The nests of tree swifts are tiny cups, barely large enough to hold the single egg. They are placed on small limbs, high up in trees, where they are subject to being moved about by the wind. The egg is glued to the bottom of the nest with the sticky saliva of the parent; this prevents the egg from being turned during incubation (as is done by virtually all other birds). It is thought that the waving of the nest branch in the wind may in some way act as a substitute to turning the egg, moving the egg’s contents within the shell. One of the true swifts, the palm swift (Cypsiurus parvus) of the Old World tropics, also glues its egg into the nest, but the nest is very different. This species utilizes feathers and plant material and attaches the nest, little more than a flat pad, to the underside of a hanging palm leaf, where it, too, is subject to agitation by the wind.

For such a relatively uniform group in a structural sense, the true swifts show a surprising variation in nesting habits. The New World palm swifts (Tachornis), like those of the Old World, place their nests under palm leaves, but the nest itself is more elaborate, being a sack entered from below through a tubular tunnel. Most other swifts nest either inside a crevice or hole (such as in the ground, in a tree, or between rocks), where they build a shallow cup of feathers and plant material as a flooring, or inside hollow trees, caves, or such man-made structures as buildings, wells, and tunnels. The nests may be circular cups placed on ledges or semicircular brackets attached to the walls. The bracket nests are fastened to vertical surfaces with a sticky secretion from the large salivary glands; in the swiftlet genus Collocalia, this substance may comprise most or all of the nest material itself. One species, the white-naped swift of Mexico, builds no nest at all but lays its eggs in a depression on bare sand on ledges deep inside caves.

Clutches in the true swifts vary from one to about six white eggs, with the higher numbers being found among some of the more northern species of the genera Chaetura and Aeronautes. Incubation is by both sexes. The young are hatched completely naked. Young swifts are left unattended for longer periods than is true of most altricial (helpless) nestlings; the adults spend a substantial amount of time foraging for the relatively small insects on which they feed, in order to capture a sufficient number to warrant a trip back to the nest. In bad weather, when few insects are flying, the young may be left unbrooded for hours. In some birds this would normally lead to chilling and perhaps death, but young swifts maintain an essentially poikilothermic (cold-blooded) condition for the first few weeks of life, the body temperature dropping to near that of the environment without harming the young bird. In one genus, Cypseloides, the young develop a coat of downlike semiplumes (fluffy feathers) prior to the appearance of the juvenile pennaceous (smooth) contour feathers, and this fluffy coat also appears to aid in thermoregulation.

Many species of swifts are colonial nesters, and even those that are relatively solitary during the breeding season appear to be highly gregarious at other times of year. Night roosts of some species may number hundreds of individuals, and foraging flocks may include several species. The northernmost species, such as the European swift and the chimney swift, are long-distance migrants. The winter home of the latter species was a mystery for many years until 1944; Indians in the upper Amazonian forests of Peru were found to have in their possession numbered aluminum bands that had been placed on the legs of chimney swifts by the United States Bureau of Biological Survey. Migration is also known to occur in some of the tropical species, notably in Africa.

India’s population of the house swift has two breeding seasons per year. It is one of the few birds in the world in which this phenomenon has been demonstrated. Adult males are in full breeding condition in late January and again in May and June; eggs are laid in January and February and again in June to September. The molt cycle, however, appears to be independent of the breeding cycle, and the flight feathers are renewed only once a year.

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Unlike swifts, hummingbirds are largely polygamous. Female hummingbirds are the primary nest builders, and, although males may build nests as well, they are not used by the females. Most hummingbird nests, saddled on a branch, are composed of fine vegetable fibres, spider webs, fragments of bark, and lichens. Among the most interesting exceptions are the nests constructed by the hermits. They are long, slender, woven baskets of plant fibres and down, suspended from a strip of vegetation attached at only one side of the nest. The weight of the incubating female and, later, the weight of the young is counterbalanced by pebbles or clods of hard earth at the bottom of the dangling nest. The usual hummingbird clutch is two white eggs, and the female alone incubates and cares for the young in most species, although this is difficult to determine in the species that are not sexually dimorphic. In the sexually dimorphic species the juveniles usually resemble the adult females, although some genera have a distinctive juvenile plumage that resembles neither parent. The parent feeds the young by thrusting its bill deep within the young bird’s throat and regurgitating food.

Like the northern swifts, the hummingbirds that breed farthest north are the most highly migratory. The ruby-throated hummingbird was known to make annual nonstop flights across the Gulf of Mexico long before physiologists understood avian metabolism well enough to determine how this could be possible for such a tiny bird. Migration takes place among some Southern Hemisphere hummingbirds, such as the giant hummingbird and the green-backed fire crown (Sephanoides sephanoides); the latter reaches Tierra del Fuego and is thus the southernmost hummingbird, but there is little information about the nature and extent of these movements.