Quantifying the detrimental effect of airborne dust on herbicide efficacy

One side effect of human activity and global climatic change is more airborne dust. This not only has undesirable effects on human health and the environment, but may also adversely affect many agricultural processes, including herbicide efficacy. This is particularly relevant in parts of the world where dust storms are common and limited rainfall means dust persists on plants for protracted periods. Accordingly, a series of greenhouse dose–response pot experiments was carried out to quantify the effect of a dust concentration of 1,500 µg/m³ on the performance of paraquat, glyphosate, sulfosulfuron and 2,4-D+MCPA. Dust-treated and untreated seedlings of Hordeum spontaneum and Sinapis arvensis were sprayed with sulfosulfuron and 2,4-D+MCPA, respectively, while paraquat and glyphosate were applied to both weed species. The efficacy of glyphosate and paraquat decreased significantly in the presence of dust on both species. Similar results were observed for 2,4-D+MCPA on S. arvensis. In contrast, the efficacy of sulfosulfuron on H. spontaneum was not affected by dust. In the presence of dust, the doses of glyphosate, paraquat and 2,4-D+MCPA required for a 90% effect were enhanced by a factor of 1.9 to 2.6. The negative impact on glyphosate efficacy was more pronounced in S. arvensis than H. spontaneum, while it was similar for paraquat. Future studies should consider the amount, duration and composition of dust as well as its impact on other weeds and herbicides. Potential approaches to overcome the detrimental influence of dust on the performance of herbicides were also suggested for future studies.     

Influence of Ascophyllum nodosum algae extract on finishing growth performance and nutrient digestibility of buffalo calves in warm climates

Tropical Animal Health and Production - The present experiment was conducted to investigate the effect of using an extract of Ascophyllum nodosum algae (Tasco®, AN) on feed digestibility and...     

Age-Specific Gastric Cancer Risk Indicated by the Combination of Helicobacter pylori Sero-Status and Serum Pepsinogen Levels

Background:

Serologic screening of gastric cancer (GC) by serum pepsinogens (sPG) levels and Helicobacter pylori (Hp) sero-status, though highly informative, has provided heterogeneous results. Here, we have evaluated the modifying effects of demographic factors on the risk impact of Hp sero-status/sPG levels in gastric cancer, with particular emphasis on age.

Methods:

A cross-sectional study was carried out on 1341 individuals (GC = 578, healthy = 763), who were stratified into two age groups: 35-59 years (middle-aged, n = 830) and ≥ 60 years (60 years-plus, n = 511). Demographic factors and serological states (Hp sero-staus and sPG levels) were recorded by subject interview and serum ELISAs, respectively. Covariate-specific odds ratios were calculated by multivariable logistic regression.

Results:

Hp infection was consistently associated with increased sPGI and sPGII levels in the 60 year-plus, but not the middle-aged group. The joint examination of the variable states of the three serum biomarkers (Hp serology, sPGI, and sPGI/II ratio), in the 60 year-plus age group, demonstrated a stepwise escalation of risk from the single (sPGI_low; OR = 2.6), to double (sPGI_low/sPGI/II_low; OR = 3.55, and Hp_positive/sPGI_low; OR = 5.0) and ultimately triple (Hp_positive/PGI_low/PGI/II_low; OR = 10.48) positive states, in reference to the triple negatives. However, this pattern was not exhibited in the middle-aged subjects.

Conclusion:

Age was clearly identified as a modifying factor on the risk projection of the combined states of Hp serology and sPG levels in gastric cancer screening, reflected by the augmented (~10.5 fold) risk of GC in the triple positive (Hp_positive/sPGI_low/sPGI/II_low) 60 year-plus subjects, which was not evident in the middle-aged group. Key Words: Biomarkers, Demography, Age Distribution     

Impact of Methylenetetrahydrofolate Reductase C677T Polymorphism on the Risk of Gastric Cancer and Its Interaction with Helicobacter pylori Infection

Background

Attempts for early detection of gastric cancer have recently focused on host''s genetic susceptibility factors and gene-environment interactions. We have, herein, studied the association of MTHFR C677T single nucleotide polymorphism (SNP) and its interaction with Helicobacter pylori infection, smoking, age and gender on the risk of gastric cancer among an Iranian population.

Methods

Gastric cancer patients (n = 450) and cancer-free controls (n = 780) were studied for serum H. pylori-specific IgG antibodies by ELISA and MTHFR C677T polymorphism (SNP) by PCR-RFLP. Demographic and life style data were collected through patient interviews. Unconditional logistic regression model estimated odds ratio (OR) and the corresponding 95% confidence intervals (CI).

Results

The interactions of MTHFR genotype with H. pylori infection (P = 0.03), age (P = 0.049) and gender (P = 0.007) were statistically significant. Accordingly, MTHFR C677T carriers who were also positive for H. pylori infection exhibited 80% (OR = 1.8, 95% CI = 1.0-2.9) significant excess risk of non-cardia gastric cancer. Furthermore, subjects over the age of 50 or female subjects carrying MTHFR C677T SNP showed 40 (OR = 1.4, 95% CI = 1.0-2.0) and 100 (OR = 2.0, 95% CI = 1.2-3.2) percent increased risk of gastric cancer, respectively.

Conclusion

MTHFR C677T SNP seems to increase the risk of gastric cancer and the effect is significantly inflated by interactions with H. pylori infection, age and gender. Key Words: Helicobacter pylori, Smoking, Gender identity, Age group, Methylenetetrahydrofolate reductase     

Evaluation of various hCG treatment strategies applied to domesticated pikeperch (Sander lucioperca) broodstock on nest-spawning performance

The aim of the present study was to evaluate the effects of hCG injections on reproductive efficiency by hCG treatment in both male or female brooders of domesticated pikeperch (Sander lucioperca) in the first generation. The study consisted of four treatments based on hormone injection to male or female brooders including T1: both sexes were injected, T2: only females were injected, T3: only males were injected, and T4: without hormone injection. Each treatment which included 14 males and 12 females were introduced to a single rectangular concrete tank with one spawning nest for each mate (a total of 12 nests per tank). Fish were injected by a single dose of 200 IU/kg hCG before transferring to mating tanks. After mating, nests containing fertilized eggs were transferred to circular concrete tanks for incubation and hatching of embryos. According to the results, treatments T3 and T4 did not respond to hormonal stimulation and no fish were spawned. Treatments T1 and T2 showed a positive response to hormone injection. Latency time, fertilization rate, and hatching rate showed no significant difference between T1 and T2 (P?>?0.05), but the number of responded females was significantly higher in T2 (P?<?0.05). The results of the present study demonstrated that it is possible to perform the semi-artificial propagation of domesticated pikeperch via injecting with 200 IU/kg hCG just to females, without the need for hormonal stimulation for males.

     

Mitochondrial DNA Copy Number Variations and Serum Pepsinogen Levels for Risk Assessment in Gastric Cancer

Background:Variations in mtDNA-CN of PBLs, as a potential biomarker for GC screening has currently been subject to controversy. Herein, we have assessed its efficiency in GC screening, in parallel and in combination with sPG I/II ratio, as an established indicator of gastric atrophy. Methods:The study population included GC (n = 53) and non-GC (n = 207) dyspeptic patients. The non-GC group was histologically categorized into CG (n = 104) and NM (n = 103) subgroups. The MtDNA-CN of PBLs was measured by quantitative real-time PCR. The sPG I and II levels and anti-H. pylori serum IgG were measured by ELISA. Results:The mtDNA-CN was found significantly higher in GC vs. non-GC (OR = 3.0; 95% CI = 1.4, 6.4) subjects. Conversely, GC patients had significantly lower sPG I/II ratio than the non-GC (OR = 3.2; CI = 1.4, 7.2) subjects. The combination of these two biomarkers yielded a dramatic amplification of the odds of GC risk in double-positive (high mtDNA-CN-low sPGI/II) subjects, in reference to double-negatives (low mtDNA-CN-high sPGI/II), when assessed against non-GC (OR = 27.1; CI = 5.0, 147.3), CG (OR = 13.1; CI = 2.4, 72.6), or NM (OR = 49.5; CI = 7.9, 311.6) groups. Conclusion:The combination of these two biomarkers, namely mtDNA-CN in PBLs and serum PG I/II ratio, drastically enhanced the efficiency of GC risk assessment, which calls for further validations. Key Words: Biomarkers, DNA copy number variation, Mitochondrial DNA, Stomach neoplasms