ArticlePDF Available

Abstract and Figures

Vismia conduplicata, a new species of Hypericaceae from Mato Grosso state, Brazil, is described and illustrated. It is associated to "campos de murundus", a kind of Cerrado physiognomy with woody plants growing on earth mounds, in a grassland matrix. The species was included in Vismia sect. Trianthera, based on the number of stamens per stamen fascicle and the number of ovules per locule. A comparison with the morphologically similar species Vismia micrantha is also provided.
Content may be subject to copyright.
Phytotaxa 338 (1): 125–129
http://www.mapress.com/j/pt/
Copyright © 2018 Magnolia Press Article PHYTOTAXA
ISSN 1179-3155 (print edition)
ISSN 1179-3163 (online edition)
Accepted by Ana Giulietti Harley: 5 Jan. 2018; published: 9 Feb. 2018
https://doi.org/10.11646/phytotaxa.338.1.11
125
Vismia conduplicata (Hypericaceae), a new species from Mato Grosso, Brazil
MILENA VENTRICHI MARTINS1,*, GUSTAVO HIROAKI SHIMIZU1, VOLKER BITTRICH2 & MARIA DO
CARMO ESTANISLAU DO AMARAL1
1Departamento de Biologia Vegetal, Instituto de Biologia, Universidade Estadual de Campinas, Rua Monteiro Lobato 255, 13083-862,
Campinas, SP, Brazil.
2Rua Dr. Mario de Nucci 500, 13083-290, Campinas, SP, Brazil.
*Author for correspondence: milory@gmail.com
Abstract
Vismia conduplicata, a new species of Hypericaceae from Mato Grosso state, Brazil, is described and illustrated. It is associ-
ated to “campos de murundus”, a kind of Cerrado physiognomy with woody plants growing on earth mounds, in a grassland
matrix. The species was included in Vismia sect. Trianthera, based on the number of stamens per stamen fascicle and the
number of ovules per locule. A comparison with the morphologically similar species Vismia micrantha is also provided.
Key words: clusioid clade, flora of Brazil, Malpighiales, taxonomy
Resumo
Vismia conduplicata, uma nova espécie de Hypericaceae do estado do Mato Grosso, Brasil, é descrita e ilustrada. Ela é as-
sociada aos campos de murundus, um tipo de fisionomia do Cerrado com plantas lenhosas crescendo sobre montes de terra,
numa matriz campestre. A espécie foi incluída em Vismia sect. Trianthera, com base no número de estames por fascículo de
estames e no número de óvulos por lóculo. Uma comparação com a espécie morfologicamente similar Vismia micrantha é
também fornecida.
Palavras-chave: clado clusioide, flora do Brasil, Malpighiales, taxonomia
Introduction
Vismia Vandelli (1788: 51) is a Neotropical genus of Hypericaceae with 50 to 65 species (Robson 1998, Stevens
2007, Gustafsson 2017). Reichardt (1878) has recognized three sections, based on number of stamens per fascicle and
number of ovules per locule: Vismia sect. Trianthera Reichardt (1878: 197), with three stamens per fascicle and one
or two ovules per locule; Vismia sect. Stictopetalum Reichardt (1878: 198), with five stamens per fascicle and many
ovules per locule; and Vismia sect. Vismia, with many stamens per fascicle and many ovules per locule (Reichardt
1878). Currently, 29 species are recognized in Brazil, of which nine are endemic to the country. For the state of Mato
Grosso nine species of Vismia are cited (Flora do Brasil 2020).
The species of Vismia are trees, treelets, or shrubs, with a characteristic orange to red exudate, and usually with
trichomes on branches, leaves, inflorescence and/or floral structures. The leaves are nearly always opposite and usually
show black dots on the abaxial surface. Most species have a terminal, branched thyrsoid inflorescence, rarely axillary
or cauliflorous, with pentamerous flowers, homostylous or heterostylous, sepals and petals frequently with dots or
canals (vittae), petals conspicuously hairy on the adaxial surface; the androecium is composed of five fascicles, with
three to numerous stamens each, alternating with short hairy staminodes (nectaries). The coriaceous berries are mainly
globose or ovoid, often with persistent sepals, styles, stigmas, and sometimes stamen fascicles (Ewan 1962, Robson
1998, Stevens 2007).
After analyzing several herbarium collections for the ongoing taxonomic studies of the Brazilian species of
Vismia, some specimens from Mato Grosso state, western Brazil, called our attention, owing to their conduplicate
MARTINS ET AL.
126 Phytotaxa 338 (1) © 2018 Magnolia Press
and narrowly elliptic leaves, variable phyllotaxis (opposite, whorled or alternate, sometimes on the same branch),
and stamen fascicles with three stamens each. They were previously identified as V. micrantha Saint-Hilaire (1828:
327) or V. cf. cavalcantei Berg (1970: 1), but the combined set of referred traits makes clear that it is a species new to
science.
Material and Methods
Herbarium acronyms cited follow Thiers (2017). For two of the three known collections, without precise coordinates,
an approximation was made using Google Maps and municipality coordinates. These data were used to produce the
distribution map, using ArcGIS, and to perform the conservation assessment, using GeoCAT (Bachman et al. 2011).
Taxonomic treatment
Vismia conduplicata M.V.Martins & G.H.Shimizu, sp. nov. (Fig. 1)
Type:—BRAZIL. Mato Grosso: Luciara, Estrada para a Mata do Coco, ca. 16 km N de Luciara, Fazenda Três Pontas do Araguaia,
11°07’21,9’’S, 50°44’17,5’’W, 140 m, 19 March 1997, fl., fr., V.C. Souza, J.P. Souza, A.R. Duarte & F.F. Mazine 14492 (holotype:
ESA! [mounted on two sheets with the same herbarium accession number - ESA43012]; isotypes: BHCB [photo!], FUEL!, INPA!,
MBM!, PEL, SPSF [photo!], UEC!).
Vismia conduplicata can be recognized by the combination of variable phyllotaxis (opposite, whorled or alternate, sometimes on the same
branch), conduplicate and narrowly elliptic leaves, stamen fascicles with three stamens each, two black glands between the thecae,
and sepals ascendant to patent on mature berries.
Shrubs, 1.5–3 m tall; branches brownish, sometimes peeling, glabrous; exudate not reported by collectors. Leaves
petiolate, opposite or in 3-merous whorls (rarely in 4-merous whorls or alternate); petiole 0.5–1 cm long; leaf blades
3.5–9.4 × 0.5–1.8 cm, chartaceous to subcoriaceous, narrowly elliptic, conduplicate, apex and base acute, margin
entire (sometimes crenulate toward the apex), adaxial surface dark brown in sicco, midrib impressed, secondary veins
prominent, glabrous or glabrescent (midrib sometimes with stellate trichomes), abaxial surface light brown, midrib
and secondary veins prominent, glabrous or glabrescent; venation brochidodromous, secondary veins 18–28 pairs;
black dots present on both surfaces. Inflorescence terminal, thyrsoid, up to 25 flowers, rachis 1–2 cm long, glabrous;
flower buds ca. 2 × 1 mm, ovoid to ellipsoid. Flowers apparently homostylous, pedicel 2–5 mm long, sometimes with
black dots; sepals 5, slightly unequal, ca. 3 × 1 mm, elliptic, apex acute, base truncate, margin sometimes denticulate
at the apex, surface glabrous, four blackish canals (vittae) on both surfaces, more evident on the inner one; corolla
campanulate, petals 5, 5–6 × 2 mm, elliptic, apex acute, base truncate, lanose on inner surface, black dots on upper
half; stamen fascicles 5, 3–5 mm long, each one with 3 stamens, filaments connate except for the apical portion, hirsute
mainly on central portion, free portion 1.3–1.6 mm long, anthers ca. 0.2 mm long, with two black glands between the
thecae; staminodes ca. 1 mm long, deltoid, lanose; ovary ca. 2 mm long, ovate, 5-locular, 1-ovulate per locule, glabrous
(sometimes apex with few trichomes), surface with black dots, styles 2.8–3.1 mm long, glabrous, with black dots,
stigmas disk-shaped. Berries 5–7 × 6 mm, ovate to spherical, coal black in sicco; sepals, stamen fascicles, staminodes,
and styles persistent; sepals ascendant to patent on mature berries. Seeds 1 per locule, 2.5–4 × 1–1.5 mm, oblong to
elliptical, curved.
Additional specimens examined (paratypes):—BRAZIL. Mato Grosso: Lucas do Rio Verde, campo de
murundus, 10 June 1996, bud, E.A. Silveira 22 (UFMT). Nova Xavantina, Fazenda Brejo Azul, approx. 10 km S of
Xavantina, 14°44’S, 52°20’W, 14 January 1977, fl., fr., J.A. Ratter et al. 4128 (CPAP, E, K, MO, NY, UB, UEC).
Tapurah, estrada MT-010, cerca de 5 km do entroncamento com MT-338, 12°49’S, 56°26’W, savana arborizada com
trechos alagáveis, 12 June 1997, fr., V.C. Souza et al. 17812 (ESA, MBM, PEL, RB, SPF, UEC).
Etymology:—The specific epithet refers to the conduplicate (lengthwise folded upwards) leaves.
Distribution, habitat, and conservation:Vismia conduplicata is so far only known from four localities within
Mato Grosso state, in the Central-West region of Brazil (Fig. 2). Two of them, Lucas do Rio Verde and Tapurah, are
neighbouring municipalities, in the central portion of the state. On the other hand, Luciara and Nova Xavantina are
almost 1000 km distant to them, the former on the border with the state of Tocantins and the latter more towards
the south. The species occurs in one of the vegetation physiognomies of the Brazilian Cerrado called “campo de
VISMIA CONDUPLICATA (HYPERICACEAE) Phytotaxa 338 (1) © 2018 Magnolia Press 127
FIGURE 1. Vismia conduplicata. A. Branch with flower buds. B. Abaxial leaf surface. C. Detail of the abaxial leaf surface, showing black
dots. D. Flower bud. E. Open flower in lateral view. F. Sepal in outer view. G. Petal in outer (left) and inner (right) view. H. Dissected
flower, showing sepals, petals, stamen fascicles, staminodes, and gynoecium. I. Stamen fascicle in inner (left) and outer (right) view. J.
Young stamen showing two black glands between thecae. K. Fruit. AC. E.A. Silveira 22. D–J. V.C. Souza et al. 14492. K. V.C. Souza et
al. 17812. Drawn by Klei Sousa.
MARTINS ET AL.
128 Phytotaxa 338 (1) © 2018 Magnolia Press
murundus” (mound fields) (e.g. Oliveira-Filho 1992, Marimon et al. 2012) or “parque de Cerrado” (Ribeiro & Walter
2008), which consists basically of earth mounds covered by Cerrado typical woody plants in a grassland matrix usually
hit by seasonal floodings (Oliveira-Filho 1992, Silva 2010, Marimon et al. 2015).
Although we have used the GeoCAT tool to assess the conservation status, we considered more cautious to assign
it as DD (Data Deficient) at the moment, based on the few information presently available. New collection efforts may
help to designate a better supported conservation status.
Phenology:—Specimens were collected with flower buds in June, with flowers in January, March and with fruits
in January, March and June.
Comments:—Although there are few specimens available, apparently the flowers are homostylous, due to the
similar lengths of the stamen fascicles in all specimens observed.
The new species is placed in Vismia sect. Trianthera due to the stamen fascicles composed of three stamens
and the 1-ovulate locules. It can be distinguished from Vismia micrantha, which also belongs to this section, by
the narrowly elliptic and conduplicate leaves (vs. elliptic to lanceolate and usually flat in V. micrantha), variable
phyllotaxis (alternate, opposite or whorled), sometimes on the same branch (vs. opposite), sepals with blackish canals
present (vs. absent), deltoid staminodes (vs. rectangular), and glabrous styles (vs. trichomes present). Moreover, Vismia
conduplicata occurs in the “campos de murundus” of Mato Grosso state, whereas V. micrantha is found in the forest
formations of Southeastern Brazil (Flora do Brasil 2020).
FIGURE 2. Geographical distribution map of Vismia conduplicata.
Acknowledgements
MVM and GHS thank CAPES/PROTAX (001/2015) for financial support and scholarships. MCEA thanks for the
grant 2016/50382-5, São Paulo Research Foundation (FAPESP) and a productivity grant from CNPq (312479/2013-1).
We are grateful to the curators of the herbaria consulted, to Klei Sousa for the line drawing, to Ana Carolina D. Castello
for the distribution map, and to the reviewers for the valuable contributions.
VISMIA CONDUPLICATA (HYPERICACEAE) Phytotaxa 338 (1) © 2018 Magnolia Press 129
References
Bachman, S., Moat, J., Hill, A.W., Torre, J. & Scott, B. (2011) Supporting Red List threat assessments with GeoCAT: geospatial conservation
assessment tool. ZooKeys 150: 117–126.
http://dx.doi.org/10.3897/zookeys.150.2109
Berg, M.E. van den (1970) Uma espécie e duas variedades novas de Guttiferae da Amazônia. Boletim do Museu Paraense Emílio Goeldi.
Nova série, Botânica 38: 1–6.
Ewan, J. (1962) Synopsis of the South American species of Vismia (Guttiferae). Contributions from the United States National Herbarium
35: 293–377.
http://dx.doi.org/10.5962/bhl.part.6208
Flora do Brasil 2020 em construção (2017) Hypericaceae. Jardim Botânico do Rio de Janeiro. Available from: http://floradobrasil.jbrj.gov.
br/reflora/floradobrasil/FB133/ (accessed 20 June 2017)
Gustafsson, M.H.G. (2017) Neotropical Hypericaceae. In: Neotropikey - Interactive key and information resources for flowering plants
of the Neotropics. Available from: http://www.kew.org/science/tropamerica/neotropikey/families/Hypericaceae.htm (accessed 14
August 2017)
Marimon, B.S., Marimon-Junior, B.H., Mews, H.A., Jancoski, H.S., Franczak, D.D., Lima, H.S., Lenza, E., Rossete, A.N. & Moresco,
M.C. (2012) Florística dos campos de murundus do Pantanal do Araguaia, Mato Grosso, Brasil. Acta Botanica Brasilica 26: 181–
196.
http://dx.doi.org/10.1590/S0102-33062012000100018
Marimon, B.S., Colli, G.R., Marimon-Junior, B.H., Mews, H.A., Eisenlohr, P.V., Feldpausch, T.R. & Phillips, O.L. (2015) Ecology of
floodplain campos de murundus savanna in Southern Amazonia. International Journal of Plant Sciences 176: 670–681.
http://dx.doi.org/10.1086/682079
Oliveira-Filho, A.T. (1992) The vegetation of Brazilian ‘murundus’ – the island-effect on the plant community. Journal of Tropical Ecology
8: 465–486.
http://dx.doi.org/10.1017/S0266467400006817
Reichardt, H.W. (1878) Hypericaceae. In: Martius, C.F.P., Eichler, A.W. & Urban, I. (Eds.) Flora brasiliensis. Vol. 12, part 1. Frid.
Fleischer, Leipzig, pp. 182–212.
http://dx.doi.org/10.5962/bhl.title.454
Ribeiro, J.F. & Walter, B.M.T. (2008) As principais fitofisionomias do bioma Cerrado. In: Sano, S.M., Almeida, S.P. & Ribeiro, J.F. (Eds.)
Cerrado: ecologia e flora. Embrapa Cerrados/Embrapa Informação Tecnológica, Brasília, pp. 151–199.
Robson, N.K.B. (1998) Vismia. In: Steyermark, J.A., Berry, P.E. & Holst, B.K. (Eds.) Flora of the Venezuelan Guayana. Vol. 4. Missouri
Botanical Garden Press, Saint Louis, pp. 322–329.
Saint-Hilaire, A. (1828) Flora Brasiliae meridionalis. Vol. 1, part 9. A. Belin, Paris, pp. 321–360.
Silva, L.C.R., Vale, G.D., Haidar, R.F. & Sternberg, L.S.L. (2010) Deciphering earth mound origins in central Brazil. Plant and Soil 336:
3–14.
https://doi.org/10.1007/s11104-010-0329-y
Stevens, P.F. (2007) Hypericaceae. In: Kubitzki, K. (Ed.) The families and genera of vascular plants. Vol. 9. Springer, Berlin, 194–201.
http://dx.doi.org/10.1007/978-3-540-32219-1_24
Thiers, B. (2017) [continuously updated] Index Herbariorum: A global directory of public herbaria and associated staff. New York
Botanical Garden’s Virtual Herbarium. Available from: http://sweetgum.nybg.org/science/ih/ (accessed 20 June 2017)
Vandelli, D. (1788) Florae Lusitanicae et Brasiliensis specimen et epistolae ab eruditis viris Carolo a Linné, Antonio de Haen ad
Dominicum Vandelli scriptae. Typographia Academico-Regia, Coimbra, 96 pp.
http://dx.doi.org/10.5962/bhl.title.51092
... Some of them are popularly known in Brazil as "lacre" and "pau-de-lacre" (meaning "seal" or "sealing wax" and "sealing stick", respectively). These common names are due to their distinctive exudates, which are often reddish-orange, yellowish-orange, or orange (Martins et al., 2018b;Vogel Ely et al., 2023). Anthraquinones, anthrones, xanthones and benzophenones, frequently isolated from these plants, are lipophilic compounds that contribute to the color of the exudates (Diel et al., 2021). ...
... Due to the increase in deforestation in the Mato Grosso state on the last years in areas of Legal Amazon (INPE 2020), the knowledge gaps in Amazon biome, the lack of funding for collecting projects and longterm storage of the resulting reference collections (Zappi et al. 2016), it is likely that its biodiversity is underestimate. This has been demonstrated by the amount of recent studies describing new taxa (e.g., Petini-Benelli and Soares-Lopes 2015; Engels et al. 2016;Pellegrini et al. 2016;Pessoa et al. 2016;Daly 2017;Engels and Canestraro 2017;Labiak et al. 2018;Martins et al. 2018;Engels et al. 2019;Koch et al. 2019;Sagella and Calonje 2019;Bohn et al. 2020;Silva et al. 2020) and showing new distribution records (e.g., Zappi et al. 2011;Moura 2016;Zappi et al. 2016;Ferneda Rocha and Engels 2017;Engels and Marinho 2018;. Thereby, the description of this new species contributes and expands the floristic knowledge from northern Mato Grosso State, in the south edge of Brazilian Amazon, an area that still below its real richness and diversity. ...
Article
Mormodes matogrossensis, a new epiphytic orchid species is described and illustrated from the Floresta Estacional Sempre Verde along the Teles Pires River in southern Brazilian Amazon. This species belongs to M. sect. Mormodes and is similar to M. vinacea and M. paraënsis but differs by the lip lanceolate-trullate with basal lateral lobes, which are rounded and inconspicuously obtuse. We provided description, taxonomic and ecological comments, state of conservation, geographic distribution map, illustrations of the new species.
... No Brasil ocorrem dois gêneros: Hypericum L., com 23 espécies e maior diversidade no sul do país, e Vismia Vand., com 30 espécies e maior diversidade na região amazônica (Martins et al. 2018, Flora do Brasil 2020. O gênero Vismia foi estabelecido por Domingos Vandelli (1788), que o segregou de Hypericum por apresentar características como pétalas e nectários pilosos. ...
Article
Full-text available
RESUMO São apresentadas as espécies de Hypericaceae registradas para a Reserva Ducke, Estado do Amazonas, incluindo chave de identificação, descrições, ilustrações, comentários sobre distribuição geográfica e hábitats. A família está representada na área por cinco espécies do gênero Vismia: Vismia cauliflora, V. cayennensis, V. guianensis, V. japurensis e V. sandwithii.
Article
Vismia is a neotropical genus and in Brazil it is currently represented by 30 species. Along with the study of the species that occur in this country, we assessed the nomenclatural questions involved with their names, and a first part of these results are presented. Twelve lectotypes, including one as a second-step, were designated for correct names and synonyms associated with eleven species of Vismia. Furthermore, we provided additions and corrections to the collection data, and nomenclatural comments for each species. Here we also reduce V. parviflora to a synonym of V. micrantha, based on morphological characters.
Article
Full-text available
The present study provides an overview, focusing on the botanical aspects, phytochemistry, ethnopharmacology and biological activities reported for species from the tribe Vismieae (Hypericaceae). These species, traditionally distributed in three genera (Vismia, Psorospermum and Harungana), occur predominantly in tropical areas of South America, mainland Africa and Madagascar, where several of them are used in the traditional medicine mainly as febrifugal, antimalarial and for treating wounds of diverse origin. The phytochemical investigations indicated that the plants produce anthraquinones, anthrones, xanthones, benzophenones, flavonoids and some terpenoids. A number of 221 different compounds were obtained from 32 species of the tribe. Several compounds were investigated for the pharmacological activities, being cytotoxic and antimicrobial the most cited. Nevertheless, a number of pharmacological researches were carried out with extracts and some findings experimentally evidenced the ethnopharmacological usefulness of several species. The distribution of the anthracenic derivatives, xanthones and benzophenone precursors is not uniform in the genera. Thus, the substitution pattern of these compounds was analyzed and the systematic relationship among the taxa is discussed in the light of these features. Of note, more species need chemical investigation in order to make a judgment about the taxonomic significance of the compounds, but it seems that, although the tribe has a certain homogeneity, each genus has particularities. Considering this statement, it is possible to say that in the chemical point of view, Psorospermum is diferent from Harungana and both are diferent from Vismia, which is clearly separate into two distinct groups, the African and the American species.
Chapter
Full-text available
Este capítulo analisa e descreve as principais fitofisionomias ocorrentes no bioma (ou domínio) do Cerrado. São descritos 11 tipos de vegetação principais, enquadrados em formações florestais (4 tipos), savânicas (4 tipos) e campestres (3 tipos). Considerando também os subtipos, neste sistema são reconhecidas 25 fitofisionomias.
Article
Full-text available
O presente estudo teve como objetivo determinar e comparar a riqueza e a composição de espécies de angiospermas entre campos de murundus (CM) do Parque Estadual do Araguaia (PEA), em uma das maiores planícies de inundação do Brasil. O PEA localiza-se em Novo Santo Antônio, Mato Grosso, sendo delimitado a leste pelo Rio Araguaia e a oeste pelo Rio das Mortes. Foram realizadas coletas intensivas da flora em 11 hectares, e áreas adjacentes, de CM distribuídos ao longo do PEA. Estudos do meio físico foram realizados através de descrições in situ. Os solos são do tipo Plintossolo, hidromórficos minerais, profundos, imperfeitamente a mal drenados, com baixa permeabilidade. No total foram coletadas 318 espécies, 193 gêneros e 66 famílias. Nos CM os valores variaram de 51 a 135 espécies, 42 a 107 gêneros e 27 a 52 famílias. Erythroxylum suberosum foi considerada uma espécie típica de CM brasileiros, Curatella americana típica de CM de Mato Grosso e Byrsonima cydoniifolia típica do PEA. O padrão físico e de distribuição espacial dos murundus pode ser um reflexo do pulso de inundação sazonal, visto que a composição florística dos campos de murundus variou entre as áreas de influência dos rios que delimitam o parque. Este foi o maior levantamento florístico já realizado em CM, permitindo relevante ampliação do conhecimento e registro de espécies típicas do Bioma Cerrado e que ocorrem nessa fitofisionomia.
Article
Full-text available
The ‘campos de murundus’ (carthmound fields) are typical landscapes of the cerrado (savanna) region of Central Brazil and are characterized by many rounded earthmounds called ‘murundus’ which are scattered over a grassland surface. As these areas are normally liable to seasonal water-logging, the earthmounds are true habitat islands capable of bearing woody plants typical of the cerrado, which are normally very intolerant of root inundation. The vegetation of an area of murundus field at Cuiaba, in the State of Mato Grosso, Central Brazil, was surveyed for the purpose of evaluating the island-effect on the plant community growing on the mounds/islands. Two main aspects were considered: the influence of the size of the mound and the differences between the types of cerrado occurring on the mounds and on the areas surrounding the murundus field. Most plant species occurring on the mounds were also present in the flora of the surrounding cerrado. However, only a fraction of these species was able to colonize the mounds successfully. The number of species on the mounds was found to be significantly correlated with mound area. Speciesarea relationships were better described with the power model S = C(Az) than with the exponential model S = C + z (logA) (fitted with linear regression). The mound size also had a strong influence on the spatial distribution of the species on the surface of the mounds. The species were organized in an increasing number of concentric topographic belts corresponding to a gradient of soil depth above the Hooding level.
Article
Full-text available
Mound fields are a common landscape throughout the world and much of the evidence for their origin has been of a circumstantial nature. It has been hypothesized that earth mounds emerge over grasslands by termite activity; alternatively, they might be formed after erosion. We tested whether a mound field in central Brazil was generated by termite activity or erosion. We used soil organic matter isotopic composition, soil chemical, physical and floristic composition to determine the origin of a mound field. If the mounds emerged by termite activity in an established grassland the soil organic matter below the mound should have the isotopic signature of C4 dominated grassland, which contrasts with savanna C3 + C4 signature. Additionally, soil traits should resemble those of the grassland. All markers indicate that the mounds were formed by erosion. The soil isotopic composition, chemical traits and texture below the mound resembled those of the savanna and not those of the grassland. Moreover, most of the species present in the mound were typical of savanna. Concrete evidence is provided that mound fields in the studied area were produced by erosion of a savanna ecosystem and not termite activity. The use of the techniques applied here would improve the assessments of whether analogous landscapes are of a biogenic nature or not. KeywordsCarbon isotope-Soil-Erosion-Savanna-Termites- murundus
Article
Full-text available
GeoCAT is an open source, browser based tool that performs rapid geospatial analysis to ease the process of Red Listing taxa. Developed to utilise spatially referenced primary occurrence data, the analysis focuses on two aspects of the geographic range of a taxon: the extent of occurrence (EOO) and the area of occupancy (AOO). These metrics form part of the IUCN Red List categories and criteria and have often proved challenging to obtain in an accurate, consistent and repeatable way. Within a familiar Google Maps environment, GeoCAT users can quickly and easily combine data from multiple sources such as GBIF, Flickr and Scratchpads as well as user generated occurrence data. Analysis is done with the click of a button and is visualised instantly, providing an indication of the Red List threat rating, subject to meeting the full requirements of the criteria. Outputs including the results, data and parameters used for analysis are stored in a GeoCAT file that can be easily reloaded or shared with collaborators. GeoCAT is a first step toward automating the data handling process of Red List assessing and provides a valuable hub from which further developments and enhancements can be spawned.
Article
Premise of research. This represents one of the first studies of the ecology, diversity, and structure of campos de murundus termite savannas in the vast seasonal wetlands of southern Amazonia. We aimed to improve understanding of this threatened system by assessing species richness, abundance, and co-occurrence among trees and herbs of murundus (earth mounds), investigating the environmental and biological mechanisms underlying these patterns, and discussing implications for biodiversity conservation. Methodology. We identified every tree, shrub, subshrub, and herb on 373 murundus across 11 ha at Araguaia State Park, southern Amazonia. We constructed species abundance distributions of trees and herbs, assessed best-fit models, and tested for nonrandom patterns of species co-occurrence using checkerboard scores. Using detrended correspondence analysis (DCA), we assessed the affinities among tree species and their positions in murundus. Pivotal results. A total of 166 species, 123 genera, and 49 families occupied the murundus. The species abundance distribution of trees followed a lognormal distribution, whereas that of herbs was best described by a Mandelbrot distribution. Observed C-score indices for trees and herbs were significantly larger than expected by chance, indicating nonrandom distributions and species segregation among murundus. DCA revealed a strong gradient in species occurrence within murundus, suggesting that internal structuring may be hydrologically based (e.g., variation in mound microrelief). Conclusions. Environmental (e.g., flooding) and biological (e.g., competition between plants) factors are important for controlling the occurrence of tree and herb species on the murundus. The murundus function as critical bases for the maintenance of species diversity in this extensive floodplain, thereby deserving recognition among ecosystems with high conservation priorities.
Chapter
Evergreen or sometimes deciduous herbs, shrubs or trees; glands or canals in most parts of the plant; xanthones widespread; hairs uni- or multicellular, eglandular, colleters common; terminal bud scaly or naked; leaves opposite, occasionally whorled or alternate, entire, estipulate; in florescences terminal, more or less cymose, rarely axillary or flowers single, flowers polysymmetric, perfect, usually with prophylls; sepals free, (2-)4-5; petals (3)4-5, free; stamens (9-)∞, freeorvariously fasciculate or connate, anthers < 1(-1.2)mm long, dithecate, extrose, opening by slits, connective often with glands, staminodes alternipetalous or 0; nectary absent; ovary superior, 3-5-locular, placentation axile to parietal, ovules 1-∞/carpel, anatropous, bitegmic, tenuinucellate; stylodia free or basally more or less fused or style single, stigmas more or less expanded, smooth and sticky or ±punctate and papillate; fruit baccate or capsular, rarely a drupe; seeds small, winged or not, exotegmen lignified, with sinuous anticlinal walls; embryo straight or rarely curved; endosperm initially nuclear, often absent at maturity; germination epigeal, phanerocotylar.
Uma espécie e duas variedades novas de Guttiferae da Amazônia. Boletim do Museu Paraense Emílio Goeldi. Nova série
  • M E Berg
  • Van Den
Berg, M.E. van den (1970) Uma espécie e duas variedades novas de Guttiferae da Amazônia. Boletim do Museu Paraense Emílio Goeldi. Nova série, Botânica 38: 1-6.
Synopsis of the South American species of Vismia (Guttiferae)
  • J Ewan
Ewan, J. (1962) Synopsis of the South American species of Vismia (Guttiferae). Contributions from the United States National Herbarium 35: 293-377.
) Hypericaceae. Jardim Botânico do Rio de Janeiro Available from: http://floradobrasil.jbrj.gov. br/reflora
  • Flora
Flora do Brasil 2020 em construção (2017) Hypericaceae. Jardim Botânico do Rio de Janeiro. Available from: http://floradobrasil.jbrj.gov. br/reflora/floradobrasil/FB133/ (accessed 20 June 2017)