Structure and cytochemistry of the pistil in Arachis hypogaea

In Arachis hypogaea (Papilionoideae, Leguminosae), the stigma is of the dry papillate type. The papillae are multicellular and multiseriate. They are covered with a thin lining of pellicle which responds for proteins, non-specific esterases and acid phosphatases. The style is 3-6 cm long and hollow throughout its length. The stylar canal is bordered by a layer of canal cells. The canal cells in most of the stylar region are not glandular, they are vacuolate with scant cytoplasm. The canal cells at the base of the style, however, are glandular with dense cytoplasm and prominent nuclei. The structural features of the pistil of Arachis are discussed with those of other Papilionoideae

The minimum mean monopoly energy of a graph

The motivation for the study of the graph energy comes from chemistry, where the research on the so-called total pi - electron energy can be traced back until the 1930s. This graph invariant is very closely connected to a chemical quantity known as the total pi - electron energy of conjugated hydro carbon molecules. In recent times analogous energies are being considered, based on Eigen values of a variety of other graph matrices. In 1978, I.Gutman [1] defined energy mathematically for all graphs. Energy of graphs has many mathematical properties which are being investigated. The ordinary energy of an undirected simple finite graph G is defined as the sum of the absolute values of the Eigen values of its associated matrix. i.e. if mu(1), mu(2), ..., mu(n) are the Eigen values of adjacency matrix A(G), then energy of graph is Sigma(G) = Sigma(n)(i=1) vertical bar mu(i)vertical bar Laura Buggy, Amalia Culiuc, Katelyn Mccall and Duyguyen [9] introduced the more general M-energy or Mean Energy of G is then defined as E-M (G) = Sigma(n)(i=1)vertical bar mu(i) - (mu) over bar vertical bar, where (mu) over bar vertical bar is the average of mu(1), mu(2), ..., mu(n). A subset M subset of V (G), in a graph G (V, E), is called a monopoly set of G if every vertex v is an element of (V - M) has at least d(v)/2 neighbors in M. The minimum cardinality of a monopoly set among all monopoly sets in G is called the monopoly size of G, denoted by mo(G) Ahmed Mohammed Naji and N.D.Soner [7] introduced minimum monopoly energy E-MM [G] of a graph G. In this paper we are introducing the minimum mean monopoly energy, denoted by E-MM(M) (G), of a graph G and computed minimum monopoly energies of some standard graphs. Upper and lower bounds for E-MM(M) (G)are also established.Publisher's Versio

Maximizing Red Gram yield through Integrated Agronomic Management Practices under alkali soil

Abstract Th

A Secure and authorized Duplication model in Cloud Using multi-layered cryptosystem based

the present a scheme that permits a more fine-grained trade-off. The intuition is that outsourced data may require different levels of the protection, depending on how to popular it is: content shared by many users, such as popular song or video, arguably requires less protection than a personal document, the copy of a payslip or the draft of an un submitted scientific paper. Unfortunately, semantically secure encryption schemes render various cost-effective storage optimization techniques, such as the data de duplication, ineffective. We present a novel idea that differentiates data according to their popularity. Based on this idea, we design an encryption scheme that the guarantees semantic security for the unpopular data and provides weaker security and better storage and bandwidth benefits for popular data

UPLC SEPARATION ANALYSIS OF EMTRICITABINE, TENOFOVIR, COBICISTAT AND ELVITEGRAVIR FROM THEIR DEGRADATION PRODUCTS

Objective: A simple, rapid, accurate and precise stability-indicating UPLC analytical method has been developed and validated for the quantitative analysis of Emtricitabine, Tenofovir, Cobicistat and Elvitegravir in bulk drugs and combined dosage forms.Methods: ACE C18 (50 mm x 3 mm, 2µ). The column temperature was maintained at 30oC and run time 8 min. The mobile phase was a mixture of Mobile Phase: A–0.1% TFA in Acetonitrile, B–0.1% TFA in Milli-Q-water. The injection volume of samples was 20μl. UV detection was carried out using a UV-PDA detector at 240 nm. The validation of this method was done as per ICH guidelines.Results: The retention times were observed as 1.46, 3.59, 4.13, 4.64 min for Emtricitabine, Tenofovir disoproxyl fumarate, Cobicistat, and Elvitegravir respectively. Linearity ranges were observed 150-275 µg/ml Emtricitabine, 250-375 µg/ml Tenofovir, 100-225 µg/ml Cobicistat and 100-225 µg/ml Elvitegravir. Relative Standard Deviation did not exceed 2.Conclusion: The newly developed UPLC method for separation of different degradation products along with the pure drugs were found to be capable of giving faster retention times while still maintaining good resolution than that achieved with conventional HPLC. The decreased flow rate 0.4 ml/min, in UPLC indicate more economical. This method exhibited an excellent performance in terms of sensitivity and speed. The results of stress testing undertaken according to the ICH guidelines reveal that the method is specific and stability-indicating. The proposed method has the ability to separate these drugs from their degradation products in tablet dosage forms and hence can be applied to the analysis of routine quality control samples and samples obtained from stability studies.Keywords: Stability indicating assay, RP-UPLC, Emtricitabine, Tenofovir, Cobicistat, Elvitegravir, Forced degradation studie

Genome-Wide Differentiation of Various Melon Horticultural Groups for Use in GWAS for Fruit Firmness and Construction of a High Resolution Genetic Map

Ajuts: Funding support is provided by Gus R. Douglass Institute (Evans Allen Project to Nimmakayala) and USDA-NIFA (2010-02247 and 2012-02511).Melon (Cucumis melo L.) is a phenotypically diverse eudicot diploid (2n = 2x = 24) has climacteric and non-climacteric morphotypes and show wide variation for fruit firmness, an important trait for transportation and shelf life. We generated 13,789 SNP markers using genotyping-by-sequencing (GBS) and anchored them to chromosomes to understand genome-wide fixation indices (Fst) between various melon morphotypes and genomewide linkage disequilibrium (LD) decay. The FST between accessions of cantalupensis and inodorus was 0.23. The FST between cantalupensis and various agrestis accessions was in a range of 0.19-0.53 and between inodorus and agrestis accessions was in a range of 0.21-0.59 indicating sporadic to wide ranging introgression. The EM (Expectation Maximization) algorithm was used for estimation of 1436 haplotypes. Average genome-wide LD decay for the melon genome was noted to be 9.27 Kb. In the current research, we focused on the genome-wide divergence underlying diverse melon horticultural groups. A high-resolution genetic map with 7153 loci was constructed. Genome-wide segregation distortion and recombination rate across various chromosomes were characterized. Melon has climacteric and non-climacteric morphotypes and wide variation for fruit firmness, a very important trait for transportation and shelf life. Various levels of QTLs were identified with high to moderate stringency and linked to fruit firmness using both genome-wide association study (GWAS) and biparental mapping. Gene annotation revealed some of the SNPs are located in β-D-xylosidase, glyoxysomal malate synthase, chloroplastic anthranilate phosphoribosyltransferase, and histidine kinase, the genes that were previously characterized for fruit ripening and softening in other crops

Epidemiology and patterns of care for invasive breast carcinoma at a community hospital in Southern India

<p>Abstract</p> <p>Background</p> <p>Breast cancer incidence in India is on rise. We report epidemiological, clinical and survival patterns of breast cancer patients from community perspective.</p> <p>Methods</p> <p>All breast cancer patients treated at this hospital from July 2000 to July 2005 were included. All had cytological or histological confirmation of breast cancer. TNM guidelines for staging and Immunohistochemistry to assess the receptor status were used. Either lumpectomy with axillary lymph node dissection or Modified radical mastectomy (MRM) was done for operable breast cancer, followed by 6 cycles of adjuvant chemotherapy with FAC or CMF regimens to patients with pT >1 cm or lymph node positive or estrogen receptor negative and radiotherapy to patients after breast conservation surgery, pT size > 5 cm, 4 or more positive nodes and stage IIIB disease. Patients with positive Estrogen receptor or Progesterone receptor were advised Tamoxifene 20 mg per day for 3 years. Descriptive analysis was performed. Independent T test and Chi-square test were used. Overall survival time was computed by Kaplan – Meier method.</p> <p>Results</p> <p>Of 1488 cancer patients, 122 (8.2%) had breast cancer. Of 122 patients, 96.7% had invasive breast carcinoma and 3.3% had sarcoma. 94% came from the rural and semi urban areas. Premenopausal women were 27%. The median age was 50 years. Stage I-6.8%, II-45.8%, III-22%, IV-6.8%, Bilateral breast cancer – 2.5%. The mean pT size was 3.9 cm. ER and PR were positive in 31.6% and 28.1% respectively. MRM was done in 93.8%, while 6.3% patients underwent breast conservation surgery. The mean of the lymph nodes dissected were 3. CMF and FAC regimens were used in 48.8% and 51.2% of patients respectively. FAC group were younger than the CMF group (43.6 yr vs. 54 yrs, P = 0.000). Toxicities were more in FAC than CMF group, alopecia (100% vs. 26.2%), grade2 or more emesis (31.8% vs. 9.2%), grade2 or more fatigue (40.9% vs.19%), anemia (43.1% vs. 16.6%). Median Survival for the cohort was 50.8 months. ER positive patients had better median survival (P = 0.05).</p> <p>Conclusion</p> <p>MRM was the most frequent surgical option. CMF and FAC showed equivalent survival. FAC chemotherapy was more toxic than CMF. ER positive tumors have superior survival. Overall 3 year survival was 70 percent</p