Review of the genus perama (Rubiaceae)

The nomenclatural and taxonomic history of the genusPerama Aubl. (Rubiaceae) is discussed. The major trends of evolution within the genus are characterized, and the sections of the genus are delimited. A new section,Diperama Kirkb. & Steyerm., is described. The distribution of the genus is updated, and centers of species concentration are indicated. A complete synonymy is given for the genus, and the type species cited. An artificial key to the species is given ; a new combination,P. parviflora (Standl.) Kirkb. & Steyerm., is mads; and three new species are described,P. harleyi Kirkb. & Steyerm.,P. irwiniana Kirkb. & Steyerm., andP. sparsiflora Standl. ex Steyerm. & Kirkb.     

Jaltomata II: new combinations for five South American species (Solanaceae)

The following species, originally described in the genusSaracha Ruiz & Pav., are transferred toJaltomata, in accordance with contemporary generic boundaries.Jaltomata auriculata (Miers) Mione is distributed from Venezuela to Peru;J. contorta (Ruiz & Pav.) Mione andJ. diversa (J. F. Macbr.) Mione both occur in Peru;J. herrerae (C. V. Morton) Mione is distributed in Peru and Bolivia;J. nitida (Bitter) Mione occurs in Venezuela.     

Taxonomic studies in the Miconieae (Melastomataceae). I. Variation in inflorescence position

In the Miconieae (Melastomataceae) the inflorescences may be either lateral (with shoots pleonanthic and plants showing Rauh's architectural model) or the terminal (with shoots hapaxanthic and plants illustrating Leeuwenberg's, or less commonly Scarrone's or Stone's, architectural models). Inflorescence position is a valuable taxonomic character in the tribe and is usually uniform within genera or speciesgroups. An analysis of variation of this character elucidates the complex and difficult generic delimitations within the tribe.Ossaea DC. andClidemia D. Don, as presently delimited, contain both terminal-and axillary-flowered species and are undoubtedly polyphyletic assemblages. Some groups, e.g.,Clidemia sect.Clidemia, Leandra Raddi sect.Chaetodon Cogn.,Ossaea sect.Octopleura (Griseb.) Cogn., andMyrmidone Mart. have species that develop pseudolateral inflorescences, i.e., the terminal nature of the inflorescence is obscured by the early development of an axillary bud which continues growth of the branch. Pseudolateral inflorescences seem to have evolved several times within the tribe, andClidemia sect.Clidemia likely evolved from the obviously terminal-floweredHeterotrichum DC. andMiconia Ruíz & Pavón sect.Octomeris Hook. f. (p. p.);Myrmidone andMicrophysca Naud. are closely related toTococa Aublet; andLeandra sect.Chaetodon (and probably alsoOssea sect.Octopleura) show affinity with the remaining sections ofLeandra.     

Synopsis of the tribe Bocageeae (Annonaceae), with revisions of Cardiopetalum,Froesiodendron, Trigynaea,Bocagea, and Hornschuchia

The tribal name Bocageeae Endlicher is reestablished and the tribe is circumscribed on the basis of solitary internodal ebracteate pedicels that are articulated at the base, and pollen shed in polyads of eight or more grains. Septate anther locules, large pollen size, and seed appendages are prevalent in the tribe. Intectate pollen with free-standing columellae, rare in Annonaceae, occurs not only in the genusTrigynaea but also in some species ofBocagea andHornschuchia. As defined here, the Bocageeae include seven neotropical genera:Cymbopetalum, Porcelia, Bocagea, Cardiopetalum, Froesiodendron, Hornschuchia, andTrigynaea. The latter five genera are revised and the treatments include ten new species:Cardiopetalum plicatum, Froesiodendron urceocalyx, Hornschuchia lianarum, H. santosii, H. leptandra, Trigynaea cinnamomea, T. lanceipetala, T. triplinervis, T. lagaropoda, andT. axilliflora, all from tropical South America. A new combination,Froesiodendron longicuspe, changes the rank of that taxon from subspecies to species.Cardiopetalum surinamense is removed fromFroesiodendron and reassigned toCardiopetalum on the basis of its connate petals, dehiscent monocarps, and seeds with bilobed arils. A cladogram provides an explicit hypothesis of intergeneric relationships in the tribe. The new combinationOnychopetalum periquino, based onTrigynaea periquino, is made.     

A reevaluation of the tribes Hippotideae and Tammsieae (Rubiaceae)

Rova, J. H. E. & Andersson, L. 1995. A reevaluation of the tribes Hippotideae and Tammsieae (Ruhiaceae). — Nord. J. Bot. 15: 269–284. Copenhagen. ISSN 0107–055X. The genera Hippotis, Pentagonia, Sommera, and Tammsia, the hippotides, have recently been removed from their traditional position in the tribe Isertieae and proposed to form two separate tribes, Hippotideae (the three former genera) and Tammsieae (the latter one). In the most recent overview of the classification of the Ruhiaceae, the position of these tribes was considered uncertain. The morphology and micromorpho-logy of representatives of all genera were reexamined and data were analysed cladisti-cally. It is concluded that the original distinction between the Hippotideae and Tammsieae was based on faulty observations, the hippotides being uniform in ovary morphology. The cladistic analysis suggests that the hippotides form a monophyletic group, within which Tammsia is nested. It is therefore proposed that Tammsieae should he reduced to a synonym of Hippotideae. There are no indications that the hippotides should he reunited with the Isertieae. The genus Wiasemsba Klotzsch is shown to he synonymous with Tammsia, and it is argued that the genus Striolaria Ducke is synonymous with Pentagonia.     

The classification of the generic segregates of Phrygilanthus (= Notanthera) of the Loranthaceae

The taxonomic composition ofPhrygilanthus has long been a source of confusion. Until recently the genus was considered to be distributed from Mexico, Central and South America, to Australia, New Guinea, and the Philippines. Analyses of floral morphology, inflorescence structure, life form, fruit type, and especially chromosome numbers indicate thatPhrygilanthus, as classically circumscribed, is a highly heterogeneous and artificial assemblage containing elements now referable to the following ten genera:Cecarria, Desmaria, Gaiadendron, Ligaria, Muellerina, Notanthera, Psittacanthus, Struthanthus, Tripodanthus, andTristerix. Phrygilanthus itself is nomenclaturally illegitimate and must be replaced by Notanthera. A synopsis of the genera segregated from thePhrygilanthus group is included. A key to the New World genera of Loranthaceae is also appended as well as a nomenclator indicating the present generic status of taxa at one time or another assigned toPhrygilanthus. One genus,Cecarria, is described as new; five new combinations are made:Cecarria obtusifolia (Merr.) Barlow,Psittacanthus palmeri (Wats.) Barlow & Wiens,Struthanthus panamensis (Rizzini) Barlow & Wiens,Tristerix aphyllus (DC.) Barlow & Wiens, andTristerix grandiflorus (Ruiz & Pavon) Barlow & Wiens.     

Miscellaneous mistletoe notes, 1–9

Three new species,Cladocolea biflora Kuijt,Struthanthus condensatus Kuijt, andS. lojae Kuijt are described and six new combinations,Cladocolea diversifolia (Benth.) Kuijt,C. lenticellata (Diels) Kuijt,Dendrophthora virgata (Trel.) Kuijt,Korthalsella chilensis (Hook. & Arn.) Kuijt,Phthirusa retroflexa (Ruiz & Pavon) Kuijt, andStruthanthus flexilis (Rusby) Kuijt are proposed. Nomenclature of two more neotropical Loranthaceae,Psittacanthus ramiflorus (DC.) G. Don andStruthanthus interruptus (H.B.K.) Blume is revised.     

Tropaeolaceae: 685. TROPAEOLUM CILIATUM

Tropaeolum ciliatum Ruiz. & Pav. is described and illustrated. Its habitat in the wild, and its pollination, are discussed and instructions for its successful cultivation are given.     

Molecular Phylogenetic Analysis of Petunia Juss. (Solanaceae)

Representatives from 11 Petunia Jussieu species in south and southeast Brazil were compared with two Calibrachoa La Llave & Lex., one Bouchetia Dunal, and two Nierembergia Ruiz & Pav. taxa in relation to DNA molecular variability. A total of 4532 base pairs related to one nuclear, five plastidial and one mitochondrial systems was investigated. Petunia and Calibrachoa, although separated among themselves, clearly differentiate from the two other genera. Despite the fact that the Petunia species do not show marked molecular differences, they can be separated in two complexes, in good agreement with altitude data. Petunia + Calibrachoa should have diverged from other clades at about 25 million years before present.     

Generic delimitations of Central American Bignoniaceae

Generic delimitations in the Bignoniaceae are discussed, a number of Central American genera are reduced to synonymy, and a new genusPseudocatalpa is proposed. Generic mergers includeLevya withCydista, Saldanhaea withCuspidaria, Doxantha withMacfadyena, Pseudocalymma withPachyptera, andPhaedranthus withDistictis. New combinations necessitated by these mergers include the following:Arrabidaea costaricensis (Kränzl.) Gentry,A. pubescens (L.) Gentry,Cuspidaria floribunda (DC.) Gentry,C. weberbaueri (Spr.) Gentry,Cydista aequinoctialis var.hirtella (Benth.) Gentry,Distictis buccinatoria (DC.) Gentry,Macfadyena unguiscati (L.) Gentry,Melloa quadrivalvis (Jacq.) Gentry,Pachyptera alliacea (Lam.) Gentry,P. hymenaea (DC.) Gentry,P. kerere var.incarnata (Aubl.) Gentry,P. standleyi (Steyerm.) Gentry, andPseudocatalpa caudiculata (Standl.) Gentry. In addition, the fruits of several species are described for the first time, and their taxonomic significance is discussed.     

Revision of the tribe Colpopterini Gnezdilov, 2003 (Homoptera, Fulgoroidea: Nogodinidae)

The tribe Colpopterini Gnezdilov, 2003 is revised, upgraded to the subfamily Colpopterinae, stat. n., and transferred from the family Issidae Spinola to Nogodinidae Melichar. The tribe Colpopterini is recorded from the Afrotropical Region for the first time—Bumerangum deckerti gen. et sp. n. is described from Southern Africa. The tribe Colpopterini s. str. comprises 6 genera: Bumerangum gen. n., Caudibeccus Gnezdilov et O’Brien, 2008, Colpoptera Burmeister, 1835, Jamaha Gnezdilov et O’Brien, 2008, Neocolpoptera Dozier, 1931, and Ugoa Fennah, 1945. The genera Cheiloceps Uhler, 1895, Tempsa Stål, 1866, Eupilis Walker, 1857, and Gabaloeca Walker, 1870 are transferred to the tribe Issini Spinola of the family Issidae. Issus longulus Lethierry, 1890 is transferred to the genus Colpoptera Burmeister. A key to the genera and a list of the species of the tribe Colpopterini are given. Morphological data confirming independent evolution of similar ovipositor types in the families Issidae and Nogodinidae are provided. The term “styletization” is suggested for describing the transformation of the ovipositor from a rounded to an elongate type.     

Balliella,a new genus of ceramiaceae (Rhodophyta)

Detailed studies of various aspects of the morphology and reproduction ofAntithamnion subcorticatum Itono andAntithamnion crouanioides Itono show that these species are incorrectly referred to as the genusAntithamnion. To include these species, a new genus,Balliella, is proposed. In addition, some other algae possibly referable to this genus are briefly discussed. The genusBalliella is here recognized as a member of the new tribeDelesseriopsieae which is most nearly related to the tribe Antithamnieae in the Ceramiaceae. The tribe Delesseriopsieae is now recognized to include the two genera, i.e.,Delesseriopsis andBalliella.     

Cleaning up the grasses dustbin: systematics of the Arundinoideae subfamily (Poaceae)

Among the 12 subfamilies currently considered in the systematics of Poaceae, the Arundinoideae have long been considered as a dustbin group, with a diversity of forms putatively hiding incertae sedis. Because this subfamily has been poorly investigated using molecular markers for the last two decades, the present study provides the first complete phylogeny of the Arundinoideae based on five plastid DNA loci sequenced for 12 genera, and analysed with and without plastome data from previous studies. The refined Arundinoideae appear to be a robust evolutionary lineage of Poaceae, divided into three tribes with some biogeographical patterns: (1) tribe Arundineae, the most heterogeneous tribe, including Eurasian Arundo, Australian Amphipogon and Monachather, and South African Dregeochloa; (2) tribe Crinipedeae (described here), including Crinipes, Elytrophorus, Styppeiochloa and Pratochloa (described here), with a South and East African distribution; and (3) tribe Molinieae, including Hakonechloa, Molinia and Phragmites, with a Eurasian distribution. Despite reduction in size, this small subfamily conserves a high diversity of morphological forms, with several small but highly differentiated genera. Finally, the molecular dating approach provides an evolutionary framework to understand the diversification of Arundinoideae, refuting Gondwanan vicariance between genera and suggesting capability for long distance dispersal.     

Comparative floral morphology in Lycieae (Solanceae)

Comparative organography (excepting carpels studied previously) and anatomy of the flower are reported for some American members of the genera of Lyciaeae:Lycium, Grabowskia, andPhrodus. Data obtained are mostly new since no comprehensive floral anatomical work has been carried out in the tribe. These results include the first report of extrafloral nectaries on the inner epidermis of the calyx inPhrodus andGrabowskia. Results are discussed and compared with previous reports for the family, older than the exclusively AmericanPhrodus andGrabowskia. Lycium shows great morphological diversity while the other two genera are less variable but have more specialized features. A key, based on floral characters, to the genera, of Lycieae and sections ofLycium is provided.     

Anatomy of the floral nectaries of some neotropical Salacioideae (Celastraceae)

Floral nectaries have contributed to the systematics of different taxonomic groups. Since those of the neotropical genera included in subfamily Salacioideae—Cheiloclinium Miers, Peritassa Miers, Salacia L. and Tontelea Aubl.—have different forms and positions, we explored their anatomy to delimit more precisely the genera of subfamily Salacioideae. Buds and open flowers of six species were treated following the usual techniques in plant anatomy. The obtained data were helpful in characterizing the floral nectary anatomy of the studied species. Furthermore, some features such as form, position and surface of nectaries; form of their epidermal cells; presence and distribution of stomata; occurrence of idioblasts containing druses in the nectariferous parenchyma; and absence of nectary vascularization can contribute to the taxonomy and phylogeny of the Salacioideae studied. In most of the studied species the nectar is probably released by both the stomata and the nectary epidermal surface. In Cheiloclinium cognatum, the structure acknowledged as nectary is actually a vestigial tissue and the functions of attracting and rewarding pollinators has phylogenetically migrated to the stigmatic region. The druses and phenolic substances observed in the nectariferous parenchyma probably help defend flowers against herbivore attacks. The minute size of the nectaries of Salacioideae may explain the absence of vascularization. The floral nectaries of Salacia elliptica are epithelial while those of the other species are mesenchymal.     

Karyological features and cytotaxonomy of the tribe Vernonieae (Asteraceae)

Chromosome numbers are reported for 29 populations of 19 Vernonieae taxa collected mainly in the northeastern region of Brazil. Among them, data for five genera (Blanchetia, Rolandra, Pithecoseris, Stilpnopappus and Vanillosmopsis) are here reported for the first time, and the first chromosome counts are presented for 12 species. Chromosome numbers are quite diverse among and sometimes within genera, especially in the controversial and large subtribe Vernoniinae. The numbers varied from 2n = 18 to 2n = ~72. The main karyoevolutionary mechanism seems to be dysploidy, while polyploidy is probably associated with ancient hybridization processes generating most paleotetraploid genera. All studied species presented semi-reticulated interphase nuclei and proximal-early condensing behavior in prophase to prometaphase. In one species (Vernonia condensata with 2n = 40) fluorochrome staining with CMA/DAPI revealed five chromosome pairs bearing subterminal CMA⁺/DAPI^? heterochromatin, probably NOR-associated, revealing the existence of low amounts of satellite DNA. The role of these features in the evolution of the tribe is discussed, revealing some interesting aspects for understanding of the Vernonieae karyoevolution, especially regarding neotropical members.