Evidence-Based Complementary and Alternative Medicine

Evidence-Based Complementary and Alternative Medicine / 2012 / Article
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The European Heritage of Folk Medicines and Medicinal Foods: Its Contribution to the CAMs of Tomorrow

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Research Article | Open Access

Volume 2012 |Article ID 896295 | https://doi.org/10.1155/2012/896295

Esperança Carrió, Montse Rigat, Teresa Garnatje, Marina Mayans, Montse Parada, Joan Vallès, "Plant Ethnoveterinary Practices in Two Pyrenean Territories of Catalonia (Iberian Peninsula) and in Two Areas of the Balearic Islands and Comparison with Ethnobotanical Uses in Human Medicine", Evidence-Based Complementary and Alternative Medicine, vol. 2012, Article ID 896295, 22 pages, 2012. https://doi.org/10.1155/2012/896295

Plant Ethnoveterinary Practices in Two Pyrenean Territories of Catalonia (Iberian Peninsula) and in Two Areas of the Balearic Islands and Comparison with Ethnobotanical Uses in Human Medicine

Academic Editor: Manuel Pardo-de-Santayana
Received01 Mar 2012
Accepted15 Apr 2012
Published08 Jul 2012

Abstract

This paper presents the results of an ethnobotanical study centred in veterinarian uses in two Catalan Pyrenean regions (Alt Empordà -AE- and High River Ter Valley -AT-, Iberian peninsula) and two Balearic Islands areas (Formentera -FO- and northeastern Mallorca -MA-). In the areas studied, 97 plant species have been claimed to be useful for veterinary purposes. A total of 306 veterinary use reports have been gathered and analysed. The ten most reported plants are Tanacetum parthenium (24 use reports), Parietaria officinalis (15), Ranunculus parnassifolius (14), Meum athamanticum (13), Olea europaea (13), Quercus ilex (12), Ruta chalepensis (12), Sambucus nigra (10) and Thymus vulgaris (10). According to comprehensive reviews, a high number of novelties for plant ethnoveterinary are contributed: 34 species and one subspecies, 11 genera, and three families have not been reported in previous works in this field, and 21 species had only been mentioned once. Several ethnoveterinary uses are coincidental with those in human medicine. Although ethnoveterinary practices are less relevant than in the past in the territories considered, as in all industrialised countries, the knowledge on plant properties and applications is still rich and constitutes a large pool of evidence for phytotherapy, both in domestic animals and humans.

1. Introduction

Community animals have always been and continue to be intimately linked to human societies’ life. Domesticated (livestock, horses, poultry, other cage food animals such as rabbits, and most pets) and wild animal species (some occasionally captured pets, e.g., certain cage birds) live together with people, who obtain benefits and, at the same time, take care of them. Traditional veterinary practices are documented from as long as 14,000 years ago [1], being at least as ancient as animal domestication [2]. Given the kind of animals dealt with, the rural environment is where such practices (often including healing) are most extended, but pets and other small domestic animals are also quite present in urban areas. This is why ethnoveterinary knowledge is currently in use not only in developing countries, where often no other resources are available, but in developed ones as well, where it constitutes a very valuable complement and/or alternative to the so-called Western veterinary medicine [3].

Ethnoveterinary knowledge constitutes a relevant part of ethnobiological knowledge [1]. Data on veterinary plant uses are universally and significantly present in every general ethnobotanical prospection, and even more in those, very frequently, biased to ethnopharmacological aspects. This can be illustrated with a few -out of the very abundant- case examples of monographic ethnobotanical studies in different continents including diverse geographical or thematic approaches and different kinds of societies as regards industrialization level [49].

Apart from ethnoveterinary data appearing in general ethnobiological works, a considerable effort has been made to address this subject specifically. All angles of animal health care have been studied, among which those with an ethnographic focus are very relevant. A recent bibliographic compilation [3] provides data from 118 countries all over the world regarding 200 health troubles in 25 livestock species. A great number of papers on ethnoveterinary appear both in ethnobiological and veterinary journals, indicating contemporary interest of the subject in distinct fields. This means that the folk knowledge on animal health problems and the most frequent plant-derived remedies used to treat them are not merely an affair of past times but continue to play an important role in alternative or complementary medicine. To exemplify this we will quote again only an extremely reduced part of the very numerous sources specifically devoted to ethnoveterinary uses and practices, also covering different parts of the world, some of them very general and others focused on a single animal [1026]. Strictly medical veterinary uses are often complemented with animal feed. In fact, a relatively new return to natural detected in the field of ethnoveterinary (not only referring to traditional ancestral plant use but also to modern uninformed access to plant products as well) has made the border between feed and medicine rather diffuse when addressing health care in animals [15]. In any case, the advanced state of art of ethnoveterinary has already made possible a synthetic work aiming to constitute a worldwide inventory of botanicals for animal health including 451 plant species [27]. All the above-cited general works [49] contain, in addition to veterinary ones, data on human medicinal uses, and some of the ethnoveterinary-centred ones also establish the comparison between medicinal uses addressed to humans and animals in the same sociogeographical group [23].

Ethnobotanical studies in Europe -most of them, as already stated, containing ethnoveterinary data- have been and still are abundant ([28] and references therein). Among these, in southern Europe, and in particular in Iberian territories, dealt with in the present paper, specific ethnoveterinary work is not at all scarce, especially in recent times [16, 2935]. Nevertheless, in Catalonia only two works particularly deal with ethnoveterinary [31, 36], whereas no studies on this subject have been published to date concerning the Balearic Islands.

The efforts made over the last years to inventory the ethnoveterinarian heritage respond to the fact that industrialisation and rural depopulation have diminished the dependence of people on animals and caused a decrease in traditional animal healing [1] and that the ethnoveterinary knowledge is weak, since it depends exclusively on oral transmission [19]. This weakness is particularly worrying in developed countries, where much more industrial medicine is available and easy to use. Ethnobotanical studies focused on medicinal and on food plants have been previously published from the two Catalan regions considered ([3739] and references therein), but only very scarce ethnobotanical information is available from the islands of Mallorca and Formentera ([40, 41] and references therein), and ethnoveterinary medicine has not been addressed at all, to date, in any of those territories. Consequent with this situation, the aims of the present work are (1) to inventory plant ethnoveterinary resources in several Catalan and Balearic regions in order to compare the data obtained in insular and continental territories; (2) to evaluate the degree of coincidence of veterinary and human medicinal plant uses in the zones considered; (3) to assess consensus and reliability of these uses and so the vitality of complementary and alternative medicinal practices and their real incidence in the healthcare system.

2. Methods

2.1. Study Areas

The territories studied are located in southwestern Europe (Figure 1) and grouped in two close but distinct geographical areas as follows. On the one hand, two regions in the eastern Pyrenees (Catalonia, Iberian peninsula): the district (in Catalan “comarca”) of Alt Empordà (AE), in the foothills of the Pyrenees, and the high mountain area of the High River Ter Valley (AT). On the other hand, two regions in the Balearic Islands: the Artà peninsula area (northeastern) in Mallorca (MA) and Formentera (FO). All these territories share political administration (Spanish) and language (Catalan) and have a common ethnographic and cultural background, with the logical regional nuances.

The Alt Empordà territory comprises 1,358 km2 and has around 138,000 inhabitants living in 68 municipalities. The climate is mainly coastal Mediterranean, with a global mean rainfall of 550–750 mm per year and an annual mean temperature of 15.2°C (data from the Catalan Meteorological Service [42]). The most well-known and deep-rooted meteorological phenomenon is a northwesterly wind called the tramuntana, responsible for some natural effects, such as some wind-adapted vegetation forms and the desiccation of crops. The district contains an uneven distribution of distinct biogeographical regions—two predominantly Mediterranean ones and also the Eurosiberian in certain mountainous areas [43]. Economically, this area has evolved from an initial agriculture and livestock raising and subsequent industrial forestry exploitation (especially cork) to the more recent tourism and real-estate boom, stronger on the seaside Costa Brava. The High River Ter Valley occupies 294 km2 within the Ripollès district. To the North, the valley is limited by peaks that reach almost 2,900 m. The weather is typical of high mountain areas, with cold winters (mean temperature around 3°C) and a mean annual precipitation of 1,284 mm (data corresponding to 2003, Birba, pers. comm.), although the proximity of the Mediterranean Sea softens the climatic conditions. The predominant vegetation belts are the alpine and subalpine [43, 44]. This valley is inhabited by 4,526 people (municipal census, 2004), distributed in 18 population centres belonging to six municipalities. Some of them have suffered an important population decrease, although in recent years houses have been gradually reoccupied as second residences. Agriculture is not very relevant, given its climatic conditions and uneven territory, but many farms and houses within the villages have their own homegardens for private consumption.

Formentera is the smallest of the four inhabited Balearic Islands. It occupies 82 km2 and has 9,147 inhabitants (data from 2008) [45] living in nine population centres belonging to one municipality. Its maximum altitude is 195 m, and the climate is Mediterranean with an arid tendency, with an annual mean temperature of 18.6°C and an annual mean rainfall of 370 mm [46]. The main vegetation landscape on this island is the coastal Mediterranean one [43]. Agriculture, timber exploitation, fishing, and salt production have been relevant activities on the island, but nowadays tourism is the most important economic activity. The prospected area in Mallorca is the Artà peninsula, covering the highest part of the Eastern Mountains, in the northeastern corner of the island. It comprises three municipalities: Artà (7,549 inhabitants), Capdepera (11,929), and Son Servera (12,286). One municipality (Artà) belongs to the North district and two municipalities to the Eastern (Capdepera and Son Servera) [45]. The climate in the area is typically Mediterranean (from the coast to the highest peaks, approximately 600 m) with an annual mean temperature of 16.5°C, a mean rainfall of 805.9 mm, and 70% of mean relative humidity [46]. Plant landscapes are basically limited to those of the Mediterranean biogeographic region with a particular relevance of coastal communities [47]. The three municipalities currently share their main reliance on tourism, having left aside the primary sector of agriculture and livestock, which used to be the main activities throughout their history. Currently the percentage of active people engaged in this economic sector (data from 2010) [45, 48] is only 1.24 for the whole island, and a relevant part of peasants are retired people who continue to cultivate some extension of land not far from the place where they live.

2.2. Informants and Periods of Field Work

The information was obtained from people either born and (almost) permanently located in each concerned territory or having lived there most of their life. The informants’ selection has been basically done on a snowball basis, mostly starting with people known by the authors or by some authors’ friends or relatives. All the authors of the present paper have been born in and live in or have links and frequent contacts with one of the studied territories, which facilitated the approach to the informants. A special emphasis has been made in contacting older people, since we supposed them to possess a higher amount of traditional knowledge due to the years of experience and the possibility of remembering pretouristic times, although young people have also been taken into account. In AE 101 interviews with a total of 179 informants (71% women, 29% men, maximum, minimum, and mean ages 95, 23, and 71 years, resp.) were carried out from 1995 to 2008. In AT 42 interviews concerning 60 informants (63% women, 37% men, maximum, minimum, and mean ages 87, 45, and 71 years, resp.) were performed in 2004 and 2005. In FO, 12 interviews were performed with 14 informants (78.6% women, 21.4% men, maximum, minimum, and mean ages 90, 68, and 80 years, resp.) in 2010 and 2011. In MA 42 informants (40% women, 60% men, maximum, minimum, and mean ages 99, 28, and 77 years, resp.) were interviewed between 2005 and 2011.

2.3. Ethnobotanical Interviews

The conversations were recorded, and pictures were taken during their development, all this with the permission of the informants. We did not use a closed questionnaire and avoided as much as possible asking direct questions, so as not to coerce the interviewees and so diminish their spontaneity. We used a combination of what the ethnographers call nonstructured or nondirected interview and the model termed as structured, direct, or focused interview [49], the latter called semistructured in most ethnobiological literature [50]. In some cases we also practised what the above-cited authors termed group interview, but those with only one informant constituted the majority. Since, as already stated, the authors live in or go frequently to the study areas, participant observation [50, 51] has also been conducted in a large number of cases. Most times more than one conversation with an informant was performed. During the interviews we asked the informants, in addition to their providing data on plant knowledge, to tell us how, when, and where they collected the plants, how they kept them, and how they prepared them for use. One of the principal points in our interviews being medicinal plants, an effort has been made to steer the conversation not only towards comments relevant to human medicine but also touching the health and treatment of domestic animals. So, we asked the informants about plants traditionally used in the area for treating animal illnesses.

2.4. Plant Collection and Identification

Plant materials of all taxa mentioned were collected according to the advice and recommendations of the informants and, whenever possible, together with them. They were identified using the Flora dels Països Catalans [52], the Flora Manual dels Països Catalans [53], and counting, in some cases, on the help of specialists in floristic and systematic botany. For foreign or cultivated species determination we followed [54, 55]. Vouchers are deposited in the herbarium BCN (Centre de Documentació de Biodiversitat Vegetal, Universitat de Barcelona).

2.5. Data Analysis

Data collected were introduced and analysed using a database we had designed [56] to ensure an organized pool of the gathered information from interviews. This permitted the standardisation of data entry and further analysis. This database has been designed as an open source interface, a constantly growing platform for ethnobotanical data collected within Catalan-speaking territories. Technical characteristics of the database are a MySQL server, read on php format and data exported as csv. With comparison intentions, we made an analysis of the coincidences and the degree of novelty between our own data and data from bibliography on ethnoveterinary plant uses in different areas (see the literature quoted in the introduction, especially [27], which constitutes a checklist of world ethnoveterinary plants).

Several quantitative ethnobotany indices accounting for the relevance and/or reliability of folk plant knowledge have been calculated for the ethnoveterinary plant uses in the territories studied: ethnoveterinaricity index (EvI), an adaptation of Portère’s ethnobotanicity index (EI, [57]) to veterinary plant uses; informant consensus factor (FIC, [58]); cultural importance index for each species and for all the territories (CI, [59]), on the basis of all informants, having or not provided veterinarian information. Also, the Jaccard’s similarity index [60] has been calculated from the matrix of all use reports (for the four areas) using R software [61], and its visualisation has been designed as a PCA (principal component analysis) plot. This plot is complementary to a 4-term Venn diagram [62] that compares the number of plant species shared (one-to-one and by groups) among studied territories. Statistical analyses were carried out using XLSTAT 2009 v.3.02 (Addinsoft Corporation) available for Microsoft Excel 2003. Descriptive statistics (including rank, mean, and standard deviation, among other parameters) have been calculated for all the studied variables. One-way ANOVA has been conducted in order to test the differences, if any, in the CI among three studied areas (MA and FO are grouped to avoid a sampling bias). Least significant difference (LSD) test was carried out after ANOVA analysis to identify which pairs are significantly different. Chi-square (χ2) tests are used to compare the parameters (part of plant, pharmaceutical form, etc.) among studied areas.

3. Results and Discussion

In the Catalan and Balearic areas studied, 97 plant species (101 taxa to the levels of subspecies and variety; 49 in AE, 49 in AT, 11 in FO, 17 in MA) have been claimed to be useful for veterinary purposes. Table 1 presents the plants recorded, grouped in alphabetical order of genera, with indication of scientific and local Catalan names, herbarium voucher number, botanical family, part used, pharmaceutical form, administration way, and veterinary and human uses. Table 2 summarizes numerical information on the informants and the territories studied, the plants used, reports, local names, families and related data, and some quantitative ethnobotany indexes calculated for these plant uses in the areas prospected.


Scientific names
(family, voucher specimen)
Catalan namesPart usedPharmaceutical formAdministration wayVeterinary useVRHRArea (CI, CIg)

Achillea ptarmica L* subsp. pyrenaica (Sibth. ex Godr. in Gren. et Godr.) Heimerl (Asteraceae, BCN 24701)camamilla, camamilla de muntanya, camamilla de RojàInflorescenceTisane (with Sambucus nigra)InternalAntidiarrhoeal10AT (0.05, 0.01)
Tisane (with sodium bicarbonate and olive oil)InternalLaxative10AT
Tisane (with Thymus vulgaris and Tilia platyphyllos)InternalSalutiferous11AT

Aeonium* arboreum (L.) Webb and Berthel. (Crassulaceae, BCN 81566)consolvaStemDirect ingestionInternalEgg calcifier30FO (0.21, 0.01)

Agave americana L.
(Agavaceae+, BCN 46860)
figuerassa grossa, figuerassa de margeLeafDirect applicationExternalVulnerary10AE
(0.006, 0.003)

Agrimonia eupatoria L.+
(Rosaceae, BCN 29619)
gremònica, tapaculsLeafTisaneInternalAntidiarrhoeal11AE
(0.006, 0.003)

Allium cepa L. (Liliaceae, BCN 28655)cebaBulbTisaneInternalLaxative12AE
(0.006, 0.003)
Direct ingestionInternalAnticatarrhal (fowl pip)12MA
(0.024, 0.007)

Allium sativum L. (Liliaceae, BCN 24708)allBulbDirect applicationExternalFor stings22MA
(0.071, 0.02)
Direct ingestionInternalSalutiferous11MA
Liniment (with Senecio vulgaris)ExternalAnti-inflammatory (antigotose)11AT (0.017, 0.02)
Liniment (with Bryonia cretica or Umbilicus rupestris)ExternalTo heal wounds22AT

Aloe vera (L.) Burm.f.*
(Liliaceae, BCN 27242)
aloe veraLeafDirect applicationExternalBone reinforcer10MA
(0.024, 0.003)

Althaea officinalis L.
(Malvaceae, BCN 24709)
malvíRootLiniment (with Bryonia cretica or Umbilicus rupestris)ExternalTo heal wounds11AT
(0.017, 0.003

Alyssum maritimum (L.) Lam.* (Brassicaceae, BCN 29622)herba fetgeraFlowered aerial partDirect ingestionInternalAntiicteric10AE
(0.006, 0.003)

Arum italicum Mill.+
(Araceae, BCN 32358)
xèrriaFruitOintmentExternalAnti-inflammatory11AE
(0.006, 0.003)

Arundo donax L.+ (Poaceae, BCN 24720)canyaRootTisaneInternalUnknown10AT
(0.017, 0.003)

Avena sativa L. (Poaceae, BCN 29839)civadaAerial partDirect ingestionInternalBlood pressure regulator10AE
(0.006, 0.003)

Beta vulgaris L.+ subsp. vulgaris (Chenopodiaceae, BCN 24724)bledaLeafMedicinal brothInternalPostpartum coadjuvant (emollient)20AT
(0.033, 0.007)

Brassica oleracea L.+ subsp. oleracea (Brassicaceae, BCN 32181)bròquilFlowered aerial partTisaneInternalAntidiarrhoeal10AE
(0.006, 0.003)

Bryonia cretica L.+ subsp. dioica (Jacq.) Tutin (Cucurbitaceae, BCN 24730)carbassí, carbassinaRootBathExternalAntiparasitic10AT (0.07, 0.01)
Liniment (with Umbilicus rupestris)ExternalTo heal wounds21AT
PoulticeExternalAntidermatose10AT

Calendula officinalis L.
(Asteraceae, BCN 24732)
calèndulaFlower headEssenceExternalAntitoxic11AT
(0.017, 0.003)

Capsella + bursa-pastoris (L.) Medic. (Brassicaceae, BCN 24736)bossa de pastor, caps blancsFlowered aerial partTisaneInternalPostpartum coadjuvant (antihemorrhagic and antihypertensive)11AT
(0.017, 0.003)

Capsicum annuum L.
(Solanaceae, BCN 24737)
pebre coentFruitMaceration in oilExternalInsect repellent20MA
(0.05, 0.007)

Centaurium* erythraea Rafn subsp. erythraea (Gentianaceae+, BCN 29849)herba de santa AuraFlowered aerial partTisaneInternalHypertensive10AE
(0.006, 0.003)

Ceratonia siliqua L.+
(Fabaceae, BCN 32177)
garrofa (fruit)GrainDirect ingestionInternalAntidiarrhoeal10AE
(0.006, 0.003)

Citrus limon (L.) Burm. f.+
(Rutaceae, BCN 46853)
llimoner, llimonera, llimona (fruit)Fruit juiceDirect applicationExternalOcular antiseptic10AE (0.006, 0.01)
Direct ingestionInternalInternal antiseptic11MA
(0.024, 0.01)
Fruit (epicarp)Medicinal soup (boiled rice with lemon peel)InternalAntidiarrhoeal10AT (0.017, 0.01)

Clematis flammula L.*
(Ranunculaceae, BCN 29856)
santjoanet, vidaubaNo dataPoulticeExternalFor swine erysipelas10MA
(0.024, 0.003)

Cucurbita maxima Duch. in Lam. (Cucurbitaceae, BCN-S 1499)rabequet (fruit)FruitOintmentExternalAnti-inflammatory11AE
(0.006, 0.003)

Cucurbita pepo L.+
(Cucurbitaceae, BCN 24757)
carbassaFruitOintmentExternalAntiseptic11AT
(0.017, 0.003)

Daphne gnidium L.
(Thymelaeaceae+, BCN 29687)
tintorell, matapollStemDirect applicationExternalVulnerary10AE (0.01, 0.01)
Antidiarrhoeal10AE, FO
(0.07, 0.01)

Diplotaxis* erucoides (L.) DC. (Brassicaceae, BCN 29861)cap blancFlowered aerial partDirect ingestionInternalGalactofugue10AE (0.006, 0.003)

Dracunculus* vulgaris Schott.
(Araceae, BCN 24765)
herba escurçoneraBulbEmbrocationExternalAntitoxic22AT (0.05, 0.01)
FlowerDirect applicationExternalAntitoxic11AT

Eriobotrya* japonica (Thunb.) Lindl. (Rosaceae, BCN 66823)nisprero, nispro (fruit)LeafDecoctionInternalAntidiarrhoeal24MA (0.05, 0.007)

Eryngium campestre L.
(Apiaceae, BCN 31274)
espinacalFlowered aerial partOintmentExternalAntiophidian10AE (0.006, 0.03)
RootLinimentExternalAntiophidian22AT (0.12, 0.03)
Aerial partDirect applicationExternalAntiophidian44AT
Antialgic10AT

Eryngium bourgatii L.*
(Apiaceae, BCN 24881)
espinacalRootLinimentExternalAntiophidian11AT (0.08, 0.02)
Aerial partDirect applicationExternalAntiophidian44AT

Eucalyptus globulus Labill.+
(Myrtaceae, BCN 29696)
eucalipto, caliptoLeafVapourInternalAnticatarrhal247AE
(0.006, 0.007),
FO
(0.07, 0.007)

Foeniculum vulgare Mill.
(Apiaceae, BCN 24888)
fonollAerial partDirect ingestionInternalAntidiarrhoeal10MA (0.02, 0.003)

Fraxinus excelsior L.
(Oleaceae, BCN 24890)
freixeCortical parenchymaLiniment (decoction with Bryonia cretica)ExternalTo heal wounds11AT (0.03, 0.007)
Bath (decoction with Quercus pubescens)ExternalTo heal wounds11AT

Gentiana acaulis L.+
(Gentianaceae+, BCN 24892)
gencianaNo dataNo dataExternalAntidermatose10AT (0.02, 0.003)

Gentiana lutea L.*
(Gentianaceae+, BCN 24893)
gencianaRootBathExternalVulnerary10AT (0.02, 0.003)

Geranium rotundifolium L.
(Geraniaceae, BCN 29701)
cicutaAerial partOintmentExternalVulnerary11AE
(0.006, 0.003)

Globularia alypum L.
(Globulariaceae*, BCN 53082)
cossiadaTender aerial partDirect ingestionInternalAnorexigen10MA
(0.02, 0.003)

Herniaria hirsuta L.* subsp. cinerea (DC.) Arcang. (Caryophyllaceae, BCN 23330)trencapedraAerial partTisaneInternalDiuretic25MA
(0.05, 0.003)

Herniaria glabra L.+
(Caryophyllaceae, BCN 24901)
herba de mil granes, herba de les mil granesAerial partTisaneInternalAntiicteric10AT (0.02, 0.003)

Hypericum perforatum L.
(Clusiaceae, BCN 29874)
herba de Sant JoanFlowered aerial partOintmentExternalFor mastitis10AE
(0.006, 0.003)

Juniperus communis L. subsp. alpina (Suter) Čelak*
(Cupressaceae, BCN 24910)
ginebre, ginebró, oli de ginebreFruitOintmentExternalAntidermatose32AT (0.05, 0.01)

Juniperus communis L. subsp. communis (Cupressaceae, BCN 29878)ginebreFruitOintmentExternalAnti-inflammatory/ Antialgic/ Antiecchymotic10AE (0.01, 0.007)
Vulnerary10AE

Juniperus oxycedrus L.+
(Cupressaceae, BCN 29879)
càdec, ginebróFruitOintmentExternalVulnerary10AE (0.03, 0.02)
Demulcent10AE
Antifungal10AE
Internal antiseptic10AE
For a sprained leg10AE

Lavandula latifolia Medic.+
(Lamiaceae, BCN 29882)
espígolFlowered stemDirect applicationExternalAntiophidian10AE
(0.006, 0.003)

Lilium* pyrenaicum Gouan
(Liliaceae, BCN 24918)
consolta, consolta grogaBulbLinimentExternalTo heal wounds11AT (0.03, 0.007)
PoulticeExternalTo heal wounds11AT

Linum usitatissimum L.
(Linaceae, BCN 47281)
lli, llinet, oli de llinosa (product)GrainOintmentExternalVulnerary10AE (0.01, 0.007)
EnemaInternalLaxative16AE

Lithospermum* officinale L. (Boraginaceae, BCN 24922)herba pedrera, mill del sol, tabacAerial part with fruitsTisaneInternalPostpartum coadjuvant10AT
(0.006, 0.003)

Lythrum salicaria L.+
(Lythraceae, BCN 29724)
tapaculsFlowered aerial partTisaneInternalAntidiarrhoeal33AE (0.02, 0.01)

Malva sylvestris L.
(Malvaceae, BCN 24924)
malvaNo dataTisaneInternalAnti-inflammatory14FO (0.07, 0.003)
FlowerDecoctionInternalAntiseptic21AT (0.13, 0.03)
Flowered aerial partTisane (with Parietaria officinalis)InternalPostpartum coadjuvant21AT
Tisane (with Parietaria officinalis, Plantago lanceolata, and Plantago major)InternalPostpartum coadjuvant10AT
Diuretic10AT
Tisane (with Umbilicus rupestris)InternalPurgative10AT
Enema (with Parietaria officinalis)InternalPurgative10AT

Marrubium vulgare L.
(Lamiaceae, BCN 29726)
herba del mal roigAerial partTisaneInternalFor swine erysipelas10AE
(0.006, 0.003)

Matricaria recutita L.+
(Asteraceae, BCN 29890)
camamillaInflorescenceDirect ingestionInternalDigestive128AE (0.01, 0.007)
Gastric and intestinal anti-inflammatory113AE

Mentha spicata L.*
(Lamiaceae, BCN 29995)
menta del consolTender aerial partTisaneInternalPostpartum coadjuvant10AE
(0.006, 0.003)

Mentha suaveolens Ehrh.+
(Lamiaceae, BCN 29994)
herbasanaAerial partTisaneInternalAntihelminthic11MA
(0.02, 0.003)

Mercurialis annua L.
(Euphorbiaceae, BCN 29896)
murcarolAerial partTisaneInternalLaxative22AE (0.02, 0.01)
Direct ingestionInternalLaxative10AE

Meum + athamanticum Jacq. subsp. athamanticum (Apiaceae, BCN 24933)herba del meu, meuRootTisane (decoction with Senecio leucophyllus)InternalPostpartum coadjuvant (antiseptic)131AT (0.23, 0.05)
Whole plantTisane (decoction with Saxifraga longifolia)InternalPostpartum coadjuvant10AT

Nicotiana rustica L.+
(Solanaceae, BCN 46839)
tabac potaLeafDirect ingestionInternalEmetic11FO (0.14, 0.007)

Ocimum basilicum L.+
(Lamiaceae, BCN 29897)
fàbregaAerial partTisane (bath)ExternalPuerperal antiseptic10AE (0.01, 0.007)
External antiseptic10AE

Olea europaea L. var. europaea
(Oleaceae, BCN 29898)
olivera, oli d’oliva (product)FruitOintmentExternalFor mastitis10AE (0.06, 0.04)
Antiscabby10AE
Vulnerary10AE
Cicatrizing40AE, FO
(0.07, 0.04)
Antiseptic10AE
Direct applicationExternalHaemostatic10AT (0.03, 0.04)
TabletsInternalSalutiferous11AE
PoulticeExternalInsect repellent30AT, MA
(0.05, 0.04)

Origanum + vulgare* L.
(Lamiaceae, BCN 29742)
orengaFlowered stemDirect ingestionInternalPostpartum coadjuvant10AE
(0.006, 0.007)
Aerial partTisaneInternalInternal antiseptic12FO
(0.071, 0.007)

Oryza sativa L. (Poaceae, BCN 39208)arròsGrainTisane (boiled rice with lemon peel)InternalAntidiarrhoeal12AT (0.02, 0.003)

Parietaria officinalis L. subsp. judaica (L.) Béguinot (Urticaceae, BCN 29745)blet de paret, cama-rojaAerial partBoiled plant and its decoctionInternalLaxative11AE
(0.006, 0.003)

Parietaria officinalis L.
(Urticaceae, BCN 24942)
blet, blet de paretAerial partDecoction (with Malva sylvestris)InternalAntiseptic22AT (0.3, 0.05)
Medicinal broth (with Beta vulgaris, bread and olive oil)InternalPostpartum coadjuvant (emollient)91AT
Tisane (decoction with Malva sylvestris)InternalPostpartum coadjuvant10AT
Diuretic10AT
Purgative11AT
EnemaInternalPurgative11AT

Petroselinum crispum (Mill.) Hill+ (Apiaceae, BCN 29905)julivertLeafDirect ingestionInternalAphrodisiac10AE (0.01, 0.01)
Whole plantDirect applicationInternalAphrodisiac10AT (0.02, 0.01)
RootPoulticeExternalAntiparotid (for mumps)10AE

Pimpinella anisum L.
(Apiaceae, BCN 47278)
anís (fruit)FruitElixirInternalRuminant antistatic10AE
(0.006, 0.003)

Pinus halepensis Mill.+
(Pinaceae, BCN 29826)
pi, pi bordBarkDirect applicationExternalEpithesis10AE
(0.006, 0.007)
ResinOintmentExternalExternal antiseptic13MA
(0.02, 0.007)

Pinus sp. (Pinaceae)pega negra (product)ResinOintmentExternalPuerperal antiseptic10AE (0.01, 0.007)
PatchExternalFor a sprained leg10AE

Pinus sylvestris L.+
(Pinaceae, BCN 27259)
pi, pi roig, pega negra (product)ResinPoulticeExternalEpithesis10AT (0.02, 0.003)

Plantago lanceolata L.
(Plantaginaceae, BCN 24949)
plantatge, plantatge estret, plantatge llargLeafTisane (with Parietaria officinalis)InternalPostpartum coadjuvant (diuretic)10AT (0.02, 0.003)

Plantago major L.
(Plantaginaceae, BCN 24950)
plantatge, plantatge ample, plantatge rodóLeafTisane (with Parietaria officinalis)InternalPostpartum coadjuvant (diuretic)10AT (0.02, 0.003)

Pteridium aquilinum (L.) Kuhn (Polypodiaceae, BCN 46068)falgueraFrondDirect applicationExternalFor flea infestation11AE
(0.006, 0.003)

Quercus ilex L. subsp. ilex +
(Fagaceae, BCN 29932)
alzina, aulinaBarkTisane (bath)ExternalVulnerary62AE (0.05, 0.04)
TisaneInternalAntidiarrhoeal30AE
BathExternalAntiseptic31AT (0.05, 0.04)

Quercus petraea (Matt.) Liebl.* (Fagaceae, BCN 24964)roureInternal barkBath (with Fraxinus excelsior)ExternalAntiseptic30AT (0.07, 0.01)
BathExternalCicatrizing11AT

Ramonda* myconi (L.) Reichenb. (Gesneriaceae, BCN 24965)orella d’ósAerial partTisaneInternalPostpartum coadjuvant (antiseptic)10AT (0.02, 0.003)

Ranunculus parnassifolius L.* (Ranunculaceae, BCN 24967)herba del mal graWhole plantLinimentExternalAntigangrenous11AT (0.2, 0.05)
Liniment, bathExternalAntiseptic45AT
Liniment, bathExternalResolutive45AT
Liniment, poulticeExternalAntineoplastic56AT

Rosmarinus officinalis L.
(Lamiaceae, BCN 29937)
romaníFlowered stemTisaneInternalPostpartum coadjuvant10AE
(0.006, 0.007)
Aerial partDirect ingestionInternalAntidiarrhoeal10FO (0.07, 0.007)

Ruta chalepensis L.
(Rutaceae, BCN 29940)
rudaAerial partDirect ingestionInternalCarminative10AE (0.006, 0.04)
Ruminant antistatic20MA (0.07, 0.04)
Direct applicationExternalPostpartum coadjuvant (antiseptic)30AT (0.10, 0.04)
Tranquilizer10FO (0.14, 0.04)
Flea repellent10FO
Embrocation (with Bryonia cretica or Umbilicus rupestris)ExternalTo heal wounds12AT
LinimentExternalTo heal wounds12AT
Anti-inflammatory10AT
No dataInternalAntihelminthic110MA

Sambucus nigra L.
(Caprifoliaceae, BCN 29943)
sabuquer, sabuc, flor de sabucInflorescenceFumigationExternalFor mastitis10AE (0.006, 0.03)
FlowerTisane (with Achillea ptarmica)InternalAntidiarrhoeal21AT (0.15, 0.03)
TisaneInternalIntestinal antiseptic214AT
Essence (with Achillea ptarmica)InternalAntidiarrhoeal21AT
EssenceInternalIntestinal antiseptic214AT
FruitSyrupInternalIntestinal antiseptic 19AT

Santolina chamaecyparissus L.* (Asteraceae, BCN 29944)camamillaFlower headTisaneInternalInternal antiseptic15FO (0.07, 0.01)
BathExternalOcular antiseptic28MA (0.07, 0.01)
EnemaInternalPuerperal antiseptic10MA

Saxifraga longifolia Lap.* (Saxifragaceae)corona de reiAerial partTisane (with Ramonda myconi or Meum athamanticum)InternalPostpartum coadjuvant (antiseptic)10AT (0.02, 0.003)

Saxifraga paniculata Mill.+ (Saxifragaceae, BCN 24992)corona de reiAerial partTisaneInternalIntestinal anti-inflammatory11AT (0.03, 0.007)
Postpartum coadjuvant10AT

Scabiosa columbaria L.*
(Dipsacaceae, BCN 24993)
escabiosa, escapiosa, herba d’escapiosaAerial partTisaneInternalAntiparasitic10AT (0.02, 0.003)

Sedum + sediforme (Jacq.) Pau* (Crassulaceae, BCN 29792)mort-i-viu, herba de Sant PereLeafPoulticeExternalAnti-inflammatory/
Antialgic/
Antiecchymotic
10AE (0.01, 0.007)
Antiseptic10AE

Sedum + telephium L.*
(Crassulaceae, BCN 24995)
arròs de paret, bàlsam, herba grassa, matafocsLeafOintmentExternalAntidermatose22AT (0.03, 0.007)

Sempervivum montanum L.* (Crassulaceae, BCN 24996)matafoc de muntanyaAerial partLinimentExternalAntidermatose10AT (0.02, 0.003)

Senecio leucophyllus L.*
(Asteraceae, BCN 24998)
herba blancaAerial partTisane (decoction with Meum athamanticum)InternalPostpartum coadjuvant10AT (0.02, 0.003)

Solidago virgaurea L.*
(Asteraceae, BCN 25007)
vara d’orFlowered aerial partTisaneInternalAntitoxic10AT (0.02, 0.003)

Sonchus oleraceus L.
(Asteraceae, BCN 29953)
llipsó, lletissóAerial partDirect ingestionInternalGalactogenous10AE (0.006, 0.01)
Liniment (with Senecio vulgaris)ExternalAnti-inflammatory11AT (0.05, 0.01)
Antigotose11AT
LinimentExternalVulnerary11AT

Sorbus aucuparia L.*
(Rosaceae, BCN 25009)
moixera de guillaAerial partDirect applicationExternalAntiviral10AT (0.02, 0.003)

Tanacetum parthenium (L.) Schultz Bip.+ (Asteraceae, BCN 29960)tanarida, herba del remuc, camamilla, camamilla amargant, camamilla borda, camamilla de parets, danarida, herba danaridaFlowered aerial partTisaneInternalRuminant antistatic30AE (0.08, 0.08)
Direct ingestionInternalRuminant antistatic70AE
TisaneInternalAntiicteric10AE
InternalAntidiarrhoeal20AT (0.15, 0.08)
InternalDigestive23AT
InternalAntinausea11AT
InternalUnknown50AT
TabletsInternalRuminant antistatic20AE
InternalAntiicteric10AE

Taraxacum* officinale Weber in Wiggers (Asteraceae, BCN 25948)dent de lleóLeafDirect ingestionInternalBone reinforcer11AE
(0.006, 0.003)

Thymus vulgaris L.
(Lamiaceae, BCN 29961)
farigola, frígula, frigolaFlowered stemTisane (bath)ExternalAntiseptic540AE (0.06, 0.03)
Ocular antiseptic210AE
Vulnerary18AE
Direct ingestionInternalCarminative11AE
Tender aerial partTisaneInternalPostpartum coadjuvant10AE

Thymus serpyllum L. subsp. chamaedrys (Fries) Čelak+ (Lamiaceae, BCN 25019)farigoleta, farigoleta de muntanya, serpóFlowered aerial partTisaneInternalAntidiarrhoeal11AT (0.02, 0.003)

Thymus serpyllum L. subsp. nervosus (Gay ex Willk.) Nyman*
(Lamiaceae, BCN 25020)
farigoleta, farigola de muntanya, farigola de pastor, farigolet, xerpollFlowered aerial partTisaneInternalAntidiarrhoeal31AT (0.05, 0.01)

Triticum aestivum L.
(Poaceae, BCN 29963)
blatBranPoulticeExternalDiuretic10AE
(0.006, 0.003)

Umbilicus rupestris (Salisb.) Dandy+ (Crassulaceae, BCN 25029)barret de paretAerial partLiniment (boiled with olive oil and Allium sativum, Althaea officinalis, Bryonia cretica, Lilium pyrenaicum, Ruta chalepensis, Petroselinum crispum, Sedum sp.)ExternalTo heal wounds11AT (0.05, 0.01)
Direct applicationExternalTo heal wounds11AT
TisaneInternalPurgative10AT

Urginea maritima (L.) Baker
(Liliaceae, BCN 58049)
ceba marinaBulbMaceration in oilExternalInsect repellent20MA
(0.05, 0.007)

Urtica dioica L. (Urticaceae, BCN 29814)ortiguesAerial partDirect applicationExternalAphrodisiac10AE
(0.006, 0.003)

Veratrum album L.
(Liliaceae, BCN 25034)
veladreAerial partTisaneExternalAntiparasitic (for mange in sheep)10AT (0.05, 0.01)

Verbascum sinuatum L. (Scrophulariaceae, BCN 29967)trepóFlowerTisaneInternalAntidiarrhoeal11AE
(0.006, 0.003)

Vicia faba L. (Fabaceae, BCN 46826)faveraGrainDirect ingestionInternalFor studs’ fertility enhancement10AE
(0.006, 0.003)

Vitis vinifera L. (Vitaceae, BCN 29972)vinya, vi (product), vinagre (product)Fruit juiceVinegarExternalAnticatarrhal11AE (0.02, 0.02)
Diuretic10AE
Antiseptic11AE
Tranquilizer10FO (0.14, 0.02)
Medicinal wineInternalRestorative10MA (0.02, 0.02)
Blue comb10FO


AEATFOMATotal

General Data
 Extension (km2)135829481.22381971.2
 Population1187184526914731764164155
 Number of total informants179601442295
 Number of informants with veterinary reports4641413104
 Number of taxa in the flora of the territory1650(1)1600(2)574(3)780(4)
 Total of livestock (includes cattle, sheep, goats, pigs, horses, and poultry)2345153(5)28088(6)3229911(7)5525414
Ethnoveterinary and other ethnobotanical data
 Number of taxa with veterinary uses49491117100
 Number of species with veterinary uses4847111796
 Number of veterinary use reports1061461628306
 Number of coincidental human and animal medicine use reports33104416157
 Number of local Catalan names of plants with veterinary uses55701118154
 Number of botanical families containing plants with veterinary uses3127101341
 Number of veterinary reports/number of informants with veterinary reports2.303.564.002.152.94
 Number of animal feed taxa73211416
 Number of human medicinal taxa33422092117
 Percentage of veterinary uses coincidental with human medicinal ones30.152.238.55042.9
Ethnobotanical indexes
 Ethnoveterinaricity index (EvI)0.030.030.020.02
 Informant consensus factor (FIC)0.540.680.330.400.67
 Average index of cultural importance (CI) calculated per area0.010.050.100.040.04
 Average index of cultural importance (CI) calculated for all studied areas0.010.010.020.010.01

(1)[77]; (2)J. Vigo (pers. comm.); (3)[79]; (4)[80]; (5)[81]; (6)[81]; (7)Data for the whole Balearic archipelago [73].

Apart from the plants used against animal diseases, a considerable percentage of plant species are employed in the different areas as fodder: 21% (AT), 73% (AE), 16% (MA), and 14% (FO). This paper being specifically devoted to medicinal uses, we did not consider all feed plants as having an ethnoveterinary application. Anyway they, too, contribute to animal health, and in many cases the informants attribute them with medicinal properties complementary to the nutritional effect. These plants fit within the category of folk functional foods, proposed by Rigat et al. [37] to include plants traditionally used as nutraceuticals or food medicines, terms usually applied in human medicine, but perfectly transposable to veterinary medicine. As Pearson [15] remarked, there is a frequent possible confusion between feed and drug in ethnoveterinary.

The number of veterinary plant taxa (101) is intermediate between those recorded in the two precedent investigations on this subject in the Catalan cultural area (89 in Montseny [31], 195 in Pallars, Pyrenees [36]). It also occupies a medium position in a ranking going from 36 to 280 taxa used for animal health care in European, African, Asian, and American territories [12, 18, 19, 22, 23, 3335]. In fact, it is not far from the average of the data contained in the 10 studies reported in the preceding lines (121.3 average taxa for the 11 studies), representing a large geographical range and up to a third of the 451 taxa collected in a world checklist of veterinary botanicals [27]. The big differences among plant number in these areas may be attributed, apart from geographical and possible cultural facts, to the different extension of the territories prospected (from small communities to entire countries). In any case, we can consider the number of plant taxa reported in the present study as rather high, taking into account the decrease in folk animal health practices experienced in industrialised areas [1].

The ten most reported plants were Tanacetum parthenium (24 use reports), Parietaria officinalis (15), Ranunculus parnassifolius (14), Meum athamanticum (13), Olea europaea (13), Quercus ilex (12), Ruta chalepensis (12), Sambucus nigra (10), Thymus vulgaris (10), and Malva sylvestris (9). Among these plants, there are some of the most reported also in other Mediterranean territories, especially Malva sylvestris, Parietaria officinalis, Ruta chalepensis, Sambucus nigra, and Thymus vulgaris [18, 30, 31, 33, 35, 36]. An originality of this study is the report in top position in the ranking of Meum athamanticum and Ranunculus parnassifolius. These two central European high mountain plants [53], reported, respectively, for the second and first time in veterinary (see Section 3.2 and Table 1), are much appreciated in one of the regions studied (AT), the first one as postlabour coadjuvant and the second one for different kinds of uses, antineoplastic included. Another high mountain Ranunculus species (R. aconitifolius) has been recorded from Occitan shepherds of a French Central Massif region with a use (resolutive) coincidental with one of those of R. parnassifolius in the studied area [26]. It is worth mentioning also the plant occupying the 11th position in our list as per number of reports, Eryngium campestre. This plant, only reported in veterinary to date with the same use in another Catalan region [31], and with different uses in Andalusia [34] and Aragon [63], is widely employed in two of the areas prospected (AE, AT) as an antiophidian. In addition, another species of the same genus (E. bourgatii, not reported to date in veterinary) occupies the 13th position in the list also with the same use. These two taxa were not recorded (as another congeneric one, E. foetidum, was) in a comprehensive checklist of plants used against snake bite, containing 773 taxa [64], and only one reference to an undetermined Eryngium sp. is provided in a work on Turkish ethnoveterinary [65].

The families containing more taxa with claimed veterinary uses are Lamiaceae (10 taxa), Asteraceae (9), Apiaceae (6), Liliaceae (6), Pinaceae (6), and Crassulaceae (5). Some of them (Apiaceae, Asteraceae, Lamiaceae, Liliaceae) are at the same time large families and typically abundant in Mediterranean areas, and they are among the more represented families in most ethnobotanical works in this biogeographical region ([66] and references therein). Another one, Pinaceae, not so big in terms of number of taxa, is landscape dominating in significant parts of the studied areas. All these families but one (Crassulaceae) are among the top ten in the recent world inventory of veterinary ethnobotany [27]. Most of these families are coincidental with the main ones appearing in other studies in the Catalan linguistic area [31, 36], as well as in other Iberian [3335] and other Mediterranean [18, 30] territories. In an area within Argentina, a great distance from those here studied, the cosmopolitan families Asteraceae and Lamiaceae are coincidental as some of the most reported ones, but others, such as Verbenaceae and Zygophyllaceae, make a difference [23]. Similarly, in a South African region Asteraceae also occupy a preeminent place, but not Lamiaceae, whereas Capparaceae and Euphorbiaceae are particularly relevant [19], contrarily to the currently considered area. More differential families may be recognized in a study performed in an Indian territory, where even the Asteraceae do not appear and the Lamiaceae are only represented by one report among results given for 17 families [17]. This predominance as more reported families of those large and with many representatives in the flora of the area considered agrees with the statement of Johns et al. [67] that the closer to the user a plant grows, the more it is employed. We could also verify this point in many works on folk plant uses in human medicine ([68] and references therein). Of course, the presence of well-known medicinal plants in all these particularly relevant families goes in the same sense. The Crassulaceae, located in position 23 in this catalogue and with only 39 taxa present in Catalan language territories (an area much larger than the one we cover) [54], constitute a particularity of the studied zone. One cultivated/subspontaneous and four wild taxa of four genera belonging to this family are profusely used (11 reports), mostly externally, for wounds and dermatologic affections, although the internal use of Aeonium arboreum on the island of Formentera (three reports) as a hens’ egg calcifier (i.e., to add calcium and so to reinforce the eggshell) should be highlighted.

3.1. Comparison among the Studied Territories

In this section, graphical information and descriptive statistics are presented in order to give a detailed interpretation of the comparison among prospected territories. On the one hand, and according to the 4-area Venn diagram of Figure 2, only two species (in the very centre of the graph) have been cited in all the territories; these are Olea europaea var. europaea and Ruta chalepensis. If we look, on the one hand, at the Venn diagram, we notice that the information from Alt Empordà and High River Ter Valley is nearly independent in itself, but Formentera shares almost all the uses and plant species reported (9 shared versus its total of 11). Meanwhile, Mallorca appears in the crossroad in between the three other areas, and nearly half of all the species cited by Mallorcans (9) are different from the species of the other places studied. Notwithstanding, there are 8 plant species cited in Mallorca uniformly distributed among the rest of the areas. No plant species coincidences were found among the groups AE-AT-FO and AT-MA-FO, probably because of the lesser data from Formentera included in the analysis.

On the other hand, if we look at the PCA plot (referring similarities between use reports (Figure 3)), we also find a convergence zone where several use reports from the four areas coincide. The condensation of Mallorcan data at this point could be explained due to the eight largely distributed species above mentioned, as well as the data from Formentera, which appear close to this area for sharing many of its taxa with the other regions. Moreover, the AE data spread distribution of the PCA plot, as opposed to AT, may be explained because many use reports are cited by a unique informant, so that the similarity line is upward deflected. In short, PCA plot reveals that, considering not only plant species but UR, islands have ethnobotanical similarities and there are shared UR citations with the four regions considered in the study.

One-way ANOVA and LSD test show statistically significant differences in the CI among four studied areas ( ) excepting for AT versus MA ( ). When MA and FO are grouped, no significant differences between these two Balearic Islands and AT were found ( ). Chi-square tests also show differences between observed and expected frequencies in all studied areas for the three variables included: part used ( ), pharmaceutical form ( ), and veterinary uses ( ).

The comparison of ethnoveterinary data from the four areas leads us to consider that the common heritage of plant uses (and specifically for veterinary treatments in the present work) throughout the Catalan-speaking territories is nuanced by local features. It has to be emphasized that this is the first cross-regional ethnobotanical comparison made up with Catalan data. Similarly to other comparative studies using coordinated methodology and dealing with ethnobotanical data [18, 68, 69], it is very difficult to assure that there is a standard traditional veterinary knowledge among the four areas without contemplating floristic, bioclimatic and sociohistorical aspects.

3.2. Comparison with Previous Reports and Novelty in Uses in the Regions Studied

A certain number of plant species and plant uses are new or very scarcely previously reported in ethnoveterinary. We have first compared our results with a recent world catalogue of plants used in this field [27], built with information from 222 publications and including data on 451 taxa at specific or subspecific levels, 308 genera and 116 families. From this comparison, we found that 42 species and one subspecies, 17 genera and five families do not appear in this inventory and must thus be considered new or very scarcely reported as useful in veterinary. In addition, 27 taxa are also not very commonly used in veterinary, since they were reported only once in the world inventory, 17 of them with data coming from a previous work of our team in Montseny [31], an area belonging to the same cultural community of the currently considered zones. These new or rarely recorded taxa have been crossed with a review of plants used in ethnoveterinary in Italy ([30], not quoted in [27]), containing information on 280 species or infraspecific taxa belonging to 71 families. In this review, eight species, six genera, and two families not listed in [27] appeared, as well as six of the species cited only once. Thus, the novelties contributed in the present paper are 34 species and one subspecies, 11 genera, and three families, plus 21 species only mentioned once. Irrespective of the wide reach of the two reviews considered, it is sure that the amount of new taxa could be reduced with a still more comprehensive literature cross (e.g., four plants reported in this study and only previously cited once in veterinary according to the above-mentioned sources have been very recently mentioned in Andalusia [34], and one, Meum athamanticum, not appearing in any of the checklists mentioned was already reported by Font Quer in 1961 [70]). Nonetheless, we believe that in any case the number of taxa of different taxonomic level not, or very rarely, previously reported as used in veterinary is significant. The comparatively small amount of work on ethnoveterinary in Europe could contribute to explain this high level of new information.

3.3. Parts of Plant Used, Preparation and Administration Forms, and Plant Use Categories

A summary of the top ten used plant parts, preparation and administration forms, is graphically represented in Figure 4. This figure also includes the ten most cited veterinary use categories, which are compared to human medical indications in Section 3.5. The plant parts most commonly used for veterinary remedies preparation, concerning the general overview of the four areas, are aerial parts (leaves and stems; 71 reports), flowered aerial parts (44 reports), fruits (26 reports), roots (25 reports), and leaves (19 reports). However, it is outstanding that only aerial parts and leaves are represented in the four areas, meaning that leaves (alone, or together with the stems in which they are inserted) are the most popular organ in terms of geographical extension. These numbers do not differ much from other ethnoveterinary studies [31, 3335] neither do they from human ethnopharmacological works for the same areas [66, 71, 72], where aerial parts and leaves are at the top of list of plant part analysis. The percentage of internal administration form (54.03%) is not much higher than the external (45.97%), but still tisanes are the preferred preparation method (with 86 reports) for animal traditional therapies. Tisanes are not difficult to prepare but, after tisane, we count the direct ingestion (34 reports) and direct application (31 reports), which are even easier ways to treat animals (most of them are grass-eating domestic animals). With particular regard to excipients—apart from water—olive oil has to be counted as the most important in the four areas. The use of olive oil ointments for external administration appears in a fourth place in the preparation classification, and it is especially formulated as vulnerary, cicatrizing, and against dermatologic ailments.

The most cited veterinary use category as an absolute value for all the territories altogether is the postpartum coadjuvant. However, this is not a significant set since there are 42 reports out of 46 that have been collected for the AT area. For the whole area prospection, the most representative veterinary indication is the antidiarrhoeal. Indeed, plants aimed to treat gastrointestinal disorders are frequently on the top of the latest ethnoveterinary usage lists [23, 34, 35]. Top veterinary uses concerning every study territory separately are diverse enough: vulnerary for AE, postpartum coadjuvant for AT, egg calcifier for FO, and insect repellent for MA. The reason of these differences may lie on the type of livestock treated; for example, results from Mallorca have a socioeconomic bias on sheep treatment since these animals have historically been the first islander meat resource, well ahead of the pig [73]. The treatment of sheep against fly larvae explains that many plant citations have been made for insect repellent.

3.4. Quantitative Ethnobotany: Indices Assessing the Importance, Persistence, and Reliability of Veterinary Plant Uses in the Regions Studied

The ethnoveterinaricity index (EvI), which we have defined here adapting the classical ethnobotanicity index to include only use reports of plants concerning animal health, is low in all the studied areas. It oscillates between 0.02 and 0.03, this meaning that only around 2-3% of plants present in these territories are claimed to be useful in veterinary. General ethnobotanicity indices or indices referring to all medicinal plant uses in Mediterranean territories oscillate between 0.05 and 0.51, the average value for 21 territories being 0.22 [66]. The percentage of plants used in veterinary is, logically and in all cases, lower than general ethnobotanicity indices. In the present case, it is also lower than in the two previous reports on Catalan ethnoveterinary (0.06 in Montseny [31] and 0.13 in Pallars [36]), but similar to that recorded in another Iberian area (0.02 in Navarra [33]).

The mean informant consensus factor (FIC) considering the four areas studied is 0.67, and it ranges from 0.33 to 0.68, being bigger in the two Catalonian areas (AE 0.54, AT 0.68) than in the Balearic ones (FO 0.33, MA 0.40). This index, with the maximum value of 1, shows the consistency of uses among the informants of a given territory, and thus it is one of the indicators of reliability for such uses. The values of the Catalonian areas are close to that from Montseny, 0.66 [31]. In general, FIC values for ethnoveterinary are clearly lower than those of works on human medicinal uses in the same territories (AE 0.91, AT 0.87, MA 0.71, FO 0.73) ([66, 71, 74], Mayans, Carrió, and Vallès, unpubl. res.). This suggests a preeminence of human medicine over veterinary, at least in current times, in the society prospected: veterinary uses are less homogeneous and consistent that human medical ones, since they are in fact perceived nowadays as less relevant, less necessary. In any case, it is interesting to remark that the ethnoveterinary are proportional to the general (for all medicinal plant uses) ones in each territory, confirming the above-described fact. Most works on ethnobotany of veterinarian plants do not mention FIC values. The ones reported for eight zones of Navarra (Western Pyrenees, Spain) range from 0 (in the main cities areas) to 0.63, the mean being of 0.37 [33]. These values are slightly lower, but similar to those recorded in the present paper; in Navarra, the FIC for general medical ethnobotany is also higher than the veterinary one (0.65 [75]). Finally, it is worth mentioning that FIC of the whole territory studied (0.67) are lower but not very far from those for human medicinal uses in some Mexican and Indian regions (0.75, 0.79 [7678]). The latter were recorded in countries where folk medicinal plant knowledge is considered relevant and currently in use. To summarize, there is not a very pronounced agreement in ethnoveterinary plant uses, but neither it is extremely low, when taking into account the indicative figures from other territories and the current relevance of domestic animals along with the modern way to address their health troubles.

Another way to assess the relevance of folk plant uses is the recently described cultural importance index (CI, [59]). The global values of this index are low in the areas prospected (Table 1), ranging from 0.01 to 0.02. This is not surprising taking into account that in each territory, and in all of them together, the number of plants claimed as useful is high, and for many of them a scarce number of reports has been collected. In addition, even the interviewees who did not report any veterinary use are counted. The CI ranges per area, also calculated on the basis of all informants, not only those having provided veterinarian information, are slightly or clearly—depending on the cases—higher: 0.06–0.08 (AE), 0.02–0.27 (AT), 0.07–0.21 (FO), and 0.02–0.07 (MA). Just to give an example of the different CI values in a veterinary and in a human medicinal ethnobotanical survey, Santolina chamaecyparissus in MA has 0.07 for ethnoveterinary and 0.81 for human pharmaceutical ethnobotany [74], this indicating the much higher number of informants that report medical uses as opposed to those claiming veterinary ones. This index was rather designed to highlight the most relevant plants used for a specific purpose in a particular cultural area; this is why the most reported plants bear the larger indices. This index assesses the relevance of a plant in a culture. Here culture can be understood either in its broad sense (in our case, the Catalan one, common to all studied areas) or in its restricted sense, distinguishing in the present case high mountain (AT), medium mountain and plain (AE) and insular (FO, MA) cultures. All these cultures in a more restricted sense are shaped on the one hand by belonging to a linguistic community and on the other hand by geographical and socioeconomic conditions: as stated above (Section 3.1); the common base is modelled by and diversified with local specificities. The top ten plants regarding report number, quoted in the first paragraphs Section 3, have, logically, the highest CIs in the whole area studied, but some plants not present in this list bear the highest CIs in particular territories, such as Aeonium arboreum (FO), Allium sativum, and Santolina chamaecyparissus (MA). The description of this index is recent, and so very few papers include it in their analyses. Nevertheless, an ethnoveterinary study of an Iberian area, Arribes del Duero (Salamanca, Western Spain), also shows a high number of low CIs (with a minimum value of 0.04), but at the same time some very high, four of them higher than 1.

3.5. Comparison between Veterinarian and Human Medicinal Plant Uses

Table 1 shows the agreements between veterinary and human medicinal plant uses in the areas studied, meaning the strict coincidence not only of the plant employed but of its claimed properties as well. The number of total human and veterinary medicine uses is presented in Table 2. There are of course many more human medicinal uses different from those addressed to animal health ([66, 71, 74], Mayans, Carrió, and Vallès, unpubl. res.), but we have highlighted here only the uses that are common to both people and animals.

Table 2 shows that the number of plants reported to be useful in veterinary medicine is dramatically low as compared with that of those indicated to be used in human medicine in the same territories (15.3% in AE, 21.8% in AT, 12% in FO, 14.5% in MA). Yet the proportion of informants who reported veterinary uses is low, also in every area prospected (absolute figures in Table 2; 25.7% in AE, 68.3% in AT, 28.6% in FO, 31% in MA). Facing this situation, the question arises as to whether it could be the consequence of a bias in data recording. It is true that when talking about medicinal plants (one of the main focuses in our ethnobotanical interviews), it is implicitly clear for both interviewers and interviewees that human medicinal uses have to be addressed, whereas the reference to veterinary uses is not so evident. So, we must admit a slight weight of this factor in this difference between human and animal medicinal plant use reports. Nevertheless, in many cases in which the point of ethnoveterinary uses is explicitly present in the conversations, this does not significantly increase the information on animal health care. In addition, the number of veterinary plants recorded in the areas prospected is not lower than those published for other studies in the same biogeographical region [18, 31, 3336]. Moreover, 68.3% of AT informants provided ethnoveterinary data as compared with 25.7% in AE, but the increase of information only represented 6.5%. We believe that the decline in human dependence on domestic animals in so-called western societies explains basically the unbalance between both kinds of medicinal plant uses. In this sense, it is interesting to remark that AT (the territory studied with a larger proportion of informants supplying ethnoveterinary information and of veterinary uses recorded) is a high mountain area in which domestic animals still play a significant role, at least more than in the other places.

In any case, the 306 veterinary use reports of 101 taxa in the four areas considered constitute a large therapeutic corpus, with a not insignificant part in agreement with human medicinal uses also claimed by the informants. The proportion of coincidental human and animal plant-use categories in all the studied areas is 42.9%, ranging from 30.1% to 52.2% in the different territories (Table 2). In terms of number of reports of the same use of a plant in human and animal health, the figures are also high (Table 2), representing a 52.7% of agreement when all areas are considered together, and being of 31.1% in AE, 69.8% in AT, 25% in FO, and 59.3% in MA. Again, AT is the territory with the highest coincidence in use categories and reports, this indicating a still important degree of validity of veterinary practices in this area since the more animal health care uses persist, the more they may coincide with those for human health troubles, in general more operative and easily recalled.

In most cases, the plants for which human medicine reports are coincidental with veterinary ones are among the most commonly used to address people’s ailments. As an example, in MA, four of the plants so considered (Allium sativum, Citrus limon, Herniaria hirsuta, and Santolina chamaecyparissus) appear in the list of the top five medicinal species in the area. In these cases plant preparations for animals are often similar to those for humans [74], showing on the one hand how important animals were in times gone by and on the other hand the proximity of veterinary and human medicine and so the relevance of ethnoveterinary data as evidences for phytotherapy in general. In AE the panorama is similar (present data and [66]) to one of the top species (Allium sativum) coincidental with MA.

Two use categories in which there is a convergence of veterinary and human medical uses are gastrointestinal and skin troubles. On the one hand, digestive, antidiarrhoeal, gastrointestinal antialgic and anti-inflammatory are uses corresponding to usually nonsevere chronic illnesses very often treated with folk phytotherapeutic remedies ([34, 66] and references therein). On the other hand, skin affections may also be nonsevere troubles (such as warts) and have a particular incidence in rural societies, in people dealing with agricultural and livestock-raising activities (wounds and some kinds of skin infections), this kind of affection being almost as common in humans as in the animals they take care of. Conversely, a use category that was once shared by people and domestic animals, labour and postlabour coadjuvant, is now almost exclusively restricted to animals, basically cows. The explanation is evident: the medical assistance in labour has increased dramatically more in human beings than in livestock, apart from the fact that many labour coadjuvants may have abortive effects if used in a nonadequate manner or period of time, and there is a higher vigilance of this aspect in people than in domestic animals.

3.6. Concluding Remarks

Our research in four European areas has verified that, as Mathias et al. [3] wrote, ethnoveterinary practices constitute viable alternatives or complements to conventional, Western-style veterinary medicine. The collection of information on ethnobotanical uses of plants in veterinary medicine, as done in the present work, is the first step of the process that can permit the passage from folk, often small-scale, uses to industrial or at least medium-scale applications. It is undoubtedly one of the beneficial and appropriate ethnoveterinary interventions that, in words of Wanzala et al. [1], represent a major challenge in the development of this discipline in the 21st century. Muhammad et al. [16] stated that these data provide a basis for further validation of practices and plant uses in the context of a professional approach to ethnoveterinary medicine. Additionally, we stress that recording these data is already in itself a part of this validation, since it provides scientific evidence of plant uses, after which, chemical, pharmacological, and other issues should be addressed. Some examples of legislation and herbal products development in western Europe [82] make us believe that further ethnobotanical studies in the field of veterinary are needed, followed by a coordination with different stakeholders (livestock raisers, veterinary surgeons, chemists, health policy managers and deciders, pharmaceutical firms, among others) in order to integrate ethnoveterinary knowledge—as we have seen, closely related to human ethnomedicinal one—in health policies.

As for all domains of ethnobiology, the inventory of ethnoveterinary practices is urgent, mostly in industrialised countries. Concerning specifically animal health care, in relatively few years we have passed, at least in southwestern Europe, from a lifestyle in which, according to a popular saying, the illness of the mule was considered worse for a rural family than a trouble in a member of the family to a situation of almost no dependence on domestic animals and from the practical absence of veterinary doctors and industrial medicines to the inverse situation even in the smaller population nuclei. The popular saying regarding the mule, obviously an exaggeration, can still be heard amongst elderly people in the regions prospected, but today the situation is different. Thus, a certain amount of ethnoveterinary knowledge in the areas described is no longer in practice and must be collected—not only as a cultural and biological heritage, but also as possible sources for new drugs for animals and humans—before it is too late.

Acknowledgments

First of all the authors thank all the informants, who wanted to share with them their considerable and often profound knowledge of plant uses and, in general, biodiversity management. Dr. J. M. Campanera, Universitat de Barcelona, is thanked for his support in statistical questions, Professor J. Vigo, Universitat de Barcelona, for floristic information, and S. Pyke, Jardí Botànic de Barcelona, for his revision of the English language. Research was partially supported by projects subsidized by the Municipal Council of Figueres (XI Beca de Recerca “Ciutat de Figueres”, 2009), the Catalan Agency for University and Research Grants Management (AGAUR, projects 2009ACOM00012 and 2009ACOM00013), and the Spanish Ministry for Science and Innovation (MICINN, projects SEJ2007-60873/SOCI and CSO2011-27565). The support of the Centre d’Estudis Comarcals del Ripollès is also thanked. E. Carrió received a predoctoral grant of the Spanish Ministry of Education, Culture and Sport (AP2007-00766). The authors also received funding from GReB (from the abbreviation in Catalan, Biodiversity and Plant Biosystematics Research Group, Catalan government, AGAUR 2009SGR439).

References

  1. W. Wanzala, K. H. Zessin, N. M. Kyule, M. P. O. Baumann, E. Mathias, and A. Hassanali, “Ethnoveterinary medicine: a critical review of its evolution, perception, understanding and the way forward,” Livestock Research for Rural Development, vol. 17, no. 11, 2005. View at: Google Scholar
  2. E. Mathias, C. M. McCorkle, and T. W. Schillhorn Van Veen, “Introduction: ethnoveterinary research and development,” in Ethnoveterinary Research and Development, C. M. McCorkle, E. Mathias, and T. W. Schillhorn Van Veen, Eds., pp. 1–23, Intermediate Technology Publications, London, UK, 1996. View at: Google Scholar
  3. E. R. Mathias, M. Martin, and C. M. McCorkle, Ethnoveterinary Medicine: An Annotated Bibliography of Community Animal Healthcare, ITDG, London, UK, 2001.
  4. V. Van den Eynden, P. Vernemmen, and P. Van Damme, The Ethnobotany of the Topnaar, Ghent University & Commission of the European Comunity, Ghent, Belgium, 1992.
  5. D. E. Moerman, Native American Ethnobotany, Timber Press, Portland, Ore, USA, 1998.
  6. S. Brüschweiler, Plantes et savoirs des Alpes. L’exemple du val d’Anniviers, Éditions Monographic, Sierre, 1999.
  7. M. Rigat, T. Garnatje, and J. Vallès, Plantes i gent. Estudi etnobotànic de l’Alta Vall del Ter, Centre d’Estudis Comarcals del Ripollès, Catalonia, Ripoll, Spain, 2006.
  8. Ch. Ghosh and A. P. Das, “Plants of ethnobotanical significance for the tea garden workers in Teral and Duars of Darjeeling in West Bengal, India,” in Advances in Ethnobotany, A. P. Das and A. K. Pandey, Eds., pp. 133–147, Bishen Singh Mahendra Pal Singh, Dehra Dun, India, 2007. View at: Google Scholar
  9. A. Pieroni, “People and plants in Lëpushë: traditional medicine, local foods and post-communism in a northern Albanian village,” in Ethnobotany in the new Europe. People, health and wild plant resources, M. Pardo-de-Santayana, A. Pieroni, and R. K. Puri, Eds., pp. 16–50, Berghahn Books, Oxford, UK, 2010. View at: Google Scholar
  10. E. Geerlings, Sheep husbandry and Ethnoveterinary knowledge of Raika sheep pastoralists in Rajasthan, India, M.S. thesis, Environmental Scences, Wageningen University, The Netherlands, 2001.
  11. C. Lans, T. Harper, K. Georges, and E. Bridgewater, “Medicinal and ethnoveterinary remedies of hunters in Trinidad,” BMC Complementary and Alternative Medicine, vol. 1, article no. 10, 2001. View at: Publisher Site | Google Scholar
  12. C. Lans, N. Turner, T. Khan, G. Brauer, and W. Boepple, “Ethnoveterinary medicines used for ruminants in British Columbia, Canada,” Journal of Ethnobiology and Ethnomedicine, vol. 3, article no. 11, 2007. View at: Publisher Site | Google Scholar
  13. B. Abbas, A. A. Al-Qarawi, and A. Al-Hawas, “The ethnoveterinary knowledge and practice of traditional healers in Qassim region, Saudi Arabia,” Journal of Arid Environments, vol. 50, no. 3, pp. 367–379, 2002. View at: Publisher Site | Google Scholar
  14. J. R. S. Tabuti, S. S. Dhillion, and K. A. Lye, “Ethnoveterinary medicines for cattle (Bos indicus) in Bulamogi county, Uganda: plant species and mode of use,” Journal of Ethnopharmacology, vol. 88, no. 2-3, pp. 279–286, 2003. View at: Publisher Site | Google Scholar
  15. W. Pearson, “Ethnoveterinary medicine: the science of botanicals in equine health and disease,” in Proceedings of the 2nd European Equine Nutrition & Health Congress, Lelystad, The Netherlands, March 2004. View at: Google Scholar
  16. G. Muhammad, M. Z. Khan, M. H. Hussain, Z. Iqbal, M. Iqbal, and M. Athar, “Ethnoveterinary practices of owners of pneumatic-cart pulling camels in Faisalabad City (Pakistan),” Journal of Ethnopharmacology, vol. 97, no. 2, pp. 241–246, 2005. View at: Publisher Site | Google Scholar
  17. S. Mitra and S. K. Mukherjee, “Plants used as ethnoveterinary medicine in Uttar and Dakshin Dinajpur Districts of West Bengal, India,” in Advances in Ethnobotany, A. P. Das and A. K. Pandey, Eds., pp. 117–122, Bishen Singh Mahendra Pal Singh, Dehra Dun, India, 2007. View at: Google Scholar
  18. A. Pieroni, M. E. Giusti, C. de Pasquale et al., “Circum-Mediterranean cultural heritage and medicinal plant uses in traditional animal healthcare: a field survey in eight selected areas within the RUBIA project,” Journal of Ethnobiology and Ethnomedicine, vol. 2, article no. 16, 2006. View at: Publisher Site | Google Scholar
  19. J. T. Gradé, Ethnoveterinary knowledge in pastoral Karamoja, northern Uganda, Ph.D. thesis, Faculty of Bioscience Engineering, Ghent University, 2008.
  20. J. Gradé, R. Weladji, J. Tabuti, and P. Van Damme, “Healer-driven ethnoveterinary knowledge diffusion among semi-nomadic pastoralists in Karamoja, Uganda,” Afrika Focus, vol. 22, pp. 57–75, 2009. View at: Google Scholar
  21. D. R. Katerere and D. Luseba, Ethnoveterinary Botanical Medicine. Herbal Medicines for Animal Health, CRC Press, Boca Raton, Fla, USA, 2010.
  22. P. C. Phondani, R. K. Maikhuri, and C. P. Kala, “Ethnoveterinary uses of medicinal plants among traditional herbal healers in Alaknanda catchment of Uttarakhand, India,” African Journal of Traditional, Complementary and Alternative Medicines, vol. 7, no. 3, pp. 195–206, 2010. View at: Google Scholar
  23. G. J. Martinez and M. C. Lujan, “Medicinal plants used for traditional veterinary in the Sierras de Cordoba (Argentina): an ethnobotanical comparison with human medicinal uses,” Journal of Ethnobiology and Ethnomedicine, vol. 7, article 23, 2011. View at: Publisher Site | Google Scholar
  24. D. Mishra, “Ethnoveterinary Practices and use of herbal medicines for treatment of skin diseases in cattle: a study in Polsara Block, Ganjam District, Orissa, India,” Veterinary World, vol. 4, pp. 250–253, 2011. View at: Google Scholar
  25. N. V. Offiah, S. Makama, I. L. Elisha et al., “Ethnobotanical survey of medicinal plants used in the treatment of animal diarrhoea in Plateau State, Nigeria,” BMC Veterinary Research, vol. 7, article 36, 2011. View at: Publisher Site | Google Scholar
  26. A. M. Brisebarre, “Tradition and modernity: French shepherds’ use of medicinal bouquets,” in Ethnoveterinary Research and Development, C. M. McCorkle, E. Mathias, and T. W. Schillhorn Van Veen, Eds., pp. 76–90, Intermediate Technology Publications, London, UK, 1996. View at: Google Scholar
  27. Z. Iqbal and A. Jabbar, “Inventory of traditional veterinary botanicals from around the world,” in Ethnoveterinary Botanical Medicine. Herbal Medicines for Animal Health, D. R. Katerere and D. Luseba, Eds., pp. 125–164, CRC Press, Boca Raton, Fla, USA, 2010. View at: Google Scholar
  28. M. Pardo-de-Santayana, A. Pieroni, and R. K. Puri, Eds., Ethnobotany in the New Europe. People, Health and Wild Plant Resources, Berghahn Books, Oxford, UK, 2010.
  29. A. Pieroni, Ed., Herbs, Humans and Animals / Erbe, uomini e bestie, Experiences, Köln, Germany, 1999.
  30. L. Viegi, A. Pieroni, P. M. Guarrera, and R. Vangelisti, “A review of plants used in folk veterinary medicine in Italy as basis for a databank,” Journal of Ethnopharmacology, vol. 89, no. 2-3, pp. 221–244, 2003. View at: Publisher Site | Google Scholar
  31. M. A. Bonet and J. Vallès, “Ethnobotany of Montseny biosphere reserve (Catalonia, Iberian Peninsula): plants used in veterinary medicine,” Journal of Ethnopharmacology, vol. 110, no. 1, pp. 130–147, 2007. View at: Publisher Site | Google Scholar
  32. A. Belda, J. E. Martínez-Pérez, C. Martín, V. Peiró, and E. Seva, “Plants used to capture and sustain wild finches (Fringillidae) in southeast Spain,” Economic Botany, vol. 64, no. 4, pp. 367–373, 2010. View at: Publisher Site | Google Scholar
  33. S. Akerreta, M. I. Calvo, and R. Y. Cavero, “Ethnoveterinary knowledge in Navarra (Iberian Peninsula),” Journal of Ethnopharmacology, vol. 130, no. 2, pp. 369–378, 2010. View at: Publisher Site | Google Scholar
  34. G. Benítez, M. R. González-Tejero, and J. Molero-Mesa, “Knowledge of ethnoveterinary medicine in the Province of Granada, Andalusia, Spain,” Journal of Ethnopharmacology, vol. 139, no. 2, pp. 429–439, 2012. View at: Publisher Site | Google Scholar
  35. J. A. González, M. García-Barriuso, and F. Amich, “Ethnoveterinary medicine in the Arribes del Duero, western Spain,” Veterinary Research Communications, vol. 35, no. 5, pp. 283–310, 2011. View at: Publisher Site | Google Scholar
  36. A. Agelet and J. Vallès, “Vascular plants used in ethnoveterinary in Pallars (Pyrenees, Catalonia, Iberian Peninsula),” in Herbs, Humans and Animals / Erbe, uomini e bestie, A. Pieroni, Ed., pp. 14–35, Experiences, Köln, Germany, 1999. View at: Google Scholar
  37. M. Rigat, M. A. Bonet, S. Garcia, T. Garnatje, and J. Vallés, “Ethnobotany of food plants in the high river Ter valley (Pyrenees, Catalonia, Iberian Peninsula): non-crop food vascular plants and crop food plants with medicinal properties,” Ecology of Food and Nutrition, vol. 48, no. 4, pp. 303–326, 2009. View at: Publisher Site | Google Scholar
  38. M. Parada, E. Carrió, and J. Vallès, “Ethnobotany of food plants in the Alt Empordà region (Catalonia, Iberian peninsula),” Journal of Applied Botany and Food Quality, vol. 84, no. 1, pp. 11–25, 2011. View at: Google Scholar
  39. M. Rigat, T. Garnatje, and J. Vallès, “Plant biodiversity in Pyrenean homegardens (Catalonia, Iberian peninsula): current state of a mountain agroecosystem,” Acta Botanica Gallica, vol. 158, pp. 51–75, 2011. View at: Google Scholar
  40. M. Torres, Antropologia d’Eivissa i Formentera. Herbes, pastors, ses matances, Editorial Mediterrània, 1999.
  41. E. Carrió, M. Mayans, and J. Vallès, “Abans que es pins facin magranes i ses figueres melons. Primeres dades de dues recerques etnobotàniques a Formentera i Mallorca,” Mètode, vol. 72, pp. 19–22, 2011. View at: Google Scholar
  42. SMC (Meteorological Service of Catalonia), “Generalitat de Catalunya,” 2011, http://www.meteo.cat/. View at: Google Scholar
  43. R. Folch, La vegetació dels Països Catalans, Editorial Ketres, Barcelona, Spain, 2nd edition, 1986.
  44. J. Vigo, L’alta muntanya catalana. Flora i vegetació, Institut d’Estudis Catalans & Centre Excursionista de Catalunya, Barcelona, Spain, 2nd edition, 2010.
  45. IBESTAT (Balearic Islands Statistical Institute), “Govern de les Illes Balears,” 2012, http://www.ibestat.cat/. View at: Google Scholar
  46. AEMET (Meteorological National Agency), “Ministerio de Agricultura, Alimentación y Medio Ambiente, Spain,” 2011, http://www.aemet.es/. View at: Google Scholar
  47. L. Llorens, L. Gil, and F. J. Tébar, La vegetació de l’illa de Mallorca: bases per a la interpretació i gestió d’hàbitats, Associació Jardí Botànic de Palma, Palma de Mallorca, Spain, 2007.
  48. INE (Statistical National Institute), Spain, 2011, http://www.ine.es/.
  49. J. J. Pujadas, D. Comas, and J. Roca, Etnografia, Universitat Oberta de Catalunya, Barcelona, Spain, 2004.
  50. U. P. de Albuquerque, R. Farias Paiva de Lucena, and L. V. Fernandes Cruz da Cunha, Métodos e Técnicas na Pesquisa Etnobotánica, Comunigraf Editora & NUPEEA, Recife, Brazil, 2nd edition, 2008.
  51. J. M. Nolan and N. J. Turner, “Ethnobotany: the study of people - plants relationships,” in Ethnobiology, E. N. Anderson, D. M. Pearsall, E. S. Hunn, and N. L. Turner, Eds., pp. 133–147, John Wiley & Sons, Hoboken, NJ, USA, 2011. View at: Google Scholar
  52. O. de Bolòs and J. Vigo, Flora dels Països Catalans, vol. 4, Editorial Barcino, Barcelona, Spain, 2001.
  53. O. de Bolòs, J. Vigo, R. M. Masalles, and J. M. Ninot, Flora manual dels Països Catalans, Ed. Pòrtic, Barcelona, Spain, 3rd edition, 2005.
  54. P. Fournier, Flore illustrée des jardins et des parcs. Arbres, arbustes et fleurs de pleine terre, vol. 1–3, Paul Lechevalier éditeur, Paris, France, 1953.
  55. E. Sánchez-Monge, Flora Agricola. Taxonomía de las Magnoliofitas (Angiospermas) de interés agrícola, con excepción de las de aprovechamiento exclusivamente ornamental o forestal, vol. 2, Ministerio de Agricultura, Pesca y Alimentación, Madrid, Spain, 1991.
  56. E. Carrió, M. Parada, J. Parada et al., “Towards a database on ethnobotany of the Catalan linguistic area,” in Proceedings of the 11th Congress of the International Society for Ethnopharmacology (ISE '10), Albacete, Spain, September 2010. View at: Google Scholar
  57. R. Portères, Cours d‘Ethno-botanique et Ethno-zoologie (1969-1970). Volume I, Ethno-botanique générale, Muséum National d‘Histoire Naturelle (Laboratoire d‘Ethno-botanique et Ethno-zoologie), Faculté des Lettres (Institut d’Ethnologie), Paris, France, 1970.
  58. R. T. Trotter and M. H. Logan, “Informant consensus: a new approach for identifying potentially effective medicinal plants,” in Plants in Indigenous Medicine and Diet, Behavioural Approaches, N. L. Etkin, Ed., pp. 91–112, Redgrave Publishing Company, Bredford Hills, NY, USA, 1986. View at: Google Scholar
  59. J. Tardío and M. Pardo-de-Santayana, “Cultural importance indices: a comparative analysis based on the useful wild plants of southern Cantabria (northern Spain),” Economic Botany, vol. 62, no. 1, pp. 24–39, 2008. View at: Publisher Site | Google Scholar
  60. M. Höft, S. K. Barik, and A. M. Lykke, “Quantitative ethnobotany. Applications of multivariate and statistical analyses in ethnobotany,” in People and Plants Working Paper 6, UNESCO, Paris, France, 1999. View at: Google Scholar
  61. “The R Project for Statistical Computing,” 2011, http://www.r-project.com. View at: Google Scholar
  62. F. Ruskey and M. Weston, “A survey of Venn Diagrams,” The Electronic Journal of Combinatorics, 2005, http://www.combinatorics.org/Surveys/ds5/VennEJC.html. View at: Google Scholar
  63. L. Villar, J. M. Palacín, C. Calvo, D. Gómez, and G. Montserrat, Plantas medicinales del Pirineo aragonés y demás tierras oscenses, Consejo Superior de Investigaciones Científicas, Diputación de Huesca, Huesca, Spain, 1987.
  64. P. J. Houghton and I. M. Osibogun, “Flowering plants used against snakebite,” Journal of Ethnopharmacology, vol. 39, no. 1, pp. 1–29, 1993. View at: Google Scholar
  65. F. Ertug, “Plant, animal and human relationships in the folk medicine of Turkey,” in Herbs, Humans and Animals / Erbe, uomini e bestie, A. Pieroni, Ed., pp. 46–63, Experiences, Köln, Germany, 1999. View at: Google Scholar
  66. M. Parada, E. Carrió, M. A. Bonet, and J. Vallès, “Ethnobotany of the Alt Empordà region (Catalonia, Iberian Peninsula). Plants used in human traditional medicine,” Journal of Ethnopharmacology, vol. 124, no. 3, pp. 609–618, 2009. View at: Publisher Site | Google Scholar
  67. T. Johns, J. O. Kokwaro, and E. K. Kimanani, “Herbal remedies of the Luo of Siaya District, Kenya: establishing quantitative criteria for consensus,” Economic Botany, vol. 44, no. 3, pp. 369–381, 1990. View at: Publisher Site | Google Scholar
  68. M. R. González-Tejero, M. Casares-Porcel, C. P. Sánchez-Rojas et al., “Medicinal plants in the Mediterranean area: synthesis of the results of the project Rubia,” Journal of Ethnopharmacology, vol. 116, no. 2, pp. 341–357, 2008. View at: Publisher Site | Google Scholar
  69. V. Reyes-García, S. Vila, L. Aceituno-Mata et al., “Gendered homegardens: a study in three mountain areas of the Iberian Peninsula,” Economic Botany, vol. 64, no. 3, pp. 235–247, 2010. View at: Publisher Site | Google Scholar
  70. P. Font Quer, Plantas medicinales. El Dioscórides renovado, Editorial Labor, Barcelona, Catalonia, Spain, 1961.
  71. M. Rigat, M. A. Bonet, S. Garcia, T. Garnatje, and J. Vallès, “Studies on pharmaceutical ethnobotany in the high river Ter valley (Pyrenees, Catalonia, Iberian Peninsula),” Journal of Ethnopharmacology, vol. 113, no. 2, pp. 267–277, 2007. View at: Publisher Site | Google Scholar
  72. E. Carrió, Contribució al coneixement etnobotànic de Mallorca, M.S. thesis, Universitat de Barcelona, 2008.
  73. Y. Desco and L. Mas, “Estadístiques bàsiques de l’agricultura, la ramaderia i la pesca a les Illes Balears,” Secció d’Estadística de la Conselleria d’Agricultura, Medi Ambient i Territori, Govern de les Illes Balears, 2010. View at: Google Scholar
  74. E. Carrió and J. Vallès, “Ethnobotany of medicinal plants used in Eastern Mallorca (Balearic Islands, Mediterranean Sea),” Journal of Ethnopharmacology, vol. 141, no. 3, pp. 1021–1040, 2012. View at: Google Scholar
  75. S. Akerreta, R. Y. Cavero, and M. I. Calvo, “First comprehensive contribution to medical ethnobotany of Western Pyrenees,” Journal of Ethnobiology and Ethnomedicine, vol. 3, article no. 26, 2007. View at: Publisher Site | Google Scholar
  76. M. Heinrich, A. Ankli, B. Frei, C. Weimann, and O. Sticher, “Medicinal plants in Mexico: Healers' consensus and cultural importance,” Social Science and Medicine, vol. 47, no. 11, pp. 1859–1871, 1998. View at: Publisher Site | Google Scholar
  77. M. Leonti, H. Vibrans, O. Sticher, and M. Heinrich, “Ethnopharmacology of the Popoluca, Mexico: an evaluation,” Journal of Pharmacy and Pharmacology, vol. 53, no. 12, pp. 1653–1669, 2001. View at: Publisher Site | Google Scholar
  78. S. Ragupathy, N. G. Steven, M. Maruthakkutti, B. Velusamy, and M. M. Ul-Huda, “Consensus of the 'Malasars' traditional aboriginal knowledge of medicinal plants in the Velliangiri holy hills, India,” Journal of Ethnobiology and Ethnomedicine, vol. 4, article no. 8, 2008. View at: Publisher Site | Google Scholar
  79. L. Gil Vives and L. Llorens García, “Biogeographical analysis of the flora of Formentera (Balearic Island, Spain),” Lazaroa, vol. 25, pp. 169–178, 2004. View at: Google Scholar
  80. L. Garcías, “Contribució a la flora balear (I-IV, IX). Plantes dels voltants d’Artà i Capdepera,” Butlletí de la Institució Catalana d’Història Natural, 1905 – 1949. View at: Google Scholar
  81. IDESCAT (Catalonia Statistical Institute), “Generalitat de Catalunya,” 2012, http://www.idescat.cat/. View at: Google Scholar
  82. T. V. Asseldonk, “Ethnoveterinary medical practice in the European Union (EU). A case study of the Netherlands,” in Ethnoveterinary Botanical Medicine. Herbal Medicines for Animal Health, D. R. Katerere and D. Luseba, Eds., pp. 373–387, CRC Press, Boca Raton, Fla, USA, 2010. View at: Google Scholar

Copyright © 2012 Esperança Carrió 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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