Los Tintinidos (Protozoa: Ciliata) del mar peruano y sus relaciones con el fenómeno El Niño

Se ha estudiado la composición, abundancia y distribución de las especies de Tintinida (Protozoa: Ciliata) en relación con las condiciones ambientales, entre 1982 y 1985. Se han identificado 54 especies pertenecientes a 30 géneros y 12 familias. Se utilizaron 901 muestras colectadas con red estándar de fitoplancton en 15 cruceros realizados por el Instituto del Mar del Perú, entre la primavera de 1982 y el verano de 1985, a lo largo del litoral peruano, entre Puerto Pizarro (04' S) e llo (18°S). Además se estudiaron 216 muestras de agua obtenidas con botellas Niskin en 7 estaciones distribuidas a lo largo del perfil Callao (12° S) y a profundidades de 0, 10, 25 y 50 m. Las mayores densidades se presentaron en el verano de 1985, por las especies: Eutintinnus tubulosus, Hellicostomella longa y H. subulata, época considerada como normal de acuerdo a las condiciones oceanográficas. La composición por especies cambia con la distancia de la costa. Dentro de las 30 mn predominaron H. longa y H. subulata; y en la región oceánica: Eutintinnus similis, Oadayiella ganymedes y X ystonella treforti, especies de aguas subtropicales superficia­les. En la distribución vertical, las mayores concentraciones se encontraron entre los O y 25 m de profundidad, muy cerca de la costa.

Propagação vegetativa de cedo-australiano (Toona ciliata M. Roemer) por miniestaquia

O método de propagação usual do cedro-australiano (Toona ciliata) é via seminal, entretanto a oferta sazonal das sementes e sua curta viabilidade ao longo do tempo representam um problema para a produção contínua de mudas destinadas à implantação de povoamentos. Este trabalho foi conduzido com o objetivo de avaliar a viabilidade da propagação vegetativa da espécie por miniestaquia e a necessidade da aplicação de acido indolbutírico (AIB) para o enraizamento das miniestacas. A partir de um banco de estacas de origem seminal, foram obtidas brotações para produção de mudas clonais, em três diferentes épocas de coleta (2,5; 4,5; e 5,5 meses após a recepa das mudas). Antes do estaqueamento, as miniestacas tiveram suas bases imersas em quatro concentrações de AIB (0; 1.500; 3.000; e 4.500 mg L-1). Durante o experimento, obtiveram-se 100% de sobrevivência das minicepas e das miniestacas. Houve 100% de enraizamento das miniestacas nas três coletas, não ocorrendo diferença no comprimento de raízes em função das doses de auxina aplicadas. Quanto maior o intervalo entre as coletas e quanto maiores as brotações que originaram as miniestacas, maior a velocidade de crescimento das mudas. Miniestacas de cedro-australiano possuem capacidade de enraizamento, e mudas recepadas apresentam brotação, possibilitando a clonagem da espécie pelo processo de miniestaquia.

Efeito do volume de tubetes na produção de mudas de Calophyllum brasiliense e Toona ciliata

A demanda por informações silviculturais de espécies florestais alternativas para reflorestamentos com fins econômicos, entre as quais incluem os métodos de produção de mudas, tem aumentado nos últimos anos. Neste trabalho, avaliou-se a influência de volumes de tubetes, com dimensões de 115, 180 e de 280 cm³, no crescimento de mudas de guanandi (Calophyllum brasiliense Cambess.) e cedro-australiano (Toona ciliata M. Roem. var. australis (F. Muell.) Bahadur). O substrato utilizado foi composto por uma mistura de 80% de substrato comercial e 20% de argila. Foram avaliados o diâmetro de colo e a altura das mudas aos 60, 90, 120 e 150 dias após a repicagem. Nessa última ocasião, determinou-se também o peso de massa seca da parte aérea, do sistema radicular e total, bem como o Índice de Qualidade de Dickson. Houve efeito do volume do tubete sobre as características das mudas, sendo o cedro-australiano a espécie mais responsiva. Conclui-se que para o guanandi o tubete mais indicado é o de 180 cm³ e para o cedro-australiano, o de 280 cm³.

Biossólido como substrato para produção de mudas de Toona ciliata var. australis

O êxito de plantios florestais não está ligado unicamente à espécie utilizada, mas depende diretamente do tipo de recipiente, da qualidade das sementes e do substrato utilizado. O objetivo do trabalho foi avaliar a influência do biossólido como substrato na produção de mudas de cedro-australiano (Toona ciliata). O experimento foi realizado em casa de sombra do Viveiro Florestal/CCA/UFES. O delineamento experimental utilizado foi o inteiramente casualizado, sendo constituído de seis tratamentos contendo biossólido, em proporções decrescentes, associado com terra de subsolo e dois tratamentos sem o uso de biossólido (esterco bovino + terra de subsolo e substrato comercial, respectivamente), com oito repetições. No geral, os melhores resultados para as características morfológicas analisadas foram obtidos com a utilização de 100 a 70% de biossólido na composição do substrato. Portanto, o biossólido pode ser considerado adequado para o crescimento de mudas de Toona ciliata o que demonstra uma alternativa viável de disposição final desse resíduo.

Biomassa, teores de nutrientes, espilantol e atividade antioxidante em plantas de jambu (Acmella ciliata Kunth) sob adubações mineral e orgânica

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Population dynamics of the Sycamore Lace Bug (Corythucha Ciliata, Say, Heteroptera: Tingidae) in Hungary

Based on the observation of more than 10 000 leaves of plane trees, four populations of Corythucha ciliata (Say, 1832) (Heteroptera: Tingidae) are investigated. After having introduced some parameters derived from the data, we draw spatial-temporal patterns and describe the seasonal population dynamics of Corythucha ciliata. Amongst others, the temporal change of the density of population, the state plane of larvae–adults, the inclination to accumulate, and the intraspecific competition are examined. Population and biomass dynamics is characterized for populations with and without limited nutrient source in case of different weather circumstances and effects.

The effect of climate change on the population of sycamore lace bug (Corythuca ciliata, Say) based on a simulation model with phenological response

Climate change affects on insect populations in many ways: it can cause a shift in geographical spread, abundance, or diversity, it can change the location, the timing and the magnitude of outbreaks of pests and it can define the phenological or even the genetic properties of the species. Long-time investigations of special insect populations, simulation models and scenario studies give us very important information about the response of the insects far away and near to our century. Getting to know the potential responses of insect populations to climate change makes us possible to evaluate the adaptation of pest management alternatives as well as to formulate our future management policy. In this paper we apply two simple models, in order to introduce a complex case study for a Sycamore lace bug population. We test how the model works in case the whether conditions are very different from those in our days. Thus, besides we can understand the processes that happen in present, we can analyze the effects of a possible climate change, as well.

Floral development in the tribe Cedreleae (Meliaceae, sub-family Swietenioideae): Cedrela and Toona

Background and Aims Floral development of Cedrela and Toona, the genera comprising the basal tribe Cedreleae of the sub-family Swietenioideae of Meliaceae, is described. The focus was on three endangered, ecologically and economically important species: Cedrela fissilis, Cedrela odorata and Toona ciliata. The aims of the study were to characterize the patterns of floral development in the tribe and to establish apomorphic and plesiomorphic floral characters in relation to other taxa within the family based on the current molecular phylogeny of Meliaceae. Methods A detailed floral structural and developmental study was completed using both scanning electron microscopy and visualization of microtome sections with a light microscope. Key Results Twelve floral developmental stages were identified. The initial development of the pentamerous flowers of both Toona and Cedrela is strikingly similar. The morphological differences observed between them are due to differential patterns of organ elongation and adnation/connation occurring late in development. Additionally, the formation of functionally male and female flowers was found to occur at specific positions within the inflorescence. Conclusions Due to the basal position of the tribe Cedreleae in the phylogeny of Meliaceae, functionally either male or female pentamerous flowers and the presence of (at least partially) free stamens may be considered plesiomorphic traits within the family. In contrast, sympetaly and the absence of nectaries in Cedrela species are synapomorphies.

The subfamily Aephnidiogeninae Yamaguti, 1934 (Digenea: Lepocreadiidae), its status and that of the genera Aephnidiogenes Nicoll, 1915, Holorchis Stossich, 1901, Austroholorchis n g, Pseudaephnidiogenes Yamaguti, 1971, Pseudoholorchis Yamaguti, 1958 and N

The status of all of the putative member genera of the subfamily Aephnidiogeninae is reconsidered, based mainly on the morphology of the terminal genitalia, Aephnidiogenes Nicoll, 1915 is the only genus retained in the Aaephnidiogeninae. Aephnidiogenes major Yamaguti, 1934 from Diagramma labiosum from the southern Great Barrier Reef is redescribed with particular reference to the terminal genitalia, and is shown to lack a true cirrussac, a condition considered to be diagnostic of the Aephnidiogeninae. Holorchis Stossich, 1901 is placed in the subfamily Lepidapedinae. Holorchis pycnoporus Stossich, 1901 from Pagellus acarne from off Spanish Sahara and from Diplodus vulgaris from off Italy and H. legendrei Dollfus, 1946 from Sparodon durbanensis and D. sargus from off eastern Cape Province, South Africa and from Pagellus erythrinus from the Adriatic Sea and Italy are studied and illustrated. The terminal genitalia of H. pycnoporus are found to be enigmatic, but those of H. legendrei are found to fit clearly into the 'Lepidapedon-like' pattern. A new genus Austroholorchis is erected in the Lepidapedinae, with A. sprenti (Gibson, 1987) n. comb. as the type-species. Its diagnostic features are its ani, infundibuliform oral sucker and the position of the ovary at about mid-level of the uterus. A. sprenti is illustrated, its hosts in Queensland waters being Sillago maculata, S, analis and S. ciliata. A, levis n. sp. is described from Sillago bassensis from south-western Western Australia. The genus Pseudaephnidiogenes Yamaguti, 1971 is placed in the Lepidapedinae. P. rhabdosargi (Prudhoe, 1956) from Rhabdosargus sarba from off Natal, South Africa is illustrated and the terminal genitalia of P. rhabdosargi from R. sarba and from R. holubi from off eastern Cape Province and Pseudaephnidiogenes vossi Bray, 1985 from Caffrogobius nudiceps from off eastern Cape Province, South Africa are illustrated. The genus Pseudoholorchis Yamaguti, 1958 is placed in the subfamily Lepocreadiinae. The terminal genitalia of P. pulcher (Manter, 1954) from Latridopsis ciliaris from New Zealand are illustrated, The genus Neolepocreadium Thomas, 1960 is placed in the Lepocreadiidae.

Postlepidapedon Zdzitowiecki, 1993 and Gibsonivermis n g (Digenea: Lepocreadiidae) from fishes of the southern Great Barrier Reef, Australia, and their relationship to Intusatrium Durio & Manter, 1968

The genus Intusatrium Durio & Manter, 1968 is redefined based on a re-examination of paratypes of the type-species, I. robustum Durio & Manter, 1968, and is considered monotypic with characteristic terminal genitalia: internal seminal vesicle elongate tubular, with rather thick wall, divided by slight change in wall thickness into longer proximal and shorter distal region; pars prostatica subcylindrical; ejaculatory duct relatively short, with wrinkled/wall. The genus Postlepidapedon Zdzitowiecki, 1993 is redefined and Intusatrium secundum Durio & Manter, 1968 is attributed to it as a new combination. Postlepidapedon secundum n. comb. is redescribed from a paratype and new material from Choerodon graphicus. P. spissum n. sp. from Choerodon venustus, C. cyanodus, C. fasciatus and C. schoenleinii is recognised on the basis of its thick-walled internal seminal vesicle. I! uberis n. sp. from Choerodon schoenleinii and C. venustus is distinguished by the shape and contents of the cirrus-sac with narrow, convoluted internal seminal vesicle, large vesicular pars prostatica and short, muscular ejaculatory duct. A new genus, Gibsonivermis, erected for Intusatrium berryi Gibson, 1987, is characterised by the elongate narrow cirrus-sac and a uroproct. G. berryi n. comb. is redescribed from Sillago ciliata, S. maculata and Sillago sp.