Ciênciometria/Divulgação Científica
Traditional knowledge and perception of birds in the Parnaíba Delta environmental protection area, Northeast Brazil
Traditional knowledge and perception of birds in the Parnaíba Delta environmental protection area, Northeast Brazil
Acta Scientiarum. Biological Sciences, vol. 42, pp. 1-12, 2020
Universidade Estadual de Maringá

Recepción: 30 Abril 2019
Aprobación: 22 Noviembre 2019
Abstract: Local inhabitants retain a vast knowledge about the bird richness surrounding them, as well as many of their ethological and ecological aspects, and can identify the importance of those birds to the maintenance of ecosystem integrity. The present study sought to document the traditional knowledge retained by members of the Labino community concerning the avifauna of the Delta do Rio Parnaíba Environmental Protection Area (APA), Piauí State, Brazil. We interviewed 76 male (51% of the sample) and 74 female (49%) residents. The interviewees indicated the occurrence of 97 bird species belonging to 21 orders and 40 families. Men could identify more bird species than women. Older individuals recognize more bird species than younger members of the community. Individuals with less schooling demonstrated greater knowledge of species richness than those with more formal educations. A very significant percentage (45%, n = 68) of the interviewees reported consuming native birds, principally Aramides cajaneus, Columbina squammata, and Zenaida auriculata. A total of 48 species were perceived as having their populations reduced in recent years, principally Mimus gilvus, Icterus jamacaii, Aramides cajaneus, Turdus rufiventris, and Cacicus cela. The residents of the Labino community were therefore found to have a detailed knowledge of the local avifauna and perceived impacts caused mainly by hunting in the Parnaiba River Delta region.
Keywords: Avifauna, Hunting, Conservation, Labino community.
Introduction
Traditional knowledge is defined as that collection of knowledge and know-how concerned with natural and supernatural realms that is orally transmitted from generation to generation in traditional societies (Diegues, 2000). The preservation, recovery, and recognition of the importance of traditional knowledge can reinforce positive relationships between the inhabitants of an area and their environment, and can form the basis for fomenting activities directed towards its conservation and conscientious use, including ecotourism and bird watching (Chiwanga & Mkiramweni, 2019).
Humans have developed an incredibly diverse repertoire of interactions with birds dating back to remote times (Duncan, Blackburn, & Worthy, 2002), and birds can likewise be encountered cohabiting with human societies throughout the world (Sodhi, Şekercioğlu, Barlow, & Robinson, 2011). In that light, it is not surprising that local inhabitants detain a vast knowledge of the birds that surround them, including species richness and many other ethological and ecological aspects, and understand the enormous importance of those animals to the equilibrium and integrity of the environment they share (Alves, Leite, Souto, Bezerra, & Loures-Ribeiro, 2013).
An approximation with local inhabitants based on those aspects could aid in efficiently passing concepts linked to ecological conservation and realigning some of their cultural and daily practices, with the least interference possible, and help coordinate practical actions. Those subtle course alterations could presumably be attempted while simultaneously evaluating populations of the local fauna and observing the effects of human pressure on them (including subsistence hunting or the protection of cultivated areas), while simultaneously stimulating community participation in species conservation activities (Santos, 2019).
As such, our efforts to examine traditional knowledge combined cognitive and linguistic anthropological factors through a scientific approach that sought to interpret folk knowledge concerning the use of the regional avifauna (Tidemann & Gosler, 2011). Variations of that folk knowledge must also be considered, as traditional knowledge may vary, even within the same community, according to the age or income of individuals and/or the frequencies and manners in which they utilize or come into contact with those animals (Gichuki & Terer, 2001; Nobrega, Barbosa, & Alves, 2011). Wild birds represent one of the principal hunting/food resources in northeastern Brazil, principally due to their great diversity and the absence of large mammals (Alves, Gonçalves, & Vieira, 2012).
The present study sought to document the traditional knowledge retained by members of the Labino community concerning the avifauna of the Delta do Rio Parnaíba Environmental Protection Area (APA), Piauí State, Brazil, and test the research hypothesis that folk knowledge of the local avifauna is influenced by socio-economic factors such as gender, age, schooling, and time of residence.
Material and methods
Study area
The Labino community is located in the municipality of Ilha Grande in Piauí State (PI), and is separated from the municipality of Parnaíba (2°51'02" S and 41°46'26" W) by the PI-116 state highway. The municipality of Ilha Grande had a population (in 2015) of approximately 9211 (Institudo Brasileiro de Geografia Estatística [IBGE], 2015), and the local Residents Association indicated that the Labino community is composed of 200 families and approximately 400 residents. The community is located within the Parnaiba Delta Environmental Protection Area (APA) – created by Federal Decree no. 99.274 on August 28, 1996; the APA comprises the entire coastline of Piauí State, as well as parts of the states of Maranhão and Ceara (Figure 1). The Parnaíba Delta APA was created to protect the mouths of the Ubatuba, Timonha, and Parnaíba rivers, improve the quality of life of resident populations by orienting and disciplining local economic activities, foment ecological tourism and environmental education, and preserve local cultures and traditions (Vieira & Loiola, 2014). The regional climate is type Aw by the Koppen classification system, with a rainy season from January to June and a dry season from July through December (Bastos, Andrade Junior, & Rodrigues, 2011). The vegetation is typical regional "restinga", composed of a mosaic of three basic vegetation formations: open field (campestre), shrub, and arboreal (Santos-Filho, Almeida Jr, Soares, & Zickel, 2010).

Data collection and analysis
Data were collected during the period between November/2015 and January/2016. Similar to other ethnozoological studies (Alves et al., 2013; Alves & Souto, 2015; Van Den Bergh, Kusters, & Dietz, 2013), the investigations were undertaken using semi-structured questionnaires that included questions concerning: the socio-economic lives of the interviewees; their perceptions of the importance of the local avifauna, and the identification of local species.
One hundred and fifty local residents were interviewed, representing 37.5% of the focal population; the selection criteria was individuals older than 18. The sampling error was calculated to be 5%, with a 95% confidence interval (Bernard, 1988). To avoid biasing the information solicited (Albuquerque, Cunha, Lucena, & Alves, 2014), all of the interviews were held individually. Before each interview, the interviewees were asked to sign a Consent Form (TCLE) indicating their understanding of the project and free choice in participating. The present study was approved by the Research with Humans Ethics Committee of the Universidade Federal do Piauí – Campus Parnaíba (registry number 1.323.297).
Species identifications
The birds mentioned by the interviewees were identified to the species level using a field guide (Ridgely & Tudor, 1994; Sigrist, 2009). The taxonomic names are according to the determinations of the Brazilian Committee of Ornithological Registration for Birds (CBRO) (Piacentini et al., 2015); vernacular names follow, as provided by members of the community investigated.
The data were organized into digital archives (MS EXCEL© 2016) and the graphs were prepared at high resolution (300 dpi) with the aid of the DANIEL’s XL TOOLBOX, version 6.60 add-on open source tool (Kraus, 2014). The data were analyzed using univariate statistics to verify the existence of influences by socioeconomic factors on local ethno-ornithological knowledge. Statistical analyses were performed using SPSS© version 23 software (IBM© Corp., 2014), consistently using a significance level of 5% (p < 0.05).
Results and discussion
Socioeconomic aspects
The sample population was composed of 150 interviewees (51% men [n = 76] and 49% women [n = 74]); their ages varied from 18 to 87. In general, participant schooling levels were quite low, with 11.33% (n = 17) being illiterate while 40.67% did not complete grammar school. Family incomes in the Labino community varied between 1 and 4 minimum wages (the Brazilian minimum wage in May 2016 was ~ USD $248), but most of the informants (n=92; 61%) earned approximately 1 to 2 minimum wages. The municipality of Ilha Grande had a mean human development index (MHDI) of 0.563 in 2010. The gap between the MHDI of the municipality and the maximum value of that index (1.0) was reduced by 73.45% between 2000 and 2010 (Brasil, 2013). The socioeconomic data of the interviewees are summarized in Table 1.
Traditionally, wildlife is valued beyond its economic and simple utilitarian importance when cultural factors associated with their use are considered. On the other hand, there are aspects more directly anthropocentric and utilitarian when birds are recognized as resources to be used for an individual’s own benefit (Costa-Neto, Santos Fita, & Clavijo, 2007). In that sense, social, economic, and cultural factors play an important role in how individuals and communities use those natural resources, leading to a very widely discussed conflict: development versus species preservation (Nobrega et al., 2011).
Local knowledge of the avifauna and social aspects
The Parnaíba Delta has a rich and diversified avifauna, as 97 bird species were cited by the interviewees (individual mean of 8.8 ± 4.87 s.e. [standard error]) from the Labino community in the municipality of Ilha Grande/PI. The birds recognized by the interviewees belonged to 85 genera, 40 families, and 21 orders (Table 2). Although traditional knowledge can often be informative in terms of new species (Cozzuol et al., 2013), all of the species mentioned in the ethno-ornithological survey had been previously recorded in earlier scientific surveys (Guzzi et al., 2015); it is impressive, however, that approximately 60% of the birds recorded in scientific surveys (of a total of 161 species) are recognized on a day-to-day basis by members of the Labino community.
| Profile | n | % |
| Gender | ||
| Female | 74 | 49% |
| Male | 76 | 51% |
| Age | ||
| Less than 30 years old | 45 | 30% |
| 30 - 39 | 28 | 19% |
| 40 - 49 | 28 | 19% |
| 50 - 59 | 23 | 15% |
| 60 or older | 19 | 13% |
| Not mentioned | 7 | 5% |
| Residence time in the community | ||
| < 5 years | 9 | 6% |
| 5 - 10 years | 19 | 13% |
| 11 - 15 years | 12 | 8% |
| 16 - 20 years | 24 | 16% |
| 21 - 25 years | 13 | 9% |
| 26 - 30 years | 18 | 12% |
| 60 or older | 42 | 28% |
| Not mentioned | 13 | 9% |
| Schooling | ||
| Illiterate | 17 | 11% |
| Elementary school incomplete | 48 | 32% |
| Elementary school complete | 13 | 9% |
| Middle school incomplete | 17 | 11% |
| Middle school complete | 46 | 31% |
| High school incomplete | 2 | 1% |
| High school complete | 7 | 5% |
| Taxa | Piacentini et al. (2015) | (Informants) | n | % |
| Tinamidae Gray, 1840 | ||||
| Crypturellus undulatus (Temminck, 1815) | Undulated Tinamou | Jaó | 10 | 7% |
| Crypturellus parvirostris (Wagler, 1827) | Small-billed Tinamou | Nambúd | 7 | 5% |
| Anatidae Leach, 1820 | ||||
| Dendrocygna viduata (Linnaeus, 1766) | White-faced Whistling-Duck | Paturia d | 12 | 8% |
| Anasba hamensis Linnaeus, 1758 | White-cheeked Pintail | Marrecaa d | 35 | 23% |
| Cracidae Rafinesque, 1815 | ||||
| Penelope superciliaris Temminck, 1815 | Rusty-margined Guan | Jacupemba | 4 | 3% |
| Ortalis superciliaris (Gray, 1867) | Buff-browed Chachalaca | Aracuã | 1 | 1% |
| Podicipedidae Bonaparte, 1831 | ||||
| Tachybaptus dominicus (Linnaeus, 1766) | Least Grebe | Mergulhão-pequeno | 6 | 4% |
| Podilymbus podiceps (Linnaeus, 1758) | Pied-billed Grebe | Pecaparad | 3 | 2% |
| Phalacrocoracidae Reichenbach, 1849 | ||||
| Nannopterum brasilianus (Gmelin, 1789) | Neotropic Cormorant | Biguá | 1 | 1% |
| Ardeidae Leach, 1820 | ||||
| Tigrisoma lineatum (Boddaert, 1783) | Rufescent Tiger-Heron | Socóa d | 1 | 1% |
| Nyctanassa violacea (Linnaeus, 1758) | Yellow-crowned Night-Heron | Tamatiãoa d | 21 | 14% |
| Butorides striata (Linnaeus, 1758) | Striated Heron | Socozinho | 25 | 17% |
| Bubulcus ibis (Linnaeus, 1758) | Cattle Egret | Garça-pequenaa d | 55 | 37% |
| Ardea alba Linnaeus, 1758 | Cattle Egret | Garça-grandea d | 5 | 3% |
| Egretta caerulea (Linnaeus, 1758) | Little Blue Heron | Garça-parda | 3 | 2% |
| Threskiornithidae Poche, 1904 | ||||
| Eudocimus ruber (Linnaeus, 1758) | Scarlet Ibis | Guará | 9 | 6% |
| Theristicus caudatus (Boddaert, 1783) | Buff-necked Ibis | Curicaca | 4 | 3% |
| Cathartidae Lafresnaye, 1839 | ||||
| Cathartes aura (Linnaeus, 1758) | Turkey Vulture | Urubu-de-cabeça-vermelha | 3 | 2% |
| Cathartes burrovianus Cassin, 1845 | Lesser Yellow-headed Vulture | Urubu-de-cabeça-amarela | 2 | 1% |
| Coragyps atratus (Bechstein, 1793) | Black Vulture | Urubu-de-cabeça-preta d | 55 | 37% |
| Accipitridae Vigors, 1824 | ||||
| Rostrhamus sociabilis (Vieillot, 1817) | Snai lKite | Gavião-caramujeiro | 22 | 15% |
| Urubitinga urubitinga (Gmelin, 1788) | Great Black Hawk | Gavião-preto d | 1 | 1% |
| Rupornis magnirostris (Gmelin, 1788) | Roadside Hawk | Gavião-carijód | 1 | 1% |
| Falconidae Leach, 1820 | ||||
| Caracara plancus (Miller, 1777) | Southern Caracara | Carcará | 15 | 10% |
| Herpetotheres cachinnans (Linnaeus, 1758) | Laughing Falcon | Acauã | 2 | 1% |
| Aramidae Bonaparte, 1852 | ||||
| Aramus guarauna (Linnaeus, 1766) | Limpkin | Carãoa d | 28 | 19% |
| Rallidae Rafinesque, 1815 | ||||
| Aramides cajaneus (Statius Muller, 1776) | Gray-necked Wood-Rail | Siricoraa d | 30 | 20% |
| Gallinula galeata (Lichtenstein,1818) | Common Gallinule | Frango-d'águaa d | 23 | 15% |
| Porphyriops melanops (Vieillot, 1819) | Spot-flanked Gallinule | Capote-d'água | 11 | 7% |
| Porphyrio martinicus (Linnaeus, 1766) | Purple Gallinule | Frango-d'água | 6 | 4% |
| Charadriidae Leach, 1820 | ||||
| Vanellus chilensis (Molina, 1782) | Southern Lapwing | Tetéud | 22 | 15% |
| Scolopacidae Rafinesque, 1815 | ||||
| Numeniu sphaeopus (Linnaeus, 1758) | Eurasian Whimbrel | Pirão-gordo d | 4 | 3% |
| Tringa melanoleuca (Gmelin, 1789) | Greater Yellowlegs | Maçarico-grande | 2 | 1% |
| Calidris alba (Pallas, 1764) | Sanderling | Maçarico-branco | 21 | 14% |
| Calidris minutilla (Vieillot, 1819) | Least Sandpiper | Maçarico-pequeno | 4 | 3% |
| Jacanidae Chenu & Des Murs, 1854 | ||||
| Jacana jacana (Linnaeus, 1766) | Wattled Jacana | Jaçanãa | 9 | 6% |
| Laridae Rafinesque, 181 | ||||
| Chroicocephalus cirrocephalus (Vieillot, 1818) | Gray-hooded Gull | Gaivotad | 11 | 7% |
| Phaetusa simplex (Gmelin, 1789) | Large-billed Tern | Trinta-réis-grande | 2 | 1% |
| Columbidae Leach, 1820 | ||||
| Columbina talpacoti (Temminck, 1811) | Ruddy Ground-Dove | Rolinha-sangue-de-boi a d | 24 | 16% |
| Columbina squammata (Lesson, 1831) | Scaled Dove | Fogo-apagou a d | 1 | 1% |
| Columbina picui (Temminck, 1813) | Picui Ground-Dove | Rolinha-branca a d | 109 | 73% |
| Columbina passerina (Linnaeus, 1758) | Common Ground-Dove | Rolinha-cinza d | 20 | 13% |
| Columba livia Gmelin, 1789 | Rock Pigeon | Pombo | 3 | 2% |
| Patagioenas picazuro (Temminck, 1813) | Picazuro Pigeon | Asa-brancaa | 2 | 1% |
| Leptotila verreauxi Bonaparte, 1855 | White-tipped Dove | Juriti | 3 | 2% |
| Zenaida auriculata (Des Murs, 1847) | Eared Dove | Avoantea d | 17 | 11% |
| Psittacidae Rafinesque, 1815 | ||||
| Eupsittula cactorum (Kuhl, 1820) | Cactus Parakeet | Periquito-da-caatinga d | 6 | 4% |
| Forpus xanthopterygius (Spix, 1824) | Blue-winged Parrotlet | Tuimd | 6 | 4% |
| Thectocercus acuticaudatus (Vieillot, 1818) | Blue-crowned Parakeet | Periquito-de-testa-azul d | 6 | 4% |
| Amazona aestiva (Linnaeus, 1758) | Turquoise-fronted Parrot | Papagaiod | 8 | 5% |
| Cuculidae Leach, 1820 | ||||
| Piaya cayana (Linnaeus, 1766) | Squirrel Cuckoo | alma-de-gato | 4 | 3% |
| Coccyzus euleri Cabanis, 1873 | Pearly-breasted Cuckoo | Papa-lagarta a d | 2 | 1% |
| Crotophaga major Gmelin, 1788 | Greater Ani | Gorgoróa d | 17 | 11% |
| Crotophaga ani Linnaeus, 1758 | Smooth-billed Ani | Anud | 47 | 31% |
| Guira guira (Gmelin, 1788) | Guira Cuckoo | Piririguá d | 21 | 14% |
| Tytonidae Mathews, 1912 | ||||
| Tyto furcata (Temminck, 1811) | American Barn Owl | Corujaa | 10 | 7% |
| Strigidae Leach, 1820 | ||||
| Glaucidium brasilianum (Gmelin, 1788) | Ferruginous Pygmy-Owl | Caburé | 11 | 7% |
| Nyctibiidae Chenu& Des Murs, 1851 | ||||
| Nyctibius griseus (Gmelin, 1789) | Common Potoo | Mãe-da-lua d | 1 | 1% |
| Caprimulgidae Vigors, 1825 | ||||
| Nyctidromus albicollis (Gmelin, 1789) | Common Pauraque | Bacurau | 1 | 1% |
| Podager nacunda (Vieillot, 1817) | Nacunda Nighthawk | Corucão | 1 | 1% |
| Trochilidae Vigors, 1825 | ||||
| Amazilia leucogaster (Gmelin, 1788) | Plain-bellied Emerald | Beija-flor-de-barriga-brancad | 21 | 14% |
| Alcedinidae Rafinesque, 1815 | ||||
| Megaceryle torquata (Linnaeus, 1766) | Ringed Kingfisher | Martim-pescador-grande | 2 | 1% |
| Chloroceryle amazona (Latham, 1790) | Amazon Kingfisher | Martim-pescador-verde | 8 | 5% |
| Bucconidae Horsfield, 1821 | ||||
| Nystalus maculatus (Gmelin, 1788) | Spot-backed Puffbird | Bico-de-latão | 2 | 1% |
| Picidae Leach, 1820 | ||||
| Melanerpes candidus (Otto, 1796) | White Woodpecker | Pica-pau-branco d | 1 | 1% |
| Veniliorni spasserinus (Linnaeus, 1766) | Little Woodpecker | Pica-pau-anão | 16 | 11% |
| Colaptes melanochloros (Gmelin, 1788) | Green-barred Woodpecker | Pica-pau-verde | 2 | 1% |
| Celeus flavescens (Gmelin, 1788) | Blond-crested Woodpecker | Pica-pau-amarelo d | 2 | 1% |
| Campephilus melanoleucos (Gmelin, 1788) | Crimson-crested Woodpecker | Pica-pau-vermelho d | 3 | 2% |
| Thamnophilidae Swainson, 1824 | ||||
| Taraba major (Vieillot, 1816) | Great Antshrike | Choró-boi d | 2 | 1% |
| Furnariidae Gray, 184 | ||||
| Furnarius rufus (Gmelin, 1788) | Rufous Hornero | João-de-barro | 1 | 1% |
| Tyrannidae Vigors, 1825 | ||||
| Pitangus sulphuratus (Linnaeus, 1766) | Great Kiskadee | Bem-te-via d | 97 | 65% |
| Tyrannus melancholicus Vieillot, 1819 | Tropical Kingbird | Severinaa | 11 | 7% |
| Fluvicola nengeta (Linnaeus, 1766) | Masked Water-Tyrant | Lavadeira-mascarada | 7 | 5% |
| Corvidae Leach, 1820 | ||||
| Cyanocorax cyanopogon (Wied, 1821) | White-naped Jay | Cancão d | 5 | 3% |
| Troglodytidae Swainson, 1831 | ||||
| Troglodytes musculus Naumann, 1823 | Southern House Wren | Rouxinol | 2 | 1% |
| Turdidae Rafinesque, 1815 | ||||
| Turdus rufiventris Vieillot, 1818 | Rufous-bellied Thrush | Sabiá-verdadeiraa d | 71 | 47% |
| Mimidae Bonaparte, 1853 | ||||
| Mimus saturninus (Lichtenstein, 1823) | Chalk-browed Mockingbird | Sabiá-da-mata d | 13 | 9% |
| Mimus gilvus (Vieillot, 1807) | Tropical Mockingbird | Sábia-da-praia d | 5 | 3% |
| Thraupidae Cabanis, 1847 | ||||
| Coryphospingus pileatus (Wied, 1821) | Pileated Finch | Tico-tico | 5 | 3% |
| Tangara sayaca (Linnaeus, 1766) | Sayaca Tanager | Sanhaçúd | 2 | 1% |
| Paroaria dominicana (Linnaeus, 1758) | Red-cowled Cardinal | Galo-de-campina d | 18 | 12% |
| Sicali flaveola (Linnaeus, 1766) | Saffron Finch | Canário-da-terra | 1 | 1% |
| Volatinia jacarina (Linnaeus, 1766) | Blue-black Grassquit | Tiziu | 1 | 1% |
| Sporophila lineola (Linnaeus, 1758) | Lined Seedeater | Bigode | 12 | 8% |
| Sporophila bouvreuil (Statius Muller, 1776) | Copper Seedeater | Caboclinho | 1 | 1% |
| Coereba flaveola (Linnaeus, 1758) | Bananaquit | Sibiti | 2 | 1% |
| Cardinalidae Ridgway, 1901 | ||||
| Cyanoloxia brissonii (Lichtenstein, 1823) | Ultramarine Grosbeak | Azulão | 1 | 1% |
| Parulidae Wetmore, Friedmann, Lincoln, Miller, Peters, van Rossem, Van Tyne & Zimmer 1947 | ||||
| Basileuterus culicivorus (Deppe, 1830) | Golden-crowned Warbler | Pula-pula | 3 | 2% |
| Icteridae Vigors, 1825 | ||||
| Procacicus solitarius (Vieillot, 1816) | Solitary Black Cacique | Iraúna | 1 | 1% |
| Cacicus cela (Linnaeus, 1758) | Yellow-rumped Cacique | Xexéud | 29 | 19% |
| Icterus pyrrhopterus (Vieillot, 1819) | Variable Oriole | Primaverad | 7 | 5% |
| Icterus jamacaii (Gmelin, 1788) | Campo Troupial | Corrupião d | 71 | 47% |
| Gnorimopsar chopi (Vieillot, 1819) | Chopi Blackbird | Chico-preto/graúna d | 26 | 17% |
| Sturnella superciliaris (Bonaparte, 1850) | White-browed Meadowlark | Papa-arroz | 2 | 1% |
| Fringillidae Leach, 1820 | ||||
| Euphonia chlorotica (Linnaeus, 1766) | Purple-throated Euphonia | Vim-vim | 4 | 3% |
| Passeridae Rafinesque, 1815 | ||||
| Passer domesticus (Linnaeus, 1758) | House Sparrow | Pardald | 54 | 36% |
| Total = 97 Species |
Passeriformes were the best represented among the species reported by the interviewees, comprising 29% (n = 28 species) of the total number of species cited, followed by the orders Pelecaniformes, Charadriiformes, and Columbiformes (8%; n = 8 species each); Gruiformes, Cuculiformes, and Piciformes (5%; n = 5 species each). This expressive total of Passeriformes may reflect a preference of the interviewees for singing birds, principally the families Icteridae and Turdidae (species kept as pets), and the Tyrannidae, as well as the abundance of species within that family.
The order Passeriformes consistently shows the greatest species richness in ethno-ornithological studies of the uses and commercialization of birds (Barbosa, Silva, Medeiros, & Chaves, 2014; Galvagne-Loss, Costa-Neto, & Flores, 2014). This order includes birds that are appreciated for their singing and plumage in practically all areas of the tropics, and it is also the most representative order among neotropical birds, with 5,739 known species (Silvius, Bodmer, & Fragoso, 2004) – which helps explain their frequent citations by the interviewees from the Labino community. Columbiformes represent important food resources throughout South America, and species of this order are generally well-known by local human inhabitants (Souza & Alves, 2014). The Columbiformes are important targets for local hunters in northeastern Brazil, and all of its species are killed, captured, and illegally sold for their bush meat. Species of the orders Pelecaniformes and Gruiformes include large birds and those with significant diurnal activities in aquatic environments, which facilitates their observation and recognition by humans (Alves et al., 2012; Souza & Alves, 2014).
The most representative families were Columbidae and Traupidae (8 species each); followed by Ardeidae and Icteridae (6 species); Cuculidade and Picidae (5 species); Rallidae, Scolopacidae, and Psittacidae (4 species). The species with the largest numbers of citations were Columbina picui (n = 109; 73%), Pitangus sulphuratus (n = 97; 65%), Turdus rufiventris, Icterus jamacaii (ambas, n = 71; 47%), Bubulcus ibis and Coragyps atratus (n = 55; 37% each), and Passer domesticus (n = 54; 36%).
Some of the families mentioned as having high species richness in the present study were likewise well-represented in other ornithological surveys in the Parnaíba Delta region (Guzzi et al., 2012, 2015), principally the families Scolopacidae, Ardeidae, and Icteridae in terms of species richness.
Although the richness curve of known species (S(est)) is asymptotic, it is only slightly inclined, and shows a tendency towards stabilization (Figure 2). We were apparently able to record essentially the entire inventory of birds known to the local residents, as Chao2 estimated a richness of approximately 104 species (s.e.= ±5.36 spp.) and second-order Jackknife (Jack2) estimated approximately 114 species (s.e. = 0). The curves of both estimators achieved asymptote with 86 interviewees (Jack2) and 104 interviewees (Chao2) (Figure 2). Consequently, the species inventory demonstrated a sampling effort of 92.3% (comparing S(est) with Chao2) or 84.21% (comparing S(est) with Jack2).

Men recognize more local bird species than women (mean per man = 9.76 ± 5.11; mean per woman = 7.57 ± 4.37; median per man = 9, median per woman = 6). These differences were significant (Mann-Whitney U = 3,613.5; d.f. = 1; p = 0.002; mean ranking (men = 86.05; women = 64.67) (Figure 3A).
The fact that men recognized more bird species than women was not surprising, as hunting activities that involve birds are more frequently or exclusively undertaken by men throughout the tropics, increasing the chances of males utilizing or being aware of more kinetic resources and the ethnoecological aspects of bird species (Alves et al., 2012; Van Vliet et al., 2014). A study undertaken in Pernambuco State (NE Brazil) demonstrated that men retain greater local knowledge about shorebirds and migratory birds than women, which may be related to greater male participation in fishing activities undertaken near avifauna feeding and resting areas (Andrade, Silva-Andrade, Lyra-Neves, Albuquerque, & Telino-Júnior, 2016).
Transgenerational diffusion of ethnozoological knowledge has been cited by a number of authors (Alves & Souto, 2015; Fita, Neto, & Schiavetti, 2010; Souto, Barboza, Rocha, Alves, & Mourão, 2012). We indirectly identified this phenomenon in relation to local ethno-ornithological knowledge, as older individuals generally recognized more bird species than younger members of the community, although this correlation was quite weak (Pearson correlation = 0.164; p = 0.05) (Figure 3B).
The greater levels of knowledge of older individuals corroborated earlier studies focusing on the capture and commercial uses of the tropical fauna (Lindsey et al., 2013; Pangau-Adam, Noske, & Muehlenberg, 2012; Souza & Alves, 2014), suggesting that local knowledge concerning the native fauna is directly influenced by a synergy of factors, including, principally, knowledge transmitted from older individuals to younger relatives, as well as the involvement of a given person in activities that favor frequent contacts with the regional fauna (as, for example, agriculture, land clearing, hunting, and the commercialization of animal products).

Educational levels likewise influences local knowledge about birds (Kruskal-Wallis H = 14.21; d.f. = 2; p < 0.001) (Figure 3C). This difference was observed between individuals with low levels of schooling (illiterate individuals or those that did not finish grammar school) and community members with more education (middle schooling completed or higher) (Dunn post-hoc test, p < 0.05) – with individuals with less schooling demonstrating greater knowledge of species richness than those with more formal educations (Mean ranking low schooling = 88.32, and median = 10; Mean ranking higher education = 58.5, and median = 6). These results demonstrate that a low level of formal schooling do not necessarily imply a poor knowledge of species of the local fauna; these results were similar to those found while studying reproductive aspects of the Psittacidae (Saiki, Guido, & Cunha, 2009) and the ecology of the mangrove crab Ucides cordatus (Cortês, Zappes, & Di Beneditto, 2014) – and may reflect teaching/learning processes – as most school books stress exotic faunas, and more applied students may have less contact with the local avifauna. Time of residence in the community was not found to influence knowledge concerning bird species richness (Kruskal-Wallis H = 7.22; d.f. = 3; p = 0.065) (Figure 3D).
Perceptions of impacts on the avifauna, and the use of birds as bush meat
Residents of the Labino community indicated hunting (68%, n=45) as the principle anthropogenic factor impacting the local avifauna. Other factors mentioned were: forest clearing (7% of the respondents), keeping birds as pets (6%), and the illegal commerce in live or dead birds (3%). The predominant perception of hunting as having the greatest impact on the local avifauna is presumably associated with the ample popularity of that activity in northern and northeastern Brazil – areas where birds are frequently converted into bush meat, medicinal products, pets, and adornments (Alves, Lopes, & Alves, 2016; Nascimento, Czaban, & Alves, 2015).
Twenty-three bird species are consumed by the residents of Labino (Table 2), with Aramides cajaneus (Siricora), belonging to the family Rallidae, being the most cited (n=21; 14% of the interviewees), followed by the columbids Columbina squammata (Rolinha-fogo-apagou) (n=19; 13 %) and Zenaida auriculata (Avoante) (n=13; 9%). Columbids, tinamids and birds associated with aquatic environments (e.g., Anseriformes, Gruiformes) were previously identified as preferential hunting targets in different parts of the tropical Americas (Bucher, 1982; Souza & Alves, 2014).
Some bird species can be harvested in large numbers during a single hunting expedition, although they do not present large volumes of meat per individual, nor are they especially appreciated in terms of their flavors, as for example most of the columbids (Bezerra, Araújo, & Alves, 2012; Von Ihering, 1935). Zenaida auriculata, Columbina spp., Anas bahamensis and Aramides cajaneus were frequently mentioned by the interviewees in that context. There was no influence of gender (Mann-Whitney U = 3.074, p > 0.05), age (Pearson correlation, p > 0.05), schooling (Kruskal-Wallis H, p > 0.05), or time of residence (Kruskal-Wallis H, p > 0.05) on the richness of bird species consumed by the interviewees.
Perception concerning avifauna population reductions
A total of 48 bird species were perceived as having their populations reduced in recent years (Table 2). The species most cited in this sense by the interviewees were: Mimus gilvus (Sabiá-da-praia) (n=15), Icterus jamacaii (Corrupião) (n=13), Aramides cajaneus (Siricora) (n=12), Turdus rufiventris (Sabiá-laranjeira) (n=9), Cacicus cela (Xexéu), Pitangus sulphuratus (Bem-te-vi) (n=8), Anas bahamensis (Marreca) (n=6), Columbina picui (Rolinha branca) (n=5), Vanellus chilensis (Quero-quero), and Tangara sayaca (Sanhaçu) (n=4). With the exception of Aramides cajaneus, the diminishing species normally show only low sensitivity to environmental alterations and considerable plasticity in terms of their tolerance of anthropogenic impacts (according to the interviewees) (Silva, Souza, Bieber, & Carlos, 2003).
The species cited as demonstrating population reductions are not considered threatened species (Instituto Chico Mendes de Conservação da Biodiversidade [ICMbio], 2018) by the International Union for the Conservation of Nature (IUCN, 2019), being classified in the “less concern” conservation category (category LC) (IUCN, 2019). The red list, however, considers species populations throughout their entire distribution range, even while some local populations could be depleted or eradicated. Ecological studies of bird populations in the Parnaiba Delta are urgently needed in light of the information provided by local residents.
The socioeconomic aspects of the residents of the Labino community, such as their gender (Mann-Whitney U, p > 0.05), age (Pearson correlation, p > 0.05), levels of schooling (Kruskal-Wallis H, p > 0.05), and time of residents in the community (Kruskal-Wallis H, p > 0.05) were not found to influence their perception of reduced species richness.
Conclusion
The information obtained in the present study demonstrated that the residents of the Labino community possess a detailed knowledge of the local avifauna and perceive impacts caused mainly by hunting – suggesting that those observers should be included when developing strategies for bird conservation through interactions with governmental institutions, and scientists. Conservation plans must seek to minimize impacts on bird species, and lists and illustrations of local bird species should be produced to complement biology studies in regional schools and include local animals – as schoolbooks generally do not contain any information about regional species and landscapes.
Acknowledgements
The authors thank the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for its financial support, and all of the participants from the Labino community in the municipality of Ilha Grande, PI, for their collaboration in this research project.
References
Albuquerque, U. P., Cunha, L. V. F. C., Lucena, R. F. P., & Alves, R. R. N. (2014). Methods and Techniques in Ethnobiology and Ethnoecology. New York, NY: Humana Press. doi: 10.1007/978-1-4614-8636-7
Alves, M. M., Lopes, S. F., & Alves, R. R. N. (2016). Wild vertebrates kept as pets in the semiarid region of Brazil. Tropical Conservation Science, 9(1), 354–368. doi. 10.1177/194008291600900119
Alves, R. R. N., & Souto, W. M. S. (2015). Ethnozoology: A Brief Introduction. Ethnobiology and Conservation, 4, 1–13. doi: 10.15451/ec2015-1-4.1-1-13
Alves, R. R. N., Gonçalves, M. B. R., & Vieira, W. L. S. (2012). Caça, uso e conservação de vertebrados no semiárido brasileiro. Tropical Conservation Science, 5(3), 394–416. doi: 10.1177/194008291200500312
Alves, R. R. N., Leite, R. C. L., Souto, W. M. S., Bezerra, D. M. M., & Loures-Ribeiro, A. (2013). Ethno-ornithology and conservation of wild birds in the semi-arid Caatinga of northeastern Brazil. Journal of Ethnobiology and Ethnomedicine, 9(14), 1–29. doi: 10.1186/1746-4269-9-14
Andrade, L. P., Silva-Andrade, H. M. L., Lyra-Neves, R. M., Albuquerque, U. P., & Telino-Júnior, W. R. (2016). Do artisanal fishers perceive declining migratory shorebird populations? Journal of Ethnobiology and Ethnomedicine, 12(16), 1–11. doi: 10.1186/s13002-016-0087-x
Barbosa, E. D. O., Silva, M. G. B., Medeiros, R. O., & Chaves, M. F. (2014). Atividades cinegéticas direcionadas à avifauna em áreas rurais do município de Jaçanã, Rio Grande do Norte, Brasil. Biotemas, 27(3), 175–190. doi: 10.5007/2175-7925.2014v27n3p175
Bastos, E. A., Andrade Junior, A. S., & Rodrigues, B. H. N. (2011). Boletim agrometeorológico de 2010 para o município de Parnaíba, Piauí. Teresina, PI: Embrapa Meio-Norte.
Bernard, H. R. (1988). Research methods in cultural anthropology. Newbury Park, CA: Sage.
Bezerra, D. M. M., Araújo, H. F. P., & Alves, R. R. N. (2012). Captura de aves silvestres no semiárido brasileiro: técnicas cinegéticas e implicações para conservação. Tropical Conservation Science, 5(1), 50–66. doi: 10.1177/194008291200500106
Brasil. (2013). Atlas do Desenvolvimento Humano no Brasil 2013, Ilha Grande – PI. Brasília, DF: PNUD. Retrieved from http://www.atlasbrasil.org.br
Bucher, E. H. (1982). Colonial breeding of the Eared Dove (Zenaida auriculata) in northeastern Brazil. Biotropica, 14(4), 255–261. doi: 10.2307/2388083
Chiwanga, F. E., & Mkiramweni, N. P. (2019). Ethno-ornithology and onomastics in the Natta community, Serengeti district, Tanzania. Heliyon, 5(10), 1–6. doi: 10.1016/j.heliyon.2019.e02525
Cortês, L. H. O., Zappes, C. A., & Di Beneditto, A. P. M. (2014). Ethnoecology, gathering techniques and traditional management of the crab Ucides cordatus Linnaeus, 1763 in a mangrove forest in south-eastern Brazil. Ocean & Coastal Management, 93, 129–138. doi: 10.1016/j.ocecoaman.2014.03.021
Costa-Neto, E. M., Santos Fita, D., & Clavijo, M. (2007). Manual de Etnozoología: una guia teórico-prática para investigar la interconexión del ser humano con los animales. Valencia, ES: Tundra.
Cozzuol, M. A., Clozato, C. L., Holanda, E. C., Rodrigues, F. H. G., Nienow, S., Thoisy, B., … Santos, F. R. (2013). A new species of tapir from the Amazon. Journal of Mammalogy, 94(6), 1331–1345. doi: 10.1644/12-MAMM-A-169.1
Decreto n° 99.274, de 6 de junho de 1990. (1996, 28 de Agosto). Dispõe sobre a criação da Área de Proteção Ambiental Delta do Parnaíba, nos Estados do Piauí, Maranhão e Ceará. Brasília, DF: Diário Oficial da República Federativa do Brasil.
Diegues, A. C. (2000). Os saberes tradicionais e a biodiversidade no Brasil. In A. C. Diegues (Org.), Biodiversidade e Comunidades Tradicionais no Brasil (pp. 30–35). São Paulo: Nupaub-USP.
Duncan, R. P., Blackburn, T. M., & Worthy, T. H. (2002). Prehistoric bird extinctions and human hunting. Proceedings of the Royal Society B - Biological Sciences, 269(1490), 517–521. doi: 10.1098/rspb.2001.1918
Fita, D. S., Neto, E. C. M., & Schiavetti, A. (2010). “Offensive” snakes: cultural beliefs and practices related to snakebites in a Brazilian rural settlement. Journal of Ethnobiology and Ethnomedicine, 6(13), 1–13. doi: 10.1186/1746-4269-6-13
Galvagne-Loss, A. T., Costa-Neto, E. M., & Flores, F. M. (2014). Aves silvestres utilizadas como recurso trófico pelos moradores do povoado de Pedra Branca, Santa Teresinha, Bahia, Brasil. Gaia Scientia, 1–14.
Gichuki, N., & Terer, T. (2001). Significance of indigenous knowledge and values of birds in promoting biodiversity conservation in Kenya. Ostrich Suplement, 15, 153–157.
Guzzi, A., Tavares, A. A., Santos, A. G. S., Cardoso, C. O., Gomes, D. N., Machado, J. L. C., … Batista, S. C. A. (2012). Diversidade de aves do Delta do Parnaíba, litoral piauiense. In A. Guzzi (Org.), Biodiversidade do Delta do Parnaíba, litoral piauiense (p. 291–327). Parnaíba, PI: Edufpi.
Guzzi, A., Tavares, A. A., Santos, A. G. S., Gomes, D. N., Ribeiro, A. S. N., Santos, F. C. V., & Vasconcelos, F. (2015). Avifauna da APA (Área de Proteção Ambiental) Delta do Parnaíba. In WMS Magalhães, M. O. M. Neto, A. Guzzi, R. A. Galeno, G. F. Gondolo, & M. A. G. P. Gondolo (Eds.), Guia da Biodiversidade do Delta do Parnaíba (p. 13–65). Teresina, PI: Edufpi.
IBM. Corp. (2014). IBM SPSS Statistics for Windows Version 23. Armonk, NY: IBM. Corp.
Instituto Brasileiro de Geografia Estatística [IBGE]. (2015). Estimativa da população 2015 de Ilha Grande – PI. Retrieved from www.cidades.ibge.gov.br/
Instituto Chico Mendes de Conservação da Biodiversidade [ICMbio]. (2018). Aves. In ICMBio (Ed.), Livro vermelho da fauna brasileira ameaçada de extinção (Vol. 3, p. 709). Brasília, DF: ICMBio. Retrieved from http://www.icmbio.gov.br/portal/biodiversidade/fauna-brasileira/lista-de-especies.html.
International Union for Conservation of Nature [IUCN]. (2019). TheIUCN Red List of Threatened Species. Version 2019-2. Retrieved from www.iucnredlist.org
Kraus, D. (2014). Consolidated data analysis and presentation using an open-source add-in for the Microsoft Excel® spreadsheet software. The European Medical Writers Association, 23(1), 25–28. doi: 10.1179/2047480613Z.000000000181
Lindsey, P. A., Balme, G., Becker, M., Begg, C., Bento, C., Bocchino, C., … Zisadza-Gandiwa, P. (2013). The bushmeat trade in African savannas: impacts, drivers, and possible solutions. Biological Conservation, 160, 80–96. doi: 10.1016/j.biocon.2012.12.020
Nascimento, C. A. R., Czaban, R. E., & Alves, R. R. N. (2015). Trends in illegal trade of wild birds in Amazonas state, Brazil. Tropical Conservation Science, 8(4), 1098–1113. doi: 10.1177/194008291500800416
Nobrega, V. A., Barbosa, J. A. A., & Alves, R. R. N. (2011). Utilização de aves silvestres por moradores do município de Fagundes , Semiárido paraibano : uma abordagem etno-ornitológica. Sitientibus Série Ciências Biológicas, 11(2), 165–175. doi: 10.13102/scb106
Pangau-Adam, M., Noske, R., & Muehlenberg, M. (2012). Wildmeat or Bushmeat? subsistence hunting and commercial harvesting in Papua (West New Guinea), Indonesia. Human Ecology, 40(4), 611–621. doi: 10.1007/s10745-012-9492-5
Piacentini, V. Q., Aleixo, A., Agne, C. E., Maurício, G. N., Pacheco, J. F., Bravo, G. A., … Cesari, E. (2015). Annotated checklist of the birds of Brazil by the Brazilian Ornithological Records Committee. Revista Brasileira de Ornitologia, 23(2), 91–298.
Ridgely, R. S., & Tudor, G. (1994). The birds of South America. Oxford, UK: University Press.
Saiki, P. T. O., Guido, L. d. F. E., & Cunha, A. M. d. O. (2009). Etnoecologia, etnotaxonomia e valoração cultural de Psittacidae em distritos rurais do Triângulo Mineiro, Brasil. Revista Brasileira de Ornitologia, 17(1), 41–52.
Santos, S. S. (2019). Conhecimento tradicional e utilização da fauna silvestre em São José da Lagoa Tapada, Paraíba, Brasil. Etnobiología, 17(1), 31–48.
Santos-Filho, F. S., Almeida Jr, E. B., Soares, C. J. R. S., & Zickel, C. S. (2010). Fisionomias das restingas do Delta do Parnaíba, Nordeste, Brasil. Revista Brasileira de Geografia Física, 3(3), 218–227. doi: 10.26848/rbgf.v3.3.p218-227
Sigrist, T. (2009). Guia de campo - Avifauna brasileira: descrição das espécies. São Paulo, SP: Avis Brasilis.
Silva, J. M. C., Souza, M. A., Bieber, A. G. D., & Carlos, C. J. (2003). Aves da Caatinga: status, uso do habitat e sensitividade. In I. R. Leal, M. Tabarelli & J. M. C. Silva (Eds.), Ecologia e conservação da Caatinga (p. 237–273). Recife: Edufpe.
Silvius, K. M., Bodmer, R. E., & Fragoso, J. M. V. (2004). People in nature: wildlife conservation in South and Central America. New York, NY: Columbia University Press.
Sodhi, N. S., Şekercioğlu, Ç. H., Barlow, J., & Robinson, S. K. (2011). Conservation of Tropical Birds. Hoboken, NJ: Wiley-Blackwell.
Souto, W. M. S., Barboza, R. R. D., Rocha, M. S. P., Alves, R. R. N., & Mourão, J. S. (2012). Animal-based medicines used in ethnoveterinary practices in the semi-arid region of Northeastern Brazil. Anais Da Academia Brasileira de Ciências, 84(3), 669–678. doi: 10.1590/S0001-37652012005000038.
Souza, J. B., & Alves, R. R. N. (2014). Hunting and wildlife use in an Atlantic Forest remnant of northeastern Brazil. Tropical Conservation Science, 7(1), 145–160. doi: 10.1177/194008291400700105
Tidemann, S., & Gosler, A. (2011). Ethno-ornithology: birds, indigenous peoples, cultures,and society. London, UK: Routledge.
Van Den Bergh, M. O. L., Kusters, K., & Dietz, A. J. T. (2013). Destructive attraction: factors that influence hunting pressure on the Blue Bird-of-paradise Paradisaea rudolphi. Bird Conservation International, 23(2), 221–231. doi: 10.1017/S0959270913000233
Van Vliet, N., Quiceno-Mesa, M. P., Cruz-Antia, D., Aquino, L. J. N., Moreno, J., & Nasi, R. (2014). The uncovered volumes of bushmeat commercialized in the Amazonian trifrontier between Colombia, Peru & Brazil. Ethnobiology and Conservation, 3(7), 1-11. doi: 10.15451/ec2014-11-3.7-1-11
Vieira, I. R., & Loiola, M. I. B. (2014). Percepção ambiental das artesãs que usam as folhas de carnaúba (Copernicia prunifera H. E. Moore, Arecaceae) na área de proteção ambiental Delta do Parnaíba, Piauí, Brasil. Sociedade & Natureza, 26(1), 63–76. doi: 10.1590/1982-451320140105
Von Ihering, R. (1935). La paloma, Zenaida auriculata, en el nordeste del Brasil. El Hornero – Revista de Ornitología Neotropical, 6(1), 37–47.
Notas de autor