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ABSTRACT: In micropropagation, potassium nitrate (KNO3), an ACS reagent grade chemical, used in the preparation of growing mediums is expensive and its procurement depends on bureaucratic procedures, as it is controlled by the Brazilian Army. This research to assessed the effect of replacing the ACS KNO3 for a commercially available fertilizer (KNO3- based) on the micropropagation of the prickly pear cactus (Opuntia stricta (Haw.) Haw. cv. Elephant Ear. Treatments used six different fertilizer concentrations (0, 0.5, 1, 1.5, 2 and 2.5 g L-1) and a control consisting of 1.9 g L-1 KNO3, as shown in the MS salts. The survival, size and number of sprouts and the value of fresh biomass were evaluated. After seedling acclimation, we assessed the survival, number of sprouts, length, and number of roots, racket formation, average fresh biomass mass, macronutrient absorption and morphological changes of the seedlings. Explants inoculated with fertilizers at concentrations of 0.0; 2.0 and 2.5 g L-¹ did not grow. The response of explants at concentrations of 0.5 and 1.5 g L-1 of the fertilizer were the same as those developed in a KNO3 medium, and at a concentration of 1.0 g L-1, in all variables, the means were higher than those of the control medium. Therefore, it showed the feasibility of using fertilizers in the in vitro cultivation of the prickly pear cactus, which may remove bureaucratic barriers and reduce product costs by 99.12%.
RESUMO: Na micropropagação, o nitrato de potássio (KNO3), reagente puro para análise (P.A.), utilizado no preparo dos meios de cultura, possui custo elevado e a sua aquisição depende de trâmites burocráticos, por se tratar de substância controlada pelo Exército Brasileiro. O objetivo deste trabalho foi avaliar o efeito da substituição do KNO3 P.A. por fertilizante comercial (com fonte de KNO3), encontrado livremente no comércio, na micropropagação de palma (Opuntia stricta (Haw.) Haw. cv Orelha de Elefante. Os tratamentos foram de seis concentrações do fertilizante (0; 0,5; 1; 1,5; 2 e 2,5 g L-1) e um controle constituído de 1,9 g L-1 de reagente KNO3, conforme mostrado nos sais MS. Avaliou-se a sobrevivência, tamanho e número de brotações do explante, e o valor da biomassa fresca. Após a aclimatização das mudas avaliou-se a sobrevivência, número de brotações, comprimento da parte aérea, número de raízes, formação da raquete, massa média da biomassa fresca, absorção de macronutrientes e alterações morfológicas das mudas. Os explantes inoculados em meio com fertilizantes nas concentrações de 0,0; 2,0 e 2,5 g L-¹ não se desenvolveram. A resposta dos explantes nas concentrações de 0,5 e 1,5 g L-1 do fertilizante foram iguais aos desenvolvidos em meio contendo KNO3, e na concentração de 1,0 g L-1, em todas as variáveis, as médias foram superiores em relação as do controle. Dessa forma, constatou-se a viabilidade do uso do fertilizante no cultivo in vitro da palma, o que propiciou a eliminação dos entraves burocráticos e redução no custo de 99,12% na compra do produto.
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The aim of this study was to evaluate three plant species native to Caatinga (Aspidosperma pyrifolium, Ziziphus joazeiro and Pseudobombax simplicifolium) in response to inoculation with two arbuscular mycorrhizal fungi (autoctone: Claroideoglomus etunicatum or exotic: Acaulospora longula) and phosphate fertilization. The experiment was conducted in a greenhouse with a completely randomized design involving a factorial arrangement of three inoculation treatments (control, C. etunicatum or A. longula) and 4 levels of single superphosphate (0 - no added P2O5, 12, 24 and 48 mg dm-3) in 10 repetitions. Under the conditions of this study, the inoculum of C. etunicatum, autoctone to the semi-arid region, showed great compatibility and efficiency in promoting plant growth and nutrient intake when compared to the exotic inoculum of A. longula. Plants of A. pyrifolium were not responsive to mycorrhization and phosphate fertilization. In soil with low phosphorus content, mycorrhized plants of Z. joazeiro and P. simplicifolium presented better vegetative development with high shoot dry weight. Mycorrhized plants of Z. joazeiro had a proportional increase in the levels of macro- and micronutrients at the phosphorus doses applied. Mycorrhizal symbiosis may have a fundamental role in the development of these species from the Caatinga.
O objetivo do trabalho foi avaliar o desenvolvimento de três espécies vegetais nativas da Caatinga (Aspidosperma pyrifolium, Ziziphus joazeiro e Pseudobombax simplicifolium) em resposta à inoculação com dois fungos micorrízicos arbusculares (autóctone: Claroideoglomus etunicatum ou exótico: Acaulospora longula) e adubação fosfatada. O experimento foi realizado em casa de vegetação em delineamento inteiramente casualizado em arranjo fatorial com três tratamentos de inoculação (Controle, C. etunicatum ou A. longula) e quatro doses de superfosfato simples (0 - sem adição de P2O5, 12, 24 e 48 mg dm -3), em dez repetições. Nas condições deste estudo, o inóculo de C. etunicatum, autóctone da região semiárida, demonstrou maior compatibilidade e eficiência na promoção do crescimento e nutrição das plantas quando comparado ao inóculo exótico de A. longula. Plantas de A. pyrifolium não foram responsivas à micorrização e adubação fosfatada. Em solo com menor teor de fósforo as plantas de Z. joazeiro e P. simplicifolium micorrizadas apresentaram melhor desenvolvimento vegetativo, com elevada produção de biomassa seca da parte aérea. Plantas de Z. joazeiro micorrizadas tiveram aumento nos teores de macro e micronutrientes proporcional às doses de fósforo aplicadas. Conclui-se que simbiose micorrízica pode ter papel fundamental no desenvolvimento destas espécies nativas da Caatinga
Assuntos
Plantas , Zona Semiárida , Micorrizas , FungosRESUMO
The grasshopper species Orthoscapheus rufipes and Eujivarus fusiformis were analyzed using several cytogenetic techniques. The karyotype of O. rufipes, described here for the first time, had a diploid number of 2n = 23, whereas E. fusiformis had a karyotype with 2n = 21. The two species showed the same mechanism of sex determination (XO type) but differed in chromosome morphology. Pericentromeric blocks of constitutive heterochromatin (CH) were detected in the chromosome complement of both species. CMA3/DA/DAPI staining revealed CMA3-positive blocks in CH regions in four autosomal bivalents of O. rufipes and in two of E. fusiformis. The location of active NORs differed between the two species, occurring in bivalents M6 and S9 of O. rufipes and M6 and M7 of E. fusiformsi. The rDNA sites revealed by FISH coincided with the number and position of the active NORs detected by AgNO3 staining. The variability in chromosomal markers accounted for the karyotype differentiation observed in the tribe Abracrini.
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Euchroma gigantea was karyotypically studied using conventional staining, C-banding, silver nitrate staining and ribosomal fluorescent in situ hybridization (rDNA FISH). Broad wide autosomal polymorphism and a complex sex determination system were found in this beetle. Karyotype complements ranging from 2n = 32, X1X2X3Y1Y2Y3 to 2n = 36,X1X2X3Y1Y2Y3 were detected in the sample analyzed. Punctiform supernumerary chromosomes were present in the different karyotypes. The karyotypic evolution of Brazilian E. gigantea may have taken two directions, reduction in the diploid number of 2n = 36 to 24 through centric fusions or 2n = 24 to 36 due to chromosomal fissions. In addition, pericentric inversions were also involved. The complex multiple sex mechanism of this species seems to be old and well established since it is found in specimens from different populations. Small pericentromeric blocks of constitutive heterochromatin were located on the autosomes and terminal blocks were also found on some small pairs. The sex chromosomes showed larger constitutive heterochromatin blocks. Silver nitrate staining during prophase I of meiosis showed labeling of the sex chromosome chain. However, the rDNA sites could only be precisely determined by FISH, which permitted the identification of these ribosomal sites on chromosomes X1 and X2 of this species.
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Chromosome analyses were performed in two grasshopper species of the genus Schistocerca, S. pallens and S. flavofasciata. Both species shared the same diploid number (2n = 23, X in males; 2n = 24, XX in females);and a conserved karyotype composed exclusively of acrocentric chromosomes, but differed in their distribution patterns of constitutive heterochromatin and nucleolus organizer regions (NORs). Constitutive heterochromatin was located in the pericentromeric region of all chromosomes in both species. S. flavofasciata presented an additional C-band on the distal region of the long arm of a small autosome pair (S9). Nucleolus organizer regions (NORs), revealed by silver nitrate staining (Ag-NORs), were observed on a medium autosome pair (M5) in both species. S. pallens presented an additional NOR-bearing autosome (M6). The same sites were labeled after FISH with an rDNA probe in S. pallens cells.