Gate fidelity of arbitrary single-qubit gates constrained by conservation laws

Recent investigations show that conservation laws limit the accuracy of gate operations in quantum computing. The inevitable error under the angular momentum conservation law has been evaluated so far for the CNOT, Hadamard, and NOT gates for spin 1/2 qubits, while the SWAP gate has no constraint. Here, we extend the above results to general single-qubit gates. We obtain an upper bound of the gate fidelity of arbitrary single-qubit gates implemented under arbitrary conservation laws, determined by the geometry of the conservation law and the gate operation on the Bloch sphere as well as the size of the ancilla.Comment: Title changed; to appear in J. Phys. A: Math. Theor.; 19 pages, 2 figure

Regeneração de Passiflora suberosa em suspensão celular.

O gênero Passiflora é o maior e o mais importante da família Passifloraceae por abrigar as principais espécies exploradas comercialmente no mundo. Muitas espécies são cultivadas para a produção de sucos, consumo in natura, extração de substâncias de interesse farmacológico e fins ornamentais, mas a presença de patógenos de solo que vêm dizimando os cultivos. Uma alternativa é a hibridação interespecífica, ou seja, cruzamentos convencionais, de seleção ou cultivares comerciais, com as espécies silvestres na produção de porta-enxertos resistentes, porém esses híbridos sexuais quando obtidos têm apresentado baixa fertilidade. Desta forma, uma alternativa viável é a produção de porta-enxertos tetraplóides com genes de resistência aos patógenos pela técnica da hibridação somática. Contudo, para isto são necessários protocolos eficientes de regeneração das espécies parentais diplóides a patir de células individuais. Assim, o objetivo desse trabalho foi estabelecer um protocolo de regeneração de plantas a partir de células em suspensão da espécie de P. suberosa. Para tanto, calos MR13 BIO oriundos da Embrapa de Mandioca e Fruticultura Tropical de Cruz das Almas/BA foram submetidos ao meio de cultura MS (Murashige e Skoog) suplementado com os reguladores de crescimento BAP 1,0 mg/L ou 2,0 mg/L; KIN 1,0 mg/L ou 2,0 mg/L para a obtenção de calos friáveis no Laboratório de Cultura de Tecidos Vegetais da unidade experimental Horto Florestal da Universidade Estadual de Feira de Santana/BA. O melhor resultado, BAP 2,0 mg/L, foi submetido aos testes contendo balanço de fitorreguladores: MS + BAP 2,0 mg/L + ANA 0,5 mg/L + Kin 1,0 mg/L ou MS + AIA 2,5 mg/L + ANA 0,5 mg/L +Kin 1,0 mg/L, suplementado com agar 6% e, ao teste de culturas de células em suspensão, na ausência de luz, em meio MS na metade da concentração dos sais, suplementados pelos compostos orgânicos (extrato de malte ou extrato de levedura) e mantidos sob 140 rpm de agitação contínua num volume final de 100 mL em frascos erlenmeyers de 250 mL de capacidade. As células colocadas em suspensão no meio líquido suplementado com extrato de malte foram capazes de regenerar de plantas inteiras de P. suberosa, a partir de células diplóides, num prazo de 60 dias na ausência de luz.Disponível em: Acesso em: 02 mar. 201

Satellite DNA in Paphiopedilum subgenus Parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization

Background: Satellite DNA is a rapidly diverging, largely repetitive DNA component of many eukaryotic genomes. Here we analyse the evolutionary dynamics of a satellite DNA repeat in the genomes of a group of Asian subtropical lady slipper orchids (Paphiopedilum subgenus Parvisepalum and representative species in the other subgenera/sections across the genus). A new satellite repeat in Paphiopedilum subgenus Parvisepalum, SatA, was identified and characterized using the RepeatExplorer pipeline in HiSeq Illumina reads from P. armeniacum (2n = 26). Reconstructed monomers were used to design a satellite-specific fluorescent in situ hybridization (FISH) probe. The data were also analysed within a phylogenetic framework built using the internal transcribed spacer (ITS) sequences of 45S nuclear ribosomal DNA. Results: SatA comprises c. 14.5% of the P. armeniacum genome and is specific to subgenus Parvisepalum. It is composed of four primary monomers that range from 230 to 359 bp and contains multiple inverted repeat regions with hairpin loop motifs. A new karyotype of P. vietnamense (2n = 28) is presented and shows that the chromosome number in subgenus Parvisepalum is not conserved at 2n = 26, as previously reported. The physical locations of SatA sequences were visualised on the chromosomes of all seven Paphiopedilum species of subgenus Parvisepalum (2n = 26–28), together with the 5S and 45S rDNA loci using FISH. The SatA repeats were predominantly localisedin the centromeric, peri-centromeric and sub-telocentric chromosome regions, but the exact distribution pattern was species-specific. Conclusions: We conclude that the newly discovered, highly abundant and rapidly evolving satellite sequence SatA is specific to Paphiopedilum subgenus Parvisepalum. SatA and rDNA chromosomal distributions are characteristic of species, and comparisons between species reveal that the distribution patterns generate a strong phylogenetic signal. We also conclude that the ancestral chromosome number of subgenus Parvisepalum and indeed of all Paphiopedilum could be either 2n = 26 or 28, if P. vietnamense is sister to all species in the subgenus as suggested by the ITS data

Fontes de resistência de videira ao fungo oídio no Nordeste brasileiro.

Foram avaliadas 135 variedades distintas em três ciclos, observando-se as mesmas plantas sem nenhum oídicida

In Vitro Propagation of \u3ci\u3ePennisetum purpureum\u3c/i\u3e Schum.

A protocol is described for rapid multiplication of elephantgrass (Pennisetum purpureum Schum.) through shoot tip culture. The plant growth medium consisted of basal medium of Murashige and Skoog (MS) and vitamins Wood Plant Medium (WPM). The medium was supplemented with 0.00; 4.44; 8.88; 13.32 and 17.76 μM of benzylaminopurine (BAP). The elephantgrass was micropropagated by axillary shoot proliferations. Maximum propagule proliferation occurred on Murashige and Skoog (MS) medium enriched with 4.4 μM benzylaminopurine (BAP), resulting an average of 4.0 shoots per explant from cultivar Mineiro and 2.19 from cultivar Pioneiro. The best height and root plantlets were obtained with medium without growth regulator after 28 days

Orthorhombic Phase of Crystalline Polyethylene: A Constant Pressure Path Integral Monte Carlo Study

In this paper we present a Path Integral Monte Carlo (PIMC) simulation of the orthorhombic phase of crystalline polyethylene, using an explicit atom force field with unconstrained bond lengths and angles. This work represents a quantum extension of our recent classical simulation (J. Chem. Phys. 106, 8918 (1997)). It is aimed both at exploring the applicability of the PIMC method on such polymer crystal systems, as well as on a detailed assessment of the importance of quantum effects on different quantities. We used the $NpT$ ensemble and simulated the system at zero pressure in the temperature range 25 - 300 K, using Trotter numbers between 12 and 144. In order to investigate finite-size effects, we used chains of two different lengths, C_12 and C_24, corresponding to the total number of atoms in the super-cell being 432 and 864, respectively. We show here the results for structural parameters, like the orthorhombic lattice constants a,b,c, and also fluctuations of internal parameters of the chains, such as bond lengths and bond and torsional angles. We have also determined the internal energy and diagonal elastic constants c_11, c_22 and c_33. We discuss the temperature dependence of the measured quantities and compare to that obtained from the classical simulation. For some quantities, we discuss the way they are related to the torsional angle fluctuation. In case of the lattice parameters we compare our results to those obtained from other theoretical approaches as well as to some available experimental data. In order to study isotope effects, we simulated also a deuterated polyethylene crystal at a low temperature. We also suggest possible ways of extending this study and present some general considerations concerning modeling of polymer crystals.Comment: 18 pages, RevTex, 18 figures, 3 tables, submitted to Phys. Rev.

Seleção molecular assistida para identificação de alelo para cor rósea na cultivar Brisa IPA 12.

O objetivo do presente trabalho foi aplicar os marcadores moleculares ANS para genotipar 270 plantas da Brisa IPA 12 que segregavam para bulbos de cor rósea, que podem ficar ?escondidos? nas plantas heterozigotas, de forma a eliminar essa condição que dificulta a aceitação comercial dessa cultivar de cebola. DNA total foi extraído conforme protocolo CTAB 2x, de amostras foliares de plantas coletadas aos 30 dias após a semeadura dos bulbos vernalizados e pré-selecionados para a cor amarelaSuplemento. Edição dos Anais do 53 Congresso Brasileiro de Olericultura, jul. 2014

The effect of matured date palm tree ( Phoenix dactylifera

The effect of a hot water extract of matured date palm tree fruit on allergic responses was investigated in NC/Nga mice. The allergic score was significantly reduced in the mice fed a date palm tree fruit extract-added diet than the fruit extract-free diet. The levels of serum antigen-specific immunoglobulin E and spleen interleukin (IL)-4+CD4+ cells were significantly lowered in the mice fed the fruit extract-added diet. Bruton's tyrosine kinase (Btk) and IL-2-inducible T cell kinase (Itk) mRNA expressions in spleen cells were significantly lowered in the mice fed the fruit extract-added diet. Moreover, chlorogenic acid and pelargonin decreased these mRNA expressions in C3H/HeN mouse spleen cell cultures. These results suggest that the date palm tree fruit extract may reduce allergic symptoms in mice via a decrease in the number of type 2 helper T (Th2) cells, and a suppression of the expression of kinases involved in mast cell degranulation and Th2 cell differentiation.ArticleFOOD AND AGRICULTURAL IMMUNOLOGY. 25(1):49-60 (2014)journal articl

Techniques for Arbuscular Mycorrhiza Inoculum Reduction

It is well established that arbuscular mycorrhizal (AM) fungi can play a significant role in sustainable crop production and environmental conservation. With the increasing awareness of the ecological significance of mycorrhizas and their diversity, research needs to be directed away from simple records of their occurrence or casual speculation of their function (Smith and Read 1997). Rather, the need is for empirical studies and investigations of the quantitative aspects of the distribution of different types and their contribution to the function of ecosystems. There is no such thing as a fungal effect or a plant effect, but there is an interaction between both symbionts. This results from the AM fungi and plant community size and structure, soil and climatic conditions, and the interplay between all these factors (Kahiluoto et al. 2000). Consequently, it is readily understood that it is the problems associated with methodology that limit our understanding of the functioning and effects of AM fungi within field communities. Given the ubiquous presence of AM fungi, a major constraint to the evaluation of the activity of AM colonisation has been the need to account for the indigenous soil native inoculum. This has to be controlled (i.e. reduced or eliminated) if we are to obtain a true control treatment for analysis of arbuscular mycorrhizas in natural substrates. There are various procedures possible for achieving such an objective, and the purpose of this chapter is to provide details of a number of techniques and present some evaluation of their advantages and disadvantages. Although there have been a large number of experiments to investigated the effectiveness of different sterilization procedures for reducing pathogenic soil fungi, little information is available on their impact on beneficial organisms such as AM fungi. Furthermore, some of the techniques have been shown to affect physical and chemical soil characteristics as well as eliminate soil microorganisms that can interfere with the development of mycorrhizas, and this creates difficulties in the interpretation of results simply in terms of possible mycorrhizal activity. An important subject is the differentiation of methods that involve sterilization from those focussed on indigenous inoculum reduction. Soil sterilization aims to destroy or eliminate microbial cells while maintaining the existing chemical and physical characteristics of the soil (Wolf and Skipper 1994). Consequently, it is often used for experiments focussed on specific AM fungi, or to establish a negative control in some other types of study. In contrast, the purpose of inoculum reduction techniques is to create a perturbation that will interfere with mycorrhizal formation, although not necessarily eliminating any component group within the inoculum. Such an approach allows the establishment of different degrees of mycorrhizal formation between treatments and the study of relative effects. Frequently the basic techniques used to achieve complete sterilization or just an inoculum reduction may be similar but the desired outcome is accomplished by adjustments of the dosage or intensity of the treatment. The ultimate choice of methodology for establishing an adequate non-mycorrhizal control depends on the design of the particular experiments, the facilities available and the amount of soil requiring treatment