Evidence-Based Complementary and Alternative Medicine

Evidence-Based Complementary and Alternative Medicine / 2012 / Article
Special Issue

Medical Ethnobiology and Ethnopharmacology in Latin America

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Research Article | Open Access

Volume 2012 |Article ID 679373 | 15 pages | https://doi.org/10.1155/2012/679373

Intracultural Variation in the Knowledge of Medicinal Plants in an Urban-Rural Community in the Atlantic Forest from Northeastern Brazil

Academic Editor: Ana H. Ladio
Received23 Jun 2011
Revised17 Aug 2011
Accepted23 Aug 2011
Published03 Nov 2011

Abstract

This study assessed the intracultural knowledge of the use of medicinal plants in an urban-rural community in an Atlantic forest fragment in northeastern Brazil. We examined the importance of native and exotic species and the effects of gender and age on that knowledge. We also compared data obtained from different groups of informants (local experts and general community). We conducted 194 interviews between June 2007 and January 2008, using the freelist technique and semistructured forms to collect ethnobotanical data. Information obtained from the community was compared with that from six local experts who participated in a survey in 2003. From a total of 209 ethnospecies, exotic and herbaceous plants presented higher richness. With respect to the number of citations, women and older informants were shown to know a higher number of medicinal plants. Comparing knowledge of local experts with that of the general community, we noted that experts know a similar wealth of plant families and therapeutic indications, but the community knows a greater species richness. These results indicate that local experts may provide useful information for studies that search for a quick diagnosis of the knowledge of a given community.

1. Introduction

In Brazil, the Atlantic Forest is one of the most biologically diverse ecosystems, responsible for harboring a large number of endemic species [1, 2]. It extends from Rio Grande do Norte to Rio Grande do Sul [3] and, given its location in the coastal area, is currently under strong pressure from real estate speculation. In addition, there are the pressures generated by timber extraction, the cycles of sugar cane, coffee, and gold, and, more recently, the expansion of farming and forestry with exotic species.

Human populations living in the surrounding areas of the Atlantic Forest play an important role in its exploitation as they often rely on forest resources for their subsistence and extract biological resources from it on a daily basis [4]. Understanding how these people use such resources is a task of great current interest, which may contribute to the discovery of products of economic interest and to the conservation of biological resources.

Thus, ethnobotanical studies can contribute to assessing how local knowledge is distributed among members of a community and the relationship between that knowledge and the increase of exotic species in the local repertoire of medicinal plants [57].

Common knowledge about plant resources, especially medicinal ones, is highly dynamic and subject to several influences, may vary according to gender, age, education level, income, roles that individuals play within the family, skills, and abilities [811], and may represent key elements of the knowledge of the diversity and richness of species [12].

Different social patterns have been reported to impact the knowledge of medicinal plants, emphasizing the need of studies that address such questions. For instance, Almeida et al. [13] did not observe any differences between the knowledge of men and women, whereas age and income were correlated with the number of citations for a given plant and its indication, suggesting that older people with a higher income had greater knowledge about such plant resources.

Thus, the goal of this study was to assess the intracultural knowledge of the use of medicinal plants in an urban-rural community in an Atlantic forest fragment in northeastern Brazil in order to document the importance of native and exotic species within the group of plants mentioned and the effects of gender and age on the knowledge of medicinal plants and to compare the quality of information gathered from different groups of informants (local experts versus general community).

2. Materials and Methods

2.1. Study Area

The study was conducted at Igarassu, located in the microregion of Itamaracá and the mesoregion of Recife, in Pernambuco state (7°50′20′′ S and 35°00′10′′ W; 20 m a.s.l.), 30 km from the state capital [1416]. The climate is tropical, hot, and humid, with autumn/winter rains (according to the classification of Köeppen). The average annual temperature is 27°C, and the average annual rainfall is approximately 2,000 mm [1416]. The municipality has a total area of 304.2 km2, with a population of 72,990 people (219.9 inhabitants/km2), 74.9% of which live in urban areas [14].

The predominant vegetation is composed of remnants of Atlantic forest, secondary forests, mangroves, palm trees, and areas of commercial and subsistence agriculture. There are ecological reserves in the city, such as the São José Plant Forest, with tall, dense vegetation, located on Transcanavieira Highway (PE-41) and with an area of 323.30 ha [17].

The community studied is known as “Três Ladeiras” and is located on the lands of the “São José Plant,” a sugar refinery. The “São José Plant” is surrounded by Atlantic forest fragments belonging to an ecological reserve [18]. The forest is part of the conservation area of the Botafogo River basin, in accordance with state law no. 9860, which since August 12, 1986, has been aimed at protecting the landscape, soil, and river basin [19]. The fragments occupy a total area of 210 ha [18]. The community lies 30 km north of the county seat and is located at the back of a large hill, whose extension contains three elevations that give the community its name. The district has 1,794 inhabitants, of which 1,077 live in urban areas and 687 in rural ones [20].

Most men from the community work at the plant although the number of people employed by the refinery oscillates during the year, increasing and decreasing according to season and periods of land preparation, planting, and harvesting [15]. It is not unusual to find among the residents of the community families with small fields that provide nutritional and/or economic support during periods when there is no work at the plant [15]. There is no sanitation, medical care takes place in a health clinic for minor health problems, and disease control is provided by health workers through weekly home visits. Patients who require extra care are relocated to hospitals in the county seat of Igarassu.

2.2. Data Collection

Ethnobotanical data were obtained through the freelist technique, followed by semistructured interviews [21]. The interviews were conducted with the senior member of the family, over 18 years old, present on the visit of the interviewer. Initially, we obtained a Term of Informed Consent from those willing to participate in the study in accordance with the legal and ethical aspects of Resolution 196/96 from the Ethics and Research Committee [22].

Because the community had a large number of residents, we sampled 51% of all households and conducted 194 interviews (140 women and 54 men) between June 2007 and January 2008. The age of informants ranged from 18 to 93 years. For the interviews, one main question was asked: “What medicinal plants do you know?”. In a second event, we gathered information on each species mentioned, the part of the plant used, the method of preparation, its indication and contraindication, as well as socioeconomic data from informants, such as gender, age, family income, and number of residents in the household. Ages were grouped into five different groups, ranging from 18 to over 68 years.

We used the data obtained in this study and in the work of Gazzaneo et al. [15] to compare the information obtained from the general community and local experts, respectively. The latter study was conducted in the same community in 2003 and was attended by six informants identified as “local experts,” given their more detailed knowledge on the use of medicinal plants [23]. This group of informants was composed of three men and three women, with ages ranging from 51 to 102 years. The data sampling performed by Gazzaneo et al. [15] was intentionally nonrandom and assumed that local experts provide more specific, high-quality information about medicinal plants. To select this group of informants, the authors used the “snowball” method [24]. Data were collected using semistructured interviews that gathered information related to the knowledge of medicinal plants.

2.3. Species Categorization and Indications Mentioned by Informants

All plants mentioned during interviews were identified and classified as either native or exotic species according to their biogeographical origin. We considered native species those endemic to the study region and also native to South America. Exotic species were considered to be those of extracontinental origin, cultivated in the region, and widely distributed, such as tropical invasive and cosmopolitan species.

To calculate the relative importance of species, all indications mentioned by the informants were grouped into 18 disease categories, according to the classification from the World Health Organization [25]: digestive, respiratory, gynecological/urinary, circulatory, nervous, sensory, motor, puerperium, cutaneous, scarring, poisoning, neoplasia, hematopoietic, nutritional, infectious/parasitic, sexual inappetence and antiabortion, and postpartum. Diseases not categorized by the aforementioned system were grouped into the category “undefined ailments and pains” by virtue of their symptoms and signs of multiple origins [26].

All species mentioned by informants, excluding those commercialized, were collected, identified, and deposited in the herbaria of Professor Geraldo Mariz (UFP), at the Federal University of Pernambuco, Professor Dárdano de Andrade Lima (IPA), at the Agricultural Research Company, and Professor Sérgio Tavares (HST), at the Federal Rural University of Pernambuco.

2.4. Data Analysis

We calculated the value of relative importance (RI) for all species [27] with the following formula: , where NBS is the number of body systems treated by a particular species (NBSS) divided by the total number of body systems treated by the most versatile species (NBSVS) and NP is the number of attributed properties of a particular species (NPS) divided by the total number of properties attributed to the most versatile species (NPVS).

The chi-squared adherence test was used to check for differences between the following factors: number of native versus exotic plants and number of plants observed in each life form (herb, shrub, and tree). We also compared the richness of exclusive species between different age groups, richness of families, total number of mentioned species, and number of exclusive species between local experts and the general community.

We used the Kruskal-Wallis nonparametric test to test for differences in the richness of ethnospecies and mentioned indications between men and women and between each age group and to check for differences between the relative importance of species mentioned by local experts and the general community.

We used Williams’ -test to compare the proportion of the number of native and exotic species (exclusive or not) mentioned by local experts and the general community.

The Spearman correlation test was applied to check for the relationship between the number of ethnospecies and the number of mentioned indications according to the age of the informants and to check for a relationship between relative importance (RI) of species mentioned by the general community and the RI calculated for local experts.

All statistical analyses were performed using the statistical package BioEstat 5.0 [28].

3. Results

3.1. Richness of Medicinal Plants Mentioned by Informants

In total, 209 ethno-species were mentioned during interviews; 151 were identified to the species level and 21 to the genus level only (Table 1). The plants were distributed in 74 families, and most families (66%) were represented by up to two species. The most represented families were Lamiaceae (10 spp.); Caesalpiniaceae and Curcubitaceae (8 spp.); Asteraceae, Euphorbiaceae, and Mimosaceae (5 spp.).


Family/scientific nameVernacular nameHabitOriginCitation numberRI 2005*RI 2008

Acanthaceae
Justicia pectoralis Jacq.ChambáHerbsNative210.330.37
Justicia sp.Anador251.00
Graptophyllum pictum (L.) Griff.MelacilinaHerbsExotic150.670.94

Amaranthaceae
Alternanthera brasiliana (L.) Kuntze.NovalginaHerbsExotic30.35
Pfaffia glomerata (Spreng.) PedersonAcônico/AcônitoHerbsExotic170.670.27

Anacardiaceae
Anacardium occidentale L.Cajueiro roxoTreeNative1130.331.24
Mangifera indica L.MangaTreeExotic110.830.62
Schinus terebinthifolius RaddiAroeiraTreeNative2191.171.60
Spondias purpurea L.SiriguelaTreeNative30.27

Annonaceae
Annona montana Macfad.AticumTreeNative130.830.61
Annona muricata L.GraviolaTreeExotic40.30
Annona squamosa L.PinhaTreeExotic10.12

Apiaceae
Daucus carota L.CenouraHerbsExotic10.12
Foeniculum vulgare Mill.EndroHerbsExotic120.74
Pimpinella anisum L.Erva doceHerbsExotic450.331.09

Apocynaceae
Catharanthus roseus L. G. Don.Boa noite brancaHerbsExotic30.27
Hancornia speciosa GomesMangabaTreeNative10.170.12

Arecaceae
Acrocomia aculeata (Jacq.) Lodd. ex Mart.MacaibaTreeNative300.170.76
Cocos nucifera L.Coco amareloTreeExotic70.170.39
Elaeis guineensis Jacq.DendezeiroTreeExotic20.170.24
Syagrus sp.Coco catoléTreeNative60.500.42

Asteraceae
Acanthospermum hispidum DC.Espinho de ciganoHerbsExotic480.670.76
Conyza bonariensis (L.) Cronq.Rabo de raposaHerbsExotic30.330.12
Helianthus annuus L.GirassolHerbsNative100.170.12
Matricaria chamomilla L.CamomilaHerbsExotic70.12
Pluchea sp.Mar de cravoHerbs10.12
Gymnanthemum amygdalinum (Delile) Sch.Bip. ex Walp.AlcachofraHerbsExotic500.330.83
Asteraceae 1Carqueja20.12

Begoniaceae
Begonia reniformis Dryand.CapebaShrubNative30.170.24

Bignoniaceae
Handroanthus impetiginosus (Mart. ex DC.) MattosPau daico roxoTreeNative80.670.54

Bombacaceae
Chorisia sp.BarrigudaTreeNative10.12

Boraginaceae
Heliotropium angiospermum MurrayCrista de galoHerbsExotic10.12
Heliotropium indicum L.FedegosoHerbsExotic30.500.35

Brassicaceae
Nasturtium officinale R. Br.AgriãoHerbsExotic480.830.53

Bromeliaceae
Ananas comosus (L.) Merr.AbacaxiHerbsNative140.39
Tillandsia usneoides (L.) L.SalambaiaHerbsNative20.170.24

Burseraceae
Protium heptaphyllum (Aubl.) MarchandAmesclaTreeNative11.000.12

Cactaceae
Cereus jamacaru DC.CardeiroTreeNative50.12

Caesalpiniaceae
Bauhinia forficata LinkPata de vacaTreeNative90.30
Caesalpinia echinata Lam.Pau brasilTreeNative10.12
Caesalpinia ferrea Mart. ex Tul.JucáTreeNative110.500.27
Copaifera sp.Pau dóleoTree10.170.12
Hymenaea martiana HayneJatobáTreeNative271.331.20
Senna alata (L.) Roxb.Café beirãoShrubExotic10.12
Senna occidentalis (L.) Link.Manjirioba/Mata pastoHerbsExotic240.170.76
Poincianella pyramidalis (Tul.) L. P. QueirozCatingueiraTreeNative10.12

Capparaceae
Cleome spinosa Jacq.MussambêShrubExotic110.170.30

Caprifoliaceae
Sambucus nigra L.Flor de sabugo/SabugueiroTreeExotic330.500.57

Caricaceae
Carica papaya L.MamãoTreeNative70.330.46

Caryophyllaceae
Dianthus caryophyllus L.Cravo brancoHerbsExotic40.27

Cecropiaceae
Cecropia palmata Willd.Embauba brancaTreeNative60.330.42

Chenopodiaceae
Beta vulgaris L.BeterrabaHerbsExotic80.34
Chenopodium ambrosioides L.Mastruz/MentruzHerbsExotic850.670.68

Chrysobalanaceae
Licania sp.Oiti/Oiticica20.24
Chrysobalanaceae 1Oiticoró10.12

Clusiaceae
Vismia guianensis (Aubl.) Pers.LacreTreeNative120.330.42

Combretaceae
Buchenavia sp.Imbiriba40.330.15
Terminalia catappa L.Coração de negroTreeExotic20.58

Convolvulaceae
Ipomoea asarifolia (Ders.) R. et SchSalsaHerbsExotic10.170.15
Operculina alata (Ham.) Urb.Batata de purgaHerbsNative10.500.12
Convolvulaceae 1Acanfó/Acafú100.330.34
Convolvulaceae 2Sassá10.12

Crassulaceae
Kalanchoe laciniata (L.) DC.Corona brancaHerbsExotic170.81
Kalanchoe sp.Corona roxa60.51

Cucurbitaceae
Citrullus vulgaris Schard.MelânciaHerbsExotic10.12
Cucumis anguria L.MaxixeHerbsExotic10.12
Cucumis melo L.MelãoHerbsExotic10.12
Cucumis sativus L.PepinoHerbsExotic20.24
Curcubita pepo L.JerimumHerbsExotic80.24
Luffa operculata L. Cong.CabacinhaHerbsNative10.170.12
Momordica charantia L.Melão de são caetanoHerbsExotic10.12
Sechium edule (Jacq.) Sw.ChuchuHerbsExotic200.170.27

Equisetaceae
Equisetum sp.CavalinhaHerbs10.12

Euphorbiaceae
Cnidosculus urens (L.) ArthurUrtiga brancaHerbsNative250.500.68
Euphorbia tirucalli L.AvelozShrubExotic10.12
Jatropha gossypiifolia L.Pinhão roxoShrubExotic50.35
Jatropha mollissima (Pohl.) Baill.Pinhão brancoShrubNative20.24
Manihot esculenta CrantzMacacheira/RoçaHerbsNative10.12
Phyllanthus niruri L.Quebra pedraHerbsExotic130.170.46
Ricinus communis L.Carrapateira/MamonaShrubExotic50.27

Fabaceae
Bowdichia virgilioides KunthSucupiraTreeNative50.500.39
Vicia faba L.FavaHerbsExotic10.12
Zornia diphylla (L.) Pers.UrinanaHerbsNative30.170.15

Flacourtiaceae
Flacourtiaceae 1Imbira branca20.12

Heliconiaceae
Heliconia psittacorum L. f.PaquiviraHerbsNative10.12

Illiaceae
Illicium verum Hook. f.Anil estreladoTreeExotic90.73

Iridaceae
Crocus sp.AçafrãoHerbs10.330.12
Eleutherine bulbosa (Mill.) Urb.Alho do matoHerbsNative30.670.15

Lamiaceae
Aeollanthus suaveolens Mart. ex Spreng.MacassáHerbsExotic321.331.13
Mentha piperita L.Hortelã miúdaHerbsExotic1410.832.00
Mentha pulegium L.Hortelã pastilha/H. vickHerbsExotic340.171.07
Ocimum basilicum L.Manjericão/Manjericão são joséHerbsExotic500.501.16
Ocimum basilicum var. minimum (Willd.) Benth.Manjericão miúdoHerbsExotic50.170.35
Ocimum campechianum Mill.Alfavaca de cabocloHerbsNative140.69
Ocimum gratissimum L.Louro falso/L. caseiro/ Hortelã fernando/H. são severinoHerbsExotic40.170.24
Plectranthus amboinicus (Lour.) Spreng.Hortelã graúda/H. gorda/H. bahiaHerbsExotic1550.831.22
Plectranthus barbatus AndrewsBoldo caseiro/Boldo falso/Hortelã cabocloHerbsExotic170.500.84
Rosmarinus officinalis L.AlecrimHerbsExotic110.170.96
Lamiaceae 1AlfazemaHerbs10.12
Lamiaceae 2Alfazema de cabocloHerbs10.12
Lamiaceae 3Veiga mortaHerbs530.500.84

Lauraceae
Nectandra cuspidata Ness & Mart.CanelaTreeNative710.95
Persea americana Mill.AbacateTreeExotic150.830.62

Liliaceae
Allium cepa L.CebolaHerbsExotic120.670.34
Allium sativum L.AlhoHerbsExotic190.330.56
Aloe vera (L.) Berm.f.Baborsa/Erva babosaHerbsExotic320.831.13

Loranthaceae
Loranthaceae 1Cipó estanca sangue10.330.12

Malpighiaceae
Byrsonima sericea DC.MuriciTreeNative10.12
Malpighia glabra L.AcerolaTreeExotic100.51

Malvaceae
Gossypium barbadense L.AlgodãoShrubExotic20.500.20
Uerna lobata L.Malva rosaHerbsNative110.330.51

Meliaceae
Cedrela odorata L.CedroTreeNative10.12

Mimosaceae
Acacia sp.EspinheiroTree30.12
Anadenanthera colubrina (Vell.) Brenan.AngicoTreeNative30.24
Inga bahiensis Benth.Inga porcoTreeNative10.12
Mimosa tenuiflora (Willd.) Poir.Jurema pretaTreeNative20.12
Piptadenia stipulacea (Benth.) Ducke.Jurema brancaTreeNative10.12
Pithecellobium cochliocarpum (Gomez) Macbr.BabatenomTreeNative1831.831.14
Pithecellobium saman var. acutifolium Benth.Budão de velhoTreeNative20.24

Monimiaceae
Peumus boldus Mol.Boldo do chileHerbsExotic440.73

Moraceae
Artocarpus communis J.R. Forst. & G. Forst.Fruta pãoTreeExotic30.35
Artocarpus integrifolia L. f.JacaTreeExotic20.24
Dorstenia sp.Conta erva10.830.12

Musaceae
Musa paradisiaca L.BananeiraTreeExotic190.330.73

Myrtaceae
Eucalyptus citriodora Hook.EucaliptoTreeExotic70.170.24
Eugenia uniflora L.PitangaTreeNative580.170.59
Psidium guajava L.GoiabaTreeNative510.170.24
Psidium guineense Sw.AraçaShrubNative50.170.12
Syzygium aromaticum (L.) Merr. & L.M. PerryCravo do reinoTreeExotic50.59
Syrygium jambolanum (Lam.) DC.Azeitona pretaTreeExotic140.170.69

Nyctaginaceae
Boerhavia diffusa L.Pega pintoHerbsExotic221.170.83
Guapira sp.João moleTree30.24

Olacaceae
Ximenia americana L.AmeixaTreeNative10.170.12

Oxalidaceae
Averrhoa carambola L.CarambolaTreeExotic170.830.30

Papaveraceae
Argemone mexicana L.Cardo santoHerbsExotic70.500.24

Passifloraceae
Passiflora edulis Sims.MaracujáShrubNative120.170.49

Pedaliaceae
Sesamum orientale L.Gergelim preto/GigilimHerbsExotic40.170.24

Phytolacaceae
Petiveria alliacea L.TimpiHerbsNative70.670.54

Piperaceae
Peperomia pellucida H.B.K.Lingua de sapoHerbsNative50.39
Piper nigrum L.Pimenta do reinoShrubExotic20.24

Poaceae
Cymbopogon citratus (DC.) StapfCapim santoHerbsExotic1330.501.47
Imperata brasiliensis Trin.SapéHerbsNative50.15
Phalaris canariensis L.AlpisteHerbsExotic40.170.24
Zea mays L.MilhoHerbsExotic20.12

Polygalaceae
Polygala sp.Esquentado10.12

Punicaceae
Punica granatum L.RomãTreeExotic140.49

Rhamnaceae
Zizyphus joazeiro Mart.JuáTreeNative220.830.76

Rosaceae
Pyrus malus L.MaçãTreeExotic10.12
Rosa sp.1Rosa amélia10.12
Rosa sp.2Rosa branca70.330.62

Rubiaceae
Borreria verticillata L. G. Mey.Vassoura de botãoHerbsExotic471.171.51
Genipa americana L.JenipapoTreeNative530.64
Uncaria tomentosa (Willd. ex Roem. & Schult.) DC.Unha de gatoTreeNative10.12

Rutaceae
Citrus limetta RissoLimaTreeExotic10.12
Citrus limonia OsbeckLimãoTreeExotic140.57
Citrus sinensis (L.) OsbeckLaranjaTreeExotic440.830.93
Ruta graveolens L.ArrudaHerbsExotic750.831.08

Sapindaceae
Cardiospermum halicacabum L.Cipó de vaqueiroShrubNative100.330.24
Cupania sp.Cabotam10.330.12
Serjania sp.Cipó cururu20.12

Sapotaceae
Achras zapota L.SapotiTreeExotic10.12
Sideroxylon obtusifolium (Roem. & Schult.) T.D. Penn.QuixabaTreeNative271.14

Smilacaceae
Smilax rotundifolia L.Cipó japecangaHerbsNative60.170.12

Solanaceae
Capsicum frutescens L.PimentaShrubNative30.24
Nicotiana tabacum L.FumoHerbsNative10.12
Solanum americanum Mill.Avamoura/Erva mouraHerbsExotic50.170.30
Solanum paniculatum L.JurubebaShrubExotic41.000.35

Sterculiaceae
Guazuma ulmifolia L.MutambaTreeNative70.24

Theacaea
Camellia sinensis (L.) KuntzeChá pretoShrubExotic40.20

Turneracea
Turnera ulmifolia L.XananaHerbsExotic10.170.12

Verbenaceae
Lantana camara L.ChumbinhoShrubNative50.330.19
Lippia alba (Mill.) N.E.Br.Cidreira/Erva cidreiraHerbsExotic940.671.86
Stachytarpheta elatior Schrad. ex SchultMocotóHerbsNative40.670.12
Vitex agnus-castus L.LiambaTreeExotic20.170.24

Violaceae
Hybanthus sp.Pepaconha70.51

Vitaceae
Cissus verticillata (L.) Nicolson & C.E. JarvisInsulinaShrubNative50.170.12
Leea sp.Café30.27
Vitis vinifera L.UvaShrubExotic10.12

Zingiberaceae
Alpinia zerumbet (Pers.) Burt. ex R. M. SmithColônia/ColonhaHerbsExotic1901.670.91
Costus sp.Cana de macaco270.84
Zingiber officinalis Rosc.Gengibre vermelhoHerbsExotic10.12

Unidentified
Unidentified 1Abre caminho20.12
Unidentified 2Açafroa1
Unidentified 3Boca torta10.12
Unidentified 4Bugre20.12
Unidentified 5Cafofa10.12
Unidentified 6Canela de viado10.12
Unidentified 7Chumbinho branco10.12
Unidentified 8Cipó de boi20.24
Unidentified 9Imbira vermelha20.12
Unidentified 10Malicia branca20.24
Unidentified 11Malicia boi/M. fina40.15
Unidentified 12Malva ferro10.12
Unidentified 13Moça10.12
Unidentified 14Pé de galinha/Papo de peru10.12
Unidentified 15Pega rapaz10.12
Unidentified 16Perpetua branca10.12
Unidentified 17Piripiri10.12
Unidentified 18Piriquiti10.12
Unidentified 19Quebra faca50.27
Unidentified 20Quentão10.12
Unidentified 21Rasteira10.12
Unidentified 22Rasteirinho10.12
Unidentified 23Salsa caroba10.12
Unidentified 24Sete casco10.12
Unidentified 25Tatajuba10.12

*(—) denotes the absence of the species on the list of Gazzaneo et al. [15].
RI 2005: relative importance calculated from information given by local experts; RI 2008: relative Importance calculated from information given by the general community.

With respect to the origin of the identified species, we observed that 89 were exotic and 62 were native (Figure 1), and the difference was statistically significant ( ; ). That result indicates that informants knew more exotic plants that could be used for medicinal purposes. With respect to the life form of plants, there was a predominance of herbs (74), followed by trees (59) and shrubs (18) (Figure 1), but we only observed statistical differences when we compared the richness of shrubs with that of herbs ( ; ) and trees ( ; ). The number of herbs and trees was not significantly different ( ; ), indicating that the richness of herbs and trees was similar in the pool of plants mentioned by informants. However, when considering the distribution of species according to their origin, we observed a different pattern: for exotic plants, there was a higher number of herbaceous plants compared to the other two life forms (shrubs: , ; trees: , ), whereas, for native plants, there was a higher number of trees (herbs: , ; shrubs: , ).

The most mentioned species were Schinus terebinthifolius Raddi (aroeira-219 citations), Alpinia zerumbet (Pers.) B. L. Burtt & R. M. Sm. (colônia-190 citations), Pithecellobium cochliocarpum (Gomez) Macbr. (babatenon-183), Plectranthus amboinicus (Lour.) Spreng (hortelã graúda-155), Mentha piperita L. (hortelã miúda-141), and Cymbopogon citratus (DC.) Stapf (capim santo-133) (Table 1). Except for S. terebinthifolius and P. cochliocarpum, all these plants are exotic, emphasizing the importance of exotic plants to the knowledge of medicinal plants in the region.

3.2. Influence of Gender and Age on the Knowledge of Medicinal Plants

There were significant differences in the knowledge of medicinal plants according to gender, with women knowing a higher richness of ethno-species ( ; ) and indications ( ; ). They mentioned a total of 166 ethno-species, with a mean number of citations per person, and a total of 146 indications, with a mean of citations per person, whereas men mentioned 136 ethno-species and 93 indications, with a mean of and citations per person, respectively.

The number of plants and indications mentioned by each informant correlated with their age ( , ; , , resp.). However, when we compared the average number of ethnospecies and indications in each age group, we observed different patterns (Table 2). The number of known plants only varied in informants from the 18–28-year-old age group, suggesting that the richness of known plants was smaller in younger participants, which may reflect the limited experience and contact of young informants with plant resources from the region. Although informants aged 49–58 years old had greater knowledge of medicinal plants in the region, they were only significantly different from younger informants (Table 2). With respect to the number of indications mentioned in each age group, we observed a similar pattern to the previous one, with younger informants (18–28 yrs.) knowing a smaller variety of indications. However, the knowledge of informants was significantly higher for the age groups 49–58 years old and older than in other age groups.


Age groupsNIGeneral average number of ethno-speciesGeneral average number of indicationsNMINFI Average number of cited ethno-species Average number of cited indicationsTotal diversity of cited speciesNumber of exclusive species
MaleFemaleMaleFemale

18–28438.8 ± 6a6.3 ± 3.6a8355.37 ± 1.9a9.57 ± 6.4a4 ± 1.2a6.83 ± 3.8a8510
29–384411.66 ± 6.2b8.84 ± 4.6b8367.6 ± 3.7ac12.55 ± 6.3b5.75 ± 2ac9.53 ± 4.8b10311
39–484111.98 ± 6.6b9 ± 4.9b12298.83 ± 4.3ad13.28 ± 7b7.67 ± 4.5ac9.66 ± 5.1b9912
49–582816.39 ± 11b12.79 ± 7.7c72111.71 ± 9.6bcd17.95 ± 11.3b9.14 ± 6.9bc14 ± 7.8c12019
59–682414.58 ± 8.8b10.7 ± 6.1c141012.93 ± 9.4bcd16.9 ± 7.8b9.14 ± 6.3bc12.9 ± 5.2bcd11219
>6914 59 877

*Equal letters in the same column indicate a lack of statistical differences using the Kruskal-Wallis test ( ). NI: number of informants; NMI: number of male informants; NFI: number of female informants.

When we analyzed the influence of gender and age on the distribution of knowledge, we observed a few patterns that often differed from the data presented by the general community. Younger women (18–28 yrs.) also had less knowledge of the richness of medicinal species, while, in other age groups, knowledge was homogeneous. For women, we observed the formation of two groups regarding the number of indications: one group consisting of the three younger groups, with a lower number of indications, and the other consisting of older age groups, with a higher number of indications.

For men, knowledge of plant richness and indications showed a different pattern. The knowledge of informants in the 18–48-year-old age groups did not present any statistical differences. That difference only appeared in the age groups 49–58 years old and older, indicating an increase in the number of species known and the variety of indications occurring only in older age groups, whereas for women it was also observed in younger age groups.

We observed a continuous increase in the number of ethno-species mentioned with an increase in age, for both men and women, when total plant richness was considered (Figure 2), up to the age group with the highest richness of plants mentioned. In subsequent age groups, plant richness started to decrease. Among women, the 49–58-year-old age group had the greatest knowledge of plants (109 ethno-species), whereas for men the greatest knowledge of plants was observed in an older class (59–68 yrs.). These results indicate that, in the community of Three Hills, the commitment of women to family care compels them to know, from an early age, a large number of plants with medicinal purposes.

Following the age groups with a higher number of plants, there was a decrease in plant richness in older groups, possibly related to memory loss, which is common among older people. We did not observe the same pattern when the mean number of plants mentioned by informants was analyzed, as previously noted (Table 2). In this case, people still mentioned a high number of citations, even in the oldest age group (>69 yrs.).

Exclusive species were mentioned in all age groups (Table 2), with a total richness of 78 exclusive species distributed in the six age groups. The 49–58- and 59–68-year-old age groups stand out for their higher richness, although there were no statistical differences in the number of exclusive species between age groups ( ; ), indicating that, in every age group, informants had a repertoire of exclusive plants that was not shared by people from other age groups.

3.3. Analysis of the Knowledge of Medicinal Plants between Local Experts and the General Community

Data obtained from the general community presented a higher richness of plant families and medicinal species when compared with data obtained from local experts. The difference was highly significant for total species richness ( , ) and exclusive species richness ( , ) but was not significantly different for the richness of plant families ( , , Figure 3). The results indicate that the knowledge of local experts managed to represent the richness of useful plant families cited by the general community but not the total number of species (Table 3). However, the most species (84.2%) mentioned by at least 20 informants from the general community were also mentioned by local experts. This result indicates that expert informants mentioned medicinal plant species that are better known among other members of the community.


Family/scientific nameVernacular nameHabitOriginRI

Asteraceae
Egletes viscosa (L.) Less.MacelaHerbsExotic0.17
Tagetes sp.Cravo de defuntoHerbs0.17

Caesalpiniaceae
Senna obtusifolia (L.) H.S. Irwin & BarnbeyMata pastoHerbsExotic0.17
Tamarindus indica L.TamarindoTreeExotic0.17

Caprifoliaceae
Sambucus australis Cham. & SchlechtFlor de sabugoTreeExotic0.50

Clusiaceae
Symphonia sp.BulandiHerbs0.17

Euphorbiaceae
Croton sp.MarmeleiroShrubNative0.17
Euphorbia thymifoliaL.Pé de pomboHerbsNative0.67

Loranthaceae
Phthirusa pyrifolia (H.B.K.) Eichl.Esterco de passarinhoHerbsNative0.50

Malvaceae
Malva sp.Malva brancaHerbs0.17

Poaceae
Brachiaria mutica (Forsk.) StapfCapim de plantaHerbsExotic0.33
Dendrocalamus giganteus MunroBambuTreeExotic0.17
Saccharum officinarum L.CanaHerbsExotic0.17

Rhizophoraceae
Rhizophora mangle L.MangueTreeNative0.33

Rubiaceae
Cephaelis ipecacuanha (Brot.) A. Rich.PapeconhaHerbsNative0.50

Rutaceae
Pilocarpus sp.Jaborandi0.33

Sapotaceae
Pradosia sp.Burinhê0.33

Scrophulariaceae
Scoparia dulcis L.VassourinhaHerbsExotic0.17

RI: relative importance value.

The numbers of exotic and native species mentioned by local experts and that by the general community were not significantly different according to Williams’ -test ( , ). Among exclusive species, we also did not observe any significant differences between native and exotic plants ( , ), suggesting that local experts and the general community presented a similar citation repertoire of native and exotic species.

There was no significant difference between the relative importance (RI) of species mentioned by local experts and that by general community ( , ). We observed a significant correlation between local experts and the general community in the number of indications per species according to the Spearman correlation test ( , ). This result suggests that local experts and the general community provided similar information regarding the indication of medicinal plant species. Among the ten species with higher RI mentioned by local experts and the general community, the species Borreria verticillata L. G. Mey., Hymenaea martiana Hayne, Mentha piperita L., Pithecellobium cochliocarpum (Gomez) Macbr., and Schinus terebinthifolius Raddi occurred in both studies. These results show that using local experts to provide information on the indications of medicinal plants was useful in the given context. However, the same was not observed for data on species richness. Thus, we recommend engaging the whole community to gather such data. Such precaution may prevent a large number of known species from being neglected, as in our study.

4. Discussion

4.1. Richness of Medicinal Plants Mentioned by Informants

The study showed high diversity in the knowledge of medicinal plants, with significant results for species prescribed for basic health care. The acceptance of folk medicine and the limited access to public healthcare services in the community may be factors contributing to the knowledge of medicinal species in local medical practices.

A few plant families prominent in this study, such as Lamiaceae and Asteraceae, are reported as very diverse taxonomic groups in the literature. Their high diversity probably reflects a greater amount of bioactive compounds [29], which may explain their prominence in this study and in similar ones in other regions [30, 31].

Most medicinal plants used in the study area are exotic herbs that usually grow in anthropogenic areas, such as agricultural fields, gardens, and roads. Other studies performed in forest environments in different regions have shown that traditional communities select anthropogenic areas as important resource sources [3236]. The frequent citation of herbs in the community of “Três Ladeiras” may be a consequence of the importance of this life form in anthropogenic areas, also due to the presence of strong bioactive compounds. In a study conducted in the same community, Gazzaneo et al. [15] also reported that more of the medicinal plants used by experts were herbs, collected mainly in the backyards of homes and small farms.

According to Voeks [37], weeds are often abundant in easily accessible places and rich in bioactive compounds, and as a result they are widely represented in tropical medicinal floras.

4.2. Influence of Gender and Age on the Knowledge of Medicinal Plants

Women had greater knowledge of medicinal plants when compared to men in the community studied. That result was probably due to women being the caregivers for their families, a trend also observed in other studies [5, 3840]. This scenario may also reflect the different activities performed by men and women in the community because the latter must dedicate themselves to their homes and families, which help them assimilate the knowledge they will need to keep their homes healthy at an earlier age. We should add that most species from the list of mentioned plants were exotic and herbaceous plants that are found in places women are more familiar with, such as backyards.

The study showed that young informants had less knowledge of medicinal plants when compared to older ones, which can be attributed to a lack of interest in learning and practicing such knowledge in younger generations, who are increasingly influenced by modernization. Several studies have reported similar results [38, 4145]. It is also important to notice that older people are more experienced and have had greater contact with plant resources and time to exchange knowledge with other informants from the region. Moreover, older people are more often affected often by various illnesses, which may help to increase their repertoire of plants and indications. In addition, they are responsible for preparing home remedies for themselves and for younger people, favoring the retention of knowledge and prompting younger individuals to use the plant resource without necessarily having knowledge of the remedy or its preparation.

4.3. Analysis of the Knowledge of Medicinal Plants between Local Experts and the General Community

This research showed that studies focused on experts can generate useful information, with a satisfactory level of reliability. But these are eminently suitable for quick diagnosis about the knowledge and use of medicinal plants in a community. That approach has the advantage of minimizing costs and time when collecting ethnobotanical data in the community surveyed. However, studies aiming to gather such information in greater detail should ideally engage other members of the community. That may prevent a large number of known species from being neglected. Vandebroek [46] reports that the careful selection of informants is a key task of the ethnobiologist and cannot be a simple step. The author suggests that, for a scientifically rigorous research, should be involved as many participants as possible, but if time is really a limiting factor, it is necessary to select key informants who have a high degree of knowledge about plants in the region as well as a high level of consensus with others.

Within this scenario, the association between both groups of informants is also possible [4547]. In fact, the information gathered from key informants (experts) in those studies helped prepare semistructured forms and consensus analyses among informants. In some cases, local experts are used as facilitators for data collection, accompanying the researcher during interviews with other members of the community. These studies serve as examples of the advantages and limitations of different informant profiles and emphasize the importance of clearly establishing the goals the researcher hopes to achieve to best engage the most appropriate informants.

It should be noted, additionally, that there was a five-year interval between the data obtained from local experts and the general community. The influence of such a gap could not be measured or controlled, given the sampling design of each study and the dynamic character of human knowledge, and this limitation restricts the possibility of extrapolating the considerations discussed here. Moreover, we could not completely rule out the possibility that the so-called local expert informants have been added to the sample of the present study.

Acknowledgments

The authors thank the community of Três Ladeiras for the participation and Vanduís Valdino for fieldwork help. They also thank the contribution of the project “Sustainability of remnants of the Atlantic rainforest in Pernambuco and its implications for conservation and local development,” a Brazilian-German scientific cooperation within the program “Science and Technology for the Atlantic Rainforest” funded by CNPq (590039/2006-7) and BMBF (01 LB 0203 A1). The authors’ gratitude also goes to CNPq for the financial aid (Edital Universal) and productivity grant for research awarded to U. P. de Albuquerque and CAPES to CF. C. B. R. de Almeida.

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Copyright © 2012 Cecília de Fátima Castelo Branco Rangel de Almeida et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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