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Fasciated Tiger-Heron Tigrisoma fasciatum Scientific name definitions

Albert Martínez-Vilalta, Anna Motis, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated February 19, 2016

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Introduction

Although widespread, Fasciated Tiger-Heron is uncommon and local throughout its range. They occur along rocky streams and rivers in subtropical forest. Frequently seen standing motionlessly on boulders or gravel in the stream’s center, they hunt primarily for fish. Although Rufescent Tiger-Heron (Tigrisoma lineatum) is somewhat similar in appearance, they prefer stagnant water and occur at lower elevations than Fasciated. The adults of these two species are distinctive, with Fasciateds appearing dark overall with narrow pale stripes throughout. The juveniles, however, are both light brown patterned with dark, and are virtually indistinguishable in the field.

Field Identification

61–71 cm; 850 g (1). Identified by being marginally smaller than T. lineatum, with shorter tarsi, shorter, more robust, slightly downcurved and generally dark bill  (maxilla black with horn-coloured tip and mandible has yellow-green base, otherwise dark), barred (not chestnut) head  and neck, uniform grey (not banded) flanks and tawny (not grey and ochre) abdomen, while the present species also has a penchant for more highland localities (although they are locally sympatric, e.g. in the foothills of the Sierra Nevada de Santa Marta, N Colombia) (2). From T. mexicanum, separated by smaller size, white-feathered throat and dark flanks and underparts. Underwing slate indistinctly barred whitish. Colour of facial skin  variable, with lores yellow to black, perhaps changing seasonally; eyes yellow; legs and feet brown. Juvenile generally duller, more prominently banded blackish and pale buff; whiter below, very closely recalling juvenile T. lineatum, but bill shorter and stouter, appearing more curved (but note very young lineatum could be identical in this respect), has more barring on flanks (but latter feature very difficult to see in the field) and three (as opposed to four) narrow white bands on tail (1). Full-adult plumage only achieved after c. 4 years, with barring slowly becoming narrower and less distinct with age. Races separated on measurements, coloration and feathering on mandible: pallescens large, is paler especially on rear underparts; has strip of feathering over base of lower mandible (like nominate fasciatum); salmoni smaller, lacks mandibular feathering.

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.

Form fasciatum formerly treated as a race of T. lineatum. Three subspecies recognized.

Subspecies

Scattered records as far as the Guianas and Amapá (NC Brazil) suggest range may be more extensive (3).


SUBSPECIES

Tigrisoma fasciatum salmoni Scientific name definitions

Distribution

Costa Rica and Panama E to NE Venezuela, and S through Andes to NW Argentina (Jujuy).

SUBSPECIES

Tigrisoma fasciatum fasciatum Scientific name definitions

Distribution

WC and SE Brazil (Mato Grosso; Rio de Janeiro to Rio Grande do Sul) and NE Argentina (Misiones).

SUBSPECIES

Tigrisoma fasciatum pallescens Scientific name definitions

Distribution

NW Argentina (Salta, Tucumán).

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

Occurs in wet premontane forest; generally found along clear-water creeks , streams and fast-flowing rivers with sand or gravel banks and forested margins. Generally recorded above 300 m (e.g. in Venezuela and Peru), generally reaching 2200 m in Colombia, c. 2150 m in E Peru (4, 5) (though see Movements) and 1200 m in Venezuela (6), but below 750 m in Central America (7).

Movement

Sedentary. In Andes, regular dispersal, mostly of juveniles, to temperate zone; in Peru, occurs up to 3300 m in semi-arid valleys of Cuzco, and possibly also in Ayacucho and Apurímac.

Diet and Foraging

Very little known. Stomach contents included armoured catfish (Loricariidae) and Odonata (8), and recently observed stalking frogs and small fish, and to take an 8–10 cm-long brown slug (5). Normally feeds alone (by Standing and Walking Slowly) (7), although individuals may be stationed at just a few hundred metres distance along suitable rivers (1) (sometimes as close as 50 m) (9), and is presumably partially nocturnal, but it also regularly feeds by day (5). Frequently observed in the open, but its generally dark coloration provides reasonable camouflage.

Sounds and Vocal Behavior

Until recently was considered to be unknown (7), but since then a loud series of “kwok” notes has been described (10) and recorded  . Furthermore, territorial song is now known to be similar to that of T. lineatum, with the first notes ascending and ending in a mooing, but the first notes in the present species are given in pairs, with the accent on the second note of each pair, whereas T. lineatum utters single, constantly ascending notes (11).

Breeding

A nest in Mato Grosso do Sul, Brazil, had a chick  in Nov; nest in tree, made of sticks (12). Nest is a platform constructed of sticks and lianas, 50–60 cm in diameter; single egg, while the chick is fed by both adults, and fledges at c. 35 days (12).

Not globally threatened (Least Concern). Previously considered Near Threatened; included in original Red Data Book (1978/79), where placed in category Indeterminate, due to scarcity of observations. No robust information available on overall status or population size; said to be local and uncommon, and generally found at low densities (7); presence in some parts of supposed range remains unconfirmed. Legally protected in Brazil, where the species is considered threatened at national level (due to forest clearance along rivers, effects of tourism and, especially, construction of hydroelectric schemes) (12), and is known from several protected areas including Amapá National Forest (3), Chapada dos Veadeiros and Iguaçu National Parks (13). Rare and patchy in Colombia, but reportedly expanding its range in highlands of Costa Rica due to increase in artificial fishponds, where recently also reported on country’s Pacific slope (7), and has been discovered in SE Honduras (at several localities within the Río Plátano Biosphere Reserve) (14) and in SE Nicaragua (Reserva Biológica Indio Maíz) (15). Furthermore, range only recently extended to encompass C Surinam (where nominally protected within Central Surinam Nature Reserve) (16), French Guiana (where recorded on three different rivers) (17) and the state of Amapá, in northernmost Brazil (3), while W of Andes, the species has recently been discovered at several sites in NW Peru (including Laquipampa Wildlife Refuge) (18). Nominate fasciatum very rare or perhaps even extinct in many parts of its range in SE Brazil, due to forest destruction, with very few known localities (some of them purely historical), in following states from N to S (Rio Grande do Sul, Santa Catarina, Paraná (8, 13), São Paulo (9), Mato Grosso do Sul (19, 20), Mato Grosso, Rio de Janeiro and Goiás) (21, 22, 23); evidence suggests may never have been numerous, but the species was recently rediscovered after almost two centuries without records in state of Rio de Janeiro  . Race salmoni considered uncommon and local in N Venezuela, where regularly found at just a couple of localities, with one sight-only record from far S of country (Amazonas) at frontier with Brazil (1). Race pallescens of Salta and Tucumán Provinces, Argentina, even less known; may also be at risk if proposed hydroelectric schemes are constructed (24).

Distribution of the Fasciated Tiger-Heron - Range Map
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Distribution of the Fasciated Tiger-Heron

Recommended Citation

Martínez-Vilalta, A., A. Motis, and G. M. Kirwan (2020). Fasciated Tiger-Heron (Tigrisoma fasciatum), 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.father1.01
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