Diferenças entre Chenopodium quinoa e a planta daninha Chenopodium album

A experimentação pioneira com Chenopodium quinoa Willd tem demonstrado sua adaptabilidade à produção de grãos no cerrado. Seus frutos, do tipo aquênio, são cilíndricos, achatados e germinam rapidamente na presença de umidade, após a maturação fisiológica. Na fase inicial do seu desenvolvimento, a quinoa pode ser confundida com a planta daninha Chenopodium album, conhecida no Brasil como ançarinha-branca. As diferenças básicas entre as duas espécies se tornam mais visíveis após o florescimento: ramificação profusa, com rácemos axilares e terminais em C. album, em contraste com C. quinoa, na qual as panículas são terminais, à semelhança do sorgo; o pericarpo é claro e contrasta com o preto em C. album. A quinoa BRS Piabiru, primeiro cultivar para o Brasil, apresenta plantas com 190 cm, nas quais a panícula ocupa 45 cm; maturação fisiológica aos 145 dias; resistência ao acamamento; peso de grãos de 2,42 g 1.000-1; rendimento de 2,8 t ha-1; e biomassa total de 6,6 t ha-1. As sementes de C. album são muito pequenas (0,52 g 1.000-1), germinam gradativamente e permanecem no solo por muitos anos, infestando os cultivos. As diferenças no número de cromossomos, impedindo a polinização cruzada entre as duas espécies e as morfológicas, detectadas na experimentação, mostram que estas são distinguíveis e asseguram que a quinoa apresenta características de adaptação ao cultivo comercial, contrapondo-se às características de invasora em C. album.

Caracterização química das plantas aquáticas coletadas no reservatório de Salto Grande (Americana-SP)

O objetivo deste trabalho foi caracterizar a constituição química das espécies de plantas aquáticas Brachiaria arrecta, Eichhornia crassipes, Pistia stratiotes e Salvinia auriculata - encontradas no reservatório da usina hidrelétrica de Salto Grande, em Americana-SP - de forma a fornecer subsídios para futuras avaliações sobre o comportamento da biomassa dessas espécies em local de descarte ou no próprio reservatório. As amostras de plantas foram coletadas no dia 16.4.2002, sendo desidratadas em estufa de circulação forçada de ar a 60 ºC. B. arrecta apresentou os menores teores médios de macro e micronutrientes e o maior teor médio de elementos pesados na matéria seca, em relação às demais espécies. A relação C/N das espécies E. crassipes, P. stratiotes e S. auriculata apresentou valores próximos. Não foi detectada, em nenhuma das espécies estudadas, a presença dos elementos molibdênio, prata, chumbo e mercúrio.

Dinâmica do herbicida amicarbazone (Dinamic) aplicado sobre palha de cana-de-açúcar (Saccarum officinarum)

O objetivo deste trabalho foi estudar a dinâmica do herbicida amicarbazone (Dinamic) aplicado sobre palha de cana-de-açúcar deixada sobre o solo, em sistema de cana crua. Três ensaios foram realizados para avaliar a dinâmica desse herbicida aplicado sobre diferentes quantidades de palha de cana-de-açúcar, em diferentes intervalos de tempo e volumes de simulação de chuvas após aplicação do herbicida. No primeiro ensaio, foi avaliada a interceptação do herbicida por 0, 1, 2,5, 5, 7,5, 10, 15 e 20 t de palha de cana-de-açúcar ha-1. A lixiviação do herbicida em 5, 10, 15 e 20 t de palha ha-1 foi avaliada sob simulação de chuva de 2,5, 5, 10, 15, 20, 35 e 65 mm, um dia após a aplicação (DAPC) do segundo ensaio. As chuvas foram acumulativas, aplicando-se de 2,5 em 2,5 mm. No terceiro ensaio, foi avaliado o efeito dos intervalos de tempo entre a aplicação do herbicida e a primeira chuva na lixiviação do herbicida Dinamic (0, 1, 7, 15 e 30 dias) em 10 t de palha ha-1, em função das mesmas precipitações simuladas no segundo ensaio. Nos segundo e terceiro ensaios foi realizada uma simulação de 20 mm em intensidade de 115 mm h-¹ aos 7 e 14 dias após as primeiras chuvas (DAPC). Os resultados obtidos no segundo e terceiro ensaios foram ajustados pelo modelo de Mitscherlich (Y = a * (1-10-c * (b + x))). A quantificação do herbicida foi realizada por cromatografia líquida de alta eficiência. Quantidades de palha iguais ou superiores a 5 t ha-1 apresentam interceptação quase que total do herbicida no momento da aplicação, sendo nula a transposição. Com o aumento da quantidade de palha, ocorreu diminuição na quantidade de herbicida lixiviado pela ação da chuva simulada, principalmente para valores de 15 e 20 t de palha de cana-de-açúcar ha-1. Quanto maior o intervalo de tempo entre a aplicação do herbicida e a primeira chuva, menor é a lixiviação total do produto. Em relação às chuvas aos 7 e 14 DAPC, no segundo e terceiro ensaios, foram observadas pequenas quantidades extraídas do herbicida, considerando-se que grande parte do amicarbazone foi lixiviada com as primeiras chuvas, que indicaram que os primeiros 20 mm de chuva simulada foram importantes para lixiviação da maior parte do amicarbazone (Dinamic) retido pela palha no momento da aplicação.

Caracterização física, química e nutricional dos frutos da Aninga

Montrichardia linifera, conhecida popularmente como aninga, pertence à família Araceae e forma grandes populações às margens dos rios e igarapés da Amazônia, principalmente de águas brancas (barrentas). Seus frutos fazem parte da dieta alimentar de peixes, tartarugas e de grandes herbívoros, como peixe-boi e búfalo, havendo, portanto, a hipótese de seu aproveitamento na nutrição animal. Entretanto, apesar de sua vasta distribuição na paisagem amazônica, não existem dados na literatura sobre a composição nutricional desses frutos. Com os objetivos de avaliar o seu potencial nutricional e contribuir para o conhecimento dessa espécie, foi realizada, neste trabalho, a caracterização física, química e nutricional dos frutos. A infrutescência pesa em média 500 g, com um conjunto de aproximadamente 80 frutos. O seu valor nutritivo se resume, basicamente, ao seu valor energético (≅ 350 kcal), devido principalmente ao teor de carboidratos (≅ 80%), possuindo baixo valor proteico (< 0,5%). As concentrações de manganês (≅ 1.800 mg kg-1) foram consideradas tóxicas, extrapolando o limite máximo tolerável em nutrição de bubalinos (1.000 mg kg-1).

Effects of early compost application on no-till organic soybean

Weed control has always been an important issue in agriculture. With the advent of no-till systems, soil erosion was reduced but herbicide use was increased. Organic no-till systems try to adjust reduced erosion to the no use of herbicides. Nevertheless, this adjustment is limited by the cost of mechanical weed control. This cost may be reduced by improved cultural weed control with cover crops mulches. In this paper we report a study on the application of compost manure on an oats winter cover crop, preceding soybean, instead of on the soybean summer crop. Treatments comprised a control without compost manure, and compost manure doses of 4 and 8 Mg ha-1 applied either on oats in winter or soybean in summer, organized in a randomized block design, with five replications. In summer, plots were split into weed-controlled or not controlled subplots. The timing of application and the manure doses did not affect the oats biomass or the soybean performance. However, in summer, without water stress, the application of manure at 8 Mg ha-1 directly on soybean has reduced weed biomass in this crop.

Polygala extraaxillaris: oxidative stress in Brachiaria decumbens mediated by volatile oils

The volatile oils extracted from the roots of Polygala extraaxillaris were analyzed to assess whether they increase oxidative stress in Brachiaria decumbens var. Piatã, as well as to assess their effect on cellular division and cytotoxicity in laboratory. Six concentrations were used (0%, 0.35%, 0.65%, 1.25%, 0.65%, and 5.0%) with four repetitions of 25 seeds. The substance 1-(2-hydroxyphenyl) - ethanone was identified as the major constituent of the volatile oils. The results showed that the highest concentrations of the oils resulted in an increase in the oxidative stress in B. decumbens, as well as alteration in germination and growth, with a consequent reduction in the process of cellular division, causing changes in the growth standard and antioxidant defense.

Host suitability of weeds and forage species to root-knot nematode meloidogyne graminicola as a funcion of irrigation management

The irrigated rice production can be limited by various phytopathogenic agents, including root-knot nematodes (Meloidogyne spp.). Thus, the aim of this research was to check the host suitability of plant species most often found off-season and during rice cultivation, to root-knot nematode Meloidogyne graminicola, under two irrigation managements. Two experiments were conducted in a completely randomized design. In the first experiment seven plant species that occur in an area of rice cultivation, in fallow, off-season were evaluated. For the second experiment nine weed species infesting the irrigated rice culture were tested in rainfed and flooding conditions. The sixteen species, kept individually in pots with sterilized substrate, were inoculated with 5,000 eggs and second stage juveniles (J2) of nematode. BRS 410 IRGA rice plants inoculated with M.graminicola were used as control. Two months after inoculation, the root system of each plant was evaluated for number of galls and nematode reproduction factor. It was verified that the species of off-season of rice cultivation Sida rhombifolia, Raphanus raphanistrum, Spergula arvensis, Lotus corniculatus and Trifolium repens, and, during the cycle of rice cultivation, Aeschynomene denticulata, Leersia hexandra, are immune to nematode. The plant species off-season, Avena strigosa and Lolium multiflorum and of cultivation, Alternanthera philoxeroides, red rice, Echinochloa crusgalli, Cyperus difformis, Cyperus esculentus, Cyperus iria and Fimbristylis miliacea would behave as hosts of M.graminicola, mostly under rainfed conditions.

Shikimate accumulation, glyphosate absorption and translocation in horseweed biotypes

In Brazil, few research works on mechanisms of weed resistance to glyphosate have been conducted so far. Therefore, this research aimed to study analytical procedures determining the relation between the concentration of plant shikimate after glyphosate application and the plant resistance to this herbicide; and evaluate the glyphosate absorption and translocation into two resistant ® and susceptible (S) horseweed biotypes to glyphosate. Horseweed plants with nine true leaves received glyphosate (720 g a.e. ha-1), and 2, 3, 4, 7 and 10 days after application (DAA) the concentration of shikimic acid was measured by HPLC. In another experiment, plants were treated with radiolabeled glyphosate (14C) (1.456 MBq mmol-1 specific activity) and radioactivity was measured 4, 8, 24, 48 and 72 hours after treatment (HAT) by liquid scintillation spectrometry. The shikimate concentration in plants increased 16,351.14 and 7,892.25 mg kg-1 of dry weight, for R and S plants respectively, at seven DAA. Therefore, the procedure for quantification of shikimic acid was suitable for R and S plants differentiation to glyphosate, indicating that the R population is actually resistant to glyphosate. On average, 98% of glyphosate applied was absorbed by the studied biotypes, at 72 HAT. Around 68% of the absorbed radioactivity remained on the biotypes leaves treated, the S biotype showing the highest translocation. Therefore, the R biotype resistance mechanism studied is associated to the differential translocation.

Eunotiaceae (Eunotiales, Bacillariophyta) em ambientes lacustres na Planície Costeira do Sul do Brasil

O estudo da família Eunotiaceae em diferentes ambientes (lagoas, banhados e açude) na Planície Costeira do Rio Grande do Sul foi realizado no outono e primavera de 2003. Foram identificados 26 táxons específicos e infra-específicos, um pertencente ao gênero Actinella e 25 a Eunotia. A maior riqueza de espécies de Eunotia foi registrada nos banhados, onde a vegetação marginal foi mais abundante e as águas mais ácidas (pH 4,3 e 5,4). Eunotia bilunaris (Ehr.) Souza, E. tridentula Ehr. var. tridentula, E. vumbae Choln., E. yberai Freng. e E. zygodon Ehr. tratam-se de primeiras citações para a Planície Costeira do sul do Brasil. As espécies são descritas, comentadas e ilustradas em microscopio óptico (MO) e/ou em microscópio eletrônico de varredura (MEV).

Pituitary glycoprotein hormone a-subunit secretion by cirrhotic patients

Secretion of the a-subunit of pituitary glycoprotein hormones usually follows the secretion of intact gonadotropins and is increased in gonadal failure and decreased in isolated gonadotropin deficiency. The aim of the present study was to determine the levels of the a-subunit in the serum of patients with cirrhosis of the liver and to compare the results obtained for eugonadal cirrhotic patients with those obtained for cirrhotic patients with hypogonadotropic hypogonadism. Forty-seven of 63 patients with cirrhosis (74.6%) presented hypogonadism (which was central in 45 cases and primary in 2), 7 were eugonadal, and 9 women were in normal menopause. The serum a-subunit was measured by the fluorimetric method using monoclonal antibodies. Cross-reactivity with LH, TSH, FSH and hCG was 6.5, 1.2, 4.3 and 1.1%, respectively, with an intra-assay coefficient of variation (CV) of less than 5% and an interassay CV of 5%, and sensitivity limit of 4 ng/l. The serum a-subunit concentration ranged from 36 to 6253 ng/l, with a median of 273 ng/l. The median was 251 ng/l for patients with central hypogonadism and 198 ng/l for eugonadal patients. The correlation between the a-subunit and basal LH levels was significant both in the total sample (r = 0.48, P<0.01) and in the cirrhotic patients with central hypogonadism (r = 0.33, P = 0.02). Among men with central hypogonadism there was a negative correlation between a-subunit levels and total testosterone levels (r = 0.54, P<0.01) as well as free testosterone levels (r = -0.53, P<0.01). In conclusion, although the a-subunit levels are correlated with LH levels, at present they cannot be used as markers for hypogonadism in patients with cirrhosis of the liver.

Immunization by subcutaneous implants of polyester-polyurethane sponges coupled with antigen

A new protocol is described for immunization of outbred Swiss mice. The procedure is based on subcutaneous implantation of antigen-coupled polyester-polyurethane sponges cut into disks of 10 mm in diameter vs 2 mm in thickness. Antigen coupling was performed by overnight incubation of the sponge with a solution of ovalbumin (Ova) (2 mg/ml) diluted in sodium carbonate buffer, pH 9.6. The amount of ovalbumin that was taken up by the sponge was between 71.4 to 82.5 µg. This was estimated by comparing the Ova absorbance at 280 nm in coating buffer solutions before and after incubation. To compare the efficiency of the proposed method, experimental groups immunized with the antigen in the presence of adjuvants (10 µg in Al(OH)3 or 100 µg in complete Freund's adjuvant (CFA)) were run in parallel. The data obtained after the 3rd week of immunization indicate that both cellular and humoral immune responses were achieved. These were assayed by antigen-induced footpad swelling and ELISA (specific antibodies), respectively. The levels of both immune responses elicited were similar to the responses observed in mice immunized with ovalbumin in the presence of Al(OH)3. The method might represent an advantage when immunizing with pathogenic antigens. Preliminary experiments have suggested that the antigen remains immobilized or bound to the sponge for a long period of time, since there is an increment on the cell population inside the sponges after boosting the animals. If so, the undesirable effects of immunization would be reduced.

Detection of cytomegalovirus infections by PCR in renal transplant patients

Cytomegalovirus (CMV) is the single most important infectious agent affecting recipients of organ transplants. To evaluate the incidence and the clinical importance of CMV infection in renal transplants in Brazil, 37 patients submitted to renal allograft transplants were tested periodically for the presence of cytomegalovirus DNA in urine using the polymerase chain reaction (PCR), and for the presence of IgM and IgG antibodies against CMV by enzyme-linked immunosorbent assay (ELISA) and indirect immunofluorescence (IIF). The PCR-amplified products were detected by gel electrophoresis and confirmed by dot-blot hybridization with oligonucleotide probes. Thirty-two of the 37 patients (86.4%) were positive by at least one of the three methods. In six patients, PCR was the only test which detected the probable CMV infection. Ten patients had a positive result by PCR before transplantation. In general, the diagnosis was achieved earlier by PCR than by serologic tests. Active infection occurred more frequently during the first four months after transplantation. Sixteen of the 32 patients (50%) with active CMV infection presented clinical symptoms consistent with CMV infection. Five patients without evidence of active CMV infection by the three tests had only minor clinical manifestations during follow-up. Our results indicate that PCR is a highly sensitive procedure for the early detection of CMV infection and that CMV infection in renal transplant patients is a frequent problem in Brazil.

Possible involvement of A1 receptors in the inhibition of gonadotropin secretion induced by adenosine in rat hemipituitaries in vitro

We investigated the participation of A1 or A2 receptors in the gonadotrope and their role in the regulation of LH and FSH secretion in adult rat hemipituitary preparations, using adenosine analogues. A dose-dependent inhibition of LH and FSH secretion was observed after the administration of graded doses of the R-isomer of phenylisopropyladenosine (R-PIA; 1 nM, 10 nM, 100 nM, 1 µM and 10 µM). The effect of R-PIA (10 nM) was blocked by the addition of 8-cyclopentyltheophylline (CPT), a selective A1 adenosine receptor antagonist, at the dose of 1 µM. The addition of an A2 receptor-specific agonist, 5-N-methylcarboxamidoadenosine (MECA), at the doses of 1 nM to 1 µM had no significant effect on LH or FSH secretion, suggesting the absence of this receptor subtype in the gonadotrope. However, a sharp inhibition of the basal secretion of these gonadotropins was observed after the administration of 10 µM MECA. This effect mimicked the inhibition induced by R-PIA, supporting the hypothesis of the presence of A1 receptors in the gonadotrope. R-PIA (1 nM to 1 µM) also inhibited the secretion of LH and FSH induced by phospholipase C (0.5 IU/ml) in a dose-dependent manner. These results suggest the presence of A1 receptors and the absence of A2 receptors in the gonadotrope. It is possible that the inhibition of LH and FSH secretion resulting from the activation of A1 receptors may have occurred independently of the increase in membrane phosphoinositide synthesis.

Signal transduction induced in Trypanosoma cruzi metacyclic trypomastigotes during the invasion of mammalian cells

Penetration of Trypanosoma cruzi into mammalian cells depends on the activation of the parasite's protein tyrosine kinase and on the increase in cytosolic Ca2+ concentration. We used metacyclic trypomastigotes, the T. cruzi developmental forms that initiate infection in mammalian hosts, to investigate the association of these two events and to identify the various components of the parasite signal transduction pathway involved in host cell invasion. We have found that i) both the protein tyrosine kinase activation, as measured by phosphorylation of a 175-kDa protein (p175), and Ca2+ mobilization were induced in the metacyclic forms by the HeLa cell extract but not by the extract of T. cruzi-resistant K562 cells; ii) treatment of parasites with the tyrosine kinase inhibitor genistein blocked both p175 phosphorylation and the increase in cytosolic Ca2+ concentration; iii) the recombinant protein J18, which contains the full-length sequence of gp82, a metacyclic stage surface glycoprotein involved in target cell invasion, interfered with tyrosine kinase and Ca2+ responses, whereas the monoclonal antibody 3F6 directed at gp82 induced parasite p175 phosphorylation and Ca2+ mobilization; iv) treatment of metacyclic forms with phospholipase C inhibitor U73122 blocked Ca2+ signaling and impaired the ability of the parasites to enter HeLa cells, and v) drugs such as heparin, a competitive IP3-receptor blocker, caffeine, which affects Ca2+ release from IP3-sensitive stores, in addition to thapsigargin, which depletes intracellular Ca2+ compartments and lithium ion, reduced the parasite infectivity. Taken together, these data suggest that protein tyrosine kinase, phospholipase C and IP3 are involved in the signaling cascade that is initiated on the parasite cell surface by gp82 and leads to Ca2+ mobilization required for target cell invasion.

Proliferative signaling initiated in ACTH receptors

This article reviews recent results of studies aiming to elucidate modes of integrating signals initiated in ACTH receptors and FGF2 receptors, within the network system of signal transduction found in Y1 adrenocortical cells. These modes of signal integration should be central to the mechanisms underlying the regulation of the G0->G1->S transition in the adrenal cell cycle. FGF2 elicits a strong mitogenic response in G0/G1-arrested Y1 adrenocortical cells, that includes a) rapid and transient activation of extracellular signal-regulated kinases-mitogen-activated protein kinases (ERK-MAPK) (2 to 10 min), b) transcription activation of c-fos, c-jun and c-myc genes (10 to 30 min), c) induction of c-Fos and c-Myc proteins by 1 h and cyclin D1 protein by 5 h, and d) onset of DNA synthesis stimulation within 8 h. ACTH, itself a weak mitogen, interacts with FGF2 in a complex manner, blocking the FGF2 mitogenic response during the early and middle G1 phase, keeping ERK-MAPK activation and c-Fos and cyclin D1 induction at maximal levels, but post-transcriptionally inhibiting c-Myc expression. c-Fos and c-Jun proteins are mediators in both the strong and the weak mitogenic responses respectively triggered by FGF2 and ACTH. Induction of c-Fos and stimulation of DNA synthesis by ACTH are independent of PKA and are inhibited by the PKC inhibitor GF109203X. In addition, ACTH is a poor activator of ERK-MAPK, but c-Fos induction and DNA synthesis stimulation by ACTH are strongly inhibited by the inhibitor of MEK1 PD98059.