<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0370-3908</journal-id>
<journal-title><![CDATA[Revista de la Academia Colombiana de Ciencias Exactas, Físicas y Naturales]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. acad. colomb. cienc. exact. fis. nat.]]></abbrev-journal-title>
<issn>0370-3908</issn>
<publisher>
<publisher-name><![CDATA[Academia Colombiana de Ciencias Exactas, Físicas y Naturales]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0370-39082016000400012</article-id>
<article-id pub-id-type="doi">10.18257/raccefyn.403</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Novelties in Rapatea (Rapateaceae) from Colombia]]></article-title>
<article-title xml:lang="es"><![CDATA[Novedades en Rapatea (Rapateaceae) para Colombia]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[C.]]></surname>
<given-names><![CDATA[Gerardo A. Aymard]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Arellano-Peña]]></surname>
<given-names><![CDATA[Henry]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,UNELLEZ-Guanare Programa de Ciencias del Agro y el Mar Herbario Universitario (PORT)]]></institution>
<addr-line><![CDATA[Mesa de Cavacas Estado Portuguesa]]></addr-line>
<country>Venezuela</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidad Nacional de Colombia Instituto de Ciencias Naturales Grupo de Investigación en Biodiversidad y Conservación]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>01</day>
<month>12</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>01</day>
<month>12</month>
<year>2016</year>
</pub-date>
<volume>40</volume>
<numero>157</numero>
<fpage>644</fpage>
<lpage>652</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0370-39082016000400012&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0370-39082016000400012&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0370-39082016000400012&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Rapatea isanae, from the upper Isana &#91;Içana&#93; river, Guianía Department, Colombia, is described and illustrated, and its morphological relationships with allied species are discussed. This taxon is remarkable for Rapatea in its small stature (15-30 cm tall) and leaves, and it is only the second species with white petals in a genus that otherwise has only yellow petals. It is most closely R. spruceana, with the base of the leaf blade gradually tapering from the intergrading into the petiole, and the bractlet of the spikelet and sepal shape. However, this new species differs from R. spruceana in its shorter size, sparse verrucose on the lower surface, the length of the attenuate portion of the involucral bracts, and the shape and color of the petals. It also has similarities to R. longipes and R. modesta in its ventricose sheath-leaf, inflorescence shape, and bractlets equal in length. A previously described species from Colombia is restablished (i.e., R. modesta), and one variety is elevated to the rank of species (i.e., R. paludosa var. sessiliflora to R. sessiliflora). An updated key to the all twenty five species of Rapatea, and an abstract in Kuripaco are also provided.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Rapatea isanae, una nueva especie del alto río Isana, Departamento del Guianía, Colombia, es descrita, ilustrada, y sus relaciones morfológicas con las especies afines son discutidas. Esta especie es notable en el género Rapatea por el tamaño de las plantas (entre 15 y 30 cm de altura), las hojas muy pequeñas, y los pétalos blancos, siendo la segunda especie con este carácter en un género en el cual predominan los pétalos amarillos. Por la base de las hojas transformándose gradualmente en un pecíolo, la morfología de las bractéolas de las espiguillas y los sépalos, R. isanae está relacionada con R. spruceana. Por las vainas basales de las hojas ventricosas, la forma convexa de las inflorescencias y las bractéolas del mismo tamaño con R. longipes y R. modesta, respectivamente. Sin embargo, esta nueva especie difiere de R. spruceana por ser plantas muy pequeñas, el envés esparcidamente verrugoso, el largo de la porción atenuada de las brácteas involúcrales y la forma y color de los pétalos. Se restablece una especie previamente descrita para Colombia (i.e., R. modesta), y una variedad es elevada al rango de especie (i.e., R. paludosa var. sessiliflora a R. sessiliflora). Adicionalmente se presenta una clave actualizada de las 25 especies aceptadas de Rapatea y un resumen en Kuripaco.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Rapatea]]></kwd>
<kwd lng="en"><![CDATA[sect. Longipes]]></kwd>
<kwd lng="en"><![CDATA[Colombia]]></kwd>
<kwd lng="en"><![CDATA[Isana -{Içana}- river]]></kwd>
<kwd lng="en"><![CDATA[upper Rio Negro]]></kwd>
<kwd lng="en"><![CDATA[Rapateaceae]]></kwd>
<kwd lng="es"><![CDATA[Rapatea]]></kwd>
<kwd lng="es"><![CDATA[sect. Longipes]]></kwd>
<kwd lng="es"><![CDATA[Río Isana -{Içana}-]]></kwd>
<kwd lng="es"><![CDATA[Alto Río Negro]]></kwd>
<kwd lng="es"><![CDATA[Colombia]]></kwd>
<kwd lng="es"><![CDATA[Rapateaceae]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  <font face="verdana" size="2"> &nbsp;    <p>doi: <a href="http://dx.doi.org/10.18257/raccefyn.403">http://dx.doi.org/10.18257/raccefyn.403</a></p> &nbsp;    <p><font size="4">    <center> <b>Novelties in <i>Rapatea</i><i> </i>(Rapateaceae)   from Colombia</b> </center></font></p> &nbsp;    <p><font size="3">    <center> <b>Novedades en <i>Rapatea</i><i> </i>(Rapateaceae) para Colombia</b> </center></font></p> &nbsp;    <p>    <center> <b>Gerardo A. Aymard C.<sup>1,2,</sup>*,   Henry Arellano-Pe&ntilde;a<sup>1,3</sup></b> </center></p>     <p><sup>1</sup> Compensation International Progress S. A. -Ciprogress Greenlife-, Bogot&aacute;,   Colombia    <br> <sup>2</sup> UNELLEZ-Guanare,   Programa de Ciencias del Agro y el Mar, Herbario Universitario (PORT), Mesa de Cavacas, Estado Portuguesa, Venezuela     ]]></body>
<body><![CDATA[<br> <sup>3</sup> Grupo   de Investigaci&oacute;n en Biodiversidad y Conservaci&oacute;n, Instituto de Ciencias   Naturales, Universidad Nacional de Colombia, Bogot&aacute;, Colombia</p> <hr size="1">     <p><b>Abstract</b></p>     <p><i>Rapatea</i><i> isanae</i>, from the   upper Isana &#91;I&ccedil;ana&#93; river, Guian&iacute;a Department, Colombia, is described and illustrated,   and its morphological relationships with allied species are discussed. This   taxon is remarkable for <i>Rapatea</i><i> </i>in its   small stature (15-30 cm tall) and leaves, and it is   only the second species with white petals in a genus that otherwise has only   yellow petals. It is most closely <i>R. spruceana</i>,   with the base of the leaf blade gradually tapering from the intergrading into   the petiole, and the bractlet of the spikelet and   sepal shape. However, this new species differs from <i>R. spruceana </i>in its shorter size, sparse verrucose on the   lower surface, the length of the attenuate portion of the involucral bracts, and the shape and color of the petals. It also has similarities to <i>R. longipes </i>and <i>R. modesta </i>in its ventricose sheath-leaf, inflorescence   shape, and bractlets equal in length. A previously   described species from Colombia is restablished (i.e., <i>R. modesta</i>), and one variety is   elevated to the rank of species (i.e., <i>R. paludosa </i>var. <i>sessiliflora</i><i> </i>to <i>R. sessiliflora</i>). An updated key to the all twenty five   species of <i>Rapatea</i>, and an abstract in Kuripaco are also provided. </p>     <p><b>Key   words: </b><i>Rapatea</i><i>; </i>sect. <i>Longipes</i><i>; </i>Colombia; Isana &#91;I&ccedil;ana&#93; river; upper Rio Negro; Rapateaceae.</p> <hr size="1">     <p><b>Resumen</b></p>     <p><i>Rapatea</i><i> isanae</i>, una nueva especie   del alto r&iacute;o Isana, Departamento del Guian&iacute;a, Colombia, es descrita, ilustrada, y sus relaciones   morfol&oacute;gicas con las especies afines son discutidas. Esta especie es notable en   el g&eacute;nero <i>Rapatea</i><i> </i>por el tama&ntilde;o de las   plantas (entre 15 y 30 cm de altura), las hojas muy peque&ntilde;as, y los p&eacute;talos   blancos, siendo la segunda especie con este car&aacute;cter en un g&eacute;nero en el cual   predominan los p&eacute;talos amarillos. Por la base de las hojas transform&aacute;ndose   gradualmente en un pec&iacute;olo, la morfolog&iacute;a de las bract&eacute;olas de las espiguillas   y los s&eacute;palos, <i>R. isanae </i>est&aacute; relacionada con <i>R. spruceana</i>. Por las vainas basales de las hojas ventricosas, la forma convexa de las inflorescencias y las   bract&eacute;olas del mismo tama&ntilde;o con <i>R. longipes </i>y <i>R.     modesta</i>, respectivamente. Sin embargo, esta nueva especie difiere de <i>R. spruceana </i>por ser plantas muy peque&ntilde;as, el env&eacute;s   esparcidamente verrugoso, el largo de la porci&oacute;n atenuada de las br&aacute;cteas invol&uacute;crales y la forma y color de los p&eacute;talos. Se   restablece una especie previamente descrita para Colombia (i.e., <i>R. modesta</i>),   y una variedad es elevada al rango de especie (i.e., <i>R. paludosa </i>var. <i>sessiliflora</i><i> </i>a <i>R. sessiliflora</i>). Adicionalmente se   presenta una clave actualizada de las 25 especies aceptadas de <i>Rapatea</i><i> </i>y un resumen en Kuripaco. </p>     <p><b>Palabras clave: </b><i>Rapatea</i><i>; </i>sect. <i>Longipes</i><i>; </i>R&iacute;o Isana &#91;I&ccedil;ana&#93;; Alto   R&iacute;o Negro; Colombia; Rapateaceae.</p> <hr size="1">     <p>Abstract in Kuripaco. Supplementary   information 1, <a href="http://www.raccefyn.co/index.php/raccefyn/article/downloadSuppFile/403/1749" target="_blank">http://www.raccefyn.co/index.php/raccefyn/article/downloadSuppFile/403/1749</a></p> <hr size="1"> &nbsp;    <p><font size="3"><b>Introduction</b></font></p>     <p><i>Rapatea</i><i> </i>Aubl. is the most widely distributed genus in the Rapateaceae (<b>Boom</b>, 1994). It currently comprises   about 25 species of terrestrial herbs from 15 cm to 2 m tall, occurring in   Panama, Colombia, Venezuela, Trinidad, Guyana, Suriname, French Guiana,   Ecuador, Peru, Brazil and Bolivia (<b>Monteiro</b>,   2011). Species of <i>Rapatea</i><i> </i>occur along   streams, in the edges and shady understory of flooded (<b>Rangel-Ch.</b>, 2008)   and terra firme forests, riparian granitic outcrops (<b>Giraldo-Ca&ntilde;as</b>, 2008), and in the oligotrophic,   seasonal flooded white-sand savannas associated with black-water rivers (<b>Berry</b>,   2004; <b>Huber, </b>2005; 2006). Like the rest of the family, most of the   species of <i>Rapatea</i><i> </i>have radiated   successfully in the Amazon basin and on the Guiana Shield (<b>Ducke</b>,   1938; <b>Berry <i>et al</i></b><i>.</i>, 1995; <b>Givnish</b><b> <i>et al.</i></b>, 2000, 2004; <b>Bouchenak-Khelladi</b><b> <i>et al</i>., </b>2014; <b>Fern&aacute;ndez</b><b>-L. <i>et     al</i>., </b>2016). Few species are found outside of this region, such as <i>R. paludosa </i>Aubl., the   most widespread species of the genus (from Panama, Trinidad, and Venezuela to   Bahia state in Brazil). Furthemore, <i>Rapatea</i><i> pycnocephala </i>Seub. is known in central and southeastern Brazil (Mato Grosso do Sul: Xavantina; Bahia), and <i>R. spectabilis </i>Pilg. has   been collected south to southern in Bolivia (Beni); <i>R. elongata </i>G. K. Schultze is common in northeastern of Colombia, an area that harbors some of the wettest   forests in the world (<b>Arellano-Pe&ntilde;a &amp; Rangel-Ch.</b>, 2004). This region   is known as the biogeographical Choc&oacute; or &quot;Choc&oacute; biogeogr&aacute;fico&quot;, and it is a broad strip of land with the   highest biodiversity found between the Pacific Ocean and the slopes of the   Western Cordillera (<b>Cuatrecasas</b><b>, </b>1989; <b>Rangel-Ch., </b>2004). <i>Rapatea</i><i> </i>is rare in the   Andes, however two populations of <i>R. muaju </i>Garc&iacute;a-Barr. &amp; L. E. Mora had been detected in Ecuador   from collections made in the last 25 years in the foothills (&quot;Piedemonte Andino&quot;), the lower   mountains (380-930 m) of Morona-Santiago Department, (see: <a href="http://www.tropicos.org/Name/27200122?tab=specimens" target="_blank">http://www.tropicos.org/Name/27200122?tab=specimens</a>),   and in &quot;Cerro Kaputna&quot; in the Cordillera del C&oacute;ndor (<b>Neill, <i>et al., </i></b>2007). This region   forms part of the &quot;sub-Andean cordillera&quot; made up principally of Mesozoic and   early Tertiary sediments of sandstones and limestones (<b>Rodr&iacute;guez-R., <i>et al., </i></b>2013) that form the border between Ecuador   and Peru. The vegetation of these Cordillera have a phytogeographical connection with the Guayana Shield in northeastern   South America (<b>Neill, </b>2005). As a consequence, an important number of   plant genera once thought to be endemic to the sandstone mountains (Tepuis) of the Guayana region   have been found to occur disjunctly on the sandstone   portions of the Andean cordilleras, but not elsewhere in the Andean region (<b>Berry     &amp; Riina</b>, 2005; <b>Aymard</b><b> &amp; Campbell</b>, 2008). </p>     ]]></body>
<body><![CDATA[<p><i>Rapatea</i><i> </i>is distinguished from other genera in the family by its   laterally compressed inflorescences, which are subtended by two conspicuous involucral bracts that contain a capitate or elongate assemblage of flowers (<b>Stevenson, <i>et al., </i></b>1998; <b>Stevenson</b>,   2004). The anthers are tipped with a cochleariform appendage (<b>Oriani</b><b> &amp; Scatena</b>,   2013), and the carpels are uniovulate with basal   placentation, with seeds that are oblong and exappendiculate,   with longitudinal striations. A revision of the genus was published by <b>Maguire </b>(1965), who recognized 18 species and placed them in three sections (<i>Elongata</i><i>, Longipes, </i>and <i>Paludosa</i>). Maguire employed three characters   to separate the species: the base of leaf blades, the length of the bractlets of the spikelets, and   the shape of the inflorescence receptacle. Since then, four new species and two   varieties have been described (<b>Maguire</b>, 1979; <b>Steyermark</b>,   1988, <b>Steyermark</b><b>, <i>et al</i>.</b>, 1989; <b>Boom</b>,   1994). The genus has also been treated for &quot;Flora de Venezuela&quot; (<b>Maguire</b>,   1982), Flora of Ecuador (<b>Berry</b>, 1999), Flora of the Venezuelan Guayana (<b>Berry</b>, 2004), the checklist of the plants   of the Guiana Shield (<b>Berry</b>, 2007), and lately in the &quot;Cat&aacute;logo de Plantas y L&iacute;quenes de Colombia&quot; (<b>Berry</b>, 2016). </p>     <p>This new   species increases to 12 the number of <i>Rapatea</i><i> </i>species known from Colombia, and 25 for the genus. Five of these species   are restricted to the R&iacute;o Negro basin in the Amazonian region of Brazil,   Colombia and Venezuela (<i>R. angustifolia </i>Spruce   ex K&ouml;rn., <i>R. circasiana </i>Garc&iacute;a-Barr. &amp; L. E. Mora, <i>R. isanae </i>Aymard &amp; Arellano-Pe&ntilde;a, <i>R. longipes </i>Spruce ex K&ouml;rn., and <i>R. spruceana </i>K&ouml;rn.).   This region harbors an array of plant families species that tolerate the   nutrient-poor soils habitats derived by sandstone substrates such as the white   sand savannas surrounded by Amazonian Caatinga (&quot;Campinarana florestada&quot;), as well   as open areas like the Bana (&quot;Campinas&quot; in Brazil)   vegetation, most often found near black-water rivers (<b>Huber, </b>1988<b>; Kubitzki, </b>1989; 1990; <b>Berry &amp; Riina, </b>2005). </p>     <p><b>Taxonomy</b><b>. </b><i>Rapatea</i><i> isanae </i>Aymard &amp; Arellano-Pe&ntilde;a, <i>sp</i><i>. nov. </i>(<a href="#f1">Figures   1</a>, <a href="#f2">2</a>, <a href="#f3">3</a>, y <a href="#f4">4</a>). </p>     <p>    <center><a name="f1"><img src="img/revistas/racefn/v40n157/v40n157a12f1.gif"></a></center></p>     <p>    <center><a name="f2"><img src="img/revistas/racefn/v40n157/v40n157a12f2.jpg"></a></center></p>     <p>    <center><a name="f3"><img src="img/revistas/racefn/v40n157/v40n157a12f3.jpg"></a></center></p>     <p>    ]]></body>
<body><![CDATA[<center><a name="f4"><img src="img/revistas/racefn/v40n157/v40n157a12f4.jpg"></a></center></p>     <p><b>Type</b><b>: </b>COLOMBIA. Guian&iacute;a: Panapan&aacute;, Corregimiento   de Venado, alto r&iacute;o Isana, alrededores de la   Comunidad Punta Tigre, 1&deg; 4&#39; 25.5048&#39;&#39; N; 69&deg; 43&#39; 58.0296&#39;&#39; W, 185 m, 7 de Mayo   2014, <i>F. Castro-Lima, G. Aymard C., V. Minorta-C., H. Arellano-P., L. Ni&ntilde;o, A. Lozano, M. Gonz&aacute;lez     &amp; C. Villegas 18324 </i>(holotype: COL; isotype: COAH). </p>     <p><b>Diagnosis: </b><i>Rapatea</i><i> isanae </i>differs from the morphologically most similar species <i>R. spruceana </i>Spruce ex K&ouml;rn.   in its shorter stature (15-30 cm tall), leaf of the lamina is shorter (8-13 cm   long), the lower surface of the leaf sparse verrucose,   the involucral bracts covered by shorter glandular trichomes in the basal portion outside, the attenuate   portion 1-5 mm long, spikelets shortly pedicellate, bractlets not   ciliate at the margins, petals white, broadly obovate,   and the apical appendage of anthers brown. </p>     <p><b>Herb </b>acaulescent,   perennial, erect, 15-30 cm tall. <b>Leaves </b>3 to 15 per plant, leaf sheaths   reddish, glabrous, conduplicate, equitant and   distichous, subcoriaceous to chartaceous,   elongate, with about 50 distinct nerves, 5-9 cm long x 0.8-10 cm wide; base of   leaf blades gradually passing into the petiole, petioles slender, 1.5-10 cm   long, glabrous, narrowled toward the apex; <b><i>leaf     blades </i></b>subcoriaceous, lanceolate,   5-13 cm long x 1-1.3 cm wide, glabrous on both sides, sparsely verrucose along the veins on the lower surface, with 12-15   secondary veins, the base attenuate, the apex long-acuminate, acumen ca. 1 cm   long. <b>Inflorescence </b>1-3 per plant, peduncle 10-15 cm long, 1-1.5 mm   thick, glabrous, canaliculate, somewhat broadened and   medially compressed at the summit below the head, head compressed, broadly   ovate, subtended by 2 involucral bracts red ca. 1.5 x   ca. 1.5 cm, coriaceous, covered by short glandular trichomes on the basal portion outside, glabrous inside, multinerved (ca. 100 nerves), receptacle convex, ca. 5 mm x 5 mm, the attenuate apex of the involucral bracts 1-5 mm long, <b><i>spikelets</i></b><b><i> </i></b>12-15 per inflorescence, pedicels ca. 1 mm long, <b><i>bractlets</i></b><b><i> </i></b>18-20 per spikelet, linear-oblanceolate, 7-10   mm x ca. 1 mm, 3-nerved, membranaceous, glabrous on   both sides, shortly acuminate. <b>Flower: <i>sepals </i></b>coriaceous, lanceolate-acuminate, 3 or 4-veined, 4-6 mm x ca. 2 mm,   glabrous on both sides, bases membranous and basally connate into a tube 4-5 mm   long, upper halves free; <b><i>petals </i></b>white, blade widely-obovate, membranous, 8-11 mm x 5-6, shortly apiculate at the apex, margins erose,   7-10-veined, the basal claws ca. 3 mm long, connate for 1-2 mm at the base,   glabrous on both sides; <b><i>stamens </i></b>6, the filaments 1.5-2.4 mm long,   inserted near the base of the corolla tube, staminal tube ca. 3.5 mm long, anthers extrorse, white, 3-3.4   mm long with a brownish apical cochleariform linear-oblong appendage ca. 1.5 mm long, attached by a short, sigmoid base; <b><i>ovary </i></b>conical to subcapitate, ca. 2 mm x ca. 2 mm,   style equaling the stamens<b>, </b>9-10 mm long, the stigma curved, acute. <b>Fruits </b>and <b><i>seeds </i></b>not seen.</p>     <p><b>Distribution and habitat. </b>In the edges and in shaded places of oligotrophic,   flooded white-sand savannas from the upper Isana &#91;I&ccedil;ana&#93; river, Guian&iacute;a Department,   Colombia, at elevations of 185 m. </p>     <p><b>Taxonomic   notes. </b>Because of the spikelets bractlets of the of   equal length and the inflorescence receptacle convex or hemispheric, <i>Rapatea</i><i> isanae </i>belongs   to <i>Rapatea</i><i> </i>sect. <i>Longipes</i><i> </i>Maguire (<b>Maguire</b>, 1965). By its base of leaf blades gradually   passing into the petiole, apex of leaf blades not abruptly narrowed, the   petiole shorter than the blade, the attenuate portion of the involucral bracts short (&lt; twice as long as the expanded   broader basal portion), and bractlets linear-oblong,   it is most similar to <i>R. spruceana </i>K&ouml;rn. from the R&iacute;o Negro basin in the Amazonian region of   Brazil, Colombia and Venezuela (<b>Berry</b>, 2004). However, <i>R. isanae </i>differs from the latter in its shorter stature   15-30 cm tall (vs. 30-80 cm tall), leaf blades 8-13 cm long, the lower surface   sparse verrucose (vs. 15-30 cm, glandular-punctate),   peduncles 10-15 cm long (vs. 16-35 cm), involucral bracts covered by shorter glandular trichomes in the   basal portion outside, and the attenuate portion 1-5 mm long (vs. glabrous,   10-45 mm long), spikelets shortly pedicellate (vs. sessile), bractlets not ciliate at the margins   (vs. ciliate), petals white, widely-obovate (vs.   yellow, widely-ovate), and the apical appendage of the anthers brown (vs.   purple). </p>     <p>In its   leaf sheath shape, the convex inflorescences, and the petal color, <i>R. isanae </i>also has affinities with <i>R. longipes </i>Spruce ex K&ouml;rn. and <i>R. modesta </i>Maguire, however, it can be distinguished   from these species by the characters indicated in <a href="#t1">Table 1</a>. </p>     <p>    <center><a name="t1"><a href="img/revistas/racefn/v40n157/v40n157a12t1.gif" target="_blank">Table 1</a></a></center></p>     <p><b>Etymology. </b><i>Rapatea</i><i> isanae </i>is named after the Isana river.   This river drains into the Rio Negro; geographically, its basin is nested between the Xi&eacute; (to the   north) and the Vaup&eacute;s (to the south) river basins. Politically, the upper   portion is in Colombia and the lower portion in Brazil (where it is called I&ccedil;ana). The headwaters of the Isana river are considered sacred land for the Kuripaco and Baniwa Indigenous groups, a nation that belongs to   the Arawak language family that number about 14.000 people who has lived for   centuries in the upper R&iacute;o Negro area (<b>Cabrera-Becerra</b>, 2010). This   culture believes that the center of the world (&quot;umbilicus&quot;), where all the   human races began, is found in the pristine region of the upper Isana (<b>Alveiro</b><b> Calero-Cayopare</b>, pers. comm., 2016). This ancient   heritage clearly demonstrates that forests also provide an array of cultural   and spiritual benefits to the people that occupy them. Notwithstanding, these   compensations are only recently being explicitly considered as ecosystem   services (<b>Daniel, <i>et al., </i></b>2012). </p>     ]]></body>
<body><![CDATA[<p><b>Phenology. </b>Known to flower in May, but information   from other times of the year is lacking. </p>     <p><b>IUCN Red List category. </b>According the IUCN   criteria this species would be ranges in DD (data deficient category). In this   grade, more information is required and acknowledges that future research will   show that threatened classification is appropriate (<b>IUCN</b>, 2016).   Currently, <i>R. isanae </i>is known from only two   collections, but we expect this new species to have a wider distribution in the   upper R&iacute;o Negro basin, an area poorly known botanically (<b>Aymard</b><b> &amp; Castro-Lima</b>, 2015).</p>     <p><b>Additional   specimens examined (Paratype): </b></p>     <p><b>Colombia. </b>Guian&iacute;a: Corregimiento de Venado, Comu-nidad Punta   Tigre: same locality and   date as the type. <i>M.     Gonz&aacute;lez, F. Castro-Lima, G. Aymard C., V. Minorta-C., H. Arellano-P., L. Ni&ntilde;o, A. Lozano </i>&amp; <i>C.       Villegas V. 742 </i>(COL); <i>F. Castro-Lima, G. Aymard C., Vladimir Minorta-C., H. Arellano-P., L. Ni&ntilde;o, A.         Lozano, M. Gonz&aacute;lez </i>&amp; <i>C. Villegas V. 18291 </i>(COL). </p>     <p><b>Rapatea</b><b> modesta </b>Maguire,   Bot. Mus. Leafl. 14: 112. 1950. - <i>Rapatea</i><i> longipes </i>Spruce ex K&ouml;rn.   var. <i>modesta</i><i> </i>(Maguire) Maguire, Mem. New York Bot. Gard. 12(3):   100. 1965. <b>Type: </b>COLOMBIA: Comisar&iacute;a del   Amazonas, Trap&eacute;cioAmaz&oacute;nico,   interior regions of trapecio between the Amazon and   Putumayo watersheds, ca. 100 m, Nov 1945, <i>R. E. Schultes 6900 </i>(holotype: NY, isotype:   GH). </p>     <p><b>Taxonomic   history. </b><i>Rapatea</i><i> modesta </i>was described by <b>Maguire </b>based on three specimens   collected in 1945 by Richard Evans Schultes during   his explorations to the &quot;Trapecio Amaz&oacute;nico&quot;,   a broad trapezoid strip of land 150 km long between the Putumayo and Amazon   rivers. Maguire made a detailed description but did not mention an affinity to   his new taxon. Afterwards he wrote to R. E. Schultes and remarked that <i>R. modesta </i>is most closely   related to <i>R. longipes</i>, from which it differs   in its smaller habit, broader, shorter, more conspicuously veined membranous   leaf-sheaths, relatively broader and more numerously veined leaf blades,   considerably larger heads, more acuminate spiked bractlets,   and white rather than yellow petals (<b>Schultes</b>,   1950). In his monograph of the genus <i>Rapatea</i>,   Maguire referred this species to a variety of <i>R. longipes </i>(i.e., <i>R. longipes </i>var. <i>modesta</i><i> </i>(Maguire) Maguire), also providing a   key to separate both varieties (<b>Maguire</b>, 1965). Examination of type   specimen, the study of additional material, and Maguire&#39;s data clearly   indicates that <i>R. modesta </i>should be restablished and treat as distinct species. Because of its bractlets of the spikelets of   equal length and the inflorescence receptacle convex or hemispheric, this species   belongs to <i>Rapatea</i><i> </i>sect. <i>Longipes</i><i> </i>Maguire, and by the base of leaf   blades abruptly constricted above the summit of the sheath forming a long and   slender petiole, <i>R. modesta </i>is most similar to <i>R. longipes</i>, however, these two species can be   distinguished by the characteristics presented in <a href="#t1">Table 1</a>. </p>     <p>The label   of on <i>R. E</i>. <i>Schultes</i><i> 6899* </i>states   (handwritten, but the label data) &quot;red flowers&quot; for <i>R. modesta </i>Maguire. Schultes observed that the red-flowered   form grows together with the white-color form (<b>Schultes</b>,   1950). According to <b>Maguire </b>(1950, 1982), as well as hundreds of   specimens examinated, red flowers have not been   reported for the genus besides this Schultes&#39;s collection (<b>Paul Berry</b>, pers. comm., 2016). We are not questioning Schultes&#39;s field observations, but perhaps he was referring   to the reddish involucral bracts, which can indeed be   reddish, rather than to the petals themselves. </p>     <p><b>Additional   specimens examined: </b></p>     <p><b>Colombia. </b>Amazonas: Trap&eacute;cioAmaz&oacute;nico, interior regions of trapecio between the Amazon and Putumayo watersheds, ca. 100 m, Nov 1946, <i>G. A. Black   &amp; R. E. Schultes 46</i>-<i>361 </i>(NY); ibid,   flowers red, Nov 1945, <i>R. E. Schultes 6899*</i>(COL,   GH, K, NY). P. N. N. R&iacute;o Pur&eacute;, Varillal de Aguanegra, 2&deg; 02&#39; 52.44&#39;&#39;S; 69&deg; 41&#39; 33.96&#39;&#39; O, July 2010, <i>A. Barona 46 </i>(COAH); La Pedrera, La   Tonina, 1&deg; 29&#39; S; 69&deg; 29&#39; O, 10 Oct 1994, <i>D. C&aacute;rdenas, D. Giraldo C. &amp;     E. Yukuna 5750 </i>(COAH).Vaup&eacute;s: <i>R&iacute;</i>o   Apaporis, raudal Jirijirimo, Aug 1951, <i>R. E. Schultes &amp; I. Cabrera 13467 </i>(GH);   R&iacute;o Piraparana, Cerro E-ree-e&eacute;-ko-mee-o-kee.   0&deg; 19&#39; 60&#39;&#39; N; 70&deg; 30&#39; 00&#39;&#39; W, Sep 1952, <i>R. E. Schultes &amp; I. Cabrera 17500 </i>(COL); R&iacute;o Piraparana, Misi&oacute;n San Miguel, Oct 1976, <i>E. W. Davis 127 </i>(COL). </p>     <p><b><i>Rapatea</i></b><b><i> sessiliflora </i></b>(Maguire) Aymard &amp; Arellano-Pe&ntilde;a, <i>comb</i><i>. et stat.   nov.</i>: <i>Rapatea</i><i> paludosa </i>Aubl. var. <i>sessiliflora</i><i> </i>Maguire,   Bull. Torrey Bot. Club 75:   204. 1948. <b>Type: </b>SURINAME: Sipaliwini District: Tafelberg (Table Mountain), Grace Creek, 1 kilometer east of Savanna VIII, 03&deg; 54&#39; N; 56&deg;   20&#39; W, ca. 1000 m, 01 Sep 1944, <i>B. Maguire 24587 </i>(holotype:   NY, isotypes: A, F, U, US). </p>     ]]></body>
<body><![CDATA[<p><i>Rapatea</i><i> sessiliflora </i>was   described as a variety of <i>R. paludosa </i>based on   two specimens (<b>Maguire</b>, 1948). The examination of type specimen and the   additional material indicates that it should be treated as a separate species,   which can be distinguished from <i>R. paludosa </i>by   the following characters: slender plants (vs. stout), leaf blades 40-60 cm   long. 1-2.5(3.5) cm wide (vs. 60-90 cm long, 4-12 cm wide), inflorescences 3-4   cm broad (vs. 4-8 cm broad), apex of the bracts ca. 10 cm long, 2.0-2.5(3.2) cm   wide at the base (vs. 15-20 cm long, 4-6 cm wide), and spikelets sessile or with pedicels 0.5-3 mm long (vs. spikelets with pedicels 5-12(20) mm long). </p>     <p><b>Additional   specimens examined. </b>BRAZIL: Amazonas, <i>In vicinibus Barra </i>(Manaus), December-March 1850-51, <i>R. Spruce s.n. </i>(NY). Amazonas, vicinity of Manaus, Tarum&atilde;, Cachoeira baixa Tarum&atilde;, June 1967, <i>G. T. Prance,     B. S. Pena &amp; J. F. Ramos 3859 </i>(INPA, NY). SURINAME: base of Tafelberg Mountain, Coppename River headwaters, 106 m, July   1944, <i>B. Maguire 24177 </i>(NY); Tafelberg,   Savanna landing strip, March 1961, <i>K. U. Kramer &amp; W. H. A. M. Hekking 3029 </i>(NY, U); Sipaliwini District: Tafelberg National Park, western side of   Lisa Creek, 3&deg; 55&#39; N; 56&deg; 11&#39; W, ca. 1000 m, June 1998, <i>L. G. Lohmann 207 </i>(MO, WIS); Tafelberg Mountain, Grace Creek, 1 km north of Grace fall, 3&deg; 54&#39; 32&#39;&#39; N; 56&deg; 12&#39; 44&#39;&#39; W,   ca. 800-820 m, July 1998, <i>T. Hawkins 1870 </i>(MO, WIS). VENEZUELA: Bol&iacute;var:   r&iacute;os Icabar&uacute; y Hacha, March 1955, <i>L. A. Bernardi s.n </i>(MER, NY). </p>     <p>Key to the   species of <i>Rapatea</i><i> </i>(Modified from   Berry, 2004). Supplementary information 2, <a href="http://www.raccefyn.co/index.php/raccefyn/article/downloadSuppFile/403/1750" target="_blank">http://www.raccefyn.co/index.php/raccefyn/article/downloadSuppFile/403/1750</a>. </p>     <p>1. Leaf   blades 0.5-2.5 cm wide....................................2 </p>     <p>2(1).   Receptacle plane-convex; bractlets strongly   gradate............<i>R. linearis </i>Gleason   (Amazonian of Brazil, Colombia, Guyana) </p>     <p>2. Receptacle shallowly convex, at least hemispheric or   elongate, bractlets equal in   length........................................3</p>     <p>3(2). Leaves blades orange   punctate below, inflorescence elongate, base of the involucral bract deeply cordate........<i>R. xiphoides </i>Sandw. (Guyana: Kaieteur savannas) </p>     <p>3. Leaves   blades if punctate, without orange dots, inflo-rescence shallowly convex or at least hemispheric, base of the involucral bract truncate, rounded or subcordate............4 </p>     <p>4(3). Base   of leaf blades abruptly widened at the base above the petiole; apex of leaf   blade abruptly narrowed; petiole as long as the blade or   longer...................<i>R. longipes </i>Spruce ex K&ouml;rn. (R&iacute;o Negro basin: Amazonian of Brazil, Colombia   and Venezuela) </p>     <p>4. Base of   leaf blades gradually passing into the petiole; apex of leaf blades not   abruptly narrowed; petiole shorter than the   blade.......................................................................5 </p>     ]]></body>
<body><![CDATA[<p>5(4). Apex   of the involucral bracts attenuate 1-45 mm long, &lt;   twice as long as the expanded broader basal portion; lower surface of the leaf   blade glandular-punctate or sparse verrucose mainly   on the lower surface.................................6 </p>     <p>6. Plants   30-80 cm tall; lower surface of the leaf blade glandular-punctate; attenuate   portion of the involucral bracts 10-45 mm long;   peduncle of inflorescence 16-35 cm long, petals yellow.............<i>R. spruceana </i>K&ouml;rn. (R&iacute;o Negro   basin: Amazonian of Brazil, Colombia and Venezuela) </p>     <p>6. Plants   15-30 cm tall, lower surface of the leaf sparsely verrucose;   attenuate portion of the involucral bracts 1-5 mm   long, peduncle of inflorescence 8-13 cm long; petals white..........<i>R. isanae </i>Aymard &amp;   Arellano-Pe&ntilde;a (R&iacute;o Negro basin: Amazonian Colombia) </p>     <p>5.   Attenuate portion of the involucral bracts 20-80 mm   long, 2-4 times longer than the expanded broader basal portion; lower surface   of the leaf blade smooth (not glandular-punctate or sparsely verrucose)............................7 </p>     <p>7(5).   Attenuate portion of the involucral bracts 20-35 mm   long, 2-3.5 times longer than the expanded broader basal portion; lower surface   of the leaf blade densely and minutely papillate;   bracteoles aristate...............<i>R. yapacana </i>Maguire (Venezuela, Amazonas state: savanna Yapacana) </p>     <p>7.   Attenuate portion of the involucral bracts 35-80 mm   long, 4-5 times longer than the expanded basal portion; lower surface of the   leaf blade not minutely papillate; bracteoles acute, apiculate, or sharply acuminate................8 </p>     <p>8(7).   Plants slender; expanded basal portion of involucral bracts   7-12 mm wide; attenuate portion of involucral bracts   35-50 mm long, 4-5 mm broad; leaf blades 3-7 mm wide; peduncle 4-20 cm long,   shorter than the leaves; plants growing in dense circular clumps of numerous   individuals........<i>R. angustifolia </i>Spruce ex K&ouml;rn. (R&iacute;o Negro basin: Amazonian of Brazil, Colombia and   Venezuela) </p>     <p>8. Plants   stout; expanded basal portion of involucral bracts   20-25 mm wide; attenuate portion of involucral bracts   55-85 mm long, 9-14 mm broad; leaf blades 9-15 mm wide; peduncle 35-45 cm long,   longer than, or equal to, the leaves; plants generally growing as solitary   individuals........<i>R. circasiana </i>Garc&iacute;a-Barr. &amp; L. E. Mora (R&iacute;o Negro basin: Amazonian of Brazil,   Colombia and Venezuela) </p>     <p>1. Leaf   blades 3-14 cm wide........................................9 </p>     <p>9(1). Leaf   sheath short, 2-9 (-15) cm long; involucral bracts   1.5-8 cm long, apex narrowed, 0.5-3.5 cm long; heads 1-3 cm   broad...........................................................10 </p>     ]]></body>
<body><![CDATA[<p>10(9).   Base of leaf blades gradually narrowed at the base to a union with the sheath, petiolar portion ca. 0.2 cm long<b>; </b>involucral bracts 6-8 cm long, narrowed apical part 3-3.5   cm long..................<i>Rapatea</i><i> sp. </i>A   (Colombia; Cauca) </p>     <p>10. Base   of leaf blades abruptly widened at the base above the petiole; portion more   than 1 cm long; involucral bracts 1.5-3.5 cm long,   narrowed apical part 0.5-2.5 cm long......11 </p>     <p>11(10).   Leaf sheaths lanceolate, 3 or more times longer than   broad; petiole as long as the blade, leaf blades 3-3.5 cm wide, oblong-linear   to lanceolate; narrowed apical part of the involucral bracts 0.5-1 cm long; peduncle 12-25(30) cm   long; petals yellow...................................<i>R. longipes </i>Spruce ex K&ouml;rn. (R&iacute;o Negro basin: Amazonian   Brazil, Colombia and Venezuela) </p>     <p>11. Leaf   sheaths strongly ventricose, 2-3 times longer than   broad; petiole longer than the blade; leaf blades 3-6 cm wide, oblong-elliptic;   apex 2-3 cm long; narrowed apical part of the involucral bracts 1-2.5 cm long; inflorescence 6-15 cm long; petals white.................................<i>R. modesta </i>Maguire (Amazonian Colombia) </p>     <p>9. Leaf   sheath elongate, 15-30 cm long; involucral bracts   5-25 cm long, apical attenuate portion 3-22 cm long; heads 3-8 cm   broad...........................................................12 </p>     <p>12(9).   Lamina base gradually narrowed to petiole   region..............................................................................13 </p>     <p>13(12). Petiolar region 0.5-3 cm long.........................14 </p>     <p>14(13).   Leaves (4-) 5-9 cm wide; leaves smooth throughout; involucral bracts cordate at the base; bracteoles acuminate,   spotted (maculate) at the apex........<i>R. spectabilis </i>Pilg. (Brazil, Bolivia, Colombia, Ecuador and   Peru) </p>     <p>14. Leaves   3-4 cm wide; lower surface of the leaves slightly scabridulous; involucral bracts truncate at the base; bracteoles cucullate-obtuse, without spots at the apex...... <i>R. scabra </i>Maguire (Venezuela, Amazonas state: Cerro Sipapo) </p>     <p>13. Petiolar region more than 3.5 cm long...................15 </p>     ]]></body>
<body><![CDATA[<p>15(13).   Leaves 4-12 cm wide, inflorescence 4-8 cm broad, involucral bracts 10-20 cm long, cordate, spikelets pedicellate (pedicels 10-20 mm long), widespread in   the Neotropics (from Panama, Trinidad, Venezuela to   Bolivia)................<i>R. paludosa </i>Aubl. </p>     <p>15. Leaves   3-4 cm wide, inflorescence ca. 3 cm broad, involucral bracts 8-10 cm long, involucral bracts rounded or   deeply cordate at the base, spikelet sessile or   pedicels not longer than 3 mm (Brazil, Guayana Shield   of Suriname and Venezuela)..........................................................................16 </p>     <p>16(15). Involucral bracts deeply cordate at the base; spikelet bractlets 5(-7) nerved at the   apex........................<i>R. pycnocephala </i>Seub. (Brazil: Bahia, Goi&aacute;s, Maranh&atilde;o, Mato Grosso, Par&aacute;, Piau&iacute;, Rond&ocirc;nia) </p>     <p>16. Involucral bracts rounded at the base; spikelet bractlets 3-nerved at the apex......................<i>R. sessiliflora </i>(Maguire) Aymard &amp; Arellano-Pe&ntilde;a   (Brazil-Amazonas, Suriname and Venezuela) </p>     <p>12. Base   of leaf blades abruptly constricted above the summit of the   sheath...........................................................17 </p>     <p>17(12).   Floral receptacle elongate...............................18 </p>     <p>18(17).   Leaf blades strongly rugulose; inflorescences 5-14 cm   long......................................................................19 </p>     <p>19(18).   Leaves blades coriaceous, narrower-lanceolate, ca.   3.5 cm long; petiole 8-10 cm long: head 5-8 cm long, bracteoles scarious-membranaceous...................<i>R. rugulosa </i>Maguire (Brazil: Amazonas state) </p>     <p>19. Leaves   blades membranaceous, linear-lanceolate,   6-10 cm wide; sessile, head 6-12 cm long, bracteoles   coriaceous...................<i>R. membranacea </i>Maguire   (Guyana: Pakaraima mountains) </p>     <p>18. Leaf   blades smooth; inflorescences 4-8 cm long.....20 </p>     ]]></body>
<body><![CDATA[<p>20(18).   Leaf blades 1.5-3 cm wide, with 14-16 nerves, orange punctate; receptacle 1.5-2   cm; involucral bracts 15-25 x 1.5-2 cm, cordate, inflorescence ovoid-spherical, 3.5-4 x 3-3.5   cm...................<i>R. xiphoides </i>Sandw. (Guyana: Kaieteur Savannas) </p>     <p>20. Leaf   blades 3-5 cm wide, with 10-12 nerves, if punctate, without orange dots;   receptacle 5-19 cm long; involucral bracts 20-37 x   3-5 cm, rounded or attenuate, inflorescence oblong, 7-8.5 x 5-6 cm.......... <i>R. elongata </i>G. K. Schultze (Brazil and Colombia) </p>     <p>17. Floral   receptacle convex or hemispheric...............21 </p>     <p>21(17).   Leaves blades oblong, abruptly short-acuminate at the apex, constricted at the   base into an evident petiole of 1-20 cm long.................................................................22 </p>     <p>22. Leaves   blades coriaceous, petiolar portion 10-20 cm long;   bracteoles rigid, 3-7-nerved, short-acuminate.........<i>R. muaju </i>Garc&iacute;a-Barr. &amp; L. E. Mora (Brazil-Acre,   Colombia, Ecuador and Peru) </p>     <p>22(21).   Leaves blades membranaceous; petiolar portion 1-10 cm long; bracteoles membranaceous,   3-5-nerved,   long-aristate.......................................................................23 </p>     <p>23(22).   Leaves blades ca. 50 x ca. 10.5 cm; base subcordate to oblique; petiolar portion 8-10 cm long; penducle of the inflorescence 18-25 cm long; bracteoles   5-nerved........................<i>R. saulensis </i>Boom   (French Guiana and Suriname) </p>     <p>23. Leaf   blades 16-21 x 4-8 cm; base inequalateral; petiolar portion 1-3 cm long; penducle of the inflorescence 4-5 cm long; bracteoles 3-5-nerved.................<i>R. undulata </i>Ducke (Amazonian of   Brazil, Colombia and Peru) </p>     <p>21. Leaf   blades lanceolate, gradually acuminate at the apex, cordate or attenuate at the base, with a shorter petiole,   5-20 mm or less of long....................................................24 </p>     <p>24(21).   Leaf blades smooth; inflorescences elongate-hemispheric; bracteoles not all   gradate..............................25 </p>     ]]></body>
<body><![CDATA[<p>25(24).   Leaf blades 33-38 x 5-6 cm, leaf sheaths 10-14 cm long, ventricose......<i>R. ulei </i>Pilg. var. <i>ulei</i><i> </i>(Amazonian of Brazil, Guyana, French   Guiana and Peru) </p>     <p>25. Leaves   blades 40-60 x 10-14 cm, leaf sheaths 20-30 cm long,   elongate....................................................26 </p>     <p>26(25). Inflorescence uni-capitate..............<i>R. ulei </i>Pilg. var. <i>latifolia </i>Maguire (Brazil,   Amazonas state) </p>     <p>26. Inflorescences multicapitate...................<i>R. ulei </i>Pilg. var<i>. latifolia </i>Maguire fm<i>. multicapitata </i>Maguire (Brazil, Amazonas state) </p>     <p>24. Leaves   blades glandular-papillate; inflorescences   shallow-hemispheric to sub-hemispheric; bracteoles evi-dently gradate.....................................................................27 </p>     <p>27(24).   Peduncle 3-14 cm long; involucral bracts broadly deltoid,   nearly as broad as long, 6-10 cm long..................28 </p>     <p>28(27).   Lower surface of leaf sheath densely brown-pubescent with elongate, crisp-villosulous, loose, multi-cellular hairs; upper surface of   leaf with short, divaricate, pointed hairs irregularly scattered on the veins   in addition to the minutely papillate surface; spikelets 16-20 mm long (excluding the sepals); lowest   bracteoles 12-13 mm long; anthers ca. 5 mm long; filaments glabrous.......<i>R. steyermarkii </i>Maguire (Guayana Shield of Guyana and Venezuela) </p>     <p>28. Lower   surface of leaf sheath brown-dotted between smaller, pale punctuations; upper   leaf surface densely verruculose-papillate throughout; spikelets 23-25 mm long (excluding the   sepals); lowest bracteoles 17-18 mm long; anthers ca. 10 mm long; filaments   ciliolate.................<i>R. aracamuniana </i>Steyerm. (Venezuela, Amazonas state: Cerro Aracamuni) </p>     <p>27.   Peduncle 20-50 cm long; involucral bracts lanceolate, longer than broad, 10-25 cm   long...............................29 </p>     <p>29(27).   Bracteoles stiff, obviously different in size, the lower ones much less than   1/2 the length of the spikelet; leaf blades 25-75 cm long, 6-11 cm wide; involucral bracts 10- 20 cm long; lower leaf surface with   the primary veins acutely elevated, separating the broad, flat depressions;   primary veins of upper leaf surface shallowly raised, not presenting a plaited   appearance, 0.5-1 mm apart................<i>R. fanshawei </i>Maguire (including <i>R. fanshawei </i>var. <i>minor</i>) Guayana Shield of Guyana and Venezuela </p>     ]]></body>
<body><![CDATA[<p>29. Bracteoles sub-membranaceous, of nearly equal length; leaf blades ca. 130   cm long, 9-12 cm wide; involucral bracts ca. 25 cm   long; lower leaf surface with shallowly convex surfaces separated by shallow sulcations, lacking acutely elevated primary veins; primary   veins of upper surface conspicuously elevated and presenting a plaited   appearance, 1-2 mm apart............<i>R. chimantensis </i>Steyerm. (Venezuela, Bol&iacute;var state: Chimant&aacute;tepui) </p>     <p><b>Acknowledgments</b> </p>     <p>We gratefully acknowledge the logistic support provided by Compensation   International Progress S.A.-Ciprogress Greenlife- staff: Germ&aacute;n Bernal-G., Alicia Micolta-C., Daniel S. Bernal-L.,   and the Kuripaco indigenous group in the course of a   botanical expedition to the Cuyar&iacute; and Isana rivers sponsored by the &quot;Flor de In&iacute;rida&quot; REDD+ project of the Guayana-Amazonian   transition region. We also thank, Orlando Cordub&iacute; and Lino Flores for their field assistance, the Kuripaco people of the communities of Cejal, Amanadona and Campo Alegre (Cuyar&iacute; river) for their extraordinary effort   carrying hundreds of kilograms of equipment and food along ancestral trails   between the ca&ntilde;oNak&eacute;n and r&iacute;oCuyar&iacute;, and the &quot;raudal&quot; Yurupar&iacute; along the r&iacute;oCuyar&iacute;. To Paul E. Berry   (MICH) for reviewing many times the manuscript, for his constructive feedback,   and for his help improving the key to species of <i>Rapatea</i>.   We also thank Lisa M. Campbell (NY) for reviewing the manuscript, to Gustavo   Romero-G. (AMES) for reviewing the manuscript and for his help in finding   updated literature, and to Carlos Parra-O. (COL) and Dair&oacute;n C&aacute;rdenas-L. (COAH) for their herbarium assistance. Finally, we wish to thank Albeiro Calero Cayopare, a native expert in the Kuripaco language (from Tonina, a village along the Guian&iacute;a river) for his help in translating the abstract into Kuripaco, and for providing information about the   upper Isana River.</p>     <p><b>Conflicts of   interest</b> </p>     <p>The   authors declare that they have no conflict of interest. </p> &nbsp;    <p><font size="3"><b>References</b></font> </p>     <!-- ref --><p><b>Arellano-Pe&ntilde;a, H. y Rangel-Ch, J. O. </b>(2004). Clima del   Choc&oacute; biogeogr&aacute;fico/Costa pac&iacute;fica de Colombia. Pp. 39-82. Colombia Diversidad   Bi&oacute;tica IV. El Choc&oacute; biogeogr&aacute;fico/ Costa Pac&iacute;fica. En: Rangel-Ch. J. O.   (editor), Universidad Nacional de Colombia, Instituto de Ciencias Naturales,   Bogot&aacute;, Colombia.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4619798&pid=S0370-3908201600040001200001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --> </p>     <!-- ref --><p><b>Aymard</b><b>,   G. &amp; Castro-Lima, F. </b>(2015). A   second tree species of <i>Ampelozizyphus</i><i> </i>(Rhamnaceae), from the upper Cuyar&iacute; river basin, Guian&iacute;a (Colombia). <i>Harvard Papers in     Botany </i><b>20: </b>161-166.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=4619800&pid=S0370-3908201600040001200002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --> </p>     ]]></body>
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