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The need for multidisciplinary conservation: a case study of Ceratozamia (Zamiaceae, Cycadales) in eastern Mexico

Published online by Cambridge University Press:  24 March 2021

Lilí Martínez-Domínguez
Affiliation:
Laboratorio de Taxonomía Integrativa, Instituto de Investigaciones Biológicas, Universidad Veracruzana, Xalapa, 91190, Veracruz, Mexico
Fernando Nicolalde-Morejón*
Affiliation:
Laboratorio de Taxonomía Integrativa, Instituto de Investigaciones Biológicas, Universidad Veracruzana, Xalapa, 91190, Veracruz, Mexico
Dennis Wm. Stevenson
Affiliation:
The New York Botanical Garden, New York, USA
Quiyari J. Santiago-Jiménez
Affiliation:
Facultad de Biología, Universidad Veracruzana, Xalapa, Veracruz, Mexico
Octavio Rojas-Soto
Affiliation:
Laboratorio de Bioclimatología, Red de Biología Evolutiva, Instituto de Ecología, Xalapa, Veracruz, Mexico
Francisco Vergara-Silva
Affiliation:
Laboratorio de Sistemática Molecular, Jardín Botánico, Instituto de Biología, Universidad Nacional Autónoma de México, Coyoacán, Mexico
*
(Corresponding author) E-mail enicolalde@uv.mx

Abstract

As an evolutionary lineage cycads are rare, and the extinction risk is high for many species. The genus Ceratozamia, one of the most diverse in Mexico, is experiencing drastic reductions of its habitat. Ceratozamia is widely distributed along the Sierra Madre Oriental, a complex mountain range, in a region characterized by high ecological and cultural diversity. Since 1990, various conservation and management strategies have been applied to this taxon in Mexico but evidence for the effectiveness of these measures is lacking. Ceratozamia in the Mexican Sierra Madre Oriental is highly diverse and endemic, offering a model for analysing geographical distribution patterns with ecological niche modelling. It also presents an opportunity for assessing the success of conservation and management strategies that have been implemented in this area. Here, we examined three aspects that are considered fundamental for the development and evaluation of conservation strategies: (1) taxonomy, (2) ecology and (3) sociocultural anthropology. Our findings suggest a pessimistic outlook for the long-term survival of Ceratozamia species in their natural environment, indicating the need to review the current IUCN Cycad Action Plan for the genus. To improve the protection of Ceratozamia and other taxonomic and/or ecological assemblages, we encourage a multidisciplinary approach, with increased collaboration between natural and social scientists.

Type
Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press on behalf of Fauna & Flora International

Introduction

The genus Ceratozamia (Zamiaceae: Cycadales) is widely distributed and highly diverse in Mexico, with 30 species occurring in the country (Calonje et al., Reference Calonje, Stevenson and Osborne, R.2019). Nearly 40% of Ceratozamia species are endemic to the Sierra Madre Oriental, a complex mountain range that harbours the greatest diversity of species belonging to this genus. Given the threatened status of Ceratozamia (the genus is listed on CITES Appendix I, and several species are categorized as threatened on the IUCN Red List; CITES, 2019), there is an urgent need to develop conservation strategies, but this is hampered by a paucity of information on cycad distribution.

Cycads grow slowly, can live for several hundred years and struggle to survive in disturbed habitats, making them important indicators of habitats in good conservation status (Norstog & Nicholls, Reference Norstog and Nicholls1997). Assessing cycad distribution could thus contribute to the mapping of priority areas for ecosystem conservation in Mexico. The most threatened vegetation types in Mexico are oak, pine–oak and cloud forests, which occur widely in the Sierra Madre Oriental and are characteristic habitats for most species of Ceratozamia (Contreras-Medina, Reference Contreras-Medina, Luna, Morrone and Espinosa-Organista2004).

The Cycad Action Plan (Donaldson, Reference Donaldson2003) is an international initiative of the IUCN Cycad Specialist Group focusing on sustainable use and ex situ conservation. These approaches have led to a number of international initiatives (Graham et al., Reference Graham, Bonta and Ulloa2011; Griffith et al., Reference Griffith, Calonje, Meerow, Tut, Kramer and Hird2015), with the main focus being on the cultivation of cycads in nurseries. This is also the case in Mexico, where the most frequently proposed conservation action has been the establishment of nurseries to support sustainable management of cycads, which are often planted for ornamental purposes (Vovides & Iglesias, Reference Vovides and Iglesias1994; Vovides et al., Reference Vovides, Pérez-Farrera, Vázquez-Torres, Schippmann, Maunder, Clubbe, Hankamer and Groves2002).

The conservation of Ceratozamia is hampered by poor taxonomic curation of botanical specimens deposited in Mexican herbaria and elsewhere, lack of taxonomic revisions and limited knowledge of the taxonomic relationships of species within the genus. To study the biology of species, delimit species distributions and assess extinction risk, correct identification and naming of species is important (Wheeler et al., Reference Wheeler, Knapp, Stevenson, Stevenson, Blum and Boom2012; Mota-Vargas & Rojas-Soto, Reference Mota-Vargas and Rojas-Soto2016), but the distribution of the various species of Ceratozamia in the Sierra Madre Oriental remains poorly known. Some Ceratozamia species occur within designated protected areas, but how many or which ones is unknown.

Ecological niche modelling predicts the distribution of species using spatial analysis of environmental variables (Holt, Reference Holt2009). It is a valuable tool for the development and evaluation of conservation strategies (Peterson et al., Reference Peterson, Sánchez-Cordero, Martínez-Meyer and Navarro-Sigüenza2006) and has been shown to be effective in studies of the distribution of many taxa (Mota-Vargas & Rojas-Soto, Reference Mota-Vargas and Rojas-Soto2012; Peterson & Soberón, Reference Peterson and Soberón2012), but has rarely been used in analyses of the distribution of cycads.

Evidence of the effectiveness of current conservation actions for Mexican Ceratozamia species is lacking. Outcomes of ongoing conservation programmes, which involve participation of local communities in the propagation and care of nursery plants, have not been evaluated (Vovides et al., Reference Vovides, Pérez-Farrera and Iglesias2010), and potential conceptual and methodological shortcomings that could restrict their success have not been considered (Bottrill & Pressey, Reference Bottrill and Pressey2012). In addition, there is a disconnect between conservation policies and management strategies recommended by biologists and the needs and activities of local communities. This calls for collaborative, multidisciplinary approaches, with the aim to implement conservation strategies in partnership between local communities and conservation biologists/managers (Orlove & Brush, Reference Orlove and Brush1996).

Here, we evaluate the conservation and management strategies for Ceratozamia in the Sierra Madre Oriental, using multidisciplinary methods from both natural and social sciences (Halme et al., Reference Halme, Kuusela and Juslén2015; Bennett, Reference Bennett2016). Specifically, we examine the taxonomy and biogeographical characteristics of the genus, and local perceptions of, and attitudes towards, existing conservation programmes. We also discuss prospects for additional multidisciplinary approaches for the conservation of cycads.

Study area

The Sierra Madre Oriental is a mountain range that emerges from the coastal plain of the Gulf of Mexico towards the central high plateau of Mexico. It is 800 km long and 80–100 km wide (Eguiluz de Antuñano et al., Reference Eguiluz de Antuñano, Aranda-García and Marrett2000). Ceratozamia species occur at an altitude of 600–2,000 m on karstic rocks. People living in this area are ethnically diverse and practice subsistence- and market-oriented production (Toledo et al., Reference Toledo, Ortiz-Espejel, Cortés, Moguel and Ordoñez2003).

Methods

Species data

We obtained occurrence records for Ceratozamia by reviewing the 323 specimens available in the following herbaria: CHAPA, CIB, ENCB, FCME, FTG, GH, HEM, IEB, K, LE, LSU, MB, MICH, MEXU, MO, NY, P, SERO, SLPM, U, UAT, US, XAL, and XALU (acronyms according to Index Herbariorum; Thiers, Reference Thiers2019). This review was based on the taxonomic concepts of species proposed by Nicolalde-Morejón et al. (Reference Nicolalde-Morejón, González-Astorga, Vergara-Silva, Stevenson, Rojas-Soto and Medina-Villarreal2014) and Martínez-Domínguez et al. (Reference Martínez-Domínguez, Nicolalde-Morejón, Vergara-Silva and Stevenson2018). We also included information collected in the field during 2014–2017. We conducted fieldwork on 41 Ceratozamia populations throughout the Mexican Sierra Madre Oriental, to corroborate existing records and/or obtain new localities for species. Because of the clustered distribution of species, we used preliminary information on distribution and ecological requirements to locate Ceratozamia populations. In 22 localities we interviewed local people, showing them photographs and describing the morphological characters representative of the genus, and asking about potential sites in the vicinity that may have suitable habitat for cycads, such as karstic rocks. We recorded the geographical coordinates of each site where we located cycad plants and compiled this information in a database in ArcMap 10.2 (Esri, Redlands, USA). Records without precise locality data, or with coordinates that could not be corroborated during fieldwork, were omitted. To examine the distribution of Ceratozamia in the Sierra Madre Oriental, we superimposed the points of occurrence on the biogeographical province proposed by Paniagua & Morrone (Reference Paniagua and Morrone2009).

Environmental layers, ecological niche modelling and distribution

We used interpolated climatic layers of 19 bioclimatic variables from WorldClim (Hijmans et al., Reference Hijmans, Cameron, Parra, Jones and Jarvis2005) at a spatial resolution of 30" (c. 1 km2 cell size) to characterize ecological niches. We reduced dimensionality and collinearity between the bioclimatic layers by applying principal component analysis (PCA) with the function PCARaster in the R 3.3.1 package ENMGadgets (Barve & Barve, Reference Barve and Barve2013; R Development Core Team, 2018). We retained the first six components for modelling because they explained c. 95% of the overall variance in environments for all species. Niche modelling was performed with Maxent (Phillips et al., Reference Phillips, Anderson and Schapired2006) because of its high predictive capability with presence-only data (Elith et al., Reference Elith, Kearney and Phillips2010), and the dismo package (Hijmans et al., Reference Hijmans, Phillips, Leathwick and Elith2011) in R. Because the seeds of cycads are dispersed mainly by gravity (rarely by rodents, and then only over short distances), watersheds could be barriers to the dispersion of the species. We calibrated models within the accessible area (i.e. the area where the species could occur considering dispersion barriers and the historic conditions in the region) for each species (Barve et al., Reference Barve, Barve, Jiménez-Valverde, Lira-Noriega, Mahera and Peterson2011). We used polygons representing the watershed system of Mexico, and selected those polygons where at least one record was present. Because of the small number of records, we used 80% of occurrences for calibration. Models included five bootstrap-type replicas, and we selected those with the highest value for the area under the receiver operating characteristic curve (AUC). We transformed the predictions obtained into a binary map (0 = absence, 1 = presence), including the total number of records in all cases corresponding to the lowest presence threshold (i.e. the minimum training presence of Maxent). We validated model predictions for species with < 20 presence records through jackknife tests (Pearson et al., Reference Pearson, Raxworthy, Nakamura and Peterson2007); for species with ≥ 20 records, analyses were conducted with PartialROC (Barve, Reference Barve2008; Peterson et al., Reference Peterson, Papes and Soberón2008; Supplementary Table 1).

Evaluation of current conservation and management strategies

The binary models were summed using the Algebra map tool in ArcMap, and then reclassified to produce a richness accumulation map. Although this method could potentially overestimate species richness in some areas, we believe it is suitable here because it did not predict areas that would not be suitable for Ceratozamia (e.g. Calabrese et al., Reference Calabrese, Certain, Kraan and Dormann2014; D'Amen et al., Reference D'Amen, Dubuis, Fernandes, Pottier, Pellissier and Guisan2015a,Reference D'Amen, Pradervand and Guisanb). To visualize areas potentially affected by anthropogenic land-use changes, we clipped species richness maps using the most recent series of data on land use and vegetation coverage provided by the Mexican Instituto Nacional de Geografía y Estadística (INEGI, 2013). To assess the role of protected areas programmes, we evaluated species richness in areas of four protection categories: State, Municipal, Common Land and Private Natural Protected Areas, following the Mexican Comisión Nacional para el Uso y Conservación de la Biodiversidad (CONABIO, 2015) and the Federal Natural Protected Areas 2014 of the Mexican Comisión Nacional de Áreas Naturales Protegidas (CONANP, 2014). We also considered Priority Terrestrial Regions (CONABIO, 2004) and main regions and subregions of the cloud forest in Mexico (CONABIO, 2008). In addition, we overlaid species richness concentrations upon a cultural map (Boege, Reference Boege2008), to evaluate the geographical correspondence of Ceratozamia diversity with the distribution of ethnic groups.

To evaluate ex situ conservation efforts, we consulted with the curators or directors of the major botanical gardens in Mexico, either by visiting the collections or via e-mail. To assesses the contribution of botanical gardens to Ceratozamia conservation, we confirmed the species identities of live specimens kept in botanical garden collections, using the taxonomic key by Martínez-Domínguez et al. (Reference Martínez-Domínguez, Nicolalde-Morejón, Vergara-Silva and Stevenson2018). In addition, we identified two nurseries for Ceratozamia in the Sierra Madre Oriental (Vovides et al., Reference Vovides, Pérez-Farrera and Iglesias2010), in the municipality of Coacoatzintla (Veracruz State): Tachinola and Dos Cerros. Both nurseries grew C. tenuis.

To examine local perceptions of the nurseries, we interviewed people with varying degrees of involvement in the management and running of these conservation facilities (Supplementary Table 2). We identified four groups of participants: (1) representatives of local municipal institutions, (2) researchers who promoted and implemented Ceratozamia conservation through nurseries, (3) members of the community who participated in nursery activities and (4) community members who did not participate (Supplementary Table 2). We also asked members of local communities about their understanding, interpretation and evaluation of conservation strategies (Bennett, Reference Bennett2016). During May–August 2016 we interviewed 10 local residents (nine men and one woman) from different socio-economic backgrounds. The semi-structured interviews lasted 10–30 minutes, and six were audio-recorded. Four participants did not consent to audio recordings; we took detailed notes in these cases. We asked about the participants’ knowledge of the nursery, their level of participation and perceived effects of the nursery on the community (including benefits and conflicts arising during project management). All participants gave oral consent for the use of the information, and their anonymity was preserved. We analysed the interviews qualitatively following standard practices in sociocultural anthropology and ethnobiology, using the characteristics of the content to detect any trends. During the analysis, we attempted to identify any temporal changes in the development of the nurseries (Bernard, Reference Bernard2011; Albuquerque et al., Reference Albuquerque, Fernandes Cruz da Cunha, Farias Paiva de Lucena and Nóbrega-Alvez2014).

Results

Taxonomy of Ceratozamia species in the Sierra Madre Oriental

The distribution of Ceratozamia species in the Sierra Madre Oriental is confined to a narrow eco-climatic zone. In herbaria and during our fieldwork, we found a total of 150 unique records, with geographical coordinates, of the 14 species that occur in this Mexican province. Six species are micro-endemic, of which five are located in the south of the region: C. brevifrons, C. morettii and C. tenuis occur in the Sierra Norte de Puebla-Chiconquiaco region, and C. mexicana is present in the south in a part of the Antigua Basin and, to a lesser extent, in the Huatusco-Coscomatepec area (Fig. 1). Ceratozamia decumbens is distributed in the Huautla-Zongolica region and in a small part of the Orizaba region (Fig. 2), and C. zaragozae is endemic to the Sierra de Álvarez (San Luis Potosí).

Fig. 1 Modelled potential geographical range of two species of Ceratozamia: the widely distributed C. fuscoviridis and the micro-endemic C. tenuis.

Fig. 2 Modelled potential geographical distribution for Ceratozamia: (a) northern area, (b) southern area, (c) central area, (d) Ceratozamia species and subregions of cloud forest in Sierra Madre Oriental.

The remaining eight Ceratozamia species, occurring from the central area to the northern extreme of the region, have a wider distribution (Fig. 1). The species with the northernmost distribution, C. kuesteriana, occurs widely in two regions: El Cielo, and Canyons of Nuevo Leon and Tamaulipas. In the latter location, we did not locate this species during fieldwork. Ceratozamia fuscoviridis and C. totonacorum occur in the cloud forest between San Bartolo Tutotepec (Hidalgo State) and Cuetzalan (Puebla State), and in the north-west from Hidalgo to Huayacocotla in Veracruz (Fig. 2). The distribution of C. totonacorum includes part of the Sierra Norte de Puebla-Chiconquiaco region. Ceratozamia hildae and C. latifolia are located in north-west Hidalgo and as far as Huayacocotla, with vestiges in the San Luis Potosí region; the potential distributions for these two species overlap almost completely. Ceratozamia delucana is restricted to the Sierra Norte de Puebla-Chiconquiaco region and to a small cloud forest area in north-west Hidalgo and Huayacocotla, whereas C. chamberlainii and C. sabatoi inhabit a single forest area (Fig. 2).

Species richness and land use

We observed two areas of particularly high species richness. One was in the northern part of the study area, where five species with wide distributions converge, and for which the model predicted suitable ecological conditions for the presence of up to three additional species. The second area was in the south, with mainly micro-endemic species (Fig. 3). Of the total range of Ceratozamia, 46% has been converted to anthropogenic environments (Fig. 4). Species with the smallest potential range occur in the southern area, which has been largely transformed. Agriculturally driven environmental degradation is most severe within the range of C. mexicana (Table 1); in contrast, undisturbed natural habitats persist in the northern area. Ceratozamia latifolia and C. hildae have a greater potential range in areas with original vegetation (Figs 3 & 4).

Fig. 3 Modelled potential species richness of Ceratozamia and priority biocultural regions for conservation and development.

Fig. 4 Modelled potential species richness of Ceratozamia in the Sierra Madre Oriental (inset: potential geographical distribution of Ceratozamia).

Table 1 The area where each species is predicted to be present, area transformed to anthropogenic landscapes, whether the area is considered a biocultural priority region (Boege, Reference Boege2008), and conservation strategies for Ceratozamia species in the Sierra Madre Oriental, Mexico.

Assessment of conservation status and management strategies

Most Ceratozamia species (92%) are under ex situ conservation in botanical gardens (Table 1). These species occur in seven protected areas (Table 1). The Sierra Gorda Biosphere Reserve contains three species (C. chamberlainii, C. sabatoi and C. hildae). According to their potential range, C. kuesteriana and C. fuscoviridis could occur in the Altas Cumbres Federal Reserve, in the Chicamole ecological preservation municipal area (Fig. 5a), but we were unable to confirm this during fieldwork.

Fig. 5 Modelled potential species richness of Ceratozamia and (a) protected areas, and (b) Priority Terrestrial Regions for Conservation (CONABIO, 2004).

The distribution of Ceratozamia mostly overlaps with several priority areas for conservation, including areas of high species richness in the northern part of the study area. This area is thus of particular importance for the conservation of the genus (Fig. 5b). The range of Ceratozamia in the mountains of the north and central Sierra Madre Oriental, and the southern part of the range of the genus, overlap with three priority biological and cultural areas for conservation and development (Fig. 3). Forests are less affected by anthropogenic pressures in two of these areas (Fig. 4). According to their current categorization in the IUCN Red List (IUCN, 2017) and the Mexican list of threatened species, NOM-059-SEMARNAT-2010 (SEMARNAT, 2010), the species with the highest risk of extinction are those that have experienced less habitat loss. For example, C. kuesteriana has a relatively broad distribution but is categorized as Critically Endangered on the IUCN Red List. In contrast, C. mexicana is categorized as Vulnerable but occurs in an area with rapid loss of habitat (Supplementary Table 3, Figs 2c & 4). This suggests that the extinction risk of these species should be re-evaluated to align the categorization with actual threat levels.

In our survey of the two nurseries, we found that although approaches varied, outcomes were similar. Tachinola nursery is an Ejidal organization (a form of communal property/territory common in rural Mexican regions) in operation since 1995, whereas Dos Cerros nursery is a private initiative that started in 2006 and ceased to operate around 2014. In the case of Tachinola nursery, the conservation actions taken involved seed collections in the wild and transplanting of parental plants from wild populations, to protect them from potential destruction of their habitat. Both nurseries had three goals: (1) conservation of C. tenuis, (2) awareness-raising through social outreach and (3) contribution to the community's economy. Economically, Tlachinola provided benefits in the form of cash payments to community members who participated in cultivation and plant care, and Dos Cerros provided cash payments to community members for helping to transplant Ceratozamia plants, and to nursery managers for carrying out organizational tasks.

In both Tlachinola and Dos Cerros, local informants reported difficulties in the commercialization of plants (few or no sales of cycads) as a cause for the decline of the nurseries. Other reasons included low prices of plants sold, and excessive investment of time in relation to perceived benefits, which is in part because of the slow growth of the species. Overall, attitudes of local people towards Ceratozamia conservation through nurseries were negative. In response to our questions about future development and further outcomes of nursery management, most community informants recognized the failure of these initiatives. We found three additional problems: (1) organizational difficulties caused by lack of agreements between technical researchers and members of the community regarding the sale of plants, (2) lack of direct involvement of the communities in the management and operation of nurseries, and (3) absence of a marketing strategy to commercialize the cycad plants grown in nurseries. Several conflicts within and outside the community affected the work. For example, information on the progress of plant sales was not shared with all members of the community, and restrictions on the use of natural resources were imposed by authorities (use of the species is prohibited, except as ornaments on Catholic altars, and the use of seeds for food).

Our interviews showed that community members and the conservation researchers promoting and implementing conservation through nurseries differed in their conceptual framing of Ceratozamia conservation. Local people perceived conservation as protection of the natural resources on which they depend, whereas researchers viewed conservation primarily as a means of protecting wildlife from extinction.

Discussion

Through a multidisciplinary approach that links ecological and social aspects, we explored current conservation strategies for Ceratozamia, a genus of cycads in Mexico. Our data contribute to the understanding of the limits of conservation efforts, and demonstrate challenges for future studies. We combined an exhaustive review of occurrence records in herbaria with the taxonomic concepts proposed by Martínez-Domínguez et al. (Reference Martínez-Domínguez, Nicolalde-Morejón, Vergara-Silva and Stevenson2018) and found that reliable taxonomic information on Ceratozamia is lacking, which creates difficulties for the assignment of threat categories (Supplementary Table 3).

Limitations of current conservation strategies

Current protected areas cover only a part of the northern area of the Sierra Madre Oriental, the area with the highest potential suitability for Ceratozamia (Fig. 5a). This corresponds with a recent evaluation of the diversity of endemic species in the northern part of the study area (Salinas-Rodríguez et al., Reference Salinas-Rodríguez, Sajama, Gutiérrez-Ortega, Ortega-Báez and Estrada-Castillón2018); however, we found that the main conservation challenges are in the southern region, which was not evaluated in that study. Species in the southern area have restricted ranges, leaving them vulnerable to habitat destruction and extinction (Fig. 1). Across the state of Veracruz, where both diversity and endemism of Ceratozamia species are high, the areas with the highest concentrations of species richness are unprotected (Fig. 5). Despite occurring within a protected area, species such as C. delucana and C. decumbens have lost more than half of their potential habitat to destruction (Table 1).

Anthropogenic land-use changes affect protected areas in the study region (Fig. 4); the southern zone of the Sierra Madre Oriental is one of the most threatened, with severely transformed vegetation (Fig. 3). Therefore, species in the southern zone of the restricted distribution of Ceratozamia require urgent conservation planning. There is considerable overlap between the distribution of Ceratozamia and the main Priority Terrestrial Regions for Conservation (Fig. 4) defined by Mexican authorities. These areas are considered relevant for the conservation of many other plant and animal taxa, but forest cover continues to decline. This suggests that current protected areas are ineffective in conserving species endemic to Mexico. In this context, cycads could serve as biogeographical and ecological model species in conservation biology studies, as they occur in heterogeneous habitats and are frequently associated with other endemic species. In situ conservation actions are required to mitigate the loss of diversity in these cloud forests, which comprise highly diverse and productive ecosystems in Mexico (Gual-Díaz & González-Medrano, Reference Gual-Díaz, González-Medrano, Gual-Díaz and Rendón-Correa2014).

Ex situ conservation initiatives have dominated the preservation of cycads in Mexico, with botanic gardens playing an important role (Griffith et al., Reference Griffith, Calonje, Meerow, Tut, Kramer and Hird2015). However, species that occur in a narrow geographical area, and/or are strictly dioecious, tend to have reduced ranges and populations when their habitats are fragmented by human activities. This leaves them more vulnerable to extinction than species with a broader distribution. Conserving Ceratozamia species and other cycad genera such as Dioon and Zamia requires improved conservation strategies and careful selection of the best strategy depending on the characteristics of the species and the area in which it occurs.

Improving conservation strategies through multidisciplinary approaches

The best preserved areas for Ceratozamia in the Sierra Madre Oriental, which potentially include the highest number of cycad species (except the range of C. decumbens; Fig. 3), correspond with priority biocultural regions. These are territories with long-term occupation by Indigenous peoples and peasant communities of Mesoamerican origin, and are characterized by high levels of biological, agrobiological and cultural diversity (Boege, Reference Boege2008). The fact that these areas harbour a large number of Ceratozamia species could be a result of the past activities of diverse Mesoamerican peoples, who have managed natural resources without destroying or severely damaging the forest (Toledo et al., Reference Toledo, Ortiz-Espejel, Cortés, Moguel and Ordoñez2003). Our findings suggest that, in addition to considering the biology of the target taxa, successful conservation and management of threatened species must enable active and direct participation of local communities. This community engagement should not be limited to the provision of economic benefits during the implementation of conservation projects, but should start during the planning phase, to avoid negative perceptions of, and attitudes towards, conservation and management strategies.

We detected a series of conflicts in the nurseries studied, such as a lack of dialogue between members of the community and researchers, discontent and distrust within the community, difficulty selling the plants, and organizational problems (lack of agreements). In both nurseries, Thachinola and Dos Cerros, members of local communities were considered as employees, rather than principal participants. The nature of these conflicts could vary regionally because of diverse factors (e.g. social values, socio-economic status). Our work could serve as a starting point for a comprehensive analysis of nurseries management. Development of a more complex socio-environmental framework is necessary to plan any further establishment of cycad nurseries in the communities in the study area. We recommend that communities should be involved in conservation planning from the start, as principal actors, in coordination with the developers of planning processes. In addition, the current practice of cultivating a single species could be replaced with diversified models featuring a range of products and practices, such as cultivation of cycads and other species with faster growth rates, or inclusion of recreational activities such as tourist trails.

Overall, our findings suggest that the conservation status of most Ceratozamia species needs to be re-evaluated. In particular, the threat categories used in Mexican legislation need to be updated (Figs 2 & 4). Considering that most cycad species in this area have cultural importance as religious symbols (Bonta et al., Reference Bonta, Pulido-Silva, Diego-Vargas, Vite-Reyes, Vovides and Cibrián-Jaramillo2019), a re-evaluation of the relationship between cycads and people is important for the conservation of this group. We recommend community-managed protected areas to improve conservation effectiveness, and the incorporation of traditional knowledge in the planning and implementation of conservation actions (Berkes, Reference Berkes2009; Shahabuddin & Rao, Reference Shahabuddin and Rao2010). This is particularly applicable in priority areas for biocultural conservation and development that have a high species richness, such as those harbouring C. sabatoi, C. hildae, C. kuesteriana, C. zaragozae and C. fuscoviridis (Fig. 3). Working at the scale of ecosystem conservation, several studies have pointed out the need to combine approaches from basic and applied and/or social science, and to apply a holistic perspective to complex problems (Lindenmayer & Hunter, Reference Lindenmayer and Hunter2010). Biodiversity conservation requires both information on species’ biology, and acceptance of science-based programmes by communities, whose priorities and viewpoints need to be considered. Conservation strategies thus need to be evaluated from a multidisciplinary perspective, through assessment of ecological and taxonomic issues combined with an examination of social perceptions. Such collaborative approaches have the potential to improve the effectiveness of ex situ conservation strategies for Ceratozamia and other taxa.

Acknowledgements

This research was supported in part by Consejo Nacional de Ciencia y Teconología under grant 134960 to FNM, and National Science Foundation grants BSR-8607049 and EF-0629817 to DWS. LMD thanks CONACYT for the award of a Masters degree scholarship. We thank C. Yañez-Arenas and S. Jiménez-García for advice on ecological niche modelling and the socio-cultural anthropology aspects, respectively; the curators of all herbaria; the communities in the municipality of Coacoatzintla for their cooperation; the anonymous reviewers for their constructive critiques; and the editors for their extensive help in finalizing the text.

Author contributions

Study design: LMD, FNM, FVS; data collection: LMD, FNM; data analysis: LMD, FNM, ORS; writing and revisions: all authors.

Conflicts of interest

None.

Ethical standards

We obtained permission to conduct this research within the community from community representatives, and informed consent from interviewees. This research complied with the Oryx guidelines on ethical standards and the Ethical Code of the American Sociological Association.

Footnotes

Supplementary material for this article is available at doi.org/10.1017/S0030605320000204

*

Also at: Centro de Investigaciones Tropicales, Universidad Veracruzana, Xalapa, Veracruz, Mexico

References

Albuquerque, U.P., Fernandes Cruz da Cunha, L.V., Farias Paiva de Lucena, R. & Nóbrega-Alvez, R.R. (2014) Methods and Techniques in Ethnobiology and Ethnoecology. Humana Press/Springer, New York, USA.10.1007/978-1-4614-8636-7CrossRefGoogle Scholar
Barve, N. (2008) Tool for Partial-ROC, version 1.0. Biodiversity Institute, Lawrence, USA.Google Scholar
Barve, N. & Barve, V. (2013) ENMGadgets: Tools for Pre and Post Processing in ENM Workflows. github.com/vijaybarve/ENMGadgets [accessed 26 June 2020].Google Scholar
Barve, N., Barve, V., Jiménez-Valverde, A., Lira-Noriega, A., Mahera, S.A., Peterson, A.T. et al. (2011) The crucial role of the accessible area in ecological niche modeling and species distribution modeling. Ecological Modelling, 222, 18101819.CrossRefGoogle Scholar
Bennett, N.J. (2016) Using perceptions as evidence to improve conservation and environmental management. Conservation Biology, 30, 582592.CrossRefGoogle ScholarPubMed
Berkes, F. (2009) Community conserved areas: policy issues in historic and contemporary context. Conservation Letters, 2, 1924.CrossRefGoogle Scholar
Bernard, H.R. (2011) Research Methods in Anthropology. Qualitative and Quantitative Approaches, 5th edition. AltaMira Press, Plymouth, UK.Google Scholar
Boege, E. (2008) El Patrimonio Biocultural de los Pueblos Indígenas de México, 1st edition. Instituto Nacional de Antropología e Historia, Comisión Nacional para el Desarrollo de los Pueblos Indígenas, Mexico City, Mexico.Google Scholar
Bonta, M., Pulido-Silva, M.T., Diego-Vargas, T., Vite-Reyes, A., Vovides, A.P. & Cibrián-Jaramillo, A. (2019) Ethnobotany of Mexican and northern Central American cycads (Zamiaceae). Journal of Ethnobiology and Ethnomedicine, 4, 15.Google Scholar
Bottrill, M.C. & Pressey, R.L. (2012) The effectiveness and evaluation of conservation planning. Conservation Letters, 5, 407420.10.1111/j.1755-263X.2012.00268.xCrossRefGoogle Scholar
Calabrese, J.M., Certain, G., Kraan, C. & Dormann, C.F. (2014) Stacking species distribution models and adjusting bias by linking them to macroecological models. Global Ecology and Biogeography, 23, 99112.CrossRefGoogle Scholar
Calonje, M., Stevenson, D.W. & Osborne, R., (2019) The World List of Cycads, online edition. cycadlist.org [accessed 20 September 2019].Google Scholar
CITES (2019) Convención Sobre el Comercio Internacional de Especies Amenazadas de Fauna y Flora Silvestres. CITES, Gevena, Switzerland. cites.org/esp/disc/text.php [accessed 27 October 2019].Google Scholar
CONABIO (2004) Regiones Terrestres Prioritarias. Escala 1:1000000. Comisión Nacional para el Conocimiento y Uso de la Biodiversidad (CONABIO), Mexico City, Mexico. conabio.gob.mx/informacion/gis [accessed 27 May 2017].Google Scholar
CONABIO (2008) Principales Regiones y Subregiones del Bosque Mesófilo de Montaña en México. Comisión Nacional para el Conocimiento y Uso de la Biodiversidad (CONABIO), Mexico City, Mexico. conabio.gob.mx/informacion/gis [accessed 20 May 2018].Google Scholar
CONABIO (2015) Áreas Naturales Protegidas Estatales, Municipales, Ejidales y Privadas de México, 1st edition. Comisión Nacional para el Conocimiento y Uso de la Biodiversidad (CONABIO), Mexico City, Mexico. conabio.gob.mx/informacion/gis [accessed 25 May 2017].Google Scholar
CONANP (2014) Áreas Naturales Protegidas Federales de México. Escala: 1:0, 1st edition. Comisión Nacional de Áreas Naturales Protegidas (CONANP), Mexico City, Mexico. conabio.gob.mx/informacion/gis [accessed 25 May 2017].Google Scholar
Contreras-Medina, R. (2004) Gimnospermas. In Biodiversidad de la Sierra Madre Oriental (eds Luna, I., Morrone, J.J. & Espinosa-Organista, D.), pp. 137148. National Autonomous University of Mexico, Mexico City, Mexico.Google Scholar
D'Amen, M., Dubuis, A., Fernandes, R.F., Pottier, J., Pellissier, L. & Guisan, A. (2015a) Using species richness and functional traits predictions to constrain assemblage predictions from stacked species distribution models. Journal Biogeography, 42, 12551266.CrossRefGoogle Scholar
D'Amen, M., Pradervand, J.N. & Guisan, A. (2015b) Predicting richness and composition in mountain insect communities at high resolution: a new test of the SESAM framework. Global Ecology Biogeography, 24, 14431453.CrossRefGoogle Scholar
Donaldson, J.S. (2003) Cycads: Status Survey and Conservation Action Plan. IUCN/SSC Cycad Specialist Group, IUCN, Gland, Switzerland and Cambridge, UK.Google Scholar
Eguiluz de Antuñano, S., Aranda-García, M. & Marrett, R. (2000) Tectónica de la Sierra Madre Oriental, México. Boletín de la Sociedad Geológica Mexicana, LIII, 126.CrossRefGoogle Scholar
Elith, J., Kearney, M. & Phillips, S.J. (2010) The art of modelling range-shifting species. Methods in Ecology and Evolution, 1, 330342.CrossRefGoogle Scholar
Graham, D.A., Bonta, M.A. & Ulloa, R. (2011) Cycad conservation, peasant subsistence, and the military coup in Honduras. Society and Natural Resources, 24, 193200.CrossRefGoogle Scholar
Griffith, M.P., Calonje, M., Meerow, A.W., Tut, F., Kramer, A.T., Hird, A. et al. (2015) Can a botanic garden cycad collection capture the genetic diversity in a wild population? International Journal of Plant Science, 176, 110.CrossRefGoogle Scholar
Gual-Díaz, M. & González-Medrano, F. (2014) Los bosques mesófilos de montaña en México. In Bosques Mesófilos de Montaña de México: Diversidad, Ecología y Manejo (eds Gual-Díaz, M. & Rendón-Correa, A.), pp. 2767. Comisión Nacional para el Conocimiento y Uso de la Biodiversidad (CONABIO), Mexico City, Mexico.Google Scholar
Halme, P., Kuusela, S. & Juslén, A. (2015) Why taxonomists and ecologists are not, but should be, carpooling? Biodiversity and Conservation, 24, 18311836.CrossRefGoogle Scholar
Hijmans, R.J., Cameron, S.E., Parra, J.L., Jones, P.G. & Jarvis, A. (2005) Very high resolution interpolated climate surfaces for global land areas. International Journal of Climatology, 25, 19651978.10.1002/joc.1276CrossRefGoogle Scholar
Hijmans, R.J., Phillips, S.J., Leathwick, J. & Elith, J. (2011) Dismo: Species Distribution Modeling, R Package, version 0.7–17. CRAN. R-project.org/package=dismo [accessed November 2020].Google Scholar
Holt, R.D. (2009) Bringing the Hutchinsonian niche into the 21st century: ecological and evolutionary perspectives. Proceedings of the National Academy of Science of the United States of America, 106, 1965919665.CrossRefGoogle ScholarPubMed
INEGI (2013) Uso del Suelo y Vegetación Escala 1:250 000, serie V. Instituto Nacional de Estadística y Geografía (INEGI), Mexico City, Mexico. conabio.gob.mx/informacion/gis [accessed 25 February 2017].Google Scholar
IUCN (2017) The IUCN Red List of Threatened Species. IUCN, Gland, Switzerland. iucnredlist.org [accessed 13 December 2017].Google Scholar
Lindenmayer, D. & Hunter, M. (2010) Some guiding concepts for conservation biology. Conservation Biology, 24, 14591468.CrossRefGoogle ScholarPubMed
Martínez-Domínguez, L., Nicolalde-Morejón, F., Vergara-Silva, F. & Stevenson, D.W. (2018) Taxonomic review of Ceratozamia (Zamiaceae) in the Sierra Madre Oriental, Mexico. PhytoKeys, 100, 91124.CrossRefGoogle Scholar
Mota-Vargas, C. & Rojas-Soto, O. (2012) The importance of defining the geographic distribution of species for conservation: the case of the bearded wood-partridge. Journal for Nature Conservation, 20, 1017.CrossRefGoogle Scholar
Mota-Vargas, C. & Rojas-Soto, O. (2016) Taxonomy and ecological niche modeling: implications for the conservation of wood partridges (genus Dendrortyx). Journal of Nature Conservation, 29, 113.CrossRefGoogle Scholar
Nicolalde-Morejón, F., González-Astorga, J., Vergara-Silva, F., Stevenson, D.W., Rojas-Soto, O. & Medina-Villarreal, A. (2014) Biodiversidad de Zamiaceae en México. Revista Mexicana de Biodiversidad, 85, S114S125.10.7550/rmb.38114CrossRefGoogle Scholar
Norstog, K.J. & Nicholls, T.J. (1997) The Biology of the Cycads. Cornell University Press, Ithaca, USA.Google Scholar
Orlove, B.S. & Brush, S.B. (1996) Anthropology and the conservation of biodiversity. Annual Review Anthropology, 25, 329352.CrossRefGoogle Scholar
Paniagua, L. & Morrone, J.J. (2009) Do the Oaxacan Highlands represent a natural biotic unit? A cladistic biogeographical test based on vertebrate taxa. Journal of Biogeography, 36, 19391944.CrossRefGoogle Scholar
Pearson, R.G., Raxworthy, C.J., Nakamura, M. & Peterson, T. (2007) Predicting species distributions from small numbers of occurrence records: a test case using cryptic geckos in Madagascar. Journal of Biogeography, 34, 102117.CrossRefGoogle Scholar
Peterson, A.T. & Soberón, J. (2012) Species distribution modeling and ecological niche modeling: getting the concepts right. Natureza & Conservacao, 10, 16.CrossRefGoogle Scholar
Peterson, A.T., Sánchez-Cordero, V., Martínez-Meyer, E. & Navarro-Sigüenza, A.G. (2006) Tracking population extirpations via melding ecological niche modeling with land-cover information. Ecological Modelling, 195, 229236.CrossRefGoogle Scholar
Peterson, A.T., Papes, M. & Soberón, J. (2008) Rethinking receiver operating characteristic analysis applications in ecological niche modelling. Ecological Modelling, 213, 6372.CrossRefGoogle Scholar
Phillips, S.J., Anderson, R.P. & Schapired, R.E. (2006) Maximum entropy modeling of species geographic distributions. Ecological Modelling, 190, 231259.CrossRefGoogle Scholar
R Development Core Team (2012) R: A Language and Environment for Statistical Computing. The R Foundation for Statistical Computing, Vienna, Austria.Google Scholar
Salinas-Rodríguez, M.M., Sajama, M.J., Gutiérrez-Ortega, J.S., Ortega-Báez, P. & Estrada-Castillón, A.E. (2018) Identification of endemic vascular plant species hotspots and the effectiveness of the protected areas for their conservation in Sierra Madre Oriental, Mexico. Journal for Nature Conservation, 46, 627.CrossRefGoogle Scholar
Semarnat (2010) Norma Official Mexicana NOM-059-SEMARNAT-2010. Secretaría de Medio Ambiente y Recursos Naturales (SEMARNAT), Mexico City, Mexico. profepa.gob.mx/innovaportal/file/435/1 [accessed 25 February 2017].Google Scholar
Shahabuddin, G. & Rao, M. (2010) Do community-conserved areas effectively conserve biological diversity? Global insights and the Indian context. Biological Conservancy, 143, 29262936.CrossRefGoogle Scholar
Thiers, B. (2019) Index Herbariorum. A Worldwide Index of 3,100 Herbaria and 12,000 Associated Staff where a Total of 390 Million Botanical Specimens are Permanently Housed. New York Botanical Garden's Virtual Herbarium. sweetgum.nybg.org/science/ih [accessed November 2020].Google Scholar
Toledo, V.M., Ortiz-Espejel, B., Cortés, L., Moguel, P. & Ordoñez, M.D.J. (2003) The multiple use of tropical forests by Indigenous peoples in Mexico: a case of adaptive management. Conservation Ecology, 7, 9.CrossRefGoogle Scholar
Vovides, A.P. & Iglesias, C.G. (1994) An integrated conservation strategy for the cycad Dioon edule Lindl. Biodiversity and Conservation, 3, 137141.CrossRefGoogle Scholar
Vovides, A.P., Pérez-Farrera, M.A., Vázquez-Torres, M. & Schippmann, U. (2002) Peasant nurseries: a concept for an integrated conservation strategy for cycads in Mexico. In Plant Conservation in the Tropics: Perspectives and Practice (eds Maunder, M., Clubbe, C., Hankamer, C. & Groves, M.), pp. 421444. Royal Botanic Gardens, Kew, UK.Google Scholar
Vovides, A.P., Pérez-Farrera, M.A. & Iglesias, C. (2010) Cycad propagation by rural nurseries in Mexico as an alternative conservation strategy: 20 years on. Kew Bulletin, 65, 603611.CrossRefGoogle Scholar
Wheeler, Q.D., Knapp, S., Stevenson, D.W., Stevenson, J., Blum, S.D., Boom, B.M. et al. (2012) Mapping the biosphere: exploring species to understand the origin, organization and sustainability of biodiversity. Systematic Biodiversity, 10, 120.CrossRefGoogle Scholar
Figure 0

Fig. 1 Modelled potential geographical range of two species of Ceratozamia: the widely distributed C. fuscoviridis and the micro-endemic C. tenuis.

Figure 1

Fig. 2 Modelled potential geographical distribution for Ceratozamia: (a) northern area, (b) southern area, (c) central area, (d) Ceratozamia species and subregions of cloud forest in Sierra Madre Oriental.

Figure 2

Fig. 3 Modelled potential species richness of Ceratozamia and priority biocultural regions for conservation and development.

Figure 3

Fig. 4 Modelled potential species richness of Ceratozamia in the Sierra Madre Oriental (inset: potential geographical distribution of Ceratozamia).

Figure 4

Table 1 The area where each species is predicted to be present, area transformed to anthropogenic landscapes, whether the area is considered a biocultural priority region (Boege, 2008), and conservation strategies for Ceratozamia species in the Sierra Madre Oriental, Mexico.

Figure 5

Fig. 5 Modelled potential species richness of Ceratozamia and (a) protected areas, and (b) Priority Terrestrial Regions for Conservation (CONABIO, 2004).

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