PHYTOTAXA ISSN (online edition)

Similar documents
Common Name: GEORGIA QUILLWORT. Scientific Name: Isoetes georgiana Luebke. Other Commonly Used Names: none. Previously Used Scientific Names: none

Other Commonly Used Names: wintergreen quillwort, evergreen quillwort

PTERIS REPTANS (PTERIDACEAE) - A NEW RECORD FOR INDIA

A New Locality of Fossombronia mylioides (Fossombroniaceae, Marchantiophyta)

Isoetes yunguiensis (Isoetaceae), a New Basic Diploid Quillwort from China

Common Name: BLACK-SPORED QUILLWORT. Scientific Name: Isoetes melanospora Engelmann. Other Commonly Used Names: black-spored Merlin's grass

SOLIDAGO SPELLENBERGII (ASTERACEAE: ASTEREAE), A NEW SPECIES OF GOLDENROD FROM MEXICO

Weather Report 31 January 2018

ISOETES TEXANA (ISOETACEAE): A NEW SPECIES FROM THE TEXAS COASTAL BEND

Alcantarea galactea (Bromeliaceae), a New Giant Bromeliad from Brazil, with Populations Seen from the Sky

Asparagus bojnurdensis (Asparagaceae), a new species from Iran

Digital Key to the Flora of Mongolia

Regional Flora- Introduction to Plant Taxonomy. Plant taxonomy. Taxonomists use information about: -structure. -chemical composition.

SEED COAT AND FRUIT SURFACE MICROMORPHOLOGY OF SOME CYNOGLOSSUM L. (BORAGINACEAE) SPECIES OZNUR ERGEN AKCIN

ON SOLIDAGO MACVAUGHII (ASTERACEAE: ASTEREAE), A RARE MEXICAN ENDEMIC OF THE TORTIFOLIAE GROUP OF SOLIDAGO. SUBSECT. TRIPLINERVIAE

CURRENT CONCEPTS IN PLANT TAXONOMY

Biologists use a system of classification to organize information about the diversity of living things.

Topic 22. Introduction to Vascular Plants: The Lycophytes

The taxonomic status of Fontinalis mollis and F. antipyretica var. cymbifolia with the description of Fontinalis antipyretica var.

ANTHER TYPES OF THE MONOCOTS WITHIN FLORA OF KARACHI, PAKISTAN

Plant Crib VERONICA. 1. Veronica serpyllifolia

CLASS XI BIOLOGY NOTES CHAPTER 1: LIVING WORLD

Second Year Annual Report - Botany

Gülay Ecevit Genç & Emine Akalın. Comparison between two Eryngium from Turkey: E. heldreichii and E. davisii. Introduction

PHYTOTAXA ISSN (online edition)

Introduction by Francis Underwood

SYLLABUS THEME B PLANT CLASSIFICATION & DIVERSITY INTRODUCTION TO TAXONOMY HISTORICAL DEVELOPMENT

Mapping Brazil in 1:250,000 scale. João Bosco de Azevedo

Creating an e-flora for South Africa

SEM studies on fruit and seed of some Chenopodium L. species (Chenopodiaceae)

ROSTANIHA. Kickxia iranica, a new species from Iran Received: / Accepted: Kickxia iranica

Plant Names and Classification

Part 1: Naming the cultivar

An Unexpected Mcvaughia (Malpighiaceae) Species from Sandy Coastal Plains in Northeastern Brazil

Common Name: FLORIDA ADDER S-MOUTH ORCHID. Scientific Name: Malaxis spicata Swartz. Other Commonly Used Names: none

Isoetes pedersenii, a new species from Southern South America

Mosquito Systematics Vol. 6(Z) June 1974

CHAPTER-1 THE LIVING WORLD MULTIPLE CHOICE QUESTIONS

Microthyriales of Tierra del Fuego I: The Genus Parasterinella SPEGAZZINI

YUCCA FREEMANII (ASPARAGACEAE) NEW TO ARKANSAS

Georgia Performance Standards for Urban Watch Restoration Field Trips

APPLICATIONS UNDER EXAMINATION. MAGNOLIA (Magnolia) Proposed denomination: Cleopatra Application number: Application date: 2011/02/25

CONTRIBUTIONS TOWARD A REVISION OF HECHTIA (BROMELIACEAE, PITCAIRNIOIDEAE) II. NEW AND NOTEWORTHY HECHTIA SPECIES FROM OAXACA, MÉXICO

A new species of Bertiella (Melanommataceae) from Brazil and a key to accepted species

The name of a species consisted of a generic name (noun) followed by 1 or more Latin modifiers.

Print Names and Classification

SPECIES FACT SHEET Common Name: Scientific Name: Technical Description: Distinctive characters: Similar species:

ecotones during the late Holocene in lowland South America

Two new species in Hippotis (Rubiaceae) from Ecuador and Peru. Melissa Calderón University of Puerto Rico- Río Piedras Mentor: Charlotte M.

Two new species of Cryptophagus HERBST, 1792 (Coleoptera: Cryptophagidae) from New Mexico (United States of America)

Three Monte Carlo Models. of Faunal Evolution PUBLISHED BY NATURAL HISTORY THE AMERICAN MUSEUM SYDNEY ANDERSON AND CHARLES S.

SPECIES FACT SHEET. Taxonomic Note: None.

Motivation for project:

HIOLOGX

06/09/05. A survey of the plant kingdom based on a detailed study of the morphology, anatomy and physiology of selected representative specimens.

Seed morphology diversity in some Iranian endemic Silene (Caryophyllaceae) species and their taxonomic significance

DRABA RAMOSISSIMA (BRASSICACEAE) NEW TO ALABAMA

EXPONENTIAL INCREASE IN DESCRIPTION RESOLUTION

Billie L. Turner Plant Resources Center The University of Texas, Austin, TX ABSTRACT

Managing Mycological Mysteries

CropCast Corn and Soybean Report Kenny Miller Monday, March 13, 2017

EFFICIENCY SIMULATION OF A HPGE DETECTOR FOR THE ENVIRONMENTAL RADIOACTIVITY LABORATORY/CDTN USING A MCNP-GAMMAVISION METHOD

COMMENTS ON THE CONSERVATION STATUS OF SENECIO VELLEIOIDES (FOREST GROUNDSEL) IN TASMANIA

Weather Report 29 November 2017

The seed coat and pollen morphology of Gypsophila pilosa (Caryophyllaceae)

Weather Report 04 April 2018

GUAMA RIVER AND GUAJARA BAY, BELEM - AMAZON REGION

The Petiolar Structure of Christella dentata (Forssk.) Brownsey & Jermy (Thelypteridaceae, Pteridophyta)

Type studies on Pycnolejeunea (Lejeuneaceae, Hepaticae), III. Two Asiatic species described by Hoffmann

The Living World. AIIMS,CBSE,AIPMT, AFMC,Bio.Tech & PMT, Contact : , Mail at :- by AKB

Common Name: SHOALS SPIDER-LILY. Scientific Name: Hymenocallis coronaria (J. LeConte) Kunth. Other Commonly Used Names: Cahaba lily, Catawba lily

George Yatskievych Missouri Botanical Garden P.O. Box 299 Saint Louis, MO

Ontario Science Curriculum Grade 9 Academic

FLORA OF NEW ZEALAND FERNS AND LYCOPHYTES

PHYTOTAXA ISSN (online edition)

Revisions Of The Palm Genus Syagrus Mart. And Other Selected Genera In The Cocos Alliance (Illinois Biological Monographs, No. 56) By Sidney F.

Identification of Balsam poplars - 1

Phaeocalicium populneum

Morphological comparison and key to Juniperus deltoides and J. oxycedrus

TWO NEW BERBERIS SECTION WALLICHIANAE FROM WESTERN CHINA 730. BERBERIS YINGJINGENSIS Berberidaceae. Julian Harber

Amphigomphus somnuki n. sp. from North Thailand (Odonata: Gomphidae) MATTI HAMALAINEN

THE OHIO JOURNAL OF SCIENCE

Polygonum caespitosum (Bristled knotweed Bunchy knotweed Oriental ladysthumb )

Taxonomy and Systematics: a broader classification system that also shows evolutionary relationships

Equisetaceae Horsetails

Unit 5.2. Ecogeographic Surveys - 1 -

A handful of primary features are useful for distinguishing water primrose (Ludwigia) from other plants. Understand what to look for, such as leaf

POLLEN ANALYSIS - terminology

Selaginella P. Beauv. from Minas Gerais, Brazil

Weather Report 30 November 2017

Previously Used Scientific Names: Viburnum dentatum L. var. bracteatum

Svetlana Bancheva & Zafer Kaya. Centaurea raimondoi, a new species from Asteraceae. Introduction

Common Name: GLADE WINDFLOWER. Scientific Name: Anemone berlandieri Pritzel. Other Commonly Used Names: southern thimble-weed

A new combination and a new species in Phlegmariurus (Herter) Holub (Lycopodiaceae) from Southern Vietnam

THERMAL HYDRAULIC MODELING OF THE LS-VHTR

The genus Anthurium in Central America morphology, ecology, and evolution

TECHNICAL DOCUMENT R 2 OF THE SPANISH BRAILLE COMMISSION GENERAL CRITERIA FOR PREPARING ADAPTED MAPS FOR VISUALLY IMPAIRED PERSONS

rni/ukc\ ( Fernando Alvarez

Pteridophytes: Pteridophytes are vascular cryptogams. They are the earliest know vascular plants which originated in the Silurian period of

Post-doc fellowships to non-eu researchers FINAL REPORT. Home Institute: Centro de Investigaciones Marinas, Universidad de La Habana, CUBA

Transcription:

Phytotaxa 272 (2): 141 148 http://www.mapress.com/j/pt/ ISSN 1179-3155 (print edition) Copyright 2016 Magnolia Press Article PHYTOTAXA ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.272.2.5 Two New Species of Isoetes (Isoetaceae) from northern Brazil JOVANI B. DE S. PEREIRA 1, ALEXANDRE SALINO 2, ANDRÉ ARRUDA 3 & THOMAS STÜTZEL 4 1 Ruhr-Universität Bochum, Lehrstuhl für Evolution und Biodiversität der Pflanzen, 44780 Bochum, Germany. E-mail: Jovani.Pereira@rub.de 2 Universidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Depto de Botânica, Caixa Postal 486, CEP 30123 970, Belo Horizonte, Minas Gerais, Brazil. E-mail: salinobh@gmail.com 3 Universidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Depto de Botânica, Caixa Postal 486, CEP 30123 970, Belo Horizonte, Minas Gerais, Brazil. E-mail: ajarruda@gmail.com 4 Ruhr-Universität Bochum, Lehrstuhl für Evolution und Biodiversität der Pflanzen, 44780 Bochum, Germany. E-mail: thomas.stuetzel@rub.de Abstract Isoetes serracarajensis and I. cangae, two new species from northern Brazil, are described, illustrated, and compared to similar species. Isoetes serracarajensis can be distinguished from other species by a set of characters including triangular to linear microphylls, a reniform-orbicular labium, a rudimentary velum covering up to 1/5 of the sporangial surface, dark brown to red-brown sporangia and verrucate megaspores (verrucae type 1). Isoetes cangae presents large microphylls, a reniform-orbicular labium, a rudimentary velum covering only up to 1/4 of the sporangium surface, hyaline sporangia and verrucate (verrucae type 2) to tuberculate megaspores (tubercles type 3). Based on the IUCN criteria, we suggest that Isoetes serracarajensis should be classified as vulnerable (VU) and Isoetes cangae included as critically endangered (CR). Key words: aquatic plants, lycopsid, Serra do Carajás, spores, taxonomy Introduction The lycopsid genus Isoetes Linnaeus (1753: 1100) is a worldwide distributed plant group occurring aquatic in lakes, ponds, streams, estuaries, bogs, or terrestrial on seasonally inundated soil (Taylor & Hickey 1992). The genus comprises ca. 200 species, and South America is considered a center of both morphological and taxonomical diversity for Isoetes (Hickey 1990). Particularly in Brazil, the genus seems to be highly diverse with nearly 23 species (Prado et al. 2015). Efforts to understand the taxonomy of Isoetes from Brazil recently led authors to publish studies on spores (Lorscheitter et al. 2009), on chromosome numbers (Pereira et al. 2015), as well as on new species (Pereira et al. 2012, Pereira & Labiak 2013, Windisch et al. 2014). However, most of these studies were based on southeastern Brazilian taxa, where the genus seems to be more diverse (Prado et al. 2015). Meanwhile the genus is almost unknown from northern Brazil. Fieldworks conducted to access the ferns and lycophytes diversity in Brazilian Amazon resulted in the collection of two Isoetes species that we recognize as new to science. In this work, we provide descriptions, illustrations, images of the spores, and a taxonomic key to identify these new species. Material and Methods Materials of two new Isoetes species were collected in the Serra dos Carajás, Pará, northern Brazil (Fig. 5). Voucher specimens were deposited at B, BHCB and UPCB (acronyms following Thiers 2016). For each locality where these species were collected (see additional specimens examined), we examined spores of at least three specimens. To delimitate these two new species, we also compared them with the original descriptions and type-specimens of Isoetes Accepted by Marcus Lehnert: 7 August. 2016; published: 29 August. 2016 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 141

amazonica A. Braun (Spruce 1081, K, M), I. gardneriana Kunze ex A. Braun (Gardner 3563, B, K, E), I. ovata N. Pfeiff. (Goebel s.n., NY), and I. triangular U. Weber (Ule 8000, B, K). Spore images were generated by transferring the spores to aluminum scanning electron microscope (SEM) stubs coated with a carbon adhesive. The stubs were then coated with gold-palladium-alloy in a sputter-coater for 180 sec, after which the spores were digitally imaged using a Zeiss SIGMA VP. The resulting images were adjusted in Photoshop for contrast and the background was altered to black. To estimate the average measurements of the spores, we used a minimum of 20 spores per sporangium, from at least three sporangia. The terminology used for description of the spores follows that of Punt et al. (2007), with some slight modifications. For the macrosculpture of the megaspore surface, we define verrucae as distinct from tubercles by being broader than high (vs. tubercles are higher than broad). Based on analyses of the megaspores of the type materials of the more similar species (data not shown), the tubercles were classified into three types and the verrucae shown two types (Fig. 1). FIGURE 1. Macrosculptural elements on the megaspore surface of Isoetes. A. Isoetes ovata and I. triangula: tubercle type 1. B. Isoetes serracarajensis (only distal surface): tubercle type 2. C. Isoetes gardneriana and I. cangae: tubercle type 3. D. Isoetes serracarajensis and I. amazonica: verruca type 1. E. Isoetes cangae: verruca type 2. Taxonomy Isoetes serracarajensis J.B.S.Pereira, Salino & Stützel, sp. nov. (Figs. 2A D, 3) Isoetes serracarajensis is distinguished from other species of the Amazon Basin by a combination of the following characters: microphylls triangular to linear, labium reniform-orbicular, velum rudimentary to covering up to 1/5 of the sporangial surface, sporangium dark brown to red-brown on adaxial surface, megaspores verrucate (verruca type 1), with the laesures wider than higher or as wide as high and clearly separated from the remaining macrosculptural elements of the proximal surface. Type: BRAZIL. Pará: Parauapebas; Serra Norte, N6, 06 07 48 S, 50 10 32 W, 694 m, 26 January 2013, A.J. Arruda 1356 with P.L. Viana, M.O. Pivari, B.P. Leles, F. M. Santos (holotype B!, isotype BHCB!). Plants aquatic, submerged, growing in lakes and ponds. Corm globose, 0.4 0.8 cm wide, 3 lobate. Roots conspicuous, dichotomously branched. Leaves 1.0 1.5 mm wide at middle, 4 8( 14) cm long, 14 70 per individual, triangular to linear, straight, erect to ascending, apex acute to attenuate; alae 1.3 1.5 cm long, stretching along ca. 1/4 the length of the leaf, 1.5 2 mm wide at sporangium, hyaline, membranaceous, apex attenuate; subula present, olive green. Labium present, 1.0 2.2 mm wide, 0.8 1.2 mm long, reniform-orbicular. Ligule consisting of a thin membrane, generally not visible in dry material. Velum rudimentary to covering up to 1/5 of the adaxial sporangial surface, 0.2 0.4 mm along the lateral edges, 0.1 0.2 mm along the upper edges of the sporangium. Scales absent. Sporangium 2.2 4.7 mm long, 1.7 3.3 mm wide, elliptic, dark brown to red-brown, at the base of the leaf. Megaspore 470 640 µm diameter (x=490, N=20), 440 570 µm polar axis, 0.83 0.92 P/E ratio, subspheroidal, trilete, white, no lustrous, heteropolar; laesures 50 59 µm wide, 50 55 µm high, distinct, straight, wider than high or as wide as high, with straight and parallel sides, apex rounded to truncate, no apiculate, the same height along the whole length, slightly separated from the remaining macrosculptural elements; proximal surface macrosculpture verrucate, verrucae type 1 (rarely tubercles type 2), 23 42 µm wide, 10.0 20.0 µm high, microsculpture foveolate with microechinae; equatorial ridges distinct, straight, with straight and paralell sides, apex rounded to truncate; distal surface macrosculpture verrucate, verrucae type 1, 23 42 µm wide, 13.0 23.0 µm high, microsculpture foveolate with microechinae. Microspore 30 36 µm long (x=34, N=20), light brown to dark brown, monolete, heteropolar; laesure straight, without prominent invagination; proximal surface macrosculpture psilate (rarely with minute echinae), microsculpture comprising microgranula and microbacula; distal surface macrosculpture echinate to tuberculate, microsculpture comprising microgranula and microbacula. Etymology: The specific epithet refers to the localities where this species was collected, Serra do Carajás, located in southern Pará, Brazil. 142 Phytotaxa 272 (2) 2016 Magnolia Press Pereira et al.

FIGURE 2. Habitat of the holotypes. A D. Isoetes serracarajensis (Arruda 1356 ). A B. Habitat. C. Adaxial view of the base of the microphylls with velum covering less than 1/5 of the sporangial surface. D. Diagram of the adaxial view of the microphylls showing the ligula position, labium, velum and sporangium. E H. Isoetes cangae (Arruda 1329 ). E F. Habitat. G. Adaxial view of the base of the microphylls with velum covering less than 1/4 of the sporangial surface. H. Diagram of the adaxial view of the microphylls showing the ligula position, labium, velum and sporangium. Scale bars: A, B, E and F = 1 cm; C D = 1 mm; G H= 2 mm. Isoetes from northern Brazil Phytotaxa 272 (2) 2016 Magnolia Press 143

Additional specimens examined (paratypes): BRAZIL. Pará: Parauapebas, Serra Norte, N7, 06 09 13 S, 50 10 21 W, 692 m, 25 March 2012, A.J. Arruda et al. 854 (B, BHCB). Canaã dos Carajás: Serra Sul, 06 21 7 S, 50 23 44 W, 735 m, 23 January 2013, A.J. Arruda et al. 1338 (B, BHCB); Floresta Nacional de Carajás, Serra Sul, Corpo B, 06 21 06 S, 50 23 43 W, 733 m, 14 February 2010, T.E. Almeida 2157 (BHCB, UPCB); Floresta Nacional de Carajás, Serra Sul, 06 24 32 S, 50 21 04 W, 822 m, 9 December 2014, V. Giorni & P. Burkowski s.n. (B, BHCB); Floresta Nacional de Carajás, Serra Sul, 06 24 10 S, 50 18 24 W, 655 m, 16 March 2015, V. Giorni s.n. (BHCB, UPCB); Floresta Nacional de Carajás, Serra Sul, 06 22 00 S, 50 23 43 W, 733 m, 17 March 2015, V. Giorni s.n. (B, BHCB). FIGURE 3. SEM images of the spores of Isoetes serracarajensis (from the holotype). A F. Verrucate megaspore. A. Proximal view. B. Distal view. C. Equatorial view. D. Detail of the proximal surface. E. Detail of the distal view. F. Detail of the verruca of the distal view. G I. Microspore. G. Distal view showing the echinate-tuberculate macrosculpture. Lateral view. H. Proximal view showing the psilate macrosculpture. I. Detail of the surface of the microspore. Scale bars: A C = 100 µm; D E = 20 µm; F H = 2 µm; I = 1 µm. Comments: Three species of Isoetes with tuberculate or verrucate megaspores occur in the Amazon Basin: Isoetes amazonica Braun in Baker (1880: 109), I. ovata Pfeiffer (1922: 108) and I. triangula Weber (1922: 253). Among these, I. amazonica is more similar to I. serracarajensis by its microphyll size and verrucate megaspore. However, in I. amazonica the microphylls are acicular to filiform, 0.4 0.8 mm wide at middle (vs. triangular to linear microphylls, 1.0 1.5 mm wide at middle), the adaxial surface of the sporangia is hyaline (vs. dark brown to red-brown), the laesures of the megaspore presents convex sides and obtuse apices (vs. parallel sides and rounded to truncate apex), and the macrosculptural elements of the proximal surface are connected to laesures (vs. macrosculptural elements clearly separated from laesures). 144 Phytotaxa 272 (2) 2016 Magnolia Press Pereira et al.

Distribution and Habitat: Isoetes serracarajensis is only known from four localities (Serra Norte, Serra Sul, Serra do Tarzan, and Serra do Bocaína), that form the mountain range Serra dos Carajás (Fig. 5). It was found narrowly associated to canga vegetation and submerged in seasonal lakes, ponds, or terrestrial on wet soil on top of the mountains at 650 822 m. Conservation Status: This species is recorded from areas in which the soils present high iron contents. The increase of the iron exploration in these localities by mining companies has led to deterioration of the quality of the habitats of Isoetes serracarajensis and several subpopulations may have already been extinct. Licensing processes for the construction of new iron mines have been initiated and therefore, a continuing decline of the populations is expected. Based on the IUCN criteria (IUCN 2012), 2010), we suggest that I. serracarajensis should be classified as Vulnerable (VU). FIGURE 4. SEM images of the spores of Isoetes cangae (from the holotype). A F. Verrucate-tuberculate megaspore. A. Proximal view. B. Distal view. C. Equatorial view. D. Detail of the proximal surface. E. Detail of the distal view. F. Detail of the verruca of the distal view. G I. Microspore. G. Distal view showing the echinate-tuberculate macrosculpture. H. Proximal view showing the inconspicuously echinate macrosculpture. I. Detail of the surface of the microspore. Scale bars: A C = 100 µm; D E = 20 µm; F = 2 µm; G and H = 9 µm; I = 1 µm. Isoetes cangae J.B.S.Pereira, Salino & Stützel, sp. nov. Isoetes cangae is distinguished from other species of the Amazon Basin by the combination of the following characters: microphylls large (15 30 cm long), labium reniform-orbicular, velum rudimentary to covering up to 1/4 of the sporangium surface, sporangium hyaline, megaspore white, verrucate (verrucae type 2) to tuberculate (tubercles type 3) (Figs. 2E H, 4). Isoetes from northern Brazil Phytotaxa 272 (2) 2016 Magnolia Press 145

Type: BRAZIL. Pará: Canaã dos Carajás, Serra Sul, S11D, 06 23 57 S, 50 22 13 W, 730 m, 22 January 2013, A.J. Arruda 1329, M.O. Pivari, B.P. Leles, F.M. Santos (holotype B!; isotype BHCB!). Plants aquatic, submerged, growing among rocks in lakes. Corm globose, 0,8 1.3 cm wide, 3 lobate. Roots conspicuous, dichotomously branched. Leaves 0.65 1.2 mm wide at middle, 15 25 cm long, 25 50 per individual, linear, straight, ascending, apex acute; alae 2.5 4.0 cm long, stretching along ca. 1/5 the length of the leaf, 1.5 2.5 mm wide at sporangium, hyaline to light green, membranaceous, apex acuminate; subula present, olive-green. Labium present, 2.6 3.5 mm wide, 1.8 2.4 mm long, reniform-orbicular. Ligule a thin membrane, generally not visible in dry material. Velum rudimentary to covering less than 1/4 of the adaxial sporangial surface, 0.1 0.4 mm along the lateral edges, and 0.1 0.26 mm along the upper edges of the sporangium. Scales absent. Sporagium 2.2 3.0 mm wide, 3.3 4.5 mm long, elliptic, light brown, at the basal of the leaf. Megaspores 490 580 µm diameter (x=510, N=20), 440 510 µm polar axis, 0.88 0.96 P/E ratio, subspheroidal, trilete, white, slightly lustrous, heteropolar; laesures 31 35 µm wide, 40 52 µm high, distinct, straight, higher than wide, with straight and inclined sides, apex acute to obtuse, not apiculate, the same height along the whole length, slightly separated from the remaining macrosculptural elements; proximal surface macrosculpture verrucate to tuberculate, tubercles type 3 and verrucae type 2, 13 32 µm wide, 10 22 µm high, microsculpture foveolate with microechinae and microgranula; equatorial ridges distinct, straight, with convex sides, apex rounded; distal surface macrosculpture verrucate to tuberculate, tubercles type 3 and verrucae type 2, 15 35 µm wide, 15.0 23.0 µm high, microsculpture foveolate with microgranula and microechinae. Microspores 29 34 µm long (x=31.5, N=20), light brown, monolete, heteropolar; laesure straight, without prominent invagination; proximal surface macrosculpture inconspicuously echinate, microsculpture comprising microgranula and microbacula; distal surface macrosculpture echinate to tuberculate, microsculpture comprising microgranula and microbacula. FIGURE 5. Serra dos Carajás comprising its four mountain chains (Serra Norte, Serra Sul, Serra do Tarzan and Serra do Bocaína), in the southern part of the Pará State, northern Brazil. White line marks the limits of the Carajás National Park. Type locality of I. serracarajensis in Serra Norte. Type locality of I. cangae in Serra Sul. Etymology: The specific epithet refers to the canga, a superficial iron crust which occurs over ferriferous formations, where Isoetes cangae was found. 146 Phytotaxa 272 (2) 2016 Magnolia Press Pereira et al.

Comments: Isoetes gardneriana Braun (1862: 330) is similar to I. cangae in microphyll size, having tuberculate megaspores (tubercles type 3) and a velum covering less than 1/4 of the adaxial sporangial surface. However, in Isoetes gardneriana the megaspores are dark brown to grey (vs. white), the laesures are knife-like (vs. sharply triangular), and the distal surface of the microspores is laevigate to papillate (vs. echinate to tuberculate). Distribution and Habitat: Isoetes cangae is only known from its type locality in Serra Sul, Canaã dos Carajás, located in southern Pará, Brazil (Fig. 5). It was found submerged in permanent lakes over canga soil, in rupestrian fields at 730 m. Conservation Status: Although innumerous efforts have been made to find new populations of I. cangae in the Serra dos Carajás, this species is currently known from a single locality, and only from a few individuals. Isoetes cangae is recorded in an area, which is surrounded by iron mines. The increase of the mining operations in this locality has led to deterioration of the quality of the habitats of I. cangae and populations may have already been extinct. Licensing processes for the amplification of iron mines have been initiated and therefore, a drastic decline of this species is expected. Based on the IUCN criteria (IUCN 2012), we suggest that I. cangae should be classified as critically endangered (CR). Key to species of Isoetes with tuberculate and verrucate megaspores from the Amazon Basin 1. Leaves longer than 15 cm...2. Leaves up to 14 cm...6 2. Megaspores 750 900 µm diam... I. ovata. Megaspores 350 700 µm diam...3 3. Laesures of the megaspores with apex attenuate, acute or obtuse...4. Laesures of the megaspores with apex truncate to rounded...5 4. Megaspores dark brown, laesures knife-like; microspore papillate; plants from midwestern Brazil (Goiás State)... I. gardneriana. Megaspores white, laesures sharply triangular (straight inclined sides with apex acute); distal surface of the microspore echinate to tuberculate; plants from northern Brazil (Pará State)...I. cangae 5. Megaspores oblate (P/E ratio=0.54 0.75), macrosculptural elements with apex rounded (tubercles type 1)... I. triangula. Megaspores subspheroidal (P/E ratio=0.83 0.92), macrosculptural elements with apex truncate (verrucae type 1, or rarely, tubercles type 2)... I. serracarajensis 6. Leaves filiform, 0.4 0.8 mm wide; sporangia hyaline; proximal view of the megaspore without distinct separation between the laesures and tubercles), laesures with convex sides and obtuse apex...i. amazonica. Leaves triangular-linear, 1.0 1.5 mm wide; sporangia dark brown to red brown; proximal view of megaspores with distinct separation between laesures and macrosculptural elements, laesures with parallel sides and rounded to truncate apex...... I. serracarajensis Acknowledgments The authors thank the curators and collection managers of the herbaria B, BHCB, E, K, M, NY, US and UPCB for specimen loans and access to their collections. We are also grateful to Thaís Almeida by providing the maps of Serra Carajás, CAPES for the scholarship to A.J. Arruda, CNPq for research fellowship grant to A. Salino (Proc. 306868/2014-8). This study is part of Jovani Pereira s PhD Dissertation, which was made possible through a fellowship from CNPq (Proc. 245951/2012-1). References Baker, J.G. (1880) A synopsis of the species of Isoetes. Journal of Botany, British and Foreign 9: 65 110. Braun, A. (1862) Zwei deutsche Isoëtes-Arten nebst Winken zur Aufsuchung derselben. Verhandlungen des botanischen Vereins für die Provinz Brandenburg und die angrenzenden Länder 4: 299 333. Hickey, R.J. (1990) Studies of Neotropical Isoëtes L. I. Euphyllum, a new subgenus. Annals of the Missouri Botanical Garden 77: 239 245. http://dx.doi.org/10.2307/2399537 IUCN (2012) The IUCN red list categories and criteria, version 3.1. IUCN Red List Unit, Gland, Switzerland and Cambridge, UK. Available from: http://www.iucnredlist.org/technical-documents/categories-and-criteria (accessed 4 February 2016) Isoetes from northern Brazil Phytotaxa 272 (2) 2016 Magnolia Press 147

Linnaeus, C. (1753) Species Plantarum 2. L. Salvius, Stockholm, 1200 pp. Lorscheitter, M.L., Ashraf, A.R., Windisch, P.G. & Mosbrugger, V. (2009) Pteridophyte spores of Rio Grande do Sul flora, Brazil. Palaeontographica 281: 1 96. Pereira, J.B.S., Windisch, P.G., Lorscheitter, M.L. & Labiak, P.H. (2012) Isoetes mourabaptistae, a new species from Southern Brazil. American Fern Journal 102: 174 180. http://dx.doi.org/10.1640/0002-8444-102.2.174 Pereira, J.B.S. & Labiak, P.H. (2013) A new species of Isoetes with tuberculate spores from Southeastern Brazil (Isoetaceae). Systematic Botany 38: 869 874. http://dx.doi.org/10.1600/036364413x674742 Pereira, J.B.S., Mittelbach, M. & Labiak, P.H. (2015) Studies on chromosome numbers and spore size in Brazilian Isoetes. American Fern Journal 105: 226 237. http://dx.doi.org/10.1640/0002-8444-105.3.226 Pfeiffer, N.E. (1922) Monograph of the Isoetaceae. Annals of the Missouri Botanical Garden 9: 79 233. http://dx.doi.org/10.2307/2990000 Prado, J., Sylvestre, L.S., Labiak, P.H., Windisch, P.G., Salino, A., Barros, I.C.L., Hirai, R.Y., Almeida, T.E., Santiago, A.C.P., Kieling- Rubio, M.A., Pereira, A.F. de N., Øllgaard, B., Ramos, C.G.V., Mickel, J.T., Dittrich, V.A.O., Mynssen, C.M., Schwartsburd, P.B., Condack, J.P.S., Pereira, J.B.S. & Matos, F.B. (2015) Diversity of ferns and lycophytes in Brazil. Rodriguésia 66: 1073 1083. http://dx.doi.org/10.1590/2175-7860201566410 Punt, W., Hoen, P.P., Blackmore, S., Nilsson, S. & Le Thomas, A. (2007) Glossary of pollen and spore terminology. Review of Palaeobotany and Palynology 143: 1 81. http://dx.doi.org/10.1016/j.revpalbo.2006.06.008 Taylor, C.W. & Hickey, R.J. (1992) Habitat, evolution, and speciation in Isoëtes. Annals of the Missouri Botanical Garden 79: 613 622. http://dx.doi.org/10.2307/2399755 Thiers, B. (2016, 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 1 August 2016) Weber, U. (1922) Zur Anatomie und Systematik der Gattung Isoëtes L. Hedwigia 63: 219 262. Weber, U. (1934) Neue südamerikanische Isoëtes-Arten. Berichte der Deutschen Botanischen Gesellschaft 52: 121 125. Windisch, P.G., Lorscheitter, M.L. & Nervo, M.H. (2014) Isoetes naipiana (Isoetaceae), a new species from southern Brazil. Willdenowia 44: 393 398. http://dx.doi.org/10.3372/wi.44.44309 148 Phytotaxa 272 (2) 2016 Magnolia Press Pereira et al.