With contributions by: Abreu, Maria C.; Acevedo-Rodríguez, Pedro; Agra, Maria F.; Almeida Jr., Eduardo B.; Almeida, Gracineide S.S.; Almeida, Rafael F.; Alves, Flávio M.; Alves, Marccus; Alves-Araujo, Anderson; Amaral, Maria C.E.; Amorim, André M.; Amorim, Bruno; Andrade, Ivanilza M.; Andreata, Regina H.P.; Andrino, Caroline O.; Anunciação, Elisete A.; Aona, Lidyanne Y.S.; Aranguren, Yani; Aranha Filho, João L.M.; Araújo, Andrea O.; Araújo, Ariclenes A.M.; Araújo, Diogo; Arbo, María M.; Assis, Leandro; Assis, Marta C.; Assunção, Vivian A.; Athiê-Souza, Sarah M.; Azevedo, Cecilia O.; Baitello, João B.; Barberena, Felipe F.V.A.; Barbosa, Maria R.V.; Barros, Fábio; Barros, Lucas A.V.; Barros, Michel J.F.; Baumgratz, José F.A.; Bernacci, Luis C.; Berry, Paul E.; Bigio, Narcísio C.; Biral, Leonardo; Bittrich, Volker; Borges, Rafael A.X.; Bortoluzzi, Roseli L.C.; Bove, Cláudia P.; Bovini, Massimo G.; Braga, João M.A.; Braz, Denise M.; Bringel Jr., João B.A.; Bruniera, Carla P.; Buturi, Camila V.; Cabral, Elza; Cabral, Fernanda N.; Caddah, Mayara K.; Caires, Claudenir S.; Calazans, Luana S.B.; Calió, Maria F.; Camargo, Rodrigo A.; Campbell, Lisa; Canto-Dorow, Thais S.; Carauta, Jorge P.P. †; Cardiel, José M.; Cardoso, Domingos B.O.S.; Cardoso, Leandro J.T.; Carneiro, Camila R.; Carneiro, Cláudia E.; Carneiro-Torres, Daniela S.; Carrijo, Tatiana T.; Caruzo, Maria B.R.; Carvalho, Maria L.S.; Carvalho-Silva, Micheline; Castello, Ana C.D.; Cavalheiro, Larissa; Cervi, Armando C. †; Chacon, Roberta G.; Chautems, Alain; Chiavegatto, Berenice; Chukr, Nádia S.; Coelho, Alexa A.O.P.; Coelho, Marcus A.N.; Coelho, Rubens L.G.; Cordeiro, Inês; Cordula, Elizabeth; Cornejo, Xavier; Côrtes, Ana L.A.; Costa, Andrea F.; Costa, Fabiane N.; Costa, Jorge A.S.; Costa, Leila C.; Costa-e-Silva, Maria B.; Costa-Lima, James L.; Cota, Maria R.C.; Couto, Ricardo S.; Daly, Douglas C.; De Stefano, Rodrigo D.; De Toni, Karen; Dematteis, Massimiliano; Dettke, Greta A.; Di Maio, Fernando R.; Dórea, Marcos C.; Duarte, Marília C.; Dutilh, Julie H.A.; Dutra, Valquíria F.; Echternacht, Lívia; Eggers, Lilian; Esteves, Gerleni; Ezcurra, Cecilia; Falcão Junior, Marcus J.A.; Feres, Fabíola; Fernandes, José M.; Ferreira, D.M.C.; Ferreira, Fabrício M.; Ferreira, Gabriel E.; Ferreira, Priscila P.A.; Ferreira, Silvana C.; Ferrucci, Maria S.; Fiaschi, Pedro; Filgueiras, Tarciso S.; Firens, Marcela; Flores, Andreia S.; Forero, Enrique; Forster, Wellington; Fortuna-Perez, Ana P.; Fortunato, Reneé H.; Fraga, Cláudio N.; França, Flávio; Francener, Augusto; Freitas, Joelcio; Freitas, Maria F.; Fritsch, Peter W.; Furtado, Samyra G.; Gaglioti, André L.; Garcia, Flávia C.P.; Germano Filho, Pedro; Giacomin, Leandro; Gil, André S.B.; Giulietti, Ana M.; Godoy, Silvana A.P. ; Goldenberg, Renato; Gomes da Costa, Géssica A.; Gomes, Mário; Gomes-Klein, Vera L.; Gonçalves, Eduardo Gomes; Graham, Shirley; Groppo, Milton; Guedes. Juliana S.; Guimarães, Leonardo R.S.; Guimarães, Paulo J.F.; Guimarães, Elsie F.; Gutierrez, Raul; Harley, Raymond; Hassemer, Gus...

Resumo No final da década de 1960, pesquisadores do Museu Paraense Emílio Goeldi (MPEG) iniciaram as coletas botânicas na Serra dos Carajás, resultando em um expressivo acervo e interessantes descobertas sobre a flora local, marcada por endemismos e pressão por atividades mineradoras. Em 2014, foi estabelecido o projeto "Flora das cangas da Serra dos Carajás" através da cooperação entre o MPEG e o Instituto Tecnológico Vale de Desenvolvimento Sustentável (ITVDS), visando especialmente a elaboração da flora das cangas da FLONA Carajás. Um acervo de cerca de quinze mil exsicatas, depositadas principalmente nos herbários MG e BHCB além de HCJS, INPA, IAN, NY e RB constitui a base para o desenvolvimento da flora. Até o momento, a flora inclui 151 famílias de angiospermas, gimnospermas, licófitas e samambaias e briófitas (musgos e hepáticas). Neste trabalho apresentamos um breve histórico dos estudos botânicos na região, caracterização da área de estudo, e procedimentos metodológicos adotados no desenvolvimento do projeto. Também, constitui a introdução para o volume 1 da Flora das cangas de Carajás composto por 55 famílias, sendo quatro de briófitas, duas de licófitas, oito de samambaias, uma de gimnospermas e 40 de angiospermas, incluindo 139 gêneros e 248 espécies.

Resumo Nas cangas da Floresta Nacional (FLONA) de Carajás e no Parque Nacional dos Campos Ferruginosos (PNCF) foram registradas 856 espécies, distribuídas em 116 famílias de fanerógamas. As famílias mais ricas foram Poaceae (86), Fabaceae (65) e Rubiaceae (46). O hábito herbáceo foi o melhor representado. Dois gêneros, 24 espécies e uma subespécie são apontadas como endêmicas das cangas da área de estudos. Na FLONA de Carajás, a Serra Norte, com maior amostragem, possui 659 espécies de fanerógamas e na Serra Sul foram registradas 545 espécies. Aproximadamente 60% das espécies documentadas na área de estudos, incluindo espécies endêmicas, não possuem registro para o PNCF. Através da lista taxonômica aqui apresentada, foi possível demonstrar considerável distinção entre as cangas da Serra dos Carajás e as do Quadrilátero Ferrífero, em Minas Gerais, apontando também pouca correspondência dessas duas listas com a canga de Corumbá, no Mato Grosso do Sul. A riqueza e singularidade da flora da região, que inclui diversas espécies endêmicas, associada à ameaça a que estão submetidos estes ambientes por atividades de mineração, apontam para a necessidade de um planejamento para conservação das espécies da flora das cangas de Carajás.

Amazonia is one of the most diverse biomes worldwide, and, as well as luxuriant forest, it includes mountain areas which, despite their small surface area, display fascinating endemism. In these regions, the specificity of edaphic factors is mirrored by a highly specialised, isolated flora adapted to survive adverse conditions. The Serra dos Carajás in the Brazilian state of Pará is one of world's largest iron ore reserves. Known locally as canga, this ironstone formation occupies an area of 115.9 km 2 , and supports campo rupestre of canga vegetation on outcrops that are mostly in the Floresta Nacional de Carajás (FLONA of Carajás) and Parque Nacional dos Campos Ferruginosos (PNCF). The recent publication of the Flora of the cangas of Carajás lists 856 species of seed plants and 186 species of ferns and lycophytes. This project assessed the canga endemic species growing in the region, and further expeditions guided by SDM were carried out in order to ascertain their distribution outisde the area. Departing from an initial list of 58 putative endemics, the final list comprises 38 species of vascular plants (c. 4% of the local flora). These are distributed in 31 genera and 22 families, including three monotypic genera: Carajasia (Rubiaceae), Monogereion and Parapiqueria (Asteraceae). From these, 24 are classified as Rare Species for Brazil and seven as Highly Restricted Endemic (EEO < 100 km 2). An illustrated account is provided, as well as further SDM to detect other possible areas of distribution based on the studied species. The knowledge generated is aimed at directing appropriate conservation plans for the area.

No abstract

In order to establish effective conservation strategy, drivers of local and regional patterns of biodiversity need to be understood. The composition of local biodiversity is dependent on a number of factors including evolution and redistribution of lineages through dispersal and environmental heterogeneity. Brazilian canga is characterised by a ferrugineous substrate, found both in the Iron Quadrangle of Minas Gerais and in the Carajás mountains in Amazonia. Canga is one of several specialised habitat types comprising Brazilian campo rupestre , a montane vegetation found within or adjacent to several major Brazilian bioregions, including the Atlantic Forest and Amazonia, with exceptionally high levels of diversity and endemism arising from both history of dispersal and environmental variation. In order to inform biodiversity conservation for canga , and more broadly for campo rupestre , we performed floristic and phylogenetic analyses investigating affinities between 28 sites on different substrates ( canga and quartzite) and geographic locations (Carajás, Pará [Amazonia]; Cadeia do Espinhaço, Minas Gerais; Chapada Diamantina, Bahia). Through analysis of 11204 occurrences of 4705 species of angiosperms, we found that Amazonian Carajás canga plant communities formed a cohesive group, distinct from species assemblages found in Eastern Brazil (Minas Gerais, Bahia), either on canga or quartzite. The phylogenetic megatree of species across all sites investigated shows associations between certain clades and Amazonian canga , with few shared species between the Amazonian Carajás and Eastern Brazil sites, while the floristic comparison shows high levels of heterogeneity between sites. The need for reserves for Amazonian Carajás canga has been recognized and addressed by the creation of a national park. However, current sampling does not provide sufficient reassurance that the canga areas now benefitting from full legal protection adequately represent the regional canga flora.

Open habitats such as grasslands occupy &lt; 5% of the Amazon and are currently grouped under the broad term Amazonian savanna, covering an area of c. 267 000 km2, mostly in Brazil and Bolivia. These habitats are found isolated within an extensive rainforest matrix, having a distinct flora from the latter. The lower Amazon River is home to several patches of savanna that occupy both south and north banks of the river, in Santarém, Alenquer and Monte Alegre. Although having an abundance of herbaceous plants, most studies on these open areas focus only on tree species, ignoring the relevant non-woody component of the vegetation. Our objectives were to provide new surveys of seed plants for two Amazonian savanna sites and to take the opportunity to revisit the biogeographical links between Amazonian savanna, Amazonian canga vegetation and the central Brazilian cerrado (CBC) and caatinga, analysing woody and herbaceous plants. We created a floristic database that includes sites of Amazonian savannas, including campinarana, coastal scrub (restinga), CBC and Amazonian campos rupestres (on canga or other substrate). We compared those sites using multivariate analyses to find out the degree of floristic resemblance between sites. We prepared a new list of 406 species of seed plants [336 in Parque Estadual de Monte Alegre (PEMA) and 117 in Serra do Itauajuri (SI)], including 23 new records for the state of Pará and some putative new species for science. The Amazonian savannas form three loosely arranged groups, whereas the Amazonian canga formed a cohesive assemblage. Both groups were contrasted against cerrado and caatinga sites and had a distinctive flora from both. Sites from north-western Pará (Alter do Chão, PEMA and SI) were grouped with their northern counterparts in Roraima. An improved representation of the flora of these sites is provided, with more insight into the relationship between the Amazonian savanna sites and other vegetation types. It is worrying that recent changes of the Brazilian legislation place open environments, such as PEMA, in the path of vulnerability to disturbance and destruction.

Isoetes are ancient quillworts members of the only genus of the order Isoetales. The genus is slow evolving but is resilient, and widespread worldwide. Two recently described species occur in the Eastern Brazilian Amazon, Isoetes serracarajensis and Isoetes cangae. They are found in the ironstone grasslands known as Canga. While I. serracarajensis is present mostly in seasonal water bodies, I. cangae is known to occur in a single permanent lake at the South mountain range. In this work, we undertake an extensive morphological, physiological and genetic characterization of both species to establish species boundaries and better understand the morphological and genetic features of these two species. Our results indicate that the morphological differentiation of the species is subtle and requires a quantitative assessment of morphological elements of the megaspore for diagnosis. We did not detect differences in microspore output, but morphological peculiarities may establish a reproductive barrier. Additionally, genetic analysis using DNA barcodes and whole chloroplast genomes indicate that although the plants are genetically very similar both approaches provide diagnostic characters. There was no indication of population structuring I. serracarajensis. These results set the basis for a deeper understanding of the evolution of the Isoetes genus.