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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Ecol. Evol.</journal-id>
<journal-title>Frontiers in Ecology and Evolution</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Ecol. Evol.</abbrev-journal-title>
<issn pub-type="epub">2296-701X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fevo.2017.00111</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Ecology and Evolution</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Firewood Resource Management in Different Landscapes in NW Patagonia</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Morales</surname> <given-names>Daniela V.</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/396465/overview"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Molares</surname> <given-names>Soledad</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/474851/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Ladio</surname> <given-names>Ana H.</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="author-notes" rid="fn001"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/367875/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Centro de Investigaci&#x000F3;n Esquel de Monta&#x000F1;a y Estepa patag&#x000F3;nica, CONICET Universidad Nacional de la Patagonia San Juan Bosco</institution> <country>Esquel, Argentina</country></aff>
<aff id="aff2"><sup>2</sup><institution>Instituto Nacional de Investigaciones en Biodiversidad y Medio Ambiente, CONICET Universidad Nacional del Comahue</institution> <country>S.C. de Bariloche, Argentina</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited by: Urs Feller, University of Bern, Switzerland</p></fn>
<fn fn-type="edited-by"><p>Reviewed by: Andrey S. Zaitsev, Justus Liebig Universit&#x000E4;t Gie&#x000DF;en, Germany; Milton Kanashiro, Embrapa Amazonia Oriental (Embrapa Easter Amazon), Brazil</p></fn>
<fn fn-type="corresp" id="fn001"><p>&#x0002A;Correspondence: Ana H. Ladio <email>ahladio&#x00040;gmail.com</email></p></fn>
<fn fn-type="other" id="fn002"><p>This article was submitted to Agroecology and Land Use Systems, a section of the journal Frontiers in Ecology and Evolution</p></fn></author-notes>
<pub-date pub-type="epub">
<day>15</day>
<month>09</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="collection">
<year>2017</year>
</pub-date>
<volume>5</volume>
<elocation-id>111</elocation-id>
<history>
<date date-type="received">
<day>23</day>
<month>06</month>
<year>2017</year>
</date>
<date date-type="accepted">
<day>01</day>
<month>09</month>
<year>2017</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2017 Morales, Molares and Ladio.</copyright-statement>
<copyright-year>2017</copyright-year>
<copyright-holder>Morales, Molares and Ladio</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p></license>
</permissions>
<abstract><p>Ecosystems, their components, processes and functions are all subject to management by human populations, with the purpose of adapting the environments to make them more habitable and ensuring the availability and continuity of subsistence resources. Although a lot of work has been carried out on resources of alimentary or medicinal interest, little has been done on associating processes of domestication with firewood extraction, a practice considered to be destructive of the environment. In the arid steppe of NW Patagonia, inhabited and managed for different purposes for a long time by Mapuche-Tehuelche communities, the gathering of combustible plant species has up to the present time played a crucial role in cooking and heating, and work is required to achieve sustainability of this resource. In this study we evaluate whether environments with less landscape domestication are more intensively used for firewood gathering. Using an ethnobiological approach, information was obtained through participant observation, interviews and free listing. The data were examined using both qualitative and quantitative approaches. Twenty-eight firewood species are gathered, both native (75%) and exotic (25%). The supply of firewood mainly depends on gathering from the domesticated (10 species), semi-domesticated (17 species) and low human intervention landscapes (17 species). In contrast to our hypothesis, average use intensity is similar in all these landscapes despite their different levels of domestication. That is, the different areas are taken advantage of in a complementary manner in order to satisfy the domestic demand for firewood. Neither do biogeographic origin or utilitarian versatility of collected plants vary significantly between the different landscape levels of domestication. Our results show that human landscape domestication for the provision of firewood seems to be a socio-cultural resilient practice, and shed new light on the role of culture in resource management. This approach may offer new tools for the development of firewood and cultural landscape management, and conservation planning.</p></abstract>
<kwd-group>
<kwd>gathering practices</kwd>
<kwd>socio-cultural resilience</kwd>
<kwd>complementarity</kwd>
<kwd>management</kwd>
</kwd-group>
<contract-num rid="cn001">PIP 0466</contract-num>
<contract-sponsor id="cn001">Consejo Nacional de Investigaciones Cient&#x000ED;ficas y T&#x000E9;cnicas<named-content content-type="fundref-id">10.13039/501100002923</named-content></contract-sponsor>
<counts>
<fig-count count="6"/>
<table-count count="3"/>
<equation-count count="0"/>
<ref-count count="74"/>
<page-count count="13"/>
<word-count count="10255"/>
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</front>
<body>
<sec sec-type="intro" id="s1">
<title>Introduction</title>
<p>Ecosystems, their components, processes and functions are all subject to transformation or management by local populations. Traditional ecological management is understood to be a set of interventions and transformations which are the result of community decisions regarding the natural and artificial systems, with the explicit purpose of adapting the landscape to make it more habitable and ensuring the availability of certain natural resources (Casas et al., <xref ref-type="bibr" rid="B21">2014</xref>). According to Toledo et al. (<xref ref-type="bibr" rid="B72">2003</xref>), resource management is an adaptive response to the uncertainty of their availability. It is part of the human desire to domesticate or control whatever is affected by this condition of uncertainty, so as to ensure the continuation of social and cultural life (Blancas et al., <xref ref-type="bibr" rid="B11">2014</xref>).</p>
<p>The subject of landscapes as biocultural systems has been studied widely over recent years (Berkes et al., <xref ref-type="bibr" rid="B9">2000</xref>; Miller and Davidson-Hunt, <xref ref-type="bibr" rid="B56">2010</xref>; Casas et al., <xref ref-type="bibr" rid="B21">2014</xref>; Lins Neto et al., <xref ref-type="bibr" rid="B52">2014</xref>). They are considered as physical spaces which reflect the use, values, learning and cosmovisions of the societies inhabiting them over time (Capparelli et al., <xref ref-type="bibr" rid="B15">2011</xref>; Castro et al., <xref ref-type="bibr" rid="B24">2012</xref>), and they also acquire a symbolic character as they are accorded significance by the different cultures (Greider and Garkovich, <xref ref-type="bibr" rid="B37">1994</xref>; Boillat et al., <xref ref-type="bibr" rid="B12">2013</xref>; Fern&#x000E1;ndez-Llamazares et al., <xref ref-type="bibr" rid="B36">2016</xref>).</p>
<p>The landscapes have been, and still are, constantly changed by their human inhabitants, leading to processes of domestication through both individual and collective subsistence practices which are reproduced and recreated in a dynamic way. This leads to socio-environmental constructions impregnated with everyday experience, in a permanent state of adaptation to the surroundings and their changing conditions (Berkes and Davidson-Hunt, <xref ref-type="bibr" rid="B10">2006</xref>; Haber, <xref ref-type="bibr" rid="B39">2006</xref>; Kareiva et al., <xref ref-type="bibr" rid="B43">2007</xref>; Castro et al., <xref ref-type="bibr" rid="B24">2012</xref>; Lema, <xref ref-type="bibr" rid="B51">2014</xref>). It is currently considered that the study of these practices in contexts that have undergone processes of change represents a key way of understanding the value of resources and their potential conservation (Washington, <xref ref-type="bibr" rid="B73">2013</xref>; Blancas et al., <xref ref-type="bibr" rid="B11">2014</xref>).</p>
<p>Local strategies for managing certain space-time resources depend on perception of which resources are useful and can be taken advantage of and preserved, and which are not, according to the necessities and perspectives arising over time among the population (Blancas et al., <xref ref-type="bibr" rid="B11">2014</xref>). Shaanker et al. (<xref ref-type="bibr" rid="B68">2003</xref>) highlight that locals&#x00027; ecological knowledge may have important implications for the long term conservation of plant resources, and that communities with a greater degree of this knowledge might be more &#x0201C;prudent&#x0201D; in their use of the environment, through adoption of less destructive harvesting practices, particularly when economic interests are affected, and even when being &#x0201C;prudent&#x0201D; implies poorer short term returns.</p>
<p>The study of the body of fuelwood knowledge which forms part of the accumulative cultural heritage of local communities, referred to conceptually as traditional ecological knowledge (TEK) (Berkes et al., <xref ref-type="bibr" rid="B9">2000</xref>), may contribute to the construction of perspectives on the sustainable management of these ecosystems. This involves in-depth study of the knowledge and practices associated with use of the environment, which are related to the maintenance of ecological cycles, and therefore ensure sustainability, thus making possible the coexistence and even the evolution of inhabitants along with their natural resources (Berkes et al., <xref ref-type="bibr" rid="B9">2000</xref>; Shaanker et al., <xref ref-type="bibr" rid="B68">2003</xref>; Berkes, <xref ref-type="bibr" rid="B8">2004</xref>; Tiwari et al., <xref ref-type="bibr" rid="B71">2010</xref>). Despite the progress made in this subject with regard to the use of firewood (Cardoso et al., <xref ref-type="bibr" rid="B18">2012</xref>, <xref ref-type="bibr" rid="B17">2015</xref>; Arre et al., <xref ref-type="bibr" rid="B6">2015</xref>; Morales et al., <xref ref-type="bibr" rid="B60">2017</xref>), the processes associated with domestication of the arid cultural landscape leading to the promotion and supply of these scarce resources are still unknown. The studies refer mainly to firewood extraction as a destructive practice that shows little care for the environment or resource renewal (Tabuti, <xref ref-type="bibr" rid="B69">2007</xref>).</p>
<p>Among the practices of anthropization of the environment, the <italic>ex</italic> and <italic>in situ</italic> management of vegetation (Casas et al., <xref ref-type="bibr" rid="B22">2007</xref>, <xref ref-type="bibr" rid="B23">2008</xref>, <xref ref-type="bibr" rid="B21">2014</xref>; Lins Neto et al., <xref ref-type="bibr" rid="B52">2014</xref>), control of ecological succession, diversion of watercourses and the gathering of useful plants (Davidson-Hunt and Berkes, <xref ref-type="bibr" rid="B31">2003</xref>; Molares and Ladio, <xref ref-type="bibr" rid="B57">2009</xref>; Pirondo and Keller, <xref ref-type="bibr" rid="B62">2014</xref>), have been mentioned as strategies which increase the supply of species of interest and reduce the uncertainty of their availability throughout the year and in succeeding years (Barrera-Bassols and Toledo, <xref ref-type="bibr" rid="B7">2005</xref>; Molares and Ladio, <xref ref-type="bibr" rid="B57">2009</xref>). For example, taking advantage of ruderal and exotic species that appear rapidly on land where clearings have been produced by disturbances of moderate intensity is a practice shared by many cultures (Molares and Ladio, <xref ref-type="bibr" rid="B59">2014</xref>).</p>
<p>The species diversity constructed through different management practices may be taken advantage of in different ways, utilitarian versatility being considered as the sum of the different uses presented by a certain resource. It has been found that the species with highest use consensus in these societies often present high utilitarian versatility, a pattern based on profound knowledge of the best-known species, which promotes caring attitudes, since the people value the potential of the species in a holistic way (Richeri et al., <xref ref-type="bibr" rid="B65">2013</xref>). Studies performed on medicinal plants have shown that plants native to a certain place generally offer greater use diversity than exotic species, due to the longer period of time they have been in contact with local populations (Molares and Ladio, <xref ref-type="bibr" rid="B57">2009</xref>).</p>
<p>Since ancient times indigenous communities in Patagonia have bonded with the resources in their environment, which has not only allowed them to develop a deep knowledge of nature, but has also favored the creation of diverse landscapes with different levels of domestication (Ladio and Molares, <xref ref-type="bibr" rid="B50">2014</xref>; Sedrez dos Reis et al., <xref ref-type="bibr" rid="B67">2014</xref>). These communities have viewed nature as a fundamental part of their life system. In particular, the Andean environment, across its entire altitudinal gradient, is taken advantage of as a source of natural resources through different gathering practices, although practices tending toward tolerance, facilitation and promotion are also observed (Ladio and Molares, <xref ref-type="bibr" rid="B50">2014</xref>), generating a gradient/continuum of landscapes with different levels of human intervention. These spaces were, and still are, valued differentially according to their vegetation and geomorphological characteristics, as well as their utilitarian and symbolic attributes (Ladio and Lozada, <xref ref-type="bibr" rid="B46">2003</xref>, <xref ref-type="bibr" rid="B47">2004</xref>; Ladio et al., <xref ref-type="bibr" rid="B48">2007</xref>).</p>
<p>The gathering of woody species for fire is a subject of great socioeconomic relevance on a global level (Tabuti et al., <xref ref-type="bibr" rid="B70">2003</xref>; Chettri and Sharma, <xref ref-type="bibr" rid="B26">2007</xref>; Ramos et al., <xref ref-type="bibr" rid="B64">2008</xref>) and as an area of study, considering the cultural value of heating by firewood, the severity of winter at this latitude, the scarcity of available petroleum-based alternatives, and their high cost (Cardoso et al., <xref ref-type="bibr" rid="B18">2012</xref>). As a result, most households, and the rural or semi-rural ones in particular, depend principally on plants for cooking and heating (Cardoso et al., <xref ref-type="bibr" rid="B18">2012</xref>; Arre et al., <xref ref-type="bibr" rid="B6">2015</xref>). Recent ethnobotanical studies in Patagonia have documented consumption patterns of firewood species, the attributes of the wood, and preferences shown by locals, oriented mainly toward native species (Cardoso et al., <xref ref-type="bibr" rid="B18">2012</xref>, <xref ref-type="bibr" rid="B19">2013</xref>, <xref ref-type="bibr" rid="B17">2015</xref>; Arre et al., <xref ref-type="bibr" rid="B6">2015</xref>) and the new practices employed to counteract scarcity of the firewood resource, such as the use of exotic species of more or less recent appearance in the region (Cardoso et al., <xref ref-type="bibr" rid="B20">2017</xref>). This evidence reflects constant processes of hybridization of knowledge, which make possible the incorporation of new woody elements to compensate for deficiencies (Cardoso and Ladio, <xref ref-type="bibr" rid="B16">2011</xref>).</p>
<p>The objectives of this work were to analyze the gathering patterns of firewood plants and their relationship with the different domesticated landscapes that form part of daily life in two rural communities of the Patagonian steppe. Our questions are: (1) whether environments with a lower level of landscape domestication are used more intensively for firewood gathering, in terms of species richness and use consensus. (2) whether in these environments with a lower level of landscape domestication a higher proportion of native species are gathered, and a higher number of species that were used in the past. (3) whether in these environments with a lower level of landscape domestication the woody species are used in a more versatile way.</p>
</sec>
<sec sec-type="materials and methods" id="s2">
<title>Materials and methods</title>
<sec>
<title>Study area</title>
<p>The study area takes in the communities of Gualjaina (42&#x000B0;4&#x02032;S and 70&#x000B0;32&#x02032;W) and Paraje Costa del Lep&#x000E1; (42&#x000B0;34&#x02032;S and 71&#x000B0;03&#x02032;W), in the northwest of Chubut province, Argentina (Figure <xref ref-type="fig" rid="F1">1</xref>). They are neighboring communities, approximately 15 km apart, and have close links in terms of family, lifestyle and work, among other factors. The area is located in the Central Plateau Region, in the Lep&#x000E1; and Gualjaina river basins, at an altitude of between 545 and 760 m.a.s.l.</p>
<fig id="F1" position="float">
<label>Figure 1</label>
<caption><p>Location of the study area in NW Chubut province, Argentina.</p></caption>
<graphic xlink:href="fevo-05-00111-g0001.tif"/>
</fig>
<p>These communities are located in environments dominated by grass-shrub steppe. The predominant species are <italic>Mulynum spinosum</italic> (Cav). Pers., <italic>Senecio filaginoides</italic> DC., <italic>Nassauvia axillaris</italic> (Lag. ex Lindl.) D. Don., <italic>Berberis mycrophilla</italic> G. Forst., and <italic>Schinus johnstonii</italic> F.A. Barkley. This area corresponds to the phytogeographical region of Patagonian Province, Central District (Cabrera, <xref ref-type="bibr" rid="B14">1976</xref>).</p>
<p>The climate is dry and cool. Annual average precipitation of 119 mm, mainly concentrated between May and September, with annual temperatures of 17.5&#x000B0;C in summer and 2.6&#x000B0;C in winter; dominant winds are from the west (Mereb, <xref ref-type="bibr" rid="B55">1990</xref>).</p>
<p>Gualjaina has an estimated population of 1183 inhabitants and a total population of 2,500 people including the 17 smaller communities (one of these is Costa de Lep&#x000E1;) that have formed close to it, and it covers an area of ca. 2,870 km<sup>2</sup>, based on the population census of 2010 (Instituto Nacional de Estad&#x000ED;stica y Censos, <xref ref-type="bibr" rid="B41">2010</xref>). In this region a proportion of the population live in the town, while other residents are distributed along the edges of rivers or in rural areas. Most people are descendants of Mapuches and Creoles (ECPI, <xref ref-type="bibr" rid="B33">2007</xref>). There are some institutions in the communities, such as police, hospital, school and some churches (Catholic and Evangelical). In addition, some national institutions from outside the community work in the area (National Institute for Agricultural Technology; Development Corporation of Chubut province). They have provided technical assistance and exotic plant seeds with agricultural uses. The main economic activity is based on livestock breeding and to a lesser degree, agriculture, handcraft sales, commerce, tourism, and some people are supported by social assistance from the state. Firewood is the most significant fuel in these communities, many of which employ it for domestic use, as they have no access to gas.</p>
</sec>
<sec>
<title>Data collection</title>
<p>Fieldwork for this study was carried out between February and November 2015. A total of 33 household heads consented to participate in the interviews. Each person was asked to sign the Free and Clarified Consent Form according to the Code of Ethics of the International Society of Ethnobiology (ISE, <xref ref-type="bibr" rid="B42">2006</xref>).</p>
<p>The adult population was composed of men and women ranging in age from 30 to 90, with a mean age of 59.8. The informants were selected at random, each one representing a household unit. Free listing was used to determine the composition and species richness of firewood plants known by each informant (Alburquerque et al., <xref ref-type="bibr" rid="B3">2010</xref>). In addition, open and semi-structured interviews were carried out in order to comprehend the landscape dynamic used to obtain firewood plants. We asked the local inhabitants about places for gathering firewood species (i.e., scrubland, cultivated land, areas close to water bodies). Furthermore, informants were consulted as to any additional uses of the firewood species named, strategies for acquiring them and the continuity of use of the species. Analysis of use continuity was based on the methodology proposed by Fern&#x000E1;ndez-Llamazares et al. (<xref ref-type="bibr" rid="B36">2016</xref>); participants were asked whether each firewood species mentioned had been used in the past and up to the present, or if it was used only in the past, or only in the present. The point of reference used to represent the past was the informant&#x00027;s childhood.</p>
<p>Data were supplemented using other ethnobotanical techniques, such as participant observation, in-depth interviews and field excursions with key informants in order to collect botanical material of the species cited in the interviews (Guber, <xref ref-type="bibr" rid="B38">2006</xref>). Samples of plants were herborized and placed in the Esquel Mountain and Patagonian Steppe Research Center. The botanical reference material was identified according to Correa (<xref ref-type="bibr" rid="B27">1971</xref>, <xref ref-type="bibr" rid="B28">1978</xref>, <xref ref-type="bibr" rid="B29">1984</xref>) and its scientific names were updated following Zuloaga and Morrone (<xref ref-type="bibr" rid="B74">1999</xref>) and International Plant Names Index (<ext-link ext-link-type="uri" xlink:href="http://www.ipni.org">www.ipni.org</ext-link>).</p>
</sec>
<sec>
<title>Data analysis</title>
<p>Composition and richness of species and botanical families were estimated using the total number of species mentioned by the Mapuche informants.</p>
<p>The biogeographic origin of species was classified according to the Darwinion Institute catalog of vascular plants (Zuloaga and Morrone, <xref ref-type="bibr" rid="B74">1999</xref>) and the following were considered as etic categories: native to Patagonia (indigenous species that grow approximately from 37&#x000B0; S southward) and exotic to Patagonia.</p>
<p>Use consensus (UC) was obtained considering the frequency of use citations for each species in the total population. It was calculated by dividing the number of informants (n) who used the species (i) by the total number of informants interviewed (<italic>N</italic> &#x0003D; 33) &#x000D7; 100, (ni/N &#x000D7; 100) (Molares and Ladio, <xref ref-type="bibr" rid="B58">2012</xref>). This index is used as an indirect measure of the importance of use of cited species.</p>
<p>The versatility of use of the species was estimated using the index: UVi &#x0003D; &#x02211; UVsi/ni (Phillips and Gentry, <xref ref-type="bibr" rid="B61">1993</xref>), where UVsi is the number of uses registered by informant i for species s, and ni is the number of people who mention species i. The values obtained were put into two categories: (1). Fuel use only; (2). Fuel use plus one or more additional uses (i.e., construction, fodder, medicinal, edible).</p>
<p>Acquisition strategies of firewood resources were classified etically as: gathering, purchase, exchange or state subsidies.</p>
<p>The landscape used for gathering wood was analyzed considering the different management processes used by the population and also the different signs of domestication. These local observations of the Mapuche landscape were then grouped into several etic categories listed further: Landscape with low human intervention: this was defined as the environment with lowest human influence or management (i.e., hills and plains with mainly grasses and low bushes, with scattered clumps of native shrubs approximately 1.50 m in height, all intertwined; extensive livestock grazing; no separation of areas or zoning of pastureland; no movement of land, or irrigation, and only scarce to moderate quantities of dung; located at a distance of no less than 3 km from human settlements). Semidomestic landscape: moderate human intervention (i.e., more signs and dung from animals than previous environment, and areas with bare soil; includes areas next to rivers, with small clumps of exotic species of <italic>Salix</italic> sp.; few, widely separated irrigation canals; temporary infrastructures such as cattle sheds; shelter from wind for the animals, constructed with corrugated iron, poles and tethering posts). Domestic landscape: has undergone the highest level of human intervention (i.e., around dwellings, where outbuildings are situated, corrals, gardens and other cultivated spaces such as vegetable gardens or small fruit and vegetable farms). The continuity of use of each woody species was categorized as: current use (i.e., the person has used it within the last year), past use (i.e., the species mentioned was used only in their infancy); current-past use (i.e., the same species continues to be used from the informant&#x00027;s infancy up to the present time).</p>
<p>For general analysis, the total richness of native and exotic species was compared using a binomial test (<italic>p</italic> &#x0003C; 0.05), and use consensus was calculated with the Mann Whitney <italic>U</italic>-test (<italic>p</italic> &#x0003C; 0.05).</p>
<p>The richness of firewood species in the different types of landscape was compared by means of the Chi-squared test (<italic>p</italic> &#x0003C; 0.05), and to compare the biogeographic origin and use versatility of the species gathered in each type of landscape the binomial test was used (<italic>p</italic> &#x0003C; 0.05). Species similarity between environments with different levels of domestication was analyzed using the Jaccard index (JI: c/ (a &#x0002B; b&#x0002B; c) &#x000D7; 100), where c is the number of species common to two environments, a is the number of unique species in environment A, and b is the number of unique species in environment B (H&#x000F6;ft et al., <xref ref-type="bibr" rid="B40">1999</xref>).</p>
<p>The UC of the species was compared for different types of landscape, according to the following categories: biogeographic origin, use versatility and continuity of use by means of the non-parametric Kruskall Wallis test (<italic>p</italic> &#x0003C; 0.05). In addition, for each landscape comparisons were made of UC in relation to versatility, using the Mann Whitney <italic>U</italic>-test (<italic>p</italic> &#x0003C; 0.05).Species richness was compared between the continuity of use classes using the Chi-squared test (<italic>p</italic> &#x0003C; 0.05).</p>
<p>In addition, a multinomial logistic regression analysis was carried out with the SPSS 22.0 program in order to complement the information and obtain a model to explain how the proportion of plants varies between the different levels of landscape domestication (dependent variable category) according to their biogeographic origin and use versatility (independent variable category) (Chan, <xref ref-type="bibr" rid="B25">2005</xref>; Ladio and Molares, <xref ref-type="bibr" rid="B49">2013</xref>). In this analysis we excluded the species obtained through purchase or subsidies (i.e., <italic>Nothofagus antarctica, Pinus</italic> spp.) and the variables (i.e., life form, continuity of use) that do not register as significant in the model. In this kind of regression, tendencies are established according to the categories under comparison; in this case, the domestic landscape. A description of the variables in the model and the distribution of all cases are shown in Table <xref ref-type="table" rid="T2">2</xref>. The model was found to be significant (<italic>p</italic> &#x0003C; 0.05). Calculations of the odds ratios (i.e., the probability of an event happening) are shown in Table <xref ref-type="table" rid="T3">3</xref> by means of e<sup>beta</sup> &#x0003D; Exp (B) (Chan, <xref ref-type="bibr" rid="B25">2005</xref>; Ladio and Molares, <xref ref-type="bibr" rid="B49">2013</xref>).</p>
</sec>
</sec>
<sec sec-type="results" id="s3">
<title>Results</title>
<sec>
<title>The role of firewood in the lives of costa de lep&#x000E1; and gualjaina inhabitants</title>
<p>Firewood plants provide the main fuel for heating and cooking for almost all households in Gualjaina and Costa del Lep&#x000E1; (100% of informants). The gathering and use of plants is an activity carried out by both men and women, all year round. Collection patterns consist of gathering (97% of informants) a mixture of dead and green wood for the purpose of long-lasting fires, or fallen pieces of wood in open wild areas, and pruned branches from forest plantations. The firewood is then transported in bundles carried on the shoulders, or the load is carried by an animal or by human-powered carts (Figure <xref ref-type="fig" rid="F2">2</xref>).</p>
<fig id="F2" position="float">
<label>Figure 2</label>
<caption><p>Gathering firewood of <italic>Salix</italic> sp., <italic>P. alba</italic> and a mixture of branches from different trees with human-powered carts in Costa del Lep&#x000E1;, Chubut.</p></caption>
<graphic xlink:href="fevo-05-00111-g0002.tif"/>
</fig>
<p>Approximately half the community complement firewood gathering with purchase (48%), and they mainly buy firewood from Sub-Antarctic forest such as <italic>N. antarctica</italic>. To a lesser extent (15%), locals are aided by government firewood programs called &#x0201C;the heat program&#x0201D; which provide home heating assistance in the form of 6 m<sup>3</sup> of firewood in winter, composed mainly of <italic>N. antarctica, Pinus</italic> spp., <italic>Salix</italic> sp. and <italic>Populus alba</italic>. The exchange of firewood for animals (3%) also takes place, both within the community and with neighboring communities.</p>
<p>In addition to the above, in some situations where wood is limited other fuel-types such as liquefied Petroleum Gas (LPG) and animal by-products, including dung from cows and sheep, are used. In general, people reported using LPG (82%) only for cooking or heating up water, due to its elevated cost.</p>
<p>The communities convey the important role that firewood plays in their culture; they do not simply view it in terms of meeting energy needs. The cooking stoves provide the highly appreciated space heating that allows families to sit around the fire and socialize. As well as this, the taste of some traditional meals is associated with the selection of firewood used in its preparation. For example, the embers of <italic>Nassauvia axillaris</italic> are used for cooking bread. In addition, according to informants, heating a home with firewood is healthier than using other forms of heating. However, for most informants the supply of firewood now and in the future is a constant source of worry, and they feel responsible for finding alternatives due to the current scarcity. As some locals commented: &#x0201C;<italic>the people always used to go out to collect firewood, now you don&#x00027;t see it so much&#x02026;&#x0201D;</italic>(D.A). &#x0201C;<italic>It&#x00027;s good that you folk who come from outside tell us what can be done to improve the situation, things that we don&#x00027;t realize&#x02026;</italic>&#x0201D;(E.O).</p>
</sec>
<sec>
<title>The gathering of native and exotic firewood plants</title>
<p><italic>Plant composition:</italic> Locals gather a total of 28 firewood species, belonging to 24 genera, and grouped into 14 families (Table <xref ref-type="table" rid="T1">1</xref>), of which Asteraceae (5 species) and Salicaceae (4 species) are the most collected. The most frequently collected species are the native <italic>S. johnstonii</italic> (use consensus of 78.8%) and <italic>N. axillaris</italic> (54.5%), and the exotic <italic>Salix</italic> sp. (87.9%) and <italic>P. alba</italic> (54.5%) (Table <xref ref-type="table" rid="T1">1</xref>). As expected, considering biogeographic origin and not taking into account the gathering environments they come from, or their different levels of domestication, the total richness of plants used as firewood was higher for native species (75%, 22 species), while exotic species accounted for 25% (6 species) (Binomial test, <italic>p</italic> &#x0003D; 0.02). However, it is notable that with respect to use consensus, inhabitants appear to use exotic species (27.3% &#x000B1; 14.6) more than native species (18.2% &#x000B1; 4), although this difference is not significant (Mann Whitney <italic>U</italic>-test, <italic>p</italic> &#x0003D; 0.97).</p>
<table-wrap position="float" id="T1">
<label>Table 1</label>
<caption><p>Firewood species used in the rural communities of Costa del Lep&#x000E1; and Gualjaina, in the Patagonia steppe.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>Scientific name</bold></th>
<th valign="top" align="left"><bold>Vernacular name</bold></th>
<th valign="top" align="left"><bold>Family</bold></th>
<th valign="top" align="left"><bold>Origin</bold></th>
<th valign="top" align="left"><bold>UC (%)</bold></th>
<th valign="top" align="left"><bold>Firewood acquisition strategies</bold></th>
<th valign="top" align="left"><bold>Degree of domestication</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left"><italic>Salix</italic> sp.</td>
<td valign="top" align="left">Sauce</td>
<td valign="top" align="left">Salicaceae</td>
<td valign="top" align="left">E</td>
<td valign="top" align="left">87.9</td>
<td valign="top" align="left">Gathering. Purchase. Firewood programs. Exchange.</td>
<td valign="top" align="left">Semi-domestic. Domestic</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Schinus johnstonii</italic> F.A. Barkley.</td>
<td valign="top" align="left">Molle</td>
<td valign="top" align="left">Anacardiaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">78.8</td>
<td valign="top" align="left">Gathering. Exchange.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Populus alba</italic> L.</td>
<td valign="top" align="left">Alamo plateado</td>
<td valign="top" align="left">Salicaceae</td>
<td valign="top" align="left">E</td>
<td valign="top" align="left">54.5</td>
<td valign="top" align="left">Gathering. Purchase. Firewood programs. Exchange.</td>
<td valign="top" align="left">Semi-domestic. Domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Nassauvia axillaris</italic> (Lag. ex Lindl.) D. Don</td>
<td valign="top" align="left">U&#x000F1;a de gato</td>
<td valign="top" align="left">Asteraceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">54.5</td>
<td valign="top" align="left">Gathering. Exchange.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Nothofagus antarctica</italic><xref ref-type="table-fn" rid="TN1"><sup>&#x0002A;</sup></xref> (G. Forst.) Oerst.</td>
<td valign="top" align="left">&#x000D1;ire</td>
<td valign="top" align="left">Nothofagaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">45.5</td>
<td valign="top" align="left">Purchase. Firewood programs.</td>
<td/>
</tr>
<tr>
<td valign="top" align="left"><italic>Corynabutilon bicolor</italic> (Phil. ex K. Schum.) Kearney</td>
<td valign="top" align="left">Monte moro</td>
<td valign="top" align="left">Malvaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">33.3</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Lycium</italic> sp.</td>
<td valign="top" align="left">Monte negro</td>
<td valign="top" align="left">Solanaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">27.3</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Berberis mycrophylla</italic> G. Forst.</td>
<td valign="top" align="left">Calafate</td>
<td valign="top" align="left">Berberidaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">27.3</td>
<td valign="top" align="left">Gathering. Exchange.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Senecio filaginoides</italic> DC</td>
<td valign="top" align="left">Charcao</td>
<td valign="top" align="left">Asteraceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">24.2</td>
<td valign="top" align="left">Gathering. Exchange.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic. Domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Stillingia patagonica</italic> (Speg.) Pax and K. Hoffm.</td>
<td valign="top" align="left">Mata perro</td>
<td valign="top" align="left">Euphorbiaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">24.2</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Ochetophila trinervis</italic> (Gillies ex Hook. and Arn.)</td>
<td valign="top" align="left">Chacai</td>
<td valign="top" align="left">Rhamnaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">21.2</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Baccharis salicifolia</italic> (Ruiz and Pav.) Pers.</td>
<td valign="top" align="left">Chilca</td>
<td valign="top" align="left">Asteraceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">18.2</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Chuquiraga avellanedae</italic> Lorentz</td>
<td valign="top" align="left">Trallao</td>
<td valign="top" align="left">Asteraceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">18.2</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic. Domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Prosopis denudans</italic> var. <italic>patagonica</italic> Benth. (Speg.) Burkart</td>
<td valign="top" align="left">Algarrobillo</td>
<td valign="top" align="left">Fabaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">15.2</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Retanilla patagonica</italic> (Speg.) Tortosa</td>
<td valign="top" align="left">Barba chivo</td>
<td valign="top" align="left">Rhamnaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">15.2</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Prunus cerasus</italic> L.</td>
<td valign="top" align="left">Guindo</td>
<td valign="top" align="left">Rosaceae</td>
<td valign="top" align="left">E</td>
<td valign="top" align="left">9.1</td>
<td valign="top" align="left">Gathering crop residues.</td>
<td valign="top" align="left">Domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Salix humboldtiana</italic> Willd.</td>
<td valign="top" align="left">Sauce com&#x000FA;n</td>
<td valign="top" align="left">Salicaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">9.1</td>
<td valign="top" align="left">Gathering. Purchase. Firewood programs.</td>
<td valign="top" align="left">Semi-domestic. Domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Adesmia volckmanni</italic> Phil.</td>
<td valign="top" align="left">Mamuel choique</td>
<td valign="top" align="left">Fabaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">6.1</td>
<td valign="top" align="left">Gathering. Exchange.</td>
<td valign="top" align="left">Low degree of human influence. Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Malus domestica</italic> Borkh.</td>
<td valign="top" align="left">Manzano</td>
<td valign="top" align="left">Rosaceae</td>
<td valign="top" align="left">E</td>
<td valign="top" align="left">6.1</td>
<td valign="top" align="left">Gathering crop residues.</td>
<td valign="top" align="left">Domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Azorela monantha</italic> Clos</td>
<td valign="top" align="left">Le&#x000F1;a de piedra</td>
<td valign="top" align="left">Apiaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">6.1</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Pinus</italic> ssp.<xref ref-type="table-fn" rid="TN1"><sup>&#x0002A;</sup></xref></td>
<td valign="top" align="left">Pino</td>
<td valign="top" align="left">Pinaceae</td>
<td valign="top" align="left">E</td>
<td valign="top" align="left">3.0</td>
<td valign="top" align="left">Firewood programs.</td>
<td/>
</tr>
<tr>
<td valign="top" align="left"><italic>Salix viminalis</italic> L.</td>
<td valign="top" align="left">Sauce mimbre</td>
<td valign="top" align="left">Salicaceae</td>
<td valign="top" align="left">E</td>
<td valign="top" align="left">3.0</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Schinus patagonicus</italic> (Phil.) I.M. Johnst. ex Cabrera.</td>
<td valign="top" align="left">Laura</td>
<td valign="top" align="left">Anacardiaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">3.0</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Semi-domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Atriplex lampa</italic> (Moq.) D. Dietr.</td>
<td valign="top" align="left">Sampa</td>
<td valign="top" align="left">Chenopodiaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">3.0</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Ephedra ochreata</italic> Miers</td>
<td valign="top" align="left">Silupe</td>
<td valign="top" align="left">Ephedraceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">3.0</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Fabiana imbricata</italic> Ruiz and Pav.</td>
<td valign="top" align="left">Palo piche</td>
<td valign="top" align="left">Solanaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">3.0</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Maihuenia patagonica</italic> (Phil.) Britton and Rose</td>
<td valign="top" align="left">Chupa sangre</td>
<td valign="top" align="left">Cactaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">3.0</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Mulinum spinosum</italic> (Cav.) Pers.</td>
<td valign="top" align="left">Neneo</td>
<td valign="top" align="left">Apiaceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">3.0</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Low degree of human influence.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Senecio</italic> sp.</td>
<td valign="top" align="left">Charcao</td>
<td valign="top" align="left">Asteraceae</td>
<td valign="top" align="left">N</td>
<td valign="top" align="left">3.0</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Domestic.</td>
</tr>
<tr>
<td valign="top" align="left"><italic>Ulmus minor</italic> Mill.</td>
<td valign="top" align="left">Olmo</td>
<td valign="top" align="left">Ulmaceae</td>
<td valign="top" align="left">E</td>
<td valign="top" align="left">3.0</td>
<td valign="top" align="left">Gathering.</td>
<td valign="top" align="left">Domestic</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><italic>UC, Use Consensus; N, Native; E, Exotic;</italic></p>
<fn id="TN1">
<label>&#x0002A;</label>
<p><italic>Non-local landscape plants</italic>.</p></fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec>
<title>Domesticated landscapes and firewood gathering</title>
<sec>
<title>Species richness according to the level of landscape domestication</title>
<p>The richness of firewood species is not higher in environments with less domestication, and does not vary significantly between different landscape categories (Chi-squared test <italic>p</italic> &#x0003D; 0.328) (Figure <xref ref-type="fig" rid="F3">3</xref>). The richness found in domestic landscapes is represented by 10 species, whereas in the semi-domestic and low intervention landscapes it is composed of 17 species.</p>
<fig id="F3" position="float">
<label>Figure 3</label>
<caption><p>Average richness of combustible species cited by inhabitants according to landscape categories (domestic, semi-domestic and low human intervention) and biogeographic origin. Key: &#x025A0; Native species; &#x025A0; Exotic species; &#x025A0; Total number. Different letters indicate significant differences.</p></caption>
<graphic xlink:href="fevo-05-00111-g0003.tif"/>
</fig>
<p>With regard to the similarity of woody species between different domesticated landscapes, the highest values were obtained for the low domestication and semidomestic landscapes (50% of the species). The domestic and semidomestic landscapes, meanwhile, showed only 13% similarity. No similarity whatsoever was found between the domestic and low intervention landscapes (0%).</p>
<p>Informants mentioned (19% of cites) that the domesticated landscapes, which have undergone most human intervention, are taken advantage of for both native and exotic firewood species (Binomial test, <italic>p</italic> &#x0003D; 0.75), of which a high proportion (60%, 6 species) are cultivated exotic species, while the remainder (40%) are native species (Figure <xref ref-type="fig" rid="F3">3</xref>). The most frequent species are <italic>P. alba</italic> and <italic>Salix</italic> sp.</p>
<p>The semi-domestic areas, made up of river valleys that run through the communities (rivers Gualjaina and Lep&#x000E1;, Figure <xref ref-type="fig" rid="F1">1</xref>) together with the wetlands (flood meadows and water holes), also represent areas recognized for their provision of firewood. Not only do locals find wood here for cutting, but also driftwood from the rivers, locally known as &#x0201C;resaque,&#x0201D; consisting of a mixture of native and exotic species, which may be used thanks to local knowledge of water pulses. From this landscape mostly native species are obtained (88%, 15 species) (Binomial test, <italic>p</italic> &#x0003D; 0.002) (Figure <xref ref-type="fig" rid="F3">3</xref>). The exotic species <italic>Salix</italic> sp. is the most collected.</p>
<p>The landscapes with least human intervention are also widely known and explored by locals, who reported frequenting them since they were children, when they would go out with their parents to gather firewood and do other activities such as checking on the herd. The highest proportion of inhabitants &#x02018;cites (47%) refers to the use of this environment, from which only native species are obtained (Figure <xref ref-type="fig" rid="F3">3</xref>). <italic>Schinus johnstonii</italic> is the most collected; according to informants its roots provide very good quality firewood. Nevertheless, they do show concern about its increasing scarcity, as it is slow growing and suffers great pressure of use.</p>
</sec>
<sec>
<title>Comparison between life forms</title>
<p>Most species used were shrubs (70%, 21 species), and were found mainly in semi-domestic and low human intervention landscapes, while trees (30%, 9 species) were found mostly near watercourses (semi-domestic) or cultivated by man as hedges, for wind protection and other uses in the domestic landscapes. <italic>N. antarctica</italic> and <italic>Pinus</italic> sp. are trees whose wood constitutes an important part of the firewood used by inhabitants; however, it is not obtained in the local landscape, but is purchased by the truckload or received through state aid programs.</p>
</sec>
<sec>
<title>Use consensus of species according to level of landscape domestication and biogeographic origin</title>
<p>The three types of landscape were used with the same intensity (Test de Kruskall-Wallis, <italic>p</italic> &#x0003D; 0.61). Interestingly, the domestic landscape presented a higher average UC (11.72% &#x000B1; 3.71) than both the semi-domestic landscape (10.75 &#x000B1; 2.49), and the landscape with least human intervention (8.52 &#x000B1; 1.78) (Figure <xref ref-type="fig" rid="F4">4</xref>).</p>
<fig id="F4" position="float">
<label>Figure 4</label>
<caption><p>Total and partial average use consensus (UC), according to biogeographic origin of the firewood species in the different categories of landscape (domestic, semi-domestic and low human intervention): Key: &#x025A0; UC of native plants; &#x025A0; UC of exotic plants; &#x025A0; Total UC. A: No significant differences to use consensus between different categories of landscape (<italic>p</italic> &#x0003E; 0.05). a: No significant differences to use consensus according to biogeographic origin of the firewood species in each different categories of landscape (<italic>p</italic> &#x0003E; 0.05).</p></caption>
<graphic xlink:href="fevo-05-00111-g0004.tif"/>
</fig>
<p>Results relating to biogeographic origin also went against our hypothesis, as no differences were found in the use of the different landscapes for the gathering of native (Kruskal-Wallis test &#x0003D; 0.160, Figure <xref ref-type="fig" rid="F4">4</xref>) or exotic firewood plants (Kruskall-Wallis test, <italic>p</italic> &#x0003D; 0.399, Figure <xref ref-type="fig" rid="F4">4</xref>). Nevertheless, the average value for UC of the native species is higher in the semi-domestic than in the domestic landscape, and the average UC value for the exotic species is higher in the semi-domestic and domestic areas than in those of low human intervention.</p>
</sec>
</sec>
<sec>
<title>Versatility of use of firewood species</title>
<p>Of all informants&#x00027; cites, 71.2% referred to plants which were used only for firewood (cooking and heating) (Table <xref ref-type="table" rid="T2">2</xref>). The remaining cites made reference to firewood species which were also used for other purposes, from two to three different uses (i.e., construction materials, fodder, dye, medicine, food). The species of highest use versatility are exotic: <italic>P</italic>. <italic>alba, Salix</italic> sp, <italic>Prunus cerasus</italic>, and <italic>Malus domestica</italic>.</p>
<table-wrap position="float" id="T2">
<label>Table 2</label>
<caption><p>Summary of cases for variables of multinomial logistic model representing the firewood species gathered by the Mapuche communities of Costa del Lep&#x000E1; and Gualjaina.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>Variables</bold></th>
<th valign="top" align="left"><bold>Categories</bold></th>
<th valign="top" align="center"><bold><italic>N</italic></bold></th>
<th valign="top" align="center"><bold>Percentage of cites</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left" colspan="4" style="background-color:#bbbdc0"><bold>DEPENDENT VARIABLE</bold></td>
</tr>
<tr>
<td valign="top" align="left">Landscape unit</td>
<td valign="top" align="left">1. Low human intervention</td>
<td valign="top" align="center">84</td>
<td valign="top" align="center">47.5</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">2. Semi-domestic</td>
<td valign="top" align="center">59</td>
<td valign="top" align="center">33.3</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">3. Domestic</td>
<td valign="top" align="center">34</td>
<td valign="top" align="center">19.2</td>
</tr>
<tr>
<td valign="top" align="left" colspan="4" style="background-color:#bbbdc0"><bold>INDEPENDENT VARIABLES</bold></td>
</tr>
<tr>
<td valign="top" align="left">Biogeographic origin</td>
<td valign="top" align="left">1. Native</td>
<td valign="top" align="center">131</td>
<td valign="top" align="center">74.0</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">2. Exotic</td>
<td valign="top" align="center">46</td>
<td valign="top" align="center">26.0</td>
</tr>
<tr>
<td valign="top" align="left">Use versatility</td>
<td valign="top" align="left">1. Exclusively fuel</td>
<td valign="top" align="center">126</td>
<td valign="top" align="center">71.2</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">2. Fuel plus other uses</td>
<td valign="top" align="center">51</td>
<td valign="top" align="center">28.8</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><italic>Frequency represents the total number of plant cites for each sub-category</italic>.</p>
</table-wrap-foot>
</table-wrap>
<sec>
<title>Versatility of use of firewood plants according to the level of landscape domestication and biogeographic origin</title>
<p>The average use versatility of the firewood species showed no variation between the different landscapes in terms of their level of domestication (Kruskall-Wallis test, <italic>p</italic> &#x0003D; 0.19, Figure <xref ref-type="fig" rid="F5">5</xref>). Neither did they show significant differences between types of landscape in terms of biogeographic origin (Kruskall-Wallis test <italic>p</italic> &#x0003E; 0.05, Figure <xref ref-type="fig" rid="F5">5</xref>). In the domestic area, 60% of the species (6 species) are used for multiple purposes, while 4 are used only for fuel (40% of the total), although these differences are non-significant (Binomial test, <italic>p</italic> &#x0003D; 0.75). In the semi-domestic areas, in contrast, fewer of the firewood plants are used for multiple purposes (18%, 3 species) than those used for fuel alone (82%, 14 species) (Binomial test, <italic>p</italic> &#x0003D; 0.013). The landscape with least human intervention follows the same pattern.</p>
<fig id="F5" position="float">
<label>Figure 5</label>
<caption><p>Average use versatility (UV) of species according to biogeographic origin, and total value for the different landscape categories (domestic, semi-domestic and low human intervention): Key: &#x025A0; UV of native plants; &#x025A0; UV of exotic plants; &#x025A0; Total UV. A: No significant differences to versatility between different categories of landscape (<italic>p</italic> &#x0003E; 0.05). a: No significant differences to versatility according to biogeographic origin of the firewood species in each different categories of landscape (<italic>p</italic> &#x0003E; 0.05).</p></caption>
<graphic xlink:href="fevo-05-00111-g0005.tif"/>
</fig>
<p>In the domestic areas, the UC of multi-use combustible species (17.2% &#x000B1; 7.50) was higher than the species used exclusively for fuel (3.4% &#x000B1; 0), although these differences were not significant (Mann Whitney <italic>U</italic>-test, <italic>p</italic> &#x0003D; 0.11, Figure <xref ref-type="fig" rid="F6">6</xref>). The multi-use combustible species with highest UC was <italic>P. alba</italic> (48.3%). The semi-domestic landscape followed a similar pattern, since the multi-use combustible species (19.5% &#x000B1; 12.8) presented higher UC than the fuel-only species (8.9% &#x000B1; 1.2), but without significant differences (Mann Whitney <italic>U</italic>-test, <italic>p</italic> &#x0003D; 0.59, Figure <xref ref-type="fig" rid="F6">6</xref>). <italic>Salix</italic> sp., a multi-use species, was the most frequently cited (44.8%).</p>
<fig id="F6" position="float">
<label>Figure 6</label>
<caption><p>Comparison of use consensus according to versatility of use of firewood species for the different landscape categories (domestic, semi-domestic and low human intervention): Key: &#x025A0; Fuel-only species; &#x025A0; Multiple use species. a: No significant differences according to versatility of use of firewood species for the different landscape categories (<italic>p</italic> &#x0003E; 0.05).</p></caption>
<graphic xlink:href="fevo-05-00111-g0006.tif"/>
</fig>
<p>In contrast, in the low intervention landscape the UC of fuel-only species (9.6% &#x000B1; 2.05) was higher than the multi-use species (3.4% &#x000B1;0), although not significant (Mann Whitney <italic>U</italic>-test, <italic>p</italic> &#x0003D; 0.15, Figure <xref ref-type="fig" rid="F6">6</xref>). <italic>Schinus johnstonii</italic> (31%) and <italic>N</italic>. <italic>axillaris</italic> (17.2%), fuel-only species, were the most frequently cited plants.</p>
</sec>
</sec>
<sec>
<title>Continuity of use of firewood species</title>
<p>Of all the combustible species registered, only three correspond to plants currently out of use (10.7% of the total); inhabitants reported using them during their infancy. According to informants, the native shrub species <italic>Prosopis denudans</italic> var. <italic>patagonica, Retanilla patagonica</italic>, and <italic>Atriplex lampa</italic> are not in current use, a fact associated with their lack of regeneration and lack of access to the plants.</p>
<p>Despite the limited nature of their firewood resources, Mapuche communities allow neighbors to have free access to the semi-domestic and low anthropic intervention landscapes for firewood gathering, without establishing previous agreements within the communities to regulate this use. However, some sectors in the region have been appropriated by the previously mentioned livestock companies, which forbid the extraction of firewood plants and are drastically altering provision strategies.</p>
<p>The remaining species have a history of continuous use (11 species; 39.3%), amongst which <italic>S. johnstonii, N. axillaris</italic> and <italic>Corynabutilon bicolor</italic> are worthy of special note, being found mainly in the low anthropic intervention environments; either they have been incorporated gradually (16 species in current use, 50% del total) due to their environmental (i.e., cultivated species such as <italic>P. alba, P. cerasus, M. domestica</italic>, and <italic>Ulmus minor</italic>), and/or commercial availability, such as <italic>Pinus</italic> ssp. and <italic>N. antarctica</italic>. The firewood plants which have been used for a long time have a higher UC (31.2% &#x000B1; 6.2) than both those recently incorporated (12.5% &#x000B1; 5.6) and those which are no longer used (7.3% &#x000B1; 2.1) (K-Wallis test, <italic>p</italic> &#x0003D; 0.003).</p>
</sec>
<sec>
<title>Differential use of the landscape according to biogeographic origin and use versatility of combustible species</title>
<p>Descriptions of the variables analyzed and the distribution of all cases are detailed in Table <xref ref-type="table" rid="T2">2</xref>. The model to explain variation in the proportion of plants with different biogeographic origins and use versatility in the landscapes analyzed together was found to be significant (&#x003C7;<sup>2</sup>: 110, <italic>df</italic> &#x0003D; 4, <italic>p</italic> &#x0003C; 0.05). Other models that considered continuity of use and life form did not give significant results, so these variables were excluded. By means of this multinomial analysis which evaluates the weight of variables as a function of the other variables, it was found that the biogeographic origin of the firewood plants varied for the different classes of landscape (&#x003C7;<sup>2</sup>: 20.6, <italic>df</italic> &#x0003D; 2, <italic>p</italic> &#x0003C; 0.05). This result contributes more information than the univariate analysis (Figure <xref ref-type="fig" rid="F4">4</xref>). In the landscape with low human intervention, the probability of native plants use is 100 times greater in the domestic landscape (<italic>p</italic> &#x0003C; 0.05, Table <xref ref-type="table" rid="T3">3</xref>). Furthermore, the semi-domestic landscape showed no variation in biogeographic origin in relation to the domestic landscape (<italic>p</italic> &#x0003D; 0.07, Table <xref ref-type="table" rid="T3">3</xref>). In contrast, for exotic species the patterns are reversed; the domestic areas have 100 times as many exotic plants as those with low human intervention. The use versatility of firewood plants did not vary with the different levels of landscape domestication (&#x003C7;<sup>2</sup>: 0.8, <italic>df</italic> &#x0003D; 2, <italic>p</italic> &#x0003D; 0.66). As was found previously with univariated analysis, the availability of combustible species with greater use versatility does not seem to be associated with domestication of the landscape.</p>
<table-wrap position="float" id="T3">
<label>Table 3</label>
<caption><p>Parameters estimated from the multinomial regression.</p></caption>
<table frame="hsides" rules="groups">
<thead><tr>
<th valign="top" align="left"><bold>Landscape category<xref ref-type="table-fn" rid="TN2"><sup>a</sup></xref></bold></th>
<th/>
<th valign="top" align="center"><bold>B</bold></th>
<th valign="top" align="center"><bold>Std. error</bold></th>
<th valign="top" align="center"><bold>Wald</bold></th>
<th valign="top" align="center"><bold>df</bold></th>
<th valign="top" align="center"><bold>Sig</bold>.</th>
<th valign="top" align="center"><bold>Exp(B)</bold></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Low human intervention</td>
<td valign="top" align="left">Interception</td>
<td valign="top" align="center">&#x02212;18.693</td>
<td valign="top" align="center">1.344</td>
<td valign="top" align="center">193.517</td>
<td valign="top" align="center">1</td>
<td valign="top" align="center">0.000</td>
<td/>
</tr>
<tr>
<td/>
<td valign="top" align="left" colspan="7"><bold>Origin</bold></td>
</tr>
<tr>
<td/>
<td valign="top" align="left">Native</td>
<td valign="top" align="center">20.543</td>
<td valign="top" align="center">0.000</td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">1</td>
<td valign="top" align="center">0.000<xref ref-type="table-fn" rid="TN4"><sup>&#x0002A;</sup></xref></td>
<td valign="top" align="center">835176490.0</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">Exotic</td>
<td valign="top" align="center">0<xref ref-type="table-fn" rid="TN3"><sup>b</sup></xref></td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">0</td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">.</td>
</tr>
<tr>
<td/>
<td valign="top" align="left" colspan="7"><bold>Versatility of use</bold></td>
</tr>
<tr>
<td/>
<td valign="top" align="left">Fuel only</td>
<td valign="top" align="center">1.283</td>
<td valign="top" align="center">1.384</td>
<td valign="top" align="center">0.859</td>
<td valign="top" align="center">1</td>
<td valign="top" align="center">0.354</td>
<td valign="top" align="center">3.608</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">Fuel plus other uses</td>
<td valign="top" align="center">0<xref ref-type="table-fn" rid="TN3"><sup>b</sup></xref></td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">0</td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">.</td>
</tr>
<tr style="border-top: thin solid #000000;">
<td valign="top" align="left">Semi-domestic</td>
<td valign="top" align="left">Interception</td>
<td valign="top" align="center">&#x02212;0.646</td>
<td valign="top" align="center">0.312</td>
<td valign="top" align="center">4.302</td>
<td valign="top" align="center">1</td>
<td valign="top" align="center">0.038</td>
<td/>
</tr>
<tr>
<td/>
<td valign="top" align="left" colspan="7"><bold>Origin</bold></td>
</tr>
<tr>
<td/>
<td valign="top" align="left">Native</td>
<td valign="top" align="center">2.326</td>
<td valign="top" align="center">1,276</td>
<td valign="top" align="center">3.320</td>
<td valign="top" align="center">1</td>
<td valign="top" align="center">0.068</td>
<td valign="top" align="center">10.234</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">Exotic</td>
<td valign="top" align="center">0<xref ref-type="table-fn" rid="TN3"><sup>b</sup></xref></td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">0</td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">.</td>
</tr>
<tr>
<td/>
<td valign="top" align="left" colspan="7"><bold>Versatility of use</bold></td>
</tr>
<tr>
<td/>
<td valign="top" align="left">Fuel only</td>
<td valign="top" align="center">0.760</td>
<td valign="top" align="center">1.294</td>
<td valign="top" align="center">0.345</td>
<td valign="top" align="center">1</td>
<td valign="top" align="center">0.557</td>
<td valign="top" align="center">2.139</td>
</tr>
<tr>
<td/>
<td valign="top" align="left">Fuel plus other uses</td>
<td valign="top" align="center">0<xref ref-type="table-fn" rid="TN3"><sup>b</sup></xref></td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">0</td>
<td valign="top" align="center">.</td>
<td valign="top" align="center">.</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><italic>B, Beta; Wald is the chi-square that tests the null hypothesis, df, degrees of freedom; Sig., level of significance and Exp (B) &#x0003D; Odds ratios calculated by exponentiation of the coefficients (the probability that an event will happen in relation to the probability it will not)</italic>.</p>
<fn id="TN2">
<label>a</label>
<p><italic>The reference category is: Domestic landscape</italic>.</p></fn>
<fn id="TN3">
<label>b</label>
<p><italic>This parameter is established as zero since it is redundant</italic>.</p></fn>
<fn id="TN4">
<label>&#x0002A;</label>
<p><italic>This symbol indicates significant differences</italic>.</p></fn>
</table-wrap-foot>
</table-wrap>
</sec>
</sec>
<sec sec-type="discussion" id="s4">
<title>Discussion</title>
<p>Our results show that the landscapes with a lower level of domestication are not the most intensively used, not in terms of number of species, use intensity or species with higher use versatility. For the two communities living on the Chubut steppe, gathering patterns of firewood plants depend entirely on landscapes with different levels of domestication, which are used in an articulated way. This gathering pattern is dynamic and possibly evolves with the changes that come about in the landscape and other factors such as livestock breeding. All these environments created according to the needs of locals are used in a complementary way, possibly indicating &#x0201C;prudent&#x0201D; (Shaanker et al., <xref ref-type="bibr" rid="B68">2003</xref>) and diversified use of these resources, so that the impact of gathering is distributed across the entire environmental gradient (Cardoso et al., <xref ref-type="bibr" rid="B20">2017</xref>). This reflects an integrated concept of the landscape, as has been widely documented for different traditional peoples in Argentina (Crivos et al., <xref ref-type="bibr" rid="B30">2004</xref>; Pirondo and Keller, <xref ref-type="bibr" rid="B62">2014</xref>). In other words, the landscape units present spatial continuity in response to ecological gradient, type of management and the multiple interconnections generated by the inhabitants and their domestic animals, all of which is accompanied by global exploitation (Capparelli et al., <xref ref-type="bibr" rid="B15">2011</xref>; Molares and Ladio, <xref ref-type="bibr" rid="B58">2012</xref>, <xref ref-type="bibr" rid="B59">2014</xref>).</p>
<p>The communities of Costa del Lep&#x000E1; and Gualjaina obtain in total 28 different firewood species, a richness similar to that registered by Cardoso et al. (<xref ref-type="bibr" rid="B18">2012</xref>), who recorded 27 species in other rural zones on the Patagonian steppe. This richness is the result of diverse use of the landscape and the integration of new supply strategies, such as purchase and social welfare plans (Cardoso et al., <xref ref-type="bibr" rid="B19">2013</xref>). The species are shared little between environments, considering the intentional addition of exotic and new species in the most domesticated landscape, mainly for firewood purposes. However, the low diversity of species in these environments (10 species) coincides with domestication patterns that tend toward a reduction in the number of species, monoculture and specialization of species (Amico, <xref ref-type="bibr" rid="B4">2002</xref>). The three types of environment analyzed showed no significant differences in the proportions of native and exotic species gathered, indicating that gathering pressure is shared between the different landscapes. Nevertheless, the multinomial analysis showed that the probability of collecting native plants is 100 times higher in environments with low domestication, while the reverse is true for exotic species. The inhabitants have incorporated a high proportion of exotic species through cultivation, in addition to those species which have begun to grow in the wild. This could be favored by the decreasing availability of native resources and the strong influence of external government organizations which provide technical support that promotes the incorporation of exotic resources (Eyssartier et al., <xref ref-type="bibr" rid="B35">2013</xref>). The use of exotic species in domestic landscapes in Patagonia and other regions of the world has been highlighted by several authors to be a local solution to various needs, since in general they are easily available, fast growing, and more tolerant than native species (Eyssartier et al., <xref ref-type="bibr" rid="B34">2009</xref>; Dos Santos et al., <xref ref-type="bibr" rid="B32">2010</xref>; Richeri et al., <xref ref-type="bibr" rid="B65">2013</xref>; Rovere et al., <xref ref-type="bibr" rid="B66">2013</xref>), in addition to complementing native species, covering new needs, and diversifying the offer of useful plants (Albuquerque, <xref ref-type="bibr" rid="B1">2006</xref>; Medeiros, <xref ref-type="bibr" rid="B54">2013</xref>; Ladio and Albuquerque, <xref ref-type="bibr" rid="B45">2014</xref>).</p>
<p>The semi-domesticated landscape, which includes mainly river valleys, with an intermediate level of human intervention, was also a significant site for the gathering of firewood. In these environments the species richness of native plants gathered is higher than that of exotics, although the latter are the most used. The more frequent use of the exotic species may be associated with their abundance, accessibility and quality, as observed in other studies (Albuquerque et al., <xref ref-type="bibr" rid="B2">2009</xref>; Cardoso et al., <xref ref-type="bibr" rid="B18">2012</xref>). One notable example of this is <italic>Salix</italic> sp., an exotic species of rapid growth that quickly colonizes and becomes established on most Patagonian riverbanks, in many cases displacing the native species <italic>S. humboltiana</italic>, and competing successfully for resources and suitable regeneration sites (Bozzi et al., <xref ref-type="bibr" rid="B13">2014</xref>).</p>
<p>In contrast, the landscapes where there had been relatively little anthropic intervention presented the greatest number of cites for native firewood plants (100 times more than the most domesticated environment). Previous investigations carried out in similar environments in Patagonia have highlighted the important use of native species for firewood, compared to exotics (Cardoso et al., <xref ref-type="bibr" rid="B18">2012</xref>). <italic>Schinus johnstonii</italic> is the most frequently gathered resource in this landscape. The cultural importance of this species over time has been documented in archaeobotanical studies and in recent work in the region, highlighting this species&#x00027; characteristics of high calorific value and long-lasting embers (Ancibor and P&#x000E9;rez de Micou, <xref ref-type="bibr" rid="B5">1995</xref>; Cardoso et al., <xref ref-type="bibr" rid="B19">2013</xref>; Morales et al., <xref ref-type="bibr" rid="B60">2017</xref>).</p>
<p>The results also indicate that there is no variation in pattern of use of the landscape in terms of use versatility, and that in general terms the combustible plants are not very versatile, possibly due to their fuel uses (heating and cooking) being prioritized in the interview. Even so, it must be mentioned that the firewood plants, as well as providing energy, are a source of animal fodder, are used in making shelters for the animals and in construction, as also found by Cardoso et al. (<xref ref-type="bibr" rid="B18">2012</xref>) and Morales et al. (<xref ref-type="bibr" rid="B60">2017</xref>). These authors highlight the fact that the introduction of rapidly growing exotic firewood plants in peri-domestic areas increases the richness of uses of the flora, revealing mechanisms that improve inhabitants&#x00027; self-sufficiency.</p>
<p>It is interesting to note the dynamics of use of the different landscape areas over time. According to informants, during their infancy the semi-domestic and low anthropic intervention environments were of more importance for plant gathering than they are now, given their higher offer of species with high calorific value. At the present time, the extraction of firewood is affected by the work of large livestock companies, as well as the increasing problem of desertification due to overgrazing, amongst other factors, which cause damage to the soil and plant cover. These phenomena gradually configure a new landscape, thus generating the need for new strategies to obtain supplies (Marconetto, <xref ref-type="bibr" rid="B53">2006</xref>).</p>
<p>Analysis of the interviews reveals that historically, the purchase of firewood species was infrequent in the studied communities, as was the use of gas. It has been recorded that half the population now buys firewood plants, mainly <italic>N. antarctica</italic>, which comes from the Sub-Antarctic Forest, and is one of the most commonly used and most commercially exploited species (Arre et al., <xref ref-type="bibr" rid="B6">2015</xref>). The current tendency to purchase firewood, as a provision strategy, has also been observed in other rural communities (Ramos et al., <xref ref-type="bibr" rid="B64">2008</xref>; Cardoso et al., <xref ref-type="bibr" rid="B18">2012</xref>); in this way the factor of uncertainty in the availability of these subsistence resources, as conceptualized by Blancas et al. (<xref ref-type="bibr" rid="B11">2014</xref>), is decreased.</p>
<p>Together with the preferential use of species adapted to the disturbances typical of these environments (e.g., fires, overgrazing) (Morales et al., <xref ref-type="bibr" rid="B60">2017</xref>), this suggests an articulated, dynamic system in which processes of climate and socio-political change (decrease in precipitation, mineral extractivism, etc.), flora and populations all coevolve. Thus, complementary use of the landscape, selection of species that grow quickly after harvesting and innovation in supply strategies (purchase), understood as local responses to the problem of change (Ladio, <xref ref-type="bibr" rid="B44">2017</xref>), promote faster recuperation of the landscape and woody species, decreasing uncertainty and increasing biocultural resilience (Ladio, <xref ref-type="bibr" rid="B44">2017</xref>; Morales et al., <xref ref-type="bibr" rid="B60">2017</xref>). For example, some informants revealed that since many people have started buying firewood, regeneration of native plants such as <italic>Retanilla patagonica</italic> has been observed. This moment in the collective memory of the studied populations marks the beginning of an indirect process of promotion of the availability of this species, so that it can be used in the future; this is, therefore, management that will promote domestication of the environment.</p>
</sec>
<sec sec-type="conclusions" id="s5">
<title>Conclusions</title>
<p>Firewood gathering has always been stigmatized and associated with practices considered as destructive, and carried out by poor communities. In our case study visibilization of the firewood gathering practice from the perspective of landscape domestication allows us to reveal more complex, integral processes. Although native plants are much used and obtained from environments with a low level of domestication, inhabitants do not seem to concentrate their efforts on those environments alone. Medium and high domestication level landscapes contribute exotic (and native) plants which play a substantial role, alleviating use pressure on native species, and while this cannot prevent over exploitation, it does minimize it. The continuity of use of wood for combustible purposes is also favored, guaranteeing a supply of this resource, fundamental for subsistence, and an important component of the locals&#x00027; lifestyle. Complementary use of the landscape is the underlying logic, but the incipient domestication of species present in the totally domesticated environments is also an interesting aspect that should be studied in more depth. The growth of these plants (10 species) is being encouraged with irrigation, thermal and wind protection, pruning, the adding of organic material from home composting, etc., which generates greater production of firewood and reduces impact in terms of extraction of native species.</p>
<p>In the arid region of Patagonia significant effects are expected in the coming years, in association with global climate change. These changes will no doubt affect the communities whose subsistence depends on their close bond with the landscape and its resources (Rabassa, <xref ref-type="bibr" rid="B63">2010</xref>). Within this scenario it is essential to review government strategies and conservation plans, which are always top-down. The inclusion of bottom-up perspectives on the subject of firewood is necessary in order to find solutions that take local management and cosmologies into account in an inclusive way (Ladio, <xref ref-type="bibr" rid="B44">2017</xref>). Our empirical information reveals that the inhabitants of Patagonia are creating new environments with richness and versatility of use, and seeking new alternatives in the face of firewood scarcity, through landscape domestication.</p>
</sec>
<sec id="s6">
<title>Author contributions</title>
<p>AL and SM conceived of the study, designed the questionnaires, participated in data analysis and performed statistical analysis. DM carried out questionnaires among the Mapuche communities, analyzed the tales, performed statistical analysis and drafted the manuscript. The three authors read and approved the final manuscript.</p>
<sec>
<title>Conflict of interest statement</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
</sec>
</body>
<back>
<ack><p>Our thanks are due to the inhabitants of the Costa del Lep&#x000E1; and Gualjaina communities for their friendly disposition, generous help, and for sharing their knowledge and experience. We are also grateful to the two reviewers whose suggestions helped improve this work substantially. This research was supported by PIP 0466 of CONICET.</p>
</ack>
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