- Yellow-billed Teal
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Yellow-billed Teal Anas flavirostris Scientific name definitions

Carles Carboneras and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated April 19, 2016

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Introduction

The Yellow-billed Teal is a common duck of southern South America.  The species shows the compact proportions typical of teal and is gray below and brown above with a dark brown head and yellow bill.  Overall Yellow-billed Teal look like a darker, smaller and less elegant version of the widely sympatric Yellow-billed Pintail.  Birds from the high altiplano are pale silvery below, whereas the lowland race is darker grayish brown.  In flight and when excited, males give a creaky "peeet" call and females quack, also typical of teal.

Field Identification

35–45 cm; 388–830 g (1). Head sometimes paler than in bird depicted. Both races resemble <em>A. georgica</em> , but always smaller, shorter-necked and darker-headed  . Male lacks eclipse plumage, has head and neck pale grey to buff, heavily spotted or vermiculated black, upperparts black and brownish, belly and sides grey to pale brown, spotted  darker on breast, uppertail-coverts and tail grey-brown, wings grey-brown on coverts, becoming darker on remiges, speculum  velvet black and metallic green, bordered in front by rufescent band and buff or white on trailing edge; bill yellow with black culmen and tip and pale grey to cream-coloured mandible, legs  and feet grey, and eyes brown. Female slightly smaller and duller, with scallops  (rather than spots) on breast and sides, and bill paler (at least in nominate) with brown culmen stripe (2). Juvenile with duller yellow bill and spotting on underparts, while upperparts appear obscurely mottled. Subspecies vary in colour: <em>oxyptera</em> has dark markings limited to sides of breast, pale parts seem white from a distance, contrasting with dark head , and has slender dull yellow bill  .

Systematics History

Editor's Note: This article requires further editing work to merge existing content into the appropriate Subspecies sections. Please bear with us while this update takes place.

Sometimes placed in genus Nettion. Usually united with A. andium in one species, but separation accepted here (see that species). Form oxyptera differs from nominate flavirostris in its lightly vs heavily mottled breast, mantle and back and greyish-cream vs dingy grey-brown underparts (2), and its slightly larger size apparently best expressed by longer wing (1 or 2). Two subspecies recognized.

Subspecies


EBIRD GROUP (MONOTYPIC)

Yellow-billed Teal (flavirostris) Anas flavirostris flavirostris Scientific name definitions

Distribution

N Argentina, Uruguay and SE Brazil S to Tierra del Fuego; Falkland Is, South Georgia.

EBIRD GROUP (MONOTYPIC)

Yellow-billed Teal (oxyptera) Anas flavirostris oxyptera Scientific name definitions

Distribution

Andes from C Peru (Cajamarca) S to NW Argentina (Catamarca).

Distribution

Editor's Note: Additional distribution information for this taxon can be found in the 'Subspecies' article above. In the future we will develop a range-wide distribution article.

Habitat

Variety of freshwater lakes , rivers and marshes, generally at high altitude in mountainous country in bogs with ponds and creeks, but also in lower ground. In winter, commonly on coast. Race oxyptera principally occurs at 2500–4500 m (1).

Movement

Southernmost breeding birds winter in more temperate regions, as far N as Uruguay, Paraguay and SE Brazil  (Santa Catarina  , Aug 1988, Feb 199, Mar 1992 and several records in Mar 2003–Jan 2005, and Rio de Janeiro, Sept 1990) (3, 4, 5). Falkland Is and Andean populations mainly sedentary, the latter perhaps forced to descend to lower altitudes by adverse winter weather, e.g. reaching of Pacific lowlands of N Chile (Lluta Valley) and S Peru (Huasco Valley) (1). Has been recorded up to c. 90 km offshore from Patagonia in Sept (6).

Diet and Foraging

Small aquatic invertebrates (insects, crustaceans, amphipods) and seeds, fruits and vegetative parts of aquatic plants (seaweed, algae). In Chile, in winter, stomach contents (race flavirostris) comprised 79% Potentilla anserina and 6·4% Trifolium, or 72·6% P. anserina and 5·9% Ranunculus by dry weight, while in summer stomachs of both young and adults contained cladocerans (Bosmina), midge larvae, insects, fish eggs, amphipods and seeds (1). Filters mud while walking along water's edge, or gathers food items by dabbling, head dipping or upending in shallow waters, and very occasionally diving (1).

Sounds and Vocal Behavior

Male gives loud, single-syllabled “krick” in display, alarm and when separated when female, as well as a similar whistled note in other displays, various chittering notes and soft, meow-like calls when agitated; female utters loud quack note in alarm, when separated from male or brood, and encourages male to mate with grating “rraak” and “Decrescendo” call has 5–12 syllables (1).

Breeding

Season variable according to locality; season generally Oct–Mar in race oxyptera (with perhaps additional clutches in Jun–Jul in Peru for oxyptera) and Aug–Jan in nominate race (1). Monogamous with long-term pair-bonds (lasting up to six years), although extra-pair courtship is frequently observed in nominate race (7). In single pairs or loose groups, e.g. when using old parakeet cavities; nest typically well hidden, often among thick vegetation or in trees, near water, but also in cavities in banks or rocky outcrops (race oxyptera) or old ground burrows belonging to woodpeckers (probably Campo Flickers Colaptes campestris) or abandoned chambers of Monk Parakeet  (Myiopsitta monachus) (8, 7), typically 5–20 m above ground in Celtis tala or Eucalyptus, and other tree nest-sites (race flavirostris) (1), including once in Nothofagus in S Chile, where species might compete with Slender-billed Parakeets (Enicognathus leptorhynchus) for suitable cavities (9). In areas where ducks commonly use Myiopsitta monachus nests, inter- and intraspecific competition is intense, with parakeets aggressively defending occupied cavities, forcing teal to compete with each other for abandoned cavities, thus male teals assist their mates to obtain and defend sites against other pairs (7); teal sometimes attempt to nest in nest chambers already occupied by parakeets (10). High nest-site fidelity (63% in female and 56·3% in male) (1), and in Buenos Aires province, Argentina, 19 of 22 females returned to same nest-site in subsequent season (7). Clutch 5–13 dark cream eggs (once 18, involving two females laying in same cavity) (1), laid at 1–2·4-day intervals (in captivity), size 55·2–57·2 mm × 37·8–38·9 mm (oxyptera, in wild) (11), 59·9 mm × 38·3 mm (oxyptera, in captivity) or 52·1 mm × 36 mm (flavirostris), mass 40·9 g (oxyptera) or 36·5 g (flavirostris) (1); incubation c. 24–35 days by female alone (1); chicks have dark brown down above, yellowish below (whiter in Andean subspecies) with broad dark band on cheeks and mass of 22·1 g (flavirostris) or 24 g (oxyptera) at one day old (1); fledging 6–7 weeks, with young generally tended by both adults (1). Potential predators of ducklings in S of range include Southern Caracaras (Caracara plancus), Aplomado Falcons (Falco femoralis) and Peregrine Falcons (F. peregrinus) (7). Nest success 42·9% for nominate race, with nest desertion a common cause of failure (7, 1), but those nesting in parakeet nests are safe from periodic flooding and from numerous terrestrial predators (10). Sexual maturity achieved at one year old (1).

Not globally threatened (Least Concern). Generally common, even locally abundant, with overall population of nominate race in mainland South America estimated at > 1,000,000 birds (1), plus an additional 6000–11,000 pairs (or 18,000–33,000 birds) in Falkand Is during breeding bird survey of 1983–1993 (12), and perhaps 25,000–100,000 for oxyptera (1). Nominate subspecies widespread within its range; common resident on Falkland Is . Partial counts in Jul 1990 yielded 3019 birds in Argentina, 884 in Chile and 678 in Uruguay. In Peru, in N Central Cordillera, 1000+ recorded at Laguna de los Cóndores (13). Estimated 40–50 birds in Cumberland Bay, South Georgia, a small breeding population discovered in 1971 that probably originates from introduction by early whalers or immigration from Falklands, with a few records from offshore Bird I (14). Hunted intensely in winter quarters, but population does not seem seriously affected, and egg collecting, erosion from overgrazing and development are additional threats (1).

Distribution of the Yellow-billed Teal - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Yellow-billed Teal
The Cornell Lab logo
Data provided by eBird

Yellow-billed Teal

Anas flavirostris

Abundance

Estimates of relative abundance for every week of the year animated to show movement patterns. Relative abundance is the estimated average count of individuals detected by an eBirder during a 1 hour, 1 kilometer traveling checklist at the optimal time of day for each species.   Learn more about this data

Relative abundance
0.46
1.6
4.8
Week of the year
Yellow-billed Teal, Abundance map
The Cornell Lab logo
Data provided by eBird

Yellow-billed Teal

Anas flavirostris

Abundance

Relative abundance is depicted for each season along a color gradient from a light color indicating lower relative abundance to a dark color indicating a higher relative abundance. Relative abundance is the estimated average count of individuals detected by an eBirder during a 1 hour, 1 kilometer traveling checklist at the optimal time of day for each species.   Learn more about this data

Relative abundance
Year-round
0.17
1.6
6.4
Breeding season
Sep 6 - Apr 5
0.17
1.6
6.4
Non-breeding season
Jun 7 - Jul 19
0.17
1.6
6.4
Pre-breeding migratory season
Not shown
0.17
1.6
6.4
Post-breeding migratory season
Not shown
0.17
1.6
6.4
Note: Seasonal ranges overlap and are stacked in the order above; view full range in season maps.
Seasons timeline
Learn more about seasons

Recommended Citation

Carboneras, C. and G. M. Kirwan (2020). Yellow-billed Teal (Anas flavirostris), version 1.0. In Birds of the World (J. del Hoyo, A. Elliott, J. Sargatal, D. A. Christie, and E. de Juana, Editors). Cornell Lab of Ornithology, Ithaca, NY, USA. https://doi.org/10.2173/bow.yebtea1.01
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