Espécies de Syrphidae (Diptera) visitantes das flores de Eryngium horridum (Apiaceae) no Vale do Rio Pardo, RS, Brasil

No período entre dezembro de 2001 a dezembro de 2003, realizaram-se coletas com rede entomológica de insetos visitantes das flores de Eryngium horridum (Apiaceae) na Região do Vale do Rio Pardo, RS, Brasil. Esta planta é perene, freqüente em campos secos e apresenta expressiva dispersão. Possui, no Rio Grande do Sul, época de floração entre novembro e janeiro. Foram capturados 1.066 insetos visitantes, destes, 569 Syrphidae. Identificaram-se 60 espécies de Syrphidae, distribuídas em 16 gêneros. O gênero Palpada Macquart, 1834 foi dominante, e Ornidia Lepeletier & Serville, 1828 e Toxomerus Macquart, 1855 abundantes. Das espécies mais freqüentes, Palpada furcata (Wiedemann, 1819) ocupou posição mais elevada. Os sirfídeos apresentaram preferência pelas temperaturas entre 28 e 32ºC, e foram mais freqüentemente coletados entre as 10 e 14 horas, com picos entre as 10 e 11 horas. As fêmeas foram as mais freqüentes. O predomínio de sirfídeos robustos e mais ágeis sobre sirfídeos de menor porte como Toxomerus e Allograpta Osten Sacken, 1875, pode ter sido resultante de competição interespecífica. Eristalinus taeniops (Wiedemann, 1818) é pela primeira vez citada para o Estado do Rio Grande do Sul. A alta diversidade e abundância dos espécimes coletados nas flores de E. horridum são indicadores da importância desta na dieta dos sirfídeos, visto que possui grande número de inflorescências e floração ocorrendo nos meses de baixa oferta de recursos alimentares na área de estudo.

Eryngium foetidum, Petroselinum crispum and Coriandrum sativum: new apiaceae hosts of Oidiopsis taurica in Brazil

Relata-se a infecção natural de plantas de chicória da Amazônia (Eryngium foetidum), coentro (Coriandrum sativum) e salsa (Petroselinum crispum), cultivados em casas de vegetação e campo na Embrapa Hortaliças, Brasília, DF, por Oidiopsis taurica. A provável fonte de inóculo foram plantas doentes de pimentão (Capsicum annuum) e tomate (Lycopersicon esculentum) na casa de vegetação e pimentão no campo.

Behavior of the wild coriander (eryngium foetidum L.) in subtropical conditions

The adaptability of wild coriander (Eryngium foetidum L.) a seasoning and medicinal herb indigenous of the Amazon region was evaluated in a subtropical city of Sao Paulo, Brazil. Germination of seeds was extremely irregular with the first seeds germinating 10 days after the sowing, but the process lasted 90 days. The exploitation of this specie is possible in subtropical conditions without interruption of production but further study on the feasibility elimination of seed and flower are necessary to permit a greater yield of foliage.

Produtividade, compostos bioativos e atividade antioxidante em Eryngium foetidum L

Pós-graduação em Agronomia (Horticultura) - FCA

European phylogeography of the coastal plants Cakile maritima Scop. (Brassicaceae) and Eryngium maritimum L. (Apiaceae)

Linear dispersal systems, such as coastal habitats, are well suited for phylogeographic studies because of their low spatial complexity compared to three dimensional habitats. Widely distributed coastal plant species additionally show azonal and often essentially continuous distributions. These properties, firstly, make it easier to reconstruct historical distributions of coastal plants and, secondly, make it more likely that present distributions contain both Quaternary refugia and recently colonized areas. Taken together this makes it easier to formulate phylogeographic hypotheses. This work investigated the phylogeography of Cakile maritima and Eryngium maritimum, two species growing in sandy habitats along the north Atlantic Ocean and the Mediterranean Sea coasts on two different spatial scales using AFLP data. The genetic structure of these species was investigated by sampling single individuals along most of their distributions from Turkey to south Sweden. On a regional scale the population genetic structure of both species was also studied in detail in the Bosporus and Dardanelles straits, the Strait of Gibraltar and along a continuous stretch of dunes in western France. Additionally, populations of C. maritima were investigated in the Baltic Sea/Kattegat/North Sea area. Over the complete sampling range the species show both differences and similarities in their genetic structure. In the Mediterranean Sea, both species contain Aegean Sea/Black Sea and west Mediterranean clusters. Cakile maritima additionally shows a clustering of Ionian Sea/Adriatic Sea collections. Further, both species show a subdivision of Atlantic Ocean/North Sea/Baltic Sea material from Mediterranean. Within the Atlantic Ocean group, C. maritima from the Baltic Sea and the most northern Atlantic localities form an additional cluster while no such substructure was found in E. maritimum. In all three instances where population genetic investigations of both species were performed in the same area, the results showed almost complete congruency of spatial genetic patterns. In the Aegean/Black Sea/Marmara region a subdivision of populations into a Black Sea, a Sea of Marmara and an Aegean Sea group is shared by both species. In addition the Sea of Marmara populations are more close to the Aegean Sea populations than they are to the Black Sea populations in both cases. Populations from the Atlantic side of the Strait of Gibraltar are differentiated from those on the Mediterranean side in both species, a pattern that confirms the results of the wide scale study. Along the dunes of West France no clear genetic structure could be detected in any of the species. Additionally, the results from the Baltic Sea/North Sea populations of C. maritima did not reveal any geographical genetic pattern. It is postulated that the many congruencies between the species are mainly due to a predominantly sea water mediated seed dispersal in both species and their shared sandy habitat. The results are compared to hypothetical distributions for the last glacial maximum based on species specific temperature requirements. It is argued that in both species the geographical borders of the clusters in the Mediterranean area were not affected by quaternary temperature changes and that the Aegean/Black Sea/Marmara cluster, and possibly the Ionian Sea/Adriatic Sea cluster in C. maritima, is the result of sea currents that isolate these basins from the rest of the sampled areas. The genetic gap in the Strait of Gibraltar between Atlantic Ocean and Mediterranean Sea populations in both species is also explained in terms of sea currents. The existence of three subgroups corresponding to the Aegean Sea, Black Sea and Sea of Marmara basins is suggested to have arisen due to geographical isolation during periods of global sea regressions in the glacials. The population genetic evidence was inconclusive regarding the Baltic Sea cluster of C. Maritima from the wide scale study. The results of this study are very similar to those of an investigation of three other coastal plant species over a similar range. This suggests that the phylo-geographic patterns of widespread coastal plants may be more predictable than those of other terrestrial plants.

Die Verbreitung von Eryngium campestre L., Artemisia campestris L. und Tithymalus Gerardianus Kl. u. Gcke. an der unteren Lippe

Von Dr. Julius Müller

[Eryngium alpinum - Alpendistel]

R. Anheisser

Mannstreu - Eryngium

AR

Mannstreu - Eryngium oliverianum - Eryngium agavifolium

AR

Blütenstände : Dipsacus fullonum - Eryngium giganteum - Echinops ritro

AR

Eryngium - Mannstreu

AR

Eryngium agavifolium - Astrantia maior

AR

Quimiotaxonomía en especies de la Tribu Heliantheae y la Familia Umbeliferas: Probable actividad biológica

La conjugación interdisciplinaria entre la Química y la Taxonomía Vegetal ha dado origen a una nueva disciplina, la Quimiotaxonomía. Esta nueva forma de estudio consiste en aplicar a la clasificación de las plantas los resultados de su análisis químico. Así, la información derivada de los compuestos presentes en los vegetales aporta evidencias que permiten ubicar o reubicar distintos taxones críticos. La evolución de los compuestos químicos y de los aspectos morfológicos está interrelacionada y muchos metabolitos secundarios sirven para confirmar las clasificaciones morfológicas. Sin embargo, en los casos en que las relaciones morfológicas son poco claras, los metabolitos secundarios o marcadores a menudo son pruebas de considerable valor. (...) Para que un compuesto pueda ser utilizado como marcador quimiotaxonómico debe estar presente en el taxón bajo estudio, como así también debe quedar claro su ausencia fuera del mismo. (...) El proyecto tiene dos objetivos fundamentales: a) El aislamiento e identificación de los metabolitos secundarios de especies de la tribu Heliantheae (Asteraceae) con énfasis en los géneros Helianthus y Viguiera y en especies de la familia Umbeliferas , género Eryngium . En ambas familias se ha demostrado que las relaciones morfológicas son poco claras, por lo que la información derivada de los compuestos presentes en los vegetales pueden aportarnos evidencias que permitan ubicar o reubicar distintos taxones críticos. (...) b) La determinación de la bioactividad de los metabolitos secundarios presentes en las especies mencionadas precedentemente. En trabajos anteriores hemos determinado que algunos compuestos obtenidos e identificados pueden ser repelentes de insectos o inhibir el crecimiento de plantas. Por esta razón, se proseguirá con el ensayo sobre los extractos completos y sobre compuestos puros. En algunos casos la purificación será guiada por la mayor o menor actividad biológica de los extractos y fracciones obtenidas. También se recurrirá a su modificación estructural con el objetivo de establecer una relación estructura-actividad.

Revisão taxonômica de Kanaima Distant (Hemiptera, Cercopidae, Ischnorhininae)

Kanaima Distant, 1909 é revisado, sendo suas espécies descritas e redefinidas. Este trabalho ressalta os caracteres taxonomicamente importantes das espécies de Kanaima, como os da morfologia externa e da genitália. Quatro espécies são reconhecidas como válidas: K. katzensteinii (Berg, 1879), K. fluvialis (Lallemand, 1924), K. fusca (Lallemand, 1927) comb. nov., e K. nigra sp. nov. (Brasil, RS). Os nomes Monecphora fluvialis var. lateralis Lallemand, 1924 e Monecphora fluvialis var. bipunctata Lallemand, 1924 são sinonimizados sob Kanaima fluvialis. Quatro espécies incluídas em Kanaima são transferidas para Mahanarva: M. (Ipiranga) vittata (Walker, 1851) comb. nov., M. (Ipiranga) fortunata (Lallemand, 1924) comb. nov., M. (Mahanarva) radiata (Walker, 1851) comb. nov. e M. (Mahanarva) dubia (Stancik & Cavichioli, 2003) comb. nov. Pachypterinella Lallemand, 1927 sin. nov.