As small birds with rounded wings and strong legs, antbirds have mostly sombre grey, white, brown and rufous plumage. For the most part they are sexually dimorphic in pattern and colouring. Some species communicate warnings to each other by exposing white feather patches on their backs or shoulders. Most have heavy bills, which in many species are hooked at the end.
Most species live in forests, although a few are found in other habitats. Insects and other arthropods form the most important part of their diet, although small vertebrates are occasionally taken. Most species feed in the understory and midstory of the forest, although a few feed in the canopy and a few on the ground. Many join mixed-species feeding flocks, and a few species are core members. To various degrees, around eighteen species specialise in following columns of army ants to eat the small invertebrates flushed by the ants, and many others may feed in this way opportunistically.
Antbirds are monogamous, mate for life and defend territories. They usually lay two eggs in a nest that is either suspended from branches or supported on a branch, stump or mound on the ground. Both parents share the tasks of incubation and of brooding and feeding the nestlings. After fledging, each parent cares exclusively for one chick.
Thirty-eight species are threatened with extinction due to human activities. Antbirds are not targeted by either hunters or the pet trade. The principal threat is habitat loss, which causes habitat fragmentation and increased nest predation in habitat fragments.
Although the taxonomic layout of the Thamnophilidae is based on studies from the mid-19th century, when fewer than half the present species were known, comparison of the myoglobin intron 2, GAPDH intron 11 and the mtDNA cytochrome b DNA sequences has largely confirmed it. There are two major clades – most antshrikes and other larger, strong-billed species as well as Herpsilochmus, versus the classical antwrens and other more slender, longer-billed species – and the monophyly of most genera was confirmed.
The Thamnophilidae contains several large or very large genera, and a considerable number of small or monotypic ones. Several of these, which have always been difficult to assign, seem to form a third, hitherto unrecognised clade independently derived from ancestral antbirds. The results also confirmed suspicions of previous researchers that some species, most notably in Myrmotherula and Myrmeciza, need to be assigned to different genera. Still, due to the difficulties of sampling from such a large number of often poorly known species, the assignment of some genera is still awaiting confirmation.
The antbirds are a group of small to medium-sized passerines that range in size from the large Giant Antshrike, which measures 45 cm (18 in) and weighs 150 g (5.29 oz), to the tiny 8-cm (3 in) Pygmy Antwren, which weighs 7 g (0.25 oz). In general, they have short rounded wings that provide good manoeuvrability when flying in dense undergrowth. The legs are large and strong, particularly in species that are obligate ant-followers. These species are adapted to gripping vertical stems and saplings, which are more common than horizontal branches in the undergrowth, and thus the ability to grip them is an advantage for birds following swarms of army ants. The claws of these species are longer than those of species that do not follow ants, and the soles of some species have projections that are tough and gripping when the foot is clenched. Tarsus length in antbirds is related to foraging strategy. Longer tarsi typically occur in genera such as the Thamnophilus antshrikes that forage by perch-gleaning (sitting and leaning forward to snatch insects from the branch), whereas shorter tarsi typically occur in those that catch prey on the wing, such as the Thamnomanes antshrikes.
Most antbirds have proportionately large, heavy bills. Several genera of antshrike have a strongly hooked end to the bill, and all antbirds have a notch or 'tooth' at the end of the bill which helps in holding and crushing insect prey. The two genera of bushbirds have upturned chisel-like bills.
The plumage of antbirds is soft and not brightly coloured, although it is occasionally striking. The colour palette of most species is blackish shades, whitish shades, rufous, chestnut and brown. Plumages can be uniform in colour or patterned with barring or spots. Sexual dimorphism – differences in plumage colour and pattern between males and females – is common in the family. Overall the pattern within the family is for the males to have combinations of grey, black or or white plumage and the females having buff, rufous and brown colours. For example, the male Dot-winged Antwren is primarily blackish, whereas the female has rust-coloured underparts. In some genera, such as Myrmotherula, species are better distinguished by female plumage than by male. Many species of antbirds have a contrasting 'patch' of white (sometimes other colours) feathers on the back (known as a interscapular patches), shoulder or underwing. This is usually concealed by the darker feathers on the back but when the bird is excited or alarmed these feathers can be raised to flash the white patch. Dot-winged Antwrens puff out white back patches, whereas in Bluish-slate Antshrikes and White-flanked Antwrens the white patch is on the shoulder.
The distribution of the antbirds is entirely Neotropical, with the vast majority of the species being found in the tropics. A few species reach southern Mexico and northern Argentina. Some species, such as the Barred Antshrike, have a continental distribution that spans most of the South and Middle American distribution of the family; others, such as the Ash-throated Antwren, have a tiny distribution.
Antbirds are mostly birds of humid lowland rainforests. Few species are found at higher elevations, with less than 10% of species having ranges above 2000 m (6500 ft) and almost none with ranges above 3000 m (10000 ft). The highest species diversity is found in the Amazon Basin, with up to 45 species being found in single locations in sites across Brazil, Colombia, Bolivia and Peru. The number of species drops dramatically towards the further reaches of the family's range; there are only seven species in Mexico, for example. Areas of lower thamnophilid diversity may contain localised endemics, however. The Yapacana Antbird, for example, is restricted to the stunted woodlands that grow in areas of nutrient-poor white-sand soil (the so-called Amazonian caatinga) in Brazil, Venezuela and Colombia. Some species are predominantly associated with certain microhabitats within a greater ecosystem; for example, the Bamboo Antshrike is predominantly found in bamboo patches.
The main component of the diet of all antbirds is arthropods. These are mostly insects, including grasshoppers and crickets, cockroaches, praying mantises, stick insects and the larvae of butterflies and moths. In addition antbirds often take spiders, scorpions and centipedes. They swallow smaller prey items quickly, whereas they often beat larger items against branches in order to remove wings and spines. Larger species can kill and consume frogs and lizards as well, but generally these do not form an important part of the diet of this family. In addition other food items may be eaten, including fruit, eggs and slugs.
The family uses a number of techniques to obtain prey. The majority of antbirds are arboreal, with most of those feeding in the understory, many in the middle story and some in the canopy. A few species feed in the leaf litter; for example the Wing-banded Antbird forages in areas of dense leaf-litter. It does not use its feet to scratch the leaf litter, as do some other birds; instead it uses its long bill to turn over leaves rapidly (never picking them up). The antbirds that forage arboreally show a number of techniques and specialisations. Some species perch-glean, perching on a branch watching for prey and snatching it by reaching forward, where others sally from a perch and snatch prey on the wing. In both cases birds will hop through the foliage or undergrowth and pause, scanning for prey, before pouncing or moving on. The time paused varies, although smaller species tend to be more active and pause for shorter times.
Many species of antbirds participate in mixed-species feeding flocks, forming a large percentage of the participating species within their range. Some of these are core or "nuclear species". These nuclear species share territories with other nuclear species but exclude conspecifics (members of the same species) and are found in almost all flocks; these are joined by "attendant species". Loud and distinctive calls and conspicuous plumage are important attributes of nuclear species as they promote cohesion in the flock. The composition of these flocks varies geographically; in Amazonia species of Thamnomanes antshrike are the leading nuclear species; elsewhere other species, such as the Dot-winged Antwrens and Checker-throated Antwrens, fill this role. Other species of antwren and antbird join them along with woodcreepers, ant-tanagers, foliage-gleaners and greenlets. The benefits of the mixed flock are thought to be related to predation, since many eyes are better for spotting predatory hawks and falcons. Comparisons between multi-species feeding flocks in different parts of the world found that instances of flocking were positively correlated with predation risk by raptors. For example, where Thamnomanes antshrikes lead the group they give loud warning calls in the presence of predators. These calls are understood and reacted to by all the other species in the flock. The advantage to the Thamnomanes antshrikes is in allowing the rest of the flock, which are typically gleaners, to act as beaters, flushing prey while foraging which the antshrikes can obtain by sallying. Similar roles are filled in other flocks by other antbird species or other bird families, for example the shrike-tanagers. Within the feeding flocks competition is reduced by microniche partitioning; where Dot-winged Antwrens, Checker-throated Antwrens and White-flanked Antwrens feed in flocks together, the Dot-wings feed in the densest vines, the White-flank in less dense vegetation, and the Checker-throats in the same density as the latter but in dead foliage only.
Swarms of army ants are an important resource used by some species of antbird, and the one from which the family's common name is derived. Many species of tropical ant form large raiding swarms, but the swarms are often nocturnal or raid underground. While birds visit these swarms when they occur, the species most commonly attended by birds is the Neotropical species Eciton burchellii, which is both diurnal and surface-raiding. It was once thought that attending birds were actually eating the ants, but numerous studies in various parts of E. burchellii's range has shown that the ants act as beaters, flushing insects, other arthropods and small vertebrates into the waiting flocks of "ant-followers". The improvement in foraging efficiency can be dramatic; a study of Spotted Antbirds found that they made attempts at prey every 111.8 seconds away from ants, but at swarms they made attempts every 32.3 seconds. While many species of antbirds (and other families) may opportunistically feed at army ant swarms, 18 species of antbird are obligate ant-followers, obtaining most of their diet from swarms. With only three exceptions these species never regularly forage away from ant swarms. A further four species regularly attend swarms but are as often seen away from them. Obligate ant-followers visit the nesting bivouacs of army ants in the morning to check for raiding activities; other species do not. These species tend to arrive at swarms first, and their calls are used by other species to locate swarming ants.
Because army ants are unpredictable in their movements, it is impracticable for obligate ant-followers to maintain a territory that always contains swarms to feed around. Antbirds have evolved a more complicated system than the strict territoriality of most other birds. They generally (details vary among species) maintain breeding territories but travel outside those territories in order to feed at swarms. Several pairs of the same species may attend a swarm, with the dominant pair at the swarm being the pair which holds the territory that the swarm is in. In addition to competition within species, competition among species exists, and larger species are dominant. In its range, the Ocellated Antbird is the largest of the obligate ant-following antbirds and is dominant over other members of the family, although it is subordinate to various species from other families (including certain woodcreepers, motmots and the Rufous-vented Ground-cuckoo). At a swarm the dominant species occupies positions above the central front of the swarm, which yields the largest amount of prey. Smaller, less dominant species locate themselves further away from the centre, or higher above the location of the dominant species, where prey is less plentiful.
What is known about the nests and breeding biology of antbirds is based on the species that have been studied and whose nests have been located. Even in relatively well-known species the breeding behaviour can be poorly known; for example the nest of the Ocellated Antbird was first described in 2004. Nests are constructed by both parents, although the male undertakes more of the work in some species. Antbird nests are cups of vegetation such as twigs, dead leaves and plant filaments, and they follow two basic patterns: either suspended or supported. Suspended cups, which may hang from forks in branches, or between two branches, are the more common style of nest. Supported nests rest upon branches, amongst vines, in hollows, and sometimes on mounds of vegetation on the ground. Each species nests at the level where it forages, so a midstory species would build its nest in the midstory. Closely related species nest in the same ways. For example antvireos in the genus Dysithamnus are all suspension nesters.
Almost all antbirds lay two eggs. A few species of antshrike lay three eggs, and a smaller number of antbirds lay one egg, but this is unusual. Small clutch sizes are typical of tropical birds compared to more temperate species of the same size, possibly due to nest predation, although this is disputed. Both parents participate in incubation, although only the female incubates at night. The length of time taken for chicks to hatch is 14–16 days in most species, although some, such as the Dusky Antbird, can take as long as 20 days. The altricial chicks are born naked and blind. Both parents brood the young until they are able to thermoregulate, although, as with incubation, only the female broods at night. In common with many songbirds, the parents take faecal sacs for disposal away from the nest. Both parents feed the chicks, often bringing large prey items. When the chicks reach fledging age, after 8–15 days, attending parents call their chicks. As each chick leaves the nest it is cared for exclusively from then on by the parent that was present then. After the first chick fledges and leaves with a parent the remaining parent may increase the supply of food to speed up the process of fledging. After fledging, chicks spend the first few days well hidden as the parents bring them food. Chicks of some species may not become independent of the parents for as long as four months in some antwrens, but two months is more typical for the rest of the family.
It was once suggested that the relationship between the obligate and regular ant-followers and the army ants, particularly Eciton burchellii, was mutualistic, with the ants benefiting by having the birds chase prey back down towards them. However experiments where ant-followers were excluded have shown that the foraging success of the army ants was 30% lower when the birds were present, suggesting that the birds' relationship was in fact parasitic. This has resulted in a number of behaviours by the ants in order to reduce kleptoparasitism, including hiding of secured prey in the leaf litter and caching of food on trails. It has been suggested that the depressive effect of this parasitism slows the development of E. burchellii swarms and in turn benefits other ant species which are preyed upon by army ants. The ant-following antbirds are themselves followed by three species of butterfly in the family Ithomiinae which feed on their droppings. Bird droppings are usually an unpredictable resource in a rainforest, but the regular behaviour of ant-followers makes the exploitation of this resource possible.
As of April 2008, 38 species are considered by the IUCN to be near threatened or worse and therefore at risk of extinction. Antbirds are neither targeted by the pet trade nor large enough to be hunted; the principal cause of the decline in antbird species is habitat loss. The destruction or modification of forests has several effects on different species of antbirds. The fragmentation of forests into smaller patches affects species that are averse to crossing gaps as small as roads. If these species become locally extinct in a fragment, this reluctance to cross unforested barriers makes their re-establishment unlikely. Smaller forest fragments are unable to sustain mixed-species feeding flocks, leading to local extinctions. Another risk faced by antbirds in fragmented habitat is increased nest predation. An unplanned experiment in fragmentation occurred on Barro Colorado Island, a former hill in Panama that became an isolated island during the flooding caused by the creation of the Panama Canal. Numerous species of antbird formerly resident in the area were extirpated, in no small part due to increased levels of nest predation on the island. While the species lost from Barro Colorado are not globally threatened, they illustrate the vulnerability of species in fragmented habitats and help explain the declines of some species. The majority of threatened species have very small natural ranges. Some are also extremely poorly known; for example the Rio de Janeiro Antwren is known only from a single specimen collected in 1982, although there have been unconfirmed reports since 1994 and it is currently listed as critically endangered. Additionally, new species are discovered at regular intervals; the Caatinga Antwren was described in 2000, the Acre Antshrike in 2004, the Sincorá Antwren in 2007, and the description of a relative of the Paraná Antwren discovered in 2005 in the outskirts of São Paulo is being prepared. While not yet scientifically described, conservation efforts have already been necessary, as the site of discovery was set out to be flooded to form a reservoir. Consequently, 72 individuals were captured and transferred to another locality.
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