Three new species of <Emphasis Type="Italic">Passiflora</Emphasis> subgenus <Emphasis Type="Italic">Decaloba</Emphasis> (Passifloraceae) from Brazil

Three new species from Brazil are described and illustrated. Passiflora cervii, P. jiboiaensis, and P. transversalis all belong to Passiflora subg. Decaloba.     

Four new species of the Didymopanax group of <Emphasis Type="Italic">Schefflera</Emphasis> (Araliaceae) from the Brazilian Amazon

Four new species of the Didymopanax group of Neotropical Schefflera (Araliaceae) from the Brazilian Amazon are here described and illustrated. Two of these are mainly known from the surroundings of Manaus, Amazonas state (Schefflera ciliatifolia and Schefflera umbrosa). The first is distinguished by its ciliate leaflets, while the second is characterized by leaflets varying in shape from trilobed to entire. Schefflera plurifolia is known only from southern Amazonian forests, and is remarkable in its pinnately-compound leaflets. Schefflera dichotoma, only known from the type collected on “campinarana” forests from Upper Rio Negro, at the municipality of São Gabriel da Cachoeira (Amazonas), is characterized by dichotomously branching inflorescences. Comments on the geographic distribution and ecology of the new species are provided, as well as an identification key to the species of the Didymopanax group found in Brazilian Amazonian rainforests and savannas.     

Three new species of <Emphasis Type="Italic">Davilla</Emphasis> (Dilleniaceae) from Bahia,Brazil

Three new species of Davilla (Davilla sessilifolia, Davilla minutifolia and Davilla aymardii) from Bahia, Brazil, are described and illustrated. Affinities and diagnostic characteristics of each species are discussed. The new species belong to Davilla sect. Homalochlaena.     

Two new species of <Emphasis Type="Italic">Goniopteris</Emphasis> (Thelypteridaceae) from Brazil

Two new species of Goniopteris endemic to the state of Espírito Santo (Brazil) are described and illustrated: Goniopteris bradei and G. salinoi. Morphological comparisons with similar species, as well as two identification keys, are presented. One key includes the Brazilian species most similar to G. bradei, and the other includes those Goniopteris species with glandular hairs, including G. salinoi.     

<Emphasis Type="Italic">Magnolia brasiliensis</Emphasis> (Magnoliaceae), a new species and new record for the Northeastern region of Brazil

A new species of Magnolia is described for the flora of Brazil, based on material from Bahia and Minas Gerais states. This species represents the first record of Magnoliaceae in the Northeastern region of Brazil. Magnolia brasiliensis differs from all other Brazilian species of Magnolia by having adaxially glossy leaves and differs from M. ovata by having a lower number of stamens and carpels. Despite its large extent of occurrence, the conservation status attributed to the new species is Endangered, mainly based on the low number of mature individuals in each subpopulation (< 50) and an area of occupancy of less than 16 km².     

Two new species of <Emphasis Type="Italic">Miconia</Emphasis> (Melastomataceae,Miconieae) from the Brazilian northern border and adjacent French Guiana

Two new species of Miconia from northern Amazonia area described. Miconia amapaënsis has been collected in the Brazilian state of Amapá and in nearby locations in northern Pará and southern French Guiana. It has remarkable seeds, with both the appendix and seed coat covered with long papillae. Miconia forzzae has been collected on the Brazilian side of the Neblina Massif, in the Brazilian state of Amazonas, close to the border with Venezuela. It has 4-merous flowers, with a terete hypanthium, yellow stamens, the ovary apex with unbranched trichomes, and a punctiform stigma. This species may be endangered, considering its narrow distribution, and the fact that it was collected between 2000 and 2100 m elevation in an isolated mountain range with no neighboring mountains with similar height, but we assess its conservation status as “data deficient”, due to a lack of knowledge on the situation of the populations and the number of individuals.     

Two New Species and New Occurrences of <Emphasis Type="Italic">Syneches</Emphasis> Walker for Brazilian Biome of Caatinga (Diptera: Hybotidae: Hybotinae)

Syneches from Brazilian biome of Caatinga were studied, two new species are described, Syneches atratus sp. nov. and Syneches limeirai sp. nov., and three species, Syneches annulipes Bezzi, 1909, Syneches moraballi Smith, 1963, and Syneches rafaeli Ale-Rocha & Vieira, 2008, are recorded for the biome. An identification key for the species of Syneches from Caatinga biome is provided.     

Revision of the <Emphasis Type="Italic">Serrulati</Emphasis> species of <Emphasis Type="Italic">Penstemon</Emphasis> section <Emphasis Type="Italic">Saccanthera</Emphasis> subsection <Emphasis Type="Italic">Serrulati</Emphasis>

A revision of Penstemon sect. Saccanthera subsect. Serrulati includes a new species (P. salmonensis), a new variety (P. triphyllus var. infernalis), and the elevation of a subspecies to species (P. curtiflorus), bringing the total number of species to eight, which are keyed and described, complete with nomenclature and type citations.     

Bioactive phytochemicals from shoots and roots of <Emphasis Type="Italic">Salvia</Emphasis> species

The plants of the genus Salvia L. are important medicinal herbs of the Lamiaceae family and some of them such as S. officinalis (sage), S. miltiorrhiza (red sage, Danshen) and S. sclarea (clary sage) have been used as medicinal plants in the folk medicine of several countries. In this review, we discuss the reports that have examined Salvia species with the aim of isolation of pure compounds with different biological activities. The phytochemical analyses of various sage plants have reported 10 monoterpenoids (1–10), 1 sesquiterpenoid (11), 8 labdane (13–20), 15 ent-kaurane (21–35), 82 abietane, rearranged abietane and tanshinone (36–117), 3 icetexane (118–120), 43 clerodane (121–163), and 3 pimarane (164–166) diterpenoids with cytotoxic and antimicrobial, antiprotozoal, antioxidant, phytotoxic and insecticide effects. The other heavier terpenoids, including 3 sesterterpenes (167–169), 10 triterpenoids and β-sitosterol (170–180) have been introduced as minor bioactive compounds in the sage plants. Sahandinone (107), 6,7-dehydroroyleanone, 7-α-acetoxyroyleanone (40), and tanshinone like diterpenoids have been isolated from the roots’ extracts of different Salvia species. On the other hand, several radical scavenger phenolic compounds like simple phenolics and caffeic acid derivatives (181–201) including rosmarinic acid, flavonoids (202–217) as well as phenolic diterpenoids, such as carnosol and carnosic acid have been isolated from the aerial parts of these plants. One pyrrole (218) and 3 antimicrobial oxylipins (219–221) are among the other less detected constituents in the members of Salvias. Furthermore, sages also synthesize antifungal, antileishmanial and antimalarial phytochemicals in their roots and shoots, which are reviewed in this paper. We also examine the allelopathic phenomena and the ecologically important phytochemicals identified in different parts of the sage plants. Finally, antifeedant and insecticide phenomena, which are due to the presence of volatile monoterpenes and clerodane diterpenes in these plants, are discussed. Considering the presence of diverse biologically active phytochemicals in the sage plants, they can be suggested as suitable candidates for the formulation of valuable natural medicines.     

A new species of <Emphasis Type="Italic">Panopsis</Emphasis> (Proteaceae) from Bahia,Brazil

Recent collections from Bahia, Brazil included a new species of Panopsis from the Atlantic rainforest. So far it is only known with fruits, which are much larger than in most species of the genus. Panopsis magnifructa is described and compared to other species in the genus. It is only the second species of the genus known in the State of Bahia, Brazil.     

<Emphasis Type="Italic">Myrcia incompleta</Emphasis> (Myrtaceae), a new species from Amazonian Brazil

Myrcia incompleta, from the northern Brazilian states of Amazonas and Rondônia, is described and illustrated. This species is apparently related to Calyptranthes paniculata and C. speciosa, from which it is distinguished mainly by its narrower leaves with midvein strongly raised adaxially and shorter, pauciflorous inflorescences. Conservation status for the species is proposed.     

Differential alkaloid profile in <Emphasis Type="Italic">Uncaria tomentosa</Emphasis> micropropagated plantlets and root cultures

The alkaloids of Uncaria tomentosa micropropagated plantlets and root cultures were isolated and identified by NMR and mass spectrometry. Plantlets yielded pteropodine (1), isopteropodine (2), mitraphylline (3), isomitraphylline (4), uncarine F (5), speciophylline (6), rhynchophylline (7) and isorhynchophylline (8). In plantlets growing under continuous light, tetracyclic alkaloids 7 and 8 decreased from 20 ± 1.8 at 2 months to 2.2 ± 0.33 mg/g dry wt at 6 months, while the pentacyclic alkaloids 1–4 increased from 7.7 ± 1.4 to 15 ± 0.05 mg/g dry wt, supporting their biogenetic conversion. Micropropagated plantlets produced four times more alkaloids (27.6 ± 3.1 mg/g dry wt) than greenhouse plants. Plantlet roots yielded 3, 4, 8 and the glucoindole alkaloids 3α-dihydrocadambine (9) and dolichantoside (10), the last one not previously found in Uncaria.     

First evaluation of the cookie-cutter sharks (<Emphasis Type="Italic">Isistius sp.</Emphasis>) predation pattern on different cetacean species in Martinique

Cookie-cutter sharks (Isistius sp.) are small squaloid sharks that live in tropical and sub-tropical oceans. Their name comes from their unique tactic of feeding, which enables them to parasitize marine mega-fauna, like cetaceans. Due to their morphological and anatomical characteristics, they are responsible of crater-like wounds on the skin of marine mammals. Little is known on Isistius sp. around the globe especially in Martinique, which represents a potential habitat. The main goal of this study was to assess the impact of cookie-cutter sharks on cetaceans by determining (1) seasonal changes in the occurrence of bites, (2) intra- and interspecific differences in frequencies and locations of bites among the different species of cetaceans, and (3) link behavior patterns of both cookie-cutter sharks and cetaceans. Data were collected from a 3-year photo-identification database of Cetaceans in Caribbean coast of Martinique. 431 wounds of various stages on 396 individuals from nine species of marine mammals were recorded. Results did not show any significant variation in the occurrence of wounds between seasons. Intermediate state was more important, most injuries were observed on the SCF (Superior Central Flank) (62.40%) and in a lesser extent on young individuals (3.25%). The predation of cookie-cutter sharks on different cetacean species has been confirmed consistently in Martinique. Further studies are required with both scientists and fishermen to better understand their specific role in this marine ecosystem.     

A new species of <Emphasis Type="Italic">Vanilla</Emphasis> (Orchidaceae: Vanilloideae) from São Paulo,Brazil

A new orchid species, Vanilla paludosa, native to marshy forests close to cerrado vegetation in the state of São Paulo, Brazil, is described and illustrated. The relationship of V. paludosa to other species of the genus is discussed.     

Isolation and Antibiotic Screening of Fungi from a Hydrothermal Vent Site and Characterization of Secondary Metabolites from a <Emphasis Type="Italic">Penicillium</Emphasis> Isolate

Five new compounds were isolated from Penicillium sp. Y-5-2 including an austin derivative 4, four isocoumarins 9, 11, 12, and 13, together with two known isocoumarins 8 and 10, and six known austin derivatives 1, 2, 3, 5, 6, and 7 and one phenol 14. Their structures and relative configurations were established by spectroscopic means. The absolute configurations of 4, 11, and 13 were defined mainly by comparison of quantum chemical TDDFT calculated and experimental ECD spectra. The cyclization of the pentan-2-ol pendant at C-3 in compound 13 allowed the assignment of a new 2,3,4,4a,6,10b-hexahydro-1H-benzo[c]chromene isocoumarin skeleton. New compounds 9, 11, and 13 revealed inhibitory activities against E. coli at MIC values around 32 μg/mL. The known compound 14 showed potent antibiotic activity against Staphylococcus aureus and Bacillus subtilis with MIC values 8 and 2 μg/mL, respectively, with no cytotoxicity when tested in vitro. A rapid and efficient technique for selecting antibiotic fungal strain among eight marine-derived fungi was also described.     

Design and synthesis of an indol derivative as antibacterial agent against <Emphasis Type="Italic">Staphylococcus aureus</Emphasis>

Several indole derivatives with antibacterial activity have been prepared using different protocols; however, some require special reagents and conditions. The aim of this study involved the synthesis of some indole derivatives using estrone and OTBS-estrone as chemical tools. The synthesis of the indole derivatives involves reactions such as follows: (1) synthesis of two indol derivatives (4 or 5) by reaction of estrone or OTBS-estrone with phenylhydrazine in medium acid; (2) reaction of 4 or 5 with 6-cloro-1-hexyne in medium basic to form two hexynyl-indol (7 or 8); (3) preparation of indol-propargylic alcohol derivatives (10 or 11) by reaction of benzaldehyde with 7 or 8 in medium basic; (4) synthesis of indol-aldehydes (12 or 13) via oxidation of 10 or 11 with DMSO; (5) synthesis of indeno-indol-carbaldehyde (15 or 16) via alkynylation/cyclization of 12 or 13 with hexyne in presence of copper(II); (6) preparation indeno-indol-carbaldehyde complex (19 or 20) via alkynylation/cyclization of 12 or 13 with 1-(hex-5-yn-1-yl)-2-phenyl-1H-imidazole. The antibacterial effect exerted by the indol-steroid derivatives against Streptococcus pneumoniae and Staphylococcus aureus bacteria was evaluated using dilution method and the minimum inhibitory concentration (MIC). The results showed that only the compound 19 inhibit the growth bacterial of S. aureus. In conclusion, these data indicate that antibacterial activity of 19 can be due mainly to functional groups involved in the chemical structure in comparison with the compounds studied.