Background on the Snail Kite in relation to the Apple Snail
The Florida apple snail (Pomacea paludosa) is the nearly-exclusive food of the endangered snail kite (Rostrhamussociabilis plumbeus) in Florida. The kite’s upper mandible is described by Sykes et al. (1995) as slender, deeply hooked, and sharp-tipped, and it is used to cut the snail’s columellar muscle (the only muscle holding the snail to its shell) to remove the edible snail parts from the shell. Snails are captured at the surface down to about 16 cm when snails are engaged in aerial respiration, moving, or resting on vegetation (Sykes et al. 1995).
Snail kites forage in marshes, lake littoral zones, ponds, ephemeral wetlands, and along the shallow banks of rivers and some manmade areas (Sykes et al. 1995). Snail kites are visual hunters, either by aerial course-hunting or perch hunting. Perch hunting involves scanning the water for surfacing snails, from perches 0.15 to 4.6 meters above the water (Sykes et al. 1995). When course-hunting, kites fly 1.5-3 meters above the water surface (Bennetts et al. 1994). When the kite detects a snail, it swoops down to the water surface and extends its feet to take the snail with its talons.
After capturing a snail, kites transport snails in their talons or bill to a perch to feed (Sykes et al. 1995). The kites’ toes are long and slender with curved, long, slender claws described as acute (see above picture - photo by Rob Bennetts). It has been reported that air and water temperatures affect both the number of foraging efforts and capture rates (Cary 1985). Lower capture rates during colder temperatures are likely due to snail inactivity (Hanning 1979). Stevens et al. (2002) quantfied snail inactivity at lower temperatures.
The kite is described as being nonmigratory, but seminomadic in response to factors such as water depth, hydrooperiod, food availability, vegetation growth, nutrient loads, and other habitat changes (Sykes et al. 1995). As noted previously, suitable foraging habitat is characterized by emergent vegetation scattered amongst open-water communities (Bennetts et al. 1994). The emergent vegetation is important for apple snails for egg laying and climbing to the water’s surface to breathe air. Low to moderate stem density areas are important for kite foraging because dense vegetation (e.g., high density cattail and sawgrass) is an impediment to effective foraging (Bennetts et al. 2006).
In addition to areas with too-dense vegetation, snail kites do not forage in areas experiencing a dry down (i.e., no standing water) because snails would be temporarily unavailable (Sykes 1979). However, it should be noted that the movements of kites may also reflect the seminomadic nature of the species—not necessarily foraging conditions (Darby et al. 2006). In other situations when it is thought that kites leave a given wetland due to poor foraging conditions, there may still be snails present—they simply may be present under conditions not amenable to kite foraging. Additionally, as discussed under the “Research” section below, assessments of habitat quality for snail kites and other snail predators should include abundance estimates of snails; Darby et al. (2006) found that little or no use of an area by snail kites does not necessarily reflect a low snail density.
Links to Websites for More Detailed Information on the Snail Kite
This section discusses findings of recent research related to apple snails and snail kites conducted by Philip Darby, Robert Bennetts, and Laksiri Karunaratne.
Habitat Structure and Apple Snail Density: Karunaratne et al. (2006) compared snail densities in two broad habitat types, wet prairie (with emergent macrophytes) and slough (without emergent macrophytes), and explored the effects of structural attributes within wet prairie habitats. They found that: 1) snail densities were greater in prairies than sloughs; 2) within wet prairie habitats, snail densities were higher in Panicum hemitomon -dominated areas than in Eleocharis cellulosa -dominated areas; and 3) lower snail densities were found in dense E. cellulosa compared to less dense E. cellulosa (see Figures 1 and 2 below). These results are significant for water management because continuous inundation of wetlands may convert wet prairie (containing higher snail densities) to lily pad dominated slough habitat (containing lower snail densities).
Figure 1. Snail densities ± SE in slough (gray) and prairie (black) habitats in 7 sites in WCA1 and WCA3A in 2002-03. Adjusted means obtained by dividing mean density by the capture probability (=1.0 in Sites B and C prairie). Figure from Karunaratne et al. (2006).
Figure 2. Snail density estimates ± SE in dense Panicum (black), dense Eleocharis(gray), and sparse Eleocharis (white, dotted), in 5 sites in WCA3A in 2003. Adjusted means obtained by dividing the mean density by the capture probability. Figure from Karunaratne et al. (2006).
Snail Densities and Foraging Kites: For the first time since Florida snail kites were listed as endangered, concurrent reports of snail densities and foraging kites have been made. Darby et al. (2006) reported snail densities and presence/absence data for foraging kites in wet prairies. There was a positive correlation between snail density and the number of foraging kites (Figure 3). Overall, snail density estimates ranged from 0 to 1.8 snails per square meter. The study suggests that snail densities < 0.14 snails per square meter are unlikely to support foraging kites. Darby (pers. comm.) considered this a preliminary indication of what constitutes an adequate prey base for snail kites; nesting kites may require greater snail densities to support foraging by the adults for their nestlings.
Figure 3 from Darby et al. (2006).
Kite Selection of Foraging Habitat: Bennetts et al. (2006) examined foraging habitat selected by snail kites, and quantified the role of snail abundance and vegetation structure in that selection. The researchers found that vegetation structure (dense vs. sparse) was more influential in foraging habitat selection than site, the dominant emergent vegetation species, or abundance of snails. Snail kites captured fewer snails from habitat patches with relatively dense vegetation and high snail densities compared to more open habitat with similar or lower snail densities. It is thought that dense vegetation may limit the kites’ ability to see and/or capture prey (Bourne 1985; Beissinger 1983; Sykes 1987; Bennetts et al. 2006).
Kites Foraging on Non-native Snails: A recent study has also found that the large, non-native channeled apple snail (Pomacea insularum) may present difficulties for foraging snail kites. Darby et al. (2007) found that kites foraging on P. insularum on Lake Tohopekaliga (Osceola County) dropped a greater proportion of the non-native snails compared to the native Florida apple snail (P. paludosa). Prior to reaching a perch to eat, kites dropped 44% of the non-native snail, compared to 0% of the native snails observed in the study (and the 1% reported by another study). Whether or not a non-native was dropped varied considerably between individual kites. The variation in drop rates may reflect kite age/experience differences. The much larger and heavier P. insularum (see picture, P.i. on left, P.p. on right) also took longer to consume, although it would also contain more calories per snail. As suggested in Darby et al. (2007), the size or dimensions of the kites’ claw, and/or the higher weight of P. insularum (37-45% of the weight of a kite), may be the reason for the relatively high drop rate and food handling difficulty.
Literature Cited
Beissinger, S.R. 1983. Hunting behavior, prey selection, and energetics of snail kites in Guyana: consumer choice by a specialist. Auk 100: 84-92.
Bennetts, R.E., M.W. Collopy, J.A. Rodgers, Jr. 1994. The snail kite in the Florida Everglades: A food specialist in a changing environment. Pp 507-532 in Everglades: the ecosystem and its restoration (J. Ogden and S. Davis, eds.). St. Lucie Press, Delray Beach, FL.
Bennetts, R.E., P.C. Darby, and L.B. Karunaratne. 2006. Foraging patch selection by snail kites in response to vegetation structure and prey abundance and availability. Waterbirds 29(1): 88-94.
Bourne, G.R. 1985. The role of profitability in snail kite foraging. Journal Animal Ecology 54: 697-709.
Cary, D.M. 1985. Climatological and environmental factors effecting the foraging behavior and ecology of Everglade Kites. Master’s thesis, Univ. of Miami, Coral Gables, FL, as cited in Sykes et al. (1995).
Darby, P.C., R.E. Bennetts, and L.B. Karunaratne. 2006. Apple snail densities in habitats used by foraging snail kites. Florida Field Naturalist 34(2): 37-47.
Darby, P.C., D.J. Mellow, and M.L. Watford. 2007. Food handling difficulties for snail kites capturing non-native apple snails. Florida Field Naturalist 35(3): 79-85.
Hanning, G.W. 1979. Aspects of reproduction in Pomacea paludosa (Mesogastropoda:Pilidae). M.S. Thesis, Florida State University. Tallahassee. 138 pp.
Karunaratne, L.B., P.C. Darby, and R.E. Bennetts. 2006. The effects of wetland habitat structure on Florida apple snail density. Wetlands 26(4): 1143-1150.
Stevens, A.J., Z.C. Welch, P.C. Darby, and H. F. Percival. 2002. Temperature effects on Florida applesnail activity: implications for snail kite foraging succes and distribution. Wildlife Society Bulletin 30(1): 75-81.
Sykes, P.W. 1987. The feeding habits of the snail kite in Florida, USA. Colonial Waterbirds 10: 84-92.
Sykes, P.W., Jr. 1979. Status of the Everglade Kite in Florida- 1968-1978. Wilson Bulletin 91: 495-511.
Sykes, P.W., Jr., J.A. Rodgers, Jr., and R.E. Bennetts. 1995. Snail kite (Rostrhamus sociabilis). In The Birds of North America, No. 171 (A. Poole and F. Gill, eds.). The Academy of Natural Sciences, Philadelphia, and The American Ornithologists’ Union, Washington, D.C.