María Amalia Scataglini

Phylogeny of the Paniceae (Poaceae: Panicoideae): integrating plastid DNA sequences and morphology into a new classification

Included in the PACMAD clade of the family Poaceae (Panicoideae, Arundinoideae, Chloridoideae, Micrairoideae, Aristidoideae, Danthonioideae), the tribe Paniceae s.l. is one of the largest tribes of the subfamily Panicoideae, with more than 2000 species. This tribe comprises a huge morphological, cytological and physiological diversity represented by different inflorescence types, several basic chromosome numbers, and at least four major photosynthetic pathways. The tribe Paniceae has been the subject of molecular studies that have confirmed its paraphyly: two major clades were recognized based on their basic chromosome numbers (x = 9, x = 10). The x = 10 Paniceae clade is sister to the Andropogoneae–Arundinelleae s.s. clade (x = 10), while the combined x = 10 clade is sister to the x = 9 clade that contains the remaining genera of Paniceae. As a result of a recent realignment within the tribe in terms of the phylogenetic position of minor and major Paniceae genera, a reanalysis of the whole sampling is performed and new underrepresented taxa are discussed. A total of 155 genera, currently considered within subfamily Panicoideae, are represented here by almost all genera of Paniceae s.l., representatives of Andropogoneae and Arundinelleae s.s., and the endemic and small tribe Steyermarkochloeae; we also included specimens of subfamily Micrairoideae, tribes Isachneae and Eriachneae. The sampling includes as outgroups 18 genera of the PACMAD clade (excluding Panicoideae) and four genera from the BEP clade (Bambusoideae, Ehrhartoideae, Pooideae), rooting with Bromus inermis. A matrix with 265 taxa based on the combined evidence from ndhF plastid sequences (2074 bp) and 57 morphological characters was subjected to parsimony analyses. Jackknife resampling was used to calculate group support. Most clades are characterized by morphological, cytological, anatomical, and/or physiological characters. Major tribal changes are based on the basic chromosome number; the pantropical x = 9 clade is here recognized as Paniceae s.s., while the American x = 10 Paniceae s.l. is restricted to the reinstated tribe Paspaleae. The optimization of the photosynthetic pathway for the Paspaleae–Andropogoneae–Arundinelleae s.s. clade, including the monotypic Reynaudia, shows a plesiomorphic C4 state while the ancestral state for Paniceae s.s. is ambiguous. If Reynaudia were not included or placed elsewhere, the ancestral photosynthetic pathway for both the Paspaleae–Andropogoneae–Arundinelleae s.s. clade and the Paniceae s.s. would be unambiguously C3. In order to explore character evolution further, the morphological characters were mapped onto one of the most parsimonious trees. A relationship between photosynthetic pathways and inflorescence morphology is suggested here for the first time. Based on the optimization of morphological characters and additional data, we propose names for almost all inner clades at the rank of subtribe with a few groups as incertae sedis. With this extensive sampling, we resolved the phylogenetic relationships and the assignation of synapomorphies, and improved the support in subtribe sorting; consequently a robust circumscription of the tribe Paniceae s.l. is proposed.

Diversity of Boll Weevil Populations in South America: A Phylogeographic Approach

A phylogeographic approach was conducted to assess the geographic structure and genetic variation in populations of the boll weevil Anthonomus grandis, which is the most harmful insect pest of cotton in the Americas. COI and COII mitochondrial gene sequences were analyzed to test a former hypothesis on the origin of the boll weevil in Argentina, Brazil and Paraguay, using samples from Mexico and USA as putative source populations. The analysis of variability suggests that populations from South American cotton fields and nearby disturbed areas form a phylogroup with a central haplotype herein called A, which is the most common and widespread in USA and South America. The population from Texas has the A haplotype as the most frequent and gathers in the same group as the South American populations associated with cotton. The sample from Tecomán (México) shows high values of within-nucleotide divergence, shares no haplotype in common with the South American samples, and forms a phylogroup separated by several mutational steps. The sample from Iguazú National Park (Misiones Province, Argentina) has similar characteristics, with highly divergent haplotypes forming a phylogroup closer to the samples from cotton fields, than to the Mexican group. We propose that in South America there are: populations with characteristics of recent invaders, which would be remnants of “bottlenecks” that occurred after single or multiple colonization events, probably from the United States, and ancient populations associated with native forests, partially isolated by events of historical fragmentation.

Phylogeny of the Pantomorus–Naupactus complex based on morphological and molecular data (Coleoptera: Curculionidae)

The Pantomorus–Naupactus complex is a Neotropical group of broad‐nosed weevils (Coleoptera: Curculionidae) including several parthenogenetic species usually assigned to the genera Naupactus Dejean, Pantomorus Schoenherr, Asynonychus Crotch, Aramigus Horn, Eurymetopus Schoenherr and Graphognathus Buchanan. Sixteen species were studied to test hypotheses on the monophyly of these genera, and on the origin of the parthenogenetic lineages. A matrix of 30 morphological characters and 999 positions of the Cytochrome Oxidase I gene, was analyzed with separate partitions and simultaneously, under equal and implied weights, and with different transversion/transitions costs. The ILD test indicates that the incongruence between the molecular and morphological data is not significant. Under equal weights, the molecular data resulted in a single tree and morphology in 34 trees; under implied weights morphology gave a different tree, and under TV:TS ≥ 4:1 molecular and combined analyses resulted in the same optimal tree. According to the latter, Naupactus includes Graphognathus, and is thus paraphyletic and basal regarding remaining genera, Pantomorus is polyphyletic and includes Aramigus and Asynonychus, and Eurymetopus is monophyletic. The species in which apomictic parthenogenesis has been verified (Aramigus tessellatus, Asynonychus cervinus and Graphognathus lecuoloma), belong to different clades of the Pantomorus‐Naupactus complex, with basal sexual relatives.

Dispersal of the cotton boll weevil (Coleoptera: Curculionidae) in South America: evidence of RAPD analysis.

RAPD technique provides useful information on the geographic origin and dispersal of the boll weevil Anthonomus grandis in South America. Nine populations from Argentina, Brazil, Paraguay, Mexico and USA were analyzed. Weevils were captured on native plants (Misiones province, Argentina) and on cotton cultures, except the sample from the United States (USDA laboratory-reared colony). A sample of the ‘Peruvian square weevil’, A. vestitus, from Ecuador, was included in the analysis in order to compare interspecific variation. The four primers used in the analysis revealed 41 ‘anonymous loci’. The neighbor-joining tree based on Neis distances and values of Nm (migrants per generation), indicate that genetic similarity between samples from Tecomán (Mexico) and Puerto Iguazú (Argentina), is higher than among remaining South American populations. This result supports an hypothesis of natural occurrence of the boll weevil in South America, prior to extensive cotton cultivation. Population outbreaks of the species would be associated with increase of agricultural lands.

Phylogeny of New World Paspalum (Poaceae, Panicoideae, Paspaleae) based on plastid and nuclear markers

Phylogenetic analyses of 131 terminals of Paspalum and related genera, based on both plastid and nuclear markers, were performed under maximum parsimony and Bayesian methods. The total evidence analyses generated a hypothesis showing that Paspalum would be monophyletic if Spheneria, Thrasyopsis and Reimarochloa are included within the genus. Paspalum inaequivalve and P. microstachyum, two species of the Inaequivalvia group were related to genus Anthaenantiopsis, excluded from Paspalum, or nested within it by plastid and nuclear markers, respectively. Subgenera Anachyris and Harpostachys were partially recovered as monophyletic assemblages, while subg. Ceresia and Paspalum resolved as polyphyletic. Within subgenus Paspalum, some informal groups were recovered as monophyletic, while others were resolved as paraphyletic or polyphyletic. Phylogenetic relationships among species of Paspalum were partially recovered possibly due to reticulation events among species, autopolyploidization and apomixis; all these processes being common in Paspalum, thus obscuring the infrageneric classification.

Phylogeny of sections Clavelligerae and Pectinatae of Panicum (Poaceae, Panicoideae, Paniceae): establishment of the new subtribe Dichantheliinae and the genus Adenochloa

Taxonomic features of African species of Panicum sections Clavelligerae and Pectinatae are reviewed and compared with Dichanthelium and other taxa in tribe Paniceae. The new subtribe Dichantheliinae is proposed on the basis of molecular and morphological characters: it includes non-Kranz species, growing at forests edges or in mountain grasslands with membranous-ciliate ligules, lax and open inflorescences, ellipsoid to oblongoid spikelets, and an indurate upper anthecium. Within the Dichantheliinae, the new genus Adenochloa is also established on the basis of chloroplast ndhF sequences and morphological characters, i.e., plants with clavellate multicellular, and glandular hairs present on blades, main axis, branches, and pedicels of inflorescences; ellipsoid to oblongoid, glabrous spikelets, with a lower glume 1/3 to more than 1/2 the length of the spikelet; a 7–13-nerved upper glume and a 5–9-nerved lower lemma; the upper anthecium is indurate, pilose or glabrous. Adenochloa includes 14 species from Africa and Madagascar. The new combinations: Adenochloa adenophylla, A. adenophora, A. bullockii, A. claytonii, A. ecklonii, A. flacciflora, A. habrothrix, A. hymeniochila, A. lukwangulense, A. nigromarginata, A. pectinella, A. pole-evansii, A. sadinii, and A. squarrosa are proposed and the new genus is compared with other genera of the tribe Paniceae. Also, lectotypes are designated for Brachiaria sadinii, Panicum adenophorum, P. adenophyllum, P. ecklonii, P. katentaniense, P. kisantuense, P. hymeniochilum, P. hymeniochilum var. glandulosum, P. snowdenii, and P. scandens; Panicum glanduliferum and P. omega are treated as new synonyms of Adenochloa hymeniochila and A. pectinella, respectively. Finally, new illustrations are provided for 6 species of the new genus.

Phylogenetic analysis and taxonomic position of section Verrucosa of Panicum and its relationship with taxa of the Sacciolepis–Trichanthecium clade (Poaceae: Panicoideae: Paniceae)

The new genus Kellochloa is proposed, on the basis of morphological and molecular characters, to include two North American species of Panicum s.l., previously classified in sect. Verrucosa: P.brachyanthum and P. verrucosum. Both species are annual, with decumbent culms branching divaricately at the lower nodes, and erect culms with terminal and axillary inflorescences. The spikelets are pilose, with lower glume 1/6 to 1/4 the length of the spikelet, upper glume and lower lemma subequal, 3–5-nerved, the lower anthecium reduced to the lower lemma, and upper anthecium indurate, with bicellular microhairs and simple papillae evenly distributed all over the lemma and palea. Molecular phylogenetic studies, analyzing plastid ndhF and rpoA sequences, confirmed that these morphological characters are differential. The phylogenetic position and taxonomic features of the new genus are established and compared with Panicum s.str. and other taxa of the Sacciolepis–Trichanthecium clade. Full synonymies and descriptions, a distribution map, illustrations of both species, and a key are provided. Two new combinations are proposed. In addition, four African ungrouped species of Panicum s.l. were, for the first time, included in the phylogenetic analysis to analyze their relationship with the new genus and its positions in the Sacciolepis–Trichanthecium clade.

Phylogeny of Digitaria Sections Trichachne and Trichophorae (Poaceae, Panicoideae, Paniceae): A Morphological and Molecular Analysis. New Circumscription and Synopsis

Abstract The present study provides evidence for taxonomic delimitation of Digitaria sect. Trichachne based on morphological data (micro- and macromorphology) and molecular data. A phylogenetic analysis was performed using 121 morphological characters and ITS sequences of 22 species and one variety of Digitaria plus three outgroups. In all topologies (based on morphological, molecular, and combined data) Digitaria sect. Trichophorae was non-monophyletic and nested within D. sect. Trichachne. Digitaria sect. Trichophorae is thus synonymized under D. sect. Trichachne and the circumscription of D. sect. Trichachne is emended. Diagnostic morphological characters related to spikelet structure are described and documented with SEM. A key to taxa belonging to D. sect. Trichachne is provided, as well as a synopsis including synonymy, iconography, geographical distribution, and ecology. The neotype of Trichachne sacchariflora Nees is herein designated. Complete illustrations of Digitaria eggersii, D. hitchcockii, and D. patens are provided. The phylogenetic placement of the Australian species D. brownii differed among trees resulting from different data sets, thus it is provisionally not included in D. sect. Trichachne in spite of its morphological similarity. Furthermore, Megaloprotachne albescens is formally transferred to Digitaria, as Digitaria albescens.

A New Species of Mastigostyla (Iridaceae) from Argentina

Abstract We describe and illustrate Mastigostyla coronata, a new species of Iridaceae from the high Andes of Jujuy (Argentina), morphologically similar to Mastigostyla vargasii. The inclusion of this new species in Mastigostyla is supported by a phylogenetic analysis based on plastid markers. We also present a morphological comparison among the sub-acaulescent species of Mastigostyla (including Cardenanthus), and a key to those species.