Botanic gardens have been encouraged to focus their efforts on the regional flora where they are located and to adopt measures for species conservation both in the natural environment (in situ) and in cultivation (ex situ; Botanical Garden Conservation International, 2014; Costa et al., Reference Costa, Maunder, Pereira and Peixoto2016). The role of botanic gardens in these fields is well known, although much remains to be done, especially in tropical countries with a high diversity of environments and species, such as Brazil (Silveira et al., Reference Silveira, Teixido, Zanetti, Pádua, Andrade and Costa2018).
Microendemic plants are of great interest for conservation because of their often reduced, isolated and threatened populations. Conservation actions for microendemic plants include research on artificial propagation, genetic diversity, ecophysiology and pollination, monitoring, threat mitigation, reintroduction and ex situ conservation (Zhang et al., Reference Zhang, Luo and Chen2014; Kraaij et al., Reference Kraaij, Baard and Crain2016; Médail & Baumel, Reference Médail and Baumel2018).
Some microendemic species of Monimiaceae have been objects of study and conservation actions, focused mainly on fieldwork, with some recently rediscovered species (Mollinedia stenophylla Perkins and Mollinedia myriantha Perkins; Lírio et al., Reference Lírio, Freitas, Negrão, Martinelli and Peixoto2018a, Lírio et al., Reference Lírio, Freitas, Pauli, Rosa, Prieto, Negrão and Peixotoin press). Another project that is still ongoing, led by EJdL, aims to bring together the local community, germination protocols and fieldwork to conserve two threatened Monimiaceae, Mollinedia dolichotricha Lírio & Peixoto and Mollinedia ruschii Lírio & Peixoto, with the latter being microendemic (Lírio & Peixoto, Reference Lírio and Peixoto2015; Lírio et al., Reference Lírio, Negrão, Sano and Peixoto2021).
Grazielanthus Peixoto & Per.-Moura (Monimiaceae, Laurales) is a monotypic genus and has unexpected characteristics for a Neotropical Monimiaceae: a shrub or lianoid habit, pistillate flowers without a circumcise apex and numerous fruitlets closed in the fruiting receptacle until maturation, when it opens with irregular slits. This unique set of characteristics probably reflects the evolutionary distinctiveness of this taxon (Peixoto & Pereira-Moura, Reference Peixoto and Pereira-Moura2008; Lírio et al., Reference Lírio, Peixoto, Negrão, Amorim, Braga, Avancini, Martinelli, Martins, Moraes, Loyola and Amaro2018b).
Grazielanthus arkeocarpus Peixoto & Per.-Moura is a microendemic species from Rio de Janeiro State, characterized by having an average height of 2–10 m, with simple, opposite and serrated leaves. The staminate flowers are yellow and organized in triflorous inflorescences, with an urceolate receptacle, four tepals and 35–37 rounded stamens opening through slits. The pistillate flowers are solitary and have 35–37 free carpels. The fruiting receptacle has persistent tepals at the apex and is yellowish-green externally and yellow internally. It remains closed until the fruitlets mature, when it then dehisces irregularly. The fruitlets with their fleshy pericarp are probably adapted to zoochoric dispersal (Plate 1a–g).
With the aid of the National Centre for Flora Conservation (the Brazilian IUCN Red List Authority for plants) we categorized the species as Critically Endangered on the basis of criteria B2ab(ii,iii); C2a(ii); D: area of occupancy estimated to be 4 km2 (B2), known to exist at only a single location (a), with continuing decline (b) in area of occupancy (ii), area, extent and/or quality of habitat (iii); population size estimated to be c. 32 mature individuals and continuing decline inferred, in numbers of mature individuals (C2) with 100% of mature individuals in one subpopulation (ii); population size estimated to be c. 80 individuals, of which c. 40% are mature and reproductive (D) (Lírio et al., Reference Lírio, Peixoto, Negrão, Amorim, Braga, Avancini, Martinelli, Martins, Moraes, Loyola and Amaro2018b). This recommendation will be included on the IUCN Red List in due course.
Grazielanthus arkeocarpus inhabits a flood prone alluvial forest in the Atlantic Forest, in the Poço das Antas Biological Reserve, a fully protected area (IUCN category Ia) created in 1974 in Silva Jardim County (Fig. 1). Alluvial forests occupy c. 894 ha (c. 18%) of the Biological Reserve (Lima et al., Reference Lima, Pessoa, Guedes-Bruni, Moraes, Granzotto, Iwamoto and Cícero2006). The c. 4,856 ha Biological Reserve is home to several threatened species, including the Endangered golden lion tamarin Leontopithecus rosalia, its flagship species.
Actions for the conservation of the golden lion tamarin, such as reforestation, were started in 1993 by the Rio de Janeiro Botanic Garden and continued by the Golden Lion Tamarin Association and other partners. These actions benefitted the population of G. arkeocarpus by minimizing the risk of forest fires in its area of occupancy. Guided by the Global Strategy for Plant Conservation (CBD, 2010) and the Botanic Garden Conservation International recommendations (BGCI, 2014), we developed actions for the conservation of G. arkeocarpus that involved population monitoring, research, ex situ conservation and the expansion of the in situ population.
We began monitoring in 2013 with the marking of individual plants, to investigate their phenology, especially the opening of the receptacles and fruitlet release, and for subsequent collection of seeds. We developed this work in collaboration with researchers, technicians, field assistants and students from the Biological Reserve and the Rio de Janeiro Botanic Garden. The process of exchanging knowledge regarding seedling production was key to consolidating commitment to the conservation of rare and endemic plant species in the region, where some of the team members live. We then began ongoing research that included studies on genetic diversity, genome size estimation, morphology, phylogenetics and seed germination under controlled conditions.
In 2014 we began our first attempt to cultivate G. arkeocarpus outside its natural area. We planted six seedlings in an arboretum as part of the Brazilian species conservation initiative developed by the Rio de Janeiro Botanic Garden (Fig. 1). These seedlings were produced in the Biological Reserve nursery and brought to the Botanic Garden nursery, where they underwent quarantine before planting. Only one individual survived, and since 2017 it has bloomed annually. This staminate specimen suggests that species can be successfully cultivated ex situ. In October 2017 we planted two new seedlings in the same plot from a new batch of seeds, but they did not survive. The seedlings of G. arkeocarpus that we planted in 2021 came from yet another batch of seeds as we continue to attempt to cultivate both staminate and pistillate plants in the Botanic Garden.
In situ conservation efforts involved the expansion of the area of occupancy of the species. During May–June 2019 we collected seeds that we planted immediately in plastic bags and kept in the Biological Reserve nursery for 8 months until the seedlings reached a minimum height of 20 cm. In February 2020, during the rainy season, we planted 84 seedlings in an area of the Biological Reserve c. 1 km from the original location of the species but in similar habitat. The current survival rate in the field is 56%, with a mean height of 52 cm for the 47 surviving seedlings (range 24–96 cm). We continue to monitor these seedlings, seeking information on the beginning of the reproductive period of both staminate and pistillate individuals. As reported previously (Portal ICMBio, 2020), the success of this planting is demonstrated by the health of the developing plants, which are already fully established. This also indicates the species could be used for restoration projects in the Biological Reserve (Plate 1h,i).
To expand these in situ and ex situ conservation actions, we continue to carry out seed collection and seedling production in the Biological Reserve nursery. We have sent G. arkeocarpus seeds and seedlings to two other living plant collections: the University of São Paulo in São Paulo County, São Paulo State, at c. 750 m altitude, where the species is already part of the collection; and the Rio de Janeiro Federal Rural University Botanic Garden, at a low altitude (27 m) in Seropédica County, Rio de Janeiro State, where planting will take place in 2023.
The development of conservation actions for the species will continue. The goals of the in situ and ex situ cultivation are to minimize the risks of the extinction of this species and to facilitate future research that will fill in gaps in our current knowledge of this microendemic species.
Microendemic species are best conserved through integrated in situ and ex situ conservation (BGCI, 2014; Costa et al., Reference Costa, Maunder, Pereira and Peixoto2016), and increasing local commitment to conservation is essential (Crain et al., Reference Crain, Sánchez-Cuervo, White and Steinberg2015). The actions we carried out for G. arkeocarpus demonstrated the importance of persistence and local community involvement in achieving meaningful results. We hope this research will inspire other initiatives focused on microendemic plants in Brazil and other countries, help support the management of in situ protected areas where such species occur, and expand the representation of rare, microendemic and threatened species in ex situ living plant collections.
Acknowledgements
We thank the Biological Reserve and Botanic Garden staff; Adilson Pintor, Jonas A. Dias, Mário R. Silva and Valmir F. Santos for their assistance in planting in the field and daily seedling care at the nursery; Vanderlei Rodinsky, who is responsible for the Botanic Garden nursery; the living collections coordinators Claudio N. Fraga and Marcus N. Coelho; Maurício Porto who prepared the map figure; and Danilo A. Zavatin, Michel Ribeiro, André L.P. Leite, Rickson G.S. Farias and Walace B. Silva for their help with fieldwork. This research did not receive specific funding from any funding agency or the commercial or non-profit sectors.
Author contributions
Collection, identification, marking of specimens in the field and risk assessment: ALP, EJdL; monitoring of phenophases, collection of seeds and monitoring the development of seedlings in situ: GLP; monitoring ex situ: THMdA, DRG; data management for the ex situ collection: THMdA; plate preparation: DRG; writing: all authors.
Conflicts of interest
None.
Ethical standards
This research abided by the Oryx guidelines on ethical standards.