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Incorporating different proportions of exotic maize germplasm into two adapted populations

Incorporating different proportions of exotic maize germplasm into two adapted populations

... were two adapted maize populations (BR 105 and BR 106) and six exotic germplasm sources (Acre 081 (AC), Amarillo 8 hileras (AO), Bolivia I-Moroti Precoce (BO), Colorado Perga- ... See full document

8

DIALLEL CROSSING AMONG MAIZE POPULATIONS FOR RESISTANCE TO FALL ARMYWORM

DIALLEL CROSSING AMONG MAIZE POPULATIONS FOR RESISTANCE TO FALL ARMYWORM

... potential of different materials are usually studied in controlled crosses; in this sense, the diallel mating scheme has been useful and largely used to estimate the potential value of genotypes per ... See full document

11

Heterosis and combining ability in crosses between two groups of open-pollinated maize populations

Heterosis and combining ability in crosses between two groups of open-pollinated maize populations

... variability of important traits, neither on the expression of agronomic traits at the population ...the exotic populations, previously selected for important leaf diseases, have now a chance ... See full document

9

Allozyme comparison of two populations of Rineloricaria (Siluriformes,

Allozyme comparison of two populations of Rineloricaria (Siluriformes,

... morphotypes of the genus Rinelocaria were compared through the allozyme electrophoresis tech- nique: one morphotype, ...stretch of the Ivaí River basin and the other, ...portion of the Ivaí River ... See full document

5

60,000 years of interactions between Central and Eastern Africa documented by major African mitochondrial haplogroup L2

60,000 years of interactions between Central and Eastern Africa documented by major African mitochondrial haplogroup L2

... splits into an Eastern African sub-clade (L2a1d1) at ...evidence of an early migration into Eastern Africa, like L2a1h and ...Bantu-speaking populations in the South and, although they were ... See full document

13

Genetic control of resistance to gray leaf spot of maize in tropical germplasm

Genetic control of resistance to gray leaf spot of maize in tropical germplasm

... identification of predominance of the additive effects and high heritability estimates, it becomes clear that the chances of obtaining GLS-resistant lines by selection are ...advantage of the ... See full document

6

Braz. j. oceanogr.  vol.53 número12

Braz. j. oceanogr. vol.53 número12

... effects of tributyltin (TBT) and triphenyltin (TPT), used as biocides in antifouling paints, as defensives fungicides or present in industrial effluents, on aquatic organisms are well known (Fent, 1996) and has ... See full document

3

Mutation load and the extinction of large populations

Mutation load and the extinction of large populations

... Evolution of the population for selfing Self=1 populations without recombination obtained for different initial populations and different environmental carrying capaci[r] ... See full document

18

Testing the link between genome size and growth rate in maize

Testing the link between genome size and growth rate in maize

... understanding of intra-species genome dynamics is essential for elucidating the diversification of GS among related ...species. Maize is an attractive model to test whether GS is fine-tuned by ... See full document

14

A comparative genetic diversity assessment of industrial and household Brazilian cassava varieties using SSR markers

A comparative genetic diversity assessment of industrial and household Brazilian cassava varieties using SSR markers

... types of cassava ...the two groups (va- rieties for industrial use and household consumption), indicating no genetic vulnerability in the cassava grown in the South Central region of ...number ... See full document

8

Sex ratio and dynamic behavior in populations of the exotic blowfly

Sex ratio and dynamic behavior in populations of the exotic blowfly

... blowfly populations, which should be considered in discrete models, such as delayed and function den- sity ...dynamics of fly populations since it fo- cuses on this ...dynamics of Drosophila ... See full document

8

Modeling of Two-Stage Solidification: Part II Computational Verification of the Model

Modeling of Two-Stage Solidification: Part II Computational Verification of the Model

... stage of solidification is the same for both modified and unmodified ...stage of the solidification, the nucleation process unfolds in slightly different way, depending on the eutectic transformation ... See full document

6

Isoenzymatic variation in the germplasm of Brazilian races of maize (Zea mays L.)

Isoenzymatic variation in the germplasm of Brazilian races of maize (Zea mays L.)

... number of allele/locus for the Mexican maize study would be 6, ...quency of allele Idh1-3 in population BRA 017574 (Table II) and its low frequency in two other populations (RGS XX and ... See full document

6

Egg Predation by the Introduced Lady Beetle, Coccinella septempunctata (Coleoptera: Coccinellidae), Lowers Mortality but Raises Relative Risk for the Native Lady Beetle, Coccinella novemnotata.

Egg Predation by the Introduced Lady Beetle, Coccinella septempunctata (Coleoptera: Coccinellidae), Lowers Mortality but Raises Relative Risk for the Native Lady Beetle, Coccinella novemnotata.

... Consumption of “trophic eggs” can increase fitness by recycling scarce resources and coccinellids have recently been the first non-eusocial insect taxon that demonstrates trophic egg plasticity in response to ... See full document

10

Genetic parameter and correlation estimates of processing traits in half-sib progenies of tropical-adapted carrot germplasm

Genetic parameter and correlation estimates of processing traits in half-sib progenies of tropical-adapted carrot germplasm

... areas of the world (Simon et al., 2008). However, most of the nutritionally improved carrot breeding materials developed in the Northern Hemisphere have poor adaptation to high temperatures and low soil ... See full document

5

Phenotypic diversity of basic characteristics of genotypes from the Serbia onion collection

Phenotypic diversity of basic characteristics of genotypes from the Serbia onion collection

... accessions of different origins were studied in the paper (Table ...Sixteen of them are populations and fourteen varieties. Twelve of the genotypes originate from Serbia (No 1-12), six ... See full document

8

J. Bras. Patol. Med. Lab.  vol.50 número2

J. Bras. Patol. Med. Lab. vol.50 número2

... analysis of variables for the characterization of control groups and patients was carried out, and the frequency of PNH cells was ...comparison of PNH clone sizes detected in neutrophils and ... See full document

10

J. Braz. Chem. Soc.  vol.12 número3

J. Braz. Chem. Soc. vol.12 número3

... chemistry of different populations of two Brazilian Viguiera species has been performed by the glandular trichome microsampling technique and isocratic HPLC ...pattern of all ... See full document

5

Genetic parameter estimates and identification of superior white maize populations

Genetic parameter estimates and identification of superior white maize populations

... shortage of white maize cultivars and genetic studies for special maize breeding ...identify populations and promising hybrid white maize for main agronomic traits and grits processing ... See full document

8

O uso de diferentes espécies na arborização de ruas e seu efeito para o conforto...

O uso de diferentes espécies na arborização de ruas e seu efeito para o conforto...

... loss of environmental quality, such as the lack of trees in the ...the different environmental conditions between a street with and without trees in a ...management of the trees can benefit ... See full document

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