such as Muscovy min, the subadult Mallards continued to vo- Ducks (Cairina moschata) (Riber and Mensh calize in short, repeated calls while trying to 2008). Also, comparing wild and domesticat- take control of the prey. The entire group ed Mallards in an experimental setting dem- of Mallards, including the adult female, then onstrated that wild Mallards show significant emerged onto a floating tree trunk for bask- avoidance and reticence toward novel food ing and preening as the group entered a (Desforges and Wood-Gush 1975), possibly phase of rest. as an indication of either dietary conserva- tism or neophobia. This fits the wider litera- ture observations of avian predators often DISCUSSION avoiding novel insect prey (Coppinger 1969) or reduced predation rates by birds of prey Remarkably for such a widespread and of songbird species with conspicuous plum- well-studied species, these are, to our knowl- age (Götmark 1994).
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