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Ecology of breeding yellow rails at Seney National Wildlife Refuge /Stenzel, Jeffrey R. January 1982 (has links)
Thesis (M.S.)--Ohio State University. / Includes bibliographical references (leaves 94-96). Available online via OhioLINK's ETD Center
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The biology, ecology and conservation of four Flufftail species, Sarothrura (Aves: Rallidae)Taylor, Peter Barry. January 1994 (has links)
The distribution, status, biology and ecology of four flufftail species were investigated in South Africa and Zimbabwe. The Redchested Flufftail is a successful and widely distributed species, occupying a wide range of dense vegetation, from seasonally wet grassland and sedges to permanently
shallowly flooded reedbeds. It colonizes artificially created wetland patches and occupies very small patches of suitable habitat. Redchested Flufftails maintain a permanent pair bond and are permanently territorial and entirely sedentary. Their habitat is relatively stable but unpredictable catastrophic events such as burning may force temporary emigration in winter or spring. Displaced birds move a short distance, occupy often marginally suitable habitat and recolonize burned areas as soon as vegetation cover becomes adequate. Periodic burning improves habitat quality, and recommendations are formulated for the management of wetland habitats by burning. The size of the winter territory is larger than the minimum required for survival and provides an insurance against forced emigration, while immatures often share parental territories in winter. The Striped Flufftail's grassland habitats in Natal are decreasing and its numbers are declining. Striped Flufftails are sedentary in low-altitude grassland habitats, but in high-altitude sourveld the decrease in invertebrate food forces emigration in April-June, when the birds move to
unknown wintering destinations (movements are possibly altitudinal). Return time to unburned vegetation is dependent upon invertebrate food availability. Return time to burned vegetation is governed by the development of suitable cover, which may occur too late in the breeding season to permit occupation. The species is well adapted to frequent burning of its habitats, which serves to maintain suitable fire-climax grassland, but is also adapted to post-fire-climax vegetation types. The Whitewinged Flufftail is rare but its occurrence was regularly noted during the summer at four sites in Natal and the Transvaal. Habitat preferences and movement patterns were clarified, as was the bird's ecological segregation from the Redchested Flufftail. No conclusive evidence was
found for breeding in South Africa and it is suggested that lack of suitable breeding habitat (possibly as a result of its being occupied by breeding Redchested Flufftails) may account for this. Some aspects of the bird's behaviour and calling were investigated. In view of this bird's threatened status and the continuing destruction of its wetland habitats, further surveys are urgently required to clarify the bird's status and the full extent of suitable habitat in South Africa, while a captive breeding programme is recommended to study breeding behaviour. The Buffspotted Flufftail inhabits a wide variety of forested and bushed habitats, and in Natal is a successful colonist of exotic vegetation in gardens. Its breeding biology, territorial and aggressive behaviour, and feeding ecology, were investigated in detail. It has regular seasonal movements in Natal, probably both altitudinal and coastal, although birds may remain throughout the year in areas where conditions are suitable. Seasonal departures are correlated with decreasing invertebrate food availability, while return time is largely governed by food availability, although cover development in exotic vegetation delayed recolonization at one site. The pair bond and the territory are maintained throughout the breeding season, and possibly throughout the year under suitable conditions. Adult
mortality is probably high and the species' breeding strategy emphasises fecundity, this being achieved by a large clutch size, a very restricted period of parental care and rapid re-nesting. Juvenile mortality is high. The plumage, behavioural and vocal development of the young were studied in detail. / Thesis (Ph.D.)-University of Natal, Pietermaritzburg, 1994.
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The status and distribution of rails and other marsh birds in natural and restored wetlands in northern IndianaWeiss, Ronald A. January 1995 (has links)
This study examines the status and distribution of rail populations in northern Indiana. Because rails are secretive and difficult to study, there have been few attempts in Indiana to determine the impact of wetland loss on the populations of rails and other marsh-nesting birds. There can be little doubt, however, that the loss of Indiana wetlands during historic times has caused a dramatic decline in rail populations.Using tape-recorded calls to elicit vocalizations, the status and distribution of five species of rails were studied in a 25,900 km2 area in northern Indiana in 1993 and 1994. A total of 107 surveys were conducted at 46 natural wetlands and 42 restored wetlands. The species surveyed were Sora (Porzana carolina), Virginia Rail (Rallus limicola), King Rail (Rallus elegans), Yellow Rail (Coturnicops noveboracensis), and Black Rail (Laterallus jamaicensis). Playbacks were also used to detect American Bittern (Botaurus lentiginosus), Least Bittern (Ixobrychus exilis), Marsh Wren (Cistothorus palustris) and Sedge Wren (Cistothorus platensis). Data were also collected on all other species of marsh-nesting birds detected during this study.Rails exhibited a patchy distribution. A total of 25 Soras, 33 Virginia Rails, and 1 King Rail was detected in natural wetlands in 1993. In 1994, 75 Soras, 46 Virginia Rails, and 1 King Rail was detected in the natural wetlands. A total of 30 Soras and 9 Virginia Rails was found in the restored wetlands studied in 1993 and 1994. No Yellow or Black Rails were found. Ten Least Bitterns, 31 Marsh Wrens, and 6 Sedge Wrens were detected in natural wetlands, but these species were not observed in restored wetlands.The occurrence of rails in natural wetlands was positively correlated with wetland size, presence of shrub vegetation in the watershed, amount of emergent vegetation, proximity of other wetlands, and extent of cattail cover. Negative correlations were found for human disturbance, amount of open water, and watershed characteristics. The strongest negative correlationswere found for human disturbances in or around the wetland.In restored wetlands, a significant difference was found between the occurrence of Sora and Virginia Rails with Soras occurring more frequently than Virginia Rails. A near significant difference in rail occurrence between natural and restored wetlands was also found, with rails occurring more frequently in natural wetlands, suggesting that natural wetlands surveyed may be a more suitable habitat for rails than the restored wetlands surveyed.Restored wetlands surveyed in this study failed to attract American Bitterns, Least Bitterns, Marsh Wrens or Sedge Wrens. American Bitterns were reported in natural wetlands during this study, but they were not observed. / Department of Biology
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