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Piloting development of species conservation action plans in Guinea

Published online by Cambridge University Press:  20 October 2022

Charlotte Couch
Affiliation:
Royal Botanic Gardens, Kew, Richmond, UK
Denise Molmou
Affiliation:
Herbier National de Guinée, Université Gamal Abdel Nasser de Conakry, BP1147, Conakry, Guinea
Sékou Magassouba*
Affiliation:
Royal Botanic Gardens, Kew, Richmond, UK
Saïdou Doumbouya
Affiliation:
Ministre de l'Environnement, Eaux et Forêts, République de Guinée, Conakry, Guinea
Mamadou Diawara
Affiliation:
Guinée Ecologie, Dixinn, Conakry, Guinea
Muhammad Yaya Diallo
Affiliation:
Guinée Ecologie, Dixinn, Conakry, Guinea
Sékou Moussa Keita
Affiliation:
Centre d'Etudes de Recherche en Environnement, Université Gamal Abdel Nasser de Conakry, Conakry, Guinea
Falaye Koné
Affiliation:
Ministre de l'Environnement, Eaux et Forêts, République de Guinée, Conakry, Guinea
Mahamadou Cellou Diallo
Affiliation:
Protection et Gestion de l'Environnement, Conakry, Guinea
Sékou Kourouma
Affiliation:
Ministre de l'Environnement, Eaux et Forêts, République de Guinée, Conakry, Guinea
Mamadou Bella Diallo
Affiliation:
Ministre de l'Environnement, Eaux et Forêts, République de Guinée, Conakry, Guinea
Mamady Sayba Keita
Affiliation:
Ministre de l'Environnement, Eaux et Forêts, République de Guinée, Conakry, Guinea
Aboubacar Oularé
Affiliation:
Ministre de l'Environnement, Eaux et Forêts, République de Guinée, Conakry, Guinea
Iain Darbyshire
Affiliation:
Royal Botanic Gardens, Kew, Richmond, UK
George Gosline
Affiliation:
Royal Botanic Gardens, Kew, Richmond, UK
Eimear Nic Lughadha
Affiliation:
Royal Botanic Gardens, Kew, Richmond, UK
Xander van der Burgt
Affiliation:
Royal Botanic Gardens, Kew, Richmond, UK
Isabel Larridon
Affiliation:
Royal Botanic Gardens, Kew, Richmond, UK
Martin Cheek
Affiliation:
Royal Botanic Gardens, Kew, Richmond, UK
*
(Corresponding author, [email protected])

Abstract

Conservation action plans need to be devised and implemented if we are to reduce the extinction risk faced by globally threatened plants. However, most plant species categorized as threatened globally on the IUCN Red List lack conservation action plans. In West Africa, Guinea is one of the most diverse countries in terms of botanical species. In total, 273 plant species in Guinea have been assessed as being threatened globally, reflecting increasing pressure from the extractive industry and a growing population requiring food and fuel. In parallel with the implementation of an Important Plant Area programme in Guinea, we developed conservation action plans for 20 threatened plant species through a pilot study. We outline the methods we used and demonstrate the importance of adopting a collaborative approach and having up-to-date field information. The need for such plans is urgent, with recent estimates suggesting that one-third of African plants are threatened with extinction. Based on our experience with the first 20 conservation action plans for Guinea species, we suggest that the preparation of multi-species conservation action plans would be an efficient use of the limited resources available for species conservation.

Type
Article
Creative Commons
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This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://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), 2022. Published by Cambridge University Press on behalf of Fauna & Flora International

Introduction

Conservation scientists seek to identify and protect globally threatened species and achieve species recovery. The impacts of conservation actions are recorded in terms of extinctions avoided (e.g. Bolam et al., Reference Cheek2021; Grace et al., Reference Couch, Molmou and Magassouba2021) or using other metrics such as Green Status (Akçakaya et al., Reference Akçakaya, Bennett, Brooks, Grace, Heath and Hedges2018; IUCN, Reference Couch, Molmou and Magassouba2021a). The IUCN has published seven conservation action plans concerning plants: six taxon-based and one area-based. These plans address taxa or areas encompassing c. 65,000 species, most of which have not been assessed but are unlikely to be threatened. The total number of globally threatened species specified in five of the taxon-based plans is 4,872. This accounts for only 22% of the threatened species on the IUCN Red List (IUCN, Reference Couch, Molmou and van der Burgt2021b). To help address this deficit, we conducted a pilot study to develop conservation action plans for threatened plant species in Guinea, West Africa. We discuss insights derived from this process, which could inform the development of conservation action plans by conservation practitioners in other tropical African countries.

In West Africa, Guinea is one of the most diverse countries in terms of botanical species. According to our recent analysis (G. Gosline, unpubl. data, 2021) there are 826 additional recorded angiosperm taxa at the species or infra-specific level in Guinea in addition to the c. 3,000 species that have already been listed (Lisowski, Reference Goyder2009). This increase in the number of species reflects extensive research to inventory the flora of Guinea through the digitization of historical herbarium records (Magassouba et al., Reference Grace, Akçakaya, Bennett, Brooks, Heath and Hedges2014; GBIF, Reference Couch, Molmou and Magassouba2019), complemented by targeted field expeditions to understudied areas of Guinea by the staff of the National Herbarium of Guinea and the Royal Botanic Gardens, Kew (hereafter Kew; Cheek & Magassouba, Reference Cheek, Poveda and Molmou2018; Cheek et al., Reference Correia, Diabaté, Beavogui, Guilavogui, Lamanda and de Foresta2018; van der Burgt et al., Reference Molmou and Couch2018, Reference Molmou and Couch2019b).

The comparatively high plant diversity in Guinea reflects its variety of species-rich habitats and the isolation of its highland areas. For example, the central Fouta Djallon highlands have 42 endemic plant species in a variety of habitats such as sandstone cliffs, sandstone and ferralitic bowal (treeless hardpan) and submontane forest (Couch et al., Reference Couch and Molmou2019a). However, over centuries this area has undergone significant changes because of the expansion of agricultural systems. Intact submontane forest has now largely disappeared from the Fouta Djallon (Lebbie, 2001). A recent 3-year project to identify Tropical Important Plant Areas in Guinea (Couch et al., Reference Couch and Molmou2019a) showed that of 35 threatened species not seen by botanists for 60 years or more, 25 are endemic to Guinea and 19 occur in the Fouta Djallon. Despite targeted searches, Habenaria jaegeri and Kotschya lutea have not been seen in the Fouta Djallon for 57 and 82 years, respectively, and are considered extinct there.

The Tropical Important Plant Areas of Guinea project identified nine threatened habitats and delineated 22 Tropical Important Plant Areas (Couch et al., Reference Couch and Molmou2019a). Tropical Important Plant Areas (Royal Botanic Gardens, Kew, 2016) are assessed using three criteria: the presence of (1) threatened species, (2) botanical richness (including species of socio-economic interest) and (3) threatened habitats (Darbyshire et al., Reference Couch and Molmou2017). Each Tropical Important Plant Area assessment also documents past, present and future threats as well as current protection. A variety of threats endanger the flora of Guinea, including mining. Guinea is one of the leading exporters of bauxite, exporting 95% of the African and 15% of the global production of bauxite (Sengupta, Reference Sengupta2019). It also has considerable reserves of iron ore, gold and diamonds (Guinean Ministry of Mines and Geology, Reference Couch, Molmou and Magassouba2016). However, for many of the country's habitats, in particular the lowland evergreen forest and submontane forest, the main threats are unsustainable agricultural practices and the cutting of wood for charcoal. By the late 20th century, 96% of Guinea's original forest had disappeared (Sayer et al., 1992). In the bowal areas, the main threats are from cattle-ranging practices that increase the frequency of fires.

Funding and governance provisions for new large-scale projects (e.g. in the mining sector and for hydroelectric power) require companies to carry out detailed social and environmental impact assessments. These studies involve the identification of threatened plant species. Specifically, Performance Standard 6 of the International Finance Corporation (on Biodiversity Conservation and Sustainable Management of Living Natural Resources) requires concession holders to identify any areas of Critical Habitat. This definition includes habitats of significant importance to Critically Endangered and/or Endangered species. Project activities must not be implemented in such areas unless they demonstrably do not lead to a net reduction in the global and/or national/regional population of any threatened species. To date, only 13% of plant species have been assessed globally for the IUCN Red List (IUCN, Reference Couch, Molmou and van der Burgt2021b), including almost one-third (29%) of the Guinean flora; therefore, the majority of species await assessment. Thus, decisions continue to be made based on incomplete data, risking the possibility of a net reduction in populations of threatened species and in Critical Habitat over time.

The past 5 years have seen an increasing focus on documenting the extinction risk of the Guinean flora. In 2016, the project ‘Towards a Red Data Book for Guinea’, in collaboration with the Darwin Initiative-funded Tropical Important Plant Area project, assessed c. 200 plant species from Guinea using the IUCN Red List Categories and Criteria (IUCN, 2012b). A preliminary list of threatened plant species for Guinea was produced in 2017 and revised throughout the implementations of these projects (Couch et al., Reference Couch and Molmou2019b) to update stakeholders ahead of the publication of a comprehensive Red Data Book for all threatened plants of Guinea. This list will also be incorporated into an update of the Monographie Nationale (Guinea's national biodiversity management action plan), which has not been revised since 1997. The process of inclusion in the Red List involves the documentation of recommended, ongoing and required conservation actions. However, these are high-level actions that usually lack the level of detail required for planning or implementing concrete conservation actions.

We conducted a pilot study to trial the development of individual species conservation action plans for 20 plant species assessed as threatened on the IUCN Red List. These plans recommend the conservation actions needed to safeguard each of these threatened species both in situ and ex situ. Here we outline the methods piloted to assemble the first 20 species conservation action plans for Guinean plants. We demonstrate the importance of having up-to-date field information and adopting a collaborative approach and how these action plans will improve conservation efforts in Guinea. We also consider how the implementation of these plans could lead to greater recognition of plant conservation needs both in Guinea and regionally in West Africa.

Methods

The preparation of species conservation action plans must take into consideration several key questions, the first being: who should be involved in this process? To address this, a joint working group to advance the assessment of Tropical Important Plant Areas and the preparation of conservation action plans was formed in May 2018. The working group brought together for the first time representatives from the National Herbarium of Guinea, Kew, the Guinean Ministry of Environment, Water and Forests, the National Parks and Reserves Office, the Centre for Biological Observations and Monitoring, the environmental NGOs Guinée Ecologie and Protection et Gestion de l'Environnement, the Centre for Environmental Research Studies at the Université Gamal Abdel Nasser de Conakry and the Sérédou Herbarium (Institut de Recherche Agronomique de Guinée).

We drafted the protocol for preparing the plans prior to the establishment of the working group, and the protocol was subsequently discussed and approved by the group (Couch, Reference Couch2019). The protocol was based in part on the experience of CC in writing similar plans in Mauritius and also on the Conservation Action Planning Handbook (The Nature Conservancy, Reference Lisowski2007), which has been used in tropical Asia, Latin America, Micronesia, the Caribbean and the USA. The format and style drew upon earlier species recovery plans for non-Guinean taxa (JNCC UK Reference Couch, Molmou, van der Burgt and Magassouba2010a,Reference Darbyshire, Anderson, Asatryan, Byfield, Cheek and Clubbeb; Panjabi et al., 2011), informed by the range of potential conservation actions identified during the extinction risk assessment process for relevant species. The group became aware of the Botanic Gardens Conservation International (BGCI) and International Association of Botanic Gardens (IABG) Species Recovery Manual (Heywood et al., Reference Heywood, Shaw, Harvey-Brown and Smith2018) only after the protocol had been agreed and adopted for the drafting of the first plans.

We drew up a shortlist of candidate species for the development of conservation action plans from the preliminary list of 273 Guinean threatened species (Couch et al., Reference Couch and Molmou2019b). The 20 species chosen were categorized as threatened and had completed IUCN Red List assessments that had undergone peer review, although not all had yet been published on the Red List. Species were selected from a range of taxa across a variety of threatened habitats (Table 1).

Table 1 List of species chosen for conservation action plans, with the IUCN Red List status (IUCN, 2021c), growth form and collection data in Guinea resulting from recent fieldwork. See supplementary materials for links to individual conservation action plans.

1 CR, Critically Endangered; EN, Endangered; VU, Vulnerable.

2 Includes verified georeferenced observations.

The first section of each conservation action plan sets out the context for the focal species, including nomenclature, morphology, ecology, phenology, habitat and uses, as well as geographical distribution and population details if available. Existing documentation on Guinean flora is incomplete and often outdated. Many already listed names (Lisowski, Reference Goyder2009) are out of date (Cheek et al., Reference Couch, Molmou, Camara, Cheek, Merklinger and Davies2015) as they are based on the Flora of West Tropical Africa (Keay & Hepper, Reference Fischer, Darbyshire and Cheek1954–1972). Use of these already listed names (Lisowski, Reference Goyder2009) and older documents has perpetuated the use of outdated names or synonyms by Guinean researchers in reports and policy documents. Subsequently, field surveys have led to the discovery of more than 20 species previously unknown to science, all endemic to Guinea (Cheek & Haba, Reference Cheek, Magassouba, Howes, Dore, Doumbouya and Molmou2016; Phillipson et al., 2019; Xanthos et al., Reference Nic Lughadha, Bachman, Leão, Forest, Halley and Moat2020). Furthermore, numerous herbarium specimens collected during 2015–2019 in Guinea have been recognized as representing extensions to the known ranges of species not previously recorded there.

Desk-based research was vital to complement fieldwork, to ensure the focal species were clearly defined, mitigating the risk of scarce conservation resources being directed towards taxonomically doubtful entities. When we prepared an action plan for a recently described species, we used the protologue (original scientific publication) as the primary source for the taxonomic information, including the species circumscription. For other species, we used the Flora of West Tropical Africa as the default source of species circumscriptions, which were then updated using more recent publications focused on these species where available. Descriptions of the plant species were taken from either Lisowski (Reference Goyder2009) or the protologues of newly described species. We collated data largely from herbarium specimen labels. Names were checked against the African Plant Database (2019), the International Plant Names Index (2019) and Plants of the World Online (2022).

Each action plan includes geographical distribution data, particularly within Guinea, including historical records and, where known, the number of individuals in the population or in each subpopulation. We produced a specimen-based distribution map for each species using ArcGIS Pro 2.9 (Esri, Redlands, USA), with simple x, y coordinates uploaded and mapped onto a world base map (Fig. 1).

Fig. 1 The known distribution of four endemic Guinean species: (a) Anisotes guineensis, (b) Talbotiella cheekii, (c) Diospyros feliciana and (d) Eriosema triformum.

The first part of each plan includes information on threats both past and present, and both direct and indirect, gathered from literature and from > 20 field expeditions carried out during 2016–2019, targeting rare species and priority threatened habitats. We aligned the threats with the IUCN threat categories (IUCN, Reference Couch, Molmou and Magassouba2012a,Reference Couch, Molmou and Magassoubab). The second part of each plan sets out a summary plan for the management and conservation of the species. Details are provided of any protected areas in which the species is currently found and whether the species is present within any of the newly designated Tropical Important Plant Areas (Couch et al., Reference Couch and Molmou2019a). In situ and ex situ conservation actions are then proposed for the protection of the species.

Recommendations for in situ conservation include carefully documenting the size, location and condition of the site and the number(s) of mature individuals in the (sub)population(s) present there. These data can be used to support the legal protection of the sites and species. They serve as a baseline for future monitoring of both sites and species and inform future adaptive management planning, amongst other uses.

Proposed ex situ conservation actions focus on the propagation of the species outside its range, including seed collection and banking where applicable, and the potential for translocation to a protected area or botanical garden. The results of any propagation or translocation experiments previously undertaken are also documented for future reference.

Results

The 20 conservation action plans produced during this pilot study represent 7% of the threatened species of Guinea (Supplementary Material 1) and 0.5% of its total flora. Of the 273 threatened species of the flora of Guinea (7% of the total number of species), 25% are woody (10% being widespread timber species) and the remainder are herbaceous or climbing species. In this pilot study we developed plans for eight woody species (including two widespread timber species) one climbing species and 11 herbaceous species. Eleven of these concern species endemic to Guinea; this represents 15% of the 77 plant species considered to be endemic. The over-representation of endemic species in our study reflects the concern of the working group to maximize the protection of those plant species for which Guinea has unique responsibility.

The 20 species are subject to eight main types of threat (Fig. 2). The threats affecting most of these species are: increase in fire frequency (7.1.1; 75%), mining and quarrying (3.2; 60%), wood harvesting (5.3; 45%) and urbanization (1.1; 40%). Two of the species are directly threatened by pollution (9) and all of the woody species (8) are threatened by clearance of habitat (e.g. 2.1.1 shifting agriculture or wood harvesting).

Fig. 2 Per cent of the 20 species for which we prepared conservation action plans (Table 1) subject to each of eight threat types of the IUCN Threat Classification Scheme (IUCN, 2012a).

Nine of the 20 selected species are found in at least one current protected area and all of the species are present within one or more of the newly designated Tropical Important Plant Areas. However, these areas either lack management plans or have management plans that are outdated and lack specificity regarding the species conservation actions needed for plants.

Eight of the selected species have seed collections banked in Guinea at the National Herbarium of Guinea or with Simfer S.A. (a mining company), and the Millennium Seed Bank at Wakehurst, UK. Four of these (Cailliella praerupticola, Habenaria jaegeri, Pitcairnia feliciana and Pterocarpus erinaceus) have reached the recommended seed banking target threshold of 10,000 seeds (Way & Gold, Reference Nganje, Lebbie, Sambollah and Waugh2014), but no data are available as to the extent to which they are genetically representative of their source populations. We trained seed collectors to ensure that genetic variation across the population was captured. Some seed collections are small because there are few known individuals or individuals do not produce many seeds each season. Some species have large seeds and are expected to be recalcitrant (i.e. they are unsuitable for conventional seed banking) because the seeds die when dried (e.g. Talbotiella cheekii). Tarenna hutchinsonii and Keetia susu are probably recalcitrant but remain untested.

For the majority of the selected species no propagation information is available and therefore experimentation will be required. However, for 25% of the species propagation protocols had previously been developed as part of mitigation measures for Simfer S.A. These protocols were researched using a variety of methods (e.g. micropropagation for H. jaegeri (Cheek, Reference Cheek and Williams2017) and cuttings for T. hutchinsonii (Cheek et al., Reference Couch, Molmou, Camara, Cheek, Merklinger and Davies2015) and Marsdenia exellii (Cheek, Reference Cheek and Magassouba2013). Currently, only five of the 20 species have been identified as suitable for potential reintroduction.

Compilation and refinement of the 20 conservation action plans took place over a period of 9 months and the time invested was estimated to be 1,200 person-hours (i.e. 60 h per plan). This total excludes fieldwork because the fieldwork targeted many more species than the 20 selected. However, the importance of recent fieldwork as a foundation for the preparation of conservation action plans became evident in the course of our work. Table 1 documents the contributions of recent fieldwork to our knowledge of the target species. Fieldwork since 2000 enabled the rediscovery of 10 of the selected species, which had not been observed by scientists for several decades. Three endemic species (Anisotes guineensis, Diospyros feliciana and C. praerupticola) were recollected from their original historical locality after 61, 60 and 79 years, and recorded at five, seven and seven additional sites, respectively. Four of the selected species were described as new to science in the past decade, first collected during 2012–2018, and a further four species are new records for Guinea, since 2008, of species previously known only from other countries (i.e. range extensions). Thus, all but two of the conservation action plans were influenced significantly by data resulting from fieldwork conducted during the past decade.

Discussion

The projects Towards a Red Data Book for Guinea and Tropical Important Plant Areas of Guinea have attracted the attention of both national and international audiences to the threatened and unique plant species of the country. The conservation action plans resulting from these projects are the first to be written for threatened plant species in Guinea and are a result of the growing collaboration between the members of the working group. The partnerships and expertise on plant conservation built during these projects did not exist previously. Following the conclusion of both projects in March 2019, the working group has continued to collaborate to address, review and contribute to government policy. The collaboration has gained support from all sectors concerned with plant conservation, and through the publicity for the recently identified Tropical Important Plant Areas (Couch et al., Reference Couch and Molmou2019a) it is promoting plant conservation in Guinea on the national agenda. To the best of our knowledge, this is the first time that such a programme for globally threatened plant species has been devised and acted upon in a West African country.

The 20 species conservation action plans highlight the importance of fieldwork for providing up-to-date information on target species. IUCN Red List assessments can be written based on literature and herbarium records but knowing the status of a population and the current threats the species faces is invaluable when writing a conservation action plan. For most of the plants in our study, conservation action plans developed without these recent field data would be, at best, less useful than they could be and, at worst, irrelevant. Fieldwork has facilitated better population estimates and the identification of suitable areas for protection as Tropical Important Plant Areas. The identification of subpopulations will improve ex situ conservation measures by facilitating the capture of genetic diversity across the population.

The implementation of these plans is the next stage in this process. The plan for Vernonia djalonensis (Supplementary Material 1) has already been the focus of a successful funding bid and is being implemented to safeguard this species, which was selected as the people's choice in the national flower of Guinea campaign (Couch, Reference Couch, Magassouba, Rokni, Williams and Canteiro2018) involving state school pupils, local communities and authorities. There is little awareness amongst Guinean residents that their country has a unique flora. The national flower of Guinea campaign enabled the introduction of this concept, and a guide for secondary school teachers (Cheek & Magassouba, Reference Cheek, Poveda and Molmou2018) has been produced to engage children and teachers in appreciating and conserving Guinean flora. Raising awareness is written into the conservation action plans to capitalize on these efforts and engage a broader audience, encouraging pride in the Guinean native flora and highlighting the importance of conserving it.

The Guinean national economic and social development plan predicted a median economic growth of 6.5% between 2016 and 2020, with 12.3% occurring because of the revitalization of the mining subsector (OECD, 2017). However, it is not necessary for development to involve destruction of the environment and global extinction of species. Good management based on reliable data and analysis can improve industry practices. Mining projects in Guinea are responsible for mitigating their environmental impact, including the conservation of threatened plant species occurring in the concessions in which they operate. Species new to science have been collected as a result of vegetation surveys conducted in such projects (Goyder, Reference Couch, Molmou and Magassouba2009; Fischer et al., Reference Couch, Molmou, Larridon and Magassouba2011; van der Burgt et al., Reference Magassouba, Camara, Guilavogui, Cheek, Couch and Lopez Poveda2012; Cheek & Williams, Reference Couch2016). In some instances, effective mitigation has been achieved following the discovery of key species during such surveys. One example occurred when botanists found and assessed four threatened species (Stylochaeton pilosus, M. exellii, Raphionacme caerulea and T. hutchinsonii) on a coastal inselberg at an intended new port site for Simfer S.A. in Senguelen. Responding to the risk that these species would be affected significantly by the port construction, Simfer S.A. amended its construction plans to avoid damaging the plants and funded programmes to bank their seeds and develop propagation protocols for them (Couch et al., Reference Couch, Molmou, Camara, Cheek, Merklinger and Davies2014, Reference Couch and Molmou2019a).

Most of the existing conservation efforts in Guinea are focused on mammals, especially the western chimpanzee Pan troglodytes verus (Sugiyama & Soumah, Reference Lebbie1988; Fleury-Brugière & Brugière, Reference Couch, Molmou and Magassouba2010; Humle et al., Reference Couch, Molmou and Magassouba2011). Conservation efforts have also focused on birds, on species threatened by trade, on ecosystem services or on landscape-level protection (e.g. the transboundary Nimba Mountains; Brugière & Kormos, Reference Cheek2008; Correia et al., Reference Couch, Cheek, Haba, Molmou, Williams and Magassouba2010; Nganje et al., Reference Heywood, Shaw, Harvey-Brown and Smith2014). Conservation of endemic and near-endemic plant species has not previously been on the national government agenda. Over 20% of global plant species are estimated to be threatened (Brummitt et al., Reference Cheek and Haba2015; Nic Lughadha et al., Reference Humle, Colin, Laurans and Raballand2020) and one-third of African plant species are at risk of extinction (Stévart et al., Reference Keay and Hepper2019; but see Walker et al., Reference Monteiro, Machado, Martins, Pougy, Verdi and Martinelli2020). Guinea has > 270 threatened species, of which 77 are endemic. Given the person-hours required (c. 1,200 h over 9 months) to write 20 conservation action plans for threatened species, our experience suggests that some endemic species could be treated more effectively using local area action plans addressing multiple species. These could be based on the 22 identified Tropical Important Plant Areas provided that these adequately cover the species’ distribution (Monteiro et al., 2018). Fieldwork has yielded many new data points, which could facilitate an examination of whether most or all of the known/modelled subpopulations of the endemic species in question are encompassed within Tropical Important Plant Areas.

Most of the currently protected areas in Guinea do not overlap with concentrations of threatened plant species (Couch et al., Reference Couch and Molmou2019a). Although the Tropical Important Plant Area framework does not require that all Tropical Important Plant Areas be legally protected (Darbyshire et al., Reference Couch and Molmou2017), in 2019 the government of Guinea committed to incorporating the 22 Tropical Important Plant Areas into the protected area network. Although formal reserve or national park status would be most appropriate for some of the larger Tropical Important Plant Areas, 10 of them are small (0.1–15 km2) and could be better conserved through community protection.

The 20 conservation action plans will be used to target plant conservation and to seek funding, but not only in protected areas. They also have the potential to form the basis of conservation planning and mitigation strategies for the extractive industries in those cases where project footprints intersect with those of the threatened plant species. Currently, seven of the 20 species we assessed occur within mining concessions. As conservation action plans are written for only 20 of the 273 threatened species in Guinea, much research remains to be done. This study demonstrates that whilst developing individual species conservation action plans can be useful for seeking funding for specific species, it is not necessarily the most efficient use of the limited resources available. Broader multi-species conservation action plans or local area conservation action plans based on Tropical Important Plant Areas are potentially more effective means of conservation planning that reduce the timeframe needed for development and thus facilitate more rapid implementation.

In October 2020, a new project was launched to conserve threatened trees in three Tropical Important Plant Areas in coastal Guinea. As part of this project, the Working Group on Tropical Important Plant Areas and Conservation Action Plans is initiating a multi-species national conservation action plan for the 42 tree species known to be threatened. Funding to pilot the incorporation of species conservation action plans in existing management plans for protected areas was obtained in March 2020. Implementation of the current conservation action plans and the formulation of multi-species conservation action plans will assist in updating and modifying the conservation action plan protocol, rendering it a more useful and relevant tool in future conservation planning.

Acknowledgements

This paper is dedicated to Sékou Moussa Keita who passed away during its preparation. This work was funded through a grant from the Global Biodiversity Information Facility, Biodiversity Information for Development programme (reference number AF2015-0042-NAC) ‘Towards a Red Data Book for Guinea’ in collaboration with the Darwin Initiative-funded Tropical Important Plant Areas project (Darwin Project 23-002) and completed with support from Fondation Franklinia. We thank all of those involved in fieldwork in Guinea over the past 10 years who have gathered data, notably Pépé Haba, Gbamon Konomou, Pierre Haba, Fatoumata Fofana Madé, Almamy Diallo, Natalie Konig, Oliver Hooper, Abdoulaye Baldé, Nagnouma Conde, Tokpa Seny Dore, Albert Guilavogui, Boubacar Sow and Saba Rokni; the Kew volunteers Margaret Joachim and Rosemary Lomer who georeferenced herbarium specimens for both projects; Cátia Canteiro and Emma Williams for their work on writing IUCN Red List assessments for Guinean plant species; and the reviewers who provided substantial feedback. This work has been enabled by the Memorandum of Understanding between Royal Botanic Gardens, Kew, and Herbier National de Guinée since 2008.

Author contributions

Writing, compilation: CC, DM; contribution to and revision of conservation action plans: all authors; revision: ENL, XvdB, IL, MC; writing of Biodiversity Information for Development funding proposal: ID, MC.

Conflicts of interest

None.

Ethical standards

This research was carried out in accordance with the Oryx code of conduct.

Footnotes

*

Also at: Department of Biology, Systematic and Evolutionary Botany Lab, Ghent University, Ghent, Belgium

Supplementary material for this article is available at doi.org/10.1017/S0030605322000138

References

African Plant Database (2019) Conservatoire et Jardin Botaniques de la Ville de Genève and South African National Biodiversity Institute, Pretoria (version 3.4.0). ville-ge.ch/musinfo/bd/cjb/africa [accessed 20 August 2019].Google Scholar
Akçakaya, H.R., Bennett, E.L., Brooks, T.M., Grace, M.K., Heath, A., Hedges, S. et al. (2018) Quantifying species recovery and conservation success to develop an IUCN Green List of Species. Conservation Biology, 32, 11281138.CrossRefGoogle ScholarPubMed
Bolam, F.C., Mair, L., Angelico, M., Brooks, T.M., Burgman, M., Hermes, C. et al. (2021) How many bird and mammal extinctions has recent conservation action prevented? Conservation Letters, 14, e12762.CrossRefGoogle Scholar
Brugière, D. & Kormos, R. (2008) Review of the protected area network in Guinea, West Africa, and recommendations for new sites for biodiversity conservation. Biodiversity and Conservation, 18, 847–868.Google Scholar
Brummitt, N.A., Bachman, S.P., Griffiths-Lee, J., Lutz, M., Moat, J.F., Farjon, A. et al. (2015) Green plants in the red: a baseline global assessment for the IUCN sampled Red List Index for plants. PLOS ONE, 10, e0135152.CrossRefGoogle Scholar
Cheek, M. (2013) Marsdenia exellii. In The IUCN Red List of Threatened Species 2013. dx.doi.org/10.2305/IUCN.UK.2013-1.RLTS.T21480972A21481025.en.Google Scholar
Cheek, M. (2017) Habenaria jaegeri. In The IUCN Red List of Threatened Species 2017. dx.doi.org/10.2305/IUCN.UK.2017-2.RLTS.T15368405A15368408.en.Google Scholar
Cheek, M. & Haba, P.M. (2016b) Inversodicraea Engl. resurrected and I. pepehabai sp. nov. (Podostemaceae), a submontane forest species from the Republic of Guinea. Kew Bulletin, 71, 55.CrossRefGoogle Scholar
Cheek, M. & Magassouba, S. (2018) L'Importance de la Conservation des Plantes en Guinée. Guide a l'Intention des Enseignants du Secondaires. Solopress, Southend-on-Sea, UK.Google Scholar
Cheek, M. & Williams, T. (2016) Psychotria samoritourei (Rubiaceae), a new liana species from Loma-Man in upper Guinea, West Africa. Kew Bulletin, 71, 19.CrossRefGoogle Scholar
Cheek, M., Magassouba, S., Howes, M.R., Dore, T.S., Doumbouya, S., Molmou, D. et al. (2018) Kindia (Pavetteae, Rubiaceae), a new cliff-dwelling genus with chemically profiled colleter exudate from Mt Gangan, Republic of Guinea. PeerJ, 6, e4666.CrossRefGoogle ScholarPubMed
Cheek, M., Poveda, L.L. & Molmou, D. (2015) Tarenna hutchinsonii (Rubiaceae) redelimited, and T. agnata described from W. Africa. Kew Bulletin, 70, 12.CrossRefGoogle Scholar
Correia, M., Diabaté, M., Beavogui, P., Guilavogui, K., Lamanda, N. & de Foresta, H. (2010) Conserving forest tree diversity in Guinée forestière (Guinea, West Africa): the role of coffee-based agroforests. Biodiversity and Conservation, 19, 1725–1747.CrossRefGoogle Scholar
Couch, C., Molmou, D., Camara, B., Cheek, M., Merklinger, F. Davies, L. et al. (2014) Conservation of Threatened Guinean Inselberg Species. Abstracts of the XXth AETFAT Congress, South Africa, 2014. Scripta Botanica Belgica, 52, 96.Google Scholar
Couch, C. (2018) Guinea: The Campaign for a National Flower. kew.org/read-and-watch/guinea-the-campaign-national-flower [accessed 20 August 2019].Google Scholar
Couch, C. (ed.) (2019) Protocole pour les Plans d'Actions de Conservation. herbierguinee.org/uploads/2/6/3/0/26303479/protocole_des_pacs.pdf [accessed 20 July 2022].Google Scholar
Couch, C., Cheek, M., Haba, P., Molmou, D., Williams, J., Magassouba, S. et al. (2019a) Threatened Habitats and Tropical Important Plant Areas of Guinea, West Africa. Solopress, Southend-on-Sea, UK.Google Scholar
Couch, C., Magassouba, S., Rokni, S., Williams, E. & Canteiro, C. (2019b) Threatened plants species of Guinea-Conakry: a preliminary checklist. Preprint publication. PeerJ Preprints, doi.org/10.7287/peerj.preprints.3451v4.Google Scholar
Couch, C. & Molmou, D. (2019a) Conservation Action Plan (CAP): Habenaria jaegeri. dx.doi.org/10.13140/RG.2.2.11630.56644.Google Scholar
Couch, C. & Molmou, D. (2019b) Conservation Action Plan (CAP): Inversodicraea pepehabai. dx.doi.org/10.13140/RG.2.2.25052.33925.Google Scholar
Couch, C. & Molmou, D. (2019c) Conservation Action Plan (CAP): Pitcairnia feliciana. dx.doi.org/10.13140/RG.2.2.21696.89609.Google Scholar
Couch, C., Molmou, D., Larridon, I. & Magassouba, S. (2019c) Conservation Action Plan (CAP): Scleria guineensis. doi.org/10.13140/RG.2.2.23374.61767.Google Scholar
Couch, C., Molmou, D. & Magassouba, S. (2019d) Conservation Action Plan (CAP): Coleus (Plectranthus) linearifolius. dx.doi.org/10.13140/RG.2.2.35118.66880/1.Google Scholar
Couch, C., Molmou, D. & Magassouba, S. (2019e) Conservation Action Plan (CAP): Diospyros feliciana. dx.doi.org/10.13140/RG.2.2.15824.87047.Google Scholar
Couch, C., Molmou, D. & Magassouba, S. (2019f) Conservation Action Plan (CAP): Keetia susu. dx.doi.org/10.13140/RG.2.2.18341.45280.Google Scholar
Couch, C., Molmou, D. & Magassouba, S. (2019g) Conservation Action Plan (CAP): Marsdenia exellii. dx.doi.org/10.13140/RG.2.2.28407.78244.Google Scholar
Couch, C., Molmou, D. & Magassouba, S. (2019h) Conservation Action Plan (CAP): Pterocarpus erinaceus. dx.doi.org/10.13140/RG.2.2.30085.50401.Google Scholar
Couch, C., Molmou, D. & Magassouba, S. (2019i) Conservation Action Plan (CAP): Stylochaeton pilosus. dx.doi.org/10.13140/RG.2.2.36796.39049.Google Scholar
Couch, C., Molmou, D. & Magassouba, S. (2019j) Conservation Action Plan (CAP): Tarenna hutchinsonii. dx.doi.org/10.13140/RG.2.2.20097.81766.Google Scholar
Couch, C., Molmou, D. & Magassouba, S. (2019k) Conservation Action Plan (CAP): Tieghemella heckelii. dx.doi.org/10.13140/RG.2.2.33519.59047.Google Scholar
Couch, C., Molmou, D. & Magassouba, S. (2019l) Conservation Action Plan (CAP): Vepris felicis. dx.doi.org/10.13140/RG.2.2.18420.09606.Google Scholar
Couch, C., Molmou, D. & Magassouba, S. (2019m) Conservation Action Plan (CAP): Vernonia djalonensis. dx.doi.org/10.13140/RG.2.2.15064.65289.Google Scholar
Couch, C., Molmou, D. & Magassouba, S. (2019n) Conservation Action Plan (CAP): Xysmalobium samoritourei. dx.doi.org/ 10.13140/RG.2.2.28486.42561.Google Scholar
Couch, C., Molmou, D. & van der Burgt, X.M. (2019o) Conservation Action Plan (CAP): Talbotiella cheekii. dx.doi.org/ 10.13140/RG.2.2.30164.14728.Google Scholar
Couch, C., Molmou, D., van der Burgt, X.M. & Magassouba, S. (2019p) Conservation Action Plan (CAP): Eriosema triformum. dx.doi.org/10.13140/RG.2.2.35957.52965/1.Google Scholar
Darbyshire, I., Anderson, S., Asatryan, A., Byfield, A., Cheek, M., Clubbe, C. et al. (2017) Important plant areas: revised selection criteria for a global approach to plant conservation. Biodiversity and Conservation, 26, 17671800.CrossRefGoogle Scholar
Fischer, E., Darbyshire, I. & Cheek, M. (2011) Striga magnibracteata (Orobanchaceae) a new species from Guinée and Mali. Kew Bulletin, 66, 441445.CrossRefGoogle Scholar
Fleury-Brugière, M.C. & Brugière, D. (2010) High population density of Pan troglodytes verus in the Haut Niger National Park, Republic of Guinea: implications for local and regional conservation. International Journal of Primatology, 31, 383392.CrossRefGoogle Scholar
GBIF (Global Biodiversity Information Facility) (2019) gbif.org [accessed 21 October 2019].Google Scholar
Goyder, D.J. (2009) Xysmalobium samoritourei (Apocynaceae: Asclepiadoideae), a new species from the Guinea highlands of West Africa. Kew Bulletin, 63, 473475.CrossRefGoogle Scholar
Grace, M.K., Akçakaya, H.R., Bennett, E.L., Brooks, T.M., Heath, A., Hedges, S. et al. (2021) Testing a global standard for quantifying species recovery and assessing conservation impact. Conservation Biology, 35, 18331849.CrossRefGoogle ScholarPubMed
Guinean Ministry of Mines and Geology (2016) Bauxite: becoming a world leading producer. mines.gov.gn/en/resources/bauxite [accessed 21 October 2019].Google Scholar
Heywood, V., Shaw, K., Harvey-Brown, Y. & Smith, P. (eds) (2018) BGCI and IABG's Species Recovery Manual. Botanic Gardens Conservation International, Richmond, UK.Google Scholar
Humle, T., Colin, C., Laurans, M. & Raballand, E. (2011) Group release of sanctuary chimpanzees (Pan troglodytes) in the Haut Niger National Park, Guinea, West Africa: ranging patterns and lessons so far. International Journal of Primatology, 32, 456473.CrossRefGoogle Scholar
International Plant Names Index (2019) International Plant Names Index. The Royal Botanic Gardens, Kew, Richmond, UK, Harvard University Herbaria & Libraries, Cambridge, USA, and Australian National Botanic Gardens, Canberra, Australia. ipni.org [accessed 29 July 2021].Google Scholar
IUCN (2012a) Threat Classification Scheme (version 3.2). iucnredlist.org/resources/threat-classification-scheme [accessed 2 December 2021].Google Scholar
IUCN (2012b) IUCN Red List Categories and Criteria. Version 3.1. 2nd edition. IUCN, Gland, Switzerland and Cambridge, UK.Google Scholar
IUCN (2021a) Green Status of Species Guidelines and Assessment Materials. iucnredlist.org/resources/green-status-assessment-materials [accessed 10 June 2021].Google Scholar
IUCN (2021b) Table 1a. Number of species evaluated in relation to the overall number of described species, and numbers of threatened species by major groups of organisms. Updated 25 March 2021. iucnredlist.org/resources/summary-statistics [accessed 10 June 2021].Google Scholar
IUCN (2021c) The IUCN Red List of Threatened Species 2021-3. iucnredlist.org [accessed 10 June 2021].Google Scholar
JNCC UK (2010a) Priority species pages: Aceras anthropophorum (L.) W.T. Aiton. Version 2. archive.jncc.gov.uk/_speciespages/2470.pdf [accessed 1 May 2018].Google Scholar
JNCC UK (2010b) Priority species pages: Astragalus alpinus L. Version 2 updated. archive.jncc.gov.uk/_speciespages/2068.pdf [accessed 1 May 2018].Google Scholar
Keay, R.W.J. & Hepper, N. (eds) (1954–1972) Flora of West Tropical Africa. Royal Botanic Gardens, Kew. Crown Agents, London, UK.Google Scholar
Lebbie, A.R. (2001) Guinean Montane Forests (AT0114). WWF Terrestrial Ecoregions. worldwildlife.org/wildworld/profiles/terrestrial/at/at0114_full.html [accessed 13 December 2019].Google Scholar
Lisowski, S. (2009) Flore (Angiospermes) de la République de Guinée. Scripta Botanica Belgica, 41, 1–517.Google Scholar
Magassouba, S., Camara, B., Guilavogui, K., Cheek, M., Couch, C., Lopez Poveda, L. et al. (2014) Hunting threatened taxa of Guinea. In Abstracts of the XXth AETFAT Congress, South Africa, 2014. Scripta Botanica Belgica, 52, 255.Google Scholar
Molmou, D. & Couch, C. (2019a) Conservation Action Plan (CAP): Acalypha guineensis. dx.doi.org/10.13140/RG.2.2.34363.36648.Google Scholar
Molmou, D. & Couch, C. (2019b) Conservation Action Plan (CAP): Anisotes guineensis. dx.doi.org/10.13140/RG.2.2.25974.75845.Google Scholar
Monteiro, L., Machado, N., Martins, E., Pougy, N., Verdi, M., Martinelli, G. et al. (2018) Conservation priorities for the threatened flora of mountaintop grasslands in Brazil. Flora, 238, 234243.CrossRefGoogle Scholar
Nganje, M., Lebbie, A., Sambollah, R. & Waugh, J. (2014) Mid-Term Performance Evaluation of the Sustainable and Thriving Environments for West Africa Regional Development (STEWARD III) Project. dx.doi.org/10.13140/RG.2.1.1243.6966.Google Scholar
Nic Lughadha, E., Bachman, S.P., Leão, T.C., Forest, F., Halley, J.M., Moat, J. et al. (2020) Extinction risk and threats to plants and fungi. Plants, People, Planet, 2, 389408.CrossRefGoogle Scholar
OECD (2017) Guinea African Economic Outlook 2017. africaneconomicoutlook.org/guinea [accessed 15 December 2020].Google Scholar
Panjabi, S., Neely, B. & Lyon, P. (2011) Rare Plant Conservation Action Plan: Big Gypsum Valley and Dry Creek Basin, Colorado. Unpublished report. The Nature Conservancy and the Colorado Natural Heritage Program for the National Fish and Wildlife Foundation, Fort Collins, USA.Google Scholar
Phillipson, P., Hooper, O., Haba, P., Cheek, M. & Paton, A. (2019) Three species of Coleus (Lamiaceae) from the Guinean highlands: a new species, a new combination and clarification of Coleus splendidus. Kew Bulletin, 74, 24.CrossRefGoogle Scholar
Plants of the World Online (2022) Plants of the World Online. Royal Botanic Gardens, Kew, Richmond, UK. powo.science.kew.org [accessed October 2022].Google Scholar
Royal Botanic Gardens, Kew (2016) The State of the Worlds Plants Report – 2016. Royal Botanic Gardens, Kew, Richmond, UK.Google Scholar
Sayer, J.A., Harcourt, C.S. & Collins, N.M. (1992) The Conservation Atlas of Tropical Forests: Africa. IUCN and Simon & Schuster, Cambridge, UK.CrossRefGoogle Scholar
Sengupta, D. (ed.) (2019) Bauxite export by Guinea estimated to grow 13% YoY in 2019; China to remain the top importer. AlCircle, 18 March 2019. alcircle.com/news/bauxite-export-by-guinea-estimated-to-grow-13-yoy-in-2019-china-to-remain-the-top-importer-44444 [accessed 22 August 2019].Google Scholar
Stévart, T., Dauby, G., Lowry, P.P. II, Blach-Overgaard, A., Droissart, V., Harris, D.J. et al. (2019) A third of the tropical African flora is potentially threatened with extinction. Science Advances, 5, 11.CrossRefGoogle ScholarPubMed
Sugiyama, Y. & Soumah, A.G. (1988) Preliminary survey of the distribution and population of chimpanzees in the Republic of Guinea. Primates, 29, 569574.CrossRefGoogle Scholar
The Nature Conservancy (2007) Conservation Action Planning Handbook: Developing Strategies, Taking Action and Measuring Success at Any Scale. The Nature Conservancy, Arlington, USA.Google Scholar
van der Burgt, X.M., Couch, C. & Molmou, D. (2019a) Conservation Action Plan (CAP): Cailliella praerupticola. dx.doi.org/10.13140/RG.2.2.19180.31364.Google Scholar
van der Burgt, X.M., Haba, P.K., Haba, P.M. & Goman, A.S. (2012) Eriosema triformum (Leguminosae: Papilionoideae), a new unifoliolate species from Guinea, West Africa. Kew Bulletin, 67, 263271.CrossRefGoogle Scholar
van der Burgt, X.M., Molmou, D., Diallo, A., Konomou, G., Haba, P.M. & Magassouba, S., (2018) Talbotiella cheekii (Leguminosae: Detarioideae), a new tree species from Guinea. Kew Bulletin, 73, 26.CrossRefGoogle Scholar
van der Burgt, X.M., Konomou, G., Haba, P.M. & Magassouba, S. (2019b) Gladiolus mariae (Iridaceae), a new species of fire-free shrubland in the Kounounkan Massif, Guinea. Willdenowia, 49, 117126.CrossRefGoogle Scholar
Walker, B.E., Leão, T.C., Bachman, S.P., Bolam, F.C. & Nic Lughadha, E. (2020) Caution needed when predicting species threat status for conservation prioritization on a global scale. Frontiers in Plant Science, 11, 520.CrossRefGoogle ScholarPubMed
Way, M. & Gold, K. (2014) Assessing a Population for Seed Collection. Millennium Seed Bank Partnership Technical Information Sheet 02. brahmsonline.kew.org/Content/Projects/msbp/resources/Training/02-Assessing-population.pdf [accessed 2 September 2019].Google Scholar
Xanthos, M., Konomou, G., Haba, P.M. & van der Burgt, X.M. (2020) Trichanthecium tenerium (Poaceae: Panicoideae), a new species from Guinea-Conakry. Kew Bulletin, 75, 11.CrossRefGoogle Scholar
Figure 0

Table 1 List of species chosen for conservation action plans, with the IUCN Red List status (IUCN, 2021c), growth form and collection data in Guinea resulting from recent fieldwork. See supplementary materials for links to individual conservation action plans.

Figure 1

Fig. 1 The known distribution of four endemic Guinean species: (a) Anisotes guineensis, (b) Talbotiella cheekii, (c) Diospyros feliciana and (d) Eriosema triformum.

Figure 2

Fig. 2 Per cent of the 20 species for which we prepared conservation action plans (Table 1) subject to each of eight threat types of the IUCN Threat Classification Scheme (IUCN, 2012a).

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